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

RNF141

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs559929140	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10525004	GTGGCCCTGCCAAGC[C/T]ACTTTAATTTAGCAC	50862
rs559938217	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10535967	CAAGTAGCACGTGCC[C/T]GGTGCTTATGTTCTG	50862
rs560040367	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10525457	GAACAAATATTTAGT[C/T]AAACATCCTAGGAAA	50862
rs560046255	snp	A/C	0.00162975	0.0284994	synonymous-codon	RNF141	GRCh38.p7	11:10530694	AGCAGAGGAATCAGA[A/C]CCAGGTTGTACCTCA	50862
rs560058069	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512708	TGTTCCATGGAATAC[G/T]AAGAATCTATGGAGG	50862
rs560289359	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540755	TCCTCAAGCGCACCT[A/G]GACATTTAACCAACA	50862
rs560407759	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10527365	GGCCTTACAGAGAAG[C/T]TGACATTTAAGAACT	50862
rs560412562	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519603	GCCTACTACTACATA[C/T]CTAGGCTATATGGCA	50862
rs560424776	in-del	-/TA	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10517953	AAAATAGCATAAAAC[-/TA]TGAAATACTTGGGGA	50862
rs560548595	snp	A/G	0.00597247	0.0543191	intron-variant	RNF141	GRCh38.p7	11:10526731	AGGTTGCAGTGAGCC[A/G]AGATGGCGCCACTGC	50862
rs560561289	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10520983	GACATTGATAATGGG[C/T]ATATGAGTGAAAGAA	50862
rs560561381	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513383	TAGGAAAATAGTAAT[A/G]TTTGCAACTTATGAA	50862
rs560598563	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10520383	TTTCTTAAAAACTAA[C/G]ACATAACACACACAT	50862
rs560701546	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10518159	GGGGTGTAAAATGGC[A/G]CAAGACTGCTTTGGA	50862
rs560791622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10533728	TCTATTGGTATAAAA[C/T]TGAGATGCTGGGATG	50862
rs560844227	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542828	GCAAATTTGGGACAA[A/G]TTTGACCAAAGATGA	50862
rs560991855	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10528126	TAGTGGATTAAATAT[G/T]ATTTAAGGATAATCA	50862
rs561067467	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514192	CCCAGCTGTGGGAAA[A/G]CATTTCCAGAACAGC	50862
rs561242684	in-del	-/C	0.00517822	0.0506191	intron-variant	RNF141	GRCh38.p7	11:10535361	AATTGTAATTTAAAA[-/C]AAAAAACAAAAAACA	50862
rs561337941	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10528771	TTGTTCACTTAATAT[A/G]TACTGAGTTCCTACT	50862
rs561364002	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10525903	AAGGCCATTTTGAGC[C/T]TTATCAAAAAACTCG	50862
rs561440243	in-del	-/AAT			intron-variant	RNF141	GRCh38.p7	11:10530875	AAACACAAAAAGACA[-/AAT]AATAATGATTATAAT	50862
rs561452083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10522545	AGACCATCTGGGAAA[A/G]CCTCCAGTATGTAGA	50862
rs561547127	snp	A/C	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10522098	AGCATTATAAAAGAC[A/C]AATCTTTTATGTGGT	50862
rs561758048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10518176	AAGACTGCTTTGGAA[A/G]ATAGCTGGCAGCTTT	50862
rs561788180	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10536384	CTGGCACCAAGAGTT[G/T]GGCTGTTTAACATTT	50862
rs561800830	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10517522	CAAGAAGCTCAATAA[A/G]CCCCAAGCACAAGAA	50862
rs561848983	snp	C/T	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10524640	AGAAGGAAAAGAAAG[C/T]TTAGATAGAACAATA	50862
rs562002058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10525570	GGTTCAAACTTCTTA[C/T]ACAAATTTACCTCAT	50862
rs562123970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10532771	ATGCCTACGGAGTGG[A/G]TTCATATATCTTACC	50862
rs562152227	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513290	ATTGATTTGAATTTT[A/G]TTTGCTCGCCTATTA	50862
rs562213879	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10531925	ATAGGTTTAATTCTA[C/T]AGTTCTCGGAGATCA	50862
rs562272459	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	RNF141	GRCh38.p7	11:10511225	ACAGCAGGAGTTGAG[C/T]CGCGGGCGAGTGAGT	50862
rs562439700	snp	A/T	0.00438332	0.0466095	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512773	ATTAAAAAATTTTTT[A/T]AAAAAAAACGACTCC	50862
rs562561339	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10518946	CTCTCTCATACTTAA[C/T]TACAGTATTTTTGCA	50862
rs562579070	in-del	-/T	0.00159617	0.0282053	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514726	TAAAACAGTAGCAAA[-/T]TTTTAGTACCACAAA	50862
rs562726722	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10526186	AGACATAGGATGGAA[A/G]ACTGGGGAAGAAGTA	50862
rs562804483	snp	A/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10527511	TCTCACAAGAAGCCC[A/T]GAGTGTTTGGAACAG	50862
rs562836585	snp	C/T	1.6799e-05	0.00289814	intron-variant	RNF141	GRCh38.p7	11:10515110	TGCTTTCTTCTTTTT[C/T]AAAAACAGGATTTTA	50862
rs562873631	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10521787	AAATCATGTGTGTTT[A/G]TGTCTGTGTATATGT	50862
rs562920047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10521136	CACAATTCAGAGAGC[C/T]CCTGAATGAGCCATA	50862
rs562981272	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10518050	AATAAGTGGAGAAAT[A/G]TACAGCGTATGTGGA	50862
rs563004216	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514343	CAAAACACACTGCTA[A/C]AGTTATGAAATAATT	50862
rs563272788	in-del	-/T			intron-variant	RNF141	GRCh38.p7	11:10521813	ATGTAACCAGGAAGC[-/T]TGGCATGATACTTGG	50862
rs563546546	snp	A/G	0.0023933	0.0345097	intron-variant	RNF141	GRCh38.p7	11:10535693	TCCAAAAATAAACAA[A/G]AATTCCCCAAAACTT	50862
rs563689172	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10537746	AAAACATGACAAGAC[A/C]CAAGGGTTTGGGCTG	50862
rs563749434	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10523404	TTGGCTGAAATGGGC[C/T]GATAATTGTACTCCC	50862
rs563758844	snp	A/G	1.64909e-05	0.00287144	synonymous-codon	RNF141	GRCh38.p7	11:10525323	AAGTTGAATAAACTG[A/G]TATAAATTCATGATC	50862
rs563933353	snp	A/T	0.00358779	0.0422022	intron-variant	RNF141	GRCh38.p7	11:10529829	GCTCAAATGTTTATC[A/T]GAATAAACTGGAAGC	50862
rs564086112	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10524276	AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT	50862
rs564207480	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10511890	ATTTAGTATATTAGA[A/G]TGTGAAATTACATAG	50862
rs564226916	snp	A/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511359	TGCACCTTATGAGAA[A/T]CTAACTAATGCCTGA	50862
rs564415095	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10519685	CACTGTAGGCTACTG[C/T]AACACAATGGTAGGT	50862
rs564488285	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517853	TGAGTTTAATAAGGG[C/T]GCAGGATACAAGGTT	50862
rs564488992	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10532896	GAGAGGTAATATGGG[A/T]TAACAGGAAAACTGA	50862
rs564531295	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10526656	AGCATGGTGGCACAC[A/G]CCTATAGTCCCAGCT	50862
rs564669834	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540125	TAATTTAGGATCGTC[A/G]GCCGGTGGCAGCTCA	50862
rs564723830	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10532117	TATCTTTATGCTAAA[C/G]GGCAAAACTTCATAC	50862
rs564757131	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540725	CGCTCGCTCTGGCTA[C/T]GCCGCCTCAGCCCCT	50862
rs564784661	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542562	TCTGGTCAATGAAAT[A/G]AAAAAAGACAAATAT	50862
rs564832539	in-del	-/A	0.0146672	0.084371	intron-variant	RNF141	GRCh38.p7	11:10517757	AGAATTCTGAATCAG[-/A]AAAAAAGTCTTTGAA	50862
rs564940372	snp	A/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10522478	CACCTGTAGATTGGA[A/T]TATTTGGTTCTATGC	50862
rs564951129	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10534415	TATTATTGGGAGGGT[A/G]ATGAACCTCTAATTC	50862
rs565031346	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513896	GGCCAGGCTGGTCTC[A/G]AACTCCTAACCTCAA	50862
rs565098599	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10515888	TTTTCTGGCAGGGGA[A/T]GAACTCATATATGAT	50862
rs565154790	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10527712	TGTGATGTGGAATAG[A/G]CTGGTTGTTGTGCTT	50862
rs565220559	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513323	ATCCTACTATCCAGA[A/G]ATTCTGTCATCAATA	50862
rs565266249	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10528066	ATTTTTCTAATATTA[C/T]TTCCATAAAATATTC	50862
rs565284915	snp	A/C	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10515236	CTCTTTCCCAGGGGC[A/C]ACCACAGTTACCAGT	50862
rs565522371	in-del	-/AC/ACAC	0.00637749	0.0561077	intron-variant	RNF141	GRCh38.p7	11:10534479	CATGTGCATGTGTAC[-/AC/ACAC]ACACACACACACACA	50862
rs565691866	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10522772	CTCTTATAGACAAAT[C/T]ATTATGTGTCAAGCA	50862
rs565902254	in-del	-/A	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540365	CCTTTAATAAGGGGC[-/A]ATAGGGATCGATTTC	50862
rs565935762	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10522277	GAAAGAATATTCTGA[A/G]GGCTGGACTTTAAAA	50862
rs566017589	snp	C/T	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10528407	TCTAATTGCCTGTGC[C/T]TTTAGTACTTTTGTT	50862
rs566194204	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540337	GACAGTGTCAGAATA[C/T]AAAAGGTACACTACC	50862
rs566205028	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10537495	TATAAATACCTATGA[C/T]AATTTAACCAACGTG	50862
rs566296859	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10537705	AAGCTTACATAGTAG[A/T]TTGGACAAAGGAGAA	50862
rs566347425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10517715	CAACATTATTAACAT[A/G]CTGAAAGAAAAAATA	50862
rs566354532	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10519667	GCATGTTACTGTATG[G/T]AACACTGTAGGCTAC	50862
rs566416023	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542953	AGTGTGGTACATATA[C/T]GCCATGGAATACTAT	50862
rs566501646	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10515588	AATTCCCTCGCATCA[A/G]TGGAAGATTTGGTCA	50862
rs566812748	in-del	-/GCCTCGGCCTCCCAG	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10536711	TCAAGCAATCCTCCC[-/GCCTCGGCCTCCCAG]GCCGAGGATTACAGG	50862
rs566889352	snp	A/C	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10519768	TATACAAGATTAAAA[A/C]TGGTACACCTGTATA	50862
rs567004708	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10526312	CACAGGGCCATAAAA[C/T]TGTGACTTTAGGTTC	50862
rs567136509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10534552	TCTACCTTCTATAAT[C/T]TTCCTAAGAACATTT	50862
rs567394407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10536569	GCACAAAAACACATA[C/T]GTAAGATGTGCTCAA	50862
rs567466133	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541156	GCACCCTGCGGCAGC[A/G]GCTGCGCTGCCTCAG	50862
rs567489229	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10526430	GAAAATAATAGTTGT[-/A]ACACGTTTATTAATT	50862
rs567579175	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541638	TGTGTTCACCTAGCC[A/G]AGTTGTTAAGCATAA	50862
rs567639293	in-del	-/ACTA	0.00517822	0.0506191	intron-variant	RNF141	GRCh38.p7	11:10526617	TGAAACCCCATCTCT[-/ACTA]AAAGTACAAAAAATT	50862
rs567724038	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10528555	AAGAGCAACAAAAAA[C/T]GAAGGGATGAAAAGC	50862
rs567941759	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10527943	GAGAGACAAAGAAAA[A/G]CCAAGAATGACTCTA	50862
