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

RNF213

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs8359	snp	C/T	0.227074	0.248947	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394251	ATCTAGTTTCTCTCA[C/T]AATTTCAAAATGTCA	57674
rs1128358	snp	C/G	0.0349115	0.127424	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395224	TTGTACAGAAATATA[C/G]TGGCCTAGCAGAGGC	57674
rs3185057	snp	A/G	0.145533	0.227127	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390047	TTCAAGGTACAAAGC[A/G]GATCTGAGCCCGGAA	57674
rs3193455	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382063	GTTCCGAAGTCAGCC[A/C]CGTAGGTCATTCCCC	57674
rs3923128	snp	A/G	0.0115895	0.0752359	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389123	GGCTGGGTTTCTGGC[A/G]TCTCACCACCTGGTA	57674
rs4073111	snp	C/G	0.490398	0.0686206	intron-variant	RNF213	GRCh38.p7	17:80283792	GGCGGTCCAGAGCCT[C/G]AGGATTCTCCGTCTA	57674
rs4075499	snp	A/G	0.495252	0.0484902	intron-variant	RNF213	GRCh38.p7	17:80327059	CATAGCATATGCAAA[A/G]AGAGAAACAGCCATG	57674
rs4078429	snp	A/G	0.218151	0.247963	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361572	TAGGGAATTGAAGGA[A/G]TAGTCACTGTCTAGA	57674
rs4523980	snp	C/T	0.382279	0.212137	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373864	AAGCACCCACCATCA[C/T]GTCCAGCTAATTTTT	57674
rs4609905	snp	A/G	0.40853	0.193309	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387972	ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA	57674
rs4889843	snp	C/T	0.448066	0.152544	intron-variant	RNF213	GRCh38.p7	17:80325519	AGATCAGGAAACAAA[C/T]GGAGAAGGCAATGCG	57674
rs4889844	snp	A/G	0.465892	0.126058	intron-variant	RNF213	GRCh38.p7	17:80325697	GCCCCCCGCGCCCCA[A/G]GTGTTTTGTGGTCAA	57674
rs4889845	snp	A/G	0.452473	0.146644	intron-variant	RNF213	GRCh38.p7	17:80329760	cacttgagcctggga[A/G]gtcgaggctgcagtg	57674
rs4889846	snp	A/G	0.493718	0.0556925	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355824	ATGGGGGCTTACAGG[A/G]GAAGAAGCGGGGTGA	57674
rs4889847	snp	A/G	0.0550842	0.15655	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372748	AGGCAAGTCTTCTCT[A/G]CCTTGCTTTCCTTTG	57674
rs4889848	snp	C/T	0.347418	0.230239	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380861	AACGCAGACCGGCCA[C/T]GTGCTGGGCAACCCG	57674
rs4889968	snp	A/G	0.275197	0.248727	intron-variant	RNF213	GRCh38.p7	17:80263005	AGGTCCTCCACTGTT[A/G]GGTGGCCAAGCGCCC	57674
rs4890007	snp	G/T	0.179425	0.239831	intron-variant	RNF213	GRCh38.p7	17:80330752	AACCATCTCTTGGCT[G/T]CTGGGGTGAAGAAGG	57674
rs4890008	snp	G/T	0.162581	0.234218	intron-variant	RNF213	GRCh38.p7	17:80331819	TGCTTTCTTTATCAT[G/T]AATATTGGTTAACAA	57674
rs4890009	snp	A/G	0.457173	0.139926	synonymous-codon	RNF213	GRCh38.p7	17:80337708	CTATGTGATCCAGGC[A/G]CCCAAAGGTGGCCAA	57674
rs4890010	snp	A/G	0.498693	0.0255257	intron-variant	RNF213	GRCh38.p7	17:80342379	GAGGTGACCAGGAGA[A/G]TGAGTAGGTAACGGC	57674
rs4890011	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80342754	ATATATTGTATGTAT[A/G]TATATATTATATATA	57674
rs4890012	snp	A/C/G/T	0.49098	0.0668198	synonymous-codon	RNF213	GRCh38.p7	17:80345580	CCGGTGTGGGATCCC[A/C/G/T]GTTATCATCATGGGA	57674
rs4890013	snp	A/G	0.273856	0.248859	intron-variant	RNF213	GRCh38.p7	17:80351225	CAGGGGCTGTTTcct[A/G]taatcctagctactt	57674
rs4890014	snp	C/T	0.494936	0.050064	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361256	ATATCCTAGGCCAGG[C/T]GCAGTGGTTCACAAC	57674
rs4890015	snp	A/G	0.496583	0.0411924	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361400	TGGTGCATGCCTGTA[A/G]TCCCAGCTACTTGGT	57674
rs4890016	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364057	GGCTATTGTGATGCC[A/G]TGTGAGAAATGCTGT	57674
rs4890017	snp	A/G	0.0733688	0.176922	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378606	GGATTATGAGCCACT[A/G]TGCCCAGCCTGATAC	57674
rs4890018	snp	C/T	0.0961445	0.197049	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386201	CACGCCTAGATTCTG[C/T]GAGGAGTTGGAACTC	57674
rs4890019	snp	A/G	0.382085	0.212258	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398190	tttggttttgacctg[A/G]cttggatatcctgat	57674
rs4890020	snp	A/T	0.382473	0.212016	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399034	cattcaatctgtagc[A/T]gcaactgctttgcta	57674
rs5822349	in-del	-/T/TT	0.45866	0.137698	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368433	ATGTAGACGCCAGTG[-/T/TT]TTTTTTTTTTTTTTT	57674
rs5822350	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377438	ACAAAAAAAAAAAAA[-/A]TCAAGGAAAATAGAA	57674
rs5822351	in-del	-/CC	0.0337553	0.125452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389070	TAGAGAGTTGGCCCC[-/CC]GCATGTGGCTTGGGC	57674
rs6420491	snp	A/G	0.0456336	0.143994	intron-variant	RNF213	GRCh38.p7	17:80331236	ctgtgacataaaact[A/G]ctcagctctcagtgt	57674
rs6565662	snp	G/T	0.448452	0.152042	intron-variant	RNF213	GRCh38.p7	17:80276370	ctcccaaagtgctgg[G/T]attacgggcgtgagc	57674
rs6565663	snp	A/G	0.492137	0.0622048	intron-variant	RNF213	GRCh38.p7	17:80285865	TTAGTAGAGATGGGG[A/G]GGATCTCACCATGTT	57674
rs6565664	snp	G/T	0.0923359	0.194016	intron-variant	RNF213	GRCh38.p7	17:80285919	GACCTCCAGTGATCC[G/T]CCTGCCTCGGCCTCC	57674
rs6565666	snp	A/G	0.291266	0.246571	intron-variant	RNF213	GRCh38.p7	17:80319145	ATAGAGCACTGGAGC[A/G]CTGCATCCGAAAGCT	57674
rs6565667	snp	A/C	0.470034	0.11868	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320375	tgttgtttttgagac[A/C]gagtttcactctttt	57674
rs6565668	snp	A/G	0.495135	0.0490805	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320436	tggctcaccgcaacc[A/G]ctgcctcccgggttc	57674
rs6565669	snp	C/T	0.494442	0.0524218	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321945	gggtcatgatggtct[C/T]gatctcttgacctca	57674
rs6565670	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80322152	gcccctcatcccccc[A/C]acccccccttttttt	57674
rs6565671	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80322153	cccctcatccccccc[A/C]ccccccctttttttt	57674
rs6565672	snp	C/T	0.491421	0.0649309	intron-variant	RNF213	GRCh38.p7	17:80322448	gggcatggtggcatg[C/T]gcctgtagtcccagc	57674
rs6565673	snp	A/T	0.0228947	0.104514	intron-variant	RNF213	GRCh38.p7	17:80322587	tctcaaaaaaaaaaa[A/T]tttttttcgtagaga	57674
rs6565674	snp	A/G	0.000113993	0.00754873	missense	RNF213	GRCh38.p7	17:80325138	ACCGCGGACAACTTC[A/G]ATGACATTTTAAAGC	57674
rs6565675	snp	A/G	0.497445	0.0356514	intron-variant	RNF213	GRCh38.p7	17:80326282	ggcgtgcaccaccat[A/G]cccagccTGTTTATA	57674
rs6565676	snp	G/T	0.49614	0.0437598	intron-variant	RNF213	GRCh38.p7	17:80326326	tttttagagcacttt[G/T]atgtgtacagaaaaa	57674
rs6565677	snp	C/T	0.427119	0.176434	intron-variant	RNF213	GRCh38.p7	17:80343642	CCAATTGTAAAACGG[C/T]GTATTTATGTGTCTA	57674
rs6565678	snp	A/G	0.442791	0.15916	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357847	AAAAATTAGCTGGGC[A/G]TGGTGGCACTGGGTG	57674
rs6565679	snp	C/T	0.211819	0.247067	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360717	GCTGAGCTCTGCTGC[C/T]AGATGCCAGAAGATT	57674
rs6565680	snp	A/G	0.485528	0.0838238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366804	tcaaacttggaacag[A/G]aaggaactctcctTG	57674
rs6565681	snp	A/G	0.321449	0.239573	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374694	ATGGACCACTGATGC[A/G]GCCCATCACGTGACA	57674
rs6565682	snp	A/G	0.251578	0.249995	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388469	TGGTGGGTTAATGAC[A/G]GAGAGGGGCGCTCTT	57674
rs6565683	snp	A/T	0.381503	0.21262	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388500	AGCCAAGGGATACAC[A/T]GGGCAGCGCGGCACT	57674
rs7206993	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287635	CCCCGACCCTGCCCA[C/T]CCCCCACTTTTGTTT	57674
rs7207660	snp	C/T	0.457154	0.139954	intron-variant	RNF213	GRCh38.p7	17:80341643	ctaggaaggctgact[C/T]gggaggatcgctcca	57674
rs7208006	snp	C/G/T	0.00127898	0.0252576	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361684	CTGGAGGCAGGGGAG[C/G/T]GCCATGACTTAGACG	57674
rs7208136	snp	C/T	0.427271	0.176281	intron-variant	RNF213	GRCh38.p7	17:80341931	cctgcctcagcctcc[C/T]gagtagctgggacta	57674
rs7209174	snp	A/T	0.452227	0.146984	intron-variant	RNF213	GRCh38.p7	17:80323949	cctgcaacattgctg[A/T]gctcatttggtagct	57674
rs7209233	snp	A/G	0.438526	0.164189	intron-variant	RNF213	GRCh38.p7	17:80335932	CAGTGAGCCGAGATC[A/G]TGTCACTTCACTCCA	57674
rs7209557	snp	C/T	0.441432	0.160792	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359636	TAAAGAAAGAAAGAG[C/T]GAGAGAAAGAAAGAA	57674
rs7209771	snp	C/G	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355442	GGGGTGGATGGGAAT[C/G]GGGGCTCACGGAGGA	57674
rs7211876	snp	C/T	0.32593	0.23819	intron-variant	RNF213	GRCh38.p7	17:80337560	GCTCCAACCGTGGCC[C/T]GTGTTCTCTCCTTTT	57674
rs7212829	snp	G/T	0.494568	0.0518327	intron-variant	RNF213	GRCh38.p7	17:80324800	TTGGTGTGTGTTTGT[G/T]TGTGTGTCTTCACAT	57674
rs7213539	snp	A/G	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80340841	acagagtctcactct[A/G]ttgcccagattggag	57674
rs7213699	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355408	GTGAATGGGAATGGG[A/G]GCTCACGGAGGAAGA	57674
rs7213818	snp	A/G	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355433	GGAAGAAGCGGGGTG[A/G]ATGGGAATCGGGGCT	57674
rs7214019	snp	A/G	0.485664	0.0834419	intron-variant	RNF213	GRCh38.p7	17:80261796	GGCCAAGGCGGGTGG[A/G]TCACCTGAGGTCGGG	57674
rs7214614	snp	A/G	0.43978	0.162738	intron-variant	RNF213	GRCh38.p7	17:80284995	TAGAGTAAGGCTGAT[A/G]TTACTCAAACCATGC	57674
rs7215078	snp	A/T	0.498009	0.0314867	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287290	TGCCTGAGCCTGAGA[A/T]TTCAAAACCAGCTTG	57674
rs7215243	snp	A/G	0.438666	0.164028	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288006	GCCGAGCCAGCCCCC[A/G]GGCACAGCCACCACG	57674
rs7216493	snp	A/G	0.445108	0.15631	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353558	TGAGGAGGCGATGGA[A/G]ACGGAGGCCAGCACA	57674
rs7217256	snp	A/G	0.49703	0.0384237	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355371	GTGAACGGGAATGGG[A/G]GCTTACAGGGGAAGA	57674
rs7217421	snp	A/G	0.476918	0.104919	intron-variant	RNF213	GRCh38.p7	17:80261661	AGCGGATTGAATGCA[A/G]CAGTGTTGGGTGCCT	57674
rs7219131	snp	C/T	0.489608	0.0713316	intron-variant	RNF213	GRCh38.p7	17:80278971	CATGCTGGCACAGCC[C/T]GGCACGGCCACCTCG	57674
rs7219660	snp	C/T	0.457388	0.139608	intron-variant	RNF213	GRCh38.p7	17:80279301	GGAGCCCAAGGGGGC[C/T]TAGAGGGCCAGGCCC	57674
rs7220243	snp	C/T	0.00203195	0.0318096	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288043	GAGGGTGACGGCCTC[C/T]CCGCGCCCACCGAGG	57674
rs7220465	snp	A/G	0.495708	0.0461266	intron-variant	RNF213	GRCh38.p7	17:80286212	TGTCGGACGCAGGCC[A/G]GTGTTGGACGCAGGC	57674
rs7221291	snp	C/T	0.485187	0.0847778	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370543	cagtagctggaggta[C/T]tgttttcttcaccgc	57674
rs7222014	snp	A/G	0.444267	0.157354	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319669	TTGCTCAGTAGGTGT[A/G]CGGGAAGAGACTCCA	57674
rs7222128	snp	C/T	0.42	0.183303	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355398	AAGAAGCGGGGTGAA[C/T]GGGAATGGGGGCTCA	57674
rs7223115	snp	C/T	0.444829	0.156658	intron-variant	RNF213	GRCh38.p7	17:80349957	CCCCAGCCGCAGCCG[C/T]GTGGCTTCTGCGTGG	57674
rs7223701	snp	G/T	0.212425	0.24716	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388851	CAGCAAATCAGCAAG[G/T]TTTCTTGTAGAGTAA	57674
rs7224239	snp	A/G	0.472522	0.113946	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381376	AACAGAAAAGCCAGC[A/G]GCCGTTCCGCTTGCT	57674
rs7224493	snp	C/G	0.458315	0.13822	intron-variant	RNF213	GRCh38.p7	17:80349020	GGAGGCCGCTGGAAC[C/G]GTACAAAGGAGAGGA	57674
rs7224585	snp	C/G	0.184838	0.241358	intron-variant	RNF213	GRCh38.p7	17:80335689	TGCTATTAACAGACA[C/G]TACAggctgggcgtg	57674
rs7225029	snp	A/G	0.180383	0.240111	intron-variant	RNF213	GRCh38.p7	17:80323979	tcaaattgtgtgtgc[A/G]tgtgtgtgtgtgtgt	57674
rs7501563	snp	A/G	0.495407	0.0477027	intron-variant	RNF213	GRCh38.p7	17:80326746	agctaacttcgtttt[A/G]ccactgaataatatt	57674
rs7501761	snp	A/T	0.499683	0.0125759	intron-variant	RNF213	GRCh38.p7	17:80316385	cagtttacaaaacag[A/T]tggcctgaacttttc	57674
rs7501767	snp	C/T	0.000477598	0.0154457	synonymous-codon	RNF213	GRCh38.p7	17:80291715	TCCTTACAAGTACGT[C/T]ATTTATAATGGGGAA	57674
rs7501942	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80292343	gaagtgttgggatta[C/T]aggtgtaagccacta	57674
rs7501987	snp	A/G	0.41141	0.19091	intron-variant	RNF213	GRCh38.p7	17:80317664	gcaggagcaagctcc[A/G]tgcaggccctgcagc	57674
rs7502336	snp	C/T	0.496968	0.0388195	intron-variant	RNF213	GRCh38.p7	17:80307970	ACTTGTAAATAGTCA[C/T]GATACTGCATATGCC	57674
rs7502410	snp	C/T	0.276534	0.248588	intron-variant	RNF213	GRCh38.p7	17:80316696	TGCCCAGGTATGTAG[C/T]GGCAAGGTGCCATGA	57674
rs7502437	snp	C/T	0.40263	0.198	intron-variant	RNF213	GRCh38.p7	17:80308348	ACACCGCCTTCCCAG[C/T]CCCCTCCATCAACTC	57674
rs7502832	snp	A/C	0.312837	0.241974	intron-variant	RNF213	GRCh38.p7	17:80302238	aacgactgtaattta[A/C]aatttattacgtttt	57674
rs7503136	snp	C/T	0.482905	0.0908579	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320426	ggtgcgatcctggct[C/T]accgcaaccgctgcc	57674
