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

RNF152

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1133216	snp	A/G	0.470424	0.117954	intron-variant	RNF152	GRCh38.p7	18:61886127	TGACCAGGCTGCAGT[A/G]CGTATACCAATGTTT	220441
rs1135529	snp	C/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808353	AGATAAATGAGCTGC[C/T]GGGCTGTGTAGAAAA	220441
rs1142939	snp	C/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815385	Ctttatttttttttt[C/T]tttttattGAAACCC	220441
rs4072460	snp	A/G	0.433673	0.1696	intron-variant	RNF152	GRCh38.p7	18:61867925	TAAATTTACATAATA[A/G]TAAAGTTGTATTTTT	220441
rs4073064	snp	A/G	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61865494	AACCAGGTTTGTCAC[A/G]TGGATTAGTAATTTA	220441
rs4075336	snp	C/T	0.34659	0.230587	intron-variant	RNF152	GRCh38.p7	18:61867335	CATGCTCCTGTAGTC[C/T]CAGCTACTCGGGAGG	220441
rs4076952	snp	C/G/T	0.251014	0.249998	intron-variant	RNF152	GRCh38.p7	18:61829504	GAGAGGGGAGAGAGA[C/G/T]ATATATATATATCAG	220441
rs4078129	snp	C/T	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61884637	AATCTCAGCTCACTG[C/T]AACCTCCACCTCTCA	220441
rs4083955	snp	A/T	0.482979	0.0906686	intron-variant	RNF152	GRCh38.p7	18:61838564	CTAGAATGAACAGTC[A/T]TCATTCCTCTGAAGT	220441
rs4129490	snp	C/T	0.474992	0.108989	intron-variant	RNF152	GRCh38.p7	18:61833955	TCCTTTAATTATGTG[C/T]GGTTAGCAAAAGCTA	220441
rs4129491	snp	C/T	0.474903	0.109173	intron-variant	RNF152	GRCh38.p7	18:61834114	ATCTTATTTTTGTTA[C/T]GTCCTGGCTTGAATC	220441
rs4131216	snp	C/T	0.48692	0.0798058	intron-variant	RNF152	GRCh38.p7	18:61838115	TTGGGAATTGTTTCA[C/T]AGGGACTGATAAAGG	220441
rs4131217	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61838062	AACCTCTACCTTTGT[A/G]TGTGGGGACGGGAAG	220441
rs4280353	snp	C/T	0.480775	0.0961398	intron-variant	RNF152	GRCh38.p7	18:61847750	CCGGTCTCCCTCCCA[C/T]CCACTTCCCAAACCT	220441
rs4293482	snp	C/T	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61884906	GCCTAATAAGTGGTT[C/T]AAATACCTGATGCTC	220441
rs4294914	snp	A/G	0.482309	0.0923707	intron-variant	RNF152	GRCh38.p7	18:61841642	CCTCTACCTCTGAGT[A/G]GGTAGAGATGCAGAA	220441
rs4297789	snp	A/C	0.486984	0.079614	intron-variant	RNF152	GRCh38.p7	18:61837327	TGGGGAAAATGCCCA[A/C]AGTGATACAAGGCAT	220441
rs4319862	snp	G/T	0.331874	0.236213	intron-variant	RNF152	GRCh38.p7	18:61826101	CAAGGAATGAGCAAG[G/T]CTATGTTCTGTGGGG	220441
rs4358044	snp	G/T	0.431325	0.172108	intron-variant	RNF152	GRCh38.p7	18:61880545	TAAAGCACTTTAAAC[G/T]GAAAGCACCCAAGCG	220441
rs4362478	snp	A/G	0.0901274	0.1922	synonymous-codon	RNF152	GRCh38.p7	18:61816077	GGTCACCACGGTGAC[A/G]GACTTCTGCTGGCTC	220441
rs4381693	snp	C/T	0.482234	0.0925596	intron-variant	RNF152	GRCh38.p7	18:61841947	CAGCCATTGACAATA[C/T]GTAACAAATGGACAT	220441
rs4389228	snp	C/T	0.42666	0.176893	intron-variant	RNF152	GRCh38.p7	18:61841922	TCAACTCTACCACTG[C/T]AACAGAAAGCAGCCA	220441
rs4398187	snp	C/T	0.021333	0.101051	intron-variant	RNF152	GRCh38.p7	18:61833899	TAAAAAAAAAAGTTT[C/T]ATCCACAAGATAAAA	220441
rs4398188	snp	C/T	0.27008	0.249192	intron-variant	RNF152	GRCh38.p7	18:61862195	TCCATCCTGACCCCC[C/T]TATCTCCTCTCTGCC	220441
rs4424997	snp	C/T	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61837426	GATTATGTAAGAGAA[C/T]GTCCTTATTATCAGG	220441
rs4432347	snp	G/T	0.205723	0.246048	intron-variant	RNF152	GRCh38.p7	18:61825836	ACATTTTAATAAAAT[G/T]AACTACACATGTTCC	220441
rs4445995	snp	A/T	0.427119	0.176434	intron-variant	RNF152	GRCh38.p7	18:61841575	TAGTCTAGGGATTCT[A/T]AACTTTGGGGGGTTA	220441
rs4459645	snp	A/G	0.482309	0.0923707	intron-variant	RNF152	GRCh38.p7	18:61841471	TGAATAAATGAACTT[A/G]AGCTGGATCTATTTT	220441
rs4473290	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61844798	ATTTATCAAGGGAAG[A/G]TGCAAAATGCATTTT	220441
rs4476269	snp	C/T	0.474903	0.109173	intron-variant	RNF152	GRCh38.p7	18:61832747	GCCAGCAAATAAAAT[C/T]GACAGGATTTTAAAA	220441
rs4517883	snp	A/T	0.475525	0.107882	intron-variant	RNF152	GRCh38.p7	18:61888323	GAGTCAATTAGAAAT[A/T]GAAAATCCCTAAGCA	220441
rs4520933	snp	C/T	0.497722	0.0336691	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813848	GTCAGACATGCATTA[C/T]GGCAGCCTGGGAGAG	220441
rs4538107	snp	C/G	0.0891305	0.191366	synonymous-codon	RNF152	GRCh38.p7	18:61815969	GCACACCCCCGACCA[C/G]GTGGAGCTTTTCACC	220441
rs4550566	snp	A/G	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61827536	TCCTCAAATTACCCA[A/G]AGAACATTCTATATT	220441
rs4555248	snp	A/G	0.340784	0.232934	intron-variant	RNF152	GRCh38.p7	18:61834519	TGATGGACTCTATTG[A/G]CCTTTATTTACCTTC	220441
rs4616381	snp	C/T	0.487746	0.0773096	intron-variant	RNF152	GRCh38.p7	18:61824944	AAAGATGCTGACAGA[C/T]AGACAGACAGGCAGG	220441
rs4940528	snp	G/T	0.487241	0.0788465	intron-variant	RNF152	GRCh38.p7	18:61818021	CACTCCTTCACATTT[G/T]TCTTAAAAGTGACCC	220441
rs4940529	snp	C/T	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61830114	gcaaccttcacttca[C/T]gggttccagggattc	220441
rs4940530	snp	C/T	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61830146	cctgcctcagactcc[C/T]gggtagctgggacta	220441
rs4940531	snp	G/T	0.49121	0.0657086	intron-variant	RNF152	GRCh38.p7	18:61852256	AGTCTCAAGGGACTT[G/T]CCCATTTGAGGAAAA	220441
rs4940532	snp	C/T	0.273856	0.248859	intron-variant	RNF152	GRCh38.p7	18:61852553	AAAAGAACATCTAGA[C/T]TGTCAGTCTTCAAAG	220441
rs4940533	snp	A/G	0.431769	0.17164	intron-variant	RNF152	GRCh38.p7	18:61860558	gctgccggttgcata[A/G]gagtctagcacacac	220441
rs4940534	snp	A/G	0.442791	0.15916	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868195	TTCGGGTGTTGCTGT[A/G]GACTTACAGCATATA	220441
rs4941060	snp	A/T	0.335101	0.23507	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810026	TGCCCCACCTGCTTA[A/T]GTTCTTCAATGATTA	220441
rs4941061	snp	A/C	0.0633504	0.166319	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810243	AACAGTTTTTTACTG[A/C]ATTTTAACTCCAATT	220441
rs4941062	snp	A/G	0.481087	0.0953875	intron-variant	RNF152	GRCh38.p7	18:61817851	TCCACTGGCATTTCA[A/G]TAAGGGCTGCCTGAC	220441
rs4941063	snp	A/C	0.0581099	0.160244	intron-variant	RNF152	GRCh38.p7	18:61817874	TGCCTGACTCAGTTT[A/C]CCATTGAAAGCATCC	220441
rs4941064	snp	A/C	0	0	intron-variant	RNF152	GRCh38.p7	18:61820330	AGAGACTCCGTCTCA[A/C]CAAAAAAAAAAAAAA	220441
rs4941065	snp	A/G	0.0626037	0.165477	intron-variant	RNF152	GRCh38.p7	18:61823488	ATTTTTAGTAGAGAT[A/G]GGGTTTCGCCATATT	220441
rs4941066	snp	C/G	0.417359	0.185718	intron-variant	RNF152	GRCh38.p7	18:61833028	ATACATTAATTCAGT[C/G]ACTGTGCCAGTTAAG	220441
rs4941067	snp	C/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833076	CTTCCATTCCTCAGC[C/T]GTATCTACTAAAATT	220441
rs4941068	snp	A/C	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833408	AAAGAATCCAAATTT[A/C]AGGTGATTCACAATG	220441
rs4941069	snp	A/G	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833514	TCGAAACTCCTCTGC[A/G]TTTCCCTCTAATGGA	220441
rs4941070	snp	A/C	0.0718919	0.175435	intron-variant	RNF152	GRCh38.p7	18:61838326	AGACTCCTCTTTTGG[A/C]TTTTCATTTGCTTTG	220441
rs4941071	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61861312	acaatatttttattg[C/T]atctcttccatgttt	220441
rs4941072	snp	A/G	0.121369	0.214369	intron-variant	RNF152	GRCh38.p7	18:61866687	GCTGTGTGCTCCTAC[A/G]GTGACATGTTCATCC	220441
rs4941073	snp	C/G	0.42803	0.175514	intron-variant	RNF152	GRCh38.p7	18:61870879	ATCACACACATTGCA[C/G]CCATGATTCCATCCC	220441
rs4941074	snp	A/C	0.440609	0.161766	intron-variant	RNF152	GRCh38.p7	18:61870880	TCACACACATTGCAC[A/C]CATGATTCCATCCCC	220441
rs4941075	snp	A/G	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61875135	AGAGTTTGAATAGAA[A/G]GATAGAGGAAGAAAG	220441
rs4941076	snp	C/T	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61879521	CTATGCTGTGTTTTG[C/T]GGGAGGGCAGAGAGG	220441
rs4941077	snp	A/G	0.0626037	0.165477	intron-variant	RNF152	GRCh38.p7	18:61879561	GAGAAAGCGTGTTCC[A/G]GGGAAAGGGAACTAC	220441
rs4941078	snp	A/G	0.477004	0.104734	intron-variant	RNF152	GRCh38.p7	18:61879793	ACACGGAGAAACCCC[A/G]TCTCTACTGAAAAAA	220441
rs4941079	snp	G/T	0.470618	0.117591	intron-variant	RNF152	GRCh38.p7	18:61879992	AAAAATTTTTTTTGT[G/T]CACAGCTTTTTAGTA	220441
rs4941080	snp	A/G	0.470521	0.117772	intron-variant	RNF152	GRCh38.p7	18:61886641	GCAGGTCCAGGGTGA[A/G]TGATAACTGGAAGGG	220441
rs4941081	snp	A/G	0.483199	0.0901004	intron-variant	RNF152	GRCh38.p7	18:61890690	TAATATGGAAAAGCA[A/G]CATTTGTTTCAAAAT	220441
rs4941082	snp	C/T	0.492087	0.0623997	intron-variant	RNF152	GRCh38.p7	18:61890819	AATGACCCTCAACAA[C/T]GTAAGGACCGAACTG	220441
rs4941083	snp	C/T	0.483491	0.0893421	intron-variant	RNF152	GRCh38.p7	18:61890827	TCAACAATGTAAGGA[C/T]CGAACTGTATGGAAT	220441
rs5016055	snp	G/T	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61827597	CCAGTGGGTTTTATA[G/T]ATATCTCTTTAAGTA	220441
rs5825462	in-del	-/ATAT			intron-variant	RNF152	GRCh38.p7	18:61827601	GGGTTTTATAGATAT[-/ATAT]CTCTTTAAGTAAGTC	220441
rs5825463	in-del	-/A	0.475702	0.107512	intron-variant	RNF152	GRCh38.p7	18:61833885	TGCCATTTGAGCTTT[-/A]AAAAAAAAAGTTTCA	220441
rs5825464	in-del	-/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61834680	ACTGAAATTAGGCCA[-/T]TTTTAAAAAAAATTA	220441
rs5825466	in-del	-/AC	0.327445	0.237702	intron-variant	RNF152	GRCh38.p7	18:61838018	CAGTCTTTTGAAGAA[-/AC]ACACACATGGTTCCT	220441
rs5825467	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61838025	TTGAAGAAACACACA[-/CA]TGGTTCCTCTGACTT	220441
rs6567245	snp	C/T	0.495999	0.0445491	intron-variant	RNF152	GRCh38.p7	18:61828295	TTGCCCAAGCTAGTA[C/T]GGTGACTATTCACAA	220441
rs6567246	snp	C/G	0.404733	0.196361	intron-variant	RNF152	GRCh38.p7	18:61828373	CTTCCTGCCTTAGCC[C/G]CCCGAGTAGCTGGGA	220441
rs6567248	snp	A/G	0.349671	0.229272	intron-variant	RNF152	GRCh38.p7	18:61883209	ATGCAGCTTTCAAAA[A/G]TATTTCTGAAGAATA	220441
rs7227060	snp	A/G	0.476918	0.104919	intron-variant	RNF152	GRCh38.p7	18:61865417	GAGAATTTGAAAGGA[A/G]ATTGCTTCCAGGATA	220441
rs7228799	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61851938	ACGACATCTGCACAG[A/T]ACCTTGTGGCTCATT	220441
rs7229409	snp	C/T	0.427423	0.176128	intron-variant	RNF152	GRCh38.p7	18:61840405	TCTATCTTTTCTTTA[C/T]AACCCAGAACCCCAA	220441
rs7229834	snp	C/T	0.48955	0.071525	intron-variant	RNF152	GRCh38.p7	18:61853127	TTtattagtttccta[C/T]tgccactgtaacaaa	220441
rs7230629	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61844873	GGCCTTTTAAAACAA[A/C]AAAAAAAAAGCATTT	220441
rs7230956	snp	A/G	0.322245	0.239334	intron-variant	RNF152	GRCh38.p7	18:61857028	AAGTAGTAAAACAAG[A/G]AGAAACCAGCATTAT	220441
rs7231456	snp	A/G	0.320814	0.239761	intron-variant	RNF152	GRCh38.p7	18:61857410	CAAATATTTTGCCTT[A/G]GAACTGCTTTAGAAC	220441
rs7232949	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61857575	AATTTTTCTTCAAAC[C/T]TACTGTTACTTCCTT	220441
rs7233207	snp	C/T	0.430732	0.172731	intron-variant	RNF152	GRCh38.p7	18:61843967	attttatgttatgtg[C/T]attttaccacagtaa	220441
rs7234737	snp	C/G	0.406123	0.195258	intron-variant	RNF152	GRCh38.p7	18:61826238	AAAGCAGAAACTTCT[C/G]AGAAATGAGAACTGC	220441
rs7235368	snp	A/G	0.406123	0.195258	intron-variant	RNF152	GRCh38.p7	18:61826272	AAATACCTTCTTTAG[A/G]GCAGGTCTATTTCCA	220441
rs7236480	snp	A/G	0.450231	0.149691	intron-variant	RNF152	GRCh38.p7	18:61842474	CGAGTTGTCACAGGG[A/G]CTTTGTTTCCCTGGA	220441
rs7237239	snp	A/G	0.179105	0.239737	intron-variant	RNF152	GRCh38.p7	18:61871989	gactgggtaatttat[A/G]aagaaaagaggctta	220441
rs7237854	snp	A/G	0.480302	0.0972668	intron-variant	RNF152	GRCh38.p7	18:61839756	AAAAAATTGCTGGGC[A/G]TGGTGGTGGGTGCCT	220441
rs7238578	snp	C/T	0.0711525	0.174681	intron-variant	RNF152	GRCh38.p7	18:61875022	CCATCCCCTGGGATA[C/T]GCCATGGTCTGCAAG	220441
rs7238823	snp	C/T	0.419135	0.184101	intron-variant	RNF152	GRCh38.p7	18:61839714	TCCTGGCTAACACAG[C/T]GACACCCTGTCTCTA	220441
rs7240831	snp	G/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61835612	tcaaaaataataaat[G/T]aaaaaggataaacaa	220441
rs7241508	snp	A/T	0.230896	0.249269	intron-variant	RNF152	GRCh38.p7	18:61872118	aaatgggaacaggca[A/T]cttacatggcaggac	220441
rs7242295	snp	C/T	0.254385	0.249962	intron-variant	RNF152	GRCh38.p7	18:61823273	TGATGAAGCAAAGAA[C/T]CCAGAAAGTGAAAAT	220441
rs7243378	snp	C/T	0.0360663	0.129354	intron-variant	RNF152	GRCh38.p7	18:61817925	GAGCCATGATGACTC[C/T]AGAAAGAATTACTCA	220441
rs7244472	snp	A/G	0.334642	0.235236	intron-variant	RNF152	GRCh38.p7	18:61819842	cctagtcaacataac[A/G]agactctgtctctac	220441
rs7244703	snp	A/G	0.332799	0.23589	intron-variant	RNF152	GRCh38.p7	18:61828448	TTTTTTTGTAGAGAC[A/G]GGATCTTGCCATGTT	220441
rs7359752	snp	C/T	0.18134	0.240387	intron-variant	RNF152	GRCh38.p7	18:61861444	tagcctatatgtgta[C/T]tgggctacaccacct	220441
rs7505697	snp	A/G	0.48435	0.0870631	intron-variant	RNF152	GRCh38.p7	18:61888172	CCCTCACAACTCCAC[A/G]AAGAACGTAGTCCAG	220441
rs8085180	snp	A/C	0.483636	0.0889627	intron-variant	RNF152	GRCh38.p7	18:61890048	CCATGTTAGTAAATA[A/C]CATATCAACATATTA	220441
rs8085799	snp	A/G	0.0912534	0.193131	intron-variant	RNF152	GRCh38.p7	18:61853874	caaggatgaggacaa[A/G]gacttctctggggtc	220441
rs8085961	snp	A/C	0.493613	0.0561475	intron-variant	RNF152	GRCh38.p7	18:61840978	AGAAGCACCTGTCCA[A/C]CTGGGTAACACAAAA	220441
rs8086397	snp	A/G	0.483126	0.0902898	intron-variant	RNF152	GRCh38.p7	18:61890537	TGCAGCATGGGAAGG[A/G]AAGAAACTGTATTTA	220441
rs8087731	snp	A/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813280	CTCTCTCTCTCTCTC[A/T]CACACACACACACAC	220441
rs8087749	snp	C/T	0.338069	0.233974	intron-variant	RNF152	GRCh38.p7	18:61822120	GAAAATATATGAGAA[C/T]AATTTTTAAATGTCA	220441
rs8088862	snp	A/T	0.0456336	0.143994	intron-variant	RNF152	GRCh38.p7	18:61822501	TGACAAAGTGCGCGC[A/T]TTCATTTGGTAGGTG	220441
rs8090006	snp	A/G	0.479984	0.0980171	intron-variant	RNF152	GRCh38.p7	18:61844969	CATTTTATTCCTTCC[A/G]TTCCTCCTGAGGGCC	220441
rs8091174	snp	C/T	0.421051	0.182323	intron-variant	RNF152	GRCh38.p7	18:61826836	TCAAGCTCCAGAATG[C/T]AAACTGTTTTCAAAA	220441
rs8092069	snp	C/G	0.0275645	0.114116	intron-variant	RNF152	GRCh38.p7	18:61879299	attacatttgcatag[C/G]atttacattgtatta	220441
rs8092621	snp	A/C	0.0205511	0.0992634	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814683	GAGGAAACAGGAATT[A/C]TAACTGGCTTAACTC	220441
rs8093222	snp	A/G	0.340559	0.233022	intron-variant	RNF152	GRCh38.p7	18:61832679	CTAAAAAAACAGCCC[A/G]ATTTAACAGGCATGC	220441
rs8093878	snp	C/T	0.411746	0.190626	intron-variant	RNF152	GRCh38.p7	18:61845083	TTTGTTGGTGGGTGG[C/T]GGGTTTTTTGTTTGT	220441
rs8094305	snp	C/T	0.47517	0.10862	intron-variant	RNF152	GRCh38.p7	18:61832664	AATTCTACCTGTGAA[C/T]TAAAAAAACAGCCCG	220441
rs8095201	snp	A/T	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61826973	TGGCCATCATTTACC[A/T]TTATTGAGAACATAC	220441
rs8095322	snp	A/G	0.354665	0.227036	intron-variant	RNF152	GRCh38.p7	18:61827032	TTGAAATATGGATCT[A/G]TTATTTCAACAATAT	220441
rs8096049	snp	C/T	0.470327	0.118136	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894079	TAGGGGCGCAGACAT[C/T]CCTGCGCACCCCTCT	220441
rs8097540	snp	C/T	0.481856	0.0935034	intron-variant	RNF152	GRCh38.p7	18:61843327	ATTAGATATTAACAT[C/T]CTTCAGGATTGTTGG	220441
rs8097920	snp	A/G	0.0134861	0.0810011	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810710	CAGCAACTGAACATC[A/G]TTGCTTTTTAAATAG	220441
rs8099253	snp	C/T	0.334642	0.235236	intron-variant	RNF152	GRCh38.p7	18:61819331	GACCGTGGGCAGCCC[C/T]CAGTGCCAGGCCAAG	220441
rs9319985	snp	A/G	0.341449	0.232674	synonymous-codon	RNF152	GRCh38.p7	18:61816281	CACGGAGAAGCCGGG[A/G]GGCAGCTTGGTGACA	220441
rs9789123	snp	C/T	0.282895	0.247826	intron-variant	RNF152	GRCh38.p7	18:61866548	CCAGCAGGGCCTACG[C/T]ATCCTTTGGTGACTT	220441
rs9807754	snp	A/G	0.175897	0.238765	intron-variant	RNF152	GRCh38.p7	18:61859390	ACACACTGTTCCCAG[A/G]GCTCCCAACACATGC	220441
rs9944722	snp	C/T	0.470521	0.117772	intron-variant	RNF152	GRCh38.p7	18:61877692	TTTTCTGATAAAATA[C/T]AGAAATTACAAGAAT	220441
