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
rs146233424	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61869423	TCTCCTGCACCTGAC[A/G]AGAGATTCTGTTACT	220441
rs146244727	snp	G/T	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61872931	AAAGATGTTTATTAT[G/T]AGTTTATTTTGTTTC	220441
rs146252723	snp	C/T	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61888831	CACCTTCTTCCTTTC[C/T]GGTTTCCATGACGTC	220441
rs146365876	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856719	TTGAGGGTCTGCAAA[C/G]TTAGGCACAGAAAAT	220441
rs146475727	snp	C/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61837335	ATGCCCAAAGTGATA[C/T]AAGGCATTTTAAAAT	220441
rs146521824	snp	A/T	3.3248e-05	0.00407712	missense	RNF152	GRCh38.p7	18:61816378	CAGGTGTGCTTGCAG[A/T]CCAGCAACTTGGGCC	220441
rs146532259	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61833804	CTTTCTGTCCATAGA[A/T]CTAGAATGGGGTGAT	220441
rs146603418	snp	C/T	0.00716266	0.059414	intron-variant	RNF152	GRCh38.p7	18:61817476	AGCCCTTTCTATGAG[C/T]GGGTTCTGCATCTGC	220441
rs146644709	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882045	TCAAATTCAAACATC[C/G/T]GAAATCCGAAATGCT	220441
rs146649781	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814225	GATAACAGACAGCAT[A/G]TAAATAAATTAAATT	220441
rs146718239	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61835388	CAGGTTATATTGTTA[C/T]GTGAAAGAGTTCACC	220441
rs146764844	snp	A/C/G	0.00518061	0.050666	intron-variant	RNF152	GRCh38.p7	18:61865525	GGCAGCACAAAAAAC[A/C/G]CAATACTATTTGTCC	220441
rs146799521	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61838584	TCCTCTGAAGTCCCC[A/G]GCAATCCTCCAACTT	220441
rs146835962	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811817	ATCATGCATAGCTTG[C/T]AAGTCAAACGTTTTA	220441
rs146836261	snp	C/G	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61853533	CTGACCTCAGGTGAT[C/G]TGCCAGCCTTGGCCT	220441
rs146886892	snp	C/T	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61850469	AATAATTCTTTTCTA[C/T]TCTTGAAAAGCAGAG	220441
rs146977797	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815490	TTTGTTTGAATCTAC[C/T]GCATTTAGAGAAGGT	220441
rs146979699	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61883861	TTTTTCCCCACTTCC[C/T]CCTGAGAAGGCCTAT	220441
rs146987713	snp	A/G	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61819320	CAGAGACTGTGGACC[A/G]TGGGCAGCCCCCAGT	220441
rs146989725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888401	CCTTTGATTTTTTGA[C/T]TTTACAATGGTGTGA	220441
rs146990589	in-del	-/C			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895793	GCATGAGCCACCGCG[-/C]CTTTTTTTTTTTTTT	220441
rs147074086	in-del	-/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895510	TTTTTCTGTTTTTTT[-/T]TTTTTTGAAGATGGA	220441
rs147083722	snp	A/C	0.00953873	0.0683987	intron-variant	RNF152	GRCh38.p7	18:61867657	GGGTGAACCGTATGT[A/C]AACCAGGCTGAACTC	220441
rs147093645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870363	TCTTCATGTCTGATG[C/T]ATTTCCTGTCCTCAT	220441
rs147131478	snp	A/G	0.0150606	0.0854603	intron-variant	RNF152	GRCh38.p7	18:61881017	CTCTGGGGTTCAAGC[A/G]ATTCTCCCATCTCAG	220441
rs147141178	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61844518	CACTGGCTCTGGTGG[A/G]TTTTATGTGCTTGTT	220441
rs147236157	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864680	GTTGGTTCCTCTGGC[A/G]ACCAGCTGGCACTCT	220441
rs147336502	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61829700	GGTCCAAACCTTTCC[C/T]CTCCTCTTCCAATCC	220441
rs147354521	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878347	AAGAATTATCCAGCC[C/T]CAGAGGTCAAAATGC	220441
rs147358382	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810792	CAATAGTTTCTGTTT[C/T]GGTAAGAATTACCTT	220441
rs147441393	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812927	GAAAGGATCATAGCC[A/G]GATAGAGATATAGAC	220441
rs147443272	snp	C/T	0.0189856	0.0955633	intron-variant	RNF152	GRCh38.p7	18:61880185	TCTTGCTGCAAATTT[C/T]CCAACAAAACTTGAC	220441
rs147542758	snp	A/G	9.89952e-05	0.00703476	synonymous-codon	RNF152	GRCh38.p7	18:61816251	CAGGACCTCCGGGTC[A/G]TCCGGGAGCTGCGAC	220441
rs147547933	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864056	TCTACCCATAGAACA[C/T]TTCTGACATCAAACA	220441
rs147553692	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840531	TTCTATCTGATTGCA[A/T]CATCCTTGCCATACT	220441
rs147595753	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837854	CCTGGCTCACAGCAG[C/G]CAAATGCATTCTTTC	220441
rs147658470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821825	CACATGCAAGGGATC[C/T]AGACTGCACACTCTT	220441
rs147690691	snp	C/T	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61858415	CTTCCCTCCCCCAAG[C/T]TCTCTGGACCTATCT	220441
rs147700225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862330	TCCCATTTCACACAC[A/G]AGGAAACTAAGGCTC	220441
rs147868003	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857795	TTTCAGCCTCAGTCC[C/T]GTTAATCAATAGTCA	220441
rs147901346	snp	A/C	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61890404	TAGAGCAAGACCCTG[A/C]AGCATTTCCTTCCCG	220441
rs147911575	snp	C/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61854021	GTTGACTTGCCCAGG[C/T]CCACACCTGGAAATG	220441
rs147932811	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841350	TTATTAAGGCACAAG[C/G]AACCAATATTCATGA	220441
rs148012807	snp	C/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61889096	ATGGTCTATATCTGG[C/T]TCTTCCTGCTGGTCT	220441
rs148017467	snp	A/G	0.0197687	0.0974348	intron-variant	RNF152	GRCh38.p7	18:61863429	ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA	220441
rs148022016	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61848963	ACAAACCAATAGCCC[A/G]TGGAGATCCTGGACT	220441
rs148025950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819560	ATCTTGCAGGGTATT[A/G]CAATGAGGTTGTACA	220441
rs148069344	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61858906	GCCTGAGACAAAACA[A/G]AAACTAAATTTGGGG	220441
rs148183342	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61884718	GTGCCCACCACCATG[C/T]CTGCCTAATTTGTAT	220441
rs148228697	snp	C/T	0.0205511	0.0992634	intron-variant	RNF152	GRCh38.p7	18:61828138	ATATTTCCGCCACCC[C/T]GAAAGGTCCCCTTGT	220441
rs148235456	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880038	TCCTAAGCTCCCAGA[C/T]TCTGACAGAATCTCT	220441
rs148282629	snp	G/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61890741	ACACTACCTTGAAAA[G/T]CAGAGGGTGCTGACA	220441
rs148323240	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809325	TAAGGTACCAGCTAC[C/T]GTGTTCTCCCACTAT	220441
rs148376059	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871740	GTTCTGGTAGGGACA[A/T]CTCATGGCCCACCTT	220441
rs148391715	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852100	CACCCAGGAATATGA[C/T]GAGGCCAGCAGCAAT	220441
rs148398108	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61834423	AGAATGATCATATTT[-/T]GTGTCCTTTTAGTCT	220441
rs148513320	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61849486	CACCTCTTTCCCCCA[A/C]CAGCCACACGAAGGG	220441
rs148538384	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61830416	CAGCCCCTGCTAACC[A/G]GTCACCTTTCTGGCA	220441
rs148591629	snp	A/G	0.0111196	0.0737302	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895011	GGACAAGAAGCAGGG[A/G]AGTAAAGAGATGCAA	220441
rs148598928	snp	A/G	0.00212613	0.0325353	synonymous-codon	RNF152	GRCh38.p7	18:61816164	GGGCAGGGGCAGCAT[A/G]TAGCACCCATTGCTG	220441
rs148634020	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61878942	ACTTACACTAGAGCT[A/G]GAGAGGCAACCATAT	220441
rs148637652	snp	A/G	0.000165046	0.00908273	synonymous-codon	RNF152	GRCh38.p7	18:61816278	CGACACGGAGAAGCC[A/G]GGAGGCAGCTTGGTG	220441
rs148686076	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61873620	ATTACAGGCATGAGC[C/T]ACCACGCCCAGCCTC	220441
rs148749523	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61864770	AAGGAGTTTATGGTC[A/G]GGCACAGTGCTCACG	220441
rs148758144	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821416	CTGGAGCGTAATTAG[C/T]AATGATGATGATTCG	220441
rs148802224	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61860405	CAATAACAGATCACA[C/T]AGAAGATGCTGGTCC	220441
rs148845355	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61844918	CCCAGTGATTTACGA[C/T]TTATAGAGGGCAACT	220441
rs148850550	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834641	TAAGTGCTCAATAAA[G/T]GCTTGTAGAAGGGGT	220441
rs148888456	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858855	AAAAACAGAGATCCC[A/G]TTTTAATAGGAGATG	220441
rs148918814	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818791	TCATTTATTCATTCA[A/T]ATTTTCATTGCATAT	220441
rs148964462	in-del	-/GACA	0.0437281	0.141251	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810874	ATCTAAGTCAGGGAT[-/GACA]GACTGACTACCTGAC	220441
rs148998448	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876524	GTTAGTCGAAGTCAT[G/T]AAAATACAGGAGATC	220441
rs149053440	snp	A/G	0.00914312	0.0669923	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811256	ATGGGAACTCTTAAA[A/G]TCAAAATCTAGACTG	220441
rs149060828	snp	A/C	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61866422	AAGCTACAGAGTGAG[A/C]ATCTGCGAGGACAAG	220441
rs149112374	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862782	TCATCAAAGCCAAAG[C/T]GGGGGTTCTGGGGAC	220441
rs149208678	snp	A/C	0.0667028	0.170006	intron-variant	RNF152	GRCh38.p7	18:61842749	GAAGGCAAGGAGGAG[A/C]AAGTCACATCTTATG	220441
rs149213369	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814390	GGAGTCCTTGTCACA[C/T]ACCACTTGCTTCATG	220441
rs149253156	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61888904	CTCTACCTGACCAGC[C/T]GACTTGGGTATGAAA	220441
rs149274529	in-del	-/A	0.0919752	0.193722	intron-variant	RNF152	GRCh38.p7	18:61859011	ATATCCAATTACAGG[-/A]GGGTGAAGGAGGCCC	220441
rs149348247	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61868608	CTCAGGAGTCTGAGG[C/T]AGGAGAATCTCATGA	220441
rs149358437	snp	A/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61830147	CTGCCTCAGACTCCC[A/G]GGTAGCTGGGACTAC	220441
rs149369104	snp	C/T	0.021333	0.101051	intron-variant	RNF152	GRCh38.p7	18:61879833	AGCCAGGTGTGGTGG[C/T]GCACGCCTGTAACCC	220441
rs149373068	snp	C/G	0.00953873	0.0683987	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812593	CTTGGCTCTACTTAA[C/G]ATATTAAGCATTCTC	220441
rs149411236	snp	A/G	0.0115144	0.0749975	intron-variant	RNF152	GRCh38.p7	18:61824141	TCAGTATTGCAGTGA[A/G]TGATGATAACTACTG	220441
rs149431859	snp	C/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61838706	GATGGCACTAGAGGG[C/T]CAACAAAGATTGATG	220441
rs149464964	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855916	GAGTAAACTGAAAGA[C/G]AGTACACCTGCTAAG	220441
rs149579288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848504	TAGCAAGCAACATCC[A/G]TAAACTTACTACACA	220441
rs149591721	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61836700	GCTAGCTAAGACAGA[C/T]GGTAATGTTTTATAA	220441
rs149618143	snp	A/C/T	0.000346575	0.0131601	synonymous-codon	RNF152	GRCh38.p7	18:61816263	GTCGTCCGGGAGCTG[A/C/T]GACACGGAGAAGCCG	220441
rs149622141	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61860284	GCCCTAGAAAACTCA[C/T]CTAAGGGGGAAGCAA	220441
rs149660042	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61870090	TTATTCCAAACCTCA[C/T]GCTCTCTTGGAAAGA	220441
rs149680918	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61881262	GCTTGGGGAAAACAA[A/G]ATGTATTTAGCTGTT	220441
rs149688390	in-del	-/T	0.464947	0.127663	intron-variant	RNF152	GRCh38.p7	18:61831922	ATAGTATTATGTGTG[-/T]GGGGGGGTGTGGGTG	220441
rs149716744	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61840048	AGGTGGGCTCACTGC[C/T]ATTGGGTATCACTGC	220441
rs149844349	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818086	AGAAAGCACTCCCCC[A/G]TCATGATATATAATG	220441
rs149875511	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810980	CTTTTGTGTATCACT[C/T]CTTTTGCACCGATAA	220441
rs149892028	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61849912	TTCTGGGTAAGTTCT[A/G]TCAAGTACTGTGTGA	220441
rs149929258	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61873441	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	220441
rs149935114	snp	C/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61862633	CACCCACGGAGGGCA[C/T]AGAAGCTCCACACCC	220441
rs149987502	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61889974	ACTTCAGAGTAAACA[C/T]GCACTTGAAATAGGC	220441
rs150010474	in-del	-/T	0.0704125	0.17392	intron-variant	RNF152	GRCh38.p7	18:61828432	CTTTTCCAAAAAACA[-/T]TTTTTTTGTAGAGAC	220441
rs150091344	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834354	CCAAGAAGCTTTCCC[A/G]TTCCCCTCCAGCTGG	220441
rs150192990	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812499	ACTGGAACCAAAAAC[C/T]AAGTTGCCTTTTCAT	220441
rs150208668	snp	G/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61851425	CTTACCCAAGCGCCT[G/T]AGCTGCCCCAGCTTC	220441
rs150239694	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876265	ATTCCTATACCACCT[A/G]GCAATTGCATCCCTT	220441
rs150244400	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807788	GACCTGGGGCATGCA[A/G]CACAATTTCTAAACA	220441
rs150251340	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863685	TCCTCAACTAGCATG[C/T]TGTACAAAGTGCGTT	220441
rs150297373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61892091	ACATCAAAACAGAAC[C/T]ATCCTTGGAAAGAAA	220441
rs150386212	snp	A/G	0.00597247	0.0543191	intron-variant	RNF152	GRCh38.p7	18:61855649	GCTGCAGCCCCTGGT[A/G]TGCCTGGCTGTGCAC	220441
rs150412069	in-del	-/ATATAT			intron-variant	RNF152	GRCh38.p7	18:61829505	AGAGGGGAGAGAGAG[-/ATATAT]ATATATCAGGGGAGG	220441
rs150439691	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61883154	TCAGCCCCTCAACCT[C/G]TCCTGGAATGCATGT	220441
rs150455762	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841734	GCCTCTCCATGAAAC[C/T]GCAAGTGAAGAACTG	220441
rs150472485	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879227	CATTACTTGCTAAAC[A/G]ATACAGTATAACAAC	220441
rs150505350	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813036	ATCTACAAAATGAAG[A/C]CACCGGAGGCTGCTT	220441
rs150525680	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61823862	GCTGCAGCCTAGGTG[C/T]TGTCCCTGTCTGGAT	220441
rs150541292	snp	A/G/T	0.000395351	0.0140543	synonymous-codon	RNF152	GRCh38.p7	18:61815915	GTGAAGCACGATGCC[A/G/T]AGGAGGAAGACCAAG	220441
rs150552851	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877646	CAAAATTATTAGGGT[G/T]GTAGGAATAACAAAT	220441
rs150556674	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810202	TCCAATATTGTATAA[C/T]TCACAAATTGGAAAA	220441
rs150615882	snp	A/G	0.0592355	0.161582	intron-variant	RNF152	GRCh38.p7	18:61868519	ACCAGCCTGGCCAAC[A/G]TGGTAAAATCCCGTC	220441
rs150715430	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61849813	CTCAAACCATCCTCC[C/T]GCCTCAGCCTCCCAA	220441
rs150767155	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61843651	ATTCTGACACGTTAC[A/G]ACATGGGTGAATTTT	220441
rs150820859	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872447	AATCTTACTATCAGA[A/G]CCAAAACTATTGCTA	220441
rs150883084	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828266	TCTTTTTTAAGAGAC[A/G]GGGTCTTGCTATGTT	220441
rs150912190	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61889723	TAAACACATTCCTGC[C/G]CCCTTCAGATCTTAT	220441
rs150916988	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821456	GAGAAGGAAATTTAT[G/T]AGGCTATGGAGTGAA	220441
rs150986057	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61864845	CTAACATGGTGAAAC[C/T]CCGTTTCTACTAAAA	220441
rs151029357	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61851245	TTTTAAATCAAACTT[C/T]ATTTTTTATTTTCAT	220441
rs151040901	in-del	-/A	0.0596104	0.162024	intron-variant	RNF152	GRCh38.p7	18:61875581	ATTACCCACGAAGGT[-/A]CAGCTCTGACCTGTC	220441
rs151072439	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61887937	CACAGAACACAGCAT[C/T]TGGAGATTCTACTTC	220441
rs151081890	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61845437	ACCACTCAGGCCGCC[A/G]CTGCTCAAACTGACT	220441
rs151093347	in-del	-/A	0.0256215	0.110247	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813322	CACACACACATACAC[-/A]AGAATGCACACCCCA	220441
rs151135433	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61874344	CCAACATATTGTATT[C/T]CCGATTACAGATACA	220441
rs151145615	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61837811	GATATAATTTCTATT[A/T]TGCACAGACAAAGTG	220441
rs151197186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830601	TGAGTAATATTCAAT[C/T]GTGTATTATTTTTTC	220441
rs151235340	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61882517	TGAGGTTACAGAACT[A/G]GCAACCAACAAACTA	220441
rs151286121	snp	G/T	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61826511	TTTCCCCTACTAAGT[G/T]AGGTATGTAATCCTT	220441
rs180738425	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61821889	GTGGAACAGTTTCAT[C/T]CTGAAACCATCGGTC	220441
rs180751777	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813865	GCAGCCTGGGAGAGT[C/T]TGAGAAATTGACACT	220441
rs180779039	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61853958	CCCTGCCCACCTGCC[A/C]ATTTTTCAACTGAGA	220441
rs180784842	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61883275	TGTCTACTGTGTACC[A/G]GGCCCCAAGCGGCTA	220441
rs180799030	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842180	ACCAGCAATTCTGCT[C/T]ATGACATTTTTTCCT	220441
rs180816122	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864286	CAGTGGGGTTTCTCA[A/C/T]AACCCCCTCTCCGGT	220441
rs180955299	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61874542	AGTAAGAGACATAAC[A/G]GTTCTCATGGTTACT	220441
rs181052790	snp	G/T	0.040671	0.13668	intron-variant	RNF152	GRCh38.p7	18:61884228	GTTCTCCCCCATTTT[G/T]CAGCTGAAGAACAAA	220441
rs181056355	snp	C/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61865316	AATGTAAGGTTTCTT[C/G]TTCAGATTTAAATGT	220441
rs181062968	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842437	CATTGCTGGAACAAG[G/T]CTGGCAGCTGTCACA	220441
rs181146022	snp	C/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61822355	TGTGTTGTTGTTGCT[C/G]TTGTTATTTTGAGGC	220441
rs181220302	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812772	TTGATAGTTGTCTTT[C/T]AACATCTATACTCAT	220441
rs181286250	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818148	AACCAACCTGGCCGG[C/T]GTGGGGGCTCACACC	220441
rs181354640	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61868855	ATGTAGTCAAGTCAG[A/G]AGCAGGCATTACAAA	220441
rs181357766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826135	CACTGGAAACCCCAG[A/G]GTTGGTATAAAGACT	220441
rs181360480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847082	CTGCTCAGCAAACAC[C/T]GGTACTCCTCCCCCA	220441
rs181389074	snp	C/T	0.0134861	0.0810011	intron-variant	RNF152	GRCh38.p7	18:61837308	AATGAGATCCAGGAT[C/T]GAGTGGGGAAAATGC	220441
rs181441460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860120	ATGCCAAGGACTGCC[A/G]ACAGCACGAGAAGCT	220441
rs181526029	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808484	TAATAGCCTCTGAGC[A/T]GCATTAATATAGCCA	220441
rs181570684	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61878575	GTTTGTGCTGCTACA[A/G]CAAAATACTTGTGAT	220441
rs181603910	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880475	AAACTCGCCACGTAA[A/C]CTTGGACAAGTCACC	220441
rs181612929	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61860667	TTTATCAGTATTTTA[C/G]AGTGTACTCCTACTT	220441
rs181654825	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61847806	GTCAATGGCCTGGCC[G/T]TCACACCTACTCTTC	220441
rs181736038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869638	CCAGGAGGGTGCCAG[A/G]AAGACACCACAGATC	220441
rs181798589	snp	A/C	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61848744	GAGCCACGGAAGAGG[A/C]CTGCCCGGCAGGAGC	220441
rs181801778	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877995	TTAGGAACCCAGGTT[A/C]TTTCTGCCATATCCT	220441
rs181810814	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859517	AGCTGCAGAGAAAAG[A/G]AGCATCACCCACCTG	220441
rs181814397	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61888875	CCAGAAACCACTTTC[A/G]TGCCACAAGAGTCCT	220441
rs181884551	snp	A/C	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809146	ATTAAGTATTTTCTC[A/C]CTCTTTGGGTATATC	220441
rs181892113	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61828223	TGCTTTTCAGAGAAT[C/T]TGAGTTTGCGTTTTT	220441
rs181928005	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61831309	ATTACAGAATCAGCT[C/T]GGGGAAATGCTCGGA	220441
rs181937498	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61869897	GAGAAAGTTTATAAG[A/C]AGATGTACTTTGGAC	220441
rs182003502	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885224	CCTACCCCAGAACAA[C/T]ACAACTGCAAAAGAA	220441
rs182033323	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836860	ACCATTTTACCATCT[C/T]CAATGTAATGACCAA	220441
rs182077958	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852810	AACATAAGGCACACA[A/C]CTGCCTGCTCCCCTA	220441
rs182092226	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813354	CAAACAGGTACACAA[A/G]TAACTGCAAGCAGAT	220441
rs182150235	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822597	TATGAGCCCAAGGAT[A/T]AAAAAAGCCAGTGAA	220441
rs182246934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876620	CATCAATGCTGGAGA[C/T]GTCTTGACTGGGTTC	220441
rs182255642	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856115	ATGACCTTCCAAGTT[C/G]TTTTCCAATTCTGAC	220441
rs182300857	snp	C/T	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61865720	GAATTTTCTGAACAT[C/T]AGAGTTTAGACATAG	220441
rs182302794	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896364	CAAGTAGCTGGGAGA[C/T]TTCAGGAGTGCCACC	220441
rs182315386	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61816994	AAGTAAATTTCTCTC[C/T]TTAGATCCTCTGACC	220441
rs182384767	snp	C/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61823071	TGTCATTGACTTTTT[C/G]TCCTCTGGTAGCAAA	220441
rs182495739	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61866338	CTCAGGACAACTTGA[A/G]GAAGTCACCCTCATT	220441
rs182568903	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61842775	TTATGTGGACAGCAG[C/T]AGGCAAAGGGAGAGC	220441
rs182582830	snp	C/T	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61874241	GCCGCAGTTTAACAG[C/T]GCATGAACTGACCAA	220441
rs182642341	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885765	CCAAAATCAAAAAAA[C/G]GGAGGTAAAACAGAT	220441
rs182659222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843558	AAAATACCCAAATGC[C/T]CACAGACAGATGAAT	220441
rs182666426	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61823546	TCAACTGATCTGCCC[A/G/T]TCTCAGCCTCTCAAA	220441
rs182670000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886817	TAGGTGATAATACAA[A/G]ACAATCTATGACAAG	220441
rs182685095	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815491	TTGTTTGAATCTACC[A/G]CATTTAGAGAAGGTC	220441
rs182709630	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61828430	CTACTTTTCCAAAAA[A/T]CATTTTTTTGTAGAG	220441
rs182719584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820441	CAAAATACAGGGTTC[A/G]TTGGTGAATCCTGCT	220441
rs182786228	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818884	ATAAGAAAGTCCTGG[A/C]CTAGAGATGGGAGCG	220441
rs182792101	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875033	GATATGCCATGGTCT[C/G]CAAGATGTTGGAGGC	220441
rs182794202	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61839130	CAGGCCTGAGGTCCC[A/G]TTATCCCCATATGCT	220441
rs182803602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890069	CAACATATTAGTAGT[A/G]CATTACAGGTGGGGG	220441
rs182808294	snp	C/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61870992	ATCCTGATAATGGCA[C/G]CCCAAGGCCCTGCAC	220441
rs182813106	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849178	GGAGTACTGCCCTGC[A/G]GGGGCTTCACCAGCT	220441
rs182929948	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866063	TCTTATGTCTGCGTG[C/G]AGGAACAGGCAGGAA	220441
rs182963191	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61832736	GAGTCTTCTGGGCCA[A/G]CAAATAAAATCGACA	220441
rs182974443	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833844	AAGGTGACCTCTCTC[A/T]ATTATAGCTACTTTC	220441
rs183066318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881202	TAGGTGTGATCCACC[A/G]CACCCGGCCTTCTCT	220441
rs183086839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854855	AACCTGACGTGAAAA[C/T]AGCAGGCGGAAAAAA	220441
rs183133057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862684	ACGTGTCTCTTCATC[A/G]GTATCCTTTGCAATA	220441
rs183228411	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872374	TGAAGTTCCTTCCAG[C/T]CCTAGAGGTGGAAAC	220441
rs183232006	snp	G/T	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814256	GTCTTGACCTCACAG[G/T]GCTATTTTCTAGCCT	220441
rs183234853	snp	C/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61850571	AGTTACTGAGAGGCA[C/G]ACTCAAGCTCCATAT	220441
rs183277288	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815074	TACACAATATTTACA[A/T]TTGAAATTCTTATTT	220441
rs183281545	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833333	GTTATTGAGTAACTT[A/C]AAATAAAACAAGGTC	220441
rs183297864	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809839	TATATAGTGGGATAC[C/T]CCAGGCAGTGAATCC	220441
rs183390956	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61881535	CACCTTTACTAAAAG[C/T]GGTAACAGAAGCTAA	220441
rs183402481	snp	A/G	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61876184	CTGTCTACCCTTCAC[A/G]GGCATTGTCAAATAC	220441
rs183408843	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840273	AGTTTCTGTTGTTTA[A/T]AAGCCACCCAGTCTA	220441
rs183411350	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855755	TCTGGGCTGGTAGCA[C/T]GAACTGAGCGCAGCT	220441
rs183491765	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61892383	CTCAATTAGAGCACT[A/G]GGCAAAAGTACAATC	220441
rs183532767	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB, nc-transcript-variant	RNF152, LOC105372159	GRCh38.p7	18:61894593	CCGAATCGCCCACCT[C/G]CCCCGGGGTGAGGGG	220441
rs183657488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839661	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	220441
rs183659530	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61844996	GGCCATAAGTGGACA[C/T]GAGTGCTGAAAACAT	220441
rs183739085	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61871735	GGCTTGTTCTGGTAG[G/T]GACAACTCATGGCCC	220441
rs183746992	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61825711	CTCCAAGTAGCCAGG[C/T]TCCCTTGGAGAGCAA	220441
rs183780932	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61828621	CCCAATCCATAGGTA[C/T]TGGTTTAGAAAAAAA	220441
rs183788477	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61878082	ACGAGGGTAGAAAAG[A/G]CATCCCACTCTGAAC	220441
rs183817717	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61826222	ATCCCTTACCTGACC[A/G]AAAGCAGAAACTTCT	220441
rs183868792	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862300	TGTGGCAGAGGAGGC[A/G]GCAAAAATTCTCATT	220441
rs183945949	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61888616	GACAAGGCTGAGCTA[C/T]GATGTCAGTAGGTGT	220441
rs183950668	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61868957	TTGCCTATACTTGAG[A/G]TTCTTAGGGTTCCCA	220441
rs183963495	snp	C/T	0.00372053	0.04297	intron-variant	RNF152	GRCh38.p7	18:61847151	TTGCCACCAAGAAAA[C/T]AGAACTTTCAGAAAT	220441
rs184022051	snp	A/T	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61820180	TAAAAATACAAAAAA[A/T]TAGCCAGGCATGGTG	220441
rs184027596	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893543	TCCAGCTGGCTTTGT[C/T]CTGCCGCTGTCCTTC	220441
rs184070318	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822081	AAGAGTACTTCAGTA[A/G]AATGCATAAGAACAA	220441
rs184081391	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61842303	AGCCCCTTTGTGGCC[A/T]AGTTTTCTAACTCAC	220441
rs184089917	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61873399	CTGGGGTGCAATGGC[A/G]CTATCTCGGCTCACC	220441
rs184099636	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61850765	TGGTTTATCCAAACC[A/G]CTTGTTTGAGCTCAG	220441
rs184108799	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61885499	TTTTAGTAGAGATGG[C/G]ATTTCACCATGTTGG	220441
rs184204402	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61864891	CAGGCGTGGTGGCGC[A/G]TGCCTGTAATCCCAG	220441
rs184343857	snp	C/T	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61884078	AACTGAGCCCAATGA[C/T]TGGTGGATGGTAGAT	220441
rs184385080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887742	CTCCCTATTTCTACA[A/G]TATCTGTCAAAGCTT	220441
rs184433052	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61877757	CAAACAAAATCTGTC[A/C]CTTTTTTTGTGTTTG	220441
rs184517996	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61868364	ACCCAGCCCAGCCAC[A/C]CCCAGCTGATCCTGC	220441
rs184555906	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834378	CAGCTGGCTTAGACA[C/T]CACTTCTATGTTCTC	220441
rs184579269	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882113	CAAAGGAAATTCTCA[C/T]TGGAGAATTTTGGAT	220441
rs184583198	snp	C/T	0.00716266	0.059414	intron-variant	RNF152	GRCh38.p7	18:61863313	GGTGACACACGCCTG[C/T]AGTCCCAGCTACTCG	220441
rs184593774	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840962	CCCAGCTTCCATCTC[C/T]AGAAGCACCTGTCCA	220441
rs184657292	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61820715	GACATCATATCAAAA[C/T]AGTGACCACCGATTT	220441
rs184695486	snp	A/C	0.00398564	0.0444627	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810733	TTAAATAGACTACTA[A/C]TTTCAAAACAGCTAC	220441
rs184732941	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877197	ATGAAACCATTTGAC[C/T]TACGTATTTTGGTCA	220441
rs184869981	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61857630	TCGCCATGTTCTGAC[A/G]ATACAGGGACACAAA	220441
rs184947132	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812285	GTGCCTGGTGGCTAC[C/T]GTACCAGACGGCACA	220441
rs184987250	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61816751	ACAGGATTCCCATAA[C/T]GCCCAGTGAAAGGCG	220441
rs184997985	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61835273	CTAAATTCCTATCCA[C/T]AGGAATCTGACTAGA	220441
rs185017682	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859298	GTTGACTGAAGTGAA[A/G]CAGGCAACAGAGCGT	220441
rs185186352	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61874742	TTAATTTAACTACTT[G/T]GGTTTAGGGCTAAGC	220441
rs185194523	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895898	CACAATGTACTGAGA[G/T]CACTCTTGTCATGTC	220441
rs185208592	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61851961	GGCTCATTAAAATAA[C/T]TTTATCTATAATATC	220441
rs185305976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61818523	AATGAAAAGATCAAC[A/G]TACTTTAAAATACAT	220441
rs185314002	snp	G/T	0.0023933	0.0345097	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813016	CAGAATTACAAAACG[G/T]ACTCATCTACAAAAT	220441
rs185314276	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61873830	AGTGGACTTGTTTTC[C/T]GAGAAAATGGAACAG	220441
rs185315234	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870094	TCCAAACCTCACGCT[C/G]TCTTGGAAAGAAATA	220441
rs185321554	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61848885	GGGCAAGAGAGCCAG[C/G]ACACAGCCCACAGAG	220441
rs185442317	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830865	GTGAAGAGAGTGGCA[A/T]CTGAAGGTTAGAGAT	220441
rs185484246	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809170	GTATATCTGCCTGTC[C/G]CTTCACATAGACCCA	220441
rs185490538	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828356	TCCTTGCCTCAAGCA[A/T]TCTTCCTGCCTTAGC	220441
rs185499459	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61821325	GCCTTACAAGCCATT[C/T]TGACAGCAGCCTCTC	220441
rs185520154	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882536	ACCAACAAACTAATC[A/C]CTGTTGCTGGCAATT	220441
rs185538387	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841587	TCTTAACTTTGGGGG[A/G]TTACAAGTCATTCTG	220441
rs185614731	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61825116	CAGCTACAAAGAACA[C/T]AGCAGTGAGTAAGCA	220441
rs185621955	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891617	TTTGCAAAGCACTGG[C/T]CTTTGTTTCACCTGG	220441
rs185661411	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61863834	AAGTCAGAGCCAGGG[C/T]GGAGTGGCAGGTGTC	220441
rs185671892	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61867852	GCCACGAATGTCCAG[C/T]GCACACTAATTCTAT	220441
rs185725653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880490	CCTTGGACAAGTCAC[C/T]AGGCTTTTCCAAGTT	220441
rs185734508	snp	A/C	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61861757	CTGGCATGTGCAGAG[A/C]TCACATGGTGAGAGA	220441
rs185784586	snp	A/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61819032	GGCTATTTTCAGGTT[A/T]TGGAATCAGCATGAG	220441
rs185794721	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61887447	CTCCTGGCTAGGTGC[A/G]GTGGCTCACGCCTGT	220441
rs185795454	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839339	AAAGTCCCTAGTCTT[C/T]CCTTGACTTTCATAA	220441
rs185868249	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61831943	GGTGTGGGTGTGTAT[A/G]GGGGTGTGTGTCTTG	220441
rs185881107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865397	TTCATTAATAACTAC[A/G]GCTTGAGAATTTGAA	220441
rs185889032	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61842561	CCTTCATGGCAAAAA[A/G]TCAAATGCTTGACTA	220441
rs185961480	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61854101	CCACTGCTTATTGAC[C/T]CCCCGTGACAAGGTG	220441
rs185981269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859610	TAGGCCGGGCACGGT[A/G]GCTCATGCCTGCAAT	220441
rs185989058	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813915	TTATGTAATAGAGGA[C/T]AGTATTCAGCTAATA	220441
rs186032055	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61822394	TTTTGTGCTTTTGAA[A/G]GTCCTTTACAATAAC	220441
rs186048444	snp	C/T	0.0023933	0.0345097	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814630	CTTTCTTGGTAAAAA[C/T]GTGTTAAAATACAGG	220441
rs186110731	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61817503	CTGCGACCAAATGAC[A/T]TCAAAAATACAGCGT	220441
rs186142320	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889464	AAAATCTCTGCAAGC[C/T]ACCAACTGCTGAATC	220441
rs186198505	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61837853	TCCTGGCTCACAGCA[A/G]CCAAATGCATTCTTT	220441
rs186250250	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61836969	ATATCAGCTCACAGA[C/T]TGCTTACTAAATGAT	220441
rs186286450	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879332	CTTTATAAGTAATCT[A/T]GTGACGATTTAAAGT	220441
rs186295469	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813361	GTACACAAATAACTG[C/T]AAGCAGATCCATTTA	220441
rs186300981	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61831321	GCTCGGGGAAATGCT[C/T]GGATTCATCATCTTT	220441
rs186394002	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896405	AATTTTTGTATTTTT[G/T]TATTTTTGTAGAGAT	220441
rs186397110	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61874242	CCGCAGTTTAACAGC[A/G]CATGAACTGACCAAA	220441
rs186402965	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852833	CTCCCCTAAAAAGTG[C/T]CTCACAGGTACTAAT	220441
rs186459934	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61860621	TAATTAACAACTATG[C/T]TACTGGTTTCTGCAT	220441
rs186631494	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869754	GTGGGCACACACACA[C/T]GCACGCACACACATG	220441
rs186648429	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61827696	TACCTACCCTCAATA[C/T]TGATGATTCATGGCA	220441
rs186653845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866136	GCTGAGTGGCACAGG[A/G]CCCCACCCCCTGTGG	220441
rs186659659	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61844136	AGAAAGAAAGAAAGA[A/G]AGAAATTAAGAGAAA	220441
rs186725725	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61823137	GCGTAGTCCAATTGA[C/T]GTAACTACAGTCATT	220441
rs186791485	snp	A/G	0.0126979	0.078662	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893945	GCCCCGCCAGACCCC[A/G]CGCTCCCCTCCCCGG	220441
rs186796860	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61872494	CTGGTTAAAAATTCA[A/G]AATTAACTCCTTGCA	220441
rs186805076	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850659	AGTTTGGATCATTTG[A/C]TATGAAAAAAATATA	220441
rs186842071	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61889122	GGTCTCCAAGCTGCT[C/T]ATCTCCCAATTCAGA	220441
rs186859025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847961	CTCTCACCACACTCA[C/T]GCTTCCCTTCGTGTG	220441
rs186979179	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61855356	AGTGATGGCAGAAGC[A/G]GCCTGTTTGGAGCAG	220441
rs187053972	snp	G/T	0.0103295	0.0711199	intron-variant	RNF152	GRCh38.p7	18:61820674	ACCCTCAATTGCAAA[G/T]GAGGCTGGGGACAAA	220441
rs187086280	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840374	TCAACATCTGTAAAA[C/T]CTCCTAGGATCCTGG	220441
rs187097160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849566	TGCACTGTTCCAAAA[C/T]ATGCAGAAAGAAATT	220441
rs187117814	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61885337	GTTTGAGACAGAGCC[A/T]CGGTCTTTTGCCCAG	220441
rs187135166	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61843211	ATTTTCTTTTCAACT[C/T]GTGCACACCCTACAG	220441
rs187161055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875604	GACCTGTCCACTCAA[C/T]GCTGCTTCTAAAGCA	220441
rs187164713	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832781	ACCCTGTGTTTAGAG[C/T]CCACCATATTATTAG	220441
rs187231813	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822743	ATTACATCGGGCTGA[C/T]CTTGAAGTGTTCCAT	220441
rs187295603	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61865772	AACTCACTTTAAGTT[A/G]AAGGCAAATATTCCC	220441
rs187369890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882208	AAATATTACAAAATC[C/T]AAAATCCAAAACATA	220441
rs187375465	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863338	TACTCGGGAGGCTGA[C/T]GCAGGAGAATCACTT	220441
rs187380966	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61841156	TAGAAATTCCTGCAG[A/G]GTTCCATACATGATA	220441
rs187453967	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877105	AACACAAAGCTTCCA[G/T]CCATCGAAAGACTCA	220441
rs187560056	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61833846	GGTGACCTCTCTCAA[C/T]TATAGCTACTTTCAT	220441
rs187566875	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808884	AGTGTGCTAACAATC[C/T]AAACCACGAGCATAG	220441
rs187604516	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815077	ACAATATTTACATTT[A/G]AAATTCTTATTTTGT	220441
rs187622475	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833379	TAGAAAGAAGGTGGA[A/G]GTAGCAAAGCCTCAA	220441
rs187660172	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61887212	CTTCCTCCCACAAGG[G/T]CAACTAAAAGTTATT	220441
rs187663264	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866711	TTCATCCCTTCATCA[A/C]CCATTCACTACTTCC	220441
rs187669736	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844260	AGGGCAGGCCCCATA[C/G]TATCTAGGAATCTAA	220441
rs187680558	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876267	TCCTATACCACCTGG[A/C]AATTGCATCCCTTTG	220441
rs187683986	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61855927	AAGAGAGTACACCTG[C/T]TAAGTATTCACTACT	220441
rs187715567	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61857167	GCATTATACGTCAGG[A/G]TTCAAGCTCTGTCTC	220441
rs187726785	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61885784	GGTAAAACAGATGTA[C/T]ATCACAAAGGTATTG	220441
rs187771621	snp	A/C	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61862534	AGGAATGCTAGTGTC[A/C]TGAAGCTTCGGTAAA	220441
rs187780278	snp	C/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61820257	TGGTGTGAACCCAGG[C/G]GGCGGAGCTTGCAAT	220441
rs187813232	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815543	TTTAACGTCTAAGTA[C/G]AATATGTCTATCTTG	220441
rs187833136	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810078	TACAGTAGAACCTAC[C/T]TCTTCATATATTTGA	220441
rs187955771	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887844	GATCAGAACTGAGCC[A/G]GGAAAGTTACACTTC	220441
rs187965838	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61868488	CCAAGGCGGGTGGAT[C/T]ACCCAAGAGTTTGAG	220441
rs187975392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847049	GCAAGGTATCCAGCC[C/T]AGTAGTGCACATAGT	220441
rs188041823	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881223	GGCCTTCTCTCTCTC[A/G]TTTTCTTATTTTCAC	220441
rs188059711	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839662	GCACTTTGGGAGGCT[A/G]AGGCGGGCGGATCAC	220441
rs188078020	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61881857	TCCTTCTCAGAGAAG[A/G]CATTTTTCCTTGTTA	220441
rs188122152	snp	A/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61825860	ATGTTCCCTACTCCT[A/T]ATTTTTTTTTTACTA	220441
rs188125811	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828475	TGTTGCCCAGGCTGA[A/G]GTGCAGTGACACAAT	220441
rs188169700	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863121	ACCAAATGTGTTGCC[C/T]GTAAAACATTTGCTC	220441
rs188218862	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871857	TAGTAAGCCTCTGAT[A/T]GGTACATATCTTCAT	220441
rs188317979	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61828988	TTTCAAGAAAAAGTA[C/T]CATTTCAATGTCAAG	220441
rs188337443	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813795	ACTTCTGTGGTGTGT[G/T]TGTGTGTGTATTTTC	220441
rs188345450	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61831435	AGTAGATGGCACACA[C/T]TGGGCACTAATTTAT	220441
rs188385673	snp	C/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61823687	CTGGCCCAGGTGGCA[C/G]AGGCAGGCAGGATGG	220441
rs188405582	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61874346	AACATATTGTATTTC[C/T]GATTACAGATACAGG	220441
rs188412116	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853807	TAATCACTTCCTTGA[A/T]GTCCCTTTTGCCATG	220441
rs188499270	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892861	GGAAATGGTACACGT[G/T]TAGGAGGCAAGAGGC	220441
rs188513449	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849927	ATCAAGTACTGTGTG[A/G]CCTGAGGCAATTCTC	220441
rs188594492	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810516	AGCTGGGCATGGAGG[C/T]GCATGCCTATAATCC	220441
rs188601745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884212	TAACTCAATGAGGTC[A/G]GTTCTCCCCCATTTT	220441
rs188611953	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61865119	TCAGTACCAGGAAAT[A/G]GAGGATGAAAACCAA	220441
rs188613936	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894821	AGTCTGTGCCTAGGA[C/T]CCGGACAGCGAGAGG	220441
rs188619813	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842336	CACAGTTCTATTAAT[G/T]GACAGCTGACCACAC	220441
rs188626309	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61873425	TCACCGCAACCTCTG[A/C]CTCCTGGGTTCAAGC	220441
rs188660723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822349	GGTCTTTGTGTTGTT[A/G]TTGCTGTTGTTATTT	220441
rs188678994	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844907	CACCTACTCGCCCCA[G/T]TGATTTACGATTTAT	220441
rs188858316	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61887590	CAGTAATCCCAGCTA[C/G]TCGAGAGGCTGAGGC	220441
rs188943847	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825270	CATGAGAAAGAGAGA[A/C]GGGTAGACAGAGCAC	220441
rs189026931	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61820991	CCACATACTTCCACA[C/G]AGTGAAAGGTTCAGA	220441
rs189043094	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813174	AGGGTCATTGGTAAA[C/T]GCCAGAAGAGGCCAG	220441
rs189070628	snp	C/T	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61869120	ATTTCCTAAGTTCAC[C/T]ATGTCTCTCTAAGTA	220441
rs189095456	snp	A/G	7.22256e-05	0.00600896	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816472	TCTCCATGGTGGACC[A/G]TGAGCAGGAAGGGCA	220441
rs189105697	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834629	ACTGGCACTCAGTAA[A/G]TGCTCAATAAATGCT	220441
rs189150964	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61867962	AACAAATATGCTAGC[C/T]AACACAAACAATATA	220441
rs189160571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878348	AGAATTATCCAGCCC[C/T]AGAGGTCAAAATGCT	220441
rs189164817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837229	GAAAACAAAAAGCAA[C/T]GAGATTGTTCTAGAT	220441
rs189208558	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821359	TTTATGCACTGATTT[G/T]TTCTACATGAAGCCA	220441
rs189318416	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863945	CGGCTGCCTTTTCCA[C/T]GTATTTTAATCTTTC	220441
rs189440240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817942	GAAAGAATTACTCAA[C/T]CACTATTGCAGAAAA	220441
rs189455375	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61859980	TGTCATTAGTTAAGA[C/T]GAGGTTATATTGGAG	220441
rs189465078	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812308	ACGGCACAGGTTTTC[A/G]AGCATTTCCATCATC	220441
rs189535994	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877912	GCCAAATGCAGTAAT[A/G]GTTTCTCTCTTCTTC	220441
rs189542554	snp	A/C	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61859377	TCGCATCAGTTTCAC[A/C]CACTGTTCCCAGGGC	220441
rs189568421	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816937	TTCTAAAATATACTA[A/G]AGAAACTTTCCTGCT	220441
rs189576863	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61835741	TACGCCTTTAGTGGG[A/G]TACATCCTTTAATAA	220441
rs189595865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883210	TGCAGCTTTCAAAAA[C/T]ATTTCTGAAGAATAA	220441
rs189611238	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61842096	AAACTAAATTCAGCT[C/G]TGAGTTTTATTAAGG	220441
rs189657373	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828426	CCAGCTACTTTTCCA[A/G]AAAACATTTTTTTGT	220441
rs189673323	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851003	AGAGAATCATGGCCA[C/T]TCCCCAGGGTACATA	220441
rs189793153	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874079	ATTAATTTAATTTTA[A/G]AAATATAAAAACTAA	220441
rs189809693	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889943	AATCAGCCTTGAAAA[G/T]ACCTAATGGCCTTTC	220441
rs189820350	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870710	ACTATGGTTTATGGA[C/T]CTCATTTCTTTGGGC	220441
rs189830527	snp	G/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61849087	GGGTTTGGGAGCCAA[G/T]TCTGTGTCAACCCGT	220441
rs189844229	snp	G/T	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809550	AAGGAGATTACAGAA[G/T]ACTTTCACATGGGCT	220441
rs189945432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830747	GATTGGCTGGAAGTA[C/T]AAAGAGCTGAGAGTG	220441
rs189967827	snp	A/C	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61831085	AAGGATGTGGAAGAG[A/C]CTATGAATCACAAAT	220441
rs190034559	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826495	TTCTCACCTTCCTCC[C/T]TTTCCCCTACTAAGT	220441
rs190053832	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852133	CAATTTTCAAAAACC[A/G]TGGCTTCTGGAAACA	220441
rs190128629	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61891814	GGAAAATGGTGAAGA[A/G]AGAATCTGTCACAGA	220441
rs190146477	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61858311	CCTCCCTCCCCCAAG[C/T]CCTCTGGAACTATCT	220441
rs190230657	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896028	GTTGTCCCTGGGATC[C/T]CAATTAAAACGTTGC	220441
rs190259801	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61886631	CCTGCACTAAGCAGG[C/T]CCAGGGTGAATGATA	220441
rs190270016	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866160	CCTGTGGTAACCCCT[A/G]CCCAAATCATCACAA	220441
rs190276667	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808113	CAAATGTGTTTTTAC[A/G]GTAGTCATAAAATCA	220441
rs190280129	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844191	AGAGAGGAAGGAAGG[A/G]AGGGAAGGAGGGAGG	220441
rs190314188	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61815053	ACACACACATACACA[C/T]ACAAATACACAATAT	220441
rs190321784	snp	A/C	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61833002	TGTCAAAGCAGAAGA[A/C]ACAGTAAGGCATACA	220441
rs190380908	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847459	AAAAATTCCCGCAAG[C/T]GTCCTTGAATCTGTT	220441
rs190384970	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877199	GAAACCATTTGACTT[A/C/T]CGTATTTTGGTCAGG	220441
rs190400720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823160	CAGTCATTGTTTTAA[C/T]GGAGCAGGACTTTGA	220441
rs190436221	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61889155	CGCTTTGGGTGCTAC[A/C]TCTTATCACTTGAAT	220441
rs190470838	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855489	TTGGGGCTCTGCAAT[C/T]CCTCGCATCTCCAAC	220441
rs190475033	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885034	ACTATTTATCCCAGT[C/T]AAGGACACCTCTTTA	220441
rs190485255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865498	TTACTAATCCATGTG[A/G]CAAACCTGGTTGGCA	220441
rs190495890	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61842682	TTACAAAAGAAAGAG[A/G]TTTAATGGACTCACA	220441
rs190561678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818577	TTACTGAAAGTGAAA[C/T]ACAGTAATGTAGCAT	220441
rs190570570	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61837995	CCTCTGATTTCTCAC[C/T]TCTGTGCCAGTCTTT	220441
rs190616120	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860627	ACAACTATGTTACTG[C/G]TTTCTGCATTTACTG	220441
rs190691058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869839	AACTTCCTCAGCTTT[C/T]ATGCATCCATGAACT	220441
rs190735557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881297	ACTATAGATTATAGC[A/G]AACGACACCAGTCAC	220441
rs190856385	snp	A/C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61822981	ATTTCAGCTGGCTTG[A/C/T]CAGCCACTTAGTTAT	220441
rs190887293	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61866059	TCATTCTTATGTCTG[C/T]GTGGAGGAACAGGCA	220441
rs190920801	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880610	ACAGTTATCTCCCCC[A/T]CTCTCCCAAATTGTC	220441
rs190929744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862279	TTTAATCTTCATGAC[A/G]ATGTGTGTGGCAGAG	220441
rs190989883	snp	A/G	0.0463947	0.145069	intron-variant	RNF152	GRCh38.p7	18:61862544	GTGTCATGAAGCTTC[A/G]GTAAAAAAACCCAAG	220441
rs191037981	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61839415	AACATCCCTCAGTTT[C/G]GGTTTGTGTGATGTT	220441
rs191076777	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61871385	AGCACCAGATACCTT[C/G]CAAGTGCTCCAACAC	220441
rs191127449	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812031	AAGCCCAGAAAGGAA[C/T]GTTTTGCCTTTTGCC	220441
rs191131585	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829867	TCTTGTAGGCTGTGG[A/G]GCTTGTGAAGACTTC	220441
rs191142288	snp	A/C	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61843220	TCAACTCGTGCACAC[A/C]CTACAGAAAAGCCAT	220441
rs191155446	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809135	ACTCTTCCTTTATTA[A/T]GTATTTTCTCCCTCT	220441
rs191212552	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894093	TCCCTGCGCACCCCT[C/T]TGTCCGCCCCCGATC	220441
rs191219117	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872610	AGGCCTCTTTCCCTT[C/T]TGGTTTGCCCTACAT	220441
rs191227048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850681	AAAAATATAAATTCA[A/G]GACAACAAAGTAAAC	220441
rs191234736	snp	A/G	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61854551	CTCTTTCTCAACTGA[A/G]CGAATTAAAGAGGGC	220441
rs191317433	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814001	CAAGAGCTTACACAA[G/T]AAAATGGCATTTTAA	220441
rs191372310	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815159	TTCTCATGATTTCTC[A/G]GTTTATTGCTCCCCT	220441
rs191380772	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61833405	CTCAAAGAATCCAAA[C/T]TTCAGGTGATTCACA	220441
rs191461836	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61874931	TGGTGAAAAAAAAAT[A/T]AGTAAGATGCTTGAG	220441
rs191545276	snp	A/G	0.00716266	0.059414	intron-variant	RNF152	GRCh38.p7	18:61876152	CCATTCCTCACTGCC[A/G]TGTGTCCAGACAATT	220441
rs191562768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832180	ATAATCAACACTTAA[C/T]AGTAATTTCTACCAG	220441
rs191668460	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881905	AGGACAGTGTGGACT[C/G]CCTTGAGATGCAATT	220441
rs191675615	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863250	CCATCCTGGCTAACA[C/G]AGTGAAATCCCATCT	220441
rs191676770	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61828541	GTGGTCCTTCCATCC[C/T]AGCCTCCAGAGTAGC	220441
rs191683184	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61840813	CAGTGTAGCATGTAC[C/G]TTTCTAGGTTTGTGG	220441
