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

LLGL2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs190525699	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75528394	TGCTGGGATTACAGG[C/T]GTAAGCCACCGCGCC	3993
rs190605708	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75560919	TCACTGCAACCTCTG[C/T]TTCCTGGGTTCAAGT	3993
rs190613484	snp	A/G	0.00274103	0.0369188	intron-variant	LLGL2	GRCh38.p7	17:75558507	CCGTCGTGTGCCCTC[A/G]CCAGTGCCAGCTGGT	3993
rs190628875	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523141	CCAAGATCACGCCAC[C/T]ATACTCCAGCCTGGG	3993
rs190761621	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546537	TTGAGGTTGAGTTGG[A/G]GGAGCCTTGGGACAG	3993
rs190837527	snp	A/G	0.000203943	0.010096	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571989	CGAGCCCCTCGAAGT[A/G]GCCCATGATCTGTCG	3993
rs190854216	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75553364	AGGCATCCCCCAAAA[C/T]AGGCACTTGTTGGAG	3993
rs190860223	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534404	CTGCGAGCAGGCAGC[C/T]CCTTTGTCCTGGGAG	3993
rs190874312	snp	C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75540145	TGTTGGCCCCTAGCC[C/T]AGGGCTCTTTCCCTT	3993
rs190986634	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530296	TTGCTTGAACCCAGG[A/G]GTTCAAGACCAGCCT	3993
rs191001490	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75538500	TCTCAGTGGAGACCT[C/T]GCCTCCTCTGTTCAT	3993
rs191107144	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530378	GGCATCAGCCAGGCG[C/T]GGTGTCTCACGCCTG	3993
rs191154714	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75547303	AGTTCACCGAGGGCT[A/G]TGTGCCAGGCATCAG	3993
rs191258281	snp	C/T	0.0260105	0.111035	intron-variant	LLGL2	GRCh38.p7	17:75572255	ACAGGGGGCCAGGCG[C/T]GGTGACTCATGCCTG	3993
rs191268691	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75534936	CTTAATTAACAACAG[C/T]GGGGACGACAGTCCT	3993
rs191378477	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75563658	ACAGGTCTACCATGT[A/G]GATGTGGCATGAGCT	3993
rs191402673	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529448	GACTTCAAGTGATCT[G/T]CCTGCCTCAGCCTCT	3993
rs191410134	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524694	GAGAGGGTGCCTGCT[A/T]CGTGCTATAAAGCCA	3993
rs191421736	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552391	CTCCTCAGGAGGCTG[A/C]GGCGGGAGGATCACT	3993
rs191501508	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75553956	ATACTCAACAATAAA[C/T]CTCTGGTGAATTAGG	3993
rs191588690	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559789	TGGTGCCACCCTTTG[C/G]GGTGGGTACTTTGCT	3993
rs191590797	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542659	TCTCCACTAGGGCCC[A/G]TGGGAAAGAGAACCT	3993
rs191648099	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544522	CAGGTGCAAACCCAA[C/T]TTTGCCACATAGAAG	3993
rs191657471	snp	A/T	0.000134433	0.00819746	intron-variant	LLGL2	GRCh38.p7	17:75570325	AGGACCTAGCAGCAC[A/T]GACAGCCTGCCATCC	3993
rs191736619	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562166	CACCTCCAGCCCTCA[C/T]GGCAGCATTCCAGGC	3993
rs191751121	snp	C/T	0.00993419	0.0697739	intron-variant	LLGL2	GRCh38.p7	17:75545238	CCCAAACTTGATTGT[C/T]CCACTCCCAGGCCTG	3993
rs191752609	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527238	GAGGCACAAGGAGAA[C/T]TGTGCGAGAGATGTC	3993
rs191964220	snp	C/T	0.00557542	0.0525036	intron-variant	LLGL2	GRCh38.p7	17:75535744	CCCCACTGGTCTCTT[C/T]CTTGAGCTCTTGAGA	3993
rs192033141	snp	A/G	0.00284599	0.0376151	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564557	GGTGTGGGAGGCATG[A/G]GGCAGGACCATCAGT	3993
rs192342916	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554946	CTTGTAATCCTAGCA[C/T]TTTGGGAGGCTGAGG	3993
rs192392119	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547757	TTGAACCCTGGAGGC[A/G]GAGATTGCAGTGAGC	3993
rs192447204	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75574781	CGTGCCCTGATGACC[A/G]GGAAAGCACCATGTC	3993
rs192451173	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555642	TGCGGTGCAACCAAG[A/G]TTTTCTCCCGAGAGA	3993
rs192462717	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536817	GAAATGGTCTTTTCT[C/T]CATTTATTTATTTAT	3993
rs192508121	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559536	ATGGGGCTATAGCAG[A/G]GGAGGCTCTTGGCTT	3993
rs192559979	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549857	CACTCGCTCCCCTTC[C/T]GGGACCTGGAAAGGA	3993
rs192566153	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532057	ATATATGTATATATA[C/T]ACACACACACACACA	3993
rs192567592	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75559055	GGTCCCTGGCGTCTT[C/T]CCTGCCTCCTAGCCC	3993
rs192647311	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548563	CCAGCAGTTTGGGAG[A/G]CTGAGGCAGGTAGAT	3993
rs192725699	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575445	TCTGCCTGACTTTTT[C/T]CCTGGGTCCTGGCCG	3993
rs192812488	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542112	CAACTCTGCCACGCA[C/T]GTTACCTACCTTCTC	3993
rs192875101	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566566	GCCATTGCAGAGCAC[A/T]TGTAGCCATGGACAA	3993
rs192882349	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530767	AGTGAACTATGATGG[C/T]GCCACTGCACTCCAG	3993
rs192987000	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562719	GGTTATAGCCATGTG[C/T]CACCACGCCCAGCTA	3993
rs192999122	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75528298	TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC	3993
rs193071790	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75545112	AGGGCTGAACACCCC[C/T]CTACCCCTGCCCCCT	3993
rs193116958	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541778	TCTGTTGCCCAGGCC[A/G]GAGTGCAATGGCCTG	3993
rs193200785	snp	C/T	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75546416	GAGCCACTCCATCCA[C/T]AGAGTTGGTGTGAGG	3993
rs193202006	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75572613	GAGCTTGCAGTGAGC[C/T]GAGATTGTGCCACTG	3993
rs193237540	snp	C/G	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75561733	CGAGACCAGCTTGGG[C/G]AACATGGCGAAACCC	3993
rs193241835	snp	G/T	0.0248432	0.108648	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525615	CTGCGGCGCCGAGCT[G/T]GGGGGCGGGCCGGGG	3993
rs199497556	snp	A/T	8.24124e-05	0.00641868	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523640	AAGAGTTCATGTCAT[A/T]ACGTTTCTCATTGTA	3993
rs199621552	in-del	-/C	0.0517044	0.152246	intron-variant	LLGL2	GRCh38.p7	17:75550830	CAAACTAGGGGGCAA[-/C]TGGGGCACAGCCAGA	3993
rs199645090	snp	C/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523240	TGAGAAATGTGACTC[C/T]CCTCCCCAGTACCTT	3993
rs199656267	snp	C/T	8.38891e-05	0.00647592	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568534	GCTGGTGGTGATTGA[C/T]CTGCAGACAGCAGGC	3993
rs199685129	snp	A/C/G	0.000288031	0.0119978	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571703	TGTGGGCTGGCACCA[A/C/G]TGGGGGCACCATCTA	3993
rs199785141	snp	A/G	0.00318921	0.039805	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573625	AGAAGGCCCCGAGCC[A/G]AGCCAGGTGAGTGAA	3993
rs199816974	in-del	-/A	0.0263992	0.111815	intron-variant	LLGL2	GRCh38.p7	17:75561171	CTCTTGATGACACTT[-/A]ATCTAAGTTTTTAAA	3993
rs199832141	snp	C/T	0.00011765	0.00766884	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564387	CAGGGTGGCATGCCA[C/T]GGGCCAGCTACGGGG	3993
rs199860735	snp	C/T	0.000335965	0.0129565	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574640	TTCACATCGAGCCGC[C/T]GTGGGGTGCAGCCTC	3993
rs199913582	snp	C/G/T	7.21415e-05	0.00600552	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568825	CCCACCCCAGAGGGA[C/G/T]CTGCTGCTCACAGGG	3993
rs199921029	in-del	-/TATA			intron-variant	LLGL2	GRCh38.p7	17:75532049	TAAATTATATATATG[-/TATA]TATACACACACACAC	3993
rs199945561	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574309	AGGGGTGGGGAAGGG[G/T]GGTCAGGGTCAAGGG	3993
rs199973131	snp	A/G	0.000103045	0.00717718	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570449	TCCGCCGGATGCGTC[A/G]GAGCCGGGTGTCCAG	3993
rs199993387	snp	C/T	0.00299554	0.038585	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558621	TCACACTGCGTGGAC[C/T]CCCAGGGTAAGGGCT	3993
rs200040120	snp	A/C	0.00527782	0.0510985	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570200	CTCGTGGCCTTCGGC[A/C]CCAGCCATGGCTTTG	3993
rs200046748	snp	C/G/T	0.0402447	0.136031	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573619	GCCCCAAGAAGGCCC[C/G/T]GAGCCGAGCCAGGTG	3993
rs200100321	in-del	-/AAAA			intron-variant	LLGL2	GRCh38.p7	17:75527168	GTGAGACCCTGTCTC[-/AAAA]AAAAAAAAAAAAAGT	3993
rs200162738	snp	A/G	1.6528e-05	0.00287467	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524446	GATGGAGCTTGCTCC[A/G]GGGGACCGGGACTGT	3993
rs200220698	snp	A/G/T	0.000139258	0.00834341	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573597	CACCGCCCTGGTAAC[A/G/T]GTGCGGGCCCCAAGA	3993
rs200223371	snp	A/G	0.000495679	0.0157351	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563771	CTTTCCTTGCAAAGC[A/G]ATTACCAGAATCCTC	3993
rs200228117	snp	A/G	0.00161322	0.028355	missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523335	CTGATGGAGGTGCCC[A/G]GTAAGTTTCCAAGCA	3993
rs200230414	snp	A/G	0.00199806	0.0315442	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523789	TAGTGGGTACGCAGT[A/G]AGCCAGCACTGCCCC	3993
rs200239100	snp	A/G			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567950	CCTGTCTCGAGAAAA[A/G]AAAAAAAAAAAAAAA	3993
rs200275380	snp	A/G	0.00199792	0.0315431	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524354	CCCTGGTGGATCATG[A/G]TGACATCTCCTTCTA	3993
rs200277053	in-del	-/G	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75562196	CCTGGAGACGGGGCA[-/G]GGGTCAAGGCTCCAG	3993
rs200283598	snp	C/T	0.000242744	0.0110142	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559409	GACGCGGTGCTGCAG[C/T]GGTGAGCCCAGAGCC	3993
rs200304886	snp	C/T	0.000475398	0.0154102	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574243	TGGTGATGGAGCGCG[C/T]TCTGCTCAGTGATGA	3993
rs200319961	snp	A/G	0.00179489	0.0299035	intron-variant	LLGL2	GRCh38.p7	17:75571811	CAGGGAGAGCAGAGG[A/G]TGCTCGGGCTGCCTG	3993
rs200407635	snp	G/T	0.000188164	0.00969777	intron-variant	LLGL2	GRCh38.p7	17:75569347	GGCTGGGCTGGGGAG[G/T]GGGAGCTGGGGAGGA	3993
rs200429656	snp	C/T	4.96668e-05	0.00498307	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574946	TCGGGGGTCCCTGCC[C/T]CAACCGGAGAGGCCG	3993
rs200432063	snp	C/T	3.35587e-05	0.00409613	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570166	GGTCACCTCCTTGGC[C/T]CTGCACTCTGAGTGG	3993
rs200445428	snp	C/G	1.64833e-05	0.00287078	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524409	CCAGGATGTGGGGCA[C/G]TGACCTCACAGCTCT	3993
rs200453790	in-del	-/TG			intron-variant	LLGL2	GRCh38.p7	17:75548820	TCTCCTACAGTGGTA[-/TG]TTTTGGGGTGGTATG	3993
rs200484278	snp	A/G	0.000117207	0.00765439	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571036	GATCGAGGCTCGCTC[A/G]GCAGAGGACTCCTTC	3993
rs200564985	snp	G/T	0.000823574	0.0202758	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524233	AGTGGGCTATGGCTG[G/T]GTCTCACTCTAACCC	3993
rs200597703	snp	C/G	0.000798403	0.0199641	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568795	AATTGATGGTGGCAC[C/G]AGCCTGACCCCAGCC	3993
rs200648094	snp	A/G	9.98137e-05	0.00706377	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568676	GGCAGCCGGCAGAAC[A/G]CACACTTCTCCACCA	3993
rs200650788	snp	A/C/G	0.000429934	0.0146564	intron-variant	LLGL2	GRCh38.p7	17:75558122	CAGGGGATGGTGTCC[A/C/G]ACCTTCCAGAGCTTT	3993
rs200701234	snp	C/T	6.58968e-05	0.00573969	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523334	CCTGATGGAGGTGCC[C/T]GGTAAGTTTCCAAGC	3993
rs200719954	snp	C/T	0.000157844	0.00888239	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569073	TGTTCCTCACCGACA[C/T]GGACCCCAACGAGAA	3993
rs200779141	snp	C/T	0.00199802	0.0315439	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559303	GCCACATTCCTCCTG[C/T]GAGCTGCTCTACCTG	3993
rs200799378	snp	A/C	0.000798403	0.0199641	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568556	ACAGCAGGCTGGCCA[A/C]CGGTCCAGCTGCCCT	3993
rs200844471	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573922	CAGGGAGCCCGGGGG[C/T]CCTGGTCCTCACTGT	3993
rs200874163	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75529149	CAATAGAGTGAGACT[G/T]TCTCAAAAAAAAAGA	3993
rs200883350	snp	A/G/T	0.000155007	0.00880233	intron-variant	LLGL2	GRCh38.p7	17:75563296	CCGCCTCGGTCCAGC[A/G/T]TGCTGCCCTCTGTCC	3993
rs200886953	snp	C/T	0.00265076	0.0363091	intron-variant	LLGL2	GRCh38.p7	17:75573695	CCCTCTCTGAGATAC[C/T]GAGGCTCCCACTGCT	3993
rs200954432	snp	A/G/T	7.0123e-05	0.00592092	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570961	GCAGGCACAGGAGGG[A/G/T]AGTGCCAAGGCTGAG	3993
rs200955265	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559326	TCTACCTGGGCACCG[A/G]GAGTGGCAACGTGTT	3993
rs200994414	snp	G/T	1.66291e-05	0.00288345	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569286	GATCTTCCTCTGCAA[G/T]TACAGCGGCTACCTG	3993
rs200996856	snp	A/G	4.96184e-05	0.00498063	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558212	GAACAACGCTGTGAC[A/G]CAGATCCACCTCCTG	3993
rs201009590	snp	A/G	0.00199791	0.0315431	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563081	TGCAGGAGCACCCTC[A/G]AGACCCCAACCAGAT	3993
rs201034531	snp	C/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574313	GTGGGGAAGGGGGGT[C/G]AGGGTCAAGGGAGGC	3993
rs201137001	snp	A/G	0.0011207	0.0236452	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570473	TGTCCAGCCGGAAGC[A/G]GCACCCGGCTGGCCC	3993
rs201164163	snp	A/C/T	0.00124963	0.0249661	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558620	TTCACACTGCGTGGA[A/C/T]CCCCAGGGTAAGGGC	3993
rs201181868	in-del	-/G	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75554864	ACTGCACTCCAGCCT[-/G]GGCGACAGCGCAAGA	3993
rs201213445	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571764	GCGGAGAATGGATGA[A/G]CCTGTGCGGGCAGAG	3993
rs201231487	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75560846	AACAAAGAAAAAACA[-/T]TTTTTTTGAGAGAGT	3993
rs201240037	snp	A/G	6.67245e-05	0.00577562	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568658	GAGCGGATCATTGCC[A/G]CCGGCAGCCGGCAGA	3993
rs201265723	snp	A/G/T	6.81006e-05	0.00583492	intron-variant	LLGL2	GRCh38.p7	17:75563479	GTCAGTGTTTCACCC[A/G/T]CCGGGCAGGGCCCAC	3993
rs201300652	snp	C/T	0.000105132	0.00724949	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568997	GAGGACGGCACGGTG[C/T]GGTTCTGGGATGCCT	3993
rs201318934	snp	G/T	1.70269e-05	0.00291773	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568490	GCCTTTGACGACCCC[G/T]ATGCCCTGGTGGTGC	3993
rs201366813	snp	C/G	1.66161e-05	0.00288232	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543450	GTTCCTGAGGCCAGG[C/G]CATGACCCTGTGCGG	3993
rs201386309	snp	C/T	0.000325157	0.0127465	intron-variant	LLGL2	GRCh38.p7	17:75573646	GGTGAGTGAAAGGGC[C/T]AGAGGCCTCTCCCGC	3993
rs201392252	snp	C/T	0.00199798	0.0315436	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543433	CTAAGCAAAATGAGG[C/T]GGTTCCTGAGGCCAG	3993
rs201415896	snp	C/T	1.64754e-05	0.00287009	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524358	GGTGGATCATGGTGA[C/T]ATCTCCTTCTACAGC	3993
rs201458140	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549237	GGACAGGGCCACTGA[A/G]GACCAAGGGAAGGAA	3993
rs201480495	snp	A/G	0.000301948	0.0122834	intron-variant	LLGL2	GRCh38.p7	17:75556188	GCAGGGCCTTGGGGT[A/G]GGTGAGATTTGGGGA	3993
rs201503399	snp	C/T	0.000324995	0.0127433	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571672	TTCTCGGCAGGCTCC[C/T]GGCACTGCCCCTCGC	3993
rs201510982	snp	A/G	3.37092e-05	0.0041053	synonymous-codon, intron-variant	LLGL2	GRCh38.p7	17:75564521	CAGTAGGAGAGCTTC[A/G]GGAGTGGGTGCCCAG	3993
rs201553761	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75539625	TTTTTTTTTTTTTTT[-/A]TATACAGAATTTCAC	3993
rs201555254	snp	A/C	5.46155e-05	0.00522539	intron-variant	LLGL2	GRCh38.p7	17:75573288	GCCAAGGTGTTTGAG[A/C]CGGGCTGGGTGGGTG	3993
rs201602163	snp	A/G	0.00199803	0.031544	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568777	CTTTTTCTAGGAGTG[A/G]CCAATTGATGGTGGC	3993
rs201620727	snp	A/G	0.00791508	0.0624091	intron-variant	LLGL2	GRCh38.p7	17:75573444	GCAGCCTTGGCAGCC[A/G]CCAGGCCAGGCCGCT	3993
rs201628762	in-del	-/TC			intron-variant	LLGL2	GRCh38.p7	17:75530648	GAGCGAGACTCCATT[-/TC]AAAAAAAAAAAAAAA	3993
rs201650903	snp	A/C/T	6.68554e-05	0.00578134	intron-variant	LLGL2	GRCh38.p7	17:75556170	CCCCTCGCTCCCACT[A/C/T]GGGCAGGGCCTTGGG	3993
rs201683909	snp	A/G	0.000118798	0.00770616	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559304	CCACATTCCTCCTGC[A/G]AGCTGCTCTACCTGG	3993
rs201741398	snp	A/G	0.000520121	0.016118	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563111	TCCTGATCGGCTACA[A/G]CCGAGGCCTCGTTGT	3993
rs201752938	snp	C/T	2.30816e-05	0.0033971	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570091	AGCCCGCTCAGGGCC[C/T]GTGCGCTTTGAGCCT	3993
rs201775186	snp	C/T	3.31961e-05	0.00407394	upstream-variant-2KB, stop-gained, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523733	GCTGTGGCCACATTC[C/T]GAAAGAATAACCCTG	3993
rs201813210	snp	A/G	3.51537e-05	0.00419233	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569029	GGGTGTCTGCCTGCG[A/G]CTGCTCTACAAACTC	3993
rs201875861	snp	A/G	0.00199804	0.031544	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559339	CGAGAGTGGCAACGT[A/G]TTTGTGGTGCAGCTG	3993
rs201910049	snp	A/C/T	0.00129143	0.0253807	intron-variant	LLGL2	GRCh38.p7	17:75562987	CCTGGTGGACGGCAT[A/C/T]GGAGGCTCACGGCAC	3993
rs201926585	snp	C/T	0.000213728	0.0103353	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574529	CAGCTGGGGTGGGCC[C/T]GAGGCTCTGCCAGAG	3993
rs201959215	snp	A/G/T	0.000238351	0.0109141	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574240	GCCTGGTGATGGAGC[A/G/T]CGCTCTGCTCAGTGA	3993
rs202021846	snp	C/G			synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559309	TTCCTCCTGCGAGCT[C/G]CTCTACCTGGGCACC	3993
rs202033148	snp	A/G	0.000501839	0.0158325	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570020	GTGGAGCAGGTGGAG[A/G]CCGACCTGCTGCAGG	3993
rs202100751	snp	A/G	1.69786e-05	0.0029136	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573034	CACGCTGCCCAAGGT[A/G]AGTGCCAAGCTGAAG	3993
rs202109896	snp	C/G/T	9.12141e-05	0.00675276	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523783	GTGCATTAGTGGGTA[C/G/T]GCAGTGAGCCAGCAC	3993
rs202123899	snp	A/G	0.000194248	0.00985325	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574651	CCGCCGTGGGGTGCA[A/G]CCTCAGCAATGGCGG	3993
rs202146836	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75547839	CAAAAAAAAAAAAAA[A/T]GAGGACTGGGGTGGA	3993
rs202158524	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529198	CCTGCCTGACAGTCC[C/T]TTTCTTTTTTTTTCT	3993
rs202192830	snp	C/T	0.000589657	0.0171604	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543411	GGTCTCCAGTGGGGG[C/T]TGCAGACTAAGCAAA	3993
rs202211646	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537356	AACCCATCTTGACCA[C/T]TCTCAGGACTCTGAG	3993
rs367585751	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531078	TGGGTACACCCTCCT[C/T]ACCCTGCTGGGTGGC	3993
rs367602498	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571078	CCGGACCCTGTACTT[C/T]GCTGACACCTACCTG	3993
rs367604966	snp	C/T	0.000188285	0.00970088	intron-variant	LLGL2	GRCh38.p7	17:75568864	TTTGATGCTACCCCA[C/T]CTCTTCCCAGTAGGA	3993
rs367612817	snp	A/C/T	8.33791e-05	0.00645627	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559336	CACCGAGAGTGGCAA[A/C/T]GTGTTTGTGGTGCAG	3993
rs367615652	snp	A/G	4.96767e-05	0.00498356	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574943	CTTTCGGGGGTCCCT[A/G]CCCCAACCGGAGAGG	3993
rs367641476	snp	G/T	0.000193981	0.00984647	intron-variant	LLGL2	GRCh38.p7	17:75574819	AGCGTGGGCGGCTGG[G/T]GCACCCCGTCCTGCC	3993
rs367658427	snp	A/C/G	3.66651e-05	0.00428153	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523786	CATTAGTGGGTACGC[A/C/G]GTGAGCCAGCACTGC	3993
rs367674317	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75547550	TGACGAGAGGCGGGG[C/T]GCAGTGGCTCATGCC	3993
rs367677773	snp	A/G	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75562912	TTTCTATGCTGGCAC[A/G]TGGAGCAGCCACCTC	3993
rs367706425	snp	C/G/T	6.8254e-05	0.00584149	intron-variant	LLGL2	GRCh38.p7	17:75571799	GTGAGTGCTGGGCAG[C/G/T]GAGAGCAGAGGGTGC	3993
rs367748605	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527126	GTGAGTCATGATGGC[A/G]CCACCACACTCCAGC	3993
rs367823640	snp	A/G	0.000218922	0.0104601	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523784	TGCATTAGTGGGTAC[A/G]CAGTGAGCCAGCACT	3993
rs367836297	snp	A/G	0.000153988	0.00877327	intron-variant	LLGL2	GRCh38.p7	17:75570304	GTGGGGCCCGCGAGG[A/G]CTCCCAGGACCTAGC	3993
rs367836428	snp	A/G	3.53145e-05	0.0042019	intron-variant	LLGL2	GRCh38.p7	17:75562988	CTGGTGGACGGCATC[A/G]GAGGCTCACGGCACT	3993
rs367857717	multinucleotide-polymorphism	GTC/TTT			intron-variant	LLGL2	GRCh38.p7	17:75547108	TTTTTGTCCAACACC[GTC/TTT]TGGCTCAACTCCTTT	3993
rs367870566	snp	A/C/G/T	5.47154e-05	0.00523022	intron-variant	LLGL2	GRCh38.p7	17:75573289	CCAAGGTGTTTGAGC[A/C/G/T]GGGCTGGGTGGGTGT	3993
rs367897479	snp	G/T	6.71377e-05	0.00579348	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568531	GGAGCTGGTGGTGAT[G/T]GACCTGCAGACAGCA	3993
rs367902399	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549124	CACCTCCCTTCACAC[C/T]TCAGTTACTTCACCA	3993
rs368103155	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575026	AGCTGCTCTGGGCCT[C/T]GGGAGAGGAGAGACC	3993
rs368135139	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75527538	ATGACACTACATTCA[A/T]AAATAAGAAATAAAA	3993
rs368206184	snp	G/T	1.66468e-05	0.00288498	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568607	TCCGCCATCACCTGC[G/T]CTCACCACGTCTCCA	3993
rs368213101	snp	A/G	1.68295e-05	0.00290077	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523753	GAATAACCCTGGCAA[A/G]CCCTATGCCCGGATG	3993
rs368284545	snp	A/G	3.41559e-05	0.00413241	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572004	GGCCCATGATCTGTC[A/G]AAGAGCCCTGACATG	3993
rs368291164	snp	C/T	0.000165224	0.0090876	intron-variant	LLGL2	GRCh38.p7	17:75574826	GCGGCTGGGGCACCC[C/T]GTCCTGCCCAGGGTG	3993
rs368318098	snp	A/C/G	0.000104117	0.00721448	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559410	ACGCGGTGCTGCAGC[A/C/G]GTGAGCCCAGAGCCC	3993
rs368337169	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530606	AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG	3993
rs368347662	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75544132	CAGGAGTCTGGGGCC[C/T]GAGAAGGTCAGGACG	3993
rs368354171	in-del	-/CGCCGAGGGA	0.48155	0.0942576	utr-variant-5-prime, intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75525777	GGGGCCGGCGGCGGG[-/CGCCGAGGGA]CGCCGAGGGACGCCG	3993
rs368377423	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75572780	AGCCGAGATCACACC[A/T]CTGTACTCCAGCCTG	3993
rs368384635	snp	A/C/G	0.000363648	0.0134801	intron-variant	LLGL2	GRCh38.p7	17:75571621	TGCCCAGCTCCACCC[A/C/G]ACTCCCACGCTAAGG	3993
rs368385489	snp	A/G	0.000198756	0.00996686	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570188	TCTGAGTGGCGGCTC[A/G]TGGCCTTCGGCACCA	3993
rs368386613	snp	A/G	3.7165e-05	0.00431059	intron-variant	LLGL2	GRCh38.p7	17:75573307	GCTGGGTGGGTGTCG[A/G]GGCCCCGGGCACTGC	3993
rs368393996	snp	A/G	0.000206188	0.0101514	intron-variant	LLGL2	GRCh38.p7	17:75559231	CAGTGGTCGGCTCAC[A/G]GGCAGCTGTTCTTGT	3993
rs368451610	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75550048	TGTGGGCGGGGCCGG[A/G]TAGGCTGGATGCCGC	3993
rs368508877	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75537228	GATTTTTTCTGACAG[C/G]TTAATAAACAGCACA	3993
rs368527901	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75549460	CCGTGCCCACCCTCC[-/T]CTGTCCCCTTAGGCC	3993
rs368567805	snp	A/G	0.000134021	0.00818491	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556048	CTTCTCGTTGCAGAC[A/G]GTGGAGCATGGCTTC	3993
rs368596814	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75572935	GGAGGCATGTGGGGA[C/G]GGGAGGGCCCAGCAG	3993
rs368604286	snp	A/G	5.25537e-05	0.00512582	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569014	GTTCTGGGATGCCTC[A/G]GGTGTCTGCCTGCGG	3993
rs368880235	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75561189	CTAAGTTTTTAAAAC[A/G]TGCAACCCTTTAGTC	3993
rs368925383	snp	C/G	1.69516e-05	0.00291127	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573530	CTTCTCTCTCTCCAC[C/G]AAGTGGCTGGTGGAG	3993
rs368962083	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75552112	CCAATTAGGTGACAG[A/T]GGGAGACTCTGTCTT	3993
rs368997071	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528441	TTTAATATACCGCAA[C/T]ATTAAAAGAAAAAAA	3993
rs369025981	snp	A/G/T	0.000116087	0.0076179	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558227	GCAGATCCACCTCCT[A/G/T]CCCGGCCAGGTGAGG	3993
rs369039224	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75528759	AAACAAACAAACAAA[A/C]AATGGCCCATAATCC	3993
rs369106141	snp	A/C	0.000875616	0.0209055	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543371	AGTGCCAGGACAGAC[A/C]CCTGCAGCTCCTTCT	3993
rs369146215	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542297	TGTTCCCTCTCCCTC[C/T]TGCAGTCAAAGCACT	3993
rs369159097	snp	A/G	3.29478e-05	0.00405867	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523328	CACCTTCCTGATGGA[A/G]GTGCCCGGTAAGTTT	3993
rs369177929	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532625	GGGGGGGTTTCCACC[A/G]TGTTGGTCAGGCTGG	3993
rs369181970	snp	C/T	1.89446e-05	0.00307765	intron-variant	LLGL2	GRCh38.p7	17:75572077	AAGGTGCCACACGGG[C/T]AGCGGCGGGTCTCCC	3993
rs369262132	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552421	TTGAACCAGGGAGGC[A/G]GAGGTTGCAGTGAGC	3993
rs369269336	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75571519	TGAGCTGACCTGGGA[C/T]TGGGGTCTTCTATGT	3993
rs369323008	snp	C/T	0.000408922	0.0142931	intron-variant	LLGL2	GRCh38.p7	17:75573005	TGAACAACCACCCCA[C/T]GCCCCCAGGTGTTCA	3993
rs369379812	snp	A/G	1.93142e-05	0.00310752	intron-variant	LLGL2	GRCh38.p7	17:75569918	TCCTGCGGCCCTGCC[A/G]TCCCTTTGCTGAGGG	3993
rs369437156	in-del	-/C	0.050951	0.15126	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525192	GGCGCCCCCCCGCAC[-/C]CCCCCCCCGAGGAAA	3993
rs369448132	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75543622	CTGCCTGCAGTGCCT[C/G]TTGGGACTCAGACTT	3993
rs369484057	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75572825	ACTCCATCTCGGAGG[-/A]AAAAAAAAAAAATCC	3993
rs369539079	snp	C/T	0.000175985	0.00937878	intron-variant	LLGL2	GRCh38.p7	17:75573654	AAAGGGCCAGAGGCC[C/T]CTCCCGCCCCTCCCG	3993
rs369557572	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75555715	CCACACCCATAAGGC[C/T]CCCATGCCACTGAGG	3993
rs369562119	snp	A/G	0.00011263	0.00750347	intron-variant	LLGL2	GRCh38.p7	17:75573329	GGGCACTGCACGGAC[A/G]GGAAGGGTGGCCAGG	3993
rs369564274	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531835	TTTGAATACTCACCC[C/T]TCTCTTCTTCCCAGG	3993
rs369566488	snp	A/G	0.000103386	0.00718904	intron-variant	LLGL2	GRCh38.p7	17:75573904	AGGGCTCTCAGAGCC[A/G]GGCAGGGAGCCCGGG	3993
rs369587197	snp	A/T	0.000153988	0.00877328	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574576	GAGAGTGGAGGTCCC[A/T]GAGGCCATGACTCCC	3993
rs369689230	snp	A/G	0.000135142	0.00821905	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573107	AGCGTGGCCCACTTC[A/G]GCAGTCGTCGAGCCG	3993
rs369765488	snp	C/T	2.5381e-05	0.00356228	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570419	AGTCCCTCAAGAAGT[C/T]CTTGCGTCAGTCATT	3993
rs369789793	snp	C/T	3.2962e-05	0.00405954	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523617	GATGGAAAAGAAAGG[C/T]TGGGGAGAAGAGTTC	3993
rs369863506	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75536565	CGCCTGGTGAGCACC[A/G]GAACATTCCACCAGC	3993
rs369887246	snp	A/G	1.67279e-05	0.002892	intron-variant	LLGL2	GRCh38.p7	17:75569176	GGCAGAGGCCAGCTG[A/G]GTCCTGTCCCCGTGG	3993
rs369946119	snp	C/T	1.78245e-05	0.00298529	intron-variant	LLGL2	GRCh38.p7	17:75571862	TCCAGCCCTGCCACC[C/T]CCTCACCAGCCCCAA	3993
rs370078960	snp	A/G	0.000437904	0.0147905	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574961	CCAACCGGAGAGGCC[A/G]GTGCACAGGGCCCCG	3993
rs370101388	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572131	AGGCTCGGACCTTGG[A/G]CAAAAATGATGGCTG	3993
rs370162566	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75554867	GCACTCCAGCCTGGG[C/T]GACAGCGCAAGACTC	3993
rs370197059	snp	A/G	0.0115144	0.0749975	intron-variant	LLGL2	GRCh38.p7	17:75531219	GGACTTCCTGGCCCC[A/G]GGACCCTCCCTTTGG	3993
rs370254590	snp	A/G	0.000219864	0.0104825	intron-variant	LLGL2	GRCh38.p7	17:75568729	AGCCCCAGCCCCACC[A/G]CAAGCCAAACTCTCC	3993
rs370262429	snp	A/G	0.000106781	0.00730608	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569995	GAATGACGAGGCAGC[A/G]GAGCAGGCTGTGGAG	3993
rs370269067	snp	C/G	1.74659e-05	0.0029551	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573255	GTGGCATCGCCTCCT[C/G]CGTCTTCACCAAATA	3993
rs370274464	snp	A/G	0.000202327	0.010056	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573979	TCAGAGTGATGGCGA[A/G]GGTAAGACAGGCCTC	3993
rs370275407	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75526811	TGACAAGGAAACGCT[A/G]GTAGGAAGAGCAGAG	3993
rs370299150	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532377	TGACTCAGGCTCCCG[A/G]GTAGCTGGGATTACA	3993
rs370324649	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75565383	TGAGGGGGCGGGGCT[C/G]TTCAGGACACCTGGT	3993
rs370375483	snp	C/G	3.42489e-05	0.00413803	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571924	CAGCTGATGCACCGG[C/G]CGCCGGTGGTGGGCA	3993
rs370443752	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75544684	ACCTCCCTGTTGGGA[C/G]AGGTGGGTCGTGGGG	3993
rs370466207	snp	C/T	5.05813e-05	0.00502872	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573209	CTCAAGCCCCAGGTG[C/T]GCTACAGCTGCATCC	3993
rs370520316	snp	C/T	1.78134e-05	0.00298436	intron-variant	LLGL2	GRCh38.p7	17:75571863	CCAGCCCTGCCACCC[C/T]CTCACCAGCCCCAAC	3993
rs370584981	snp	A/G	5.02769e-05	0.00501358	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568547	GACCTGCAGACAGCA[A/G]GCTGGCCACCGGTCC	3993
rs370595794	snp	C/T	0.000251007	0.0112	intron-variant	LLGL2	GRCh38.p7	17:75570267	TTAAGTGAGCAGGGG[C/T]GGCTGGGTCCCGGGG	3993
rs370601184	snp	A/C/G	3.31164e-05	0.00406904	intron-variant	LLGL2	GRCh38.p7	17:75563708	GGGACTGACACTTGT[A/C/G]TGAGAGTTTGAGGAT	3993
rs370676948	snp	A/G	1.82964e-05	0.00302455	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574700	TGAGTGCAGCTGCCA[A/G]CCGTGCTGGGAAGGG	3993
rs370708679	snp	C/G/T	0.000593042	0.0172096	upstream-variant-2KB, missense, stop-gained, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524395	GACTTCACGTTGCCC[C/G/T]AGGATGTGGGGCACT	3993
rs370744823	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549952	TTCTGCAAATCTTTG[C/T]TCTCCTTTCCCAACC	3993
rs370768544	snp	A/G	0.000113707	0.00753928	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558575	CTGAAGGTCAAGGGC[A/G]GGGCATCGGAGCTGC	3993
rs370788459	snp	C/T	0.000118627	0.00770061	synonymous-codon, intron-variant	LLGL2	GRCh38.p7	17:75564530	AGCTTCGGGAGTGGG[C/T]GCCCAGGGTTAGGTG	3993
rs370861025	snp	A/G	0.000108605	0.00736823	intron-variant	LLGL2	GRCh38.p7	17:75568970	TGGCAGGTGGGTTCT[A/G]CCCACAGGCACGAGG	3993
rs370870539	snp	C/T	7.59244e-05	0.00616088	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570064	CCGCTGGAAGGGGCA[C/T]GAGCGCCTGGCAGCC	3993
rs370885909	snp	C/G	1.65864e-05	0.00287974	intron-variant	LLGL2	GRCh38.p7	17:75563848	CTCTCCAGAGCCTTC[C/G]TGGAGGGCTAGAAAG	3993
rs370908986	snp	C/T	0.000225887	0.0106251	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574403	GTGGAAGGGCTGTGG[C/T]TAGCCGCCCCAAGGG	3993
rs370929840	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75540512	CCTGCCCAGCCAGAC[C/G]TCGCCAGCACCCTGT	3993
rs370951923	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558958	CCCGCCTCCTCCATC[C/T]GCACCCCGCCTCCTC	3993
rs370964495	snp	A/C/G	0.000268054	0.011574	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571065	TCACAGGCTTCGTCC[A/C/G]GACCCTGTACTTTGC	3993
rs371012842	snp	C/T	4.98434e-05	0.00499192	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556135	CACCCGTTCTGGAGC[C/T]ATCAAGCTGTATCCT	3993
rs371123285	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537317	TGGATCATTTTATCC[C/T]AAGGTGTGTTTCTTC	3993
rs371125810	snp	C/T	0.000135249	0.00822231	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571743	CCTGCGTGTGCCTCC[C/T]GCCGAGCGGAGAATG	3993
rs371130689	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75553291	TGCAGGGCAGGCCCT[A/G]TTCCTAGCAAAGGCC	3993
rs371135404	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75561905	CCAGCCTGGGCAACA[C/G]AGCGAGACTCCCATC	3993
rs371140105	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529637	GGAGACCGAGGCAGA[C/T]GGATCATGAGGTCAG	3993
rs371170583	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75546199	GCCAGGCCTTGGGAG[G/T]GGGAGCCCAGGCCAG	3993
rs371172844	snp	A/G	8.81251e-05	0.00663738	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574506	CGCGGGTGAGGCACC[A/G]CCCAGGCCAGCTGGG	3993
rs371194140	snp	A/G	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75563225	TGTTGCTCTCCCAGG[A/G]CCCCAAGTGGCACAT	3993
rs371197955	snp	A/G	1.82998e-05	0.00302482	intron-variant	LLGL2	GRCh38.p7	17:75570929	CCAGAGCTGACCCTT[A/G]GGCTGGCCCACCCCT	3993
rs371201693	snp	A/G	0.00103352	0.0227088	intron-variant	LLGL2	GRCh38.p7	17:75562998	GCATCGGAGGCTCAC[A/G]GCACTCCCCTCGCCC	3993
rs371209437	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555758	GTCACCCAGGGTGCA[C/T]GTGGTGGAGGCACCG	3993
rs371263513	snp	C/T	0.000638465	0.0178557	intron-variant	LLGL2	GRCh38.p7	17:75568933	AGCCCCTGGGCATCC[C/T]GGCTGGCATCCCTCT	3993
rs371270086	snp	C/T	1.71749e-05	0.00293038	intron-variant	LLGL2	GRCh38.p7	17:75563226	GTTGCTCTCCCAGGG[C/T]CCCAAGTGGCACATA	3993
rs371276273	snp	A/G	2.87237e-05	0.00378959	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570122	GGCTTTCAGCCCTTC[A/G]TGTTGGTGCAGTGTC	3993
rs371305346	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75541391	CCCCCAGGCTGCAAT[G/T]CTGGGCCAGCAGATC	3993
rs371311148	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555034	TACAAAAAATTAGCC[A/G]GGCATGGTGGTGGGC	3993
rs371363686	snp	C/T	9.88338e-05	0.00702902	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523239	CTGAGAAATGTGACT[C/T]CCCTCCCCAGTACCT	3993
rs371384731	snp	A/G	0.000461893	0.0151899	intron-variant	LLGL2	GRCh38.p7	17:75558497	CCACATGATCCCGTC[A/G]TGTGCCCTCGCCAGT	3993
rs371398841	in-del	-/CC			frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564403	GGCCAGCTACGGGGA[-/CC]CCGCCACTGCATCTC	3993
rs371502131	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569074	GTTCCTCACCGACAC[A/G]GACCCCAACGAGAAC	3993
rs371517081	snp	C/T			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573060	TGAAGTTGAAGCTGA[C/T]GGCCCTGGAGGGCTC	3993
rs371526333	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75562956	CCATGGCTGTGCCAT[C/G]CTGGGGGCCATTCCC	3993
rs371550554	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75537636	CTGGGAAACACAGTT[A/G]CAGTGAGCTAAGATT	3993
rs371565109	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75532266	TAATTTTTTGTTTGT[A/T]TTGAGACGGAGACTT	3993
rs371570709	snp	A/C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555941	GAACCGGAAAGGTAC[A/C/T]GAAGCCCTGCTTCCT	3993
rs371579928	snp	A/G	3.53776e-05	0.00420565	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574641	TCACATCGAGCCGCC[A/G]TGGGGTGCAGCCTCA	3993
rs371603055	snp	C/T	0.0178098	0.0926698	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543321	GAGAGAGAGGCCCTG[C/T]TCCACCTGTTTGGGC	3993
rs371634207	in-del	-/AAGAG			intron-variant	LLGL2	GRCh38.p7	17:75535325	TGGGGAGCACGAGCG[-/AAGAG]GAGAGGAGAGCATGG	3993
rs371650108	snp	C/T	3.43743e-05	0.0041456	intron-variant	LLGL2	GRCh38.p7	17:75573456	GCCGCCAGGCCAGGC[C/T]GCTAGCATTGCCCCC	3993
rs371650238	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560066	GAGGCCAGGGTGCTG[A/G]GCCCCTGGCCCTGCA	3993
rs371652084	snp	A/G	0.000680187	0.0184291	intron-variant	LLGL2	GRCh38.p7	17:75558102	GGCCTGGCACTCAAG[A/G]CAGGCAGGGGATGGT	3993
rs371719084	in-del	-/G	0.000150766	0.00868103	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573619	CCCCAAGAAGGCCCC[-/G]GAGCCGAGCCAGGTG	3993
rs371727851	snp	A/G	3.34482e-05	0.00408937	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559369	GCCAGCTTTTCGTGC[A/G]CTGGAGGACCGGACC	3993
rs371740230	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549231	GCACCAGGACAGGGC[C/T]ACTGAGGACCAAGGG	3993
rs371761340	snp	A/G	0.000135277	0.00822314	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563050	CACCGGCGTGTGTTC[A/G]AGATGGTGGAGGCAC	3993
rs371807271	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75535294	GGAAGGCAGCTTCTT[A/G]ATCAGCAGCGGGCTG	3993
rs371822270	snp	A/G	0.00281643	0.0374204	intron-variant	LLGL2	GRCh38.p7	17:75557987	CCCAGGGCCAGGGCT[A/G]CTGTGTCTCCTCCCC	3993
rs371950118	snp	C/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561724	TCAGGAGTTCGAGAC[C/G]AGCTTGGGCAACATG	3993
rs372002303	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536206	TCATCTCAGAGGTGG[C/T]GCTCTGGCTAGGTGG	3993
rs372111222	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560007	GATCATGTTGGGGCC[A/G]GGTCGGTCATGGTGG	3993
rs372142244	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572336	AGCCTGGCCAATATG[A/G]TGAAACCCTGACTAC	3993
rs372160474	snp	A/G	8.93807e-05	0.00668449	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559280	GCCACACAGATCACC[A/G]TGGTCCTGCCACATT	3993
rs372195190	snp	A/T			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564957	CAAGGTGCAGTGTCA[A/T]CAAGCCCTACAGCTC	3993
rs372236976	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75539907	AGTTACTGCGGCTGG[C/T]TGGAAATCATCCCAT	3993
rs372252800	snp	A/G	0.000193981	0.00984646	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574558	AGGGCTCAGGGGAGC[A/G]CTGAGAGTGGAGGTC	3993
rs372261133	snp	C/T	0.000447119	0.0149452	intron-variant	LLGL2	GRCh38.p7	17:75573313	TGGGTGTCGGGGCCC[C/T]GGGCACTGCACGGAC	3993
rs372314047	snp	A/G	7.58294e-05	0.00615702	intron-variant	LLGL2	GRCh38.p7	17:75572074	TTCAAGGTGCCACAC[A/G]GGCAGCGGCGGGTCT	3993
rs372319353	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75561211	CTTTAGTCTCATAAC[-/CT]TGTCTCTGAGAAGTC	3993
rs372327675	snp	A/G/T	3.34299e-05	0.00408828	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556066	GGAGCATGGCTTCCC[A/G/T]CACCAGCCCAGCGCC	3993
rs372348546	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75570790	GCAGGCTCCCCCAAG[C/G]GCACCTCCCTCTTGG	3993
rs372348868	snp	C/G	0.000258618	0.0113685	intron-variant	LLGL2	GRCh38.p7	17:75563285	CGATGGGAACGCCGC[C/G]TCGGTCCAGCGTGCT	3993
rs372349081	snp	C/T	0.000261322	0.0114277	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573596	CCACCGCCCTGGTAA[C/T]GGTGCGGGCCCCAAG	3993
rs372371252	in-del	-/CTC	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75560594	TGGGTTCAAGCTATT[-/CTC]CTGCCTCAGCCTCCC	3993
rs372378903	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575065	CTGGGCTGCCCTTCC[C/T]GGGCCTCGTCTGTCT	3993
rs372442669	snp	A/G	0.000155988	0.00883005	intron-variant	LLGL2	GRCh38.p7	17:75571139	GGGGCAGGGGGTAGT[A/G]GGCAGCAGACACCCC	3993
rs372542628	snp	C/T	3.37314e-05	0.00410665	intron-variant	LLGL2	GRCh38.p7	17:75558275	GAAGCCACTTCCATG[C/T]CCTCCTTGCCTTCAC	3993
rs372576504	snp	C/T	0.000115608	0.00760201	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558158	GCCTACTCCTAGCTA[C/T]GGAGCCCCAGGCGTG	3993
rs372592408	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558878	CCCGCCTCCTCCATC[C/T]GCACCCCACCTCCTC	3993
rs372600949	snp	A/G	3.30469e-05	0.00406477	intron-variant	LLGL2	GRCh38.p7	17:75574827	CGGCTGGGGCACCCC[A/G]TCCTGCCCAGGGTGA	3993
rs372629713	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532525	GCCTCCCGGGTTCAA[A/G]CAATTCTCCTGCCTC	3993
rs372634016	snp	A/G	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75568737	CCCCACCGCAAGCCA[A/G]ACTCTCCCATGGACT	3993
rs372768169	snp	C/T	5.72863e-05	0.00535162	intron-variant	LLGL2	GRCh38.p7	17:75572080	GTGCCACACGGGCAG[C/T]GGCGGGTCTCCCTGG	3993
rs372808279	snp	C/T	0.000708538	0.0188087	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573976	GACTCAGAGTGATGG[C/T]GAGGGTAAGACAGGC	3993
rs372830369	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75557296	CAGGGCTCGGCAGCT[C/G]TCTTCCAAATTCCAC	3993
rs372865631	snp	A/C/G	0.000419735	0.0144807	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574633	ACTGGCGTTCACATC[A/C/G]AGCCGCCGTGGGGTG	3993
rs372867184	snp	C/T	1.69527e-05	0.00291137	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573224	CGCTACAGCTGCATC[C/T]GCCGGGAGGACGTCA	3993
rs372869874	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564465	GACTTCACCTCCCGT[A/G]TCATCGGCTTCACTG	3993
rs372885842	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75525883	GGGGCTTCCACCTGG[A/G]GCGGGGAGGCCAGGG	3993
rs372916600	snp	C/T	0.000458158	0.0151284	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569042	CGGCTGCTCTACAAA[C/T]TCAGCACTGTGCGCG	3993
rs372927980	snp	C/T	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75574823	TGGGCGGCTGGGGCA[C/T]CCCGTCCTGCCCAGG	3993
rs372940306	in-del	-/AAAAAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75560803	GTTTGTTTATTTATT[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	3993
rs372977276	snp	C/T	0.000156296	0.00883877	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570439	CGTCAGTCATTCCGC[C/T]GGATGCGTCGGAGCC	3993
rs373111180	snp	C/T	0.000353419	0.0132885	intron-variant	LLGL2	GRCh38.p7	17:75570520	CCTGAGGTGAGGCTG[C/T]GGCCGGCCACGCACC	3993
rs373138654	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523879	CCAGCGTGCCAATCT[C/T]TGAGAGGAACAGGAG	3993
rs373166096	snp	A/G	8.36351e-05	0.00646611	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564399	CCACGGGCCAGCTAC[A/G]GGGACCGCCACTGCA	3993
rs373180529	snp	C/T	3.35272e-05	0.0040942	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563087	AGCACCCTCGAGACC[C/T]CAACCAGATCCTGAT	3993
rs373194328	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528802	GTTCATTTAAAAAAT[A/G]GAAAAGGCAATAGGA	3993
rs373242084	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560550	AGAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC	3993
rs373288922	snp	A/C	1.91679e-05	0.00309574	intron-variant	LLGL2	GRCh38.p7	17:75569943	TGAGGGCTTGCTGAG[A/C]CACCTGCCACCCTGC	3993
rs373341692	snp	A/G	5.08375e-05	0.00504145	missense, intron-variant	LLGL2	GRCh38.p7	17:75564531	GCTTCGGGAGTGGGT[A/G]CCCAGGGTTAGGTGT	3993
rs373439387	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75536312	CTCTTCTCCACATTC[C/T]TCCCAGGTGTGTCAC	3993
rs373532638	snp	C/T	1.73791e-05	0.00294775	intron-variant	LLGL2	GRCh38.p7	17:75543541	TGACCCCCAGGTTTT[C/T]GGCCAAGCAGCTCAG	3993
rs373565205	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75547894	AGGGGAGGAAGTGTA[A/G]GTGAATGAAGGTTGT	3993
rs373591655	snp	A/G	1.65877e-05	0.00287986	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569255	ACAGTGATGACCCCC[A/G]GCTGGGCATCCAGAA	3993
rs373611499	snp	A/G	6.61638e-05	0.00575131	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574933	TACTGATGGCCTTTC[A/G]GGGGTCCCTGCCCCA	3993
rs373653061	in-del	-/G	0.000466072	0.0152584	intron-variant	LLGL2	GRCh38.p7	17:75558020	CTAGGCTCCATGCAT[-/G]GGGTCCTGCTGCCTC	3993
rs373715661	snp	C/T	3.4525e-05	0.00415467	intron-variant	LLGL2	GRCh38.p7	17:75563287	ATGGGAACGCCGCCT[C/T]GGTCCAGCGTGCTGC	3993
rs373717414	snp	A/T	1.69026e-05	0.00290706	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571748	GTGTGCCTCCCGCCG[A/T]GCGGAGAATGGATGA	3993
rs373727654	snp	A/G	1.76487e-05	0.00297053	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569046	TGCTCTACAAACTCA[A/G]CACTGTGCGCGTGTT	3993
rs373729540	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555817	TGGTATGGTGTCGGG[A/G]AAGATCAGCTCGCAG	3993
rs373765888	snp	C/T	1.69327e-05	0.00290965	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573220	GGTGCGCTACAGCTG[C/T]ATCCGCCGGGAGGAC	3993
rs373774180	snp	A/G	1.66236e-05	0.00288297	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543444	GAGGCGGTTCCTGAG[A/G]CCAGGGCATGACCCT	3993
rs373790900	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75555392	CTCAGTTTTTGTTCT[C/T]AAACATCTTTATACC	3993
rs373811892	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75531627	TGTCAGGAGCAGTTT[G/T]CAGAGAGAAAACTGG	3993
rs373833716	snp	C/T	0.000875616	0.0209055	intron-variant	LLGL2	GRCh38.p7	17:75574815	GCTCAGCGTGGGCGG[C/T]TGGGGCACCCCGTCC	3993
rs373885102	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75532638	CCATGTTGGTCAGGC[G/T]GGTCTCTAACTCCTG	3993
rs373902704	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75563967	GGTAGACGCTATTCA[C/T]GTCTCTCAGCGGCCC	3993
rs373936735	snp	A/C	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574977	GTGCACAGGGCCCCG[A/C]CAGGGGCTGGGGGCA	3993
rs373938117	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573114	CCCACTTCGGCAGTC[A/G]TCGAGCCGAGGACTA	3993
rs373939600	snp	A/C			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574994	AGGGGCTGGGGGCAT[A/C]CCGGCTTCCACAATG	3993
rs373944403	snp	C/T	0.000226244	0.0106335	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574408	AGGGCTGTGGCTAGC[C/T]GCCCCAAGGGCCTCA	3993
rs373983943	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75556306	AAAATGGGGCAGGTA[C/T]GGTTGATGGTGGAGC	3993
rs373994073	snp	A/G	2.83226e-05	0.00376304	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558615	AGAGCTTCACACTGC[A/G]TGGACCCCCAGGGTA	3993
rs373997117	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532399	GGGATTACAGGCGCC[C/T]GCCACCACGCCCAGC	3993
rs374016404	snp	C/T	0.000150702	0.00867919	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568557	CAGCAGGCTGGCCAC[C/T]GGTCCAGCTGCCCTA	3993
rs374166709	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75543988	CTGCAGGCTGAACAC[C/G]TGATTCCTTCTGGCT	3993
rs374182771	snp	C/T	0.000153988	0.00877327	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570129	AGCCCTTCGTGTTGG[C/T]GCAGTGTCAGCCCCC	3993
rs374212529	snp	A/C	1.67705e-05	0.00289568	intron-variant	LLGL2	GRCh38.p7	17:75558266	GTGGGACAGGAAGCC[A/C]CTTCCATGCCCTCCT	3993
rs374252769	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75550805	AAAAAAAAAAAAAAA[-/C]ACACACACACAAACT	3993
rs374313431	snp	C/T	1.70566e-05	0.00292027	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568488	CAGCCTTTGACGACC[C/T]CTATGCCCTGGTGGT	3993
rs374324740	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75551655	AAGAACTGCCCGCCC[-/C]TTGACTTGTGGCCTG	3993
