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

NTNG2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs762564	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239954	TTCCTTCTCTACCCA[A/G]AAGCCAGTCCTTGAG	84628
rs762565	snp	C/T			synonymous-codon	NTNG2	GRCh38.p7	9:132239246	GTTCTCATCATCCAG[C/T]TGTGCCGAGCCGTTG	84628
rs762566	snp	C/G/T	1.66421e-05	0.00288458	missense	NTNG2	GRCh38.p7	9:132239244	TCTCATCATCCAGTT[C/G/T]TGCCGAGCCGTTGCG	84628
rs762567	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132235562	CATCACAGCCCCGCA[A/C]CCCACAGGCCCCTTA	84628
rs762568	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132235248	TGCGAAGTGGGACAT[C/G]TCTTCCGGCCAAGAT	84628
rs762569	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132235246	CGAAGTGGGACATCT[C/G]TTCCGGCCAAGATCT	84628
rs869497	snp	C/G	0.134119	0.221521	intron-variant	NTNG2	GRCh38.p7	9:132163667	CAGCGCCCTCCCTCC[C/G]GTGCCCCCAggggcc	84628
rs870591	snp	A/G	0.20111	0.245173	intron-variant	NTNG2	GRCh38.p7	9:132187384	TTTACGCTGATTCAC[A/G]AGCGGGGAGGGTGAC	84628
rs870592	snp	A/G	0.142609	0.225759	intron-variant	NTNG2	GRCh38.p7	9:132187388	CGCTGATTCACAAGC[A/G]GGGAGGGTGACCTTG	84628
rs871461	snp	G/T	0.311369	0.242351	intron-variant	NTNG2	GRCh38.p7	9:132201974	GCTGTCTGCCATGTA[G/T]TGGCGCTGTGCAATC	84628
rs871462	snp	C/T	0.491936	0.0629843	intron-variant	NTNG2	GRCh38.p7	9:132201909	CTTCATCTGAAAACA[C/T]GAGGCTGGGGGAGCG	84628
rs871463	snp	G/T	0.447938	0.152711	intron-variant	NTNG2	GRCh38.p7	9:132201866	GGAGCGCTCCAGGGG[G/T]TGGGGATCAGGTCTG	84628
rs874653	snp	A/G	0.45946	0.136478	intron-variant	NTNG2	GRCh38.p7	9:132211751	GGCTGTGGAATTGTC[A/G]CAAGCCGCCAAGGCT	84628
rs876952	snp	C/G	0.499965	0.00419314	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244085	GAGATGTAAGCAGGA[C/G]TGATGGGTGGGCTTC	84628
rs876953	snp	A/G	0.397813	0.201621	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244197	CTCATCCCTCCCTCT[A/G]CTCTTCAGTCAGCAG	84628
rs883318	snp	A/G	0.49975	0.0111793	intron-variant	NTNG2	GRCh38.p7	9:132167498	CCAGCAGACGGTACC[A/G]TGAAGCTAGAGCATG	84628
rs914418	snp	A/G	0.498945	0.022939	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244768	GGGTGAGTTCTGCTC[A/G]GCTGCCCTGTGCTCA	84628
rs914419	snp	C/T	0.308414	0.24308	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229672	ACCCACTCCTTCCTC[C/T]ACCTCCATGTCTGGG	84628
rs914420	snp	A/G	0.342134	0.232404	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229399	GGAGAGACTTGGAGC[A/G]GATGGAGGGAAGTTC	84628
rs914422	snp	A/C	0.0759472	0.179459	intron-variant	NTNG2	GRCh38.p7	9:132167798	CAGCAGAGATGGTTG[A/C]GTGCGAGCTGTCTGA	84628
rs914423	snp	A/G	0.498754	0.0249289	intron-variant	NTNG2	GRCh38.p7	9:132168589	GGAGAAGGCGGCACG[A/G]AGCCAGGAGCTGGGG	84628
rs914424	snp	A/G	0.499997	0.00119808	intron-variant	NTNG2	GRCh38.p7	9:132168648	GGGGACCGCAGGGCC[A/G]AGCAAGGGGGCTGGG	84628
rs928912	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132233741	ATATGATGATACAAT[C/G]ATACGAGCACAGCCC	84628
rs933173	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132236548	GGGCGCTCAAAGCCC[G/T]GCTCGCTGCTCAGAG	84628
rs933174	snp	A/G	0.481242	0.0950111	intron-variant	NTNG2	GRCh38.p7	9:132236183	CTTCTCCCTTCACCC[A/G]CCACAGTCCACCCTC	84628
rs943754	snp	G/T	0.286042	0.247388	intron-variant	NTNG2	GRCh38.p7	9:132233475	GGAAATGCAGGGGAG[G/T]TGAGGGTCCCCAGGA	84628
rs1041501	snp	C/G	0.490287	0.0690083	intron-variant	NTNG2	GRCh38.p7	9:132197600	CCACACCTGGTGACA[C/G]TGTGCCTGGGCCTCC	84628
rs1041502	snp	C/T	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132197492	CCCTTCCACTCTGTC[C/T]GCCTCAAAAATTCCC	84628
rs1041504	snp	C/T	0.490343	0.0688145	intron-variant	NTNG2	GRCh38.p7	9:132196622	TGAAAATGTCACTAA[C/T]GTAGTGGTCCCCAGG	84628
rs1105684	snp	A/T	0.27278	0.24896	intron-variant	NTNG2	GRCh38.p7	9:132164221	AAAATAAATAAATTT[A/T]AAAAACCCTAACAAC	84628
rs1105685	snp	A/G	0.301177	0.244706	intron-variant	NTNG2	GRCh38.p7	9:132164169	AATGTGTTTACAACT[A/G]GTCAATCAATTGGGC	84628
rs1111393	snp	A/C/T	0.000164694	0.00907302	intron-variant	NTNG2	GRCh38.p7	9:132239006	CAGGTCATGCAGGGA[A/C/T]GGAGGAAGGCATCTT	84628
rs1331625	snp	C/G	0.208474	0.246527	intron-variant	NTNG2	GRCh38.p7	9:132184100	CCCACCCCCAACGAC[C/G]AGCCAGGGTTCATCC	84628
rs1331626	snp	C/T	0.454061	0.144427	intron-variant	NTNG2	GRCh38.p7	9:132216512	CCCACTGCAGAATCC[C/T]ACGGCTTTAGCTCTT	84628
rs1331627	snp	C/T	0.499563	0.0147699	intron-variant	NTNG2	GRCh38.p7	9:132216492	CTTTAGCTCTTCAGA[C/T]GGCAGCAAGAACGCT	84628
rs1810887	snp	A/G	0.493925	0.054776	intron-variant	NTNG2	GRCh38.p7	9:132235069	CCCCAGCATGAACCA[A/G]TGACACAACGCTCAG	84628
rs1887625	snp	C/T	0.305934	0.243663	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230068	ACGGCACGATTTACG[C/T]AGGGGATGCTGACAC	84628
rs1887626	snp	G/T	0.312348	0.242101	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230210	CTGTCCTGCACTGGA[G/T]GGCCCAAAAATCTGA	84628
rs1977549	snp	C/G	0.493386	0.0571263	intron-variant	NTNG2	GRCh38.p7	9:132216416	acatacacacacaca[C/G]agagagagagagaga	84628
rs1999033	snp	A/G	0.49941	0.0171624	intron-variant	NTNG2	GRCh38.p7	9:132232031	AGTTCAGCTTCCAAA[A/G]TCGTCTTCCTCCTGC	84628
rs1999389	snp	A/G	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132175146	CTCTCTGTCACCCAC[A/G]CACTTTCCCCTCGAA	84628
rs1999391	snp	A/G	0.497749	0.0334707	intron-variant	NTNG2	GRCh38.p7	9:132234482	GTCTTGGGGAGGGAG[A/G]GAGTCCTGGCTTGGC	84628
rs2011023	snp	C/T	0.490398	0.0686206	intron-variant	NTNG2	GRCh38.p7	9:132197112	gtgagccactgcgcc[C/T]ggccCCTGAGCCTTT	84628
rs2023364	snp	C/G	0.403158	0.197592	intron-variant	NTNG2	GRCh38.p7	9:132216418	acacatacacacaca[C/G]acagagagagagaga	84628
rs2026367	snp	C/T	0.18325	0.240924	intron-variant	NTNG2	GRCh38.p7	9:132173447	GTGAAAGGGCCCAGA[C/T]GGGACATCTTTCCAA	84628
rs2104852	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132211949	tgttcatgaatgaat[A/C]aatgaatgactgact	84628
rs2149171	snp	C/T	0.471983	0.114993	synonymous-codon	NTNG2	GRCh38.p7	9:132226867	CAAGTGCAACCTGCA[C/T]GCCAACCTGTGCTCC	84628
rs2183763	snp	C/T	0.0482946	0.147699	intron-variant	NTNG2	GRCh38.p7	9:132196612	ACTAACGTAGTGGTC[C/T]CCAGGGTCAGAGGGA	84628
rs2274852	snp	A/C	0.499424	0.0169631	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243197	CGGAGGTGGCCACCG[A/C]GACACAGTATAAATC	84628
rs2274853	snp	C/T	0.449428	0.150759	intron-variant	NTNG2	GRCh38.p7	9:132238978	CTTTGGAAAAGGTAC[C/T]GGAAGGTGCCCTAGG	84628
rs2274854	snp	A/T	0.227369	0.248974	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230667	CCCTTTTTTCTCTCC[A/T]GCTTTTTCCAGGACA	84628
rs2274855	snp	C/T	0.375637	0.216137	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230557	CCTGTGGGAGAGAGA[C/T]GGGCGTGAGCTGGCT	84628
rs2361547	snp	A/G	0.498611	0.0263212	intron-variant	NTNG2	GRCh38.p7	9:132216572	GCCTGGGAGGGGTCC[A/G]CTGGCCTCATGGGCT	84628
rs2361548	snp	G/T	0.413914	0.188765	intron-variant	NTNG2	GRCh38.p7	9:132225155	CTCCTGACCTCAAGT[G/T]ATCTGCCTGCCTTGG	84628
rs2361549	snp	C/T	0.386884	0.209196	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239701	AGCCTATCCCTCCTC[C/T]TGCAGGGGCCCAGTT	84628
rs2479527	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230197	CCATACGATGTCCCT[C/G]TCCTGCACTGGAGGG	84628
rs2482300	snp	C/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242682	GGAGGAGGAGAGAAG[C/G]AAGGGGTGGGGGGCC	84628
rs2482301	snp	C/G			intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242863	TCTTTCTGTGTTGGG[C/G]ACGGTGGGCAGGTGT	84628
rs2482302	snp	C/G			missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240990	CGCGAGGGCGCGGCG[C/G]GCCCCAAGTGCGACG	84628
rs2482303	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241314	gcctggtgagatggg[A/G]ccgacccgggggcgg	84628
rs2769644	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230079	tacgcaggggatgct[C/G]acaccgtgcctggca	84628
rs2769645	snp	A/C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230096	caccgtgcctggcac[A/C/G]tgggacgcactcCAC	84628
rs2769646	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230640	GGCCCCCACTGCACG[A/C]GCCTCTTTGCATGTC	84628
rs2769647	snp	A/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230740	CTCTAATTACACCCC[A/T]TCTGCTTCTCCACCT	84628
rs2769648	snp	A/G	0.00835141	0.0640778	intron-variant, splice-donor-variant	NTNG2	GRCh38.p7	9:132231569	GTCTGCACAGCCGTC[A/G]TAAGTTGCTTCTCTG	84628
rs2769649	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132231603	TGTCCCCACCCCGGC[A/C]ACCCCCCAACCCTCT	84628
rs2769650	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132231996	CCTGTTCCTGAGCCC[A/T]GCCAGGGGATTCAGG	84628
rs2769651	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132235279	GCCATTAGCCAGAGA[C/G]ATCAGCTCAGAGAGG	84628
rs2769652	snp	C/T	0	0	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132237223	TCCTTCAGGAAGGGG[C/T]CCCACCTCCCTGGGC	84628
rs2769653	snp	C/T	0	0	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237671	TAAACTGAGTCTCTC[C/T]TCCCTACAGGCCTCC	84628
rs2769654	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237792	TAGCCCATCCCGGCT[C/T]CCCTGGGAGGTGTGG	84628
rs2769655	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132238275	AATCCCTGAGAGCCT[G/T]GCCCCAGGCAGTCAC	84628
rs2769656	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132238844	GCTGCCCATGGCCCT[C/G]CCTGGTTCCCTGGGG	84628
rs2769658	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239769	AAGTCCCTTCCCGTT[C/G]CTGGGCCTCAGCTTC	84628
rs2769659	snp	C/G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243051	CCCCACCTGTTAGGA[C/G/T]CCTCCCCACACTGAA	84628
rs2769660	snp	C/G			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243165	AGAATCCTAGCAGAG[C/G]TTGAATCCAATGCTC	84628
rs2777465	snp	C/G	0.281841	0.247964	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230424	CCTGCAGGTCATCAT[C/G]ATTGCTAGCAGTTGT	84628
rs2777466	snp	C/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231294	CGGTCTCTCCTTTCA[C/G]CCTTGCAAACCCCTC	84628
rs2777467	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132232069	GCCATTGCTTGGAAG[G/T]GCTCCCAGACCATTG	84628
rs2777468	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132232349	GAGCCTCTGGAGCTG[A/C]GTTTGGACACCGTGG	84628
rs2777469	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132235563	AAGGGGCCTGTGGGG[A/T]GCGGGGCTGTGATGC	84628
rs2777470	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132238733	CAGGTGGCATGACCC[G/T]GCCCTCCTTGCATGA	84628
rs2777471	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132238734	AGGTGGCATGACCCT[G/T]CCCTCCTTGCATGAA	84628
rs2854925	snp	G/T	0.477853	0.102875	intron-variant	NTNG2	GRCh38.p7	9:132233164	CCCACCACAGGCTCA[G/T]CAGCAAAGCACAGGT	84628
rs2854926	snp	C/T	0.140581	0.224783	intron-variant	NTNG2	GRCh38.p7	9:132233123	TGGGCCAACCTATGT[C/T]TGAAGTCCAGAATTC	84628
rs2854927	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132232438	GCCTGTCTGTGGCAG[A/C]CCCCTGAGGGGCAGG	84628
rs2854930	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132231605	AGAGAGGGTTGGGGG[G/T]TGGCCGGGGTGGGGA	84628
rs2854934	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230380	GGTGGATTATCCCAT[C/T]TCATCCTCACTTCAG	84628
rs2854936	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132241790	ACAGGGTGTGCGAGA[C/T]CCCGGGGGCGCCGTC	84628
rs2854937	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132238531	ATTAGCCTGAGCTtt[C/G]tgcaagtttgattga	84628
rs2854938	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132238516	gtgcaagtttgattg[A/T]tttgcaggatgctaa	84628
rs2854939	snp	C/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242469	GTGTGTGTAAGTGTG[C/G]TGGGAGGCAGGACGG	84628
rs3065875	in-del	-/CA/CACA			intron-variant	NTNG2	GRCh38.p7	9:132233349	ACACACACACACACA[-/CA/CACA]GAGGAATCCATTTGC	84628
rs3739928	snp	C/T	0.4941	0.0539917	intron-variant	NTNG2	GRCh38.p7	9:132198716	AACATCCCAAGAACC[C/T]GGTCATGTTCCACAT	84628
rs3739929	snp	A/G	0.184203	0.241186	intron-variant	NTNG2	GRCh38.p7	9:132198676	CATCCCAGGTATCCA[A/G]TAACGTCCCAGGTAA	84628
rs3739930	snp	A/G	0.173589	0.238037	synonymous-codon	NTNG2	GRCh38.p7	9:132198580	GATGTTGGAGATGGC[A/G]TAGAAGTACTTGTAG	84628
rs3813389	snp	A/G	0.0970103	0.197722	intron-variant	NTNG2	GRCh38.p7	9:132167193	ACCAGACCTGGACCA[A/G]GTCTTTGTCCCACCT	84628
rs3813391	snp	A/G	0.0944967	0.195752	intron-variant	NTNG2	GRCh38.p7	9:132232034	TCAGCTTCCAAAGTC[A/G]TCTTCCTCCTGCCCT	84628
rs3824574	snp	A/G	0.433635	0.169641	synonymous-codon	NTNG2	GRCh38.p7	9:132198490	GTCGGTGAGGGTGAA[A/G]AACTCCTTGAGGCCC	84628
rs3829759	snp	A/G	0.0785177	0.181917	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166779	GTCCCGCCTGACCCC[A/G]TCGCTGCCTCTCCAG	84628
rs3831218	in-del	-/G			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243062	GGAGGCAGCCTTTCA[-/G]TGTGGGGAGGCTCCT	84628
rs3842682	in-del	-/G	0.489376	0.0721049	intron-variant	NTNG2	GRCh38.p7	9:132232813	TGATCCTTCCCCCTT[-/G]GGGGGTGGCATTTCT	84628
rs3929787	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216428	ACACACACACACACA[C/T]ACACACACACACAGA	84628
rs4024040	snp	A/G	0.388398	0.208197	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240270	CTGACGTCACAGGGG[A/G]CCAGCTGCAGGGACA	84628
rs4413904	snp	C/T	0.0256215	0.110247	intron-variant	NTNG2	GRCh38.p7	9:132232973	GGGGGCAGCACACCC[C/T]ACCTCTTTCTACATC	84628
rs4962057	snp	A/G	0.0607341	0.163335	intron-variant	NTNG2	GRCh38.p7	9:132188804	GTAACCTCATTGAGC[A/G]TTCATTCATTCTCCG	84628
rs4962058	snp	A/C	0.177824	0.239355	intron-variant	NTNG2	GRCh38.p7	9:132227421	CCTTCGCCTTCTTGA[A/C]CCTGAAGGCTGGCAG	84628
rs4962170	snp	C/T	0.495095	0.0492773	intron-variant	NTNG2	GRCh38.p7	9:132179418	CGTCCCCTAAGCCCA[C/T]CTGCCAGCTGCGGTC	84628
rs4962173	snp	A/G	0.00963355	0.0687312	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230577	TCTCCCACAGGTGCC[A/G]CTGCAGGTTCCTTTG	84628
rs5026783	snp	C/T	0.370365	0.219117	intron-variant	NTNG2	GRCh38.p7	9:132225229	GCCCTTTTGTTTTGT[C/T]TTGTTTTGTTTTTGT	84628
rs5900969	in-del	-/CA			intron-variant	NTNG2	GRCh38.p7	9:132187542	AAGGAGAATGAGAAA[-/CA]CACACACACAGAGAG	84628
rs6597547	snp	C/T	0.497641	0.0342639	intron-variant	NTNG2	GRCh38.p7	9:132173502	CCAGACCTTTCCGGT[C/T]TGCGCATCCCCACCT	84628
rs6597548	snp	C/T	0.49823	0.0296997	intron-variant	NTNG2	GRCh38.p7	9:132173641	GGGGCAGGCAGTGGA[C/T]GGATGGACAGACGAA	84628
rs6597549	snp	A/G	0.0352966	0.128072	intron-variant	NTNG2	GRCh38.p7	9:132173757	atgagatggatggac[A/G]gacgaacggagaggc	84628
rs6597550	snp	A/G	0.0352966	0.128072	intron-variant	NTNG2	GRCh38.p7	9:132173761	gatggatggacggac[A/G]aacggagaggcaggc	84628
rs6597551	snp	A/G	0.499982	0.00299515	intron-variant	NTNG2	GRCh38.p7	9:132175336	GAAGGATTAGGCCAC[A/G]GGCTCTGAAGGAGCA	84628
rs6597552	snp	A/G	0.497855	0.0326773	intron-variant	NTNG2	GRCh38.p7	9:132175554	CGGGCCATGAGGAAC[A/G]GGAGAAACGGCAGAT	84628
rs6597553	snp	A/C	0.34101	0.232846	intron-variant	NTNG2	GRCh38.p7	9:132178547	GCCCAGGAAAGGGGA[A/C]CCCAGAAGCAGGTGG	84628
rs6597554	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132199726	ttcctagacaggaca[C/G]tccaacggcttatgg	84628
rs6597555	snp	A/T	0.464096	0.129085	intron-variant	NTNG2	GRCh38.p7	9:132206123	CCACAACTGTCAGGG[A/T]TACAGAGAAAGAACA	84628
rs6597556	snp	A/G	0.46014	0.13543	intron-variant	NTNG2	GRCh38.p7	9:132210308	CCCGCTCAAGTCCCA[A/G]TACTCAGGAGGTGCC	84628
rs6597557	snp	A/C	0.456214	0.141336	intron-variant	NTNG2	GRCh38.p7	9:132212224	CTGCAGGGGAAGAAG[A/C]AACCTTGCTGAAGTC	84628
rs6597558	snp	A/G	0.455977	0.141681	intron-variant	NTNG2	GRCh38.p7	9:132213108	TGAGGTCGGGAGCTC[A/G]AGACCAGCCTGGCCA	84628
rs6597559	snp	A/G	0.457037	0.140127	intron-variant	NTNG2	GRCh38.p7	9:132213261	TGGGAGGCGGAGGTT[A/G]AAGTGAGCTGAGATC	84628
rs6597560	snp	A/C	0.457037	0.140127	intron-variant	NTNG2	GRCh38.p7	9:132213262	GGGAGGCGGAGGTTA[A/C]AGTGAGCTGAGATCG	84628