rs9944883	snp	A/C	0.474992	0.108989	intron-variant	RNF152	GRCh38.p7	18:61836928	gattacaggctttga[A/C]agacaggatatttac	220441
rs9945863	snp	C/T	0.494733	0.0510469	intron-variant	RNF152	GRCh38.p7	18:61850652	GGCTTTCAGTTTGGA[C/T]CATTTGCTATGAAAA	220441
rs9945922	snp	C/T	0.0225045	0.103662	intron-variant	RNF152	GRCh38.p7	18:61843510	ctacatccatgttca[C/T]agcaacattatttac	220441
rs9946444	snp	A/T	0.0236746	0.106192	intron-variant	RNF152	GRCh38.p7	18:61840503	CTTCACATTTTAGTC[A/T]GGAAACTCCTAGTTC	220441
rs9946472	snp	A/C	0.426047	0.177503	intron-variant	RNF152	GRCh38.p7	18:61881585	AGTCAAAGACATGAA[A/C]TCAAATGAATGCTGA	220441
rs9947081	snp	A/G	0.210605	0.246877	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811221	CAATTTTGAAACAAC[A/G]TAAGTTTTCAAATAA	220441
rs9947257	snp	A/G	0.49533	0.0480965	intron-variant	RNF152	GRCh38.p7	18:61848531	CACACAGCCCCCCAG[A/G]CTGTACGTGGCCTCA	220441
rs9949250	snp	C/T	0.244885	0.250961	intron-variant	RNF152	GRCh38.p7	18:61851787	ACTAGAGCCTCTACT[C/T]GGTCAATACCATAGG	220441
rs9949492	snp	A/G	0.392325	0.205532	intron-variant	RNF152	GRCh38.p7	18:61854433	AGCCTTAAAGGAAAC[A/G]CACAATAGGTAACAC	220441
rs9949601	snp	C/T	0.483995	0.0880135	intron-variant	RNF152	GRCh38.p7	18:61883967	AAACTCCCATGTAAA[C/T]GCTGAAGGCTGTAGT	220441
rs9950358	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61854552	TCTTTCTCAACTGAG[C/T]GAATTAAAGAGGGCT	220441
rs9951639	snp	C/T	0.43088	0.172575	intron-variant	RNF152	GRCh38.p7	18:61816969	CCAATAAGTTCATAG[C/T]ATTTCCTAGAAGTAA	220441
rs9952742	snp	C/T	0.339656	0.233371	intron-variant	RNF152	GRCh38.p7	18:61834988	TGATTCCAATGTCAA[C/T]TGAGGGTTGAGAGTC	220441
rs9952990	snp	A/G	0.489376	0.0721049	intron-variant	RNF152	GRCh38.p7	18:61885818	CCTTTAATTATAAAC[A/G]CAGGTGGGGCAGTCA	220441
rs9953081	snp	G/T	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61885887	ATCAATGCCTGCTCC[G/T]TTAGATTGTGGGGTG	220441
rs9953088	snp	A/G	0.489318	0.0722982	intron-variant	RNF152	GRCh38.p7	18:61885907	ATTGTGGGGTGGTCT[A/G]GTAGGCTGTAAAGTC	220441
rs9954003	snp	C/T	0.48435	0.0870631	intron-variant	RNF152	GRCh38.p7	18:61888104	ATGCAGGCATTAGTA[C/T]ATCAAGGGGTAAATA	220441
rs9955483	snp	C/T	0.11228	0.208646	intron-variant	RNF152	GRCh38.p7	18:61840879	ATTTCAGAGCCTTTT[C/T]CCCTTCCCTACCCAT	220441
rs9956924	snp	A/G	0.489434	0.0719116	intron-variant	RNF152	GRCh38.p7	18:61881592	GACATGAAATCAAAT[A/G]AATGCTGAAGCAACT	220441
rs9957116	snp	G/T	0.484066	0.0878235	intron-variant	RNF152	GRCh38.p7	18:61881742	TGCCCCCAAGAGAAT[G/T]TTATTTTAAGGAGCA	220441
rs9957629	snp	A/C	0.484066	0.0878235	intron-variant	RNF152	GRCh38.p7	18:61881567	ACTGTTGCCCTTTGC[A/C]ATAGTCAAAGACATG	220441
rs9958268	snp	A/T	0.348574	0.229746	intron-variant	RNF152	GRCh38.p7	18:61882833	GGAATCTTTGGAAAG[A/T]AAACACTGGGTGCTG	220441
rs9958401	snp	C/G	0.482309	0.0923707	intron-variant	RNF152	GRCh38.p7	18:61891982	GACTCTGCCCTCTAG[C/G]AGAAAATGCTAATGC	220441
rs9959429	snp	A/G	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61848195	GCTAACTAAAACCCT[A/G]TGAGGTAGCAGGAAG	220441
rs9960476	snp	C/G	0.413914	0.188765	intron-variant	RNF152	GRCh38.p7	18:61817131	GGGTTAGGATTGTTC[C/G]TCTTCACAGAGAAGT	220441
rs9961592	snp	C/T	0.474723	0.109542	intron-variant	RNF152	GRCh38.p7	18:61835166	CAGCAAAAGTATTTG[C/T]AAGTATTCATTCTGA	220441
rs9962045	snp	C/G	0.0577344	0.159793	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893325	ACAGCGCGGCAATCC[C/G]GAGCATCTTTCTTTC	220441
rs9962876	snp	A/G	0.0718919	0.175435	intron-variant	RNF152	GRCh38.p7	18:61842029	tgaccccagggctat[A/G]CTAAAAGGTATCACT	220441
rs9962890	snp	A/T	0.0707826	0.174302	intron-variant	RNF152	GRCh38.p7	18:61842053	TATCACTTTAAAGCC[A/T]GCACAAGGAATCTAA	220441
rs9963722	snp	A/G	0.33693	0.2344	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809236	CTACTTAATAGTTGC[A/G]TTGTCCCTCAACCCA	220441
rs9963954	snp	C/G	0.478354	0.101757	intron-variant	RNF152	GRCh38.p7	18:61845928	CTTTGTGTGGGGGGG[C/G]GTGGTGATGAGGACT	220441
rs9965497	snp	C/G	0.370974	0.218781	intron-variant	RNF152	GRCh38.p7	18:61871707	AGGCTGGGCTTTGGA[C/G]CATGAACAGCCTGGC	220441
rs9966069	snp	C/T	0.210301	0.246828	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809202	TGCTTCATGTCTCCC[C/T]TTCCCTCTCCCTCTC	220441
rs9966870	snp	C/G	0.463234	0.130503	intron-variant	RNF152	GRCh38.p7	18:61818989	AAAAATCTGGATTAT[C/G]GAATTAGACACAAAA	220441
rs9973181	snp	A/G	0.340108	0.233197	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61815050	GACACACACACATAC[A/G]CACACAAATACACAA	220441
rs10782066	snp	A/G	0.414741	0.188044	intron-variant	RNF152	GRCh38.p7	18:61839684	GCGGATCACAAGGTC[A/G]GGAGATCGAGATCAT	220441
rs10871795	snp	A/G	0.285257	0.247501	intron-variant	RNF152	GRCh38.p7	18:61839671	GAGGCTGAGGCGGGC[A/G]GATCACAAGGTCGGG	220441
rs11152315	snp	A/T	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813278	CTCTCTCTCTCTCTc[A/T]cacacacacacacac	220441
rs11152316	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839667	TTGGGAGGCTGAGGC[A/G]GGCGGATCACAAGGT	220441
rs11152317	snp	A/G	0.274393	0.248807	intron-variant	RNF152	GRCh38.p7	18:61856209	TCTAATTGAGTTGGT[A/G]AGTAAAGCGATGACA	220441
rs11152318	snp	A/G	0.485664	0.0834419	intron-variant	RNF152	GRCh38.p7	18:61875776	TCTGAAATGTCTCTT[A/G]CATTGATTCACCCTC	220441
rs11152319	snp	C/T	0.485664	0.0834419	intron-variant	RNF152	GRCh38.p7	18:61875787	TCTTGCATTGATTCA[C/T]CCTCCCATTCCTGCC	220441
rs11290555	in-del	-/A	0.484066	0.0878235	intron-variant	RNF152	GRCh38.p7	18:61891436	TTTATTCTTTCTATT[-/A]AAAAAAAAACCACAC	220441
rs11341958	in-del	-/A	0.494057	0.0541878	intron-variant	RNF152	GRCh38.p7	18:61879981	GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	220441
rs11432214	in-del	-/G	0.0170251	0.090679	intron-variant	RNF152	GRCh38.p7	18:61866455	CACATCCACACTCTC[-/G]GCCCGCGTTTCTGTG	220441
rs11660288	snp	C/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808342	TTTGGACAATATTTT[C/T]TACACAGCCCAGCAG	220441
rs11663209	snp	C/T	0.0142736	0.0832652	intron-variant	RNF152	GRCh38.p7	18:61869624	AGAACTTAGCTGATC[C/T]AGGAGGGTGCCAGGA	220441
rs11664038	snp	G/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61820398	ATTTTATATCCAAGG[G/T]AATACATTTTTTTTT	220441
rs11664681	snp	A/G	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809756	AATATAAAAAACCTT[A/G]GATTAGAATAATAAA	220441
rs11875725	snp	A/C	0.302435	0.244439	intron-variant	RNF152	GRCh38.p7	18:61890395	CATAATTGCTAGAGC[A/C]AGACCCTGCAGCATT	220441
rs11876719	snp	A/G	0.33303	0.235809	intron-variant	RNF152	GRCh38.p7	18:61830587	TTCCTTCTTATGGCT[A/G]AGTAATATTCAATTG	220441
rs11876921	snp	C/T	0.47666	0.105476	intron-variant	RNF152	GRCh38.p7	18:61830562	ACCCACATTGTAACA[C/T]GTATCAGAATTCCTT	220441
rs11877369	snp	C/T	0.474363	0.110278	intron-variant	RNF152	GRCh38.p7	18:61876745	TAATAGAACCGTCTA[C/T]TCTACCCCGTAGGAT	220441
rs11877687	snp	A/C	0.325327	0.238382	intron-variant	RNF152	GRCh38.p7	18:61831123	TTTATAGAGATTAAA[A/C]CTTAACAGCACTCAA	220441
rs12327282	snp	A/G	0.109108	0.206518	intron-variant	RNF152	GRCh38.p7	18:61849634	GGTTTTAGATTATCC[A/G]AAACAAAATGGATCT	220441
rs12373176	snp	A/C	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833829	GGTGATACATCACCT[A/C]AGGTGACCTCTCTCA	220441
rs12373177	snp	A/T	0.341685	0.232581	intron-variant	RNF152	GRCh38.p7	18:61833904	AAAAAAGTTTCATCC[A/T]CAAGATAAAATATCA	220441
rs12373222	snp	C/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833569	AGACACACACAAACA[C/T]GATTTCCTGAGGAAG	220441
rs12386109	snp	A/T	0.162253	0.234095	intron-variant	RNF152	GRCh38.p7	18:61854917	ATAGCAGCAAGTTAC[A/T]TGATTTTCCTGAACT	220441
rs12456291	snp	G/T	0.325091	0.238456	intron-variant	RNF152	GRCh38.p7	18:61845930	TTGTGTGGGGGGGCG[G/T]GGTGATGAGGACTCA	220441
rs12457066	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61887119	GTTTTAAAGTCAGGC[A/G]GAGCAAAAGTCGAGG	220441
rs12604349	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61865712	TCAGAAAAGAATTTT[A/C/T]TGAACATTAGAGTTT	220441
rs12604567	snp	A/C	0.279195	0.248289	intron-variant	RNF152	GRCh38.p7	18:61844874	GCCTTTTAAAACAAA[A/C]AAAAAAAAGCATTTA	220441
rs12607054	snp	A/C	0.00943375	0.0680285	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808227	AGGACTGGCTAAGAC[A/C]CCATCTATAACAGAG	220441
rs12717144	snp	C/T	0.380724	0.213099	intron-variant	RNF152	GRCh38.p7	18:61863974	TCTCTTTCTGAAAAA[C/T]ACCCAGTCATTGGAC	220441
rs12953421	snp	C/T	0.274124	0.248833	intron-variant	RNF152	GRCh38.p7	18:61855332	AATTCATTATTTTGA[C/T]GATATCATAGTGATG	220441
rs12957662	snp	C/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61834729	TATTTGCAGGCAATT[C/G]AGAAATCATGAGTAT	220441
rs12961314	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61861213	ctcaccactcacatc[C/T]tgaatcactcagagc	220441
rs12963973	snp	C/G	0.297382	0.245469	intron-variant	RNF152	GRCh38.p7	18:61888239	ATGGACATCAAGAAC[C/G]ACCCAAAGGAGATGC	220441
rs12967834	snp	C/T	0.0310518	0.120672	intron-variant	RNF152	GRCh38.p7	18:61871551	GTTACTGCCCTCAGC[C/T]GACCAAATGAACAAA	220441
rs12970143	snp	C/T	0.299158	0.245119	intron-variant	RNF152	GRCh38.p7	18:61876197	ACGGGCATTGTCAAA[C/T]ACTACATTTTTTGTG	220441
rs12970913	snp	A/G	0.23031	0.249223	intron-variant	RNF152	GRCh38.p7	18:61837117	cttatgaagtatcac[A/G]cctaaatgttcgtct	220441
rs12971023	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810803	GTTTTGGTAAGAATT[A/C]CCTTGTAGGTGACAA	220441
rs12971027	snp	A/C	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810815	ATTACCTTGTAGGTG[A/C]CAATTTACTGAGAAT	220441
rs12971147	snp	A/C	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810848	TGGAAATGTCAAGGA[A/C]CAGCTTCTCTATCTA	220441
rs13381487	snp	A/G	0.210301	0.246828	downstream-variant-500B	RNF152	GRCh38.p7	18:61807644	ACCCTATTCATGAGA[A/G]CATTAATTGAAGGAC	220441
rs13381863	snp	C/T	0.473174	0.112665	intron-variant	RNF152	GRCh38.p7	18:61863930	AGCTCCCGCTCTAAT[C/T]GGCTGCCTTTTCCAT	220441
rs28395263	snp	G/T	0.0228947	0.104514	intron-variant	RNF152	GRCh38.p7	18:61834663	AGAAGGGGTGAAAAC[G/T]AACTGAAATTAGGCC	220441
rs28395312	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843179	TGAACAACTGTTGCT[A/G/T]AATGACTGAGAAAAC	220441
rs28398404	snp	A/G	0.02016	0.0983543	intron-variant	RNF152	GRCh38.p7	18:61840056	TCACTGCCATTGGGT[A/G]TCACTGCTCCCATGC	220441
rs28420234	snp	C/T	0.210301	0.246828	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810065	CCAATAAAATGTATA[C/T]AGTAGAACCTACCTC	220441
rs28436853	snp	A/C	0.0228947	0.104514	intron-variant	RNF152	GRCh38.p7	18:61834913	CTGAAAACCTGATAA[A/C]TCAGCGTCTGGGGGT	220441
rs28477857	snp	C/T	0.0225045	0.103662	intron-variant	RNF152	GRCh38.p7	18:61843143	AGGATTTTAGAATGC[C/T]AGGTAAGTGCCAAGA	220441
rs28478936	snp	A/T	0.0197687	0.0974348	intron-variant	RNF152	GRCh38.p7	18:61879982	AAAAAAAAAAAAAAA[A/T]TTTTTTTGTGCACAG	220441
rs28482142	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61818446	AAAAAAACAAAAAAC[A/C]AAAAACAAGAAAAAG	220441
rs28525583	snp	A/G	0.338523	0.233803	intron-variant	RNF152	GRCh38.p7	18:61833077	TTCCATTCCTCAGCT[A/G]TATCTACTAAAATTC	220441
rs28529692	snp	C/T	0.483995	0.0880135	intron-variant	RNF152	GRCh38.p7	18:61880935	TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG	220441
rs28563112	snp	C/T	0.350764	0.228794	intron-variant	RNF152	GRCh38.p7	18:61887688	GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA	220441
rs28571780	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859392	ACACTGTTCCCAGGG[A/C]TCCCAACACATGCGT	220441
rs28578687	snp	C/T	0.209997	0.246779	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810029	CCCACCTGCTTAAGT[C/T]CTTCAATGATTAATG	220441
rs28594579	snp	C/T	0.0551013	0.156571	intron-variant	RNF152	GRCh38.p7	18:61846949	TGCAAGTTAACCTTA[C/T]TGAGTATCTGCTTCT	220441
rs28617477	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61818438	AAATTAAAAAAAAAA[A/C]AAAAAACAAAAAACA	220441
rs28675903	snp	A/G	0.139225	0.224118	intron-variant	RNF152	GRCh38.p7	18:61840094	TGGGCACAGCTAGAA[A/G]ATAAATGTAACCTAA	220441
rs28684452	snp	C/T	0.0221141	0.102801	intron-variant	RNF152	GRCh38.p7	18:61848162	TTTCAAAAGCGCCTC[C/T]GGGCTCCTCTCACAT	220441
rs28701654	snp	A/G	0.33875	0.233717	intron-variant	RNF152	GRCh38.p7	18:61835489	TCAATTAAGGGAAAG[A/G]TTCATGAATAAGGAG	220441
rs28790659	snp	A/C	0.446641	0.154377	intron-variant	RNF152	GRCh38.p7	18:61861481	GTGTAAGTGTACTCA[A/C]TCCATAATGTTCACA	220441
rs33930800	in-del	-/T	0.336245	0.234652	intron-variant	RNF152	GRCh38.p7	18:61823463	ACCACACCCAGCTAA[-/T]TTTTTTTGTATTTTT	220441
rs33940699	in-del	-/A	0.33875	0.233717	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812857	AGTACATAAACCTAC[-/A]AAAAAAATTCTTTAA	220441
rs33984393	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61884244	AGCTGAAGAACAAAC[-/G]TCAGTCAGACCTTGT	220441
rs34025169	snp	C/T	0.294832	0.245947	intron-variant, splice-acceptor-variant	RNF152	GRCh38.p7	18:61868213	CTTACAGCATATATC[C/T]GTGTTATGTTTCAGG	220441
rs34073111	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61888551	CTTCTTGTTACATGA[-/T]TTTTGCCCCCATTGT	220441
rs34138491	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61874171	TACCCTGACATCTTA[-/G]GTAAAACCAAAGGCA	220441
rs34170984	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61887721	AAAAAAAAAAAAAAA[-/A]GAATGCTCCCTATTT	220441
rs34181406	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844066	AAGAAAGAGAGAAAG[A/C]CAGAAAGAAAGGAAA	220441
rs34207730	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61826340	TTCAGGGTAGTTTCA[-/T]GGCCACAAAGAAGAC	220441
rs34343311	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61830772	AGTGAAGGAGGAGTA[-/CA]GAAAAGATCCCTGAT	220441
rs34360893	snp	G/T	0.249603	0.25	intron-variant	RNF152	GRCh38.p7	18:61859391	CACACTGTTCCCAGG[G/T]CTCCCAACACATGCG	220441
rs34362018	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61887720	AAAAAAAAAAAAAAA[-/AA]GAATGCTCCCTATTT	220441
rs34388357	snp	A/C	0.423413	0.180077	intron-variant	RNF152	GRCh38.p7	18:61873313	ATTTAAAATTGTACT[A/C]AAAAATTCTGCAGTC	220441
rs34429051	snp	A/G	0.294576	0.245994	intron-variant	RNF152	GRCh38.p7	18:61867537	GGGGGAGCAGGGGCA[A/G]AGAGATATTTGAAAG	220441
rs34498934	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61820404	TATCCAAGGTAATAC[-/A]TTTTTTTTTCTTAAA	220441
rs34526463	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61887987	AGCAGCACATCTTCA[-/T]TTTGCTCAGCCCCTC	220441
rs34662029	in-del	-/G			utr-variant-5-prime	RNF152	GRCh38.p7	18:61816524	GCTGCTTCTCAGAGG[-/G]CCACCGCCCTGTGTC	220441
rs34663065	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61863454	AAAAAAAAAAAAAAA[-/A]GTAGCCCCTTGACTT	220441
rs34671190	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61862495	ACCCTCCATGAGGGG[-/G]ATCCCACCCTGTGCC	220441
rs34707375	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61886015	TTTTTTTTTTTTTTG[G/T]GGGCAAAGTAGGAGG	220441
rs34848581	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61836588	AATCTGACCATGTTC[-/C]AGCACCTTGATCTTA	220441
rs34901095	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61849971	CTGCCTATCTCTAAG[-/C]ATGTCTAAATATGGT	220441
rs34958570	snp	C/T	0.347253	0.230308	intron-variant	RNF152	GRCh38.p7	18:61872614	CTCTTTCCCTTCTGG[C/T]TTGCCCTACATTTGA	220441
rs34966668	in-del	-/A/AAAA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808412	AAAAAAAAAAAAAAA[-/A/AAAA]GCTCCTAAAATAAAT	220441
rs35036629	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61835748	TAGTGGGGTACATCC[-/C]TTTAATAATAATAAC	220441
rs35120921	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61845199	AAGCTATCCTCCCCC[-/C]ATCAGCCTCCCAAAG	220441
rs35125130	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61839071	AAAAAAAAAAAAAAA[-/A]GTACTAATAACTTTC	220441
rs35157847	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61816948	CTAGAGAAACTTTCC[-/C]TGCTTCCAATAAGTT	220441
rs35162554	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61824211	CAGGAGATAAGGATT[-/A]CTAGCTCTTATTCTG	220441