rs374346369	snp	A/G			stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570181	CCTGCACTCTGAGTG[A/G]CGGCTCGTGGCCTTC	3993
rs374432292	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529973	GACCCTAGTGTGGTC[A/G]CTGACCCGTGCTGAG	3993
rs374460517	snp	C/G/T	4.59762e-05	0.00479441	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558582	TCAAGGGCGGGGCAT[C/G/T]GGAGCTGCAGGAGGA	3993
rs374516090	snp	C/T	0.000101507	0.00712344	intron-variant	LLGL2	GRCh38.p7	17:75574002	CAGGCCTCCTGGGCT[C/T]ATGCACACCTGGGCC	3993
rs374538010	snp	C/T	4.99446e-05	0.00499698	intron-variant	LLGL2	GRCh38.p7	17:75556152	TCAAGCTGTATCCTC[C/T]GTCCCCTCGCTCCCA	3993
rs374571584	snp	G/T	1.6755e-05	0.00289435	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571021	GCCTGTGCAGCGCAA[G/T]ATCGAGGCTCGCTCG	3993
rs374580361	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529855	ACAGAGCAAGACTCC[A/G]TCTCAAACTAATAAT	3993
rs374632397	snp	C/T	0.000132323	0.0081329	intron-variant	LLGL2	GRCh38.p7	17:75558121	GCAGGGGATGGTGTC[C/T]GACCTTCCAGAGCTT	3993
rs374635732	snp	G/T	0.000171562	0.00926021	intron-variant	LLGL2	GRCh38.p7	17:75568749	CCAAACTCTCCCATG[G/T]ACTTCTTGGTCTCTT	3993
rs374705007	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75550512	GGGGCAGGCCGGGCG[C/T]GGTGGCTTACACCTG	3993
rs374809535	snp	C/G/T	0.000151408	0.00869958	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559379	CGTGCGCTGGAGGAC[C/G/T]GGACCATCAGCTCGG	3993
rs374887965	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523297	CCTTCAGCATATCTC[C/T]GTGCTGCAGACAACA	3993
rs374982684	snp	C/T	1.70685e-05	0.00292129	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569098	CGAGAACTTCAGTGC[C/T]CAGGGCGAGGACGAG	3993
rs374987874	snp	A/G	4.95774e-05	0.00497858	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523718	GTTTACCAGGCCGAC[A/G]CTGTGGCCACATTCC	3993
rs375039953	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75572769	AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGT	3993
rs375063107	snp	A/G	1.6591e-05	0.00288015	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574953	TCCCTGCCCCAACCG[A/G]AGAGGCCGGTGCACA	3993
rs375074256	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564406	CCAGCTACGGGGACC[A/G]CCACTGCATCTCAGT	3993
rs375131295	snp	A/G	3.30732e-05	0.00406638	intron-variant	LLGL2	GRCh38.p7	17:75563735	GGATCCGTTCAAGCC[A/G]ATTCCTTTCCTTTCA	3993
rs375193524	snp	A/G/T	0.000221894	0.0105308	intron-variant	LLGL2	GRCh38.p7	17:75563327	CTCTCCTCTTCCTCC[A/G/T]TAGCAACTGGAGAAC	3993
rs375225897	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527528	TTATATTAAAATGAC[A/G]CTACATTCATAAATA	3993
rs375281147	snp	C/T	1.75542e-05	0.00296256	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568992	GGCACGAGGACGGCA[C/T]GGTGCGGTTCTGGGA	3993
rs375372747	snp	C/T			upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524387	GCTTCAGGGACTTCA[C/T]GTTGCCCCAGGATGT	3993
rs375381839	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566506	TCACAGACTGTTGCT[A/G]TAAAGGGCTGGGTGG	3993
rs375381975	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539162	TTCCCAGGCTCAGCA[A/G]TCCTTCCACCTTAGC	3993
rs375429932	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75534490	TGGATTTTTTTTTTT[-/T]CTTTTTTTGAGAAAA	3993
rs375441569	snp	C/T	0.000243555	0.0110326	intron-variant	LLGL2	GRCh38.p7	17:75563006	GGCTCACGGCACTCC[C/T]CTCGCCCAGGTTGCC	3993
rs375452597	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75563959	GGAGACAGGGTAGAC[A/G]CTATTCACGTCTCTC	3993
rs375484130	snp	G/T	0.00039208	0.0139959	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574519	CCGCCCAGGCCAGCT[G/T]GGGTGGGCCCGAGGC	3993
rs375508923	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542880	TGGACAGCCTTCCCC[A/G]AGGTCAGAAGGAGGA	3993
rs375520204	snp	C/T	9.88468e-05	0.00702948	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523355	GTTTCCAAGCAGTGC[C/T]GTCTCTGCAGTACCT	3993
rs375617325	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75555018	TGTCTCTACTAAAAA[-/A]TACAAAAAATTAGCC	3993
rs375625695	snp	C/T	0.000161998	0.00899848	intron-variant	LLGL2	GRCh38.p7	17:75559230	GCAGTGGTCGGCTCA[C/T]GGGCAGCTGTTCTTG	3993
rs375713228	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532337	CCCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACA	3993
rs375713509	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75561440	GACTAGCCTGGGCAA[C/T]ATAGCAAGACCCTGT	3993
rs375713584	snp	C/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75549877	CCTGGAAAGGAGTCC[C/T]AGAGCCCAGGAGAGA	3993
rs375717103	snp	C/T	3.43171e-05	0.00414215	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570977	AGTGCCAAGGCTGAG[C/T]GGCCAGGCCTCCAGA	3993
rs375722979	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528386	TCCCAAAGTGCTGGG[A/G]TTACAGGCGTAAGCC	3993
rs375759610	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550039	GGTATCAGATGTGGG[C/T]GGGGCCGGGTAGGCT	3993
rs375767958	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75540999	GCAAAATGTTTTAAA[C/T]GGAATAGGATGCAGA	3993
rs375811978	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526374	TTTCTCCAGCTGGGG[C/T]GGCTTTGGACACCTT	3993
rs375855324	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524687	CTTTAACGAGAGGGT[A/G]CCTGCTTCGTGCTAT	3993
rs375887642	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572455	GATCACAAGGTCAGG[A/G]GATCGAGACCATCCT	3993
rs375887931	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555109	ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	3993
rs376007135	snp	A/G	0.000189268	0.00972617	intron-variant	LLGL2	GRCh38.p7	17:75556000	CAGCCATGGTGGCGC[A/G]AAGGGGACAGGTCTG	3993
rs376055189	snp	C/T	0.000302842	0.0123016	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573130	TCGAGCCGAGGACTA[C/T]GGGGAGCACCACCTG	3993
rs376078213	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541875	GCTGGGATTACAGGC[A/G]TCTGCCACCACACTC	3993
rs376081119	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75565295	AAACCTGGAGAGGAG[C/T]CCTGCAGGAGCTCTC	3993
rs376105055	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75537351	ATCTGAACCCATCTT[A/G]ACCATTCTCAGGACT	3993
rs376105932	snp	A/G	1.82038e-05	0.00301688	intron-variant	LLGL2	GRCh38.p7	17:75572970	AGCACAGGGCAGGAG[A/G]ACTGGTTTGGCCATG	3993
rs376124751	snp	A/G	7.30861e-05	0.00604464	intron-variant	LLGL2	GRCh38.p7	17:75573290	CAAGGTGTTTGAGCC[A/G]GGCTGGGTGGGTGTC	3993
rs376180173	snp	A/G	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75571831	CGGGCTGCCTGGGCT[A/G]GGTCCAGGGAGTGGC	3993
rs376184032	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75545549	GGTGGGATTGGAGGA[C/T]GAGGCCAGATCCCAG	3993
rs376214744	snp	G/T	1.82221e-05	0.00301839	intron-variant	LLGL2	GRCh38.p7	17:75572966	CAGCAGCACAGGGCA[G/T]GAGAACTGGTTTGGC	3993
rs376285571	snp	A/G	9.38588e-05	0.00684986	intron-variant	LLGL2	GRCh38.p7	17:75573325	CCCCGGGCACTGCAC[A/G]GACGGGAAGGGTGGC	3993
rs376395348	snp	A/T	3.39997e-05	0.00412295	missense, intron-variant	LLGL2	GRCh38.p7	17:75564535	CGGGAGTGGGTGCCC[A/T]GGGTTAGGTGTGGGA	3993
rs376424340	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552350	AAAAACTAGCTGGGC[A/G]TGGTGGTGTGTGCCT	3993
rs376536253	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536393	TTAAAGCCTCGGGAC[A/G]ATGGAATAGAAAAGT	3993
rs376567884	snp	C/G	0.000147556	0.00858815	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574559	GGGCTCAGGGGAGCG[C/G]TGAGAGTGGAGGTCC	3993
rs376587496	snp	A/G	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75569144	AAGGTGAGGCCAGGA[A/G]CCTGGGACCCAGGAA	3993
rs376627352	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75540371	GCCTTGACCTGGGCA[G/T]TGGGTTGATTGGAGT	3993
rs376675954	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575345	TCCACTTGGGGAGCC[A/G]TGTGAATCAAACTGC	3993
rs376704195	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544452	GTGGAGAATGAGGAA[A/G]TCTCTTTGGTTGTAT	3993
rs376728577	snp	G/T	0.000153988	0.00877328	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523234	GCAGACTGAGAAATG[G/T]GACTCCCCTCCCCAG	3993
rs376753735	snp	A/C/G	8.36021e-05	0.0064649	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559325	CTCTACCTGGGCACC[A/C/G]AGAGTGGCAACGTGT	3993
rs376780219	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75548279	ACAATTTTTTTTTTC[-/CT]TTTTTTTTTTTTTTT	3993
rs376790455	snp	A/G	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75568939	TGGGCATCCCGGCTG[A/G]CATCCCTCTCACGCC	3993
rs376794715	snp	A/G	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75547646	CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC	3993
rs376800161	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75535310	ATCAGCAGCGGGCTG[G/T]GGGGAGCACGAGCGA	3993
rs376856563	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75571420	CTAGAGCAGCTGTGA[C/T]GATCGGGGACAGCAG	3993
rs376900486	snp	A/G	5.1409e-05	0.0050697	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571673	TCTCGGCAGGCTCCC[A/G]GCACTGCCCCTCGCT	3993
rs376911831	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555825	TGTCGGGGAAGATCA[A/G]CTCGCAGGGGTGGCC	3993
rs376986902	snp	A/C/G	1.67083e-05	0.00289031	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556069	GCATGGCTTCCCGCA[A/C/G]CAGCCCAGCGCCCTC	3993
rs377004371	snp	C/G	2.3281e-05	0.00341174	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558584	AAGGGCGGGGCATCG[C/G]AGCTGCAGGAGGATG	3993
rs377091364	snp	A/G	0.000101189	0.00711226	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573977	ACTCAGAGTGATGGC[A/G]AGGGTAAGACAGGCC	3993
rs377098784	snp	C/T	0.000102335	0.00715241	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573235	CATCCGCCGGGAGGA[C/T]GTCAGTGGCATCGCC	3993
rs377196255	snp	C/T	7.73007e-05	0.00621646	intron-variant	LLGL2	GRCh38.p7	17:75569917	ATCCTGCGGCCCTGC[C/T]GTCCCTTTGCTGAGG	3993
rs377197296	snp	C/T	1.64749e-05	0.00287005	upstream-variant-2KB, stop-gained, synonymous-codon, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524311	AAGCGGTTGTCTTAC[C/T]AGAGTGGGGATGTCC	3993
rs377256125	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75525929	GGGCTGTCGGGCCAG[A/G]GCGGGAGGGCTGCGC	3993
rs377333287	snp	C/T	0.000153988	0.00877328	intron-variant	LLGL2	GRCh38.p7	17:75569204	TGGCTGCTCACAGGG[C/T]CCCTCCCCTTCTCCA	3993
rs377414113	snp	C/T	3.35154e-05	0.00409348	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571024	TGTGCAGCGCAAGAT[C/T]GAGGCTCGCTCGGCA	3993
rs377431498	snp	A/G/T	1.73655e-05	0.0029466	intron-variant	LLGL2	GRCh38.p7	17:75543542	GACCCCCAGGTTTTC[A/G/T]GCCAAGCAGCTCAGG	3993
rs377453029	snp	A/C/G	1.67108e-05	0.00289052	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568572	CGGTCCAGCTGCCCT[A/C/G]CCTGGCTTCTCTGCA	3993
rs377462870	snp	A/G	1.67778e-05	0.00289631	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563104	AACCAGATCCTGATC[A/G]GCTACAGCCGAGGCC	3993
rs377470630	snp	A/G	5.70163e-05	0.005339	intron-variant	LLGL2	GRCh38.p7	17:75569952	GCTGAGCCACCTGCC[A/G]CCCTGCGCAGGTGCT	3993
rs377519370	snp	C/T	1.72797e-05	0.00293931	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570029	GTGGAGGCCGACCTG[C/T]TGCAGGACCAAGAGG	3993
rs377534101	snp	C/T	0.000167794	0.00915798	intron-variant	LLGL2	GRCh38.p7	17:75556043	ACGTGCTTCTCGTTG[C/T]AGACGGTGGAGCATG	3993
rs377534540	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528859	GTAGAAAGTGTAAAA[C/T]TAGAGAGCAAAAAAT	3993
rs377617590	snp	C/T	1.89925e-05	0.00308154	intron-variant	LLGL2	GRCh38.p7	17:75568945	TCCCGGCTGGCATCC[C/T]TCTCACGCCTGGCAG	3993
rs377617948	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75559426	GTGAGCCCAGAGCCC[A/G]GCTGCTGTTAACTCC	3993
rs377655629	snp	G/T	0.0166325	0.0896639	downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564794	ACTTGAGCCTGGGAG[G/T]TGGAGGTTGCAGCGA	3993
rs377668755	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75555728	GCCCCCATGCCACTG[A/T]GGAGGGCTGGGTCCG	3993
rs377740443	snp	A/G	0.000169986	0.00921759	intron-variant	LLGL2	GRCh38.p7	17:75570543	CACGCACCCAGGTTC[A/G]GCTCAGAGCAGCCAG	3993
rs377740590	snp	A/G	0.000115372	0.00759424	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523643	AGTTCATGTCATAAC[A/G]TTTCTCATTGTATTG	3993
rs377740599	snp	A/G	0.000209974	0.0102442	intron-variant	LLGL2	GRCh38.p7	17:75558494	AGACCACATGATCCC[A/G]TCGTGTGCCCTCGCC	3993
rs386386645	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75527168	TGAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	3993
rs386386646	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75527183	AAAAAAAAAAAAAAA[-/AA]AGTGGCATTTGAGGA	3993
rs386386648	in-del	-/AAAA			intron-variant	LLGL2	GRCh38.p7	17:75572678	CAAAAAAAAAAAAAA[-/AAAA]AAACCAGCATGGTGG	3993
rs386799237	multinucleotide-polymorphism	CCG/GGC			intron-variant	LLGL2	GRCh38.p7	17:75536492	CCGGGCCTAACTATT[CCG/GGC]TGTCTCTAGGGGGTA	3993
rs386799239	in-del	GTCTG/TTTTGGC			intron-variant	LLGL2	GRCh38.p7	17:75547108	TTTTTGTCCAACACC[GTCTG/TTTTGGC]TCAACTCCTTTATAC	3993
rs386799240	multinucleotide-polymorphism	AT/GC			intron-variant	LLGL2	GRCh38.p7	17:75548267	TTTTACAGAAGGACA[AT/GC]TTTTTTTTTCCTTTT	3993
rs386799241	multinucleotide-polymorphism	ATG/GTA			intron-variant	LLGL2	GRCh38.p7	17:75548818	TGGTCTCCTACAGTG[ATG/GTA]TTTTGGGGTGGTATG	3993
rs386799242	multinucleotide-polymorphism	GC/TT			intron-variant	LLGL2	GRCh38.p7	17:75549602	GAGGGCCAGGCTGCC[GC/TT]CACTGCCAGGAATCT	3993
rs386799243	multinucleotide-polymorphism	CGC/TGT			intron-variant	LLGL2	GRCh38.p7	17:75563282	AGGCGATGGGAACGC[CGC/TGT]CTCGGTCCAGCGTGC	3993
rs397790205	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75552137	GTCTTTAAAAAAAAA[-/A]GTCTAGAAGCTGCAT	3993
rs397796252	in-del	-/TT			intron-variant	LLGL2	GRCh38.p7	17:75529148	CAATAGAGTGAGACT[-/TT]GTCTCAAAAAAAAAG	3993
rs397956205	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75540055	GGAGTGCCATCCCCC[-/C]TTTACAGAGGAGCTG	3993
rs398058904	in-del	-/TTT			intron-variant	LLGL2	GRCh38.p7	17:75555305	CTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCGC	3993
rs398070967	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75561212	TTTAGTCTCATAACT[-/CT]GTCTCTGAGAAGTCT	3993
rs527272611	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75548342	GAGTGCAATGGTACC[A/G]TCTCAGCTCACTGCA	3993
rs527336812	snp	A/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75553842	TCTATCCCTGGGACA[A/T]CTGCCCCAGGAAATA	3993
rs527423098	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548013	AGAAAATCTGATATC[C/T]GAAATGCTCCAAAAT	3993
rs527443653	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531444	AGGCCCAAGAGACCA[A/G]TGTTCTTTCTCCTGG	3993
rs527446680	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570824	AGGGTCCCTCTAGAC[A/G]CAGGCCTGGCAGGTG	3993
rs527485244	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571177	GGGGGCATGCCGGGG[G/T]CTGCTGCCTGCCTGG	3993
rs527505147	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525354	CGGCAGCTCCCGGGA[A/G]TTGGAGGGACGGCTC	3993
rs527557447	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75543795	CTGTATCATGGGAAT[A/G]AAACGATCTGCCATG	3993
rs527709032	snp	A/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530350	TACAAAAATTTTTTT[A/T]AAAAATTAGCTGGGC	3993
rs527748223	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547205	AGACGTCTTGTTTCT[C/T]TGGCTTCAGTACTTC	3993
rs527776278	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75540180	CCCCTGGCTCCCTCC[A/G]GGAATGGGCTGAGTA	3993
rs527825854	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75529883	AATAATAATAATTTT[A/T]AAAAAAAGATTTTTA	3993
rs527836276	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534791	TGGCAAAGGACTTGG[A/G]CTCTTGACTGTTTGA	3993
rs527863145	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75544431	CTGGAAAAGGGATGT[C/T]TCCCTGTGGAGAATG	3993
rs527974593	snp	A/G	0.000148907	0.00862735	intron-variant	LLGL2	GRCh38.p7	17:75563726	AGAGTTTGAGGATCC[A/G]TTCAAGCCGATTCCT	3993
rs528003323	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75564289	GTGACTTTGATTGCC[A/G]GCCTGTGGCTGTTGA	3993
rs528085952	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567403	CGGGAGGCAGAGGTT[A/G]CAGTGAGCCGAGATC	3993
rs528105744	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75548051	TTTGAAGTGCCAACA[C/T]GACACTGAAAGGGAA	3993
rs528156921	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75538762	CAGGTCGGGGAGGGC[A/G]TGAAGGTATCTGGAG	3993
rs528180729	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531274	GGTGGCCCATGAGCC[C/T]CTGCCCGCACTGTGG	3993
rs528241315	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532396	GCTGGGATTACAGGC[A/G]CCCGCCACCACGCCC	3993
rs528367430	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567920	TACTCCAGCCTGGGC[A/G]ACAGAGTGTGAAACC	3993
rs528371110	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561692	TTGGGAGGCGGAGGC[A/G]GGTGGATCACCTGAG	3993
rs528374884	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567439	ATTGCACTCCAGCCT[C/G]GGCAACAAGAGCGAA	3993
rs528415167	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562169	CTCCAGCCCTCACGG[C/T]AGCATTCCAGGCCTG	3993
rs528428121	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75528277	CCTGCCATCACGCCC[A/G]GCTAATTTTTTGTAT	3993
rs528482415	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555047	CCAGGCATGGTGGTG[A/G]GCACCTGTAGTACCA	3993
rs528491814	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75535089	CTGGGCTTCCCAGGG[A/C]GACATGGGCACTTGC	3993
rs528567233	snp	A/G/T	0.00319098	0.0398384	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566093	GCAGTCTGATGGAAG[A/G/T]CTTGCCCTGTAGGGA	3993
rs528607359	snp	C/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75560430	AATCTAGTCGGCGGG[C/G]GGGCCCAAGTGCCCT	3993
rs528615423	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526138	GGTGCGGGGGGCACC[A/G]CGGGCAGAGACGGAG	3993
rs528715451	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549262	AAGGAACCATGGGAC[C/G]TCGGGAGGGAGGAAG	3993
rs528748055	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545743	TTTTACCCTTTGGGC[A/G]AGGCAGGTAAGCTCA	3993
rs528800910	snp	A/C	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75549733	CTGCCTCCTTCCCAC[A/C]CCCTGAGGAGTGCCA	3993
rs528880175	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552420	CTTGAACCAGGGAGG[C/T]GGAGGTTGCAGTGAG	3993
rs528902947	snp	C/T	5.31392e-05	0.0051543	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558607	GGAGGATGAGAGCTT[C/T]ACACTGCGTGGACCC	3993
rs529015139	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563575	GGTAAAGGCTTTGTC[C/G]AAAGCCACACAGCAG	3993
rs529110511	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552994	GGGAAAGTGCTGCTG[A/T]CCTGGGAGACGGCTC	3993
rs529133132	snp	A/G	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574179	GCCGAGGAGGGCCCA[A/G]GCGGGGCGCCCTGAC	3993
rs529195586	snp	C/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75547295	GTAACTCCAGTTCAC[C/T]GAGGGCTATGTGCCA	3993
rs529225817	in-del	-/A	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75527011	GTCTCTGCAAATAAT[-/A]AAAAAAAGTTAGCCA	3993
rs529252957	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540461	AGGTCCCAGCCCCGT[A/G]TGGGAAGAGCAGCAG	3993
rs529286209	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75546395	CCTCTGAGATAATGA[C/T]AATCAGAGCCACTCC	3993
rs529425599	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534662	ATTTTTAAGTTTTTT[G/T]CTGAGACAAGGTCTC	3993
rs529559380	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75541228	TGTGCCCTCTTGTCC[C/T]CTCCCTGGAGTCTGC	3993
rs529637261	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534021	GTTCCAGTTTTAGGG[C/T]AGGTAGGAGGCCCTA	3993
rs529752882	snp	A/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75554903	CAAAAAAAAAAAAAA[A/T]TTTTTGGCTGGGTGC	3993
rs529792223	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526275	GCCCCTGCCCCTGCC[A/G]TCTGGGCTGTGTCCC	3993
rs529861259	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75543829	ACCTCGGCACAGGGT[G/T]GTCAAGGAGGTTTAG	3993
rs529885840	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566104	GAAGGCTTGCCCTGT[A/G]GGGACCTGGGGTGCA	3993
rs529892935	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575274	TGGAAAGTGGGAGCC[A/G]GTACCCTGCCTGTCC	3993
rs529967151	in-del	-/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75551093	CTGGGAGACAGGTCA[-/T]TTACACATGAAACCA	3993
rs529987077	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531820	TCAGAGGAAACTGGC[C/T]TTGAATACTCACCCC	3993
rs530048385	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570577	GGGGGCCACACGGCC[C/T]CTGCTCCCCAGGCTT	3993
rs530117018	snp	A/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75569819	AAAAAAAAAAAAAAA[A/T]TGCAGGAGAGCTGGG	3993
rs530136770	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531250	AAGACGAAGTGCTGC[C/G]TGGGACCAGGTGGCC	3993
rs530190301	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535615	ACAGTGGCAGGGTGG[A/G]AGAAGCAGTCTGGCC	3993
rs530250361	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554382	TTTGGGAGGCCGAGG[C/T]AGGAGGATCGCTTGA	3993
rs530260049	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530379	GCATCAGCCAGGCGC[A/G]GTGTCTCACGCCTGT	3993
rs530326843	snp	A/C	0.0023933	0.0345097	downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564844	ACTCAGCCTGGGTGA[A/C]ATAGCCAGACTGTGT	3993
rs530358838	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559634	CTTTGAGGGTCCCTC[A/G]TCTAAAGGCCCCAAA	3993
rs530442469	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528844	GAAAAAGGAAACATT[G/T]TAGAAAGTGTAAAAT	3993
rs530501279	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540267	AGAGAACCTGCTTGT[C/T]TGGGGTGGGGAGCTG	3993
rs530635631	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530353	AAAAATTTTTTTAAA[A/G]AATTAGCTGGGCATC	3993
rs530671783	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533445	GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCATGA	3993
rs530686932	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527605	TTTTTAAACTAAGTT[A/G]ACCAAATTCTTTTTT	3993
rs530709837	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562861	AGGCATGAGCCACCA[C/T]GCTCGGCCATCCACT	3993
rs530752632	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567919	GTACTCCAGCCTGGG[C/T]GACAGAGTGTGAAAC	3993
rs530818895	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75556568	ACCTGTTTTGCAGGG[A/G]TTGTATTGGTGGATC	3993
rs530831020	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541626	CAGTTTCCCCAGAAG[A/G]TGACAGCGCTCTGGG	3993
rs530951153	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75539024	CAGCCTCCCAAGTAG[C/G]TGGGACCACAGGTGC	3993
rs531057106	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75572148	AAAAATGATGGCTGG[A/G]ACTCAGTCTTGTTTG	3993
rs531137502	in-del	-/CTTT	0.00755907	0.0610114	intron-variant	LLGL2	GRCh38.p7	17:75539360	CTGTGCCCAGCCCTC[-/CTTT]CTTTTCAAAATTTTT	3993
rs531150902	in-del	-/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75527788	AACTTTTTTTTTTTC[-/T]TTTTTTGAGGCAGAG	3993
rs531359972	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75547328	CATCAGAGGGGCCAG[A/G]TAGTGGTTAGGGGCA	3993
rs531387838	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75543597	GGATTAAGGTATAGC[C/T]CTTATGTGACTGCCT	3993
rs531431253	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75558700	GCTCTGGAGTGGACT[C/T]ACCCTTTGTGAGGCC	3993
rs531469967	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559104	CTCCTGTCTTGGCAG[A/C]AAGTGACCAATGTTT	3993
rs531541527	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75538848	TCACTGAGACCTGTT[A/G]GCCACCAAAGCCTAG	3993
rs531628017	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75532611	GTATTTTTAGTAGCG[C/G]GGGGGTTTCCACCAT	3993
rs531735499	snp	A/G	6.82815e-05	0.00584261	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573550	GGCTGGTGGAGCCCC[A/G]GTGTCTGGTGGATTC	3993
rs531744285	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554073	TTGAGAGGCCAAGGC[G/T]GGCAGATCACTTGAG	3993
rs531767310	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530328	GGCAACAGTGAGATC[A/G]CGTCTCTACAAAAAT	3993
rs531787875	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549226	CTGCAGCACCAGGAC[A/G]GGGCCACTGAGGACC	3993
rs531799061	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546431	TAGAGTTGGTGTGAG[G/T]ACTACATGAGTTCCT	3993
rs531826279	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75556412	GACTGAGGAGATACA[C/G]GCTTATTTTGTCTCC	3993
rs531889966	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541521	GAGTTTCCCGGCCAC[C/T]TGCTCTTCCCCAGCA	3993
rs531890009	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546898	TACCCAGGGCTGGAG[C/T]CTGGAGCGGCACGTG	3993
rs531989692	snp	C/G	0.00716266	0.059414	intron-variant	LLGL2	GRCh38.p7	17:75526491	ATCTTGCCAAAGAAA[C/G]TGTGTCTTAGTTTGT	3993
rs532070651	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529884	ATAATAATAATTTTT[A/T]AAAAAAGATTTTTAG	3993
rs532108359	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538681	TCAGTGTGTCCAAAC[A/G]TGGCCAGGTCCAAGG	3993
rs532189512	in-del	-/A			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564863	CCAGACTGTGTCTCA[-/A]AAAAAAAAAAAAAAA	3993
rs532193752	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75549603	AGGGCCAGGCTGCCG[C/T]CACTGCCAGGAATCT	3993
rs532209301	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544228	TTGTGAGGTAATGAT[C/T]TTCTCACCTCTGCTT	3993
rs532227339	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75528467	AAAAAGGCCAGGCGT[A/G]GTGGCTTACACCTGT	3993
rs532282482	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532335	AGCCCACTGCAAGCT[C/G]CGCCTCCTGGGTTCA	3993
rs532283333	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544591	GTTAAGGGCGTACGT[A/G]GGGTGAGGTAACTTA	3993
rs532287191	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75527420	TGTGGGGGCTCCTGG[A/G]CAGGGTTTCCGGGGT	3993
rs532298961	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566626	GCCATATTGACAGGA[A/G]TAGGCAGGAGGCCAG	3993
rs532340816	snp	A/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75551587	TTTGTCTTCCTCTGA[A/G]TTAGAGGAAAGATGC	3993
rs532354034	snp	A/C	0.00438332	0.0466095	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525194	GCGCCCCCCCGCACC[A/C]CCCCCCGAGGAAAGG	3993
rs532384954	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75559730	CAGGGGCTCCGCAGC[A/G]GGGAAGTCGGGCCCA	3993
rs532394871	snp	C/T	0.000155789	0.00882441	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570022	GGAGCAGGTGGAGGC[C/T]GACCTGCTGCAGGAC	3993
rs532427779	snp	A/G	0.000284207	0.0119173	intron-variant	LLGL2	GRCh38.p7	17:75572076	CAAGGTGCCACACGG[A/G]CAGCGGCGGGTCTCC	3993
rs532467189	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567299	TGAAACCCTGTCTCT[A/T]CTAAAAATAAAAAAT	3993
rs532486561	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532862	GCCCTGGCCTTGGCC[A/G]GAGACTTGAGGACAG	3993
rs532491104	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570768	CTACAACATGCTGGG[A/G]GCCCAGGCAGGCTCC	3993
rs532538591	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531299	CTGTGGGAGATCTGC[A/G]CATCTCTGGCAAGAG	3993
rs532551619	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526019	TGTAGAAAGTTCTGC[A/G]GGAAACTTCTCTGCC	3993
rs532555334	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565881	TAATGAGCAACTGCT[A/G]TATGCCAGGCCCTGT	3993
rs532620034	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560308	AACACTTTGCAGGAT[G/T]ACAGGTACCACAGTG	3993
rs532734207	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554981	CAGATCATGAGGTCA[A/G]GAGATAGAGACACGG	3993
rs532782579	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557615	CCCTCTGCCCGGTGT[A/G]GGGGAGGGGTATGGA	3993
rs532807896	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563279	TGCAGGCGATGGGAA[C/T]GCCGCCTCGGTCCAG	3993
rs532813559	in-del	-/TTTTTTTTTTTTTT	0.16028	0.233346	intron-variant	LLGL2	GRCh38.p7	17:75533300	CACCGCACCTGGCCC[-/TTTTTTTTTTTTTT]TTTTTTTTTGAGATG	3993
rs532834848	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542315	CAGTCAAAGCACTCA[A/G]CACTGGGCTGCCCTG	3993
rs532866412	in-del	-/TT			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541745	TTTTTTTTTTTTTTT[-/TT]GAGATACTGTTTTTG	3993
rs532946344	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536361	AGAGTTTGCCAAGCC[C/T]GCTCCCTGGCCCTGC	3993
rs533095656	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552333	GTCTCTACTAAAAAT[A/G]CAAAAACTAGCTGGG	3993
rs533150917	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545304	TGCCTTCTTCTTTCC[A/G]TTCATATGCAAGAAG	3993
rs533305987	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550375	CTGAACCCTAAACAA[C/G]GGGGGAGTCACCACC	3993
rs533312652	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75533516	TCATCATGTTGGCCA[A/G]GATGGTCTCGATCTC	3993
rs533313570	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75533868	GGCCTCTGCCAGAAG[G/T]TGACATTTGAGCAAA	3993
rs533326521	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567003	AAACCAGGGGCCCTG[A/T]TGAGGCTGCCCAGGT	3993
rs533337391	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75541148	TCCTACTGGCACCTC[C/T]TCCCAGCCCCCAGTT	3993
rs533338109	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550850	GCACAGCCAGAGGTG[C/T]CCATGGAGCCTTCGT	3993
rs533363736	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567988	GGTTTAATCATCCAG[C/T]GCACATTTATTGAGC	3993
rs533373495	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533960	GATGAGGCCAGCACA[A/G]TCCCCACCTCCTGGA	3993
rs533447071	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540380	TGGGCAGTGGGTTGA[C/T]TGGAGTGAGGGGATA	3993
rs533530424	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572643	GCCCTCCAGCCTGGG[C/T]GACAGAGCGAGATTC	3993
rs533534277	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530715	CAATTACATGGGATC[A/G]TAGGAGGATCGCTTG	3993
rs533568617	snp	A/G	8.44188e-05	0.00649633	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573087	GCTCAAGAGTGCGGC[A/G]GGTCAGCGTGGCCCA	3993
rs533606852	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75547430	GACGCATTACTTAGC[C/T]TCTCTGTTCTTTAGT	3993
rs533634868	snp	A/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75527270	CAGCTTTATTTTATG[A/T]ACTGGGATTTGGGGT	3993
rs533638745	snp	A/C	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75545803	GATAGGTGACAGCCC[A/C]GAAGGAAGGGACTGG	3993
rs533640410	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541761	TGAGATACTGTTTTT[G/T]CTCTGTTGCCCAGGC	3993
rs533692136	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543047	CTTTCTGCTTAGCTG[A/G]AGTTTCATGGTTTCT	3993
rs533720875	snp	A/G	1.73465e-05	0.00294499	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564551	GGGTTAGGTGTGGGA[A/G]GCATGGGGCAGGACC	3993
rs533821090	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536376	CGCTCCCTGGCCCTG[A/C]TTTAAAGCCTCGGGA	3993
rs533838330	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542327	TCAACACTGGGCTGC[C/G]CTGTCTCTACCTGTC	3993
rs533880326	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530908	CGGCTTCTCCTAAAT[A/G]GACCTTGCATTCCAG	3993
rs533964624	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523147	TCACGCCACTATACT[C/G]CAGCCTGGGTGACAG	3993
rs534017835	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75571490	GTTCTCCCCTGCTGT[A/G]TCACAGCAAGGGCTG	3993
rs534065909	in-del	-/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75551489	AAAGAAGGTGGGGAT[-/G]GGGGGGAGGGGTGGC	3993
rs534079297	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75564076	TTTAGTTGGCAGCCC[C/T]GTTTCTTCAGACAAA	3993
rs534140921	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524065	ACAGGCTAAGAGTGG[G/T]GAGCACCTTGCTCTT	3993
rs534188459	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75557878	AGGGTGGCAGCCTGA[C/T]AGTTGCCAGGGTAGG	3993
rs534272190	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534272	GCAACAGAAAGGAAA[C/T]TTCAGGAGGAGTCTA	3993
rs534366232	snp	A/G			missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574242	CTGGTGATGGAGCGC[A/G]CTCTGCTCAGTGATG	3993
rs534406258	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566215	ATGTGGCCAGCGCCA[G/T]ATCGTATAGAGCCGT	3993
rs534526317	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552644	AGTTCAGACATTAAA[A/T]CTTTTTTGGAAGTAC	3993
rs534554646	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526808	AGGTGACAAGGAAAC[A/G]CTGGTAGGAAGAGCA	3993
rs534584602	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566761	GGAATCCTGGAGAAG[A/G]TAGTGGCAAGAGGGT	3993
rs534603575	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75550684	TAGCTACTCGGGAGA[C/T]TCAGGTGGATCACTT	3993
rs534610908	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528652	CTGAAGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	3993
rs534689305	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531941	ACCCTTCAGGAATTC[A/G]GCAGAGACTGGAGCC	3993
rs534715229	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548587	GGTAGATCACCTGAG[G/T]TCAGGAGTTCGAGAT	3993
rs534821502	snp	G/T	0.0170251	0.090679	intron-variant	LLGL2	GRCh38.p7	17:75554485	GTGTGGCAGGTGTGG[G/T]GGTGCATGCCTGTAG	3993
rs534913065	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555866	GGGCAGAGTCACAAA[G/T]GGACAGGGGGTGGGG	3993
rs534915353	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75546856	GTCCAGCAGACAGGC[A/G]GAGGGCAGGTCCAGC	3993
rs534948463	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549917	TCCCCTACTCCAGGC[C/T]AACGTTGCAGTCTGG	3993
rs534963232	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75543950	CCCTTCTCAAATTGC[C/T]CCTGAAGGAAAATGC	3993
rs535008352	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575015	TTCCACAATGCAGCT[A/G]CTCTGGGCCTCGGGA	3993
rs535013577	snp	A/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537455	TCCTAGCACTTTGTG[A/G]GGCCGAGGTGGGCAG	3993
rs535102754	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75546472	AAGGCCACGTCTGGC[C/T]GGCGGCTGCAGTGTC	3993
rs535184986	snp	A/G	0.00755907	0.0610114	intron-variant	LLGL2	GRCh38.p7	17:75554755	TTAGCCGGGCGTGGT[A/G]GCGGGCGCCTGTAGT	3993
rs535189011	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538117	CGCCCAGCCTGGAAG[A/G]GGGGCCGGGCTGATT	3993
rs535200382	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531580	TCCTGGGGCGAGGCA[C/T]GCCAGGTCTGCTTGG	3993
rs535206115	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75546128	AGGGAGGGGATGGGG[A/G]GGGGAGGCGGGTGTG	3993
rs535426858	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542192	TGATGGTTAATTTTT[A/G]CCACCTCCCAAGAAC	3993
rs535699109	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541650	CTCTGGGGGCTGGTT[C/T]CTGGTATTCGGTTTT	3993
rs535729702	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533548	TGACCTCATGATCTG[C/T]CCGCCTCGGCCTCCC	3993
rs535755722	snp	C/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561861	CCGGAGGTGGAGGTT[C/G]TGGTGAGCCGAGGTC	3993
rs535791240	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75528477	GGCGTGGTGGCTTAC[A/G]CCTGTAATCTCAGCA	3993
rs535806941	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75572314	ACAAGGGCAGGAGTT[C/T]GAGATCAGCCTGGCC	3993
rs535838827	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531008	TGTGGTGGGGATGTC[A/G]GAGAGTGCAGGATTA	3993
rs535896720	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567634	ACAGAGCAAGACTCC[A/C]TCTCAAAAAAAAAAG	3993
rs535899106	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572752	AGAATTGCCTGAGGC[A/G]GAGGTTGCAGTGAGC	3993
rs535900388	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545384	GAATCTGATTAGGCC[C/T]CTGCCCTCCACTTTT	3993
rs535968112	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75536478	GTCTCCCCGCCTTTC[C/T]GGGCCTAACTATTCC	3993
rs535971227	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75534075	TGGATGGCCTGCCCA[C/T]GCCAGCCCCAGGCAG	3993
rs536022166	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562610	GTCTCACTCTGTCAC[C/T]CAGGCTGGAGTGCAG	3993
rs536058810	snp	A/G	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75554044	TGATGGCTCACACCT[A/G]TAATCCCAACACTTT	3993
rs536121845	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524744	TCTTTTCTGCTGTTT[C/T]TGTATGTACTGGGTA	3993
rs536141789	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568256	GGTGTATCCCCCCAG[G/T]AGCCCTGTGCCAGGG	3993
rs536211924	snp	C/G	0.000131525	0.00810835	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570424	CTCAAGAAGTCCTTG[C/G]GTCAGTCATTCCGCC	3993
rs536214273	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563822	GTAGGTATCCATGCT[G/T]GTCCTCTTTCCTCTC	3993
rs536311399	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543348	GGGCCGGGCCTAATC[A/G]ATACCTGAGTGCCAG	3993
rs536330043	snp	C/T	6.80029e-05	0.00583068	intron-variant	LLGL2	GRCh38.p7	17:75563478	GGTCAGTGTTTCACC[C/T]GCCGGGCAGGGCCCA	3993
rs536457666	snp	C/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75560528	TTTCACTCTTGTTCC[C/G]CAGGCTAGAGTGCAA	3993
rs536503782	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559171	CTTATGGGCTTGTTT[C/T]CCGAGGAGTCAGGGG	3993
rs536526366	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531481	TGCTTTGAGCAGCAC[A/T]GGCAGCCTGGACTCA	3993
rs536578325	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75557356	GAGGGCTCTGCCTGG[C/T]AGGGACAGTCCTTCC	3993
rs536603609	snp	A/C/T	9.99507e-05	0.00706869	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523741	CACATTCCGAAAGAA[A/C/T]AACCCTGGCAAACCC	3993
rs536615094	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555938	GAGGAACCGGAAAGG[G/T]ACCGAAGCCCTGCTT	3993
rs536663741	in-del	-/GC	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75547113	GTCCAACACCTTTTG[-/GC]TCAACTCCTTTATAC	3993
rs536724825	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530031	AAAGGTCACTAGCAC[A/G]TGTGGCCTGCCACAC	3993
rs536733764	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561261	ATAAGAATGATCATT[A/G]TAGGGCTGTTTTTAA	3993
rs536882677	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574377	TCCATGGGCACCCAC[A/G]GAGAAAGGGGGTGGA	3993
rs537146365	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75559850	TAAAAAGCCTTGACC[A/G]CCACAGGCATGTGGG	3993
rs537184110	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544010	CTTCTGGCTCCGGCC[G/T]GGGTGAGTGGGGAGA	3993
rs537323275	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75571534	TTGGGGTCTTCTATG[C/T]TGGGGCCTGTGTGGT	3993
rs537351203	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550630	TCTCTACAAAAAATA[C/G]AAAAATTAGCCAGCT	3993
rs537373098	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528821	AAGGCAATAGGAGCC[C/T]ATAGTGGGAAAAAGG	3993
rs537379301	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75545490	CAGGGGATTCAGGAG[C/T]GGGGTAGACTCATCC	3993
rs537472865	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542210	ACCTCCCAAGAACGC[A/G]AAATCCTTCAAACCT	3993
rs537495769	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552528	CAACATATGCAAAAT[A/C]TTTTGACGTGTGATT	3993
rs537583299	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75554690	ATGGGCGGATCGAGA[A/C]CATCCTGGCTAACAC	3993
rs537594053	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75564013	CATTCTTGCTCCTTT[C/T]TTCCACCTTCCCAGA	3993
rs537611952	snp	G/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75569837	CAGGAGAGCTGGGGT[G/T]GGACAGAGGCCTTTG	3993
rs537618619	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571838	CCTGGGCTGGGTCCA[A/G]GGAGTGGCTCCAGCC	3993
rs537728468	snp	A/T	0.000399281	0.0141238	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574251	GAGCGCGCTCTGCTC[A/T]GTGATGAGAGTGAGT	3993
rs537751983	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538924	AGAAACAAGAGTCTC[A/G]CTCTGTGGCCCAGGC	3993
rs537799584	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539745	CCTGAGTAGCTGAAA[C/T]TACAGGAGCACACTA	3993
rs537816031	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534091	GCCAGCCCCAGGCAG[G/T]TGGTCCATCTTCTCC	3993
rs537820115	snp	A/G/T	3.40769e-05	0.00412765	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573233	TGCATCCGCCGGGAG[A/G/T]ACGTCAGTGGCATCG	3993
rs537887054	snp	A/G			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575141	TTTTGTAGTGGGCTG[A/G]GTTTTAAGTTATAAA	3993
rs537888835	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75573734	GGAGGCACCTCCCCA[C/T]GAGCTCAGCCCACCC	3993
rs538064097	in-del	-/C	0.00716266	0.059414	intron-variant	LLGL2	GRCh38.p7	17:75551652	TAGAAGAACTGCCCG[-/C]CCCTTGACTTGTGGC	3993
rs538130709	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534969	AGTCATGCCCCCATT[C/T]CCTCTGGTTTGTGTT	3993
rs538204588	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528534	GCCTGAGGTCAGGAG[G/T]TTGAGAGCAGCCTCA	3993
rs538209493	snp	C/T	4.02067e-05	0.00448349	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568439	GCTGGGCTGCTTCCT[C/T]CTGGCCCCGGCCCCT	3993
rs538219321	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565590	GGCCACACTCCCCGG[G/T]CTAACTGAGTTACCT	3993
rs538256095	snp	C/G/T			intron-variant	LLGL2	GRCh38.p7	17:75551491	AGAAGGTGGGGATGG[C/G/T]GGGGAGGGGTGGCCA	3993
rs538270084	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75544840	AGGACATTTGCCTCT[A/G]GAATTAGGGCTTTCC	3993
rs538303641	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540692	CACAGCCCTTCTGAC[A/T]TGGGGTCCAGTCCGA	3993
rs538317718	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572803	CCAGCCTGGGCGACA[C/G]AGCAAGACTCCATCT	3993
rs538447847	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75551910	AAGGCGAGGAGATCA[C/T]TTGAAGTCAGGAGTT	3993
rs538470552	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75549415	TGCTTGCCCGGCTGC[C/T]GCAGAAGCACCTGCC	3993
rs538530991	snp	A/G	6.81896e-05	0.00583868	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563039	AGGAGGCCCGCCACC[A/G]GCGTGTGTTCGAGAT	3993
rs538590346	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75531860	CCCAGGAACCACAGC[A/G]AATTCTTGAGCTAGG	3993
rs538592515	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75571336	TTAGAAGCATGGCCT[C/G]AGACCCATCACTTAG	3993
rs538633506	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566164	CCAATGAGGTAGGGG[C/T]GAAGAGAGGGCAGAA	3993
rs538723876	snp	C/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537452	TAATCCTAGCACTTT[C/G]TGGGGCCGAGGTGGG	3993
rs538736341	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523986	GCATTTTAGGGTAGT[C/T]TTTCTCCAATGCCAT	3993
rs538799510	snp	G/T	3.53301e-05	0.00420283	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574643	ACATCGAGCCGCCGT[G/T]GGGTGCAGCCTCAGC	3993
rs538879118	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543023	GAGGAAGAGGCTTGC[A/G]AAGTTTCCCTTTCTG	3993
rs538902010	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526319	TGCCTCCTAATCCCC[G/T]GACGCAGGAAGCCCG	3993
rs538923361	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560641	ACAGGCATGCGCTAC[A/C]ACACCCAGCTAATTT	3993
rs538924063	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75533156	AGGCTCCCGCCACCA[C/T]GCCCGGCTAATTGTT	3993
rs538961632	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75555186	CATCTCAAAAAAAAA[A/G]AAAATAGACCTGCAA	3993
rs538991992	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541461	TTTCCCAGCCGGTGC[C/T]TGTTCTCTGAACCCC	3993
rs539140021	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556257	TAAAATGAGGGACTT[C/T]CCTGATTTCCAGTTT	3993
rs539148732	snp	A/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75562462	GTCACTGCCTTGCCT[A/T]GCCTTATAATTGTAC	3993
rs539149290	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553446	CTAGACTGACTGATG[C/G]GGGAGGCAGGTAGCA	3993
rs539178819	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556937	GGGAGGCTGAGATGG[A/G]AGAATCGTTTGAACC	3993
rs539208239	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572920	TTTGTCAGGACACCG[A/G]GAGGCATGTGGGGAG	3993
rs539209366	snp	C/G	0.00993419	0.0697739	intron-variant	LLGL2	GRCh38.p7	17:75536494	GGGCCTAACTATTCC[C/G]TGTCTCTAGGGGGTA	3993
rs539211196	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75543898	ATAATGTTCCAGGTC[C/T]CTTGGGGCCCTGGAG	3993
rs539238301	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75539382	TTCAAAATTTTTATT[C/G]TTCCATGTAAATTTG	3993
rs539269878	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530370	ATTAGCTGGGCATCA[A/G]CCAGGCGCGGTGTCT	3993
rs539286949	snp	C/T	1.743e-05	0.00295206	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573252	TCAGTGGCATCGCCT[C/T]CTGCGTCTTCACCAA	3993
rs539357301	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548453	CGGCTAAAGGACAGC[C/T]TTTCAGAGCTACTCC	3993
rs539367300	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75562743	CCAGCTAATGTTTTA[C/T]ATTTTTAGTAGAGAC	3993
rs539488839	snp	A/G	0.000102505	0.00715833	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571929	GATGCACCGGGCGCC[A/G]GTGGTGGGCATCCTG	3993
rs539614629	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75533594	CAGGCATGAGCCACC[A/G]CGCCCAGCCCGTTCA	3993
rs539730421	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539685	CGATCTCAGCTCACT[A/G]TAACCTCCACCTCCC	3993
rs539784695	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540724	TTCTGCCGCTTCCTA[C/T]TTGGTGACCTTGACA	3993
rs539793152	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75533100	TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	3993
rs539810850	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530274	TTGGGAGGTGGAGGA[A/G]GGAGGATTGCTTGAA	3993
rs539874143	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549875	GACCTGGAAAGGAGT[C/T]CCAGAGCCCAGGAGA	3993
rs539946701	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75535099	CAGGGCGACATGGGC[A/G]CTTGCAAAGCGGCTA	3993
rs539986807	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567544	CTTGGGAAGCTGAGG[C/G]AGGAGAATCGCTTGA	3993
rs540104287	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572212	AAATAAGTGAGGGGG[C/G]AGTCTCGTGTGAGGA	3993
rs540119342	snp	C/T	0.000639156	0.0178653	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558525	AGTGCCAGCTGGTCA[C/T]CCTGCTGGATGACAA	3993
rs540183946	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75553072	CTGGTGGGGCCCCTG[A/G]GGGAGCTTGTCCTGC	3993
rs540348479	snp	A/G	1.70064e-05	0.00291597	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569113	CCAGGGCGAGGACGA[A/G]TGGCCCCCACTCCGC	3993
rs540354350	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528678	GGGAGGTGGAGGTTG[C/T]GGTGAGCCAAGATCA	3993
rs540477851	in-del	-/T	0.32955	0.237006	intron-variant	LLGL2	GRCh38.p7	17:75539609	CCATTTTCTGGTTAC[-/T]TTTTTTTTTTTTTTT	3993
rs540492454	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75530738	ATCGCTTGAGCCCAA[C/G]AGTTTGAGGCTGCAG	3993
rs540602841	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557355	AGAGGGCTCTGCCTG[G/T]CAGGGACAGTCCTTC	3993
rs540639474	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75551470	TTCTAAATCAGCCTT[G/T]GGAAAAGAAGGTGGG	3993
rs540716400	snp	A/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75556768	TTTAATTTAAAAAAA[A/T]TTTTTTCGGCACTTT	3993
