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

RNF166

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs758013514	snp	C/T	0.000265781	0.0115247	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88706588	GAGCCGCCCCCGGCG[C/T]CGCGGCCCAGGTAAG	115992
rs758097672	in-del	-/G	7.45962e-05	0.00610676	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701431	AACCTGCAGGGCACA[-/G]GGGCCTGAGTGCCAG	115992
rs758107212	snp	A/G	6.5809e-05	0.00573586	intron-variant	RNF166	GRCh38.p7	16:88699091	GGGGATGTTGCTGGC[A/G]GGGCGGGGGTAGAGT	115992
rs758180011	snp	A/G			intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699983	CTGGAGAAGGGTAGC[A/G]GGAAACAGGTAAGGA	115992
rs758276830	snp	C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707456	TGGAACTTATGGGGA[C/T]AGTTGGAAGTGGGGC	115992
rs758353541	snp	C/T	1.66871e-05	0.00288847	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701356	GGGTCGAAGGGCAGG[C/T]GGCAGAGTGGGCACA	115992
rs758418264	snp	C/G/T	4.99225e-05	0.00499591	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701303	CTTTGTAGGATGAGA[C/G/T]CTGCTTCTCCACGTG	115992
rs758437683	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704660	ACAGATGAGAAGGTG[C/T]GGAACACACCTTCAA	115992
rs758441870	snp	C/T	0.000171792	0.00926641	missense	RNF166	GRCh38.p7	16:88698558	GCTGCAGGAAGTTGG[C/T]GCTCTTGTAGCTGGG	115992
rs758683841	snp	C/T			utr-variant-3-prime	RNF166	GRCh38.p7	16:88696898	CCTGAGCTCTGGCAG[C/T]TGCCCCACTGCTCCT	115992
rs758696494	snp	C/T	0.000227713	0.0106679	intron-variant	RNF166	GRCh38.p7	16:88698644	CAAGCCGAGCCGGAC[C/T]GCGGAGAGGCGGGGT	115992
rs758725595	snp	C/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704961	CGCCACTGCACTCCA[C/G]GCTGGGTGACAAGAG	115992
rs758733121	snp	C/T	1.65866e-05	0.00287976	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707201	TACGAGCCGGAGATG[C/T]CTTCTGCAGGTGAGG	115992
rs758734678	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703251	TTCTAGAATTGCATC[A/G]ATTGTTGCATAATTG	115992
rs758879134	snp	A/G			intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88700109	GCTTCGTGTGACTGA[A/G]GGGCAAGCTGGGGAT	115992
rs759032475	snp	A/G	1.74211e-05	0.00295132	intron-variant, missense, synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699710	CAGGACGAAATGTGC[A/G]CTCTCATCTTTGCCA	115992
rs759050597	snp	A/G	6.64194e-05	0.0057624	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699761	CAGGGAGGGCAAGGC[A/G]GTCCTGAGAATCTGG	115992
rs759140854	snp	C/T	1.66676e-05	0.00288679	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701247	GGCTCCAGGGCGGCC[C/T]AAGCAGGCGGGTACC	115992
rs759184061	snp	A/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696185	GGAGATCGAGGCTGT[A/G]GTGAGCTGATTGCAC	115992
rs759253176	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704772	AGACGGGCAGGTCAC[C/T]GGAGGTCAGGAGTTC	115992
rs759357714	snp	A/C/G	3.3226e-05	0.0040758	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707116	GTGTTTCTCTCTTCT[A/C/G]CCCCCTCCCATCTCC	115992
rs759441167	snp	C/G	5.88287e-05	0.00542318	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699126	GGCACGGCTAGGTGT[C/G]TAGGGGCTCTGCCTC	115992
rs759517336	snp	A/G	1.65762e-05	0.00287886	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707164	TGTGTGAAGTGCAAG[A/G]AAGCGCAGCCCGTTG	115992
rs759659253	snp	C/T	2.55249e-05	0.00357236	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699590	AACCGCCGAGGACAG[C/T]TCCTCTCCCTTGCCC	115992
rs759675710	snp	A/G	0.000186098	0.00964441	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696598	CGTGTTGCCCGGCCC[A/G]CCAAGCGGGCCCCTG	115992
rs759750452	in-del	-/A	0.000808407	0.0200886	intron-variant	RNF166	GRCh38.p7	16:88698365	CACAGAACCTGGGGG[-/A]ATGTGGCCACCTGAA	115992
rs759814786	snp	G/T	2.64694e-05	0.00363786	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701434	CTGCAGGGCACAGGG[G/T]CCTGAGTGCCAGCCC	115992
rs759905729	snp	A/G	0.000201025	0.0100236	intron-variant	RNF166	GRCh38.p7	16:88698635	CACTGGGGTCAAGCC[A/G]AGCCGGACCGCGGAG	115992
rs759967676	snp	A/C	5.88582e-05	0.00542454	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701448	GGCCTGAGTGCCAGC[A/C]CGCCCCTCGGGTCTC	115992
rs760023324	snp	C/T			downstream-variant-500B	RNF166	GRCh38.p7	16:88696153	GGAGGTCAAGGCGAG[C/T]GGACCACTTGAGCCC	115992
rs760077454	snp	A/G	7.41977e-05	0.00609043	intron-variant	RNF166	GRCh38.p7	16:88698953	GCGCAGGCGTCGCTT[A/G]GGGCAGGCACTGCTC	115992
rs760115160	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702232	GGCGCGAGAGCCCCC[A/G]GTGCAAACACAGAGA	115992
rs760165999	snp	C/G/T	0.000197492	0.00993514	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701456	TGCCAGCCCGCCCCT[C/G/T]GGGTCTCCCGAACCG	115992
rs760177678	snp	A/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696365	TCTGTGGGACCCTCC[A/G]TGGCTGAGTGAGGCT	115992
rs760198761	snp	A/T	1.66164e-05	0.00288235	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707242	GCTGAGACCCTGGCA[A/T]ACATGGCCTCGCTAG	115992
rs760235300	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703434	GAAGGTTGGCTGGGA[A/G]GAAGACAGCCTCGTC	115992
