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

RNF126

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs563608344	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648548	CCGAGCCTTCAAGGG[A/C]AGGCTACTCCACAGC	55658
rs563626827	snp	A/G	0.0209421	0.100162	intron-variant	RNF126	GRCh38.p7	19:651144	TCTGTTCCACCAGGA[A/G]CAGGGCCCAGCGACG	55658
rs563639427	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:647639	GGTCATCCTCATGGT[C/T]CCGAGCCCCCCTACT	55658
rs563734716	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650663	AATGGCACGACCTCG[A/G]CTGACTGCAACCTCT	55658
rs563935193	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647890	TGAACGTTTAGAGGG[C/T]GAGGTTAGACAGAGG	55658
rs564037915	in-del	-/G	0.00755907	0.0610114	intron-variant	RNF126	GRCh38.p7	19:653116	GAGCCCCTCCGACCT[-/G]GCCCCACCGTGACGG	55658
rs564175573	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661848	GTGGGGAGTCCAGAC[C/T]CCTCCACCTCCTGCG	55658
rs564189987	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660473	CCAGGTGTCTCAGCA[A/G]CAGCAGTGCCGCCCC	55658
rs564202023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655639	GCCTGCTGGGAGCCC[A/G]GAAGTCCCCCAGATG	55658
rs564204454	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660855	CGGAGAAGTTCTGAC[A/G]CTGCCATGCTGTCTA	55658
rs564291475	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661357	GCCCTGCAACTCACC[A/C]AGGCTGGCGGGCTGT	55658
rs564333340	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:657330	ACTGGCTTTCTGTCG[A/G]GCTCCCGGGTTCCCG	55658
rs564394982	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:653024	GGTGGCTCCCAACCC[A/G]TGGGTCCTGGAGGGC	55658
rs564396852	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657669	ATATCTGAAATCCGG[A/G]TGCCATCGAGGACGC	55658
rs564410746	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662009	GTCAGCCTGGCGAAG[A/G]GCAACACGGGTTAAA	55658
rs564445402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652404	GGAATTGTCCTTGGC[A/G]CTGCTTCCCACCCGC	55658
rs564641674	snp	A/G	0.0252325	0.109451	intron-variant	RNF126	GRCh38.p7	19:650168	GCTGGGGATGGGGAC[A/G]GGCACCCCCACCCAC	55658
rs564742677	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652541	AATGTGGGTAGGGCC[C/T]CCGTGGCCCCTTCCC	55658
rs564755065	snp	A/C/G	8.59882e-05	0.00655643	intron-variant	RNF126	GRCh38.p7	19:649773	GAAGGTGGGGTTCAA[A/C/G]TGGCTGACGGGCAGC	55658
rs564782804	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:648622	CGTGTGTGTGTCCCC[C/T]GGGCTGCCAGAGGGG	55658
rs564852540	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:654335	TCAGCCCACGCCCCA[C/T]GAATTCTCGGCACGC	55658
rs565000848	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:651894	CCTCGGGGGCTCAGG[A/C]CCGTGCAGTCTGCTG	55658
rs565167585	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654084	AAGCGGGGGTCTGGC[A/G]TGCAGTGCCCAAGGG	55658
rs565310081	snp	C/G	0.0123036	0.0774623	intron-variant	RNF126	GRCh38.p7	19:648332	TTAGAGGCGGGAGGG[C/G]CGCGGTCGGGGTGGG	55658
rs565324967	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF126	GRCh38.p7	19:663572	AGGCGCCCTCTCCCC[C/T]GCCCGCTGCCCGGTG	55658
rs565339627	snp	A/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657417	CCCGACCTGGCCACA[A/T]ACACACTCATCTGCC	55658
rs565480669	snp	C/T	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:658950	GCACCGGCATCTGCC[C/T]GAGGCAGACCCCAGC	55658
rs565539285	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657747	CTCTCAGGCCCCCGG[C/G]CAGCCCCTCCAGGGC	55658
rs565910960	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:652586	CACCAGATTAGCCGC[C/T]GAGGCTGAGGGAGGT	55658
rs565935604	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647669	TCCGGGTCGTGGAGG[C/T]GGCCGAGGGGGAGGC	55658
rs566057866	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661631	GCCCCAACTCTAGCA[A/C]TCGCTCCTCCTCTGT	55658
rs566322132	in-del	-/G	0.423311	0.180176	intron-variant	RNF126	GRCh38.p7	19:648345	GGCCGCGGTCGGGGT[-/G]GGGGGGCGGGTGGGC	55658
rs566488277	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:665144	CCAGCCTTCACGCTC[C/T]GCAAGTGCAGGAGGA	55658
rs566597351	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660129	CTGAGCCCCCGACCG[A/C]AAGTGTGGCTCCCCG	55658
rs566614392	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:656280	GCTTGAACCTGGGAG[A/G]TGGAGGCTGCAGTGA	55658
rs566660025	snp	C/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655752	TCACATGGCCAGAAC[C/T]GGCAGGTGAGAGTTC	55658
rs566696965	snp	A/G	0.000253968	0.0112659	intron-variant	RNF126	GRCh38.p7	19:661433	GGAAGAGGCAAGAGC[A/G]AGACCCCTGGGAGAC	55658
rs566723487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652449	TTGGTGCCGTAACCC[A/G]CTGCTGCTTCCCTCG	55658
rs566742801	snp	A/C	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:659084	CCGTTCCGGAGAACC[A/C]AGCTGTGCAGAGCCG	55658
rs566974599	snp	A/G	5.41815e-05	0.00520459	missense	RNF126	GRCh38.p7	19:648132	CCGACGTGGGCTCAC[A/G]AGTTGCTTGTGGCGT	55658
rs566996381	snp	C/G/T	0.000227454	0.0106619	intron-variant	RNF126	GRCh38.p7	19:652182	AGGCTGGCGCTCGGG[C/G/T]CCCCGAGCAAGGCTG	55658
rs567035727	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652068	ATCCAAGAAACCAAC[C/G]AAGCAGCGTGGGCCG	55658
rs567036927	snp	C/T	5.25555e-05	0.00512591	missense	RNF126	GRCh38.p7	19:648434	AGGGCAGCTGCCGCA[C/T]ACGCTCACCCAGCGC	55658
rs567109038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648807	AACCCTGTCTCTACT[A/G]AAAATACAAGTATGA	55658
rs567619548	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653093	CCTTTGGTGGCTCCC[A/G]GCGATCTGAGCCCCT	55658
rs567743508	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658458	GAGACCCCAGGGAGA[A/G]TCATGGTGCAGTGCT	55658
rs567780693	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660929	CCTTGGGATCACCCG[C/T]GGGGTGGACACGGGC	55658
rs567831066	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653344	CACGCTGGCCACACC[C/T]CTGCAAGACCCCATC	55658
rs567851796	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662531	GCGGCCAGGGCTCCA[A/C]GAGGCGAGCCTGCAG	55658
rs567969824	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661396	CAGCCTCTCCTGCCA[A/C]GGCCAGTGGGGACAG	55658
rs568030481	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:656808	GTGTCGGGATTGGGA[C/G/T]GCCCCACGTAAACAC	55658
rs568051579	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656493	GTCTCTACTAAAAAT[A/C]CAAAAATTAGCTGGG	55658
rs568239238	snp	A/G	5.64988e-05	0.00531471	intron-variant	RNF126	GRCh38.p7	19:652891	GATATAATCCTGCAG[A/G]AGAGAACAGGAGGCC	55658
rs568287434	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647289	GCCCTGGCGCTTTAA[C/T]GCTGGTGTTTCTGGT	55658
rs568320932	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650914	CTTTTTAAAAATTAG[A/C]GATGGGGCCTCCCTA	55658
rs568331209	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656522	GGCACGGTGGTGGGT[A/G]CCTGTAATCCCAGCT	55658
rs568346474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655714	AGACCCCAGAGAAAC[A/G]AAGACACCTGCCCAC	55658
rs568672814	in-del	-/CC	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:657993	CTGGTGAAGGAGCTG[-/CC]CCCCACCTTCTCCGG	55658
rs568699160	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653970	GACCCCAGGCTCTGG[A/G]GATGCAGGTTGCACC	55658
rs569027845	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:660562	GTTGTGGCTGGGGAC[C/T]TTCCCCATTGCCAGA	55658
rs569066097	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	RNF126	GRCh38.p7	19:665001	AGCCTCCTTCCAGTC[C/G]TCTTTGCAGCAGCGC	55658
rs569152546	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime	RNF126	GRCh38.p7	19:663138	GCCGCCGCCACCTAC[A/T]CCGCGCCGCCCGCCC	55658
rs569291282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653134	CCCACCGTGACGGGC[A/G]TCACCAGCGTCATCA	55658
rs569411840	snp	C/T	9.25112e-05	0.00680052	intron-variant	RNF126	GRCh38.p7	19:648504	TGCGGGAGTGTGCAG[C/T]TGCGGTCACAGCGGG	55658
rs569436579	snp	C/T	0.00358779	0.0422022	intron-variant	RNF126	GRCh38.p7	19:651526	ATGATGCCACGTTTC[C/T]GTGGAACCCGTGCTG	55658
rs569457805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654133	CCCCGCCCACACCAC[A/G]CCGTGCCTGCCTCAC	55658
rs569607421	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651295	CCTGCGACGGCTCCC[C/T]CAGGCTCTGTTCTGG	55658
rs569675451	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF126	GRCh38.p7	19:647695	GAGGCTGGGGGCCCA[C/T]GTGGCCCGTCCTGGC	55658
rs569682312	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651014	AAATACAGCACTGAG[C/G]CACCGTGCCTGGCAA	55658
rs569863722	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:648073	TGGGTGCCGTGTGGC[A/G]CTGGCTGAGGGTGGG	55658
rs569984621	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657533	TCTGCAGCACCCACT[C/G]CAGCGTCGGGGCCTG	55658
rs570163234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662079	ATCCCAGCGTTTTGG[A/G]AGGCTGAGCCAGAAG	55658
rs570171549	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:656771	ACTCTCCCCAGGCGT[C/T]GGTTCTTGGGGTGTG	55658
rs570183461	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:656355	AACAAAAAAAAGAAA[C/G]AAACAAAGAAAAAAA	55658
rs570425130	snp	C/T	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:660949	TGGACACGGGCAGGC[C/T]CCCGCAGCCCTCTCT	55658
rs570498955	snp	A/G	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:660008	GACCTCAGGTGATCC[A/G]TCCACCTCAGCCTCC	55658
rs570500562	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654521	GGTGGCGGGCGCCTG[C/T]AATCCCAGCTACTTG	55658
rs570526763	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF126	GRCh38.p7	19:652688	GCTGTCTGCACAGAG[-/A]AAAGTGCTCCCGGAG	55658
rs570532509	snp	A/T	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:655811	GCAGATGCAAACAGC[A/T]CCAGTGTCCACCCGC	55658
rs570681933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650041	GGACAGGCACCCCCA[C/T]CCACTCACCAGGGGC	55658
rs570844587	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655791	ACAGTTCATCATCGT[C/T]GTCGGCAGATGCAAA	55658
rs570885087	snp	C/T	0.000648418	0.0179941	intron-variant	RNF126	GRCh38.p7	19:652221	GGGAAGCACGAGGGG[C/T]GGGCGACTCACCTCC	55658
rs570944479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:649066	ACCTGCAAAAGCACC[A/G]AGGCCGCGTTTGTCC	55658
rs570951403	snp	A/G	6.31134e-05	0.00561718	synonymous-codon	RNF126	GRCh38.p7	19:648477	GCACACAGGGCACTC[A/G]AGCCCGGAGCCTGCG	55658
rs570990976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:649278	GGGGGGCCGTGCTCC[A/G]GCTGGTGGGCTACTG	55658
rs571350844	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:663819	TCAGGGCGCTGTCTG[A/G]GCCTCACTGGGACCC	55658
rs571609629	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653176	GAGCCCCTCCGACCT[A/G]CCCCACCGTGACGGG	55658
rs571628663	snp	C/T	0.000122551	0.00782689	synonymous-codon	RNF126	GRCh38.p7	19:648182	GGAGGAGGACGATGA[C/T]GACGAGGAGGAGAAG	55658
rs571680044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662575	CCCCCAACCACGCGC[C/T]CGGCGGGGGTCCCCT	55658
rs571744993	snp	C/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:663016	CCTGCGGCGCAGACC[C/T]TGCCGCCCGCCGCCC	55658
rs571807936	snp	G/T	5.40965e-05	0.00520051	intron-variant	RNF126	GRCh38.p7	19:651564	AGCGCCAGAACTTCC[G/T]ACCTCAAGGCGTGGG	55658
