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

RNF182

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs374468291	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13948396	ACACAATAATTTAAG[A/T]TAACAATTATAACTA	221687
rs374478978	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13938145	ACTGGGACTACAGGC[A/G]CCCGCCACCATGCCT	221687
rs374495576	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930872	GATTGTACAGAGTTG[A/G]TAGATTTAAAAACAT	221687
rs374498394	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954517	AACAAAAATTCATAA[A/G]CTTTCTGAGAACATT	221687
rs374504855	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13937796	CAGTGTATGAAAGTT[C/G]TAGTTGTTTCTCATT	221687
rs374505223	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950613	ACAATTCTCGTGCCT[C/T]AACCTCCCGAGTACC	221687
rs374549696	snp	A/G	7.02001e-05	0.00592411	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977101	CCCACCTGGCATAAG[A/G]TTGCACACATAATTC	221687
rs374559512	snp	A/G	1.64781e-05	0.00287033	missense	RNF182	GRCh38.p7	6:13977397	TTGTAAACTTGACTT[A/G]TGGAGGCAAAGGGAA	221687
rs374564778	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13972175	CTGGGCATGGTGGAA[C/T]GCGCCTGTAGTCTCA	221687
rs374573097	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952493	CGGGAGGGATGCTAA[C/T]CCTTCTGAGTTGGGT	221687
rs374592333	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13941884	TAAAATAACATTATA[C/T]ATTATTGCTGTTTTA	221687
rs374661820	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13927766	TTGCACTGTGATAAC[A/G/T]TGATTACTGGTTGGT	221687
rs374665734	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13942374	TGAGACAAAATCTTG[C/T]TCTGTGGCCCAGGCT	221687
rs374744684	snp	A/T	0.474453	0.110094	intron-variant	RNF182	GRCh38.p7	6:13930123	TATTTGGAAAAATAT[A/T]TGGAAAATATTCCAA	221687
rs374787024	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956085	ACTTCACATAATGTC[A/G]TTCAGACTTATTCAT	221687
rs374893497	in-del	-/A	0.00201126	0.0316478	intron-variant	RNF182	GRCh38.p7	6:13960435	TCACTTGAGGCCAGG[-/A]ATTTGAGACCAGTCT	221687
rs374901718	snp	C/T	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13952590	TTGGTGCTGTGCAGA[C/T]GATTTTCCTTTGGTT	221687
rs375023915	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13946625	TCCTATGACTAAAAA[C/T]GTCTAGCCTCCTGGG	221687
rs375076953	in-del	-/TATTTGG			intron-variant	RNF182	GRCh38.p7	6:13930120	AAATATTTGGAAAAA[-/TATTTGG]AAAATATTCCAAAAA	221687
rs375239683	snp	C/G	0.00557542	0.0525036	intron-variant	RNF182	GRCh38.p7	6:13942424	TCAGCTCACTGCAAC[C/G]TCTGCCTCCTGGGCT	221687
rs375320688	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13938813	ATGTATTTGTCTAAT[A/C]AAGTGTCTTACATAA	221687
rs375337240	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13962159	TATTAACAGTAATGA[C/G]AGTCTTTTAAGCTCT	221687
rs375461021	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13947646	GGATGTCCCAAGATA[C/T]TTGGGGCTCCTGGGC	221687
rs375707368	snp	A/G	0.0150606	0.0854603	intron-variant	RNF182	GRCh38.p7	6:13972019	AAAGGGAAACAGAGC[A/G]GCTGGGTGCAGTGGC	221687
rs375751649	snp	A/G	8.23839e-05	0.00641757	missense	RNF182	GRCh38.p7	6:13977366	GTTAGTAGCCTGCCC[A/G]ATGACAACAACATCC	221687
rs375830874	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943148	GTAGTTTCTAAATTA[C/T]AAAGTACTGTTAATG	221687
rs375983907	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13934350	CTTTAGGCCGTGCCC[A/G]CCAGTGTTTGAGATA	221687
rs376193117	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13928557	GCTTATTTTAAAAAT[G/T]ATTTGGTTAATTTGT	221687
rs376306596	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13931661	TTCTCTTTTTTTTTT[-/T]AATGTTCAAGGCCAG	221687
rs376317342	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13967685	TGGCAATAAAAAATA[A/C]ATTTTATTTAGAAAT	221687
rs376422545	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13941701	ACATTGTGTTTTACT[C/T]TTTTGACTGTTATCC	221687
rs376429574	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13929924	GCATTTCTTCATAGC[A/G]TATTGTGACATGTAC	221687
rs376459249	snp	C/T	4.94303e-05	0.00497119	missense	RNF182	GRCh38.p7	6:13977666	TTTCAGACATCCATC[C/T]GGGTGTTAGTGTGGT	221687
rs376495863	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13937115	TACTTGTTTTGTGTT[G/T]TATGTATCTTGTATA	221687
rs376597879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13973525	GGAGATAATTGAATC[A/G]TGGAGTCAGTTTCCC	221687
rs376666892	snp	C/T	7.01496e-05	0.00592198	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977102	CCACCTGGCATAAGA[C/T]TGCACACATAATTCA	221687
rs376677480	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954287	CAGAAAACAATTGCA[A/G]AGTAATTCCTTACTG	221687
rs376715431	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13949384	CAGATCTCTAACATT[C/T]ATTTGTACACAAAAA	221687
rs376733532	snp	A/G	4.94678e-05	0.00497307	missense	RNF182	GRCh38.p7	6:13977789	GTCCCTTCGAGCCTC[A/G]TTATTCTTATGGTGT	221687
rs376736422	snp	G/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978576	TGTTTTCCTCTCTCC[G/T]CAGTCTTATCTGAGA	221687
rs376817539	multinucleotide-polymorphism	CC/TG			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978386	TACTTGTTTCCTCTG[CC/TG]CATTCTCCCTTGCCA	221687
rs376930946	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926484	TATTGGAAACTAAAG[A/G]ATTGAAGTTGCAATT	221687
rs377038473	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13946544	CTGGGTCTGTTATTT[A/C]CTGGGTTTGTTAAGT	221687
rs377168490	snp	A/G	1.64735e-05	0.00286993	missense	RNF182	GRCh38.p7	6:13977259	GGGTTTGTGCCAAAT[A/G]CCTCTACAAGATCAT	221687
rs377228548	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13956665	AATGTTCTTTCTCTG[A/C]TTAATGTATCTTGGC	221687
rs377235860	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13955640	GCAACCACAGGGCCC[G/T]TGATGCATTATGTGC	221687
rs377290770	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13969744	AGCTCAAGCTAATTT[A/G]TGAGAATAATAGTAG	221687
rs377292669	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13937759	GTTGTCCAGGTGGTT[A/T]TATCGGCGACATTCT	221687
rs377295507	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13953764	CTGTGGGTCCTGCTC[A/C]TGCGACATTGACCAT	221687
rs377354589	snp	C/T	0.00438332	0.0466095	intron-variant	RNF182	GRCh38.p7	6:13950621	CGTGCCTCAACCTCC[C/T]GAGTACCTGGGATTA	221687
rs377357528	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13964862	GTGCGTCCTTTGGAG[C/G]AGGAGACCTTGGAAG	221687
rs377394153	in-del	-/CTAT			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923325	ATAAGAAATCAATAT[-/CTAT]GAATTTTATATATTT	221687
rs377413130	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942489	TGGGACTGACTACAC[A/G]TGCCACCACACCTGG	221687
rs377509800	in-del	-/TC			intron-variant	RNF182	GRCh38.p7	6:13951815	CATAGGCAAAGACTC[-/TC]AGTTTTGCAAGATGC	221687
rs377541446	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13946751	CATTTATAAGGGGAC[C/T]CTTAATCCTGAAGGT	221687
rs377556092	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924781	GCGTGTTTGTGGTGG[C/T]GGCGGCCCATCGGGG	221687
rs377682293	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924389	CAAAGCTTGCTAAAA[A/G]AGAGAGGAGGAGGAG	221687
rs386406226	in-del	-/TT			intron-variant	RNF182	GRCh38.p7	6:13950499	GACAAAACAGGTACT[-/TT]TTTTTTTTTTTTTTT	221687
rs386406227	in-del	-/TT			intron-variant	RNF182	GRCh38.p7	6:13950516	TTTTTTTTTTTTTTT[-/TT]TGACAGAGTCCTGCT	221687
rs386697323	in-del	AAAATGCAACGAT/TATTTGGAAAATATTCC			intron-variant	RNF182	GRCh38.p7	6:13930120	AAATATTTGGAAAAA[lengthTooLong]AAAAAATAATTCAAA	221687
rs386697324	multinucleotide-polymorphism	ATA/GTG			intron-variant	RNF182	GRCh38.p7	6:13966834	TGTGTGCGCGTGCGT[ATA/GTG]TGTGTGTGTGTGTGT	221687
rs397719571	in-del	-/ATT/ATTATT/ATTATTATTATT	0	0	intron-variant	RNF182	GRCh38.p7	6:13946182	ATTATTATTATTATT[-/ATT/ATTATT/ATTATTATTATT]TTGAGATAGAGTCCT	221687
rs397727543	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13935314	ATGTCTTTTTTTTTT[-/T]CTTTTTGCCTAAAGT	221687
rs397767716	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13969842	AGTTAGGAATACCAG[-/G]CTTCATATATTTGAA	221687
rs398000540	in-del	-/T	0	0	intron-variant	RNF182	GRCh38.p7	6:13933439	ATGAGGCAGGAGGAT[-/T]GCTTGAGCTCAGGAG	221687
rs527257766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966824	CTGTTTTGTGTGTGT[A/G]CGCGTGCGTGTGTGT	221687
rs527307846	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974567	ATTTTCAAGGAAATA[A/T]TTTAGGTTCACATAA	221687
rs527434560	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967266	GGTATAAAGGTTGAT[A/G]TTTAAGTTAAAGGCA	221687
rs527447591	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953380	CTGCCCTGGGTGTGT[G/T]TGTATGGTGGGGGGC	221687
rs527568741	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947396	TTGGCAAAATAAATT[G/T]TAGTCTTATTGTATG	221687
rs527606865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946614	AACTGTAAATATCCT[A/G]TGACTAAAAATGTCT	221687
rs527654107	snp	C/T	0.00358779	0.0422022	intron-variant	RNF182	GRCh38.p7	6:13958796	AGTAATTGGAGAGGA[C/T]CTCCTTGAGGACTTC	221687
rs527687554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936404	TTAGAACTCAGGATA[A/G]TATCTCTACTGAGAT	221687
rs527690982	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13957951	GATTGTGGACAAATA[G/T]TTATCAATTGGAGAT	221687
rs527723997	in-del	-/A	0.474723	0.109542	intron-variant	RNF182	GRCh38.p7	6:13930127	TGGAAAAATATTTGG[-/A]AAATATTCCAAAAAA	221687
rs527817628	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952150	AAAGCATTGTCTGTT[C/G]TGGGGCTGGGAGGCG	221687
rs527835505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938269	TAATCTGCCAACCTC[A/G]CCCTCCCAAAGTGCT	221687
rs527989375	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938834	TCTTACATAATCCCA[A/G]CACTTTGGGAGGCCG	221687
rs528056992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948572	TCAAATAAGTCAAAT[A/G]TGCCATTATTGGACT	221687
rs528166627	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13941458	TTTCTTTTATAAGCC[A/G]CATATAGCTGGCTTT	221687
rs528178169	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943267	TTATTACCATGTGCA[C/T]AGAGGTGGTTCCTGC	221687
rs528219555	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940916	CTAGCTTAATCCAGC[G/T]ATTGTCAAAGAACAC	221687
rs528221957	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949003	TTAATAAAATCATAC[A/G]GACAAAATCTACTCA	221687
rs528224311	snp	G/T			utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974277	CTGTCACCTGGTCTT[G/T]CCCAGAAGAGCCGTT	221687
rs528284492	snp	A/G	0.000346024	0.0131488	synonymous-codon	RNF182	GRCh38.p7	6:13977545	GAGAGAGAGCTCCCC[A/G]TCCCTGAGCTCCACT	221687
rs528292219	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13947750	TTCTTAGGGGCTTTA[A/G]TTGGCTCTATAAATG	221687
rs528349024	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928061	GTTTAGTGACATGGA[C/T]TATTAATAGTGATTG	221687
rs528405012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935867	TGAGTGTATTAGTCC[A/G]TTCTCACATTGCTAT	221687
rs528426969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940245	AGCAAATGATTTTCC[A/G]CATTTATCGAGATGA	221687
rs528528137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13976094	TGAAATAAAGTAGAT[A/G]AGTAAGTGAATGTTG	221687
rs528591182	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933828	TTCGAGACCAACCTG[C/G]CCAATGTGGTGAAAC	221687
rs528593854	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979844	CTTGTGTCTCCGTGT[A/G]TTGTGGCAGTCTTTT	221687
rs528751916	snp	A/T	0.00119737	0.0244387	downstream-variant-500B	RNF182	GRCh38.p7	6:13980280	GAAAAATTAGGGGAG[A/T]TGAAATAAAAATATC	221687
rs528934951	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13966766	GGAACCTGTCCCCAC[C/T]CCCCCACCCCCCCAC	221687
rs529001697	snp	G/T	0.474723	0.109542	intron-variant	RNF182	GRCh38.p7	6:13930131	AAAATATTTGGAAAA[G/T]ATTCCAAAAAATAAT	221687
rs529040532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966020	GTACTCTCCTGAGGA[C/T]GGAGCTCAGATAAAA	221687
rs529052999	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13971078	GCCTGCACTAAGTCT[C/G]CTTGGACACTGTTTT	221687
rs529075995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965300	TACAGAACAAAAATA[C/T]AAAGGAATGGAAACC	221687
rs529076263	snp	A/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13973676	CCTTCACCTTCTGCC[A/T]TGATTGTGAGGCCTC	221687
rs529095688	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973634	TTGTCTCTTGCCTGC[C/T]GCCATGTAAGACATG	221687
rs529234902	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13959003	GCTTCCTATCTTGCC[A/G]TGTGATCTCTGCAGA	221687
rs529235229	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13943787	GGGAGAGACCTCAGT[C/G]TTACCGGAGCTTAAC	221687
rs529245282	in-del	-/ATG	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13965226	GAACTGAAGGTGATA[-/ATG]ATCATTCTTGGGGCT	221687
rs529258797	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13963751	CACACTCTTAATGTT[A/G]GTCAAAGCAAGTCAC	221687
rs529329626	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970687	CCATAGTGGTTGTAC[A/T]AATTTATATTCTTAC	221687
rs529412614	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13950446	ACTAAATGTCTAAAA[A/G]TCATGTGAACTAAAT	221687
rs529455774	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949736	TCTTCACAAAAATGG[A/G]TAAGTATAAAACTTG	221687
rs529492012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957261	GTTGAATATATGTCA[A/G]TCAACAATGCCACAT	221687
rs529500742	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979431	AGGTACAGTGCGCCC[A/G]TTCCAACTGGAATAG	221687
rs529552507	snp	C/T	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13937054	ATCAGATTTGAGTTT[C/T]AGAAAGTCTCTCATG	221687
rs529797796	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13961566	CCTAAATATAGGGTG[C/T]GGAGTACCTGGTTTT	221687
rs529850841	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946783	GCAGAGGGATAGAAA[C/T]TTATCTTCTGTAGCT	221687
rs529892003	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923401	CCACATTATTTAACC[A/G]TATCACTATTGATGG	221687
rs530231929	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961233	CTGATACTGTGTTCA[A/G]TGCATATTCTGTCTA	221687
rs530300126	snp	A/T	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13934142	TTGAAATTAAATATG[A/T]TGTAGATTTCAGCTT	221687
rs530308813	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924683	TAGGATGCGAATACC[A/G]CTTGGCCCTGGGCTC	221687
rs530335206	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13955181	ATGCAGCGTTGGACG[A/G]GATGTGCATGAATGG	221687
rs530344412	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932781	CATGACAATTGTGTA[C/T]AGGCTGTTCCAATTA	221687
rs530370396	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975168	CTAGGACTGTGTGTG[A/G]TGACCAGGATAGAAC	221687
rs530375251	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930242	TAAAGTACATGGCAG[A/G]ATGTACATAGGTTAT	221687
rs530422320	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932838	TAAAAAGTAATAATA[C/G]AAGTCTGATTTTCCT	221687
rs530442898	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923810	TAGTAAACCCAGAAA[A/G]CATCAGCTACCGTGG	221687
rs530492281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941558	TATAATTGGGTTTAA[A/G]CTTCCCATTGTACTA	221687
rs530502091	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949443	TCTATAGGTTTCTTT[A/G/T]ACTTCATTCTGGCCT	221687
rs530649717	snp	C/G/T	0.00318978	0.0398085	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978157	AGACAGACGGCAGGG[C/G/T]TGTGGTGTGTTATAC	221687
rs530653670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942368	TTTTTTTGAGACAAA[A/G]TCTTGCTCTGTGGCC	221687
rs530668281	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13948459	TTATAGTAGTTTTGC[A/C]TAATTTTGGAACACA	221687
rs530725030	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978778	TACTTTTTTTCCCTA[C/T]TATATTTTTGGTTCT	221687
rs530783691	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963865	TTGTACAGGTCTGTG[A/G]AGAATTATTGCAGCC	221687
rs530855888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13929092	CCCAATTAACTAAAA[C/T]GTGACTCTCTTGAAT	221687
rs530893701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925701	ATTGCTTTTGTTTCT[A/G]GAAGGTATTGTGTTC	221687
rs530964434	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13976191	TCTGTGTTTACTTCT[C/T]TTTCTTGGGACTTAG	221687
rs530992181	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962912	TTCATATGGACAGTG[C/G]AGTAATACATAGCAT	221687
rs531031212	snp	A/G	0	0	intron-variant	RNF182	GRCh38.p7	6:13969849	GAATACCAGCTTCAT[A/G]TATTTGAAAATGTAT	221687
rs531057153	in-del	-/A	0.00358779	0.0422022	intron-variant	RNF182	GRCh38.p7	6:13959860	AGCCCTCTGGAACTC[-/A]AGAGGGAAGGGATAG	221687
rs531153369	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955794	AGTGTGGCTCACACC[A/T]GTAATTGCAGCACTT	221687
rs531187836	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13926986	CCATGGTGAATTTAG[A/C]ACAGTAAGGACCGGT	221687
rs531226286	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13972716	GGGTGCACAGAAGTC[A/G]AGAATTGAGGTTTGG	221687
rs531317428	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13973814	ATGTAGTCTAATCAC[C/T]GCCAGAGTTTTCATC	221687
rs531348280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966100	ACAAAAGAATAGTCT[A/G]TAGGACTACTGGGTT	221687
rs531385837	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959855	ACTGTAAGCCCTCTG[A/G]AACTCAGAGGGAAGG	221687
rs531422607	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966686	GAAGATTGCTTGACC[A/C]CGCGGGGTGGAGGTT	221687
rs531457419	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922520	TCAGTAGCTAATTCA[C/T]ATGTGGCTAGCAGTT	221687
rs531470533	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13927119	AATCAACAATCATGT[A/G]TTGCATGCACTGCTT	221687
rs531475181	in-del	-/CACT	0.00358779	0.0422022	intron-variant	RNF182	GRCh38.p7	6:13974726	TTACGTATTCATAAA[-/CACT]CACATGTCTACTCTA	221687
rs531503830	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13960772	ATCTACTTAAGTTTG[A/C]AATTGTAGAAATGGT	221687
rs531869002	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979840	TAAACTTGTGTCTCC[A/G]TGTATTGTGGCAGTC	221687
rs531882368	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938133	GGTCTCTGCGTAACT[A/G]GGACTACAGGCGCCC	221687
rs531888221	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933875	ATACAAAAATTAGCT[A/G]GGCCTGGTGGCATGC	221687
rs531985456	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957916	TAATAGATACTTTTG[A/G]TGAGCCTAAACCTGA	221687
rs532099249	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13948481	TGGAACACATACCAA[A/T]AACACATTTAAATAA	221687
rs532110572	snp	A/G	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13953996	GAGAAAGCTTTGCTA[A/G]TGATTTTATTTTTAT	221687
rs532142584	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923853	ATCATTGACATTCCT[C/T]TGGTGATTCACAAAT	221687
rs532151164	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961609	TCCTGAACATTTATT[G/T]GTTTAAAACTGCTGG	221687
rs532155654	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13926541	GGGCTTGTTTTTAAA[C/T]TGAATTTTACCTGTG	221687
rs532160155	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940865	TTACTTAATTTCCAA[C/T]GGTTTAGGATATTCT	221687
rs532273709	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926577	TTCACAGATGCTCTG[C/G]TAAATACTCTTTCAT	221687
rs532275298	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13954908	GTGGAGGGGCTCTAC[G/T]CTTCCTGCTGCATGG	221687
rs532374348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946455	CAGGCATGAGCCACC[A/G]TACCTGACTGCAAAA	221687
rs532395841	snp	C/T	0.00199481	0.0315187	utr-variant-5-prime	RNF182	GRCh38.p7	6:13976953	TTTGAGACAGAGTTA[C/T]ATGCAGAAGTTGAAA	221687
rs532548749	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13945424	TGAGGAGATGATGGT[A/G]CTTCAGCAGTGCCCC	221687
rs532554992	snp	A/G	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13960186	CCATTTGCCTTTACA[A/G]TCAGCCTCTGCTTTC	221687
rs532579190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975950	TACTGAAAATTGAGA[A/G]CTGACTGTGCATATG	221687
rs532690711	snp	G/T	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13932056	ATCTTGGACTTCCCA[G/T]TTCCCAGAACAGTGA	221687
rs532701269	snp	G/T	0.00914312	0.0669923	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924707	TGGGCTCGCTCCGCT[G/T]TAGCCTTCCCCTCTC	221687
rs532709370	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930876	GTACAGAGTTGGTAG[A/G]TTTAAAAACATGATT	221687
rs532714936	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933808	AGGTCACCTGAGGTC[A/G]GTAGTTCGAGACCAA	221687
rs532716065	snp	C/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13925472	TTTTTACGAATCTCT[C/G]AAAAGTGAGCCCATT	221687
rs532719687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967704	TTATTTAGAAATTTA[A/G]GAAAAGTATATAACC	221687
rs532758711	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933377	AAAAATTAGCTGGGC[A/G]TGGTGGTACGCACGT	221687
rs532761821	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13975206	TGTTCTTTGGCTGTC[A/G]TCCTGAAGATGTTCA	221687
rs532892648	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943119	CTAATGGCTACCTTA[C/T]CTAAATGGTGAAAGT	221687
rs532910040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936114	TGAGAATTCTGTCGC[A/G]AGATAGCACTATGGG	221687
rs532960505	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13964626	TTTGTGAAAGCTGAG[G/T]GTGGGGAGTGGGGAG	221687
rs533063661	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936837	GTGGTAAGTGTGGGT[A/G]AAAGAGCTATAAAGA	221687
rs533117692	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13927348	CATGGTTTAGCCACC[C/T]GGTGGAAGCAGGCAA	221687
rs533125572	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13939031	GAGGTTGTAGTGAGC[C/T]AAGATTGCACCACTG	221687
rs533161423	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13943577	GCTATATTTTGCATA[A/C]ATGCCTGTCCCCCTC	221687
rs533192879	snp	C/T	3.29674e-05	0.00405988	synonymous-codon	RNF182	GRCh38.p7	6:13977441	GAGAACCCTACTGAG[C/T]TGCTGCTCACCCCCA	221687
rs533241863	in-del	-/C	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13946248	CTCAGCTCACTGCAA[-/C]CTCTGCCTCCTGGGT	221687
rs533291030	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963001	TGAGCTCTACTTATT[G/T]TGACTTTTTTTGTCC	221687
rs533300320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965223	AATGAACTGAAGGTG[A/G]TAATGATCATTCTTG	221687
rs533318771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956620	GTGAGCCAATGCTCC[C/T]GGCCTGTCCTTTGCG	221687
rs533485581	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949492	TGGTTATAAGAAAAA[A/G]TTACGGAAAAAGACA	221687
rs533509231	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970595	TTCTTTTTCTTTGGA[C/T]AGATACCAAGTAGAA	221687
rs533531683	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959240	ATGACATTTCACATT[A/G]AGCAAACAGCCTAAA	221687
rs533538915	in-del	-/AG	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13926022	AATATGAAAGAAAAC[-/AG]ATACATTTTCAGAAA	221687
rs533836565	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932196	CTTGGTGATTGTGAG[G/T]ATTAAATGAATTAAC	221687
rs534021352	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13929708	AATATGATCACTTTC[A/T]GTTACGTTAACCCAA	221687
rs534024405	snp	A/G	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937779	GGCGACATTCTCAAC[A/G]TCAGTGTATGAAAGT	221687
rs534112230	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931653	GACCTTTTTTTCTCT[C/T]TTTTTTTTAATGTTC	221687
rs534161923	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13934060	AAATGTGGCCTTACC[-/A]AAAAAAGTAATGTTG	221687
rs534184571	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13950823	TTTTTTTGAGATAGA[G/T]TCTTGTTCTGTCACC	221687
rs534249428	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979422	GTGTGATGCAGGTAC[A/C]GTGCGCCCATTCCAA	221687
rs534392098	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13972982	CATTTGGAAAAGCTG[C/T]AGACATTCAATGCCA	221687
rs534410578	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13938013	TTACTGTTTTTTTTT[-/G]TTTTTTTTTTTTTTG	221687
rs534417293	in-del	-/GT/GTAT	0.029116	0.117091	intron-variant	RNF182	GRCh38.p7	6:13966831	TGTGTGTGCGCGTGC[-/GT/GTAT]GTGTGTGTGTGTGTG	221687
rs534431439	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13980004	TTGTTATTATTTCCA[A/G]ATTTAGAAGTTTGAT	221687
rs534456297	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965598	AGCAAATTACTTACC[A/G]TGAAGAAGTATCACA	221687
rs534464143	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936456	GTAAATTTACATGGT[C/T]GTGGTTGATTGGTCT	221687
rs534552399	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13968903	TGTAATACTAAGTAG[A/G]AACCTAGATCTAAAA	221687
rs534604571	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947702	TGCTACAGGTCAGGA[G/T]CCCTGTACAAGGCTC	221687
rs534620356	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939838	GTGAGCCACTGTGCC[C/T]GGGCATAAATGCATT	221687
rs534706436	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934553	TTTACAACAGTTGTA[A/G]TAGTTCCAAAGGTGG	221687
rs534723487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974875	ACATGACTTCACATA[C/T]CTCAGTCCTTTCTAT	221687
rs534770285	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13967724	AGTATATAACCTTTT[G/T]AAAATTTATTAATTT	221687
rs534840969	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977004	TTCTTTCACTACTTA[C/T]CCTGCCTTTTTGCAT	221687
rs534844471	snp	C/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978357	ACTCTCTGTGGTCGG[C/T]GATCCCATTGAGATA	221687
rs534861199	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13945742	TCCATTACTGCTGTG[C/T]CTTAATTTCATCTTG	221687
rs534899564	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973354	AAATGAGTTAAGACA[C/T]TGGGGGACTGTTGGG	221687
rs534930853	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13960973	TTCTTATTAATCATG[A/G]TCTTAAATTATATCT	221687
rs534970920	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13924210	GCAGTGTGGCAGCAG[C/T]TGAGATCCATACTGC	221687
rs534978193	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13949727	GTACGATATCTTCAC[-/A]AAAAATGGGTAAGTA	221687
rs535016465	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966971	CCTTCTGAGTAGCTG[G/T]GACCACAGGCGTGCA	221687
rs535079970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971659	CAGAGACAGAAAGAT[A/G]TGGGGAAGTTTGGAA	221687
rs535103173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964007	AAGTGGGGAAGAAGA[C/T]CCAAAAACAGTTCAA	221687
rs535114057	snp	C/G	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13971067	GCCACTCCATAGCCT[C/G]CACTAAGTCTGCTTG	221687
rs535164085	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956986	ACTAGTAAATCACCT[A/G]TCCACTGTGTGACCG	221687
rs535210338	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13934616	TGTCATAGGTAGTTT[G/T]CCATTTAGATAGGAT	221687
rs535215421	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953724	GGGAAGGCATAGATG[C/T]GCCTTCTCTGCATTC	221687
rs535247244	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13937577	ATCATTTACTGTTCA[C/T]AGACATTTGGGTTGT	221687
rs535379370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954078	TAATGAATCCCTTTT[C/T]ACTTATCACTCAGCC	221687
rs535387874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947040	CAACTGTAAAGCGAA[A/G]TCAGTAAAATTGTCT	221687
rs535425957	in-del	-/AG	0.00438332	0.0466095	intron-variant	RNF182	GRCh38.p7	6:13968130	GAAATTAAAAGTAAC[-/AG]AAAGGATAAATACAT	221687
rs535443533	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13948729	TTATAAAATAGAATC[A/T]CAGGTCACTGTAAGT	221687
rs535482957	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932304	AGAAACAAAAATCTA[A/G]TTTTCTTTAGGCCTT	221687