rs760444086	snp	A/C	1.65501e-05	0.00287659	intron-variant, missense	RNF166	GRCh38.p7	16:88699755	ACAGGGCAGGGAGGG[A/C]AAGGCGGTCCTGAGA	115992
rs760479873	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88700466	CCACAGCCTGCTCAG[C/T]CGCACCACTCTGGAG	115992
rs760504832	snp	A/G	2.34436e-05	0.00342363	intron-variant	RNF166	GRCh38.p7	16:88697675	GGGCTCGAGGGAGAC[A/G]GGAAGGAGAGGTCCC	115992
rs760679163	in-del	-/TAA			utr-variant-3-prime	RNF166	GRCh38.p7	16:88696534	TAAACTTTTTTTTTT[-/TAA]AAAAAAAAGACAGCA	115992
rs760806383	snp	C/T	3.32336e-05	0.00407624	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707109	GTGATCTGTGTTTCT[C/T]TCTTCTCCCCCCTCC	115992
rs760820740	snp	C/G	1.67711e-05	0.00289573	intron-variant	RNF166	GRCh38.p7	16:88699117	AGAGTGAGTGGCACG[C/G]CTAGGTGTCTAGGGG	115992
rs761046384	snp	A/C/T	3.33085e-05	0.00408085	intron-variant, utr-variant-5-prime, synonymous-codon, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701334	GGTGGCCTTGTCCAC[A/C/T]TTCTTGGGGTCGAAG	115992
rs761096828	snp	A/T	0.000186064	0.00964351	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696556	AAGACAGCAATAATT[A/T]ATGCCAAGAACAGAA	115992
rs761214789	snp	A/T	0.000179646	0.0094758	intron-variant	RNF166	GRCh38.p7	16:88698628	GAACAGGCACTGGGG[A/T]CAAGCCGAGCCGGAC	115992
rs761281563	snp	A/G	8.50521e-05	0.00652065	missense, synonymous-codon	RNF166	GRCh38.p7	16:88698503	GGCGGGATGCCTACC[A/G]CAAAGGTGTCGTAGG	115992
rs761404242	snp	A/C			intron-variant	RNF166	GRCh38.p7	16:88697915	TCCGAGGTGAGCAGG[A/C]CGGCCAGGGCTCCCT	115992
rs761523515	snp	C/T	3.8017e-05	0.00435971	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699746	ACCTAGGAGACAGGG[C/T]AGGGAGGGCAAGGCG	115992
rs761565958	snp	C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707325	GTACTTACTTTATTC[C/T]TGCTCCTGATGGGGT	115992
rs761579945	snp	C/T	3.32254e-05	0.00407573	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707236	GAGGTGGCTGAGACC[C/T]TGGCAAACATGGCCT	115992
rs761654310	snp	C/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697253	CCTTCTTCCCACGAG[C/G]GGGTATCATGGCTTT	115992
rs761661885	snp	A/G	1.71082e-05	0.00292469	missense, synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699674	TTGGGGCAGTTGGCC[A/G]TCTGCTCCTGGACCT	115992
rs761807417	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88705608	TCCTCTGTGGACCAG[C/T]CTGCCTGGCTACTCA	115992
rs761892065	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703492	AAGAGGGAACCCAGC[C/T]CGACTGGCAGGGCGG	115992
rs761922283	snp	C/G	2.99945e-05	0.00387251	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701451	CTGAGTGCCAGCCCG[C/G]CCCTCGGGTCTCCCG	115992
rs762199019	snp	C/T			downstream-variant-500B	RNF166	GRCh38.p7	16:88696109	CAGGAGGTGCTGAGG[C/T]GGCGCACACCTGTAG	115992
rs762251826	snp	A/G	3.33795e-05	0.00408517	intron-variant	RNF166	GRCh38.p7	16:88699107	GGGCGGGGGTAGAGT[A/G]AGTGGCACGGCTAGG	115992
rs762368655	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704877	TGCCTGTAATCCCAG[C/T]TACTCTGGAGGCTGA	115992
rs762369596	snp	C/G	1.66507e-05	0.00288532	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701325	CTCCACGTGGGTGGC[C/G]TTGTCCACCTTCTTG	115992
rs762379974	snp	C/T	3.44323e-05	0.00414909	intron-variant	RNF166	GRCh38.p7	16:88698490	GGAGGACGGTGCTGG[C/T]GGGATGCCTACCACA	115992
rs762435933	snp	C/T	1.66624e-05	0.00288633	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701255	GGCGGCCCAAGCAGG[C/T]GGGTACCTTTTTGTT	115992
rs762483336	snp	C/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707998	TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC	115992
rs762512613	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702957	TCATGGCAGGAGAAG[C/T]GGAAGCAGCTCAGGT	115992
rs762522116	snp	A/G	9.77947e-05	0.00699198	intron-variant	RNF166	GRCh38.p7	16:88698433	GACCCTGAGGCTGGC[A/G]AGGGGCCCGAGCAGG	115992
rs762788749	snp	A/T			intron-variant, synonymous-codon, missense	RNF166	GRCh38.p7	16:88697949	CTCTAACAATTTCCA[A/T]CCTGAGGCAGGCGGA	115992
rs762848854	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703810	GTCTCCCACACTGGC[C/T]GCTGCACAAGCTGAG	115992
rs762922489	snp	A/G	8.59646e-05	0.00655552	synonymous-codon, missense, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699655	GGGCACCACGGGGAC[A/G]AACTTGGGGCAGTTG	115992
rs763010285	snp	C/T	2.70772e-05	0.00367938	utr-variant-3-prime	RNF166	GRCh38.p7	16:88697543	ATCCCTGACCCCAGA[C/T]GCAGGCGGGTGGCTG	115992
rs763121988	snp	C/T			downstream-variant-500B	RNF166	GRCh38.p7	16:88696445	GACCTCCAACACAGA[C/T]AGCAGCTGGCGATTC	115992
rs763126790	snp	A/G	3.34711e-05	0.00409078	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701440	GGCACAGGGGCCTGA[A/G]TGCCAGCCCGCCCCT	115992
rs763136494	snp	A/C/G/T	0.000149274	0.00863797	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701450	CCTGAGTGCCAGCCC[A/C/G/T]CCCCTCGGGTCTCCC	115992
rs763226144	snp	A/C	6.628e-05	0.00575635	intron-variant	RNF166	GRCh38.p7	16:88698961	GTCGCTTGGGGCAGG[A/C]ACTGCTCACCACGCG	115992
rs763393981	snp	C/T	0.000164441	0.00906606	missense, synonymous-codon	RNF166	GRCh38.p7	16:88699038	TGCTGGTCCAGGTTG[C/T]GGGCACCACAGTACG	115992
rs763486774	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697220	GCTCGACTGCGGAGC[A/G]CGACTCGCGCGTCGG	115992
