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
rs145831164	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196273	TCGGCTCACTGCAAC[C/G]TACGCCTCCAGGGTT	84628
rs145850105	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236291	AATGTGTGGGTTAAA[A/G]GAGGGAGGGCGGGGT	84628
rs145858749	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132223107	TGACAGAGTGAGACT[C/T]GGTCTCAAAAAGCAA	84628
rs145900539	in-del	-/GA			intron-variant	NTNG2	GRCh38.p7	9:132180688	TGCTTCAGGGAGACG[-/GA]GAGAGAGAGAAAGAG	84628
rs145922547	snp	A/G	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132197671	TGTATTCCAGGCAAC[A/G]GGGAGCCATGGAGGG	84628
rs145932301	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132202840	TGTGTCTTTGCAAAG[C/T]TCCTCAAGTGAGCTG	84628
rs145944298	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132200313	CTGGGGAGCCCAGCT[A/G]GGATGATCACTGTGG	84628
rs145954602	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239493	CGGTAAGTTTTGCAC[A/T]GGAGTTGCAAAACTT	84628
rs145960048	snp	C/G	8.66183e-05	0.0065804	missense	NTNG2	GRCh38.p7	9:132198299	TCCGCCCGCCGGGCC[C/G]GCGACATGTCATCCT	84628
rs146054051	snp	C/T	0.0185938	0.0946107	intron-variant	NTNG2	GRCh38.p7	9:132182400	CCTCCTGCCCAGTTC[C/T]CCTCCCCTGCACTGG	84628
rs146064838	snp	A/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132179935	ACCTCTTGGGGTCTC[A/G]TTGGCAGGAGGGAAT	84628
rs146177146	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132170784	CCCACTCAGAGCAAT[C/T]GCCTCAGTGCAGCAG	84628
rs146182441	snp	A/C	0.000221631	0.0105246	intron-variant	NTNG2	GRCh38.p7	9:132238938	GAGGCCTCTCTCTTC[A/C]TGAATCCGATGGAAG	84628
rs146188409	snp	C/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132165396	ATTTATAGACCTACC[C/G]TCTAAGAATGATTTG	84628
rs146193581	snp	A/C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132235028	CCTGCCTGCCTTGCT[A/C/G]GCTGTGTGTCCCGTT	84628
rs146313535	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217697	AGAGCTTTATAGACC[A/G]TCTCCCACTTGATCC	84628
rs146343630	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132201609	TCTGGGATTTTACAC[C/T]GATCCTGTTCTGGGG	84628
rs146416955	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132197471	TAGAGAGTCGAGAAT[A/G]TGAATGGGAATTTTT	84628
rs146471804	snp	G/T	0.0123036	0.0774623	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237643	AACCCTCCTGGAGTA[G/T]CTGGGTCAAGGTTAA	84628
rs146564191	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132176817	CCACCAGCAATGTAC[A/G]AGAATGCCAGTTTCT	84628
rs146603714	snp	A/C	0.0252325	0.109451	intron-variant, missense	NTNG2	GRCh38.p7	9:132235714	AGGTGGCCTCCCGTG[A/C]AGAAGGTATGGGGGG	84628
rs146604599	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190804	GGAGCTCAGGCTTGG[C/T]ATCTGTGTAGGAGGC	84628
rs146697985	snp	A/G	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132226079	GTTCTGGGCTGGTGC[A/G]GCTCAGTGCCTGGAG	84628
rs146735380	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213307	AGCCTCCAGCCTGGG[C/T]GATGACAGAGTAAGA	84628
rs146757880	snp	A/G	1.65449e-05	0.00287614	synonymous-codon	NTNG2	GRCh38.p7	9:132239159	TGACTTCCTGAATGT[A/G]GTGACCTGCGTCAGC	84628
rs146802508	snp	A/G	0.0154538	0.0865337	intron-variant	NTNG2	GRCh38.p7	9:132213140	CATAGTAAAACCCTC[A/G]TCTCTACTAAAAATA	84628
rs146864007	in-del	-/T	0.0107246	0.0724382	intron-variant	NTNG2	GRCh38.p7	9:132186406	GAAAACAATAATACA[-/T]TTTTAAGTTCCTGGA	84628
rs146967239	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132219049	CTTTAGAACATTTCC[A/G]TCACCCTAAAAAGAC	84628
rs147027342	snp	C/T	0.00046168	0.0151864	synonymous-codon	NTNG2	GRCh38.p7	9:132166978	GCGCCTGAAGGACTA[C/T]GTCAAGGTGAAGGTG	84628
rs147053586	snp	C/G	1.64868e-05	0.00287109	synonymous-codon	NTNG2	GRCh38.p7	9:132166909	CTGCAAATCCTGGGT[C/G]ACCACAGATGAGGGC	84628
rs147081993	snp	G/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132216244	CCCTTGCTTCTTTCT[G/T]CAAACATTGAGCACC	84628
rs147109227	in-del	-/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132233559	GCACCCTCAGCCCTG[-/T]TATCAAGAAGCAGGA	84628
rs147155883	snp	C/T	0.0107246	0.0724382	intron-variant	NTNG2	GRCh38.p7	9:132211023	CATAGACACATCACA[C/T]TCCACATGGCTGCCT	84628
rs147197552	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132193742	CATGAGGCTTGTCTT[A/G]GTCAGCTCCGGCCAC	84628
rs147282769	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132193359	CCAATAAGCACATTA[A/G]CAACTCTATGATGGA	84628
rs147389138	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132175434	GGCTGGTCCAGAGCT[C/T]ACCAGGCTGGACCAC	84628
rs147418838	snp	C/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132225050	TCAGCCTCCCCAGTA[C/G]CTGGGATTACAGGTG	84628
rs147513994	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132211349	TCAGGATTTGGTTTC[A/G]GGACATGACTGGCCT	84628
rs147524457	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132207737	GCATGGAGGGGCTGA[C/T]GCTCCCGTAGTGGGA	84628
rs147561017	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185649	GCCTTTCCCCCGCCC[A/G]CCCCCTTATCTTTCT	84628
rs147571018	snp	A/C	0.0111196	0.0737302	intron-variant	NTNG2	GRCh38.p7	9:132181168	GGCTCACTGCAGCCT[A/C]GACCTCCTGGGCTCC	84628
rs147666298	snp	A/G	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132171887	AGCCTCCCTCCTCTC[A/G]CCGTCACAACCCTCC	84628
rs147674547	snp	C/G	0.0182019	0.0936463	intron-variant	NTNG2	GRCh38.p7	9:132236612	GTTTAGAGAGGGTCT[C/G]AGGCTCGGTTCCTAG	84628
rs147676192	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167437	ACTGTAAGCTCCCTC[C/T]GTTCATCCTTTCTGT	84628
rs147689661	snp	A/G	0.000383088	0.0138346	missense	NTNG2	GRCh38.p7	9:132226940	ACCGGCCCCGACTGC[A/G]GCAAGTGCAAGAAGA	84628
rs147747987	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240449	AGGCAACCAACTGGG[C/T]CCACCCCGGGAGCAG	84628
rs147778375	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132218986	AAAGCGTACAATTCA[G/T]TCGCTTTTAGGTTAT	84628
rs147874406	snp	C/T	0.0119091	0.0762411	intron-variant	NTNG2	GRCh38.p7	9:132205101	TAGATTTAGCAATTC[C/T]GCTCCTAGGTATAGA	84628
rs147885018	snp	C/T	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132201707	CAAACGTTTATCGAG[C/T]ATTTGCTACGGGCTC	84628
rs147926242	in-del	-/GGGGGGGG			intron-variant	NTNG2	GRCh38.p7	9:132208295	CAGTGTGATGTGGCT[-/GGGGGGGG]GTGGTGGGTGAGTAA	84628
rs147934555	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132171773	CAGACACTCTGCCTC[C/T]TGCCAGACCTTGAGG	84628
rs147944672	snp	A/G/T	0.00164035	0.028592	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166809	GGGCTTCTCTGGGCC[A/G/T]CGCCTCTGCAGACTG	84628
rs147994360	snp	A/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132210894	CCCTTAGATGTACCC[A/G]CCAAGTCACACACAC	84628
rs148031459	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132167963	CTGCAAAATGGGCAC[A/G]CTAAGAGCACACACT	84628
rs148063496	snp	A/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132173696	TGCTGCGGATGAGAC[A/G]GATGGATGGACAGAC	84628
rs148084014	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196975	TACATTTACCTGTTT[A/G]TCAAGTTCAGGAACA	84628
rs148116300	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132201930	TCAGATGAAGAAGCC[A/G]AGGACTCTGAGGTCA	84628
rs148151965	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132216245	CCTTGCTTCTTTCTG[C/T]AAACATTGAGCACCT	84628
rs148200962	snp	A/G	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132175228	ACTGTGCATCTGACC[A/G]GTGAATATTCTGAGA	84628
rs148259492	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243695	GCGAGGTTTAGACCT[C/G]GGTCCTTCCCTTGAG	84628
rs148321316	snp	A/G	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132223783	CCTGCCCAGGCTTTT[A/G]TCTCCCAGACAAACC	84628
rs148325549	in-del	-/A	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132205125	GTATAGACCCAACAG[-/A]ACTGAAAGAAGGGAC	84628
rs148325876	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237848	AGAATCTGGGACACA[C/T]GGGTCACCGATGCTG	84628
rs148357601	snp	C/T	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132178715	GGAGGCTGAGGCGGG[C/T]GGATTGTCTGAGCTC	84628
rs148367482	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132220561	GGTTCAAGTGATTCT[C/T]ATGCCTCAGGACCTC	84628
rs148374128	snp	A/G	3.29804e-05	0.00406068	synonymous-codon	NTNG2	GRCh38.p7	9:132166972	GGTGATGCGCCTGAA[A/G]GACTACGTCAAGGTG	84628
rs148445553	snp	C/T	0.00953873	0.0683987	intron-variant	NTNG2	GRCh38.p7	9:132218463	ACTTCCTTTGAGGCA[C/T]AATGTGATAGCGTTT	84628
rs148482237	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132200205	GAGTGAGAGGGCTGG[C/G]GCGGGCTGAGGGAGG	84628
rs148639221	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171624	TGCCTCAGTTTACCC[A/G]GCTGCAGAGCAAATG	84628
rs148643193	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239599	CAGGTGGCAGGCACT[C/T]AGTGGCAGAGGCCAC	84628
rs148674672	snp	A/G	0.0103295	0.0711199	intron-variant	NTNG2	GRCh38.p7	9:132180577	GAACTGGGTGGCCCC[A/G]GGCAAGTCTCTTCCC	84628
rs148687288	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193824	TTCCTTGTTCTGGAG[A/G]CTGAAAGTCCAAGAT	84628
rs148726526	in-del	-/C/CC			intron-variant	NTNG2	GRCh38.p7	9:132216011	CCTGCCACATGGAAA[-/C/CC]CAGCCACTTCCTAGG	84628
rs148844754	snp	C/T	0.0356815	0.128715	intron-variant	NTNG2	GRCh38.p7	9:132190532	CGCCCCTCCACGGCC[C/T]CCTTAGTCAGGGGCC	84628
rs148912488	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210509	AGTTCATAGTAGGTA[A/T]AGCCAAAGGTACTTT	84628
rs148958066	snp	A/G	0.0015004	0.0273486	synonymous-codon	NTNG2	GRCh38.p7	9:132166858	GCTGGCGCTCTTCCT[A/G]CACTGCCTCCCTCTG	84628
rs148959984	snp	G/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132172479	CATGAGCACGGTGCT[G/T]GGCACATAGTAGTTG	84628
rs148964699	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243101	CCAAAAAAGAAATCC[A/G]GAGTGTATTGGCCCT	84628
rs149009251	snp	C/G	0.000779119	0.0197219	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241031	CACGCACTACTGGCG[C/G]CAGGGCTGCTACCGT	84628
rs149058817	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132225707	GTTCCATTTGTTTGC[A/G]TGTTTGATTTTACAG	84628
rs149116022	snp	A/G	0.0356815	0.128715	intron-variant	NTNG2	GRCh38.p7	9:132174885	TGAGATCGTCCCACT[A/G]CACTCCAGCCTGGGC	84628
rs149159019	snp	A/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132167534	CACTGAGCTGGCCCT[A/T]TGCATGGGGAGGTTT	84628
rs149168815	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205337	CTGAGGACATGATGC[G/T]AAGTGAAATAAGCCA	84628
rs149217099	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132231854	TAGCCTGGGTCCCTG[A/C]CTCTCTTGGGGTGGG	84628
rs149320221	in-del	-/CT			intron-variant	NTNG2	GRCh38.p7	9:132172718	GAGGCAGGATCAGGG[-/CT]GTATTTTTTTTTTTT	84628
rs149321801	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132198672	TCTGTTACCTGGGAC[A/G]TTATTGGATACCTGG	84628
rs149331952	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132238793	CATCCTTCAGCGAGC[A/G]CTTGGCCCTGGTGCC	84628
rs149535525	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163725	ACGGCGAGGGCGCAG[C/T]AGGCAACTCCAAGAG	84628
rs149602250	snp	A/G	0.0119091	0.0762411	intron-variant	NTNG2	GRCh38.p7	9:132219446	GATGTGGTGGTGGGT[A/G]CCTGTAATCCCAGCT	84628
rs149667458	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231203	GTTCCCCAGGAGGGC[A/G]AGGGCGACATGGCGC	84628
rs149711678	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184099	ACCCACCCCCAACGA[C/T]GAGCCAGGGTTCATC	84628
rs149810168	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208967	CAAGGGGTCTCCTTC[A/G]TTCTCACTGTGCCTC	84628
rs149825104	snp	A/C	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132236069	TCCCACGACAGGAAC[A/C]CCCCTCTCCAGCTGC	84628
rs149827815	snp	A/G	0.00835141	0.0640778	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166664	GGCCTTTTGGAAACA[A/G]CAAGTTCCTCGCTGT	84628
rs149922563	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221620	TGGGGCTCAGCCAGC[A/G]AGTTGAAGAGGCCGG	84628
rs150068857	snp	C/G	0.00993419	0.0697739	intron-variant	NTNG2	GRCh38.p7	9:132211981	ATGAACTTACATGAA[C/G]AAAGAAGTCTTACTA	84628
rs150125487	snp	C/T	0.0232847	0.105357	intron-variant	NTNG2	GRCh38.p7	9:132181494	CCTGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC	84628
rs150145391	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238437	CAGCGAGTCAGAAGC[C/T]GGGCCAGGACCAGGG	84628
rs150179081	snp	A/G	0.0225045	0.103662	intron-variant	NTNG2	GRCh38.p7	9:132177123	TCCCAAGTAGCTGGG[A/G]TTACAGGTACACACC	84628
rs150187935	snp	A/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132227474	GAGTGATGGGGTGGG[A/T]CCCCCACTTCAGGTG	84628
rs150239982	snp	C/T	0.0103295	0.0711199	intron-variant	NTNG2	GRCh38.p7	9:132222703	CTCCCACGGCCCACC[C/T]AGGACCTGCAGGATT	84628
rs150387807	snp	A/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213644	GCCACCGTAAGATCT[A/G/T]GGATTTGCTTTAGGT	84628
rs150397945	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132191967	TGAAATATTTAAAGA[A/G]GCAGCTACTACTTCT	84628
rs150408471	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132233251	TGGCTGGGAGGCCAG[A/G]TACTCTCCATATCAC	84628
rs150507312	snp	C/T	9.8301e-05	0.00701005	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230552	GGGGCAGCCAGCTCA[C/T]GCCCGTCTCTCTCCC	84628
rs150515848	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173740	GGAGCACCATGCTGC[A/G]GATGAGATGGATGGA	84628
rs150560929	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224359	ACTCTGTGTTGGACA[C/T]TTCAGTGGGTTTTGC	84628
rs150629706	snp	A/G/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132221537	CCCCACACAGTGCCA[A/G/T]CTCCTCCCTGCAGCC	84628
rs150646325	in-del	-/T	0.0341408	0.126114	intron-variant	NTNG2	GRCh38.p7	9:132183107	GGCCTGCCTCGGCTC[-/T]TCTCAGAGCCTCTCT	84628
rs150671993	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132176317	GTTTCCATCGCCCCA[A/G]TAGAAAACCCTGCAC	84628
rs150682279	snp	C/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132216954	CAGGCATGGGGGCAT[C/G]TGGCTTAGTGGCCCC	84628
rs150719334	snp	A/G	1.64923e-05	0.00287156	missense	NTNG2	GRCh38.p7	9:132166979	CGCCTGAAGGACTAC[A/G]TCAAGGTGAAGGTGG	84628
rs150723669	in-del	-/TG			intron-variant	NTNG2	GRCh38.p7	9:132181961	GAGGCGGCTGTCATC[-/TG]TGTGTGTGTGTGCGT	84628
rs150767466	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160663	GGGCGGGGCACTGAG[A/G]TGCCATGTCTTGCTC	84628
rs150840129	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132183558	CCAGCCCGTCACCTC[C/T]AGGGCTTGTCATCTG	84628
rs150887139	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240054	ATGGTTGCCCCTGTC[A/G]TCAGTAGAGGCCAGG	84628
rs150894335	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132178928	GACTGTGCCACTGCA[C/T]TCCAGCCTGCACAAC	84628
rs150949918	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222617	CCAGAGACGTCCTTC[A/G]TCCTGGGAACTGAGC	84628
rs150993217	snp	C/G	0.0225045	0.103662	intron-variant	NTNG2	GRCh38.p7	9:132177063	GTTGTGATCTTGGCT[C/G]ACTGCAACCTTCACC	84628
rs151044775	in-del	-/GATG			intron-variant	NTNG2	GRCh38.p7	9:132173846	CCATGCTGCGGATGA[-/GATG]GATGGATGGACAGAC	84628
rs151045491	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132208214	AGAAACCTGAAGGGG[G/T]AACGGGGGCACGGCA	84628
rs151089458	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166085	ATCTCAGAAACTTCA[C/T]AATAAGTTGCCGATG	84628
rs151099758	snp	A/G	0.0228947	0.104514	intron-variant	NTNG2	GRCh38.p7	9:132204405	AGATGGACGGACACC[A/G]GACTAGAATAGAAAC	84628
rs151162836	snp	A/G	0.0193772	0.0965046	intron-variant	NTNG2	GRCh38.p7	9:132186465	TGGCAATGCCTCCCC[A/G]CCCACCACACTCTGG	84628
rs151209525	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180992	CTTTCGGTCAATCAT[C/T]TGGCCTGAGCAGGTT	84628
rs151252497	snp	C/T	1.81013e-05	0.00300838	synonymous-codon	NTNG2	GRCh38.p7	9:132226882	CGCCAACCTGTGCTC[C/T]ATGCGCGAGGGCAGC	84628
rs180673893	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181355	AGACGGAGTCTTGCT[C/T]TGTCACCCAGGCTGG	84628
rs180682727	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193148	AGGAAGATGAAGAGA[A/G]ACCAGGGAAAAGGTG	84628
rs180695530	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132170689	AGCCACCCGAGACTC[A/G]GGGGTGAGCTGACGA	84628
rs181068191	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203766	GGCAGGGGCAAGATA[A/G]CAAAACAGCCCAGCC	84628
rs181078570	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132238287	CCTTGCCCCAGGCAG[C/T]CACGGGCTTGTCTGG	84628
rs181106651	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132204198	GAGCTGGGCCTGGAC[A/G]GGCAGATCTGAGCTC	84628
rs181118044	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238788	GTGGGCATCCTTCAG[C/T]GAGCGCTTGGCCCTG	84628
rs181127186	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132221531	GCCTTTCCCCACACA[A/G]TGCCAGCTCCTCCCT	84628
rs181224332	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228994	CAGTCACCACCTCCA[A/G]TCTAGCCAGCGATGG	84628
rs181228388	snp	A/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132193843	AAAGTCCAAGATGAA[A/G]TTGTTGGCAGGTTTG	84628
rs181244394	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132207694	ACCTATGACATGCTG[A/G]ACACAAGCAGGGTGC	84628
rs181247237	snp	C/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132212936	ATCTCTCCCAACCCC[C/G]CAAAGAAGACCAAGA	84628
rs181254242	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224381	GGGTTTTGCCATATG[C/T]ATAATGCCACATATC	84628
rs181258555	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165765	GACCCCCAAGCCGGG[A/G]CACTTCTGCTGAACT	84628
rs181266828	snp	C/T	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132187429	TCCAGGGCCTGTGCA[C/T]GAAGAGAATCTGGAA	84628
rs181267285	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171324	GCCTTGCCCACCTCA[A/C]CGACTTCCTGGGAGA	84628
rs181447552	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216122	GACTGTCTGGCCACC[A/G]CGCTACCTGGTGCTG	84628
rs181448577	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132175881	GTACATTCTGGGAGT[C/T]TAGGGAAATCCAGAT	84628
rs181476703	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167828	AGTGTGTGGGCCGAG[C/G]CTGATGCCATTGCGA	84628
rs181841248	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233588	GACATTAGGGGAGGA[A/G]GTGGCTCCAATGTGA	84628
rs181855412	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165214	GATTCTCCGGGTGAC[C/G]TATCCAGTGTCTGGA	84628
rs181856753	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216756	GGAAAATTGATCCCA[C/G]AGAAGAAGGGGAAAT	84628
rs181884569	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132198927	TGGTACCTGGGACAT[A/G]ACCTGGTTCTTGGAA	84628
rs181891427	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132208364	CCCTGCAGCCCCGGG[A/G]GGAAGTTGGTTTTGG	84628
rs181896871	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232974	GGGGCAGCACACCCC[A/T]CCTCTTTCTACATCC	84628
rs181964277	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220207	TCATTTTATTATTGA[A/G]TTATAAGTGTTCATT	84628
rs181971008	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171965	ATGGGAAAGTGAGAT[A/G]ACTAGAGATAAATTA	84628
rs181973855	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213286	GAGATCGTGCCACTG[C/T]ACTCCAGCCTCCAGC	84628
rs181975610	snp	C/G	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237522	ATTGAAGAATTCCAA[C/G]GTAAGAGGATGGACC	84628
rs181976641	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194829	GCCAGGGGACCTGTC[C/T]TTCACCCTAGAGGAT	84628
rs182024929	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132223737	CCTGCCCTGGTCCAG[A/G]CCTCTATTCGCAGGA	84628
rs182053580	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186757	GCGAAGCCCGCGGAT[G/T]CCCACCGCCTCTCCC	84628
rs182185355	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132188489	CACCTCAGCTGCTGC[C/T]GAGCCGCATGACCCT	84628
rs182189633	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132224662	TTCTACTAAACCCAT[C/T]GCTCTGCAATTTGCT	84628
rs182218308	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132180692	TCAGGGAGACGGAGA[A/G]AGAGAGAAAGAGAAA	84628
rs182321839	snp	A/C	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132207568	CAGCTTAACTTACAT[A/C]CTCATCCACATCCAC	84628
rs182329363	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132176582	CATATTTTGTGTATC[C/G]GTTTCCTAACTGATG	84628
rs182424083	snp	G/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229858	CTTTTGCAACTCTGA[G/T]GAATCTCACCCAGGG	84628
rs182459683	snp	A/G	0.0162398	0.0886349	intron-variant	NTNG2	GRCh38.p7	9:132184269	TCAGGGGCAGGCCCC[A/G]TCCATCGGGTGCTGT	84628
rs182469379	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195306	CTCTTTTTTTTGTTT[C/T]CGTTTTTGTTTTTGT	84628
rs182473701	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182257	GAAGGAGTGGGGGAA[A/G]AAATTGCACCCAACA	84628
rs182476456	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162521	CCCCGGGTCCTTTCC[A/G]TCGTGTGTGTGAGAG	84628
rs182479109	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132213443	CCACGGCCACCCACC[A/G]GCTGGGGAGGAGAAA	84628
rs182479878	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203173	ATGTCTGCAGAGGCT[A/G]GAAACACAACTTACG	84628
rs182686832	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226140	TCGTGAAATGCTTCT[A/G]TAAAAAGAAGCTTCC	84628
rs182697006	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242749	TATTCACTGTCCCCT[A/G]CAAGGGGGACGGGGC	84628
rs182699713	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191344	TACGAAGCTGCTGTT[C/T]CAAAATAATCGCTCC	84628
rs182712769	snp	C/T	0.0146672	0.084371	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209004	TTATGGCGTGGCCGC[C/T]TGCGTGGCTCGGGCT	84628
rs182716263	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132168743	GGAGGGTTCTCCACA[C/T]GCTCTCGGGCACGGT	84628
rs182741292	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132205916	GGTGATAAATATATA[C/T]GTATATTTTAGCACA	84628
rs182869991	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230178	CTTCTTAGACAGGAA[C/G]ACTCCATACGATGTC	84628
rs182901359	snp	C/T	0.030665	0.119967	intron-variant	NTNG2	GRCh38.p7	9:132195552	CAGGATGGTGTTGAT[C/T]TCCTGACCTCGTGAT	84628
rs183013001	snp	A/G	0.0138799	0.0821421	intron-variant	NTNG2	GRCh38.p7	9:132221973	TCAGGCCAGCAGTGC[A/G]GAGCACAGCCCCGGT	84628
rs183025207	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132199914	AGGAGATGAAAGCAG[C/G]CTTTACCTCCCAAAA	84628
rs183029434	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234939	CTTCAAGAAGCGGAA[A/G]ACAGCAGCGCTCCCC	84628
rs183034334	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217190	TCACGAGGATTTGTT[C/T]AATAATGCATGGCGT	84628
rs183045689	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132178871	TGAGGCAGAAGAATT[G/T]CTTGAACCTGGGAGG	84628
rs183057473	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132177247	CCGCCTGGGCCTCCC[A/G]AAGTGCTGGGACCAC	84628
rs183112777	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235510	CAATTCCTTTGGCCA[A/G]TGTAGACAGAGCCTC	84628
rs183156270	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132213802	AGTAGTCTAACTTTA[G/T]CCCCCAAGGTACCAG	84628
rs183192339	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173363	GCCCAGGGAGTGAGA[A/C]CCTTGCTTCTGACTT	84628
rs183239527	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214708	GCCACACGGGTGAGC[C/T]GGGTAGCAGGTGGGC	84628
rs183244483	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132196121	CTAAAGTCCATAATT[C/T]ACATGAGAGTTCACT	84628
rs183263991	snp	A/G	0.00432314	0.0462912	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231420	CTTCTGGGGTGCACC[A/G]TCACCCTCCACCAGG	84628
rs183269101	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174556	TGGACACAACCTCGA[A/T]GGACGTGTGTACAAA	84628
rs183305112	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189343	ATGAAGACCCAAAAC[A/T]TTGGTGAACATCTAT	84628
rs183310774	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233964	TTTGAACTCAGGGCT[C/T]GCCAACTCAGCCACC	84628
rs183317108	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132168236	CACTGGGCAGTGCTC[C/T]GGAGGCCGTCCCTGG	84628
rs183333743	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132199288	GGGGTTTCCGAGACC[A/G]CCCTCAGGCTCCATG	84628
rs183602828	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132211571	AAAGGCTGGGTCTCT[C/T]GGGCTGGCCTAGGGG	84628
rs183614163	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193700	CTGAGCCATTCCTCC[C/T]GGCCTGTTCCCTCTT	84628
rs183616048	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228596	AGTCTCTCACTCTGT[C/T]GTCCAGGCTGGAGTG	84628
rs183721622	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207614	TGTAAGGTCACATTC[A/G]TAGGCACTGGGGGTC	84628
rs183722112	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132201078	CAACTGTTCAAGGAC[A/C]CTGCCTTACCTTTCA	84628
rs183734241	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132225549	TGCTTGGATTATAGG[C/T]GTGCACCACCACGCC	84628
rs183741033	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132186763	CCCGCGGATGCCCAC[C/T]GCCTCTCCCCCAGGC	84628
rs183745351	snp	C/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132232130	AGGTGCTGGGGGCAG[C/G/T]GAGGCCATCCTGACA	84628
rs183751802	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132165387	TTGTAACCCATTTAT[A/T]GACCTACCCTCTAAG	84628
rs183753318	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132215453	GGTGTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	84628
rs183793411	snp	C/T	0.000472569	0.0153643	synonymous-codon	NTNG2	GRCh38.p7	9:132226927	CGAGCACAACACCAC[C/T]GGCCCCGACTGCGGC	84628
rs183924806	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132182767	GGCCTCAAGCCCAGC[A/G]GGCAGCTATGACCCC	84628
rs183929663	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132221655	TCTTCTCCTGTTCCC[A/G]AGGAAGACAGGACTG	84628
rs183945460	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218348	ATGACATGTCATTCA[A/G]GGGATTGCTGTGAAG	84628
rs183971330	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179317	TCTACTTCCCAGCCT[A/G]CTTAGGTGAGCTCCC	84628
rs183976597	snp	A/T	0.0146672	0.084371	intron-variant	NTNG2	GRCh38.p7	9:132208721	TTCTGGAGGGGAATT[A/T]TTTTTTTATTTCTTA	84628
rs184020784	snp	A/G	0.00517822	0.0506191	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243657	GCACTGGCTTCTGCC[A/G]CCACACCTGTTCTTT	84628
rs184024255	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132222985	CAGGCATGGTGGCAC[A/G]CGACTGTGGTCCCAG	84628
rs184051648	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132163816	GAGTTCAGAAATCCT[A/G]ATAAAATCTAATTTT	84628
rs184059216	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132206559	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	84628
rs184064827	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185058	GAAGGGTGTCTGGCT[A/G]CAGGCTGAGAATGGG	84628
rs184077463	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132205393	ATTCTGCTTACCCGA[C/T]GTCCCCAGAGTCGTC	84628
rs184103299	snp	A/G	0.00835141	0.0640778	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159715	GGCACATATCTTTAC[A/G]TATGGGTCACTGAAA	84628
rs184457487	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132235766	AGACCCCGGGGAAGC[A/G]CCCTCTTAGACTCGT	84628
rs184567380	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211065	TCACAGACGCGGACC[A/C]ACAGGGTGAGCGGAG	84628
rs184585499	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132232461	AGACAGGCATGGAAA[C/G]CTGATTCTCGCTCCC	84628
rs184587919	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132228230	CAAAGCTGAGAGCCA[C/T]GTGCAGAGGCCATGA	84628
rs184597220	snp	G/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132192858	CTGTTGACTGAGCTC[G/T]CTCCACAGCAGGCGA	84628
rs184599100	snp	A/C	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132197794	GCACACCTCTGCACG[A/C]ATTGAGGAAATGGGC	84628
rs184604868	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132224334	GGGCCTGTTATTTAC[A/G]TTAGGACTCACTCTG	84628
rs184612750	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132197116	GCTCAGGGGCCGGGC[A/G]CAGTGGCTCACGTCT	84628
rs184634387	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132236511	CTTCCAGCTCACATG[C/T]TCAAATTTCCTCCAG	84628
rs184638418	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132220068	CTCATTATGGCTTTG[G/T]TGTGCATTTCCCTGA	84628
rs184673072	snp	A/C/G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132203045	GTGGGAGAGGGAAGT[A/C/G/T]GGGGAGGCTTGGGGT	84628
rs184675600	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180508	GTTCTGGGGCTGGCA[C/T]CGTCCTGGGGCTCAG	84628
rs184745185	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175306	GTCTGGCTCCTGACC[A/G/T]CTCGCTAGGGTTAGG	84628
rs184749373	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215916	ATAGCTGACGTTTCC[A/G]GAGGGCATGCTCTGT	84628
rs184787287	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132180138	CATTCCACTTCCCTC[C/T]TGCTGCCCAAGTCAT	84628
rs184787472	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132219220	GACTCTGTCTCAAAA[C/T]AAAAAAAAAAAAGAA	84628
rs184885411	snp	A/G	0.0314385	0.121371	intron-variant	NTNG2	GRCh38.p7	9:132202114	CCACCTGGAGCTCAG[A/G]TAGCCTGTATGATGG	84628
rs184891914	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170745	ACTGCCCAGGCAGCA[A/G]GGTGCCAAGGGAATC	84628
rs185059704	snp	A/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132181752	TCTTAAGGTAGAGCT[A/T]GTATTTAGATCCGTT	84628
rs185149476	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223171	CCTAACCATTCTGCA[C/G]GATAATTCGAGGACA	84628
rs185241637	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230115	GACGCACTCCACCCG[C/T]GGCAGCCGCTCCCAT	84628
rs185284245	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244426	CTCAAGTGAGCCTCC[A/G]GCCTTGGCCTCCCGA	84628
rs185298568	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178031	TGGATATTCTGCACT[A/G]TAGAAACGATTACTC	84628
rs185298583	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207755	TCCCGTAGTGGGAGA[A/G]CAGAAATCAACAAAC	84628
rs185303439	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210143	TGTCCTGAGTAAAGA[A/G]TGGCACATCACGGTG	84628
rs185306204	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187699	AGAATCTCCGTTTCC[A/G]CTTTGTTAATAATTT	84628
rs185314800	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132224586	TTCCCAGCTCAGAGC[C/T]CCTGCCACATAACAG	84628
rs185340484	snp	G/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132169164	GGGGAAGGCAGGGGA[G/T]AAAGAACAGTCCCTC	84628
rs185389450	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233844	AGGCTTAGGAAGAAG[C/T]AGCTGGATTTTATGA	84628
rs185408043	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237607	ACGGTGCAGGATAGA[A/G]GACCGATGCCTGGCT	84628
rs185444479	snp	C/G	0.0115144	0.0749975	intron-variant	NTNG2	GRCh38.p7	9:132192158	GCAAACCTTCACCCC[C/G]ACTCAGAGGAGACAC	84628
rs185521283	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132220413	TCCTGTCTAAGAAAC[A/C]ATTGCTTAATTCAAG	84628
rs185558622	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186229	CCTGTCTGAGACAGA[C/T]GCCCATGTGTCTGGT	84628
rs185681661	snp	A/G	0.00178746	0.0298418	intron-variant	NTNG2	GRCh38.p7	9:132239071	CCTGAATGCTCGCTG[A/G]CCATTGGTATTTCTC	84628
rs185700210	snp	C/T	0.0364509	0.129988	intron-variant	NTNG2	GRCh38.p7	9:132206591	AGAATCACTTGAACC[C/T]AGAAGGCGGAGGTTG	84628
rs185706484	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164762	TGGCTGGGTTCTCGT[C/T]CATCTCCATCAGCAG	84628
rs185904984	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221304	AGAACATCTGCTGGA[C/T]AGAGACATGGAGAGA	84628
rs185910085	snp	A/G	0.0240643	0.107019	intron-variant	NTNG2	GRCh38.p7	9:132195372	GGAGCGCAGTGGCGC[A/G]ATCTCGGCTTACTGC	84628
rs185944786	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204262	CTTCCCCAGACCCTG[C/T]GGGGGTCTAGCTGCT	84628
rs185954469	snp	A/G	0.000209096	0.0102227	intron-variant	NTNG2	GRCh38.p7	9:132238946	TCTCTTCCTGAATCC[A/G]ATGGAAGGGTGGGAG	84628
rs185962521	snp	A/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132221564	AGCCCTGCTAGACAG[A/G]GCAATTCTCTCCTTT	84628
rs185973555	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182264	TGGGGGAAAAAATTG[C/T]ACCCAACAATGGACA	84628
rs186020703	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213500	CCCTCCCAGGGCAGC[A/G]TCATTCCTCACTGCA	84628
rs186037680	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216823	GCCCAGGTCCAGATC[A/C]AGGCAGAGGCTGGTG	84628
rs186049242	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233503	GGACCCCCTCAGTGA[A/G]CAGAAGGCACACCCT	84628
rs186049569	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132238369	GTGGGGTGCAGGAGG[C/T]GGCAGGACATGGTGG	84628
rs186077742	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132176835	AATGCCAGTTTCTCC[A/G]AATCCTTGTCAACAC	84628
rs186084602	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216635	AAATCATCCTTTCTG[A/T]TGGATGAGCTGAAAA	84628
rs186086623	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175984	CTCAGCATAGCAATA[A/G]TCATTTTAAAAAAGA	84628
rs186092455	snp	C/G	1.66241e-05	0.00288302	missense	NTNG2	GRCh38.p7	9:132198047	CTCATGTTCGACAAG[C/G]AGGAGGAGGGCCTGG	84628
rs186177208	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132234528	ATCCTGAATACCCCC[A/G]AGTGCCTCCCAACAG	84628
rs186192078	snp	G/T	0.0123036	0.0774623	intron-variant	NTNG2	GRCh38.p7	9:132199356	TATATTCACAGTTAT[G/T]GTTTATTACAATGAA	84628
rs186203189	snp	A/C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132198985	ACTTCTTGAGATGTT[A/C/G]CTTGGTTTCCAGGAG	84628
rs186208623	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166699	AAAGCTTCAGTGCTC[A/G]GGTCCCTGGGACACC	84628
rs186289583	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229960	ATTCAGGTCAGGCCT[C/T]GCCCACTCTCGGCTA	84628
rs186301491	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217548	AGAGATAGTCATAGT[A/T]TACTCTGCATAAGGT	84628
rs186308157	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132172760	TTGGAGTCAAAGTCT[C/T]GCTCTGTCGCCCAGG	84628
rs186308207	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213304	TCCAGCCTCCAGCCT[A/G]GGCGATGACAGAGTA	84628
rs186314273	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195273	TTAGTGGGGGATATT[G/T]GAGGTTTTGGGGGAT	84628
rs186703134	snp	A/C	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132222891	TGGGCAGATTGCTTG[A/C]ACTTCAACCAGGAGT	84628
rs186715690	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132225065	GCTGGGATTACAGGT[A/G]CACCATCACACTTGG	84628
rs186720107	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132189164	TCACTACAGCCTCGA[C/T]CTCCTGGGCCCAAGG	84628
rs186739195	snp	A/G	0.0166325	0.0896639	intron-variant	NTNG2	GRCh38.p7	9:132184690	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	84628
rs186740936	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206066	TCCACAAAATGGAGA[A/C]AATCACCCTGGAGTT	84628
rs186754629	snp	C/G/T	0.0193772	0.0965046	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162906	GAGCGGCGCGCAGGT[C/G/T]GGGGGAGCAGAGGCG	84628
rs186851585	snp	C/T	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132226078	AGTTCTGGGCTGGTG[C/T]GGCTCAGTGCCTGGA	84628
rs186879516	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132168381	CTCTGGGTTTGTGGT[A/G]GGGCTGACCCGGTGC	84628
rs186887840	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132189991	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG	84628
rs186896530	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212984	TTCATGACGTCTTGA[C/T]TCAGGCCTGGGCATA	84628
rs186915858	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171391	CAGAGACTGTAAGTT[A/C]TTTTCTAGTGTGAGG	84628
rs186941026	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132208596	GTTGCTGAGTAGCTG[A/G]TGGGAGCAGGCGGTG	84628
rs186950740	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168132	GGGGTGACGGGTAAA[G/T]GCATCTGGCCAAGGT	84628
rs186993009	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209272	GCCGTCTTCCAGCGC[A/G]GCTGTGCACTGGAGG	84628
rs187051098	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229400	AACTTCCCTCCATCC[A/G]CTCCAAGTCTCTCCC	84628
rs187054176	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203269	TATTTGAGCCTGGGA[A/G]GTTGAGGCTGCAGTG	84628
rs187095057	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193866	CAGGTTTGGTTTCTG[A/G]AGAGGCCTCTCTCCC	84628
rs187234420	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132181064	TTGGTTCCCTGTAAT[C/T]GTCTGGTCCAATTGT	84628
rs187310370	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200001	TTTGGCAGATAATAT[A/G]CCAGTCTGTGGGGGC	84628
rs187313559	snp	G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132235179	AGGCTCCGGTCCCTG[G/T]ATTGCGGCTGGACAG	84628
rs187332456	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132226573	CATCACTCTCCCCAA[C/G]TGAGATGTGAGGAAT	84628
rs187335632	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132178892	ACCTGGGAGGCGGAG[A/G]CAGAGGTTGCAGTGA	84628
rs187540729	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132223075	GCCGAGATTGTGCCA[C/T]GGCACTCCAGCCTGG	84628
rs187542900	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174561	ACAACCTCGAAGGAC[A/G]TGTGTACAAATAAGA	84628
rs187549879	snp	A/C			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243884	TCCCACCCCCAGCAC[A/C]CTGCTGACCCGGAAG	84628
rs187576531	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132206560	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	84628
rs187650653	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132179404	GAGGGGATCAAGAGC[A/G]TCCCCTAAGCCCATC	84628
rs187656585	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218381	CTAATGTTCTAATTC[C/G]GGTGGCACTCTCAGA	84628
rs187768700	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242906	GGAATCCACAACACA[G/T]CCTTAAAGAAACGGT	84628
rs187800446	snp	A/G	0.0126979	0.078662	intron-variant	NTNG2	GRCh38.p7	9:132168756	CACGCTCTCGGGCAC[A/G]GTCAACCTCTGTCTC	84628
rs187839454	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173130	GTTCTGTGGGATTTG[C/T]GATTGGATGAAGCCG	84628
rs187898043	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235565	GGGGCCTGTGGGGTG[C/T]GGGGCTGTGATGCCT	84628
rs187918973	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201778	TTTCTTGTTTAATCA[A/G]TAGCCGTTTAATTCC	84628
rs187931239	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132214800	TGTTTTTTAGGGTAA[A/G]TATGTCCCAAATATT	84628
rs187939771	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196742	CACCACTGGGTGTCC[A/G]ATGATTCCGTTCAAT	84628
rs187946271	snp	A/C	0.00119737	0.0244387	intron-variant, missense	NTNG2	GRCh38.p7	9:132231481	TGTCCCTCCCGGACC[A/C]AGGGGGCCCCTGGCT	84628
rs188035354	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132207632	GGCACTGGGGGTCAG[A/G]ATGTCAACATATCTT	84628
rs188053396	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224340	GTTATTTACATTAGG[A/C]CTCACTCTGTGTTGG	84628
rs188057177	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165524	TTAAATTTGCCATTT[C/T]AGATTGTGCCTATGA	84628
rs188063581	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187277	TGCCTGAGTAATTGC[C/T]TGGAGCTGGGAGGAA	84628
rs188066249	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191355	TGTTTCAAAATAATC[A/G]CTCCCATTTGGAGAC	84628
rs188131086	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132235927	TGAGGGAGCGGCCTG[A/G]TAGAGCAGGTCTACC	84628
rs188184999	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132211077	ACCCACAGGGTGAGC[A/G]GAGGCCTCCGCAGCA	84628
rs188200716	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132228437	AAACCCTTTCCTGAG[A/G]TCTCTCTTTAGTGGC	84628
rs188209307	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170242	AGAACTGAATTGTAA[A/T]TTCCAGCCTTGCAAG	84628
rs188215639	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193062	CTTTGAGGGATACCC[G/T]GTCCCCCGCCACAAT	84628
rs188279878	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132227378	ACAGGGAAACCCGAG[A/G]GGAGCTGCTCAGCAG	84628
rs188309662	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192328	AGGTGCAATGGCTCA[C/T]GCCTGTAATCCCAGC	84628
rs188432023	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132214014	TTCAGAGCCATTGCC[C/G]TGAACACTCTGAAAT	84628
rs188452078	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219432	ACAAAAATTAGCTAG[A/G]TGTGGTGGTGGGTGC	84628
rs188607340	snp	C/T	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132169206	ACATGGGCAAGTCCT[C/T]GGCGTCTCGCCACCT	84628
rs188610348	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160323	AAGCCCTGCCTCCCC[A/G]GCCACAATCCTTAGC	84628
rs188707314	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228736	CTAATTTTCGTGTTT[C/T]TTTCAGAGAAAAGGT	84628
rs188727530	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164495	CTACCTGTTAGTGAA[C/T]AGTTAGGAGTCGACT	84628
rs188733790	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230468	TGCTCTTGAGGGAGC[A/G]ACACCTCCAGGTGCT	84628
rs188750038	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132195563	TGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC	84628
rs188867265	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180228	CATTTTCCCTTGGCC[A/G]AAGCAGAAGTCTGCT	84628
rs188871596	snp	A/G	0.0146672	0.084371	intron-variant	NTNG2	GRCh38.p7	9:132202668	TATGGTGCTTGGAGC[A/G]GGAGGGGCCTCCGCC	84628
rs188872343	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132183048	TTCCAGCCTGAAGCA[C/T]CTTGTCGTCTTAAAA	84628
rs188874648	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132221683	CTGATAGGAGGGGCT[A/G]GCCAGGATGGAGCCT	84628
rs188952585	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132236609	CATGTTTAGAGAGGG[C/T]CTGAGGCTCGGTTCC	84628
rs188960564	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220161	AATGTCTGTGCTGAT[C/T]CTTTCCTCATTTTAA	84628
rs188961132	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132241574	ACAGGGTGAAAGGAG[C/G]CTCCAGGCGCGTGGA	84628
rs188992914	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203091	ATGAGGCCATTCCTG[C/T]ACCCACCCCAGGTAC	84628
rs188997202	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180686	TCTGCTTCAGGGAGA[C/T]GGAGAGAGAGAGAAA	84628
rs189077460	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197355	GATCGCCCCACTGCA[C/T]TCCATCCTGGGAAAC	84628
rs189087972	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232231	CCTGTCCCCACCTGG[A/C]CCCCAGGGCCTCTCT	84628
rs189097898	snp	C/T	0.00155739	0.0278616	intron-variant	NTNG2	GRCh38.p7	9:132197941	ATCCAGCACCCACCC[C/T]TCCCTTCTCCTCTCC	84628
rs189112423	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175590	GGGAACCGGTCTGTT[C/T]GGCTTTGGTTTGCAG	84628
rs189177739	snp	A/C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220781	GAGTTTTCTAGTTTG[A/C/T]AGCTCTTTGATCCAT	84628
rs189199308	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132181312	GGTCTTAAACTCCTG[A/G]GCTCACTTTCTTTTT	84628
rs189389777	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174865	AGGTGGGGTTTGTAG[A/T]GAACTGAGATCGTCC	84628
rs189480972	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132238144	TTCTTGCTGGAGGGT[A/G]GGTGGGTGGGTGAGT	84628
rs189495189	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132203464	GGGGAGAAATGGAGA[C/T]AGCAGGCGCCTCACA	84628
rs189593088	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233515	TGAGCAGAAGGCACA[A/C]CCTCCCTCTCGGCAA	84628
rs189623485	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132176068	GTTAAACAACGTTTT[G/T]GTGGGTGCAGTGGCT	84628
rs189624441	snp	A/G	6.82454e-05	0.00584107	missense	NTNG2	GRCh38.p7	9:132198516	CCGACCTGCGCATGC[A/G]GCTGCTGCGCCCGGC	84628
rs189684137	snp	G/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132226114	GCATTCATCAGGGAC[G/T]GCAAATTCTCTCGTG	84628
rs189715350	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168563	AGAGAGAGAGGGAGG[A/G]AGAGAGGGAAGGAGA	84628
rs189717452	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208975	CTCCTTCGTTCTCAC[C/T]GTGCCTCTGAGGCTT	84628
rs189723949	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132190102	GCTGGGCGTGGTGGC[A/G]GGCACCTGTAATCCC	84628
rs189766716	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211896	CAGAACCAGGTAGGC[A/G]TGCTGTATATGTGTG	84628
rs189848447	snp	C/T	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132195293	TTTTGGGGGATTTCT[C/T]TTTTTTTTGTTTTCG	84628
rs189853800	snp	C/T	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229783	CACACATCCCACTGC[C/T]AATCCCACAGCGTCC	84628
rs189862566	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213407	CACCAACCTTGAGGC[C/T]GTCCATCGTCCATCC	84628
rs190010408	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132193763	CTCCGGCCACCATAA[C/T]AAAGTAGCACACGAG	84628
rs190030575	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132216062	TCCCCAAGGCTGGTC[A/G]CCTTCCTGCCTTTGC	84628
rs190093484	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199724	TCTTCCTAGACAGGA[C/T]AGTCCAACGGCTTAT	84628
rs190139692	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132196164	CAGGTCTATGGGTTT[G/T]TTTGTTTGTTTTGTT	84628
rs190230903	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221473	TCAGAGAGACCAGAA[A/G]CACCTGCATTGACCA	84628
rs190237765	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204040	TCAAAAGGAATAAAT[A/G]TGGATTAAGGGAACA	84628
rs190247110	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232788	TCTGATCCAAGGAGA[A/C]CTGCCCCACTGATCC	84628
rs190260133	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182078	GCCCGGAGGAGTGAC[A/G]GTGTTCCCCACCCCC	84628
rs190335854	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240292	GCAGGGACAGGGCAG[A/G]GCCTTTGGATCCAAT	84628
rs190355871	snp	A/C/G	0.0150737	0.0856109	intron-variant	NTNG2	GRCh38.p7	9:132204359	TTTTCTTCCATAAAC[A/C/G]TCCTGTCCCTATTGA	84628
rs190370798	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221634	CGAGTTGAAGAGGCC[A/G]GGACATCTTCTCCTG	84628
rs190506057	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132178711	TCTGGGAGGCTGAGG[C/T]GGGCGGATTGTCTGA	84628
rs190527982	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171820	ATCCAACAATGCAGA[C/G]CTGACCGGCCCGATG	84628
rs190548414	snp	A/G	0.0364509	0.129988	intron-variant	NTNG2	GRCh38.p7	9:132206592	GAATCACTTGAACCC[A/G]GAAGGCGGAGGTTGC	84628
rs190558077	snp	A/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244494	GCCTGTCTTACTGTG[A/T]GAGAAAAAAAATAAA	84628
rs190581541	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165213	GGATTCTCCGGGTGA[C/T]GTATCCAGTGTCTGG	84628
rs190657578	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132233935	CTCAGAATTATGGAG[A/G]GGCACGGGCAGGATT	84628
rs190674329	snp	G/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132199146	TCGGAGGAAGGAAGT[G/T]CATGTGTTGGAGGTG	84628
rs190786146	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223560	CCAGTTACACATCCT[C/G]AAAACAATCTCTGAA	84628
rs190815760	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132186738	ACAGCATCCCCAAAG[C/T]GGAGCGAAGCCCGCG	84628
rs190894450	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217040	CGCAGGCAGCAGGTG[G/T]CTGTGAGATCCAGCT	84628
rs190911451	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132176924	TATCCCATTATGGTC[C/T]TGATTTGCATTTCCC	84628
rs191003799	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132235211	AAGGACACCTTCCAG[A/G]ACACTTCTGGACACA	84628
rs191015091	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229992	ATTTCTCCCCAAGCC[A/G]TGTGTCCTCAGCTGT	84628
rs191088591	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211443	TTCTCTGCACAATAT[C/G]TCTAGTGGTCTTCTA	84628
rs191108788	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132228500	CCCTTTCGTCTGTCC[C/T]GAGGGCCGCTCTCTC	84628
rs191196919	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168150	ATCTGGCCAAGGTCA[C/T]ACTCCAGGAGGTGGC	84628
rs191295475	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213598	CCTTCATCCTGCAGA[A/T]CACGCCAGCCTCCCT	84628
rs191323410	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132238672	TACCCGAGGATACCA[C/T]GGCGAGCGCCGTGAA	84628
rs191331713	snp	A/C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173359	CGGGGCCCAGGGAGT[A/C/G]AGACCCTTGCTTCTG	84628
rs191478829	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132194283	ACTCCTCCTCCCGAG[C/T]GGCACAGACAGAGCC	84628
rs191525259	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230173	CTGCACTTCTTAGAC[A/G]GGAACACTCCATACG	84628
rs191554457	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195377	GCAGTGGCGCGATCT[C/T]GGCTTACTGCAAGCT	84628
rs191593090	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132187863	GGGCCTGAGGAACAC[A/G]CAGAACTTGAGACTT	84628
rs191722166	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132182349	TCTGCCAAGGGAGGG[C/T]TCCAGGCCTGTCTGC	84628
rs191750654	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132220067	TCTCATTATGGCTTT[A/G]GTGTGCATTTCCCTG	84628
rs191756172	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132180390	GGGGGATCAAGAGAT[A/G]GCCAAAAGCAGGTGG	84628
rs191757481	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132202901	TGGATGACTGTAACC[C/T]GTTGGAACCTCAGTT	84628
rs191846587	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243223	CTCCGATGGATGTGT[C/T]ATCTCAGACCTGTTG	84628
rs191852455	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222947	GAGACCCTATCTCCA[C/T]AAAAAATAAAAATGA	84628
rs191861451	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208000	TCTCAGATACCTGGG[A/G]GGCTGAGGTGGGAGG	84628
rs191873437	snp	C/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132163199	GGAAGACGAAAAGCA[C/G]CTGCGGGGCTGCCGG	84628
rs191876657	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206392	CAACTCTTGGCCGGG[C/T]GTGGTGGCTCACGCC	84628
rs191878791	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132184722	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	84628
rs191903825	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132167816	GCGAGCTGTCTGAGT[A/G]TGTGGGCCGAGCCTG	84628
rs191933395	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174539	GAAACTGGGCATGGC[A/G/T]CTGGACACAACCTCG	84628
rs191946418	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195582	TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG	84628
rs191955940	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221855	ATGCTTCTTGGATTC[A/G]GCCGGTCTTCTATGC	84628
rs191957420	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223076	CCGAGATTGTGCCAC[A/G]GCACTCCAGCCTGGG	84628
rs191959207	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184170	CAGACCCAGTAACTT[C/T]ACTCTTTCATCGGCC	84628
rs192084635	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208615	GAGCAGGCGGTGGGA[A/G]GCATCATGGAGGACT	84628
rs192147659	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235616	TCAGCACCACCCCCT[C/T]GCATAACTTGGTTTC	84628
rs192161396	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202044	TCAGCCACCGAGCTG[C/T]CCCTAGCCCTGGCCC	84628
rs192249075	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242746	TTGTATTCACTGTCC[C/T]CTGCAAGGGGGACGG	84628
rs192292786	snp	C/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132205897	AAAGAAAAAAACATG[C/G]TAAGGTGATAAATAT	84628
rs192444856	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215346	AGCATTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	84628
rs192446091	snp	G/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132225284	GTTTTGTTTTGTTTT[G/T]TTTGGAGACAGAGTC	84628
rs192452764	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196922	CAGGTTTGATAGTTT[G/T]CTAGAACAGCTCACG	84628
rs192460512	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132232093	ACCATTGTGGCCAGA[C/T]GGCTGCAGGAACTGA	84628
rs192477340	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132174649	AAAGGGCCGGGTGCA[C/T]GGTGGCTCAAGCCTG	84628
rs192561678	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132179598	GGGAGCCTCATGAGT[C/G]AGAGACTGGGGCACA	84628
rs192608061	snp	G/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132169404	TTTTTGGAGGGGGTG[G/T]TTACTTCTAGATAGA	84628
rs192612302	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132200649	TTGTTTCACTTTGAC[A/G]GTGTGTGTGGATTCC	84628
rs192614952	snp	A/C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132192451	CAAAAATTAGCCAGG[A/C/T]GTGGTGGCGCACGCC	84628
rs192631108	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218244	TTGGATTCAAGTCCT[A/G]CGTCTGCCCCTTACC	84628
rs192691614	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132191452	AGACTCAGAGAAGTC[A/C]AGTGACTTTGTCAAG	84628
rs192716751	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160584	CAGCAGTATAACTCC[A/G]TCTCCAGTTTTCAGG	84628
rs192753362	snp	A/G	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132215876	CTCTATCACCTGTTG[A/G]CTGTTGACAATAGCA	84628
rs192824016	snp	C/T	0.0364509	0.129988	intron-variant	NTNG2	GRCh38.p7	9:132206590	GAGAATCACTTGAAC[C/T]CAGAAGGCGGAGGTT	84628
rs192824158	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164629	TCTCAGGTTGCAAAA[A/G]TAGACACCGGGCACG	84628
rs192825990	snp	A/G	0.00082515	0.0202952	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231280	CAGGGTGCCAGGCAC[A/G]GTCTCTCCTTTCAGC	84628
rs192894284	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132209660	CCAGAGCAGAGCCCG[A/G]GAGTCCGGGATGAAG	84628
rs192911094	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169069	AGAGCCTCATCCCAG[A/G]CAGCCAGCCTCAAGC	84628
rs192942666	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132232420	AGGCCAGGGCCAGAC[A/G]TCCTGCCCCCTCAGG	84628
rs192951899	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132197623	AGGTGTGGGAGGGCA[C/G]GTTGGGGTTGGTATA	84628
rs193025186	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132185763	TTTGGGTGGCCAGTG[A/G]AGCCCTGAGTAGGGA	84628
rs193119687	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132210807	CTCAGCAGAGGGAGC[A/G]TGGGGTGGGTCATTG	84628
rs193134592	snp	A/C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132179249	CTGCCCGGATGCCAC[A/C/T]TGCAGCCAGTGGGGG	84628
rs193277620	snp	A/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132227756	ACTCACATCTGCATC[A/T]TAGACCCCCTTCTGA	84628
rs199648760	in-del	-/CCT			intron-variant	NTNG2	GRCh38.p7	9:132179005	TGAGGCACATCCCCC[-/CCT]CTCATTTCCTATGAA	84628
rs199657519	snp	A/C/T	1.7999e-05	0.00299987	intron-variant	NTNG2	GRCh38.p7	9:132239020	CGTCCCTGCATGACC[A/C/T]GGGGTGAGTCCTTCC	84628
rs199932257	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132224716	CTTGGAAATCTTCCC[A/G]TATCAGAATATAGAG	84628
rs199960941	in-del	-/GAGA			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162532	TTCCGTCGTGTGTGT[-/GAGA]GTGTGTGTGTGTGTG	84628
rs200232295	in-del	-/CAG	0.0410537	0.137264	intron-variant	NTNG2	GRCh38.p7	9:132165357	AAGCTTAAAATAGCA[-/CAG]CAATAATCGTAATTG	84628
rs200267226	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132217987	GGTGTGGTCCATATC[A/G]CTCCTCAGGGCCAGT	84628
rs200296152	in-del	-/A	0.0322114	0.122752	intron-variant	NTNG2	GRCh38.p7	9:132189410	AAGTACGATTGGCTT[-/A]AAAAAAAAGGTATCA	84628
rs200302783	in-del	-/C			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243056	CCTGTTAGGAGCCTC[-/C]CCACACTGAAAGGCT	84628
rs200352273	snp	A/G	0.000232818	0.0107868	intron-variant	NTNG2	GRCh38.p7	9:132197959	CCTTCTCCTCTCCCC[A/G]CTGCAGGAGAATCCC	84628
rs200357439	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132163030	CGCCACAGGCGGCAG[C/T]GCCGGGGCAAAGGAT	84628
rs200407107	snp	C/T	0.00299549	0.0385846	synonymous-codon	NTNG2	GRCh38.p7	9:132226939	CACCGGCCCCGACTG[C/T]GGCAAGTGCAAGAAG	84628
rs200586400	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213700	ATGAAAAATGTTTTT[A/G]CCCAAAACAAAAGAA	84628
rs200589444	snp	A/G	3.30781e-05	0.00406669	missense	NTNG2	GRCh38.p7	9:132239118	GACTGCGAATGCTAC[A/G]GTCACTCCAACCGCT	84628
rs200598842	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185407	GGCCTGTCCCTCACC[C/T]CACCCCGGCACTGAA	84628
rs200666007	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132181594	TGTCGGGATTACAGG[C/T]GTGAGCCACCGTGCC	84628
rs200667359	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173993	ACAGGCAGGCAGGTC[A/G]AACCATGCTACGGAT	84628
rs200740022	in-del	-/T	0.0170251	0.090679	intron-variant	NTNG2	GRCh38.p7	9:132164128	CGTGTGCTGAGCTCG[-/T]TAATTCCCCCTGCGA	84628
rs200794330	in-del	-/AG/G	0.481703	0.0938806	intron-variant	NTNG2	GRCh38.p7	9:132219588	AAAAAAAAAAAAAAA[-/AG/G]GAAAGAAAGAAAGAA	84628
rs200827931	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174949	TGTATTTTTATTTTT[A/G]TCCTTTTTAATTCTA	84628
rs200913269	in-del	-/TC			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166008	AGCTCTCTCTCTCTC[-/TC]CTCCCCTCTTACAAT	84628
rs200941050	snp	G/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132231702	GCCACTGCGGCCACC[G/T]CAGCCATGACAGGGG	84628
rs201061734	snp	A/G/T	0.000293231	0.0121049	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230553	GGGCAGCCAGCTCAC[A/G/T]CCCGTCTCTCTCCCA	84628
rs201119955	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132208719	TTTTCTGGAGGGGAA[-/T]TTTTTTTTTATTTCT	84628
rs201159599	snp	C/G/T	0.000809967	0.0201105	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166825	CGCCTCTGCAGACTG[C/G/T]GCAGCCATGCTGCAT	84628
rs201197800	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132220462	TATGTTTCCTTCTTC[-/T]TTTTTTTTTTTTTTT	84628
rs201310857	in-del	-/A/AG			intron-variant	NTNG2	GRCh38.p7	9:132189418	TTGGCTTAAAAAAAA[-/A/AG]GGTATCATCTCCTGG	84628
rs201475380	snp	C/T	0.00399197	0.0444977	synonymous-codon	NTNG2	GRCh38.p7	9:132227017	CCATGGCTCTCCCAA[C/T]GCCTGTACGTGCCAT	84628
rs201538892	snp	A/G	0.0158469	0.0875917	intron-variant	NTNG2	GRCh38.p7	9:132163717	TTTCCCACACGGCGA[A/G]GGCGCAGCAGGCAAC	84628
rs201586879	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132223842	AAAATATGGCCCAGA[A/G]CAGGACACGCCTAAC	84628
rs201688213	in-del	-/TAT			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160487	GGTGTTCAATAAATA[-/TAT]TATTATTATTATTAC	84628
rs201951817	snp	A/G	0.00460278	0.0477515	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132241968	CGCGGCTACACCGGC[A/G]TGCGCTGCGAGCAGC	84628
rs202024962	in-del	-/AT			frameshift-variant	NTNG2	GRCh38.p7	9:132242072	ACCCTGCTCGGCTGC[-/AT]CTGCTGCTGCTGGGG	84628
rs202035291	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232811	ACTGATCCTTCCCCC[C/T]TGGGGGGTGGCATTT	84628
rs202063382	in-del	-/AGAC			intron-variant	NTNG2	GRCh38.p7	9:132173650	AGTGGATGGATGGAC[-/AGAC]GAACGGACAGACAGG	84628
rs202098758	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132195803	CAGCTAATTTTTAAA[-/T]TTTTTTTTTGTAGAT	84628
rs202147736	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132194654	GGCCCGGGCCTCAGT[A/C]CCCCCATCTGCTTAA	84628
rs202233472	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207891	GGCGGATTGCTTGAG[C/T]GCAGGAGTTCAAGAC	84628