rs6597561	snp	A/G	0.457388	0.139608	intron-variant	NTNG2	GRCh38.p7	9:132213515	ATCATTCCTCACTGC[A/G]GTCCAGGTCCCCAAC	84628
rs6597562	snp	C/T	0.492037	0.0625946	intron-variant	NTNG2	GRCh38.p7	9:132224099	ATGCCTTCTTCTTTG[C/T]ACAACCCGTGGGCTC	84628
rs7018926	snp	A/C	0.45946	0.136478	intron-variant	NTNG2	GRCh38.p7	9:132213785	GCTGGCTGTGTTAAA[A/C]TAGTAGTCTAACTTT	84628
rs7021418	snp	C/G	0.214239	0.247429	intron-variant	NTNG2	GRCh38.p7	9:132198801	GGGGTTACCTGGTAT[C/G]TGATACATCGTTACC	84628
rs7022061	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228706	gggactgcaggtgca[C/T]accaccaggcccagc	84628
rs7022336	snp	C/G	0.214239	0.247429	intron-variant	NTNG2	GRCh38.p7	9:132198822	CATCGTTACCTGGTT[C/G]CCTGGGGGTTACCTG	84628
rs7022678	snp	G/T	0.0622301	0.165053	intron-variant	NTNG2	GRCh38.p7	9:132223886	GCAGAGTAAAATCCC[G/T]CCTCCGTCTCCTGGT	84628
rs7025107	snp	A/G	0.460702	0.134554	intron-variant	NTNG2	GRCh38.p7	9:132212505	TGCCGGCCTGATTGC[A/G]TTCCAGGAGGCGCAG	84628
rs7026043	snp	A/G	0.0998734	0.199905	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230085	ggggatgctgacacc[A/G]tgcctggcacgtggg	84628
rs7026497	snp	A/G	0.487558	0.0778863	intron-variant	NTNG2	GRCh38.p7	9:132207592	catccacaaaacccc[A/G]tttccatgtaaggtc	84628
rs7026823	snp	A/T	0.499713	0.0119774	intron-variant	NTNG2	GRCh38.p7	9:132215059	attttgtgttttttt[A/T]aatttttttgtagag	84628
rs7027769	snp	C/T	0.499831	0.00918375	intron-variant	NTNG2	GRCh38.p7	9:132208484	AGGCCTGCAGGAGAC[C/T]GGGCGGGCCCTACCA	84628
rs7031109	snp	A/T	0.4776	0.103433	intron-variant	NTNG2	GRCh38.p7	9:132208728	GGGGAATTTTTTTTT[A/T]ATTTCTTAATTTTTT	84628
rs7031224	snp	G/T	0.307671	0.243257	intron-variant	NTNG2	GRCh38.p7	9:132171543	ACAGGAAAGCCAAGG[G/T]CAGGCTGTGAACGTG	84628
rs7031517	snp	A/G	0.0240643	0.107019	intron-variant	NTNG2	GRCh38.p7	9:132222458	TGCTCTATTTATTTC[A/G]GCTTGGTGTTCCAGT	84628
rs7032195	snp	C/T	0.308414	0.24308	intron-variant	NTNG2	GRCh38.p7	9:132171498	CCATGTTGGAGTCTC[C/T]AGCATACAGAGGCAC	84628
rs7036049	snp	C/T	0.0256215	0.110247	intron-variant	NTNG2	GRCh38.p7	9:132172087	GGGGAAGGAGGAGGG[C/T]GTGCCCCTCCCCATG	84628
rs7036671	snp	A/G	0.0475351	0.146656	intron-variant	NTNG2	GRCh38.p7	9:132167340	ATAGTATTCAGCTCC[A/G]CAGCCTTCAGGCTAA	84628
rs7036716	snp	C/T	0.45866	0.137698	intron-variant	NTNG2	GRCh38.p7	9:132210610	CTGGGTCTGTGGCCA[C/T]GACACCCGGCAGGCT	84628
rs7038719	snp	A/C	0.455024	0.143057	intron-variant	NTNG2	GRCh38.p7	9:132215173	agtgcccagattaca[A/C]gcatgagccactgca	84628
rs7039329	snp	C/T	0.34146	0.23267	intron-variant	NTNG2	GRCh38.p7	9:132178369	TGTTCTGTCCTCTTC[C/T]TTGTCCCACAGTCAG	84628
rs7044056	snp	A/G	0.226779	0.248919	intron-variant	NTNG2	GRCh38.p7	9:132217844	AGGCCAGTGGGGCCC[A/G]GGGGATGGGGTTACC	84628
rs7044350	snp	A/C	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132203993	aagggaGGTCCTTTG[A/C]ACCAAATTAAGGTCT	84628
rs7045357	snp	A/G	0.0154538	0.0865337	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162184	GGCGCAGCGCCGGAG[A/G]GTGGCGGTCCTCGGC	84628
rs7046069	snp	A/T	0.475525	0.107882	intron-variant	NTNG2	GRCh38.p7	9:132207263	tggagcctccataac[A/T]aagtaccactaactg	84628
rs7357745	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203215	catggtggtgtgcgc[C/T]tgtagtcctagctac	84628
rs7357747	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203410	AATGTACATGGGTAC[C/T]TATGGTACCAGCGGA	84628
rs7389445	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132218488	GCGTTTTGTtttttt[G/T]ttttttttgtttttc	84628
rs7391089	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132218487	AGCGTTTTGTttttt[G/T]gttttttttgttttt	84628
rs7849557	snp	C/G	0.297128	0.245518	intron-variant	NTNG2	GRCh38.p7	9:132205984	ATgtcagactgtcca[C/G]gtgcaaattctggat	84628
rs7850170	snp	A/G	0.316	0.241131	intron-variant	NTNG2	GRCh38.p7	9:132206508	CCTGTCTCTACTAAA[A/G]ATACAAAATTTATCC	84628
rs7850216	snp	A/T	0.464841	0.127841	intron-variant	NTNG2	GRCh38.p7	9:132189650	AGCTTAAAAAAAAtt[A/T]tttttttgagacgga	84628
rs7851167	snp	A/C	0.359575	0.224707	intron-variant	NTNG2	GRCh38.p7	9:132176555	gcataatatgccatc[A/C]tgtggacacaccata	84628
rs7851764	snp	A/G	0.263535	0.249633	intron-variant	NTNG2	GRCh38.p7	9:132185113	TCGGTGGAGGCCCCA[A/G]CCAAGGCGGGGCAGG	84628
rs7851893	snp	G/T	0.494855	0.0504572	intron-variant	NTNG2	GRCh38.p7	9:132164649	CACCGGGCACGTTCT[G/T]TCTTAGAGTTTTCTA	84628
rs7853805	snp	G/T	0.49621	0.0433651	intron-variant	NTNG2	GRCh38.p7	9:132176996	gtttttgtttttgtt[G/T]tgtgttgttttgaga	84628
rs7854265	snp	A/G	0.0256215	0.110247	intron-variant	NTNG2	GRCh38.p7	9:132170128	GCCCGGCTGCACTCC[A/G]AGGGTACAGGAGGGA	84628
rs7854536	snp	A/G	0.499477	0.0161657	intron-variant	NTNG2	GRCh38.p7	9:132170367	AGAGGATTCTTGGGC[A/G]AGGACAAAATTGCAA	84628
rs7855758	snp	C/G	0.49941	0.0171624	intron-variant	NTNG2	GRCh38.p7	9:132170598	GCGCTCTGCAAGACA[C/G]GTCTCCCGCCAGCCA	84628
rs7856706	snp	A/G	0.0539704	0.155153	intron-variant	NTNG2	GRCh38.p7	9:132182999	AGTTTGAGAAGCACC[A/G]ATTGAAACCTCTCCC	84628
rs7857072	snp	A/G	0.350764	0.228794	intron-variant	NTNG2	GRCh38.p7	9:132183292	AGGGCTGTCACGGGC[A/G]CTGCTTAATGTCAAG	84628
rs7857322	snp	A/G	0.497241	0.037038	intron-variant	NTNG2	GRCh38.p7	9:132173976	GATGGACAGACGAAC[A/G]GACAGGCAGGCAGGT	84628
rs7857828	snp	A/G	0.304937	0.243889	intron-variant	NTNG2	GRCh38.p7	9:132170682	AAAAACTAGCCACCC[A/G]AGACTCAGGGGTGAG	84628
rs7858111	snp	G/T	0.108912	0.206922	intron-variant	NTNG2	GRCh38.p7	9:132170940	AAGCCTGCCGTTGAC[G/T]AAGGGGCCAGAGGTC	84628
rs7858628	snp	C/G	0.390651	0.206682	intron-variant	NTNG2	GRCh38.p7	9:132171334	CCTCACCGACTTCCT[C/G]GGAGAGGAAACGCCT	84628
rs7864624	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189999	agcactttgggaggc[C/T]gaggcgggcggctca	84628
rs7865555	snp	A/G	0.324619	0.238604	intron-variant	NTNG2	GRCh38.p7	9:132206112	AGAGAGAGGAGCCAC[A/G]ACTGTCAGGGATACA	84628
rs7865565	snp	A/G	0.324619	0.238604	intron-variant	NTNG2	GRCh38.p7	9:132206127	AACTGTCAGGGATAC[A/G]GAGAAAGAACAGCAG	84628
rs7869433	snp	A/G	0.339429	0.233457	intron-variant	NTNG2	GRCh38.p7	9:132176821	cagcaatgtacgaga[A/G]tgccagtttctccga	84628
rs7870760	snp	A/G	0.482609	0.0916147	intron-variant	NTNG2	GRCh38.p7	9:132194717	ACCCTGAGGTTGCAT[A/G]GGGGCCTGAGGACAG	84628
rs7871414	snp	A/C	0.0395917	0.135012	intron-variant	NTNG2	GRCh38.p7	9:132234121	caacctccgcccccc[A/C]aggttcaagcaattc	84628
rs7871557	snp	C/T	0.296109	0.245711	intron-variant	NTNG2	GRCh38.p7	9:132204116	GGCATTGCATCCTCA[C/T]CCCCTTTCTGCCCAG	84628
rs7872858	snp	A/G	0.449218	0.151037	intron-variant	NTNG2	GRCh38.p7	9:132183112	TGCCTCGGCTCTCTC[A/G]GAGCCTCTCTCACAT	84628
rs7872874	snp	A/G	0.380724	0.213099	intron-variant	NTNG2	GRCh38.p7	9:132183146	AGCTGCAGGTGCTCC[A/G]TCCTCCTTCTGGCTT	84628
rs7872965	snp	C/T	0.460477	0.134905	intron-variant	NTNG2	GRCh38.p7	9:132177052	tggagtgcagtgttg[C/T]gatcttggctcactg	84628
rs7873311	snp	C/T	0.499527	0.0153681	intron-variant	NTNG2	GRCh38.p7	9:132170067	CCTTCGCCCCTTCAG[C/T]GGCAGGTGCTACGTG	84628
rs7873631	snp	G/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230480	AGCGACACCTCCAGG[G/T]GCTCCCCTGCCCTGC	84628
rs7874039	snp	C/T	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132209769	GCAAGCTTTTGAAAA[C/T]GTTTTGCTCGGAAGG	84628
rs9411447	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132163625	CCCCGGGGTGGGCTG[A/G]GTATCCCCCCTAGCC	84628
rs9696474	snp	A/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132214875	AAAATTCAAAAAAAA[A/T]TTTTTTTTTTTTTAG	84628
rs10114567	snp	C/T	0.400682	0.199487	intron-variant	NTNG2	GRCh38.p7	9:132181604	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCATAGC	84628
rs10116734	snp	A/G	0.495999	0.0445491	intron-variant	NTNG2	GRCh38.p7	9:132180304	GTGCTCCTGCCCTCC[A/G]CCAAGGCAGGCCATC	84628
rs10116759	snp	A/C	0.353154	0.227726	intron-variant	NTNG2	GRCh38.p7	9:132180427	GTGGAGAAGGCTGTT[A/C]ATCCAGAACGCACCT	84628
rs10117408	snp	C/T	0.473726	0.111565	intron-variant	NTNG2	GRCh38.p7	9:132180497	CTTTGCCCACAGTTC[C/T]GGGGCTGGCACCGTC	84628
rs10117460	snp	C/T	0.00953873	0.0683987	intron-variant	NTNG2	GRCh38.p7	9:132189749	ggttcaaatgattct[C/T]gtgcctcagcctcct	84628
rs10118240	snp	C/T	0.497668	0.0340657	intron-variant	NTNG2	GRCh38.p7	9:132181198	CAGTGATCCTCCCAC[C/T]TCAGCCTCCTGAGCA	84628
rs10119408	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132179900	GGGATCTCACTGGGC[A/G]GCCACAGAGGGGTCC	84628
rs10119807	snp	C/T	0.118584	0.212673	intron-variant	NTNG2	GRCh38.p7	9:132197708	AGCAGGGGACTAACA[C/T]CCAGCCTTCTTGGTT	84628
rs10120195	snp	A/G	0.198324	0.244601	intron-variant	NTNG2	GRCh38.p7	9:132210675	GGCCTCACCAGCTGC[A/G]ATTGGGCAGGACAGA	84628
rs10121025	snp	C/G	0.494774	0.0508504	intron-variant	NTNG2	GRCh38.p7	9:132224030	cggcaactcttgatc[C/G]tccttcaggtcttag	84628
rs10121519	snp	A/G	0.0486741	0.148216	intron-variant, missense, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237438	GTGGGCACCCCTGCC[A/G]CTGCCCCTGCCCCTG	84628
rs10123357	snp	A/G	0.0185938	0.0946107	intron-variant	NTNG2	GRCh38.p7	9:132193075	CCTGTCCCCCGCCAC[A/G]ATGCCCCCACCCCAT	84628
rs10123461	snp	A/G	0.0275645	0.114116	intron-variant	NTNG2	GRCh38.p7	9:132193553	TGCTGGGTTGATAAG[A/G]GCTTTCTGGGTAGGT	84628
rs10578395	in-del	-/GTGT			intron-variant	NTNG2	GRCh38.p7	9:132216466	TGTGTGTGTGTGTGT[-/GTGT]CCCATGGAGCGTTCT	84628
rs10594329	in-del	-/CCC	0.363359	0.222822	intron-variant	NTNG2	GRCh38.p7	9:132179000	ACTGATGAGGCACAT[-/CCC]CCCCTCTCATTTCCT	84628
rs10656671	in-del	-/A/AAA	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174921	GCAAGACTCTGTCTC[-/A/AAA]AAAAAAAAAAAGTGT	84628
rs10685870	in-del	-/GGAC	0.0221141	0.102801	intron-variant	NTNG2	GRCh38.p7	9:132173752	GCGGATGAGATGGAT[-/GGAC]GGACGGACGAACGGA	84628
rs10751490	snp	A/G	0.489492	0.0717183	intron-variant	NTNG2	GRCh38.p7	9:132186887	TGTTGGGAGTGTGGC[A/G]CAAAGGTGGGTAAGG	84628
rs10793904	snp	C/T	0.41507	0.187755	intron-variant	NTNG2	GRCh38.p7	9:132200354	ACTGCAGGCTTTCAA[C/T]GTCCACCCAAATCTG	84628
rs10901132	snp	C/T	0.245346	0.249957	intron-variant	NTNG2	GRCh38.p7	9:132164706	GGCTCTGTAACAGGT[C/T]CCCCTTTAAACAGCC	84628
rs10901133	snp	C/G	0.31503	0.241394	intron-variant	NTNG2	GRCh38.p7	9:132183278	GGCCGGCCAGCATTA[C/G]GGCTGTCACGGGCGC	84628
rs10901134	snp	A/G	0.448963	0.151372	intron-variant	NTNG2	GRCh38.p7	9:132187609	AGAGGGACAGAAAAC[A/G]AGAGGGAGGGAGGGA	84628
rs10901135	snp	C/G	0.44651	0.154543	intron-variant	NTNG2	GRCh38.p7	9:132187872	GAACACGCAGAACTT[C/G]AGACTTTAGGATGTC	84628
rs10901136	snp	A/G	0.459801	0.135955	intron-variant	NTNG2	GRCh38.p7	9:132191361	AAAATAATCGCTCCC[A/G]TTTGGAGACATTTCC	84628
rs10901137	snp	C/T	0.459574	0.136304	intron-variant	NTNG2	GRCh38.p7	9:132191372	TCCCATTTGGAGACA[C/T]TTCCTAGGGATTCTA	84628
rs10901138	snp	A/G	0.482534	0.0918038	intron-variant	NTNG2	GRCh38.p7	9:132223280	GTGGACGCAGGGGCC[A/G]CTGTTTCCCCACCCA	84628
rs10901139	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132232813	TGATCCTTCCCCCTT[G/T]GGGGGTGGCATTTCT	84628
rs10901140	snp	A/G	0.395453	0.203331	intron-variant	NTNG2	GRCh38.p7	9:132234647	GAGGACAGCGCTGCG[A/G]GCGGAAAACGCCGCT	84628
rs10901141	snp	A/G	0.467439	0.123371	intron-variant	NTNG2	GRCh38.p7	9:132235224	AGGACACTTCTGGAC[A/G]CATGTAAGATCTTGG	84628
rs11243649	snp	A/G	0.00716266	0.059414	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159989	CTGCCTGCAGGCTGA[A/G]TGCTTAAAAATCAAA	84628
rs11243650	snp	C/T	0.0402882	0.136092	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160215	ACCGTTCATATCTCA[C/T]ATATGGGGAAACTGA	84628
rs11243651	snp	A/G	0.496714	0.0404017	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162423	CTGCTACGAGCTGAG[A/G]ACTGGAGTCGCCCCA	84628
rs11243652	snp	A/G	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132164051	TCCTCCTCGTTATCC[A/G]GGGACTCCTGCCTCT	84628
rs11243653	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174107	aggccgcaccatgct[A/G]cggatgagatggaca	84628
rs11243654	snp	A/G	0.316	0.241131	intron-variant	NTNG2	GRCh38.p7	9:132183351	GGCCTTCTCTCCTGC[A/G]CTCCCCACCAAGCTC	84628
rs11243655	snp	A/T	0.495782	0.0457324	intron-variant	NTNG2	GRCh38.p7	9:132186595	CCTTGGCTTCCCAGT[A/T]GACCCTCTCCCGGGC	84628
rs11243656	snp	C/G	0.155656	0.231515	intron-variant	NTNG2	GRCh38.p7	9:132189315	CCTGGCCTCATGGGA[C/G]CTTTCATAAGGAATG	84628
rs11243657	snp	C/T	0.494609	0.0516363	intron-variant	NTNG2	GRCh38.p7	9:132189401	AGTCATGGAGAAGTA[C/T]GATTGGCTTAAAAAA	84628
rs11243658	snp	A/G	0.48155	0.0942576	intron-variant	NTNG2	GRCh38.p7	9:132189419	TTGGCTTAAAAAAAA[A/G]GTATCATCTCCTGGT	84628
rs11243659	snp	C/T	0.480461	0.0968913	intron-variant	NTNG2	GRCh38.p7	9:132190125	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	84628
rs11243660	snp	A/G	0.496616	0.0409947	intron-variant	NTNG2	GRCh38.p7	9:132190203	GCGCCACTGCACTCC[A/G]GACTGGGCGAAAGAG	84628
rs11243661	snp	A/G	0.17332	0.23795	intron-variant	NTNG2	GRCh38.p7	9:132192936	TTCCCGGGCCGGGGC[A/G]GGGGCCGGAGTGCCC	84628
rs11243662	snp	A/G	0.490343	0.0688145	intron-variant	NTNG2	GRCh38.p7	9:132196445	tgatctgcccgcctc[A/G]gcctcccaaagtgct	84628
rs11243663	snp	A/G	0.481538	0.0942867	intron-variant	NTNG2	GRCh38.p7	9:132197922	TTCCCAGGCCATCCC[A/G]AGCATCCAGCACCCA	84628
rs11243664	snp	C/G	0.483763	0.0886264	intron-variant	NTNG2	GRCh38.p7	9:132197928	GGCCATCCCGAGCAT[C/G]CAGCACCCACCCTTC	84628
rs11243667	snp	A/G	0.133435	0.221162	intron-variant	NTNG2	GRCh38.p7	9:132204711	TATGTGCATTTCCTC[A/G]TTAAGTCCTATCCTG	84628
rs11243669	snp	A/G	0.0383715	0.133092	intron-variant	NTNG2	GRCh38.p7	9:132205647	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	84628
rs11243671	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132210553	GCTGCCAACAGCGGA[C/T]GGGGGACTGAGCCCC	84628
rs11243672	snp	C/T	0.34303	0.232046	intron-variant	NTNG2	GRCh38.p7	9:132213867	GTAATAATGTGGGGA[C/T]GGGTGGTAACATACC	84628
rs11243673	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132214185	TTCCGGCAGCCAGGA[A/G]TTGACCTACATTCCA	84628
rs11243674	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132215844	GGGAGCCCATGTACT[C/T]TCATCTCCGTCCCTC	84628
rs11243675	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216513	AGAGCTAAAGCCGTA[A/G]GATTCTGCAGTGGGG	84628
rs11243676	snp	A/G	0.0349115	0.127424	intron-variant	NTNG2	GRCh38.p7	9:132221380	tgagagagccagaga[A/G]gccaagaggTCATAC	84628
rs11243679	snp	A/G	0.175897	0.238765	intron-variant	NTNG2	GRCh38.p7	9:132225519	AATTGATCCTCCTGC[A/G]TCAGCCTCCTAAAGT	84628
rs11243680	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226467	CAGGTGCTGGCAGCA[A/G]CCTCTGTCACCCATC	84628
rs11243682	snp	C/T	0.487621	0.0776941	intron-variant	NTNG2	GRCh38.p7	9:132227287	TCTACAGCTCCCAAA[C/T]GCCAGGTCTCATAAC	84628
rs11243684	snp	A/G	0.495855	0.045338	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242354	TCTTTTGTATTATCC[A/G]CCGCCCAGTTCCTTT	84628
rs11243685	snp	C/G	0.499971	0.00379382	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243590	AGAGCAGTGCCGGGG[C/G]TCCGGTCCTGGTTGC	84628
rs11243686	snp	A/G	0.174288	0.23826	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244992	ACTGTTCTTGTCTGG[A/G]GGCAAGTGGGCCACC	84628
rs11426004	in-del	-/G	0.481242	0.0950111	intron-variant	NTNG2	GRCh38.p7	9:132191558	ATGGGTATGTTAACT[-/G]CATCTTTCTTTTTTT	84628
rs11787604	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132223417	AGGACTGAGATATGA[G/T]GGAGGCCGGATGCGA	84628
rs11788572	snp	C/G	0.415727	0.187175	intron-variant	NTNG2	GRCh38.p7	9:132200650	TGTTTCACTTTGACG[C/G]TGTGTGTGGATTCCA	84628
rs11788925	snp	C/T	0.11228	0.208646	intron-variant	NTNG2	GRCh38.p7	9:132173591	CTCATTTACTGTGGG[C/T]ATAATGACAAGCTGC	84628
rs11789039	snp	C/T	0.496034	0.0443518	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243520	GCTTGGTGTCTCCAG[C/T]CCTGGGGCCACACTT	84628