rs535494612	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964678	GGCTTGGCTGGTACC[A/C/G]AGGGCTGGCATCCAT	221687
rs535505973	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955339	GGTTGAAATCCTTCT[A/G]TAAAAAGAATTTTAC	221687
rs535535073	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940298	ATTTTGTCAATATGG[C/T]AATCACATTTTAAAA	221687
rs535573738	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13968330	AGAAGAAATGGATTT[G/T]TTCTTTGTCAAATAT	221687
rs535601956	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949175	TTTGGCATCTTCAGC[C/T]TACCAAAACTGTGTG	221687
rs535624147	snp	A/C	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13942630	TACAGGTGTGAGCCA[A/C]CACCCCTGGCCAGTT	221687
rs535633478	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13950985	TATATTTAGTAGAGA[C/T]GGGGTGTCACCATGT	221687
rs535644618	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935616	CAGAACATTTGATGA[A/T]CCAAAAAGATAGCAC	221687
rs535750500	snp	A/C/T	3.29458e-05	0.00405857	missense, synonymous-codon	RNF182	GRCh38.p7	6:13977701	AGGTTTGCTCTACTT[A/C/T]AGCTCCTTACCCTTA	221687
rs535798618	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951712	TTACCTTTCTCTGAG[C/T]GGCTCTGATAGTCTT	221687
rs535805724	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13927780	CATGATTACTGGTTG[A/G]TAATTTAGCATCTAG	221687
rs535985473	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945712	AACAGTAAAATGTTT[A/G]TTCCCTTGTTATATT	221687
rs536008624	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939711	ACCACGCCTGGCTAA[G/T]TTTTTGTATTTTTAG	221687
rs536140816	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928505	AAGTTACCAGTTAAT[A/T]TTGTAATGTTTTTTT	221687
rs536153348	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF182	GRCh38.p7	6:13925115	CCCGCAGTCCTGGAC[G/T]GCGCCGGGCCGCCCA	221687
rs536171553	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13945392	GCAAATAACCTTAAA[C/T]GTTGGAATTGCCCTT	221687
rs536179499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936186	CCTACCACCAGGCCC[C/T]GCCTCCAACATTGGG	221687
rs536342875	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931551	TTTCCTTGATAACTC[C/G]TGGGGGGGAAAAAGG	221687
rs536405327	in-del	-/G	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13948935	ATCTTGTTCAAAAGA[-/G]AAAGCCAAATTTCAC	221687
rs536405516	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922835	GCTAAACCTCTTTTG[G/T]AAAAATGAATGTCTG	221687
rs536417149	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932407	TTTGACTAAACTTTA[A/G]TTCAAATTGAACAGA	221687
rs536418333	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924800	GGCCCATCGGGGGTC[C/T]TTGTCCTCTCCGAAT	221687
rs536517499	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13941788	TCCTTCCGTGATGGT[A/G]TAGTGTTATTAGAAT	221687
rs536555760	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13969566	ATCCTAGGTAGACAA[C/T]AACAACAGGTGTCCA	221687
rs536614873	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13974786	AATTTTGCCTAGTTA[C/T]CTTCACTGGCTGTTT	221687
rs536783714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13930652	GAAAAGTAGGACTAA[A/G]TAAGAGACAGGTGTT	221687
rs536880193	snp	C/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13974123	AATCATAATAAGATA[C/G]ATGAAACTTTTTTTT	221687
rs536883694	in-del	-/C	0.0333695	0.124785	intron-variant	RNF182	GRCh38.p7	6:13966764	AGGAACCTGTCCCCA[-/C]CCCCCCCACCCCCCC	221687
rs537016244	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941457	GTTTCTTTTATAAGC[C/G]GCATATAGCTGGCTT	221687
rs537018394	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934663	TGATCCACGCATGAG[C/G]TCTTAATGCTGGCTG	221687
rs537051428	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945203	AAAAAGCCATGACCC[A/G]GAAAGTTTAAGTGAT	221687
rs537079544	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967848	TACAGGCGTGAGCCA[C/T]CATGCCTGGCCCTGT	221687
rs537089246	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13949852	AAGAGTAGATCAGTG[C/T]TCTAAGAAAACCCTG	221687
rs537106823	snp	A/G	1.64773e-05	0.00287026	missense	RNF182	GRCh38.p7	6:13977567	AGCTCCACTCCTGTG[A/G]TAGAATTTTATAGGC	221687
rs537220864	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953464	ACTGGGTGAGGATGG[A/G]ATTTTGGGGCTGTCA	221687
rs537328974	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13945676	GTTAAGACCTATTAG[A/T]TTATGCTATTTTTTG	221687
rs537466552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964818	TGTGTGTGTTCCACA[A/G]GAGACCAAGGAGAAA	221687
rs537560902	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13953528	GAACAGAGTGGAGGA[A/G]GAGTCCAGTGTTTTA	221687
rs537585337	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951022	GGCTGGTCTTGAACA[C/G]CTGGCCTCAGGTGAT	221687
rs537722591	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF182	GRCh38.p7	6:13980173	AAGGGGACCTAACCC[A/G]TCACACTTTTAAAAG	221687
rs537790939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940559	TTTATCAGTGAACTT[A/G]TTTTGACTTTTTTTT	221687
rs537792873	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948605	AGGGGACCTAATATC[G/T]AAAAGGATTATCAAG	221687
rs537834112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941951	CATTCCTTCATGTAA[A/G]TCTGTGTTTCCCTTT	221687
rs537834455	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13939440	TTAGATTTGTTCTTT[C/T]TGTTGTTATTGCAAA	221687
rs537873649	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949261	GACACCAGTTGTTTC[C/G]TCTGCTCCCAGACTT	221687
rs537996838	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942767	TGTTCTATTTGACTC[C/T]TAAACTCTTTTTCCT	221687
rs538059864	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936215	GGAATTACAATTCAA[A/C]ATGAGATTTGGGTGG	221687
rs538126930	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13930845	TAAAAGGCTAATAAA[A/T]AGCTTATCCAAGATT	221687
rs538207450	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13928187	AGTGCTTGGGGAAAA[G/T]GTATACTTTTATACA	221687
rs538210234	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939436	TTCATTAGATTTGTT[A/C]TTTTTGTTGTTATTG	221687
rs538221091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949804	CCAACGTTAAACTTA[C/T]AAAAGTTTTAAAACT	221687
rs538244648	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13931379	CCCTCAGGGTCAGAG[A/C]AACATGCTTTTTGCT	221687
rs538311382	snp	A/C	0.00874735	0.0655527	intron-variant	RNF182	GRCh38.p7	6:13964367	ATCTTTATGTAATAG[A/C]CGCTGAACATGCTTA	221687
rs538398366	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934045	AAAAATTAAAAAAAA[C/G]AAATGTGGCCTTACC	221687
rs538509791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968747	ATAAATAAATAAATA[C/T]GTCTGATGACCTTTG	221687
rs538559813	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13925786	AAAGCACCTCTGGAG[A/G]CAGGTAGCTGGGCGG	221687
rs538642812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953557	TATATTCACGAGTCA[C/T]GGAATAGGCAGTGTG	221687
rs538718405	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940309	ATGGTAATCACATTT[A/T]AAAAAAATGTTAGAA	221687
rs538749852	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13937209	AAAAGTGCACGAATC[A/G]TAAGGATATATAGCT	221687
rs538777222	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925172	ACTTCGGGCCGAGCG[C/G]CGCCGGGGCCCGCGC	221687
rs538816691	snp	G/T	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13967970	GATAGAGTGAAAGCT[G/T]TAGCCAGTGGAAACA	221687
rs538821585	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971329	CTCTCTTGCCTGTCA[C/T]CACATAAGATGTGCC	221687
rs538863016	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975460	TGAAATACAGGCATA[A/C]ATATACTGTATTTGA	221687
rs538877312	snp	G/T	0.0103295	0.0711199	intron-variant	RNF182	GRCh38.p7	6:13966840	CGCGTGCGTGTGTGT[G/T]TGTGTGTGTGTGTTT	221687
rs538932044	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13955370	CTCATCAATTATTTG[A/G]TTACTTTAAAGGCAT	221687
rs538948999	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959361	GAGGCCAGATTATAC[A/G]GTACCTTGCTGTGTA	221687
rs539014103	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974238	TGTTGGCTGCATTTC[C/T]AGGGATGCTACCAGA	221687
rs539045535	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13938401	TACAGAATTCTTCCA[C/T]ACTGTAGCTTGCTTT	221687
rs539089326	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966430	AATTTTTAGAATTCA[A/T]TAGATGTTTTAATTG	221687
rs539110824	snp	C/G			upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924578	CAGGAGAAAGGTGTG[C/G]TGGTGGTAGTGGTGG	221687
rs539181521	in-del	-/CAT			intron-variant	RNF182	GRCh38.p7	6:13962475	TCAAAGAATTTAAGA[-/CAT]CATAGAAACTGATAA	221687
rs539215814	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13965711	AGGGTTTGGTCTAGG[C/T]CCTACTTGCTCACCA	221687
rs539393497	snp	A/G	0.00358779	0.0422022	intron-variant	RNF182	GRCh38.p7	6:13937140	TGTATAGACATAGGA[A/G]GCATTACTTTTATTT	221687
rs539430803	in-del	-/AAATGTAACATTGAGT	0.00199481	0.0315187	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979722	TGTTCGTTTTGTTTG[-/AAATGTAACATTGAGT]AAATTGGTGAGTTAT	221687
rs539552991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928298	TTATGGAGTATGGTT[C/T]TGGACATCAGTCATC	221687
rs539582089	in-del	-/A	0.00478085	0.0486577	intron-variant	RNF182	GRCh38.p7	6:13933352	AGATCCCACCTCTAC[-/A]AAAAAATGCAAAAAT	221687
rs539618735	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956910	GTAACAAGCACCACC[C/T]CCCGCCCCCCACCAT	221687
rs539634889	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963919	CATGATAGGGGCTAG[G/T]GCAAAGAGTATTTAG	221687
rs539718380	snp	A/G	3.32552e-05	0.00407756	missense	RNF182	GRCh38.p7	6:13977147	CCTCCTGAAGACACT[A/G]CGGAGTCTCAGGCCT	221687
rs539782661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949854	GAGTAGATCAGTGCT[C/T]TAAGAAAACCCTGTT	221687
rs539837178	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969319	GCAGTCAGGAGCTTT[C/G]AGAAGTCCGGTTTGG	221687
rs539857992	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951221	TTTTTTATTTGCCAG[A/T]TTTAAGTTTCTTAAC	221687
rs539869289	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943130	CTTATCTAAATGGTG[A/G]AAGTAGTTTCTAAAT	221687
rs539888901	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13932702	GAAATCTATTACACA[-/T]TTTGAACTAGAATCA	221687
rs539960352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948144	TTCCTGTTTTTCTCA[A/G]TATTTATGAATACAT	221687
rs539991111	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949109	GATGGCTGCCACTGC[C/G]TTTGCCAGTGCAGTG	221687
rs540058228	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938086	GCTCACTGCAAACTC[C/T]GCCTACCGGGTTCAC	221687
rs540084854	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972472	AATGGGGAAAATGTC[A/T]CTGCATATCAGAGGT	221687
rs540109726	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974303	CCGTTCTTAGAGGCA[A/G]GACTTGATGAAGGCT	221687
rs540152869	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941716	CTTTTGACTGTTATC[C/G]TAGAGATTATAACAT	221687
rs540233168	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936420	TATCTCTACTGAGAT[G/T]CAATTATTCTTTGGT	221687
rs540343461	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963660	AGGCTAGCCTGGGCT[C/T]CTTTGATGGTGGTCT	221687
rs540397653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13930931	TTTGACTATGATTGC[C/T]TTGTTAATTACCAGC	221687
rs540445897	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943914	CAGTGTGGGTTTGTT[A/G]ATTGGTGTTTATCTG	221687
rs540485069	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13950357	ACAAGTCAAATAATT[A/G]TAAAAAATGTCATAG	221687
rs540525721	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923098	ATTTGAAAAAGCCAA[A/T]CAAACCAAATATGTG	221687
rs540562812	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978764	TATAAATTCATCAAT[A/G]CTTTTTTTCCCTATT	221687
rs540593491	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924601	AGTGGTGGAGGGTGT[C/G]TGTGGGGGGGATGGT	221687
rs540677437	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932670	CCTAAACATTTCAAT[A/C]AAAATAAATCATATC	221687
rs540697097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971219	GAGATAATTGAATTA[C/T]GGGGGCAGTTTCCCC	221687
rs540738775	in-del	-/TTT	0.00755907	0.0610114	intron-variant	RNF182	GRCh38.p7	6:13969101	TCAGGCTTGTCTCTG[-/TTT]TTTTTTGTTGTTGTT	221687
rs540756757	snp	C/T	0.00795532	0.062565	intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925282	GAGCGCCCGCGCGGG[C/T]TGCACCTGCTCAGGG	221687
rs540875578	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13929608	AGACACTTTTCTAAG[A/C]ACTTCAGAAATATCA	221687
rs540889338	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13947405	TAAATTTTAGTCTTA[C/T]TGTATGTGGACTGAT	221687
rs540889443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954650	CCCTTACAGTGTGGC[A/G]CAGGAAACTGAAAGA	221687
rs540946879	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13966121	CTACTGGGTTGGTTT[C/T]AGAGAGAAAAAAGAC	221687
rs540976414	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13934857	TAGGGATTTGAGTGA[C/T]GAGAAGATTTGATCA	221687
rs540991233	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13969575	AGACAATAACAACAG[A/G]TGTCCACTGGAGGGA	221687
rs541064506	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959552	TTCTGCAATGAACAA[G/T]GTCAAAACCTGGATT	221687
rs541069521	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975067	TGTTGTAAGAGCCTT[A/G]TGCTCAGCAGGGAAT	221687
rs541103462	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966575	TGAGACCAGCCTGGG[A/C]AACATGGCAAAACCC	221687
rs541131020	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13975704	CTCTGTTAGTGCAGT[A/G]TGATCCATAGCAAAT	221687
rs541452096	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13958837	CTGCTGTGGTTTTGG[A/G]TATTTGTTACTTCTA	221687
rs541512661	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13932499	TTTAAATCGCATGTT[A/T]CTTTAATGTATTTAT	221687
rs541545630	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13943095	TTATTTAATTACATT[C/G]AGGGAATACTAATGG	221687
rs541597163	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938888	AGGAGTTTGAGACCA[A/G]CCTGGCCAACATGGT	221687
rs541622512	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946143	TTTAAAGCAAAACAT[C/T]ATTATTATTATTATT	221687
rs541668347	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953018	TTGAGATGGAATGTT[A/T]CTGCAAAACTTAAAC	221687
rs541712229	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13966077	AAGAAAGGGCAATCT[A/G]TGTTTATACAAAAGA	221687
rs542059808	snp	A/G	3.29489e-05	0.00405874	synonymous-codon	RNF182	GRCh38.p7	6:13977233	ACCCAAAGTGCTGGA[A/G]TGTTGTCATAGGGTT	221687
rs542070628	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13942298	CTGTCTATCTTGCTT[A/G]GGGATCATAGAGGTT	221687
rs542070691	snp	G/T	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13950106	TTACAAAAAATACAT[G/T]CTACTTTTCTTACAT	221687
rs542130378	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962884	CAACTTACCCTAAGA[A/C]CTATACAATTAATTC	221687
rs542151938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936588	ACTGTGCTAGGCACT[A/G]ATGACTCAAAGATGA	221687
rs542361452	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13938693	CAGCGTTATTTATTG[A/G]AAATATTATCTCTTC	221687
rs542429713	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923246	TCTGTTCCTATATAT[A/C]CAGTTTTTTTGTACA	221687
rs542571225	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979005	AGGGGTGGGCAAGAG[A/G]CATGCAAAGCTGAAG	221687
rs542609662	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951172	ACACATATAAATACA[C/T]GGAGAGATGGAAGAA	221687
rs542697819	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979534	ACATGGGATATGGTC[C/G/T]AATGAATTTAAGCCC	221687
rs542699139	snp	C/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978585	CTCTCCTCAGTCTTA[C/T]CTGAGAAGAATGGAG	221687
rs542824862	snp	A/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924790	TGGTGGTGGCGGCCC[A/T]TCGGGGGTCCTTGTC	221687
rs542841182	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13950819	TATTTTTTTTGAGAT[-/A]AGAGTCTTGTTCTGT	221687
rs542874509	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943875	ACTAAAAGACATTAA[C/G]GGTGATTTGTATGTG	221687
rs542887368	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13976390	GGTAAGAACAGTCTG[C/T]TCTACTTAAATATGC	221687
rs542910141	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951973	CTTGCCCCTTTTGGC[C/T]CCTGCCTGTCATCTT	221687
rs543016054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928967	ACTTTATGGTCCAGA[C/T]TCTAAAGCAGATTAC	221687
rs543061857	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925401	TGGACTTTCATGTTT[A/C]ATGGCATTCTCTTTG	221687
rs543113214	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13965018	TAACAAAGAAAAATA[C/T]TGGCACTGTAGCCAA	221687
rs543151609	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964541	TCTCTCAATTCTACT[C/T]TATCTGCCTTTCCTG	221687
rs543201374	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951417	CCATCCCCTATGGGA[C/G]TCTTATCTCTCAGTT	221687
rs543231299	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13948380	TTTGGCCCCTTGTGG[C/T]ACACAATAATTTAAG	221687
rs543352205	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940772	AGTATGCTCTTAAAT[G/T]CTGTCACATTTTTTC	221687
rs543374657	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943581	TATTTTGCATACATG[C/T]CTGTCCCCCTCTGTG	221687
rs543378113	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925959	AGATTTAAATTGTGA[C/T]TGTGAAGACTTTTTT	221687
rs543432671	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13961567	CTAAATATAGGGTGC[A/G]GAGTACCTGGTTTTT	221687
rs543448342	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13948981	CTATTAATGTCAAAT[-/C]CAATTTTTAATAAAA	221687
rs543471402	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968275	ATGCAAAGACGATAA[C/T]AGAATTTGCGGAACT	221687
rs543583653	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13955442	TCTTGTGTCTTTCCC[A/T]TGGTTATTTGGTTTC	221687
rs543725281	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973376	ACTGTTGGGAGGGCA[C/T]GATTGGTTTTGAGAT	221687
rs543728222	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975902	ATTAAAAATAATTTT[A/G]AGATTTTGTATATTA	221687
rs543743863	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922452	TTTTTTAAAGTTATT[A/G]TTCCAAGTCTTTGAA	221687
rs543808333	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13933770	TGCCTGTAATCCCAG[A/C/T]GCTTTGGAAGGCTGA	221687
rs543841845	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13948751	ACTGTAAGTCATTTA[G/T]TTAGCCAAAATGACA	221687
rs544203076	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13941204	TTTTTCTACCTTTCA[G/T]TCTGTCAGTTTTTAA	221687
rs544253325	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971959	TAAAAGCATTCAGTT[C/T]TATGTATTCACAAAG	221687
rs544264613	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969863	TATATTTGAAAATGT[A/G]TGTATTTTTCTAGGA	221687
rs544348113	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13935669	CACTGAAATTGTTGA[A/C]ATTGTTATGATCTCT	221687
rs544383166	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13954568	TTAAATTAAATTAAA[-/T]TTTTTTTTTTAGCTC	221687
rs544392478	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963552	GTCCCTGGTGGTTAG[C/T]TGAGGCTGGATGGTC	221687
rs544420826	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936755	AGATTTGGGATTTGG[A/G]AATAATTGATGTCTA	221687
rs544459063	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13956497	ACCCAGCTAATTTTT[A/G]TATTTTCAGCAGAGA	221687
rs544542722	snp	A/G/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13930030	TTATTATTCGTATTC[A/G/T]TATATTAAAAGAATA	221687
rs544569546	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931831	ATATGTTGAAATTCT[A/G]ACTCCCAAGGTGATG	221687
rs544606319	snp	A/G	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13938743	ATTCTTTTCATAAAA[A/G]TAAGTAATCATATGC	221687
rs544664758	snp	G/T	1.64781e-05	0.00287033	missense	RNF182	GRCh38.p7	6:13977774	GTCTTTGTCAGCCTG[G/T]TCCCTTCGAGCCTCG	221687
rs544767651	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	RNF182	GRCh38.p7	6:13924406	GAGAGGAGGAGGAGG[C/G]GGAGAGGGAGGAGGC	221687
rs544794467	snp	A/C	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13960499	ACAAACAAACACAAA[A/C]AAAAAACCAAACCCA	221687
rs544801228	snp	A/G	0.0158469	0.0875917	intron-variant	RNF182	GRCh38.p7	6:13927899	GATTTGTGGCTGGGG[A/G]GAATAGTGTGGCCCT	221687
rs545074598	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13951033	AACACCTGGCCTCAG[A/G]TGATCTGCCCACCTC	221687
rs545087554	snp	A/G	0.00597247	0.0543191	intron-variant	RNF182	GRCh38.p7	6:13931719	AATACTGCCTCTGCC[A/G]CCTTTTAGTGATACG	221687
rs545100400	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13973242	CATTATATCTGGGAA[G/T]TAACTAACTTGCTTT	221687
rs545115339	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923563	GTGCATTTTGAATTC[C/T]GGCAGGTATTGCCAA	221687
rs545171601	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13945280	TTTAGCCAAAAATTA[C/T]TGTGGCCCACTTTAG	221687
rs545183670	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979334	CATTACTAATGATTA[A/G]CATTAAAATATTTGT	221687
rs545253611	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952463	ACTGAGAGGACCCTC[G/T]AACCCCTTACGTCTC	221687
rs545332874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938218	GAGACGGGGTTTCAC[C/T]GTGATAGCCAGGATG	221687
rs545354097	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954067	AGAAAATGATATAAT[A/G]AATCCCTTTTTACTT	221687
rs545408751	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957826	AGCCTTAAGGACAAA[C/G]TATACTTCTTCAGGT	221687
rs545410512	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13965996	TACTTTTTTTTGAGT[A/G]GACTGGAAGTACTCT	221687
rs545416160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945163	GTCTTTAGCCATCAA[A/G]CCCAGAATCTTAATT	221687
rs545523061	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13929464	ATAAAAGGTTTCTGT[A/G]TGGTCTTCTCTGGCC	221687
rs545558905	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13944691	GGTGTGCTATATCTG[C/T]TATTTGTACTTAATC	221687
rs545564023	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13931761	GCTGCTTAATCTCTC[C/T]GTGCCTTCATTTCGT	221687
rs545573415	in-del	-/C	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937769	TGGTTATATCGGCGA[-/C]ATTCTCAACATCAGT	221687
rs545578338	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13958057	TATAAGTCTTTTATG[-/T]TTTTTTTTAATGTTT	221687
rs545659433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941358	TCTTATAGTAGTATA[C/T]ACCAACTCTCCTTTG	221687
rs545733641	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13935140	GATGTACATGGAAGA[C/T]GCAAGGGGGCAAGAT	221687
rs545769804	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960716	GCACATGCATGTGAT[A/G]TACAGTATTAGTTAC	221687
rs545805274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953845	ATTTCTTGAAGGTGA[A/G]GCCATCGCCAGCACC	221687
rs545805614	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954949	CAACTGCTGCCTTGT[C/T]CCTCCCTTTGTTGTG	221687
rs545853772	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947279	TCAAAAACAATGGAT[A/G]AGACTAGAGTCTGGT	221687
rs545866742	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955575	CTGGACTTAGGCCCT[A/G]TGGGTACACAGGAGG	221687
rs545997417	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949333	AATCTTTAATAGAGT[G/T]GCCCCCTTGCTTCCA	221687
rs546036092	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956274	CTTCTGCTGCACACT[G/T]TCTCTGCTTTGGCCT	221687
rs546142648	in-del	-/TAAT	0.0103295	0.0711199	intron-variant	RNF182	GRCh38.p7	6:13968192	AATAGTTTGATTAGG[-/TAAT]TAATAAGGAGTAAAA	221687
rs546143755	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978208	CTCCTTTCGTATTCA[A/T]GGATGTTCTATGATG	221687
rs546262291	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936861	ATAAAGAGGGAACAG[G/T]GCATCATAAAAGCTT	221687
rs546291819	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13930023	CCTTAATTTATTATT[C/T]GTATTCATATATTAA	221687
rs546383719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940583	TTTTTTTGCTATTGT[A/G]TGCTTATTTTCTAAT	221687
rs546399342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970828	AGTTGATCCAAAATA[C/T]GCGTTGGCAGAAAAA	221687
rs546416168	snp	C/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13975970	CTGTGCATATGAAAT[C/T]AACCTTCAACCATTT	221687
rs546425436	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933810	GTCACCTGAGGTCGG[C/T]AGTTCGAGACCAACC	221687
rs546517392	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13935348	AATCCCTGTGTTGTA[C/G/T]TCCCAGATGTAGTCC	221687
rs546517519	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13969327	GAGCTTTGAGAAGTC[C/T]GGTTTGGGTCACATG	221687
rs546546339	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13926105	TTAAATCATATTTAA[A/G]CAATATGAGATGTCA	221687
rs546552745	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957959	ACAAATATTTATCAA[C/T]TGGAGATTTTAAATG	221687
rs546554192	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13938473	GAACTCATTTATACA[A/T]CTTCTTTTAATGTTA	221687
rs546594861	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13927349	ATGGTTTAGCCACCT[A/G]GTGGAAGCAGGCAAC	221687
rs546601239	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928303	GAGTATGGTTTTGGA[C/T]ATCAGTCATCAAATG	221687
rs546634731	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957714	TACCTTTGTGGCTTT[A/G]ACTGTATTTGTAATT	221687
rs546696212	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923475	AATGCATATCCTTTT[A/G]TATCTATCATTACAC	221687
rs546804701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934930	GCAGAGAGAGAAGAC[A/G]GGAGAGTCAGATGAA	221687
rs546825059	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956630	GCTCCCGGCCTGTCC[G/T]TTGCGTTAGACTACT	221687
rs546827056	snp	A/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13949123	CCTTTGCCAGTGCAG[A/T]GAGAGCAGCTTCAGG	221687
rs546834780	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13927457	TTTAGCTTACGGGTT[G/T]TAATTTTATGACGTA	221687
rs546843400	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13955812	AATTGCAGCACTTTG[C/G]GAGGTTGAGGTGGGA	221687
rs546923766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957505	CATTTCATTAATTGG[A/G]TTGGTGACATTTTTG	221687
rs547020002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969978	TGTTCTTATCAAGGC[A/G]TGCTACAGATATGTC	221687
rs547060505	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952760	TGAAAGCAAGTTCAT[G/T]AAGAAAGTAAGGGAA	221687
rs547124861	snp	A/G	0.00755907	0.0610114	intron-variant	RNF182	GRCh38.p7	6:13966826	GTTTTGTGTGTGTGC[A/G]CGTGCGTGTGTGTGT	221687
rs547176039	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13964014	GAAGAAGACCCAAAA[A/T]CAGTTCAAGATCCAA	221687
rs547226656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945671	TTTGTGTTAAGACCT[A/G]TTAGTTTATGCTATT	221687
rs547231167	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942585	GTCCTCAACTGATCT[A/G]CTTGCCTCAGCCTAC	221687
rs547253892	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13930605	GAAGAATGATTAAGC[A/T]TTTTAATTTCAGGAG	221687
rs547274583	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965534	ATTGGAAAAGTTCTT[A/G]AACTATATATTAAGA	221687
rs547412523	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959301	TTAACAAAGGCCAGG[A/G]CGGCAGGAAAACAAT	221687
rs547440738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960620	CAGCCATGGCTTTGG[A/G]AGTAATATGTACTTT	221687
rs547659782	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931534	GAATTCCTGGTGCAT[A/G]CTTTCCTTGATAACT	221687
rs547726680	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936410	CTCAGGATAATATCT[C/T]TACTGAGATTCAATT	221687
