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
rs936058	snp	C/T	0.47802	0.102502	intron-variant	LLGL2	GRCh38.p7	17:75571272	AGCTGACTCAGAGGC[C/T]GAGGCAGGGGAGGGG	3993
rs936059	snp	A/C	0.489492	0.0717183	intron-variant	LLGL2	GRCh38.p7	17:75569429	TCCACCGGAAAAGCA[A/C]AGGACACAGAATGTG	3993
rs936060	snp	C/T	0.385168	0.210309	intron-variant	LLGL2	GRCh38.p7	17:75563261	CCCATCGCCTGCACC[C/T]CATGCCTCTGCACAG	3993
rs936061	snp	A/G	0.0186639	0.0947819	intron-variant	LLGL2	GRCh38.p7	17:75558282	GGAAGCAGTGAAGGC[A/G]AGGAGGGCATGGAAG	3993
rs960511	snp	A/G	0.433236	0.170072	intron-variant	LLGL2	GRCh38.p7	17:75565337	CCCTTTCAGGCCAGC[A/G]TCATTAGGAGAGGGC	3993
rs960512	snp	C/G	0.433236	0.170072	intron-variant	LLGL2	GRCh38.p7	17:75565238	TGTCACACAATTTAC[C/G]AGGCTGACTCAGGGC	3993
rs1042861	snp	C/T	0.467919	0.122521	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574949	CACCGGCCTCTCCGG[C/T]TGGGGCAGGGACCCC	3993
rs1126939	snp	C/G	0.408695	0.193201	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574637	GCGTTCACATCGAGC[C/G]GCCGTGGGGTGCAGC	3993
rs1128126	snp	C/G/T	0.00013221	0.00812941	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524445	GGATGGAGCTTGCTC[C/G/T]GGGGGACCGGGACTG	3993
rs1470941	snp	A/G	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75562236	TAGCCCCATAAAACA[A/G]AACTCTGTGTGAGTT	3993
rs1620378	snp	A/G	0.497558	0.0348586	intron-variant	LLGL2	GRCh38.p7	17:75561462	tttttattttttgtg[A/G]ggagagacagggtct	3993
rs1626316	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75560747	tgtaatcccagcact[C/T]tgggaggctgaggcg	3993
rs1661712	snp	A/C	0.405033	0.196124	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574675	CACTCAAGCCCAGAG[A/C]CCCCACCTCCGCCAT	3993
rs1661713	snp	A/G	0.48818	0.0759629	intron-variant	LLGL2	GRCh38.p7	17:75572929	GGCCCTCCCCTCCCC[A/G]CATGCCTCCCGGTGT	3993
rs1661714	snp	A/G	0.357353	0.225777	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571974	CACTTCGAGGGGCTC[A/G]GGAAGGGGTACGCTG	3993
rs1661715	snp	A/G	0.400456	0.199657	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571765	GCTCTGCCCGCACAG[A/G]CTCATCCATTCTCCG	3993
rs1661716	snp	A/C	0.47802	0.102502	intron-variant	LLGL2	GRCh38.p7	17:75571454	AGGGAGAGACACGTC[A/C]TCTGGAGACCAGCAG	3993
rs1661718	snp	A/C	0.0910124	0.192936	intron-variant	LLGL2	GRCh38.p7	17:75571127	GCCCACTACCCCCTG[A/C]CCCCCAACCCCAGGC	3993
rs1661721	snp	A/C	0.34101	0.232846	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566796	CTCAGACTTGATCCC[A/C]GCCCAGCTGAGCTTG	3993
rs1661722	snp	A/G	0.426966	0.176587	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566340	tctttgctccactcc[A/G]tgtcccccacatggc	3993
rs1661723	snp	A/G	0.426047	0.177503	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566210	tctatacgatctggc[A/G]cTGGCCACATCTGGA	3993
rs1661725	snp	A/G	0.499801	0.00998203	intron-variant	LLGL2	GRCh38.p7	17:75564053	CAACTAAAGGAGTTT[A/G]AGACCTGCTGCTCAG	3993
rs1661727	snp	C/T	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75561647	AGGCGTGAGCCACCG[C/T]GCCCGGCCTAATTTT	3993
rs1661728	snp	C/T	0.387453	0.208822	intron-variant	LLGL2	GRCh38.p7	17:75560696	GAGTTCGAGACTAGT[C/T]TGACCACCATGGAGA	3993
rs1661729	snp	C/T	0.029116	0.117091	intron-variant	LLGL2	GRCh38.p7	17:75556944	cctcccaggttcaaa[C/T]gattctcccatctca	3993
rs1671016	snp	C/T	0.360548	0.22423	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574693	CAGCACGGTTGGCAG[C/T]TGCACTCAAGCCCAG	3993
rs1671018	snp	A/G	0.00183678	0.0302493	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574623	CCGCTCGATGTGAAC[A/G]CCAGTTGCCGCTCCT	3993
rs1671019	snp	A/C	0.479258	0.0997024	intron-variant	LLGL2	GRCh38.p7	17:75573846	CAGCCTGTCCTGAGC[A/C]GGAGAGCCTGGGAGG	3993
rs1671020	snp	C/T	0.427423	0.176128	intron-variant	LLGL2	GRCh38.p7	17:75572903	GGTGTCCTGACAAAC[C/T]CTTGGCTCTCAGATG	3993
rs1671021	snp	A/G	0.469911	0.118908	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569090	CGCCCTGGGCACTGA[A/G]GTTCTCGTTGGGGTC	3993
rs1671022	snp	C/T	0.338523	0.233803	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566357	Ctctcactgggctcc[C/T]gtctttgctccactc	3993
rs1671023	snp	C/T	0.424659	0.17887	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566135	GGAGCAAGCCAAGAG[C/T]CCTCCCAGCTCAGTC	3993
rs1671025	snp	C/T	0.432504	0.170857	intron-variant	LLGL2	GRCh38.p7	17:75564137	GCCACTCCTGCCTCA[C/T]GCTGGGTGCCCCCAC	3993
rs1671026	snp	C/T	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75564122	TGCTGGGTGCCCCCA[C/T]CAATTCTGTTTGAAC	3993
rs1671027	snp	C/T	0.388021	0.208447	intron-variant	LLGL2	GRCh38.p7	17:75563548	TACCCTCTCTGGCCC[C/T]GGAGTTTGCTTCAGA	3993
rs1671028	snp	C/T	0.382572	0.211954	intron-variant	LLGL2	GRCh38.p7	17:75563482	GGGGTGGGCCCTGCC[C/T]GGCGGGTGAAACACT	3993
rs1671029	snp	A/G	0.335101	0.23507	intron-variant	LLGL2	GRCh38.p7	17:75562680	TTGGGAGGCGGAGGC[A/G]GGAGAATTGCTTGAA	3993
rs1671031	snp	C/G	0.497586	0.0346604	intron-variant	LLGL2	GRCh38.p7	17:75560526	GCACTCTAGCCTGGG[C/G]AACAAGAGTGAAACT	3993
rs1671032	snp	C/T	0.497776	0.0332724	intron-variant	LLGL2	GRCh38.p7	17:75559824	TTTTAGCCACGGAGC[C/T]TGCGAGCAAATGGAA	3993
rs1671033	snp	C/G	0.49703	0.0384237	intron-variant	LLGL2	GRCh38.p7	17:75558442	ACACACTGGGGCCAC[C/G]CAGCCCCAGTTGTTT	3993
rs1671035	snp	A/G	0.439918	0.162576	intron-variant	LLGL2	GRCh38.p7	17:75557847	GATCCTGAGCTGCAA[A/G]AGACATGTTGGCTGT	3993
rs1671036	snp	C/T	0.499986	0.00264766	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556104	CCGATGGCCAGGATG[C/T]GCAGGGACGGGCTGT	3993
rs1671037	snp	A/G	0.0444908	0.142359	intron-variant	LLGL2	GRCh38.p7	17:75555955	CCAGACGACCCAGCA[A/G]GAAGCAGGGCTTCGG	3993
rs2017625	snp	A/G	0.493477	0.0567349	intron-variant	LLGL2	GRCh38.p7	17:75556985	CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT	3993
rs2305525	snp	C/T	0.388355	0.208294	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570480	TCCTGGGGGGCCAGC[C/T]GGGTGCCGCTTCCGG	3993
rs2305526	snp	A/T	0.20849	0.24653	intron-variant	LLGL2	GRCh38.p7	17:75569181	AGCAGCCACGGGGAC[A/T]GGACCCAGCTGGCCT	3993
rs2305527	snp	A/T	0.095934	0.196885	intron-variant	LLGL2	GRCh38.p7	17:75559504	GAATTCCCAGCAGAG[A/T]AATGACAGCTCCTGA	3993
rs2305528	snp	C/G	0.495135	0.0490805	intron-variant	LLGL2	GRCh38.p7	17:75555981	CCACCATGGCTGCTG[C/G]AGCTGCAGCACCAGA	3993
rs3785430	snp	C/T	0.335559	0.234904	intron-variant	LLGL2	GRCh38.p7	17:75565636	CTCAGCAAGTTTCTT[C/T]CCTCCCTTCCTGACC	3993
rs3862478	snp	C/T	0.497668	0.0340657	intron-variant	LLGL2	GRCh38.p7	17:75572844	AAAAAAAAATCCAGA[C/T]AGGGAAGTCGGTGAC	3993
rs3896707	snp	C/T	0.493523	0.0565391	intron-variant	LLGL2	GRCh38.p7	17:75556827	CATTGACCAGGCTGG[C/T]CTTGAACTCCTGACC	3993
rs3910704	snp	C/T	0.487746	0.0773096	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567943	TTTTTTTTCTTTTCT[C/T]GAGACAGGGTTTCAC	3993
rs4073421	snp	C/T	0.450609	0.149185	intron-variant	LLGL2	GRCh38.p7	17:75546115	CCTCCCCATCCCCTC[C/T]CTCTTTACTGCCCCA	3993
rs4073422	snp	C/T	0.450609	0.149185	intron-variant	LLGL2	GRCh38.p7	17:75545929	CTAAATAATCTACAA[C/T]GCACAGGACAGCCTC	3993
rs4076354	snp	C/T	0	0	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524870	CTATCCCGCGGGCTT[C/T]TCTCACTCTTAGATC	3993
rs4076967	snp	C/G	0.460813	0.134379	intron-variant	LLGL2	GRCh38.p7	17:75550243	CTGCAAAGGTACACA[C/G]AGCAACCCTGAATCG	3993
rs4077852	snp	C/T	0.392881	0.205147	intron-variant	LLGL2	GRCh38.p7	17:75549460	CCGTGCCCACCCTCC[C/T]CTGTCCCCTTAGGCC	3993
rs4788896	snp	C/T	0.295599	0.245806	intron-variant	LLGL2	GRCh38.p7	17:75532127	actctgtggcccagg[C/T]tggagtgcaatggca	3993
rs4788897	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541756	ttttttgagatactg[G/T]ttttgctctgttgcc	3993
rs4788898	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541777	CTCTGTTGCCCAGGC[C/T]GGAGTGCAATGGCCT	3993
rs4788900	snp	C/T	0.384785	0.210554	intron-variant	LLGL2	GRCh38.p7	17:75560956	cctgcctcagccttc[C/T]gagtagctgggatta	3993
rs4789208	snp	C/T	0.450483	0.149354	intron-variant	LLGL2	GRCh38.p7	17:75548079	GAATGCTCACTGGAG[C/T]GTTTCAGATTTTGAA	3993
rs4789209	snp	A/C/G	0.331874	0.236213	intron-variant	LLGL2	GRCh38.p7	17:75548267	TTTTACAGAAGGACA[A/C/G]TTTTTTTTTTCCTTT	3993
rs4789210	snp	C/T	0.444444	0.157135	intron-variant	LLGL2	GRCh38.p7	17:75548273	AGAAGGACAATTTTT[C/T]TTTTCCTTTTTTTTT	3993
rs4789211	snp	C/G	0.467744	0.122832	intron-variant	LLGL2	GRCh38.p7	17:75551088	ATCCCCTGGGAGACA[C/G]GTCATTTACACATGA	3993
rs4789212	snp	A/G	0.473909	0.111197	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551286	GCAGGGTGGCCTCAG[A/G]TCCATCATCTCCAAT	3993
rs4789213	snp	C/G	0.493568	0.0563433	intron-variant	LLGL2	GRCh38.p7	17:75556445	TGTCCTTTCAGGACC[C/G]TTCATGTGGTCTGCT	3993
rs5015927	snp	C/T	0.0295035	0.117819	intron-variant	LLGL2	GRCh38.p7	17:75559005	CCTCCATCTGCACCC[C/T]GCCTCCTCCATCCGC	3993
rs5822090	in-del	-/G	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75557438	TGGTTCTGGCCGACT[-/G]GGGGCTCCCAGTGTT	3993
rs5822091	in-del	-/A	0.477768	0.103061	intron-variant	LLGL2	GRCh38.p7	17:75572360	GACTACTAAAAATAC[-/A]AAAAAAAAATAGCCC	3993
rs6416848	snp	C/T	0.365439	0.221752	intron-variant	LLGL2	GRCh38.p7	17:75544752	GGTCAGCGCTCCCAA[C/T]GTGCCCTGCCATTTC	3993
rs6501821	snp	C/G	0.123798	0.215808	intron-variant	LLGL2	GRCh38.p7	17:75526740	AGTTCTCTTGAAGGG[C/G]CTACAGAGAGGATTC	3993
rs6501822	snp	A/G	0.265113	0.249543	intron-variant	LLGL2	GRCh38.p7	17:75543550	GGTTTTCGGCCAAGC[A/G]GCTCAGGCTGGGGCT	3993
rs6501823	snp	C/G	0.251859	0.249993	intron-variant	LLGL2	GRCh38.p7	17:75543714	TGGGACTTCTCATCT[C/G]AAGGCTTTCACTGGC	3993
rs6501824	snp	C/T	0.393619	0.204631	intron-variant	LLGL2	GRCh38.p7	17:75544532	CCCAACTTTGCCACA[C/T]AGAAGCTGGATGGCC	3993
rs6501825	snp	G/T	0.396364	0.202676	intron-variant	LLGL2	GRCh38.p7	17:75544774	TGCCATTTCTCTCTG[G/T]GTTTCTTAGCCTGTG	3993
rs6501826	snp	C/T	0.245346	0.249957	intron-variant	LLGL2	GRCh38.p7	17:75551661	CTGCCCGCCCTTGAC[C/T]TGTGGCCTGAGAGCC	3993
rs7208126	snp	A/C	0.393065	0.205018	intron-variant	LLGL2	GRCh38.p7	17:75545131	CCCCTGCCCCCTTGC[A/C]CCAAGTTCTGTCTGT	3993
rs7208430	snp	A/G	0.484138	0.0876334	intron-variant	LLGL2	GRCh38.p7	17:75548818	tggtctcctacagtg[A/G]tattttggggtggta	3993
rs7208892	snp	A/G	0.328148	0.237472	intron-variant	LLGL2	GRCh38.p7	17:75553966	ATAAACCTCTGGTGA[A/G]TTAGGATATCTACAG	3993
rs7209370	snp	C/T	0.484279	0.0872533	intron-variant	LLGL2	GRCh38.p7	17:75548130	gaccggtaagtataa[C/T]gcaaatattccgaaa	3993
rs7210253	snp	A/G	0.484066	0.0878235	intron-variant	LLGL2	GRCh38.p7	17:75548820	gtctcctacagtggt[A/G]ttttggggtggtatg	3993
rs7211129	snp	C/G	0.32153	0.239548	intron-variant	LLGL2	GRCh38.p7	17:75536492	CCGGGCCTAACTATT[C/G]CGTGTCTCTAGGGGG	3993
rs7211130	snp	C/G	0.32153	0.239548	intron-variant	LLGL2	GRCh38.p7	17:75536493	CGGGCCTAACTATTC[C/G]GTGTCTCTAGGGGGT	3993
rs7211793	snp	C/T	0.295343	0.245854	intron-variant	LLGL2	GRCh38.p7	17:75530398	tctcacgcctgtaat[C/T]ccagcactttgggag	3993
rs7214191	snp	C/T	0.483995	0.0880135	intron-variant	LLGL2	GRCh38.p7	17:75548742	gcctgggtgacagag[C/T]gagattctgtctcaa	3993
rs7214407	snp	A/C	0.0966517	0.197444	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524944	GTCGGAGGGGATGGG[A/C]CGTCGCAGGCTTCCC	3993
rs7219049	snp	A/G	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75555501	TCCCTTTCTGGGAAG[A/G]TGGTTGGAATTTGGT	3993
rs7219929	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75551144	TAGAGTCGCTGTGAA[A/G]GTCACTGCCCTTATT	3993
rs7222559	snp	C/G	0.0414363	0.137845	intron-variant	LLGL2	GRCh38.p7	17:75547908	AGGTGAATGAAGgtt[C/G]TCTTGTTATGCAGAG	3993
rs7222924	snp	G/T	0.484279	0.0872533	intron-variant	LLGL2	GRCh38.p7	17:75548096	tttcagattttgaaa[G/T]tttggatttgggatg	3993
rs7223552	snp	A/G	0.00664444	0.0572545	intron-variant	LLGL2	GRCh38.p7	17:75526859	TGGCCCAGCCCGGGG[A/G]AAGCCAAGGTCAGAA	3993
rs7224904	snp	C/T	0.272241	0.249009	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542143	CCACGCTGCCCAGAT[C/T]ACATGGGATCCTATC	3993
rs7225150	snp	G/T	0.135825	0.222405	intron-variant	LLGL2	GRCh38.p7	17:75530287	gagggaggattgctt[G/T]aacccaggagttcaa	3993
rs7225291	snp	A/G	0.0236746	0.106192	intron-variant	LLGL2	GRCh38.p7	17:75530389	ggcgcggtgtctcac[A/G]cctgtaattccagca	3993
rs7225594	snp	A/G	0.393065	0.205018	intron-variant	LLGL2	GRCh38.p7	17:75545001	GGGTCTCAAAGCTTC[A/G]GTGTCCACGGGAGAT	3993
rs7502310	snp	A/G	0.252421	0.249988	intron-variant	LLGL2	GRCh38.p7	17:75531507	ACTCATTTGTCCTCA[A/G]TCCTCAACTCTGAGA	3993
rs7502311	snp	A/G	0.25214	0.249991	intron-variant	LLGL2	GRCh38.p7	17:75531514	TGTCCTCAATCCTCA[A/G]CTCTGAGAGGCCCTC	3993
rs7502339	snp	A/C	0.250567	0.250298	intron-variant	LLGL2	GRCh38.p7	17:75531631	AGGAGCAGTTTGCAG[A/C]GAGAAAACTGGGGAC	3993
rs7502353	snp	G/T	0.456095	0.141508	intron-variant	LLGL2	GRCh38.p7	17:75549602	GAGGGCCAGGCTGCC[G/T]CCACTGCCAGGAATC	3993
rs7502597	snp	C/T	0.456095	0.141508	intron-variant	LLGL2	GRCh38.p7	17:75549920	CCTACTCCAGGCTAA[C/T]GTTGCAGTCTGGCGG	3993
rs7502603	snp	A/C	0.35894	0.225016	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542695	AGCACAGCCCATGAG[A/C]GCACAGGGAAGCTGG	3993
rs7502690	snp	A/C	0.485866	0.0828688	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542683	AGAACCTTTCTGAGC[A/C]CAGCCCATGAGCGCA	3993
rs7502880	snp	C/T	0.362313	0.223351	intron-variant	LLGL2	GRCh38.p7	17:75545924	CTGCGGAGGCTGTCC[C/T]GTGCGTTGTAGATTA	3993
rs7503721	snp	A/G	0.456095	0.141508	intron-variant	LLGL2	GRCh38.p7	17:75547592	cactttgggaggctg[A/G]ggtgggtggatcact	3993
rs8064529	snp	C/T	0.469183	0.120245	TSEN54, LLGL2, LOC107985023	17	allele_origin=T(germline)/C(germline)	17:75523332	TTCCTGATGGAGGTG[C/T]CCGGTAAGTTTCCAA	3993
rs8067210	snp	C/T	0.0962929	0.197165	intron-variant	LLGL2	GRCh38.p7	17:75526923	CTGTAATCCCAGCAC[C/T]TTGGGAAGCCAAGGC	3993
rs8070053	snp	C/T	0.137187	0.223099	intron-variant	LLGL2	GRCh38.p7	17:75532267	aattttttgtttgtt[C/T]tgagacggagacttg	3993
rs8070866	snp	A/T	0.121022	0.21416	intron-variant	LLGL2	GRCh38.p7	17:75531848	CCCTCTCTTCTTCCC[A/T]GGAACCACAGCGAAT	3993
rs8076354	snp	C/T	0.392696	0.205275	intron-variant	LLGL2	GRCh38.p7	17:75549684	AGTGCTCCCCCAAGG[C/T]GCTGGGCAGCCTCTG	3993
rs8078147	snp	A/G	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75559529	GAATTCCATGGGGCT[A/G]TAGCAGGGGAGGCTC	3993
rs9892893	snp	G/T	0.45889	0.13735	intron-variant	LLGL2	GRCh38.p7	17:75529589	aaaattaggccgggc[G/T]ctgtgtctcacgcct	3993
rs9901890	snp	A/G	0.392696	0.205275	intron-variant	LLGL2	GRCh38.p7	17:75545694	GTGAATAGTGGTCCC[A/G]TTTACAATGTAGGAA	3993
rs9902354	snp	A/G	0.494936	0.050064	intron-variant	LLGL2	GRCh38.p7	17:75531479	GCTGCTTTGAGCAGC[A/G]CTGGCAGCCTGGACT	3993
rs9908730	snp	C/G	0.456214	0.141336	intron-variant	LLGL2	GRCh38.p7	17:75549847	AGCCTTTGCCCACTC[C/G]CTCCCCTTCCGGGAC	3993
rs9909269	snp	G/T	0.0193772	0.0965046	intron-variant	LLGL2	GRCh38.p7	17:75548786	gccaaagaagtatac[G/T]ttggggtagcccatt	3993
rs9910576	snp	C/T	0.456095	0.141508	intron-variant	LLGL2	GRCh38.p7	17:75549906	GACGGGCCTTCTCCC[C/T]TACTCCAGGCTAACG	3993
rs9910589	snp	G/T	0.454182	0.144256	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542142	CCCACGCTGCCCAGA[G/T]TACATGGGATCCTAT	3993
rs9911128	snp	A/G	0.456332	0.141164	intron-variant	LLGL2	GRCh38.p7	17:75549762	CAGGGACTCCTCCTC[A/G]GGTCCTAGCCCTTGG	3993
rs9911632	snp	C/T	0.00112035	0.0236415	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573227	TACAGCTGCATCCGC[C/T]GGGAGGACGTCAGTG	3993
rs9912509	snp	A/C	0.454423	0.143914	intron-variant	LLGL2	GRCh38.p7	17:75550754	CCACTGCACTCCAGC[A/C]TGGGCAACAGAGTGA	3993
rs9913780	snp	C/G	0.471863	0.115225	intron-variant	LLGL2	GRCh38.p7	17:75529603	CTCTGTGTCTCACGC[C/G]TGTAATCCCAGCACT	3993
rs10526094	in-del	-/ACACACACACACAC/ATACACACACACAC			intron-variant	LLGL2	GRCh38.p7	17:75532055	TATATATGTATATAT[lengthTooLong]ACACACACACACACA	3993
rs10648915	in-del	-/CT	0.479388	0.0994042	intron-variant	LLGL2	GRCh38.p7	17:75573695	CCTCTCTGAGATACC[-/CT]GAGGCTCCCACTGCT	3993
rs10674349	in-del	-/AA	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75527184	AAAAAAAAAAAAAAA[-/AA]GTGGCATTTGAGGAA	3993
rs10691517	in-del	-/CT	0.452842	0.146134	intron-variant	LLGL2	GRCh38.p7	17:75561210	CCTTTAGTCTCATAA[-/CT]CTGTCTCTGAGAAGT	3993