rs540865119	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573417	CTAGCCCCTACTCCC[C/T]CAGGTGGGGAGGCAG	3993
rs540920345	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551989	CAAAAATTAGCTGGG[C/T]GTGGTGGTGCATGCC	3993
rs540962643	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75544105	TACCAGAAGGCCCAC[A/G]GGGCTTCCCTTCAGG	3993
rs540996219	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554821	GTGAACCTGGGAGGC[A/G]GAGCTTATAGTGAGC	3993
rs541036933	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548898	CTTCAAACGGTGCCT[A/G]ACACAGGTCGACGCC	3993
rs541110704	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525568	GCGGATTGGCAGGAG[C/T]GCAGCCCCCACCCCC	3993
rs541198185	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543246	GCGTGGGGAAGCCAG[A/G]GTGCATGGGCGGTCA	3993
rs541236482	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525119	TCCAACCTCCTCCCT[C/T]GCTTGTGCTAAAAAT	3993
rs541307351	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75559579	CTACTGAGAACCTAT[C/T]GGCCTGTCATAGGTT	3993
rs541346288	snp	C/T	0.000128725	0.00802159	intron-variant	LLGL2	GRCh38.p7	17:75570530	GGCTGCGGCCGGCCA[C/T]GCACCCAGGTTCGGC	3993
rs541349743	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544488	TTATTGATTTGAGAA[C/G]TGTAGAAGTCAGCTT	3993
rs541420596	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572550	GGCACCTGTAGTCCC[A/C]GCTACTCAGGAGGCT	3993
rs541455794	snp	A/G	3.58218e-05	0.00423197	intron-variant	LLGL2	GRCh38.p7	17:75572999	TGGGCATGAACAACC[A/G]CCCCACGCCCCCAGG	3993
rs541495865	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542137	CTTCTCCCACGCTGC[C/G]CAGATTACATGGGAT	3993
rs541517924	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75551984	AAATGCAAAAATTAG[C/T]TGGGCGTGGTGGTGC	3993
rs541701282	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75559566	TCCTACCTGTCACCT[A/G]CTGAGAACCTATTGG	3993
rs541727805	snp	A/G			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569996	AATGACGAGGCAGCG[A/G]AGCAGGCTGTGGAGC	3993
rs541739454	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530623	CCACTGCACTCCAGC[C/T]TGGGCGACAGAGCGA	3993
rs541753930	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75531207	CCTCTCCTGCCAGGA[C/T]TTCCTGGCCCCGGGA	3993
rs541777963	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532573	GGATTACAGGTATGC[A/G]CCACCACACCTGGCT	3993
rs541819914	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560992	GCACGCCATCACACC[C/T]GGCTTATTTTTGTAT	3993
rs541839191	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533423	CATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG	3993
rs541840850	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529261	GAGCACAGTGGCGTG[A/G]TCTCAGCTCACTGCA	3993
rs541905285	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532778	ATTCTCTGGGGGTCC[C/T]GGAGCTTTGGTTAAA	3993
rs541914284	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75532261	CCAGCTAATTTTTTG[C/T]TTGTTTTGAGACGGA	3993
rs541922832	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526575	CTAACCAGGGGAGCT[G/T]TAGAGTGGCGCTTTG	3993
rs541925045	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540219	CTGTTCATACCAGGC[A/G]TCTCTAGGCCTGGCT	3993
rs541926623	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532572	GGGATTACAGGTATG[C/T]GCCACCACACCTGGC	3993
rs541992118	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550208	ATGCCCCGTCCCGCC[C/G]TCTGTCCTGAGTGCA	3993
rs542026747	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550728	GGAGGTTACAGTGAG[C/G]TGAGATCGTACCACT	3993
rs542028745	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75545135	TGCCCCCTTGCACCA[A/G]GTTCTGTCTGTGCAG	3993
rs542032401	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556364	GTGGGATGCGACCCT[A/G]TCCTTTGCAGGAGGA	3993
rs542055984	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557479	AAAAACCGGATCAGG[C/T]TGGGCACCCCGCCAG	3993
rs542305083	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75559028	CCATCCGCACCCCGT[G/T]TTATGCTGGAGGGTC	3993
rs542318241	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530480	ACAGTGAAAACATGT[A/C]TCTACTAAAAATACA	3993
rs542387447	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547697	GGGTGTGGTGGCACA[C/G]GCCTGTAGTCTCAGC	3993
rs542426201	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543283	AGCTGGCCTGGCCCC[A/G]GGGTGGCAGCCTACT	3993
rs542426233	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548299	TTTTTTTTTTTTGGA[C/T]GGAGTTTAGCTCTTG	3993
rs542469170	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539671	GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGT	3993
rs542544356	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553680	GCTGTTCTCACCTAG[C/T]TCTGCAGGGTCACTA	3993
rs542555436	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75538778	TGAAGGTATCTGGAG[A/G]AAAGTGACCCAGGCA	3993
rs542658473	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75559238	CGGCTCACGGGCAGC[C/T]GTTCTTGTCACAGGG	3993
rs542722965	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563596	CACACAGCAGGGTTC[A/G]CCTCACCCAGTTTCT	3993
rs542765521	snp	C/G	2.2772e-05	0.00337424	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570090	CAGCCCGCTCAGGGC[C/G]CGTGCGCTTTGAGCC	3993
rs542779184	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554266	AAGATCGCACCATTG[A/C]ACTCCAGGCTGGGTG	3993
rs542810043	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573853	GGCTCTCCGGCTCAG[A/G]ACAGGCTGCGCCATT	3993
rs542879950	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535114	ACTTGCAAAGCGGCT[A/G]CAGGCGTCTGAGTTG	3993
rs542986071	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542451	TTTCCCAAGGACGGG[A/C]CTTGCTGTCCTGTGG	3993
rs543053861	snp	C/G	0.0170251	0.090679	intron-variant	LLGL2	GRCh38.p7	17:75546861	GCAGACAGGCGGAGG[C/G]CAGGTCCAGCGGACG	3993
rs543059753	snp	A/C/T			intron-variant	LLGL2	GRCh38.p7	17:75536026	CCACAAGGCAGCAAG[A/C/T]CTTTTGCGGCCCGGC	3993
rs543137169	in-del	-/CTCT	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75536647	CTTCTCTCTTTGATC[-/CTCT]TATCCACCCTGCCTA	3993
rs543214167	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75546179	TGACCTGGGTAGGTG[A/G]TGGTGCCAGGCCTTG	3993
rs543251004	snp	C/T	6.71242e-05	0.00579289	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563127	CCGAGGCCTCGTTGT[C/T]ATCTGGGACCTACAG	3993
rs543294412	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572400	CAGGCGCGGTGGCTC[A/G]TGCCTGTAATCCCAG	3993
rs543364091	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75532303	TTGCCCAGGCTGGAG[C/T]ACAGTGGCGCGATCT	3993
rs543379778	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525542	GGCCCCGCCCCGCGC[C/T]TCCCGGGGCCGCGGA	3993
rs543455147	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544548	AGAAGCTGGATGGCC[C/G]TGTGCCTGTCGCCCA	3993
rs543493919	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555358	GCCTGCCGGGTTCGC[A/G]CCATTCTCCTGCCTC	3993
rs543509154	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567160	GAGTAGCAGGGAAGA[A/C]AAGCACTTCAAAGAG	3993
rs543559225	snp	C/G	1.70746e-05	0.00292182	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572007	CCATGATCTGTCGAA[C/G]AGCCCTGACATGCAG	3993
rs543565968	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536910	TGGGCTCACTGCAAC[G/T]TCCACCTCCCGAGTT	3993
rs543568054	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75574726	AAGGGCTGGGAGGAA[A/G]AGCCCCGGCCCCACT	3993
rs543612024	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560872	AGAGTCTTACTCTGT[C/T]CCAGGCCGAAGTGCA	3993
rs543657571	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554929	GGTGCGGGTGGCTCA[C/T]GCTTGTAATCCTAGC	3993
rs543687189	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75565815	AGCTCTCACGTAATG[C/G]TTCTGCTGTGCCGGG	3993
rs543740623	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75545055	TCTGCCTCCAGTCTT[G/T]CGCTTTGAAAAGGTG	3993
rs543752470	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539224	CACCATGCCCAGCTA[A/G]TTTTGTTTTTATTAT	3993
rs543755909	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575147	AGTGGGCTGGGTTTT[A/G]AGTTATAAATGTTAA	3993
rs543814135	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75573372	ACGGCCAGACTGGAT[A/G]GGCCTTAAGCGGAGA	3993
rs543826446	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537625	ATTGCTTGAACCTGG[A/G]AAACACAGTTGCAGT	3993
rs543856049	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540931	ATGCTGGGGTTTAGG[A/G]AGGATTTTCTTGTCT	3993
rs543885553	snp	A/G	0.000182951	0.00956252	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568661	CGGATCATTGCCGCC[A/G]GCAGCCGGCAGAACG	3993
rs543927166	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75538261	CATGGAGGAGGGAAC[G/T]GGGGGTGGGCAGGCC	3993
rs543970835	snp	A/G/T	0.00100057	0.0223458	intron-variant	LLGL2	GRCh38.p7	17:75558036	GGGTCCTGCTGCCTC[A/G/T]GGGGAGGGCAGCCCC	3993
rs543972499	snp	C/T	1.71281e-05	0.00292639	intron-variant	LLGL2	GRCh38.p7	17:75563496	CGGGCAGGGCCCACC[C/T]CCAGTGCCTCCTGGA	3993
rs543997088	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526394	TTGGACACCTTCACA[A/T]GACAGTGCGGAGACC	3993
rs544002528	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75558399	CTGGGGCTCATGGGC[C/T]ACCCTGGGAGTGGCC	3993
rs544061914	in-del	-/CTGGCCCTGCAAGGCTTTGGA			intron-variant	LLGL2	GRCh38.p7	17:75560071	CAGGGTGCTGGGCCC[-/CTGGCCCTGCAAGGCTTTGGA]CTGGGCCTGGGACAC	3993
rs544118675	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525187	GAGGTGGGCGCCCCC[A/C]CGCACCCCCCCCCGA	3993
rs544127293	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525709	GCCGCGCCGGAGGTG[A/G]GCAGGAAGGAGACGG	3993
rs544146253	snp	A/C/T	0.000166596	0.00912535	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568657	GGAGCGGATCATTGC[A/C/T]GCCGGCAGCCGGCAG	3993
rs544148129	snp	A/G	6.72687e-05	0.00579912	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573167	CTTACCAACCTGGGC[A/G]ACATCCAGGTGGTCT	3993
rs544169101	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528881	GCAAAAAATTAGGCC[A/G]GGCAAGGTGGCTTAT	3993
rs544244578	snp	A/C/G	3.43143e-05	0.004142	intron-variant	LLGL2	GRCh38.p7	17:75556006	TGGTGGCGCGAAGGG[A/C/G]ACAGGTCTGCAGGCC	3993
rs544306487	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533776	GATACGGGCTATAGG[A/G]TAAAAAGAACTAGAG	3993
rs544321281	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75537422	TCCCAGGCTGGGTGC[A/G]GTGGCTCACGCCTAT	3993
rs544367744	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533252	GATCTGCCCGCCTCA[A/G]CCTCCCAAAATGCTG	3993
rs544382239	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75528152	ACAGAGTCTCGCTCT[A/G]TCACCCAGGCTGGAG	3993
rs544457898	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75547536	GCTATGAATTAAATT[A/G]ACGAGAGGCGGGGCG	3993
rs544532580	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75545770	CTCAGAGCAGTTAGG[A/C]GACATTGCCCCGACT	3993
rs544568071	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557311	GTCTTCCAAATTCCA[C/G]CCCCACTCCCACAGG	3993
rs544595208	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556410	TGGACTGAGGAGATA[C/T]AGGCTTATTTTGTCT	3993
rs544606786	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551425	TGGCAGGAAGGGATA[C/G]AAAGCTTAGTGGGTC	3993
rs544621174	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529584	AAAAAAAAATTAGGC[C/T]GGGCTCTGTGTCTCA	3993
rs544682967	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75527369	CTTCTAATCAGAGTT[C/T]ACTCCTTTCCTCTGA	3993
rs544988647	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559519	TCTCTGCTGGGAATT[C/T]CATGGGGCTATAGCA	3993
rs545064793	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564688	GACAACGTAGGGAGA[A/C]CCTTGTCTCTACAAA	3993
rs545074696	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75531071	TGCTTGCTGGGTACA[C/T]CCTCCTCACCCTGCT	3993
rs545135745	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524936	GGGCCTGCGTCGGAG[A/G]GGATGGGACGTCGCA	3993
rs545159945	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75552857	CATGGGGCTCATGGC[G/T]ACCGTTCTGGGCAGC	3993
rs545205140	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544045	CCCAGGAGAATGAGC[C/T]GGAGTTGGCCTCGGA	3993
rs545225069	snp	A/G	0.000241867	0.0109943	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570130	GCCCTTCGTGTTGGT[A/G]CAGTGTCAGCCCCCG	3993
rs545259622	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575203	ATAAACACCTATTAC[C/G]TCTTGACTGGTCCAC	3993
rs545309858	snp	A/G	0.000113205	0.00752263	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574414	GTGGCTAGCCGCCCC[A/G]AGGGCCTCAGTGGGC	3993
rs545314933	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75554717	ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA	3993
rs545316132	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548838	TTGGGGTGGTATGTC[C/T]TGAGTTCCAACAGCA	3993
rs545431193	snp	A/G	0.000133742	0.00817638	intron-variant	LLGL2	GRCh38.p7	17:75572081	TGCCACACGGGCAGC[A/G]GCGGGTCTCCCTGGG	3993
rs545433623	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542538	CTTCCCCCAAGGATA[A/G]TCCAGAAATGGTTTC	3993
rs545498207	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75545579	GAGGATTTGGGATCC[C/T]GTCTGCCCTGCCCCT	3993
rs545620385	snp	A/G	8.6494e-05	0.00657568	intron-variant, synonymous-codon	LLGL2	GRCh38.p7	17:75570510	AGAGGTGAGGCCTGA[A/G]GTGAGGCTGCGGCCG	3993
rs545621523	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527431	CTGGACAGGGTTTCC[A/G]GGGTCCAGGGTCATT	3993
rs545705680	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75538622	GAAAGCTGCTGCTTG[C/T]GGGGGATTCCACAGG	3993
rs545725980	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75536011	GTGGATGGGAACCAG[C/T]CACAAGGCAGCAAGC	3993
rs545768368	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545673	CCAGGGGTTGTGAGC[A/G]AGGGAGTGAATAGTG	3993
rs545801525	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567389	GAATCTCTTGAACCC[A/G]GGAGGCAGAGGTTGC	3993
rs545839222	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565892	TGCTATATGCCAGGC[C/T]CTGTTCTAGAAACAG	3993
rs545847961	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539311	AGTGATCCTCCCACC[A/G]TAGCCTCCCAAAGTG	3993
rs545877572	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75550046	GATGTGGGCGGGGCC[A/G]GGTAGGCTGGATGCC	3993
rs545889529	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75537760	AGCCTCCTAGGACTC[A/G]GAGAATGGTCAGGAT	3993
rs545953608	snp	C/T	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75561465	CCCTGTCTCTCCTCA[C/T]AAAAAATAAAAATTA	3993
rs545990474	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75531662	AGGGCAGGAGACGGG[C/T]GTCCCCCAGCGGGGC	3993
rs546067648	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75560950	GATTCTCCTGCCTCA[C/G]CCTTCCGAGTAGCTG	3993
rs546085461	snp	G/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75549644	CACCCAGCCAGTATC[G/T]GGCAGAGTGGCCCGG	3993
rs546129437	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533399	AAGCTCCGCCTCCCA[A/G]GTTCACACCATTCTC	3993
rs546130806	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571566	GTCAGAGAGCCTTCC[A/G]GCCTCTCCCAGGAGG	3993
rs546145870	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75557632	GGGAGGGGTATGGAG[C/T]ACTCGAGTTCCAGGC	3993
rs546218262	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566415	CTGCGGTGCAGGCCA[C/T]GGGACTGGCAGGAGG	3993
rs546230591	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75529203	CTGACAGTCCTTTTC[G/T]TTTTTTTTCTTTGAG	3993
rs546234734	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551731	TTCCTGCTGGTGTGC[A/G]GAATTGTCGAGGCCA	3993
rs546234790	snp	C/G/T	0.000417564	0.0144434	intron-variant	LLGL2	GRCh38.p7	17:75558083	ATTGCACATGGGCCC[C/G/T]GAGGGCCTGGCACTC	3993
rs546284108	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75529050	AATCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA	3993
rs546333538	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575695	GTGCGTGGGGTTCTC[C/T]GGTGTCTGAGACAAC	3993
rs546373659	in-del	-/G	0.0146672	0.084371	intron-variant	LLGL2	GRCh38.p7	17:75546859	CAGCAGACAGGCGGA[-/G]GGCAGGTCCAGCGGA	3993
rs546438751	snp	C/T	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75543909	GGTCCCTTGGGGCCC[C/T]GGAGTCACAGGCCAT	3993
rs546450386	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546929	GGCTGTTGGTGTAGG[C/T]GAGGGTCAGGCCCCA	3993
rs546471976	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552343	AAAATACAAAAACTA[G/T]CTGGGCGTGGTGGTG	3993
rs546631647	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75539861	TGATCCACCCGCCTC[A/G]GCCTCCCAGAGTGCT	3993
rs546659991	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75549599	AGGGAGGGCCAGGCT[A/G]CCGCCACTGCCAGGA	3993
rs546822875	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533993	TGACATCTGGAAGCT[G/T]CTTGGGACAGCTGTT	3993
rs546856732	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546465	CGAATCGAAGGCCAC[A/G]TCTGGCTGGCGGCTG	3993
rs546987209	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75550896	TTTCCTCAGGACACT[A/G]GGCCCTGGGTTTCTA	3993
rs547049675	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543337	TCCACCTGTTTGGGC[C/T]GGGCCTAATCGATAC	3993
rs547052204	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550432	CAGGGAAGCTAAGCC[C/T]TACAAGGCTGGTAGG	3993
rs547182272	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560714	TAGTCTCGAACTCCC[A/G]ACCTCAGGTGATTGA	3993
rs547214013	snp	C/T	3.37781e-05	0.00410949	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573113	GCCCACTTCGGCAGT[C/T]GTCGAGCCGAGGACT	3993
rs547218440	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531707	GCCCTCCCCAGCCCT[G/T]GCTCCCTAGGAATTC	3993
rs547270567	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75553289	TTTGCAGGGCAGGCC[C/T]TGTTCCTAGCAAAGG	3993
rs547306377	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531459	ATGTTCTTTCTCCTG[G/T]GCCGGCTGCTTTGAG	3993
rs547325474	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75572721	ATCCCAGCTCTACTC[A/G]GGAGGCTGAGGCAGA	3993
rs547354424	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75570852	GTGGCTGGCATGGCT[C/G]TGGCCTGCCTTCCGA	3993
rs547381275	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569710	TGGAAGGCCGAGACA[A/G]GAGAATCACTTGAAC	3993
rs547439010	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562544	CATGCTGCCCTTCTC[C/T]CCTTGGTGACATGTC	3993
rs547477092	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75545751	TTTGGGCAAGGCAGG[C/T]AAGCTCAGAGCAGTT	3993
rs547494879	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569387	GACTGGGGACAGCAG[A/G]GACAGGAGCCAACCA	3993
rs547609269	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75571183	ATGCCGGGGGCTGCT[A/G]CCTGCCTGGCTGGTA	3993
rs547798970	snp	A/C	0.0494327	0.149241	intron-variant	LLGL2	GRCh38.p7	17:75558824	TCCTCCATCCACACC[A/C]CGCCTCCTCCATCCG	3993
rs547842281	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530355	AAATTTTTTTAAAAA[A/T]TTAGCTGGGCATCAG	3993
rs547859305	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549265	GAACCATGGGACCTC[A/G]GGAGGGAGGAAGTGC	3993
rs547866389	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534808	TCTTGACTGTTTGAG[C/T]TTGGGGCCACTCTGA	3993
rs547899583	snp	A/G	0.000146743	0.00856445	intron-variant	LLGL2	GRCh38.p7	17:75572104	TCCCTGGGACTCCCC[A/G]GGACATCCAGGAGGC	3993
rs547927888	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529952	TTTGCCGAGTCCTTG[C/T]TGTGTGACCCTAGTG	3993
rs547929087	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75539489	GCTCAAGTGATCCTC[C/T]CACCTTGGCCTCCCA	3993
rs547933282	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559174	ATGGGCTTGTTTTCC[A/G]AGGAGTCAGGGGACC	3993
rs547994467	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532926	CTACCTCAGTGTTTC[A/G]TGGGGTCAGTGATTG	3993
rs548058903	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553913	TCGACATGGTTGTTG[A/G]ATTGCAAACCCTCTA	3993
rs548080684	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557014	AGCCTGGGCAACAGA[A/G]TGAGACTCTGTCTCA	3993
rs548088045	snp	A/G	1.89163e-05	0.00307535	intron-variant	LLGL2	GRCh38.p7	17:75564311	GGCTGTTGAGGCTGT[A/G]CCAGGAGCCCCAGCC	3993
rs548187505	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530015	CAGATGAGAAGATGA[A/G]AAAGGTCACTAGCAC	3993
rs548208539	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561715	CACCTGAGATCAGGA[A/G]TTCGAGACCAGCTTG	3993
rs548269955	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526150	ACCGCGGGCAGAGAC[G/T]GAGTCCCCGGGCCCA	3993
rs548350469	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531462	TTCTTTCTCCTGGGC[C/T]GGCTGCTTTGAGCAG	3993
rs548368878	snp	A/G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75550511	CGGGGCAGGCCGGGC[A/G/T]CGGTGGCTTACACCT	3993
rs548517874	snp	C/T			upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524857	TCCTCTGGTGCGGGA[C/T]CTAAGAGTGAGAGAA	3993
rs548587490	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544291	CTGGGACACTGTGAT[C/T]CTCTTCCCCCGGGGA	3993
rs548666506	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552462	CCACTGCACTCCAGG[C/T]GTGACAGGCGTGACC	3993
rs548735994	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544690	CTGTTGGGAGAGGTG[A/G]GTCGTGGGGTGGAGG	3993
rs548853776	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542207	GCCACCTCCCAAGAA[C/T]GCGAAATCCTTCAAA	3993
rs548894321	snp	C/T	0.00287035	0.0377748	intron-variant, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574186	AGGGCCCAGGCGGGG[C/T]GCCCTGACCCGGCCT	3993
rs549032147	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75533732	GACTGACAGAAAGTA[A/T]AAGTAACTAATAAAT	3993
rs549190432	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574547	GGCTCTGCCAGAGGG[C/T]TCAGGGGAGCGCTGA	3993
rs549279291	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529111	CAGTGAGCCGAGATC[A/G]TGCGATTGCACTCCA	3993
rs549333555	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540602	GGGAGCGTGTCTGTG[C/T]GTGTCCCTGCCTCTT	3993
rs549372910	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546413	TCAGAGCCACTCCAT[C/G]CATAGAGTTGGTGTG	3993
rs549460526	snp	C/T			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551331	GCCCAGTGCAGTCAC[C/T]AGTACCATCCCGTTT	3993
rs549482178	snp	A/C	0.0115144	0.0749975	intron-variant	LLGL2	GRCh38.p7	17:75530145	GGCCTTTTGGAAGTG[A/C]CTGATGGGTTTAGGG	3993
rs549500035	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570879	CCGATGCAAGGATCA[A/G]CACTGAGCGAAGCAC	3993
rs549538450	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526694	GGCTCCAGGGACCCC[C/T]TGCTGGAGTTTGTAG	3993
rs549634893	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537399	CTTTACCCCTTAGGA[C/T]AAAATGATCCCAGGC	3993
rs549675309	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526282	CCCCTGCCATCTGGG[A/C]TGTGTCCCTGCCGGC	3993
rs549717164	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568792	GCCAATTGATGGTGG[C/T]ACCAGCCTGACCCCA	3993
rs549720511	snp	A/G	0.00123622	0.024831	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564401	ACGGGCCAGCTACGG[A/G]GACCGCCACTGCATC	3993
rs549850701	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75565325	CCAGGAGGGAGGGCC[C/T]TCTCCTAATGATGCT	3993
rs549880602	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563924	CAGGTCCCGTGTTGG[A/G]GTCTTGGACACCAGG	3993
rs549928822	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75544157	AGGACGGGCCTGTAC[A/G]CAGGAGGCGTGCAGT	3993
rs549944528	snp	C/T	0.000311971	0.0124855	intron-variant	LLGL2	GRCh38.p7	17:75559219	TCCCCTGCTGGGCAG[C/T]GGTCGGCTCACGGGC	3993
rs549953349	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566592	GACAACACAAGGGGC[A/G]TATCCGTGTTCCAGG	3993
rs549956705	snp	A/G	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75550507	GGGGCGGGGCAGGCC[A/G]GGCGCGGTGGCTTAC	3993
rs550111483	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532711	ATTACAGGCATGAGC[A/C]GCTGCGCCCAGCCCT	3993
rs550127723	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542208	CCACCTCCCAAGAAC[A/G]CGAAATCCTTCAAAC	3993
rs550198975	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562864	CATGAGCCACCACGC[C/T]CGGCCATCCACTGCG	3993
rs550199194	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536207	CATCTCAGAGGTGGC[A/G]CTCTGGCTAGGTGGC	3993
rs550226252	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524475	GTCTGTTCTCAGGGA[A/C]CATCTCGGCTGCCTC	3993
rs550402005	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533454	GGACTACAGGCGCCC[A/G]CCATGATGCCCAGCT	3993
rs550418566	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567972	AAAAAAAAAGACAAA[C/T]GGTTTAATCATCCAG	3993
rs550441753	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557583	GCCACCTCCAGCGGA[C/G]CCTGACCTCCCTCTT	3993
rs550506418	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546432	AGAGTTGGTGTGAGG[A/T]CTACATGAGTTCCTG	3993
rs550563258	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544725	TCCCTGACCTCCCCG[C/T]TGGGAGAGGTGGGTC	3993
rs550649974	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75527732	TCAGCCTCCCAAAGC[A/G]TTGGGATTACAGGTG	3993
rs550702045	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550282	CCCTGGGGCTGAGCC[C/T]AACCTCCTGTGCTCA	3993
rs550789999	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567490	AAAGAAAAACAAAAA[C/T]TAGCCAGGCGTGGTG	3993
rs550800171	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75536189	GGTTTTCCTGAGAAG[C/G]CTCATCTCAGAGGTG	3993
rs550822555	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538964	GTGGTACAGTCATAG[C/T]TCACAGCAGCCTCAA	3993
rs550852436	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549447	GGGCCTTCCCTGCCC[A/G]TGCCCACCCTCCTCT	3993
rs550885858	snp	G/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75539581	ATAGTCCTGACCTCT[G/T]TCAGAAATCATCCCA	3993
rs550915914	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549816	CAGGATGAAGGCCCC[A/G]CTGTCTCTGACAGCC	3993
rs550918411	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572614	AGCTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC	3993
rs550967709	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542906	GAGGAAGCATCTGCC[C/T]GGTGCCCTGGCCTGG	3993
rs551034190	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75555683	CATTGTTCCAAACTC[C/T]CCCTACTTTCCCCAC	3993
rs551059131	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547409	CTCACTGTGTAAGAC[A/T]CAGTGGACGCATTAC	3993
rs551142618	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572154	GATGGCTGGGACTCA[G/T]TCTTGTTTGCAGTTG	3993
rs551167332	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553196	ATTTTTCGCATAGCT[A/G]AACAGGGACCTGGGC	3993
rs551190533	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75533060	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	3993
rs551254411	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543309	CTACTGGACTTGGAG[A/G]GAGAGGCCCTGCTCC	3993
rs551320970	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530852	TCAGAAGTTTTTCAG[C/T]GAGGACCTTTTTCAG	3993
rs551323351	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553750	GATTAAGAAACTGAA[C/G]TAAAAACCTTCCTGA	3993
rs551360301	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547889	AGGTGAGGGGAGGAA[C/G]TGTAGGTGAATGAAG	3993
rs551601533	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75574741	GAGCCCCGGCCCCAC[G/T]CCCCTGGGTCCCACG	3993
rs551712210	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574574	CTGAGAGTGGAGGTC[C/T]CTGAGGCCATGACTC	3993
rs551785163	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529213	TTTTCTTTTTTTTTC[C/T]TTGAGACGAAGTCTC	3993
rs551786088	snp	C/G/T			intron-variant	LLGL2	GRCh38.p7	17:75554168	TTAGCTGGGCATGGT[C/G/T]GTGGGTGCCTGTAAT	3993
rs551799537	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523129	GGTCACAGTGAGCCA[A/G]GATCACGCCACTATA	3993
rs551844209	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546903	AGGGCTGGAGCCTGG[A/C]GCGGCACGTGGGCTG	3993
rs551896770	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541522	AGTTTCCCGGCCACC[C/T]GCTCTTCCCCAGCAA	3993
rs551933549	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542079	CAAGCCCTCGGTTCC[C/T]CTGCCCGAAGACACC	3993
rs551956222	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563682	ATGAGCTAGAGGGAT[A/C]TGTGCCTGTGGGGAC	3993
rs551978951	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544635	GTGGCCCAGGAATGC[C/T]GGCTGCTGCTGTGGG	3993
rs551997474	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75571353	GACCCATCACTTAGC[C/T]TTTCAGGGCCTCAGC	3993
rs552061424	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530343	GCGTCTCTACAAAAA[A/T]TTTTTTAAAAAATTA	3993
rs552065445	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569661	TATAAAAATTAGCCA[A/G]GCATTTGTGGCTCGT	3993
rs552187047	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75546782	AGGTCCAGCAGACAG[A/G]CGGAGGGCAGGTCCA	3993
rs552193874	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75527466	ATCCCCATTCTTCCT[C/T]GAGGCAAGGGAGTTT	3993
rs552194126	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560385	GTGGCCACACCAGTG[C/T]CCAGCCTCACCCTGT	3993
rs552198320	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554467	AAATTAAAAAGTAGC[C/T]GGGTGTGGCAGGTGT	3993
rs552212909	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529726	ATTAGCTGGGCGTGG[C/T]GGTGCGTGCCTGTAA	3993
rs552234002	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75532375	CCTGACTCAGGCTCC[C/G]GAGTAGCTGGGATTA	3993
rs552321332	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538693	AACGTGGCCAGGTCC[A/C]AGGAGAAAAGCGGTG	3993
rs552321486	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531892	GAGGCTGCTCTGGGC[A/G]TGGGGACGAGGAGGC	3993
rs552433183	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554990	AGGTCAGGAGATAGA[A/G]ACACGGTGAAACCTG	3993
rs552446966	snp	C/T	1.67108e-05	0.00289052	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556067	GAGCATGGCTTCCCG[C/T]ACCAGCCCAGCGCCC	3993
rs552473517	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565496	TCACACCCTGGATGC[A/T]GAGAGCAGGGCCCAG	3993
rs552513388	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551226	CCCAAGGTGATACTA[C/T]GGAACAATGCGAGCC	3993
rs552563865	snp	C/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524679	CTGTGTGCCTTTAAC[C/G]AGAGGGTGCCTGCTT	3993
rs552648297	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525323	CAGAGGAGCTGGCCC[G/T]GATCCGCCCCTCCCT	3993
rs552662612	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565336	GGCCCTCTCCTAATG[A/C]TGCTGGCCTGAAAGG	3993
rs552673408	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550692	CGGGAGACTCAGGTG[G/T]ATCACTTGAGCCCGG	3993
rs552705816	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75549030	CAGCTGGAGCTTATC[C/T]GGGGCAGGGGCACTG	3993
rs552741441	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546119	GCAGTAAAGAGGGAG[A/G]GGATGGGGAGGGGAG	3993
rs552916199	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562383	AACTTTGATGCCCTC[C/T]GGAGGTCTTATGCAC	3993
rs552929044	snp	A/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75539057	GACACCATGCCTGGC[A/T]AATCCTTTTTGTTTG	3993
rs552942596	in-del	-/TTTTT			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541742	TTTTTTTTTTTTTTT[-/TTTTT]GAGATACTGTTTTTG	3993
rs552945329	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567989	GTTTAATCATCCAGC[A/G]CACATTTATTGAGCA	3993
rs553063520	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75572506	GTCTCTACAAACAAA[C/T]GCAAAAAAATTAGTT	3993
rs553246693	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528695	GTGAGCCAAGATCAC[A/G]CCATTGCACTCCAGC	3993
rs553285359	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75561797	CATGGTTGTGGGTGC[C/T]TGTAATCCCTGATAC	3993
rs553391050	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530426	GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG	3993
rs553397910	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567563	AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG	3993
rs553415717	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535104	CGACATGGGCACTTG[C/G]AAAGCGGCTACAGGC	3993
rs553449250	in-del	-/A	0.331179	0.236453	intron-variant	LLGL2	GRCh38.p7	17:75527168	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs553456248	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541804	GCCTGATCTTGGCTC[A/G/T]CTGCAACCTCCGCCT	3993
rs553516660	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75564092	GTTTCTTCAGACAAA[A/G]TCACTCTGGGTGATG	3993
rs553593401	snp	A/G	0.02016	0.0983543	intron-variant	LLGL2	GRCh38.p7	17:75533235	TGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTC	3993
rs553601201	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567063	ACAGCTGAGCCCGGG[C/T]ACCCTCAAGCCTTGG	3993
rs553639541	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561487	TAAAAATTAGTTGGG[C/G]AAGGCGGCACACGTC	3993
rs553663522	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524696	GAGGGTGCCTGCTTC[A/G]TGCTATAAAGCCAAA	3993
rs553734536	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524111	ACCAGTGCTCTGGGG[C/T]GCTCTTCATCAGAGC	3993
rs553795052	snp	A/G	1.73495e-05	0.00294524	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570036	CCGACCTGCTGCAGG[A/G]CCAAGAGGGCTACCG	3993
rs553870961	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573780	CTCCTTGCCTCTTTG[C/T]GTGCCCCTTGCCCCT	3993
rs553929286	snp	A/C/G	0.000204892	0.0101196	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559393	CCGGACCATCAGCTC[A/C/G]GACGCGGTGCTGCAG	3993
rs553945932	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75568906	GGAGCAGAGCCCTGA[A/G]GTGGACGAGCCAGCC	3993
rs553982764	snp	G/T	1.68131e-05	0.00289935	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563153	TACAGGGCAGCCGCG[G/T]GCTCTACCACTTCCT	3993
rs554033634	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547130	TCAACTCCTTTATAC[C/T]CACACCAAGCCCGAT	3993
rs554168180	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523173	GACAGAGTGAGACTC[C/T]GTTTAAAAAAAAAAG	3993
rs554179977	snp	A/G			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525163	GCAGACCCTCCGGCC[A/G]ACACGGAGGAGGTGG	3993
rs554242536	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552053	AGAATCATTTGAACC[C/T]GGGAGGTGGAGGTTG	3993
rs554267763	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75534733	GGATTCTCCTGCCTC[A/G]ACCTCCCAAAGTGCT	3993
rs554302821	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75555660	TTCTCCCGAGAGACC[C/G]GTGTCTCCATTGTTC	3993
rs554308067	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555904	AATATGGGTTAGGCT[C/T]CAACACTCAGGTGTC	3993
rs554475289	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75537733	AACCATGGTGGACAG[G/T]GACAGCCTCCCAGCC	3993
rs554501614	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555329	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGCTCTGC	3993
rs554505044	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548710	GCAGTGAGCCAAGAT[C/T]GCGCCATTGCACTCC	3993
rs554528235	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75552752	TGTTCTTCTAGAACC[C/T]GAGTTGTTCCAGACA	3993
rs554643389	snp	C/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75549539	GTTGTTCTGTATTGG[C/G]TTTCGAATGGCTGGG	3993
rs554655727	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526365	TCTCCGGCCTTTCTC[A/C]AGCTGGGGCGGCTTT	3993
rs554666503	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554497	TGGTGGTGCATGCCT[C/G]TAGTCCCAGCTACTT	3993
rs554733828	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571471	ACGTGTCTCTCCCTG[C/G]CTGGTTCTCCCCTGC	3993
rs554768067	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544901	TTGGGCCTTGGGATA[C/T]GGGGGTGCAGGTGTT	3993
rs554794891	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545255	CACTCCCAGGCCTGG[A/G]GGTGGCAGAGGGAGG	3993
rs555021809	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75546133	GGGGATGGGGAGGGG[A/G]GGCGGGTGTGCAGGA	3993
rs555209743	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575027	GCTGCTCTGGGCCTC[A/G]GGAGAGGAGAGACCC	3993
rs555242701	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531972	TTCTCTCGAGACACC[C/T]GACTTAGTGTTCCCA	3993
rs555307724	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540896	AGGACATTCAGCGAC[C/T]CATGACTGTGACTCT	3993
rs555333873	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530409	TAATTCCAGCACTTT[A/G]GGAGGCCGAGGCAGG	3993
rs555335273	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534406	GCGAGCAGGCAGCCC[C/T]TTTGTCCTGGGAGAG	3993
rs555418299	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551819	ATAATTATTTAAACA[C/T]GTGAAATTAATTTTA	3993
rs555451854	snp	C/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75533234	TTGATCTCCTGACCT[C/G]GTGATCTGCCCGCCT	3993
rs555468396	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75549743	CCCACCCCCTGAGGA[A/G]TGCCAGGGACTCCTC	3993
rs555592535	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528515	AGGCCAAGTTGGGCC[A/G]ATCGCCTGAGGTCAG	3993
rs555658882	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75534959	ACAGTCCTCCAGTCA[C/T]GCCCCCATTCCCTCT	3993
rs555724187	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75529476	TCTCAAAGTGCTGGG[A/G]TTACAGGCATGAGCC	3993
rs555776887	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524823	TCACCCCTGCTTTGC[C/T]CACTCAAGGAGATCC	3993
rs555791534	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567636	AGAGCAAGACTCCAT[C/T]TCAAAAAAAAAAGAG	3993
rs555792229	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532610	TGTATTTTTAGTAGC[A/G]GGGGGGTTTCCACCA	3993
rs555840385	snp	C/G			intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523414	TGGCTCCTGAAGTAG[C/G]GTGTAAACTAGAGGA	3993
rs555910959	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542011	GCTGGGATTACAAGA[C/G]TGCCATTTTTTACAG	3993
rs556036509	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525480	TGCGTCCAGGTGCGC[G/T]CAGGTGAGGCCGGGG	3993
rs556037980	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75556366	GGGATGCGACCCTGT[C/T]CTTTGCAGGAGGACA	3993
rs556112102	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542871	GAGAGTCCCTGGACA[A/G]CCTTCCCCGAGGTCA	3993
rs556150800	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75561169	GTCCTCTTGATGACA[C/T]TTATCTAAGTTTTTA	3993
rs556185931	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564679	TCCAGCCTGGACAAC[A/G]TAGGGAGACCCTTGT	3993
rs556198703	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75559534	CCATGGGGCTATAGC[A/T]GGGGAGGCTCTTGGC	3993
rs556220892	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565506	GATGCTGAGAGCAGG[A/G]CCCAGCTCTGCTCTT	3993
rs556247255	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531010	TGGTGGGGATGTCGG[A/C]GAGTGCAGGATTAAA	3993
rs556280104	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554675	CTTTGGGAGGCCAAG[A/G]TGGGCGGATCGAGAC	3993
rs556401189	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75558336	GGCATTCGGTGGCCC[C/T]GGGTTTGCTGCTGAT	3993
rs556457448	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574379	CATGGGCACCCACGG[A/G]GAAAGGGGGTGGAAG	3993
rs556472240	snp	C/T	0.263535	0.249633	intron-variant	LLGL2	GRCh38.p7	17:75558845	CCTCCATCCGCACCC[C/T]ACCTCCTCCATCCGC	3993
rs556526961	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75535935	AGGAAACAGGTCGAT[C/T]AGCTGCCCACAGGGA	3993
rs556560094	snp	C/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75553366	GCATCCCCCAAAATA[C/G]GCACTTGTTGGAGCT	3993
rs556637068	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556201	GTGGGTGAGATTTGG[A/G]GAGGGACATCTTTTC	3993
rs556724886	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550677	GTAGTTCTAGCTACT[C/T]GGGAGACTCAGGTGG	3993
rs556760950	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543153	AATGGCTTCCTCCCC[C/T]AGCTTTTCCTACCCC	3993
rs556824279	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535491	GAACTTCCCGAGCTA[A/T]GGAGGGAGTTTCTTG	3993
rs556903008	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544351	GGACATGTGGCTTTC[A/G]TTGGGGGCTTCCGTT	3993
rs556919693	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75537675	GCACTTCAGCCTGGG[C/T]GACAGAGCGAGACTC	3993
rs557015408	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544011	TTCTGGCTCCGGCCG[C/G]GGTGAGTGGGGAGAG	3993
rs557038687	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75545056	CTGCCTCCAGTCTTT[C/T]GCTTTGAAAAGGTGG	3993
rs557048191	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566306	ATCTAGCCTCTGCTC[C/T]AGAAGGATCTGTCTG	3993
rs557103058	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572401	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	3993
rs557123613	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566946	CAGAGATGTGTGAAG[A/G]CTGCTCAATGATTTT	3993
rs557153688	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75549366	CCCAGGCACACCCCA[A/G]GCAGCCACACCCATC	3993
rs557160744	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561271	TCATTGTAGGGCTGT[G/T]TTTAATGGCAAAAAG	3993
rs557164318	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533305	CACCTGGCCCTTTTT[C/T]TTTTTTTTTTTTTTT	3993
rs557186063	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545563	ATGAGGCCAGATCCC[A/G]GAGGATTTGGGATCC	3993
rs557197827	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540703	TGACTTGGGGTCCAG[C/T]CCGAGTTCTGCCGCT	3993
rs557223100	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575153	CTGGGTTTTAAGTTA[C/T]AAATGTTAACTGCCT	3993
rs557273539	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545491	AGGGGATTCAGGAGC[A/G]GGGTAGACTCATCCG	3993
rs557309090	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75526960	ATCGCCTGAGCCCAG[A/G]AGTTTGAGACCAGCC	3993
rs557372629	snp	C/T	1.77146e-05	0.00297607	intron-variant	LLGL2	GRCh38.p7	17:75571848	GTCCAGGGAGTGGCT[C/T]CAGCCCTGCCACCCC	3993
rs557392577	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532455	TTGAGTCTGAGTCTC[A/G]CTCTGTCGCCCAGGC	3993
rs557441352	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557839	ACCAAGCGACAGCCA[A/G]CATGTCTTTTGCAGC	3993
rs557563366	snp	C/T	0.130351	0.219509	intron-variant	LLGL2	GRCh38.p7	17:75558865	CCTCCATCCGCACCC[C/T]GCCTCCTCCATCCGC	3993
rs557590959	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75532068	TATACACACACACAC[A/C]CACACACACTTTTTT	3993
rs557605436	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571545	TATGTTGGGGCCTGT[A/G]TGGTTGTCAGAGAGC	3993
rs557654412	snp	A/T	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75526489	CTATCTTGCCAAAGA[A/T]AGTGTGTCTTAGTTT	3993
rs557725664	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530199	CTGACGGCTCATGAA[G/T]TTGTGATATTTTAAA	3993
rs557771452	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573735	GAGGCACCTCCCCAC[A/G]AGCTCAGCCCACCCT	3993
rs557854333	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75534437	AGGCCTGACCTGAGC[A/G]GAGGATTCTGCAGTC	3993
rs557880450	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573382	TGGATGGGCCTTAAG[C/T]GGAGAACTGCGAGGG	3993
rs557966742	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524023	CTAGGACTCACCCAG[C/G]AGAAGGGATGTGGAT	3993
rs557980233	snp	C/T	2.00226e-05	0.003164	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568441	TGGGCTGCTTCCTCC[C/T]GGCCCCGGCCCCTGA	3993
rs558044972	snp	C/T	7.28491e-05	0.00603484	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569986	ACTGGAACTGAATGA[C/T]GAGGCAGCGGAGCAG	3993
rs558051384	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75530400	TCACGCCTGTAATTC[C/T]AGCACTTTGGGAGGC	3993
rs558112313	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546568	GCCCAGCAGACAGGC[A/G]GAGGGCAGGTCCAGC	3993
rs558142740	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75551578	GCCCAACCCTTTGTC[C/T]TCCTCTGAGTTAGAG	3993
rs558180823	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75562725	AGCCATGTGCCACCA[C/T]GCCCAGCTAATGTTT	3993
rs558302190	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526322	CTCCTAATCCCCGGA[C/T]GCAGGAAGCCCGCGG	3993
rs558308426	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75561718	CTGAGATCAGGAGTT[C/T]GAGACCAGCTTGGGC	3993
rs558338878	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564702	ACCCTTGTCTCTACA[A/G]AAAATAAAAAAATTA	3993
rs558372625	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552642	TCAGTTCAGACATTA[A/G]ATCTTTTTTGGAAGT	3993
rs558403128	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532269	TTTTTTGTTTGTTTT[C/G]AGACGGAGACTTGCT	3993
rs558482455	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536404	GGACGATGGAATAGA[A/G]AAGTCCTTTCTACTC	3993
rs558483014	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554025	AGTCATTTTAGGCCG[A/G]GTATGATGGCTCACA	3993
rs558508744	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75557832	AGGTGCTACCAAGCG[A/G]CAGCCAACATGTCTT	3993
rs558585967	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559955	GGTGGGAGAAGGGGA[C/T]GGGGCCCAAAAAAAG	3993
rs558617912	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560643	AGGCATGCGCTACCA[C/T]ACCCAGCTAATTTTG	3993
rs558640658	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75531571	CAGGGTTCCTCCTGG[A/G]GCGAGGCACGCCAGG	3993
rs558678051	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549437	GCACCTGCCTGGGCC[A/T]TCCCTGCCCGTGCCC	3993
rs558763545	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544432	TGGAAAAGGGATGTC[G/T]CCCTGTGGAGAATGA	3993
rs558781494	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75561378	GACACAGTTGCTCAC[A/G]CTTTGGGAGGCTGAG	3993
rs558820385	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75559802	TGCGGTGGGTACTTT[A/G]CTGAGGTTCCATTTG	3993
rs558866727	snp	A/G	0.000105915	0.00727643	intron-variant	LLGL2	GRCh38.p7	17:75570516	GAGGCCTGAGGTGAG[A/G]CTGCGGCCGGCCACG	3993
rs558900017	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543105	TTAACCTCAGGGCCC[A/G]CCGGCCCTCCTTGTG	3993
rs558953898	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548206	AGATGAGGGATATTC[C/T]GCCTGTACTTGACTA	3993
rs559074977	snp	G/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75539377	TTCTTTTCAAAATTT[G/T]TATTGTTCCATGTAA	3993
rs559232777	snp	C/G			synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574223	TCCAGAGAAGCAGCC[C/G]GGCCTGGTGATGGAG	3993
rs559239139	snp	C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537453	AATCCTAGCACTTTG[C/T]GGGGCCGAGGTGGGC	3993
rs559341760	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567434	ATGCCATTGCACTCC[A/G]GCCTGGGCAACAAGA	3993
rs559348478	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75547786	GCCGAGATCATGCCA[C/T]TGCACTCTAGCCTGG	3993
rs559388434	snp	A/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75531664	GGCAGGAGACGGGCG[A/T]CCCCCAGCGGGGCCA	3993
rs559392601	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567882	GGAGGTGGAGGTTGC[A/C]ATGAGCCGAGATCAC	3993
rs559477864	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75562300	CAAAAATGCACTGAA[A/T]ATGAATGTACAGTTT	3993