rs763608765	snp	A/G/T	0.000178667	0.00944996	intron-variant	RNF166	GRCh38.p7	16:88698491	GAGGACGGTGCTGGC[A/G/T]GGATGCCTACCACAA	115992
rs763663607	snp	G/T	3.31587e-05	0.00407164	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707183	CGCAGCCCGTTGTGG[G/T]GATACGAGCCGGAGA	115992
rs763804393	snp	A/G			intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701140	TCCTGGTGCAGGAGC[A/G]GAGACCGCGATTACT	115992
rs763896840	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703438	GTTGGCTGGGAGGAA[A/G]ACAGCCTCGTCCTCC	115992
rs764043009	in-del	-/C	8.84682e-05	0.00665028	intron-variant	RNF166	GRCh38.p7	16:88698932	GTCCCCCACAGGCCT[-/C]CCCTGGCGCAGGCGT	115992
rs764049498	snp	A/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696467	TGGCGATTCCACACC[A/G]TGGAGCACAAAAGCC	115992
rs764125122	snp	C/G			intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699342	CAGGAGCCGTCTCTC[C/G]GCCCATCCACCTGCT	115992
rs764129186	snp	A/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704837	TCTACTAAAAATACA[A/G]CAATTAGCCGGGCGT	115992
rs764274806	snp	C/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88696567	AATTAATGCCAAGAA[C/G]AGAAAAGAATGTTGA	115992
rs764311523	snp	A/C/G	7.34734e-05	0.00606072	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701442	CACAGGGGCCTGAGT[A/C/G]CCAGCCCGCCCCTCG	115992
rs764385570	snp	C/G	6.42859e-05	0.00566911	intron-variant	RNF166	GRCh38.p7	16:88698963	CGCTTGGGGCAGGCA[C/G]TGCTCACCACGCGGT	115992
rs764524945	snp	C/G	2.27146e-05	0.00336998	intron-variant, missense	RNF166	GRCh38.p7	16:88699765	GAGGGCAAGGCGGTC[C/G]TGAGAATCTGGAAGG	115992
rs764535512	snp	A/G			intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88704453	CCACAATTCCATGTG[A/G]TTCTGCATTCTGTGT	115992
rs764766797	snp	A/G	3.334e-05	0.00408276	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701249	CTCCAGGGCGGCCCA[A/G]GCAGGCGGGTACCTT	115992
rs764801802	snp	G/T	0.000342936	0.0130901	intron-variant	RNF166	GRCh38.p7	16:88698315	AGTGGCCACTCAAAC[G/T]CAGCTGCCATCACTC	115992
rs764812762	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701535	CAGGGGCAGCTCCCC[C/G]TACCGCTGTCGCCGT	115992
rs764956339	snp	A/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707872	CAACAGCTGGAGTGC[A/G]TGATCCCAGCTCACT	115992
rs765094331	snp	A/C			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703493	AGAGGGAACCCAGCC[A/C]GACTGGCAGGGCGGC	115992
rs765137655	in-del	-/TG			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707811	TTTTGTTGTTGTTGT[-/TG]TTTTTTTTGAGATGG	115992
rs765166146	snp	C/T	2.44945e-05	0.00349952	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699595	CCGAGGACAGTTCCT[C/T]TCCCTTGCCCGGCAG	115992
rs765181369	snp	A/G	0.000186064	0.00964351	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696617	AGCGGGCCCCTGCCC[A/G]GGCCCCCAAGCTCTG	115992
rs765208075	snp	A/G	5.99179e-05	0.00547315	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699128	CACGGCTAGGTGTCT[A/G]GGGGCTCTGCCTCCC	115992
rs765448505	snp	A/G	1.6766e-05	0.00289529	synonymous-codon, missense	RNF166	GRCh38.p7	16:88698540	TGTGTCGGTGAAGCA[A/G]GTGCTGCAGGAAGTT	115992
rs765495067	snp	A/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696113	AGGTGCTGAGGTGGC[A/G]CACACCTGTAGTCCC	115992
rs765510682	snp	A/C	2.76011e-05	0.0037148	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701436	GCAGGGCACAGGGGC[A/C]TGAGTGCCAGCCCGC	115992
rs765522049	snp	C/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696227	AGCCTGGGCAGCAGA[C/G]TGACACCCCACCTCT	115992
rs765547193	snp	A/C	2.22422e-05	0.00333476	intron-variant	RNF166	GRCh38.p7	16:88698638	TGGGGTCAAGCCGAG[A/C]CGGACCGCGGAGAGG	115992
rs765677213	snp	A/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704916	GATCACTTGAACCCA[A/G]GAGATGGAGGTTGCG	115992
rs765698103	snp	C/T			intron-variant, missense	RNF166	GRCh38.p7	16:88700056	AAGGAAGAGGCCAAG[C/T]GGAGGCCACTCAGAA	115992
rs765739941	snp	C/G/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88705629	TGGCTACTCAGTGAT[C/G/T]GGTGTGACTCAAGTT	115992
rs765847688	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702363	TCCCAGGAAGGCTAC[A/G]GCACCCGGGGGTGTA	115992
rs765854267	snp	A/G	3.3232e-05	0.00407614	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707243	CTGAGACCCTGGCAA[A/G]CATGGCCTCGCTAGC	115992
rs765935398	snp	A/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703233	TCTGGAGTGGGAAGA[A/T]TCTTCTAGAATTGCA	115992
rs765947541	snp	A/G	1.72892e-05	0.00294012	intron-variant, missense, synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699701	ACCTTCAGGCAGGAC[A/G]AAATGTGCACTCTCA	115992
rs765990449	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702929	GCCTCAGGGGACCCC[C/T]ATACTCAGGCACTCA	115992
rs766031358	snp	C/T	2.19089e-05	0.00330968	utr-variant-3-prime	RNF166	GRCh38.p7	16:88697566	GGTGGCTGCGCTTCC[C/T]TTCAGTTCTCAGAGA	115992
rs766233114	snp	C/G/T	4.9842e-05	0.00499189	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707111	GATCTGTGTTTCTCT[C/G/T]TTCTCCCCCCTCCCA	115992
rs766256345	snp	A/G			intron-variant, missense	RNF166	GRCh38.p7	16:88697962	CATCCTGAGGCAGGC[A/G]GAGCGTGGGTCCCGG	115992