rs547730053	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922689	CAGTTTAGCTAAACA[A/G]ACTAAAAGCTGCCAC	221687
rs547763572	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13944072	CCTCCTACAAGAAGA[A/C]CTGGGCAACAGGAGA	221687
rs547771758	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13939335	GTCTTCTAATCAATG[A/C]ACACAATATAGCTCT	221687
rs547811678	snp	A/G	0.0158469	0.0875917	intron-variant	RNF182	GRCh38.p7	6:13952179	CGAGGAGCTCAGGGA[A/G]ACCAGGGAAAGACCC	221687
rs547868724	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944749	TGTCTCTATGTTACA[A/G]TCAAGAGACAGAAGC	221687
rs547877218	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13958910	AATGCTCTTCTTTGG[A/G]GGTGAATGAATTCTT	221687
rs547938710	snp	C/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923974	GAGGGATGACTCACT[C/G]CCCCCATGGAGGCTG	221687
rs547940165	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934619	CATAGGTAGTTTGCC[A/C]TTTAGATAGGATTAT	221687
rs548051622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966236	TGACAAAGATACTCA[A/G]TAATACAAAGAAAAA	221687
rs548075798	in-del	-/AGATAGTAAAGAGACAGG	0.00597247	0.0543191	intron-variant	RNF182	GRCh38.p7	6:13952090	CCTGCAAGACAGAAA[-/AGATAGTAAAGAGACAGG]AGAGAGAGAGAGGAA	221687
rs548088919	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974586	AGGTTCACATAATTA[A/T]CAGCTAGAAATTGTG	221687
rs548113301	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931901	GAGGGTGGAGCCCTC[A/G]TAAATAGTATTAGTG	221687
rs548129396	snp	C/T	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13974084	GATTTTTGGTTATTA[C/T]TCAAGTTCTTTGAGG	221687
rs548153618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963107	CCTTACTGTAGTAGA[A/G]CTTATGCAGTGTTTC	221687
rs548203184	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949030	CTCACTCCTAATCAG[G/T]TTGACCATAAAGTAA	221687
rs548207330	snp	A/C	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13940965	TTTTTTTTTGAGACT[A/C]TTCTTATGGCCTGGA	221687
rs548237824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928128	TTTTTCATGTTTTCA[A/G]TTAAAATGGAGATAA	221687
rs548239818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948586	TATGCCATTATTGGA[C/T]TTCAGGGGACCTAAT	221687
rs548309286	snp	A/G	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13966832	TGTGTGTGCGCGTGC[A/G]TGTGTGTGTGTGTGT	221687
rs548349670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13927452	TGCATTTTAGCTTAC[A/G]GGTTTTAATTTTATG	221687
rs548408588	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935642	AGCACATTAGTTATA[A/C]CCACAGGATGTCACT	221687
rs548450411	snp	A/G	0.000399281	0.0141238	missense	RNF182	GRCh38.p7	6:13977552	AGCTCCCCGTCCCTG[A/G]GCTCCACTCCTGTGG	221687
rs548510196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970048	TATAATAATTTACAT[A/G]TTTATGGGGTACATG	221687
rs548543793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961795	GGGAGGTAAGAGTTT[C/T]AATTGTTGAGGGAGG	221687
rs548582671	snp	C/T	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13940253	ATTTTCCGCATTTAT[C/T]GAGATGATGATATGA	221687
rs548586897	snp	A/G	0.00398564	0.0444627	utr-variant-5-prime, upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924922	CCCGCCCGCCAGCCC[A/G]CTAGCTCCTCGCGCG	221687
rs548605075	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965069	ACAGACAGAACTCAC[A/G]CTGAATGTGATGGAG	221687
rs548610073	snp	A/C	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13971955	CTGTTAAAAGCATTC[A/C]GTTTTATGTATTCAC	221687
rs548745516	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925637	CTAGCAAGACCAGAA[A/T]GTAGAGCAGTACCGA	221687
rs548749166	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979827	ATGTCTACAGTGATA[A/C]ACTTGTGTCTCCGTG	221687
rs548796594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966042	CAGATAAAACAAATA[C/T]AAGTTTTAAGCTTTA	221687
rs548834559	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955069	CCATTGATAATTATT[G/T]TGTAGGTTAGGGGTC	221687
rs548869280	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962280	CTCAAGCTCCATAAA[A/T]AATGAGGTTAGGAAC	221687
rs548896318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959005	TTCCTATCTTGCCAT[A/G]TGATCTCTGCAGATA	221687
rs548947306	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973951	GCTTTCACTGAACAT[C/T]ATGATTGTTGTCCAC	221687
rs549060798	snp	A/G	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13944275	TGGCTAGAACCAACA[A/G]TAAGTTATTTTGGCT	221687
rs549065944	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971084	ACTAAGTCTGCTTGG[A/G]CACTGTTTTTTCTTC	221687
rs549122287	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13949068	ACAAACCTTTTATAA[A/C]CCTTTAAATTTTTTG	221687
rs549151934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951715	CCTTTCTCTGAGTGG[C/T]TCTGATAGTCTTGCT	221687
rs549163007	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943190	TCATCCAAATAAAAA[A/C]TATTTAATAACATAT	221687
rs549179863	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13957284	TGCCACATTATGTGG[C/T]TGTGTTGCAAAGTGA	221687
rs549188548	snp	A/C	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13958165	GGCCGAGGCAGGCAG[A/C]TCACGAGGTCAAGAG	221687
rs549199903	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942697	TTTCTTCTGGTCTGA[A/T]CACTTTCCTCTGCTC	221687
rs549202645	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13939850	GCCCGGGCATAAATG[C/T]ATTTTTGTATCTTGA	221687
rs549232599	snp	C/G	1.69163e-05	0.00290824	utr-variant-3-prime	RNF182	GRCh38.p7	6:13977864	GCACCTCCTTCTTAA[C/G]TGATATGCAAAATAA	221687
rs549271370	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF182	GRCh38.p7	6:13980132	TGCCTTTATCATGCC[C/T]GTGAAGACTTCAGAA	221687
rs549354255	in-del	-/TCC	0.474723	0.109542	intron-variant	RNF182	GRCh38.p7	6:13930134	ATATTTGGAAAATAT[-/TCC]AAAAAATAATTCAAA	221687
rs549542538	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940281	TGATTTGTTCCTCCT[C/T]TATTTTGTCAATATG	221687
rs549567430	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13946795	AAATTTATCTTCTGT[A/G]GCTTCTTCAGGCTGA	221687
rs549575612	in-del	-/CT	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13951812	ACCCATAGGCAAAGA[-/CT]CTCAGTTTTGCAAGA	221687
rs549579335	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939745	AGATGGGGTTTCACC[C/T]TGTTAGCCAGGATGA	221687
rs549613460	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937093	TATAGACTTTTCACA[A/C]TCACATTACTTGTTT	221687
rs549793145	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13970451	CATTCTTTGTTATTG[A/C]CAAATAGTAGTTCAC	221687
rs549803747	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13953986	GGAAAGTAGAGAGAA[A/G]GCTTTGCTAATGATT	221687
rs549830948	snp	A/G	0.031825	0.122064	intron-variant	RNF182	GRCh38.p7	6:13960691	TGTGTGTGTGTGTGT[A/G]TGCGCGCGTGCACAT	221687
rs549965275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947545	TGTTCTATAATCTAA[C/T]CTTAGATTAGACTTT	221687
rs550428636	snp	A/G	1.64776e-05	0.00287028	missense	RNF182	GRCh38.p7	6:13977577	CTGTGGTAGAATTTT[A/G]TAGGCCTGCGAGTTT	221687
rs550457956	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975180	GTGGTGACCAGGATA[A/G]AACTCCTTCTTGTTC	221687
rs550463860	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960091	TGGAACCTGTGAGAA[C/G/T]AGATAGTTTCAAGAG	221687
rs550498868	snp	C/T	0.0103295	0.0711199	intron-variant	RNF182	GRCh38.p7	6:13966835	GTGTGCGCGTGCGTG[C/T]GTGTGTGTGTGTGTG	221687
rs550499464	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924689	GCGAATACCACTTGG[A/C]CCTGGGCTCGCTCCG	221687
rs550563211	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13934413	GTCGCTCACAGTTAC[A/G]TTAGTTGTTTTAATG	221687
rs550572159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942392	TGTGGCCCAGGCTGG[A/G]GTCAAGTGGTGTGAT	221687
rs550608960	snp	C/T	0.00358779	0.0422022	intron-variant	RNF182	GRCh38.p7	6:13941586	CTATTTGTTTTCTAA[C/T]TGTCCTATCTGTTCT	221687
rs550626297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962298	TGAGGTTAGGAACAT[C/T]GGGTTTTGTGAATGA	221687
rs550637492	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978158	GACAGACGGCAGGGG[C/T]GTGGTGTGTTATACT	221687
rs550672796	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13948854	CTTTTCTCTCCTTTC[-/T]TTTTTTTTTCTTTAG	221687
rs550733666	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936111	TCCTGAGAATTCTGT[C/T]GCGAGATAGCACTAT	221687
rs550790436	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970750	TTAAGGTGATAGATA[A/C/T]GTGACATTTCAATTT	221687
rs550847396	snp	A/C			upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924634	TGCGACGGGAGTTGG[A/C]ATGTCCAGTGTGGGG	221687
rs550859810	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964565	TTTCCTGATCCCAAC[A/G]ACTCCTGGAGCCAGC	221687
rs550859909	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956844	AATTCATCATTTCCT[G/T]GGCTGATATGAAAGG	221687
rs550883311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948619	CTAAAAGGATTATCA[A/G]GTCAGGAAAGACTTA	221687
rs550885987	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13927112	ATACAGAAATCAACA[A/G]TCATGTATTGCATGC	221687
rs550915834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926546	TGTTTTTAAACTGAA[C/T]TTTACCTGTGGAAGA	221687
rs550932553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956395	AATGGTGTGATCTAC[A/G]CTCACTGCAACCTCC	221687
rs550960200	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952460	CTTACTGAGAGGACC[C/T]TCTAACCCCTTACGT	221687
rs550963698	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931421	TTTCCTTGTTTTAGG[A/T]TGCCGAAGGTCTGGA	221687
rs551010823	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13965541	AAGTTCTTGAACTAT[A/G]TATTAAGAATAAGAG	221687
rs551026930	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959117	AGCCAGCCAGAATTC[A/T]GAATCAAATAAACCT	221687
rs551211257	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13949076	TTTATAACCCTTTAA[A/G]TTTTTTGTTGATGGC	221687
rs551298992	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932867	CTCATCTCTATATTT[A/G]ATTCTAAACCTTCTC	221687
rs551341259	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13945452	CCCTCAGAGCCCGTT[C/T]AGATGATTTTGCAGA	221687
rs551539180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937761	TGTCCAGGTGGTTAT[A/G]TCGGCGACATTCTCA	221687
rs551679588	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956071	GCCTGGCTTCTTTCA[C/T]TTCACATAATGTCGT	221687
rs551701025	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943933	GGTGTTTATCTGGAG[A/G]AGAAACAAACTTCTT	221687
rs551824642	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957371	TAAATTCAATAAAAT[G/T]TAATCTATAGTTCTT	221687
rs551932973	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934514	TTTTCTGAGTGACTT[C/T]TCCAACAATGTTTTT	221687
rs551973955	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934089	TGTATTTGCAGGAAA[A/G]GTATTTTTCATTGTT	221687
rs552008893	in-del	-/TTGTTGTTGTTG	0.00318978	0.0398085	intron-variant	RNF182	GRCh38.p7	6:13969106	GCTTGTCTCTGTTTT[-/TTGTTGTTGTTG]TTGTTGTTGTTGTTG	221687
rs552038772	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13972775	ATGGAAATGCCTGGA[C/T]GTCCAGGCAGAAGTT	221687
rs552115591	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979906	TTTGTATGACACCAG[A/G]AAACTCTTCATGCTA	221687
rs552173082	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969427	CACACCTTTGGAGAG[A/T]AGGGAGGTACTATGA	221687
rs552247368	snp	C/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13937648	CTTATACATGTGTAT[C/G]TGAGCATTTCTGTTG	221687
rs552367234	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975227	AAGATGTTCATCCCA[C/G]AGGAGGAAAAAAAAT	221687
rs552514660	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RNF182	GRCh38.p7	6:13976957	AGACAGAGTTATATG[C/T]AGAAGTTGAAAATGC	221687
rs552543708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967714	ATTTAAGAAAAGTAT[A/G]TAACCTTTTTAAAAT	221687
rs552585740	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932107	ATAAGCCATTCAGCA[C/T]ATGGTATTTTGTTAG	221687
rs552672837	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13963686	GGTCTCAGAATTCCA[A/G]GAGAGCAAGAGCAGA	221687
rs552690872	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961702	ATAACTTAGATTGCT[A/G]GGTTATTAACTTGGC	221687
rs552717715	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930975	CTTTCTGCTGCAGTG[A/G]AGATGCTTTTGGGAT	221687
rs552747940	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RNF182	GRCh38.p7	6:13924021	TTAGAGGAAGCATGA[C/T]CAAGGGTCTGCTGGT	221687
rs552776484	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963927	GGGCTAGGGCAAAGA[G/T]TATTTAGGGGAGATG	221687
rs552847185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968497	ACTTTTAAAGAACAC[A/G]TAATTTTATCAGTAT	221687
rs552878747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961633	CTGCTGGCAAACAGC[A/G]CAGCATAAATCACAA	221687
rs552891806	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13970226	CCCTAGTATGCTATC[A/G]AATATTAGAATTATT	221687
rs553023256	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948710	AGGTGTAAAACACTT[A/T]ATGTTATAAAATAGA	221687
rs553053437	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963373	GGAAAGAAATAGCAT[A/G]CTATTTTGCTTATCT	221687
rs553085604	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956370	GCTCCCATCATCCAG[A/G]CTGGAGTGCAATGGT	221687
rs553138090	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13953851	TGAAGGTGAGGCCAT[C/T]GCCAGCACCTAGCCC	221687
rs553214154	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13946119	ACTTTGGAAAGAATC[A/T]GTATTATCTTTAAAG	221687
rs553216218	snp	A/G	0.0126979	0.078662	intron-variant	RNF182	GRCh38.p7	6:13942100	TTGTCAGTTTCTTTC[A/G]GTACTTTAAAGATGT	221687
rs553248925	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13956941	ACACACACACCCAGG[A/G]CAGTACTAATCCCTT	221687
rs553249043	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949337	TTTAATAGAGTGGCC[A/C]CCTTGCTTCCAAGTG	221687
rs553301968	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13969984	TATCAAGGCATGCTA[C/T]AGATATGTCCATCCT	221687
rs553310286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949935	AATTTTAGTCAATTT[A/G]TTCACACACAGAATT	221687
rs553385873	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969724	CATTTGCCCAATAGT[C/T]CAGGAGCTCAAGCTA	221687
rs553397142	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951875	ATGAACATTTTCCAT[G/T]TTGTCCAGAGCAAAA	221687
rs553414884	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956637	GCCTGTCCTTTGCGT[C/T]AGACTACTCTATAAT	221687
rs553460627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944502	AAAGAGGACTCAGAG[A/G]AGCCTGACTAAAGTT	221687
rs553461724	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959125	AGAATTCTGAATCAA[A/G]TAAACCTCTTTTCTT	221687
rs553632625	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974879	GACTTCACATACCTC[A/T]GTCCTTTCTATGGCA	221687
rs553662369	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13927064	TTGGCTTCTTCAGAG[C/G]TGCATCATTTTCTGC	221687
rs553721901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938548	TCATGAAGATATTCT[C/T]CTATGCTACCAAGAA	221687
rs553749012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928852	GTGGCCAAAGGTGGT[A/G]CAGGGGTGGGGGTGC	221687
rs553802953	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13938087	CTCACTGCAAACTCC[A/G]CCTACCGGGTTCACG	221687
rs553875287	snp	A/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13937192	GGTTAACATACATAT[A/T]GAAAAGTGCACGAAT	221687
rs553930645	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13939271	TTTGATTGGAATTGC[A/G]TTGACTGTGTAGATC	221687
rs553994480	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13932327	TAGGCCTTTAAGTTC[A/G]ACTTGCATATGTTAA	221687
rs554018761	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13931721	TACTGCCTCTGCCAC[C/G]TTTTAGTGATACGAC	221687
rs554075276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965856	ACCGAGGGCTTATAT[A/G]GCAGGGCAGAAATGT	221687
rs554153125	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13958335	AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	221687
rs554271296	snp	C/G	0.00119737	0.0244387	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974324	GATGAAGGCTTTCCT[C/G]CTGATGGAATAGGTT	221687
rs554299125	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13964918	CACTGCTAGATCACA[C/G]GAGAAGAGACCATTG	221687
rs554301586	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13972176	TGGGCATGGTGGAAC[A/G]CGCCTGTAGTCTCAG	221687
rs554338374	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979456	GAATAGCAGTTTGAT[G/T]TTAATTGTAAAACTA	221687
rs554468684	snp	C/T	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13957648	GGAAAGTGAGCAAAA[C/T]GTTTTGGTTTGTGAC	221687
rs554474822	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936862	TAAAGAGGGAACAGG[A/G]CATCATAAAAGCTTA	221687
rs554479190	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13966148	AGACAGCAGCCAGAA[A/C]ATCCCATACATTTCC	221687
rs554482202	in-del	-/CCTCCCTA	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13956444	ATTCTCCTGCCTCAG[-/CCTCCCTA]GTAGCTGGGATTACA	221687
rs554490145	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926674	AAAAGTATTTTCTCA[C/T]TTAAGCATGAACAGC	221687
rs554546496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934127	CTAAATTTAAATTAA[C/T]TGAAATTAAATATGA	221687
rs554611746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925886	GTTATAGGTACCTTT[C/T]TCAGTGGCCCCAACC	221687
rs554641389	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13940445	GAGAGATTGGTGTAA[A/G]TAGCTGAATAGTGCC	221687
rs554688223	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977021	CTGCCTTTTTGCATC[A/G]CTGCCAGATTTGGAT	221687
rs554710188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967011	CTGGCTAATTTTTGT[A/G]TGTTTTTGTAGAGAC	221687
rs554771537	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13960366	ACCTAACTTGGCCAG[G/T]TGCAATGGCTTATAT	221687
rs554815931	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955406	AAAGGAAGCTGCATA[C/T]AAAGAAAAGGCAGAA	221687
rs554986305	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13964061	ACAATCTCAGTTAAG[A/G]AAAACACGAATTTTT	221687
rs555029380	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961028	GTAAGGTACTAAGCA[A/G]AAACCTAGACTTATG	221687
rs555067194	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13953077	CATCAGGACATTTCC[C/T]GGGTCTGTTATTTAC	221687
rs555137637	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957537	TGAGTCCGAGTACGG[C/T]TGGACCTTGGTGAAC	221687
rs555137715	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968604	CACAAAAAAGTCTAG[A/C]GACCAATTTAATTTT	221687
rs555191016	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13953725	GGAAGGCATAGATGC[A/G]CCTTCTCTGCATTCC	221687
rs555228790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946223	CCAGGCTAGAGTGCA[A/G]TGGCACAATCTCAGC	221687
rs555302647	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13950989	TTTAGTAGAGACGGG[A/G]TGTCACCATGTTGGC	221687
rs555310454	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947104	ATTGTGGGAACCAAG[C/G]TGATATGGGGTCGCT	221687
rs555315195	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13937903	CCTAATAAGTGATAT[G/T]GAGCATTTTTTCATG	221687
rs555333580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949209	AGAATGCCTCTCTTA[C/T]TTCTGCATTGTCCAC	221687
rs555371170	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13965983	TCAGTTCTTTGATAC[-/T]TTTTTTTTGAGTGGA	221687
rs555395105	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941841	GCTCTTTTTGGAATC[A/G]TTGTATCAGTTTAAT	221687
rs555409799	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13950112	AAAATACATTCTACT[A/T]TTCTTACATACCTTG	221687
rs555446500	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13956988	TAGTAAATCACCTGT[C/T]CACTGTGTGACCGAA	221687
rs555589881	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13943651	ATTGTTAGTATCATT[A/G]TATGGCACCTAGAAC	221687
rs555618889	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971080	CTGCACTAAGTCTGC[G/T]TGGACACTGTTTTTT	221687
rs555634306	snp	A/C	0.0023933	0.0345097	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979548	CCAATGAATTTAAGC[A/C]CCAAGATACAGCTAA	221687
rs555655821	snp	G/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13970366	AGGTATTTGTCTTTC[G/T]GTGCCTGGCTTATTG	221687
rs555745718	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928512	CAGTTAATTTTGTAA[A/T]GTTTTTTTAAAAAGT	221687
rs555770883	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945124	GCTCTTAGTTATAGA[G/T]CCCTGTTATGTTGGA	221687
rs555791216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939347	ATGAACACAATATAG[C/T]TCTCCATTTAATTAT	221687
rs555803369	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962673	ATTGTCTCATCATCT[A/G]GAAAGCAGTGTTTAC	221687
rs555853392	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13928019	AAAAGGCACAGGAGA[C/G]ACATGGTCATGGTGA	221687
rs555888897	snp	A/G	3.29473e-05	0.00405864	synonymous-codon	RNF182	GRCh38.p7	6:13977743	ACTGGTGTCTAAGAA[A/G]GTCACCCTTGGGGTC	221687
rs555915778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933237	AGTTATGGGTTATAT[C/T]AAAAAGTAAGAATTG	221687
rs555941843	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935624	TTGATGATCCAAAAA[G/T]ATAGCACATTAGTTA	221687
rs555979027	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13934497	TCTATACCTTCGCCT[A/G]TTTTTCTGAGTGACT	221687
rs556052098	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967131	GCTGTGTACCACATC[G/T]CTGGCAGCTGTTTAT	221687
rs556099019	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932425	CAAATTGAACAGATT[G/T]GATTTCTTAAATTAT	221687
rs556143437	in-del	-/TATTT	0.00119737	0.0244387	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923339	TCTATGAATTTTATA[-/TATTT]TATTCTTATTAATGG	221687
rs556154931	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13952887	AAGATAACAAAGCAA[A/C]AAGTCGTAGGGAGAT	221687
rs556200338	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13961931	TGGCATTTGTTGAGC[A/C]TATTCTTTTTAGGAT	221687
rs556461980	snp	A/G	0.0799831	0.183287	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925131	GCGCCGGGCCGCCCA[A/G]GCGCGCCGAGGAGAG	221687
rs556545278	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971678	GGAAGTTTGGAATTT[C/T]CTAGAGACTTTGAAT	221687
rs556580204	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13959360	AGAGGCCAGATTATA[C/T]GGTACCTTGCTGTGT	221687
rs556717574	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922850	GAAAAATGAATGTCT[A/G]GAAGAATGTCTCACA	221687
rs556834796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966298	GACCTTGAGATACAG[A/G]AAGATGACAGGAGGG	221687
rs556849097	in-del	-/GTGGT	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13937753	CAAACAGTTGTCCAG[-/GTGGT]TATATCGGCGACATT	221687
rs556861185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938546	TATCATGAAGATATT[C/T]TCCTATGCTACCAAG	221687
rs556965686	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924222	CAGCTGAGATCCATA[C/T]TGCAGCCTGAAAGTT	221687
rs557001402	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950800	CCACACCTGCACTCC[C/T]CCTTTATTTTTTTTG	221687
rs557037977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961838	GCTCCTTATGCTGCC[A/G]AACAACCATTAGGGG	221687
rs557043314	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13969707	AGGGCTGTGAAAACA[A/G]TCATTTGCCCAATAG	221687
rs557165129	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978201	TGGATCCCTCCTTTC[A/G]TATTCATGGATGTTC	221687
rs557177885	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13953815	TTCCTTATGGGCTCC[C/G]CCTCTAGACTGTATA	221687
rs557232692	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955463	ATTTGGTTTCAGAGT[A/G]GGTTATGTTCCTCAC	221687
rs557248139	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13940857	GACATTTATTACTTA[A/T]TTTCCAACGGTTTAG	221687
rs557315067	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13976308	GACTGGTATTGAAAC[-/A]AAAAAATTGAAATGG	221687
rs557379181	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957579	TCATCTCATGAGATG[A/T]TGTAGCCATTTTTAT	221687
rs557389176	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954122	ACATATGGCCAATCT[C/T]GCTTCATTTATCTGC	221687
rs557395882	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13949942	GTCAATTTGTTCACA[C/T]ACAGAATTTCTTTTA	221687
rs557430016	in-del	-/GAA			intron-variant	RNF182	GRCh38.p7	6:13953526	GGGAACAGAGTGGAG[-/GAA]GAGTCCAGTGTTTTA	221687
rs557541177	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951850	CCAACAGGCTATGTG[C/G]GGGAAACAAATGAAC	221687
rs557558122	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948001	ATTTTGTTTACAGTA[A/G]TATATTATACTCAAT	221687
rs557720915	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935778	ATAAGACATCTTACT[A/G]TGATTCATTTGAGAT	221687
rs557783981	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936258	AAACCATATCAGTAA[C/G]GAACTAGCATCATAA	221687
rs557804599	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13975903	TTAAAAATAATTTTG[A/G]GATTTTGTATATTAC	221687
rs557858810	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942779	CTCCTAAACTCTTTT[C/T]CCTATTTTCCATTGT	221687
rs557893601	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949824	GTTTTAAAACTTAAA[A/C]AAAATTTTGCTGAAG	221687
rs557948047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928738	TGCTTCTGTATCTTA[C/T]AATCGGTTGAAGTGA	221687
rs557978702	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950104	TTTTACAAAAAATAC[A/G]TTCTACTTTTCTTAC	221687
rs558029031	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13973254	GAAGTAACTAACTTG[C/G]TTTTGATTTTACAGG	221687
rs558039405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938404	AGAATTCTTCCACAC[C/T]GTAGCTTGCTTTTAA	221687
rs558191672	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972032	GCGGCTGGGTGCAGT[A/G]GCTCATGCCTGTAAT	221687
rs558221193	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978521	GCTTCATGGCAGAAT[C/G]TGGCCATTTGTCCTT	221687
rs558302265	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939478	TTTTCACCTTGTAAT[G/T]TTTTGTTTCTTGTGT	221687
rs558312077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925788	AGCACCTCTGGAGGC[A/G]GGTAGCTGGGCGGTG	221687
rs558350720	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF182	GRCh38.p7	6:13925213	CCTCCGGGCACCACG[A/G]GGGCCGCCGTCCTGG	221687
rs558412069	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13951075	GTGCTGAGATTACAG[A/G]TGTGAGCCATTGTGC	221687
rs558426523	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13968033	ATAAAGACAAAGTGT[A/G]CTCTTAGTATGAATT	221687
rs558450098	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13970769	CATTTCAATTTTGTG[-/A]AAAAAAATTAATGGA	221687
rs558559101	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946979	GAAAACATTGAGTAA[A/G]CTTATCCTGAATTAT	221687
rs558612790	in-del	-/T	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13956453	CCTCAGCCTCCCTAG[-/T]AGCTGGGATTACAGA	221687
rs558639937	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974245	TGCATTTCCAGGGAT[A/G]CTACCAGAGCTCAAG	221687
rs558647761	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971437	TTTCTTTATAAATTA[C/T]TTAGTCTTGGGTATA	221687
rs558660607	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922955	GAGGGCAGGGATGGC[C/T]AAGTCAATGGTCCCT	221687
rs558677247	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975525	TCTATAGATTGACTT[A/C]TTTTTGCCACCAACT	221687
rs558718616	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13953349	CTAGTGAAGATGTAG[A/G]ACAAAGGGATTAGTA	221687