rs367648485	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206616	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC	84628
rs367667797	in-del	-/TGTGTGTGTGTGTATGTGTG			intron-variant	NTNG2	GRCh38.p7	9:132216415	CTCTCTCTCTCTCTC[-/TGTGTGTGTGTGTATGTGTG]TGTGTGTGTGTGTGT	84628
rs367722327	snp	A/G/T	3.55393e-05	0.00421528	intron-variant	NTNG2	GRCh38.p7	9:132197962	TCTCCTCTCCCCGCT[A/G/T]CAGGAGAATCCCTAC	84628
rs367744709	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132232055	CTCCTGCCCTTCAAG[A/C]CATTGCTTGGAAGGG	84628
rs367865515	snp	A/T			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242374	CCAGTTCCTTTTTTG[A/T]CTTTCTCTCTCTCTC	84628
rs367869133	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170489	GGCAGGAAGGGCGAC[A/G]GGCAAAGGCATCTCA	84628
rs367904644	snp	C/T	0.0158469	0.0875917	intron-variant	NTNG2	GRCh38.p7	9:132223270	CCCAGGGCTGGTGGA[C/T]GCAGGGGCCGCTGTT	84628
rs367931196	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231734	CCCTACTACTCCTGT[C/T]CCCTCCACGTCCACT	84628
rs367946328	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174321	GATGAGACGGACGGA[C/T]GGACGGACAGACAGA	84628
rs367960892	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180981	ATCCGTGGTCACTTT[C/T]GGTCAATCATCTGGC	84628
rs367972655	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132196746	ACTGGGTGTCCGATG[A/C]TTCCGTTCAATTGTA	84628
rs367978169	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212191	GCCTGGTCCTTCCCT[C/T]GGGGGTGTTGGGCCT	84628
rs368038370	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132228085	GTTTCACAGTGAGTT[G/T]CATGCCAACGCCAGG	84628
rs368056950	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189607	CAAAGAGTAACCTTC[C/T]GCTTCTGTGGTTTTC	84628
rs368115112	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160211	ATTTACCGTTCATAT[C/T]TCACATATGGGGAAA	84628
rs368117190	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132209468	AGCCGGGGAGCCGGG[A/C]GGGCTGCAGCCCTGA	84628
rs368127896	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191937	GTATGATTTTTGTTG[C/T]TGTTTTAATTTTCAT	84628
rs368147282	snp	A/G	0.000198282	0.00995499	missense	NTNG2	GRCh38.p7	9:132226887	ACCTGTGCTCCATGC[A/G]CGAGGGCAGCCTGCA	84628
rs368154089	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132222178	TATTATGACCCTCAG[G/T]GGAGTGAGGTAGGAT	84628
rs368156730	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201139	GGGCCAGCTGTAGGA[C/T]CCAGACTGGGACTGT	84628
rs368159500	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177266	TGCTGGGACCACAGG[C/T]GTGAGCCACCACGCC	84628
rs368163612	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132177750	GCAACCTCCCCCTCC[C/T]GGGTTCAAGCGATTC	84628
rs368226145	snp	C/G	0.000119708	0.00773562	synonymous-codon	NTNG2	GRCh38.p7	9:132198367	GCGCTGGGCAGGCTC[C/G]AAGAAGGAGAAGCAC	84628
rs368276993	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186317	GATAGAATTTCCTGC[C/T]CCAAACATTCCTGGA	84628
rs368300529	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132188884	GACAGGATCAGATGT[A/G]GTCGCTGCCCGCATG	84628
rs368306263	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241102	GGACGGGGCAGGACC[A/G]AGGCAGTGGGCGGGG	84628
rs368395676	snp	C/T	0.000437904	0.0147905	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230515	CCCTCTGCAGGGAGG[C/T]GACACCCAGGCCCCT	84628
rs368549397	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132232392	GTGGAGGCTGTGTGT[C/G]TAGTGCAAGGCCAGG	84628
rs368565380	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132197699	GGGCTTCAAAGCAGG[A/G]GACTAACACCCAGCC	84628
rs368576254	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227815	GTCCACACTGTCTCC[A/G]TGAAATCAGAATGCC	84628
rs368606463	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232352	CCTCTGGAGCTGAGT[C/T]TGGACACCGTGGGCT	84628
rs368636615	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186567	GGCCTGGCATTTCAT[C/T]CTTGCTTTCTGACCT	84628
rs368653072	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216522	GCCGTAGGATTCTGC[A/G]GTGGGGCAGGGGTGG	84628
rs368721867	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181804	TTCAGAGAATTTAAG[C/T]CACTTGCCGAAGGCC	84628
rs368747448	snp	A/C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173951	GGAGCACCATGCTGC[A/C/G]GATGAGATGGATGGA	84628
rs368757771	snp	C/T	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240901	GCGCCCGTGCCCGTG[C/T]CCGTCCAGAGTGTAA	84628
rs368792157	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132206283	GTGAGAGCCCCTAGT[C/T]TTTGTTCCATTCTCA	84628
rs368821360	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171086	AGATTCCCAGATGCG[A/G]GCCTTGCTTGCCAAG	84628
rs368839769	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132238110	TGTCCTTCCTTGTTC[A/G]GGGGCAGCCACATTG	84628
rs368840542	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132185818	CTGAGCCCCTGTGTG[G/T]GCAGGGAGGAGGAGG	84628
rs368885959	in-del	-/GTAA			intron-variant	NTNG2	GRCh38.p7	9:132214796	TCGTTGTTTTTTAGG[-/GTAA]GTATGTCCCAAATAT	84628
rs368940462	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132221587	TCTCCTTTGGAAGAG[A/G]AGGCACTGTGCTTGT	84628
rs368940831	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132199048	CAGGACATTACCTGA[C/T]ATTACATCATAGGGA	84628
rs368946463	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132225855	ATCTGTTGGAAGAAG[A/T]GGGTCATTACTGCCG	84628
rs368954156	snp	C/G	0.0023933	0.0345097	intron-variant, missense	NTNG2	GRCh38.p7	9:132231671	CCAGAAAGACCCCGA[C/G]CCCAAAGGCCCTGTG	84628
rs368965793	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132190027	TCATGAGGTCAGGAG[A/G]TCGAGACCATCCTGG	84628
rs368973629	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132206670	AGACTCCGTCTCAAA[A/T]AAATAAATAAATAAA	84628
rs369004253	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132182669	CTTGGGTACAGAGTA[C/T]GGGTTGTCTCCCAGC	84628
rs369005262	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199733	ACAGGACAGTCCAAC[A/G]GCTTATGGATTAGAG	84628
rs369099359	snp	C/T	4.97649e-05	0.00498798	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166808	AGGGCTTCTCTGGGC[C/T]GCGCCTCTGCAGACT	84628
rs369111783	snp	A/G/T	8.28365e-05	0.00643526	synonymous-codon	NTNG2	GRCh38.p7	9:132239189	CTGCAAGCACAACAC[A/G/T]CGAGGTCAGCACTGC	84628
rs369312930	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229489	ACTCTGCCCCCACCT[C/G]GCCAGCCCATCACCC	84628
rs369320424	snp	A/G	2.43977e-05	0.0034926	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230604	TTTGGCAGTAAGTAC[A/G]CGCCTGGGGAGGGTG	84628
rs369327951	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197066	TCTTTGAGCACCTCA[A/G]TGTGTTCACCAATCC	84628
rs369344489	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132178888	TTGAACCTGGGAGGC[A/G]GAGGCAGAGGTTGCA	84628
rs369438402	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174109	GCCGCACCATGCTGC[A/G]GATGAGATGGACAGA	84628
rs369462666	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132172564	CCCCTGGACTGTGAG[C/T]TCCTCAAAGGCAGGG	84628
rs369479254	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132202673	TGCTTGGAGCGGGAG[A/G]GGCCTCCGCCCCCAC	84628
rs369501690	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132163301	CCCCGCCCGCGGCCC[A/G]CCGGGACCCACCCGG	84628
rs369516523	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194221	GAAGGGGGGCATGTG[C/T]CTGGGTGCCAGAGCC	84628
rs369536202	in-del	-/CTTGT			intron-variant	NTNG2	GRCh38.p7	9:132225229	GCCCTTTTGTTTTGT[-/CTTGT]TTTGTTTTTGTTTTT	84628
rs369562160	snp	G/T	1.87348e-05	0.00306057	intron-variant	NTNG2	GRCh38.p7	9:132198648	TGTCACCTGCAACCT[G/T]GGATGCTATCTGTTA	84628
rs369635450	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240367	CCCTGCCTCCACCCC[A/G]AGAGCCAGCACTGAG	84628
rs369664742	snp	A/T	2.56776e-05	0.00358303	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230618	CACGCCTGGGGAGGG[A/T]GGCCAGGGCCCCCAC	84628
rs369763043	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189803	AAACGCTATGCCCAA[A/C]TAATTATTTATTTTT	84628
rs369840171	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193959	CCCCAGCGTCTCATC[C/T]GGCAGCCAAACTTCT	84628
rs369843262	snp	G/T	1.64909e-05	0.00287144	missense	NTNG2	GRCh38.p7	9:132166883	CCTCTGGCCTCTGGG[G/T]ACTATGACATCTGCA	84628
rs369848311	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218246	GGATTCAAGTCCTGC[A/G]TCTGCCCCTTACCAG	84628
rs369885431	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162443	GAGTCGCCCCAGAGG[A/G]GTGTGTGAGGGTGCG	84628
rs369910752	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234948	GCGGAAAACAGCAGC[A/G]CTCCCCTGTCCCTCT	84628
rs369914807	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132178473	AGAAGGCATGCTGGG[A/G]TTGTCTAAGGCCAGA	84628
rs369959394	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132184006	GCTTCTCTGGGGCAC[A/G]AAGGATGTTCACAAA	84628
rs369972107	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216258	TGCAAACATTGAGCA[C/T]CTACTGTGTGCCAGG	84628
rs369987244	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189656	AAAAAAATTTTTTTT[C/T]TGAGACGGAGTCTCA	84628
rs370088961	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231207	GTGGGCGCCATGTCG[C/T]CCTCGCCCTCCTGGG	84628
rs370100179	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132224715	TCTTGGAAATCTTCC[C/G]ATATCAGAATATAGA	84628
rs370147935	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132169414	GGGTGGTTACTTCTA[C/G]ATAGATCTGGGTTCA	84628
rs370175985	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132233182	AGCCTGTGGTGGGCA[C/G]ACAGAAGCAAAAACA	84628
rs370190084	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132227703	CCCTCTCCTGTCCTC[A/G]CCCAGCCATGCCAGG	84628
rs370193074	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230398	GGGATAATCCACCCC[C/T]GTCCCCACACCCTGC	84628
rs370197173	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201394	TAAACACTCTTCAGG[C/T]GGCAGCTTGGCTTGT	84628
rs370292436	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132227955	GTCCGAGGCCCTCCT[A/G]GGCACTTTGTGCATC	84628
rs370335313	snp	C/G	4.96981e-05	0.00498463	missense	NTNG2	GRCh38.p7	9:132198102	GGAGCCGCTACCCCA[C/G]CCCGCTGGAAGCCAA	84628
rs370338856	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132200216	CTGGGGCGGGCTGAG[A/G]GAGGAGAGAGTTGAG	84628
rs370340078	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233792	GCTCCGTGAGATGGA[A/G]GCTGTTATTTTCCTA	84628
rs370404014	snp	A/G	0.000153988	0.00877328	synonymous-codon	NTNG2	GRCh38.p7	9:132226996	CGGCTCCTACCTGCC[A/G]CTGCCCCATGGCTCT	84628
rs370439562	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132194439	CCCTCACCATTCCAG[G/T]CAACAGCACAGGACA	84628
rs370471412	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132226128	CTGCAAATTCTCTCG[A/T]GAAATGCTTCTATAA	84628
rs370495685	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132236073	ACGACAGGAACCCCC[C/G]TCTCCAGCTGCCCTT	84628
rs370506631	snp	C/T	6.75733e-05	0.00581223	synonymous-codon	NTNG2	GRCh38.p7	9:132198223	GAAGTCCCTGGACAA[C/T]GGGCGCACCTGGCAG	84628
rs370508456	snp	A/G	2.32183e-05	0.00340714	intron-variant	NTNG2	GRCh38.p7	9:132227060	CGAGCCCACATGGCT[A/G]TAATCTTCCCTGCCC	84628
rs370517286	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180576	GGAACTGGGTGGCCC[C/T]GGGCAAGTCTCTTCC	84628
rs370520427	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200893	GCCCCTGGGCATCTC[C/T]GTGACCTCTGCCCTC	84628
rs370559178	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132214744	AGATGAAATACGGGA[C/T]ACCCAGTTAAACCTG	84628
rs370603959	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132185405	GGGGCCTGTCCCTCA[C/T]CCCACCCCGGCACTG	84628
rs370622269	snp	A/G	1.75188e-05	0.00295958	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240874	ACGGCGCCCACACGT[A/G]GCCCTGACCGCGCGC	84628
rs370647474	in-del	-/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132233924	CTGCTCAAGGTCTCA[-/G]AATTATGGAGAGGCA	84628
rs370662312	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219302	AGATGGCTGGGCACG[A/G]TGCTTCATGCCTATA	84628
rs370674682	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132175574	AAACGGCAGATGATG[C/T]GGGAACCGGTCTGTT	84628
rs370716413	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132217321	CACAGAAGGCAGGCA[A/G]CCTGAGGCAGGGAGG	84628
rs370732838	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132188325	CAACAGCAGTCAAGA[A/G]ACGTGCCGCCTGCCT	84628
rs370837776	snp	C/T	0.000212585	0.0103076	intron-variant	NTNG2	GRCh38.p7	9:132241837	GGTTGGCGGGGGGAC[C/T]GGGCCACCCCCCGTG	84628
rs370923345	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132211110	CCGGGGTTCACCAGA[G/T]GCCTTGGCTTGACTG	84628
rs370932091	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132205646	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	84628
rs370933580	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173810	GATGAGACGGACGGA[C/T]GGACAGACAGGCAGG	84628
rs370990712	snp	A/C/T	0.00557861	0.0525638	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230762	TCTCCACCTCTCCCC[A/C/T]CTCCACCTCCCCCCC	84628
rs371038388	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190524	CCAGTGACCGCCCCT[C/T]CACGGCCTCCTTAGT	84628
rs371052187	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195891	CCCACTTCTGCCCCC[C/T]GAGTAGCTGGGACTA	84628
rs371064796	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179710	CTCTCGTAACAGGAC[A/G]GAGCCAGGTCAGAGT	84628
rs371191307	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132232610	TGAAAGGATTTATCC[C/T]TCCCAGAGGGCACCA	84628
rs371201038	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132172130	GCTCCAGCCTTGGCC[C/T]GTGCTGTCTCCTCCA	84628
rs371287050	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223568	ACATCCTCAAAACAA[C/T]CTCTGAATGGACGAG	84628
rs371305436	snp	C/T	1.70188e-05	0.00291704	synonymous-codon	NTNG2	GRCh38.p7	9:132198391	GAAGCACGTGCGCTT[C/T]GAGGTGCGGGACCGC	84628
rs371322083	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189022	ACCACCAAAGCATAC[C/T]AGTGGATTTAATATA	84628
rs371356441	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132220510	CTGTGCTCAGGCCAG[A/G]GTGCAATCTCAGCTC	84628
rs371379264	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213137	CAACATAGTAAAACC[C/T]TCGTCTCTACTAAAA	84628
rs371454432	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132180436	GCTGTTAATCCAGAA[C/T]GCACCTTGTCTCTGC	84628
rs371475803	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217227	ACGTAGGAGCACTCA[A/G]CAAATTATTTCTATG	84628
rs371477527	snp	C/T	0.000153988	0.00877328	intron-variant	NTNG2	GRCh38.p7	9:132239064	CAGTTTCCCTGAATG[C/T]TCGCTGACCATTGGT	84628
rs371487968	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132184590	AAGCTCCGCGGGGTG[C/G]AGGGGGCATCCAAAG	84628
rs371499588	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132169462	TTATTGTGGCTTCCC[C/G]TGGGAGGGTCCGGGC	84628
rs371534022	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132238121	GTTCGGGGGCAGCCA[A/C]ATTGGCTTTCTTGCT	84628
rs371583453	in-del	-/CA			intron-variant	NTNG2	GRCh38.p7	9:132180904	GGGCTCATGCACAGG[-/CA]CACACACACACATAT	84628
rs371607754	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132192535	AGTGGAGGTTGCAGT[C/G]AGCCGAGATTGTGCC	84628
rs371657490	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132177871	CTATTTGGCCAGGCT[C/G]ATCTCGAACTCCTGG	84628
rs371734389	snp	A/G	0.000153988	0.00877328	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230606	TGGCAGTAAGTACAC[A/G]CCTGGGGAGGGTGGC	84628
rs371787820	snp	G/T	2.58481e-05	0.00359491	missense	NTNG2	GRCh38.p7	9:132226856	CTCCCCAGGTGCAAG[G/T]GCAACCTGCACGCCA	84628
rs371799440	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229247	CAGGAAACAGCCCAA[A/G]GAGACACAGAGGCTA	84628
rs371847195	multinucleotide-polymorphism	AA/GC			intron-variant	NTNG2	GRCh38.p7	9:132213261	TGGGAGGCGGAGGTT[AA/GC]AGTGAGCTGAGATCG	84628
rs372031643	snp	A/C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182885	GCTTTTCATTCCCCC[A/C/T]CTGCCGCAGCTGCCC	84628
rs372075866	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132164288	AATTAATAGATTTGC[G/T]AGTTGCGCCGCGCGC	84628
rs372112175	snp	A/C			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244953	ACGAGGCTGGGGGCC[A/C]TGGAGCGTCAATGAC	84628
rs372127069	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174057	CACACCATGCTGCGG[A/G]TGAGATGGACAGACG	84628
rs372135737	snp	A/G/T	3.56347e-05	0.00422091	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230525	GGAGGTGACACCCAG[A/G/T]CCCCTTCCCCTGGGG	84628
rs372143054	snp	C/T			intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242902	CAGAGGAATCCACAA[C/T]ACAGCCTTAAAGAAA	84628
rs372199430	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167659	ATGCAATGATGGCAG[C/T]CCCTGGGTAAGTCGG	84628
rs372209233	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174365	GCTGCAGATTAGACG[A/G]ACAGATGGACGGACG	84628
rs372218967	snp	C/T	8.75818e-05	0.00661689	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240877	GCGCCCACACGTAGC[C/T]CTGACCGCGCGCCCG	84628
rs372301655	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160024	CAAGATCTGTTCTCT[C/T]CTCCCAAGGAGCTTC	84628
rs372321370	snp	A/G	1.65359e-05	0.00287536	missense	NTNG2	GRCh38.p7	9:132239131	ACGGTCACTCCAACC[A/G]CTGCAGCTACATTGA	84628
rs372322482	snp	C/T	5.21028e-05	0.00510379	synonymous-codon	NTNG2	GRCh38.p7	9:132198289	CTTCGGTATGTCCGC[C/T]CGCCGGGCCCGCGAC	84628
rs372331146	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228508	TCTGTCCTGAGGGCC[A/G]CTCTCTCTTCCCTCC	84628
rs372352613	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132208304	TGTGGCTGTGGTGGG[C/T]GAGTAAGATTCCAAA	84628
rs372397457	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170555	TGGAGATGGGGAGGG[C/T]GTGACTGGCATTGGG	84628
rs372426296	in-del	-/GCA			intron-variant	NTNG2	GRCh38.p7	9:132165359	GCTTAAAATAGCACA[-/GCA]ATAATCGTAATTGTA	84628
rs372534851	snp	C/T			synonymous-codon, missense	NTNG2	GRCh38.p7	9:132242006	CGACCCCGCCGACGA[C/T]GACGGCGGTCTGGAC	84628
rs372550149	snp	C/T			missense	NTNG2	GRCh38.p7	9:132166964	CAGCCCAAGGTGATG[C/T]GCCTGAAGGACTACG	84628
rs372561542	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181100	GACTTTCTCTTTTTT[C/T]TGAGACAGGGTCTCA	84628
rs372683897	in-del	-/T	0.0146672	0.084371	intron-variant	NTNG2	GRCh38.p7	9:132210451	TCCAGCTCTGTCCTC[-/T]TGTCCCTTCATCAGT	84628
rs372697760	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212547	TGTCCATGTTACCCT[A/G]GAAAAGCCAGGCTGC	84628
rs372732795	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194240	GGTGCCAGAGCCCAG[A/G]TGCAAGTTCTTGGAG	84628
rs372738892	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132214156	TCCCCGCAAGGAGTG[A/G]ATGACATCACTCTTT	84628
rs372753777	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132163544	TTTCCCTCCCGGCAA[C/T]CGCCACTCTCCCCTG	84628
rs372770327	snp	A/G	6.84123e-05	0.0058482	synonymous-codon	NTNG2	GRCh38.p7	9:132198532	GCTGCTGCGCCCGGC[A/G]CTGGGCGGCACCTAT	84628
rs372778486	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132219220	ACTCTGTCTCAAAAC[-/A]AAAAAAAAAAAAGAA	84628
rs372779382	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161514	CCCCCAGAGGCTGCC[G/T]GGGCCACCCTGGCCA	84628
rs372815388	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243535	CCCTGGGGCCACACT[G/T]CCCCCTCGGTCCAGC	84628
rs372821391	snp	C/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132201480	TTCCCTCTTCAGTTC[C/G/T]GCTGGGAAAGTCCAG	84628
rs372840518	snp	G/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132237257	TCGAGGAGAGGGGCT[G/T]TGTGATTTGAGGCCA	84628
rs372878595	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168074	ACGCAGATGTTAGCC[A/G]TTGTCATTCTGGTCA	84628
rs372897815	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229540	CCCCAGGACCTCCCC[A/G]TGCCCTGCCTGATGT	84628
rs372935848	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132182260	GGAGTGGGGGAAAAA[-/A]TTGCACCCAACAATG	84628
rs372963942	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207488	TACACGCTGTCTCCC[C/T]GTGTCTCTTCCTACA	84628
rs372978069	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180982	TCCGTGGTCACTTTC[A/G]GTCAATCATCTGGCC	84628
rs373003373	snp	A/G	1.65677e-05	0.00287812	missense	NTNG2	GRCh38.p7	9:132198113	CCCAGCCCGCTGGAA[A/G]CCAACATCACCCTTT	84628
rs373054223	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132209421	GTGACGATGACGCCC[A/G]CCGTGGGGGCGTGCG	84628
rs373114901	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218744	TCAGGTGATACACCC[A/G]CCTCGGCTTCCCAAA	84628
rs373128080	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132225896	GAGTCCAGATCTTGC[A/G]GATGGCATCCCCTGG	84628
rs373129921	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217977	TGATGTGGCCGGTGT[A/G]GTCCATATCGCTCCT	84628
rs373133334	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132210674	GGGCCTCACCAGCTG[C/T]GATTGGGCAGGACAG	84628
rs373210053	snp	A/C/T			intron-variant	NTNG2	GRCh38.p7	9:132165960	CGTCTCTATTCTCCC[A/C/T]CTCTTTAATTTGTTG	84628
rs373249148	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175672	TGTTTCTAATTCCCC[A/G]AGCACACACCAACTG	84628
rs373250562	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207858	CCTGTAACCCCAGCA[C/T]TTTGGGAGGCTGAGG	84628
rs373303354	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199926	CAGCCTTTACCTCCC[A/G]AAAACTGTTTAGACT	84628
rs373333460	snp	C/T	0.000115419	0.00759581	synonymous-codon	NTNG2	GRCh38.p7	9:132166888	GGCCTCTGGGGACTA[C/T]GACATCTGCAAATCC	84628
rs373335177	in-del	-/CGGACAGA			intron-variant	NTNG2	GRCh38.p7	9:132174132	GGACAGACGGACAGA[-/CGGACAGA]TAGGCAGGCCGCACC	84628
rs373403351	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187747	TCTTACCAATAAATA[A/G]GAAGTAATCTGTTAA	84628
rs373506653	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184191	TTCATCGGCCCCACC[A/G]CCTCTTAACTCCTCA	84628
rs373523349	snp	A/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132219818	CTGCTATCAACATTC[A/T]TGTACACATTTTGTG	84628
rs373573445	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241272	GGGCCTAGTGAGAGC[C/G]GGGCAGGGTTGGGAT	84628
rs373610645	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172705	ACGCTTCTCAGAGGA[A/G]GCAGGATCAGGGCTG	84628
rs373626940	in-del	-/G/GG			intron-variant	NTNG2	GRCh38.p7	9:132215079	TTTTGTAGAGATTGG[-/G/GG]GGGGGGGGGTCTCAC	84628
rs373706194	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132228077	CCTCCCAGGTTTCAC[A/G]GTGAGTTGCATGCCA	84628
rs373748798	snp	A/G			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243774	CAGCAGGAGATTACA[A/G]CACAGAAAAGGAGGG	84628
rs373758539	snp	C/T	0.000153988	0.00877328	intron-variant	NTNG2	GRCh38.p7	9:132226817	CTGCCCACAAGCTCT[C/T]TGACATCTCTGCCCT	84628
rs373761912	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200988	GCTCAGGGCTGGGAA[C/T]CAGCTCCCCAGGCCC	84628
rs373780531	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132184015	GGGCACGAAGGATGT[C/T]CACAAATAGTTGATG	84628
rs373787886	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174003	AGGTCGAACCATGCT[A/G]CGGATGAGACGGACG	84628
rs373791646	snp	C/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132214136	CTCACCGCTTCCTCC[C/G]TCATTCCCCGCAAGG	84628
rs373795769	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188819	GTTCATTCATTCTCC[A/G]AAGATTTCCCGAGTC	84628
rs373865073	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132196706	TTTCCACACCAACAA[A/C]CTAGTCTCCAGCTCT	84628
rs373932338	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242522	GGCCTGTGCCAGGCT[C/T]ACGGGCGGCGGCGGA	84628
rs374069014	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132165886	CCAGTTTTCTCGGGA[A/G]ACTTTGCTAATGCAG	84628
rs374082042	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230685	AGAGAAAAAAGGGGC[C/T]TCAGTGTCCCCTCTG	84628
rs374138515	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190472	AGGCCAGCTGCATGA[C/T]GTTGTCTGTTCTTCT	84628
rs374149104	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132206226	AATCATCCATGGACT[C/T]CCTGAAATATATGCT	84628
rs374150084	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174341	GGACAGACAGACAGG[C/T]CGAACCATGCTGCAG	84628
rs374153171	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132222187	CCTCAGTGGAGTGAG[A/G]TAGGATCAAGGAGCA	84628
rs374209460	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188583	GAGCGTGGGAGGTGG[A/G]GTTGAGGCACACAGG	84628
rs374222976	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132220702	ACCTGCCTGCCTCAG[C/G]CTCCGAAAGTGCTCA	84628
rs374253447	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132207489	ACACGCTGTCTCCCC[A/G]TGTCTCTTCCTACAG	84628
rs374272806	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230941	TGGGTGGGCTCCCTG[A/C]TCCTCCTGCCACCCA	84628
rs374288421	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132206432	AACACTTTGGGAGGC[C/T]GAGGCAGGTCCATCA	84628
rs374320068	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132235633	CATAACTTGGTTTCT[C/T]CTCTTCTTCCCCCCA	84628
rs374368572	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174514	ACCCTGAGCCTTGGT[C/T]TTCTCATCTGAAACT	84628
rs374381449	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132175751	AGTCAGAGTGCTAGG[C/T]CCTGGCTGCTGAGAG	84628
rs374457521	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207155	CTCTGCGAGCTTTCT[C/T]GCCATCATATTAATT	84628
rs374514879	snp	C/T	0.0115493	0.0751254	intron-variant	NTNG2	GRCh38.p7	9:132241844	GGGGGGACCGGGCCA[C/T]CCCCCGTGCTGACCG	84628
rs374572684	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218051	CAAGATATTGTTTCC[C/T]GCTCTTCAGGTGAGA	84628
rs374591802	snp	C/T	3.51438e-05	0.00419174	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230532	ACACCCAGGCCCCTT[C/T]CCCTGGGGCAGCCAG	84628
rs374611012	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227689	TGCTCTCTGCCCACC[C/T]CTCTCCTGTCCTCGC	84628
rs374683238	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132182254	GGGGAAGGAGTGGGG[-/G]AAAAAATTGCACCCA	84628
rs374687311	in-del	-/GA			intron-variant	NTNG2	GRCh38.p7	9:132165341	TTTAAATAATTAACA[-/GA]AGCTTAAAATAGCAC	84628
rs374695516	snp	A/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132237090	AGGTCTTAGCAGGGC[A/G]CGGGGGTGTCAGGGG	84628
rs374698161	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132188657	CGGGGCCTGCTGTTT[A/G]CTGAAGCACCAGGCC	84628
rs374720621	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132218338	GAAGATAATAATGAC[A/T]TGTCATTCAGGGGAT	84628
rs374731181	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201523	GCCAGAGACACAGGA[C/T]TGGTGGCAAAGGGGG	84628
rs374736805	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132203710	CCGTGGTAGCAGCTG[C/G]ATTCGATGGGCCCAA	84628
rs374737860	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183293	GGGCTGTCACGGGCG[C/T]TGCTTAATGTCAAGC	84628
rs374814149	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132174560	CACAACCTCGAAGGA[C/G]GTGTGTACAAATAAG	84628
rs374939709	snp	G/T	2.32723e-05	0.0034111	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230584	CAGGTGCCACTGCAG[G/T]TTCCTTTGGCAGTAA	84628
rs374942794	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181809	AGAATTTAAGCCACT[C/T]GCCGAAGGCCACACA	84628
rs374946207	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132211931	TCATTCATTCATTCA[G/T]TCAGTCAGTCATTCA	84628
rs374953735	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232693	TCCAATAGCCTGCCA[C/T]ACCCTGTCCCCCGCC	84628
rs374962769	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187326	ACAAAACAGAAAAGC[C/T]GCCTTGGCCAGCTGC	84628
rs374971995	snp	C/T	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132215751	GGGGTGGGTGTTGGA[C/T]GGGACAGCATGAATA	84628
rs375007384	snp	C/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244562	GTTCCATGCACACTT[C/T]CCAAGTTCTTGGCCC	84628
rs375012346	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185419	ACCCCACCCCGGCAC[C/T]GAAACCCTCACAGCC	84628
rs375021739	snp	A/G	0.000162386	0.00900925	intron-variant	NTNG2	GRCh38.p7	9:132198622	CAGGTAAGGCCGGGG[A/G]AAGCCCTGGATGTCA	84628
rs375023271	snp	C/T	0.000170646	0.00923548	intron-variant	NTNG2	GRCh38.p7	9:132227065	CCACATGGCTATAAT[C/T]TTCCCTGCCCGTCAA	84628
rs375029497	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170854	CTGCCCCACAACTGC[C/T]GAGCCAGACTCTGCC	84628
rs375039285	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132168357	GTGTCCTTGGAGGAG[C/G]CTCCAGGTCTCTGGG	84628
rs375077085	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188332	AGTCAAGAGACGTGC[C/T]GCCTGCCTCCCCGTG	84628
rs375087244	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180871	AACCACGCATGTGCA[C/T]ACGTGTGTGCAAACA	84628
rs375091265	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205504	CAGCTTCAGTTTGCG[A/G]TGATTTAAAGTTCTG	84628
rs375109462	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132225950	CTCTGTCTTTCCTGT[-/T]GCGCTCACAGCTGGG	84628
rs375139056	snp	C/T			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243211	CTCGGTGGCCACCTC[C/T]GATGGATGTGTCATC	84628
rs375169333	snp	A/C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173915	GATGGACGGACGGAC[A/C/G]GACAGATGGACAGAC	84628
rs375178394	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202145	AGCGATCCCACGGGA[C/T]TCCCCTTTGAATTGA	84628
rs375183535	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217280	ACTTCATCTCCCGAG[A/G]GCCTTCCAGAATAGG	84628
rs375204040	snp	A/G	5.02803e-05	0.00501374	intron-variant	NTNG2	GRCh38.p7	9:132239067	TTTCCCTGAATGCTC[A/G]CTGACCATTGGTATT	84628
rs375322246	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174318	GCGGATGAGACGGAC[A/G]GACGGACGGACAGAC	84628
rs375337112	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132185360	GGGAGGGGATCCGAG[A/G]AGAGGCAGCTACCAA	84628
rs375435243	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224257	CCCCCTGCACAGTTT[C/G]CCCTATTTTGGAGTA	84628
rs375553791	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187249	AGCGCTTGGAGGCTC[A/G]CTTGCCTGCCCCTGC	84628
rs375604326	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212260	GGCTGCTTAGGCTGG[A/G]GGTGCCTTCGCAGGC	84628
rs375652747	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132186540	CCTGATGAGCAGTGG[A/G]TGCCCACACCAGGCC	84628
rs375675763	snp	C/T	1.71141e-05	0.00292519	synonymous-codon	NTNG2	GRCh38.p7	9:132198253	GCCCTACCAGTTCTA[C/T]GCCGAGGACTGCATG	84628
rs375720433	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185835	CAGGGAGGAGGAGGA[A/G]GAGTGGGAGGAGGAG	84628
rs375737442	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132201052	TGCTCAGGGAAACCC[A/T]CATCTTCAGGCAACT	84628
rs375746278	in-del	-/CA			intron-variant	NTNG2	GRCh38.p7	9:132233286	GCAAGTGCACACATG[-/CA]CACACACACATGCAT	84628
rs375806871	snp	G/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132194918	CTCAGCCCCTCAGAA[G/T]GCGGTGGGCCCCATT	84628
rs375828314	snp	C/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132210580	CCCCACCCAGTTCTG[C/T]CTGGGCCACTCCCTC	84628
rs375835045	snp	A/C	0.000153988	0.00877327	missense	NTNG2	GRCh38.p7	9:132198288	CCTTCGGTATGTCCG[A/C]CCGCCGGGCCCGCGA	84628
rs375839100	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132238198	AAGGGATGCCCCCCC[-/C]ATTCTTAGGGATGGT	84628
rs375864667	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229637	ACCCCGAGGTGTCCT[C/T]AGGGTCTAGCAGGTG	84628
rs375907739	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167672	AGCCCCTGGGTAAGT[C/T]GGGGGAAGGCAGACA	84628
rs376030120	snp	A/G	0.000153988	0.00877328	intron-variant	NTNG2	GRCh38.p7	9:132239290	AGAGGGCACGGACAC[A/G]GCACAGGGAACTTGC	84628
rs376182137	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193571	TTTCTGGGTAGGTGA[C/T]GCAGTGTGACGCCAC	84628
rs376196256	snp	A/G	0.000755333	0.019419	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240864	GTCCGAGAAGACGGC[A/G]CCCACACGTAGCCCT	84628
rs376237767	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132179541	CGATCGCAGCAATGC[C/T]GGCGATCATGGTGCT	84628
rs376239734	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132194432	TCTCAGTCCCTCACC[A/G]TTCCAGGCAACAGCA	84628
rs376256128	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214055	CTTTGCCTTTGCAGA[A/G]AGCCAGCCCTGGGGC	84628
rs376272278	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132209566	AGCGGCCACCTGTGT[C/T]CATGCTGCGGCGGGT	84628
rs376293213	snp	A/G	5.38643e-05	0.00518934	intron-variant	NTNG2	GRCh38.p7	9:132167078	CTTTTGTTTGCCCAG[A/G]CCAAGTGGGAGGAGG	84628
rs376294203	in-del	-/GAA			intron-variant, cds-indel, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237513	GTGATGCCTATTGAA[-/GAA]TTCCAAGGTAAGAGG	84628
rs376351222	snp	G/T	2.48747e-05	0.00352657	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230615	GTACACGCCTGGGGA[G/T]GGTGGCCAGGGCCCC	84628
rs376392921	in-del	-/AG	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132165340	TTTTAAATAATTAAC[-/AG]AAGCTTAAAATAGCA	84628
rs376413278	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132174207	GCTGCAGATTAGACG[A/G]ACAGATGGACGGACG	84628
rs376446367	in-del	-/GGACAGAT			intron-variant	NTNG2	GRCh38.p7	9:132174133	GACAGACGGACAGAT[-/GGACAGAT]AGGCAGGCCGCACCA	84628
rs376465254	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188345	GCCGCCTGCCTCCCC[A/G]TGGAACCCGAGTCTG	84628
rs376483531	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172391	TGCTGTGTGATCTCT[A/G]ATGTGAGACCTAACC	84628
rs376549523	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132228260	ACAGGCATGTCACGC[A/G]TGTGCTACAGCAGGC	84628
rs376623172	snp	A/G	3.48791e-05	0.00417592	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240892	CCTGACCGCGCGCCC[A/G]TGCCCGTGTCCGTCC	84628
rs376718098	in-del	-/CAGTCA			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228979	CCCCACCCTCACCCC[-/CAGTCA]CCACCTCCAGTCTAG	84628
rs376725654	snp	C/T	1.65611e-05	0.00287755	synonymous-codon	NTNG2	GRCh38.p7	9:132239183	CGTCAGCTGCAAGCA[C/T]AACACGCGAGGTCAG	84628
rs376730417	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132201117	CTCATGTGGGGCCCT[C/T]ATGTCTGGGCCAGCT	84628
rs376750387	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196444	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	84628
rs376805767	snp	A/G	0.0111196	0.0737302	intron-variant	NTNG2	GRCh38.p7	9:132173877	GACGGACAGACAGGC[A/G]GGCCGCACCATGCTG	84628
rs376833213	snp	A/G			missense, synonymous-codon	NTNG2	GRCh38.p7	9:132242010	CCCGCCGACGATGAC[A/G]GCGGTCTGGACTGCG	84628
rs376856895	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211356	TTGGTTTCGGGACAT[A/G]ACTGGCCTCCCTCCC	84628
rs376909053	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132186530	GGTCTGCGGTCCTGA[A/T]GAGCAGTGGGTGCCC	84628
rs376934651	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132214640	GCAAGCAAGTGAGTG[C/T]GCCCCATGTCAGGCC	84628
rs376959714	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132184425	ACACCCGTCATTAAC[C/T]GAAGAAGCCACTGGG	84628
rs377012651	snp	A/G/T	0.00021761	0.0104288	intron-variant	NTNG2	GRCh38.p7	9:132239284	TTGGTGAGAGGGCAC[A/G/T]GACACGGCACAGGGA	84628
rs377071434	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170585	GAGGTGCCCCTTAGC[A/G]CTCTGCAAGACACGT	84628
rs377099191	in-del	-/AAG			intron-variant	NTNG2	GRCh38.p7	9:132219587	CAAAAAAAAAAAAAA[-/AAG]AAAGAAAGAAAGAAA	84628
rs377117537	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132177734	GCGATCTCAGCTCAC[A/T]GCAACCTCCCCCTCC	84628
rs377161693	snp	C/T	0.000153988	0.00877328	missense	NTNG2	GRCh38.p7	9:132198123	TGGAAGCCAACATCA[C/T]CCTTTCGTGGAACAA	84628
rs377218733	snp	C/T	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132190049	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	84628
rs377240118	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205462	GGGCTGGGGGAAGGC[A/G]GAATGGGGGTTAGTA	84628
rs377242268	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219505	TTGAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC	84628
rs377245588	snp	C/T	0.000262026	0.0114431	intron-variant	NTNG2	GRCh38.p7	9:132227045	CATGCCCCGGGGCCA[C/T]GAGCCCACATGGCTA	84628
rs377252579	snp	C/T			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166576	CCAGGGTTAGGAGGA[C/T]GTGAAGTTATGGGCA	84628
rs377281000	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228890	TCCACTTGCCCCCTG[C/T]GCCTGGAGGGTTCTG	84628
rs377298016	snp	A/G	2.02272e-05	0.00318012	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240998	CGCGGCGGGCCCCAA[A/G]TGCGACGACTGCCTC	84628
rs377308810	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193709	TCCTCCCGGCCTGTT[C/T]CCTCTTTGCTCACCT	84628
rs377312703	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132208431	GTGTGATCTGATTTC[C/T]GGTGTTTGGAAATCT	84628
rs377350504	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204515	TATTCCTGTACCCAC[C/T]CTCCCTGCATCTCTT	84628
rs377354551	snp	C/T	0.000181874	0.00953437	synonymous-codon	NTNG2	GRCh38.p7	9:132226981	CCGGTCCTGGCGGGC[C/T]GGCTCCTACCTGCCG	84628
rs377354584	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132219089	GGGTGTGGTGGCACA[C/T]GCCTGTAATCCCAGC	84628
rs377376747	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132184971	GGCAGAGCTGGTGGC[A/C]GAGCCAGGCCCAGGG	84628
rs377446111	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132208519	TGACAGCAGCCTGGC[C/T]GGGTTCTGGCAGGGA	84628
rs377524726	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132243033	GCGGCCAGGCTGCAG[A/G]TGCCCCACCTGTTAG	84628
rs377544766	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220141	TTGTATGCCTTCTTC[A/G]GAGAAATGTCTGTGC	84628
rs377561867	snp	A/C/T	0.000454165	0.0150626	intron-variant	NTNG2	GRCh38.p7	9:132197951	CACCCTTCCCTTCTC[A/C/T]TCTCCCCGCTGCAGG	84628
rs377575125	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187417	TGCTGTCTGTTGTCC[A/G]GGGCCTGTGCACGAA	84628
rs377588604	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132169931	GGAAGATGCAGGCTG[G/T]GGGAGCTTCCTCGCC	84628
rs377598079	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132235786	CTTAGACTCGTAGGC[A/C]CCTCCCTCTGTAGTG	84628
rs377603051	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132225967	CGCTCACAGCTGGGT[C/G]TAGAGGCTTGATCTG	84628
rs377606122	snp	G/T	0.0283406	0.115616	intron-variant	NTNG2	GRCh38.p7	9:132216861	GGCACGTGGCAAAGG[G/T]GGCTTCTTTCTTCTT	84628
rs377723273	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132228570	CTCCTTTTTTTTTTT[-/T]CTTAAAGATAAGTCT	84628
rs386739038	in-del	AGG/GGACAGACAGA			intron-variant	NTNG2	GRCh38.p7	9:132174326	GACGGACGGACGGAC[AGG/GGACAGACAGA]CAGGTCGAACCATGC	84628
rs386739039	in-del	ACAGA/G			intron-variant	NTNG2	GRCh38.p7	9:132174332	CGGACGGACGGACAG[ACAGA/G]CAGGTCGAACCATGC	84628
rs386739040	in-del	AGCAAGACTCTGTCTC/TCTCA			intron-variant	NTNG2	GRCh38.p7	9:132174906	CAGCCTGGGCGACAG[AGCAAGACTCTGTCTC/TCTCA]AAAAAAAAAAAGTGT	84628
rs386739041	multinucleotide-polymorphism	CA/TG			intron-variant	NTNG2	GRCh38.p7	9:132175553	CCGGGCCATGAGGAA[CA/TG]GGAGAAACGGCAGAT	84628
rs386739042	multinucleotide-polymorphism	AA/TC			intron-variant	NTNG2	GRCh38.p7	9:132186008	TAGCCTCACCCGGCC[AA/TC]CCTCTCTCCTTTTTC	84628
rs386739043	multinucleotide-polymorphism	CC/TT			intron-variant	NTNG2	GRCh38.p7	9:132188952	CAGGAGAAAGATCTT[CC/TT]CCTCACCCATTCTAT	84628
rs386739044	in-del	CCTTT/G			intron-variant	NTNG2	GRCh38.p7	9:132189063	GAAAAAGGCTTTAAG[CCTTT/G]CTTTTTTTTTTTTTT	84628
rs386739045	multinucleotide-polymorphism	CCAGA/TTGGG			intron-variant	NTNG2	GRCh38.p7	9:132206590	GAGAATCACTTGAAC[CCAGA/TTGGG]AGGCGGAGGTTGCAG	84628
rs386739046	in-del	AG/GAT			intron-variant	NTNG2	GRCh38.p7	9:132215488	GGGAGGCTGAGGCAG[AG/GAT]AATTGCTTGAACCCA	84628
rs386739047	in-del	CTTGTTT/TG			intron-variant	NTNG2	GRCh38.p7	9:132225229	GCCCTTTTGTTTTGT[CTTGTTT/TG]TGTTTTTGTTTTTGT	84628
rs397686787	in-del	-/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132218496	TTTTTTGTTTTTTTT[-/T]GTTTTTCTGGTTTTT	84628
rs397722815	in-del	-/A	0.5	0	intron-variant	NTNG2	GRCh38.p7	9:132176195	TCTCAAAAAAAAAAA[-/A]GTCTTATTGTGTCTA	84628
rs397790662	in-del	-/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132228570	TCCTTTTTTTTTTTT[-/T]CTTAAAGATAAGTCT	84628
rs397841810	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132232818	CTTCCCCCTTGGGGG[-/G]TGGCATTTCTAAAGG	84628
rs397946143	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132210911	AAGTCACACACACAC[-/AC]GCAGCCATTCACTCA	84628
rs398069033	in-del	-/CCC			intron-variant	NTNG2	GRCh38.p7	9:132179004	ATGAGGCACATCCcc[-/CCC]tctcatttcctatga	84628
rs398087599	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132232817	CCTTCCCCCTTGGGG[-/G]GTGGCATTTCTAAAG	84628
rs398096704	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132189420	TGGCTTAAAAAAAAG[-/G]TATCATCTCCTGGTG	84628
rs398096705	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132214874	AAAATTCAAAAAAAA[-/A]TTTTTTTTTTTTTTA	84628
rs398113929	in-del	-/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239647	TGGTGTGTGGGGGGG[-/G]TCCCCCTCCATAGCT	84628
rs527259313	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201585	AGGGACCCCTGGGGG[C/T]TCCCAGGCTCTGGGA	84628
rs527338642	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132192124	GATGGGTGGAAACGC[A/G]CAGACCCAGAGGAGG	84628
rs527358742	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199133	GAAGGTGCACATGTC[A/G]GAGGAAGGAAGTGCA	84628
rs527361200	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229971	GCCTCGCCCACTCTC[A/G]GCTATATTTCTCCCC	84628
rs527381833	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233408	AGCCGTGGGAGGCTG[A/G]GCAGATTGTGCAAAG	84628
rs527421455	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228355	GCACAAAGAGCACTC[C/T]GGGGGCTGACAGCCC	84628
rs527488232	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209495	CTGAGATCAGAGACA[A/G]GGGGAATCTGGCAGG	84628
rs527565171	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168244	AGTGCTCCGGAGGCC[A/G]TCCCTGGCAGGGCAG	84628
rs527603895	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168651	GACCGCAGGGCCAAG[C/T]AAGGGGGCTGGGCTC	84628
rs527632599	snp	G/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132233325	CACAGGCATGCACAC[G/T]CACATGTACACACAC	84628
rs527693021	in-del	-/TTTG	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132225240	TTGTCTTGTTTTGTT[-/TTTG]TTTTTGTTTTGTTTG	84628
rs527696982	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227543	TGGGGTGTTTGGAGC[G/T]AGCCACCAAGGCCAA	84628
rs527712445	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184592	GCTCCGCGGGGTGGA[G/T]GGGGCATCCAAAGGG	84628
rs527722196	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234656	GCTGCGGGCGGAAAA[C/T]GCCGCTGGAGACACT	84628
rs527796651	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179479	GACAGAAAGAGTGCT[C/T]TGTGCCAGGAGGGCA	84628
rs527813003	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221860	TCTTGGATTCGGCCG[A/G]TCTTCTATGCATCTT	84628
rs527848736	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237004	GTTTGGAGAGGCGGT[A/G]GGGAGAGCAAGAGAC	84628
rs527861176	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203032	CTCTGGTTAGACGGT[A/G]GGAGAGGGAAGTGGG	84628
rs527897146	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196835	CCCCCACCTCTGACG[C/G]AATTGCAAGTTCCTG	84628
rs527938363	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190009	GAGGCCGAGGCGGGC[A/G]GCTCATGAGGTCAGG	84628
rs527939335	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132197434	AAAAGGCTCAGGAAG[A/G]TGACTCAGCTAAGGA	84628
rs527990686	snp	C/T	0.00124766	0.0249454	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231507	TGGCTGGGAAGCCAG[C/T]GAGCCGAGAGGGCGC	84628
rs527990709	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237608	CGGTGCAGGATAGAG[A/G]ACCGATGCCTGGCTC	84628
rs528037474	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190527	GTGACCGCCCCTCCA[C/T]GGCCTCCTTAGTCAG	84628
rs528054344	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220736	TACAGGCGTGAGCCA[C/T]CGCACCTGGCTCCCT	84628
rs528059088	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213476	TCTTGGCCATGTAAG[C/T]CCGCAGCCCCCTCCC	84628
rs528097431	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207659	TCTTTTCGGGAGACA[C/T]GATTTGGCCCACAGC	84628
rs528109204	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205097	CATGTAGATTTAGCA[A/G]TTCCGCTCCTAGGTA	84628
rs528159887	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132172886	AGGCACCTGCCACCA[C/T]GCCAGGCTAATTTTT	84628
rs528174329	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244162	TCAGTTGTCCAAGTT[C/T]GTGGCTCTGGTTTTT	84628
rs528239040	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208205	CTTTGAAGGAGAAAC[C/T]TGAAGGGGGAACGGG	84628
rs528242512	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132225249	TTTGTTTTTGTTTTT[G/T]TTTTGTTTGTTTTTG	84628
rs528324729	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132182699	CAGGAAAGGGAGGTT[C/T]CAGGTTTTGTGGCTC	84628
rs528452869	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165845	CCGATCTCCAAATGT[G/T]CAACTCTGATATTAA	84628
rs528455286	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207137	TGCCTAAGAAGGCAT[G/T]TCCTCTGCGAGCTTT	84628
rs528466520	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132201406	AGGCGGCAGCTTGGC[C/T]TGTCGTTGAACTCGG	84628
rs528572993	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188571	CAGGATCCCTGGGAG[C/T]GTGGGAGGTGGGGTT	84628
rs528669102	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240178	CAGAGGAGGGGCTCC[C/T]GCAAAGCTGGAGCTG	84628
rs528726969	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176125	AGGCCGAGGCAGGAG[A/G]ATCACTTGAGGCCAA	84628
rs528777848	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237735	GAAGCCAACTTGGGC[A/G]CAGTGGGCAGGCCAC	84628
rs528803021	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212822	TGGTCACTTGTCACC[C/T]CTTACTCAAGCTGGC	84628
rs528816579	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171434	TGTTTATCCAATCTT[G/T]ATAAGCTTGACATTT	84628
rs528824138	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206779	ACTGCATCTCCCAGG[C/T]CCCCTGAGCTACTGC	84628
rs528830443	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229323	GGCACCGACACCCAC[A/G]GGGCCAAGTGCAAGT	84628
rs528929832	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188190	GGCCCTCTACCTGGG[A/C]ACCCACACCCAGGGC	84628
rs528954913	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181347	TTTTTTTGAGACGGA[C/G]TCTTGCTCTGTCACC	84628
rs528971748	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223749	CAGGCCTCTATTCGC[A/G]GGATCTCACTGATCT	84628
rs528981802	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217680	CCTGTTTGTCTCATG[C/T]AAGAGCTTTATAGAC	84628
rs529004891	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132224312	ACTGATACAGTGTCA[C/T]TCACTAGGGCCTGTT	84628
rs529038864	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163099	TTAAGAGAGGCAGTG[C/T]CGAAAAAGGGGGCGC	84628
rs529061907	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205637	TGTAATCTCAGCACT[C/T]TGGGAGGCCGAGGCG	84628
rs529099709	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199735	AGGACAGTCCAACGG[C/T]TTATGGATTAGAGGT	84628
rs529128617	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200401	GAAAAAGTGATTTGC[C/T]GTATGGCAGGTAGAG	84628
rs529149985	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171717	AGTCCTTGAGCCACT[C/T]CTCACTGTGACATTG	84628
rs529199318	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192245	CTGGGGTGGGGGGAC[C/T]GGGGTAAACTGGTCT	84628
rs529200857	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240457	AACTGGGCCCACCCC[A/G]GGAGCAGGAATAGGC	84628
rs529236633	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186635	ATCAGGGCAGCCCAA[C/T]GCCCTCAGGTCCTCC	84628
rs529266875	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216276	ACTGTGTGCCAGGCA[G/T]TGTGTTAGACATTTA	84628
rs529272762	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210518	TAGGTATAGCCAAAG[C/G]TACTTTGGAGGAGAG	84628
rs529289583	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132188208	CCACACCCAGGGCCT[C/T]TCCTGGGCAGCCTCC	84628
rs529291670	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213099	CAGATCACCTGAGGT[C/T]GGGAGCTCAAGACCA	84628
rs529306367	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132216706	CTGGTGAGATTGATG[G/T]TTCCTGAGGGTCAAA	84628
rs529325946	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174790	AGCCGGGTGTGGTGG[C/T]GCGCGCCTGTAATCC	84628
rs529326024	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132169007	AACCCAGTGCAGTGG[A/G]CGGCTGTTCTGGGGA	84628
rs529334598	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227880	AGACTGCCCCTGGGG[C/T]GGGCTCTCCCTGACC	84628
rs529344742	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132210806	TCTCAGCAGAGGGAG[C/T]GTGGGGTGGGTCATT	84628
rs529442004	in-del	-/AAAAAA	0.343701	0.231776	intron-variant	NTNG2	GRCh38.p7	9:132178787	CTCTACTAAAAATAC[-/AAAAAA]AAAAAAAAAAAAAAT	84628
rs529498896	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132185321	GAAGAGGAGAGGGGG[C/T]CCAGAAAAGGCCCCC	84628
rs529499460	snp	G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132198788	ACCTGGTTCCCCGGG[G/T]GTTACCTGGTATGTG	84628
rs529506057	in-del	-/CA	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132198693	GATACCTGGGATGTT[-/CA]ACCTGGTATGTGGAA	84628
rs529509775	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132191415	CACAGACCATCTCAC[A/G]TGGCAATCAATAAGA	84628
rs529549618	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191877	CGCCCGGCCATTACC[A/G]CATCTTTCTAGAGAA	84628
rs529549979	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132237204	GCTTGGGATGTGCTG[G/T]GTTTCCTTCAGGAAG	84628
rs529565457	snp	A/C	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132186009	AGCCTCACCCGGCCT[A/C]CCTCTCTCCTTTTTC	84628
rs529580468	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132228310	GGGGTGACTTGGCAG[A/G]CACCCGACAGCACTC	84628
rs529599794	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244466	ATTACAGGCATGAGC[C/T]ACCGCACCACCTGCC	84628
rs529601053	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132180247	CAGAAGTCTGCTGTC[A/G]GGCAAAAGGTGAAGA	84628
rs529633875	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132203884	AGGAAGGCAGCCCAG[C/T]GGGTCCTTTGCCAGC	84628
rs529647409	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168166	ACTCCAGGAGGTGGC[A/G]AAGCTGTGATTCCAG	84628
rs529670008	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209410	TGAGCTCCGCGGTGA[C/T]GATGACGCCCGCCGT	84628
rs529755045	snp	A/G	1.65471e-05	0.00287633	missense	NTNG2	GRCh38.p7	9:132239109	GCCGGCCCAGACTGC[A/G]AATGCTACGGTCACT	84628
rs529766429	snp	C/T	3.39202e-05	0.00411812	synonymous-codon	NTNG2	GRCh38.p7	9:132198421	CTTCGCCATCTTTGC[C/T]GGCCCCGACCTGCGC	84628
rs529790322	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160626	CAGGGAAGGGTTAAG[A/G]TGGAGGTGAAGGGTG	84628
rs529840450	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214783	ATAAACAAGGGAATC[A/G]TTGTTTTTTAGGGTA	84628
rs529935142	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200254	GGTGCTGGGGCAGTC[C/T]GGGCCAGGAGCCTGG	84628
rs529981256	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208897	ACCCCTGGAAGCCCC[C/T]ATCCTGCTCCCTGAA	84628
rs529994100	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173642	GGGCAGGCAGTGGAT[A/G]GATGGACAGACGAAC	84628
rs530030942	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173865	GATGGATGGACAGAC[A/G]GACAGACAGGCAGGC	84628
rs530036647	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196818	TCAGTCGCACCACAC[C/T]GCCCCCACCTCTGAC	84628
rs530049821	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132237050	TGTGATGTCAATCTA[G/T]CTAAAAACAGTTTGG	84628
rs530102290	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183917	ATTTCTGACCTTAGG[A/G]CCCAGGAATGTTGCC	84628
rs530122287	in-del	-/C	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132214230	GGGAGACTCTCCAAA[-/C]CCCCCCGCTCCTCTC	84628
rs530125844	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132172798	GCAGCGGCGCAATCT[C/T]GGCTCGCTGCAAGCT	84628
rs530129770	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226589	TGAGATGTGAGGAAT[C/T]CTTGAAACCAGCATC	84628
rs530164834	snp	C/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132220848	ACTTCATTCTTTTTA[C/T]GTGGGTCTCCCATAT	84628
rs530173479	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190452	CCAGCGCAGGCTTGG[A/G]TGCAAGGCCAGCTGC	84628
rs530190447	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166620	TCCATCAGCAGTCTG[A/G]GAAACGCTGGCTCTG	84628
rs530203090	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231931	AGAGACGCTAGAACC[A/C]TAGAGCTGGGAGGCC	84628
rs530211523	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184468	CCAGTGCTCCCTTGG[A/G]ACTGGGGGGCAGTGG	84628
rs530245099	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202260	CAATGTAGGCAGGAG[C/G]GGGAGGACAGAGGCA	84628
rs530279769	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192821	GTGTTGGCCGCGGCT[C/T]GGGATTTATTTATTG	84628
rs530305974	in-del	-/TGG			intron-variant	NTNG2	GRCh38.p7	9:132220066	ATCTCATTATGGCTT[-/TGG]TGTGCATTTCCCTGA	84628
rs530395917	snp	A/C	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132236318	GGGTCCTGGAAGACA[A/C]TGACATCCTCCTGCT	84628
rs530408603	snp	A/G	4.95143e-05	0.00497541	synonymous-codon	NTNG2	GRCh38.p7	9:132166849	GCTGCATCTGCTGGC[A/G]CTCTTCCTGCACTGC	84628
rs530433361	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236944	AAGGGAGATGCCAAA[A/G]TCCTTAAATGCCAAG	84628
rs530438674	in-del	-/C	0.0189856	0.0955633	intron-variant	NTNG2	GRCh38.p7	9:132238191	GAACATCAAGGGATG[-/C]CCCCCCCATTCTTAG	84628
rs530461294	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176650	TGATACTGCTGTGGA[C/T]ATTTGGGTCTCAGTT	84628
rs530472889	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240343	CACCCTCCTCCTCTC[C/T]CTGGCTCTCCCTGCC	84628
rs530497389	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171556	GGGCAGGCTGTGAAC[A/G]TGCATCTTTGAACAC	84628
rs530498978	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132177030	AGTCTCATTCTGTCA[C/T]CTGGGCTGGAGTGCA	84628
rs530522907	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132219847	TGTGGACATGTTTTC[A/G]TTTCTCTTGGTTATA	84628
rs530529761	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212993	TCTTGACTCAGGCCT[C/G]GGCATAGCAGATGGG	84628
rs530559669	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213431	TCCATCCATTGGCCA[C/T]GGCCACCCACCGGCT	84628
rs530560043	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132207286	ACTAACTGGGTGGAG[C/G]TCAGGAGTCTGAAAT	84628
rs530567269	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132182903	GCCGCAGCTGCCCCC[C/T]AGACCAGCTTCAGCA	84628
rs530574011	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235747	AAGGCCTGTGATGGG[C/G]CTGAGACCCCGGGGA	84628
rs530615463	in-del	-/CCA	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132216268	AGCACCTACTGTGTG[-/CCA]CCAGGCAGTGTGTTA	84628
rs530681106	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188803	AGTAACCTCATTGAG[C/T]GTTCATTCATTCTCC	84628
rs530711555	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132186254	TCTGGTCCATTCTGT[A/C]AGTCGCCTGTGGGGT	84628
rs530722155	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201679	CTCCGCTGTGGCCCA[A/C]TAACAAGAACAGCAA	84628
rs530723978	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194790	GAACCGAGGGTCAGC[C/T]CTGCCACCGAGGAGC	84628
rs530747331	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187949	GGGGAAACCAAGGCA[C/T]AGATAGGGCAAGGCC	84628
rs530754746	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160902	AGGCTGGCAGGAAAC[C/T]TCCTGGGGATCAGAG	84628
rs530758948	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188335	CAAGAGACGTGCCGC[A/C]TGCCTCCCCGTGGAA	84628
rs530761334	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132195339	TTTGAGACAAAGTCT[C/T]GCTCTGTCGCCCAGG	84628
rs530763838	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170813	AGCGCTGACCTCACC[C/T]TGATAGAGGTGCAGA	84628
rs530819092	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224426	CATAAAGAATGGTTT[C/T]ACCGCCCTAAAAATC	84628
rs530832543	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206640	CCATTGCACTCCAGC[C/T]TGGGTGACAGAGCAA	84628
rs530847211	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240812	AGCATCCCCTGGGGA[A/G]TGTGGAGATGCTCCC	84628
rs530896866	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164855	AGCCCTGGGGCCCTG[A/G]CTGGGGGCTGCTCCG	84628
rs530952333	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200598	GAGGCTGGGCAGGCC[A/G]CTGTGGTGCTGCTGT	84628
rs530955338	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180032	CCCTGTGGAAAGGGA[C/T]TCAGGCCTGTCTTCA	84628
rs530989095	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201330	CTCTGCGGGCGGCGG[A/G]GAGGAGCCGAGGTGG	84628
rs531018789	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217562	TATACTCTGCATAAG[G/T]TTCCTGTGAAGAGGT	84628
rs531024158	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167286	GGGTAGGGGCATTCT[C/T]GGCCAGCTGGCCACT	84628
rs531061007	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170180	CAGATGCGGGGTGCA[A/G]ACCCTCTCTCTTTCC	84628
rs531172216	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181169	GCTCACTGCAGCCTC[C/G]ACCTCCTGGGCTCCA	84628
rs531198622	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192239	TGGGGACTGGGGTGG[A/G]GGGACTGGGGTAAAC	84628
rs531212011	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175512	CCCTGTGGCCAGCAC[G/T]GATGCAGGGCTCCTT	84628
rs531248479	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170419	GGCGGCCCCCACCCA[C/T]ATTCCCAGGGCCTGC	84628
rs531284563	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132211700	AGCTCCTGAAGGCTG[A/G]AGACCTGTGCAACCA	84628
rs531292808	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233904	TCAGAAGAAAAAAGG[A/G]GCAGCTGCTCAAGGT	84628
rs531311589	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187304	GGAAAATTGCTCCAA[C/T]CAGAAAACAAAACAG	84628
rs531334055	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223224	GGCAGCCCTGGTTAC[C/T]AAAGCTGGCAGATGG	84628
rs531401075	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132186774	CCACCGCCTCTCCCC[C/T]AGGCAGCGTCCTACC	84628
rs531408147	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193898	GGCTTGGAGCCAGCC[A/G]CCTTCTCACTGTGCC	84628
rs531424682	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205180	GTTTATAGCAGCTTT[A/C]TTCAGAGTAGTCAAA	84628
rs531435453	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180763	GACCCAGAGGGGAGA[A/C]ATGCAGGGAACCTAC	84628