rs766259207	snp	C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88708072	ACCTGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	115992
rs766316284	snp	C/T			intron-variant	RNF166	GRCh38.p7	16:88697698	GAGGTCCCCTCTGCC[C/T]ATCACCCACACAGGC	115992
rs766321027	snp	C/T	5.19521e-05	0.00509641	intron-variant	RNF166	GRCh38.p7	16:88699118	GAGTGAGTGGCACGG[C/T]TAGGTGTCTAGGGGC	115992
rs766327133	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706463	GCCGTCACGGCGCCA[C/G]TCCGACGTCATCGGG	115992
rs766384616	in-del	-/CACT	0.00018093	0.00950959	intron-variant	RNF166	GRCh38.p7	16:88698306	GCACCCTCTAGTGGC[-/CACT]CAAACTCAGCTGCCA	115992
rs766599021	snp	C/T	1.66454e-05	0.00288486	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701278	TTTTTGTTGCAGCCT[C/T]GACAGGGCGCTTTGT	115992
rs766641172	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703563	GGTGGGTGCTCTATC[A/G]GCCTAGTTTCCAGTG	115992
rs766938400	snp	A/C	0.00137322	0.0261673	intron-variant	RNF166	GRCh38.p7	16:88698629	AACAGGCACTGGGGT[A/C]AAGCCGAGCCGGACC	115992
rs766979235	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703162	GCAGAGAGAAACCCA[A/G]TGACCAGAAAGCAGA	115992
rs767078776	snp	A/G	1.72392e-05	0.00293586	intron-variant, synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699697	CTGGACCTTCAGGCA[A/G]GACGAAATGTGCACT	115992
rs767180760	snp	A/C/T	7.97902e-05	0.00631585	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699611	TCCCTTGCCCGGCAG[A/C/T]GTGCCTACCTGGGGA	115992
rs767214362	snp	C/T			downstream-variant-500B	RNF166	GRCh38.p7	16:88696195	GCTGTGGTGAGCTGA[C/T]TGCACCACTGCACTC	115992
rs767233110	snp	A/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704998	TCTGTCTCAAAAAAA[A/T]ATATTCCCGTTCAGA	115992
rs767452884	snp	C/T	0.000299088	0.0122252	utr-variant-5-prime, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706521	GTCTGCGACGGGACC[C/T]GGCGTGCCCATGTGT	115992
rs767572403	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701452	TGAGTGCCAGCCCGC[C/T]CCTCGGGTCTCCCGA	115992
rs767590252	snp	C/T			intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699253	ATGGCCTCCTGAGGA[C/T]ACACCCAGGACCCTC	115992
rs767646991	snp	A/G			intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88704357	GTGTGAAAAGCTCTT[A/G]CAGGACCCGCGGTGA	115992
rs767786499	in-del	-/GGCG	9.05428e-05	0.00672779	intron-variant	RNF166	GRCh38.p7	16:88698488	GGGGAGGACGGTGCT[-/GGCG]GGATGCCTACCACAA	115992
rs767901290	snp	A/G	1.66601e-05	0.00288614	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701256	GCGGCCCAAGCAGGC[A/G]GGTACCTTTTTGTTG	115992
rs767917540	snp	A/G	0.000291786	0.0120751	intron-variant	RNF166	GRCh38.p7	16:88698435	CCCTGAGGCTGGCGA[A/G]GGGCCCGAGCAGGAG	115992
rs767999357	snp	C/T	3.93647e-05	0.0044363	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701411	GCTGGAGACACTCCC[C/T]GCAGAACCTGCAGGG	115992
rs768223817	in-del	-/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703195	GTGGGTGCCAGGCGA[-/G]GGGGGAGAGTCCTGG	115992
rs768263640	snp	A/C/G/T	0.000426246	0.0145941	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701446	GGGGCCTGAGTGCCA[A/C/G/T]CCCGCCCCTCGGGTC	115992
rs768411827	snp	C/T	0.000163666	0.00904468	intron-variant	RNF166	GRCh38.p7	16:88698945	CTCCCCTGGCGCAGG[C/T]GTCGCTTGGGGCAGG	115992
rs768454413	snp	A/G	3.32242e-05	0.00407566	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707233	CTGGAGGTGGCTGAG[A/G]CCCTGGCAAACATGG	115992
rs768562428	snp	C/G/T	0.000325141	0.0127466	missense, synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699668	ACGAACTTGGGGCAG[C/G/T]TGGCCATCTGCTCCT	115992
rs768642405	snp	A/T	1.89267e-05	0.0030762	intron-variant, missense	RNF166	GRCh38.p7	16:88699742	GGTCACCTAGGAGAC[A/T]GGGCAGGGAGGGCAA	115992
rs768651491	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697016	TTCCTAGTCAAACAC[A/G]GATATTGCAATATGA	115992
rs768660780	snp	G/T	1.66913e-05	0.00288883	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701226	GGCTGCCCATCAAGT[G/T]ACCCCGGCTCCAGGG	115992
rs768662405	snp	A/G	9.84688e-05	0.00701603	intron-variant	RNF166	GRCh38.p7	16:88697644	TAGTCCTGGAGACAG[A/G]AAGGAGAGATGCACC	115992
rs768801464	snp	A/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706950	TTTTCTAGGCTAAAC[A/G]TCCCCCCAGAGCCTT	115992
rs769007645	snp	C/G/T	0.00121951	0.0246631	utr-variant-5-prime, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706502	TCGCGCTGTCGCCGC[C/G/T]ACAGTCTGCGACGGG	115992
rs769097469	snp	A/G	0.000199754	0.00999184	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707086	AGCCCACTAGGCGTG[A/G]GGAAGATGTGATCTG	115992
rs769560580	snp	A/G	1.80556e-05	0.00300457	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701396	GCACCTGCAGGCAGG[A/G]CTGGAGACACTCCCC	115992
rs769612812	snp	C/T			intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699578	CCAGAACGAGGAAAC[C/T]GCCGAGGACAGTTCC	115992
rs769704095	snp	A/C	1.65765e-05	0.00287888	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707168	TGAAGTGCAAGGAAG[A/C]GCAGCCCGTTGTGGT	115992
rs769725804	snp	G/T	1.66037e-05	0.00288125	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707224	AGGTGAGGCCTGGAG[G/T]TGGCTGAGACCCTGG	115992