rs11790939	snp	A/G	0.484561	0.0864924	intron-variant	NTNG2	GRCh38.p7	9:132188588	TGGGAGGTGGGGTTG[A/G]GGCACACAGGGCGCC	84628
rs11792556	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230089	atgctgacaccgtgc[C/G]tggcacgtgggacgc	84628
rs11792800	snp	C/T	0.417034	0.18601	intron-variant	NTNG2	GRCh38.p7	9:132195371	TGGAGCGCAGTGGCG[C/T]GATCTCGGCTTACTG	84628
rs11793404	snp	C/T	0.479824	0.098392	intron-variant	NTNG2	GRCh38.p7	9:132196550	cactgcagtattata[C/T]ggcatagcctcactg	84628
rs11794215	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232933	AAGACCTCCTCCTTC[C/T]TAGGCCATCCAGAGC	84628
rs11794640	snp	C/T	0.452965	0.145963	intron-variant	NTNG2	GRCh38.p7	9:132194109	GTTAGGGCTTCAACA[C/T]AGAAATCTGGGGGAC	84628
rs11794689	snp	C/G	0	0	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209274	cgtcttccagcgcgg[C/G]tgtgcACTGGAGGAA	84628
rs12000154	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132174186	CGGACAGGCAGGTCG[A/C]ACCATGCTGCAGATT	84628
rs12000428	snp	A/G	0.040671	0.13668	intron-variant	NTNG2	GRCh38.p7	9:132226181	tttcggttaccccga[A/G]gtacagtttatatag	84628
rs12000597	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174183	GGACGGACAGGCAGG[C/T]CGAACCATGCTGCAG	84628
rs12001245	snp	A/G	0.493703	0.0557558	intron-variant	NTNG2	GRCh38.p7	9:132208283	CCTTCTAAGGACTCA[A/G]TGTGATGTGGCTGTG	84628
rs12001942	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174036	TGGACGGACAGGCAG[A/G]CAGGCCACACCATGC	84628
rs12001961	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174168	GCGGATGAGACGGAC[A/G]GACGGACAGGCAGGT	84628
rs12002429	snp	A/G	0.0225045	0.103662	intron-variant	NTNG2	GRCh38.p7	9:132174793	cgggtgtggtggcgc[A/G]cgcctgtaatcccag	84628
rs12003562	snp	C/G	0.0387552	0.1337	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132237341	GAGCTGGCCCAGGGC[C/G]GCTCGGAAGCCTTTG	84628
rs12003603	snp	A/G	0.039522	0.134904	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237612	GCAGGATAGAGGACC[A/G]ATGCCTGGCTCCGAA	84628
rs12003622	snp	C/T	0.105924	0.204309	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229794	CTGCCAATCCCACAG[C/T]GTCCTTTCTCGGGAA	84628
rs12004211	snp	A/T	0.205417	0.245993	intron-variant	NTNG2	GRCh38.p7	9:132216191	GGTGCTCCATGCCGG[A/T]TGCTGCACACAGAGC	84628
rs12004212	snp	C/T	0.204803	0.245881	intron-variant	NTNG2	GRCh38.p7	9:132216219	AGCTCCCATGCATTA[C/T]CCCCTTCCTCCCTTG	84628
rs12004748	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132168513	GGTGATGAGGCTGTC[A/C]CTGTGGGTGGTGGCT	84628
rs12005739	snp	A/T	0.22263	0.248497	intron-variant	NTNG2	GRCh38.p7	9:132199983	TCCTGGGTCATTTGT[A/T]CTTTTGGCAGATAAT	84628
rs12005960	snp	A/G	0.187685	0.242109	intron-variant	NTNG2	GRCh38.p7	9:132195458	ggactacaggcgccc[A/G]ccaccacgcctggct	84628
rs12005962	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174163	ATGCTGCGGATGAGA[C/T]GGACGGACGGACAGG	84628
rs12236201	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211458	CTCTAGTGGTCTTCT[A/G]CTGACCTTAGACTCA	84628
rs12236995	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132228102	ATGCCAACGCCAGGG[C/T]TTAGGGCAGCTACTG	84628
rs12336280	snp	A/G	0.203267	0.245593	intron-variant	NTNG2	GRCh38.p7	9:132199062	ATATTACATCATAGG[A/G]ACTGCCTAGGATGGC	84628
rs12336310	snp	C/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132199090	GGCTGGGGCTGCACA[C/G]ACCCAATGCCTGAGC	84628
rs12340081	snp	A/G	0.277867	0.248442	intron-variant	NTNG2	GRCh38.p7	9:132235497	GTAGATTTGGACCCA[A/G]TTCCTTTGGCCAGTG	84628
rs12342696	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132173768	ggacggacgaacgga[C/G]aggcaggcaggtcga	84628
rs12342966	snp	G/T	0.421842	0.181577	intron-variant	NTNG2	GRCh38.p7	9:132241791	ACGGCGCCCCCGGGA[G/T]CTCGCACACCCTGCT	84628
rs12343811	snp	C/T	0.217551	0.247885	intron-variant	NTNG2	GRCh38.p7	9:132216731	GTCAAATTCAGAGAG[C/T]GATCGCTTGGGAAAA	84628
rs12344203	snp	A/G	0.0535932	0.154675	intron-variant	NTNG2	GRCh38.p7	9:132235358	CGGGGACGGCACAGG[A/G]AGTGTAGAAGGGTCT	84628
rs12345236	snp	A/T	0.491629	0.0641526	intron-variant	NTNG2	GRCh38.p7	9:132188705	GTGCTCCCAGCATCC[A/T]TCACCCATGAGCTGG	84628
rs12345945	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132223676	ctctgtctcaaaaca[C/T]aaaaagaTGCCGCAC	84628
rs12347450	snp	A/G	0.0448719	0.142907	intron-variant	NTNG2	GRCh38.p7	9:132182708	GAGGTTTCAGGTTTT[A/G]TGGCTCTTTTCCATC	84628
rs12348604	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132189278	AGGTTTTTTTCTGTA[A/G]AGATGGCATCTCCCT	84628
rs12348605	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132189280	GTTTTTTTCTGTAGA[A/G]ATGGCATCTCCCTGT	84628
rs12348653	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132189381	gctaggtttaatgga[A/G]aaatagtcatggaga	84628
rs12348654	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132189387	tttaatggagaaata[A/G]tcatggagaagtacg	84628
rs12348761	snp	C/T	0.0352966	0.128072	intron-variant	NTNG2	GRCh38.p7	9:132226353	TGTTGCCCTCAAGGG[C/T]GTGGCTGTGGGCCAC	84628
rs12350369	snp	C/G	0.198324	0.244601	intron-variant	NTNG2	GRCh38.p7	9:132185389	AAGCGCCCCAGCCAG[C/G]GGGGCCTGTCCCTCA	84628
rs12352286	snp	C/T	0.0941369	0.195465	intron-variant	NTNG2	GRCh38.p7	9:132174108	ggccgcaccatgctg[C/T]ggatgagatggacag	84628
rs12352564	snp	A/G	0.239902	0.249796	intron-variant	NTNG2	GRCh38.p7	9:132222610	GAGAATTCCAGAGAC[A/G]TCCTTCGTCCTGGGA	84628
rs12352825	snp	A/G	0.139225	0.224118	intron-variant	NTNG2	GRCh38.p7	9:132187183	GGAGCAGGGGCGGTC[A/G]CCGTGGCTTTGGGAG	84628
rs12378553	snp	C/T	0.492188	0.0620098	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229129	TTGAGGCCCCCAAGC[C/T]CCAGGAAGGAGGGGT	84628
rs12380847	snp	C/G	0.378174	0.214642	intron-variant	NTNG2	GRCh38.p7	9:132228454	CTCTCTTTAGTGGCC[C/G]TCACTCTCTCCCTGA	84628
rs12551018	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225699	aaatatacgttccat[G/T]tgtttgcgtgtttga	84628
rs12551583	snp	G/T	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132164861	GGGGCCCTGGCTGGG[G/T]GCTGCTCCGAGCCTG	84628
rs12682987	snp	A/C	0	0	intron-variant	NTNG2	GRCh38.p7	9:132207812	CACGGTGAGAAAGAA[A/C]CCAGGGCAAggccag	84628
rs12684040	snp	A/G	0.155325	0.23138	intron-variant	NTNG2	GRCh38.p7	9:132172831	GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC	84628
rs12684263	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132176668	ttgggtctcagtttt[C/T]gcatgtgtgtatgtc	84628
rs12685324	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132224842	GACTGCAGTTACCAA[C/T]TAGTGAATCTTCTTG	84628
rs12685984	snp	A/G	0.0923359	0.194016	intron-variant	NTNG2	GRCh38.p7	9:132184675	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG	84628
rs13283095	snp	A/G	0.271702	0.249056	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162804	CGGCCAGTCCGGCTG[A/G]AAACTTCTCCCGGCG	84628
rs13286705	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189067	AAGGCTTTAAGCCtt[C/T]ctttttttttttttt	84628
rs13286785	snp	A/G	0.00516792	0.0505693	intron-variant	NTNG2	GRCh38.p7	9:132190353	GGGGAGCTGCTGAGG[A/G]AGTGAGCCAGTGCAT	84628
rs13287944	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190371	TGAGCCAGTGCATCC[C/T]TCCACAAACCACAGA	84628
rs13290394	snp	A/C	0	0	intron-variant	NTNG2	GRCh38.p7	9:132194259	AAGTTCTTGGAGCAT[A/C]TGCCCATCACTCCTC	84628
rs13290798	snp	A/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242144	CTCCCCGCACCCGGA[A/G]gccgggggtcccggg	84628
rs13292524	snp	A/G			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242143	GCTCCCCGCAcccgg[A/G]ggccgggggtcccgg	84628
rs13293206	snp	A/G	0.499958	0.00459246	intron-variant	NTNG2	GRCh38.p7	9:132215955	CAGTGCTGAGCCCTC[A/G]AGGGTACCAGCTCAG	84628
rs13293982	snp	A/G	0.495445	0.0475058	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209090	CATTCTCCGTGGAAG[A/G]ACGTTTCGGTGGCTC	84628
rs13294775	snp	A/G	0.339429	0.233457	intron-variant	NTNG2	GRCh38.p7	9:132177223	aactcctggcctcaa[A/G]cgatctgcccgcctg	84628
rs13297136	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174095	ggacagataggcagg[C/T]cgcaccatgctgcgg	84628
rs13297139	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132174098	cagataggcaggccg[A/C]accatgctgcggatg	84628
rs13297722	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174086	cggacagacggacag[A/G]taggcaggccgcacc	84628
rs13298014	snp	C/G			utr-variant-5-prime, intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162172	CCCGAGGGGGGAGGC[C/G]CAGCGCCGGAGGGTG	84628
rs13299203	snp	C/G	0.498182	0.0300969	intron-variant	NTNG2	GRCh38.p7	9:132209860	AAAGGCGGGAGGCGC[C/G]GCAGCGTTGGCGTTG	84628
rs13301889	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174087	ggacagacggacaga[C/T]aggcaggccgcacca	84628
rs13301903	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174117	atgctgcggatgaga[C/T]ggacagacggacaga	84628
rs17148754	snp	C/T	0.0260105	0.111035	intron-variant	NTNG2	GRCh38.p7	9:132190938	TGACTTGCCTATGTG[C/T]GTCCAGAGAGATAGG	84628
rs17148762	snp	G/T	0.0441095	0.141807	intron-variant	NTNG2	GRCh38.p7	9:132193314	GTTACTGAGGTCCAG[G/T]CCCAATATGCAGGCC	84628
rs17148807	snp	A/G	0.0256215	0.110247	intron-variant	NTNG2	GRCh38.p7	9:132233965	TTGAACTCAGGGCTC[A/G]CCAACTCAGCCACCC	84628
rs17148812	snp	A/G	0.205723	0.246048	intron-variant	NTNG2	GRCh38.p7	9:132234446	ACTTGCTTCCCACAC[A/G]CCTGAGTGTGTCCCT	84628
rs17385973	snp	C/G	0.0566069	0.158427	intron-variant	NTNG2	GRCh38.p7	9:132235239	ACATGTAAGATCTTG[C/G]CCGGAACACATGTCC	84628
rs28434719	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174291	GGACAGACAGGCAGG[C/T]CGCACCATGCTGCGG	84628
rs28436026	snp	C/G	0.298651	0.24522	intron-variant	NTNG2	GRCh38.p7	9:132207995	TGTGGTCTCAGATAC[C/G]TGGGAGGCTGAGGTG	84628
rs28478381	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174250	GGCCGCACCATGCTG[C/T]GGATGAGATGGATGG	84628
rs28529868	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132188953	AGGAGAAAGATCTTT[C/T]CCTCACCCATTCTAT	84628
rs28578527	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132188952	CAGGAGAAAGATCTT[C/T]TCCTCACCCATTCTA	84628
rs28582028	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174259	ATGCTGTGGATGAGA[C/T]GGATGGATGGACAGA	84628
rs28582874	snp	A/G	0.259951	0.249802	intron-variant	NTNG2	GRCh38.p7	9:132207100	CAGCAGCACTAGGCA[A/G]AATCGGGGTTCCCTC	84628
rs28584157	snp	C/G	0.29789	0.24537	intron-variant	NTNG2	GRCh38.p7	9:132205502	GACAGCTTCAGTTTG[C/G]GATGATTTAAAGTTC	84628
rs28588863	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173712	GATGGATGGACAGAC[A/G]GACAGACAGGCAGGA	84628
rs28611196	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173718	TGGACAGACGGACAG[A/G]CAGGCAGGAGCACCA	84628
rs28668478	snp	C/G	0.498369	0.0285077	intron-variant	NTNG2	GRCh38.p7	9:132189063	GAAAAAGGCTTTAAG[C/G]CTTTCTTTTTTTTTT	84628
rs28677798	snp	A/G	0.0142736	0.0832652	intron-variant	NTNG2	GRCh38.p7	9:132187359	CTCCAGCCCTAAAAT[A/G]CCAGGTTGGTTTACG	84628
rs28758796	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132163917	GATTCTATTTGTTTC[G/T]GGGAGCTGCAGTTTC	84628
rs33967810	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132178961	GTGAGACTCGGTCTC[-/A]AAAAAAAAAAAAAAA	84628
rs34127958	in-del	-/A			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241264	GTGGGTGGGGCCTAG[-/A]TGAGAGCGGGGCAGG	84628
rs34189329	in-del	-/ACAG			intron-variant	NTNG2	GRCh38.p7	9:132174327	CGGACAGACAGACAG[-/ACAG]GTCGAACCATGCTGC	84628
rs34201249	in-del	-/CT	0.184838	0.241358	intron-variant	NTNG2	GRCh38.p7	9:132199708	AGGCAAACATGGACA[-/CT]CTTCCTAGACAGGAC	84628
rs34242909	snp	A/G	0.0314385	0.121371	intron-variant	NTNG2	GRCh38.p7	9:132206627	AGCCGAGATCGTGCC[A/G]TTGCACTCCAGCCTG	84628
rs34249367	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132200312	CTGGGGAGCCCAGCT[-/G]GGGATGATCACTGTG	84628
rs34250595	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132207990	CGCCTGTGGTCTCAG[-/T]ATACCTGGGAGGCTG	84628
rs34274493	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132179001	CTGATGAGGCACATC[-/C]CCCCCTCTCATTTCC	84628
rs34275041	in-del	-/G	0.493013	0.058691	intron-variant	NTNG2	GRCh38.p7	9:132215078	TTTTTTGTAGAGATT[-/G]GGGGGGGGGTCTCAC	84628
rs34389541	snp	C/T	0.496314	0.0427728	intron-variant	NTNG2	GRCh38.p7	9:132224015	TCTCCCCTTCTGGCC[C/T]GGCAACTCTTGATCC	84628
rs34407742	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132186709	AAGAAGACTAAGCAG[-/T]TCGATCTGCTGGAAC	84628
rs34538816	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132183249	CTCTTCACCTGTCTT[-/C]CCTGGAAGGAGGGGG	84628
rs34615380	in-del	-/A			frameshift-variant	NTNG2	GRCh38.p7	9:132227009	CGCTGCCCCATGGCT[-/A]CTCCCAACGCCTGTA	84628
rs34653212	in-del	-/T	0.498415	0.0281103	intron-variant	NTNG2	GRCh38.p7	9:132213695	GGCTCATGAAAAATG[-/T]TTTTTCCCAAAACAA	84628
rs34756571	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132191559	TGGGTATGTTAACTC[-/G]ATCTTTCTTTTTTTT	84628
rs34759051	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132163528	GCCGGCCAAGCTCCC[-/T]TTTCCCTCCCGGCAA	84628
rs34772900	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132200876	GGTGTCCAGACTTTC[-/A]AGCCCCTGGGCATCT	84628
rs34774878	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132175874	TGCCAGGTACATTCT[-/G]GGGAGTTTAGGGAAA	84628
rs34779242	in-del	-/C			frameshift-variant	NTNG2	GRCh38.p7	9:132198273	AGGACTGCATGGAGG[-/C]CTTCGGTATGTCCGC	84628
rs34795927	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132220541	CTGCAACCTCTGCCT[-/A]CCTGGGTTCAAGTGA	84628
rs34822591	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132179002	TGATGAGGCACATCC[-/C]CCCCTCTCATTTCCT	84628
rs34841916	in-del	-/A/AA	0.625	0.125	intron-variant	NTNG2	GRCh38.p7	9:132178982	TGAGACTCGGTCTCA[-/A/AA]AAAAAAAAAAAAAAA	84628
rs34910384	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132169471	TTCCCCTGGGAGGGT[-/A]CCGGGCAGTAGGATG	84628
rs34922804	snp	C/T	0.0360663	0.129354	intron-variant	NTNG2	GRCh38.p7	9:132223278	TGGTGGACGCAGGGG[C/T]CGCTGTTTCCCCACC	84628
rs34941698	in-del	-/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239988	CATCAGGGCCCTGGG[-/C]CTGGGCAAAGACCAA	84628
rs34964619	in-del	-/C			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160318	CCAAAAGCCCTGCCT[-/C]CCCCGGCCACAATCC	84628
rs34978887	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132179000	ACTGATGAGGCACAT[-/C]CCCCCCTCTCATTTC	84628
rs35040839	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132209508	AGGGGGAATCTGGCA[-/G]GGGCGGTGCCCCAAA	84628
rs35041245	in-del	-/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160446	ATGCACACAAACTGG[-/T]TTTGCATGGAGTCTG	84628
rs35184145	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161417	GCAGCCCGGCTGCGC[C/T]TGACCGGAGCCGGCT	84628
rs35185716	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132216679	GGATCAGGTGGCCCA[C/G]GTGATGGTTTTCTGG	84628
rs35217158	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132198967	TACCTGGGACACTAT[-/G]CTACTTCTTGAGATG	84628
rs35308742	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132237192	CTGATTTGCAAGCTT[-/G]GGGATGTGCTGTGTT	84628
rs35321516	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132179040	AGAAACTGAGGCCCA[A/G]AGGGTTGGAGTGACT	84628
rs35362188	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161564	TGCTCGCCGCGCCCC[-/T]TCCCCGGGCCGTGGC	84628
rs35406789	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132172722	AGGATCAGGGCTGTA[-/T]TTTTTTTTTTTTTTT	84628
rs35497672	in-del	-/A	0.344592	0.231414	intron-variant	NTNG2	GRCh38.p7	9:132176184	TCTCAAAAAAAAAAA[-/A]GTCTTATTGTGTCTA	84628
rs35579168	in-del	-/TC			intron-variant	NTNG2	GRCh38.p7	9:132216382	GCTGCTGACTCAGCC[-/TC]TCTCTCTCTCTCTCT	84628
rs35634958	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132219573	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	84628