rs11077793	snp	A/C	0.484701	0.0861117	intron-variant	LLGL2	GRCh38.p7	17:75552782	ATACTTGAAGGGTTT[A/C]CAAGAACTGACTTAA	3993
rs11077794	snp	G/T	0.0955749	0.196603	intron-variant	LLGL2	GRCh38.p7	17:75562384	ACTTTGATGCCCTCC[G/T]GAGGTCTTATGCACC	3993
rs11649969	snp	G/T	0	0	intron-variant	LLGL2	GRCh38.p7	17:75534717	aactcctaggttcag[G/T]ggattctcctgcctc	3993
rs11651803	snp	A/C	0.494609	0.0516363	intron-variant	LLGL2	GRCh38.p7	17:75553978	TGAATTAGGATATCT[A/C]CAGGTAAAGAATATT	3993
rs11652563	snp	A/G	0.490673	0.0676508	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542595	GTGGGCGGAGAGTTT[A/G]GGGGCCTTGAGCTGG	3993
rs11652614	snp	A/T	0.357877	0.225527	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542720	AGCTGGACTGGGGCT[A/T]GCCAGAGAGAGGGGA	3993
rs11653024	snp	C/T	0.494568	0.0518327	intron-variant	LLGL2	GRCh38.p7	17:75554409	ttgagtctagaaggt[C/T]aagaccaggctggac	3993
rs11653056	snp	C/T	0.328148	0.237472	intron-variant	LLGL2	GRCh38.p7	17:75554471	taaaaagtagccggg[C/T]gtggcaggtgtggtg	3993
rs11654903	snp	A/T	0.0256215	0.110247	intron-variant	LLGL2	GRCh38.p7	17:75543834	ggcacagggttgtca[A/T]ggaggttTAGGGACG	3993
rs11655620	snp	C/T	0	0	intron-variant	LLGL2	GRCh38.p7	17:75548392	aagggattctccagc[C/T]tcagcctcccacata	3993
rs11656381	snp	A/G	0.494484	0.0522255	intron-variant	LLGL2	GRCh38.p7	17:75554580	aaccgaaatcatgcc[A/G]tagcacccagcctgg	3993
rs11656570	snp	C/T	0.485255	0.0845871	intron-variant	LLGL2	GRCh38.p7	17:75554364	cgcctgtaatcccag[C/T]gctttgggaggccga	3993
rs11656574	snp	C/T	0.483852	0.0883933	intron-variant	LLGL2	GRCh38.p7	17:75554377	agcgctttgggaggc[C/T]gaggcaggaggatcg	3993
rs11657693	snp	C/T			synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570004	GGCAGCGGAGCAGGC[C/T]GTGGAGCAGGTGGAG	3993
rs11868111	snp	A/G	0.000365929	0.0135215	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570146	CAGTGTCAGCCCCCG[A/G]CTGTGGTCACCTCCT	3993
rs11868269	snp	A/T	0.116838	0.211584	intron-variant	LLGL2	GRCh38.p7	17:75554115	aagaccagcctggcc[A/T]acatggtgaaagccc	3993
rs11870627	snp	C/G	0.0387683	0.133721	LLGL2, TSEN54, LOC107985023	17	allele_origin=G(germline)/C(germline)	17:75524404	TTGCCCCAGGATGTG[C/G]GGCACTGACCTCACA	3993
rs11870956	snp	C/G	0.326506	0.238006	intron-variant	LLGL2	GRCh38.p7	17:75537021	AGAGACGGGGTTTTG[C/G]CATGTTGGCCAGGCT	3993
rs12449601	snp	C/T	0.156319	0.231784	intron-variant	LLGL2	GRCh38.p7	17:75551694	GCAAAAAGTTACAGG[C/T]TGTTTTCTCTGTGGC	3993
rs12450232	snp	A/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75560803	GTTTGTTTATTTATT[A/T]aaaaaaaaaaaaaaa	3993
rs12451123	snp	A/G	0.477937	0.102688	intron-variant	LLGL2	GRCh38.p7	17:75552062	tgaacccgggaggtg[A/G]aggttgcagcgagct	3993
rs12451129	snp	C/T	0.125182	0.216612	utr-variant-3-prime, intron-variant	LLGL2	GRCh38.p7	17:75564652	AGGATCGCTTGAACC[C/T]AGGAGTTCAAGTCCA	3993
rs12453120	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528718	actccagcctgagca[A/G]caagagcaaaactcc	3993
rs12943627	snp	C/T	0.484279	0.0872533	intron-variant	LLGL2	GRCh38.p7	17:75548118	tttgggatgctcgac[C/T]ggtaagtataatgca	3993
rs12949844	snp	A/G	0.425432	0.178112	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567955	CTCGAGAAAAGAAAA[A/G]AAAAAAAAAAGACAA	3993
rs12951026	snp	A/G	0.471004	0.116864	intron-variant	LLGL2	GRCh38.p7	17:75547692	cagttgggtgtggtg[A/G]cacacgcctgtagtc	3993
rs16968009	snp	A/G	0.159134	0.233407	intron-variant	LLGL2	GRCh38.p7	17:75569507	TCTTCTCCAGAAATC[A/G]GAATTAAGGGCTGGG	3993
rs28367187	snp	A/G	0.0962929	0.197165	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523503	TGTCTAGGGAAGAGG[A/G]AGAATAACCAGTGGG	3993
rs28406696	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75548496	TTCTGAGAATAACCA[A/G]CTCAAAGTATGCCAA	3993
rs28520001	snp	A/G/T	0.000636087	0.0178224	intron-variant	LLGL2	GRCh38.p7	17:75571122	GGCCAGCCTGGGGTT[A/G/T]GGGGGCAGGGGGTAG	3993
rs28573350	snp	A/G	0.327445	0.237702	intron-variant	LLGL2	GRCh38.p7	17:75554404	ATCGCTTGAGTCTAG[A/G]AGGTTAAGACCAGGC	3993
rs28676584	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75571120	GTGGCCAGCCTGGGG[G/T]TGGGGGGCAGGGGGT	3993
rs28753382	snp	C/G			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575589	TACCCAAGGAGAAAG[C/G]CCTTCCCCAGGGGAG	3993
rs33986841	in-del	-/A			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564862	GCCAGACTGTGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs34001927	snp	A/G	0.357593	0.225663	intron-variant	LLGL2	GRCh38.p7	17:75568881	TCTTCCCAGTAGGAT[A/G]TGTGGGGTGGGAGCA	3993
rs34106241	multinucleotide-polymorphism	CC/GG	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75536492	CCGGGCCTAACTATT[CC/GG]GTGTCTCTAGGGGGT	3993
rs34158726	snp	G/T	0	0	intron-variant	LLGL2	GRCh38.p7	17:75535156	GCAGGGGTCAGCAGC[G/T]GCCTCTGTGGTTTAG	3993
rs34158736	snp	C/T	0.0375726	0.131813	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563360	CTGGTGGCAGCGGGA[C/T]GGCCGCCTGCTCGTC	3993
rs34231839	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75532408	GCGCCCGCCACCACG[-/G]CCCAGCTAATTTTTT	3993
rs34255252	snp	C/T	0.00246242	0.0350021	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571670	GCTTCTCGGCAGGCT[C/T]CCGGCACTGCCCCTC	3993
rs34351197	snp	A/G	0.463343	0.130326	intron-variant	LLGL2	GRCh38.p7	17:75549941	AGTCTGGCGGCTTCT[A/G]CAAATCTTTGCTCTC	3993
rs34354968	in-del	-/G			frameshift-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573205	CCTGCTCAAGCCCCA[-/G]GTGCGCTACAGCTGC	3993
rs34430025	in-del	-/G	0.386884	0.209196	intron-variant	LLGL2	GRCh38.p7	17:75560426	GGGAATCTAGTCGGC[-/G]GGGGGGGCCCAAGTG	3993
rs34478905	snp	A/G	0.426201	0.177351	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567661	AAAGAGAAAAAAAAG[A/G]CTGGGCACAGTGGCT	3993
rs34545262	snp	A/G	0.000349883	0.0132219	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572044	CACCAGCTGCTCGTC[A/G]TATCAGAGGAGCAGT	3993
rs34553577	snp	A/G	0.000399454	0.0141268	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564429	ATCTCAGTGATCCAC[A/G]ATGGCCAGCAGACGG	3993
rs34638571	in-del	-/A	0	0	intron-variant	LLGL2	GRCh38.p7	17:75547825	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAATG	3993
rs34754454	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75559729	CAGGGGCTCCGCAGC[-/G]GGGGAAGTCGGGCCC	3993
rs34809387	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75547343	TAGTGGTTAGGGGCA[-/G]GGGACTTTGCAGCCA	3993
rs34810865	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75532197	CTCCCACCTCAGCCT[-/C]CCCCAGTAGCTGGGA	3993
rs34925878	in-del	-/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566867	GCTGAGTAGACAACT[-/G]GGGGCTTATGGGTCT	3993
rs34941161	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75550986	CCTGTTCCCAACAAG[-/A]ATCCCTTGGGCTTCT	3993
rs34987935	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75534003	AAGCTTCTTGGGACA[C/G]CTGTTCCAGTTTTAG	3993
rs34997179	snp	A/G	0.110872	0.20771	intron-variant	LLGL2	GRCh38.p7	17:75560178	CGTCTGCCCAGGGCA[A/G]GGCATGACTGGGCTG	3993
rs35093418	snp	C/T	0.497416	0.0358495	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567332	GCCAGGCATTGGTGG[C/T]ATGTGCCTGTAATCC	3993
rs35147087	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75552978	GCTGCCTCTGCTGCT[-/G]GGGAAAGTGCTGCTG	3993
rs35199943	snp	C/T	0.278399	0.248382	intron-variant	LLGL2	GRCh38.p7	17:75574761	TGGGTCCCACGGGGC[C/T]GACACGTGCCCTGAT	3993
rs35218854	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75548755	GTGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs35252272	in-del	-/T	0.388021	0.208447	intron-variant	LLGL2	GRCh38.p7	17:75562132	CCTGCTGCCTTGTGG[-/T]TTTTTTTGTTGGCTG	3993
rs35452644	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75530660	AAAAAAAAAAAAAAA[-/A]TTAGCTGGGCATCGT	3993
rs35474687	snp	A/G	0.00221308	0.033191	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571733	ATGCCTTCTCCCTGC[A/G]TGTGCCTCCCGCCGA	3993
rs35685683	in-del	-/C/CC			intron-variant	LLGL2	GRCh38.p7	17:75573693	GCCCTCTCTGAGATA[-/C/CC]CCGAGGCTCCCACTG	3993
rs35687632	snp	G/T	0.110167	0.207236	intron-variant	LLGL2	GRCh38.p7	17:75570704	CAGTAACTGTAATGC[G/T]TATCCTAGAAGTAAT	3993
rs35724508	in-del	-/A	0.485933	0.0826777	intron-variant	LLGL2	GRCh38.p7	17:75552128	GTCTTTAAAAAAAAA[-/A]GTCTAGAAGCTGCAT	3993
rs35886912	snp	A/G	0.0260766	0.111168	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574614	TGCCTGTGCAGGAGC[A/G]GCAACTGGCGTTCAC	3993
rs35940109	snp	C/T	0.0220515	0.102662	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558203	GCACCAGGAGAACAA[C/T]GCTGTGACGCAGATC	3993
rs35969651	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75565441	GTTCAGGGGAACCCC[-/A]AAACCTGCTTTTCTT	3993
rs35973733	snp	C/G/T	0.360632	0.224189	intron-variant	LLGL2	GRCh38.p7	17:75558978	CCCGCCTCCTCCATC[C/G/T]GCACCCCGCCTCCTC	3993
rs35991442	snp	C/T	0.00905418	0.0666717	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569119	CGAGGACGAGTGGCC[C/T]CCACTCCGCAAGGTG	3993
rs55649536	in-del	-/TTTTTTTTTTTT			intron-variant	LLGL2	GRCh38.p7	17:75557048	ACTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GTGGAGACAGGGTCT	3993
rs55691958	snp	A/G	0.137187	0.223099	intron-variant	LLGL2	GRCh38.p7	17:75532517	CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT	3993
rs55738577	snp	G/T	0.472429	0.114129	intron-variant	LLGL2	GRCh38.p7	17:75547108	TTTTTGTCCAACACC[G/T]TTTGGCTCAACTCCT	3993
rs55789626	snp	C/T	0.362313	0.223351	intron-variant	LLGL2	GRCh38.p7	17:75547110	TTTGTCCAACACCTT[C/T]TGGCTCAACTCCTTT	3993
rs55829007	snp	G/T	0.0205886	0.09935	intron-variant	LLGL2	GRCh38.p7	17:75558286	CATGCCCTCCTTGCC[G/T]TCACTGCTTCCAGCA	3993
rs55942748	snp	A/C/T			intron-variant	LLGL2	GRCh38.p7	17:75532078	CACACACACACACAC[A/C/T]TTTTTTTTTTTTTTT	3993
rs56054013	snp	C/T	0.472335	0.114312	intron-variant	LLGL2	GRCh38.p7	17:75547097	CAGTTCTGGCCTTTT[C/T]GTCCAACACCTTTTG	3993
rs56075222	snp	G/T	0.137527	0.223271	intron-variant	LLGL2	GRCh38.p7	17:75539275	TATGTTGCCCTGGCT[G/T]GTCTTGAACTCCTGA	3993
rs56183450	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532079	ACACACACACACACT[C/T]TTTTTTTTTTTTTTT	3993
rs56221020	snp	C/G	0.472522	0.113946	intron-variant	LLGL2	GRCh38.p7	17:75547173	GCAAGGACATCGCCC[C/G]GGGGGTCCTGAGAGG	3993
rs56326161	snp	A/G	0.140581	0.224783	intron-variant	LLGL2	GRCh38.p7	17:75532528	TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCGGC	3993
rs56338746	snp	G/T	0.140581	0.224783	intron-variant	LLGL2	GRCh38.p7	17:75539167	AGGCTCAGCAATCCT[G/T]CCACCTTAGCCTTTT	3993
rs56379615	snp	A/G	0.438946	0.163706	intron-variant	LLGL2	GRCh38.p7	17:75550826	CACACAAACTAGGGG[A/G]CAACTGGGGCACAGC	3993
rs56656168	in-del	-/T	0	0	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541746	TTTTTTTTTTTTTTT[-/T]GAGATACTGTTTTTG	3993
rs57392288	snp	C/T	0.400682	0.199487	intron-variant	LLGL2	GRCh38.p7	17:75532055	ATATATATGTATATA[C/T]ACACACACACACACA	3993
rs57400426	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530648	GAGCGAGACTCCATT[C/T]CAAAAAAAAAAAAAA	3993
rs57482643	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75550804	AAAAAAAAAAAAAAA[-/A]CACACACACACAAAC	3993
rs57591306	snp	A/G	0.122064	0.214785	intron-variant	LLGL2	GRCh38.p7	17:75535024	TGCCTTTCAGCCAAG[A/G]TTTGGTTGCTAAGCT	3993
rs58220046	in-del	-/ACACAC/ACACACACACACA/ACACACACACACACA/ACACACACACACACAC/ACACACACACACACACT/ACACACACACACACT/ACACACACACT			intron-variant	LLGL2	GRCh38.p7	17:75532077	CACACACACACACAC[lengthTooLong]TTTTTTTTTTTTTTT	3993
rs58275565	snp	A/G	0.248188	0.249993	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541456	GGGGCTTTCCCAGCC[A/G]GTGCCTGTTCTCTGA	3993
rs58360025	snp	C/T	0.17332	0.23795	intron-variant	LLGL2	GRCh38.p7	17:75545781	TAGGAGACATTGCCC[C/T]GACTAAGATAGGTGA	3993
rs58631882	snp	G/T	0.330482	0.236691	intron-variant	LLGL2	GRCh38.p7	17:75538665	TTAATAAGTAAGCTA[G/T]TCAGTGTGTCCAAAC	3993
rs58694058	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75554903	AAAAAAAAAAAAAAA[-/A]TTTTTGGCTGGGTGC	3993
rs59138015	snp	A/G	0.420415	0.182917	intron-variant	LLGL2	GRCh38.p7	17:75548858	TTCCAACAGCATCAT[A/G]ATGATCCCTAAGGGA	3993
rs59495109	in-del	-/A/AG			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564879	AAAAAAAAAAAAAAA[-/A/AG]GGGCTCTGCACAGAT	3993
rs59541498	snp	A/G	0.438246	0.16451	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542062	TCACCCTCCCAGCAC[A/G]GCAAGCCCTCGGTTC	3993
rs59767963	snp	C/T	0.150667	0.229419	intron-variant	LLGL2	GRCh38.p7	17:75571565	TGTCAGAGAGCCTTC[C/T]AGCCTCTCCCAGGAG	3993
rs59997228	in-del	-/C	0.246485	0.249975	intron-variant	LLGL2	GRCh38.p7	17:75540050	GGGAGGGAGTGCCAT[-/C]TCCCCCTTTACAGAG	3993
rs60056143	snp	C/T	0.246485	0.249975	intron-variant	LLGL2	GRCh38.p7	17:75540086	TCTCTGGAGGCCATG[C/T]GGCTTGGGGGAGCTA	3993
rs60263689	snp	C/G	0.0433133	0.140645	intron-variant	LLGL2	GRCh38.p7	17:75563211	CATGGCAGGCGCCAT[C/G]TTGCTCTCCCAGGGC	3993
rs60531093	in-del	-/AAA	0.483126	0.0902898	intron-variant	LLGL2	GRCh38.p7	17:75548756	GTGAGATTCTGTCTC[-/AAA]AAAAAAAAAAAAGCC	3993
rs60685279	in-del	-/TT	0.296619	0.245615	intron-variant	LLGL2	GRCh38.p7	17:75529147	GCAATAGAGTGAGAC[-/TT]TGTCTCAAAAAAAAA	3993
rs60884992	in-del	-/AA			intron-variant	LLGL2	GRCh38.p7	17:75550803	AAAAAAAAAAAAAAA[-/AA]CACACACACACAAAC	3993
rs60926865	snp	C/G	0.195837	0.244062	intron-variant	LLGL2	GRCh38.p7	17:75544238	ATGATCTTCTCACCT[C/G]TGCTTTGCGCCTCTG	3993
rs61400258	in-del	-/A			intron-variant	LLGL2	GRCh38.p7	17:75554320	AAAAAAAAAAAAAAA[-/A]GCCATTTTAGGCAGC	3993
rs61412770	snp	C/T	0.245916	0.249967	intron-variant	LLGL2	GRCh38.p7	17:75532162	TTCGGCTCACTGCAG[C/T]CTCCCCAGGTTCAAG	3993
rs61539483	snp	C/T	0.0142736	0.0832652	intron-variant	LLGL2	GRCh38.p7	17:75528146	TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG	3993
rs61640974	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75530649	AGCGAGACTCCATTT[A/C]AAAAAAAAAAAAAAA	3993
rs61683299	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557956	TCTCCCAGGGATCAG[A/G]TCACTGGCCTGGTGC	3993
rs61690658	snp	A/G	0.245916	0.249967	intron-variant	LLGL2	GRCh38.p7	17:75533406	GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	3993
rs61739417	snp	C/T	0.000274297	0.0117078	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571668	TGGCTTCTCGGCAGG[C/T]TCCCGGCACTGCCCC	3993
rs61744731	snp	A/C/G	0.00395064	0.0442692	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559365	AGCTGCCAGCTTTTC[A/C/G]TGCGCTGGAGGACCG	3993
rs61751715	snp	A/G/T	5.31442e-05	0.00515459	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574638	CGTTCACATCGAGCC[A/G/T]CCGTGGGGTGCAGCC	3993
rs62088469	snp	C/T	0.288906	0.246954	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523508	AGGGAAGAGGGAGAA[C/T]AACCAGTGGGTTAGC	3993
rs62088470	snp	C/G	0.110088	0.207182	LLGL2, TSEN54, LOC107985023	17	allele_origin=G(germline)/C(germline)	17:75524278	TTTGATGAGCCTGTC[C/G]CAGACCTCTGCAGCC	3993
rs62088471	snp	G/T	0.178144	0.239451	intron-variant	LLGL2	GRCh38.p7	17:75528060	AGTGTTAGGATTACA[G/T]GCATGAACTGCCACG	3993
rs62088473	snp	A/G	0.196149	0.244131	intron-variant	LLGL2	GRCh38.p7	17:75534742	TGCCTCGACCTCCCA[A/G]AGTGCTGGGATTACA	3993
rs62088474	snp	A/G	0.245916	0.249967	intron-variant	LLGL2	GRCh38.p7	17:75535468	CCAGCAGATCAATGA[A/G]ATCAATGGAACTTCC	3993
rs62088475	snp	A/G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535932	GGAAGGAAACAGGTC[A/G/T]ATCAGCTGCCCACAG	3993
rs62088476	snp	A/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75535968	TCTCAGGCTGGTTCC[A/G]CATGCAAGGCACAGA	3993
rs62088477	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75536408	GATGGAATAGAAAAG[A/T]CCTTTCTACTCAGGA	3993
rs62088478	snp	A/G	0.241053	0.24984	intron-variant	LLGL2	GRCh38.p7	17:75536471	CCTGCCTGTCTCCCC[A/G]CCTTTCCGGGCCTAA	3993
rs62088534	snp	A/C	0.406641	0.194842	intron-variant	LLGL2	GRCh38.p7	17:75537522	AATATGGTGAAAACC[A/C]CAGCTCTACTAAAAA	3993
rs62088535	snp	C/T	0.2462	0.249971	intron-variant	LLGL2	GRCh38.p7	17:75538090	TGCTGGGATTACAGG[C/T]GTGAGCCACCTCGCC	3993
rs62088536	snp	C/T	0.2462	0.249971	intron-variant	LLGL2	GRCh38.p7	17:75538123	GCCTGGAAGGGGGGC[C/T]GGGCTGATTGAGGGG	3993
rs62088537	snp	C/T	0.343254	0.231956	intron-variant	LLGL2	GRCh38.p7	17:75538404	AAGCCTCTCTCATCT[C/T]GAGGCTTTGCAGCTG	3993