rs558801749	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961893	TTCTAGAGTCAGCTG[A/T]TGGTCCTTCAAGAAT	221687
rs558835490	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968761	ATGTCTGATGACCTT[C/T]GTGTATTTATATATG	221687
rs558902366	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13956914	CAAGCACCACCCCCC[C/G]CCCCCCACCATACAC	221687
rs559197253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13927390	ATCCCCAGGTGTAAA[A/G]TACTAGTCATCACTC	221687
rs559241502	snp	C/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13960227	TCTTGATTGTCTTTG[C/G]ATCCCCAGCATCTTG	221687
rs559358223	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13947624	GTTGGATAAGTTTCT[C/T]TCCTCTGGATGTCCC	221687
rs559360522	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935837	GAAATGGGCTATGCT[A/G]TTGATACAGTTTGAT	221687
rs559369020	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13939007	TGAATTGCTTGAACC[C/G]AGGAGGCAGAGGTTG	221687
rs559414850	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13976007	AGCTGGTAATAACCA[A/G]TAATAGTAATTAGTA	221687
rs559473114	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949002	TTTAATAAAATCATA[C/T]GGACAAAATCTACTC	221687
rs559488412	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13976555	TTTCTGTTTCTGATA[C/T]ATGTCCCATTCTGTT	221687
rs559511774	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13955597	CACAGGAGGAGCCCC[A/G]TGGCTGGTGTTGGTT	221687
rs559511816	snp	C/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13948541	TTGACAGTACTTCCT[C/G]TATGATTTTAGTATG	221687
rs559535980	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13939631	TCGCTGCAAGCCCTG[C/T]CTCCCAGGTTCATGC	221687
rs559562538	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928513	AGTTAATTTTGTAAT[A/G]TTTTTTTAAAAAGTT	221687
rs559607133	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13951225	TTATTTGCCAGTTTT[A/C]AGTTTCTTAACTGGA	221687
rs559607532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13935155	TGCAAGGGGGCAAGA[C/T]TGGTAGCAGGGAGAC	221687
rs559645805	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968540	AGAAGATGAATAGCT[C/T]GTGTTTCACTTATAA	221687
rs559654794	in-del	-/GCTGG	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13956455	TCAGCCTCCCTAGTA[-/GCTGG]GATTACAGATGCATG	221687
rs559717155	snp	C/T	9.88875e-05	0.00703093	missense	RNF182	GRCh38.p7	6:13977544	AGAGAGAGAGCTCCC[C/T]GTCCCTGAGCTCCAC	221687
rs559742242	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13947293	TGAGACTAGAGTCTG[G/T]TAACAGGTGTACCAT	221687
rs559764137	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943836	GGAGCCCTTTTAAAT[C/G]CTGGGATGTACTAAA	221687
rs559775648	in-del	-/T	0.0023933	0.0345097	downstream-variant-500B	RNF182	GRCh38.p7	6:13980198	AAAAGGCCTTCATAG[-/T]TTTTTTTATTTTATT	221687
rs559788611	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957892	AGAATTTTATTCTCT[A/G]AATTGTATTAATAGA	221687
rs559806653	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972477	GGAAAATGTCTCTGC[A/G]TATCAGAGGTCTTTA	221687
rs559810859	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF182	GRCh38.p7	6:13980433	AAATTTTAAAAATCA[C/T]ATGGCATCTAACTAT	221687
rs559858418	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13933816	TGAGGTCGGTAGTTC[A/G]AGACCAACCTGGCCA	221687
rs559869940	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13973527	AGATAATTGAATCAT[A/G]GAGTCAGTTTCCCCT	221687
rs559875580	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13951971	AACTTGCCCCTTTTG[G/T]CCCCTGCCTGTCATC	221687
rs559927825	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955622	TTGGTTAACAGTTGC[A/G]CAGCAACCACAGGGC	221687
rs559966416	snp	A/C	0.474723	0.109542	intron-variant	RNF182	GRCh38.p7	6:13930130	AAAAATATTTGGAAA[A/C]TATTCCAAAAAATAA	221687
rs559983584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926183	TTAGTAAAATAATGT[A/G]TAAGTTGGAATAGGT	221687
rs559989255	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962183	AAGCTCTAACTAGAA[C/G/T]CCAGCTTCTGAATCT	221687
rs560024175	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925555	ATTGAATCGAAAGAC[A/C]TTTTTTTCTTTGGAA	221687
rs560142175	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937048	TAAATGATCAGATTT[G/T]AGTTTTAGAAAGTCT	221687
rs560190202	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13943282	AGAGGTGGTTCCTGC[-/T]TTTTTTTTTTTTTCT	221687
rs560361364	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13958878	TGAAATTTGACTAGA[A/T]CTCTCATGAATAGAT	221687
rs560366951	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13977890	AATAAGAAATTGGAC[A/G]CACATTGCCCTGTTT	221687
rs560416853	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13950372	ATAAAAAATGTCATA[A/G]AAGCAGTTTATGACC	221687
rs560426147	in-del	-/TT	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937771	GTTATATCGGCGACA[-/TT]CTCAACATCAGTGTA	221687
rs560479299	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970621	TAGAAGAATTGCTGG[C/G]TTGTAAGGTATTTCT	221687
rs560557954	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13951430	GAGTCTTATCTCTCA[A/G]TTGGGGTGGGGACAT	221687
rs560563994	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924605	GTGGAGGGTGTCTGT[G/T]GGGGGGATGGTGGTG	221687
rs560564816	snp	C/T	0.00953873	0.0683987	intron-variant	RNF182	GRCh38.p7	6:13957225	AACACTGCAGGCTTT[C/T]ACTTTATCCTAATCT	221687
rs560586604	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971334	TTGCCTGTCACCACA[G/T]AAGATGTGCCTTTGC	221687
rs560593923	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13929059	GCTGGTCCTGGTCAC[-/T]TTGCCTCCATTTTTC	221687
rs560668087	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13961431	AGTGTCAGAGCCAGG[G/T]CCCAAATCTCGGTCT	221687
rs560704870	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13964231	GTGTCCAGTTTATGG[-/A]TTCTTAGAATGAGAC	221687
rs560737279	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13929968	TGTACATAGAAACTA[A/G]AATAATTTATGAAAA	221687
rs560738359	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979789	TCTGGACATGGGTAC[A/G]ATGTGTTTTGCTTCT	221687
rs560803995	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943162	ATAAAGTACTGTTAA[G/T]GTATACTTTTACTCA	221687
rs560818928	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967290	AAAGGCATAAATAGG[A/T]TAAGGAAAGACATTA	221687
rs560904570	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13949479	TGACGAGAAAGGCTG[G/T]TTATAAGAAAAAATT	221687
rs560960093	in-del	-/CAAC	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937775	TATCGGCGACATTCT[-/CAAC]ATCAGTGTATGAAAG	221687
rs560981430	snp	A/G	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13968225	ACAATTTAGAAGACT[A/G]TAAGTGAGAAAAGAA	221687
rs561136410	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13925900	TCTCAGTGGCCCCAA[C/G]CCTTGCAATCATTTC	221687
rs561309288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952198	AGGGAAAGACCCACC[C/T]AGTGCAGCAACACTG	221687
rs561312047	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931997	GCACCATCTGTGAAC[A/C]AATAAGTGGTCTTTG	221687
rs561330602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945279	ATTTAGCCAAAAATT[A/G]TTGTGGCCCACTTTA	221687
rs561351648	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938899	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC	221687
rs561355793	in-del	-/TG	0.00438332	0.0466095	intron-variant	RNF182	GRCh38.p7	6:13958438	GTCTACATTATAAAA[-/TG]TGTAGCATTCAAGAA	221687
rs561370505	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944788	TTTAAATAACATGTT[C/T]AGGGTCATATAGTCA	221687
rs561409389	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13933334	CAGCTTGGGCAACAT[A/T]GTGAGATCCCACCTC	221687
rs561521709	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13939565	TTTTTATTTTTTGAG[A/G]CAGAGTCTCTCTCTG	221687
rs561566714	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13956405	TCTACGCTCACTGCA[A/G]CCTCCACCTCCCAGA	221687
rs561579771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932747	CAGTTTGATGTCAGA[C/T]TCTTTTAAACGTTAA	221687
rs561603627	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974592	ACATAATTATCAGCT[A/G]GAAATTGTGGCTGGC	221687
rs561696437	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13931449	GGAGTGTGGTATCAG[A/G]GATGAAGTTAGAAGT	221687
rs561772116	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940758	AGCATGGCTTTAATA[G/T]TATGCTCTTAAATTC	221687
rs561787240	snp	C/G	0	0	intron-variant	RNF182	GRCh38.p7	6:13928987	AAGCAGATTACCTGA[C/G]GTCTTTACCTAGTGA	221687
rs561835855	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13969248	TTTCTGGTTCTGTAT[C/G]CCTTCCCCTGGTCCC	221687
rs561895189	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978150	CACTGCCAGACAGAC[A/G]GCAGGGGTGTGGTGT	221687
rs561897797	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13969832	GTTCATTGGTTAGTT[A/G]GGAATACCAGCTTCA	221687
rs561945244	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13935943	ATTGACTCACAGTTC[C/T]GCAGGCTGTACAGGA	221687
rs561993604	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934897	CATTTCAGACAGAAT[C/T]AGTGCAAAGGCCCTG	221687
rs562010158	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969886	TTCTAGGAAAAGAAA[A/G]CTTTGTATTTATTTT	221687
rs562101151	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934397	TGGATTCTTCATTTC[C/T]GTCGCTCACAGTTAC	221687
rs562135102	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13958215	ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA	221687
rs562174562	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938124	TCCTGCCTCGGTCTC[C/T]GCGTAACTGGGACTA	221687
rs562180475	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13926872	ATTCAAGTTCAAGGA[C/T]TTGGTCCGTGCTTTC	221687
rs562217540	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13929714	ATCACTTTCTGTTAC[A/G]TTAACCCAAAGGTAC	221687
rs562243387	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966089	TCTATGTTTATACAA[A/G]AGAATAGTCTATAGG	221687
rs562308253	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	RNF182	GRCh38.p7	6:13980492	TTGGGAATATGCAGC[A/C]GTTTTATGCTTATGA	221687
rs562336537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931382	TCAGGGTCAGAGCAA[C/T]ATGCTTTTTGCTACA	221687
rs562382970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955741	GCTTTATGATCCACC[A/G]TGGTACCATTTTTTA	221687
rs562398221	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922501	ACTTACTGAACATAC[C/G]AATTCAGTAGCTAAT	221687
rs562435700	in-del	-/CAG	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937781	CGACATTCTCAACAT[-/CAG]TGTATGAAAGTTCTA	221687
rs562456341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959834	TGTGTTAATACAAAT[A/G]GAGGTACTGTAAGCC	221687
rs562488945	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960723	CATGTGATGTACAGT[A/G]TTAGTTACATTTAGT	221687
rs562557943	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13931734	ACCTTTTAGTGATAC[A/G]ACCTTGAGGTAGCTG	221687
rs562592317	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974414	AGTATTTCCATTGCA[C/T]GTTACCAAGAAGTCC	221687
rs562617793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952591	TGGTGCTGTGCAGAC[A/G]ATTTTCCTTTGGTTA	221687
rs562718635	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923255	ATATATCCAGTTTTT[C/T]TGTACAGAATGGGAT	221687
rs562847956	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943887	TAAGGGTGATTTGTA[A/T]GTGTAGTTAGGCAGT	221687
rs562907974	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926961	TCTGAGTGCTGAAGA[A/G]CGGAGATATCCATGG	221687
rs562931997	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13966417	TGGAAAATTCACAAA[G/T]TTTTAGAATTCATTA	221687
rs562954675	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13964716	GTCCCACCAGAAGAT[A/C]AGGATGCACTGGATA	221687
rs563063878	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933834	ACCAACCTGGCCAAT[A/G]TGGTGAAACCCCGTC	221687
rs563103176	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935545	CACTCTGATTCTGAC[A/G]GTGGAATGACTTACA	221687
rs563198118	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13951976	GCCCCTTTTGGCCCC[A/T]GCCTGTCATCTTTGA	221687
rs563208686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941252	ATGTTATTGGATATA[C/T]ACAAACTTATAATTG	221687
rs563237814	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13961603	TCTTATTCCTGAACA[C/T]TTATTGGTTTAAAAC	221687
rs563251627	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13940864	ATTACTTAATTTCCA[A/G]CGGTTTAGGATATTC	221687
rs563437943	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948834	TTAGCTTTCCAAATA[A/G]TGTCTCTTTTCTCTC	221687
rs563479708	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938908	GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA	221687
rs563522248	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979379	GGGCATTACTAAGAC[A/G]ACTTTAACTTGTTAT	221687
rs563546870	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948408	AAGATAACAATTATA[A/C]CTATTAATGATAACA	221687
rs563574075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945404	AAACGTTGGAATTGC[C/T]CTTATGAGGAGATGA	221687
rs563683196	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13948402	TAATTTAAGATAACA[A/G]TTATAACTATTAATG	221687
rs563806635	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946296	CTCAGCCTCCTGAGC[A/G]GCTGGAACTACAGGC	221687
rs563866048	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13933771	GCCTGTAATCCCAGC[A/G]CTTTGGAAGGCTGAG	221687
rs563902780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940042	GCTCTATCTAGGACC[C/T]CAATTATAATTTTGA	221687
rs563902866	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13932832	CTTTTCTAAAAAGTA[A/G]TAATACAAGTCTGAT	221687
rs563944480	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978836	AACAATTCGAGGTGA[A/G]CTGTGGCAATGAAAA	221687
rs564034191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943037	TTTCTGAAATTCTTA[C/T]TTGGTAGATTAGTAG	221687
rs564127332	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13970119	GTAATTAGGGTATTC[A/G]TCACCTTAACTGTTT	221687
rs564164111	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13939023	AGGAGGCAGAGGTTG[C/T]AGTGAGCCAAGATTG	221687
rs564176254	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13973042	TACCCTACAGAGCCA[C/T]AGGGGCAGGGCTGTC	221687
rs564257399	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972435	CATAAGTAATGAGGA[C/G]CCAAATGTTAATTGC	221687
rs564299432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963558	GGTGGTTAGTTGAGG[C/T]TGGATGGTCTCTAAT	221687
rs564305037	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13929275	CAACATATTGTATTT[G/T]AGTGAGAAGTTGTGT	221687
rs564306845	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13937438	ACTTTATGTGTGTGT[G/T]TATGATAGCTTTCAC	221687
rs564471406	snp	A/G	3.29609e-05	0.00405948	synonymous-codon	RNF182	GRCh38.p7	6:13977416	AGGCAAAGGGAAGAA[A/G]TGCCTGCCAGAGAAC	221687
rs564534940	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923653	TTCATTCAGAATATT[A/C]CCATTACAAGAAAGT	221687
rs564557132	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978957	ATGATGGTTTAGGTT[C/T]ATGTGCAAGACTTTG	221687
rs564573484	snp	A/C	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13931839	AAATTCTAACTCCCA[A/C]GGTGATGGTATTAGG	221687
rs564595601	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924571	AGCTCCACAGGAGAA[A/C]GGTGTGGTGGTGGTA	221687
rs564635039	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959958	AATCCAAGGGAAAGA[G/T]TGCAAGCAAGGGCTA	221687
rs564696953	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13960513	ACAAAAAACCAAACC[C/T]AACTGTTACTCTTTT	221687
rs564743781	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943534	TACAACTTTGTACCA[C/T]TGGTACTTATCTTAC	221687
rs564787718	snp	C/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13949467	CTGGCCTTTGGTTGA[C/T]GAGAAAGGCTGGTTA	221687
rs564820148	snp	C/T	0.00795532	0.062565	intron-variant	RNF182	GRCh38.p7	6:13945724	TTTATTCCCTTGTTA[C/T]ATTCCATTACTGCTG	221687
rs564855582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953234	CTCAGCCCCTAGGCA[A/G]GAAGGAGTCACTCTA	221687
rs564901107	snp	A/C	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13932550	TATGTTTATTGGGCA[A/C]ATTTATGACTCAAGT	221687
rs564987756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967222	GCAAATGCGGAGTCA[A/G]TAGAACAAGTAATAT	221687
rs565015333	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13946596	TTATTAACTTCTTCC[C/G]TTAACTGTAAATATC	221687
rs565021703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975062	GGTACTGTTGTAAGA[A/G]CCTTGTGCTCAGCAG	221687
rs565197925	snp	C/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922727	ATTCAAATGATATCC[C/G]CTGGTAAGTAAGGTG	221687
rs565244462	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13965998	CTTTTTTTTGAGTGG[A/G]CTGGAAGTACTCTCC	221687
rs565383910	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944717	TAATCCTTTCAATAC[A/C]CCTGTGAGGTCAGTA	221687
rs565649529	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926641	AGTAGATCTGTTTTG[A/T]GAAGATAAACGGGAG	221687
rs565707157	snp	C/T	0.00478085	0.0486577	intron-variant	RNF182	GRCh38.p7	6:13974806	ACTGGCTGTTTTACT[C/T]TTTTTTTCTGATGTC	221687
rs565730113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937923	ATTTTTTCATGTTTT[A/G]TTAGCCATTTGGATA	221687
rs565739781	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13971192	TTCCCACATCAAGGG[G/T]GGAGCCAGGTGGAGA	221687
rs565754059	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934091	TATTTGCAGGAAAAG[C/T]ATTTTTCATTGTTTC	221687
rs565783797	snp	A/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13934523	TGACTTCTCCAACAA[A/T]GTTTTTTTGATTTGT	221687
rs565786947	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13944817	CAGTGATCAGTGGAG[A/T]TGGGATTCCAACCCA	221687
rs565828797	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13970024	TCCATTTTCCCTCTT[C/T]TGTTAATATATAATA	221687
rs565891484	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13976249	GGGTGTTATATGCCT[C/T]ATTCTTCCTTTAATG	221687
rs565901715	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13944325	GCTCTGAGCTTTCTC[A/G]GGTAGGCATGTTAAG	221687
rs565955606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13962533	TGATTCTCCATTTTG[C/T]ACAAAATAAATTGAA	221687
rs565994668	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13969494	AGTAGGAAACACTAC[C/T]CCGAAGAAGTGGGGG	221687
rs565995772	snp	C/T			downstream-variant-500B	RNF182	GRCh38.p7	6:13980181	CTAACCCATCACACT[C/T]TTAAAAGGCCTTCAT	221687
rs566071474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966908	GTGGTGCAATCATAG[C/T]TTACTGCAGCCTCGG	221687
rs566126140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13932170	AAAGTGGAGACAATA[A/G]TATTACTTCACTTGG	221687
rs566140945	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978270	GACACAAAGTGTGTA[C/T]TCCTTTCCCACCCCA	221687
rs566152576	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924832	CCCGGACTGCTGAGG[A/G]GAAGGGCCGGGGGGG	221687
rs566153965	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13949250	AGTCATATTCAGACA[C/G]CAGTTGTTTCCTCTG	221687
rs566158403	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967721	AAAAGTATATAACCT[C/T]TTTAAAATTTATTAA	221687
rs566204820	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949484	AGAAAGGCTGGTTAT[A/G]AGAAAAAATTACGGA	221687
rs566393315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953655	GCAAAGTAGACAATC[A/G]GGAGAGATTAGCCAT	221687
rs566479936	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13940007	TCTTGTATCTTACAC[-/T]TTTTTTTTATTGCCT	221687
rs566500219	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928501	TCAAAAGTTACCAGT[G/T]AATTTTGTAATGTTT	221687
rs566583036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13929365	GACATGGTGTTTTAC[A/G]TAATTTGATCACCAT	221687
rs566588663	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963994	TAATATCATGAAAAA[A/G]TGGGGAAGAAGACCC	221687
rs566640229	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956095	ATGTCGTTCAGACTT[A/G]TTCATATTGCTGCAG	221687
rs566683236	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13936187	CTACCACCAGGCCCC[A/G]CCTCCAACATTGGGA	221687
rs566748604	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943453	GATGGAGATATAAAA[A/G]TGGACTTTCTTTTTT	221687
rs566752743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13951676	ATTCCTACCTTTTTG[C/T]CAGCATGCCAGGTTT	221687
rs566921800	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959034	TATCGGCTCCCTTTC[A/G]TTTCTTCCCATGGAT	221687
rs566979297	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930734	ATTGTAATAACTACC[A/G]TTTATTAAGCATTTA	221687
rs567003782	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945684	CTATTAGTTTATGCT[A/G]TTTTTTGTGTTAAAC	221687
rs567018650	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936184	CACCTACCACCAGGC[C/T]CCGCCTCCAACATTG	221687
rs567204730	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960014	ATAGAAGAGGAGCTG[A/G]CAGAAAAGATTGAGA	221687
rs567274033	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13940317	CACATTTTAAAAAAA[-/T]GTTAGAACAGTTTTG	221687
rs567390987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939278	GGAATTGCATTGACT[A/G]TGTAGATCAGTTTGG	221687
rs567509071	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922704	GACTAAAAGCTGCCA[C/T]TTAACCTATTCAAAT	221687
rs567527428	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950132	TACATACCTTGCTCC[A/G]ATAGTCTCAATTACA	221687
rs567549298	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924653	TCCAGTGTGGGGAAG[C/T]AAAGGAGTGCCTACT	221687
rs567619774	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13930592	TACTGTCTCCATAGA[A/G]GAATGATTAAGCATT	221687
rs567654565	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937857	TAGCAGATGAAAAAT[G/T]ATATCTCATTGTAGT	221687
rs567851326	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13959302	TAACAAAGGCCAGGG[A/C]GGCAGGAAAACAATA	221687
rs567949031	snp	A/G	0.00755907	0.0610114	intron-variant	RNF182	GRCh38.p7	6:13966828	TTTGTGTGTGTGCGC[A/G]TGCGTGTGTGTGTGT	221687
rs568039472	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13930256	GATGTACATAGGTTA[-/T]TATGCAAATACTATG	221687
rs568075800	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13967746	TATTAATTTTTTTTT[A/T]AAAAATAGAGATGGA	221687
rs568087858	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13976167	AGAGACATAGCTATG[C/T]ATGTTTTATCTGTGT	221687
rs568105131	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940988	GGCCTGGATATGATC[A/G]TTTTTGCTGAGTGAT	221687
rs568126627	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975417	GTGTTAGGCTAGATA[A/C]ATAGAGCTTGGTTCG	221687
rs568153309	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934646	TTATGAAGACTGAAC[G/T]GTGATCCACGCATGA	221687
rs568167995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941551	TTGATAATATAATTG[A/G]GTTTAAACTTCCCAT	221687
rs568191704	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13927478	TTATGACGTAAAATT[C/G]GTCCTAATTTTTGGT	221687
rs568235206	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970095	AGAATGTATGATGGT[C/T]AAGTCAGGGTAATTA	221687
rs568305057	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13962043	GCATAGTAAAACCCT[C/T]AATTCTGAGACCATC	221687
rs568350173	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13963838	AAAAGAAGATCACAT[C/T]GTAGAAAGTATTTGT	221687
rs568388939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970726	TTGATTTATAGTAAT[A/G]CATGAATATTAAGGT	221687
rs568400890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963195	TTATTAAAGTTTATG[C/T]ATGGAAGAATACATA	221687
rs568404343	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13967620	AAGGAAAAGATTTTC[G/T]TATAGATTTTGTTCT	221687
rs568429746	in-del	-/A	0.00755907	0.0610114	intron-variant	RNF182	GRCh38.p7	6:13958074	TTTTTTAATGTTTAT[-/A]AGATTTCTTGGGAAG	221687
rs568469965	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF182	GRCh38.p7	6:13925102	GGCAGCAGCCAGCCC[C/G]GCAGTCCTGGACGGC	221687
rs568487322	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13961049	TAGACTTATGAGCTT[C/T]ATATATTATTTGTTG	221687
rs568529871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961821	GGAGGCTTTCTGGAA[C/T]TGCTCCTTATGCTGC	221687
rs568648898	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965426	AATATAAGAAACAAA[G/T]TTTTTGAGCTTAAAA	221687
rs568672585	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955124	AGATAGTAAATAGTT[C/T]TGGCTTTGAGGGCCA	221687
rs568723927	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13932586	AAACCTTACCAAATA[C/T]TTAGGTTAAGTTCCT	221687
rs568731002	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956014	AAAACTTTTTATTAG[C/T]TCCCACATATGAGTG	221687
rs568749943	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940500	AATCTGTGCCTTTTT[C/T]CCCCCCTTGATCAGT	221687
rs568808096	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13972626	GGCTAAAAGGGGTCA[A/G]TGTACAGCTCAGCCC	221687
rs568857308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13958205	ATCCTGTCCAACATG[A/G]TGAAACCCCGTCTCT	221687
rs568970552	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957561	GGTGAACAGAAATCT[C/G]CTTCATCTCATGAGA	221687
rs569109761	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13956761	CTTCAAGGATACCAA[C/T]GGCTGAGCTCTTTTT	221687
rs569117501	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13944843	ACCCAGATGTTTTTG[A/G/T]CTTCAAATGACTCTG	221687
rs569149351	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943214	AACATATATATCAAA[A/T]CCCTTGGTAAAAATA	221687
rs569149384	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13936214	GGGAATTACAATTCA[A/G]CATGAGATTTGGGTG	221687
rs569156111	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13952295	ACATTTCCCCCTTTG[C/T]GGGAGAGAAAGCTCC	221687
rs569196470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944283	ACCAACAGTAAGTTA[C/T]TTTGGCTTAAGAAAT	221687
rs569228859	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13964291	AATATGCAAAAAGGA[C/G]AATTCTAAAAAGTGA	221687
rs569271868	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13938956	GGTGTGGTGGTTCAC[A/G]CCTGTAATCCCAGCT	221687
rs569290711	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13961706	CTTAGATTGCTAGGT[A/T]ATTAACTTGGCTGTA	221687
rs569294648	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928103	AAAACTTTTGTGGAC[A/G]TGTGTTTCATTTTTC	221687
rs569310907	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13950591	CAACCTCCATCTCCC[A/G]GGTTCAACAATTCTC	221687
rs569394798	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13939760	TTGTTAGCCAGGATG[A/G]TCTTGATCTCCTGAC	221687
rs569412123	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978443	GGGTAGTTTCAACTG[A/G]ATACCAGTTTTGCCA	221687
rs569533071	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13937195	TAACATACATATAGA[A/C]AAGTGCACGAATCGT	221687
rs569533888	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13932030	CAGATACCTAATCTG[C/T]CAGCACCTTAATCTT	221687
rs569539461	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928574	TTTGGTTAATTTGTA[A/T]TTTGATCAGAAAATA	221687
rs569559327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933282	TCACACCTGGAGGCC[A/G]AAGCAGGAAGATCAC	221687
rs569569749	in-del	-/TTTATT			intron-variant	RNF182	GRCh38.p7	6:13939531	TTTTTTTATTTTGTA[-/TTTATT]TTTATTTTTATTTTT	221687
rs569596725	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953550	AGTGTTTTATATTCA[A/C]GAGTCATGGAATAGG	221687
rs569731714	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13968219	AGTAAAACAATTTAG[-/A]AGACTATAAGTGAGA	221687
rs569776471	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13972106	GAGATCAAGACCATC[C/G]TGGCTAACACGGTGA	221687