rs191692230	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61820675	CCCTCAATTGCAAAT[C/G]AGGCTGGGGACAAAA	220441
rs191847897	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822540	GCAAAGATCTCCAAC[A/G]TTGAATTTTTATAAT	220441
rs191860008	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888086	TTGCAATGAGTTTTA[C/T]TTATGCAGGCATTAG	220441
rs191958829	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810362	TAGAAGTGTTTCATG[A/T]TGGCTGGGTGCAGTG	220441
rs191982386	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61849627	AAACTATGGTTTTAG[A/G]TTATCCAAAACAAAA	220441
rs192008219	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816674	TATCTAATGGATTTA[A/T]ACCATTGCTCAAAAG	220441
rs192014619	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834963	CTGCAAAAAGGCAAC[A/G]TTCCCTGGGTGATTC	220441
rs192016923	snp	A/T	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61848558	CTCAGCCTAACACAG[A/T]TACCTTCTTAGTAGT	220441
rs192078776	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819482	AATGAGTAGCTGAAG[A/T]GAATAGTGATGATTA	220441
rs192082207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877222	TGGTCAGGGGTTCTG[C/T]GTAGACACAATGACA	220441
rs192089343	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858410	CAGCCCTTCCCTCCC[A/C]CAAGCTCTCTGGACC	220441
rs192100294	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61887432	ATAGTAAGAAGAATG[C/T]TCCTGGCTAGGTGCG	220441
rs192181105	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61885338	TTTGAGACAGAGCCT[C/T]GGTCTTTTGCCCAGG	220441
rs192227187	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61879863	CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT	220441
rs192285159	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840184	TGTGTGACCAGGAAA[C/T]GGGCTCTTACCAGAC	220441
rs192380247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876331	TAAAGGAGCATCTTG[A/G]TATAAAAATAACCAA	220441
rs192388493	snp	A/C/G	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61855997	CCAGGTACTTAAAGA[A/C/G]CTCTGTGTTCTAGTC	220441
rs192428501	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61828139	TATTTCCGCCACCCC[A/G]AAAGGTCCCCTTGTG	220441
rs192572611	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873616	TGGGATTACAGGCAT[A/G]AGCCACCACGCCCAG	220441
rs192647010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830756	GAAGTACAAAGAGCT[A/G]AGAGTGAAGGAGTAT	220441
rs192658140	snp	A/G	0.00716266	0.059414	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810580	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	220441
rs192695719	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61882464	CATGGGAAAGAGGCA[C/T]GCAAGTGTCTGGCAA	220441
rs192709810	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863551	GGAAATAGTTAATAT[A/C]TTTGGGGAAAAAACT	220441
rs192712390	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857331	TGCTCTGGAAACCAC[A/T]CACTATGTCCACATG	220441
rs192838998	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895136	TAGAATGTCTTGTTC[C/T]CCGGAGAAAATCTCC	220441
rs192846383	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61851324	CTCTGCATAAACACT[A/G]CATCTATACCATATT	220441
rs192881556	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844717	GTAACCATAGCACGG[A/G]TCGGTAGGTCATATG	220441
rs192913049	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877154	CTCCCACAAACAACT[A/C/T]GGCTGTTGTCATCCA	220441
rs193001679	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61834122	TTTGTTACGTCCTGG[C/T]TTGAATCCCACACTC	220441
rs193028047	snp	A/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61824794	GCTGGCATTCATCAA[A/T]CACATGGCTTTATCT	220441
rs193034774	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868130	TCCAGTCATTTTCCT[C/T]GTAGCCAGCACAGGC	220441
rs193059592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825381	GAACTATCATTGCCT[A/G]TCAGAGCCAGAAAGG	220441
rs193083825	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867431	CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACACC	220441
rs193099914	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893114	ATAACCACCTCCCCC[C/T]TCCTCCGCAGTCTCC	220441
rs193103411	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61850225	ATGCCCCTTGTCAGT[A/G]AAGTGTGAACACTAA	220441
rs193148202	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61821212	TGCAATTTTATTCAT[C/G]AATTTATGTTCCAAG	220441
rs193219406	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887675	CCACTGCACTCCAGC[A/C]TGGGTGACAGAGTGA	220441
rs193222909	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61844977	TCCTTCCATTCCTCC[C/T]GAGGGCCATAAGTGG	220441
rs193255615	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841314	AAATATCTCCAGACC[C/T]GCAACATAACATGAC	220441
rs193256917	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872037	CAGGCTGTACAGTAA[G/T]CATGATGTTGGCATC	220441
rs199521602	snp	A/C/G	0.00014485	0.00850916	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816474	TCCATGGTGGACCGT[A/C/G]AGCAGGAAGGGCAAG	220441
rs199543439	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61830231	GGTGTCTTGGTATTT[A/G]GCCAGGCTGGTCTTG	220441
rs199573948	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61870877	CATCACACACATTGC[-/AG]ACCCATGATTCCATC	220441
rs199636346	in-del	-/CTC	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61881021	GGGGTTCAAGCGATT[-/CTC]CCATCTCAGCCTCCC	220441
rs199771463	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61884682	TTCCTGCCTCAGCCT[-/C]CAGAGTAGCTAGGAT	220441
rs199853701	snp	A/G	0.000148619	0.00861902	synonymous-codon	RNF152	GRCh38.p7	18:61816122	GCAGCCCATGTCTCC[A/G]GGCAGCAGCGCACGC	220441
rs199861568	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61851391	AGAGGGGAGGGAGGA[C/T]GGAAAAGAGGAGAAA	220441
rs200181771	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61839055	TCCCACTCTGTGGCC[-/AA]AAAAAAAAAAAAAAA	220441
rs200205280	in-del	-/AA/AG			intron-variant	RNF152	GRCh38.p7	18:61844109	AAAGAAAGAAAGAAA[-/AA/AG]GAAAGAAAGAAAGAA	220441
rs200219405	snp	C/T	0.000296941	0.0121812	missense	RNF152	GRCh38.p7	18:61816070	CAGGGATGGTCACCA[C/T]GGTGACGGACTTCTG	220441
rs200310382	in-del	-/TCC	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61826489	AGGCCTTTCTCACCT[-/TCC]TCCCTTTCCCCTACT	220441
rs200330870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884219	ATGAGGTCGGTTCTC[C/T]CCCATTTTGCAGCTG	220441
rs200335990	snp	C/T	1.74903e-05	0.00295717	missense	RNF152	GRCh38.p7	18:61816447	TCCAGCAGAGAGTCC[C/T]GGGACAGCGTCTCCA	220441
rs200396726	snp	A/C/T			intron-variant	RNF152	GRCh38.p7	18:61882846	AGTAAACACTGGGTG[A/C/T]TGAGTACACAATGCC	220441
rs200521489	in-del	-/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61875644	TTTCTCCCAAATCTG[-/T]TTTTTTCCCTGCAAT	220441
rs200550326	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61844220	GGGAAGGAGGGAGGG[-/A]AGGAGGGAGACGGGA	220441
rs200569440	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847184	ATAAAAAGCAAGAAG[C/T]GGAGAGAACAACACA	220441
rs200699783	in-del	-/TG			intron-variant	RNF152	GRCh38.p7	18:61831916	ATAAATATAGTATTA[-/TG]TGTGTGGGGGGGTGT	220441
rs200774584	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896147	CATGTTTTAGAAGCC[C/T]AAGGTAATCCTGAAG	220441
rs200817499	in-del	-/AGAG			intron-variant	RNF152	GRCh38.p7	18:61844176	GGGAGGAAGGGAGGA[-/AGAG]AGGAAGGAAGGAAGG	220441
rs200819394	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820145	CCATCCTGGCTAATA[C/T]GGTGAAACCCCGTCT	220441
rs200839055	snp	G/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61828568	TAGCTGGGACTACAG[G/T]TGTACACCATTGCAC	220441
rs200924436	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879365	ACACGAGGAAGTGCA[C/T]AGGTTATATGCAAAA	220441
rs200953577	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887490	TTGGGAGCCCAAGGC[A/G]GGTGGATCACGAGGT	220441
rs201105856	in-del	-/A	0.389903	0.207189	intron-variant	RNF152	GRCh38.p7	18:61839055	TCCCACTCTGTGGCC[-/A]AAAAAAAAAAAAAAA	220441
rs201151396	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61884444	TTAGCTTTGCCATTA[A/C]AAAAAAAAAAAAAAG	220441
rs201163137	in-del	-/T	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61879296	TACATTACATTTGCA[-/T]AGCATTTACATTGTA	220441
rs201297490	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829656	GAAGAGGGGAGGACC[A/G]GGAGGTGAGGGGAGA	220441
rs201307914	snp	A/G	1.64808e-05	0.00287057	missense	RNF152	GRCh38.p7	18:61815895	TTAGAAATGCAAGAC[A/G]TGTTGTGAAGCACGA	220441
rs201393198	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61864487	GGCGTCACCCTCCCC[A/C]AGCTCCTCAAAGTGT	220441
rs201462556	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61831781	ACATGTTAATTACTT[C/T]TATTTTAAAAAGTGT	220441
rs201511657	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61828251	TTTTCTTCCTTCCTT[C/T]CTTTTTTAAGAGACG	220441
rs201560722	in-del	-/GAAA			intron-variant	RNF152	GRCh38.p7	18:61844141	AAAGAAAGAAAGAAA[-/GAAA]TTAAGAGAAAAGGAA	220441
rs201706905	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887234	AAAGTTATTAAGTGA[A/G]GGGATGAAGGATTAA	220441
rs201778796	in-del	-/AAAG			intron-variant	RNF152	GRCh38.p7	18:61844021	AAGGAGAATGAGAGA[-/AAAG]AAAGAGAGAGAGAAA	220441
rs201825588	snp	C/T			missense	RNF152	GRCh38.p7	18:61816177	ATGTAGCACCCATTG[C/T]TGGGAAGTTTGATGA	220441
rs201903258	in-del	-/A	0.0119091	0.0762411	intron-variant	RNF152	GRCh38.p7	18:61831615	TTTAAGATGTAAGAT[-/A]AAAAAAAATAAGCAA	220441
rs202002174	in-del	-/CC			intron-variant	RNF152	GRCh38.p7	18:61820330	AGAGACTCCGTCTCA[-/CC]AAAAAAAAAAAAAAA	220441
rs202028108	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829596	AGAGAGAGAGAGATA[A/G]GGAGAGAGAGAGAGA	220441
rs202033474	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872779	TGAATTTCTGGTATA[A/C/G]AAACAAAACAGCCAT	220441
rs202122698	in-del	-/T	0.0142736	0.0832652	downstream-variant-500B	RNF152	GRCh38.p7	18:61808012	GAAAATCTCAGCCAA[-/T]TTTTTTTTCTTTTCC	220441
rs202181235	snp	G/T	0.000568573	0.0168512	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816485	CCGTGAGCAGGAAGG[G/T]CAAGGCCAAGGTGAA	220441
rs367545843	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61829654	GTGAAGAGGGGAGGA[C/T]CAGGAGGTGAGGGGA	220441
rs367556967	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844462	TGCTTCACCTTGGCA[A/C]AAGAAAACCATCCAT	220441
rs367558080	snp	G/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61862755	CAAGTTCTGTGAGCC[G/T]CTCCAGCAAATTCAT	220441
rs367799726	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866274	GCCCAGGTAGCCCCA[C/T]GGATGGCTACTCCCC	220441
rs367808470	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829997	CCATCATGTGTAGCC[A/G]TCGTCCCCATCTATT	220441
rs367863712	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883397	TCTTTTTAATAATAA[G/T]AAATATCCCATTCCA	220441
rs367867236	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61861688	AAGGTTCAAGACTCG[A/G]CATTTGGCGAGGGCC	220441
rs367914697	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61840113	AATGTAACCTAAAGG[C/T]CCAAGGGAGCTTATT	220441
rs367926396	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896103	GCTAAAACCTCCTTC[A/G]TACACCTGAAAAGAG	220441
rs367989643	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61851451	GCTTCAGGGGTGAGG[C/T]TACAGTGAGACACTC	220441
rs368000636	snp	A/G			missense	RNF152	GRCh38.p7	18:61816102	TGGCTCCCGGGCAGC[A/G]GGCGGCAGCCCATGT	220441
rs368035264	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61836677	GTTGTTTTGTTATGG[A/C]AGCCCAAGCTAGCTA	220441
rs368059332	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809158	CTCCCTCTTTGGGTA[C/T]ATCTGCCTGTCCCTT	220441
rs368069525	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875779	GAAATGTCTCTTGCA[C/T]TGATTCACCCTCCCA	220441
rs368087652	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829562	TGGGAGAGGGAGAGA[A/G]AGAGATTGGGGGAAG	220441
rs368110873	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61833286	GACAGCCAGTCTATT[C/T]CAGAAAATAATTCTC	220441
rs368130398	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61892294	ATGTCTCTCTTAATA[C/T]TGCAAACACTATTAC	220441
rs368144289	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61826912	CTTTGTTTTTAAATA[A/G]CTGTTTCCAGACAAC	220441
rs368180490	snp	A/G	1.64933e-05	0.00287165	missense	RNF152	GRCh38.p7	18:61816205	TGAAGACCGGGGTGT[A/G]TTCGGAAGTGTGTGG	220441
rs368191771	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61880144	CCTGAATTAGCACAG[A/G]ACAAAACTCAGGTAA	220441
rs368197318	in-del	-/T	0.162909	0.23434	intron-variant	RNF152	GRCh38.p7	18:61831920	ATATAGTATTATGTG[-/T]GTGGGGGGGTGTGGG	220441
rs368246696	snp	C/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61866546	CCCCAGCAGGGCCTA[C/G]GCATCCTTTGGTGAC	220441
rs368368636	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861377	GCTTGCAGTATTCAG[C/T]ATAATAATATGCTGT	220441
rs368368875	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61879076	TGGGAACAAAGTATC[G/T]AAGAAAGTACAGTCT	220441
rs368486975	in-del	-/CTCTCACACA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813275	TCTCTCTCTCTCTCT[-/CTCTCACACA]CACACACACACACAC	220441
rs368497453	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61889360	CACTTATGCTTAAGG[C/T]ATTTATCAAATCTTT	220441
rs368499867	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829373	TCTGCCAGCCCCAGC[A/G]CTCTAAAGCAGGGGG	220441
rs368514657	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61875405	ACATCAAATTTAATT[C/G]TCAGTGCATGCAAGT	220441
rs368541652	in-del	-/CACTCAC			intron-variant	RNF152	GRCh38.p7	18:61861203	ATCACATCCACTCAC[-/CACTCAC]ATCCTGAATCACTCA	220441
rs368598527	snp	A/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61880638	GTCTTTTGGTTGTCA[A/T]GAAATACATTGCGGA	220441
rs368706136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871676	TGGTATCCCGATGCC[A/G]AGCCTTCAGAAGGTA	220441
rs368744715	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890759	GAGGGTGCTGACAGC[A/G]TAGGTGGGTTCAAAC	220441
rs368749724	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61873131	ACTGTGCTTTCTGTC[A/T]GCCCATCAAAAAATA	220441
rs368763426	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61821111	CAAAGAGCTGCCACT[C/T]GGAACAGCTTGGGAG	220441
rs368767989	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853428	CTGAGTAGCTGAGAC[C/T]ACAGGCACATGCCAC	220441
rs368902239	in-del	-/AACA/G	0.0056132	0.0526792	intron-variant	RNF152	GRCh38.p7	18:61831684	CCTCAAAGCAGAACA[-/AACA/G]AACAAACAAACAAAC	220441
rs368973806	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61848159	TGATTTCAAAAGCGC[C/T]TCTGGGCTCCTCTCA	220441
rs368983390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858973	GGGGAAACTCCATGT[C/T]TCTTACGCGCCGGGT	220441
rs368994028	snp	A/G	6.59055e-05	0.00574007	synonymous-codon	RNF152	GRCh38.p7	18:61815909	CATGTTGTGAAGCAC[A/G]ATGCCGAGGAGGAAG	220441
rs369042071	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872640	TTTGAAAAGCATTTG[C/T]CATTCTACTGTAGTG	220441
rs369074452	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61879922	GTGAGCCGAGATCCC[A/G]CCATTGCACTCCAGC	220441
rs369082532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822084	AGTACTTCAGTAGAA[C/T]GCATAAGAACAAGTA	220441
rs369227860	in-del	-/GT			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810273	TACAGCTAAATCGTG[-/GT]GTGTGTGTGTGTGTG	220441
rs369352962	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61886460	TTTTCACTTTCAATA[-/CA]GTATTCAATAAACTA	220441
rs369354292	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863327	GTAGTCCCAGCTACT[C/T]GGGAGGCTGACGCAG	220441
rs369354915	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817346	TTTTTGTTTCATTAC[C/T]ACTTAGGCTTGTACC	220441
rs369384906	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879889	AGAATCGCTTGAACC[C/T]AGGAGGCAGAGGTTG	220441
rs369510834	in-del	-/C	0.0693013	0.172766	intron-variant	RNF152	GRCh38.p7	18:61845928	CTTTGTGTGGGGGGG[-/C]GTGGTGATGAGGACT	220441
rs369518374	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847323	GCATGGGGTCTGCTT[C/T]TGTGGGCGACTTGAA	220441
rs369575337	in-del	-/CTC	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61885173	CCAACCACTTCTAAT[-/CTC]ATATTATTAATCTTC	220441
rs369621346	snp	A/C	8.25266e-05	0.00642312	missense	RNF152	GRCh38.p7	18:61816140	CAGCAGCGCACGCTC[A/C]TTGGAGATGGGCAGG	220441
rs369636937	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879846	GGCGCACGCCTGTAA[C/T]CCCAGCTACTCAGGA	220441
rs369686940	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61846683	AAACACCTGGCACCA[C/G]AAAGGTATTCTGTAC	220441
rs369693567	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866812	CTGTCCCCACCGCTG[A/C]GCAGCACATGACAAG	220441
rs369709063	snp	C/G	7.48153e-05	0.00611572	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816514	AAGGGGAAGGAGCTG[C/G]TTCTCAGAGGCCACC	220441
rs369709759	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884088	AATGATTGGTGGATG[A/G]TAGATGCTGGATATA	220441
rs369856736	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61860453	GCTGGAAAATTCCTA[C/T]TGCCTGGTGATACAG	220441
rs369869989	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874265	TGACCAAAGAGAAGA[A/C]TCCATCAAGGTAGTT	220441
rs369880895	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61833252	AGGTCGCAAGAATCA[A/G]ATTAAATTGGTTTAT	220441
rs369941240	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827303	GGAACATTGAATAAA[C/T]TGCCCAAACACATTC	220441
rs369977363	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61892500	TCTATGGAAACCTAA[-/CA]TTCAGATACAACTGC	220441
rs370094283	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824889	GAGCTATAAAAGACT[A/G]TCAGGAGATCCCCAG	220441
rs370148283	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61819221	AATAAAACTCTCAGA[C/G]AACCTGCAAGCACTC	220441
rs370212126	snp	A/C	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61829102	CCTGGGACCTCCAGT[A/C]AGTCAAATACCCCTG	220441
rs370262709	snp	C/T	0.000153988	0.00877328	missense	RNF152	GRCh38.p7	18:61816268	CCGGGAGCTGCGACA[C/T]GGAGAAGCCGGGAGG	220441
rs370346839	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860143	GAGAAGCTGGGGAAG[G/T]GAGGAAGGGTTCTCC	220441
rs370362019	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61891660	CAACTGCTTTTACTA[C/G]TGACTCCTGAATGCT	220441
rs370387208	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810753	AAAACAGCTACTGAA[C/T]TATCTCGACTATCTT	220441
rs370494806	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879781	CCAGCCTGACCAACA[C/T]GGAGAAACCCCATCT	220441
rs370621386	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61848391	GCCTCAAAGAGAAGC[C/T]CTAGGTTTATATGTC	220441
rs370624623	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61866455	TCACATCCACACTCT[C/G]GCCCGCGTTTCTGTG	220441
rs370685370	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61823895	GCCGTGGAGCCAAGG[G/T]CATCCTGTGCCAGGG	220441
rs370747962	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61868532	ACGTGGTAAAATCCC[A/G]TCTCTACTAAAACTA	220441
rs370754248	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832581	AAAAAATTCTCAATA[A/G]CTTATCTTTCTCAGG	220441
rs370990559	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865182	TACCCCTAGAACCTG[C/T]AGCCAAATTGTCCGG	220441
rs371019793	snp	C/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893181	ACTAGCAACAGTAAG[C/G]CCTAGGAAAGAAAGA	220441
rs371021123	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878792	CATTAATCCCATTCA[C/T]AAGGGCAGAGCCTTC	220441
rs371073949	snp	C/T	9.88566e-05	0.00702983	missense	RNF152	GRCh38.p7	18:61815986	TGGAGCTTTTCACCA[C/T]GCCCCGCCTGTCCTG	220441
rs371124692	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61879092	AAGAAAGTACAGTCT[A/G]CCCTCCATATCTGGG	220441
rs371145140	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61887553	GAAACCCTGTCTCTA[A/C]TAAAAATAGAAAAAA	220441
rs371147540	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61887543	CCAACATGATGAAAC[A/C]CTGTCTCTACTAAAA	220441
rs371241499	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812089	TCACCTTAGCCTCAC[G/T]GTTACTCCATTAATA	220441
rs371340855	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844272	ATAGTATCTAGGAAT[A/C]TAAAAAGCTCAAAGT	220441
rs371346822	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61842862	ATCACAAGAACAGCA[-/C]GGGAAAGACCCGCCC	220441
rs371354675	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811623	CTGGCCAACTTCAAG[A/G]GCAAACAAAACCAGT	220441
rs371411283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826857	GTTTTCAAAATTATT[A/G]TGCATTCTATTTTGG	220441
rs371471017	snp	G/T	3.29511e-05	0.00405887	stop-gained	RNF152	GRCh38.p7	18:61815933	GAGGAAGACCAAGAC[G/T]CAAGCCACCAAGATG	220441
rs371597317	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812739	GTTTTACAATTTTAA[A/C]AATTCAAACCACATG	220441
rs371734132	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823381	GCTCACCGCAACCTC[C/T]GCTTCTTGGGTCCAG	220441
rs371748022	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61875667	CCTGCAATTTTATAT[A/C]CGTTACCATTATTTA	220441
rs371753536	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820442	AAAATACAGGGTTCG[C/T]TGGTGAATCCTGCTC	220441
rs371786067	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61883891	TCATTTTAAACTCAG[A/G]GCCACTGAAAGCTTT	220441
rs371946660	snp	C/T	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61847032	TTAAATGGGGGTAAG[C/T]AGCAAGGTATCCAGC	220441
rs371956743	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833369	TAACCTACATTAGAA[A/G]GAAGGTGGAGGTAGC	220441
rs371960301	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61836685	GTTATGGCAGCCCAA[A/G]CTAGCTAAGACAGAT	220441
rs371961590	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884597	ACAGTCTCATTCTGT[C/T]GCCCAGGCTGGAGTG	220441
rs372025032	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831684	CCCTCAAAGCAGAAC[A/G]AACAAACAAACAAAC	220441
rs372035513	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844121	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs372042625	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61826949	GAGCTGAGCAAAGAA[C/T]ATAAACAATGGCCAT	220441
rs372095491	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844715	GTGTAACCATAGCAC[A/G]GGTCGGTAGGTCATA	220441
rs372103990	in-del	-/GC			intron-variant	RNF152	GRCh38.p7	18:61885980	CTTTTGCTTTCTTTT[-/GC]TTTCTTTTTTTTTTT	220441
rs372151508	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894009	AGAAGATCTCCCCAG[G/T]TACAGCAGGCGGCAG	220441
rs372193843	in-del	-/GAG			intron-variant	RNF152	GRCh38.p7	18:61881457	CTCTGATGGGAAGAG[-/GAG]AAGTGCAGATGGCAG	220441
rs372303338	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888784	ACACAGTGTAACTCT[C/T]GAAGCCATGGGAAAA	220441
rs372308542	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831680	GCTACCCTCAAAGCA[A/G]AACAAACAAACAAAC	220441
rs372358964	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61840072	TCACTGCTCCCATGC[A/G]TGCCCATGGGCACAG	220441
rs372363087	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879235	GCTAAACGATACAGT[A/G]TAACAACAACTTACA	220441
rs372462487	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61875687	ACCATTATTTACCCA[A/C]TACCTCAGACTTGAA	220441
rs372529972	multinucleotide-polymorphism	CC/GA			intron-variant	RNF152	GRCh38.p7	18:61870879	ATCACACACATTGCA[CC/GA]CATGATTCCATCCCC	220441
rs372542736	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61855995	AACCAGGTACTTAAA[A/G]AACTCTGTGTTCTAG	220441
rs372632579	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877629	GCTTGTTAATCACAC[A/G]TCAAAATTATTAGGG	220441
rs372753297	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61861093	TACAGTAAGCTAAGA[C/T]TATTATTGAAGAAAA	220441
rs372803025	snp	A/G	0.000153988	0.00877328	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816479	GGTGGACCGTGAGCA[A/G]GAAGGGCAAGGCCAA	220441
rs372908375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864676	CAGAGTTGGTTCCTC[C/T]GGCGACCAGCTGGCA	220441
rs372938430	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859603	TGACACCTAGGCCGG[A/G]CACGGTGGCTCATGC	220441
rs373011013	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61848309	TCAATATTTTTGCAA[A/G]ATATCAGTGCTTCCA	220441
rs373015019	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61873493	CAGGCACGCCACCAC[A/G]CCTGGCTAATTTTGT	220441
rs373020635	in-del	-/TTTTCCCCT	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61854339	GGTCATGTAAGAAAG[-/TTTTCCCCT]TATATGGGGGAAAAA	220441
rs373072212	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858979	ACTCCATGTTTCTTA[C/T]GCGCCGGGTGATGTC	220441
rs373116399	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810936	TGGTGGGCAGCATCA[C/T]TTTTCTGAGAAAAGA	220441
rs373120322	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61863263	CACAGTGAAATCCCA[C/T]CTCTACTAAAAATAC	220441
rs373152645	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61887131	GGCGGAGCAAAAGTC[A/G]AGGTTGGAAAGGAAG	220441
rs373156416	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61823519	GGCCAGGCTGGTCTC[A/G]AACTCCTGACTTCAA	220441
rs373170090	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827917	AAACTAGATATGGAA[C/T]AGCGGTGCAACCCAA	220441
rs373200252	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894953	GCCCCGCTTTCCAAA[A/G]AGGCCCGAATGGACA	220441
rs373227259	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879890	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	220441
rs373230699	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814398	TGTCACATACCACTT[C/G]CTTCATGAATTCCAT	220441
rs373259832	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61878865	ATCTTGGGGTTTAAA[C/T]TCCAACATGAATTTT	220441
rs373268122	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61879848	CGCACGCCTGTAACC[A/C]CAGCTACTCAGGAGG	220441
rs373293768	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818900	CTAGAGATGGGAGCG[C/T]TAAGTACTTAGACAA	220441
rs373347132	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61817380	TAACACAACTAAAAG[C/G]AAGTACGATTGACCC	220441
rs373404623	in-del	-/CTAGCAACAGTAAGCCCTA			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893167	GTGGCAGAGCGCCTA[-/CTAGCAACAGTAAGCCCTA]GGAAAGAAAGAAATC	220441
rs373450871	snp	C/T	0.00953873	0.0683987	intron-variant	RNF152	GRCh38.p7	18:61867566	AGGAGTTTGGTTGTT[C/T]TGTTTTTTATTTTTT	220441
rs373488894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854936	TTTTCCTGAACTACA[A/G]ATAACTCACAGACTG	220441
rs373500965	snp	A/G	8.24994e-05	0.00642206	synonymous-codon	RNF152	GRCh38.p7	18:61816071	AGGGATGGTCACCAC[A/G]GTGACGGACTTCTGC	220441
rs373554233	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61838803	AAGTCTTCACCCAGC[C/G]TTTTCTCATGACTTG	220441
rs373570269	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878171	GTACAGAAAGTAGTA[C/T]AGTCGAGTGATTGTC	220441
rs373641819	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813593	GGACACTATCATCAC[A/T]CACATTAGTGTCTAT	220441
rs373645415	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61826878	TCTATTTTGGAGATA[A/G]TAAGGCTTACAGATG	220441
rs373656925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857987	TTAGCTTTACGTTTG[A/G]GTCTCCTCTGCTATA	220441
rs373675676	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61877600	TCTACTGAAAGTATT[C/T]ATAGCTCAAAGCTGC	220441
rs373801843	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61834813	TAAGTTACTTAAAAG[A/G]AAGAGTTACTAGGTA	220441
rs373814821	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879273	TGTGTTTACATTTAC[A/G]TCATGTTTACATTAC	220441
rs373907070	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866086	GGCAGGAATATTCCT[A/G]GCCATATACTCCCAC	220441
rs374000077	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61862914	CTCTGACATTATCTC[G/T]GGGTAGACACTGTTG	220441
rs374092992	snp	A/C			missense	RNF152	GRCh38.p7	18:61816067	CAGCAGGGATGGTCA[A/C]CACGGTGACGGACTT	220441
rs374155215	snp	C/G	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61860256	GTTTGAAGCCACCTA[C/G]TTGGTTAAGGCAGCC	220441
rs374278354	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61819497	TGAATAGTGATGATT[A/G]GGACAGAATGATGAG	220441
rs374318370	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61886547	CCCATTGTAGGCTAA[C/T]TGCAGGTCACAACTG	220441
rs374320447	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61832513	CCCTGTAGAATTAAG[A/C]CTGTTTAATCCACAA	220441
rs374414264	in-del	AAA/T			intron-variant	RNF152	GRCh38.p7	18:61884451	TGCCATTACAAAAAA[AAA/T]AAAAAGCAGAAAACC	220441
rs374468879	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872346	AACCACATCAGGTAG[C/T]AAACCTGATCGCTGA	220441
rs374531673	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61862354	AAGGCTCAGTTGGAT[C/G]AGGGACTGCCCAGAG	220441
rs374609206	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61873180	TACTCCTAATTATTA[C/T]GAGAATGAAATTGGG	220441
rs374731169	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61856784	GGGATTCAGTTCCCC[A/G]AACAGCTAGCTCCAT	220441
rs374740602	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61879966	GCGAAACTCCATCTC[-/AA]AAAAAAAAAAAAAAT	220441
rs374741217	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61881876	TTTTCCTTGTTAATT[A/C]ACAGTCTTCTTATAG	220441
rs374750793	in-del	-/TGCAGTGAGCTGAGCTCGT			intron-variant	RNF152	GRCh38.p7	18:61864976	GTGAGCTGAGCTCGT[-/TGCAGTGAGCTGAGCTCGT]GCCATTGCACTCCAG	220441
rs374977073	snp	A/G	0.000132055	0.00812465	synonymous-codon	RNF152	GRCh38.p7	18:61816269	CGGGAGCTGCGACAC[A/G]GAGAAGCCGGGAGGC	220441
rs375018831	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61878101	CCCACTCTGAACTGC[A/G]TCTCATTTCCATATA	220441
rs375073973	in-del	-/AAAAAAA			intron-variant	RNF152	GRCh38.p7	18:61877551	ATACACAGTGAAATG[-/AAAAAAA]AAAACTGCCAGTACA	220441
rs375104791	snp	C/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61868340	TCAGAGACCACAGGA[C/G]AGAGGTAAACCCAGC	220441
rs375108516	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61867413	GAGGAGACTGCGCCA[C/T]TGCACTCCAGCCTGG	220441
rs375117185	in-del	-/AACATGGAA	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61832950	TTTATAAGTACCTAT[-/AACATGGAA]AATCTGTATCTGCTT	220441
rs375129292	snp	A/G/T	0.00478372	0.0487162	intron-variant	RNF152	GRCh38.p7	18:61863296	AAAAATTAGCCAGGC[A/G/T]TGGTGACACACGCCT	220441
rs375174367	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837413	GTGATAATGGTGCGA[C/T]TATGTAAGAGAATGT	220441
rs375228146	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836047	TAAATTTCTAAGCCT[C/T]GTCAACTGAAAGGCC	220441
rs375298877	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815850	CTTCCCTGCAGCCCT[C/T]TTCAGCCACAGGATA	220441
rs375367742	snp	G/T	1.64787e-05	0.00287038	synonymous-codon	RNF152	GRCh38.p7	18:61815992	TTTTCACCACGCCCC[G/T]CCTGTCCTGCTCCTC	220441
rs375374406	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61863113	CAAAACAAACCAAAT[C/G]TGTTGCCCGTAAAAC	220441
rs375383403	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889066	CAACCCCAGGCACCC[C/T]GAATGGGTTTTTGGA	220441
rs375491495	in-del	-/AGGGAAGGAGGG/AGGGAAGGAGGGAGGGAAGGAGGG/GGG			intron-variant	RNF152	GRCh38.p7	18:61844191	GAGAGGAAGGAAGGA[lengthTooLong]AGGGAAGGAGGGAGG	220441
rs375499397	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883068	GAGCATATCTAGATG[C/G]ATGCATTTTCAAATG	220441
rs375541546	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813239	TAAGCCTATAAAATT[A/C]TATCTGGGAGACTGA	220441
rs375671319	snp	A/C/G	0.0718919	0.175435	intron-variant	RNF152	GRCh38.p7	18:61866460	TCCACACTCTCGCCC[A/C/G]CGTTTCTGTGCTTTG	220441
rs375681546	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875278	GGGTCCTATATGGAA[C/T]AGTCCTTAAGCACCG	220441
rs375744481	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886940	GGCTAATGTGATCAA[A/G]TTAAATTTTTCAGAA	220441
rs375746978	snp	C/G			downstream-variant-500B	RNF152	GRCh38.p7	18:61807992	ATCCTTAGAATAACT[C/G]ATGATGAAAATCTCA	220441
rs375748318	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61862520	TGTGCCCTGGGGACA[C/G]GAATGCTAGTGTCAT	220441
rs375759967	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61833639	GTTAGTCTCGTCTGT[C/T]TGTTTTTCTTTAGCT	220441
rs375827642	snp	G/T	0.386504	0.209444	intron-variant	RNF152	GRCh38.p7	18:61829508	GGGGAGAGAGAGATA[G/T]ATATATATCAGGGGA	220441
rs375855905	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858985	TGTTTCTTACGCGCC[A/G]GGTGATGTCAATATC	220441
rs375864147	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61830673	AGAGGCTGAACTAAA[A/G]GAAAGAGGGGCAAGG	220441
rs375881391	snp	A/C/G	0.0119135	0.0762987	upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894466	ACTCCGGCACCAAAG[A/C/G]GGGTGGGGGGAGAGG	220441
rs375909524	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844113	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs375943078	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61860022	CTTAATCCAACATGA[C/T]TAGTGTCCTTTAATA	220441
rs376041142	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846013	CTTATCTCGTTCCAC[C/T]ATGTGAGGACACAGC	220441
rs376156120	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61844882	AAACAAAAAAAAAAA[-/A]GCATTTATTCACCTA	220441
rs376241048	snp	C/G/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61879472	ATAGATACTGAGTGA[C/G/T]GACTGTATATATGGT	220441
rs376256617	snp	C/T	0.0788843	0.182262	intron-variant	RNF152	GRCh38.p7	18:61861189	AAATGTCCTAGGCCA[C/T]CACATCCACTCACCA	220441
rs376289536	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811547	AAAAATACTACCTAC[A/T]TTTTAGTTTGGCATC	220441
rs376314589	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61864036	CCTTACAGCCACAAT[C/G]TGTTTCTACCCATAG	220441
rs376329732	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831782	CATGTTAATTACTTC[A/T]ATTTTAAAAAGTGTC	220441
rs376355231	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61892235	GTTCTCTTTCTGCTG[C/T]CCCCAACAGCCCTCC	220441
rs376461385	in-del	-/CTAA			intron-variant	RNF152	GRCh38.p7	18:61833305	AAAATAATTCTCTAA[-/CTAA]TACTCTCAAGTTATT	220441
rs376468175	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61873005	CAAAATTTTGAAAGA[C/T]TAATATATTTTAATG	220441
rs376584971	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61880913	TCTCTCTCTAGTTTT[-/C]TTTTTTTTTTTTTTT	220441
rs376625654	snp	A/G	4.94849e-05	0.00497393	missense	RNF152	GRCh38.p7	18:61816198	AGTTTGATGAAGACC[A/G]GGGTGTGTTCGGAAG	220441
rs376679052	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815559	AATATGTCTATCTTG[C/T]AACATGATTTTGAAA	220441
rs376688755	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61868273	CCAATATTTCTCTTT[-/T]CCTCCTAGCTTATTC	220441
rs376779683	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879880	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	220441
rs376804933	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875883	CCCACCTTCGTCCCT[C/T]CCTGCCCCAATCCAT	220441
rs376806085	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61858639	GCCAGTCCGCAGTAC[C/T]CATTCCTAGGTCTGG	220441
rs376816692	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887075	AACATTTTGGGCAAC[A/G]GTGGATTAACCATCC	220441
rs376820136	snp	C/T	0.000399281	0.0141238	intron-variant, splice-donor-variant	RNF152	GRCh38.p7	18:61867996	AATCAATTTTGCTCA[C/T]CTTCTTAGAACTTAA	220441
rs376936529	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61887722	AAAAAAAAAAAAAAA[-/G]AATGCTCCCTATTTC	220441
rs376939817	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61873233	AATGCTTAAAAGTTA[A/G]TTATTGCCAAGTATA	220441
rs376963124	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818188	AGCACTTTGGGAGGC[C/T]GAGGAGGGGGAATCG	220441
rs376971864	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61842489	GCTTTGTTTCCCTGG[A/C]GACTTGTTTTCACAA	220441
rs376990512	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61821064	TGCTCTGCACTGAGG[C/T]ACATATCTGCCCAGA	220441
rs377034805	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61843868	GAAAAGAGTTACGAA[A/G]ATGGATGGAAGTTAT	220441
rs377151165	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61847953	ATTGCAAGCTCTCAC[A/C]ACACTCACGCTTCCC	220441
rs377278409	snp	C/T	1.65132e-05	0.00287339	missense	RNF152	GRCh38.p7	18:61816105	CTCCCGGGCAGCAGG[C/T]GGCAGCCCATGTCTC	220441
rs377294127	snp	A/G	1.8712e-05	0.0030587	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816513	GAAGGGGAAGGAGCT[A/G]CTTCTCAGAGGCCAC	220441
rs377323993	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881881	CTTGTTAATTAACAG[A/T]CTTCTTATAGGACAG	220441
rs377334730	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846898	TAGTCTGGATTTGAG[C/T]CCCAACTCTTGTCAC	220441
rs377354516	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811016	GAACTTCTATCTTCC[C/T]ATTAAGGCTAAAGAA	220441
rs377355662	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61853898	TGGGGTCCATTATTC[A/G]CCACAGAGTAAGGCA	220441
rs377407224	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879897	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	220441
rs377420728	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61855482	ACCCCCTTTGGGGCT[C/T]TGCAATTCCTCGCAT	220441
rs377488051	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854529	TCCATAGTTTCTTCC[C/T]CTCTTCCTCTTTCTC	220441
rs377551204	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829044	CACAGAGACCAAGAC[A/G]AGGGGAGGCAGTGCC	220441
rs377709960	snp	A/G	0.000153988	0.00877328	missense	RNF152	GRCh38.p7	18:61816291	CCGGGAGGCAGCTTG[A/G]TGACACCGCGGCACC	220441
rs377726310	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61882345	AAAATTCCCCTTCCA[A/G]AAACAAGTCATTTGC	220441
rs377731042	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61815035	AGGTAAATCAAATTA[A/G]ACACACACACATACA	220441
rs377737178	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868174	TACCCACTGTAGAGG[C/T]TGGCCTTCGGGTGTT	220441
rs386387915	in-del	-/AA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809876	AAAAAAAAAAAAAAA[-/AA]AGTCATTGGCTCGAC	220441
rs386803999	in-del	GAG/T			intron-variant	RNF152	GRCh38.p7	18:61829502	GAGAGAGGGGAGAGA[GAG/T]ATATATATATATCAG	220441
rs386804000	multinucleotide-polymorphism	GAGAGAG/TATATAT			intron-variant	RNF152	GRCh38.p7	18:61829506	GAGGGGAGAGAGAGA[GAGAGAG/TATATAT]ATATCAGGGGAGGGA	220441
rs386804001	multinucleotide-polymorphism	CA/GG			intron-variant	RNF152	GRCh38.p7	18:61830170	GGGACTACAGGCACA[CA/GG]CCACTGTAGTCTGGC	220441
rs386804002	multinucleotide-polymorphism	CA/TG			intron-variant	RNF152	GRCh38.p7	18:61833076	CTTCCATTCCTCAGC[CA/TG]TATCTACTAAAATTC	220441
rs386804003	multinucleotide-polymorphism	AT/GC			intron-variant	RNF152	GRCh38.p7	18:61872541	CCAAATATTCATGAA[AT/GC]CATGCCCCTCTCCCA	220441
rs386804004	multinucleotide-polymorphism	CA/GG			intron-variant	RNF152	GRCh38.p7	18:61874476	ATTCAAAATAATGTG[CA/GG]ACTATTTTAAAAAGC	220441
rs386804005	multinucleotide-polymorphism	GTT/TTC			intron-variant	RNF152	GRCh38.p7	18:61885887	ATCAATGCCTGCTCC[GTT/TTC]AGATTGTGGGGTGGT	220441
rs397709630	in-del	-/A	0	0	intron-variant	RNF152	GRCh38.p7	18:61868724	AAAAATAAAAAAAAA[-/A]TAAGTACAGGTTTTA	220441
rs397711787	in-del	-/GG/GT/GTGTGTGG			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810294	TGTGTGTGTGTGTGT[-/GG/GT/GTGTGTGG]AGTAAGTCAGTTGTG	220441
rs397732238	in-del	-/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61866456	ACATCCACACTCTCG[-/G]CCCGCGTTTCTGTGC	220441
rs397767126	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61826570	ATATAAACTTTTTTT[-/T]CCTCTTTACATGTTT	220441
rs397808815	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61828636	TGGTTTAGAAAAAAA[-/A]TGTGATAATATTCTC	220441
rs397816186	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811060	GCAAAAAAAAAAAAA[-/A]TTAAATGATTTTTAA	220441
rs397830349	in-del	-/TTTGTTTG			intron-variant	RNF152	GRCh38.p7	18:61885326	TTGTTTGTTTGTTTG[-/TTTGTTTG]AGACAGAGCCTCGGT	220441
rs397858140	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61834684	AAATTAGGCCATTTT[-/T]AAAAAAAATTAAGCA	220441
rs397956442	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61817757	AAAAAAAAAAAAAAA[-/A]GTGTTAGCATCCTGG	220441
rs398033135	in-del	-/A	0	0	intron-variant	RNF152	GRCh38.p7	18:61887411	TGTCAAGGAGCAGAA[-/A]CAGCAATAGTAAGAA	220441
rs398079543	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812863	TAAACCTACAAAAAA[-/A]ATTCTTTAAAGCAAT	220441
rs398079544	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61868723	TAAAAATAAAAAAAA[-/A]ATAAGTACAGGTTTT	220441
rs398079545	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61887410	CTGTCAAGGAGCAGA[-/A]ACAGCAATAGTAAGA	220441
rs398100920	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61866909	ACAACACAAAAAAAA[-/A]CAGACTTAGGGGCTT	220441
rs398100921	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61884457	TACAAAAAAAAAAAA[-/AA]GCAGAAAACCAAATT	220441
rs398120546	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61836737	AATTTAAAAAAAAAA[-/A]TCCTTGACTCCATAG	220441
rs527297625	in-del	-/A	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61844625	TAAGCTTCCTTTTTG[-/A]AATCACTAGCACAAA	220441
rs527297698	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61826226	CTTACCTGACCAAAA[A/G]CAGAAACTTCTCAGA	220441
rs527300830	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844092	GGAAAGAAAGAAAGA[A/C]AGAAAGAAAGAAAGA	220441
rs527348465	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811248	ATAAAGGGATGGGAA[C/T]TCTTAAAATCAAAAT	220441
rs527350768	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896146	CCATGTTTTAGAAGC[C/G]TAAGGTAATCCTGAA	220441
rs527371168	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61835001	AATTGAGGGTTGAGA[A/G]TCACTGATAATTTCT	220441
rs527380422	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61857081	TATAATTAAAATACA[C/G]GCAGGGGAACAGGCA	220441
rs527401837	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811819	CATGCATAGCTTGCA[A/G]GTCAAACGTTTTACA	220441
rs527472387	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880574	CGTCTAATAAACACT[A/G]TCTACTACTATATTT	220441
rs527514883	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61869805	ATCTTCATAAACTCA[A/G]ACAAGCCACTTACCC	220441
rs527516734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831635	AAAATAAGCAATTTA[A/G]AACACAATGCTCACT	220441
rs527520728	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61878247	GAGACATCTTTGATT[A/G]AACTGGGACAACTGA	220441
rs527538053	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881778	AGAGGGTTTAGCATC[C/T]CCACGCACAAGTTCT	220441
rs527541730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889409	ATGCCGTTATCACAA[C/T]GTGAACAAAGATATA	220441
rs527610344	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882135	ATTTTGGATTTTGGA[C/T]TTTCAGATGTGGAAT	220441
rs527617841	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830906	CTCTGAATCTTGAGA[C/T]TTTGTACCTAGCAAA	220441
rs527667151	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880830	ATTTTGAAAATACCA[C/T]ACACCTACACAATTC	220441
rs527719281	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868112	CTTTTCCTGGCTCCT[C/T]TCTCCAGTCATTTTC	220441
rs527736990	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887331	AGCAAGACCATTGTC[A/G]TAGCCCAGAGAGAAA	220441
rs527760302	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61865047	GAGTTTATGATGAAA[A/C]ACAAAAGATATTCCT	220441
rs527795350	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837650	CTTGCTCAGTTGTTC[C/T]TTTTATTTCTAAGAT	220441
rs527846481	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61862654	CTCCACACCCTGTCC[C/T]CCACCCCTCACCCCA	220441
rs527859652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817477	GCCCTTTCTATGAGT[A/G]GGTTCTGCATCTGCG	220441
rs527927635	in-del	-/AAG	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61892472	TCTATTACTACAGAT[-/AAG]AAAGCAGGCATCTAT	220441
rs527935539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863200	CAGCATTTGGAAGGC[C/T]GAGGCAGGTGGATCA	220441
rs527968762	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61819758	AGGCACAGTGGCTCA[C/T]GCCTGTAATCTCAGC	220441
rs528004121	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822541	CAAAGATCTCCAACA[C/T]TGAATTTTTATAATC	220441
rs528019602	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61823591	GGCGTGAGCCACCAC[A/G]CCCAGCCTTTTGGTT	220441
rs528066740	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61871103	TTCACACCATTGGCT[A/C]CTACAACCTCTCGGA	220441
rs528067501	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61835905	TATTGTCAGAAAACA[A/C]GGCCAAGGCTTTCTC	220441
rs528072152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877819	CTGGCACGGCTGCTT[C/T]AGCAAAGTCTCTTCA	220441
rs528141346	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61847073	ACATAGTAGCTGCTC[A/T]GCAAACACCGGTACT	220441
rs528185680	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895390	CCCACTGCTGGAGTG[A/G]AGCCGTCTTTGTCTT	220441
rs528194324	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877240	AGACACAATGACAAA[C/T]ACAATTGATTGCAGC	220441
rs528210785	snp	C/T			downstream-variant-500B	RNF152	GRCh38.p7	18:61807737	AAGTTGTTCTGTATA[C/T]GGTGCAACAAGTTGT	220441
rs528249210	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859701	CTGGCCAACATGGCG[A/C]AATCCCATCTCTACT	220441
rs528249719	snp	C/T	0.00358779	0.0422022	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814989	ATGAAGTCTTCATCC[C/T]AGGATTCTTCAGCAA	220441
rs528320556	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820256	ATGGTGTGAACCCAG[A/G]GGGCGGAGCTTGCAA	220441
rs528335662	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860208	CCATGCCTGTGGACT[A/T]CCAGCCTCCAAAAAT	220441
rs528374044	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873492	ACAGGCACGCCACCA[A/C/T]GCCTGGCTAATTTTG	220441
rs528389072	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61876456	GTACACTCAGCCCAC[-/A]AAAAAAAATAAGCAA	220441
rs528413837	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865880	TAGTTTGCAAGGAAG[G/T]CTAGTCAGCTGAGTG	220441
rs528424475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864475	GACCTCTTGGGAGGC[A/G]TCACCCTCCCCCAGC	220441
rs528440506	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857791	CATCTTTCAGCCTCA[G/T]TCCTGTTAATCAATA	220441
rs528472964	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814580	GAACTGGTCCACTTA[C/T]ATTGGGAATTTGAGC	220441
rs528517712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858301	CCTGCCAGCCCCTCC[C/T]TCCCCCAAGCCCTCT	220441
rs528529737	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825033	GAAATAACTGACAAA[C/T]CAAGCACACAGGGAA	220441
rs528582308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870361	AATCTTCATGTCTGA[C/T]GCATTTCCTGTCCTC	220441
rs528585925	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827807	TCAGTCTGCTCATTA[C/T]TTCTGCTTTTTCTTA	220441
rs528636066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818828	TGTGTCAAGCGTGAT[A/G]TTCCTTTTTGTCCCT	220441
rs528657035	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890833	ATGTAAGGACCGAAC[A/T]GTATGGAATTCAGCT	220441
rs528657275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882904	ATGCATACAACATAG[A/G]AATGTTCCAGAGGCA	220441
rs528665913	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61870163	TTTATCACGAATACC[C/G]TGCTTTTAGGATTAT	220441
rs528706013	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845956	ACTCAGCCCTCCTGA[C/G]TGGGGTTAGTGCCCC	220441
rs528706338	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839368	AACGTTCACAGTTTT[A/G]AAGATTTCCAGAAGT	220441
rs528759279	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813476	AATCTACCATACAGC[C/T]GATTAATTTTGCACT	220441
rs528765669	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852143	AAACCGTGGCTTCTG[A/G]AAACAGTGGTTCCAA	220441
rs528792776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890267	AGTCACTAGTGCTAC[C/T]CACCCATATCCACTT	220441
rs528860933	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61883436	ATTCCTAAATAAAGG[A/G]GTTGACAAGGCTACA	220441
rs528900089	in-del	-/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61883793	AGACTCAGGTTGCCT[-/G]GGGGCTAGCTCAGAA	220441
rs528929062	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61870471	CGCCTGTCACCTTAC[C/T]TACTAGCTTGCTGTC	220441
rs528993792	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845161	CCTGATCATAGCTCA[C/T]TGCAGCCTTAAACTC	220441
rs529013180	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839301	TTTACTTGTCATAAT[C/G]CTTTAGTCTTCCTCA	220441
rs529037706	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865196	GCAGCCAAATTGTCC[A/G]GCACATATACTTGGA	220441
rs529054352	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61842438	ATTGCTGGAACAAGG[C/T]TGGCAGCTGTCACAC	220441
rs529110177	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825947	ATTTTCCCATTATAT[G/T]TTATCTATGTCAGGG	220441
rs529211316	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869771	CACGCACACACATGC[A/C]CACACCCGGAAGCTT	220441
rs529220499	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61871002	TGGCACCCCAAGGCC[C/T]TGCACCTGCTTCCCA	220441
rs529225305	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870999	TAATGGCACCCCAAG[A/G]CCCTGCACCTGCTTC	220441
rs529306096	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869909	AAGCAGATGTACTTT[A/G]GACAGGAAACCATGA	220441
rs529308193	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818095	TCCCCCATCATGATA[C/T]ATAATGTGTTAACAA	220441
rs529369927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869303	CTTCCAATCATACTT[C/T]CAAGCAACTCAAGTG	220441
rs529399642	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830816	AGCTGGATGGAGGAA[C/G]CATTTTTGAGGGGTA	220441
rs529434840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884006	TGCCATCACCTCCTT[A/G]GCTAGCTTAAGGGCT	220441
rs529437853	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831595	TCCAAGACTACGCAC[A/G]AAGTATTTAAGATGT	220441
rs529462337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858194	CCAGGTCCCACTGAC[C/T]GTGGGCTCGGCTGTG	220441
rs529481128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889635	TCTACTAGTCCTGTG[A/G]CCAGAAAAAGCCTCT	220441
rs529523775	snp	A/C			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892647	ATTTGCAATTTATTT[A/C]TTTGAACCAGGAGTT	220441
rs529548157	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857658	AAAAGTAGCAGATAA[A/C]ACAAGTTCCATATCC	220441
rs529602096	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867090	TCGCCAGCTGAAGTA[C/G]GAAGAAAGCCTGTGG	220441
rs529638296	snp	C/T	3.30147e-05	0.00406279	missense	RNF152	GRCh38.p7	18:61815877	GATATCACAGTGAAG[C/T]GCTTAGAAATGCAAG	220441
rs529714042	in-del	-/A	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61851090	ATATCCACAATGATT[-/A]AAAAAAAAAAAAAAA	220441
rs529759491	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873118	GCTACTAAAGTTCAC[C/T]GTGCTTTCTGTCTGC	220441
rs529772654	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828315	ACTATTCACAAGCAT[G/T]ATCATAGCTCATTGC	220441
rs529774034	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61876954	ACTTGACCATTGTAT[A/C]CTCAAGCCAGATTTG	220441
rs529795578	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828658	AATATTCTCAGTGTA[C/T]TTTAGTGTGTTTTTA	220441
rs529834968	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894475	CCAAAGGGGGTGGGG[A/G]GAGAGGCTGGGCTCC	220441
rs529926645	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841959	ATACGTAACAAATGG[A/C]CATGACTGTGTTCCA	220441
rs529926906	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849021	AGGGGAGCCTGGAGA[C/G]GGCCTTCGAGCATTC	220441
rs529930146	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61829649	GGGGAGTGAAGAGGG[G/T]AGGACCAGGAGGTGA	220441
rs529968384	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830911	AATCTTGAGATTTTG[C/T]ACCTAGCAAAGTCCT	220441
rs529984469	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855158	AGGACAGCAAGATTC[C/T]CCAGTATCTAAGAAA	220441
rs530005111	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809747	AGTATGAATAATATA[A/T]AAAACCTTAGATTAG	220441
rs530011978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853728	TTTTCATAAAAACCC[C/T]TGTGATTACATTGGG	220441
rs530042949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846978	CTTCATGTGTAACTC[A/G]GGGACAATCACACCT	220441
rs530088494	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808102	TTTAATCATAGCAAA[C/T]GTGTTTTTACGGTAG	220441
rs530105731	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814414	CTTCATGAATTCCAT[A/C]AAAGAAGTTAGATGA	220441
rs530108472	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891932	CCCATTTCCATAACC[A/G]TTCTTATTCCCTGCT	220441
rs530213037	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61818503	CACTGTTAAAAACTA[G/T]TAACAATGAAAAGAT	220441
rs530268160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833375	ACATTAGAAAGAAGG[C/T]GGAGGTAGCAAAGCC	220441