rs568082992	snp	A/C	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10516855	CACAAAAGCAAGATC[A/C]AAAAGAATCAAACTG	50862
rs568148388	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10528938	ATAAATAATGTGCTG[C/T]TGGAATCTGGAAGAG	50862
rs568307837	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10522852	CATATACTACAGTTA[G/T]CAACCTCTGTTAGAA	50862
rs568318785	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10516363	GGACAGTGATCCCTG[A/G]GACATGGGAGTCAAA	50862
rs568412718	snp	G/T	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10533840	CCCATTACATACTTT[G/T]AAAAAGCTACATAGA	50862
rs568450407	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10531287	GGCTGAGGCAGGAGC[A/T]TTGCTTGAACACGGG	50862
rs568498633	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10518452	CAACATGAATAAATA[C/T]CAAGGTAATTAGACT	50862
rs568506533	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540489	TGTAATCACTACCTT[A/C]TTATTATTAGCAAGA	50862
rs568518365	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10515241	TCCCAGGGGCAACCA[C/T]AGTTACCAGTTTCTT	50862
rs568619861	snp	A/C	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10532406	AATACATAAATACAC[A/C]CAGTAAAATGTAAAA	50862
rs568659435	snp	C/T	0.0182019	0.0936463	utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541193	GCTCAGACCTGCGGG[C/T]GGCCGCGACTCAGGC	50862
rs568739841	snp	A/G	6.66045e-05	0.00577043	intron-variant	RNF141	GRCh38.p7	11:10530768	TGAAAAGAGACAAGA[A/G]CATGTTAATTTTATG	50862
rs568778561	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10538407	ATATGACTCTGTGAT[C/G]TGCATACAATATAAA	50862
rs568928514	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542107	TTAATCTTCACAGCA[A/G]TCCTGTGAGTAGGTA	50862
rs569298728	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513499	AAATTTTAGTTCATA[A/G]GCAAAAAAAATGGTT	50862
rs569532636	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512974	CGTGTTTAAAGGTTC[C/T]GTAAGATTTTCCTTG	50862
rs569582704	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10519936	CTGTCTTTCTTGGGC[C/T]ACATATATACTAACA	50862
rs569611408	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10515505	AACAATGCAGCAATT[C/G]GCATCCCCATACCTA	50862
rs569652178	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10528319	AGATTCTTTCAGAAA[G/T]AACCTAAGGAATGCA	50862
rs569745626	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542229	CCCAAGCAGACAGAA[A/C]CCTGAACCTGTGTTT	50862
rs569779646	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514833	GATTTTCCTGTGTCT[A/G]TGCCAGTGCCACAAC	50862
rs569856990	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10529044	TTAGAGATGCAGAAA[A/T]AAAAGGTGTGGCAGA	50862
rs569910081	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10527652	GAAGTCACGGGGGGG[-/G]GGTTTTGAGCCAAGG	50862
rs569974932	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10534725	TAAAGTTACACAGCT[G/T]TAAGTGGTGAAAGTG	50862
rs570174694	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10537264	ATCTAATAAGTGTTA[C/G]AGGGATTTTTACCTG	50862
rs570203533	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10531033	TCTCAATGGTCTTTA[A/G]ATTTCTAACAAAGAC	50862
rs570251191	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10511764	CTTTTCTCCCAGATA[C/T]ATATTAGATATAAGG	50862
rs570348799	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10534218	TTTCTGTCAAATATA[C/T]AGAAAAGTTACTTTT	50862
rs570704569	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10516869	CCAAAAGAATCAAAC[A/T]GTTTCCAAGTCACTT	50862
rs570772122	snp	A/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10518503	AAAAAGCACATATTA[A/T]ATGATTCCATTTATA	50862
rs570875424	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10525662	CTTTCTCAGAGTTAA[G/T]AAATAAATTTTAGAG	50862
rs570959823	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10520020	TTAAGAAGGTTTATG[A/G]ATTTGTGTTGGGCCA	50862
rs570965671	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10527085	ACAGAAATAGCAAAG[C/T]GTATCACACTGTAAC	50862
rs571006240	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10539097	GAAATGCACAAGATC[A/G]AGGATTCCAAAAATG	50862
rs571038817	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10530887	ACAAATAATAATGAT[G/T]ATAATAACTGGATTC	50862
rs571112745	snp	A/G	0.000304847	0.0123422	intron-variant	RNF141	GRCh38.p7	11:10525173	AATAAGTGAAATACA[A/G]TACTTATGCATTATA	50862
rs571136292	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541573	CCTCCAGCCTCCCCA[C/G]TGATGATAGATACAC	50862
rs571203174	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10533240	ATTTTAAAAGCACAG[C/T]GGTCTGGGGGCATTC	50862
rs571297974	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10533962	CACAGCCATGACATA[C/T]GGGGCATACATACAA	50862
rs571452434	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540554	AGCTAGTTTGACAAG[A/G]AAAGACCTTTGGGAA	50862
rs571486306	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541027	GCGGAAGCCTGGCTC[A/G]GCAGCGGAGGGCCCT	50862
rs571634684	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10521235	AACTCAGCTCAAAAC[A/G]TCATCATCTCTCTGC	50862
rs571716181	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542293	GTAAGACTTCATTAG[C/G]GCTAGGTCCATGCCT	50862
rs571837998	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514488	CGTTGAAGTATTCTA[C/T]ATTTTCAGTCACTTA	50862
rs571933603	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513589	GAAAGAGTATTTCAA[C/T]GGAAGTACAGTGAAA	50862
rs572085857	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10523223	ACTCTCAGGCTCCTC[C/G/T]TCAAAACCACTGAGT	50862
rs572087784	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10515932	TTATGTTTTCGAAAA[C/G]GATTTTTTTCTGGTC	50862
rs572124887	in-del	-/CTAA	0.0023933	0.0345097	downstream-variant-500B	RNF141	GRCh38.p7	11:10511360	GCACCTTATGAGAAT[-/CTAA]CTAATGCCTGATGAT	50862
rs572162834	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10516920	GCTCAAGAATATTCA[C/T]AGGAATACAAAAATA	50862
rs572194428	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542633	ATTTATTTGCATAAG[A/G]AAATTGTGGAATACT	50862
rs572245854	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10527887	GCCAGATTCTGAATA[C/T]ATTTTGATGTGACAG	50862
rs572249734	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10520975	ACAATGCTGACATTG[A/G]TAATGGGCATATGAG	50862
rs572369552	snp	G/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10522481	CTGTAGATTGGAATA[G/T]TTGGTTCTATGCCTC	50862
rs572437906	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10529172	GTCAATCCTGGTTAG[G/T]CTAATCTAAACCAAT	50862
rs572474459	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10527338	GAAGGAACGCTGAGG[A/G]GTTACAGGGAAGGCC	50862
rs572550981	snp	G/T	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10536232	GGGATTAAAAAAAAA[G/T]TAGGGAAATGGCAAA	50862
rs572582177	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10537439	CATTACTTAACAAAG[-/A]AAAAAACTGAACTTT	50862
rs572636010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10535428	TATCACATTATAGAG[A/G]TAAATGAAAGGAAGT	50862
rs572664230	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10529085	TGATTATCCAAATAC[C/T]ATTCCTTCTTTTCAT	50862
rs572700504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10536741	GCCGAGGATTACAGG[C/T]ATGAGCTGCCGCACC	50862
rs572705390	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10534642	TCTTACAACAATCCT[A/G]AGAGGTAGACAATAT	50862
rs572748946	snp	A/C	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10530280	ATGAATGTATTCTTA[A/C]AAGAAATGATCTCAA	50862
rs572886036	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10528781	AATATATACTGAGTT[C/T]CTACTATGTGTAAAG	50862
rs572947920	snp	G/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10524560	AGATATTTACAAATT[G/T]AAATTATGATCATGA	50862
rs573105019	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10524039	TAAATGGAAAATACA[-/T]GTTTAACTGTAACAT	50862
rs573341106	snp	C/G	3.30797e-05	0.00406679	missense	RNF141	GRCh38.p7	11:10525212	CATCCAAAGACTAGC[C/G]TGACAAGATGTTACA	50862
rs573360493	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513711	TTGATTAGGAGTCTC[A/G]TTCTGTCTCCCAGGC	50862
rs573442458	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF141	GRCh38.p7	11:10511654	CTTGACTTCAGACAA[C/T]AGCAGTTAAAAATGC	50862
rs573504052	snp	C/T	0.00438332	0.0466095	downstream-variant-500B	RNF141	GRCh38.p7	11:10511207	TGTTAGGAACCAGGC[C/T]GCACAGCAGGAGTTG	50862
rs573523133	in-del	-/T	0.00199481	0.0315187	intron-variant	RNF141	GRCh38.p7	11:10538324	GGGCTTGACATTTAG[-/T]TTTATTTTGAAAACC	50862
rs573696158	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10535134	TTAACAACCATATCA[C/T]ATAAAGCAGGTGAAA	50862
rs573699077	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514568	TTATATCTAAGTAAA[A/G]AGATTCCAGAATACT	50862
rs573728939	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10534296	GAAAAACTAGGGATA[C/T]CTTTAAGTGAGAGTT	50862
rs573827898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10526566	AGGTGGGCAGATCAT[A/G]AGGTCAGGAGATTGA	50862
rs573891143	snp	A/T	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10526141	AAATCAGAGAAAGAT[A/T]AGAGACATGAAAGAC	50862
rs573917248	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540628	TAGATCGACGTGGCT[A/G]TTTCTGAGCTATCGT	50862
rs574037639	snp	G/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511611	TCCCTCATCTGCAAG[G/T]AGTTTTCTTATTCCC	50862
rs574138140	in-del	-/TTT	0.00159617	0.0282053	intron-variant	RNF141	GRCh38.p7	11:10524037	AATAAATGGAAAATA[-/TTT]CAGTTTAACTGTAAC	50862
rs574480333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10517052	ATAATAAAGAGAAAA[A/G]TCAATCATAACCACC	50862
rs574514576	snp	A/T	0.0134861	0.0810011	intron-variant	RNF141	GRCh38.p7	11:10526498	ACTCAAGAATGAGTC[A/T]TGCGGCCAGGCACGG	50862
rs574766510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10516625	CTGATCAGTGTGTGC[A/G]TGTGAAGACACTACC	50862
rs574927976	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10531135	TAATCCCAGCACTTT[A/G]GGAGGCCAAGGCAGG	50862
rs575039039	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10523338	CTGAATGTGAGTCTT[C/G]GCTAGAACAATTTCT	50862
rs575047443	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10524007	CAAGTAATTCTATTA[A/G]AGATAATTGGGAAAT	50862
rs575113062	snp	A/G			downstream-variant-500B	RNF141	GRCh38.p7	11:10511239	GCCGCGGGCGAGTGA[A/G]TATTATTGCCTGAGC	50862
rs575127839	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10524728	CCTTCTGGTAACTAA[C/G]TATATGCATTCGGTT	50862
rs575272956	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10518716	TTCCTTCTAAACACA[C/T]ACACAGAATAAATGT	50862
rs575306687	snp	A/C/T	3.29588e-05	0.00405938	missense	RNF141	GRCh38.p7	11:10525301	CTTGACTTGTGATAT[A/C/T]TTTATAAAGTTGAAT	50862
rs575653888	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541351	CAGATGGTCATCTGA[A/G]ACGAGAGGTGGCGGC	50862
rs575702489	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540690	AGCCCGGCGGAGACC[A/G]AGCCCGCGGGCCACC	50862
rs575735519	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10519326	ATATATTAGGGAAAA[A/T]GTATTAAGAGGGCTA	50862
rs575811771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10532854	TGAACTGCTAGTCGA[C/T]TTCATTCAGCCTTTT	50862
rs575890986	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10511814	ATGAATTTTAAAACA[G/T]CACACAAACATCACA	50862
rs575933631	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513801	TCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA	50862