rs769743656	snp	C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707030	CCGAGGTGCCTTTCT[C/T]TGACCCAACTCAGGG	115992
rs769819881	snp	A/G	1.72692e-05	0.00293842	synonymous-codon, missense, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699649	TGATGTGGGCACCAC[A/G]GGGACGAACTTGGGG	115992
rs769971310	snp	A/G	1.90685e-05	0.0030877	synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88697619	GAAGGCGGCCTCCTC[A/G]TCAATACTGTAGTCC	115992
rs769976883	snp	A/G	1.83802e-05	0.00303146	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699736	TGCCAGGGTCACCTA[A/G]GAGACAGGGCAGGGA	115992
rs770029724	snp	A/C	4.93717e-05	0.00496824	utr-variant-3-prime	RNF166	GRCh38.p7	16:88697537	GGGGACATCCCTGAC[A/C]CCAGACGCAGGCGGG	115992
rs770080195	in-del	-/TG	4.98749e-05	0.00499349	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707100	GGGGAAGATGTGATC[-/TG]TGTTTCTCTCTTCTC	115992
rs770292556	snp	A/G	0.000739814	0.0192187	intron-variant	RNF166	GRCh38.p7	16:88699096	TGTTGCTGGCGGGGC[A/G]GGGGTAGAGTGAGTG	115992
rs770397370	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697075	AAACGTGAAAAGATT[A/G]TCACACTGGATAATA	115992
rs770712335	snp	C/T	0.000103247	0.00718421	intron-variant	RNF166	GRCh38.p7	16:88698414	GCTTCCTCTGAACCC[C/T]GCGGACCCTGAGGCT	115992
rs770742526	snp	A/G	9.3471e-05	0.0068357	intron-variant	RNF166	GRCh38.p7	16:88698473	GATGAGGAGGGCGTG[A/G]GGGAGGACGGTGCTG	115992
rs770802510	snp	C/G	4.99247e-05	0.00499598	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701306	TGTAGGATGAGAGCT[C/G]CTTCTCCACGTGGGT	115992
rs770814246	snp	C/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704781	GGTCACCGGAGGTCA[C/G]GAGTTCGAGACCAGC	115992
rs770827976	snp	A/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704761	TTGGGAGGCTGAGAC[A/G]GGCAGGTCACCGGAG	115992
rs771036555	snp	A/C	1.65974e-05	0.0028807	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707217	CTTCTGCAGGTGAGG[A/C]CTGGAGGTGGCTGAG	115992
rs771068826	in-del	-/CCCTCCTGCTGC			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702152	CCTTGGGCTCGCACA[-/CCCTCCTGCTGC]CCCTCCCGCTCTGCA	115992
rs771163825	snp	C/G	2.63765e-05	0.00363147	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699585	GAGGAAACCGCCGAG[C/G]ACAGTTCCTCTCCCT	115992
rs771348379	snp	G/T	0.000558088	0.0166953	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696558	GACAGCAATAATTAA[G/T]GCCAAGAACAGAAAA	115992
rs771361888	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697093	ACACTGGATAATATA[A/G]AAAAGATGCCAGGGT	115992
rs771404230	snp	A/G	2.2155e-05	0.00332822	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701423	CCCCGCAGAACCTGC[A/G]GGGCACAGGGGCCTG	115992
rs771441929	snp	C/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697388	CGGCCCTGCTCTGGC[C/G]GCCTCGGCGGCTGGC	115992
rs771494150	snp	A/C/T	0.000182043	0.00953906	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701447	GGGCCTGAGTGCCAG[A/C/T]CCGCCCCTCGGGTCT	115992
rs771522074	snp	A/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707724	GTTTCCACTAGACTC[A/T]TAGCTCCCTGAAGGG	115992
rs771536133	in-del	-/C	3.32265e-05	0.0040758	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707115	GTGTTTCTCTCTTCT[-/C]CCCCCCTCCCATCTC	115992
rs771555941	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703719	AGGGCGATGGGTGTG[C/G]GGGCGTCGACAGCCT	115992
rs771683988	snp	C/T	3.16441e-05	0.00397757	synonymous-codon, missense	RNF166	GRCh38.p7	16:88699001	GCTGCGGTGGCTTTC[C/T]ACACAGTGCTTCACC	115992
rs771769918	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703354	TCGGCTGCACAGCAC[A/G]GCCACGGGCTGAGGG	115992
rs771831188	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88705181	CACTGGCCCTGCCAC[C/T]TCCGTGGGTGACCAG	115992
rs771872695	snp	A/G	3.3432e-05	0.00408838	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701232	CCATCAAGTGACCCC[A/G]GCTCCAGGGCGGCCC	115992
rs771875137	snp	C/T			intron-variant, stop-gained	RNF166	GRCh38.p7	16:88699819	TCAGGTGTCCAGGAC[C/T]AGAGAACTGTAAGCA	115992
rs771960416	snp	A/C	0.000106298	0.00728957	intron-variant	RNF166	GRCh38.p7	16:88698404	TCTGTTTCTGGCTTC[A/C]TCTGAACCCTGCGGA	115992
rs771991539	snp	A/G			intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701014	GGGTTCCCCTGGCCC[A/G]GGCTAGGCGGCTCTG	115992
rs772210109	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701832	TCCCGGCTCCACACT[C/G]TGGGGGATAAAACCT	115992
rs772251054	snp	C/T	3.31675e-05	0.00407218	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707128	TCTCCCCCCTCCCAT[C/T]TCCAAAGCCGTGAGC	115992
rs772302806	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703066	GCCCCACCACGCACC[A/G]GAAGGCCTGGAAAAC	115992
rs772318777	snp	C/T	1.66181e-05	0.00288249	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707106	GATGTGATCTGTGTT[C/T]CTCTCTTCTCCCCCC	115992
rs772642768	snp	C/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702798	TTCTCACCAGGCGCC[C/G]CAGCAGATATTTCCA	115992
rs772694412	snp	A/C/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88708406	TTTCAGGAGCCCAGA[A/C/G]GCAGCATGTACACGT	115992