rs35190141	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61853315	TTTTTTTTTTTTTTT[-/T]GGAGACAGGTTACCC	220441
rs35234895	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61841064	GAAAGACCCATGGGG[-/G]CACATGGAGCAGCAG	220441
rs35303933	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61882289	TAGCACTGTGTGTGT[-/A]AAAATAAAGGCAATT	220441
rs35310776	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61885347	AGCCTCGGTCTTTTG[-/C]CCCAGGCTGGAGTGC	220441
rs35350173	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61848077	CAGAACATAAGCCCC[-/C]ACTGTGTGTTTCATT	220441
rs35403105	in-del	-/A/AA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811047	GCAAAAAAAAAAAAA[-/A/AA]TTAAATGATTTTTAA	220441
rs35442887	in-del	-/TA			intron-variant	RNF152	GRCh38.p7	18:61837673	CTAAGATACTTGATA[-/TA]GAAGAAAGCCTCAAA	220441
rs35444016	snp	A/G	0.28052	0.24813	intron-variant	RNF152	GRCh38.p7	18:61855041	TATTTTAAATAAGCT[A/G]ATGGTGGTGGGGAGA	220441
rs35494966	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61836897	ATAAATCATCAATAG[-/G]ATGCTAAAATCATTG	220441
rs35709206	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858893	GTTTGGTCAGCAAGC[C/T]TGAGACAAAACAAAA	220441
rs35725097	snp	A/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892695	TTCTCACAGATAGGA[A/G]CGATGTTGATGCAGA	220441
rs35743888	snp	C/T	0.00835141	0.0640778	intron-variant	RNF152	GRCh38.p7	18:61831823	GTAAAAACTTAAAGT[C/T]CTGTCATCAATAAGA	220441
rs35821984	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61825962	TTATCTATGTCAGGG[-/G]ACCCACAACCTTTTC	220441
rs35833108	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61869694	GAACTTCAAAGTAAA[-/A]TGAATGTCCAGTAAA	220441
rs35978592	in-del	-/GAAA	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61844138	AAGACAGAAAGAAAG[-/GAAA]GAAAGAAAGAAAGAA	220441
rs36037117	snp	A/G	0.296619	0.245615	intron-variant	RNF152	GRCh38.p7	18:61886789	AAACAGAAAGAAAAA[A/G]ACACTTCAATCGTAG	220441
rs36050564	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61830683	TAAAGGAAAGAGGGG[-/G]CAAGGCTGGAATGAA	220441
rs55637496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873823	CAAGGAAAGTGGACT[C/T]GTTTTCCGAGAAAAT	220441
rs55794477	in-del	-/GTGT	0.0452528	0.143452	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810272	TGTGTGTGTGTGTGT[-/GTGT]AGTAAGTCAGTTGTG	220441
rs55829309	snp	A/G	0.456214	0.141336	intron-variant	RNF152	GRCh38.p7	18:61830171	GGACTACAGGCACAC[A/G]CCACTGTAGTCTGGC	220441
rs55853108	snp	A/G	0.336474	0.234568	intron-variant	RNF152	GRCh38.p7	18:61863254	CCTGGCTAACACAGT[A/G]AAATCCCATCTCTAC	220441
rs55856123	snp	A/T	0.31721	0.240796	intron-variant	RNF152	GRCh38.p7	18:61833107	CACTGACTTCTACCA[A/T]CAGGAAATTACTATT	220441
rs55923228	snp	A/G	0.33303	0.235809	intron-variant	RNF152	GRCh38.p7	18:61830278	TGATCCACCCACCTC[A/G]TCCTCCCAAAGTGCT	220441
rs56019954	snp	C/G	0.331411	0.236373	intron-variant	RNF152	GRCh38.p7	18:61830170	GGGACTACAGGCACA[C/G]ACCACTGTAGTCTGG	220441
rs56039619	snp	A/G	0.154329	0.23097	intron-variant	RNF152	GRCh38.p7	18:61855406	TGTAGTGGGGGAGGC[A/G]CAGCCAGGACTGTGC	220441
rs56043347	snp	G/T	0.330016	0.236849	intron-variant	RNF152	GRCh38.p7	18:61828932	CAGGTTGAACTGGAA[G/T]AAGGAGCACCTATGT	220441
rs56110002	in-del	-/A	0.387642	0.208697	intron-variant	RNF152	GRCh38.p7	18:61828629	TGGTTTAGAAAAAAA[-/A]TGTGATAATATTCTC	220441
rs56116436	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815304	TAAAATGACTGTCCA[C/T]TTTGACTTATTTTGT	220441
rs56122932	snp	C/T	0.328148	0.237472	intron-variant	RNF152	GRCh38.p7	18:61821648	GCAAGGGTCTCCAAC[C/T]CCCAGGCCACCAACC	220441
rs56196720	snp	G/T	0.385932	0.209815	intron-variant	RNF152	GRCh38.p7	18:61829512	AGAGAGAGATATATA[G/T]ATATCAGGGGAGGGA	220441
rs56255109	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809694	AGGTCCCTCAGTACT[C/T]TGCCCCAAATATTAC	220441
rs56288246	snp	C/T	0.377977	0.21476	intron-variant	RNF152	GRCh38.p7	18:61851718	TAATATTTCCATTTA[C/T]AGTTGAGAAAATTAA	220441
rs56317690	snp	A/G	0.45574	0.142025	intron-variant	RNF152	GRCh38.p7	18:61830322	TGAGCCACAGTGCCC[A/G]GCCCTTTCCAGAGCT	220441
rs56349051	in-del	-/T	0.404907	0.196224	intron-variant	RNF152	GRCh38.p7	18:61826563	TATGCATATATAAAC[-/T]TTTTTTTCCTCTTTA	220441
rs56384369	snp	A/G	0.326976	0.237854	intron-variant	RNF152	GRCh38.p7	18:61831322	CTCGGGGAAATGCTC[A/G]GATTCATCATCTTTC	220441
rs56397865	in-del	-/AA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809877	AAAAAAAAAAAAAAA[-/AA]GTCATTGGCTCGACT	220441
rs56412400	snp	G/T	0.386504	0.209444	intron-variant	RNF152	GRCh38.p7	18:61829506	GAGGGGAGAGAGAGA[G/T]ATATATATATCAGGG	220441
rs56881598	snp	C/G	0.137187	0.223099	intron-variant	RNF152	GRCh38.p7	18:61860745	GGTATCCAGAAGAAG[C/G]CACTGCTGTCACAGG	220441
rs57028779	snp	A/G	0.203575	0.245652	intron-variant	RNF152	GRCh38.p7	18:61820052	AAAAAGAATCCGGCC[A/G]GGCATGGTGGCTCAC	220441
rs57103248	snp	C/G	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61825194	TGCCATGGTAAACAA[C/G]AGTCCTACCCTCAAG	220441
rs57295716	in-del	-/A	0.0399052	0.1355	intron-variant	RNF152	GRCh38.p7	18:61862553	AGCTTCGGTAAAAAA[-/A]CCCAAGCGGACAGGG	220441
rs57520734	snp	A/T	0.336702	0.234484	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808595	CTACATGGCTTATGT[A/T]GGGAGTTTGTAACAG	220441
rs57741938	snp	A/T	0.0573587	0.15934	intron-variant	RNF152	GRCh38.p7	18:61832660	CCCAAATTCTACCTG[A/T]GAACTAAAAAAACAG	220441
rs58003808	snp	C/G	0.0283406	0.115616	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814007	CTTACACAATAAAAT[C/G]GCATTTTAACCTAAT	220441
rs58153277	snp	C/T	0.15665	0.231917	intron-variant	RNF152	GRCh38.p7	18:61857079	AATATAATTAAAATA[C/T]AGGCAGGGGAACAGG	220441
rs58154775	snp	C/T	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61821430	GTAATGATGATGATT[C/T]GTTAGGTAAAGAGAA	220441
rs58312360	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858442	ATCTCCCCTGCAACC[A/G]TATACCCTAGGATGA	220441
rs58383851	snp	A/G	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61874477	TTCAAAATAATGTGC[A/G]ACTATTTTAAAAAGC	220441
rs58415649	snp	A/G	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61873614	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	220441
rs58596322	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859885	ACCTCAAAGAAAAAA[A/G]AAAAGAAAAGAAAAG	220441
rs58772361	in-del	-/CACA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813313	ACACACACACACACA[-/CACA]TACACAAGAATGCAC	220441
rs58844907	snp	A/C	0.253824	0.249971	intron-variant	RNF152	GRCh38.p7	18:61891835	CTGTCACAGATACCA[A/C]GGTGTTACTGCAATG	220441
rs59051201	snp	A/G	0.0603597	0.1629	intron-variant	RNF152	GRCh38.p7	18:61870091	TATTCCAAACCTCAC[A/G]CTCTCTTGGAAAGAA	220441
rs59373633	in-del	-/A	0.484138	0.0876334	intron-variant	RNF152	GRCh38.p7	18:61887409	TCTGTCAAGGAGCAG[-/A]AACAGCAATAGTAAG	220441
rs59438030	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812138	AAGCGCTATCACCCA[A/G]AACTGCATCGTTCAA	220441
rs59499904	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61849859	GGTTTGAGCCACCAT[A/G]CCCTGACATCATCAA	220441
rs59667570	in-del	-/A	0.261332	0.249743	intron-variant	RNF152	GRCh38.p7	18:61868715	AAAAATAAAAAAAAA[-/A]TAAGTACAGGTTTTA	220441
rs59692853	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61874425	TCTTGATGAAAGAGC[C/T]CTCAATCAACCAACC	220441
rs59712370	snp	A/G	0.161596	0.233848	intron-variant	RNF152	GRCh38.p7	18:61829637	AGGGCGGTTGAAGGG[A/G]AGTGAAGAGGGGAGG	220441
rs59783828	snp	A/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61874523	TCCTTAAGGAGGCAG[A/T]ACTAGTAAGAGACAT	220441
rs59898273	snp	A/G	0.0197687	0.0974348	intron-variant	RNF152	GRCh38.p7	18:61856602	GTTGATAACTGGAGT[A/G]TTTAGATTTGATACC	220441
rs60209985	snp	C/G/T	0.0607709	0.163542	intron-variant	RNF152	GRCh38.p7	18:61874476	ATTCAAAATAATGTG[C/G/T]AACTATTTTAAAAAG	220441
rs60266996	snp	A/G	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61819067	GGAAAGAAGGTAAGC[A/G]ATTACAGAATTATTT	220441
rs60310473	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844091	AGGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG	220441
rs60358145	snp	G/T			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814919	GAGACCACTCGCTGG[G/T]TCAAGATGTCCAAGA	220441
rs60538913	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61846027	CCATGTGAGGACACA[A/G]CAGATGCCCTTTATG	220441
rs60594023	in-del	-/TTTGTTTG	0.48797	0.0888421	intron-variant	RNF152	GRCh38.p7	18:61885310	TTGTTTGTTTGTTTG[-/TTTGTTTG]AGACAGAGCCTCGGT	220441
rs60822775	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886078	CAACTAATTTTGTTA[A/G]AATCATGACCCTCAT	220441
rs60839455	in-del	-/G	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61884243	CAGCTGAAGAACAAA[-/G]CTCAGTCAGACCTTG	220441
rs60860954	snp	C/G	0.0298908	0.118541	intron-variant	RNF152	GRCh38.p7	18:61861541	AAAATATATCCCTGT[C/G]ATCAAGTGAGGCATG	220441
rs60918332	snp	A/C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814921	GACCACTCGCTGGGT[A/C/T]AAGATGTCCAAGAAG	220441
rs61119907	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61857758	CATTCTAGTTTTGGA[A/T]AATAGCCTATCACAA	220441
rs61200710	in-del	-/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813309	ACACACACACACACA[-/C]ACACACATACACAAG	220441
rs61280931	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874971	TGAACAAGCCCAGCC[A/C/T]TCAAAGACCCACCTG	220441
rs61472157	snp	C/T	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61874594	CTGAAGGTGGCAGTA[C/T]ATAGGCTGAGTGGCA	220441
rs61545985	snp	A/G	0.0158469	0.0875917	intron-variant	RNF152	GRCh38.p7	18:61887040	ACAGAATGTGCTAGA[A/G]TAAGAAAGAGGCAAT	220441
rs61577550	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895800	CCACCGCGCCTTTTT[G/T]TTTTTTTTTTTTTTT	220441
rs61693209	snp	A/G	0.135484	0.22223	intron-variant	RNF152	GRCh38.p7	18:61860523	GTTGATAGTGAGGCT[A/G]GTGTAAAGAAACCTA	220441
rs62094960	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61891434	TGTTTATTCTTTCTA[A/T]TAAAAAAAAAACCAC	220441
rs62094961	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61891436	TTTATTCTTTCTATT[A/T]AAAAAAAAACCACAC	220441
rs62094962	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893440	GGCGATTTCTCTACT[C/T]TCTCCAGACCCAGGC	220441
rs62096264	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813309	ACACACACACACACA[A/C]ACACACATACACAAG	220441
rs62096265	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61820172	GTCTCTACTAAAAAT[A/G]CAAAAAATTAGCCAG	220441
rs62096266	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61820417	ACATTTTTTTTTCTT[A/T]AAACAAAACAAAATA	220441
rs62096273	snp	C/T	0.333261	0.235728	intron-variant	RNF152	GRCh38.p7	18:61830771	GAGAGTGAAGGAGTA[C/T]AGAAAAGATCCCTGA	220441
rs62096301	snp	G/T	0.316485	0.240998	intron-variant	RNF152	GRCh38.p7	18:61835198	AATACAGCTCCACAG[G/T]ACAAAATAGCATATT	220441
rs62096302	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844059	AAGAAAAAAGAAAGA[A/G]AGAAAGACAGAAAGA	220441
rs62096303	snp	A/G	0.40595	0.195396	intron-variant	RNF152	GRCh38.p7	18:61844426	CTATTGGAAAATCAT[A/G]AAAACAATACCTTAC	220441
rs62096305	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61855422	CAGCCAGGACTGTGC[A/G]TTCCATAGCCCTTAC	220441
rs67262212	in-del	-/TTT	0	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896218	TTTTTTTTTTTTTTT[-/TTT]GAGACAGGGTCTCAC	220441
rs71179000	in-del	-/T	0.277778	0.248452	intron-variant	RNF152	GRCh38.p7	18:61880914	CTCTCTCTAGTTTTC[-/T]TTTTTTTTTTTTTTT	220441
rs71352546	snp	A/C	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61819894	GGTGTGGTGGTGGAC[A/C]CCTGTAATCCCAGCT	220441
rs71352547	snp	A/C	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61819978	GTGAGGCAACATCGC[A/C]CCACTGCACTCCACC	220441
rs71352548	snp	A/C	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61822189	AGTGAAAAACAGACC[A/C]CAAAGAGAAGAACAG	220441
rs71352549	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61823858	CCTGGCTGCAGCCTA[A/G]GTGCTGTCCCTGTCT	220441
rs71352550	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61854397	AATAATCTGAATTTG[C/T]TAAGACATACACACA	220441
rs71352551	snp	A/C	0.298651	0.24522	intron-variant	RNF152	GRCh38.p7	18:61878068	AGATTAGAAAGAGAA[A/C]GAGGGTAGAAAAGGC	220441
rs71352552	snp	G/T	0.181022	0.240296	intron-variant	RNF152	GRCh38.p7	18:61879020	AAAGGAAAGTAAGTC[G/T]GCCTGAGGGAGCTGG	220441
rs72536297	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61884242	GCAGCTGAAGAACAA[-/G]ACTCAGTCAGACCTT	220441
rs72998417	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809640	CAGGGAAGCACTCCC[A/G]CAAAAACAAAGAAAA	220441
rs72998418	snp	C/T	0.0225045	0.103662	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810809	GTAAGAATTACCTTG[C/T]AGGTGACAATTTACT	220441
rs72998423	snp	C/T	0.0215162	0.101465	missense	RNF152	GRCh38.p7	18:61816048	CCTTGCAGAGGCTGC[C/T]GTTCAGCAGGGATGG	220441
rs73002584	snp	A/G	0.444444	0.157135	intron-variant	RNF152	GRCh38.p7	18:61844170	AAGGAAGGGAGGAAG[A/G]GAGGAAGAGAGGAAG	220441
rs73002587	snp	G/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61844654	AACAGGCCAACAAAT[G/T]ATTCATCTTGTGTCT	220441
rs73002590	snp	C/T	0.0221141	0.102801	intron-variant	RNF152	GRCh38.p7	18:61846761	GAATTATTAATACTG[C/T]TCTCCTCACCTTCAT	220441
rs73002600	snp	C/T	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61864123	CTCTCCAACAACAAT[C/T]GGGTGTCCCAGAATT	220441
rs73004405	snp	A/C	0.231189	0.249291	intron-variant	RNF152	GRCh38.p7	18:61870455	AAGAAAGAGGAGACC[A/C]CGCCTGTCACCTTAC	220441
rs73004415	snp	A/C	0.0376037	0.131863	intron-variant	RNF152	GRCh38.p7	18:61877968	AAGGGAGCATCTGCT[A/C]CACAAGGTCTCTTAG	220441
rs73004444	snp	C/G	0.231775	0.249335	intron-variant	RNF152	GRCh38.p7	18:61891863	ATGTAAAAGAGAGTA[C/G]ACCAGGAGCCTTTGG	220441
rs73004445	snp	C/T	0.0123036	0.0774623	splice-donor-variant, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892794	GATCGTGGGGGGTTA[C/T]CTGTATCTGTCACCG	220441
rs73456334	snp	A/G	0.00795532	0.062565	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814895	GCGAGTGTTGCAGGT[A/G]ACGTGTAGGAGACCA	220441
rs73456336	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61820666	ACAGGAAAACCCTCA[A/G]TTGCAAATGAGGCTG	220441
rs73458427	snp	A/G	0.107341	0.205301	intron-variant	RNF152	GRCh38.p7	18:61839385	AGATTTCCAGAAGTT[A/G]TTAATATTTCATAGA	220441
rs73458428	snp	C/T	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61840479	CTGTCTCTAAGTGGT[C/T]CTTCTTCTCTTCACA	220441
rs73458436	snp	C/G	0.105569	0.204058	intron-variant	RNF152	GRCh38.p7	18:61845904	ATGTGAAGGTATTAA[C/G]AGGTGGGGCTTTGTG	220441
rs73458437	snp	A/C	0.0850919	0.187897	intron-variant	RNF152	GRCh38.p7	18:61846272	TTAATAAAAAACAAT[A/C]CCAAAAAACTGTCTT	220441
rs73458440	snp	A/G	0.0825414	0.185628	intron-variant	RNF152	GRCh38.p7	18:61849101	AGTCTGTGTCAACCC[A/G]TACTATGACTCCCTG	220441
rs73458444	snp	A/G	0.0456336	0.143994	intron-variant	RNF152	GRCh38.p7	18:61850928	CAGCTCTGGGCACAC[A/G]GAAATGCCCAGTCAT	220441
rs73458450	snp	G/T	0.030665	0.119967	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852066	CAGAGCCAGCCAGGG[G/T]GCACATGTGCTCTCA	220441
rs73458454	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61858036	AGCAGAGCCACCCCA[C/G]CAGGGGCTGAAAAAG	220441
rs73458457	snp	A/G	0.00597247	0.0543191	intron-variant	RNF152	GRCh38.p7	18:61859018	ATTACAGGAGGGTGA[A/G]GGAGGCCCTTTCTAA	220441
rs73458465	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61866653	TTCCCTGTGCTTCTC[C/T]TCCATGTCTCCTCTC	220441
rs73458467	snp	C/T	0.0158469	0.0875917	intron-variant	RNF152	GRCh38.p7	18:61869058	TTATCAGAAGAGATT[C/T]TGAGAATATTCTAAC	220441
rs73458469	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61871301	TTTCATTCCTCTGGG[C/T]CTGCCTCTGGATTCC	220441
rs73458472	snp	A/C	0.0158469	0.0875917	intron-variant	RNF152	GRCh38.p7	18:61878312	CATCCCACACTGCAC[A/C]GGACGGTCTTCCCAC	220441