rs530306419	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884204	TCTTACACTAACTCA[A/G]TGAGGTCGGTTCTCC	220441
rs530342883	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859250	TTTTGTCCTTCCCAC[A/G]GGTACCATCAAAGCC	220441
rs530346175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878114	GCATCTCATTTCCAT[A/G]TACATCCCATTGGTG	220441
rs530370675	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892724	GAAACCACCCAAACA[A/G]CCCTGTGCCAGCACT	220441
rs530386698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866024	ATTTCTCTCAGGTCT[A/G]TTCCTCCCACTGCCT	220441
rs530442791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885600	GGCGTGAGCCACCAC[A/G]CCCAGCCGAGAGCGT	220441
rs530444625	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820801	TGGGAAGTAGCTCAG[C/G]AGAGTGGGAAGACTG	220441
rs530544278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878722	ACCTTATTGTTGTGT[C/T]CTCACGTGGCAGAAG	220441
rs530571955	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860822	ACAAGATGTGGAGGT[A/G]GAAGGCAGTAATATT	220441
rs530607570	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61893003	CAGACGGGGCTGGAG[C/T]GGGTGCACTAGGGAG	220441
rs530614209	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833860	ATTATAGCTACTTTC[A/G]TAACCTGGTTGCCAT	220441
rs530651350	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827345	AAAATACTAAAGAAC[A/C]TGTATGATTTCAGAC	220441
rs530658292	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61847767	CACTTCCCAAACCTG[C/T]TCTACCCACAGTCTT	220441
rs530678945	snp	C/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61836461	TAAGGCCCTAAGATG[C/G]GATTAGTGCCCTTAT	220441
rs530725369	in-del	-/CAAA			intron-variant	RNF152	GRCh38.p7	18:61857722	AAACAAACAAACAAA[-/CAAA]AACTGTGGGCTTTTG	220441
rs530735230	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61852449	TATTTCCTGCCACAA[C/T]TACAGCATCGCTCAT	220441
rs530849511	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860287	CTAGAAAACTCATCT[A/G]AGGGGGAAGCAAGCA	220441
rs530853665	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61828080	TACAGTTCAACCAGT[G/T]TTGACAAATGTACTC	220441
rs530870205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819450	TATTGGGAGGCTATT[A/G]CATTAGGCAAGAGTT	220441
rs530882930	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815695	AGACCGCACCTTCTG[C/T]CCTTTGTGTCTGTCT	220441
rs530883167	snp	G/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61850311	CCTTGACATATCATC[G/T]GGCACAGAATAACTC	220441
rs530927360	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858400	AGATTCCTGCCAGCC[A/C]TTCCCTCCCCCAAGC	220441
rs530980208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839818	GAGAATGGCATGAAC[C/T]CGGGAGGCAGAGCTT	220441
rs530985689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826413	AACATTCTTATCTCC[C/T]GTTTGAACTCCTAAA	220441
rs531004676	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61843549	AAACATGGGAAAATA[C/T]CCAAATGCCCACAGA	220441
rs531080276	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61870698	TCCTATTTTCCTACT[A/G]TGGTTTATGGACCTC	220441
rs531082829	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61820105	GAGGCTGAGGCAGGC[A/G]GATCACGAGGTCAGG	220441
rs531174412	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61855816	CAGGTACGAGCAATA[A/C]CCAGGCAGAAGGTGC	220441
rs531238915	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61881595	ATGAAATCAAATGAA[C/T]GCTGAAGCAACTAGA	220441
rs531250449	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61891911	TCCTACAAGAAAAAT[C/T]GAAAGCCCATTTCCA	220441
rs531291452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862552	AAGCTTCGGTAAAAA[A/G]ACCCAAGCGGACAGG	220441
rs531292248	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855836	GCAGAAGGTGCCATT[G/T]GCCACAGAGGTTTCC	220441
rs531351584	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817389	TAAAAGCAAGTACGA[C/T]TGACCCATGAACAAC	220441
rs531371198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843940	TATACTTAAAAATGA[C/T]AGAAATGCTCAATTT	220441
rs531395197	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816705	TCTTGACACTGGGCC[A/T]AAAGCCTAAAAATTT	220441
rs531436565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875199	GGGTAACACCTGGAG[A/G]CTAATGAGTTAACCA	220441
rs531522052	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888812	AAAGAAGCAGGAAAA[C/T]CAACACCTTCTTCCT	220441
rs531581735	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61887260	ATTAATTGGCCTAAT[A/G]GTCTAAGAGTGACAG	220441
rs531628746	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815619	GATTATGAGGATGCA[C/T]GCAATCATCTTCCAA	220441
rs531649664	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61881201	TTAGGTGTGATCCAC[C/T]GCACCCGGCCTTCTC	220441
rs531664948	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836638	CTATGAGAAATAAAT[G/T]CTTGTTCAACCCACC	220441
rs531691842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887000	ATAGGATAGAGGCAG[A/G]GGAAGGAAGAGGACA	220441
rs531710247	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61862394	CCATCCTGAAAAGAA[C/G]TTCAGCTGACAAAGC	220441
rs531715295	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879563	GAAAGCGTGTTCCGG[A/G]GAAAGGGAACTACAC	220441
rs531737362	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835205	CTCCACAGTACAAAA[C/T]AGCATATTTACAAGG	220441
rs531774875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873336	CTGCAGTCTCCTTTC[C/T]TTTTGTTTGTTTGTT	220441
rs531808087	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61823104	GCAATCCTTCCAGGA[C/T]ACAACTGCTGCATAC	220441
rs531818739	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848366	GCCACATTTTTTGAA[A/T]GATTCCATAGCCTCA	220441
rs531848141	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886545	CCCCCATTGTAGGCT[A/G]ATTGCAGGTCACAAC	220441
rs531859528	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61868479	TTTGAGAGGCCAAGG[C/T]GGGTGGATTACCCAA	220441
rs531876818	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828907	TGATTGATACTTCAC[A/G]CGGGAGTATCAGGTT	220441
rs531895873	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868012	CTTCTTAGAACTTAA[C/T]GAGCCTCCTAGGGGC	220441
rs531910776	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829502	GAGAGAGGGGAGAGA[G/T]AGATATATATATATC	220441
rs531927166	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61839112	GATTTGATAGTAAGC[-/T]TGCAGGCCTGAGGTC	220441
rs531936838	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861869	CACAGAACATTCATC[C/T]ACTCAAGTGGGATCT	220441
rs531941037	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61817966	CAGAAAAAATTGCTA[C/G]TCCTAGAACCCCACC	220441
rs531967820	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855291	ACCTTAAAAGTTTAA[C/T]AAAATCAGGAAGTTC	220441
rs531980436	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61862028	TGGAAAAATGAATAC[A/C]ACTCCCTGAGGCCCT	220441
rs532022764	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855732	GCTCGCCCTTGGCAG[G/T]TGTGGAATCTGGGCT	220441
rs532094551	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861280	TCCTATACAGGTGTA[A/C/G]CTTTTTTATCTTTTA	220441
rs532122629	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809815	CACCACTACATCATA[A/G]GTGAGATATATATAG	220441
rs532145738	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823027	ACACTCCAATTAGTG[G/T]CAAGAATGGGAATGC	220441
rs532172271	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61849751	TTGGGTTTTCTTTAA[A/G]AGAAGTGGTCTCACT	220441
rs532174647	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880471	GCACAAACTCGCCAC[A/G]TAACCTTGGACAAGT	220441
rs532181792	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61875053	ATGTTGGAGGCAGCA[A/G]AGGCCATTTCCAGTT	220441
rs532209874	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61843216	CTTTTCAACTCGTGC[A/G]CACCCTACAGAAAAG	220441
rs532211383	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811990	CAATGAATTTTTACT[C/G]TCATACTTGAGATCA	220441
rs532221337	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853371	CACAGCTCACTGCAA[C/T]CTCTGCCTCCCAGGT	220441
rs532231883	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61881580	GCCATAGTCAAAGAC[A/G]TGAAATCAAATGAAT	220441
rs532248104	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61830115	CAACCTTCACTTCAC[A/G]GGTTCCAGGGATTCT	220441
rs532297181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842631	TATTAGTCTATTTTT[A/G]CGCTGCTGATAAAGA	220441
rs532373170	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841248	TACAAAGGCCTAAAA[A/T]TCTGGACATTAGAAA	220441
rs532412228	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849169	AGAAACAGGGGAGTA[C/T]TGCCCTGCGGGGGCT	220441
rs532413771	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810417	TTGGGAGGCCGAGGC[A/G]GGTGGATCGCCTGAA	220441
rs532434067	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832748	CCAGCAAATAAAATC[A/G]ACAGGATTTTAAAAG	220441
rs532479805	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884274	TGCACTCAGGTCACG[C/T]GGCAGACGTGAAATT	220441
rs532502434	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847719	TCTCAAAGCTAAGAT[G/T]TCCAAAATGGAATTC	220441
rs532616991	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854410	TGCTAAGACATACAC[A/G]CAGCAACAGCCTTAA	220441
rs532626468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891998	AGAAAATGCTAATGC[C/T]GGAGTGTCCTGCTAA	220441
rs532640311	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809099	GGCCTTCAGCTCCTA[C/T]ATGTCTTGTTTTGCA	220441
rs532656137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834442	TCCTTTTAGTCTCCC[A/G]CACTGAAAAGTGAGT	220441
rs532656263	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841799	CAGTAAATCACTAAT[A/C]CTGCTTTCAGTGGCA	220441
rs532679232	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61862077	CAGAAGAAGCTGGAC[A/G]TTCTAATTCAGGTCC	220441
rs532755747	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844699	GTTTAGGAGAGAATA[A/C]GTGTAACCATAGCAC	220441
rs532766399	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828759	ATTAATGTAGGCACA[G/T]TCAAATGCATATTGA	220441
rs532770551	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867179	AAGAGATTGGGGACC[C/G]GGTGCGGTGGCTCAC	220441
rs532814846	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878971	ATGCAGAATTTTCAC[A/G]CACAGGGTAAGTGGG	220441
rs532815133	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886342	CCCTTCCTGTGTACA[A/G]ACACGGTGGCAAACA	220441
rs532868185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851392	GAGGGGAGGGAGGAC[A/G]GAAAAGAGGAGAAAA	220441
rs532920820	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889535	TTTTAGGGAGAGTGA[A/G]GCAAGGAAGGCTTTA	220441
rs532937289	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61856073	GGTGTCAGGGTTCTC[A/T]TCTGCAAGGGGAGAG	220441
rs532956196	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61882253	TAATCTGCAGAGAAA[C/T]GAACTCTTTGTACTA	220441
rs532971053	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870399	ACGTGGTATTTTCTT[A/G]CTCTGGGCTGTCCCC	220441
rs532985966	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883592	CTGGAGGGTGACCAG[C/T]TCATCCCAATTTTTC	220441
rs532996375	snp	G/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61888921	ACTTGGGTATGAAAT[G/T]AAAGTGGTAGGGACC	220441
rs533006048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864659	TCACAACCCTCTAAT[C/T]ACAGAGTTGGTTCCT	220441
rs533013877	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854501	ACACAGGAAACCATC[C/T]TCTCAATGATTTTCC	220441
rs533020502	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61879844	GTGGCGCACGCCTGT[A/T]ACCCCAGCTACTCAG	220441
rs533027007	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61844122	AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA	220441
rs533163165	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875041	ATGGTCTGCAAGATG[C/T]TGGAGGCAGCAAAGG	220441
rs533225932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882742	GATCTCTAAGATCTC[C/T]GCTATAGGGTGGAGC	220441
rs533250508	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61839849	GCAGTGGGCCGAGAT[C/T]GTGCCTGTGTGCTTT	220441
rs533321285	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61823162	GTCATTGTTTTAATG[C/G]AGCAGGACTTTGACA	220441
rs533351550	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61868665	CCAAGATCACCCATT[A/G]CACTCCTGCCTGGGC	220441
rs533420327	snp	G/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61824364	ATGACCTAAATAATT[G/T]CTGAAAACACTGCTG	220441
rs533452500	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61836548	GAAAGCGGCTCTCTG[A/C]AAACCAGAAAGAAGG	220441
rs533456738	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61825195	GCCATGGTAAACAAG[A/T]GTCCTACCCTCAAGG	220441
rs533516779	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843448	AGCAATTCCACCTCT[A/G]AGTATTTACCCTAAA	220441
rs533520165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863682	CTGTCCTCAACTAGC[A/G]TGCTGTACAAAGTGC	220441
rs533555859	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836790	ACAGAAAAAGAAGGG[C/G]AAAGAAAGGCAGGAA	220441
rs533610045	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857556	AATCTGTTGTTATTG[C/T]TATAATTTTTCTTCA	220441
rs533617899	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61850878	CTCAGGAAGCTCCAT[A/C]CAGGCAGACAGCATG	220441
rs533638542	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817516	ACATCAAAAATACAG[C/T]GTTCTCAGGATGCAA	220441
rs533731864	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862847	GAGGCCCAGACTTAT[A/C]ATTGGTGTGTGGGTA	220441
rs533756277	snp	C/T	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61836153	AAAAAGAAGCTGACA[C/T]CTTTGGAGAAATGGT	220441
rs533812660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874678	AGGATATAAAGCACC[A/G]CCAAGTAGTTTTAAG	220441
rs533820641	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61885371	GGAGTGCAGTGGTGC[A/G]ATCTCAACTCACTGC	220441
rs533823239	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823056	GCCCGGTGACAGATG[C/T]GTCATTGACTTTTTG	220441
rs533839176	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869035	CAGGTTTTTATAAGC[A/G]TTTGAGGTTATCAGA	220441
rs533907771	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888271	GGTCACAGATACACT[A/G]TTTGAGGTCTCCCTC	220441
rs533911889	in-del	-/GT	0.0103295	0.0711199	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813788	TGCAACACTTCTGTG[-/GT]GTGTGTGTGTGTGTG	220441
rs533921496	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880580	ATAAACACTATCTAC[A/T]ACTATATTTCTACTA	220441
rs533947729	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822512	GCGCATTCATTTGGT[A/T]GGTGGTAAAATAGCA	220441
rs533985128	in-del	-/A	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61822225	GGGGAGGGCATTCTT[-/A]AAAAAATAGATGGCT	220441
rs533990835	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61817775	GTTAGCATCCTGGTA[C/T]GGAGGGGAGGCAGAG	220441
rs533993469	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61879755	AATCACCTGAGGTCA[A/G]GAGTTCGAGACCAGC	220441
rs534006486	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824483	ATCTGGCAAGAATGC[A/G]CATTTATGTGAGATG	220441
rs534022132	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61856871	GAGGACTAGCTATAA[A/G]GCTCATCTTCAAAAA	220441
rs534030925	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863112	CCAAAACAAACCAAA[C/T]GTGTTGCCCGTAAAA	220441
rs534032335	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835267	AAAAATCTAAATTCC[C/T]ATCCATAGGAATCTG	220441
rs534042979	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816529	CTTCTCAGAGGCCAC[C/T]GCCCTGTGTCTTTGC	220441
rs534054601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821901	CATCCTGAAACCATC[A/G]GTCCCTACCCATCCG	220441
rs534080591	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61848740	TTTGGAGCCACGGAA[C/G]AGGCCTGCCCGGCAG	220441
rs534090767	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855852	GCCACAGAGGTTTCC[A/G]GCTGGTGACTCCCAG	220441
rs534093738	snp	A/G	0.0248432	0.108648	intron-variant	RNF152	GRCh38.p7	18:61887414	CAAGGAGCAGAAACA[A/G]CAATAGTAAGAAGAA	220441
rs534174830	snp	A/G	3.30273e-05	0.00406356	missense	RNF152	GRCh38.p7	18:61816333	ACATCCTTCTGGCTG[A/G]TCCTCATCTGCTGCA	220441
rs534293842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873407	CAATGGCGCTATCTC[A/G]GCTCACCGCAACCTC	220441
rs534329402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819557	AGGATCTTGCAGGGT[A/G]TTGCAATGAGGTTGT	220441
rs534369537	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871515	TTACTTAGGATCACA[A/G]GGCTGATAATAAACA	220441
rs534387895	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891872	AGAGTAGACCAGGAG[C/T]CTTTGGCCCTCAGCA	220441
rs534469456	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61845733	GTAGCAGAGGCAGCC[C/T]GAATAATAGTACTCC	220441
rs534548131	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF152, LOC105372159	GRCh38.p7	18:61894251	TTTCAGCCAGACTCG[C/T]GCCCCGGGCCGGCGG	220441
rs534556704	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813929	ATAGTATTCAGCTAA[C/T]ATGACACCTAAATTA	220441
rs534591477	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864736	GTCATCTCATTAGCA[C/T]AAGCCAAGGTATGGT	220441
rs534598681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842517	CAAAAGTTAGGACCT[A/G]CAAGAGACTCTTCTC	220441
rs534630992	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61852410	CTGAACATACTCAAG[A/G]GTGTTGGGTAATAAA	220441
rs534638698	snp	C/G	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814610	CTGTTAGTTTACCTT[C/G]CCACCTTTCTTGGTA	220441
rs534662060	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61850959	CATGTTTGCTTTCAT[A/G]CATGATTGGCTGTGT	220441
rs534674134	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61876907	ATATTTGGAAGTTAA[A/G]ACACCTAGCAGGATA	220441
rs534718719	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61870521	ACCCCTGCCGACTCT[C/G]TGGTTCCAAAGCCTG	220441
rs534726926	snp	G/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61869298	GTCTTCTTCCAATCA[G/T]ACTTCCAAGCAACTC	220441
rs534753592	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61826019	GCTTCTAGGCTTTGC[A/G]GATCCTACAGTCTCT	220441
rs534820802	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891446	CTATTAAAAAAAAAA[C/T]CACACCCTTGTTTCT	220441
rs534824678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857233	GACACTTTTCTATTT[C/T]GCAGATGAGAAAACT	220441
rs534857338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846208	TCATAATTCTCAACC[C/T]AAACACTCTCTCTTG	220441
rs534903129	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876290	TCCCTTTGTACGCAT[G/T]TTCTTACTCCTGCAG	220441
rs534938352	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61824002	TTACCCAGCCCCAGG[G/T]GCATTTTGTTTATGT	220441
rs534942878	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61834636	CTCAGTAAGTGCTCA[A/G]TAAATGCTTGTAGAA	220441
rs534953317	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61849877	CTGACATCATCAAAT[A/G]AGTTTGAGGAGCACC	220441
rs534957874	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881956	GTTATAAGATGTAGG[C/G/T]TGTATGAACAATTAA	220441
rs534958658	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813899	CCAACAGTATATTAT[A/G]TTATGTAATAGAGGA	220441
rs535020176	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882441	TATCTTGGTGTGCAT[A/G]ATGATTACATGGGAA	220441
rs535070120	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811595	ATATGCCCACACCAA[A/C]TACAACGACAAGCTG	220441
rs535098640	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825210	AGTCCTACCCTCAAG[C/G]AGCCTGGATGTACAA	220441
rs535193393	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61838510	GAACCAAGATTCAAT[G/T]AAATGGACCTCAGTG	220441
rs535195125	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831240	CACCACTGTCGCTAG[A/T]CCACAGCCACTTCTC	220441
rs535202192	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824653	CAAGTCTGATCAGTA[A/G]CCTTCCCAGATGAAG	220441
rs535226256	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61868270	GTCCCAATATTTCTC[-/T]TTTCCTCCTAGCTTA	220441
rs535299377	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875265	AATATTCCAGACAGG[A/G]TCCTATATGGAACAG	220441
rs535310181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852362	TGGCTGATTGAAAAT[A/G]TGTTTGCCACCAGGA	220441
rs535313451	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844894	AAAAGCATTTATTCA[C/T]CTACTCGCCCCAGTG	220441
rs535320685	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61818949	GTACCCTAAGGGAGC[C/T]GAAGGAATCAGGGGG	220441
rs535337216	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61845990	TAAAATAAGTCCAAG[G/T]GAGCTCACTTATCTC	220441
rs535337385	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863952	CTTTTCCATGTATTT[C/T]AATCTTTCTCTTTCT	220441
rs535404229	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61857931	CAATAACAACAGGAG[A/C]AAAAAACAACTCTAG	220441
rs535439993	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870039	AGACAGGCAAGTCAC[C/T]ATATAACTTGTTATA	220441
rs535444925	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856667	TTACTAGAGGTGAGG[C/G]GTTGGGGGAGGGGTG	220441
rs535461354	snp	A/G	0.000399281	0.0141238	intron-variant	LOC105372159	GRCh38.p7	18:61896424	TTTTGTAGAGATAGG[A/G]GTCTCTCTTTGTTGC	220441
rs535499156	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875470	GTTCCTACAACCCTT[C/T]AGACCTATGCCTTTA	220441
rs535531702	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61838413	ACCAGAGACGGAGGA[A/G]TCATACTTACATCCT	220441
rs535538380	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61889775	TGCAGGAGGCCACCT[A/C]CTGGGTGGCCCTAGG	220441
rs535538528	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61857203	TCCCCAACACTGTAA[C/T]AGGGAGAAAGTGCAG	220441
rs535592994	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61820444	AATACAGGGTTCGTT[A/G]GTGAATCCTGCTCTA	220441
rs535607240	snp	A/C	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61817630	GTATACATGGGGGTC[A/C]TGGAACCAATGCCCT	220441
rs535681001	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837468	GGAAGTATTCCAGGG[G/T]AAAACGTCATGATGT	220441
rs535801714	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61889024	TTTCATTTTCCTTCT[A/C]CCTCAGTCTGTGCCT	220441
rs535834881	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841585	ATTCTTAACTTTGGG[A/G]GGTTACAAGTCATTC	220441
rs535851378	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61892312	CAAACACTATTACAA[C/T]GAAGGAACAGAAGAA	220441
rs535860763	snp	C/T	0.00517822	0.0506191	intron-variant	RNF152	GRCh38.p7	18:61841268	GACATTAGAAAGCTT[C/T]CACTTTATCAAGGTG	220441
rs535894955	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61850278	TCTGGCTGATAAAAT[A/G]AGAAATGTGTGCAAA	220441
rs535907160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823859	CTGGCTGCAGCCTAG[A/G]TGCTGTCCCTGTCTG	220441
rs535914041	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854608	TAGTCATCTTTTGAA[C/T]GAGGTATTATTTAAG	220441
rs535921946	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814718	GGAAGAGCATCTTTC[A/C]AAAAAGAATCACAGG	220441
rs535932273	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61868791	AATGAAAAGCATAAA[G/T]CAGTAGTGTGCCTTG	220441
rs536027550	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61844205	GAAGGGAAGGAGGGA[A/G]GGAAGGAGGGAGGGA	220441
rs536105242	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812077	GCCCACAAACTCTCA[C/T]CTTAGCCTCACTGTT	220441
rs536113882	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61893025	ACTAGGGAGGTGGAG[A/C]AAGGCAGATGAGGTG	220441
rs536127090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885058	CTCTTTACCTGCATG[A/G]TTGAATTAACTATTA	220441
rs536128630	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61843551	ACATGGGAAAATACC[C/T]AAATGCCCACAGACA	220441
rs536137661	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850922	CTAGTGCAGCTCTGG[A/G]CACACGGAAATGCCC	220441
rs536148794	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871978	GAAACACTTAAGACT[A/G]GGTAATTTATAAAGA	220441
rs536214403	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846101	CTTGGACTTCCCAGC[C/T]TCCAGAACTGTGAGT	220441
rs536225656	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61839538	CGTCCTAGCAGGTGG[C/T]TGTGTTGTAGTAACT	220441
rs536307283	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61820963	GGCTGAAGGTCAAGT[A/G]AGCTCATGGGATCCA	220441
rs536442390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872014	GGCTTAATTGGCTCA[C/T]GGTTCTGCAGGCTGT	220441
rs536537221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847926	AGGTCTTCCTTGACT[A/G]CCTTTTTACACATTG	220441
rs536642145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884053	TGCCTATTCATCCCG[A/G]TATTTCCAGAACTGA	220441
rs536713954	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61877798	TTTTACTCACTACCA[C/G]GAATACTGGCACGGC	220441
rs536718946	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61871729	CAGCCTGGCTTGTTC[A/C/T]GGTAGGGACAACTCA	220441
rs536743959	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61819811	GGATCACTTGAGGCC[A/G]GGAGTTTGAGACCAG	220441
rs536777265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891150	ATGAATAAATGAGCA[C/T]TGTAGAAAGGAAGCA	220441
rs536858174	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61827379	TAGAACTTCATTAAT[C/T]TGAGGTACCCTAAGG	220441
rs536905026	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807720	TTCACAGGGGCTGCA[A/T]GAAGTTGTTCTGTAT	220441
rs536921800	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61856247	CAATGTCAAAGACTC[C/T]TGAAAACTAAATGCT	220441
rs536931092	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61846464	TGCTGCCAAGAGTTT[C/T]TTCTCTACCTCCCTG	220441
rs536966629	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809425	CATGCTCTTCCACCA[A/C]TATTATATCCAACTG	220441
rs537000621	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852208	AACTGGAAACATAAG[G/T]ACATAAGACAGAAGT	220441
rs537071999	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814671	TCATATCAACAAGAG[A/G]AAACAGGAATTCTAA	220441
rs537091949	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61859810	CTTGAATCCAGGAGG[C/T]GGAGGTTGCAGTGAG	220441
rs537096710	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61824336	CTAAAGCACCTTCTA[C/G]TAAAAATATTCTATG	220441
rs537165401	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858657	TTCCTAGGTCTGGCC[C/T]TGTTCTTACTGAAAT	220441
rs537183046	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820284	CAATGAGCAGAGATC[A/G]CACCACTGCACTCCA	220441
rs537243224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884963	CACCATAGGTGAATG[A/G]ATGGATCTGTACCTT	220441
rs537245935	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870685	AAAAGGATCGAGGTC[C/T]TATTTTCCTACTATG	220441
rs537259557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840628	CTGAGAACTAGTCCT[A/G]CACCTTGCACAATTC	220441
rs537272698	snp	C/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61822640	GATAGTTTTACTCTG[C/T]TTACACTCTTAAGAA	220441
rs537300387	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876428	AGCATTAGCTGACAA[C/T]GAAGTTGAGAAAGTA	220441
rs537300530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883130	AGACTGGTTCAAAGC[C/T]CACAGTGTTCAGCCC	220441
rs537420021	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849182	TACTGCCCTGCGGGG[G/T]CTTCACCAGCTCACA	220441
rs537434456	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887593	TAATCCCAGCTACTC[C/G]AGAGGCTGAGGCAGG	220441
rs537440065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879921	AGTGAGCCGAGATCC[C/T]GCCATTGCACTCCAG	220441
rs537494396	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845458	CAAACTGACTCAGCC[A/T]CCTGGGAGCTTTTGT	220441
rs537531384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848673	TGGAAAGCCCCTACT[A/G]ACCTCAGGGTGGAGG	220441
rs537645536	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833437	TGCCCCACTGCTACA[A/G]CTGCAAATCCAATTC	220441
rs537646884	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812010	ACTTGAGATCACATA[C/T]TTTTTAAGCCCAGAA	220441
rs537704249	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880492	TTGGACAAGTCACCA[A/G]GCTTTTCCAAGTTCC	220441
rs537721682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832420	TAGTCATTTTAGTTA[C/T]AGTAATTAAGTTTCA	220441
rs537727484	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839428	TTGGGTTTGTGTGAT[A/G]TTTTCTCATGAATGG	220441
rs537744543	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836086	GTGACAGTCTAGTAA[A/C]AATGAGCACACTTAG	220441
rs537751571	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882807	TTACAGACTCATCAC[A/G]AAAACCCTCTGGAAT	220441
rs537757475	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874196	AAGGCAAAATGACAT[A/C]ATAATTTCCCCTAAT	220441
rs537758456	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61853681	GTTCTGTCACTATAT[C/T]TCCTACCACTAACTT	220441
rs537814919	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834529	TATTGACCTTTATTT[A/G]CCTTCATCTGCCTCG	220441
rs537816708	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61827779	AAAATTAAGCACTGC[A/G]GGGAGTCAGCTGTCA	220441
rs537819375	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61842126	GGTTCACATGTATTT[C/T]TACCACAAGTTGATC	220441
rs537841554	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61855249	TAAGGATGTCATTGT[A/C]AGAGAATTCTGGTTT	220441
rs537900307	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809970	ACTCGCCCTAACCAC[C/T]TGAGCAGATCCAAAA	220441
rs537904333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885781	GGAGGTAAAACAGAT[A/G]TATATCACAAAGGTA	220441
rs537927986	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859934	TAGTATCTCAGAATG[C/T]AGCCTTATTTGGAAA	220441
rs537928351	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61834081	GAGCAAAAGATGTGA[C/T]CCCTGGGTAGTTGTC	220441
rs537932584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841315	AATATCTCCAGACCC[A/G]CAACATAACATGACA	220441
rs537974518	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61886836	ATCTATGACAAGTGG[C/T]CTTTGTAGAATGAAT	220441
rs538017826	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861406	GTACAGGTTTGCAGC[C/T]TTGGAGCAATGGCTG	220441
rs538057459	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61830296	CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC	220441
rs538099099	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855392	GCAGGGACGCCAGCT[A/G]TAGTGGGGGAGGCGC	220441
rs538188696	snp	A/C	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61822498	GTGTGACAAAGTGCG[A/C]GCATTCATTTGGTAG	220441
rs538208168	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808337	CAACATTTGGACAAT[A/G]TTTTCTACACAGCCC	220441
rs538240329	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872833	TTACTAAAGTACACC[A/G]TGACTGAAATTAAAA	220441
rs538244837	snp	C/G			utr-variant-5-prime	RNF152	GRCh38.p7	18:61816584	GGCATCCAGTACTCA[C/G]AGGTGTGTTCATTTC	220441
rs538265103	snp	C/T	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61888822	GAAAACCAACACCTT[C/T]TTCCTTTCCGGTTTC	220441
rs538272792	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866796	TTCCCCTACTTGCCC[A/G]CTGTCCCCACCGCTG	220441
rs538369441	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61829842	CTCCTATTCTGTAAT[C/T]TGGGTTTTGTCTTGT	220441
rs538463047	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809349	CCACTATTTAACAGA[A/G]GTATCAACTAGATCC	220441
rs538479275	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880402	CTCACAGGCAGTTAA[A/G]AGGAAGGACTCAAGC	220441
rs538495973	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879288	ATCATGTTTACATTA[C/T]ATTTGCATAGCATTT	220441
rs538520688	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61886800	AAAAGACACTTCAAT[C/T]GTAGGTGATAATACA	220441
rs538523334	snp	A/C			missense	RNF152	GRCh38.p7	18:61816351	CTCATCTGCTGCAGG[A/C]ACACTGAACAGCAGG	220441
rs538525659	snp	C/T	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61821885	TGAGGTGGAACAGTT[C/T]CATCCTGAAACCATC	220441
rs538577714	snp	G/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61863208	GGAAGGCCGAGGCAG[G/T]TGGATCAGCAGGTCA	220441
rs538584319	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61847988	TGTGATTATTTTTCT[C/T]CAGATGCAGATCATC	220441
rs538585247	snp	C/T	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61879837	AGGTGTGGTGGCGCA[C/T]GCCTGTAACCCCAGC	220441
rs538613831	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840586	GCTTCATAGATGGAT[A/T]TTCAGAGTCCCTGGG	220441
rs538679457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841537	TCAGACATGAACCCA[C/T]ACTGAGTCAAGGCCA	220441
rs538697654	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808670	GCAAACACAAACAAG[C/T]GGTGAAATGAAAAAA	220441
rs538740924	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854754	AAAGAACCCAGTGCT[A/G]AATCATGGCCACTTC	220441
rs538753069	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893089	GCTCCTAATTGTCTC[C/T]ACAGGATAAATAACC	220441
rs538765945	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61856880	CTATAAAGCTCATCT[C/T]CAAAAAGCCATAATT	220441
rs538786178	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809235	TCTACTTAATAGTTG[C/T]ATTGTCCCTCAACCC	220441
rs538829246	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61829068	CAGTGCCCAGGGTGG[G/T]TACGGGTAGGGACCA	220441
rs538835965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860071	GACTCACAAGGAGAG[A/G]CAGCCATGTGATGAC	220441
rs538836269	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866689	TGTGTGCTCCTACAG[C/T]GACATGTTCATCCCT	220441
rs538874261	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860495	TTGTTGCACTGCAAC[A/G]CATTACTCACATGTT	220441
rs538885451	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821749	CCGCCTGAGCTCCAC[C/G]TCCCGTCAGATCAGC	220441
rs538887758	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854014	GTCCAGGGTTGACTT[G/T]CCCAGGTCCACACCT	220441
rs538913573	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834697	TTTAAAAAAAATTAA[A/G]CATATCTGGCTACCA	220441
rs538949923	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866192	GCCCAGCAAACTAGG[A/T]TCTCCCTGCCTCTCA	220441
rs539013575	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837350	CAAGGCATTTTAAAA[C/T]ATGAACTGCATATTA	220441
rs539022113	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61878176	GAAAGTAGTATAGTC[A/G]AGTGATTGTCAACTA	220441
rs539109643	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61884090	TGATTGGTGGATGGT[A/G]GATGCTGGATATAAG	220441
rs539170457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884814	TCTGCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG	220441
rs539207988	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857343	CACACACTATGTCCA[C/T]ATGATTTTATTTTCA	220441
rs539260784	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815235	GTGAAGAAAATGAAG[A/G]TTCATGACAAAACAC	220441
rs539275684	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857834	AAATTTGTCATTGGC[A/G/T]TGTATAAACATCTAC	220441
rs539349615	snp	G/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61824538	AGAAATTTCTCCCTT[G/T]ATGCCTTCAGCTTAA	220441
rs539360074	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61849495	CCCCCAACAGCCACA[C/T]GAAGGGGATTGAAGT	220441
rs539361793	in-del	-/A	0.328382	0.237395	intron-variant	RNF152	GRCh38.p7	18:61836727	TAAGACACTGAATTT[-/A]AAAAAAAAAATCCTT	220441
rs539384572	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818209	GGGGGAATCGTTTGA[A/G]CTCAGGAGTTTGAGA	220441
rs539416472	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61875293	CAGTCCTTAAGCACC[A/G]TCTGTAAAATCTTTT	220441
rs539417995	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869068	AGATTCTGAGAATAT[G/T]CTAACATCTCAGAGG	220441
rs539428194	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61823927	ACTCTGCTAGGGCAT[A/G]TGCCAATTCTGTCGC	220441
rs539442878	in-del	-/AAG	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61867462	ATCTCAAAAAAAAAA[-/AAG]AGATGACAAACTGAA	220441
rs539470762	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816914	TTTAAGCAAGCTCTG[A/G]GTCATCCTTCTAAAA	220441
rs539491703	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61881264	TTGGGGAAAACAAAA[C/T]GTATTTAGCTGTTAA	220441
rs539503418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824742	CTTGAAAAGAAGCTG[C/T]ACAGTTTTCTGGCTT	220441
rs539513104	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874036	ATTCATGATCATTCT[G/T]CATACTATAATAAGT	220441
rs539529569	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818631	ACTACATAGCTATCC[A/G]CTAATTCAAAAAATA	220441
rs539531995	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61874783	ATCTAATCCCAGTCT[C/G/T]GTTCTTAGCTATTGT	220441
rs539551142	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868131	CCAGTCATTTTCCTC[A/G]TAGCCAGCACAGGCA	220441
rs539581016	snp	C/T	1.6838e-05	0.0029015	missense	RNF152	GRCh38.p7	18:61816406	GCCTGCGCCGGGGGC[C/T]GTAGTAATTGAAACA	220441
rs539583378	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61838304	CAAACAATCCTAATT[C/G]AATTTCAGACTCCTC	220441
rs539601540	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850082	TTTCTCAATCCACCT[A/T]ACTGTGGATTCTACC	220441
rs539608821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863980	TCTGAAAAACACCCA[A/G]TCATTGGACATCAGG	220441
rs539633669	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61888355	GTAACAAGCACAGAC[A/G]GTTCCCTACTTACAA	220441
rs539647993	snp	C/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61851141	GTTGGTGCAAATAAA[C/G]CATTTCAGGTCTTAC	220441
rs539675359	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896067	GTCATCTGACTGATC[C/T]TTATCCCTTTGTTCA	220441
rs539709453	in-del	-/ATAA	0.0283406	0.115616	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810648	GCAAAACTCCATCTC[-/ATAA]ATAAATAAATAAATA	220441
rs539715526	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889140	CTCCCAATTCAGAAA[C/T]GCTTTGGGTGCTACA	220441
rs539755594	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825142	AAGCAGATATTTATT[A/G]TGAACTCACCTTGTG	220441
rs539791142	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811310	AGAATCTGGTCTTTA[C/T]AGGAAATATATCTCA	220441
rs539845032	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881208	TGATCCACCGCACCC[A/G]GCCTTCTCTCTCTCG	220441
rs539868843	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855959	CACATACTTTAATCT[A/G]ACCACGCCATGTTTC	220441
rs539881829	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855564	GTAGAAGCCACGTGC[A/T]GTGCATCTGGTGCAG	220441
rs539913215	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61862632	GCACCCACGGAGGGC[A/G]TAGAAGCTCCACACC	220441
rs539919916	snp	A/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61822608	GGATAAAAAAAGCCA[A/G]TGAAGTAGATAATCC	220441
rs539927454	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61835617	AATAATAAATTAAAA[A/G]GGATAAACAAAATCA	220441
rs539941122	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861686	AGAAGGTTCAAGACT[C/T]GGCATTTGGCGAGGG	220441
rs539976716	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61842862	ATCACAAGAACAGCA[C/T]GGGAAAGACCCGCCC	220441
rs539994095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873681	ACATCTTACAGCAGT[A/G]GGGTTACCACCACCA	220441
rs540048146	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856146	TCTAAAAGCTTCTAA[A/G]AGCTCCATTAACAAA	220441
rs540061475	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895688	TATTTTTGGTAGAGA[G/T]GGGGTTTCGCCATGT	220441
rs540069194	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810920	GAAACAAAATGCTGA[C/G]TGGTGGGCAGCATCA	220441
rs540103506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61868220	CATATATCTGTGTTA[C/T]GTTTCAGGGATGTTT	220441
rs540103645	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861802	GGAGGCAGGCTCTTT[C/G]TAACAACCAGCCCTC	220441
rs540142856	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61849440	CCTGAGCAATTACAA[C/T]GAATAACTACAAAGC	220441
rs540150543	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856517	GGGTCATAGCTAGGA[C/G]CCTTCTAGCCACCAA	220441
rs540164732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887787	TCAATTCTTGTCAAA[C/T]CTCAGTGAGGAGTGC	220441
rs540258297	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847650	AAACTGAAAACTACT[A/G]AACACTGACAACAGT	220441
rs540275296	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873219	GCAGAATTTCACAAA[A/C]TGCTTAAAAGTTAAT	220441
rs540299474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828688	AGAAACAAAGTTTTT[C/T]ATCCAACTTCTTATT	220441
rs540314556	snp	A/T			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814676	TCAACAAGAGGAAAC[A/T]GGAATTCTAACTGGC	220441
rs540464828	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61842210	TACTGAACAATTTGT[C/T]GTGAACAAGCCATTG	220441
rs540520854	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809393	TTTGTCATCTCTATT[C/T]CCTTCTGCTTACAGC	220441
rs540526648	snp	A/G	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61855659	CTGGTGTGCCTGGCT[A/G]TGCACAGTGGCTGGA	220441
rs540529199	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61886582	ATCAGCCAGCCACAG[G/T]CCCCCTTGGAAGGAA	220441
rs540540104	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848269	CTCTCTGACCCACCA[C/T]AACAGCTAAAGTTTT	220441
rs540560121	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817142	GTTCCTCTTCACAGA[A/G]AAGTAAAGTGACACT	220441
rs540649513	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813024	CAAAACGGACTCATC[C/T]ACAAAATGAAGCCAC	220441
rs540655742	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844649	GCACAAACAGGCCAA[C/G]AAATTATTCATCTTG	220441
rs540727762	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61818517	AGTAACAATGAAAAG[A/G]TCAACATACTTTAAA	220441
rs540762569	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812481	TTCTGATCATTAAGT[A/G]TGACTGGAACCAAAA	220441
rs540770463	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857486	GCAAATTTTCAAAAG[C/T]CATAAAAATGGCTTT	220441
rs540773750	in-del	-/AC	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61886459	TTTTTCACTTTCAAT[-/AC]AGTATTCAATAAACT	220441
rs540778946	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839107	TTGAATGATTTGATA[A/G]TAAGCTGCAGGCCTG	220441
rs540818872	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61888182	TCCACGAAGAACGTA[G/T]TCCAGGCCTTAGCAG	220441
rs540845005	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61865628	CTAGCAGCTTCCATC[C/T]CGTTGTGGAATTTAG	220441
rs540865087	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839627	TGGGCTGGGCACGGT[A/G]GCTCACCCCTGTAAT	220441
rs540907460	snp	C/T	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61832588	TCTCAATAACTTATC[C/T]TTCTCAGGATAGTCA	220441
rs540908546	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877069	TGTGCAAATAGAACA[A/G]GCACACAGACCACTG	220441
rs540916209	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893221	AGGTGGGGAATAACA[C/T]CTTGGGGCAAAGACA	220441
rs540975493	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886268	AATTCCTTTAAATCA[C/T]TGTAAGTCAAAATCG	220441
rs541016462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857999	TTGGGTCTCCTCTGC[C/T]ATAATCTATTAAAAT	220441
rs541045906	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851894	TATCATCTTTCTAAC[C/T]TCAACCTAGAAGTCT	220441
rs541092334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863559	TTAATATCTTTGGGG[A/G]AAAAACTAAGCACAT	220441
rs541177545	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61888580	GTAGGCTAATGCGCA[C/T]TTCTGGGCACAGTTA	220441
rs541240264	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824328	ATGGTCCCCTAAAGC[A/C]CCTTCTAGTAAAAAT	220441
rs541294567	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61822595	ATATGAGCCCAAGGA[-/T]TAAAAAAAGCCAGTG	220441
rs541318290	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61889958	TACCTAATGGCCTTT[C/T]ACTTCAGAGTAAACA	220441
rs541333245	in-del	-/GA			intron-variant	RNF152	GRCh38.p7	18:61824992	ATGATCAATTACCCT[-/GA]GACTGCCAGAATTCT	220441
rs541333829	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61843879	CGAAGATGGATGGAA[A/G]TTATGGTTGTACAAC	220441
rs541338257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830687	AGGAAAGAGGGGCAA[A/G]GCTGGAATGAAGGTA	220441
rs541387701	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843590	GCAAAGCAAAATATG[G/T]TATGGCCATACAATG	220441
rs541389680	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836452	TCATGAGGGTAAGGC[C/T]CTAAGATGGGATTAG	220441
rs541447789	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841969	AATGGACATGACTGT[A/G]TTCCAATAAAACTTT	220441
rs541550993	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843181	AACAACTGTTGCTGA[A/G]TGACTGAGAAAACTA	220441
rs541558956	snp	G/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61872857	ATTAAAACTCTAAAA[G/T]TTTTAGTATTTCATT	220441
rs541561996	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61880907	TGTCTTTCTCTCTCT[A/C]GTTTTCTTTTTTTTT	220441
rs541568920	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863162	GTCCCTTAGCCAGGC[A/G]CGGTGGCTCACACCT	220441
rs541615877	in-del	-/AAAC	0.00445135	0.0469666	intron-variant	RNF152	GRCh38.p7	18:61857698	CACCAGTCATTAAAC[-/AAAC]AAACAAACAAACAAA	220441
rs541667294	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882079	AAATCAGAAACTTTT[G/T]GAGTGCAAACATGAC	220441
rs541744843	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61851278	TTAAAATCAAACTTT[A/G]AATCACTGAAGTCCT	220441
rs541822721	snp	A/G	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61848389	TAGCCTCAAAGAGAA[A/G]CTCTAGGTTTATATG	220441
rs541843282	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61857418	TTGCCTTGGAACTGC[A/T]TTAGAACCTTTAGGG	220441
rs541886280	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880299	CCCAAAGACAGGTCC[A/G]CAAAGAATTCAGATC	220441
rs541886968	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853892	CTTCTCTGGGGTCCA[C/T]TATTCACCACAGAGT	220441
rs541911993	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810220	ACAAATTGGAAAACA[C/T]GACTAATAACAGTTT	220441
rs541917361	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869154	TGAGCTAAAGGAAAG[C/T]CCAGTCTTAATCATT	220441
rs541948115	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61863527	GATTCTTCTACTGAC[G/T]TTTTACATGGAAATA	220441
rs541965506	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895435	CCGCAAGGAAAGAGT[C/T]CCCATTTTCACTCCC	220441
rs542027006	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830607	ATATTCAATTGTGTA[A/T]TATTTTTTCTTTTTA	220441
rs542054676	snp	C/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61889884	AGAGAAAGTCTGTAA[C/G]TAACACCTCTCTATT	220441
rs542064044	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812299	CCGTACCAGACGGCA[C/T]AGGTTTTCGAGCATT	220441
rs542120699	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841736	CTCTCCATGAAACCG[C/T]AAGTGAAGAACTGGT	220441
rs542190507	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827205	TAGCAGGCCACAAAG[C/T]AGCTGAATAAATTTC	220441
rs542207597	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849527	ACCTGCCCAAAGTGG[C/T]CACTGAGCTAATGCC	220441
rs542240510	snp	C/T			downstream-variant-500B	RNF152	GRCh38.p7	18:61807700	GCCAAGTCACTCTAC[C/T]CTACTTCACAGGGGC	220441
rs542291461	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61824563	GCTTAATGAGTGCAT[A/C]TAGCTAGAGCCCATA	220441
rs542353504	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887261	TTAATTGGCCTAATG[A/G]TCTAAGAGTGACAGC	220441
rs542366790	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61848957	TCCAGCACAAACCAA[C/T]AGCCCGTGGAGATCC	220441
rs542378547	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853583	AGGCTGAGCCATCGC[A/G]CCTCACCGGTTCCTT	220441
rs542400792	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807769	CTGTATATGGTTCAC[C/T]TGGGACCTGGGGCAT	220441
rs542406790	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883479	ATTTTATTCTGCCCC[A/C/G]CTTGCTCCTCTCTTG	220441
rs542423864	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874946	AAGTAAGATGCTTGA[A/G]ATGCAAAGATGAACA	220441
rs542431757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834135	GGCTTGAATCCCACA[C/T]TCCAGCCACTCTGAG	220441
rs542468364	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61827905	GTACAAACCTTGAAA[A/C]TAGATATGGAACAGC	220441
rs542592380	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870276	CCTCCGCACTCCAAA[A/G]AGAAACAGGCTCTCC	220441
rs542615633	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884323	ACTTTTTAAAATTCC[A/C]GTTCATAATGACTTA	220441
rs542682543	snp	A/C	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61875944	ACACAGCTTTATGAC[A/C]ACATCCTCCTCCAGT	220441
rs542692277	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61840260	ACTGTGAGAAATAAG[A/T]TTCTGTTGTTTATAA	220441
rs542742550	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61831623	TGTAAGATAAAAAAA[A/T]TAAGCAATTTAGAAC	220441
rs542879117	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877768	TGTCCCTTTTTTTGT[A/G]TTTGGAATCTCTATT	220441
rs542880959	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870742	CAGGAAGAAATGAAG[A/T]GAAACCCACATAAGG	220441
rs542920433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864299	CACAACCCCCTCTCC[A/G]GTTTAGTAACTTGTG	220441
rs542955275	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858196	AGGTCCCACTGACTG[G/T]GGGCTCGGCTGTGAC	220441
rs543008480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844997	GCCATAAGTGGACAC[A/G]AGTGCTGAAAACATT	220441
rs543053993	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825579	CAAGAGATGCAAGAT[A/G]TTAAGATGGTAACTT	220441
rs543109828	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813186	AAATGCCAGAAGAGG[C/G]CAGAGCAATGGGATG	220441
rs543183012	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833292	CAGTCTATTTCAGAA[A/G/T]ATAATTCTCTAACTA	220441
rs543188124	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814080	ATCAATTTGAAAAAT[C/G]AGAGCTCACAATTTT	220441
rs543197268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858854	CAAAAACAGAGATCC[C/T]GTTTTAATAGGAGAT	220441
rs543220190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826414	ACATTCTTATCTCCC[A/G]TTTGAACTCCTAAAA	220441
rs543220237	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833712	GCATTTTAAAAATGT[C/T]ATCCATCCCTGAAGC	220441
rs543223177	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840204	TCTTACCAGACACTG[A/G]ATCTGCCAGCACCTT	220441
rs543233842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852567	ATTGTCAGTCTTCAA[A/G]GAGAAACTGATTTAT	220441
rs543334788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819222	ATAAAACTCTCAGAG[A/G]ACCTGCAAGCACTCT	220441
rs543387706	in-del	-/AC	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61892499	ATCTATGGAAACCTA[-/AC]ATTCAGATACAACTG	220441
rs543403264	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875722	TGTGTATGTCTCACC[A/G]CTCATTCAATTAATC	220441
rs543412532	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890773	CATAGGTGGGTTCAA[A/G]CAACTCTGAGGGAAT	220441
rs543448744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882778	CTGGTTCCCTTCCCA[A/G]CCCCCACTTGGTATT	220441
rs543483616	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61819423	TTCATTCAAGGGTAG[A/C]CTGGAAAGACCTATT	220441
rs543537718	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61882052	CAAACATCCGAAATC[C/T]GAAATGCTCCAAAAT	220441
rs543566490	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851979	TATCTATAATATCCT[C/T]CCTATGACATATATG	220441
rs543624052	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61818622	TCAGGATCAACTACA[C/T]AGCTATCCACTAATT	220441
rs543633455	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61877726	TGCAATAAGGCTGAT[A/G]CTGCACAAGAAAAAA	220441
rs543730174	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869645	GGTGCCAGGAAGACA[A/C]CACAGATCATTAGAA	220441
rs543736392	in-del	-/A	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61827497	TTACTTTCACACATT[-/A]AAAAATATATATTTC	220441
rs543768854	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877179	CATCCACATGGGCAC[A/C]AAATGAAACCATTTG	220441
rs543787933	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61873070	TTGGGGTTCTGTCCC[A/G]GTTCTGCCACTTGCT	220441
rs543794733	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837881	TTTCCTTCAGACTTT[A/G]CAGGGATAGCCCACA	220441
rs543832425	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878552	AGACAAGATTTCTGT[C/T]TTAGTCTGTTTGTGC	220441
rs543833878	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61834791	ATGATATCTCCTCGC[A/T]GAATGGTAAGTTACT	220441
rs543842791	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825457	CACTCCAGAGATACT[A/G/T]GAGAGAGAAGAAAAC	220441