rs35718564	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132212677	TTTGACCCAAACAGT[-/C]CCCAAGTTCTCCAGC	84628
rs35766451	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132189673	AGACGGAGTCTCACT[-/A]CTGTCACCCAGGCTG	84628
rs35812657	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132207701	CATGCTGGACACAAG[-/C]CAGGGTGCCAGGGTC	84628
rs35926851	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132204758	ATGACACAGATGAGG[-/A]AAACTGAGGCCAGGA	84628
rs36005260	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132215086	AGAGATTGGGGGGGG[C/G]GTCTCACTTTCTTGC	84628
rs36059083	in-del	-/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239981	GGAAGTCCATCAGGG[-/C]CCTGGGCCTGGGCAA	84628
rs36119694	snp	C/T	0.0221141	0.102801	intron-variant	NTNG2	GRCh38.p7	9:132195721	TGCAGCCTCAAACTC[C/T]TGGGCTCAAGCAATC	84628
rs36120935	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132163573	TGAAAGCAGATTTCA[-/C]CCCCCTCTGCCGCCC	84628
rs45462499	snp	A/C/T	0.00759729	0.0611631	intron-variant	NTNG2	GRCh38.p7	9:132239313	GAACTTGCTGGAATG[A/C/T]GTGCAGGGTGCACTG	84628
rs45538935	snp	A/G			missense	NTNG2	GRCh38.p7	9:132166935	AGGGCCCCACCTGGG[A/G]GTTCTACGCCTGCCA	84628
rs45618132	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132226765	CCCTCCTGGGCCCCT[C/T]CTGGGAGGCGCTCCT	84628
rs55679812	in-del	-/TTTTT/TTTTTTTTTTTTTT/TTTTTTTTTTTTTTT	0	0	intron-variant	NTNG2	GRCh38.p7	9:132189095	TTTTTTTTTTTTTTT[lengthTooLong]AGACAGGGTCTCACT	84628
rs55707388	snp	A/C	0.144296	0.226554	intron-variant	NTNG2	GRCh38.p7	9:132205117	GCTCCTAGGTATAGA[A/C]CCAACAGAACTGAAA	84628
rs55757425	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132206897	TGAAGAGTTGGGGGG[G/T]GGTGGGGTCCACTGC	84628
rs55780153	in-del	-/ATGTGTGTGTGTGT			intron-variant	NTNG2	GRCh38.p7	9:132216428	TCTGTGTGTGTGTGT[-/ATGTGTGTGTGTGT]GTGTGTGTGTGTGTG	84628
rs55962452	in-del	-/G	0.452719	0.146304	intron-variant	NTNG2	GRCh38.p7	9:132189419	TTGGCTTAAAAAAAA[-/G]GTATCATCTCCTGGT	84628
rs56054573	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132172082	GAGCTGGGGAAGGAG[A/G]AGGGCGTGCCCCTCC	84628
rs56076447	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132209649	AGTAGACGCACCCAG[A/G]GCAGAGCCCGGGAGT	84628
rs56128215	snp	A/G	0.0127945	0.0789527	missense	NTNG2	GRCh38.p7	9:132166965	AGCCCAAGGTGATGC[A/G]CCTGAAGGACTACGT	84628
rs56236217	snp	C/T	0.386504	0.209444	intron-variant	NTNG2	GRCh38.p7	9:132238679	GGATACCACGGCGAG[C/T]GCCGTGAACCCAGGC	84628
rs56246563	snp	G/T	0.499713	0.0119774	intron-variant	NTNG2	GRCh38.p7	9:132215490	GAGGCTGAGGCAGGA[G/T]AATTGCTTGAACCCA	84628
rs56250915	in-del	-/CCCT/T	0.487241	0.0788465	intron-variant	NTNG2	GRCh38.p7	9:132228558	TCCTTTTTTTTTTTT[-/CCCT/T]CTTAAAGATAAGTCT	84628
rs56344538	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132219589	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA	84628
rs56375258	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132205218	AACAACACAACTGTT[C/T]ATCAACAAATGAAGA	84628
rs56376087	snp	A/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132214581	AAACTTAGCTGAAAA[A/G]GTGGCTGTGGCTCTG	84628
rs56733654	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132195500	TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG	84628
rs56740978	snp	C/T	0.084364	0.187256	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244266	GTGTCACCCTCAGGA[C/T]AGTGAAGGGTGGAGC	84628
rs56783174	in-del	-/GT			intron-variant	NTNG2	GRCh38.p7	9:132174917	ACAGAGCAAGACTCT[-/GT]CTCAAAAAAAAAAAG	84628
rs57430897	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132218560	GGAGTGCAATGGCAT[A/G]ACCTCGGCCTACTGC	84628
rs57783026	in-del	-/ATGT			intron-variant	NTNG2	GRCh38.p7	9:132216428	TCTGTGTGTGTGTGT[-/ATGT]GTGTGTGTGTGTGTG	84628
rs57942639	in-del	-/AAAAA			intron-variant	NTNG2	GRCh38.p7	9:132178802	AAAAAAAAAAAAAAA[-/AAAAA]TTAGCTGGGTGTGGT	84628
rs58246041	snp	C/T	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230054	GGGTTCTTGTGAGGA[C/T]GGCACGATTTACGCA	84628
rs58477205	snp	A/G/T	0.0260944	0.111761	intron-variant	NTNG2	GRCh38.p7	9:132181110	TTTTTTTGAGACAGG[A/G/T]TCTCACTCTGTCACC	84628
rs58498935	snp	A/G/T	0.00398755	0.0445055	intron-variant	NTNG2	GRCh38.p7	9:132176507	TTTGTCCACATTGTC[A/G/T]CATGACTCAGTGCTT	84628
rs58728323	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180101	GGGTCTCTCAGGGAC[C/T]GTTTGGGCCTCTTCA	84628
rs58778331	snp	A/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174920	GAGCAAGACTCTGTC[A/T]CAAAAAAAAAAAGTG	84628
rs58804908	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132172830	TGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	84628
rs58825737	snp	C/T	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132228327	ACCCGACAGCACTCT[C/T]GGGTCTTCAAAGGCA	84628
rs58935320	snp	C/T	0.0126979	0.078662	intron-variant	NTNG2	GRCh38.p7	9:132164083	TTCCCCCTTCTCTTT[C/T]TTCTTTTTGGCAGAA	84628
rs58974463	in-del	-/AAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132190251	AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GAAGGTTTTAGGGTA	84628
rs59127784	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132220461	CTATGTTTCCTTCTT[C/T]TTTTTTTTTTTTTTT	84628
rs59132008	in-del	-/AC/CA			intron-variant	NTNG2	GRCh38.p7	9:132210901	AAGTCACACACACAC[-/AC/CA]GCAGCCATTCACTCA	84628
rs59203878	snp	A/T	0.0138799	0.0821421	intron-variant	NTNG2	GRCh38.p7	9:132172390	GTGCTGTGTGATCTC[A/T]GATGTGAGACCTAAC	84628
rs59309373	in-del	-/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132182799	CCAGGAGCGGAGCGG[-/G]CAGGGACCAGGCTGC	84628
rs59433440	snp	C/T	0.0240643	0.107019	intron-variant	NTNG2	GRCh38.p7	9:132201410	GGCAGCTTGGCTTGT[C/T]GTTGAACTCGGTTGG	84628
rs59766488	snp	C/T	0.0316868	0.121817	intron-variant	NTNG2	GRCh38.p7	9:132239009	ATGCCTTCCTCCGTC[C/T]CTGCATGACCTGGGG	84628
rs59869556	snp	A/C/T	0.000815062	0.0201709	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231336	TCGCCATCTGCTCTG[A/C/T]GAGGCAGCAGGAGAG	84628
rs59907898	snp	A/G	0.0146672	0.084371	intron-variant	NTNG2	GRCh38.p7	9:132206810	TTCCCACCAAAAAGC[A/G]GGCATGCACGATTCC	84628
rs59961455	in-del	-/AGCAAGAC			intron-variant	NTNG2	GRCh38.p7	9:132174906	CAGCCTGGGCGACAG[-/AGCAAGAC]TCTGTCTCAAAAAAA	84628
rs60030548	in-del	-/G	0.499767	0.0107802	intron-variant	NTNG2	GRCh38.p7	9:132215487	CGGGAGGCTGAGGCA[-/G]GATAATTGCTTGAAC	84628
rs60391581	snp	A/G	0.0944967	0.195752	intron-variant	NTNG2	GRCh38.p7	9:132183546	CTTCTGACTGCCCCA[A/G]CCCGTCACCTCCAGG	84628
rs60455491	in-del	-/CTCTCTCTCTGTGTGTGT			intron-variant	NTNG2	GRCh38.p7	9:132216415	TCTCTCTCTCTCTCT[-/CTCTCTCTCTGTGTGTGT]GTGTGTGTGTGTATG	84628
rs60698209	in-del	-/ATGTGTGTGTGTGTGT	0	0	intron-variant	NTNG2	GRCh38.p7	9:132216428	TCTGTGTGTGTGTGT[-/ATGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	84628
rs60721815	in-del	-/T	0.45762	0.139261	intron-variant	NTNG2	GRCh38.p7	9:132214875	AAAATTCAAAAAAAA[-/T]TTTTTTTTTTTTTAG	84628
rs60792970	snp	C/T	0.0387552	0.1337	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244368	TTATTTTTATAGAGT[C/T]GAGGTCTCACTATGT	84628
rs60859273	snp	A/G	0.0383715	0.133092	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244590	CCCTGCCTGATTGGC[A/G]TCCGGGCCCCCTGAG	84628
rs60864894	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174068	GCGGATGAGATGGAC[A/G]GACGGACAGACGGAC	84628
rs60962661	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132174921	AGCAAGACTCTGTCT[-/C]AAAAAAAAAAAGTGT	84628
rs61025145	snp	A/G	0.0383715	0.133092	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244460	GCTGAGATTACAGGC[A/G]TGAGCCACCGCACCA	84628
rs61393543	in-del	-/AAAAAAAAAAAAAA	0.120326	0.21374	intron-variant	NTNG2	GRCh38.p7	9:132213332	GTAAGACTCCATCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs61423898	snp	A/G	0.109814	0.206997	intron-variant	NTNG2	GRCh38.p7	9:132173172	CAACTCTGTCCTTAA[A/G]TCAGTTGCAAGTGAC	84628
rs61589603	in-del	-/T	0.498852	0.0239341	intron-variant	NTNG2	GRCh38.p7	9:132218488	TTTTTTGTTTTTTTT[-/T]GTTTTTCTGGTTTTT	84628
rs61611073	snp	A/C/G			intron-variant	NTNG2	GRCh38.p7	9:132191641	CAGTGGCGCGATCTC[A/C/G]GCTCACTGCAAGCTC	84628
rs61700834	snp	C/G	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132173741	GAGCACCATGCTGCG[C/G]ATGAGATGGATGGAC	84628
rs62577481	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132172748	TTTTTTTTTTTTTTG[G/T]AGTCAAAGTCTCGCT	84628
rs62577491	snp	A/T	0.206947	0.246265	intron-variant	NTNG2	GRCh38.p7	9:132188916	AGCCTCCCCTCCAAC[A/T]GAGAAGCTGAGGCTC	84628
rs62577492	snp	A/G	0.0566069	0.158427	intron-variant	NTNG2	GRCh38.p7	9:132189597	AGGGGAAGGTCAAAG[A/G]GTAACCTTCCGCTTC	84628
rs62577493	snp	A/C	0.186421	0.24178	intron-variant	NTNG2	GRCh38.p7	9:132189948	GCAACTGTGCCCAGC[A/C]TAAAATATTTTAAGA	84628
rs62577494	snp	C/T	0.408163	0.193609	intron-variant	NTNG2	GRCh38.p7	9:132190015	GAGGCGGGCGGCTCA[C/T]GAGGTCAGGAGATCG	84628
rs62577495	snp	C/G	0.496616	0.0409947	intron-variant	NTNG2	GRCh38.p7	9:132190030	TGAGGTCAGGAGATC[C/G]AGACCATCCTGGCTA	84628
rs62577496	snp	C/G	0.172674	0.237741	intron-variant	NTNG2	GRCh38.p7	9:132190441	GAGATTTCATCCCAG[C/G]GCAGGCTTGGGTGCA	84628
rs62577497	snp	C/T	0.182296	0.240658	intron-variant	NTNG2	GRCh38.p7	9:132191835	CTCAGCCTCCCAGAG[C/T]GCTTGGATTACGGGC	84628
rs62577498	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132202892	CCATGGAGATGGATG[A/C]CTGTAACCTGTTGGA	84628
rs62577520	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132221647	CCGGGACATCTTCTC[A/C]TGTTCCCGAGGAAGA	84628
rs62577521	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132228557	CCACCATCACACCCT[C/T]CTTTTTTTTTTTTCT	84628
rs62577522	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230287	CCTGTCCAGCATGTC[A/C]CCAAGGGCAAGTCAC	84628
rs62577523	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132235628	CCTCGCATAACTTGG[C/T]TTCTTCTCTTCTTCC	84628
rs62577524	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132239099	CTCCCACTTGGCCGG[C/T]CCAGACTGCGAATGC	84628
rs66498690	in-del	-/AGAG			intron-variant	NTNG2	GRCh38.p7	9:132187570	GAGCGAGAGGGAGCA[-/AGAG]AGAGAGAGAGAGAGA	84628
rs66580036	snp	A/G	0.271972	0.249033	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160632	AGGGTTAAGGTGGAG[A/G]TGAAGGGTGGCAGCA	84628
rs66630253	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132219589	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	84628
rs66661126	in-del	-/CTCTCACACA	0	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162556	ACTCTGTCTCTCTCT[-/CTCTCACACA]CACACACACACACAC	84628
rs66919296	snp	C/T	0.246769	0.249979	intron-variant	NTNG2	GRCh38.p7	9:132236898	GCGAAGGATTCACTT[C/T]GGCTGGAGCAGGAAG	84628
rs67661079	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174326	GACGGACGGACGGAC[A/G]GACAGACAGACAGGT	84628
rs71376630	in-del	-/AA	0.371987	0.218218	intron-variant	NTNG2	GRCh38.p7	9:132234027	AAAAAAAAAAAAAAA[-/AA]GATAGCTCTACCTCA	84628
rs71481386	snp	A/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132202967	CAGCTGCCTGTTGTG[A/T]GGAGTCGATGAAATG	84628
rs71482240	multinucleotide-polymorphism	AA/GC	0	0	intron-variant	NTNG2	GRCh38.p7	9:132213261	TGGGAGGCGGAGGTT[AA/GC]AGTGAGCTGAGATCG	84628
rs71501296	in-del	-/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132172737	TTTTTTTTTTTTTTT[-/T]GGAGTCAAAGTCTCG	84628
rs71501297	in-del	-/A	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132202548	CTATTTTCTCCTTCC[-/A]CACATGGGGAAACTC	84628
rs71503138	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132202679	GAGCGGGAGGGGCCT[C/T]CGCCCCCACCCTCCA	84628
rs71778231	in-del	-/GACG			intron-variant	NTNG2	GRCh38.p7	9:132173761	ATGGATGGACGGACG[-/GACG]AACGGAGAGGCAGGC	84628
rs72124353	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132178962	GTGAGACTCGGTCTC[-/A]AAAAAAAAAAAAAAA	84628
rs72546236	in-del	-/A	0.109814	0.206997	intron-variant	NTNG2	GRCh38.p7	9:132175869	CTGATTGCCAGGTAC[-/A]ATTCTGGGAGTTTAG	84628
rs72546237	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132191557	AATGGGTATGTTAAC[-/G]TCATCTTTCTTTTTT	84628
rs72763672	snp	G/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132183585	TCTGTGCCACTCATG[G/T]GGACCAGGACACAGG	84628
rs72763675	snp	C/G	0.181659	0.240478	intron-variant	NTNG2	GRCh38.p7	9:132189054	GTTTTATGTGAAAAA[C/G]GCTTTAAGCCTTTCT	84628
rs72763682	snp	C/T	0.0142736	0.0832652	intron-variant	NTNG2	GRCh38.p7	9:132194687	AGATATTGGACTCTA[C/T]GGTGAGCTCCTGCCA	84628
rs72763694	snp	A/G	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132217074	GTGCCATGCAGCCCC[A/G]AGTGCCAAGCCTGCT	84628
rs72763700	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230037	AAGGAAGTTCCCTCA[C/T]AGGGTTCTTGTGAGG	84628
rs72765806	snp	C/T	0.20111	0.245173	intron-variant	NTNG2	GRCh38.p7	9:132241600	GTGGAACAGCACGTG[C/T]ACAGCTCTGGAGACT	84628
rs73545009	snp	A/C	0.0111196	0.0737302	intron-variant	NTNG2	GRCh38.p7	9:132234523	GAAAGATCCTGAATA[A/C]CCCCGAGTGCCTCCC	84628
rs73545013	snp	C/G	0.0103295	0.0711199	intron-variant	NTNG2	GRCh38.p7	9:132234689	TCCTTTCCTGGGCTG[C/G]GCCACGGAGGATGGA	84628
rs73545016	snp	C/G	0.0209421	0.100162	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241097	AAAGGGGACGGGGCA[C/G]GACCGAGGCAGTGGG	84628
rs73559272	snp	C/G	0.0138799	0.0821421	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160250	CAAAGCAGTCTGGGC[C/G]GTGTTCCAAGTTCAC	84628
rs73559276	snp	A/G	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132163073	TGGGCGCCCTGCTCT[A/G]TGTCTTTTAATTAAG	84628
rs73559281	snp	C/T	0.0205511	0.0992634	intron-variant	NTNG2	GRCh38.p7	9:132169450	TGATGCCACAGTTTA[C/T]TGTGGCTTCCCCTGG	84628
rs73559287	snp	G/T	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132171640	GCTGCAGAGCAAATG[G/T]TTCCATTCCTCCCCC	84628
rs73561504	snp	C/T	0.240765	0.249829	intron-variant	NTNG2	GRCh38.p7	9:132177936	TGCTGGGATTACAGG[C/T]GTGAGCCACAGCGCC	84628
rs73561506	snp	C/T	0.248755	0.249997	intron-variant	NTNG2	GRCh38.p7	9:132178513	ATGTCGATAAGCATG[C/T]TACAGTGAAATTGAC	84628
rs73561511	snp	G/T	0.130008	0.219321	intron-variant	NTNG2	GRCh38.p7	9:132179846	TTCTGTCACACAGGA[G/T]TTCGAATGGTCGTTC	84628
rs73561516	snp	A/G	0.244205	0.249933	intron-variant	NTNG2	GRCh38.p7	9:132181583	GCCTCCCAAAGTGTC[A/G]GGATTACAGGCGTGA	84628
rs73561527	snp	A/G	0.00953873	0.0683987	intron-variant	NTNG2	GRCh38.p7	9:132184426	CACCCGTCATTAACC[A/G]AAGAAGCCACTGGGG	84628
rs73561537	snp	C/T	0.0197687	0.0974348	intron-variant	NTNG2	GRCh38.p7	9:132187072	GCATTTTCTGGGTCT[C/T]CTTTTGAGCCGAGGC	84628
rs73561543	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132189220	TAGCTGGGACCACTG[A/G]TGTGTGCCACCATGC	84628
rs73561547	snp	A/G	0.0225045	0.103662	intron-variant	NTNG2	GRCh38.p7	9:132189238	TGTGCCACCATGCCC[A/G]GCTAGTTTTCTTTTT	84628
rs73561561	snp	A/C	0.0310518	0.120672	intron-variant	NTNG2	GRCh38.p7	9:132193240	TGTCAATATCACTGT[A/C]ATTTTATTAATAGCT	84628
rs73561564	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132193670	ATGAAAAACTCCCAA[C/T]TCGTCTCTACCCCTC	84628
rs73561586	snp	C/G	0.206642	0.246211	intron-variant	NTNG2	GRCh38.p7	9:132201957	GTCAGAGAATAGAAG[C/G]AGATTGCACAGCGCC	84628
rs73561589	snp	C/T	0.0236746	0.106192	intron-variant	NTNG2	GRCh38.p7	9:132204376	CCTGTCCCTATTGAT[C/T]GCCCCGTAACTGGAG	84628
rs73561592	snp	A/G	0.110167	0.207236	intron-variant	NTNG2	GRCh38.p7	9:132206953	CTGCGGTCTCCTCTG[A/G]TCTTTGGCTCTGCTC	84628
rs73561596	snp	G/T	0.137242	0.225408	intron-variant	NTNG2	GRCh38.p7	9:132207744	GGGGCTGACGCTCCC[G/T]TAGTGGGAGAGCAGA	84628
rs73563327	snp	C/G	0.0501905	0.150254	intron-variant	NTNG2	GRCh38.p7	9:132223355	ACTCAGACAGGGACA[C/G]AGGCGGGACAGAGCC	84628
rs73563337	snp	A/C	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132225532	GCGTCAGCCTCCTAA[A/C]GTGCTTGGATTATAG	84628
rs73563338	snp	A/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132225562	GGTGTGCACCACCAC[A/G]CCTAGCCTGTGTGGT	84628