rs7503198	snp	A/G	0.0573587	0.15934	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365210	TCCAGAGCCCTCACC[A/G]CCAGGGGGTCTGGAA	57674
rs7503341	snp	A/G	0.499663	0.0129749	intron-variant	RNF213	GRCh38.p7	17:80316510	ATAAGTAAGTACAGC[A/G]TGTGTCCCAGGAGGA	57674
rs7503361	snp	A/G	0.0532157	0.154195	intron-variant	RNF213	GRCh38.p7	17:80302125	gtagttacgagaggc[A/G]aggaaggatggggag	57674
rs7503557	snp	C/T	0.202918	0.245527	intron-variant	RNF213	GRCh38.p7	17:80291868	CTCACCCCTCCGGAG[C/T]GCAGGTGCCAATCCC	57674
rs7503559	snp	A/C	0.217551	0.247885	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361014	GATCTTTCTGGCTTG[A/C]ATGCTCTGTGACCCC	57674
rs7503942	snp	C/T	0.499713	0.0119774	intron-variant	RNF213	GRCh38.p7	17:80300077	gtttttggtatatac[C/T]cagtaatgggattgc	57674
rs8066993	snp	C/T	0.398194	0.201342	intron-variant	RNF213	GRCh38.p7	17:80306230	TGCGTCTCTTTTCTC[C/T]GTCCCTATTTCTCTT	57674
rs8067125	snp	C/T	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80329875	ttgggtattaatagg[C/T]aggtctttcaactct	57674
rs8067292	snp	C/T	0.499117	0.0209873	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360040	CAAACCCTCTTCTTA[C/T]CATCCCTCACCTTAT	57674
rs8067570	snp	A/G	0.317692	0.240661	intron-variant	RNF213	GRCh38.p7	17:80300518	caaagttctaggatt[A/G]caggcatgagccacc	57674
rs8067782	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80300794	agacctcaagtgatc[C/T]gcccaccttggcctc	57674
rs8067940	snp	C/T	0.118235	0.212457	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360491	AGGGATATGGCGAAA[C/T]GGGGTGTGTTCTGGC	57674
rs8068939	snp	A/C	0.411578	0.190768	intron-variant	RNF213	GRCh38.p7	17:80301465	aagtgaacagaaaaa[A/C]tcagatctaaaaatg	57674
rs8069507	snp	C/T	0.490943	0.0666801	intron-variant	RNF213	GRCh38.p7	17:80280135	CCACTCCTGCAGCTC[C/T]TGGGAAATGCAGGCA	57674
rs8069705	snp	C/T	0.490119	0.0695896	intron-variant	RNF213	GRCh38.p7	17:80280268	GGATGGATTCATAGG[C/T]CATGCGAGGAGAAGA	57674
rs8070106	snp	A/G	0.482159	0.0927485	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370646	tttcaacgttttgtg[A/G]aaatgggaagcacac	57674
rs8070337	snp	A/G	0.0126979	0.078662	intron-variant	RNF213	GRCh38.p7	17:80282990	ggtgtgagccaccac[A/G]cctggccTGATTCAA	57674
rs8070547	snp	A/G	0.493925	0.054776	intron-variant	RNF213	GRCh38.p7	17:80275844	attttttgtattttt[A/G]gtagagacggggttt	57674
rs8070920	snp	A/G	0.494013	0.0543839	intron-variant	RNF213	GRCh38.p7	17:80300386	tctgctgggattggt[A/G]gtgtgcgccaccaca	57674
rs8071440	snp	C/T	0.299158	0.245119	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366319	tatgcagaggcactg[C/T]attgttttccacggg	57674
rs8071720	snp	C/G	0.219648	0.248151	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356162	ACCCACCACCACACC[C/G]AGCTACTTTTGGTAT	57674
rs8072622	snp	G/T	0.442249	0.159814	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359114	ATTCCCTGGTGGAGC[G/T]GCACAGCCCCCACCC	57674
rs8072756	snp	A/G	0.40386	0.197046	intron-variant	RNF213	GRCh38.p7	17:80279737	GCCTTCCAAAATGCT[A/G]GGATTACAGACGTGA	57674
rs8072774	snp	A/G	0.160918	0.233599	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389254	GAAGTGCTGTCTGTC[A/G]TAGAAGTCACTCTGG	57674
rs8072917	snp	C/T	0.499859	0.0083854	intron-variant	RNF213	GRCh38.p7	17:80335308	CTGTGGCTTAGATGT[C/T]GTTGGCAGAGGAGAG	57674
rs8073256	snp	A/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80280114	GGCTGGGGCTTGGCC[A/G]TGAGCCCACTCCTGC	57674
rs8074015	snp	A/G	0.458551	0.137864	missense	RNF213	GRCh38.p7	17:80332480	CCGTGGACCACCAGG[A/G]CCAAAGAGATTGGAT	57674
rs8074544	snp	A/G	0.465788	0.126237	intron-variant	RNF213	GRCh38.p7	17:80276256	caggcatgcaccacc[A/G]tgtctggctaatttt	57674
rs8075841	snp	A/G	0.17654	0.238964	intron-variant	RNF213	GRCh38.p7	17:80333492	tgaggtgaggagttc[A/G]agaccagcctgacca	57674
rs8076097	snp	A/G	0.162253	0.234095	intron-variant	RNF213	GRCh38.p7	17:80334838	tcactgtgttagcca[A/G]gatggtctcgatctc	57674
rs8076804	snp	A/G	0.317933	0.240593	intron-variant	RNF213	GRCh38.p7	17:80301682	agaaactctcataca[A/G]tgtaggaatgtaaat	57674
rs8077261	snp	A/G	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80286285	ATGGGTCGGAGGGTC[A/G]GGGGGTGGGGGCGCC	57674
rs8077408	snp	A/G	0.0256215	0.110247	intron-variant	RNF213	GRCh38.p7	17:80302030	tgaaataagccaggc[A/G]cagaaagagaaatac	57674
rs8077511	snp	A/C	0.030278	0.119257	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368456	ttttttttttgagac[A/C]gtgtttcactctgtt	57674
rs8077768	snp	C/T	0.489318	0.0722982	intron-variant	RNF213	GRCh38.p7	17:80282633	tggatctcctgacct[C/T]gtgatccacccgcct	57674
rs8078100	snp	G/T	0.033524	0.125053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360257	GGTGAATCACAAAGG[G/T]ATTGCCTGACAGTGA	57674
rs8078251	snp	A/G	0.495016	0.0496707	intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360406	GAGTGAGAGGCCCCG[A/G]CGGGACCAGAAACCT	57674
rs8078851	snp	C/T	0.497416	0.0358495	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352467	GAGAGTGGCGGGGGT[C/T]GGACTATCTTCAGAT	57674
rs8079586	snp	A/G	0.479421	0.0993283	intron-variant	RNF213	GRCh38.p7	17:80334985	ggagtgcagtggtgc[A/G]atctcggctcactgc	57674
rs8079692	snp	A/G	0.0126979	0.078662	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320446	caaccgctgcctccc[A/G]ggttcaagtgattct	57674
rs8079922	snp	A/G	0.247053	0.249983	intron-variant	RNF213	GRCh38.p7	17:80301545	caggcatatgaaaaa[A/G]tgatcagcatcatta	57674
rs8080730	snp	A/G	0.499732	0.0115784	intron-variant	RNF213	GRCh38.p7	17:80342809	CTCTGTCACCCTAAC[A/G]ATGACAACTGCACCC	57674
rs8081176	snp	C/T	0.495559	0.0469148	intron-variant	RNF213	GRCh38.p7	17:80310187	CCCGTCTCTGTGCAG[C/T]TTTCACCCACTTGAG	57674
rs8081340	snp	C/T	0.495708	0.0461266	intron-variant	RNF213	GRCh38.p7	17:80310307	gcccaggctggagtg[C/T]agtggcgccatctca	57674
rs8081918	snp	A/G	0.0437281	0.141251	intron-variant	RNF213	GRCh38.p7	17:80317085	TGTTCGCGGAGTCCC[A/G]CGCTCTCTGTATTGC	57674
rs8082521	snp	A/C	0.4629	0.131047	missense	RNF213	GRCh38.p7	17:80328357	TCACCCCAGGATGAA[A/C]AATGTGCTGTGGAGG	57674
rs9319624	snp	A/G	0.49681	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80293845	AAAAAAAAACATGTG[A/G]TAGGGGATTTGACCT	57674
rs9674807	snp	C/T	0.491629	0.0641526	intron-variant	RNF213	GRCh38.p7	17:80312377	CTGGTGGGTCCGGCA[C/T]GGAGGCGGGGGGAGA	57674
rs9674961	snp	A/G	0.476618	0.105566	missense	RNF213	GRCh38.p7	17:80345336	GTGTCGATGCCATCA[A/G]TCACTTGACTGGGAA	57674
rs9709240	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80338673	agataatttaaaaaa[A/T]ttaaaaCAGTCCAGG	57674
rs9889493	snp	C/T	0.222928	0.24853	intron-variant	RNF213	GRCh38.p7	17:80277368	ATTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA	57674
rs9889839	snp	A/G	0.483126	0.0902898	intron-variant	RNF213	GRCh38.p7	17:80296879	TAGAGACGGGGTTTC[A/G]CCATGTTGCCACGGT	57674
rs9890007	snp	A/C	0.488905	0.0736498	intron-variant	RNF213	GRCh38.p7	17:80277628	AAAAAGCCTAAATAT[A/C]CACATATCCACACAT	57674
rs9890495	snp	C/G	0.276617	0.248579	intron-variant	RNF213	GRCh38.p7	17:80294697	GGTCTTAGGTAGGCT[C/G]TTGTTCCTTCTGTCC	57674
rs9890733	snp	A/G	0.0356815	0.128715	intron-variant	RNF213	GRCh38.p7	17:80272982	CACTCGTGGACATTG[A/G]GAGGAAGAGGCTGGA	57674
rs9890817	snp	G/T	0.28052	0.24813	intron-variant	RNF213	GRCh38.p7	17:80318846	CCAAAGTGCTGGGAT[G/T]ACAGGCGTGAGCCAC	57674
rs9891036	snp	A/G	0.131381	0.220067	intron-variant	RNF213	GRCh38.p7	17:80267302	aaaaattagctaggc[A/G]tggtggcgtgtacct	57674
rs9891556	snp	C/T	0.0360663	0.129354	intron-variant	RNF213	GRCh38.p7	17:80272262	gcactccagcctggg[C/T]gacagagcaagactc	57674
rs9891691	snp	C/G	0.275464	0.2487	intron-variant	RNF213	GRCh38.p7	17:80295200	TACTGGTTGTAATCT[C/G]AGCCCCACCCCAGCA	57674
rs9891729	snp	C/T	0.0360663	0.129354	intron-variant	RNF213	GRCh38.p7	17:80265161	aagtgattcttctgc[C/T]tcagcctcccaagta	57674
rs9892846	snp	C/T	0.495963	0.0447464	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319841	GCTCCCTGCTGGCCA[C/T]GGCTGCCCTGCTCAC	57674
rs9892904	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80262139	CATTGAAGGTGTTTG[A/T]GGGAGGGAGTGTCCA	57674
rs9892914	snp	A/G	0.453331	0.145452	intron-variant	RNF213	GRCh38.p7	17:80342737	GTATATATATATTAT[A/G]TATATATTGTATGTA	57674
rs9893785	snp	C/T	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80290117	CCTGCTGGTGCCTCC[C/T]GCCACTGTCCCCAGC	57674
rs9895804	snp	C/G	0.22263	0.248497	intron-variant	RNF213	GRCh38.p7	17:80277733	CGCATTTTCCCAATC[C/G]CACAGGGAGCCTATT	57674
rs9895826	snp	A/T	0.216048	0.247684	intron-variant	RNF213	GRCh38.p7	17:80264500	TAAACACCAACCCTA[A/T]AACTAGCAGCCCCCA	57674
rs9896034	snp	A/G	0.290977	0.246619	intron-variant	RNF213	GRCh38.p7	17:80318825	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	57674
rs9896523	snp	C/G	0.487933	0.0767327	intron-variant	RNF213	GRCh38.p7	17:80278055	AGGGTGTCCTTTGTG[C/G]ATTCTTCCTCTGGAG	57674
rs9896984	snp	A/G	0.155656	0.231515	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351468	GGAAGAAAACGAGCC[A/G]CTAAGAGAAGATTTC	57674
rs9897381	snp	A/G	0.0203387	0.0987709	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374538	TCTCCGTGATGCTGT[A/G]GCCAAAGCTGTCCTC	57674
rs9897796	snp	C/G	0.241914	0.249869	intron-variant	RNF213	GRCh38.p7	17:80317083	GGTGTTCGCGGAGTC[C/G]CGCGCTCTCTGTATT	57674
rs9898470	snp	A/G	0.213333	0.247296	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377568	AAATTAGACTCAGAC[A/G]TTTTTCACTGACAAC	57674
rs9899091	snp	C/T	0.115438	0.210697	intron-variant	RNF213	GRCh38.p7	17:80325531	aaatggagaaggcaa[C/T]gcgacttacctaagg	57674
rs9899221	snp	C/T	0.15665	0.231917	intron-variant	RNF213	GRCh38.p7	17:80349700	TTTCTAGGATCTGTC[C/T]AAACCTGGCAGCAGA	57674
rs9901460	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80279720	ATGATCCACCCATCT[C/T]GGCCTTCCAAAATGC	57674
rs9901491	snp	A/G	0.22263	0.248497	intron-variant	RNF213	GRCh38.p7	17:80277719	TACAGGGGCTTTTGC[A/G]CATTTTCCCAATCCC	57674
rs9901492	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378938	cagcacttcaggagg[C/T]tgaggcaggtggatt	57674
rs9902013	snp	C/T	0.356597	0.226135	intron-variant	RNF213	GRCh38.p7	17:80272663	GAGTTTTGGTGGGGA[C/T]GGACAAAGTGCGTCC	57674
rs9902702	snp	A/G	0.484841	0.0857308	intron-variant	RNF213	GRCh38.p7	17:80272406	GGGCTTTTGTGCCAC[A/G]TGGCAGAGTAGGCCG	57674
rs9903254	snp	C/T	0.378765	0.214288	upstream-variant-2KB	RNF213	GRCh38.p7	17:80258851	ACTCCGGCCCAGCAC[C/T]ATTACGTGGGCAAGA	57674
rs9905368	snp	C/T	0.198014	0.244535	intron-variant	RNF213	GRCh38.p7	17:80279547	TCAGTTCACTGCAAC[C/T]TCCGCGTGCAGGGTT	57674
rs9905727	snp	A/G	0.317451	0.240729	intron-variant	RNF213	GRCh38.p7	17:80299014	ATCAAGAATACAGAA[A/G]CAACTTGTAACCTCA	57674
rs9907705	snp	G/T	0.184838	0.241358	intron-variant	RNF213	GRCh38.p7	17:80333310	cgtgatccacccacc[G/T]tggcctcccaaagtg	57674
rs9907978	snp	A/G	0.496105	0.0439572	intron-variant	RNF213	GRCh38.p7	17:80327580	TTGGCCATTGCGGGA[A/G]GTCATCTTCTTGGAC	57674
rs9908287	snp	C/G	0.489476	0.0717708	synonymous-codon	RNF213	GRCh38.p7	17:80332508	GATCAAGGACCGAGT[C/G]GAACAGATCAAGGAA	57674
rs9908583	snp	A/G	0.495855	0.045338	intron-variant	RNF213	GRCh38.p7	17:80327674	AGTGGAATGATTGGC[A/G]CATCTGGAGACACTG	57674
rs9909720	snp	C/T	0.267091	0.249415	intron-variant	RNF213	GRCh38.p7	17:80295312	GCGGTGCAGCCTGGG[C/T]GGGTTTCAGGCCGGC	57674
rs9911199	snp	A/G	0.0182019	0.0936463	intron-variant	RNF213	GRCh38.p7	17:80279553	cactgcaacctccgc[A/G]tgcagggttcaagcg	57674
rs9912419	snp	G/T	0.318896	0.240319	intron-variant	RNF213	GRCh38.p7	17:80298952	ctactgcactgtagc[G/T]tgggcgacagagcga	57674
rs9913317	snp	C/T	0.0101882	0.070642	missense	RNF213	GRCh38.p7	17:80273325	AGGAGGAAGGGGGCC[C/T]GTGCTTGTTCCCGGG	57674
rs9913473	snp	A/T	0.495252	0.0484902	intron-variant	RNF213	GRCh38.p7	17:80327021	TGCAAGATAATGAAG[A/T]TGTACAGAGTATAAA	57674
rs9913636	snp	C/G	0.492531	0.0606536	missense	RNF213	GRCh38.p7	17:80332302	CACATCCTTGAGCTT[C/G]AAGAGGTGTATGACT	57674
rs9913720	snp	C/T	0.495252	0.0484902	intron-variant	RNF213	GRCh38.p7	17:80327128	GGTATGTCTGCATCC[C/T]CTGGTGCAGTTTCTT	57674
rs9914404	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80267776	gttctccagatctgg[A/C]taaggttattgatgg	57674
rs9914778	snp	A/T	0.386313	0.209568	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366681	AATAAAAAAAAAAAA[A/T]TCTGTAAATGTCATC	57674
rs9914925	snp	A/G	0.0505692	0.150756	intron-variant	RNF213	GRCh38.p7	17:80261874	cacaaaaaattagcc[A/G]ggtgtggtggcgcat	57674
rs9915540	snp	A/G	0.494187	0.0535994	intron-variant	RNF213	GRCh38.p7	17:80293620	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	57674
rs9915562	snp	A/G	0.441705	0.160466	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358596	CAGAGCAACGTTGAC[A/G]TGGGTGCTTTCTGCA	57674
rs9916351	snp	C/T	0.487871	0.076925	intron-variant	RNF213	GRCh38.p7	17:80265733	ttagctgagttaaaa[C/T]gaaagctgagcttcc	57674
rs9944443	snp	A/T	0.485528	0.0838238	intron-variant	RNF213	GRCh38.p7	17:80350248	TTGGGGAATTTTCTT[A/T]TCCATTTTTTTAAGA	57674
rs9972886	snp	C/T	0.0322114	0.122752	intron-variant	RNF213	GRCh38.p7	17:80286532	GGGCCACACAGGGGC[C/T]GACCGTCAGCCGAGG	57674