rs62088539	snp	A/G	0.192401	0.243274	intron-variant	LLGL2	GRCh38.p7	17:75539005	TCCACTGATCTTCCC[A/G]CCTCAGCCTCCCAAG	3993
rs62088541	snp	A/G	0.176861	0.239062	intron-variant	LLGL2	GRCh38.p7	17:75540858	CTCACAAACTCACAC[A/G]GTGCCAAGGAAAGGA	3993
rs62088544	snp	A/G	0.215446	0.2476	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542086	TCGGTTCCTCTGCCC[A/G]AAGACACCCCCAACT	3993
rs62088545	snp	C/T	0.416055	0.186885	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542237	ACCTCAGCTTAGATA[C/T]CTTCTTCTCGAAGGT	3993
rs62088546	snp	C/T	0.451483	0.148002	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543304	GCAGCCTACTGGACT[C/T]GGAGAGAGAGGCCCT	3993
rs62088547	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75544008	TCCTTCTGGCTCCGG[A/C]CGGGGTGAGTGGGGA	3993
rs62088549	snp	A/G	0.400325	0.199756	intron-variant	LLGL2	GRCh38.p7	17:75546590	AGGTCCAGCAGACAG[A/G]CGGAGGGCAGGTCCA	3993
rs62088550	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75546656	GAGGGCAGGTCCAGC[A/G]GACAGGCGGAGGGCA	3993
rs62088551	snp	C/G	0.453453	0.145282	intron-variant	LLGL2	GRCh38.p7	17:75546918	AGCGGCACGTGGGCT[C/G]TTGGTGTAGGCGAGG	3993
rs62088555	snp	A/C	0.483995	0.0880135	intron-variant	LLGL2	GRCh38.p7	17:75548307	TTTTGGACGGAGTTT[A/C]GCTCTTGTTGCCCGG	3993
rs62088556	snp	A/G	0.483995	0.0880135	intron-variant	LLGL2	GRCh38.p7	17:75548403	CAGCCTCAGCCTCCC[A/G]CATAGCTGGGATTAC	3993
rs62088558	snp	A/G	0.249603	0.25	intron-variant	LLGL2	GRCh38.p7	17:75552982	GCCTCTGCTGCTGGG[A/G]AAGTGCTGCTGTCCT	3993
rs62089183	snp	A/G	0.481932	0.0933148	intron-variant	LLGL2	GRCh38.p7	17:75555119	GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATCGCA	3993
rs62089184	snp	C/T	0.00953873	0.0683987	intron-variant	LLGL2	GRCh38.p7	17:75556267	GACTTTCCTGATTTC[C/T]AGTTTTGGACATGAT	3993
rs62089185	snp	A/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75556269	CTTTCCTGATTTCCA[A/G]TTTTGGACATGATTT	3993
rs62089187	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75572823	AGACTCCATCTCGGA[A/G]GAAAAAAAAAAAAAT	3993
rs66614718	snp	C/T	0.254723	0.249955	intron-variant	LLGL2	GRCh38.p7	17:75558675	CAGCCCAGCCTGACC[C/T]TTGCCCTTAGCTCTG	3993
rs66620492	in-del	-/T	0.47023	0.118317	intron-variant	LLGL2	GRCh38.p7	17:75530646	CAGAGCGAGACTCCA[-/T]TTCAAAAAAAAAAAA	3993
rs66986045	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75573696	CTCTCTGAGATACCG[-/CT]AGGCTCCCACTGCTG	3993
rs66990038	snp	A/G	0.311369	0.242351	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526022	AGAAAGTTCTGCGGG[A/G]AACTTCTCTGCCTGA	3993
rs71161230	in-del	-/TTTT	0	0	intron-variant	LLGL2	GRCh38.p7	17:75572681	CCACCACCATGCTGG[-/TTTT]TTTTTTTTTTTTTTT	3993
rs71361685	multinucleotide-polymorphism	GC/TT	0.5	0	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542142	CCCACGCTGCCCAGA[GC/TT]ACATGGGATCCTATC	3993
rs71361686	in-del	-/A	0.375	0.216506	intron-variant	LLGL2	GRCh38.p7	17:75560837	AAAACAAAGAAAAAA[-/A]CATTTTTTTTGAGAG	3993
rs71382171	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75535213	TAGGAGGTGCAGGGG[C/T]GGATTCACATCCGTC	3993
rs71382172	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75556686	TCTGTGCCCCTGCCT[C/T]CCTCAGCTCCCCACC	3993
rs71382173	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75570827	GTCCCTCTAGACGCA[A/G]GCCTGGCAGGTGGCT	3993
rs71383066	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558966	CTCCATCCGCACCCC[A/G]CCTCCTCCATCCGCA	3993
rs71383067	snp	A/G	0.375	0.216506	intron-variant	LLGL2	GRCh38.p7	17:75558979	CCGCCTCCTCCATCC[A/G]CACCCCGCCTCCTCC	3993
rs71383068	snp	A/C	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558984	TCCTCCATCCGCACC[A/C]CGCCTCCTCCATCTG	3993
rs71761125	in-del	-/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541716	GGGATGTGGCTCTGC[-/T]TTTTTTTTTTTTTTT	3993
rs72439797	in-del	-/AAAAAAAA	0.428484	0.175052	intron-variant	LLGL2	GRCh38.p7	17:75554303	GCAAAACTCCGTCTC[-/AAAAAAAA]AAAAAAAAAAGCCAT	3993
rs72851947	snp	A/G	0.133777	0.221342	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523587	CTTCCTGGAACTGGT[A/G]GAGGGAAAGGGTGGG	3993
rs72851953	snp	A/G	0.136506	0.222754	intron-variant	LLGL2	GRCh38.p7	17:75539566	TTTTTTTGATCAGAG[A/G]TAGTCCTGACCTCTG	3993
rs72851955	snp	A/G	0.00557542	0.0525036	intron-variant	LLGL2	GRCh38.p7	17:75541204	TGGAGTCTTTGGCAC[A/G]GATGGCCCTGTGCCC	3993
rs72851957	snp	C/T	0.136166	0.22258	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541512	GGGCCCTAGGAGTTT[C/T]CCGGCCACCTGCTCT	3993
rs72854915	snp	A/G	0.00716266	0.059414	intron-variant	LLGL2	GRCh38.p7	17:75562479	CCTTATAATTGTACC[A/G]CCTGTGTTTACATCA	3993
rs72854916	snp	A/G	0.0337553	0.125452	intron-variant	LLGL2	GRCh38.p7	17:75565409	CTGGTCTGTGTACTC[A/G]CGGCCTCTATCTACC	3993
rs72859222	snp	A/G	0.00716266	0.059414	intron-variant	LLGL2	GRCh38.p7	17:75546045	CTGAGGGGTAAAATC[A/G]CTCCTGGTTTGAGAC	3993
rs72859224	snp	C/T	0.480853	0.0959518	intron-variant	LLGL2	GRCh38.p7	17:75546917	GAGCGGCACGTGGGC[C/T]GTTGGTGTAGGCGAG	3993
rs72859227	snp	A/G	0.0333695	0.124785	intron-variant	LLGL2	GRCh38.p7	17:75550062	GGTAGGCTGGATGCC[A/G]CGCTTCGGAGGCCCC	3993
rs73362268	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533669	ATCCTTAAACAAAGC[A/C]AAGATGTCTGCCGTC	3993
rs73362282	snp	C/T	0.248188	0.249993	intron-variant	LLGL2	GRCh38.p7	17:75539119	GCTAGAGTACAGTGG[C/T]GGGTTCATAGCTCAC	3993
rs73362284	snp	C/G	0.247337	0.249986	intron-variant	LLGL2	GRCh38.p7	17:75539405	TAAATTTGAAAAAAT[C/G]TCCTTTCCTTTTTTT	3993
rs73362295	snp	C/T	0.118584	0.212673	intron-variant	LLGL2	GRCh38.p7	17:75544156	CAGGACGGGCCTGTA[C/T]GCAGGAGGCGTGCAG	3993
rs73364218	snp	A/C	0.177503	0.239258	intron-variant	LLGL2	GRCh38.p7	17:75550226	TGTCCTGAGTGCAGC[A/C]GCGATTCAGGGTTGC	3993
rs73364265	snp	C/T	0.0402167	0.135981	intron-variant	LLGL2	GRCh38.p7	17:75572103	CTCCCTGGGACTCCC[C/T]GGGACATCCAGGAGG	3993
rs73998313	snp	A/T	0.00795532	0.062565	intron-variant	LLGL2	GRCh38.p7	17:75539929	TCATCCCATTTTCTG[A/T]TTTGTGTCCTGTGAA	3993
rs73998338	snp	A/C	0.00697989	0.058662	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574531	GCTGGGGTGGGCCCG[A/C]GGCTCTGCCAGAGGG	3993
rs74459945	snp	A/G	0.040671	0.13668	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551300	GATCCATCATCTCCA[A/G]TCCAAGGACAGCTCT	3993
rs74477521	snp	C/T	0.151334	0.229706	intron-variant	LLGL2	GRCh38.p7	17:75565728	GTGTCCCCAACTCCC[C/T]GCAGTCCCGCAGGCC	3993
rs74512764	snp	C/T	0.0154538	0.0865337	intron-variant	LLGL2	GRCh38.p7	17:75549343	CCAGCTCGCTCCCCT[C/T]GGCCAAACCCAGGCA	3993
rs74520907	snp	C/G	0.178144	0.239451	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525477	TTCTGCGTCCAGGTG[C/G]GCGCAGGTGAGGCCG	3993
rs74693238	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75545385	AATCTGATTAGGCCT[C/T]TGCCCTCCACTTTTA	3993
rs74759582	snp	C/G	0.152001	0.229992	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575396	CGGTGCCTTCCCTCT[C/G]TGGGAACACATGGCA	3993
rs74785377	snp	C/T	0.0158915	0.0877111	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574413	TGTGGCTAGCCGCCC[C/T]AAGGGCCTCAGTGGG	3993
rs74876688	snp	C/T	0.00125661	0.0250345	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571016	CTGGCGCCTGTGCAG[C/T]GCAAGATCGAGGCTC	3993
rs75065631	snp	A/C	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75527167	AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA	3993
rs75087908	snp	C/T	0.152001	0.229992	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575500	TCAGAAGAAGGACAC[C/T]CACAATATCTCAGAC	3993
rs75173279	snp	C/T	6.65203e-05	0.00576678	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568646	CTGAAGCTGTGGGAG[C/T]GGATCATTGCCGCCG	3993
rs75202808	snp	A/G	0.150667	0.229419	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566510	AGACTGTTGCTATAA[A/G]GGGCTGGGTGGCTTT	3993
rs75278200	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567964	AGAAAAAAAAAAAAA[A/G]AGACAAATGGTTTAA	3993
rs75405906	snp	A/G	0	0	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567949	CCCTGTCTCGAGAAA[A/G]GAAAAAAAAAAAAAA	3993
rs75462570	snp	G/T	0.152001	0.229992	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567928	CCTGGGCGACAGAGT[G/T]TGAAACCCTGTCTCG	3993
rs75515900	snp	C/T	0.151334	0.229706	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75575074	CCTTCCCGGGCCTCG[C/T]CTGTCTGGGTCCTTT	3993
rs75557226	snp	G/T	0.0785177	0.181917	intron-variant	LLGL2	GRCh38.p7	17:75547300	TCCAGTTCACCGAGG[G/T]CTATGTGCCAGGCAT	3993
rs75779916	snp	C/T	0.332106	0.236133	intron-variant	LLGL2	GRCh38.p7	17:75548268	TTTACAGAAGGACAA[C/T]TTTTTTTTTCCTTTT	3993
rs75864371	snp	A/G	0.151334	0.229706	intron-variant	LLGL2	GRCh38.p7	17:75574733	GGGAGGAAGAGCCCC[A/G]GCCCCACTCCCCTGG	3993
rs75902792	snp	A/G	0.0770498	0.180522	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542408	CCCATCCTGCTGGGA[A/G]TGGACGGAGCTGTGC	3993
rs75909267	snp	C/T	0.12284	0.215245	intron-variant	LLGL2	GRCh38.p7	17:75574834	GGCACCCCGTCCTGC[C/T]CAGGGTGATCTTGAG	3993
rs75949452	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75561213	TTTAGTCTCATAACT[C/G]TCTCTGAGAAGTCTC	3993
rs75998331	snp	C/T	0.0510075	0.151334	intron-variant	LLGL2	GRCh38.p7	17:75573305	GGGCTGGGTGGGTGT[C/T]GGGGCCCCGGGCACT	3993
rs76009036	snp	A/C	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75561922	GCGAGACTCCCATCT[A/C]AAAAAAAAAAAATTA	3993
rs76052617	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75557373	GGGACAGTCCTTCCC[C/T]GGCCTGAGGCTGGAT	3993
rs76242740	snp	C/T	0.157311	0.232183	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567129	CCTGGGAGCAGCCAG[C/T]GGGCAGCAGACCCCA	3993
rs76451180	snp	C/T	0.0126979	0.078662	intron-variant	LLGL2	GRCh38.p7	17:75535303	CTTCTTAATCAGCAG[C/T]GGGCTGTGGGGAGCA	3993
rs76468692	snp	C/T	0.0652144	0.168387	intron-variant	LLGL2	GRCh38.p7	17:75532911	GAACCCTGTGGGGTC[C/T]TACCTCAGTGTTTCG	3993
rs76502707	snp	A/G	0.00755907	0.0610114	intron-variant	LLGL2	GRCh38.p7	17:75538300	TCCCTGCCTAGGACA[A/G]CTCAGGAGGCCCACT	3993
rs76504264	snp	C/G	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566170	AGGTAGGGGCGAAGA[C/G]AGGGCAGAATGGCCC	3993
rs76507861	snp	C/T	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566546	CCACAGCTACTCAGC[C/T]TAATGCCATTGCAGA	3993
rs76521010	snp	C/T	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541547	CAGCAAAGTGGGATC[C/T]CCACCTCTGGTCTGA	3993
rs76567711	snp	C/T	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75563624	TCTTGGGGAACTTCT[C/T]GGAGCAAGATTCCCA	3993
rs76593171	snp	G/T	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75553265	GGCTATCCCATTTAG[G/T]TATGACCATTTGCAG	3993
rs76714728	snp	A/G	0.153	0.230415	intron-variant	LLGL2	GRCh38.p7	17:75573762	CCCTCCCAGGCTCCG[A/G]CTCTCCTTGCCTCTT	3993
rs76794203	snp	A/G	0.0140947	0.0827569	intron-variant	LLGL2	GRCh38.p7	17:75562982	TTCCCCCTGGTGGAC[A/G]GCATCGGAGGCTCAC	3993
rs77041846	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75548272	CAGAAGGACAATTTT[C/T]TTTTTCCTTTTTTTT	3993
rs77046948	snp	C/G	0.152001	0.229992	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575570	GCTGCTGAAGCGGGG[C/G]TGGTACCCAAGGAGA	3993
rs77073190	in-del	-/A	0.999623	0.00267651	intron-variant	LLGL2	GRCh38.p7	17:75555871	GAGTCACAAAGGGAC[-/A]GGGGGTGGGGCCTGG	3993
rs77329984	snp	C/G	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75531617	TGTTTTCCTCTGTCA[C/G]GAGCAGTTTGCAGAG	3993
rs77340657	snp	C/T	0.0520411	0.152686	intron-variant	LLGL2	GRCh38.p7	17:75563282	AGGCGATGGGAACGC[C/T]GCCTCGGTCCAGCGT	3993
rs77422917	snp	A/C	0.314057	0.241654	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525518	GCGGAACCCCGAGGC[A/C]GTTCGCGAGGCCCCG	3993
rs77637305	snp	A/G	0.140334	0.224663	intron-variant	LLGL2	GRCh38.p7	17:75568887	CAGTAGGATATGTGG[A/G]GTGGGAGCAGAGCCC	3993
rs77666414	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75561215	TAGTCTCATAACTGT[C/G]TCTGAGAAGTCTCTG	3993
rs77672090	snp	A/T	0.151668	0.229849	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575493	CCTACTGTCAGAAGA[A/T]GGACACCCACAATAT	3993
rs77726315	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75540716	AGTCCGAGTTCTGCC[G/T]CTTCCTACTTGGTGA	3993
rs77747675	snp	G/T	0.152001	0.229992	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575623	CTGGGTTATTTAGAT[G/T]GGACATGGGCTGGAT	3993
rs77828821	snp	G/T	0.151334	0.229706	intron-variant	LLGL2	GRCh38.p7	17:75574807	ATGTCTGGGCTCAGC[G/T]TGGGCGGCTGGGGCA	3993
rs77862005	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75555651	ACCAAGATTTTCTCC[C/T]GAGAGACCGGTGTCT	3993
rs77865803	snp	A/G	0.0158469	0.0875917	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542044	CGATTTTGTAAAATC[A/G]GGTCACCCTCCCAGC	3993
rs77906790	snp	A/G	0.157311	0.232183	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567280	ACTAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC	3993
rs77912916	snp	A/C	0.5	0	downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564862	AGCCAGACTGTGTCT[A/C]AAAAAAAAAAAAAAA	3993
rs77958196	snp	C/G	0.0669477	0.17027	intron-variant	LLGL2	GRCh38.p7	17:75558105	CTGGCACTCAAGGCA[C/G]GCAGGGGATGGTGTC	3993
rs78062176	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558886	CTCCATCCGCACCCC[A/G]CCTCCTCCATCCACA	3993
rs78153446	in-del	-/CAAACAAA			intron-variant	LLGL2	GRCh38.p7	17:75528758	AAACAAACAAACAAA[-/CAAACAAA]AAATGGCCCATAATC	3993
rs78270542	snp	A/C	0.105214	0.203807	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575709	CCGGTGTCTGAGACA[A/C]CTGTGGTTCCTGCCA	3993
rs78329331	snp	C/G	0.0517044	0.152246	intron-variant	LLGL2	GRCh38.p7	17:75554023	AAAGTCATTTTAGGC[C/G]GGGTATGATGGCTCA	3993
rs78343781	snp	A/C	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75562428	GCTCCCTCTTGCCCC[A/C]ACATTGACTTTTCCA	3993
rs78367086	snp	C/T	0.00399958	0.0445398	missense, intron-variant	LLGL2	GRCh38.p7	17:75564520	CCAGTAGGAGAGCTT[C/T]GGGAGTGGGTGCCCA	3993
rs78407425	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567966	AAAAAAAAAAAAAAA[A/G]ACAAATGGTTTAATC	3993
rs78576115	snp	A/T	0.0295035	0.117819	intron-variant	LLGL2	GRCh38.p7	17:75559606	GGTTAGCATCATAGC[A/T]CTAAAAAGGGGGCTT	3993
rs78892944	snp	C/T			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567934	CGACAGAGTGTGAAA[C/T]CCTGTCTCGAGAAAA	3993
rs78932281	snp	C/T	0.0162398	0.0886349	intron-variant	LLGL2	GRCh38.p7	17:75551754	CGAGGCCAATGGGAA[C/T]ATAATATGAGCCATG	3993
rs78946558	in-del	-/ACGCCGAGG			utr-variant-5-prime, intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75525795	CGAGGGACGCCGAGG[-/ACGCCGAGG]CCTCGGGCGGGGGCT	3993
rs79223978	snp	C/G	0.152001	0.229992	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575565	GGGGTGCTGCTGAAG[C/G]GGGGCTGGTACCCAA	3993
rs79315745	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75560163	TGATGAAGCAGGGCC[C/T]GTCTGCCCAGGGCAG	3993
rs79518844	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538643	ATTCCACAGGTAATC[A/G]ACAAGATTAATAAGT	3993
rs79727188	in-del	-/TTT			intron-variant	LLGL2	GRCh38.p7	17:75555291	GGGTAATTTTTGTTC[-/TTT]TTTTTTTTTTTTTTG	3993
rs79878336	snp	A/C	0.5	0	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525191	TGGGCGCCCCCCCGC[A/C]CCCCCCCCCGAGGAA	3993
rs79935209	snp	C/T	0.151334	0.229706	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575273	ATGGAAAGTGGGAGC[C/T]GGTACCCTGCCTGTC	3993
rs80037708	snp	C/T	0.13498	0.22197	intron-variant	LLGL2	GRCh38.p7	17:75569368	CTGGGGAGGAGTGGT[C/T]GATGACTGGGGACAG	3993
rs80250996	snp	A/G	0.0168055	0.0901129	intron-variant	LLGL2	GRCh38.p7	17:75548876	GATCCCTAAGGGAGT[A/G]TAATTGCTTCAAACG	3993
rs80282125	snp	C/G/T			intron-variant	LLGL2	GRCh38.p7	17:75527872	GGCTCACTGCAGACT[C/G/T]GACCTCCCAGGCTCA	3993
rs80292880	snp	A/G	0.0535932	0.154675	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568094	TGCTGAAGACCACGC[A/G]TGCTGCTGCCTGTGG	3993
rs80312478	snp	A/G	0.483995	0.0880135	intron-variant	LLGL2	GRCh38.p7	17:75548296	TTTTTTTTTTTTTTT[A/G]GACGGAGTTTAGCTC	3993
rs111233497	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75558923	CTCCTCCATCCGCAC[C/T]CCACCTCCTCCATCC	3993
rs111240935	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75539625	TTTTTTTTTTTTTTT[A/T]TATACAGAATTTCAC	3993
rs111317355	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75547756	GTTGAACCCTGGAGG[C/T]GGAGATTGCAGTGAG	3993