rs576229902	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10520830	TTAGCTCCATTATAA[A/T]CTTGAGACCACCATC	50862
rs576294516	snp	A/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10536153	GGACTTGACCTAGTT[A/T]TGTATCAGGGAAGAA	50862
rs576296456	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10527974	AGAAGTTGGTCTAAG[A/G]AAAAAGAAGGATGAA	50862
rs576361527	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10521827	GCTGGCATGATACTT[A/G]GGTATGGAAAACTGA	50862
rs576411267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10515823	ACAGGAAGACTTATA[C/T]AAAAATGGAGCATAC	50862
rs576499147	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10522390	TACAAAGTTCTCTTA[A/G]CTTTTTGCTACCTTC	50862
rs576528086	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10521511	AGACTATAAACTTCT[A/T]AAGGATAGGAGCTAT	50862
rs576605716	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541985	CTTCACCAGTCACTT[A/G]TAGATTCACCTTGTG	50862
rs576752776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10536921	TGAAAAGTCTGTATT[C/T]AGCTCTAAGCAGTTG	50862
rs576876419	snp	C/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10537786	ATCACAGAAAAGTGA[C/G]TAGGAAGATAAGGGT	50862
rs576884509	in-del	-/TGTG	0.00199481	0.0315187	intron-variant	RNF141	GRCh38.p7	11:10533558	ATATATATATATGCA[-/TGTG]TGTGTCTATATACAC	50862
rs576965390	snp	A/G	0.00517822	0.0506191	intron-variant	RNF141	GRCh38.p7	11:10529968	CTTTATGGGTCAGTC[A/G]GGAATGAACTTCAGA	50862
rs576980679	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10530050	CTTTGTTTTAGAGCC[A/G]GGGTGGGGATAGGAG	50862
rs576981442	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10516443	CCCCTGATCAAGAAG[C/T]GGGAAGCTTGATGGA	50862
rs577013551	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10529221	TCTGTCAGTGTAGGT[A/G]TATGAAGGGGATATG	50862
rs577360178	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10519510	TAAAGACAGAGATAC[A/G]GTCTGAGAAACTCAT	50862
rs577418220	snp	C/T	0.00119737	0.0244387	intron-variant	RNF141	GRCh38.p7	11:10517960	CATAAAACTATGAAA[C/T]ACTTGGGGATAGATG	50862
rs577503771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10517291	GAAAAATGGTGAATA[C/T]GAAAAGAGATAGCAA	50862
rs577546013	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10518791	TTAGACTTAAGTCAG[C/G]CACAAATTTTCATAC	50862
rs577654356	snp	C/T	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10524379	GAGATCGCGCCTGGG[C/T]GACAGAGCAAGACTC	50862
rs577787106	snp	C/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10538868	TTAACAAGATACTCC[C/G]CCCTAGGCCATGCAA	50862
rs577985996	in-del	-/A	0.00438332	0.0466095	intron-variant	RNF141	GRCh38.p7	11:10537669	AGAAAAATAAGGACT[-/A]AAAAAAGTAATTAAG	50862
rs577990878	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541382	GAAGGAGAGTCTCGC[C/T]TGTCACGCTCCCGGA	50862
rs578035753	snp	C/T	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10534250	CATATTATACAAAAA[C/T]GGCAATATACTCATT	50862
rs578118406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10527331	CAGGGGAGAAGGAAC[A/G]CTGAGGGGTTACAGG	50862
rs578120547	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513186	AGCTATTTGGTACTT[A/G]GCTGTCCCATTATGA	50862
rs578146172	snp	A/G	0.000798403	0.0199641	intron-variant	RNF141	GRCh38.p7	11:10526714	CTTGAACCAGGAGGC[A/G]GAGGTTGCAGTGAGC	50862
rs745386395	snp	C/T	3.30147e-05	0.00406279	synonymous-codon	RNF141	GRCh38.p7	11:10530748	AGAAGCCACTTTAGC[C/T]GTTCTGAAAAGAGAC	50862
rs745444712	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10538231	CTTCATCACTAACTC[C/T]TTGCATTAAAATGCA	50862
rs745492048	snp	A/G	6.65868e-05	0.00576966	intron-variant	RNF141	GRCh38.p7	11:10533999	GAAAAACGAAAAACA[A/G]AAAGAGCAAGCCTTA	50862
rs745524140	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10536850	TCTTGCTAGAAGCAG[G/T]TATCTTGAGCAAGCA	50862
rs745782476	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542220	AGATTCAAACCCAAG[C/T]AGACAGAACCCTGAA	50862
rs746383913	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10529051	GCAGAAATAAAAGGT[-/G]GTGGCAGAAACTACT	50862
rs746410045	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10527488	TACCTGGCAAGGAGC[A/T]CAGAGAGTCTCACAA	50862
rs746518564	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10529333	AGGATTTCTTGATAA[C/G]TGAGAAAATAAGTAT	50862
rs746526993	snp	A/C	4.94328e-05	0.00497131	synonymous-codon	RNF141	GRCh38.p7	11:10534084	ACTCTCTCGAACCAA[A/C]GTAACATGTTTTGCT	50862
rs746577503	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10535774	AGAAAAAAAGTCTTT[C/T]CCAAGAAGGGCAGTA	50862
rs746615344	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10515367	CTTACAGACTAGTAT[G/T]TATCAGCACCTGTTA	50862
rs746632453	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10529953	CCTAACCCAGGGAAT[C/G]TTTATGGGTCAGTCG	50862
rs746704802	snp	C/T	1.72716e-05	0.00293862	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514883	ACCAAATATTTGAGC[C/T]CACAATAGCAACAGA	50862
rs746867224	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10538893	ATGCAACAGTGGTAT[G/T]GCATAGAAACATAAT	50862
rs746949245	snp	C/G			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541481	GAGCGGAAAGTGGAG[C/G]GCCCCGCTGGCGACC	50862
rs747148051	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10532763	TGGTTGTAATGCCTA[C/T]GGAGTGGGTTCATAT	50862
rs747235846	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10531307	TTGAACACGGGAGGT[A/G]AAGGTTGTAGTGAGC	50862
rs747268789	in-del	-/C			intron-variant	RNF141	GRCh38.p7	11:10537339	CAAAATGAAACTGAA[-/C]CTTCCTCTAACATTC	50862
rs747384409	snp	A/G	1.65444e-05	0.00287609	intron-variant	RNF141	GRCh38.p7	11:10530612	ACCAAAATAGCTTAA[A/G]CTCAGAGGTAGAAGT	50862
rs747432971	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10536764	GCCGCACCCGGCCAA[A/G]TCTGGGGTTTTTAAT	50862
rs747477029	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10525997	TCCAGTTTACAATCT[A/C]ATGTAGAAGATACTT	50862
rs747691737	snp	G/T	1.70956e-05	0.00292361	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514900	ACAATAGCAACAGAA[G/T]ACTTTCACTTCAAGG	50862
rs747795634	snp	C/T			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541256	CCCGCCCCCCGCGCG[C/T]TGCCGGGAGACGGCG	50862
rs747831121	in-del	-/ACACA			intron-variant	RNF141	GRCh38.p7	11:10532529	CACACACACACACAC[-/ACACA]CACACCCCACAACTA	50862
rs747846574	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10529064	GGTGTGGCAGAAACT[A/G]CTGGCTGATTATCCA	50862
rs747848258	in-del	-/ATTT			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512355	CAAAGAGCTGTGCTC[-/ATTT]ATTTATTTGATAAGG	50862
rs748033790	snp	A/G/T	3.29534e-05	0.00405904	missense	RNF141	GRCh38.p7	11:10534093	AACCAACGTAACATG[A/G/T]TTTGCTACTTTTTCT	50862
rs748060732	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10520281	ACAACACTTACCTTA[A/C]AACACACATTATACA	50862
rs748123268	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10527413	GTCATATAGATGTCT[A/C]GGGGGAAGATCATTC	50862
rs748185271	snp	A/C	1.65015e-05	0.00287237	synonymous-codon	RNF141	GRCh38.p7	11:10519093	GATGAGGTCAGCCCG[A/C]CCATCCATACAGATA	50862
rs748251582	in-del	-/CAG			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542720	CAAATATACAAAAAT[-/CAG]TTGTATTTCTATATA	50862
rs748390952	snp	C/T	1.81168e-05	0.00300966	intron-variant	RNF141	GRCh38.p7	11:10519188	TATTCTCTGTCATTA[C/T]GCTTTATACTTTTTG	50862
rs748405729	snp	C/T	1.64765e-05	0.00287019	missense	RNF141	GRCh38.p7	11:10525279	CTCTGTGCCAATACT[C/T]CTGCTGCTTGACTTG	50862
rs748458528	in-del	-/AAA			intron-variant	RNF141	GRCh38.p7	11:10535464	AGGAAGATCCAGGCC[-/AAA]AAAAAAAAAAAAAAT	50862
rs748572607	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10533983	ATACATACAACAAGG[A/G]GAAAAACGAAAAACA	50862
rs748580342	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10536485	TCTAGTGAATAATAG[C/G]ATCAAGACTAAAACA	50862
rs748628351	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10516398	GTGAGACCTATACTT[C/G]CCTCAGCTTACAGCC	50862
rs748739530	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512211	TTTAAAAAAGACAAA[A/G]CTGTACAGAATACAA	50862
rs748787045	in-del	-/AC			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10539685	TGATCAGAAAAAGAT[-/AC]ACATACATATATATT	50862
rs748827871	snp	C/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511226	CAGCAGGAGTTGAGC[C/T]GCGGGCGAGTGAGTA	50862
rs748853248	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10527706	TCAAATTGTGATGTG[A/G]AATAGGCTGGTTGTT	50862
rs748902382	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10538535	ATATTTCTATCATAC[C/T]ATGACATTCGTTAAG	50862
rs748945807	snp	C/G	1.64776e-05	0.00287028	missense	RNF141	GRCh38.p7	11:10530714	GTTGTACCTCAAAGA[C/G]AAGATGTTTTTCCTG	50862
rs748955278	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10526434	ATAATAGTTGTAACA[C/T]GTTTATTAATTGCTT	50862
rs748971316	snp	C/T			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540113	CATGGAGGTGACTAA[C/T]TTAGGATCGTCGGCC	50862
rs749176406	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10538676	CCATTGGCAGTTTTT[-/G]TTTTATTATTATTCA	50862
rs749397617	snp	A/G	4.9436e-05	0.00497148	synonymous-codon	RNF141	GRCh38.p7	11:10525299	TGCTTGACTTGTGAT[A/G]TCTTTATAAAGTTGA	50862
rs749443495	in-del	-/TATT			intron-variant	RNF141	GRCh38.p7	11:10524035	ATAATAAATGGAAAA[-/TATT]TACAGTTTAACTGTA	50862
rs749501156	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10518951	TCATACTTAACTACA[A/G]TATTTTTGCACTTTT	50862
rs749519214	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10528763	GATTTTTTTTGTTCA[C/T]TTAATATATACTGAG	50862
rs749568169	in-del	-/C			intron-variant	RNF141	GRCh38.p7	11:10529183	TTAGTCTAATCTAAA[-/C]CAATCATGCTAATCA	50862
rs749763401	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512956	GGTATGTGTGTATGC[A/G]CACGTGTTTAAAGGT	50862
rs749839722	snp	C/T	1.70426e-05	0.00291908	intron-variant	RNF141	GRCh38.p7	11:10525164	ATATTAGAAAATAAG[C/T]GAAATACAATACTTA	50862
rs749842573	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541655	GTTGTTAAGCATAAG[A/G]GAATGTATGAAAAGT	50862
rs749842665	in-del	-/CACACACC			intron-variant	RNF141	GRCh38.p7	11:10532532	ACACACACACACACA[-/CACACACC]CCACAACTATATACA	50862
rs749954833	in-del	-/AT			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514415	ACCACAAGGGGGCAT[-/AT]ATATATATATACTCC	50862
rs749978265	snp	A/C	1.64958e-05	0.00287187	synonymous-codon	RNF141	GRCh38.p7	11:10525227	CTGACAAGATGTTAC[A/C]GAGGATGAGTTTTCA	50862
rs750063039	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10533639	CCTTTGACTATCCTA[A/G]GAGTCTTTCTCTAGA	50862
rs750128344	snp	C/T	1.64789e-05	0.0028704	missense	RNF141	GRCh38.p7	11:10534071	AAGTTAAGGAGCCAC[C/T]CTCTCGAACCAACGT	50862
rs750131395	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10522828	AATTCTCTCAAAAAT[A/C]CTATAAAGCATATAC	50862
rs750172992	in-del	-/AAAC			intron-variant	RNF141	GRCh38.p7	11:10535687	ACAGTTTCCAAAAAT[-/AAAC]AAAAATTCCCCAAAA	50862
rs750306245	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10525473	AAACATCCTAGGAAA[C/T]AGGAGTTTTCAGGAT	50862
rs750357608	snp	C/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511267	AGCTCCACCTCCTGT[C/T]AGATCAGCAGCGGTA	50862
rs750427906	snp	C/T	1.66319e-05	0.00288369	missense	RNF141	GRCh38.p7	11:10519140	CGGTCAGCTGCTTCA[C/T]CCTGCAATGTGAAAA	50862
rs750634188	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529669	AATCTCACAGCAGCA[C/T]AAATTAGAATTTGGA	50862