rs10459966	snp	C/T	0.139225	0.224118	intron-variant	RNF213	GRCh38.p7	17:80293717	CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC	57674
rs10707823	in-del	-/A	0.489665	0.0711382	intron-variant	RNF213	GRCh38.p7	17:80324570	AGAAACTTTGAACCT[-/A]AAGGAAGAAAAATAT	57674
rs10782008	snp	A/G	0.488319	0.0755263	missense	RNF213	GRCh38.p7	17:80332071	AGATTAAATGACACC[A/G]TGACAGTGAGACTGT	57674
rs10871506	snp	A/G	0.492337	0.0614248	intron-variant	RNF213	GRCh38.p7	17:80282246	cagttgctacacggt[A/G]cggtgttgctctttg	57674
rs10871507	snp	G/T	0.492237	0.0618148	intron-variant	RNF213	GRCh38.p7	17:80282254	acacggtGCGGTGTT[G/T]CTCTTTGTGTTCTTT	57674
rs10871508	snp	C/T	0.492237	0.0618148	intron-variant	RNF213	GRCh38.p7	17:80282256	acggtgcggtgttgc[C/T]ctttgtgttctttgt	57674
rs11150853	snp	A/G	0.477441	0.103782	intron-variant	RNF213	GRCh38.p7	17:80268380	aaaaaaaaaaaaaaa[A/G]gcagtactgcatccc	57674
rs11150854	snp	A/G	0.427727	0.175821	intron-variant	RNF213	GRCh38.p7	17:80282699	CACTGCACCCGGCCT[A/G]TTATTACTATTTTTC	57674
rs11150855	snp	A/G	0.499879	0.0077866	intron-variant	RNF213	GRCh38.p7	17:80304407	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	57674
rs11150856	snp	C/T	0.158962	0.232835	intron-variant	RNF213	GRCh38.p7	17:80349082	ATTTGGCAGGGCCAA[C/T]ACCACCACCCAGTGG	57674
rs11306667	in-del	-/A	0	0	intron-variant	RNF213	GRCh38.p7	17:80295457	GTGGTGGGGCACGGA[-/A]TGGGGTCTGCTGCCC	57674
rs11340394	in-del	-/A	0.375	0.216506	intron-variant	RNF213	GRCh38.p7	17:80335977	AAAAAAAAAAAAAAA[-/A]CTACAAAAGATTAGG	57674
rs11383116	in-del	-/T	0.0711525	0.174681	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365937	GGAACGTGGGGAGGG[-/T]TTTTTTTTGGCGATA	57674
rs11389554	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368434	TGTAGACGCCAGTGT[-/T]TTTTTTTTTTTTTTT	57674
rs11424638	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369399	TGAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	57674
rs11431001	in-del	-/A	0	0	intron-variant	RNF213	GRCh38.p7	17:80325677	GCTGTCTGATTTCCC[-/A]CCCAGCCCCCCGCGC	57674
rs11455821	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80318579	ACTTTTTTTTTTTTT[-/T]GAGACGGGGTCTCGC	57674
rs11547133	snp	C/T	0.0588605	0.161139	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382118	ATTGATCCTTTGACA[C/T]GCACGCTCTGTGTGG	57674
rs11649963	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80318809	cgatctcctgacctc[A/G]tgatccacccgcctc	57674
rs11651635	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290483	tgcacgtgtgtgtgc[A/G]cacgtgtgtgtgtgc	57674
rs11651637	snp	A/G	0.348354	0.22984	intron-variant	RNF213	GRCh38.p7	17:80290499	CACGTGTGTGTGTGC[A/G]CGTGTGTGCATGCAC	57674
rs11651638	snp	A/G/T			intron-variant	RNF213	GRCh38.p7	17:80290501	cgtgtgtgtgtgcgc[A/G/T]tgtgtgCATGCACAT	57674
rs11653009	snp	C/G/T	9.05736e-05	0.00672894	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363828	CACTGCTTCATCTGG[C/G/T]GCGCGCTCACCAGGA	57674
rs11653704	snp	A/G	0.196771	0.244268	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384800	GGACGCGGCTGATGC[A/G]TCAGCTCCATAGAGG	57674
rs11654188	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341711	acactgcactccagc[C/T]taggcaacggggcaa	57674
rs11654408	snp	A/G	0.145642	0.227177	intron-variant	RNF213	GRCh38.p7	17:80350552	CCCAAGTGGGATTAG[A/G]GAAACTGAAGAGAGA	57674
rs11655038	snp	A/C	0.0715223	0.175059	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353429	CACTCGGAGGCTGAG[A/C]ACACAGACTCCCAGA	57674
rs11655596	snp	A/G	0.0737376	0.17729	intron-variant	RNF213	GRCh38.p7	17:80329630	gtctaggagtttgag[A/G]ccagcctgggcaaca	57674
rs11655696	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374207	GCGCCGCAAACGGAG[C/G]AAGCAAGCACCTCCC	57674
rs11655735	snp	C/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374280	TCTTCGTCTACTGAG[C/G]AGGAAGCTCCCTGCG	57674
rs11656211	snp	C/T	0.0755793	0.179102	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353945	CATTGAGACCCTCAT[C/T]GCATACGGGCGGTTT	57674
rs11657272	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80279628	tgccaccacgcccgg[C/G]tactttttttgtgta	57674
rs11658289	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80279993	CCAGCCCCTGCCCAT[C/G/T]GAGATGGTCATGTGT	57674
rs11658567	snp	A/G	0.496175	0.0435625	intron-variant	RNF213	GRCh38.p7	17:80261501	GCCCTGGGGGAGTCC[A/G]GGGCGGGAGGGGAAG	57674
rs11658902	snp	A/G	0.499879	0.0077866	intron-variant	RNF213	GRCh38.p7	17:80334336	GGCGCACTGTGTGGC[A/G]TTCCTAAACTCTTTG	57674
rs11867757	snp	A/G	0.426813	0.17674	intron-variant	RNF213	GRCh38.p7	17:80310442	atttttagtagagac[A/G]gggtttcaccatgtt	57674
rs11868105	snp	A/C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80312082	gcagtgagccaagat[A/C/T]gcgccactgtactcc	57674
rs11868385	snp	A/C/T	0.0123222	0.0776987	intron-variant	RNF213	GRCh38.p7	17:80292985	aaatttagtccctgt[A/C/T]actccaccttggaca	57674
rs11869363	snp	A/G	0.499598	0.0141716	intron-variant	RNF213	GRCh38.p7	17:80292960	GTTTTAGGCAGATAC[A/G]GAAGAATGTAAATTT	57674
rs11869583	snp	A/C	0.495407	0.0477027	intron-variant	RNF213	GRCh38.p7	17:80277074	acaaagcaaacaaac[A/C]aaaaaaaaaaCAaaa	57674
rs11869772	snp	A/C	0.47726	0.104176	intron-variant	RNF213	GRCh38.p7	17:80340725	TTCTGGGTTCAAGCA[A/C]TTATCCTGCCTCAGC	57674
rs11870829	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360280	GACAGTGAAAAGCAG[A/G]TGGGTGGCTAGAATT	57674
rs11871597	snp	C/T	0.093417	0.194889	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377947	CTCTGAGCAGGGCAA[C/T]GCCAATGGCGCTAAG	57674
rs12051723	snp	G/T	0.209997	0.246779	intron-variant	RNF213	GRCh38.p7	17:80350459	GTAGGAAGTCCTAGA[G/T]AATTTTTTCCTTGAA	57674
rs12051748	snp	C/T	0.422944	0.180528	intron-variant	RNF213	GRCh38.p7	17:80302352	tgtacacattataca[C/T]tgtatgcatatatat	57674
rs12051817	snp	A/G	0.471004	0.116864	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352143	CAGGTGTGAGCCACC[A/G]CACCCAGCCCAGTCA	57674
rs12051852	snp	C/T	0.4231	0.180378	intron-variant	RNF213	GRCh38.p7	17:80302320	tgtttgagatagata[C/T]gctaattaccctgat	57674
rs12051855	snp	C/T	0.439918	0.162576	intron-variant	RNF213	GRCh38.p7	17:80302637	CAGGCAGGAGGATTG[C/T]TTGAGGCCAGGAGTT	57674
rs12150356	snp	C/G	0.478104	0.102316	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365174	TGCCTCACCCGCACC[C/G]GTGACCTTCACGTGA	57674
rs12150357	snp	C/T	0.491263	0.0655142	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365209	ATCCAGAGCCCTCAC[C/T]GCCAGGGGGTCTGGA	57674
rs12449863	snp	C/T	0.390838	0.206555	intron-variant	RNF213	GRCh38.p7	17:80269412	gtcCTATCATCTATC[C/T]Atccatccatccatt	57674
rs12450169	snp	C/T	0.334871	0.235153	intron-variant	RNF213	GRCh38.p7	17:80292198	CAAGCAGTTCTCCTG[C/T]CTCAGCCTCCCGAGT	57674
rs12450267	snp	C/T	0	0	synonymous-codon	RNF213	GRCh38.p7	17:80340211	CAGCCAGCACAAGGT[C/T]TTCGTCACCCCCCAG	57674
rs12451223	snp	A/G	0.466927	0.124269	intron-variant	RNF213	GRCh38.p7	17:80305534	acagggctaccccat[A/G]ggagcatgcccagaa	57674
rs12451808	snp	A/G	0.494774	0.0508504	intron-variant	RNF213	GRCh38.p7	17:80303514	TCTTGCCTTTAGAAG[A/G]CGTAAAAGCCTTTGG	57674
rs12452908	snp	C/G	0.128632	0.218563	intron-variant	RNF213	GRCh38.p7	17:80279341	GGGGCCCGACCCAGC[C/G]TCTGCCTGAACACAA	57674
rs12453330	snp	C/G	0.336017	0.234736	intron-variant	RNF213	GRCh38.p7	17:80292238	TACAGGAGCCTGTCA[C/G]CACCCCCAGCTAACT	57674
rs12453681	snp	C/T	0.490508	0.0682328	intron-variant	RNF213	GRCh38.p7	17:80307775	GGCTGGTCTTGAACT[C/T]CTGACCTCAGGTGAT	57674
rs12600732	snp	A/T	0.0115144	0.0749975	intron-variant	RNF213	GRCh38.p7	17:80279452	CTGACTTTTTCTCTT[A/T]ttcttttctttcttt	57674
rs12600923	snp	C/T	0.499997	0.00119808	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355435	AAGAAGCGGGGTGGA[C/T]GGGAATCGGGGCTCA	57674
rs12601017	snp	A/G	0.190519	0.242821	intron-variant	RNF213	GRCh38.p7	17:80283113	AAAATTATAAATACC[A/G]CTATGGTTATGTAGT	57674
rs12601730	snp	A/C	0.190205	0.242744	intron-variant	RNF213	GRCh38.p7	17:80281798	gatgcccagtcccag[A/C]tatgaaacggcgtgg	57674
rs12601988	snp	A/G	0.444444	0.157135	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355653	GGAAGAAGCGGGGTG[A/G]ACGGGAATGGGGGCT	57674
rs12602569	snp	C/T	0.190205	0.242744	intron-variant	RNF213	GRCh38.p7	17:80283546	TGCCTCCAGCCTCCC[C/T]GGGCTCTGCCCAACC	57674
rs12603539	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355655	AAGAAGCGGGGTGGA[C/T]GGGAATGGGGGCTTA	57674
rs12603543	snp	A/G	0.198944	0.244731	intron-variant	RNF213	GRCh38.p7	17:80270110	TGCGTGAATGTGTGC[A/G]CACACACACACACGT	57674
rs12603583	snp	C/G	0.18325	0.240924	intron-variant	RNF213	GRCh38.p7	17:80270438	CTCTTCAAATCCCCT[C/G]CACAAAGCTTCTCTG	57674
rs12603603	snp	C/T	0.482309	0.0923707	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383259	CCAAGTGCTCTTCCC[C/T]CCTACAGCTGGTCAT	57674
rs12603671	snp	A/G	0.0865458	0.189163	intron-variant	RNF213	GRCh38.p7	17:80317901	catccaagaagaatg[A/G]ggtcacccggacact	57674
rs12603932	snp	A/C	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355692	GAAGAAGCGGGGTGA[A/C]CGGGAATGGGGGCTT	57674
rs12604017	snp	A/G	0.00966161	0.0688292	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394635	ATTCATTCTAAATGA[A/G]TTAACGACTTAACTT	57674
rs12936624	snp	C/G	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396745	CCCCACCCCCCCCCC[C/G]CAACCAGAGCAACTT	57674
rs12937063	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80310151	TGTCTGTGTGGTGCA[A/G]AGATCGGCAATTCCT	57674
rs12937242	snp	A/G	0.267636	0.249377	intron-variant	RNF213	GRCh38.p7	17:80294495	TCCACTCATTACTGT[A/G]GGACGTCTAGGATGT	57674
rs12938065	snp	G/T	0.193653	0.243567	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398325	atgttttgtcttgaa[G/T]aagcatgggtcaagc	57674
rs12939230	snp	A/G	0.206642	0.246211	intron-variant	RNF213	GRCh38.p7	17:80289188	TGAGGCTGGAGAGAG[A/G]CGCCTCTGGAGGCTG	57674
rs12942629	snp	C/T	0.338523	0.233803	intron-variant	RNF213	GRCh38.p7	17:80290482	GTGCACGTGTGTGTG[C/T]GCACGTGTGTGTGTG	57674
rs12943001	snp	C/T	0.398894	0.200825	intron-variant	RNF213	GRCh38.p7	17:80264846	TGGCTCCCTCTCCTG[C/T]CCCCAGAGCCCACCA	57674
rs12943016	snp	G/T	0.498182	0.0300969	intron-variant	RNF213	GRCh38.p7	17:80285687	TGCTTTTTTTTTTTT[G/T]TGAGATGGAGTCTTG	57674
rs12943133	snp	A/G	0.0368353	0.130617	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396620	CCATGATTAGCATTT[A/G]TATTGCATTCTGCAT	57674
rs12944088	snp	A/G	0.0295034	0.117819	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383678	TTTTCTCCATCCAGC[A/G]TCTAGATAAAACCCT	57674
rs12944385	snp	A/G	0.0148782	0.0849572	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383800	CCCCACCTGCCCCGG[A/G]AAAGTGTGGTCCATT	57674
rs12944949	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80269628	atctgtctatccatt[A/C]atctagcttatctat	57674
rs12945030	snp	A/G	0.0298908	0.118541	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374197	GTGGTGCGGTGCGCC[A/G]CAAACGGAGGAAGCA	57674
rs12945169	snp	A/G	0.162909	0.23434	intron-variant	RNF213	GRCh38.p7	17:80309284	GGGATGAGATGGAGC[A/G]GTGGTTTCAGCAGTG	57674
rs12946672	snp	C/T	0.0310518	0.120672	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367684	TGGTGCTCCCTCTGT[C/T]GCCCGGCCTGGCCGC	57674
rs12947095	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80310076	ATCAGTTTTACCTGT[C/T]TTCCAGCTTTGACCT	57674
rs12947158	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310139	GTCTCTGAGCTCTGT[C/T]TGTGTGGTGCAGAGA	57674
rs12947173	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80310156	GTGTGGTGCAGAGAT[C/G]GGCAATTCCTTCTTT	57674
rs12947285	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80340862	cagattggagtacag[G/T]ggcgtgatctcggct	57674
rs12947574	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80273968	CTCGTGTGTCTCCCA[A/G]AAGCTGTGGCTGGGG	57674
rs12947578	snp	C/T	0.449218	0.151037	intron-variant	RNF213	GRCh38.p7	17:80272935	GAGGTGCCCGAGGTG[C/T]GCTGACATCCTAGTA	57674
rs12947691	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80275439	taaacccgcccaaag[A/G]cagaggaaaagctaa	57674
rs12948960	snp	A/G	0.00477324	0.0486193	intron-variant	RNF213	GRCh38.p7	17:80268633	tccatccatccatcc[A/G]tccgtttatctgtct	57674
rs12949523	snp	C/T	0.490453	0.0684267	intron-variant	RNF213	GRCh38.p7	17:80269456	tatccatccatctat[C/T]catccatccattcat	57674
rs12949806	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269541	tttctattcatccat[C/T]catctatccatctat	57674
rs12950091	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80269627	catctgtctatccat[C/T]catctagcttatcta	57674
rs12950275	snp	C/T	0.392325	0.205532	intron-variant	RNF213	GRCh38.p7	17:80297914	ATGATCGCACCACCG[C/T]GCTGCCTTGATGACA	57674
rs12950573	snp	A/G	0.499354	0.0179596	intron-variant	RNF213	GRCh38.p7	17:80313475	GAGGTGATGGTGGTG[A/G]AGGTGATGGTGATGG	57674
rs12952231	snp	A/T	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287207	ctacagaGCATTTTT[A/T]AAAACCagctgggaa	57674
rs12952240	snp	C/T	0.199254	0.244796	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366604	ACAAAGTTATTAGGa[C/T]attaaaaatacacac	57674
rs13341393	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80338959	tctcaaaaaaaaatt[A/T]aaaaaaaaaaaaaaT	57674