rs531468992	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132209929	GGAGGGCGGGAGGGA[C/T]GCTGGGGACAGGAGC	84628
rs531497136	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169566	ACATCACTCCGTTGA[A/G]AAGGCAGGCTGGGAA	84628
rs531526376	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233425	CAGATTGTGCAAAGT[G/T]GGGAATTAAAGAGGA	84628
rs531619656	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215855	TACTCTCATCTCCGT[C/T]CCTCCCTCTATCACC	84628
rs531627134	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132161898	GCGCGGGTCCTCCCC[G/T]GGCCGCCCAGGGGGG	84628
rs531638597	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179544	TCGCAGCAATGCCGG[C/T]GATCATGGTGCTGGG	84628
rs531643960	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239841	CAGCTCTTTTTTGTG[A/G]CTGAAGCTTTTCTTC	84628
rs531691999	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173971	AGATGGATGGACAGA[C/T]GAACAGACAGGCAGG	84628
rs531726114	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168358	TGTCCTTGGAGGAGC[A/C]TCCAGGTCTCTGGGT	84628
rs531745794	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222559	TGGCTAGTGCTGCTG[G/T]CCAGGGCTCTTGCTC	84628
rs531848493	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174276	GATGGATGGACAGAC[A/G]GACAGACAGGCAGGC	84628
rs531886648	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185171	ACCACTGCTGGGGAC[C/G]AGGCTTCACTCTCAG	84628
rs531891523	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132238438	AGCGAGTCAGAAGCC[A/G]GGCCAGGACCAGGGG	84628
rs531916397	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177712	ACCCAGGCTGGAGTG[C/T]AGTGGTGCGATCTCA	84628
rs531963964	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132167118	GATCCTTGGGGTGGA[C/T]GAGCAGAGCTGGAGG	84628
rs531966081	snp	A/G	0.000123571	0.00785941	missense	NTNG2	GRCh38.p7	9:132198278	TGCATGGAGGCCTTC[A/G]GTATGTCCGCCCGCC	84628
rs531987679	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192935	CTTCCCGGGCCGGGG[C/T]GGGGGCCGGAGTGCC	84628
rs531989911	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223581	AATCTCTGAATGGAC[A/G]AGAGCCAGTCAGGGG	84628
rs532071083	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244733	CCTCTGTCCAGAACA[G/T]GACTGCCCCTGCCTT	84628
rs532078189	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132227650	ATGTGTCCTCTACGG[C/T]CTGCACCAGAGTCCC	84628
rs532088568	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229377	CCCTCCTCCCGCCAC[G/T]TTCTTTGAACTTCCC	84628
rs532115759	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132214668	GCCGTGAGAGAAGTC[A/G]GGGTCTGAGCAGAGG	84628
rs532127278	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237789	AAATAGCCCATCCCG[A/G]CTCCCCTGGGAGGTG	84628
rs532130921	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208338	GAGCAGGCAGGGCCA[C/G]ATCACGCCAGCCCTG	84628
rs532145928	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226477	CAGCAGCCTCTGTCA[C/G]CCATCAACCCACATC	84628
rs532167688	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132203066	GGCTTGGGGTCAGGG[C/T]TGCCTAGATATGAGG	84628
rs532179493	snp	A/C	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132173609	AATGACAAGCTGCCT[A/C]CAATCCCACCTGCGA	84628
rs532202898	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132203742	GCAGGGCCAACACAC[C/T]GGAGCCAGGGCAGGG	84628
rs532219271	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167824	TCTGAGTGTGTGGGC[C/T]GAGCCTGATGCCATT	84628
rs532341162	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166020	TCTCCTCCCCTCTTA[A/C]AATGAAAGACAAGTC	84628
rs532362193	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236216	AGCACATTCCAGGCC[A/G]CAGGGCCAGCCGGGG	84628
rs532366684	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202163	CCCTTTGAATTGAAG[A/G]TTCTTTGATGGGTGG	84628
rs532433041	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195985	TGTGTTGCCTGGGCC[G/T]ATCTCAAACTCCTGG	84628
rs532467860	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230885	TCCATCAGTGCTGCT[C/T]TGGAAAACGGGACAG	84628
rs532501591	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226007	CAGTTGCTTTGGCTT[C/T]GGGTGGGGGTGTGTT	84628
rs532540459	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232207	TGGTCCCTGGAGCCC[C/T]GCCCACACCCTGTCC	84628
rs532587482	snp	A/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132207181	TAATTCACTCAACAG[A/T]TGTTTTTTCTCAGAC	84628
rs532625554	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132201809	CCAATGGTTATTGAA[G/T]GGCTCAGATCCCACA	84628
rs532625620	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132207521	GACACCAATCACATC[A/G]GATAAGGGCCCGCCC	84628
rs532644577	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132189750	GTTCAAATGATTCTC[A/G]TGCCTCAGCCTCCTG	84628
rs532657840	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183134	CTCTCACATCTGAGC[C/T]GCAGGTGCTCCATCC	84628
rs532662089	in-del	-/TTTT	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132196161	GTACAGGTCTATGGG[-/TTTT]TTTGTTTGTTTTGTT	84628
rs532699472	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243399	AAGATTAGGAAGGGG[G/T]GCTGGAGGGGACAGG	84628
rs532760326	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188257	CGGCAGCAGCCTCCC[A/G]TCCTGGTGAGGCTGA	84628
rs532779539	in-del	-/GCTGACAGGACAGAGG	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132209972	CGGGGTGGGCGGAGA[-/GCTGACAGGACAGAGG]GCCCACCAGCATGTG	84628
rs532796362	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181933	CTGGATCTCAGAAAG[C/T]GCCTGATAGACGGAG	84628
rs532839799	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165939	CGGAGAGCTTTTGTT[C/T]TTATACGTCTCTATT	84628
rs532859637	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235869	ACCAACTGAGGGCAC[A/G]GGTGTAGAATGTCGG	84628
rs532880822	snp	A/G	0.00199481	0.0315187	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166540	GATTTGATCAGATTC[A/G]CCTCCAGGGGAGGTG	84628
rs532931058	snp	G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132224361	TCTGTGTTGGACACT[G/T]CAGTGGGTTTTGCCA	84628
rs532932804	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218885	CTGGAAGCTGTAAGC[C/T]CTTCCCTGTTTCCAC	84628
rs532949035	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132241528	GGGGACAGAGGGAGG[A/G]AGGCTGTCCAAGTCG	84628
rs532966188	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168583	AGGGAAGGAGAAGGC[A/G]GCACGAAGCCAGGAG	84628
rs532970279	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225023	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	84628
rs533024807	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132187458	AAAGGGAAGGAGAGA[A/G]ACACCTGCACGCTGG	84628
rs533054954	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177965	CCTGGCCTCAAATCT[A/G]TTCCTCTGAAGCATC	84628
rs533074586	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235139	AGAAGGGCAGTGATC[A/G]GGGAAGCAGGTCAGA	84628
rs533165689	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132183446	GCCCTTTGCTCAGTC[A/G]ACCTAGAGCACCATC	84628
rs533171047	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201696	AACAAGAACAGCAAA[C/T]GTTTATCGAGCATTT	84628
rs533203236	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169848	GCTTTGCTTCTTCCC[C/T]GGGCTCCTTTGCCTC	84628
rs533237720	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227843	GCCAGGAAGCCCCTG[A/G]GCTGCAAGTGGAGAA	84628
rs533239354	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163206	GAAAAGCAGCTGCGG[A/G]GCTGCCGGGTCGTCG	84628
rs533254631	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170249	AATTGTAAATTCCAG[C/G]CTTGCAAGGAAGGGG	84628
rs533256341	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234863	AGCTGGAAAGTCTTC[C/T]GCACTTGTTAGCTGG	84628
rs533274450	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164084	TCCCCCTTCTCTTTT[A/T]TCTTTTTGGCAGAAC	84628
rs533301423	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229840	TGTGGCACCAGCTCC[C/T]TCCTTTTGCAACTCT	84628
rs533312379	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132211140	GCCCTGGGCTCAGGG[C/T]TTCTCTGTGCTTCTC	84628
rs533321200	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228755	CAGAGAAAAGGTTTT[G/T]CCATGTTGCCCAGGC	84628
rs533338610	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222664	TACATGTAACCTAAA[A/G]CGGTGGGTTCCTGAG	84628
rs533348153	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211154	GCTTCTCTGTGCTTC[A/T]CCCCCATGTTGAGGC	84628
rs533358170	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192815	AAAATTGTGTTGGCC[A/G]CGGCTCGGGATTTAT	84628
rs533385587	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132211621	CATGACCTAGCCCTC[C/T]CCAGCCTTCCTGTCT	84628
rs533394652	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180287	TGAGAGATGAGCCCA[C/T]GGTGCTCCTGCCCTC	84628
rs533449968	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132196283	GCAACCTACGCCTCC[A/G]GGGTTCAAGTGATTC	84628
rs533470243	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240658	TGACCCAGGCCACAC[C/T]AGTGCCAGGGCGGGG	84628
rs533506299	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233005	TTCCTTTTCTGCAGG[A/G]GGCATTTACAGGAGG	84628
rs533600095	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132186744	TCCCCAAAGCGGAGC[A/G]AAGCCCGCGGATGCC	84628
rs533619262	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179240	ACAGGATGCCTGCCC[A/G]GATGCCACCTGCAGC	84628
rs533631473	snp	A/C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174292	GACAGACAGGCAGGC[A/C/T]GCACCATGCTGCGGA	84628
rs533635914	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180642	GGGGGTCTGCAGGTC[A/C]ACCTCAGAGTCCCAC	84628
rs533640402	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227785	GAGGACCACCCACCC[A/G]GGCGCGCTAGCGTAG	84628
rs533645000	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132221633	GCGAGTTGAAGAGGC[C/T]GGGACATCTTCTCCT	84628
rs533684945	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132174795	GGTGTGGTGGCGCGC[A/G]CCTGTAATCCCAGCT	84628
rs533721581	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208985	CTCACTGTGCCTCTG[A/C]GGCTTATGGCGTGGC	84628
rs533727158	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216732	TCAAATTCAGAGAGC[A/G/T]ATCGCTTGGGAAAAT	84628
rs533781708	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132226221	GATAAATGCTTGATT[A/C]TTTCCCTTTATTTAC	84628
rs533790923	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132197109	TAAAAAGGCTCAGGG[G/T]CCGGGCGCAGTGGCT	84628
rs533793067	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237400	TGACAGACGAAAGAA[A/C]CTGTTTCTCATCTCT	84628
rs533801698	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184855	TGAACCCGGGAGGCC[A/G]AGGTTGCAGTGAGCC	84628
rs533856805	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132232263	TCCTTAGCCCCTCAG[C/T]AGCACACCGGTGGGA	84628
rs533925351	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132222068	TGCGAATTAAAACCT[C/T]CCCAGGTCAGATTTT	84628
rs533928555	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132224799	AAGATGGTGTCTGCC[A/G]TGATGAACCTCTGTG	84628
rs533929901	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184052	TGAATGAATAAATCA[A/G]TGAAACTTACCAGCC	84628
rs533937209	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132177279	GGCGTGAGCCACCAC[A/G]CCCAGCCTATTTTAA	84628
rs533939964	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214231	GGGAGACTCTCCAAA[A/C]CCCCCGCTCCTCTCT	84628
rs533981941	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132179181	CTCTGTCCATCTACA[C/T]GTGCCCTGGATCTGA	84628
rs534021793	snp	A/G/T	0.000399281	0.0141238	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244932	TGGCCAGCCCTGGCC[A/G/T]GATCCACGAGGCTGG	84628
rs534044884	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230950	TCCCTGCTCCTCCTG[C/T]CACCCACGCCACTTC	84628
rs534065599	in-del	-/AAGT	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132214631	CAGCTTCCAGCAAGC[-/AAGT]GAGTGCGCCCCATGT	84628
rs534065657	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160056	TCCTGCATAGAACAG[A/G]TAACCAGGGGTGGGC	84628
rs534072868	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208458	ATCTGAGTTGGGGGT[A/G]GCGGTGCTGGAGGCC	84628
rs534079047	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237884	TGGGACACTTAGAGG[A/G]TGCCTCATCTCCTCA	84628
rs534094544	snp	G/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132219071	TAAAAAGACACTCTG[G/T]CCGGGTGTGGTGGCA	84628
rs534169050	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228860	ACCACGTCTGGCCAT[A/G]TCTGGCTTTTTTCTT	84628
rs534260321	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220169	TGCTGATCCTTTCCT[C/T]ATTTTAAAAACTGGA	84628
rs534298213	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167298	TCTCGGCCAGCTGGC[C/T]ACTAGTTCAGTTCCC	84628
rs534326807	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201902	GGGGCAGCGCTCCCC[C/T]AGCCTCGTGTTTTCA	84628
rs534349932	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243058	TGTTAGGAGCCTCCC[C/G]ACACTGAAAGGCTGC	84628
rs534360721	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165963	CTCTATTCTCCCCCT[C/G]TTTAATTTGTTGCAG	84628
rs534383018	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196254	GGAGTGCAATGGCAC[A/G]ATCTCGGCTCACTGC	84628
rs534429721	snp	C/T	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132232039	TTCCAAAGTCGTCTT[C/T]CTCCTGCCCTTCAAG	84628
rs534455260	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195574	CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	84628
rs534542911	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132226720	GGTTGGGCTGGTGGC[C/T]TCCAGGGTTTCTTCC	84628
rs534573507	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171150	GGAAGGTTCCAGAGA[C/G]AGGCAGCACTACCTC	84628
rs534615394	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165536	TTTCAGATTGTGCCT[A/G]TGATTGGGGGGCTGT	84628
rs534662669	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235273	TTCGCAGCCATTAGC[C/T]AGAGACATCAGCTCA	84628
rs534731354	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132236499	GGTGAGCTGTTCCTT[C/T]CAGCTCACATGTTCA	84628
rs534759754	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202449	GAAGCACAGGCACCC[G/T]CAAGTCCCAGCCACG	84628
rs534792067	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229975	CGCCCACTCTCGGCT[A/C]TATTTCTCCCCAAGC	84628
rs534820657	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212584	CGACCAACCCAGACC[A/G]CCCAGACCTCCCCTC	84628
rs534841793	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224523	CTGCTAGACCCGAAG[A/C]ACCATCAGGTCAGGG	84628
rs534875021	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184926	AAACTCTGTCTCAAA[A/G]AAAACAAGGCTGGAA	84628
rs534891504	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176736	CTGGGTCACAAGGTA[A/G]TTCTATGTGTAACTT	84628
rs534909418	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132219081	CTCTGGCCGGGTGTG[G/T]TGGCACACGCCTGTA	84628
rs534914369	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240259	GATCAAAGCCGCTGA[C/T]GTCACAGGGGGCCAG	84628
rs534978840	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229589	GCCTCACTTGGTCAC[C/T]ACCCAGTCCTGGCCC	84628
rs534991401	snp	C/G	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132164387	TGCAAGCCCCGAGCA[C/G]CCGCGGGTCCTGCAG	84628
rs535008515	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234828	TTAAAGTCAATTCAT[C/G]TCCAAAGCTCCCCGC	84628
rs535074627	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181595	GTCGGGATTACAGGC[A/G]TGAGCCACCGTGCCT	84628
rs535168843	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217002	TCCCCATGGAATGGA[C/G]GCGAAGCCAGCACTG	84628
rs535200572	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211323	CCCTAGAAGAGAGGT[A/G]CAGGCTGGCGTCAGG	84628
rs535226758	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200146	CCTGGCACATAATAC[A/G]CACTAAAAAAAAGTG	84628
rs535249876	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187018	TGCGGGGTGAGGGGC[A/G]GTGAGGAGAGCCGCT	84628
rs535254825	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132191611	CTCTGTCGCCCAGGC[C/T]GGAGTGCTGGAGTGC	84628
rs535398609	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229005	TCCAGTCTAGCCAGC[C/G]ATGGATAGACAGGCC	84628
rs535502563	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168396	GGGGCTGACCCGGTG[C/G]CCCCACCTCAGAGTC	84628
rs535517028	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132174997	CAGAAGAGGACCCCA[C/T]AGGCCAAACCCACAG	84628
rs535551956	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169985	ACCAGCCACCAGGGG[A/G]CGCCCTAATGGCGGC	84628
rs535593595	snp	A/C/T	8.73972e-05	0.00660998	synonymous-codon	NTNG2	GRCh38.p7	9:132198604	CAACATCGAGGTCAT[A/C/T]GGCAGGTAAGGCCGG	84628
rs535593644	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162179	GGGGAGGCGCAGCGC[A/C]GGAGGGTGGCGGTCC	84628
rs535626935	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205840	GAACTGAGATCGCAC[C/T]ACTGCACTCCAGCCT	84628
rs535716611	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132228453	TCTCTCTTTAGTGGC[C/T]GTCACTCTCTCCCTG	84628
rs535754141	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168056	CTGGCACAGAGTAAG[A/T]GCACGCAGATGTTAG	84628
rs535756859	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222857	ACACCTATAATCCCA[A/G]CACTTTGGGAGGCTG	84628
rs535803841	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209058	CCGTGTGCACTGCAC[A/G]CCGTGGTCTGTTTAC	84628
rs535808612	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209770	CAAGCTTTTGAAAAC[A/G]TTTTGCTCGGAAGGG	84628
rs535812076	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132202141	ATGGAGCGATCCCAC[A/G]GGACTCCCCTTTGAA	84628
rs535913280	in-del	-/AG	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132163791	CTAATTCAATAAGAC[-/AG]AGAAATCTGAGTTCA	84628
rs535920616	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132235301	TCAGAGAGGTCTGGG[C/T]CCAGAGGCGGGACCT	84628
rs535926247	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132184182	CTTTACTCTTTCATC[A/G]GCCCCACCGCCTCTT	84628
rs535926304	snp	C/T	0.0001358	0.00823904	synonymous-codon	NTNG2	GRCh38.p7	9:132198502	GTTCTTCACCCTCAC[C/T]GACCTGCGCATGCGG	84628
rs535954014	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132239393	ACTGTGGGAATTCTA[A/C]CTCCAGGGCCCTCTC	84628
rs535958942	snp	G/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240705	GTGTTTGATCCCAAG[G/T]AAGGAAGCCAGAGTC	84628
rs535982466	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132212192	CCTGGTCCTTCCCTC[A/G]GGGGTGTTGGGCCTT	84628
rs536005189	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221616	GTTCTGGGGCTCAGC[C/T]AGCGAGTTGAAGAGG	84628
rs536059617	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202680	AGCGGGAGGGGCCTC[C/T]GCCCCCACCCTCCAC	84628
rs536080830	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179182	TCTGTCCATCTACAC[A/G]TGCCCTGGATCTGAC	84628
rs536091557	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243739	GCTAAGACCAAGTGG[A/G]ACAAACTTGGCCTTG	84628
rs536098296	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166720	CTGGGACACCCCGGC[C/T]ACCCTCGCCTGGTAG	84628
rs536105720	snp	G/T	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132236615	TAGAGAGGGTCTGAG[G/T]CTCGGTTCCTAGAAA	84628
rs536126129	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132182894	TCCCCCCCTGCCGCA[A/G]CTGCCCCCCAGACCA	84628
rs536143654	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221992	CACAGCCCCGGTTCC[A/G]TACAGCTGAGGTGTT	84628
rs536147935	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215083	TGTAGAGATTGGGGG[C/G]GGGGGTCTCACTTTC	84628
rs536174301	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132233791	AGCTCCGTGAGATGG[A/C]GGCTGTTATTTTCCT	84628
rs536196002	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219326	GCCTATAATCCCAGC[A/G]CTTTGGGAGGCCCAA	84628
rs536263147	snp	C/T	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132223940	TCATTGCAGACCTCA[C/T]GGGTGGAACTTCTTT	84628
rs536276629	snp	A/C	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132190193	ACCCGAGATAGCGCC[A/C]CTGCACTCCAGACTG	84628
rs536322715	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232208	GGTCCCTGGAGCCCC[A/G]CCCACACCCTGTCCC	84628
rs536380991	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226650	CAGGTGTGGCCTTTG[A/G]AACACGGCGTTGATC	84628
rs536423959	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195054	GGGCCACAAGTGGTC[C/T]GGAGCACTGGGTGGT	84628
rs536423977	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201870	CCTGATCCCCACCCC[A/C]TGGAGCGCTCCCCGC	84628
rs536490665	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173062	AAAAACTGGGGTTTG[C/G]GTCAGGACAGAGGAG	84628
rs536521966	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230402	TAATCCACCCCCGTC[C/T]CCACACCCTGCAGGT	84628
rs536608980	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132212516	TTGCGTTCCAGGAGG[C/T]GCAGCAGCCAGCATT	84628
rs536645222	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132206864	AAGTGCCGGTGTTGG[A/G]AAGGGGCCAGACTAT	84628
rs536675864	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183175	TTCCTGGGTGCCGAG[C/G]GGTGCCAGCTCTCCA	84628
rs536708435	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177231	GCCTCAAACGATCTG[C/T]CCGCCTGGGCCTCCC	84628
rs536747216	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132172270	GGCCTTCTCTGACTC[C/T]TTTGCCCAGTGGGGT	84628
rs536788474	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201495	CGCTGGGAAAGTCCA[A/G]CCATGCTGAGAAGCC	84628
rs536808909	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167552	CATGGGGAGGTTTGA[C/T]GGAGGCTCAGAGGGG	84628
rs536864990	in-del	-/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132165957	ATACGTCTCTATTCT[-/C]CCCCTCTTTAATTTG	84628
rs536874321	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188512	ATGACCCTGCGACAT[G/T]GCTCAGCCTCTCTGA	84628
rs536888058	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235961	TCTGCCCCCAAGCTC[A/T]CCTGCTTCAAGAGGT	84628
rs536911289	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175625	CGATTTGTTTTTCAT[C/T]AGCAGCAGATTTGCT	84628
rs536924173	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132164400	CAGCCGCGGGTCCTG[A/C]AGCTGAAGGAAGGTT	84628
rs536968696	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231120	AGGGCTCTGCTCGTC[C/T]AGGTCAGCTCAGGTC	84628
rs536979957	in-del	-/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132204185	GTTCCAAGAGGCTGA[-/G]CTGGGCCTGGACGGG	84628
rs537096946	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211843	CTCCAAGGGAGCAGG[A/G]ATGGGGTCTGGCTTG	84628
rs537101229	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193980	CCAAACTTCTTCTTC[G/T]TCCAAGGCCACCAGT	84628
rs537103958	snp	A/G	0.000798403	0.0199641	missense, stop-gained	NTNG2	GRCh38.p7	9:132242103	CTGGCCGCCCGCCTG[A/G]GCCGCTGAGCCCCGC	84628
rs537165316	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242977	ATTCCAGCAGGCAGT[A/G]CCCCCTCCCCGCAGG	84628
rs537165996	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229518	CCTCCAGGGCCCAAC[C/T]TGGAGCCCCCAGGAC	84628
rs537189415	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207248	ACTGCCTTGGTTTCT[G/T]GGAGCCTCCATAACT	84628
rs537199852	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132223972	AGCCCTAGGGCTTTC[C/T]TCATGCTCTTGCCTC	84628
rs537312962	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239640	TCTGGGGCTGGTGTG[G/T]GGGGGGGTCCCCCTC	84628
rs537325296	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169927	ATGTGGAAGATGCAG[A/G]CTGGGGGAGCTTCCT	84628
rs537336209	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217880	TCAGTCACCCAGAAA[C/G]ACAAAAGGAAGGCAC	84628
rs537357819	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132163545	TTCCCTCCCGGCAAC[C/T]GCCACTCTCCCCTGA	84628
rs537403603	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132228409	GCTTCCTGTCCCCAT[C/T]TCTTTGTGGTCCAAA	84628
rs537403622	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222253	CCAAAAAGGTTTAAG[C/T]ACAGAAACTTTCTGT	84628
rs537411957	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171346	CCTGGGAGAGGAAAC[A/G]CCTCTCACAACATAA	84628
rs537465730	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193358	CCCAATAAGCACATT[A/C]ACAACTCTATGATGG	84628
rs537494272	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234153	CCTGCCTCAGCCTCC[C/G/T]GAGTAGCTGGGATTA	84628
rs537504328	snp	A/G	0.0130921	0.0798413	intron-variant	NTNG2	GRCh38.p7	9:132187173	CCCTGGGGGAGGAGC[A/G]GGGGCGGTCGCCGTG	84628
rs537532851	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216160	GCCGTGACACTCACC[A/G]GCCTTTAACCCAGCA	84628
rs537532907	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229141	AGCCCCAGGAAGGAG[A/G]GGTTTCTTCTGGCAT	84628
rs537600345	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191103	ACCTGCCTCCTGTGG[A/G]TTGCTGAGAGGGTGC	84628
rs537616346	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132210661	TCTGTGGCTTGCTGG[A/G]CCTCACCAGCTGCGA	84628
rs537616868	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132188764	CTGGCATCATTCCTA[A/T]GACAACCCTGTGAAG	84628
rs537635928	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197899	CAGGGGCTAGGCCGC[A/G]CAGAGGCTTCCCAGG	84628
rs537637735	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204511	ACCCTATTCCTGTAC[C/G/T]CACCCTCCCTGCATC	84628
rs537672860	snp	C/T	1.70953e-05	0.00292359	synonymous-codon	NTNG2	GRCh38.p7	9:132198541	CCCGGCGCTGGGCGG[C/T]ACCTATGTGCAGCGG	84628
rs537693239	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169207	CATGGGCAAGTCCTC[A/G]GCGTCTCGCCACCTG	84628
rs537778964	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132199267	GTGAATGGGCTCTCA[C/T]GTTCAGGGGTTTCCG	84628
rs537801861	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132228328	CCCGACAGCACTCTC[A/G]GGTCTTCAAAGGCAC	84628
rs537824338	snp	G/T	0.00914312	0.0669923	intron-variant	NTNG2	GRCh38.p7	9:132208558	GTGATGTGGGCCGCC[G/T]GGAGGTGGTCTTTGG	84628
rs537837840	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132185413	TCCCTCACCCCACCC[C/T]GGCACTGAAACCCTC	84628
rs537865770	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179853	ACACAGGAGTTCGAA[C/T]GGTCGTTCTGAAATT	84628
rs537891609	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132167379	TCCTGTGTAGGAAGT[C/T]AGCATTCTGGGCGAG	84628
rs537893696	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132200085	CTCTTGCTGGATTGT[G/T]GTGAGGGTTAAATGA	84628
rs537939552	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174524	TTGGTTTTCTCATCT[A/G]AAACTGGGCATGGCG	84628
rs537990349	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160810	CTGCAGTGAGCCCAC[A/C]CCAGGAGGCCAGGAG	84628
rs537998796	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132204132	CCCCTTTCTGCCCAG[A/G]AGCAGGCTGAAGTCC	84628
rs538060816	in-del	-/TA	0.424193	0.179323	intron-variant	NTNG2	GRCh38.p7	9:132216427	CTCTGTGTGTGTGTG[-/TA]TGTGTGTGTGTGTGT	84628
rs538076250	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132184126	CATCCACAGAGGGGT[C/G]TACCTGTCCAGGTGT	84628
rs538085645	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132238726	GCACAGCCAGGTGGC[A/G]TGACCCTGCCCTCCT	84628
rs538095731	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132191593	CTTTTAGACAGAGTC[C/T]TGCTCTGTCGCCCAG	84628
rs538124336	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233079	GACCCAGGAATCCTC[C/T]TTGGGGTGGAAGACA	84628
rs538154441	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132178997	ACTACTGATGAGGCA[C/T]ATCCCCCCCTCTCAT	84628
rs538190851	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132214443	CAGCTGGGCCTGCCA[C/T]GTTTCCCAGAGAACT	84628
rs538205964	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237616	GATAGAGGACCGATG[C/T]CTGGCTCCGAAAACC	84628
rs538278185	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196335	AACTGGGATTACAGG[C/T]ATGCACCACCACGCC	84628
rs538313445	snp	A/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168016	TGTGGTTTAATTAAC[A/G/T]TAGGTAAAGTGTTCG	84628
rs538328549	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216802	CAGCAGGAGCCCAGA[C/T]TGCCCGCCCAGGTCC	84628
rs538335438	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231216	GCGAGGGCGACATGG[C/T]GCCCACAGGTTATCA	84628
rs538350337	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225923	CTGGTGTCGTTCAGG[A/G]TGATGCTCTGTCCTC	84628
rs538367224	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207976	AGGCATGGTGGTGTG[C/T]GCCTGTGGTCTCAGA	84628
rs538395854	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226785	GAGGCGCTCCTTTCC[C/G]CAGAGGCCAGGCCAG	84628
rs538425072	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132190101	AGCTGGGCGTGGTGG[C/T]GGGCACCTGTAATCC	84628
rs538462932	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132203204	TGGAAGCCAGGCATG[G/T]TGGTGTGCGCCTGTA	84628
rs538501142	snp	A/G			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244915	GCAGGGCCCAGCCCC[A/G]GTGGCCAGCCCTGGC	84628
rs538521303	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132215551	AACCACTGCACTCCG[A/G]TCTAGATGACAAAGC	84628
rs538522470	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132166165	GCAGAACCAAATAGC[C/T]TTCTCCCCAGTGAAC	84628
rs538566007	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243629	GCCACTGCTCCACCT[A/G]CAGGTGCTCCCAGCA	84628
rs538573317	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132221568	CTGCTAGACAGGGCA[A/G]TTCTCTCCTTTGGAA	84628
rs538603867	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230317	CGGCTCTGAGATTCA[A/G]TGTCTCCTTCTGCAA	84628
rs538607655	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132224629	TATTTTTCTTTGCAT[A/G]TTTTAATAAAAATAG	84628
rs538686167	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132196888	GGCTGTAAATTGGGG[A/G]TTCCCACGACCCCTC	84628
rs538708393	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237032	GACGGGCGTGGTGTG[A/C]AATGTGATGTCAATC	84628
rs538744540	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231620	CCCCCCAACCCTCTC[A/T]TGCTTTTCCCATCTC	84628
rs538755401	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226232	GATTCTTTCCCTTTA[C/T]TTACCAGTTTTCAGA	84628
rs538790505	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219109	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	84628
rs538839010	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213514	CATCATTCCTCACTG[C/T]AGTCCAGGTCCCCAA	84628
rs538848148	snp	C/G	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132207387	CTCCTGGTGGGGCCG[C/G]CAGCCTCTGGCGTTC	84628
rs538945108	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235402	GCAGATTCTCAGGCA[A/T]GGGTTCACCTCTCAT	84628
rs538959171	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132171170	AGCACTACCTCCTGA[C/T]AAGAGCTACAGGCCT	84628
rs538996743	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132222682	GTGGGTTCCTGAGTG[A/C]CCCCTCTCCCACGGC	84628
rs539019813	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211397	CTTGCCCTTTCTGTA[A/G]TTTTTTGTCCCTAAA	84628
rs539025357	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188462	AGTGGGCCATCCCCT[A/G]GCTTCTTATCCCACC	84628
rs539032838	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217808	TTTCCTGAGGTCACA[C/T]AGTCGTTGGCAGAAC	84628
rs539058420	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132211789	AGCTACCATAGCTAT[A/G]CACGTACACGTCTGA	84628
rs539064075	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182152	TAATTCACTTATTTC[A/G]TGTCTATTTGGCAGC	84628
rs539091677	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176377	GCCCCTGAAAACCAC[A/G]CGTCTACTTTTTGTC	84628
rs539138603	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170625	GCCACCTGTGGTCCC[C/T]GTGAGAGGAAGGGGG	84628
rs539195883	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206536	TCCAGGCGTGGTGGC[A/G]TGCACCTGTAATCCC	84628
rs539206666	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132200690	AGGCAAAGGCAGGTC[A/G]TTCATGAAGCTGGAG	84628
rs539212575	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230348	AATGGGCCAATAGTG[C/G]TTCCTCCCTCCCAGG	84628
rs539242574	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132194480	TGCCCAGAGTCACCC[A/G]GCCAGTGAGTGAGGA	84628
rs539255836	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132211585	TCGGGCTGGCCTAGG[A/G]GCTAGTCCTTCTGCC	84628
rs539264557	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234910	TTCCCCACAGCCACC[A/G]TTGTGTATAATCCCT	84628
rs539278843	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187054	CAACCAAGGAACTGA[C/G]ATGCATTTTCTGGGT	84628
rs539419908	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132181495	CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA	84628
rs539533140	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179623	GGCACACGTGCTTCC[A/G]TAGTGCCATGCACCG	84628
rs539533235	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205656	GAGGCCGAGGCGGGC[A/G]GATCACTTGAGGTCA	84628
rs539542893	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240127	CCCTTGGGACACCAT[C/T]ACCCATCCCCCACCC	84628
rs539554980	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132164529	GGAAGAATTAATTAG[A/G]AACGTGCTGTGCTCT	84628
rs539605916	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231242	TATCAGTAAATGTCA[C/T]CGAGACTGTCCCCAG	84628
rs539653706	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176644	TAGGAGTGATACTGC[C/T]GTGGACATTTGGGTC	84628
rs539715290	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174342	GACAGACAGACAGGT[C/T]GAACCATGCTGCAGA	84628
rs539716301	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132168500	CAGGCTTGTCAGTGG[C/T]GATGAGGCTGTCACT	84628
rs539724755	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132175143	TGATTCGAGGGGAAA[A/G]TGTGTGGGTGACAGA	84628
rs539757596	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217064	TCCAGCTCTAGTGCC[A/G]TGCAGCCCCGAGTGC	84628
rs539776393	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223868	CTAACCAGTCAAAGG[C/T]TTGCAGAGTAAAATC	84628
rs539832514	in-del	-/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132182797	CACCAGGAGCGGAGC[-/G]GGCAGGGACCAGGCT	84628
rs539838284	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177815	GGCACTAGCCAGCAC[A/G]CCCAGCTAATTTTTG	84628
rs539861413	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191332	TCCCTGAGTTAATAC[A/G]AAGCTGCTGTTTCAA	84628
rs539876202	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192428	AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT	84628
rs539922911	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233559	TGCACCCTCAGCCCT[A/G]TATCAAGAAGCAGGA	84628
rs539942595	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167799	AGCAGAGATGGTTGC[A/G]TGCGAGCTGTCTGAG	84628
rs539993047	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216051	CACCGACTGATTCCC[A/C]AAGGCTGGTCACCTT	84628
rs540010354	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132169108	CTAGAAGAGTGCTCT[A/C]TCCCATCCCCATCCC	84628
rs540046546	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209945	GCTGGGGACAGGAGC[C/T]GAGGAAGTGATCGGG	84628
rs540058164	snp	C/T	0.0123036	0.0774623	intron-variant	NTNG2	GRCh38.p7	9:132174017	TACGGATGAGACGGA[C/T]GGATGGACGGACAGG	84628
rs540119524	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231802	CAGGTGGGTGCCAGG[A/G]TACAGCGACCCCTGT	84628
rs540156186	snp	C/T	0.000143983	0.00848357	synonymous-codon	NTNG2	GRCh38.p7	9:132226888	CCTGTGCTCCATGCG[C/T]GAGGGCAGCCTGCAG	84628
rs540175306	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191659	TCACTGCAAGCTCCA[C/T]CTCCTGGGTTCACGC	84628
rs540177565	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220737	ACAGGCGTGAGCCAC[C/T]GCACCTGGCTCCCTA	84628
rs540226193	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184308	CTAAGACCTGGTTCT[A/G]AGTATGGAACACCTG	84628
rs540238929	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207777	TCAACAAACCCAGTA[A/C]CCCCAAGTGCCCACA	84628
rs540252101	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132178534	TGAAATTGACTGCGC[C/T]CAGGAAAGGGGACCC	84628
rs540299637	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132204214	GGCAGATCTGAGCTC[C/T]AGACTGGCCAAGCCC	84628
rs540311051	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243334	CAGGTGGGCAGAGGC[A/G]GGCAGTGCAGAGACC	84628
rs540329848	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214588	GCTGAAAAGGTGGCT[A/G]TGGCTCTGTCCTTGC	84628
rs540337130	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236784	GCCTGCTCACCCACA[G/T]ATAGGGCGTTGGGGT	84628
rs540365637	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208661	TTGAGACACTGGGTG[A/G]ATGGAAATTTTGCCT	84628
rs540386637	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132226406	CTGAAGCCAGGTGCC[A/T]TTCTACACAATGAAG	84628
rs540488577	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132190222	TGGGCGAAAGAGAGA[A/G]ACTCCATCTCAAAAA	84628
rs540519751	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212884	CTTCTCTGGCTGCTG[C/T]CCATCTCCCCACACT	84628
rs540605895	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194647	CTACCCTGGCCCGGG[C/T]CTCAGTCCCCCCATC	84628
rs540667354	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166432	ATTGGAAGGACAAAA[A/G]TTAAAAGCAATCTGA	84628
rs540676790	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243839	TGTCCCGAGCCCACA[C/T]ACCAGCCCCTCCTGG	84628
rs540694504	in-del	-/TG	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132173053	TCTTGAAGGAAAAAC[-/TG]GGGTTTGGGTCAGGA	84628
rs540704298	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166766	GCTGAGGCCGCGAGT[A/C]CCGCCTGACCCCGTC	84628
rs540765649	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202717	ATTAAGAGAAGCGGG[G/T]CCCAAACCTGACCCA	84628
rs540770999	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132188645	GCTCCCTAACGGCGG[A/G]GCCTGCTGTTTGCTG	84628
rs540792792	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224954	TTGAGATGTAGTCTC[A/G]CTCTGTCTCCCAGGC	84628
rs540819595	snp	C/T	0.000175	0.00935249	missense	NTNG2	GRCh38.p7	9:132226926	GCGAGCACAACACCA[C/T]CGGCCCCGACTGCGG	84628
rs540825903	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132170172	GGCCTTTTCAGATGC[A/G]GGGTGCAGACCCTCT	84628
rs540841364	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132182862	GTGCACACTGGACTT[A/G]CCTGGGAGCTTTTCA	84628
rs540864642	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170746	CTGCCCAGGCAGCAG[A/G]GTGCCAAGGGAATCC	84628
rs540864747	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132164054	TCCTCGTTATCCGGG[A/G]ACTCCTGCCTCTCTT	84628
rs540876707	snp	A/G	0.0364509	0.129988	intron-variant	NTNG2	GRCh38.p7	9:132206594	ATCACTTGAACCCAG[A/G]AGGCGGAGGTTGCAG	84628
rs540899831	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132164726	TTTAAACAGCCAGAG[A/G]TGAGACGGGGAAAAT	84628
rs540921053	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132219434	AAAAATTAGCTAGAT[A/G]TGGTGGTGGGTGCCT	84628
rs540921695	snp	A/G	0.00438332	0.0466095	intron-variant, missense	NTNG2	GRCh38.p7	9:132241475	CTGGTGGGAACTACG[A/G]GAAAGACCGAGCTGG	84628
rs541003031	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201571	CCTGAGTGGGCACCA[A/G]GGACCCCTGGGGGTT	84628
rs541028040	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223566	ACACATCCTCAAAAC[A/T]ATCTCTGAATGGACG	84628
rs541073747	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229810	GTCCTTTCTCGGGAA[C/T]ACCGTGGGGAAAGCT	84628
rs541112851	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230114	GGACGCACTCCACCC[A/G]CGGCAGCCGCTCCCA	84628
rs541216347	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175773	TGCTGAGAGAGCGAG[A/G]ATACGCCCCCAGCCT	84628
rs541234425	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199416	AGGTGCACAGGGCTG[G/T]GTCCAGGAGATACCA	84628
rs541236654	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239613	TCAGTGGCAGAGGCC[A/C]CTGAGCATCTGTCTG	84628
rs541273844	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233686	CCAGAGCCCCCATTA[A/G]TGAAAACGATCATTG	84628
rs541274578	snp	C/T	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132195382	GGCGCGATCTCGGCT[C/T]ACTGCAAGCTCCTCC	84628
rs541334778	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242201	GCCGGGCGGTGAGAA[A/G]GGTGCGGCCCGAGGT	84628
rs541382983	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229185	GGTGAGGCTGGAGGC[A/G]CTGCTGTCCTCAGCA	84628
rs541396212	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210302	GACTTGCCCGCTCAA[A/G]TCCCAGTACTCAGGA	84628
rs541414925	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208876	TCCAAGAACTCCCGT[C/T]CCGAGACCCCTGGAA	84628
rs541418486	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132187182	AGGAGCAGGGGCGGT[C/T]GCCGTGGCTTTGGGA	84628
rs541454421	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229884	CAGGGATTTCAAGGC[C/T]CCTGGTCACACCAGG	84628
rs541489312	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201481	TCCCTCTTCAGTTCC[A/G]CTGGGAAAGTCCAGC	84628
rs541516736	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132210773	TTCTGCCCCTGGGCT[A/G]GGCTGCCTCCCTCCA	84628
rs541535617	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239676	CTCCTTTCCAGAAAG[A/G]TGGAGGAGCAGCCTA	84628
rs541536638	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132217372	GGGGGAGCTGTGGGG[C/T]GGCTGCAGTTCCAGG	84628
rs541567162	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162774	GGGAGCCTGTGAGTT[G/T]CACAGAGAAACTCCC	84628
rs541571606	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211572	AAGGCTGGGTCTCTC[A/G]GGCTGGCCTAGGGGC	84628
rs541591333	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205459	CAGGGGCTGGGGGAA[G/T]GCGGAATGGGGGTTA	84628
rs541679464	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185645	CGGTGCCTTTCCCCC[G/T]CCCGCCCCCTTATCT	84628
rs541695986	snp	C/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132181881	CCGGCCCGGCATCCA[C/G]GTTCCTAAACAGGCT	84628
rs541756429	snp	C/G	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132222418	GGGATGAGAATGCCA[C/G]GGAAAGAGTGAACAG	84628
rs541789583	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197399	ATCTCAATAAAAAAA[C/G/T]AAAATTAAAATTAAA	84628
rs541790576	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186664	CCGAAAGGATCTCAG[C/G]GTGTTCTGTGGGGGC	84628
rs541791368	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132209477	GCCGGGCGGGCTGCA[A/G]CCCTGAGATCAGAGA	84628
rs541824087	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132204229	CAGACTGGCCAAGCC[C/T]GGCTCCTGCAGACCC	84628
rs541878408	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161420	GCCCGGCTGCGCCTG[A/T]CCGGAGCCGGCTGAG	84628
rs541884660	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168632	TGGCCATAACTGCCC[C/T]GGGGACCGCAGGGCC	84628
rs541907835	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231992	TCAACCTGTTCCTGA[A/G]CCCAGCCAGGGGATT	84628
rs541965559	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191195	GTTACAATCATCACA[A/C]TCTTCTGAGTCAGCC	84628
rs542004100	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184472	TGCTCCCTTGGGACT[A/G/T]GGGGGCAGTGGCCAG	84628
rs542075284	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161576	CCCCTCCCCGGGCCG[C/T]GGCGCGTCCCCCGAG	84628
rs542089911	snp	A/G	1.64996e-05	0.0028722	missense	NTNG2	GRCh38.p7	9:132166863	CGCTCTTCCTGCACT[A/G]CCTCCCTCTGGCCTC	84628
rs542134484	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132177721	GGAGTGCAGTGGTGC[C/G]ATCTCAGCTCACTGC	84628
rs542151753	snp	A/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132202956	AGTAATGACTTCAGC[A/T]GCCTGTTGTGAGGAG	84628
rs542214898	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206324	ATGATCCCAAAATAT[C/T]TGGAGAGTCCCTGGA	84628
rs542243707	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182955	GGAGGAGGCATTAAA[C/T]CTCCCCAGGTGGTCC	84628
rs542330020	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232600	GCCAGGGGTCTGAAA[G/T]GATTTATCCTTCCCA	84628
rs542397199	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132214548	CTTACTAGGGACTCA[C/T]CCATTCAAGAAAAAG	84628
rs542479874	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167625	TGCAGCTTGGGTCCC[C/T]TTCCACTTCCATTCC	84628
rs542541294	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132203511	ATTCCAGATCTTCTG[A/C]GGTTACAAAGGAAGG	84628
rs542544449	snp	C/T	0.000146678	0.00856256	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230605	TTGGCAGTAAGTACA[C/T]GCCTGGGGAGGGTGG	84628
rs542550287	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237597	CTGGAAAAAGACGGT[A/G]CAGGATAGAGGACCG	84628
rs542580072	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225869	GTGGGTCATTACTGC[C/T]GGAGTTTCCTCGAGT	84628
rs542610098	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212799	GATCCTCAAATCCGT[A/G]TGTCCCCTGGTCACT	84628
rs542722679	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220707	CCTGCCTCAGCCTCC[A/G]AAAGTGCTCAGATTA	84628
rs542725713	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185630	TAGCCCTCTTCCTCT[C/T]GGTGCCTTTCCCCCG	84628
rs542748720	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207078	GTCACGCACAGCAAC[A/G]CCTTCCCAGCAGCAC	84628
rs542759455	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221193	CTAGAATCTGACACC[A/G]CCTCTAAATATTAGC	84628
rs542759762	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213848	GTCTCAGTATACACG[A/G]CATGTAATAATGTGG	84628
rs542810604	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132195362	CGCCCAGGCTGGAGC[A/G]CAGTGGCGCGATCTC	84628
rs542836304	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208973	GTCTCCTTCGTTCTC[A/G]CTGTGCCTCTGAGGC	84628
rs542838758	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132188148	CCTTGCCTTCCCCCA[C/T]GATTGCTTCCCCCGT	84628
rs542847439	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195776	TAGGACCACAGGTGT[C/G]CACCACTATGCCCAG	84628
rs542901485	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132192624	AAACAAGAATAGAAG[A/G]AAAGTGAGAGGAAGC	84628
rs542909711	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231243	ATCAGTAAATGTCAT[C/T]GAGACTGTCCCCAGA	84628
rs542927700	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218600	CTGTTGGGTTCAAGC[A/G]ATCCTCCTGCCTCAG	84628
rs543017537	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132200894	CCCCTGGGCATCTCC[A/G]TGACCTCTGCCCTCG	84628
rs543039467	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170821	CCTCACCTTGATAGA[G/T]GTGCAGAATCCCAGA	84628
rs543072599	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132217986	CGGTGTGGTCCATAT[C/T]GCTCCTCAGGGCCAG	84628
rs543114681	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235051	GTCCCGTTAGTCTAC[A/G]GGCTGAGCGTTGTGT	84628
rs543116369	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166368	GAGGGTTGTTTTGCC[A/G]TTGTGTTGAGCACGT	84628
rs543136905	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132207430	CTGCGTCACTCCAGT[C/T]TCTGCCTTGTCTTGC	84628
rs543152159	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194584	TGATGATAACAGCAG[A/T]CTCCTCCTCAGAGGT	84628
rs543152616	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229781	GCCACACATCCCACT[A/G]CCAATCCCACAGCGT	84628
rs543165175	snp	C/T			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243062	AGGAGCCTCCCCACA[C/T]TGAAAGGCTGCCTCC	84628
rs543171622	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201704	CAGCAAACGTTTATC[A/G]AGCATTTGCTACGGG	84628
rs543211635	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132174684	CCCAGCTCTGTGAGA[C/G]GCTGAGGTGGGCGGA	84628
rs543241678	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232912	ACAGGGGCAAATGCT[A/G]AGAGAAAGACCTCCT	84628
rs543268395	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132182208	GGGGAAGGCGAGATG[A/G]CTTTGCCTGGAGGAA	84628
rs543315158	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243207	GTGTCTCGGTGGCCA[C/T]CTCCGATGGATGTGT	84628
rs543324115	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212291	CCTGGTCATACCCAC[C/T]GTGTCACCCCTAAGC	84628
rs543347703	in-del	-/TC	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132231632	CTCTTGCTTTTCCCA[-/TC]TCTCACCAGGCATCA	84628
rs543356120	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163946	TCTTAATAATATCAG[A/G]TGAAGATAAATTTTC	84628
rs543413760	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132231619	ACCCCCCAACCCTCT[C/T]TTGCTTTTCCCATCT	84628
rs543428715	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240424	ATTCACCCTCTCCCA[C/T]AGAGCCCCAAGGCAA	84628
rs543430968	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132234544	AGTGCCTCCCAACAG[C/G]TGCTTCGGGCTCTTT	84628
rs543434166	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180156	CTGCCCAAGTCATTC[A/G]TCCACTTGACTCCAA	84628
rs543439709	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192465	GCGTGGTGGCGCACG[A/C]CTGTAGTCCCAGCTA	84628
rs543468075	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229317	GTAAGTGGCACCGAC[A/C]CCCACGGGGCCAAGT	84628
rs543476020	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186607	AGTTGACCCTCTCCC[A/G]GGCAGCTCGTCCATC	84628
rs543492688	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241239	TCGCGAGACGGGGCA[C/G]GGCCGGGGCAGTGGG	84628
rs543553547	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236934	TTCAGAAAGGAAGGG[A/G]GATGCCAAAGTCCTT	84628
rs543556516	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206219	GGGTTTCAATCATCC[A/G]TGGACTCCCTGAAAT	84628
rs543599014	snp	A/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132217186	GTTTTCACGAGGATT[A/T]GTTTAATAATGCATG	84628
rs543630373	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234427	CACACAGGCCATGGC[A/G]AGAACTTGCTTCCCA	84628
rs543670171	snp	A/G/T			intron-variant	NTNG2	GRCh38.p7	9:132204382	CCTATTGATCGCCCC[A/G/T]TAACTGGAGATGGAC	84628
rs543673217	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162921	GGGGGGAGCAGAGGC[A/G]GCGGGAAGGCGGGAA	84628
rs543693803	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132205608	TAAGGTGGCTGGGCG[C/T]GGTGGCTCATGCCTG	84628
rs543701060	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161115	AGCAGGGCCCATCAG[C/G]GTGGAGGCGGCGATG	84628
rs543761638	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233607	GCTCCAATGTGACAG[C/T]CAGTGGCCCCTACAG	84628
rs543786832	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132185963	TGTTTGAGGATCACT[A/G]AGCTCCTGGTGTGGG	84628
rs543853746	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173639	ATGGGGCAGGCAGTG[A/G]ATGGATGGACAGACG	84628
rs543875855	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222574	GCCAGGGCTCTTGCT[C/T]TGCCTCAGAATTCTG	84628
rs543954578	snp	C/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160917	CTCCTGGGGATCAGA[C/G]AGCCCAGGGCTGCCG	84628
rs544031988	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132198769	TGGTATGTGATACAT[C/T]GTTACCTGGTTCCCC	84628
rs544059978	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233284	GTGCAAGTGCACACA[C/T]GCACACACACACATG	84628
rs544076266	in-del	-/TTTGTTTTTG	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132196179	TTTTGTTTGTTTTGT[-/TTTGTTTTTG]TTTGTTTTTGTTTTT	84628
rs544115329	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188025	AATTCCATGGCCCCA[C/T]GGGTCAGGGCACCTA	84628
rs544128189	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132184947	AAGGCTGGAAAGACA[A/G]GGGAGAGAGGCAGAG	84628
rs544144394	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191867	TGAGCCACCGCGCCC[A/G]GCCATTACCGCATCT	84628
rs544146507	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132215473	TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG	84628
rs544210813	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132203471	AATGGAGACAGCAGG[C/T]GCCTCACAAGACAGT	84628
rs544263288	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168146	AGGCATCTGGCCAAG[A/G]TCACACTCCAGGAGG	84628
rs544283859	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209383	GCAGGCGAGACTGGG[C/T]GCGGGGAGTCCTGAG	84628
rs544321126	snp	C/G	0.00676609	0.0577691	intron-variant	NTNG2	GRCh38.p7	9:132165872	TTAATAAAAATAACC[C/G]AGTTTTCTCGGGAGA	84628
rs544350157	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132197246	ACACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAT	84628
rs544388844	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176981	CTTAGTCATTTTTTT[C/G]TTTTTGTTTTTGTTG	84628
rs544393755	in-del	-/TCTT			intron-variant	NTNG2	GRCh38.p7	9:132195104	TTTTTTCTTTCTTTC[-/TCTT]TCTTTCTTTCTTTCA	84628
rs544431154	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213408	ACCAACCTTGAGGCC[A/G]TCCATCGTCCATCCA	84628
rs544504866	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171882	GCCCCAGCCTCCCTC[C/T]TCTCGCCGTCACAAC	84628
rs544504873	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222984	CCAGGCATGGTGGCA[C/T]GCGACTGTGGTCCCA	84628
rs544530972	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132207970	TTAGCCAGGCATGGT[A/G]GTGTGCGCCTGTGGT	84628
rs544545753	snp	A/C	0.00119737	0.0244387	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166569	TGTGATACCAGGGTT[A/C]GGAGGACGTGAAGTT	84628
rs544602014	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243938	CTCCTGCAGCTGGCC[C/T]ATCTCTACCCTCACA	84628
rs544606293	in-del	-/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132195291	GTTTTGGGGGATTTC[-/T]TCTTTTTTTTGTTTT	84628
rs544649826	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164820	TCGCCCTAACTCAGA[A/T]GAATGAGTCCCATGC	84628
rs544654072	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188756	TGGTGCACCTGGCAT[A/C]ATTCCTATGACAACC	84628
rs544658702	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237464	CCCTGCCAAGGGCTA[C/T]AAACTTTTCCAGCTC	84628
rs544697353	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231868	GCCTCTCTTGGGGTG[A/G]GAGGGTCGGCAGCCC	84628
rs544766640	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212451	ATAGAAAAGGGCTTC[A/G]CACAGAAGCCCAAAT	84628
rs544770459	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220284	AATTTTTCTCCCATT[C/T]TGTGGGTTGTCTTTT	84628
rs544774557	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187471	GAGACACCTGCACGC[C/T]GGGGAAGGAATTAGC	84628
rs544819605	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192236	GACTGGGGACTGGGG[C/T]GGGGGGACTGGGGTA	84628
rs544836911	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132186004	GGCTTAGCCTCACCC[A/G]GCCTCCCTCTCTCCT	84628
rs544837605	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132210163	ACATCACGGTGCCAG[C/T]GAGCAGCCTGCCTGA	84628
rs544843256	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165756	AAAGTCTCTGACCCC[C/G]AAGCCGGGGCACTTC	84628
rs544880565	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213762	GGCAAGAGAAATTGG[A/G]AAACATTGCTGGCTG	84628
rs544900362	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132225691	TATCTCATAAATATA[C/T]GTTCCATTTGTTTGC	84628
rs544921468	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242289	CCCTCCCCCCGCAGC[A/T]GGGGCGCCTTGGGAC	84628
rs544933690	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132189647	TCAGCTTAAAAAAAA[-/T]TTTTTTTTTTGAGAC	84628
rs544999375	snp	A/T	0.00991701	0.0697148	intron-variant	NTNG2	GRCh38.p7	9:132238980	TAGGGCACCTTCCGG[A/T]ACCTTTTCCAAAGAT	84628
rs545066168	snp	C/G	7.12073e-05	0.00596646	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230526	GAGGTGACACCCAGG[C/G]CCCTTCCCCTGGGGC	84628
rs545072442	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160102	TGGGCTGCTTGGTGA[A/G]ATAGGCCCATCTCCA	84628
rs545135158	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170800	GCCTCAGTGCAGCAG[C/T]GCTGACCTCACCTTG	84628
rs545151305	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132195160	TAAAGCAGTTTTAGA[A/T]TTACAGAAAATTGAG	84628
rs545196176	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206984	CACTGCTGGGTGGGG[C/T]GGAGAGGGCAGGAGG	84628
rs545198007	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132201300	CCCTGGAGGTGGTTC[C/T]GCTTGGCACCCAGCC	84628
rs545236802	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201667	GTTGCCCAGTGGCTC[C/T]GCTGTGGCCCACTAA	84628
rs545275441	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223687	AACACAAAAAGATGC[C/T]GCACACCCCAGGCGG	84628
rs545279376	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229667	GGCTGCCCAGACATG[A/G]AGGTGGAGGAAGGAG	84628
rs545293242	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236050	GTCTGGTAGAGGCCC[C/T]GCCTCCCACGACAGG	84628
rs545325342	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230135	GCCGCTCCCATGGCT[C/T]CTCAGTGAGTTTTCC	84628
rs545365785	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205520	TGATTTAAAGTTCTG[A/G/T]AGAGGGATGGTAACG	84628
rs545373091	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175365	CAAGAGGGGCAGGAG[A/G]GCAATTGAGGGGCAA	84628
rs545384432	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191863	GGCGTGAGCCACCGC[A/G]CCCGGCCATTACCGC	84628
rs545405605	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205993	TGTCCAGGTGCAAAT[C/T]CTGGATTAGGTGTGA	84628
rs545412793	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181744	CACAGAAGTCTTAAG[A/G]TAGAGCTTGTATTTA	84628
rs545433024	snp	C/T	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132170050	CCATGGGTCCTTGCT[C/T]CCCTTCGCCCCTTCA	84628
rs545516472	snp	A/G	5.38092e-05	0.00518669	missense	NTNG2	GRCh38.p7	9:132226977	GCACCCGGTCCTGGC[A/G]GGCCGGCTCCTACCT	84628
rs545520090	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132212640	CCTCGCTTTCTCAGG[A/G]TCTCAGGTTTGAATG	84628
rs545537074	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240358	CCTGGCTCTCCCTGC[C/T]TCCACCCCGAGAGCC	84628
rs545554253	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206622	CAGTGAGCCGAGATC[A/G]TGCCATTGCACTCCA	84628
rs545581445	snp	A/G			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243356	GCAGAGACCCCAGAC[A/G]TGCCGGCCCTGTCCT	84628
rs545626902	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132200210	AGAGGGCTGGGGCGG[A/G]CTGAGGGAGGAGAGA	84628
rs545631985	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132187237	CCCTGGGGAGGCAGC[A/G]CTTGGAGGCTCGCTT	84628
rs545668676	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181149	AGTGCAGTGAAGCAG[C/T]CTTGGCTCACTGCAG	84628
rs545690522	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132210457	CTCTGTCCTCTGTCC[C/T]TTCATCAGTCAACAG	84628
rs545699953	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217536	TGTCTGTGAAATAGA[A/G]ATAGTCATAGTATAC	84628
rs545729447	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210893	TCCCTTAGATGTACC[C/T]GCCAAGTCACACACA	84628
rs545745648	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174642	CTCAAAAAAAGGGCC[A/G]GGTGCACGGTGGCTC	84628