rs111395460	snp	C/T	0.000294913	0.0121396	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524584	ACTGTGACCCTCTCC[C/T]TTCCCTGCTGCCTTG	3993
rs111406685	snp	C/T	0.0372196	0.131242	intron-variant	LLGL2	GRCh38.p7	17:75554270	TCGCACCATTGCACT[C/T]CAGGCTGGGTGACAA	3993
rs111411259	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75558943	CTCCTCCATCCGCAC[C/T]CCGCCTCCTCCATCC	3993
rs111418394	snp	A/G	0.0737376	0.17729	intron-variant	LLGL2	GRCh38.p7	17:75556786	TTTTCGGCACTTTGG[A/G]AGGCTGAGGCGGGCA	3993
rs111422106	snp	A/G	0.00214249	0.0326597	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570959	TTGCAGGCACAGGAG[A/G]GGAGTGCCAAGGCTG	3993
rs111424266	snp	A/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75562944	GCATAGGGAGCCCCA[A/T]GGCTGTGCCATGCTG	3993
rs111488569	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540841	GTGTGAGGGGCTCCA[C/T]GCTCACAAACTCACA	3993
rs111520361	snp	A/G	0.00953873	0.0683987	intron-variant	LLGL2	GRCh38.p7	17:75555405	CTTAAACATCTTTAT[A/G]CCTCCCAGGTTTTTC	3993
rs111582509	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558899	CCACCTCCTCCATCC[A/G]CACCACGCCTCCTCC	3993
rs111596085	snp	G/T	0.000103429	0.00719052	intron-variant	LLGL2	GRCh38.p7	17:75573905	GGGCTCTCAGAGCCG[G/T]GCAGGGAGCCCGGGG	3993
rs111612060	snp	A/G	0.104504	0.2033	intron-variant	LLGL2	GRCh38.p7	17:75562761	TTTTAGTAGAGACAG[A/G]GTTTTGCCATGTTGG	3993
rs111664758	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530138	GCACTTGGGCCTTTT[G/T]GAAGTGCCTGATGGG	3993
rs111711973	snp	A/C/T	0	0	splice-acceptor-variant, intron-variant	LLGL2	GRCh38.p7	17:75574869	CCCTCTGTGTCCTTC[A/C/T]GCAGAGTGAGTGGCT	3993
rs111804648	in-del	-/A	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75572665	GCGAGATTCCGTCTC[-/A]AAAAAAAAAAAAAAA	3993
rs111815556	snp	C/T	0.00636936	0.0560724	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574362	GAGGCGGGGTACAGA[C/T]CCATGGGCACCCACG	3993
rs111884592	snp	A/C	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558904	TCCTCCATCCACACC[A/C]CGCCTCCTCCATCCG	3993
rs111935252	snp	C/T	0.00914312	0.0669923	intron-variant	LLGL2	GRCh38.p7	17:75555718	CACCCATAAGGCCCC[C/T]ATGCCACTGAGGAGG	3993
rs111939749	snp	C/T	0.375	0.216506	intron-variant	LLGL2	GRCh38.p7	17:75558963	CTCCTCCATCCGCAC[C/T]CCGCCTCCTCCATCC	3993
rs111941746	snp	A/G	0.0372196	0.131242	intron-variant	LLGL2	GRCh38.p7	17:75555221	TCACAAGTGCAGAAG[A/G]CTCGAAGGATGTACA	3993
rs111972085	snp	C/G/T	0.00580751	0.0535762	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524581	GAAACTGTGACCCTC[C/G/T]CCCTTCCCTGCTGCC	3993
rs112017789	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75529500	ATGAGCCACTGCACC[C/T]GGCCCCTGCCAGTCC	3993
rs112024009	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542961	CCCGACTTGGGCTCT[A/G]ATCTGGGAAGGATGG	3993
rs112041303	snp	C/G/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567478	TCAAAAAATAAAAAA[C/G/T]AAAAACAAAAATTAG	3993
rs112047184	snp	A/C	0.00207743	0.0321621	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573077	GCCCTGGAGGGCTCA[A/C]GAGTGCGGCGGGTCA	3993
rs112088801	snp	A/G	0.109814	0.206997	intron-variant	LLGL2	GRCh38.p7	17:75572430	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC	3993
rs112106277	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75546872	GAGGGCAGGTCCAGC[A/G]GACGGTGGGATACCC	3993
rs112112336	snp	A/G	0.437824	0.164991	intron-variant	LLGL2	GRCh38.p7	17:75558846	CTCCATCCGCACCCC[A/G]CCTCCTCCATCCGCA	3993
rs112123203	snp	A/G	0.0314385	0.121371	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566799	GCTCAGCTGGGCGGG[A/G]ATCAAGTCTGAGGAC	3993
rs112142185	in-del	-/AGG	0.5	0	intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523085	TCAGGAGGCTGAGAC[-/AGG]AGAATTGCTTGAACC	3993
rs112192911	snp	C/G	0	0	missense, intron-variant, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574871	CTCTGTGTCCTTCAG[C/G]AGAGTGAGTGGCTGA	3993
rs112224435	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75558825	CCTCCATCCACACCA[C/T]GCCTCCTCCATCCGC	3993
rs112258196	snp	G/T	0.0236746	0.106192	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541860	TTAGCCTTCCAAGTA[G/T]CTGGGATTACAGGCG	3993
rs112307097	snp	C/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75572253	GGACAGGGGGCCAGG[C/T]GCGGTGACTCATGCC	3993
rs112366094	snp	A/C	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524169	GTCAGAATTCTTGCA[A/C]CCCAACTCCTTCCGT	3993
rs112375011	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75529325	CCTCAGCATCCTGAG[G/T]AGCTGGGATTGCAGG	3993
rs112381847	in-del	-/TTTT	0	0	intron-variant	LLGL2	GRCh38.p7	17:75548280	CAATTTTTTTTTTCC[-/TTTT]TTTTTTTTTTTTGGA	3993
rs112393371	snp	A/G	0.0308092	0.120231	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573620	CCCCAAGAAGGCCCC[A/G]AGCCGAGCCAGGTGA	3993
rs112423278	snp	A/G	0.316485	0.240998	intron-variant	LLGL2	GRCh38.p7	17:75529346	GGATTGCAGGCAGGC[A/G]CCACCAGGCCCAGCT	3993
rs112454420	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75544894	CTCGCTTTTGGGCCT[C/T]GGGATATGGGGGTGC	3993
rs112456263	snp	A/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75546830	AGGTCCAGCAGACAG[A/G]CGGAGGGCAGGTCCA	3993
rs112504413	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75552618	TGTATTTTACACTTA[C/T]GGCACATCTCAGTTC	3993
rs112545319	snp	C/G	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75547119	CACCTTTTGGCTCAA[C/G]TCCTTTATACCCACA	3993
rs112556755	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75533128	CCTCAGCCTCCCGAG[G/T]AGCTGGGACTACAGG	3993
rs112563171	snp	A/G	0.00212576	0.0325325	intron-variant	LLGL2	GRCh38.p7	17:75559210	CATGGCATCTCCCCT[A/G]CTGGGCAGTGGTCGG	3993
rs112639131	snp	C/T	0.0154538	0.0865337	intron-variant	LLGL2	GRCh38.p7	17:75548438	ATGTGCCACCACGCC[C/T]GGCTAAAGGACAGCT	3993
rs112645203	snp	A/G			splice-donor-variant	LLGL2	GRCh38.p7	17:75543502	TTCCAGTTTAACAAG[A/G]TAAGTTAGGGAGAGC	3993
rs112724865	snp	C/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75555873	GTCACAAAGGGACAG[C/G]GGGTGGGGCCTGGTA	3993
rs112730714	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75546806	AGGTCCAGCAGACAG[A/G]CGGAGGGCAGGTCCA	3993
rs112737044	snp	A/G	0.385359	0.210185	intron-variant	LLGL2	GRCh38.p7	17:75558839	ACGCCTCCTCCATCC[A/G]CACCCCACCTCCTCC	3993
rs112746573	in-del	-/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75557887	GCCTGACAGTTGCCA[-/G]GGTAGGGCTTCGCCT	3993
rs112753782	snp	A/G	0.00418479	0.0455509	intron-variant	LLGL2	GRCh38.p7	17:75574061	GGAGGGAAGGGTCCC[A/G]AGTGAGCAGGTAGTG	3993
rs112820207	snp	A/C	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75533627	TATTTTCTGATGCCT[A/C]TTGTGTGGTTCTAGA	3993
rs112824868	snp	A/G			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564879	AAAAAAAAAAAAAAA[A/G]GGGCTCTGCACAGAT	3993
rs112833709	snp	C/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75572121	GACATCCAGGAGGCT[C/T]GGACCTTGGGCAAAA	3993
rs112983066	snp	C/G/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75555312	TTTTTTTTTTTGAGA[C/G/T]GGAGTCTCGCTCTGT	3993
rs112997778	snp	C/T	0.0310518	0.120672	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566597	CACAAGGGGCGTATC[C/T]GTGTTCCAGGACAGC	3993
rs113078415	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75551714	TTCTCTGTGGCCTGA[C/T]GTTCCTGCTGGTGTG	3993
rs113135610	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528170	ACCCAGGCTGGAGTG[C/T]AGTGGCGAGATCTCG	3993
rs113200131	snp	C/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75527950	GCAGCACCATGCACA[C/G]CTAATTTTCTATTTT	3993
rs113251399	snp	C/T	0	0	intron-variant	LLGL2	GRCh38.p7	17:75548819	GGTCTCCTACAGTGG[C/T]ATTTTGGGGTGGTAT	3993
rs113252202	snp	A/G	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75546349	CCGACTGCCCGGCTC[A/G]CCAGCTGTGTGACCT	3993
rs113365742	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566344	TGTGGGGGACACGGA[A/G]TGGAGCAAAGACGGG	3993
rs113401352	snp	A/G	0.00202359	0.0317443	intron-variant	LLGL2	GRCh38.p7	17:75573306	GGCTGGGTGGGTGTC[A/G]GGGCCCCGGGCACTG	3993
rs113492706	snp	A/C/G	0.0583635	0.160908	intron-variant	LLGL2	GRCh38.p7	17:75573669	TCTCCCGCCCCTCCC[A/C/G]CCCCTCCCTGCCCTC	3993
rs113514116	snp	C/T	0.178785	0.239642	intron-variant	LLGL2	GRCh38.p7	17:75558998	CCCGCCTCCTCCATC[C/T]GCACCCCGCCTCCTC	3993
rs113546676	snp	G/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567235	TTGGGAGGCCAAGGA[G/T]GGCAGATCACCTGAG	3993
rs113576696	snp	A/G	0.0376037	0.131863	intron-variant	LLGL2	GRCh38.p7	17:75555965	GCTTCCTGCTGGGTC[A/G]TCTGGTGCTGCAGCT	3993
rs113599872	snp	A/G	0.0368353	0.130617	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542357	CCCTGCCTGGAGCAC[A/G]CGCCTCCAGGGTGCG	3993
rs113665966	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75559249	CAGCTGTTCTTGTCA[A/C]AGGGCTGCCCCCAGT	3993
rs113694762	snp	C/T	0.5	0	intron-variant	LLGL2	GRCh38.p7	17:75553426	TCCTTGTGAGAGCCA[C/T]TGGACTAGACTGACT	3993
rs113725132	snp	A/C	0.460027	0.135605	intron-variant	LLGL2	GRCh38.p7	17:75550803	AAAAAAAAAAAAAAA[A/C]ACACACACACACAAA	3993
rs113725313	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75558926	CTCCATCCGCACCCC[A/G]CCTCCTCCATCCGCA	3993
rs113838087	snp	A/G	0.178144	0.239451	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525168	CCCTCCGGCCGACAC[A/G]GAGGAGGTGGGCGCC	3993
rs113998041	snp	A/C	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75557789	GCTGTTGGTGATAGG[A/C]CCCCTGGGGTGCCGT	3993
rs114228216	snp	G/T	0.0111196	0.0737302	intron-variant	LLGL2	GRCh38.p7	17:75570800	CCAAGGGCACCTCCC[G/T]CTTGGACAAGGGTCC	3993
rs114250197	snp	C/G/T	0.0360663	0.129354	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542209	CACCTCCCAAGAACG[C/G/T]GAAATCCTTCAAACC	3993
rs114272373	snp	C/T	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75553427	CCTTGTGAGAGCCAT[C/T]GGACTAGACTGACTG	3993
rs114278352	snp	C/T	0.00600564	0.0544679	intron-variant	LLGL2	GRCh38.p7	17:75558052	GGGGAGGGCAGCCCC[C/T]CTCTGTGTTTGCATC	3993
rs114364914	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75555595	AGGGCAGGGCCTCCG[C/T]GGTACTCTAGGCCCC	3993
rs114480869	snp	C/T	0.00755907	0.0610114	intron-variant	LLGL2	GRCh38.p7	17:75540634	ATTGCAAGGGTGTCA[C/T]TGGGCATCCTTTGTT	3993
rs114487761	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566308	CTAGCCTCTGCTCCA[A/G]AAGGATCTGTCTGGC	3993
rs114498260	snp	C/T	0.029116	0.117091	intron-variant	LLGL2	GRCh38.p7	17:75560411	CCTGTAGTTAGCTGG[C/T]GGGAATCTAGTCGGC	3993
rs114513045	snp	C/T	0.00138934	0.02632	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569027	TCGGGTGTCTGCCTG[C/T]GGCTGCTCTACAAAC	3993
rs114524736	snp	C/G	0.0126979	0.078662	intron-variant	LLGL2	GRCh38.p7	17:75552753	GTTCTTCTAGAACCC[C/G]AGTTGTTCCAGACAT	3993
rs114560384	snp	C/T	0.0182019	0.0936463	intron-variant	LLGL2	GRCh38.p7	17:75534678	CTGAGACAAGGTCTC[C/T]CTAAGTTGCCCAGGC	3993
rs114699441	snp	A/G	0.0614824	0.164198	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541660	TGGTTCCTGGTATTC[A/G]GTTTTGAGATAACTG	3993
rs114747014	snp	A/G/T	0.0207125	0.0999761	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563412	TACTGCCAGTGGCCC[A/G/T]TGTCCAGCGAAGCCC	3993
rs114781240	snp	G/T	0.0158469	0.0875917	intron-variant	LLGL2	GRCh38.p7	17:75573336	GCACGGACGGGAAGG[G/T]TGGCCAGGGGTGTTG	3993
rs114832677	snp	C/T	0.0121997	0.0771429	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569083	CGACACGGACCCCAA[C/T]GAGAACTTCAGTGCC	3993
rs114836961	snp	C/G	0.0785177	0.181917	intron-variant	LLGL2	GRCh38.p7	17:75547250	TTGCGAACAGTCTCT[C/G]AACTCTGCCAGGAAC	3993
rs114845805	snp	A/G	0.00914312	0.0669923	intron-variant	LLGL2	GRCh38.p7	17:75561792	CCTGGCATGGTTGTG[A/G]GTGCCTGTAATCCCT	3993
rs115026154	snp	C/G	0.0107065	0.0723784	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570013	GCAGGCTGTGGAGCA[C/G]GTGGAGGCCGACCTG	3993
rs115064277	snp	C/G	0.0599851	0.162463	intron-variant	LLGL2	GRCh38.p7	17:75547541	GAATTAAATTGACGA[C/G]AGGCGGGGCGCAGTG	3993
rs115113002	snp	G/T	0.00223146	0.0333279	intron-variant	LLGL2	GRCh38.p7	17:75571134	GTTGGGGGGCAGGGG[G/T]TAGTGGGCAGCAGAC	3993
rs115163832	snp	C/G	0.00597247	0.0543191	intron-variant	LLGL2	GRCh38.p7	17:75559717	GGTTTCAGAACCCCA[C/G]GGGCTCCGCAGCGGG	3993
rs115174824	snp	A/G	0.0146672	0.084371	intron-variant	LLGL2	GRCh38.p7	17:75549965	TGCTCTCCTTTCCCA[A/G]CCCCCCTGTCAAAAG	3993
rs115360458	snp	C/T	0.0174175	0.0916809	intron-variant	LLGL2	GRCh38.p7	17:75560709	CAAACTAGTCTCGAA[C/T]TCCCGACCTCAGGTG	3993
rs115379287	snp	A/T	0.0637235	0.166737	intron-variant	LLGL2	GRCh38.p7	17:75550715	GAGCCCGGGAGGAGG[A/T]GGTTACAGTGAGCTG	3993
rs115396309	snp	A/G	0.0281633	0.115276	intron-variant	LLGL2	GRCh38.p7	17:75546222	CAGGCCAGGAGTGGC[A/G]AAGAACAGATTTGAG	3993
rs115417974	snp	C/G	0.0314385	0.121371	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543282	AAGCTGGCCTGGCCC[C/G]GGGGTGGCAGCCTAC	3993
rs115583163	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75552230	TCATACCTGTAATCC[C/T]AGCACTCTGGCACTC	3993
rs115615615	snp	A/C/G/T	0.0121523	0.0770266	intron-variant	LLGL2	GRCh38.p7	17:75570343	CAGCCTGCCATCCCC[A/C/G/T]CAAGGTGCACACTGC	3993
rs115681901	snp	C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75547142	TACCCACACCAAGCC[C/T]GATGCCTCAAAGAGA	3993
rs115787695	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75563958	GGGAGACAGGGTAGA[C/T]GCTATTCACGTCTCT	3993
rs115961177	snp	A/G	0.0325976	0.123435	intron-variant	LLGL2	GRCh38.p7	17:75534339	GTTGTGATTCCATAG[A/G]ATAGATGGTGGGGGG	3993
rs115974525	snp	C/G	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75561597	CTACCCTCCAGCCTG[C/G]GTGACAGAATGAGAT	3993
rs116192373	snp	C/T	0.0123036	0.0774623	intron-variant	LLGL2	GRCh38.p7	17:75569674	CAGGCATTTGTGGCT[C/T]GTGCCTGTAATCCCA	3993
rs116207549	snp	A/T	0.0486741	0.148216	intron-variant	LLGL2	GRCh38.p7	17:75557815	GCCGTGTGTTTTTTC[A/T]CAGGTGCTACCAAGC	3993
rs116220247	snp	C/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75554579	GAACCGAAATCATGC[C/T]GTAGCACCCAGCCTG	3993
rs116275079	snp	C/T	0.0307309	0.120088	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571950	GGGCATCCTGGTGCT[C/T]GACGGACACAGCGTA	3993
rs116293487	snp	C/T	0.0429648	0.14013	intron-variant	LLGL2	GRCh38.p7	17:75546468	ATCGAAGGCCACGTC[C/T]GGCTGGCGGCTGCAG	3993
rs116294831	snp	C/T	0.0105977	0.0720176	intron-variant	LLGL2	GRCh38.p7	17:75563284	GCGATGGGAACGCCG[C/T]CTCGGTCCAGCGTGC	3993
rs116357873	snp	C/T	0.030278	0.119257	intron-variant	LLGL2	GRCh38.p7	17:75547538	TATGAATTAAATTGA[C/T]GAGAGGCGGGGCGCA	3993
rs116376623	snp	A/G	0.0599851	0.162463	intron-variant	LLGL2	GRCh38.p7	17:75548984	TGCTTCCATTCTGCA[A/G]GGGAGGAGACTAAGG	3993
rs116429274	snp	A/G	0.135825	0.222405	intron-variant	LLGL2	GRCh38.p7	17:75529236	GAAGTCTCCTCTGTC[A/G]CCCAGGATGGAGCAC	3993
rs116432680	snp	A/G	0.0414363	0.137845	intron-variant	LLGL2	GRCh38.p7	17:75546435	GTTGGTGTGAGGACT[A/G]CATGAGTTCCTGCAC	3993
rs116513256	snp	A/G	0.0810805	0.184299	intron-variant	LLGL2	GRCh38.p7	17:75561493	TTAGTTGGGCAAGGC[A/G]GCACACGTCTGCAGT	3993
rs116584891	snp	A/G	0.000840174	0.0204788	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573257	GGCATCGCCTCCTGC[A/G]TCTTCACCAAATATG	3993
rs116679012	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548223	CCTGTACTTGACTAA[C/T]GTAGCTTTCCTTTGT	3993
rs116761409	snp	C/T	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75552849	GGTGGCCCCATGGGG[C/T]TCATGGCTACCGTTC	3993
rs116774033	snp	A/G	0.029116	0.117091	downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75565049	TGCCCCGGGCTCTCT[A/G]CCCTTTCCAGACTGT	3993
rs116833026	snp	A/C	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75556341	ACCTGGGCATGAGTG[A/C]ATCCCTGGTGGGATG	3993
rs116880598	snp	A/T	0.0475351	0.146656	intron-variant	LLGL2	GRCh38.p7	17:75536578	CCGGAACATTCCACC[A/T]GCAGGACAGGGCTGG	3993
rs116884397	snp	A/G	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75531581	CCTGGGGCGAGGCAC[A/G]CCAGGTCTGCTTGGC	3993
rs116971898	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75530894	AGCAGTGGAGGGCGC[A/G]GCTTCTCCTAAATGG	3993
rs116984828	snp	A/G	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75532866	TGGCCTTGGCCGGAG[A/G]CTTGAGGACAGGGTA	3993
rs117023929	snp	C/T	0.0146672	0.084371	intron-variant	LLGL2	GRCh38.p7	17:75527529	TATATTAAAATGACA[C/T]TACATTCATAAATAA	3993