rs543879724	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61867842	CTATAAAATGGCCAC[G/T]AATGTCCAGTGCACA	220441
rs543901994	in-del	-/AGAG			intron-variant	RNF152	GRCh38.p7	18:61844027	AATGAGAGAAAAGAA[-/AGAG]AGAGAGAAAGAAAAA	220441
rs543913420	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844362	TCATGAGCAAATATC[C/T]TTTATAAAATCTCAC	220441
rs543932056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879353	GATTTAAAGTATACA[C/T]GAGGAAGTGCATAGG	220441
rs543938758	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875888	CTTCGTCCCTTCCTG[C/T]CCCAATCCATATTGA	220441
rs543965662	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825408	AAGGACATTTGGAAT[G/T]TAAGGAGCCTACAAG	220441
rs543992407	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864285	TCAGTGGGGTTTCTC[A/G]CAACCCCCTCTCCGG	220441
rs544029789	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857617	ATCTTCCATCTCATC[A/G/T]CCATGTTCTGACGAT	220441
rs544065764	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852545	CAAAACTCAAAAGAA[C/T]ATCTAGATTGTCAGT	220441
rs544071206	snp	C/G	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61861759	GGCATGTGCAGAGAT[C/G]ACATGGTGAGAGAGG	220441
rs544071927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873601	CAGCTGCCAAAGTGC[C/T]GGGATTACAGGCATG	220441
rs544105497	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61855355	TAGTGATGGCAGAAG[A/C]GGCCTGTTTGGAGCA	220441
rs544106167	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870146	ACGTTCCTGCACCCA[C/T]ATTTATCACGAATAC	220441
rs544121740	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830887	GTTAGAGATAGCCAA[C/T]ACTCTCTGAATCTTG	220441
rs544125623	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877011	GACTGACAGGTATGG[C/T]GAAACTCAGTTGGGG	220441
rs544231128	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853710	TTTGACTATTCTACC[C/G/T]CTTTTTCATAAAAAC	220441
rs544234388	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828582	GGTGTACACCATTGC[A/T]CTGGCAAATTTATGT	220441
rs544277934	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834319	CACACTGCTTTCAGC[C/G]CAAATGTCTATCACC	220441
rs544294978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827081	TCATAATGATAGCTC[C/T]GGATTAAAGGTAATT	220441
rs544303526	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846635	AGGGTGTAAGCTCCA[C/T]GAGTACTTGCTGCCA	220441
rs544316744	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61860119	AATGCCAAGGACTGC[C/T]GACAGCACGAGAAGC	220441
rs544452324	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855633	TGGAGCTGCCTGCCC[C/T]GCTGCAGCCCCTGGT	220441
rs544464408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867073	GGAGAACACCTAGAT[A/G]CTCGCCAGCTGAAGT	220441
rs544482310	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893170	GCAGAGCGCCTACTA[C/G]CAACAGTAAGCCCTA	220441
rs544504993	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61860908	TTAACAAAAAATGTT[C/T]AAAAGGTAAAAGAAA	220441
rs544513652	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829143	GTTAAGATTAACATG[A/C]ATTCATACATGTTGA	220441
rs544523545	snp	C/T	1.64977e-05	0.00287203	missense	RNF152	GRCh38.p7	18:61816168	AGGGGCAGCATGTAG[C/T]ACCCATTGCTGGGAA	220441
rs544531188	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844233	GGAAGGAGGGAGACG[A/G]GAGGGGAGGGGAGGG	220441
rs544546850	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822797	AAATTCAATGGTTGT[A/G]TTGAGAAAAAAACTC	220441
rs544588976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859462	GGGAGCTGCATTCCC[A/G]TGCAGAGCAGGAGAT	220441
rs544667650	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61884392	GGTATCAAGAATTGA[A/G]AGAATATCAGATACA	220441
rs544674715	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61832368	TAAAAGTAAAAATGT[A/C]TATTTTTACAATATA	220441
rs544677904	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810452	GAAGTTGGAGACCAG[C/G]CTGACCAACATGGAG	220441
rs544689647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871745	GGTAGGGACAACTCA[C/T]GGCCCACCTTGGAGC	220441
rs544709808	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812377	TCACAGGTTATACCA[C/T]CACATGGTTTAACCT	220441
rs544723792	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61820515	GACTATGATTGACTC[C/T]ACTGAGATGTAGCTG	220441
rs544729253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885290	CTCAGCCCTATTCAC[C/T]ACCTTTCAAACTGAG	220441
rs544743762	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61892385	CAATTAGAGCACTGG[A/G]CAAAAGTACAATCAG	220441
rs544793479	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847306	ATGTGCTATTTCTAT[G/T]TGCATGGGGTCTGCT	220441
rs544796763	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61885588	GCTGGAATTACAGGC[A/G]TGAGCCACCACGCCC	220441
rs544805347	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61829911	TAACCATTATAATGG[C/T]GTTATTATTGCTATT	220441
rs544812655	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815668	CAGAACAATTCACCT[C/G]GTATCTTGTTGAGAC	220441
rs544841120	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828558	GCCTCCAGAGTAGCT[A/G]GGACTACAGGTGTAC	220441
rs544853014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866911	CAACACAAAAAAAAC[A/G]GACTTAGGGGCTTGT	220441
rs544954072	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808810	CATGGTTAAGAGGAT[C/T]CTAGAGTCTGTCTGC	220441
rs544963020	in-del	-/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892785	CGCTACCCAGATCGT[-/G]GGGGGTTACCTGTAT	220441
rs544974458	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833840	ACCTAAGGTGACCTC[A/T]CTCAATTATAGCTAC	220441
rs545064217	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61834224	TATCTCATCTCTTGG[C/G]ATGCTGTCCTTTTGG	220441
rs545076288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833111	GACTTCTACCAACAG[A/G]AAATTACTATTTCCT	220441
rs545118120	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872512	TTAACTCCTTGCAGT[C/T]CAATTTTTAATCACC	220441
rs545143097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840299	GTCTATGGTATTTTG[C/T]TATAGCAGCCTGAAT	220441
rs545149690	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825824	ATGTACAAATTTACA[G/T]TTTAATAAAATGAAC	220441
rs545182785	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847566	TCACTACCAAAACCA[C/T]GGTGTAAACATTTAT	220441
rs545256982	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61857188	GCTCTGTCTCCATTA[-/T]CCCCAACACTGTAAC	220441
rs545299392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866462	CACACTCTCGCCCGC[A/G]TTTCTGTGCTTTGAG	220441
rs545375439	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61820478	GTCTCCAGGTGAAAG[A/T]GCACAGACAGCAATC	220441
rs545379545	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852721	TGTCTTGGGGGTGCT[G/T]CCTGGACATCAGGAC	220441
rs545393067	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61862543	AGTGTCATGAAGCTT[C/T]GGTAAAAAAACCCAA	220441
rs545429621	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863128	GTGTTGCCCGTAAAA[A/C]ATTTGCTCTTGAAAA	220441
rs545429657	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856275	GCTGGAGAACAAACA[C/T]AAGCTGGAAAATGAC	220441
rs545430583	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61820035	CAAAAAAAAAAAAAA[A/C]AAAAAAGAATCCGGC	220441
rs545451760	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823522	CAGGCTGGTCTCGAA[A/C]TCCTGACTTCAACTG	220441
rs545472785	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829942	AATATTCTTACTATT[G/T]TAGCCATTTGAAAGT	220441
rs545477939	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858581	TCTACTGCAGCCCCT[C/T]CACTTCCCCCAGTGG	220441
rs545553425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874361	CGATTACAGATACAG[A/G]ATTCAGCTACCAAAG	220441
rs545573093	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853613	TACCTTTTTTAGCTG[C/T]CAGTGGCTGCCTGCA	220441
rs545640084	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807895	GTTCTTTGGCCTCTC[A/G]GAGGAGCTACTTGAA	220441
rs545700834	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815200	CAGTTCCATAAACAC[A/G]TAGCAAGCTCTAATT	220441
rs545713641	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814248	ATTAAATTGTCTTGA[C/T]CTCACAGGGCTATTT	220441
rs545725032	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843733	GTGATTCCACTTACA[A/T]GAGGTACTTACAGTA	220441
rs545742110	in-del	-/A	0.0115144	0.0749975	intron-variant	RNF152	GRCh38.p7	18:61840950	TTGACTGCTCTTCCC[-/A]GCTTCCATCTCCAGA	220441
rs545754347	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814808	AGACTCCAAAACCAG[A/G]AGAAAAGACACTCTT	220441
rs545809757	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61885811	ATTGAAGCCTTTAAT[G/T]ATAAACGCAGGTGGG	220441
rs545816401	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860480	ACAGCCATCAGAGCA[C/T]TGTTGCACTGCAACG	220441
rs545865693	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823031	TCCAATTAGTGGCAA[C/G]AATGGGAATGCCCGG	220441
rs545870759	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61883539	TAGATCTCTACAAAG[C/G]CTGCTTCAGGATGTC	220441
rs545878209	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF152, LOC105372159	GRCh38.p7	18:61894420	GCCGCCAGGCGCTCG[A/G]CACCGAGCGAGAGCT	220441
rs545906945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848850	CTCCTGCCAGTGGCC[C/T]AACCCAACATGAAGC	220441
rs545907202	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831129	GAGATTAAACCTTAA[A/C/T]AGCACTCAAATTCTT	220441
rs545944111	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845618	TGTACTTTAAGACAT[C/T]GAAGGGTTTATGTGA	220441
rs546055728	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890488	GTCCTTGAGTGACTA[C/T]GATGAGCAGGGTCCA	220441
rs546073676	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61817833	GGGAATGTCCTCTAA[C/T]GCTCCACTGGCATTT	220441
rs546099910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849765	AGAGAAGTGGTCTCA[C/T]TATGTTGCCCAGGCT	220441
rs546113414	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811000	TGCACCGATAACTTT[C/T]GAACTTCTATCTTCC	220441
rs546151609	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811670	ATGCTTGCTCTTATA[C/T]TTGCACCTTACTAAT	220441
rs546169572	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848323	AGATATCAGTGCTTC[A/C]ACAATTTTTCTAACC	220441
rs546208256	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841819	TTTCAGTGGCAAGGC[A/T]GTAGAACATGGGTCA	220441
rs546208899	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855557	GCCCGCAGTAGAAGC[C/T]ACGTGCAGTGCATCT	220441
rs546221166	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886502	TTGATGCTTTAATAC[A/C]AAATAGGCTTTTTGT	220441
rs546241248	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866665	CTCCTCCATGTCTCC[A/T]CTCCCTGCTGTGTGC	220441
rs546284400	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61860777	AATAACAGCTCCATG[C/T]GTGTATTACCCTGAA	220441
rs546316361	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893364	CTGTCCGCCACCTCA[A/T]CAAGTCACCGCCACC	220441
rs546321549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854952	ATAACTCACAGACTG[C/T]CTCAAATGCTACAAA	220441
rs546328866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867140	AGGTGGGAACTCAAG[A/G]GTTACCCATGCATGG	220441
rs546359436	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61856305	CACGGGGAAATACAC[A/G]ATGGGTTCCTGTCCT	220441
rs546363347	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873788	TTTTCTGAGGAAATA[A/G]CACTTCTTTCCCCAC	220441
rs546398527	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61880650	TCATGAAATACATTG[C/T]GGAATCCAAGATAGT	220441
rs546418443	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839506	ATTACAGAAGCAATG[C/T]TATAATGTTCCCACT	220441
rs546466056	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893817	GGACCGGAGCTCCAG[A/G]GGGCATCCGAGGACT	220441
rs546540609	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855285	GAGTCAACCTTAAAA[G/T]TTTAATAAAATCAGG	220441
rs546546277	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880008	CACAGCTTTTTAGTA[A/G]TGTATTCCGAAAAAT	220441
rs546552766	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808133	TCATAAAATCAACAT[C/T]ACCACATATACAAAG	220441
rs546577087	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809760	TAAAAAACCTTAGAT[C/T]AGAATAATAAAATCG	220441
rs546578397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846996	GACAATCACACCTCC[A/G]TCAAAATATTGTTAT	220441
rs546661166	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882336	TTTGCCTATAAAATT[C/T]CCCTTCCAAAAACAA	220441
rs546688898	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846171	TTATATTATAGCACC[A/T]GAAAGGACAAAGATA	220441
rs546705429	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61821736	TGACAGACAATTACC[A/G]CCTGAGCTCCACCTC	220441
rs546746827	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859644	AGCAGTTTGGGAGGC[A/C]GAGGCGGGCAGATCA	220441
rs546767245	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814956	CACCGCTTCAGAGAC[G/T]TGACTCATTCATGCC	220441
rs546783772	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853766	AGATATTTCAGGATA[C/T]ACTCACCATTTCAAC	220441
rs546800565	in-del	-/GTGT	0.0135825	0.081282	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810273	TACAGCTAAATCGTG[-/GTGT]GTGTGTGTGTGTGTG	220441
rs546809499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841984	GTTCCAATAAAACTT[C/T]ATTTACAAAAACATG	220441
rs546828903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834382	TGGCTTAGACACCAC[C/T]TCTATGTTCTCCTAG	220441
rs546842119	snp	G/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61842528	ACCTGCAAGAGACTC[G/T]TCTCTGGCCTCTCTC	220441
rs546892200	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872656	CATTCTACTGTAGTG[A/G]ACTTCCCTCAAAATA	220441
rs546915047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872026	TCACGGTTCTGCAGG[C/T]TGTACAGTAAGCATG	220441
rs546982546	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61844097	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	220441
rs546993249	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884206	TTACACTAACTCAAT[A/G]AGGTCGGTTCTCCCC	220441
rs546997213	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884722	CCACCACCATGCCTG[C/T]CTAATTTGTATCTTT	220441
rs547026819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878941	AACTTACACTAGAGC[C/T]GGAGAGGCAACCATA	220441
rs547060336	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	RNF152	GRCh38.p7	18:61807574	TTGAAATTCATTGAT[A/G]TGATCCAGTTATCAA	220441
rs547087712	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811955	GCCTAAAATCTATAA[A/G]CAACAGTTCCAAAGG	220441
rs547113807	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61891238	AACACATCTGAGGGT[A/G]GGGAGCCTCCTTCTT	220441
rs547155596	in-del	-/T	0.275464	0.2487	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895503	TTTTTACTTTTTCTG[-/T]TTTTTTTTTTTTTGA	220441
rs547231190	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859379	GCATCAGTTTCACAC[A/G]CTGTTCCCAGGGCTC	220441
rs547233950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824491	AGAATGCGCATTTAT[A/G]TGAGATGGGGGAGTG	220441
rs547234190	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61881102	TATTTTTAGTAGAGA[G/T]AGGGTTTCCTCATAT	220441
rs547251022	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61835142	CTACATATGATTTAA[C/T]TTTTGACCCAGCAAA	220441
rs547259827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878154	CACATGGCCCCACCT[A/G]GGTACAGAAAGTAGT	220441
rs547287959	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61833927	AAATATCAGATGCGC[C/T]AAGAATACCAACTCC	220441
rs547383196	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818266	TATCTCTACAAAAAA[C/T]ACAAAAACTAGCCAG	220441
rs547416833	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881783	GTTTAGCATCTCCAC[A/G]CACAAGTTCTACAAA	220441
rs547425316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869465	AAATGTGGAATGCCC[C/T]GTCACCTCACCACAG	220441
rs547427635	snp	G/T	0.386504	0.209444	intron-variant	RNF152	GRCh38.p7	18:61829510	GGAGAGAGAGATATA[G/T]ATATATCAGGGGAGG	220441
rs547469843	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61839819	AGAATGGCATGAACC[C/T]GGGAGGCAGAGCTTG	220441
rs547532079	snp	A/G			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868176	CCCACTGTAGAGGTT[A/G]GCCTTCGGGTGTTGC	220441
rs547555373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888878	GAAACCACTTTCATG[C/T]CACAAGAGTCCTCTA	220441
rs547556989	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869825	GCCACTTACCCACCA[A/C]CTTCCTCAGCTTTTA	220441
rs547557802	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61817494	GTTCTGCATCTGCGA[C/T]CAAATGACATCAAAA	220441
rs547560418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880365	AAATGCTTTTGAACC[C/T]TAATCCCAGTTGTGA	220441
rs547588562	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61865285	TCAGCTTGAAAATAT[C/T]AAACCCTACTGAAAA	220441
rs547597178	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61888971	AGAAATGCATTTTGG[C/G]GCTTCCCAAATATAG	220441
rs547652904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856397	TCTGCCACAGCGCCT[A/G]CTTCTTTCATGGCAG	220441
rs547670699	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61816766	CGCCCAGTGAAAGGC[A/G]AATGAAAGTTGTCTC	220441
rs547686682	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896175	AAGTAGAAGACTTCA[A/G]GAGTCTTTATTTTAA	220441
rs547783313	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874483	ATAATGTGCAACTAT[A/T]TTAAAAAGCATTAGA	220441
rs547826176	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868129	CTCCAGTCATTTTCC[C/T]CGTAGCCAGCACAGG	220441
rs547827975	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837836	AAAGTGTCTAGCAGA[A/G]TTCCTGGCTCACAGC	220441
rs547849083	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61835959	TTTAGAATGGGAGAA[G/T]GTGAGAAGGAACATA	220441
rs547883526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849291	TGACATGGCCAGAAA[C/T]TTTCCTTTTTAGAAA	220441
rs547925897	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835933	CTCACTGTGGAAGGA[A/G]AGACAAAAATTTTAG	220441
rs547941589	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884952	ATTTTACACACCACC[A/G]TAGGTGAATGGATGG	220441
rs547964892	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810518	CTGGGCATGGAGGCG[C/T]ATGCCTATAATCCCA	220441
rs547999175	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875200	GGTAACACCTGGAGG[C/T]TAATGAGTTAACCAA	220441
rs548055505	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823644	AACAGGGAATAGGGC[A/C/T]GGCGATGCTGACAGT	220441
rs548062744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862215	TCCTCTCTGCCTCCT[A/G]TGCTTACAGAAAGGC	220441
rs548107657	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61874629	ATGGTGAGGTATATC[A/G]GAGTTTATCAATTAT	220441
rs548165166	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896129	AAGAGTAAAAGCTGT[A/G]TCCATGTTTTAGAAG	220441
rs548176354	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864679	AGTTGGTTCCTCTGG[A/C/T]GACCAGCTGGCACTC	220441
rs548213072	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837480	GGGTAAAACGTCATG[A/G]TGTCTGCCAATAAGA	220441
rs548225361	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828908	GATTGATACTTCACG[C/T]GGGAGTATCAGGTTG	220441
rs548235142	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61862586	CAAGGAGCTTCCAGA[C/G]AGCTGAACATGCTGA	220441
rs548271226	snp	G/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61856342	ACTACAAGGCTGGGG[G/T]TCCCAAGAGTTAATT	220441
rs548304223	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894946	GGGTGGGGCCCCGCT[C/T]TCCAAAGAGGCCCGA	220441
rs548327113	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837246	AGATTGTTCTAGATT[C/T]TAAGAGACTACGGAG	220441
rs548339829	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823105	CAATCCTTCCAGGAC[A/C]CAACTGCTGCATACA	220441
rs548355168	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888633	ATGTCAGTAGGTGTA[C/T]TAAATGCATTTTCCA	220441
rs548377930	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886561	ATTGCAGGTCACAAC[C/T]GCTACATCAGCCAGC	220441
rs548388009	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61887149	GTTGGAAAGGAAGTT[A/T]GGGGTCAACCTGGGG	220441
rs548414151	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830857	AAAGGTCAGTGAAGA[A/G]AGTGGCATCTGAAGG	220441
rs548450897	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61816915	TTAAGCAAGCTCTGG[G/T]TCATCCTTCTAAAAT	220441
rs548473796	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862032	AAAATGAATACAACT[C/T]CCTGAGGCCCTCAGA	220441
rs548603969	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61819679	TCAGGCCATATTCCA[-/C]TGGAGGTGCTGGGGA	220441
rs548606621	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825961	TTTTATCTATGTCAG[G/T]GACCCACAACCTTTT	220441
rs548611169	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835779	TGTAAAGCAGTCTTG[A/G]ACTTTACCTATTTGG	220441
rs548619896	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873386	TCTGTTGCCCAAGCT[A/G]GGGTGCAATGGCGCT	220441
rs548688141	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61834531	TTGACCTTTATTTAC[C/G]TTCATCTGCCTCGGC	220441
rs548711785	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877201	AACCATTTGACTTAC[A/G]TATTTTGGTCAGGGG	220441
rs548730728	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820222	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	220441
rs548853571	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61819499	AATAGTGATGATTAG[A/G]ACAGAATGATGAGAT	220441
rs548853643	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826555	CACATGTTGTATGCA[A/T]ATATAAACTTTTTTT	220441
rs548856171	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873855	GAACAGTCCAAGTCC[A/G]GGGTAGCAGATCTTA	220441
rs548900643	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61826099	CTCAAGGAATGAGCA[A/C]GGCTATGTTCTGTGG	220441
rs548941798	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868013	TTCTTAGAACTTAAC[C/G]AGCCTCCTAGGGGCA	220441
rs548948964	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61891845	TACCAAGGTGTTACT[A/G]CAATGTAAAAGAGAG	220441
rs548967917	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871086	TTTACCTTAGGCTTC[A/G]ATTCACACCATTGGC	220441
rs548985569	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869076	AGAATATTCTAACAT[C/T]TCAGAGGTAATCTCG	220441
rs549019825	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61869407	GGCCATGGAGGTATT[A/G]TCTCCTGCACCTGAC	220441
rs549048901	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882840	TTGGAAAGTAAACAC[C/T]GGGTGCTGAGTACAC	220441
rs549108848	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876849	GTCTTATGCTCATTA[A/T]TATGCAAATGCTTTA	220441
rs549128242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889718	TACCCTAAACACATT[C/T]CTGCCCCCTTCAGAT	220441
rs549198362	snp	A/C	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61886705	TGATGACAAGACATC[A/C]TGGGACATCTCTTCA	220441
rs549250567	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61864700	GCTGGCACTCTGAGG[C/T]CAGCTAAGAGCCCAC	220441
rs549253487	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863303	AGCCAGGCGTGGTGA[C/T]ACACGCCTGTAGTCC	220441
rs549333364	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876994	CTGGAGACAGGGATT[C/T]TGACTGACAGGTATG	220441
rs549337173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61838433	ACTTACATCCTCCCA[C/T]TTTGGATCTGCACTT	220441
rs549340177	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61865222	TTGGATACCTACCAA[C/T]AATCATTCTGGGGAA	220441
rs549360729	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818109	ATATAATGTGTTAAC[A/C]ATCAAAATTAAGAAT	220441
rs549362548	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824963	CAGACAGGCAGGCAG[A/G]TAGAGCAAATAAAGA	220441
rs549400270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818709	GATATAAATCAGACC[C/T]AGATTCTACCCGAAA	220441
rs549400573	snp	C/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892779	CCCAGGCGCTACCCA[C/G]ATCGTGGGGGGTTAC	220441
rs549412047	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61831971	TTGATCTGTAATCAT[A/G]CTCACACATATACCA	220441
rs549470248	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61825792	ATCTACAGGACCCCC[A/G]AAGGCCCAAAGTTCC	220441
rs549534711	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825926	AATTTGTTGGCTTTT[A/T]AAAATATTTTCCCAT	220441
rs549619616	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857679	TTCCATATCCTCCAG[A/G]GACTCACCAGTCATT	220441
rs549627276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845273	TTTTCTTATTCACTT[A/G]TGGAGGTGACAGTTT	220441
rs549635296	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809559	ACAGAAGACTTTCAC[A/G]TGGGCTACTAGCCCT	220441
rs549643024	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825164	CACCTTGTGTACTAT[A/T]CAAGGAACCGGCGTT	220441
rs549646988	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883882	GAAGGCCTATCATTT[C/T]AAACTCAGAGCCACT	220441
rs549675998	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61818898	GCCTAGAGATGGGAG[A/C]GCTAAGTACTTAGAC	220441
rs549709527	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61838397	AGAGATCAGCCCTGT[A/G]ACCAGAGACGGAGGA	220441
rs549838415	in-del	-/CCCAAGCGCCTGAGCTGC	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61851414	AGGAGAAAACACTTA[-/CCCAAGCGCCTGAGCTGC]CCCAGCTTCAGGGGT	220441
rs549874821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823839	CAACTGTGGGCCCAA[C/T]TGGCCTGGCTGCAGC	220441
rs549911803	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817537	CAGGATGCAAAGCCC[A/C]TGTATACCGAGGGCC	220441
rs549945099	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882293	ACTGTGTGTGTAAAA[A/G]TAAAGGCAATTTATT	220441
rs549952828	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819456	GAGGCTATTACATTA[G/T]GCAAGAGTTAAATGA	220441
rs549974883	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61842289	AAACATTTCCTGAAA[A/G]CCCCTTTGTGGCCTA	220441
rs549989948	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61868316	GCAGCTACACTGCTC[A/G]GTATCAGTTCAGAGA	220441
rs550052869	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61868801	ATAAATCAGTAGTGT[A/G]CCTTGTAGTTATGTG	220441
rs550053148	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61891074	ACCCAACCCCAACCC[C/G]TTGAGTCCATTATCT	220441
rs550053520	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811338	TCAAACTGAATTTTC[C/T]GCTTCCTTTTATTTA	220441
rs550067506	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61876779	TGTGAGGAGTAGGCA[C/T]GCACTGTAAGCAAAA	220441
rs550131903	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61869288	GCTGTCAGGGGTCTT[C/T]TTCCAATCATACTTC	220441
rs550149852	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876739	AGACATTAATAGAAC[C/T]GTCTACTCTACCCCG	220441
rs550211285	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61874390	AGTGTAGTTAGCATG[-/CA]CAGAGTGGAAAGAAC	220441
rs550217406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871980	AACACTTAAGACTGG[A/G]TAATTTATAAAGAAA	220441
rs550309936	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821533	ATGTGCATCAACTAT[A/G]GAAGAAAGAATGGAA	220441
rs550350354	snp	A/T			missense	RNF152	GRCh38.p7	18:61815978	CGACCAGGTGGAGCT[A/T]TTCACCACGCCCCGC	220441
rs550366513	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61836728	TAAGACACTGAATTT[A/T]AAAAAAAAATCCTTG	220441
rs550397502	snp	A/G	0.00478085	0.0486577	intron-variant	RNF152	GRCh38.p7	18:61850910	ACCCCTGAATGGCTA[A/G]TGCAGCTCTGGGCAC	220441
rs550434286	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851400	GGAGGACGGAAAAGA[C/G]GAGAAAACACTTACC	220441
rs550452476	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854721	TCTCTCTCTCCTTTC[A/G]CTAGCACATCAGGGA	220441
rs550502725	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61857161	TGACTTGCATTATAC[A/G]TCAGGGTTCAAGCTC	220441
rs550533981	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859951	GCCTTATTTGGAAAA[C/T]GGGTCACTGCAGATG	220441
rs550555168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852855	GGTACTAATGGCCAC[A/G]AATAATTTCACAATG	220441
rs550566283	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828289	GCTATGTTGCCCAAG[C/T]TAGTATGGTGACTAT	220441
rs550592312	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815743	AACCCAGAGGCCAGC[C/G]CTCAGCACCAAATGG	220441
rs550659713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890428	CTTCCCGATGCTGCA[A/G]TGATCTTGCAAGCTC	220441
rs550696313	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61866044	TCCCACTGCCTGGGT[C/T]CATTCTTATGTCTGC	220441
rs550698203	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845526	GAAGTTTGAAATTTA[C/T]AGTCAAAACAGTTGC	220441
rs550706892	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61893012	CTGGAGCGGGTGCAC[C/T]AGGGAGGTGGAGCAA	220441
rs550791075	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855050	TAAGCTAATGGTGGT[A/G]GGGAGAGGGAACTGC	220441
rs550793170	snp	A/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61847820	CTTCACACCTACTCT[A/T]CCCTCTGCTTGGAAT	220441
rs550802203	snp	A/G/T			intron-variant	RNF152	GRCh38.p7	18:61843646	AGGAAATTCTGACAC[A/G/T]TTACGACATGGGTGA	220441
rs550866065	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853891	ACTTCTCTGGGGTCC[A/C]TTATTCACCACAGAG	220441
rs550902782	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854593	ATTTGGAGCCTCAAT[C/T]AGTCATCTTTTGAAC	220441
rs550906497	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877566	GAAAACTGCCAGTAC[A/T]CTTGAGGTTTTATTA	220441
rs550974836	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891073	CACCCAACCCCAACC[A/C]CTTGAGTCCATTATC	220441
rs550989311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846047	TGCCCTTTATGAACC[A/G]GAAAATGGGCTCTCA	220441
rs551007334	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879879	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	220441
rs551018671	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895463	CCCCCAAGTAGCTTA[C/T]TGAAATGCTTCTGCC	220441
rs551034868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884681	CTTCCTGCCTCAGCC[C/T]CCAGAGTAGCTAGGA	220441
rs551156325	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61833472	TTCTACCAAGAACTC[C/T]TGTCCTTCAAATGAT	220441
rs551168020	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808188	AAAATACCATATATT[A/C]AAATTGGGTTCATTG	220441
rs551185325	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61856144	ACTCTAAAAGCTTCT[A/T]AAAGCTCCATTAACA	220441
rs551222069	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859039	CCCTTTCTAACCCAC[A/G]TGGGCCCATCTGATG	220441
rs551244078	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814614	TAGTTTACCTTGCCA[C/T]CTTTCTTGGTAAAAA	220441
rs551311404	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826642	GAAGAACTTTCCCTC[C/T]GCAACAGTTCTAATA	220441
rs551369883	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820769	ATACTATTTACCTTA[A/C]CTTCTACATCACAAT	220441
rs551436185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863959	ATGTATTTTAATCTT[C/T]CTCTTTCTGAAAAAC	220441
rs551482305	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851625	AAGTTTCAGAGCCAA[C/G]GTTTAAACTGAGACA	220441
rs551498430	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864496	CTCCCCCAGCTCCTC[A/G]AAGTGTTCACCGACC	220441
rs551550591	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61853859	CCAAGGATGAGGTTC[C/T]AAGGATGAGGACAAG	220441
rs551597451	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61826149	GAGTTGGTATAAAGA[C/T]TATTTTAAGCTGGAG	220441
rs551675236	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865902	AGCTGAGTGTCAATT[A/T]CATATCTCCCTGTTA	220441
rs551675948	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864890	CCAGGCGTGGTGGCG[C/T]GTGCCTGTAATCCCA	220441
rs551684867	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876915	AAGTTAAGACACCTA[A/G]CAGGATATTTACTGG	220441
rs551696141	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61883053	AGCACAGGAAACCCA[A/G]AGCATATCTAGATGC	220441
rs551710125	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859749	CCAGGCGTGGTGGCA[A/G]GCGCCTGTAATCCCA	220441
rs551765732	snp	C/T	0.00676609	0.0577691	intron-variant	RNF152	GRCh38.p7	18:61889833	GCGGTTCCAAACAAA[C/T]TCAGGAAGCCTTAAA	220441
rs551810502	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813477	ATCTACCATACAGCC[A/G]ATTAATTTTGCACTG	220441
rs551829441	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861350	CAAATACTTATTGTG[A/T]GTGTTACAATTGCTT	220441
rs551868153	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861902	TCCTGTGACCTAAAC[A/G]TCTCCTATTAGGCCC	220441
rs551888657	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818854	TCCCTTGTAACTAAG[A/G]TCTTGTCATTGCCCA	220441
rs551917974	snp	A/C	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61849172	AACAGGGGAGTACTG[A/C]CCTGCGGGGGCTTCA	220441
rs551957665	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881059	GCTGGGATTACAGGC[A/G]CATGCCACCACGCCC	220441
rs551973986	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61874060	AATAAGTGTACTTTG[A/T]CTAATTAATTTAATT	220441
rs552016378	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852189	TATGATTATTTCTCC[A/T]CCAAACTGGAAACAT	220441
rs552033698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832877	CCAGTTGGCATATCA[C/T]GACCTTCACTCCACA	220441
rs552058172	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877506	TTGCCACAAATATCT[C/T]AACTCGAACTTGTGT	220441
rs552091117	in-del	-/TT/TTT	0.273318	0.24891	intron-variant	RNF152	GRCh38.p7	18:61830025	TTTCCAGAGAGCTTC[-/TT/TTT]TTTTTTTTTTTTTTG	220441
rs552106605	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894003	CGGTCCAGAAGATCT[C/G]CCCAGTTACAGCAGG	220441
rs552120980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816670	AACATATCTAATGGA[C/T]TTATACCATTGCTCA	220441
rs552169159	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61887542	GCCAACATGATGAAA[A/C]CCTGTCTCTACTAAA	220441
rs552207877	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842632	ATTAGTCTATTTTTG[A/C]GCTGCTGATAAAGAC	220441
rs552209799	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812619	TTCTCTTCCTTATTT[C/T]AAGATCATTAATAAA	220441
rs552217315	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61855712	ATCTCATCACTCCAC[A/G]TCTGGCTCGCCCTTG	220441
rs552254010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831554	GGAACTGAAATGTGA[A/G]GTTATGGATTATTCA	220441
rs552284456	snp	A/G	4.95111e-05	0.00497525	missense	RNF152	GRCh38.p7	18:61816264	TCGTCCGGGAGCTGC[A/G]ACACGGAGAAGCCGG	220441
rs552307798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843219	TTCAACTCGTGCACA[C/T]CCTACAGAAAAGCCA	220441
rs552308688	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828804	TCTAGGTTTGGGGAA[A/T]CTGAAGAGAAAAAGA	220441
rs552412245	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847737	CAAAATGGAATTCCC[A/G]GTCTCCCTCCCACCC	220441
rs552445529	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836553	CGGCTCTCTGCAAAC[C/T]AGAAAGAAGGTTCCC	220441
rs552482225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867185	TTGGGGACCGGGTGC[A/G]GTGGCTCACACCTGT	220441
rs552485546	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888143	TCTCCACTCCTAGGC[A/G]ATCACAAGCAGCCCC	220441
rs552513353	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841599	GGGGTTACAAGTCAT[C/T]CTGAGAAAGTGATAA	220441
rs552539977	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822484	TTGAAAAGGTACAGG[C/T]GTGACAAAGTGCGCG	220441
rs552562539	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61885228	CCCCAGAACAACACA[A/T]CTGCAAAAGAATATC	220441
rs552564747	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61893037	GAGCAAGGCAGATGA[A/G]GTGTGGAGGGCTGGC	220441
rs552614768	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61851167	CTTACCTTTCTGACC[C/T]ATCAGAAACAGACAG	220441
rs552643158	snp	G/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61873286	CAAGTACAAATATCA[G/T]AGATATTTAATATTT	220441
rs552682690	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884818	CCTGCCTCAGCCTCC[C/G]AAAGTGCTGGGATTA	220441
rs552796034	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61872721	TGATATAATGACTAT[C/T]ATCATGATTTTCGCA	220441
rs552831596	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853976	TTTTCAACTGAGAAA[A/G]CTCAGGCTCAAGGTT	220441
rs552868930	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61879560	GGAGAAAGCGTGTTC[C/T]GGGGAAAGGGAACTA	220441
rs552898717	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877811	CAGGAATACTGGCAC[A/G]GCTGCTTCAGCAAAG	220441
rs552949637	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870856	GATGCCCACCTGACT[A/C]CTAACCCATCACACA	220441
rs552983381	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61847191	GCAAGAAGTGGAGAG[A/G]ACAACACAAAAAAAG	220441
rs552985566	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61853591	CCATCGCACCTCACC[A/G]GTTCCTTACCTTTTT	220441
rs552998496	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825093	ACTAAGTCTTACCAG[C/T]TGCTGAACAGCTACA	220441
rs553017181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845686	CCCTATAATGCACTT[A/G]CAATCTTCATTCTTC	220441
rs553031487	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61838498	ATGAATCTCAAAGAA[C/T]CAAGATTCAATGAAA	220441
rs553031598	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879239	AACGATACAGTATAA[A/C]AACAACTTACATTTA	220441
rs553089390	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815187	CCTGTTGAGCTTTCA[G/T]TTCCATAAACACGTA	220441
rs553119565	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833517	AAACTCCTCTGCGTT[G/T]CCCTCTAATGGAATA	220441
rs553235372	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834198	TCTCATCTCTAAGCC[G/T]TTCTTTCTCTTATCT	220441
rs553239662	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871585	CATGCTGTTTTCACC[A/G]TATCATTAAGAAATG	220441
rs553273267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840886	AGCCTTTTCCCCTTC[C/T]CTACCCATGAAACCA	220441
rs553302403	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61873997	TTCCTAATCTATCTT[A/T]ATAAGCATAGTTTCA	220441
rs553312863	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854190	TTTCCTTTCACTCAG[C/T]TATCTCTGCTTCTCA	220441
rs553323063	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833080	CATTCCTCAGCTGTA[G/T]CTACTAAAATTCACT	220441
rs553345971	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836806	AAAGAAAGGCAGGAA[G/T]AGAAGGGGGATTACA	220441
rs553406072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826946	AAAGAGCTGAGCAAA[A/G]AACATAAACAATGGC	220441
rs553520570	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823496	TAGAGATAGGGTTTC[A/G]CCATATTGGCCAGGC	220441
rs553599748	snp	G/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811265	CTTAAAATCAAAATC[G/T]AGACTGGAATAAATA	220441
rs553650262	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821009	TGAAAGGTTCAGAGA[A/G]GACAGTGCTTGTTCT	220441
rs553650281	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814734	AAAAAGAATCACAGG[C/T]CATTTATTAAAATGC	220441
rs553670945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856878	AGCTATAAAGCTCAT[C/T]TTCAAAAAGCCATAA	220441
rs553708457	snp	C/T	1.65097e-05	0.00287308	synonymous-codon	RNF152	GRCh38.p7	18:61816092	GGACTTCTGCTGGCT[C/T]CCGGGCAGCAGGCGG	220441
rs553747851	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885607	GCCACCACGCCCAGC[C/T]GAGAGCGTTATTTTA	220441
rs553753720	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874762	TAGGGCTAAGCATAG[A/T]GGGGTATCTAATCCC	220441
rs553760116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830453	ATTTGCCTGTTCCAG[A/G]TACCTCATAAGAGTG	220441
rs553814253	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61875570	ATCTGGGCGTGGATT[A/G]CCCACGAAGGTCAGC	220441
rs553869926	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61821970	GTGCCAAAAATGTTG[A/G]GGACTGCTGCTTCAG	220441
rs553898836	in-del	-/A/AA/AAA	0.27893	0.24832	intron-variant	RNF152	GRCh38.p7	18:61817742	AGCATTCCTCATTGT[-/A/AA/AAA]AAAAAAAAAAAAAAA	220441
rs553926646	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890266	AAGTCACTAGTGCTA[C/T]TCACCCATATCCACT	220441
rs553968823	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817819	CTTCACTGAAGTTTG[A/G]GAATGTCCTCTAACG	220441
rs553988002	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860430	TGGTCCCATAAGATT[A/G]TAATGGAGCTGGAAA	220441
rs554055697	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61823923	GGGGACTCTGCTAGG[A/G]CATGTGCCAATTCTG	220441
rs554056640	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61818176	ACCTGCAATCCCAGC[A/C]CTTTGGGAGGCCGAG	220441
rs554122468	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855485	CCCTTTGGGGCTCTG[A/C]AATTCCTCGCATCTC	220441
rs554208712	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848676	AAAGCCCCTACTGAC[A/C]TCAGGGTGGAGGGGG	220441
rs554235443	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859494	CTGCCCTTGAAGAAG[A/G]GCCTGGAAGCTGCAG	220441
rs554256910	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61835527	GGAACAGAGAGGAAA[C/G]GCATGGGAGACCTCC	220441
rs554257914	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828996	AAAAGTACCATTTCA[A/G]TGTCAAGGGTGAGGA	220441
rs554269038	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866845	AGCCCATAGCTTTGG[C/G]ACCAAGGAATGCATT	220441
rs554293047	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895104	CTTAAAACCTAACTT[A/C]GACCTAGGGAGGTGC	220441
rs554354826	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860672	CAGTATTTTAGAGTG[C/T]ACTCCTACTTATTTC	220441
rs554356601	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867650	CAACCCAGGGTGAAC[C/T]GTATGTAAACCAGGC	220441
rs554362446	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61867015	ACTGCACATCAGGAA[-/T]TTTTTTTTCTCACCA	220441
rs554365479	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61886981	CTGAACTGAGGCTTC[A/G]ATGATAGGATAGAGG	220441
rs554369114	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866374	CTTATTACACACCAG[A/G]AGCTGGCAGCAAAGA	220441
rs554371425	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61842129	TCACATGTATTTTTA[C/T]CACAAGTTGATCATA	220441
rs554421970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887715	TCAAAAAAAAAAAAA[A/G]AAAAAAGAATGCTCC	220441
rs554470226	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868204	TGCTGTAGACTTACA[A/G]CATATATCTGTGTTA	220441
rs554493824	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	RNF152, LOC105372159	GRCh38.p7	18:61894310	GGCGGACGCTGACAG[A/C]GCGGCGGCGGCGCCT	220441
rs554504960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828459	AGACGGGATCTTGCC[A/G]TGTTGCCCAGGCTGA	220441
rs554516714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61816997	TAAATTTCTCTCCTT[A/G]GATCCTCTGACCTTT	220441
rs554538385	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61842732	GCCTCACAATCATGG[C/T]GGAAGGCAAGGAGGA	220441
rs554611878	snp	A/G	0.00438332	0.0466095	intron-variant	RNF152	GRCh38.p7	18:61841690	AAAACAGAATTGTGC[A/G]TATAATTTCATGGAG	220441
rs554630845	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61829236	GAGGCAGGAAGGAGA[C/T]GCAGGGCACAGCCTG	220441
rs554681927	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61866797	TCCCCTACTTGCCCG[C/T]TGTCCCCACCGCTGA	220441
rs554682337	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61819075	GGTAAGCGATTACAG[A/C]ATTATTTTCTATTCT	220441
rs554767979	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823444	GGGATTACAGGTGTG[C/T]ACCACCACACCCAGC	220441
rs554829172	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809358	AACAGAGGTATCAAC[C/T]AGATCCCCTTTAAGA	220441
rs554885359	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61854858	CTGACGTGAAAATAG[C/T]AGGCGGAAAAAAATC	220441
rs554902952	snp	A/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61818428	ACCCTGTCTCAAATT[A/T]AAAAAAAAACAAAAA	220441
rs554904849	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825251	AGAACCATATAAAGA[C/G]AACCATGAGAAAGAG	220441
rs554926644	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61822805	TGGTTGTGTTGAGAA[A/G]AAAACTCAAATGCAG	220441
rs554939374	snp	G/T	0.000399281	0.0141238	missense	RNF152	GRCh38.p7	18:61816054	AGAGGCTGCTGTTCA[G/T]CAGGGATGGTCACCA	220441
rs554947796	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814524	TCTTCATGAGCATCT[A/G]TAGATCATTACACAT	220441
rs554986807	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815448	ACACGGATTCGCAGG[C/T]TTAATTCTACTTGTC	220441
rs554994350	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61818956	AAGGGAGCCGAAGGA[A/G]TCAGGGGGAATTTAG	220441
rs555067338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824659	TGATCAGTAGCCTTC[C/T]CAGATGAAGAAAGAT	220441
rs555091582	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872327	GGGTGGGGACATAGA[A/T]CCAAACCACATCAGG	220441
rs555111341	snp	A/G	0.000181478	0.00952397	synonymous-codon	RNF152	GRCh38.p7	18:61816299	CAGCTTGGTGACACC[A/G]CGGCACCAGGGGCAC	220441
rs555117764	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876510	CATCATATACAGATG[C/T]TAGTCGAAGTCATGA	220441
rs555154459	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888152	CTAGGCGATCACAAG[C/T]AGCCCCCTCACAACT	220441
rs555173390	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893182	CTAGCAACAGTAAGC[C/G]CTAGGAAAGAAAGAA	220441
rs555181268	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886176	TTTAATCATTATTAA[C/T]GCAAGTAGGGGAAGC	220441
rs555219109	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889945	TCAGCCTTGAAAATA[C/T]CTAATGGCCTTTCAC	220441
rs555238869	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894104	CCCTCTGTCCGCCCC[C/G]GATCCGGAGCCGGCA	220441
rs555247741	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852383	GCCACCAGGACATAC[C/G]AATCTGTGGTGCTGA	220441
rs555413080	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858520	TACCTTCTCCCTAGA[C/T]TTCACATTCCAACCT	220441
rs555416759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864158	TCCATTTTGACCCTA[A/G]CTACCCGGAGTCACA	220441
rs555426662	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61838391	GACTCCAGAGATCAG[A/C]CCTGTAACCAGAGAC	220441
rs555431676	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895519	TTTTTTTTTTTTTGA[A/C]GATGGACTCTCGCTC	220441
rs555441491	snp	A/G	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61842633	TTAGTCTATTTTTGC[A/G]CTGCTGATAAAGACA	220441
rs555515061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888574	CCCATTGTAGGCTAA[C/T]GCGCATTTCTGGGCA	220441
rs555522887	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61843561	ATACCCAAATGCCCA[A/C]AGACAGATGAATGGC	220441
rs555528371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870055	ATATAACTTGTTATA[C/T]CATAAAAAAGTATTT	220441
rs555529433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856130	CTTTTCCAATTCTGA[C/T]TCTAAAAGCTTCTAA	220441
rs555546949	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863655	TCAAGCAATCCTGTG[C/T]AACCGTATGGCCTGT	220441
rs555553146	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889925	AAGCTCACAACCTCC[G/T]AGAATCAGCCTTGAA	220441
rs555599392	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818950	TACCCTAAGGGAGCC[A/G]AAGGAATCAGGGGGA	220441
rs555600001	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61820803	GGAAGTAGCTCAGCA[A/G]AGTGGGAAGACTGGA	220441
rs555614409	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890612	CTATCTTGCTGGTAC[A/G]TCACTGTTTAAAAAA	220441
rs555619222	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61839056	CCCACTCTGTGGCCA[-/A]AAAAAAAAAAAAAAA	220441
rs555637499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889050	TGCCTGGCCCTCAGC[C/T]CAACCCCAGGCACCC	220441
rs555702467	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892926	CTTCAGCCTGCAGTG[A/G]AATACATGCAGGAAG	220441
rs555734967	snp	C/T	0.0154538	0.0865337	intron-variant	RNF152	GRCh38.p7	18:61861565	AGGCATGACTGTACA[C/T]GTTACGCTTAGTGTC	220441
rs555781024	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824542	ATTTCTCCCTTGATG[A/C]CTTCAGCTTAATGAG	220441
rs555784673	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881355	AGAAATTTGTTTCTT[C/T]ACAAGTCAGAATCTC	220441
rs555786211	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862828	GTGGGTCAGAAGTTC[C/T]GAGGAGGCCCAGACT	220441
rs555839197	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61823941	TGTGCCAATTCTGTC[A/G]CTACAAAACTCAACT	220441
rs555902783	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863136	CGTAAAACATTTGCT[C/T]TTGAAAAGTAGTCCC	220441
rs555913105	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875114	CAGGGTATTGAAGGA[A/G]GAGTTAGAGTTTGAA	220441
rs555924023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857858	CATCTACATTCAAGA[A/G]CATTTTCCAAAATAA	220441
rs555925250	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817834	GGAATGTCCTCTAAC[A/G]CTCCACTGGCATTTC	220441
rs556015059	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869114	TATAAAATTTCCTAA[A/G]TTCACCATGTCTCTC	220441
rs556107263	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810197	TCTAATCCAATATTG[C/T]ATAACTCACAAATTG	220441
rs556142972	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869535	AGGAACACAAACTTT[A/T]GTGTTATTTCCATTT	220441
rs556150453	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890504	GATGAGCAGGGTCCA[C/T]CTGCCAACCACACTG	220441
rs556172014	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61887862	AAAGTTACACTTCCT[C/T]GGTAGGTGGGAATGC	220441
rs556315727	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61869767	CACGCACGCACACAC[A/T]TGCACACACCCGGAA	220441
rs556317375	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895223	GATAGTTCCATGCCC[C/T]TTGGTGCCTTTTTAA	220441
rs556350873	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871757	TCATGGCCCACCTTG[A/G]AGCTGCAGAGCCCTT	220441
rs556360498	snp	C/G/T	0.000211784	0.0102886	synonymous-codon	RNF152	GRCh38.p7	18:61816455	AGAGTCCTGGGACAG[C/G/T]GTCTCCATGGTGGAC	220441
rs556375530	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836865	TTTACCATCTCCAAT[A/G]TAATGACCAATTTAG	220441
rs556382199	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863389	GCAGTGAGCGGCGAT[C/G]GTGCCACCGCACTCC	220441
rs556402683	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818225	CTCAGGAGTTTGAGA[A/C]CAGCCTGGGCAACAT	220441
rs556540246	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807721	TCACAGGGGCTGCAT[C/G]AAGTTGTTCTGTATA	220441
rs556573866	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61887817	CACCAAGTGTGATTA[C/T]CTGGATGTCTAGATC	220441
rs556592163	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842876	ACGGGAAAGACCCGC[A/C]CTCATAATTCAATCA	220441
rs556652901	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861752	GGAAGCTGGCATGTG[C/G]AGAGATCACATGGTG	220441
rs556737016	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865447	AAAATTAAATATAAA[A/G]CTCTAAGCAGTGATT	220441
rs556738589	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61862319	AAAATTCTCATTCCC[A/G]TTTCACACACGAGGA	220441
rs556740659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855560	CGCAGTAGAAGCCAC[A/G]TGCAGTGCATCTGGT	220441
rs556752847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880706	TTCCATGTCATTTTG[C/T]AAAACATTATTAATA	220441
rs556759333	snp	A/G	0.00914312	0.0669923	intron-variant	RNF152	GRCh38.p7	18:61820308	CACTCCAGCCTGGGT[A/G]ACAGAGAGAGACTCC	220441
rs556847228	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61822716	GTGGAGTTGTGGCCT[A/G]AGCTGATATTGATTA	220441
rs556952733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891708	TGCTAGTGTCACCTA[C/T]GTTTTTAAAGTCACC	220441
rs556956372	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876432	TTAGCTGACAATGAA[G/T]TTGAGAAAGTACACT	220441
rs556971008	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858676	TCTTACTGAAATCCT[G/T]CATCCTAGCCTAAAA	220441
rs556996101	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814113	GTTGAATTCTCATGC[C/G]AATTAGCAGTATTAG	220441
rs557107110	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833780	TGACAACAATTTGAA[C/G]AGATTTTTCTTTCTG	220441
rs557114430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839469	ACCTTGGTTTTTACT[C/T]TTATTTTAGAGAGGA	220441
rs557149198	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844407	AGGAGTTATGAGTAA[A/C]AGACTATTGGAAAAT	220441
rs557214006	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876949	AAGAGACTTGACCAT[G/T]GTATCCTCAAGCCAG	220441
rs557262609	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870705	TTCCTACTATGGTTT[A/G]TGGACCTCATTTCTT	220441
rs557282520	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882526	AGAACTGGCAACCAA[A/C]AAACTAATCACTGTT	220441
rs557331863	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829001	TACCATTTCAATGTC[A/G]AGGGTGAGGACTCAG	220441