rs545765645	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171907	CACAACCCTCCAGTC[A/G]GCAGATGTTTCCAGG	84628
rs545791009	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132169943	CTGGGGGAGCTTCCT[C/T]GCCTGCAGCCCCAGC	84628
rs545794003	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199647	GAGGTCGAGCTGATA[C/T]TACATGGCCCAAGGC	84628
rs545851392	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233848	TTAGGAAGAAGCAGC[A/T]GGATTTTATGATATG	84628
rs545854392	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162879	GGCCGGCGTGGAGTC[A/G]AACCTGGAACTGAGC	84628
rs545861683	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132198688	TTATTGGATACCTGG[G/T]ATGTTACCTGGTATG	84628
rs545891113	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132163744	CAACTCCAAGAGGAA[C/T]CTGCTGGCGAGCCCA	84628
rs545943320	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216238	CTTCCTCCCTTGCTT[C/G]TTTCTGCAAACATTG	84628
rs545950822	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132200867	TTGTGGAACTGGTGT[-/C]CAGACTTTCAGCCCC	84628
rs545950930	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132175986	CAGCATAGCAATAAT[C/T]ATTTTAAAAAAGATT	84628
rs546022799	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168124	GCAGCCCAGGGGTGA[C/T]GGGTAAAGGCATCTG	84628
rs546037028	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177634	CTTACTTCTGGACTC[G/T]CAAATCTCTGGGTTT	84628
rs546061662	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160435	ATTCAGTGAATAATG[C/T]ACACAAACTGGTTTG	84628
rs546077152	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173793	GGTCGAACCATACTG[C/T]GGATGAGACGGACGG	84628
rs546137695	in-del	-/GACG	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132174311	CCATGCTGCGGATGA[-/GACG]GACGGACGGACGGAC	84628
rs546187377	snp	A/G	0.000141533	0.00841109	intron-variant	NTNG2	GRCh38.p7	9:132238967	AGGGTGGGAGGCCTA[A/G]GGCACCTTCCGGTAC	84628
rs546214204	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166674	AAACAACAAGTTCCT[C/T]GCTGTTTGCAAAGCT	84628
rs546222503	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132220164	GTCTGTGCTGATCCT[C/T]TCCTCATTTTAAAAA	84628
rs546247666	in-del	-/TCCTT	0.000493868	0.0157064	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231286	GCCAGGCACGGTCTC[-/TCCTT]TCAGCCTTGCAAACC	84628
rs546263912	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233179	CTGAGCCTGTGGTGG[A/G]CAGACAGAAGCAAAA	84628
rs546265896	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227565	CAAGGCCAAGTGCTG[C/T]GTGTTCAGCACTCAC	84628
rs546307623	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172887	GGCACCTGCCACCAC[A/G]CCAGGCTAATTTTTT	84628
rs546350195	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132185769	TGGCCAGTGAAGCCC[C/T]GAGTAGGGAGTGGGC	84628
rs546445189	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132238348	CAGCCTGAGAACCAC[A/G]TAGGGGTGGGGTGCA	84628
rs546528574	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170449	CCCCTGAGGTCAGCC[C/T]AGCAAGGCTGCAGGC	84628
rs546579021	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207677	TTTGGCCCACAGCAG[G/T]CACCTATGACATGCT	84628
rs546581062	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213898	AGGAAAGAAGGACCA[A/G]GCAATGTGATTAATG	84628
rs546621133	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235831	GCATGGTGGGGACCT[A/G]AGGTTGGAGGGGGGC	84628
rs546649053	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132194861	GAAGCCCAAAGGCTG[C/T]GGCTGCTGCAGTGGC	84628
rs546658231	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230228	CCCAAAAATCTGAAA[C/T]AAGAGGAGGAGTGCG	84628
rs546707938	snp	A/G	0.00755907	0.0610114	intron-variant	NTNG2	GRCh38.p7	9:132196503	AGCCTGGGTCTATGG[A/G]TTTTGACTCATTCAT	84628
rs546708864	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203043	CGGTGGGAGAGGGAA[G/T]TGGGGGAGGCTTGGG	84628
rs546787605	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225265	TTTTGTTTGTTTTTG[G/T]TTTGTTTTGTTTTGT	84628
rs546921375	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207146	AGGCATTTCCTCTGC[A/G]AGCTTTCTCGCCATC	84628
rs546954733	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242593	GTCCTGTTTTCTATT[A/C]TTTATTTTTCCTGCA	84628
rs547060375	snp	A/C	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132212205	TCGGGGGTGTTGGGC[A/C]TTCCTGCAGGGGAAG	84628
rs547094225	snp	C/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132181394	GGCATGATCTTGGCT[C/G]ACTGCAACCTCCACC	84628
rs547114242	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132211752	GCCTTGGCGGCTTGT[A/G]ACAATTCCACAGCCT	84628
rs547154420	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132181558	GACCTTAAGTGATCC[A/G]CCCACCTCAGCCTCC	84628
rs547164235	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176161	TGAGACCAGCCTGGG[C/T]AATGTAGTGAGACCC	84628
rs547194025	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193138	TAAGTAAGGCAGGAA[A/G]ATGAAGAGAGACCAG	84628
rs547196848	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176480	TCCTTCACTGGCAAA[A/G]TGTTTCCAAGGTTTG	84628
rs547205769	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170606	CAAGACACGTCTCCC[A/G]CCAGCCACCTGTGGT	84628
rs547242802	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170901	CTGGAGCGCTGGGGT[G/T]GGGTTGGTCCAGGAT	84628
rs547256208	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240074	TAGAGGCCAGGTCTC[A/G]GCCTCAGGGGCTGTC	84628
rs547272111	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132163173	GCTGCCGTGGCTTGC[A/G]CGCAACTTTGGGAAG	84628
rs547279421	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164917	AAGTGTCCGCCACTT[C/T]GGTTTGTCATTTTTG	84628
rs547328865	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132177948	AGGCGTGAGCCACAG[C/G]GCCTGGCCTCAAATC	84628
rs547370981	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174306	CCGCACCATGCTGCG[A/G]ATGAGACGGACGGAC	84628
rs547387047	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234657	CTGCGGGCGGAAAAC[A/G]CCGCTGGAGACACTA	84628
rs547446153	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132169745	GGCCGTGCTGCCGTG[G/T]TACGTGCGGACACAT	84628
rs547489272	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218245	TGGATTCAAGTCCTG[C/T]GTCTGCCCCTTACCA	84628
rs547576422	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200402	AAAAAGTGATTTGCC[A/G]TATGGCAGGTAGAGC	84628
rs547639008	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174005	GTCGAACCATGCTAC[A/G]GATGAGACGGACGGA	84628
rs547639948	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229026	TAGACAGGCCTGTAG[A/G]GGCTGGGCAGCTGGG	84628
rs547644591	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234930	GTATAATCCCTTCAA[A/G]AAGCGGAAAACAGCA	84628
rs547680676	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186123	TTTCAGCCCCACACT[A/C]GAAGGAGGGAGCAGT	84628
rs547685192	snp	C/G	0.00557542	0.0525036	intron-variant	NTNG2	GRCh38.p7	9:132234609	CCAGATGTTTCTCCC[C/G]CCTGCCAATGTCAAG	84628
rs547770154	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216711	GAGATTGATGGTTCC[G/T]GAGGGTCAAATTCAG	84628
rs547776383	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173907	GCGGATGAGATGGAC[A/G]GACGGACGGACAGAT	84628
rs547778310	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237856	GGACACACGGGTCAC[C/T]GATGCTGCTCTTTGG	84628
rs547788348	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207184	TTCACTCAACAGATG[A/T]TTTTTCTCAGACCTT	84628
rs547791237	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174792	CCGGGTGTGGTGGCG[C/T]GCGCCTGTAATCCCA	84628
rs547816339	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132238676	CGAGGATACCACGGC[A/G]AGCGCCGTGAACCCA	84628
rs547821071	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180270	GGTGAAGAAGAGACC[A/C]ATGAGAGATGAGCCC	84628
rs547846986	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204398	TAACTGGAGATGGAC[A/G]GACACCGGACTAGAA	84628
rs547865900	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132205286	CAGCCTTAAAAAGGA[A/G]GGAGAACCTGACACA	84628
rs547868557	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239471	GTAACCTACCCTTGC[A/G]GTTCTCCGGTAAGTT	84628
rs547940470	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214796	TCGTTGTTTTTTAGG[A/G]TAAGTATGTCCCAAA	84628
rs547951364	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185352	AGGATCTGGGGAGGG[A/G]ATCCGAGGAGAGGCA	84628
rs547986754	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132179682	AAGCACCCCATGTGT[A/G]CAGCTTTTTGCCCTC	84628
rs548013389	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222025	TCTCCAGCCAGCTCA[C/G/T]GGGGGTGTTAGATAG	84628
rs548035391	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208432	TGTGATCTGATTTCC[C/G]GTGTTTGGAAATCTG	84628
rs548063659	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132178825	GCTGGGTGTGGTGGT[A/G]CACACCTGTAGTCCC	84628
rs548148669	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189983	TTTAGCCTGTAATCC[C/G]AGCACTTTGGGAGGC	84628
rs548207431	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168188	TGATTCCAGCTTAGA[G/T]TGGCTCCAATGTCTC	84628
rs548213498	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190960	AGAGATAGGAAAGCT[A/G]TAGACATGATGGGCT	84628
rs548258575	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183211	GGGAGAGGGCCACTT[A/C]AGCCCTCACACTTTG	84628
rs548274747	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227782	TCTGAGGACCACCCA[C/T]CCGGGCGCGCTAGCG	84628
rs548326602	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201883	CCCTGGAGCGCTCCC[C/T]GCGGGGGCAGCGCTC	84628
rs548348371	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191426	TCACATGGCAATCAA[G/T]AAGAAAATAGAGACT	84628
rs548387493	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173119	CTGCAGTCCCTGTTC[C/T]GTGGGATTTGCGATT	84628
rs548425891	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132173664	CAGACGAACGGACAG[A/G]CAGGCAGGCCGCACC	84628
rs548428016	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167214	TGTCCCACCTTGGAA[A/G]TGTGTCAAAACAGAG	84628
rs548432612	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244812	GCGCTGGCCGCAGTC[A/G]GTAAACAGCAGGCAT	84628
rs548496900	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203914	CAGGAACAGGAAAGG[A/G]GGAATGAGTTCCCCA	84628
rs548501681	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196821	GTCGCACCACACTGC[C/T]CCCACCTCTGACGCA	84628
rs548569907	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132183944	TGCCACACCCCTCCC[A/G]TCCCCAGGTATTGTC	84628
rs548573312	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231148	GTCCCAGGGGAGTCG[A/G]ACCAGGGAGGGGCAT	84628
rs548630531	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171918	AGTCGGCAGATGTTT[C/T]CAGGTATGACCTCAT	84628
rs548709439	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178078	TTATAGATGAGGAAA[A/C]TGAGACTCCAAAACT	84628
rs548719345	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202284	AGAGGCACCTGGCTG[A/C]AGAGGAGGAGCTGGA	84628
rs548758100	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166643	TGGCTCTGAATTTTC[C/G]GTGTCGGCCTTTTGG	84628
rs548835799	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236420	ACTCTCCAGAAGGGA[A/G]ATTGTCCCTGGCCCC	84628
rs548872822	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132236967	ATGCCAAGTTTAGTC[C/T]CTGGGTTTGATGCTC	84628
rs548875846	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188361	TGGAACCCGAGTCTG[C/T]GGGAGCACAGTGCGG	84628
rs548909652	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176310	CCAACACGTTTCCAT[C/T]GCCCCAATAGAAAAC	84628
rs548914619	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182067	GAGAAGGGAGGGCCC[A/G]GAGGAGTGACGGTGT	84628
rs548937257	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176379	CCCTGAAAACCACGC[A/G]TCTACTTTTTGTCTC	84628
rs549001473	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234748	CAGGGCTGGCTTTCT[C/T]ATGGCTCTAATTAAG	84628
rs549065140	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132188366	CCCGAGTCTGCGGGA[C/G]CACAGTGCGGCCCAG	84628
rs549078534	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213434	ATCCATTGGCCACGG[A/C]CACCCACCGGCTGGG	84628
rs549102291	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164259	ATGCGTGGCATTTAA[A/C]CCAACAGGACTGCAA	84628
rs549208990	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230188	AGGAACACTCCATAC[A/G]ATGTCCCTGTCCTGC	84628
rs549222545	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229961	TTCAGGTCAGGCCTC[A/G]CCCACTCTCGGCTAT	84628
rs549244703	in-del	-/AAAAA			intron-variant	NTNG2	GRCh38.p7	9:132178787	CTCTACTAAAAATAC[-/AAAAA]AAAAAAAAAAAAAAA	84628
rs549245718	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225161	ACCTCAAGTTATCTG[C/T]CTGCCTTGGCCTCCC	84628
rs549305059	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182573	CGACCTTGGGTGGAC[A/G]CTGCGCCTCATCAGC	84628
rs549315274	snp	A/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132206674	TCCGTCTCAAAAAAA[A/T]AAATAAATAAATAAA	84628
rs549338614	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132193036	ACAGACAGGCCGGGT[A/G]CAACTGGGGGCTTTG	84628
rs549354444	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200629	TTCCAGCTTGTATTT[A/G]CATTTTGTTTCACTT	84628
rs549369063	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213767	GAGAAATTGGAAAAC[A/T]TTGCTGGCTGTGTTA	84628
rs549390594	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132211702	CTCCTGAAGGCTGGA[A/G]ACCTGTGCAACCAGC	84628
rs549427369	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206393	AACTCTTGGCCGGGC[A/G]TGGTGGCTCACGCCT	84628
rs549430617	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228140	TGCTCAGACCAGGCC[C/T]GGGCAGTGGCCTCCT	84628
rs549474863	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186826	ACTGCAGAGGGTCCT[C/T]GCTCAGTTAGGGAAT	84628
rs549494412	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194038	TCCCATTTAACCTCA[A/G]TCACCTCTTGAAAGA	84628
rs549500140	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233912	AAAAAGGGGCAGCTG[C/T]TCAAGGTCTCAGAAT	84628
rs549519949	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205187	GCAGCTTTATTCAGA[C/G]TAGTCAAAAGGTAGA	84628
rs549522519	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186782	TCTCCCCCAGGCAGC[C/G]TCCTACCTGGATAGA	84628
rs549559692	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234398	GACCGGGCTTCCATG[A/G]GGCCTTGGCACAGCA	84628
rs549572817	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132169941	GGCTGGGGGAGCTTC[C/T]TCGCCTGCAGCCCCA	84628
rs549586434	snp	A/G	0.0111196	0.0737302	intron-variant	NTNG2	GRCh38.p7	9:132174933	TCTCAAAAAAAAAAA[A/G]TGTATTTTTATTTTT	84628
rs549592963	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237382	CCCTGGGCAGTGGGA[C/T]CATGACAGACGAAAG	84628
rs549595321	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211340	AGGCTGGCGTCAGGA[A/T]TTGGTTTCGGGACAT	84628
rs549655990	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170466	GCAAGGCTGCAGGCC[A/G]AGAAGGAGGCAGGAA	84628
rs549662093	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213601	TCATCCTGCAGAACA[C/T]GCCAGCCTCCCTTGT	84628
rs549720214	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186368	CCACATATGCCCAGG[A/G]CAAAGCAGAATGTGT	84628
rs549743757	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132161937	TTTGCACTTGTTAGC[A/G]GCGACCTCCCGCTCA	84628
rs549749158	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179578	TGGTGGTGTGCTGGA[C/T]GCCTGGGAGCCTCAT	84628
rs549770758	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132228019	GTCCTTATTACGGTC[C/T]CTTCTCCAGATGAGC	84628
rs549827504	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190807	GCTCAGGCTTGGCAT[C/T]TGTGTAGGAGGCTCC	84628
rs549829094	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229314	TCAGTAAGTGGCACC[A/G]ACACCCACGGGGCCA	84628
rs549878423	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204525	CCCACCCTCCCTGCA[A/T]CTCTTTCTCAGCTGC	84628
rs549944729	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160831	AGGCCAGGAGTGTCC[C/G]AAAACCACATGTGCT	84628
rs549951335	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180795	CAGAAAACCCTGGAG[C/T]GGGAGCTTCTCACTT	84628
rs550023388	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233426	AGATTGTGCAAAGTT[A/G]GGAATTAAAGAGGAA	84628
rs550023994	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210499	TGAGAAGCTCAGTTC[A/T]TAGTAGGTATAGCCA	84628
rs550036936	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132239334	GGGTGCACTGCCCTG[C/T]GAGGTGGCCTCTGGG	84628
rs550075446	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239904	GCTGCTCTTCACCCC[A/T]GGTGGGCACCCAGTC	84628
rs550082842	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192249	GGTGGGGGGACTGGG[A/G]TAAACTGGTCTTCTA	84628
rs550087210	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233737	TCCTGGGCTGTGCTC[A/G]TATCATTGTATCATC	84628
rs550118401	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191363	AATAATCGCTCCCAT[C/T]TGGAGACATTTCCTA	84628
rs550160048	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244282	AGTGAAGGGTGGAGC[C/T]GGGGGTGGAAGTTGC	84628
rs550233733	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177858	AGATGGGGTTTCACT[A/G]TTTGGCCAGGCTGAT	84628
rs550235340	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209137	ATGAGTAGAGCTGCT[A/G]TAAACATTCGTGGAA	84628
rs550279362	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216252	TCTTTCTGCAAACAT[G/T]GAGCACCTACTGTGT	84628
rs550322787	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190859	CTATGGGCCTGGCTG[A/G]CTGCCTTCCCTTCCC	84628
rs550337261	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232153	TCCTGACATGCAGCC[A/G]AAGACTGGCCTTATC	84628
rs550359610	snp	A/G	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132184695	TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG	84628
rs550424268	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227238	ATGCACAGAAACACA[C/T]GTGCGTGCATGCACC	84628
rs550524680	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172140	TGGCCCGTGCTGTCT[C/T]CTCCACCCGAATGCC	84628
rs550529874	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240462	GGCCCACCCCGGGAG[A/C]AGGAATAGGCTGTTC	84628
rs550542070	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167129	TGGACGAGCAGAGCT[A/G]GAGGACTGAGATGCA	84628
rs550601579	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237815	AGGTGTGGCCCTGGG[C/G]CTCGTGTTGGTTGAA	84628
rs550671478	snp	G/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180091	AGTTTGTCTTGGGTC[G/T]CTCAGGGACCGTTTG	84628
rs550687052	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196890	CTGTAAATTGGGGGT[A/T]CCCACGACCCCTCCC	84628
rs550721717	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197555	GCTCAGAGGTACAAC[A/C]AGGCAGGGGCAGGAG	84628
rs550780832	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177170	TTTTGTGTTTTTAGT[A/C]GAGACAGGGTTTCAC	84628
rs550781010	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183760	GTCATCGTGTGGGGG[A/C]CCTTCCCTGGACCAC	84628
rs550804784	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172964	TCGATCTCCTGACCT[A/C]GTGATCCACCCACCT	84628
rs550827759	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214033	ACACTCTGAAATCCC[C/G/T]GTGGGGCTTTGCCTT	84628
rs550866401	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208362	AGCCCTGCAGCCCCG[A/G]GAGGAAGTTGGTTTT	84628
rs550888041	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132202224	ATTTCCAGCTCCAAG[A/G]GGGACCCCAATGGCA	84628
rs550915727	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196023	TGACCCTCCTGCCTC[A/G]GCCTCCCGGAGTGTT	84628
rs550937352	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181999	AGCCATGTGTGCTGG[A/T]GAGCATACTGTCCCT	84628
rs550942277	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236237	CCAGCCGGGGCAAAG[C/G]CTTGGCAGTGGGATG	84628
rs550944908	snp	C/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132235891	GAATGTCGGTGCCTG[C/G]GGAGCTCTAGGGCAC	84628
rs550964851	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189357	CATTGGTGAACATCT[A/G]TTTTGTATGCTAGGT	84628
rs550978023	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132176301	TACTTAGTCCCAACA[C/G]GTTTCCATCGCCCCA	84628
rs550980966	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231018	TCAAGAGTGGGGTGA[A/C]CTTCCCCCACCAGGG	84628
rs551014749	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176564	GCCATCCTGTGGACA[C/T]ACCATATTTTGTGTA	84628
rs551016614	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195444	CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCAC	84628
rs551135412	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194823	CAGGCAGCCAGGGGA[C/T]CTGTCCTTCACCCTA	84628
rs551142822	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171509	TCTCCAGCATACAGA[A/G]GCACCTTGGCTTTGG	84628
rs551142853	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171064	GGAGGGATGGAGCTG[A/G]GAGCCGAGATTCCCA	84628
rs551162061	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187551	TGAGAAACACACACA[C/G]AGAGAGCGAGAGGGA	84628
rs551165784	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212495	TGAACTCAATTGCCG[A/G]CCTGATTGCGTTCCA	84628
rs551187386	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132165091	TCAAATGCAATCATC[A/G]AAGACATATTAACCA	84628
rs551261783	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193957	GGCCCCAGCGTCTCA[C/T]CCGGCAGCCAAACTT	84628
rs551269174	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243449	GGAAGCTCCTAGATT[C/T]GGGGCTCATCCCCTG	84628
rs551273844	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193950	GCACATGGGCCCCAG[C/T]GTCTCATCCGGCAGC	84628
rs551276169	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234650	GACAGCGCTGCGGGC[A/G]GAAAACGCCGCTGGA	84628
rs551391438	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163277	ACTCGACCCTGGCCC[C/T]GGCCTCGACCCCGCC	84628
rs551430132	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132164085	CCCCCTTCTCTTTTT[C/T]CTTTTTGGCAGAACC	84628
rs551447623	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166762	CCATGCTGAGGCCGC[A/G]AGTCCCGCCTGACCC	84628
rs551478190	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132169865	GGCTCCTTTGCCTCT[C/T]CCCAGCCTTGGGGAC	84628
rs551556797	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240710	TGATCCCAAGGAAGG[A/G]AGCCAGAGTCTTCTC	84628
rs551564370	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132194780	CTGCCTCAATGAACC[A/G]AGGGTCAGCCCTGCC	84628
rs551600989	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132223185	AGGATAATTCGAGGA[C/T]AGAGAGAAGACCCCA	84628
rs551632415	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229447	CTGCAGCAGCCCTCA[C/G]TCCCGATGCCTTCCC	84628
rs551706644	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211644	TCCTGTCTGGCAAAC[C/T]CCTCACCCCTCAGGA	84628
rs551738626	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174854	TTGAACCTGGGAGGT[A/G]GGGTTTGTAGTGAAC	84628
rs551747353	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132233071	AGCCTCCTGACCCAG[A/G]AATCCTCTTTGGGGT	84628
rs551762348	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240169	CTGGCTGCCCAGAGG[A/T]GGGGCTCCTGCAAAG	84628
rs551783047	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170257	ATTCCAGCCTTGCAA[A/G]GAAGGGGAGGAGGCT	84628
rs551784386	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233409	GCCGTGGGAGGCTGG[A/G]CAGATTGTGCAAAGT	84628
rs551797673	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240253	CTAAGTGATCAAAGC[C/T]GCTGACGTCACAGGG	84628
rs551801368	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132214362	GCCCCTCCCTGCAGC[A/G]CAGGGCACGCTCCTG	84628
rs551825079	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228372	GGGGCTGACAGCCCA[C/T]TCCAGCCGCTGCCTC	84628
rs551840148	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199969	ATGGTTCTGTGTTGT[C/T]CTGGGTCATTTGTAC	84628
rs551858201	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132220849	CTTCATTCTTTTTAC[A/G]TGGGTCTCCCATATT	84628
rs551859897	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228767	TTTGCCATGTTGCCC[A/G]GGCTGGTCTCGAGCT	84628
rs551875397	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132163442	GCCGGAATTAAGAGG[A/C]CCGCCGAGGCTACAG	84628
rs551877038	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132239288	TGAGAGGGCACGGAC[A/G]CGGCACAGGGAACTT	84628
rs551887041	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192143	ACCCAGAGGAGGCTG[G/T]CAAACCTTCACCCCC	84628
rs551894708	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206331	CAAAATATTTGGAGA[A/G]TCCCTGGAAAGGCAG	84628
rs551929765	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200564	TGCCAGCCATGTGCT[A/G]TGGTGATGCCTGTGC	84628
rs551930091	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132201101	ACCTTTCATAAGGTG[G/T]CTCATGTGGGGCCCT	84628
rs552002920	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213442	GCCACGGCCACCCAC[C/T]GGCTGGGGAGGAGAA	84628
rs552017304	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180690	CTTCAGGGAGACGGA[A/G]AGAGAGAGAAAGAGA	84628
rs552029794	snp	C/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132215849	CCCATGTACTCTCAT[C/G]TCCGTCCCTCCCTCT	84628
rs552051762	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204505	TCAGCCACCCTATTC[C/T]TGTACCCACCCTCCC	84628
rs552114906	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191551	TATGGAAAATGGGTA[C/T]GTTAACTCATCTTTC	84628
rs552115311	snp	A/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230215	CTGCACTGGAGGGCC[A/C]AAAAATCTGAAATAA	84628
rs552119382	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211185	ACCCACTTCATGCTT[A/G]GGTTCCTGGAGGCCT	84628
rs552130602	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184632	CTGGCCAGTAGAAAA[C/T]GAGGCCAGAAGCCGG	84628
rs552176453	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171326	CTTGCCCACCTCACC[A/G]ACTTCCTGGGAGAGG	84628
rs552185061	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171455	CTTGACATTTCTACA[C/T]TGACATGGGTGAACA	84628
rs552267864	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209001	GGCTTATGGCGTGGC[C/T]GCCTGCGTGGCTCGG	84628
rs552344965	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179500	CAGGAGGGCAAGGCC[A/G]GGTAGGATGGTGGCT	84628
rs552373787	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221866	ATTCGGCCGGTCTTC[G/T]ATGCATCTTTACTAA	84628
rs552388896	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167977	CACTAAGAGCACACA[C/T]TCCTAGGGTCATTGT	84628
rs552401811	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132238695	GCCGTGAACCCAGGC[A/G]TCGCCCTCCCCCAGT	84628
rs552426405	snp	C/T	0.00835141	0.0640778	intron-variant	NTNG2	GRCh38.p7	9:132168247	GCTCCGGAGGCCGTC[C/T]CTGGCAGGGCAGGGC	84628
rs552463710	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160689	TGCTCCATTCCCAAC[A/G]CCCTCTGTGACCTTG	84628
rs552481499	snp	G/T	1.7063e-05	0.00292082	missense	NTNG2	GRCh38.p7	9:132198510	CCCTCACCGACCTGC[G/T]CATGCGGCTGCTGCG	84628
rs552492993	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190594	CACATTTACCTCCAT[C/T]CTTGCTAACAGTTCA	84628
rs552500439	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132161791	GGCAGTGAAGCGCCC[A/G]CCATCTGGCCCGCGC	84628
rs552539292	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166062	ACCTGGATGGATTGA[C/G]AGCTGAGATCTCAGA	84628
rs552590486	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173717	ATGGACAGACGGACA[A/G]ACAGGCAGGAGCACC	84628
rs552618021	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214980	CTCCTGGACTCAAGC[A/G]ATCCTCCTGCCTCAG	84628
rs552649095	in-del	-/TGAGCAAC	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189930	CTGGGATTACAGGCG[-/TGAGCAAC]TGTGCCCAGCCTAAA	84628
rs552661450	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213854	GTATACACGACATGT[A/G]ATAATGTGGGGACGG	84628
rs552711673	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196855	GCAAGTTCCTGCCTC[C/G]CGTACTTCTGTCCAA	84628
rs552730325	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237023	AGAGCAAGAGACGGG[C/T]GTGGTGTGCAATGTG	84628
rs552736655	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132238727	CACAGCCAGGTGGCA[G/T]GACCCTGCCCTCCTT	84628
rs552747678	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236509	TCCTTCCAGCTCACA[G/T]GTTCAAATTTCCTCC	84628
rs552767207	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171187	AGAGCTACAGGCCTA[A/G]AATCTGAAGCCCTGA	84628
rs552799635	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165678	AACAACTTTGACATT[C/G]TGACTTGACAGTCAT	84628
rs552827594	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132196269	GATCTCGGCTCACTG[C/T]AACCTACGCCTCCAG	84628
rs552835849	snp	C/T	0.000399281	0.0141238	intron-variant, missense	NTNG2	GRCh38.p7	9:132231520	AGTGAGCCGAGAGGG[C/T]GCCAGAAAGAAGCTG	84628
rs552870581	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226739	AGGGTTTCTTCCTGG[A/G]CAGCCCAACACCCTC	84628
rs552898133	snp	A/G	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132236465	GGGTGGGGAATTAGG[A/G]CCTGAGGTCTAGGGA	84628
rs552928781	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243067	CCTCCCCACACTGAA[A/G]GGCTGCCTCCCTCCT	84628
rs552950809	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236023	ACCAGCACTCCCTCC[A/G]AGGGCTTCGGAGTCT	84628
rs552983227	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132235670	GACCAGGCCATCTAC[A/G]GCTGCCCCTCTCTCG	84628
rs553025847	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242268	CCCGCGCTCCCGCCC[G/T]CACTGCCCTCCCCCC	84628
rs553032621	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132195579	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	84628
rs553058635	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230473	TTGAGGGAGCGACAC[C/T]TCCAGGTGCTCCCCT	84628
rs553112600	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176335	GAAAACCCTGCACCC[A/G]TTAGTTACTCCCCAT	84628
rs553158474	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217999	ATCGCTCCTCAGGGC[C/T]AGTGTCACTGGTGTG	84628
rs553207038	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229205	TGTCCTCAGCACCCA[A/G]GTCTCCTGCCTTCTC	84628
rs553229791	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175812	CCAACTGAGCAGCCG[A/G]GGAAGATTTGGCTAG	84628
rs553251192	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212609	CCCCTCTGCCCCCAC[A/G]GCTCTGTTGTTGGTT	84628
rs553289805	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132206942	GACCCCTGGACCTGC[A/G]GTCTCCTCTGGTCTT	84628
rs553298564	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182008	TGCTGGTGAGCATAC[C/T]GTCCCTGTCAGCCTC	84628
rs553389312	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132218114	CAGGCCACACAGCTG[A/T]GTGCACCATGAGCTG	84628
rs553396143	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159894	GGATTGATGACCATG[C/T]CCTGGGGTGACAGCA	84628
rs553399051	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210786	CTGGGCTGCCTCCCT[C/T]CACATCTCAGCAGAG	84628
rs553399343	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217004	CCCATGGAATGGACG[C/T]GAAGCCAGCACTGAG	84628
rs553402796	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224577	TACTCACTGTTCCCA[G/T]CTCAGAGCCCCTGCC	84628
rs553405794	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132188375	GCGGGAGCACAGTGC[A/G]GCCCAGGCAACAGCG	84628
rs553437956	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211370	TGACTGGCCTCCCTC[C/T]CTCCCTTCAGTCTTG	84628
rs553441579	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218475	GCACAATGTGATAGC[A/G]TTTTGTTTTTTTGTT	84628
rs553474244	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182092	CGGTGTTCCCCACCC[A/C]CTGCCCTTTGAGACA	84628
rs553494473	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206433	ACACTTTGGGAGGCC[A/G]AGGCAGGTCCATCAC	84628
rs553506201	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132212094	ACCCACCCTTGTCGC[C/T]TCCCACCCTTCCACC	84628
rs553517588	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192389	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTTGCCA	84628
rs553517718	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185687	TTCTTCTCTCCCGTT[A/C]TTTCATCCTTCCATC	84628
rs553530788	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132204989	CAAGTGTTGGCAAGG[A/T]TGTGGAAAAATCGGA	84628
rs553539454	snp	C/T	1.73866e-05	0.00294839	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240902	CGCCCGTGCCCGTGT[C/T]CGTCCAGAGTGTAAC	84628
rs553554724	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132186500	TCGGCTGACGGAGGA[C/G]ATCAGTCATTCAGGG	84628
rs553631586	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164492	TCCCTACCTGTTAGT[A/G]AACAGTTAGGAGTCG	84628
rs553649700	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132167557	GGAGGTTTGACGGAG[G/T]CTCAGAGGGGATTCA	84628
rs553692818	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193548	TTCAGTGCTGGGTTG[A/G]TAAGAGCTTTCTGGG	84628
rs553710639	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180884	CACACGTGTGTGCAA[A/G]CACTGGGCTCATGCA	84628
rs553740897	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168413	CCCACCTCAGAGTCC[A/T]GAGGACTTGATCTCA	84628
rs553747691	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175110	GGTTCGTGCAGAGAC[A/G]CAGGGAAGGGGGCCA	84628
rs553815844	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169424	TTCTAGATAGATCTG[A/G]GTTCAAACCCTGATG	84628
rs553824347	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132180402	GATGGCCAAAAGCAG[A/G]TGGCAGCAAGTGGAG	84628
rs553835710	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132221412	CAAACACCATGTCCA[C/T]ACACACCGACACAGA	84628
rs553842474	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204809	GGCTGGGTGTGGTGG[C/T]TCGTGCCTGTAATCC	84628
rs553852654	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162783	TGAGTTGCACAGAGA[A/G]ACTCCCGGCCAGTCC	84628
rs553854579	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223748	CCAGGCCTCTATTCG[C/T]AGGATCTCACTGATC	84628
rs553854617	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169990	CCACCAGGGGGCGCC[C/G]TAATGGCGGCCAGAT	84628
rs553877798	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191639	TGCAGTGGCGCGATC[G/T]CGGCTCACTGCAAGC	84628
rs553928842	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228095	GAGTTGCATGCCAAC[A/G]CCAGGGCTTAGGGCA	84628
rs553961733	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173764	GGATGGACGGACGAA[C/T]GGAGAGGCAGGCAGG	84628
rs553997911	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168073	CACGCAGATGTTAGC[C/T]GTTGTCATTCTGGTC	84628
rs554052027	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179197	GTGCCCTGGATCTGA[C/T]TTCACGTGATGGCAT	84628
rs554125494	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160340	CCACAATCCTTAGCT[A/C]TGTGACCTTGGGCAA	84628
rs554138874	snp	C/T	0.000399281	0.0141238	intron-variant, missense	NTNG2	GRCh38.p7	9:132231742	CTCCTGTCCCCTCCA[C/T]GTCCACTGCCTGGGC	84628
rs554227773	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132238945	CTCTCTTCCTGAATC[C/T]GATGGAAGGGTGGGA	84628
rs554264988	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233146	TTGGCCCAGCCACAA[A/G]GGACCTGTGCTTTGC	84628
rs554336983	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132227254	GTGCGTGCATGCACC[C/T]CCACACACACACCTT	84628
rs554363724	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236682	GGAGACAGAGCTGGC[A/G]GGAGCCATCGCTTCC	84628
rs554375590	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221619	CTGGGGCTCAGCCAG[C/G]GAGTTGAAGAGGCCG	84628
rs554375989	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132168749	TTCTCCACACGCTCT[C/T]GGGCACGGTCAACCT	84628
rs554400502	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231276	CTCACAGGGTGCCAG[A/G]CACGGTCTCTCCTTT	84628
rs554407952	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132187596	GAGAGAGAGAGAGAG[-/AG]GGACAGAAAACAAGA	84628
rs554410620	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184728	CAGGAGTTCGAGACC[A/T]GCCTGACCAACATGG	84628
rs554470849	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132204237	CCAAGCCCGGCTCCT[A/G]CAGACCCAGCTTCCC	84628
rs554473569	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244339	CAACCTCTGCACTGC[C/T]TTTATTTATCTACTT	84628
rs554617670	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193598	CCACTTGGTGCCAGC[A/G]TACTGAGAAACCAGG	84628
rs554619720	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221257	CAGGCAGAGGGAACA[C/G]CATGTGCAAAGGCCC	84628
rs554673740	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132177239	CGATCTGCCCGCCTG[A/G]GCCTCCCGAAGTGCT	84628
rs554711611	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195558	GGTGTTGATCTCCTG[A/T]CCTCGTGATCCACCC	84628
rs554716855	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214560	TCATCCATTCAAGAA[A/G]AAGGGAAACTTAGCT	84628
rs554734963	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226180	CTTTCGGTTACCCCG[A/G]GGTACAGTTTATATA	84628
rs554742665	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243830	GACTCACAGTGTCCC[A/G]AGCCCACACACCAGC	84628
rs554748184	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188934	GAAGCTGAGGCTCTC[G/T]GGCAGGAGAAAGATC	84628
rs554749028	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207445	CTCTGCCTTGTCTTG[C/T]GGCTGTCCGCTCCCT	84628
rs554788715	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166759	TTTCCATGCTGAGGC[C/T]GCGAGTCCCGCCTGA	84628
rs554812615	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166381	CCGTTGTGTTGAGCA[C/T]GTCACCCATTAAGAG	84628
rs554820351	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132215752	GGGTGGGTGTTGGAC[A/G]GGACAGCATGAATAA	84628
rs554833128	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188551	TTCCTGAGGATCGCA[C/T]TCTCCAGGATCCCTG	84628
rs554841023	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132168673	GCTGGGCTCTGGAAG[C/T]CAGGAGGAAGGCCAG	84628
rs554848588	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132219341	ACTTTGGGAGGCCCA[A/G]CTGGGAGGATCACTT	84628
rs554899612	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200996	CTGGGAACCAGCTCC[C/G]CAGGCCCTGCAGGCT	84628
rs554925863	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171109	TTGCCAAGGCGGGGG[C/G]TCTGTGCTTCTGAGC	84628
rs554936620	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132197094	TCCTAAGGGTACAGG[C/T]AAAAAGGCTCAGGGG	84628
rs554981325	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176890	TCTTATTAGGATGAG[C/T]CTAGTGGGTGTGGGG	84628
rs555012026	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171784	CCTCCTGCCAGACCT[C/T]GAGGATCATGAAATG	84628
rs555038063	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201528	AGACACAGGACTGGT[A/G]GCAAAGGGGGATGTG	84628
rs555151354	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132175733	AGAGTGAATGCCACC[A/G]GGAGTCAGAGTGCTA	84628
rs555197828	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235982	TTCAAGAGGTTCCAT[A/G]TGGCACCCCCACGCC	84628
rs555285414	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132182844	GGCTGGCTCTCAGCC[A/G]GGGTGCACACTGGAC	84628
rs555288818	in-del	-/AG	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132187551	GAGAAACACACACAC[-/AG]AGAGAGCGAGAGGGA	84628
rs555290904	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132170702	TCAGGGGTGAGCTGA[C/T]GAGCAGGTGAGAGAG	84628
rs555355834	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211916	GTATATGTGTGGAAT[G/T]CATTCATTCATTCAG	84628
rs555406393	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242113	GCCTGGGCCGCTGAG[A/C]CCCGCCCGGAGGACG	84628
rs555474346	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234287	CCCGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTC	84628
rs555493093	in-del	-/CCA	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132169604	AGCCAAGGCCCATGC[-/CCA]CCACCCACCAGGCGG	84628
rs555513182	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229175	CAGGGTCACAGGTGA[C/G]GCTGGAGGCGCTGCT	84628
rs555561962	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239641	CTGGGGCTGGTGTGT[G/T]GGGGGGTCCCCCTCC	84628
rs555574591	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187177	GGGGGAGGAGCAGGG[G/T]CGGTCGCCGTGGCTT	84628
rs555639665	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205406	GACGTCCCCAGAGTC[A/G]TCAAATTCATAGAGA	84628
rs555649136	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132217971	TGTGGGTGATGTGGC[C/T]GGTGTGGTCCATATC	84628
rs555668737	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169290	TACAAATGTGTGTCC[A/G]ATGAGGACGGGGAGG	84628
rs555706880	snp	A/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162537	TCGTGTGTGTGAGAG[A/T]GTGTGTGTGTGTGTG	84628
rs555717139	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184419	GGGGACACACCCGTC[A/G]TTAACCGAAGAAGCC	84628
rs555720138	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212562	GGAAAAGCCAGGCTG[C/T]GCCAGGCGACCAACC	84628
rs555725519	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224106	CTTCTTTGCACAACC[C/T]GTGGGCTCTTTTAAC	84628
rs555729522	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132184356	GGAGGGGGAGTCACT[C/T]GGCTGTGTCAGGCTC	84628
rs555747782	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132181673	AAACATCGAGCATTT[A/G]TTGAGTGCCTCATGT	84628
rs555758050	snp	C/G/T			intron-variant	NTNG2	GRCh38.p7	9:132203034	CTGGTTAGACGGTGG[C/G/T]AGAGGGAAGTGGGGG	84628
rs555786848	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216188	GCAGGTGCTCCATGC[C/T]GGTTGCTGCACACAG	84628
rs555787187	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222707	CACGGCCCACCCAGG[A/G]CCTGCAGGATTCTCT	84628
rs555788930	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132235969	CAAGCTCACCTGCTT[C/T]AAGAGGTTCCATGTG	84628
rs555824041	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216510	TGAAGAGCTAAAGCC[A/G]TAGGATTCTGCAGTG	84628
rs555871412	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132223559	GCCAGTTACACATCC[C/T]CAAAACAATCTCTGA	84628
rs555910025	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223974	CCCTAGGGCTTTCCT[C/T]ATGCTCTTGCCTCTT	84628
rs555984625	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132163560	CGCCACTCTCCCCTG[A/G]AAGCAGATTTCACCC	84628
rs555984845	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233654	CCTCCCTCCTCTTCA[A/G]CAACTGAAGCCCCTG	84628
rs556005441	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205781	ACCTACTTGGGAAGC[C/T]GAGACAGGAGAATCA	84628
rs556033664	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132202420	GGGCAGGTGGGCTGC[C/T]GGTGGCTCTGAGAGA	84628
rs556050157	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222333	GTACCAATAGGTGCC[C/T]GCTGTCCCCCTCTGT	84628
rs556114524	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200040	CTACCCTGGGCCATC[A/T]GTAGAATGGGGATGG	84628
rs556121472	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132233100	GTGGAAGACATGGGT[C/T]ACTCTGAGAATTCTG	84628
rs556126886	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192607	AAAAACAAAACAAAA[A/C]AAAACAAGAATAGAA	84628
rs556165506	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179854	CACAGGAGTTCGAAT[A/G]GTCGTTCTGAAATTG	84628
rs556180538	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191603	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	84628
rs556202565	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174094	CGGACAGATAGGCAG[G/T]CCGCACCATGCTGCG	84628
rs556202576	snp	A/T	0.00874735	0.0655527	intron-variant	NTNG2	GRCh38.p7	9:132180338	TGCTGCCAGCCTGCA[A/T]CAGGGCAGTGTCCTT	84628
rs556205539	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179844	CCTTCTGTCACACAG[A/G]AGTTCGAATGGTCGT	84628
rs556208145	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210254	GTTTCCCCACCTGTA[A/G]AATGGGATCCCGCTC	84628
rs556254922	snp	C/T	0.0150606	0.0854603	intron-variant	NTNG2	GRCh38.p7	9:132192361	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA	84628
rs556256692	snp	A/C	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132197912	GCGCAGAGGCTTCCC[A/C]GGCCATCCCGAGCAT	84628
rs556303048	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168022	TTAATTAACGTAGGT[A/G]AAGTGTTCGGAATAG	84628
rs556309564	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132177475	GAGTTAATTTTTGTA[G/T]CTGGTGTAAGGGAAA	84628
rs556321049	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132232484	TCGCTCCCCTCCAAC[A/G]GAGGGATTCACGTGT	84628
rs556323742	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209032	GCTCCTCACTCCTGA[A/G]TAGGACTGTGCCGTG	84628
rs556350462	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132178328	CCTCCAGTCCACCTC[C/T]GTCCCTCTCCCACGC	84628
rs556360046	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227427	CCTTCTTGACCCTGA[A/G]GGCTGGCAGGTGGCC	84628
rs556383585	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176659	TGTGGACATTTGGGT[C/G]TCAGTTTTTGCATGT	84628
rs556417197	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132184951	CTGGAAAGACAAGGG[A/G]GAGAGGCAGAGCTGG	84628
rs556489042	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173310	CACAGTGAAGTCTCC[C/G]TCCTGGGCAGTAGAC	84628
rs556499894	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174448	GGAGGAGATGGGGCC[C/T]GGGGGCATCCCGCAC	84628
rs556583978	snp	C/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132215081	TTTGTAGAGATTGGG[C/G]GGGGGGGTCTCACTT	84628
rs556670314	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183379	CTCCTGGCTCAGCAG[C/T]GTGCATGCGTTAACC	84628
rs556739379	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243190	ATGCTCTGATTTATA[C/T]TGTGTCTCGGTGGCC	84628
rs556782923	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132214444	AGCTGGGCCTGCCAC[A/G]TTTCCCAGAGAACTG	84628
rs556820004	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208568	CCGCCTGGAGGTGGT[C/T]TTTGGTGGCAGTGTT	84628
rs556824326	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132221142	TGATTTGAGGTAGGG[G/T]TTGTGAAAGGCCTCC	84628
rs556935298	snp	C/G/T	0.00159649	0.0282165	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166716	GTCCCTGGGACACCC[C/G/T]GGCCACCCTCGCCTG	84628
rs556962273	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225400	CCTAGCCTCTTGAGT[A/G]GCTAGGACTGCAGGC	84628
rs556992306	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195735	CCTGGGCTCAAGCAA[G/T]CTCCAGCCCCAGCCT	84628
rs556999245	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219197	ACTCAGCCTGGGTGA[C/T]AGAGCAAGACTCTGT	84628
rs557014694	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189473	AGACCTGTGTGTCCA[G/T]GTCCCTCTCTGTGAC	84628
rs557060076	snp	A/G			intron-variant, missense	NTNG2	GRCh38.p7	9:132208780	AAAGTGGACCTTTTG[A/G]GGGTACAATTCTAGG	84628
rs557066893	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132226322	TGACGGGGGTGTGGG[A/T]GTTGGGGGTTCTATC	84628
rs557085183	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201469	TACCTCCCCTTTTCC[C/G]TCTTCAGTTCCGCTG	84628
rs557104830	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171769	GTCACAGACACTCTG[C/T]CTCCTGCCAGACCTT	84628
rs557143048	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132212642	TCGCTTTCTCAGGAT[C/G]TCAGGTTTGAATGGC	84628
rs557181153	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132172158	CCACCCGAATGCCTG[C/T]CCCCTCCTTCCTTTC	84628
rs557226929	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194506	GAGGAAGCTGGGAAC[C/G]CCCCCGCCCCATGTC	84628
rs557310243	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202588	GCCTGGAGAGTGGCT[A/G]GCTTCAGACTGTGCA	84628
rs557365349	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182178	GCAGCGAGCGTGCTC[C/T]CACGCACCAGCTCTG	84628
rs557368388	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188053	CTATTGATTTATGCA[C/T]CTGCCCAAGCCATAG	84628
rs557432157	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132213195	AGCATAGTGGTGCAT[A/G]CCTATAATCCTGGAA	84628
rs557445320	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200819	TATTCAAAATCAGGA[A/G]TGTTCTGGAAACCAC	84628
rs557502474	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180437	CTGTTAATCCAGAAC[A/G]CACCTTGTCTCTGCC	84628
rs557542649	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132180927	CACACATATAAGGTT[C/G]CAAACACTTTCAGGG	84628
rs557544666	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235479	GTAGATGCTGCCTAT[A/G]TAGTAGATTTGGACC	84628
rs557575750	snp	C/T	0.00517822	0.0506191	intron-variant	NTNG2	GRCh38.p7	9:132191128	GGGTGCAGGGAGGAG[C/T]GGCTGTGAAGTGCCC	84628
rs557587464	snp	A/C	0.00537904	0.0515809	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132241926	AACGGAGGCACCTGC[A/C]TGCAGAACCAGCGCT	84628
rs557604779	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241173	AGACGGGGCAGGGCC[G/T]GGGAAGTGGGTGGGG	84628
rs557713494	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175597	GGTCTGTTCGGCTTT[A/G]GTTTGCAGGATCCGA	84628
rs557722915	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162404	AAAAGTTGTTTGGTG[G/T]CGGCTGCTACGAGCT	84628
rs557724992	snp	A/C/G	0.000122754	0.00783339	missense	NTNG2	GRCh38.p7	9:132226962	GCAAGAAGAATTTCC[A/C/G]CACCCGGTCCTGGCG	84628
rs557750063	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170626	CCACCTGTGGTCCCC[A/G]TGAGAGGAAGGGGGA	84628
rs557772345	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211809	TACACGTCTGACACC[C/T]GCCCCCATAGGCTCT	84628
rs557772735	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211398	TTGCCCTTTCTGTAG[C/T]TTTTTGTCCCTAAAC	84628
rs557807956	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132163768	GAGCCCAGCCAGCTC[A/G]GGAGGCGCTAATTCA	84628
rs557840834	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164532	AGAATTAATTAGGAA[C/T]GTGCTGTGCTCTGGG	84628
rs557844244	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239501	TTTGCACTGGAGTTG[C/T]AAAACTTACCAGTGG	84628
rs557867839	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186573	GCATTTCATCCTTGC[C/T]TTCTGACCTTGGCTT	84628
rs557872541	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234386	TCCAAAGGAGCAGAC[C/T]GGGCTTCCATGGGGC	84628
rs557889578	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132187817	AGGGGAGGAGGATGT[G/T]TCTCTGTGCCCTTCC	84628
rs557983037	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161058	GGCCCCTCCTGCCCC[A/G]CTACTCTGCACTCCC	84628
rs558010803	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132223328	GCGGCCCCCAGGGGA[C/T]CCTTCATTCCCACTC	84628
rs558046469	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174018	ACGGATGAGACGGAC[A/G]GATGGACGGACAGGC	84628
rs558085419	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168535	GTGGTGGCTGGGCCA[A/G]GGCCAGCTGGGGAGA	84628
rs558121996	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132227288	CTACAGCTCCCAAAC[A/G]CCAGGTCTCATAACA	84628
rs558160702	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227789	ACCACCCACCCGGGC[A/G]CGCTAGCGTAGTCCA	84628
rs558184411	snp	A/C	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132234146	CAATTCTCCTGCCTC[A/C]GCCTCCCGAGTAGCT	84628
rs558193358	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216968	TCTGGCTTAGTGGCC[C/T]CTTTCCTGGCCTTCT	84628
rs558195484	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132189255	TAGTTTTCTTTTTTG[-/T]TTTTTTGAGGTTTTT	84628
rs558233791	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228518	GGGCCGCTCTCTCTT[C/T]CCTCCTCTCTGTCTC	84628
rs558336874	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222162	TTAATCTGCTGAGAT[A/G]TATTATGACCCTCAG	84628
rs558344612	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132231809	GTGCCAGGGTACAGC[A/G]ACCCCTGTCATCCCA	84628
rs558345803	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203423	ACCTATGGTACCAGC[A/G]GAAGCGATAGGGAAG	84628
rs558372173	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187179	GGGAGGAGCAGGGGC[A/G]GTCGCCGTGGCTTTG	84628
rs558384160	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232271	CCCTCAGCAGCACAC[C/T]GGTGGGATGGATGGA	84628
rs558427016	snp	A/G	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132209976	GTGGGCGGAGAGCTG[A/G]CAGGACAGAGGGCCC	84628
rs558441710	snp	A/T	0	0	intron-variant	NTNG2	GRCh38.p7	9:132198690	ATTGGATACCTGGGA[A/T]GTTACCTGGTATGTG	84628
rs558455838	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132208461	TGAGTTGGGGGTGGC[A/G]GTGCTGGAGGCCTGC	84628
rs558467599	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210626	GACACCCGGCAGGCT[C/T]CTGTCCCCCCGACCC	84628
rs558467647	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204849	GGGAGGCTGACGCAG[C/G]AGGATCTCTTGAGTC	84628
rs558489544	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237949	CTAGGTGGCCCACAG[A/G]TGGGAGTGCCCACCA	84628
rs558490204	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132184950	GCTGGAAAGACAAGG[C/G]AGAGAGGCAGAGCTG	84628
rs558500515	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205362	AAGCCAGACACAAAA[A/G]GACAAGTACCATATG	84628
rs558584809	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132215396	GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCAT	84628
rs558603331	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132191040	GGGTAAGTGATGTGC[A/G]GCCATGGGTACTTAG	84628
rs558617341	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132241796	GCCCCCGGGATCTCG[C/T]ACACCCTGCTTCGCA	84628
rs558659845	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132173800	CCATACTGCGGATGA[A/G]ACGGACGGACGGACA	84628
rs558669989	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197203	AGACCAGCCTGGCCA[A/T]CATGGCGAAACCCTG	84628
rs558688237	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182880	TGGGAGCTTTTCATT[C/T]CCCCCCTGCCGCAGC	84628
rs558691209	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189443	TCCTGGTGATAAACT[C/G]GCGGGAATTTTGCAA	84628
rs558692844	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173133	CTGTGGGATTTGCGA[C/T]TGGATGAAGCCGGGA	84628
rs558721331	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132214333	GCCCCCGCAGCAGCT[C/T]CCAGGCACTGCCTGC	84628
rs558729718	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132183345	CCCTTTGGCCTTCTC[C/T]CCTGCGCTCCCCACC	84628
rs558767570	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238984	GCACCTTCCGGTACC[C/T]TTTCCAAAGATGCCT	84628
rs558814095	snp	A/C/T	0.000798403	0.0199641	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160071	GTAACCAGGGGTGGG[A/C/T]CCATGTCTGCCTTCC	84628
rs558815799	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237819	GTGGCCCTGGGGCTC[A/G]TGTTGGTTGAAGCAG	84628
rs558878498	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225652	ACATTAGTATCTAAT[A/G]TAGGCAATGTCCAAA	84628
rs558885261	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188219	GCCTCTCCTGGGCAG[A/C]CTCCAGCCTTCCACC	84628
rs558888259	snp	A/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132172565	CCCTGGACTGTGAGC[A/T]CCTCAAAGGCAGGGC	84628
rs558960785	in-del	-/AGA	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132173330	GGGCAGTAGACAATG[-/AGA]AGACCGAGGCCCGGG	84628
rs558989714	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220990	AAAAACATACTGTGT[A/G]TTCAAAAACAAATAA	84628
rs559009146	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166777	GAGTCCCGCCTGACC[A/C]CGTCGCTGCCTCTCC	84628
rs559049745	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132167339	TATAGTATTCAGCTC[C/T]GCAGCCTTCAGGCTA	84628
rs559102946	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170775	CCTGCCACTCCCACT[C/T]AGAGCAATCGCCTCA	84628
rs559115179	in-del	-/TCTGTCCT	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132235325	GGGACCTGGTCTAGC[-/TCTGTCCT]TCAGTCAGAACGGGG	84628
rs559135524	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218323	CCCCATCTGCACAAC[A/G]AAGATAATAATGACA	84628
rs559140194	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164732	CAGCCAGAGGTGAGA[C/T]GGGGAAAATGGTCCT	84628
rs559155799	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185641	CTCTCGGTGCCTTTC[C/T]CCCGCCCGCCCCCTT	84628
rs559170613	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220183	TCATTTTAAAAACTG[C/G]ATTATTTGTCATTTT	84628
rs559205242	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213737	TCACCCAAAGATAAA[C/T]GCGCTATCTGGCAAG	84628
rs559217966	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176164	GACCAGCCTGGGCAA[A/T]GTAGTGAGACCCCAT	84628
rs559240106	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177308	AAATTTAATGAACTC[C/G]AATGTGTGTATTTTT	84628
rs559323687	snp	A/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132200489	AACAGACATTGGCTG[A/T]AAGTGTGTACAGGAC	84628
rs559327584	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180308	TCCTGCCCTCCACCA[A/C]GGCAGGCCATCCTCT	84628
rs559368925	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229818	TCGGGAACACCGTGG[C/G]GAAAGCTGTGGCACC	84628
rs559373928	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193906	GCCAGCCGCCTTCTC[A/C]CTGTGCCTTCAAACG	84628
rs559407508	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230122	TCCACCCGCGGCAGC[C/T]GCTCCCATGGCTTCT	84628
rs559520664	snp	C/G	0.00438332	0.0466095	intron-variant, missense	NTNG2	GRCh38.p7	9:132241487	ACGAGAAAGACCGAG[C/G]TGGGGTTGGTTGGAA	84628
rs559590362	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234641	TGTCTGGAGGACAGC[A/G]CTGCGGGCGGAAAAC	84628
rs559625808	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132206599	TTGAACCCAGAAGGC[A/G]GAGGTTGCAGTGAGC	84628
rs559661704	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181118	AGACAGGGTCTCACT[C/T]TGTCACCCAGGCTGG	84628
rs559689699	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223586	CTGAATGGACGAGAG[A/C]CAGTCAGGGGGAAAC	84628
rs559699357	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175320	CGCTCGCTAGGGTTA[C/G]GAAGGATTAGGCCAC	84628
rs559726767	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132217408	GAGTCTATCCAAGAG[C/T]CAGCACACTGAGACT	84628
rs559730034	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132220222	GTTATAAGTGTTCAT[C/T]AGATGTTCTAGATAT	84628
rs559752725	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199522	CAATGCTTGTGAACT[A/G]TCACCAGGCAGGGAT	84628
rs559822625	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132180597	AGTCTCTTCCCATTT[C/T]GGGGTATAGACTTCC	84628
rs559836352	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188379	GAGCACAGTGCGGCC[C/T]AGGCAACAGCGTCCT	84628
rs559887256	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206312	CAAAGGGGGTCCATG[A/G]TCCCAAAATATTTGG	84628
rs559907196	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161502	TTAGGCAGCGACCCC[C/T]CAGAGGCTGCCGGGG	84628