rs571934670	snp	A/G	0.00517822	0.0506191	intron-variant	RNF126	GRCh38.p7	19:654044	AGCAAGCAAGATCCC[A/G]GCCTCACCCACTGAC	55658
rs571947269	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:648351	GGTCGGGGTGGGGGG[G/T]CGGGTGGGCGGGGCA	55658
rs571950323	snp	A/T	0.0517044	0.152246	intron-variant	RNF126	GRCh38.p7	19:650151	ACTCACCAGGGACCC[A/T]GGCTGGGGATGGGGA	55658
rs572072863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650394	CCAAGGGCAGGGCCA[A/G]CATCAGCTTCTAGAT	55658
rs572132181	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665270	TTTTCCGTTGGCTCG[A/G]AGCAGACATGAGGAC	55658
rs572249762	snp	C/G	0.000798403	0.0199641	downstream-variant-500B	RNF126	GRCh38.p7	19:647077	ATCCCAGGATGGTGG[C/G]ATCATCAGCAACTGA	55658
rs572378663	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:656595	AGAGGTTGCAGTGAG[C/G]CGAGATCATACCACT	55658
rs572672384	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652537	TGAGAATGTGGGTAG[G/T]GCCCCCGTGGCCCCT	55658
rs572768948	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:649142	TGGAGCCCACGCGGC[C/T]CCCCCGCTCCTGGGT	55658
rs572895485	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658777	CTCGGCCCAGGCCCC[A/G]AACTCTGCCTTCTTC	55658
rs572921390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654881	CTGAGACAGGAGAAT[C/T]GCTTGAACCTAGGAG	55658
rs572924709	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:648735	GCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCAC	55658
rs572984590	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:652133	ATTTCCTCCGCCGTG[C/T]GGGCAGGGAGAGCCG	55658
rs573062021	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659374	GCTCTTCCCCGCCAC[C/T]GTGGGCGGCAGGGCC	55658
rs573115270	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662124	AGGAGTTCAAGACCA[A/G]CCTGGGCAACACAGG	55658
rs573151367	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654580	CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA	55658
rs573275446	snp	A/G	0.000384295	0.0138564	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651643	GCCTTCGTGCCGGCC[A/G]GTGGCCCGCCGCGTG	55658
rs573278470	snp	C/G	0.00358779	0.0422022	downstream-variant-500B	RNF126	GRCh38.p7	19:647507	CGCACGGGCGCAGAA[C/G]GAAAGCCACAGCACC	55658
rs573340057	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF126	GRCh38.p7	19:647783	CTGGGCCCCGTCTTC[C/T]GCCACAAACCATGCA	55658
rs573452050	snp	G/T	0.0119091	0.0762411	intron-variant	RNF126	GRCh38.p7	19:662739	TCCCACCTGGGATCC[G/T]CGCGGCCTCTCGGGT	55658
rs573456223	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:648521	GCGGTCACAGCGGGC[A/G]TGGGGGGCCTGCCGA	55658
rs573464790	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:663887	CCTTGTTTCCAAGAT[A/G]CTCCACGGGCTGACG	55658
rs573515161	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	RNF126	GRCh38.p7	19:663255	CGGGGCGGAGCGGGG[A/G]CGCGGGAGCGGCGAA	55658
rs573907438	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:658586	GGCACGGGCACGTGC[A/G]GCGCCTGCACCCCTT	55658
rs573959082	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651054	CTTTTAAAGATGACA[C/T]TTCCAGCAGGTGAGA	55658
rs574030099	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:658015	CTTCTCCGGGGGCAG[C/G]ACGCACTGGGGGCCC	55658
rs574082017	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:657169	GGCCTGAGGGAGAAG[C/G]TGTCTCCCTCTGAGG	55658
rs574097677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661744	GGGCTTGGACTTCTC[C/T]TACGGGTCAAAGCGT	55658
rs574169842	snp	G/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657587	ACGCCCACCCTAGGG[G/T]TTTCAAAGGTCACCT	55658
rs574344612	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655882	AGACCAGGCCACGGC[A/G]GGGGGGAGGGGGGAT	55658
rs574344930	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655421	AACCTGGGAGGCAGA[A/G]CTTGCAGTGAGCCGA	55658
rs574367049	snp	C/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:651352	ACACGCGTGTGGACA[C/G]CAGTCTCCAGAGCAC	55658
rs574550719	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:652646	CTCTGGCCCCGGCCC[A/G]GCCATCACAGAAGAG	55658
rs574600328	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:658972	GACCCCAGCGCCAGC[C/T]GGCCAGAGAGGGCAG	55658
rs574633533	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:664803	GGGCACCACCACGCC[C/T]GCCTAATTTTTGTAT	55658
rs574753410	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648831	AGTATGAGCCAGGCG[C/T]GGCGGCGGGTGCCTG	55658
rs574827867	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661728	CTGCACTGCTTCTGG[A/G]GGGCTTGGACTTCTC	55658
rs575084052	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	RNF126	GRCh38.p7	19:663427	GCGGGGCGTGCGCGG[A/G]GCGGGGCCGAGGCCC	55658
rs575100297	snp	C/T	0.000895526	0.0211415	intron-variant	RNF126	GRCh38.p7	19:651964	GGCCCTGCTGGGTGC[C/T]GGGTGGGAGGGAGAC	55658
rs575107758	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655554	AACACGCTGGGTAAA[C/G]GCAGCCGGCCAGCCC	55658
rs575148120	snp	C/T	0.00438332	0.0466095	intron-variant	RNF126	GRCh38.p7	19:658768	AGGGCGTGCCTCGGC[C/T]CAGGCCCCGAACTCT	55658
rs575329167	snp	A/G	0.00159617	0.0282053	intron-variant	RNF126	GRCh38.p7	19:659369	CGCCGGCTCTTCCCC[A/G]CCACCGTGGGCGGCA	55658
rs575338904	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659719	CACGCCCCACTCTGG[C/G]TGACGCTCCCTTTGC	55658
rs575413519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:648571	TCCACAGCCTCAGCC[A/G]GAGGCCGCCCCTGAG	55658
rs575589466	snp	C/T	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:658175	CCAGGGTAGGGGGGA[C/T]CCTGCCAGTGCCGGG	55658
rs575615964	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664156	TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCTCGA	55658
rs575700437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653275	GTGGCATTTCCAGGA[C/T]GCTCTGGCAGCCCCG	55658
rs575718375	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:653449	CCAGGGACAGCCGTG[A/G]GTGAGTCCCAAAACC	55658
rs575733551	snp	A/G	0.00127146	0.0251816	utr-variant-3-prime	RNF126	GRCh38.p7	19:647970	CCAAGCCAGGGGGCC[A/G]GTGGGCCGGGCCCGG	55658
rs575890668	snp	A/G	5.62604e-05	0.00530349	intron-variant	RNF126	GRCh38.p7	19:651586	AGGCGTGGGGCCCTC[A/G]CGGCCACCCCCGGGG	55658
rs575933898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:650481	GGAGAGAAGCAGCTT[A/G]ATCTTGGTTCACTGC	55658
rs576003459	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647117	ACTGCCCCGGCCCCC[C/T]GAGCCCGCAGGTCCC	55658
rs576009579	snp	A/G	0.00279162	0.0372561	intron-variant	RNF126	GRCh38.p7	19:653467	GAGTCCCAAAACCAC[A/G]TTCACAGTTCCCCAG	55658
rs576049593	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF126	GRCh38.p7	19:647476	CGACCAGCCTCCCAG[A/C]TTGGCCTTTTCCTGA	55658
rs576175579	snp	A/T	0.0023933	0.0345097	intron-variant	RNF126	GRCh38.p7	19:662263	AGCGCTGCTCCCACC[A/T]CCCCCAAGGTGACAT	55658
rs576235760	snp	C/T	0.00120096	0.0244753	intron-variant	RNF126	GRCh38.p7	19:656911	CAGGGGTTGCCGCCG[C/T]CCGCCCGCCAGCTGA	55658
rs576298524	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652956	CCCCAAGTGTGAGGA[C/T]AGAGGGGCTCCGGAC	55658
rs576318359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:662663	ACCGGGCAATACCCT[C/T]TCTCTGCTCGCCGGG	55658
rs576492600	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661081	GCAAAGACCACAGCG[C/G]CCTGTCACCACAGAG	55658
rs576649153	snp	C/T	0.000399281	0.0141238	missense	RNF126	GRCh38.p7	19:650241	CCACTCACCAGGGGC[C/T]CAGGCTGGGGATGGT	55658
rs576805612	snp	C/T	0.00557542	0.0525036	intron-variant	RNF126	GRCh38.p7	19:661650	CTCCTCCTCTGTGAC[C/T]CAGAGACAGGCGGCT	55658
rs576901788	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:654946	TAACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	55658
rs576903600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:660204	GCCACTCTGCACACA[C/T]GTGCCCACCAGATGC	55658
rs576914090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:655465	CACTCTAGCCCGGGC[A/G]ACAGAGTGACACTCC	55658
rs577099729	snp	C/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:652495	TTTCTCGATAAACCG[C/G]TGCAGACCCCAACAG	55658
rs577138810	snp	C/T	0.00070238	0.0187269	intron-variant	RNF126	GRCh38.p7	19:651563	AAGCGCCAGAACTTC[C/T]GACCTCAAGGCGTGG	55658
rs577389165	snp	G/T	0.0360663	0.129354	upstream-variant-2KB	RNF126	GRCh38.p7	19:664592	ATGAGGCATTGGAGC[G/T]AGACTGTTGAGGAAT	55658
rs577391222	in-del	-/AAAAAAAAA			intron-variant	RNF126	GRCh38.p7	19:654671	AAAAAAAAAAAAAAA[-/AAAAAAAAA]GTGCTGGCCGGGCGC	55658
rs577425572	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659169	GTATCTGGCACAACC[A/G]CAGACACACAGAGCA	55658
rs577427313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653887	GACCACCCCCAGGTA[A/G]CACAGACAAAAACAG	55658
rs577501396	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF126	GRCh38.p7	19:665198	GCCAAACCACGAACT[A/G]GCTGTGTGTCCCTAG	55658
rs577646121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:659837	GGCACAATCTCGGCT[C/T]ACTGCAACCTCCGCC	55658
rs577862798	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF126	GRCh38.p7	19:647617	AGTTTTGTTCTTGAA[C/T]TTTGCTGGTCATCCT	55658
rs577875277	snp	A/G	0.000709723	0.0188244	utr-variant-3-prime	RNF126	GRCh38.p7	19:647873	AAAAATCTTTCCACC[A/G]CTGAACGTTTAGAGG	55658
rs578013229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:653183	TCCGACCTGCCCCAC[C/T]GTGACGGGCGTCACC	55658
rs578069491	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657265	CGTGGCCTGGCACAG[C/T]GCTCGGCCGCTCTGG	55658
rs578079974	snp	A/C	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:657630	CCTCTGCCCTGTCAC[A/C]GAGGACAGCCTGGAC	55658
rs578097717	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649914	CCCACCCACTCACCA[A/G]GGGCCCAGGCTGGGG	55658
rs578111986	snp	A/G	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:653421	TGTCCCAGAGGAGAC[A/G]TGAGGACCCTGCCCA	55658
rs578139476	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651430	ACCCTGAACCGGCAT[A/G]CTTCTGTCTCCGAAG	55658
rs578157558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:651367	GCAGTCTCCAGAGCA[C/T]GTGGGCCTGGCAGGC	55658
rs745339984	snp	A/G	0.00026688	0.0115485	missense, intron-variant	RNF126	GRCh38.p7	19:651624	ACCCTTCCAGCGTGG[A/G]GACGCCTTCGTGCCG	55658
rs745478248	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655841	CACCTCAGAGCACGA[C/T]TCAACCATGGAAAGG	55658
rs745565057	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655145	CCAAACCCCATTTCT[A/G]CAAAAAACAAATTAG	55658
rs745588633	snp	C/G	0.000105014	0.00724543	intron-variant	RNF126	GRCh38.p7	19:648311	AGGGACGGGAGAAGG[C/G]GCAGGTTAGAGGCGG	55658
rs745641231	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664726	GGTTCACTGTAACCT[C/T]CGCCTCCCGGGTTCA	55658
rs745653093	snp	G/T	0.00446925	0.0470601	intron-variant	RNF126	GRCh38.p7	19:648356	GGGTGGGGGGGCGGG[G/T]GGGCGGGGCACTCAC	55658
rs745734878	snp	C/T	9.59923e-05	0.00692726	intron-variant	RNF126	GRCh38.p7	19:649642	GGGCAGCCCAGCCCT[C/T]CCCCAGCAGGCACTC	55658
rs745756255	snp	C/T	0.000124438	0.00788694	intron-variant	RNF126	GRCh38.p7	19:651947	AAGGAGAAAGCAAGA[C/T]GGGCCCTGCTGGGTG	55658
rs745919856	snp	A/G	0.00136705	0.0261086	utr-variant-3-prime	RNF126	GRCh38.p7	19:647949	GACCATGTGGCCCAC[A/G]CCTTCCCAAGCCAGG	55658
rs745990688	snp	A/C	1.85703e-05	0.0030471	intron-variant	RNF126	GRCh38.p7	19:649785	CAAGTGGCTGACGGG[A/C]AGCTGGGGCAGGTGC	55658