rs559531575	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75526552	CCTTGGCTGTGGGGA[G/T]AACTGACCTAACCAG	3993
rs559564625	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567356	GTAATCCCAGCTACT[C/T]GAGAGGCTGAGGCAG	3993
rs559565160	snp	A/C	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75528272	AGGCGCCTGCCATCA[A/C]GCCCGGCTAATTTTT	3993
rs559591851	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554994	CAGGAGATAGAGACA[C/T]GGTGAAACCTGTCTC	3993
rs559630100	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555570	GGAGGGACCTGGAAG[A/G]GCCCAGAGCAGGGCA	3993
rs559640357	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75544053	AATGAGCCGGAGTTG[C/G]CCTCGGACTACCCCA	3993
rs559679726	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526033	CGGGAAACTTCTCTG[A/C]CTGATCTGCGCGATG	3993
rs559747793	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75538411	TCTCATCTTGAGGCT[C/T]TGCAGCTGTTGTTCC	3993
rs559778657	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529732	TGGGCGTGGTGGTGC[A/G]TGCCTGTAATCCCAG	3993
rs559843811	snp	C/T	7.36092e-05	0.00606623	intron-variant	LLGL2	GRCh38.p7	17:75571151	AGTGGGCAGCAGACA[C/T]CCCCTGACCTGGGGG	3993
rs559844866	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75565949	AGATCTGAGTATGTG[A/G]ACAGAGTGAGTAGGT	3993
rs559932405	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75571590	CAGGAGGGAAAACCT[A/G]GGAGTAAACCCTGGT	3993
rs559932866	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544636	TGGCCCAGGAATGCT[A/G]GCTGCTGCTGTGGGC	3993
rs560031747	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75552989	CTGCTGGGAAAGTGC[C/T]GCTGTCCTGGGAGAC	3993
rs560032005	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536452	GGTTGCACAGCTAGT[C/T]CCACCTGCCTGTCTC	3993
rs560292745	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569551	CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGA	3993
rs560344367	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75543800	TCATGGGAATAAAAC[A/G]ATCTGCCATGTCTAC	3993
rs560412095	in-del	-/CACCGGCCTGACTGGGAAAAATCTCCCAGGGATCAGGT	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75557920	CTATGGAGTTGCTCC[lengthTooLong]CACTGGCCTGGTGCC	3993
rs560606336	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562751	TGTTTTATATTTTTA[A/G]TAGAGACAGGGTTTT	3993
rs560657211	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75547034	AGCTGGGACAGTGGC[A/G]CCATCACAGCTCGAC	3993
rs560664239	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75528285	CACGCCCGGCTAATT[G/T]TTTGTATTTTTAGTA	3993
rs560700780	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542413	CCTGCTGGGAGTGGA[C/T]GGAGCTGTGCCCAGG	3993
rs560734517	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531748	CTCGCTCACTGTGCC[C/T]GTGGCCATGGCTTTG	3993
rs560808617	snp	A/G	1.6836e-05	0.00290133	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573122	GGCAGTCGTCGAGCC[A/G]AGGACTACGGGGAGC	3993
rs560819119	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75548907	GTGCCTGACACAGGT[C/T]GACGCCTTACCAGGA	3993
rs560833543	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554883	GACAGCGCAAGACTC[C/T]GTCTCAAAAAAAAAA	3993
rs560865340	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75546591	GGTCCAGCAGACAGG[C/T]GGAGGGCAGGTCCAG	3993
rs560913206	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75538535	TCATTCAACAGATAA[C/T]GAGTGAGGACTCGCT	3993
rs560923189	snp	A/G	0.000137478	0.00828975	intron-variant	LLGL2	GRCh38.p7	17:75570279	GGGCGGCTGGGTCCC[A/G]GGGCTGGGAGTGGGG	3993
rs560977991	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544106	ACCAGAAGGCCCACG[A/G]GGCTTCCCTTCAGGA	3993
rs561039690	snp	C/T	6.87545e-05	0.00586281	intron-variant	LLGL2	GRCh38.p7	17:75571661	CCAAACATGGCTTCT[C/T]GGCAGGCTCCCGGCA	3993
rs561126369	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536702	AGAAAAAAGAATCAC[C/T]ACTAATCCCATAACC	3993
rs561207669	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571201	TGCCTGGCTGGTAGG[A/G]GCTAAGAGGTTTCCC	3993
rs561208905	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537976	CACCATACCTGGCTA[A/T]TTTTTTGTCTTTTTA	3993
rs561215191	snp	A/G	0.000130455	0.00807529	intron-variant	LLGL2	GRCh38.p7	17:75570531	GCTGCGGCCGGCCAC[A/G]CACCCAGGTTCGGCT	3993
rs561218131	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75541037	GTACACTCACTCCCT[A/G]CTGCACAGCAGGTGC	3993
rs561238931	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549172	TATATATGGTGGGCC[A/G]TCAAGCCTATTGGAG	3993
rs561290302	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75559995	AGCATCTGACAAGAT[C/G]ATGTTGGGGCCGGGT	3993
rs561315377	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530664	CAAAAAAAAAAAAAA[A/G]AATTAGCTGGGCATC	3993
rs561349605	snp	C/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75560002	GACAAGATCATGTTG[C/G]GGCCGGGTCGGTCAT	3993
rs561482788	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75564124	TCAAACAGAATTGGT[A/G]GGGGCACCCAGCATG	3993
rs561492115	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554381	CTTTGGGAGGCCGAG[G/T]CAGGAGGATCGCTTG	3993
rs561512908	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533442	CCTGAGTAGCTGGGA[C/G]TACAGGCGCCCGCCA	3993
rs561633172	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564824	AACCAGGATCATGCT[A/G]CTGTACTCAGCCTGG	3993
rs561650224	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562819	AAGTGGCCTGCCCAC[A/C]TTGGGCTCCCAAAGT	3993
rs561654185	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75532861	GGCCCTGGCCTTGGC[C/G]GGAGACTTGAGGACA	3993
rs561699946	snp	C/T	1.78819e-05	0.00299009	intron-variant	LLGL2	GRCh38.p7	17:75573001	GGCATGAACAACCAC[C/T]CCACGCCCCCAGGTG	3993
rs561715260	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528320	TGGGGTTTCACTGTG[C/T]TAGCCAAGATGGTCT	3993
rs561762568	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551603	TTAGAGGAAAGATGC[G/T]GAGCCGAACAGGAGT	3993
rs561771288	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533684	AAAGATGTCTGCCGT[C/T]GTTGAAAGTTGTTTC	3993
rs561807019	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526609	CTCTCACCTGAACAG[A/G]TGAGCTTTGAGTGAG	3993
rs561897581	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550731	GGTTACAGTGAGCTG[A/G]GATCGTACCACTGCA	3993
rs561899828	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75545145	CACCAAGTTCTGTCT[A/G]TGCAGCTGAGTGAGG	3993
rs561919125	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75559598	CTGTCATAGGTTAGC[A/G]TCATAGCACTAAAAA	3993
rs561924483	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75528829	AGGAGCCCATAGTGG[A/G]AAAAAGGAAACATTG	3993
rs561970562	snp	C/T	6.89168e-05	0.00586972	intron-variant	LLGL2	GRCh38.p7	17:75555999	GCAGCCATGGTGGCG[C/T]GAAGGGGACAGGTCT	3993
rs562128101	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566550	AGCTACTCAGCCTAA[C/T]GCCATTGCAGAGCAC	3993
rs562217011	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561019	GTATTTTTAGTAGAG[A/T]CGGGGTTTCACCATG	3993
rs562258020	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75547418	TAAGACACAGTGGAC[A/G]CATTACTTAGCCTCT	3993
rs562267406	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524188	AACTCCTTCCGTAGA[A/C]TCTCTTCTCTGGGAG	3993
rs562297730	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543286	TGGCCTGGCCCCGGG[C/G]TGGCAGCCTACTGGA	3993
rs562460411	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75547744	GCAAGAGAATCAGTT[A/G]AACCCTGGAGGCGGA	3993
rs562500462	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75548300	TTTTTTTTTTTGGAC[A/G]GAGTTTAGCTCTTGT	3993
rs562541388	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75538826	ACAGGCTCTGACAAG[A/G]GAATGGTCACTGAGA	3993
rs562549152	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536286	CTCAGCCTGTGGGCT[C/T]CTGAACTTGTCTCTT	3993
rs562563547	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574553	GCCAGAGGGCTCAGG[A/G]GAGCGCTGAGAGTGG	3993
rs562591562	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541594	AGGCAGGAACATCCC[A/G]GAATGACCCCCTTTT	3993
rs562852726	snp	G/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543404	TTCTCCAGGTCTCCA[G/T]TGGGGGCTGCAGACT	3993
rs562923810	snp	G/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75529880	AATAATAATAATAAT[G/T]TTTAAAAAAAGATTT	3993
rs563056359	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526726	TCAAGAGAACCTTGA[A/G]TTCTCTTGAAGGGGC	3993
rs563059365	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75569590	GGCGGATCACCTGAG[A/G]TCAGGAGTTCGAGAC	3993
rs563073227	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551838	AAATTAATTTTAATT[A/G]TATATTCTGGCTGGG	3993
rs563082132	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535225	GGGCGGATTCACATC[C/T]GTCAAACAGGAGGCC	3993
rs563142970	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530327	GGGCAACAGTGAGAT[C/T]GCGTCTCTACAAAAA	3993
rs563154431	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542521	CACAGAGGCTCCTTC[A/C]CCTTCCCCCAAGGAT	3993
rs563230012	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75544588	CTTGTTAAGGGCGTA[C/T]GTGGGGTGAGGTAAC	3993
rs563263151	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75550781	TGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAA	3993
rs563320184	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532763	TAATATAATTCTGGA[A/G]TTCTCTGGGGGTCCT	3993
rs563481975	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526702	GGACCCCCTGCTGGA[G/T]TTTGTAGTTCAAGAG	3993
rs563569358	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75532314	GGAGTACAGTGGCGC[A/G]ATCTCAGCCCACTGC	3993
rs563613304	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565828	TGGTTCTGCTGTGCC[A/G]GGTTGTGACCCAGCT	3993
rs563649082	in-del	-/CTCCAGCCCTGCCACCCC	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75571846	GGGTCCAGGGAGTGG[-/CTCCAGCCCTGCCACCCC]CTCACCAGCCCCAAC	3993
rs563683783	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75531298	ACTGTGGGAGATCTG[C/T]GCATCTCTGGCAAGA	3993
rs563700137	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75543799	ATCATGGGAATAAAA[C/T]GATCTGCCATGTCTA	3993
rs563717229	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525189	GGTGGGCGCCCCCCC[A/G]CACCCCCCCCCGAGG	3993
rs563720025	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562908	CATATTTCTATGCTG[G/T]CACATGGAGCAGCCA	3993
rs563738703	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561815	TAATCCCTGATACTC[A/G]GGAGGCTGAGCAGGG	3993
rs563763065	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75574730	GCTGGGAGGAAGAGC[C/T]CCGGCCCCACTCCCC	3993
rs563773363	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536976	GGGGTTACAGGCACC[C/T]ACCACCATGCCCGGC	3993
rs563786230	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75525980	CCTGTCCGCGTCGCT[C/G]TGCTGGCCTGGAAGA	3993
rs563789249	in-del	-/A	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75532933	GTGTTTCGTGGGGTC[-/A]AGTGATTGGCAGATA	3993
rs563807184	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533798	GAACTAGAGCAACAA[C/T]TGGGAACCCGCATGG	3993
rs563853032	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570737	CCAGTAAACGTTAGT[G/T]ATTTCCTTTTTCTCT	3993
rs563907128	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75528915	TGTAATCCCAACACT[G/T]TGGGAGGCGGAAGCA	3993
rs563921672	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536318	TCCACATTCCTCCCA[A/G]GTGTGTCACTTAAGT	3993
rs563930463	snp	A/G			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573236	ATCCGCCGGGAGGAC[A/G]TCAGTGGCATCGCCT	3993
rs563954111	in-del	-/TT			intron-variant	LLGL2	GRCh38.p7	17:75537809	TTTTGGAAGGTGACC[-/TT]TTTTTTTTTTTTTTT	3993
rs564014557	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563273	ATGGGGTGCAGGCGA[C/T]GGGAACGCCGCCTCG	3993
rs564047128	snp	A/G	5.39418e-05	0.00519307	intron-variant	LLGL2	GRCh38.p7	17:75558038	GTCCTGCTGCCTCGG[A/G]GGAGGGCAGCCCCTC	3993
rs564059758	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75550830	CAAACTAGGGGGCAA[C/G]TGGGGCACAGCCAGA	3993
rs564081275	in-del	-/AGGAGAGC	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526089	CAATAATGTTGGCTT[-/AGGAGAGC]AGGAGAACAGGTGCC	3993
rs564122278	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552317	AACTTGGTGAAACCC[C/T]GTCTCTACTAAAAAT	3993
rs564142434	snp	A/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75533223	CCAGGATGGTCTTGA[A/T]CTCCTGACCTCGTGA	3993
rs564332125	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540340	CCCTCTTCAAGGAAG[C/T]GTGGTGCTTTTCCAT	3993
rs564338421	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75552905	CTCCTGGCCAGGCCA[C/T]TGGGCTCCTGTAGGG	3993
rs564346215	snp	A/G	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75533467	CCGCCATGATGCCCA[A/G]CTAATTTTTTGTATT	3993
rs564468961	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75556414	CTGAGGAGATACAGG[C/T]TTATTTTGTCTCCTG	3993
rs564502153	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75550365	GGAACTGTTCCTGAA[C/T]CCTAAACAAGGGGGG	3993
rs564562894	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75555176	GCGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAT	3993
rs564582424	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75562001	CTAATGTCAGTGAGG[G/T]CAGTGCTAGCAGTAG	3993
rs564724783	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572625	AGCCGAGATTGTGCC[A/G]CTGCCCTCCAGCCTG	3993
rs564729330	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75537119	TGAGCCACAGCGCCC[A/G]GCCCTTTTATTCCTT	3993
rs564741180	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537803	GAAGGCTTTTTGGAA[G/T]GTGACCTTTTTTTTT	3993
rs564910569	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570823	AAGGGTCCCTCTAGA[C/T]GCAGGCCTGGCAGGT	3993
rs564931216	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548321	TAGCTCTTGTTGCCC[A/G]GGCTGGAGTGCAATG	3993
rs564948094	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75559155	GACCTCATTAAAGGG[C/T]CTTATGGGCTTGTTT	3993
rs564958338	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75574033	ACACCCGGCCCAGAC[C/G]TGGGGCTGGACGGGA	3993
rs565053540	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548848	ATGTCCTGAGTTCCA[A/G]CAGCATCATAATGAT	3993
rs565165547	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569578	GAGACCAAGGCAGGC[A/G]GATCACCTGAGGTCA	3993
rs565197192	snp	C/T	0.00028581	0.0119509	synonymous-codon, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574493	ACTGGAGGGAGACCG[C/T]GGGTGAGGCACCGCC	3993
rs565283738	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535464	TCTCCCAGCAGATCA[A/G]TGAGATCAATGGAAC	3993
rs565392763	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571363	TTAGCCTTTCAGGGC[C/G]TCAGCTTGCTTCTCT	3993
rs565398507	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569664	AAAAATTAGCCAGGC[A/C]TTTGTGGCTCGTGCC	3993
rs565399721	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547174	CAAGGACATCGCCCC[A/G]GGGGTCCTGAGAGGG	3993
rs565452606	in-del	-/T	0.201727	0.245295	intron-variant	LLGL2	GRCh38.p7	17:75537810	TTTTGGAAGGTGACC[-/T]TTTTTTTTTTTTTTT	3993
rs565458097	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530605	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	3993
rs565515125	snp	C/T	3.295e-05	0.00405881	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524295	AGACCTCTGCAGCCT[C/T]AAGCGGTTGTCTTAC	3993
rs565519650	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566731	GGATGACGTGAGGGT[G/T]TGCTGGGAGCACCAG	3993
rs565525209	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75533450	GCTGGGACTACAGGC[A/G]CCCGCCATGATGCCC	3993
rs565546095	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536087	AGAGCAGGGCAGAAC[A/G]GGGAGGGTGGCTCAG	3993
rs565612856	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75554037	CCGGGTATGATGGCT[A/C]ACACCTGTAATCCCA	3993
rs565626525	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528642	ACTCAGGAGGCTGAA[A/G]CAGGAGAATCGCTTG	3993
rs565653996	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75529775	CTGAGGCAGGAGAAT[C/T]GCTGGAACCCAGGAG	3993
rs565667408	snp	A/C	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75532395	AGCTGGGATTACAGG[A/C]GCCCGCCACCACGCC	3993
rs565678374	in-del	-/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75559046	ATGCTGGAGGGTCCC[-/T]GGCGTCTTTCCTGCC	3993
rs565800181	snp	A/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561207	CAACCCTTTAGTCTC[A/T]TAACTGTCTCTGAGA	3993
rs565805731	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531909	GGGGACGAGGAGGCT[A/G]CAAGGCACCTGACTC	3993
rs565805959	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538752	ATTGCAGCTTCAGGT[C/T]GGGGAGGGCGTGAAG	3993
rs565893403	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544843	ACATTTGCCTCTGGA[A/C]TTAGGGCTTTCCTAT	3993
rs565967475	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75561674	GCCTGTGATCCCAGC[A/G]CTTTGGGAGGCGGAG	3993
rs565997065	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75550608	TGGGCAACATAGTGA[C/T]ACCTCATCTCTACAA	3993
rs566003699	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525327	GGAGCTGGCCCGGAT[C/T]CGCCCCTCCCTCGGC	3993
rs566061629	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575007	ATCCCGGCTTCCACA[A/G]TGCAGCTGCTCTGGG	3993
rs566141567	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544273	GAAGGTGGGCTGCAG[A/G]AACTGGGACACTGTG	3993
rs566228260	snp	C/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537454	ATCCTAGCACTTTGT[C/G]GGGCCGAGGTGGGCA	3993
rs566254974	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75549169	TGCTATATATGGTGG[G/T]CCGTCAAGCCTATTG	3993
rs566368007	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531891	AGAGGCTGCTCTGGG[C/T]GTGGGGACGAGGAGG	3993
rs566370055	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75551153	TGTGAAGGTCACTGC[A/C]CTTATTTTGGTTTTA	3993
rs566445334	snp	C/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75547012	CCAGTCTGCTGGGTA[C/G]TGTGACAGCTGGGAC	3993
rs566538873	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533216	GTGTTAGCCAGGATG[A/G]TCTTGATCTCCTGAC	3993
rs566562559	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75557683	GCCAGGGCCTTGCTG[C/T]GGGCTCAGCCTTCCC	3993
rs566667433	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541633	CCCAGAAGGTGACAG[C/G]GCTCTGGGGGCTGGT	3993
rs566670029	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75534846	ACTTCATAAGTAATT[A/G]TAAGAATTAAATAAG	3993
rs566724874	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529056	AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAATCG	3993
rs566751216	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539873	CTCGGCCTCCCAGAG[C/T]GCTGGGATTACAGGT	3993
rs566780078	in-del	-/A	0.451856	0.147493	intron-variant	LLGL2	GRCh38.p7	17:75554888	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs566798866	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533534	TGGTCTCGATCTCCT[G/T]ACCTCATGATCTGCC	3993
rs566808472	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75545851	ATGGGAACGAGGCAT[A/G]AATTGAGCAGGGTTT	3993
rs566863654	snp	C/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75545363	GCCCAAGGCTCAGGG[C/G]TATGGGAATCTGATT	3993
rs566894917	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540459	TGAGGTCCCAGCCCC[A/G]TGTGGGAAGAGCAGC	3993
rs566932569	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75562518	TGTGTCCATGTCTCT[A/G]TCTTGTTCTACATGC	3993
rs567028917	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567181	CTTCAAAGAGGCAGC[A/G]TCAGCCAGGGGCAGT	3993
rs567103819	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75543818	CTGCCATGTCTACCT[C/T]GGCACAGGGTTGTCA	3993
rs567104807	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567576	CCCGGGAGGCGGAGG[G/T]TGCAGTGAGCTGAGA	3993
rs567110451	snp	C/T	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525463	GGCGCGGCGCGCCGT[C/T]CTGCGTCCAGGTGCG	3993
rs567121596	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572735	CGGGAGGCTGAGGCA[A/G]AAGAATTGCCTGAGG	3993
rs567151958	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75559015	CACCCCGCCTCCTCC[A/G]TCCGCACCCCGTGTT	3993
rs567160536	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537254	GCACATCAAGGCCAG[C/G]AGACATGCATGAGCC	3993
rs567370775	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543338	CCACCTGTTTGGGCC[A/G]GGCCTAATCGATACC	3993
rs567373740	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75569408	GAGCCAACCACCTGC[C/T]TAACGCACATTCTGT	3993
rs567375820	snp	A/C	0.00106468	0.0230479	intron-variant, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574156	TCAGTAAGGAGAGAG[A/C]GAGCCAGGCCGAGGA	3993
rs567381074	snp	A/G	3.67013e-05	0.00428361	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574624	GGAGCGGCAACTGGC[A/G]TTCACATCGAGCCGC	3993
rs567459595	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569768	AGATTGTGCCACTGC[A/G]CTCCAGCCTGGGCAA	3993
rs567519316	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570835	AGACGCAGGCCTGGC[A/G]GGTGGCTGGCATGGC	3993
rs567605934	snp	A/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75565437	ACCCTGTTCAGGGGA[A/T]CCCCAAACCTGCTTT	3993
rs567626540	snp	G/T	4.96118e-05	0.0049803	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563804	GCTGACCACTAGGCA[G/T]GGGTAGGTATCCATG	3993
rs567628005	snp	A/G	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75535605	GGTGCCCCAAACAGT[A/G]GCAGGGTGGGAGAAG	3993
rs567649867	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523174	ACAGAGTGAGACTCC[A/G]TTTAAAAAAAAAAGT	3993
rs567689776	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530575	GAATGGTGTGAACCC[A/G]GGAGGCAGAGCTGGC	3993
rs567738182	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529980	GTGTGGTCACTGACC[C/T]GTGCTGAGCTTTGTT	3993
rs567851792	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547485	GTAGGGGAGCAAAAA[C/T]TGGCTTCCCTCCAGC	3993
rs567857752	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75569818	aaaaaaaaaaaaaaa[-/AA]NTGCAGGAGAGCTGG	3993
rs567870582	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559191	GGAGTCAGGGGACCC[C/T]GTCCATGGCATCTCC	3993
rs567934711	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537793	GTTCAGATGGGAAGG[C/T]TTTTTGGAAGGTGAC	3993
rs567965247	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553334	CCCCCCGTCTCCCCC[A/G]ACCTTTTTGTCTCCA	3993
rs568048240	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527598	TTTCTTTTTTTTAAA[C/T]TAAGTTGACCAAATT	3993
rs568098919	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530072	CAGTGAGGGTGGACT[C/T]AACTTCCATGAAGCA	3993
rs568124377	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567806	AGTTAGCTGGGTATC[A/G]TGGCTCACACCTGTA	3993
rs568144660	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549749	CCCTGAGGAGTGCCA[A/G]GGACTCCTCCTCAGG	3993
rs568194161	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561260	GATAAGAATGATCAT[G/T]GTAGGGCTGTTTTTA	3993
rs568230637	snp	A/G	0.00114823	0.0239332	intron-variant	LLGL2	GRCh38.p7	17:75556153	CAAGCTGTATCCTCC[A/G]TCCCCTCGCTCCCAC	3993
rs568237908	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75550986	CCCTGTTCCCAACAA[G/T]ATCCCTTGGGCTTCT	3993
rs568255362	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545439	GATGGCCTGAAATTT[C/G]AGGCCTTGGAAGTGG	3993
rs568268109	snp	C/G			upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525001	ATCGGCCCTTCCCTG[C/G]GCGCAGCGGGGTGCG	3993
rs568292365	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545936	TCCTGTGCGTTGTAG[A/G]TTATTTAGCAGTGTC	3993
rs568349302	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556797	TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG	3993
rs568355277	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523082	TACTCAGGAGGCTGA[A/G]ACAGGAGAATTGCTT	3993
rs568369190	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550583	TGAGTCCAGGAGTTC[A/G]AGACCAGCCTGGGCA	3993
rs568386904	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75528797	TCGCTGTTCATTTAA[A/C]AAATAGAAAAGGCAA	3993
rs568467559	snp	A/G	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75555072	GTACCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG	3993
rs568487332	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535342	GAGGAGAGGAGAGCA[C/T]GGGACATCAGGTGGC	3993
rs568557012	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538876	TAGTTGCTGGATCTT[C/T]GCATCCTCTTTTTCT	3993
rs568568763	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532436	TTTTCTTTGTTTTTT[C/T]GTTTTGAGTCTGAGT	3993
rs568736647	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575566	GGGTGCTGCTGAAGC[A/G]GGGCTGGTACCCAAG	3993
rs568768911	snp	G/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75538263	TGGAGGAGGGAACGG[G/T]GGGTGGGCAGGCCCC	3993
rs568920653	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528519	CAAGTTGGGCCGATC[A/G]CCTGAGGTCAGGAGT	3993
rs569056453	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569830	AAAAATGCAGGAGAG[C/G]TGGGGTTGGACAGAG	3993
rs569087519	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534960	CAGTCCTCCAGTCAT[A/G]CCCCCATTCCCTCTG	3993
rs569298855	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568394	CTGCAGATGCCCTGG[C/T]TCCAACCCTGGAGCT	3993
rs569334831	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557794	TGGTGATAGGCCCCC[G/T]GGGGTGCCGTGTGTT	3993
rs569505009	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529118	CCGAGATCGTGCGAT[C/T]GCACTCCAGCCTGGG	3993
rs569554626	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531850	CTCTCTTCTTCCCAG[A/G]AACCACAGCGAATTC	3993
rs569570597	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571292	CTGAGTCAGCTTCCC[G/T]TGGCTTTATATCCAG	3993
rs569597163	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543022	GGAGGAAGAGGCTTG[C/T]GAAGTTTCCCTTTCT	3993
rs569618479	snp	A/G/T	0.000119992	0.00774487	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563033	TGCCAGAGGAGGCCC[A/G/T]CCACCGGCGTGTGTT	3993
rs569637201	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525488	GGTGCGCGCAGGTGA[A/G]GCCGGGGCGGGCCTG	3993
rs569654929	snp	A/C	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75556904	CGTGGTGGCACATGC[A/C]TGTAATCCCAGCTAC	3993
rs569662273	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538066	TCAGCCCGCCTTGGC[C/T]TCCCAAACTGCTGGG	3993
rs569683736	snp	C/G	0.000798403	0.0199641	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575386	CTGAGCCCGGCGGTG[C/G]CTTCCCTCTGTGGGA	3993
rs569688831	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565547	TTGGGCCATGTTGGC[A/G]CAGAGCGGGGGCCTC	3993
rs569728853	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574879	CCTTCAGCAGAGTGA[C/G]TGGCTGAGCGTCCAG	3993
rs569763665	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570888	GGATCAGCACTGAGC[A/G]AAGCACTGTTCCTGG	3993
rs569776597	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563956	AGGGGAGACAGGGTA[C/G]ACGCTATTCACGTCT	3993
rs569796892	snp	G/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537451	ATAATCCTAGCACTT[G/T]GTGGGGCCGAGGTGG	3993
rs569817632	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526299	GTGTCCCTGCCGGCC[C/G]TTTGTGCCTCCTAAT	3993
rs569818802	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75555125	GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG	3993
rs570014903	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75560586	CTGCTTCCTGGGTTC[A/C]AGCTATTCTCCTGCC	3993
rs570022139	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530732	AGGAGGATCGCTTGA[A/G]CCCAAGAGTTTGAGG	3993
rs570050154	snp	A/G	0.000572497	0.0169092	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524477	CTGTTCTCAGGGACC[A/G]TCTCGGCTGCCTCCT	3993
rs570111033	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539310	AAGTGATCCTCCCAC[C/T]GTAGCCTCCCAAAGT	3993
rs570169914	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561749	AACATGGCGAAACCC[C/T]GTCTCTACTAAAAGT	3993
rs570191278	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75558866	CTCCATCCGCACCCC[A/G]CCTCCTCCATCCGCA	3993
rs570259692	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556228	TTTCCTTCCTTGCCC[A/G]TGGGCTGTTGGGATA	3993
rs570484846	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567980	AGACAAATGGTTTAA[C/T]CATCCAGCGCACATT	3993
rs570493310	snp	C/G	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75528395	GCTGGGATTACAGGC[C/G]TAAGCCACCGCGCCC	3993
rs570545150	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545244	CTTGATTGTCCCACT[C/T]CCAGGCCTGGGGGTG	3993
rs570580416	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75539149	CTGCAGCCTCAACTT[A/C]CCAGGCTCAGCAATC	3993
rs570621376	in-del	-/A	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75555585	AGCCCAGAGCAGGGC[-/A]GGGCCTCCGCGGTAC	3993
rs570628612	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75551091	CCCTGGGAGACAGGT[C/T]ATTTACACATGAAAC	3993
rs570669537	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75548172	CTGAAATCTAAAACC[C/T]TCTATTCGCAATCAT	3993
rs570674867	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531552	TCTTAGGTGATATCG[C/T]TCTCAGGGTTCCTCC	3993
rs570694488	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541523	GTTTCCCGGCCACCT[A/G]CTCTTCCCCAGCAAA	3993
rs570778890	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75561948	AATTAAATATTGAAT[A/G]TTAAAGTCCCCTTCA	3993
rs570897398	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549398	GGGCAAACAGGCTGC[C/T]GTGCTTGCCCGGCTG	3993
rs570924814	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535761	TTGAGCTCTTGAGAT[A/G]GAAGGCGGGCCAGGG	3993
rs570978504	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567500	AAAAATTAGCCAGGC[A/G]TGGTGGTGAGTGCCT	3993
rs571089585	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572176	TTGCAGTTGGTGTCT[C/G]AGGGGCTGCAGAAGT	3993
rs571119802	snp	C/G/T	5.29388e-05	0.00514462	intron-variant	LLGL2	GRCh38.p7	17:75571882	ACCAGCCCCAACACC[C/G/T]ACCTCCTCCCCCTAG	3993
rs571153276	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532496	TGGCATGATCTTGGC[C/T]CACTGCAACCTCTGC	3993
rs571190538	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543319	TGGAGAGAGAGGCCC[A/T]GCTCCACCTGTTTGG	3993
rs571278785	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574266	AGTGATGAGAGTGAG[C/T]TGGGTGGGAGAGGGT	3993
rs571330851	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75547417	GTAAGACACAGTGGA[C/T]GCATTACTTAGCCTC	3993
rs571361552	snp	C/T	0.00015604	0.00883152	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573247	GGACGTCAGTGGCAT[C/T]GCCTCCTGCGTCTTC	3993
rs571399218	snp	G/T	0.000310655	0.0124592	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564546	GCCCAGGGTTAGGTG[G/T]GGGAGGCATGGGGCA	3993
rs571458192	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75533069	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC	3993
rs571507352	in-del	-/AA	0.496105	0.0439572	intron-variant	LLGL2	GRCh38.p7	17:75569802	AGCAAGACTTGTCTC[-/AA]AAAAAAAAAAAAAAA	3993
rs571609480	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75550801	AAAAAAAAAAAAAAA[A/C]AAACACACACACACA	3993
rs571635058	in-del	-/TTTTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75533309	TGGCCCTTTTTTTTT[-/TTTTTTTTTTTTTT]GAGATGGAGTCTCAC	3993
rs571636086	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569348	GCTGGGCTGGGGAGG[A/G]GGAGCTGGGGAGGAG	3993
rs571733619	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539004	CTCCACTGATCTTCC[C/T]GCCTCAGCCTCCCAA	3993
rs571851387	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75573863	CTCAGGACAGGCTGC[A/G]CCATTGACTTGTTCT	3993
rs571855326	snp	C/T	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75558779	CACACTCAGGTGCTC[C/T]GAGTGGAGTGGGCGG	3993
rs571855361	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552643	CAGTTCAGACATTAA[A/T]TCTTTTTTGGAAGTA	3993
rs571989235	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526317	TGTGCCTCCTAATCC[C/G]CGGACGCAGGAAGCC	3993
rs572047193	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554762	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	3993
rs572073106	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525552	CGCGCTTCCCGGGGC[A/C]GCGGATTGGCAGGAG	3993
rs572083028	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559961	AGAAGGGGACGGGGC[A/C]CAAAAAAAGAGAGGA	3993
rs572111781	snp	C/T	0.00363007	0.0424483	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574505	CCGCGGGTGAGGCAC[C/T]GCCCAGGCCAGCTGG	3993
rs572136195	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544473	TTGGTTGTATTTTTG[A/T]TATTGATTTGAGAAC	3993
rs572166598	snp	C/T	3.31044e-05	0.0040683	intron-variant	LLGL2	GRCh38.p7	17:75558114	AAGGCAGGCAGGGGA[C/T]GGTGTCCGACCTTCC	3993
rs572173244	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553562	AGGAAAGCCCAGGGC[C/G]TAAGGAGGCTGCCTC	3993
rs572308225	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75544057	AGCCGGAGTTGGCCT[C/T]GGACTACCCCAATCC	3993
rs572323451	snp	A/G	3.4559e-05	0.00415672	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570971	GAGGGGAGTGCCAAG[A/G]CTGAGCGGCCAGGCC	3993
rs572334053	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555229	GCAGAAGACTCGAAG[A/G]ATGTACACTTAGGTT	3993
rs572374025	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75543506	AGTTTAACAAGGTAA[A/G]TTAGGGAGAGCAGGG	3993
rs572393947	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543232	GCCTCTAGATCTGAG[C/T]GTGGGGAAGCCAGGG	3993
rs572395853	snp	A/G	0.00016007	0.00894479	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574672	GCAATGGCGGAGGTG[A/G]GGGCTCTGGGCTTGA	3993
rs572431459	snp	C/T	0.000244529	0.0110546	intron-variant	LLGL2	GRCh38.p7	17:75570524	AGGTGAGGCTGCGGC[C/T]GGCCACGCACCCAGG	3993
rs572496317	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75536118	AGGCTGGTCTGGTGA[C/G]AGGCAGGAGTGGAGA	3993
rs572610734	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525086	CTCCGCGCCCTTTCC[G/T]CTCCCGCCTCTCGTC	3993
rs572614558	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564722	TAAAAAAATTAGCCA[A/G]GTGTTGTGGCACGTA	3993
rs572675692	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531088	CTCCTCACCCTGCTG[G/T]GTGGCAGGGCAGAGA	3993
rs572691933	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75531574	GGTTCCTCCTGGGGC[A/G]AGGCACGCCAGGTCT	3993
rs572710171	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75540218	TCTGTTCATACCAGG[C/T]GTCTCTAGGCCTGGC	3993
rs572717266	snp	C/T	1.77912e-05	0.0029825	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568981	TTCTGCCCACAGGCA[C/T]GAGGACGGCACGGTG	3993
rs572740694	snp	A/G			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563117	TCGGCTACAGCCGAG[A/G]CCTCGTTGTCATCTG	3993
rs572789656	snp	C/G	3.60347e-05	0.00424453	intron-variant	LLGL2	GRCh38.p7	17:75572994	GGCCATGGGCATGAA[C/G]AACCACCCCACGCCC	3993
rs572855826	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545583	ATTTGGGATCCCGTC[C/T]GCCCTGCCCCTCCCC	3993
rs572864980	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529257	GATGGAGCACAGTGG[C/T]GTGATCTCAGCTCAC	3993
rs572876452	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75572623	TGAGCCGAGATTGTG[C/T]CACTGCCCTCCAGCC	3993
rs572897345	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533412	CAGGTTCACACCATT[A/C]TCCTGCCTCAGCCTC	3993
rs572901879	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526553	CTTGGCTGTGGGGAG[A/C]ACTGACCTAACCAGG	3993
rs572904098	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75547158	GATGCCTCAAAGAGA[A/G]CAAGGACATCGCCCC	3993
rs572912105	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527262	AGATGTCTCAGCTTT[A/G]TTTTATGAACTGGGA	3993
rs572964115	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75550064	TAGGCTGGATGCCGC[A/G]CTTCGGAGGCCCCAG	3993
rs573035893	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532247	AGCTGCTACCATGCC[C/T]AGCTAATTTTTTGTT	3993
rs573072292	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528715	TGCACTCCAGCCTGA[A/G]CAACAAGAGCAAAAC	3993
rs573072339	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534390	GGGGCCCATCCAGCC[C/T]GCGAGCAGGCAGCCC	3993
rs573081145	in-del	-/T	0.000646175	0.017963	intron-variant	LLGL2	GRCh38.p7	17:75571895	CCCACCTCCTCCCCC[-/T]AGCCAAGGAGATCCA	3993
rs573084433	snp	A/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75529387	TTTTTGTATTTTTTG[A/T]AGAGACAGGGTTTCA	3993
rs573173803	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527994	GGGTTTTGCCATGTT[G/T]CCCAGGCTAGTCTTG	3993
rs573209947	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533648	TGGTTCTAGATGTTG[A/G]ATGTGATCCTTAAAC	3993
rs573265683	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541806	CTGATCTTGGCTCAC[A/T]GCAACCTCCGCCTCT	3993
rs573297064	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530432	GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCG	3993
rs573323900	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539113	ACCTAGGCTAGAGTA[C/T]AGTGGTGGGTTCATA	3993
rs573350285	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539656	TCCGTCACCCAGACT[A/G]GAGTGCAGTGGTGCG	3993
rs573364161	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571616	CTGGTTGCCCAGCTC[C/T]ACCCGACTCCCACGC	3993
rs573399365	snp	A/G	3.39144e-05	0.00411777	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571961	TGCTCGACGGACACA[A/G]CGTACCCCTTCCCGA	3993
rs573412668	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561490	AAATTAGTTGGGCAA[A/G]GCGGCACACGTCTGC	3993
rs573734389	snp	C/T	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75554201	TAGCTCCTGGGGAGA[C/T]TGAGGCAGGAGAATC	3993
rs573777677	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569577	GGAGACCAAGGCAGG[C/T]GGATCACCTGAGGTC	3993
rs573816544	snp	C/T	0.000147423	0.00858427	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570080	GAGCGCCTGGCAGCC[C/T]GCTCAGGGCCCGTGC	3993
rs573934725	snp	C/T	0.000154826	0.0087971	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564590	AGACAGGGCCAGGTG[C/T]AGTGGCTCCTGCCTG	3993
rs574027505	snp	G/T			upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524338	GTCCCTCTGATCTTT[G/T]CCCTGGTGGATCATG	3993
rs574121019	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557926	AGTTGCTCCCACCGG[C/T]CTGACTGGGAAAAAT	3993
rs574198217	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535109	TGGGCACTTGCAAAG[A/C]GGCTACAGGCGTCTG	3993
rs574256156	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541983	TGATCCACCTGCCTC[C/T]GCCTCCCAAAGTGCT	3993
rs574286670	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551780	CCATGTATGTGATTT[A/G]AAATTTCCTAGAAGC	3993
rs574356103	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75530665	AAAAAAAAAAAAAAA[-/AA]TTAGCTGGGCATCGT	3993
rs574356961	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555917	CTCCAACACTCAGGT[A/G]TCTGGGAGGAACCGG	3993
rs574408698	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75560862	TTTTTTTGAGAGAGT[C/T]TTACTCTGTCCCAGG	3993
rs574466766	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549565	CTGGGCCCCTGGTGT[C/T]AGGTGACAGCAGCCA	3993
rs574484780	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544006	ATTCCTTCTGGCTCC[A/G]GCCGGGGTGAGTGGG	3993
rs574494384	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555352	TGCTCTGCCTGCCGG[G/T]TTCGCACCATTCTCC	3993
rs574504278	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539220	ATGCCACCATGCCCA[A/G]CTAATTTTGTTTTTA	3993
rs574563869	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75532677	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	3993
rs574593558	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540014	CCATGCCAAGCTCTT[C/G]CTCCTTCTACAGGAT	3993
rs574594505	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545278	GAGGGAGGCTCCTGG[A/G]TCTCCTGCTCTGCCT	3993
rs574598948	snp	A/G	1.71228e-05	0.00292594	intron-variant	LLGL2	GRCh38.p7	17:75543536	GAAGATGACCCCCAG[A/G]TTTTCGGCCAAGCAG	3993
rs574644583	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75526999	ATAGTGAGACCTCGT[-/C]TCTGCAAATAATAAA	3993
rs574735882	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524193	CTTCCGTAGAATCTC[C/T]TCTCTGGGAGCCCTA	3993
rs574749194	snp	A/C/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561649	AATTAGGCCGGGCGC[A/C/G]GTGGCTCACGCCTGT	3993
rs574749323	snp	A/G	0.000297442	0.0121915	intron-variant	LLGL2	GRCh38.p7	17:75574713	CAACCGTGCTGGGAA[A/G]GGCTGGGAGGAAGAG	3993
rs574754081	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549932	TAACGTTGCAGTCTG[G/T]CGGCTTCTGCAAATC	3993
rs574760926	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75537599	GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC	3993
rs574827686	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75571482	CCTGGCTGGTTCTCC[A/C]CTGCTGTATCACAGC	3993
rs574829595	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565809	CCCTGAAGCTCTCAC[A/G]TAATGGTTCTGCTGT	3993
rs574888650	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541678	TTTGAGATAACTGAC[C/T]GTGCAGATCCTTTCA	3993
rs574909961	in-del	-/TC			intron-variant	LLGL2	GRCh38.p7	17:75527573	AAAAAGTAACTTTTT[-/TC]TCTTTTTTTTTCTTT	3993
rs574965006	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546153	GGTGTGCAGGATGAC[C/T]GTGAAGTCTCTGACC	3993
rs574972805	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532005	GTTTGATGAGAGGGA[A/C]ATCTGGGCACAGGAC	3993
rs575002554	snp	G/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75546541	GGTTGAGTTGGGGGA[G/T]CCTTGGGACAGGCCC	3993
rs575061703	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531596	GCCAGGTCTGCTTGG[C/T]AACGCTGTTTTCCTC	3993
rs575082933	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525696	CCGCCCCAGGCTCGC[C/T]GCGCCGGAGGTGAGC	3993
rs575085942	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533685	AAGATGTCTGCCGTC[A/G]TTGAAAGTTGTTTCT	3993
rs575093249	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526391	GCTTTGGACACCTTC[A/G]CATGACAGTGCGGAG	3993
rs575101503	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552545	TTTGACGTGTGATTA[A/G]CTACTAATGAGATTT	3993
rs575118178	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524669	GAAGAGAGGACTGTG[C/T]GCCTTTAACGAGAGG	3993
rs575212339	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534436	GAGGCCTGACCTGAG[C/T]GGAGGATTCTGCAGT	3993
rs575252818	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75572526	AAAAATTAGTTAGGC[A/G]TGGTGGCGGGCACCT	3993
rs575283391	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75530499	ACTAAAAATACAAAA[A/C]ATTAGCTGGGCATGG	3993
rs575366202	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527349	ACTCAAACTCAGCTC[C/T]TAAGCTTCTAATCAG	3993
rs575481580	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569439	GTCCTTTGCTTTTCC[A/G]GTGGATGGAGGTGGC	3993
rs575765062	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75547447	CTCTGTTCTTTAGTT[A/T]CCTCATCTGTAAAAT	3993
rs575775410	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551345	CCAGTACCATCCCGT[G/T]TATTAGATGAGAAAT	3993
rs575805975	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75556408	AATGGACTGAGGAGA[C/T]ACAGGCTTATTTTGT	3993
rs575819197	in-del	-/A	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75527556	TAAGAAATAAAATAG[-/A]AAAAAAGTAACTTTT	3993
rs575834444	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75548582	AGGCAGGTAGATCAC[C/T]TGAGGTCAGGAGTTC	3993
rs575844281	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567643	GACTCCATCTCAAAA[A/C]AAAAAGAGAAAAAAA	3993
rs575927594	snp	C/G			upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525192	GGGCGCCCCCCCGCA[C/G]CCCCCCCCGAGGAAA	3993
rs575939721	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524847	GAGATCCGCTTCCTC[G/T]GGTGCGGGATCTAAG	3993
rs576054028	snp	G/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75535679	TCTGCCACTTAGAGC[G/T]AGGGGGGCCCAAGGC	3993
rs576085865	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531026	GAGTGCAGGATTAAA[A/C]CTGCTGTGAGTTCTG	3993
rs576237283	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564680	CCAGCCTGGACAACG[C/T]AGGGAGACCCTTGTC	3993
rs576248961	snp	C/T	0.0498117	0.149749	intron-variant	LLGL2	GRCh38.p7	17:75554299	AAGAGCAAAACTCCG[C/T]CTCAAAAAAAAAAAA	3993
rs576274080	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75559558	TCTTGGCTTCCTACC[C/T]GTCACCTACTGAGAA	3993
rs576307916	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75554686	CAAGATGGGCGGATC[A/G]AGACCATCCTGGCTA	3993
rs576366940	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559854	AAGCCTTGACCGCCA[C/T]AGGCATGTGGGTCTG	3993
rs576444227	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75558369	AAAGACCTGGGACCC[C/T]CTCCCTTTCCACAGC	3993
rs576504796	snp	C/T	0.000721191	0.0189757	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568483	TACCCCAGCCTTTGA[C/T]GACCCCTATGCCCTG	3993
rs576593327	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75530502	AAAAATACAAAAAAT[C/T]AGCTGGGCATGGTGG	3993
rs576756416	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75562248	GTTTTGTTTTATGGG[A/G]CTAAAAAACTTCTTT	3993
rs576758256	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550678	TAGTTCTAGCTACTC[A/G]GGAGACTCAGGTGGA	3993
rs576782325	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542522	ACAGAGGCTCCTTCC[C/G]CTTCCCCCAAGGATA	3993
rs576818125	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543169	AGCTTTTCCTACCCC[A/C/G]ATTATAAGGCCACAG	3993
rs576933987	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544364	TCGTTGGGGGCTTCC[A/G]TTTGGGCTCCCCTGC	3993
rs576979968	snp	A/C	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567754	CAACACCAGCCTGAG[A/C]AACATGGCGAAACCC	3993
rs577005187	snp	A/G	1.69312e-05	0.00290952	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569316	GGCTGTGGCAGGCAC[A/G]GCAGGGCAGGTAGCA	3993
rs577046177	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555436	ACAGTGTGTGTGTGT[A/G]TTCTGTAATAAATGA	3993
rs577065178	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533326	TTTTTTTTTTTTGAG[A/G]TGGAGTCTCACTCTG	3993
rs577092979	snp	C/T	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75529721	CAAAAATTAGCTGGG[C/T]GTGGTGGTGCGTGCC	3993
rs577127383	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533584	GCTGGGATTGCAGGC[A/C]TGAGCCACCGCGCCC	3993
rs577169327	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75535090	TGGGCTTCCCAGGGC[A/G]ACATGGGCACTTGCA	3993
rs577184368	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75532104	TTTTTTTTTTGAGAC[A/G]GAGTCTTACTCTGTG	3993
rs577248333	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527654	TTAATTTGTAGAGAT[A/G]GGATCTCACCATATG	3993
rs577249125	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540083	CTGTCTCTGGAGGCC[A/G]TGTGGCTTGGGGGAG	3993
rs577279678	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575683	ACTGTATGGCCAGTG[C/T]GTGGGGTTCTCCGGT	3993
rs577330291	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542294	AGGTGTTCCCTCTCC[C/T]TCCTGCAGTCAAAGC	3993
rs577356342	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534543	TGGAGCACAGTGGTG[C/T]CATCATAGCTCACTG	3993