rs557384999	snp	C/T			downstream-variant-500B	RNF152	GRCh38.p7	18:61807617	TTTTTATCAAAAAAG[C/T]CTCTCCAAAATACCC	220441
rs557428353	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832453	TGGTAAAAACTGCTA[G/T]CCTAATTCAGTAAGA	220441
rs557500674	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807668	GAAGGACACCTTTCC[A/G]GGCTCAGGGCCAAGA	220441
rs557523690	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61869426	CCTGCACCTGACAAG[A/G]GATTCTGTTACTGGA	220441
rs557524771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839634	GGCACGGTGGCTCAC[C/T]CCTGTAATCCCAGCA	220441
rs557527611	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61870524	CCTGCCGACTCTGTG[A/G]TTCCAAAGCCTGCTA	220441
rs557560165	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809203	GCTTCATGTCTCCCT[G/T]TCCCTCTCCCTCTCC	220441
rs557586248	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61826048	CTTTCACAGATACTC[A/C]ACTCTGCCATCAAAA	220441
rs557638574	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853745	GTGATTACATTGGGC[C/T]CAACCAGATATTTCA	220441
rs557663998	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846241	CTTGCCTTTTCCTCA[A/G]TCTTTTCTTTCTTTT	220441
rs557747292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889727	CACATTCCTGCCCCC[C/T]TCAGATCTTATCTGT	220441
rs557773541	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858632	CCACCAAGCCAGTCC[A/G]CAGTACTCATTCCTA	220441
rs557786797	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61838747	TGCTGTTCAAAGTGC[A/G]ACTGCAGGCCCAGCT	220441
rs557941538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850557	ACTGATAAATTTCAA[A/G]TTACTGAGAGGCAGA	220441
rs557991864	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811119	ATTGATGAGTTCTAG[-/A]AAAAAAAAATCAACC	220441
rs558040846	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845868	TCTCCCCAAAATGCA[C/T]ATGTTGAAACCTAAT	220441
rs558085048	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61886089	GTTAGAATCATGACC[C/G]TCATTGAGAACATTC	220441
rs558122243	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61846016	ATCTCGTTCCACCAT[A/G]TGAGGACACAGCAGA	220441
rs558162306	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61872194	GTGAGAACTCTATCA[A/G]GAGAACAGCACCAAA	220441
rs558169838	in-del	-/TTTTTTTT			intron-variant	RNF152	GRCh38.p7	18:61886006	TTTTTTTTTTTTTTT[-/TTTTTTTT]GTGGGCAAAGTAGGA	220441
rs558178670	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61844252	GGGAGGGGAGGGCAG[A/G]CCCCATAGTATCTAG	220441
rs558185557	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61833434	CAATGCCCCACTGCT[A/T]CAGCTGCAAATCCAA	220441
rs558185822	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61831470	TAACGCCAGGATGAA[A/C]ATGCTTCCTGCTCTT	220441
rs558205459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854824	CCAAGCTTATATTTC[A/G]CCTATGTCTGTGTTC	220441
rs558241198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850960	ATGTTTGCTTTCATA[C/T]ATGATTGGCTGTGTA	220441
rs558264627	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812174	CAGCCACTAGACACA[A/T]AGGGCTATTTAAATT	220441
rs558303401	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809401	CTCTATTTCCTTCTG[C/T]TTACAGCCCATGCTC	220441
rs558321185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849957	CATTCTCAGTGCTTA[C/T]TGCCTATCTCTAAGA	220441
rs558362322	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61825392	GCCTGTCAGAGCCAG[A/C]AAGGACATTTGGAAT	220441
rs558410597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879894	CGCTTGAACCCAGGA[A/G]GCAGAGGTTGCAGTG	220441
rs558425593	in-del	-/CTAA	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61833301	TCAGAAAATAATTCT[-/CTAA]CTAATACTCTCAAGT	220441
rs558435093	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844504	GGTGGAAAAAGCCAC[A/C]CTGGCTCTGGTGGGT	220441
rs558468015	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864231	TTTCAGACACCAAGC[A/G]TAAGTCCCAGGCCTC	220441
rs558481038	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833972	GTTAGCAAAAGCTAA[C/T]GCAAAACTGCTCTTT	220441
rs558491828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867683	AACTCTCCACATCGC[C/T]GGCCTCACCATCCTG	220441
rs558508501	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61838527	AATGGACCTCAGTGT[A/G]AGCTTAAACCAACCC	220441
rs558596334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847390	TCTAAAAAGAGGTTT[A/G]GTATTGTTACAGTCA	220441
rs558611231	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61873508	GCCTGGCTAATTTTG[C/T]ATTTCTAGTAGAGAT	220441
rs558868278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860078	AAGGAGAGACAGCCA[C/T]GTGATGACAGGAGCC	220441
rs558876840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61884372	AAGGCAGGCATATAT[A/G]CTAAGGTATCAAGAA	220441
rs558883608	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869246	TTTCAACTGCTAACT[C/G/T]CACAAAATCACTAGG	220441
rs558904474	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832026	AAACTAAGAGACACA[A/G]TTCCTAAGCCTTGAA	220441
rs558930974	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865527	CAGCACAAAAAACGC[A/C]ATACTATTTGTCCCC	220441
rs559023185	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812180	CTAGACACATAGGGC[C/T]ATTTAAATTTAAGCT	220441
rs559056381	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61835389	AGGTTATATTGTTAC[A/G]TGAAAGAGTTCACCT	220441
rs559092922	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833736	CTGAAGCTGGATTAT[A/G]ATAAGCAGATAAAGA	220441
rs559101723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877807	CTACCAGGAATACTG[A/G]CACGGCTGCTTCAGC	220441
rs559134656	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878204	CTAGGGGTAATTTTG[C/T]CCCCTAGAGGACATT	220441
rs559139209	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61892409	CAATCAGCCTTCCAA[C/T]GATACCTTTTCAACA	220441
rs559154407	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814966	GAGACTTGACTCATT[C/G]ATGCCCAATGAAGTC	220441
rs559156442	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821397	CTGCATTCCAGTTTA[C/T]TTTCTGGAGCGTAAT	220441
rs559162304	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815275	GAGACACTTGTTCAA[A/T]TATTTCCTCCAAATA	220441
rs559200395	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808748	TTTTCCCAACAGTAC[C/T]GACATACTCAAGTCA	220441
rs559263654	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814253	ATTGTCTTGACCTCA[C/T]AGGGCTATTTTCTAG	220441
rs559420589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869779	CACATGCACACACCC[A/G]GAAGCTTATCATCTT	220441
rs559425971	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61832596	ACTTATCTTTCTCAG[A/G]ATAGTCATGAAAAGT	220441
rs559431596	in-del	-/TTTG			intron-variant	RNF152	GRCh38.p7	18:61873338	GCAGTCTCCTTTCTT[-/TTTG]TTTGTTTGTTTTTTG	220441
rs559469176	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876286	TGCATCCCTTTGTAC[A/C/G]CATGTTCTTACTCCT	220441
rs559488201	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890247	CTAGACCAGATCCCT[A/G]TGGAAGTCACTAGTG	220441
rs559495005	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61872409	TAGAGCAACAGGCTA[A/G]AGACTAACAATGCTT	220441
rs559513678	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846699	AAAGGTATTCTGTAC[A/C]TTCTGGGAAATTCAT	220441
rs559524302	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859653	GGAGGCCGAGGCGGG[A/C]AGATCACTTGAAGTC	220441
rs559532184	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839691	ACAAGGTCGGGAGAT[A/C]GAGATCATCCTGGCT	220441
rs559547502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890828	CAACAATGTAAGGAC[C/T]GAACTGTATGGAATT	220441
rs559569315	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876616	ACAGCATCAATGCTG[A/G]AGACGTCTTGACTGG	220441
rs559636698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872411	GAGCAACAGGCTAGA[A/G]ACTAACAATGCTTGT	220441
rs559711724	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852624	CTGCAGTGAGTCTCA[A/C]CTTAGCTGCAAACTT	220441
rs559739886	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861840	CTAATAGAGTGAGAA[C/G]TCACTCACCAACCCA	220441
rs559754582	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811128	TTCTAGAAAAAAAAA[A/T]TCAACCCATTTCTGC	220441
rs559765196	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831630	TAAAAAAAATAAGCA[A/C]TTTAGAACACAATGC	220441
rs559768538	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61829193	GCAGGTGGTTTAGCT[C/G]TTCTCCTAGCGAATA	220441
rs559851405	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61867930	TACAACTTTACTATT[A/G]TGTAAATTTAACCTT	220441
rs559895304	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824982	AGCAAATAAAGATGA[A/T]CAATTACCCTGACTG	220441
rs559911190	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858098	GCAGCCACATGCAAA[C/T]CCTCTACCCCAATTT	220441
rs559932325	in-del	-/ATAT			intron-variant	RNF152	GRCh38.p7	18:61827597	CAGTGGGTTTTATAG[-/ATAT]ATATCTCTTTAAGTA	220441
rs559957297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858256	GCTTTCTTGATTCCT[C/T]AGCTCTTTGAATCTG	220441
rs559969991	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810579	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	220441
rs559970937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845310	TGCTGTGTAAGAAGA[A/G]CAATGCTAGGGATCT	220441
rs559978204	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61862509	GGATCCCACCCTGTG[C/T]CCTGGGGACAGGAAT	220441
rs560042978	snp	A/G	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61882320	TATTAGATGCATTCT[A/G]TTTGCCTATAAAATT	220441
rs560061584	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61874778	GGGGTATCTAATCCC[A/G]GTCTGGTTCTTAGCT	220441
rs560075762	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61855614	CAGCACCTGTGCCAG[C/T]GCCTGGAGCTGCCTG	220441
rs560111672	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61819952	CTTAAACCCGGGAGG[C/T]GGAGATTGCAGTGAG	220441
rs560150931	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855680	AGTGGCTGGACCCCA[A/C]ACTCGCTCACCACAC	220441
rs560190341	snp	C/T	0.0023933	0.0345097	intron-variant	RNF152	GRCh38.p7	18:61873735	AGTGAACTCTAATTG[C/T]TCAAAAGTCCGTTAT	220441
rs560191925	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB, nc-transcript-variant	RNF152, LOC105372159	GRCh38.p7	18:61894569	GCCCGGGACTTCTCT[C/G]CGTCAGTCCCGAATC	220441
rs560198651	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829331	GAGGAGGCACAGACC[A/C]AGAGACAGATGGGGG	220441
rs560235677	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815515	GAAGGTCACATTGTA[C/T]GCACTTGTACAGTTT	220441
rs560259547	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895718	TTGGCCAGGCTGGTC[C/T]CGAACTCCTGACCTC	220441
rs560269278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847702	CGGGTTTCTCATAGG[C/T]GTCTCAAAGCTAAGA	220441
rs560277654	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61849646	TCCAAAACAAAATGG[A/G]TCTCTCCTCTACCAA	220441
rs560347830	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810987	GTATCACTCCTTTTG[C/T]ACCGATAACTTTTGA	220441
rs560355394	in-del	-/GT	0.260633	0.249774	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810276	GCTAAATCGTGGTGT[-/GT]GTGTGTGTGTGTGTG	220441
rs560420990	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61841798	GCAGTAAATCACTAA[A/T]CCTGCTTTCAGTGGC	220441
rs560429983	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854211	CTGCTTCTCAGCCAA[C/T]GCACAGCAAATGGAA	220441
rs560435911	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879493	TATATATGGTACTTA[C/T]AGCTTTCCATCACTA	220441
rs560455369	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61888204	CCTTAGCAGCCAAAC[A/G]TGATCTAGGCCAAGA	220441
rs560470792	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810385	GTGCAGTGGCCCATG[A/C]CTGTAATCCCAGCAC	220441
rs560499086	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61863946	GGCTGCCTTTTCCAT[A/G]TATTTTAATCTTTCT	220441
rs560501850	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893279	GTCATATGGGAATGC[A/G]GGGCGCCTAGTCAGC	220441
rs560523836	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854943	GAACTACAGATAACT[A/C]ACAGACTGTCTCAAA	220441
rs560529726	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873222	GAATTTCACAAAATG[C/T]TTAAAAGTTAATTAT	220441
rs560538009	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837258	ATTTTAAGAGACTAC[A/G]GAGATGAGGAAACCA	220441
rs560553668	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61867081	CCTAGATGCTCGCCA[G/T]CTGAAGTAGGAAGAA	220441
rs560554503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828705	TCCAACTTCTTATTC[A/G]TATTTCCCAGAGAAA	220441
rs560706397	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61853545	GATCTGCCAGCCTTG[C/G]CCTCCCAAAGTGCCG	220441
rs560731841	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880990	GCAATCTCAGCTCAC[C/T]GCAACCTCCGCCTCT	220441
rs560741074	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61879967	CGAAACTCCATCTCA[-/A]AAAAAAAAAAAAAAT	220441
rs560758277	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61886296	TCGTTTTCTGTGTTG[C/T]CAAAGAGTCACCAAT	220441
rs560880475	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809734	CTAAAAATATCATAG[C/T]ATGAATAATATAAAA	220441
rs560883590	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61861791	AGCAAGGGTGAGGAG[A/G]CAGGCTCTTTGTAAC	220441
rs560902775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822280	ATAACCTCATAAAAC[A/G]GTACATAGTTACATA	220441
rs561041114	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834862	TTAAACTAGTACTTC[C/T]ACAAAATAATCTGAA	220441
rs561051015	snp	A/C/T	3.29942e-05	0.00406155	missense	RNF152	GRCh38.p7	18:61816226	AAGTGTGTGGAATGG[A/C/T]GATGACAGCCAGGAC	220441
rs561052830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855082	GGCTTGTGTTCATGC[C/T]AAAGCTGTGCTCTGA	220441
rs561077035	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61829639	GGCGGTTGAAGGGGA[C/G]TGAAGAGGGGAGGAC	220441
rs561078640	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814913	GTGTAGGAGACCACT[C/T]GCTGGGTCAAGATGT	220441
rs561081224	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818372	AGGCTGCAGTGAGCC[A/G]TGTTTGCACCACTGC	220441
rs561084347	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848503	ATAGCAAGCAACATC[C/T]GTAAACTTACTACAC	220441
rs561099306	snp	C/T	3.69058e-05	0.00429553	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816491	GCAGGAAGGGCAAGG[C/T]CAAGGTGAAGGGGAA	220441
rs561149905	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855634	GGAGCTGCCTGCCCC[A/G]CTGCAGCCCCTGGTG	220441
rs561162033	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810156	CATAATGTATGCAGC[C/T]CATAGCAACAGTTAA	220441
rs561184722	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810237	ACTAATAACAGTTTT[C/T]TACTGAATTTTAACT	220441
rs561186018	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812656	AATTCATGCTTCTTA[C/T]AGTTTACTATTTATA	220441
rs561196658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846966	GAGTATCTGCTTCTT[C/T]ATGTGTAACTCAGGG	220441
rs561233312	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810681	TAAATAAGTGTCTCA[C/T]GTTGAACAAAATCCA	220441
rs561261955	snp	A/G	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61861760	GCATGTGCAGAGATC[A/G]CATGGTGAGAGAGGA	220441
rs561300004	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885599	AGGCGTGAGCCACCA[C/T]GCCCAGCCGAGAGCG	220441
rs561300225	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841091	GCAGTTCATGGGGAA[A/G]CTGATCAGAAGTCAG	220441
rs561305495	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61808057	GGGAAAAAACCAATA[A/C]GTGAGTCTATTTGAA	220441
rs561481282	snp	A/C/T			intron-variant	RNF152	GRCh38.p7	18:61850130	AGTGTTGAAAAGACA[A/C/T]GAGTCTGGAATCAAA	220441
rs561549542	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61817457	TTTTTGAATAGATAC[A/G]GTCAGCCCTTTCTAT	220441
rs561577283	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892672	GGAGTTTTAGCAGCC[A/C]CCACACCTTCTCACA	220441
rs561602975	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808935	GGGGACTCCTTGGAC[C/T]CTCATGAGCTGAGCA	220441
rs561603428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851300	TGAAGTCCTTCACAA[A/G]GGTGTCCACTCTGCA	220441
rs561637663	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61884704	AGCTAGGATTACAGG[C/T]GCCCACCACCATGCC	220441
rs561638667	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61857129	CACTTTTTACTTTGT[A/G]CTGATAATTCCTACC	220441
rs561654347	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811226	TTGAAACAACATAAG[C/T]TTTCAAATAAAGGGA	220441
rs561690253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844458	ACTATGCTTCACCTT[A/G]GCAAAAGAAAACCAT	220441
rs561728232	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883285	GTACCGGGCCCCAAG[A/C/T]GGCTACCCCTTTTTA	220441
rs561748160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882589	AGAGCACAAAGGGTT[C/T]TCATTTGAGGCATCA	220441
rs561765303	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873755	AAGTCCGTTATGAAC[A/G]TCAGTTTACCTGACA	220441
rs561795568	in-del	-/T	0.26078	0.249767	intron-variant	RNF152	GRCh38.p7	18:61853297	TCTGGTTCCTTGCCC[-/T]TTTTTTTTTTTTTTT	220441
rs561812168	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863191	CTGCAATCCCAGCAT[G/T]TGGAAGGCCGAGGCA	220441
rs561872496	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882082	TCAGAAACTTTTTGA[A/G]TGCAAACATGACACT	220441
rs561878006	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837294	AATTCATGAACCACA[A/G]TGAGATCCAGGATTG	220441
rs561899232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61838023	TTTTGAAGAAACACA[C/T]ACATGGTTCCTCTGA	220441
rs561913586	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835829	TTGATACTAGTATAG[C/T]AGTAATTCTGAAACT	220441
rs561941707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823560	CGTCTCAGCCTCTCA[A/G]AGTGCTGGGATCACA	220441
rs562030431	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887278	CTAAGAGTGACAGCA[C/T]TTTCCAAACTGGAGT	220441
rs562086905	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61887854	GAGCCGGGAAAGTTA[C/T]ACTTCCTTGGTAGGT	220441
rs562121253	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61870125	ATTTGAAAACATGGA[A/G]ATATTACGTTCCTGC	220441
rs562149501	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880827	TGAATTTTGAAAATA[C/G]CATACACCTACACAA	220441
rs562162118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856292	AGCTGGAAAATGACA[C/T]GGGGAAATACACGAT	220441
rs562205810	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61842475	GAGTTGTCACAGGGG[C/T]TTTGTTTCCCTGGAG	220441
rs562228043	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61868556	AAAACTACAAAAATT[A/G]GCCGGGCGTCATGGC	220441
rs562266627	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869201	CCTAATTAGTAAAAT[C/T]CAAAGAAATAGGGAA	220441
rs562370900	snp	G/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61836413	GAGGTAGGGCCTTCA[G/T]GAGGTAATTAGGTTT	220441
rs562378379	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61881646	GAATCCAAAATTGAT[C/T]ATCACTGTCTTCCTA	220441
rs562382802	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61828135	AAGATATTTCCGCCA[A/C]CCCGAAAGGTCCCCT	220441
rs562392456	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895917	TCTTGTCATGTCCCA[A/C]AATTACGACCTGTTG	220441
rs562396839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857003	CCCAGGGCAACATTT[C/T]AAATTAATTAAGTAG	220441
rs562482829	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850591	AAGCTCCATATACTT[G/T]ATTAGAGCACAATAA	220441
rs562554360	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864146	CCAGAATTCAATTCC[A/G]TTTTGACCCTAACTA	220441
rs562593565	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815616	CATGATTATGAGGAT[A/G]CATGCAATCATCTTC	220441
rs562679990	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843797	ATCATGGTTGCCAGG[A/G]AATGGGGAAAGAGGA	220441
rs562711447	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886530	TGTTACATGATTTTG[A/C]CCCCATTGTAGGCTA	220441
rs562725788	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841846	GTCAATACATTCTTT[A/G]CACAGGGACAGATGG	220441
rs562741776	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829489	CCCAGGGAGAGAGGA[A/G]AGAGGGGAGAGAGAG	220441
rs562748888	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811676	GCTCTTATATTTGCA[C/G]CTTACTAATACAGCA	220441
rs562888689	snp	G/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61848363	TATGCCACATTTTTT[G/T]AATGATTCCATAGCC	220441
rs562925869	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61839524	TAATGTTCCCACTCC[A/G]TCCTAGCAGGTGGTT	220441
rs562928993	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854958	CACAGACTGTCTCAA[A/C]TGCTACAAAATACCA	220441
rs562934604	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887178	GGAAAACTTGAAAAG[C/G]AAAACTGAAGAATAT	220441
rs562962662	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819441	GGAAAGACCTATTGG[C/G]AGGCTATTACATTAG	220441
rs563069189	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864517	TTCACCGACCAGAAC[C/T]CTGTCACTTAGGGGT	220441
rs563082271	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61817943	AAAGAATTACTCAAC[A/C]ACTATTGCAGAAAAA	220441
rs563112674	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61890786	AAACAACTCTGAGGG[A/C]ATTAGAAATGAAAAC	220441
rs563168348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827082	CATAATGATAGCTCC[A/G]GATTAAAGGTAATTC	220441
rs563171127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880113	AAACAATTCACACCA[C/T]CTGACTTCACAGAAA	220441
rs563243076	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833322	AATACTCTCAAGTTA[C/T]TGAGTAACTTAAAAT	220441
rs563251149	snp	G/T	0.00398564	0.0444627	intron-variant	RNF152	GRCh38.p7	18:61845922	GTGGGGCTTTGTGTG[G/T]GGGGGCGTGGTGATG	220441
rs563273027	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61839205	AAATCTACTTTGGTA[A/C]ACTACCTCAGATCTC	220441
rs563394657	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809577	GGCTACTAGCCCTAC[A/C]TCCCATGGAAATAAA	220441
rs563436941	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61882053	AAACATCCGAAATCC[A/G]AAATGCTCCAAAATC	220441
rs563446433	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61870890	TGCACCCATGATTCC[A/G]TCCCCCAAATCAGTT	220441
rs563500059	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865195	TGCAGCCAAATTGTC[C/T]GGCACATATACTTGG	220441
rs563520822	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825680	CTGAGAGTTGTGCCT[C/T]AGGGACTGCAAGGGC	220441
rs563642828	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837927	GGATCCAACAAAATC[C/G]AGGCCTCATCTCCTG	220441
rs563660079	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846855	AGCTTTGCTTGAGCT[A/G]TGGAGACTCCAGAGC	220441
rs563660181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824408	ATGGCAGTACTGCCA[A/G]GCCACTTATTCTATG	220441
rs563672468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831564	TGTGAGGTTATGGAT[C/T]ATTCATACTTTTATA	220441
rs563682700	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867846	AAAATGGCCACGAAT[A/G]TCCAGTGCACACTAA	220441
rs563698855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824830	TGCTCTAATCACTCA[A/G]TGACAGTCAAGAAAA	220441
rs563704020	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61869755	TGGGCACACACACAC[A/G]CACGCACACACATGC	220441
rs563777331	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61837157	TCAGTCATGACAGGG[A/T]TGATGAGACATGTAG	220441
rs563785063	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830788	GAAAAGATCCCTGAT[C/T]TCTCAGTGAGGCAGC	220441
rs563820331	snp	G/T	0.0123036	0.0774623	intron-variant	RNF152	GRCh38.p7	18:61844138	AAAGAAAGAAAGAAA[G/T]AAATTAAGAGAAAAG	220441
rs563890440	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851407	GGAAAAGAGGAGAAA[A/C]CACTTACCCAAGCGC	220441
rs563890494	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858154	AGACATTTAGGTAGT[A/T]TGGTATAACTCTCTG	220441
rs563909897	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883408	ATAATAAATATCCCA[C/T]TCCAAAAAGCAGATT	220441
rs563999863	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863719	CTGATTCTGGGCTTC[A/G]AAGAGTGCTTGAGAG	220441
rs564012650	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61838121	TCAGTCCCTATGAAA[C/T]AATTCCCAAGCTGCA	220441
rs564022156	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818685	AAAGCACAAAGCTAA[A/C]TACTGTAGGATATAA	220441
rs564041688	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61889484	ACTGCTGAATCCAGA[C/G]CACCTTGCAATGCCT	220441
rs564059489	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61879402	GCATATCATATCAGG[G/T]ACTTGAGCATGCATG	220441
rs564153457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61822735	TGATATTGATTACAT[C/T]GGGCTGACCTTGAAG	220441
rs564262931	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876740	GACATTAATAGAACC[A/G]TCTACTCTACCCCGT	220441
rs564276233	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893774	CACCCAGGGGCGCGC[G/T]CGGCGCGGGCACGAG	220441
rs564297065	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817980	AGTCCTAGAACCCCA[A/C]CAACACCTAGAGATG	220441
rs564312113	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870367	CATGTCTGATGCATT[G/T]CCTGTCCTCATCTCC	220441
rs564318793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830148	TGCCTCAGACTCCCG[A/G]GTAGCTGGGACTACA	220441
rs564497541	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61878656	AGAAATCCAAGACCA[C/T]GGCACCAGTGGATTC	220441
rs564522113	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61843959	AATGCTCAATTTTAT[A/G]TTATGTGTATTTTAC	220441
rs564540811	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61876534	GTCATGAAAATACAG[A/G]AGATCTCAGAGAAAG	220441
rs564628612	snp	A/G	0.0126979	0.078662	intron-variant	RNF152	GRCh38.p7	18:61829981	CAGTGGCTTTAAGTC[A/G]CCATCATGTGTAGCC	220441
rs564661460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869631	AGCTGATCCAGGAGG[A/G]TGCCAGGAAGACACC	220441
rs564690610	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815685	TATCTTGTTGAGACC[A/G]CACCTTCTGCCCTTT	220441
rs564732646	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872486	GAAAATGTCTGGTTA[A/C]AAATTCAAAATTAAC	220441
rs564818644	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61824343	ACCTTCTAGTAAAAA[C/T]ATTCTATGACCTAAA	220441
rs564876106	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878414	AGTCACAGGTCCATG[C/T]TCAGGTCTAACATCA	220441
rs564895099	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827302	AGGAACATTGAATAA[A/G]TTGCCCAAACACATT	220441
rs564908481	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61827954	CCATCATTAATCCAC[A/C]TTTTCTAACCTAACA	220441
rs564948339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840318	AGCAGCCTGAATGGA[C/T]CACAGTGTCCAAAGT	220441
rs564960288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858929	ATTTGGGGTCCCCTG[A/G]CTTTGTTCTTACTGT	220441
rs565003292	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841004	CAAAACCACATATAA[A/G]TTATCTGGTTCCTAC	220441
rs565025597	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866481	CTGTGCTTTGAGCCA[A/C]CTGATCATGCCATCC	220441
rs565065410	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61874436	GAGCCCTCAATCAAC[C/T]AACCAGGACCACTGA	220441
rs565069414	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864961	GGAGGCGGAGGTTGC[A/C]GTGAGCTGAGCTCGT	220441
rs565097462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860778	ATAACAGCTCCATGC[A/G]TGTATTACCCTGAAG	220441
rs565129525	snp	A/G	3.30175e-05	0.00406296	missense	RNF152	GRCh38.p7	18:61816132	TCTCCGGGCAGCAGC[A/G]CACGCTCCTTGGAGA	220441
rs565195032	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859432	AATTGCAAGGCTAAG[C/G]GTTCCGGAGAGTCAG	220441
rs565207719	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61867684	ACTCTCCACATCGCC[A/G]GCCTCACCATCCTGG	220441
rs565216727	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866915	ACAAAAAAAACAGAC[C/T]TAGGGGCTTGTCCCA	220441
rs565224475	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846402	GCCTATGCAATCTCA[C/T]CTCATTCAATCTCAT	220441
rs565228914	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61870911	CAAATCAGTTCAGCC[A/C]AGCTGTCTAGATAAT	220441
rs565322927	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846801	AGCCAGACAATGCAA[C/T]GCACTGATATCTAGA	220441
rs565445326	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807935	CACTTAAAATCCTTG[G/T]CTCAGGATCTTCTTA	220441
rs565478758	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883649	CATGACCCAGGTATG[C/T]TCTTAGTCATGGGCA	220441
rs565530979	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852768	GGTGACTCACTGAGC[A/C]TACAAGGTTGAGACT	220441
rs565534232	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826011	TATATCCAGCTTCTA[A/G]GCTTTGCGGATCCTA	220441
rs565545519	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832257	TTCAGATGTGCACAA[A/G]TAGGAAAGTCTGTAC	220441
rs565579640	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61890938	AAGAGGCATTAAAGT[A/T]GAGGCTGGATGACCA	220441
rs565632251	snp	A/G	0.0142736	0.0832652	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813705	CAGATATCACTCACA[A/G]AATTAATCTGAATAT	220441
rs565638085	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895336	CAGGGCTCAGTTGAG[G/T]GTGATCCCCACGGAT	220441
rs565643432	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61820236	CGGGAGGCTGAGGCA[A/G]GAGAATGGTGTGAAC	220441
rs565645729	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61832755	ATAAAATCGACAGGA[C/T]TTTAAAAGCCACCCT	220441
rs565650869	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870515	CTTCAAACCCCTGCC[A/G]ACTCTGTGGTTCCAA	220441
rs565676721	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871202	TCCCACCCCCACCCA[C/G]CTCCCCCCACCCCAA	220441
rs565687619	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864721	AAGAGCCCACCAAGA[C/G]TCATCTCATTAGCAT	220441
rs565738100	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832080	ATTGTCCTTCATAAC[A/T]TCAAATGTATTCAGT	220441
rs565761308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853172	GCAGCTTAAAGCAAC[A/G]TGAATTGATTATCTT	220441
rs565780542	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889065	CCAACCCCAGGCACC[C/T]TGAATGGGTTTTTGG	220441
rs565835869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863307	AGGCGTGGTGACACA[C/T]GCCTGTAGTCCCAGC	220441
rs565860427	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61823809	GCCTGGCCCTGCCAG[A/C]ACAGCCCACTAGGTC	220441
rs565871939	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61859109	GGCTCCTACAAGTCA[A/T]CACCACCATTCAGAT	220441
rs565933493	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826567	GCATATATAAACTTT[C/T]TTTCCTCTTTACATG	220441
rs565962597	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61857760	TTCTAGTTTTGGATA[A/C]TAGCCTATCACAAAA	220441
rs565963629	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858567	CCCTGGGCCCCAACT[C/T]TACTGCAGCCCCTCC	220441
rs566019956	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61842479	TGTCACAGGGGCTTT[G/T]TTTCCCTGGAGACTT	220441
rs566039004	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889722	CTAAACACATTCCTG[C/T]CCCCTTCAGATCTTA	220441
rs566062175	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812113	ATTAATACCTTGATG[A/C]TGGATCCCCAAGCGC	220441
rs566084944	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61850934	TGGGCACACGGAAAT[A/G]CCCAGTCATCATGTT	220441
rs566112635	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61829832	GACCAGTCCCCTCCT[A/T]TTCTGTAATCTGGGT	220441
rs566114821	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893080	GGCGTCACGGCTCCT[A/G]ATTGTCTCTACAGGA	220441
rs566148422	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817767	AAAAAAGTGTTAGCA[A/T]CCTGGTATGGAGGGG	220441
rs566148673	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824481	TGATCTGGCAAGAAT[A/G]CGCATTTATGTGAGA	220441
rs566171962	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61882891	CCACACTACCATCAT[A/G]CATACAACATAGGAA	220441
rs566201265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857220	GGGAGAAAGTGCAGA[C/T]ACTTTTCTATTTTGC	220441
rs566202828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61851479	CTCAGGAACTGTGCC[C/T]AGTTTTCTCCGTGCC	220441
rs566230002	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877062	TGAATCCTGTGCAAA[C/T]AGAACAGGCACACAG	220441
rs566267837	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61865890	GGAAGGCTAGTCAGC[C/T]GAGTGTCAATTACAT	220441
rs566272418	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61828439	CAAAAAACATTTTTT[C/T]GTAGAGACGGGATCT	220441
rs566310626	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844766	CTAATGAGGGCAGTA[A/C]GATGCAATGAAACTT	220441
rs566361472	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61880378	CCCTAATCCCAGTTG[G/T]GAGTGTGGCTCACAG	220441
rs566370199	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847971	ACTCACGCTTCCCTT[C/T]GTGTGATTATTTTTC	220441
rs566408109	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892823	CGAGTCTCTTTCACC[C/T]CTTCTGCGTGATGAC	220441
rs566430289	snp	G/T	1.65002e-05	0.00287225	synonymous-codon	RNF152	GRCh38.p7	18:61816257	CTCCGGGTCGTCCGG[G/T]AGCTGCGACACGGAG	220441
rs566498771	in-del	-/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811739	GGGATTTCATTAGGC[-/T]TTTTTTTTCCTGTAA	220441
rs566504540	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809788	TCGAGCTAATGAGAT[C/G]AGTATTTCAAGCACC	220441
rs566507057	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893909	CAGGAGACACGCAAC[C/T]CCCGGGACCACCTCC	220441
rs566509519	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61840549	TCCTTGCCATACTCT[A/G]TGCATATGCTTCTAG	220441
rs566553237	snp	G/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61839548	GGTGGTTGTGTTGTA[G/T]TAACTTTGATCACCT	220441
rs566583670	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61846205	ACTTCATAATTCTCA[A/G]CCCAAACACTCTCTC	220441
rs566668825	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847031	ATTAAATGGGGGTAA[A/G]TAGCAAGGTATCCAG	220441
rs566721505	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61848537	GCCCCCCAGGCTGTA[C/G]GTGGCCTCAGCCTAA	220441
rs566826532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877628	TGCTTGTTAATCACA[C/T]GTCAAAATTATTAGG	220441
rs566873219	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831937	TGGGGGGGTGTGGGT[A/G]TGTATAGGGGTGTGT	220441
rs566906887	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61871035	GAGGCTGTTACTAGA[A/C]TTCACTAGAAGCATT	220441
rs566962156	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61892274	TCCCAGTACTCACTG[C/T]TAGCATGTCTCTCTT	220441
rs566969185	snp	A/G	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61857152	TTCCTACCCTGACTT[A/G]CATTATACGTCAGGG	220441
rs566977461	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808136	TAAAATCAACATTAC[A/C]ACATATACAAAGGAC	220441
rs566982365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882383	TTCGGTGAAGTAATA[A/G]ACTATGAAGAAATCT	220441
rs567018309	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61874392	TGTAGTTAGCATGCA[A/C]AGAGTGGAAAGAACG	220441
rs567024958	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61833951	CAACTCCTTTAATTA[C/T]GTGTGGTTAGCAAAA	220441
rs567055837	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61845233	TGGGATAATAGGCGT[A/T]AGCCACTGCACCCAC	220441
rs567062870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821034	TGTTCTCCACTTCCT[C/T]TCCACTCAGTCTAGT	220441
rs567099306	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61821745	ATTACCGCCTGAGCT[C/T]CACCTCCCGTCAGAT	220441
rs567160007	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61834408	CCTAGGAACCTTTCT[A/G]GAATGATCATATTTT	220441
rs567186791	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808552	CCCACCGCTAAAGCC[A/G]TAGGGTGGGAGGAAC	220441
rs567224203	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61893022	TGCACTAGGGAGGTG[C/G]AGCAAGGCAGATGAG	220441
rs567257738	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860369	GAGAAAATGCAGTCA[C/T]GCACCACATAACGTT	220441
rs567273718	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853955	CCTCCCTGCCCACCT[C/G]CCCATTTTTCAACTG	220441
rs567334675	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827361	TGTATGATTTCAGAC[G/T]AGTAGAACTTCATTA	220441
rs567340760	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61820322	TGACAGAGAGAGACT[C/T]CGTCTCACCAAAAAA	220441
rs567341260	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61846048	GCCCTTTATGAACCA[A/G]AAAATGGGCTCTCAC	220441
rs567379369	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820944	GCAGGGATGATGGAG[A/T]TGTGGCTGAAGGTCA	220441
rs567451520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845529	GTTTGAAATTTATAG[C/T]CAAAACAGTTGCTTC	220441
rs567495864	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871537	TAATAAACAGAAGGG[C/T]TACTGCCCTCAGCCG	220441
rs567517613	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891144	TGCTAAATGAATAAA[C/T]GAGCATTGTAGAAAG	220441
rs567556026	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61854603	TCAATTAGTCATCTT[C/T]TGAACGAGGTATTAT	220441
rs567575482	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809162	CTCTTTGGGTATATC[G/T]GCCTGTCCCTTCACA	220441
rs567595610	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61847828	CTACTCTTCCCTCTG[A/C]TTGGAATCTCTGCTC	220441
rs567818477	snp	G/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61839870	TGTGTGCTTTTGATA[G/T]GTCCCCATCATTCTT	220441
rs567844037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849886	TCAAATGAGTTTGAG[A/G]AGCACCTGGCTTCTG	220441
rs567856748	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811189	TCCATTTGGAAAACA[A/G]TGAAAAGCAGACTAA	220441
rs567860581	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61842748	GGAAGGCAAGGAGGA[A/G]CAAGTCACATCTTAT	220441
rs567865715	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833290	GCCAGTCTATTTCAG[A/G]AAATAATTCTCTAAC	220441
rs567905631	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833501	ATGGTTTTAATTGTC[A/G]AAACTCCTCTGCGTT	220441
rs567925508	snp	C/T	0.00557542	0.0525036	intron-variant	RNF152	GRCh38.p7	18:61862838	AGTTCCGAGGAGGCC[C/T]AGACTTATCATTGGT	220441
rs567928897	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880570	CAAGCGTCTAATAAA[A/C]ACTATCTACTACTAT	220441
rs567981831	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61836124	ATCTTGGTATCTAAG[C/T]AGCATTTCTCACTAA	220441
rs568083938	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61837523	ACTGCTGACTTTGTA[C/G]CAGTCTCTCCACATT	220441
rs568135668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875215	CTAATGAGTTAACCA[A/G]TTTGTATGAGAAGGG	220441
rs568166680	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61862561	TAAAAAAACCCAAGC[A/G]GACAGGGTTCAAGGA	220441
rs568191490	snp	A/C	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61822285	CTCATAAAACAGTAC[A/C]TAGTTACATAAATAA	220441
rs568243229	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823883	CTGTCTGGATGTGCC[A/G]TGGAGCCAAGGGCAT	220441
rs568257769	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835694	TCAACAACAGAACCA[C/T]ATTCAAATCCCTTTT	220441
rs568257888	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61828464	GGATCTTGCCATGTT[A/G]CCCAGGCTGAAGTGC	220441
rs568329581	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874636	GGTATATCGGAGTTT[A/C]TCAATTATAGAACAG	220441
rs568361920	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836421	GCCTTCAGGAGGTAA[C/T]TAGGTTTAGATGAGG	220441
rs568421110	snp	A/C/T	1.80419e-05	0.00300344	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816471	GTCTCCATGGTGGAC[A/C/T]GTGAGCAGGAAGGGC	220441
rs568423982	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823123	ACTGCTGCATACATG[C/T]GTAGTCCAATTGACG	220441
rs568426356	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61860171	TCCCCATGGGTCTCA[-/G]AAGTGCATGGGCCTG	220441
rs568572410	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61864727	CCACCAAGAGTCATC[G/T]CATTAGCATAAGCCA	220441
rs568582360	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835257	GCAATAGGAAAAAAA[A/T]CTAAATTCCTATCCA	220441
rs568640774	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61855807	TGAGCCCAGCAGGTA[C/T]GAGCAATACCCAGGC	220441
rs568671325	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882806	ATTACAGACTCATCA[C/T]GAAAACCCTCTGGAA	220441
rs568713715	snp	A/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894963	CCAAAGAGGCCCGAA[A/T]GGACACCCCACTACT	220441
rs568747260	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61886824	TAATACAAGACAATC[C/T]ATGACAAGTGGCCTT	220441
rs568751668	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61874547	GAGACATAACAGTTC[C/T]CATGGTTACTTTAAG	220441
rs568773558	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842111	CTGAGTTTTATTAAG[G/T]GTTCACATGTATTTT	220441
rs568822204	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894802	GGTGGGTTGGGGGGT[A/G]CCCAGTCTGTGCCTA	220441
rs568886467	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61862384	GAGGAGATGACCATC[C/T]TGAAAAGAACTTCAG	220441
rs568898584	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834521	ATGGACTCTATTGAC[A/C]TTTATTTACCTTCAT	220441
rs568925878	in-del	-/A	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61876455	GTACACTCAGCCCAC[-/A]AAAAAAAAATAAGCA	220441
rs568989688	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809882	AAAAAAAAAAAGTCA[C/T]TGGCTCGACTGAGCA	220441
rs569008515	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884773	CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA	220441
rs569043617	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859857	GCACTCCAGCCTGGA[C/T]AACAGAGACTCCACC	220441
rs569047675	snp	C/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61834043	CAATGCTTTATTAAG[C/G]ACCTACTATGTACCA	220441
rs569059941	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873389	GTTGCCCAAGCTGGG[A/G]TGCAATGGCGCTATC	220441
rs569077529	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61860549	ACCTACCATGCTGCC[A/G]GTTGCATAAGAGTCT	220441
rs569114358	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61861363	TGTGTGTTACAATTG[C/T]TTGCAGTATTCAGTA	220441
rs569154607	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61861587	CTTAGTGTCTTAGTC[A/C]ATTTAGTGTTGCTAG	220441
rs569167263	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61835292	AATCTGACTAGACTA[C/T]GTCTCTCCACCTGAT	220441
rs569183766	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61828447	ATTTTTTTGTAGAGA[C/T]GGGATCTTGCCATGT	220441
rs569206589	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840615	GGTCCCAGGGAGCCT[C/G]AGAACTAGTCCTGCA	220441
rs569212398	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836077	CTAGAAACAGTGACA[C/G]TCTAGTAACAATGAG	220441
rs569219886	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828833	GATAGGGCCCTCTCC[A/T]GCTAAGGCCGGTGGG	220441
rs569263645	snp	C/G	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61888607	GTTAAGGCAGACAAG[C/G]CTGAGCTATGATGTC	220441
rs569287168	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831984	ATACTCACACATATA[C/T]CAAATAAAATCCAAT	220441
rs569340864	snp	A/G	4.94629e-05	0.00497283	missense	RNF152	GRCh38.p7	18:61816039	GGAGCCCCACCTTGC[A/G]GAGGCTGCTGTTCAG	220441
rs569381352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885780	GGGAGGTAAAACAGA[C/T]GTATATCACAAAGGT	220441
rs569422605	snp	A/G	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61822497	GGTGTGACAAAGTGC[A/G]CGCATTCATTTGGTA	220441
rs569429533	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61866795	TTTCCCCTACTTGCC[C/T]GCTGTCCCCACCGCT	220441
rs569436086	in-del	-/TCTA	0.00318978	0.0398085	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810856	TCAAGGAACAGCTTC[-/TCTA]TCTAAGTCAGGGATG	220441
rs569450404	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61821869	CTAATGCCTGATGAT[C/T]TGAGGTGGAACAGTT	220441
rs569509494	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61889690	TCAAAGTAACAAAAG[G/T]GTGACCCAAGGTTAC	220441
rs569615453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825944	AATATTTTCCCATTA[C/T]ATTTTATCTATGTCA	220441
rs569798002	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857865	ATTCAAGAGCATTTT[C/T]CAAAATAACACATTT	220441
rs569832944	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812977	AAGACACTGCAGTGC[A/G]AAGTTCATATCCCCC	220441
rs569942502	snp	A/G	0	0	intron-variant	RNF152	GRCh38.p7	18:61818899	CCTAGAGATGGGAGC[A/G]CTAAGTACTTAGACA	220441
rs569943628	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870465	AGACCACGCCTGTCA[A/C]CTTACCTACTAGCTT	220441
rs570001079	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61868462	GCCTGTAATCCCAGC[A/G]CTTTGAGAGGCCAAG	220441
rs570025287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823293	AAAGTGAAAATTGTC[A/G]TTTAAACATGTTTTT	220441
rs570031721	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61817546	AAGCCCCTGTATACC[A/G]AGGGCCATCTTTTCA	220441
rs570065978	snp	C/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61856616	TGTTTAGATTTGATA[C/T]CCCTTCTTTCTGCTG	220441
rs570111910	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61868813	TGTGCCTTGTAGTTA[G/T]GTGGCAGAAAGACAG	220441
rs570217532	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61888982	TTGGGGCTTCCCAAA[A/T]ATAGTTCAAGACTAG	220441
rs570267313	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61812045	ATGTTTTGCCTTTTG[C/T]CAACTGCATGTCACT	220441
rs570279811	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863365	ACTTGAACCTGGGAA[A/G]TGGAGGTTGCAGTGA	220441
rs570311785	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837602	TATCTGCATCCCCAT[A/G]TAACAAAATCCCTCA	220441
rs570346763	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61855477	GTGACACCCCCTTTG[C/G]GGCTCTGCAATTCCT	220441
rs570356370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857188	GCTCTGTCTCCATTA[C/T]CCCCAACACTGTAAC	220441
rs570388398	snp	C/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61850919	TGGCTAGTGCAGCTC[C/T]GGGCACACGGAAATG	220441
rs570423763	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831906	AAATAATATTATAAA[A/T]ATAGTATTATGTGTG	220441
rs570432344	snp	C/T	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61881843	GACATATTCTTATTT[C/T]CTTCTCAGAGAAGAC	220441
rs570489143	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61843476	AAAAAATTGAAAGCA[C/G]GGTCTTGATGAGATA	220441
rs570502275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844109	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	220441
rs570544454	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825139	AGTAAGCAGATATTT[A/T]TTGTGAACTCACCTT	220441
rs570614413	snp	G/T	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61818194	TTGGGAGGCCGAGGA[G/T]GGGGAATCGTTTGAG	220441
rs570650302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876183	ACTGTCTACCCTTCA[C/T]GGGCATTGTCAAATA	220441
rs570664059	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811274	AAAATCTAGACTGGA[A/G]TAAATACCAGATTAT	220441
rs570747350	in-del	-/TGCACTCCA	0.00636936	0.0560724	intron-variant	RNF152	GRCh38.p7	18:61887663	GAGATCATGCCCCAC[-/TGCACTCCA]TGCACTCCAGCCTGG	220441
rs570749536	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61863227	ATCAGCAGGTCAGGA[A/G]ATCAAGACCATCCTG	220441
rs570786483	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823645	ACAGGGAATAGGGCA[C/G]GCGATGCTGACAGTG	220441
rs570816266	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61823238	AGTTTCCTCCTATGA[C/G]CATCCTGGTTTGCTG	220441
rs570829200	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61829043	GCACAGAGACCAAGA[C/T]GAGGGGAGGCAGTGC	220441
rs570873643	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61874049	CTTCATACTATAATA[A/C]GTGTACTTTGTCTAA	220441
rs570896660	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61859512	CTGGAAGCTGCAGAG[A/C]AAAGGAGCATCACCC	220441
rs570907347	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873976	CCTTGCATCCTCTAA[A/T]GTATTTTCCTAATCT	220441
rs570928662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835992	TGTACTGAATTTAAA[C/T]TGGAACCATCAGATT	220441
rs570962763	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61839820	GAATGGCATGAACCC[A/G]GGAGGCAGAGCTTGC	220441
rs571008434	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896273	TGTGTTGCCCAGGCT[A/G]GAGTGTAGTGGCCAA	220441
rs571010553	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895657	GGCCCGCACCACCAC[A/G]TCCTGCTAATTTTTG	220441
rs571060472	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808468	CATCAAGGATTTGAG[G/T]TAATAGCCTCTGAGC	220441
rs571120200	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61842686	AAAAGAAAGAGGTTT[A/G]ATGGACTCACAGTTC	220441
rs571144893	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61820283	GCAATGAGCAGAGAT[C/G]GCACCACTGCACTCC	220441
rs571158320	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61824263	TTAAGCAAATAACCT[A/C]TAGATGAGCCTCCTA	220441
rs571227744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866020	TAAAATTTCTCTCAG[A/G]TCTATTCCTCCCACT	220441
rs571248640	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820780	CTTAACTTCTACATC[A/T]CAATGTGGGAAGTAG	220441
rs571265698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826643	AAGAACTTTCCCTCC[A/G]CAACAGTTCTAATAA	220441
rs571295318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61826078	ATGTGAAAGCAGTCA[C/T]AGTATCTCAAGGAAT	220441
rs571337805	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61833428	GATTCACAATGCCCC[A/G]CTGCTACAGCTGCAA	220441
rs571404010	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61857829	AAAGTAAATTTGTCA[C/T]TGGCGTGTATAAACA	220441
rs571440380	snp	A/G	0.00358779	0.0422022	intron-variant	RNF152	GRCh38.p7	18:61858338	ATCTCCCCTGGAACC[A/G]TATACCCTAGGATGA	220441
rs571477617	snp	C/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61883910	ACTGAAAGCTTTACA[C/G]ACTTTCAAACCAAAG	220441
rs571540940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877458	CACATCTGTCACTGT[C/T]CCCAAAAAATGTTAA	220441
rs571557255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61859752	GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT	220441
rs571573236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852202	CCTCCAAACTGGAAA[C/T]ATAAGGACATAAGAC	220441
rs571595137	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853871	TTCCAAGGATGAGGA[C/T]AAGGACTTCTCTGGG	220441
rs571599716	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61889820	TTTTCTACCCTGGGC[A/G]GTTCCAAACAAACTC	220441
rs571624763	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813618	GTCTATATCTAACCT[A/G]CTTTAACAAGTAGAA	220441
rs571674741	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811868	TTTTTGGACAATAGG[C/T]TAACATGCAGCTAAT	220441
rs571776107	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824678	ATGAAGAAAGATATT[C/T]CTATTACCCAAACTT	220441
rs571786808	snp	C/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61853580	TACAGGCTGAGCCAT[C/G]GCACCTCACCGGTTC	220441
rs571813287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61818451	AACAAAAAACAAAAA[A/G]CAAGAAAAAGCAAAC	220441
rs571852007	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870564	CCTCTTGGCCAAGCA[A/T]GAACTCTGAAAGCTA	220441
rs571857365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833001	TTGTCAAAGCAGAAG[A/G]AACAGTAAGGCATAC	220441
rs571857382	snp	C/T	0.00795532	0.062565	intron-variant	RNF152	GRCh38.p7	18:61839757	AAAAATTGCTGGGCG[C/T]GGTGGTGGGTGCCTG	220441
rs571929040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845718	AGGAACTGACCTCCC[A/G]TAGCAGAGGCAGCCC	220441
rs571976783	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857485	AGCAAATTTTCAAAA[C/G]CCATAAAAATGGCTT	220441
rs571979638	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61889842	AACAAACTCAGGAAG[C/G]CTTAAACAAGAGGCA	220441
rs571986864	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61860579	TAGCACACACAATCA[C/T]GTACAGTACACAATA	220441
rs572008125	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61879642	GGGGTCAGGAAGAAA[A/C]AGTAACTAGAGAGGG	220441
rs572027830	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886489	CTACATGAGATATTT[A/G]ATGCTTTAATACAAA	220441
rs572038336	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61863795	CAAATCTCTTCCCCA[A/G]AGCAACACCTGACAA	220441
rs572045592	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844975	ATTCCTTCCATTCCT[C/G]CTGAGGGCCATAAGT	220441
rs572133596	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866749	ATTGGTGGTGACACC[A/G]GGGGTGTGACCTCAA	220441