rs746006596	snp	A/G	1.99114e-05	0.0031552	intron-variant	RNF126	GRCh38.p7	19:652912	ACAGGAGGCCGGGTC[A/G]CGGTGACGCCGGCAT	55658
rs746190592	in-del	-/C			downstream-variant-500B	RNF126	GRCh38.p7	19:647428	TGCAGGAGGCGCAGA[-/C]CCCCTGGAGACAGGA	55658
rs746227213	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:661670	GACAGGCGGCTTCTC[A/C]TGACTCCCTCCAGCC	55658
rs746295288	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:657957	GGGGCAGCTGCAGGT[A/G]GAAACGCCTGGGCAA	55658
rs746300518	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:650656	GGAGTGCAATGGCAC[A/G]ACCTCGGCTGACTGC	55658
rs746340676	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661002	TCTACCAACGTCCAT[A/G]ATTAAATATTTGTCA	55658
rs746491041	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658698	ACAAGCTGGATGGAC[A/G]AGGCGTGAGCGAAGC	55658
rs746509826	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661030	TCAATCACTGTTCCA[C/T]GCTGGCTCCCTGGCC	55658
rs746528436	snp	G/T	4.31025e-05	0.00464213	missense	RNF126	GRCh38.p7	19:652259	GCCGGCTCTGGTCTG[G/T]GGGAGCTGTGGAGGG	55658
rs746597740	snp	A/C	6.73469e-05	0.00580249	intron-variant	RNF126	GRCh38.p7	19:652332	AGCAGTGCCGGCTAC[A/C]CTGTGCCCCCATGCG	55658
rs746631506	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651243	GAGTGGGGCCCTGCG[A/G]CGGCTCCCCCAGGCT	55658
rs746721458	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650741	GGGATTACAGGCGCC[C/T]ACCGCCATGCCTGGC	55658
rs746809775	snp	C/T	6.33814e-05	0.00562909	missense, intron-variant	RNF126	GRCh38.p7	19:651614	GGGCCCCCTCACCCT[C/T]CCAGCGTGGGGACGC	55658
rs746837620	snp	C/T	2.68886e-05	0.00366655	missense	RNF126	GRCh38.p7	19:648199	ACGAGGAGGAGAAGC[C/T]CACCCCAGTGAGGCC	55658
rs746879840	snp	C/T	1.73354e-05	0.00294404	synonymous-codon	RNF126	GRCh38.p7	19:651844	CAGCGTGAACAGGTG[C/T]TGGTCCACGTGCTGG	55658
rs747113673	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:658837	GGGACTGGAACCCCA[A/C]AGGTGCCCATCCGTG	55658
rs747190492	in-del	-/GGGCGGGTGGGC	0.00469613	0.0482288	intron-variant	RNF126	GRCh38.p7	19:648349	GCGGTCGGGGTGGGG[-/GGGCGGGTGGGC]GGGGCACTCACCTGC	55658
rs747261322	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647338	GTGACACTGCCACCC[C/T]GCTACCTCGCCAGCA	55658
rs747290550	snp	C/T	8.42283e-05	0.00648899	intron-variant	RNF126	GRCh38.p7	19:649770	GTGGAAGGTGGGGTT[C/T]AAGTGGCTGACGGGC	55658
rs747372634	snp	A/G	3.88939e-05	0.0044097	intron-variant	RNF126	GRCh38.p7	19:652904	AGGAGAGAACAGGAG[A/G]CCGGGTCACGGTGAC	55658
rs747390494	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653776	AATCAACTGCTCTCT[A/G]TGAACGACCCAGTCT	55658
rs747399983	snp	C/T	0.000377608	0.0137354	missense, intron-variant	RNF126	GRCh38.p7	19:651680	CGGGCGCGGGGCTGT[C/T]GGGCGCCGTACCGGT	55658
rs747403945	snp	A/G	7.37237e-05	0.00607095	utr-variant-3-prime	RNF126	GRCh38.p7	19:647908	GGTTAGACAGAGGAC[A/G]GGGAGGCTGGGGACG	55658
rs747476539	in-del	-/TCA			intron-variant	RNF126	GRCh38.p7	19:655781	TCACGGCAGCACAGT[-/TCA]TCATCGTCGTCGGCA	55658
rs747576239	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:657118	CCACCATCTCTCCTG[-/C]CTGGGTGCATCCACA	55658
rs747645636	snp	C/T	0.000158877	0.00891142	missense	RNF126	GRCh38.p7	19:648455	CACCCAGCGCGTAGT[C/T]GTCCTTGCACACAGG	55658
rs747673387	snp	A/G	0.000262398	0.0114512	intron-variant	RNF126	GRCh38.p7	19:648517	AGCTGCGGTCACAGC[A/G]GGCGTGGGGGGCCTG	55658
rs747789087	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661774	TAGCAACAGCCGGGC[A/G]GCTACGTACACAGCA	55658
rs747910372	snp	A/G	5.91804e-05	0.00543936	utr-variant-3-prime	RNF126	GRCh38.p7	19:648122	TTCCCGACGGCCGAC[A/G]TGGGCTCACGAGTTG	55658
rs747962896	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:657852	TGAGCCTCTGCTGGC[C/T]GACGGTGGGAGGGGC	55658
rs748050897	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:657129	TCCTGCTGGGTGCAT[C/T]CACAAGGTCAGGCAG	55658
rs748143806	snp	A/G	2.49355e-05	0.00353088	missense	RNF126	GRCh38.p7	19:648186	GAGGACGATGACGAC[A/G]AGGAGGAGAAGCTCA	55658
rs748264977	snp	C/G	1.68584e-05	0.00290326	synonymous-codon	RNF126	GRCh38.p7	19:648904	CTCCTCAGTGACGGG[C/G]ACGGTGGGGAGGGCC	55658
rs748277518	snp	A/G	0.000418031	0.0144513	intron-variant	RNF126	GRCh38.p7	19:652202	GAGCAAGGCTGACAC[A/G]ATCGGGAAGCACGAG	55658
rs748329784	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660144	CAAGTGTGGCTCCCC[A/G]CTCAGGACACCCTCA	55658
rs748417587	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:659038	CCGATCACAACGCCA[C/G]GCTCCATGTTCACAG	55658
rs748537465	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647809	ATGCATGGCCGCCAC[A/G]TGAGCTCAAACGTCC	55658
rs748576944	snp	A/T	1.77871e-05	0.00298215	intron-variant	RNF126	GRCh38.p7	19:649007	GAGAGTGCCGGGAGC[A/T]CCTCGGGGGCCCGGC	55658
rs748606659	snp	C/T	6.70264e-05	0.00578867	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651631	CAGCGTGGGGACGCC[C/T]TCGTGCCGGCCGGTG	55658
rs748627386	snp	A/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647446	CCTGGAGACAGGACC[A/G]GACTCTGCAGAGCCC	55658
rs748648424	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654401	TAATCCTGGCACTTC[A/G]GGAGGCCGAGGCGGG	55658
rs748715167	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:653839	CTCACACGGCACGTG[A/T]CATCACGCCAGGGGC	55658
rs748772018	snp	C/T	0.000666481	0.0182427	missense, intron-variant	RNF126	GRCh38.p7	19:651669	GCGTGGTGAGGCGGG[C/T]GCGGGGCTGTCGGGC	55658
rs748778583	snp	A/G	5.01706e-05	0.00500827	intron-variant	RNF126	GRCh38.p7	19:648364	GGGCGGGTGGGCGGG[A/G]CACTCACCTGCTCCA	55658
rs748888015	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664388	CTCATTGAGCAACTA[C/T]TGCACACCAGACCCT	55658
rs748924027	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:653883	CCAAGACCACCCCCA[C/G]GTAACACAGACAAAA	55658
rs748977851	snp	A/C/G			intron-variant	RNF126	GRCh38.p7	19:662756	GCGGCCTCTCGGGTC[A/C/G]GGAACGCCGCGGATG	55658
rs749023121	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:657293	TGGTCCCCATGTGCC[A/G]AGCTCAGCCCCTCTG	55658
rs749078941	snp	A/G	3.50877e-05	0.00418839	intron-variant	RNF126	GRCh38.p7	19:652203	AGCAAGGCTGACACG[A/G]TCGGGAAGCACGAGG	55658
rs749194384	snp	A/G	1.74054e-05	0.00294998	synonymous-codon	RNF126	GRCh38.p7	19:650290	GTTGACGAGCTGCTG[A/G]ATGATCCTGGAAAAG	55658
rs749307687	snp	A/G	4.83349e-05	0.0049158	missense	RNF126	GRCh38.p7	19:648177	GAGCTGGAGGAGGAC[A/G]ATGACGACGAGGAGG	55658
rs749420451	snp	C/T	0.00018659	0.00965714	utr-variant-3-prime	RNF126	GRCh38.p7	19:648118	TGCTTTCCCGACGGC[C/T]GACGTGGGCTCACGA	55658
rs749523308	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660940	CCCGCGGGGTGGACA[C/T]GGGCAGGCCCCCGCA	55658
rs749626571	snp	C/T	7.88343e-05	0.00627781	synonymous-codon	RNF126	GRCh38.p7	19:648892	CATACCTACGTGCTC[C/T]TCAGTGACGGGGACG	55658
rs749660637	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:660294	CTGCCCAGCAGAGAA[G/T]GACCCAGCTGCGCGG	55658
rs749702703	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659204	GCGGCCAGAGACAGA[C/T]CCAGGCCGTCTTCTG	55658
rs749741459	snp	C/T	4.34414e-05	0.00466035	missense	RNF126	GRCh38.p7	19:652265	TCTGGTCTGTGGGAG[C/T]TGTGGAGGGGGCAGA	55658
rs749822416	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647898	TAGAGGGTGAGGTTA[A/G]ACAGAGGACGGGGAG	55658
rs749944512	snp	C/T	7.50779e-05	0.00612644	missense	RNF126	GRCh38.p7	19:649731	GCGTAGTCCATAGGG[C/T]TTGAGTGCAGGACTC	55658
rs749990025	in-del	-/GAGCTG	2.39725e-05	0.00346203	cds-indel	RNF126	GRCh38.p7	19:648161	TTCTCGTTGCTGGGC[-/GAGCTG]GAGCTGGAGGAGGAC	55658
rs749992842	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664465	AGCGTGGAACTCAAG[A/G]GTGACTCTGGCTCTG	55658
rs750019608	in-del	-/C	0.000134336	0.00819452	intron-variant	RNF126	GRCh38.p7	19:650225	GGACAGGCACCCCCA[-/C]CCACTCACCAGGGGC	55658
rs750117113	snp	A/C	3.84756e-05	0.00438592	utr-variant-3-prime	RNF126	GRCh38.p7	19:648081	GTGTGGCGCTGGCTG[A/C]GGGTGGGTGGGAAAG	55658
rs750181157	snp	A/G	0.000156246	0.00883734	missense	RNF126	GRCh38.p7	19:648437	GCAGCTGCCGCACAC[A/G]CTCACCCAGCGCGTA	55658
rs750221836	snp	C/T	5.3817e-05	0.00518706	missense	RNF126	GRCh38.p7	19:651747	GGTCCCTGCCGTCGT[C/T]AGCCTGCGCCCCAGG	55658
rs750279942	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649302	GCTACTGTGAGGGTC[A/G]GGTCCTGCCAGTGAC	55658
rs750342616	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660841	GGTCCTGCCACGTAC[A/G]GAGAAGTTCTGACAC	55658
rs750383995	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659985	AGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	55658
rs750443570	snp	A/G	0.000158684	0.008906	synonymous-codon	RNF126	GRCh38.p7	19:650275	GGGCGTGATGATGCC[A/G]TTGACGAGCTGCTGG	55658
rs750480197	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:655509	AGAAAAGTGGGGGGG[-/G]AAAGGACGTGTACAG	55658
rs750487989	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654246	ACCGTGAGGGGAGAG[C/T]GAAGAGGCACCATCT	55658
rs750500020	snp	A/C/T	0.000141343	0.00840544	intron-variant	RNF126	GRCh38.p7	19:652201	CGAGCAAGGCTGACA[A/C/T]GATCGGGAAGCACGA	55658
rs750535662	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647153	CTTGCCAGCTGTGCC[C/T]GAGCTGGCTGCACCC	55658
rs750609946	in-del	-/TGCCCGG			upstream-variant-2KB	RNF126	GRCh38.p7	19:663579	CTCTCCCCCGCCCGC[-/TGCCCGG]TGCAGCGCTCTCCCG	55658
rs750644853	snp	C/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:663881	TTGTGGCCTTGTTTC[C/G]AAGATGCTCCACGGG	55658
rs750721379	snp	A/G	6.71975e-05	0.00579605	intron-variant	RNF126	GRCh38.p7	19:650323	AGCGCCAGTCACGGG[A/G]TGAGGCCGCCCCACG	55658
rs750816702	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651939	CAAAGACAAAGGAGA[A/G]AGCAAGACGGGCCCT	55658
rs750986115	snp	C/G	1.71161e-05	0.00292536	missense	RNF126	GRCh38.p7	19:651823	AAACTGTCCGTAGCC[C/G]TGCGGCAGCGTGAAC	55658
rs750991980	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651155	AGGAGCAGGGCCCAG[C/T]GACGGCTCCCCCAGG	55658
rs751070691	snp	G/T	2.98085e-05	0.00386049	intron-variant	RNF126	GRCh38.p7	19:648876	CGGGAGGCTGAGCTC[G/T]CATACCTACGTGCTC	55658
rs751343232	snp	C/T	5.50585e-05	0.00524654	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651652	CCGGCCGGTGGCCCG[C/T]CGCGTGGTGAGGCGG	55658
rs751376878	snp	A/G/T	5.45165e-05	0.00522071	missense	RNF126	GRCh38.p7	19:652877	TCGCATCTTGGACAG[A/G/T]TATAATCCTGCAGGA	55658
rs751428279	snp	C/T	5.64839e-05	0.00531401	intron-variant	RNF126	GRCh38.p7	19:652805	GGCTCTTCCAGCCTC[C/T]TCAACAGGGGGCTGC	55658
rs751438805	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:652660	GGCCATCACAGAAGA[-/G]GAACGGCACGCTGCT	55658
rs751517619	snp	C/T	0.0001998	0.00999301	missense	RNF126	GRCh38.p7	19:651698	GCGCCGTACCGGTGC[C/T]GGGACGGATGGTCTC	55658
rs751599993	snp	A/G	0.000106106	0.00728299	missense	RNF126	GRCh38.p7	19:648431	TGCAGGGCAGCTGCC[A/G]CACACGCTCACCCAG	55658
rs751616027	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:648800	ATGGTGAAACCCTGT[C/T]TCTACTGAAAATACA	55658
rs751655593	snp	A/C	1.68937e-05	0.0029063	intron-variant	RNF126	GRCh38.p7	19:651942	AGACAAAGGAGAAAG[A/C]AAGACGGGCCCTGCT	55658
rs751688267	in-del	-/AAAG			intron-variant	RNF126	GRCh38.p7	19:654995	AGTGCTTACAACTCA[-/AAAG]AAAGAAAGAAAGAAA	55658