rs117031010	snp	A/G	0.0271869	0.113447	intron-variant	LLGL2	GRCh38.p7	17:75536132	ACAGGCAGGAGTGGA[A/G]ACTGAGGTTGGATGG	3993
rs117066674	snp	G/T	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75564211	TCCAAGTCCTCCTGG[G/T]CTGTAGCAGTTGGAA	3993
rs117175545	snp	A/C	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75530078	GGGTGGACTCAACTT[A/C]CATGAAGCATAAGAG	3993
rs117249958	snp	C/G	0.0603597	0.1629	intron-variant	LLGL2	GRCh38.p7	17:75537969	TGCCCGTCACCATAC[C/G]TGGCTAATTTTTTGT	3993
rs117314167	snp	C/T	0.0429648	0.14013	intron-variant	LLGL2	GRCh38.p7	17:75552229	CTCATACCTGTAATC[C/T]CAGCACTCTGGCACT	3993
rs117416681	snp	A/G	0.0678174	0.1712	intron-variant	LLGL2	GRCh38.p7	17:75529898	TAAAAAAAGATTTTT[A/G]GTGTCTTTCTAGGCT	3993
rs117442223	snp	C/T	0.0535932	0.154675	intron-variant	LLGL2	GRCh38.p7	17:75550941	CTTCTGTTAGCTGCT[C/T]TTAGTCCTGTTCCCA	3993
rs117605759	snp	C/T	0.0554779	0.157039	intron-variant	LLGL2	GRCh38.p7	17:75550971	AAATCCCAATCCCTT[C/T]CCTGTTCCCAACAAG	3993
rs117643138	snp	A/G	0.0256215	0.110247	intron-variant	LLGL2	GRCh38.p7	17:75527562	AATAAAATAGAAAAA[A/G]GTAACTTTTTTCTCT	3993
rs117651797	snp	C/T	0.0217236	0.101931	intron-variant	LLGL2	GRCh38.p7	17:75573430	CCCCAGGTGGGGAGG[C/T]AGCCTTGGCAGCCGC	3993
rs117693674	snp	A/G	0.0670745	0.170406	intron-variant	LLGL2	GRCh38.p7	17:75530680	AATTAGCTGGGCATC[A/G]TGGTGTGCACCTGTT	3993
rs117707230	snp	A/G	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75537213	ATTTAGGTTGCTTCT[A/G]ATTTTTTCTGACAGC	3993
rs117715760	snp	C/T	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75528569	CATGGAGATACCCTG[C/T]CTCTATTAAACATAT	3993
rs117791805	snp	G/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75537188	CTTCACCCATCCCCT[G/T]TTGTGGGCCATTTAG	3993
rs117892515	snp	A/G	0.0528381	0.153711	intron-variant	LLGL2	GRCh38.p7	17:75529944	ACTCGTTCTTTGCCG[A/G]GTCCTTGCTGTGTGA	3993
rs118079525	snp	C/T	0.0501905	0.150254	intron-variant	LLGL2	GRCh38.p7	17:75557130	GCAACTCTCTCGCCT[C/T]GGCCTCTCAAAATGC	3993
rs137856107	snp	A/G	0.0444908	0.142359	intron-variant	LLGL2	GRCh38.p7	17:75549449	GCCTTCCCTGCCCGT[A/G]CCCACCCTCCTCTGT	3993
rs138009663	snp	C/T	0.00676609	0.0577691	intron-variant	LLGL2	GRCh38.p7	17:75553758	AACTGAACTAAAAAC[C/T]TTCCTGAAGATGGTT	3993
rs138051975	snp	C/T	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75527405	GACTGGGCCCATCTT[C/T]GTGGGGGCTCCTGGA	3993
rs138058959	in-del	-/G			intron-variant	LLGL2	GRCh38.p7	17:75526642	GGCGCCCCTTCCCCT[-/G]GGGGATCCGTATGCG	3993
rs138074005	snp	C/T	5.00739e-05	0.00500344	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559364	CAGCTGCCAGCTTTT[C/T]GTGCGCTGGAGGACC	3993
rs138134053	snp	C/T	0.00716477	0.0594227	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556047	GCTTCTCGTTGCAGA[C/T]GGTGGAGCATGGCTT	3993
rs138160129	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75538680	TTCAGTGTGTCCAAA[C/T]GTGGCCAGGTCCAAG	3993
rs138247812	snp	C/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75562116	TGGCTGTTGGTCCTG[C/T]GCCTGCTGCCTTGTG	3993
rs138298902	snp	C/G	0.046775	0.145601	intron-variant	LLGL2	GRCh38.p7	17:75530800	TGGGTGACAGAGTGA[C/G]ACTCTAACTCAAAAA	3993
rs138323474	in-del	-/C	0.0554779	0.157039	intron-variant	LLGL2	GRCh38.p7	17:75548178	TAAAACCCTCTATTC[-/C]GCAATCATTTTAGAT	3993
rs138337516	snp	A/C	0.311369	0.242351	intron-variant	LLGL2	GRCh38.p7	17:75528178	TGGAGTGCAGTGGCG[A/C]GATCTCGGCTCACTG	3993
rs138338777	snp	A/G	8.41545e-05	0.00648615	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571079	CGGACCCTGTACTTT[A/G]CTGACACCTACCTGA	3993
rs138347449	in-del	-/C	0.0962929	0.197165	intron-variant	LLGL2	GRCh38.p7	17:75527051	GCGTGCACCTGTAGT[-/C]CCAGCTACTCAGGAG	3993
rs138380642	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546259	TAATGTATTTTGATC[A/G]TTTTGATTTGGACAC	3993
rs138434820	snp	A/T	0.0178098	0.0926698	intron-variant	LLGL2	GRCh38.p7	17:75543867	GGAGATGAAAGGATG[A/T]ACTCTTCAGGGGGTG	3993
rs138529634	snp	A/G	0.0588605	0.161139	intron-variant	LLGL2	GRCh38.p7	17:75534701	GCCCAGGCTGGTCTC[A/G]AACTCCTAGGTTCAG	3993
rs138560086	snp	C/T	0.00236006	0.0342704	upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523717	TGTTTACCAGGCCGA[C/T]GCTGTGGCCACATTC	3993
rs138605682	snp	A/G	0.00597247	0.0543191	intron-variant	LLGL2	GRCh38.p7	17:75533578	CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACC	3993
rs138682028	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75553662	GACATAGCATCGCTT[C/T]GTGCTGTTCTCACCT	3993
rs138748466	snp	C/T	8.53148e-05	0.0065307	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559392	ACCGGACCATCAGCT[C/T]GGACGCGGTGCTGCA	3993
rs138752407	snp	C/T	4.9938e-05	0.00499665	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564442	ACGATGGCCAGCAGA[C/T]GGCCTTCGACTTCAC	3993
rs138768921	snp	A/G	1.67818e-05	0.00289665	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564389	GGGTGGCATGCCACG[A/G]GCCAGCTACGGGGAC	3993
rs138851023	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75557481	AAACCGGATCAGGTT[C/G]GGCACCCCGCCAGTC	3993
rs138872671	in-del	-/T	0.318415	0.240457	intron-variant	LLGL2	GRCh38.p7	17:75527776	CCAGCTGTTAGTAAC[-/T]TTTTTTTTTTTCTTT	3993
rs138912319	snp	A/C/G	0.000178926	0.00945707	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570051	ACCAAGAGGGCTACC[A/C/G]CTGGAAGGGGCACGA	3993
rs138915092	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551011	GCTTCTCATAACTAA[C/T]CTAGGGCTCCCCTGC	3993
rs138922188	snp	C/T	0.00120773	0.024544	intron-variant, utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574196	CGGGGCGCCCTGACC[C/T]GGCCTCTACCTTCCA	3993
rs138940243	snp	A/G	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543216	GCCCTGAGGTGGGCC[A/G]GCCTCTAGATCTGAG	3993
rs138948628	in-del	-/GTC	0.246485	0.249975	intron-variant	LLGL2	GRCh38.p7	17:75539456	ATGTTGCCCAGGCTG[-/GTC]GTCTCCAGCTCCTAG	3993
rs138986374	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75534006	CTTCTTGGGACAGCT[A/G]TTCCAGTTTTAGGGC	3993
rs139000321	snp	A/G	0.000320456	0.0126541	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573210	TCAAGCCCCAGGTGC[A/G]CTACAGCTGCATCCG	3993
rs139051456	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567074	CGGGCACCCTCAAGC[C/T]TTGGAGGCATGAAGT	3993
rs139059660	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75531007	CTGTGGTGGGGATGT[C/T]GGAGAGTGCAGGATT	3993
rs139094573	snp	C/G	0.000137608	0.00829369	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573243	GGGAGGACGTCAGTG[C/G]CATCGCCTCCTGCGT	3993
rs139184842	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75540066	CCCCCTTTACAGAGG[A/C]GCTGTCTCTGGAGGC	3993
rs139250953	snp	A/G	0.0126979	0.078662	intron-variant	LLGL2	GRCh38.p7	17:75535996	AGACTTGGGTAGAAA[A/G]TGGATGGGAACCAGC	3993
rs139362844	snp	C/T	0.0011891	0.0243544	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563372	GGACGGCCGCCTGCT[C/T]GTCAGCTGTCACTCT	3993
rs139384077	snp	C/T	9.08769e-05	0.00674019	intron-variant	LLGL2	GRCh38.p7	17:75564333	GCCCCAGCCCACTGC[C/T]GCTCCTCTGTGCCTG	3993
rs139471141	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540307	CTGGAGGTGAGGCCC[G/T]CCAGGTCTAGACCAG	3993
rs139597424	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554349	GCTTGCAGTGACTCA[C/T]GCCTGTAATCCCAGC	3993
rs139610735	in-del	-/C			intron-variant	LLGL2	GRCh38.p7	17:75559847	GCTAAAAAGCCTTGA[-/C]CCGCCACAGGCATGT	3993
rs139621348	snp	C/T	0.000247066	0.0111118	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523276	CTGTGTCCTTGTAGC[C/T]GTGGTCCTTCAGCAT	3993
rs139646711	snp	A/G	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75551799	TTTCCTAGAAGCTGC[A/G]TTGTATAATTATTTA	3993
rs139665791	snp	A/C	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75572525	AAAAAATTAGTTAGG[A/C]GTGGTGGCGGGCACC	3993
rs139749599	snp	C/T	0.00100677	0.0224137	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558170	CTACGGAGCCCCAGG[C/T]GTGGAGTTCATGGGG	3993
rs139774007	snp	A/C	0.0554779	0.157039	intron-variant	LLGL2	GRCh38.p7	17:75545983	AGATGCCAGTAGCAC[A/C]TACATACACACACAG	3993
rs139853128	snp	C/G	0.0275645	0.114116	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567723	AAGGTGGGAAGATCA[C/G]TTGAGCCCAGGAGTT	3993
rs139886019	snp	A/C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563697	CTGTGCCTGTGGGGA[A/C/G]TGACACTTGTCTGAG	3993
rs139895929	snp	A/G	0.00795532	0.062565	intron-variant	LLGL2	GRCh38.p7	17:75535768	CTTGAGATGGAAGGC[A/G]GGCCAGGGTGTGGAT	3993
rs139947606	snp	A/G	3.34947e-05	0.00409221	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568558	AGCAGGCTGGCCACC[A/G]GTCCAGCTGCCCTAC	3993
rs139957010	snp	G/T	0.00795532	0.062565	intron-variant	LLGL2	GRCh38.p7	17:75552068	CGGGAGGTGGAGGTT[G/T]CAGCGAGCTAAGATC	3993
rs140070555	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524182	CACCCCAACTCCTTC[C/T]GTAGAATCTCTTCTC	3993
rs140092848	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75528465	AAAAAAAGGCCAGGC[A/G]TGGTGGCTTACACCT	3993
rs140150284	snp	C/T	1.69243e-05	0.00290893	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559307	CATTCCTCCTGCGAG[C/T]TGCTCTACCTGGGCA	3993
rs140158421	snp	A/G/T	0.00358779	0.0422022	intron-variant	LLGL2	GRCh38.p7	17:75549335	GCTCACAGCCAGCTC[A/G/T]CTCCCCTCGGCCAAA	3993
rs140195852	snp	C/T	0.00196657	0.0312956	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558211	AGAACAACGCTGTGA[C/T]GCAGATCCACCTCCT	3993
rs140238299	snp	C/T	0.0475351	0.146656	intron-variant	LLGL2	GRCh38.p7	17:75533160	TCCCGCCACCACGCC[C/T]GGCTAATTGTTTGTA	3993
rs140238776	snp	A/C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75558730	CTGTTGCGCCCCTGG[A/C/T]AGTGACTGGCATGCG	3993
rs140242230	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75531673	CGGGCGTCCCCCAGC[A/G]GGGCCACCAGCACTG	3993
rs140325578	snp	A/G	7.95809e-05	0.00630746	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570425	TCAAGAAGTCCTTGC[A/G]TCAGTCATTCCGCCG	3993
rs140392290	in-del	-/CCT	0.0704125	0.17392	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542237	ACCTCAGCTTAGATA[-/CCT]TCTTCTCGAAGGTAT	3993
rs140438443	snp	A/C	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561166	CTCGTCCTCTTGATG[A/C]CACTTATCTAAGTTT	3993
rs140444060	snp	A/G	0.0417477	0.138315	intron-variant	LLGL2	GRCh38.p7	17:75570312	CGCGAGGACTCCCAG[A/G]ACCTAGCAGCACTGA	3993
rs140499680	snp	C/T	0.000118637	0.00770094	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571771	ATGGATGAGCCTGTG[C/T]GGGCAGAGCAGGGTG	3993
rs140513267	snp	A/C	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75545502	GAGCGGGGTAGACTC[A/C]TCCGGCTCGGGGAGT	3993
rs140703061	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75546125	AAGAGGGAGGGGATG[C/G]GGAGGGGAGGCGGGT	3993
rs140799060	snp	C/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75529600	GGGCTCTGTGTCTCA[C/T]GCCTGTAATCCCAGC	3993
rs140802427	snp	G/T	0.0821764	0.185298	intron-variant	LLGL2	GRCh38.p7	17:75560849	AAAGAAAAAACATTT[G/T]TTTTGAGAGAGTCTT	3993
rs140832493	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75565802	GTGGGCACCCTGAAG[C/T]TCTCACGTAATGGTT	3993
rs140870664	snp	A/G	3.48377e-05	0.00417345	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569084	GACACGGACCCCAAC[A/G]AGAACTTCAGTGCCC	3993
rs140904191	snp	C/T	0.0588605	0.161139	intron-variant	LLGL2	GRCh38.p7	17:75533550	ACCTCATGATCTGCC[C/T]GCCTCGGCCTCCCAA	3993
rs140931096	snp	C/G	1.65441e-05	0.00287607	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558213	AACAACGCTGTGACG[C/G]AGATCCACCTCCTGC	3993
rs140939369	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543107	AACCTCAGGGCCCGC[C/T]GGCCCTCCTTGTGCT	3993
rs141041567	snp	C/T	0.000523892	0.0161763	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563462	CAGCCTCGTGCCTTA[C/T]GGTCAGTGTTTCACC	3993
rs141067600	snp	G/T	0.0715223	0.175059	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525405	CCCGGGACCGCAGGC[G/T]TTCCGGGAACTATTT	3993
rs141069900	snp	A/G	0.0011984	0.0244492	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559397	ACCATCAGCTCGGAC[A/G]CGGTGCTGCAGCGGT	3993
rs141145363	snp	G/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75544696	GGAGAGGTGGGTCGT[G/T]GGGTGGAGGGACCTC	3993
rs141206038	snp	A/C	0.0314385	0.121371	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526364	GTCTCCGGCCTTTCT[A/C]CAGCTGGGGCGGCTT	3993
rs141229091	in-del	-/T			intron-variant	LLGL2	GRCh38.p7	17:75560800	CAGTTTGTTTATTTA[-/T]TTAAAAAAAAAAAAA	3993
rs141305094	snp	C/T	0.000168093	0.00916614	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564398	GCCACGGGCCAGCTA[C/T]GGGGACCGCCACTGC	3993
rs141314483	snp	C/T	0.0267878	0.112589	intron-variant	LLGL2	GRCh38.p7	17:75553701	AGGGTCACTATCCCC[C/T]GGGGTGGGAGGCGGG	3993
rs141444394	snp	C/T	0.000436293	0.0147633	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563121	CTACAGCCGAGGCCT[C/T]GTTGTCATCTGGGAC	3993
rs141463111	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75548913	GACACAGGTCGACGC[C/T]TTACCAGGACTTGCC	3993
rs141515395	snp	C/T	5.07181e-05	0.00503552	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571742	CCCTGCGTGTGCCTC[C/T]CGCCGAGCGGAGAAT	3993
rs141534334	snp	C/T	3.40808e-05	0.00412786	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571685	CCCGGCACTGCCCCT[C/T]GCTGTGGGCTGGCAC	3993
rs141562656	in-del	-/AA			intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567951	CTGTCTCGAGAAAAG[-/AA]AAAAAAAAAAAAAAG	3993
rs141595457	snp	C/G	0.000381487	0.0138057	intron-variant	LLGL2	GRCh38.p7	17:75571619	GTTGCCCAGCTCCAC[C/G]CGACTCCCACGCTAA	3993
rs141617348	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542585	GGATTCTATGGTGGG[C/T]GGAGAGTTTAGGGGC	3993
rs141619636	snp	C/T	0.000247727	0.0111266	utr-variant-3-prime, stop-gained, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574901	AGCGTCCAGGCTGCG[C/T]GATGAGCACACACTA	3993
rs141680210	snp	A/G	0.0174175	0.0916809	intron-variant	LLGL2	GRCh38.p7	17:75538103	GGCGTGAGCCACCTC[A/G]CCCAGCCTGGAAGGG	3993
rs141743615	snp	A/G			upstream-variant-2KB, synonymous-codon, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523738	GGCCACATTCCGAAA[A/G]AATAACCCTGGCAAA	3993
rs141769096	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523424	AGTAGGGTGTAAACT[A/T]GAGGACTGTTCCAGG	3993
rs141802283	snp	A/C	0.0737376	0.17729	intron-variant	LLGL2	GRCh38.p7	17:75556779	AAAATTTTTTTCGGC[A/C]CTTTGGGAGGCTGAG	3993
rs141812365	snp	A/T	0.0748431	0.178382	intron-variant	LLGL2	GRCh38.p7	17:75539626	TTTTTTTTTTTTTTT[A/T]ATACAGAATTTCACT	3993
rs141822287	snp	A/G	3.44127e-05	0.00414791	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523766	AAACCCTATGCCCGG[A/G]TGTGCATTAGTGGGT	3993
rs141890823	snp	A/G	0.0138799	0.0821421	intron-variant	LLGL2	GRCh38.p7	17:75526931	CCAGCACTTTGGGAA[A/G]CCAAGGCAGGAGGAT	3993
rs141950888	snp	A/G	0.000461194	0.0151784	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524300	TCTGCAGCCTCAAGC[A/G]GTTGTCTTACCAGAG	3993
rs142036197	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555676	GTGTCTCCATTGTTC[C/T]AAACTCCCCCTACTT	3993
rs142104585	snp	A/G	0.0490535	0.14873	intron-variant	LLGL2	GRCh38.p7	17:75553314	CAAAGGCCAGGCCTG[A/G]GGCACCCCCCGTCTC	3993
rs142158542	snp	C/G	0.0161684	0.0884465	intron-variant	LLGL2	GRCh38.p7	17:75569207	CTGCTCACAGGGCCC[C/G]TCCCCTTCTCCAGGT	3993
rs142162532	snp	A/G	0.0123036	0.0774623	intron-variant	LLGL2	GRCh38.p7	17:75547641	ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCATC	3993
rs142199654	snp	C/G	0.000317696	0.0125995	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574645	ATCGAGCCGCCGTGG[C/G]GTGCAGCCTCAGCAA	3993
rs142232099	snp	A/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75537041	TTGGCCAGGCTGCTC[A/G]CAAACTCCTGACCTC	3993
rs142268975	in-del	-/C	0.0460205	0.144542	upstream-variant-2KB, downstream-variant-500B, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525192	GGGCGCCCCCCCGCA[-/C]CCCCCCCCCGAGGAA	3993
rs142278602	snp	A/G	1.76699e-05	0.00297231	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573604	CTGGTAACGGTGCGG[A/G]CCCCAAGAAGGCCCC	3993
rs142284154	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543257	CCAGGGTGCATGGGC[A/G]GTCACTGTGAAGCTG	3993