rs559938300	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186124	TTCAGCCCCACACTC[A/G]AAGGAGGGAGCAGTG	84628
rs559943591	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215645	CCTCCAAGAGGCCAG[A/G]GGGTGTGTCACCTCT	84628
rs559979001	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132198811	GGTATGTGATACATC[A/G]TTACCTGGTTCCCTG	84628
rs559980422	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209487	CTGCAGCCCTGAGAT[C/G]AGAGACAGGGGGAAT	84628
rs559987891	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216205	GTTGCTGCACACAGA[A/G]CTCCCATGCATTATC	84628
rs560073979	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160633	GGGTTAAGGTGGAGG[C/T]GAAGGGTGGCAGCAG	84628
rs560075806	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132191650	GATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG	84628
rs560081291	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221859	TTCTTGGATTCGGCC[A/G]GTCTTCTATGCATCT	84628
rs560163156	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132166125	CAAGGTCAGCTGGGC[C/T]CCATTAGTGCCGGCC	84628
rs560203215	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132191216	TGAGTCAGCCGTTCC[C/T]GGGACAGTCCACGCC	84628
rs560206279	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132186052	AAGTGTTTACAGCAT[A/C]GCCAGAGAAAAATAG	84628
rs560206937	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171336	TCACCGACTTCCTGG[A/G]AGAGGAAACGCCTCT	84628
rs560216519	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199474	AGTGGGGTTGTGCAG[A/G]CAGCACTTGATTCTC	84628
rs560234966	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239698	AGCAGCCTATCCCTC[C/T]TCCTGCAGGGGCCCA	84628
rs560302667	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191976	TAAAGAGGCAGCTAC[A/T]ACTTCTGATACTATC	84628
rs560328374	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167734	AGAAGGAGGGGTCCT[A/G]GGGGCACGGAGTACT	84628
rs560342226	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132212946	ACCCCCCAAAGAAGA[A/C]CAAGATCCCCAGGCC	84628
rs560369259	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191696	CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGACTA	84628
rs560390492	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173893	GGCCGCACCATGCTG[C/T]GGATGAGATGGACGG	84628
rs560397682	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204404	GAGATGGACGGACAC[C/T]GGACTAGAATAGAAA	84628
rs560400163	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196833	TGCCCCCACCTCTGA[C/T]GCAATTGCAAGTTCC	84628
rs560409394	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184996	CCAGGGTTTGGACTT[A/T]AGAAGGGGAAGGCGC	84628
rs560437091	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197416	AAATTAAAATTAAAA[A/G]ATAAAAGGCTCAGGA	84628
rs560440718	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132174125	GATGAGATGGACAGA[C/T]GGACAGATAGGCAGG	84628
rs560451667	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226715	CTAAAGGTTGGGCTG[A/G]TGGCCTCCAGGGTTT	84628
rs560539956	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244525	CGGTGATGTGATTAA[A/G]ACACTAGAATTTGGG	84628
rs560550823	snp	C/T	0.000399263	0.0141235	intron-variant	NTNG2	GRCh38.p7	9:132227061	GAGCCCACATGGCTA[C/T]AATCTTCCCTGCCCG	84628
rs560588073	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221503	AGGTGCCATGTGTGT[G/T]CCAGCCTTGCCAGCC	84628
rs560596302	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132175536	GCTCCTTCCTAGAGG[A/G]GCCGGGCCATGAGGA	84628
rs560607427	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203512	TTCCAGATCTTCTGC[A/G]GTTACAAAGGAAGGT	84628
rs560624826	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184585	CCTGAAAGCTCCGCG[A/G]GGTGGAGGGGGCATC	84628
rs560657370	snp	A/G	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132227076	TAATCTTCCCTGCCC[A/G]TCAATCCCAGGAGCT	84628
rs560661335	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132178866	GAGACTGAGGCAGAA[G/T]AATTTCTTGAACCTG	84628
rs560672308	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237000	GGAAGTTTGGAGAGG[C/T]GGTGGGGAGAGCAAG	84628
rs560692726	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213450	CACCCACCGGCTGGG[A/G]AGGAGAAACCTCTTG	84628
rs560694318	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244089	TGTAAGCAGGACTGA[C/T]GGGTGGGCTTCCAGA	84628
rs560717158	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132208634	TCATGGAGGACTCCC[A/G]GGCATCTGGCTTTGA	84628
rs560787740	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203029	TTCCTCTGGTTAGAC[A/G]GTGGGAGAGGGAAGT	84628
rs560820895	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132188146	TTCCTTGCCTTCCCC[C/G]ACGATTGCTTCCCCC	84628
rs560857582	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160931	AGAGCCCAGGGCTGC[C/T]GGATATGATATTGTG	84628
rs560863011	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219890	ATTACTGGGCAACTC[A/T]AAGTTCACCTTTTGT	84628
rs560906339	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177053	GGAGTGCAGTGTTGT[A/G]ATCTTGGCTCACTGC	84628
rs560907337	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241151	GGGCGGTGGACTGGG[A/C]CTAGCAAGACGGGGC	84628
rs560966102	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242366	TCCGCCGCCCAGTTC[C/T]TTTTTTGTCTTTCTC	84628
rs561018212	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132188834	GAAGATTTCCCGAGT[C/T]CCTGAGGAGGGCCGG	84628
rs561047865	snp	A/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132208106	GAGACCCTATCTCAA[A/T]ACCCAGGGCAATATG	84628
rs561076157	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243214	GGTGGCCACCTCCGA[C/T]GGATGTGTCATCTCA	84628
rs561104016	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164889	CTGAGGTGCTCAGGG[A/C]GCTCAGGGCAGCAAG	84628
rs561156370	snp	A/G	7.19537e-05	0.00599764	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230639	GGGCCCCCACTGCAC[A/G]AGCCTCTTTGCATGT	84628
rs561164975	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132237009	GAGAGGCGGTGGGGA[A/G]AGCAAGAGACGGGCG	84628
rs561215595	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132218648	ATTACAGGCGCATGC[C/T]ACCACACCCAGCTAA	84628
rs561244703	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171396	ACTGTAAGTTCTTTT[C/T]TAGTGTGAGGCTTGA	84628
rs561258353	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132212816	GTCCCCTGGTCACTT[A/G]TCACCTCTTACTCAA	84628
rs561265763	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182978	GGTGGTCCCAGTGCA[C/G]AGCCAAGTTTGAGAA	84628
rs561339988	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170488	AGGCAGGAAGGGCGA[C/T]GGGCAAAGGCATCTC	84628
rs561349026	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165831	TTTAAATAACATGCC[C/T]GATCTCCAAATGTGC	84628
rs561376947	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172769	AAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	84628
rs561404113	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132195194	ATAGTACAGAAAGTA[C/T]CTAAAACCCCATGCC	84628
rs561439507	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193080	CCCCCGCCACAATGC[C/T]CCCACCCCATAGAAC	84628
rs561442476	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132194643	AGTCCTACCCTGGCC[C/T]GGGCCTCAGTCCCCC	84628
rs561474981	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219996	CTCTGCATCCTCACC[A/G]GCAGGTGATTATCCG	84628
rs561501167	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181863	ACCTCCAGCCTGGGC[C/G]GCCCGGCCCGGCATC	84628
rs561549512	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229322	TGGCACCGACACCCA[C/T]GGGGCCAAGTGCAAG	84628
rs561555445	snp	G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132170150	CAGGAGGGACCCAGG[G/T]GCGGACGGCCTTTTC	84628
rs561607782	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132170893	GGAAGTCTCTGGAGC[A/G]CTGGGGTGGGGTTGG	84628
rs561609949	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132176425	GCTAGACATTTCATA[C/T]GAATGGAATCAGACA	84628
rs561633669	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199732	GACAGGACAGTCCAA[C/T]GGCTTATGGATTAGA	84628
rs561646976	in-del	-/GA			intron-variant	NTNG2	GRCh38.p7	9:132219589	AAAAAAAAAAAAAAA[-/GA]AAGAAAGAAAGAAAG	84628
rs561650695	snp	A/C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132234551	CCCAACAGGTGCTTC[A/C/G]GGCTCTTTGAACAGA	84628
rs561709979	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201520	GAAGCCAGAGACACA[A/G]GACTGGTGGCAAAGG	84628
rs561727678	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132227255	TGCGTGCATGCACCC[A/C]CACACACACACCTTG	84628
rs561769677	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233178	GCTGAGCCTGTGGTG[A/G]GCAGACAGAAGCAAA	84628
rs561814980	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229966	GTCAGGCCTCGCCCA[A/C]TCTCGGCTATATTTC	84628
rs561851096	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188168	GCTTCCCCCGTGCTC[C/G]AGTCCTGGCCCTCTA	84628
rs561856391	in-del	-/A	0.0036615	0.0426303	intron-variant	NTNG2	GRCh38.p7	9:132234122	AACCTCCGCCCCCCC[-/A]GGTTCAAGCAATTCT	84628
rs561881126	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132174779	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGCGC	84628
rs561962796	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211561	CAGCCACCCCAAAGG[C/G]TGGGTCTCTCGGGCT	84628
rs562048042	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211059	CCCTGCTCACAGACG[C/T]GGACCCACAGGGTGA	84628
rs562062481	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132163959	AGGTGAAGATAAATT[C/T]TCCACGGAGAAAACG	84628
rs562072125	snp	A/C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186651	GCCCTCAGGTCCTCC[A/C/G]AAAGGATCTCAGGGT	84628
rs562101526	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223011	CCCAGCTACTCGGGA[A/G]GCTGAGGAGGGAGGA	84628
rs562101541	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216269	AGCACCTACTGTGTG[C/T]CAGGCAGTGTGTTAG	84628
rs562132398	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132216700	GGTTTTCTGGTGAGA[C/T]TGATGGTTCCTGAGG	84628
rs562178941	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203626	AAACAAAATACCCCT[G/T]CAGCCCAGGGCAGCT	84628
rs562202102	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228296	GACAGGCCTTTGAAG[A/G]GGTGACTTGGCAGGC	84628
rs562220161	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132198784	CGTTACCTGGTTCCC[C/T]GGGGGTTACCTGGTA	84628
rs562253955	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180072	CATCCTTCTGTCCCA[A/G]GGCAGTTTGTCTTGG	84628
rs562274212	snp	A/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132186008	TAGCCTCACCCGGCC[A/T]CCCTCTCTCCTTTTT	84628
rs562287704	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132238661	ATGCATTCATCTACC[C/T]GAGGATACCACGGCG	84628
rs562292893	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132232914	AGGGGCAAATGCTGA[G/T]AGAAAGACCTCCTCC	84628
rs562293078	snp	C/T	0.00358779	0.0422022	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162218	CCCAGGTCTCCGCGC[C/T]GGGAAGCCGCTCCGA	84628
rs562294972	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161212	ACCCACCCACCCCGG[G/T]ACCCACTGCTTGGGG	84628
rs562362131	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132191875	CGCGCCCGGCCATTA[C/T]CGCATCTTTCTAGAG	84628
rs562378642	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221445	CAGTACCACCCACAG[A/T]GACCTGCAAAAGTCA	84628
rs562390409	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132209405	AGTCCTGAGCTCCGC[A/G]GTGACGATGACGCCC	84628
rs562405097	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132193281	ATGATAATAATAATA[A/G]GTATAATTGAGTGAG	84628
rs562437346	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173839	GGCCACACCATGCTG[A/C]GGATGAGATGGATGG	84628
rs562450216	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132215483	TACTCGGGAGGCTGA[G/T]GCAGGATAATTGCTT	84628
rs562466553	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132208303	ATGTGGCTGTGGTGG[G/T]TGAGTAAGATTCCAA	84628
rs562478904	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167897	GTATAAAGCAGGAGC[A/G]TCAGGGGAGGGCTCT	84628
rs562500647	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184433	CATTAACCGAAGAAG[C/T]CACTGGGGAAAACTG	84628
rs562552567	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132204363	CTTCCATAAACGTCC[C/T]GTCCCTATTGATCGC	84628
rs562586836	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196809	GTGAAGGGCTCAGTC[A/G]CACCACACTGCCCCC	84628
rs562591810	snp	C/T	0.000186676	0.00965937	synonymous-codon	NTNG2	GRCh38.p7	9:132198409	GGTGCGGGACCGCTT[C/T]GCCATCTTTGCCGGC	84628
rs562738485	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172111	CCCCATGAACTCTCC[A/G]GGCGCTCCAGCCTTG	84628
rs562771133	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214709	CCACACGGGTGAGCC[A/G]GGTAGCAGGTGGGCC	84628
rs562801870	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132231892	GCAGCCCTGGGCAGA[A/G]AGCAGGGGCTTGGCT	84628
rs562802990	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179339	TGAGCTCCCGCCTAT[A/G]TGTCACTACTGGTGA	84628
rs562807693	snp	A/G	0.00438332	0.0466095	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208866	AGCCCGTCTCTCCAA[A/G]AACTCCCGTCCCGAG	84628
rs562825059	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202230	AGCTCCAAGGGGGAC[C/T]CCAATGGCAGGCAGC	84628
rs562845530	snp	C/G/T	0.00159649	0.0282165	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228849	AGGCATGAGCCACCA[C/G/T]GTCTGGCCATGTCTG	84628
rs562861414	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190442	AGATTTCATCCCAGC[A/G]CAGGCTTGGGTGCAA	84628
rs562884982	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236913	CGGCTGGAGCAGGAA[G/T]AGTGTTTCAGAAAGG	84628
rs562887842	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176219	GTGTCTAACATAAAA[C/T]TTGCCTTTTAAACTA	84628
rs562904534	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182442	CTCAGCCTAGAGGAG[A/G]GGCACTGGAAGGAGG	84628
rs562924129	snp	G/T	0.000798403	0.0199641	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231441	CTCCACCAGGGCTCT[G/T]TGGGGCCCCACATCC	84628
rs562946384	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172787	CAGGCTGGAGTGCAG[C/T]GGCGCAATCTCGGCT	84628
rs562981593	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132189931	TGGGATTACAGGCGT[C/G]AGCAACTGTGCCCAG	84628
rs563019216	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183842	TTTGGTTAGTTGGTT[C/G]GTTAATTACTCGATT	84628
rs563039001	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176625	GCTTCTGCTTTCTGG[C/G]TATTAGGAGTGATAC	84628
rs563068249	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171886	CAGCCTCCCTCCTCT[C/T]GCCGTCACAACCCTC	84628
rs563091026	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243450	GAAGCTCCTAGATTC[A/G]GGGCTCATCCCCTGG	84628
rs563096259	snp	A/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132189147	AGTGGCACAGTTACG[A/G]CTCACTACAGCCTCG	84628
rs563110019	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166582	TTAGGAGGACGTGAA[A/G]TTATGGGCAACTTTC	84628
rs563131800	snp	A/G	0.0115144	0.0749975	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242308	GCGCCTTGGGACTCC[A/G]GTCCCCGCGCCTGCG	84628
rs563307055	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225709	TCCATTTGTTTGCGT[G/T]TTTGATTTTACAGGA	84628
rs563320370	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165761	CTCTGACCCCCAAGC[C/T]GGGGCACTTCTGCTG	84628
rs563324363	snp	A/C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132235184	CCGGTCCCTGGATTG[A/C/T]GGCTGGACAGGAAGG	84628
rs563345575	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132219825	CAACATTCATGTACA[C/T]ATTTTGTGTGGACAT	84628
rs563379125	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194786	CAATGAACCGAGGGT[A/C]AGCCCTGCCACCGAG	84628
rs563380288	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183013	CGATTGAAACCTCTC[C/T]CAGGCCTGCCCTGGA	84628
rs563406457	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213415	TTGAGGCCGTCCATC[A/G]TCCATCCATTGGCCA	84628
rs563482184	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204397	GTAACTGGAGATGGA[C/T]GGACACCGGACTAGA	84628
rs563515425	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213091	TGGGAAGGCAGATCA[C/T]CTGAGGTCGGGAGCT	84628
rs563517515	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201678	GCTCCGCTGTGGCCC[A/T]CTAACAAGAACAGCA	84628
rs563522542	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235739	GGGGGGGCAAGGCCT[A/G]TGATGGGCCTGAGAC	84628
rs563538104	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229287	TCACCCTGCCCCTAC[C/T]GTGACCCCTCCTCAG	84628
rs563554454	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223700	GCCGCACACCCCAGG[C/T]GGGACGGGTGGGCCC	84628
rs563621233	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132188763	CCTGGCATCATTCCT[A/G]TGACAACCCTGTGAA	84628
rs563647938	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175948	AGTGCAGACAGAGGG[C/G]TCCTAGATGTATACC	84628
rs563759145	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132237017	GTGGGGAGAGCAAGA[C/G]ACGGGCGTGGTGTGC	84628
rs563780648	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199690	ATGTGGCCCAAGACC[C/T]GCAGGCAAACATGGA	84628
rs563799050	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228778	GCCCAGGCTGGTCTC[A/C/G]AGCTCCTGAGCTCTA	84628
rs563817382	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200255	GTGCTGGGGCAGTCC[A/G]GGCCAGGAGCCTGGC	84628
rs563849101	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164833	GATGAATGAGTCCCA[C/T]GCCTGGAGCCCTGGG	84628
rs563874060	in-del	-/AAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132178801	CAAAAAAAAAAAAAA[-/AAAAAA]TTAGCTGGGTGTGGT	84628
rs563915287	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239798	TCCTCATTCATCAAA[C/T]TGGGAGGCAGATCAG	84628
rs563948485	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132233878	GTAAATTACACCTCA[A/G]TCAAGCTGTTTCAGA	84628
rs564004633	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205153	GACTTGAACAGATAC[C/T]TGTACACCCATGTTT	84628
rs564043291	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132205577	TAATGCCACCAGACT[A/G]TACACTTAACAATGG	84628
rs564055881	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162884	GCGTGGAGTCGAACC[C/T]GGAACTGAGCGGCGC	84628
rs564098694	snp	A/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132185169	AAACCACTGCTGGGG[A/T]CCAGGCTTCACTCTC	84628
rs564109630	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240372	CCTCCACCCCGAGAG[C/T]CAGCACTGAGCTGCA	84628
rs564111166	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132165958	TACGTCTCTATTCTC[C/T]CCCTCTTTAATTTGT	84628
rs564121619	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232552	CACCTGGACTCACCT[A/G]GGGAGTATCCCTGCA	84628
rs564123286	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201639	GATTCCCTCAGAATT[C/T]CGTGACTGCCATGTT	84628
rs564207043	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203605	TGTTTAAACTCTGTG[C/T]AAGGAAAACAAAATA	84628
rs564228435	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193682	CAATTCGTCTCTACC[C/G]CTCTGAGCCATTCCT	84628
rs564240069	snp	A/C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132179513	CCGGGTAGGATGGTG[A/C/G]CTGGAATGCTGGCGA	84628
rs564323722	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159663	GTATTGGTGAGGTGG[A/G]GGCTGGCAGGGAGGC	84628
rs564336510	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216651	TGGATGAGCTGAAAA[A/G]TGCTGTGTCGGGGGA	84628
rs564341403	in-del	-/GTGCCGTCC			intron-variant	NTNG2	GRCh38.p7	9:132236830	GGCAGTGGAAGGCAG[-/GTGCCGTCC]GTGTTCCTGGCTTGA	84628
rs564356600	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160565	CAAGATTCCAAATAT[C/T]ATTCAGCAGTATAAC	84628
rs564394685	in-del	-/TTTTGTTTTG	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132225260	TTTTGTTTTGTTTGT[-/TTTTGTTTTG]TTTTGTTTTGTTTTT	84628
rs564419712	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132161818	GCGCCGCGCCGGGGG[A/G]ATGCCCCGGCTCCCC	84628
rs564451023	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227625	GAGCTTCCGTTATCC[A/C]TTTTTACAGATGTGT	84628
rs564466679	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191672	CACCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	84628
rs564487047	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228150	AGGCCTGGGCAGTGG[A/C]CTCCTGCACCCCATC	84628
rs564524982	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222537	AAAATCACACAGACT[G/T]CAGCGGTGGCTAGTG	84628
rs564587950	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182043	CCCCCAGCACACCCC[A/G]GCAGCCCAGAGAAGG	84628
rs564665717	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132232815	ATCCTTCCCCCTTGG[G/T]GGGTGGCATTTCTAA	84628
rs564709656	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204304	GGCCTCCCCCAACCT[C/G]TTTTTTCCTCAACAC	84628
rs564715251	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187918	CAGCCCACTCCTGCC[C/T]GGTCATTTTGTGAAC	84628
rs564717403	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211087	TGAGCGGAGGCCTCC[A/G]CAGCAGCCCGGGGTT	84628
rs564751379	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226439	CAGCCCATGGCCAAG[A/T]CTCTGTCTACACCAG	84628
rs564758414	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214651	AGTGCGCCCCATGTC[A/T]GGCCGTGAGAGAAGT	84628
rs564780051	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132226298	TGAATAATACACCTG[G/T]GAATGAACTGACGGG	84628
rs564790182	snp	C/T	1.76874e-05	0.00297378	synonymous-codon	NTNG2	GRCh38.p7	9:132226906	GGGCAGCCTGCAGTG[C/T]GAGTGCGAGCACAAC	84628
rs564792614	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132209937	GGAGGGACGCTGGGG[A/G]CAGGAGCCGAGGAAG	84628
rs564870534	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172892	CTGCCACCACGCCAG[A/G]CTAATTTTTTGTATT	84628
rs564874300	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212456	AAAGGGCTTCGCACA[A/G]AAGCCCAAATTTGAT	84628
rs564878119	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132186132	CACACTCGAAGGAGG[A/G]AGCAGTGGGGTTTCA	84628
rs564890972	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132214013	GTTCAGAGCCATTGC[C/T]GTGAACACTCTGAAA	84628
rs564977699	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203719	CAGCTGCATTCGATG[G/T]GCCCAAGGCAGGGCC	84628
rs565017643	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244726	GAGTCCACCTCTGTC[C/T]AGAACAGGACTGCCC	84628
rs565092161	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132214876	AAATTCAAAAAAAAT[-/T]TTTTTTTTTTTTAGA	84628
rs565137984	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220741	GCGTGAGCCACCGCA[C/G]CTGGCTCCCTACGTT	84628
rs565159190	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243859	GCCCCTCCTGGCCTC[C/T]TCTCTCTGCTCCCAC	84628
rs565162652	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212904	CTCCCCACACTGCTT[C/G]CCTGAGCCAAGGACA	84628
rs565201409	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213308	GCCTCCAGCCTGGGC[A/G]ATGACAGAGTAAGAC	84628
rs565209073	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132202777	GGTTCCCCAGCCCCA[C/T]CACTGAGAGCTTTGG	84628
rs565218703	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177876	TGGCCAGGCTGATCT[C/T]GAACTCCTGGACTCA	84628
rs565258510	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166471	CATGCAGGATCCCTG[C/T]GGATTTTCTCCTTAT	84628
rs565275787	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236844	GGTGCCGTCCGTGTT[C/T]CTGGCTTGACAGCAC	84628
rs565282868	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132236215	CAGCACATTCCAGGC[C/T]GCAGGGCCAGCCGGG	84628
rs565341023	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176940	TGATTTGCATTTCCC[C/T]GATAGCTAATGATGT	84628
rs565356671	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195984	CTGTGTTGCCTGGGC[C/T]GATCTCAAACTCCTG	84628
rs565392864	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211779	GCCTTGCCATAGCTA[C/T]CATAGCTATGCACGT	84628
rs565401838	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132189337	TAAGGAATGAAGACC[C/T]AAAACATTGGTGAAC	84628
rs565403545	in-del	-/TGAA	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132226271	TCGCCTATAAATATT[-/TGAA]TGAATGGATGAATAA	84628
rs565420298	snp	C/G/T			intron-variant	NTNG2	GRCh38.p7	9:132191876	GCGCCCGGCCATTAC[C/G/T]GCATCTTTCTAGAGA	84628
rs565442387	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201783	TGTTTAATCAATAGC[C/T]GTTTAATTCCCCAAT	84628
rs565478100	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132171487	TCAAATTTCAGCCAT[A/G]TTGGAGTCTCCAGCA	84628
rs565499361	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132175120	GAGACGCAGGGAAGG[A/G]GGCCAGGTGATTCGA	84628
rs565515140	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132192872	CGCTCCACAGCAGGC[A/G]AGGGGCCTGTAAACA	84628
rs565566871	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205035	TGGTGGGAACAAAAA[C/T]GGTGCAGCCACAGGG	84628
rs565625460	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132187030	GGCGGTGAGGAGAGC[A/C]GCTCTGAGCAACCAA	84628
rs565630197	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181430	AGTTCAAGCAATCCT[C/T]CTTCCTCAGCCTCCC	84628
rs565661457	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187451	AATCTGGAAAGGGAA[A/G]GAGAGAGACACCTGC	84628
rs565703222	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169144	CCTCTCCTGGGCAGA[C/T]AGGTGGGGAAGGCAG	84628
rs565739381	snp	G/T	0.00119737	0.0244387	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162214	CCCTCCCAGGTCTCC[G/T]CGCCGGGAAGCCGCT	84628
rs565755557	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132201496	GCTGGGAAAGTCCAG[C/G]CATGCTGAGAAGCCA	84628
rs565814014	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170615	TCTCCCGCCAGCCAC[C/T]TGTGGTCCCCGTGAG	84628
rs565858227	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180918	GCACACACACACACA[C/T]ATAAGGTTGCAAACA	84628
rs565874067	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223291	GGCCGCTGTTTCCCC[A/T]CCCAGATCCTTGCTC	84628
rs565885209	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229075	GACTCCTGAGCTGGC[C/T]CCACCTCCTGCTTCC	84628
rs565966926	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132205302	GGAGAACCTGACACA[C/T]GCTGCGACACAGATG	84628
rs566005339	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132199115	CTGAGCTTTTCCACG[A/G]AAGAAGGTGCACATG	84628
rs566059863	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168484	AAGGTAGCTTCTTAC[G/T]CAGGCTTGTCAGTGG	84628
rs566062994	in-del	-/ATTG	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132164159	TGCCAGCAACGCCCA[-/ATTG]ATTGACTAGTTGTAA	84628
rs566096316	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232239	CACCTGGCCCCCAGG[G/T]CCTCTCTGTCCTTAG	84628
rs566122899	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222038	CAGGGGGGTGTTAGA[C/T]AGGAATTCAGAAGTT	84628
rs566125910	in-del	-/A	0.0158469	0.0875917	intron-variant	NTNG2	GRCh38.p7	9:132182255	GGGAAGGAGTGGGGG[-/A]AAAAATTGCACCCAA	84628
rs566132926	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232977	GCAGCACACCCCACC[G/T]CTTTCTACATCCTTC	84628
rs566166295	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199810	TGCAGGGTGTGGACA[A/C]CCCAGGCCTGCTGTG	84628
rs566213399	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240114	TGCCCAGCCAGGCCC[C/T]TTGGGACACCATCAC	84628
rs566218469	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244806	ACAGCAGCGCTGGCC[A/G]CAGTCGGTAAACAGC	84628
rs566231606	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132174014	TGCTACGGATGAGAC[A/G]GACGGATGGACGGAC	84628
rs566256150	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132216739	CAGAGAGCGATCGCT[G/T]GGGAAAATTGATCCC	84628
rs566277477	snp	C/T	0.00358779	0.0422022	intron-variant	NTNG2	GRCh38.p7	9:132184886	AAGATCGTACCAGTG[C/T]ACTCCAGCCTGGACA	84628
rs566321216	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208455	GAAATCTGAGTTGGG[G/T]GTGGCGGTGCTGGAG	84628
rs566327911	snp	A/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132216377	AATCTGGCTGCTGAC[A/T]CAGCCTCTCTCTCTC	84628
rs566352948	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180273	GAAGAAGAGACCAAT[A/G]AGAGATGAGCCCACG	84628
rs566359951	snp	C/T	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132190294	ATGTCCTGGGCTTCA[C/T]TGGGCTCAAGGAAAT	84628
rs566401500	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132208240	CGGCATTTGTGGCAG[A/G]GGGACAGCAGGCAGG	84628
rs566403582	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237593	GCCGCTGGAAAAAGA[C/T]GGTGCAGGATAGAGG	84628
rs566488788	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227784	TGAGGACCACCCACC[C/T]GGGCGCGCTAGCGTA	84628
rs566522270	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132191000	CAAGATTCCTCAAGG[C/T]TGGGTCCCGTGGAGT	84628
rs566558960	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184822	AGCTACTTGGGAGGC[C/T]GAGGTAGGAGAATCA	84628
rs566579177	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214173	TGACATCACTCTTTC[C/G]GGCAGCCAGGAGTTG	84628
rs566612842	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203980	GTGGGAGATGATGAA[A/G]GGAGGTCCTTTGCAC	84628
rs566632182	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244355	TTTATTTATCTACTT[A/C]TTTTTATAGAGTTGA	84628
rs566638905	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132167268	ATGTGACATTGTTCT[C/T]TGGGGTAGGGGCATT	84628
rs566639051	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NTNG2	GRCh38.p7	9:132244914	AGCAGGGCCCAGCCC[C/T]AGTGGCCAGCCCTGG	84628
rs566684330	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203338	GAGAGAGATCCTGTC[G/T]CTAAAAAAATAATAA	84628
rs566734508	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132226622	AGCAGAGAGGAGAGC[C/T]GCGCAGTGACTGCAG	84628
rs566769400	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220932	TTTGGTTTCACTTAG[A/G]CAGTATTTTTGTGAT	84628
rs566772735	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196213	GTTTTTGTTTGATAC[A/G]GAGTTTCACTCTTGT	84628
rs566800960	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189403	TCATGGAGAAGTACG[A/T]TTGGCTTAAAAAAAA	84628
rs566839711	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178096	AGACTCCAAAACTGA[A/G]TGAAGTCAAGGCTCA	84628
rs566856061	snp	C/T	0.00257443	0.0357853	synonymous-codon	NTNG2	GRCh38.p7	9:132198469	CACGCGGCTGGAGAG[C/T]GCCAAGGGCCTCAAG	84628
rs566923435	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165962	TCTCTATTCTCCCCC[C/T]CTTTAATTTGTTGCA	84628
rs567020317	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238499	TAAAGTGGCACTCAC[C/T]CTTAGCATCCTGCAA	84628
rs567059788	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166649	TGAATTTTCCGTGTC[A/G]GCCTTTTGGAAACAA	84628
rs567073226	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231149	TCCCAGGGGAGTCGG[A/C]CCAGGGAGGGGCATC	84628
rs567085926	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132182346	CTGTCTGCCAAGGGA[C/G]GGCTCCAGGCCTGTC	84628
rs567106727	snp	A/G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132192931	TCTGCTTCCCGGGCC[A/G/T]GGGCGGGGGCCGGAG	84628
rs567174911	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213731	CACTCTTCACCCAAA[G/T]ATAAATGCGCTATCT	84628
rs567196758	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226151	TTCTATAAAAAGAAG[A/C]TTCCCCTCATCAACT	84628
rs567212532	snp	G/T	0.000399281	0.0141238	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231486	CTCCCGGACCCAGGG[G/T]GCCCCTGGCTGGGAA	84628
rs567221952	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132207651	TCAACATATCTTTTC[A/G]GGAGACACGATTTGG	84628
rs567248768	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171134	CTGAGCAGGAGCCAG[C/T]GGAAGGTTCCAGAGA	84628
rs567261437	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213097	GGCAGATCACCTGAG[A/G]TCGGGAGCTCAAGAC	84628
rs567289892	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234795	CCTGGCGGCCTCATC[C/T]TCCCACTGAACATCA	84628
rs567290489	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207355	GAATCTGTCCCATAC[C/T]CTCCGCCCTCCGCTC	84628
rs567295435	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243562	CAGCCTCCTGTCCAC[C/T]TATGTTTATTTCAGA	84628
rs567389490	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235082	CACTGGTTCATGCTG[A/G]GGTCCCTGGTGAAAA	84628
rs567397982	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132235988	AGGTTCCATGTGGCA[C/T]CCCCACGCCAAGCCC	84628
rs567407572	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132182077	GGCCCGGAGGAGTGA[C/T]GGTGTTCCCCACCCC	84628
rs567432460	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132224431	AGAATGGTTTCACCG[C/T]CCTAAAAATCCCTGT	84628
rs567437832	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182577	CTTGGGTGGACGCTG[C/T]GCCTCATCAGCCCTG	84628
rs567484584	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132218461	AGACTTCCTTTGAGG[A/C]ACAATGTGATAGCGT	84628
rs567520959	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212563	GAAAAGCCAGGCTGC[G/T]CCAGGCGACCAACCC	84628
rs567555325	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211728	CCAGCCCCTCGGTCC[A/C]CTTCTCCAGCCTTGG	84628
rs567558448	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229583	CACAGAGCCTCACTT[A/G]GTCACCACCCAGTCC	84628
rs567576041	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194512	GCTGGGAACCCCCCC[A/G]CCCCATGTCCCTCTG	84628
rs567600331	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201395	AAACACTCTTCAGGC[A/G]GCAGCTTGGCTTGTC	84628
rs567663838	snp	A/C	1.75394e-05	0.00296132	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240869	AGAAGACGGCGCCCA[A/C]ACGTAGCCCTGACCG	84628
rs567701263	snp	G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132222766	CAGAAACTCACTGCC[G/T]TCTCCACTCTGGCCT	84628
rs567739428	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132223271	CCAGGGCTGGTGGAC[A/G]CAGGGGCCGCTGTTT	84628
rs567748416	snp	A/G	0	0	intron-variant	NTNG2	GRCh38.p7	9:132194821	CCCAGGCAGCCAGGG[A/G]ACCTGTCCTTCACCC	84628
rs567757212	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132211348	GTCAGGATTTGGTTT[C/T]GGGACATGACTGGCC	84628
rs567759158	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132163633	TGGGCTGAGTATCCC[C/T]CCTAGCCCCGGGAGC	84628
rs567775938	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132188362	GGAACCCGAGTCTGC[A/G]GGAGCACAGTGCGGC	84628
rs567776591	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216995	TTCTTTGTCCCCATG[A/G]AATGGACGCGAAGCC	84628
rs567791294	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229970	GGCCTCGCCCACTCT[C/T]GGCTATATTTCTCCC	84628
rs567800113	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205882	AGAGACTCCATCTCA[A/G]AAGAAAAAAACATGG	84628
rs567822654	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188865	GGGCTGGGGCTGGAG[C/T]GGGGACAGGATCAGA	84628
rs567827408	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175540	CTTCCTAGAGGGGCC[A/G]GGCCATGAGGAACAG	84628
rs567861796	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170485	AGGAGGCAGGAAGGG[C/T]GACGGGCAAAGGCAT	84628
rs567919219	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132180388	CTGGGGGATCAAGAG[A/G]TGGCCAAAAGCAGGT	84628
rs567920441	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206404	GGGCGTGGTGGCTCA[A/C]GCCTGTAATCCCAAC	84628
rs567962092	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132199020	CCTAGCACCTGGGAC[A/G]TTACCTGGTTCTCAG	84628
rs567971446	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132200648	TTTGTTTCACTTTGA[C/T]GGTGTGTGTGGATTC	84628
rs568000479	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132177234	TCAAACGATCTGCCC[G/T]CCTGGGCCTCCCGAA	84628
rs568007969	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132164230	GTTTTTTAAATTTAT[G/T]TATTTTCCAGGGAAT	84628
rs568081516	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173977	ATGGACAGACGAACA[A/G]ACAGGCAGGCAGGTC	84628
rs568110605	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132196816	GCTCAGTCGCACCAC[A/G]CTGCCCCCACCTCTG	84628
rs568140872	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132180796	AGAAAACCCTGGAGC[A/G]GGAGCTTCTCACTTT	84628
rs568152078	in-del	-/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132225949	CCTCTGTCTTTCCTG[-/T]TGCGCTCACAGCTGG	84628
rs568166686	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233436	AAGTTGGGAATTAAA[C/G]AGGAAAAGTCAGAGG	84628
rs568187244	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132193784	AGCACACGAGACCCA[G/T]GTGGCTTAAACAACA	84628
rs568192596	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174962	TTATCCTTTTTAATT[A/C]TAGAATTTAGCTTGA	84628
rs568223689	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132162144	CTCGGCCCGCGCCCC[C/T]ACCCAGCGCCAGCCC	84628
rs568230714	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132239391	AGACTGTGGGAATTC[G/T]AACTCCAGGGCCCTC	84628
rs568306061	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228449	GAGGTCTCTCTTTAG[A/T]GGCCGTCACTCTCTC	84628
rs568364404	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168389	TTGTGGTGGGGCTGA[C/G]CCGGTGCCCCCACCT	84628
rs568399753	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239438	TAAGGACAGAAAGCT[C/G]CAGAAACTGCTCTAT	84628
rs568407831	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179142	GACTGGAGCCATGAG[C/G]ACAGGGGCCCTCCCC	84628
rs568434755	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204538	CATCTCTTTCTCAGC[G/T]GCTCTACAGGAAAAA	84628
rs568463296	in-del	-/CGGCGGCGG	0.030665	0.119967	utr-variant-5-prime, upstream-variant-2KB, intron-variant	NTNG2	GRCh38.p7	9:132162064	CTGGCCCCGATCTGA[-/CGGCGGCGG]CGGCGGCGGCGGCGG	84628
rs568464473	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215909	AATAATAATAGCTGA[C/T]GTTTCCGGAGGGCAT	84628
rs568501738	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160921	TGGGGATCAGAGAGC[C/T]CAGGGCTGCCGGATA	84628
rs568515821	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132184721	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	84628
rs568544792	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227239	TGCACAGAAACACAC[A/G]TGCGTGCATGCACCC	84628
rs568580619	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168774	CAACCTCTGTCTCTC[A/G]TATTAGAGTCTCGAC	84628
rs568691316	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221601	GGAGGCACTGTGCTT[C/G]TTCTGGGGCTCAGCC	84628
rs568710745	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220811	TTTTGAGTTAATTTT[C/T]ATATGTGATGTGAAG	84628
rs568710755	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132178682	TGGTGGCTCACACCT[A/G]TAAATCCTAGCACTC	84628
rs568728186	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132221985	TGCGGAGCACAGCCC[C/T]GGTTCCGTACAGCTG	84628
rs568730639	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185293	AGCAAGAAAGCCCAG[G/T]GCAGCTCTCAGAGAA	84628
rs568731996	snp	C/G/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132215082	TTGTAGAGATTGGGG[C/G/T]GGGGGGTCTCACTTT	84628
rs568842626	snp	C/T	0.000399281	0.0141238	intron-variant, missense	NTNG2	GRCh38.p7	9:132231694	GCCCTGTGGCCACTG[C/T]GGCCACCACAGCCAT	84628
rs568844554	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159792	TGTTTAGATGAACTA[C/T]AAGTAAGAAGCAGCT	84628
rs568856335	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244283	GTGAAGGGTGGAGCC[A/G]GGGGTGGAAGTTGCA	84628
rs568876002	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132190913	TAGCCACACTGCCTG[A/T]CCTTTCAGGTGACTT	84628
rs568904292	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232176	GCCTTATCTCCCAAT[C/G]GTGCTTCTGCCTCCG	84628
rs568919780	snp	C/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132203798	GCTCTGCCCACTCCA[C/G]ACCTGGGAGTCAGAG	84628
rs568967573	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220123	CATCTGCTTCTTGGC[C/T]ATTTGTATGCCTTCT	84628
rs568978935	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217029	ACTGAGAGAGACGCA[A/G]GCAGCAGGTGGCTGT	84628
rs569030900	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178039	CTGCACTGTAGAAAC[A/G]ATTACTCTCCTGTTG	84628
rs569033588	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213579	CTTGTTGCTTCAGCC[C/T]CCTCCTTCATCCTGC	84628
rs569091482	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167179	TTGACCAGGTCTGGA[A/C]CAGACCTGGACCAGG	84628
rs569112153	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189378	TATGCTAGGTTTAAT[A/G]GAGAAATAGTCATGG	84628
rs569140530	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231063	CTAGCCTAACCATGG[G/T]GGCAGCCTCCCTCTG	84628
rs569170498	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132172972	CTGACCTCGTGATCC[A/G]CCCACCTCAGCCTCC	84628
rs569180949	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132203201	ACGTGGAAGCCAGGC[A/C]TGGTGGTGTGCGCCT	84628
rs569187973	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182791	TGACCCCACCAGGAG[C/T]GGAGCGGGCAGGGAC	84628
rs569228555	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132196029	TCCTGCCTCGGCCTC[C/T]CGGAGTGTTGGAATT	84628
rs569233600	in-del	-/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132210768	CCTTGTTCTGCCCCT[-/G]GGCTGGGCTGCCTCC	84628
rs569244762	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183147	GCTGCAGGTGCTCCA[C/T]CCTCCTTCTGGCTTC	84628
rs569268385	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132176302	ACTTAGTCCCAACAC[A/G]TTTCCATCGCCCCAA	84628
rs569326483	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165946	CTTTTGTTCTTATAC[A/G]TCTCTATTCTCCCCC	84628
rs569428987	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242934	GGTTTCCCTACTGGG[A/G]CCACCATTTCCCTGG	84628
rs569524369	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202844	TCTTTGCAAAGCTCC[C/T]CAAGTGAGCTGGAAA	84628
rs569571148	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132186259	TCCATTCTGTCAGTC[A/G]CCTGTGGGGTGCCCC	84628
rs569580503	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230399	GGATAATCCACCCCC[A/G]TCCCCACACCCTGCA	84628
rs569583803	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214370	CTGCAGCGCAGGGCA[C/T]GCTCCTGCCTGGCAC	84628
rs569668233	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132218380	GCTAATGTTCTAATT[C/T]GGGTGGCACTCTCAG	84628
rs569702620	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206856	CCACTGAGAAGTGCC[A/G]GTGTTGGGAAGGGGC	84628
rs569728581	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171070	ATGGAGCTGGGAGCC[A/G]AGATTCCCAGATGCG	84628
rs569730244	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240761	GAAGTCCCCACCTGC[C/G]GTCCAGCCGCGGGCT	84628
rs569773267	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229909	ACCAGGATCATAGGC[C/T]TCCCCCATCCCCTGG	84628
rs569808131	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193701	TGAGCCATTCCTCCC[A/G]GCCTGTTCCCTCTTT	84628
rs569813308	snp	G/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132217848	CAGTGGGGCCCAGGG[G/T]ATGGGGTTACCATCT	84628
rs569860971	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183659	AGGGAGCAAATTGCC[C/T]GAGTCACCAGAAGTG	84628
rs569904434	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240210	CGGTCTGAATTCTGG[C/T]GGCAGCCTTCAGATA	84628
rs569912303	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223208	AGACCCCAAGGAGGA[A/G]GGCAGCCCTGGTTAC	84628
rs569927649	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132224384	TTTTGCCATATGCAT[A/G]ATGCCACATATCTAC	84628
rs569959594	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234147	AATTCTCCTGCCTCA[C/G]CCTCCCGAGTAGCTG	84628
rs570101014	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132227800	GGGCGCGCTAGCGTA[A/G]TCCACACTGTCTCCA	84628
rs570132999	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132200581	GGTGATGCCTGTGCC[A/G]TGAGGCTGGGCAGGC	84628
rs570135832	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228379	ACAGCCCACTCCAGC[C/T]GCTGCCTCCTCCCAG	84628
rs570136193	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132222218	GATGTCAGGGGATTT[A/G]GAGAGCATCATATGC	84628
rs570140244	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193960	CCCAGCGTCTCATCC[A/G]GCAGCCAAACTTCTT	84628
rs570145680	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216460	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTCCCATG	84628
rs570173618	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222695	TGCCCCCTCTCCCAC[A/G]GCCCACCCAGGACCT	84628
rs570254587	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205803	GGAGAATCACTTGAA[C/T]CAGGGAAGTGGAGGT	84628
rs570303623	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132209570	GCCACCTGTGTCCAT[C/G]CTGCGGCGGGTCCAA	84628
rs570343681	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204509	CCACCCTATTCCTGT[A/C]CCCACCCTCCCTGCA	84628
rs570364738	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132169880	CCCCAGCCTTGGGGA[C/T]GCCACGCCTTGTATT	84628
rs570364828	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132233777	TATTCTGGGCTCACA[C/G]CTCCGTGAGATGGAG	84628
rs570370712	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205697	ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCCATC	84628
rs570414086	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233415	GGAGGCTGGGCAGAT[G/T]GTGCAAAGTTGGGAA	84628
rs570494098	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177951	CGTGAGCCACAGCGC[C/T]TGGCCTCAAATCTAT	84628
rs570564643	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132238697	CGTGAACCCAGGCGT[C/T]GCCCTCCCCCAGTGC	84628
rs570565858	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209002	GCTTATGGCGTGGCC[A/G]CCTGCGTGGCTCGGG	84628
rs570567522	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180999	TCAATCATCTGGCCT[A/G]AGCAGGTTCTGCCTT	84628
rs570581480	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132180305	TGCTCCTGCCCTCCA[C/G]CAAGGCAGGCCATCC	84628
rs570598062	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132237966	GGGAGTGCCCACCAT[C/T]TCTCCTGGGCACAGG	84628
rs570629391	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132195465	AGGCGCCCACCACCA[C/T]GCCTGGCTATTTTTT	84628
rs570630229	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160141	CATCTGAGAGCATGT[A/G]CAGGTAGAGGCACAC	84628
rs570657139	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132197874	CAGAGCAGGTTTCTC[A/G]GTTCGCAGGCAGGGG	84628
rs570662873	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191588	TTTTTCTTTTAGACA[C/G]AGTCTTGCTCTGTCG	84628
rs570666502	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160788	TGACAGTGCTGGCTG[C/T]TCAAGGCTGCAGTGA	84628
rs570676270	snp	A/G	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132199193	AGCCTGTCTGGGCAG[A/G]GCTGGGCTAACTCCT	84628
rs570728373	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132198875	CTTGGGATGTTACCT[A/G]GTACCTGGGACATGA	84628
rs570773248	snp	C/T	1.6755e-05	0.00289435	intron-variant	NTNG2	GRCh38.p7	9:132239289	GAGAGGGCACGGACA[C/T]GGCACAGGGAACTTG	84628
rs570789777	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197128	GGCGCAGTGGCTCAC[A/G]TCTGCAATCCCAGCA	84628
rs570829799	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178217	CCCTCATTTTCTTCT[C/T]CCTCTTTCAGGCTGG	84628
rs570881836	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166675	AACAACAAGTTCCTC[A/G]CTGTTTGCAAAGCTT	84628
rs570888478	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132168000	GTCATTGTGAGGAGT[C/T]TGTGGTTTAATTAAC	84628
rs570920639	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132167053	CTCCCATGTAAGTCC[A/G]CTTACTGCTCTTTTG	84628
rs571029997	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231219	AGGGCGACATGGCGC[C/T]CACAGGTTATCAGTA	84628
rs571030548	in-del	-/TTTT			intron-variant	NTNG2	GRCh38.p7	9:132195497	TTTTTTTTTTTTTTT[-/TTTT]GTATTTTTAGTAGAG	84628
rs571078797	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132226744	TTCTTCCTGGGCAGC[C/T]CAACACCCTCCTGGG	84628
rs571161630	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132183388	CAGCAGCGTGCATGC[A/G]TTAACCCATTGCCCC	84628
rs571168512	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244242	CTTCTTGAGACACTG[A/C]GCATAACAGTGTCAC	84628
rs571173420	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243607	CCGGTCCTGGTTGCT[A/T]ACTGCTGCCACTGCT	84628
rs571201752	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132227083	CCCTGCCCGTCAATC[C/T]CAGGAGCTGTGGATC	84628
rs571256269	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207683	CCACAGCAGGCACCT[A/G]TGACATGCTGGACAC	84628
rs571271298	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229998	CCCCAAGCCGTGTGT[C/T]CTCAGCTGTAGAATC	84628
rs571292677	snp	A/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132202482	CCCTCCCTGCCTCCC[A/G/T]CGGAGCCTGCTCCAC	84628
rs571304089	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132237024	GAGCAAGAGACGGGC[A/G]TGGTGTGCAATGTGA	84628
rs571326803	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132189445	CTGGTGATAAACTGG[C/T]GGGAATTTTGCAAGA	84628
rs571367267	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132220037	TCTGCCTATCCTGGT[A/G]AGTGTGAAGTGGTAT	84628
rs571437308	snp	C/T	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132213139	ACATAGTAAAACCCT[C/T]GTCTCTACTAAAAAT	84628
rs571446896	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132225270	TTTGTTTTTGTTTTG[G/T]TTTGTTTTGTTTTTT	84628
rs571448342	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177105	AATCATTCCTGCCTC[A/C]GCTCCCAAGTAGCTG	84628
rs571486918	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132172115	ATGAACTCTCCGGGC[A/G]CTCCAGCCTTGGCCC	84628
rs571515547	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132235848	GGTTGGAGGGGGGCC[A/G]CAGGAACCAACTGAG	84628
rs571517245	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171680	GCTGGGCTGTTGAAT[A/G]CAGACAGCAGGCAGG	84628
rs571520693	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132207385	CGCTCCTGGTGGGGC[C/T]GGCAGCCTCTGGCGT	84628
rs571532750	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132206820	AAAGCGGGCATGCAC[A/G]ATTCCAGACCACATC	84628
rs571591753	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195380	GTGGCGCGATCTCGG[C/T]TTACTGCAAGCTCCT	84628
rs571605246	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132163720	CCCACACGGCGAGGG[C/T]GCAGCAGGCAACTCC	84628
rs571644195	snp	C/G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132220758	TGGCTCCCTACGTTT[C/G/T]CATCTGAGAGTTTTC	84628
rs571698525	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186684	TCTGTGGGGGCAACC[C/T]GAATTGGTGTAAGAA	84628
rs571712539	in-del	-/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132219223	CTGTCTCAAAACAAA[-/C]AAAAAAAAAGAAAAA	84628
rs571717232	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132188407	CCTTTCCCTTTTGGG[C/T]GAAGGGCACCATTTC	84628
rs571727129	snp	C/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132211392	TCAGTCTTGCCCTTT[C/G]TGTAGTTTTTTGTCC	84628
rs571755278	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182119	GACACAATGGAGTCC[A/G]CTAATCCAGTTACTT	84628
rs571777329	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200676	TTCCAGGTGGGCAAA[G/T]GCAAAGGCAGGTCGT	84628
rs571791973	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182729	CTTTTCCATCTCCCA[A/G]CACTTGGGGCAGTCT	84628
rs571803669	snp	A/G	0.000399281	0.0141238	intron-variant, missense	NTNG2	GRCh38.p7	9:132231476	CAAGTTGTCCCTCCC[A/G]GACCCAGGGGGCCCC	84628
rs571807208	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132217364	CTGTGTCTGGGGGAG[C/G]TGTGGGGTGGCTGCA	84628
rs571873877	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132164973	GAGAATGGAGTTTCA[A/C]GGAAACACAGTTAAC	84628
rs571874395	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201432	CTCGGTTGGGTTAGA[C/T]GGTTCAGCGAAGGAC	84628
rs571896764	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132241810	GCACACCCTGCTTCG[A/C]AGGAGCTCGGAGGTT	84628
rs571911297	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132194877	GGCTGCTGCAGTGGC[A/G]CCTGGTGGGGGCCGC	84628
rs571957561	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186502	GGCTGACGGAGGAGA[C/T]CAGTCATTCAGGGGT	84628
rs572001616	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199524	ATGCTTGTGAACTAT[C/T]ACCAGGCAGGGATGC	84628
rs572069808	in-del	-/C	0.00636936	0.0560724	intron-variant	NTNG2	GRCh38.p7	9:132234114	TCACTGCAACCTCCG[-/C]CCCCCCCAGGTTCAA	84628
rs572076009	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160941	GCTGCCGGATATGAT[A/G]TTGTGAACTCGGTGG	84628
rs572140828	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191228	TCCCGGGACAGTCCA[C/T]GCCATGAAGTTCCAG	84628
rs572167619	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169997	GGGGCGCCCTAATGG[C/T]GGCCAGATGCCCACT	84628
rs572207221	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222934	TGGGCAACACAGGGA[A/G]ACCCTATCTCCACAA	84628
rs572213387	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132226598	AGGAATCCTTGAAAC[C/T]AGCATCAGAGCAGAG	84628
rs572217944	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238927	CTCAAAGCAGGGAGG[C/T]CTCTCTCTTCCTGAA	84628
rs572218304	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185723	TTTCATTTACTTTTT[A/T]AAAAAGTATGAAAGT	84628
rs572328800	snp	A/G	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132174609	TGACCTCAGCTGGGA[A/G]CCAGCACAAAAGGAA	84628
rs572346982	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216593	CTCATGGGCTGGCCA[A/G]CATGCCCTATCTCTA	84628
rs572394151	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132204811	CTGGGTGTGGTGGCT[C/T]GTGCCTGTAATCCTA	84628
rs572402183	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168097	TCTGGTCATACAGGT[A/G]GGGTAACTGAGGCAG	84628
rs572438814	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160415	GTCACAGGGCTTTGG[C/T]GAAGATTCAGTGAAT	84628
rs572559751	snp	C/G	0.00795532	0.062565	intron-variant	NTNG2	GRCh38.p7	9:132173781	GAGAGGCAGGCAGGT[C/G]GAACCATACTGCGGA	84628
rs572599093	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228135	TCTGATGCTCAGACC[A/G]GGCCTGGGCAGTGGC	84628
rs572626172	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132173498	ACCCCCAGACCTTTC[C/T]GGTCTGCGCATCCCC	84628
rs572652811	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236741	ACCCCCAGAGGGAAG[C/T]CAAGGTAGTGACGAT	84628
rs572657443	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132215253	AAATCTGGCAACCAT[C/T]GTGGCATGGGGCTCT	84628
rs572677778	snp	C/T	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132181872	CTGGGCCGCCCGGCC[C/T]GGCATCCAGGTTCCT	84628
rs572696084	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209132	CGATTATGAGTAGAG[A/C]TGCTATAAACATTCG	84628
rs572764616	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206007	TTCTGGATTAGGTGT[A/G]ACCCTGGGCAAGTTG	84628
rs572828500	snp	C/T	0.000399281	0.0141238	intron-variant, splice-donor-variant	NTNG2	GRCh38.p7	9:132231791	CCCACAGCCCACAGG[C/T]GGGTGCCAGGGTACA	84628
rs572835744	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132178531	CAGTGAAATTGACTG[C/T]GCCCAGGAAAGGGGA	84628
rs572880555	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159745	ACCATCCTGGCAGTG[C/T]TAGGGAGGAGGCACC	84628
rs572917323	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132179221	ATGGCATCTGGTGGG[A/G]GACACAGGATGCCTG	84628
rs572925255	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184293	GTGCTGTGTCTACTC[C/T]TAAGACCTGGTTCTG	84628
rs573100861	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196555	CAGTATTATACGGCA[C/T]AGCCTCACTGTCCTA	84628
rs573101931	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183549	CTGACTGCCCCAGCC[C/T]GTCACCTCCAGGGCT	84628
rs573119547	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226360	CTCAAGGGCGTGGCT[A/G]TGGGCCACAACCTGA	84628
rs573185844	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132190211	GCACTCCAGACTGGG[C/T]GAAAGAGAGAGACTC	84628
rs573194841	snp	A/C			synonymous-codon	NTNG2	GRCh38.p7	9:132226963	CAAGAAGAATTTCCG[A/C]ACCCGGTCCTGGCGG	84628
rs573203465	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207457	TTGCGGCTGTCCGCT[A/C]CCTGAGCATCTGTCT	84628
rs573245302	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219360	GGAGGATCACTTGAG[A/G]TCAGGAGTTTAAGAT	84628
rs573268411	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243831	ACTCACAGTGTCCCG[A/G]GCCCACACACCAGCC	84628
rs573279750	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132222637	GGGAACTGAGCATCA[C/T]GGCACAGTGGATACA	84628
rs573327720	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132194644	GTCCTACCCTGGCCC[A/G]GGCCTCAGTCCCCCC	84628
rs573351522	snp	C/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244952	CACGAGGCTGGGGGC[C/T]CTGGAGCGTCAATGA	84628
rs573364545	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132195086	GTTAGTGACAGTGTT[A/C]GTTTTTTTCTTTCTT	84628
rs573398414	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243355	TGCAGAGACCCCAGA[C/T]GTGCCGGCCCTGTCC	84628
rs573432414	snp	A/G	0.0107246	0.0724382	intron-variant	NTNG2	GRCh38.p7	9:132182260	GGAGTGGGGGAAAAA[A/G]TTGCACCCAACAATG	84628
rs573453627	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175770	GGCTGCTGAGAGAGC[A/G]AGAATACGCCCCCAG	84628
rs573455978	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170157	GACCCAGGGGCGGAC[A/G]GCCTTTTCAGATGCG	84628
rs573456762	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160583	TCAGCAGTATAACTC[C/T]GTCTCCAGTTTTCAG	84628
rs573545986	snp	A/C	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132206929	AAGGCAGGTGGTTGA[A/C]CCCTGGACCTGCGGT	84628
rs573555699	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132191494	TCAAAGGAGAGAGCT[A/G]AGAGGGAACTCAGGG	84628
rs573582159	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201549	GGGGGATGTGGGACC[C/G]GAAGTTCCTGAGTGG	84628
rs573591252	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132170725	TGAGAGAGAGAGAGA[A/G]AACTACTGCCCAGGC	84628
rs573592920	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205085	CTGAACAAGTTACAT[A/G]TAGATTTAGCAATTC	84628
rs573630433	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132221543	ACAGTGCCAGCTCCT[A/C]CCTGCAGCCCTGCTA	84628
rs573652089	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242162	CGGGGGTCCCGGGGT[A/C]CCGGGGCGGGGCCGG	84628
rs573652649	snp	C/G			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132208838	AACCACCACCACAGC[C/G]TGGGCCCACAACAGC	84628
rs573706923	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230113	GGGACGCACTCCACC[C/T]GCGGCAGCCGCTCCC	84628
rs573714967	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132212120	CCACCATCACACCCT[C/G]CTCCTTCTCCTGTTT	84628
rs573765012	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132226564	AGGCAGTATCATCAC[C/T]CTCCCCAACTGAGAT	84628