rs751800785	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655527	AGGACGTGTACAGGA[C/T]ATGCCTCCAAAAACA	55658
rs751820418	snp	C/T	7.15333e-05	0.0059801	utr-variant-3-prime	RNF126	GRCh38.p7	19:648101	GGGTGGGAAAGGCCC[C/T]GTGCTTTCCCGACGG	55658
rs751976024	snp	C/T	5.3736e-05	0.00518316	missense	RNF126	GRCh38.p7	19:650259	GGCTGGGGATGGTGG[C/T]GGGCGTGATGATGCC	55658
rs751986332	snp	A/C			upstream-variant-2KB	RNF126	GRCh38.p7	19:663986	AACGGTATCATCACC[A/C]AGCACAGGCCAGGAT	55658
rs752277190	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652493	GGTTTCTCGATAAAC[C/T]GGTGCAGACCCCAAC	55658
rs752285591	snp	C/T	1.75139e-05	0.00295916	missense	RNF126	GRCh38.p7	19:651756	CGTCGTCAGCCTGCG[C/T]CCCAGGAGGGAACGT	55658
rs752563912	in-del	-/AG/G	1.85962e-05	0.00304922	intron-variant	RNF126	GRCh38.p7	19:652811	CCAGCCTCTTCAACA[-/AG/G]GGGGGCTGCATTACC	55658
rs752638557	snp	A/C	9.75163e-05	0.00698202	intron-variant	RNF126	GRCh38.p7	19:652788	ACAGCTGAGGCCCGG[A/C]TGGCTCTTCCAGCCT	55658
rs752948798	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:651029	CCACCGTGCCTGGCA[A/C]AATTAGCCACTTTTA	55658
rs752982210	snp	A/T	1.72098e-05	0.00293336	synonymous-codon	RNF126	GRCh38.p7	19:649745	GTTTGAGTGCAGGAC[A/T]CCCCTGGAGGTGGAA	55658
rs753018657	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655618	CGAGATGCAAGACCC[C/T]GTCAGGCCTGCTGGG	55658
rs753033589	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656511	AAAATTAGCTGGGCA[C/T]GGTGGTGGGTGCCTG	55658
rs753091933	snp	G/T	7.32467e-05	0.00605128	intron-variant	RNF126	GRCh38.p7	19:652194	GGGGCCCCGAGCAAG[G/T]CTGACACGATCGGGA	55658
rs753147272	snp	C/G	0.000110635	0.00743676	intron-variant	RNF126	GRCh38.p7	19:651930	GCTAGGGCACAAAGA[C/G]AAAGGAGAAAGCAAG	55658
rs753213109	snp	A/G	0.000451569	0.0150193	utr-variant-3-prime	RNF126	GRCh38.p7	19:647894	CGTTTAGAGGGTGAG[A/G]TTAGACAGAGGACGG	55658
rs753259863	snp	A/G	0.000842105	0.0205023	intron-variant	RNF126	GRCh38.p7	19:663009	CCTCAGGCCTGCGGC[A/G]CAGACCCTGCCGCCC	55658
rs753315813	snp	A/C	0.000330502	0.0128508	intron-variant	RNF126	GRCh38.p7	19:650226	GACAGGCACCCCCAC[A/C]CACTCACCAGGGGCC	55658
rs753358594	snp	C/T	4.71143e-05	0.00485334	synonymous-codon	RNF126	GRCh38.p7	19:651718	CGGATGGTCTCTCTC[C/T]CGCCGGCTCTCAGGG	55658
rs753396134	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649672	CTGGGCCGTGGCCAC[A/G]CTGTACCTGTGTGAT	55658
rs753403508	snp	C/T	0.00015804	0.00888792	utr-variant-3-prime	RNF126	GRCh38.p7	19:648085	GGCGCTGGCTGAGGG[C/T]GGGTGGGAAAGGCCC	55658
rs753497371	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660699	CACTGGCACCATCAC[A/G]GCTCACCGCAGCCTC	55658
rs753514657	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652725	ACACCAGGGCCTGAC[A/G]GCCCCACACTCGGCG	55658
rs753517011	in-del	-/G	1.68766e-05	0.00290483	frameshift-variant	RNF126	GRCh38.p7	19:652272	TGTGGGAGCTGTGGA[-/G]GGGGCAGAACCATTT	55658
rs753608761	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652509	GGTGCAGACCCCAAC[A/G]GCCTCCTAAGCGTGA	55658
rs753680015	in-del	-/AGA	2.57593e-05	0.00358873	cds-indel	RNF126	GRCh38.p7	19:648192	ATGACGACGAGGAGG[-/AGA]AGAAGCTCACCCCAG	55658
rs753691403	snp	A/G	0.000110199	0.00742208	intron-variant	RNF126	GRCh38.p7	19:648509	GAGTGTGCAGCTGCG[A/G]TCACAGCGGGCGTGG	55658
rs753719057	snp	C/T	0.000127918	0.00799642	synonymous-codon	RNF126	GRCh38.p7	19:652245	CACCTCCAACGGTGG[C/T]CGGCTCTGGTCTGTG	55658
rs753791752	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:658620	TCCCGCCCTCAGCAG[C/T]TGCCACCACATCCCA	55658
rs753873207	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:662062	GGTGGCTCACACCTG[C/T]AATCCCAGCGTTTTG	55658
rs753899567	snp	A/C	0.000222775	0.0105517	intron-variant	RNF126	GRCh38.p7	19:650334	CGGGGTGAGGCCGCC[A/C]CACGCACAGGAGAGG	55658
rs753955560	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660187	AGAGCGGCCAGGTGC[C/T]GGCCACTCTGCACAC	55658
rs754020768	in-del	-/CTCT			intron-variant	RNF126	GRCh38.p7	19:661573	GAGAGGAAACCACAC[-/CTCT]CTCTTTCCACTCCTG	55658
rs754049287	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:661450	GACCCCTGGGAGACA[C/G]AGGAGTAAGGCAAGG	55658
rs754159720	snp	A/G	6.23111e-05	0.00558137	synonymous-codon	RNF126	GRCh38.p7	19:648263	GCTTTTTCGGCAGAC[A/G]GGGCAGCTGTCGTGC	55658
rs754161981	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651485	CTGGAGGGCCTGGCC[A/G]GGCGGCCTCTCCAGA	55658
rs754168349	snp	A/G	0.000129634	0.00804987	intron-variant	RNF126	GRCh38.p7	19:648334	AGAGGCGGGAGGGCC[A/G]CGGTCGGGGTGGGGG	55658
rs754174513	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651112	AGGAGTAGGGCCCTG[C/T]GACGGCTCCCCCAGG	55658
rs754247452	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654336	CAGCCCACGCCCCAC[A/G]AATTCTCGGCACGCT	55658
rs754264696	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656637	TGGGCCACAGAGTGA[A/G]ACCGTGTCAGAAAAA	55658
rs754402748	snp	C/G	3.48329e-05	0.00417316	intron-variant	RNF126	GRCh38.p7	19:648992	TGAAAGACAAGAGGC[C/G]AGAGTGCCGGGAGCT	55658
rs754431578	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:655794	GTTCATCATCGTCGT[C/G]GGCAGATGCAAACAG	55658
rs754432485	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652022	AGCCTGCCCCGCTGG[C/T]GTGAGATGCCTCGGT	55658
rs754512977	snp	C/T	0.000139603	0.00835356	missense	RNF126	GRCh38.p7	19:651719	GGATGGTCTCTCTCC[C/T]GCCGGCTCTCAGGGT	55658
rs754586417	snp	A/C	0.000255363	0.0112967	missense	RNF126	GRCh38.p7	19:663093	CAGTGGCAGAAGTAC[A/C]GTCCGGGATGCGGCG	55658
rs754682446	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:657782	GAAGGCCGGAACCGA[C/G]GCTCTGGTCACGAAG	55658
rs754692298	snp	C/T	5.1971e-05	0.00509733	missense	RNF126	GRCh38.p7	19:648449	CACGCTCACCCAGCG[C/T]GTAGTCGTCCTTGCA	55658
rs754706173	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:656928	CGCCCGCCAGCTGAC[C/G]GGGAGCCCAGGGCCG	55658
rs754725925	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:658369	GACTGACAGTGACCA[C/G]GGCAGGCAGGCCCCT	55658
rs754875424	in-del	-/GGGGGGGGGG	0.000797766	0.0199561	intron-variant	RNF126	GRCh38.p7	19:648339	GGGAGGGCCGCGGTC[-/GGGGGGGGGG]GGGGTGGGGGGGCGG	55658
rs754956085	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:657337	TTCTGTCGGGCTCCC[A/G]GGTTCCCGTCTCAGT	55658
rs755001423	snp	C/T	1.73192e-05	0.00294267	missense	RNF126	GRCh38.p7	19:648274	AGACGGGGCAGCTGT[C/T]GTGCTTTGTGGGGAC	55658
rs755061836	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:660029	CTCAGCCTCCCAAAG[C/G]GATGGGACCACAGGC	55658
rs755134546	snp	C/T	3.43737e-05	0.00414556	synonymous-codon	RNF126	GRCh38.p7	19:651829	TCCGTAGCCCTGCGG[C/T]AGCGTGAACAGGTGC	55658
rs755404177	snp	A/G	7.60081e-05	0.00616427	missense	RNF126	GRCh38.p7	19:649738	CCATAGGGTTTGAGT[A/G]CAGGACTCCCCTGGA	55658
rs755439775	snp	A/G	0.00011115	0.00745404	intron-variant	RNF126	GRCh38.p7	19:651883	GGGGGGCGTGACCTC[A/G]GGGGCTCAGGCCCGT	55658
rs755446264	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664027	GTTAGTTCTGGCCCA[A/G]TCATGCATGCATTTC	55658
rs755524924	snp	A/G	6.29109e-05	0.00560816	intron-variant	RNF126	GRCh38.p7	19:648994	AAAGACAAGAGGCGA[A/G]AGTGCCGGGAGCTCC	55658
rs755539569	snp	C/T			utr-variant-3-prime	RNF126	GRCh38.p7	19:647684	CGGCCGAGGGGGAGG[C/T]TGGGGGCCCACGTGG	55658
rs755643852	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664537	TGGAACCAGGGCTGA[A/G]GGATGAATAGGATTT	55658
rs755780823	snp	C/G/T	5.17964e-05	0.00508881	missense	RNF126	GRCh38.p7	19:651711	GCCGGGACGGATGGT[C/G/T]TCTCTCCCGCCGGCT	55658
rs755798297	in-del	-/GAG	2.48278e-05	0.00352325	cds-indel	RNF126	GRCh38.p7	19:648186	GAGGACGATGACGAC[-/GAG]GAGGAGAAGCTCACC	55658
rs755840048	snp	A/G	5.16489e-05	0.00508151	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651664	CCGCCGCGTGGTGAG[A/G]CGGGCGCGGGGCTGT	55658
rs756016388	snp	A/G	5.15903e-05	0.00507863	synonymous-codon	RNF126	GRCh38.p7	19:648446	GCACACGCTCACCCA[A/G]CGCGTAGTCGTCCTT	55658
rs756041150	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:657897	TCCAGCCGCCCTCCT[A/C]CTCCAAGGGCACAGC	55658
rs756162145	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:661287	ACAGCCACCACTCCA[C/G]GCTTCCCAGGGGCTT	55658
rs756246131	snp	C/T	0.000162298	0.00900682	utr-variant-3-prime	RNF126	GRCh38.p7	19:648114	CCCGTGCTTTCCCGA[C/T]GGCCGACGTGGGCTC	55658
rs756254130	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660927	GCCCTTGGGATCACC[C/T]GCGGGGTGGACACGG	55658
rs756438157	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652558	CGTGGCCCCTTCCCC[A/G]GAGGGCCTGGGTCAC	55658
rs756568943	snp	C/T	2.74903e-05	0.00370734	missense	RNF126	GRCh38.p7	19:648885	GAGCTCTCATACCTA[C/T]GTGCTCCTCAGTGAC	55658
rs756570998	snp	A/G	1.82271e-05	0.00301881	intron-variant	RNF126	GRCh38.p7	19:651875	GGAGAGGAGGGGGGC[A/G]TGACCTCGGGGGCTC	55658
rs756626010	snp	C/T	1.71428e-05	0.00292765	missense	RNF126	GRCh38.p7	19:651824	AACTGTCCGTAGCCC[C/T]GCGGCAGCGTGAACA	55658
rs756805595	snp	C/T	3.68847e-05	0.0042943	missense	RNF126	GRCh38.p7	19:648965	CCTGTGTTTTCAAAC[C/T]GATTGAGGAGCTGAA	55658
rs756918548	snp	C/T	1.87922e-05	0.00306525	intron-variant	RNF126	GRCh38.p7	19:652806	GCTCTTCCAGCCTCT[C/T]CAACAGGGGGCTGCA	55658
rs756972015	snp	C/T	1.80657e-05	0.00300542	intron-variant	RNF126	GRCh38.p7	19:652333	GCAGTGCCGGCTACC[C/T]TGTGCCCCCATGCGC	55658
rs757042113	snp	C/T	0.000433957	0.0147238	missense, intron-variant	RNF126	GRCh38.p7	19:651653	CGGCCGGTGGCCCGC[C/T]GCGTGGTGAGGCGGG	55658
rs757072643	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659975	TTACCATGTTAGCCA[A/G]GCTGGTCTCGAACTC	55658
rs757190365	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652099	CCCCAATCCCTGGCC[C/T]GGGCCCCTGGAGGGA	55658
rs757275071	in-del	-/CT			intron-variant	RNF126	GRCh38.p7	19:662661	CCACCGGGCAATACC[-/CT]CTCTCTGCTCGCCGG	55658
rs757284601	snp	A/C			downstream-variant-500B	RNF126	GRCh38.p7	19:647506	ACGCACGGGCGCAGA[A/C]GGAAAGCCACAGCAC	55658
rs757343895	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653640	TGGTGATGGCGGAGC[A/G]TGCCGAGCATTCGTG	55658
rs757407920	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:653191	GCCCCACCGTGACGG[C/G]CGTCACCAGTGCCTG	55658
rs757421857	snp	A/G	4.81696e-05	0.00490739	intron-variant	RNF126	GRCh38.p7	19:651944	ACAAAGGAGAAAGCA[A/G]GACGGGCCCTGCTGG	55658
rs757429538	snp	C/T	7.1564e-05	0.00598138	intron-variant	RNF126	GRCh38.p7	19:652199	CCCGAGCAAGGCTGA[C/T]ACGATCGGGAAGCAC	55658
rs757439440	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661499	ACCTTCGCCCCACAC[C/T]CGAGATTTCACTTTA	55658
rs757614033	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660941	CCGCGGGGTGGACAC[A/G]GGCAGGCCCCCGCAG	55658
rs757744084	snp	A/T	3.5097e-05	0.00418894	utr-variant-3-prime	RNF126	GRCh38.p7	19:648103	GTGGGAAAGGCCCCG[A/T]GCTTTCCCGACGGCC	55658
rs758051591	snp	C/G	4.26212e-05	0.00461614	missense	RNF126	GRCh38.p7	19:652249	TCCAACGGTGGCCGG[C/G]TCTGGTCTGTGGGAG	55658
rs758210377	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:652777	ACACCCCTACAACAG[C/G]TGAGGCCCGGCTGGC	55658
rs758284059	snp	C/T	0.000122624	0.00782924	intron-variant	RNF126	GRCh38.p7	19:651604	GCCACCCCCGGGGCC[C/T]CCTCACCCTTCCAGC	55658
rs758293288	snp	A/G	9.06824e-05	0.00673298	intron-variant	RNF126	GRCh38.p7	19:648291	TGCTTTGTGGGGACA[A/G]AGGCAGGGACGGGAG	55658