rs73563339	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132225591	GTTCTCTAAAAGATA[A/G]GGACTTTAAAAAACA	84628
rs73563345	snp	C/T	0.143622	0.226238	intron-variant	NTNG2	GRCh38.p7	9:132227542	CTGGGGTGTTTGGAG[C/T]GAGCCACCAAGGCCA	84628
rs73658416	snp	C/T	0.104149	0.203046	intron-variant	NTNG2	GRCh38.p7	9:132169507	AGGTAGGTCCTACTC[C/T]AATCTCATTTTTGGG	84628
rs73658417	snp	C/T	0.031825	0.122064	intron-variant	NTNG2	GRCh38.p7	9:132176376	TGCCCCTGAAAACCA[C/T]GCGTCTACTTTTTGT	84628
rs73658418	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132179594	GCCTGGGAGCCTCAT[A/G]AGTGAGAGACTGGGG	84628
rs73661554	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132188847	GTCCCTGAGGAGGGC[C/T]GGGGGCTGGGGCTGG	84628
rs73661555	snp	G/T	0.0197687	0.0974348	intron-variant	NTNG2	GRCh38.p7	9:132188874	CTGGAGTGGGGACAG[G/T]ATCAGATGTGGTCGC	84628
rs73661556	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132188887	AGGATCAGATGTGGT[C/T]GCTGCCCGCATGAAG	84628
rs73661557	snp	A/G	0.150333	0.229274	intron-variant	NTNG2	GRCh38.p7	9:132190550	TTAGTCAGGGGCCTG[A/G]AAGTTCAAATGGCTG	84628
rs73661558	snp	A/G	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132197511	AGAGTGGAAGGGCAC[A/G]TGAAGGAGACAGAAT	84628
rs73661560	snp	C/T	0.0178098	0.0926698	intron-variant	NTNG2	GRCh38.p7	9:132207196	ATGTTTTTTCTCAGA[C/T]CTTGCAGGGATGAAT	84628
rs73661561	snp	G/T	0.0178098	0.0926698	intron-variant	NTNG2	GRCh38.p7	9:132207360	TGTCCCATACCCTCC[G/T]CCCTCCGCTCGCTCC	84628
rs73661562	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132218166	CACCATGGGGGCTCC[C/T]GGCTCCTGCCACACA	84628
rs74311540	snp	A/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162535	CGTCGTGTGTGTGAG[A/T]GTGTGTGTGTGTGTG	84628
rs74311542	snp	C/T	0.182296	0.240658	intron-variant	NTNG2	GRCh38.p7	9:132189639	CAAATCCCTTCAGCT[C/T]AAAAAAAATTTTTTT	84628
rs74311544	snp	A/G	0.0383715	0.133092	intron-variant	NTNG2	GRCh38.p7	9:132206351	TGGAAAGGCAGCTTT[A/G]TGTTCTGCTTTTCAT	84628
rs74311545	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132213041	GAAGGACTTGAGGCC[A/G]GGCACAATGGCTCAT	84628
rs74329075	snp	G/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132214890	TTTTTTTTTTTTTTA[G/T]AGACAGGGTCTTGCT	84628
rs74436607	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132214889	ATTTTTTTTTTTTTT[A/G]GAGACAGGGTCTTGC	84628
rs74479112	snp	A/G	0.0444908	0.142359	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230311	AAGTCACGGCTCTGA[A/G]ATTCAGTGTCTCCTT	84628
rs74507920	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132216321	CAGAGAAGTGACTTG[C/T]TCAAGGTCACCTAGC	84628
rs74583208	snp	A/G	0.0193772	0.0965046	intron-variant	NTNG2	GRCh38.p7	9:132186130	CCCACACTCGAAGGA[A/G]GGAGCAGTGGGGTTT	84628
rs74609203	snp	A/C	0.0475351	0.146656	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244010	TGCCCAGATAAAATA[A/C]AACACCTCTCTGGGG	84628
rs74663560	snp	A/C	0.0414363	0.137845	intron-variant	NTNG2	GRCh38.p7	9:132233075	TCCTGACCCAGGAAT[A/C]CTCTTTGGGGTGGAA	84628
rs74697808	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174213	GATTAGACGGACAGA[C/T]GGACGGACGGACAGA	84628
rs74884392	snp	C/T	0.046775	0.145601	intron-variant	NTNG2	GRCh38.p7	9:132225837	TTTTTCTCCACGCAA[C/T]TCATCTGTTGGAAGA	84628
rs74897475	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132180545	GGGACGGGGCTCCCC[A/C]AGGCACTGGCTGCCA	84628
rs74901590	snp	G/T	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132195144	AATAGACTTTATATT[G/T]TAAAGCAGTTTTAGA	84628
rs74919034	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169749	GTGCTGCCGTGGTAC[A/G]TGCGGACACATAGTA	84628
rs74977400	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132218016	GTGTCACTGGTGTGC[A/G]TGGCAGCCTGTGGCA	84628
rs75026521	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220728	GCTCAGATTACAGGC[A/G]TGAGCCACCGCACCT	84628
rs75165660	snp	A/G	0.0693013	0.172766	intron-variant	NTNG2	GRCh38.p7	9:132173131	TTCTGTGGGATTTGC[A/G]ATTGGATGAAGCCGG	84628
rs75178389	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132218497	TTTTTTGTTTTTTTT[G/T]TTTTTCTGGTTTTTT	84628
rs75182564	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132206832	CACGATTCCAGACCA[C/T]ATCAGCCTCCACTGA	84628
rs75287598	snp	G/T	0.13446	0.221699	intron-variant	NTNG2	GRCh38.p7	9:132174364	TGCTGCAGATTAGAC[G/T]GACAGATGGACGGAC	84628
rs75344539	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132167164	TGACTTTCCTGCCTC[C/T]TGACCAGGTCTGGAC	84628
rs75350912	snp	C/T	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132180131	AGCCCCTCATTCCAC[C/T]TCCCTCCTGCTGCCC	84628
rs75389653	snp	A/C	0.0349115	0.127424	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159923	CAGGCTGAGGGCTGA[A/C]CCTGGTCATCACTCA	84628
rs75398539	snp	A/G	0.0391387	0.134304	intron-variant	NTNG2	GRCh38.p7	9:132194886	AGTGGCACCTGGTGG[A/G]GGCCGCGGGGCTGTG	84628
rs75484669	snp	C/T	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132217654	AATGGAAAACTGGCA[C/T]GTCCTAGGCACCTGT	84628
rs75499113	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132214866	AAAATTCAAAAAAAA[-/A]TTTTTTTTTTTTTTA	84628
rs75549237	snp	C/G	0.0722614	0.17581	intron-variant	NTNG2	GRCh38.p7	9:132176198	TCAAAAAAAAAAAGT[C/G]TTATTGTGTCTAACA	84628
rs75552581	snp	C/G	0.499982	0.00299515	intron-variant	NTNG2	GRCh38.p7	9:132241724	CCGTCACCCTCCGAG[C/G]GGGGACGTTTCGCAC	84628
rs75595485	in-del	-/AGCAAGACTCTG			intron-variant	NTNG2	GRCh38.p7	9:132174906	CAGCCTGGGCGACAG[-/AGCAAGACTCTG]TCTCAAAAAAAAAAA	84628
rs75619469	snp	C/G	0.040671	0.13668	intron-variant	NTNG2	GRCh38.p7	9:132238329	GAGCTGGTTAGGCAG[C/G]GGTCAGCCTGAGAAC	84628
rs75624134	snp	A/T	0.155325	0.23138	intron-variant	NTNG2	GRCh38.p7	9:132203391	AAAATAATGAGAAGA[A/T]GATAATGTACATGGG	84628
rs75645195	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174218	GACGGACAGATGGAC[A/G]GACGGACAGACAGGC	84628
rs75767547	snp	A/G	0.0383715	0.133092	intron-variant	NTNG2	GRCh38.p7	9:132206195	TGGGCTCTTAGGAGC[A/G]CAAAGGGTGGGTTTC	84628
rs75804539	snp	C/T	0.0178098	0.0926698	intron-variant	NTNG2	GRCh38.p7	9:132236013	AAGCCCTTCCACCAG[C/T]ACTCCCTCCGAGGGC	84628
rs75846942	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176907	TAGTGGGTGTGGGGC[A/C]GTATCCCATTATGGT	84628
rs75993251	snp	C/T	0	0	utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242403	TCTTTTTTTTTTTTT[C/T]TTTCTGGCGGTGAGC	84628
rs76093492	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132219221	ACTCTGTCTCAAAAC[A/C]AAAAAAAAAAAGAAA	84628
rs76117950	snp	A/C	0.0142736	0.0832652	intron-variant	NTNG2	GRCh38.p7	9:132211223	CTCTGTGGGACAAAG[A/C]CCCCTCTGGGCTTCT	84628
rs76163313	snp	A/C	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174294	CAGACAGGCAGGCCG[A/C]ACCATGCTGCGGATG	84628
rs76167364	snp	C/T	0.0168055	0.0901129	intron-variant	NTNG2	GRCh38.p7	9:132219645	ATCACTGACCGCTTT[C/T]ACTTGGCATAATGTT	84628
rs76219920	snp	C/T	0.0205511	0.0992634	intron-variant	NTNG2	GRCh38.p7	9:132165945	GCTTTTGTTCTTATA[C/T]GTCTCTATTCTCCCC	84628
rs76228868	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132216414	TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTAT	84628
rs76379008	snp	A/G	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132178544	TGCGCCCAGGAAAGG[A/G]GACCCCAGAAGCAGG	84628
rs76420183	snp	A/G	0.0379877	0.132479	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244470	CAGGCATGAGCCACC[A/G]CACCACCTGCCTGTC	84628
rs76429605	snp	C/T	0.106987	0.205054	intron-variant	NTNG2	GRCh38.p7	9:132169192	CTCCACAATCTCCCA[C/T]ATGGGCAAGTCCTCG	84628
rs76435972	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240749	TGGCCACCCTGGGAA[C/G]TCCCCACCTGCCGTC	84628
rs76473820	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174205	ATGCTGCAGATTAGA[C/T]GGACAGATGGACGGA	84628
rs76504806	snp	G/T	0.156319	0.231784	intron-variant	NTNG2	GRCh38.p7	9:132206777	CAACTGCATCTCCCA[G/T]GCCCCCTGAGCTACT	84628
rs76522262	snp	C/T	0.0260105	0.111035	intron-variant	NTNG2	GRCh38.p7	9:132190726	GGAAAAGCATTTAAG[C/T]GCCCATGACGAGGCT	84628
rs76533982	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132227236	GCATGCACAGAAACA[C/T]ACGTGCGTGCATGCA	84628
rs76739721	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185614	TGGGCTTCTCCGGAT[A/G]TAGCCCTCTTCCTCT	84628
rs76970852	snp	A/G	0.0876345	0.190099	intron-variant	NTNG2	GRCh38.p7	9:132186827	CTGCAGAGGGTCCTC[A/G]CTCAGTTAGGGAATG	84628
rs77142518	snp	C/T	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132191331	GTCCCTGAGTTAATA[C/T]GAAGCTGCTGTTTCA	84628
rs77167716	snp	A/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132189421	GGCTTAAAAAAAAGG[A/T]ATCATCTCCTGGTGA	84628
rs77177867	snp	C/T	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132188313	TTGGCAAATCAGCAA[C/T]AGCAGTCAAGAGACG	84628
rs77210816	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132174280	GATGGACAGACGGAC[A/G]GACAGGCAGGCCGCA	84628
rs77271636	snp	A/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132214888	AATTTTTTTTTTTTT[A/T]AGAGACAGGGTCTTG	84628
rs77306622	snp	G/T	0.0414363	0.137845	intron-variant	NTNG2	GRCh38.p7	9:132233139	ACATAGGTTGGCCCA[G/T]CCACAAGGGACCTGT	84628
rs77347354	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132185613	CTGGGCTTCTCCGGA[A/T]GTAGCCCTCTTCCTC	84628
rs77492994	snp	G/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132173121	GCAGTCCCTGTTCTG[G/T]GGGATTTGCGATTGG	84628
rs77615439	in-del	-/CAAAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213331	AGTAAGACTCCATCT[-/CAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs77622207	snp	C/T	0.154993	0.231244	intron-variant	NTNG2	GRCh38.p7	9:132204844	ACTTTGGGAGGCTGA[C/T]GCAGGAGGATCTCTT	84628
rs77636141	snp	A/G	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132189608	AAAGAGTAACCTTCC[A/G]CTTCTGTGGTTTTCT	84628
rs77683467	snp	A/G	0.0146672	0.084371	intron-variant	NTNG2	GRCh38.p7	9:132177472	TTTGAGTTAATTTTT[A/G]TATCTGGTGTAAGGG	84628
rs77832141	snp	C/T	0.0532157	0.154195	intron-variant	NTNG2	GRCh38.p7	9:132187899	TGTCAGGGTCAGAGG[C/T]GGACAGCCCACTCCT	84628
rs77858664	snp	A/G	0.0577344	0.159793	intron-variant	NTNG2	GRCh38.p7	9:132169706	ATGTAGGAGTGTCAC[A/G]GTGCTGGCGGGACGG	84628
rs77874701	snp	C/G	0.0236746	0.106192	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166409	GAGCCCTTTAAAGAC[C/G]TGGATTGATTGGAAG	84628
rs77920123	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216661	GAAAAGTGCTGTGTC[A/G/T]GGGGATCAGGTGGCC	84628
rs77958310	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132210910	CAAGTCACACACACA[-/AC]CGCAGCCATTCACTC	84628
rs78077412	snp	A/C	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174344	CAGACAGACAGGTCG[A/C]ACCATGCTGCAGATT	84628
rs78160815	snp	G/T	0.0178098	0.0926698	intron-variant	NTNG2	GRCh38.p7	9:132174309	CACCATGCTGCGGAT[G/T]AGACGGACGGACGGA	84628
rs78187358	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235765	GAGACCCCGGGGAAG[C/T]GCCCTCTTAGACTCG	84628
rs78202140	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132228571	TCCTTTTTTTTTTTT[C/T]TTAAAGATAAGTCTC	84628
rs78218984	snp	A/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132208638	GGAGGACTCCCAGGC[A/G]TCTGGCTTTGAGACA	84628
rs78219649	snp	A/G	0.0298908	0.118541	intron-variant	NTNG2	GRCh38.p7	9:132201865	CCAGACCTGATCCCC[A/G]CCCCCTGGAGCGCTC	84628
rs78236014	snp	A/G	0.0995161	0.199636	intron-variant	NTNG2	GRCh38.p7	9:132167950	TCTGTTCTGTCATCT[A/G]CAAAATGGGCACACT	84628
rs78237972	snp	C/T	0.24932	0.249999	intron-variant	NTNG2	GRCh38.p7	9:132180449	AACGCACCTTGTCTC[C/T]GCCCCTGTCCCCACC	84628
rs78252057	snp	C/T	0.0142736	0.0832652	intron-variant	NTNG2	GRCh38.p7	9:132206194	ATGGGCTCTTAGGAG[C/T]GCAAAGGGTGGGTTT	84628
rs78324386	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132219574	CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAG	84628
rs78478439	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132169741	GCCCGGCCGTGCTGC[C/T]GTGGTACGTGCGGAC	84628
rs78497347	snp	C/T	0.0372196	0.131242	intron-variant	NTNG2	GRCh38.p7	9:132234588	CTGGGCCTCTGAACT[C/T]CTGGGCCAGATGTTT	84628
rs78529166	snp	A/G	0.0391387	0.134304	intron-variant	NTNG2	GRCh38.p7	9:132206919	GTCCACTGCCAAGGC[A/G]GGTGGTTGACCCCTG	84628
rs78633999	snp	C/G	0.0429648	0.14013	intron-variant	NTNG2	GRCh38.p7	9:132233350	ACACACACACACACA[C/G]AGGAATCCATTTGCA	84628
rs78634871	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216189	CAGGTGCTCCATGCC[A/G]GTTGCTGCACACAGA	84628
rs78674607	snp	G/T	0.0399052	0.1355	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161007	ACACCTGCCTCCCAT[G/T]CTTGCAGGGGAGGGA	84628
rs78716473	snp	A/G	0.0205511	0.0992634	intron-variant	NTNG2	GRCh38.p7	9:132188895	ATGTGGTCGCTGCCC[A/G]CATGAAGCCTCCCCT	84628
rs78765126	snp	A/G	0.0158469	0.0875917	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160933	AGCCCAGGGCTGCCG[A/G]ATATGATATTGTGAA	84628
rs78821118	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132185615	GGGCTTCTCCGGATG[G/T]AGCCCTCTTCCTCTC	84628
rs78901528	snp	A/G	0.0279526	0.114869	intron-variant	NTNG2	GRCh38.p7	9:132225656	TAGTATCTAATATAG[A/G]CAATGTCCAAATTTC	84628
rs78995714	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174336	CGGACGGACAGACAG[A/G]CAGGTCGAACCATGC	84628
rs79014929	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232641	GGAAGACGATGACCA[A/G]GGGGAATTCTTCCTG	84628
rs79068110	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132219965	TCCCACCAGCAGCGT[A/C]TGAGGGTTCTGATTT	84628
rs79125289	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132221909	GTTATCACCCAAAGT[C/T]GATGGCAATCTTTTC	84628
rs79141471	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132165959	ACGTCTCTATTCTCC[C/T]CCTCTTTAATTTGTT	84628
rs79179792	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132168724	CCACATCTCAAAGCC[A/G]GTGGGAGGGTTCTCC	84628
rs79232328	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132169482	AGGGTCCGGGCAGTA[A/G]GATGCTCTGAGGTAG	84628
rs79314968	snp	A/G	0.0150606	0.0854603	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209147	CTGCTATAAACATTC[A/G]TGGAAAGGTTTTTGG	84628
rs79328481	snp	C/T	0.040671	0.13668	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237861	CACGGGTCACCGATG[C/T]TGCTCTTTGGGACAC	84628
rs79334956	snp	G/T	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132232852	GAGTCCCCTCCATCA[G/T]CTCCTGCCTCGGCCT	84628
rs79414244	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132205652	TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG	84628
rs79541714	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160607	TTTTCAGGGCAGCTG[A/G]GAACAGGGAAGGGTT	84628
rs79585837	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220136	GCCATTTGTATGCCT[C/T]CTTCGGAGAAATGTC	84628
rs79607503	snp	A/G	0.0174175	0.0916809	intron-variant	NTNG2	GRCh38.p7	9:132227155	CACATGCATGCAAAC[A/G]TGCACACAGAAACAT	84628
rs79673784	snp	C/G	0.0298908	0.118541	intron-variant	NTNG2	GRCh38.p7	9:132207371	CTCCGCCCTCCGCTC[C/G]CTCCTGGTGGGGCCG	84628
rs79688304	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132228559	ACCATCACACCCTCC[C/T]TTTTTTTTTTTCTTA	84628
rs79777304	snp	C/T	0.0391387	0.134304	intron-variant	NTNG2	GRCh38.p7	9:132207007	GCAGGAGGGGCATCT[C/T]GGCCTTGGCCAGGGT	84628
rs79810606	snp	A/G	0.0356815	0.128715	intron-variant	NTNG2	GRCh38.p7	9:132194349	TGCTGGCTCCCTCAC[A/G]GGTCAAGCCTGCCTC	84628
rs79867980	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132174376	GACGGACAGATGGAC[A/G]GACGGACAGACAGGC	84628
rs79903499	snp	C/T	0.046775	0.145601	intron-variant	NTNG2	GRCh38.p7	9:132225877	TTACTGCCGGAGTTT[C/T]CTCGAGTCCAGATCT	84628
rs79951807	snp	C/G	0.0372196	0.131242	intron-variant	NTNG2	GRCh38.p7	9:132211653	GCAAACTCCTCACCC[C/G]TCAGGACTTGGCTCA	84628