rs569777920	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13935270	TGATACCATCGTCAC[G/T]AGACTGTAAGCTCCA	221687
rs569940574	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940035	CCTCATTGCTCTATC[C/T]AGGACCTCAATTATA	221687
rs569975469	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13976200	ACTTCTCTTTCTTGG[A/G]ACTTAGACTTGACTT	221687
rs570022129	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922873	GTCTCACAGAATAAC[A/G]CAGGACCAGGTCACT	221687
rs570096792	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974232	TACTTGTGTTGGCTG[A/C]ATTTCCAGGGATGCT	221687
rs570110485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938381	CCTTTGTGCAATGTA[C/T]GTGTTACAGAATTCT	221687
rs570132835	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13932055	AATCTTGGACTTCCC[A/C]GTTCCCAGAACAGTG	221687
rs570167994	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13938960	TGGTGGTTCACGCCT[A/G]TAATCCCAGCTACTT	221687
rs570234059	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13974721	TGTTCTTACGTATTC[A/G]TAAACACTCACATGT	221687
rs570235034	snp	A/G	0.0325976	0.123435	intron-variant	RNF182	GRCh38.p7	6:13966836	TGTGCGCGTGCGTGT[A/G]TGTGTGTGTGTGTGT	221687
rs570325600	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965606	ACTTACCATGAAGAA[A/G]TATCACACTAGCAGC	221687
rs570360477	snp	C/T	0.0217236	0.101931	intron-variant	RNF182	GRCh38.p7	6:13960694	GTGTGTGTGTGTGTG[C/T]GCGCGTGCACATGCA	221687
rs570398596	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13967650	TCTGATCATAATCCC[A/G]TACTATTAGAAATTA	221687
rs570399885	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960180	AAGGATCCATTTGCC[C/T]TTACAATCAGCCTCT	221687
rs570484312	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961856	CAACCATTAGGGGTT[A/G]TGGGTATTGTGGGTT	221687
rs570496229	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978176	GGTGTGTTATACTAT[A/G]GGGAGAGCATGGATC	221687
rs570569082	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936113	CTGAGAATTCTGTCG[C/T]GAGATAGCACTATGG	221687
rs570607044	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955196	GGATGTGCATGAATG[C/G]GTACAACTACGTGCC	221687
rs570630135	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963908	AAGTTGCCACACATG[A/T]TAGGGGCTAGGGCAA	221687
rs570672607	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13955992	ATATTTAACATTTCC[A/G]TGGGCTAAAACTTTT	221687
rs570720038	snp	A/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13949829	AAAACTTAAAAAAAA[A/T]TTTGCTGAAGAGTAG	221687
rs570745517	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937032	ATGTTGAGCAGGAGA[A/G]TAAATGATCAGATTT	221687
rs570788699	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13926565	ACCTGTGGAAGATTC[A/G]CAGATGCTCTGCTAA	221687
rs570791948	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956908	CAGTAACAAGCACCA[C/T]CCCCCGCCCCCCACC	221687
rs570794119	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964583	TCCTGGAGCCAGCAG[A/G]CCCCTGAGTGCAAGT	221687
rs570832621	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968708	AACCAAATAAAAAAG[A/G]ATGCACACACACAAA	221687
rs570880179	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13958302	GAAGCAGGAGAATCG[C/T]CTGAACCCGGGAGAG	221687
rs570945185	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922630	ATAAGAAAGACTAGT[C/T]ATGTATCCACACATT	221687
rs570952927	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13958039	CTTCCTAGATGCTAT[-/G]ACTTATAAGTCTTTT	221687
rs570981216	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13948628	TTATCAAGTCAGGAA[A/G]GACTTATTAAGTCTT	221687
rs571004834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952353	TAATCCTGTCACCCA[C/T]AGCTGTCAGCAAAGA	221687
rs571162545	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13965585	AGCTTCTAGACAGAG[A/C]AAATTACTTACCATG	221687
rs571193124	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966200	CTACATAAGAATTTA[A/G]AAATATCATCACCTA	221687
rs571228168	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13973854	CCACCTAAGCTTGCA[A/C]CCCTAAATGCTACAG	221687
rs571278650	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13941146	CTGCTTGTTCTGTCA[A/G]TTACTGGGAAGGATA	221687
rs571314496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944984	AGAAGAACATTTAGC[C/T]GGGCTTAATAAACAT	221687
rs571505088	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13939142	ATATCAGGTAGTATA[A/C]GTTCTTCAGTTTTGT	221687
rs571522477	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13953109	GGGTTTGTTAAGTCC[C/T]GGGTCTGTTCAATAA	221687
rs571556158	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13929695	GAGTGAGGAAACTAA[C/T]ATGATCACTTTCTGT	221687
rs571599883	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949496	TATAAGAAAAAATTA[C/T]GGAAAAAGACACTTG	221687
rs571605098	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952258	TTGTGAAGAGATCTT[C/T]TCCAGCAGGCCGTCA	221687
rs571618272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13930510	TGCTAAGGACTAAGT[A/G]ATACTCCCTTCTCAC	221687
rs571674531	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943308	TTTCTTTTTGTAGAA[A/G]TAGGGTCTCACCGTG	221687
rs571690255	snp	C/T			downstream-variant-500B	RNF182	GRCh38.p7	6:13980059	AGTTATGACTTTGCA[C/T]CTCTGTTAGCTTTAG	221687
rs571701644	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13944022	AAATATAGCTTTGCA[A/G]TTTGGGACAAGATGC	221687
rs571745809	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13932636	CAAAATTAATATTGT[A/G]TAGACATAGTCAAAT	221687
rs571772067	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RNF182	GRCh38.p7	6:13925253	GAGGGGCTGTGCGGC[A/G]GAGGGCGGCTGCGGA	221687
rs571809142	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924599	GTAGTGGTGGAGGGT[A/G]TCTGTGGGGGGGATG	221687
rs571810804	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13933560	TTATTTTTAGTAGTA[G/T]ATTTTATTTAACCTA	221687
rs571891108	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972866	GGGGTTGGAGCCCCC[A/C]CACTGAGTCCCCACT	221687
rs571987144	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939822	TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC	221687
rs571994857	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13932864	TTCCTCATCTCTATA[C/T]TTAATTCTAAACCTT	221687
rs572002392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954616	TTAGTGTATTTTATG[C/T]GTTGCTCAAGACAAT	221687
rs572035236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953887	TTATGCTGTACTAAA[C/T]ATTCAGTAGGCATTT	221687
rs572055485	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13975063	GTACTGTTGTAAGAG[C/G]CTTGTGCTCAGCAGG	221687
rs572136612	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938250	TCTCAATCTCCTGAC[C/T]TCGTAATCTGCCAAC	221687
rs572170182	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961465	GACTCTAGATGCTAT[G/T]TGCTTCCATTGTAGA	221687
rs572208912	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13968038	GACAAAGTGTACTCT[C/T]AGTATGAATTGGGAA	221687
rs572218628	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975636	AATATGTATTAATAA[C/G]TCAACTATTCATGAT	221687
rs572279208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961904	GCTGATGGTCCTTCA[A/G]GAATGAGTACTTGGC	221687
rs572292264	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13975578	GTTACACATTCTTGT[A/G]GAATAGGAAGTCAAT	221687
rs572354117	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966005	TTGAGTGGACTGGAA[A/G]TACTCTCCTGAGGAC	221687
rs572372002	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966565	TACAGGAGTTTGAGA[A/C]CAGCCTGGGCAACAT	221687
rs572408056	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974255	GGGATGCTACCAGAG[C/T]TCAAGGCTGTCACCT	221687
rs572483508	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13926792	TGTGTGTGTGTGTGT[-/G]TTTTTTTTTTTTTCC	221687
rs572499143	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945244	TCTCAGAGTCTGTAC[A/G]TTAGAGAGAGCTGGG	221687
rs572506979	snp	C/T	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13970287	TAACCAACCTCTCTT[C/T]TTTCTCCCTCTCCCA	221687
rs572520921	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13922978	TGGTCCCTCCCTGTT[C/T]TGTATTCAGTTTTTG	221687
rs572523708	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13942705	GGTCTGATCACTTTC[C/T]TCTGCTCCTAGAAGT	221687
rs572565544	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13952549	TGGGATGAAATGTAT[C/G]CTACGGTTTATCCAA	221687
rs572565724	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960268	GACACTTAATAGATA[G/T]TAAGTAAATGCTTGC	221687
rs572603163	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13959521	AAGATTAGAAGCATG[A/C]AGATAAATTAGAAGG	221687
rs572625130	in-del	-/TA			intron-variant	RNF182	GRCh38.p7	6:13945721	TGTTTATTCCCTTGT[-/TA]TATATTCCATTACTG	221687
rs572625780	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953011	TTTCCTTTTGAGATG[A/G]AATGTTACTGCAAAA	221687
rs572676829	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13939483	ACCTTGTAATTTTTT[A/G]TTTCTTGTGTATATA	221687
rs572716245	snp	A/C	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13963396	GCTTATCTATTGTTA[A/C]AAAAGCACCTCAAAA	221687
rs572861592	snp	A/C/G			intron-variant	RNF182	GRCh38.p7	6:13946847	CCTAACAATTTTTAG[A/C/G]GTCTCTTGTATTTAG	221687
rs572876587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956378	CATCCAGGCTGGAGT[A/G]CAATGGTGTGATCTA	221687
rs572884014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956965	ATCCCTTTGTTCTAC[A/G]TCTTCACTAGTAAAT	221687
rs572964120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13949347	TGGCCCCCTTGCTTC[C/T]AAGTGTCCTGAAGCT	221687
rs572992636	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930061	TAGTCAGCCTTGCAT[A/G]TCTGCAGGTTCCACA	221687
rs573017681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948711	GGTGTAAAACACTTT[A/G]TGTTATAAAATAGAA	221687
rs573025170	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13950070	GAAACTTCTCACATT[C/T]CCATGTCTTTTTATA	221687
rs573029463	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943055	GGTAGATTAGTAGAT[A/G]CAAACAGCCCTGATA	221687
rs573034733	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13936457	TAAATTTACATGGTC[A/G]TGGTTGATTGGTCTA	221687
rs573116078	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13970603	CTTTGGATAGATACC[A/T]AGTAGAAGAATTGCT	221687
rs573239386	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969737	GTCCAGGAGCTCAAG[A/C]TAATTTATGAGAATA	221687
rs573249542	snp	C/T	1.64751e-05	0.00287007	missense	RNF182	GRCh38.p7	6:13977694	GGTTGCTAGGTTTGC[C/T]CTACTTCAGCTCCTT	221687
rs573255684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944562	GCAGGGCAAGGAAAG[A/G]TAATTTATGCATGGA	221687
rs573264560	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934353	TAGGCCGTGCCCACC[A/T]GTGTTTGAGATATCT	221687
rs573299585	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13940691	AATGCTACTTAGATT[A/T]TTGATTTTCAACTTT	221687
rs573419224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945031	AAGAGTGTTACTAGA[A/G]ATTTGCTTTCTTAGG	221687
rs573488044	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974322	TTGATGAAGGCTTTC[C/G]TGCTGATGGAATAGG	221687
rs573540295	snp	A/G	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13927776	ATAACATGATTACTG[A/G]TTGGTAATTTAGCAT	221687
rs573647032	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13966595	TGGCAAAACCCCGTC[G/T]CTACTAAAAATACAA	221687
rs573812886	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924711	CTCGCTCCGCTTTAG[C/G]CTTCCCCTCTCGCTG	221687
rs573876507	snp	A/C/G	0.00319098	0.0398384	intron-variant	RNF182	GRCh38.p7	6:13941069	TGCAGAATTTGGTGC[A/C/G]CATAGATTGGGTCAA	221687
rs573878195	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945922	AAACAAGTACATTAA[A/G]GAAGTAAGGGAATAA	221687
rs573936301	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13946271	TCCTGGGTTGAAGCA[A/G]TTCTCCTGCCTCAGC	221687
rs573987682	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923198	TAGCAATTAGGTAGG[A/C]ATTCTTATAGACCTT	221687
rs573992434	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13928892	GGTTGGGAGGGCAGG[G/T]TCAGGGAGTCTGGGG	221687
rs574017565	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13937203	ATATAGAAAAGTGCA[C/T]GAATCGTAAGGATAT	221687
rs574021852	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13951395	TCCCCAAAAAGAGAG[A/G]ATTAGCCCATCCCCT	221687
rs574051024	in-del	-/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13959747	AAAATGGGGAAAACT[-/G]CAGGAAACAATTTGG	221687
rs574058766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13971358	CCTTTGCTCCTTTTT[C/T]GCCTTCTGTCATGAT	221687
rs574090276	snp	A/C	0.000197668	0.00993955	missense	RNF182	GRCh38.p7	6:13977267	GCCAAATGCCTCTAC[A/C]AGATCATAGACTTTG	221687
rs574122805	snp	A/C/G			intron-variant	RNF182	GRCh38.p7	6:13953596	GGCTTATAAAGTGGC[A/C/G]TAAGTCAGGGCCACT	221687
rs574153067	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964922	GCTAGATCACAGGAG[A/G]AGAGACCATTGTGTT	221687
rs574223826	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13972177	GGGCATGGTGGAACG[C/G]GCCTGTAGTCTCAGC	221687
rs574304439	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13958350	GAGATTGCACCACTG[C/T]ACTCCAGCCTGGCAA	221687
rs574366680	in-del	-/A	0.00438332	0.0466095	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923872	TGATTCACAAATGCC[-/A]AAAAATAAATGTCAT	221687
rs574383248	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13925968	TGTGACTGTGAAGAC[-/T]TTTTTTTTTTGGTAC	221687
rs574417616	snp	A/C	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13925395	TACCTTTGGACTTTC[A/C]TGTTTCATGGCATTC	221687
rs574453542	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13925934	ATAGTTTGTTGCAGA[C/G]GCGAAGCACAGATTT	221687
rs574470740	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968244	GTGAGAAAAGAAACA[A/G]TCAGGGGCAGAGGTG	221687
rs574504830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967050	GCCTTGTTTCCTAGG[C/T]TGGTCTCCAACTCTT	221687
rs574547142	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954710	TTCTTTTTTTCCTTG[C/T]AATTTATTTATTGAA	221687
rs574598309	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928508	TTACCAGTTAATTTT[A/G]TAATGTTTTTTTAAA	221687
rs574634308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13968991	TTGTAAGTAACAGAA[A/G]TCCATCCAGAAAACT	221687
rs574677784	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13955432	CAGAATAAATTCTTG[C/T]GTCTTTCCCTTGGTT	221687
rs574749386	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13960393	ATATCTGTAATCCCA[C/G]CACGTTGGGAGGCCA	221687
rs574903083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13964117	CATTATCTAACTAGT[A/G]TATAGAAATACAGGT	221687
rs574977174	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13946227	GCTAGAGTGCAGTGG[C/G]ACAATCTCAGCTCAC	221687
rs575001414	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962414	AAGAAAAATGATGCT[A/G]CAAGTGCTAGAATCT	221687
rs575105512	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957002	TCCACTGTGTGACCG[A/C]ATGGAATGAAATGCC	221687
rs575126383	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13963225	AGAAACTGTATTTTG[A/T]CTGACAGAACTTGCA	221687
rs575175520	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13951274	AGACCTTCAAGGAAC[A/C]GGGTCAGGAAAGCAT	221687
rs575195598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13941196	ATGATGAATTTTTCT[A/G]CCTTTCATTCTGTCA	221687
rs575227342	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13939914	TTAATCTTAATAACT[G/T]ATTTGTAGAATGATT	221687
rs575230773	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13947181	TTATGTTAATCATGC[C/T]TCATGTTTCTTTTGA	221687
rs575257386	snp	A/G	0.00279162	0.0372561	intron-variant	RNF182	GRCh38.p7	6:13971521	TACTGCTATAAGGAT[A/G]CCTGAAAACGTGGGA	221687
rs575280268	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13950142	GCTCCAATAGTCTCA[A/G]TTACATATGTTACAA	221687
rs575296374	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13950997	AGACGGGGTGTCACC[A/G]TGTTGGCCAGGCTGG	221687
rs575355596	snp	A/G	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13941918	AGTTAGTATTTATCT[A/G]TATTTATCATTTATT	221687
rs575403403	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979582	CATTTATGATTTCAT[A/G]AAATCTAGTTTAGAT	221687
rs575406171	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942932	ATACGCCATAAAATT[C/T]ACCCATTGTAGGTGT	221687
rs575418499	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13970467	CAAATAGTAGTTCAC[A/G]TTTTTTTATCCATTC	221687
rs575467551	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13936738	GGAGAGGCATCCAAG[C/T]AAGATTTGGGATTTG	221687
rs575469523	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13943692	TTCAACAAATGTTTG[C/T]TAAGTGAATAATGTT	221687
rs575565515	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923054	TTTTTGTTTTTGCTT[C/T]TTCATTGATAAATTA	221687
rs575580668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13963449	ATTTTATTGGTTCAT[A/G]AGTCTGTGGCTCAGC	221687
rs575594057	snp	G/T	0.00676609	0.0577691	intron-variant	RNF182	GRCh38.p7	6:13938030	TTTTTTTTTTTTTGA[G/T]ACAGAGTTTCTGTCG	221687
rs575648429	snp	A/T	0.000148262	0.00860865	missense	RNF182	GRCh38.p7	6:13977316	TCATTGTCTGTCCTT[A/T]CTGCAGGTTTGAGAC	221687
rs575676575	snp	C/T	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13927278	TGAAAGAAAAAATAC[C/T]ATGATATCTGCAATA	221687
rs575764180	snp	C/T	3.29468e-05	0.00405861	synonymous-codon	RNF182	GRCh38.p7	6:13977746	GGTGTCTAAGAAAGT[C/T]ACCCTTGGGGTCGTC	221687
rs575815214	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967153	GCTGTTTATAAGAAA[C/T]ATTCGAGATAAAGTA	221687
rs575909593	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959611	ATTGGAAGATTGGAA[A/G]CATACTTTGGTTGAA	221687
rs575973855	snp	A/C	0.00398564	0.0444627	intron-variant	RNF182	GRCh38.p7	6:13960495	AAAAACAAACAAACA[A/C]AAACAAAAAACCAAA	221687
rs575974964	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13961051	GACTTATGAGCTTTA[C/T]ATATTATTTGTTGGC	221687
rs576011044	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13928923	CAGGAAGCTGGGGGA[C/T]AGTGATGGCTCTAAT	221687
rs576202755	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13975029	TGGGTGGGCTGAAGT[A/C]TGTGTGTGGCTACCA	221687
rs576232592	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF182	GRCh38.p7	6:13924372	ACCACATCCAGCAGA[C/G]GCAAAGCTTGCTAAA	221687
rs576264889	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925142	CCCAAGCGCGCCGAG[G/T]AGAGGGGGCGGCAAA	221687
rs576303941	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13967957	CCACAAGCTATGGGA[C/T]AGAGTGAAAGCTGTA	221687
rs576379075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13972352	TGAGAAAATTTGCAG[C/T]TTGACGATGCAATAG	221687
rs576427840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13930765	CTTGGTGCCAGGTAC[A/G]CTATTAAGTATTCCA	221687
rs576514961	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF182	GRCh38.p7	6:13959556	GCAATGAACAAGGTC[-/A]AAACCTGGATTAGGA	221687
rs576529704	snp	C/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13952046	TTCAACATGTGGTCT[C/G]TGGGCAAGATGGAAA	221687
rs576559098	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13955501	AAGGAGTTCATTTTG[-/T]TTTTTTAAGTATCAC	221687
rs576569670	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13960729	ATGTACAGTATTAGT[C/T]ACATTTAGTGAAATA	221687
rs576684246	snp	C/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13959428	TTTAAGTGTAATAAA[C/T]GGATGGTAGATATAA	221687
rs576702124	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13944659	TGGCTGAGAAAGAAC[A/G]AATGTTTAGTTAACC	221687
rs576717221	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13958709	TAAGTTAAATTGGGC[C/T]TCTTGAAGTTTGTTG	221687
rs576719068	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13966396	TACATTAAAGGTGAA[C/T]GAACTTGGAAAATTC	221687
rs576744845	snp	C/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969717	AAACAATCATTTGCC[C/G]AATAGTCCAGGAGCT	221687
rs576766510	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924383	CAGAGGCAAAGCTTG[C/T]TAAAAGAGAGAGGAG	221687
rs576768235	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942261	GGGTTCTGTTAAGAT[A/G]TGCTGAGACACTTTT	221687
rs576939646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13948914	ATCTTTTAATATTAC[A/G]TGAAAATCTTGTTCA	221687
rs576953178	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13929326	ATCATCTTCCCTCTT[C/G]TATAGCTATAGTCAT	221687
rs576957577	snp	G/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13954378	GGTTGGTTAGAATTA[G/T]AATCCAAACAAGGAC	221687
rs577083632	snp	A/C	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13956226	AATCTTGGCTATTGG[A/C]TATTGTAATAGTGAC	221687
rs577119045	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13963322	ATAAATGAGGGAAAT[A/G]ATTTCTTTGGGCAGA	221687
rs577138695	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13953821	ATGGGCTCCCCCTCT[A/G]GACTGTATATTTCTT	221687
rs577224648	snp	A/G	0.00119737	0.0244387	intron-variant	RNF182	GRCh38.p7	6:13929999	AGATGTTTTCCAAAG[A/G]TAGTTGTTCCTTAAT	221687
rs577329260	snp	C/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13940577	TTGACTTTTTTTTGC[C/T]ATTGTATGCTTATTT	221687
rs577388948	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933281	CTCACACCTGGAGGC[C/T]GAAGCAGGAAGATCA	221687
rs577510690	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13976378	TTACACTGAGAAGGT[A/T]AGAACAGTCTGCTCT	221687
rs577595456	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934718	TTGTTCATTATTCTC[C/T]TGTCCTGGACAAACA	221687
rs577620118	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13976282	TGTATATGCACAGCT[A/G]TGGTTTTCAAGACTG	221687
rs577635917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13934279	TGTCTCTTATTGTTA[C/T]GGAGTCTCCTGTTGT	221687
rs577642423	snp	C/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13937514	TTGTTTTTTGTCTCT[C/T]TCATTTTGGTATAGT	221687
rs577679539	snp	A/G	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13943793	GACCTCAGTGTTACC[A/G]GAGCTTAACTGAACT	221687
rs577690959	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13938412	TCCACACTGTAGCTT[C/G]CTTTTAACTCTTATA	221687
rs577739138	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13927978	TGCTGTGCACAGTGG[A/G]TATTTGTCAGAACTA	221687
rs577758035	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945847	CAAACCAGACCTCAA[A/G]AGAGGGTTCTTGGAT	221687
rs577794819	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950464	ATGTGAACTAAATGA[C/T]ATTAAAGTTTTTATT	221687
rs577906833	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13974550	TCAAATAATAGCTCA[A/G]TATTTTCAAGGAAAT	221687
rs577908304	snp	A/T	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13957589	AGATGTTGTAGCCAT[A/T]TTTATTAATGCTGGA	221687
rs577930279	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13942790	TTTTTCCTATTTTCC[A/G]TTGTATTTTTTCCTC	221687
rs577976355	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13945613	ATTTTTGTCACTACA[A/G]TGTTTTAACAATTTC	221687
rs577989038	snp	G/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13931644	GATCACTGTGACCTT[G/T]TTTTCTCTTTTTTTT	221687
rs578016790	snp	A/T	0.000798403	0.0199641	intron-variant	RNF182	GRCh38.p7	6:13930912	GGATAAACCACAATC[A/T]GAATTTGACTATGAT	221687
rs578058409	snp	A/G	1.75622e-05	0.00296324	utr-variant-3-prime	RNF182	GRCh38.p7	6:13977910	TTGCCCTGTTTGAGT[A/G]TGAAGTTAGATAATT	221687
rs578099650	snp	C/T	0.00199481	0.0315187	intron-variant	RNF182	GRCh38.p7	6:13972116	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	221687
rs578116193	in-del	-/ATCGGC	0.00517822	0.0506191	intron-variant	RNF182	GRCh38.p7	6:13937761	TGTCCAGGTGGTTAT[-/ATCGGC]GACATTCTCAACATC	221687
rs578193587	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF182	GRCh38.p7	6:13941911	TTTATACAGTTAGTA[-/T]TTATCTATATTTATC	221687
rs745327888	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952655	CTCATCACAGAATAT[A/G]TTACTGGAAAGGGGT	221687
rs745372778	snp	A/G	1.64751e-05	0.00287007	missense	RNF182	GRCh38.p7	6:13977217	ATCTGAAACAGAGGA[A/G]ACCCAAAGTGCTGGA	221687
rs745452121	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13969285	GTCCTGTCTTGTCCC[C/T]AGCTTCAAATAAAGA	221687
rs745468274	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13967309	GGAAAGACATTATAT[-/A]ATGACAAAAAGAGGC	221687
rs745519935	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13926607	TGACGGTAATAAAAT[A/C]GTACATTGATTAAAA	221687
rs745570363	snp	A/C	0.000121178	0.00778293	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977116	ATTGCACACATAATT[A/C]AAGATGGCCAGTCAA	221687
rs745594187	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13927807	CTAGTGCAATGTGTT[A/G]TAGCATTTATAAAAG	221687
rs745666723	in-del	-/AAT			intron-variant	RNF182	GRCh38.p7	6:13928473	TCTCCTTTGTTTTCA[-/AAT]GCCTTCCTTTTTTCA	221687
rs745687828	in-del	-/GTGT			intron-variant	RNF182	GRCh38.p7	6:13960660	GGAGAGAGAGAGTGT[-/GTGT]GTGTGTGTGTGTGTG	221687
rs745748234	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13959505	TAATTTATAGTGGGG[A/C]AAGATTAGAAGCATG	221687
rs745803445	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13948740	AATCTCAGGTCACTG[C/T]AAGTCATTTATTTAG	221687
rs745842065	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978207	CCTCCTTTCGTATTC[A/G]TGGATGTTCTATGAT	221687
rs745895396	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13935424	ACACACAAGATATGT[G/T]TGTGTATCATGACCA	221687
rs745954442	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952767	AAGTTCATGAAGAAA[A/G]TAAGGGAATAAAAAG	221687
rs745994765	snp	C/G	1.64866e-05	0.00287106	missense	RNF182	GRCh38.p7	6:13977454	AGCTGCTGCTCACCC[C/G]CAAGAGGCTGGCCTC	221687
rs746005442	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954069	AAAATGATATAATGA[A/G]TCCCTTTTTACTTAT	221687
rs746013341	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13965615	GAAGAAGTATCACAC[A/T]AGCAGCAGATTTCTC	221687
rs746103315	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13955198	ATGTGCATGAATGGG[C/T]ACAACTACGTGCCCA	221687
rs746203708	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942993	AGTTCTGCAACCAGA[A/G]AAAGAAAATCTTACC	221687
rs746210810	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967998	ACACTATAGTCTTTA[A/G]CTATTTTCAGTATTT	221687
rs746217389	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971961	AAAGCATTCAGTTTT[A/G]TGTATTCACAAAGAT	221687
rs746277788	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979306	TTAAAAAAACATTCT[A/G]GTCTCTAAAACCCAT	221687
rs746293718	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930191	TTACATGGTATTTAC[A/G]TTGTATTAGGTATTA	221687
rs746305229	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13973214	GGGTGTATTTATCCA[A/G]TGCCTGTACCCCCAT	221687
rs746356158	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13931393	GCAACATGCTTTTTG[C/T]TACAGTGGGAGATTT	221687
rs746374512	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13961370	ATTCCATTGAATCCT[C/T]ACAACCACTTTGTGA	221687
rs746457582	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13926905	CCAGATGAAACCCAC[A/T]CTGTGAGTTCTAGCC	221687
rs746491907	in-del	-/A			downstream-variant-500B	RNF182	GRCh38.p7	6:13980259	TATTTATTTTAAAGC[-/A]GGGGAGAAAAATTAG	221687
rs746496323	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971030	TGTAAGTACCACCCC[A/G]GTCAAGAAGAGAGCA	221687
rs746547935	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956211	GGCCACTTGATTCCA[A/G]ATCTTGGCTATTGGC	221687
rs746588256	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971640	CCTAGAGTCTTGGAG[A/G]GCTCAGAGACAGAAA	221687
rs746620691	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13967709	TAGAAATTTAAGAAA[A/C]GTATATAACCTTTTT	221687