rs758425737	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654889	GGAGAATCGCTTGAA[C/T]CTAGGAGGCGGAGGC	55658
rs758501438	snp	A/C	1.78848e-05	0.00299033	intron-variant	RNF126	GRCh38.p7	19:649008	AGAGTGCCGGGAGCT[A/C]CTCGGGGGCCCGGCC	55658
rs758586401	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:654259	AGTGAAGAGGCACCA[C/T]CTACAATATAGAAAA	55658
rs758639799	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:663799	AATACAGGCAGACCC[A/G]GGGCTCAGGGCGCTG	55658
rs758647113	snp	A/G	0.00011281	0.00750946	intron-variant	RNF126	GRCh38.p7	19:651934	GGGCACAAAGACAAA[A/G]GAGAAAGCAAGACGG	55658
rs758764497	snp	A/G	5.00371e-05	0.00500161	utr-variant-3-prime	RNF126	GRCh38.p7	19:648096	AGGGTGGGTGGGAAA[A/G]GCCCCGTGCTTTCCC	55658
rs758776393	snp	A/G	7.23476e-05	0.00601403	utr-variant-3-prime	RNF126	GRCh38.p7	19:647905	TGAGGTTAGACAGAG[A/G]ACGGGGAGGCTGGGG	55658
rs758792625	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664925	GGATTACAGGCGTAA[A/G]CCACCGCGCCCGGCC	55658
rs758794475	in-del	-/ACTCACCAGGGACCCTGGCTGGGGATGGGGACAGGCACCCCCACCC			intron-variant	RNF126	GRCh38.p7	19:649859	CAGGCACCCCCTCCT[lengthTooLong]ACTCACCAGGGACCC	55658
rs758811304	snp	A/G	1.91254e-05	0.0030923	intron-variant	RNF126	GRCh38.p7	19:652899	CCTGCAGGAGAGAAC[A/G]GGAGGCCGGGTCACG	55658
rs758839397	snp	C/T	7.84406e-05	0.00626212	missense	RNF126	GRCh38.p7	19:649746	TTTGAGTGCAGGACT[C/T]CCCTGGAGGTGGAAG	55658
rs758861789	in-del	-/C			upstream-variant-2KB	RNF126	GRCh38.p7	19:664049	ATGCATTTCTTTTTT[-/C]TTTTTTTTTTTGAGA	55658
rs758903095	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661698	GCCCCTTCCTGGGTC[C/T]CTACTCCCGGGGAAC	55658
rs759074549	snp	A/G	1.69974e-05	0.0029152	synonymous-codon	RNF126	GRCh38.p7	19:651802	GTCATCGAAGATGCC[A/G]AAAGCAAACTGTCCG	55658
rs759108813	snp	C/T	5.16422e-05	0.00508119	synonymous-codon	RNF126	GRCh38.p7	19:648140	GGCTCACGAGTTGCT[C/T]GTGGCGTTCTCGTTG	55658
rs759136303	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652384	AAGCCTATGTTGGGA[A/G]AGCAGGAATTGTCCT	55658
rs759162819	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647496	CCTTTTCCTGACGCA[C/T]GGGCGCAGAAGGAAA	55658
rs759325305	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:654074	CTCTGGGGAGAAGCG[A/G]GGGTCTGGCGTGCAG	55658
rs759337261	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:660342	AGAGCCCAGGACAGC[A/C]AAGGAGGCCCGGAAC	55658
rs759399270	snp	A/T	2.79037e-05	0.00373512	missense	RNF126	GRCh38.p7	19:648934	CTGGATTTTCTCTTT[A/T]TCTGCCGGTGGGGGG	55658
rs759413207	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:653615	GACTCCTCATGGATG[G/T]CTGGGCCCCTGGTGA	55658
rs759422177	snp	C/T	1.76008e-05	0.0029665	splice-acceptor-variant	RNF126	GRCh38.p7	19:651856	GTGCTGGTCCACGTG[C/T]TGGGGAGAGGAGGGG	55658
rs759454383	snp	G/T	0.00245423	0.0349442	intron-variant	RNF126	GRCh38.p7	19:648841	AGGCGTGGCGGCGGG[G/T]GCCTGTAATTCCCAC	55658
rs759467675	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:655325	GAACCAGACCCTGCC[-/A]AAAAAAAAAAAGAAA	55658
rs759498678	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:662033	GGTTAAAAATGCAGA[A/C]CACCGCCGGGCACGG	55658
rs759602879	snp	A/C/T	0.000267172	0.0115553	missense, intron-variant	RNF126	GRCh38.p7	19:651638	GGGACGCCTTCGTGC[A/C/T]GGCCGGTGGCCCGCC	55658
rs759602996	snp	C/G/T	3.57106e-05	0.00422543	missense	RNF126	GRCh38.p7	19:652863	CGATAAAACCAGACT[C/G/T]GCATCTTGGACAGAT	55658
rs759685163	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:650995	TGACCTCCCAGAGAA[A/C]TGCAAATACAGCACT	55658
rs759731550	in-del	-/CCGCG			intron-variant	RNF126	GRCh38.p7	19:662636	GGCCCAGCCCCTGCC[-/CCGCG]CCGCGCCACCGGGCA	55658
rs759837442	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:655840	GCACCTCAGAGCACG[A/C]CTCAACCATGGAAAG	55658
rs759841734	snp	A/G	8.39877e-05	0.00647972	synonymous-codon	RNF126	GRCh38.p7	19:648402	CACGATGCAGCCGTC[A/G]TGGAACAGGTGGTTG	55658
rs759915453	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652664	CATCACAGAAGAGAA[C/T]GGCACGCTGCTGTCT	55658
rs760003436	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660403	GCAGGCACACAGCCC[A/G]TGGCAGCCAGTCCCC	55658
rs760019278	in-del	-/GGGGGGGGGGGGGGGGGGGGGG			intron-variant	RNF126	GRCh38.p7	19:648352	TCGGGGTGGGGGGGC[-/GGGGGGGGGGGGGGGGGGGGGG]GGGTGGGCGGGGCAC	55658
rs760032468	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:650173	GGATGGGGACAGGCA[-/C]CCCCACCCACTCACC	55658
rs760219940	in-del	-/C	1.70461e-05	0.00291938	frameshift-variant	RNF126	GRCh38.p7	19:651814	CCGAAAGCAAACTGT[-/C]CCGTAGCCCTGCGGC	55658
rs760254286	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652709	GCTCCCGGAGCCACA[A/G]ACACCAGGGCCTGAC	55658
rs760438282	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659928	GCCACCACGCCTGGC[C/T]AATCTTTTGTATTTT	55658
rs760534046	snp	A/C/G	5.1035e-05	0.00505127	missense, synonymous-codon	RNF126	GRCh38.p7	19:651793	CTCGAAGCTGTCATC[A/C/G]AAGATGCCGAAAGCA	55658
rs760553704	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647590	TTTTCCTTTAAAAAA[A/G]TCTGTTGGAGCAGTT	55658
rs760587306	snp	G/T	1.78086e-05	0.00298396	missense	RNF126	GRCh38.p7	19:651749	TCCCTGCCGTCGTCA[G/T]CCTGCGCCCCAGGAG	55658
rs760609184	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655459	CCACTGCACTCTAGC[C/T]CGGGCGACAGAGTGA	55658
rs760623987	snp	C/T	8.56091e-05	0.00654196	intron-variant	RNF126	GRCh38.p7	19:648837	AGCCAGGCGTGGCGG[C/T]GGGTGCCTGTAATTC	55658
rs760638925	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660042	AGCGATGGGACCACA[A/G]GCGTGAGCCACCGCG	55658
rs760860958	snp	A/G	2.53264e-05	0.00355845	missense	RNF126	GRCh38.p7	19:648908	TCAGTGACGGGGACG[A/G]TGGGGAGGGCCTGGA	55658
rs760902878	snp	A/G	3.43141e-05	0.00414197	intron-variant	RNF126	GRCh38.p7	19:652303	TCTGTGCTCCTGGGG[A/G]GAGAGTGCAGGTCAG	55658
rs760914725	snp	A/G	0.000116252	0.00762316	intron-variant	RNF126	GRCh38.p7	19:651588	GCGTGGGGCCCTCGC[A/G]GCCACCCCCGGGGCC	55658
rs760934536	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651431	CCCTGAACCGGCATA[C/T]TTCTGTCTCCGAAGG	55658
rs760938355	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656515	TTAGCTGGGCACGGT[A/G]GTGGGTGCCTGTAAT	55658
rs760946670	snp	A/G	5.97604e-05	0.00546595	intron-variant	RNF126	GRCh38.p7	19:648330	GGTTAGAGGCGGGAG[A/G]GCCGCGGTCGGGGTG	55658
rs760978545	in-del	-/AAAAAAAAAAAAA			intron-variant	RNF126	GRCh38.p7	19:654656	CTCAAAAAAAAAAAA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAGTG	55658
rs761154921	snp	A/G	0.000128499	0.00801455	missense	RNF126	GRCh38.p7	19:648243	GCCGTGTTCTGTCCC[A/G]TGAGGCTTTTTCGGC	55658
rs761308830	snp	A/T	5.80063e-05	0.00538515	utr-variant-3-prime	RNF126	GRCh38.p7	19:647862	TTTAAAATTATAAAA[A/T]TCTTTCCACCGCTGA	55658
rs761428699	snp	C/T	6.38753e-05	0.00565098	intron-variant	RNF126	GRCh38.p7	19:651922	CTGGGGGCGCTAGGG[C/T]ACAAAGACAAAGGAG	55658
rs761620713	snp	A/G	2.40555e-05	0.00346802	utr-variant-3-prime	RNF126	GRCh38.p7	19:647984	CGGTGGGCCGGGCCC[A/G]GGTCCTGCCCTGGAA	55658
rs761653600	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660707	CCATCACGGCTCACC[A/G]CAGCCTCCACCTCCC	55658
rs761653943	snp	A/G	3.2293e-05	0.00401814	missense	RNF126	GRCh38.p7	19:651699	CGCCGTACCGGTGCC[A/G]GGACGGATGGTCTCT	55658
rs761723917	snp	C/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664402	ACTGCACACCAGACC[C/G]TATGCTGAATGCACG	55658
rs761817820	snp	C/T	8.15096e-05	0.00638343	intron-variant	RNF126	GRCh38.p7	19:648497	CGGAGCCTGCGGGAG[C/T]GTGCAGCTGCGGTCA	55658
rs761858238	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656190	GGTGTGTGAAAATAC[C/T]GAGATAAAGCTATTA	55658
rs761952007	snp	A/G	8.55469e-05	0.00653958	intron-variant	RNF126	GRCh38.p7	19:648833	TATGAGCCAGGCGTG[A/G]CGGCGGGTGCCTGTA	55658
rs762006563	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658231	GATGGCCTCATCCCC[A/G]GGTGGGACCTGGCAG	55658
rs762035019	snp	C/G	1.70159e-05	0.00291679	missense	RNF126	GRCh38.p7	19:651787	GGGGATCTCGAAGCT[C/G]TCATCGAAGATGCCG	55658
rs762054434	snp	G/T	3.40785e-05	0.00412772	intron-variant	RNF126	GRCh38.p7	19:652229	CGAGGGGCGGGCGAC[G/T]CACCTCCAACGGTGG	55658
rs762075303	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651508	TCTCCAGAGAGCCTA[C/T]GGATGATGCCACGTT	55658
rs762158714	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:658213	CATGCACCCCTGCAG[C/T]GTGATGGCCTCATCC	55658
rs762398345	in-del	-/CT			intron-variant	RNF126	GRCh38.p7	19:661575	GAGGAAACCACACCT[-/CT]CTCTTTCCACTCCTG	55658
rs762402257	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653831	AAAATGGCCTCACAC[A/G]GCACGTGTCATCACG	55658
rs762445388	snp	A/G	6.22394e-05	0.00557816	missense	RNF126	GRCh38.p7	19:648947	TTATCTGCCGGTGGG[A/G]GGCCTGTGTTTTCAA	55658
rs762501438	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653071	CCTCTGCCAGCCACC[C/T]GCTGACCCTTTGGTG	55658
rs762529889	snp	A/C			downstream-variant-500B	RNF126	GRCh38.p7	19:647481	AGCCTCCCAGCTTGG[A/C]CTTTTCCTGACGCAC	55658
rs762709211	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:662517	CTGCCTCCAAGGCGG[C/G]GGCCAGGGCTCCACG	55658
rs762721857	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:661882	GCTCCCCTCAAGCTG[G/T]CCAAGCGGCTCCCGA	55658
rs762748505	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:657452	CCCTGGCCTCCTCTT[-/G]GCCCCCGCTGTCCTG	55658
rs762757415	snp	A/C	1.79069e-05	0.00299218	missense	RNF126	GRCh38.p7	19:652865	ATAAAACCAGACTCG[A/C]ATCTTGGACAGATAT	55658
rs762797606	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653096	TTGGTGGCTCCCGGC[A/G]ATCTGAGCCCCTCCG	55658
rs762809789	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:661168	GGTCCTCCGTGTCCA[A/C]GGCCACGGGGCGAGG	55658
rs762825104	snp	C/T	1.73327e-05	0.00294381	intron-variant	RNF126	GRCh38.p7	19:649671	TCTGGGCCGTGGCCA[C/T]GCTGTACCTGTGTGA	55658
rs762909510	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651536	GTTTCCGTGGAACCC[A/G]TGCTGGATTCTAAGC	55658
rs762937715	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655480	GACAGAGTGACACTC[C/T]ATCTCAAAAAAAAAG	55658
rs762957749	snp	A/T	1.94653e-05	0.00311966	intron-variant	RNF126	GRCh38.p7	19:652789	CAGCTGAGGCCCGGC[A/T]GGCTCTTCCAGCCTC	55658
rs763016441	snp	C/T	6.269e-05	0.00559831	missense	RNF126	GRCh38.p7	19:648415	TCGTGGAACAGGTGG[C/T]TGCAGGGCAGCTGCC	55658
rs763084279	snp	C/T	1.86932e-05	0.00305716	missense	RNF126	GRCh38.p7	19:651740	CTCTCAGGGTCCCTG[C/T]CGTCGTCAGCCTGCG	55658
rs763100693	snp	A/G	5.19036e-05	0.00509402	intron-variant	RNF126	GRCh38.p7	19:648492	GAGCCCGGAGCCTGC[A/G]GGAGTGTGCAGCTGC	55658
rs763400029	snp	G/T	7.37599e-05	0.00607244	intron-variant	RNF126	GRCh38.p7	19:651945	CAAAGGAGAAAGCAA[G/T]ACGGGCCCTGCTGGG	55658
rs763454778	snp	A/G	3.52299e-05	0.00419687	intron-variant	RNF126	GRCh38.p7	19:652197	GCCCCGAGCAAGGCT[A/G]ACACGATCGGGAAGC	55658
rs763571621	in-del	-/CCCTGGCTGGGGATGGGGACAGGCACCCCCACCCACTCACCAGGGG	8.3868e-05	0.0064751	intron-variant	RNF126	GRCh38.p7	19:650193	CCCACTCACCAGGGA[lengthTooLong]CCCAGGCTGGGGATG	55658
rs763588146	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656302	CTGCAGTGAGCCAAG[A/G]TTGCAGCAACAGAGT	55658
rs763711395	snp	C/T	1.72163e-05	0.00293391	intron-variant	RNF126	GRCh38.p7	19:649674	GGGCCGTGGCCACGC[C/T]GTACCTGTGTGATGA	55658