rs750689044	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10528177	AGAAAAAGACTTAAT[A/G]TAAATACAGAGGGTT	50862
rs750812787	snp	A/G	8.24232e-05	0.0064191	missense	RNF141	GRCh38.p7	11:10514989	TCATCTTCAGTGGGT[A/G]CATCTGATACCACCC	50862
rs750953791	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541127	CGGAGCTCACCCCAG[G/T]TTCAAGGCATCGCGC	50862
rs751010835	in-del	-/AA			intron-variant	RNF141	GRCh38.p7	11:10535465	GGAAGATCCAGGCCA[-/AA]AAAAAAAAAAAAAAT	50862
rs751050206	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10532041	AAAAGGAAGACCTCT[A/G]TATCACACAGTAAGC	50862
rs751201683	snp	A/G	1.66147e-05	0.0028822	utr-variant-5-prime	RNF141	GRCh38.p7	11:10534199	AGAGTGTTGCTTCAC[A/G]TAGTTTCTGTCAAAT	50862
rs751247536	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10534726	AAAGTTACACAGCTG[G/T]AAGTGGTGAAAGTGA	50862
rs751262945	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542708	AAGATACAAAATCAA[A/G]TATACAAAAATCAGT	50862
rs751287429	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10525175	TAAGTGAAATACAAT[A/G]CTTATGCATTATATA	50862
rs751337438	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10532529	CACACACACACACAC[-/A]CACACACACCCCACA	50862
rs751433491	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10536273	TCCAGGCAGAGGTTA[C/T]GAAAAGTGCCTGAGA	50862
rs751521793	snp	C/T	1.65875e-05	0.00287984	synonymous-codon	RNF141	GRCh38.p7	11:10525350	GATCCGTGATGCCTC[C/T]ACAATGCCACTGCTT	50862
rs751633199	snp	A/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513960	GGATTACAGGTGTGA[A/T]CCACTGCACTGGCCT	50862
rs751775158	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10511962	TTATTTATTGCACAA[C/T]TTATCAGTGGGTACT	50862
rs751787351	snp	A/G			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540829	AACAACCGTTTTGGG[A/G]TAGAGAAGGAAAAAC	50862
rs751838530	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10528034	CACCTTAGTACCTAG[C/T]TTTTAATTAATCTCT	50862
rs751865414	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512692	CAAGGTTTTCAAAAT[A/G]TGTTCCATGGAATAC	50862
rs751935601	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10539146	GGTACATAGTGAATC[A/G]CTTATTTTTCTAACA	50862
rs752093434	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10518730	ATACACAGAATAAAT[A/G]TAGAAATGAGGAGAA	50862
rs752122241	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537827	AGGCTTCTTTGAACA[C/T]ATTTCTCTCAGCTTT	50862
rs752155868	snp	A/G	0.000188129	0.00969686	intron-variant	RNF141	GRCh38.p7	11:10532018	GAAATATCCTGTGCT[A/G]AATAAATAAAAGGAA	50862
rs752172840	snp	A/G			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541364	GAGACGAGAGGTGGC[A/G]GCGAAGGAGAGTCTC	50862
rs752213427	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529837	GTTTATCTGAATAAA[C/T]TGGAAGCAAAACACA	50862
rs752292152	snp	C/T	4.94556e-05	0.00497246	missense	RNF141	GRCh38.p7	11:10515034	CCAGTCATCTGTAGG[C/T]GACAAATAGGGCAAT	50862
rs752303576	snp	G/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541849	TTGTTTAAGTCGTCT[G/T]GTCAAAGTTGCCTAG	50862
rs752337110	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10523475	ACACTCATCACAATT[C/G]TATACCCTGTAAGTA	50862
rs752371027	in-del	-/AGA			intron-variant	RNF141	GRCh38.p7	11:10527492	TGGCAAGGAGCACAG[-/AGA]GTCTCACAAGAAGCC	50862
rs752418870	snp	A/C/G	1.64765e-05	0.00287019	missense	RNF141	GRCh38.p7	11:10530686	TTCCAAAAAGCAGAG[A/C/G]AATCAGACCCAGGTT	50862
rs752425130	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10521688	ATATATCTCAAACTT[C/G]TTGAAATGATGAGAT	50862
rs752560195	snp	C/T	3.3e-05	0.00406189	intron-variant	RNF141	GRCh38.p7	11:10530639	AAGTCTCCATCAGTC[C/T]CACCTTGGTACAGAC	50862
rs752741404	snp	C/G/T	8.84907e-05	0.0066512	intron-variant	RNF141	GRCh38.p7	11:10519182	CAATTATATTCTCTG[C/G/T]CATTATGCTTTATAC	50862
rs752754763	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10527144	GTATTTATTGAGTAC[C/G]ATTATGTGGATGTTA	50862
rs752934581	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10537681	ACTAAAAAAAGTAAT[A/T]AAGGCCAAAAGCTTA	50862
rs752951246	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10518584	GTACATTAAATACAT[G/T]TAGTTTATTGTATGT	50862
rs752968810	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10532319	TGCTTTGCACACTAC[C/T]CTTTGGATAATTTTT	50862
rs753031326	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10523036	ACTTCATAGTGATTA[C/G]AGCCATCTGAGTATG	50862
rs753084338	snp	A/G	6.60055e-05	0.00574442	synonymous-codon	RNF141	GRCh38.p7	11:10534062	ATTCTTCATAAGTTA[A/G]GGAGCCACTCTCTCG	50862
rs753173942	in-del	-/A	1.64784e-05	0.00287035	frameshift-variant	RNF141	GRCh38.p7	11:10534068	ATAAGTTAAGGAGCC[-/A]ACTCTCTCGAACCAA	50862
rs753307128	snp	C/G	1.72564e-05	0.00293733	intron-variant	RNF141	GRCh38.p7	11:10518990	ATTCATGTACACTAT[C/G]CCACTGACCTTGGCC	50862
rs753311836	snp	A/C	1.64936e-05	0.00287168	missense	RNF141	GRCh38.p7	11:10534143	ACTGTGTCTGATCCG[A/C]AATTTGCTGTCCCAT	50862
rs753325775	in-del	-/A			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542714	CAAAATCAAATATAC[-/A]AAAATCAGTTGTATT	50862
rs753341964	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541172	GCTGCGCTGCCTCAG[C/T]CCACAGCTCAGACCT	50862
rs753409216	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10534620	TCCGTATATTATGTC[A/C]ATTACTTCTTACAAC	50862
rs753732698	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533775	AATTGCTTCAATATG[C/T]CTGTGCTGTGTTCCA	50862
rs753757643	in-del	-/GAG			intron-variant	RNF141	GRCh38.p7	11:10526023	TACTTGGGGCAAGCA[-/GAG]GAGATTGCTTTCACA	50862
rs753792032	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517881	GTTGATATACAAATA[C/T]CTATTGTATTTCCAT	50862
rs753804822	in-del	-/AGA			intron-variant	RNF141	GRCh38.p7	11:10522864	TTATCAACCTCTGTT[-/AGA]AGATGAGGAAACTGA	50862
rs753881944	snp	A/G			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540969	CGTCCCCACGCCCCA[A/G]TCCGAGGCCCGGGGA	50862
rs753885389	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541244	TGACGCAAAGCCCCG[-/C]CCCCCCGCGCGTTGC	50862
rs754000040	snp	C/T	1.90369e-05	0.00308514	intron-variant	RNF141	GRCh38.p7	11:10525410	AAAAGAAAAGTTGAT[C/T]ATTTCTCTGACCAAT	50862
rs754014752	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10524087	TGGTTAAGAATGAAC[A/C]AGAAAATGCAACTGT	50862
rs754034163	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10537510	TAATTTAACCAACGT[A/G]GTATAGGGGAGATAG	50862
rs754126468	snp	C/T	3.29669e-05	0.00405984	synonymous-codon	RNF141	GRCh38.p7	11:10530658	CTTGGTACAGACCAC[C/T]CGTACAACCACTTTC	50862
rs754134903	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10520045	GGGCCACATTAAAGC[A/G]ATCCTGGGCTGCATG	50862
rs754174618	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542715	AAAATCAAATATACA[A/T]AAATCAGTTGTATTT	50862
rs754222998	snp	A/G	1.65468e-05	0.00287631	utr-variant-5-prime	RNF141	GRCh38.p7	11:10534167	GTCCCATGATGAAAA[A/G]ATGTCTTTCAAAATC	50862
rs754291072	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10533963	ACAGCCATGACATAT[-/G]GGGCATACATACAAC	50862
rs754361550	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529810	TAATGCCTCTCACAC[C/T]TGTGCTCAAATGTTT	50862
rs754526192	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10535856	TTATTTTTCTTGATC[A/G]AATCCAAACTTATGA	50862
rs754580207	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10538892	CATGCAACAGTGGTA[C/T]TGCATAGAAACATAA	50862
rs754607082	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10521605	CTTAAAATTTTGATT[C/T]GAATGTAAAAATAAA	50862
rs754714422	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533798	GTGTTCCAAGTTCCA[C/T]TTTAAGTTCTTTCCA	50862
rs754785956	in-del	-/ACACAC			intron-variant	RNF141	GRCh38.p7	11:10532499	TAGTTCATTTTCTAC[-/ACACAC]ACACACACACACACA	50862
rs754791993	snp	A/G	0.000378941	0.0137596	missense	RNF141	GRCh38.p7	11:10525255	TCATCAGGTTCTTCA[A/G]AGGTGGAGCTCTGTG	50862
rs754999415	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10524136	AAAGAAACCACTGGC[C/T]GGGCATGGTGGCTCA	50862
rs755065262	snp	G/T	1.64803e-05	0.00287052	missense	RNF141	GRCh38.p7	11:10534051	TCTCCCAAGAAATTC[G/T]TCATAAGTTAAGGAG	50862
rs755141845	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10530499	AAACAGCTAGTTAGA[A/G]GGCAATAACAGTAAC	50862
rs755277333	in-del	-/ACA			intron-variant	RNF141	GRCh38.p7	11:10532535	CACACACACACACAC[-/ACA]CCCCACAACTATATA	50862
rs755311802	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10522913	GTCAAAAAAATCACA[C/T]AGGAGTGGAGCCAGG	50862
rs755418142	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514834	ATTTTCCTGTGTCTG[C/T]GCCAGTGCCACAACC	50862
rs755454354	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542716	AAATCAAATATACAA[A/G]AATCAGTTGTATTTC	50862
rs755522471	snp	A/G	1.68502e-05	0.00290255	intron-variant	RNF141	GRCh38.p7	11:10533974	ATATGGGGCATACAT[A/G]CAACAAGGGGAAAAA	50862
rs755688499	snp	A/G	0.000121683	0.00779915	intron-variant	RNF141	GRCh38.p7	11:10518981	TCAAAGTTTATTCAT[A/G]TACACTATCCCACTG	50862
rs755704389	snp	A/G	3.29734e-05	0.00406025	missense	RNF141	GRCh38.p7	11:10515035	CAGTCATCTGTAGGC[A/G]ACAAATAGGGCAATT	50862
rs755709112	in-del	-/ACACACA			intron-variant	RNF141	GRCh38.p7	11:10532531	CACACACACACACAC[-/ACACACA]CCCCACAACTATATA	50862
rs755768413	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10518836	GTCAAAACTAAGGTA[C/T]ACCCCCATATTTAAT	50862
rs755835613	in-del	-/AAAA			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542790	ATCTCTTATCAGCAA[-/AAAA]AAAAAAAAAAAAAAA	50862
rs755861355	snp	A/G	5.41355e-05	0.00520239	intron-variant	RNF141	GRCh38.p7	11:10525395	ATACAAAGAACATGA[A/G]AAAGAAAAGTTGATC	50862
rs755890512	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10532222	AGTTGAAAATATAAA[C/G]ATAACAAAGCATTCC	50862
rs755956342	snp	A/C			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512140	AACCACTTCACAAAT[A/C]CTAGAAGGCACACAT	50862
rs756062866	in-del	-/AG			intron-variant	RNF141	GRCh38.p7	11:10518016	AAAAAAATTGGTGAC[-/AG]AAATTAAAGAAGACC	50862
rs756186913	in-del	-/TGAGCCAAGATCACGCCATTGCACTCCAGCC			intron-variant	RNF141	GRCh38.p7	11:10531318	AGGTGAAGGTTGTAG[lengthTooLong]TGGGCGACAGAGTGA	50862
rs756214541	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10528399	AAAAAATATCTAATT[A/G]CCTGTGCCTTTAGTA	50862
rs756227301	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10522144	ATACGTTAGTAACAG[A/G]GAAAAGAGGGAAGTC	50862
rs756239252	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10515997	TTGAGCCAGAGACAT[A/C]TTATGCAGAGAAAAA	50862
rs756302960	snp	A/G	1.64762e-05	0.00287016	missense	RNF141	GRCh38.p7	11:10525282	TGTGCCAATACTCCT[A/G]CTGCTTGACTTGTGA	50862
rs756363942	snp	C/T	1.67464e-05	0.0028936	intron-variant	RNF141	GRCh38.p7	11:10533990	CAACAAGGGGAAAAA[C/T]GAAAAACAAAAAGAG	50862
rs756440181	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542713	ACAAAATCAAATATA[C/T]AAAAATCAGTTGTAT	50862
rs756454511	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10528390	AATCACATGAAAAAA[C/T]ATCTAATTGCCTGTG	50862
rs756557395	snp	A/G	1.64795e-05	0.00287045	missense	RNF141	GRCh38.p7	11:10534064	TCTTCATAAGTTAAG[A/G]AGCCACTCTCTCGAA	50862
rs756690276	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10527726	GCTGGTTGTTGTGCT[-/G]TGGAATAGACTGCTT	50862
rs756787555	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10517642	GCACATTACCTACAG[A/C]GGAAAAAAGGATGAC	50862