rs73458476	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61881222	CGGCCTTCTCTCTCT[C/T]GTTTTCTTATTTTCA	220441
rs73963595	snp	C/T	0.0279526	0.114869	intron-variant	RNF152	GRCh38.p7	18:61844994	AGGGCCATAAGTGGA[C/T]ACGAGTGCTGAAAAC	220441
rs73963599	snp	A/C	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61876873	TGCTTTATATGGGGG[A/C]ACAAAACACTAGACT	220441
rs73963602	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895850	GGAAGCCCTGTGAGC[C/T]AGTGGGGACTCTAGG	220441
rs74317463	snp	C/G	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61829254	AGGGCACAGCCTGGA[C/G]GACTGGCCTGCCCAG	220441
rs74346608	snp	A/C	0.0807149	0.183963	intron-variant	RNF152	GRCh38.p7	18:61861940	CAACATTGGGCATTA[A/C]ATTTCAACATGAGAT	220441
rs74393722	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61883384	TAAACAGTTCTCTTC[C/T]TTTTAATAATAATAA	220441
rs74408225	snp	C/T	0.234109	0.249494	intron-variant	RNF152	GRCh38.p7	18:61830909	TGAATCTTGAGATTT[C/T]GTACCTAGCAAAGTC	220441
rs74468340	snp	C/T	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61862348	GAAACTAAGGCTCAG[C/T]TGGATCAGGGACTGC	220441
rs74487003	snp	A/G	0.0368353	0.130617	intron-variant	RNF152	GRCh38.p7	18:61829072	GCCCAGGGTGGTTAC[A/G]GGTAGGGACCAGAGC	220441
rs74550037	snp	C/G	0.040671	0.13668	intron-variant	RNF152	GRCh38.p7	18:61878818	CCTTCATGGCCTAAT[C/G]AACTCCTAAAGGCCC	220441
rs74572179	snp	C/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61852521	CCTCAACAGACCACC[C/T]ACTTCTCTCAAAACT	220441
rs74577203	snp	A/G	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61872541	CCAAATATTCATGAA[A/G]TCATGCCCCTCTCCC	220441
rs74579247	snp	A/C	0.0209421	0.100162	intron-variant	RNF152	GRCh38.p7	18:61875495	CCTTTACATGGTCAG[A/C]TCTCTAGAGAGCTTC	220441
rs74626521	snp	C/T	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61869284	AAAAGCTGTCAGGGG[C/T]CTTCTTCCAATCATA	220441
rs74639088	snp	C/T	0.040671	0.13668	intron-variant	RNF152	GRCh38.p7	18:61884229	TTCTCCCCCATTTTG[C/T]AGCTGAAGAACAAAC	220441
rs74779528	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809131	CTATACTCTTCCTTT[A/G]TTAAGTATTTTCTCC	220441
rs74788822	snp	G/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61873046	TATGAATGCTTCTAC[G/T]TACCAGATTTGGGGT	220441
rs74813643	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864164	TTGACCCTAACTACC[C/T]GGAGTCACAGACCCC	220441
rs74843889	snp	C/G	0.0217236	0.101931	intron-variant	RNF152	GRCh38.p7	18:61847600	TCTTAAAACACACCT[C/G]AGAGAAAGCAAGACA	220441
rs74845201	snp	C/T	0.0142736	0.0832652	intron-variant	RNF152	GRCh38.p7	18:61857427	AACTGCTTTAGAACC[C/T]TTAGGGCCTCAGAAT	220441
rs74853036	snp	G/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875409	CAAATTTAATTGTCA[G/T]TGCATGCAAGTGTCC	220441
rs74944401	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61816612	TTCTGAGAGAGACAA[A/G]TAATGCAAACAATCT	220441
rs75000643	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895516	CTGTTTTTTTTTTTT[G/T]GAAGATGGACTCTCG	220441
rs75023786	snp	A/C	0.0314385	0.121371	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893449	TCTACTCTCTCCAGA[A/C]CCAGGCAGCGCTCCC	220441
rs75074470	snp	C/T	0.0275645	0.114116	intron-variant	RNF152	GRCh38.p7	18:61850764	ATGGTTTATCCAAAC[C/T]GCTTGTTTGAGCTCA	220441
rs75080661	snp	C/T	0.0486741	0.148216	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893602	CTGCACAAAAGACCC[C/T]CAACATCTGGCCCTT	220441
rs75096945	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61834684	AAATTAGGCCATTTT[A/T]AAAAAAAATTAAGCA	220441
rs75123832	snp	G/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61834418	TTTCTAGAATGATCA[G/T]ATTTTGTGTCCTTTT	220441
rs75151951	snp	A/G	0.0170251	0.090679	intron-variant	RNF152	GRCh38.p7	18:61823841	ACTGTGGGCCCAATT[A/G]GCCTGGCTGCAGCCT	220441
rs75204733	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61879473	TAGATACTGAGTGAC[A/G]ACTGTATATATGGTA	220441
rs75236654	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61854678	TCTACTATGATGGTC[A/C]TACTGCTATTGGTAA	220441
rs75241914	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61854116	TCCCCGTGACAAGGT[C/G]ATGTTTGCAATATTT	220441
rs75379469	snp	C/T	0.02016	0.0983543	intron-variant	RNF152	GRCh38.p7	18:61848105	ATTTGGGGCTGCATT[C/T]CCAGCATCTAGAACT	220441
rs75395839	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61870835	CCTAACTCCTTCTCA[A/G]CCTCTGATGCCCACC	220441
rs75410480	snp	C/G	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61827360	ATGTATGATTTCAGA[C/G]GAGTAGAACTTCATT	220441
rs75414484	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61838802	AAAGTCTTCACCCAG[C/T]CTTTTCTCATGACTT	220441
rs75439340	snp	C/T	0.0165278	0.0893908	intron-variant	RNF152	GRCh38.p7	18:61860734	GTGGTTCAGGAGGTA[C/T]CCAGAAGAAGGCACT	220441
rs75453798	snp	A/G	0.159622	0.233092	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852101	ACCCAGGAATATGAC[A/G]AGGCCAGCAGCAATG	220441
rs75478650	snp	A/G	0.210301	0.246828	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808563	AGCCGTAGGGTGGGA[A/G]GAACCCTGGATTGCA	220441
rs75481334	snp	A/G	0.0425829	0.139564	intron-variant	RNF152	GRCh38.p7	18:61819554	AGCAGGATCTTGCAG[A/G]GTATTGCAATGAGGT	220441
rs75529025	snp	C/G	0.0955749	0.196603	intron-variant	RNF152	GRCh38.p7	18:61848604	TCGGAAGGAACTGTA[C/G]GTAGGTCTATGCAGG	220441
rs75533121	snp	C/T	0.113334	0.209338	intron-variant	RNF152	GRCh38.p7	18:61867903	TAAAAATACACAAAA[C/T]GCACATAAAAATACA	220441
rs75550415	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61821431	TAATGATGATGATTC[G/T]TTAGGTAAAGAGAAG	220441
rs75578024	snp	C/T	0.132066	0.220435	intron-variant	RNF152	GRCh38.p7	18:61826579	TTTTTTTCCTCTTTA[C/T]ATGTTTTTGGTTACT	220441
rs75590864	snp	C/T	0.0777841	0.181223	intron-variant	RNF152	GRCh38.p7	18:61866554	GGGCCTACGCATCCT[C/T]TGGTGACTTGGCTAC	220441
rs75619180	snp	A/T	0.0236746	0.106192	intron-variant	RNF152	GRCh38.p7	18:61846794	GTAACAAAGCCAGAC[A/T]ATGCAATGCACTGAT	220441
rs75655734	snp	G/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61884504	ACCTACAGGAAGCTA[G/T]AAGGCAGGGATTTTT	220441
rs75659514	snp	C/T	0.338523	0.233803	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814219	CTTGAAGATAACAGA[C/T]AGCATGTAAATAAAT	220441
rs75685189	snp	A/C	0.0872718	0.189788	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893683	GAGAAGGCGCGAGAC[A/C]AGGGGACCGGGAGAA	220441
rs75701422	snp	C/T	0.204189	0.245767	intron-variant	RNF152	GRCh38.p7	18:61825740	AAAGGTCTCTCTCTG[C/T]TATAGCCCTCCAGTG	220441
rs75725321	snp	A/G	0.0166325	0.0896639	intron-variant	RNF152	GRCh38.p7	18:61834253	GGTCTGGAACCAAAA[A/G]AGAGAAGGACAGCAT	220441
rs75733844	snp	C/T	0.0685596	0.171987	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813396	ATTTAAACAATGTTT[C/T]TTAGGTCAGTAAGAC	220441
rs75738910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890611	CCTATCTTGCTGGTA[C/T]GTCACTGTTTAAAAA	220441
rs75744069	snp	A/G	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61858986	GTTTCTTACGCGCCG[A/G]GTGATGTCAATATCC	220441
rs75857642	snp	C/T	0.137527	0.223271	intron-variant	RNF152	GRCh38.p7	18:61836428	GGAGGTAATTAGGTT[C/T]AGATGAGGTCATGAG	220441
rs75860267	snp	A/T	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811060	GGCAAAAAAAAAAAA[A/T]TTAAATGATTTTTAA	220441
rs75950697	snp	A/G	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61888340	AAAATCCCTAAGCAT[A/G]TAACAAGCACAGACG	220441
rs75956513	snp	A/C	0.0930568	0.194599	intron-variant	RNF152	GRCh38.p7	18:61857217	ACAGGGAGAAAGTGC[A/C]GACACTTTTCTATTT	220441
rs76000113	in-del	-/GAG			intron-variant	RNF152	GRCh38.p7	18:61830768	CTGAGAGTGAAGGAG[-/GAG]TATAGAAAAGATCCC	220441
rs76024585	snp	C/T	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61824536	TTAGAAATTTCTCCC[C/T]TGATGCCTTCAGCTT	220441
rs76065278	snp	A/C	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61871092	TTAGGCTTCGATTCA[A/C]ACCATTGGCTACTAC	220441
rs76105401	snp	C/T	0.0437281	0.141251	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812768	TGGTTTGATAGTTGT[C/T]TTTCAACATCTATAC	220441
rs76151298	snp	C/G	0.0733688	0.176922	intron-variant	RNF152	GRCh38.p7	18:61841733	AGCCTCTCCATGAAA[C/G]CGCAAGTGAAGAACT	220441
rs76186745	snp	C/T	0.117886	0.21224	intron-variant	RNF152	GRCh38.p7	18:61872542	CAAATATTCATGAAA[C/T]CATGCCCCTCTCCCA	220441
rs76202047	snp	C/T	0.0566069	0.158427	downstream-variant-500B	RNF152	GRCh38.p7	18:61808027	ATTTTTTTTCTTTTC[C/T]TGGGGTTAGGAGGGG	220441
rs76322021	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844870	AATGGCCTTTTAAAA[A/C]AAAAAAAAAAAAGCA	220441
rs76324537	snp	C/G	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61868985	CCAGTTTCATGATGA[C/G]AGTAACTAAAAAGCA	220441
rs76375000	snp	A/C	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810239	TAATAACAGTTTTTT[A/C]CTGAATTTTAACTCC	220441
rs76383668	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884243	GCAGCTGAAGAACAA[A/G]CTCAGTCAGACCTTG	220441
rs76405629	snp	A/G	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61833566	CACAGACACACACAA[A/G]CATGATTTCCTGAGG	220441
rs76417275	snp	C/T	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61869036	AGGTTTTTATAAGCA[C/T]TTGAGGTTATCAGAA	220441
rs76427746	snp	C/T	0.162253	0.234095	intron-variant	RNF152	GRCh38.p7	18:61829764	AGGAGTAGCTGGAAG[C/T]GGAAGTTCTTATGTT	220441
rs76468101	snp	A/C	0.0437281	0.141251	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813343	GCACACCCCAACAAA[A/C]AGGTACACAAATAAC	220441
rs76472121	snp	A/G	0.0142736	0.0832652	intron-variant	RNF152	GRCh38.p7	18:61843434	TCACCCTATCATCCA[A/G]CAATTCCACCTCTGA	220441
rs76495131	snp	A/G	0.0803491	0.183626	intron-variant	RNF152	GRCh38.p7	18:61831182	TAAGTACTTAGAAGC[A/G]GTTCTGTGCACCAGG	220441
rs76513840	in-del	-/A	0.216048	0.247684	intron-variant	RNF152	GRCh38.p7	18:61866901	AAAGCAAAACAACAC[-/A]AAAAAAAACAGACTT	220441
rs76554779	snp	A/T	0.0337553	0.125452	intron-variant	RNF152	GRCh38.p7	18:61889879	GAGGAAGAGAAAGTC[A/T]GTAAGTAACACCTCT	220441
rs76556991	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61873043	ACATATGAATGCTTC[C/T]ACGTACCAGATTTGG	220441
rs76563981	snp	C/T	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61869472	GAATGCCCTGTCACC[C/T]CACCACAGACGGCAC	220441
rs76580871	snp	A/G	0.172028	0.23753	downstream-variant-500B	RNF152	GRCh38.p7	18:61807588	TATGATCCAGTTATC[A/G]AAAGACAGGATGCTT	220441
rs76582633	snp	C/T	0.0437281	0.141251	intron-variant	RNF152	GRCh38.p7	18:61817190	AGGCATCTTTCATCT[C/T]TCCCAACAAATCATT	220441
rs76607281	snp	C/T	0.203267	0.245593	intron-variant	RNF152	GRCh38.p7	18:61820917	CTCTGAGCCTGCTTT[C/T]TCCCTGGCCAAGCAG	220441
rs76623361	snp	A/G	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61871907	TGTGAGGGAGCCTCC[A/G]AGAAAGGATCCTATA	220441
rs76626540	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875283	CTATATGGAACAGTC[C/T]TTAAGCACCGTCTGT	220441
rs76764741	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895517	TGTTTTTTTTTTTTT[G/T]AAGATGGACTCTCGC	220441
rs76809447	snp	C/T	0.0205511	0.0992634	intron-variant	RNF152	GRCh38.p7	18:61854102	CACTGCTTATTGACT[C/T]CCCGTGACAAGGTGA	220441
rs76858232	snp	C/T	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61882650	TAAGGGCCTTATCAG[C/T]CTCCATCAATCCCAC	220441
rs76862350	snp	A/T	0.0998734	0.199905	intron-variant	RNF152	GRCh38.p7	18:61829629	GACATCCTAGGGCGG[A/T]TGAAGGGGAGTGAAG	220441
rs76930899	snp	C/T	0.0569829	0.158885	intron-variant	RNF152	GRCh38.p7	18:61818054	CTTTTTCCTTTCCAA[C/T]TTCCTTTGTGAAATT	220441
rs76950134	snp	A/G	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61874347	ACATATTGTATTTCC[A/G]ATTACAGATACAGGA	220441
rs76967642	snp	A/C	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61875572	CTGGGCGTGGATTAC[A/C]CACGAAGGTCAGCTC	220441
rs77008788	snp	A/G	0.0733688	0.176922	intron-variant	RNF152	GRCh38.p7	18:61841064	AGAAAGACCCATGGG[A/G]CACATGGAGCAGCAG	220441
rs77013698	snp	A/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810238	CTAATAACAGTTTTT[A/T]ACTGAATTTTAACTC	220441
rs77030205	snp	A/G	0.0596104	0.162024	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868183	TAGAGGTTGGCCTTC[A/G]GGTGTTGCTGTAGAC	220441
rs77089753	snp	G/T	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61832522	ATTAAGCCTGTTTAA[G/T]CCACAAATAACTGCT	220441
rs77090387	snp	C/T	0.118584	0.212673	downstream-variant-500B	RNF152	GRCh38.p7	18:61807716	CTACTTCACAGGGGC[C/T]GCATGAAGTTGTTCT	220441
rs77094388	snp	A/T	0.0599851	0.162463	intron-variant	RNF152	GRCh38.p7	18:61871861	AAGCCTCTGATAGGT[A/T]CATATCTTCATGGCA	220441
rs77183416	snp	C/T	0.0360663	0.129354	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811220	CCAATTTTGAAACAA[C/T]ATAAGTTTTCAAATA	220441
rs77207352	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811738	AGGGATTTCATTAGG[C/T]TTTTTTTTTCCTGTA	220441
rs77222024	snp	A/C	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61847613	CTCAGAGAAAGCAAG[A/C]CACCAATGGTGATAC	220441
rs77227947	snp	A/G	0.108755	0.206276	intron-variant	RNF152	GRCh38.p7	18:61818966	AAGGAATCAGGGGGA[A/G]TTTAGTGAAAAATCT	220441
rs77256844	snp	C/T	0.0599851	0.162463	intron-variant	RNF152	GRCh38.p7	18:61872689	CTCATTATTCTCTTC[C/T]TCCACAACTATGTCA	220441
rs77258967	snp	C/T	0.1652	0.235179	intron-variant	RNF152	GRCh38.p7	18:61837116	CCTTATGAAGTATCA[C/T]GCCTAAATGTTCGTC	220441
rs77283504	snp	C/G	0.0379877	0.132479	intron-variant	RNF152	GRCh38.p7	18:61832539	CACAAATAACTGCTT[C/G]AGTTTCAGTTTTCAT	220441
rs77304451	snp	A/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61879981	AAAAAAAAAAAAAAA[A/T]TTTTTTTTGTGCACA	220441
rs77313467	snp	A/C	0.0803491	0.183626	intron-variant	RNF152	GRCh38.p7	18:61833228	TTCTCACAAACCATT[A/C]GCTGATGTAGGTCGC	220441
rs77323740	snp	C/T	0.0633504	0.166319	intron-variant	RNF152	GRCh38.p7	18:61821348	AGCCTCTCTGATTTA[C/T]GCACTGATTTGTTCT	220441
rs77407256	snp	A/G	0.148326	0.228391	intron-variant	RNF152	GRCh38.p7	18:61834779	CAGTATGCTTTTATG[A/G]TATCTCCTCGCAGAA	220441
rs77410061	snp	A/C	0.00914312	0.0669923	intron-variant	RNF152	GRCh38.p7	18:61822900	GCCATCTACTTAAAT[A/C]TTCAACAAAATATAA	220441
rs77535457	snp	C/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61891955	TCCCTGCTACTAGTG[C/T]AGGATGCGCAGGACT	220441
rs77601539	snp	A/G	0.0505692	0.150756	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808543	GCCAGAGAACCCACC[A/G]CTAAAGCCGTAGGGT	220441
rs77604481	snp	A/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61818149	ACCAACCTGGCCGGC[A/G]TGGGGGCTCACACCT	220441
rs77680585	snp	A/G	0.0629771	0.165899	intron-variant	RNF152	GRCh38.p7	18:61878472	TCCCAACAAACTCAC[A/G]TGTTAATCACTTGTT	220441
rs77712748	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875454	CAAATTTTTTTTCTT[C/T]GTTCCTACAACCCTT	220441
rs77760802	snp	C/T	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61841104	AAGCTGATCAGAAGT[C/T]AGGCTCGGTCCATTT	220441
rs77764389	snp	A/C	0.0908922	0.192833	intron-variant	RNF152	GRCh38.p7	18:61854178	ACAAGAAGTGTTTTT[A/C]CTTTCACTCAGTTAT	220441
rs77791786	snp	A/G	0.0711525	0.174681	intron-variant	RNF152	GRCh38.p7	18:61864269	TCTGACTGACTGGCT[A/G]TCAGTGGGGTTTCTC	220441
rs77793572	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61872057	ATGTTGGCATCTGCT[C/T]GGCTCTGGGGAGGCC	220441
rs77848152	snp	A/G	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61865440	CCAGGATAAAATTAA[A/G]TATAAAACTCTAAGC	220441
rs77972621	snp	A/G	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61877111	AAGCTTCCAGCCATC[A/G]AAAGACTCATCCACA	220441
rs78038448	snp	C/T	0.0637235	0.166737	intron-variant	RNF152	GRCh38.p7	18:61856392	ACTCATCTGCCACAG[C/T]GCCTACTTCTTTCAT	220441
rs78093143	snp	G/T	0.00953873	0.0683987	intron-variant	RNF152	GRCh38.p7	18:61869593	TCAATAAAGGATGTA[G/T]CAAAGTTTGGCATCA	220441
rs78179423	snp	C/G	0.33875	0.233717	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812970	GAGCAAGAAGACACT[C/G]CAGTGCGAAGTTCAT	220441