rs763724934	snp	C/T	3.30028e-05	0.00406205	intron-variant	RNF126	GRCh38.p7	19:652793	TGAGGCCCGGCTGGC[C/T]CTTCCAGCCTCTTCA	55658
rs763741148	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664295	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	55658
rs763752845	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652724	GACACCAGGGCCTGA[C/T]GGCCCCACACTCGGC	55658
rs763834894	snp	C/T	3.32563e-05	0.00407763	missense	RNF126	GRCh38.p7	19:648954	CCGGTGGGGGGCCTG[C/T]GTTTTCAAACTGATT	55658
rs763839445	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652504	AAACCGGTGCAGACC[C/T]CAACAGCCTCCTAAG	55658
rs763929075	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659937	CCTGGCCAATCTTTT[A/G]TATTTTTAGTAGGGA	55658
rs764057349	snp	A/G	7.32628e-05	0.00605194	missense	RNF126	GRCh38.p7	19:651693	GTCGGGCGCCGTACC[A/G]GTGCCGGGACGGATG	55658
rs764118144	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661429	AGCTGGAAGAGGCAA[A/G]AGCGAGACCCCTGGG	55658
rs764181361	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:662052	CGCCGGGCACGGTGG[C/T]TCACACCTGTAATCC	55658
rs764215057	snp	G/T	1.67925e-05	0.00289758	missense	RNF126	GRCh38.p7	19:648416	CGTGGAACAGGTGGT[G/T]GCAGGGCAGCTGCCG	55658
rs764232720	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651450	TGTCTCCGAAGGGCC[A/G]TGTGGGGAGTCACAG	55658
rs764322460	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:657476	TGTCCTGCCCGCAGC[A/G]GCCGTGGGGCCTGGT	55658
rs764403569	snp	A/G/T	7.17283e-05	0.00598824	intron-variant	RNF126	GRCh38.p7	19:652198	CCCCGAGCAAGGCTG[A/G/T]CACGATCGGGAAGCA	55658
rs764491256	snp	A/G	9.19033e-05	0.00677814	intron-variant	RNF126	GRCh38.p7	19:652226	GCACGAGGGGCGGGC[A/G]ACTCACCTCCAACGG	55658
rs764493560	snp	A/G	0.000110096	0.00741861	missense	RNF126	GRCh38.p7	19:650250	AGGGGCCCAGGCTGG[A/G]GATGGTGGCGGGCGT	55658
rs764571657	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:656562	CTGAGGCACGAGAAT[A/C]GCTTAAACCCGGCAG	55658
rs764693117	snp	C/T	3.63194e-05	0.00426126	utr-variant-3-prime	RNF126	GRCh38.p7	19:648098	GGTGGGTGGGAAAGG[C/T]CCCGTGCTTTCCCGA	55658
rs764728487	snp	A/G	6.18754e-05	0.00556182	intron-variant	RNF126	GRCh38.p7	19:650314	GGAAAAGAGAGCGCC[A/G]GTCACGGGGTGAGGC	55658
rs764763421	snp	A/G	1.77303e-05	0.00297739	intron-variant	RNF126	GRCh38.p7	19:651862	GTCCACGTGCTGGGG[A/G]GAGGAGGGGGGCGTG	55658
rs764866241	snp	G/T	3.22253e-05	0.00401393	missense	RNF126	GRCh38.p7	19:648217	CCCCAGTGAGGCCAG[G/T]GGGGTTCGTGGCCGT	55658
rs764911214	snp	C/G	1.70845e-05	0.00292267	intron-variant	RNF126	GRCh38.p7	19:648843	GCGTGGCGGCGGGTG[C/G]CTGTAATTCCCACTA	55658
rs764954212	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653072	CTCTGCCAGCCACCC[A/G]CTGACCCTTTGGTGG	55658
rs764968399	snp	C/T	1.70067e-05	0.002916	missense	RNF126	GRCh38.p7	19:651807	CGAAGATGCCGAAAG[C/T]AAACTGTCCGTAGCC	55658
rs764988841	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660827	TTCTGTAGAGACAGG[A/G]TCCTGCCACGTACGG	55658
rs765140363	snp	A/G	1.76219e-05	0.00296827	intron-variant	RNF126	GRCh38.p7	19:652318	AGAGAGTGCAGGTCA[A/G]CAGTGCCGGCTACCC	55658
rs765156086	snp	C/G/T	6.15366e-05	0.00554658	intron-variant	RNF126	GRCh38.p7	19:651602	CGGCCACCCCCGGGG[C/G/T]CCCCTCACCCTTCCA	55658
rs765318410	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:654241	AACCCACCGTGAGGG[G/T]AGAGTGAAGAGGCAC	55658
rs765373103	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:652802	GCTGGCTCTTCCAGC[C/T]TCTTCAACAGGGGGC	55658
rs765471609	snp	A/G	0.000281696	0.0118646	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651688	GGGCTGTCGGGCGCC[A/G]TACCGGTGCCGGGAC	55658
rs765574310	snp	A/G	2.1985e-05	0.00331542	intron-variant	RNF126	GRCh38.p7	19:651928	GCGCTAGGGCACAAA[A/G]ACAAAGGAGAAAGCA	55658
rs765735123	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:657684	GTGCCATCGAGGACG[A/C]CAAGGGCTGCGACCC	55658
rs765863876	snp	A/G	3.81366e-05	0.00436656	utr-variant-3-prime	RNF126	GRCh38.p7	19:648083	GTGGCGCTGGCTGAG[A/G]GTGGGTGGGAAAGGC	55658
rs766060231	snp	A/T	2.68402e-05	0.00366325	missense	RNF126	GRCh38.p7	19:648133	CGACGTGGGCTCACG[A/T]GTTGCTTGTGGCGTT	55658
rs766092826	in-del	-/G	5.36601e-05	0.00517949	intron-variant	RNF126	GRCh38.p7	19:651867	GTGCTGGGGAGAGGA[-/G]GGGGGGCGTGACCTC	55658
rs766105222	snp	A/C	0.0123511	0.0776079	intron-variant	RNF126	GRCh38.p7	19:663001	CGGCCTTGCCTCAGG[A/C]CTGCGGCGCAGACCC	55658
rs766124679	snp	C/T	1.77599e-05	0.00297987	missense	RNF126	GRCh38.p7	19:651750	CCCTGCCGTCGTCAG[C/T]CTGCGCCCCAGGAGG	55658
rs766150925	in-del	-/TTGG			upstream-variant-2KB	RNF126	GRCh38.p7	19:664551	AGGGATGAATAGGAT[-/TTGG]TTGGAGTTGGACTTC	55658
rs766160078	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653518	TGTGCCGAGCAGGAC[A/G]GATGCCATCCCCTGT	55658
rs766223411	snp	A/G	0.000220483	0.0104973	intron-variant	RNF126	GRCh38.p7	19:648508	GGAGTGTGCAGCTGC[A/G]GTCACAGCGGGCGTG	55658
rs766292108	snp	A/G	1.69899e-05	0.00291456	missense	RNF126	GRCh38.p7	19:652240	CGACTCACCTCCAAC[A/G]GTGGCCGGCTCTGGT	55658
rs766379862	snp	A/T	0.000834768	0.0204129	intron-variant	RNF126	GRCh38.p7	19:652307	TGCTCCTGGGGAGAG[A/T]GTGCAGGTCAGCAGT	55658
rs766462956	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652219	TCGGGAAGCACGAGG[A/G]GCGGGCGACTCACCT	55658
rs766481340	snp	C/G	1.67419e-05	0.00289321	missense	RNF126	GRCh38.p7	19:648249	TTCTGTCCCGTGAGG[C/G]TTTTTCGGCAGACGG	55658
rs766487111	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658352	ACCTACAGGCCCCAG[A/G]TGACTGACAGTGACC	55658
rs766536201	snp	C/T	5.79761e-05	0.00538374	intron-variant	RNF126	GRCh38.p7	19:651591	TGGGGCCCTCGCGGC[C/T]ACCCCCGGGGCCCCC	55658
rs766592162	snp	C/G/T	0.000134122	0.0081882	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651637	GGGGACGCCTTCGTG[C/G/T]CGGCCGGTGGCCCGC	55658
rs766623147	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655517	GGGGGGGGAAAGGAC[A/G]TGTACAGGACATGCC	55658
rs766653382	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:660116	GTGCCGTCGTCGCCT[A/G]AGCCCCCGACCGCAA	55658
rs766787404	snp	C/G/T	7.24087e-05	0.00601657	intron-variant	RNF126	GRCh38.p7	19:652338	GCCGGCTACCCTGTG[C/G/T]CCCCATGCGCCAGGC	55658
rs766793901	snp	C/G/T	0.000151145	0.00869206	intron-variant	RNF126	GRCh38.p7	19:651924	GGGGGCGCTAGGGCA[C/G/T]AAAGACAAAGGAGAA	55658
rs766826834	snp	C/T	0.000360685	0.0134243	intron-variant	RNF126	GRCh38.p7	19:648333	TAGAGGCGGGAGGGC[C/T]GCGGTCGGGGTGGGG	55658
rs766870770	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662714	AAACCAGGCTCACCG[A/G]GCTTAGGGATCCCAC	55658
rs766874566	in-del	-/GGGGACA	7.39016e-05	0.00607827	intron-variant	RNF126	GRCh38.p7	19:650207	ACCCAGGCTGGGGAT[-/GGGGACA]GGGGACAGGCACCCC	55658
rs766929531	snp	C/T	1.83242e-05	0.00302684	intron-variant	RNF126	GRCh38.p7	19:651879	AGGAGGGGGGCGTGA[C/T]CTCGGGGGCTCAGGC	55658
rs767080626	in-del	-/A	0.000464792	0.0152375	utr-variant-3-prime	RNF126	GRCh38.p7	19:647896	TTAGAGGGTGAGGTT[-/A]AGACAGAGGACGGGG	55658
rs767136984	snp	A/C	3.8449e-05	0.0043844	utr-variant-3-prime	RNF126	GRCh38.p7	19:648078	GCCGTGTGGCGCTGG[A/C]TGAGGGTGGGTGGGA	55658
rs767188250	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:659590	CCCTCAGCAGCTCTC[A/G]CCCACACCCTACAGT	55658
rs767192012	snp	C/T	1.8084e-05	0.00300694	intron-variant	RNF126	GRCh38.p7	19:650200	CACCAGGGACCCAGG[C/T]TGGGGATGGGGACAG	55658
rs767192139	snp	C/T	0.000351432	0.0132511	utr-variant-3-prime	RNF126	GRCh38.p7	19:647872	TAAAAATCTTTCCAC[C/T]GCTGAACGTTTAGAG	55658
rs767271630	snp	A/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647511	CGGGCGCAGAAGGAA[A/G]GCCACAGCACCGGCT	55658
rs767274152	snp	A/T	0.000183217	0.00956949	missense	RNF126	GRCh38.p7	19:652882	TCTTGGACAGATATA[A/T]TCCTGCAGGAGAGAA	55658
rs767355753	snp	A/G	2.287e-05	0.00338149	intron-variant	RNF126	GRCh38.p7	19:652933	ACGCCGGCATCACCT[A/G]CAAACCCCCCCAAGT	55658
rs767460918	snp	A/G	8.50087e-05	0.00651898	intron-variant	RNF126	GRCh38.p7	19:648498	GGAGCCTGCGGGAGT[A/G]TGCAGCTGCGGTCAC	55658
rs767466837	snp	G/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664453	AGATTGGACAGGAGC[G/T]TGGAACTCAAGGGTG	55658
rs767523043	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:653469	GTCCCAAAACCACGT[G/T]CACAGTTCCCCAGCA	55658
rs767535569	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:660877	TGCTGTCTACGGGCG[C/G]CTTGTTGCGTCCTGC	55658
rs767586943	snp	A/G	0.00012665	0.00795669	synonymous-codon	RNF126	GRCh38.p7	19:651745	AGGGTCCCTGCCGTC[A/G]TCAGCCTGCGCCCCA	55658
rs767655458	snp	A/C	1.70316e-05	0.00291813	splice-donor-variant	RNF126	GRCh38.p7	19:652231	AGGGGCGGGCGACTC[A/C]CCTCCAACGGTGGCC	55658
rs767767019	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651019	CAGCACTGAGCCACC[A/G]TGCCTGGCAAAATTA	55658
rs767884012	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656797	GTGTGTTTGGGGTGT[C/T]GGGATTGGGACGCCC	55658
rs768003782	snp	C/T	5.13545e-05	0.00506701	missense	RNF126	GRCh38.p7	19:651822	CAAACTGTCCGTAGC[C/T]CTGCGGCAGCGTGAA	55658
rs768049524	snp	A/G	2.45348e-05	0.0035024	synonymous-codon	RNF126	GRCh38.p7	19:648152	GCTTGTGGCGTTCTC[A/G]TTGCTGGGCGAGCTG	55658
rs768084832	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652670	AGAAGAGAACGGCAC[A/G]CTGCTGTCTGCACAG	55658
rs768139313	snp	C/T	0.000110695	0.00743877	synonymous-codon	RNF126	GRCh38.p7	19:648230	AGGGGGGTTCGTGGC[C/T]GTGTTCTGTCCCGTG	55658
rs768164173	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653955	AGGGGAGCCAAGGTC[A/G]ACCCCAGGCTCTGGG	55658
rs768273774	snp	C/G	2.80446e-05	0.00374453	intron-variant	RNF126	GRCh38.p7	19:651959	AGACGGGCCCTGCTG[C/G]GTGCCGGGTGGGAGG	55658
rs768326864	snp	A/G	2.05518e-05	0.00320554	intron-variant	RNF126	GRCh38.p7	19:651915	CAGTCTGCTGGGGGC[A/G]CTAGGGCACAAAGAC	55658
rs768351957	snp	G/T	0.00145285	0.0269131	missense	RNF126	GRCh38.p7	19:648376	GGGGCACTCACCTGC[G/T]CCAGCCAGGGCACGA	55658
rs768416894	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:650889	GAGCCACCTCACCCA[A/G]CCTCAGCTACTTTTT	55658
rs768588820	snp	A/C	5.52074e-05	0.00525363	synonymous-codon	RNF126	GRCh38.p7	19:650296	GAGCTGCTGGATGAT[A/C]CTGGAAAAGAGAGCG	55658
rs768843086	snp	A/G	0.000257208	0.0113375	missense	RNF126	GRCh38.p7	19:651827	TGTCCGTAGCCCTGC[A/G]GCAGCGTGAACAGGT	55658
rs768933054	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:658136	CACCCGGCATCATCA[C/T]CATAGCAACAGCTGG	55658
rs768972107	snp	C/T	0.000178834	0.00945436	missense	RNF126	GRCh38.p7	19:648900	CGTGCTCCTCAGTGA[C/T]GGGGACGGTGGGGAG	55658
rs769049673	snp	A/G			downstream-variant-500B	RNF126	GRCh38.p7	19:647395	GCAGTTTTGCTAGCC[A/G]GCCCTGGGTGCCAAG	55658
rs769146743	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661163	GTCAAGGTCCTCCGT[A/G]TCCAAGGCCACGGGG	55658
rs769259105	snp	A/G	0.000165641	0.00909906	intron-variant	RNF126	GRCh38.p7	19:651575	TTCCGACCTCAAGGC[A/G]TGGGGCCCTCGCGGC	55658
rs769316379	snp	A/G	4.38529e-05	0.00468236	synonymous-codon	RNF126	GRCh38.p7	19:652269	GTCTGTGGGAGCTGT[A/G]GAGGGGGCAGAACCA	55658
rs769317084	snp	A/G/T			intron-variant	RNF126	GRCh38.p7	19:653853	GTCATCACGCCAGGG[A/G/T]CTCACATGGGGGTCC	55658
rs769403131	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662676	CTCTCTCTGCTCGCC[A/G]GGCCTCAGTTTCTCC	55658