rs13342364	snp	C/T	0.162253	0.234095	intron-variant	RNF213	GRCh38.p7	17:80337021	CTCCGGACGGCTGCT[C/T]TGCATGTGGGTGGAG	57674
rs17853713	snp	A/G	0.295195	0.245881	synonymous-codon	RNF213	GRCh38.p7	17:80289715	AGAAAAAGTCGGTAA[A/G]AATGAACAAGGGGAG	57674
rs17853714	snp	A/G	0.339962	0.233253	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287931	TTTGCTTTCAAACCC[A/G]TGGCCTCAGGACACA	57674
rs17853989	snp	C/T	0.294822	0.245949	missense	RNF213	GRCh38.p7	17:80289687	AGACCAAGGACGAGA[C/T]GGCTGCTGCTGAAGA	57674
rs17857134	snp	G/T			missense	RNF213	GRCh38.p7	17:80289832	TGTCCAGGAAGTGAA[G/T]GCAAGGTAGGGATGC	57674
rs17857135	snp	C/T	0.267755	0.249369	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288362	GGGCCTCAGCCTCTA[C/T]GGTGAGTCATCCGGG	57674
rs28366412	snp	A/G	0.0410537	0.137264	intron-variant	RNF213	GRCh38.p7	17:80302321	GTTTGAGATAGATAT[A/G]CTAATTACCCTGATT	57674
rs28367176	snp	A/G	0.357024	0.225933	intron-variant	RNF213	GRCh38.p7	17:80274550	CTCCATGGTTGGGCT[A/G]TGGTGGGAAGTGATG	57674
rs28371996	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281245	CACTCACACACACCT[C/T]AACACACATACCCCA	57674
rs28377805	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80274627	GGGGTGAGTGGGGTG[A/T]CTGTGGGGGGTGTGG	57674
rs28391226	snp	A/G	0.138886	0.22395	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396710	GCTGGAAAAACAAGC[A/G]CCAGGAAAGTGCATT	57674
rs28408154	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80274803	GATGAGTGGGGTGAG[G/T]GGGGGGTGAGGGGGG	57674
rs28411079	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80274628	GGGTGAGTGGGGTGT[C/G]TGTGGGGGGTGTGGG	57674
rs28437128	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80335648	GGGACATTGAAATTG[C/T]TCAGGAACGGCAAGA	57674
rs28453804	snp	A/G	0.117188	0.211804	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392936	TCTGCTGATGACAAC[A/G]GGAAAAAGTAACATG	57674
rs28494520	snp	C/T	0.322245	0.239334	intron-variant	RNF213	GRCh38.p7	17:80311571	GCACCTGCATCCTGG[C/T]CCCTCTTACATGCTT	57674
rs28522812	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274656	GGGGTGAGTGTGTGG[A/G]GTGAGTGGGGTGAGT	57674
rs28528832	snp	C/T	0.174288	0.23826	intron-variant	RNF213	GRCh38.p7	17:80311517	TGTGCTCTAGTCACT[C/T]CTGTGCCCAGCCCCC	57674
rs28571613	snp	C/G	0.20111	0.245173	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387514	CATTAGCTGTGCCTT[C/G]TGTGTGTCCTCACCT	57674
rs28580003	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80274653	TGTGGGGTGAGTGTG[G/T]GGGGTGAGTGGGGTG	57674
rs28670041	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80276284	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCTCC	57674
rs28678370	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80309759	TTTTTTTTTGTTTTT[G/T]GTTTTTTGTTTTTTA	57674
rs28767029	snp	A/G	0.34659	0.230587	intron-variant	RNF213	GRCh38.p7	17:80268637	TCCATCCATCCATCC[A/G]TTTATCTGTCTATCT	57674
rs28771970	snp	A/G/T	0.0682835	0.172094	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320047	GTTCGTATGCCATAC[A/G/T]GTACATCTGTCAAAA	57674
rs33976036	in-del	-/TA	0.382279	0.212137	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390720	CATATATTCTAATTT[-/TA]TAACAAGTAGACTAT	57674
rs34002630	snp	A/G	0.482979	0.0906686	intron-variant	RNF213	GRCh38.p7	17:80338629	TCTCAAAAAGTATAA[A/G]GTTTTTTTTTTTCCC	57674
rs34016996	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80264840	TCCTCTTGGCTCCCT[C/T]TCCTGCCCCCAGAGC	57674
rs34023913	snp	C/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357732	ATCCCAATACTTTGG[C/G]AGGCCAAGGCGGGAG	57674
rs34053469	in-del	-/CC/CT/CTCT	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80342555	TCTCTCTCTCTCTCT[-/CC/CT/CTCT]ATTTTTATATATATA	57674
rs34071383	in-del	-/C			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259378	AGGCTGAGGCATGAG[-/C]AATCACTTGAACTGG	57674
rs34071991	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80311959	GGTGAAACCCTGTCT[-/G]CTACTAAAAAATACA	57674
rs34095585	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382317	GTTATCTGTGAGTGG[C/T]GGAATTAAGAGTGAT	57674
rs34105320	in-del	-/GTTT	0.490836	0.0670685	intron-variant	RNF213	GRCh38.p7	17:80307543	AATTTTTGTGTGTTG[-/GTTT]GTTTGTTTGTTTGTT	57674
rs34155220	snp	C/T	0.349452	0.229367	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287177	CCAGCCTGAGCAACA[C/T]GGGAGACTCTGCCTC	57674
rs34163146	snp	C/G	0.033499	0.125771	intron-variant	RNF213	GRCh38.p7	17:80284756	TTCCCGTTACTCCCT[C/G]GTGCCACACAGTGGC	57674
rs34198427	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80283110	CGTAAAATTATAAAT[-/A]CCGCTATGGTTATGT	57674
rs34200106	in-del	-/T	0.47666	0.105476	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287179	GCCTGAGCAACATGG[-/T]GAGACTCTGCCTCTA	57674
rs34235051	in-del	-/T	0.493969	0.05458	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371010	ATTAATGAATATGGA[-/T]TTTTTTTTTTAAAAC	57674
rs34269699	snp	A/G	0.0770498	0.180522	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353909	TTGTCCGTGAGGACC[A/G]CCGCCCTGTGCTGTT	57674
rs34308274	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80350157	TTGGGTTTCCTCCCC[-/C]TGGACTATCTGTTCT	57674
rs34364611	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380298	CACATTCTGACTGTT[-/C]CCCTGCAGTCACAGC	57674
rs34371330	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80268471	CCCATTCACCTCCCC[-/C]TATTTGGCCTTTGTG	57674
rs34371653	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80329410	TGTGGCTATGTATGG[-/G]AGAAGTCCGATGCAG	57674
rs34397069	snp	C/T	0.337614	0.234145	intron-variant	RNF213	GRCh38.p7	17:80290382	GTGTGAGTGCGTGCA[C/T]GTGTGTGCGTGTACG	57674
rs34399489	snp	C/T	0.0290754	0.117014	synonymous-codon	RNF213	GRCh38.p7	17:80339762	CCCGACTGCCTCGAC[C/T]TAGAGACCCTTGGCC	57674
rs34401044	in-del	-/A	0.39527	0.203462	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395240	TGGCCTAGCAGAGGC[-/A]AAAAAAAAAAAAATG	57674
rs34576305	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80285041	AGCCAAGGGACCATT[-/C]CCCCAGGATGGGCCA	57674
rs34609464	snp	A/G	0.177503	0.239258	intron-variant	RNF213	GRCh38.p7	17:80292165	TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCCAGG	57674
rs34658156	in-del	-/C			frameshift-variant	RNF213	GRCh38.p7	17:80343946	TGGCTTCGGAACCCC[-/C]TGCCATTTGTATATC	57674
rs34659718	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80277596	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	57674
rs34714843	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371156	TATTTAAAGTATGGG[C/T]AGACCTTTTTGATTT	57674
rs34733680	in-del	-/AT/GT	0	0	intron-variant	RNF213	GRCh38.p7	17:80290414	TGCTTGTGTGTGTGC[-/AT/GT]GTGTGTGCGAGTGTG	57674
rs34755299	in-del	-/G			frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383797	TGCCCCACCTGCCCC[-/G]GGAAAAGTGTGGTCC	57674
rs34758627	snp	A/C	0.0693013	0.172766	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387820	TGACCTCATGCACTG[A/C]AGCCACACAGCAGGC	57674
rs34801706	snp	C/G	0.207864	0.246424	intron-variant	RNF213	GRCh38.p7	17:80290057	GGTCCTGGAGCCAGC[C/G]TGGGCCTTTGGGAAC	57674
rs34814288	in-del	-/CT			intron-variant	RNF213	GRCh38.p7	17:80342546	ATTTTTCTCTCTCTC[-/CT]TCTCTCTCTATTTTT	57674
rs34863514	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80284194	AAACCCCATCTGTAC[-/A]AAAATACAAAAAAAA	57674
rs34876847	in-del	-/T	0.387832	0.208572	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392606	CTCAGGATTTCTGGG[-/T]TTTTTTTTTTTCTCG	57674
rs34888554	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80286591	GTGGCGCTTCCTCAT[-/C]CCCCTTGTTACCAGT	57674
rs34907722	snp	G/T	0.384017	0.211044	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365818	GGAGATGCACAGGGC[G/T]TTCAGCCAGGTCCAG	57674
rs34937722	in-del	-/A/AA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369398	GTGAAACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA	57674
rs34984379	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80344531	AAAGATATGCTGTGG[-/G]AAAAAAAGACTATAC	57674
rs35029063	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80264089	AGGGCCAGGGCAGGG[-/T]AGAGGACAAAACAAG	57674
rs35037970	in-del	-/T	0.455858	0.141853	intron-variant	RNF213	GRCh38.p7	17:80305617	TCCTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC	57674
rs35057778	snp	C/G	0.342806	0.232136	intron-variant	RNF213	GRCh38.p7	17:80290432	GTGTGCGAGTGTGCG[C/G]GTGTGTGCATGTGTG	57674
rs35103191	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80262063	GTCTGTGGTTCCCCA[G/T]TGTAGCATTGGAGAA	57674
rs35123146	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80295366	CTGAGCCCTGATGAG[-/C]CTCAGGGGCCCTGCC	57674
rs35126635	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359416	GTAGTCCCAGCTACT[C/T]TAGAAGCTGAGGCGG	57674
rs35168579	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80264866	AGAGCCCACCACCTT[C/T]TGGCCCTTCCTGGAT	57674
rs35187522	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372315	TAGATAATTTTTTTT[-/T]CCTCATAGGTTCACT	57674
rs35192548	snp	C/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259339	CAGGCTTGGTGGCGG[C/G]CGCTTGTAATCCCAG	57674
rs35199608	in-del	-/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353081	CACGAGGCGGAGCCC[-/C]TGGGGGAGCAGGTGG	57674
rs35215667	snp	C/T	0.0256215	0.110247	intron-variant	RNF213	GRCh38.p7	17:80327046	TATAAAGTTATCACA[C/T]GGCTGTTTCTCTTTT	57674
rs35224052	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80263476	TTGAGAGCCAAGGGG[-/G]CAGCACAGAGCGGGG	57674
rs35242451	in-del	-/A	0.440471	0.161928	intron-variant	RNF213	GRCh38.p7	17:80338649	TTTTTTTTCCCAATT[-/A]AAAAAAAAAGATAAT	57674
rs35282118	in-del	-/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353120	AGATGGCAGGTGTGG[-/G]AGCGTGGCGTGCACA	57674
rs35294609	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80309519	TCTTTTTTCTTGATT[-/A]CTGTTGTTTGCAGAG	57674
rs35332090	snp	C/G	0.19401	0.24365	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363258	ACCATCTACCCTCAG[C/G]TTCTCCACAGCCTGA	57674
rs35344484	in-del	-/T/TT	0.282105	0.24793	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356923	GGGTTTTTTTTTTTT[-/T/TT]CGAGACAGAGTCTCA	57674
rs35429770	snp	C/G/T	0.00119752	0.0244452	intron-variant	RNF213	GRCh38.p7	17:80316769	CATTTGTGCAGAGTC[C/G/T]GAAGAGGGAGCACAG	57674
rs35493894	in-del	-/A			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286948	TGGCTGTGCCTGCTG[-/A]AGGGTGCGGTGGGAG	57674
rs35509053	in-del	-/CT	0.0372196	0.131242	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356346	TCCCCGGGACCAGCC[-/CT]GAGTCACTGAACCTC	57674
rs35516644	in-del	-/AT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390721	ATATATTCTAATTTT[-/AT]AACAAGTAGACTATG	57674
rs35557889	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80310648	CCTCCGCCTCCTGGG[-/G]TTCAAGTGATTCTCC	57674
rs35569924	in-del	-/A/AA	0.430285	0.173197	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382188	TGTTAAAAAAAAAAA[-/A/AA]GCTATAAAATATTGT	57674
rs35573434	snp	A/G	0.34303	0.232046	intron-variant	RNF213	GRCh38.p7	17:80291092	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	57674
rs35601285	in-del	-/C			frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368133	CTCCAGCTGTTTCCC[-/C]AAGCGCACAGGTACA	57674
rs35620096	in-del	-/AG	0.0876345	0.190099	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397380	AATTTCTGCCTCCAA[-/AG]AGAGAAGTAAAAACT	57674
rs35692831	snp	C/T	0.446118	0.155041	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259483	AAAACAAACAAACAA[C/T]AAATAAAGTGCCACC	57674
rs35702111	snp	A/G	0.031825	0.122064	intron-variant	RNF213	GRCh38.p7	17:80264902	AGGTGTGCTTCCACC[A/G]CAGGGCCTTTGCACC	57674
rs35707647	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80277812	GACGCCGCATTCTAA[-/C]CCATGGTGAGGAGGG	57674
rs35727324	in-del	-/C			frameshift-variant	RNF213	GRCh38.p7	17:80339579	AAAGCAACTGCACCC[-/C]TGAGGGATGTCTTAA	57674
rs35732656	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386514	ACAAGCAAGCTTCAG[-/C]CCCTTCCCTAACAGA	57674
rs35752463	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80267946	GCCTCAGCCTCCCAA[-/A]GTAGCTGGGATTACA	57674
rs35786093	snp	A/G	0.496483	0.0417852	intron-variant	RNF213	GRCh38.p7	17:80292614	CTCTGCCCATCTGTC[A/G]ATAGACGCGGGCGCT	57674
rs35800595	snp	C/T	0.0232847	0.105357	intron-variant	RNF213	GRCh38.p7	17:80332725	CTTTGAAAAGGGGGG[C/T]GGATGACTTAGAGCT	57674
rs35802586	in-del	-/A			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371125	GAAATCATGTGGGTC[-/A]AAAAAGAAAAAAATC	57674
rs35864932	snp	C/T	0.499295	0.0187567	intron-variant	RNF213	GRCh38.p7	17:80308082	ATTTGCTCCTGCAAA[C/T]TTGTGACCTCTGATA	57674
rs35883361	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80327151	GTTTCTTCTGTTGTA[-/A]GGTATTCCTAGGGCA	57674
rs35912728	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80331406	TTTTTTTTTTTTTTT[-/T]GATATGGAGTCTCAC	57674
rs35943283	in-del	-/TTCT	0.392696	0.205275	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365436	AGGTGCCCACGCTCC[-/TTCT]GTCTTGTCCCTTCAT	57674
rs35968416	snp	C/T	0.293551	0.246177	intron-variant	RNF213	GRCh38.p7	17:80326413	ACCCTGTTAGTAACA[C/T]GCAGCATTAGTGTGG	57674