rs746676107	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960217	AGGAACCTTGTCTTG[A/G]TTGTCTTTGCATCCC	221687
rs746678988	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965749	AGCCAATCACGAGAC[A/G]ATGAGTATTGCCAAG	221687
rs746845542	in-del	-/GACTGTGCAG			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922536	TGTGGCTAGCAGTTA[-/GACTGTGCAG]CTGAATTAGACTGTG	221687
rs746865928	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13950254	AAGACAAGGACAGAG[A/C]TGTAAAGTCTGACCT	221687
rs746873457	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979712	TTTAAAAAAATGTTC[A/G]TTTTGTTTGAAATGT	221687
rs746989002	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965840	TCTCTGACAGACTAA[A/G]ACCGAGGGCTTATAT	221687
rs747062269	snp	A/G	1.64765e-05	0.00287019	synonymous-codon	RNF182	GRCh38.p7	6:13977362	TGAAGTTAGTAGCCT[A/G]CCCGATGACAACAAC	221687
rs747079036	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13955419	TATAAAGAAAAGGCA[G/T]AATAAATTCTTGTGT	221687
rs747159004	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971251	ATACTGTTCTCATGA[C/T]AGTAAGTTCTCATGA	221687
rs747239928	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13944160	GTTTCTGGGTGGTAG[A/G]GGATTTACATCTCAA	221687
rs747361337	snp	A/G	1.64738e-05	0.00286995	missense	RNF182	GRCh38.p7	6:13977753	AAGAAAGTCACCCTT[A/G]GGGTCGTCTTTGTCA	221687
rs747445628	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962300	AGGTTAGGAACATCG[A/G]GTTTTGTGAATGAGC	221687
rs747482415	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952053	TGTGGTCTCTGGGCA[A/G]GATGGAAAAGCAGAC	221687
rs747527779	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13963300	TAGGTAGGCATGATA[C/T]TCATTGATAAATGAG	221687
rs747663239	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13973092	CTCTTGCATCAGCAT[G/T]ACCTGGATGTGAGAC	221687
rs747697450	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13932433	ACAGATTGGATTTCT[G/T]AAATTATCAGTCTCA	221687
rs747718255	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949406	ACACAAAAAGGCAAG[A/G]GAAAGACTGTGAAAG	221687
rs747718365	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13961310	TCTAAATTTCTAGTC[G/T]CATCCATATAGTGCT	221687
rs747751115	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13962702	ACAACATTTATTTTC[C/T]AGGATGGGAGGAATA	221687
rs747806123	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950329	GCCTTACCTGGAATT[C/T]GCTGTAAAGCAGACA	221687
rs747831862	snp	C/T			downstream-variant-500B	RNF182	GRCh38.p7	6:13980016	CCAAATTTAGAAGTT[C/T]GATTTCTCTGACTTA	221687
rs747845572	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936599	CACTAATGACTCAAA[A/G]ATGAACAAATCAGGT	221687
rs747925908	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965941	GTGAGGGGCCCCTCA[A/G]GGATCTGGTGTGGTG	221687
rs747976187	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937636	GCTATAAACATTCTT[A/G]TACATGTGTATGTGA	221687
rs748006682	snp	A/G	1.6476e-05	0.00287014	missense	RNF182	GRCh38.p7	6:13977343	AGACGTGCCTGCCAG[A/G]TGATGAAGTTAGTAG	221687
rs748026174	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13967132	CTGTGTACCACATCT[C/G]TGGCAGCTGTTTATA	221687
rs748060913	in-del	-/CT			frameshift-variant	RNF182	GRCh38.p7	6:13977467	CCCCAAGAGGCTGGC[-/CT]CTCTGGTCAGTCCTT	221687
rs748102687	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13925414	TTCATGGCATTCTCT[C/T]TGAGGAGGGGTTGGG	221687
rs748112402	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13968651	TTTCTCTAAGATTTC[A/G]TTTGGGGTGGTATTC	221687
rs748214869	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13944342	GTAGGCATGTTAAGG[A/C]GGTGGTTTTGTCATC	221687
rs748222187	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13945755	TGCCTTAATTTCATC[G/T]TGACAGTTTTCCTCT	221687
rs748250782	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13974895	GTCCTTTCTATGGCA[A/C]TGGGGACAGACACTG	221687
rs748336573	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13962429	ACAAGTGCTAGAATC[C/T]CTCATATGTTTTTGA	221687
rs748423450	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13975930	TTACTGCTCCCTTCC[A/G]TTAGTACTGAAAATT	221687
rs748428802	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13959266	CTAAAACATGAAAGA[C/G]TTTGTACTGTTCATG	221687
rs748451965	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13925606	TGGATGGTAAGGGTA[A/G]CCCGGCTTTCCCCGA	221687
rs748511237	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13963359	CTTTGGATTAATTTG[A/G]AAAGAAATAGCATGC	221687
rs748576343	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13952774	TGAAGAAAGTAAGGG[A/T]ATAAAAAGGTGACTA	221687
rs748708436	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13950570	TAACACAATCTTGGC[G/T]CCCTGCAACCTCCAT	221687
rs748830185	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960330	AAAGAGGGCTACATC[A/G]TGAGTCCATCAAGAA	221687
rs748845222	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936761	GGGATTTGGGAATAA[C/T]TGATGTCTATACTGG	221687
rs748959887	snp	A/G	1.64757e-05	0.00287012	synonymous-codon	RNF182	GRCh38.p7	6:13977332	CTGCAGGTTTGAGAC[A/G]TGCCTGCCAGATGAT	221687
rs749005190	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13968931	AAAACACAATAAATT[C/G]TCAACGTCAAGTACA	221687
rs749035267	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13925586	GGTGCAGTTGCACCT[A/G]TAACTGGATGGTAAG	221687
rs749081933	in-del	-/GA			intron-variant	RNF182	GRCh38.p7	6:13975359	CACATGGAAGGAAAG[-/GA]GAGAGAGAAGAGTTG	221687
rs749121205	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13934275	ACCCTGTCTCTTATT[G/T]TTATGGAGTCTCCTG	221687
rs749133444	in-del	-/AATA			intron-variant	RNF182	GRCh38.p7	6:13968731	CACACAAAGGCCACT[-/AATA]AATAAATAAATATGT	221687
rs749138584	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13931930	TGCCCTTATAAAAGA[A/G]ACCCCAGAGAGGTCA	221687
rs749155497	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957378	AATAAAATTTAATCT[A/G]TAGTTCTTTTTCTTC	221687
rs749331069	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13947560	TCTTAGATTAGACTT[C/T]TTAAAGCCTTGAGAC	221687
rs749339762	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933169	AAACCCTTCTTTTCA[A/G]GTAGTATTGATTTTT	221687
rs749365759	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933999	CTCCAGCCTGGGCAA[C/T]AGGGGAAGACTCGGT	221687
rs749382804	snp	A/T	1.64765e-05	0.00287019	missense	RNF182	GRCh38.p7	6:13977621	ACTGTGTCACACAAC[A/T]GGACTGTGTGGAACT	221687
rs749383189	in-del	-/TTG			intron-variant, cds-indel	RNF182	GRCh38.p7	6:13925311	GGAGCTGCCCCTCTG[-/TTG]TTGTTGTTATTTTCC	221687
rs749431338	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13956641	GTCCTTTGCGTTAGA[C/G]TACTCTATAATGTTC	221687
rs749530009	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13964434	ACAAATTTCCATTTT[C/T]CCATCTAGGTAAATA	221687
rs749575612	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13953561	TTCACGAGTCATGGA[A/T]TAGGCAGTGTGAAGC	221687
rs749580920	snp	A/C	4.94368e-05	0.00497152	missense	RNF182	GRCh38.p7	6:13977547	GAGAGAGCTCCCCGT[A/C]CCTGAGCTCCACTCC	221687
rs749666076	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13955168	CATTGTAGTAGGAAT[A/G]CAGCGTTGGACGGGA	221687
rs749782889	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13971770	ATGGAGATGAGGAAC[A/T]TGTTGAGAACTGGAA	221687
rs749854648	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13968224	AACAATTTAGAAGAC[C/T]ATAAGTGAGAAAAGA	221687
rs749900858	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	RNF182	GRCh38.p7	6:13977323	CTGTCCTTTCTGCAG[A/G]TTTGAGACGTGCCTG	221687
rs749995093	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13974502	ACTCAGTAATCTGAT[-/A]AGAGTATTTCTGTGA	221687
rs749998980	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13953603	AAAGTGGCGTAAGTC[A/G]GGGCCACTTAGAGAA	221687
rs750000657	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13965003	TGAACCCCAGTGATA[C/T]AACAAAGAAAAATAT	221687
rs750092784	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954687	ATCCTTGGTCTGTGG[A/G]TTCACCCTTCTTTTT	221687
rs750244103	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962056	CTTAATTCTGAGACC[A/G]TCGTCTCTACAAAGT	221687
rs750304187	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930836	CCTCATCTATAAAAG[A/G]CTAATAAATAGCTTA	221687
rs750418828	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13950135	ATACCTTGCTCCAAT[A/T]GTCTCAATTACATAT	221687
rs750438924	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13946839	TATTCCTGCCTAACA[A/G]TTTTTAGGGTCTCTT	221687
rs750552447	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951170	CAACACATATAAATA[C/T]ACGGAGAGATGGAAG	221687
rs750573378	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936323	GACAATGATGGAAGA[A/G]TTAGAAATCCTTAAA	221687
rs750648009	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922643	GTCATGTATCCACAC[A/G]TTAATTTTTAAGCTT	221687
rs750677078	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936494	TAAATTTTTCTTTCA[C/T]AGGCAGTTTAAAAAG	221687
rs750745542	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13967989	CCAGTGGAAACACTA[A/T]AGTCTTTAGCTATTT	221687
rs750779906	in-del	-/TGAG	5.19755e-05	0.00509755	utr-variant-3-prime	RNF182	GRCh38.p7	6:13977905	ACACATTGCCCTGTT[-/TGAG]TGTGAAGTTAGATAA	221687
rs750806817	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926699	AACAGCAAATAGGAT[A/G]TTGAAGCCTAGGCAC	221687
rs750835133	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956998	CCTGTCCACTGTGTG[A/G]CCGAATGGAATGAAA	221687
rs750837040	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13925993	TGGTACTTAGACATC[A/G]TCTTACATGTAGTAA	221687
rs750900681	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13958581	GCAGGTATTTATTAT[C/G]TACTCTGTGCTAGCT	221687
rs750989922	in-del	-/TTGGCTA			intron-variant	RNF182	GRCh38.p7	6:13956215	ACTTGATTCCAAATC[-/TTGGCTA]TTGGCTATTGTAATA	221687
rs751068114	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13955015	TGACCTGTGTGTCAT[C/T]CGCCTCCTTATCTGT	221687
rs751145541	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926512	ATTAACAGTTTGCAG[A/G]TTATTTCACAATTGG	221687
rs751152141	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13942584	TGTCCTCAACTGATC[G/T]ACTTGCCTCAGCCTA	221687
rs751224223	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13972796	GGCAGAAGTTTGCTG[C/T]AGGGGTGGGGCCCTC	221687
rs751316380	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13973998	GAAGGCAGGTTGGAG[A/T]TGGGCTGGAATGAGT	221687
rs751355241	snp	A/C	1.64846e-05	0.0028709	missense	RNF182	GRCh38.p7	6:13977514	ACTGCCTGGTCATAA[A/C]CATCATGGAGGTGCA	221687
rs751471659	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13942668	ATTCTCAGCAGCTAT[C/T]TCATCAAATAGTATT	221687
rs751531771	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937188	TGAAGGTTAACATAC[A/G]TATAGAAAAGTGCAC	221687
rs751615610	snp	G/T	1.77808e-05	0.00298162	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977076	TAATCAAAGCCATTC[G/T]TCAACAAGACCCACC	221687
rs751716979	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13924671	AGGAGTGCCTACTAG[C/G]ATGCGAATACCACTT	221687
rs751722064	snp	A/C/T	6.59375e-05	0.00574153	missense	RNF182	GRCh38.p7	6:13977445	ACCCTACTGAGCTGC[A/C/T]GCTCACCCCCAAGAG	221687
rs751876653	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13945511	AGTGTTTAGTGTGAT[C/G]CTATAGGTTAGGCAA	221687
rs751956546	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13947161	TAGAATAGTGATTCA[A/G]ATTTTTATGTTAATC	221687
rs752099090	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13956915	AAGCACCACCCCCCG[C/G]CCCCCACCATACACA	221687
rs752211367	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13974186	CAAGAGGAACAATCA[C/T]CATGCTCTTTTCTGC	221687
rs752212684	snp	C/T	3.29527e-05	0.00405898	missense	RNF182	GRCh38.p7	6:13977586	AATTTTATAGGCCTG[C/T]GAGTTTCGACTCTGT	221687
rs752280446	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922533	CATATGTGGCTAGCA[A/G]TTACTGAATTAGACT	221687
rs752297440	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13962128	GGACTGAGGCCAACA[A/T]ATTATTGTTAGTAAT	221687
rs752386529	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932035	ACCTAATCTGCCAGC[A/G]CCTTAATCTTGGACT	221687
rs752410878	snp	A/G	3.29712e-05	0.00406011	synonymous-codon	RNF182	GRCh38.p7	6:13977491	CAGTCCTTCTCACAC[A/G]TCCTCCAACTGCCTG	221687
rs752441611	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13951543	ATTAGCTGTCCCTAA[A/G]AGTATATGTCCTACC	221687
rs752488054	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13963051	AGGAAAGATACTTCA[A/G]TGGATGTTCATATGC	221687
rs752617168	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938848	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	221687
rs752651026	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926460	TAATGCCACTTCATT[A/G]GAAGATTGTATTGGA	221687
rs752720526	snp	A/G	3.3279e-05	0.00407902	synonymous-codon	RNF182	GRCh38.p7	6:13977839	TTGTCATGAATTTCT[A/G]GACTGTATGGCACCT	221687
rs752745116	in-del	-/CTC			intron-variant	RNF182	GRCh38.p7	6:13948847	TAATGTCTCTTTTCT[-/CTC]CTTTCTTTTTTTTTC	221687
rs752789215	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13970335	GTTTTTTAGCTCCCA[C/T]ATGAGTGAGAACATG	221687
rs752792710	in-del	-/AAAC			intron-variant	RNF182	GRCh38.p7	6:13960482	CCCCGTCTTTACAAA[-/AAAC]AAACAAACACAAACA	221687
rs752843368	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13927347	CCATGGTTTAGCCAC[C/T]TGGTGGAAGCAGGCA	221687
rs752874157	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13958593	TATCTACTCTGTGCT[A/T]GCTTATGATAGGTGC	221687
rs752877359	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971350	AAGATGTGCCTTTGC[C/T]CCTTTTTCGCCTTCT	221687
rs752924546	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13961685	CCTCTCTTCCAAAAT[C/T]AATAACTTAGATTGC	221687
rs752945209	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13948204	TTCGTTTTAATGGCA[C/T]ACATTTCAAAGCTGT	221687
rs752957817	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13947341	TTTTCTCTCTCCAGT[C/G]CCTATTTTTATTTAA	221687
rs752965159	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959601	ATGGAATGAAATTGG[A/G]AGATTGGAAACATAC	221687
rs753008849	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13949062	ATTTTCACAAACCTT[G/T]TATAACCCTTTAAAT	221687
rs753063957	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964369	CTTTATGTAATAGCC[A/G]CTGAACATGCTTAGT	221687
rs753148542	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13973771	TATGTCTTTATTAGC[-/A]GCATGAGAATGGACT	221687
rs753164375	snp	C/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978881	TGAGATGCTTCAGCT[C/T]ACAGTTTGAAGTGCT	221687
rs753215136	snp	A/G	1.64768e-05	0.00287021	missense	RNF182	GRCh38.p7	6:13977199	TCTGTTACAATCGAT[A/G]CAATCTGAAACAGAG	221687
rs753215201	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933716	CAATTTGGAGGATAT[A/G]TTTTCAGCAGTTAAA	221687
rs753237573	snp	C/G	3.29804e-05	0.00406068	missense	RNF182	GRCh38.p7	6:13977480	GCCTCTCTGGTCAGT[C/G]CTTCTCACACGTCCT	221687
rs753271723	in-del	-/C			intron-variant	RNF182	GRCh38.p7	6:13931349	CAATAAATGTCATAT[-/C]CCCCAGGCTAAATTC	221687
rs753289826	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13947022	CAACAGCAATATATT[C/T]TACAACTGTAAAGCG	221687
rs753323626	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933711	CATCTCAATTTGGAG[A/G]ATATATTTTCAGCAG	221687
rs753334325	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13932130	TTTGTTAGAGCAATC[C/T]GAGCAGACTAAGACA	221687
rs753345826	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13963216	AGAATACATAGAAAC[G/T]GTATTTTGACTGACA	221687
rs753365211	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13975482	TGTATTTGAAAAAAT[C/G]CTACCTACATTTTTG	221687
rs753401748	snp	C/T	1.64817e-05	0.00287064	missense	RNF182	GRCh38.p7	6:13977424	GGAAGAAGTGCCTGC[C/T]AGAGAACCCTACTGA	221687
rs753412338	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13951541	CCATTAGCTGTCCCT[A/G]AAAGTATATGTCCTA	221687
rs753453135	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RNF182	GRCh38.p7	6:13977308	ACAAGGTGTCATTGT[C/T]TGTCCTTTCTGCAGG	221687
rs753532571	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13963991	GGGTAATATCATGAA[A/G]AAGTGGGGAAGAAGA	221687
rs753675855	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940810	AATATTTAAAAATAT[C/T]CATGTGTTTTTTCTT	221687
rs753718696	in-del	-/AGTA			intron-variant	RNF182	GRCh38.p7	6:13946951	GATACCTGGAAGATT[-/AGTA]AGTATTTAAGAAAAC	221687
rs753725695	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971463	GTATATCTTTATTAG[C/T]GTAAGAATCAACTAA	221687
rs753726409	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13970620	GTAGAAGAATTGCTG[A/G]GTTGTAAGGTATTTC	221687
rs753764100	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942363	AAAATTTTTTTTGAG[A/G]CAAAATCTTGCTCTG	221687
rs753852029	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13929019	CATTTCCAGAGGCTG[G/T]CTAGTCCTACAAAAG	221687
rs753892118	snp	C/G	1.65362e-05	0.00287538	missense	RNF182	GRCh38.p7	6:13977818	GTATGGTTTTTGCCA[C/G]TGTGTTTGTCATGAA	221687
rs753945617	snp	A/C	1.64738e-05	0.00286995	missense	RNF182	GRCh38.p7	6:13977711	TACTTCAGCTCCTTA[A/C]CCTTAGGAATCTACT	221687
rs753965350	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13958909	TAATGCTCTTCTTTG[C/G]GGGTGAATGAATTCT	221687
rs754020023	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13948584	AATATGCCATTATTG[A/G]ACTTCAGGGGACCTA	221687
rs754088198	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13935394	ACTGTCAATTCAGCA[G/T]TTTCCATATTTCACA	221687
rs754107734	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949769	GTAAATTGTACCAAC[A/G]AATAGGTAAACATAC	221687
rs754173907	in-del	-/GTA			intron-variant	RNF182	GRCh38.p7	6:13970112	GTCAGGGTAATTAGG[-/GTA]GTATTCATCACCTTA	221687
rs754224630	in-del	-/TTGC			intron-variant	RNF182	GRCh38.p7	6:13966676	GCTGAGGCGGGAAGA[-/TTGC]TTGACCCCGCGGGGT	221687
rs754261087	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13975740	TGTCTAGCGCAGTTA[A/C]TCTCTGCCCTCAGAA	221687
rs754312689	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13931368	CAGGCTAAATTCCCT[C/T]AGGGTCAGAGCAACA	221687
rs754347957	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924165	CTCAGGGCTCATGGT[A/G]GATGCTTAGCGGTCA	221687
rs754366327	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956113	CATATTGCTGCAGAT[A/G]ACAAGATTTCATTCT	221687
rs754546688	snp	A/G	1.64814e-05	0.00287061	missense	RNF182	GRCh38.p7	6:13977430	AGTGCCTGCCAGAGA[A/G]CCCTACTGAGCTGCT	221687
rs754598423	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13929973	ATAGAAACTAGAATA[A/C]TTTATGAAAAAGATG	221687
rs754600546	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943738	ACACTTTTAAAAATG[A/G]TAAGACATATTTTAT	221687
rs754612915	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13972918	GTGAGAAGAGGGCCA[C/T]TGTCCTCCAGACCCC	221687
rs754628260	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13974110	TGAGGGATCTTAAAA[C/T]CATAATAAGATAGAT	221687
rs754657580	snp	C/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978123	CCAGAGAAAGGACAG[C/G]GTTTCTCTCAGCACT	221687
rs754690493	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930977	TTCTGCTGCAGTGAA[A/G]ATGCTTTTGGGATTA	221687
rs754720403	snp	C/G/T			intron-variant	RNF182	GRCh38.p7	6:13950301	GGACCAGGCTAATTC[C/G/T]ATACATCTCAAGGCC	221687
rs754758859	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961979	TTATTATAGTGAGAA[A/G]GATTTTTTTGAATGG	221687
rs754788884	snp	C/G	4.94262e-05	0.00497098	missense	RNF182	GRCh38.p7	6:13977334	GCAGGTTTGAGACGT[C/G]CCTGCCAGATGATGA	221687
rs754842799	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13966631	AGCTAAGCGTGGTGG[C/T]GCACACCTGTAATCT	221687
rs754963565	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13937445	GTGTGTGTGTATGAT[A/C]GCTTTCACCAACTAT	221687
rs754980891	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13938755	AAAATAAGTAATCAT[A/G]TGCTTGTGAATCTCT	221687
rs755005748	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13968464	GAATCATATGAAATT[A/G]CAGCTGAGTTTTATG	221687
rs755148967	snp	A/T	3.29468e-05	0.00405861	stop-gained	RNF182	GRCh38.p7	6:13977738	TACTTACTGGTGTCT[A/T]AGAAAGTCACCCTTG	221687
rs755154185	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13940720	TTTCTAACATATGCA[G/T]TCGAAGCTCTGCATT	221687
rs755251766	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956794	CTCAACCACAAATAT[A/G]GGAAGAATGTATTTA	221687
rs755264051	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13958357	CACCACTGCACTCCA[A/G]CCTGGCAACAGAGCA	221687
rs755309842	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932613	TCCTTTGAATATTTT[A/G]TCACTTACAAAATTA	221687
rs755371798	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13944599	GGATGAAACCAGAAA[C/T]GGGGTGGAAATTAGG	221687
rs755389841	snp	G/T			missense	RNF182	GRCh38.p7	6:13977525	ATAACCATCATGGAG[G/T]TGCAGAGAGAGAGCT	221687
rs755399750	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933815	CTGAGGTCGGTAGTT[C/T]GAGACCAACCTGGCC	221687
rs755473224	snp	A/G	1.7561e-05	0.00296314	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977100	ACCCACCTGGCATAA[A/G]ATTGCACACATAATT	221687
rs755490328	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13963303	GTAGGCATGATACTC[A/C]TTGATAAATGAGGGA	221687
rs755564177	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13947355	TCCCTATTTTTATTT[A/C]AACAAACCATGGTAG	221687
rs755579567	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13964330	AACAGTTAACTTAGG[G/T]ATGAGTATCAGTTTG	221687
rs755664476	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13931173	AAAGAGACAGAGAAC[C/G]CCTATCCTCAAGTCT	221687
rs755682631	snp	C/T	1.64814e-05	0.00287061	synonymous-codon	RNF182	GRCh38.p7	6:13977419	CAAAGGGAAGAAGTG[C/T]CTGCCAGAGAACCCT	221687
rs755741332	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940931	TATTGTCAAAGAACA[C/T]GCTATTAACATTTTA	221687
rs755795777	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13951590	AGGCTAAAAGCTCTC[A/G]TAATGCAAGTGATTT	221687
rs755879765	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937703	TCATGGGTTATATGT[A/G]TGATTTAGCTGTGAT	221687
rs755881842	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952534	ACTTTGTCCTTTACC[C/T]GGGATGAAATGTATC	221687
rs756021199	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13931413	GTGGGAGATTTCCTT[-/G]TTTTAGGATGCCGAA	221687
rs756071330	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13968798	TGTTTATGTGTACAT[A/G]TGCATGCATGTGTGC	221687
rs756076302	in-del	-/TATC			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923322	TTAATAAGAAATCAA[-/TATC]TATGAATTTTATATA	221687
rs756118344	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13927451	CTGCATTTTAGCTTA[C/T]GGGTTTTAATTTTAT	221687
rs756136763	snp	C/T	1.64762e-05	0.00287016	missense	RNF182	GRCh38.p7	6:13977615	GTCACCACTGTGTCA[C/T]ACAACTGGACTGTGT	221687
rs756162679	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13957302	TGTTGCAAAGTGACA[C/T]ATTCATTAAGATTGA	221687
rs756378691	snp	A/G			missense	RNF182	GRCh38.p7	6:13977820	ATGGTTTTTGCCAGT[A/G]TGTTTGTCATGAATT	221687
rs756379879	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13948285	AACTGCCTTTTGAAG[A/G]GAATCAAAACAAGAC	221687
rs756467731	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935240	TCTAATTTTACATTT[A/G]TTTATGTGATCGATT	221687
rs756601005	in-del	-/TG			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979267	GTTGGCAAAATAGAC[-/TG]TTCACAGAAACTAGG	221687
rs756612755	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13962123	ATTGGGACTGAGGCC[-/A]AACATATTATTGTTA	221687
rs756644250	snp	C/T			intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925305	GCTCAGGGAGCTGCC[C/T]CTCTGTTGTTGTTGT	221687
rs756762956	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13933746	AGTGAGGCCAGGCAT[C/G]GTGGCTTATGCCTGT	221687
rs756783215	snp	C/T	6.59022e-05	0.00573993	synonymous-codon	RNF182	GRCh38.p7	6:13977200	CTGTTACAATCGATA[C/T]AATCTGAAACAGAGG	221687
rs756822746	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13963217	GAATACATAGAAACT[A/G]TATTTTGACTGACAG	221687
rs756967338	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13939079	CAAGAGCAAGACCCT[A/G]TCTCAAAAAAACAAA	221687
rs756982470	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940829	GTGTTTTTTCTTTGA[C/T]CATAAGTTATTAGAC	221687
rs757000817	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13970635	GGTTGTAAGGTATTT[A/C]TATTTTTAGTTTTTT	221687
rs757024299	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13926590	TGCTAAATACTCTTT[C/G]ATGACGGTAATAAAA	221687
rs757107139	snp	A/G	1.64836e-05	0.0028708	missense	RNF182	GRCh38.p7	6:13977521	GGTCATAACCATCAT[A/G]GAGGTGCAGAGAGAG	221687
rs757168846	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13942823	TAGTTTGGAAACTTT[C/G]TAATGACCTATGTTT	221687
rs757204372	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13958779	AAGGGATTTTGAAAA[C/T]GAGTAATTGGAGAGG	221687
rs757305380	snp	A/G	1.77647e-05	0.00298027	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977080	CAAAGCCATTCTTCA[A/G]CAAGACCCACCTGGC	221687
rs757357501	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13935403	TCAGCATTTTCCATA[G/T]TTCACACACACAAGA	221687
rs757400142	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13948600	ACTTCAGGGGACCTA[A/T]TATCTAAAAGGATTA	221687
rs757544436	snp	G/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924117	CTGAGTGCCATGGCC[G/T]GCAGTACGTGACCAG	221687
rs757661981	snp	A/T	1.71708e-05	0.00293003	utr-variant-3-prime	RNF182	GRCh38.p7	6:13977894	AGAAATTGGACACAC[A/T]TTGCCCTGTTTGAGT	221687
rs757752976	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13973119	AGACATGGAGTCAAA[G/T]ATTTGGCTGCCCTGC	221687
rs757788418	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952569	GGTTTATCCAAAGTC[A/G]GCCAATTGGTGCTGT	221687
rs757872377	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967085	TCAAGTGATCCACCT[A/G]TCTTGGCCTCCCAAA	221687
rs757964898	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13953795	CAAGCGTGGTAATGG[A/C]TGAGTTCCTTATGGG	221687
rs758060994	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13954692	TGGTCTGTGGGTTCA[C/G]CCTTCTTTTTTTCCT	221687
rs758091057	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971596	AAGGCTCAGAAGAAG[A/G]CAGGAAAATGTGGGC	221687
rs758094101	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13929697	GTGAGGAAACTAATA[G/T]GATCACTTTCTGTTA	221687
rs758120632	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13960074	GGAAGACTGTGATGT[A/C]ATGGAACCTGTGAGA	221687
rs758172836	snp	C/T	1.6486e-05	0.00287102	missense	RNF182	GRCh38.p7	6:13977496	CTTCTCACACGTCCT[C/T]CAACTGCCTGGTCAT	221687
rs758184870	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13972686	TTGGCAGCTTCCATG[C/T]GGCATTGAGCCTGTG	221687
rs758208694	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13948923	TATTACATGAAAATC[A/T]TGTTCAAAAGAGAAA	221687
rs758227865	snp	G/T	1.64841e-05	0.00287085	synonymous-codon	RNF182	GRCh38.p7	6:13977443	GAACCCTACTGAGCT[G/T]CTGCTCACCCCCAAG	221687
rs758389297	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950143	CTCCAATAGTCTCAA[C/T]TACATATGTTACAAT	221687
rs758420108	in-del	-/TTTATTTTA			downstream-variant-500B	RNF182	GRCh38.p7	6:13980237	TTTATTTTATTTTAT[-/TTTATTTTA]TTTATTTATTTATTT	221687
rs758495642	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933847	ATGTGGTGAAACCCC[A/G]TCTCCACTAAAAATA	221687
rs758535352	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13936378	CATAATTAGGAGAAG[C/G]TTAAAGCATTTTAGA	221687
rs758560577	snp	C/T	1.64738e-05	0.00286995	missense	RNF182	GRCh38.p7	6:13977750	TCTAAGAAAGTCACC[C/T]TTGGGGTCGTCTTTG	221687