rs577360690	snp	A/C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75527030	AAAAGTTAGCCAGGC[A/C/G]TGGTGGCGTGCACCT	3993
rs577391770	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75552929	TGTAGGGCATTTCCA[C/T]CAGAGTCCTCCAAAT	3993
rs577393786	snp	C/G	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75558938	CCCACCTCCTCCATC[C/G]GCACCCCGCCTCCTC	3993
rs577409355	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575190	GAAAAAGTTTTTAAT[A/C]AACACCTATTACCTC	3993
rs577463412	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566404	CTCAGCTTGGGCTGC[A/G]GTGCAGGCCATGGGA	3993
rs577695423	snp	A/G	0.000119199	0.00771914	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569111	GCCCAGGGCGAGGAC[A/G]AGTGGCCCCCACTCC	3993
rs577804604	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573408	GAGGGAGCACTAGCC[C/T]CTACTCCCCCAGGTG	3993
rs577834768	in-del	-/C	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75534105	GGTGGTCCATCTTCT[-/C]CCCAGAATGGTTTTG	3993
rs577841325	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75573747	CACGAGCTCAGCCCA[C/T]CCTCCCAGGCTCCGG	3993
rs577895729	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523455	GACTCCTACCCCTAC[G/T]CCTAGCTCTGAGCAA	3993
rs577921072	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75537529	TGAAAACCACAGCTC[A/T]ACTAAAAATAACAAA	3993
rs578003133	snp	C/G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534486	GGGCTTGGATTTTTT[C/G/T]TTTTCTTTTTTTGAG	3993
rs578012356	snp	C/T	0.00164961	0.028672	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568447	GCTTCCTCCTGGCCC[C/T]GGCCCCTGACCCTTG	3993
rs578055504	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75557348	AGAGTGGAGAGGGCT[A/C]TGCCTGGCAGGGACA	3993
rs578113452	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75546584	GAGGGCAGGTCCAGC[A/G]GACAGGCGGAGGGCA	3993
rs578161863	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551465	CCCTGTTCTAAATCA[C/G]CCTTTGGAAAAGAAG	3993
rs578171415	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532322	GTGGCGCGATCTCAG[C/T]CCACTGCAAGCTCCG	3993
rs578173405	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75562737	CCACGCCCAGCTAAT[A/G]TTTTATATTTTTAGT	3993
rs578220451	snp	C/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75537852	CTCTCTCTGTTGCCC[C/T]GGCTGTATTACAGTG	3993
rs587784476	in-del	-/C			frameshift-variant, upstream-variant-2KB, intron-variant, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523684	GGAGAAGTCTGGGGG[-/C]TTGGAAATCATCTTT	3993
rs587784477	snp	C/T			upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524342	CTCTGATCTTTGCCC[C/T]GGTGGATCATGGTGA	3993
rs745328225	in-del	-/A	3.35278e-05	0.00409424	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524474	TGTCTGTTCTCAGGG[-/A]CCATCTCGGCTGCCT	3993
rs745340362	snp	C/G	1.68071e-05	0.00289884	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573152	CACCACCTGGCAGTC[C/G]TTACCAACCTGGGCG	3993
rs745341401	snp	A/C	1.8014e-05	0.00300111	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574692	TCTGGGCTTGAGTGC[A/C]GCTGCCAACCGTGCT	3993
rs745356525	snp	A/G	1.9386e-05	0.0031133	intron-variant	LLGL2	GRCh38.p7	17:75568918	TGAGGTGGACGAGCC[A/G]GCCCCTGGGCATCCC	3993
rs745357381	snp	A/G/T	6.59319e-05	0.00574127	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523658	GTTTCTCATTGTATT[A/G/T]TCAGGCTGTTGGAGA	3993
rs745372373	snp	A/C/G	4.06473e-05	0.00450803	intron-variant	LLGL2	GRCh38.p7	17:75558025	GCTCCATGCATGGGT[A/C/G]CTGCTGCCTCGGGGG	3993
rs745409371	snp	C/T	8.72087e-05	0.00660278	intron-variant	LLGL2	GRCh38.p7	17:75570333	GCAGCACTGACAGCC[C/T]GCCATCCCCCCAAGG	3993
rs745413496	snp	A/G	5.28769e-05	0.00514156	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568793	CCAATTGATGGTGGC[A/G]CCAGCCTGACCCCAG	3993
rs745446822	snp	A/G			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524112	CCAGTGCTCTGGGGC[A/G]CTCTTCATCAGAGCC	3993
rs745460281	snp	A/C	0.000148735	0.00862236	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563766	GGTCCCTTTCCTTGC[A/C]AAGCGATTACCAGAA	3993
rs745461828	in-del	-/TTT			intron-variant	LLGL2	GRCh38.p7	17:75548281	AATTTTTTTTTTCCT[-/TTT]TTTTTTTTTTTTGGA	3993
rs745474839	snp	C/T			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569079	TCACCGACACGGACC[C/T]CAACGAGAACTTCAG	3993
rs745515843	in-del	-/C	1.93321e-05	0.00310897	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568450	TCCTCCTGGCCCCGG[-/C]CCCTGACCCTTGCCC	3993
rs745578088	snp	C/G	1.67708e-05	0.00289571	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523750	AAAGAATAACCCTGG[C/G]AAACCCTATGCCCGG	3993
rs745654893	snp	C/G	1.70496e-05	0.00291967	missense, intron-variant	LLGL2	GRCh38.p7	17:75564537	GGAGTGGGTGCCCAG[C/G]GTTAGGTGTGGGAGG	3993
rs745656145	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75556541	GGGGTGAGGCTGCTG[A/G]GGGGCTCAGAGACCT	3993
rs745709991	snp	A/G	6.65757e-05	0.00576918	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564463	TCGACTTCACCTCCC[A/G]TGTCATCGGCTTCAC	3993
rs745721034	snp	C/T	1.65908e-05	0.00288012	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569250	CCCCTACAGTGATGA[C/T]CCCCGGCTGGGCATC	3993
rs745729649	snp	A/G	1.70688e-05	0.00292132	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573551	GCTGGTGGAGCCCCG[A/G]TGTCTGGTGGATTCA	3993
rs745780613	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528543	CAGGAGTTTGAGAGC[A/G]GCCTCACCAACATGG	3993
rs745825946	snp	A/G	2.87898e-05	0.00379395	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570241	CCACCAGCAGCGGCG[A/G]CAGGTCTTTGTTAAG	3993
rs745841597	snp	A/G/T	3.322e-05	0.00407542	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556115	CTGCGCATCCTGGCC[A/G/T]TCGGCACCCGTTCTG	3993
rs745842538	in-del	-/TT			intron-variant	LLGL2	GRCh38.p7	17:75530646	CAGAGCGAGACTCCA[-/TT]TCAAAAAAAAAAAAA	3993
rs745871996	snp	C/G	1.82042e-05	0.00301691	intron-variant	LLGL2	GRCh38.p7	17:75572972	CACAGGGCAGGAGAA[C/G]TGGTTTGGCCATGGG	3993
rs745888530	in-del	-/TTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75557035	CTCTGTCTCAAAAAC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGT	3993
rs745938438	snp	C/T	1.68086e-05	0.00289896	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563149	GACCTACAGGGCAGC[C/T]GCGTGCTCTACCACT	3993
rs745939163	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75548166	AAGATTCTGAAATCT[A/G]AAACCCTCTATTCGC	3993
rs745990143	snp	C/T	0.000297575	0.0121942	intron-variant, utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574199	GGCGCCCTGACCCGG[C/T]CTCTACCTTCCAGAG	3993
rs746007049	snp	C/T	1.6654e-05	0.00288561	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568600	GCACTGTTCCGCCAT[C/T]ACCTGCTCTCACCAC	3993
rs746020983	snp	A/G	1.77263e-05	0.00297705	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572053	CTCGTCGTATCAGAG[A/G]AGCAGTTCAAGGTGC	3993
rs746100598	snp	C/T	1.65192e-05	0.00287391	intron-variant	LLGL2	GRCh38.p7	17:75558149	CTTTCCTGAGCCTAC[C/T]CCTAGCTACGGAGCC	3993
rs746112891	in-del	-/CTCCCGCCC	0.000149893	0.00865587	intron-variant	LLGL2	GRCh38.p7	17:75573654	AAGGGCCAGAGGCCT[-/CTCCCGCCC]CTCCCGCCCCTCCCG	3993
rs746116098	snp	C/G	6.64386e-05	0.00576323	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570487	CGGCACCCGGCTGGC[C/G]CCCCAGGAGAGGTGA	3993
rs746149218	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75570667	GCTGCTTCTCTCTGC[-/CT]CAGCTTCCTGAGCAG	3993
rs746164279	snp	G/T	1.90696e-05	0.00308779	intron-variant	LLGL2	GRCh38.p7	17:75569949	CTTGCTGAGCCACCT[G/T]CCACCCTGCGCAGGT	3993
rs746228748	snp	A/G	3.32546e-05	0.00407752	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543480	GGAGAGGCTCAAGCG[A/G]GACCTGTTCCAGTTT	3993
rs746353064	snp	C/T	0.00010345	0.00719127	intron-variant	LLGL2	GRCh38.p7	17:75573916	GCCGGGCAGGGAGCC[C/T]GGGGGCCCTGGTCCT	3993
rs746409769	snp	A/G	1.68216e-05	0.00290009	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568518	TGCTGGCTGAGGAGG[A/G]GCTGGTGGTGATTGA	3993
rs746416058	snp	C/G	1.73084e-05	0.00294175	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570031	GGAGGCCGACCTGCT[C/G]CAGGACCAAGAGGGC	3993
rs746424760	snp	A/G	1.72371e-05	0.00293568	intron-variant	LLGL2	GRCh38.p7	17:75555995	TGCAGCAGCCATGGT[A/G]GCGCGAAGGGGACAG	3993
rs746451996	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75548434	AGGCATGTGCCACCA[A/C]GCCCGGCTAAAGGAC	3993
rs746494112	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75545192	GCAAGGAGTTGTCCC[A/T]TCTTCTTTCCCCTAT	3993
rs746504780	snp	A/G	1.64779e-05	0.00287031	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524226	GCTTAGGAGTGGGCT[A/G]TGGCTGGGTCTCACT	3993
rs746509659	snp	A/G	1.65269e-05	0.00287457	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563778	TGCAAAGCGATTACC[A/G]GAATCCTCTGGCTGA	3993
rs746510002	snp	C/T			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571700	CGCTGTGGGCTGGCA[C/T]CAATGGGGGCACCAT	3993
rs746563105	snp	A/G	1.70749e-05	0.00292184	intron-variant	LLGL2	GRCh38.p7	17:75563489	CACCCGCCGGGCAGG[A/G]CCCACCCCCAGTGCC	3993
rs746563125	snp	A/G	1.74903e-05	0.00295717	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568999	GGACGGCACGGTGCG[A/G]TTCTGGGATGCCTCG	3993
rs746576237	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75534547	GCACAGTGGTGCCAT[C/T]ATAGCTCACTGCAGC	3993
rs746580615	snp	A/G	1.68337e-05	0.00290114	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559314	CCTGCGAGCTGCTCT[A/G]CCTGGGCACCGAGAG	3993
rs746591952	snp	A/G	3.30355e-05	0.00406407	utr-variant-3-prime, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574902	GCGTCCAGGCTGCGC[A/G]ATGAGCACACACTAC	3993
rs746626804	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75556360	CCTGGTGGGATGCGA[C/T]CCTGTCCTTTGCAGG	3993
rs746669269	snp	A/G	1.65707e-05	0.00287838	intron-variant	LLGL2	GRCh38.p7	17:75563841	CTCTTTCCTCTCCAG[A/G]GCCTTCCTGGAGGGC	3993
rs746702735	in-del	-/AC			intron-variant	LLGL2	GRCh38.p7	17:75560103	TGGACTGGGCCTGGG[-/AC]ACACTCCTGCAGCTG	3993
rs746716138	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530542	GTAGTCCCAGCTGCT[C/T]GGGAGGCTGAGGCAG	3993
rs746756736	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539791	TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC	3993
rs746789115	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75555600	AGGGCCTCCGCGGTA[C/T]TCTAGGCCCCTGGGT	3993
rs746796443	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527696	GGTCTCAAACTCCTG[A/G]ACTCAAGTGACCCTC	3993
rs746806874	snp	C/T	0.0001064	0.00729306	intron-variant	LLGL2	GRCh38.p7	17:75557965	GATCAGGTCACTGGC[C/T]TGGTGCCCCAGGGCC	3993
rs746807968	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567357	TAATCCCAGCTACTC[A/G]AGAGGCTGAGGCAGG	3993
rs746842601	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528407	GGCGTAAGCCACCGC[A/G]CCCGGCCTTAAATAA	3993
rs746891607	snp	A/C	3.67235e-05	0.00428491	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574702	AGTGCAGCTGCCAAC[A/C]GTGCTGGGAAGGGCT	3993
rs746921008	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75538647	CACAGGTAATCAACA[A/G]GATTAATAAGTAAGC	3993
rs746967865	snp	C/T	5.55314e-05	0.00526902	intron-variant	LLGL2	GRCh38.p7	17:75558035	TGGGTCCTGCTGCCT[C/T]GGGGGAGGGCAGCCC	3993
rs746969863	snp	A/G	3.85253e-05	0.00438875	intron-variant	LLGL2	GRCh38.p7	17:75568934	GCCCCTGGGCATCCC[A/G]GCTGGCATCCCTCTC	3993
rs746999569	snp	A/C	7.38184e-05	0.00607485	intron-variant	LLGL2	GRCh38.p7	17:75570914	CCTGGGGAGGGGAGT[A/C]CAGAGCTGACCCTTA	3993
rs747050547	snp	A/G	3.41151e-05	0.00412994	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569105	TTCAGTGCCCAGGGC[A/G]AGGACGAGTGGCCCC	3993
rs747157056	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542448	GTGTTTCCCAAGGAC[A/G]GGCCTTGCTGTCCTG	3993
rs747177188	snp	A/T	7.79757e-05	0.00624354	intron-variant, missense	LLGL2	GRCh38.p7	17:75570502	CCCCCAGGAGAGGTG[A/T]GGCCTGAGGTGAGGC	3993
rs747196545	snp	C/T	3.89917e-05	0.00441524	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524508	GTACCCAGACTCTAA[C/T]CTGTAGCTTCAGAGG	3993
rs747216083	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529816	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	3993
rs747241229	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75556862	AAAACCCTGTCTCTA[C/T]TAAAAATATTTTAAA	3993
rs747268584	snp	C/T			synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569024	GCCTCGGGTGTCTGC[C/T]TGCGGCTGCTCTACA	3993
rs747288449	snp	C/T	0.00035685	0.0133528	intron-variant	LLGL2	GRCh38.p7	17:75558493	AAGACCACATGATCC[C/T]GTCGTGTGCCCTCGC	3993
rs747320876	snp	C/T	6.65591e-05	0.00576846	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568615	CACCTGCTCTCACCA[C/T]GTCTCCAACATCCCG	3993
rs747378240	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551479	AGCCTTTGGAAAAGA[A/G]GGTGGGGATGGGGGG	3993
rs747388437	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552746	AGCCCCTGTTCTTCT[A/G]GAACCCGAGTTGTTC	3993
rs747409735	snp	C/T	1.77175e-05	0.00297631	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570050	GACCAAGAGGGCTAC[C/T]GCTGGAAGGGGCACG	3993
rs747473434	snp	A/G	0.000148249	0.00860829	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523298	CTTCAGCATATCTCT[A/G]TGCTGCAGACAACAC	3993
rs747492699	snp	A/G	1.80474e-05	0.0030039	intron-variant	LLGL2	GRCh38.p7	17:75572991	TTTGGCCATGGGCAT[A/G]AACAACCACCCCACG	3993
rs747498972	snp	A/G	9.44956e-05	0.00687305	missense, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574494	CTGGAGGGAGACCGC[A/G]GGTGAGGCACCGCCC	3993
rs747532920	snp	G/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524066	CAGGCTAAGAGTGGT[G/T]AGCACCTTGCTCTTC	3993
rs747571772	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75546899	ACCCAGGGCTGGAGC[C/T]TGGAGCGGCACGTGG	3993
rs747595996	in-del	-/AACA			intron-variant	LLGL2	GRCh38.p7	17:75549479	TCCCCTTAGGCCCTG[-/AACA]AACAGTGTGTTCCTG	3993
rs747636430	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551740	GTGTGCGGAATTGTC[A/G]AGGCCAATGGGAATA	3993
rs747655578	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75543602	AAGGTATAGCTCTTA[C/T]GTGACTGCCTGCAGT	3993
rs747678898	snp	C/T	5.07593e-05	0.00503756	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571716	CAATGGGGGCACCAT[C/T]TATGCCTTCTCCCTG	3993
rs747727520	snp	A/C	1.70901e-05	0.00292314	intron-variant	LLGL2	GRCh38.p7	17:75573468	GGCCGCTAGCATTGC[A/C]CCCACTCCCCAGGCT	3993
rs747807853	snp	A/G	5.94831e-05	0.00545326	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574298	GGGCTGGCAGGAGGG[A/G]TGGGGAAGGGGGGTC	3993
rs747849122	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75554035	GGCCGGGTATGATGG[C/T]TCACACCTGTAATCC	3993
rs747879322	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566341	CCATGTGGGGGACAC[A/G]GAGTGGAGCAAAGAC	3993
rs747913219	snp	C/T	1.65192e-05	0.00287391	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574914	CGCGATGAGCACACA[C/T]TACTACTGATGGCCT	3993
rs747922152	snp	A/G	3.5176e-05	0.00419366	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569028	CGGGTGTCTGCCTGC[A/G]GCTGCTCTACAAACT	3993
rs747923819	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536679	TAGGAGGCAGATAAA[C/T]AAAAAGGAGAAAAAA	3993
rs747969440	snp	A/G	3.30404e-05	0.00406437	intron-variant	LLGL2	GRCh38.p7	17:75558143	CCAGAGCTTTCCTGA[A/G]CCTACTCCTAGCTAC	3993
rs747971131	snp	A/T	1.83212e-05	0.0030266	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574704	TGCAGCTGCCAACCG[A/T]GCTGGGAAGGGCTGG	3993
rs748070159	in-del	-/TTTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75557035	CTCTGTCTCAAAAAC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGTG	3993
rs748070944	snp	A/C	1.73555e-05	0.00294575	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569089	GGACCCCAACGAGAA[A/C]TTCAGTGCCCAGGGC	3993
rs748082392	snp	A/G			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573980	CAGAGTGATGGCGAG[A/G]GTAAGACAGGCCTCC	3993
rs748131735	snp	A/C	1.6477e-05	0.00287024	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524259	AACCCTTTGTCCCTG[A/C]AGATTTGATGAGCCT	3993
rs748151823	snp	C/T	3.30546e-05	0.00406524	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563783	AGCGATTACCAGAAT[C/T]CTCTGGCTGACCACT	3993
rs748188898	snp	A/C	5.18166e-05	0.00508976	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573583	CAGAAACCAAGAACC[A/C]CCGCCCTGGTAACGG	3993
rs748216459	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557471	CAGAGATGAAAAACC[A/G]GATCAGGTTGGGCAC	3993
rs748251600	snp	A/G	2.40625e-05	0.00346852	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524527	TAGCTTCAGAGGCCA[A/G]TCTGGGCCTTGGCCC	3993
rs748269615	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75556741	GGGACCCCTCTTGTC[C/G]CTAGGGATGTTTTTA	3993
rs748277859	snp	A/G	1.67809e-05	0.00289658	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571010	ATGGAGCTGGCGCCT[A/G]TGCAGCGCAAGATCG	3993
rs748296570	snp	A/G	1.66333e-05	0.00288381	intron-variant	LLGL2	GRCh38.p7	17:75569188	CTGGGTCCTGTCCCC[A/G]TGGCTGCTCACAGGG	3993
rs748313959	in-del	-/AAAAT			intron-variant	LLGL2	GRCh38.p7	17:75529564	TCTCTTTAAAAACAA[-/AAAAT]AAAAAAAAATTAGGC	3993
rs748350453	snp	A/G	7.23223e-05	0.00601298	intron-variant	LLGL2	GRCh38.p7	17:75573636	AGCCGAGCCAGGTGA[A/G]TGAAAGGGCCAGAGG	3993
rs748363376	snp	C/T	1.66208e-05	0.00288273	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543445	AGGCGGTTCCTGAGG[C/T]CAGGGCATGACCCTG	3993
rs748444648	snp	C/T	4.94205e-05	0.0049707	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523315	GCTGCAGACAACACA[C/T]CTTCCTGATGGAGGT	3993
rs748459461	snp	A/G	5.06316e-05	0.00503123	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573084	AGGGCTCAAGAGTGC[A/G]GCGGGTCAGCGTGGC	3993
rs748493884	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527257	GCGAGAGATGTCTCA[A/G]CTTTATTTTATGAAC	3993
rs748525082	snp	A/G/T	6.71033e-05	0.00579204	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563110	ATCCTGATCGGCTAC[A/G/T]GCCGAGGCCTCGTTG	3993
rs748525789	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534507	TTTTTTTGAGAAAAG[A/G]TCTCGCTCTGTCACC	3993
rs748554837	snp	A/C	3.32701e-05	0.00407847	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568681	CCGGCAGAACGCACA[A/C]TTCTCCACCATGGTA	3993
rs748626837	in-del	-/GGGCATCCCGGC	1.93823e-05	0.003113	intron-variant	LLGL2	GRCh38.p7	17:75568925	GACGAGCCAGCCCCT[-/GGGCATCCCGGC]TGGCATCCCTCTCAC	3993
rs748627925	snp	C/T	0.000133565	0.00817096	intron-variant	LLGL2	GRCh38.p7	17:75558498	CACATGATCCCGTCG[C/T]GTGCCCTCGCCAGTG	3993
rs748630833	snp	A/G	1.64735e-05	0.00286993	intron-variant	LLGL2	GRCh38.p7	17:75558253	TGAGGGACCTGGGGT[A/G]GGACAGGAAGCCACT	3993
rs748658527	in-del	-/CA	4.21825e-05	0.00459233	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524558	TGGGTGTCTGATACT[-/CA]CAGAGTGAAACTGTG	3993
rs748662977	snp	A/G	1.69628e-05	0.00291224	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563380	GCCTGCTCGTCAGCT[A/G]TCACTCTGACGGCAG	3993
rs748704804	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572825	ACTCCATCTCGGAGG[A/G]AAAAAAAAAAAATCC	3993
rs748709269	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75538914	CTTTTTTTTAGAAAC[-/AA]AAGAGTCTCGCTCTG	3993
rs748716818	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75569803	GCAAGACTTGTCTCA[-/AA]AAAAAAAAAAAAAAA	3993
rs748742183	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528983	CCCACACAGTGAAAC[C/T]GGTCTCTACTTAAAA	3993
rs748801213	snp	C/T	1.66601e-05	0.00288614	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556103	TACAGCCCGTCCCTG[C/T]GCATCCTGGCCATCG	3993
rs748816820	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75527285	AACTGGGATTTGGGG[G/T]TTAGTTTTCTTAGGC	3993
rs748876669	snp	C/T	1.7865e-05	0.00298867	intron-variant	LLGL2	GRCh38.p7	17:75571852	AGGGAGTGGCTCCAG[C/T]CCTGCCACCCCCTCA	3993
rs748906294	snp	C/T	1.81721e-05	0.00301425	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574636	GGCGTTCACATCGAG[C/T]CGCCGTGGGGTGCAG	3993
rs748938750	snp	G/T	0.000295075	0.0121429	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573090	CAAGAGTGCGGCGGG[G/T]CAGCGTGGCCCACTT	3993
rs748939656	in-del	-/CCAGCACTGCC	1.86635e-05	0.00305473	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523792	TGGGTACGCAGTGAG[-/CCAGCACTGCC]CCTCCCCCAGCTGCT	3993
rs748999529	snp	A/G	1.64743e-05	0.00287	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523331	CTTCCTGATGGAGGT[A/G]CCCGGTAAGTTTCCA	3993
rs749001753	snp	C/T	3.46963e-05	0.00416497	intron-variant	LLGL2	GRCh38.p7	17:75568765	ACTTCTTGGTCTCTT[C/T]TTCTAGGAGTGGCCA	3993
rs749050426	snp	C/T	1.69766e-05	0.00291342	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573488	CTCCCCAGGCTTCTA[C/T]CTGATCTCACCCTCG	3993
rs749071763	snp	A/G	1.68337e-05	0.00290114	intron-variant	LLGL2	GRCh38.p7	17:75569156	GGAGCCTGGGACCCA[A/G]GAAGGGCAGAGGCCA	3993
rs749096965	snp	C/T	4.94295e-05	0.00497115	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524383	TACAGCTTCAGGGAC[C/T]TCACGTTGCCCCAGG	3993
rs749098773	snp	C/T	1.78595e-05	0.00298822	intron-variant	LLGL2	GRCh38.p7	17:75564340	CCCACTGCCGCTCCT[C/T]TGTGCCTGCCAGGTT	3993
rs749122180	snp	C/T	1.70726e-05	0.00292164	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569099	GAGAACTTCAGTGCC[C/T]AGGGCGAGGACGAGT	3993
rs749182625	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75536931	CTCCCGAGTTCAAGC[-/A]GTTCTCCTGCCTCAG	3993
rs749188667	snp	A/G	1.66405e-05	0.00288443	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564450	CAGCAGACGGCCTTC[A/G]ACTTCACCTCCCGTG	3993
rs749212547	snp	C/T	1.7056e-05	0.00292022	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573547	AGTGGCTGGTGGAGC[C/T]CCGGTGTCTGGTGGA	3993
rs749218398	snp	A/G	3.39046e-05	0.00411718	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571772	TGGATGAGCCTGTGC[A/G]GGCAGAGCAGGGTGA	3993
rs749278321	snp	A/G	1.66868e-05	0.00288845	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559332	TGGGCACCGAGAGTG[A/G]CAACGTGTTTGTGGT	3993
rs749285301	in-del	-/C	1.70051e-05	0.00291586	intron-variant	LLGL2	GRCh38.p7	17:75543529	GAGCAGGGAAGATGA[-/C]CCCCAGGTTTTCGGC	3993
rs749285333	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75533973	CAATCCCCACCTCCT[C/G]GAGCTGACATCTGGA	3993
rs749287012	snp	C/T	0.000311704	0.0124802	intron-variant	LLGL2	GRCh38.p7	17:75573903	CAGGGCTCTCAGAGC[C/T]GGGCAGGGAGCCCGG	3993
rs749296613	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557701	GCTCAGCCTTCCCTC[A/G]GCTGGTTAATCATTG	3993
rs749299653	snp	A/G	1.69709e-05	0.00291293	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571954	ATCCTGGTGCTCGAC[A/G]GACACAGCGTACCCC	3993
rs749300605	in-del	-/AAAA			intron-variant	LLGL2	GRCh38.p7	17:75548756	GTGAGATTCTGTCTC[-/AAAA]AAAAAAAAAAAGCCA	3993
rs749334626	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75550204	GGCTATGCCCCGTCC[C/T]GCCCTCTGTCCTGAG	3993
rs749335372	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541483	CTGAACCCCCTTGGG[A/G]CCTTGGATCAAGTGG	3993
rs749385177	snp	A/C/T			intron-variant	LLGL2	GRCh38.p7	17:75539900	AGGTGTGAGTTACTG[A/C/T]GGCTGGTTGGAAATC	3993
rs749415050	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566666	TCAGGCTGTAATTTC[C/T]TGGCCCCTTGTCTAG	3993
rs749423549	snp	A/G	0.000261755	0.0114372	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564556	AGGTGTGGGAGGCAT[A/G]GGGCAGGACCATCAG	3993
rs749462758	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75549513	ACCCAGCAGCCCCTG[A/C]GGAGGGCCAGGTTGT	3993
rs749478316	snp	C/G	1.68187e-05	0.00289984	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563067	GATGGTGGAGGCACT[C/G]CAGGAGCACCCTCGA	3993
rs749491159	snp	C/G	1.70953e-05	0.00292359	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572011	GATCTGTCGAAGAGC[C/G]CTGACATGCAGGGAA	3993
rs749605554	in-del	-/G	1.68388e-05	0.00290158	intron-variant	LLGL2	GRCh38.p7	17:75569155	GGAGCCTGGGACCCA[-/G]GGAAGGGCAGAGGCC	3993
rs749619974	snp	C/T	0.000811077	0.0201216	intron-variant	LLGL2	GRCh38.p7	17:75558508	CGTCGTGTGCCCTCG[C/T]CAGTGCCAGCTGGTC	3993
rs749621586	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572238	GAGGACACTGAGGCA[A/G]GACAGGGGGCCAGGC	3993
rs749665958	snp	C/T	1.92066e-05	0.00309886	intron-variant	LLGL2	GRCh38.p7	17:75568889	GTAGGATATGTGGGG[C/T]GGGAGCAGAGCCCTG	3993
rs749672238	snp	A/G	1.68179e-05	0.00289977	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573134	GCCGAGGACTACGGG[A/G]AGCACCACCTGGCAG	3993
rs749704053	snp	A/G	1.69499e-05	0.00291112	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563391	AGCTGTCACTCTGAC[A/G]GCAGCTACTGCCAGT	3993
rs749734318	snp	C/T	3.32132e-05	0.00407499	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543463	GGGCATGACCCTGTG[C/T]GGGAGAGGCTCAAGC	3993
rs749800942	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75570626	TTCAGGGTCCAGGTC[A/G]CATTGTGTGACCTCA	3993
rs749804539	in-del	-/T	1.73552e-05	0.00294573	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573592	GAACCACCGCCCTGG[-/T]TAACGGTGCGGGCCC	3993
rs749835566	snp	A/G	1.66621e-05	0.00288631	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569291	TCCTCTGCAAGTACA[A/G]CGGCTACCTGGCTGT	3993
rs749986955	snp	C/T	3.40188e-05	0.00412411	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571991	AGCCCCTCGAAGTGG[C/T]CCATGATCTGTCGAA	3993
rs749996510	snp	A/G	1.64789e-05	0.0028704	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524211	TCTGGGAGCCCTAGA[A/G]CTTAGGAGTGGGCTA	3993
rs750018830	snp	C/T	8.25812e-05	0.00642524	utr-variant-3-prime, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574899	TGAGCGTCCAGGCTG[C/T]GCGATGAGCACACAC	3993
rs750020285	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75531248	GGAAGACGAAGTGCT[A/G]CCTGGGACCAGGTGG	3993
rs750043640	snp	A/G	3.51352e-05	0.00419122	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569069	CGCGTGTTCCTCACC[A/G]ACACGGACCCCAACG	3993
rs750048313	snp	C/T	1.65146e-05	0.0028735	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558179	CCCAGGCGTGGAGTT[C/T]ATGGGGCTGCACCAG	3993
rs750085949	snp	A/G	1.65548e-05	0.002877	intron-variant	LLGL2	GRCh38.p7	17:75558113	CAAGGCAGGCAGGGG[A/G]TGGTGTCCGACCTTC	3993
rs750103273	snp	A/G	8.12612e-05	0.00637369	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570468	CCGGGTGTCCAGCCG[A/G]AAGCGGCACCCGGCT	3993
rs750128987	in-del	-/C	1.97035e-05	0.00313868	intron-variant	LLGL2	GRCh38.p7	17:75572090	GGCAGCGGCGGGTCT[-/C]CCTGGGACTCCCCGG	3993
rs750182152	in-del	-/TC	3.30469e-05	0.00406477	intron-variant	LLGL2	GRCh38.p7	17:75574827	GGCTGGGGCACCCCG[-/TC]TCCTGCCCAGGGTGA	3993
rs750198384	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542195	TGGTTAATTTTTGCC[A/T]CCTCCCAAGAACGCG	3993
rs750218388	in-del	-/AA/AAA			intron-variant	LLGL2	GRCh38.p7	17:75527167	GTGAGACCCTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	3993
rs750227574	snp	A/G	1.67905e-05	0.00289741	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543416	CCAGTGGGGGCTGCA[A/G]ACTAAGCAAAATGAG	3993
rs750227627	snp	A/G	5.83311e-05	0.0054002	intron-variant	LLGL2	GRCh38.p7	17:75558655	TCCCCAGCCCCTTCC[A/G]CTCCCAGCCCAGCCT	3993
rs750241847	snp	A/G	0.000415707	0.0144111	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568668	TTGCCGCCGGCAGCC[A/G]GCAGAACGCACACTT	3993
rs750289860	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75552364	CGTGGTGGTGTGTGC[C/T]TGTAGTCCCAGCTCC	3993
rs750303771	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75530148	CTTTTGGAAGTGCCT[G/T]ATGGGTTTAGGGAAT	3993
rs750317285	snp	G/T	3.35194e-05	0.00409372	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568548	ACCTGCAGACAGCAG[G/T]CTGGCCACCGGTCCA	3993
rs750370173	snp	C/T	3.79427e-05	0.00435545	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568452	CTCCTGGCCCCGGCC[C/T]CTGACCCTTGCCCTG	3993
rs750385877	snp	A/G	1.64963e-05	0.00287192	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569982	TGGTACTGGAACTGA[A/G]TGACGAGGCAGCGGA	3993
rs750389915	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558702	TCTGGAGTGGACTCA[C/T]CCTTTGTGAGGCCTG	3993
rs750399789	snp	C/T	0.00205834	0.0320146	intron-variant	LLGL2	GRCh38.p7	17:75573674	CGCCCCTCCCGCCCC[C/T]CCCTGCCCTCTCTGA	3993
rs750456928	snp	C/G/T	9.66417e-05	0.00695065	missense, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574491	ACACTGGAGGGAGAC[C/G/T]GCGGGTGAGGCACCG	3993
rs750483709	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75574020	GCACACCTGGGCCAC[A/T]CCCGGCCCAGACCTG	3993
rs750490407	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566240	AGCCGTGGAGGCACG[C/G]TAAGGACTTGGGGTT	3993
rs750507402	snp	C/T	3.88327e-05	0.00440623	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570187	CTCTGAGTGGCGGCT[C/T]GTGGCCTTCGGCACC	3993
rs750509714	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75544546	ATAGAAGCTGGATGG[C/T]CGTGTGCCTGTCGCC	3993
rs750514591	snp	C/T	0.000143284	0.00846293	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570095	CGCTCAGGGCCCGTG[C/T]GCTTTGAGCCTGGCT	3993
rs750531277	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75546154	GTGTGCAGGATGACC[A/G]TGAAGTCTCTGACCT	3993
rs750543311	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567903	CCGAGATCACACCAC[C/T]GTACTCCAGCCTGGG	3993
rs750592759	snp	G/T	1.6477e-05	0.00287024	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523376	TGCAGTACCTTGACC[G/T]CCAGGAGTTGGTGGT	3993
rs750599701	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534074	CTGGATGGCCTGCCC[A/G]CGCCAGCCCCAGGCA	3993
rs750632310	snp	C/G	1.70124e-05	0.00291649	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563363	GTGGCAGCGGGACGG[C/G]CGCCTGCTCGTCAGC	3993
rs750662990	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75537067	ACCTCAAGTGATCCA[C/G]CCGCCTCGGCCTCCC	3993
rs750670381	snp	C/G	1.6863e-05	0.00290365	intron-variant	LLGL2	GRCh38.p7	17:75568724	GCCCCAGCCCCAGCC[C/G]CACCGCAAGCCAAAC	3993
rs750699921	snp	C/T	1.93339e-05	0.00310912	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574601	ACTCCCCTGTCTTTG[C/T]CTGTGCAGGAGCGGC	3993
rs750712674	snp	A/C	1.64732e-05	0.0028699	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523292	GTGGTCCTTCAGCAT[A/C]TCTCTGTGCTGCAGA	3993
rs750724002	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566188	GGCAGAATGGCCCCC[A/G]TGCTGGTCCAGATGT	3993
rs750731297	snp	C/T	0.000120979	0.00777654	intron-variant	LLGL2	GRCh38.p7	17:75573443	GGCAGCCTTGGCAGC[C/T]GCCAGGCCAGGCCGC	3993
rs750743324	in-del	-/ACACACACACACAC/ACACACACACACACACAC			intron-variant	LLGL2	GRCh38.p7	17:75532053	TATATATATGTATAT[lengthTooLong]ATACACACACACACA	3993
rs750763517	in-del	-/CTC			intron-variant	LLGL2	GRCh38.p7	17:75529226	TCTTTGAGACGAAGT[-/CTC]CTCTGTCGCCCAGGA	3993
rs750766232	snp	C/T	1.656e-05	0.00287745	intron-variant	LLGL2	GRCh38.p7	17:75563833	TGCTGGTCCTCTTTC[C/T]TCTCCAGAGCCTTCC	3993
rs750809505	snp	C/T	1.64743e-05	0.00287	upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524326	CAGAGTGGGGATGTC[C/T]CTCTGATCTTTGCCC	3993
rs750818724	in-del	-/CG			intron-variant	LLGL2	GRCh38.p7	17:75550068	CTGGATGCCGCGCTT[-/CG]GAGGCCCCAGTGGCT	3993
rs750838870	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75535573	AAGCCTTGGTCTCAC[A/G]GGGACAAATTAGCCC	3993
rs750849672	snp	A/G	1.80543e-05	0.00300447	intron-variant	LLGL2	GRCh38.p7	17:75573281	AAATATGGCCAAGGT[A/G]TTTGAGCCGGGCTGG	3993
rs750895267	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75565283	GGGCTGATGTTGAAA[A/C]CTGGAGAGGAGCCCT	3993
rs750945305	snp	C/T	1.66863e-05	0.0028884	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564405	GCCAGCTACGGGGAC[C/T]GCCACTGCATCTCAG	3993
rs750985663	in-del	-/G			intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574282	TGGGTGGGAGAGGGT[-/G]GGGCTGGCAGGAGGG	3993
rs751007686	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75537487	TCACTTGAGATCAGG[A/G]GTTCGAGACCAGCCT	3993
rs751086102	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75546051	GGTAAAATCGCTCCT[G/T]GTTTGAGACCCATGG	3993
rs751107332	snp	A/G	3.48535e-05	0.00417439	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569082	CCGACACGGACCCCA[A/G]CGAGAACTTCAGTGC	3993
rs751109863	snp	C/T	5.2044e-05	0.00510091	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573021	GCCCCCAGGTGTTCA[C/T]GCTGCCCAAGGTGAG	3993
rs751128543	snp	A/G	1.70055e-05	0.0029159	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570474	GTCCAGCCGGAAGCG[A/G]CACCCGGCTGGCCCC	3993
rs751163040	snp	C/G	1.65303e-05	0.00287487	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524448	TGGAGCTTGCTCCGG[C/G]GGACCGGGACTGTCT	3993
rs751178420	snp	A/G	3.39345e-05	0.00411899	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569131	GCCCCCACTCCGCAA[A/G]GTGAGGCCAGGAGCC	3993
rs751196444	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75530120	TCCCAGGCCTTTGGG[G/T]GGGCACTTGGGCCTT	3993
rs751211410	snp	C/T			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568445	CTGCTTCCTCCTGGC[C/T]CCGGCCCCTGACCCT	3993
rs751211598	snp	A/C	1.66502e-05	0.00288527	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564426	TGCATCTCAGTGATC[A/C]ACGATGGCCAGCAGA	3993
rs751297835	snp	C/T	0.000130899	0.00808902	intron-variant	LLGL2	GRCh38.p7	17:75574090	TGTTTGGGCTGGGAA[C/T]AGAGACGGCATTCCT	3993
rs751311283	snp	C/G	3.3461e-05	0.00409016	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568561	AGGCTGGCCACCGGT[C/G]CAGCTGCCCTACCTG	3993
rs751323278	snp	A/G	1.7139e-05	0.00292732	intron-variant	LLGL2	GRCh38.p7	17:75556009	TGGCGCGAAGGGGAC[A/G]GGTCTGCAGGCCCAC	3993
rs751424518	snp	A/C/G	8.38654e-05	0.0064751	intron-variant	LLGL2	GRCh38.p7	17:75573679	CTCCCGCCCCTCCCT[A/C/G]CCCTCTCTGAGATAC	3993
rs751437045	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75541113	CTCCTGATGCCATTG[C/T]TACACCCTGTCTTCC	3993
rs751457037	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75550081	TTCGGAGGCCCCAGT[C/G]GCTGCCAGGCAGCTT	3993
rs751459220	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75562775	GGGTTTTGCCATGTT[A/G]GCCAGGCTGCTCTCA	3993
rs751545849	snp	A/C	1.97673e-05	0.00314377	intron-variant	LLGL2	GRCh38.p7	17:75572092	CAGCGGCGGGTCTCC[A/C]TGGGACTCCCCGGGA	3993
rs751558406	snp	C/G	1.69965e-05	0.00291513	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563369	GCGGGACGGCCGCCT[C/G]CTCGTCAGCTGTCAC	3993
rs751634917	snp	G/T	1.68281e-05	0.00290065	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573125	AGTCGTCGAGCCGAG[G/T]ACTACGGGGAGCACC	3993
rs751639897	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75571222	GAGGTTTCCCCTTGT[A/G]AGCAGGGGCAGACTG	3993
rs751656735	snp	C/T	1.85606e-05	0.0030463	intron-variant	LLGL2	GRCh38.p7	17:75568848	TCACAGGGTAGGGTA[C/T]TTTGATGCTACCCCA	3993
rs751662387	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528901	AGGTGGCTTATGCCT[A/G]TAATCCCAACACTTT	3993
rs751663679	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543213	TCAGCCCTGAGGTGG[A/G]CCGGCCTCTAGATCT	3993
rs751728025	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75531484	TTTGAGCAGCACTGG[A/C]AGCCTGGACTCATTT	3993
rs751759737	snp	A/G	1.86149e-05	0.00305075	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574615	GCCTGTGCAGGAGCG[A/G]CAACTGGCGTTCACA	3993
rs751821358	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529945	CTCGTTCTTTGCCGA[A/G]TCCTTGCTGTGTGAC	3993
rs751824117	snp	C/T	8.44645e-05	0.00649808	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563453	GCCCCTCCGCAGCCT[C/T]GTGCCTTACGGTCAG	3993
rs751836174	snp	A/G	5.13132e-05	0.00506497	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570978	GTGCCAAGGCTGAGC[A/G]GCCAGGCCTCCAGAA	3993
rs751869515	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75557442	TCTGGCCGACTGGGG[-/G]CTCCCAGTGTTTTCA	3993
rs751879246	in-del	-/C			upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525191	GGGCGCCCCCCCGCA[-/C]CCCCCCCCCGAGGAA	3993
rs751886332	snp	A/G			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565121	TTTAACACCCACCCC[A/G]CTGAGGCAAGAGGGT	3993
rs751907418	snp	A/G/T	6.88615e-05	0.00586742	intron-variant	LLGL2	GRCh38.p7	17:75571822	GAGGGTGCTCGGGCT[A/G/T]CCTGGGCTGGGTCCA	3993
rs751944797	snp	A/C	1.67728e-05	0.00289588	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559374	CTTTTCGTGCGCTGG[A/C]GGACCGGACCATCAG	3993
rs751950610	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75537684	CCTGGGCGACAGAGC[A/G]AGACTCCATCTCCAA	3993
rs751960334	snp	A/C	1.69023e-05	0.00290704	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571753	CCTCCCGCCGAGCGG[A/C]GAATGGATGAGCCTG	3993
rs751971812	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75563981	ACGTCTCTCAGCGGC[A/C]CAATTCCTGCCAAGT	3993
rs751995804	snp	C/T	1.69312e-05	0.00290952	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573520	AGTTTGAGCGCTTCT[C/T]TCTCTCCACCAAGTG	3993
rs752012484	snp	C/T	0.000132015	0.00812343	intron-variant	LLGL2	GRCh38.p7	17:75570297	GCTGGGAGTGGGGCC[C/T]GCGAGGACTCCCAGG	3993
rs752021198	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75568715	CTGGCCCTGGCCCCA[A/G]CCCCAGCCCCACCGC	3993
rs752081910	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536470	ACCTGCCTGTCTCCC[C/T]GCCTTTCCGGGCCTA	3993
rs752148018	snp	G/T	1.66139e-05	0.00288213	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569221	CCTCCCCTTCTCCAG[G/T]TGGGCTCCTTTGACC	3993
rs752154844	snp	A/C	5.01559e-05	0.00500754	stop-gained, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556090	CAGCGCCCTCGGCTA[A/C]AGCCCGTCCCTGCGC	3993
rs752160702	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575195	AGTTTTTAATAAACA[C/T]CTATTACCTCTTGAC	3993
rs752188342	snp	G/T	0.000310163	0.0124493	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573541	CCACCAAGTGGCTGG[G/T]GGAGCCCCGGTGTCT	3993
rs752218773	snp	A/G	1.66899e-05	0.00288871	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524471	GACTGTCTGTTCTCA[A/G]GGACCATCTCGGCTG	3993
rs752248810	snp	A/G	1.6643e-05	0.00288465	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564436	TGATCCACGATGGCC[A/G]GCAGACGGCCTTCGA	3993
rs752300104	snp	C/G	1.6898e-05	0.00290667	intron-variant	LLGL2	GRCh38.p7	17:75569146	GGTGAGGCCAGGAGC[C/G]TGGGACCCAGGAAGG	3993
rs752311543	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75540656	TCCTTTGTTCTGTAT[A/T]ATCCATCCATCACTG	3993
rs752315745	snp	C/T	1.77084e-05	0.00297554	intron-variant	LLGL2	GRCh38.p7	17:75571849	TCCAGGGAGTGGCTC[C/T]AGCCCTGCCACCCCC	3993
rs752327661	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539545	CACCGTGCCCAGCCC[A/G]TCTCTTTTTTTTGAT	3993
rs752329596	snp	A/G	1.7708e-05	0.00297552	intron-variant	LLGL2	GRCh38.p7	17:75559433	CAGAGCCCAGCTGCT[A/G]TTAACTCCATCCCCT	3993
rs752342168	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536092	AGGGCAGAACAGGGA[A/G]GGTGGCTCAGAGGCT	3993
rs752414760	snp	A/C	0.000315756	0.012561	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524608	TGCCTTGCAGTGACC[A/C]CTCTGGAACTCAGGA	3993
rs752433356	snp	C/T	1.69046e-05	0.00290723	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573040	GCCCAAGGTGAGTGC[C/T]AAGCTGAAGTTGAAG	3993
rs752444325	snp	C/G	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523263	AGTACCTTGTTTTCT[C/G]TGTCCTTGTAGCCGT	3993
rs752499777	snp	A/G	0.000109248	0.00738999	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574444	CCTCTGTTCCCACCC[A/G]GCCTGCAGGAGTCCT	3993
rs752514219	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75532577	TACAGGTATGCGCCA[C/G]CACACCTGGCTAATT	3993
rs752556023	snp	A/G	2.20816e-05	0.0033227	intron-variant	LLGL2	GRCh38.p7	17:75572115	CCCCGGGACATCCAG[A/G]AGGCTCGGACCTTGG	3993
rs752588634	snp	C/T	1.64754e-05	0.00287009	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524367	TGGTGACATCTCCTT[C/T]TACAGCTTCAGGGAC	3993
rs752641252	snp	C/T	1.6912e-05	0.00290787	intron-variant	LLGL2	GRCh38.p7	17:75558280	CACTTCCATGCCCTC[C/T]TTGCCTTCACTGCTT	3993
rs752710584	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75533926	AAATAAAATTCCAGT[C/T]CCTCCCATGAGGCAC	3993
rs752725884	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523110	CTTGAACCTGGGAGG[C/T]AGAGGTCACAGTGAG	3993
rs752737453	snp	C/T	3.40872e-05	0.00412825	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563355	AACATCTGGTGGCAG[C/T]GGGACGGCCGCCTGC	3993
rs752743945	snp	A/C	3.30961e-05	0.0040678	intron-variant	LLGL2	GRCh38.p7	17:75563722	TCTGAGAGTTTGAGG[A/C]TCCGTTCAAGCCGAT	3993
rs752768715	snp	C/G	1.74876e-05	0.00295694	intron-variant	LLGL2	GRCh38.p7	17:75571118	GAGTGGCCAGCCTGG[C/G]GTTGGGGGGCAGGGG	3993
rs752785397	in-del	-/TTTTT			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541716	GGGATGTGGCTCTGC[-/TTTTT]TTTTTTTTTTTTTTT	3993
rs752794492	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552463	CACTGCACTCCAGGC[A/G]TGACAGGCGTGACCC	3993
rs752802240	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523857	GGACTCCTCTGTACT[C/T]CCCTGGCCAGCGTGC	3993
rs752820818	snp	A/G	1.7703e-05	0.0029751	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559283	ACACAGATCACCGTG[A/G]TCCTGCCACATTCCT	3993
rs752882431	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542397	TGCTTCCTTCCCCCA[C/T]CCTGCTGGGAGTGGA	3993
rs752902847	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536349	GCACAGCACCTGAGA[A/G]TTTGCCAAGCCCGCT	3993
rs752916177	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75563968	GTAGACGCTATTCAC[A/G]TCTCTCAGCGGCCCA	3993
rs752925091	snp	C/G	3.51179e-05	0.00419019	intron-variant	LLGL2	GRCh38.p7	17:75543545	CCCCAGGTTTTCGGC[C/G]AAGCAGCTCAGGCTG	3993
rs753041664	snp	C/T	1.83256e-05	0.00302696	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574627	GCGGCAACTGGCGTT[C/T]ACATCGAGCCGCCGT	3993
rs753045362	snp	C/T	0.000156223	0.00883669	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570218	AGCCATGGCTTTGGC[C/T]TCTTTGACCACCAGC	3993
rs753067806	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75535545	CAGGCCAGAGGGCTG[G/T]CTGGGCTTGGCCAAG	3993
rs753094004	snp	C/G			intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574289	GAGAGGGTGGGGCTG[C/G]CAGGAGGGGTGGGGA	3993
rs753094398	snp	C/T	1.65899e-05	0.00288005	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523732	CGCTGTGGCCACATT[C/T]CGAAAGAATAACCCT	3993
rs753112463	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575017	CCACAATGCAGCTGC[C/T]CTGGGCCTCGGGAGA	3993
rs753146313	snp	C/T	1.71634e-05	0.0029294	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571921	ATCCAGCTGATGCAC[C/T]GGGCGCCGGTGGTGG	3993
rs753151934	snp	C/G	4.49913e-05	0.00474275	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570393	CTTGGAGGGCCCACT[C/G]TCCCGCGTCAAGTCC	3993
rs753156877	snp	A/G	0.000135275	0.00822308	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563463	AGCCTCGTGCCTTAC[A/G]GTCAGTGTTTCACCC	3993
rs753167036	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557208	TTTTAACCTATCTCG[A/G]TAAGAATCAGAGGTG	3993
rs753168057	snp	A/G	3.54748e-05	0.00421143	splice-donor-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574669	TCAGCAATGGCGGAG[A/G]TGGGGGCTCTGGGCT	3993
rs753204767	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75546876	GCAGGTCCAGCGGAC[A/G]GTGGGATACCCAGGG	3993
rs753284940	snp	G/T	3.29636e-05	0.00405964	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523636	GGAGAAGAGTTCATG[G/T]CATAACGTTTCTCAT	3993
rs753296195	snp	A/G	0.000166449	0.00912124	intron-variant	LLGL2	GRCh38.p7	17:75558003	CTGTGTCTCCTCCCC[A/G]CCCTAGGCTCCATGC	3993
rs753344667	snp	C/T	1.71258e-05	0.00292619	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571925	AGCTGATGCACCGGG[C/T]GCCGGTGGTGGGCAT	3993
rs753351313	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566292	GCAGGGGTGCCATGA[C/T]CTAGCCTCTGCTCCA	3993
rs753356736	snp	C/T	0.000758437	0.0194588	intron-variant	LLGL2	GRCh38.p7	17:75559460	CCCTCAAGTTAGGCA[C/T]GGCTTCTCCCCTTGG	3993
rs753372108	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537894	ATTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA	3993
rs753379669	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75538366	GCATTGGGCCCCCCA[C/G]TTGTCTTCATCCTGA	3993
rs753394798	snp	C/T	2.17867e-05	0.00330044	intron-variant	LLGL2	GRCh38.p7	17:75558018	ACCCTAGGCTCCATG[C/T]ATGGGTCCTGCTGCC	3993
rs753463266	snp	C/G	0.00214765	0.0326988	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573615	GCGGGCCCCAAGAAG[C/G]CCCCGAGCCGAGCCA	3993
rs753490919	snp	A/C	1.71064e-05	0.00292454	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563035	CCAGAGGAGGCCCGC[A/C]ACCGGCGTGTGTTCG	3993
rs753580126	snp	A/G	1.69928e-05	0.00291481	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571987	CCCGAGCCCCTCGAA[A/G]TGGCCCATGATCTGT	3993
rs753605007	in-del	-/CATTGACTTTTCCAGAAGTCACTGCCTT	1.68442e-05	0.00290204	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563170	TCTACCACTTCCTCA[-/CATTGACTTTTCCAGAAGTCACTGCCTT]GCAGCCAGGTAGGCA	3993
rs753620321	snp	A/G	6.7382e-05	0.00580401	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573117	ACTTCGGCAGTCGTC[A/G]AGCCGAGGACTACGG	3993
rs753658973	snp	A/C/G/T	5.02444e-05	0.00501199	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571031	CGCAAGATCGAGGCT[A/C/G/T]GCTCGGCAGAGGACT	3993
rs753674832	snp	C/T	1.70095e-05	0.00291625	intron-variant	LLGL2	GRCh38.p7	17:75558288	TGCCCTCCTTGCCTT[C/T]ACTGCTTCCAGCAGG	3993
rs753677712	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560406	CTCACCCTGTAGTTA[A/G]CTGGCGGGAATCTAG	3993
rs753705621	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526241	GGCGGCGGCCGGAGC[G/T]CGGTGCCCCGGCGGC	3993
rs753722991	snp	C/G	3.4118e-05	0.00413012	intron-variant	LLGL2	GRCh38.p7	17:75569338	CAGGTAGCAGGCTGG[C/G]CTGGGGAGGGGGAGC	3993
rs753763623	snp	G/T	1.68889e-05	0.00290588	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543406	CTCCAGGTCTCCAGT[G/T]GGGGCTGCAGACTAA	3993
rs753764153	snp	A/G	1.70933e-05	0.00292341	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524483	TCAGGGACCATCTCG[A/G]CTGCCTCCTGTACCC	3993
rs753768242	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75569908	ACTAGTAGCATCCTG[C/T]GGCCCTGCCGTCCCT	3993
rs753776359	snp	C/T	1.65932e-05	0.00288034	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569237	TGGGCTCCTTTGACC[C/T]CTACAGTGATGACCC	3993
rs753798391	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531453	AGACCAATGTTCTTT[C/T]TCCTGGGCCGGCTGC	3993
rs753850238	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528241	CTGCCTCGGCCTCCC[A/G]AGTAGCTGGGACCAC	3993
rs753902766	snp	C/T	3.45334e-05	0.00415518	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559292	ACCGTGGTCCTGCCA[C/T]ATTCCTCCTGCGAGC	3993
rs753929368	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75551135	CTGTCCAGGTAGAGT[C/G]GCTGTGAAGGTCACT	3993
rs753959131	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75530651	CGAGACTCCATTTCA[-/A]AAAAAAAAAAAAAAA	3993
rs753962109	in-del	-/GC			intron-variant	LLGL2	GRCh38.p7	17:75535243	AAACAGGAGGCCACA[-/GC]GCCACACTCAGGCCT	3993
rs753987729	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75563578	AAAGGCTTTGTCCAA[A/C]GCCACACAGCAGGGT	3993