rs35985211	in-del	-/GTG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359502	ACTCTAGCCTGGGTG[-/GTG]ACAGAGTGAGACTCT	57674
rs35993981	snp	A/T	0.480144	0.097642	intron-variant	RNF213	GRCh38.p7	17:80349645	TGGGTTTGGATTCTG[A/T]GCCGTTGTGTGGCAA	57674
rs36046948	snp	A/G	0.0341076	0.126057	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389911	ACAGCTGCTGCGGCT[A/G]CACAAAGTAAGTCTG	57674
rs36054053	snp	A/G	0.0298908	0.118541	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373726	GCCAGGCTGGGCACA[A/G]TGGCTCTCACCTGTA	57674
rs36099311	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389758	GAGAGCACTCAGGCT[-/C]CCCTGGTGCACGACA	57674
rs36101625	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80285400	GCAGCTGGCCGGGCA[-/G]GGGACGGCGTCATCG	57674
rs36103733	snp	C/T	0.202035	0.245356	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364093	AAAGGACACCCCGGG[C/T]GGGCAGGTGCACAGA	57674
rs55635150	snp	G/T	0.375	0.216506	intron-variant	RNF213	GRCh38.p7	17:80315899	TGGTGGTGGTGAAGG[G/T]GATGGTGGTGATGGA	57674
rs55692616	snp	A/C	0.453453	0.145282	intron-variant	RNF213	GRCh38.p7	17:80349136	GGGGCGACCCCCTGG[A/C]TTCCTCCTTAGATGA	57674
rs55727101	snp	C/G	0.487746	0.0773096	intron-variant	RNF213	GRCh38.p7	17:80315847	GTGATGGTGGTGGTG[C/G]TGGTGGTGGAGGTGA	57674
rs55731085	snp	A/G	0.163236	0.234461	intron-variant	RNF213	GRCh38.p7	17:80334446	CATAGAGTTCACACC[A/G]GTACAGTATTTCCCA	57674
rs55742494	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387971	TTTTTTTTTTTTTTT[C/T]TTTTTTGAGACGGAG	57674
rs55767628	snp	C/G	0.255224	0.249945	intron-variant	RNF213	GRCh38.p7	17:80319077	AGAAGCTTAAAATTG[C/G]GGGAAACAGTAAAAC	57674
rs55779209	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80307876	TTTTTTTTTTTTTTT[-/TT]AAAGGGAAATAATAG	57674
rs55814957	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80265061	TTTTTTTTTTTTTTT[-/TT]AGAGGGAGTTTTTTT	57674
rs55820068	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315815	TGGAGGTGGTGGTGG[A/T]GGTGGTGGTGGTGAT	57674
rs55874836	snp	A/G	0.0410537	0.137264	intron-variant	RNF213	GRCh38.p7	17:80301551	TATGAAAAAATGATC[A/G]GCATCATTAATTAGG	57674
rs55909171	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80322162	CCCCCCACCCCCCCT[C/T]TTTTTTTTTTTTTTT	57674
rs55971860	snp	A/G	0.34437	0.231505	intron-variant	RNF213	GRCh38.p7	17:80293430	AATAGGCATTAGTCC[A/G]GTAATTCCATATATA	57674
rs55996424	snp	A/T	0.36199	0.223514	intron-variant, missense	RNF213	GRCh38.p7	17:80319389	AGCTAAGGGCTATGA[A/T]GCACCCGCTGGGTCT	57674
rs56010739	snp	A/G	0.198014	0.244535	intron-variant	RNF213	GRCh38.p7	17:80349101	ACCACCCAGTGGGGG[A/G]ATGGGGGGTGGAGGG	57674
rs56056781	snp	A/G	0.41833	0.184838	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355580	GAAGAAGCGGGGTGA[A/G]TGGGAATGGGGGCTT	57674
rs56075150	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80277434	GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAG	57674
rs56102463	snp	C/G	0.21695	0.247806	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359908	GTCATAACAGAAACC[C/G]TGTACTGTGAAACAG	57674
rs56127781	snp	C/T	0.480144	0.097642	intron-variant	RNF213	GRCh38.p7	17:80349511	CCAAGCAGGCAGAGA[C/T]ACGGGCCTCTGGGGA	57674
rs56151266	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315820	GTGGTGGTGGTGGTG[A/G]TGGTGGTGATGGTGA	57674
rs56218925	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315751	ATGGTGGTGGTGGTG[A/G]AGGTGACAGTGGTGA	57674
rs56273945	snp	C/T	0.124144	0.21601	intron-variant	RNF213	GRCh38.p7	17:80308638	TCCACACGGGCTGCA[C/T]GCTCTTCTACTATTT	57674
rs56302457	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80340968	CACCAGTACACCCAG[A/C]TAATTTTTTTATTTT	57674
rs56376128	in-del	-/TG/TTGTAT/TTGTTG/TTGTTT/TTGTTTG			intron-variant	RNF213	GRCh38.p7	17:80265043	CTTCCATGTTTGTTT[lengthTooLong]GTTTTTTTTTTTTTT	57674
rs56700002	in-del	-/AA			intron-variant	RNF213	GRCh38.p7	17:80277616	AAAAAAAAAAAAAAA[-/AA]GCCTAAATATCCACA	57674
rs56790594	snp	A/G	0.0279526	0.114869	intron-variant	RNF213	GRCh38.p7	17:80291059	TCAGGTGATCCGCCC[A/G]CCTAGGCCTCCCAAA	57674
rs56831181	in-del	-/TAAA			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396269	CTGTCTCAAAAAAAA[-/TAAA]ATAAAATAAGGACCT	57674
rs56957242	in-del	-/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80273636	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC	57674
rs56976962	in-del	-/GTT			intron-variant	RNF213	GRCh38.p7	17:80265047	CATGTTTGTTTGTTT[-/GTT]TTTTTTTTTTTTTTA	57674
rs57148060	snp	C/T	0.18325	0.240924	intron-variant	RNF213	GRCh38.p7	17:80269753	ATCCATCCCATCTTA[C/T]CTATCCATCCGTCCA	57674
rs57271953	in-del	-/T	0.376195	0.215812	intron-variant	RNF213	GRCh38.p7	17:80291263	TTTTTTTTTTTTTTT[-/T]AGAGAGGGGATCTTG	57674
rs57282254	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313710	AAGGGGATGGTGGTG[A/G]TGGAGGTGGTGGTGG	57674
rs57381377	in-del	-/T	0.492582	0.0604491	intron-variant	RNF213	GRCh38.p7	17:80334617	CTGCCCACAGAGAGG[-/T]TTTTTTTTTTTGTTT	57674
rs57423401	snp	A/T	0.171057	0.237209	intron-variant	RNF213	GRCh38.p7	17:80342773	ATATTATATATATAT[A/T]TTTTTTGAGACAGAG	57674
rs57442349	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80324437	AATTACACTTGATCG[A/T]GGTGTATAGTTCCTT	57674
rs57480819	in-del	-/G/GG	0	0	intron-variant	RNF213	GRCh38.p7	17:80323843	TTTTTTGGGGGGGGG[-/G/GG]TGCTATTGTAATTGG	57674
rs57500794	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80331405	CTTTTTTTTTTTTTT[-/TT]GATATGGAGTCTCAC	57674
rs57535730	snp	G/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80323835	TAAGTACTTTTTTTT[G/T]GGGGGGGGTGCTATT	57674
rs57689017	snp	A/T	0.0260105	0.111035	intron-variant	RNF213	GRCh38.p7	17:80271285	AGACGTTTAGAGGAT[A/T]TGTTATCAATTTTGA	57674
rs57789415	in-del	-/GTCT			intron-variant	RNF213	GRCh38.p7	17:80268645	TCCATCCGTTTATCT[-/GTCT]ATCTATCTGTCATCT	57674
rs57805445	snp	C/T	0.0414363	0.137845	intron-variant	RNF213	GRCh38.p7	17:80302008	GCTTGGAGGAGATTA[C/T]GTTAAGTGAAATAAG	57674
rs57961685	snp	A/G	0.444444	0.157135	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355542	GGAAGAAGCGGGGTG[A/G]ACGGGAATGGGGGCT	57674
rs57970281	snp	A/C/G	0.00358891	0.0422285	intron-variant	RNF213	GRCh38.p7	17:80312384	GTCCGGCACGGAGGC[A/C/G]GGGGGAGAGCATGAT	57674
rs58124977	snp	C/G	0.443598	0.158176	intron-variant	RNF213	GRCh38.p7	17:80331644	TCCGCCCATCTCAGC[C/G]TCCCAACGTGCTGGG	57674
rs58201003	snp	A/G	0.107694	0.205546	intron-variant	RNF213	GRCh38.p7	17:80297437	CCTGGGCGACACAGT[A/G]AGACTTCATCTCAAA	57674
rs58228329	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80315840	GGTGATGGTGATGGT[G/T]GTGGTGGTGGTGGTG	57674
rs58281950	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80322152	GCCCCTCATCCCCCC[-/C]ACCCCCCCTTTTTTT	57674
rs58313556	in-del	-/A	0.474091	0.11083	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375542	AAAGAAAAAAAAAAA[-/A]GAATTAGCCGGACAT	57674
rs58364615	snp	G/T	0.00779006	0.0619221	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386302	CTTGGATCTGGACAC[G/T]GAGTTTGAGATCCTC	57674
rs58464628	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80308557	TAAGGCTCCTCCTAA[A/G]TCCCTGCTCTGTCCA	57674
rs58499055	snp	G/T	0.0193772	0.0965046	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375462	ATCCTAGCACTTTGG[G/T]AGGCCGAGGCATGCA	57674
rs58617429	snp	C/T	0.498927	0.0231381	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358939	AAGTTTACGAAGCTC[C/T]GAGAAATTTCTGTTT	57674
rs58647907	snp	A/C	0.181022	0.240296	intron-variant	RNF213	GRCh38.p7	17:80271731	AGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA	57674
rs58724575	snp	A/C/T	0.0670745	0.170406	intron-variant	RNF213	GRCh38.p7	17:80285346	CAGGCCCTCTAAACC[A/C/T]AGCCCAGACGCCACT	57674
rs58826434	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80307381	TTTTTTTTTTTTTTT[-/TT]GAGTCAGAGTCTTAC	57674
rs58837749	in-del	-/ATG			intron-variant	RNF213	GRCh38.p7	17:80313760	CTGGTGGTGGAGGTG[-/ATG]GTGGAGGTACTGGAG	57674
rs58866280	in-del	-/CCC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396744	CCCCCACCCCCCCCC[-/CCC]AACCAGAGCAACTTT	57674
rs58875496	snp	A/C			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396274	CTCAAAAAAAAATAA[A/C]ATAAGGACCTTATTG	57674
rs58925434	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80277431	GGGGAAACCCCGTCT[C/T]TACTAAAAATACAAA	57674
rs59096304	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313791	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs59109577	snp	A/G	0.0298908	0.118541	intron-variant	RNF213	GRCh38.p7	17:80330500	GAGAAGCGGGCTGGC[A/G]GGCCTTGGCATCCCG	57674
rs59110729	snp	C/T	0.161267	0.233723	intron-variant	RNF213	GRCh38.p7	17:80277800	TGCTCTAAGCGCAGA[C/T]GCCGCATTCTAACCA	57674
rs59209118	snp	G/T	0.091768	0.193553	intron-variant	RNF213	GRCh38.p7	17:80290747	AGCGTGTCTGTAGGC[G/T]TGGGAGGAATCCCTC	57674
rs59237306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80313722	GTGATGGAGGTGGTG[A/G]TGGTGGAGGTGACAA	57674
rs59301720	snp	G/T	0.0535932	0.154675	intron-variant	RNF213	GRCh38.p7	17:80318282	AGAGTAGGCACACGG[G/T]GATAGAGGTTCTCAC	57674
rs59352873	in-del	-/TTTTT			intron-variant	RNF213	GRCh38.p7	17:80307872	TTTTTTTTTTTTTTT[-/TTTTT]AAAGGGAAATAATAG	57674
rs59370180	snp	A/G	0.02016	0.0983543	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390831	ACTTTGGGAGGCCGA[A/G]GTGGGTGGATCACCT	57674
rs59452568	snp	A/T	0.378765	0.214288	intron-variant	RNF213	GRCh38.p7	17:80293065	TAAACATATATATAT[A/T]TTTTTTTTCTGAGAC	57674
rs59498373	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387299	TTGGTAGAGATGGGG[-/G]CTTCACCACGTTGCC	57674
rs59627017	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80313848	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs59640970	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354692	TGTTTCTTTCCAAAC[A/C]TCTCAGCCATTCAAA	57674
rs59796511	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268627	CATCCATCCATCCAT[C/T]CATCCATCCGTTTAT	57674
rs59864587	snp	C/T	0.127944	0.218179	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352329	GGAGGCTGCGTGCAC[C/T]TCTCCTGGACTGACT	57674
rs59888214	snp	C/G	0.0763149	0.179815	intron-variant	RNF213	GRCh38.p7	17:80298866	TGCTTGTAATCCCAG[C/G]TACTCTGGAGGCTGA	57674
rs59917309	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80313746	GTGACAATGGTGATG[C/G]TGGTGGTGGAGGTGG	57674
rs60020928	in-del	-/G/GG/TGGG	0.352287	0.228117	intron-variant	RNF213	GRCh38.p7	17:80323834	TAAGTACTTTTTTTT[-/G/GG/TGGG]GGGGGGGGGTGCTAT	57674
rs60077702	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80313869	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs60117041	in-del	-/A	0.482234	0.0925596	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367132	AGGTATCATGAAGAG[-/A]ATGAGTTGCAGAAGC	57674
rs60209216	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80322161	CCCCCCCACCCCCCC[-/T]TTTTTTTTTTTTTTT	57674
rs60321521	in-del	-/A	0.478354	0.101757	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399127	AGGAAAAAAAAAAAA[-/A]GGATGATTTAACTTT	57674
rs60333843	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80338973	TAAAAAAAAAAAAAA[-/A]TTAAAACAAATGATA	57674
rs60373273	snp	G/T	0.373799	0.217195	intron-variant	RNF213	GRCh38.p7	17:80307858	CCTGGCCGTCTGTTT[G/T]TTTTTTTTTTTTTTT	57674
rs60388544	snp	G/T	0.162909	0.23434	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320345	GTTTTTTTGTTGTTG[G/T]TGGTGGTGGTTGTTT	57674
rs60430048	snp	C/T	0.168135	0.236216	intron-variant	RNF213	GRCh38.p7	17:80342612	TATATATATTCGATA[C/T]ATATTCTATATAGAT	57674
rs60571269	snp	C/T	0.0189856	0.0955633	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353951	GACCCTCATCGCATA[C/T]GGGCGGTTTGGCTTT	57674
rs60622250	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312392	CGGAGGCGGGGGGAG[A/G]GCATGATGGGAGCAC	57674
rs60733836	snp	A/G	0.0267878	0.112589	intron-variant	RNF213	GRCh38.p7	17:80263322	TCAGGGCAGGCCGTG[A/G]GACCCTGCCGAACAG	57674
rs60753852	snp	A/C/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313809	GTGATGGTGGAGGTA[A/C/G]TGGAGGTGATGGTGG	57674
rs60777731	in-del	-/A	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366669	AGGATGGCTCAAAAT[-/A]AAAAAAAAAAAATCT	57674
rs60826056	snp	C/T	0.0219119	0.102351	synonymous-codon	RNF213	GRCh38.p7	17:80273365	TTGGCAAGAAAACCC[C/T]GAGGAGCCCTGTTCC	57674
rs60966402	snp	C/G	0.347694	0.230122	intron-variant	RNF213	GRCh38.p7	17:80269037	CAAAGAACCTGAAGT[C/G]TGATGTCCAAGGGCA	57674
rs61043311	in-del	-/CC			intron-variant	RNF213	GRCh38.p7	17:80268635	CATCCATCCATCCAT[-/CC]GTTTATCTGTCTATC	57674
rs61055659	snp	A/G	0.0539704	0.155153	intron-variant	RNF213	GRCh38.p7	17:80318065	TCAGGACGTCTTTCC[A/G]AAGTTAAACCGTCTC	57674
rs61087724	snp	G/T	0.481242	0.0950111	intron-variant	RNF213	GRCh38.p7	17:80307288	GGCCGTGACCCACAT[G/T]TGCTGTTGTAACAGC	57674
rs61118700	snp	C/T	0.44333	0.158505	intron-variant	RNF213	GRCh38.p7	17:80308234	TGTTCACGTCTCTGC[C/T]GATGTTGATCCAGCA	57674
rs61152002	in-del	-/TGTTAAGATAATGACTG/TGTTAAGATAATGATTG	0.477747	0.24156	intron-variant	RNF213	GRCh38.p7	17:80299217	AATTCTTGTCTATGT[lengthTooLong]CTTAGCGTTCCAGCC	57674