rs78194954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859301	GACTGAAGTGAAACA[A/G]GCAACAGAGCGTGAG	220441
rs78230985	snp	G/T	0.0221141	0.102801	intron-variant	RNF152	GRCh38.p7	18:61836123	GATCTTGGTATCTAA[G/T]TAGCATTTCTCACTA	220441
rs78242230	snp	A/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61835250	ATTATTTGCAATAGG[A/G]AAAAAATCTAAATTC	220441
rs78317706	snp	C/T	0.0737376	0.17729	intron-variant	RNF152	GRCh38.p7	18:61842271	AGATTAATTCCACAT[C/T]ATAAACATTTCCTGA	220441
rs78481452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879191	CTCCACTCCGAATGT[A/G]CACAGACTTCTTCAT	220441
rs78524624	snp	A/G	0.0182019	0.0936463	intron-variant	RNF152	GRCh38.p7	18:61882371	TTTGCCTTTTTATTC[A/G]GTGAAGTAATAGACT	220441
rs78530084	snp	C/T	0.0803491	0.183626	intron-variant	RNF152	GRCh38.p7	18:61834266	AAAAGAGAAGGACAG[C/T]ATCCCAAGCTAAGAG	220441
rs78544041	snp	A/G	0.271162	0.249103	intron-variant	RNF152	GRCh38.p7	18:61828481	CCAGGCTGAAGTGCA[A/G]TGACACAATCATAGC	220441
rs78577910	snp	A/T	0.48155	0.0942576	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813282	CTCTCTCTCTCTCAC[A/T]CACACACACACACAC	220441
rs78594378	snp	A/G	0.0785177	0.181917	intron-variant	RNF152	GRCh38.p7	18:61860382	CACGCACCACATAAC[A/G]TTTCGGTCAATAACA	220441
rs78609664	snp	C/G	0.0115144	0.0749975	intron-variant	RNF152	GRCh38.p7	18:61865296	ATATTAAACCCTACT[C/G]AAAAAATGTAAGGTT	220441
rs78623331	snp	C/T	0.0566069	0.158427	intron-variant	RNF152	GRCh38.p7	18:61823901	GAGCCAAGGGCATCC[C/T]GTGCCAGGGGACTCT	220441
rs78629764	snp	A/G	0.0498117	0.149749	intron-variant	RNF152	GRCh38.p7	18:61867794	ACTGAATTCACAGTA[A/G]TCATTTAAAATGTAA	220441
rs78643501	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61843367	AAAAATCTATAGCAA[C/T]AACTGTTGTTTTAAA	220441
rs78689718	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61848421	CAAATATAATCAAAG[A/G]AAAAAAAATCAATAC	220441
rs78691769	snp	C/T	0.0193772	0.0965046	intron-variant	RNF152	GRCh38.p7	18:61870490	TAGCTTGCTGTCCCT[C/T]GAGAGAAGGCTTCAA	220441
rs78717988	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61888577	ATTGTAGGCTAATGC[A/G]CATTTCTGGGCACAG	220441
rs78724106	snp	A/C	0.0733688	0.176922	intron-variant	RNF152	GRCh38.p7	18:61841516	AAGATCTTTCCAACC[A/C]TCATTTCAGACATGA	220441
rs78729893	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879236	CTAAACGATACAGTA[C/T]AACAACAACTTACAT	220441
rs78766006	snp	C/T	0.131723	0.220251	intron-variant	RNF152	GRCh38.p7	18:61826804	TCTAACAGTGGTTAC[C/T]TTACCTGAGTTTTCT	220441
rs78796124	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61878088	GTAGAAAAGGCATCC[C/T]ACTCTGAACTGCATC	220441
rs78820883	snp	C/T	0.0372196	0.131242	intron-variant	RNF152	GRCh38.p7	18:61845451	CGCTGCTCAAACTGA[C/T]TCAGCCACCTGGGAG	220441
rs78833369	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61838407	CCTGTAACCAGAGAC[A/G]GAGGAGTCATACTTA	220441
rs78853062	snp	A/C	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61835998	GAATTTAAATTGGAA[A/C]CATCAGATTACACCC	220441
rs79002370	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61884445	TAGCTTTGCCATTAC[-/AA]AAAAAAAAAAAAGCA	220441
rs79017230	snp	A/T	0.105924	0.204309	intron-variant	RNF152	GRCh38.p7	18:61817938	TCTAGAAAGAATTAC[A/T]CAACCACTATTGCAG	220441
rs79059762	snp	C/T	0.0275645	0.114116	intron-variant	RNF152	GRCh38.p7	18:61891927	GAAAGCCCATTTCCA[C/T]AACCATTCTTATTCC	220441
rs79081276	snp	C/T	0.338976	0.23363	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812994	AGTTCATATCCCCCC[C/T]TTTCTGCAGAATTAC	220441
rs79089280	snp	C/T	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814030	AACCTAATTTCTATT[C/T]TGAGCTTTCAAATAC	220441
rs79092595	snp	C/T	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61844903	TATTCACCTACTCGC[C/T]CCAGTGATTTACGAT	220441
rs79138242	snp	C/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61821172	CCCAAGACCTGCGTA[C/T]CATCATTGGTCAACA	220441
rs79186627	snp	A/G	0.030278	0.119257	intron-variant	RNF152	GRCh38.p7	18:61852932	TTCACTGCCTAATTA[A/G]GAAGCCCTTTTTATT	220441
rs79252543	snp	A/G	0.046775	0.145601	intron-variant	RNF152	GRCh38.p7	18:61856267	AACTAAATGCTGGAG[A/G]ACAAACATAAGCTGG	220441
rs79260375	snp	C/T	0.0425829	0.139564	intron-variant	RNF152	GRCh38.p7	18:61821289	CTATTCCATTTCCAA[C/T]TCTATCCAAGTAAGT	220441
rs79282763	snp	A/C	0.0517044	0.152246	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895847	AGAGGAAGCCCTGTG[A/C]GCCAGTGGGGACTCT	220441
rs79297943	snp	G/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875264	CAATATTCCAGACAG[G/T]GTCCTATATGGAACA	220441
rs79324849	snp	C/T	0.040671	0.13668	intron-variant	RNF152	GRCh38.p7	18:61871892	ACAACTAAAACTACT[C/T]GTGAGGGAGCCTCCA	220441
rs79351067	snp	G/T	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61870308	GATCCCAGCCTCTGA[G/T]GGTGGGATTGATTAC	220441
rs79357898	snp	C/T	0.0193772	0.0965046	intron-variant	RNF152	GRCh38.p7	18:61883758	GCCACAGGAGAAAGG[C/T]GACTCATCTCCTTTA	220441
rs79390252	snp	C/T	0.0689305	0.172377	intron-variant	RNF152	GRCh38.p7	18:61847090	CAAACACCGGTACTC[C/T]TCCCCCATACTTAGT	220441
rs79413535	in-del	-/CCTTTTTTT			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895793	GCATGAGCCACCGCG[-/CCTTTTTTT]TTTTTTTTTTTTTTT	220441
rs79428250	snp	C/G	0.0221141	0.102801	intron-variant	RNF152	GRCh38.p7	18:61865643	CCGTTGTGGAATTTA[C/G]TTTAGAGTCTCTGTT	220441
rs79428439	snp	C/T	0.0718919	0.175435	intron-variant	RNF152	GRCh38.p7	18:61834718	CTGGCTACCAGTATT[C/T]GCAGGCAATTCAGAA	220441
rs79494360	snp	C/T	0.0655868	0.168795	intron-variant	RNF152	GRCh38.p7	18:61864289	TGGGGTTTCTCACAA[C/T]CCCCTCTCCGGTTTA	220441
rs79541383	snp	C/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61836136	AAGTAGCATTTCTCA[C/G]TAAAAAGAAGCTGAC	220441
rs79556987	snp	G/T	0.130008	0.219321	intron-variant	RNF152	GRCh38.p7	18:61886201	GGAAGCTCTTAAAAA[G/T]AAGTTTCTATCTTCT	220441
rs79569450	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61857449	CCTCAGAATAGTCTA[C/G]TTTGAATCCTGGCAG	220441
rs79605325	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61873105	CAATCTTGAGCAAGC[C/T]ACTAAAGTTCACTGT	220441
rs79690519	snp	C/T	0.0298908	0.118541	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808167	AAGACACCAGTTTGG[C/T]ATACAAAAATACCAT	220441
rs79726000	snp	C/T	0.174932	0.238463	intron-variant	RNF152	GRCh38.p7	18:61857981	ATGGGTTTAGCTTTA[C/T]GTTTGGGTCTCCTCT	220441
rs79784366	snp	C/T	0.162909	0.23434	intron-variant	RNF152	GRCh38.p7	18:61836997	GATAAAGAGAGTTAT[C/T]TTTACAGATATCACC	220441
rs79800814	snp	A/T	0.0832709	0.186283	intron-variant	RNF152	GRCh38.p7	18:61824431	ATTCTATGCTTCTCA[A/T]CCCTGACAGATCATT	220441
rs79849839	snp	A/C	0.0166325	0.0896639	intron-variant	RNF152	GRCh38.p7	18:61836862	CATTTTACCATCTCC[A/C]ATGTAATGACCAATT	220441
rs79857151	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61878159	GGCCCCACCTAGGTA[C/T]AGAAAGTAGTATAGT	220441
rs79890317	snp	C/G	0.141258	0.225111	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814316	TCCTTCACTTCCCCC[C/G]ACCCTCCTCACCATT	220441
rs79900838	snp	G/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61853317	TTTTTTTTTTTTTTG[G/T]AGACAGGTTACCCAG	220441
rs79913974	snp	C/T	0.0659589	0.169201	intron-variant	RNF152	GRCh38.p7	18:61843498	GATGAGATATTTCTA[C/T]ATCCATGTTCATAGC	220441
rs79951105	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61871416	ATCAAGTTACCAGGA[C/T]TCATCATCTCCATGA	220441
rs79951917	snp	A/G	0.0138799	0.0821421	intron-variant	RNF152	GRCh38.p7	18:61892071	CCCCAGATCTGGCTA[A/G]GCTGACATCAAAACA	220441
rs79954757	in-del	-/AAA			intron-variant	RNF152	GRCh38.p7	18:61884456	TTACAAAAAAAAAAA[-/AAA]GCAGAAAACCAAATT	220441
rs79978522	snp	A/G	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61867950	AATTTAACCTTAAAC[A/G]AATATGCTAGCTAAC	220441
rs79991965	snp	C/G	0.106278	0.204558	intron-variant	RNF152	GRCh38.p7	18:61818705	GTAGGATATAAATCA[C/G]ACCCAGATTCTACCC	220441
rs80046594	snp	A/G	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61872425	AGACTAACAATGCTT[A/G]TTTAAAAATCTTACT	220441
rs80074665	snp	A/G	0.0217236	0.101931	intron-variant	RNF152	GRCh38.p7	18:61852324	TTTTTAAAAACCTCT[A/G]GGCAACAAGAGGAGA	220441
rs80114471	snp	C/T	0.105924	0.204309	intron-variant	RNF152	GRCh38.p7	18:61824186	ATCTGCCAATCATTA[C/T]TATTAGGAATCAGGA	220441
rs80158845	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF152, LOC105372159	GRCh38.p7	18:61894363	CCCTTCGGGCGGCAC[A/C]CCCACCTGCCCGGCC	220441
rs80235039	snp	C/T	0.084728	0.187577	intron-variant	RNF152	GRCh38.p7	18:61839179	ACTGCAGTACAGTCA[C/T]TAAAATCGGGAAATC	220441
rs80238164	snp	A/G	0.0486741	0.148216	intron-variant	RNF152	GRCh38.p7	18:61882046	CAAATTCAAACATCC[A/G]AAATCCGAAATGCTC	220441
rs80253952	snp	A/T	0.0178098	0.0926698	intron-variant	RNF152	GRCh38.p7	18:61881279	TGTATTTAGCTGTTA[A/T]GTACTATAGATTATA	220441
rs80265400	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890209	CTGAGCTAGGTCCCA[C/T]AGGACACACTTTCTA	220441
rs80272523	snp	C/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875635	AACTCTTAATTTCTC[C/T]CAAATCTGTTTTTTT	220441
rs80297291	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61861054	CTTTATAAACTTTTT[A/T]AATTTTTTAAAACTT	220441
rs80342772	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61865354	TTTCAAAATGAATTA[A/G]TAGTTCTCTGGGTTT	220441
rs111241934	in-del	-/A	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811048	GATTAGTATCTTGGC[-/A]AAAAAAAAAAAATTA	220441
rs111267255	snp	C/T	0.077417	0.180873	intron-variant	RNF152	GRCh38.p7	18:61859126	ACCACCATTCAGATG[C/T]CACTATGCACTTGTT	220441
rs111436184	snp	C/G	0.255782	0.249933	intron-variant	RNF152	GRCh38.p7	18:61823535	AACTCCTGACTTCAA[C/G]TGATCTGCCCGTCTC	220441
rs111443012	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810426	CGAGGCGGGTGGATC[A/G]CCTGAAGTCAGAAGT	220441
rs111451798	in-del	-/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61876704	CTCTCTGTGCTTCAA[-/T]TTCCTCACCCATATA	220441
rs111457024	in-del	-/AGG	0.388775	0.207946	intron-variant	RNF152	GRCh38.p7	18:61830763	AAGAGCTGAGAGTGA[-/AGG]AGGAGTATAGAAAAG	220441
rs111488589	snp	A/C	0.203575	0.245652	intron-variant	RNF152	GRCh38.p7	18:61819857	GAGACTCTGTCTCTA[A/C]TAAAAATAAAAAAAT	220441
rs111505725	snp	A/C	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61849329	TTTTTGCTACCTTGA[A/C]GTTAACCCTGAGGAA	220441
rs111542081	in-del	-/TGATTTCTA	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61856171	ACAAAATTCACTGGC[-/TGATTTCTA]TGATTTCTATCTGAA	220441
rs111554126	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844222	GAAGGAGGGAGGGAA[A/G]GAGGGAGACGGGAGG	220441
rs111559884	snp	A/T	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61890764	TGCTGACAGCATAGG[A/T]GGGTTCAAACAACTC	220441
rs111581811	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61843449	GCAATTCCACCTCTG[A/G]GTATTTACCCTAAAA	220441
rs111584642	snp	A/G	0.117188	0.211804	intron-variant	RNF152	GRCh38.p7	18:61868445	CGGGTGCAGTGGCTC[A/G]TGCCTGTAATCCCAG	220441
rs111590179	snp	A/G	0.141258	0.225111	intron-variant	RNF152	GRCh38.p7	18:61851421	AACACTTACCCAAGC[A/G]CCTGAGCTGCCCCAG	220441
rs111603571	in-del	-/A	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815385	GGTTTCAATAAAAAG[-/A]AAAAAAAAAATAAAG	220441
rs111641999	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61888765	GGAGTCAGACTGCTG[A/G]ATCACACAGTGTAAC	220441
rs111670441	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857504	TAAAAATGGCTTTTT[C/T]TCTTCAAACAGCAAC	220441
rs111694610	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61862164	TTTTTACATGTTAAT[A/G]CAAAGCCCTGCCTCC	220441
rs111697787	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61878349	GAATTATCCAGCCCC[A/G]GAGGTCAAAATGCTG	220441
rs111697878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866257	TCTAGACAGCGAGTC[A/G]GGCCCAGGTAGCCCC	220441
rs111709772	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61824453	CAGATCATTTACAAA[C/T]ATTATCTGTTAGTGA	220441
rs111761614	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61819066	AGGAAAGAAGGTAAG[C/T]GATTACAGAATTATT	220441
rs111799444	snp	A/G	0.0325976	0.123435	intron-variant	RNF152	GRCh38.p7	18:61881752	AGAATGTTATTTTAA[A/G]GAGCACAAAGAGAGG	220441
rs111800419	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896023	TATCAGTTGTCCCTG[A/G]GATCCCAATTAAAAC	220441
rs111801758	in-del	-/AAAC	0.188016	0.242194	intron-variant	RNF152	GRCh38.p7	18:61857695	GACTCACCAGTCATT[-/AAAC]AAACAAACAAACAAA	220441
rs111824920	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61876324	AACCTTCTAAAGGAG[C/T]ATCTTGGTATAAAAA	220441
rs111843195	snp	C/T	0.0402882	0.136092	intron-variant	RNF152	GRCh38.p7	18:61848962	CACAAACCAATAGCC[C/T]GTGGAGATCCTGGAC	220441
rs111850940	in-del	-/GAGA/GAGAGA/GAGAGAGA	0.410274	0.272198	intron-variant	RNF152	GRCh38.p7	18:61829597	AGAGAGAGAGATAAG[-/GAGA/GAGAGA/GAGAGAGA]GAGAGAGAGAGAGAG	220441
rs111861215	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61852753	TTTAAAAGCTCTCCA[C/G]GTGACTCACTGAGCA	220441
rs111871157	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61848501	GAATAGCAAGCAACA[A/T]CCGTAAACTTACTAC	220441
rs111880144	snp	A/C	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812748	TTTTAAAAATTCAAA[A/C]CACATGGTTTGATAG	220441
rs111901070	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61863386	GTTGCAGTGAGCGGC[A/G]ATCGTGCCACCGCAC	220441
rs111906467	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61827187	TGTTCCTTTGCATAG[C/T]TATAGCAGGCCACAA	220441
rs111969460	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61865789	AGGCAAATATTCCCA[A/T]GACAGCTGTCCCAAT	220441
rs112031350	snp	A/G	0.0399052	0.1355	intron-variant	RNF152	GRCh38.p7	18:61879953	CAGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA	220441
rs112068458	snp	A/G	0.5	0	downstream-variant-500B	RNF152	GRCh38.p7	18:61807738	AGTTGTTCTGTATAC[A/G]GTGCAACAAGTTGTT	220441
rs112094129	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61884789	GTCTTGAACTCCTGA[C/T]TTCAGGTGATCTGCC	220441
rs112273721	in-del	-/CTTT	0.32955	0.237006	intron-variant	RNF152	GRCh38.p7	18:61828248	GTTTTTTCTTCCTTC[-/CTTT]CTTTTTTAAGAGACG	220441
rs112290516	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61865017	AAGAGGGAAACTCCA[A/T]CTCAAAAAAAAAAGG	220441
rs112296907	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61856393	CTCATCTGCCACAGC[A/G]CCTACTTCTTTCATG	220441
rs112308991	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61845988	TATAAAATAAGTCCA[A/G]GGGAGCTCACTTATC	220441
rs112315982	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61880699	GATAAATTTCCATGT[C/T]ATTTTGTAAAACATT	220441
rs112336633	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61820048	AAAAAAAAAGAATCC[A/G]GCCGGGCATGGTGGC	220441
rs112382337	snp	G/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	RNF152, LOC105372159	GRCh38.p7	18:61894643	CGCTCCCTCGGCTTT[G/T]CCCCCAGTGCCTACC	220441
rs112384554	snp	C/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61866457	ACATCCACACTCTCG[C/G]CCGCGTTTCTGTGCT	220441
rs112399911	snp	G/T	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61877767	CTGTCCCTTTTTTTG[G/T]GTTTGGAATCTCTAT	220441
rs112470390	snp	C/T	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61846744	AAGAAGCACCAGACA[C/T]AGAATTATTAATACT	220441
rs112471489	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61853616	CTTTTTTAGCTGCCA[C/G]TGGCTGCCTGCATTC	220441
rs112471807	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61849806	TCCTGGCCTCAAACC[A/G]TCCTCCCGCCTCAGC	220441
rs112477547	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61832051	CTTGAACTGGTTTTG[C/T]TGGAGTCGTTGCAAT	220441
rs112477696	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61820753	AACCTTCTTTCTTTC[C/T]ATACTATTTACCTTA	220441
rs112484531	in-del	-/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61853601	CACCGGTTCCTTACC[-/T]TTTTTTAGCTGCCAG	220441