rs772769044	snp	A/G	1.95624e-05	0.00312743	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699752	GAGACAGGGCAGGGA[A/G]GGCAAGGCGGTCCTG	115992
rs772900256	snp	C/T			missense	RNF166	GRCh38.p7	16:88698973	AGGCACTGCTCACCA[C/T]GCGGTTGGGGTCGCT	115992
rs772931374	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703141	TCCACTCACGCTCAA[C/T]GTCCAGCAGAGAGAA	115992
rs773194301	snp	C/T	5.80063e-05	0.00538515	intron-variant	RNF166	GRCh38.p7	16:88698407	GTTTCTGGCTTCCTC[C/T]GAACCCTGCGGACCC	115992
rs773224445	snp	C/T	4.98533e-05	0.00499241	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707107	ATGTGATCTGTGTTT[C/T]TCTCTTCTCCCCCCT	115992
rs773309426	snp	A/G/T	0.000267917	0.0115709	utr-variant-5-prime, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706527	GACGGGACCCGGCGT[A/G/T]CCCATGTGTCAGGTG	115992
rs773314285	snp	C/G			intron-variant	RNF166	GRCh38.p7	16:88697919	AGGTGAGCAGGCCGG[C/G]CAGGGCTCCCTGACC	115992
rs773500233	snp	A/C/G	4.7498e-05	0.00487307	intron-variant	RNF166	GRCh38.p7	16:88699116	TAGAGTGAGTGGCAC[A/C/G]GCTAGGTGTCTAGGG	115992
rs773603812	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703341	ACCAGGCCGGGGCTC[A/G]GCTGCACAGCACGGC	115992
rs773627300	in-del	-/T	0.402083	0.198421	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696524	ACATTTTATTTAAAC[-/T]TTTTTTTTTTAAAAA	115992
rs773647084	snp	A/C	3.33084e-05	0.00408082	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701332	TGGGTGGCCTTGTCC[A/C]CCTTCTTGGGGTCGA	115992
rs773664599	snp	A/G			downstream-variant-500B	RNF166	GRCh38.p7	16:88696171	ACCACTTGAGCCCAG[A/G]AGATCGAGGCTGTGG	115992
rs773713792	in-del	-/TC	1.66192e-05	0.00288259	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707106	GATGTGATCTGTGTT[-/TC]TCTCTTCTCCCCCCT	115992
rs773736959	snp	A/G	2.02435e-05	0.00318141	intron-variant, utr-variant-5-prime, synonymous-codon, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701412	CTGGAGACACTCCCC[A/G]CAGAACCTGCAGGGC	115992
rs773957072	snp	G/T	0.000175147	0.00935642	intron-variant	RNF166	GRCh38.p7	16:88698623	ACCTGGAACAGGCAC[G/T]GGGGTCAAGCCGAGC	115992
rs773989512	snp	C/T	3.32209e-05	0.00407546	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707234	TGGAGGTGGCTGAGA[C/T]CCTGGCAAACATGGC	115992
rs774046417	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702651	ATTCCCACAGAGCCA[C/T]CACCTGGCTGGTGGC	115992
rs774077067	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88704237	ATTTGCATGCATGCC[G/T]TAGCAACACCAACAA	115992
rs774276333	snp	G/T	1.89536e-05	0.00307838	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699743	GTCACCTAGGAGACA[G/T]GGCAGGGAGGGCAAG	115992
rs774283390	in-del	-/GTG	1.65787e-05	0.00287907	cds-indel, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707179	GAAGCGCAGCCCGTT[-/GTG]GTGATACGAGCCGGA	115992
rs774290344	snp	A/T	0.000197472	0.00993465	intron-variant	RNF166	GRCh38.p7	16:88697653	AGACAGGAAGGAGAG[A/T]TGCACCGGGCTCGAG	115992
rs774396921	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703119	CGTCCCACCCGTGTC[A/G]TGGGGGTCCACTCAC	115992
rs774484513	in-del	-/ACAC			intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699251	CATGGCCTCCTGAGG[-/ACAC]ACACACCCAGGACCC	115992
rs774568078	in-del	-/C	0.000147591	0.00858915	intron-variant	RNF166	GRCh38.p7	16:88698346	CCCACCTGCAGGCAG[-/C]CCCCACAGAACCTGG	115992
rs774749131	snp	C/G	1.66322e-05	0.00288371	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707091	ACTAGGCGTGGGGAA[C/G]ATGTGATCTGTGTTT	115992
rs774786014	snp	A/C/T	1.6638e-05	0.00288422	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707252	TGGCAAACATGGCCT[A/C/T]GCTAGCAGACAGGAT	115992
rs774834548	snp	A/T	1.66649e-05	0.00288655	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701252	CAGGGCGGCCCAAGC[A/T]GGCGGGTACCTTTTT	115992
rs775013391	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704946	GGTGAGCCGAGATGG[C/T]GCCACTGCACTCCAG	115992
rs775185972	snp	A/G			intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699908	AGGCACTGAGCAGCC[A/G]CTACTCCATGGCCAA	115992
rs775238649	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703722	GCGATGGGTGTGGGG[G/T]CGTCGACAGCCTTAC	115992
rs775328559	snp	C/G	1.65781e-05	0.00287902	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707174	GCAAGGAAGCGCAGC[C/G]CGTTGTGGTGATACG	115992
rs775345205	snp	A/C			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88700415	GAGAGAAGAACTCTG[A/C]GCAGGGAGAGACGGG	115992
rs775351264	snp	C/T	2.39644e-05	0.00346145	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699597	GAGGACAGTTCCTCT[C/T]CCTTGCCCGGCAGCG	115992
rs775484839	snp	A/G	2.47448e-05	0.00351736	utr-variant-3-prime	RNF166	GRCh38.p7	16:88697540	GACATCCCTGACCCC[A/G]GACGCAGGCGGGTGG	115992
rs775778938	snp	C/T	9.78617e-05	0.00699438	missense, utr-variant-3-prime	RNF166	GRCh38.p7	16:88697627	CCTCCTCGTCAATAC[C/T]GTAGTCCTGGAGACA	115992
rs775937223	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702284	CCACATCTGGCCTTG[C/T]GAGGAGCACTGTGGG	115992
rs775989264	snp	A/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707846	CTCCCTCTGTCACCC[A/G]GGCTGGAGTGCAACA	115992
rs776085695	snp	A/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704857	TAGCCGGGCGTGGTG[A/G]CGGGTGCCTGTAATC	115992