rs80099439	snp	C/T	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132188374	TGCGGGAGCACAGTG[C/T]GGCCCAGGCAACAGC	84628
rs80245995	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132233881	AATTACACCTCAATC[-/A]AGCTGTTTCAGAAGA	84628
rs80257007	snp	G/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132189420	TGGCTTAAAAAAAAG[G/T]TATCATCTCCTGGTG	84628
rs80284748	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174922	GCAAGACTCTGTCTC[A/C]AAAAAAAAAAGTGTA	84628
rs80349289	snp	C/T	0.00438332	0.0466095	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209178	GTGAACATAAGTTTT[C/T]GCTTCTCTTGGGTAA	84628
rs80349554	snp	A/G	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132185894	AGGAGGAGGAGGAGG[A/G]AAAGGAGGAGGAGCA	84628
rs80354363	snp	A/G	0.0248432	0.108648	intron-variant	NTNG2	GRCh38.p7	9:132174305	GCCGCACCATGCTGC[A/G]GATGAGACGGACGGA	84628
rs111229390	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174079	GGACAGACGGACAGA[C/T]GGACAGATAGGCAGG	84628
rs111311281	in-del	-/ATATA	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132165296	CTGGTATCTATTTTG[-/ATATA]ATATATTAATTATAT	84628
rs111353478	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185843	AGGAGGAGGAGTGGG[A/G]GGAGGAGGAGGAGTG	84628
rs111364952	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132209784	CGTTTTGCTCGGAAG[A/G]GGAGCAGAGAGATGG	84628
rs111367038	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132238682	TACCACGGCGAGCGC[C/T]GTGAACCCAGGCGTC	84628
rs111369550	snp	C/G/T	0.0391387	0.134304	intron-variant	NTNG2	GRCh38.p7	9:132206941	TGACCCCTGGACCTG[C/G/T]GGTCTCCTCTGGTCT	84628
rs111376316	in-del	-/C	0.198152	0.244565	intron-variant	NTNG2	GRCh38.p7	9:132212932	ACACATCTCTCCCAA[-/C]CCCCCAAAGAAGACC	84628
rs111440292	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172804	GCGCAATCTCGGCTC[A/G]CTGCAAGCTCTGCCT	84628
rs111477411	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132213182	TAAAAATTAGCCAAG[C/T]ATAGTGGTGCATGCC	84628
rs111490570	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132182846	CTGGCTCTCAGCCGG[A/G]GTGCACACTGGACTT	84628
rs111512381	snp	A/C	0.00318978	0.0398085	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244667	AGCCCCCCATGGTGA[A/C]CCTCAAGTCACCAGG	84628
rs111585739	snp	A/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132205609	AAGGTGGCTGGGCGC[A/G]GTGGCTCATGCCTGT	84628
rs111593279	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222972	AAATGAAATTAGCCA[A/G]GCATGGTGGCACGCG	84628
rs111641477	snp	C/T	0.021333	0.101051	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243591	GAGCAGTGCCGGGGG[C/T]CCGGTCCTGGTTGCT	84628
rs111657772	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132174449	GAGGAGATGGGGCCC[A/G]GGGGCATCCCGCACT	84628
rs111664024	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132227634	TTATCCCTTTTTACA[G/T]ATGTGTCCTCTACGG	84628
rs111674971	snp	C/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132176378	CCCCTGAAAACCACG[C/T]GTCTACTTTTTGTCT	84628
rs111767695	snp	C/T	0.0185938	0.0946107	intron-variant	NTNG2	GRCh38.p7	9:132219894	CTGGGCAACTCTAAG[C/T]TCACCTTTTGTAGAA	84628
rs111792420	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132227950	TTGGTGTCCGAGGCC[C/T]TCCTAGGCACTTTGT	84628
rs111799027	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132201970	AGGAGATTGCACAGC[A/G]CCACTACATGGCAGA	84628
rs111812007	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132177782	CCTGCCTCAGCCTCC[A/C]AAGCAGCTGGGATTA	84628
rs111814862	snp	A/G	0.0260105	0.111035	intron-variant	NTNG2	GRCh38.p7	9:132174143	ACAGATAGGCAGGCC[A/G]CACCATGCTGCGGAT	84628
rs111839214	in-del	-/G	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132208133	TATGGGAGTGGAGCT[-/G]GGAACCAACCTGAGA	84628
rs111867590	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132181864	CCTCCAGCCTGGGCC[A/G]CCCGGCCCGGCATCC	84628
rs111906813	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162554	TGTGTGTGTGTGTGT[C/G]TGAGAGAGAGACAGA	84628
rs112008635	snp	C/G	0.0217236	0.101931	intron-variant	NTNG2	GRCh38.p7	9:132194897	GTGGGGGCCGCGGGG[C/G]TGTGGCTCAGCCCCT	84628
rs112009650	snp	A/G	0.00636936	0.0560724	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132208827	TAGAGTCATGCAACC[A/G]CCACCACAGCCTGGG	84628
rs112019926	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132183539	AGGAAGCCTTCTGAC[C/T]GCCCCAGCCCGTCAC	84628
rs112033029	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132188844	CGAGTCCCTGAGGAG[A/G]GCCGGGGGCTGGGGC	84628
rs112047778	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132192399	AGTTCGAGACCAGCC[C/T]TGCCAACATGGTGAA	84628
rs112096623	snp	C/T	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132234113	GCTCACTGCAACCTC[C/T]GCCCCCCCAGGTTCA	84628
rs112098076	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132212335	CTCCCAGCACCCGCC[C/T]GTCAGCCTCTGTGTT	84628
rs112105333	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132234811	TCCCACTGAACATCA[C/T]ATTAAAGTCAATTCA	84628
rs112148561	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132218667	ACACCCAGCTAATTT[C/T]TGTATTTTTAGTAGA	84628
rs112168068	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207745	GGGCTGACGCTCCCG[G/T]AGTGGGAGAGCAGAA	84628
rs112170038	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173681	AGGCAGGCCGCACCA[C/T]GCTGCGGATGAGACG	84628
rs112179857	in-del	-/GTGTGAGA	0.5	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162555	TGTGTGTGTGTGTGT[-/GTGTGAGA]GAGAGAGAGACAGAG	84628
rs112181461	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240609	AGATGGGAAGGACAG[A/C]GACCCCTCTAGTTGC	84628
rs112184549	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177481	ATTTTTGTATCTGGT[A/G]TAAGGGAAAAGGTCT	84628
rs112194309	snp	A/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132227253	CGTGCGTGCATGCAC[A/C]CCCACACACACACCT	84628
rs112199332	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244317	CCTGGGACACCTGCC[C/T]TGGCTGCAACCTCTG	84628
rs112218448	snp	A/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132172899	CACGCCAGGCTAATT[A/T]TTTGTATTTTTAGTA	84628
rs112243150	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132189787	TGGGACTACAGGCAC[A/G]AAACGCTATGCCCAA	84628
rs112244926	snp	C/G	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132219889	AATTACTGGGCAACT[C/G]TAAGTTCACCTTTTG	84628
rs112292574	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239936	GCTTTCTTCCAAGTT[C/T]TACTCAAGGACTGGC	84628
rs112308607	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132175961	GGGTCCTAGATGTAT[A/G]CCCCGGGCTCAGCAT	84628
rs112339809	in-del	-/C	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132182089	TGACGGTGTTCCCCA[-/C]CCCCTGCCCTTTGAG	84628
rs112346096	snp	C/T	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132205655	GGAGGCCGAGGCGGG[C/T]GGATCACTTGAGGTC	84628
rs112401031	snp	C/G	0.0360663	0.129354	intron-variant	NTNG2	GRCh38.p7	9:132174578	GTGTACAAATAAGAC[C/G]AGACCAGGCGTGTGA	84628
rs112404441	snp	C/T	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132203428	TGGTACCAGCGGAAG[C/T]GATAGGGAAGGGTGT	84628
rs112422870	snp	A/G	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132218349	TGACATGTCATTCAG[A/G]GGATTGCTGTGAAGG	84628
rs112471944	snp	C/T	0.0607341	0.163335	utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242355	CTTTTGTATTATCCG[C/T]CGCCCAGTTCCTTTT	84628
rs112505084	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132183757	AGTGTCATCGTGTGG[A/G]GGCCCTTCCCTGGAC	84628
rs112554179	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207398	GCCGGCAGCCTCTGG[A/C]GTTCCTGGGCTTGCA	84628
rs112555519	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221102	TCATGATGAGTTTTA[C/T]GGGGAGGGAGAGTGT	84628
rs112597656	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230958	CCTCCTGCCACCCAC[A/G]CCACTTCTCTCACCT	84628
rs112615507	snp	A/C	0.0166325	0.0896639	intron-variant	NTNG2	GRCh38.p7	9:132178207	CCCCTCCCCACCCTC[A/C]TTTTCTTCTCCCTCT	84628
rs112636665	snp	C/G	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132205448	ATGGTGGCTGCCAGG[C/G]GCTGGGGGAAGGCGG	84628
rs112636911	snp	C/T	0.0524604	0.153226	intron-variant	NTNG2	GRCh38.p7	9:132205602	CAATGGTAAGGTGGC[C/T]GGGCGCGGTGGCTCA	84628
rs112706120	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132207937	GGTGAAACCCCATCA[C/T]GACAAAAAATACAAA	84628
rs112753487	snp	A/C/G	0.0352966	0.128072	intron-variant	NTNG2	GRCh38.p7	9:132173145	CGATTGGATGAAGCC[A/C/G]GGAGGTTTGCACAAC	84628
rs112765705	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167924	CTCTGGCCCAGTGAC[A/G]TCTGTGGGCTTCTGT	84628
rs112813443	snp	G/T	0.0228947	0.104514	intron-variant	NTNG2	GRCh38.p7	9:132218161	ACCAGCACCATGGGG[G/T]CTCCCGGCTCCTGCC	84628
rs112862110	snp	G/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132171691	GAATGCAGACAGCAG[G/T]CAGGTCCTGGAGTCC	84628
rs112933386	snp	A/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132215853	TGTACTCTCATCTCC[A/G]TCCCTCCCTCTATCA	84628
rs112948756	snp	A/G	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132215710	TATCTCTATTTTGGG[A/G]AGCTGCAGGCTCTGA	84628
rs112969702	snp	G/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132165132	TCATGCAGGCACTTT[G/T]TTACTGCAGTAACCT	84628
rs112976119	snp	A/G	0.0509478	0.151255	intron-variant	NTNG2	GRCh38.p7	9:132186223	CCTTACCCTGTCTGA[A/G]ACAGACGCCCATGTG	84628
rs112978044	snp	C/G	0.00274441	0.0369415	intron-variant	NTNG2	GRCh38.p7	9:132197958	CCCTTCTCCTCTCCC[C/G]GCTGCAGGAGAATCC	84628
rs112989741	snp	G/T	0.00279162	0.0372561	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244366	ACTTATTTTTATAGA[G/T]TTGAGGTCTCACTAT	84628
rs112998305	snp	A/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162553	GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGACAG	84628
rs113043492	snp	A/G	0.0185938	0.0946107	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209037	TCACTCCTGAGTAGG[A/G]CTGTGCCGTGTGCAC	84628
rs113049267	snp	C/T	0.0387552	0.1337	intron-variant	NTNG2	GRCh38.p7	9:132174071	GATGAGATGGACAGA[C/T]GGACAGACGGACAGA	84628
rs113066981	in-del	-/AGAGAG	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132187570	GAGCGAGAGGGAGCA[-/AGAGAG]AGAGAGAGAGAGAGA	84628
rs113091534	snp	A/C/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132170801	CCTCAGTGCAGCAGC[A/C/G]CTGACCTCACCTTGA	84628
rs113122001	snp	A/G	1.68869e-05	0.00290571	intron-variant	NTNG2	GRCh38.p7	9:132239314	AACTTGCTGGAATGC[A/G]TGCAGGGTGCACTGC	84628
rs113131636	snp	A/C	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132218448	CTGTCTACCCAGGAG[A/C]CTTCCTTTGAGGCAC	84628
rs113134981	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132223661	GGTGACAGAGTGAGA[C/T]TCTGTCTCAAAACAC	84628
rs113271815	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132215389	AGTTTGAGACCAGCC[C/T]GGCCAACGTGGTGAA	84628
rs113346963	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132215049	GCCCTGATAAATTTT[A/G]TGTTTTTTTTAATTT	84628
rs113368492	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132224644	ATTTTAATAAAAATA[A/G]GATTCTACTAAACCC	84628
rs113379138	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132224827	GTGTACCTCTCACCC[A/G]ACTGCAGTTACCAAC	84628
rs113412096	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132218176	GCTCCCGGCTCCTGC[C/T]ACACAGGCCACCCGG	84628
rs113433484	in-del	-/TTTG	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132177650	AAATCTCTGGGTTTT[-/TTTG]TTTGTTTGTTTGTTT	84628
rs113531111	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230167	GCCACACTGCACTTC[G/T]TAGACAGGAACACTC	84628
rs113531290	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162555	GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACAGAG	84628
rs113554964	snp	G/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132175289	GGGTTCAGCCTTCCT[G/T]TGTCTGGCTCCTGAC	84628
rs113561230	snp	C/T	0.5	0	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166616	TCTGTCCATCAGCAG[C/T]CTGAGAAACGCTGGC	84628
rs113562113	snp	C/T	0.5	0	utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242649	GAGGCCCGGTGACCA[C/T]GGAACTCACCGTCTG	84628
rs113587823	snp	C/G	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132185408	GCCTGTCCCTCACCC[C/G]ACCCCGGCACTGAAA	84628
rs113597308	in-del	-/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132215088	TTTTTTGTAGAGATT[-/G]GGGGGGGGGGTCTCA	84628
rs113624691	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196780	CTGCCCAGAGCTGGC[A/G]TCAGAACCCTCAGGT	84628
rs113664916	snp	C/T	0.00279162	0.0372561	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244798	CCAGAGAAACAGCAG[C/T]GCTGGCCGCAGTCGG	84628
rs113669887	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132218988	AGCGTACAATTCAGT[C/T]GCTTTTAGGTTATTC	84628
rs113704907	snp	C/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132172205	TTCTACCTGGATAAC[C/G]CTGGCTCCTTTTTCA	84628
rs113722258	snp	A/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132217605	TGTTGAAAGCTCTGA[A/G]GATCCCTGGCTCTAG	84628
rs113725241	snp	C/G	0.0217236	0.101931	intron-variant	NTNG2	GRCh38.p7	9:132236195	TGGTGGGTGAAGGGA[C/G]AAGGCAGCACATTCC	84628
rs113770003	snp	C/T	0.00246681	0.0350331	intron-variant	NTNG2	GRCh38.p7	9:132226846	CTCTCGGTGTCTCCC[C/T]AGGTGCAAGTGCAAC	84628
rs113801437	snp	C/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132235611	TTCCCTCAGCACCAC[C/T]CCCTCGCATAACTTG	84628
rs113807683	snp	C/T	0.0524604	0.153226	intron-variant	NTNG2	GRCh38.p7	9:132182558	TGGAGGCAGCAGCCA[C/T]GACCTTGGGTGGACG	84628
rs113820976	snp	A/G	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132168695	GAAGGCCAGGATAGG[A/G]GCTGGTACTCAGTCC	84628
rs113823130	snp	A/G	0.117886	0.21224	intron-variant	NTNG2	GRCh38.p7	9:132236171	CATGAGACCTCGGAG[A/G]GTGGACTGTGGTGGG	84628
rs113838370	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195801	GCCCAGCTAATTTTT[A/T]AATTTTTTTTTGTAG	84628
rs113861354	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132167491	ATCCAATCCAGCAGA[C/T]GGTACCATGAAGCTA	84628
rs113869694	snp	C/T	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132212345	CCGCCCGTCAGCCTC[C/T]GTGTTGTGTGCAAGG	84628
rs113872829	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132241552	CAAGTCGGCGTTAGC[C/G]GCGGGCACAGGGTGA	84628
rs113880896	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132195501	TTTTTTTTTTTTTTT[A/G]TATTTTTAGTAGAGA	84628
rs113889802	snp	C/T	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132218880	AAAGCCTGGAAGCTG[C/T]AAGCCCTTCCCTGTT	84628
rs113904636	snp	A/T	0.0209421	0.100162	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132237287	AGAGGGGCCTCTCCC[A/T]CCCTCACATCTGAGC	84628
rs113941483	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176117	ACTTTGGGAGGCCGA[G/T]GCAGGAGGATCACTT	84628
rs113975120	snp	G/T	0.0182019	0.0936463	intron-variant	NTNG2	GRCh38.p7	9:132183426	TGTTTTGTGTGTCCA[G/T]CCTGGCCCTTTGCTC	84628
rs114007101	snp	C/T	0.0345262	0.126772	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230410	CCCCGTCCCCACACC[C/T]TGCAGGTCATCATGA	84628
rs114026652	snp	A/G	0.0228947	0.104514	intron-variant	NTNG2	GRCh38.p7	9:132174588	AAGACGAGACCAGGC[A/G]TGTGATGACCTCAGC	84628
rs114075645	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132179088	AGGAGCTTCAGACCC[C/T]GGAGGCTCCACCCCA	84628
rs114147935	snp	C/T	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132210449	ATCTCCAGCTCTGTC[C/T]TCTGTCCCTTCATCA	84628
rs114167717	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132222482	TTCCAGTAAAACCTC[A/G]GCAGGGTTAGTGTCC	84628
rs114210579	snp	G/T	0.0162398	0.0886349	intron-variant	NTNG2	GRCh38.p7	9:132179812	GTCTCCAGGGCCTCC[G/T]TCACTGTCCTGTCCT	84628