rs112622414	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61867462	ATCTCAAAAAAAAAA[A/G]AGAGATGACAAACTG	220441
rs112627330	in-del	-/AACA	0.412735	0.189782	intron-variant	RNF152	GRCh38.p7	18:61831681	CTACCCTCAAAGCAG[-/AACA]AACAAACAAACAAAC	220441
rs112639447	snp	C/G	0.0569829	0.158885	intron-variant	RNF152	GRCh38.p7	18:61891019	AGTTAATTAGAATCA[C/G]GTCTTCCTATAGGGA	220441
rs112720047	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61833506	TTTAATTGTCGAAAC[C/T]CCTCTGCGTTTCCCT	220441
rs112739957	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61819495	AGTGAATAGTGATGA[C/T]TAGGACAGAATGATG	220441
rs112749574	snp	A/G	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61874443	CAATCAACCAACCAG[A/G]ACCACTGAAGAAATC	220441
rs112784334	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61836573	AGAAGGTTCCCACCC[A/G]AATCTGACCATGTTC	220441
rs112797020	snp	A/C	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61881784	TTTAGCATCTCCACG[A/C]ACAAGTTCTACAAAT	220441
rs112803661	snp	C/T	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61873877	CAGATCTTAGCTAAT[C/T]GGTACTAATTACTGG	220441
rs112860853	snp	A/G	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61883286	TACCGGGCCCCAAGC[A/G]GCTACCCCTTTTTAA	220441
rs112866449	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61889425	GTGAACAAAGATATA[C/T]GAGTGAACAGCTCTT	220441
rs112896113	snp	G/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61837818	TTTCTATTTTGCACA[G/T]ACAAAGTGTCTAGCA	220441
rs112943924	snp	C/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894783	GGGGGCCGGGGCCGC[C/G]GTGGGTGGGTTGGGG	220441
rs112963217	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61881438	GTCTGTTCAGAACTG[C/T]TTCCTCTGATGGGAA	220441
rs113025132	snp	C/T	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61877497	ATACATAAATTGCCA[C/T]AAATATCTCAACTCG	220441
rs113027324	in-del	-/T	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811738	GGGATTTCATTAGGC[-/T]TTTTTTTTTCCTGTA	220441
rs113112635	snp	C/T	0.5	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813317	ACACACACACACACA[C/T]ACACAAGAATGCACA	220441
rs113123737	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61866819	CACCGCTGAGCAGCA[C/T]ATGACAAGACAGCCC	220441
rs113141135	snp	C/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61826571	ATATAAACTTTTTTT[C/T]CTCTTTACATGTTTT	220441
rs113177131	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61885982	TTTGCTTTCTTTTGC[A/T]TTCTTTTTTTTTTTT	220441
rs113227067	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810517	GCTGGGCATGGAGGC[A/G]CATGCCTATAATCCC	220441
rs113248720	in-del	-/C	0.0142736	0.0832652	intron-variant	RNF152	GRCh38.p7	18:61861915	ACATCTCCTATTAGG[-/C]CCCGACCTCCAACAT	220441
rs113258367	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61859880	ACTCCACCTCAAAGA[A/G]AAAAGAAAAGAAAAG	220441
rs113286440	snp	A/G	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61890851	ATGGAATTCAGCTAA[A/G]AAGACTACAATGAAA	220441
rs113312664	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61860387	ACCACATAACGTTTC[A/G]GTCAATAACAGATCA	220441
rs113343948	snp	G/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61836257	GGGGACATGTCAAAA[G/T]GCCCCAGGAGCCAGC	220441
rs113345113	snp	C/T	0.0850919	0.187897	intron-variant	RNF152	GRCh38.p7	18:61857160	CTGACTTGCATTATA[C/T]GTCAGGGTTCAAGCT	220441
rs113366616	snp	A/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61873746	ATTGTTCAAAAGTCC[A/G]TTATGAACATCAGTT	220441
rs113426267	snp	G/T	0.0763149	0.179815	intron-variant	RNF152	GRCh38.p7	18:61858612	TCGACTTCCACTCAG[G/T]GTTCCCACCAAGCCA	220441
rs113443351	snp	A/G	0.0626037	0.165477	intron-variant	RNF152	GRCh38.p7	18:61891912	CCTACAAGAAAAATC[A/G]AAAGCCCATTTCCAT	220441
rs113553153	snp	A/G	0.41325	0.18934	intron-variant	RNF152	GRCh38.p7	18:61844223	AAGGAGGGAGGGAAG[A/G]AGGGAGACGGGAGGG	220441
rs113558082	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61847083	TGCTCAGCAAACACC[A/G]GTACTCCTCCCCCAT	220441
rs113590133	snp	A/G	0.5	0	synonymous-codon	RNF152	GRCh38.p7	18:61816176	CATGTAGCACCCATT[A/G]CTGGGAAGTTTGATG	220441
rs113592622	snp	A/T	0.0803491	0.183626	intron-variant	RNF152	GRCh38.p7	18:61832002	AATAAAATCCAATTC[A/T]TTTTCTTGAAACTAA	220441
rs113631631	snp	A/G	0.416545	0.186448	intron-variant	RNF152	GRCh38.p7	18:61844221	GGAAGGAGGGAGGGA[A/G]GGAGGGAGACGGGAG	220441
rs113665879	snp	A/C	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61871209	CCCACCCACCTCCCC[A/C]CACCCCAAAAAAAAA	220441
rs113673174	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61853559	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCTGA	220441
rs113674285	snp	C/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61851507	GCCTTATCTCATCCT[C/T]ACAACAGCCCTATGG	220441
rs113676454	snp	A/G	0.0142736	0.0832652	intron-variant	RNF152	GRCh38.p7	18:61883270	CTGAGTGTCTACTGT[A/G]TACCGGGCCCCAAGC	220441
rs113691864	snp	A/G/T	0.00358779	0.0422022	upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894471	GGCACCAAAGGGGGT[A/G/T]GGGGGAGAGGCTGGG	220441
rs113699610	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858891	AAGTTTGGTCAGCAA[A/C/G]CCTGAGACAAAACAA	220441
rs113778872	snp	C/G	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61879920	CAGTGAGCCGAGATC[C/G]CGCCATTGCACTCCA	220441
rs113809350	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61886125	CCAAACATTGGTATA[C/T]GTACTGCAGCCTGGT	220441
rs113834567	snp	A/G	0.0562307	0.157967	intron-variant	RNF152	GRCh38.p7	18:61892014	GGAGTGTCCTGCTAA[A/G]TCTGAAGGTTACGTT	220441
rs113858363	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61831922	ATAGTATTATGTGTG[G/T]GGGGGGGTGTGGGTG	220441
rs113872355	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811471	TCTTCAACTCTTTCA[A/G]GGATAACTGAAATTT	220441
rs113895454	snp	C/G	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61866101	GGCCATATACTCCCA[C/G]CTCCAAGGGAATTTG	220441
rs113913200	snp	A/T	0.5	0	intron-variant	RNF152	GRCh38.p7	18:61856498	GATGCAAATCCCATA[A/T]AAAGGGTCATAGCTA	220441
rs113974330	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61849881	CATCATCAAATGAGT[C/T]TGAGGAGCACCTGGC	220441
rs114049380	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61872193	CGTGAGAACTCTATC[A/G]GGAGAACAGCACCAA	220441
rs114133247	snp	A/G	0.00716266	0.059414	intron-variant	RNF152	GRCh38.p7	18:61829472	CAGAGAGCAAAACAA[A/G]GCCCAGGGAGAGAGG	220441
rs114174434	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896136	AAAGCTGTATCCATG[C/T]TTTAGAAGCCTAAGG	220441
rs114184534	snp	C/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61837473	TATTCCAGGGTAAAA[C/T]GTCATGATGTCTGCC	220441
rs114197428	snp	A/C	0.0185938	0.0946107	intron-variant	RNF152	GRCh38.p7	18:61885601	GCGTGAGCCACCACG[A/C]CCAGCCGAGAGCGTT	220441
rs114355576	snp	C/T	0.0197687	0.0974348	intron-variant	RNF152	GRCh38.p7	18:61881113	GAGATAGGGTTTCCT[C/T]ATATTAGTCAGGCTG	220441
rs114368113	snp	C/G	0.089084	0.191327	intron-variant	RNF152	GRCh38.p7	18:61866896	CTTTAAAAAGCAAAA[C/G]AACACAAAAAAAACA	220441
rs114443773	snp	C/T	0.0256215	0.110247	intron-variant	RNF152	GRCh38.p7	18:61829820	ATGGAAGAGAAAGAC[C/T]AGTCCCCTCCTATTC	220441
rs114501728	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874518	CACAGTCCTTAAGGA[A/G]GCAGAACTAGTAAGA	220441
rs114508807	snp	C/T	0.0711525	0.174681	intron-variant	RNF152	GRCh38.p7	18:61873962	AGGAAAAGTAAACCC[C/T]TTGCATCCTCTAAAG	220441
rs114528401	snp	C/T	0.0494327	0.149241	intron-variant	RNF152	GRCh38.p7	18:61864784	CGGGCACAGTGCTCA[C/T]GCCTGCCGAGGCAGG	220441
rs114618405	snp	A/G	0.0111196	0.0737302	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816530	TTCTCAGAGGCCACC[A/G]CCCTGTGTCTTTGCA	220441
rs114685014	snp	A/G	0.0520825	0.152737	upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894519	CCGCCCTCCCCGGCG[A/G]CTCCACCCCCTCCTC	220441
rs114747183	snp	G/T	0.0150606	0.0854603	intron-variant	RNF152	GRCh38.p7	18:61889141	TCCCAATTCAGAAAC[G/T]CTTTGGGTGCTACAT	220441
rs114815191	snp	C/T	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61872061	TGGCATCTGCTCGGC[C/T]CTGGGGAGGCCTCAG	220441
rs114873950	snp	A/C	0.0352966	0.128072	intron-variant	RNF152	GRCh38.p7	18:61862681	CCCACGTGTCTCTTC[A/C]TCGGTATCCTTTGCA	220441
rs114879065	snp	A/G	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61868658	CAGTGAGCCAAGATC[A/G]CCCATTGCACTCCTG	220441
rs114929767	snp	C/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61830359	TCATCCCAAACAGAA[C/T]TCCATACTCATTCAA	220441
rs115076343	snp	A/G	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61859364	TGCTTCAGAAACGTC[A/G]CATCAGTTTCACACA	220441
rs115106041	snp	A/G	0.021333	0.101051	intron-variant	RNF152	GRCh38.p7	18:61877292	ACTGAATTTAGTCTG[A/G]TAAGCAAGTTCTTGG	220441
rs115145233	snp	C/T	0.0667028	0.170006	intron-variant	RNF152	GRCh38.p7	18:61844231	AGGGAAGGAGGGAGA[C/T]GGGAGGGGAGGGGAG	220441
rs115202821	snp	C/T	0.0788843	0.182262	intron-variant	RNF152	GRCh38.p7	18:61835208	CACAGTACAAAATAG[C/T]ATATTTACAAGGTAA	220441
rs115240843	snp	A/G	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61854846	TCTGTGTTCAACCTG[A/G]CGTGAAAATAGCAGG	220441
rs115277081	snp	A/G	0.0170251	0.090679	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812148	ACCCAGAACTGCATC[A/G]TTCAATATGGCAGCC	220441
rs115395605	snp	C/T	0.0185938	0.0946107	intron-variant	RNF152	GRCh38.p7	18:61856466	AAGGAAGGGAGGGGA[C/T]GGGAAGACAGTCTTG	220441
rs115432255	snp	C/T	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61863482	CTTTTTTCAGTTGTT[C/T]AGGTAACATCACTGT	220441
rs115433550	snp	G/T	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61879274	GTGTTTACATTTACA[G/T]CATGTTTACATTACA	220441
rs115452639	snp	A/G	0.00131348	0.0255933	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815845	AGAGACTTCCCTGCA[A/G]CCCTCTTCAGCCACA	220441
rs115468669	snp	A/G	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61867596	TTCATTTTAAGGAGG[A/G]AGAGCACCCACTATT	220441
rs115497950	snp	C/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61855851	GGCCACAGAGGTTTC[C/T]GGCTGGTGACTCCCA	220441
rs115498001	snp	A/T	0.021333	0.101051	intron-variant	RNF152	GRCh38.p7	18:61835620	AATAAATTAAAAAGG[A/T]TAAACAAAATCAAAC	220441
rs115506416	snp	A/G	0.00953873	0.0683987	intron-variant	RNF152	GRCh38.p7	18:61827693	CTCTACCTACCCTCA[A/G]TATTGATGATTCATG	220441
rs115644815	snp	C/T	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61864780	TGGTCGGGCACAGTG[C/T]TCACGCCTGCCGAGG	220441
rs115670953	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892658	ATTTCTTTGAACCAG[A/G]AGTTTTAGCAGCCCC	220441
rs115676976	snp	A/G	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61817173	GCAGAAGAAGCACAC[A/G]AAGGCATCTTTCATC	220441
rs115735859	snp	C/T	0.00914312	0.0669923	intron-variant	RNF152	GRCh38.p7	18:61816765	ACGCCCAGTGAAAGG[C/T]GAATGAAAGTTGTCT	220441
rs115827531	snp	C/T	0.0232847	0.105357	intron-variant	RNF152	GRCh38.p7	18:61877602	TACTGAAAGTATTTA[C/T]AGCTCAAAGCTGCTT	220441
rs115831643	snp	A/G	0.0158469	0.0875917	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896418	TTTTATTTTTGTAGA[A/G]ATAGGGGTCTCTCTT	220441
rs115864975	snp	A/C	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61836029	ATGATTTAAAATAAT[A/C]CATAAATTTCTAAGC	220441
rs115865008	snp	A/G	0.0225045	0.103662	intron-variant	RNF152	GRCh38.p7	18:61882064	ATCCGAAATGCTCCA[A/G]AATCAGAAACTTTTT	220441
rs116009255	snp	C/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61857095	AGGCAGGGGAACAGG[C/T]ATAAAAGACACAGAA	220441
rs116135839	snp	C/T	0.0189856	0.0955633	intron-variant	RNF152	GRCh38.p7	18:61888423	ATGGTGTGAAAACAA[C/T]ACACATTCAGTAGAA	220441
rs116279781	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61878749	GAAGAAATGGAAGGG[C/T]CTGGCAGTTCTCTGA	220441
rs116300105	snp	A/G	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61833814	ATAGATCTAGAATGG[A/G]GTGATACATCACCTA	220441
rs116307326	snp	G/T	0.0912534	0.193131	intron-variant	RNF152	GRCh38.p7	18:61864739	ATCTCATTAGCATAA[G/T]CCAAGGTATGGTTGA	220441
rs116595510	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880913	TCTCTCTCTAGTTTT[C/T]TTTTTTTTTTTTTTT	220441
rs116682221	snp	A/G	0.106278	0.204558	intron-variant	RNF152	GRCh38.p7	18:61818308	AGCACCTCTAGTCCC[A/G]GCTACTCAGTAGGCT	220441
rs116694306	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61869778	ACACATGCACACACC[C/T]GGAAGCTTATCATCT	220441
rs116710395	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61860030	AACATGACTAGTGTC[C/T]TTTAATACAGAAAAG	220441
rs116777983	snp	A/T	0.0221141	0.102801	intron-variant	RNF152	GRCh38.p7	18:61880279	CAAAATTGTCCATCT[A/T]TGTTCCCAAAGACAG	220441
rs116886631	snp	G/T	0.0889698	0.191231	synonymous-codon	RNF152	GRCh38.p7	18:61816275	CTGCGACACGGAGAA[G/T]CCGGGAGGCAGCTTG	220441
rs116981748	snp	C/T	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61841373	ATTCATGAAATAGTC[C/T]CTTCTCCATTAATAA	220441
rs116983854	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61869600	AGGATGTAGCAAAGT[C/T]TGGCATCAAGAACTT	220441
rs116984814	snp	C/T	0.0633504	0.166319	intron-variant	RNF152	GRCh38.p7	18:61824721	AGGGGGTCCCAACAA[C/T]GCTACCTTGAAAAGA	220441
rs117081940	snp	C/T	0.0379877	0.132479	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813688	CTGTACAGAAACATA[C/T]GCAGATATCACTCAC	220441
rs117083278	snp	A/G	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61827022	TCTTCATTCTTTGAA[A/G]TATGGATCTATTATT	220441
rs117168821	snp	A/T	0.0236746	0.106192	intron-variant	RNF152	GRCh38.p7	18:61854457	GTAACACCGGTGTCT[A/T]CCATGTTCAACACAA	220441
rs117193631	snp	C/T	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61816848	TCCAATAGTTGTAGA[C/T]GATGCATCTGTATTT	220441
rs117234340	snp	A/G	0.0263992	0.111815	intron-variant	RNF152	GRCh38.p7	18:61862783	CATCAAAGCCAAAGC[A/G]GGGGTTCTGGGGACC	220441
rs117301234	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809122	GTTTTGCAGCTATAC[C/T]CTTCCTTTATTAAGT	220441
rs117374684	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61869985	GACAGAGGCTTTTAC[A/G]TTGGGCTTGTTGACT	220441
rs117399583	snp	A/G	0.0425829	0.139564	intron-variant	RNF152	GRCh38.p7	18:61853353	AGTGTAATGGCACAC[A/G]ATCACAGCTCACTGC	220441
rs117415869	snp	C/T	0.0693013	0.172766	intron-variant	RNF152	GRCh38.p7	18:61844968	TCATTTTATTCCTTC[C/T]ATTCCTCCTGAGGGC	220441
rs117456246	snp	C/T	0.0693013	0.172766	intron-variant	RNF152	GRCh38.p7	18:61848638	AAGGGTCCTACAAGG[C/T]CCCCAGAGACCAGCA	220441
rs117460951	snp	C/G	0.00835141	0.0640778	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811611	TACAACGACAAGCTG[C/G]CCAACTTCAAGGGCA	220441
rs117502517	snp	C/T	0.0726307	0.176182	intron-variant	RNF152	GRCh38.p7	18:61833612	TAACATAACTGAACA[C/T]GAGGGCCGTCTGTTA	220441
rs117509918	snp	A/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61885723	TTTGAGTATCAAAGA[A/G]GAGTTTCTATCATGT	220441
rs117541630	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816739	AGTCTTGAGACTACA[G/T]GATTCCCATAACGCC	220441
rs117559360	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61876234	TTCTGAATCCTCTGA[A/T]TTCCACTACCATTTC	220441
rs117616449	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876032	CTTTCCAATCCTTTT[C/T]CATACTATTCCTACT	220441
rs117665940	snp	A/G	0.0368353	0.130617	intron-variant	RNF152	GRCh38.p7	18:61818895	CTGGCCTAGAGATGG[A/G]AGCGCTAAGTACTTA	220441
rs117712351	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61836331	AAAAAAAGTGCTATA[C/G]GCCGAATGTCTGTGT	220441
rs117830723	snp	C/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61883913	GAAAGCTTTACAGAC[C/T]TTCAAACCAAAGACT	220441
rs117878853	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61859249	CTTTTGTCCTTCCCA[C/T]GGGTACCATCAAAGC	220441
rs117993683	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61867143	TGGGAACTCAAGAGT[C/T]ACCCATGCATGGCAA	220441