rs776617473	snp	G/T	0.000185667	0.00963321	intron-variant	RNF166	GRCh38.p7	16:88698476	GAGGAGGGCGTGGGG[G/T]AGGACGGTGCTGGCG	115992
rs776632807	snp	C/T	5.2293e-05	0.0051131	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699587	GGAAACCGCCGAGGA[C/T]AGTTCCTCTCCCTTG	115992
rs776660681	snp	A/C	1.6577e-05	0.00287893	missense, upstream-variant-2KB, utr-variant-5-prime	CTU2, RNF166	GRCh38.p7	16:88707162	AGTGTGTGAAGTGCA[A/C]GGAAGCGCAGCCCGT	115992
rs776661601	snp	A/G	5.48381e-05	0.00523603	intron-variant	RNF166	GRCh38.p7	16:88699124	GTGGCACGGCTAGGT[A/G]TCTAGGGGCTCTGCC	115992
rs776715518	snp	C/G			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88705466	GGGCTGGCAGCTCCA[C/G]AATACTTGAGCACAG	115992
rs776849931	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703113	CAAGCACGTCCCACC[C/T]GTGTCGTGGGGGTCC	115992
rs777037459	snp	C/G	2.55242e-05	0.00357232	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701432	ACCTGCAGGGCACAG[C/G]GGCCTGAGTGCCAGC	115992
rs777056424	snp	C/T			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697405	CCTCGGCGGCTGGCC[C/T]GTATTCAGGCCCGGA	115992
rs777098190	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702857	TTGAGCCGGGGGGGC[C/T]GCCTACTTCACCCGT	115992
rs777315475	snp	A/G	6.12764e-05	0.00553484	synonymous-codon, missense	RNF166	GRCh38.p7	16:88699004	GCGGTGGCTTTCCAC[A/G]CAGTGCTTCACCAGC	115992
rs777345741	snp	C/T			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697321	CCTGCCCAAGTAGGC[C/T]GCCTGCTCGGCCAGA	115992
rs777399729	snp	A/G	3.3189e-05	0.0040735	intron-variant	RNF166	GRCh38.p7	16:88699092	GGGATGTTGCTGGCG[A/G]GGCGGGGGTAGAGTG	115992
rs777426512	snp	C/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703034	GGAAAGGGCGTTCGG[C/T]CGGGAAGAGGCGTGC	115992
rs777571800	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88700307	CCGGGAGACACAGCC[A/G]CATCTGAAGACCCAG	115992
rs777652606	snp	C/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707719	CAGTTGTTTCCACTA[C/G]ACTCATAGCTCCCTG	115992
rs777894895	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704679	ACACACCTTCAAACA[C/T]CCGCTACCTGCTCAC	115992
rs778085350	snp	G/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88708224	TATGCTAGGCCCTTG[G/T]GGCCAGAAGGGCTTT	115992
rs778096830	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703649	ACAGGAAGTTCCTGT[C/G]TGCGCCCACCCAGGG	115992
rs778279236	in-del	-/AG	3.90678e-05	0.00441955	intron-variant	RNF166	GRCh38.p7	16:88699102	TGGCGGGGCGGGGGT[-/AG]AGTGAGTGGCACGGC	115992
rs778339042	snp	C/T	3.54799e-05	0.00421173	intron-variant, utr-variant-5-prime, synonymous-codon, missense, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699721	GTGCACTCTCATCTT[C/T]GCCAGGGTCACCTAG	115992
rs778439474	snp	A/T	2.04882e-05	0.00320058	synonymous-codon, utr-variant-3-prime	RNF166	GRCh38.p7	16:88697577	TTCCCTTCAGTTCTC[A/T]GAGAGAGACAGGGCC	115992
rs778478075	snp	A/G			intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88700997	CTGGCCACAACCCAC[A/G]TGGGTTCCCCTGGCC	115992
rs778532036	snp	C/T	3.62115e-05	0.00425493	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701470	TCGGGTCTCCCGAAC[C/T]GCAGGCCTTGCTCGG	115992
rs778532973	snp	C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706834	CTGCCGCTGACAGTG[C/T]TGTCCTTATTCGGAG	115992
rs778639362	snp	A/G	1.65831e-05	0.00287945	missense	RNF166	GRCh38.p7	16:88698991	GGTTGGGGTCGCTGC[A/G]GTGGCTTTCCACACA	115992
rs778960567	snp	C/T			intron-variant, missense	RNF166	GRCh38.p7	16:88699826	TCCAGGACCAGAGAA[C/T]TGTAAGCAAGCGTCT	115992
rs779088906	snp	A/G	6.65701e-05	0.00576894	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701287	CAGCCTCGACAGGGC[A/G]CTTTGTAGGATGAGA	115992
rs779122062	snp	C/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88702792	CCCGAGTTCTCACCA[C/G]GCGCCCCAGCAGATA	115992
rs779156521	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701755	CCAGGTTCACGTTCA[A/C]GTGGCGACAACACCT	115992
rs779195497	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88704035	ACAGCTCCTGCTGGG[A/C]CCCCAGGGGGCCTCC	115992
rs779247845	snp	C/T			splice-donor-variant	RNF166	GRCh38.p7	16:88698501	CTGGCGGGATGCCTA[C/T]CACAAAGGTGTCGTA	115992
rs779279853	snp	A/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703048	GCCGGGAAGAGGCGT[A/G]CAGCCCCACCACGCA	115992
rs779391434	snp	C/T	0.000428633	0.0146333	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696741	CCTTCTCTGCCGGCC[C/T]CGCCTCTGCTGGGAG	115992
rs779409585	snp	C/G			intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699454	GTATGCCAGGGAGGG[C/G]AGCACAGGAGCCTTC	115992
rs779472657	snp	C/T	4.97525e-05	0.00498736	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707125	TCTTCTCCCCCCTCC[C/T]ATCTCCAAAGCCGTG	115992
rs779483688	snp	C/T	0.000519615	0.0161102	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696525	ACATTTTATTTAAAC[C/T]TTTTTTTTTAAAAAA	115992
rs779502342	snp	A/G	1.87696e-05	0.00306341	intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701402	GCAGGCAGGGCTGGA[A/G]ACACTCCCCGCAGAA	115992
rs779574960	snp	A/C	5.72393e-05	0.00534943	intron-variant, downstream-variant-500B	RNF166	GRCh38.p7	16:88699615	TTGCCCGGCAGCGTG[A/C]CTACCTGGGGATAGG	115992