rs756787742	snp	A/G	1.68151e-05	0.00289953	intron-variant	RNF141	GRCh38.p7	11:10519012	ACCTTGGCCCAGCCC[A/G]TGAATGCAGTAGGTA	50862
rs756826746	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10532089	TTATAGGGTACATTT[A/T]ATCTAATACCTGTAT	50862
rs756839079	snp	C/T	1.65474e-05	0.00287636	missense	RNF141	GRCh38.p7	11:10519125	AACACTCCTCCTCAT[C/T]GGTCAGCTGCTTCAC	50862
rs756854429	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10519756	GTGTAAATACGGTAT[A/G]CAAGATTAAAAATGG	50862
rs756916617	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10531019	TTGTCACACCTATAT[C/G]TCAATGGTCTTTAAA	50862
rs757026936	in-del	-/ACACACA			intron-variant	RNF141	GRCh38.p7	11:10532529	CACACACACACACAC[-/ACACACA]CACCCCACAACTATA	50862
rs757085086	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10533206	ACCAAGGGAGAAAAT[-/A]AAATAGCAAAAAAGT	50862
rs757337246	snp	A/G	1.65817e-05	0.00287933	intron-variant	RNF141	GRCh38.p7	11:10530594	TTAAATATAGTTCTA[A/G]CCACCAAAATAGCTT	50862
rs757360625	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533852	TTTTAAAAAGCTACA[C/T]AGAAAGTCAACTTAT	50862
rs757371663	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10524404	GACTCCGCCTCAATT[-/A]AAAAAAAAAAAAATC	50862
rs757384031	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10525800	TCTTAAATATCTTTA[A/G]GTTCTATTTTGTACC	50862
rs757468754	snp	A/C/G	3.29616e-05	0.00405954	missense	RNF141	GRCh38.p7	11:10530660	TGGTACAGACCACCC[A/C/G]TACAACCACTTTCCA	50862
rs757506564	snp	C/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512720	TACTAAGAATCTATG[C/G]AGGAGATACAGGGTT	50862
rs757552571	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10526060	TTGGGGAGCCATGGA[C/G]TGAGGCATAATGAAA	50862
rs757638442	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537973	TTACATCTGCTGCTT[C/T]TCAATGTGCTTTTAA	50862
rs757700012	snp	A/G	1.73381e-05	0.00294427	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514867	ACATTCTTCCCCCAT[A/G]ACCAAATATTTGAGC	50862
rs757887723	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10530805	CATATATTAATAAAA[C/T]AATACAGCCATGAAA	50862
rs758023447	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	RNF141	GRCh38.p7	11:10534075	TAAGGAGCCACTCTC[C/T]CGAACCAACGTAACA	50862
rs758058858	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541873	TGCCTAGACAATAAA[C/T]AGCAGAGCAAGGATT	50862
rs758189193	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10521723	AAACAATAGGATTTT[A/C]ATAGAAGACATTCTA	50862
rs758252584	snp	A/T	0.000301836	0.0122812	intron-variant	RNF141	GRCh38.p7	11:10530774	GAGACAAGAACATGT[A/T]AATTTTATGAAAAAT	50862
rs758276878	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10520347	TTTAAGATTTATTTA[C/G]TTTTTTACTTTCTAA	50862
rs758287949	snp	C/G/T			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541340	GCTTTCGAGCCCAGA[C/G/T]GGTCATCTGAGACGA	50862
rs758345406	snp	A/G	1.64768e-05	0.00287021	missense	RNF141	GRCh38.p7	11:10530680	ACCACTTTCCAAAAA[A/G]CAGAGGAATCAGACC	50862
rs758549989	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10527170	TGTTATTGGTACTAT[A/G]TGCACTGCTCTAGGC	50862
rs758605995	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542766	ATTAGAAATGGAAAA[A/T]TTTTAAATATCTCTT	50862
rs758632897	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10525863	TAAAATAAATCCTAA[C/G]AAAAGGTGGTTGGAC	50862
rs758726327	snp	A/T	1.64814e-05	0.00287061	missense	RNF141	GRCh38.p7	11:10515009	TGATACCACCCAAGA[A/T]TCATTTGCTCCAGTC	50862
rs758737480	in-del	-/CTGTGT	6.59217e-05	0.00574078	cds-indel	RNF141	GRCh38.p7	11:10534129	CTTGTTAATAACCAA[-/CTGTGT]CTGATCCGAAATTTG	50862
rs758821193	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10537765	GGGTTTGGGCTGGGC[A/C]AGTTAATCACAGAAA	50862
rs758886715	in-del	-/ATAAATTTTCAGAAGCC			intron-variant	RNF141	GRCh38.p7	11:10523239	CAAAACCACTGAGTA[-/ATAAATTTTCAGAAGCC]ATAAATTTTCAGAAG	50862
rs758916922	snp	C/T	4.95274e-05	0.00497607	intron-variant	RNF141	GRCh38.p7	11:10530633	AGGTAGAAGTCTCCA[C/T]CAGTCTCACCTTGGT	50862
rs759141160	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10535846	CACATTGTCCTTATT[C/T]TTCTTGATCGAATCC	50862
rs759147605	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10524526	ACATGTTTGGACCCA[C/T]GTAAATCTTTTTCCA	50862
rs759340238	in-del	-/ACACACCCCA			intron-variant	RNF141	GRCh38.p7	11:10532533	CACACACACACACAC[-/ACACACCCCA]CAACTATATACAGCT	50862
rs759364181	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10534660	AGGTAGACAATATTA[A/C]ACCCCTACCTATTTC	50862
rs759473036	in-del	-/CTG			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542701	AGTTGCAAGATACAA[-/CTG]AATCAAATATACAAA	50862
rs759489677	snp	C/T	1.66607e-05	0.00288619	missense	RNF141	GRCh38.p7	11:10525357	GATGCCTCCACAATG[C/T]CACTGCTTTTGTTAA	50862
rs759531642	in-del	-/TAT			intron-variant	RNF141	GRCh38.p7	11:10526387	TTACATATTTTAAAA[-/TAT]TATTATACATTTGAA	50862
rs759558630	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10531762	CTCTCTCTGAGCACC[A/G]GTGGGGATATCACAC	50862
rs759560807	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10515378	GTATGTATCAGCACC[G/T]GTTAGAGCTGTTTAT	50862
rs759615126	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10532101	TTTTATCTAATACCT[A/G]TATCTTTATGCTAAA	50862
rs759822727	snp	A/T	1.68369e-05	0.0029014	intron-variant	RNF141	GRCh38.p7	11:10525180	GAAATACAATACTTA[A/T]GCATTATATACCTTC	50862
rs759889086	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10530483	GACAACTGTAAGATT[C/G]AAACAGCTAGTTAGA	50862
rs759938476	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10517276	AAGTTAGACATTGAA[A/G]AAAAATGGTGAATAT	50862
rs759980419	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10515811	GGCTCATAAGCAACA[-/G]GAAGACTTATATAAA	50862
rs759997030	snp	A/G			downstream-variant-500B	RNF141	GRCh38.p7	11:10511498	CTGCTACAGCAGGGT[A/G]AATAGACATACGAAC	50862
rs760009984	in-del	-/A	1.65097e-05	0.00287308	frameshift-variant	RNF141	GRCh38.p7	11:10525333	AACTGGTATAAATTC[-/A]TGATCCGTGATGCCT	50862
rs760099219	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10534407	CACTTATATATTATT[A/G]GGAGGGTGATGAACC	50862
rs760113345	in-del	-/AG			intron-variant	RNF141	GRCh38.p7	11:10527490	CCTGGCAAGGAGCAC[-/AG]AGAGTCTCACAAGAA	50862
rs760307256	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10521331	CATAAACTGTAAGCT[C/T]TTTGAATATAGGGTG	50862
rs760313111	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533717	TCAAACAAGAGTCTA[C/T]TGGTATAAAATTGAG	50862
rs760333195	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10524981	GTGACAGAAACATTA[A/G]TATTAAAGTGGCCCT	50862
rs760371233	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10517696	AAACAAGATGAGTGT[G/T]AAGCAACATTATTAA	50862
rs760475691	snp	A/G	0.000164894	0.00907854	synonymous-codon	RNF141	GRCh38.p7	11:10530649	CAGTCTCACCTTGGT[A/G]CAGACCACCCGTACA	50862
rs760477215	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10526839	TTTTAGAACCATCTC[C/T]AATAATCAGAAAGTT	50862
rs760572581	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513464	CCTTGTTTTATTACA[C/T]GCCGAAATGTTAATG	50862
rs760600347	snp	G/T	1.65715e-05	0.00287845	intron-variant	RNF141	GRCh38.p7	11:10530761	GCCGTTCTGAAAAGA[G/T]ACAAGAACATGTTAA	50862
rs760664174	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10527858	GGTGGTAGTAGCGTA[C/G]ATGGTGAGAGCTAGC	50862
rs760786135	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10530005	ATGAATGCCCAATTT[A/C]TGGTTTATATGCATA	50862
rs760805319	snp	C/G	1.65403e-05	0.00287574	missense	RNF141	GRCh38.p7	11:10515064	TTCCTGTGTCGATCA[C/G]TCCTATTAGAGAAGT	50862
rs760812378	snp	C/G	4.97971e-05	0.0049896	synonymous-codon	RNF141	GRCh38.p7	11:10514934	TGGCCTGTGGGGCTG[C/G]CCTGCCTCATCAGCC	50862
rs760837692	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10530408	TAGTATGATGTAATG[A/G]TTAGAGATATTGAGG	50862
rs760955518	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10517176	ATAGTAAGAAGAGAC[A/G]TGAAAGATAATAAAA	50862
rs761011589	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541718	AATGATAGATATGAT[A/G]ATGAGCACATGTTAG	50862
rs761053543	snp	A/G	1.64961e-05	0.00287189	missense	RNF141	GRCh38.p7	11:10534145	TGTGTCTGATCCGAA[A/G]TTTGCTGTCCCATGA	50862
rs761064668	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542445	ATAAATTCCAAAAGA[C/T]ATCAAATTCAACAAG	50862
rs761066689	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529728	CAAAATCTGTGATAA[C/T]CTGGATCAGAAGAGA	50862
rs761072360	snp	A/G	1.64871e-05	0.00287111	synonymous-codon	RNF141	GRCh38.p7	11:10525317	TTTATAAAGTTGAAT[A/G]AACTGGTATAAATTC	50862
rs761137326	in-del	-/AT			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514096	ATTTAGAAATATAAA[-/AT]TTAGTATTTGTGATG	50862
rs761313840	in-del	-/GTC			intron-variant	RNF141	GRCh38.p7	11:10527465	CAAAGGCTGTTTAAT[-/GTC]AGAGGTGTACCTGGC	50862
rs761413466	snp	A/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10511947	ATCACTTGCGAAAGA[A/T]TATTTATTGCACAAT	50862
rs761460975	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533453	ATTAGAAAATATGAA[C/T]AAATGAAATATATTA	50862
rs761462415	in-del	-/C	1.74961e-05	0.00295766	intron-variant	RNF141	GRCh38.p7	11:10519178	AAACAATTATATTCT[-/C]CTGTCATTATGCTTT	50862
rs761475888	snp	A/T	1.66059e-05	0.00288144	intron-variant	RNF141	GRCh38.p7	11:10530764	GTTCTGAAAAGAGAC[A/T]AGAACATGTTAATTT	50862
rs761552426	snp	A/G	1.65751e-05	0.00287876	missense	RNF141	GRCh38.p7	11:10525205	ACCTTCCCATCCAAA[A/G]ACTAGCCTGACAAGA	50862
rs761604128	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10520793	TAGGATGGCTACGAC[A/G]TCCACAGGCAATAGG	50862
rs761659986	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10538612	TGGTCTGTCTTCTGG[C/G]AGATACACAAGCACT	50862
rs761684253	snp	A/G	3.30524e-05	0.00406511	missense	RNF141	GRCh38.p7	11:10534016	AAGAGCAAGCCTTAC[A/G]CATCATTAAGCTCAG	50862
rs761715271	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10526579	ATGAGGTCAGGAGAT[G/T]GAGACCATCCTGGCT	50862
rs761758722	in-del	-/TAAAA			intron-variant	RNF141	GRCh38.p7	11:10525848	GCAAGAAAATTACTT[-/TAAAA]TAAATCCTAACAAAA	50862
rs761846294	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10530153	TGAATCTACTCAGTG[C/G]TGGTTGAGGCTTTCT	50862
rs761905082	snp	G/T	4.98368e-05	0.00499158	intron-variant	RNF141	GRCh38.p7	11:10515079	CTCCTATTAGAGAAG[G/T]CAAAACAAAACAGTT	50862
rs762043088	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10515561	AAAAATTCCTTCTGA[A/G]TCCCAAGAGGAAATT	50862
rs762195869	snp	A/G	1.64933e-05	0.00287165	missense	RNF141	GRCh38.p7	11:10514971	AGAATATAGTTAGCC[A/G]TATCATCTTCAGTGG	50862
rs762253712	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10531521	TTGAAAATTTTTGTT[C/T]AGATAATTTGGGGCT	50862
rs762349256	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10519369	AAAGACTAGATAAAA[-/G]ATACATTTTGTGATA	50862
rs762357896	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10534236	AAAAGTTACTTTTAC[A/G]TATTATACAAAAACG	50862
rs762441184	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542706	GCAAGATACAAAATC[A/T]AATATACAAAAATCA	50862
rs762457068	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10526782	GCAAGACTACGTCTC[-/A]AAAAAAAAAAAAAAG	50862
rs762568542	snp	A/G	3.30606e-05	0.00406561	missense	RNF141	GRCh38.p7	11:10525340	ATAAATTCATGATCC[A/G]TGATGCCTCCACAAT	50862
rs762643877	in-del	-/G			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10539315	AAAATGGAAAAGGCT[-/G]AAAATGCACCAAAAT	50862