rs754027171	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75545884	CAACTTCAGCACTCA[C/T]AGATGATATTTGAGG	3993
rs754117890	snp	C/T	1.66907e-05	0.00288879	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568579	GCTGCCCTACCTGGC[C/T]TCTCTGCACTGTTCC	3993
rs754131023	snp	A/C	1.6513e-05	0.00287336	intron-variant	LLGL2	GRCh38.p7	17:75574854	GTGATCTTGAGCTGT[A/C]CCTCTGTGTCCTTCA	3993
rs754131418	snp	C/T	1.68995e-05	0.00290679	intron-variant	LLGL2	GRCh38.p7	17:75556029	TGCAGGCCCACCCCA[C/T]GTGCTTCTCGTTGCA	3993
rs754137470	snp	C/T			intron-variant, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574181	CGAGGAGGGCCCAGG[C/T]GGGGCGCCCTGACCC	3993
rs754162202	snp	A/G	3.39271e-05	0.00411854	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573225	GCTACAGCTGCATCC[A/G]CCGGGAGGACGTCAG	3993
rs754245908	snp	C/G	3.31835e-05	0.00407316	intron-variant	LLGL2	GRCh38.p7	17:75558103	GCCTGGCACTCAAGG[C/G]AGGCAGGGGATGGTG	3993
rs754257725	snp	A/G	1.7777e-05	0.0029813	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574674	AATGGCGGAGGTGGG[A/G]GCTCTGGGCTTGAGT	3993
rs754269155	snp	A/C	1.66454e-05	0.00288486	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523740	CCACATTCCGAAAGA[A/C]TAACCCTGGCAAACC	3993
rs754277731	snp	A/C	2.4384e-05	0.00349162	intron-variant	LLGL2	GRCh38.p7	17:75559211	ATGGCATCTCCCCTG[A/C]TGGGCAGTGGTCGGC	3993
rs754292464	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75554569	AGGCTACAGTGAACC[G/T]AAATCATGCCGTAGC	3993
rs754313550	snp	C/T	0.000105831	0.00727354	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569056	ACTCAGCACTGTGCG[C/T]GTGTTCCTCACCGAC	3993
rs754321787	snp	C/G/T	3.54222e-05	0.00420834	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573264	CCTCCTGCGTCTTCA[C/G/T]CAAATATGGCCAAGG	3993
rs754331927	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528852	AAACATTGTAGAAAG[C/T]GTAAAATTAGAGAGC	3993
rs754355635	snp	A/C	1.65405e-05	0.00287576	intron-variant	LLGL2	GRCh38.p7	17:75563730	TTTGAGGATCCGTTC[A/C]AGCCGATTCCTTTCC	3993
rs754461779	snp	A/C	0.000329457	0.0128304	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524361	GGATCATGGTGACAT[A/C]TCCTTCTACAGCTTC	3993
rs754467330	snp	C/T	3.88855e-05	0.00440922	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523806	GCCAGCACTGCCCCT[C/T]CCCCAGCTGCTGCCA	3993
rs754499317	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75527289	GGGATTTGGGGTTTA[C/G]TTTTCTTAGGCGATC	3993
rs754524882	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539381	TTTCAAAATTTTTAT[C/T]GTTCCATGTAAATTT	3993
rs754583589	snp	C/G	1.69327e-05	0.00290965	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573524	TGAGCGCTTCTCTCT[C/G]TCCACCAAGTGGCTG	3993
rs754652204	snp	C/T	1.69043e-05	0.00290721	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571757	CCGCCGAGCGGAGAA[C/T]GGATGAGCCTGTGCG	3993
rs754659748	snp	C/T	1.6797e-05	0.00289797	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559317	GCGAGCTGCTCTACC[C/T]GGGCACCGAGAGTGG	3993
rs754709487	snp	A/G	8.58671e-05	0.00655181	intron-variant	LLGL2	GRCh38.p7	17:75573457	CCGCCAGGCCAGGCC[A/G]CTAGCATTGCCCCCA	3993
rs754737971	snp	A/G	6.71344e-05	0.00579333	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563122	TACAGCCGAGGCCTC[A/G]TTGTCATCTGGGACC	3993
rs754751986	snp	C/T	2.83958e-05	0.0037679	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570434	CCTTGCGTCAGTCAT[C/T]CCGCCGGATGCGTCG	3993
rs754828795	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75549095	TGGCTGTGTGGCCTT[-/A]AGAGTGGTGGCTTCA	3993
rs754864450	snp	C/T	1.67147e-05	0.00289086	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568570	ACCGGTCCAGCTGCC[C/T]TACCTGGCTTCTCTG	3993
rs754867865	snp	C/T	4.94157e-05	0.00497045	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570479	GCCGGAAGCGGCACC[C/T]GGCTGGCCCCCCAGG	3993
rs754909041	snp	G/T	4.95544e-05	0.00497742	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574907	CAGGCTGCGCGATGA[G/T]CACACACTACTACTG	3993
rs754925688	snp	C/T			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571035	AGATCGAGGCTCGCT[C/T]GGCAGAGGACTCCTT	3993
rs754950482	snp	A/G	6.75927e-05	0.00581307	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563454	CCCCTCCGCAGCCTC[A/G]TGCCTTACGGTCAGT	3993
rs754974940	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549323	TCCTAGACAACTGCT[C/T]ACAGCCAGCTCGCTC	3993
rs755011174	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528968	TCGAGACTAGCCTTG[C/T]CCACACAGTGAAACC	3993
rs755059061	snp	C/T	0.000135247	0.00822224	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570988	TGAGCGGCCAGGCCT[C/T]CAGAACATGGAGCTG	3993
rs755072570	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75541231	GCCCTCTTGTCCCCT[C/T]CCTGGAGTCTGCAGG	3993
rs755109072	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75552372	TGTGTGCCTGTAGTC[C/T]CAGCTCCTCAGGAGG	3993
rs755111571	snp	C/T	1.85741e-05	0.00304741	intron-variant	LLGL2	GRCh38.p7	17:75568849	CACAGGGTAGGGTAC[C/T]TTGATGCTACCCCAC	3993
rs755124108	snp	C/T	6.63548e-05	0.0057596	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569252	CCTACAGTGATGACC[C/T]CCGGCTGGGCATCCA	3993
rs755137695	in-del	-/TTT			intron-variant	LLGL2	GRCh38.p7	17:75555292	GGTAATTTTTGTTCT[-/TTT]TTTTTTTTTTTTTGA	3993
rs755139483	snp	G/T	6.59261e-05	0.00574097	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523622	AAAAGAAAGGTTGGG[G/T]AGAAGAGTTCATGTC	3993
rs755149481	snp	C/T	1.69876e-05	0.00291436	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563370	CGGGACGGCCGCCTG[C/T]TCGTCAGCTGTCACT	3993
rs755165090	in-del	-/AAAC			intron-variant	LLGL2	GRCh38.p7	17:75528740	CAAAACTCCATCTCA[-/AAAC]AAACAAACAAACAAA	3993
rs755194875	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562394	CCTCCGGAGGTCTTA[C/T]GCACCCTTCCTAGTC	3993
rs755211863	snp	C/G/T	5.07664e-05	0.00503796	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563049	CCACCGGCGTGTGTT[C/G/T]GAGATGGTGGAGGCA	3993
rs755244871	snp	A/C	3.335e-05	0.00408337	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556094	GCCCTCGGCTACAGC[A/C]CGTCCCTGCGCATCC	3993
rs755343443	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75572499	AAACCCCGTCTCTAC[A/T]AACAAATGCAAAAAA	3993
rs755348646	snp	A/G	2.95207e-05	0.00384181	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570128	CAGCCCTTCGTGTTG[A/G]TGCAGTGTCAGCCCC	3993
rs755405219	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534216	CCCCAGAATGGGGGT[A/G]CGTTCCCACCTTCCA	3993
rs755443265	snp	C/T	1.64732e-05	0.0028699	stop-gained, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523304	CATATCTCTGTGCTG[C/T]AGACAACACACCTTC	3993
rs755452752	snp	A/C/G	5.07184e-05	0.00503558	intron-variant	LLGL2	GRCh38.p7	17:75568732	CCCAGCCCCACCGCA[A/C/G]GCCAAACTCTCCCAT	3993
rs755544035	snp	C/T	5.01442e-05	0.00500695	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556065	TGGAGCATGGCTTCC[C/T]GCACCAGCCCAGCGC	3993
rs755585740	snp	A/G	9.37778e-05	0.00684691	missense, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574495	TGGAGGGAGACCGCG[A/G]GTGAGGCACCGCCCA	3993
rs755593907	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536530	CCCCACTCAGGTTGC[A/G]GTGGCTGGAGAGGAG	3993
rs755617927	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75537697	CGAGACTCCATCTCC[-/A]AAAAAAAAAAAATCC	3993
rs755644011	snp	G/T	1.68462e-05	0.00290221	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559381	TGCGCTGGAGGACCG[G/T]ACCATCAGCTCGGAC	3993
rs755683728	snp	A/G			upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524971	TCCCGAAGGGAGGAG[A/G]GAGGACGGCGCGCCA	3993
rs755715267	snp	A/G	1.70321e-05	0.00291818	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573542	CACCAAGTGGCTGGT[A/G]GAGCCCCGGTGTCTG	3993
rs755719033	snp	A/G	1.71552e-05	0.0029287	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571922	TCCAGCTGATGCACC[A/G]GGCGCCGGTGGTGGG	3993
rs755748635	in-del	-/TTTTTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75557047	ACTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTGTG	3993
rs755787767	snp	C/T	0.000234859	0.0108339	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570236	TTTGACCACCAGCAG[C/T]GGCGGCAGGTCTTTG	3993
rs755804238	snp	A/T	1.79255e-05	0.00299373	intron-variant	LLGL2	GRCh38.p7	17:75559450	TAACTCCATCCCCTC[A/T]AGTTAGGCATGGCTT	3993
rs755823239	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75569468	GCTTGATCCCCTTGG[C/T]GGGAGGTCCCTGGGA	3993
rs755841111	snp	A/C	0.000126781	0.00796079	intron-variant	LLGL2	GRCh38.p7	17:75571850	CCAGGGAGTGGCTCC[A/C]GCCCTGCCACCCCCT	3993
rs755890200	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530222	ATTTTAAAGTCTCTG[A/G]CTGGGCATTTTGGCT	3993
rs755890954	snp	A/G	1.65611e-05	0.00287755	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558220	CTGTGACGCAGATCC[A/G]CCTCCTGCCCGGCCA	3993
rs755908532	snp	C/T	0.00012444	0.00788698	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570482	GGAAGCGGCACCCGG[C/T]TGGCCCCCCAGGAGA	3993
rs755908584	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75531267	GGGACCAGGTGGCCC[A/G]TGAGCCCCTGCCCGC	3993
rs755943993	snp	A/G/T	8.39404e-05	0.00647796	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573058	GCTGAAGTTGAAGCT[A/G/T]ACGGCCCTGGAGGGC	3993
rs755974967	snp	A/G	1.68795e-05	0.00290507	intron-variant	LLGL2	GRCh38.p7	17:75569149	GAGGCCAGGAGCCTG[A/G]GACCCAGGAAGGGCA	3993
rs756039105	snp	A/C	1.71687e-05	0.00292986	intron-variant	LLGL2	GRCh38.p7	17:75563228	TGCTCTCCCAGGGCC[A/C]CAAGTGGCACATACA	3993
rs756054089	in-del	-/A	1.77269e-05	0.0029771	intron-variant	LLGL2	GRCh38.p7	17:75559436	AGCCCAGCTGCTGTT[-/A]ACTCCATCCCCTCAA	3993
rs756057349	snp	C/G	1.70252e-05	0.00291759	intron-variant	LLGL2	GRCh38.p7	17:75573477	CATTGCCCCCACTCC[C/G]CAGGCTTCTACCTGA	3993
rs756083860	snp	G/T	3.29527e-05	0.00405898	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524375	TCTCCTTCTACAGCT[G/T]CAGGGACTTCACGTT	3993
rs756089246	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75529609	GTCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA	3993
rs756097998	snp	C/T	1.64939e-05	0.0028717	intron-variant	LLGL2	GRCh38.p7	17:75559208	TCCATGGCATCTCCC[C/T]TGCTGGGCAGTGGTC	3993
rs756101271	snp	C/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523215	GGCCGTCCTAAACTA[C/G]ATGGCAGACTGAGAA	3993
rs756121358	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75562304	AATGCACTGAATATG[A/C]ATGTACAGTTTAACA	3993
rs756169094	snp	C/G	1.66156e-05	0.00288228	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543449	GGTTCCTGAGGCCAG[C/G]GCATGACCCTGTGCG	3993
rs756206946	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75550150	AGGGTCCTAGAATAG[C/T]TGGGGAGGGCTGGTC	3993
rs756209115	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562970	TGCTGGGGGCCATTC[C/T]CCCTGGTGGACGGCA	3993
rs756215557	snp	A/G	3.45835e-05	0.00415819	intron-variant	LLGL2	GRCh38.p7	17:75569369	TGGGGAGGAGTGGTC[A/G]ATGACTGGGGACAGC	3993
rs756250484	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534109	GTCCATCTTCTCCCC[A/G]GAATGGTTTTGCTTT	3993
rs756255865	snp	C/T	1.65474e-05	0.00287636	intron-variant	LLGL2	GRCh38.p7	17:75563725	GAGAGTTTGAGGATC[C/T]GTTCAAGCCGATTCC	3993
rs756261649	snp	A/C	1.70991e-05	0.00292391	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568486	CCCAGCCTTTGACGA[A/C]CCCTATGCCCTGGTG	3993
rs756332693	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75571467	GATGACGTGTCTCTC[A/C]CTGGCTGGTTCTCCC	3993
rs756333177	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75544665	GCTGGAGGGGATCTC[A/C]GTGACCTCCCTGTTG	3993
rs756451897	snp	A/G	2.53675e-05	0.00356134	intron-variant	LLGL2	GRCh38.p7	17:75570301	GGAGTGGGGCCCGCG[A/G]GGACTCCCAGGACCT	3993
rs756488981	snp	C/T	1.72958e-05	0.00294068	intron-variant	LLGL2	GRCh38.p7	17:75568760	CATGGACTTCTTGGT[C/T]TCTTTTTCTAGGAGT	3993
rs756526176	snp	C/T	2.33976e-05	0.00342027	intron-variant	LLGL2	GRCh38.p7	17:75558013	TCCCCACCCTAGGCT[C/T]CATGCATGGGTCCTG	3993
rs756588815	in-del	-/CCA	1.69355e-05	0.00290989	cds-indel, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573526	AGCGCTTCTCTCTCT[-/CCA]CCAAGTGGCTGGTGG	3993
rs756593185	snp	A/G	1.69576e-05	0.00291179	intron-variant	LLGL2	GRCh38.p7	17:75563470	TGCCTTACGGTCAGT[A/G]TTTCACCCGCCGGGC	3993
rs756612177	snp	A/C/G/T	0.000100157	0.00707606	intron-variant	LLGL2	GRCh38.p7	17:75556161	ATCCTCCGTCCCCTC[A/C/G/T]CTCCCACTCGGGCAG	3993
rs756629369	snp	C/G	6.72857e-05	0.00579986	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573132	GAGCCGAGGACTACG[C/G]GGAGCACCACCTGGC	3993
rs756630896	snp	A/C	1.69427e-05	0.00291051	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573221	GTGCGCTACAGCTGC[A/C]TCCGCCGGGAGGACG	3993
rs756673867	snp	C/G	1.66949e-05	0.00288915	intron-variant	LLGL2	GRCh38.p7	17:75556164	CTCCGTCCCCTCGCT[C/G]CCACTCGGGCAGGGC	3993
rs756732152	snp	C/T	1.70837e-05	0.00292259	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563037	AGAGGAGGCCCGCCA[C/T]CGGCGTGTGTTCGAG	3993
rs756781916	snp	A/T	2.3214e-05	0.00340682	intron-variant	LLGL2	GRCh38.p7	17:75570317	GGACTCCCAGGACCT[A/T]GCAGCACTGACAGCC	3993
rs756782520	snp	A/C	1.65067e-05	0.00287282	intron-variant	LLGL2	GRCh38.p7	17:75562969	ATGCTGGGGGCCATT[A/C]CCCCTGGTGGACGGC	3993
rs756790984	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75535750	TGGTCTCTTTCTTGA[A/G]CTCTTGAGATGGAAG	3993
rs756825957	snp	C/T	1.9679e-05	0.00313674	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568446	TGCTTCCTCCTGGCC[C/T]CGGCCCCTGACCCTT	3993
rs756866531	in-del	-/C	3.29571e-05	0.00405924	upstream-variant-2KB, frameshift-variant, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524392	AGGGACTTCACGTTG[-/C]CCCAGGATGTGGGGC	3993
rs756904219	snp	C/T	1.9662e-05	0.00313538	intron-variant	LLGL2	GRCh38.p7	17:75568912	GAGCCCTGAGGTGGA[C/T]GAGCCAGCCCCTGGG	3993
rs756919874	in-del	-/TTCCT	1.6534e-05	0.00287519	intron-variant	LLGL2	GRCh38.p7	17:75563737	ATCCGTTCAAGCCGA[-/TTCCT]TTCCTTTCAGGTCCC	3993
rs756949213	snp	C/T	4.98824e-05	0.00499387	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568638	ACATCCCGCTGAAGC[C/T]GTGGGAGCGGATCAT	3993
rs756985863	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530131	TGGGTGGGCACTTGG[A/G]CCTTTTGGAAGTGCC	3993
rs757003953	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75557383	TTCCCCGGCCTGAGG[C/G]TGGATGTTGTCCAGT	3993
rs757032739	in-del	-/GCCCCT			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526260	TGCCCCGGCGGCTTA[-/GCCCCT]GCCCCTGCCATCTGG	3993
rs757055462	snp	G/T	1.67868e-05	0.00289709	intron-variant	LLGL2	GRCh38.p7	17:75569165	GACCCAGGAAGGGCA[G/T]AGGCCAGCTGGGTCC	3993
rs757055905	snp	A/C	3.46476e-05	0.00416204	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524487	GGACCATCTCGGCTG[A/C]CTCCTGTACCCAGAC	3993
rs757084371	snp	A/G	1.71649e-05	0.00292953	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570976	GAGTGCCAAGGCTGA[A/G]CGGCCAGGCCTCCAG	3993
rs757100101	snp	A/G	2.27705e-05	0.00337413	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558576	TGAAGGTCAAGGGCG[A/G]GGCATCGGAGCTGCA	3993
rs757175023	snp	G/T	5.05906e-05	0.00502919	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543409	CAGGTCTCCAGTGGG[G/T]GCTGCAGACTAAGCA	3993
rs757188203	snp	C/G	7.73186e-05	0.00621718	intron-variant	LLGL2	GRCh38.p7	17:75558462	CCCCAGTGTGTAAAG[C/G]CCTTGCCTGGGTAGC	3993
rs757195263	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75556488	TTTCCCCTCTCACCT[A/G]TTCCTGGAGGTTTCA	3993
rs757246505	snp	A/G	9.32379e-05	0.00682717	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570092	GCCCGCTCAGGGCCC[A/G]TGCGCTTTGAGCCTG	3993
rs757251226	snp	A/G	1.78465e-05	0.00298712	intron-variant	LLGL2	GRCh38.p7	17:75571856	AGTGGCTCCAGCCCT[A/G]CCACCCCCTCACCAG	3993
rs757256244	snp	C/T	6.82524e-05	0.00584136	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573549	TGGCTGGTGGAGCCC[C/T]GGTGTCTGGTGGATT	3993
rs757258222	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539895	ATTACAGGTGTGAGT[C/T]ACTGCGGCTGGTTGG	3993
rs757289783	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75571268	TACTCCCCTCCCCTG[C/T]CTCAGCCTCTGAGTC	3993
rs757305953	snp	A/G	6.75162e-05	0.00580978	intron-variant	LLGL2	GRCh38.p7	17:75556030	GCAGGCCCACCCCAC[A/G]TGCTTCTCGTTGCAG	3993
rs757358471	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75532616	TTTAGTAGCGGGGGG[A/G]TTTCCACCATGTTGG	3993
rs757373684	snp	C/T	1.66732e-05	0.00288727	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568589	CTGGCTTCTCTGCAC[C/T]GTTCCGCCATCACCT	3993
rs757395770	snp	C/T	3.43336e-05	0.00414314	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559296	TGGTCCTGCCACATT[C/T]CTCCTGCGAGCTGCT	3993
rs757397922	snp	A/C/G			intron-variant	LLGL2	GRCh38.p7	17:75543877	GGATGAACTCTTCAG[A/C/G]GGGTGATAATGTTCC	3993
rs757400775	in-del	-/TTTT			intron-variant	LLGL2	GRCh38.p7	17:75555291	GGGTAATTTTTGTTC[-/TTTT]TTTTTTTTTTTTTGA	3993
rs757431197	snp	A/G			intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523552	GCCCCCAACCCTCAA[A/G]TGGCACCTCTGTGAG	3993
rs757459785	snp	C/T	6.26782e-05	0.00559778	intron-variant, utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574194	GGCGGGGCGCCCTGA[C/T]CCGGCCTCTACCTTC	3993
rs757485038	snp	A/G	0.000430478	0.0146647	splice-acceptor-variant, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574452	CCCACCCGGCCTGCA[A/G]GAGTCCTGAAGGAAA	3993
rs757531435	snp	C/T	1.67815e-05	0.00289663	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563129	GAGGCCTCGTTGTCA[C/T]CTGGGACCTACAGGG	3993
rs757577689	snp	A/G			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565217	AGCTCCAGCAGGACC[A/G]GCAGAGCCCTGAGTC	3993
rs757645582	snp	A/G	1.65113e-05	0.00287322	synonymous-codon, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574877	GTCCTTCAGCAGAGT[A/G]AGTGGCTGAGCGTCC	3993
rs757668511	snp	C/T	2.1056e-05	0.00324462	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523826	AGCTGCTGCCAGTTC[C/T]CCTGTGAACCAAGTG	3993
rs757717235	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75553577	CTAAGGAGGCTGCCT[C/T]ATTGTTGGGACCTTT	3993
rs757776177	snp	A/G/T	4.84523e-05	0.00492181	intron-variant	LLGL2	GRCh38.p7	17:75559215	CATCTCCCCTGCTGG[A/G/T]CAGTGGTCGGCTCAC	3993
rs757802555	snp	A/G	1.65427e-05	0.00287595	intron-variant	LLGL2	GRCh38.p7	17:75563817	CAGGGGTAGGTATCC[A/G]TGCTGGTCCTCTTTC	3993
rs757873146	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75557231	CAGAGGTGGACTGGC[A/C]CCAGGGCCCTATCCA	3993
rs757884299	snp	C/T	9.0212e-05	0.00671549	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570472	GTGTCCAGCCGGAAG[C/T]GGCACCCGGCTGGCC	3993
rs757942135	snp	A/G	1.75265e-05	0.00296023	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568993	GCACGAGGACGGCAC[A/G]GTGCGGTTCTGGGAT	3993
rs757944023	in-del	-/C	1.68091e-05	0.00289901	intron-variant	LLGL2	GRCh38.p7	17:75568722	TGGCCCCAGCCCCAG[-/C]CCCACCGCAAGCCAA	3993
rs757960258	in-del	-/A	1.67077e-05	0.00289026	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559328	TACCTGGGCACCGAG[-/A]GTGGCAACGTGTTTG	3993
rs757974603	snp	C/T	3.35666e-05	0.00409661	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563113	CTGATCGGCTACAGC[C/T]GAGGCCTCGTTGTCA	3993
rs757991541	snp	C/G	2.55928e-05	0.00357711	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570420	GTCCCTCAAGAAGTC[C/G]TTGCGTCAGTCATTC	3993
rs758000856	in-del	-/AGG	3.64524e-05	0.00426906	intron-variant	LLGL2	GRCh38.p7	17:75572965	GCAGCAGCACAGGGC[-/AGG]AGAACTGGTTTGGCC	3993
rs758038846	in-del	-/AGCCTTGGCAGCCG	0.000141835	0.00842006	intron-variant	LLGL2	GRCh38.p7	17:75573431	CCCAGGTGGGGAGGC[-/AGCCTTGGCAGCCG]CCAGGCCAGGCCGCT	3993
rs758043668	snp	C/T	1.65266e-05	0.00287455	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563770	CCTTTCCTTGCAAAG[C/T]GATTACCAGAATCCT	3993
rs758071961	snp	G/T	1.64787e-05	0.00287038	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524223	AGAGCTTAGGAGTGG[G/T]CTATGGCTGGGTCTC	3993
rs758113032	snp	A/G	1.65173e-05	0.00287374	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574900	GAGCGTCCAGGCTGC[A/G]CGATGAGCACACACT	3993
rs758125144	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567318	AAAATAAAAAATTAG[C/G]CAGGCATTGGTGGTA	3993
rs758143484	snp	A/C	1.64792e-05	0.00287042	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568458	GCCCCGGCCCCTGAC[A/C]CTTGCCCTGTACCCC	3993
rs758173343	snp	A/G/T			intron-variant	LLGL2	GRCh38.p7	17:75528405	CAGGCGTAAGCCACC[A/G/T]CGCCCGGCCTTAAAT	3993
rs758204481	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558803	TGGGCGGGGCTGCAG[C/T]CTGCCTCCTCCATCC	3993
rs758244118	snp	C/G	1.71281e-05	0.00292639	stop-lost, intron-variant	LLGL2	GRCh38.p7	17:75564542	GGGTGCCCAGGGTTA[C/G]GTGTGGGAGGCATGG	3993
rs758248078	snp	C/T	1.78928e-05	0.002991	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573624	AAGAAGGCCCCGAGC[C/T]GAGCCAGGTGAGTGA	3993
rs758261588	snp	A/G	1.70275e-05	0.00291778	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571994	CCCTCGAAGTGGCCC[A/G]TGATCTGTCGAAGAG	3993
rs758313722	snp	C/T			synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571983	CCTTCCCGAGCCCCT[C/T]GAAGTGGCCCATGAT	3993
rs758319088	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75573677	CCCTCCCGCCCCTCC[A/C]TGCCCTCTCTGAGAT	3993
rs758332714	snp	A/G	3.33133e-05	0.00408112	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543434	TAAGCAAAATGAGGC[A/G]GTTCCTGAGGCCAGG	3993
rs758339544	snp	C/T	3.37285e-05	0.00410647	intron-variant	LLGL2	GRCh38.p7	17:75568727	CCAGCCCCAGCCCCA[C/T]CGCAAGCCAAACTCT	3993
rs758350570	snp	C/T	1.70194e-05	0.00291709	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563041	GAGGCCCGCCACCGG[C/T]GTGTGTTCGAGATGG	3993
rs758355577	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542400	TTCCTTCCCCCATCC[C/T]GCTGGGAGTGGACGG	3993
rs758400028	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75561964	TTAAAGTCCCCTTCA[A/G]CTCTCACTCTTGATT	3993
rs758407666	snp	C/G	0.000119055	0.00771448	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571944	GGTGGTGGGCATCCT[C/G]GTGCTCGACGGACAC	3993
rs758443249	snp	C/T	3.29462e-05	0.00405857	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523296	TCCTTCAGCATATCT[C/T]TGTGCTGCAGACAAC	3993
rs758470244	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75564195	ATGCCCTCACCTTAC[C/T]TCCAAGTCCTCCTGG	3993
rs758506409	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530306	CCAGGAGTTCAAGAC[C/T]AGCCTGGGCAACAGT	3993
rs758512439	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75546450	ACATGAGTTCCTGCA[C/T]GAATCGAAGGCCACG	3993
rs758542095	snp	C/G	1.89629e-05	0.00307914	intron-variant	LLGL2	GRCh38.p7	17:75570549	CCCAGGTTCGGCTCA[C/G]AGCAGCCAGCAGGGG	3993
rs758567092	snp	C/T	3.33884e-05	0.00408572	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556084	CCAGCCCAGCGCCCT[C/T]GGCTACAGCCCGTCC	3993
rs758601243	snp	C/G	1.67694e-05	0.00289558	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573067	GAAGCTGACGGCCCT[C/G]GAGGGCTCAAGAGTG	3993
rs758619318	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75552549	ACGTGTGATTAACTA[C/T]TAATGAGATTTTTTC	3993
rs758645564	snp	C/T	1.68363e-05	0.00290136	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573121	CGGCAGTCGTCGAGC[C/T]GAGGACTACGGGGAG	3993
rs758652017	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535656	CTCTCCTCCGAGGCA[C/T]AATCGCATCTGCCAC	3993
rs758667447	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75563972	ACGCTATTCACGTCT[C/T]TCAGCGGCCCAATTC	3993
rs758711674	snp	A/G	1.69026e-05	0.00290706	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571749	TGTGCCTCCCGCCGA[A/G]CGGAGAATGGATGAG	3993
rs758746471	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535660	CCTCCGAGGCACAAT[C/T]GCATCTGCCACTTAG	3993
rs758754250	snp	C/T	1.65682e-05	0.00287817	intron-variant	LLGL2	GRCh38.p7	17:75563836	TGGTCCTCTTTCCTC[C/T]CCAGAGCCTTCCTGG	3993
rs758762821	snp	A/G	1.69827e-05	0.00291394	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571693	TGCCCCTCGCTGTGG[A/G]CTGGCACCAATGGGG	3993
rs758913200	snp	A/G	0.000272294	0.011665	splice-acceptor-variant, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574212	GGCCTCTACCTTCCA[A/G]AGAAGCAGCCCGGCC	3993
rs758929778	snp	A/G	1.76015e-05	0.00296655	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570958	CTTGCAGGCACAGGA[A/G]GGGAGTGCCAAGGCT	3993
rs758942629	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75534511	TTTGAGAAAAGGTCT[C/T]GCTCTGTCACCCAGG	3993
rs758953390	snp	C/T	1.67239e-05	0.00289166	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559368	TGCCAGCTTTTCGTG[C/T]GCTGGAGGACCGGAC	3993
rs758955076	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566312	CCTCTGCTCCAGAAG[G/T]ATCTGTCTGGCTGCC	3993
rs759024622	snp	A/G	1.68136e-05	0.0028994	intron-variant	LLGL2	GRCh38.p7	17:75558272	CAGGAAGCCACTTCC[A/G]TGCCCTCCTTGCCTT	3993
rs759059197	snp	C/T	3.37998e-05	0.00411081	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573106	CAGCGTGGCCCACTT[C/T]GGCAGTCGTCGAGCC	3993
rs759070999	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545835	AGCCCAGCCAGTGGG[A/G]ATGGGAACGAGGCAT	3993
rs759089001	snp	C/T	1.66214e-05	0.00288278	intron-variant	LLGL2	GRCh38.p7	17:75569217	GGCCCCTCCCCTTCT[C/T]CAGGTGGGCTCCTTT	3993
rs759120013	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75540346	TCAAGGAAGCGTGGT[A/G]CTTTTCCATGCCTTG	3993
rs759127325	snp	A/G	1.70122e-05	0.00291647	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563350	TGGAGAACATCTGGT[A/G]GCAGCGGGACGGCCG	3993
rs759154613	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75562696	GCCTCCGCCTCCCAA[A/G]TAGCTGGGGTTATAG	3993
rs759216723	snp	A/G	1.65592e-05	0.00287738	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524456	GCTCCGGGGGACCGG[A/G]ACTGTCTGTTCTCAG	3993
rs759244006	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572333	ATCAGCCTGGCCAAT[A/G]TGGTGAAACCCTGAC	3993
rs759293550	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75527576	AGTAACTTTTTTCTC[-/T]TTTTTTTTTCTTTTT	3993
rs759310196	snp	C/T	1.7051e-05	0.0029198	intron-variant	LLGL2	GRCh38.p7	17:75571796	AGGGTGAGTGCTGGG[C/T]AGGGAGAGCAGAGGG	3993
rs759341750	snp	G/T	3.37069e-05	0.00410516	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570164	GTGGTCACCTCCTTG[G/T]CCCTGCACTCTGAGT	3993
rs759367196	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75544416	GTGAGACCAGACAGT[C/T]TGGAAAAGGGATGTC	3993
rs759389337	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75533598	CATGAGCCACCGCGC[C/G]CAGCCCGTTCAAGTA	3993
rs759393752	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75561741	GCTTGGGCAACATGG[C/T]GAAACCCCGTCTCTA	3993
rs759416803	snp	C/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523246	ATGTGACTCCCCTCC[C/T]CAGTACCTTGTTTTC	3993
rs759432308	snp	A/C/G	3.40897e-05	0.00412843	intron-variant	LLGL2	GRCh38.p7	17:75556017	AGGGGACAGGTCTGC[A/C/G]GGCCCACCCCACGTG	3993
rs759436881	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75543808	ATAAAACGATCTGCC[A/C]TGTCTACCTCGGCAC	3993
rs759466660	snp	A/G	2.23077e-05	0.00333967	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570086	CTGGCAGCCCGCTCA[A/G]GGCCCGTGCGCTTTG	3993
rs759539268	snp	C/T	1.76593e-05	0.00297142	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574652	CGCCGTGGGGTGCAG[C/T]CTCAGCAATGGCGGA	3993
rs759542664	snp	A/G	3.34431e-05	0.00408906	intron-variant	LLGL2	GRCh38.p7	17:75568708	GGTAGGTCTGGCCCT[A/G]GCCCCAGCCCCAGCC	3993
rs759549730	snp	A/G	3.74904e-05	0.00432941	intron-variant	LLGL2	GRCh38.p7	17:75568952	TGGCATCCCTCTCAC[A/G]CCTGGCAGGTGGGTT	3993
rs759590368	snp	C/T	3.02156e-05	0.00388676	intron-variant	LLGL2	GRCh38.p7	17:75557997	GGGCTGCTGTGTCTC[C/T]TCCCCACCCTAGGCT	3993
rs759597688	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555846	AGGGGTGGCCATGAG[A/G]CCAAGGGCAGAGTCA	3993
rs759611600	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75565464	CTTTTCTTTCTTTCT[C/T]AGCCTCTCCTCCCTC	3993
rs759655042	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536334	GTGTGTCACTTAAGT[A/G]CACAGCACCTGAGAG	3993
rs759670596	snp	A/G	2.18548e-05	0.00330559	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570385	CAGCTGGCCTTGGAG[A/G]GCCCACTCTCCCGCG	3993
rs759701548	snp	C/G	1.64746e-05	0.00287002	upstream-variant-2KB, missense, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524327	AGAGTGGGGATGTCC[C/G]TCTGATCTTTGCCCT	3993
rs759743512	in-del	-/CCAGAGCTTTCCTGAG	6.61266e-05	0.00574969	intron-variant	LLGL2	GRCh38.p7	17:75558127	ATGGTGTCCGACCTT[-/CCAGAGCTTTCCTGAG]CCAGAGCTTTCCTGA	3993
rs759765759	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558721	TTGTGAGGCCTGTTG[C/T]GCCCCTGGCAGTGAC	3993
rs759769413	snp	C/T	5.99287e-05	0.00547364	intron-variant	LLGL2	GRCh38.p7	17:75573659	GCCAGAGGCCTCTCC[C/T]GCCCCTCCCGCCCCT	3993
rs759796942	in-del	-/G	0.000230502	0.010733	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570209	TTCGGCACCAGCCAT[-/G]GCTTTGGCCTCTTTG	3993
rs759824476	snp	C/T	1.8335e-05	0.00302773	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523785	GCATTAGTGGGTACG[C/T]AGTGAGCCAGCACTG	3993
rs759825795	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531348	GGAGTTTAGTTTCCC[C/T]GGGGAGCTATTCGGC	3993
rs759853911	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545902	ATGATATTTGAGGCT[A/G]GCTGTGCTGCGGAGG	3993
rs759895942	snp	C/T	1.719e-05	0.00293167	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571916	AGGAGATCCAGCTGA[C/T]GCACCGGGCGCCGGT	3993
rs759921740	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75558101	GGGCCTGGCACTCAA[A/G]GCAGGCAGGGGATGG	3993
rs759922866	snp	A/G	0.000143748	0.00847663	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564571	GGGGCAGGACCATCA[A/G]TAAAGACAGGGCCAG	3993
rs759929022	snp	C/G	1.73576e-05	0.00294593	splice-donor-variant	LLGL2	GRCh38.p7	17:75559411	CGCGGTGCTGCAGCG[C/G]TGAGCCCAGAGCCCA	3993
rs759931517	snp	A/G	3.39236e-05	0.00411833	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571963	CTCGACGGACACAGC[A/G]TACCCCTTCCCGAGC	3993
rs759948976	snp	C/T	8.74898e-05	0.00661342	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573601	GCCCTGGTAACGGTG[C/T]GGGCCCCAAGAAGGC	3993
rs760016458	snp	C/T	1.6701e-05	0.00288968	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569298	CAAGTACAGCGGCTA[C/T]CTGGCTGTGGCAGGC	3993
rs760047758	snp	C/G	6.82967e-05	0.00584326	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564501	ACAGAGGCAGACCCT[C/G]CAGCCAGTAGGAGAG	3993
rs760070109	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75528892	GGCCGGGCAAGGTGG[C/G]TTATGCCTGTAATCC	3993
rs760074790	snp	A/G	8.22639e-05	0.00641289	intron-variant	LLGL2	GRCh38.p7	17:75558639	CAGGGTAAGGGCTCA[A/G]TCCCCAGCCCCTTCC	3993
rs760108198	snp	A/G	1.70449e-05	0.00291928	intron-variant	LLGL2	GRCh38.p7	17:75569332	GCAGGGCAGGTAGCA[A/G]GCTGGGCTGGGGAGG	3993
rs760153694	snp	A/G	1.72329e-05	0.00293533	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563022	CTCGCCCAGGTTGCC[A/G]GAGGAGGCCCGCCAC	3993
rs760202277	snp	C/T	1.69864e-05	0.00291426	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543386	CCCTGCAGCTCCTTC[C/T]GTTTCTCCAGGTCTC	3993
rs760232673	snp	C/T	3.34784e-05	0.00409122	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571053	CAGAGGACTCCTTCA[C/T]AGGCTTCGTCCGGAC	3993
rs760272763	snp	A/G	1.67002e-05	0.00288961	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543497	ACCTGTTCCAGTTTA[A/G]CAAGGTAAGTTAGGG	3993
rs760292447	snp	C/T	0.000114433	0.00756331	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558567	TTTGGAGCCTGAAGG[C/T]CAAGGGCGGGGCATC	3993
rs760339057	snp	C/T	5.67392e-05	0.00532601	intron-variant	LLGL2	GRCh38.p7	17:75569958	CCACCTGCCACCCTG[C/T]GCAGGTGCTGGTACT	3993
rs760383560	snp	A/C	1.6476e-05	0.00287014	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523373	CTCTGCAGTACCTTG[A/C]CCGCCAGGAGTTGGT	3993
rs760389496	snp	C/T	1.99635e-05	0.00315933	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574589	CCTGAGGCCATGACT[C/T]CCCTGTCTTTGCCTG	3993
rs760397179	snp	C/T	0.00307316	0.0390786	intron-variant	LLGL2	GRCh38.p7	17:75573665	GGCCTCTCCCGCCCC[C/T]CCCGCCCCTCCCTGC	3993
rs760411684	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523850	CCAAGTGGGACTCCT[C/T]TGTACTCCCCTGGCC	3993
rs760449037	snp	A/G	5.50812e-05	0.00524763	intron-variant	LLGL2	GRCh38.p7	17:75570268	TAAGTGAGCAGGGGC[A/G]GCTGGGTCCCGGGGC	3993
rs760452145	snp	C/T	9.05772e-05	0.00672907	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573608	TAACGGTGCGGGCCC[C/T]AAGAAGGCCCCGAGC	3993
rs760469962	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75543753	CTCTGCAAGTCACTC[C/T]ACCTCATGGAGCCTC	3993
rs760487213	snp	C/G	1.79396e-05	0.00299491	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568819	CCCAGCCCCACCCCA[C/G]AGGGACCTGCTGCTC	3993
rs760536508	in-del	-/GGGGA	5.55098e-05	0.005268	intron-variant	LLGL2	GRCh38.p7	17:75570902	CGAAGCACTGTTCCT[-/GGGGA]GGGGAGTCCAGAGCT	3993
rs760573259	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75553247	GGCCCTATCTGTCCC[C/G]CTGGCTATCCCATTT	3993
rs760625625	snp	G/T	1.68238e-05	0.00290028	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573175	CCTGGGCGACATCCA[G/T]GTGGTCTCGCTGCCC	3993
rs760648749	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75526418	GGAGACCCAGTCTGC[C/T]CTCCATGCTGACGGG	3993
rs760690036	snp	A/G	4.96052e-05	0.00497998	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563799	CTCTGGCTGACCACT[A/G]GGCAGGGGTAGGTAT	3993
rs760703932	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75565766	GGGTGCCTGATGAGC[A/G]GTGCTTCCCTCAGAT	3993
rs760735734	snp	C/G	1.76789e-05	0.00297307	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569054	AAACTCAGCACTGTG[C/G]GCGTGTTCCTCACCG	3993
rs760743054	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75574030	GCCACACCCGGCCCA[C/G]ACCTGGGGCTGGACG	3993
rs760793840	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75553318	GCCAGGCCTGAGGCA[-/C]CCCCCCGTCTCCCCC	3993
rs760842535	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535245	AACAGGAGGCCACAG[C/T]CACACTCAGGCCTCA	3993
rs760867818	in-del	-/GCCCTGG	0.000162933	0.0090244	intron-variant, splice-acceptor-variant	LLGL2	GRCh38.p7	17:75574110	ACGGCATTCCTTCCA[-/GCCCTGG]GCCCTGGGCTTCCAC	3993
rs760890911	snp	C/G	1.7528e-05	0.00296036	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559286	CAGATCACCGTGGTC[C/G]TGCCACATTCCTCCT	3993
rs760917491	snp	A/G	3.35739e-05	0.00409705	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564388	AGGGTGGCATGCCAC[A/G]GGCCAGCTACGGGGA	3993
rs760960405	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567057	CATGGGACAGCTGAG[C/T]CCGGGCACCCTCAAG	3993
rs760962713	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528702	AAGATCACGCCATTG[C/T]ACTCCAGCCTGAGCA	3993
rs761050076	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567762	GCCTGAGCAACATGG[C/T]GAAACCCTGTCTCTA	3993
rs761064960	snp	C/T	2.28836e-05	0.00338249	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570397	GAGGGCCCACTCTCC[C/T]GCGTCAAGTCCCTCA	3993
rs761067630	snp	A/G	7.36811e-05	0.00606919	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570459	GCGTCGGAGCCGGGT[A/G]TCCAGCCGGAAGCGG	3993
rs761073701	snp	C/T	1.65141e-05	0.00287346	intron-variant	LLGL2	GRCh38.p7	17:75574850	CAGGGTGATCTTGAG[C/T]TGTCCCTCTGTGTCC	3993
rs761084556	snp	C/T	1.84521e-05	0.00303738	intron-variant	LLGL2	GRCh38.p7	17:75572071	CAGTTCAAGGTGCCA[C/T]ACGGGCAGCGGCGGG	3993
rs761137686	snp	A/C/G	1.69766e-05	0.00291342	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571975	AGCGTACCCCTTCCC[A/C/G]AGCCCCTCGAAGTGG	3993
rs761140435	snp	C/T	1.67854e-05	0.00289697	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568530	AGGAGCTGGTGGTGA[C/T]TGACCTGCAGACAGC	3993
rs761148543	snp	C/T	1.80935e-05	0.00300773	intron-variant	LLGL2	GRCh38.p7	17:75568971	GGCAGGTGGGTTCTG[C/T]CCACAGGCACGAGGA	3993
rs761184078	snp	A/C	0.000102265	0.00714997	intron-variant	LLGL2	GRCh38.p7	17:75574022	ACACCTGGGCCACAC[A/C]CGGCCCAGACCTGGG	3993
rs761207046	snp	C/T	1.89285e-05	0.00307634	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523798	CGCAGTGAGCCAGCA[C/T]TGCCCCTCCCCCAGC	3993
rs761207269	snp	C/T	1.65135e-05	0.00287341	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558163	CTCCTAGCTACGGAG[C/T]CCCAGGCGTGGAGTT	3993
rs761228976	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75531127	CTGTGCTGCTCTGTT[A/G]GCATTAGGAGACTTT	3993
rs761250734	snp	A/G	3.35334e-05	0.00409458	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568544	ATTGACCTGCAGACA[A/G]CAGGCTGGCCACCGG	3993
rs761297221	snp	A/G	1.66032e-05	0.0028812	intron-variant	LLGL2	GRCh38.p7	17:75558099	GAGGGCCTGGCACTC[A/G]AGGCAGGCAGGGGAT	3993
rs761350344	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75570796	TCCCCCAAGGGCACC[C/T]CCCTCTTGGACAAGG	3993
rs761372858	snp	C/G	3.43631e-05	0.00414492	intron-variant	LLGL2	GRCh38.p7	17:75556003	CCATGGTGGCGCGAA[C/G]GGGACAGGTCTGCAG	3993
rs761379338	snp	A/G	3.68942e-05	0.00429485	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569975	CAGGTGCTGGTACTG[A/G]AACTGAATGACGAGG	3993
rs761400190	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75531831	TGGCTTTGAATACTC[A/T]CCCCTCTCTTCTTCC	3993
rs761441211	snp	C/G	1.64819e-05	0.00287066	intron-variant	LLGL2	GRCh38.p7	17:75543532	CAGGGAAGATGACCC[C/G]CAGGTTTTCGGCCAA	3993
rs761463266	snp	C/G	0.00010856	0.00736669	intron-variant	LLGL2	GRCh38.p7	17:75559239	GGCTCACGGGCAGCT[C/G]TTCTTGTCACAGGGC	3993
rs761472288	snp	C/T	3.35014e-05	0.00409262	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571064	TTCACAGGCTTCGTC[C/T]GGACCCTGTACTTTG	3993
rs761474129	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75547445	CTCTCTGTTCTTTAG[G/T]TTCCTCATCTGTAAA	3993
rs761481757	snp	A/G	4.98857e-05	0.00499403	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568630	CGTCTCCAACATCCC[A/G]CTGAAGCTGTGGGAG	3993
rs761496736	snp	A/G	1.71908e-05	0.00293174	intron-variant	LLGL2	GRCh38.p7	17:75563509	CCCCCAGTGCCTCCT[A/G]GATTCAGGTGCAGGT	3993
rs761502190	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542949	CCTCTCCCCTGCCCC[A/G]ACTTGGGCTCTGATC	3993
rs761529667	snp	A/G	3.36848e-05	0.00410381	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573197	TCGCTGCCCCTGCTC[A/G]AGCCCCAGGTGCGCT	3993
rs761538819	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75552065	ACCCGGGAGGTGGAG[G/T]TTGCAGCGAGCTAAG	3993
rs761550152	snp	C/T	1.90271e-05	0.00308435	intron-variant	LLGL2	GRCh38.p7	17:75568944	ATCCCGGCTGGCATC[C/T]CTCTCACGCCTGGCA	3993
rs761596245	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562732	TGCCACCACGCCCAG[C/T]TAATGTTTTATATTT	3993
rs761663454	in-del	-/CCT	1.76543e-05	0.002971	intron-variant	LLGL2	GRCh38.p7	17:75571884	CAGCCCCAACACCCA[-/CCT]CCTCCCCCTAGCCAA	3993
rs761712480	snp	A/G	1.70749e-05	0.00292184	intron-variant	LLGL2	GRCh38.p7	17:75569342	TAGCAGGCTGGGCTG[A/G]GGAGGGGGAGCTGGG	3993
rs761720572	in-del	-/A	3.53551e-05	0.00420432	frameshift-variant, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574656	GTGGGGTGCAGCCTC[-/A]GCAATGGCGGAGGTG	3993
rs761736519	snp	C/T	1.68829e-05	0.00290537	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563445	CAACCAGAGCCCCTC[C/T]GCAGCCTCGTGCCTT	3993
rs761786563	snp	C/G	1.73084e-05	0.00294175	intron-variant	LLGL2	GRCh38.p7	17:75571625	CAGCTCCACCCGACT[C/G]CCACGCTAAGGGTCA	3993
rs761815831	snp	C/T	3.38169e-05	0.00411185	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571746	GCGTGTGCCTCCCGC[C/T]GAGCGGAGAATGGAT	3993
rs761877490	snp	C/T	5.79123e-05	0.00538078	intron-variant	LLGL2	GRCh38.p7	17:75558653	AATCCCCAGCCCCTT[C/T]CACTCCCAGCCCAGC	3993
rs761898691	snp	A/G	5.08031e-05	0.00503974	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573503	CCTGATCTCACCCTC[A/G]GAGTTTGAGCGCTTC	3993
rs761934874	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537431	GGGTGCGGTGGCTCA[C/T]GCCTATAATCCTAGC	3993
rs761937745	snp	C/T	0.000427215	0.0146091	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564476	CCGTGTCATCGGCTT[C/T]ACTGTCCTCACAGAG	3993
rs761967911	snp	G/T	1.6612e-05	0.00288196	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556118	CGCATCCTGGCCATC[G/T]GCACCCGTTCTGGAG	3993
rs761988052	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544495	TTTGAGAACTGTAGA[A/G]GTCAGCTTGCCCAGG	3993
rs762056131	snp	A/G	0.000103061	0.00717773	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559399	CATCAGCTCGGACGC[A/G]GTGCTGCAGCGGTGA	3993
rs762057705	snp	C/T	5.00847e-05	0.00500398	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556078	CCCGCACCAGCCCAG[C/T]GCCCTCGGCTACAGC	3993
rs762070531	snp	C/T	0.000116439	0.00762929	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570182	CTGCACTCTGAGTGG[C/T]GGCTCGTGGCCTTCG	3993
rs762071337	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549658	CGGGCAGAGTGGCCC[A/G]GCCAGGCAGGAGTGC	3993
rs762084243	snp	A/C			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567677	CTGGGCACAGTGGCT[A/C]ATGCCTGTAATCCCA	3993
rs762114963	in-del	-/AAA			intron-variant	LLGL2	GRCh38.p7	17:75569802	AGCAAGACTTGTCTC[-/AAA]AAAAAAAAAAAAAAA	3993
rs762137533	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566840	CTCTGATCTCCAGAC[C/G]CATAAGGGAGATGCT	3993
rs762170189	snp	A/G	1.7626e-05	0.00296861	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569057	CTCAGCACTGTGCGC[A/G]TGTTCCTCACCGACA	3993
rs762180678	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524454	TTGCTCCGGGGGACC[A/G]GGACTGTCTGTTCTC	3993
rs762259166	in-del	-/AAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75550783	GAGACCCTGTCTCAA[-/AAAAAA]AAAAAAAAAAAAAAA	3993
rs762283011	snp	A/G	1.68798e-05	0.0029051	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563178	CTTCCTCAGCAGCCA[A/G]GTAGGCAGTGCCCAG	3993
rs762299544	snp	C/G	1.73114e-05	0.002942	intron-variant	LLGL2	GRCh38.p7	17:75573433	CAGGTGGGGAGGCAG[C/G]CTTGGCAGCCGCCAG	3993
rs762306081	snp	A/C			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568327	CACACCTGCTGCCCT[A/C]CTGGAGATGGAAAGG	3993
rs762316279	snp	C/T	4.99938e-05	0.00499944	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568692	CACACTTCTCCACCA[C/T]GGTAGGTCTGGCCCT	3993
rs762321284	snp	C/T	0.000159515	0.00892928	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570466	AGCCGGGTGTCCAGC[C/T]GGAAGCGGCACCCGG	3993
rs762328870	snp	A/G	1.77347e-05	0.00297776	intron-variant	LLGL2	GRCh38.p7	17:75573006	GAACAACCACCCCAC[A/G]CCCCCAGGTGTTCAC	3993
rs762349847	snp	C/T	1.6489e-05	0.00287128	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524424	CTGACCTCACAGCTC[C/T]GCAGAGGATGGAGCT	3993
rs762395658	snp	A/G	1.69654e-05	0.00291246	intron-variant	LLGL2	GRCh38.p7	17:75563192	AGGTAGGCAGTGCCC[A/G]GGACATGGCAGGCGC	3993
rs762414335	snp	C/T			upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524274	CAGATTTGATGAGCC[C/T]GTCCCAGACCTCTGC	3993
rs762435393	snp	C/G	1.64746e-05	0.00287002	upstream-variant-2KB, missense, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524313	GCGGTTGTCTTACCA[C/G]AGTGGGGATGTCCCT	3993
rs762463307	snp	A/G	0.000112899	0.00751243	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574405	GGAAGGGCTGTGGCT[A/G]GCCGCCCCAAGGGCC	3993
rs762490027	snp	A/G	0.0004566	0.0151027	intron-variant, splice-donor-variant	LLGL2	GRCh38.p7	17:75570511	GAGGTGAGGCCTGAG[A/G]TGAGGCTGCGGCCGG	3993
rs762514835	in-del	-/TG	0.000132092	0.00812579	intron-variant	LLGL2	GRCh38.p7	17:75574859	CTTGAGCTGTCCCTC[-/TG]TGTCCTTCAGCAGAG	3993
rs762536293	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542797	CTGACCGAGTGCTCT[A/G]TGCCACCCGTGCCCA	3993
rs762536309	snp	C/T	3.84084e-05	0.00438209	intron-variant	LLGL2	GRCh38.p7	17:75572083	CCACACGGGCAGCGG[C/T]GGGTCTCCCTGGGAC	3993
rs762545357	in-del	-/CAAA			intron-variant	LLGL2	GRCh38.p7	17:75527167	AGTGAGACCCTGTCT[-/CAAA]AAAAAAAAAAAAAAG	3993
rs762561612	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75551934	AGGAGTTCGAGACCA[G/T]CCTGGCCAACATGGT	3993
rs762593534	snp	G/T	1.66266e-05	0.00288323	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568641	TCCCGCTGAAGCTGT[G/T]GGAGCGGATCATTGC	3993
rs762688905	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75550205	GCTATGCCCCGTCCC[A/G]CCCTCTGTCCTGAGT	3993
rs762853275	snp	C/T	1.86156e-05	0.00305081	intron-variant	LLGL2	GRCh38.p7	17:75573311	GGTGGGTGTCGGGGC[C/T]CCGGGCACTGCACGG	3993
rs762870079	snp	C/G	5.90545e-05	0.00543358	intron-variant	LLGL2	GRCh38.p7	17:75558656	CCCCAGCCCCTTCCA[C/G]TCCCAGCCCAGCCTG	3993
rs762899289	snp	C/T	3.43666e-05	0.00414513	intron-variant	LLGL2	GRCh38.p7	17:75571646	CTAAGGGTCAGACAC[C/T]CAAACATGGCTTCTC	3993
rs762917323	snp	C/T	1.66092e-05	0.00288172	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556124	CTGGCCATCGGCACC[C/T]GTTCTGGAGCCATCA	3993
rs762924049	snp	C/T	3.3442e-05	0.004089	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556063	GGTGGAGCATGGCTT[C/T]CCGCACCAGCCCAGC	3993
rs762927212	snp	C/T	1.94399e-05	0.00311763	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570068	TGGAAGGGGCACGAG[C/T]GCCTGGCAGCCCGCT	3993
rs763070886	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566057	TCCCTGATAAGGGGA[C/T]GTATTTGCGCAGACA	3993
rs763077725	snp	C/T	1.75745e-05	0.00296428	intron-variant	LLGL2	GRCh38.p7	17:75571887	CCCCAACACCCACCT[C/T]CTCCCCCTAGCCAAG	3993
rs763099057	snp	C/T	0.000132133	0.00812706	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523714	TGATGTTTACCAGGC[C/T]GACGCTGTGGCCACA	3993
rs763113069	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75537591	TAATTCCAGCTACTT[C/G]GGAGGCTGAGGCAGG	3993
rs763192710	snp	G/T	1.64768e-05	0.00287021	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523384	CTTGACCGCCAGGAG[G/T]TGGTGGTTAGGAACT	3993
rs763215837	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75559698	GTCCTTTGCACTTGC[C/T]ATGGGTTTCAGAACC	3993
rs763251593	snp	A/C			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542277	GCCTCCCACTTCGGG[A/C]CAGGTGTTCCCTCTC	3993
rs763257356	snp	C/T	1.69292e-05	0.00290935	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573513	CCCTCGGAGTTTGAG[C/T]GCTTCTCTCTCTCCA	3993
rs763267912	snp	A/G	1.76758e-05	0.00297281	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574648	GAGCCGCCGTGGGGT[A/G]CAGCCTCAGCAATGG	3993
rs763298452	in-del	-/C	1.70051e-05	0.00291586	intron-variant	LLGL2	GRCh38.p7	17:75543528	GAGCAGGGAAGATGA[-/C]CCCCCAGGTTTTCGG	3993
rs763301170	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75527166	AGTGAGACCCTGTCT[-/AA]CAAAAAAAAAAAAAA	3993
rs763337867	snp	A/G			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565040	CCTCCTGTCTGCCCC[A/G]GGCTCTCTGCCCTTT	3993
rs763348168	snp	A/C	3.33489e-05	0.0040833	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564407	CAGCTACGGGGACCG[A/C]CACTGCATCTCAGTG	3993
rs763363079	snp	A/T	3.34851e-05	0.00409163	intron-variant	LLGL2	GRCh38.p7	17:75558262	TGGGGTGGGACAGGA[A/T]GCCACTTCCATGCCC	3993
rs763417692	snp	A/G	1.72207e-05	0.00293429	intron-variant	LLGL2	GRCh38.p7	17:75571817	GAGCAGAGGGTGCTC[A/G]GGCTGCCTGGGCTGG	3993