rs142305370	snp	G/T	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75551561	GGGTGGTTGAAGGAT[G/T]GGCCCAACCCTTTGT	3993
rs142336264	snp	C/T	5.09005e-05	0.00504457	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571091	TTTGCTGACACCTAC[C/T]TGAAGGACAGTGAGT	3993
rs142394959	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75569506	TTCTTCTCCAGAAAT[C/T]GGAATTAAGGGCTGG	3993
rs142421479	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75544005	GATTCCTTCTGGCTC[C/T]GGCCGGGGTGAGTGG	3993
rs142470614	snp	A/C	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566824	GAGGACTTAATGTCT[A/C]CTCTGATCTCCAGAC	3993
rs142481289	snp	G/T	0.000153988	0.00877328	splice-donor-variant	LLGL2	GRCh38.p7	17:75568840	CCTGCTGCTCACAGG[G/T]TAGGGTACTTTGATG	3993
rs142537961	snp	A/C	0.396546	0.202545	intron-variant	LLGL2	GRCh38.p7	17:75558844	TCCTCCATCCGCACC[A/C]CACCTCCTCCATCCG	3993
rs142539407	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75529017	CAAAATTAGCCAGGC[A/G]TGGTGGTGAGCGCCT	3993
rs142615248	snp	C/T	0.000250077	0.0111793	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556095	CCCTCGGCTACAGCC[C/T]GTCCCTGCGCATCCT	3993
rs142710200	snp	C/T	0.000449427	0.0149837	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564428	CATCTCAGTGATCCA[C/T]GATGGCCAGCAGACG	3993
rs142772898	snp	C/T	0.0179658	0.0930597	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573585	GAAACCAAGAACCAC[C/T]GCCCTGGTAACGGTG	3993
rs142824531	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75557367	CTGGCAGGGACAGTC[C/T]TTCCCCGGCCTGAGG	3993
rs142843141	snp	C/T	0.0193772	0.0965046	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575381	TTTGTCTGAGCCCGG[C/T]GGTGCCTTCCCTCTG	3993
rs142874601	snp	C/T	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75554355	AGTGACTCACGCCTG[C/T]AATCCCAGCGCTTTG	3993
rs142947637	snp	A/C/G	0.000117776	0.00767309	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573131	CGAGCCGAGGACTAC[A/C/G]GGGAGCACCACCTGG	3993
rs142996464	snp	C/T	0.0119091	0.0762411	intron-variant	LLGL2	GRCh38.p7	17:75534072	GGCTGGATGGCCTGC[C/T]CACGCCAGCCCCAGG	3993
rs143012040	snp	A/G	0.000373117	0.0136535	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558583	CAAGGGCGGGGCATC[A/G]GAGCTGCAGGAGGAT	3993
rs143013538	snp	C/T	0.000186054	0.00964327	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571727	CCATCTATGCCTTCT[C/T]CCTGCGTGTGCCTCC	3993
rs143052264	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75526921	AGCTGTAATCCCAGC[A/G]CTTTGGGAAGCCAAG	3993
rs143145816	snp	C/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75563987	CTCAGCGGCCCAATT[C/G]CTGCCAAGTTCATTC	3993
rs143156079	snp	A/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75530707	TGTTGTCCCAATTAC[A/T]TGGGATCGTAGGAGG	3993
rs143274029	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531082	TACACCCTCCTCACC[C/G]TGCTGGGTGGCAGGG	3993
rs143319696	snp	C/T	9.20832e-05	0.00678477	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570399	GGGCCCACTCTCCCG[C/T]GTCAAGTCCCTCAAG	3993
rs143338056	snp	A/G	0.00842199	0.0643434	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563152	CTACAGGGCAGCCGC[A/G]TGCTCTACCACTTCC	3993
rs143411901	snp	A/G	0.0142736	0.0832652	intron-variant	LLGL2	GRCh38.p7	17:75550460	AGGAGTTGGGGGTGG[A/G]ATCCAAGGGGGTGGG	3993
rs143518179	snp	C/T	0.000826216	0.0203083	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563434	GCGAAGCCCAGCAAC[C/T]AGAGCCCCTCCGCAG	3993
rs143624894	snp	C/T	0.0004317	0.0146855	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569226	CCTTCTCCAGGTGGG[C/T]TCCTTTGACCCCTAC	3993
rs143687998	snp	A/G	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75547143	ACCCACACCAAGCCC[A/G]ATGCCTCAAAGAGAG	3993
rs143716175	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561984	CACTCTTGATTCAAA[C/T]TCTAATGTCAGTGAG	3993
rs143766866	snp	A/G	5.03537e-05	0.0050174	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573061	GAAGTTGAAGCTGAC[A/G]GCCCTGGAGGGCTCA	3993
rs143788402	snp	A/T	0.00676609	0.0577691	intron-variant	LLGL2	GRCh38.p7	17:75553095	TGTCCTGCACATCCT[A/T]TCCCACTGTCTACTC	3993
rs143816663	snp	C/T	0.000153988	0.00877328	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574653	GCCGTGGGGTGCAGC[C/T]TCAGCAATGGCGGAG	3993
rs143832162	snp	A/G	0.0263992	0.111815	intron-variant	LLGL2	GRCh38.p7	17:75562638	CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC	3993
rs143887617	snp	A/G	1.72812e-05	0.00293944	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570023	GAGCAGGTGGAGGCC[A/G]ACCTGCTGCAGGACC	3993
rs143945375	snp	C/T	0.000139997	0.00836535	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573256	TGGCATCGCCTCCTG[C/T]GTCTTCACCAAATAT	3993
rs143949135	snp	C/T	0.0130921	0.0798413	intron-variant	LLGL2	GRCh38.p7	17:75563547	TTCTGAAGCAAACTC[C/T]AGGGCCAGAGAGGGT	3993
rs143957131	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75544301	GTGATCCTCTTCCCC[C/T]GGGGAGCCAGGACCC	3993
rs143984858	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75536171	AGTTAGTGGGGTGGA[C/G]AAGGTTTTCCTGAGA	3993
rs143998947	snp	A/G/T	0.00235722	0.0342513	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570237	TTGACCACCAGCAGC[A/G/T]GCGGCAGGTCTTTGT	3993
rs144008601	snp	C/T	0.000116431	0.00762902	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568675	CGGCAGCCGGCAGAA[C/T]GCACACTTCTCCACC	3993
rs144193988	snp	A/G	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75551927	TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	3993
rs144195122	snp	C/T	3.3222e-05	0.00407553	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556117	GCGCATCCTGGCCAT[C/T]GGCACCCGTTCTGGA	3993
rs144196024	snp	A/G	0.0448719	0.142907	intron-variant	LLGL2	GRCh38.p7	17:75557540	CAAGGGAGTTGAGAG[A/G]TGAGGGACCACCTCC	3993
rs144254611	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75528091	CCAGACCCGTTAGTA[C/T]AAATAACTTTTTATT	3993
rs144259049	snp	C/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75558327	GGAGAGGCTGGCATT[C/T]GGTGGCCCTGGGTTT	3993
rs144347921	in-del	-/AAACAAAC			intron-variant	LLGL2	GRCh38.p7	17:75528739	CAAAACTCCATCTCA[-/AAACAAAC]AAACAAACAAACAAA	3993
rs144386071	snp	C/T	0.0022842	0.0337177	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573500	CTACCTGATCTCACC[C/T]TCGGAGTTTGAGCGC	3993
rs144426921	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75547116	CAACACCTTTTGGCT[C/T]AACTCCTTTATACCC	3993
rs144506761	snp	A/G	5.07052e-05	0.00503488	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571747	CGTGTGCCTCCCGCC[A/G]AGCGGAGAATGGATG	3993
rs144528048	snp	A/G	0.000265966	0.0115288	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543479	GGGAGAGGCTCAAGC[A/G]GGACCTGTTCCAGTT	3993
rs144534331	snp	A/G	0.00716266	0.059414	intron-variant	LLGL2	GRCh38.p7	17:75551437	ATACAAAGCTTAGTG[A/G]GTCTGACTCAGTCCC	3993
rs144556380	snp	A/G	0.000119786	0.00773813	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571926	GCTGATGCACCGGGC[A/G]CCGGTGGTGGGCATC	3993
rs144662042	snp	C/T	0.0260936	0.111202	LLGL2, TSEN54, LOC107985023	17	allele_origin=T(germline)/C(germline)	17:75524299	CTCTGCAGCCTCAAG[C/T]GGTTGTCTTACCAGA	3993
rs144751058	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563795	AATCCTCTGGCTGAC[C/T]ACTAGGCAGGGGTAG	3993
rs144775644	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75560833	AAAAAAAAAAAAAAA[A/C]AAAGAAAAAACATTT	3993
rs144804870	snp	A/G	0.00557542	0.0525036	intron-variant	LLGL2	GRCh38.p7	17:75559821	AGGTTCCATTTGCTC[A/G]CAAGCTCCGTGGCTA	3993
rs144813425	snp	A/G	0.0170251	0.090679	intron-variant	LLGL2	GRCh38.p7	17:75559739	CGCAGCGGGGAAGTC[A/G]GGCCCAGACCTCCCT	3993
rs144856011	snp	C/T	0.000270389	0.0116242	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570154	GCCCCCGGCTGTGGT[C/T]ACCTCCTTGGCCCTG	3993
rs144872065	snp	C/T	0.0260105	0.111035	intron-variant	LLGL2	GRCh38.p7	17:75526632	TGAGTGAGGAGGGCG[C/T]CCCTTCCCCTGGGGA	3993
rs144919589	snp	A/G	0.000134694	0.00820541	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559380	GTGCGCTGGAGGACC[A/G]GACCATCAGCTCGGA	3993
rs145089635	snp	C/T	0.000365838	0.0135198	stop-gained, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574632	AACTGGCGTTCACAT[C/T]GAGCCGCCGTGGGGT	3993
rs145089698	snp	C/T	0.00962687	0.0687078	intron-variant	LLGL2	GRCh38.p7	17:75568728	CAGCCCCAGCCCCAC[C/T]GCAAGCCAAACTCTC	3993
rs145168317	snp	A/G	0.00323143	0.0400658	intron-variant	LLGL2	GRCh38.p7	17:75574089	GTGTTTGGGCTGGGA[A/G]TAGAGACGGCATTCC	3993
rs145181414	snp	C/T	0.00025223	0.0112273	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573166	CCTTACCAACCTGGG[C/T]GACATCCAGGTGGTC	3993
rs145247724	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75545720	AGGAAAGATAAACCT[A/G]GAGATGTTTTTACCC	3993
rs145268615	snp	C/T	0.030665	0.119967	intron-variant	LLGL2	GRCh38.p7	17:75572768	GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG	3993
rs145397879	snp	A/G	0.0170251	0.090679	intron-variant	LLGL2	GRCh38.p7	17:75545580	AGGATTTGGGATCCC[A/G]TCTGCCCTGCCCCTC	3993
rs145431209	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75527331	CTAGCTGTGGCAGAC[A/G]GAACTCAAACTCAGC	3993
rs145494716	snp	A/C	0.130351	0.219509	intron-variant	LLGL2	GRCh38.p7	17:75558864	TCCTCCATCCGCACC[A/C]CGCCTCCTCCATCCG	3993
rs145502124	in-del	-/GACA	0.0372196	0.131242	intron-variant	LLGL2	GRCh38.p7	17:75549193	CCTATTGGAGGGATG[-/GACA]GACAGACAAGTCAGC	3993
rs145540577	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75555321	TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC	3993
rs145632514	snp	A/G			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541915	TTTGTATTTTTAGTA[A/G]AGACGAGGTTTCACC	3993
rs145687567	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75557765	TGGTGCCAAGACTAA[C/T]GGGCCAAGGCTGTTG	3993
rs145692150	snp	A/C/G	0.0748431	0.178382	intron-variant	LLGL2	GRCh38.p7	17:75548371	CAACCTCTGCCTCCC[A/C/G]GGTTCAAGGGATTCT	3993
rs145704166	snp	C/T	0.000431306	0.0146788	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558230	GATCCACCTCCTGCC[C/T]GGCCAGGTGAGGGAC	3993
rs145731607	in-del	-/AA	0.246485	0.249975	intron-variant	LLGL2	GRCh38.p7	17:75538915	CTTTTTTTTAGAAAC[-/AA]AGAGTCTCGCTCTGT	3993
rs145746932	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75553659	GTTGACATAGCATCG[C/T]TTTGTGCTGTTCTCA	3993
rs145774754	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75543787	TTCCCTACCTGTATC[A/G]TGGGAATAAAACGAT	3993
rs145791488	snp	G/T	0.0174175	0.0916809	intron-variant	LLGL2	GRCh38.p7	17:75552832	CCATACTGCAAGTGC[G/T]TGGTGGCCCCATGGG	3993
rs145904171	snp	C/G/T	0.0108105	0.0727212	intron-variant	LLGL2	GRCh38.p7	17:75546198	TGCCAGGCCTTGGGA[C/G/T]GGGGAGCCCAGGCCA	3993
rs145928772	snp	A/C/T	0.000145927	0.00854075	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570360	AAGGTGCACACTGCA[A/C/T]CCCAGTGACCAGCTG	3993
rs145931580	snp	G/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75540265	GCAGAGAACCTGCTT[G/T]TCTGGGGTGGGGAGC	3993
rs145998384	snp	A/C	0.178144	0.239451	intron-variant	LLGL2	GRCh38.p7	17:75527919	CAGCCTTCTGAGTAG[A/C]TGGGACTACAAGCGC	3993
rs146029134	snp	A/G	0.000483345	0.0155383	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556096	CCTCGGCTACAGCCC[A/G]TCCCTGCGCATCCTG	3993
rs146092301	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75557398	CTGGATGTTGTCCAG[C/T]TGGGTCATCTTTTAT	3993
rs146152295	snp	C/T	0.000219912	0.0104837	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571732	TATGCCTTCTCCCTG[C/T]GTGTGCCTCCCGCCG	3993
rs146173157	snp	C/G/T	0.0263992	0.111815	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567856	CTGAGGCAGGAGGAT[C/G/T]GCTTGAACCTGGAGG	3993
rs146215094	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535879	CAGAAATATTTTGCC[A/G]GCCAGGTGCAGACGT	3993
rs146255705	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523964	TACTCTGAGCTCCTC[A/G]TTGCTGGCATTTTAG	3993
rs146301005	in-del	-/T	0.316	0.241131	intron-variant	LLGL2	GRCh38.p7	17:75527962	ACAGCTAATTTTCTA[-/T]TTTTTTTTTAGAAAG	3993
rs146320210	snp	C/T	0.000102365	0.00715345	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75572003	TGGCCCATGATCTGT[C/T]GAAGAGCCCTGACAT	3993
rs146325197	snp	A/G	0.0193772	0.0965046	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567060	GGGACAGCTGAGCCC[A/G]GGCACCCTCAAGCCT	3993
rs146377375	snp	A/G	0.0263992	0.111815	intron-variant	LLGL2	GRCh38.p7	17:75540065	TCCCCCTTTACAGAG[A/G]AGCTGTCTCTGGAGG	3993
rs146433900	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75536306	ACTTGTCTCTTCTCC[A/G]CATTCCTCCCAGGTG	3993
rs146449794	snp	A/G	3.37747e-05	0.00410928	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563446	AACCAGAGCCCCTCC[A/G]CAGCCTCGTGCCTTA	3993
rs146515539	snp	A/G	0.00755907	0.0610114	intron-variant	LLGL2	GRCh38.p7	17:75533526	GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT	3993
rs146566626	snp	A/G	0.0252325	0.109451	intron-variant	LLGL2	GRCh38.p7	17:75569545	CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	3993
rs146566964	snp	C/T	0.00557542	0.0525036	intron-variant	LLGL2	GRCh38.p7	17:75533595	AGGCATGAGCCACCG[C/T]GCCCAGCCCGTTCAA	3993
rs146655914	snp	C/T	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75533062	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	3993
rs146673111	snp	A/G	0.00676609	0.0577691	intron-variant	LLGL2	GRCh38.p7	17:75564112	TCTGGGTGATGTTCA[A/G]ACAGAATTGGTGGGG	3993
rs146674354	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530224	TTTAAAGTCTCTGGC[G/T]GGGCATTTTGGCTCA	3993
rs146711859	snp	A/G	0.000221777	0.010528	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569100	AGAACTTCAGTGCCC[A/G]GGGCGAGGACGAGTG	3993
rs146753054	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75561153	GGCAGTTTAAATTCT[C/T]GTCCTCTTGATGACA	3993
rs146995958	snp	A/G	0.0182019	0.0936463	intron-variant	LLGL2	GRCh38.p7	17:75538058	TCAAGTGATCAGCCC[A/G]CCTTGGCCTCCCAAA	3993
rs147027220	snp	A/G	3.60192e-05	0.00424362	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569990	GAACTGAATGACGAG[A/G]CAGCGGAGCAGGCTG	3993
rs147218924	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75547439	CTTAGCCTCTCTGTT[C/T]TTTAGTTTCCTCATC	3993
rs147270979	snp	C/T	0.00138304	0.0262604	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570025	GCAGGTGGAGGCCGA[C/T]CTGCTGCAGGACCAA	3993
rs147321138	in-del	-/CT			intron-variant	LLGL2	GRCh38.p7	17:75573694	CCCTCTCTGAGATAC[-/CT]CGAGGCTCCCACTGC	3993
rs147326996	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559109	GTCTTGGCAGAAAGT[A/G]ACCAATGTTTGTCCT	3993
rs147468219	snp	C/T	0.00953873	0.0683987	intron-variant	LLGL2	GRCh38.p7	17:75534552	GTGGTGCCATCATAG[C/T]TCACTGCAGCCTCAA	3993
rs147490444	snp	A/G	0.000133645	0.00817342	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564471	ACCTCCCGTGTCATC[A/G]GCTTCACTGTCCTCA	3993
rs147537279	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75531300	TGTGGGAGATCTGCG[C/T]ATCTCTGGCAAGAGC	3993
rs147586963	snp	C/T	0.0494327	0.149241	intron-variant	LLGL2	GRCh38.p7	17:75553224	GGCTGGCCTGGGGGC[C/T]GCTGCTGGGCCCTAT	3993
rs147590883	snp	G/T	0.178144	0.239451	intron-variant	LLGL2	GRCh38.p7	17:75527918	TCAGCCTTCTGAGTA[G/T]CTGGGACTACAAGCG	3993
rs147605316	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545125	CCCCTACCCCTGCCC[C/T]CTTGCACCAAGTTCT	3993
rs147621995	snp	C/T	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541874	AGCTGGGATTACAGG[C/T]GTCTGCCACCACACT	3993
rs147740967	snp	A/C/G	0.000182593	0.00955342	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558231	ATCCACCTCCTGCCC[A/C/G]GCCAGGTGAGGGACC	3993
rs147750930	snp	C/T	6.80226e-05	0.00583152	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563364	TGGCAGCGGGACGGC[C/T]GCCTGCTCGTCAGCT	3993
rs147831761	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75569412	CAACCACCTGCCTAA[C/T]GCACATTCTGTGTCC	3993
rs147856534	snp	A/T	0.00209718	0.0323139	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573509	CTCACCCTCGGAGTT[A/T]GAGCGCTTCTCTCTC	3993
rs147864220	snp	C/T	0.000838926	0.0204636	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570196	GCGGCTCGTGGCCTT[C/T]GGCACCAGCCATGGC	3993