rs118016783	snp	A/G	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61886996	GATGATAGGATAGAG[A/G]CAGAGGAAGGAAGAG	220441
rs118039256	snp	C/G	0.0170251	0.090679	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810180	CAGTTAAGAAATTAG[C/G]ATCTAATCCAATATT	220441
rs118054266	snp	C/T	0.0193772	0.0965046	intron-variant	RNF152	GRCh38.p7	18:61889563	TTAGAACTCACCACC[C/T]TCCTAGTCAATACAG	220441
rs118064738	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61876801	TAAGCAAAACCCTTA[A/G]AGCCTGGCACACAAT	220441
rs118090509	snp	C/G	0.0629771	0.165899	intron-variant	RNF152	GRCh38.p7	18:61819744	TCAAAGAGAAGGTCA[C/G]GCACAGTGGCTCACG	220441
rs118109648	snp	A/C	0.00874735	0.0655527	intron-variant	RNF152	GRCh38.p7	18:61881916	GACTGCCTTGAGATG[A/C]AATTCTTAAATAACT	220441
rs118136768	snp	C/G	0.0681886	0.171594	upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894455	GTGTCACTGAGACTC[C/G]GGCACCAAAGGGGGT	220441
rs118181257	snp	C/T	0.0887219	0.191022	intron-variant	RNF152	GRCh38.p7	18:61853814	TTCCTTGAAGTCCCT[C/T]TTGCCATGTAGGTAA	220441
rs137859887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61892230	TCTCTGTTCTCTTTC[C/T]GCTGCCCCCAACAGC	220441
rs137889582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827535	TTCCTCAAATTACCC[A/G]GAGAACATTCTATAT	220441
rs137935150	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61860188	AGTGCATGGGCCTGC[C/T]GACACCATGCCTGTG	220441
rs138007770	in-del	-/A	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810731	TTTAAATAGACTACT[-/A]ACTTTCAAAACAGCT	220441
rs138068716	snp	A/C	0.00874735	0.0655527	intron-variant	RNF152	GRCh38.p7	18:61888525	ATATTTGATGCTTTA[A/C]TACAAAATAGGCTTC	220441
rs138084326	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855843	GTGCCATTGGCCACA[G/T]AGGTTTCCGGCTGGT	220441
rs138173938	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876823	GCACACAATTCATGG[C/T]GTAAGTGTCAGTCTT	220441
rs138187760	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808826	CTAGAGTCTGTCTGC[A/C]CTGACGTGGCAACCA	220441
rs138213335	snp	A/C	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61883194	CTCTTGCACTTCTCT[A/C]TGCAGCTTTCAAAAA	220441
rs138214848	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884081	TGAGCCCAATGATTG[A/G]TGGATGGTAGATGCT	220441
rs138225766	snp	A/C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815684	GTATCTTGTTGAGAC[A/C/T]GCACCTTCTGCCCTT	220441
rs138226482	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812286	TGCCTGGTGGCTACC[A/G]TACCAGACGGCACAG	220441
rs138277596	in-del	-/AAAAAAC			intron-variant	RNF152	GRCh38.p7	18:61872787	GGTATAGAAACAAAA[-/AAAAAAC]CAGCCATAATAAGAT	220441
rs138335732	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872657	ATTCTACTGTAGTGG[A/T]CTTCCCTCAAAATAA	220441
rs138344513	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841952	ATTGACAATACGTAA[C/T]AAATGGACATGACTG	220441
rs138383704	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815097	TCTTATTTTGTGAGA[C/T]GGCTTGAGGAAAATC	220441
rs138440399	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61870914	ATCAGTTCAGCCCAG[C/T]TGTCTAGATAATGTG	220441
rs138441250	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61828343	TGCATCCTTGAACTC[C/T]TTGCCTCAAGCAATC	220441
rs138445890	snp	C/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61824139	TGTCAGTATTGCAGT[C/G]AGTGATGATAACTAC	220441
rs138454336	snp	C/T	9.90246e-05	0.0070358	synonymous-codon	RNF152	GRCh38.p7	18:61816254	GACCTCCGGGTCGTC[C/T]GGGAGCTGCGACACG	220441
rs138504642	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859650	TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAA	220441
rs138553749	snp	G/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868079	CTGAGGAGATTCATG[G/T]TAATGTGTGCAGCTG	220441
rs138572818	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893105	ACAGGATAAATAACC[A/T]CCTCCCCCCTCCTCC	220441
rs138601442	snp	A/G	0.0107246	0.0724382	intron-variant	RNF152	GRCh38.p7	18:61856293	GCTGGAAAATGACAC[A/G]GGGAAATACACGATG	220441
rs138638221	snp	C/T	0.135484	0.22223	intron-variant	RNF152	GRCh38.p7	18:61820323	GACAGAGAGAGACTC[C/T]GTCTCACCAAAAAAA	220441
rs138644071	snp	C/T	0.0107246	0.0724382	intron-variant	RNF152	GRCh38.p7	18:61888840	CCTTTCCGGTTTCCA[C/T]GACGTCACAATGGGC	220441
rs138777320	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61855286	AGTCAACCTTAAAAG[C/T]TTAATAAAATCAGGA	220441
rs138796502	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61851668	CTGTCTGGACACCCA[A/T]ATTCACCCAGGGCAA	220441
rs138799418	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812722	GAGGTTTGGACACCA[A/G]TGTTTTACAATTTTA	220441
rs138817006	in-del	-/TTTT	0.483852	0.0883933	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896218	GGGCAGGAAGGAGAA[-/TTTT]TTTTTTTTTTTTTTT	220441
rs138836931	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812517	GTTGCCTTTTCATCA[C/T]AACTTATGCCCCAAG	220441
rs138853604	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877019	GGTATGGTGAAACTC[A/G]GTTGGGGTGGCTCTT	220441
rs138864168	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863911	ATAAGGAACTTGGGT[C/G]GTGAGCTCCCGCTCT	220441
rs138959927	snp	A/T	0.00914312	0.0669923	downstream-variant-500B	RNF152	GRCh38.p7	18:61808050	AGGAGGGGGGAAAAA[A/T]CCAATACGTGAGTCT	220441
rs138966910	snp	C/T	0.02016	0.0983543	intron-variant	RNF152	GRCh38.p7	18:61851924	TCATTGAAAATATAA[C/T]GACATCTGCACAGTA	220441
rs138968144	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876446	AGTTGAGAAAGTACA[C/T]TCAGCCCACAAAAAA	220441
rs139008921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847516	AAGGGAAAATATAGG[C/T]ATTGCATATTCTGCC	220441
rs139079821	snp	C/T	0.000153988	0.00877328	missense	RNF152	GRCh38.p7	18:61816216	GTGTGTTCGGAAGTG[C/T]GTGGAATGGCGATGA	220441
rs139123137	snp	C/T	4.95062e-05	0.004975	missense	RNF152	GRCh38.p7	18:61816315	CGGCACCAGGGGCAC[C/T]GCACATCCTTCTGGC	220441
rs139198882	in-del	-/CCACTCA	0.0770498	0.180522	intron-variant	RNF152	GRCh38.p7	18:61861195	CCTAGGCCATCACAT[-/CCACTCA]CCACTCACATCCTGA	220441
rs139198900	snp	A/T	0.00597247	0.0543191	intron-variant	RNF152	GRCh38.p7	18:61817341	AGTTCTTTTTGTTTC[A/T]TTACTACTTAGGCTT	220441
rs139208842	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61843655	TGACACGTTACGACA[C/T]GGGTGAATTTTGAGG	220441
rs139219442	in-del	-/AG	0.06905	0.172502	intron-variant	RNF152	GRCh38.p7	18:61847152	TGCCACCAAGAAAAC[-/AG]AACTTTCAGAAATAA	220441
rs139229910	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61836359	TGTCCCCCCAAAATT[C/T]GTATGTTGAAACCCT	220441
rs139265034	snp	A/G	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61832161	CTAAACATATTAATC[A/G]ATAATAATCAACACT	220441
rs139265161	snp	C/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61872942	TTATTAGTTTATTTT[C/G]TTTCTGATAATAGCT	220441
rs139387092	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835683	CTGGATTCAATTCAA[A/C]AACAGAACCACATTC	220441
rs139398704	snp	A/G	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61821471	GAGGCTATGGAGTGA[A/G]GCTAATGATGGATCA	220441
rs139409842	snp	C/T	0.00993419	0.0697739	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810807	TGGTAAGAATTACCT[C/T]GTAGGTGACAATTTA	220441
rs139434772	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869534	AAGGAACACAAACTT[C/T]TGTGTTATTTCCATT	220441
rs139442509	snp	A/G	3.29506e-05	0.00405884	synonymous-codon	RNF152	GRCh38.p7	18:61815918	AAGCACGATGCCGAG[A/G]AGGAAGACCAAGACG	220441
rs139497201	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61878471	ATCCCAACAAACTCA[C/T]GTGTTAATCACTTGT	220441
rs139546526	snp	G/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61839934	ATTTCAGGCTCAACT[G/T]GTATTTCCCCATCCC	220441
rs139591556	snp	A/G	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61864996	TTGCACTCCAGCTTG[A/G]GCAACAAGAGGGAAA	220441
rs139599357	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61868934	CTTAAAATCAGATGG[A/G]CAATAAATTGCCTAT	220441
rs139655910	snp	C/T	0.0103295	0.0711199	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813755	AGGGCAAAGTCTATT[C/T]GAAATGTAGCATTCT	220441
rs139657840	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856995	AGCTATTACCCAGGG[C/T]AACATTTTAAATTAA	220441
rs139671026	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61868560	CTACAAAAATTAGCC[A/G]GGCGTCATGGCAGGC	220441
rs139744294	snp	C/T	0.0146672	0.084371	intron-variant	RNF152	GRCh38.p7	18:61880752	ATCAGGCAAAATGTT[C/T]TTAATTATGAAGCCA	220441
rs139764103	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812938	AGCCAGATAGAGATA[C/T]AGACAGACCTAGGAT	220441
rs139770706	snp	C/T	0.0146672	0.084371	intron-variant	RNF152	GRCh38.p7	18:61853541	AGGTGATCTGCCAGC[C/T]TTGGCCTCCCAAAGT	220441
rs139853960	snp	A/C	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61852664	GGAGAGATTTAAAAA[A/C]TTCCAGTGCTGTGGT	220441
rs139879390	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61845920	GGTGGGGCTTTGTGT[-/G]GGGGGGGCGTGGTGA	220441
rs139912839	snp	C/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61861219	ACTCACATCCTGAAT[C/T]ACTCAGAGCAACTTC	220441
rs139966146	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857344	ACACACTATGTCCAC[A/G]TGATTTTATTTTCAT	220441
rs139981918	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61837411	GTGTGATAATGGTGC[A/G]ATTATGTAAGAGAAT	220441
rs140003249	snp	C/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61817699	AAATCAAATATTCTA[C/T]AGTTAAAGGTTGACA	220441
rs140076634	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61836926	TGGATTACAGGCTTT[A/G]ACAGACAGGATATTT	220441
rs140133796	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61837812	ATATAATTTCTATTT[G/T]GCACAGACAAAGTGT	220441
rs140149548	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61850178	ACAAGCTGCTTGAAC[A/G]TGGGCAAGTTATCTA	220441
rs140149785	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889368	CTTAAGGTATTTATC[A/C]AATCTTTAAAATGGC	220441
rs140254976	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61844720	ACCATAGCACGGGTC[A/G]GTAGGTCATATGTGC	220441
rs140349016	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61836728	AATTTAAAAAAAAAA[-/A]TCCTTGACTCCATAG	220441
rs140369765	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891365	TCTTTGTTCTTGGAC[A/G]TGCATTTACATGGGC	220441
rs140388751	snp	A/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61866207	TTCTCCCTGCCTCTC[A/T]TCTCTCCCCAATACC	220441
rs140390769	snp	A/G	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61823253	GCATCCTGGTTTGCT[A/G]TATTTGATGAAGCAA	220441
rs140397049	snp	A/C/T	0.000560289	0.0167298	synonymous-codon	RNF152	GRCh38.p7	18:61816014	CTGCTCCTCCTCCAC[A/C/T]GCCTCCTGGGGAGCC	220441
rs140428147	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61827207	GCAGGCCACAAAGTA[A/G]CTGAATAAATTTCGA	220441
rs140442119	in-del	-/GA			intron-variant	RNF152	GRCh38.p7	18:61829526	ATATATCAGGGGAGG[-/GA]GAGAGAGAGAGAGAG	220441
rs140487902	snp	G/T	0.00914312	0.0669923	intron-variant	RNF152	GRCh38.p7	18:61826743	CTGATTCTCTTAAAT[G/T]TAGTATATTACTCTG	220441
rs140502965	snp	A/G	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61882678	CACATGTTAGTAATG[A/G]AGACTCAGAGAGAGA	220441
rs140510310	snp	A/G	0.0134861	0.0810011	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814879	AATACACAGAAGAGG[A/G]GCGAGTGTTGCAGGT	220441
rs140561178	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848022	TAACACCTTATGTAA[G/T]CTACCCATCTGATTT	220441
rs140573804	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841535	TTTCAGACATGAACC[C/T]ATACTGAGTCAAGGC	220441
rs140607697	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879197	TCCGAATGTGCACAG[A/T]CTTCTTCATTTTGTC	220441
rs140610804	snp	A/G	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61849392	TGGCTCCCTTTTCTA[A/G]AATTATGTCAAAAGT	220441
rs140668780	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61826307	AGAAACAAAGAGAAA[C/T]CCACCATAAATCCCC	220441
rs140707726	snp	G/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61850638	TCTTGGAAAAAGGAG[G/T]CTTTCAGTTTGGATC	220441
rs140728336	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811972	AACAGTTCCAAAGGG[C/G]AACAATGAATTTTTA	220441
rs140746940	snp	A/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61869866	AACTTGGCACAACAA[A/T]GATGTAAACAAAAAT	220441
rs140844137	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61827843	AGCTGCAGTAACTCA[A/G]TGAGGGTTGATTTTC	220441
rs140910064	snp	C/T	9.90426e-05	0.00703644	missense	RNF152	GRCh38.p7	18:61816135	CCGGGCAGCAGCGCA[C/T]GCTCCTTGGAGATGG	220441
rs140981445	snp	C/G	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61862447	GAGGCTTTCAAAAAG[C/G]TGGGAGGGAAGATTT	220441
rs140992566	snp	C/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61851323	ACTCTGCATAAACAC[C/T]GCATCTATACCATAT	220441
rs141016410	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829971	GTGTACAATTCAGTG[C/G]CTTTAAGTCACCATC	220441
rs141097305	snp	A/C/T	0.0115144	0.0749975	intron-variant	RNF152	GRCh38.p7	18:61833917	CCACAAGATAAAATA[A/C/T]CAGATGCGCTAAGAA	220441
rs141146590	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885182	TCTAATCTCATATTA[C/T]TAATCTTCGAGGAAG	220441
rs141184193	snp	C/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61828144	CCGCCACCCCGAAAG[C/G]TCCCCTTGTGCCTCA	220441
rs141191958	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61870230	AGCAGGGAGCTTTTG[A/G]TGGTCAAATCCAATT	220441
rs141253447	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880160	ACAAAACTCAGGTAA[C/T]AGCCAGAAATCTTGC	220441
rs141261815	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812378	CACAGGTTATACCAT[C/T]ACATGGTTTAACCTT	220441
rs141268201	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879651	AAGAAACAGTAACTA[A/G]AGAGGGAGGATTGTA	220441
rs141388364	snp	C/G/T	0.0170251	0.090679	intron-variant	RNF152	GRCh38.p7	18:61882158	TGTGGAATGCTCAAC[C/G/T]AGTAAATATAATGTT	220441
rs141428953	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61845977	TTAGTGCCCCTTATA[A/G]AATAAGTCCAAGGGA	220441
rs141429719	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61872410	AGAGCAACAGGCTAG[A/G]GACTAACAATGCTTG	220441
rs141557616	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61836172	TGGAGAAATGGTTGA[C/T]TCCAGGTCTGGGGCA	220441
rs141581532	snp	C/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61820502	AGCAATCAGGTGAGA[C/T]TATGATTGACTCTAC	220441
rs141622777	snp	A/G	0.0162398	0.0886349	intron-variant	RNF152	GRCh38.p7	18:61852397	CCAATCTGTGGTGCT[A/G]AACATACTCAAGAGT	220441
rs141635783	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854653	AGGTAGTGACTACAA[C/T]TTTCAGTTTTCTACT	220441
rs141649338	snp	A/C	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61860034	TGACTAGTGTCCTTT[A/C]ATACAGAAAAGACTC	220441
rs141666033	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863593	CCAGGCTGGAAAAGC[A/C]AAGGCTTCAGCTTTT	220441
rs141671728	snp	C/T	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61858077	GTCCTTCTGAAATCT[C/T]CCTCTGCAGCCACAT	220441
rs141750707	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61877579	ACACTTGAGGTTTTA[C/T]TACTTTCTACTGAAA	220441
rs141760515	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809568	TTTCACATGGGCTAC[C/T]AGCCCTACATCCCAT	220441
rs141787340	snp	C/G	0.00835141	0.0640778	intron-variant	RNF152	GRCh38.p7	18:61819854	AACGAGACTCTGTCT[C/G]TACTAAAAATAAAAA	220441
rs141865909	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839187	ACAGTCATTAAAATC[G/T]GGAAATCTACTTTGG	220441
rs141984385	in-del	-/TATA	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61827592	CCAGTGGGTTTTATA[-/TATA]GATATCTCTTTAAGT	220441
rs142047399	snp	A/G	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61842953	CAAGATGAGATTTGG[A/G]TGGGGACACAGAGCC	220441