rs573828868	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223941	CATTGCAGACCTCAC[A/G]GGTGGAACTTCTTTC	84628
rs573849118	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239642	TGGGGCTGGTGTGTG[G/T]GGGGGTCCCCCTCCA	84628
rs573859598	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132217974	GGGTGATGTGGCCGG[C/T]GTGGTCCATATCGCT	84628
rs573944159	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229184	AGGTGAGGCTGGAGG[C/T]GCTGCTGTCCTCAGC	84628
rs573985543	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233667	CAGCAACTGAAGCCC[C/T]TGTCCAGAGCCCCCA	84628
rs573994128	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241273	GGCCTAGTGAGAGCG[A/G]GGCAGGGTTGGGATA	84628
rs574024055	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234317	CCAGGCGTGAGCCAC[C/T]GCACCCGGCCAAGTA	84628
rs574092430	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132223978	AGGGCTTTCCTCATG[C/T]TCTTGCCTCTTTCTA	84628
rs574105150	snp	C/T	0.00279162	0.0372561	intron-variant	NTNG2	GRCh38.p7	9:132241759	CGCGCCTGGAGCCTC[C/T]TACATCCCCGGCCCA	84628
rs574141114	snp	C/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162689	GCTCCCGCGCCTCTC[C/T]CCCACCCCAATTCCA	84628
rs574252184	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132186657	AGGTCCTCCGAAAGG[A/T]TCTCAGGGTGTTCTG	84628
rs574297417	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221723	CAGCTGGGGAGGGAC[A/G]TCTGGATTTGGGTCA	84628
rs574316115	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132168779	TCTGTCTCTCGTATT[-/AG]AGTCTCGACTGTATT	84628
rs574332215	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191604	AGTCTTGCTCTGTCG[C/T]CCAGGCTGGAGTGCT	84628
rs574347882	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192678	GGAAGGTCAGGTCAG[C/T]GCCAACAGTGCCTTT	84628
rs574362233	snp	A/G	0.00438332	0.0466095	intron-variant	NTNG2	GRCh38.p7	9:132200139	AACAGTGCCTGGCAC[A/G]TAATACGCACTAAAA	84628
rs574363528	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210267	TAAAATGGGATCCCG[C/G]TCTTGTAAAGATTGT	84628
rs574377244	in-del	-/C	0.00179614	0.0299139	intron-variant	NTNG2	GRCh38.p7	9:132212932	CACATCTCTCCCAAC[-/C]CCCCCAAAGAAGACC	84628
rs574387882	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132193503	GCTCTGAGGTGGGAG[A/G]GGACGAAGTGGCCTG	84628
rs574400859	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132205001	AGGATGTGGAAAAAT[A/C]GGAACCTTCATGCAT	84628
rs574432929	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132222387	AGCAGTCCTGCAGCA[C/T]GCATGTGGCAATGGA	84628
rs574434111	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210709	GGTTGGAGAGGGGAA[G/T]TTGAGTGGGGAGAGG	84628
rs574478056	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161318	CTGACTCACTTGGCC[C/T]CCCTCCCTCGTGCCG	84628
rs574512697	snp	A/G	0.00478085	0.0486577	intron-variant	NTNG2	GRCh38.p7	9:132227453	TGGCCCCCATGGGAT[A/G]GCAGGGAGTGATGGG	84628
rs574586082	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184954	GAAAGACAAGGGAGA[C/G]AGGCAGAGCTGGTGG	84628
rs574594792	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191180	TGGCACTCAGTGAAT[A/G]TTACAATCATCACAC	84628
rs574609867	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132169298	TGTGTCCGATGAGGA[C/T]GGGGAGGCCGCCGTG	84628
rs574653578	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132185495	GGCCCTCTTTGGGAA[A/G]GCTGCCTGGGTCTAG	84628
rs574654433	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223111	AGAGTGAGACTCGGT[C/T]TCAAAAAGCAAAAAG	84628
rs574740960	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168031	GTAGGTAAAGTGTTC[A/G]GAATAGGACCTGGCA	84628
rs574754799	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132176973	GTGTGCTTCTTAGTC[A/T]TTTTTTTGTTTTTGT	84628
rs574779748	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160296	GTGAGAGAGCATCAC[C/G]CAGAAACCCAAAAGC	84628
rs574837705	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132195863	TCTTGAACTCCTGGC[C/T]TCAAGTGATCCTCCC	84628
rs574860339	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212935	CATCTCTCCCAACCC[C/T]CCAAAGAAGACCAAG	84628
rs574866004	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132232582	ACTCTGTGCAGTGCA[A/G]GTGCCAGGGGTCTGA	84628
rs574952516	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132164887	GCCTGAGGTGCTCAG[A/G]GCGCTCAGGGCAGCA	84628
rs575013493	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132177564	AGAGCCTATTCTTCC[C/T]CCACTAAATGTTCTT	84628
rs575068865	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221159	TGTGAAAGGCCTCCC[A/C]AAAGAAGTGGCATTT	84628
rs575108493	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132214492	CTCTCCCCTGGAGGT[A/G]AGGCCCGGTGCTGCC	84628
rs575116896	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132189263	CTTTTTTGTTTTTTG[A/C]GGTTTTTTTCTGTAG	84628
rs575140090	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132226341	GGGGGTTCTATCTGT[C/T]GCCCTCAAGGGCGTG	84628
rs575155012	in-del	-/CCCTGTGCTACCCTTTGGAGCCACCCCCTGCC	0.00398564	0.0444627	intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208870	GTCTCTCCAAGAACT[lengthTooLong]CCCGTCCCGAGACCC	84628
rs575172808	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132189546	GGGAGGGCACCTCTC[A/G]AATGAGCCTCATGTC	84628
rs575188796	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236613	TTTAGAGAGGGTCTG[A/G]GGCTCGGTTCCTAGA	84628
rs575216830	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218599	CCTGTTGGGTTCAAG[A/C]GATCCTCCTGCCTCA	84628
rs575219160	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244469	ACAGGCATGAGCCAC[C/T]GCACCACCTGCCTGT	84628
rs575229870	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183406	AACCCATTGCCCCCC[C/T]GCAGTGTTTTGTGTG	84628
rs575255667	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132219301	AAGATGGCTGGGCAC[A/G]GTGCTTCATGCCTAT	84628
rs575312190	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132166294	GTCCCAAAGAGGGAA[C/T]ATGTTTCCAGCTAAC	84628
rs575314699	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132184181	ACTTTACTCTTTCAT[C/T]GGCCCCACCGCCTCT	84628
rs575343610	snp	G/T	3.35464e-05	0.00409537	intron-variant	NTNG2	GRCh38.p7	9:132226837	ATCTCTGCCCTCTCG[G/T]TGTCTCCCCAGGTGC	84628
rs575344985	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207399	CCGGCAGCCTCTGGC[A/G]TTCCTGGGCTTGCAG	84628
rs575439692	snp	A/G	0.0134861	0.0810011	intron-variant	NTNG2	GRCh38.p7	9:132163384	GGCGGGGACCCAGGG[A/G]CCGGATAAAGGGCCC	84628
rs575457970	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132220657	CGGGGTTTCACCATG[C/T]TGACCAACTTCAACT	84628
rs575489060	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132236076	ACAGGAACCCCCCTC[C/T]CCAGCTGCCCTTGCT	84628
rs575489294	snp	A/C			utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242169	CCCGGGGTCCCGGGG[A/C]GGGGCCGGCGTCCGA	84628
rs575545083	snp	A/T	0.00398564	0.0444627	intron-variant	NTNG2	GRCh38.p7	9:132201979	CACAGCGCCACTACA[A/T]GGCAGACAGCTAACA	84628
rs575583461	snp	C/T	0.00597247	0.0543191	intron-variant	NTNG2	GRCh38.p7	9:132195742	TCAAGCAATCTCCAG[C/T]CCCAGCCTCCCAAGT	84628
rs575612600	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132213224	AAACTCAAGAGGTTG[A/T]GGCAGGAGAATCACT	84628
rs575618651	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132196483	AGGTGTGAGCCACCG[C/T]GCCCAGCCTGGGTCT	84628
rs575623689	snp	C/G	0.00318978	0.0398085	intron-variant	NTNG2	GRCh38.p7	9:132236186	GGTGGACTGTGGTGG[C/G]TGAAGGGAGAAGGCA	84628
rs575656625	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132207034	GGGTCACAGGAGGCT[C/T]GGGGAGCCCTGCAGG	84628
rs575663475	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176396	CTACTTTTTGTCTCC[A/G]TGAATTTAGCTATGC	84628
rs575685002	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171345	TCCTGGGAGAGGAAA[C/T]GCCTCTCACAACATA	84628
rs575692917	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222976	GAAATTAGCCAGGCA[C/T]GGTGGCACGCGACTG	84628
rs575730602	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172375	AGAGTTTAGAATCCC[A/G]TGCTGTGTGATCTCT	84628
rs575755857	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230067	GACGGCACGATTTAC[A/G]CAGGGGATGCTGACA	84628
rs575763215	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229762	GCCCAGGAGAAGCCC[A/G]TGGGCCACACATCCC	84628
rs575786409	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174667	TGGCTCAAGCCTGTA[A/G]TCCCAGCTCTGTGAG	84628
rs575799377	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176856	TTGTCAACACTTGTT[A/G]TTTTCTGGTTTTGTT	84628
rs575826663	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188506	AGCCGCATGACCCTG[C/T]GACATTGCTCAGCCT	84628
rs575837097	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132188074	CAAGCCATAGGGTTT[A/C]CCCCGAAATGGCAGA	84628
rs575844150	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194737	CCTGAGGACAGAGCT[A/G]TTTTGGTCAAAGAGG	84628
rs575899093	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132185043	AGCTGGAGACAAAGG[C/G]AAGGGTGTCTGGCTG	84628
rs575914920	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132175177	GAGACAGTCCACTCC[C/T]CCTGCCCACCTCATC	84628
rs575941450	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132211877	TCACCTTAGCACCAG[C/T]ACCCAGAACCAGGTA	84628
rs575959728	snp	C/G	0.00716266	0.059414	intron-variant	NTNG2	GRCh38.p7	9:132225564	TGTGCACCACCACGC[C/G]TAGCCTGTGTGGTTC	84628
rs575989497	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181823	TTGCCGAAGGCCACA[C/G]AGCTTCTAAGTAGAG	84628
rs576025880	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182182	CGAGCGTGCTCCCAC[A/G]CACCAGCTCTGGGGA	84628
rs576055164	snp	C/T	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132164584	CATCCAAACCTTTGC[C/T]GGCGGCGCTATTTTA	84628
rs576076647	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240422	ATATTCACCCTCTCC[C/T]ACAGAGCCCCAAGGC	84628
rs576144590	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216660	TGAAAAGTGCTGTGT[C/T]GGGGGATCAGGTGGC	84628
rs576187039	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241210	GGGACGGGGAAGAGG[A/C]GGTGGGCGGGGCCTC	84628
rs576210712	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132217131	ACCCATCTGAGCCTC[A/G]CATTCTCACCTGTAA	84628
rs576226435	in-del	-/A	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132165500	TAGTTTCTTACAGTT[-/A]AAAAAAAATTAAATT	84628
rs576308228	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132170102	CCAACATCCAGCCCA[C/T]GGGAGCGCAAGCCCG	84628
rs576327467	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161114	AAGCAGGGCCCATCA[C/G]GGTGGAGGCGGCGAT	84628
rs576357350	snp	A/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132233598	GAGGAGGTGGCTCCA[A/T]TGTGACAGCCAGTGG	84628
rs576364824	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174472	CCCGCACTTCTGGGA[C/T]GTGGGACTTGGGATA	84628
rs576425851	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132192452	AAAAATTAGCCAGGC[A/G]TGGTGGCGCACGCCT	84628
rs576454643	in-del	-/T	0.49949	0.0159663	utr-variant-3-prime, frameshift-variant	NTNG2	GRCh38.p7	9:132242390	CTTTCTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT	84628
rs576474063	snp	A/G	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132228184	GCATCCTCCCTCGAC[A/G]GGTGAAAGATTTATG	84628
rs576512147	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132228519	GGCCGCTCTCTCTTC[C/T]CTCCTCTCTGTCTCA	84628
rs576540479	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168559	GGGGAGAGAGAGAGG[A/G]AGGGAGAGAGGGAAG	84628
rs576573141	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132210098	TGACAACCCAGGGTG[G/T]CCCACCCTGGTGGCT	84628
rs576663280	snp	A/G	0.00453296	0.0473913	intron-variant, missense	NTNG2	GRCh38.p7	9:132231412	CAGAGATGCTTCTGG[A/G]GTGCACCGTCACCCT	84628
rs576674554	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201434	CGGTTGGGTTAGACG[A/G]TTCAGCGAAGGACTG	84628
rs576698145	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132233271	CTCCATATCACATGT[A/G]CAAGTGCACACATGC	84628
rs576741656	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132204893	CCAGCCTGGGCAATA[G/T]AGTGAGACCCCCATC	84628
rs576780278	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132205378	GACAAGTACCATATG[A/G]TTCTGCTTACCCGAC	84628
rs576816294	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132199265	CAGTGAATGGGCTCT[A/C]ATGTTCAGGGGTTTC	84628
rs576830061	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132216100	GAGGGGTCAGAGGTT[G/T]GAACCCGACTGTCTG	84628
rs576848316	snp	A/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132173807	GCGGATGAGACGGAC[A/G]GACGGACAGACAGGC	84628
rs576859743	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132208543	GCAGGGACAGGGGCT[A/G]TGATGTGGGCCGCCT	84628
rs576887903	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132168141	GGTAAAGGCATCTGG[A/C]CAAGGTCACACTCCA	84628
rs576892384	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132174038	GACGGACAGGCAGGC[A/G]GGCCACACCATGCTG	84628
rs576917592	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202100	GCTCTGACTTGAGCC[C/T]ACCTGGAGCTCAGGT	84628
rs576958937	snp	A/C	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132179274	TGGGGGCCGGAGCTG[A/C]CTCTTCAGGGTCAGT	84628
rs576997153	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132179849	TGTCACACAGGAGTT[C/T]GAATGGTCGTTCTGA	84628
rs577036966	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132191064	TACTTAGTGTCTTAT[C/G]TGAGACGTGGAGCTG	84628
rs577042705	in-del	-/AGAG			intron-variant	NTNG2	GRCh38.p7	9:132187594	GAGAGAGAGAGAGAG[-/AGAG]GGACAGAAAACGAGA	84628
rs577055953	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132169893	GACGCCACGCCTTGT[A/G]TTGCTAGTCTCTGGC	84628
rs577068745	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132183350	TGGCCTTCTCTCCTG[C/T]GCTCCCCACCAAGCT	84628
rs577118742	snp	C/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132221395	GGCCAAGAGGTCATA[C/G]ACAAACACCATGTCC	84628
rs577134784	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243907	CCCGGAAGTGCCTTC[C/T]GACAGGCCCTGCATC	84628
rs577150839	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132198696	TACCTGGGATGTTAC[C/G]TGGTATGTGGAACAT	84628
rs577179303	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132184373	GCTGTGTCAGGCTCC[A/G]CCCCTGCCTTCCTGA	84628
rs577201373	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194280	ATCACTCCTCCTCCC[A/G]AGCGGCACAGACAGA	84628
rs577217799	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132184909	CCTGGACAACAAGAG[C/T]GAAACTCTGTCTCAA	84628
rs577264836	snp	A/C	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236895	ACAGCGAAGGATTCA[A/C]TTCGGCTGGAGCAGG	84628
rs577273909	snp	A/G	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132197210	CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC	84628
rs577324418	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132182881	GGGAGCTTTTCATTC[C/T]CCCCCTGCCGCAGCT	84628
rs577354300	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132219726	TGGCTGTATAGTATT[C/T]ATTGCCTGCTTACAC	84628
rs577390682	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244384	GAGGTCTCACTATGT[A/T]GCCCAGGCTGGTCTC	84628
rs577411915	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132176974	TGTGCTTCTTAGTCA[A/T]TTTTTTGTTTTTGTT	84628
rs577424349	snp	A/C	0.00119737	0.0244387	intron-variant	NTNG2	GRCh38.p7	9:132213739	ACCCAAAGATAAATG[A/C]GCTATCTGGCAAGAG	84628
rs577449663	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132171858	CCTCCTTCCCCCTCT[A/G]TGTTTCTGGCCCCAG	84628
rs577487674	snp	C/T	0.00199481	0.0315187	intron-variant	NTNG2	GRCh38.p7	9:132172566	CCTGGACTGTGAGCT[C/T]CTCAAAGGCAGGGCT	84628
rs577498020	snp	A/G	0.00159617	0.0282053	intron-variant	NTNG2	GRCh38.p7	9:132226193	CGAGGTACAGTTTAT[A/G]TAGGACAGGCAGGAT	84628
rs577509346	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132165744	GGGATGCTTTTGAAA[A/G]TCTCTGACCCCCAAG	84628
rs577539604	snp	A/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132236044	TTCGGAGTCTGGTAG[A/T]GGCCCCGCCTCCCAC	84628
rs577684896	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230123	CCACCCGCGGCAGCC[A/G]CTCCCATGGCTTCTC	84628
rs577722265	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230490	CCAGGTGCTCCCCTG[C/T]CCTGCTGGCCCCTCT	84628
rs577726702	snp	C/G	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132171293	CCCTATCTGTAAAAG[C/G]GGTATGATCTTCACT	84628
rs577732280	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182731	TTTCCATCTCCCAAC[A/G]CTTGGGGCAGTCTTC	84628
rs577782110	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188601	TGAGGCACACAGGGC[A/G]CCCAGCACAGGGCCG	84628
rs577788852	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132234453	TCCCACACACCTGAG[C/T]GTGTCCCTGGGCAGC	84628
rs577824236	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132201650	AATTTCGTGACTGCC[A/G]TGTTGCCCAGTGGCT	84628
rs577828026	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229241	TGCCAGCAGGAAACA[C/G]CCCAAAGAGACACAG	84628
rs577828058	snp	C/T	0.000798403	0.0199641	intron-variant	NTNG2	GRCh38.p7	9:132234876	TCCGCACTTGTTAGC[C/T]GGTAGCTTTTCCTTT	84628
rs577843526	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203994	AGGGAGGTCCTTTGC[A/G]CCAAATTAAGGTCTT	84628
rs577846884	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242278	CGCCCGCACTGCCCT[A/C]CCCCCGCAGCAGGGG	84628
rs577890407	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212639	TCCTCGCTTTCTCAG[G/T]ATCTCAGGTTTGAAT	84628
rs577892224	snp	C/T	0.0023933	0.0345097	intron-variant	NTNG2	GRCh38.p7	9:132206615	GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCATTG	84628
rs577966211	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229644	GGTGTCCTCAGGGTC[G/T]AGCAGGTGGCTGCCC	84628
rs577987799	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132218007	TCAGGGCCAGTGTCA[C/T]TGGTGTGCGTGGCAG	84628
rs578053590	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211043	CATGGCTGCCTTGCA[C/T]CCCTGCTCACAGACG	84628
rs578103403	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181651	TATATCCTTCTCCTC[A/G]GAGCAGAAACATCGA	84628
rs578113924	snp	G/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132212182	ACCACCTGGGCCTGG[G/T]CCTTCCCTCGGGGGT	84628
rs578117955	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132200207	GTGAGAGGGCTGGGG[C/T]GGGCTGAGGGAGGAG	84628
rs578242968	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187185	AGCAGGGGCGGTCGC[C/T]GTGGCTTTGGGAGGC	84628
rs578251884	snp	A/G	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132181148	GAGTGCAGTGAAGCA[A/G]TCTTGGCTCACTGCA	84628
rs578252191	snp	C/T	0.000399281	0.0141238	intron-variant	NTNG2	GRCh38.p7	9:132187933	CGGTCATTTTGTGAA[C/T]GGGGAAACCAAGGCA	84628
rs745349451	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187919	AGCCCACTCCTGCCC[A/G]GTCATTTTGTGAACG	84628
rs745350123	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201358	TGGTGGCGAGAGTGT[A/G]CAATCAATTCAGAGA	84628
rs745382130	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132236404	CGCGCAGGCCTGCCC[C/G]ACTCTCCAGAAGGGA	84628
rs745400333	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132198980	TATCTACTTCTTGAG[A/G]TGTTACTTGGTTTCC	84628
rs745404153	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226008	AGTTGCTTTGGCTTC[A/G]GGTGGGGGTGTGTTC	84628
rs745419365	snp	G/T	1.67186e-05	0.0028912	intron-variant	NTNG2	GRCh38.p7	9:132239279	CTGCATTGGTGAGAG[G/T]GCACGGACACGGCAC	84628
rs745420910	snp	C/G	1.70621e-05	0.00292074	missense	NTNG2	GRCh38.p7	9:132198380	TCCAAGAAGGAGAAG[C/G]ACGTGCGCTTCGAGG	84628
rs745536714	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175924	AAACCACACAAAACA[A/G]TGGACTCCAGTGCAG	84628
rs745604473	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206231	TCCATGGACTCCCTG[A/G]AATATATGCTAAGTG	84628
rs745609589	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232265	CTTAGCCCCTCAGCA[A/G]CACACCGGTGGGATG	84628
rs745623926	snp	C/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132235705	GGTGGTCCCAGGTGG[C/T]CTCCCGTGCAGAAGG	84628
rs745631401	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132195349	AGTCTCGCTCTGTCG[C/G]CCAGGCTGGAGCGCA	84628
rs745703779	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132217260	CTTGCTTATTTATTT[C/G]ATTTACTTCATCTCC	84628
rs745719192	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205749	ACCTAGGTGTGGGAG[C/T]GGGTGCCTGTAATCC	84628
rs745791092	snp	A/G	0.000395847	0.014063	missense, stop-gained	NTNG2	GRCh38.p7	9:132242019	GATGACGGCGGTCTG[A/G]ACTGCGACCGCGCGC	84628
rs745881364	in-del	-/CCTT			intron-variant	NTNG2	GRCh38.p7	9:132183331	CTGGCTCCTGGCCTC[-/CCTT]TGGCCTTCTCTCCTG	84628
rs745904382	snp	C/T	2.72187e-05	0.00368898	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241043	GCGCCAGGGCTGCTA[C/T]CGTGAGTGCGCGCCG	84628
rs745907858	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205606	GGTAAGGTGGCTGGG[C/T]GCGGTGGCTCATGCC	84628
rs745956452	in-del	-/AGACTCTGTCTC			intron-variant	NTNG2	GRCh38.p7	9:132174910	CTGGGCGACAGAGCA[-/AGACTCTGTCTC]AAAAAAAAAAAGTGT	84628
rs745994197	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172041	CAGCTAACCACAAAT[A/G]GTGACACCGGGGCCT	84628
rs746016307	snp	A/G	1.74096e-05	0.00295034	missense	NTNG2	GRCh38.p7	9:132198270	CCGAGGACTGCATGG[A/G]GGCCTTCGGTATGTC	84628
rs746114865	snp	C/T	3.31455e-05	0.00407083	synonymous-codon	NTNG2	GRCh38.p7	9:132198121	GCTGGAAGCCAACAT[C/T]ACCCTTTCGTGGAAC	84628
rs746193213	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165584	TTCATGGTTGGCCAG[C/T]ACGTGGAGCACTCTG	84628
rs746205605	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132221418	CCATGTCCACACACA[C/T]CGACACAGAGGCAGT	84628
rs746235782	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132186616	TCTCCCGGGCAGCTC[A/G]TCCATCAGGGCAGCC	84628
rs746269953	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132220046	CCTGGTGAGTGTGAA[A/G]TGGTATCTCATTATG	84628
rs746275803	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240260	ATCAAAGCCGCTGAC[A/G]TCACAGGGGGCCAGC	84628
rs746283469	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132195501	TTTTTTTTTTTTTTT[-/G]TATTTTTAGTAGAGA	84628
rs746289962	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132193702	GAGCCATTCCTCCCG[G/T]CCTGTTCCCTCTTTG	84628
rs746293415	snp	C/G	6.61583e-05	0.00575107	missense	NTNG2	GRCh38.p7	9:132166943	ACCTGGGAGTTCTAC[C/G]CCTGCCAGCCCAAGG	84628
rs746304703	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132169421	TACTTCTAGATAGAT[C/G]TGGGTTCAAACCCTG	84628
rs746354028	snp	A/G	1.65056e-05	0.00287272	missense	NTNG2	GRCh38.p7	9:132166847	ATGCTGCATCTGCTG[A/G]CGCTCTTCCTGCACT	84628
rs746365619	snp	A/G	3.48955e-05	0.0041769	missense	NTNG2	GRCh38.p7	9:132226934	AACACCACCGGCCCC[A/G]ACTGCGGCAAGTGCA	84628
rs746376863	in-del	-/GAGA			intron-variant	NTNG2	GRCh38.p7	9:132170711	AGCTGACGAGCAGGT[-/GAGA]GAGAGAGAGAGAACT	84628
rs746383305	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235606	CCAGCTTCCCTCAGC[A/G]CCACCCCCTCGCATA	84628
rs746385913	snp	A/C	2.4446e-05	0.00349605	missense	NTNG2	GRCh38.p7	9:132226861	CAGGTGCAAGTGCAA[A/C]CTGCACGCCAACCTG	84628
rs746395201	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209061	TGTGCACTGCACACC[A/G]TGGTCTGTTTACCCA	84628
rs746408003	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167968	AAATGGGCACACTAA[A/G]AGCACACACTCCTAG	84628
rs746470896	snp	A/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208905	AAGCCCCCATCCTGC[A/T]CCCTGAAAATCTGCT	84628
rs746508355	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222541	TCACACAGACTTCAG[C/T]GGTGGCTAGTGCTGC	84628
rs746535169	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132165367	TAGCACAGCAATAAT[C/T]GTAATTGTAACCCAT	84628
rs746556584	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132207954	ACAAAAAATACAAAA[A/C]TTAGCCAGGCATGGT	84628
rs746562100	snp	A/T	7.33138e-05	0.00605405	intron-variant	NTNG2	GRCh38.p7	9:132239017	CTCCGTCCCTGCATG[A/T]CCTGGGGTGAGTCCT	84628
rs746641967	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187008	TCCCAAATAATGCGG[A/G]GTGAGGGGCGGTGAG	84628
rs746681759	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132199873	TGTGTTTTGAGGAAA[C/G]TTTGAGGAAGGCAAA	84628
rs746739933	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216077	ACCTTCCTGCCTTTG[C/T]CTAGCTTGAGGGGTC	84628
rs746761113	snp	G/T	0.000138773	0.00832871	intron-variant	NTNG2	GRCh38.p7	9:132241871	ACCGCCCCCTCCGCC[G/T]GCAGCCAACGTGTGC	84628
rs746770498	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175483	CCCCTGACCGGGGCT[A/G]ACCTGGCCAGAGTCC	84628
rs746785725	in-del	-/GGGAGGAGGAGGAGGAGT			intron-variant	NTNG2	GRCh38.p7	9:132185840	AGGAGGAGGAGGAGT[-/GGGAGGAGGAGGAGGAGT]GGGAGGAGGAGGAGG	84628
rs746917925	in-del	-/A			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244641	CTGAAACCCACCCTT[-/A]CCTTGGCCGCAGCCC	84628
rs746964658	snp	A/G			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244650	CACCCTTCCTTGGCC[A/G]CAGCCCCCCATGGTG	84628
rs746968043	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160324	AGCCCTGCCTCCCCG[A/G]CCACAATCCTTAGCT	84628
rs746968087	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176467	TTTGTGATGGCCTTC[C/T]TTCACTGGCAAAATG	84628
rs746974226	snp	C/T	1.65493e-05	0.00287652	synonymous-codon	NTNG2	GRCh38.p7	9:132239108	GGCCGGCCCAGACTG[C/T]GAATGCTACGGTCAC	84628
rs746974479	snp	C/T	1.7336e-05	0.00294409	missense	NTNG2	GRCh38.p7	9:132198293	GGTATGTCCGCCCGC[C/T]GGGCCCGCGACATGT	84628
rs747009918	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172088	GGGAAGGAGGAGGGC[A/G]TGCCCCTCCCCATGA	84628
rs747051342	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132171096	ATGCGGGCCTTGCTT[G/T]CCAAGGCGGGGGGTC	84628
rs747059431	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227291	CAGCTCCCAAACGCC[A/G]GGTCTCATAACAAGT	84628
rs747072964	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212163	AAATGGGCCTCTCTG[A/G]GCTACCACCTGGGCC	84628
rs747094943	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192857	GCTGTTGACTGAGCT[C/T]GCTCCACAGCAGGCG	84628
rs747115746	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132170073	CCCCTTCAGTGGCAG[C/G]TGCTACGTGTGTCCC	84628
rs747133075	snp	A/C	1.65671e-05	0.00287807	missense	NTNG2	GRCh38.p7	9:132198103	GAGCCGCTACCCCAG[A/C]CCGCTGGAAGCCAAC	84628
rs747163805	snp	C/T	3.37712e-05	0.00410907	synonymous-codon	NTNG2	GRCh38.p7	9:132197998	CAGCAACGAGTGTGA[C/T]GCCTCCAACCCGGAC	84628
rs747192397	in-del	-/TTTTT			intron-variant	NTNG2	GRCh38.p7	9:132189249	GCCCGGCTAGTTTTC[-/TTTTT]TGTTTTTTGAGGTTT	84628
rs747227067	snp	C/G	0.000173476	0.0093117	intron-variant, missense	NTNG2	GRCh38.p7	9:132231369	CTGGCCAATGTCAAA[C/G]AGCCAGCCGGGAGCA	84628
rs747248269	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132202234	CCAAGGGGGACCCCA[A/G]TGGCAGGCAGCAATG	84628
rs747255493	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132203420	GGTACCTATGGTACC[-/AG]CGGAAGCGATAGGGA	84628
rs747308941	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132218941	AGCTTTACCCAGATG[C/T]GATTCACACGTTGTA	84628
rs747349235	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229406	CCTCCATCCGCTCCA[A/G]GTCTCTCCCAATGCC	84628
rs747407842	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205420	CGTCAAATTCATAGA[A/G]ACAGAAAGTAGAATG	84628
rs747420590	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239876	GCTTTACCAGCCCAG[A/G]TCCAGCTATAAAGCT	84628
rs747444400	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203212	AGGCATGGTGGTGTG[C/T]GCCTGTAGTCCTAGC	84628
rs747444562	snp	A/C/T			intron-variant	NTNG2	GRCh38.p7	9:132190831	AGGCTCCTCCTCACC[A/C/T]GGTTCTCTGGTGCTA	84628
rs747470118	snp	C/G	1.77944e-05	0.00298276	intron-variant	NTNG2	GRCh38.p7	9:132198614	GTCATCGGCAGGTAA[C/G]GCCGGGGGAAGCCCT	84628
rs747486484	snp	A/T	1.73507e-05	0.00294535	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240910	CCCGTGTCCGTCCAG[A/T]GTGTAACTGCAACCA	84628
rs747487389	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132167141	GCTGGAGGACTGAGA[G/T]GCAAGGCTGACTTTC	84628
rs747535072	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186215	AAGGGGAGCCTTACC[C/T]TGTCTGAGACAGACG	84628
rs747548812	snp	G/T	7.16666e-05	0.00598566	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241027	TCCCCACGCACTACT[G/T]GCGCCAGGGCTGCTA	84628
rs747631730	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239583	AGAGCTGTGACTCTG[C/G]CAGGTGGCAGGCACT	84628
rs747631870	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132216292	TGTGTTAGACATTTA[C/T]CAAAAATTAAACCCA	84628
rs747633838	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132165849	TCTCCAAATGTGCAA[C/T]TCTGATATTAATAAA	84628
rs747634143	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179430	CCATCTGCCAGCTGC[A/G]GTCTTCTCTGTGGTG	84628
rs747666207	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191518	CTCAGGGCTTTCAGA[C/T]GCCAGGGCCCAAAAC	84628
rs747684321	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237645	CCCTCCTGGAGTAGC[C/T]GGGTCAAGGTTAAAC	84628
rs747721276	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177751	CAACCTCCCCCTCCC[A/G]GGTTCAAGCGATTCT	84628
rs747723195	snp	C/T	4.97327e-05	0.00498637	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166810	GGCTTCTCTGGGCCG[C/T]GCCTCTGCAGACTGC	84628
rs747827318	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225881	TGCCGGAGTTTCCTC[G/T]AGTCCAGATCTTGCG	84628
rs747850554	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207831	GGGCAAGGCCAGGCA[C/T]GGTGGCTCACGCCTG	84628
rs747851628	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175310	GGCTCCTGACCGCTC[A/G]CTAGGGTTAGGAAGG	84628
rs747868284	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218435	ACTCACGCATCAGCT[A/G]TCTACCCAGGAGACT	84628
rs747904601	in-del	-/TC			intron-variant	NTNG2	GRCh38.p7	9:132195964	TTTGTAGAGACAGGG[-/TC]TCTCTGTGTTGCCTG	84628
rs748002653	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185555	AGGGCGCTGTTCCTA[C/T]TCTCTAAGCATTTTC	84628
rs748074439	snp	C/T	2.21688e-05	0.00332925	intron-variant	NTNG2	GRCh38.p7	9:132239002	TCCAAAGATGCCTTC[C/T]TCCGTCCCTGCATGA	84628
rs748081770	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132214186	TCCGGCAGCCAGGAG[C/T]TGACCTACATTCCAC	84628
rs748108838	snp	A/G	4.97393e-05	0.0049867	synonymous-codon	NTNG2	GRCh38.p7	9:132198130	CAACATCACCCTTTC[A/G]TGGAACAAGACCGTG	84628
rs748128127	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132190190	GTGACCCGAGATAGC[A/G]CCACTGCACTCCAGA	84628
rs748220412	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132196519	TTTTGACTCATTCAT[A/C]ATGGCATGCATCCAC	84628
rs748226152	snp	C/T	2.54592e-05	0.00356777	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230576	CTCTCCCACAGGTGC[C/T]ACTGCAGGTTCCTTT	84628
rs748241354	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132181980	TGTGTGTGTGCGTGC[A/G]TGCAGCCATGTGTGC	84628
rs748258654	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132171048	AGGGGGTCCTGGGAA[C/T]GGAGGGATGGAGCTG	84628
rs748262869	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132224762	TTTCACTTTTTATTA[C/T]GGAGAATTTCCAACA	84628
rs748276012	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132232150	CCATCCTGACATGCA[C/G]CCAAAGACTGGCCTT	84628
rs748300477	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194949	TCCCCCATGGGGGCC[A/G]AACAGCTCATTTGAG	84628
rs748312950	snp	A/C	1.6534e-05	0.00287519	intron-variant	NTNG2	GRCh38.p7	9:132197916	AGAGGCTTCCCAGGC[A/C]ATCCCGAGCATCCAG	84628
rs748354485	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223462	AGCCTGTGGTGTCCA[A/G]GAGGATTTGGGGAGT	84628
rs748359192	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132169994	CAGGGGGCGCCCTAA[G/T]GGCGGCCAGATGCCC	84628
rs748396406	snp	A/C	0.000172548	0.00928677	missense	NTNG2	GRCh38.p7	9:132242003	CTGCGACCCCGCCGA[A/C]GATGACGGCGGTCTG	84628
rs748437523	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132169861	CCCGGGCTCCTTTGC[C/G]TCTCCCCAGCCTTGG	84628
rs748479961	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132238893	CCCTGGGCTCAGCCT[A/G]CTCAGGTTCTCCTCT	84628
rs748555982	in-del	-/TGTGTGTGTGTATGTG			intron-variant	NTNG2	GRCh38.p7	9:132216417	CTCTCTCTCTCTCTG[-/TGTGTGTGTGTATGTG]TGTGTGTGTGTGTGT	84628
rs748588136	snp	A/G	1.67756e-05	0.00289612	intron-variant	NTNG2	GRCh38.p7	9:132239295	GCACGGACACGGCAC[A/G]GGGAACTTGCTGGAA	84628
rs748638877	snp	C/T	1.7042e-05	0.00291903	synonymous-codon	NTNG2	GRCh38.p7	9:132197989	CTACCTATGCAGCAA[C/T]GAGTGTGACGCCTCC	84628
rs748681129	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132217833	CAGAACATCCCAGGC[A/C]AGTGGGGCCCAGGGG	84628
rs748724456	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132181645	TGATTCTATATCCTT[C/G]TCCTCAGAGCAGAAA	84628
rs748746496	in-del	-/CCGTGT	1.74278e-05	0.00295188	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240895	ACCGCGCGCCCGTGC[-/CCGTGT]CCGTGTCCGTCCAGA	84628
rs748800790	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132228057	GGCCCAGCGAACCTC[A/G]GGGCCCTCCCAGGTT	84628
rs748803940	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132202720	AAGAGAAGCGGGGCC[C/G]AAACCTGACCCAGCA	84628
rs748877108	snp	C/T	1.71431e-05	0.00292767	synonymous-codon	NTNG2	GRCh38.p7	9:132198583	CAAGTACTTCTACGC[C/T]ATCTCCAACATCGAG	84628
rs748890843	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132236960	TCCTTAAATGCCAAG[G/T]TTAGTCTCTGGGTTT	84628
rs748914006	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165557	GGGGGGCTGTTTCTC[A/C]GTGCCTGGCTCTTCA	84628
rs748953501	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206436	CTTTGGGAGGCCGAG[A/G]CAGGTCCATCACCTG	84628
rs749011051	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132193507	TGAGGTGGGAGGGGA[A/C]GAAGTGGCCTGGGAA	84628
rs749026127	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223648	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	84628
rs749061685	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197473	GAGAGTCGAGAATGT[A/G]AATGGGAATTTTTGA	84628
rs749108471	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132233268	ACTCTCCATATCACA[G/T]GTGCAAGTGCACACA	84628
rs749150580	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207077	AGTCACGCACAGCAA[C/T]GCCTTCCCAGCAGCA	84628
rs749170348	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212292	CTGGTCATACCCACC[A/G]TGTCACCCCTAAGCC	84628
rs749226749	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132224552	GGAGCCATCTGCTTT[G/T]TTGACATTATACTCA	84628
rs749307393	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132209705	GTTTCAGGGGTGAAT[A/G]CCAACACTTTTAAAA	84628
rs749311274	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132195617	CAGGCGTGAGCCACC[A/G]CGCCTGGCCTTTGTT	84628
rs749322436	snp	A/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231215	GGCGAGGGCGACATG[A/G]CGCCCACAGGTTATC	84628
rs749367496	snp	A/G	2.09751e-05	0.00323838	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132241992	GAGCAGCCCCGCTGC[A/G]ACCCCGCCGACGATG	84628
rs749385512	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160219	TTCATATCTCACATA[C/T]GGGGAAACTGAGCCC	84628
rs749397732	snp	A/G			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243429	GGGCAGCTTGGGAGT[A/G]GTGAGGAAGCTCCTA	84628
rs749409686	snp	C/G	1.75428e-05	0.0029616	missense	NTNG2	GRCh38.p7	9:132226961	TGCAAGAAGAATTTC[C/G]GCACCCGGTCCTGGC	84628
rs749512120	snp	C/T	0.000156789	0.00885268	intron-variant	NTNG2	GRCh38.p7	9:132241863	CCGTGCTGACCGCCC[C/T]CTCCGCCTGCAGCCA	84628
rs749530960	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132180773	GGAGAAATGCAGGGA[A/T]CCTACCCAGAAAACC	84628
rs749591095	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188495	AGCTGCTGCCGAGCC[A/G]CATGACCCTGCGACA	84628
rs749613468	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236508	TTCCTTCCAGCTCAC[A/G]TGTTCAAATTTCCTC	84628
rs749620015	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132224462	GTGCCACCTATTTAT[A/C]CTCCCTCCCTGTCCC	84628
rs749622236	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132169715	TGTCACGGTGCTGGC[A/G]GGACGGCACAGCCCG	84628
rs749623071	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132210935	TCACTCATCTGTAAC[A/T]TGCCCCTGACTCACA	84628
rs749627011	snp	C/T	1.65373e-05	0.00287548	synonymous-codon	NTNG2	GRCh38.p7	9:132239151	AGCTACATTGACTTC[C/T]TGAATGTGGTGACCT	84628
rs749632891	in-del	-/CCCATGCCCA			intron-variant	NTNG2	GRCh38.p7	9:132169598	TGCCTGTAGCCAAGG[-/CCCATGCCCA]CCCACCAGGCGGCAC	84628
rs749633984	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132186337	ACATTCCTGGAAATC[-/T]GGCTGTGGGAAGAAT	84628
rs749657832	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209210	CACCCAGGTGTGGAC[A/G]GCTGGGTCGTCTGGT	84628
rs749688051	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167648	TCCATTCCTACATGC[A/G]ATGATGGCAGCCCCT	84628
rs749697999	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222331	CCGTACCAATAGGTG[C/T]CTGCTGTCCCCCTCT	84628
rs749726395	snp	G/T	1.76157e-05	0.00296775	intron-variant	NTNG2	GRCh38.p7	9:132167068	ACTTACTGCTCTTTT[G/T]TTTGCCCAGGCCAAG	84628
rs749756559	in-del	-/TTTTTTTTTTTT			intron-variant	NTNG2	GRCh38.p7	9:132189069	GGCTTTAAGCCTTTC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT	84628
rs749779898	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237638	CCGAAAACCCTCCTG[A/G]AGTAGCTGGGTCAAG	84628
rs749799660	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132227249	CACACGTGCGTGCAT[G/T]CACCCCCACACACAC	84628
rs749814394	snp	G/T	1.64876e-05	0.00287116	missense	NTNG2	GRCh38.p7	9:132166959	CCTGCCAGCCCAAGG[G/T]GATGCGCCTGAAGGA	84628
rs749821393	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170892	AGGAAGTCTCTGGAG[C/T]GCTGGGGTGGGGTTG	84628
rs749904142	in-del	-/AGCCCGGCCGT			intron-variant	NTNG2	GRCh38.p7	9:132169724	CTGGCGGGACGGCAC[-/AGCCCGGCCGT]AGCCCGGCCGTGCTG	84628
rs749907230	snp	C/T			intron-variant, synonymous-codon, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237518	GCCTATTGAAGAATT[C/T]CAAGGTAAGAGGATG	84628
rs749930490	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132170480	CGAGAAGGAGGCAGG[A/T]AGGGCGACGGGCAAA	84628
rs749932516	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183589	TGCCACTCATGGGGA[C/T]CAGGACACAGGTGAC	84628
rs749933403	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211686	GAGCACCTCTCTGGA[A/G]CTCCTGAAGGCTGGA	84628
rs749965612	snp	C/T	6.65724e-05	0.00576903	synonymous-codon	NTNG2	GRCh38.p7	9:132198040	GCCCAGGCTCATGTT[C/T]GACAAGGAGGAGGAG	84628
rs749986138	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189745	CCCAGGTTCAAATGA[C/T]TCTCGTGCCTCAGCC	84628
rs750018686	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238681	ATACCACGGCGAGCG[C/T]CGTGAACCCAGGCGT	84628
rs750025192	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132210671	GCTGGGCCTCACCAG[C/G]TGCGATTGGGCAGGA	84628
rs750071151	snp	C/T	5.00371e-05	0.00500161	synonymous-codon	NTNG2	GRCh38.p7	9:132167035	CCCCCCTGAGAGGTT[C/T]TGCTCCCATGTAAGT	84628
rs750106732	snp	C/T	3.32441e-05	0.00407688	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230548	CCCTGGGGCAGCCAG[C/T]TCACGCCCGTCTCTC	84628
rs750110038	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132202681	GCGGGAGGGGCCTCC[A/G]CCCCCACCCTCCACA	84628
rs750143259	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132228285	GCAGGCGGTGAGACA[C/G]GCCTTTGAAGGGGTG	84628
rs750157743	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229795	TGCCAATCCCACAGC[A/G]TCCTTTCTCGGGAAC	84628
rs750179759	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132177397	TCAGCAGTATTTACC[A/C]CCATATTTTCTTCTA	84628
rs750184356	snp	C/T	1.66172e-05	0.00288242	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166789	ACCCCGTCGCTGCCT[C/T]TCCAGGGCTTCTCTG	84628
rs750211624	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191251	AGTTCCAGGGTTTCT[C/T]ATGCACAAGCCTGGT	84628
rs750244621	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204429	TAGAAACAGCAGAGG[A/G]AAGAAAACCATGGAG	84628
rs750257291	snp	C/T	1.70638e-05	0.00292089	synonymous-codon	NTNG2	GRCh38.p7	9:132198568	GCGGGAGAACCTCTA[C/T]AAGTACTTCTACGCC	84628
rs750282616	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132228850	GGCATGAGCCACCAC[A/G]TCTGGCCATGTCTGG	84628
rs750289830	snp	A/G	1.83185e-05	0.00302637	intron-variant	NTNG2	GRCh38.p7	9:132198634	GGGGAAGCCCTGGAT[A/G]TCACCTGCAACCTGG	84628
rs750306105	snp	G/T	1.81424e-05	0.00301179	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240963	TGCAACGAGACCGGC[G/T]TCTGCGAGTGCCGCG	84628
rs750385269	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132164285	TGCAATTAATAGATT[G/T]GCGAGTTGCGCCGCG	84628
rs750397705	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132178503	AAAAACCCCAATGTC[G/T]ATAAGCATGTTACAG	84628
rs750423072	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213928	GACCAGGAACCCCCA[C/T]GGTCCTGCAAAGAGG	84628
rs750437177	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132187504	CACAGAGAGCAAGAG[G/T]GACAGCGATCAATGA	84628
rs750487003	snp	C/T	1.69651e-05	0.00291243	synonymous-codon	NTNG2	GRCh38.p7	9:132198412	GCGGGACCGCTTCGC[C/T]ATCTTTGCCGGCCCC	84628
rs750532660	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235883	CGGGTGTAGAATGTC[A/G]GTGCCTGGGGAGCTC	84628
rs750606105	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160177	CCCTGTTTTTTGACC[C/T]CTCTTTGAAAAAAGA	84628
rs750648767	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132202740	CTGACCCAGCATCTC[-/A]CAGGAGAACCATTTA	84628
rs750678473	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188415	TTTTGGGTGAAGGGC[A/G]CCATTTCCCAATTTG	84628
rs750683274	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132231904	AGAGAGCAGGGGCTT[C/G]GCTCTTAGAATAGAG	84628
rs750683786	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132215624	TCTGGCAATATGTTA[A/C]TGAATCCTCCAAGAG	84628
rs750696147	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132178480	ATGCTGGGATTGTCT[A/G]AGGCCAGAAAAACCC	84628
rs750730095	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205896	AAAAGAAAAAAACAT[A/G]GTAAGGTGATAAATA	84628
rs750808199	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160950	TATGATATTGTGAAC[C/T]CGGTGGCCTCTGCCC	84628
rs750820354	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132198743	TGTTACCTGGTTCCC[G/T]GGGCGTTACCTGGTA	84628
rs750820510	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209017	GCCTGCGTGGCTCGG[A/G]CTCCTCACTCCTGAG	84628
rs750835267	snp	A/G	1.64852e-05	0.00287094	intron-variant	NTNG2	GRCh38.p7	9:132227026	TCCCAACGCCTGTAC[A/G]TGCCATGCCCCGGGG	84628
rs750846495	in-del	-/AAC			cds-indel	NTNG2	GRCh38.p7	9:132166660	TGTCGGCCTTTTGGA[-/AAC]AACAAGTTCCTCGCT	84628
rs750864492	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205303	GAGAACCTGACACAC[A/G]CTGCGACACAGATGA	84628
rs750881977	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216697	GATGGTTTTCTGGTG[A/G]GATTGATGGTTCCTG	84628
rs751108428	in-del	-/TC			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160712	GACCTTGGGCTGGTC[-/TC]TCTCTCTCTCTGCCT	84628
rs751137044	snp	G/T	1.65021e-05	0.00287241	missense	NTNG2	GRCh38.p7	9:132167000	GTGAAGGTGGAGCCC[G/T]CAGGCATCACATGTG	84628
rs751146920	snp	A/G			intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231767	CTGGGCCCCCATGGC[A/G]CCCAGCACCCCACAG	84628
rs751153319	snp	A/G	3.70858e-05	0.00430599	missense	NTNG2	GRCh38.p7	9:132227004	ACCTGCCGCTGCCCC[A/G]TGGCTCTCCCAACGC	84628
rs751156231	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132221332	AGAGAGACAAAGAGA[C/T]AGGAGAAGACGGAGA	84628
rs751219149	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182512	GTCTCTGCCCGCTCC[A/G]AAATGGAAAATTGTC	84628
rs751259104	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168728	ATCTCAAAGCCGGTG[A/G]GAGGGTTCTCCACAC	84628
rs751262455	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132210520	GGTATAGCCAAAGGT[A/G]CTTTGGAGGAGAGTG	84628
rs751273857	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132168876	ACCAGCTTTGGGTCG[A/C]GGGCTTGAGGTGGGG	84628
rs751327929	in-del	-/CT			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165996	GTTGTTGCTAATGAG[-/CT]CTCTCTCTCTCCTCC	84628
rs751335995	in-del	-/TC	0.000165057	0.00908303	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231282	GGGTGCCAGGCACGG[-/TC]TCTCCTTTCAGCCTT	84628
rs751350282	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132179050	GCCCAGAGGGTTGGA[C/G]TGACTTCCTTGAGCC	84628
rs751369962	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132197399	ATCTCAATAAAAAAA[-/T]AAAATTAAAATTAAA	84628
rs751372600	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132201270	GAGGCCTGAGGCTGC[C/G]TGGAGCCCATGTCTC	84628
rs751436623	snp	C/T	0.000133371	0.00816503	synonymous-codon	NTNG2	GRCh38.p7	9:132239261	GCTGGATGATGAGAA[C/T]GTCTGCATTGGTGAG	84628
rs751527314	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217003	CCCCATGGAATGGAC[A/G]CGAAGCCAGCACTGA	84628
rs751559182	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132234987	CCTTTGAAATTTGGG[A/C]ACAGGGCAGTTCTTT	84628
rs751585848	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132180712	AGAAAGAGAAAGAAC[C/G]ATAGAGAGATGCAAT	84628
rs751656950	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132215493	GCTGAGGCAGGATAA[C/T]TGCTTGAACCCAGGA	84628
rs751735356	snp	A/C	6.62285e-05	0.00575412	intron-variant	NTNG2	GRCh38.p7	9:132238970	GTGGGAGGCCTAGGG[A/C]ACCTTCCGGTACCTT	84628
rs751764024	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132173407	GAGGTTGGGTCCAGA[C/T]ACCCCGTGGAAGGCA	84628
rs751773984	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187373	TGCCAGGTTGGTTTA[C/T]GCTGATTCACGAGCG	84628
rs751815693	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197163	GGGAGGGCAAGCCAG[A/G]TGGATCAACGGAGGT	84628
rs751828787	snp	A/T			utr-variant-3-prime, synonymous-codon	NTNG2	GRCh38.p7	9:132242613	TTTTTCCTGCAACCC[A/T]CCAGACCCCAGGCCT	84628
rs751830413	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199114	CCTGAGCTTTTCCAC[A/G]GAAGAAGGTGCACAT	84628
rs751947453	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232732	GGGAGGACCTGGTGG[A/G]GACTCCTGGCCCCTT	84628
rs751984570	in-del	-/CC			intron-variant	NTNG2	GRCh38.p7	9:132236068	CTCCCACGACAGGAA[-/CC]CCCCTCTCCAGCTGC	84628
rs751988513	snp	A/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230984	CACCTGGATCTGGGA[A/G]AGCAGTCTCTCCTGC	84628
rs752029890	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213846	CAGTCTCAGTATACA[C/T]GACATGTAATAATGT	84628
rs752051314	snp	A/G	3.45477e-05	0.00415604	missense	NTNG2	GRCh38.p7	9:132198320	ATGTCATCCTCCAGC[A/G]CGCACCGCGTGCTCT	84628
rs752066958	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160813	CAGTGAGCCCACCCC[A/G]GGAGGCCAGGAGTGT	84628
rs752095736	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132193574	CTGGGTAGGTGACGC[A/C]GTGTGACGCCACTTG	84628
rs752141700	snp	C/T	1.69278e-05	0.00290923	missense	NTNG2	GRCh38.p7	9:132198227	TCCCTGGACAACGGG[C/T]GCACCTGGCAGCCCT	84628
rs752165255	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132185801	GGAAGGGAGGCGCCA[G/T]ACTGAGCCCCTGTGT	84628
rs752172894	snp	G/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208918	GCTCCCTGAAAATCT[G/T]CTGTAAGTGGAGTCG	84628
rs752224158	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193368	ACATTAACAACTCTA[C/T]GATGGATGATGAGAG	84628
rs752264935	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159945	CATCACTCACCCTGT[A/G]CAGGAGCCCCACACC	84628
rs752315376	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229991	TATTTCTCCCCAAGC[C/T]GTGTGTCCTCAGCTG	84628
rs752317576	snp	C/G	1.99424e-05	0.00315766	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240993	GAGGGCGCGGCGGGC[C/G]CCAAGTGCGACGACT	84628
rs752317733	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194272	ATCTGCCCATCACTC[C/T]TCCTCCCGAGCGGCA	84628
rs752330517	snp	A/G/T	0.00017516	0.00935706	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241091	CTGCGGAAAGGGGAC[A/G/T]GGGCAGGACCGAGGC	84628
rs752466798	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132175907	AGATTGGTCAGAGAC[-/A]AAAACCACACAAAAC	84628
rs752499865	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132208697	AATGGGGACAGAGGT[A/G]AGGGGATTTTCTGGA	84628
rs752510684	in-del	-/CA			intron-variant	NTNG2	GRCh38.p7	9:132210902	GTACCCGCCAAGTCA[-/CA]CACACACACGCAGCC	84628
rs752512528	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132210270	AATGGGATCCCGCTC[G/T]TGTAAAGATTGTCTG	84628
rs752537539	snp	C/G/T	4.99241e-05	0.004996	intron-variant	NTNG2	GRCh38.p7	9:132239087	CCATTGGTATTTCTC[C/G/T]CACTTGGCCGGCCCA	84628
rs752546167	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132221595	GGAAGAGGAGGCACT[A/G]TGCTTGTTCTGGGGC	84628
rs752565300	in-del	-/GTGTG			intron-variant	NTNG2	GRCh38.p7	9:132178664	CACTGATTAGGCCAA[-/GTGTG]GTGGCTCACACCTGT	84628
rs752634234	snp	A/G	1.64988e-05	0.00287213	synonymous-codon	NTNG2	GRCh38.p7	9:132166993	CGTCAAGGTGAAGGT[A/G]GAGCCCTCAGGCATC	84628
rs752658286	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132187726	ATTTATTCCCTCTGC[A/T]ACTTTTCTTACCAAT	84628
rs752727728	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132215641	GAATCCTCCAAGAGG[C/T]CAGGGGGTGTGTCAC	84628
rs752751550	in-del	-/C	3.12818e-05	0.00395473	intron-variant	NTNG2	GRCh38.p7	9:132226842	GCCCTCTCGGTGTCT[-/C]CCCCAGGTGCAAGTG	84628
rs752954662	snp	A/G			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166472	ATGCAGGATCCCTGC[A/G]GATTTTCTCCTTATC	84628
rs752980946	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217240	CAGCAAATTATTTCT[A/G]TGTGCTTGCTTATTT	84628
rs753005241	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132192463	AGGCGTGGTGGCGCA[C/T]GCCTGTAGTCCCAGC	84628
rs753009416	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212833	CACCTCTTACTCAAG[C/T]TGGCCTCTGCAGGCT	84628
rs753015008	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132195181	GAAAATTGAGCAGAT[A/G]GTACAGAAAGTACCT	84628
rs753071922	snp	A/C	1.68394e-05	0.00290162	missense	NTNG2	GRCh38.p7	9:132198213	TGGTCCTGGAGAAGT[A/C]CCTGGACAACGGGCG	84628
rs753090375	snp	C/T	0.000101735	0.00713141	intron-variant	NTNG2	GRCh38.p7	9:132238948	TCTTCCTGAATCCGA[C/T]GGAAGGGTGGGAGGC	84628
rs753096993	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132171715	GGAGTCCTTGAGCCA[C/T]TCCTCACTGTGACAT	84628
rs753110170	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186417	TACATTTTTAAGTTC[C/T]TGGAGAGATTAACCC	84628
rs753190951	snp	G/T	1.65701e-05	0.00287833	missense	NTNG2	GRCh38.p7	9:132198093	GCATCACCTGGAGCC[G/T]CTACCCCAGCCCGCT	84628
rs753208126	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213717	CCAAAACAAAAGAAC[A/G]CTCTTCACCCAAAGA	84628
rs753228701	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240058	TTGCCCCTGTCGTCA[C/G]TAGAGGCCAGGTCTC	84628
rs753282953	snp	C/T	0.000101652	0.00712851	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231322	CTCCCCCTGGGAGGT[C/T]GCCATCTGCTCTGCG	84628
rs753297835	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204887	TCAAGACCAGCCTGG[A/G]CAATATAGTGAGACC	84628
rs753415208	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229925	TCCCCCATCCCCTGG[A/G]CACACAGAGACACAC	84628
rs753447042	snp	A/G	1.93198e-05	0.00310797	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240982	GCGAGTGCCGCGAGG[A/G]CGCGGCGGGCCCCAA	84628
rs753450773	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132212621	CACGGCTCTGTTGTT[G/T]GTTCCTCGCTTTCTC	84628
rs753481592	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132193011	GCCAGCTGTGTCAGT[A/C]TTCCCAGTGACAGAC	84628
rs753485959	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132178701	ATCCTAGCACTCTGG[G/T]AGGCTGAGGCGGGCG	84628
rs753519937	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185194	ACTCTCAGCCCATCC[A/G]GAAACCTCTTTCAGC	84628
rs753524439	snp	C/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244637	AGAGACTGAAACCCA[C/T]CCTTCCTTGGCCGCA	84628
rs753534866	snp	C/T	5.25693e-05	0.00512659	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240876	GGCGCCCACACGTAG[C/T]CCTGACCGCGCGCCC	84628
rs753578749	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207782	AAACCCAGTACCCCC[A/G]AGTGCCCACAGGTGC	84628
rs753582591	in-del	-/TG			intron-variant	NTNG2	GRCh38.p7	9:132237202	AAGCTTGGGATGTGC[-/TG]TGTTTCCTTCAGGAA	84628
rs753604897	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132164703	GCAGGCTCTGTAACA[A/G]GTTCCCCTTTAAACA	84628
rs753612062	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132219379	GGAGTTTAAGATTAG[C/T]ATGGCCAACATGGCA	84628
rs753645106	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132217992	GGTCCATATCGCTCC[C/T]CAGGGCCAGTGTCAC	84628
rs753685021	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180007	CCCTGGAGTGTTCCA[A/G]AACTGCCCACCCTGT	84628
rs753715993	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239444	CAGAAAGCTCCAGAA[A/C]CTGCTCTATTAGTAA	84628
rs753771242	snp	A/G	3.59531e-05	0.00423972	missense	NTNG2	GRCh38.p7	9:132226889	CTGTGCTCCATGCGC[A/G]AGGGCAGCCTGCAGT	84628
rs753787113	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235127	GGTCAGGAAGGTAGA[A/G]GGGCAGTGATCAGGG	84628
rs753864792	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167735	GAAGGAGGGGTCCTA[A/G]GGGCACGGAGTACTT	84628
rs753872202	in-del	CTACTCGGGAGGCTGAGGCAG/GCTGAGGCA			intron-variant	NTNG2	GRCh38.p7	9:132215467	CGCCTGTAATCCCAG[lengthTooLong]GATAATTGCTTGAAC	84628
rs753902100	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227617	TGGGAACTGAGCTTC[C/T]GTTATCCCTTTTTAC	84628
rs753949417	snp	C/T	6.78104e-05	0.00582242	missense	NTNG2	GRCh38.p7	9:132198458	GACAACCTCTACACG[C/T]GGCTGGAGAGCGCCA	84628
rs753956899	in-del	-/AAAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213332	GTAAGACTCCATCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs754091505	in-del	-/C	1.66852e-05	0.0028883	frameshift-variant	NTNG2	GRCh38.p7	9:132239268	ATGAGAACGTCTGCA[-/C]TTGGTGAGAGGGCAC	84628
rs754091965	snp	A/G	3.32579e-05	0.00407773	missense	NTNG2	GRCh38.p7	9:132239235	GGCTACTACCGCAAC[A/G]GCTCGGCAGAGCTGG	84628
rs754117333	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132197042	GAGAGACCCAGAGCT[C/T]CCAGGCCCTCTTTGA	84628
rs754122947	snp	A/G	1.71711e-05	0.00293006	missense	NTNG2	GRCh38.p7	9:132198354	CCGAGGAGTACTCGC[A/G]CTGGGCAGGCTCCAA	84628
rs754128804	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236032	CCCTCCGAGGGCTTC[A/G]GAGTCTGGTAGAGGC	84628
rs754157692	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212502	AATTGCCGGCCTGAT[C/T]GCGTTCCAGGAGGCG	84628
rs754159327	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223334	CCCAGGGGACCCTTC[A/G]TTCCCACTCAGACAG	84628
rs754173843	snp	A/G	1.66059e-05	0.00288144	missense	NTNG2	GRCh38.p7	9:132198057	ACAAGGAGGAGGAGG[A/G]CCTGGCCACCTACTG	84628
rs754213608	snp	A/G	0.000165741	0.00910182	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231269	CCAGACACTCACAGG[A/G]TGCCAGGCACGGTCT	84628
rs754215960	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191810	ATCTCCTTACCTCAT[A/G]TCCACCCGCCTCAGC	84628
rs754263478	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232863	ATCAGCTCCTGCCTC[A/G]GCCTGTTGCTGGGTG	84628
rs754284603	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196123	AAAGTCCATAATTTA[C/T]ATGAGAGTTCACTTA	84628
rs754309960	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132206738	TGGGGACAGACATTT[C/T]GTTAAGTACAGTTCA	84628
rs754311452	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132211807	CGTACACGTCTGACA[C/G]CCGCCCCCATAGGCT	84628
rs754392128	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173448	TGAAAGGGCCCAGAT[A/G]GGACATCTTTCCAAA	84628
rs754447043	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171506	GAGTCTCCAGCATAC[A/G]GAGGCACCTTGGCTT	84628
rs754469495	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191394	GGGATTCTAGGTAAT[A/G]TGAGACACAGACCAT	84628
rs754473169	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229199	CGCTGCTGTCCTCAG[C/T]ACCCAAGTCTCCTGC	84628
rs754491842	snp	C/T	4.53258e-05	0.00476034	intron-variant	NTNG2	GRCh38.p7	9:132226802	AGAGGCCAGGCCAGG[C/T]TGCCCACAAGCTCTC	84628
rs754532121	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204944	GGAGGTACCCATGAG[A/G]ATGGCTATTATTGGA	84628
rs754580509	in-del	-/TC			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229642	GAGGTGTCCTCAGGG[-/TC]TAGCAGGTGGCTGCC	84628
rs754633846	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132219437	AATTAGCTAGATGTG[C/G]TGGTGGGTGCCTGTA	84628
rs754645109	snp	C/T	1.71519e-05	0.00292842	missense	NTNG2	GRCh38.p7	9:132198588	ACTTCTACGCCATCT[C/T]CAACATCGAGGTCAT	84628
rs754647344	snp	A/C	3.8771e-05	0.00440272	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240983	CGAGTGCCGCGAGGG[A/C]GCGGCGGGCCCCAAG	84628
rs754650774	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218587	CTGCAACCTCCACCT[A/G]TTGGGTTCAAGCGAT	84628
rs754669432	snp	G/T	2.48574e-05	0.00352535	intron-variant	NTNG2	GRCh38.p7	9:132238995	TACCTTTTCCAAAGA[G/T]GCCTTCCTCCGTCCC	84628
rs754682001	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132237041	GGTGTGCAATGTGAT[A/G]TCAATCTATCTAAAA	84628
rs754690173	in-del	-/TC			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237665	CAAGGTTAAACTGAG[-/TC]TCTCTTCCCTACAGG	84628
rs754703186	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229936	CTGGACACACAGAGA[C/T]ACACCTGGATTCAGG	84628
rs754709847	snp	C/T	0.000241279	0.010981	intron-variant	NTNG2	GRCh38.p7	9:132198642	CCTGGATGTCACCTG[C/T]AACCTGGGATGCTAT	84628
rs754771515	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132218253	AGTCCTGCGTCTGCC[C/G]CTTACCAGCTGTGGA	84628
rs754774220	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132167796	AACAGCAGAGATGGT[G/T]GCGTGCGAGCTGTCT	84628
rs754795430	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207796	CAAGTGCCCACAGGT[A/G]CACGGTGAGAAAGAA	84628
rs754846133	snp	A/G	3.32718e-05	0.00407858	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166782	CCGCCTGACCCCGTC[A/G]CTGCCTCTCCAGGGC	84628
rs754846759	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175100	CAGAAGGAATGGTTC[A/G]TGCAGAGACGCAGGG	84628
rs754865638	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132186751	AGCGGAGCGAAGCCC[A/G]CGGATGCCCACCGCC	84628
rs754904059	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132199281	ATGTTCAGGGGTTTC[C/T]GAGACCGCCCTCAGG	84628
rs754908562	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132235146	CAGTGATCAGGGAAG[C/T]AGGTCAGATGCTGGG	84628
rs754948793	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132225872	GGTCATTACTGCCGG[A/C]GTTTCCTCGAGTCCA	84628