rs61222564	snp	G/T	0.468349	0.121752	intron-variant	RNF213	GRCh38.p7	17:80307860	TGGCCGTCTGTTTTT[G/T]TTTTTTTTTTTTTTT	57674
rs61256971	snp	C/T	0.0755793	0.179102	intron-variant	RNF213	GRCh38.p7	17:80299192	TTTGTGAACCATTTT[C/T]TCCATCAGCAAATTC	57674
rs61327219	snp	A/G	0.441977	0.16014	intron-variant	RNF213	GRCh38.p7	17:80308226	ACCTCCTTTGTTCAC[A/G]TCTCTGCCGATGTTG	57674
rs61359568	snp	A/G	0.0919652	0.193714	missense	RNF213	GRCh38.p7	17:80325126	TCCTGGCCTAGGACC[A/G]CGGACAACTTCAATG	57674
rs61407399	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80268639	CATCCATCCATCCGT[C/T]TATCTGTCTATCTAT	57674
rs61429875	snp	A/C	0.0381685	0.132768	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393425	CTCAGTTCCCAGAAG[A/C]GATACTGCTCGCCAG	57674
rs61511127	in-del	-/CAAAA			intron-variant	RNF213	GRCh38.p7	17:80284394	AAAAACAAAACAAAA[-/CAAAA]ATAGCTGGGCGTGGT	57674
rs61541764	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268628	ATCCATCCATCCATC[C/T]ATCCATCCGTTTATC	57674
rs61546164	in-del	-/T	0.266819	0.249434	intron-variant	RNF213	GRCh38.p7	17:80303568	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	57674
rs61557840	snp	C/G	0.0452528	0.143452	intron-variant	RNF213	GRCh38.p7	17:80279360	GCCTGAACACAAGGT[C/G]TTGGATGGCGCTCGC	57674
rs61576092	in-del	-/C			frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372732	GCCTGAGGGAGGCCC[-/C]AGGCAAGTCTTCTCT	57674
rs61600413	snp	C/T	0.104037	0.202965	missense	RNF213	GRCh38.p7	17:80347357	TTGCCCGAGGCCAAG[C/T]GCTCAGAGGAAGTCA	57674
rs61644336	snp	C/T	0.253264	0.249979	intron-variant	RNF213	GRCh38.p7	17:80292633	GACGCGGGCGCTTCC[C/T]TTCTCGCAGAGCCCT	57674
rs61673418	snp	A/G	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80342327	CTAGTGCTAAGTGGC[A/G]CGGGACTCTGCTTTG	57674
rs61721293	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313915	TGGTGGTGGTGGTGA[A/T]GGTGGAGGTGGTGGA	57674
rs61724379	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80313935	GAGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs61729879	snp	C/T	0.00879075	0.0657122	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376423	GGCGGGGCCTAGTGA[C/T]AGCAACCTTGATGGA	57674
rs61732734	snp	A/G	0.000115303	0.00759199	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376356	TCCTTTCACCTCCTG[A/G]TATCAGCCGTTTTGC	57674
rs61739536	snp	A/G	0.0099513	0.0698328	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379664	CATTGACTGCCATGC[A/G]CCGATTGGAGGCATT	57674
rs61740658	snp	A/G	0.155257	0.231352	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363784	AGGCTGTCATCAGGG[A/G]AGTCAGGTGAGACCC	57674
rs61741791	snp	A/G	0.0942179	0.19553	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361810	GCTCCATGGAGAGCC[A/G]CAGCAGGAACTTCTT	57674
rs61741961	snp	G/T	0.0197642	0.0974243	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383030	AAATGAGGAACAACT[G/T]GGAAAAGGAAATCGC	57674
rs61743307	snp	A/G	0.000428343	0.0146283	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374465	TATTCCAGGGGCTGC[A/G]GCAGGACCACCCAGG	57674
rs61744736	snp	C/G	0.00136638	0.0261021	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383793	CTTCCTGCCCCACCT[C/G]CCCCGGAAAAGTGTG	57674
rs61745567	snp	A/C/G	0.000625842	0.0176793	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389247	TGCCTGTGAAGTGCT[A/C/G]TCTGTCGTAGAAGTC	57674
rs61745599	snp	C/G	0.124974	0.216491	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381694	CTCGTCCTGCGCAGG[C/G]TTCTCCAAGAGCAGC	57674
rs61745927	snp	C/T	0.00342189	0.0412218	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393435	AGAAGAGATACTGCT[C/T]GCCAGCTGTGTCTCA	57674
rs61746605	snp	C/G	0.0041759	0.0455029	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385158	CAGAGGCTTCCTCAG[C/G]AAGCACAGCTCAGGT	57674
rs61747138	snp	C/T	0.0132431	0.0802882	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380956	TACTCACTCACTTGG[C/T]TCTGCTTCTGGGAGC	57674
rs62074441	snp	C/T	0.487558	0.0778863	intron-variant	RNF213	GRCh38.p7	17:80262637	CCTTTTACAAAAGGA[C/T]AGCTTCCCAGAACTC	57674
rs62074443	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80268641	TCCATCCATCCGTTT[A/G]TCTGTCTATCTATCT	57674
rs62074444	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80268645	TCCATCCGTTTATCT[A/G]TCTATCTATCTGTCA	57674
rs62074445	snp	C/T	0.169435	0.236663	intron-variant	RNF213	GRCh38.p7	17:80277897	AGCCTCACCCTGCAG[C/T]AGAGTCAGGTGGTCA	57674
rs62076476	snp	C/G	0.294532	0.246002	intron-variant	RNF213	GRCh38.p7	17:80289630	GTGGAGGCCGGCCTT[C/G]AAGGTCAGGGTTTGG	57674
rs62076479	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291104	GGCATGAGCCACTGC[A/G]CCCAGCCTTTAAATA	57674
rs62076480	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80292450	GAGGGGCAGCAAAGG[A/C]CTGGGAGCTGGGTCA	57674
rs62076483	snp	A/G	0.0923359	0.194016	intron-variant	RNF213	GRCh38.p7	17:80297680	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	57674
rs62076484	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80302620	CAGTACTTTGGGAGG[A/C]CCAGGCAGGAGGATT	57674
rs62076485	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80306669	ATCCTGGCTAACACA[G/T]TGAAACCCCGTCTCT	57674
rs62076487	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313504	GGTTGGTGGTGGTGG[A/T]GGTAGAGGTGATGGT	57674
rs62076488	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313515	GTGGTGGTAGAGGTG[A/G]TGGTGGTGAAGGTGA	57674
rs62076489	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313521	GTAGAGGTGATGGTG[A/G]TGAAGGTGATGGTGA	57674
rs62076490	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80313529	GATGGTGGTGAAGGT[C/G]ATGGTGATGGTGGAC	57674
rs62076491	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313534	TGGTGAAGGTGATGG[A/T]GATGGTGGACGTAAT	57674
rs62076492	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313536	GTGAAGGTGATGGTG[A/G]TGGTGGACGTAATGG	57674
rs62076493	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80313544	GATGGTGATGGTGGA[C/G]GTAATGGAGGTGATG	57674
rs62076494	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313547	GGTGATGGTGGACGT[A/G]ATGGAGGTGATGGTG	57674
rs62076495	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313552	TGGTGGACGTAATGG[A/T]GGTGATGGTGGTGAT	57674
rs62076496	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313557	GACGTAATGGAGGTG[A/G]TGGTGGTGATGGTGG	57674
rs62076497	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313561	TAATGGAGGTGATGG[A/T]GGTGATGGTGGTCAT	57674
rs62076499	snp	A/G	0.0693013	0.172766	intron-variant	RNF213	GRCh38.p7	17:80323702	TCAGATGATCAACCC[A/G]CCTTGACCTCCCAGA	57674
rs62076521	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80343388	GTCCCCATGTCTCTG[C/T]GTGACTCCTCCCCGT	57674
rs62076525	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355412	ATGGGAATGGGGGCT[C/T]ACGGAGGAAGAAGCG	57674
rs62076526	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355415	GGAATGGGGGCTCAC[A/G]GAGGAAGAAGCGGGG	57674
rs62076527	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355417	AATGGGGGCTCACGG[A/G]GGAAGAAGCGGGGTG	57674
rs62076528	snp	A/G	0.481165	0.0951993	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356956	CAGAGTCTCACTCTC[A/G]TCCCCCATGCTGGAG	57674
rs62076531	snp	A/T	0.0670745	0.170406	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366035	CACAGCCAAAGACCT[A/T]ACCTCGTTAGTTTTC	57674
rs62077763	snp	C/T	0.0603597	0.1629	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370413	GAGGTTAAAACTATT[C/T]TAAAAATTAGATTAC	57674
rs62077764	snp	A/C	0.0875214	0.190002	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373070	TACCTGGTGCGGAAG[A/C]TCAGCAGCCAGCGGG	57674
rs62077765	snp	A/G	0.0629771	0.165899	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377706	AGCTTTCCCTTTTCA[A/G]TGTGGGTCATTGGGT	57674
rs62077766	snp	A/G	0.0766824	0.180169	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382151	CCATCACAGTTGTGT[A/G]CTGATTTATTAAATG	57674
rs62077767	snp	A/G	0.021333	0.101051	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384563	AGTTGAGGAGTATGA[A/G]TTCACAATGACAGGA	57674
rs62077768	snp	C/T	0.130427	0.219554	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385509	GGGGTTGCTATCATA[C/T]GGTTCTTACCAAGTA	57674
rs62077769	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386975	TTCTCGAGAGAGGGA[A/G]GCAGCACCTCACCCT	57674
rs62077770	snp	C/G	0.0777841	0.181223	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387624	GGTTCTTCAGTCCAC[C/G]GCCTAAAACCCACAT	57674
rs62635847	snp	C/T	0.479014	0.100263	intron-variant	RNF213	GRCh38.p7	17:80281254	ACACCTCAACACACA[C/T]ACCCCACTCACACCA	57674
rs62647784	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80313887	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs62647785	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313948	TAATGGAGGTGATGG[A/T]GGTGGTGGAGGTGAT	57674
rs62647786	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313953	GAGGTGATGGTGGTG[A/G]TGGAGGTGATGGTGG	57674
rs62647787	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313957	TGATGGTGGTGGTGG[A/T]GGTGATGGTGGAGGT	57674
rs62647788	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313962	GTGGTGGTGGAGGTG[A/G]TGGTGGAGGTACTGG	57674
rs62647789	snp	A/C/G			intron-variant	RNF213	GRCh38.p7	17:80314868	GTGGTGGTGGAGGTA[A/C/G]TGGAGGTGATGGTGG	57674
rs62647790	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80314963	GGAGGTGATGGTGGT[C/G]GTGTAGGTGATGGTG	57674
rs62647791	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315543	GAGGTACTGGAGGTG[A/G]TGGTGGTCGTGGAGG	57674
rs62648776	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315582	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs62648777	snp	C/T	0.499527	0.0153681	intron-variant	RNF213	GRCh38.p7	17:80315737	AGGTACTGGAGGTGA[C/T]GGTGGTGGTGGTGGA	57674
rs62650597	in-del	-/AGGTGATGG			intron-variant	RNF213	GRCh38.p7	17:80313957	TGATGGTGGTGGTGG[-/AGGTGATGG]TGGAGGTACTGGAGG	57674
rs62650598	in-del	-/GG			intron-variant	RNF213	GRCh38.p7	17:80313922	GGTGGTGATGGTGGA[-/GG]TGGTGGAGGTAATGG	57674
rs62650599	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80313920	GTGGTGGTGATGGTG[-/G]AGGTGGTGGAGGTAA	57674
rs62650600	in-del	-/GTGGTG			intron-variant	RNF213	GRCh38.p7	17:80313908	GTGATGGTGGTGGTG[-/GTGGTG]ATGGTGGAGGTGGTG	57674
rs66638970	in-del	-/TTCT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365437	GGTGCCCACGCTCCG[-/TTCT]TCTTGTCCCTTCATT	57674
rs66667664	in-del	-/TGTTAAGATAATGACTG			intron-variant	RNF213	GRCh38.p7	17:80299218	ATTCTTGTCTATGTC[-/TGTTAAGATAATGACTG]TTAGCGTTCCAGCCA	57674
rs67070144	in-del	-/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80306868	ACATGAGACGCCTTC[-/T]TTTTTTTTTTTTTTT	57674
rs67189003	snp	A/G	0.245346	0.249957	intron-variant	RNF213	GRCh38.p7	17:80262600	CCATTCTGCTGTTTC[A/G]TGGTGTGGATTTCCT	57674
rs67262798	snp	C/T	0.16846	0.236329	intron-variant	RNF213	GRCh38.p7	17:80340560	GGTATTCCCTGGGAG[C/T]CCCATTCCCTTCCTC	57674
rs67516934	in-del	-/CACAGTGCTGGGCTTACACACGTGAGCCA	0.202035	0.245356	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393240	CCCACCTCAGCCTCC[lengthTooLong]CACAGTGCTGGGCTT	57674
rs67535549	in-del	-/TGGTGGGAGGGTAGGT	0.499998	0.000998401	intron-variant	RNF213	GRCh38.p7	17:80271097	GTCAGGGCCCGCCCC[-/TGGTGGGAGGGTAGGT]TGGTGGGAGGGTAGG	57674
rs67960446	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80325678	CTGTCTGATTTCCCC[-/A]CCAGCCCCCCGCGCC	57674
rs67982382	snp	G/T	0.457504	0.139435	intron-variant	RNF213	GRCh38.p7	17:80277685	GTGAATGCCGATGGG[G/T]TGTCTCTGGTGATGA	57674
rs71163942	in-del	-/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80267126	GGGTTCAAGCAATTC[-/C]TTGTGCCTCAGCCTC	57674
rs71163943	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80267824	CCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGA	57674
rs71163947	in-del	-/A/TT	0	0	intron-variant	RNF213	GRCh38.p7	17:80289608	GGCCTCCACATTTTC[-/A/TT]TTTTTTTTTTTTTTT	57674
rs71163948	in-del	-/TCTCCTGCCTCAG	0	0	intron-variant	RNF213	GRCh38.p7	17:80304539	CCAGGCTCACGCCAT[-/TCTCCTGCCTCAG]CCTCCCCAGTAGCTG	57674
rs71163949	in-del	-/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80304661	TAATTATTATTATTA[-/T]TTATTTATTTATTTA	57674
rs71163950	in-del	-/AAAAA	0	0	intron-variant	RNF213	GRCh38.p7	17:80305197	GACCAAAACTGTCTC[-/AAAAA]AAAAAAAAAAAAAGT	57674
rs71163953	in-del	-/TTATG	0	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396278	CACACAATAAGGTCC[-/TTATG]TTATTTTATTTTTTT	57674
rs71163954	in-del	-/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396733	TTGCGGGGGGGGGGT[-/G]GGGGGGGAAATGCAC	57674
rs71281352	in-del	AAAC/CAAACAA	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80265042	AAAAAAAAAAAAAAA[AAAC/CAAACAA]AAACAAACATGGAAG	57674
rs71354803	in-del	CCCTG/TCCA	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355522	CACCCCGCTTCTTCC[CCCTG/TCCA]TAAGCCCCCATTCCC	57674
rs71354804	multinucleotide-polymorphism	GT/TC	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355504	AAGCCCCCATTCCCG[GT/TC]CACCCCGCTTCTTCC	57674
rs71354805	in-del	CCCTGTA/TCTGTG	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355483	CACCCCGCTTCTTCC[CCCTGTA/TCTGTG]AGCCCCCATTCCCGG	57674