rs762666979	snp	A/G	1.65272e-05	0.0028746	intron-variant	RNF141	GRCh38.p7	11:10530622	CTTAAGCTCAGAGGT[A/G]GAAGTCTCCATCAGT	50862
rs762759302	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517010	GAACTACCAGACATA[C/T]AAAAAAGCAGCAGAA	50862
rs762792507	snp	G/T	1.64773e-05	0.00287026	missense	RNF141	GRCh38.p7	11:10534116	CTTTTTCTGGTAACT[G/T]GTTAATAACCAACTG	50862
rs763008535	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513467	TGTTTTATTACATGC[C/T]GAAATGTTAATGTTA	50862
rs763084457	snp	A/C			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540798	GGCCGAATGACTGAG[A/C]CGGCGGCAATATTCA	50862
rs763285524	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519831	GGAAGTTGCTCTAGG[C/T]GAGTCAGTGAGTGAG	50862
rs763324145	snp	G/T	1.66932e-05	0.002889	intron-variant	RNF141	GRCh38.p7	11:10515096	AAAACAAAACAGTTT[G/T]CTTTCTTCTTTTTTA	50862
rs763378380	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10533296	CATAGCTTCTACATA[G/T]ATCAATACCAAAATT	50862
rs763442409	snp	C/T	1.65116e-05	0.00287324	missense	RNF141	GRCh38.p7	11:10519109	CCATCCATACAGATA[C/T]AACACTCCTCCTCAT	50862
rs763467997	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10531867	AATAATTCAGCCGTG[C/T]CAGTTTCCAGCTCTG	50862
rs763700921	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519478	ATAAACAAATTTAAC[C/T]GATATAGTTATTGCA	50862
rs763723881	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542707	CAAGATACAAAATCA[A/T]ATATACAAAAATCAG	50862
rs763860901	snp	C/T	1.64901e-05	0.00287137	missense	RNF141	GRCh38.p7	11:10530650	AGTCTCACCTTGGTA[C/T]AGACCACCCGTACAA	50862
rs763890350	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10543043	ATTGTCCTAAGCAAA[A/G]TAATGCAGAAACAGG	50862
rs763916084	snp	A/C/T	4.97899e-05	0.00498928	intron-variant	RNF141	GRCh38.p7	11:10530763	CGTTCTGAAAAGAGA[A/C/T]AAGAACATGTTAATT	50862
rs763986163	in-del	-/ACACACAC			intron-variant	RNF141	GRCh38.p7	11:10532497	TTTAGTTCATTTTCT[-/ACACACAC]ACACACACACACACA	50862
rs764068847	snp	A/C/G	6.6275e-05	0.00575619	missense	RNF141	GRCh38.p7	11:10514938	CTGTGGGGCTGGCCT[A/C/G]CCTCATCAGCCATGT	50862
rs764154377	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10536155	ACTTGACCTAGTTTT[C/G]TATCAGGGAAGAAGT	50862
rs764218490	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10537569	TCCAGCTGGGCCCAA[G/T]AATTAAACTAACCTA	50862
rs764219853	in-del	-/ACTG			intron-variant	RNF141	GRCh38.p7	11:10521470	TGTAATAATATAAAA[-/ACTG]ACTGTTCCAAAGTAC	50862
rs764281779	snp	A/G			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540803	AATGACTGAGCCGGC[A/G]GCAATATTCAAACAA	50862
rs764295103	snp	C/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513866	ATTTTAGTAGAGAGA[C/G]GATTTCGCCATGTTG	50862
rs764378039	in-del	-/TCCGAAATTTGCTG	1.64874e-05	0.00287113	frameshift-variant	RNF141	GRCh38.p7	11:10534139	ACCAACTGTGTCTGA[-/TCCGAAATTTGCTG]TCCCATGATGAAAAG	50862
rs764499847	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10519857	GTGAGTAGTGGTGAG[A/T]GGATATGAAGGCCTA	50862
rs764567589	snp	A/T	6.6119e-05	0.00574936	utr-variant-5-prime	RNF141	GRCh38.p7	11:10534160	ATTTGCTGTCCCATG[A/T]TGAAAAGATGTCTTT	50862
rs764630039	in-del	-/CAC			intron-variant	RNF141	GRCh38.p7	11:10532541	CACACACACACACCC[-/CAC]AACTATATACAGCTT	50862
rs764657761	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542904	AGACATGGAATCAAC[C/T]CAGGTGCTTATCAAT	50862
rs764754688	snp	G/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541845	GCTCTTGTTTAAGTC[G/T]TCTGGTCAAAGTTGC	50862
rs764816495	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10522539	GAGAAAAGACCATCT[-/G]GGAAAGCCTCCAGTA	50862
rs764826272	snp	G/T	4.9703e-05	0.00498488	missense	RNF141	GRCh38.p7	11:10519131	CCTCCTCATCGGTCA[G/T]CTGCTTCACCCTGCA	50862
rs764929213	snp	C/T	1.6522e-05	0.00287414	missense	RNF141	GRCh38.p7	11:10534017	AGAGCAAGCCTTACA[C/T]ATCATTAAGCTCAGC	50862
rs764957940	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10521659	TAAGTGCTAAGTAAA[A/G]AAGGAAGAGATGAAT	50862
rs764978519	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10534710	GCTAGGTGATTTATC[G/T]AAAGTTACACAGCTG	50862
rs765103325	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542703	GTTGCAAGATACAAA[A/T]TCAAATATACAAAAA	50862
rs765200826	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10515403	GTTTATTCTTTTTAA[A/C]ATACACTGTATCGCT	50862
rs765265827	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519179	AAACAATTATATTCT[C/T]TGTCATTATGCTTTA	50862
rs765364227	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10525574	CAAACTTCTTATACA[A/C]ATTTACCTCATTTAA	50862
rs765366083	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10538871	ACAAGATACTCCCCC[A/C]TAGGCCATGCAACAG	50862
rs765416899	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10526840	TTTAGAACCATCTCT[A/G]ATAATCAGAAAGTTG	50862
rs765493420	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10515883	GTAATTTTTCTGGCA[-/G]GGGAAGAACTCATAT	50862
rs765551269	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10517309	AAAGAGATAGCAATA[A/G]TAACTATCCAGGATG	50862
rs765603963	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537631	TTTATTTAGTAATTT[C/T]TATACATACACAGGA	50862
rs765614627	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10518438	ATTGATACATGCTAC[A/C]ACATGAATAAATACC	50862
rs765639255	snp	C/G	1.64885e-05	0.00287123	missense	RNF141	GRCh38.p7	11:10514981	TAGCCATATCATCTT[C/G]AGTGGGTGCATCTGA	50862
rs765730009	in-del	-/AAAAAA			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542788	ATATCTCTTATCAGC[-/AAAAAA]AAAAAAAAAAAAAAA	50862
rs765767924	snp	A/G	1.66269e-05	0.00288326	intron-variant	RNF141	GRCh38.p7	11:10515081	CCTATTAGAGAAGTC[A/G]AAACAAAACAGTTTG	50862
rs765809642	in-del	-/GAAAAAC	1.67866e-05	0.00289707	intron-variant	RNF141	GRCh38.p7	11:10533984	TACATACAACAAGGG[-/GAAAAAC]GAAAAACAAAAAGAG	50862
rs765877377	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10521399	TTTTAATTTCTTTTA[A/G]CCTTTGTGCTTTTTT	50862
rs765901793	snp	C/G	1.65877e-05	0.00287986	missense	RNF141	GRCh38.p7	11:10525349	TGATCCGTGATGCCT[C/G]CACAATGCCACTGCT	50862
rs765965313	in-del	-/AC			intron-variant	RNF141	GRCh38.p7	11:10533573	TGTGTGTGTCTATAT[-/AC]ACACACACATGAATG	50862
rs765986063	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10527518	AGAAGCCCAGAGTGT[C/T]TGGAACAGAGTGACA	50862
rs766255440	in-del	-/ATAGAC			intron-variant	RNF141	GRCh38.p7	11:10522762	TGACAGTTAACTCTT[-/ATAGAC]AAATTATTATGTGTC	50862
rs766402007	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512284	GATTAGTTATTACAG[C/T]AGAACTGACCTAACA	50862
rs766407205	in-del	-/AATG			intron-variant	RNF141	GRCh38.p7	11:10530260	ATCTTTTTTCTTTTT[-/AATG]AATGAATGTATTCTT	50862
rs766411439	snp	A/C			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540901	CACCGCCACCCCGGG[A/C]AACTGGAACCCGCCG	50862
rs766481797	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537489	ATTTAATATAAATAC[C/T]TATGATAATTTAACC	50862
rs766565764	snp	C/T	0.000189268	0.00972617	intron-variant	RNF141	GRCh38.p7	11:10531971	GCCAATTCTGACCCA[C/T]GGAAATTGGTTTTAA	50862
rs766573350	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517184	AAGAGACATGAAAGA[C/T]AATAAAAACCCAAAT	50862
rs766689196	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529800	CATATATTCCTAATG[C/T]CTCTCACACTTGTGC	50862
rs766691226	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542714	CAAAATCAAATATAC[A/T]AAAATCAGTTGTATT	50862
rs766719823	snp	G/T	0.000167182	0.00914129	intron-variant	RNF141	GRCh38.p7	11:10515099	ACAAAACAGTTTGCT[G/T]TCTTCTTTTTTAAAA	50862
rs766724846	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542461	ATCAAATTCAACAAG[A/G]TTCCATAGTTCAGCC	50862
rs766739975	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10530448	ATTTGATTATAAAAA[C/T]CCCTGCTGTATAGCA	50862
rs766755550	in-del	-/AT			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514414	TAACCACAAGGGGGC[-/AT]ATATATATATACTCC	50862
rs766778103	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10516086	GCTCTTTGGCTTTTA[C/T]GCAAAAATTTAGAAC	50862
rs766864759	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541134	CACCCCAGGTTCAAG[G/T]CATCGCGCACCCTGC	50862
rs767014139	in-del	-/CATT	0.000302821	0.0123012	intron-variant	RNF141	GRCh38.p7	11:10525182	AATACAATACTTATG[-/CATT]ATATACCTTCCCATC	50862
rs767061275	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10524669	TAATGTATTAGGCCT[A/G]GGTAAACAAACATCA	50862
rs767147454	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519938	GTCTTTCTTGGGCCA[C/T]ATATATACTAACACT	50862
rs767152890	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10522763	GACAGTTAACTCTTA[C/T]AGACAAATTATTATG	50862
rs767261016	snp	A/G	1.68695e-05	0.00290422	synonymous-codon	RNF141	GRCh38.p7	11:10525368	AATGCCACTGCTTTT[A/G]TTAATCTAAAAATAC	50862
rs767267473	snp	G/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511217	CAGGCCGCACAGCAG[G/T]AGTTGAGCCGCGGGC	50862
rs767320811	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10511996	AATAACACAGATCCT[A/G]TTATTCTCAACCTCT	50862
rs767463266	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10515605	GGAAGATTTGGTCAA[A/C]GTGTCAAGTATAAAT	50862
rs767662251	snp	A/C			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541502	GCTGGCGACCAAGGC[A/C]GCACTGAGAGCCCTG	50862
rs767802163	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10514534	GATGGCTACAACTTT[C/T]TAATATTCGAGGTTT	50862
rs768135166	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10529931	CCGTGACTCAAAGGA[A/G]AAATCTCCTAACCCA	50862
rs768139312	snp	A/G	4.94376e-05	0.00497156	synonymous-codon	RNF141	GRCh38.p7	11:10534054	CCCAAGAAATTCTTC[A/G]TAAGTTAAGGAGCCA	50862
rs768204939	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10520989	GATAATGGGCATATG[A/C]GTGAAAGAATAGTTT	50862
rs768359176	in-del	-/TTCT	6.69176e-05	0.00578397	intron-variant	RNF141	GRCh38.p7	11:10515102	AAACAGTTTGCTTTC[-/TTCT]TTTTTAAAAACAGGA	50862
rs768364112	snp	C/G			downstream-variant-500B	RNF141	GRCh38.p7	11:10511314	CATGAACTCTACTGT[C/G]AACTGCGCATACGAG	50862
rs768393810	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10526919	GTTCTTTGTACTAAA[A/G]GACTGTACATGAGGT	50862
rs768454057	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10533730	TATTGGTATAAAATT[A/G]AGATGCTGGGATGTA	50862
rs768704564	in-del	-/T			intron-variant	RNF141	GRCh38.p7	11:10525141	ATTAATAGATTTCAG[-/T]TGTTTTCATATTAGA	50862
rs768782156	in-del	-/T			intron-variant	RNF141	GRCh38.p7	11:10530441	AAAAGAATTTGATTA[-/T]TAAAAACCCCTGCTG	50862
rs768784099	snp	C/T	4.95021e-05	0.0049748	missense	RNF141	GRCh38.p7	11:10519091	AGGATGAGGTCAGCC[C/T]GCCCATCCATACAGA	50862
rs768804070	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529477	TAACAATGATACAGT[C/T]TTAAGTTAGTTAAGC	50862
rs768832520	snp	C/T			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540396	AATAACAATCGTAAA[C/T]CCACATTTTGTAACG	50862
rs769087254	snp	C/T	3.31e-05	0.00406803	intron-variant	RNF141	GRCh38.p7	11:10530613	CCAAAATAGCTTAAG[C/T]TCAGAGGTAGAAGTC	50862
rs769504529	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10536956	TAAAGGATACTAATA[A/C]ATTAGAACATATTCA	50862
rs769602983	snp	A/G	1.64893e-05	0.0028713	stop-gained	RNF141	GRCh38.p7	11:10525322	AAAGTTGAATAAACT[A/G]GTATAAATTCATGAT	50862
rs769682932	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10521169	CCTTTGCAGATGGTA[C/T]TTTCCTTTCCTGAAA	50862