rs572162856	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895595	ACCTCCAACTTCCGG[A/G]TTCAAGCGATTCTCC	220441
rs572200549	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837227	AGGAAAACAAAAAGC[A/G]ACGAGATTGTTCTAG	220441
rs572224552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61887902	AGGGGAGAGGAGGTT[A/G]TAGAAAGAGAAAATA	220441
rs572244475	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61851864	GAATATAATAAACTT[A/T]TTCTACAGGCTTTCT	220441
rs572251994	snp	C/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61882616	ATCAGCTAAATACTA[C/G]AAGAACTGGTGGCTT	220441
rs572284351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824193	AATCATTACTATTAG[A/G]AATCAGGAGATAAGG	220441
rs572303492	snp	A/C/G			intron-variant	RNF152	GRCh38.p7	18:61870193	TAAAGAAGCTGTGTC[A/C/G]GGATGGGGGTGTGGA	220441
rs572312755	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61883265	CTTTACTGAGTGTCT[A/G]CTGTGTACCGGGCCC	220441
rs572445245	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881463	TGGGAAGAGGAGAAG[G/T]GCAGATGGCAGGCAA	220441
rs572446653	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856827	CTCACTGAAGTGGGA[A/G]AGCCCAGGAAAAAAG	220441
rs572456982	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811568	GTTTGGCATCTGAAA[A/C]ATGATGCCCACATAT	220441
rs572462850	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893503	GGGATTGGGGACCGC[C/T]GCTTCCCGAGCAGCG	220441
rs572486743	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885230	CCAGAACAACACAAC[G/T]GCAAAAGAATATCAC	220441
rs572492147	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843582	GATGAATGGCAAAGC[A/C]AAATATGGTATGGCC	220441
rs572515436	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61875563	AATGACCATCTGGGC[A/G]TGGATTACCCACGAA	220441
rs572560130	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891844	ATACCAAGGTGTTAC[C/T]GCAATGTAAAAGAGA	220441
rs572624255	snp	A/G	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61884390	AAGGTATCAAGAATT[A/G]AGAGAATATCAGATA	220441
rs572629421	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61869225	TAGGGAATGTCTATC[C/T]TCAAATTTCAACTGC	220441
rs572653665	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61881934	TTCTTAAATAACTTA[C/T]TGTTTTGTTATAAGA	220441
rs572690204	in-del	-/TAC	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61872083	AGGCCTCAGGAAACT[-/TAC]AAACATGGTGGAAGG	220441
rs572718964	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61874988	CAAAGACCCACCTGC[A/G]TCACCGGCCAGCACC	220441
rs572743824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61830685	AAAGGAAAGAGGGGC[A/G]AGGCTGGAATGAAGG	220441
rs572796565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61878556	AAGATTTCTGTCTTA[A/G]TCTGTTTGTGCTGCT	220441
rs572849768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61846793	AGTAACAAAGCCAGA[C/T]AATGCAATGCACTGA	220441
rs572890092	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853998	CTCAAGGTTGCCTGA[G/T]GTCCAGGGTTGACTT	220441
rs572891511	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61826179	GGCATTTGAGACTCA[A/G]TAGATGCAGAAAGAA	220441
rs572900302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61871807	TTTAGTCTCAGGTTT[C/T]ACAACTATAAAATAA	220441
rs572911068	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808662	TGAGTGAGGCAAACA[C/T]AAACAAGTGGTGAAA	220441
rs572930950	snp	A/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61847212	ACAAAAAAAGAGGTA[A/T]CAGAGTAACATTTAA	220441
rs572946830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864847	AACATGGTGAAACCC[C/T]GTTTCTACTAAAAAT	220441
rs572949366	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61872968	TAGCTTCCTTTGGTT[C/G]GTACTTTTCAATAAC	220441
rs572959227	snp	C/T	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61839578	TGTCCCTCCTTGGAT[C/T]CTCCTCCTCTTTTTA	220441
rs573008953	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840298	AGTCTATGGTATTTT[G/T]CTATAGCAGCCTGAA	220441
rs573134492	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834210	GCCGTTCTTTCTCTT[A/G]TCTCATCTCTTGGGA	220441
rs573170304	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61874221	CCTAATATTACCTCC[A/T]CGCTGCCGCAGTTTA	220441
rs573246034	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880395	AGTGTGGCTCACAGG[C/T]AGTTAAGAGGAAGGA	220441
rs573262415	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61877108	ACAAAGCTTCCAGCC[A/G]TCGAAAGACTCATCC	220441
rs573275239	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61852006	TATGAGGCAAATGAC[A/G]TCACCTACTGTCAAA	220441
rs573275589	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809828	TAGGTGAGATATATA[C/T]AGTGGGATACCCCAG	220441
rs573278446	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61891787	TTAACTTCATTTTTC[A/G]AGGGATTTGGAGGAA	220441
rs573365383	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61853600	CTCACCGGTTCCTTA[A/C]CTTTTTTAGCTGCCA	220441
rs573387981	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF152	GRCh38.p7	18:61807894	TGTTCTTTGGCCTCT[C/T]GGAGGAGCTACTTGA	220441
rs573398651	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61842958	TGAGATTTGGGTGGG[A/G]ACACAGAGCCAAACC	220441
rs573466526	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814751	ATTTATTAAAATGCC[C/T]GCCTGGGTTGACCAT	220441
rs573496196	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864683	GGTTCCTCTGGCGAC[A/C/G]AGCTGGCACTCTGAG	220441
rs573508445	snp	A/C	0.00159617	0.0282053	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815204	TCCATAAACACGTAG[A/C]AAGCTCTAATTACAA	220441
rs573518796	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827154	TCCTTATAGTCTGAA[C/T]TTTGGCCATAATTCC	220441
rs573544140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819965	GGCGGAGATTGCAGT[A/G]AGGCAACATCGCACC	220441
rs573580695	snp	C/T	0.00358779	0.0422022	downstream-variant-500B	RNF152	GRCh38.p7	18:61807755	TGCAACAAGTTGTTC[C/T]GTATATGGTTCACTT	220441
rs573594113	snp	A/C	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61884295	ACGTGAAATTTAAAC[A/C]CAAACCCATCTTACT	220441
rs573617432	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811960	AAATCTATAAGCAAC[A/C]GTTCCAAAGGGCAAC	220441
rs573626378	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61814122	TCATGCCAATTAGCA[A/G]TATTAGCTTTGTATT	220441
rs573663279	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61876500	TCTTTTTAAGCATCA[C/T]ATACAGATGTTAGTC	220441
rs573688410	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814702	CTGGCTTAACTCTTG[A/T]GGAAGAGCATCTTTC	220441
rs573744314	snp	G/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61878369	TCAAAATGCTGAGAT[G/T]CTGGTGAGCATCTAG	220441
rs573746859	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896375	GAGACTTCAGGAGTG[C/T]CACCATGCCCAGTTA	220441
rs573777726	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61852561	ATCTAGATTGTCAGT[A/C]TTCAAAGAGAAACTG	220441
rs573787588	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844947	CTAACAAAGAGCCTA[C/T]TTCATTCATTTTATT	220441
rs573810902	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61891164	ATTGTAGAAAGGAAG[A/C]AGGCATTGGAGGCAG	220441
rs573814600	snp	G/T	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61845926	GGCTTTGTGTGGGGG[G/T]GCGTGGTGATGAGGA	220441
rs573841107	snp	A/C	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61871776	TGCAGAGCCCTTGGT[A/C]TATCAAGTTACCTCT	220441
rs573845653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840246	TCCCAGCCCCCAGAA[C/T]TGTGAGAAATAAGTT	220441
rs573881125	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61885053	GACACCTCTTTACCT[A/G]CATGGTTGAATTAAC	220441
rs573882674	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833790	TTGAAGAGATTTTTC[C/T]TTCTGTCCATAGATC	220441
rs573907295	in-del	-/C	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61820152	GCTAATATGGTGAAA[-/C]CCCCGTCTCTACTAA	220441
rs573907768	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61840873	TTTTGCATTTCAGAG[C/G]CTTTTCCCCTTCCCT	220441
rs574051549	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882528	AACTGGCAACCAACA[A/G]ACTAATCACTGTTGC	220441
rs574066584	in-del	-/AG/G			intron-variant	RNF152	GRCh38.p7	18:61844101	AAAGAAAGAAAGAAA[-/AG/G]GAAAGAAAGAAAGAA	220441
rs574072692	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61837934	ACAAAATCCAGGCCT[C/T]ATCTCCTGCCCTCCT	220441
rs574082207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61838630	ATAGATAGCCACAGA[C/T]GGTCCCCAGACAGCA	220441
rs574087382	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829048	GAGACCAAGACGAGG[A/G]GAGGCAGTGCCCAGG	220441
rs574099699	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61832500	ATAGCTACGCATACC[A/C]TGTAGAATTAAGCCT	220441
rs574126295	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864792	GTGCTCACGCCTGCC[A/G]AGGCAGGTGGATCAC	220441
rs574163086	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61858739	TGGCCATCCCCATCA[A/T]CACCCCTGGCTATTT	220441
rs574261321	in-del	-/CAGAAAAGACT	0.0111196	0.0737302	intron-variant	RNF152	GRCh38.p7	18:61860038	TAGTGTCCTTTAATA[-/CAGAAAAGACT]CAGAAAAGACTCACA	220441
rs574321160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819158	GTCTTCTCTAAGAGT[C/T]TGATCGTTTTAGCCC	220441
rs574342055	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825546	AGCATCATACAGGGA[A/G]ACTCCAACCACAAAC	220441
rs574406843	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61834909	TCCACTGAAAACCTG[A/T]TAAATCAGCGTCTGG	220441
rs574418352	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61830225	GATGGGGGTGTCTTG[C/G]TATTTGGCCAGGCTG	220441
rs574476239	snp	A/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61821898	TTTCATCCTGAAACC[A/T]TCGGTCCCTACCCAT	220441
rs574479279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61879952	CCAGGGCAACAAGAG[C/T]GAAACTCCATCTCAA	220441
rs574548969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862375	CTGCCCAGAGAGGAG[A/G]TGACCATCCTGAAAA	220441
rs574579682	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812761	AACCACATGGTTTGA[C/T]AGTTGTCTTTCAACA	220441
rs574600661	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829813	ATGAAGAATGGAAGA[A/G]AAAGACCAGTCCCCT	220441
rs574627224	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861798	GTGAGGAGGCAGGCT[C/G]TTTGTAACAACCAGC	220441
rs574633999	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853208	TCTGGAGCCCAGATG[C/T]CTGAATTGGTCTCCT	220441
rs574637147	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61882876	CCCCCTCCACCCAAC[A/C]CACACTACCATCATG	220441
rs574704022	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61845569	AGGTTTGGAAAGTTT[A/T]TATAACGTTTCATTT	220441
rs574706203	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813849	TCAGACATGCATTAT[A/G]GCAGCCTGGGAGAGT	220441
rs574713544	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61848689	ACCTCAGGGTGGAGG[A/G]GGCAAGACAGCAGCT	220441
rs574752736	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854140	AATATTTTTTTCTTT[A/T]CCAAGCTTCCACTAT	220441
rs574790501	snp	A/G	1.86705e-05	0.0030553	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816508	AAGGTGAAGGGGAAG[A/G]AGCTGCTTCTCAGAG	220441
rs574849137	in-del	-/CAC			cds-indel	RNF152	GRCh38.p7	18:61813305	ACACACACACACACA[-/CAC]ACACACACATACACA	220441
rs574860933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866801	CTACTTGCCCGCTGT[C/T]CCCACCGCTGAGCAG	220441
rs574877784	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814535	ATCTATAGATCATTA[A/C]ACATTTAAGAACATT	220441
rs574919497	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873052	TGCTTCTACGTACCA[C/G]ATTTGGGGTTCTGTC	220441
rs574971082	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61866323	GGGGACTCGTTTATC[C/T]TCAGGACAACTTGAG	220441
rs575004228	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808941	TCCTTGGACCCTCAT[A/G]AGCTGAGCACATTAC	220441
rs575018940	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886989	AGGCTTCGATGATAG[A/G]ATAGAGGCAGAGGAA	220441
rs575084461	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61809380	CCTTTAAGAGGCATT[G/T]GTCATCTCTATTTCC	220441
rs575092659	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886246	ACTTCAAGCTAAAAG[A/G]GTCTAAAATTCCTTT	220441
rs575113664	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61874420	ACGTTTCTTGATGAA[A/G]GAGCCCTCAATCAAC	220441
rs575184346	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873549	CATGTTGGTCAGGCT[A/G]GTCTTGAACTCCTGA	220441
rs575186140	in-del	-/GCATCAG			intron-variant	RNF152	GRCh38.p7	18:61880735	TAATAACTTCAATTT[-/GCATCAG]GCAAAATGTTTTTAA	220441
rs575218901	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61852713	GATTCAATTGTCTTG[C/G]GGGTGCTGCCTGGAC	220441
rs575229454	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893211	AAATCGGAGCAGGTG[G/T]GGAATAACATCTTGG	220441
rs575238211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61841039	TACTGCAGGAGGCTG[A/G]CATGGGGTGAGAAAG	220441
rs575273719	snp	C/T	0.00597247	0.0543191	intron-variant	RNF152	GRCh38.p7	18:61859437	CAAGGCTAAGGGTTC[C/T]GGAGAGTCAGGGAGC	220441
rs575285178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61833703	AGGGACTATGCATTT[C/T]AAAAATGTCATCCAT	220441
rs575372137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61827049	TATTTCAACAATATG[A/G]GCAATGGCACCAAAA	220441
rs575462500	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61866961	CCCTTATAAGCTGGG[A/G]TGGAGGGATGGGAAG	220441
rs575502440	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61865603	AATCCAAGTACTAGA[A/T]AATCCCCTGCTAGCA	220441
rs575509010	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61860118	GAATGCCAAGGACTG[A/C]CGACAGCACGAGAAG	220441
rs575525235	in-del	-/GT			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812277	AAGTCAATGTGCCTG[-/GT]GGCTACCGTACCAGA	220441
rs575535276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61820506	ATCAGGTGAGACTAT[A/G]ATTGACTCTACTGAG	220441
rs575535410	snp	A/C	0.00993419	0.0697739	intron-variant	RNF152	GRCh38.p7	18:61820142	AGACCATCCTGGCTA[A/C]TATGGTGAAACCCCG	220441
rs575561427	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61828575	GACTACAGGTGTACA[C/T]CATTGCACTGGCAAA	220441
rs575563193	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835446	TATATTTGTTTATTT[C/T]TACAAAAATAAACCC	220441
rs575617487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61824577	TCTAGCTAGAGCCCA[C/T]ATCCTAACAGAAAAT	220441
rs575634199	snp	A/G	0.00159617	0.0282053	intron-variant	RNF152	GRCh38.p7	18:61866252	CTGCTTCTAGACAGC[A/G]AGTCGGGCCCAGGTA	220441
rs575725511	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892613	TCCAATGGCTTCTTC[A/G]AAGGGAAGGTATAAA	220441
rs575818022	snp	A/G	0.0130921	0.0798413	intron-variant	RNF152	GRCh38.p7	18:61829311	ATGACTAATCAGCCC[A/G]GCCAGAGGAGGCACA	220441
rs575822382	snp	C/G	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814884	ACAGAAGAGGAGCGA[C/G]TGTTGCAGGTGACGT	220441
rs575902251	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61842980	AGCCAAACCATATCA[C/T]CCTGTTTCATGACTG	220441
rs575905941	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815358	AAAAGCCTTAGCAAC[G/T]AAATGAAGACTGGGT	220441
rs575944581	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61863153	TGAAAAGTAGTCCCT[C/T]AGCCAGGCGCGGTGG	220441
rs575981319	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61883145	CCACAGTGTTCAGCC[A/C]CTCAACCTGTCCTGG	220441
rs575994904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61863398	GGCGATCGTGCCACC[A/G]CACTCCAGCCTGGCA	220441
rs576026030	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810760	CTACTGAATTATCTC[A/C/G]ACTATCTTATTATTC	220441
rs576058259	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61869579	TTACACTCACACCTT[C/T]AATAAAGGATGTAGC	220441
rs576066652	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61863403	TCGTGCCACCGCACT[C/G]CAGCCTGGCAACAGA	220441
rs576155620	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61818707	AGGATATAAATCAGA[A/C]CCAGATTCTACCCGA	220441
rs576188457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61844413	TATGAGTAACAGACT[A/G]TTGGAAAATCATAAA	220441
rs576225219	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888058	TTTGAGTAAGTTTCA[C/T]CATGCAGGATGTTTG	220441
rs576259489	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811679	CTTATATTTGCACCT[C/T]ACTAATACAGCAATG	220441
rs576310827	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867630	GAAACTGTTATGGCA[A/G]CCCCCAACCCAGGGT	220441
rs576363482	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895308	CCTGCGGACGTTACC[C/T]GGTCCCCAGCAGCAG	220441
rs576435398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61862329	TTCCCATTTCACACA[C/T]GAGGAAACTAAGGCT	220441
rs576473680	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61848941	ACAGGGATGCAGAAT[C/T]TCCAGCACAAACCAA	220441
rs576491899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836232	CTTTTGTGCCATCAC[A/G]TGGGGACATGGGGAC	220441
rs576510124	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61849517	GATTGAAGTAACCTG[A/C]CCAAAGTGGCCACTG	220441
rs576578526	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61836896	GCATAAATCATCAAT[A/G]GATGCTAAAATCATT	220441
rs576594383	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815158	TTTCTCATGATTTCT[C/T]GGTTTATTGCTCCCC	220441
rs576594702	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61856918	TAGTGTCACCTAAGC[A/G]TTATTTACAAGCATC	220441
rs576613286	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61886063	ACAGGCTTTGAGTAA[C/T]AACTAATTTTGTTAG	220441
rs576628947	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61816758	TCCCATAACGCCCAG[C/T]GAAAGGCGAATGAAA	220441
rs576630945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61857335	CTGGAAACCACACAC[C/T]ATGTCCACATGATTT	220441
rs576656360	snp	C/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892676	TTTTAGCAGCCCCCA[C/G]ACCTTCTCACAGATA	220441
rs576666561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842944	TGGGAGCTACAAGAT[A/G]AGATTTGGGTGGGGA	220441
rs576673962	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61881286	AGCTGTTAAGTACTA[C/T]AGATTATAGCGAACG	220441
rs576694293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61843550	AACATGGGAAAATAC[C/T]CAAATGCCCACAGAC	220441
rs576703201	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61836339	TGCTATAGGCCGAAT[A/G]TCTGTGTCCCCCCAA	220441
rs576725978	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61868350	CAGGACAGAGGTAAA[A/C]CCAGCCCAGCCACCC	220441
rs576734038	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858202	CACTGACTGTGGGCT[C/T]GGCTGTGACCTCCTG	220441
rs576760089	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61874943	AATAAGTAAGATGCT[G/T]GAGATGCAAAGATGA	220441
rs576808786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61880742	TTCAATTTGCATCAG[A/G]CAAAATGTTTTTAAT	220441
rs576818916	snp	C/T	1.67713e-05	0.00289575	synonymous-codon	RNF152	GRCh38.p7	18:61816398	CAACTTGGGCCTGCG[C/T]CGGGGGCTGTAGTAA	220441
rs576855759	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810132	CACTCCCAAAGGTAG[C/T]TAGTTTGACATAATG	220441
rs576858566	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61885700	ACACTCTCATAATGA[G/T]CAAGCATTTTGAGTA	220441
rs576920348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61829896	TCAGGGGGGCAAGTG[C/T]AACCATTATAATGGC	220441
rs576925776	snp	C/T	0.000399281	0.0141238	synonymous-codon	RNF152	GRCh38.p7	18:61816119	GCGGCAGCCCATGTC[C/T]CCGGGCAGCAGCGCA	220441
rs576936020	snp	A/G	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61822912	AATCTTCAACAAAAT[A/G]TAAATATTTGAAATG	220441
rs576970832	snp	A/G	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61850563	AAATTTCAAGTTACT[A/G]AGAGGCAGACTCAAG	220441
rs577027964	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61823925	GGACTCTGCTAGGGC[A/T]TGTGCCAATTCTGTC	220441
rs577047987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61835642	AAATCAAACCCTAAA[A/G]TTAAATACAAACAGA	220441
rs577051717	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860467	ATTGCCTGGTGATAC[A/G]GCCATCAGAGCATTG	220441
rs577100058	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF152	GRCh38.p7	18:61811622	GCTGGCCAACTTCAA[G/T]GGCAAACAAAACCAG	220441
rs577130885	snp	G/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61854951	GATAACTCACAGACT[G/T]TCTCAAATGCTACAA	220441
rs577153195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61842274	TTAATTCCACATTAT[A/G]AACATTTCCTGAAAG	220441
rs577171917	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61817177	AAGAAGCACACGAAG[C/G]CATCTTTCATCTTTC	220441
rs577172294	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848322	AAGATATCAGTGCTT[C/G]CACAATTTTTCTAAC	220441
rs577176507	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61863062	AAAAAAATTTTGAAG[-/A]CAGGTTAACCAAAGG	220441
rs577213572	snp	C/T	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61817826	GAAGTTTGGGAATGT[C/T]CTCTAACGCTCCACT	220441
rs577279884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61861642	TTTATAAAGAAAACA[A/G]GTTTATGTAGCTCAC	220441
rs577305399	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827726	ACGAGTTAAGCCTTA[C/T]ACTGAAGTTGCAAAG	220441
rs577329276	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867215	TAATCCCAACACTTC[A/G]GGAGGCAGGTGGATC	220441
rs577343700	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61824901	ACTGTCAGGAGATCC[A/C]CAGGCTCCCTGGAAA	220441
rs577395535	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61873765	TGAACATCAGTTTAC[C/G]TGACATATTTTCTGA	220441
rs577464105	snp	A/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61848751	GGAAGAGGCCTGCCC[A/G]GCAGGAGCTGATGTA	220441
rs577487503	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895110	ACCTAACTTCGACCT[A/C]GGGAGGTGCTTAGAA	220441
rs577563440	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879868	TACTCAGGAGGCTGA[A/G]GCAGGAGAATCGCTT	220441
rs577626185	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61861439	CTGTATAGCCTATAT[G/T]TGTACTGGGCTACAC	220441
rs577628417	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61819064	AAAGGAAAGAAGGTA[A/C]GCGATTACAGAATTA	220441
rs577645072	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF152	GRCh38.p7	18:61833316	CTAACTAATACTCTC[-/A]AGTTATTGAGTAACT	220441
rs577661400	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61882475	GGCACGCAAGTGTCT[C/G]GCAATTGCCTTCAGG	220441
rs577717550	snp	C/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61852458	CCACAATTACAGCAT[C/T]GCTCATACACTGATC	220441
rs577848083	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61845882	ATATGTTGAAACCTA[A/T]TCACCAATGTGAAGG	220441
rs577893321	snp	A/C	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61891629	TGGCCTTTGTTTCAC[A/C]TGGGACTAGATAACT	220441
rs577898540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61877167	CTCGGCTGTTGTCAT[C/T]CACATGGGCACCAAA	220441
rs577924849	snp	C/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61876348	ATAAAAATAACCAAA[C/T]CAACATGCTAATGAA	220441
rs577932909	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61851091	TATCCACAATGATTA[-/A]AAAAAAAAAAAAAAA	220441
rs578076164	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61870095	CCAAACCTCACGCTC[A/T]CTTGGAAAGAAATAA	220441
rs578091647	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61825406	GAAAGGACATTTGGA[A/T]TTTAAGGAGCCTACA	220441
rs578140424	snp	A/T	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61864280	GGCTATCAGTGGGGT[A/T]TCTCACAACCCCCTC	220441
rs578207054	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61844763	CCTCTAATGAGGGCA[C/G]TAAGATGCAATGAAA	220441
rs578237557	snp	C/G	0.000399281	0.0141238	intron-variant	RNF152	GRCh38.p7	18:61831552	CAGGAACTGAAATGT[C/G]AGGTTATGGATTATT	220441
rs578240062	snp	A/G	0.00279162	0.0372561	intron-variant	RNF152	GRCh38.p7	18:61838529	TGGACCTCAGTGTGA[A/G]CTTAAACCAACCCCC	220441
rs578243123	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61864532	CCTGTCACTTAGGGG[A/T]TTGATGGAGGCTTCG	220441
rs578262363	snp	A/T	0.000798403	0.0199641	intron-variant	RNF152	GRCh38.p7	18:61832325	TTAAGCGCACATGTA[A/T]ATATGTACTACTTAA	220441
rs745323551	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61847580	ATGGTGTAAACATTT[A/C]TTTTTCTTAAAACAC	220441
rs745341751	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836351	AATGTCTGTGTCCCC[C/T]CAAAATTCGTATGTT	220441
rs745374412	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811247	AATAAAGGGATGGGA[A/G]CTCTTAAAATCAAAA	220441
rs745375648	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812277	AAGTCAATGTGCCTG[C/G]TGGCTACCGTACCAG	220441
rs745416550	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61885420	TCAGGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG	220441
rs745521603	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858631	CCCACCAAGCCAGTC[C/T]GCAGTACTCATTCCT	220441
rs745550359	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61883968	AACTCCCATGTAAAC[A/G]CTGAAGGCTGTAGTT	220441
rs745601848	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61817212	CAAATCATTTGAAGA[A/G]AACAAAACAAAAAAC	220441
rs745620959	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828492	TGCAGTGACACAATC[A/G]TAGCTCACTGCAGCC	220441
rs745635597	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854314	ACAATGTCACAACCA[C/T]CTAAGAGACTGGTCA	220441
rs745685883	in-del	-/TCACAC			cds-indel	RNF152	GRCh38.p7	18:61813278	CTCTCTCTCTCTCTC[-/TCACAC]ACACACACACACACA	220441
rs745713660	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61891093	AGTCCATTATCTATC[A/T]CAGAGTCCATTATCT	220441
rs745733581	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879554	GGATAGGGAGAAAGC[A/G]TGTTCCGGGGAAAGG	220441
rs745790120	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863659	GCAATCCTGTGTAAC[C/T]GTATGGCCTGTCCTC	220441
rs745835528	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864394	TGGTTTATGATAACA[A/G]ATACAACTCAGATCA	220441
rs745875183	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61834226	TCTCATCTCTTGGGA[G/T]GCTGTCCTTTTGGTC	220441
rs745980347	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823955	CGCTACAAAACTCAA[C/T]TAACCAAGCACCATG	220441
rs745984889	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836137	AGTAGCATTTCTCAC[C/T]AAAAAGAAGCTGACA	220441
rs746010298	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61880609	TACAGTTATCTCCCC[C/G]ACTCTCCCAAATTGT	220441
rs746057472	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61854919	AGCAGCAAGTTACAT[C/G]ATTTTCCTGAACTAC	220441
rs746100430	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869948	GTGTCACTAGGATTT[A/G]CTAGAAGCATTTGTA	220441
rs746143818	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61844436	ATCATAAAAACAATA[C/T]CTTACCACTATGCTT	220441
rs746148460	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61820344	ACCAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA	220441
rs746320087	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61887537	GCCTGGCCAACATGA[G/T]GAAACCCTGTCTCTA	220441
rs746392554	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888225	TAGGCCAAGAAATCA[C/T]GGACATCAAGAACCA	220441
rs746399419	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61875912	ATATTGATGACTGCC[A/C]GATTAAGCTTCTAAA	220441
rs746492202	in-del	-/AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA			intron-variant	RNF152	GRCh38.p7	18:61844090	AGGAAAGAAAGAAAG[lengthTooLong]AAAGAAAGAAAGAAA	220441
rs746495244	in-del	-/CCCA			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61839041	TAATGTTCATCAGAT[-/CCCA]CTCTGTGGCCAAAAA	220441
rs746525804	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61828785	ATTGAGTATAAGGCA[A/C]TACTCTAGGTTTGGG	220441
rs746537615	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61875714	TGAATACCTGTGTAT[A/G]TCTCACCACTCATTC	220441
rs746565792	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61864634	AGGAGGTCTGGGATG[A/T]GGCTGAAAGTCACAA	220441
rs746602204	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885782	GAGGTAAAACAGATG[C/T]ATATCACAAAGGTAT	220441
rs746647118	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61859573	TGTGTCTCCCAAAAA[C/G]ATAGTTTGAAATCCT	220441
rs746723281	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811046	AGATTAGTATCTTGG[-/A]CAAAAAAAAAAAAAT	220441
rs746813307	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808752	CCCAACAGTACTGAC[A/C]TACTCAAGTCAGGAT	220441
rs746832669	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861570	TGACTGTACATGTTA[C/T]GCTTAGTGTCTTAGT	220441
rs746860620	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891463	ACACCCTTGTTTCTA[C/T]TGCATTATTACATTC	220441
rs746886550	in-del	-/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894794	CGCGGTGGGTGGGTT[-/G]GGGGGGTGCCCAGTC	220441
rs746933773	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61865304	CCCTACTGAAAAAAT[A/G]TAAGGTTTCTTCTTC	220441
rs746937891	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61854506	GGAAACCATCCTCTC[A/C]ATGATTTTCCATAGT	220441
rs746952264	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61855261	TGTAAGAGAATTCTG[C/G]TTTACCAGGAGTCAA	220441
rs746971714	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880779	GCCAACACCACCATA[C/T]AAACAACAGTTGTTC	220441
rs746995328	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61892201	TCTAAATGGAAACTT[C/T]ACTCAAGCTGTTTTC	220441
rs747009578	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829765	GGAGTAGCTGGAAGC[A/G]GAAGTTCTTATGTTG	220441
rs747068733	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61861799	TGAGGAGGCAGGCTC[G/T]TTGTAACAACCAGCC	220441
rs747134555	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61876026	ACCAACCTTTCCAAT[-/C]CTTTTTCATACTATT	220441
rs747152928	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61821916	GGTCCCTACCCATCC[A/G]TCCTGTGGAAAAATT	220441
rs747154692	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61820047	AAAAAAAAAAGAATC[A/C]GGCCGGGCATGGTGG	220441
rs747167288	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61845400	CACACATCAGCCCCA[A/G]CCAGCTGGGCACGCA	220441
rs747212311	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61860874	CCCTAGGCTAATGTG[A/T]GTATTTGTGTTTTAG	220441
rs747251707	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61872205	ATCAGGAGAACAGCA[C/G]CAAAAGGATAGTGCT	220441
rs747303037	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61824235	TATTCTGTCGTTACA[C/T]AGATAGGTTACCTTA	220441
rs747315410	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841806	TCACTAATCCTGCTT[C/T]CAGTGGCAAGGCTGT	220441
rs747377819	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867904	AAAAATACACAAAAC[A/G]CACATAAAAATACAA	220441
rs747398332	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896073	TGACTGATCCTTATC[C/T]CTTTGTTCACCCAAG	220441
rs747415470	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831710	CAAACAAAAACCACT[A/G]TAAATACAATTTCTA	220441
rs747475848	in-del	-/TG			intron-variant	RNF152	GRCh38.p7	18:61865655	TTAGTTTAGAGTCTC[-/TG]TTGCCACAGAGAGTT	220441
rs747485242	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877200	AAACCATTTGACTTA[C/T]GTATTTTGGTCAGGG	220441
rs747496328	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877848	CATCCCAAATGTCAG[A/G]GAAAGTCAGACAGTA	220441
rs747541958	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866703	GTGACATGTTCATCC[C/T]TTCATCAACCATTCA	220441
rs747570247	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866547	CCCAGCAGGGCCTAC[A/G]CATCCTTTGGTGACT	220441
rs747581813	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61841103	GAAGCTGATCAGAAG[G/T]CAGGCTCGGTCCATT	220441
rs747591039	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61830138	GGGATTCTCCTGCCT[C/G]AGACTCCCGGGTAGC	220441
rs747600963	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61850697	GACAACAAAGTAAAC[C/G]TGTATGTGAATGCTA	220441
rs747612681	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61855345	GATGATATCATAGTG[A/T]TGGCAGAAGCGGCCT	220441
rs747672224	snp	C/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892605	CACCTACCTCCAATG[C/G]CTTCTTCAAAGGGAA	220441
rs747673091	in-del	-/AAAC			intron-variant	RNF152	GRCh38.p7	18:61846265	TTCTTTTTTAATAAA[-/AAAC]AATCCCAAAAAACTG	220441
rs747791328	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831656	AATGCTCACTTCCTA[A/C]TGTCACTAGCTACCC	220441
rs747817714	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61850199	AAGTTATCTAACCTT[G/T]TTATTCTTCAATGCC	220441
rs747869820	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61887806	AGTGAGGAGTGCACC[A/T]AGTGTGATTATCTGG	220441
rs747877531	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61846684	AACACCTGGCACCAG[A/C]AAGGTATTCTGTACA	220441
rs747961513	snp	G/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809783	TAAAATCGAGCTAAT[G/T]AGATGAGTATTTCAA	220441
rs747972738	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61881896	TCTTCTTATAGGACA[A/G]TGTGGACTGCCTTGA	220441
rs747993623	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872377	AGTTCCTTCCAGTCC[C/T]AGAGGTGGAAACTTC	220441
rs748000323	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825383	ACTATCATTGCCTGT[C/T]AGAGCCAGAAAGGAC	220441
rs748000508	snp	A/G	1.65138e-05	0.00287343	synonymous-codon	RNF152	GRCh38.p7	18:61816107	CCCGGGCAGCAGGCG[A/G]CAGCCCATGTCTCCG	220441
rs748042834	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61841721	TGCAATCACTTAAGC[A/C]TCTCCATGAAACCGC	220441
rs748074790	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808831	GTCTGTCTGCACTGA[C/T]GTGGCAACCAACTCT	220441
rs748126048	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61841235	CATTAAAAGTCACTA[A/C]AAAGGCCTAAAATTC	220441
rs748128984	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61863434	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	220441
rs748199551	snp	C/T	1.65021e-05	0.00287241	synonymous-codon	RNF152	GRCh38.p7	18:61816323	GGGGCACCGCACATC[C/T]TTCTGGCTGGTCCTC	220441
rs748278785	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890127	TTGGAATAGTAAATA[C/T]ACAGGTTGTAAATTA	220441
rs748290322	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817068	AGATTTAGGCAACTT[C/T]ACAAACCTAGGTACT	220441
rs748322190	snp	C/T			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61852154	TCTGGAAACAGTGGT[C/T]CCAAAGGAAAACATT	220441
rs748403661	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889216	GATACTGATATCCCC[C/T]CAGTCACTGTGACTT	220441
rs748458530	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61821930	CGTCCTGTGGAAAAA[C/T]TGTCTTCCACAAAAC	220441
rs748472423	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61834393	CCACTTCTATGTTCT[-/C]CTAGGAACCTTTCTA	220441
rs748493777	snp	G/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811525	AAACAATGTCAAATC[G/T]CATTCTAAAAATACT	220441
rs748546356	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823045	AGAATGGGAATGCCC[A/G]GTGACAGATGTGTCA	220441
rs748587082	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61834023	CATTCACTCAATCAA[C/T]CATCCAATGCTTTAT	220441
rs748646655	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879157	AAAATATTCAGGAAA[A/G]ATAATACTAAATGGT	220441
rs748667886	snp	C/T			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892670	CAGGAGTTTTAGCAG[C/T]CCCCACACCTTCTCA	220441
rs748670379	in-del	-/AAA			intron-variant	RNF152	GRCh38.p7	18:61884445	TAGCTTTGCCATTAC[-/AAA]AAAAAAAAAAAGCAG	220441
rs748681081	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61867965	AAATATGCTAGCTAA[C/T]ACAAACAATATATTA	220441
rs748704644	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61844379	TTATAAAATCTCACA[C/G]AACAAACCTGAGAGG	220441
rs748741158	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831669	TACTGTCACTAGCTA[A/C]CCTCAAAGCAGAACA	220441
rs748807750	in-del	-/AGGAGGGAGACGGGAGGGGAGGGGAGGGC			intron-variant	RNF152	GRCh38.p7	18:61844221	GGAAGGAGGGAGGGA[lengthTooLong]AGGCCCCATAGTATC	220441
rs748828483	snp	A/G	1.64958e-05	0.00287187	synonymous-codon	RNF152	GRCh38.p7	18:61816179	GTAGCACCCATTGCT[A/G]GGAAGTTTGATGAAG	220441
rs748868206	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61830224	AGATGGGGGTGTCTT[G/T]GTATTTGGCCAGGCT	220441
rs748925333	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815332	GTTTTGGTGCCATTC[-/A]AAAATGTATTAAAAG	220441
rs748930397	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811302	TATCAGTAAGAATCT[C/G]GTCTTTATAGGAAAT	220441
rs748946098	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866566	CCTTTGGTGACTTGG[C/T]TACATTTCCAGCCTC	220441
rs748948989	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61847858	TCAAATGCTGATGTA[-/T]TTTTTCCTTTTCACC	220441
rs749015615	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61819128	TTGTTTCTAATACTA[A/G]AGCAACTTACAGAAG	220441
rs749034521	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61830910	GAATCTTGAGATTTT[A/G]TACCTAGCAAAGTCC	220441
rs749100757	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841857	CTTTGCACAGGGACA[A/G]ATGGTAATATTTTAG	220441
rs749133054	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61822528	GGTGGTAAAATAGCA[A/G]AGATCTCCAACATTG	220441
rs749161389	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846766	ATTAATACTGCTCTC[C/T]TCACCTTCATTAGTA	220441
rs749168021	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61889593	GTTGCTGATGGAAGC[A/C]CAAATGTCCCTAAAC	220441
rs749194943	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61862245	CACTAGATGCAGTAC[C/T]TTCATGTCTACCACC	220441
rs749275034	snp	A/C	1.65179e-05	0.00287379	synonymous-codon	RNF152	GRCh38.p7	18:61816098	CTGCTGGCTCCCGGG[A/C]AGCAGGCGGCAGCCC	220441
rs749279131	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61836189	CCAGGTCTGGGGCAG[A/G]GAAAATACAAAGTGA	220441
rs749283146	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832316	GTTTTTGTTTTAAGC[A/G]CACATGTATATATGT	220441
rs749284087	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811163	ATGAAGTAAATGTAT[C/T]TTGTATATATTCCAT	220441
rs749404589	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61890265	GAAGTCACTAGTGCT[A/G]CTCACCCATATCCAC	220441
rs749409660	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869117	AAAATTTCCTAAGTT[C/T]ACCATGTCTCTCTAA	220441
rs749440180	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844097	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs749458525	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61834353	TCCAAGAAGCTTTCC[C/T]GTTCCCCTCCAGCTG	220441
rs749496427	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879436	CTTGGTTTCTAAGGG[A/G]GTTCCTGGAATCAGT	220441
rs749508748	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817172	TGCAGAAGAAGCACA[C/T]GAAGGCATCTTTCAT	220441
rs749511314	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853201	TTATAGGTCTGGAGC[C/T]CAGATGTCTGAATTG	220441
rs749529705	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61842003	TACAAAAACATGAGG[G/T]GGGTTGCATTTGACC	220441
rs749595881	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812655	AAATTCATGCTTCTT[A/G]TAGTTTACTATTTAT	220441
rs749683719	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813403	CAATGTTTCTTAGGT[A/C]AGTAAGACTCACAAA	220441
rs749688736	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873626	GGCATGAGCCACCAC[A/G]CCCAGCCTCAGTCTC	220441
rs749722831	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887049	GCTAGAATAAGAAAG[A/G]GGCAATGAAAAACAT	220441
rs749777773	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859083	ACCCTGTATTATAGA[C/T]GAGGGCTGGTGGCTC	220441
rs749798221	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859782	TACTTAGGAGGCTGA[A/G]GCAGAAGAATGGCTT	220441
rs749820527	snp	A/G	4.94694e-05	0.00497316	synonymous-codon	RNF152	GRCh38.p7	18:61815885	AGTGAAGCGCTTAGA[A/G]ATGCAAGACATGTTG	220441
rs749845759	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885838	TGGGGCAGTCAGCGG[C/T]GGGCAACTACACCCA	220441
rs749870357	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823186	TTTGACAAACCTCAA[C/T]TGAGAATTCCATTGG	220441
rs749888037	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61822833	CAGAGATTAAACTAG[C/G]CACTACATTGCTTTT	220441
rs749900888	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859438	AAGGCTAAGGGTTCC[A/G]GAGAGTCAGGGAGCT	220441
rs749924433	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61833754	AAGCAGATAAAGAGA[C/T]AAAAGCATTCTGACA	220441
rs750022262	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871609	AGAAATGACTCTCTA[A/G]TGGTAAAACCAGGCT	220441
rs750045224	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869483	CACCTCACCACAGAC[A/G]GCACTAAAGGTGAAC	220441
rs750079242	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61868794	GAAAAGCATAAATCA[G/T]TAGTGTGCCTTGTAG	220441
rs750106219	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61844195	AGGAAGGAAGGAAGG[-/G]AAGGAGGGAGGGAAG	220441
rs750118674	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61832986	CTTAATTCAAGATGT[C/T]TGTCAAAGCAGAAGA	220441
rs750182127	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61865027	CTCCATCTCAAAAAA[A/G]AAAGGAGTTTATGAT	220441
rs750184105	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876285	TTGCATCCCTTTGTA[C/T]GCATGTTCTTACTCC	220441
rs750209168	in-del	-/GAAAG			intron-variant	RNF152	GRCh38.p7	18:61844094	AAAGAAAGAAAGAAA[-/GAAAG]AAAGAAAGAAAGAAA	220441
rs750218504	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61829610	AAGGAGAGAGAGAGA[C/G]AGAGACATCCTAGGG	220441
rs750252708	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61840272	AAGTTTCTGTTGTTT[A/C]TAAGCCACCCAGTCT	220441
rs750337324	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888005	TGCTCAGCCCCTCCT[C/T]TGCATGAAAGGCAGG	220441
rs750350607	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860370	AGAAAATGCAGTCAC[A/G]CACCACATAACGTTT	220441
rs750367350	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61886753	CAAACAAGCTTGAGT[G/T]AATTTCTATTCTTTG	220441
rs750376567	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875575	GGCGTGGATTACCCA[C/T]GAAGGTCAGCTCTGA	220441
rs750407289	in-del	-/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811047	AGATTAGTATCTTGG[-/C]AAAAAAAAAAAAATT	220441
rs750442636	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61849858	AGGTTTGAGCCACCA[C/T]GCCCTGACATCATCA	220441
rs750457629	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61885614	CGCCCAGCCGAGAGC[A/G]TTATTTTAATATTAA	220441
rs750461106	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61845104	TTTTGTTTGTTTTCA[C/T]AGACAGGATCTCACT	220441
rs750499963	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846381	TCATCTCCCTCTACC[C/T]ACTGTGCCTATGCAA	220441
rs750500866	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61819575	GCAATGAGGTTGTAC[A/G]GTGAAAGAAGCCAAA	220441
rs750552989	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61835084	ACACTGCTAAATGGG[A/C]GAAGAAAATGGTAGC	220441
rs750584457	snp	A/T	1.66109e-05	0.00288187	stop-gained	RNF152	GRCh38.p7	18:61815858	CAGCCCTCTTCAGCC[A/T]CAGGATATCACAGTG	220441
rs750594013	in-del	-/GGA	1.65086e-05	0.00287298	cds-indel	RNF152	GRCh38.p7	18:61816269	CGGGAGCTGCGACAC[-/GGA]GAAGCCGGGAGGCAG	220441
rs750625191	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866298	ACTCCCCACCAGATG[C/T]CTTATACACGGGGAC	220441
rs750691985	snp	C/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893433	CTGCTTTGGCGATTT[C/G]TCTACTCTCTCCAGA	220441
rs750694175	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818739	AACAACTTAAACCTA[A/G]GTAAGAAGGAACACA	220441
rs750708857	snp	C/T	3.29516e-05	0.00405891	synonymous-codon	RNF152	GRCh38.p7	18:61815963	GACAGTGCACACCCC[C/T]GACCAGGTGGAGCTT	220441
rs750710914	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830506	CAACCATTGTCCTAA[C/T]ATTTGTCTGGCTTAT	220441
rs750723774	snp	A/G/T	8.24659e-05	0.00642082	synonymous-codon	RNF152	GRCh38.p7	18:61816227	AGTGTGTGGAATGGC[A/G/T]ATGACAGCCAGGACC	220441
rs750725647	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61855775	TGAGCGCAGCTAGCC[A/C]GGCCAAGTGGACAGA	220441
rs750737323	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61851662	TCCAGACTGTCTGGA[C/T]ACCCAAATTCACCCA	220441
rs750890695	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823729	TAATACTGGTTGAAC[C/T]AGACAAAAGCAGCAC	220441
rs750892367	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810393	GCCCATGCCTGTAAT[C/T]CCAGCACTTTGGGAG	220441
rs750996196	in-del	-/TC			upstream-variant-2KB, nc-transcript-variant	RNF152, LOC105372159	GRCh38.p7	18:61894681	AGGACCTCGACGCCG[-/TC]TCTCTACCGTGCAAA	220441
rs751007772	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61835815	TGTTGGTATTGGTAT[G/T]GATACTAGTATAGTA	220441
rs751023139	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861505	GTTCACATAACAAAA[C/T]CACCCAAAGATGCAT	220441
rs751051923	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61850018	CTGGCAGGGACATAT[C/T]GGGGTGAATTAGCCA	220441
rs751054405	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813040	ACAAAATGAAGCCAC[C/T]GGAGGCTGCTTTCAG	220441
rs751057188	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895567	TGCAGTGGCGCGATC[G/T]CAGCTCACTGAAACC	220441
rs751108310	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61851297	CACTGAAGTCCTTCA[A/C]AAGGGTGTCCACTCT	220441
rs751122728	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888041	AGGAAGTCTATGTGA[C/T]GTTTGAGTAAGTTTC	220441
rs751185129	in-del	-/GAAA			intron-variant	RNF152	GRCh38.p7	18:61844090	AAGGAAAGAAAGAAA[-/GAAA]GAAAGAAAGAAAGAA	220441
rs751237342	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860485	CATCAGAGCATTGTT[A/G]CACTGCAACGCATTA	220441
rs751250577	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823808	GGCCTGGCCCTGCCA[A/G]CACAGCCCACTAGGT	220441
rs751302918	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61830720	GATGAAGGAGGAGGA[A/C]GAAGGCATGGAGATT	220441
rs751356302	snp	G/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893650	CCGGGAGGGGCCCTG[G/T]GGCAACTTCTAGGGC	220441
rs751428046	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831515	TATCTCCATAATAAG[A/T]ATATTCAACTTTCTA	220441
rs751463283	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61831795	TCTATTTTAAAAAGT[G/T]TCCTGTCAAATGGTA	220441
rs751468534	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810644	CAAGAGCAAAACTCC[A/T]TCTCATAAATAAATA	220441
rs751472922	snp	A/G	1.64999e-05	0.00287222	missense	RNF152	GRCh38.p7	18:61816304	TGGTGACACCGCGGC[A/G]CCAGGGGCACCGCAC	220441
rs751483335	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61845921	GGTGGGGCTTTGTGT[-/G]GGGGGGCGTGGTGAT	220441
rs751498635	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61876450	GAGAAAGTACACTCA[A/G]CCCACAAAAAAAAAT	220441
rs751523475	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847240	TAAAAGCAAAAATAC[A/G]TCTAACAGGGCAGCA	220441
rs751603173	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836018	AGATTACACCCATGA[C/T]TTAAAATAATACATA	220441
rs751608864	in-del	-/AC			intron-variant	RNF152	GRCh38.p7	18:61833556	ACCACAGAACCACAG[-/AC]ACACACAAACATGAT	220441
rs751649421	in-del	-/A	3.46879e-05	0.00416446	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815820	TCAACCCCTAAGTTG[-/A]GCACCCACAAGAGAC	220441
rs751745787	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61857023	TAATTAAGTAGTAAA[A/G]CAAGGAGAAACCAGC	220441
rs751823100	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61882505	GTGCTCTGTGCATGA[C/G]GTTACAGAACTGGCA	220441
rs751848984	in-del	-/TTTATA			intron-variant	RNF152	GRCh38.p7	18:61883329	AAAGGTTTCATTAAC[-/TTTATA]TTTATATTGTATAGC	220441
rs751854554	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61821180	CTGCGTACCATCATT[C/G]GTCAACAAAACCAAT	220441
rs751863039	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61846419	TCATTCAATCTCATC[A/G]CTACATTGAGCCTCT	220441
rs751893466	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853811	CACTTCCTTGAAGTC[C/T]CTTTTGCCATGTAGG	220441
rs751951951	snp	A/T	1.65053e-05	0.0028727	missense	RNF152	GRCh38.p7	18:61816138	GGCAGCAGCGCACGC[A/T]CCTTGGAGATGGGCA	220441
rs751969752	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61816911	ACATTTAAGCAAGCT[C/G]TGGGTCATCCTTCTA	220441
rs751975648	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817544	CAAAGCCCCTGTATA[C/T]CGAGGGCCATCTTTT	220441
rs751999686	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61878978	ATTTTCACGCACAGG[G/T]TAAGTGGGATTAGAA	220441
rs752044532	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61882423	GGAACACAGTGAACA[A/C]AGTATCTTGGTGTGC	220441
rs752070580	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61852729	GGGTGCTGCCTGGAC[A/G]TCAGGACTTTTAAAA	220441
rs752079480	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890075	ATTAGTAGTACATTA[C/T]AGGTGGGGGTAGGAC	220441
rs752088063	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61874316	CAAATATAAACCAAG[G/T]CATTGGTGATAGCCA	220441
rs752122390	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61842739	ATCATGGTGGAAGGC[-/A]AAGGAGGAGCAAGTC	220441
rs752163809	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827145	ATAAATTCCTCCTTA[C/T]AGTCTGAACTTTGGC	220441
rs752171164	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61864178	CCGGAGTCACAGACC[C/G]CACAGGTCAGGGGCT	220441
rs752176586	snp	A/C/T	9.90171e-05	0.00703561	missense	RNF152	GRCh38.p7	18:61816300	AGCTTGGTGACACCG[A/C/T]GGCACCAGGGGCACC	220441
rs752274534	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830821	GATGGAGGAAGCATT[C/T]TTGAGGGGTACAGCT	220441
rs752287616	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61853032	TAAAAAGTGGTAACA[A/T]CTATGTAGCACTTTG	220441
rs752293075	in-del	-/TGT			intron-variant	RNF152	GRCh38.p7	18:61831920	ATATAGTATTATGTG[-/TGT]GGGGGGGTGTGGGTG	220441
rs752325112	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61861557	ATCAAGTGAGGCATG[A/G]CTGTACATGTTACGC	220441
rs752334430	snp	C/T	1.66807e-05	0.00288792	missense	RNF152	GRCh38.p7	18:61816387	TTGCAGTCCAGCAAC[C/T]TGGGCCTGCGCCGGG	220441
rs752362913	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61851420	AAACACTTACCCAAG[C/T]GCCTGAGCTGCCCCA	220441
rs752389069	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858014	TATAATCTATTAAAA[C/T]AAATGAAGCAGAGCC	220441
rs752453917	snp	A/C	1.71419e-05	0.00292757	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815832	GTTGGCACCCACAAG[A/C]GACTTCCCTGCAGCC	220441
rs752477091	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61883528	ACTAACAATGTTAGA[G/T]CTCTACAAAGCCTGC	220441
rs752544235	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822416	TACAATAACAATTTA[C/T]TTTCACAAAATAAAA	220441
rs752712105	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870514	GCTTCAAACCCCTGC[C/T]GACTCTGTGGTTCCA	220441
rs752713242	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61837643	CATTCCACTTGCTCA[C/G]TTGTTCTTTTTATTT	220441
rs752743610	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61857115	AAGACACAGAATCTC[A/T]CTTTTTACTTTGTGC	220441
rs752774867	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864274	CTGACTGGCTATCAG[C/T]GGGGTTTCTCACAAC	220441
rs752808127	in-del	-/GAAAGAAAGAAAGAAA			intron-variant	RNF152	GRCh38.p7	18:61844078	AAGACAGAAAGAAAG[-/GAAAGAAAGAAAGAAA]GAAAGAAAGAAAGAA	220441
rs752824092	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61843205	AAAACTATTTTCTTT[G/T]CAACTCGTGCACACC	220441
rs752877393	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61846318	GTGTCATGTAATAAA[A/C]ACTCAAAGGTACAAC	220441
rs752911141	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811794	CTAGACACAATTTCA[A/C]AGTACAGATCATGCA	220441
rs752952045	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884319	TCTTACTTTTTAAAA[C/T]TCCAGTTCATAATGA	220441
rs752977067	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61848100	GTTTCATTTGGGGCT[A/G]CATTCCCAGCATCTA	220441
rs753062322	snp	A/C/G			intron-variant	RNF152	GRCh38.p7	18:61869630	TAGCTGATCCAGGAG[A/C/G]GTGCCAGGAAGACAC	220441
rs753192722	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61817588	TTTATAGCACCAACT[A/G]TGGGCCTTGAGTATT	220441
rs753195314	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61863364	CACTTGAACCTGGGA[A/G]GTGGAGGTTGCAGTG	220441
rs753200247	snp	C/T	1.64784e-05	0.00287035	missense	RNF152	GRCh38.p7	18:61815995	TCACCACGCCCCGCC[C/T]GTCCTGCTCCTCCTC	220441
rs753218340	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880105	CCTTCTAGAAACAAT[C/T]CACACCACCTGACTT	220441
rs753222817	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864791	AGTGCTCACGCCTGC[C/T]GAGGCAGGTGGATCA	220441
rs753227869	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61844120	GAAAGAAAGAAAGAA[-/AA]AGAAAGAAAGAAAGA	220441
rs753265504	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61817924	GGAGCCATGATGACT[C/G]TAGAAAGAATTACTC	220441