rs755033307	snp	A/C/T			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161709	GAGAGATAAAAGCCC[A/C/T]GATGGTGATCGTGAG	84628
rs755116808	snp	A/C	0.000872068	0.0208632	missense	NTNG2	GRCh38.p7	9:132241993	AGCAGCCCCGCTGCG[A/C]CCCCGCCGACGATGA	84628
rs755116841	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216740	AGAGAGCGATCGCTT[A/G]GGAAAATTGATCCCA	84628
rs755126986	in-del	-/CCGGCCCAGACTGCGAATGCTACGGTCACTCCAACCGC	1.66957e-05	0.00288922	splice-donor-variant	NTNG2	GRCh38.p7	9:132239272	GAACGTCTGCATTGG[lengthTooLong]TGAGAGGGCACGGAC	84628
rs755237562	snp	A/G	1.69548e-05	0.00291154	missense	NTNG2	GRCh38.p7	9:132198459	ACAACCTCTACACGC[A/G]GCTGGAGAGCGCCAA	84628
rs755243066	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196439	CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	84628
rs755299540	snp	C/T	1.65792e-05	0.00287912	synonymous-codon	NTNG2	GRCh38.p7	9:132198085	CTGGCAGAGCATCAC[C/T]TGGAGCCGCTACCCC	84628
rs755338030	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132223341	GACCCTTCATTCCCA[C/G]TCAGACAGGGACAGA	84628
rs755350953	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132183164	CTCCTTCTGGCTTCC[A/T]GGGTGCCGAGGGGTG	84628
rs755402061	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132228597	GTCTCTCACTCTGTC[A/G]TCCAGGCTGGAGTGC	84628
rs755446437	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212631	TTGTTGGTTCCTCGC[C/T]TTCTCAGGATCTCAG	84628
rs755458803	snp	C/G	1.73857e-05	0.00294831	synonymous-codon	NTNG2	GRCh38.p7	9:132197974	GCTGCAGGAGAATCC[C/G]TACCTATGCAGCAAC	84628
rs755478528	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238770	TTCTAATCACCCCGG[C/T]ATGTGGGCATCCTTC	84628
rs755478809	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201929	TTCAGATGAAGAAGC[C/T]AAGGACTCTGAGGTC	84628
rs755504919	snp	C/T	0.000266809	0.011547	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230561	AGCTCACGCCCGTCT[C/T]TCTCCCACAGGTGCC	84628
rs755561803	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132211894	CCCAGAACCAGGTAG[G/T]CGTGCTGTATATGTG	84628
rs755608895	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211744	CTTCTCCAGCCTTGG[C/T]GGCTTGTGACAATTC	84628
rs755609005	snp	A/G	1.67309e-05	0.00289226	intron-variant	NTNG2	GRCh38.p7	9:132239280	TGCATTGGTGAGAGG[A/G]CACGGACACGGCACA	84628
rs755636458	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202686	AGGGGCCTCCGCCCC[C/T]ACCCTCCACACAACC	84628
rs755640887	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235557	GCTTCTAAGGGGCCT[A/G]TGGGGTGCGGGGCTG	84628
rs755653559	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204440	GAGGGAAGAAAACCA[C/T]GGAGGGTGGGCAGGT	84628
rs755658809	in-del	-/TC			intron-variant	NTNG2	GRCh38.p7	9:132226439	CAGCCCATGGCCAAG[-/TC]TCTGTCTACACCAGG	84628
rs755709416	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201420	CTTGTCGTTGAACTC[A/G]GTTGGGTTAGACGGT	84628
rs755790722	snp	A/C/T			intron-variant	NTNG2	GRCh38.p7	9:132228049	CAGACTGAGGCCCAG[A/C/T]GAACCTCGGGGCCCT	84628
rs755800178	in-del	-/TTGA			intron-variant	NTNG2	GRCh38.p7	9:132215690	GGCCTGGAGAATAGG[-/TTGA]TTATCTCTATTTTGG	84628
rs755821222	snp	C/T	0.000116324	0.00762553	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166792	CCGTCGCTGCCTCTC[C/T]AGGGCTTCTCTGGGC	84628
rs755849190	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206959	TCTCCTCTGGTCTTT[A/G]GCTCTGCTCCACTGC	84628
rs755880525	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132183260	GTCTTCCTGGAAGGA[-/G]GGGGCCGGCCAGCAT	84628
rs755883455	in-del	-/AAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213334	AAGACTCCATCTCAA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs755927722	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236899	CGAAGGATTCACTTC[A/G]GCTGGAGCAGGAAGA	84628
rs755982964	snp	A/G	1.853e-05	0.00304379	intron-variant	NTNG2	GRCh38.p7	9:132198641	CCCTGGATGTCACCT[A/G]CAACCTGGGATGCTA	84628
rs755986796	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177425	CTAAGACTTTTATAG[C/T]TTTAGCTCTTATATC	84628
rs756003517	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132197456	AGCTAAGGAGATATT[C/T]AGAGAGTCGAGAATG	84628
rs756037842	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132217864	ATGGGGTTACCATCT[C/G]TCAGTCACCCAGAAA	84628
rs756089798	snp	C/T	1.65652e-05	0.0028779	missense	NTNG2	GRCh38.p7	9:132239188	GCTGCAAGCACAACA[C/T]GCGAGGTCAGCACTG	84628
rs756142755	snp	C/T	1.70731e-05	0.00292169	missense	NTNG2	GRCh38.p7	9:132198575	AACCTCTACAAGTAC[C/T]TCTACGCCATCTCCA	84628
rs756162993	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204557	CTACAGGAAAAACAG[A/G]GGCAAGAAGGGAATT	84628
rs756181661	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132175258	ACTTCTCAGAGCCCA[C/T]TGAGTGTAGGAGCTG	84628
rs756211576	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132189411	AAGTACGATTGGCTT[-/A]AAAAAAAGGTATCAT	84628
rs756257616	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205365	CCAGACACAAAAGGA[C/T]AAGTACCATATGATT	84628
rs756262779	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226311	TGTGAATGAACTGAC[A/G]GGGGTGTGGGAGTTG	84628
rs756268365	snp	A/C			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244311	GCAGAGCCTGGGACA[A/C]CTGCCTTGGCTGCAA	84628
rs756295622	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213937	CCCCCATGGTCCTGC[A/G]AAGAGGTGCTTTGAG	84628
rs756306554	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176311	CAACACGTTTCCATC[A/G]CCCCAATAGAAAACC	84628
rs756334945	snp	C/T	1.72234e-05	0.00293452	synonymous-codon	NTNG2	GRCh38.p7	9:132198340	CCGCGTGCTCTGCAC[C/T]GAGGAGTACTCGCGC	84628
rs756385875	in-del	-/A			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243060	TAGGAGCCTCCCCAC[-/A]ACTGAAAGGCTGCCT	84628
rs756422154	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160202	AAAAGAAGGATTTAC[C/T]GTTCATATCTCACAT	84628
rs756424666	snp	A/T	1.6698e-05	0.00288941	intron-variant	NTNG2	GRCh38.p7	9:132239074	GAATGCTCGCTGACC[A/T]TTGGTATTTCTCCCA	84628
rs756432857	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196083	TCATGTCTGATGAAC[C/T]ATTGTTGATACATTA	84628
rs756492202	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167455	TCATCCTTTCTGTGG[C/T]GCAACCTCTTAGCCC	84628
rs756525267	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132169324	CCGTGGCAGGTGGAC[A/G]GCAGCCTTTTGCAGG	84628
rs756562871	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132224429	AAAGAATGGTTTCAC[C/T]GCCCTAAAAATCCCT	84628
rs756582910	snp	C/G	2.08392e-05	0.00322787	intron-variant	NTNG2	GRCh38.p7	9:132227035	CTGTACGTGCCATGC[C/G]CCGGGGCCACGAGCC	84628
rs756591960	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188331	CAGTCAAGAGACGTG[C/T]CGCCTGCCTCCCCGT	84628
rs756601614	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132183022	CCTCTCCCAGGCCTG[A/C]CCTGGAGCCCTTCCA	84628
rs756635649	snp	C/T	0.000108489	0.0073643	stop-gained, synonymous-codon	NTNG2	GRCh38.p7	9:132241980	GGCGTGCGCTGCGAG[C/T]AGCCCCGCTGCGACC	84628
rs756668076	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132199910	TCATAGGAGATGAAA[G/T]CAGCCTTTACCTCCC	84628
rs756705446	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132222085	CCAGGTCAGATTTTG[A/C]AGACAAACTCTTGTT	84628
rs756737426	snp	A/G			missense	NTNG2	GRCh38.p7	9:132166922	GTGACCACAGATGAG[A/G]GCCCCACCTGGGAGT	84628
rs756804596	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132235620	CACCACCCCCTCGCA[A/T]AACTTGGTTTCTTCT	84628
rs756837427	snp	A/C	1.65545e-05	0.00287697	missense	NTNG2	GRCh38.p7	9:132167020	CATCACATGTGGAGA[A/C]CCCCCTGAGAGGTTC	84628
rs756859665	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132221928	GGCAATCTTTTCTTT[C/T]GGTAGCTGATATCTA	84628
rs756923590	snp	C/T	1.96211e-05	0.00313212	splice-donor-variant	NTNG2	GRCh38.p7	9:132227023	CTCTCCCAACGCCTG[C/T]ACGTGCCATGCCCCG	84628
rs756934441	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201324	CCCAGCCTCTGCGGG[C/T]GGCGGGGAGGAGCCG	84628
rs756948924	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170357	AGCTCTCAACAGAGG[A/G]TTCTTGGGCGAGGAC	84628
rs756970935	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132236213	GGCAGCACATTCCAG[G/T]CCGCAGGGCCAGCCG	84628
rs756995312	snp	A/G	1.7063e-05	0.00292082	missense	NTNG2	GRCh38.p7	9:132198557	ACCTATGTGCAGCGG[A/G]AGAACCTCTACAAGT	84628
rs757000030	snp	C/T	3.29766e-05	0.00406045	synonymous-codon	NTNG2	GRCh38.p7	9:132166927	CACAGATGAGGGCCC[C/T]ACCTGGGAGTTCTAC	84628
rs757005449	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176506	GTTTGTCCACATTGT[C/T]GCATGACTCAGTGCT	84628
rs757050338	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132202344	GCCCTGGGAAGGAGG[A/G]ACTGGTACAAATGGT	84628
rs757050722	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132227866	GTGGAGAAGGCCACA[C/G]ACTGCCCCTGGGGTG	84628
rs757074728	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211723	TGCAACCAGCCCCTC[A/G]GTCCCCTTCTCCAGC	84628
rs757107490	snp	C/T	3.51068e-05	0.00418953	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240866	CCGAGAAGACGGCGC[C/T]CACACGTAGCCCTGA	84628
rs757112435	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132180716	AGAGAAAGAACGATA[C/G]AGAGATGCAATAACC	84628
rs757127202	snp	A/C/T			intron-variant	NTNG2	GRCh38.p7	9:132188798	GTGCTAGTAACCTCA[A/C/T]TGAGCGTTCATTCAT	84628
rs757167158	snp	A/G	3.39202e-05	0.00411812	missense	NTNG2	GRCh38.p7	9:132198470	ACGCGGCTGGAGAGC[A/G]CCAAGGGCCTCAAGG	84628
rs757167448	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132179118	AGGCCAAGGGCTCTC[A/C]CAGAGGTAGACTGGA	84628
rs757190398	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132218208	AGTGCAGACACTAAG[A/T]GTGGCTCTGAATCGA	84628
rs757197864	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132177298	AGCCTATTTTAAATT[G/T]AATGAACTCCAATGT	84628
rs757209178	in-del	-/CAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213331	AGTAAGACTCCATCT[-/CAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs757290644	snp	C/T	3.3379e-05	0.00408514	synonymous-codon	NTNG2	GRCh38.p7	9:132239270	TGAGAACGTCTGCAT[C/T]GGTGAGAGGGCACGG	84628
rs757319636	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186606	CAGTTGACCCTCTCC[C/T]GGGCAGCTCGTCCAT	84628
rs757322488	snp	G/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244674	CATGGTGACCCTCAA[G/T]TCACCAGGAAGAGGA	84628
rs757355835	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240423	TATTCACCCTCTCCC[A/G]CAGAGCCCCAAGGCA	84628
rs757518337	snp	C/T	6.0033e-05	0.0054784	intron-variant	NTNG2	GRCh38.p7	9:132238972	GGGAGGCCTAGGGCA[C/T]CTTCCGGTACCTTTT	84628
rs757521060	snp	C/T	3.31378e-05	0.00407036	missense	NTNG2	GRCh38.p7	9:132198105	GCCGCTACCCCAGCC[C/T]GCTGGAAGCCAACAT	84628
rs757551630	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193603	TGGTGCCAGCGTACT[A/G]AGAAACCAGGCTGGT	84628
rs757555599	snp	A/G	0.000180826	0.00950687	synonymous-codon, missense	NTNG2	GRCh38.p7	9:132241952	GCGCTGCGCCTGCCC[A/G]CGCGGCTACACCGGC	84628
rs757557180	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213109	GAGGTCGGGAGCTCA[A/G]GACCAGCCTGGCCAA	84628
rs757570430	in-del	-/AAGAGA			intron-variant	NTNG2	GRCh38.p7	9:132187569	AGAGCGAGAGGGAGC[-/AAGAGA]GAGAGAGAGAGAGAG	84628
rs757609008	snp	A/G	0.000412711	0.0143592	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231399	AGACCCCAAATCTCA[A/G]AGATGCTTCTGGGGT	84628
rs757613369	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132225706	CGTTCCATTTGTTTG[C/T]GTGTTTGATTTTACA	84628
rs757634343	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187900	GTCAGGGTCAGAGGC[A/G]GACAGCCCACTCCTG	84628
rs757641281	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204446	AGAAAACCATGGAGG[A/G]TGGGCAGGTGGGCGC	84628
rs757645581	snp	A/G	0.000104761	0.00723669	intron-variant	NTNG2	GRCh38.p7	9:132241838	GTTGGCGGGGGGACC[A/G]GGCCACCCCCCGTGC	84628
rs757661170	snp	G/T			intron-variant, utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242992	GCCCCCTCCCCGCAG[G/T]CTTGGCTGGCAGAGT	84628
rs757678730	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208936	GTAAGTGGAGTCGTG[C/T]GGCAGGTGGCTTTTT	84628
rs757733716	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232793	TCCAAGGAGACCTGC[C/T]CCACTGATCCTTCCC	84628
rs757737712	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132174915	CGACAGAGCAAGACT[C/G]TGTCTCAAAAAAAAA	84628
rs757803626	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180303	GGTGCTCCTGCCCTC[C/T]ACCAAGGCAGGCCAT	84628
rs757822617	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231099	CCTCTGCAGCCAGCT[C/T]GTCCCAGGGCTCTGC	84628
rs757872517	snp	A/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165163	TTGCCCTATTGGCCA[A/G]TATTTTTGGCCAGAA	84628
rs757899813	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193403	GGGTTCAAAGATTGA[C/T]TCAAGTCAGGAGGGC	84628
rs757927431	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185956	AGGGAAGTGTTTGAG[A/G]ATCACTGAGCTCCTG	84628
rs757942292	snp	C/G	3.2975e-05	0.00406035	synonymous-codon	NTNG2	GRCh38.p7	9:132166912	CAAATCCTGGGTGAC[C/G]ACAGATGAGGGCCCC	84628
rs757969256	snp	A/G	3.51519e-05	0.00419222	missense	NTNG2	GRCh38.p7	9:132226913	CTGCAGTGCGAGTGC[A/G]AGCACAACACCACCG	84628
rs757985144	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132219736	GTATTCATTGCCTGC[C/T]TACACATTTTGTTTT	84628
rs758079957	snp	A/C/T	6.84549e-05	0.00585008	synonymous-codon	NTNG2	GRCh38.p7	9:132198364	CTCGCGCTGGGCAGG[A/C/T]TCCAAGAAGGAGAAG	84628
rs758080480	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181461	AAGTAGCTGGGATTA[C/T]AGGCACCTGCCACCA	84628
rs758105727	snp	A/G	1.65701e-05	0.00287833	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166811	GCTTCTCTGGGCCGC[A/G]CCTCTGCAGACTGCG	84628
rs758119397	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132187783	ATTCCCCTAGCACCC[C/T]GGCTTTCTCCCTGGA	84628
rs758132647	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167909	AGCGTCAGGGGAGGG[C/T]TCTGGCCCAGTGACG	84628
rs758181629	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132221132	TAGCAGGGGCTGATT[G/T]GAGGTAGGGGTTGTG	84628
rs758191774	snp	C/T	7.15538e-05	0.00598095	intron-variant	NTNG2	GRCh38.p7	9:132226834	GACATCTCTGCCCTC[C/T]CGGTGTCTCCCCAGG	84628
rs758215512	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236080	GAACCCCCCTCTCCA[A/G]CTGCCCTTGCTCACA	84628
rs758223464	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225909	GCGGATGGCATCCCC[G/T]GGTGTCGTTCAGGGT	84628
rs758265183	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132200294	GTGCAGGCAGGGGCT[A/G]CACCTGGGGAGCCCA	84628
rs758283244	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233243	CAGGGGTTTGGCTGG[A/G]AGGCCAGATACTCTC	84628
rs758298878	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132178731	GGATTGTCTGAGCTC[A/G]GGAGTTTGAAACCAG	84628
rs758318272	snp	A/G			missense	NTNG2	GRCh38.p7	9:132198257	TACCAGTTCTACGCC[A/G]AGGACTGCATGGAGG	84628
rs758320291	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132223829	GCCACAGCGTTATAA[A/C]ATATGGCCCAGAGCA	84628
rs758322098	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132175318	ACCGCTCGCTAGGGT[A/T]AGGAAGGATTAGGCC	84628
rs758333536	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227673	AGAGTCCCCCCGCAC[A/G]TGCTCTCTGCCCACC	84628
rs758425408	snp	A/G	1.64988e-05	0.00287213	synonymous-codon	NTNG2	GRCh38.p7	9:132166996	CAAGGTGAAGGTGGA[A/G]CCCTCAGGCATCACA	84628
rs758439510	in-del	-/TGTG			intron-variant	NTNG2	GRCh38.p7	9:132216429	CTGTGTGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT	84628
rs758449050	snp	C/T			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166511	ATCCACTGTCACAAT[C/T]TGAGAATCTGCCTGA	84628
rs758482786	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132171836	CTGACCGGCCCGATG[G/T]CTCTGGCCTCCTTCC	84628
rs758526096	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132224262	TGCACAGTTTCCCCT[A/G]TTTTGGAGTATATGT	84628
rs758539268	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132165048	GGAGAGCCAGGTCCA[C/G]ACTGGACATTTGGGG	84628
rs758577422	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132196520	TTTGACTCATTCATA[A/G]TGGCATGCATCCACC	84628
rs758595425	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132211943	TCAGTCAGTCAGTCA[G/T]TCATTTATTCATTCA	84628
rs758739450	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132173218	GCACCAGCCGTTAAA[G/T]CCACTCAGTCTCTTG	84628
rs758780410	in-del	-/AA			intron-variant	NTNG2	GRCh38.p7	9:132205343	ACATGATGCTAAGTG[-/AA]ATAAGCCAGACACAA	84628
rs758791747	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212915	GCTTGCCTGAGCCAA[A/G]GACACATCTCTCCCA	84628
rs758834216	snp	C/G	0.000165645	0.00909918	synonymous-codon	NTNG2	GRCh38.p7	9:132198100	CTGGAGCCGCTACCC[C/G]AGCCCGCTGGAAGCC	84628
rs758919372	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230029	AGGACCATAAGGAAG[C/T]TCCCTCATAGGGTTC	84628
rs758922529	in-del	-/TCCA			intron-variant	NTNG2	GRCh38.p7	9:132225800	TTCTCTTGCTCTAGG[-/TCCA]TCCTTTTTCCGTATC	84628
rs758943421	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191747	CGGCTAATTTTTTGT[A/G]TTTTTTAGTAGAGAC	84628
rs759012237	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203462	CTGGGGAGAAATGGA[A/G]ACAGCAGGCGCCTCA	84628
rs759035182	in-del	-/AAG	1.66341e-05	0.00288388	cds-indel	NTNG2	GRCh38.p7	9:132198044	AGGCTCATGTTCGAC[-/AAG]GAGGAGGAGGGCCTG	84628
rs759067579	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213634	GCATCTCCAAGCCAC[C/T]GTAAGATCTGGGATT	84628
rs759155907	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187094	AGCCGAGGCAGGTTC[A/G]AGAGGCAGCCAGAGA	84628
rs759200456	snp	G/T	1.67388e-05	0.00289294	synonymous-codon	NTNG2	GRCh38.p7	9:132198187	CTTCGAGTACGGCCG[G/T]CCCACGGTCATGGTC	84628
rs759223913	snp	A/G	1.73135e-05	0.00294218	missense	NTNG2	GRCh38.p7	9:132198300	CCGCCCGCCGGGCCC[A/G]CGACATGTCATCCTC	84628
rs759242424	snp	A/G	1.71076e-05	0.00292464	intron-variant	NTNG2	GRCh38.p7	9:132239038	GGTGAGTCCTTCCTC[A/G]CCCTGTCCCTCAGTT	84628
rs759250473	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243829	GGACTCACAGTGTCC[C/T]GAGCCCACACACCAG	84628
rs759315854	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132221801	ACCCAGCCTGTCCAG[A/C]TCTGACATCCAATGG	84628
rs759352128	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132181082	CTGGTCCAATTGTCT[A/G]AGGACTTTCTCTTTT	84628
rs759420043	snp	A/G	1.64939e-05	0.0028717	missense	NTNG2	GRCh38.p7	9:132166985	AAGGACTACGTCAAG[A/G]TGAAGGTGGAGCCCT	84628
rs759459399	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132168341	CAGCTGGTACCTCTG[C/T]GTGTCCTTGGAGGAG	84628
rs759475604	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218012	GCCAGTGTCACTGGT[A/G]TGCGTGGCAGCCTGT	84628
rs759512166	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132209911	GACTGAAGATAGCTG[A/T]GGGGAGGGCGGGAGG	84628
rs759546568	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132182175	TTGGCAGCGAGCGTG[C/G]TCCCACGCACCAGCT	84628
rs759548195	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168640	ACTGCCCCGGGGACC[A/G]CAGGGCCAAGCAAGG	84628
rs759552257	snp	A/G	1.78109e-05	0.00298414	missense	NTNG2	GRCh38.p7	9:132226896	CCATGCGCGAGGGCA[A/G]CCTGCAGTGCGAGTG	84628
rs759566237	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132190944	GCCTATGTGTGTCCA[C/G]AGAGATAGGAAAGCT	84628
rs759578206	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202468	GTCCCAGCCACGCCC[C/T]CTCCCTGCCTCCCGC	84628
rs759612086	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229547	ACCTCCCCGTGCCCT[A/G]CCTGATGTCCCGCCT	84628
rs759628452	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132181934	TGGATCTCAGAAAGC[A/G]CCTGATAGACGGAGG	84628
rs759744267	snp	C/T	1.70837e-05	0.00292259	missense	NTNG2	GRCh38.p7	9:132198543	CGGCGCTGGGCGGCA[C/T]CTATGTGCAGCGGGA	84628
rs759744268	snp	C/G	3.50877e-05	0.00418839	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240942	ATAGGCTCCGTGCAC[C/G]ACCGGTGCAACGAGA	84628
rs759760609	snp	A/G	1.7569e-05	0.00296381	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240861	GGGGTCCGAGAAGAC[A/G]GCGCCCACACGTAGC	84628
rs759793334	in-del	-/AGAG			intron-variant	NTNG2	GRCh38.p7	9:132187572	GCGAGAGGGAGCAAG[-/AGAG]AGAGAGAGAGAGAGA	84628
rs759825418	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206757	AAGTACAGTTCACAC[A/G]CCTTCAACTGCATCT	84628
rs759938575	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132219310	GGGCACGGTGCTTCA[G/T]GCCTATAATCCCAGC	84628
rs759943164	snp	A/G	5.18793e-05	0.00509284	missense	NTNG2	GRCh38.p7	9:132198302	GCCCGCCGGGCCCGC[A/G]ACATGTCATCCTCCA	84628
rs760002393	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132166321	TAACATGCCCACCTC[C/T]TGATTTTATTTTATC	84628
rs760003956	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132225365	AGCCTTGAACTCCTG[A/G]GCTCAAGGGATCCTC	84628
rs760132640	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132171591	CTTACTCAGTTAGAA[A/C]CTGCTTTAGCTTCTC	84628
rs760220558	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183856	TGGTTAATTACTCGA[C/T]TGGTTAGTTTGTTGG	84628
rs760241785	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173345	AGAAGACCGAGGCCC[A/G]GGGCCCAGGGAGTGA	84628
rs760265929	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132171436	TTTATCCAATCTTGA[A/T]AAGCTTGACATTTCT	84628
rs760310055	snp	C/T	0.000231134	0.0107477	intron-variant	NTNG2	GRCh38.p7	9:132238919	CCTCTGGGCTCAAAG[C/T]AGGGAGGCCTCTCTC	84628
rs760320075	in-del	-/A			intron-variant	NTNG2	GRCh38.p7	9:132221405	TCATACACAAACACC[-/A]TGTCCACACACACCG	84628
rs760326589	snp	C/T	2.41537e-05	0.00347509	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230645	CCACTGCACGAGCCT[C/T]TTTGCATGTCCTGGA	84628
rs760328828	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172229	TTTTTCAAGGTTCAG[A/G]TTGGACCCTACCTCC	84628
rs760332634	in-del	-/A	3.48183e-05	0.00417228	intron-variant	NTNG2	GRCh38.p7	9:132167062	AGTCCACTTACTGCT[-/A]CTTTTGTTTGCCCAG	84628
rs760408444	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132219163	CAGACATTGCAGTGA[G/T]CTGTGATCGTGACAC	84628
rs760552195	snp	G/T	4.17859e-05	0.00457069	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241077	CCCGTGGGCGGGGCC[G/T]GCGGAAAGGGGACGG	84628
rs760571702	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132220306	TTGTCTTTTCACTTT[C/T]CTGACAGTGTCCTCT	84628
rs760628653	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188532	AGCCTCTCTGAGTCT[C/T]GGTTTCCTGAGGATC	84628
rs760667088	snp	A/C	3.3325e-05	0.00408184	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241061	TGAGTGCGCGCCGTC[A/C]CCCGTGGGCGGGGCC	84628
rs760676699	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132179978	TCCAGGTGTGTGGAT[C/T]CCTGTGAATCTAACC	84628
rs760699977	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194051	CAATCACCTCTTGAA[A/G]GAGAATCTGTCTCCA	84628
rs760703132	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132236863	GCTTGACAGCACTTG[C/T]GAGTGGGACTCCAGG	84628
rs760715768	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211234	AAAGCCCCCTCTGGG[C/T]TTCTAACCATCCCTC	84628
rs760756729	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132164585	ATCCAAACCTTTGCC[A/G]GCGGCGCTATTTTAT	84628
rs760759085	snp	A/G	1.85469e-05	0.00304517	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240969	GAGACCGGCTTCTGC[A/G]AGTGCCGCGAGGGCG	84628
rs760777833	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201736	TCATTTGCTATTGAG[C/T]GCTGTTATTAACGGC	84628
rs760786911	snp	A/G	1.65679e-05	0.00287814	synonymous-codon	NTNG2	GRCh38.p7	9:132239192	CAAGCACAACACGCG[A/G]GGTCAGCACTGCCAG	84628
rs760788737	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132200590	TGTGCCGTGAGGCTG[G/T]GCAGGCCGCTGTGGT	84628
rs760814464	in-del	-/GACG			intron-variant	NTNG2	GRCh38.p7	9:132174314	GCTGCGGATGAGACG[-/GACG]GACGGACGGACGGAC	84628
rs760830162	snp	A/G	1.88113e-05	0.00306681	intron-variant	NTNG2	GRCh38.p7	9:132197924	CCCAGGCCATCCCGA[A/G]CATCCAGCACCCACC	84628
rs760937167	in-del	-/CAAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213331	AGTAAGACTCCATCT[-/CAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs760940849	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161628	CACCTTTAAGAAGAC[A/C]GTTGCTCCGTGGTGG	84628
rs760954492	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181862	CACCTCCAGCCTGGG[C/T]CGCCCGGCCCGGCAT	84628
rs761069887	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132196953	GAACTCAGAAAGGCA[G/T]TTTCCCTACATTTAC	84628
rs761175807	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132233489	GGTGAGGGTCCCCAG[C/G]ACCCCCTCAGTGAGC	84628
rs761188278	snp	C/G	0.00145367	0.0269206	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230638	AGGGCCCCCACTGCA[C/G]GAGCCTCTTTGCATG	84628
rs761215788	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232741	TGGTGGGGACTCCTG[A/G]CCCCTTGGGTAGTGC	84628
rs761272918	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196838	CCACCTCTGACGCAA[C/T]TGCAAGTTCCTGCCT	84628
rs761332702	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223147	ATTGCCTGGATTTAC[C/T]ATAATTTCCCTAACC	84628
rs761353879	in-del	-/C			utr-variant-3-prime, frameshift-variant	NTNG2	GRCh38.p7	9:132242407	TTTTTTTTTTTTTTT[-/C]TGGCGGTGAGCCAGA	84628
rs761433166	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206602	AACCCAGAAGGCGGA[A/G]GTTGCAGTGAGCCGA	84628
rs761468908	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132183566	TCACCTCCAGGGCTT[A/G]TCATCTGTGCCACTC	84628
rs761471311	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132164228	GGGTTTTTTAAATTT[A/G]TTTATTTTCCAGGGA	84628
rs761582581	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171464	TCTACATTGACATGG[A/G]TGAACATTCAAATTT	84628
rs761617116	snp	C/G/T	5.29716e-05	0.00514621	missense, synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240950	CGTGCACGACCGGTG[C/G/T]AACGAGACCGGCTTC	84628
rs761624790	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132238662	TGCATTCATCTACCC[A/G]AGGATACCACGGCGA	84628
rs761647566	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132172131	CTCCAGCCTTGGCCC[A/G]TGCTGTCTCCTCCAC	84628
rs761666324	snp	A/G	1.67091e-05	0.00289038	synonymous-codon	NTNG2	GRCh38.p7	9:132198025	GGACCTGGCCCACCC[A/G]CCCAGGCTCATGTTC	84628
rs761715178	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227994	CCCTCACACAGCCCC[A/G]CAGGGTGGAGTCCTT	84628
rs761781350	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182931	GCAGCCTCTCTGGGC[A/G]GCCCAGCAGGAGGAG	84628
rs761810668	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132209667	AGAGCCCGGGAGTCC[A/G]GGATGAAGGCCGTCG	84628
rs761826584	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203620	CAAGGAAAACAAAAT[A/G]CCCCTGCAGCCCAGG	84628
rs761846223	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132221379	CTGAGAGAGCCAGAG[A/C]GGCCAAGAGGTCATA	84628
rs761868881	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180907	CTCATGCACAGGCAC[A/G]CACACACACATATAA	84628
rs761900702	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132208350	CCAGATCACGCCAGC[C/T]CTGCAGCCCCGGGAG	84628
rs761934627	snp	C/T	3.347e-05	0.00409071	intron-variant	NTNG2	GRCh38.p7	9:132239069	TCCCTGAATGCTCGC[C/T]GACCATTGGTATTTC	84628
rs761949972	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132223342	CCCTTCATTCCCACT[-/C]CAGACAGGGACAGAG	84628
rs761956522	snp	C/T	3.5407e-05	0.0042074	missense	NTNG2	GRCh38.p7	9:132226967	AAGAATTTCCGCACC[C/T]GGTCCTGGCGGGCCG	84628
rs761967967	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199371	GGTTTATTACAATGA[A/G]GGATACAGATTAAAA	84628
rs761991881	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132166212	ATTCTAGTCCAGTCA[C/T]ACAGCTGTTGCCACC	84628
rs762081062	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200295	TGCAGGCAGGGGCTG[C/T]ACCTGGGGAGCCCAG	84628
rs762098503	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132226178	AACTTTCGGTTACCC[C/T]GAGGTACAGTTTATA	84628
rs762105048	snp	C/T	1.64972e-05	0.00287199	missense	NTNG2	GRCh38.p7	9:132166865	CTCTTCCTGCACTGC[C/T]TCCCTCTGGCCTCTG	84628
rs762148209	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180206	AAGGAAATGAAACAC[A/G]ACCAGGCATTTTCCC	84628
rs762216171	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132205836	CAGTGAACTGAGATC[C/G]CACCACTGCACTCCA	84628
rs762221124	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176115	GCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCAC	84628
rs762262520	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132215238	GTATTTTTATTTGGG[A/T]AATCTGGCAACCATT	84628
rs762267322	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244188	TTTTTCTCTCTCATC[C/T]CTCCCTCTGCTCTTC	84628
rs762274772	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132236985	GGGTTTGATGCTCCA[-/G]GAAGTTTGGAGAGGC	84628
rs762294655	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132227322	CCCTCTAGCATACCT[C/G]CATCCTGCTGAATGC	84628
rs762306388	in-del	-/ATTC			intron-variant	NTNG2	GRCh38.p7	9:132211914	CTGTATATGTGTGGA[-/ATTC]ATTCATTCATTCAGT	84628
rs762306736	snp	A/C	1.70769e-05	0.00292202	synonymous-codon	NTNG2	GRCh38.p7	9:132198515	ACCGACCTGCGCATG[A/C]GGCTGCTGCGCCCGG	84628
rs762343357	snp	A/C			intron-variant, missense	NTNG2	GRCh38.p7	9:132235708	GGTCCCAGGTGGCCT[A/C]CCGTGCAGAAGGTAT	84628
rs762394861	snp	A/C	1.69873e-05	0.00291434	missense	NTNG2	GRCh38.p7	9:132198404	TTCGAGGTGCGGGAC[A/C]GCTTCGCCATCTTTG	84628
rs762414873	snp	A/G	6.91001e-05	0.00587752	synonymous-codon	NTNG2	GRCh38.p7	9:132198322	GTCATCCTCCAGCGC[A/G]CACCGCGTGCTCTGC	84628
rs762426910	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159985	ACTGCTGCCTGCAGG[C/T]TGAATGCTTAAAAAT	84628
rs762455391	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132189285	TTTCTGTAGAGATGG[C/T]ATCTCCCTGTGTTGC	84628
rs762487200	snp	A/C	0.00122556	0.024724	missense	NTNG2	GRCh38.p7	9:132226989	GGCGGGCCGGCTCCT[A/C]CCTGCCGCTGCCCCA	84628
rs762491450	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160692	TCCATTCCCAACACC[C/T]TCTGTGACCTTGGGC	84628
rs762608871	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176103	CCTATAACCCCAGCA[C/T]TTTGGGAGGCCGAGG	84628
rs762648591	snp	C/T	0.000339655	0.0130274	missense	NTNG2	GRCh38.p7	9:132241945	AGAACCAGCGCTGCG[C/T]CTGCCCGCGCGGCTA	84628
rs762664064	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132221895	AAGCCAAGGTCAATG[C/T]TATCACCCAAAGTTG	84628
rs762722526	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182423	TGCACTGGGTTGGCC[A/G]CCTCTCAGCCTAGAG	84628
rs762790177	in-del	-/T	2.41496e-05	0.0034748	frameshift-variant	NTNG2	GRCh38.p7	9:132226863	GGTGCAAGTGCAACC[-/T]GCACGCCAACCTGTG	84628
rs762816539	in-del	-/TT			intron-variant	NTNG2	GRCh38.p7	9:132234028	GAGGTAGAGCTATCT[-/TT]TTTTTTTTTTTTTTT	84628
rs762834902	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132191178	GCTGGCACTCAGTGA[A/T]TGTTACAATCATCAC	84628
rs762840715	snp	A/G/T			intron-variant	NTNG2	GRCh38.p7	9:132225953	CTGTCTTTCCTGTGC[A/G/T]CTCACAGCTGGGTCT	84628
rs762864540	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222841	CCAGTCGCAATGGCT[C/T]ACACCTATAATCCCA	84628
rs762878697	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207678	TTGGCCCACAGCAGG[C/T]ACCTATGACATGCTG	84628
rs762881041	snp	C/T	6.69983e-05	0.00578746	missense	NTNG2	GRCh38.p7	9:132198018	CCAACCCGGACCTGG[C/T]CCACCCGCCCAGGCT	84628
rs762913663	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132227655	TCCTCTACGGCCTGC[A/C]CCAGAGTCCCCCCGC	84628
rs762928212	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201934	ATGAAGAAGCCAAGG[A/G]CTCTGAGGTCAGAGA	84628
rs762966366	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219074	AAAGACACTCTGGCC[A/G]GGTGTGGTGGCACAC	84628
rs762968988	snp	C/T	1.84531e-05	0.00303747	intron-variant	NTNG2	GRCh38.p7	9:132197935	CCGAGCATCCAGCAC[C/T]CACCCTTCCCTTCTC	84628
rs762983913	in-del	-/GG			intron-variant	NTNG2	GRCh38.p7	9:132235558	TTCTAAGGGGCCTGT[-/GG]GGGGTGCGGGGCTGT	84628
rs763004394	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217385	GGTGGCTGCAGTTCC[A/G]GGAGCCTGAGTCTAT	84628
rs763087642	snp	A/G	2.93225e-05	0.00382889	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241051	GCTGCTACCGTGAGT[A/G]CGCGCCGTCCCCCGT	84628
rs763148003	snp	A/G	1.82154e-05	0.00301784	missense	NTNG2	GRCh38.p7	9:132226872	GCAACCTGCACGCCA[A/G]CCTGTGCTCCATGCG	84628
rs763148100	snp	A/C	6.65259e-05	0.00576702	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166781	CCCGCCTGACCCCGT[A/C]GCTGCCTCTCCAGGG	84628
rs763154433	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184646	ACGAGGCCAGAAGCC[A/G]GACATGGTGGCTCAC	84628
rs763163986	snp	C/T	1.81562e-05	0.00301294	intron-variant	NTNG2	GRCh38.p7	9:132198627	AAGGCCGGGGGAAGC[C/T]CTGGATGTCACCTGC	84628
rs763168259	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167396	GCATTCTGGGCGAGT[A/G]AGCAAGATGCTACCT	84628
rs763185817	snp	A/C	3.45608e-05	0.00415683	synonymous-codon	NTNG2	GRCh38.p7	9:132198313	CCGCGACATGTCATC[A/C]TCCAGCGCGCACCGC	84628
rs763227486	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132208180	AGGGAAGGCCCTCCA[A/G]GGAGGGGGGCTTTGA	84628
rs763255655	snp	C/T			missense	NTNG2	GRCh38.p7	9:132198456	TGGACAACCTCTACA[C/T]GCGGCTGGAGAGCGC	84628
rs763362445	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132187318	ACCAGAAAACAAAAC[A/C]GAAAAGCCGCCTTGG	84628
rs763374208	snp	A/C/T			intron-variant	NTNG2	GRCh38.p7	9:132174587	TAAGACGAGACCAGG[A/C/T]GTGTGATGACCTCAG	84628
rs763376478	snp	A/C/T	1.75431e-05	0.00296163	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240871	AAGACGGCGCCCACA[A/C/T]GTAGCCCTGACCGCG	84628
rs763408275	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132225561	AGGTGTGCACCACCA[C/T]GCCTAGCCTGTGTGG	84628
rs763446373	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132215078	TTTTTTGTAGAGATT[G/T]GGGGGGGGGGTCTCA	84628
rs763528399	snp	A/G	3.37524e-05	0.00410793	intron-variant	NTNG2	GRCh38.p7	9:132239051	TCGCCCTGTCCCTCA[A/G]TTTCCCTGAATGCTC	84628
rs763537548	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160709	CTGTGACCTTGGGCT[A/G]GTCTCTCTCTCTCTG	84628
rs763537782	snp	C/T	1.81999e-05	0.00301655	synonymous-codon	NTNG2	GRCh38.p7	9:132226991	CGGGCCGGCTCCTAC[C/T]TGCCGCTGCCCCATG	84628
rs763561515	snp	A/G	0.000185563	0.00963053	intron-variant	NTNG2	GRCh38.p7	9:132238955	GAATCCGATGGAAGG[A/G]TGGGAGGCCTAGGGC	84628
rs763570091	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177908	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	84628
rs763581812	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235585	CTGTGATGCCTCAGT[A/G]TGTACCCAGCTTCCC	84628
rs763600972	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194415	GGGCCATCCCCACAG[C/T]CTCTCAGTCCCTCAC	84628
rs763622474	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132168745	AGGGTTCTCCACACG[C/G]TCTCGGGCACGGTCA	84628
rs763665164	snp	C/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132231763	CTGCCTGGGCCCCCA[C/T]GGCGCCCAGCACCCC	84628
rs763691499	snp	C/T	3.30028e-05	0.00406205	synonymous-codon	NTNG2	GRCh38.p7	9:132166999	GGTGAAGGTGGAGCC[C/T]TCAGGCATCACATGT	84628
rs763698270	snp	A/C/G	0.000241376	0.0109835	missense	NTNG2	GRCh38.p7	9:132241951	AGCGCTGCGCCTGCC[A/C/G]GCGCGGCTACACCGG	84628
rs763735219	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132225965	TGCGCTCACAGCTGG[A/G]TCTAGAGGCTTGATC	84628
rs763764026	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132210470	CCCTTCATCAGTCAA[A/C]AGTCATGCAGGAATG	84628
rs763770304	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182507	TTGCTGTCTCTGCCC[A/G]CTCCAAAATGGAAAA	84628
rs763774252	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132223853	CAGAGCAGGACACGC[C/G]TAACCAGTCAAAGGC	84628
rs763802028	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132222973	AATGAAATTAGCCAG[G/T]CATGGTGGCACGCGA	84628
rs763806556	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175899	GGGAAATCCAGATTG[A/G]TCAGAGACAAAACCA	84628
rs763872871	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132237118	GGGTTACAGAAGTCA[G/T]TTGGAGGATTAATCC	84628
rs763876880	snp	C/T	1.75912e-05	0.00296569	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240863	GGTCCGAGAAGACGG[C/T]GCCCACACGTAGCCC	84628
rs763888321	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132221903	GTCAATGTTATCACC[C/G]AAAGTTGATGGCAAT	84628
rs763965603	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201125	GGGCCCTCATGTCTG[A/G]GCCAGCTGTAGGATC	84628
rs763967313	in-del	-/C	2.06098e-05	0.00321006	intron-variant	NTNG2	GRCh38.p7	9:132227034	CCTGTACGTGCCATG[-/C]CCCGGGGCCACGAGC	84628
rs763969676	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170187	GGGGTGCAGACCCTC[C/T]CTCTTTCCCAGGCTT	84628
rs764007569	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132201718	CGAGCATTTGCTACG[G/T]GCTCATTTGCTATTG	84628
rs764034257	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132238583	GCGTTTTCCTCCCAG[A/C]CATCTTCCAAAGCAG	84628
rs764053255	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132228485	CTCACAAATTTGCTG[C/T]CCTTTCGTCTGTCCT	84628
rs764094013	in-del	-/ATTC			intron-variant	NTNG2	GRCh38.p7	9:132211917	ATATGTGTGGAATTC[-/ATTC]ATTCATTCATTCAGT	84628
rs764097032	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132203747	GCCAACACACTGGAG[C/G]CAGGGCAGGGGCAAG	84628
rs764104122	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132167399	TTCTGGGCGAGTGAG[C/G]AAGATGCTACCTGCA	84628
rs764192239	snp	C/T			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166648	CTGAATTTTCCGTGT[C/T]GGCCTTTTGGAAACA	84628
rs764202136	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199073	TAGGGACTGCCTAGG[A/G]TGGCTGGGGCTGCAC	84628
rs764250771	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207731	CCAAGAGCATGGAGG[A/G]GCTGACGCTCCCGTA	84628
rs764264307	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132234199	ATGTTCAGCTACTTT[A/T]TGTCTTTTTAGAGAG	84628
rs764266870	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132179898	CTGGGATCTCACTGG[G/T]CGGCCACAGAGGGGT	84628
rs764274186	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132197159	CTTTGGGAGGGCAAG[A/C]CAGGTGGATCAACGG	84628
rs764292175	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132208207	TTGAAGGAGAAACCT[C/G]AAGGGGGAACGGGGG	84628
rs764329558	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132221259	GGCAGAGGGAACAGC[A/G]TGTGCAAAGGCCCAG	84628
rs764331308	in-del	-/GTTTTT			intron-variant	NTNG2	GRCh38.p7	9:132195308	CTTTTTTTTGTTTTC[-/GTTTTT]GTTTTTGTTTTTTGA	84628
rs764353349	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213825	GGTACCAGAGCTCTG[C/T]GAGGCCAGTCTCAGT	84628
rs764391082	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132186521	TCATTCAGGGGTCTG[A/C]GGTCCTGATGAGCAG	84628
rs764457747	snp	C/G			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244035	CTGGGGCTTCTTGTG[C/G]ATAGGAGTGGCCAGG	84628
rs764474048	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208907	GCCCCCATCCTGCTC[C/T]CTGAAAATCTGCTGT	84628
rs764510257	snp	C/G	1.76353e-05	0.0029694	intron-variant	NTNG2	GRCh38.p7	9:132241828	GAGCTCGGAGGTTGG[C/G]GGGGGGACCGGGCCA	84628
rs764521654	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132226125	GGACTGCAAATTCTC[-/T]CGTGAAATGCTTCTA	84628
rs764535959	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205081	GCTCCTGAACAAGTT[A/G]CATGTAGATTTAGCA	84628
rs764540838	snp	A/C	5.18551e-05	0.00509165	missense	NTNG2	GRCh38.p7	9:132198319	CATGTCATCCTCCAG[A/C]GCGCACCGCGTGCTC	84628
rs764547540	snp	A/G	1.69198e-05	0.00290854	missense	NTNG2	GRCh38.p7	9:132198224	AAGTCCCTGGACAAC[A/G]GGCGCACCTGGCAGC	84628
rs764627140	in-del	-/AGG	1.66324e-05	0.00288374	cds-indel	NTNG2	GRCh38.p7	9:132198045	GGCTCATGTTCGACA[-/AGG]AGGAGGAGGGCCTGG	84628
rs764637800	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132224924	TGTATCTCTCTCTGC[-/T]TTTTTTTTTTCCTTT	84628
rs764648471	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230923	TGCAGGTCTCTTGGC[C/T]CCTGGGTGGGCTCCC	84628
rs764655545	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160040	CTCCCAAGGAGCTTC[C/T]TCCTGCATAGAACAG	84628
rs764660488	snp	A/C			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159924	AGGCTGAGGGCTGAC[A/C]CTGGTCATCACTCAC	84628
rs764664190	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204377	CTGTCCCTATTGATC[A/G]CCCCGTAACTGGAGA	84628
rs764665228	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176106	ATAACCCCAGCACTT[C/T]GGGAGGCCGAGGCAG	84628
rs764668208	snp	A/G	5.92786e-05	0.00544388	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241087	GGGCCTGCGGAAAGG[A/G]GACGGGGCAGGACCG	84628
rs764703217	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132215079	TTTTTGTAGAGATTG[C/G]GGGGGGGGGTCTCAC	84628
rs764736408	snp	C/T	1.67761e-05	0.00289617	intron-variant	NTNG2	GRCh38.p7	9:132239066	GTTTCCCTGAATGCT[C/T]GCTGACCATTGGTAT	84628
rs764789317	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132206400	GGCCGGGCGTGGTGG[C/T]TCACGCCTGTAATCC	84628
rs764801164	snp	A/G	0.000104608	0.00723139	synonymous-codon, missense	NTNG2	GRCh38.p7	9:132241937	CTGCCTGCAGAACCA[A/G]CGCTGCGCCTGCCCG	84628
rs764822028	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187516	GAGGGACAGCGATCA[A/G]TGAAACCATAGAAGG	84628
rs764857818	snp	C/T	3.46105e-05	0.00415981	synonymous-codon	NTNG2	GRCh38.p7	9:132198301	CGCCCGCCGGGCCCG[C/T]GACATGTCATCCTCC	84628
rs764876422	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132220855	TCTTTTTACGTGGGT[A/C]TCCCATATTATTTAT	84628
rs764877198	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132208352	AGATCACGCCAGCCC[-/T]GCAGCCCCGGGAGGA	84628
rs764893748	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239884	AGCCCAGGTCCAGCT[A/G]TAAAGCTGCTCTTCA	84628
rs764925509	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132194267	GGAGCATCTGCCCAT[A/C]ACTCCTCCTCCCGAG	84628
rs764944956	snp	A/G			intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231662	CAGCAGGTCCCAGAA[A/G]GACCCCGACCCCAAA	84628
rs764965433	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180221	GACCAGGCATTTTCC[C/T]TTGGCCGAAGCAGAA	84628
rs764980946	snp	C/T			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166669	TTTGGAAACAACAAG[C/T]TCCTCGCTGTTTGCA	84628
rs765095306	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235995	ATGTGGCACCCCCAC[A/G]CCAAGCCCTTCCACC	84628
rs765125921	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132210262	ACCTGTAAAATGGGA[A/T]CCCGCTCTTGTAAAG	84628
rs765155501	snp	A/G	1.6495e-05	0.0028718	synonymous-codon	NTNG2	GRCh38.p7	9:132166987	GGACTACGTCAAGGT[A/G]AAGGTGGAGCCCTCA	84628
rs765172585	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168392	TGGTGGGGCTGACCC[A/G]GTGCCCCCACCTCAG	84628
rs765175565	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236879	GAGTGGGACTCCAGG[A/G]ACAGCGAAGGATTCA	84628
rs765246278	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132236558	CGAGCAGGGCTTTGA[G/T]CGCCCTCTACTGGCA	84628
rs765299076	in-del	-/TTTG			intron-variant	NTNG2	GRCh38.p7	9:132225251	TGTTTTTGTTTTTGT[-/TTTG]TTTGTTTTTGTTTTG	84628
rs765300602	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132223693	AAAAGATGCCGCACA[A/C]CCCAGGCGGGACGGG	84628
rs765317291	snp	A/G	1.80172e-05	0.00300138	synonymous-codon	NTNG2	GRCh38.p7	9:132226978	CACCCGGTCCTGGCG[A/G]GCCGGCTCCTACCTG	84628
rs765317326	snp	C/T	1.64868e-05	0.00287109	synonymous-codon	NTNG2	GRCh38.p7	9:132166897	GGACTATGACATCTG[C/T]AAATCCTGGGTGACC	84628
rs765330342	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132234142	CAAGCAATTCTCCTG[C/G]CTCAGCCTCCCGAGT	84628
rs765347293	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218113	GCAGGCCACACAGCT[A/G]TGTGCACCATGAGCT	84628
rs765417352	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132219035	ATCACCACAGCAGAC[G/T]TTAGAACATTTCCAT	84628
rs765426029	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217120	CCTGGCCCTTGACCC[A/G]TCTGAGCCTCGCATT	84628
rs765479199	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181979	GTGTGTGTGTGCGTG[C/T]GTGCAGCCATGTGTG	84628
rs765495779	snp	C/T	6.83118e-05	0.00584391	synonymous-codon	NTNG2	GRCh38.p7	9:132198547	GCTGGGCGGCACCTA[C/T]GTGCAGCGGGAGAAC	84628
rs765511616	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132197196	GAGTTCGAGACCAGC[C/G]TGGCCAACATGGCGA	84628
rs765519680	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184329	GGAACACCTGGAGAG[A/G]GAAGGGGCCGAGGAG	84628
rs765542111	snp	C/G	1.6571e-05	0.0028784	missense	NTNG2	GRCh38.p7	9:132198088	GCAGAGCATCACCTG[C/G]AGCCGCTACCCCAGC	84628
rs765572045	snp	C/T	1.67464e-05	0.0028936	synonymous-codon	NTNG2	GRCh38.p7	9:132198190	CGAGTACGGCCGGCC[C/T]ACGGTCATGGTCCTG	84628
rs765612093	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132176176	CAATGTAGTGAGACC[C/G]CATCTCTCAAAAAAA	84628
rs765705117	snp	A/C			missense	NTNG2	GRCh38.p7	9:132198326	TCCTCCAGCGCGCAC[A/C]GCGTGCTCTGCACCG	84628
rs765707795	snp	C/G	0.000325256	0.0127484	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231320	CCCTCCCCCTGGGAG[C/G]TCGCCATCTGCTCTG	84628
rs765732125	snp	C/G	0.000154989	0.00880174	synonymous-codon	NTNG2	GRCh38.p7	9:132198334	CGCGCACCGCGTGCT[C/G]TGCACCGAGGAGTAC	84628
rs765782038	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212753	ATGAATTAGCTAGAA[A/G]TGCAGTTTGCTACCA	84628
rs765782093	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132225461	TTTCTGTAGAAACAG[G/T]ATCTTACTATGTTAC	84628
rs765789610	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212568	GCCAGGCTGCGCCAG[A/G]CGACCAACCCAGACC	84628
rs765821013	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132172331	TTACTGACTGGCCTA[C/T]CAGTGAAGAGTTCTG	84628
rs765834491	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132186030	CTCCTTTTTCTAATC[A/T]ATTAGAAAGTGTTTA	84628
rs765909194	snp	A/G	1.66338e-05	0.00288386	synonymous-codon	NTNG2	GRCh38.p7	9:132198163	GCTGACCGACGACGT[A/G]GTGATGACCTTCGAG	84628
rs765974149	snp	C/G	1.93186e-05	0.00310788	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240980	CTGCGAGTGCCGCGA[C/G]GGCGCGGCGGGCCCC	84628
rs766004190	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204261	GCTTCCCCAGACCCT[A/G]TGGGGGTCTAGCTGC	84628
rs766011992	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229870	TGATGAATCTCACCC[A/G]GGGATTTCAAGGCCC	84628
rs766024770	snp	C/T	1.64931e-05	0.00287163	missense	NTNG2	GRCh38.p7	9:132166877	TGCCTCCCTCTGGCC[C/T]CTGGGGACTATGACA	84628
rs766052613	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204771	AGGAAACTGAGGCCA[A/G]GAGGTTGAGATATAG	84628
rs766052644	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230103	CCTGGCACGTGGGAC[A/G]CACTCCACCCGCGGC	84628
rs766066086	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239712	CCTCCTGCAGGGGCC[C/T]AGTTGGGGGCCAAAA	84628
rs766072662	snp	A/G	1.66161e-05	0.00288232	synonymous-codon	NTNG2	GRCh38.p7	9:132198049	CATGTTCGACAAGGA[A/G]GAGGAGGGCCTGGCC	84628
rs766154615	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219344	TTGGGAGGCCCAACT[A/G]GGAGGATCACTTGAG	84628
rs766198754	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167673	GCCCCTGGGTAAGTC[A/G]GGGGAAGGCAGACAT	84628
rs766301826	snp	C/G			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166382	CGTTGTGTTGAGCAC[C/G]TCACCCATTAAGAGC	84628
rs766302889	snp	G/T	1.71006e-05	0.00292404	missense	NTNG2	GRCh38.p7	9:132198534	TGCTGCGCCCGGCGC[G/T]GGGCGGCACCTATGT	84628
rs766349111	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132220429	ATTGCTTAATTCAAG[A/G]TCATGAAGATTTGCT	84628
rs766356969	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132187327	CAAAACAGAAAAGCC[A/G]CCTTGGCCAGCTGCA	84628
rs766368510	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235121	GCCAGGGGTCAGGAA[A/G]GTAGAAGGGCAGTGA	84628
rs766440510	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132241644	AAGAACAGCACCGAG[G/T]CCAGTGGGGCGGGGA	84628
rs766447551	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132188584	AGCGTGGGAGGTGGG[G/T]TTGAGGCACACAGGG	84628
rs766458760	snp	A/G	1.7141e-05	0.0029275	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241068	GCGCCGTCCCCCGTG[A/G]GCGGGGCCTGCGGAA	84628
rs766504033	snp	A/G	3.39035e-05	0.00411711	missense	NTNG2	GRCh38.p7	9:132198428	ATCTTTGCCGGCCCC[A/G]ACCTGCGCAACATGG	84628
rs766594004	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132235950	GGTCTACCAGCTCTG[A/C]CCCCAAGCTCACCTG	84628
rs766629967	snp	C/T	4.98832e-05	0.00499391	synonymous-codon	NTNG2	GRCh38.p7	9:132239234	GGGCTACTACCGCAA[C/T]GGCTCGGCAGAGCTG	84628
rs766663146	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196094	GAACCATTGTTGATA[C/T]ATTATTATTAACTAA	84628
rs766668199	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132217972	GTGGGTGATGTGGCC[A/G]GTGTGGTCCATATCG	84628
rs766668246	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205917	GTGATAAATATATAC[A/G]TATATTTTAGCACAC	84628
rs766727877	snp	C/T	0.00016707	0.00913823	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231255	CATCGAGACTGTCCC[C/T]AGACACTCACAGGGT	84628
rs766825272	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132214641	CAAGCAAGTGAGTGC[A/G]CCCCATGTCAGGCCG	84628
rs766859521	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132206725	ACACCCAGCTCTTTG[C/G]GGACAGACATTTTGT	84628
rs766943307	in-del	-/AGA			intron-variant	NTNG2	GRCh38.p7	9:132194159	GTCCCCAGGGGCAGC[-/AGA]AGCAGCACTGGGACT	84628
rs766954267	snp	C/T	7.25452e-05	0.00602224	intron-variant	NTNG2	GRCh38.p7	9:132197952	ACCCTTCCCTTCTCC[C/T]CTCCCCGCTGCAGGA	84628
rs766974228	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132197022	TCACAGAGTAAGGGA[A/T]CGGGGAGAGACCCAG	84628
rs766982407	snp	C/T	3.33322e-05	0.00408228	missense	NTNG2	GRCh38.p7	9:132198032	GCCCACCCGCCCAGG[C/T]TCATGTTCGACAAGG	84628
rs766999337	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168850	GGGAGCAGCTAAATC[A/G]TAATTCTAGGACCAG	84628
rs767002297	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191602	AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	84628
rs767007316	in-del	-/AAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213333	TAAGACTCCATCTCA[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84628
rs767016356	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196941	GAACAGCTCACGGAA[C/T]TCAGAAAGGCATTTT	84628
rs767135849	in-del	-/CTT			intron-variant	NTNG2	GRCh38.p7	9:132166165	GCAGAACCAAATAGC[-/CTT]CTCCCCAGTGAACAC	84628
rs767196156	snp	A/C	4.96882e-05	0.00498414	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230535	CCCAGGCCCCTTCCC[A/C]TGGGGCAGCCAGCTC	84628
rs767206567	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191434	CAATCAATAAGAAAA[C/T]AGAGACTCAGAGAAG	84628
rs767207886	snp	A/G	1.82217e-05	0.00301837	intron-variant	NTNG2	GRCh38.p7	9:132198630	GCCGGGGGAAGCCCT[A/G]GATGTCACCTGCAAC	84628
rs767233239	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212458	AGGGCTTCGCACAGA[A/G]GCCCAAATTTGATTT	84628
rs767321328	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211677	TGGCTCAGAGAGCAC[C/T]TCTCTGGAGCTCCTG	84628
rs767336343	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132178435	GATAATTATCCATCA[C/T]TTCAAATAGAGACAC	84628
rs767354512	snp	C/T	1.70592e-05	0.0029205	missense	NTNG2	GRCh38.p7	9:132198563	GTGCAGCGGGAGAAC[C/T]TCTACAAGTACTTCT	84628
rs767425690	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202713	AACCATTAAGAGAAG[C/T]GGGGCCCAAACCTGA	84628
rs767598082	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132215319	GGCATGGTGGCTTAT[A/T]CCTGTAATCCCAGCA	84628
rs767646738	snp	C/G	1.67273e-05	0.00289195	intron-variant	NTNG2	GRCh38.p7	9:132239070	CCCTGAATGCTCGCT[C/G]ACCATTGGTATTTCT	84628
rs767670551	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132235868	AACCAACTGAGGGCA[C/T]GGGTGTAGAATGTCG	84628
rs767682319	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132178460	AGACACACAACTTAG[A/T]AGGCATGCTGGGATT	84628
rs767699508	snp	C/G	1.72537e-05	0.0029371	missense	NTNG2	GRCh38.p7	9:132198325	ATCCTCCAGCGCGCA[C/G]CGCGTGCTCTGCACC	84628
rs767748378	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132225856	TCTGTTGGAAGAAGT[-/G]GGTCATTACTGCCGG	84628
rs767777100	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227364	TCCAGCCCTGGTCCA[C/T]AGGGAAACCCGAGAG	84628
rs767868543	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232633	GGGCACCAGGAAGAC[A/G]ATGACCAAGGGGAAT	84628
rs767869114	snp	A/G	1.78242e-05	0.00298526	missense	NTNG2	GRCh38.p7	9:132241957	GCGCCTGCCCGCGCG[A/G]CTACACCGGCGTGCG	84628
rs767904300	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226179	ACTTTCGGTTACCCC[A/G]AGGTACAGTTTATAT	84628
rs768026072	in-del	-/TGTC			intron-variant	NTNG2	GRCh38.p7	9:132216467	GTGTGTGTGTGTGTG[-/TGTC]CCATGGAGCGTTCTT	84628
rs768080401	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132231871	TCTCTTGGGGTGGGA[A/G]GGTCGGCAGCCCTGG	84628
rs768116983	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132214348	CCCAGGCACTGCCTG[A/C]CCCTCCCTGCAGCGC	84628
rs768137421	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132164233	TTTTAAATTTATTTA[C/T]TTTCCAGGGAATGCG	84628
rs768140427	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132191360	CAAAATAATCGCTCC[C/T]ATTTGGAGACATTTC	84628
rs768161075	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205816	AACCAGGGAAGTGGA[A/G]GTTGCAGTGAACTGA	84628
rs768180851	snp	C/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244988	CAGCACTGTTCTTGT[C/T]TGGAGGCAAGTGGGC	84628
rs768267533	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132196687	TCACACCAAATGTAT[A/G]GGTTTTCCACACCAA	84628
rs768357432	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132206448	GAGGCAGGTCCATCA[C/G]CTGAGGTCAGGAGTT	84628
rs768358859	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183557	CCCAGCCCGTCACCT[C/T]CAGGGCTTGTCATCT	84628
rs768390365	in-del	-/AGC			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160238	GAAACTGAGCCCCAA[-/AGC]AGTCTGGGCCGTGTT	84628
rs768411685	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132232549	TCTCACCTGGACTCA[C/G]CTGGGGAGTATCCCT	84628
rs768469840	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197550	CAAAGGCTCAGAGGT[A/G]CAACCAGGCAGGGGC	84628
rs768480508	snp	C/T	1.69922e-05	0.00291476	synonymous-codon	NTNG2	GRCh38.p7	9:132198505	CTTCACCCTCACCGA[C/T]CTGCGCATGCGGCTG	84628
rs768526201	snp	C/T	0.000311187	0.0124698	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231429	TGCACCGTCACCCTC[C/T]ACCAGGGCTCTGTGG	84628
rs768532535	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193592	GTGACGCCACTTGGT[A/G]CCAGCGTACTGAGAA	84628
rs768602899	snp	C/T	1.67245e-05	0.00289171	synonymous-codon	NTNG2	GRCh38.p7	9:132198022	CCCGGACCTGGCCCA[C/T]CCGCCCAGGCTCATG	84628
rs768661353	snp	C/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160299	AGAGAGCATCACCCA[C/G]AAACCCAAAAGCCCT	84628
rs768667250	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227734	GAGCCATCCTCAGGG[C/T]CTGCCCACTCACATC	84628
rs768694924	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213253	CTTGAACTTGGGAGG[C/T]GGAGGTTAAAGTGAG	84628
rs768808771	snp	C/T	7.72708e-05	0.00621526	intron-variant	NTNG2	GRCh38.p7	9:132241864	CGTGCTGACCGCCCC[C/T]TCCGCCTGCAGCCAA	84628
rs768847860	in-del	-/CT			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165995	GTTGTTGCTAATGAG[-/CT]CTCTCTCTCTCTCCT	84628
rs768862872	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168061	ACAGAGTAAGTGCAC[A/G]CAGATGTTAGCCGTT	84628
rs768871605	snp	G/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209317	TTTTGGACCTGTTGG[G/T]TGTGAGCGTTTTGGA	84628
rs768920815	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132181909	GCTGCTCAGCTGACA[C/G]GAGTCGCTCTGGATC	84628
rs768936060	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167786	CAGCAACAACAACAG[C/T]AGAGATGGTTGCGTG	84628
rs768958528	snp	C/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132235710	TCCCAGGTGGCCTCC[C/T]GTGCAGAAGGTATGG	84628
rs768971545	snp	C/T	3.63848e-05	0.0042651	synonymous-codon	NTNG2	GRCh38.p7	9:132226874	AACCTGCACGCCAAC[C/T]TGTGCTCCATGCGCG	84628
rs769061259	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132169734	CGGCACAGCCCGGCC[A/G]TGCTGCCGTGGTACG	84628
rs769073297	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132199222	CTGGTGCTGACTGTG[A/G]GAAGTGCTCTGAGGC	84628
rs769075099	snp	A/G	5.10096e-05	0.00504997	missense	NTNG2	GRCh38.p7	9:132198399	TGCGCTTCGAGGTGC[A/G]GGACCGCTTCGCCAT	84628
rs769099112	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201538	CTGGTGGCAAAGGGG[A/G]ATGTGGGACCCGAAG	84628
rs769117760	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132236521	ACATGTTCAAATTTC[C/T]TCCAGCCCCAGCTCT	84628
rs769123740	snp	C/T	1.6955e-05	0.00291157	missense	NTNG2	GRCh38.p7	9:132198495	TCAAGGAGTTCTTCA[C/T]CCTCACCGACCTGCG	84628
rs769163155	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201355	AGGTGGTGGCGAGAG[C/T]GTACAATCAATTCAG	84628
rs769163722	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179945	GTCTCGTTGGCAGGA[A/G]GGAATTGTATTGGAA	84628
rs769278565	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132175937	CAGTGGACTCCAGTG[C/T]AGACAGAGGGGTCCT	84628
rs769307236	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132210719	GGGAAGTTGAGTGGG[A/G]AGAGGACAGGCCACA	84628
rs769308545	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132227078	ATCTTCCCTGCCCGT[C/G]AATCCCAGGAGCTGT	84628
rs769317415	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132194634	GCTGGGGCCAGTCCT[-/AC]CCTGGCCCGGGCCTC	84628
rs769317562	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176570	CTGTGGACACACCAT[A/G]TTTTGTGTATCCGTT	84628
rs769344644	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188158	CCCCACGATTGCTTC[C/T]CCCGTGCTCGAGTCC	84628
rs769374475	snp	A/T	3.41082e-05	0.00412952	missense	NTNG2	GRCh38.p7	9:132198381	CCAAGAAGGAGAAGC[A/T]CGTGCGCTTCGAGGT	84628
rs769384672	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132177748	CTGCAACCTCCCCCT[C/G]CCGGGTTCAAGCGAT	84628
rs769531651	snp	C/T	3.30748e-05	0.00406649	synonymous-codon	NTNG2	GRCh38.p7	9:132239123	CGAATGCTACGGTCA[C/T]TCCAACCGCTGCAGC	84628
rs769569830	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132223615	ACGGAAGTTGCAGTG[A/T]GCCAAGATTGTGCCA	84628
rs769570116	in-del	-/GTGT			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162571	AGAGAGAGACAGAGT[-/GTGT]GTGTGTGTGTGTGTG	84628
rs769574977	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196582	CCTAAAAATGCCCTG[C/T]GCTCGGCCTAGTCAT	84628