rs114219553	snp	A/G	0.031825	0.122064	intron-variant	NTNG2	GRCh38.p7	9:132194799	GTCAGCCCTGCCACC[A/G]AGGAGCCCCAGGCAG	84628
rs114222674	snp	C/T	0.00159617	0.0282053	intron-variant, missense	NTNG2	GRCh38.p7	9:132237243	CCTCCCTGGGCTCTT[C/T]GAGGAGAGGGGCTGT	84628
rs114294878	snp	C/T	0.0193772	0.0965046	intron-variant	NTNG2	GRCh38.p7	9:132175553	CCGGGCCATGAGGAA[C/T]AGGAGAAACGGCAGA	84628
rs114352546	snp	A/G	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132180922	ACACACACACATATA[A/G]GGTTGCAAACACTTT	84628
rs114366000	snp	G/T	0.0158469	0.0875917	intron-variant	NTNG2	GRCh38.p7	9:132224430	AAGAATGGTTTCACC[G/T]CCCTAAAAATCCCTG	84628
rs114499111	snp	C/T	0.0168055	0.0901129	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132237357	GCTCGGAAGCCTTTG[C/T]TGGGCTCTTCCCTGG	84628
rs114605965	snp	C/T	0.0154538	0.0865337	intron-variant	NTNG2	GRCh38.p7	9:132221474	CAGAGAGACCAGAAG[C/T]ACCTGCATTGACCAG	84628
rs114607405	snp	C/G/T	0.0189856	0.0955633	intron-variant	NTNG2	GRCh38.p7	9:132182066	AGAGAAGGGAGGGCC[C/G/T]GGAGGAGTGACGGTG	84628
rs114607739	snp	A/G	0.0356815	0.128715	intron-variant	NTNG2	GRCh38.p7	9:132224016	CTCCCCTTCTGGCCC[A/G]GCAACTCTTGATCCT	84628
rs114625625	snp	C/T	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132176816	CCCACCAGCAATGTA[C/T]GAGAATGCCAGTTTC	84628
rs114669299	snp	A/T	0.0244538	0.107838	intron-variant	NTNG2	GRCh38.p7	9:132224020	CCTTCTGGCCCGGCA[A/T]CTCTTGATCCTCCTT	84628
rs114704298	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227247	AACACACGTGCGTGC[A/C]TGCACCCCCACACAC	84628
rs114715382	snp	C/T	0.00636936	0.0560724	intron-variant	NTNG2	GRCh38.p7	9:132171082	GCCGAGATTCCCAGA[C/T]GCGGGCCTTGCTTGC	84628
rs114806854	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132198815	TGTGATACATCGTTA[C/T]CTGGTTCCCTGGGGG	84628
rs114939116	snp	C/T	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132224080	GAAACTGTGGACTCC[C/T]GTGATGCCTTCTTCT	84628
rs114940454	snp	A/C	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132178262	TTCTCAGAGCAGGGT[A/C]CTTGGAAGGAGATGC	84628
rs114942249	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132193773	CATAACAAAGTAGCA[C/T]ACGAGACCCAGGTGG	84628
rs114948917	snp	C/T	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132173910	GATGAGATGGACGGA[C/T]GGACGGACAGATGGA	84628
rs115141786	snp	A/G	0.046775	0.145601	intron-variant	NTNG2	GRCh38.p7	9:132207461	GGCTGTCCGCTCCCT[A/G]AGCATCTGTCTTACA	84628
rs115145339	snp	A/G	0.0185938	0.0946107	intron-variant	NTNG2	GRCh38.p7	9:132201877	CCCACCCCCTGGAGC[A/G]CTCCCCGCGGGGGCA	84628
rs115149252	snp	A/G	0.0260105	0.111035	intron-variant	NTNG2	GRCh38.p7	9:132190320	GAAATTGGGGGACTC[A/G]CCCAAGCCTGTGGAG	84628
rs115273869	snp	C/T	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132201996	GCAGACAGCTAACAT[C/T]TAGACACAAGCATGT	84628
rs115331321	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132233311	CATGCATGCACACAC[A/G]CAGGCATGCACACGC	84628
rs115337700	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229111	AGTCCCCGGGAATTG[C/T]CTTTGAGGCCCCCAA	84628
rs115390325	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132204244	CGGCTCCTGCAGACC[C/T]AGCTTCCCCAGACCC	84628
rs115391634	snp	G/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132227661	ACGGCCTGCACCAGA[G/T]TCCCCCCGCACGTGC	84628
rs115542643	snp	C/T	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132226169	CCCCTCATCAACTTT[C/T]GGTTACCCCGAGGTA	84628
rs115552680	snp	A/G	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132235056	GTTAGTCTACGGGCT[A/G]AGCGTTGTGTCACTG	84628
rs115630838	snp	G/T	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132168255	GGCCGTCCCTGGCAG[G/T]GCAGGGCAGAGCTGG	84628
rs115836355	snp	A/C	0.0248432	0.108648	intron-variant	NTNG2	GRCh38.p7	9:132176048	ACATAACATAAAATT[A/C]ACCAGTTAAACAACG	84628
rs115873222	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132212750	CCCATGAATTAGCTA[C/G]AAGTGCAGTTTGCTA	84628
rs115905823	snp	C/T	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132179709	CCTCTCGTAACAGGA[C/T]GGAGCCAGGTCAGAG	84628
rs115936541	snp	G/T	0.0314385	0.121371	intron-variant	NTNG2	GRCh38.p7	9:132176304	TTAGTCCCAACACGT[G/T]TCCATCGCCCCAATA	84628
rs115973739	snp	A/G	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132214039	TGAAATCCCCGTGGG[A/G]CTTTGCCTTTGCAGA	84628
rs116083242	snp	C/T	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132199770	TAGCAGAAACCAGGC[C/T]GGAGTCAGATCTTTC	84628
rs116118336	snp	A/G	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132203472	ATGGAGACAGCAGGC[A/G]CCTCACAAGACAGTG	84628
rs116127222	snp	C/T	0.0154538	0.0865337	intron-variant	NTNG2	GRCh38.p7	9:132189237	GTGTGCCACCATGCC[C/T]GGCTAGTTTTCTTTT	84628
rs116128300	snp	C/G	0.00636936	0.0560724	intron-variant	NTNG2	GRCh38.p7	9:132182741	CCAACACTTGGGGCA[C/G]TCTTCTCGAAGGCCT	84628
rs116143831	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132196126	GTCCATAATTTACAT[A/G]AGAGTTCACTTACTG	84628
rs116290851	snp	C/T	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132192813	AGAAAATTGTGTTGG[C/T]CGCGGCTCGGGATTT	84628
rs116344804	snp	A/T	0.45762	0.139261	intron-variant	NTNG2	GRCh38.p7	9:132214876	AAATTCAAAAAAAAT[A/T]TTTTTTTTTTTTAGA	84628
rs116402485	snp	A/G	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132210477	TCAGTCAACAGTCAT[A/G]CAGGAATGAGAAGCT	84628
rs116438205	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132184339	GAGAGGGAAGGGGCC[A/G]AGGAGGGGGAGTCAC	84628
rs116438622	snp	C/T	0.0193772	0.0965046	intron-variant	NTNG2	GRCh38.p7	9:132223705	ACACCCCAGGCGGGA[C/T]GGGTGGGCCCAGGTG	84628
rs116457503	snp	C/G	0.00159617	0.0282053	intron-variant, missense, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237433	AAGCTGTGGGCACCC[C/G]TGCCGCTGCCCCTGC	84628
rs116492793	snp	A/G	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132181001	AATCATCTGGCCTGA[A/G]CAGGTTCTGCCTTCT	84628
rs116605146	snp	A/C	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132227257	CGTGCATGCACCCCC[A/C]CACACACACCTTGTT	84628
rs116818392	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220966	AGGTCTTATGAGTCT[A/G]ACATTAAAAAAAACA	84628
rs116829490	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132202464	GCAAGTCCCAGCCAC[A/G]CCCCCTCCCTGCCTC	84628
rs117054716	snp	C/T	0.0260105	0.111035	intron-variant	NTNG2	GRCh38.p7	9:132171776	ACACTCTGCCTCCTG[C/T]CAGACCTTGAGGATC	84628
rs117070574	snp	A/C	0.0174175	0.0916809	intron-variant	NTNG2	GRCh38.p7	9:132165084	TGGGAAATCAAATGC[A/C]ATCATCGAAGACATA	84628
rs117074616	snp	A/G	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132234387	CCAAAGGAGCAGACC[A/G]GGCTTCCATGGGGCC	84628
rs117104017	snp	C/G	0.0165278	0.0893908	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230967	ACCCACGCCACTTCT[C/G]TCACCTGGATCTGGG	84628
rs117140963	snp	G/T	0.0162398	0.0886349	intron-variant	NTNG2	GRCh38.p7	9:132189464	AATTTTGCAAGACCT[G/T]TGTGTCCAGGTCCCT	84628
rs117298742	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132224982	GGCTGGAGTGCAGTG[A/G]TGCAATGGCTCACTG	84628
rs117336340	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239478	ACCCTTGCGGTTCTC[C/T]GGTAAGTTTTGCACT	84628
rs117518797	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164910	GGGCAGCAAGTGTCC[A/G]CCACTTCGGTTTGTC	84628
rs117539449	snp	C/T	0.0622301	0.165053	intron-variant	NTNG2	GRCh38.p7	9:132202689	GGCCTCCGCCCCCAC[C/T]CTCCACACAACCATT	84628
rs117730917	snp	G/T	0.0123036	0.0774623	intron-variant	NTNG2	GRCh38.p7	9:132170899	CTCTGGAGCGCTGGG[G/T]TGGGGTTGGTCCAGG	84628
rs117829780	snp	C/T	0.0293609	0.117552	intron-variant	NTNG2	GRCh38.p7	9:132227075	ATAATCTTCCCTGCC[C/T]GTCAATCCCAGGAGC	84628
rs117895820	snp	A/C	0.0193772	0.0965046	intron-variant	NTNG2	GRCh38.p7	9:132238066	GGTCCTCTAGAGATA[A/C]ACAGATGGTGTTTCA	84628
rs117978557	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132167923	GCTCTGGCCCAGTGA[C/T]GTCTGTGGGCTTCTG	84628
rs118077717	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132189402	GTCATGGAGAAGTAC[A/G]ATTGGCTTAAAAAAA	84628
rs118155182	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228732	CCAGCTAATTTTCGT[A/G]TTTTTTTCAGAGAAA	84628
rs137862169	snp	G/T	1.67478e-05	0.00289372	missense	NTNG2	GRCh38.p7	9:132167039	CCTGAGAGGTTCTGC[G/T]CCCATGTAAGTCCAC	84628
rs137980796	snp	A/G	0.0162398	0.0886349	intron-variant	NTNG2	GRCh38.p7	9:132178060	TCTCCTGTTGTGCCC[A/G]TTTTATAGATGAGGA	84628
rs137987426	snp	G/T	0.0138799	0.0821421	intron-variant	NTNG2	GRCh38.p7	9:132219082	TCTGGCCGGGTGTGG[G/T]GGCACACGCCTGTAA	84628
rs138021392	snp	C/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132175610	TTGGTTTGCAGGATC[C/T]GATTTGTTTTTCATC	84628
rs138072540	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132174417	ATGCTGCGGATGAGA[A/G]CTTGGGCTTCTGGAG	84628
rs138095120	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202569	GGGGAAACTCAGGTG[C/T]GGAGCCTGGAGAGTG	84628
rs138164196	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132192740	GTGGAATTCTGAGAC[C/T]TTGGGGAGCAAAATC	84628
rs138248774	in-del	-/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239641	TGGGGCTGGTGTGTG[-/T]GGGGGGTCCCCCTCC	84628
rs138346607	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225237	GTTTTGTCTTGTTTT[G/T]TTTTTGTTTTTGTTT	84628
rs138360074	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233324	ACACAGGCATGCACA[C/T]GCACATGTACACACA	84628
rs138376074	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177324	AATGTGTGTATTTTT[C/T]TCTTTTGTTGCTTGT	84628
rs138396464	snp	A/G	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228730	GCCCAGCTAATTTTC[A/G]TGTTTTTTTCAGAGA	84628
rs138426229	in-del	-/CA	0.194278	0.243711	intron-variant	NTNG2	GRCh38.p7	9:132210900	ATGTACCCGCCAAGT[-/CA]CACACACACACGCAG	84628
rs138439530	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132187362	CAGCCCTAAAATGCC[A/T]GGTTGGTTTACGCTG	84628
rs138460326	snp	C/T	0.000109073	0.00738408	intron-variant	NTNG2	GRCh38.p7	9:132226833	TGACATCTCTGCCCT[C/T]TCGGTGTCTCCCCAG	84628
rs138471979	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181567	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGTC	84628
rs138482884	snp	C/T	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132223314	CCTTGCTCTGGAAGG[C/T]GGCCCCCAGGGGACC	84628
rs138493692	snp	A/G	1.64866e-05	0.00287106	missense	NTNG2	GRCh38.p7	9:132166916	TCCTGGGTGACCACA[A/G]ATGAGGGCCCCACCT	84628
rs138616053	snp	A/G	1.70647e-05	0.00292097	synonymous-codon	NTNG2	GRCh38.p7	9:132198556	CACCTATGTGCAGCG[A/G]GAGAACCTCTACAAG	84628
rs138637816	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132238569	GGTCTGGCAGGTGGG[C/T]GTTTTCCTCCCAGCC	84628
rs138703012	snp	A/G	0.0138799	0.0821421	intron-variant	NTNG2	GRCh38.p7	9:132172753	TTTTTTTTTGGAGTC[A/G]AAGTCTCGCTCTGTC	84628
rs138727136	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132211057	ACCCCTGCTCACAGA[C/T]GCGGACCCACAGGGT	84628
rs138731958	in-del	-/AGAC	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230169	CACACTGCACTTCTT[-/AGAC]AGGAACACTCCATAC	84628
rs138741203	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132210471	CCTTCATCAGTCAAC[A/T]GTCATGCAGGAATGA	84628
rs138742165	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132169714	GTGTCACGGTGCTGG[C/T]GGGACGGCACAGCCC	84628
rs138750190	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227919	TGCCACTTTACGGCC[A/G]TTCTCAAGTGTGTGG	84628
rs138763531	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132206405	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAACA	84628
rs139001117	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191153	GTGCCCAACCCAGCC[C/T]GGGCACAGGGCTGGC	84628
rs139134492	snp	C/T	0.000107406	0.00732743	intron-variant	NTNG2	GRCh38.p7	9:132238944	TCTCTCTTCCTGAAT[C/T]CGATGGAAGGGTGGG	84628
rs139145121	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132171069	GATGGAGCTGGGAGC[A/C]GAGATTCCCAGATGC	84628
rs139147768	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193529	GCCTGGGAAATGGCA[C/T]AGCTTCAGTGCTGGG	84628
rs139178536	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132235122	CCAGGGGTCAGGAAG[A/G]TAGAAGGGCAGTGAT	84628
rs139186629	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132165762	TCTGACCCCCAAGCC[C/G]GGGCACTTCTGCTGA	84628
rs139239505	snp	C/T	0.000897626	0.0211662	synonymous-codon	NTNG2	GRCh38.p7	9:132226912	CCTGCAGTGCGAGTG[C/T]GAGCACAACACCACC	84628
rs139280811	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132214417	ATCCTTCATGTGGCT[-/G]GTCAGGCCCCCAGCT	84628
rs139309074	in-del	-/GGAC			intron-variant	NTNG2	GRCh38.p7	9:132174214	ATTAGACGGACAGAT[-/GGAC]GGACGGACAGACAGG	84628
rs139378477	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201015	GCCCTGCAGGCTCCT[A/G]GCTTGTCTTCTGACC	84628
rs139381316	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225238	TTTTGTCTTGTTTTG[G/T]TTTTGTTTTTGTTTT	84628
rs139398067	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240211	GGTCTGAATTCTGGC[A/G]GCAGCCTTCAGATAA	84628
rs139441520	snp	G/T	0.00478085	0.0486577	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231200	AGAGTTCCCCAGGAG[G/T]GCGAGGGCGACATGG	84628
rs139558522	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132221039	TACAGTCCATGCGCC[C/T]ATCTCCCCCAGTCAT	84628
rs139560389	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132176426	CTAGACATTTCATAC[A/G]AATGGAATCAGACAA	84628
rs139599290	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132217804	CAACTTTCCTGAGGT[C/T]ACACAGTCGTTGGCA	84628
rs139746624	snp	C/G	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132185239	ACCCCCTTCCCCACC[C/G]TGGGCCTCTGTTGGA	84628
rs139748501	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229313	CTCAGTAAGTGGCAC[C/T]GACACCCACGGGGCC	84628
rs139761613	snp	C/T	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132179429	CCCATCTGCCAGCTG[C/T]GGTCTTCTCTGTGGT	84628
rs139789314	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132225122	GGGTTTCACCATGTC[A/G]GACAGGCTGGTCTTG	84628
rs139802344	snp	C/T	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132221576	CAGGGCAATTCTCTC[C/T]TTTGGAAGAGGAGGC	84628
rs139836050	snp	A/G	0.0111196	0.0737302	intron-variant	NTNG2	GRCh38.p7	9:132202913	ACCTGTTGGAACCTC[A/G]GTTTTCTCATCTGCA	84628
rs139838218	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132235758	TGGGCCTGAGACCCC[A/G]GGGAAGCGCCCTCTT	84628
rs139857272	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132200519	CCGGGAAAAACATCA[C/T]GGGTTGGGGAGAAAG	84628
rs139932744	snp	C/G	0.000153988	0.00877328	missense	NTNG2	GRCh38.p7	9:132198382	CAAGAAGGAGAAGCA[C/G]GTGCGCTTCGAGGTG	84628
rs139948966	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176334	AGAAAACCCTGCACC[C/T]GTTAGTTACTCCCCA	84628
rs140049160	snp	A/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132182792	GACCCCACCAGGAGC[A/G]GAGCGGGCAGGGACC	84628
rs140070239	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179984	TGTGTGGATCCCTGT[G/T]AATCTAACCCTGGAG	84628
rs140142808	in-del	-/G	0.200182	0.244986	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239640	CTGGGGCTGGTGTGT[-/G]GGGGGGGTCCCCCTC	84628
rs140174486	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171803	GATCATGAAATGTTT[C/G]CATCCAACAATGCAG	84628
rs140215157	snp	C/T	0.0126979	0.078662	intron-variant	NTNG2	GRCh38.p7	9:132187157	ATGCCCACTGTGGCC[C/T]CCCTGGGGGAGGAGC	84628
rs140393152	snp	C/G	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132213509	GGCAGCATCATTCCT[C/G]ACTGCAGTCCAGGTC	84628
rs140396907	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243964	TCACATTCTTCCTTA[C/T]GCACAGAACCCCACT	84628
rs140419835	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132232862	CATCAGCTCCTGCCT[C/T]GGCCTGTTGCTGGGT	84628