rs753277603	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61842319	AGTTTTCTAACTCAC[A/G]GCACAGTTCTATTAA	220441
rs753326343	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61854749	GGAGAAAAGAACCCA[G/T]TGCTGAATCATGGCC	220441
rs753396053	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61855393	CAGGGACGCCAGCTG[C/T]AGTGGGGGAGGCGCA	220441
rs753427504	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61889992	ACTTGAAATAGGCAA[A/C]GAGAGGATTATAATT	220441
rs753445886	in-del	-/A			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814587	TCCACTTATATTGGG[-/A]ATTTGAGCTGTTAGT	220441
rs753493062	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841781	TCTCAATCTCCAACA[C/T]GGCAGTAAATCACTA	220441
rs753556461	snp	A/C/T	3.30029e-05	0.00406209	missense	RNF152	GRCh38.p7	18:61816298	GCAGCTTGGTGACAC[A/C/T]GCGGCACCAGGGGCA	220441
rs753655305	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61837790	TCCTAACTTAGTGCT[C/G]TTCTTGATATAATTT	220441
rs753671757	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61886420	AGAACTGAGATCTCT[C/T]TGAGTGCCTATACAA	220441
rs753710136	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61871478	AAACCAGAACACAGA[-/G]GGGTCAGCAAGGATG	220441
rs753816067	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866244	CCAACCTACTGCTTC[C/T]AGACAGCGAGTCGGG	220441
rs753826980	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827514	AAAATATATATTTCT[C/T]TAAATTTCCTCAAAT	220441
rs753897944	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883237	ATAAATTGATGCCAC[C/T]ATTTCAATAAGTCTT	220441
rs753906059	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61891978	GCAGGACTCTGCCCT[C/G]TAGCAGAAAATGCTA	220441
rs753924848	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854862	CGTGAAAATAGCAGG[C/T]GGAAAAAAATCAATG	220441
rs753961700	snp	C/G	3.29772e-05	0.00406048	missense	RNF152	GRCh38.p7	18:61816042	GCCCCACCTTGCAGA[C/G]GCTGCTGTTCAGCAG	220441
rs754028214	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61829415	ACCAGAGCGGCTGTC[C/T]CTGCAGCTGGGATGG	220441
rs754037112	in-del	-/ATGG			intron-variant	RNF152	GRCh38.p7	18:61884959	CACCACCATAGGTGA[-/ATGG]ATGGATGGATCTGTA	220441
rs754114877	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61890937	AAAGAGGCATTAAAG[G/T]TGAGGCTGGATGACC	220441
rs754170956	in-del	-/GGGAAGGAG			intron-variant	RNF152	GRCh38.p7	18:61844193	AGAGGAAGGAAGGAA[-/GGGAAGGAG]GGAGGGAAGGAGGGA	220441
rs754172160	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61834833	GTTACTAGGTAGGTA[A/T]CTAAACTTAGATGTT	220441
rs754190623	in-del	-/CAC			cds-indel	RNF152	GRCh38.p7	18:61813307	ACACACACACACACA[-/CAC]ACACACATACACAAG	220441
rs754202082	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863921	TGGGTGGTGAGCTCC[C/T]GCTCTAATCGGCTGC	220441
rs754202638	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809405	ATTTCCTTCTGCTTA[C/G]AGCCCATGCTCTTCC	220441
rs754247290	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61837592	ACTATGGACTTATCT[G/T]CATCCCCATATAACA	220441
rs754254232	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808511	GCCATTAGACTGGAG[C/T]ATTTGTTATCAAGAG	220441
rs754260154	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824745	GAAAAGAAGCTGCAC[A/G]GTTTTCTGGCTTGTG	220441
rs754334831	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61817078	AACTTCACAAACCTA[-/G]GTACTTCCTATAACT	220441
rs754357584	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870720	ATGGACCTCATTTCT[C/T]TGGGCCCAGGAAGAA	220441
rs754369303	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844178	GAGGAAGGGAGGAAG[A/G]GAGGAAGGAAGGAAG	220441
rs754437225	snp	C/G/T	3.29876e-05	0.00406115	synonymous-codon	RNF152	GRCh38.p7	18:61816197	AAGTTTGATGAAGAC[C/G/T]GGGGTGTGTTCGGAA	220441
rs754455342	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61844986	TCCTCCTGAGGGCCA[C/T]AAGTGGACACGAGTG	220441
rs754485024	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61875719	ACCTGTGTATGTCTC[A/G]CCACTCATTCAATTA	220441
rs754516197	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61848782	CAGATGGGGACAAGG[C/G]GCTAAGGCAGGGAGG	220441
rs754516553	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61888102	TTATGCAGGCATTAG[A/T]ATATCAAGGGGTAAA	220441
rs754635987	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61824692	TCCTATTACCCAAAC[C/T]TGTTACCAGATGAAG	220441
rs754678692	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61850059	CCTGTCTCTTTTAGA[A/G]CTTCTTCTTTCTCAA	220441
rs754740522	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831638	ATAAGCAATTTAGAA[A/C]ACAATGCTCACTTCC	220441
rs754793571	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831796	CTATTTTAAAAAGTG[A/T]CCTGTCAAATGGTAA	220441
rs754810416	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61866362	CCTCATTGTCTTCTT[A/C]TTACACACCAGGAGC	220441
rs754813893	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61845431	GAGCAAACCACTCAG[A/G]CCGCCGCTGCTCAAA	220441
rs754829284	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61882628	CTAGAAGAACTGGTG[C/G]CTTGGCTAAGGGCCT	220441
rs754965451	snp	A/C/T			intron-variant	RNF152	GRCh38.p7	18:61840438	GGCTGTGGCACAGGG[A/C/T]AGAGGATGGGGGTGG	220441
rs754973993	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61867503	TCAGTCTGGTTTTTA[C/T]AGTTGTTTCCTGGGA	220441
rs754976855	snp	C/T	1.64776e-05	0.00287028	missense	RNF152	GRCh38.p7	18:61815989	AGCTTTTCACCACGC[C/T]CCGCCTGTCCTGCTC	220441
rs755041226	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837042	ACTTTAGCACCCTCA[A/G]TAATGGAAGAGCTGA	220441
rs755050128	in-del	-/CAG			intron-variant	RNF152	GRCh38.p7	18:61844067	AGAAAGAGAGAAAGA[-/CAG]AAAGAAAGGAAAGAA	220441
rs755060084	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889176	TCACTTGAATGAAGC[C/T]GGGTGGTCTCAACCT	220441
rs755065590	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61868267	TATGTCCCAATATTT[C/G]TCTTTTCCTCCTAGC	220441
rs755075623	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61873194	ATGAGAATGAAATTG[G/T]GTAACTTCTGCAGAA	220441
rs755100456	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61821923	ACCCATCCGTCCTGT[A/G]GAAAAATTGTCTTCC	220441
rs755109830	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61883329	AAAGGTTTCATTAAC[G/T]TTATATTTATATTGT	220441
rs755186907	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846565	CGTTGAGCACTTACT[C/T]CTTCCTTTCCCCGCA	220441
rs755194792	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809715	CAAATATTACTGATT[A/G]TCCCTAAAAATATCA	220441
rs755198418	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61872252	TCCACCCCCATGATC[A/C]AATCACCTTTCACCA	220441
rs755205854	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878443	CATTGTCCACTAACA[C/T]ATACCCTAAGCAATC	220441
rs755212221	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810645	AAGAGCAAAACTCCA[C/T]CTCATAAATAAATAA	220441
rs755279674	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61878986	GCACAGGGTAAGTGG[A/G]ATTAGAAAGAACAAA	220441
rs755304938	in-del	-/AC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808659	TGTTGAGTGAGGCAA[-/AC]ACAAACAAGTGGTGA	220441
rs755361346	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61868799	GCATAAATCAGTAGT[C/G]TGCCTTGTAGTTATG	220441
rs755434392	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890108	TATATTAGTAAATTA[C/T]AGGTTGGAATAGTAA	220441
rs755446098	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61852802	AGCTACAGAACATAA[A/G]GCACACACCTGCCTG	220441
rs755476042	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864195	ACAGGTCAGGGGCTC[A/G]GCCCCACAAGTCTGC	220441
rs755494071	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61860321	GAGGAATCATAAAAC[A/C]CTCCCGATTCAGAAG	220441
rs755495771	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61841858	TTTGCACAGGGACAG[A/T]TGGTAATATTTTAGG	220441
rs755588324	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61860150	TGGGGAAGGGAGGAA[-/G]GGTTCTCCCCATGGG	220441
rs755588777	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831662	CACTTCCTACTGTCA[A/C]TAGCTACCCTCAAAG	220441
rs755602560	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61816943	AATATACTAGAGAAA[C/T]TTTCCTGCTTCCAAT	220441
rs755621058	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841645	CTACCTCTGAGTGGG[C/T]AGAGATGCAGAAAAA	220441
rs755638341	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61894840	GACAGCGAGAGGGAG[A/G]AGCTGAGATCATCAG	220441
rs755664116	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61877719	GAATTATTGCAATAA[G/T]GCTGATGCTGCACAA	220441
rs755688355	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814490	GATAGGAATTTATCA[A/C]GTACTTGTAGCAGAT	220441
rs755780594	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61888785	CACAGTGTAACTCTC[C/G]AAGCCATGGGAAAAG	220441
rs755826917	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887878	GGTAGGTGGGAATGC[A/G]ATAGTGGCAGGGGAG	220441
rs755850531	snp	C/T			missense	RNF152	GRCh38.p7	18:61815938	AGACCAAGACGCAAG[C/T]CACCAAGATGACAGT	220441
rs755862173	in-del	-/TAATT			intron-variant	RNF152	GRCh38.p7	18:61869187	CTGACCACAAAACCC[-/TAATT]TAATTAGTAAAATCC	220441
rs755868207	snp	C/T	1.86897e-05	0.00305687	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816511	GTGAAGGGGAAGGAG[C/T]TGCTTCTCAGAGGCC	220441
rs755887043	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61867336	ATGCTCCTGTAGTCT[C/G]AGCTACTCGGGAGGC	220441
rs755929813	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61884515	GCTAGAAGGCAGGGA[G/T]TTTTTTAGAATTATG	220441
rs755950266	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61857132	TTTTTACTTTGTGCT[A/G]ATAATTCCTACCCTG	220441
rs755953745	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847334	GCTTTTGTGGGCGAC[C/T]TGAAACTTTCATTGC	220441
rs756002863	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61873478	AAGTAGCTGGGATTA[C/T]AGGCACGCCACCACG	220441
rs756097991	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817082	TCACAAACCTAGGTA[C/T]TTCCTATAACTAACT	220441
rs756138955	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61890170	TCAATCAATACTCTT[A/G]TGACATCCAATACCC	220441
rs756188444	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879176	ATACTAAATGGTTAC[C/T]TCCACTCCGAATGTG	220441
rs756224240	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61890829	AACAATGTAAGGACC[A/G]AACTGTATGGAATTC	220441
rs756290418	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61827436	TCTTGGCTCAATGAA[A/G]AAACAAACAACAACA	220441
rs756331633	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837665	TTTTTATTTCTAAGA[C/T]ACTTGATAGAAGAAA	220441
rs756346462	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863131	TTGCCCGTAAAACAT[C/T]TGCTCTTGAAAAGTA	220441
rs756374665	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61883137	TTCAAAGCCCACAGT[A/G]TTCAGCCCCTCAACC	220441
rs756379420	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811821	TGCATAGCTTGCAAG[A/T]CAAACGTTTTACAGG	220441
rs756379507	in-del	-/AAA			intron-variant	RNF152	GRCh38.p7	18:61844091	AGGAAAGAAAGAAAG[-/AAA]GAAAGAAAGAAAGAA	220441
rs756420780	in-del	-/G			frameshift-variant	RNF152	GRCh38.p7	18:61816277	CGACACGGAGAAGCC[-/G]GGGAGGCAGCTTGGT	220441
rs756440225	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61881298	CTATAGATTATAGCG[A/T]ACGACACCAGTCACC	220441
rs756518719	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61835490	CAATTAAGGGAAAGG[C/T]TCATGAATAAGGAGG	220441
rs756528064	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870587	GAAAGCTACCCCCTG[C/T]AGGTTTTCCACCAGG	220441
rs756566705	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61880175	TAGCCAGAAATCTTG[C/G]TGCAAATTTCCCAAC	220441
rs756608696	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61817626	TTTGGTATACATGGG[C/G]GTCCTGGAACCAATG	220441
rs756629226	snp	C/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892775	GACACCCAGGCGCTA[C/G]CCAGATCGTGGGGGG	220441
rs756635332	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61842846	AGGAAACCCATTCAC[C/T]ATCACAAGAACAGCA	220441
rs756725749	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896186	TTCAAGAGTCTTTAT[C/T]TTAAGCCCCAACTTC	220441
rs756739457	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811378	TAATTATTGTAGCTT[C/T]AGTAAACTTCAAGTC	220441
rs756744466	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61821837	ATCTAGACTGCACAC[C/T]CTTTATGAGGATCTA	220441
rs756776959	in-del	-/ACAG			intron-variant	RNF152	GRCh38.p7	18:61844126	AAGAAAGAAAGAAAG[-/ACAG]AAAGAAAGAAAGAAA	220441
rs756899309	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841782	CTCAATCTCCAACAC[A/G]GCAGTAAATCACTAA	220441
rs756903226	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61890445	GATCTTGCAAGCTCA[C/G]ATCAAGACCAAGACT	220441
rs756912242	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61816809	ATGGCAAATACTTAG[G/T]TCATTTCTAAAAAAA	220441
rs756921077	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61867816	AAAATGTAAAATACT[C/G]CTCTTAAATCCTATA	220441
rs757009645	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871485	GAACACAGAGGGTCA[A/G]CAAGGATGAGTAATT	220441
rs757076949	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61847452	ACTCAGAAAAAATTC[C/G]CGCAAGTGTCCTTGA	220441
rs757112083	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61875548	AAGCCTCACATTCAT[A/T]ATGACCATCTGGGCG	220441
rs757113324	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822635	ATCCAGATAGTTTTA[C/T]TCTGCTTACACTCTT	220441
rs757123377	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61837791	CCTAACTTAGTGCTG[G/T]TCTTGATATAATTTC	220441
rs757144642	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884997	TTTCTGAAGTACCAA[C/T]GTAAAGGAGTGGAGT	220441
rs757170972	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837230	AAAACAAAAAGCAAC[A/G]AGATTGTTCTAGATT	220441
rs757183937	snp	A/G	1.65002e-05	0.00287225	synonymous-codon	RNF152	GRCh38.p7	18:61816311	ACCGCGGCACCAGGG[A/G]CACCGCACATCCTTC	220441
rs757262595	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880295	TGTTCCCAAAGACAG[A/G]TCCGCAAAGAATTCA	220441
rs757293272	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885248	AAAAGAATATCACAA[C/T]AAATACTTGGTTCCT	220441
rs757330453	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827541	AAATTACCCAGAGAA[C/T]ATTCTATATTAACAC	220441
rs757364051	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864975	CAGTGAGCTGAGCTC[A/G]TGCCATTGCACTCCA	220441
rs757379623	in-del	-/ACCCACA	3.46654e-05	0.00416311	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815823	AACCCCTAAGTTGGC[-/ACCCACA]AGAGACTTCCCTGCA	220441
rs757451957	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854863	GTGAAAATAGCAGGC[A/G]GAAAAAAATCAATGT	220441
rs757463417	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61844382	TAAAATCTCACACAA[C/T]AAACCTGAGAGGAGT	220441
rs757464952	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828473	CATGTTGCCCAGGCT[A/G]AAGTGCAGTGACACA	220441
rs757511212	snp	G/T	1.65023e-05	0.00287244	missense	RNF152	GRCh38.p7	18:61816081	ACCACGGTGACGGAC[G/T]TCTGCTGGCTCCCGG	220441
rs757513139	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824777	AGGAAGCCAAGGTTA[A/G]CGCTGGCATTCATCA	220441
rs757529060	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61836013	CCATCAGATTACACC[C/G]ATGATTTAAAATAAT	220441
rs757584011	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837628	CCTCATACAGATCTC[C/T]ATTCCACTTGCTCAG	220441
rs757622154	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61850340	TCCTTGAATGCAGAA[C/T]GCTATCATTATCACT	220441
rs757701037	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61888179	AACTCCACGAAGAAC[A/G]TAGTCCAGGCCTTAG	220441
rs757712970	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61871022	CCTGCTTCCCAGAGA[C/G]GCTGTTACTAGAATT	220441
rs757823795	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61834110	TCCAATCTTATTTTT[C/G]TTACGTCCTGGCTTG	220441
rs757850898	in-del	-/ATAA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810652	AACTCCATCTCATAA[-/ATAA]ATAAATAAATAAATA	220441
rs757866297	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823622	ATTTAAGATGTTTAC[A/G]TATTTAAACAGGGAA	220441
rs757885992	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812290	TGGTGGCTACCGTAC[C/G]AGACGGCACAGGTTT	220441
rs757910528	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61885434	TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA	220441
rs757952418	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61835401	TACGTGAAAGAGTTC[A/C]CCTTATTTCAAGGTG	220441
rs758064806	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61858851	TCACAAAAACAGAGA[A/T]CCCGTTTTAATAGGA	220441
rs758148365	snp	C/T	3.41186e-05	0.00413015	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815836	GCACCCACAAGAGAC[C/T]TCCCTGCAGCCCTCT	220441
rs758150186	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61849656	AATGGATCTCTCCTC[C/T]ACCAATTAGTTTGAA	220441
rs758152732	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859485	CAGGAGATGCTGCCC[C/T]TGAAGAAGGGCCTGG	220441
rs758162318	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61865123	TACCAGGAAATGGAG[C/G]ATGAAAACCAAATAT	220441
rs758244253	snp	C/G/T			intron-variant	RNF152	GRCh38.p7	18:61866315	TTATACACGGGGACT[C/G/T]GTTTATCCTCAGGAC	220441
rs758281406	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61892108	TCCTTGGAAAGAAAA[C/G]AACAGGCCAGAGTTT	220441
rs758368281	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61839240	ACATTTCACCCAGTG[A/T]TCCTCTAATAATGCA	220441
rs758389027	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61871306	TTCCTCTGGGCCTGC[C/T]TCTGGATTCCCACCT	220441
rs758542953	snp	C/G/T			intron-variant	RNF152	GRCh38.p7	18:61846392	TACCCACTGTGCCTA[C/G/T]GCAATCTCATCTCAT	220441
rs758570766	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61845214	CATCAGCCTCCCAAA[A/G]CAATGGGATAATAGG	220441
rs758600237	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61835111	TAGCAAGGAAATGTG[G/T]CATTATCTAATAAAG	220441
rs758649217	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893525	CGAGCAGCGCCCCAC[A/G]AGTCCAGCTGGCTTT	220441
rs758651147	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61881599	AATCAAATGAATGCT[A/G]AAGCAACTAGAACTA	220441
rs758674841	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888977	GCATTTTGGGGCTTC[C/T]CAAATATAGTTCAAG	220441
rs758681194	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61819620	AGGAAGGTAATATCA[G/T]TATGAGAAATAGGGA	220441
rs758696916	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877776	TTTTTGTGTTTGGAA[C/T]CTCTATTTTTACTCA	220441
rs758721105	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61872428	TAACAATGCTTGTTT[-/A]AAAAATCTTACTATC	220441
rs758738509	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61821888	GGTGGAACAGTTTCA[A/T]CCTGAAACCATCGGT	220441
rs758792464	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890042	GTACAACCATGTTAG[C/T]AAATACCATATCAAC	220441
rs758812188	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841028	TTCCTACCACCTACT[A/G]CAGGAGGCTGGCATG	220441
rs758812265	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852709	TTCTGATTCAATTGT[C/T]TTGGGGGTGCTGCCT	220441
rs758841185	snp	G/T	1.64781e-05	0.00287033	missense	RNF152	GRCh38.p7	18:61815996	CACCACGCCCCGCCT[G/T]TCCTGCTCCTCCTCC	220441
rs758862741	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61862901	CTCAATCAGTGGGCT[A/C]TGACATTATCTCTGG	220441
rs758971013	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61835885	CAAATAAGCAACCAG[A/C]TTGATATTGTCAGAA	220441
rs758971163	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61824940	GATAAAAGATGCTGA[C/G]AGATAGACAGACAGG	220441
rs758987393	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825913	GAAACCTTAAGTCAA[C/T]TTGTTGGCTTTTTAA	220441
rs759006142	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825732	TGGAGAGCAAAGGTC[C/T]CTCTCTGCTATAGCC	220441
rs759049933	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823006	AGTTATATTGGATCT[C/T]AGCAAACACTCCAAT	220441
rs759099158	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846109	TCCCAGCCTCCAGAA[C/T]TGTGAGTAATAAATT	220441
rs759115026	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61821134	CTTGGGAGGAGGCAT[G/T]CAAGTGTTCTTCCTG	220441
rs759123508	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61835431	GAAAGAGTGAGAATA[C/T]ATATTTGTTTATTTT	220441
rs759131205	in-del	-/CACACACAC			cds-indel	RNF152	GRCh38.p7	18:61813307	ACACACACACACACA[-/CACACACAC]ATACACAAGAATGCA	220441
rs759135708	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61862369	CAGGGACTGCCCAGA[A/G]AGGAGATGACCATCC	220441
rs759352071	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831522	ATAATAAGAATATTC[A/C]ACTTTCTAAGGAGCC	220441
rs759372919	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61868912	ATCCACACATCTTCA[-/T]AGATGACTTAAAATC	220441
rs759398604	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833258	CAAGAATCAGATTAA[A/G]TTGGTTTATTGAGAC	220441
rs759408443	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61853423	GCCTCCTGAGTAGCT[A/G]AGACTACAGGCACAT	220441
rs759458923	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877637	ATCACACGTCAAAAT[C/T]ATTAGGGTGGTAGGA	220441
rs759465828	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823301	AATTGTCGTTTAAAC[A/G]TGTTTTTTGTTTTTT	220441
rs759489107	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61889646	TGTGACCAGAAAAAG[C/G]CTCTTGCCCAAATTG	220441
rs759490351	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61891779	TCAAGTTTTTAACTT[A/C]ATTTTTCAAGGGATT	220441
rs759501990	snp	C/T	8.67611e-05	0.00658582	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815818	TGCTCAACCCCTAAG[C/T]TGGCACCCACAAGAG	220441
rs759516152	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852476	TCATACACTGATCTG[C/T]GTATATCATTGAAAG	220441
rs759593707	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811680	TTATATTTGCACCTT[A/G]CTAATACAGCAATGA	220441
rs759594425	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61885911	TGGGGTGGTCTGGTA[G/T]GCTGTAAAGTCCTAA	220441
rs759632759	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884261	CAGTCAGACCTTGTG[C/T]ACTCAGGTCACGTGG	220441
rs759648215	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61816951	AGAGAAACTTTCCTG[C/T]TTCCAATAAGTTCAT	220441
rs759676143	snp	A/G	1.651e-05	0.0028731	missense	RNF152	GRCh38.p7	18:61816126	CCCATGTCTCCGGGC[A/G]GCAGCGCACGCTCCT	220441
rs759679637	snp	A/G	1.64904e-05	0.00287139	stop-gained	RNF152	GRCh38.p7	18:61816046	CACCTTGCAGAGGCT[A/G]CTGTTCAGCAGGGAT	220441
rs759699726	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870385	TGTCCTCATCTCCCA[C/T]GTGGTATTTTCTTAC	220441
rs759764341	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847266	CAGCAAGCTTTAACA[C/T]ACAAGCAAATTGGGG	220441
rs759778914	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61859165	CAGACTGGGACAAGT[A/C]TGTACTTGCTCAAAT	220441
rs759798634	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61832613	TAGTCATGAAAAGTA[C/T]CTAACATCAATAAGT	220441
rs759892464	in-del	-/AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA/AG			intron-variant	RNF152	GRCh38.p7	18:61844098	AAGAAAGAAAGAAAG[lengthTooLong]AAAGAAAGAAAGAAA	220441
rs759901876	snp	C/T	1.65485e-05	0.00287645	missense	RNF152	GRCh38.p7	18:61816355	TCTGCTGCAGGCACA[C/T]TGAACAGCAGGTGTG	220441
rs759917422	in-del	-/T/TT			intron-variant	RNF152	GRCh38.p7	18:61853296	TCTGGTTCCTTGCCC[-/T/TT]TTTTTTTTTTTTTTT	220441
rs759941104	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844118	AAGAAAGAAAGAAAG[-/AG]AAAGAAAGAAAGAAA	220441
rs759952110	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837578	GTATTTTTTTAATTA[C/T]TATGGACTTATCTGC	220441
rs759964795	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891866	TAAAAGAGAGTAGAC[C/T]AGGAGCCTTTGGCCC	220441
rs759981681	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61854723	TCTCTCTCCTTTCAC[A/T]AGCACATCAGGGAGA	220441
rs760096212	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61838484	TAACATTAGCAGAAA[G/T]GAATCTCAAAGAACC	220441
rs760165685	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61827921	TAGATATGGAACAGC[A/G]GTGCAACCCAACACC	220441
rs760181142	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873911	TTTGTTGAGGCTGAT[A/G]GAGATGAAATTTTAT	220441
rs760239805	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889963	AATGGCCTTTCACTT[C/T]AGAGTAAACATGCAC	220441
rs760329633	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61878588	CAACAAAATACTTGT[A/G]ATTGGGTGATTTATA	220441
rs760372856	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836505	GATCAGTGCCCTCTC[C/T]CTCTCCTGCCAAGTG	220441
rs760436516	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859333	GGGCTGTTGTGGCGC[A/G]AATTCAAACTTGACG	220441
rs760445304	in-del	-/CCTCAAGTAATCCACCCG			intron-variant	RNF152	GRCh38.p7	18:61885538	GTCTCAAACTCCTGA[-/CCTCAAGTAATCCACCCG]CCTCAGCCTCCCAAA	220441
rs760505491	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61822470	ATTTTATGCATCTTT[A/T]GAAAAGGTACAGGTG	220441
rs760563089	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61869422	GTCTCCTGCACCTGA[A/C]AAGAGATTCTGTTAC	220441
rs760591645	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893747	ACTGGGGCGGGCGCG[C/T]GCGCACGTGCACACC	220441
rs760630189	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61879589	TACACAAAGGAATGG[G/T]AATACAAAAGGGTAT	220441
rs760665455	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61818802	TTCAAATTTTCATTG[-/C]ATATCTACTATGTGT	220441
rs760777779	snp	A/G/T			intron-variant	RNF152	GRCh38.p7	18:61875311	TGTAAAATCTTTTCA[A/G/T]TATTTTAAATCCAGT	220441
rs760794313	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61856367	TTAATTTTAAAGATG[-/C]CTGTTGGGAACTCAT	220441
rs760902436	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61886191	TGCAAGTAGGGGAAG[C/T]TCTTAAAAATAAGTT	220441
rs760910068	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61829214	CTAGCGAATATCACT[G/T]TAAGGGGAGGCAGGA	220441
rs760939402	snp	A/G	4.94279e-05	0.00497107	missense	RNF152	GRCh38.p7	18:61815964	ACAGTGCACACCCCC[A/G]ACCAGGTGGAGCTTT	220441
rs760951499	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860189	GTGCATGGGCCTGCC[A/G]ACACCATGCCTGTGG	220441
rs761047821	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812888	AGCAATAGTTGACTC[A/G]GTAAAGGGTATTCAT	220441
rs761071149	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893162	CTCTGGTGGCAGAGC[A/G]CCTACTAGCAACAGT	220441
rs761088343	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61867607	GAGGGAGAGCACCCA[C/G]TATTGATGAAACTGT	220441
rs761143169	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818395	ACCACTGCACTCCAG[C/T]CTGGATGACAGAATG	220441
rs761168934	snp	A/G/T	3.30291e-05	0.0040637	missense	RNF152	GRCh38.p7	18:61816334	CATCCTTCTGGCTGG[A/G/T]CCTCATCTGCTGCAG	220441
rs761193983	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809941	AAATTGCAGGGATTC[A/G]GGAATAATGGTGCAC	220441
rs761197105	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866122	AGGGAATTTGGAGGG[C/T]TGAGTGGCACAGGGC	220441
rs761228025	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830290	CTCGTCCTCCCAAAG[C/T]GCTGGGATTACAGGC	220441
rs761241229	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884125	TTAGCAACAGCTGCC[A/G]TTTATTTAGTCTTAC	220441
rs761242262	in-del	-/TTTAG			intron-variant	RNF152	GRCh38.p7	18:61865639	CATCCCGTTGTGGAA[-/TTTAG]TTTAGAGTCTCTGTT	220441
rs761303789	in-del	-/TTTTT			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896219	GGCAGGAAGGAGAAT[-/TTTTT]TTTTTTTTTTTTTTT	220441
rs761366570	snp	A/G	0.000111088	0.00745197	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816496	AAGGGCAAGGCCAAG[A/G]TGAAGGGGAAGGAGC	220441
rs761439319	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61881100	TGTATTTTTAGTAGA[C/G]ATAGGGTTTCCTCAT	220441
rs761451901	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61824390	TGCTGGGTTTCCAAC[C/T]GCATGGCAGTACTGC	220441
rs761466857	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854617	TTTGAACGAGGTATT[A/G]TTTAAGCTGGGGTAA	220441
rs761471286	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61869475	TGCCCTGTCACCTCA[A/C]CACAGACGGCACTAA	220441
rs761529245	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61839794	CAGCTACTCGGGAGG[-/C]TGAGGCAGGAGAATG	220441
rs761540095	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61828050	ATCAGCAATAAAATG[C/T]ACATATGTTCAGTGT	220441
rs761552013	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61849658	TGGATCTCTCCTCTA[C/T]CAATTAGTTTGAAAG	220441
rs761557041	snp	C/G			upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61894486	GGGGGGAGAGGCTGG[C/G]CTCCGCTCCCCGCGG	220441
rs761573259	in-del	-/CACACACAC			cds-indel	RNF152	GRCh38.p7	18:61813303	ACACACACACACACA[-/CACACACAC]ACACATACACAAGAA	220441
rs761624124	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61862502	CATGAGGGGATCCCA[C/T]CCTGTGCCCTGGGGA	220441
rs761638245	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812992	GAAGTTCATATCCCC[A/C]CCTTTCTGCAGAATT	220441
rs761676212	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808423	AAAAAGCTCCTAAAA[A/T]AAATAATCCACATAA	220441
rs761698166	in-del	-/ATAA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810649	GCAAAACTCCATCTC[-/ATAA]ATAAATAAATAAATA	220441
rs761717367	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61834454	CCCACACTGAAAAGT[A/G]AGTTCCTTAGAGGGA	220441
rs761724164	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813934	ATTCAGCTAATATGA[C/T]ACCTAAATTATTAAT	220441
rs761776728	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61851993	TCCCTATGACATATA[-/T]GAGGCAAATGACGTC	220441
rs761843352	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61830380	ACTCATTCAACAACC[A/G]CTCCCCATTTCTCCT	220441
rs761861429	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61860326	ATCATAAAACCCTCC[C/T]GATTCAGAAGCAGCA	220441
rs761868384	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823578	TGCTGGGATCACAGG[C/T]GTGAGCCACCACGCC	220441
rs761927942	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61838823	CTCATGACTTGACTC[A/C]TTGACTCCCTCCTTT	220441
rs762003095	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61855759	GGCTGGTAGCATGAA[C/T]TGAGCGCAGCTAGCC	220441
rs762029679	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831722	ACTGTAAATACAATT[A/T]CTATGTCAGATAGAA	220441
rs762057766	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61877468	ACTGTTCCCAAAAAA[G/T]GTTAAAATGCATTAT	220441
rs762080681	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61850860	CTGTGAGGTACACAC[A/G]TACTCAGGAAGCTCC	220441
rs762131385	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866251	ACTGCTTCTAGACAG[C/T]GAGTCGGGCCCAGGT	220441
rs762137373	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61856916	AATAGTGTCACCTAA[-/G]CGTTATTTACAAGCA	220441
rs762153885	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61887057	AAGAAAGAGGCAATG[A/C]AAAACATTTTGGGCA	220441
rs762167768	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815112	TGGCTTGAGGAAAAT[C/T]GGCATACAGGTTTTC	220441
rs762180556	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810309	TAGTAAGTCAGTTGT[A/G]TCAGAAAAATCAATG	220441
rs762185297	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61840437	GGGCTGTGGCACAGG[A/G]CAGAGGATGGGGGTG	220441
rs762204859	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882922	TGTTCCAGAGGCATC[C/T]TAGCTTCAAACAAAA	220441
rs762287367	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61831189	TTAGAAGCGGTTCTG[C/T]GCACCAGGCTGGAGC	220441
rs762371552	snp	G/T	1.66902e-05	0.00288874	synonymous-codon	RNF152	GRCh38.p7	18:61816389	GCAGTCCAGCAACTT[G/T]GGCCTGCGCCGGGGG	220441
rs762375021	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820901	CAAAGTCATTTACCT[C/T]CTCTGAGCCTGCTTT	220441
rs762388013	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61865419	GAATTTGAAAGGAGA[C/T]TGCTTCCAGGATAAA	220441
rs762425086	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846230	TCTCTCTTGTTCTTG[C/T]CTTTTCCTCAATCTT	220441
rs762490861	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809119	CTTGTTTTGCAGCTA[C/T]ACTCTTCCTTTATTA	220441
rs762498153	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61855546	CAGATGTGGATGCCC[G/T]CAGTAGAAGCCACGT	220441
rs762541388	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870456	AGAAAGAGGAGACCA[C/T]GCCTGTCACCTTACC	220441
rs762578041	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61837195	ACTGGCTCCTCAAAA[A/C]TCTCAATGTCATGGA	220441
rs762587634	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815181	TGCTCCCCTGTTGAG[A/C]TTTCAGTTCCATAAA	220441
rs762650469	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61843918	TGTATTTACCACCAC[C/T]GAACTGTATACTTAA	220441
rs762652651	snp	A/C	1.83852e-05	0.00303188	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816486	CGTGAGCAGGAAGGG[A/C]AAGGCCAAGGTGAAG	220441
rs762668255	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818336	GCTGAGGTGGGAGGA[C/T]CACCTGAGCCTGGGA	220441
rs762750088	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61876754	CGTCTACTCTACCCC[A/G]TAGGATTGCTGTGAG	220441
rs762750221	snp	A/G	1.64781e-05	0.00287033	missense	RNF152	GRCh38.p7	18:61815958	AAGATGACAGTGCAC[A/G]CCCCCGACCAGGTGG	220441
rs762760151	snp	G/T			downstream-variant-500B	RNF152	GRCh38.p7	18:61807933	TCCACTTAAAATCCT[G/T]GGCTCAGGATCTTCT	220441
rs762791163	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61877569	AACTGCCAGTACACT[A/T]GAGGTTTTATTACTT	220441
rs762792930	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61840289	AAGCCACCCAGTCTA[C/T]GGTATTTTGCTATAG	220441
rs762813217	in-del	-/CACAC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813305	ACACACACACACACA[-/CACAC]ACACACATACACAAG	220441
rs762902702	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61888019	TTTGCATGAAAGGCA[A/G]GTAACCAGGAAGTCT	220441
rs762921386	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831747	ATAGAAAGCAATAAT[A/T]CATTTAATTAAAAAT	220441
rs762932881	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61825494	GAAGGACAGTGGCAT[A/T]TCCTCTATTTGATTA	220441
rs762942913	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854171	ACAGTTAACAAGAAG[C/T]GTTTTTCCTTTCACT	220441
rs762943373	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61861476	GGCTTGTGTAAGTGT[A/T]CTCACTCCATAATGT	220441
rs762983295	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61857664	AGCAGATAACACAAG[C/T]TCCATATCCTCCAGG	220441
rs762993287	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61850968	TTTCATACATGATTG[G/T]CTGTGTAGCCAATCA	220441
rs763003011	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814170	GTTTTATTTCACATT[A/T]ATTCCATCACTTTTA	220441
rs763025319	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61820949	GATGATGGAGTTGTG[G/T]CTGAAGGTCAAGTGA	220441
rs763091689	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61867221	CAACACTTCGGGAGG[A/C]AGGTGGATCAATTGA	220441
rs763135972	snp	A/G	3.29853e-05	0.00406098	missense	RNF152	GRCh38.p7	18:61816210	ACCGGGGTGTGTTCG[A/G]AAGTGTGTGGAATGG	220441
rs763187401	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61883258	AATAAGTCTTTACTG[A/T]GTGTCTACTGTGTAC	220441
rs763250587	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61844970	ATTTTATTCCTTCCA[C/T]TCCTCCTGAGGGCCA	220441
rs763258130	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61856844	GCCCAGGAAAAAAGC[A/G]ACAGGAAAATTGAGG	220441
rs763298916	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61831342	CATCATCTTTCCCTT[C/T]GCTGCTTATTTAGCT	220441
rs763323696	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890961	GATGACCATATTTTC[C/T]CTCCCCAGAAGTCCA	220441
rs763332513	in-del	-/TTTTTTTTT			intron-variant	RNF152	GRCh38.p7	18:61885987	TTTCTTTTGCTTTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT	220441
rs763340815	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837489	GTCATGATGTCTGCC[A/G]ATAAGATGAAATGTT	220441
rs763348649	in-del	-/TTG			intron-variant	RNF152	GRCh38.p7	18:61842151	TTGATCATATTCACT[-/TTG]TTATTTTCTTAACCA	220441
rs763420840	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864049	ATCTGTTTCTACCCA[C/T]AGAACATTTCTGACA	220441
rs763500121	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884166	GCAACACACTAAGCA[C/T]TTTATATGTAAGTCT	220441
rs763517718	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811616	CGACAAGCTGGCCAA[C/T]TTCAAGGGCAAACAA	220441
rs763518731	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847813	GCCTGGCCTTCACAC[C/T]TACTCTTCCCTCTGC	220441
rs763543531	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61874245	CAGTTTAACAGCGCA[C/T]GAACTGACCAAAGAG	220441
rs763632358	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878600	TGTGATTGGGTGATT[C/T]ATAAATAATAAATAT	220441
rs763691551	snp	A/G	1.67742e-05	0.002896	missense	RNF152	GRCh38.p7	18:61816397	GCAACTTGGGCCTGC[A/G]CCGGGGGCTGTAGTA	220441
rs763717954	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879601	TGGGAATACAAAAGG[A/G]TATGATTTATTCCAC	220441
rs763720189	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61868215	TACAGCATATATCTG[G/T]GTTATGTTTCAGGGA	220441
rs763808644	snp	C/T	3.29516e-05	0.00405891	synonymous-codon	RNF152	GRCh38.p7	18:61815960	GATGACAGTGCACAC[C/T]CCCGACCAGGTGGAG	220441
rs763827007	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61857312	AGCCCAGATCTTCAA[C/T]GCCTGCTCTGGAAAC	220441
rs763870426	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61832703	GGCATGCATTTTGTA[A/C]GCAGAAAATCATTAC	220441
rs763880206	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859827	GAGGTTGCAGTGAGC[C/T]GAGATTACACTATTG	220441
rs763905504	in-del	-/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809752	GAATAATATAAAAAA[-/C]CTTAGATTAGAATAA	220441
rs763940865	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859347	CAAATTCAAACTTGA[C/T]GTGCTTCAGAAACGT	220441
rs763955411	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61848156	ACCTGATTTCAAAAG[C/T]GCCTCTGGGCTCCTC	220441
rs763982776	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858341	TCCCCTGGAACCATA[C/T]ACCCTAGGATGAGGA	220441
rs764001565	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893829	CAGGGGGCATCCGAG[A/G]ACTCGGCCGAGCAGC	220441
rs764023382	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811864	ACTATTTTTGGACAA[C/T]AGGTTAACATGCAGC	220441
rs764044265	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61844870	ATGGCCTTTTAAAAC[-/A]AAAAAAAAAAAAGCA	220441
rs764078818	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864880	AAAAAATTAGCCAGG[C/T]GTGGTGGCGCGTGCC	220441
rs764129014	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61838583	TTCCTCTGAAGTCCC[C/T]GGCAATCCTCCAACT	220441
rs764201120	snp	C/T	1.64944e-05	0.00287175	missense	RNF152	GRCh38.p7	18:61816223	CGGAAGTGTGTGGAA[C/T]GGCGATGACAGCCAG	220441
rs764232219	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61876195	TCACGGGCATTGTCA[A/C]ATACTACATTTTTTG	220441
rs764259662	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61837668	TTATTTCTAAGATAC[A/T]TGATAGAAGAAAGCC	220441
rs764352609	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844125	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs764380354	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61863382	GGAGGTTGCAGTGAG[C/T]GGCGATCGTGCCACC	220441
rs764418657	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809362	GAGGTATCAACTAGA[C/T]CCCCTTTAAGAGGCA	220441
rs764437518	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61870678	AGAAAGAAAAAGGAT[C/T]GAGGTCCTATTTTCC	220441
rs764531476	in-del	-/TTTT			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896220	GCAGGAAGGAGAATT[-/TTTT]TTTTTTTTTTTTTTT	220441
rs764541600	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61819339	GCAGCCCCCAGTGCC[A/C]GGCCAAGGATTCAGG	220441
rs764574457	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61865940	CAGGCACTAGAGTCA[C/T]CATGTTGTCCAACAG	220441
rs764602229	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818661	ATTTATGGAATATCT[A/G]TTATGCACAAAGCAC	220441
rs764619700	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844122	AAGAAAGAAAGAAAG[-/AG]AAAGAAAGAAAGAAA	220441
rs764634130	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61881300	ATAGATTATAGCGAA[C/T]GACACCAGTCACCTG	220441
rs764690933	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808297	AACAGCAGCTTGATA[A/T]CCCCTTTACGAAGTC	220441
rs764692741	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61843627	TATTCAGCCTTAAAA[C/G]AGCAGGAAATTCTGA	220441
rs764702271	snp	C/T			downstream-variant-500B	RNF152	GRCh38.p7	18:61807798	ATGCAGCACAATTTC[C/T]AAACACTGGAGGATA	220441
rs764706901	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61832968	ATGGAAAATCTGTAT[C/T]TGCTTAATTCAAGAT	220441
rs764716205	snp	A/G	6.60251e-05	0.00574528	missense	RNF152	GRCh38.p7	18:61816136	CGGGCAGCAGCGCAC[A/G]CTCCTTGGAGATGGG	220441
rs764729550	in-del	-/CAA			intron-variant	RNF152	GRCh38.p7	18:61880766	TTTTAATTATGAAGC[-/CAA]CACCACCATATAAAC	220441
rs764838863	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869482	TCACCTCACCACAGA[C/T]GGCACTAAAGGTGAA	220441
rs764894814	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61854648	TCAGAAGGTAGTGAC[A/T]ACAATTTTCAGTTTT	220441
rs764946852	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875562	TAATGACCATCTGGG[C/T]GTGGATTACCCACGA	220441
rs764957226	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61871857	TAGTAAGCCTCTGAT[-/A]GGTACATATCTTCAT	220441
rs764985503	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879842	TGGTGGCGCACGCCT[A/G]TAACCCCAGCTACTC	220441
rs764986744	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815822	CAACCCCTAAGTTGG[C/T]ACCCACAAGAGACTT	220441
rs765024702	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837129	CACGCCTAAATGTTC[A/G]TCTTGCATCCAGTCA	220441
rs765031738	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823579	GCTGGGATCACAGGC[A/G]TGAGCCACCACGCCC	220441
rs765057058	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61849814	TCAAACCATCCTCCC[A/G]CCTCAGCCTCCCAAA	220441
rs765071020	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61849415	TCAAAAGTGTCACAG[A/G]TGGCCAATCCCTGAG	220441
rs765130582	snp	A/C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813996	ATGCCCAAGAGCTTA[A/C/T]ACAATAAAATGGCAT	220441
rs765145085	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61838948	CAATATTAGAAACTG[A/C]CCATTCACTCTCACC	220441
rs765190411	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61850905	CATGCACCCCTGAAT[A/G]GCTAGTGCAGCTCTG	220441
rs765219931	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61855761	CTGGTAGCATGAACT[A/G]AGCGCAGCTAGCCAG	220441
rs765223183	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860348	GAAGCAGCACCAAAT[A/G]GCAAAGAGAAAATGC	220441
rs765255201	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61824394	GGGTTTCCAACCGCA[C/T]GGCAGTACTGCCAGG	220441
rs765343186	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867032	TTTTTTTCTCACCAA[A/G]CATCAAACATTGCAA	220441
rs765349669	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893346	TCTTTCTTTCGTTTG[C/T]CCCTGTCCGCCACCT	220441
rs765361524	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61856779	CTCTGGGGATTCAGT[G/T]CCCCGAACAGCTAGC	220441
rs765373272	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831723	CTGTAAATACAATTT[A/C]TATGTCAGATAGAAA	220441
rs765410962	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866275	CCCAGGTAGCCCCAC[A/G]GATGGCTACTCCCCA	220441
rs765419473	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866262	ACAGCGAGTCGGGCC[C/T]AGGTAGCCCCACGGA	220441
rs765453540	snp	C/G	1.65094e-05	0.00287305	synonymous-codon	RNF152	GRCh38.p7	18:61816128	CATGTCTCCGGGCAG[C/G]AGCGCACGCTCCTTG	220441
rs765580366	snp	C/T			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868182	GTAGAGGTTGGCCTT[C/T]GGGTGTTGCTGTAGA	220441
rs765588911	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61825850	TGAACTACACATGTT[A/C]CCTACTCCTAATTTT	220441
rs765606015	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810079	ACAGTAGAACCTACC[C/T]CTTCATATATTTGAA	220441
rs765674375	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61835729	ACAAGCACTCCATAC[G/T]CCTTTAGTGGGGTAC	220441
rs765709575	in-del	-/AAAAAAC			intron-variant	RNF152	GRCh38.p7	18:61818445	AAAAAAACAAAAAAC[-/AAAAAAC]AAAAAACAAGAAAAA	220441
rs765709843	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61883011	TCATGAAGAGCATCA[A/G]CTCATACATAAACAC	220441
rs765738948	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810354	TTATCTTTTAGAAGT[A/G]TTTCATGTTGGCTGG	220441
rs765764665	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809515	AACTCCTGTTAGAAT[A/G]ACCCAATAACTCACA	220441
rs765788909	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61846280	AAACAATCCCAAAAA[A/G]CTGTCTTTGGGGAGC	220441
rs765842810	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888036	TAACCAGGAAGTCTA[C/T]GTGATGTTTGAGTAA	220441
rs766044174	snp	C/T	3.29864e-05	0.00406105	missense	RNF152	GRCh38.p7	18:61816229	TGTGTGGAATGGCGA[C/T]GACAGCCAGGACCTC	220441
rs766088809	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61850605	TGATTAGAGCACAAT[A/G]AATATTTACTAAGGG	220441
rs766116090	snp	A/G			downstream-variant-500B	RNF152	GRCh38.p7	18:61807996	TTAGAATAACTGATG[A/G]TGAAAATCTCAGCCA	220441
rs766169047	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61814180	ACATTAATTCCATCA[A/C]TTTTATATGCATATT	220441
rs766171322	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61867326	GTATGGTGGCATGCT[C/T]CTGTAGTCTCAGCTA	220441
rs766186675	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820815	GCAGAGTGGGAAGAC[C/T]GGAGGTTTGGGACTC	220441
rs766242016	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61840363	GTAGGCAAGCCTCAA[C/T]ATCTGTAAAATCTCC	220441
rs766242800	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825526	ACATCACAACTGACC[C/T]TGTCAGCATCATACA	220441
rs766272359	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61876440	CAATGAAGTTGAGAA[A/C]GTACACTCAGCCCAC	220441
rs766368488	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61851195	CAGGCTGTACTCACC[C/G]CATCCCTCCCTCCCA	220441
rs766376491	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813714	CTCACAAAATTAATC[C/T]GAATATGGCATAGCT	220441
rs766391552	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61888576	CATTGTAGGCTAATG[A/C]GCATTTCTGGGCACA	220441
rs766458071	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831463	TATTCAATAACGCCA[A/G]GATGAAAATGCTTCC	220441
rs766461846	in-del	-/TTTTTT			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61896218	GGGCAGGAAGGAGAA[-/TTTTTT]TTTTTTTTTTTTTTT	220441
rs766547911	snp	C/T			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868166	GAACAAGTTACCCAC[C/T]GTAGAGGTTGGCCTT	220441
rs766547996	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61856897	AAAAAGCCATAATTA[C/T]CACAATAGTGTCACC	220441
rs766567625	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61819728	GGAAGATATTAAAGA[A/G]TCAAAGAGAAGGTCA	220441
rs766593892	in-del	-/ACCAAAAAAAAAA			intron-variant	RNF152	GRCh38.p7	18:61820329	GAGAGACTCCGTCTC[-/ACCAAAAAAAAAA]AAAAAAAAAAAAAAA	220441
rs766631403	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61889275	TCCTTATTTGGAGAG[C/G]TATCTTTATAAAAAT	220441
rs766655605	snp	C/G	1.64882e-05	0.00287121	missense	RNF152	GRCh38.p7	18:61816040	GAGCCCCACCTTGCA[C/G]AGGCTGCTGTTCAGC	220441
rs766666716	snp	C/T	1.64993e-05	0.00287218	missense	RNF152	GRCh38.p7	18:61816297	GGCAGCTTGGTGACA[C/T]CGCGGCACCAGGGGC	220441
rs766684568	snp	C/T			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868202	GTTGCTGTAGACTTA[C/T]AGCATATATCTGTGT	220441
rs766845516	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836973	CAGCTCACAGATTGC[C/T]TACTAAATGATAAAG	220441
rs766856604	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811630	ACTTCAAGGGCAAAC[A/T]AAACCAGTCTGAACA	220441
rs766888593	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880017	TTAGTAGTGTATTCC[A/G]AAAAATCCTAAGCTC	220441
rs766893808	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828090	CCAGTTTTGACAAAT[A/G]TACTCACCTGTGTAA	220441
rs766914922	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847823	CACACCTACTCTTCC[C/T]TCTGCTTGGAATCTC	220441
rs766947655	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61862980	CTTGTGTGCTGATGA[C/T]TGTTGTGGTGTGAGA	220441
rs766958214	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877669	TAACAAATATTATCA[C/T]CATCTCATTTTCTGA	220441
rs767029042	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61874254	AGCGCATGAACTGAC[A/C]AAAGAGAAGAATCCA	220441
rs767050829	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815519	GTCACATTGTACGCA[A/C]TTGTACAGTTTAACG	220441
rs767071689	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888734	CCAACTTTATCCCAA[C/T]TGTGATTTCAATCAT	220441
rs767109657	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879338	AAGTAATCTAGTGAC[A/G]ATTTAAAGTATACAC	220441
rs767199942	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61861552	CTGTCATCAAGTGAG[A/G]CATGACTGTACATGT	220441
rs767224029	in-del	-/TCT			intron-variant	RNF152	GRCh38.p7	18:61869125	TAAGTTCACCATGTC[-/TCT]TCTCTAAGTAGGATG	220441
rs767225805	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61855011	TGTGGAAGAATTCAA[A/G]CAACCTAAATATTAT	220441
rs767299044	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61878855	TAATACCATCATCTT[-/G]GGGTTTAAATTCCAA	220441
rs767311997	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61841630	GGCTCACAAACCCCT[C/G]TACCTCTGAGTGGGT	220441
rs767315357	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61842219	ATTTGTCGTGAACAA[A/G]CCATTGTTCCATTTT	220441
rs767322393	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61889701	AAAGGGTGACCCAAG[G/T]TTACCCTAAACACAT	220441
rs767394914	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61831535	TCAACTTTCTAAGGA[C/G]CCAGGAACTGAAATG	220441
rs767426822	snp	A/G	8.39934e-05	0.00647994	missense	RNF152	GRCh38.p7	18:61816400	ACTTGGGCCTGCGCC[A/G]GGGGCTGTAGTAATT	220441
rs767443011	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61844119	AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA	220441
rs767459387	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837046	TAGCACCCTCAATAA[C/T]GGAAGAGCTGACATC	220441
rs767482665	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61821298	TTCCAACTCTATCCA[A/G]GTAAGTTCTAGGCCT	220441
rs767530314	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878567	CTTAGTCTGTTTGTG[C/T]TGCTACAACAAAATA	220441
rs767566216	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61848026	ACCTTATGTAATCTA[C/T]CCATCTGATTTTACT	220441
rs767586726	snp	C/G	1.86614e-05	0.00305456	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816507	CAAGGTGAAGGGGAA[C/G]GAGCTGCTTCTCAGA	220441
rs767630522	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61885915	GTGGTCTGGTAGGCT[A/G]TAAAGTCCTAAAGCT	220441
rs767661353	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811761	TTCCTGTAACATTTA[C/G]TTTTTGGCCACAAGA	220441
rs767682182	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61884273	GTGCACTCAGGTCAC[A/G]TGGCAGACGTGAAAT	220441
rs767689899	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837581	TTTTTTTAATTACTA[C/T]GGACTTATCTGCATC	220441
rs767690534	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847299	TTGAGAAATGTGCTA[C/T]TTCTATTTGCATGGG	220441
rs767720230	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810650	CAAAACTCCATCTCA[C/T]AAATAAATAAATAAA	220441
rs767767596	snp	A/G	3.30011e-05	0.00406195	missense	RNF152	GRCh38.p7	18:61816159	GAGATGGGCAGGGGC[A/G]GCATGTAGCACCCAT	220441
rs767791114	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822397	TGTGCTTTTGAAAGT[C/T]CTTTACAATAACAAT	220441
rs767833674	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61843939	GTATACTTAAAAATG[A/G]TAGAAATGCTCAATT	220441
rs767893541	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61881207	GTGATCCACCGCACC[C/T]GGCCTTCTCTCTCTC	220441
rs767929611	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61829114	AGTAAGTCAAATACC[A/C]CTGCAATAGAGTTGT	220441
rs767981047	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61890567	AGCTATGGAGACTTG[A/G]AGGTATTTGTTACTG	220441
rs767996767	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61828265	TTCTTTTTTAAGAGA[C/T]GGGGTCTTGCTATGT	220441
rs768029157	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818337	CTGAGGTGGGAGGAC[C/T]ACCTGAGCCTGGGAG	220441
rs768043776	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61860347	AGAAGCAGCACCAAA[C/T]AGCAAAGAGAAAATG	220441