rs769584402	snp	A/C			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243881	TGCTCCCACCCCCAG[A/C]ACCCTGCTGACCCGG	84628
rs769642682	in-del	-/CCTT			intron-variant	NTNG2	GRCh38.p7	9:132189063	GAAAAAGGCTTTAAG[-/CCTT]TCTTTTTTTTTTTTT	84628
rs769651898	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182202	AGCTCTGGGGAAGGC[A/G]AGATGGCTTTGCCTG	84628
rs769671964	snp	G/T	0.000130591	0.00807951	synonymous-codon, missense	NTNG2	GRCh38.p7	9:132242033	GGACTGCGACCGCGC[G/T]CCCGGGGCCGCCCCG	84628
rs769677510	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170233	GGCCACCTGAGAACT[A/G]AATTGTAAATTCCAG	84628
rs769688617	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211519	TCTCACCTCCTTCTG[C/T]AGCCTGGGCTCTGAG	84628
rs769690612	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132232272	CCTCAGCAGCACACC[G/T]GTGGGATGGATGGAG	84628
rs769704763	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132192037	CTAGAGGTGTGCCTA[A/G]CAGTCTCTCCCTATA	84628
rs769739666	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229627	CTGTGGCTGCACCCC[A/G]AGGTGTCCTCAGGGT	84628
rs769782655	snp	G/T			synonymous-codon	NTNG2	GRCh38.p7	9:132226864	GTGCAAGTGCAACCT[G/T]CACGCCAACCTGTGC	84628
rs769797063	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203479	CAGCAGGCGCCTCAC[A/G]AGACAGTGGACCAAA	84628
rs769808940	snp	A/G/T			intron-variant	NTNG2	GRCh38.p7	9:132222832	GACTTTAGGCCAGTC[A/G/T]CAATGGCTCACACCT	84628
rs769842414	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240506	CAAAGGAGCTATGGA[A/G]GGGGGCCACCCCACA	84628
rs769847330	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132183430	TTGTGTGTCCAGCCT[A/G]GCCCTTTGCTCAGTC	84628
rs769865279	snp	A/G			missense	NTNG2	GRCh38.p7	9:132239241	TACCGCAACGGCTCG[A/G]CAGAGCTGGATGATG	84628
rs769881263	snp	A/C	2.81179e-05	0.00374942	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241044	CGCCAGGGCTGCTAC[A/C]GTGAGTGCGCGCCGT	84628
rs769918722	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233210	ACAGTGGTGGTGGGT[A/G]CTGTGCCTGTCTCCA	84628
rs769989641	snp	C/T	1.70087e-05	0.00291617	intron-variant	NTNG2	GRCh38.p7	9:132239041	GAGTCCTTCCTCGCC[C/T]TGTCCCTCAGTTTCC	84628
rs769999122	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132179796	GCCAAAACTAGGATC[C/G]GTCTCCAGGGCCTCC	84628
rs770011075	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132220051	TGAGTGTGAAGTGGT[A/G]TCTCATTATGGCTTT	84628
rs770031976	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132233334	CACACGCACATGTAC[-/AC]ACACACACACACACA	84628
rs770040093	snp	A/G/T	3.52089e-05	0.00419565	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240946	GCTCCGTGCACGACC[A/G/T]GTGCAACGAGACCGG	84628
rs770061739	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132221420	ATGTCCACACACACC[A/G]ACACAGAGGCAGTAC	84628
rs770079467	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167984	AGCACACACTCCTAG[A/G]GTCATTGTGAGGAGT	84628
rs770102416	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132165701	ACAGTCATGGTATTT[C/T]AAAGCAACCATTAAA	84628
rs770167332	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180534	CTCAGCTCCTAGGGA[C/T]GGGGCTCCCCCAGGC	84628
rs770168260	snp	A/G	1.64866e-05	0.00287106	missense	NTNG2	GRCh38.p7	9:132166955	TACGCCTGCCAGCCC[A/G]AGGTGATGCGCCTGA	84628
rs770199234	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132208027	GAGGATTGCTTGAGC[C/G]CAGGAAGTCAAGCCT	84628
rs770204907	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196936	TGCTAGAACAGCTCA[C/T]GGAACTCAGAAAGGC	84628
rs770286055	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132222886	TGAGGTGGGCAGATT[A/G]CTTGAACTTCAACCA	84628
rs770344563	in-del	-/AGCCGTTAA			intron-variant	NTNG2	GRCh38.p7	9:132173208	CACCTGAGCTGCACC[-/AGCCGTTAA]AGCCACTCAGTCTCT	84628
rs770369982	snp	C/G	1.73333e-05	0.00294386	missense	NTNG2	GRCh38.p7	9:132198294	GTATGTCCGCCCGCC[C/G]GGCCCGCGACATGTC	84628
rs770441740	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132214596	GGTGGCTGTGGCTCT[C/G]TCCTTGCTGGCAGCA	84628
rs770502510	in-del	-/AA	1.91298e-05	0.00309266	intron-variant	NTNG2	GRCh38.p7	9:132197921	TTCCCAGGCCATCCC[-/AA]GAGCATCCAGCACCC	84628
rs770514163	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132167932	CAGTGACGTCTGTGG[C/G]CTTCTGTTCTGTCAT	84628
rs770549848	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132231796	AGCCCACAGGTGGGT[A/G]CCAGGGTACAGCGAC	84628
rs770562092	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174238	GACAGACAGGCAGGC[C/T]GCACCATGCTGTGGA	84628
rs770602742	in-del	-/AGAC			intron-variant	NTNG2	GRCh38.p7	9:132192774	GGGGGACAAGGAGAA[-/AGAC]AGAAAGAGAAAGAGG	84628
rs770668434	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160351	AGCTATGTGACCTTG[A/G]GCAAGTTACTTAACA	84628
rs770685056	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162566	TGTGTGAGAGAGAGA[C/G]AGAGTGTGTGTGTGT	84628
rs770695615	snp	A/G	1.77175e-05	0.00297631	missense	NTNG2	GRCh38.p7	9:132226968	AGAATTTCCGCACCC[A/G]GTCCTGGCGGGCCGG	84628
rs770734148	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132188793	AGCCAGTGCTAGTAA[A/C]CTCATTGAGCGTTCA	84628
rs770760028	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159755	CAGTGCTAGGGAGGA[A/G]GCACCCCTGGTTCCT	84628
rs770780900	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132233693	CCCCATTAATGAAAA[C/T]GATCATTGCAGTAGC	84628
rs770784512	snp	A/C/G	0.000351818	0.0132593	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132242004	TGCGACCCCGCCGAC[A/C/G]ATGACGGCGGTCTGG	84628
rs770823053	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243593	GCAGTGCCGGGGGTC[C/T]GGTCCTGGTTGCTAA	84628
rs770859227	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132221672	GGAAGACAGGACTGA[C/T]AGGAGGGGCTGGCCA	84628
rs770872322	snp	G/T	5.97425e-05	0.00546513	synonymous-codon, missense	NTNG2	GRCh38.p7	9:132241883	GCCTGCAGCCAACGT[G/T]TGCGACGACGACCAG	84628
rs770872552	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132210392	CACACAGACCATGTT[C/T]CTCCGTCACTCGCCT	84628
rs770890788	in-del	-/TTTTTTTTTTTT			intron-variant	NTNG2	GRCh38.p7	9:132189072	CTTTAAGCCTTTCTT[-/TTTTTTTTTTTT]TTTTTTTTTTTTTAG	84628
rs770925728	snp	A/G	1.70834e-05	0.00292257	synonymous-codon	NTNG2	GRCh38.p7	9:132198373	GGCAGGCTCCAAGAA[A/G]GAGAAGCACGTGCGC	84628
rs770933895	snp	C/T	1.75001e-05	0.002958	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240935	CAACCAGATAGGCTC[C/T]GTGCACGACCGGTGC	84628
rs771045958	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194073	CTGTCTCCAAATACA[A/G]TCCCATTCTCAGATA	84628
rs771118877	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229451	AGCAGCCCTCACTCC[C/T]GATGCCTTCCCACCT	84628
rs771130953	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132179632	GCTTCCGTAGTGCCA[A/T]GCACCGGTGGCAATT	84628
rs771153100	snp	A/C/G	3.3052e-05	0.00406511	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166828	CTCTGCAGACTGCGC[A/C/G]GCCATGCTGCATCTG	84628
rs771183049	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132171112	CCAAGGCGGGGGGTC[A/T]GTGCTTCTGAGCAGG	84628
rs771185910	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162824	TTCTCCCGGCGCCGG[A/G]AGGGGGTCGGGAGGT	84628
rs771200638	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203422	TACCTATGGTACCAG[C/T]GGAAGCGATAGGGAA	84628
rs771203654	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202463	CGCAAGTCCCAGCCA[C/T]GCCCCCTCCCTGCCT	84628
rs771205510	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227398	CTGCTCAGCAGCATT[C/T]CTGCAACCCTTCGCC	84628
rs771238859	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132183934	CCAGGAATGTTGCCA[C/G]ACCCCTCCCGTCCCC	84628
rs771279004	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229202	TGCTGTCCTCAGCAC[A/C]CAAGTCTCCTGCCTT	84628
rs771325031	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167175	CCTCTTGACCAGGTC[C/T]GGACCAGACCTGGAC	84628
rs771334327	snp	A/G	1.68627e-05	0.00290363	missense	NTNG2	GRCh38.p7	9:132197999	AGCAACGAGTGTGAC[A/G]CCTCCAACCCGGACC	84628
rs771349575	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132216761	ATTGATCCCACAGAA[G/T]AAGGGGAAATATCTG	84628
rs771390002	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234763	CATGGCTCTAATTAA[A/G]CCCTTGCCAATTTGG	84628
rs771401037	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132165368	AGCACAGCAATAATC[A/G]TAATTGTAACCCATT	84628
rs771436115	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132218960	TCACACGTTGTACAA[A/T]CCACACATGTAAAGC	84628
rs771476804	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240025	GACCGCCAACCAAAA[C/T]GCACCAGCCTGGAAT	84628
rs771490001	snp	A/G	1.6775e-05	0.00289607	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241030	CCACGCACTACTGGC[A/G]CCAGGGCTGCTACCG	84628
rs771502294	snp	C/T	0.0012747	0.0252136	intron-variant, missense	NTNG2	GRCh38.p7	9:132231512	GGGAAGCCAGTGAGC[C/T]GAGAGGGCGCCAGAA	84628
rs771529834	snp	C/T	1.79309e-05	0.00299419	intron-variant	NTNG2	GRCh38.p7	9:132198617	ATCGGCAGGTAAGGC[C/T]GGGGGAAGCCCTGGA	84628
rs771544626	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207992	GCCTGTGGTCTCAGA[C/T]ACCTGGGAGGCTGAG	84628
rs771580338	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132224803	TGGTGTCTGCCATGA[C/T]GAACCTCTGTGTACC	84628
rs771585135	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233586	AGGACATTAGGGGAG[A/G]AGGTGGCTCCAATGT	84628
rs771590912	in-del	-/GT			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162536	GTCGTGTGTGTGAGA[-/GT]GTGTGTGTGTGTGTG	84628
rs771594145	in-del	-/AACT			intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162664	TGTCTCGGAAAAGGA[-/AACT]AACCCTGCTCCCGCG	84628
rs771630644	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132207462	GCTGTCCGCTCCCTG[A/C]GCATCTGTCTTACAC	84628
rs771684404	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234586	AGCTGGGCCTCTGAA[C/T]TCCTGGGCCAGATGT	84628
rs771788973	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132172154	TCCTCCACCCGAATG[C/G]CTGCCCCCTCCTTCC	84628
rs771790422	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173623	TCCAATCCCACCTGC[A/G]ATGGGGCAGGCAGTG	84628
rs771801621	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223822	TGAAGCAGCCACAGC[A/G]TTATAAAATATGGCC	84628
rs771867546	in-del	-/CTT			intron-variant	NTNG2	GRCh38.p7	9:132193970	CATCCGGCAGCCAAA[-/CTT]CTTCTTCTTCCAAGG	84628
rs771895616	snp	A/G	0.000124883	0.007901	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241055	CTACCGTGAGTGCGC[A/G]CCGTCCCCCGTGGGC	84628
rs771927209	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230334	GTCTCCTTCTGCAAA[A/G]TGGGCCAATAGTGGT	84628
rs771958614	snp	A/G	1.65919e-05	0.00288022	missense	NTNG2	GRCh38.p7	9:132198140	CTTTCGTGGAACAAG[A/G]CCGTGGAGCTGACCG	84628
rs771959282	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229956	CTGGATTCAGGTCAG[C/G]CCTCGCCCACTCTCG	84628
rs772018282	snp	C/T	5.20983e-05	0.00510357	missense	NTNG2	GRCh38.p7	9:132198290	TTCGGTATGTCCGCC[C/T]GCCGGGCCCGCGACA	84628
rs772024264	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132192790	GACAGAAAGAGAAAG[A/G]GGGAGAGAGAAAATT	84628
rs772049471	in-del	-/AAA			intron-variant	NTNG2	GRCh38.p7	9:132219573	GCAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAGA	84628
rs772095252	in-del	-/TTCTG			intron-variant	NTNG2	GRCh38.p7	9:132167934	GTGACGTCTGTGGGC[-/TTCTG]TTCTGTCATCTGCAA	84628
rs772102274	snp	G/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240628	CCCTCTAGTTGCCCA[G/T]AGAGGGGAAGGGGCT	84628
rs772112693	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204770	GAGGAAACTGAGGCC[A/G]GGAGGTTGAGATATA	84628
rs772142777	snp	A/C/G	3.39866e-05	0.00412218	missense	NTNG2	GRCh38.p7	9:132197990	TACCTATGCAGCAAC[A/C/G]AGTGTGACGCCTCCA	84628
rs772157056	snp	C/T	1.65323e-05	0.00287505	intron-variant	NTNG2	GRCh38.p7	9:132197920	GCTTCCCAGGCCATC[C/T]CGAGCATCCAGCACC	84628
rs772200975	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132203844	CCCACGCAAGTTCCT[A/C]TGCCCAGAAAACCCA	84628
rs772348214	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211105	GCAGCCCGGGGTTCA[C/T]CAGAGGCCTTGGCTT	84628
rs772355340	snp	A/C	3.47681e-05	0.00416927	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240903	GCCCGTGCCCGTGTC[A/C]GTCCAGAGTGTAACT	84628
rs772409596	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132206603	ACCCAGAAGGCGGAG[C/G]TTGCAGTGAGCCGAG	84628
rs772425332	snp	C/G/T			intron-variant	NTNG2	GRCh38.p7	9:132176844	TTCTCCGAATCCTTG[C/G/T]CAACACTTGTTATTT	84628
rs772456975	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132177814	AGGCACTAGCCAGCA[C/T]GCCCAGCTAATTTTT	84628
rs772468558	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132180248	AGAAGTCTGCTGTCG[A/G]GCAAAAGGTGAAGAA	84628
rs772481366	snp	A/G	2.19715e-05	0.0033144	intron-variant	NTNG2	GRCh38.p7	9:132227046	ATGCCCCGGGGCCAC[A/G]AGCCCACATGGCTAT	84628
rs772486918	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132235723	CCGTGCAGAAGGTAT[-/G]GGGGGGGCAAGGCCT	84628
rs772544133	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223892	TAAAATCCCGCCTCC[A/G]TCTCCTGGTCTGGCC	84628
rs772548666	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132228246	GTGCAGAGGCCATGA[A/C]AGGCATGTCACGCGT	84628
rs772589066	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132197879	CAGGTTTCTCGGTTC[A/G]CAGGCAGGGGCTAGG	84628
rs772657615	in-del	-/GA			intron-variant	NTNG2	GRCh38.p7	9:132170713	CTGACGAGCAGGTGA[-/GA]GAGAGAGAGAGAACT	84628
rs772684331	snp	C/T	1.67947e-05	0.00289777	intron-variant	NTNG2	GRCh38.p7	9:132239301	ACACGGCACAGGGAA[C/T]TTGCTGGAATGCGTG	84628
rs772689013	snp	A/G/T	0.000116181	0.00762089	missense	NTNG2	GRCh38.p7	9:132198143	TCGTGGAACAAGACC[A/G/T]TGGAGCTGACCGACG	84628
rs772690864	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132238088	GGTGTTTCAAGAGGG[-/T]GGCCGTTGTCCTTCC	84628
rs772709823	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132175479	ATGGCCCCTGACCGG[A/G]GCTGACCTGGCCAGA	84628
rs772775556	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229349	CAAGTCTGGGGGTCA[C/G]CTTGACTGGAGACCC	84628
rs772776915	snp	A/G	0.00128123	0.0252779	intron-variant, missense	NTNG2	GRCh38.p7	9:132231521	GTGAGCCGAGAGGGC[A/G]CCAGAAAGAAGCTGG	84628
rs772778998	in-del	-/GCCCGCGGAT			intron-variant	NTNG2	GRCh38.p7	9:132186747	CCAAAGCGGAGCGAA[-/GCCCGCGGAT]GCCCACCGCCTCTCC	84628
rs772785647	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194002	GCCACCAGTCAGATT[A/G]GACTAGGGCCAACCT	84628
rs772792892	snp	C/T	4.78595e-05	0.00489157	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230642	CCCCCACTGCACGAG[C/T]CTCTTTGCATGTCCT	84628
rs772807460	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186926	CTCCCAGAGTTCACA[C/T]TCACAGAAGGTTCTG	84628
rs772815584	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132172164	GAATGCCTGCCCCCT[C/G]CTTCCTTTCTTTTCA	84628
rs772822182	snp	A/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240806	GTGGGGAGCATCCCC[A/T]GGGGAGTGTGGAGAT	84628
rs772897411	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132185719	CTCCTTTCATTTACT[C/T]TTTAAAAAAGTATGA	84628
rs772918307	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132224921	TATGTGTATCTCTCT[A/C]TGCTTTTTTTTTTCC	84628
rs772936212	snp	A/C	6.30955e-05	0.00561638	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241057	ACCGTGAGTGCGCGC[A/C]GTCCCCCGTGGGCGG	84628
rs772951473	snp	C/T			intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231549	TGGACCCTGCAGGGA[C/T]GCTGGTCTGCACAGC	84628
rs773021516	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196481	ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCTGGGT	84628
rs773028629	snp	A/G	1.71319e-05	0.00292672	intron-variant	NTNG2	GRCh38.p7	9:132241868	CTGACCGCCCCCTCC[A/G]CCTGCAGCCAACGTG	84628
rs773050590	snp	C/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230384	AGTGAGGATGAAATG[C/G]GATAATCCACCCCCG	84628
rs773075260	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132184749	ACCAACATGGGGAAA[A/C]CCAGTCTCTACTAAA	84628
rs773093351	snp	G/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159690	AGGCATGTTAAAAAT[G/T]GTTTCTAGTGGCACA	84628
rs773096701	snp	A/G	0.000121506	0.00779346	missense	NTNG2	GRCh38.p7	9:132198291	TCGGTATGTCCGCCC[A/G]CCGGGCCCGCGACAT	84628
rs773114211	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132213484	ATGTAAGCCCGCAGC[C/T]CCCTCCCAGGGCAGC	84628
rs773122403	snp	A/C			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239612	CTCAGTGGCAGAGGC[A/C]ACTGAGCATCTGTCT	84628
rs773134427	snp	C/T	6.7297e-05	0.00580034	intron-variant	NTNG2	GRCh38.p7	9:132239306	GCACAGGGAACTTGC[C/T]GGAATGCGTGCAGGG	84628
rs773179262	in-del	-/GT			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162570	TGAGAGAGAGACAGA[-/GT]GTGTGTGTGTGTGTG	84628
rs773213684	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194001	GGCCACCAGTCAGAT[C/T]GGACTAGGGCCAACC	84628
rs773241567	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200505	AAGTGTGTACAGGAC[C/T]GGGAAAAACATCATG	84628
rs773244121	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132233333	TGCACACGCACATGT[-/AC]ACACACACACACACA	84628
rs773280823	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132236838	AAGGCAGGTGCCGTC[C/T]GTGTTCCTGGCTTGA	84628
rs773302121	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132192822	TGTTGGCCGCGGCTC[A/G]GGATTTATTTATTGT	84628
rs773304088	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204775	AACTGAGGCCAGGAG[A/G]TTGAGATATAGATGG	84628
rs773329114	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132161400	TTTTGGAAGAGGAAG[C/G]TGCAGCCCGGCTGCG	84628
rs773352201	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132170004	CCTAATGGCGGCCAG[A/T]TGCCCACTGCCCCCT	84628
rs773442524	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201656	GTGACTGCCATGTTG[C/T]CCAGTGGCTCCGCTG	84628
rs773482857	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203213	GGCATGGTGGTGTGC[A/G]CCTGTAGTCCTAGCT	84628
rs773533551	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207386	GCTCCTGGTGGGGCC[A/G]GCAGCCTCTGGCGTT	84628
rs773543893	snp	C/G	1.71164e-05	0.00292539	missense	NTNG2	GRCh38.p7	9:132198525	GCATGCGGCTGCTGC[C/G]CCCGGCGCTGGGCGG	84628
rs773577953	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132227377	CACAGGGAAACCCGA[A/G]AGGAGCTGCTCAGCA	84628
rs773630204	snp	G/T	0.00044764	0.0149539	splice-donor-variant	NTNG2	GRCh38.p7	9:132198611	GAGGTCATCGGCAGG[G/T]AAGGCCGGGGGAAGC	84628
rs773659824	snp	C/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132231419	GCTTCTGGGGTGCAC[C/T]GTCACCCTCCACCAG	84628
rs773686144	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132217918	CCAGTGGGCACCGCT[C/T]TGTGCCAGGGCTTTT	84628
rs773709731	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132196950	ACGGAACTCAGAAAG[G/T]CATTTTCCCTACATT	84628
rs773787094	snp	C/T	0.000141563	0.00841198	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230528	GGTGACACCCAGGCC[C/T]CTTCCCCTGGGGCAG	84628
rs773788814	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132217807	CTTTCCTGAGGTCAC[A/T]CAGTCGTTGGCAGAA	84628
rs773799708	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132206611	GGCGGAGGTTGCAGT[G/T]AGCCGAGATCGTGCC	84628
rs773804550	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132165871	ATTAATAAAAATAAC[C/T]CAGTTTTCTCGGGAG	84628
rs773813804	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177877	GGCCAGGCTGATCTC[A/G]AACTCCTGGACTCAA	84628
rs773845683	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191517	ACTCAGGGCTTTCAG[A/G]CGCCAGGGCCCAAAA	84628
rs773847253	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132195782	CACAGGTGTGCACCA[C/G]TATGCCCAGCTAATT	84628
rs773868588	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132193752	GTCTTAGTCAGCTCC[A/G]GCCACCATAACAAAG	84628
rs773877377	snp	A/G	0.000282143	0.011874	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132230637	CAGGGCCCCCACTGC[A/G]CGAGCCTCTTTGCAT	84628
rs773884736	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132218935	ACTCACAGCTTTACC[C/T]AGATGTGATTCACAC	84628
rs773898652	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132214386	GCTCCTGCCTGGCAC[A/G]GGCCAGGGCCCCTGT	84628
rs773964839	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132227993	ACCCTCACACAGCCC[C/T]GCAGGGTGGAGTCCT	84628
rs774005461	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132185457	TCCTCCCTCCGTGAT[A/G]AAATATTCATGGCGG	84628
rs774010581	snp	C/T			intron-variant, missense	NTNG2	GRCh38.p7	9:132235669	GGACCAGGCCATCTA[C/T]GGCTGCCCCTCTCTC	84628
rs774014170	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132196750	GGTGTCCGATGATTC[C/T]GTTCAATTGTAACAC	84628
rs774063592	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132238638	TGCATCTTGTCCAGC[A/G]TCCATCCATGCATTC	84628
rs774091373	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132191102	CACCTGCCTCCTGTG[A/G]GTTGCTGAGAGGGTG	84628
rs774179124	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132202554	TCTCCTTCCACACAT[A/G]GGGAAACTCAGGTGC	84628
rs774246584	snp	C/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244936	CAGCCCTGGCCGGAT[C/T]CACGAGGCTGGGGGC	84628
rs774260722	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212389	CTTTGTAATGGGTAA[C/T]AGGATTTATCAATAG	84628
rs774280465	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132203495	AGACAGTGGACCAAA[C/T]ATTCCAGATCTTCTG	84628
rs774292594	snp	C/T	3.34443e-05	0.00408913	missense	NTNG2	GRCh38.p7	9:132198024	CGGACCTGGCCCACC[C/T]GCCCAGGCTCATGTT	84628
rs774294276	snp	A/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132239468	TTAGTAACCTACCCT[A/T]GCGGTTCTCCGGTAA	84628
rs774377311	in-del	-/TCAG			intron-variant	NTNG2	GRCh38.p7	9:132211928	AATTCATTCATTCAT[-/TCAG]TCAGTCAGTCATTCA	84628
rs774391854	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132169748	CGTGCTGCCGTGGTA[A/C]GTGCGGACACATAGT	84628
rs774466809	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204291	CTCTATGTCCCTGGG[C/T]CTCCCCCAACCTGTT	84628
rs774475762	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132220293	CCCATTCTGTGGGTT[G/T]TCTTTTCACTTTCCT	84628
rs774478909	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180861	CTCTTCCTAGAACCA[C/T]GCATGTGCACACGTG	84628
rs774492482	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240751	GCCACCCTGGGAAGT[C/T]CCCACCTGCCGTCCA	84628
rs774518120	snp	A/C			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166031	CTTACAATGAAAGAC[A/C]AGTCAGACCCCAGGT	84628
rs774540999	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132199231	ACTGTGAGAAGTGCT[C/G]TGAGGCTGTCCACTG	84628
rs774582511	snp	C/T	3.51482e-05	0.004192	missense	NTNG2	GRCh38.p7	9:132226965	AGAAGAATTTCCGCA[C/T]CCGGTCCTGGCGGGC	84628
rs774584115	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132209401	GGGGAGTCCTGAGCT[C/T]CGCGGTGACGATGAC	84628
rs774621279	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132224653	AAAATAGGATTCTAC[C/T]AAACCCATTGCTCTG	84628
rs774627187	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132178150	GACTAGGCCACAGTG[A/G]GGCCTGAGGAGGGGA	84628
rs774648360	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226170	CCCTCATCAACTTTC[A/G]GTTACCCCGAGGTAC	84628
rs774678499	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132168086	GCCGTTGTCATTCTG[C/G]TCATACAGGTGGGGT	84628
rs774772834	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201566	AAGTTCCTGAGTGGG[C/T]ACCAGGGACCCCTGG	84628
rs774784247	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132205835	GCAGTGAACTGAGAT[C/T]GCACCACTGCACTCC	84628
rs774797812	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243906	ACCCGGAAGTGCCTT[C/T]CGACAGGCCCTGCAT	84628
rs774864300	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132180095	TGTCTTGGGTCTCTC[A/T]GGGACCGTTTGGGCC	84628
rs774875445	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132175941	GGACTCCAGTGCAGA[C/G]AGAGGGGTCCTAGAT	84628
rs774879562	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232348	GGAGCCTCTGGAGCT[A/G]AGTTTGGACACCGTG	84628
rs774922754	snp	G/T	1.69974e-05	0.0029152	synonymous-codon	NTNG2	GRCh38.p7	9:132198400	GCGCTTCGAGGTGCG[G/T]GACCGCTTCGCCATC	84628
rs774924316	snp	C/G	0.000171091	0.00924751	missense	NTNG2	GRCh38.p7	9:132241943	GCAGAACCAGCGCTG[C/G]GCCTGCCCGCGCGGC	84628
rs774953083	snp	A/G	1.70519e-05	0.00291987	missense	NTNG2	GRCh38.p7	9:132198383	AAGAAGGAGAAGCAC[A/G]TGCGCTTCGAGGTGC	84628
rs774953946	snp	C/G/T			intron-variant	NTNG2	GRCh38.p7	9:132205075	ATGGTGGCTCCTGAA[C/G/T]AAGTTACATGTAGAT	84628
rs774959809	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176834	GAATGCCAGTTTCTC[C/T]GAATCCTTGTCAACA	84628
rs775011799	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234057	TTTGAGATGGAGTTT[C/T]GCTCTTGTCGCTGAG	84628
rs775038363	snp	C/T	0.000183739	0.0095831	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132242049	CCCGGGGCCGCCCCG[C/T]GCCCCGCCACCCTGC	84628
rs775047519	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132176114	AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA	84628
rs775063814	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132234395	GCAGACCGGGCTTCC[A/T]TGGGGCCTTGGCACA	84628
rs775083330	in-del	-/TC			intron-variant	NTNG2	GRCh38.p7	9:132211566	ACCCCAAAGGCTGGG[-/TC]TCTCGGGCTGGCCTA	84628
rs775150248	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205782	CCTACTTGGGAAGCC[A/G]AGACAGGAGAATCAC	84628
rs775228614	snp	A/G			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244844	TCCTCCTAGTCATCA[A/G]GATGATAAAATGTCA	84628
rs775323369	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211423	CTAAACACAAACCCA[A/G]TCACTTCTCTGCACA	84628
rs775327814	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132183450	TTTGCTCAGTCGACC[A/T]AGAGCACCATCCTCC	84628
rs775339440	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132182275	ATTGCACCCAACAAT[A/G]GACAATAATGGGCCT	84628
rs775401695	snp	C/G	1.67626e-05	0.002895	missense	NTNG2	GRCh38.p7	9:132198013	CGCCTCCAACCCGGA[C/G]CTGGCCCACCCGCCC	84628
rs775421219	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132221862	TTGGATTCGGCCGGT[C/G]TTCTATGCATCTTTA	84628
rs775432202	snp	A/C	1.65002e-05	0.00287225	intron-variant	NTNG2	GRCh38.p7	9:132197933	TCCCGAGCATCCAGC[A/C]CCCACCCTTCCCTTC	84628
rs775465174	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132232452	GTCTGCCACAGACAG[C/G]CATGGAAACCTGATT	84628
rs775520045	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132171132	TTCTGAGCAGGAGCC[A/G]GTGGAAGGTTCCAGA	84628
rs775520883	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132238792	GCATCCTTCAGCGAG[C/T]GCTTGGCCCTGGTGC	84628
rs775521619	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132208112	CTATCTCAAAACCCA[A/G]GGCAATATGGGAGTG	84628
rs775524745	snp	C/G/T	3.30034e-05	0.00406212	synonymous-codon	NTNG2	GRCh38.p7	9:132166852	GCATCTGCTGGCGCT[C/G/T]TTCCTGCACTGCCTC	84628
rs775532751	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230255	TGCGTGTGAAGCTCC[C/T]AGTGGAGCGTTTGGC	84628
rs775595149	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132163984	AAAACGATCCTCCGG[C/G]ATGCAGCTTCTTACT	84628
rs775601844	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132223647	GGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACT	84628
rs775608030	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132170117	CGGGAGCGCAAGCCC[A/G]GCTGCACTCCGAGGG	84628
rs775608833	snp	A/G	1.83451e-05	0.00302857	missense	NTNG2	GRCh38.p7	9:132226868	AAGTGCAACCTGCAC[A/G]CCAACCTGTGCTCCA	84628
rs775609551	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132220156	GGAGAAATGTCTGTG[C/T]TGATCCTTTCCTCAT	84628
rs775628996	snp	A/G	1.81066e-05	0.00300882	intron-variant	NTNG2	GRCh38.p7	9:132198625	GTAAGGCCGGGGGAA[A/G]CCCTGGATGTCACCT	84628
rs775639330	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167392	GTCAGCATTCTGGGC[A/G]AGTGAGCAAGATGCT	84628
rs775640763	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184543	GCCAAAGGCTGGAGG[A/G]AGAGCTGTAGACAGA	84628
rs775721503	snp	A/G	5.67408e-05	0.00532609	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241047	CAGGGCTGCTACCGT[A/G]AGTGCGCGCCGTCCC	84628
rs775785502	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132234996	TTTGGGCACAGGGCA[A/G]TTCTTTGCCAGCCCT	84628
rs775820559	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132165857	TGTGCAACTCTGATA[A/T]TAATAAAAATAACCC	84628
rs775847891	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132167989	ACACTCCTAGGGTCA[C/T]TGTGAGGAGTTTGTG	84628
rs775875620	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132186750	AAGCGGAGCGAAGCC[C/T]GCGGATGCCCACCGC	84628
rs775883068	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132197107	GGTAAAAAGGCTCAG[G/T]GGCCGGGCGCAGTGG	84628
rs775933387	snp	A/G	1.64876e-05	0.00287116	missense	NTNG2	GRCh38.p7	9:132166956	ACGCCTGCCAGCCCA[A/G]GGTGATGCGCCTGAA	84628
rs775981811	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132213544	ACCCCAGCTCTGTGA[A/G]TCCTCAGAAAGCGAG	84628
rs775994232	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132199058	CCTGATATTACATCA[C/T]AGGGACTGCCTAGGA	84628
rs776022244	in-del	-/C			intron-variant	NTNG2	GRCh38.p7	9:132185608	CTTTCCTGGGCTTCT[-/C]CGGATGTAGCCCTCT	84628
rs776051799	snp	A/T	1.69086e-05	0.00290758	intron-variant	NTNG2	GRCh38.p7	9:132239048	TCCTCGCCCTGTCCC[A/T]CAGTTTCCCTGAATG	84628
rs776102358	snp	C/T	1.71714e-05	0.00293008	intron-variant	NTNG2	GRCh38.p7	9:132239037	GGGTGAGTCCTTCCT[C/T]GCCCTGTCCCTCAGT	84628
rs776111951	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132176179	TGTAGTGAGACCCCA[A/T]CTCTCAAAAAAAAAA	84628
rs776146430	in-del	-/CCATCCCA	3.20862e-05	0.00400526	intron-variant	NTNG2	GRCh38.p7	9:132197922	TCCCAGGCCATCCCG[-/CCATCCCA]AGCATCCAGCACCCA	84628
rs776175811	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204297	GTCCCTGGGCCTCCC[C/T]CAACCTGTTTTTTCC	84628
rs776190927	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132200145	GCCTGGCACATAATA[C/T]GCACTAAAAAAAAGT	84628
rs776214481	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132159908	GCCCTGGGGTGACAG[C/T]AGGCTGAGGGCTGAC	84628
rs776216938	in-del	-/TAA			intron-variant	NTNG2	GRCh38.p7	9:132193122	TGGGCAGGGCAGGGC[-/TAA]TAAGTAAGGCAGGAA	84628
rs776220975	snp	A/G	1.66468e-05	0.00288498	synonymous-codon	NTNG2	GRCh38.p7	9:132198166	GACCGACGACGTGGT[A/G]ATGACCTTCGAGTAC	84628
rs776223912	in-del	-/CTG			intron-variant	NTNG2	GRCh38.p7	9:132175852	TTCATTCAATGTTCC[-/CTG]CTGATTGCCAGGTAC	84628
rs776272173	snp	C/T	1.64925e-05	0.00287158	synonymous-codon	NTNG2	GRCh38.p7	9:132166981	CCTGAAGGACTACGT[C/T]AAGGTGAAGGTGGAG	84628
rs776285824	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132204955	TGAGGATGGCTATTA[C/T]TGGAAAAGCAAAAAA	84628
rs776375171	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132214793	GAATCGTTGTTTTTT[A/G]GGGTAAGTATGTCCC	84628
rs776404883	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132241685	GCGGTGGGAGGCAGC[C/T]GGGGGCCAGATCTCG	84628
rs776411686	snp	A/G			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160428	GGCGAAGATTCAGTG[A/G]ATAATGCACACAAAC	84628
rs776457277	snp	C/T			utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166454	GCAATCTGATCCAGC[C/T]TCATGCAGGATCCCT	84628
rs776554771	snp	A/G/T	0.00017943	0.0094701	intron-variant	NTNG2	GRCh38.p7	9:132198618	TCGGCAGGTAAGGCC[A/G/T]GGGGAAGCCCTGGAT	84628
rs776559564	snp	A/G			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230445	TAGCAGTTGTGTGGT[A/G]GAGCAGGTGCTCTTG	84628
rs776560043	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132194108	GGTTAGGGCTTCAAC[A/G]TAGAAATCTGGGGGA	84628
rs776600702	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132168125	CAGCCCAGGGGTGAC[A/G]GGTAAAGGCATCTGG	84628
rs776635613	snp	C/T	1.79735e-05	0.00299774	missense	NTNG2	GRCh38.p7	9:132226976	CGCACCCGGTCCTGG[C/T]GGGCCGGCTCCTACC	84628
rs776636166	snp	A/G			missense	NTNG2	GRCh38.p7	9:132239230	GGCTGGGCTACTACC[A/G]CAACGGCTCGGCAGA	84628
rs776639607	snp	C/T			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132243681	GTTCTTTCCCAGCTG[C/T]GAGGTTTAGACCTGG	84628
rs776654042	snp	A/C	0.000202645	0.0100639	missense, synonymous-codon	NTNG2	GRCh38.p7	9:132241920	TGCCAGAACGGAGGC[A/C]CCTGCCTGCAGAACC	84628
rs776687231	in-del	-/AAGA			intron-variant	NTNG2	GRCh38.p7	9:132187569	AGAGCGAGAGGGAGC[-/AAGA]GAGAGAGAGAGAGAG	84628
rs776690233	in-del	-/AAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132190242	CCATCTCAAAAAAAA[-/AAAAAAAAAAA]AAAAAAAAAAGAAGG	84628
rs776738611	in-del	-/AA			intron-variant	NTNG2	GRCh38.p7	9:132219575	AGACTCTGTCTCAAA[-/AA]AAAAAAAAAAAAAGA	84628
rs776741370	snp	C/T	3.89385e-05	0.00441223	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241070	GCCGTCCCCCGTGGG[C/T]GGGGCCTGCGGAAAG	84628
rs776749355	snp	G/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132229499	CACCTGGCCAGCCCA[G/T]CACCCTCCAGGGCCC	84628
rs776762036	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132195308	CTTTTTTTTGTTTTC[A/G]TTTTTGTTTTTGTTT	84628
rs776762925	snp	C/T	1.7498e-05	0.00295782	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240937	ACCAGATAGGCTCCG[C/T]GCACGACCGGTGCAA	84628
rs776791401	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132177992	CATCAAGCATTCTAT[G/T]TGCACTACTTCATGA	84628
rs776810759	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132203424	CCTATGGTACCAGCG[G/T]AAGCGATAGGGAAGG	84628
rs776868360	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132166279	GAGAACCCAAGTCCA[A/G]TCCCAAAGAGGGAAC	84628
rs776907959	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132184091	CTACTCGCACCCACC[C/T]CCAACGACGAGCCAG	84628
rs776979719	in-del	-/TTT			intron-variant	NTNG2	GRCh38.p7	9:132234027	TGAGGTAGAGCTATC[-/TTT]TTTTTTTTTTTTTTT	84628
rs776992190	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179659	AATTCAGAGAAAGAC[A/G]CTGTGCAAAGCACCC	84628
rs776995559	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132217990	GTGGTCCATATCGCT[C/T]CTCAGGGCCAGTGTC	84628
rs776995773	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132163252	GGCTCGCAGCCGGCC[C/G]GAAGCACTGACTCGA	84628
rs776996519	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132238570	GTCTGGCAGGTGGGC[A/G]TTTTCCTCCCAGCCA	84628
rs777018446	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132217057	TGTGAGATCCAGCTC[C/T]AGTGCCATGCAGCCC	84628
rs777056403	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219126	GGAGGCTGAGGCAGG[A/G]GAATCACTTGAACCC	84628
rs777103560	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207493	GCTGTCTCCCCGTGT[C/T]TCTTCCTACAGGGAC	84628
rs777145908	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234827	ATTAAAGTCAATTCA[C/T]GTCCAAAGCTCCCCG	84628
rs777191929	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132218980	ACATGTAAAGCGTAC[A/T]ATTCAGTCGCTTTTA	84628
rs777214155	snp	A/G/T			intron-variant	NTNG2	GRCh38.p7	9:132198925	TCTGGTACCTGGGAC[A/G/T]TGACCTGGTTCTTGG	84628
rs777220774	snp	A/G			missense	NTNG2	GRCh38.p7	9:132198191	GAGTACGGCCGGCCC[A/G]CGGTCATGGTCCTGG	84628
rs777245247	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132194448	TTCCAGGCAACAGCA[C/G]AGGACAGGGTGTGTC	84628
rs777317822	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132221907	ATGTTATCACCCAAA[A/G]TTGATGGCAATCTTT	84628
rs777331301	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207879	GAGGCTGAGGCTGGC[A/G]GATTGCTTGAGCGCA	84628
rs777338213	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208856	GGCCCACAACAGCCC[A/G]TCTCTCCAAGAACTC	84628
rs777355691	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132218735	CTCCTGACCTCAGGT[G/T]ATACACCCGCCTCGG	84628
rs777396453	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132214503	AGGTGAGGCCCGGTG[C/T]TGCCTACTAACAGTT	84628
rs777423421	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167113	GAGGAGATCCTTGGG[A/G]TGGACGAGCAGAGCT	84628
rs777449367	snp	A/G	1.64874e-05	0.00287113	missense	NTNG2	GRCh38.p7	9:132166913	AAATCCTGGGTGACC[A/G]CAGATGAGGGCCCCA	84628
rs777524445	snp	A/G	5.26764e-05	0.00513181	synonymous-codon	NTNG2	GRCh38.p7	9:132226915	GCAGTGCGAGTGCGA[A/G]CACAACACCACCGGC	84628
rs777543822	snp	A/G	1.69591e-05	0.00291191	synonymous-codon	NTNG2	GRCh38.p7	9:132198463	CCTCTACACGCGGCT[A/G]GAGAGCGCCAAGGGC	84628
rs777591838	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132226642	AGTGACTGCAGGTGT[A/G]GCCTTTGGAACACGG	84628
rs777622980	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132167918	GGAGGGCTCTGGCCC[A/G]GTGACGTCTGTGGGC	84628
rs777649820	snp	C/T	1.65666e-05	0.00287802	intron-variant	NTNG2	GRCh38.p7	9:132239101	CCCACTTGGCCGGCC[C/T]AGACTGCGAATGCTA	84628
rs777683160	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132223580	CAATCTCTGAATGGA[C/T]GAGAGCCAGTCAGGG	84628
rs777686749	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132234934	AATCCCTTCAAGAAG[C/T]GGAAAACAGCAGCGC	84628
rs777758403	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132188787	CTGTGAAGCCAGTGC[A/T]AGTAACCTCATTGAG	84628
rs777770779	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132192801	AAAGAGGGAGAGAGA[A/C]AATTGTGTTGGCCGC	84628
rs777834607	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174748	CCAACATGGGGAAAC[C/T]CCGTCTCTACTAAAA	84628
rs777902000	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132202132	GCCTGTATGATGGAG[C/T]GATCCCACGGGACTC	84628
rs777906124	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132212990	ACGTCTTGACTCAGG[C/T]CTGGGCATAGCAGAT	84628
rs777908381	in-del	-/AC			intron-variant	NTNG2	GRCh38.p7	9:132175928	CACACAAAACAGTGG[-/AC]TCCAGTGCAGACAGA	84628
rs777945349	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132205394	TTCTGCTTACCCGAC[A/G]TCCCCAGAGTCGTCA	84628
rs777990612	snp	C/T	1.64866e-05	0.00287106	intron-variant	NTNG2	GRCh38.p7	9:132226835	ACATCTCTGCCCTCT[C/T]GGTGTCTCCCCAGGT	84628
rs778008607	snp	C/G	2.2002e-05	0.0033167	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241015	GCGACGACTGCCTCC[C/G]CACGCACTACTGGCG	84628
rs778016269	snp	C/G	0.000163199	0.00903176	intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231337	CGCCATCTGCTCTGC[C/G]AGGCAGCAGGAGAGG	84628
rs778089138	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179542	GATCGCAGCAATGCC[A/G]GCGATCATGGTGCTG	84628
rs778100842	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132203188	GGAAACACAACTTAC[A/G]TGGAAGCCAGGCATG	84628
rs778106155	snp	C/T	4.60384e-05	0.00479761	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230578	CTCCCACAGGTGCCA[C/T]TGCAGGTTCCTTTGG	84628
rs778206291	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132184535	AGACACCTGCCAAAG[A/G]CTGGAGGGAGAGCTG	84628
rs778206895	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132193411	AGATTGATTCAAGTC[A/C]GGAGGGCCTCCTGGA	84628
rs778231556	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162792	CAGAGAAACTCCCGG[C/T]CAGTCCGGCTGGAAA	84628
rs778295843	snp	C/T	3.47307e-05	0.00416703	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240906	CGTGCCCGTGTCCGT[C/T]CAGAGTGTAACTGCA	84628
rs778310992	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132173323	CCCTCCTGGGCAGTA[C/G]ACAATGAGAAGACCG	84628
rs778358832	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132207799	GTGCCCACAGGTGCA[C/T]GGTGAGAAAGAAACC	84628
rs778366149	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132219808	ATTAGCAATGCTGCT[A/G]TCAACATTCATGTAC	84628
rs778436661	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132162300	TGCAGCTTGGCCAGG[A/C]CGGTTTCATTTTTAA	84628
rs778448978	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132219705	TCAGTATTTCATTAC[C/T]TTTTCTGGCTGTATA	84628
rs778451271	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218824	GTTTATAAAAATAGG[A/G]AAACAAATCTCTGAA	84628
rs778456367	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183387	TCAGCAGCGTGCATG[C/T]GTTAACCCATTGCCC	84628
rs778494455	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132191484	TCACAGAGCCTCAAA[G/T]GAGAGAGCTGAGAGG	84628
rs778551738	in-del	-/A			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230229	CCAAAAATCTGAAAT[-/A]AGAGGAGGAGTGCGT	84628
rs778560951	snp	C/T	1.66924e-05	0.00288893	intron-variant	NTNG2	GRCh38.p7	9:132239075	AATGCTCGCTGACCA[C/T]TGGTATTTCTCCCAC	84628
rs778580807	snp	C/T	3.66737e-05	0.004282	intron-variant	NTNG2	GRCh38.p7	9:132226832	CTGACATCTCTGCCC[C/T]CTCGGTGTCTCCCCA	84628
rs778588337	snp	C/G	0.000137667	0.00829544	missense, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240988	GCCGCGAGGGCGCGG[C/G]GGGCCCCAAGTGCGA	84628
rs778618276	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132234543	GAGTGCCTCCCAACA[G/T]GTGCTTCGGGCTCTT	84628
rs778647368	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132207161	GAGCTTTCTCGCCAT[A/C]ATATTAATTCACTCA	84628
rs778667286	snp	A/C	0.000106763	0.0073055	intron-variant, synonymous-codon	NTNG2	GRCh38.p7	9:132231450	GGCTCTGTGGGGCCC[A/C]ACATCCCACCCAAGT	84628
rs778670533	snp	C/T	1.6498e-05	0.00287206	synonymous-codon	NTNG2	GRCh38.p7	9:132198595	CGCCATCTCCAACAT[C/T]GAGGTCATCGGCAGG	84628
rs778689084	snp	C/T			missense	NTNG2	GRCh38.p7	9:132166848	TGCTGCATCTGCTGG[C/T]GCTCTTCCTGCACTG	84628
rs778696119	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132176777	CACCAAACTGTTTTC[A/T]ACAGGTGCTGCACCT	84628
rs778705406	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132218420	TCATGCAAAGTGAGC[A/G]CTCACGCATCAGCTG	84628
rs778715042	snp	A/G					GRCh38.p7	9:132195817	AATTTTTTTTTGTAG[A/G]TACAGGGTCTTGCTG	84628
rs778753703	snp	C/T	1.8126e-05	0.00301042			GRCh38.p7	9:132198285	AGGCCTTCGGTATGT[C/T]CGCCCGCCGGGCCCG	84628
rs778758230	in-del	-/TA					GRCh38.p7	9:132239507	TGGAGTTGCAAAACT[-/TA]TACCAGTGGCCCTTC	84628
rs778772173	snp	A/C	2.25502e-05	0.00335777	intron-variant	NTNG2	GRCh38.p7	9:132239001	TTCCAAAGATGCCTT[A/C]CTCCGTCCCTGCATG	84628
rs778804351	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188642	CATGCTCCCTAACGG[C/T]GGGGCCTGCTGTTTG	84628
rs778823686	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132224646	TTTAATAAAAATAGG[A/G]TTCTACTAAACCCAT	84628
rs778849152	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132232117	GAACTGAGAGGAAAG[A/G]TGCTGGGGGCAGCGA	84628
rs778849176	snp	A/C	1.65332e-05	0.00287512	intron-variant	NTNG2	GRCh38.p7	9:132197915	CAGAGGCTTCCCAGG[A/C]CATCCCGAGCATCCA	84628
rs778853678	in-del	-/GCCCGT	1.7487e-05	0.00295689	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240887	TAGCCCTGACCGCGC[-/GCCCGT]GCCCGTGCCCGTGTC	84628
rs778862200	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132173506	ACCTTTCCGGTCTGC[A/G]CATCCCCACCTTCCC	84628
rs778865723	snp	A/G	8.50847e-05	0.00652189	intron-variant	NTNG2	GRCh38.p7	9:132227038	TACGTGCCATGCCCC[A/G]GGGCCACGAGCCCAC	84628
rs778934905	in-del	-/TTGTC			intron-variant	NTNG2	GRCh38.p7	9:132225224	GCTGGCCCTTTTGTT[-/TTGTC]TTGTCTTGTTTTGTT	84628
rs778997168	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132212939	TCTCCCAACCCCCCA[A/G]AGAAGACCAAGATCC	84628
rs779037806	snp	C/T	2.63758e-05	0.00363142	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132230565	CACGCCCGTCTCTCT[C/T]CCACAGGTGCCACTG	84628
rs779046890	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132211058	CCCCTGCTCACAGAC[A/G]CGGACCCACAGGGTG	84628
rs779120272	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132194938	TGGGCCCCATTTCCC[A/C]CATGGGGGCCAAACA	84628
rs779151358	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132183220	CCACTTAAGCCCTCA[C/T]ACTTTGTTCCCAGGC	84628
rs779155780	in-del	-/TC			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160711	GTGACCTTGGGCTGG[-/TC]TCTCTCTCTCTGCCT	84628
rs779202665	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233016	CAGGAGGCATTTACA[A/G]GAGGCAGGGGCTAGC	84628
rs779228552	snp	C/T	4.26667e-05	0.00461861	synonymous-codon, missense	NTNG2	GRCh38.p7	9:132242000	CCGCTGCGACCCCGC[C/T]GACGATGACGGCGGT	84628
rs779244063	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132211895	CCAGAACCAGGTAGG[C/T]GTGCTGTATATGTGT	84628
rs779246289	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132190443	GATTTCATCCCAGCG[C/T]AGGCTTGGGTGCAAG	84628
rs779248661	in-del	-/TG			intron-variant	NTNG2	GRCh38.p7	9:132208058	GCAGTGAGTTATGAC[-/TG]TGCTACTGCACTCCA	84628
rs779257008	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132169929	TGGAAGATGCAGGCT[-/G]GGGGGAGCTTCCTCG	84628
rs779344403	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132171682	TGGGCTGTTGAATGC[A/C]GACAGCAGGCAGGTC	84628
rs779432369	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132203107	ACCCACCCCAGGTAC[G/T]AGAAGGAGTGTGGAA	84628
rs779462641	in-del	-/CT			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165997	TGTTGCTAATGAGCT[-/CT]CTCTCTCTCTCCTCC	84628
rs779487131	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132171661	TTCCTCCCCCAGGGG[G/T]TCTGCTGGGCTGTTG	84628
rs779518261	snp	C/G	1.72755e-05	0.00293895	missense	NTNG2	GRCh38.p7	9:132197978	CAGGAGAATCCCTAC[C/G]TATGCAGCAACGAGT	84628
rs779557014	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132179865	GAATGGTCGTTCTGA[A/C]ATTGAGAGCTAGCGG	84628
rs779597491	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132238848	CCACTGGCCCTCCCT[C/G]GTTCCCTGCCCACAG	84628
rs779599436	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132228094	TGAGTTGCATGCCAA[C/T]GCCAGGGCTTAGGGC	84628
rs779610581	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132235261	CACATGTCCCACTTC[A/G]CAGCCATTAGCCAGA	84628
rs779615471	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132206389	ACCCAACTCTTGGCC[A/G]GGCGTGGTGGCTCAC	84628
rs779696071	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132201884	CCTGGAGCGCTCCCC[A/G]CGGGGGCAGCGCTCC	84628
rs779714420	snp	A/G	5.2573e-05	0.00512677	intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240875	CGGCGCCCACACGTA[A/G]CCCTGACCGCGCGCC	84628
rs779741619	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132236929	AGTGTTTCAGAAAGG[A/C]AGGGAGATGCCAAAG	84628
rs779770817	snp	C/G			utr-variant-3-prime	NTNG2	GRCh38.p7	9:132244481	CACCGCACCACCTGC[C/G]TGTCTTACTGTGTGA	84628
rs779796903	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132176579	CACCATATTTTGTGT[A/G]TCCGTTTCCTAACTG	84628
rs779800577	snp	C/T	1.67393e-05	0.00289299	intron-variant	NTNG2	GRCh38.p7	9:132239283	ATTGGTGAGAGGGCA[C/T]GGACACGGCACAGGG	84628
rs779813862	snp	A/G			missense	NTNG2	GRCh38.p7	9:132198555	GCACCTATGTGCAGC[A/G]GGAGAACCTCTACAA	84628
rs779831418	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216107	CAGAGGTTTGAACCC[A/G]ACTGTCTGGCCACCG	84628
rs779919289	snp	G/T	4.97814e-05	0.00498881	utr-variant-5-prime	NTNG2	GRCh38.p7	9:132166806	CCAGGGCTTCTCTGG[G/T]CCGCGCCTCTGCAGA	84628
rs779929170	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132218641	AGCTGGGATTACAGG[C/T]GCATGCCACCACACC	84628
rs779930174	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132207068	TTGGGAGAGAGTCAC[A/G]CACAGCAACGCCTTC	84628
rs779932643	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132172398	TGATCTCTGATGTGA[C/G]ACCTAACCTCTCTGA	84628
rs779932683	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132195462	TACAGGCGCCCACCA[A/C]CACGCCTGGCTATTT	84628
rs779953135	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237594	CCGCTGGAAAAAGAC[A/G]GTGCAGGATAGAGGA	84628
rs779980242	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132233213	GTGGTGGTGGGTGCT[A/G]TGCCTGTCTCCAAAC	84628
rs779981225	in-del	-/CC			intron-variant	NTNG2	GRCh38.p7	9:132186682	GTTCTGTGGGGGCAA[-/CC]CGAATTGGTGTAAGA	84628
rs779985631	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132193390	TGATGAGAGAACTGG[G/T]TTCAAAGATTGATTC	84628
rs779991451	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132204611	TGACTCCTTGAAACT[C/G]TGGGAAGGCAGAGAC	84628
rs780062981	snp	C/T	9.43708e-05	0.00686851	intron-variant	NTNG2	GRCh38.p7	9:132241849	GACCGGGCCACCCCC[C/T]GTGCTGACCGCCCCC	84628
rs780080004	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132197472	AGAGAGTCGAGAATG[G/T]GAATGGGAATTTTTG	84628
rs780083113	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132224538	CACCATCAGGTCAGG[C/G]AGCCATCTGCTTTGT	84628
rs780085300	snp	A/G	1.73902e-05	0.0029487	synonymous-codon	NTNG2	GRCh38.p7	9:132226951	CTGCGGCAAGTGCAA[A/G]AAGAATTTCCGCACC	84628
rs780144669	snp	C/T			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132240540	CAGCAGCCCCAGACA[C/T]GCTCAGTGGCCTCTG	84628
rs780157790	snp	A/C	0.000446828	0.0149404	missense	NTNG2	GRCh38.p7	9:132241983	GTGCGCTGCGAGCAG[A/C]CCCGCTGCGACCCCG	84628
rs780180768	snp	C/T	1.71888e-05	0.00293157	synonymous-codon	NTNG2	GRCh38.p7	9:132198349	CTGCACCGAGGAGTA[C/T]TCGCGCTGGGCAGGC	84628
rs780188500	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132193833	CTGGAGGCTGAAAGT[C/T]CAAGATGAAGTTGTT	84628
rs780256272	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231208	CCAGGAGGGCGAGGG[C/T]GACATGGCGCCCACA	84628
rs780272934	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132215841	CCTGGGAGCCCATGT[A/T]CTCTCATCTCCGTCC	84628
rs780281572	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132222324	GGGCCGCCCGTACCA[A/G]TAGGTGCCTGCTGTC	84628
rs780294490	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132161065	CCTGCCCCACTACTC[C/T]GCACTCCCTGCAGAG	84628
rs780347618	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132209506	GACAGGGGGAATCTG[G/T]CAGGGCGGTGCCCCA	84628
rs780375469	in-del	-/TATTTCTCC	1.66838e-05	0.00288818	cds-indel	NTNG2	GRCh38.p7	9:132239266	TGATGAGAACGTCTG[-/TATTTCTCC]CATTGGTGAGAGGGC	84628
rs780395547	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188412	CCCTTTTGGGTGAAG[A/G]GCACCATTTCCCAAT	84628
rs780407387	snp	C/T	3.36922e-05	0.00410426	synonymous-codon	NTNG2	GRCh38.p7	9:132167044	GAGGTTCTGCTCCCA[C/T]GTAAGTCCACTTACT	84628
rs780497295	snp	C/G/T	0.000104258	0.00721937	intron-variant	NTNG2	GRCh38.p7	9:132227036	TGTACGTGCCATGCC[C/G/T]CGGGGCCACGAGCCC	84628
rs780534126	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132226784	GGAGGCGCTCCTTTC[C/T]CCAGAGGCCAGGCCA	84628
rs780541556	snp	A/G	1.67139e-05	0.00289079	intron-variant	NTNG2	GRCh38.p7	9:132239278	TCTGCATTGGTGAGA[A/G]GGCACGGACACGGCA	84628
rs780587259	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132224452	AAATCCCTGTGTGCC[A/T]CCTATTTATCCTCCC	84628
rs780603135	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132201014	GGCCCTGCAGGCTCC[C/T]GGCTTGTCTTCTGAC	84628
rs780669290	snp	A/G	1.70717e-05	0.00292157	synonymous-codon	NTNG2	GRCh38.p7	9:132198376	AGGCTCCAAGAAGGA[A/G]AAGCACGTGCGCTTC	84628
rs780741930	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132236274	AGCCTGACAAAGTGG[A/G]AAATGTGTGGGTTAA	84628
rs780762478	snp	C/T	4.96208e-05	0.00498076	synonymous-codon	NTNG2	GRCh38.p7	9:132239117	AGACTGCGAATGCTA[C/T]GGTCACTCCAACCGC	84628
rs780839401	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132199911	CATAGGAGATGAAAG[C/T]AGCCTTTACCTCCCA	84628
rs780865062	in-del	-/ACC			intron-variant, utr-variant-3-prime	NTNG2	GRCh38.p7	9:132208823	GGATAGAGTCATGCA[-/ACC]ACCACCACCACAGCC	84628
rs780907609	in-del	-/GTGTGTGT			intron-variant, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132162537	CGTGTGTGTGAGAGT[-/GTGTGTGT]GTGTGTGTGTGTGTG	84628
rs780938253	snp	A/G	1.66255e-05	0.00288314	missense	NTNG2	GRCh38.p7	9:132167031	GAGACCCCCCTGAGA[A/G]GTTCTGCTCCCATGT	84628
rs780959655	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132179325	CCAGCCTGCTTAGGT[A/G]AGCTCCCGCCTATGT	84628
rs781037813	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132236625	CTGAGGCTCGGTTCC[C/T]AGAAACCTGGAGGAC	84628
rs781065546	snp	C/G	1.6955e-05	0.00291157	synonymous-codon	NTNG2	GRCh38.p7	9:132198481	GAGCGCCAAGGGCCT[C/G]AAGGAGTTCTTCACC	84628
rs781076390	snp	G/T			downstream-variant-500B	NTNG2	GRCh38.p7	9:132244722	CGAGGAGTCCACCTC[G/T]GTCCAGAACAGGACT	84628
rs781128081	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132213129	AGCCTGGCCAACATA[C/G]TAAAACCCTCGTCTC	84628
rs781146788	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132196540	ATGCATCCACCACTG[A/C]AGTATTATACGGCAT	84628
rs781187380	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132180848	AGAATCCATGGTGCT[C/T]TTCCTAGAACCACGC	84628
rs781222829	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132232213	CTGGAGCCCCGCCCA[C/T]ACCCTGTCCCCACCT	84628
rs781229877	snp	A/C	5.13149e-05	0.00506506	synonymous-codon, upstream-variant-2KB	NTNG2	GRCh38.p7	9:132241037	CTACTGGCGCCAGGG[A/C]TGCTACCGTGAGTGC	84628
rs781247690	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132177366	CATATCTAAGAAACC[A/G]CTGCTAAATCCAAGG	84628
rs781419937	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132225753	GACCAGAGGAGCTTC[A/C]CTTCTGCCATTAATT	84628
rs781430143	snp	C/G	1.71678e-05	0.00292978	synonymous-codon	NTNG2	GRCh38.p7	9:132198256	CTACCAGTTCTACGC[C/G]GAGGACTGCATGGAG	84628
rs781436548	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132204460	GGTGGGCAGGTGGGC[A/G]CGGGGAGGGGAGTGC	84628
rs781518922	snp	C/T	3.97338e-05	0.00445705	intron-variant	NTNG2	GRCh38.p7	9:132227025	CTCCCAACGCCTGTA[C/T]GTGCCATGCCCCGGG	84628
rs781530462	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132213909	ACCAGGCAATGTGAT[G/T]AATGACCAGGAACCC	84628
rs781539105	snp	A/G	1.7487e-05	0.00295689	missense	NTNG2	GRCh38.p7	9:132226928	GAGCACAACACCACC[A/G]GCCCCGACTGCGGCA	84628
rs781551645	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132193666	TAGGATGAAAAACTC[C/G]CAATTCGTCTCTACC	84628
rs781556504	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132181322	CCTGGGCTCACTTTC[-/T]TTTTTTTTTTTTTTT	84628
rs781578721	snp	C/T			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132165561	GGCTGTTTCTCAGTG[C/T]CTGGCTCTTCATGGT	84628
rs781589888	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132220011	AGCAGGTGATTATCC[A/G]TCTTTTTGACTCTGC	84628
rs781611645	snp	A/G			intron-variant, utr-variant-5-prime	NTNG2	GRCh38.p7	9:132231147	GGTCCCAGGGGAGTC[A/G]GACCAGGGAGGGGCA	84628
rs781625212	snp	A/G	0.000306044	0.0123664	intron-variant	NTNG2	GRCh38.p7	9:132241843	CGGGGGGACCGGGCC[A/G]CCCCCCGTGCTGACC	84628
rs781713380	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132222683	TGGGTTCCTGAGTGC[C/T]CCCTCTCCCACGGCC	84628
rs781714279	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132194716	CACCCTGAGGTTGCA[C/T]AGGGGCCTGAGGACA	84628
rs781714643	snp	C/T			upstream-variant-2KB	NTNG2	GRCh38.p7	9:132160159	GGTAGAGGCACACAA[C/T]GGCCCTGTTTTTTGA	84628
rs781736031	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132188123	GGGTGGGGCTAGCTC[A/G]GCTGCCTTTCCTTGC	84628
rs781737333	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132208980	TCGTTCTCACTGTGC[C/T]TCTGAGGCTTATGGC	84628
rs796069277	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132174900	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	84628
rs796098872	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132170156	GGACCCAGGGGCGGA[C/T]GGCCTTTTCAGATGC	84628
rs796184304	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132187570	GAGCGAGAGGGAGCA[-/AG]AGAGAGAGAGAGAGA	84628
rs796185132	in-del	-/AAAAAAAAAAAAAA			intron-variant	NTNG2	GRCh38.p7	9:132213348	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]GAAGGACTTGAGAGG	84628
rs796185350	in-del	-/CA			intron-variant	NTNG2	GRCh38.p7	9:132210901	ATGTACCCGCCAAGT[-/CA]CACACACACGCAGCC	84628
rs796244300	snp	C/T			utr-variant-3-prime, missense	NTNG2	GRCh38.p7	9:132242389	TCTTTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT	84628
rs796264810	snp	G/T			intron-variant	NTNG2	GRCh38.p7	9:132213258	ACTTGGGAGGCGGAG[G/T]TTAAAGTGAGCTGAG	84628
rs796281202	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132182042	TCCCCCAGCACACCC[C/T]GGCAGCCCAGAGAAG	84628
rs796285363	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132185377	GAGGCAGCTACCAAG[A/C]GCCCCAGCCAGGGGG	84628
rs796340134	in-del	-/AA			intron-variant	NTNG2	GRCh38.p7	9:132178981	AAAAAAAAAAAAAAA[-/AA]CTACTGATGAGGCAC	84628
rs796390901	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132174097	ACAGATAGGCAGGCC[A/G]CACCATGCTGCGGAT	84628
rs796458531	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132228559	ACCATCACACCCTCC[-/T]TTTTTTTTTTTCTTA	84628
rs796471853	in-del	GG/T			intron-variant	NTNG2	GRCh38.p7	9:132215087	AGAGATTGGGGGGGG[GG/T]GTCTCACTTTCTTGC	84628
rs796504172	in-del	-/G			intron-variant	NTNG2	GRCh38.p7	9:132215488	GGGAGGCTGAGGCAG[-/G]ATAATTGCTTGAACC	84628
rs796506473	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132219588	AAAAAAAAAAAAAAA[-/AG]AAAGAAAGAAAGAAA	84628
rs796525463	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132175801	CCTCAGTTTCCCCAA[A/C]TGAGCAGCCGGGGAA	84628
rs796536745	snp	A/G			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132209255	CTATGAGAAACTGCC[A/G]GGCCGTCTTCCAGCG	84628
rs796568895	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132216808	GAGCCCAGACTGCCC[A/G]CCCAGGTCCAGATCC	84628
rs796588057	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132213700	ATGAAAAATGTTTTT[-/T]CCCAAAACAAAAGAA	84628
rs796612517	snp	C/T			intron-variant, downstream-variant-500B	NTNG2	GRCh38.p7	9:132237580	CTGTTCCCCATCCGC[C/T]GCTGGAAAAAGACGG	84628
rs796647556	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132181322	TCCTGGGCTCACTTT[C/T]TTTTTTTTTTTTTTT	84628
rs796656648	snp	A/T			intron-variant	NTNG2	GRCh38.p7	9:132173710	CGGATGGATGGACAG[A/T]CGGACAGACAGGCAG	84628
rs796674543	snp	C/G			intron-variant	NTNG2	GRCh38.p7	9:132210657	CAGCTCTGTGGCTTG[C/G]TGGGCCTCACCAGCT	84628
rs796684256	in-del	-/AG			intron-variant	NTNG2	GRCh38.p7	9:132189418	ATTGGCTTAAAAAAA[-/AG]GTATCATCTCCTGGT	84628
rs796717109	snp	A/C			intron-variant	NTNG2	GRCh38.p7	9:132196856	CAAGTTCCTGCCTCC[A/C]GTACTTCTGTCCAAT	84628
rs796744045	in-del	-/GG			intron-variant	NTNG2	GRCh38.p7	9:132215079	TTTTTGTAGAGATTG[-/GG]GGGGGGGGTCTCACT	84628
rs796820404	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132175169	ACAGAGAGGAGACAG[C/T]CCACTCCCCCTGCCC	84628
rs796830385	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132234026	TGAGGTAGAGCTATC[-/T]TTTTTTTTTTTTTTT	84628
rs796902319	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132195578	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	84628
rs796949163	snp	A/G			intron-variant	NTNG2	GRCh38.p7	9:132195340	TTGAGACAAAGTCTC[A/G]CTCTGTCGCCCAGGC	84628
rs796958155	snp	C/T			intron-variant	NTNG2	GRCh38.p7	9:132188397	GCAACAGCGTCCTTT[C/T]CCTTTTGGGTGAAGG	84628
rs797012991	in-del	-/T			intron-variant	NTNG2	GRCh38.p7	9:132214888	AATTTTTTTTTTTTT[-/T]AGAGACAGGGTCTTG	84628

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