rs758602688	snp	C/T	8.43832e-05	0.00649496	synonymous-codon	RNF182	GRCh38.p7	6:13977860	TATGGCACCTCCTTC[C/T]TAACTGATATGCAAA	221687
rs758622236	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13937180	TTTGTTATTGAAGGT[A/T]AACATACATATAGAA	221687
rs758746522	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957066	TATTCAAACTAGAGT[A/G]ACTCCATCTTGCATA	221687
rs758750848	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13944043	GACAAGATGCCCACC[A/G]GTTAGGCTCTTACCC	221687
rs758760637	snp	C/T	1.64754e-05	0.00287009	missense	RNF182	GRCh38.p7	6:13977309	CAAGGTGTCATTGTC[C/T]GTCCTTTCTGCAGGT	221687
rs758931921	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13974579	ATAATTTAGGTTCAC[A/G]TAATTATCAGCTAGA	221687
rs758955735	snp	A/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979653	AGTAAATACCATGTT[A/T]AGAAGATGTTTTGTG	221687
rs758972195	in-del	-/C			utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974257	GATGCTACCAGAGCT[-/C]AAGGCTGTCACCTGG	221687
rs759008233	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924051	TACTTTTCTCTCCCT[C/T]TCTAAGAATTTCCTC	221687
rs759020018	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13975503	TACATTTTTGGCTAC[C/T]AGAGATTCTATAGAT	221687
rs759035730	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956680	CTTAATGTATCTTGG[C/T]TCACTACAAAAGTGT	221687
rs759133578	snp	G/T	1.64882e-05	0.00287121	synonymous-codon	RNF182	GRCh38.p7	6:13977482	CTCTCTGGTCAGTCC[G/T]TCTCACACGTCCTCC	221687
rs759274571	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945028	CATAAGAGTGTTACT[A/G]GAGATTTGCTTTCTT	221687
rs759292048	in-del	-/GAT			intron-variant	RNF182	GRCh38.p7	6:13965749	AGCCAATCACGAGAC[-/GAT]GAGTATTGCCAAGGA	221687
rs759362529	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13931882	TGGGAGGTGATTAGG[A/C]CATGAGGGTGGAGCC	221687
rs759362893	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13975171	GGACTGTGTGTGGTG[A/G]CCAGGATAGAACTCC	221687
rs759462748	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933328	CAAGACCAGCTTGGG[C/T]AACATAGTGAGATCC	221687
rs759492599	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13963625	TGGGCCTTTCTCTCT[A/G]TGGTTTCTCATCTTC	221687
rs759582661	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13953247	CAAGAAGGAGTCACT[C/G]TAGTTTGAACACTTC	221687
rs759638601	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13961573	ATAGGGTGCGGAGTA[C/G]CTGGTTTTTTTCTCT	221687
rs759718393	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940049	CTAGGACCTCAATTA[C/T]AATTTTGAATAGAAA	221687
rs759767854	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928408	ACTTGTTTCTCAGCT[A/G]TTAGGATTATTTATT	221687
rs759770673	in-del	-/GGA			cds-indel	RNF182	GRCh38.p7	6:13978597	TTATCTGAGAAGAAT[-/GGA]GGAGAAGGAACTTCT	221687
rs759776544	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13970270	TGTATGTTTGTACCC[A/G]TTAACCAACCTCTCT	221687
rs759800264	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13959446	ATGGTAGATATAATC[C/T]CATTTACATTTTTAG	221687
rs759905203	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933261	AGAATTGGCCAGGTG[C/T]GTGTCTCACACCTGG	221687
rs759964894	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13972798	CAGAAGTTTGCTGCA[-/G]GGGTGGGGCCCTCAT	221687
rs759989098	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964001	ATGAAAAAGTGGGGA[A/G]GAAGACCCAAAAACA	221687
rs760104297	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13949449	GGTTTCTTTGACTTC[A/C]TTCTGGCCTTTGGTT	221687
rs760210780	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13945228	AGTGATTTACTCAAG[A/C]TCTCAGAGTCTGTAC	221687
rs760361221	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13932999	TTTGAAATTGCTGTC[C/T]GAGCATTTTTTAATT	221687
rs760413069	snp	C/T			utr-variant-5-prime	RNF182	GRCh38.p7	6:13977020	CCTGCCTTTTTGCAT[C/T]GCTGCCAGATTTGGA	221687
rs760436355	snp	C/T	3.29968e-05	0.00406169	missense	RNF182	GRCh38.p7	6:13977799	GCCTCGTTATTCTTA[C/T]GGTGTATGGTTTTTG	221687
rs760503203	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13963887	ATTGCAGCCATATTT[C/G]CAGACAAGTTGCCAC	221687
rs760626973	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954177	AAACAAAGCCCAGAT[A/G]TCATATTATTTCATC	221687
rs760768121	snp	A/G	1.64732e-05	0.0028699	missense	RNF182	GRCh38.p7	6:13977286	TCATAGACTTTGGGG[A/G]CTCCCCACAAGGTGT	221687
rs760821173	snp	C/G/T	3.29556e-05	0.00405918	stop-gained, synonymous-codon	RNF182	GRCh38.p7	6:13977191	GTGCAAAATCTGTTA[C/G/T]AATCGATACAATCTG	221687
rs760828288	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971359	CTTTGCTCCTTTTTC[A/G]CCTTCTGTCATGATT	221687
rs760867772	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928866	TGCAGGGGTGGGGGT[A/G]CGGTGGTGGTGGTTG	221687
rs760895029	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13930405	ATATACATGTAAATC[C/T]ATCTTGGAAATGTTG	221687
rs760916148	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13959608	GAAATTGGAAGATTG[G/T]AAACATACTTTGGTT	221687
rs760916216	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13972128	ACACGGTGAAACCCC[A/G]TCTACTAAAAAATAC	221687
rs761002173	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936009	CATGGCACAAGGCCA[A/G]GGGAAAAGAGGCACA	221687
rs761002512	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13960788	AATTGTAGAAATGGT[A/T]CATATAACCTATGCT	221687
rs761023450	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13931012	ACTTTGGAAAGAGTG[G/T]CAGTTGAGGACTGCC	221687
rs761096797	snp	C/G			utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13961499	CCTGCAAGGGATGGT[C/G]ATACTCCTGGCTGCA	221687
rs761183489	snp	C/G	1.64768e-05	0.00287021	missense	RNF182	GRCh38.p7	6:13977665	GTTTCAGACATCCAT[C/G]CGGGTGTTAGTGTGG	221687
rs761259116	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936970	GAAAGGAGTAAGAGA[C/T]GTGGCTGGTGAGGTA	221687
rs761285455	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13947974	AGGTAGAGAGAAAGA[A/C]ATGTGCTCTAAATTT	221687
rs761399697	snp	C/T	6.59011e-05	0.00573988	missense	RNF182	GRCh38.p7	6:13977339	TTTGAGACGTGCCTG[C/T]CAGATGATGAAGTTA	221687
rs761499214	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964163	TAGAACTTGAAAGGC[A/G]TTATTTAGGAAAGAT	221687
rs761713664	snp	C/G	1.64735e-05	0.00286993	missense	RNF182	GRCh38.p7	6:13977261	GTTTGTGCCAAATGC[C/G]TCTACAAGATCATAG	221687
rs761785138	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961023	AAAGAGTAAGGTACT[A/G]AGCAAAAACCTAGAC	221687
rs761845177	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13930646	CTATGTGAAAAGTAG[G/T]ACTAAATAAGAGACA	221687
rs761845879	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978260	GTTGCTCTGAGACAC[A/G]AAGTGTGTACTCCTT	221687
rs761853224	in-del	-/TG/TGT			intron-variant	RNF182	GRCh38.p7	6:13969133	TGTTGTTGTTGTTGT[-/TG/TGT]TTTACCTCTGCCTCT	221687
rs761881177	in-del	-/G	1.64737e-05	0.00286994	frameshift-variant	RNF182	GRCh38.p7	6:13977753	AAGAAAGTCACCCTT[-/G]GGGTCGTCTTTGTCA	221687
rs761921336	snp	C/T	1.65562e-05	0.00287712	missense	RNF182	GRCh38.p7	6:13977154	AAGACACTGCGGAGT[C/T]TCAGGCCTCTGATGA	221687
rs761935763	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13973480	ACCTTATATTGTAAT[A/C]ATCCCCACATGTCAA	221687
rs761975242	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13966512	TCATACCTGTAATCC[C/G]AGCACTTTGGGAGGC	221687
rs762067378	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936241	GGTGGGGACACAGAG[C/T]CAAACCATATCAGTA	221687
rs762241165	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937075	GTCTCTCATGGTGTT[A/G]CATATAGACTTTTCA	221687
rs762290428	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	RNF182	GRCh38.p7	6:13977560	GTCCCTGAGCTCCAC[C/T]CCTGTGGTAGAATTT	221687
rs762329504	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938426	TGCTTTTAACTCTTA[C/T]AATTTTTCAATGAGA	221687
rs762353538	snp	A/G/T	3.29773e-05	0.00406051	missense	RNF182	GRCh38.p7	6:13977474	AGGCTGGCCTCTCTG[A/G/T]TCAGTCCTTCTCACA	221687
rs762408013	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13935769	TGTTTAAAAATAAGA[C/T]ATCTTACTATGATTC	221687
rs762413632	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13956974	TTCTACATCTTCACT[A/G]GTAAATCACCTGTCC	221687
rs762477344	snp	G/T	6.58989e-05	0.00573978	synonymous-codon	RNF182	GRCh38.p7	6:13977677	CATCCGGGTGTTAGT[G/T]TGGTTGCTAGGTTTG	221687
rs762522271	snp	A/G	3.29511e-05	0.00405887	missense	RNF182	GRCh38.p7	6:13977589	TTTATAGGCCTGCGA[A/G]TTTCGACTCTGTCAC	221687
rs762551998	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13926466	CACTTCATTAGAAGA[C/T]TGTATTGGAAACTAA	221687
rs762616765	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13926587	CTCTGCTAAATACTC[-/T]TTCATGACGGTAATA	221687
rs762641383	in-del	-/TACTGA			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922535	TATGTGGCTAGCAGT[-/TACTGA]ATTAGACTGTGCAGC	221687
rs762721236	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13955930	TAGGTATGAAAATAT[A/G]TGGTTTTCAAATTCA	221687
rs762775374	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943708	TAAGTGAATAATGTT[A/G]AAGTTTTGCAGCCGA	221687
rs762817699	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13973915	TTAATGGACTCATAC[A/T]GTATTACTCTTTTGG	221687
rs762859773	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930874	TTGTACAGAGTTGGT[A/G]GATTTAAAAACATGA	221687
rs762915470	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951201	AAGATCTAATAGTTA[C/T]AATATTTTTTATTTG	221687
rs762986786	in-del	-/GATCTGGTGTGGT			intron-variant	RNF182	GRCh38.p7	6:13965942	GAGGGGCCCCTCAAG[-/GATCTGGTGTGGT]GATCTGGTGTGGTGA	221687
rs762992623	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13929089	CCTCCCAATTAACTA[A/C]AACGTGACTCTCTTG	221687
rs763067940	in-del	-/TGTC	1.64751e-05	0.00287007	frameshift-variant	RNF182	GRCh38.p7	6:13977305	CCCACAAGGTGTCAT[-/TGTC]TGTCCTTTCTGCAGG	221687
rs763070048	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13962744	AGAGTTGAAATTTGA[C/G]AGTTGTCTTTTCATA	221687
rs763110882	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13941846	TTTTGGAATCGTTGT[A/T]TCAGTTTAATTCCAC	221687
rs763366670	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926015	ATGTAGTAATATGAA[A/G]GAAAACAGATACATT	221687
rs763380918	snp	C/T	1.64895e-05	0.00287132	missense	RNF182	GRCh38.p7	6:13977466	CCCCCAAGAGGCTGG[C/T]CTCTCTGGTCAGTCC	221687
rs763456924	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13927144	CTGCTTGGTTGTAGT[A/G]GCTTATTAATAAGAG	221687
rs763517440	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13932122	TATGGTATTTTGTTA[C/G]AGCAATCTGAGCAGA	221687
rs763637046	in-del	-/C			intron-variant	RNF182	GRCh38.p7	6:13926725	GGCACATTATATAGA[-/C]AGAGAATGTAGTTTT	221687
rs763717759	snp	A/G	1.64754e-05	0.00287009	stop-gained	RNF182	GRCh38.p7	6:13977679	TCCGGGTGTTAGTGT[A/G]GTTGCTAGGTTTGCT	221687
rs763718739	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13963900	TTGCAGACAAGTTGC[C/T]ACACATGATAGGGGC	221687
rs763757858	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933611	TTTCAACATGTAATC[A/G]ATATAAAAATTATTA	221687
rs763771023	snp	A/C/T	3.29529e-05	0.00405901	missense, synonymous-codon	RNF182	GRCh38.p7	6:13977593	TAGGCCTGCGAGTTT[A/C/T]GACTCTGTCACCACT	221687
rs763772390	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13963149	AGCTTTTTAAAAAGA[C/T]TTGAATTAATAGAAG	221687
rs763812745	snp	A/G	8.23893e-05	0.00641778	missense	RNF182	GRCh38.p7	6:13977193	GCAAAATCTGTTACA[A/G]TCGATACAATCTGAA	221687
rs763929720	snp	A/G			utr-variant-5-prime, intron-variant	RNF182	GRCh38.p7	6:13974359	AGAGCTGGCCTTGGA[A/G]TTAGAGTAGGTATAT	221687
rs764040007	in-del	-/GAT	1.64757e-05	0.00287012	cds-indel	RNF182	GRCh38.p7	6:13977342	GAGACGTGCCTGCCA[-/GAT]GATGAAGTTAGTAGC	221687
rs764051395	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13954208	TGTGAAACCTCAGTA[C/T]GTATCTTCAAAACAT	221687
rs764101324	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13972159	AAAAAAAAAAAATTA[G/T]CTGGGCATGGTGGAA	221687
rs764155481	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13928991	AGATTACCTGAGGTC[G/T]TTACCTAGTGACCAT	221687
rs764181777	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13948447	GTTATACCAGAATTA[A/T]AGTAGTTTTGCATAA	221687
rs764278944	in-del	-/GTGT			intron-variant	RNF182	GRCh38.p7	6:13960657	GGAGGGAGAGAGAGA[-/GTGT]GTGTGTGTGTGTGTG	221687
rs764282933	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13959640	AATTGACTGGCTTGC[C/T]AATGGATTGGACATG	221687
rs764315385	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13934012	AACAGGGGAAGACTC[A/G]GTCTCAAAAACAGGA	221687
rs764380215	snp	G/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979098	TGCTATCCCTGTTGT[G/T]TTTGAGTTGGTTTTG	221687
rs764411437	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964543	TCTCAATTCTACTCT[A/G]TCTGCCTTTCCTGAT	221687
rs764549564	snp	G/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924126	ATGGCCTGCAGTACG[G/T]GACCAGTCCTTGGCA	221687
rs764564656	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13956312	CTGACTGTTCTTTGC[-/T]TTTTTTTTTTTTTCC	221687
rs764673354	snp	G/T	3.29592e-05	0.00405938	synonymous-codon	RNF182	GRCh38.p7	6:13977410	TTGTGGAGGCAAAGG[G/T]AAGAAGTGCCTGCCA	221687
rs764719326	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13934690	GCTGGCAGCTCCATT[C/G]CTTTTTTCTAGTTTG	221687
rs764763741	snp	A/C	1.64882e-05	0.00287121	missense	RNF182	GRCh38.p7	6:13977484	CTCTGGTCAGTCCTT[A/C]TCACACGTCCTCCAA	221687
rs764773327	snp	C/T	8.23839e-05	0.00641757	synonymous-codon	RNF182	GRCh38.p7	6:13977365	AGTTAGTAGCCTGCC[C/T]GATGACAACAACATC	221687
rs764851653	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13954426	AATAAATCTCTTAGG[A/C]TTTTAGTCTATAGCA	221687
rs764858089	snp	G/T	0.000131807	0.00811701	missense	RNF182	GRCh38.p7	6:13977581	GGTAGAATTTTATAG[G/T]CCTGCGAGTTTCGAC	221687
rs764861356	snp	C/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978676	TATAACATCTTAGTT[C/T]TGGTTTTTTTAAACC	221687
rs764914044	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13938004	ATCTTTTTCTTACTG[-/T]TTTTTTTTTTTTTTT	221687
rs764925081	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13948374	AGGAAATTTGGCCCC[-/T]TGTGGCACACAATAA	221687
rs764949202	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13964971	TTCAGTTCCATGGGT[C/T]CTTCAACAATCAGAC	221687
rs764949649	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942378	ACAAAATCTTGCTCT[A/G]TGGCCCAGGCTGGAG	221687
rs765034366	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13939607	GGAGTGCAGTGGCGC[A/G]ATCTGGGCTCGCTGC	221687
rs765056169	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13969962	GACATACTTTAGCAC[C/T]TGTTCTTATCAAGGC	221687
rs765113322	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13929285	TATTTGAGTGAGAAG[C/T]TGTGTTTCTGATCAG	221687
rs765140397	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13960280	ATATTAAGTAAATGC[-/T]TGCTGAATTATTAAA	221687
rs765154520	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13973638	CTCTTGCCTGCCGCC[A/G]TGTAAGACATGCCTT	221687
rs765169295	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943552	GTACTTATCTTACCG[C/T]CTTGGAACTGCTATA	221687
rs765195772	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13972497	AGAGGTCTTTATGGC[A/G]GCCCCTCCCATCACA	221687
rs765196821	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13930761	TTTACTTGGTGCCAG[C/G]TACGCTATTAAGTAT	221687
rs765218690	in-del	-/AG			intron-variant	RNF182	GRCh38.p7	6:13965890	AATGTATAAGAAAAC[-/AG]GAACTAGAGAGGGGC	221687
rs765347767	snp	G/T	1.6615e-05	0.00288223	missense	RNF182	GRCh38.p7	6:13977836	TGTTTGTCATGAATT[G/T]CTAGACTGTATGGCA	221687
rs765355949	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13964068	CAGTTAAGAAAAACA[C/T]GAATTTTTTAAAATG	221687
rs765418717	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13949955	CACACAGAATTTCTT[C/T]TACAAGATTAATTTT	221687
rs765496606	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	RNF182	GRCh38.p7	6:13977374	CCTGCCCGATGACAA[C/T]AACATCCTTGTAAAC	221687
rs765582705	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RNF182	GRCh38.p7	6:13977299	GGACTCCCCACAAGG[C/T]GTCATTGTCTGTCCT	221687
rs765607011	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13925978	GAAGACTTTTTTTTT[C/T]GGTACTTAGACATCA	221687
rs765700373	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13956979	CATCTTCACTAGTAA[A/C]TCACCTGTCCACTGT	221687
rs765724095	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13945263	GAGAGAGCTGGGCTT[G/T]ATTTAGCCAAAAATT	221687
rs765863960	snp	G/T	1.64814e-05	0.00287061	synonymous-codon	RNF182	GRCh38.p7	6:13977422	AGGGAAGAAGTGCCT[G/T]CCAGAGAACCCTACT	221687
rs766078041	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13975320	TCCTGAATGGGATCA[-/G]GATCAGGAATGAGGG	221687
rs766079904	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13930968	AAAATGCCTTTCTGC[G/T]GCAGTGAAGATGCTT	221687
rs766085720	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13942430	CACTGCAACCTCTGC[C/T]TCCTGGGCTTAGGTG	221687
rs766091829	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13956064	TTTCTGTGCCTGGCT[G/T]CTTTCACTTCACATA	221687
rs766180854	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943717	AATGTTAAAGTTTTG[C/T]AGCCGACACTTTTAA	221687
rs766185799	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13973983	GCTTTTGACAGAAGT[G/T]AAGGCAGGTTGGAGA	221687
rs766321309	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13958721	GGCTTCTTGAAGTTT[A/G]TTGAAGGAAGTAAAC	221687
rs766387113	snp	G/T	1.65124e-05	0.00287331	synonymous-codon	RNF182	GRCh38.p7	6:13977809	TCTTATGGTGTATGG[G/T]TTTTGCCAGTGTGTT	221687
rs766450570	snp	G/T	1.64732e-05	0.0028699	missense	RNF182	GRCh38.p7	6:13977705	TTGCTCTACTTCAGC[G/T]CCTTACCCTTAGGAA	221687
rs766568433	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF182	GRCh38.p7	6:13977287	CATAGACTTTGGGGA[C/T]TCCCCACAAGGTGTC	221687
rs766614179	in-del	-/ACTC			intron-variant	RNF182	GRCh38.p7	6:13966231	TTTTCTGACAAAGAT[-/ACTC]AATAATACAAAGAAA	221687
rs766652297	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957067	ATTCAAACTAGAGTG[A/G]CTCCATCTTGCATAG	221687
rs766688035	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13970110	CAAGTCAGGGTAATT[A/G]GGGTATTCATCACCT	221687
rs766691284	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13933119	ATGGACAGGCTTGGC[C/G]CTCCTGTGTAGTCAT	221687
rs767018705	in-del	-/AT			intron-variant	RNF182	GRCh38.p7	6:13926097	GATTTGTTTTAAATC[-/AT]ATTTAAACAATATGA	221687
rs767059928	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956770	TACCAACGGCTGAGC[C/T]CTTTTTCTCTCAACC	221687
rs767123979	in-del	-/C			intron-variant	RNF182	GRCh38.p7	6:13943585	TGCATACATGCCTGT[-/C]CCCCCTCTGTGAATT	221687
rs767176665	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13974121	AAAATCATAATAAGA[G/T]AGATGAAACTTTTTT	221687
rs767211280	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13930627	TTTCAGGAGCTTATT[C/T]AAGCTATGTGAAAAG	221687
rs767228560	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962127	GGGACTGAGGCCAAC[A/G]TATTATTGTTAGTAA	221687
rs767229323	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945134	ATAGAGCCCTGTTAT[A/G]TTGGAGCTGGAAGGT	221687
rs767303207	in-del	-/TA			intron-variant	RNF182	GRCh38.p7	6:13928347	TCCTTCTATATATTC[-/TA]TGTTGCTTGATGAAA	221687
rs767314500	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13962993	TGTTTTTTTGAGCTC[C/T]ACTTATTTTGACTTT	221687
rs767404380	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952479	AACCCCTTACGTCTC[A/G]GGAGGGATGCTAACC	221687
rs767405676	snp	A/G	1.64735e-05	0.00286993	missense	RNF182	GRCh38.p7	6:13977697	TGCTAGGTTTGCTCT[A/G]CTTCAGCTCCTTACC	221687
rs767417393	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13933424	CAAAGGCTGAGGTAG[A/G]ATGAGGCAGGAGGAT	221687
rs767490028	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13940296	TTATTTTGTCAATAT[A/G]GTAATCACATTTTAA	221687
rs767492534	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13953258	CACTCTAGTTTGAAC[A/G]CTTCTGACAGATTCC	221687
rs767523651	in-del	-/G			intron-variant	RNF182	GRCh38.p7	6:13938173	CCTGGCTAATTTTTT[-/G]TATTTTTTTTTTTTT	221687
rs767630181	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926345	GTCAGGCAAAGAGTG[A/G]TTATTTAATATTCCT	221687
rs767731886	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13970308	CCCTCTCCCACCTCA[C/T]CCTGAGATAAAGTTT	221687
rs767732985	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13926682	TTTCTCACTTAAGCA[C/T]GAACAGCAAATAGGA	221687
rs767781798	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13936315	TCTGTACAGACAATG[A/T]TGGAAGAGTTAGAAA	221687
rs767821803	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13971316	CTTGGCATTCATTCT[C/G]TCTTGCCTGTCACCA	221687
rs767822675	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13928492	TTCCTTTTTTCAAAA[A/G]TTACCAGTTAATTTT	221687
rs767841405	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13959532	CATGAAGATAAATTA[C/G]AAGGTTCTGCAATGA	221687
rs767864362	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949497	ATAAGAAAAAATTAC[A/G]GAAAAAGACACTTGC	221687
rs767926144	in-del	-/T	1.64822e-05	0.00287068	frameshift-variant	RNF182	GRCh38.p7	6:13977778	TGTCAGCCTGGTCCC[-/T]TTCGAGCCTCGTTAT	221687
rs767927118	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13948167	GAATACATTAGTTTT[C/G]CAAGAGTCTTGGAAG	221687
rs767962862	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935063	CTTTGTGTAGAGATG[A/G]TCTGGGAAAGATGGG	221687
rs767978947	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965132	AAATAGAAAGAGCAC[A/G]TAAGGAGATGCAGAT	221687
rs768141933	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13942806	TTGTATTTTTTCCTC[-/T]TTAGTTTGGAAACTT	221687
rs768148417	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13947820	CATGTCAGTCATTCC[A/G]GTCAAAGCCTTGGTA	221687
rs768224629	snp	C/T	1.64825e-05	0.00287071	synonymous-codon	RNF182	GRCh38.p7	6:13977779	TGTCAGCCTGGTCCC[C/T]TCGAGCCTCGTTATT	221687
rs768236211	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13934371	GTTTGAGATATCTCC[C/T]TTCATTCTGTTGGAT	221687
rs768255696	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13927952	TAAATATCAGGTATT[C/G]TTAACTGACCTGCTG	221687
rs768391159	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13949233	TGTCCACTGGACGTT[C/T]TAGTCATATTCAGAC	221687
rs768484988	snp	G/T			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978414	GCCAAGAGGAAACTC[G/T]GTTCCATTCCCTTGG	221687
rs768487542	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935567	TGACTTACAAGCTAC[A/G]TATTAATAAGTAGAA	221687
rs768509778	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964825	GTTCCACAAGAGACC[A/G]AGGAGAAAAATCCAT	221687
rs768511046	in-del	-/ACA	3.29522e-05	0.00405894	cds-indel	RNF182	GRCh38.p7	6:13977370	GTAGCCTGCCCGATG[-/ACA]ACAACATCCTTGTAA	221687
rs768587531	snp	C/T	3.32535e-05	0.00407746	missense	RNF182	GRCh38.p7	6:13977148	CTCCTGAAGACACTG[C/T]GGAGTCTCAGGCCTC	221687
rs768720018	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943405	GGATTAGAGGCCTGA[A/G]CCACTGTGCCTGGCT	221687
rs768727155	in-del	-/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924137	ACGTGACCAGTCCTT[-/G]GGCACAGAGTCACTC	221687
rs768773377	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956438	CAATTGATTCTCCTG[C/T]CTCAGCCTCCCTAGT	221687
rs768813614	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13930410	CATGTAAATCTATCT[G/T]GGAAATGTTGATCCA	221687
rs768814711	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13974734	TCATAAACACTCACA[A/T]GTCTACTCTAGCTTT	221687
rs768888174	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13973456	GCTGTGTGTCCCCAC[C/G]CAAATCTGACCTTAT	221687
rs768950310	snp	A/G	1.64754e-05	0.00287009	missense	RNF182	GRCh38.p7	6:13977637	GGACTGTGTGGAACT[A/G]CACGTCCCTGCTGTT	221687
rs769013783	snp	A/G	1.64784e-05	0.00287035	missense	RNF182	GRCh38.p7	6:13977558	CCGTCCCTGAGCTCC[A/G]CTCCTGTGGTAGAAT	221687
rs769143737	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13957831	TAAGGACAAAGTATA[C/G]TTCTTCAGGTTGACA	221687
rs769146360	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13950925	CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGT	221687
rs769146539	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13962366	TTATCAATAGCTGAG[C/T]GTAAAAACCAATGTT	221687
rs769234601	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13952102	AAAAGATAGTAAAGA[C/G]ACAGGAGAGAGAGAG	221687
rs769297718	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938898	GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT	221687
rs769299156	snp	C/T			downstream-variant-500B	RNF182	GRCh38.p7	6:13980049	GTTAAAATTCAGTTA[C/T]GACTTTGCACCTCTG	221687
rs769324171	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952661	ACAGAATATGTTACT[A/G]GAAAGGGGTCCCAGT	221687
rs769376060	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13935715	ATGGATAGAAGTTAC[G/T]CAGCAATGTATCTTA	221687
rs769381847	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950399	GACCTTAACACATTT[A/G]CCAAGGACAGTATTC	221687
rs769466102	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936626	AGGTATAGCCCTACC[C/T]TCCTGAGGCTAACAG	221687
rs769528690	snp	C/T	1.64741e-05	0.00286998	missense	RNF182	GRCh38.p7	6:13977220	TGAAACAGAGGAAAC[C/T]CAAAGTGCTGGAGTG	221687
rs769542720	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13925471	ATTTTTACGAATCTC[A/T]GAAAAGTGAGCCCAT	221687
rs769609377	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923510	GTGTGTTTCTGTATG[A/G]CAGATCTCTAGAATT	221687
rs769632014	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13955895	CTATCTCTATGCCCT[A/C]CCCATTTTCATACCT	221687
rs769655518	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13944464	GTTGCAGTTTGTATA[C/G]GTCAAAGTGGAGGCC	221687
rs769718518	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13967136	GTACCACATCTCTGG[C/T]AGCTGTTTATAAGAA	221687
rs769780130	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959772	ATTTGGTGGTAGTGA[A/G]AGGTGAGGGTTGAAA	221687
rs769781940	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13928475	TCCTTTGTTTTCAGC[-/T]CTTCCTTTTTTCAAA	221687
rs769862637	snp	A/G	1.64882e-05	0.00287121	missense	RNF182	GRCh38.p7	6:13977457	TGCTGCTCACCCCCA[A/G]GAGGCTGGCCTCTCT	221687
rs769868204	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926268	AATGAAAACAGTACC[A/G]CTGATCATTTTGAAT	221687
rs769902547	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13945772	GACAGTTTTCCTCTG[C/T]CTTTTTGGCATCCCA	221687
rs769966439	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13976083	AAGAGTTTGCATGAA[A/G]TAAAGTAGATGAGTA	221687
rs770118945	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13935437	GTGTGTGTATCATGA[A/C]CAAATAAATTATTGT	221687
rs770225110	in-del	-/TTT			intron-variant	RNF182	GRCh38.p7	6:13950806	TGCACTCCCCCTTTA[-/TTT]TTTTTTTTGAGATAG	221687
rs770283261	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952886	TAAGATAACAAAGCA[A/G]AAAGTCGTAGGGAGA	221687
rs770340980	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971070	ACTCCATAGCCTGCA[C/T]TAAGTCTGCTTGGAC	221687
rs770341957	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951953	TCAACCTGGCAAGGC[C/T]CAAACTTGCCCCTTT	221687
rs770363350	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13939908	CACTTCTTAATCTTA[A/T]TAACTTATTTGTAGA	221687
rs770391007	snp	A/G	1.75197e-05	0.00295966	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977104	ACCTGGCATAAGATT[A/G]CACACATAATTCAAG	221687
rs770414581	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936846	GTGGGTAAAAGAGCT[A/G]TAAAGAGGGAACAGG	221687
rs770450227	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13967394	TGTAAAACAAAACTG[C/T]TAGAAATGCAAATAT	221687