rs768099717	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61817419	CACAGGTTTGAACCA[A/C]ATGGATCCACTTAAG	220441
rs768106359	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847637	GTGATACGATTTGAA[A/G]CTGAAAACTACTAAA	220441
rs768148776	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61874790	CCCAGTCTGGTTCTT[A/G]GCTATTGTGTTTTCA	220441
rs768159782	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61817559	CCGAGGGCCATCTTT[A/T]CATATTCTTGGGTTT	220441
rs768218436	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61865383	TTCATAATGTTTAAT[C/T]CATTAATAACTACAG	220441
rs768220469	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854607	TTAGTCATCTTTTGA[A/G]CGAGGTATTATTTAA	220441
rs768230032	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891496	TATTATCCCATCACA[C/T]GTTTTTTCTTCTTGC	220441
rs768297669	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808753	CCAACAGTACTGACA[C/T]ACTCAAGTCAGGATA	220441
rs768333491	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61828818	ATCTGAAGAGAAAAA[C/G]ATAGGGCCCTCTCCT	220441
rs768368105	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837460	TATTTACTGGAAGTA[C/T]TCCAGGGTAAAACGT	220441
rs768441978	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61838157	ATTACTTTTTCACTC[A/G]CCATTCTCACCCCCA	220441
rs768493974	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818922	CTTAGACAATTGTAA[C/T]GTAAATACAAGGTAC	220441
rs768498630	snp	C/T	1.64852e-05	0.00287094	synonymous-codon	RNF152	GRCh38.p7	18:61816029	CGCCTCCTGGGGAGC[C/T]CCACCTTGCAGAGGC	220441
rs768505848	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844708	AGAATAAGTGTAACC[A/G]TAGCACGGGTCGGTA	220441
rs768512536	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61892325	AATGAAGGAACAGAA[G/T]AAAGACAGTATTTCA	220441
rs768521725	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61855293	CTTAAAAGTTTAATA[A/T]AATCAGGAAGTTCTG	220441
rs768553870	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61881806	TCTACAAATAAGATG[A/C]AATAAATTTGGGGTG	220441
rs768579400	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61843467	ATTTACCCTAAAAAA[C/T]TGAAAGCAGGGTCTT	220441
rs768580299	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871506	ATGAGTAATTTACTT[A/G]GGATCACAGGGCTGA	220441
rs768584052	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861867	CCCACAGAACATTCA[C/T]CTACTCAAGTGGGAT	220441
rs768634693	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61818092	CACTCCCCCATCATG[A/T]TATATAATGTGTTAA	220441
rs768634782	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61877209	GACTTACGTATTTTG[C/G]TCAGGGGTTCTGCGT	220441
rs768728944	snp	A/G/T	3.30062e-05	0.00406229	synonymous-codon, missense	RNF152	GRCh38.p7	18:61816316	GGCACCAGGGGCACC[A/G/T]CACATCCTTCTGGCT	220441
rs768781328	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61839970	CCAGATTCAGCCATT[A/T]CTCCAGGGAGCCCTG	220441
rs768875940	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860992	TATTTTGGTACAGTT[A/G]TATAATATTTGTGAT	220441
rs768986993	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824299	TCCCCTGACAAATGA[A/G]GACTCTGGATTAGAT	220441
rs769007182	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61866748	CATTGGTGGTGACAC[C/T]GGGGGTGTGACCTCA	220441
rs769059100	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61832087	TTCATAACATCAAAT[C/G]TATTCAGTTTTAGGG	220441
rs769101655	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831711	AAACAAAAACCACTG[A/T]AAATACAATTTCTAT	220441
rs769121752	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61856402	CACAGCGCCTACTTC[C/T]TTCATGGCAGCTCTA	220441
rs769127648	snp	C/T	1.64833e-05	0.00287078	missense	RNF152	GRCh38.p7	18:61816016	GCTCCTCCTCCACCG[C/T]CTCCTGGGGAGCCCC	220441
rs769170058	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61877860	CAGGGAAAGTCAGAC[A/C]GTAGACTGCCAAAAT	220441
rs769211883	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61857247	TTGCAGATGAGAAAA[C/T]TGAGACTTAAGGAAA	220441
rs769246271	in-del	-/CT			intron-variant	RNF152	GRCh38.p7	18:61847429	CAAACAGTGGCAAAA[-/CT]CTCTCAACTCAGAAA	220441
rs769266842	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61839549	GTGGTTGTGTTGTAG[C/T]AACTTTGATCACCTG	220441
rs769313795	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61886421	GAACTGAGATCTCTT[C/T]GAGTGCCTATACAAC	220441
rs769346762	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812332	CATCATCACAGAAAG[C/T]CCTATTGAACAGTGC	220441
rs769349339	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61844793	ACTTGATTTATCAAG[G/T]GAAGGTGCAAAATGC	220441
rs769359464	snp	C/T	3.30251e-05	0.00406343	missense	RNF152	GRCh38.p7	18:61816094	ACTTCTGCTGGCTCC[C/T]GGGCAGCAGGCGGCA	220441
rs769510200	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61829011	ATGTCAAGGGTGAGG[A/T]CTCAGCAGACACAAA	220441
rs769581724	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882787	TTCCCAACCCCCACT[C/T]GGTATTACAGACTCA	220441
rs769648918	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61845493	GGAGAACATCAATCT[C/T]TCTCCTAGTTAGGTG	220441
rs769664952	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61834487	GCACCTACACACACA[C/T]CCAGCATCTAGCCAA	220441
rs769720335	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820287	TGAGCAGAGATCGCA[C/T]CACTGCACTCCAGCC	220441
rs769728971	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61871602	ATCATTAAGAAATGA[C/T]TCTCTAATGGTAAAA	220441
rs769758682	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61835206	TCCACAGTACAAAAT[A/G]GCATATTTACAAGGT	220441
rs769765920	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808952	TCATGAGCTGAGCAC[A/G]TTACCCCACATGTCT	220441
rs769798435	snp	C/G	1.6476e-05	0.00287014	missense	RNF152	GRCh38.p7	18:61815950	AAGCCACCAAGATGA[C/G]AGTGCACACCCCCGA	220441
rs769805934	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61878672	GGCACCAGTGGATTC[-/A]GTGTCTAGTGAGAGG	220441
rs769865918	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61867984	AACAATATATTAAAT[A/C]AATTTTGCTCACCTT	220441
rs770066982	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61877362	TGGACTAAGCATATA[-/AG]AGTCCATTTCAAAGA	220441
rs770071900	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61885817	GCCTTTAATTATAAA[C/T]GCAGGTGGGGCAGTC	220441
rs770097881	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811561	CATTTTAGTTTGGCA[C/T]CTGAAAAATGATGCC	220441
rs770099020	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61889472	TGCAAGCCACCAACT[A/G]CTGAATCCAGAGCAC	220441
rs770105184	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61832919	CTATAGCTCTTGTTA[C/G]TTAGTCTGTTCCCAT	220441
rs770149622	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61857611	GACCACATCTTCCAT[C/T]TCATCGCCATGTTCT	220441
rs770164283	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61858981	TCCATGTTTCTTACG[C/T]GCCGGGTGATGTCAA	220441
rs770166272	in-del	-/TTTTTTTT			intron-variant	RNF152	GRCh38.p7	18:61885988	TTCTTTTGCTTTCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT	220441
rs770167153	snp	C/T	1.64939e-05	0.0028717	missense	RNF152	GRCh38.p7	18:61816208	AGACCGGGGTGTGTT[C/T]GGAAGTGTGTGGAAT	220441
rs770186930	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884108	TGCTGGATATAAGGA[C/T]GTTAGCAACAGCTGC	220441
rs770190094	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823112	TCCAGGACACAACTG[C/T]TGCATACATGCGTAG	220441
rs770192536	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832251	AAGCATTTCAGATGT[A/G]CACAAGTAGGAAAGT	220441
rs770250314	snp	A/C/G			intron-variant	RNF152	GRCh38.p7	18:61847775	AAACCTGCTCTACCC[A/C/G]CAGTCTTCCCCTTCA	220441
rs770252689	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847054	GTATCCAGCCCAGTA[A/G]TGCACATAGTAGCTG	220441
rs770293977	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61821949	CTTCCACAAAACCCA[C/T]CCCTGGTGCCAAAAA	220441
rs770402857	snp	A/G	1.64757e-05	0.00287012	synonymous-codon	RNF152	GRCh38.p7	18:61815921	CACGATGCCGAGGAG[A/G]AAGACCAAGACGCAA	220441
rs770445804	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61856223	TGAGTAAAGCGATGA[A/C]AATGAAGCCAATGTC	220441
rs770459285	in-del	-/AC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810164	ATGCAGCCCATAGCA[-/AC]AGTTAAGAAATTAGC	220441
rs770492988	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820550	TGCGGGGAAGGATTG[C/T]TCACGTTGAGCTACG	220441
rs770535779	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61841920	GCTCAACTCTACCAC[G/T]GTAACAGAAAGCAGC	220441
rs770611181	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61881970	GGTGTATGAACAATT[A/C]ATTTTTAATAGATCT	220441
rs770612897	snp	A/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61895257	ATTTCTCTGCAGCAT[A/G]AAAACCTAAAACTCT	220441
rs770693004	in-del	-/TCTCACACAC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813276	CTCTCTCTCTCTCTC[-/TCTCACACAC]ACACACACACACACA	220441
rs770746622	in-del	-/AGA			intron-variant	RNF152	GRCh38.p7	18:61819735	ATTAAAGAGTCAAAG[-/AGA]AGGTCAGGCACAGTG	220441
rs770762206	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61827667	GCACAGAGTGTTTAT[G/T]GCTGCAGTTTCTCTA	220441
rs770773529	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61890311	CACAAGAAATATTGA[A/G]TTGTGATTAAATAGG	220441
rs770788573	snp	C/G	0.000132013	0.00812337	missense	RNF152	GRCh38.p7	18:61816260	CGGGTCGTCCGGGAG[C/G]TGCGACACGGAGAAG	220441
rs770811704	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61881062	GGGATTACAGGCGCA[A/T]GCCACCACGCCCAAC	220441
rs770841143	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836279	GGAGCCAGCTCACAG[C/T]GGAGTGGCCAAATTT	220441
rs770851079	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61862289	ATGACAATGTGTGTG[G/T]CAGAGGAGGCGGCAA	220441
rs770859651	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825437	AGCTGGCCCACTGTT[C/T]TTTCCACTCCAGAGA	220441
rs770885084	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61826451	TTGTCTTTCCTAAAG[A/G]TACCTATTTGTTCTT	220441
rs770891313	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61856846	CCAGGAAAAAAGCGA[C/T]AGGAAAATTGAGGAC	220441
rs771062676	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859114	CTACAAGTCATCACC[A/G]CCATTCAGATGCCAC	220441
rs771064809	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869844	CCTCAGCTTTTATGC[A/G]TCCATGAACTTGGCA	220441
rs771080114	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61822252	GGCTCCCAAGATAGA[A/C]CTTATTTCAAACATA	220441
rs771145555	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61879513	TTCCATCACTATGCT[A/G]TGTTTTGCGGGAGGG	220441
rs771202759	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61832492	TTTCCCAAATAGCTA[A/C]GCATACCCTGTAGAA	220441
rs771229653	in-del	-/ATAG			intron-variant	RNF152	GRCh38.p7	18:61844114	AAGAAAGAAAGAAAG[-/ATAG]AAAGAAAGAAAGAAA	220441
rs771230396	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61851479	CTCAGGAACTGTGCC[-/CA]GTTTTCTCCGTGCCT	220441
rs771232403	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813422	AAGACTCACAAAAAA[A/T]ATCTGATTTTGGTTG	220441
rs771298942	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61849002	GCCCAGGGGAGAACA[C/G]GGAAGGGGAGCCTGG	220441
rs771305576	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893134	CCGCAGTCTCCCCCG[C/T]CCACGAGTTCCCCTC	220441
rs771341137	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61847791	CAGTCTTCCCCTTCA[G/T]TCAATGGCCTGGCCT	220441
rs771367500	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61859867	CTGGACAACAGAGAC[A/T]CCACCTCAAAGAAAA	220441
rs771388869	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61838378	AGCAATCACAAAAGA[C/T]TCCAGAGATCAGCCC	220441
rs771409882	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61887374	CTAAGATGCGGCAGT[A/G]GCAACTGTCACTAAG	220441
rs771425913	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875873	CCATGGTCTCCCCAC[C/T]TTCGTCCCTTCCTGC	220441
rs771432487	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812665	TTCTTATAGTTTACT[A/C]TTTATACAACACTCA	220441
rs771521095	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61826682	TTACAAAAACAGGCT[A/G]TTATTTGTTGACCTC	220441
rs771573707	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844493	TATGTCGATCTGGTG[A/G]AAAAAGCCACACTGG	220441
rs771577976	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61874682	TATAAAGCACCGCCA[A/G]GTAGTTTTAAGCTGT	220441
rs771660256	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61884005	ATGCCATCACCTCCT[G/T]GGCTAGCTTAAGGGC	220441
rs771711019	snp	C/T	4.95389e-05	0.00497664	missense	RNF152	GRCh38.p7	18:61816121	GGCAGCCCATGTCTC[C/T]GGGCAGCAGCGCACG	220441
rs771792187	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61846950	GCAAGTTAACCTTAC[C/T]GAGTATCTGCTTCTT	220441
rs771881729	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61847584	TGTAAACATTTATTT[G/T]TCTTAAAACACACCT	220441
rs771939253	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61881712	TATTTTTCAATCTTC[A/C]TTGCAAACTAGATTT	220441
rs771952065	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864474	TGACCTCTTGGGAGG[C/T]GTCACCCTCCCCCAG	220441
rs771954381	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61861522	ACCCAAAGATGCATT[-/C]CTAAAAATATATCCC	220441
rs771973482	snp	A/G	4.94792e-05	0.00497365	missense	RNF152	GRCh38.p7	18:61816201	TTGATGAAGACCGGG[A/G]TGTGTTCGGAAGTGT	220441
rs771981090	snp	C/T			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893509	GGGGACCGCCGCTTC[C/T]CGAGCAGCGCCCCAC	220441
rs771988282	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891192	CAGAGATCAGCCTAA[C/T]AGCCTCTAGGGATCC	220441
rs771997808	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61853496	GGGGTTTCACCATGT[C/T]GGCCAGACTGGTCTT	220441
rs772003672	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836268	AAAAGGCCCCAGGAG[C/T]CAGCTCACAGTGGAG	220441
rs772043827	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61834741	ATTCAGAAATCATGA[A/G]TATAGTAAGATTCAT	220441
rs772131466	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61883735	TCATTTCACTTGGGA[A/G]GAGTGAGGCCACAGG	220441
rs772134825	snp	A/G	1.65086e-05	0.00287298	synonymous-codon	RNF152	GRCh38.p7	18:61816332	CACATCCTTCTGGCT[A/G]GTCCTCATCTGCTGC	220441
rs772152350	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818513	AACTAGTAACAATGA[A/G]AAGATCAACATACTT	220441
rs772271644	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61844487	ATCCATTATGTCGAT[A/C]TGGTGGAAAAAGCCA	220441
rs772341971	in-del	-/CACACAC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813303	ACACACACACACACA[-/CACACAC]ACACACATACACAAG	220441
rs772362218	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61833445	TGCTACAGCTGCAAA[A/T]CCAATTCCAGCTTCT	220441
rs772376336	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61863751	GGGGGCATTACACAC[-/T]TAATGTCCGAGGACA	220441
rs772450692	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813731	AATATGGCATAGCTT[A/C]AAATTGCAAGGGCAA	220441
rs772453206	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61823304	TGTCGTTTAAACATG[C/T]TTTTTGTTTTTTTGA	220441
rs772454992	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61834243	CTGTCCTTTTGGTCT[A/G]GAACCAAAAAAGAGA	220441
rs772471803	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877020	GTATGGTGAAACTCA[A/G]TTGGGGTGGCTCTTT	220441
rs772487156	snp	C/T	8.25266e-05	0.00642312	missense	RNF152	GRCh38.p7	18:61816277	GCGACACGGAGAAGC[C/T]GGGAGGCAGCTTGGT	220441
rs772510916	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61850499	GTTAAAAATAACACA[A/T]CACTATTATGATCAC	220441
rs772524857	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830238	TGGTATTTGGCCAGG[C/T]TGGTCTTGAACTCCT	220441
rs772553023	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61865795	ATATTCCCATGACAG[A/C]TGTCCCAATCCCCAA	220441
rs772571356	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866593	CCTCATCCAACCTAT[A/G]CCCTCCATCTGCCCT	220441
rs772596764	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886691	TGGGAAATGTGGCTT[A/G]ATGACAAGACATCCT	220441
rs772612857	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61831780	ACATGTTAATTACTT[-/C]CTATTTTAAAAAGTG	220441
rs772649569	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814805	GCAAGACTCCAAAAC[C/T]AGGAGAAAAGACACT	220441
rs772690284	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831671	CTGTCACTAGCTACC[A/C]TCAAAGCAGAACAAA	220441
rs772746862	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61876111	CTGGAAGACAGGAGC[C/G]ACTTACCCCCATGCT	220441
rs772747542	snp	A/C			downstream-variant-500B	RNF152	GRCh38.p7	18:61807873	TGGGCTTACTCATTA[A/C]AGATGTGTTCTTTGG	220441
rs772789598	in-del	-/AA/ACAG			intron-variant	RNF152	GRCh38.p7	18:61844110	AAGAAAGAAAGAAAG[-/AA/ACAG]AAAGAAAGAAAGAAA	220441
rs772858665	snp	C/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892770	CCAGAGACACCCAGG[C/G]GCTACCCAGATCGTG	220441
rs772869956	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61830188	CACTGTAGTCTGGCT[A/G]ATTTTTTGTATATTT	220441
rs772873208	snp	C/T	1.64936e-05	0.00287168	missense	RNF152	GRCh38.p7	18:61816204	ATGAAGACCGGGGTG[C/T]GTTCGGAAGTGTGTG	220441
rs772915062	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808973	CCACATGTCTTCAAC[C/T]GAAGCATCCTGAATT	220441
rs772926261	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61881173	CCCACCTCAGCCTCC[A/C]AAAGTGCTGGGATTA	220441
rs772960354	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837142	TCGTCTTGCATCCAG[C/T]CAGTCATGACAGGGA	220441
rs772977100	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824396	GTTTCCAACCGCATG[A/G]CAGTACTGCCAGGCC	220441
rs773015159	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61838724	ACAAAGATTGATGCA[C/T]CTCCCTCTGCTGTTC	220441
rs773024315	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61888470	CTATACGACCAATCT[A/G]TTTTTCACTTTCAAT	220441
rs773052914	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61825465	AGATACTGGAGAGAG[A/C]AGAAAACTCAGGGGA	220441
rs773071334	snp	C/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815175	GTTTATTGCTCCCCT[C/G]TTGAGCTTTCAGTTC	220441
rs773265670	snp	A/G	1.64944e-05	0.00287175	synonymous-codon	RNF152	GRCh38.p7	18:61816224	GGAAGTGTGTGGAAT[A/G]GCGATGACAGCCAGG	220441
rs773286238	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889523	GCATCCAACTCTTTT[C/T]AGGGAGAGTGAGGCA	220441
rs773296819	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61820946	AGGGATGATGGAGTT[A/G]TGGCTGAAGGTCAAG	220441
rs773333059	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813342	TGCACACCCCAACAA[A/T]CAGGTACACAAATAA	220441
rs773358286	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61832315	TGTTTTTGTTTTAAG[C/T]GCACATGTATATATG	220441
rs773372359	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61857629	ATCGCCATGTTCTGA[C/T]GATACAGGGACACAA	220441
rs773401074	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831726	TAAATACAATTTCTA[A/T]GTCAGATAGAAAGCA	220441
rs773544811	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811601	CCACACCAAATACAA[C/T]GACAAGCTGGCCAAC	220441
rs773622407	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812539	TGCCCCAAGTCATTA[C/T]ACAAAATTTTTCCAA	220441
rs773658728	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61841921	TCAACTCTACCACTG[-/T]TAACAGAAAGCAGCC	220441
rs773700574	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836922	TCATTGGATTACAGG[C/T]TTTGACAGACAGGAT	220441
rs773802366	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872549	TCATGAAATCATGCC[C/T]CTCTCCCAACCCCCA	220441
rs773816160	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61847061	GCCCAGTAGTGCACA[C/T]AGTAGCTGCTCAGCA	220441
rs773851519	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825586	TGCAAGATATTAAGA[C/T]GGTAACTTAAGGTCT	220441
rs773855968	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61884114	ATATAAGGACGTTAG[A/C]AACAGCTGCCATTTA	220441
rs773895953	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61835358	GAAGTTTATGAATGG[C/T]TTTGGAATAGGAGCC	220441
rs773946567	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825733	GGAGAGCAAAGGTCT[C/T]TCTCTGCTATAGCCC	220441
rs773968202	snp	C/G	7.40069e-05	0.0060826	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816495	GAAGGGCAAGGCCAA[C/G]GTGAAGGGGAAGGAG	220441
rs773971718	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61881990	TTAATAGATCTGACA[C/T]CTCTGTTGGAAAAAA	220441
rs773980348	snp	A/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810224	ATTGGAAAACATGAC[A/T]AATAACAGTTTTTTA	220441
rs774013240	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61820560	GATTGCTCACGTTGA[A/G]CTACGGGTGGGTAGG	220441
rs774060668	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879135	GGATTCAACCAACCA[C/T]GGATCAAAAATATTC	220441
rs774070748	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61822884	CATCTTTCTGATACA[A/G]GCCATCTACTTAAAT	220441
rs774105316	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61845961	GCCCTCCTGAGTGGG[G/T]TTAGTGCCCCTTATA	220441
rs774112342	snp	C/T	1.64868e-05	0.00287109	missense	RNF152	GRCh38.p7	18:61816033	TCCTGGGGAGCCCCA[C/T]CTTGCAGAGGCTGCT	220441
rs774116117	snp	A/G	1.65132e-05	0.00287339	missense	RNF152	GRCh38.p7	18:61816106	TCCCGGGCAGCAGGC[A/G]GCAGCCCATGTCTCC	220441
rs774126340	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61862360	CAGTTGGATCAGGGA[C/G]TGCCCAGAGAGGAGA	220441
rs774146039	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878316	CCACACTGCACAGGA[C/T]GGTCTTCCCACAATA	220441
rs774187166	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61877385	TTTCAAAGACTGTCA[C/T]ATTATACAGTGATTT	220441
rs774216258	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61852470	CATCGCTCATACACT[G/T]ATCTGTGTATATCAT	220441
rs774223869	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815357	TAAAAGCCTTAGCAA[C/T]TAAATGAAGACTGGG	220441
rs774240329	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61890343	TCATATGCCCAGTTC[G/T]GGCCAAAGTGATGGA	220441
rs774304290	in-del	-/CTCACACACA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813277	TCTCTCTCTCTCTCT[-/CTCACACACA]CACACACACACACAC	220441
rs774308142	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811671	TGCTTGCTCTTATAT[C/T]TGCACCTTACTAATA	220441
rs774399172	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61821634	GTGATTACTTTAGAG[-/C]AAGGGTCTCCAACCC	220441
rs774436512	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61889617	CCTAAACTCTCTGGG[A/T]GTTCTACTAGTCCTG	220441
rs774443175	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61845321	AAGAGCAATGCTAGG[A/G]ATCTCAAATAAAACC	220441
rs774483267	in-del	-/TTTTTTTTTT			intron-variant	RNF152	GRCh38.p7	18:61885986	CTTTCTTTTGCTTTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	220441
rs774493190	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869280	GGTCAAAAGCTGTCA[A/G]GGGTCTTCTTCCAAT	220441
rs774508796	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847962	TCTCACCACACTCAC[A/G]CTTCCCTTCGTGTGA	220441
rs774521488	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61864760	GTATGGTTGAAAGGA[G/T]TTTATGGTCGGGCAC	220441
rs774567109	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61833406	TCAAAGAATCCAAAT[G/T]TCAGGTGATTCACAA	220441
rs774578850	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61838406	CCCTGTAACCAGAGA[C/T]GGAGGAGTCATACTT	220441
rs774605567	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854686	GATGGTCATACTGCT[A/G]TTGGTAACCTGGAAT	220441
rs774606346	in-del	-/GGAAGGAAG			intron-variant	RNF152	GRCh38.p7	18:61844185	GGAGGAAGAGAGGAA[-/GGAAGGAAG]GGAAGGAGGGAGGGA	220441
rs774608293	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61891720	CTATGTTTTTAAAGT[C/T]ACCTTCCAAAACAAA	220441
rs774610682	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61857970	AGGTAGTGGGGATGG[C/G]TTTAGCTTTACGTTT	220441
rs774776071	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844117	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs774798163	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875900	CTGCCCCAATCCATA[C/T]TGATGACTGCCAGAT	220441
rs774807618	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61865556	CCCATTGCCTTTATA[C/G]ACTTTGTTGAATTGT	220441
rs774840138	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847795	CTTCCCCTTCAGTCA[A/G]TGGCCTGGCCTTCAC	220441
rs774877088	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812751	TAAAAATTCAAACCA[C/T]ATGGTTTGATAGTTG	220441
rs774890612	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61849046	GCATTCCTACTTTCC[C/G]GTCATTGTCAGCTGT	220441
rs774893254	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828596	CACTGGCAAATTTAT[A/G]TATTTAAAACCCAAT	220441
rs774907864	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61831921	ATAGTATTATGTGTG[-/T]TGGGGGGGTGTGGGT	220441
rs774976787	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837542	TCTCTCCACATTTCT[A/G]TGTATTTTACATTTT	220441
rs774996944	snp	A/G	3.6491e-05	0.00427132	utr-variant-5-prime	RNF152	GRCh38.p7	18:61816481	TGGACCGTGAGCAGG[A/G]AGGGCAAGGCCAAGG	220441
rs775103128	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61872830	TTATTACTAAAGTAC[A/T]CCATGACTGAAATTA	220441
rs775137278	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61837410	GGTGTGATAATGGTG[C/T]GATTATGTAAGAGAA	220441
rs775142644	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61811312	AATCTGGTCTTTATA[A/G]GAAATATATCTCAAA	220441
rs775183539	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61884049	ACCATGCCTATTCAT[C/T]CCGATATTTCCAGAA	220441
rs775183625	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61825955	ATTATATTTTATCTA[C/T]GTCAGGGACCCACAA	220441
rs775212900	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61889759	GCCCTGTGGTCTCTG[-/C]TGCAGGAGGCCACCT	220441
rs775216150	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61857213	TGTAACAGGGAGAAA[A/G]TGCAGACACTTTTCT	220441
rs775253699	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61817367	GGCTTGTACCAAGTA[A/G]CACAACTAAAAGCAA	220441
rs775299103	in-del	-/CACACACAC			cds-indel	RNF152	GRCh38.p7	18:61813299	ACACACACACACACA[-/CACACACAC]ACACACACATACACA	220441
rs775308635	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61869368	AGGATACATAAAAAC[A/G]ACCCCTACTTCCAAA	220441
rs775351731	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61843372	TCTATAGCAATAACT[A/G]TTGTTTTAAAACAGT	220441
rs775357089	snp	A/G	1.64762e-05	0.00287016	missense	RNF152	GRCh38.p7	18:61815952	GCCACCAAGATGACA[A/G]TGCACACCCCCGACC	220441
rs775374924	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880696	TCTGATAAATTTCCA[C/T]GTCATTTTGTAAAAC	220441
rs775397317	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812815	CCTCCTTTCATTTTC[C/T]CAGAGAGGTAGATGC	220441
rs775408371	snp	C/G/T	3.29686e-05	0.00405998	missense	RNF152	GRCh38.p7	18:61816019	CCTCCTCCACCGCCT[C/G/T]CTGGGGAGCCCCACC	220441
rs775428419	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61833449	ACAGCTGCAAATCCA[A/G]TTCCAGCTTCTACCA	220441
rs775544486	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61870031	GAAGGAAAAGACAGG[A/C]AAGTCACCATATAAC	220441
rs775547932	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61854450	ACAATAGGTAACACC[A/G]GTGTCTTCCATGTTC	220441
rs775569727	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61850560	GATAAATTTCAAGTT[A/T]CTGAGAGGCAGACTC	220441
rs775571462	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61879588	CTACACAAAGGAATG[C/G]GAATACAAAAGGGTA	220441
rs775571714	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61838557	CCCTTTTCTAGAATG[A/C]ACAGTCTTCATTCCT	220441
rs775729166	in-del	-/CACACACACAC			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813299	ACACACACACACACA[-/CACACACACAC]ACACACATACACAAG	220441
rs775730144	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61819319	CCAGAGACTGTGGAC[C/T]GTGGGCAGCCCCCAG	220441
rs775754174	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859312	AACAGGCAACAGAGC[A/G]TGAGAGGGCTGTTGT	220441
rs775804132	snp	A/G	4.94784e-05	0.00497361	synonymous-codon	RNF152	GRCh38.p7	18:61816209	GACCGGGGTGTGTTC[A/G]GAAGTGTGTGGAATG	220441
rs775804270	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61823366	AGTGGTGCAATCTTG[A/G]CTCACCGCAACCTCC	220441
rs775961266	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61891552	ATTGCTGACATAAAA[A/G]TTACTTGTCAAAAAT	220441
rs776017642	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61839883	TATGTCCCCATCATT[C/T]TTTGAGCACTGCCTT	220441
rs776112129	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829237	AGGCAGGAAGGAGAC[A/G]CAGGGCACAGCCTGG	220441
rs776177154	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61817456	TTTTTTGAATAGATA[C/T]GGTCAGCCCTTTCTA	220441
rs776181105	snp	C/T	4.94254e-05	0.00497094	missense	RNF152	GRCh38.p7	18:61815932	GGAGGAAGACCAAGA[C/T]GCAAGCCACCAAGAT	220441
rs776207623	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866121	AAGGGAATTTGGAGG[A/G]CTGAGTGGCACAGGG	220441
rs776254447	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828889	GAAGAAACTACAGTC[A/G]TGTGATTGATACTTC	220441
rs776312340	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61874892	TTTATTGGGTACAGA[C/T]CTTAAACACTCTTTA	220441
rs776378115	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61827987	AAATCCAGATTTCTC[C/T]TCTTGCTTTCTTAAA	220441
rs776401009	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61864734	GAGTCATCTCATTAG[C/T]ATAAGCCAAGGTATG	220441
rs776406398	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880999	GCTCACTGCAACCTC[C/T]GCCTCTGGGGTTCAA	220441
rs776427302	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61862371	GGGACTGCCCAGAGA[A/G]GAGATGACCATCCTG	220441
rs776483330	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61834428	GATCATATTTTGTGT[C/T]CTTTTAGTCTCCCAC	220441
rs776497043	snp	C/G	1.74263e-05	0.00295175	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815804	TCTCATCATCAACCT[C/G]CTCAACCCCTAAGTT	220441
rs776499762	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61824375	AATTGCTGAAAACAC[C/T]GCTGGGTTTCCAACC	220441
rs776508311	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61871543	ACAGAAGGGTTACTG[C/T]CCTCAGCCGACCAAA	220441
rs776513411	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61860283	AGCCCTAGAAAACTC[A/C]TCTAAGGGGGAAGCA	220441
rs776569090	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61840005	CTTTTAGTGAAAAAT[A/G]TCAGTTAGAAACCAA	220441
rs776589162	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61844714	AGTGTAACCATAGCA[C/T]GGGTCGGTAGGTCAT	220441
rs776596778	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861164	TTGTAAAGTCTACAG[C/T]AGTGTACAGAAATGT	220441
rs776651740	in-del	-/AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA/G			intron-variant	RNF152	GRCh38.p7	18:61844094	AAGAAAGAAAGAAAG[lengthTooLong]AAAGAAAGAAAGAAA	220441
rs776653695	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61820069	GCATGGTGGCTCACG[C/T]CTGTAATCCTAGCAC	220441
rs776680333	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61838502	ATCTCAAAGAACCAA[C/G]ATTCAATGAAATGGA	220441
rs776697398	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830354	TTTTATCATCCCAAA[C/T]AGAACTCCATACTCA	220441
rs776727553	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61877455	ATCCACATCTGTCAC[G/T]GTTCCCAAAAAATGT	220441
rs776784863	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841232	TCCCATTAAAAGTCA[C/T]TACAAAGGCCTAAAA	220441
rs776818747	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882881	TCCACCCAACCCACA[C/T]TACCATCATGCATAC	220441
rs776831287	snp	G/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61815111	ATGGCTTGAGGAAAA[G/T]CGGCATACAGGTTTT	220441
rs776841042	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61888365	CAGACGGTTCCCTAC[G/T]TACAACTGTTTGACC	220441
rs776859982	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61887023	AGAGGACATTTTAGG[C/G]CACAGAATGTGCTAG	220441
rs776899865	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61884446	AGCTTTGCCATTACA[-/AA]AAAAAAAAAAAGCAG	220441
rs776921550	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810255	CTGAATTTTAACTCC[A/G]ATTACAGCTAAATCG	220441
rs776949705	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61820837	TTGGGACTCAAAGAA[A/C]CTTGGGCTCAAAGCC	220441
rs776960598	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830915	TTGAGATTTTGTACC[C/T]AGCAAAGTCCTGACT	220441
rs777014047	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61831721	CACTGTAAATACAAT[A/T]TCTATGTCAGATAGA	220441
rs777069194	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61846215	TCTCAACCCAAACAC[A/T]CTCTCTTGTTCTTGC	220441
rs777076052	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61819374	TAGAGTGAGCAATGG[A/G]AAAACACCAGAAAGG	220441
rs777083659	in-del	-/AATCG			intron-variant	RNF152	GRCh38.p7	18:61891908	TCTTCCTACAAGAAA[-/AATCG]AAAGCCCATTTCCAT	220441
rs777084314	snp	A/T			intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868063	TCACTTAGAAAGCTG[A/T]CTGAGGAGATTCATG	220441
rs777169544	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866878	GGCAAATCATCAGTG[A/G]AACTTTAAAAAGCAA	220441
rs777188325	snp	C/G			upstream-variant-2KB, intron-variant	RNF152, LOC105372159	GRCh38.p7	18:61893323	ACACAGCGCGGCAAT[C/G]CCGAGCATCTTTCTT	220441
rs777265950	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831665	TTCCTACTGTCACTA[A/G]CTACCCTCAAAGCAG	220441
rs777326831	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61876372	TAATGAACTACTTTC[-/T]GACATGGAAGCATTA	220441
rs777336806	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61856503	AAATCCCATATAAAG[G/T]GTCATAGCTAGGACC	220441
rs777353696	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61867704	CACCATCCTGGGATA[C/T]AATTCTGACTATAAA	220441
rs777364838	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61873611	AGTGCTGGGATTACA[A/G]GCATGAGCCACCACG	220441
rs777389138	snp	A/G			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809484	GTTGAATTAAAAATG[A/G]GCCATCCCTTTGGAA	220441
rs777399254	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61831733	AATTTCTATGTCAGA[C/T]AGAAAGCAATAATTC	220441
rs777420506	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847355	CTTTCATTGCATAAT[A/G]CCATAAAACACAGCT	220441
rs777535836	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61836167	ATCTTTGGAGAAATG[A/G]TTGATTCCAGGTCTG	220441
rs777553952	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61826411	AAAACATTCTTATCT[C/G]CCGTTTGAACTCCTA	220441
rs777555922	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61837200	CTCCTCAAAACTCTC[A/C]ATGTCATGGAAAGGA	220441
rs777583010	snp	A/G	1.65018e-05	0.00287239	missense	RNF152	GRCh38.p7	18:61816301	GCTTGGTGACACCGC[A/G]GCACCAGGGGCACCG	220441
rs777630175	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61883685	GGGGGTCACTCTACT[C/T]CCAAGAAAGCAGACC	220441
rs777650437	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61866974	GGGTGGAGGGATGGG[A/G]AGGGCCTTATGTGGG	220441
rs777722574	snp	A/G	1.65034e-05	0.00287253	missense	RNF152	GRCh38.p7	18:61816255	ACCTCCGGGTCGTCC[A/G]GGAGCTGCGACACGG	220441
rs777732487	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61842916	AGGTCCCTCTGACAA[C/G]ATGTGGAAATTATGG	220441
rs777736999	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61882801	TTGGTATTACAGACT[C/T]ATCACGAAAACCCTC	220441
rs777740368	in-del	-/TATT			intron-variant	RNF152	GRCh38.p7	18:61885021	GTGGAGTGGATGGAC[-/TATT]TATCCCAGTTAAGGA	220441
rs777770586	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61879416	GGACTTGAGCATGCA[C/T]GGATCTTGGTTTCTA	220441
rs777819674	snp	A/G	5.30753e-05	0.0051512	missense	RNF152	GRCh38.p7	18:61816456	GAGTCCTGGGACAGC[A/G]TCTCCATGGTGGACC	220441
rs777860683	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869077	GAATATTCTAACATC[C/T]CAGAGGTAATCTCGA	220441
rs777862867	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61880195	AATTTCCCAACAAAA[C/T]TTGACACCCAAGCTT	220441
rs777885077	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61880966	TTACCCAGGCTGGAG[G/T]GCAGTGATGCAATCT	220441
rs777928561	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61827508	CATTAAAAAATATAT[A/T]TTTCTTTAAATTTCC	220441
rs777937786	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61827263	ACAGCAGTATCATAC[A/G]GTGGGTCACCTTGAC	220441
rs777999066	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61854075	CAACTCCAAGCCCCA[C/T]GTTCTTTCTGCCACT	220441
rs778011683	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61860548	AACCTACCATGCTGC[C/T]GGTTGCATAAGAGTC	220441
rs778081312	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61834175	CATCTCTAAAAGCAA[C/T]ATGCCTTTCTCATCT	220441
rs778193942	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61859611	AGGCCGGGCACGGTG[A/G]CTCATGCCTGCAATC	220441
rs778210335	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61848939	CCACAGGGATGCAGA[A/T]TCTCCAGCACAAACC	220441
rs778254861	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61823889	GGATGTGCCGTGGAG[A/C]CAAGGGCATCCTGTG	220441
rs778265045	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61821853	CTTTATGAGGATCTA[A/C]CTAATGCCTGATGAT	220441
rs778265960	snp	C/T	1.64825e-05	0.00287071	missense	RNF152	GRCh38.p7	18:61816009	CTGTCCTGCTCCTCC[C/T]CCACCGCCTCCTGGG	220441
rs778284148	in-del	-/CA			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814728	CTTTCAAAAAAGAAT[-/CA]CAGGCCATTTATTAA	220441
rs778287132	snp	A/G	4.95021e-05	0.0049748	missense	RNF152	GRCh38.p7	18:61816246	ACAGCCAGGACCTCC[A/G]GGTCGTCCGGGAGCT	220441
rs778299161	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61869807	CTTCATAAACTCAGA[C/T]AAGCCACTTACCCAC	220441
rs778381641	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61819648	GGATCATGAAGAGAA[A/G]TACAATGAGTTCTGT	220441
rs778386642	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61844163	GAAAAGGAAGGAAGG[A/G]AGGAAGGGAGGAAGA	220441
rs778413236	in-del	-/CTCTCACACACACA			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813275	TCTCTCTCTCTCTCT[-/CTCTCACACACACA]CACACACACACACAC	220441
rs778500116	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847576	AACCATGGTGTAAAC[A/G]TTTATTTTTCTTAAA	220441
rs778521691	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61872211	AGAACAGCACCAAAA[-/G]GATAGTGCTAAACCA	220441
rs778540931	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61837796	CTTAGTGCTGTTCTT[A/G]ATATAATTTCTATTT	220441
rs778553456	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822638	CAGATAGTTTTACTC[C/T]GCTTACACTCTTAAG	220441
rs778677527	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61848532	ACACAGCCCCCCAGG[C/T]TGTACGTGGCCTCAG	220441
rs778767287	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809856	AGGCAGTGAATCCTG[-/A]AAAAAAAAAAAAAAA	220441
rs778789720	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61885027	TGGATGGACTATTTA[A/T]CCCAGTTAAGGACAC	220441
rs778791604	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61873625	AGGCATGAGCCACCA[C/T]GCCCAGCCTCAGTCT	220441
rs778881685	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61874596	GAAGGTGGCAGTACA[C/T]AGGCTGAGTGGCAAG	220441
rs778940285	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812235	ATCCAGTTCTTCCCT[C/T]GTAGTAACCCCATTT	220441
rs779018912	snp	A/G	3.50342e-05	0.0041852	missense	RNF152	GRCh38.p7	18:61816450	AGCAGAGAGTCCTGG[A/G]ACAGCGTCTCCATGG	220441
rs779133541	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61818235	TGAGACCAGCCTGGG[A/C]AACATGGTGAAACCC	220441
rs779186934	snp	C/T	3.29533e-05	0.00405901	missense	RNF152	GRCh38.p7	18:61815908	ACATGTTGTGAAGCA[C/T]GATGCCGAGGAGGAA	220441
rs779190692	in-del	-/C			intron-variant	RNF152	GRCh38.p7	18:61819754	GGTCAGGCACAGTGG[-/C]TCACGCCTGTAATCT	220441
rs779249819	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61861659	TTTATGTAGCTCACA[C/G]TTCCACTGGCCAGAA	220441
rs779253254	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61891071	TACACCCAACCCCAA[A/C]CCCTTGAGTCCATTA	220441
rs779264227	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61851540	GGGTATCTTATTTGC[C/T]CATTTTCTACAGATG	220441
rs779312907	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61824779	GAAGCCAAGGTTAGC[A/G]CTGGCATTCATCAAA	220441
rs779406589	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61837663	TCTTTTTATTTCTAA[-/G]ATACTTGATAGAAGA	220441
rs779445900	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61860566	TTGCATAAGAGTCTA[A/G]CACACACAATCATGT	220441
rs779452187	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61876966	TATCCTCAAGCCAGA[C/T]TTGCTGTATTTCCTG	220441
rs779474807	in-del	-/ATA			intron-variant	RNF152	GRCh38.p7	18:61874043	ATCATTCTTCATACT[-/ATA]ATAAGTGTACTTTGT	220441
rs779484773	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61874752	TACTTGGGTTTAGGG[C/G]TAAGCATAGTGGGGT	220441
rs779525357	snp	A/G	3.30289e-05	0.00406366	synonymous-codon	RNF152	GRCh38.p7	18:61816095	CTTCTGCTGGCTCCC[A/G]GGCAGCAGGCGGCAG	220441
rs779555068	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61886848	TGGCCTTTGTAGAAT[A/G]AATGAATGAATGTTG	220441
rs779574242	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61864547	TTTGATGGAGGCTTC[A/G]CTGTGTAGACATGGT	220441
rs779580846	snp	A/C	4.94915e-05	0.00497426	missense	RNF152	GRCh38.p7	18:61816171	GGCAGCATGTAGCAC[A/C]CATTGCTGGGAAGTT	220441
rs779596469	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61828233	GAATTTGAGTTTGCG[-/T]TTTTTTCTTCCTTCC	220441
rs779596614	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61812297	TACCGTACCAGACGG[C/T]ACAGGTTTTCGAGCA	220441
rs779608882	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61859523	AGAGAAAAGGAGCAT[C/T]ACCCACCTGTGTGGG	220441
rs779617588	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61822952	AAAATAATCACAATT[C/T]CATTTCATCTGGTAT	220441
rs779649757	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61875703	TACCTCAGACTTGAA[C/T]ACCTGTGTATGTCTC	220441
rs779655958	snp	A/C			utr-variant-3-prime	RNF152	GRCh38.p7	18:61813009	CTTTCTGCAGAATTA[A/C]AAAACGGACTCATCT	220441
rs779697935	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61848605	CGGAAGGAACTGTAC[A/G]TAGGTCTATGCAGGG	220441
rs779714304	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61838104	AAACCCTCAGCCCTT[C/T]ATCAGTCCCTATGAA	220441
rs779725824	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61844591	AATATTTACAGTAGC[A/T]TTTTTTTTATCTAAA	220441
rs779733233	in-del	-/A			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808096	ATGAACTTTAATCAT[-/A]GCAAATGTGTTTTTA	220441
rs779760423	in-del	-/G			intron-variant	RNF152	GRCh38.p7	18:61845921	GTGGGGCTTTGTGTG[-/G]GGGGGGCGTGGTGAT	220441
rs779783201	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61818874	GTCATTGCCCATAAG[A/G]AAGTCCTGGCCTAGA	220441
rs779818259	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61855251	AGGATGTCATTGTAA[C/G]AGAATTCTGGTTTAC	220441
rs779833664	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61829958	TAGCCATTTGAAAGT[A/G]TACAATTCAGTGGCT	220441
rs779890042	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61873025	ATATTTTAATGGACT[-/A]CAACATATGAATGCT	220441
rs779892365	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61847716	GCGTCTCAAAGCTAA[A/G]ATTTCCAAAATGGAA	220441
rs779936115	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61872178	TAAACAACTAGGTCT[C/T]GTGAGAACTCTATCA	220441
rs779941491	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61892134	AGTTTTTGGAAAAGC[C/T]CCAATAACCTAAAGA	220441
rs780003043	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61828738	CATAGAGTAACAAAT[A/G]CTACTATTAATGTAG	220441
rs780088872	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61839286	AGAAAACAGGTTGCA[C/T]TTACTTGTCATAATC	220441
rs780118650	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61860770	CACAGGAAATAACAG[A/C]TCCATGCGTGTATTA	220441
rs780153234	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61835128	ATTATCTAATAAAGC[C/T]ACATATGATTTAACT	220441
rs780179925	snp	A/G	8.25008e-05	0.00642212	missense	RNF152	GRCh38.p7	18:61815878	ATATCACAGTGAAGC[A/G]CTTAGAAATGCAAGA	220441
rs780192012	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808693	TGAAAAAATATATGA[C/T]GGCAACCAGGATATA	220441
rs780214175	in-del	-/TGG	3.56316e-05	0.00422072	cds-indel	RNF152	GRCh38.p7	18:61816463	GGGACAGCGTCTCCA[-/TGG]TGGACCGTGAGCAGG	220441
rs780239788	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61819872	CTAAAAATAAAAAAA[A/T]TAGCTGGGTGTGGTG	220441
rs780239790	in-del	-/AAAAAACAAAAAAC			intron-variant	RNF152	GRCh38.p7	18:61818432	TGTCTCAAATTAAAA[-/AAAAAACAAAAAAC]AAAAAACAAGAAAAA	220441
rs780282314	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61845348	AACCTCATTAAACAA[C/T]GAAGTCCGCTCAGAG	220441
rs780288649	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61809594	CCCATGGAAATAAAT[C/T]TGGAGCAGTGTTCTA	220441
rs780316602	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61878924	AGTTCCTACAGCTAA[A/G]GAACTTACACTAGAG	220441
rs780349342	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61878304	CTACTAAACATCCCA[C/T]ACTGCACAGGACGGT	220441
rs780382771	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61852717	CAATTGTCTTGGGGG[A/T]GCTGCCTGGACATCA	220441
rs780384376	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61871343	ACTATTCTGAGAATT[A/G]GGTAACACATATACA	220441
rs780401157	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61841802	TAAATCACTAATCCT[A/G]CTTTCAGTGGCAAGG	220441
rs780402081	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61888322	TGAGTCAATTAGAAA[C/T]TGAAAATCCCTAAGC	220441
rs780425263	in-del	-/ATGTT			intron-variant	RNF152	GRCh38.p7	18:61881740	TTTGCCCCCAAGAGA[-/ATGTT]ATTTTAAGGAGCACA	220441
rs780480275	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61831117	TTTATGTTTATAGAG[A/G]TTAAACCTTAACAGC	220441
rs780634652	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61853512	GGCCAGACTGGTCTT[C/G]AACTCCTGACCTCAG	220441
rs780641160	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61826009	AGTATATCCAGCTTC[C/T]AGGCTTTGCGGATCC	220441
rs780644888	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF152	GRCh38.p7	18:61814910	GACGTGTAGGAGACC[A/G]CTCGCTGGGTCAAGA	220441
rs780682488	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852968	CCTGGTCTTCCTGAC[C/T]TATTCTAATCACAAC	220441
rs780737153	in-del	-/TTAG			intron-variant	RNF152	GRCh38.p7	18:61832413	CCTAAGCTAGTCATT[-/TTAG]TTACAGTAATTAAGT	220441
rs780848925	in-del	-/AA			intron-variant	RNF152	GRCh38.p7	18:61844093	AAAGAAAGAAAGAAA[-/AA]GAAAGAAAGAAAGAA	220441
rs780857015	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61831652	ACACAATGCTCACTT[A/C]CTACTGTCACTAGCT	220441
rs780866230	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61835181	CAAGTATTCATTCTG[A/C]AAATACAGCTCCACA	220441
rs780909887	snp	C/T	1.65048e-05	0.00287265	synonymous-codon	RNF152	GRCh38.p7	18:61816086	GGTGACGGACTTCTG[C/T]TGGCTCCCGGGCAGC	220441
rs780949366	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61838271	ATATCCTTCAGTGAA[A/T]TGAATTAATATGAAA	220441
rs781017884	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808811	ATGGTTAAGAGGATT[C/T]TAGAGTCTGTCTGCA	220441
rs781099616	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61887781	ATCTCTTCAATTCTT[G/T]TCAAACCTCAGTGAG	220441
rs781119242	snp	A/G	1.65002e-05	0.00287225	missense	RNF152	GRCh38.p7	18:61816313	CGCGGCACCAGGGGC[A/G]CCGCACATCCTTCTG	220441
rs781143365	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61855908	AATAAACTGAGTAAA[A/C]TGAAAGAGAGTACAC	220441
rs781144344	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61852854	AGGTACTAATGGCCA[C/T]GAATAATTTCACAAT	220441
rs781162468	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61872269	ATCACCTTTCACCAG[A/G]CCCCACCTCCAACAC	220441
rs781169935	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61892513	AACATTCAGATACAA[C/T]TGCCTGTGTATGAAT	220441
rs781172675	snp	A/G	0.000100896	0.00710197	synonymous-codon	RNF152	GRCh38.p7	18:61816404	GGGCCTGCGCCGGGG[A/G]CTGTAGTAATTGAAA	220441
rs781196694	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61889205	CTCCCTAGGTTGATA[C/T]TGATATCCCCTCAGT	220441
rs781232093	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61830803	TTCTCAGTGAGGCAG[C/T]TGGATGGAGGAAGCA	220441
rs781242557	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61867102	GTAGGAAGAAAGCCT[A/G]TGGCAGATTTTAAAT	220441
rs781261831	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61881868	GAAGACATTTTTCCT[G/T]GTTAATTAACAGTCT	220441
rs781277366	in-del	-/GAGAGGAAGGAAGGAAG			intron-variant	RNF152	GRCh38.p7	18:61844177	GGAGGAAGGGAGGAA[-/GAGAGGAAGGAAGGAAG]GGAAGGAGGGAGGGA	220441
rs781381189	in-del	-/C	1.64777e-05	0.00287029	frameshift-variant	RNF152	GRCh38.p7	18:61815988	GAGCTTTTCACCACG[-/C]CCCGCCTGTCCTGCT	220441
rs781406366	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61880525	TGCCTCCCAGATAAC[A/G]TGATTAAAGCACTTT	220441
rs781413440	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61863122	CCAAATGTGTTGCCC[A/G]TAAAACATTTGCTCT	220441
rs781425105	in-del	-/AT			utr-variant-3-prime	RNF152	GRCh38.p7	18:61808752	CCCAACAGTACTGAC[-/AT]ACTCAAGTCAGGATA	220441
rs781440422	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61836104	TGAGCACACTTAGTT[C/T]CTAGATCTTGGTATC	220441
rs781489685	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61855808	GAGCCCAGCAGGTAC[A/G]AGCAATACCCAGGCA	220441
rs781491196	snp	A/G			synonymous-codon	RNF152	GRCh38.p7	18:61816104	GCTCCCGGGCAGCAG[A/G]CGGCAGCCCATGTCT	220441
rs781508561	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61832089	CATAACATCAAATGT[A/G]TTCAGTTTTAGGGGA	220441
rs781509083	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61841865	AGGGACAGATGGTAA[C/T]ATTTTAGGCTTTGTG	220441
rs781595859	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61842719	CATGGCTGGGGAGGC[C/G]TCACAATCATGGTGG	220441
rs781598599	snp	C/G			intron-variant	RNF152	GRCh38.p7	18:61821909	AACCATCGGTCCCTA[C/G]CCATCCGTCCTGTGG	220441
rs781609999	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61861895	GATCTGCTCCTGTGA[C/T]CTAAACATCTCCTAT	220441
rs781644911	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61890118	AATTACAGGTTGGAA[C/T]AGTAAATATACAGGT	220441
rs781645030	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61877957	TGACACTTGGCAAGG[A/G]AGCATCTGCTCCACA	220441
rs796176137	in-del	AC/CCAAAAAAAAAAAAAAA			intron-variant	RNF152	GRCh38.p7	18:61820330	GAGACTCCGTCTCAC[AC/CCAAAAAAAAAAAAAAA]AAAAAAAAAAAAGAG	220441
rs796178270	snp	C/T			utr-variant-3-prime	RNF152	GRCh38.p7	18:61810305	TGTGTAGTAAGTCAG[C/T]TGTGTCAGAAAAATC	220441
rs796203043	snp	G/T			intron-variant	RNF152	GRCh38.p7	18:61817117	CAGTTTACATATATG[G/T]GTTAGGATTGTTCCT	220441
rs796230414	multinucleotide-polymorphism	AGG/GGA			intron-variant	RNF152	GRCh38.p7	18:61844221	GAAGGAGGGAGGGAA[AGG/GGA]GGGAGACGGGAGGGG	220441
rs796238495	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61838864	TGCTTCTTGACCCTA[A/C]ACTGGCTACAGCACA	220441
rs796259264	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61839931	AATATTTCAGGCTCA[A/G]CTTGTATTTCCCCAT	220441
rs796394966	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61818716	ATCAGACCCAGATTC[C/T]ACCCGAAAACAACTT	220441
rs796421863	in-del	-/T			intron-variant	RNF152	GRCh38.p7	18:61823470	CCAGCTAATTTTTTT[-/T]GTATTTTTAGTAGAG	220441
rs796481717	in-del	-/A			intron-variant	RNF152	GRCh38.p7	18:61833894	AGCTTTAAAAAAAAA[-/A]GTTTCATCCACAAGA	220441
rs796504517	in-del	-/CAGTGC			intron-variant	RNF152	GRCh38.p7	18:61868875	GCATTACAAAGGCAA[-/CAGTGC]CAGTGCAAAAAGACC	220441
rs796510613	snp	A/G			intron-variant, upstream-variant-2KB	RNF152, LOC105372159	GRCh38.p7	18:61892618	TGGCTTCTTCAAAGG[A/G]AAGGTATAAAGTCAT	220441
rs796652088	in-del	G/TGT			intron-variant	RNF152	GRCh38.p7	18:61831920	TATAGTATTATGTGT[G/TGT]GGGGGGTGTGGGTGT	220441
rs796718544	multinucleotide-polymorphism	ACA/TCT			cds-indel	RNF152	GRCh38.p7	18:61813280	TCTCTCTCTCTCTCA[ACA/TCT]ACACACACACACACA	220441
rs796728909	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844109	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441
rs796730688	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61819329	TGGACCGTGGGCAGC[A/C]CCCAGTGCCAGGCCA	220441
rs796814657	snp	C/T			intron-variant	RNF152	GRCh38.p7	18:61849929	CAAGTACTGTGTGAC[C/T]TGAGGCAATTCTCAT	220441
rs796841029	snp	A/C			intron-variant	RNF152	GRCh38.p7	18:61876376	GAACTACTTTCTGAC[A/C]TGGAAGCATTATGCC	220441
rs796963429	multinucleotide-polymorphism	AC/GT			intron-variant	RNF152	GRCh38.p7	18:61839756	AAAAATTGCTGGGCG[AC/GT]GTGGTGGGTGCCTGT	220441
rs796978205	multinucleotide-polymorphism	AAA/GAC			intron-variant	RNF152	GRCh38.p7	18:61836926	GGATTACAGGCTTTG[AAA/GAC]GACAGGATATTTACA	220441
rs796991510	in-del	-/AG			intron-variant	RNF152	GRCh38.p7	18:61844101	GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA	220441

Page 1 | 2