rs142048666	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61838052	GACTTAAAGGCTTCC[C/T]GTCCCCACATACAAA	220441
rs142068414	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61873960	AAAGGAAAAGTAAAC[A/C]CCTTGCATCCTCTAA	220441
rs142088539	snp	A/G	0.0138799	0.0821421	intron-variant	RNF152	GRCh38.p7	18:61840611	CCTGGGTCCCAGGGA[A/G]CCTGAGAACTAGTCC	220441
rs142181095	snp	C/G	0.0792508	0.182605	upstream-variant-2KB, utr-variant-5-prime	RNF152, LOC105372159	GRCh38.p7	18:61894221	ATCGCCGGGTGGTCC[C/G]GGCGCGCCCGCTCCT	220441
rs142190304	in-del	-/TC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813257	CTGGGAGACTGAGAT[-/TC]TCTCTCTCTCTCTCT	220441
rs142193047	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61837633	TACAGATCTCCATTC[C/T]ACTTGCTCAGTTGTT	220441
rs142219268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890418	GCAGCATTTCCTTCC[C/T]GATGCTGCAATGATC	220441
rs142285250	snp	A/G	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61888764	TGGAGTCAGACTGCT[A/G]GATCACACAGTGTAA	220441
rs142300480	snp	C/T	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61864836	CCAGCCTGGCTAACA[C/T]GGTGAAACCCCGTTT	220441
rs142339845	snp	A/C/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61892364	TCACTGCATTTGACC[A/C/G]GTGCTCAATTAGAGC	220441
rs142396915	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61888253	CCACCCAAAGGAGAT[A/G]CAGGTCACAGATACA	220441
rs142406268	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61889188	AGCCGGGTGGTCTCA[A/G]CCTCCCTAGGTTGAT	220441
rs142412967	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61879007	AAAGAACAAATGGAA[A/G]GGAAAGTAAGTCTGC	220441
rs142416345	snp	C/T	0.0158469	0.0875917	intron-variant	RNF152	GRCh38.p7	18:61819298	ATGAGCTTAGTCAGG[C/T]ACAGGCCAGAGACTG	220441
rs142420867	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811546	TAAAAATACTACCTA[C/T]ATTTTAGTTTGGCAT	220441
rs142443462	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61860928	GGTAAAAGAAAAAAA[A/T]TAATTTTACAAATAA	220441
rs142454119	snp	A/G	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61822025	TACAGGAAGAGCAAG[A/G]TGTGATACTCCAATA	220441
rs142461115	snp	C/G	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61823524	GGCTGGTCTCGAACT[C/G]CTGACTTCAACTGAT	220441
rs142524854	snp	A/C/G/T	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812993	AAGTTCATATCCCCC[A/C/G/T]CTTTCTGCAGAATTA	220441
rs142585891	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876109	GTCTGGAAGACAGGA[A/G]CCACTTACCCCCATG	220441
rs142648764	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61870973	ATCAGACATCCCCGA[C/T]CCCATCCTGATAATG	220441
rs142714696	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849428	AGGTGGCCAATCCCT[A/G]AGCAATTACAACGAA	220441
rs142774871	snp	A/C	0.00953873	0.0683987	intron-variant	RNF152	GRCh38.p7	18:61887832	TCTGGATGTCTAGAT[A/C]AGAACTGAGCCGGGA	220441
rs142833641	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61872899	GCTCATTTTTGTAGT[A/G]AGCAAATAATTACTC	220441
rs142837580	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815443	TTTTTACACGGATTC[A/G]CAGGTTTAATTCTAC	220441
rs142856709	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61830530	GGCTTATTTCACTAA[A/G]CATGTCTTCAAGGTC	220441
rs142858315	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808946	GGACCCTCATGAGCT[A/G]AGCACATTACCCCAC	220441
rs142864696	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876929	AGCAGGATATTTACT[A/G]GAAAAAGAGACTTGA	220441
rs142898492	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812727	TTGGACACCAATGTT[C/T]TACAATTTTAAAAAT	220441
rs142918688	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857038	ACAAGGAGAAACCAG[A/C]ATTATTCAGTCAAAA	220441
rs142942188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845377	AGTGCCAGAACTCTC[A/G]CCAAGCCCACACATC	220441
rs142960702	in-del	-/A	0.0399052	0.1355	intron-variant	RNF152	GRCh38.p7	18:61871215	ACCTCCCCCCACCCC[-/A]AAAAAAAAACAGAAG	220441
rs143014366	snp	C/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61827893	GGAAAGAAAAAAGTA[C/T]AAACCTTGAAACTAG	220441
rs143065119	in-del	-/AAAC	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61877739	ATGCTGCACAAGAAA[-/AAAC]AAACAAAATCTGTCC	220441
rs143198276	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61864017	TGACTTCATCTTTCC[C/T]GCCCCTTACAGCCAC	220441
rs143236476	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853715	CTATTCTACCTCTTT[C/T]TCATAAAAACCCCTG	220441
rs143240883	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61867651	AACCCAGGGTGAACC[A/G]TATGTAAACCAGGCT	220441
rs143255842	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814491	ATAGGAATTTATCAC[A/G]TACTTGTAGCAGATC	220441
rs143298143	snp	A/C/T	0.00143493	0.0267474	synonymous-codon	RNF152	GRCh38.p7	18:61816245	GACAGCCAGGACCTC[A/C/T]GGGTCGTCCGGGAGC	220441
rs143373595	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865495	AAATTACTAATCCAT[A/G]TGACAAACCTGGTTG	220441
rs143414295	snp	G/T	0.0364509	0.129988	intron-variant	RNF152	GRCh38.p7	18:61871078	TAGAGGCTTTTACCT[G/T]AGGCTTCGATTCACA	220441
rs143415030	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61869239	CCTCAAATTTCAACT[A/G]CTAACTCCACAAAAT	220441
rs143663791	snp	A/C	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61851165	GTCTTACCTTTCTGA[A/C]CCATCAGAAACAGAC	220441
rs143668813	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61876662	CTGGCTTTTACTTGC[C/T]TTGTGACCTCAGGAA	220441
rs143679971	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851794	CCTCTACTTGGTCAA[C/T]ACCATAGGATACTAG	220441
rs143739862	snp	A/C	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61849328	ATTTTTGCTACCTTG[A/C]AGTTAACCCTGAGGA	220441
rs143793156	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61889601	TGGAAGCACAAATGT[C/T]CCTAAACTCTCTGGG	220441
rs143794849	snp	C/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61850428	AATTTCTTTGAGCAC[C/T]TGCTAGAATTATTCT	220441
rs143797765	snp	A/G	0.0115144	0.0749975	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61839000	AAGCTGAACTTGGCC[A/G]TCATCTTCTACAACT	220441
rs143835413	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61853090	GTCACATTTAACTAC[C/T]ACAAGAACTGGGATA	220441
rs143859398	snp	C/G	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61886688	TCTTGGGAAATGTGG[C/G]TTGATGACAAGACAT	220441
rs143863618	in-del	-/GGGAC	0.0119091	0.0762411	downstream-variant-500B	RNF152	GRCh38.p7	18:61807770	GTATATGGTTCACTT[-/GGGAC]GGGACCTGGGGCATG	220441
rs143864574	snp	C/T	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61855957	TCCACATACTTTAAT[C/T]TGACCACGCCATGTT	220441
rs143866165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864398	TTATGATAACAGATA[C/T]AACTCAGATCAGCCA	220441
rs143882510	snp	C/T	0.000494976	0.015724	missense	RNF152	GRCh38.p7	18:61816076	TGGTCACCACGGTGA[C/T]GGACTTCTGCTGGCT	220441
rs144041391	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835357	AGAAGTTTATGAATG[A/G]CTTTGGAATAGGAGC	220441
rs144054818	snp	G/T	0.00953873	0.0683987	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812597	GCTCTACTTAACATA[G/T]TAAGCATTCTCTTCC	220441
rs144093188	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61833389	GTGGAGGTAGCAAAG[A/C]CTCAAAGAATCCAAA	220441
rs144104747	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61828751	ATACTACTATTAATG[C/T]AGGCACATTCAAATG	220441
rs144114450	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836995	ATGATAAAGAGAGTT[A/G]TCTTTACAGATATCA	220441
rs144126658	snp	A/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61869586	CACACCTTCAATAAA[A/G]GATGTAGCAAAGTTT	220441
rs144135723	snp	A/G	0.0052649	0.0510366	missense	RNF152	GRCh38.p7	18:61816354	ATCTGCTGCAGGCAC[A/G]CTGAACAGCAGGTGT	220441
rs144167768	snp	A/C/G	0.000774453	0.0196631	missense	RNF152	GRCh38.p7	18:61816015	TGCTCCTCCTCCACC[A/C/G]CCTCCTGGGGAGCCC	220441
rs144258833	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841241	AAGTCACTACAAAGG[C/T]CTAAAATTCTGGACA	220441
rs144265767	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809003	TGAACTTGGTAGTCC[A/G]TACTGGAATGACAGA	220441
rs144331352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860327	TCATAAAACCCTCCC[A/G]ATTCAGAAGCAGCAC	220441
rs144355330	in-del	-/AGGAAGGG			intron-variant	RNF152	GRCh38.p7	18:61844156	ATTAAGAGAAAAGGA[-/AGGAAGGG]AGGAAGGGAGGAAGA	220441
rs144392780	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814177	TTCACATTAATTCCA[C/T]CACTTTTATATGCAT	220441
rs144399131	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881911	GTGTGGACTGCCTTG[A/G]GATGCAATTCTTAAA	220441
rs144413387	snp	A/C	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61885692	TCATAATAACACTCT[A/C]ATAATGATCAAGCAT	220441
rs144422930	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888964	AAAATATAGAAATGC[A/C]TTTTGGGGCTTCCCA	220441
rs144432502	snp	C/G	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61817437	GGATCCACTTAAGTA[C/G]GAATTTTTTGAATAG	220441
rs144481859	snp	A/C	0.0376037	0.131863	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810582	GAACCTGGGAGGCGG[A/C]GGTTGCAGTGAGCTG	220441
rs144607484	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61826365	GAAGACAGAAAGACC[A/T]CTCACACATGCAAAC	220441
rs144615980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859079	CACGACCCTGTATTA[C/T]AGACGAGGGCTGGTG	220441
rs144649901	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61840209	CCAGACACTGAATCT[A/G]CCAGCACCTTGATCT	220441
rs144670636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822098	ATGCATAAGAACAAG[C/T]ATATAAGAAAATATA	220441
rs144681444	snp	C/G	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61890218	GTCCCATAGGACACA[C/G]TTTCTAACCTCACCT	220441
rs144720420	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892739	GCCCTGTGCCAGCAC[C/T]GTCGGCCCAAATGAC	220441
rs144757927	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61868663	AGCCAAGATCACCCA[C/T]TGCACTCCTGCCTGG	220441
rs144768089	snp	C/T	0.0681886	0.171594	upstream-variant-2KB, nc-transcript-variant	RNF152, LOC105372159	GRCh38.p7	18:61894634	TCTCTCGCGCGCTCC[C/T]TCGGCTTTGCCCCCA	220441
rs144777307	snp	A/G/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61824391	GCTGGGTTTCCAACC[A/G/T]CATGGCAGTACTGCC	220441
rs144842887	snp	C/T	0.0146672	0.084371	intron-variant	RNF152	GRCh38.p7	18:61862849	GGCCCAGACTTATCA[C/T]TGGTGTGTGGGTAGG	220441
rs144879233	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61866321	ACGGGGACTCGTTTA[A/T]CCTCAGGACAACTTG	220441
rs144969087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879701	AGGCACGATGGCTCA[C/T]ACCTGTAATCCCAGC	220441
rs144972751	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810991	CACTCCTTTTGCACC[A/G]ATAACTTTTGAACTT	220441
rs144985165	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61862695	CATCGGTATCCTTTG[C/T]AATATCTTTTACAAT	220441
rs145004559	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822499	TGTGACAAAGTGCGC[A/G]CATTCATTTGGTAGG	220441
rs145008203	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842838	CAGATCTCAGGAAAC[A/C]CATTCACTATCACAA	220441
rs145008311	snp	A/C	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61882300	GTGTAAAAATAAAGG[A/C]AATTTATTAGATGCA	220441
rs145036836	in-del	-/AG	0.0146672	0.084371	intron-variant	RNF152	GRCh38.p7	18:61856750	GAAAAGTGGATTCAC[-/AG]AGCTGCTGACATCTC	220441
rs145088922	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874766	GCTAAGCATAGTGGG[G/T]TATCTAATCCCAGTC	220441
rs145139502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846551	CACAGATGCACATTC[A/G]TTGAGCACTTACTCC	220441
rs145167708	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61889976	TTCAGAGTAAACATG[C/T]ACTTGAAATAGGCAA	220441
rs145199973	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61853581	ACAGGCTGAGCCATC[A/G]CACCTCACCGGTTCC	220441
rs145218055	snp	C/T	0.0726307	0.176182	intron-variant	RNF152	GRCh38.p7	18:61863366	CTTGAACCTGGGAAG[C/T]GGAGGTTGCAGTGAG	220441
rs145262838	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61823460	ACCACCACACCCAGC[A/T]AATTTTTTTTGTATT	220441
rs145282102	snp	A/C	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61843978	TGTGTATTTTACCAC[A/C]GTAAAAATAAATAAA	220441
rs145346895	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61862105	TCCTAAGCTGGGGAA[A/G]GACCATGAGTGGGAA	220441
rs145356443	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850111	CCTAAGGCAATAATA[C/T]GGTAGTGTTGAAAAG	220441
rs145380156	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61821734	GGTGACAGACAATTA[C/T]CGCCTGAGCTCCACC	220441
rs145404380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858106	ATGCAAACCCTCTAC[C/T]CCAATTTCCAGGACC	220441
rs145444479	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61834624	CAATGACTGGCACTC[A/G]GTAAGTGCTCAATAA	220441
rs145511059	snp	A/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61827297	CAAGAAGGAACATTG[A/G]ATAAATTGCCCAAAC	220441
rs145529949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870155	CACCCACATTTATCA[C/T]GAATACCCTGCTTTT	220441
rs145539024	snp	A/G	0.0174175	0.0916809	intron-variant	RNF152	GRCh38.p7	18:61844916	GCCCCAGTGATTTAC[A/G]ATTTATAGAGGGCAA	220441
rs145549144	snp	A/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61827171	TTGGCCATAATTCCC[A/G]TGTTCCTTTGCATAG	220441
rs145596431	in-del	-/C	0.4087	0.193169	intron-variant	RNF152	GRCh38.p7	18:61831781	ACATGTTAATTACTT[-/C]TATTTTAAAAAGTGT	220441
rs145626608	snp	A/G	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61848157	CCTGATTTCAAAAGC[A/G]CCTCTGGGCTCCTCT	220441
rs145631289	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824772	TGTGCAGGAAGCCAA[C/G]GTTAGCGCTGGCATT	220441
rs145644970	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808767	ATACTCAAGTCAGGA[C/T]AGATCCACAGGAACA	220441
rs145711596	snp	C/T	0.0185938	0.0946107	intron-variant	RNF152	GRCh38.p7	18:61818259	GAAACCCTATCTCTA[C/T]AAAAAATACAAAAAC	220441
rs145819153	snp	C/T	0.0150606	0.0854603	intron-variant	RNF152	GRCh38.p7	18:61881657	TGATTATCACTGTCT[C/T]CCTAATTTATAAGGA	220441
rs145848903	snp	A/G	0.0126979	0.078662	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812176	GCCACTAGACACATA[A/G]GGCTATTTAAATTTA	220441
rs145860599	snp	G/T	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61887651	GTTACAGTGAGCTGA[G/T]ATCATGCCCCACTGC	220441
rs145924311	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61851849	TATACAGCAGTACAT[A/G]AATATAATAAACTTA	220441
rs145928342	in-del	-/ATATATAT			intron-variant	RNF152	GRCh38.p7	18:61829505	AGAGGGGAGAGAGAG[-/ATATATAT]ATATCAGGGGAGGGA	220441
rs145993270	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854735	CACTAGCACATCAGG[C/G]AGAAAAGAACCCAGT	220441
rs146054252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839355	CCTTGACTTTCATAA[C/T]GTTCACAGTTTTAAA	220441
rs146104794	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836708	AGACAGATGGTAATG[C/T]TTTATAAGACACTGA	220441
rs146104831	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876940	TACTGGAAAAAGAGA[C/T]TTGACCATTGTATCC	220441
rs146112787	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61885856	GCAACTACACCCAGT[C/T]ATCACAAATCCAGGC	220441
rs146125677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889362	CTTATGCTTAAGGTA[C/T]TTATCAAATCTTTAA	220441
rs146129614	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821169	TGCCCCAAGACCTGC[A/C/G]TACCATCATTGGTCA	220441
rs146177123	snp	C/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61820554	GGGAAGGATTGCTCA[C/T]GTTGAGCTACGGGTG	220441
rs146200073	in-del	-/AAAAG/AAAAGAAAAGAAAAG			intron-variant	RNF152	GRCh38.p7	18:61859880	CTCCACCTCAAAGAA[-/AAAAG/AAAAGAAAAGAAAAG]AAAAGAAAAGAAAAG	220441
rs146226156	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61860152	GGGAAGGGAGGAAGG[G/T]TTCTCCCCATGGGTC	220441

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