rs140463143	in-del	-/GGT	0.0119091	0.0762411	cds-indel	NTNG2	GRCh38.p7	9:132242687	AGGAGAGAAGGAAGG[-/GGT]GGGGGGCCTGGAAAC	84628
rs140585876	snp	A/C	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132221870	GGCCGGTCTTCTATG[A/C]ATCTTTACTAAGCCA	84628
rs140618958	snp	A/C	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132191662	CTGCAAGCTCCACCT[A/C]CTGGGTTCACGCCAT	84628
rs140639545	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132226354	GTTGCCCTCAAGGGC[A/G]TGGCTGTGGGCCACA	84628
rs140712497	snp	A/G	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132223007	TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGAGGG	84628
rs140767956	in-del	-/TTGTC	0.484701	0.0861117	intron-variant	NTNG2	GRCh38.p7	9:132225225	GCTGGCCCTTTTGTT[-/TTGTC]TTGTTTTGTTTTTGT	84628
rs140784706	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132222694	GTGCCCCCTCTCCCA[C/T]GGCCCACCCAGGACC	84628
rs140839116	in-del	-/AC	0.417503	0.197836	intron-variant	NTNG2	GRCh38.p7	9:132233332	TGCACACGCACATGT[-/AC]ACACACACACACACA	84628
rs140872009	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177066	GTGATCTTGGCTCAC[C/T]GCAACCTTCACCTCC	84628
rs140892939	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218566	CAATGGCATGACCTC[A/G]GCCTACTGCAACCTC	84628
rs140962531	snp	A/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132207156	TCTGCGAGCTTTCTC[A/G]CCATCATATTAATTC	84628
rs140963531	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132209537	AAGCCACGCGGGAGC[A/G]GTTCCTGCAGGGCAG	84628
rs141003041	snp	A/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132204907	ATAGTGAGACCCCCA[A/T]CTCAATGAAAACAAA	84628
rs141066789	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132166171	CCAAATAGCCTTCTC[C/T]CCAGTGAACACCTCA	84628
rs141080327	snp	G/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132177652	AATCTCTGGGTTTTT[G/T]TGTTTGTTTGTTTGT	84628
rs141080342	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222507	GTGTCCAGGCTCTCA[A/G]GGGAAGATGGAGTTA	84628
rs141133491	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132234862	CAGCTGGAAAGTCTT[C/T]CGCACTTGTTAGCTG	84628
rs141223633	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132218989	GCGTACAATTCAGTC[A/G]CTTTTAGGTTATTCA	84628
rs141232015	snp	C/T	0.0126979	0.078662	intron-variant	NTNG2	GRCh38.p7	9:132202059	TCCCTAGCCCTGGCC[C/T]GGTGGCTGCCTCATT	84628
rs141309731	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132176886	TTTGTCTTATTAGGA[C/T]GAGCCTAGTGGGTGT	84628
rs141328269	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191003	GATTCCTCAAGGTTG[C/G]GTCCCGTGGAGTCCA	84628
rs141458414	snp	G/T	0.0138799	0.0821421	intron-variant	NTNG2	GRCh38.p7	9:132181006	TCTGGCCTGAGCAGG[G/T]TCTGCCTTCTGGGGG	84628
rs141462972	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183482	AGACTAGTCGAGTGT[C/T]CCTCCACCTGTCCTG	84628
rs141465317	snp	C/T	0.00405473	0.0448433	intron-variant	NTNG2	GRCh38.p7	9:132227037	GTACGTGCCATGCCC[C/T]GGGGCCACGAGCCCA	84628
rs141482864	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132223902	CCTCCGTCTCCTGGT[C/G]TGGCCTCCTCCACCC	84628
rs141502350	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132205102	AGATTTAGCAATTCC[A/G]CTCCTAGGTATAGAC	84628
rs141571841	snp	C/T	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132178879	AAGAATTTCTTGAAC[C/T]TGGGAGGCGGAGGCA	84628
rs141605288	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173739	AGGAGCACCATGCTG[C/T]GGATGAGATGGATGG	84628
rs141624215	snp	C/T	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132203187	TGGAAACACAACTTA[C/T]GTGGAAGCCAGGCAT	84628
rs141643985	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201716	ATCGAGCATTTGCTA[C/T]GGGCTCATTTGCTAT	84628
rs141677568	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211014	GCACCCAGTCATAGA[C/T]ACATCACACTCCACA	84628
rs141720966	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132238313	TCTGGTCCTTGGAGC[A/G]GAGCTGGTTAGGCAG	84628
rs141875771	in-del	-/TGTGTGTGTGTGTATGTG			intron-variant	NTNG2	GRCh38.p7	9:132216415	CTCTCTCTCTCTCTC[-/TGTGTGTGTGTGTATGTG]TGTGTGTGTGTGTGT	84628
rs141908420	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132188990	GGCTGAGGGCCCATC[A/G]TAACAGACAGATTAA	84628
rs141926797	snp	A/G	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132217522	TTGCCTCATTTCCTT[A/G]TCTGTGAAATAGAGA	84628
rs142004044	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132216787	ATCTGGGCTGGAGTG[A/C]AGCAGGAGCCCAGAC	84628
rs142038376	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181470	GGATTACAGGCACCT[G/T]CCACCATGCCTGGCT	84628
rs142075133	in-del	-/T	0.0119091	0.0762411	intron-variant	NTNG2	GRCh38.p7	9:132226458	GTCTACACCAGGTGC[-/T]TGGCAGCAGCCTCTG	84628
rs142135792	snp	A/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132225916	GCATCCCCTGGTGTC[A/G]TTCAGGGTGATGCTC	84628
rs142171436	snp	A/G	0.0158469	0.0875917	intron-variant	NTNG2	GRCh38.p7	9:132180807	GAGCGGGAGCTTCTC[A/G]CTTTTAATGGTCATG	84628
rs142235796	snp	A/G	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132193951	CACATGGGCCCCAGC[A/G]TCTCATCCGGCAGCC	84628
rs142276229	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132212479	AATTTGATTTAGCCA[A/G]TGAACTCAATTGCCG	84628
rs142277729	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132220591	CCCAAGTAGTTGGGA[A/T]TACAGGCACCCACCA	84628
rs142318147	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240474	GAGCAGGAATAGGCT[G/T]TTCCTCCACTCCCCT	84628
rs142318307	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132197337	GAGGTTGCTGTGAGC[C/T]GAGATCGCCCCACTG	84628
rs142321324	snp	A/G	0.0209421	0.100162	intron-variant	NTNG2	GRCh38.p7	9:132200262	GGCAGTCCGGGCCAG[A/G]AGCCTGGCTTAGGCA	84628
rs142385233	snp	A/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239732	GGGGGCCAAAAGATC[A/G/T]CCTTGCTGCGTGCAT	84628
rs142389154	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132171662	TCCTCCCCCAGGGGG[C/T]CTGCTGGGCTGTTGA	84628
rs142424514	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132237337	CCTAGAGCTGGCCCA[C/G]GGCGGCTCGGAAGCC	84628
rs142471343	snp	C/G/T	3.31434e-05	0.00407073	synonymous-codon	NTNG2	GRCh38.p7	9:132198124	GGAAGCCAACATCAC[C/G/T]CTTTCGTGGAACAAG	84628
rs142515065	snp	C/T	0.000181355	0.00952075	synonymous-codon	NTNG2	GRCh38.p7	9:132166942	CACCTGGGAGTTCTA[C/T]GCCTGCCAGCCCAAG	84628
rs142580225	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165881	ATAACCCAGTTTTCT[C/T]GGGAGACTTTGCTAA	84628
rs142599711	in-del	-/GACA	0.441705	0.160466	intron-variant	NTNG2	GRCh38.p7	9:132174326	ACGGACGGACGGACG[-/GACA]GACAGACAGACAGGT	84628
rs142619742	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132218523	TTTTTTGAGACCAAG[A/T]GTTGCTCTTGTCCCC	84628
rs142653026	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132201327	AGCCTCTGCGGGCGG[C/T]GGGGAGGAGCCGAGG	84628
rs142697386	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202683	GGGAGGGGCCTCCGC[C/T]CCCACCCTCCACACA	84628
rs142738574	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132223430	GAGGGAGGCCGGATG[C/T]GAGGAGGGAGCTCTG	84628
rs142738640	in-del	-/A	0.398714	0.200958	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243061	TAGGAGCCTCCCCAC[-/A]CTGAAAGGCTGCCTC	84628
rs142749895	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175353	GCTCTGAAGGAGCAA[A/G]AGGGGCAGGAGGGCA	84628
rs142759629	snp	C/T	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132207994	CTGTGGTCTCAGATA[C/T]CTGGGAGGCTGAGGT	84628
rs142769306	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132216033	CTTCCTAGGGTTACA[A/G]GACACCGACTGATTC	84628
rs142774035	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221342	AGAGACAGGAGAAGA[C/T]GGAGACATGGAGAGA	84628
rs142790275	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229119	GGAATTGCCTTTGAG[A/G]CCCCCAAGCCCCAGG	84628
rs142906524	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203485	GCGCCTCACAAGACA[A/G]TGGACCAAACATTCC	84628
rs143019623	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132175178	AGACAGTCCACTCCC[C/T]CTGCCCACCTCATCC	84628
rs143030058	snp	A/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132186386	AAGCAGAATGTGTCC[A/T]TTAAGAAAACAATAA	84628
rs143058075	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187650	AGAGAGTTAGAGACC[A/G]TCAGGGCCGCTAGAA	84628
rs143097071	snp	C/T	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132182361	GGGCTCCAGGCCTGT[C/T]TGCTTGGCACGGGGC	84628
rs143121890	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243158	CTCAGGGAGAATCCT[A/C]GCAGAGGTTGAATCC	84628
rs143149907	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197582	GGAGGACAGCTGTCC[C/T]GGGGAGGCCCAGGCA	84628
rs143156220	in-del	-/C	0.00953873	0.0683987	intron-variant	NTNG2	GRCh38.p7	9:132171165	GAGGCAGCACTACCT[-/C]CTGACAAGAGCTACA	84628
rs143182091	snp	A/G	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132211333	GAGGTGCAGGCTGGC[A/G]TCAGGATTTGGTTTC	84628
rs143295457	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132200843	AAACCACCCCATATA[C/T]AGGCACTGTTGTGGA	84628
rs143352696	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132219930	AGACCACTTTCCAAA[A/G]CAGCTGCACAATTTT	84628
rs143413424	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232715	TCCCCCGCCACCCTG[A/C]AGGGAGGACCTGGTG	84628
rs143435643	snp	A/G	0.0103295	0.0711199	intron-variant	NTNG2	GRCh38.p7	9:132210637	GGCTCCTGTCCCCCC[A/G]ACCCCAGCTCTGTGG	84628
rs143517497	in-del	-/AC	0.207559	0.246371	intron-variant	NTNG2	GRCh38.p7	9:132187541	GAAGGAGAATGAGAA[-/AC]ACACACACACAGAGA	84628
rs143527538	in-del	-/GA			intron-variant	NTNG2	GRCh38.p7	9:132170711	AGCTGACGAGCAGGT[-/GA]GAGAGAGAGAGAGAA	84628
rs143538035	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132178152	CTAGGCCACAGTGAG[A/G]CCTGAGGAGGGGAAA	84628
rs143571270	in-del	-/CTC			cds-indel	NTNG2	GRCh38.p7	9:132242387	TGTCTTTCTCTCTCT[-/CTC]TTTTTTTTTTTTTTT	84628
rs143732255	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201794	TAGCCGTTTAATTCC[C/T]CAATGGTTATTGAAT	84628
rs143736959	in-del	-/GAGCAAGACTCT	0.469049	0.120489	intron-variant	NTNG2	GRCh38.p7	9:132174905	CCAGCCTGGGCGACA[-/GAGCAAGACTCT]GTCTCAAAAAAAAAA	84628
rs143764418	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195848	TGTTGCCTAGGCTGA[A/T]CTTGAACTCCTGGCC	84628
rs143777458	snp	A/C	0.00636936	0.0560724	intron-variant	NTNG2	GRCh38.p7	9:132181849	TAGAGGAGGCTGGCA[A/C]CTCCAGCCTGGGCCG	84628
rs143842884	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132196877	TCTGTCCAATTGGCT[A/G]TAAATTGGGGGTTCC	84628
rs143921690	snp	A/T	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132171585	ACACATCTTACTCAG[A/T]TAGAACCTGCTTTAG	84628
rs143941243	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175907	CAGATTGGTCAGAGA[C/T]AAAACCACACAAAAC	84628
rs143993617	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132195058	CACAAGTGGTCCGGA[A/G]CACTGGGTGGTTGTT	84628
rs144069634	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190592	GGCACATTTACCTCC[A/G]TTCTTGCTAACAGTT	84628
rs144070298	snp	A/G	0.0252325	0.109451	intron-variant, missense	NTNG2	GRCh38.p7	9:132235711	CCCAGGTGGCCTCCC[A/G]TGCAGAAGGTATGGG	84628
rs144185250	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132163775	GCCAGCTCGGGAGGC[A/G]CTAATTCAATAAGAC	84628
rs144209257	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132176717	CTACCTAAAAGTGGA[A/G]TTTCTGGGTCACAAG	84628
rs144232110	snp	C/T	0.0252325	0.109451	intron-variant	NTNG2	GRCh38.p7	9:132212331	AAGCCTCCCAGCACC[C/T]GCCCGTCAGCCTCTG	84628
rs144243221	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132223706	CACCCCAGGCGGGAC[A/G]GGTGGGCCCAGGTGC	84628
rs144328611	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132178414	AGGTACTTAATAAAT[A/G]CTGAAGATAATTATC	84628
rs144337794	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132206855	TCCACTGAGAAGTGC[C/T]GGTGTTGGGAAGGGG	84628
rs144345408	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132218015	AGTGTCACTGGTGTG[C/T]GTGGCAGCCTGTGGC	84628
rs144347493	snp	A/G	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132174260	TGCTGTGGATGAGAT[A/G]GATGGATGGACAGAC	84628
rs144387506	snp	C/G	0.000798403	0.0199641	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231426	GGGTGCACCGTCACC[C/G]TCCACCAGGGCTCTG	84628
rs144417503	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132224826	TGTGTACCTCTCACC[C/T]GACTGCAGTTACCAA	84628
rs144472764	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132203330	GGGTGACAGAGAGAG[A/G]TCCTGTCTCTAAAAA	84628
rs144579919	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199076	GGACTGCCTAGGATG[A/G]CTGGGGCTGCACAGA	84628
rs144651817	snp	C/G	0.000491705	0.015672	synonymous-codon	NTNG2	GRCh38.p7	9:132198496	CAAGGAGTTCTTCAC[C/G]CTCACCGACCTGCGC	84628
rs144678158	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176408	TCCATGAATTTAGCT[A/T]TGCTAGACATTTCAT	84628
rs144709380	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132228059	CCCAGCGAACCTCGG[A/G]GCCCTCCCAGGTTTC	84628
rs144738721	snp	G/T	0.0107246	0.0724382	intron-variant	NTNG2	GRCh38.p7	9:132172492	CTTGGCACATAGTAG[G/T]TGCTCACTGCGTGCT	84628
rs144777882	snp	A/G	0.0325976	0.123435	intron-variant	NTNG2	GRCh38.p7	9:132209894	TGGGAAGAATCCACC[A/G]GGACTGAAGATAGCT	84628
rs144921624	snp	A/G	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132205758	TGGGAGCGGGTGCCT[A/G]TAATCCCACCTACTT	84628
rs144972533	snp	A/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132205048	AACGGTGCAGCCACA[A/G]GGGAGAACAGTATGG	84628
rs144998574	snp	C/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132180476	CACCCAGGCAACATC[C/G]AAAACCTTTGCCCAC	84628
rs145024500	snp	A/G	0.0126979	0.078662	intron-variant	NTNG2	GRCh38.p7	9:132221695	GCTGGCCAGGATGGA[A/G]CCTGGGCAGAGCCAG	84628
rs145031494	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222609	AGAGAATTCCAGAGA[C/T]GTCCTTCGTCCTGGG	84628
rs145109920	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191070	GTGTCTTATCTGAGA[C/T]GTGGAGCTGACTGTA	84628
rs145138227	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228742	TTCGTGTTTTTTTCA[A/G]AGAAAAGGTTTTGCC	84628
rs145183618	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132187882	AACTTGAGACTTTAG[A/G]ATGTCAGGGTCAGAG	84628
rs145232247	snp	A/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132205255	ATGTGACCCATCCAT[A/G/T]TAATGGAATATGATT	84628
rs145311058	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132185450	ACTTTTTTCCTCCCT[C/T]CGTGATAAAATATTC	84628
rs145393336	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132201176	CAGGGCCTGGTGGTG[C/T]CCCTTCAACCCCAGC	84628
rs145479097	snp	A/C	0.000153988	0.00877328	synonymous-codon	NTNG2	GRCh38.p7	9:132226933	CAACACCACCGGCCC[A/C]GACTGCGGCAAGTGC	84628
rs145627206	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179083	CCATGAGGAGCTTCA[A/G]ACCCTGGAGGCTCCA	84628
rs145691736	snp	C/G	0.0107246	0.0724382	intron-variant	NTNG2	GRCh38.p7	9:132171853	TCTGGCCTCCTTCCC[C/G]CTCTGTGTTTCTGGC	84628
rs145710375	snp	A/G	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240223	GGCGGCAGCCTTCAG[A/G]TAATTCCATCAACTC	84628
rs145749208	snp	C/T	0.0166325	0.0896639	intron-variant	NTNG2	GRCh38.p7	9:132218685	TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT	84628
rs145788429	snp	A/G	0.00124824	0.0249512	synonymous-codon	NTNG2	GRCh38.p7	9:132239240	CTACCGCAACGGCTC[A/G]GCAGAGCTGGATGAT	84628
rs145792244	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132215550	GAACCACTGCACTCC[A/G]GTCTAGATGACAAAG	84628
rs145822712	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226501	CCACATCAGTCAAAG[G/T]CTAGGGTGATCAGAA	84628

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