rs769852485	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10520478	CACTGGAAGGTCTTC[A/G]GGGGCAGTAACATGC	50862
rs769931696	snp	C/G	3.63174e-05	0.00426115	intron-variant	RNF141	GRCh38.p7	11:10519189	ATTCTCTGTCATTAT[C/G]CTTTATACTTTTTGT	50862
rs769940287	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519514	GACAGAGATACGGTC[C/T]GAGAAACTCATTGTT	50862
rs769942664	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10524137	AAGAAACCACTGGCC[A/G]GGCATGGTGGCTCAT	50862
rs770077979	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10533149	GATGTGGATGTTGCT[A/T]GAGGCAGATTTAAAA	50862
rs770135379	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513297	TGAATTTTATTTGCT[C/T]GCCTATTAAAATCCT	50862
rs770204177	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10516428	CTCGAGAGTTTCTAG[C/T]CCCTGATCAAGAAGC	50862
rs770222771	snp	C/T			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10539689	TCAGAAAAAGATACA[C/T]ACATATATATTAGAG	50862
rs770366432	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10523171	CAAAGTGTTATCTGA[C/G]GATCAGCAGCATTGG	50862
rs770391015	snp	C/T	1.65168e-05	0.00287369	intron-variant	RNF141	GRCh38.p7	11:10530629	TCAGAGGTAGAAGTC[C/T]CCATCAGTCTCACCT	50862
rs770497717	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10536779	GTCTGGGGTTTTTAA[C/T]CAAAATAAGTCAACA	50862
rs770636407	snp	A/C	4.94858e-05	0.00497398	missense	RNF141	GRCh38.p7	11:10530732	GATGTTTTTCCTGGC[A/C]AGAAGCCACTTTAGC	50862
rs770748407	snp	A/C	1.65064e-05	0.00287279	missense	RNF141	GRCh38.p7	11:10515051	ACAAATAGGGCAATT[A/C]CTGTGTCGATCACTC	50862
rs770795843	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10515370	ACAGACTAGTATGTA[C/T]CAGCACCTGTTAGAG	50862
rs770824436	snp	A/G	1.68052e-05	0.00289867	stop-lost	RNF141	GRCh38.p7	11:10514918	TTTCACTTCAAGGTC[A/G]TGGCCTGTGGGGCTG	50862
rs770831081	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10529220	CTCTGTCAGTGTAGG[C/T]GTATGAAGGGGATAT	50862
rs770924583	in-del	-/CTGCACCTTTCAGTTCTTA			intron-variant	RNF141	GRCh38.p7	11:10527462	ATACAAAGGCTGTTT[-/CTGCACCTTTCAGTTCTTA]AATAGAGGTGTACCT	50862
rs770973074	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10532858	CTGCTAGTCGATTTC[A/T]TTCAGCCTTTTTAGG	50862
rs771027764	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10519349	GAGGGCTACATTTCA[C/T]AAAGAAAGACTAGAT	50862
rs771027950	in-del	-/CCACA			intron-variant	RNF141	GRCh38.p7	11:10532540	ACACACACACACACC[-/CCACA]ACTATATACAGCTTT	50862
rs771060393	snp	A/G			upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541482	AGCGGAAAGTGGAGC[A/G]CCCCGCTGGCGACCA	50862
rs771131907	in-del	-/ACACACC			intron-variant	RNF141	GRCh38.p7	11:10532533	CACACACACACACAC[-/ACACACC]CCACAACTATATACA	50862
rs771208043	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10531482	GGTTCAGTCCTTGTT[C/T]AAACAATGATACTAA	50862
rs771292597	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512371	TTTATTTATTTGATA[A/G]GGCTAATAACATTTT	50862
rs771305588	snp	A/G	1.64776e-05	0.00287028	synonymous-codon	RNF141	GRCh38.p7	11:10534117	TTTTTCTGGTAACTT[A/G]TTAATAACCAACTGT	50862
rs771464946	snp	C/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511501	CTACAGCAGGGTGAA[C/T]AGACATACGAACAAA	50862
rs771510261	snp	A/G	3.30267e-05	0.00406353	missense	RNF141	GRCh38.p7	11:10530749	GAAGCCACTTTAGCC[A/G]TTCTGAAAAGAGACA	50862
rs771517136	in-del	-/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513553	TCCATTATTACTATA[-/T]TGTTTCAGAATATTT	50862
rs771576910	snp	C/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512445	AAATAAAAAGGTTTG[C/G]GCCCTATTGAGTCAC	50862
rs771593211	in-del	-/AT			intron-variant	RNF141	GRCh38.p7	11:10519264	AGCACAATATGACTC[-/AT]GTGCAAAATCAGACT	50862
rs771635089	snp	A/G	1.66125e-05	0.00288201	intron-variant	RNF141	GRCh38.p7	11:10534003	AACGAAAAACAAAAA[A/G]AGCAAGCCTTACACA	50862
rs771920104	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10527799	AGATCAGTTAGGAGG[C/G]TACTGGAATAATCCT	50862
rs771924663	snp	A/G	9.91391e-05	0.00703987	stop-gained	RNF141	GRCh38.p7	11:10515059	GGCAATTCCTGTGTC[A/G]ATCACTCCTATTAGA	50862
rs771958373	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10538664	ATGCAGTAAATACCA[C/T]TGGCAGTTTTTGTTT	50862
rs772025491	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10527439	CATTCCAGGCTGAGA[C/T]AACAGGAAATACAAA	50862
rs772049460	snp	C/T	1.65165e-05	0.00287367	missense	RNF141	GRCh38.p7	11:10519052	TTATCAATACACTTC[C/T]GACAAAAGCTGTGAG	50862
rs772159226	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10530167	GGTGGTTGAGGCTTT[C/T]TAATACTCAATGACA	50862
rs772205862	snp	G/T			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540683	GGTGTCCAGCCCGGC[G/T]GAGACCGAGCCCGCG	50862
rs772216421	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10517032	GCAGCAGAAAAATAT[A/C]ATCTATAATAAAGAG	50862
rs772219620	in-del	-/ACCCCA			intron-variant	RNF141	GRCh38.p7	11:10532537	CACACACACACACAC[-/ACCCCA]CAACTATATACAGCT	50862
rs772249549	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10518674	CTGATCTCTAAAGTT[A/C]CCTGAGGTCCAGTAT	50862
rs772336104	snp	A/C			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542306	AGCGCTAGGTCCATG[A/C]CTGTTTGTGCACCAT	50862
rs772444952	snp	A/G	1.6669e-05	0.00288691	missense	RNF141	GRCh38.p7	11:10514927	AAGGTCATGGCCTGT[A/G]GGGCTGGCCTGCCTC	50862
rs772538609	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10522966	GCTAGAGTCTGTGCC[C/G]TGCTGCCTCAAGAAA	50862
rs772591833	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10524186	CTGGGAGGCCGAGGA[A/G]GGCAGGATCATGAGG	50862
rs772612186	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10531655	AATGTATCACTTCTA[A/G]AAGATAATTCAATAT	50862
rs772657457	snp	A/C	1.65455e-05	0.00287619	intron-variant	RNF141	GRCh38.p7	11:10530610	CCACCAAAATAGCTT[A/C]AGCTCAGAGGTAGAA	50862
rs772658524	in-del	-/AAG			intron-variant	RNF141	GRCh38.p7	11:10519332	TAGGGAAAAAGTATT[-/AAG]AGGGCTACATTTCAT	50862
rs772732014	snp	A/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513431	TACATGGAATGTTAA[A/G]TTTTAAAGGAGATAG	50862
rs772769394	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10535752	CTGAAAAGTAGGATA[G/T]AATATTAGAAAAAAA	50862
rs772770620	in-del	-/G	1.64887e-05	0.00287125	frameshift-variant	RNF141	GRCh38.p7	11:10525322	AAAGTTGAATAAACT[-/G]GTATAAATTCATGAT	50862
rs772864956	snp	C/T	1.64773e-05	0.00287026	missense	RNF141	GRCh38.p7	11:10534115	ACTTTTTCTGGTAAC[C/T]TGTTAATAACCAACT	50862
rs772963247	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10515357	GTCAATATATCTTAC[A/G]GACTAGTATGTATCA	50862
rs773060088	snp	C/T	1.65261e-05	0.0028745	intron-variant	RNF141	GRCh38.p7	11:10530621	GCTTAAGCTCAGAGG[C/T]AGAAGTCTCCATCAG	50862
rs773218483	snp	A/C/G	5.0614e-05	0.00503039	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514914	AGACTTTCACTTCAA[A/C/G]GTCATGGCCTGTGGG	50862
rs773219043	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10531299	AGCATTGCTTGAACA[C/T]GGGAGGTGAAGGTTG	50862
rs773241796	snp	A/G	1.7093e-05	0.00292339	intron-variant	RNF141	GRCh38.p7	11:10525149	ATTTCAGTTGTTTTC[A/G]TATTAGAAAATAAGT	50862
rs773260260	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10538757	AGGTTGGAGAGAAGC[A/C]GAAGTTAAAAATATG	50862
rs773398747	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10533816	TAAGTTCTTTCCATA[C/T]CTTCTGTCCCCATTA	50862
rs773452894	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10530288	ATTCTTAAAAGAAAT[A/G]ATCTCAAGATAACAT	50862
rs773552610	snp	A/G	1.65179e-05	0.00287379	synonymous-codon	RNF141	GRCh38.p7	11:10534018	GAGCAAGCCTTACAC[A/G]TCATTAAGCTCAGCT	50862
rs773578330	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10535765	TATAATATTAGAAAA[A/C]AAGTCTTTCCCAAGA	50862
rs773630598	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541689	TACAAGGTTCAAAAT[C/T]CTGAGCTTTGATAAA	50862
rs773738293	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10531749	TCATTACTAACAACT[C/G]TCTCTGAGCACCAGT	50862
rs773769453	snp	A/G	1.65061e-05	0.00287277	synonymous-codon	RNF141	GRCh38.p7	11:10519105	CCGCCCATCCATACA[A/G]ATACAACACTCCTCC	50862
rs773800330	snp	A/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513261	CTACCCCTGGCCAGA[A/T]GTTTTTCCTTGAAAT	50862
rs773831776	snp	A/G	0.000366868	0.0135388	missense	RNF141	GRCh38.p7	11:10530734	TGTTTTTCCTGGCCA[A/G]AAGCCACTTTAGCCG	50862
rs773841615	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10521017	TTTAGTCTTAAGTAT[C/T]AGGTGCTGTGAGAGA	50862
rs774000844	in-del	-/CTGAG	1.6941e-05	0.00291036	intron-variant	RNF141	GRCh38.p7	11:10519156	CCTGCAATGTGAAAA[-/CTGAG]CTGAAACAATTATAT	50862
rs774111596	in-del	-/ATGATCTTCCCCCTAGACATCTATATGACTCA			intron-variant	RNF141	GRCh38.p7	11:10527459	GAAATACAAAGGCTG[lengthTooLong]TTTAATAGAGGTGTA	50862
rs774168894	in-del	-/C			intron-variant	RNF141	GRCh38.p7	11:10539144	TGGTACATAGTGAAT[-/C]CACTTATTTTTCTAA	50862
rs774238595	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10529540	GTGACTAATGCAGAA[A/T]AGATAGTTTGGAGTC	50862
rs774252527	snp	A/C	1.67522e-05	0.0028941	missense	RNF141	GRCh38.p7	11:10514922	ACTTCAAGGTCATGG[A/C]CTGTGGGGCTGGCCT	50862
rs774380576	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537085	GAAAAACAAGATTCA[C/T]TTACAGAGAATGGGA	50862
rs774406231	in-del	-/T			intron-variant	RNF141	GRCh38.p7	11:10530141	AACTTTCTATCTGAA[-/T]TCTACTCAGTGGTGG	50862
rs774526642	snp	G/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513985	TGGCCTCTTGTCTCT[G/T]AATCTAAGAAATTTG	50862
rs774644948	snp	C/T	1.64803e-05	0.00287052	synonymous-codon	RNF141	GRCh38.p7	11:10534126	TAACTTGTTAATAAC[C/T]AACTGTGTCTGATCC	50862
rs774762726	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10519868	TGAGTGGATATGAAG[A/G]CCTAGGACAGGAGTG	50862
rs774822993	in-del	-/C			intron-variant	RNF141	GRCh38.p7	11:10518055	TGGAGAAATATACAG[-/C]CGTATGTGGATAGGA	50862
rs774867270	snp	C/T			downstream-variant-500B	RNF141	GRCh38.p7	11:10511630	TTTCTTATTCCCGGA[C/T]AGACTAAGCTTGACT	50862
rs774933615	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10526178	TCAGCACAAGACATA[A/G]GATGGAAGACTGGGG	50862
rs774949862	snp	C/G	1.65996e-05	0.00288089	intron-variant	RNF141	GRCh38.p7	11:10534005	CGAAAAACAAAAAGA[C/G]CAAGCCTTACACATC	50862
rs775001801	snp	C/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542705	TGCAAGATACAAAAT[C/T]AAATATACAAAAATC	50862
rs775027051	snp	C/T			utr-variant-5-prime	RNF141	GRCh38.p7	11:10534200	GAGTGTTGCTTCACA[C/T]AGTTTCTGTCAAATA	50862
rs775113625	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10536971	AATTAGAACATATTC[A/G]TGGGCATAGAAAAAA	50862
rs775164323	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10524748	TGCATTCGGTTCCTT[C/T]CTGAATGGACTGCCA	50862
rs775257522	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10532542	ACACACACACACCCC[-/A]CAACTATATACAGCT	50862
rs775261149	in-del	-/AT			intron-variant	RNF141	GRCh38.p7	11:10521532	TAGGAGCTATCACTA[-/AT]ATGTTTTCCATTCCC	50862
rs775463310	snp	G/T	1.65531e-05	0.00287686	intron-variant	RNF141	GRCh38.p7	11:10530759	TAGCCGTTCTGAAAA[G/T]AGACAAGAACATGTT	50862
rs775494838	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10530066	GGGTGGGGATAGGAG[A/G]TGGCCTAATAAAATT	50862
rs775515281	in-del	-/GA			intron-variant	RNF141	GRCh38.p7	11:10531508	ACTAACAAACCTCTT[-/GA]AAATTTTTGTTCAGA	50862
rs775646881	snp	C/T			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540661	CAGGCAAAAGGTTTC[C/T]TATTTGGGTGTCCAG	50862