rs147921007	snp	A/G/T	0.0678174	0.1712	intron-variant	LLGL2	GRCh38.p7	17:75528185	CAGTGGCGAGATCTC[A/G/T]GCTCACTGCAAGCTC	3993
rs147987206	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB, downstream-variant-500B	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523112	TGAACCTGGGAGGCA[A/G]AGGTCACAGTGAGCC	3993
rs147991148	snp	A/G	0.000214686	0.0103584	utr-variant-3-prime, missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574889	AGTGAGTGGCTGAGC[A/G]TCCAGGCTGCGCGAT	3993
rs148020757	snp	A/G	0.0134227	0.0808156	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571720	GGGGGCACCATCTAT[A/G]CCTTCTCCCTGCGTG	3993
rs148054484	snp	G/T	1.65902e-05	0.00288008	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569245	TTTGACCCCTACAGT[G/T]ATGACCCCCGGCTGG	3993
rs148058066	snp	A/G	0.00914312	0.0669923	intron-variant	LLGL2	GRCh38.p7	17:75556776	AAAAAAATTTTTTTC[A/G]GCACTTTGGGAGGCT	3993
rs148178937	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567459	ACAAGAGCGAAACTC[C/T]GTCTCAAAAAATAAA	3993
rs148195845	snp	A/G			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575293	CCCTGCCTGTCCCCC[A/G]AGGCTCCAGCCCTGG	3993
rs148339508	snp	C/T	0.0614824	0.164198	intron-variant	LLGL2	GRCh38.p7	17:75539493	AAGTGATCCTCCCAC[C/T]TTGGCCTCCCAAAGT	3993
rs148356188	snp	A/T	0.00914312	0.0669923	intron-variant	LLGL2	GRCh38.p7	17:75548966	ACAACTCAGGATGGG[A/T]GTTGCTTCCATTCTG	3993
rs148381816	in-del	-/AG	0.0445539	0.14245	intron-variant	LLGL2	GRCh38.p7	17:75555871	GAGTCACAAAGGGAC[-/AG]GGGGTGGGGCCTGGT	3993
rs148419840	snp	A/G	0.000321041	0.0126656	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571751	TGCCTCCCGCCGAGC[A/G]GAGAATGGATGAGCC	3993
rs148421668	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75560142	CAGCTCTCCAGCCCT[C/G]GGTGGTGATGAAGCA	3993
rs148459948	snp	A/G	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75551536	CTTGAAGGGAATGAG[A/G]AATGAATGCGGGTGG	3993
rs148507255	in-del	-/GCGAAG			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543021	TGGAGGAAGAGGCTT[-/GCGAAG]TTTCCCTTTCTGCTT	3993
rs148580993	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557594	CGGAGCCTGACCTCC[C/T]TCTTCCCCTCTGCCC	3993
rs148650299	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544350	AGGACATGTGGCTTT[C/T]GTTGGGGGCTTCCGT	3993
rs148701538	snp	A/G	0.00998283	0.0699411	intron-variant	LLGL2	GRCh38.p7	17:75569142	GCAAGGTGAGGCCAG[A/G]AGCCTGGGACCCAGG	3993
rs148746317	snp	C/T	0.00144119	0.0268052	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559398	CCATCAGCTCGGACG[C/T]GGTGCTGCAGCGGTG	3993
rs148797299	snp	A/G	0.00708711	0.0591044	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568831	CCAGAGGGACCTGCT[A/G]CTCACAGGGTAGGGT	3993
rs148822621	snp	A/C/T	6.75463e-05	0.00581113	missense, synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563420	GTGGCCCGTGTCCAG[A/C/T]GAAGCCCAGCAACCA	3993
rs148825089	snp	A/G/T	0.0101488	0.0705091	intron-variant	LLGL2	GRCh38.p7	17:75555998	AGCAGCCATGGTGGC[A/G/T]CGAAGGGGACAGGTC	3993
rs148945135	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573022	CCCCCAGGTGTTCAC[A/G]CTGCCCAAGGTGAGT	3993
rs148946558	snp	C/T	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75561656	CCGGGCGCGGTGGCT[C/T]ACGCCTGTGATCCCA	3993
rs148981113	snp	A/C	0.00636936	0.0560724	intron-variant	LLGL2	GRCh38.p7	17:75552995	GGAAAGTGCTGCTGT[A/C]CTGGGAGACGGCTCC	3993
rs149034189	snp	A/G	0.0126979	0.078662	intron-variant	LLGL2	GRCh38.p7	17:75526768	TTCTGAGCAGGGAGC[A/G]GGCAGGGAGGGAATG	3993
rs149085980	snp	A/G	0.0263992	0.111815	intron-variant	LLGL2	GRCh38.p7	17:75530410	AATTCCAGCACTTTG[A/G]GAGGCCGAGGCAGGC	3993
rs149100966	snp	A/G	0.00325525	0.0402123	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570965	GCACAGGAGGGGAGT[A/G]CCAAGGCTGAGCGGC	3993
rs149106359	snp	C/T	0.0267878	0.112589	intron-variant	LLGL2	GRCh38.p7	17:75536368	GCCAAGCCCGCTCCC[C/T]GGCCCTGCTTTAAAG	3993
rs149157329	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75533583	TGCTGGGATTGCAGG[C/T]ATGAGCCACCGCGCC	3993
rs149176436	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545747	ACCCTTTGGGCAAGG[C/T]AGGTAAGCTCAGAGC	3993
rs149201295	snp	A/G	1.65181e-05	0.00287381	upstream-variant-2KB, missense, synonymous-codon, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523715	GATGTTTACCAGGCC[A/G]ACGCTGTGGCCACAT	3993
rs149301175	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75560837	AAAAAAAAAAACAAA[A/G]AAAAAACATTTTTTT	3993
rs149303269	snp	C/T	0.000132974	0.00815288	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75543478	CGGGAGAGGCTCAAG[C/T]GGGACCTGTTCCAGT	3993
rs149332090	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75551099	GACAGGTCATTTACA[C/T]ATGAAACCATTCTCT	3993
rs149346135	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75564443	CGATGGCCAGCAGAC[A/G]GCCTTCGACTTCACC	3993
rs149347379	snp	A/G	0.0170251	0.090679	intron-variant	LLGL2	GRCh38.p7	17:75557482	AACCGGATCAGGTTG[A/G]GCACCCCGCCAGTCT	3993
rs149399124	snp	A/G	0.000166176	0.00911376	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570145	GCAGTGTCAGCCCCC[A/G]GCTGTGGTCACCTCC	3993
rs149471472	snp	C/T	0.00068026	0.0184301	intron-variant	LLGL2	GRCh38.p7	17:75563481	CAGTGTTTCACCCGC[C/T]GGGCAGGGCCCACCC	3993
rs149495504	snp	A/G	3.46939e-05	0.00416482	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573248	GACGTCAGTGGCATC[A/G]CCTCCTGCGTCTTCA	3993
rs149561438	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75527933	GCTGGGACTACAAGC[A/G]CGCAGCACCATGCAC	3993
rs149568981	snp	C/T	0.000257001	0.0113329	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559396	GACCATCAGCTCGGA[C/T]GCGGTGCTGCAGCGG	3993
rs149668354	snp	C/T	0.00176301	0.0296378	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563390	CAGCTGTCACTCTGA[C/T]GGCAGCTACTGCCAG	3993
rs149682760	snp	A/C	0.0267878	0.112589	intron-variant	LLGL2	GRCh38.p7	17:75535838	TCCAAGTGGGTGTCC[A/C]GGTGTGTGGACACCT	3993
rs149733034	snp	A/G	0.00557542	0.0525036	intron-variant	LLGL2	GRCh38.p7	17:75540975	CTACAATGGGCACAG[A/G]TTACTTGAGCAAAAT	3993
rs149736062	in-del	-/T	0.245916	0.249967	intron-variant	LLGL2	GRCh38.p7	17:75534028	TTTAGGGCAGGTAGG[-/T]GAGGCCCTAGAAAGG	3993
rs149751383	snp	A/G	0.0532157	0.154195	intron-variant	LLGL2	GRCh38.p7	17:75572392	GCATGGGCCAGGCGC[A/G]GTGGCTCATGCCTGT	3993
rs149804622	snp	C/T	0.0599851	0.162463	intron-variant	LLGL2	GRCh38.p7	17:75548320	TTAGCTCTTGTTGCC[C/T]GGGCTGGAGTGCAAT	3993
rs149829375	snp	A/G	6.60567e-05	0.00574665	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75558180	CCAGGCGTGGAGTTC[A/G]TGGGGCTGCACCAGG	3993
rs149855459	snp	A/C	0.00835141	0.0640778	intron-variant	LLGL2	GRCh38.p7	17:75552136	CTGTCTTTAAAAAAA[A/C]AGTCTAGAAGCTGCA	3993
rs149872378	snp	A/G	0.0490535	0.14873	intron-variant	LLGL2	GRCh38.p7	17:75558819	CTGCCTCCTCCATCC[A/G]CACCACGCCTCCTCC	3993
rs149872906	snp	A/G	3.48511e-05	0.00417425	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569081	ACCGACACGGACCCC[A/G]ACGAGAACTTCAGTG	3993
rs149923284	snp	A/C	2.94399e-05	0.00383655	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570436	TTGCGTCAGTCATTC[A/C]GCCGGATGCGTCGGA	3993
rs149945830	snp	A/C	0.000689394	0.0185532	intron-variant	LLGL2	GRCh38.p7	17:75568722	TGGCCCCAGCCCCAG[A/C]CCCACCGCAAGCCAA	3993
rs150123183	snp	C/T	3.29506e-05	0.00405884	upstream-variant-2KB, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524364	TCATGGTGACATCTC[C/T]TTCTACAGCTTCAGG	3993
rs150153253	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566132	GCAGACTGAGCTGGG[A/T]GGGCTCTTGGCTTGC	3993
rs150169668	snp	C/G	0.022715	0.104123	TSEN54, LLGL2, LOC107985023	17	allele_origin=G(germline)/C(germline)	17:75523677	GGCTGTTGGAGAAGT[C/G]TGGGGGCTTGGAAAT	3993
rs150206008	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543215	AGCCCTGAGGTGGGC[C/T]GGCCTCTAGATCTGA	3993
rs150255580	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546560	TGGGACAGGCCCAGC[A/G]GACAGGCGGAGGGCA	3993
rs150325508	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75549446	TGGGCCTTCCCTGCC[C/T]GTGCCCACCCTCCTC	3993
rs150327727	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75526508	GTGTCTTAGTTTGTT[A/C]CGGCTGGACGATTGG	3993
rs150344901	snp	A/C	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75561257	TAGGATAAGAATGAT[A/C]ATTGTAGGGCTGTTT	3993
rs150350305	snp	C/T	8.36729e-05	0.00646757	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559324	GCTCTACCTGGGCAC[C/T]GAGAGTGGCAACGTG	3993
rs150379214	snp	G/T	0.00517822	0.0506191	intron-variant	LLGL2	GRCh38.p7	17:75553726	GGCGGGGGTCAGATT[G/T]GGGTAACTGATTAAG	3993
rs150412778	snp	C/T	0.00507152	0.0501003	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570388	CTGGCCTTGGAGGGC[C/T]CACTCTCCCGCGTCA	3993
rs150440276	snp	C/T	5.62435e-05	0.0053027	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574613	TTGCCTGTGCAGGAG[C/T]GGCAACTGGCGTTCA	3993
rs150609196	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75530972	GCCAAGAGTGAGAGC[C/T]GGTTGCCTGGGAGTC	3993
rs150621720	snp	A/T	0.0414363	0.137845	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524743	TTCTTTTCTGCTGTT[A/T]CTGTATGTACTGGGT	3993
rs150649144	snp	C/G/T	0.000116263	0.00762361	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556123	CCTGGCCATCGGCAC[C/G/T]CGTTCTGGAGCCATC	3993
rs150659220	snp	A/G	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75535420	CTCTGGTTTCGGCTG[A/G]GTCTGGAGTCCTGCC	3993
rs150708101	snp	A/G	8.49567e-05	0.00651699	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75573228	ACAGCTGCATCCGCC[A/G]GGAGGACGTCAGTGG	3993
rs150727522	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544723	CCTCCCTGACCTCCC[C/T]GTTGGGAGAGGTGGG	3993
rs150818003	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75558905	CCTCCATCCACACCA[C/T]GCCTCCTCCATCCGC	3993
rs150850607	snp	A/G	5.03732e-05	0.00501837	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563139	TGTCATCTGGGACCT[A/G]CAGGGCAGCCGCGTG	3993
rs150868733	snp	A/C	5.10504e-05	0.00505199	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75563345	GCAACTGGAGAACAT[A/C]TGGTGGCAGCGGGAC	3993
rs150869543	snp	A/G	1.70374e-05	0.00291863	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571686	CCGGCACTGCCCCTC[A/G]CTGTGGGCTGGCACC	3993
rs150901657	snp	C/T	0.000123619	0.00786094	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568987	CCACAGGCACGAGGA[C/T]GGCACGGTGCGGTTC	3993
rs150971482	snp	C/G/T	3.38508e-05	0.00411394	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571766	GGAGAATGGATGAGC[C/G/T]TGTGCGGGCAGAGCA	3993
rs150973787	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75565427	GCCTCTATCTACCCT[A/G]TTCAGGGGAACCCCA	3993
rs151025037	snp	C/T	0.0244538	0.107838	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543104	ATTAACCTCAGGGCC[C/T]GCCGGCCCTCCTTGT	3993
rs151152308	snp	G/T	0.0414363	0.137845	intron-variant	LLGL2	GRCh38.p7	17:75527490	GGAGTTTCCCCTTTG[G/T]TGTCAGATTAATATG	3993
rs151167112	snp	A/G	4.61606e-05	0.00480397	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570400	GGCCCACTCTCCCGC[A/G]TCAAGTCCCTCAAGA	3993
rs151168645	snp	C/G	0.000249221	0.0111601	intron-variant	LLGL2	GRCh38.p7	17:75558633	GACCCCCAGGGTAAG[C/G]GCTCAATCCCCAGCC	3993
rs151172846	snp	A/G	0.000118541	0.00769781	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75559306	ACATTCCTCCTGCGA[A/G]CTGCTCTACCTGGGC	3993
rs151205527	snp	C/G	0.0429648	0.14013	intron-variant	LLGL2	GRCh38.p7	17:75530393	CGGTGTCTCACGCCT[C/G]TAATTCCAGCACTTT	3993
rs151255929	snp	C/T	0.0193772	0.0965046	intron-variant	LLGL2	GRCh38.p7	17:75546061	CTCCTGGTTTGAGAC[C/T]CATGGAATAGAGAAC	3993
rs151324576	snp	A/G	0.00676609	0.0577691	intron-variant	LLGL2	GRCh38.p7	17:75555070	TAGTACCAGCTACTC[A/G]GAAGGCTGAGGCAGG	3993
rs151332020	snp	A/G	1.71493e-05	0.0029282	upstream-variant-2KB, missense, intron-variant, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75523764	GCAAACCCTATGCCC[A/G]GATGTGCATTAGTGG	3993
rs181016656	snp	A/G	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75569622	AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT	3993
rs181025511	snp	G/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75560937	CCTGGGTTCAAGTGA[G/T]TCTCCTGCCTCAGCC	3993
rs181030681	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523493	TGTTCGTGTGTGTCT[A/G]GGGAAGAGGGAGAAT	3993
rs181042118	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544012	TCTGGCTCCGGCCGG[A/G]GTGAGTGGGGAGAGG	3993
rs181050713	snp	A/G/T			intron-variant	LLGL2	GRCh38.p7	17:75551017	CATAACTAACCTAGG[A/G/T]CTCCCCTGCCTCTCT	3993
rs181060503	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75532716	AGGCATGAGCCGCTG[C/T]GCCCAGCCCTCTAGT	3993
rs181177138	snp	A/G	0.00908019	0.0667656	intron-variant	LLGL2	GRCh38.p7	17:75570298	CTGGGAGTGGGGCCC[A/G]CGAGGACTCCCAGGA	3993
rs181178377	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551867	GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGAA	3993
rs181187825	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75533041	GTCTTGCTCTGTCGC[A/C]CAGGCTGGAGTGCAG	3993
rs181290381	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75563530	AGGTGCAGGTTGCTC[A/G]ATTCTGAAGCAAACT	3993
rs181293746	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547172	AGCAAGGACATCGCC[C/T]CGGGGGTCCTGAGAG	3993
rs181303197	snp	C/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75529072	GAGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGC	3993
rs181321985	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538091	GCTGGGATTACAGGC[A/G]TGAGCCACCTCGCCC	3993
rs181406724	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75556858	TGGTAAAACCCTGTC[G/T]CTACTAAAAATATTT	3993
rs181673573	snp	A/C	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75557007	GCACTCCAGCCTGGG[A/C]AACAGAGTGAGACTC	3993
rs181680139	snp	G/T			intron-variant	LLGL2	GRCh38.p7	17:75538376	CCCCACTTGTCTTCA[G/T]CCTGAAACATAGAAG	3993
rs181782857	snp	A/C	0.000235312	0.0108444	intron-variant	LLGL2	GRCh38.p7	17:75558019	CCCTAGGCTCCATGC[A/C]TGGGTCCTGCTGCCT	3993
rs181854853	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75528435	TAACTTTTTAATATA[C/T]CGCAACATTAAAAGA	3993
rs181857313	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75564101	GACAAAATCACTCTG[A/G]GTGATGTTCAAACAG	3993
rs181883261	snp	C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75570865	CTGTGGCCTGCCTTC[C/T]GATGCAAGGATCAGC	3993
rs181886364	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75552471	TCCAGGCGTGACAGG[C/T]GTGACCCTATCTCAA	3993
rs181894350	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534217	CCCAGAATGGGGGTG[C/T]GTTCCCACCTTCCAC	3993
rs182001129	snp	A/G	0.0197687	0.0974348	intron-variant	LLGL2	GRCh38.p7	17:75546857	TCCAGCAGACAGGCG[A/G]AGGGCAGGTCCAGCG	3993
rs182157446	snp	A/G	8.55147e-05	0.00653835	intron-variant	LLGL2	GRCh38.p7	17:75543535	GGAAGATGACCCCCA[A/G]GTTTTCGGCCAAGCA	3993
rs182180790	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566098	CTGATGGAAGGCTTG[C/T]CCTGTAGGGACCTGG	3993
rs182194785	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548451	CCCGGCTAAAGGACA[A/G]CTTTTCAGAGCTACT	3993
rs182198312	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530487	AAACATGTCTCTACT[A/G]AAAATACAAAAAATT	3993
rs182276865	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75538509	AGACCTCGCCTCCTC[C/T]GTTCATTCATTCATT	3993
rs182283633	snp	C/T	0.000153614	0.00876261	intron-variant	LLGL2	GRCh38.p7	17:75563205	CCAGGACATGGCAGG[C/T]GCCATGTTGCTCTCC	3993
rs182292505	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75545124	CCCCCTACCCCTGCC[C/T]CCTTGCACCAAGTTC	3993
rs182300360	snp	C/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526164	CGGAGTCCCCGGGCC[C/G]ACGTGCAGGCGCCAG	3993
rs182309362	snp	A/G	0.0134861	0.0810011	intron-variant	LLGL2	GRCh38.p7	17:75553449	GACTGACTGATGGGG[A/G]AGGCAGGTAGCAATT	3993
rs182421239	snp	A/T	0.00874735	0.0655527	intron-variant	LLGL2	GRCh38.p7	17:75560486	ATATTATATTATATT[A/T]TATTTTATTTCATTT	3993
rs182552222	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561125	GTGTGAGCCACCAGG[C/T]CCAGCCCCTTTTGGC	3993
rs182565945	snp	A/G	0.0123036	0.0774623	intron-variant	LLGL2	GRCh38.p7	17:75544288	GAACTGGGACACTGT[A/G]ATCCTCTTCCCCCGG	3993