rs763434855	snp	C/T	1.80299e-05	0.00300243	intron-variant	LLGL2	GRCh38.p7	17:75570941	CTTAGGCTGGCCCAC[C/T]CCTTGCAGGCACAGG	3993
rs763475439	snp	C/T	0.000152878	0.0087416	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569126	GAGTGGCCCCCACTC[C/T]GCAAGGTGAGGCCAG	3993
rs763494457	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75537505	TCGAGACCAGCCTGG[A/C]CAATATGGTGAAAAC	3993
rs763545776	snp	A/G	1.68729e-05	0.00290451	missense, intron-variant	LLGL2	GRCh38.p7	17:75564525	AGGAGAGCTTCGGGA[A/G]TGGGTGCCCAGGGTT	3993
rs763564571	snp	A/C	9.95305e-05	0.00705375	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569246	TTGACCCCTACAGTG[A/C]TGACCCCCGGCTGGG	3993
rs763566228	snp	A/G	1.69533e-05	0.00291142	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543397	CTTCTGTTTCTCCAG[A/G]TCTCCAGTGGGGGCT	3993
rs763580966	snp	A/G	1.68972e-05	0.0029066	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564491	CACTGTCCTCACAGA[A/G]GCAGACCCTGCAGCC	3993
rs763595192	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75556273	CCTGATTTCCAGTTT[G/T]GGACATGATTTTATT	3993
rs763621790	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75569337	GCAGGTAGCAGGCTG[A/G]GCTGGGGAGGGGGAG	3993
rs763622711	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75541095	GTGCTCAGTGTCCAC[A/G]CCCTCCTGATGCCAT	3993
rs763623087	snp	C/G	3.34874e-05	0.00409177	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543501	GTTCCAGTTTAACAA[C/G]GTAAGTTAGGGAGAG	3993
rs763663044	snp	A/G	0.000145241	0.00852052	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573613	GTGCGGGCCCCAAGA[A/G]GGCCCCGAGCCGAGC	3993
rs763705160	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75551936	GAGTTCGAGACCAGC[C/G]TGGCCAACATGGTGA	3993
rs763712906	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75557334	CCCACAGGCGGCAGA[C/G]AGTGGAGAGGGCTCT	3993
rs763732778	snp	A/G			intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523567	GTGGCACCTCTGTGA[A/G]GCTGCTTCCTGGAAC	3993
rs763747053	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75550962	CCTGTTCCCAAATCC[C/G]AATCCCTTCCCTGTT	3993
rs763777264	snp	C/T	1.69761e-05	0.00291337	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571978	GTACCCCTTCCCGAG[C/T]CCCTCGAAGTGGCCC	3993
rs763829419	in-del	-/CTTGCCCC	1.6838e-05	0.0029015	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563168	GCTCTACCACTTCCT[-/CTTGCCCC]CAGCAGCCAGGTAGG	3993
rs763842811	snp	A/G			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568330	ACCTGCTGCCCTCCT[A/G]GAGATGGAAAGGCTT	3993
rs763855012	snp	C/T	2.00753e-05	0.00316816	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568440	CTGGGCTGCTTCCTC[C/T]TGGCCCCGGCCCCTG	3993
rs763892627	snp	C/T	7.99307e-05	0.00632131	intron-variant	LLGL2	GRCh38.p7	17:75573668	CTCTCCCGCCCCTCC[C/T]GCCCCTCCCTGCCCT	3993
rs763904224	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75565861	CCTTGGTAGGCTCTC[C/G]TGTTTAATGAGCAAC	3993
rs763918138	snp	C/T	1.64765e-05	0.00287019	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523374	TCTGCAGTACCTTGA[C/T]CGCCAGGAGTTGGTG	3993
rs763936036	snp	C/T	4.56017e-05	0.00477481	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558574	CCTGAAGGTCAAGGG[C/T]GGGGCATCGGAGCTG	3993
rs763958592	snp	A/C/T	3.34913e-05	0.00409201	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571060	CTCCTTCACAGGCTT[A/C/T]GTCCGGACCCTGTAC	3993
rs763964803	snp	A/G	1.65982e-05	0.00288077	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569233	CAGGTGGGCTCCTTT[A/G]ACCCCTACAGTGATG	3993
rs763984358	snp	A/G	0.000102022	0.00714146	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563361	TGGTGGCAGCGGGAC[A/G]GCCGCCTGCTCGTCA	3993
rs764009284	snp	C/T	3.36814e-05	0.0041036	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573183	ACATCCAGGTGGTCT[C/T]GCTGCCCCTGCTCAA	3993
rs764012469	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75545946	TGTAGATTATTTAGC[A/T]GTGTCCCTAGTCCTA	3993
rs764024504	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562768	AGAGACAGGGTTTTG[C/T]CATGTTGGCCAGGCT	3993
rs764035220	in-del	-/G	1.76142e-05	0.00296762	intron-variant	LLGL2	GRCh38.p7	17:75571121	GGCCAGCCTGGGGTT[-/G]GGGGGGCAGGGGGTA	3993
rs764054651	snp	C/T	0.000150218	0.00866524	intron-variant	LLGL2	GRCh38.p7	17:75573328	CGGGCACTGCACGGA[C/T]GGGAAGGGTGGCCAG	3993
rs764062126	snp	A/C			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526039	ACTTCTCTGCCTGAT[A/C]TGCGCGATGACTGAA	3993
rs764094652	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75534033	GGGCAGGTAGGAGGC[C/T]CTAGAAAGGGGCCTG	3993
rs764103738	snp	A/G	1.74202e-05	0.00295124	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559288	GATCACCGTGGTCCT[A/G]CCACATTCCTCCTGC	3993
rs764134542	in-del	-/AGT			intron-variant	LLGL2	GRCh38.p7	17:75535196	CACCAGTGCCATCAG[-/AGT]AGGAGGTGCAGGGGC	3993
rs764163617	snp	A/G	1.65375e-05	0.0028755	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563803	GGCTGACCACTAGGC[A/G]GGGGTAGGTATCCAT	3993
rs764223531	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75554212	GAGACTGAGGCAGGA[A/G]AATCACTTGAACCTG	3993
rs764235741	in-del	-/AGGCATCCCCCAAAAT			intron-variant	LLGL2	GRCh38.p7	17:75553349	GACCTTTTTGTCTCC[-/AGGCATCCCCCAAAAT]AGGCACTTGTTGGAG	3993
rs764251588	snp	A/C	0.000144833	0.00850856	intron-variant, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574158	AGTAAGGAGAGAGAG[A/C]GCCAGGCCGAGGAGG	3993
rs764287689	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75526718	TTTGTAGTTCAAGAG[A/C]ACCTTGAGTTCTCTT	3993
rs764292060	snp	A/G/T	5.07175e-05	0.00503553	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571744	CTGCGTGTGCCTCCC[A/G/T]CCGAGCGGAGAATGG	3993
rs764296862	snp	A/G	1.66738e-05	0.00288732	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559337	ACCGAGAGTGGCAAC[A/G]TGTTTGTGGTGCAGC	3993
rs764377907	snp	A/C	1.67781e-05	0.00289634	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563108	AGATCCTGATCGGCT[A/C]CAGCCGAGGCCTCGT	3993
rs764390322	snp	A/G	4.57383e-05	0.00478195	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570398	AGGGCCCACTCTCCC[A/G]CGTCAAGTCCCTCAA	3993
rs764401069	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536395	AAAGCCTCGGGACGA[C/T]GGAATAGAAAAGTCC	3993
rs764419820	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566070	GACGTATTTGCGCAG[A/T]CACGGAAGCAGTCTG	3993
rs764540023	snp	C/T	1.65919e-05	0.00288022	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574951	GGTCCCTGCCCCAAC[C/T]GGAGAGGCCGGTGCA	3993
rs764549732	snp	C/T	1.8011e-05	0.00300087	intron-variant	LLGL2	GRCh38.p7	17:75568973	CAGGTGGGTTCTGCC[C/T]ACAGGCACGAGGACG	3993
rs764575191	snp	A/G	2.27059e-05	0.00336933	intron-variant	LLGL2	GRCh38.p7	17:75558015	CCCACCCTAGGCTCC[A/G]TGCATGGGTCCTGCT	3993
rs764597230	snp	C/T	1.65141e-05	0.00287346	intron-variant	LLGL2	GRCh38.p7	17:75574851	AGGGTGATCTTGAGC[C/T]GTCCCTCTGTGTCCT	3993
rs764620516	snp	C/T	5.28304e-05	0.0051393	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573262	CGCCTCCTGCGTCTT[C/T]ACCAAATATGGCCAA	3993
rs764647144	snp	A/G	0.000105837	0.00727374	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569055	AACTCAGCACTGTGC[A/G]CGTGTTCCTCACCGA	3993
rs764685363	snp	C/G	5.75005e-05	0.00536162	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523802	GTGAGCCAGCACTGC[C/G]CCTCCCCCAGCTGCT	3993
rs764699136	snp	C/G	1.67624e-05	0.00289498	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570462	TCGGAGCCGGGTGTC[C/G]AGCCGGAAGCGGCAC	3993
rs764785017	snp	C/T	0.00010214	0.00714559	intron-variant	LLGL2	GRCh38.p7	17:75574023	CACCTGGGCCACACC[C/T]GGCCCAGACCTGGGG	3993
rs764788343	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549972	CTTTCCCAACCCCCC[C/T]GTCAAAAGAGTTCAT	3993
rs764791461	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75539432	TTTTTTTAGAGACAG[A/G]GTCTCACTATGTTGC	3993
rs764795955	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75540460	GAGGTCCCAGCCCCG[A/T]GTGGGAAGAGCAGCA	3993
rs764814251	snp	A/G	3.40177e-05	0.00412404	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571990	GAGCCCCTCGAAGTG[A/G]CCCATGATCTGTCGA	3993
rs764834292	snp	A/G	6.75379e-05	0.00581071	intron-variant	LLGL2	GRCh38.p7	17:75563181	CCTCAGCAGCCAGGT[A/G]GGCAGTGCCCAGGAC	3993
rs764839579	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567220	TGTAATCCTAGCACT[C/T]TGGGAGGCCAAGGAT	3993
rs764867842	snp	C/T			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565119	GATTTAACACCCACC[C/T]CGCTGAGGCAAGAGG	3993
rs764873932	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75533642	CTTGTGTGGTTCTAG[A/G]TGTTGGATGTGATCC	3993
rs764883995	snp	C/G	1.71649e-05	0.00292953	intron-variant	LLGL2	GRCh38.p7	17:75556005	ATGGTGGCGCGAAGG[C/G]GACAGGTCTGCAGGC	3993
rs764920758	snp	A/G	1.68088e-05	0.00289899	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570467	GCCGGGTGTCCAGCC[A/G]GAAGCGGCACCCGGC	3993
rs764942221	snp	C/G	6.6235e-05	0.0057544	intron-variant	LLGL2	GRCh38.p7	17:75558111	CTCAAGGCAGGCAGG[C/G]GATGGTGTCCGACCT	3993
rs765041772	in-del	-/G	8.9048e-05	0.00667204	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574671	AGCAATGGCGGAGGT[-/G]GGGGCTCTGGGCTTG	3993
rs765047154	snp	G/T	2.52165e-05	0.00355072	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570418	AAGTCCCTCAAGAAG[G/T]CCTTGCGTCAGTCAT	3993
rs765048911	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75547539	ATGAATTAAATTGAC[A/G]AGAGGCGGGGCGCAG	3993
rs765050159	snp	C/T	0.00013278	0.00814693	intron-variant	LLGL2	GRCh38.p7	17:75573671	TCCCGCCCCTCCCGC[C/T]CCTCCCTGCCCTCTC	3993
rs765061795	snp	C/T	5.7919e-05	0.00538109	intron-variant	LLGL2	GRCh38.p7	17:75558654	ATCCCCAGCCCCTTC[C/T]ACTCCCAGCCCAGCC	3993
rs765070983	snp	A/C	3.6787e-05	0.00428861	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569978	GTGCTGGTACTGGAA[A/C]TGAATGACGAGGCAG	3993
rs765089466	snp	C/T	1.65611e-05	0.00287755	intron-variant	LLGL2	GRCh38.p7	17:75563701	GCCTGTGGGGACTGA[C/T]ACTTGTCTGAGAGTT	3993
rs765125785	snp	C/T	1.72946e-05	0.00294058	intron-variant	LLGL2	GRCh38.p7	17:75571629	TCCACCCGACTCCCA[C/T]GCTAAGGGTCAGACA	3993
rs765144268	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544464	GAAGTCTCTTTGGTT[A/G]TATTTTTGTTATTGA	3993
rs765149693	snp	G/T	2.27368e-05	0.00337163	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558578	AAGGTCAAGGGCGGG[G/T]CATCGGAGCTGCAGG	3993
rs765162546	snp	C/T			upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524385	CAGCTTCAGGGACTT[C/T]ACGTTGCCCCAGGAT	3993
rs765167029	snp	G/T	3.44418e-05	0.00414966	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559402	CAGCTCGGACGCGGT[G/T]CTGCAGCGGTGAGCC	3993
rs765185968	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75543814	CGATCTGCCATGTCT[A/C]CCTCGGCACAGGGTT	3993
rs765192866	snp	C/T	6.78587e-05	0.0058245	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571962	GCTCGACGGACACAG[C/T]GTACCCCTTCCCGAG	3993
rs765238069	snp	A/G/T	6.67817e-05	0.00577815	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556079	CCGCACCAGCCCAGC[A/G/T]CCCTCGGCTACAGCC	3993
rs765252496	snp	A/G	1.71076e-05	0.00292464	intron-variant	LLGL2	GRCh38.p7	17:75571810	GCAGGGAGAGCAGAG[A/G]GTGCTCGGGCTGCCT	3993
rs765259472	snp	A/G/T	8.55287e-05	0.00653899	intron-variant	LLGL2	GRCh38.p7	17:75569346	AGGCTGGGCTGGGGA[A/G/T]GGGGAGCTGGGGAGG	3993
rs765285269	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75552394	CTCAGGAGGCTGAGG[C/T]GGGAGGATCACTTGA	3993
rs765378111	snp	A/G	2.3627e-05	0.00343699	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570094	CCGCTCAGGGCCCGT[A/G]CGCTTTGAGCCTGGC	3993
rs765379933	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75526472	GCGAGAAGTGGAAAA[C/T]TCTATCTTGCCAAAG	3993
rs765389510	snp	C/T	1.71085e-05	0.00292471	synonymous-codon, intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574490	CACACTGGAGGGAGA[C/T]CGCGGGTGAGGCACC	3993
rs765413326	snp	A/G	7.46241e-05	0.0061079	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570183	TGCACTCTGAGTGGC[A/G]GCTCGTGGCCTTCGG	3993
rs765424059	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567787	TCTCTACCAAAAATA[C/T]AAAAGTTAGCTGGGT	3993
rs765431729	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536345	AAGTGCACAGCACCT[A/G]AGAGTTTGCCAAGCC	3993
rs765433913	snp	A/G	1.64732e-05	0.0028699	missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523290	CCGTGGTCCTTCAGC[A/G]TATCTCTGTGCTGCA	3993
rs765450177	snp	C/T	1.64743e-05	0.00287	upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524316	GTTGTCTTACCAGAG[C/T]GGGGATGTCCCTCTG	3993
rs765453330	snp	C/G/T			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565039	ACCTCCTGTCTGCCC[C/G/T]GGGCTCTCTGCCCTT	3993
rs765457012	snp	C/T	1.98955e-05	0.00315395	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574590	CTGAGGCCATGACTC[C/T]CCTGTCTTTGCCTGT	3993
rs765539651	snp	A/G	3.30251e-05	0.00406343	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558171	TACGGAGCCCCAGGC[A/G]TGGAGTTCATGGGGC	3993
rs765542497	snp	C/G	1.68258e-05	0.00290045	intron-variant	LLGL2	GRCh38.p7	17:75568723	GGCCCCAGCCCCAGC[C/G]CCACCGCAAGCCAAA	3993
rs765585185	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75563920	CTCTCAGGTCCCGTG[A/T]TGGGGTCTTGGACAC	3993
rs765615830	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75553329	AGGCACCCCCCGTCT[-/C]CCCCGACCTTTTTGT	3993
rs765637540	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75550780	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs765646451	snp	A/G			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568069	AAAATGCCACCCCTA[A/G]CAACTGGTGTGCTGA	3993
rs765669715	snp	A/G	1.69292e-05	0.00290935	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573505	TGATCTCACCCTCGG[A/G]GTTTGAGCGCTTCTC	3993
rs765685177	snp	C/T	3.29745e-05	0.00406031	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523827	GCTGCTGCCAGTTCT[C/T]CTGTGAACCAAGTGG	3993
rs765704394	snp	C/T	6.82408e-05	0.00584087	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559301	CTGCCACATTCCTCC[C/T]GCGAGCTGCTCTACC	3993
rs765711964	snp	C/G	1.65452e-05	0.00287616	intron-variant	LLGL2	GRCh38.p7	17:75563819	GGGGTAGGTATCCAT[C/G]CTGGTCCTCTTTCCT	3993
rs765727454	snp	G/T	8.35038e-05	0.00646103	intron-variant, stop-gained	LLGL2	GRCh38.p7	17:75570508	GGAGAGGTGAGGCCT[G/T]AGGTGAGGCTGCGGC	3993
rs765727465	snp	C/T	3.51389e-05	0.00419144	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569067	TGCGCGTGTTCCTCA[C/T]CGACACGGACCCCAA	3993
rs765780331	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535483	GATCAATGGAACTTC[C/T]CGAGCTATGGAGGGA	3993
rs765796159	snp	A/C	3.45901e-05	0.00415859	intron-variant	LLGL2	GRCh38.p7	17:75573442	AGGCAGCCTTGGCAG[A/C]CGCCAGGCCAGGCCG	3993
rs765814725	snp	A/G	6.60917e-05	0.00574817	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558194	CATGGGGCTGCACCA[A/G]GAGAACAACGCTGTG	3993
rs765815544	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528954	ACAAGGTCAGGAGTT[C/T]GAGACTAGCCTTGCC	3993
rs765875965	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537450	TATAATCCTAGCACT[C/T]TGTGGGGCCGAGGTG	3993
rs765880962	snp	A/G	1.70119e-05	0.00291644	intron-variant	LLGL2	GRCh38.p7	17:75563203	GCCCAGGACATGGCA[A/G]GCGCCATGTTGCTCT	3993
rs765906995	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529939	TTTTGACTCGTTCTT[C/T]GCCGAGTCCTTGCTG	3993
rs765936728	snp	C/T	1.74051e-05	0.00294996	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573019	ACGCCCCCAGGTGTT[C/T]ACGCTGCCCAAGGTG	3993
rs765996138	in-del	-/GTCCTTCAGCAGA	1.65146e-05	0.0028735	intron-variant	LLGL2	GRCh38.p7	17:75574862	GAGCTGTCCCTCTGT[-/GTCCTTCAGCAGA]GTGAGTGGCTGAGCG	3993
rs766017181	snp	G/T	1.72392e-05	0.00293586	intron-variant	LLGL2	GRCh38.p7	17:75573449	CTTGGCAGCCGCCAG[G/T]CCAGGCCGCTAGCAT	3993
rs766024427	snp	C/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523241	GAGAAATGTGACTCC[C/T]CTCCCCAGTACCTTG	3993
rs766045873	snp	A/T	3.295e-05	0.00405881	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524349	CTTTGCCCTGGTGGA[A/T]CATGGTGACATCTCC	3993
rs766057821	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75561686	AGCACTTTGGGAGGC[A/G]GAGGCGGGTGGATCA	3993
rs766073577	snp	G/T	3.39991e-05	0.00412291	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569127	AGTGGCCCCCACTCC[G/T]CAAGGTGAGGCCAGG	3993
rs766094794	snp	C/G	0.000105457	0.00726069	intron-variant	LLGL2	GRCh38.p7	17:75570515	TGAGGCCTGAGGTGA[C/G]GCTGCGGCCGGCCAC	3993
rs766114381	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560212	GGATTCCCACTTGGA[A/G]CTGTGTCCCTCTGAG	3993
rs766123925	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75531370	CTATTCGGCCTTCCT[A/G]GTCTTTCCAGATGAG	3993
rs766131458	snp	C/T	1.71519e-05	0.00292842	intron-variant	LLGL2	GRCh38.p7	17:75556008	GTGGCGCGAAGGGGA[C/T]AGGTCTGCAGGCCCA	3993
rs766212281	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75530804	TGACAGAGTGAGACT[C/G]TAACTCAAAAAGAGA	3993
rs766217199	snp	A/G	1.66252e-05	0.00288311	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568644	CGCTGAAGCTGTGGG[A/G]GCGGATCATTGCCGC	3993
rs766217868	snp	G/T	1.78172e-05	0.00298468	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559281	CCACACAGATCACCG[G/T]GGTCCTGCCACATTC	3993
rs766268182	snp	A/G	3.90808e-05	0.00442028	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570069	GGAAGGGGCACGAGC[A/G]CCTGGCAGCCCGCTC	3993
rs766294196	snp	A/G	1.67829e-05	0.00289675	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563114	TGATCGGCTACAGCC[A/G]AGGCCTCGTTGTCAT	3993
rs766432650	snp	C/T			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568040	GTGAGGTGATGTGAT[C/T]GTGTGCAGTAAAGAA	3993
rs766474578	snp	A/G	2.68294e-05	0.00366251	intron-variant	LLGL2	GRCh38.p7	17:75570291	CCCGGGGCTGGGAGT[A/G]GGGCCCGCGAGGACT	3993
rs766498095	snp	A/G/T	3.322e-05	0.00407542	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556125	TGGCCATCGGCACCC[A/G/T]TTCTGGAGCCATCAA	3993
rs766531129	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75535271	CCTCACACAGGATGT[C/T]GCAGAGGGGAAGGCA	3993
rs766531665	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75549241	AGGGCCACTGAGGAC[A/C]AAGGGAAGGAACCAT	3993
rs766542638	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75574042	CCAGACCTGGGGCTG[A/G]ACGGGAGGGAAGGGT	3993
rs766556762	snp	G/T	9.25952e-05	0.0068036	intron-variant	LLGL2	GRCh38.p7	17:75568845	TGCTCACAGGGTAGG[G/T]TACTTTGATGCTACC	3993
rs766613017	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75527053	GTGCACCTGTAGTCC[-/C]AGCTACTCAGGAGCC	3993
rs766620719	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75544676	TCTCCGTGACCTCCC[C/T]GTTGGGAGAGGTGGG	3993
rs766632252	snp	C/T	1.69286e-05	0.0029093	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573516	TCGGAGTTTGAGCGC[C/T]TCTCTCTCTCCACCA	3993
rs766641401	in-del	-/C	1.67364e-05	0.00289274	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556055	TTGCAGACGGTGGAG[-/C]ATGGCTTCCCGCACC	3993
rs766643728	snp	C/G	6.74229e-05	0.00580577	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573206	CTGCTCAAGCCCCAG[C/G]TGCGCTACAGCTGCA	3993
rs766702221	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75528826	AATAGGAGCCCATAG[G/T]GGGAAAAAGGAAACA	3993
rs766721551	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534165	CACTTCCCTGGAGAG[A/G]GAGTCTGGTGTTGGA	3993
rs766770112	snp	A/G	1.76571e-05	0.00297123	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574650	GCCGCCGTGGGGTGC[A/G]GCCTCAGCAATGGCG	3993
rs766776667	in-del	-/CAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75554302	AGCAAAACTCCGTCT[-/CAAAAAA]AAAAAAAAAAAAGCC	3993
rs766811858	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566214	GATGTGGCCAGCGCC[A/G]GATCGTATAGAGCCG	3993
rs766813614	snp	C/G	3.78437e-05	0.00434976	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570193	GTGGCGGCTCGTGGC[C/G]TTCGGCACCAGCCAT	3993
rs766813617	snp	C/T	3.49895e-05	0.00418253	intron-variant	LLGL2	GRCh38.p7	17:75571892	ACACCCACCTCCTCC[C/T]CCTAGCCAAGGAGAT	3993
rs766814727	snp	C/G/T	8.40648e-05	0.00648279	intron-variant	LLGL2	GRCh38.p7	17:75556038	ACCCCACGTGCTTCT[C/G/T]GTTGCAGACGGTGGA	3993
rs766854124	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528263	TGGGACCACAGGCGC[C/T]TGCCATCACGCCCGG	3993
rs766884018	snp	G/T	1.66269e-05	0.00288326	intron-variant	LLGL2	GRCh38.p7	17:75569213	ACAGGGCCCCTCCCC[G/T]TCTCCAGGTGGGCTC	3993
rs766885608	snp	C/G	0.000133307	0.00816306	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564410	CTACGGGGACCGCCA[C/G]TGCATCTCAGTGATC	3993
rs766901869	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567102	AGTTTGGTGGGGATC[G/T]GGCAAAGAACACCTG	3993
rs766936409	snp	G/T	0.000292415	0.0120881	intron-variant	LLGL2	GRCh38.p7	17:75571821	AGAGGGTGCTCGGGC[G/T]GCCTGGGCTGGGTCC	3993
rs766946410	snp	A/G	6.66433e-05	0.00577211	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524470	GGACTGTCTGTTCTC[A/G]GGGACCATCTCGGCT	3993
rs766962464	snp	A/G	1.69086e-05	0.00290758	intron-variant	LLGL2	GRCh38.p7	17:75569143	CAAGGTGAGGCCAGG[A/G]GCCTGGGACCCAGGA	3993
rs766986353	snp	C/G	3.51735e-05	0.00419351	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558530	CAGCTGGTCACCCTG[C/G]TGGATGACAACAGCC	3993
rs767037898	snp	A/G	0.00013985	0.00836096	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573602	CCCTGGTAACGGTGC[A/G]GGCCCCAAGAAGGCC	3993
rs767047115	snp	A/C/G	0.000538428	0.0163991	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564496	TCCTCACAGAGGCAG[A/C/G]CCCTGCAGCCAGTAG	3993
rs767079506	snp	C/T			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575459	TCCCTGGGTCCTGGC[C/T]GCCCCTGGCTGGCCT	3993
rs767126582	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542959	GCCCCGACTTGGGCT[C/T]TGATCTGGGAAGGAT	3993
rs767186932	snp	C/G	1.68077e-05	0.00289889	missense, intron-variant	LLGL2	GRCh38.p7	17:75564514	CTGCAGCCAGTAGGA[C/G]AGCTTCGGGAGTGGG	3993
rs767244006	snp	A/T	4.98542e-05	0.00499245	splice-acceptor-variant	LLGL2	GRCh38.p7	17:75569219	CCCCTCCCCTTCTCC[A/T]GGTGGGCTCCTTTGA	3993
rs767253212	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75553111	TCCCACTGTCTACTC[C/T]CCTTTTCCTGGGAAA	3993
rs767282638	snp	A/G	5.00188e-05	0.00500069	intron-variant	LLGL2	GRCh38.p7	17:75558248	CCAGGTGAGGGACCT[A/G]GGGTGGGACAGGAAG	3993
rs767307471	snp	C/T	4.94181e-05	0.00497057	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523247	TGTGACTCCCCTCCC[C/T]AGTACCTTGTTTTCT	3993
rs767352795	snp	A/G	1.70168e-05	0.00291687	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563354	GAACATCTGGTGGCA[A/G]CGGGACGGCCGCCTG	3993
rs767452053	snp	C/T	1.66374e-05	0.00288417	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568651	GCTGTGGGAGCGGAT[C/T]ATTGCCGCCGGCAGC	3993
rs767502643	snp	C/T	1.69444e-05	0.00291066	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573037	GCTGCCCAAGGTGAG[C/T]GCCAAGCTGAAGTTG	3993
rs767540136	snp	C/G	4.94442e-05	0.00497188	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523619	TGGAAAAGAAAGGTT[C/G]GGGAGAAGAGTTCAT	3993
rs767542225	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536243	CAGTGACCATTTCTG[A/G]TGTTAGACTTGAGGA	3993
rs767602142	snp	C/G	0.000145317	0.00852276	intron-variant	LLGL2	GRCh38.p7	17:75558663	CCCTTCCACTCCCAG[C/G]CCAGCCTGACCCTTG	3993
rs767613520	snp	A/G	8.38553e-05	0.00647461	intron-variant	LLGL2	GRCh38.p7	17:75568714	TCTGGCCCTGGCCCC[A/G]GCCCCAGCCCCACCG	3993
rs767619194	snp	A/G	1.84096e-05	0.00303389	intron-variant	LLGL2	GRCh38.p7	17:75568959	CCTCTCACGCCTGGC[A/G]GGTGGGTTCTGCCCA	3993
rs767630772	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566902	TTCAGAGGAGAGATC[A/G]GGAAGGTGTCCATTT	3993
rs767631739	snp	C/T	0.000131796	0.00811668	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524283	TGAGCCTGTCCCAGA[C/T]CTCTGCAGCCTCAAG	3993
rs767660585	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572863	GAAGTCGGTGACCTC[A/G]GCATCCTCCCAGGCC	3993
rs767683134	snp	C/T	3.38484e-05	0.00411376	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573218	CAGGTGCGCTACAGC[C/T]GCATCCGCCGGGAGG	3993
rs767683456	snp	C/T	1.65745e-05	0.00287871	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523730	GACGCTGTGGCCACA[C/T]TCCGAAAGAATAACC	3993
rs767684174	snp	A/G	6.62295e-05	0.00575416	intron-variant	LLGL2	GRCh38.p7	17:75563714	GACACTTGTCTGAGA[A/G]TTTGAGGATCCGTTC	3993
rs767697295	in-del	-/GCT	1.65168e-05	0.00287369	cds-indel, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558184	CGTGGAGTTCATGGG[-/GCT]GCTGCACCAGGAGAA	3993
rs767751540	snp	C/T	1.71637e-05	0.00292943	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571920	GATCCAGCTGATGCA[C/T]CGGGCGCCGGTGGTG	3993
rs767783013	snp	C/G	3.43519e-05	0.00414424	intron-variant	LLGL2	GRCh38.p7	17:75571647	TAAGGGTCAGACACC[C/G]AAACATGGCTTCTCG	3993
rs767817766	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75530647	AGAGCGAGACTCCAT[-/T]TCAAAAAAAAAAAAA	3993
rs767884155	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75539030	CCCAAGTAGCTGGGA[C/G]CACAGGTGCTTGACA	3993
rs767906027	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75531663	GGCAGGAGACGGGCG[-/T]TCCCCCAGCGGGGCC	3993
rs767922390	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541939	TTTCACCATGTTGGC[C/T]AGGCTGGTCTCAAAC	3993
rs767945152	snp	A/C/T	0.000137315	0.008285	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563032	TTGCCAGAGGAGGCC[A/C/T]GCCACCGGCGTGTGT	3993
rs767958810	snp	A/G	1.65318e-05	0.002875	intron-variant	LLGL2	GRCh38.p7	17:75568863	CTTTGATGCTACCCC[A/G]CCTCTTCCCAGTAGG	3993
rs768013530	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542805	GTGCTCTGTGCCACC[C/T]GTGCCCACTTGAGTT	3993
rs768022991	snp	C/T	1.74683e-05	0.00295531	intron-variant	LLGL2	GRCh38.p7	17:75559416	TGCTGCAGCGGTGAG[C/T]CCAGAGCCCAGCTGC	3993
rs768031262	snp	A/G	3.54384e-05	0.00420927	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574662	TGCAGCCTCAGCAAT[A/G]GCGGAGGTGGGGGCT	3993
rs768081477	snp	C/T	0.000181745	0.00953097	intron-variant	LLGL2	GRCh38.p7	17:75570299	TGGGAGTGGGGCCCG[C/T]GAGGACTCCCAGGAC	3993
rs768112797	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75570887	AGGATCAGCACTGAG[C/T]GAAGCACTGTTCCTG	3993
rs768133300	snp	C/G	2.82346e-05	0.0037572	intron-variant	LLGL2	GRCh38.p7	17:75558002	GCTGTGTCTCCTCCC[C/G]ACCCTAGGCTCCATG	3993
rs768139605	snp	C/T	5.08703e-05	0.00504307	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571966	GACGGACACAGCGTA[C/T]CCCTTCCCGAGCCCC	3993
rs768201668	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75530650	GCGAGACTCCATTTC[-/AA]AAAAAAAAAAAAAAA	3993
rs768245673	snp	A/G	8.85445e-05	0.00665315	intron-variant	LLGL2	GRCh38.p7	17:75559236	GTCGGCTCACGGGCA[A/G]CTGTTCTTGTCACAG	3993
rs768268682	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75536341	ACTTAAGTGCACAGC[-/A]CCTGAGAGTTTGCCA	3993
rs768310566	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75565468	TCTTTCTTTCTCAGC[C/G]TCTCCTCCCTCCTCA	3993
rs768333569	snp	A/G	4.79582e-05	0.00489661	intron-variant	LLGL2	GRCh38.p7	17:75558645	AAGGGCTCAATCCCC[A/G]GCCCCTTCCACTCCC	3993
rs768335688	snp	A/G	1.65261e-05	0.0028745	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563781	AAAGCGATTACCAGA[A/G]TCCTCTGGCTGACCA	3993
rs768343130	snp	A/G	9.42782e-05	0.00686515	intron-variant	LLGL2	GRCh38.p7	17:75569959	CACCTGCCACCCTGC[A/G]CAGGTGCTGGTACTG	3993
rs768353801	snp	C/T	0.000101261	0.00711478	intron-variant	LLGL2	GRCh38.p7	17:75573987	ATGGCGAGGGTAAGA[C/T]AGGCCTCCTGGGCTC	3993
rs768398207	snp	A/C	1.6492e-05	0.00287154	synonymous-codon, stop-gained, upstream-variant-2KB, intron-variant, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523693	TGGGGGCTTGGAAAT[A/C]ATCTTTGATGTTTAC	3993
rs768419209	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75530600	GCTGGCAGTGAGCCG[A/G]GATCGCGCCACTGCA	3993
rs768484488	snp	C/T	3.51241e-05	0.00419056	intron-variant	LLGL2	GRCh38.p7	17:75557973	CACTGGCCTGGTGCC[C/T]CAGGGCCAGGGCTGC	3993
rs768499109	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75536042	CTTTTGCGGCCCGGC[A/T]CTAAACCCTGGCGCC	3993
rs768583575	snp	A/G	1.71749e-05	0.00293038	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573242	CGGGAGGACGTCAGT[A/G]GCATCGCCTCCTGCG	3993
rs768598746	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536605	CTGGACCCACCCTCC[C/T]GCCTGACCATGCCTG	3993
rs768614595	in-del	-/GTGGGCCCGAGGCTCTGCCA	7.75164e-05	0.00622512	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574522	CCCAGGCCAGCTGGG[-/GTGGGCCCGAGGCTCTGCCA]GAGGGCTCAGGGGAG	3993
rs768620901	snp	C/T	1.70368e-05	0.00291858	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569110	TGCCCAGGGCGAGGA[C/T]GAGTGGCCCCCACTC	3993
rs768661779	snp	G/T	3.32038e-05	0.00407441	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558232	TCCACCTCCTGCCCG[G/T]CCAGGTGAGGGACCT	3993
rs768667174	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75548522	GCCAAAGAAGTGGCC[A/G]GGCGCCGTGTCTCCT	3993
rs768680627	snp	C/T	1.71167e-05	0.00292542	intron-variant	LLGL2	GRCh38.p7	17:75563494	GCCGGGCAGGGCCCA[C/T]CCCCAGTGCCTCCTG	3993
rs768684459	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75545650	GGGCCTGATCTGACC[C/T]TGCGGCTCCAGGGGT	3993
rs768706544	snp	A/T	1.7095e-05	0.00292356	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573562	CCCGGTGTCTGGTGG[A/T]TTCAGCAGAAACCAA	3993
rs768710079	snp	A/C/G	0.000147091	0.00857477	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574703	GTGCAGCTGCCAACC[A/C/G]TGCTGGGAAGGGCTG	3993
rs768732593	snp	C/T	1.66341e-05	0.00288388	intron-variant	LLGL2	GRCh38.p7	17:75569185	CAGCTGGGTCCTGTC[C/T]CCGTGGCTGCTCACA	3993
rs768739006	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75549526	TGCGGAGGGCCAGGT[G/T]GTTCTGTATTGGCTT	3993
rs768781065	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75556740	AGGGACCCCTCTTGT[C/T]GCTAGGGATGTTTTT	3993
rs768781787	snp	A/C	1.8333e-05	0.00302757	intron-variant	LLGL2	GRCh38.p7	17:75570926	AGTCCAGAGCTGACC[A/C]TTAGGCTGGCCCACC	3993
rs768834216	snp	C/T	3.34191e-05	0.0040876	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564470	CACCTCCCGTGTCAT[C/T]GGCTTCACTGTCCTC	3993
rs768855175	in-del	-/GGCCAG			intron-variant	LLGL2	GRCh38.p7	17:75537028	GGGTTTTGGCATGTT[-/GGCCAG]GCTGCTCGCAAACTC	3993
rs768869598	snp	A/G	1.70467e-05	0.00291943	intron-variant	LLGL2	GRCh38.p7	17:75571798	GGTGAGTGCTGGGCA[A/G]GGAGAGCAGAGGGTG	3993
rs768909655	in-del	-/TG			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566071	CGTATTTGCGCAGAC[-/TG]ACGGAAGCAGTCTGA	3993
rs768932278	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75538961	GCAGTGGTACAGTCA[G/T]AGCTCACAGCAGCCT	3993
rs768986085	snp	A/C/T	3.38778e-05	0.00411557	stop-gained, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573502	ACCTGATCTCACCCT[A/C/T]GGAGTTTGAGCGCTT	3993
rs769009795	snp	C/G	3.90396e-05	0.00441795	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524509	TACCCAGACTCTAAC[C/G]TGTAGCTTCAGAGGC	3993
rs769021250	in-del	-/CAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75550780	AGTGAGACCCTGTCT[-/CAAAAA]AAAAAAAAAAAAAAA	3993
rs769022823	snp	C/T	1.68363e-05	0.00290136	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563167	GTGCTCTACCACTTC[C/T]TCAGCAGCCAGGTAG	3993
rs769027586	snp	A/G	1.71838e-05	0.00293114	intron-variant, synonymous-codon	LLGL2	GRCh38.p7	17:75570504	CCCAGGAGAGGTGAG[A/G]CCTGAGGTGAGGCTG	3993
rs769075767	snp	A/G	3.32878e-05	0.00407956	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568616	ACCTGCTCTCACCAC[A/G]TCTCCAACATCCCGC	3993
rs769169058	snp	C/T	0.000238521	0.010918	synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574241	CCTGGTGATGGAGCG[C/T]GCTCTGCTCAGTGAT	3993
rs769229816	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532950	GTGATTGGCAGATAC[C/T]TTTTCTAGTTAATCC	3993
rs769270783	snp	C/G	1.78557e-05	0.0029879	intron-variant	LLGL2	GRCh38.p7	17:75573002	GCATGAACAACCACC[C/G]CACGCCCCCAGGTGT	3993
rs769275439	snp	C/T	1.65135e-05	0.00287341	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558164	TCCTAGCTACGGAGC[C/T]CCAGGCGTGGAGTTC	3993
rs769340246	snp	C/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523224	AAACTAGATGGCAGA[C/T]TGAGAAATGTGACTC	3993
rs769349711	snp	A/G/T	5.71852e-05	0.00534695	missense, stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570065	CGCTGGAAGGGGCAC[A/G/T]AGCGCCTGGCAGCCC	3993
rs769387744	snp	A/G	1.6743e-05	0.0028933	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556051	CTCGTTGCAGACGGT[A/G]GAGCATGGCTTCCCG	3993
rs769401352	snp	G/T	0.00217249	0.0328866	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574299	GGCTGGCAGGAGGGG[G/T]GGGGAAGGGGGGTCA	3993
rs769401516	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75535904	AGACGTGGGTGAGTG[A/G]AACAGTGAGGAGGGA	3993
rs769429997	snp	C/T	1.65296e-05	0.00287481	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563791	CCAGAATCCTCTGGC[C/T]GACCACTAGGCAGGG	3993
rs769435036	snp	C/G	1.66416e-05	0.00288453	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568686	AGAACGCACACTTCT[C/G]CACCATGGTAGGTCT	3993
rs769465906	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75543689	AGGGGAATAGGTTGC[C/T]CTCATGAGTTGGGAC	3993
rs769516106	snp	C/T	3.30387e-05	0.00406427	intron-variant	LLGL2	GRCh38.p7	17:75558145	AGAGCTTTCCTGAGC[C/T]TACTCCTAGCTACGG	3993
rs769529029	snp	A/G	6.59055e-05	0.00574007	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524270	CCTGCAGATTTGATG[A/G]GCCTGTCCCAGACCT	3993
rs769564754	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545365	CCAAGGCTCAGGGCT[A/G]TGGGAATCTGATTAG	3993
rs769584328	snp	C/T	1.66635e-05	0.00288643	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556099	CGGCTACAGCCCGTC[C/T]CTGCGCATCCTGGCC	3993
rs769589925	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567539	AGCTACTTGGGAAGC[A/T]GAGGCAGGAGAATCG	3993
rs769628537	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75573761	ACCCTCCCAGGCTCC[A/G]GCTCTCCTTGCCTCT	3993
rs769736551	snp	A/C	1.65214e-05	0.0028741	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574916	CGATGAGCACACACT[A/C]CTACTGATGGCCTTT	3993
rs769772644	snp	A/C/G	6.71123e-05	0.00579243	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564480	GTCATCGGCTTCACT[A/C/G]TCCTCACAGAGGCAG	3993
rs769800912	snp	C/G	9.77406e-05	0.00699004	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524544	CTGGGCCTTGGCCCT[C/G]GGTGTCTGATACTCA	3993
rs769841661	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537212	CATTTAGGTTGCTTC[C/T]GATTTTTTCTGACAG	3993
rs769847017	snp	A/C	1.94945e-05	0.003122	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559259	TGTCACAGGGCTGCC[A/C]CCAGTGCCACACAGA	3993
rs769910664	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75556573	TTTTGCAGGGGTTGT[A/G]TTGGTGGATCCAGAG	3993
rs769989122	snp	A/G	1.69778e-05	0.00291352	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571951	GGCATCCTGGTGCTC[A/G]ACGGACACAGCGTAC	3993
rs770000521	snp	A/G	4.97682e-05	0.00498815	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569261	ATGACCCCCGGCTGG[A/G]CATCCAGAAGATCTT	3993
rs770039948	snp	A/T	1.65756e-05	0.00287881	intron-variant	LLGL2	GRCh38.p7	17:75570271	GTGAGCAGGGGCGGC[A/T]GGGTCCCGGGGCTGG	3993
rs770044438	snp	A/G	1.86433e-05	0.00305308	intron-variant	LLGL2	GRCh38.p7	17:75573643	CCAGGTGAGTGAAAG[A/G]GCCAGAGGCCTCTCC	3993
rs770106688	in-del	-/CTT	1.6998e-05	0.00291525	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543382	AGACCCCTGCAGCTC[-/CTT]CTGTTTCTCCAGGTC	3993
rs770107992	snp	A/G	8.4827e-05	0.00651201	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563388	GTCAGCTGTCACTCT[A/G]ACGGCAGCTACTGCC	3993
rs770125612	snp	C/T	1.67638e-05	0.0028951	intron-variant	LLGL2	GRCh38.p7	17:75558257	GGACCTGGGGTGGGA[C/T]AGGAAGCCACTTCCA	3993
rs770184510	snp	C/T	6.43107e-05	0.00567021	intron-variant	LLGL2	GRCh38.p7	17:75558502	TGATCCCGTCGTGTG[C/T]CCTCGCCAGTGCCAG	3993
rs770227594	snp	C/T	3.37741e-05	0.00410925	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573086	GGCTCAAGAGTGCGG[C/T]GGGTCAGCGTGGCCC	3993
rs770238073	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75527404	AGACTGGGCCCATCT[C/T]TGTGGGGGCTCCTGG	3993
rs770256587	snp	A/G	3.29473e-05	0.00405864	missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523323	CAACACACCTTCCTG[A/G]TGGAGGTGCCCGGTA	3993
rs770293309	in-del	-/CAA	0.000174581	0.00934131	cds-indel, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569080	CACCGACACGGACCC[-/CAA]CGAGAACTTCAGTGC	3993
rs770294483	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75562663	AACCTCCGCCTCCTG[A/G]GTTCAAGCAATTCTC	3993
rs770298823	snp	A/G	8.74378e-05	0.00661145	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568780	TTTCTAGGAGTGGCC[A/G]ATTGATGGTGGCACC	3993
rs770311518	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75552874	CCGTTCTGGGCAGCT[C/T]GGAGCATGGGGCCTG	3993
rs770314814	in-del	AAAAAAACAAAG/GA			intron-variant	LLGL2	GRCh38.p7	17:75560826	AAAAAAAAAAAAAAA[AAAAAAACAAAG/GA]AAAAAACATTTTTTT	3993
rs770317928	snp	A/G	1.65002e-05	0.00287225	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524435	GCTCTGCAGAGGATG[A/G]AGCTTGCTCCGGGGG	3993
rs770365819	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75534564	TAGCTCACTGCAGCC[G/T]CAACCTCCTGGGCTC	3993
rs770398163	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542043	GCGATTTTGTAAAAT[C/T]GGGTCACCCTCCCAG	3993
rs770416532	snp	C/T	1.66352e-05	0.00288398	intron-variant	LLGL2	GRCh38.p7	17:75569196	TGTCCCCGTGGCTGC[C/T]CACAGGGCCCCTCCC	3993
rs770433556	snp	C/T	1.79664e-05	0.00299714	intron-variant	LLGL2	GRCh38.p7	17:75570943	TAGGCTGGCCCACCC[C/T]TTGCAGGCACAGGAG	3993
rs770460425	snp	C/G	1.69484e-05	0.002911	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563395	GTCACTCTGACGGCA[C/G]CTACTGCCAGTGGCC	3993
rs770471325	snp	C/T	1.81023e-05	0.00300846	intron-variant	LLGL2	GRCh38.p7	17:75570938	ACCCTTAGGCTGGCC[C/T]ACCCCTTGCAGGCAC	3993
rs770481002	snp	C/T	1.66665e-05	0.00288669	splice-donor-variant	LLGL2	GRCh38.p7	17:75568695	ACTTCTCCACCATGG[C/T]AGGTCTGGCCCTGGC	3993
rs770556188	snp	G/T	1.69066e-05	0.00290741	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573093	GAGTGCGGCGGGTCA[G/T]CGTGGCCCACTTCGG	3993
rs770558755	snp	A/G	5.0452e-05	0.00502229	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573135	CCGAGGACTACGGGG[A/G]GCACCACCTGGCAGT	3993
rs770564636	snp	A/G	3.33589e-05	0.00408391	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559335	GCACCGAGAGTGGCA[A/G]CGTGTTTGTGGTGCA	3993
rs770573752	snp	A/C/T	8.69334e-05	0.00659245	synonymous-codon, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570239	GACCACCAGCAGCGG[A/C/T]GGCAGGTCTTTGTTA	3993
rs770576019	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75565408	CTGGTCTGTGTACTC[-/A]ACGGCCTCTATCTAC	3993
rs770591447	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75544384	GGCTCCCCTGCCCCC[G/T]AAAGGAAGCAGTGGA	3993
rs770633592	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75533593	GCAGGCATGAGCCAC[C/T]GCGCCCAGCCCGTTC	3993
rs770652451	snp	A/C	0.000101707	0.00713044	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573497	CTTCTACCTGATCTC[A/C]CCCTCGGAGTTTGAG	3993
rs770672246	snp	C/T	4.99189e-05	0.00499569	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564455	GACGGCCTTCGACTT[C/T]ACCTCCCGTGTCATC	3993
rs770699353	snp	A/G	0.000115337	0.00759312	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524388	CTTCAGGGACTTCAC[A/G]TTGCCCCAGGATGTG	3993
rs770702308	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566852	GACCCATAAGGGAGA[C/T]GCTGAGTAGACAACT	3993
rs770715016	snp	C/T	3.29647e-05	0.00405971	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523644	GTTCATGTCATAACG[C/T]TTCTCATTGTATTGT	3993
rs770722602	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555669	GAGACCGGTGTCTCC[A/G]TTGTTCCAAACTCCC	3993
rs770727300	snp	A/T	1.73676e-05	0.00294678	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564354	TCTGTGCCTGCCAGG[A/T]TGCCCTTCACCATCT	3993
rs770783119	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75554145	CATCTCTACTGAAAA[C/T]ACAAAAATTAGCTGG	3993
rs770854421	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75533974	AATCCCCACCTCCTG[G/T]AGCTGACATCTGGAA	3993
rs770984675	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566037	AGACAAGGGTTGGCA[A/G]GGCCTCCCTGATAAG	3993
rs770996592	in-del	-/TC			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524461	GGGGGACCGGGACTG[-/TC]TGTTCTCAGGGACCA	3993
rs771004471	snp	C/T	1.67854e-05	0.00289697	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563079	ACTGCAGGAGCACCC[C/T]CGAGACCCCAACCAG	3993
rs771033746	snp	C/T	1.69519e-05	0.0029113	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571775	ATGAGCCTGTGCGGG[C/T]AGAGCAGGGTGAGTG	3993
rs771086432	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542755	ACCGGCAGAGACCCC[A/G]GGCACGGTGGCATGG	3993
rs771130362	snp	C/T	3.29799e-05	0.00406065	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570445	TCATTCCGCCGGATG[C/T]GTCGGAGCCGGGTGT	3993
rs771149902	snp	C/T	1.68909e-05	0.00290606	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568503	CCTATGCCCTGGTGG[C/T]GCTGGCTGAGGAGGA	3993
rs771183463	snp	A/G	1.7129e-05	0.00292647	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572017	TCGAAGAGCCCTGAC[A/G]TGCAGGGAAGCCACC	3993
rs771211459	snp	A/C	1.85824e-05	0.00304809	intron-variant	LLGL2	GRCh38.p7	17:75574712	CCAACCGTGCTGGGA[A/C]GGGCTGGGAGGAAGA	3993
rs771220620	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529852	GTGACAGAGCAAGAC[C/T]CCGTCTCAAACTAAT	3993
rs771244483	snp	C/G	3.49773e-05	0.00418179	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524578	AGTGAAACTGTGACC[C/G]TCTCCCTTCCCTGCT	3993
rs771275706	snp	C/T	8.62627e-05	0.00656688	intron-variant	LLGL2	GRCh38.p7	17:75573655	AAGGGCCAGAGGCCT[C/T]TCCCGCCCCTCCCGC	3993
rs771332820	snp	A/G	5.55942e-05	0.005272	splice-acceptor-variant	LLGL2	GRCh38.p7	17:75558510	TCGTGTGCCCTCGCC[A/G]GTGCCAGCTGGTCAC	3993
rs771374490	in-del	-/AAAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75550781	GTGAGACCCTGTCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA	3993
rs771407934	in-del	-/GCTGGGGAGGGGGA	1.70571e-05	0.00292032	intron-variant	LLGL2	GRCh38.p7	17:75569338	CAGGTAGCAGGCTGG[-/GCTGGGGAGGGGGA]GCTGGGGAGGAGTGG	3993
rs771473369	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562208	GCAGGGGTCAAGGCT[C/T]CAGGGCCAGGCCAAC	3993
rs771473455	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524088	TTGCTCTTCCTAGCA[C/T]CTCCCCAACCAGTGC	3993
rs771508231	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75544281	GCTGCAGGAACTGGG[A/C]CACTGTGATCCTCTT	3993
rs771538343	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75550700	TCAGGTGGATCACTT[C/G]AGCCCGGGAGGAGGA	3993
rs771561533	in-del	-/CCTCCTGTACC	1.72015e-05	0.00293265	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524486	GGACCATCTCGGCTG[-/CCTCCTGTACC]CCTCCTGTACCCAGA	3993
rs771611240	snp	C/T	3.72974e-05	0.00431825	intron-variant	LLGL2	GRCh38.p7	17:75558635	CCCCCAGGGTAAGGG[C/T]TCAATCCCCAGCCCC	3993
rs771615987	snp	C/T	4.99846e-05	0.00499898	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569292	CCTCTGCAAGTACAG[C/T]GGCTACCTGGCTGTG	3993
rs771620067	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551508	GGGAGGGGTGGCCAC[A/G]ATAACTCCAAGGCTT	3993
rs771702625	snp	A/C	7.44921e-05	0.0061025	intron-variant	LLGL2	GRCh38.p7	17:75571150	TAGTGGGCAGCAGAC[A/C]CCCCCTGACCTGGGG	3993
rs771720511	snp	A/G	1.93936e-05	0.00311391	intron-variant	LLGL2	GRCh38.p7	17:75568926	ACGAGCCAGCCCCTG[A/G]GCATCCCGGCTGGCA	3993
rs771755888	snp	A/G	3.35188e-05	0.00409369	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571032	GCAAGATCGAGGCTC[A/G]CTCGGCAGAGGACTC	3993
rs771774032	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75543605	GTATAGCTCTTATGT[A/G]ACTGCCTGCAGTGCC	3993
rs771779671	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75548308	TTTGGACGGAGTTTA[A/G]CTCTTGTTGCCCGGG	3993
rs771849324	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75527876	CACTGCAGACTCGAC[C/T]TCCCAGGCTCAAGTG	3993
rs771917520	snp	C/G	1.64749e-05	0.00287005	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523344	GTGCCCGGTAAGTTT[C/G]CAAGCAGTGCCGTCT	3993
rs771933197	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526274	AGCCCCTGCCCCTGC[C/T]ATCTGGGCTGTGTCC	3993
rs771972860	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75536741	TACATTGTCAAATAT[A/G]GGGATTTTTAATAGA	3993
rs772079289	snp	A/G	7.13318e-05	0.00597167	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570455	GGATGCGTCGGAGCC[A/G]GGTGTCCAGCCGGAA	3993
rs772082716	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75529808	GGAGGTTGCAGTGAG[C/T]CGAGATCGCGCCACT	3993
rs772089563	in-del	-/G	2.58368e-05	0.00359412	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570422	CCTCAAGAAGTCCTT[-/G]GCGTCAGTCATTCCG	3993
rs772127160	snp	C/T	2.15153e-05	0.00327982	intron-variant	LLGL2	GRCh38.p7	17:75570339	CTGACAGCCTGCCAT[C/T]CCCCCAAGGTGCACA	3993
rs772129153	snp	A/G	1.76874e-05	0.00297378	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568801	TGGTGGCACCAGCCT[A/G]ACCCCAGCCCCACCC	3993
rs772182323	snp	C/G	2.80619e-05	0.00374569	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570247	GCAGCGGCGGCAGGT[C/G]TTTGTTAAGTGAGCA	3993
rs772228755	snp	C/T	1.81424e-05	0.00301179	intron-variant	LLGL2	GRCh38.p7	17:75572982	GAGAACTGGTTTGGC[C/T]ATGGGCATGAACAAC	3993
rs772239392	snp	A/T	1.65157e-05	0.0028736	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558157	AGCCTACTCCTAGCT[A/T]CGGAGCCCCAGGCGT	3993
rs772271930	in-del	-/CTCCCGCCC	0.000149893	0.00865587	intron-variant	LLGL2	GRCh38.p7	17:75573655	AAGGGCCAGAGGCCT[-/CTCCCGCCC]CTCCCGCCCCTCCCT	3993
rs772318830	snp	C/T			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551377	AAGCTCAGGGAGGCC[C/T]AGCAGCTCATCCACG	3993
rs772335625	snp	A/G	1.68103e-05	0.00289911	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563150	ACCTACAGGGCAGCC[A/G]CGTGCTCTACCACTT	3993
rs772381661	snp	C/T	1.72788e-05	0.00293923	intron-variant	LLGL2	GRCh38.p7	17:75555997	CAGCAGCCATGGTGG[C/T]GCGAAGGGGACAGGT	3993
rs772390170	snp	C/G	1.69746e-05	0.00291325	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570490	CACCCGGCTGGCCCC[C/G]CAGGAGAGGTGAGGC	3993
rs772403669	snp	A/G	1.80117e-05	0.00300092	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572062	TCAGAGGAGCAGTTC[A/G]AGGTGCCACACGGGC	3993
rs772408855	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541460	CTTTCCCAGCCGGTG[C/G]CTGTTCTCTGAACCC	3993
rs772435141	snp	G/T	1.67961e-05	0.00289789	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568525	TGAGGAGGAGCTGGT[G/T]GTGATTGACCTGCAG	3993
rs772466388	snp	G/T	1.66799e-05	0.00288785	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543492	GCGGGACCTGTTCCA[G/T]TTTAACAAGGTAAGT	3993
rs772492157	snp	A/C	1.90333e-05	0.00308485	intron-variant	LLGL2	GRCh38.p7	17:75569951	TGCTGAGCCACCTGC[A/C]ACCCTGCGCAGGTGC	3993
rs772530615	snp	A/G	0.000260032	0.0113995	intron-variant	LLGL2	GRCh38.p7	17:75559224	TGCTGGGCAGTGGTC[A/G]GCTCACGGGCAGCTG	3993