rs775814571	snp	C/G	1.66056e-05	0.00288141	missense	RNF141	GRCh38.p7	11:10514933	ATGGCCTGTGGGGCT[C/G]GCCTGCCTCATCAGC	50862
rs775822927	in-del	-/AGTAT			intron-variant	RNF141	GRCh38.p7	11:10520618	CTAAAATGATTAAAA[-/AGTAT]AGTATAGTATAATAA	50862
rs775867465	snp	A/G	1.65353e-05	0.00287531	synonymous-codon	RNF141	GRCh38.p7	11:10515063	ATTCCTGTGTCGATC[A/G]CTCCTATTAGAGAAG	50862
rs775893797	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10531845	AGGAAACAAAGTCTT[C/T]GGTGAAAATAATTCA	50862
rs775901670	snp	A/G	1.64849e-05	0.00287092	stop-gained	RNF141	GRCh38.p7	11:10525313	TATCTTTATAAAGTT[A/G]AATAAACTGGTATAA	50862
rs775948716	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10536801	AAGTCAACAGTATAA[C/T]GGGGGCAACAAGTAT	50862
rs776152653	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10523294	CCATAAAGTAATAGG[C/T]TAGAGCACAGCTGTA	50862
rs776204779	snp	A/G	1.65883e-05	0.00287991	missense	RNF141	GRCh38.p7	11:10525202	TATACCTTCCCATCC[A/G]AAGACTAGCCTGACA	50862
rs776318413	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10529467	AAAAGAAAAGTAACA[A/G]TGATACAGTCTTAAG	50862
rs776379196	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10535823	CCACATATTTACCAG[A/G]TATACTACACATTGT	50862
rs776551148	snp	C/T	1.6571e-05	0.0028784	intron-variant	RNF141	GRCh38.p7	11:10515071	GTCGATCACTCCTAT[C/T]AGAGAAGTCAAAACA	50862
rs776646363	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10519361	TCATAAAGAAAGACT[A/G]GATAAAAGATACATT	50862
rs776674277	snp	A/C/G			utr-variant-3-prime	RNF141	GRCh38.p7	11:10513862	TTGTATTTTAGTAGA[A/C/G]AGAGGATTTCGCCAT	50862
rs776818350	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10531574	TGAGACACTTTATAT[A/G]TAGCTCTACTGTCCT	50862
rs776880104	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10532944	ATGCCATTAATACCT[A/G]CGTAATCAACTTGGC	50862
rs777002999	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10524441	AAGTACATTCTTAAC[C/T]TTAAGGTAAAGGACA	50862
rs777025393	snp	A/C			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542683	TCATAAGTGAGTTTA[A/C]AAAAGTTGCAAGATA	50862
rs777064860	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10520805	GACGTCCACAGGCAA[C/T]AGGAATTTTTTAGCT	50862
rs777111531	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10516450	TCAAGAAGCGGGAAG[C/T]TTGATGGAACATGGC	50862
rs777259590	snp	C/T	1.64898e-05	0.00287135	synonymous-codon	RNF141	GRCh38.p7	11:10534036	ATTAAGCTCAGCTAC[C/T]CTCCCAAGAAATTCT	50862
rs777280960	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10518068	CAGCGTATGTGGATA[C/G]GAAGATGCACTAGTA	50862
rs777359502	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517523	AAGAAGCTCAATAAA[C/T]CCCAAGCACAAGAAA	50862
rs777483498	in-del	-/AAATG			intron-variant	RNF141	GRCh38.p7	11:10524026	TAATTGGGAAATAAT[-/AAATG]GAAAATACAGTTTAA	50862
rs777668653	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10530837	TAGATTCAAGAAACA[A/G]TTTCAGAGAAGGAAA	50862
rs777750070	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10521910	ATATTAAGTTTGAAC[A/G]TGTCCTGACAAGCAA	50862
rs777831609	in-del	-/ACACA			intron-variant	RNF141	GRCh38.p7	11:10532531	CACACACACACACAC[-/ACACA]CACCCCACAACTATA	50862
rs777865641	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10520165	ACATTTAGGCTATAC[A/G]AAATTTATAAAAAAT	50862
rs777920406	snp	C/T	1.64773e-05	0.00287026	synonymous-codon	RNF141	GRCh38.p7	11:10525287	CAATACTCCTGCTGC[C/T]TGACTTGTGATATCT	50862
rs777928402	in-del	-/AG			intron-variant	RNF141	GRCh38.p7	11:10536989	GGCATAGAAAAAAAA[-/AG]AGGTTTATTCTAGAT	50862
rs777947770	in-del	-/G			intron-variant	RNF141	GRCh38.p7	11:10537782	GTTAATCACAGAAAA[-/G]TGACTAGGAAGATAA	50862
rs777972695	snp	C/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512632	AATCTAAAAGGACAA[C/T]TTAAAATCTTAGAGC	50862
rs777973384	snp	A/G	1.8242e-05	0.00302005	intron-variant	RNF141	GRCh38.p7	11:10525399	AAAGAACATGAAAAA[A/G]AAAAGTTGATCATTT	50862
rs777994280	snp	C/T	1.64784e-05	0.00287035	missense	RNF141	GRCh38.p7	11:10534070	TAAGTTAAGGAGCCA[C/T]TCTCTCGAACCAACG	50862
rs777997279	in-del	-/CC/GACA			intron-variant	RNF141	GRCh38.p7	11:10532537	ACACACACACACACA[-/CC/GACA]CCCCACAACTATATA	50862
rs778152342	in-del	-/T			intron-variant	RNF141	GRCh38.p7	11:10523349	TCTTGGCTAGAACAA[-/T]TTCTAATCATGACAC	50862
rs778202498	snp	A/G			downstream-variant-500B	RNF141	GRCh38.p7	11:10511402	GAAAAATTTCATCCC[A/G]AAACTATTCCCACCC	50862
rs778233977	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10528965	AGAGACAAGAGAACT[C/T]CTATTCAGGAAGACT	50862
rs778290141	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10525917	CTTTATCAAAAAACT[C/T]GTTTAATATGAGGTG	50862
rs778469244	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10541216	ACTCAGGCCGGGACC[C/T]GGTCGCACCTCTGTG	50862
rs778610696	snp	A/C			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540237	TCGTGCTGAAGATGT[A/C]AGAATTATAAACAAT	50862
rs778727093	snp	A/G					GRCh38.p7	11:10520181	AAATTTATAAAAAAT[A/G]TATTTCTTCAATGAT	50862
rs778732576	in-del	-/ACTT					GRCh38.p7	11:10523363	ATTTCTAATCATGAC[-/ACTT]ACTTAGCTAAATCTC	50862
rs778761296	snp	A/G			synonymous-codon	RNF141	GRCh38.p7	11:10519126	ACACTCCTCCTCATC[A/G]GTCAGCTGCTTCACC	50862
rs778779402	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10515415	TAACATACACTGTAT[C/T]GCTATGCCATAATTT	50862
rs778816314	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10532692	ATAAAGACAGTATAT[C/G]AAGCTTATCTAATAT	50862
rs778869236	snp	G/T			intron-variant	RNF141	GRCh38.p7	11:10533834	TCTGTCCCCATTACA[G/T]ACTTTTAAAAAGCTA	50862
rs778944428	snp	G/T	1.65105e-05	0.00287315	missense	RNF141	GRCh38.p7	11:10515054	AATAGGGCAATTCCT[G/T]TGTCGATCACTCCTA	50862
rs778999368	snp	A/T	1.67416e-05	0.00289318	intron-variant	RNF141	GRCh38.p7	11:10519017	GGCCCAGCCCATGAA[A/T]GCAGTAGGTAACTTA	50862
rs779046078	snp	C/T	1.65677e-05	0.00287812	intron-variant	RNF141	GRCh38.p7	11:10530598	ATATAGTTCTAGCCA[C/T]CAAAATAGCTTAAGC	50862
rs779142389	snp	A/G	3.46063e-05	0.00415956	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514879	CATGACCAAATATTT[A/G]AGCCCACAATAGCAA	50862
rs779269391	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10536450	CTGCGGATGACCAAA[A/G]CTGGAATAAATGAAT	50862
rs779293215	snp	A/T			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542718	ATCAAATATACAAAA[A/T]TCAGTTGTATTTCTA	50862
rs779449902	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10516390	CAAAGAAGGTGAGAC[C/T]TATACTTGCCTCAGC	50862
rs779545955	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10527586	TGGGAATAGAATATA[C/T]AGGACTTTGCTGATT	50862
rs779719964	in-del	-/AC			intron-variant	RNF141	GRCh38.p7	11:10532504	ATTTTCTACACACAC[-/AC]ACACACACACACACA	50862
rs779724338	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10538447	CAGAGTGCATGTTCA[C/T]GAAAACAATCTGTTG	50862
rs779845973	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10532379	AACCAATGACTATAT[A/T]TTTATCATAAAAATA	50862
rs779943649	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517935	AAATTTTAAATACCA[C/T]TTAAAATAGCATAAA	50862
rs779993060	snp	A/G	3.44471e-05	0.00414999	intron-variant	RNF141	GRCh38.p7	11:10519168	AAACTGAGCTGAAAC[A/G]ATTATATTCTCTGTC	50862
rs779998788	snp	A/G	1.65031e-05	0.00287251	synonymous-codon	RNF141	GRCh38.p7	11:10519066	CTGACAAAAGCTGTG[A/G]GCACAAGGCAGGATG	50862
rs780001594	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10524001	GAAAACCAAGTAATT[A/C]TATTAAAGATAATTG	50862
rs780046284	in-del	-/A			intron-variant	RNF141	GRCh38.p7	11:10518213	GTTAAACACACACAT[-/A]ACCATATGATCTAGC	50862
rs780143950	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10526813	AATGAGTCATATACC[A/G]TACTAAGAAATTTTA	50862
rs780376152	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10535202	TTGCTTTATCATTAA[C/T]CAAAAAATAAAGCTA	50862
rs780517969	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541650	GCCGAGTTGTTAAGC[A/G]TAAGAGAATGTATGA	50862
rs780587084	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10528630	CTCTTCAATGTGAGC[C/T]GAGTACTTTATGAAA	50862
rs780605779	in-del	-/A			intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540020	AAGTCAGGCAATGTG[-/A]AAAGAAAAGGATAAA	50862
rs780659932	in-del	-/AAAAA			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542789	TATCTCTTATCAGCA[-/AAAAA]AAAAAAAAAAAAAAA	50862
rs780667522	snp	A/G	1.65438e-05	0.00287605	intron-variant	RNF141	GRCh38.p7	11:10530611	CACCAAAATAGCTTA[A/G]GCTCAGAGGTAGAAG	50862
rs780722462	snp	A/G	8.23811e-05	0.00641746	synonymous-codon	RNF141	GRCh38.p7	11:10530682	CACTTTCCAAAAAGC[A/G]GAGGAATCAGACCCA	50862
rs780777449	snp	C/T	1.72469e-05	0.00293652	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514886	AAATATTTGAGCCCA[C/T]AATAGCAACAGAAGA	50862
rs780830372	snp	C/T	1.64827e-05	0.00287073	missense	RNF141	GRCh38.p7	11:10515019	CAAGATTCATTTGCT[C/T]CAGTCATCTGTAGGC	50862
rs780836442	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10519876	TATGAAGGCCTAGGA[C/G]AGGAGTGTACAATCT	50862
rs780890596	snp	G/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10511969	TTGCACAATTTATCA[G/T]TGGGTACTAAGAATA	50862
rs780993643	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10543126	ACAGACACAAAGTTG[A/G]GAACAATAAACACTG	50862
rs781035786	snp	A/G			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542202	CCATTAAGGAGCAGA[A/G]CCAGATTCAAACCCA	50862
rs781040500	snp	C/G	1.64784e-05	0.00287035	synonymous-codon	RNF141	GRCh38.p7	11:10525257	ATCAGGTTCTTCAGA[C/G]GTGGAGCTCTGTGCC	50862
rs781139887	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10516780	TCTCTAAAGGGTCTT[A/G]CTATTAGTGGGACAT	50862
rs781258145	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10520401	ATAACACACACATTA[A/G]CCTAGGCCTAAACAG	50862
rs781288643	snp	A/G	1.79213e-05	0.00299338	intron-variant	RNF141	GRCh38.p7	11:10519184	ATTATATTCTCTGTC[A/G]TTATGCTTTATACTT	50862
rs781372069	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10527469	AGGCTGTTTAATAGA[A/G]GTGTACCTGGCAAGG	50862
rs781425424	snp	A/T			utr-variant-3-prime	RNF141	GRCh38.p7	11:10512767	AATTTAATTAAAAAA[A/T]TTTTTTAAAAAAAAC	50862
rs781490220	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10539129	CACATTCTCTAGTGG[A/G]TGGTACATAGTGAAT	50862
rs781670007	snp	A/C	8.24124e-05	0.00641868	stop-gained	RNF141	GRCh38.p7	11:10530708	ACCCAGGTTGTACCT[A/C]AAAGAGAAGATGTTT	50862
rs781749369	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10526080	GCATAATGAAATGAC[C/T]GAGGCCAGTAAGGTG	50862
rs796279718	in-del	-/GAA			intron-variant	RNF141	GRCh38.p7	11:10519667	GCATGTTACTGTATG[-/GAA]CACTGTAGGCTACTG	50862
rs796280341	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10517993	AAAGATATGCAACAC[C/T]GAAAACTAAAAAAAT	50862
rs796387534	snp	A/G			intron-variant	RNF141	GRCh38.p7	11:10516660	CTGAACAATCAATCA[A/G]AGGGCTTTGAGGGGA	50862
rs796484196	in-del	-/ACACACACACACACACACAC			intron-variant	RNF141	GRCh38.p7	11:10532497	TTTAGTTCATTTTCT[-/ACACACACACACACACACAC]ACACACACACACACA	50862
rs796521514	snp	C/G			intron-variant	RNF141	GRCh38.p7	11:10521716	GATAGAAAAACAATA[C/G]GATTTTAATAGAAGA	50862
rs796532656	in-del	-/AAATA			intron-variant	RNF141	GRCh38.p7	11:10515909	CATATATGATCACTT[-/AAATA]AGATTATGTTTTCGA	50862
rs796691004	in-del	-/AA			intron-variant	RNF141	GRCh38.p7	11:10535479	AAAAAAAAAAAAAAA[-/AA]TCCCTGAAGTCAAAT	50862
rs796855735	snp	A/T			intron-variant	RNF141	GRCh38.p7	11:10532209	TACTGCTCATAAGAG[A/T]TGAAAATATAAACAT	50862

Page 1 | 2