rs182567823	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524064	TACAGGCTAAGAGTG[G/T]TGAGCACCTTGCTCT	3993
rs182681115	snp	C/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75561908	GCCTGGGCAACAGAG[C/T]GAGACTCCCATCTCA	3993
rs182708382	snp	A/C	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534581	AACCTCCTGGGCTCA[A/C]GTGATCTTCCCACCT	3993
rs182820842	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75554024	AAGTCATTTTAGGCC[A/G]GGTATGATGGCTCAC	3993
rs182848839	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75558879	CCGCCTCCTCCATCC[A/G]CACCCCACCTCCTCC	3993
rs183008571	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540429	GGTCCTCCTGGCTCC[A/G]TCACCCCATGCCCAT	3993
rs183109677	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75572444	CGAGGCGGGCAGATC[A/G]CAAGGTCAGGAGATC	3993
rs183126480	snp	A/C	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75548143	AATGCAAATATTCCG[A/C]AACCCAAAAGATTCT	3993
rs183130095	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75530298	GCTTGAACCCAGGAG[C/T]TCAAGACCAGCCTGG	3993
rs183131797	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75535705	AAGGCAAGTCCACCC[C/T]GTGTGGTTATTCTCT	3993
rs183143958	snp	A/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75541181	GCCTTGTCACTTTTA[A/T]GCCTGTGTGGAGTCT	3993
rs183429913	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544666	CTGGAGGGGATCTCC[A/G]TGACCTCCCTGTTGG	3993
rs183588423	snp	C/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75529751	CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC	3993
rs183654756	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75561492	ATTAGTTGGGCAAGG[C/T]GGCACACGTCTGCAG	3993
rs183722539	snp	C/T	0.0228947	0.104514	intron-variant	LLGL2	GRCh38.p7	17:75569822	AAAAAAAAAAAAATG[C/T]AGGAGAGCTGGGGTT	3993
rs183732419	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551342	TCACCAGTACCATCC[C/T]GTTTATTAGATGAGA	3993
rs183804556	snp	A/G	0.0123036	0.0774623	intron-variant	LLGL2	GRCh38.p7	17:75547602	GGCTGAGGTGGGTGG[A/G]TCACTTGAGGTCTGA	3993
rs183826424	snp	A/G	0.00993419	0.0697739	intron-variant	LLGL2	GRCh38.p7	17:75562212	GGGTCAAGGCTCCAG[A/G]GCCAGGCCAACTCAC	3993
rs183829979	snp	G/T	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75545323	ATATGCAAGAAGCAT[G/T]CATTGAGCACTTACT	3993
rs183843627	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75527632	TTTTTCTTTAATAAT[A/C]TGTTTTTTAATTTGT	3993
rs183853912	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563206	CAGGACATGGCAGGC[A/G]CCATGTTGCTCTCCC	3993
rs183873207	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575344	ATCCACTTGGGGAGC[C/T]GTGTGAATCAAACTG	3993
rs183904499	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541891	TCTGCCACCACACTC[A/G]GCTAACTTTTTGTAT	3993
rs183905886	snp	C/T			downstream-variant-500B, intron-variant	LLGL2	GRCh38.p7	17:75564817	TGCAGCGAACCAGGA[C/T]CATGCTACTGTACTC	3993
rs184056726	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75525141	GCTAAAAATTCCACC[A/C]GCTGTTGCAGACCCT	3993
rs184316386	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542586	GATTCTATGGTGGGC[A/G]GAGAGTTTAGGGGCC	3993
rs184404114	snp	A/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75559954	GGGTGGGAGAAGGGG[A/T]CGGGGCCCAAAAAAA	3993
rs184413632	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75543354	GGCCTAATCGATACC[A/T]GAGTGCCAGGACAGA	3993
rs184422290	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532890	CAGGGTAAGGAAGTT[C/T]CCTGAGAACCCTGTG	3993
rs184430209	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559668	CTGTGTAATGTCACC[A/G]ACTGTCAGTCCAGTG	3993
rs184450872	snp	G/T	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75537371	TTCTCAGGACTCTGA[G/T]ATAAAATGGTCCCTT	3993
rs184509759	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75555101	AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG	3993
rs184513196	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75536477	TGTCTCCCCGCCTTT[C/T]CGGGCCTAACTATTC	3993
rs184557382	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75556943	CTGAGATGGGAGAAT[C/T]GTTTGAACCTGGGAG	3993
rs184568638	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75555979	CGTCTGGTGCTGCAG[C/G]TGCAGCAGCCATGGT	3993
rs184683787	snp	A/G			downstream-variant-500B	LLGL2	GRCh38.p7	17:75575684	CTGTATGGCCAGTGC[A/G]TGGGGTTCTCCGGTG	3993
rs184703409	snp	A/G	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75538365	TGCATTGGGCCCCCC[A/G]CTTGTCTTCATCCTG	3993
rs184737336	snp	A/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75568372	CCAAGAACAGGGCTT[A/T]CTGGATCTGCAGATG	3993
rs184739309	snp	C/G/T	0.0228947	0.104514	intron-variant	LLGL2	GRCh38.p7	17:75550690	CTCGGGAGACTCAGG[C/G/T]GGATCACTTGAGCCC	3993
rs184750766	snp	C/T	0.0119091	0.0762411	intron-variant	LLGL2	GRCh38.p7	17:75532454	TTTGAGTCTGAGTCT[C/T]GCTCTGTCGCCCAGG	3993
rs185128371	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75546440	TGTGAGGACTACATG[A/T]GTTCCTGCACGAATC	3993
rs185229220	snp	G/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75562773	CAGGGTTTTGCCATG[G/T]TGGCCAGGCTGCTCT	3993
rs185241646	snp	G/T	0.0111196	0.0737302	intron-variant	LLGL2	GRCh38.p7	17:75544056	GAGCCGGAGTTGGCC[G/T]CGGACTACCCCAATC	3993
rs185247444	snp	C/T	0.0107246	0.0724382	intron-variant	LLGL2	GRCh38.p7	17:75528336	TAGCCAAGATGGTCT[C/T]GATCTCCTGACCTCG	3993
rs185253622	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523558	AACCCTCAAGTGGCA[A/C]CTCTGTGAGGCTGCT	3993
rs185269102	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566627	CCATATTGACAGGAA[A/T]AGGCAGGAGGCCAGA	3993
rs185283656	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75530775	ATGATGGCGCCACTG[C/T]ACTCCAGCCTGGGTG	3993
rs185384274	snp	A/C/T	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75549000	GGGAGGAGACTAAGG[A/C/T]CCCCAGGGCTTGCAC	3993
rs185391385	snp	A/G	0.0123036	0.0774623	intron-variant	LLGL2	GRCh38.p7	17:75547055	ACAGCTCGACCCCAG[A/G]TGGCTTGTAGACACT	3993
rs185399451	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75528544	AGGAGTTTGAGAGCA[A/G]CCTCACCAACATGGA	3993
rs185478185	snp	A/C			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567619	ACTCCAGCCTGGGTG[A/C]CAGAGCAAGACTCCA	3993
rs185803825	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75557317	CAAATTCCACCCCCA[C/T]TCCCACAGGCGGCAG	3993
rs185811155	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75538489	CCACCAGTCAGTCTC[A/C]GTGGAGACCTCGCCT	3993
rs185889958	snp	A/C	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75563565	GGCCAGAGAGGGTAA[A/C]GGCTTTGTCCAAAGC	3993
rs185896309	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75547278	AACTGGCTGTCAGAG[C/T]GGTAACTCCAGTTCA	3993
rs186006283	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75560981	GGATTACAGGTGCAC[A/G]CCATCACACCCGGCT	3993
rs186015370	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75539303	TGAGCTCAAGTGATC[C/T]TCCCACCGTAGCCTC	3993
rs186135127	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561154	GCAGTTTAAATTCTC[A/G]TCCTCTTGATGACAC	3993
rs186139012	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544376	TCCGTTTGGGCTCCC[C/T]TGCCCCCGAAAGGAA	3993
rs186156379	snp	A/C	0.0256215	0.110247	intron-variant	LLGL2	GRCh38.p7	17:75529290	CAACCTCTGCCTCCC[A/C]GGTTCAAGCAGTTCT	3993
rs186439686	snp	C/T	0.00318978	0.0398085	intron-variant	LLGL2	GRCh38.p7	17:75571244	GGCAGACTGCAGCCC[C/T]TGCCTGCTTACTCCC	3993
rs186440983	snp	A/C	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75553107	CCTATCCCACTGTCT[A/C]CTCCCCTTTTCCTGG	3993
rs186447711	snp	C/G			intron-variant	LLGL2	GRCh38.p7	17:75534349	CATAGGATAGATGGT[C/G]GGGGGAATGGAGGCT	3993
rs186516533	snp	A/C			intron-variant	LLGL2	GRCh38.p7	17:75558884	TCCTCCATCCGCACC[A/C]CACCTCCTCCATCCA	3993
rs186553085	snp	C/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75562100	CCCACATCCTTGCTG[C/T]TGGCTGTTGGTCCTG	3993
rs186565759	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545198	AGTTGTCCCTTCTTC[A/T]TTCCCCTATCCCCCA	3993
rs186571248	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2, LOC107985023	GRCh38.p7	17:75526351	GGGAGGGACTTCGGT[C/T]TCCGGCCTTTCTCCA	3993
rs186668084	snp	A/G	0.00438332	0.0466095	intron-variant	LLGL2	GRCh38.p7	17:75547696	TGGGTGTGGTGGCAC[A/G]CGCCTGTAGTCTCAG	3993
rs186679620	snp	A/T			intron-variant	LLGL2	GRCh38.p7	17:75565334	AGGGCCCTCTCCTAA[A/T]GATGCTGGCCTGAAA	3993
rs186685524	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548180	TAAAACCCTCTATTC[A/G]CAATCATTTTAGATG	3993
rs186692036	snp	A/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75530349	CTACAAAAATTTTTT[A/T]AAAAAATTAGCTGGG	3993
rs186805295	snp	A/G	5.10856e-05	0.00505373	intron-variant	LLGL2	GRCh38.p7	17:75570300	GGGAGTGGGGCCCGC[A/G]AGGACTCCCAGGACC	3993
rs186840993	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75533553	TCATGATCTGCCCGC[C/T]TCGGCCTCCCAAAGT	3993
rs186876465	snp	A/G	0.000307595	0.0123977	intron-variant	LLGL2	GRCh38.p7	17:75564334	CCCCAGCCCACTGCC[A/G]CTCCTCTGTGCCTGC	3993
rs186889396	snp	A/G	0.00279162	0.0372561	intron-variant	LLGL2	GRCh38.p7	17:75529899	AAAAAAAGATTTTTA[A/G]TGTCTTTCTAGGCTT	3993
rs187034064	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551947	CAGCCTGGCCAACAT[A/G]GTGAAACCCCATCTC	3993
rs187154492	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566548	ACAGCTACTCAGCCT[A/G]ATGCCATTGCAGAGC	3993
rs187200960	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75543572	GCTGGGGCTGAGGCA[C/T]CTCTTACCTGGATTA	3993
rs187332174	snp	G/T	0.0023933	0.0345097	intron-variant	LLGL2	GRCh38.p7	17:75540751	GACAGGGTGTTTTGC[G/T]GCTGTGGTCTGTTTC	3993
rs187418397	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75560568	CTTGGCTCACTGCAA[C/T]CTCTGCTTCCTGGGT	3993
rs187435073	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541568	TCTGGTCTGACTCCT[C/G]CAAAATGTGAAGGCA	3993
rs187521882	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75553650	AAGCAATCAGTTGAC[A/G]TAGCATCGCTTTGTG	3993
rs187608916	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542072	AGCACAGCAAGCCCT[C/G]GGTTCCTCTGCCCGA	3993
rs187766428	snp	A/G	0.00530315	0.0512197	intron-variant	LLGL2	GRCh38.p7	17:75572084	CACACGGGCAGCGGC[A/G]GGTCTCCCTGGGACT	3993
rs187781989	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75534681	AGACAAGGTCTCCCT[A/G]AGTTGCCCAGGCTGG	3993
rs188024421	snp	C/G	0.000399281	0.0141238	missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574252	AGCGCGCTCTGCTCA[C/G]TGATGAGAGTGAGTT	3993
rs188039356	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75555519	GTTGGAATTTGGTGA[C/T]AGTAAGAGTCTGTGA	3993
rs188047610	snp	C/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75536624	TGACCATGCCTGGGG[C/G]CTCTTTCCTTCTCTC	3993
rs188129364	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75563238	GGGCCCCAAGTGGCA[C/T]ATACACACTGTGCAG	3993
rs188135634	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75547084	CTGGCTTCTGAACCA[C/G]TTCTGGCCTTTTTGT	3993
rs188144499	snp	C/T	0.0146672	0.084371	intron-variant	LLGL2	GRCh38.p7	17:75530619	CGCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA	3993
rs188147720	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75528783	ATAATCCCAGGTGAT[C/T]GCTGTTCATTTAAAA	3993
rs188255842	snp	C/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75549357	TCGGCCAAACCCAGG[C/G]ACACCCCAAGCAGCC	3993
rs188290235	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75532502	GATCTTGGCTCACTG[C/T]AACCTCTGCCTCCCG	3993
rs188390256	snp	C/T	0.0252325	0.109451	intron-variant	LLGL2	GRCh38.p7	17:75572596	CGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	3993
rs188408283	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75535728	TATTCTCTCTCTCTG[C/T]CCCCACTGGTCTCTT	3993
rs188423893	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75548473	AGAGCTACTCCCATG[C/T]CTGCACTTTCTGAGA	3993
rs188525891	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75567059	TGGGACAGCTGAGCC[C/T]GGGCACCCTCAAGCC	3993
rs188543207	snp	A/T	0.00159617	0.0282053	intron-variant	LLGL2	GRCh38.p7	17:75538375	CCCCCACTTGTCTTC[A/T]TCCTGAAACATAGAA	3993
rs188547114	snp	C/T	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75531347	AGGAGTTTAGTTTCC[C/T]CGGGGAGCTATTCGG	3993
rs188679811	snp	A/G	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75554392	CGAGGCAGGAGGATC[A/G]CTTGAGTCTAGAAGG	3993
rs188680481	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75559738	CCGCAGCGGGGAAGT[C/T]GGGCCCAGACCTCCC	3993
rs188685943	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542638	GAGCAGATTCCTCCT[G/T]ATTATTCTCCACTAG	3993
rs188794705	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75559990	GAGATAGCATCTGAC[A/G]AGATCATGTTGGGGC	3993
rs188802446	snp	A/G	0.000673299	0.0183356	intron-variant	LLGL2	GRCh38.p7	17:75543511	AACAAGGTAAGTTAG[A/G]GAGAGCAGGGAAGAT	3993
rs188934466	snp	A/G	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75561567	TGGAGGCTGCAGTGA[A/G]CCATGATCAGGTCAC	3993
rs188942933	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75562655	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	3993
rs188951099	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	LLGL2, LOC107985023	GRCh38.p7	17:75525513	GGCCTGCGGAACCCC[A/G]AGGCCGTTCGCGAGG	3993
rs189040458	snp	A/G/T	0.000739002	0.0192107	intron-variant	LLGL2	GRCh38.p7	17:75556039	CCCCACGTGCTTCTC[A/G/T]TTGCAGACGGTGGAG	3993
rs189229294	snp	A/G			intron-variant	LLGL2	GRCh38.p7	17:75544824	ATGGAGCTTTGCCAC[A/G]AGGACATTTGCCTCT	3993
rs189319803	snp	C/T	0.00478085	0.0486577	downstream-variant-500B	LLGL2	GRCh38.p7	17:75575378	CGTTTTGTCTGAGCC[C/T]GGCGGTGCCTTCCCT	3993
rs189330771	snp	C/T	0.00398564	0.0444627	intron-variant	LLGL2	GRCh38.p7	17:75538057	CTCAAGTGATCAGCC[C/T]GCCTTGGCCTCCCAA	3993
rs189423960	snp	C/T	0.00993419	0.0697739	intron-variant	LLGL2	GRCh38.p7	17:75557923	TGGAGTTGCTCCCAC[C/T]GGCCTGACTGGGAAA	3993
rs189460474	snp	A/G	0.0001164	0.007628	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75568647	TGAAGCTGTGGGAGC[A/G]GATCATTGCCGCCGG	3993
rs189460732	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75550973	ATCCCAATCCCTTCC[C/T]TGTTCCCAACAAGAT	3993
rs189525210	snp	A/G	0.00199481	0.0315187	intron-variant	LLGL2	GRCh38.p7	17:75565627	CAGCGGAAAGGTCAG[A/G]AAGGGAGGGAAGAAA	3993
rs189527708	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75548402	CCAGCCTCAGCCTCC[C/T]ACATAGCTGGGATTA	3993
rs189703614	snp	A/G	9.56686e-05	0.00691557	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570096	GCTCAGGGCCCGTGC[A/G]CTTTGAGCCTGGCTT	3993
rs189719889	snp	C/T	0.000798403	0.0199641	intron-variant	LLGL2	GRCh38.p7	17:75533038	GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	3993
rs189959716	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75551617	CTGAGCCGAACAGGA[A/G]TAGTGACTCTGGTGA	3993
rs189994887	snp	A/G	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75545844	AGTGGGGATGGGAAC[A/G]AGGCATGAATTGAGC	3993
rs190201038	snp	A/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75540898	GACATTCAGCGACCC[A/T]TGACTGTGACTCTCT	3993
rs190257253	snp	A/G	0.00119737	0.0244387	intron-variant	LLGL2	GRCh38.p7	17:75528215	CCTCCTCCTGGGTTC[A/G]CGCCATTCTCCTGCC	3993
rs190334233	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561083	GTGATCCACCCACCT[C/T]GGTCTCCCAAAGTGC	3993
rs190346223	snp	A/G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75534192	TGGATTATGAAAGGG[A/G/T]GCTAAGGCCCCCAGA	3993
rs190348888	snp	C/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75544185	AGTGTGGCTCTTCAG[C/T]TCCCGGGCCACCAAG	3993
rs190352999	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TSEN54, LLGL2, LOC107985023	GRCh38.p7	17:75523598	TGGTGGAGGGAAAGG[A/G]TGGGATGGAAAAGAA	3993
rs190370947	snp	C/T	0.00478085	0.0486577	intron-variant	LLGL2	GRCh38.p7	17:75543930	CACAGGCCATGGCTG[C/T]TTCTCCCTTCTCAAA	3993
rs190459052	snp	G/T	0.000399281	0.0141238	intron-variant	LLGL2	GRCh38.p7	17:75561242	TCTGTCCTAAAGATA[G/T]AGGATAAGAATGATC	3993
rs190508507	snp	C/T	0.000159936	0.00894105	intron-variant	LLGL2	GRCh38.p7	17:75562981	ATTCCCCCTGGTGGA[C/T]GGCATCGGAGGCTCA	3993

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