rs71354806	multinucleotide-polymorphism	CATTCCCG/GATTCCCA	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355435	TCCTCCGTGAGCCCC[CATTCCCG/GATTCCCA]TCCACCCCGCTTCTT	57674
rs71354807	in-del	ACCG/CCA	0.5	0	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287177	TAGAGGCAGAGTCTC[ACCG/CCA]TGTTGCTCAGGCTGG	57674
rs71354808	multinucleotide-polymorphism	AGCAACACCGC/GGAAACACCGT	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80282246	ACAAAGAACACAAAG[AGCAACACCGC/GGAAACACCGT]ACCGTGTAGCAACTG	57674
rs71365597	in-del	-/TG	0.375	0.216506	intron-variant	RNF213	GRCh38.p7	17:80290415	GTGTGTGCGTGTGTG[-/TG]CGAGTGTGCGCGTGT	57674
rs71365598	in-del	-/A	0.399432	0.200425	intron-variant	RNF213	GRCh38.p7	17:80298812	TGTACGAAAAATACC[-/A]AAAAAAAAAAAAAAA	57674
rs71365599	in-del	-/T	0.457013	0.140162	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356008	GGACTCTCTTGATGC[-/T]TTTTTTTTTTTGAGA	57674
rs71365601	in-del	-/GA	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397385	CTGCCTCCAAAGAGA[-/GA]AGTAAAAACTAAAAG	57674
rs71368066	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80315830	AGGTGATGGTGGTGA[A/T]GGTGATGGTTGTGGA	57674
rs71369100	multinucleotide-polymorphism	CCTGTAAGCCCCCATTCCCACTCACCCCG/TCCATAAGCCCCCAATCCTGTTCACCCCA	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355637	CACCCCGCTTCTTCC[lengthTooLong]CTTCTTCCCCTGTGA	57674
rs71369101	in-del	CACTCACCC/TGGTCACCCCACTTCTTCGT	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355574	GTGAGCCCCCATTCC[CACTCACCC/TGGTCACCCCACTTCTTCGT]CGCTTCTTCCTCCAT	57674
rs71369102	multinucleotide-polymorphism	ATT/GTC	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355542	TAAGCCCCCATTCCC[ATT/GTC]CACCCCGCTTCTTCC	57674
rs71389747	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80277264	GAGGAGTGGGGAGGA[A/G]GGAGTCATTGCTGTG	57674
rs71389748	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80277531	TGAACCTAGGAGGCA[A/G]AGGTTGCAGTGAGCC	57674
rs71389749	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80310107	TTCTGCCTCCGACTT[C/T]CCCCACTCACCCCCA	57674
rs71389750	snp	G/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80312106	GTACTCCAGCCTGGG[G/T]TACAGAGTGAGACTC	57674
rs71389751	snp	C/T	0.346368	0.23068	intron-variant	RNF213	GRCh38.p7	17:80316292	TTTCATGTGTTTCAA[C/T]CTCCTAGTGTCCCTG	57674
rs71389752	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355595	GTGGGAATGGGGGCT[C/T]ACAGGGGAAGAAGTG	57674
rs71389753	snp	C/T	0.0696718	0.173152	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388441	TTCCCGGTTGTGTTA[C/T]TATTTCCATAGATGG	57674
rs71852986	in-del	-/GTAGAGGACAGGCCGTTTTCCTTAAGAG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365519	CAGAAAGCAGGGGAG[-/GTAGAGGACAGGCCGTTTTCCTTAAGAG]CCCAATCCCGGACAC	57674
rs71876001	in-del	-/T	0.498871	0.0237351	intron-variant	RNF213	GRCh38.p7	17:80273614	GGGGCCTCCACCGTC[-/T]TTTTTTTTTTTTTTT	57674
rs72287573	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80274648	GGGGGTGTGGGGTGA[-/GT]GTGTGGGGTGAGTGG	57674
rs72359531	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80265044	TTCCATGTTTGTTTG[-/T]TTTTTTTTTTTTTTT	57674
rs72532137	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80325676	TGCTGTCTGATTTCC[-/A]CCCCAGCCCCCCGCG	57674
rs72847090	snp	G/T	0.0170251	0.090679	intron-variant	RNF213	GRCh38.p7	17:80270104	CTCCTCTGCGTGAAT[G/T]TGTGCGCACACACAC	57674
rs72847093	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80272397	GTCTGGTGAGGGCTT[C/T]TGTGCCACATGGCAG	57674
rs72847097	snp	C/T	0.405082	0.196086	intron-variant	RNF213	GRCh38.p7	17:80274570	GGGAAGTGATGCAGC[C/T]GCAGTGCTGTGGTCT	57674
rs72849808	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80280899	CACGGAGTAACAGAG[A/G]CGCGACCTGGGGATG	57674
rs72849822	snp	A/G	0.2776	0.248472	intron-variant	RNF213	GRCh38.p7	17:80289016	ACAGCCCGAGTGGCC[A/G]GGCGAGGCCTCTCTT	57674
rs72849837	snp	C/G	0.0232809	0.105349	missense	RNF213	GRCh38.p7	17:80298430	GAGCTGGCCCCGCGG[C/G]ACAAGGATGCCTGGA	57674
rs72849841	snp	C/T	0.217263	0.247847	missense	RNF213	GRCh38.p7	17:80298494	GACTCTCCTTCTCAC[C/T]GTTCCGGGAACAAAT	57674
rs72849844	snp	C/T	0.132409	0.220618	intron-variant	RNF213	GRCh38.p7	17:80299810	ACAAGTGAGAACCTG[C/T]GGTATTTGGTTCTCG	57674
rs72849848	snp	A/G	0.132751	0.2208	intron-variant	RNF213	GRCh38.p7	17:80301356	GCTTCTGTGCAGCAA[A/G]GGAAACTATCAACAG	57674
rs72849849	snp	A/G	0.0810805	0.184299	intron-variant	RNF213	GRCh38.p7	17:80301640	TCAAAAAGACAAAAA[A/G]TAAATGCCAGTGAGG	57674
rs72849850	snp	C/T	0.148661	0.22854	intron-variant	RNF213	GRCh38.p7	17:80304863	CATCCCCATGAAACA[C/T]GACCTCCACACTCCC	57674
rs72849865	snp	A/G	0.00996817	0.0698908	synonymous-codon	RNF213	GRCh38.p7	17:80317214	GCTGGTGGAAATCCA[A/G]TTCCCCGCGGAGCAT	57674
rs72849868	snp	C/T	0.0422008	0.138995	intron-variant	RNF213	GRCh38.p7	17:80317709	GGTGCCTGCAACCCC[C/T]GAAGCTCCAGAGGGC	57674
rs72849894	snp	C/T	0.0520825	0.152737	intron-variant	RNF213	GRCh38.p7	17:80329960	TTCTCTTGCTGGAAT[C/T]CCTGTTAATTGGATA	57674
rs72851440	snp	A/G	0.0532157	0.154195	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356298	TGAGCCAGTGTGCCC[A/G]GCCTGTTGATGCTTT	57674
rs72851455	snp	A/G	0.046775	0.145601	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363545	ATGCAGCTAACAGCC[A/G]GGGCCTCTGGTGGGC	57674
rs72851458	snp	A/G	0.0463947	0.145069	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363884	TGAGAAGACGGGCAG[A/G]TGCTCCTGCCATGGG	57674
rs72851471	snp	A/C	0.0444908	0.142359	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368261	AAAACCTGACCTCAG[A/C]GAACTATCATAAGAG	57674
rs72851475	snp	C/T	0.0456336	0.143994	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374345	TCAGGGAATCCCAGC[C/T]TGGCTGCCTTTAAAC	57674
rs72851478	snp	C/T	0.180702	0.240204	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378724	TCCATGAAATGAGGA[C/T]GCTGAAATAGAGTCT	57674
rs72851480	snp	C/T	0.0626037	0.165477	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381179	TGGGGGGAACTACTC[C/T]CCAGATTATACAGAA	57674
rs72851489	snp	G/T	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384135	CGTAAAGTCACAGAC[G/T]AAATACACACCCACG	57674
rs72851492	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384248	AGCTCTTTCCCAGCC[A/G]CTCTGTTCCTCTCTG	57674
rs72851497	snp	A/T	0.308414	0.24308	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392095	TCTTGTGCTTTCACA[A/T]ACTTGTTTTATTCAC	57674
rs72851498	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394310	CTGGCAGTTCTTTGC[C/G]GACTTTTTTCTAGCA	57674
rs73432189	snp	A/G	0.0252325	0.109451	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261308	TGCGCCTGTACGAAT[A/G]GCAACAACGGAAAAG	57674
rs73432984	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320254	GCTTCTGTGGCTTTC[C/T]CTGTTCTGACTGTCA	57674
rs73434820	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80335221	AGGCGTGAGCCACCG[C/T]GCCTGGCCCCACAGA	57674
rs73440489	snp	A/T	0.0345262	0.126772	intron-variant	RNF213	GRCh38.p7	17:80261733	ACAATAAGATGCTTT[A/T]GGGGGCCGGGCGCAG	57674
rs73440495	snp	A/G	0.046775	0.145601	intron-variant	RNF213	GRCh38.p7	17:80262090	AGAAGGAAACACTTC[A/G]GGTGGAAAGAAAGAG	57674
rs73440734	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80349120	GGGGGTGGAGGGGTC[C/T]GGGGCGACCCCCTGG	57674
rs73440754	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353885	AGGGCGGAGGTCGGC[A/G]TCTCTTCTTTGTCCG	57674
rs73442404	snp	C/T	0.123798	0.215808	intron-variant	RNF213	GRCh38.p7	17:80264614	CCATCACCCCGGGGC[C/T]CTCTCCTTCCTCCAT	57674
rs73442406	snp	A/C	0.216649	0.247765	intron-variant	RNF213	GRCh38.p7	17:80264631	TCTCCTTCCTCCATG[A/C]CCCACATGCAGAGGG	57674
rs73442408	snp	C/T	0.26271	0.249677	intron-variant	RNF213	GRCh38.p7	17:80267209	GTGACAACAGCGAGA[C/T]TCTGTCTCAAAAAAA	57674
rs73442415	snp	C/T	0.144632	0.226711	intron-variant	RNF213	GRCh38.p7	17:80269490	TTCTATCTATCCATC[C/T]ATCCATTCATCTATT	57674
rs73442418	snp	C/G	0.0221141	0.102801	intron-variant	RNF213	GRCh38.p7	17:80269673	ATCTATCCATCCATC[C/G]ATTCATCTGTTCTAT	57674
rs73442420	snp	A/T	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80272578	AGCCATTCGTGAGGG[A/T]TTTGCCCTCACGACC	57674
rs73442421	snp	C/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80272860	GGGAGAATGCCCACC[C/G]TGGGGAAGACAGGAG	57674
rs73442428	snp	A/G	0.0221141	0.102801	intron-variant	RNF213	GRCh38.p7	17:80274087	TGCTTCGGGGCAGGG[A/G]CCTGAGCGTCCGCTG	57674
rs73442431	snp	C/T	0.0984431	0.198823	intron-variant	RNF213	GRCh38.p7	17:80274111	TCCGCTGGGTGCGTG[C/T]CTTGCGCTTCTGTAG	57674
rs73442432	snp	C/T	0.122064	0.214785	intron-variant	RNF213	GRCh38.p7	17:80274116	TGGGTGCGTGTCTTG[C/T]GCTTCTGTAGGCCTC	57674
rs73442434	snp	C/T	0.0984431	0.198823	intron-variant	RNF213	GRCh38.p7	17:80274273	TGGCCTTGAACAGCC[C/T]CTTAGGCGTTAGACA	57674
rs73442436	snp	A/G	0.0225045	0.103662	intron-variant	RNF213	GRCh38.p7	17:80274410	CCTGGGCTCTAGCGC[A/G]GCCTGGGAAGACCCA	57674
rs73442437	snp	A/G	0.0984431	0.198823	intron-variant	RNF213	GRCh38.p7	17:80274428	CTGGGAAGACCCAGA[A/G]GGCAGTGTCAGCTCC	57674
rs73442751	snp	A/C	0.128632	0.218563	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389745	AGAATGCCTGTGTGG[A/C]GAGCACTCAGGCTCC	57674
rs73442756	snp	C/T	0.0486741	0.148216	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394714	CAGGACTCAGCCATG[C/T]ACACCTTGAGCAGCG	57674
rs73442758	snp	C/T	0.129664	0.219133	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396154	GTAATCCCAGCTACC[C/T]GGGAGGCTGAGGTAT	57674
rs73444311	snp	A/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80278250	GCGATGCCCGGTGTG[A/G]TGTGGAAGGGAGGTG	57674
rs73444313	snp	C/T	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80278546	TGGACTTGTCCTGCA[C/T]GTCTGCAGGAGCTGC	57674
rs73444315	snp	A/G	0.0260105	0.111035	intron-variant	RNF213	GRCh38.p7	17:80279262	TCCACCAGCAACACA[A/G]GCTTCACCACAGAGA	57674
rs73444339	snp	A/G	0.342582	0.232225	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287484	TCCATCCTGGGCGAC[A/G]GAGGGAGACCTTGTC	57674
rs73444349	snp	A/G	0.105214	0.203807	intron-variant	RNF213	GRCh38.p7	17:80292902	CCCCTGGTGTCCGGT[A/G]TCTTGGAAACAGTTG	57674
rs73444352	snp	A/G	0.030278	0.119257	intron-variant	RNF213	GRCh38.p7	17:80293341	TGCTGGGATTAAGAC[A/G]TGAGCCACTGTGCCC	57674
rs73446338	snp	A/T	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80302889	CAAACTTTCTCTTTA[A/T]GTATAATCTCTCTGA	57674
rs73446358	snp	A/C	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80310046	GCTTAAACCACCACG[A/C]CCAGCCTCCCATGGA	57674
rs73446366	snp	A/G	0.0558544	0.157504	intron-variant	RNF213	GRCh38.p7	17:80311257	AAAAATACGTGACGC[A/G]TGTTGAAGAAACTTT	57674
rs73446376	snp	A/G	0.0528381	0.153711	intron-variant	RNF213	GRCh38.p7	17:80316109	TTTTCATTTTTGGCT[A/G]GGCACTATGGCTGAT	57674
rs74000503	snp	A/T	0.00676609	0.0577691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382378	GACCATTGTGAGGAC[A/T]ATGTTAATTTAAAAT	57674
rs74003703	snp	A/G	0.0475351	0.146656	intron-variant	RNF213	GRCh38.p7	17:80274103	CCTGAGCGTCCGCTG[A/G]GTGCGTGTCTTGCGC	57674
rs74003706	snp	C/G	0.0112027	0.0739991	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288162	CCACACGGAAGGGGA[C/G]GACCAGGACGCTTCC	57674
rs74003721	snp	A/C	0.0391387	0.134304	intron-variant	RNF213	GRCh38.p7	17:80298053	GACCCTGCGTTGACT[A/C]CTTAGCCAGGACCCC	57674
rs74003748	snp	C/G/T	0.416545	0.186448	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355581	AAGAAGCGGGGTGAG[C/G/T]GGGAATGGGGGCTTA	57674
rs74256841	snp	C/T	0.122758	0.215196	intron-variant	RNF213	GRCh38.p7	17:80276572	AAAAGAGGCCAGGCG[C/T]GGTGGCTCACTGGGT	57674
rs74256843	snp	C/T	0.0766824	0.180169	intron-variant	RNF213	GRCh38.p7	17:80281710	CATCTCATACTCACA[C/T]TGAAACACACAGTGG	57674
rs74347091	snp	A/G	0.18325	0.240924	intron-variant	RNF213	GRCh38.p7	17:80273910	CAGGTGTGAGCCACC[A/G]CGCCCGGCCTCCACC	57674
rs74367834	snp	A/T			splice-donor-variant	RNF213	GRCh38.p7	17:80273406	GGACCGTCCAAGAAG[A/T]GAGTGCACTGCCTCG	57674
rs74380207	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80329248	TCCTGAGAAAAGGGC[A/G]TGTAAGAGGTTAAAC	57674
rs74380888	snp	C/T	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80318041	TGTCTGGCTGGCTCT[C/T]CCCTGAAGTCAGGAC	57674
rs74426311	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB	RNF213	GRCh38.p7	17:80258856	GGCCCAGCACTATTA[C/T]GTGGGCAAGAGGCAA	57674
rs74455936	snp	A/C/T	0.00740718	0.0604054	missense	RNF213	GRCh38.p7	17:80306464	AGCAAGTCTTGAATA[A/C/T]GCAGGTTTGTGTCTG	57674
rs74458279	snp	C/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80348341	CCAAGAGTCCTAAAT[C/G]CCTCGTGTCAGGATT	57674
rs74467669	snp	G/T	0.0205511	0.0992634	intron-variant	RNF213	GRCh38.p7	17:80272932	TTAGAGGTGCCCGAG[G/T]TGCGCTGACATCCTA	57674
rs74490096	snp	A/G	0.00256659	0.035731	missense	RNF213	GRCh38.p7	17:80290637	CTTCATTTCCCATTC[A/G]ATCCTGACCTCCATA	57674
rs74506458	snp	A/G	0.0115144	0.0749975	intron-variant	RNF213	GRCh38.p7	17:80268493	GCCTTTGTGGAAGAC[A/G]GGTGGATCTTGGGAA	57674
rs74522255	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355468	GAGGAAGAGGGGTGA[A/C]CGGGAATGGGGGCTC	57674