rs770502560	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923887	AAAAAATAAATGTCA[C/T]GTTCCCCAGGGTTTG	221687
rs770596672	in-del	-/C			intron-variant	RNF182	GRCh38.p7	6:13964837	ACCAAGGAGAAAAAT[-/C]CATAGTTGGGTGCGT	221687
rs770602889	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13925658	GCAGTACCGATACTT[G/T]GTCAAGGAGATACTT	221687
rs770825724	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13975114	GGTGGCAGATCACCA[A/G]TGAACTGCCCAGGGC	221687
rs770864500	snp	C/T	3.29712e-05	0.00406011	synonymous-codon	RNF182	GRCh38.p7	6:13977449	TACTGAGCTGCTGCT[C/T]ACCCCCAAGAGGCTG	221687
rs770887674	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949643	ATCAGAAGTTATCAT[A/G]ATCGAACAAACCTGA	221687
rs771007372	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13963469	TGTGGCTCAGCATTT[C/T]CTACTGGGCTCAGTG	221687
rs771068878	snp	C/T	1.64773e-05	0.00287026	missense	RNF182	GRCh38.p7	6:13977364	AAGTTAGTAGCCTGC[C/T]CGATGACAACAACAT	221687
rs771093537	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13964597	GACCCCTGAGTGCAA[C/G]TGAAACCCCAAGCTT	221687
rs771216544	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971150	GGCTCTGTTTCCCCA[C/T]CCAAATCTCACCTTG	221687
rs771284680	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13965824	CCTTCTCAAATCCAT[C/G]TCTCTGACAGACTAA	221687
rs771381872	snp	C/T	9.88419e-05	0.00702931	synonymous-codon	RNF182	GRCh38.p7	6:13977758	AGTCACCCTTGGGGT[C/T]GTCTTTGTCAGCCTG	221687
rs771429749	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971874	TTTGAACTTGAGAGA[A/G]ATGATTTAGGGTATG	221687
rs771514413	in-del	-/AAAT			intron-variant	RNF182	GRCh38.p7	6:13963364	GATTAATTTGGAAAG[-/AAAT]AGCATGCTATTTTGC	221687
rs771601578	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13925795	CTGGAGGCAGGTAGC[A/T]GGGCGGTGTTTGCAT	221687
rs771628752	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13965297	AAGTACAGAACAAAA[A/G]TATAAAGGAATGGAA	221687
rs771672285	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13946274	TGGGTTGAAGCAATT[C/G]TCCTGCCTCAGCCTC	221687
rs771706683	in-del	-/C			intron-variant	RNF182	GRCh38.p7	6:13954137	TGCTTCATTTATCTG[-/C]CCCCCTCCCCATTGG	221687
rs771803945	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959073	CCTGAGATCCTCTTC[A/G]TATGCAGATGTCCAG	221687
rs771866786	snp	C/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13978347	CTCTTAAGTCACTCT[C/G]TGTGGTCGGCGATCC	221687
rs771897839	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13947754	TAGGGGCTTTAATTG[G/T]CTCTATAAATGAATT	221687
rs771949835	snp	A/T	1.64751e-05	0.00287007	missense	RNF182	GRCh38.p7	6:13977347	GTGCCTGCCAGATGA[A/T]GAAGTTAGTAGCCTG	221687
rs772170314	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935465	TGTAGCTGGCAGGAA[A/G]GTATTCCTAAAGTCA	221687
rs772196184	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13965710	AAGGGTTTGGTCTAG[G/T]CCCTACTTGCTCACC	221687
rs772311952	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930206	ATTGTATTAGGTATT[A/G]TAAGCAATCTACAGA	221687
rs772321787	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13943077	GCCCTGATAGAGCTA[C/T]AGTTATTTAATTACA	221687
rs772365564	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13928390	TCTTATAGTTGGGGA[A/C]TTACTTGTTTCTCAG	221687
rs772434540	snp	C/T	1.6477e-05	0.00287024	missense	RNF182	GRCh38.p7	6:13977561	TCCCTGAGCTCCACT[C/T]CTGTGGTAGAATTTT	221687
rs772485156	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13972089	GCAGATCACGAGATC[A/G]GGAGATCAAGACCAT	221687
rs772565365	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13931426	TTGTTTTAGGATGCC[A/G]AAGGTCTGGAGTGTG	221687
rs772573129	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13973364	AGACATTGGGGGACT[C/G]TTGGGAGGGCACGAT	221687
rs772578864	snp	A/C			intron-variant, upstream-variant-2KB	RNF182	GRCh38.p7	6:13925040	TAAGGCGATCGCGCC[A/C]GCGGCCGGGGAGGGG	221687
rs772584011	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13961441	CCAGGTCCCAAATCT[C/T]GGTCTCCTGACTCTA	221687
rs772675800	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950607	GGTTCAACAATTCTC[A/G]TGCCTCAACCTCCCG	221687
rs772727699	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13935768	ATGTTTAAAAATAAG[A/C]CATCTTACTATGATT	221687
rs772797565	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923571	TGAATTCTGGCAGGT[A/G]TTGCCAAATGCTTAA	221687
rs772817792	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936687	CACAAGTGTGTGCCA[C/T]GATGGGGCATATGTG	221687
rs772829294	snp	G/T			downstream-variant-500B	RNF182	GRCh38.p7	6:13980064	TGACTTTGCACCTCT[G/T]TTAGCTTTAGATAAC	221687
rs772908208	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943572	GAACTGCTATATTTT[A/G]CATACATGCCTGTCC	221687
rs772996954	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13965951	CCTCAAGGATCTGGT[G/T]TGGTGATCTGGTGAG	221687
rs773000321	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13957991	TGAAGACAAAGAATG[G/T]AATTCTTTTATTTTT	221687
rs773086967	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13955908	CTCCCCATTTTCATA[A/C]CTTTATTAGGTATGA	221687
rs773087040	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967249	ATATAAGCTTTAGAT[A/G]AGGTATAAAGGTTGA	221687
rs773091815	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13953629	GAGAAAGGAAATTTC[A/T]CCTTAGAAGAGCAAA	221687
rs773137461	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973775	TCTTTATTAGCAGCA[C/T]GAGAATGGACTAATA	221687
rs773177360	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932910	AGTTACCCACTAGAA[A/G]GAAGTTTATAATCTC	221687
rs773184509	snp	G/T	4.94271e-05	0.00497102	missense	RNF182	GRCh38.p7	6:13977358	ATGATGAAGTTAGTA[G/T]CCTGCCCGATGACAA	221687
rs773187704	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13942272	AGATATGCTGAGACA[C/T]TTTTTCTTTACTGTC	221687
rs773237421	snp	A/G	1.64732e-05	0.0028699	missense	RNF182	GRCh38.p7	6:13977270	AAATGCCTCTACAAG[A/G]TCATAGACTTTGGGG	221687
rs773262784	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13931746	TACGACCTTGAGGTA[C/G]CTGCTTAATCTCTCT	221687
rs773288415	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952165	GTGGGGCTGGGAGGC[A/G]AGGAGCTCAGGGAGA	221687
rs773393225	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13951810	GACCCATAGGCAAAG[-/T]ACTCTCAGTTTTGCA	221687
rs773472612	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13963386	ATGCTATTTTGCTTA[C/T]CTATTGTTACAAAAG	221687
rs773499536	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13930796	CACAAGCTGTCTCTT[C/T]TGATTGTCACCATAA	221687
rs773499621	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962757	GACAGTTGTCTTTTC[A/G]TAAGGGGAAAAATAT	221687
rs773562574	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952892	AACAAAGCAAAAAGT[C/T]GTAGGGAGATGTGCT	221687
rs773576357	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	RNF182	GRCh38.p7	6:13977659	CCTGCTGTTTCAGAC[A/G]TCCATCCGGGTGTTA	221687
rs773589679	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961027	AGTAAGGTACTAAGC[A/G]AAAACCTAGACTTAT	221687
rs773670149	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13936867	AGGGAACAGGGCATC[A/C]TAAAAGCTTAGAATC	221687
rs773674636	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13932319	ATTTTCTTTAGGCCT[G/T]TAAGTTCAACTTGCA	221687
rs773702040	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13958162	GGAGGCCGAGGCAGG[A/C]AGATCACGAGGTCAA	221687
rs773720923	in-del	-/TGTT			intron-variant, utr-variant-5-prime	RNF182	GRCh38.p7	6:13925309	AGGGAGCTGCCCCTC[-/TGTT]GTTGTTGTTATTTTC	221687
rs773760563	in-del	-/TTAG			intron-variant	RNF182	GRCh38.p7	6:13942962	TAGCATTCAATGATC[-/TTAG]TTAAATTCACAGAGT	221687
rs773821177	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13927128	TCATGTATTGCATGC[A/G]CTGCTTGGTTGTAGT	221687
rs773909260	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13973626	GGCATTCATTGTCTC[C/T]TGCCTGCCGCCATGT	221687
rs773940657	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13929582	CCTTTATGAATTCTT[C/G]CCTATGGGCCAGACA	221687
rs773953004	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967472	GTGATAACCTTGCAC[A/G]TACCTTGATGATTCA	221687
rs773963459	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13925659	CAGTACCGATACTTT[A/G]TCAAGGAGATACTTG	221687
rs774037335	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13931824	CAAATTCATATGTTG[A/G]AATTCTAACTCCCAA	221687
rs774150999	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945898	AGGTGAGTCCACAGA[A/G]TAAAGTGAAAACAAG	221687
rs774181872	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13975129	GTGAACTGCCCAGGG[C/T]TGGGGACTGTCCCAT	221687
rs774203686	snp	A/G	6.63526e-05	0.0057595	synonymous-codon	RNF182	GRCh38.p7	6:13977149	TCCTGAAGACACTGC[A/G]GAGTCTCAGGCCTCT	221687
rs774357727	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13963538	TTCAAACAGGTGTTG[A/T]CCCTGGTGGTTAGTT	221687
rs774412616	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13940045	CTATCTAGGACCTCA[A/G]TTATAATTTTGAATA	221687
rs774423839	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13972661	CTTCAGAGGGTGCAA[C/G]CCCCAAACCTTGGCA	221687
rs774485632	in-del	-/TTG			intron-variant	RNF182	GRCh38.p7	6:13969106	GCTTGTCTCTGTTTT[-/TTG]TTGTTGTTGTTGTTG	221687
rs774503933	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938911	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	221687
rs774534994	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13954068	GAAAATGATATAATG[A/G]ATCCCTTTTTACTTA	221687
rs774603197	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13966500	AGGCATGGTGGCTCA[C/T]ACCTGTAATCCCAGC	221687
rs774711664	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13960522	CAAACCCAACTGTTA[C/T]TCTTTTAAGTGAATT	221687
rs774752259	in-del	-/TTTTTTTATT			downstream-variant-500B	RNF182	GRCh38.p7	6:13980199	AAAAGGCCTTCATAG[-/TTTTTTTATT]TTATTTTATTTTATT	221687
rs774781653	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13927212	GAAAACAATAATCTG[G/T]CATGTTTATATGTGT	221687
rs774823165	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13948152	TTTCTCAATATTTAT[A/G]AATACATTAGTTTTC	221687
rs774867764	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13928280	GCCAATTTTTTGTAG[C/T]AGTTATGGAGTATGG	221687
rs774984202	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13941526	AATAGTTCATTTACA[C/T]GTAAAGTACTTGATA	221687
rs774986324	snp	G/T	1.6489e-05	0.00287128	synonymous-codon	RNF182	GRCh38.p7	6:13977473	GAGGCTGGCCTCTCT[G/T]GTCAGTCCTTCTCAC	221687
rs775053782	in-del	-/AGAC			intron-variant	RNF182	GRCh38.p7	6:13931162	TTTTAGAGTAGAAAG[-/AGAC]AGAGAACCCCTATCC	221687
rs775083632	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13947759	GCTTTAATTGGCTCT[A/G]TAAATGAATTTTGAT	221687
rs775094637	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13946212	TGCTCTGTTGCCCAG[A/G]CTAGAGTGCAGTGGC	221687
rs775101973	snp	C/T			utr-variant-5-prime	RNF182	GRCh38.p7	6:13976988	CTGGAAGATTTCTGG[C/T]TTCTTTCACTACTTA	221687
rs775126605	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13934065	GTGGCCTTACCAAAA[A/T]AGTAATGTTGTATTT	221687
rs775195858	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13946308	AGCAGCTGGAACTAC[A/C]GGCATGTGCATTATG	221687
rs775275624	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13974173	TAGCCTGGCTTTTCA[A/G]GAGGAACAATCACCA	221687
rs775358638	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13933577	TTTTATTTAACCTAA[C/T]ATATCAAAATTACCA	221687
rs775393933	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13953288	CTTGGTGTGGAAACT[C/G]TGTGGCATTTCATTC	221687
rs775450950	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13934328	GGGCCAAGCCTGTCT[A/G]TGTCAGCTTTAGGCC	221687
rs775578046	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942101	TGTCAGTTTCTTTCA[A/G]TACTTTAAAGATGTA	221687
rs775668062	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943251	TATACAATGTAAGGT[A/G]TTATTACCATGTGCA	221687
rs775753153	in-del	-/G	1.7748e-05	0.00297887	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977084	GCCATTCTTCAACAA[-/G]ACCCACCTGGCATAA	221687
rs775833811	snp	A/G	1.64887e-05	0.00287125	synonymous-codon	RNF182	GRCh38.p7	6:13977461	GCTCACCCCCAAGAG[A/G]CTGGCCTCTCTGGTC	221687
rs775850117	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930284	ATGCCATGTTATACC[A/G]GGGACTTGAGCATCC	221687
rs775941300	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960774	CTACTTAAGTTTGAA[A/G]TTGTAGAAATGGTAC	221687
rs775941417	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13973394	TTGGTTTTGAGATGT[A/G]AGGACATGAGATTTG	221687
rs775954747	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13949525	TGCAAGAAAAAAGCA[A/G]TTGAGGGAATCTGTG	221687
rs776029410	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13961452	ATCTCGGTCTCCTGA[A/C]TCTAGATGCTATGTG	221687
rs776058083	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13959279	GACTTTGTACTGTTC[A/G]TGGAACTTAACAAAG	221687
rs776154191	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13947903	GACTTATGTAAATAG[A/C]TATATCACCATAAGT	221687
rs776209223	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13935630	ATCCAAAAAGATAGC[A/G]CATTAGTTATAACCA	221687
rs776327726	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13954323	AAATATTGGTATTCA[A/C]ATTTCCCTTATTGTC	221687
rs776328366	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13934412	CGTCGCTCACAGTTA[C/T]GTTAGTTGTTTTAAT	221687
rs776506798	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13943283	AGAGGTGGTTCCTGC[-/T]TTTTTTTTTTTTCTT	221687
rs776512846	snp	C/T	1.64849e-05	0.00287092	missense	RNF182	GRCh38.p7	6:13977451	CTGAGCTGCTGCTCA[C/T]CCCCAAGAGGCTGGC	221687
rs776600157	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13944335	TTCTCAGGTAGGCAT[A/G]TTAAGGAGGTGGTTT	221687
rs776614859	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13955538	ATAATGGCTTTTTAA[A/C]ATACTTGGTGTTTCA	221687
rs776620272	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13973469	ACCCAAATCTGACCT[G/T]ATATTGTAATAATCC	221687
rs776628164	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13943474	TTTCTTTTTTTAACA[C/G]TAAATCATGTATGCT	221687
rs776717772	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13930441	TTTGCATTGCCTCAC[A/G]GGGTTATCCTCAACC	221687
rs776729774	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13972235	GTGTGTACCCAGGAG[A/G]TGGAACTTGCAGTGA	221687
rs776827542	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971513	GAGTGGGGTACTGCT[A/G]TAAGGATACCTGAAA	221687
rs776908473	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942390	TCTGTGGCCCAGGCT[A/G]GAGTCAAGTGGTGTG	221687
rs776989099	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13961605	TTATTCCTGAACATT[A/T]ATTGGTTTAAAACTG	221687
rs777075059	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962367	TATCAATAGCTGAGC[A/G]TAAAAACCAATGTTC	221687
rs777077024	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950942	GCTGGGACTACAGTC[A/G]TGTGCCACCACACCT	221687
rs777165019	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13952106	GATAGTAAAGAGACA[A/G]GAGAGAGAGAGAGGA	221687
rs777174455	snp	A/G	1.64743e-05	0.00287	missense	RNF182	GRCh38.p7	6:13977759	GTCACCCTTGGGGTC[A/G]TCTTTGTCAGCCTGG	221687
rs777260729	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951738	GTCTTGCTTGTTGCC[C/T]CATAGCTGTGGGGTC	221687
rs777271786	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961329	CCATATAGTGCTTAT[A/G]TATGTAAAGTATTTA	221687
rs777294696	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13967331	AAAAGAGGCAGAGTT[G/T]ATGAAGAAAATAAAG	221687
rs777332821	in-del	-/GG			intron-variant	RNF182	GRCh38.p7	6:13939734	ATTTTTAGTAGAGAT[-/GG]GGTTTCACCTTGTTA	221687
rs777355500	snp	A/G			splice-donor-variant, intron-variant	RNF182	GRCh38.p7	6:13974365	GGCCTTGGAATTAGA[A/G]TAGGTATATTTTTTA	221687
rs777558261	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938965	GTTCACGCCTGTAAT[C/T]CCAGCTACTTGGGTG	221687
rs777685003	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13940356	TAATAAATCCAACTG[A/T]TGTGCTATTATTTTA	221687
rs777833707	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13957344	CTATTGAGAAAAGCC[A/G]CTGAGGGCAAATAAA	221687
rs777872691	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13976272	CTTTAATGAATGTAT[A/G]TGCACAGCTGTGGTT	221687
rs777921701	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13947450	AATTTTAGTCTTATT[A/G]TATGTGGCCTGGTTA	221687
rs777937341	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13964402	TGCCAATGTTCTGCC[A/C]AAATTAAACTTTTAT	221687
rs777959268	snp	C/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13977970	GATTAGTATCCATGA[C/G]ATTAACAAAACCCTT	221687
rs778005085	in-del	-/GTT			intron-variant, cds-indel	RNF182	GRCh38.p7	6:13925310	GGGAGCTGCCCCTCT[-/GTT]GTTGTTGTTATTTTC	221687
rs778015953	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13933945	ATCGCTTGAACCTGG[C/G]AGGCAGTGGTTGCAG	221687
rs778023826	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13953969	CCATGAGCACAGATG[C/T]TGGAAAGTAGAGAGA	221687
rs778130296	snp	C/T			synonymous-codon	RNF182	GRCh38.p7	6:13977752	TAAGAAAGTCACCCT[C/T]GGGGTCGTCTTTGTC	221687
rs778131916	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13949299	CTGTCAGAAACCTGA[A/C]ATGTGGGCATCCTGC	221687
rs778222423	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13965292	TCTGAAAGTACAGAA[A/C]AAAAATATAAAGGAA	221687
rs778237357	in-del	-/TGAGAT			intron-variant	RNF182	GRCh38.p7	6:13936414	GGATAATATCTCTAC[-/TGAGAT]TCAATTATTCTTTGG	221687
rs778314160	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13955137	TTTTGGCTTTGAGGG[A/C]CAATATGGTCTCTGT	221687
rs778390480	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13941779	GTATTTTAATCCTTC[C/T]GTGATGGTGTAGTGT	221687
rs778418771	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951998	CATCTTTGATCCACT[C/T]AAAGTGGGGTGGGAT	221687
rs778480317	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942729	TAGAAGTACAATTTT[A/G]TATCCTTTAGACTCT	221687
rs778498795	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13963280	AAGTTCATAAAAGAG[A/T]CTTCTAGGTAGGCAT	221687
rs778595405	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13926596	ATACTCTTTCATGAC[A/G]GTAATAAAATCGTAC	221687
rs778600254	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971508	ACCAGGAGTGGGGTA[C/T]TGCTATAAGGATACC	221687
rs778614174	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13936608	CTCAAAGATGAACAA[A/G]TCAGGTATAGCCCTA	221687
rs778649444	snp	A/G	3.29674e-05	0.00405988	missense	RNF182	GRCh38.p7	6:13977435	CTGCCAGAGAACCCT[A/G]CTGAGCTGCTGCTCA	221687
rs778687519	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13927742	TCAACATTCTCTTGC[A/C]ATTTCTAGTTGCACT	221687
rs778693944	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13959848	TGGAGGTACTGTAAG[A/C]CCTCTGGAACTCAGA	221687
rs778990463	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13925569	CCTTTTTTTCTTTGG[A/G]AGGTGCAGTTGCACC	221687
rs779057817	snp	C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13922596	TCATTATTTTAACCT[C/T]ATTTCAAAAATGGTG	221687
rs779084870	snp	A/G			utr-variant-3-prime	RNF182	GRCh38.p7	6:13979437	AGTGCGCCCATTCCA[A/G]CTGGAATAGCAGTTT	221687
rs779091302	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13927539	CACCATAGCTGTATT[C/T]TACCTGAAAGAATTC	221687
rs779158539	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13942951	CATTGTAGGTGTAGC[A/G]TTCAATGATCTTAGT	221687
rs779238676	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13936289	AAAATTTAATGTTTT[A/C]CCTTTCCCTATCTGT	221687
rs779246476	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13930075	TATCTGCAGGTTCCA[C/T]ATCTGCAGATTCTAT	221687
rs779433138	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13950872	TGCAATCTCAGCTCA[C/G]TGCAATCTCTGGCTC	221687
rs779441402	in-del	-/T			intron-variant	RNF182	GRCh38.p7	6:13966680	AGGCGGGAAGATTGC[-/T]TGACCCCGCGGGGTG	221687
rs779444894	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943870	AAGGTACTAAAAGAC[A/G]TTAAGGGTGATTTGT	221687
rs779446983	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	RNF182	GRCh38.p7	6:13977197	AATCTGTTACAATCG[A/G]TACAATCTGAAACAG	221687
rs779530863	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13927851	GATGGTAGTTTTTAA[A/T]TGATTTCTTCATTAC	221687
rs779534474	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13931392	AGCAACATGCTTTTT[A/G]CTACAGTGGGAGATT	221687
rs779578742	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13970830	TTGATCCAAAATACG[C/T]GTTGGCAGAAAAATA	221687
rs779667097	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13971628	AGTTTGGAACTTCCT[A/G]GAGTCTTGGAGGGCT	221687
rs779720588	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13941030	TGAATAGACTATACA[A/G]TATAATCAATCTGTA	221687
rs779756379	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13964827	TCCACAAGAGACCAA[A/G]GAGAAAAATCCATAG	221687
rs779802905	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13929710	TATGATCACTTTCTG[C/T]TACGTTAACCCAAAG	221687
rs779821576	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13950157	ATTACATATGTTACA[A/G]TGTTAACTCGTAGCA	221687
rs779844661	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13961067	ATATTATTTGTTGGC[A/G]TTCCATATAGATAAT	221687
rs779938553	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13965743	ACAGAAAGCCAATCA[C/T]GAGACGATGAGTATT	221687
rs780020551	in-del	-/TTG			intron-variant	RNF182	GRCh38.p7	6:13969108	TGTCTCTGTTTTTTG[-/TTG]TTGTTGTTGTTGTTG	221687
rs780031797	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13962186	CTCTAACTAGAATCC[A/G]GCTTCTGAATCTCTA	221687
rs780059345	in-del	-/ATGG			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923767	TTCAAATGGCAATAA[-/ATGG]CATTGTTCTGCTTTG	221687
rs780202772	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13936407	GAACTCAGGATAATA[C/T]CTCTACTGAGATTCA	221687
rs780224041	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956230	TTGGCTATTGGCTAT[C/T]GTAATAGTGACCAGC	221687
rs780224814	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956571	CTCAGGTGATCCACC[C/T]GTCTTGGCCTCCCAG	221687
rs780225544	snp	A/G	1.64762e-05	0.00287016	missense	RNF182	GRCh38.p7	6:13977619	CCACTGTGTCACACA[A/G]CTGGACTGTGTGGAA	221687
rs780287533	snp	A/C/T			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923283	GATCACCCACACATA[A/C/T]GGTTCTGAGCCCCCC	221687
rs780299895	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13931531	CTGGAATTCCTGGTG[A/C]ATACTTTCCTTGATA	221687
rs780323715	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13944101	GAGGTATCTCTCTGG[A/G]TGTTTACATTTCAAA	221687
rs780338162	snp	C/G	1.76899e-05	0.00297399	utr-variant-5-prime	RNF182	GRCh38.p7	6:13977090	CTTCAACAAGACCCA[C/G]CTGGCATAAGATTGC	221687
rs780371328	snp	C/G			upstream-variant-2KB, intron-variant	RNF182	GRCh38.p7	6:13924627	ATGGTGGTGCGACGG[C/G]AGTTGGAATGTCCAG	221687
rs780404907	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13941075	ATTTGGTGCACATAG[A/C]TTGGGTCAAATTCAT	221687
rs780413481	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13945357	TGAAACTGCCACTTC[A/G]TTGCCAGGGCATTCT	221687
rs780510044	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13975608	TTAAAAATTAAAGTC[C/T]TAAAATGAAGATAAT	221687
rs780599818	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13972108	GATCAAGACCATCCT[A/G]GCTAACACGGTGAAA	221687
rs780602180	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13974622	CCCAACATAAAGTGT[A/T]ACTGCTACTCTTCTA	221687
rs780697262	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13971702	TTTGAATGCCTTTGA[C/T]CAAAATGCTGATAGT	221687
rs780715843	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13960392	TATATCTGTAATCCC[A/C]GCACGTTGGGAGGCC	221687
rs780787899	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	RNF182	GRCh38.p7	6:13977204	TACAATCGATACAAT[C/T]TGAAACAGAGGAAAC	221687
rs780803734	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13961284	AGTACCATATCAATG[G/T]ATCCATTATTTCTAA	221687
rs780852971	in-del	-/TGCC			intron-variant	RNF182	GRCh38.p7	6:13944956	AAGCTGCTTACTAAG[-/TGCC]TGCCTGATCCTAAGA	221687
rs780887440	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13938308	AGGCGTGAGCCACTG[C/T]GCCTGGCCTTTTTCT	221687
rs780948149	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13937535	TTGGTATAGTATTTC[A/G]TTGCTGCCTGTAGCA	221687
rs780981648	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13951518	AGAGTATTCCTCCCT[C/T]ATAGCTGCCATTAGC	221687
rs781062724	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13956465	TAGTAGCTGGGATTA[C/T]AGATGCATGCCACCA	221687
rs781078578	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13928425	TAGGATTATTTATTT[C/T]ATATGTAATTCTTAA	221687
rs781140706	snp	A/C			upstream-variant-2KB	RNF182	GRCh38.p7	6:13923371	TGGATGCATAGTATT[A/C]CATGGTATGAAGTGC	221687
rs781214947	snp	A/G/T	3.29654e-05	0.00405978	synonymous-codon	RNF182	GRCh38.p7	6:13977527	AACCATCATGGAGGT[A/G/T]CAGAGAGAGAGCTCC	221687
rs781324965	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13947262	TAAATTGCAGAAAAA[A/C]CTCAAAAACAATGGA	221687
rs781358814	snp	C/G			intron-variant	RNF182	GRCh38.p7	6:13957175	TTTCCTAGCAATCTT[C/G]TTTTTATGTAAGTAT	221687
rs781440830	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13945754	GTGCCTTAATTTCAT[C/T]TTGACAGTTTTCCTC	221687
rs781449124	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13932638	AAATTAATATTGTAT[A/G]GACATAGTCAAATAC	221687
rs781537355	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13933827	GTTCGAGACCAACCT[G/T]GCCAATGTGGTGAAA	221687
rs781549068	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967988	GCCAGTGGAAACACT[A/G]TAGTCTTTAGCTATT	221687
rs781655219	snp	A/G			upstream-variant-2KB	RNF182	GRCh38.p7	6:13924149	CCTTGGCACAGAGTC[A/G]CTCAGGGCTCATGGT	221687
rs781664278	snp	A/G	6.88409e-05	0.00586649	utr-variant-3-prime	RNF182	GRCh38.p7	6:13977897	AATTGGACACACATT[A/G]CCCTGTTTGAGTGTG	221687
rs781688423	in-del	-/GCAACG			intron-variant	RNF182	GRCh38.p7	6:13930131	AAATATTTGGAAAAT[-/GCAACG]ATTCCAAAAAATAAT	221687
rs781758064	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13952710	TTCTCAGATATTGCA[C/T]AGGAAACAATTTGAG	221687
rs796118146	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13929635	ATCAACTCATTTAAT[C/T]CTCACAACAACCCTT	221687
rs796118796	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13954361	TTCTCCCCTTCCCCA[C/T]TGGTTGGTTAGAATT	221687
rs796119323	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13940304	TCAATATGGTAATCA[C/T]ATTTTAAAAAAATGT	221687
rs796144159	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13941725	GTTATCCTAGAGATT[A/T]TAACATCTATTTTTC	221687
rs796186450	in-del	-/A			intron-variant	RNF182	GRCh38.p7	6:13939516	TACATTTTTGTTTTT[-/A]TTTTTTTATTTTGTA	221687
rs796274435	snp	G/T			intron-variant	RNF182	GRCh38.p7	6:13939259	AACCTGATAGATTTT[G/T]ATTGGAATTGCATTG	221687
rs796376908	in-del	G/TT			intron-variant	RNF182	GRCh38.p7	6:13926793	GTGTGTGTGTGTGTT[G/TT]TTTTTTTTTCCTGAG	221687
rs796428681	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13971487	CAACTAATACAGTAA[A/T]TTAGTACCAGGAGTG	221687
rs796536051	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13948980	ACTATTAATGTCAAA[C/T]CCAATTTTTAATAAA	221687
rs796582209	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13960370	AACTTGGCCAGGTGC[A/G]ATGGCTTATATCTGT	221687
rs796835616	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13967009	GCCTGGCTAATTTTT[A/G]TATGTTTTTGTAGAG	221687
rs796848091	multinucleotide-polymorphism	CA/TG			intron-variant	RNF182	GRCh38.p7	6:13948157	AATATTTATGAATAC[CA/TG]TAGTTTTCCAAGAGT	221687

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