rs769494147	snp	C/T	0.000745182	0.0192882	missense, intron-variant	RNF126	GRCh38.p7	19:651627	CTTCCAGCGTGGGGA[C/T]GCCTTCGTGCCGGCC	55658
rs769528654	snp	C/G	0.00391388	0.0440638	intron-variant	RNF126	GRCh38.p7	19:648360	GGGGGGGCGGGTGGG[C/G]GGGGCACTCACCTGC	55658
rs769556400	in-del	-/CTTT			intron-variant	RNF126	GRCh38.p7	19:657320	TCTGTGCATCACTGG[-/CTTT]CTGTCGGGCTCCCGG	55658
rs769565416	snp	A/G	9.34973e-05	0.00683666	intron-variant	RNF126	GRCh38.p7	19:649791	GCTGACGGGCAGCTG[A/G]GGCAGGTGCGTCTAT	55658
rs769622641	snp	A/G	7.70208e-05	0.0062052	intron-variant	RNF126	GRCh38.p7	19:651948	AGGAGAAAGCAAGAC[A/G]GGCCCTGCTGGGTGC	55658
rs769673982	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655925	ACATCACGTCCAGTG[A/G]GAGATGCCAGACACA	55658
rs769723552	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664951	CGGCCTGCATTTAGG[A/G]TTTTGAATGTCCAGA	55658
rs769821288	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:651503	CGGCCTCTCCAGAGA[A/G]CCTATGGATGATGCC	55658
rs769930215	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652604	GGCTGAGGGAGGTGA[A/G]CGGCTGCACAGGTTG	55658
rs769978706	snp	C/G	1.89102e-05	0.00307486	missense	RNF126	GRCh38.p7	19:651737	CGGCTCTCAGGGTCC[C/G]TGCCGTCGTCAGCCT	55658
rs770017566	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:660156	CCCGCTCAGGACACC[C/G]TCACGAGTCACCAGG	55658
rs770030985	snp	C/T	0.00133244	0.0257769	utr-variant-3-prime	RNF126	GRCh38.p7	19:647968	TCCCAAGCCAGGGGG[C/T]CGGTGGGCCGGGCCC	55658
rs770112242	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:659075	GCAGGGAGCCCGTTC[C/T]GGAGAACCCAGCTGT	55658
rs770206476	snp	A/G	1.71699e-05	0.00292996	missense	RNF126	GRCh38.p7	19:651770	GCCCCAGGAGGGAAC[A/G]TGGGGATCTCGAAGC	55658
rs770249674	in-del	-/AAAG			intron-variant	RNF126	GRCh38.p7	19:654998	CTTACAACTCAAAAG[-/AAAG]AAAGAAAGAAAGAAA	55658
rs770314205	in-del	-/TGGGC	0.000182332	0.00954635	intron-variant	RNF126	GRCh38.p7	19:648356	GGGTGGGGGGGCGGG[-/TGGGC]GGGGCACTCACCTGC	55658
rs770441770	snp	A/G/T	0.000136828	0.00827029	missense	RNF126	GRCh38.p7	19:648201	GAGGAGGAGAAGCTC[A/G/T]CCCCAGTGAGGCCAG	55658
rs770505436	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:653984	GGGATGCAGGTTGCA[C/T]CGGGGCTGTTCAGTC	55658
rs770534456	snp	A/C	5.94301e-05	0.00545083	intron-variant	RNF126	GRCh38.p7	19:650308	GATCCTGGAAAAGAG[A/C]GCGCCAGTCACGGGG	55658
rs770620677	snp	A/G	4.31751e-05	0.00464604	synonymous-codon	RNF126	GRCh38.p7	19:652260	CCGGCTCTGGTCTGT[A/G]GGAGCTGTGGAGGGG	55658
rs770798112	snp	A/G	0.00020202	0.0100483	intron-variant	RNF126	GRCh38.p7	19:648302	GACAGAGGCAGGGAC[A/G]GGAGAAGGGGCAGGT	55658
rs770854936	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662090	TTGGGAGGCTGAGCC[A/G]GAAGAATCGCTTGAG	55658
rs770972244	snp	C/T	2.53701e-05	0.00356152	missense	RNF126	GRCh38.p7	19:648909	CAGTGACGGGGACGG[C/T]GGGGAGGGCCTGGAT	55658
rs771017508	snp	C/T	3.49192e-05	0.00417833	synonymous-codon	RNF126	GRCh38.p7	19:651757	GTCGTCAGCCTGCGC[C/T]CCAGGAGGGAACGTG	55658
rs771095213	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:656223	ATAAATGGGCCAGGC[A/G]CCTGTGGTCCCAGCT	55658
rs771113847	snp	A/G	1.77912e-05	0.0029825	missense	RNF126	GRCh38.p7	19:652842	TGGTCTCTTCCGGAA[A/G]CTCCTCGATAAAACC	55658
rs771155426	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650450	TGAGCCAGGGTCTCA[C/T]TCTAATGCCGAGGCA	55658
rs771165185	snp	A/C	3.91926e-05	0.0044266	intron-variant	RNF126	GRCh38.p7	19:652775	CCACACCCCTACAAC[A/C]GCTGAGGCCCGGCTG	55658
rs771222790	in-del	-/CTG			downstream-variant-500B	RNF126	GRCh38.p7	19:647337	AGTGACACTGCCACC[-/CTG]CTACCTCGCCAGCAG	55658
rs771238022	snp	A/G	0.00538665	0.0516169	utr-variant-3-prime	RNF126	GRCh38.p7	19:647913	GACAGAGGACGGGGA[A/G]GCTGGGGACGCCCCA	55658
rs771239827	in-del	-/TC	0.000430459	0.0146644	intron-variant	RNF126	GRCh38.p7	19:648349	CGGTCGGGGTGGGGG[-/TC]GGCGGGTGGGCGGGG	55658
rs771259571	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:660323	GGGGCCTCAGCCTGA[A/T]CCCAGAGCCCAGGAC	55658
rs771421574	snp	A/G	0.000116131	0.00761917	synonymous-codon	RNF126	GRCh38.p7	19:648468	GTCGTCCTTGCACAC[A/G]GGGCACTCGAGCCCG	55658
rs771657856	snp	A/G	4.61457e-05	0.0048032	intron-variant	RNF126	GRCh38.p7	19:652220	CGGGAAGCACGAGGG[A/G]CGGGCGACTCACCTC	55658
rs771671549	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660626	CAGGTGTGCCCATTT[C/T]CCAGCATAAAAAATT	55658
rs771923167	snp	A/C/T	0.000492314	0.015683	synonymous-codon	RNF126	GRCh38.p7	19:648131	GCCGACGTGGGCTCA[A/C/T]GAGTTGCTTGTGGCG	55658
rs771965043	snp	C/T			upstream-variant-2KB	RNF126	GRCh38.p7	19:664766	CCTGCCTCAGGCTCC[C/T]GAGTTGCTGGGATTA	55658
rs772080826	in-del	-/G/GGGGGGGGGGGGGG	0.423311	0.180176	intron-variant	RNF126	GRCh38.p7	19:648344	GGCCGCGGTCGGGGT[-/G/GGGGGGGGGGGGGG]GGGGGGGCGGGTGGG	55658
rs772214391	in-del	-/CT			downstream-variant-500B	RNF126	GRCh38.p7	19:647115	CACTGCCCCGGCCCC[-/CT]CTGAGCCCGCAGGTC	55658
rs772267386	snp	A/C	1.84725e-05	0.00303906	intron-variant	RNF126	GRCh38.p7	19:652343	CTACCCTGTGCCCCC[A/C]TGCGCCAGGCGCTCC	55658
rs772335838	snp	A/G	1.72196e-05	0.00293419	missense	RNF126	GRCh38.p7	19:651833	TAGCCCTGCGGCAGC[A/G]TGAACAGGTGCTGGT	55658
rs772488976	snp	C/T	0.000136147	0.00824954	missense, intron-variant	RNF126	GRCh38.p7	19:651633	GCGTGGGGACGCCTT[C/T]GTGCCGGCCGGTGGC	55658
rs772552371	snp	A/G	7.51625e-05	0.0061299	intron-variant	RNF126	GRCh38.p7	19:650203	CAGGGACCCAGGCTG[A/G]GGATGGGGACAGGCA	55658
rs772610628	snp	A/G	1.73306e-05	0.00294363	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651670	CGTGGTGAGGCGGGC[A/G]CGGGGCTGTCGGGCG	55658
rs772667808	snp	C/T	1.79696e-05	0.00299741	missense	RNF126	GRCh38.p7	19:652832	CTGCATTACCTGGTC[C/T]CTTCCGGAAGCTCCT	55658
rs772724445	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661007	CAACGTCCATGATTA[A/G]ATATTTGTCAATCAC	55658
rs772904692	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661161	AGGTCAAGGTCCTCC[A/G]TGTCCAAGGCCACGG	55658
rs772925012	snp	A/G	2.6677e-05	0.00365209	missense	RNF126	GRCh38.p7	19:648196	ACGACGAGGAGGAGA[A/G]GCTCACCCCAGTGAG	55658
rs772983793	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:661869	ACCTCCTGCGGCTGC[G/T]CCCCTCAAGCTGGCC	55658
rs773274708	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:655469	CTAGCCCGGGCGACA[C/G]AGTGACACTCCATCT	55658
rs773365857	snp	C/G	4.73205e-05	0.00486395	missense	RNF126	GRCh38.p7	19:652291	GCAGAACCATTTTCT[C/G]TGCTCCTGGGGAGAG	55658
rs773443079	snp	C/G	1.72273e-05	0.00293485	missense	RNF126	GRCh38.p7	19:651835	GCCCTGCGGCAGCGT[C/G]AACAGGTGCTGGTCC	55658
rs773578713	snp	A/G/T	0.000205233	0.0101279	missense, synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651634	CGTGGGGACGCCTTC[A/G/T]TGCCGGCCGGTGGCC	55658
rs773597839	snp	C/G/T			intron-variant	RNF126	GRCh38.p7	19:659115	CTCCAGGGTGCTGGC[C/G/T]GGACGCTTGAGAGGC	55658
rs773633393	snp	C/T	0.000173646	0.00931628	missense, intron-variant	RNF126	GRCh38.p7	19:651671	GTGGTGAGGCGGGCG[C/T]GGGGCTGTCGGGCGC	55658
rs773800347	snp	A/G	0.000146307	0.00855174	intron-variant	RNF126	GRCh38.p7	19:651918	TCTGCTGGGGGCGCT[A/G]GGGCACAAAGACAAA	55658
rs773845769	snp	C/T	1.69579e-05	0.00291182	missense	RNF126	GRCh38.p7	19:648398	AGGGCACGATGCAGC[C/T]GTCGTGGAACAGGTG	55658
rs773900768	snp	A/G	4.84156e-05	0.0049199	intron-variant	RNF126	GRCh38.p7	19:648329	AGGTTAGAGGCGGGA[A/G]GGCCGCGGTCGGGGT	55658
rs773981212	snp	C/T	4.88639e-05	0.00494263	utr-variant-3-prime	RNF126	GRCh38.p7	19:647983	CCGGTGGGCCGGGCC[C/T]GGGTCCTGCCCTGGA	55658
rs773983910	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:655068	TGATCCCAGTACTTT[C/G]GGAAGCCAAGGTGGG	55658
rs774043765	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647492	TTGGCCTTTTCCTGA[C/T]GCACGGGCGCAGAAG	55658
rs774147366	snp	C/T	0.000155219	0.00880826	intron-variant	RNF126	GRCh38.p7	19:650194	CCCACTCACCAGGGA[C/T]CCAGGCTGGGGATGG	55658
rs774398964	snp	C/T	3.00278e-05	0.00387466	utr-variant-3-prime	RNF126	GRCh38.p7	19:648121	TTTCCCGACGGCCGA[C/T]GTGGGCTCACGAGTT	55658
rs774423534	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:650946	ATTGCTCAGGCTGGT[C/T]TTAAACTCCTGTCCT	55658
rs774447925	snp	A/G	7.73365e-05	0.0062179	intron-variant	RNF126	GRCh38.p7	19:648494	GCCCGGAGCCTGCGG[A/G]AGTGTGCAGCTGCGG	55658
rs774497524	snp	C/G	2.12809e-05	0.0032619	intron-variant	RNF126	GRCh38.p7	19:652922	GGGTCACGGTGACGC[C/G]GGCATCACCTGCAAA	55658
rs774507945	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:657326	CATCACTGGCTTTCT[C/G]TCGGGCTCCCGGGTT	55658
rs774598664	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:649609	GTGGGTCCAGGCAGT[-/G]GGGCAGCTCCCAGGG	55658
rs774647825	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652083	CAAGCAGCGTGGGCC[A/G]CCCCAATCCCTGGCC	55658
rs774727819	snp	A/G	4.41511e-05	0.00469825	missense	RNF126	GRCh38.p7	19:652273	GTGGGAGCTGTGGAG[A/G]GGGCAGAACCATTTT	55658
rs774901524	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:660337	ATCCCAGAGCCCAGG[A/T]CAGCAAAGGAGGCCC	55658
rs774983937	snp	A/G	3.24417e-05	0.00402738	missense	RNF126	GRCh38.p7	19:648220	CAGTGAGGCCAGGGG[A/G]GTTCGTGGCCGTGTT	55658
rs774984194	snp	A/G	6.78541e-05	0.0058243	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651628	TTCCAGCGTGGGGAC[A/G]CCTTCGTGCCGGCCG	55658
rs775035092	snp	C/T	5.58581e-05	0.0052845	intron-variant	RNF126	GRCh38.p7	19:651582	CTCAAGGCGTGGGGC[C/T]CTCGCGGCCACCCCC	55658
rs775166175	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660656	TCGTTTTTGAGACAG[C/T]GTCTTGCTTGTCACC	55658
rs775272158	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664830	GTATTTTTAGTAGAC[A/G]GGGTTTCACTATGTT	55658
rs775276008	snp	A/G	1.78512e-05	0.00298752	intron-variant	RNF126	GRCh38.p7	19:651866	ACGTGCTGGGGAGAG[A/G]AGGGGGGCGTGACCT	55658
rs775277330	snp	A/G	2.02718e-05	0.00318363	intron-variant	RNF126	GRCh38.p7	19:651911	CGTGCAGTCTGCTGG[A/G]GGCGCTAGGGCACAA	55658
rs775490673	snp	C/T	0.000109361	0.00739383	utr-variant-3-prime	RNF126	GRCh38.p7	19:647969	CCCAAGCCAGGGGGC[C/T]GGTGGGCCGGGCCCG	55658
rs775666415	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:658052	AGGCCCCATTGGAGC[A/C]TCTGGCCCTAGCAGA	55658
rs775675970	snp	A/G	7.08491e-05	0.00595143	synonymous-codon	RNF126	GRCh38.p7	19:648483	AGGGCACTCGAGCCC[A/G]GAGCCTGCGGGAGTG	55658
rs775725270	snp	A/G	9.37849e-05	0.00684716	synonymous-codon	RNF126	GRCh38.p7	19:651739	GCTCTCAGGGTCCCT[A/G]CCGTCGTCAGCCTGC	55658
rs775727301	snp	A/G/T	6.9684e-05	0.0059023	missense, synonymous-codon	RNF126	GRCh38.p7	19:648410	AGCCGTCGTGGAACA[A/G/T]GTGGTTGCAGGGCAG	55658
rs775745255	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651424	CCACACACCCTGAAC[C/T]GGCATACTTCTGTCT	55658
rs775869367	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656172	TCACCAGGTGAATTA[C/T]ATGGTGTGTGAAAAT	55658
rs775963264	snp	A/G	2.66713e-05	0.0036517	synonymous-codon	RNF126	GRCh38.p7	19:648134	GACGTGGGCTCACGA[A/G]TTGCTTGTGGCGTTC	55658
rs775985001	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:657900	AGCCGCCCTCCTCCT[C/T]CAAGGGCACAGCCAA	55658
rs776048742	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:652944	ACCTGCAAACCCCCC[C/G]AAGTGTGAGGACAGA	55658
rs776096458	in-del	-/GGAACAGGTGGTTGCAGGGCAGCTGCCGC	8.12909e-05	0.00637486	frameshift-variant	RNF126	GRCh38.p7	19:648403	CGATGCAGCCGTCGT[lengthTooLong]GGAACAGGTGGTTGC	55658