rs772540810	snp	A/C/G	0.0034674	0.041503	intron-variant	LLGL2	GRCh38.p7	17:75573660	CCAGAGGCCTCTCCC[A/C/G]CCCCTCCCGCCCCTC	3993
rs772640424	snp	A/G	0.000408497	0.0142857	intron-variant	LLGL2	GRCh38.p7	17:75574024	ACCTGGGCCACACCC[A/G]GCCCAGACCTGGGGC	3993
rs772675552	snp	A/G	1.67581e-05	0.00289461	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563090	ACCCTCGAGACCCCA[A/G]CCAGATCCTGATCGG	3993
rs772680810	snp	C/T	1.66327e-05	0.00288376	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568640	ATCCCGCTGAAGCTG[C/T]GGGAGCGGATCATTG	3993
rs772700073	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75561499	GGGCAAGGCGGCACA[C/T]GTCTGCAGTCTCAGC	3993
rs772718372	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75562530	TCTGTCTTGTTCTAC[A/G]TGCTGCCCTTCTCCC	3993
rs772747700	snp	C/G/T	3.34622e-05	0.00409023	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570149	TGTCAGCCCCCGGCT[C/G/T]TGGTCACCTCCTTGG	3993
rs772757600	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75533682	GCAAAGATGTCTGCC[A/G]TCGTTGAAAGTTGTT	3993
rs772788673	snp	A/C	1.71602e-05	0.00292913	intron-variant	LLGL2	GRCh38.p7	17:75563310	CGTGCTGCCCTCTGT[A/C]CCTCTCCTCTTCCTC	3993
rs772853182	snp	A/G			synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556054	GTTGCAGACGGTGGA[A/G]CATGGCTTCCCGCAC	3993
rs772910657	snp	C/G	1.69421e-05	0.00291046	intron-variant	LLGL2	GRCh38.p7	17:75563190	CCAGGTAGGCAGTGC[C/G]CAGGACATGGCAGGC	3993
rs772914725	in-del	-/CAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75550780	AGTGAGACCCTGTCT[-/CAAAAAA]AAAAAAAAAAAAAAA	3993
rs772924717	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75572375	CAAAAAAAAATAGCC[C/T]GGCATGGGCCAGGCG	3993
rs772950476	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75554105	TCAAGAGTTCAAGAC[C/G]AGCCTGGCCAACATG	3993
rs772972859	snp	A/G	1.66902e-05	0.00288874	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559331	CTGGGCACCGAGAGT[A/G]GCAACGTGTTTGTGG	3993
rs772979528	snp	A/G	1.66479e-05	0.00288508	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568688	AACGCACACTTCTCC[A/G]CCATGGTAGGTCTGG	3993
rs772986299	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75548908	TGCCTGACACAGGTC[A/G]ACGCCTTACCAGGAC	3993
rs773040901	snp	A/C/G/T	4.95925e-05	0.0049794	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563794	GAATCCTCTGGCTGA[A/C/G/T]CACTAGGCAGGGGTA	3993
rs773055135	snp	A/C	5.17531e-05	0.00508664	intron-variant	LLGL2	GRCh38.p7	17:75571633	CCCGACTCCCACGCT[A/C]AGGGTCAGACACCCA	3993
rs773110264	snp	C/T	4.96159e-05	0.00498051	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574932	CTACTGATGGCCTTT[C/T]GGGGGTCCCTGCCCC	3993
rs773146493	snp	C/T	1.73918e-05	0.00294883	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564553	GTTAGGTGTGGGAGG[C/T]ATGGGGCAGGACCAT	3993
rs773154810	in-del	-/C			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523800	AGTGAGCCAGCACTG[-/C]CCCCTCCCCCAGCTG	3993
rs773157593	snp	C/T			utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564678	GTCCAGCCTGGACAA[C/T]GTAGGGAGACCCTTG	3993
rs773191139	snp	G/T	1.74281e-05	0.00295191	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573251	GTCAGTGGCATCGCC[G/T]CCTGCGTCTTCACCA	3993
rs773208858	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75551820	TAATTATTTAAACAC[A/G]TGAAATTAATTTTAA	3993
rs773239055	snp	C/T	3.77302e-05	0.00434323	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559266	GGGCTGCCCCCAGTG[C/T]CACACAGATCACCGT	3993
rs773265849	snp	A/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567741	GAGCCCAGGAGTTCA[A/T]CACCAGCCTGAGCAA	3993
rs773274254	snp	C/T	7.03829e-05	0.00593182	intron-variant	LLGL2	GRCh38.p7	17:75571885	AGCCCCAACACCCAC[C/T]TCCTCCCCCTAGCCA	3993
rs773312603	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529810	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	3993
rs773318892	snp	C/T	5.50449e-05	0.00524589	intron-variant	LLGL2	GRCh38.p7	17:75570278	GGGGCGGCTGGGTCC[C/T]GGGGCTGGGAGTGGG	3993
rs773330217	snp	C/T	1.72722e-05	0.00293867	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573588	ACCAAGAACCACCGC[C/T]CTGGTAACGGTGCGG	3993
rs773360042	snp	C/T	1.72546e-05	0.00293718	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559404	GCTCGGACGCGGTGC[C/T]GCAGCGGTGAGCCCA	3993
rs773369162	snp	A/G/T	0.000200211	0.0100036	intron-variant	LLGL2	GRCh38.p7	17:75557984	TGCCCCAGGGCCAGG[A/G/T]CTGCTGTGTCTCCTC	3993
rs773377866	snp	C/T	3.51241e-05	0.00419056	intron-variant	LLGL2	GRCh38.p7	17:75562997	GGCATCGGAGGCTCA[C/T]GGCACTCCCCTCGCC	3993
rs773386580	in-del	-/ACAC			intron-variant	LLGL2	GRCh38.p7	17:75545989	CAGTAGCACATACAT[-/ACAC]ACACAGCCTGTCAAG	3993
rs773407063	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75557797	TGATAGGCCCCCTGG[A/G]GTGCCGTGTGTTTTT	3993
rs773436115	snp	C/T	8.48644e-05	0.00651345	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571953	CATCCTGGTGCTCGA[C/T]GGACACAGCGTACCC	3993
rs773441984	snp	C/G	6.36072e-05	0.00563911	intron-variant	LLGL2	GRCh38.p7	17:75570344	AGCCTGCCATCCCCC[C/G]AAGGTGCACACTGCA	3993
rs773459946	snp	A/G	0.00691389	0.0583879	intron-variant	LLGL2	GRCh38.p7	17:75558260	CCTGGGGTGGGACAG[A/G]AAGCCACTTCCATGC	3993
rs773470769	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528686	GAGGTTGCGGTGAGC[C/T]AAGATCACGCCATTG	3993
rs773575464	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75539394	ATTGTTCCATGTAAA[-/T]TTGAAAAAATGTCCT	3993
rs773638142	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567015	CTGATGAGGCTGCCC[A/G]GGTGGTAAGGAAGAC	3993
rs773655993	snp	C/T	0.000297447	0.0121916	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524444	AGGATGGAGCTTGCT[C/T]CGGGGGACCGGGACT	3993
rs773670870	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75540112	AGCTATGCGGTGCTG[C/T]GATGGTGAGCCCTGG	3993
rs773677899	snp	C/T	3.39905e-05	0.00412239	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569120	GAGGACGAGTGGCCC[C/T]CACTCCGCAAGGTGA	3993
rs773679914	snp	A/C	1.80634e-05	0.00300523	intron-variant	LLGL2	GRCh38.p7	17:75570939	CCCTTAGGCTGGCCC[A/C]CCCCTTGCAGGCACA	3993
rs773713307	snp	A/G	1.70177e-05	0.00291694	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563348	ACTGGAGAACATCTG[A/G]TGGCAGCGGGACGGC	3993
rs773727088	in-del	-/AAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75550782	TGAGACCCTGTCTCA[-/AAAAAAA]AAAAAAAAAAAAAAA	3993
rs773746567	snp	A/G/T	0.000109214	0.00738898	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524566	TGATACTCACAGAGT[A/G/T]AAACTGTGACCCTCT	3993
rs773786152	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562637	GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT	3993
rs773836919	snp	A/G	6.76041e-05	0.00581356	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573095	GTGCGGCGGGTCAGC[A/G]TGGCCCACTTCGGCA	3993
rs773891537	snp	C/T	3.50097e-05	0.00418373	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568782	TCTAGGAGTGGCCAA[C/T]TGATGGTGGCACCAG	3993
rs773911163	snp	C/T	1.6636e-05	0.00288405	intron-variant	LLGL2	GRCh38.p7	17:75569205	GGCTGCTCACAGGGC[C/T]CCTCCCCTTCTCCAG	3993
rs773927016	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75553011	CTGGGAGACGGCTCC[A/G]GCTGCTGACTTCCTG	3993
rs773943255	snp	A/G	0.000372093	0.0136348	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558513	TGTGCCCTCGCCAGT[A/G]CCAGCTGGTCACCCT	3993
rs773955112	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75530971	GGCCAAGAGTGAGAG[A/C]CGGTTGCCTGGGAGT	3993
rs773994090	snp	A/C	3.36163e-05	0.00409963	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573147	GGGAGCACCACCTGG[A/C]AGTCCTTACCAACCT	3993
rs774009412	snp	C/T	1.6625e-05	0.00288309	intron-variant	LLGL2	GRCh38.p7	17:75569214	CAGGGCCCCTCCCCT[C/T]CTCCAGGTGGGCTCC	3993
rs774030720	snp	C/T	1.68173e-05	0.00289972	intron-variant	LLGL2	GRCh38.p7	17:75558271	ACAGGAAGCCACTTC[C/T]ATGCCCTCCTTGCCT	3993
rs774060132	snp	A/G	1.78121e-05	0.00298425	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570950	GCCCACCCCTTGCAG[A/G]CACAGGAGGGGAGTG	3993
rs774063094	snp	C/T			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524240	TATGGCTGGGTCTCA[C/T]TCTAACCCTTTGTCC	3993
rs774064085	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75570776	TGCTGGGGGCCCAGG[C/T]AGGCTCCCCCAAGGG	3993
rs774076832	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542856	GGAGAGGCTGAGGCC[A/G]AGAGTCCCTGGACAG	3993
rs774116055	snp	C/T	1.67203e-05	0.00289134	intron-variant	LLGL2	GRCh38.p7	17:75568707	TGGTAGGTCTGGCCC[C/T]GGCCCCAGCCCCAGC	3993
rs774119689	snp	C/T	3.38003e-05	0.00411084	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563411	CTACTGCCAGTGGCC[C/T]GTGTCCAGCGAAGCC	3993
rs774122799	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75531239	CCTCCCTTTGGAAGA[C/T]GAAGTGCTGCCTGGG	3993
rs774123481	in-del	-/TT			intron-variant	LLGL2	GRCh38.p7	17:75530988	GGTTGCCTGGGAGTC[-/TT]TCCTGTGGTGGGGAT	3993
rs774136253	snp	C/G	1.66106e-05	0.00288184	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556108	CCCGTCCCTGCGCAT[C/G]CTGGCCATCGGCACC	3993
rs774237495	in-del	-/TT			intron-variant	LLGL2	GRCh38.p7	17:75532078	CACACACACACACAC[-/TT]TTTTTTTTTTTTTTT	3993
rs774248063	snp	C/T	1.6949e-05	0.00291105	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573498	TTCTACCTGATCTCA[C/T]CCTCGGAGTTTGAGC	3993
rs774279278	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542876	TCCCTGGACAGCCTT[C/G]CCCGAGGTCAGAAGG	3993
rs774287105	snp	A/G	8.47925e-05	0.00651069	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571778	AGCCTGTGCGGGCAG[A/G]GCAGGGTGAGTGCTG	3993
rs774294121	snp	A/G	0.000113424	0.00752987	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574409	GGGCTGTGGCTAGCC[A/G]CCCCAAGGGCCTCAG	3993
rs774392679	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75569333	CAGGGCAGGTAGCAG[G/T]CTGGGCTGGGGAGGG	3993
rs774400240	snp	G/T	1.65567e-05	0.00287716	intron-variant	LLGL2	GRCh38.p7	17:75563705	GTGGGGACTGACACT[G/T]GTCTGAGAGTTTGAG	3993
rs774411747	snp	C/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523245	AATGTGACTCCCCTC[C/T]CCAGTACCTTGTTTT	3993
rs774412733	snp	C/T	6.24135e-05	0.00558595	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570361	AGGTGCACACTGCAC[C/T]CCAGTGACCAGCTGG	3993
rs774446762	snp	C/T	3.37935e-05	0.00411043	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570160	GGCTGTGGTCACCTC[C/T]TTGGCCCTGCACTCT	3993
rs774467399	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75528613	CATGGTGGCACATGC[C/G]TGTAATCCCAGCTAC	3993
rs774500920	snp	C/G	3.15642e-05	0.00397254	intron-variant	LLGL2	GRCh38.p7	17:75557992	GGCCAGGGCTGCTGT[C/G]TCTCCTCCCCACCCT	3993
rs774503393	snp	A/G	0.000234781	0.0108321	intron-variant	LLGL2	GRCh38.p7	17:75558075	TTTGCATCATTGCAC[A/G]TGGGCCCCGAGGGCC	3993
rs774520764	snp	C/T	1.76849e-05	0.00297357	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569033	GTCTGCCTGCGGCTG[C/T]TCTACAAACTCAGCA	3993
rs774552496	snp	A/G	3.33533e-05	0.00408357	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569293	CTCTGCAAGTACAGC[A/G]GCTACCTGGCTGTGG	3993
rs774558189	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567616	TACACTCCAGCCTGG[A/G]TGACAGAGCAAGACT	3993
rs774559439	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75554881	CGACAGCGCAAGACT[-/C]CCGTCTCAAAAAAAA	3993
rs774564854	in-del	-/AAACAAAC			intron-variant	LLGL2	GRCh38.p7	17:75528743	ACTCCATCTCAAAAC[-/AAACAAAC]AAACAAACAAACAAA	3993
rs774569798	snp	A/G	3.33673e-05	0.00408442	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570446	CATTCCGCCGGATGC[A/G]TCGGAGCCGGGTGTC	3993
rs774571964	snp	C/T	0.000112822	0.00750989	intron-variant	LLGL2	GRCh38.p7	17:75568951	CTGGCATCCCTCTCA[C/T]GCCTGGCAGGTGGGT	3993
rs774588074	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539979	CACTGCTGTATCCCT[C/T]TCCTAGGACAGTGTC	3993
rs774590278	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75527981	TTTTTTAGAAAGGGG[C/G]TTTTGCCATGTTGCC	3993
rs774595188	in-del	-/AG			intron-variant	LLGL2	GRCh38.p7	17:75539082	TGTTTGTTTTGAGAC[-/AG]AGTTTCGCTCTGTCA	3993
rs774595912	snp	C/T	1.6782e-05	0.00289668	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563080	CTGCAGGAGCACCCT[C/T]GAGACCCCAACCAGA	3993
rs774596668	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566074	TATTTGCGCAGACAC[G/T]GAAGCAGTCTGATGG	3993
rs774628973	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75557945	ACTGGGAAAAATCTC[C/T]CAGGGATCAGGTCAC	3993
rs774640862	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555942	AACCGGAAAGGTACC[A/G]AAGCCCTGCTTCCTG	3993
rs774711760	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75531659	GACAGGGCAGGAGAC[A/G]GGCGTCCCCCAGCGG	3993
rs774719620	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75554866	TGCACTCCAGCCTGG[-/G]CGACAGCGCAAGACT	3993
rs774742501	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75548525	AAAGAAGTGGCCGGG[C/T]GCCGTGTCTCCTGCC	3993
rs774777522	in-del	-/CTG	1.72646e-05	0.00293803	cds-indel, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570026	CAGGTGGAGGCCGAC[-/CTG]CTGCAGGACCAAGAG	3993
rs774800638	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572122	ACATCCAGGAGGCTC[A/G]GACCTTGGGCAAAAA	3993
rs774843603	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75571894	ACCCACCTCCTCCCC[C/T]TAGCCAAGGAGATCC	3993
rs774856704	in-del	-/AAA			intron-variant	LLGL2	GRCh38.p7	17:75548757	TGAGATTCTGTCTCA[-/AAA]AAAAAAAAAAAGCCA	3993
rs774877468	snp	A/G	6.88855e-05	0.00586839	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558566	CTTTGGAGCCTGAAG[A/G]TCAAGGGCGGGGCAT	3993
rs774885657	in-del	-/TCA			intron-variant	LLGL2	GRCh38.p7	17:75530648	GAGCGAGACTCCATT[-/TCA]AAAAAAAAAAAAAAA	3993
rs774932901	snp	A/G	3.37314e-05	0.00410665	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568507	TGCCCTGGTGGTGCT[A/G]GCTGAGGAGGAGCTG	3993
rs774933314	snp	C/T	1.73806e-05	0.00294788	intron-variant	LLGL2	GRCh38.p7	17:75563009	TCACGGCACTCCCCT[C/T]GCCCAGGTTGCCAGA	3993
rs774952733	snp	A/C	3.05535e-05	0.00390843	intron-variant	LLGL2	GRCh38.p7	17:75573658	GGCCAGAGGCCTCTC[A/C]CGCCCCTCCCGCCCC	3993
rs774998034	snp	A/G			intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523544	GGTTCAGAGCCCCCA[A/G]CCCTCAAGTGGCACC	3993
rs775057584	snp	A/G	8.90036e-05	0.00667037	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564567	GCATGGGGCAGGACC[A/G]TCAGTAAAGACAGGG	3993
rs775058370	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75563295	GCCGCCTCGGTCCAG[C/T]GTGCTGCCCTCTGTC	3993
rs775131422	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75547131	CAACTCCTTTATACC[C/T]ACACCAAGCCCGATG	3993
rs775161804	snp	A/G	1.70414e-05	0.00291898	intron-variant	LLGL2	GRCh38.p7	17:75563486	TTTCACCCGCCGGGC[A/G]GGGCCCACCCCCAGT	3993
rs775169385	snp	A/C	2.02419e-05	0.00318128	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568436	AGAGCTGGGCTGCTT[A/C]CTCCTGGCCCCGGCC	3993
rs775189675	snp	C/T	1.66902e-05	0.00288874	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543495	GGACCTGTTCCAGTT[C/T]AACAAGGTAAGTTAG	3993
rs775222763	snp	A/G	1.6886e-05	0.00290564	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563414	CTGCCAGTGGCCCGT[A/G]TCCAGCGAAGCCCAG	3993
rs775224400	snp	A/G	1.70246e-05	0.00291754	intron-variant	LLGL2	GRCh38.p7	17:75569329	ACGGCAGGGCAGGTA[A/G]CAGGCTGGGCTGGGG	3993
rs775228536	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75551774	TATGAGCCATGTATG[C/T]GATTTAAAATTTCCT	3993
rs775241476	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529487	TGGGATTACAGGCAT[A/G]AGCCACTGCACCCGG	3993
rs775261195	snp	A/G	1.64833e-05	0.00287078	synonymous-codon, missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523666	TTGTATTGTCAGGCT[A/G]TTGGAGAAGTCTGGG	3993
rs775281916	snp	C/T	4.05638e-05	0.00450336	intron-variant	LLGL2	GRCh38.p7	17:75558637	CCCAGGGTAAGGGCT[C/T]AATCCCCAGCCCCTT	3993
rs775294112	snp	C/G	4.14293e-05	0.00455115	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574575	TGAGAGTGGAGGTCC[C/G]TGAGGCCATGACTCC	3993
rs775322395	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75574732	TGGGAGGAAGAGCCC[C/T]GGCCCCACTCCCCTG	3993
rs775324679	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75562756	TATATTTTTAGTAGA[A/G]ACAGGGTTTTGCCAT	3993
rs775393330	snp	C/T	1.67894e-05	0.00289731	intron-variant	LLGL2	GRCh38.p7	17:75568717	GGCCCTGGCCCCAGC[C/T]CCAGCCCCACCGCAA	3993
rs775405088	snp	A/C	1.69844e-05	0.00291409	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570491	ACCCGGCTGGCCCCC[A/C]AGGAGAGGTGAGGCC	3993
rs775434892	snp	A/G	1.68898e-05	0.00290596	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573108	GCGTGGCCCACTTCG[A/G]CAGTCGTCGAGCCGA	3993
rs775448054	in-del	-/T	7.95846e-05	0.00630761	intron-variant	LLGL2	GRCh38.p7	17:75573678	CCTCCCGCCCCTCCC[-/T]GCCCTCTCTGAGATA	3993
rs775510188	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75556576	TGCAGGGGTTGTATT[C/G]GTGGATCCAGAGGGA	3993
rs775518531	snp	A/G	1.76421e-05	0.00296998	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569051	TACAAACTCAGCACT[A/G]TGCGCGTGTTCCTCA	3993
rs775588618	in-del	-/GAGGTGAGGCCT	7.24874e-05	0.00601984	intron-variant, cds-indel	LLGL2	GRCh38.p7	17:75570496	GCTGGCCCCCCAGGA[-/GAGGTGAGGCCT]GAGGTGAGGCTGCGG	3993
rs775594497	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75538768	GGGGAGGGCGTGAAG[A/G]TATCTGGAGGAAAGT	3993
rs775599771	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75545408	CACTTTTACAGTCTG[C/T]AGGAGGGAGGAGGCT	3993
rs775603732	snp	A/G	1.86451e-05	0.00305323	intron-variant	LLGL2	GRCh38.p7	17:75573314	GGGTGTCGGGGCCCC[A/G]GGCACTGCACGGACG	3993
rs775624603	snp	C/T	1.79075e-05	0.00299223	stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568817	ACCCCAGCCCCACCC[C/T]AGAGGGACCTGCTGC	3993
rs775632315	snp	C/G	1.64751e-05	0.00287007	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524298	CCTCTGCAGCCTCAA[C/G]CGGTTGTCTTACCAG	3993
rs775693592	snp	A/C	1.67871e-05	0.00289711	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568529	GAGGAGCTGGTGGTG[A/C]TTGACCTGCAGACAG	3993
rs775726524	in-del	-/CAAAAAAA			intron-variant	LLGL2	GRCh38.p7	17:75554302	AGCAAAACTCCGTCT[-/CAAAAAAA]AAAAAAAAAAAGCCA	3993
rs775747643	snp	C/T	3.3071e-05	0.00406625	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563798	CCTCTGGCTGACCAC[C/T]AGGCAGGGGTAGGTA	3993
rs775749543	snp	C/T	1.70755e-05	0.00292189	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569104	CTTCAGTGCCCAGGG[C/T]GAGGACGAGTGGCCC	3993
rs775773584	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566041	AAGGGTTGGCAAGGC[C/T]TCCCTGATAAGGGGA	3993
rs775815682	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75555240	GAAGGATGTACACTT[A/C]GGTTCTAGCAAGGTT	3993
rs775989945	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75529667	GGAGATCGAGACCAT[C/G]CTGGCCAAGATGGTG	3993
rs775993202	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75559673	TAATGTCACCGACTG[G/T]CAGTCCAGTGTCCTT	3993
rs776018169	snp	A/G	3.65143e-05	0.00427268	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570457	ATGCGTCGGAGCCGG[A/G]TGTCCAGCCGGAAGC	3993
rs776037179	in-del	-/AAA/AAAA			intron-variant	LLGL2	GRCh38.p7	17:75572664	GCGAGATTCCGTCTC[-/AAA/AAAA]AAAAAAAAAAAAAAA	3993
rs776066508	snp	C/T			intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523454	GGACTCCTACCCCTA[C/T]GCCTAGCTCTGAGCA	3993
rs776072926	snp	A/G	1.80266e-05	0.00300216	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572063	CAGAGGAGCAGTTCA[A/G]GGTGCCACACGGGCA	3993
rs776084658	snp	A/G	1.8744e-05	0.00306131	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569963	TGCCACCCTGCGCAG[A/G]TGCTGGTACTGGAAC	3993
rs776092410	snp	A/G	5.00446e-05	0.00500198	intron-variant	LLGL2	GRCh38.p7	17:75558084	TTGCACATGGGCCCC[A/G]AGGGCCTGGCACTCA	3993
rs776196086	snp	A/T	1.66355e-05	0.002884	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568625	CACCACGTCTCCAAC[A/T]TCCCGCTGAAGCTGT	3993
rs776205394	snp	C/G	1.67576e-05	0.00289457	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563097	AGACCCCAACCAGAT[C/G]CTGATCGGCTACAGC	3993
rs776207881	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530616	GATCGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC	3993
rs776277690	snp	C/T	3.36479e-05	0.00410157	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563109	GATCCTGATCGGCTA[C/T]AGCCGAGGCCTCGTT	3993
rs776291134	snp	A/C	2.20262e-05	0.00331853	intron-variant	LLGL2	GRCh38.p7	17:75559237	TCGGCTCACGGGCAG[A/C]TGTTCTTGTCACAGG	3993
rs776327762	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544401	AAGGAAGCAGTGGAT[A/G]TGAGACCAGACAGTC	3993
rs776343821	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75550706	GGATCACTTGAGCCC[A/G]GGAGGAGGAGGTTAC	3993
rs776411930	snp	C/G	1.65075e-05	0.00287289	upstream-variant-2KB, stop-gained, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523708	CATCTTTGATGTTTA[C/G]CAGGCCGACGCTGTG	3993
rs776459233	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75555695	CTCCCCCTACTTTCC[C/G]CACCCCACACCCATA	3993
rs776462302	snp	A/G	1.9062e-05	0.00308717	intron-variant	LLGL2	GRCh38.p7	17:75568941	GGCATCCCGGCTGGC[A/G]TCCCTCTCACGCCTG	3993
rs776476913	snp	C/G	1.68442e-05	0.00290204	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573196	CTCGCTGCCCCTGCT[C/G]AAGCCCCAGGTGCGC	3993
rs776546878	snp	C/T	3.32729e-05	0.00407864	intron-variant	LLGL2	GRCh38.p7	17:75569187	GCTGGGTCCTGTCCC[C/T]GTGGCTGCTCACAGG	3993
rs776561571	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75554154	TGAAAATACAAAAAT[C/T]AGCTGGGCATGGTGG	3993
rs776595225	in-del	-/TCCC	0.000145811	0.00853721	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574571	CGCTGAGAGTGGAGG[-/TCCC]TCCCTGAGGCCATGA	3993
rs776603642	snp	A/G	1.73168e-05	0.00294246	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523768	ACCCTATGCCCGGAT[A/G]TGCATTAGTGGGTAC	3993
rs776633119	snp	A/G	6.69826e-05	0.00578678	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571061	TCCTTCACAGGCTTC[A/G]TCCGGACCCTGTACT	3993
rs776647855	snp	C/T	3.3054e-05	0.00406521	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563782	AAGCGATTACCAGAA[C/T]CCTCTGGCTGACCAC	3993
rs776664467	snp	C/T	1.67419e-05	0.00289321	intron-variant	LLGL2	GRCh38.p7	17:75558650	CTCAATCCCCAGCCC[C/T]TTCCACTCCCAGCCC	3993
rs776786578	in-del	-/GT			intron-variant	LLGL2	GRCh38.p7	17:75555423	CCCAGGTTTTTCACA[-/GT]GTGTGTGTGTGTATT	3993
rs776847298	snp	A/T	1.71666e-05	0.00292968	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573577	ATTCAGCAGAAACCA[A/T]GAACCACCGCCCTGG	3993
rs776860943	snp	C/T	3.53719e-05	0.00420532	intron-variant	LLGL2	GRCh38.p7	17:75571878	CCTCACCAGCCCCAA[C/T]ACCCACCTCCTCCCC	3993
rs776878589	snp	A/G	3.36927e-05	0.00410429	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563171	TCTACCACTTCCTCA[A/G]CAGCCAGGTAGGCAG	3993
rs776880112	snp	A/G	4.99871e-05	0.0049991	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559354	GTTTGTGGTGCAGCT[A/G]CCAGCTTTTCGTGCG	3993
rs776942164	snp	C/T	3.48851e-05	0.00417628	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570175	CTTGGCCCTGCACTC[C/T]GAGTGGCGGCTCGTG	3993
rs777072495	in-del	-/TC	3.50318e-05	0.00418505	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524548	CCTTGGCCCTGGGTG[-/TC]TCTGATACTCACAGA	3993
rs777074577	snp	G/T	1.65127e-05	0.00287334	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558169	GCTACGGAGCCCCAG[G/T]CGTGGAGTTCATGGG	3993
rs777128389	snp	G/T	1.68015e-05	0.00289836	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570464	GGAGCCGGGTGTCCA[G/T]CCGGAAGCGGCACCC	3993
rs777141808	snp	A/G	1.65916e-05	0.00288019	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574952	GTCCCTGCCCCAACC[A/G]GAGAGGCCGGTGCAC	3993
rs777218187	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75540221	GTTCATACCAGGCGT[C/T]TCTAGGCCTGGCTTC	3993
rs777227966	snp	C/T	1.73309e-05	0.00294366	intron-variant	LLGL2	GRCh38.p7	17:75568763	GGACTTCTTGGTCTC[C/T]TTTTCTAGGAGTGGC	3993
rs777230922	snp	A/G	3.45214e-05	0.00415446	intron-variant	LLGL2	GRCh38.p7	17:75563288	TGGGAACGCCGCCTC[A/G]GTCCAGCGTGCTGCC	3993
rs777253337	in-del	-/CTT			intron-variant	LLGL2	GRCh38.p7	17:75540018	GCCAAGCTCTTGCTC[-/CTT]CTACAGGATCTGTGT	3993
rs777287526	snp	A/C/T	8.03826e-05	0.00633915	intron-variant, missense	LLGL2	GRCh38.p7	17:75570505	CCAGGAGAGGTGAGG[A/C/T]CTGAGGTGAGGCTGC	3993
rs777306225	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541818	CACTGCAACCTCCGC[C/G]TCTTGGGTTCTAGCA	3993
rs777325953	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75556357	ATCCCTGGTGGGATG[C/T]GACCCTGTCCTTTGC	3993
rs777341295	snp	A/T	8.46518e-05	0.00650528	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559385	CTGGAGGACCGGACC[A/T]TCAGCTCGGACGCGG	3993
rs777348620	snp	A/C	1.80569e-05	0.00300468	intron-variant	LLGL2	GRCh38.p7	17:75559459	CCCCTCAAGTTAGGC[A/C]TGGCTTCTCCCCTTG	3993
rs777349829	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75557034	CTCTGTCTCAAAAAC[-/T]TTTTTTTTTTTTTTT	3993
rs777352514	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75537877	ACAGTGGCACAATCT[C/T]GATTCACTGCAGCCT	3993
rs777374981	snp	A/G	1.64765e-05	0.00287019	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524380	TTCTACAGCTTCAGG[A/G]ACTTCACGTTGCCCC	3993
rs777388568	snp	A/G	1.78242e-05	0.00298526	intron-variant	LLGL2	GRCh38.p7	17:75571851	CAGGGAGTGGCTCCA[A/G]CCCTGCCACCCCCTC	3993
rs777402364	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544035	GGGAGAGGTGCCCAG[A/G]AGAATGAGCCGGAGT	3993
rs777421701	snp	C/T	2.44597e-05	0.00349704	intron-variant	LLGL2	GRCh38.p7	17:75570307	GGGCCCGCGAGGACT[C/T]CCAGGACCTAGCAGC	3993
rs777523567	snp	C/T	0.000145127	0.0085172	intron-variant	LLGL2	GRCh38.p7	17:75570542	CCACGCACCCAGGTT[C/T]GGCTCAGAGCAGCCA	3993
rs777572872	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75538627	CTGCTGCTTGTGGGG[C/G]ATTCCACAGGTAATC	3993
rs777589961	in-del	-/TG	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523262	CAGTACCTTGTTTTC[-/TG]TGTCCTTGTAGCCGT	3993
rs777624951	snp	C/T	1.66613e-05	0.00288623	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556100	GGCTACAGCCCGTCC[C/T]TGCGCATCCTGGCCA	3993
rs777640299	snp	A/C	1.80335e-05	0.00300273	intron-variant	LLGL2	GRCh38.p7	17:75564335	CCCAGCCCACTGCCG[A/C]TCCTCTGTGCCTGCC	3993
rs777663029	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543151	TAAATGGCTTCCTCC[C/T]CCAGCTTTTCCTACC	3993
rs777687815	snp	C/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566403	CCTCAGCTTGGGCTG[C/T]GGTGCAGGCCATGGG	3993
rs777708347	snp	C/T	3.32856e-05	0.00407942	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564449	CCAGCAGACGGCCTT[C/T]GACTTCACCTCCCGT	3993
rs777756217	snp	C/T	1.68593e-05	0.00290334	intron-variant	LLGL2	GRCh38.p7	17:75569153	CCAGGAGCCTGGGAC[C/T]CAGGAAGGGCAGAGG	3993
rs777761604	snp	C/T	1.69833e-05	0.00291399	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524481	TCTCAGGGACCATCT[C/T]GGCTGCCTCCTGTAC	3993
rs777802930	snp	A/G	6.82629e-05	0.00584181	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573544	CCAAGTGGCTGGTGG[A/G]GCCCCGGTGTCTGGT	3993
rs777828760	in-del	-/TTT/TTTT			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541720	GTGGCTCTGCTTTTT[-/TTT/TTTT]TTTTTTTTTTTTTTT	3993
rs777834005	snp	C/T			upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524780	CTCTCGCCCCCGTCC[C/T]GTTGTCAGTGGAACT	3993
rs777851165	snp	G/T	3.57111e-05	0.00422543	intron-variant	LLGL2	GRCh38.p7	17:75543551	GTTTTCGGCCAAGCA[G/T]CTCAGGCTGGGGCTG	3993
rs777856235	snp	A/T	5.0942e-05	0.00504662	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573487	ACTCCCCAGGCTTCT[A/T]CCTGATCTCACCCTC	3993
rs777857719	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530365	AAAAAATTAGCTGGG[C/T]ATCAGCCAGGCGCGG	3993
rs777932452	snp	A/C	3.42021e-05	0.0041352	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572010	TGATCTGTCGAAGAG[A/C]CCTGACATGCAGGGA	3993
rs777959624	snp	A/G			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524033	CCCAGCAGAAGGGAT[A/G]TGGATTGTGGGGATT	3993
rs777972948	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75561620	AATGAGATCCTGTCT[C/G]TAAAAAGATTAAAAA	3993
rs777978604	snp	C/T	3.46855e-05	0.00416432	intron-variant	LLGL2	GRCh38.p7	17:75569375	GGAGTGGTCGATGAC[C/T]GGGGACAGCAGGGAC	3993
rs777985781	snp	C/T	4.26576e-05	0.00461811	intron-variant	LLGL2	GRCh38.p7	17:75573680	TCCCGCCCCTCCCTG[C/T]CCTCTCTGAGATACC	3993
rs778002857	in-del	-/C	1.70084e-05	0.00291615	frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569116	GGCGAGGACGAGTGG[-/C]CCCCCACTCCGCAAG	3993
rs778103561	snp	G/T	1.76512e-05	0.00297074	intron-variant	LLGL2	GRCh38.p7	17:75571125	CAGCCTGGGGTTGGG[G/T]GGCAGGGGGTAGTGG	3993
rs778122987	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75552601	AATTTGTGAAATCTA[A/G]GTGTATTTTACACTT	3993
rs778162753	snp	A/G			utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575142	TTTGTAGTGGGCTGG[A/G]TTTTAAGTTATAAAT	3993
rs778195627	snp	A/G	0.000269116	0.0115968	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573133	AGCCGAGGACTACGG[A/G]GAGCACCACCTGGCA	3993
rs778218563	snp	A/G	3.31961e-05	0.00407394	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523734	CTGTGGCCACATTCC[A/G]AAAGAATAACCCTGG	3993
rs778231917	snp	A/G	4.16528e-05	0.0045634	intron-variant	LLGL2	GRCh38.p7	17:75558022	TAGGCTCCATGCATG[A/G]GTCCTGCTGCCTCGG	3993
rs778245813	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75534540	GGCTGGAGCACAGTG[A/G]TGCCATCATAGCTCA	3993
rs778262331	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75535706	AGGCAAGTCCACCCC[C/G]TGTGGTTATTCTCTC	3993
rs778269487	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75529258	ATGGAGCACAGTGGC[A/G]TGATCTCAGCTCACT	3993
rs778273422	snp	A/G	7.66959e-05	0.0061921	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574522	CCCAGGCCAGCTGGG[A/G]TGGGCCCGAGGCTCT	3993
rs778294856	snp	C/T	6.78725e-05	0.00582509	intron-variant	LLGL2	GRCh38.p7	17:75563473	CTTACGGTCAGTGTT[C/T]CACCCGCCGGGCAGG	3993
rs778306836	snp	C/T	1.64825e-05	0.00287071	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523642	GAGTTCATGTCATAA[C/T]GTTTCTCATTGTATT	3993
rs778318974	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75563978	TTCACGTCTCTCAGC[A/G]GCCCAATTCCTGCCA	3993
rs778368571	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75537992	TTTTTTGTCTTTTTA[G/T]TAGAGATGAGGTTTT	3993
rs778397021	snp	C/T	1.70711e-05	0.00292152	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563038	GAGGAGGCCCGCCAC[C/T]GGCGTGTGTTCGAGA	3993
rs778398192	in-del	-/GGTAAC	1.73208e-05	0.00294281	cds-indel, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573591	AAGAACCACCGCCCT[-/GGTAAC]GGTGCGGGCCCCAAG	3993
rs778403077	in-del	-/GGACCGGGACTGTCTGTTCTC	1.65303e-05	0.00287487	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524448	GGAGCTTGCTCCGGG[-/GGACCGGGACTGTCTGTTCTC]GGACCGGGACTGTCT	3993
rs778432001	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75554986	CATGAGGTCAGGAGA[C/T]AGAGACACGGTGAAA	3993
rs778437766	snp	A/G	1.67601e-05	0.00289478	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571017	TGGCGCCTGTGCAGC[A/G]CAAGATCGAGGCTCG	3993
rs778495578	snp	A/G	9.73833e-05	0.00697726	intron-variant	LLGL2	GRCh38.p7	17:75568913	AGCCCTGAGGTGGAC[A/G]AGCCAGCCCCTGGGC	3993
rs778513077	snp	C/T	3.29647e-05	0.00405971	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523646	TCATGTCATAACGTT[C/T]CTCATTGTATTGTCA	3993
rs778516875	snp	A/C	1.67005e-05	0.00288963	intron-variant	LLGL2	GRCh38.p7	17:75556167	CGTCCCCTCGCTCCC[A/C]CTCGGGCAGGGCCTT	3993
rs778525410	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528370	TCTGCCCCTCTCAGC[C/T]TCCCAAAGTGCTGGG	3993
rs778537988	snp	A/G	1.80153e-05	0.00300122	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574690	GCTCTGGGCTTGAGT[A/G]CAGCTGCCAACCGTG	3993
rs778538444	snp	C/G			intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526284	CCTGCCATCTGGGCT[C/G]TGTCCCTGCCGGCCC	3993
rs778569645	snp	A/G	0.000193834	0.00984274	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568988	CACAGGCACGAGGAC[A/G]GCACGGTGCGGTTCT	3993
rs778599340	in-del	-/CCGTGTTGGGGTCTTGGACACCAGGGAGGGG	1.64955e-05	0.00287184	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564569	TGGGGCAGGACCATC[lengthTooLong]AGTAAAGACAGGGCC	3993
rs778701779	snp	C/T	4.99264e-05	0.00499607	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564462	TTCGACTTCACCTCC[C/T]GTGTCATCGGCTTCA	3993
rs778723478	snp	C/T					GRCh38.p7	17:75527460	TTTGGCATCCCCATT[C/T]TTCCTTGAGGCAAGG	3993
rs778821181	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75549286	GAGGAAGTGCTGCTG[A/G]AGAAGTCAAGGTAAA	3993
rs778876827	snp	C/G	1.79168e-05	0.00299301	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524497	GGCTGCCTCCTGTAC[C/G]CAGACTCTAACCTGT	3993
rs778894877	snp	C/G	1.77991e-05	0.00298316	intron-variant	LLGL2	GRCh38.p7	17:75562975	GGGGCCATTCCCCCT[C/G]GTGGACGGCATCGGA	3993
rs778903743	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75536655	TTTGATCCTCTTATC[C/T]ACCCTGCCTAGGAGG	3993
rs778945450	snp	C/G/T			intron-variant	LLGL2	GRCh38.p7	17:75550228	TCCTGAGTGCAGCCG[C/G/T]GATTCAGGGTTGCTG	3993
rs778958644	snp	C/T	3.42044e-05	0.00413534	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571928	TGATGCACCGGGCGC[C/T]GGTGGTGGGCATCCT	3993
rs778987794	snp	G/T	5.0491e-05	0.00502424	intron-variant	LLGL2	GRCh38.p7	17:75556035	CCCACCCCACGTGCT[G/T]CTCGTTGCAGACGGT	3993
rs779011688	snp	C/T	3.56259e-05	0.00422039	intron-variant	LLGL2	GRCh38.p7	17:75571860	GCTCCAGCCCTGCCA[C/T]CCCCTCACCAGCCCC	3993
rs779014369	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75541302	GACTTCTGACCCAGT[G/T]ACCTTGGCCTGGGCC	3993
rs779071525	snp	G/T	6.48698e-05	0.00569479	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570485	AGCGGCACCCGGCTG[G/T]CCCCCCAGGAGAGGT	3993
rs779157153	snp	C/T	3.33372e-05	0.00408258	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568594	TTCTCTGCACTGTTC[C/T]GCCATCACCTGCTCT	3993
rs779173671	snp	C/T	1.65203e-05	0.002874	intron-variant	LLGL2	GRCh38.p7	17:75558146	GAGCTTTCCTGAGCC[C/T]ACTCCTAGCTACGGA	3993
rs779215019	snp	A/G	1.79242e-05	0.00299362	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573278	ACCAAATATGGCCAA[A/G]GTGTTTGAGCCGGGC	3993
rs779254128	snp	C/T	3.36344e-05	0.00410074	splice-donor-variant	LLGL2	GRCh38.p7	17:75558629	CGTGGACCCCCAGGG[C/T]AAGGGCTCAATCCCC	3993
rs779263343	snp	C/T	6.90715e-05	0.00587631	intron-variant	LLGL2	GRCh38.p7	17:75563281	CAGGCGATGGGAACG[C/T]CGCCTCGGTCCAGCG	3993
rs779308607	snp	G/T	7.18262e-05	0.00599232	intron-variant	LLGL2	GRCh38.p7	17:75571133	GGTTGGGGGGCAGGG[G/T]GTAGTGGGCAGCAGA	3993
rs779364124	snp	C/T	1.65299e-05	0.00287483	intron-variant	LLGL2	GRCh38.p7	17:75563745	AAGCCGATTCCTTTC[C/T]TTTCAGGTCCCTTTC	3993
rs779370953	snp	C/G	1.64779e-05	0.00287031	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524224	GAGCTTAGGAGTGGG[C/G]TATGGCTGGGTCTCA	3993
rs779397994	in-del	-/GCCTCTCCC	8.92021e-05	0.00667781	intron-variant	LLGL2	GRCh38.p7	17:75573651	GTGAAAGGGCCAGAG[-/GCCTCTCCC]GCCCCTCCCGCCCCT	3993
rs779463714	in-del	-/GAGCCGGGCTGGGTGGGTGTCGGG	1.81454e-05	0.00301203	intron-variant	LLGL2	GRCh38.p7	17:75573284	ATGGCCAAGGTGTTT[-/GAGCCGGGCTGGGTGGGTGTCGGG]GAGCCGGGCTGGGTG	3993
rs779539721	snp	A/G	1.70371e-05	0.0029186	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573234	GCATCCGCCGGGAGG[A/G]CGTCAGTGGCATCGC	3993
rs779571504	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75538338	CTCTCTCATGTCATC[G/T]GCACAGATCTCTGCA	3993
rs779578250	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75536539	GGTTGCGGTGGCTGG[A/T]GAGGAGCCCACGCCT	3993
rs779595790	in-del	-/CTT	1.71659e-05	0.00292962	intron-variant	LLGL2	GRCh38.p7	17:75568751	AAACTCTCCCATGGA[-/CTT]CTTGGTCTCTTTTTC	3993
rs779615590	snp	C/T			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575434	ACCATCTTGAGTCTG[C/T]CTGACTTTTTCCCTG	3993
rs779639879	snp	C/T	1.69525e-05	0.00291135	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571701	GCTGTGGGCTGGCAC[C/T]AATGGGGGCACCATC	3993
rs779644096	snp	C/T	1.71009e-05	0.00292406	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523763	GGCAAACCCTATGCC[C/T]GGATGTGCATTAGTG	3993
rs779680658	snp	A/G	0.000118968	0.00771166	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571947	GGTGGGCATCCTGGT[A/G]CTCGACGGACACAGC	3993
rs779703795	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75564116	GGTGATGTTCAAACA[A/G]AATTGGTGGGGGCAC	3993
rs779741960	snp	C/T	1.77021e-05	0.00297502	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568470	GACCCTTGCCCTGTA[C/T]CCCAGCCTTTGACGA	3993
rs779793958	snp	G/T	4.2076e-05	0.00458653	intron-variant	LLGL2	GRCh38.p7	17:75573678	CCTCCCGCCCCTCCC[G/T]GCCCTCTCTGAGATA	3993
rs779835258	snp	A/G	1.6571e-05	0.0028784	intron-variant	LLGL2	GRCh38.p7	17:75563840	CCTCTTTCCTCTCCA[A/G]AGCCTTCCTGGAGGG	3993
rs779940942	snp	C/T	1.87057e-05	0.00305819	intron-variant	LLGL2	GRCh38.p7	17:75558033	CATGGGTCCTGCTGC[C/T]TCGGGGGAGGGCAGC	3993
rs779967269	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75529617	CCTGTAATCCCAGCA[C/G]TTTGGGAGACCGAGG	3993
rs779978869	in-del	-/AG			intron-variant	LLGL2	GRCh38.p7	17:75536087	AGAGCAGGGCAGAAC[-/AG]GGAGGGTGGCTCAGA	3993
rs779981547	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530286	GGAGGGAGGATTGCT[C/T]GAACCCAGGAGTTCA	3993
rs780012200	snp	A/G	1.69963e-05	0.00291511	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563042	AGGCCCGCCACCGGC[A/G]TGTGTTCGAGATGGT	3993
rs780085281	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75546464	ACGAATCGAAGGCCA[C/T]GTCTGGCTGGCGGCT	3993
rs780147308	snp	A/C/G	3.35319e-05	0.00409451	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573076	GGCCCTGGAGGGCTC[A/C/G]AGAGTGCGGCGGGTC	3993
rs780155197	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75550200	CAGGGGCTATGCCCC[A/G]TCCCGCCCTCTGTCC	3993
rs780162660	snp	C/G/T			intron-variant	LLGL2	GRCh38.p7	17:75557646	GCACTCGAGTTCCAG[C/G/T]CTGGGCTGGTGTACA	3993
rs780266104	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75572218	GTGAGGGGGGAGTCT[C/T]GTGTGAGGACACTGA	3993
rs780349290	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75571488	TGGTTCTCCCCTGCT[C/G]TATCACAGCAAGGGC	3993
rs780355613	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75562310	CTGAATATGAATGTA[C/T]AGTTTAACAGATTCT	3993
rs780363548	snp	C/T	6.65214e-05	0.00576683	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568667	ATTGCCGCCGGCAGC[C/T]GGCAGAACGCACACT	3993
rs780370026	snp	A/G	1.70179e-05	0.00291696	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563365	GGCAGCGGGACGGCC[A/G]CCTGCTCGTCAGCTG	3993
rs780370741	snp	A/T	1.75829e-05	0.00296498	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570047	CAGGACCAAGAGGGC[A/T]ACCGCTGGAAGGGGC	3993
rs780378430	snp	A/G	7.39276e-05	0.00607934	intron-variant	LLGL2	GRCh38.p7	17:75570908	ACTGTTCCTGGGGAG[A/G]GGAGTCCAGAGCTGA	3993
rs780380010	snp	C/T	1.80912e-05	0.00300754	intron-variant	LLGL2	GRCh38.p7	17:75572988	TGGTTTGGCCATGGG[C/T]ATGAACAACCACCCC	3993
rs780391924	snp	C/T	1.66852e-05	0.0028883	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556087	GCCCAGCGCCCTCGG[C/T]TACAGCCCGTCCCTG	3993
rs780395498	snp	G/T	7.31342e-05	0.00604663	intron-variant	LLGL2	GRCh38.p7	17:75558487	GGTAGCAAGACCACA[G/T]GATCCCGTCGTGTGC	3993
rs780397472	snp	C/T	1.64792e-05	0.00287042	upstream-variant-2KB, missense, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524392	AGGGACTTCACGTTG[C/T]CCCAGGATGTGGGGC	3993
rs780420344	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532816	TCCACAAGGGTATTC[C/T]GAACAGGATGCCAGG	3993
rs780437502	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75535885	TATTTTGCCGGCCAG[A/G]TGCAGACGTGGGTGA	3993
rs780518611	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75535829	CCTGTTCTTTCCAAG[G/T]GGGTGTCCAGGTGTG	3993
rs780537387	snp	C/T	1.71062e-05	0.00292451	intron-variant	LLGL2	GRCh38.p7	17:75573465	CCAGGCCGCTAGCAT[C/T]GCCCCCACTCCCCAG	3993
rs780549229	snp	C/G	0.00021333	0.0103257	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574671	AGCAATGGCGGAGGT[C/G]GGGGCTCTGGGCTTG	3993
rs780580538	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75527244	CAAGGAGAACTGTGC[A/G]AGAGATGTCTCAGCT	3993
rs780597130	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75553940	TCTAGCAACAAAGTA[A/C]ATACTCAACAATAAA	3993
rs780601446	snp	C/T	8.60227e-05	0.00655774	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570121	TGGCTTTCAGCCCTT[C/T]GTGTTGGTGCAGTGT	3993
rs780676875	snp	C/T	8.32244e-05	0.00645022	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568610	GCCATCACCTGCTCT[C/T]ACCACGTCTCCAACA	3993
rs780706584	snp	A/C	0.00212879	0.0325555	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574218	TACCTTCCAGAGAAG[A/C]AGCCCGGCCTGGTGA	3993
rs780710960	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75546201	CAGGCCTTGGGAGGG[G/T]GAGCCCAGGCCAGGA	3993
rs780719806	snp	A/G	1.6922e-05	0.00290873	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571714	ACCAATGGGGGCACC[A/G]TCTATGCCTTCTCCC	3993
rs780825793	snp	C/T			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575316	AGCCCTGGCCTGGGC[C/T]GGTGTCAGGAGAATC	3993
rs780882675	snp	A/G	1.67781e-05	0.00289634	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563125	AGCCGAGGCCTCGTT[A/G]TCATCTGGGACCTAC	3993
rs780883245	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75545308	TTCTTCTTTCCATTC[A/G]TATGCAAGAAGCATG	3993
rs780895821	in-del	-/TTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75557036	TCTGTCTCAAAAACT[-/TTTTTTTTTTTT]TTTTTTTTTTTTGTG	3993
rs781048098	snp	A/G	3.30726e-05	0.00406635	intron-variant	LLGL2	GRCh38.p7	17:75558123	AGGGGATGGTGTCCG[A/G]CCTTCCAGAGCTTTC	3993
rs781075944	snp	C/T	3.29538e-05	0.00405904	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524250	TCTCACTCTAACCCT[C/T]TGTCCCTGCAGATTT	3993
rs781094362	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75551133	CCCTGTCCAGGTAGA[C/G]TCGCTGTGAAGGTCA	3993
rs781102270	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539897	TACAGGTGTGAGTTA[C/T]TGCGGCTGGTTGGAA	3993
rs781112775	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75541199	CTGTGTGGAGTCTTT[A/G]GCACGGATGGCCCTG	3993
rs781136608	snp	C/G	9.13617e-05	0.00675815	intron-variant	LLGL2	GRCh38.p7	17:75573292	AGGTGTTTGAGCCGG[C/G]CTGGGTGGGTGTCGG	3993
rs781172937	snp	C/T	1.66449e-05	0.00288482	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568660	GCGGATCATTGCCGC[C/T]GGCAGCCGGCAGAAC	3993
rs781174936	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75556479	TTTACTCAGTTTCCC[C/G]TCTCACCTATTCCTG	3993
rs781212169	snp	C/T	1.7182e-05	0.00293099	intron-variant	LLGL2	GRCh38.p7	17:75569364	GGAGCTGGGGAGGAG[C/T]GGTCGATGACTGGGG	3993
rs781219218	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528969	CGAGACTAGCCTTGC[C/T]CACACAGTGAAACCG	3993
rs781281059	snp	A/G	1.65201e-05	0.00287398	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574909	GGCTGCGCGATGAGC[A/G]CACACTACTACTGAT	3993
rs781378676	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532624	CGGGGGGGTTTCCAC[C/T]ATGTTGGTCAGGCTG	3993
rs781397188	snp	C/T	8.40357e-05	0.00648157	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571005	AGAACATGGAGCTGG[C/T]GCCTGTGCAGCGCAA	3993
rs781415988	snp	A/G	1.71278e-05	0.00292637	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564543	GGTGCCCAGGGTTAG[A/G]TGTGGGAGGCATGGG	3993
rs781516709	snp	A/G	3.31713e-05	0.00407242	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570207	CCTTCGGCACCAGCC[A/G]TGGCTTTGGCCTCTT	3993
rs781542063	snp	C/G	1.64822e-05	0.00287068	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523627	AAAGGTTGGGGAGAA[C/G]AGTTCATGTCATAAC	3993
rs781542922	snp	C/T	1.65894e-05	0.00288	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569254	TACAGTGATGACCCC[C/T]GGCTGGGCATCCAGA	3993
rs781561461	snp	A/G	1.64741e-05	0.00286998	missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523314	TGCTGCAGACAACAC[A/G]CCTTCCTGATGGAGG	3993
rs781619507	snp	C/T	2.13737e-05	0.003269	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524518	TCTAACCTGTAGCTT[C/T]AGAGGCCAGTCTGGG	3993
rs781619774	snp	C/T	9.04527e-05	0.00672445	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574502	AGACCGCGGGTGAGG[C/T]ACCGCCCAGGCCAGC	3993
rs781628295	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75527138	GGCGCCACCACACTC[C/T]AGCCTGGGGACAGAG	3993
rs781640286	snp	A/C			upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524099	AGCACCTCCCCAACC[A/C]GTGCTCTGGGGCGCT	3993
rs781684284	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75564016	TCTTGCTCCTTTCTT[C/G]CACCTTCCCAGAGAG	3993
rs781749933	snp	G/T	1.83209e-05	0.00302657	intron-variant	LLGL2	GRCh38.p7	17:75570927	GTCCAGAGCTGACCC[G/T]TAGGCTGGCCCACCC	3993
rs781767443	snp	C/G	1.67961e-05	0.00289789	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573078	CCCTGGAGGGCTCAA[C/G]AGTGCGGCGGGTCAG	3993
rs796299012	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75558859	CCACCTCCTCCATCC[A/G]CACCCCGCCTCCTCC	3993
rs796325519	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75554302	GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs796448688	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75555137	AGCCGAGATCGCACC[A/G]CTGCACTCCAGCCTG	3993
rs796643257	snp	A/G			missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569102	AACTTCAGTGCCCAG[A/G]GCGAGGACGAGTGGC	3993
rs796746055	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75555291	GGGTAATTTTTGTTC[-/T]TTTTTTTTTTTTTTT	3993
rs796770511	in-del	A/TTTTG			intron-variant	LLGL2	GRCh38.p7	17:75548292	CCTTTTTTTTTTTTT[A/TTTTG]ACGGAGTTTAGCTCT	3993
rs796806696	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75558745	CAGTGACTGGCATGC[A/G]TTTGGCCCGATGCAT	3993
rs796832809	in-del	-/AAA			intron-variant, cds-indel	LLGL2	GRCh38.p7	17:75567951	CTGTCTCGAGAAAAG[-/AAA]AAAAAAAAAAAAGAC	3993
rs796947575	in-del	-/AAA			intron-variant	LLGL2	GRCh38.p7	17:75548768	CTCAAAAAAAAAAAA[-/AAA]GCCAAAGAAGTATAC	3993
rs796963980	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75539101	TTTCGCTCTGTCACC[C/T]AGGCTAGAGTACAGT	3993
rs796990387	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75560814	TATTAAAAAAAAAAA[A/T]AAAAAAAAAAAAAAA	3993
rs796995877	multinucleotide-polymorphism	GC/TA			intron-variant	LLGL2	GRCh38.p7	17:75527918	CAGCCTTCTGAGTAG[GC/TA]GGGACTACAAGCGCG	3993
rs796998174	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572308	CAGATCACAAGGGCA[A/G]GAGTTCGAGATCAGC	3993
rs797046054	in-del	-/TA			upstream-variant-2KB, frameshift-variant, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523735	GTGGCCACATTCCGA[-/TA]AAGAATAACCCTGGC	3993
rs797046055	in-del	-/C			upstream-variant-2KB, frameshift-variant, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523746	CCGAAAGAATAACCC[-/C]TGGCAAACCCTATGC	3993

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