rs779813952	snp	A/C/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706930	TATGTGCCCCCTGAG[A/C/T]CGGCTTTTCTAGGCT	115992
rs779896624	in-del	-/G	2.97517e-05	0.00385681	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701452	GAGTGCCAGCCCGCC[-/G]CCTCGGGTCTCCCGA	115992
rs779935611	snp	C/T	0.000176788	0.00940014	intron-variant	RNF166	GRCh38.p7	16:88698932	GTCCCCCACAGGCCT[C/T]CCCTGGCGCAGGCGT	115992
rs779993059	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701682	GAGCCGTCACTATGG[A/C]TGTCCCCGCGAGTGG	115992
rs779993929	snp	A/G	1.64765e-05	0.00287019	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707261	TGGCCTCGCTAGCAG[A/G]CAGGATAGCCGCAAC	115992
rs780149855	snp	C/T	0.000428418	0.0146296	intron-variant	RNF166	GRCh38.p7	16:88698352	TGCAGGCAGCCCCCA[C/T]AGAACCTGGGGGAAT	115992
rs780160968	snp	A/G	1.84418e-05	0.00303654	intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88699737	GCCAGGGTCACCTAG[A/G]AGACAGGGCAGGGAG	115992
rs780247777	snp	C/T	5.00931e-05	0.0050044	intron-variant, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701217	GTGGGCTGAGGCTGC[C/T]CATCAAGTGACCCCG	115992
rs780330497	snp	C/G			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703073	CACGCACCGGAAGGC[C/G]TGGAAAACAGTGCAG	115992
rs780437510	snp	C/T			intron-variant, synonymous-codon	RNF166	GRCh38.p7	16:88700130	AGCTGGGGATGCTTC[C/T]GTGGAGGCAGGGCGC	115992
rs780438470	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88696952	ATGCTTGTTTTGATT[A/G]TTTTCTTAAAAAATA	115992
rs780443303	snp	A/C/T	0.000116085	0.0076178	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707123	TCTCTTCTCCCCCCT[A/C/T]CCATCTCCAAAGCCG	115992
rs780539868	snp	G/T	0.000108161	0.00735314	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88706629	CGGACCCGCCAGGCC[G/T]CCCCTCGCCTTCCCG	115992
rs780582235	snp	C/G			intron-variant, missense	RNF166	GRCh38.p7	16:88700227	CCTCCTGGACTCAAG[C/G]TCGGCACCCAGCTCT	115992
rs780637828	snp	C/G	1.66443e-05	0.00288477	intron-variant	RNF166	GRCh38.p7	16:88699099	TGCTGGCGGGGCGGG[C/G]GTAGAGTGAGTGGCA	115992
rs780824263	snp	G/T	0.00117256	0.0241848	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696711	CCAAGGCCAGGACTC[G/T]GGGTGGAGGAGGCCC	115992
rs780963589	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88701691	CTATGGCTGTCCCCG[C/T]GAGTGGGCCAGAGGA	115992
rs781000719	snp	C/T			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704605	CCTACGGGAGGCTTT[C/T]CTAAAACAAGGCCTA	115992
rs781033694	snp	A/G			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88708172	CAAGAACACCAGGCT[A/G]CCGGCAGAATTCACT	115992
rs781077044	in-del	-/A	0.258532	0.249854	utr-variant-3-prime	RNF166	GRCh38.p7	16:88696535	TAAACTTTTTTTTTT[-/A]AAAAAAAGACAGCAA	115992
rs781093876	snp	C/G/T			intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707597	GAAAGTTTTTAATCT[C/G/T]GTGTGAGATGCTTGT	115992
rs781185214	snp	C/T	1.69642e-05	0.00291236	intron-variant, utr-variant-5-prime, synonymous-codon, upstream-variant-2KB	RNF166	GRCh38.p7	16:88701373	GCAGAGTGGGCACAG[C/T]GGGGATGGCACCTGC	115992
rs781275177	snp	A/G	3.52193e-05	0.00419624	missense, synonymous-codon	RNF166	GRCh38.p7	16:88698593	CCCCAGGGCATTGCC[A/G]AGCAGATGGGGCACA	115992
rs781294632	snp	C/T	1.80517e-05	0.00300425	intron-variant, utr-variant-5-prime, missense, utr-variant-3-prime	RNF166	GRCh38.p7	16:88699729	TCATCTTTGCCAGGG[C/T]CACCTAGGAGACAGG	115992
rs781295018	snp	G/T	0.0790817	0.182447	intron-variant	RNF166	GRCh38.p7	16:88698658	CCGCGGAGAGGCGGG[G/T]TAGCCGCAGTAGGAC	115992
rs781306227	snp	C/G	1.65996e-05	0.00288089	intron-variant, upstream-variant-2KB	CTU2, RNF166	GRCh38.p7	16:88707218	TTCTGCAGGTGAGGC[C/G]TGGAGGTGGCTGAGA	115992
rs781518161	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703684	GTGCTGAGCAGCTTC[C/T]CAGCTGAAGGAAGTG	115992
rs781690380	snp	A/G			utr-variant-3-prime	RNF166	GRCh38.p7	16:88697026	AACACAGATATTGCA[A/G]TATGAAGAGTAACTG	115992
rs781717404	snp	A/G	0.000156165	0.00883504	intron-variant	RNF166	GRCh38.p7	16:88698338	CATCACTCCCCACCT[A/G]CAGGCAGCCCCCACA	115992
rs781721586	snp	C/T			intron-variant	RNF166	GRCh38.p7	16:88698673	GTAGCCGCAGTAGGA[C/T]TGGGGGCCCTCCACT	115992
rs781738876	snp	C/G	0.000650406	0.0180217	upstream-variant-2KB, missense	CTU2, RNF166	GRCh38.p7	16:88706292	GCGGCTGCCGCTGCT[C/G]AGCCGAGGCCACCAG	115992
rs796126172	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF166	GRCh38.p7	16:88703889	CACCCTCAGCAAGCC[C/T]CACAGCTGTCCTGCA	115992
rs796138331	snp	C/G			intron-variant	RNF166	GRCh38.p7	16:88698742	CAGACCTGGAGGCGC[C/G]TGTCCCGGTGACAAG	115992
rs796335222	snp	G/T			intron-variant, utr-variant-5-prime	RNF166	GRCh38.p7	16:88700434	GGGAGAGACGGGAGG[G/T]GCCCAAGCACCCAAG	115992
rs796606951	in-del	-/T			utr-variant-3-prime	RNF166	GRCh38.p7	16:88696534	TTAAACTTTTTTTTT[-/T]AAAAAAAAGACAGCA	115992
rs796619927	in-del	-/A			upstream-variant-2KB, intron-variant	CTU2, RNF166	GRCh38.p7	16:88704991	GCAAGACTCTGTCTC[-/A]AAAAAAAATATTCCC	115992
rs796759551	snp	G/T			intron-variant	RNF166	GRCh38.p7	16:88698364	CCACAGAACCTGGGG[G/T]AATGTGGCCACCTGA	115992

Page 1 | 2