rs776165298	snp	C/G	1.81128e-05	0.00300933	intron-variant	RNF126	GRCh38.p7	19:651572	AACTTCCGACCTCAA[C/G]GCGTGGGGCCCTCGC	55658
rs776175852	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:652037	GTGAGATGCCTCGGT[-/G]GGAAGTTTCGCTTTC	55658
rs776203272	snp	A/G	9.19879e-05	0.00678126	intron-variant	RNF126	GRCh38.p7	19:652224	AAGCACGAGGGGCGG[A/G]CGACTCACCTCCAAC	55658
rs776221679	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653413	CATGGTGATGTCCCA[A/G]AGGAGACGTGAGGAC	55658
rs776311641	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653000	GCTGGCCAGGCACAC[A/G]CAGGCCAGGGTGGCT	55658
rs776322492	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661119	CACTACAGGAAGGCC[C/T]TCCCCAGGCCCAGTG	55658
rs776329643	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:650919	TAAAAATTAGAGATG[C/G]GGCCTCCCTACATTG	55658
rs776418786	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:656153	TGAATATACTACAAA[C/T]GTTTCACCAGGTGAA	55658
rs776673030	snp	G/T	1.96641e-05	0.00313555	intron-variant	RNF126	GRCh38.p7	19:652778	CACCCCTACAACAGC[G/T]GAGGCCCGGCTGGCT	55658
rs776694741	snp	C/T	9.61955e-05	0.00693459	intron-variant	RNF126	GRCh38.p7	19:649640	GTGGGCAGCCCAGCC[C/T]TCCCCCAGCAGGCAC	55658
rs776839606	in-del	-/C	0.00121507	0.0246182	intron-variant	RNF126	GRCh38.p7	19:648352	GTCGGGGTGGGGGGG[-/C]GGGTGGGCGGGGCAC	55658
rs776912512	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:658187	GGACCCTGCCAGTGC[C/G]GGGCTCCACCCATGC	55658
rs776996596	snp	A/G	8.57082e-05	0.00654574	synonymous-codon, intron-variant	RNF126	GRCh38.p7	19:651685	GCGGGGCTGTCGGGC[A/G]CCGTACCGGTGCCGG	55658
rs777052236	snp	A/G	1.68855e-05	0.00290559	synonymous-codon	RNF126	GRCh38.p7	19:648471	GTCCTTGCACACAGG[A/G]CACTCGAGCCCGGAG	55658
rs777268648	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:662743	ACCTGGGATCCTCGC[A/G]GCCTCTCGGGTCGGG	55658
rs777334099	snp	C/G	4.25541e-05	0.00461251	missense	RNF126	GRCh38.p7	19:652251	CAACGGTGGCCGGCT[C/G]TGGTCTGTGGGAGCT	55658
rs777413356	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:658645	ATCCCACATTCACAC[C/T]GTCTGTCCCTGGGCC	55658
rs777465199	snp	C/T	1.80784e-05	0.00300648	intron-variant	RNF126	GRCh38.p7	19:652331	CAGCAGTGCCGGCTA[C/T]CCTGTGCCCCCATGC	55658
rs777552430	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660907	CTCCAAAGGCACAAG[C/T]AGATGCCCTTGGGAT	55658
rs777555199	snp	C/T	6.22995e-05	0.00558085	intron-variant	RNF126	GRCh38.p7	19:651608	CCCCCGGGGCCCCCT[C/T]ACCCTTCCAGCGTGG	55658
rs777656230	snp	C/G/T	0.00641147	0.056311	intron-variant	RNF126	GRCh38.p7	19:648352	GTCGGGGTGGGGGGG[C/G/T]GGGTGGGCGGGGCAC	55658
rs777699781	in-del	-/CAAGGGGCTG	0.000416753	0.0144292	intron-variant	RNF126	GRCh38.p7	19:661323	GCCTGTCCCAGGGCT[-/CAAGGGGCTG]CAAGGGGCTGCCCTG	55658
rs777755807	snp	A/G	0.0034415	0.0413389	intron-variant	RNF126	GRCh38.p7	19:651598	CTCGCGGCCACCCCC[A/G]GGGCCCCCTCACCCT	55658
rs777943233	snp	C/T	2.41882e-05	0.00347757	utr-variant-3-prime	RNF126	GRCh38.p7	19:647907	AGGTTAGACAGAGGA[C/T]GGGGAGGCTGGGGAC	55658
rs777951789	snp	C/T	3.57737e-05	0.00422913	synonymous-codon	RNF126	GRCh38.p7	19:652837	TTACCTGGTCTCTTC[C/T]GGAAGCTCCTCGATA	55658
rs777964283	snp	C/T	5.69157e-05	0.00533429	intron-variant	RNF126	GRCh38.p7	19:651895	CTCGGGGGCTCAGGC[C/T]CGTGCAGTCTGCTGG	55658
rs777987664	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:653988	TGCAGGTTGCACCGG[A/G]GCTGTTCAGTCTTCG	55658
rs778045663	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660176	GAGTCACCAGGAGAG[C/T]GGCCAGGTGCCGGCC	55658
rs778139022	snp	A/T	8.12579e-05	0.00637357	intron-variant	RNF126	GRCh38.p7	19:649759	CTCCCCTGGAGGTGG[A/T]AGGTGGGGTTCAAGT	55658
rs778192116	snp	C/T	0.000103912	0.00720731	intron-variant	RNF126	GRCh38.p7	19:649011	GTGCCGGGAGCTCCT[C/T]GGGGGCCCGGCCCGG	55658
rs778194051	snp	A/G	2.29914e-05	0.00339045	intron-variant	RNF126	GRCh38.p7	19:651937	CACAAAGACAAAGGA[A/G]AAAGCAAGACGGGCC	55658
rs778343104	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647880	TTTCCACCGCTGAAC[A/G]TTTAGAGGGTGAGGT	55658
rs778420599	snp	A/G	5.18497e-05	0.00509138	synonymous-codon	RNF126	GRCh38.p7	19:648450	ACGCTCACCCAGCGC[A/G]TAGTCGTCCTTGCAC	55658
rs778431760	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655821	ACAGCTCCAGTGTCC[A/G]CCCGCACCTCAGAGC	55658
rs778577926	in-del	-/T			intron-variant	RNF126	GRCh38.p7	19:650584	ACCACTCTCGGCTAC[-/T]TTTTTTTTTTTTTTT	55658
rs778609543	snp	A/G			upstream-variant-2KB	RNF126	GRCh38.p7	19:664623	TAAGAGTTGGAGCCT[A/G]TGCATTTAGATTTTT	55658
rs778642525	snp	A/G	0.000112663	0.0075046	intron-variant	RNF126	GRCh38.p7	19:650300	TGCTGGATGATCCTG[A/G]AAAAGAGAGCGCCAG	55658
rs778693470	in-del	-/GC	1.9589e-05	0.00312956	intron-variant	RNF126	GRCh38.p7	19:652787	AACAGCTGAGGCCCG[-/GC]TGGCTCTTCCAGCCT	55658
rs778693521	snp	A/T	3.47965e-05	0.00417098	intron-variant	RNF126	GRCh38.p7	19:652209	GCTGACACGATCGGG[A/T]AGCACGAGGGGCGGG	55658
rs778712595	snp	A/G	2.46746e-05	0.00351236			GRCh38.p7	19:648183	GAGGAGGACGATGAC[A/G]ACGAGGAGGAGAAGC	55658
rs778779177	in-del	-/T	0.00528666	0.0511408	intron-variant	RNF126	GRCh38.p7	19:648344	GGGCCGCGGTCGGGG[-/T]GGGGGGGCGGGTGGG	55658
rs778908258	snp	A/G	0.000309717	0.0124404	synonymous-codon	RNF126	GRCh38.p7	19:648275	GACGGGGCAGCTGTC[A/G]TGCTTTGTGGGGACA	55658
rs778920611	snp	C/T			downstream-variant-500B	RNF126	GRCh38.p7	19:647123	CCGGCCCCCTGAGCC[C/T]GCAGGTCCCCACGCC	55658
rs778928943	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652665	ATCACAGAAGAGAAC[A/G]GCACGCTGCTGTCTG	55658
rs778990289	snp	A/C	1.88557e-05	0.00307042	intron-variant	RNF126	GRCh38.p7	19:651890	GTGACCTCGGGGGCT[A/C]AGGCCCGTGCAGTCT	55658
rs779002772	in-del	-/AAAAA			intron-variant	RNF126	GRCh38.p7	19:655486	GTGACACTCCATCTC[-/AAAAA]AAAAGAAAAGTGGGG	55658
rs779047012	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:651871	CTGGGGAGAGGAGGG[C/G]GGCGTGACCTCGGGG	55658
rs779084290	snp	C/T	6.99178e-05	0.00591219	intron-variant	RNF126	GRCh38.p7	19:649000	AAGAGGCGAGAGTGC[C/T]GGGAGCTCCTCGGGG	55658
rs779092394	snp	C/T	1.95406e-05	0.00312569	intron-variant	RNF126	GRCh38.p7	19:652906	GAGAGAACAGGAGGC[C/T]GGGTCACGGTGACGC	55658
rs779237195	snp	C/G	0.000395355	0.0140542	missense	RNF126	GRCh38.p7	19:651831	CGTAGCCCTGCGGCA[C/G]CGTGAACAGGTGCTG	55658
rs779275872	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:661536	CCTCCTGCTGGGGAG[A/G]GGAAGCCCTGTGGCT	55658
rs779289241	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:651123	CCTGCGACGGCTCCC[C/T]CAGGCTCTGTTCCAC	55658
rs779362582	snp	A/G	0.00307084	0.0390639	utr-variant-3-prime	RNF126	GRCh38.p7	19:647893	ACGTTTAGAGGGTGA[A/G]GTTAGACAGAGGACG	55658
rs779477114	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:661586	ACCTCTCTCTTTCCA[C/T]TCCTGGGCCTGGCCC	55658
rs779646826	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:649570	AGGCTGTGCCCGCAT[A/C]CCCTTTGACCTTTGT	55658
rs779711505	in-del	-/AGA	2.57593e-05	0.00358873	cds-indel	RNF126	GRCh38.p7	19:648193	ATGACGACGAGGAGG[-/AGA]AGCTCACCCCAGTGA	55658
rs779783705	snp	C/T	2.58055e-05	0.00359194	intron-variant	RNF126	GRCh38.p7	19:651951	AGAAAGCAAGACGGG[C/T]CCTGCTGGGTGCCGG	55658
rs779848550	snp	A/G	0.000106474	0.00729558	synonymous-codon	RNF126	GRCh38.p7	19:650281	GATGATGCCGTTGAC[A/G]AGCTGCTGGATGATC	55658
rs779853295	snp	C/T	5.15159e-05	0.00507497	synonymous-codon	RNF126	GRCh38.p7	19:648447	CACACGCTCACCCAG[C/T]GCGTAGTCGTCCTTG	55658
rs779878961	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:655544	TGCCTCCAAAAACAC[A/G]CTGGGTAAACGCAGC	55658
rs779904713	snp	A/G	0.000166293	0.00911694	intron-variant	RNF126	GRCh38.p7	19:648361	GGGGGGCGGGTGGGC[A/G]GGGCACTCACCTGCT	55658
rs779936283	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:658828	CCACCACTAGGGACT[A/G]GAACCCCACAGGTGC	55658
rs779936286	snp	A/G	0.000128008	0.00799923	utr-variant-3-prime	RNF126	GRCh38.p7	19:648115	CCGTGCTTTCCCGAC[A/G]GCCGACGTGGGCTCA	55658
rs779966267	snp	G/T			intron-variant	RNF126	GRCh38.p7	19:657165	GAAGGGCCTGAGGGA[G/T]AAGCTGTCTCCCTCT	55658
rs780054790	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647674	GTCGTGGAGGCGGCC[A/G]AGGGGGAGGCTGGGG	55658
rs780116869	snp	A/G	7.33918e-05	0.00605727	intron-variant	RNF126	GRCh38.p7	19:650331	TCACGGGGTGAGGCC[A/G]CCCCACGCACAGGAG	55658
rs780309025	snp	C/G/T	5.12582e-05	0.00506231	synonymous-codon, missense	RNF126	GRCh38.p7	19:651778	AGGGAACGTGGGGAT[C/G/T]TCGAAGCTGTCATCG	55658
rs780325896	snp	A/G	0.000286082	0.0119566	intron-variant	RNF126	GRCh38.p7	19:648532	GGGCGTGGGGGGCCT[A/G]CCGAGCCTTCAAGGG	55658
rs780515826	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:652028	CCCCGCTGGTGTGAG[A/G]TGCCTCGGTGGAAGT	55658
rs780696274	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:661706	CTGGGTCTCTACTCC[A/C]GGGGAACTGCACTGC	55658
rs780702807	snp	A/G	0.000102791	0.00716832	intron-variant	RNF126	GRCh38.p7	19:648306	GAGGCAGGGACGGGA[A/G]AAGGGGCAGGTTAGA	55658
rs780806467	snp	C/T	6.95918e-05	0.0058984	intron-variant	RNF126	GRCh38.p7	19:652334	CAGTGCCGGCTACCC[C/T]GTGCCCCCATGCGCC	55658
rs780986529	snp	A/G	0.000108944	0.00737972	missense, intron-variant	RNF126	GRCh38.p7	19:651654	GGCCGGTGGCCCGCC[A/G]CGTGGTGAGGCGGGC	55658
rs781039393	snp	A/G	1.8552e-05	0.0030456	intron-variant	RNF126	GRCh38.p7	19:652812	CCAGCCTCTTCAACA[A/G]GGGGCTGCATTACCT	55658
rs781073156	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:657073	GCCCCCACTGAGGGC[A/G]GGACGTAAGTCAGCT	55658
rs781265830	snp	A/G	3.51834e-05	0.0041941	intron-variant	RNF126	GRCh38.p7	19:652200	CCGAGCAAGGCTGAC[A/G]CGATCGGGAAGCACG	55658
rs781288497	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660108	CTGCCCCTGTGCCGT[C/T]GTCGCCTGAGCCCCC	55658
rs781494230	snp	A/G	1.65211e-05	0.00287407	missense	RNF126	GRCh38.p7	19:651732	CCCGCCGGCTCTCAG[A/G]GTCCCTGCCGTCGTC	55658
rs781544494	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:655069	GATCCCAGTACTTTG[C/G]GAAGCCAAGGTGGGC	55658
rs781585322	snp	C/T	2.76629e-05	0.00371896	utr-variant-3-prime	RNF126	GRCh38.p7	19:647939	CCCCAGAGGGGACCA[C/T]GTGGCCCACGCCTTC	55658
rs781698670	snp	A/G	1.73763e-05	0.00294752	synonymous-codon	RNF126	GRCh38.p7	19:651760	GTCAGCCTGCGCCCC[A/G]GGAGGGAACGTGGGG	55658
rs781719335	snp	A/C			intron-variant	RNF126	GRCh38.p7	19:654368	CGCCATCACCGGGGG[A/C]GCGGTGGCTCAGGCC	55658
rs796195266	in-del	-/AG			intron-variant	RNF126	GRCh38.p7	19:652811	TCCAGCCTCTTCAAC[-/AG]GGGGCTGCATTACCT	55658
rs796235227	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:660123	CGTCGCCTGAGCCCC[C/T]GACCGCAAGTGTGGC	55658
rs796309493	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:660128	CCTGAGCCCCCGACC[C/G]CAAGTGTGGCTCCCC	55658
rs796696653	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:654363	CGCTCCGCCATCACC[-/G]GGGGCGCGGTGGCTC	55658
rs796751238	snp	C/G			intron-variant	RNF126	GRCh38.p7	19:662343	GCACGCCCAGGCCCA[C/G]GGTCCTCTTCGGTGA	55658
rs796863090	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:650119	CAGGCTGGGGATGGG[A/G]ACAGGCACCCCCTCC	55658
rs797018050	snp	C/T			utr-variant-3-prime	RNF126	GRCh38.p7	19:647702	GGGGCCCACGTGGCC[C/T]GTCCTGGCGGCACCT	55658

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