rs74524090	snp	A/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80337455	TGGGTGGGCGACTGC[A/G]TCCTGAGCCCTGGGG	57674
rs74533354	snp	C/T	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270501	CCTTCTAGATTTCTA[C/T]TCAGATTCTCTCCAG	57674
rs74560936	snp	A/T	0.0225045	0.103662	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395523	TCCTGGCGACTCCAC[A/T]GTGGAGCTGAGCGCC	57674
rs74592392	snp	C/T	0.0879971	0.190408	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389554	CAGTAGAGACAGACA[C/T]GCGCTAGAAATGCCA	57674
rs74651365	snp	A/G	0.00080691	0.02007	synonymous-codon	RNF213	GRCh38.p7	17:80344932	GGAGGAATGCCTCCA[A/G]CATTTCCTGTTTCAC	57674
rs74652294	snp	A/C	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396746	CCCACCCCCCCCCCC[A/C]AACCAGAGCAACTTT	57674
rs74687017	snp	C/T	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270243	GCCACCCAGCAGGGC[C/T]TGACTCAGCAACAGG	57674
rs74692190	in-del	-/ATGGTGATGGTTGGTGGTGGTG			intron-variant	RNF213	GRCh38.p7	17:80313481	ATGGTGGTGGAGGTG[-/ATGGTGATGGTTGGTGGTGGTG]GTGGTAGAGGTGATG	57674
rs74703406	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355535	TACAGGGGGAAGAAG[C/T]GGGGTGGACGGGAAT	57674
rs74712613	snp	C/T	0.000131811	0.00811715	intron-variant	RNF213	GRCh38.p7	17:80308988	CTCCTAAATCCTTGC[C/T]GGGATTTCTCTTAAC	57674
rs74715712	snp	C/T	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395095	TCTTTCTGTGAAGGC[C/T]TTTTTTTTCCTTTGG	57674
rs74769342	snp	A/C	0.196022	0.25834	intron-variant	RNF213	GRCh38.p7	17:80269657	ATCTATTCATCCATC[A/C]ATCTATCCATCCATC	57674
rs74789968	snp	C/T	0.0908922	0.192833	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371790	CACACACAGGACAGA[C/T]GACCGATAGATAGAT	57674
rs74790219	snp	A/G	0.231482	0.249313	intron-variant	RNF213	GRCh38.p7	17:80318979	AGGTGCTTTTTCTGC[A/G]GAGTGGGAAAAGAGA	57674
rs74792814	snp	C/G	0.000609319	0.0174439	missense	RNF213	GRCh38.p7	17:80345189	CCATGGATGGGGTTA[C/G]GGAAGAAGATCTAGC	57674
rs74816311	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80293073	TATATATATTTTTTT[C/T]CTGAGACAGGATCTC	57674
rs74843574	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80272283	AGCAAGACTCTGTCT[A/C]AAAAAAAATAATAAA	57674
rs74870219	snp	C/G	0.188316	0.242271	intron-variant	RNF213	GRCh38.p7	17:80280681	GCTGGTCTCAAACTC[C/G]TGGGCTCAAGCAATT	57674
rs74900260	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283167	CTATGAAACTGTTCA[A/G]TGGAAAAGCAGACAG	57674
rs74946385	snp	C/T	0.0103295	0.0711199	intron-variant	RNF213	GRCh38.p7	17:80306089	CCCGAGTCAGCCTCC[C/T]AAGTATTGGGATTCA	57674
rs74948790	snp	G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368449	TTTTTTTTTTTTTTT[G/T]TGAGACAGTGTTTCA	57674
rs74980179	snp	C/T	0.0217236	0.101931	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366570	TCCTTTGCCCATTTT[C/T]GAATTGGGTTGTTGA	57674
rs74984522	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366057	TTAGTTTTCCTGCTG[A/G]AAGCCTGACTTGTAC	57674
rs74996847	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80308337	AGTCCTTTCTTACAC[C/T]GCCTTCCCAGTCCCC	57674
rs75053281	snp	A/C/G	0.0106769	0.0723032	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385207	GACCAGGACTGTCCC[A/C/G]CATTTGGCGGTTCGA	57674
rs75101672	snp	C/T	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270426	TACAATGCAAATCTC[C/T]TCAAATCCCCTGCAC	57674
rs75103555	snp	C/T	0.375	0.216506	intron-variant	RNF213	GRCh38.p7	17:80299887	AAAAGAATGAGTTCA[C/T]GTCCTTCACAGGGAC	57674
rs75142558	snp	C/G	0.0984431	0.198823	intron-variant	RNF213	GRCh38.p7	17:80274517	TGGCTTTCTGTCTGT[C/G]GTTCCTTGTAGGTGG	57674
rs75145348	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382199	ATGTTAAAAAAAAAA[A/G]GCTATAAAATATTGT	57674
rs75149246	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80275821	GCACCCGCCACCACG[C/T]CTGGCTAATTTTTTG	57674
rs75154501	snp	A/G	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80271353	GCTACGCCAACACTG[A/G]GTACTCAAAGGGAAA	57674
rs75161557	snp	C/G/T	0.00144893	0.0268772	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379678	CGCCGATTGGAGGCA[C/G/T]TGACCACAAACCTCG	57674
rs75223398	snp	G/T	0.0360663	0.129354	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287402	CAGCTACTCAAGAGG[G/T]TGATGGGGGAGGATC	57674
rs75304542	snp	C/T	0.00559133	0.0525776	intron-variant	RNF213	GRCh38.p7	17:80328008	AGCATCGAGTCGATA[C/T]GCACTTCAGGCTCCT	57674
rs75340782	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80271159	CTCAGAATCCCTGGT[-/T]GTAGGTGAAACAGCA	57674
rs75354271	snp	A/G	0.039522	0.134904	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394194	TTGGTTTTCTCACGC[A/G]TAAAATGGAGAGTGG	57674
rs75394830	snp	A/G	0.0391387	0.134304	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365725	TAGTAGGACACAGCC[A/G]GTGCCCCCCTTCCAC	57674
rs75498886	snp	A/C	0.0603597	0.1629	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359012	CTAGCCAGACCCAGC[A/C]TGGCGTGACACGGAG	57674
rs75537759	snp	A/G	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270711	CTTTGGTTGGTCCTT[A/G]TGATTGTTGGGACTG	57674
rs75541508	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80334629	AGGTTTTTTTTTTTT[G/T]TTTGTTTGTTTTTTT	57674
rs75587883	snp	C/G	0.0271762	0.113356	intron-variant	RNF213	GRCh38.p7	17:80279118	GAGGATGTTTTGCTA[C/G]TGGTGAATTTCAGCT	57674
rs75595842	snp	A/G	0.0883596	0.190715	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388431	CTCCGCTGGATTCCC[A/G]GTTGTGTTACTATTT	57674
rs75626741	snp	C/T	0.190205	0.242744	intron-variant	RNF213	GRCh38.p7	17:80285014	CTCAAACCATGCAGC[C/T]GATAACAGGGAGAGC	57674
rs75650429	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355469	AGGAAGAGGGGTGAC[C/T]GGGAATGGGGGCTCA	57674
rs75651507	snp	A/G	0.00433442	0.0463511	synonymous-codon	RNF213	GRCh38.p7	17:80337847	GATTTCCCCAGACAC[A/G]GTTCTGCACTTGATC	57674
rs75667133	snp	C/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80277202	GATATGAAATATCCA[C/T]GATAGACTCACCCAT	57674
rs75694445	snp	G/T	0.0228947	0.104514	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377181	CATTTCTTTGTCGTG[G/T]GGAAAAGGCCCTCTG	57674
rs75698793	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80333242	TTTTTTTTTTTTTTT[A/T]GCAGAGACAGGGTTT	57674
rs75705387	snp	C/T	0.00118855	0.0243488	synonymous-codon	RNF213	GRCh38.p7	17:80298483	CGCTCTGGAGGGACT[C/T]TCCTTCTCACCGTTC	57674
rs75709900	snp	C/T	0.0252325	0.109451	intron-variant	RNF213	GRCh38.p7	17:80317465	AGCGCTTCGGAGTCT[C/T]ACTGAGAGGACAGAG	57674
rs75757378	snp	A/G	0.0475351	0.146656	intron-variant	RNF213	GRCh38.p7	17:80272290	CTCTGTCTCAAAAAA[A/G]ATAATAAAATAAAAT	57674
rs75771827	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80268636	ATCCATCCATCCATC[C/T]GTTTATCTGTCTATC	57674
rs75818622	snp	C/T	0.00438388	0.0466124	intron-variant	RNF213	GRCh38.p7	17:80344037	ACTGTGGGGCGTTTT[C/T]GCCTGGCGTGGGGGG	57674
rs75842986	snp	C/G	0.181659	0.240478	intron-variant	RNF213	GRCh38.p7	17:80275534	GCCACACAAATGCTC[C/G]AGCAGGACGCACTCG	57674
rs75849277	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368278	AACTATCATAAGAGA[C/T]GCCACTTACGTACTT	57674
rs75869454	snp	C/T	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357991	AGACCCTCACATACA[C/T]GTTTTAAAAATAAAA	57674
rs75876853	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80298831	AAAAAAAAAAAAAAT[A/T]AGCCAGGTGTGGTGG	57674
rs75886879	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366113	AGCCCTTGGGACCAT[C/T]TGAAACAAGAGGCTT	57674
rs75921209	snp	C/T	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270972	CTGAGTGGCAGAAAC[C/T]CCAGTAAGGGTCCAG	57674
rs76011856	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80266279	GAGCCCCATCTCTAC[A/C]AAAAAAAAAAAGAAA	57674
rs76019210	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366428	ACTATCTGATTTTTT[C/T]CATAATGGCCACCGT	57674
rs76095531	snp	C/G	0.0799831	0.183287	intron-variant	RNF213	GRCh38.p7	17:80262943	CAGAAGAAGGTGGTG[C/G]GTGGGCCAGTGTGCC	57674
rs76121974	snp	G/T	0.0154538	0.0865337	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364027	CTGTGTACTGGGGCC[G/T]TAGAAAGGCAGACGG	57674
rs76164172	snp	C/G	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270469	GCCACTCACTGGCCG[C/G]GTCTCTGTGCTCCCT	57674
rs76220116	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368579	CTGGGATTACAGGCA[C/T]GCACCACCATGCCCG	57674
rs76221186	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80333228	TAATTTTTTTGGTAT[A/T]TTTTTTTTTTTTTAG	57674
rs76225497	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274592	CTGTGGTCTGTGGGG[A/G]GTGAGTGGGGTGAGT	57674
rs76254032	snp	C/T	0.00572994	0.0532178	intron-variant	RNF213	GRCh38.p7	17:80291860	GCTGTCTGCTCACCC[C/T]TCCGGAGTGCAGGTG	57674
rs76269241	snp	C/T	0.0484096	0.147856	intron-variant	RNF213	GRCh38.p7	17:80273431	GCCTCGGCTCCCCTC[C/T]GCCCCCGCTCACTCT	57674
rs76285796	snp	A/G	0.129664	0.219133	intron-variant	RNF213	GRCh38.p7	17:80262497	CTCAGAGGAACTGGC[A/G]AGGCCGCAGGCACTC	57674
rs76287106	snp	A/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80269185	GCTGCCCACCCACAT[A/G]GAGGGTGGGTCTTCC	57674
rs76299780	snp	A/C	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270738	ACTGTTTATACTGGG[A/C]ACAGCCTGAAACCCA	57674
rs76300944	snp	A/G	0.0337553	0.125452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391254	TTATCACCCATTTGT[A/G]TATCATCCTCTGAAT	57674
rs76351115	snp	A/G	0.00716266	0.059414	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353230	ATCATAGAGCACCAG[A/G]GCCGAGCAGGTGCGC	57674
rs76356550	snp	C/T	0.00575987	0.053355	intron-variant	RNF213	GRCh38.p7	17:80331997	GACACTTTCTTTTCG[C/T]TTCTAAAGTGGACTT	57674
rs76370064	snp	C/T	0.00136712	0.0261092	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373150	GGTGTTTCCCAAGGA[C/T]GTTGTCAAGCAGCAG	57674
rs76374987	snp	A/G	0.00421617	0.0457199	synonymous-codon	RNF213	GRCh38.p7	17:80273269	TAACTCCACAATGGC[A/G]TCGGCCTCGGAGGGT	57674
rs76420316	snp	A/C/T	1.6504e-05	0.00287258	missense, synonymous-codon	RNF213	GRCh38.p7	17:80345505	GGCCACCGACCCCGA[A/C/T]AAAACGTATGAGCTC	57674
rs76434378	snp	A/G	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80280325	TCCGTGGAGAGGTGG[A/G]CCCTTCCCCAGAGAG	57674
rs76450493	snp	A/G	0.039522	0.134904	intron-variant	RNF213	GRCh38.p7	17:80302455	GTATATACAGTGCAT[A/G]AAATGTATTCTCTGT	57674
rs76451336	snp	A/G	0.0345262	0.126772	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369213	AAACCAGCCTGGCCA[A/G]CACGGTGAAACCCCA	57674
rs76458306	in-del	-/ATCT			intron-variant	RNF213	GRCh38.p7	17:80268656	TCTGTCTATCTATCT[-/ATCT]GTCATCTGTCTTCTA	57674
rs76462508	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80301905	CCCGCAGATGAGTGG[A/C]TGAAGAAAGTGTTGT	57674
rs76495321	snp	C/T	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80264917	GCAGGGCCTTTGCAC[C/T]ACCCTTCCCCAGAGG	57674
rs76524822	snp	C/T	0.0944967	0.195752	intron-variant	RNF213	GRCh38.p7	17:80261489	CCGGCGGGCCGGGCC[C/T]TGGGGGAGTCCAGGG	57674
rs76588943	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368622	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	57674
rs76603065	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368631	AGAGACAGGGTTTCA[C/T]CATGTTGGCCAGGCT	57674
rs76619301	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356471	GTGGTGGCCAGACCC[A/G]CACCCTCAGCTCACC	57674
rs76697902	snp	G/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80285689	CTTTTTTTTTTTTGT[G/T]AGATGGAGTCTTGCT	57674
rs76755347	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368533	CACCTCCTGGGTTCA[A/G]GCAATTCTCCTGCCT	57674
rs76805790	snp	A/T	0.00597247	0.0543191	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80386107	GCATTTGAAACTCTA[A/T]CAGCATATGAGATGG	57674
rs76839993	snp	A/C/G	9.88484e-05	0.00702954	missense, synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288713	GACCCAGAGAATGAA[A/C/G]CAGCCACCAGCAACC	57674
rs76868615	snp	A/C	0.277778	0.248452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355505	GAAGAAGCGGGGTGA[A/C]CGGGAATGGGGGCTT	57674
rs76886219	snp	A/G	0.0588605	0.161139	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382555	ATTTCAGCAAAGTGA[A/G]CACACCCAGAGTCAC	57674
rs76908024	snp	C/T	0.0217236	0.101931	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360621	CAGAAGGCACGAGCG[C/T]CTGGAGCATCCCCTA	57674
rs76918558	snp	A/G	0.000337217	0.0129806	missense	RNF213	GRCh38.p7	17:80347169	AAACGGTGTGTAAGC[A/G]CCAGGACAAGGAATT	57674
rs76918788	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80318279	GAGAGAGTAGGCACA[C/T]GGGGATAGAGGTTCT	57674
rs76934686	snp	A/G/T	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80308957	CTAGTCATCAATGGT[A/G/T]ACCATTTTCTGGCTT	57674
rs76971781	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355544	AAGAAGCGGGGTGGA[C/T]GGGAATGGGGGCTTA	57674
rs76985739	snp	G/T	0.00285339	0.0376637	synonymous-codon	RNF213	GRCh38.p7	17:80334107	CTTTTTCTTGCAGAC[G/T]GATAACTTCGACGAC	57674
rs76987882	snp	C/G	0.000844119	0.0205267	intron-variant	RNF213	GRCh38.p7	17:80328303	TGCTGTATTGGGTTA[C/G]TTTATTGGTGTTCTT	57674
rs77010918	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355558	ACGGGAATGGGGGCT[C/T]ATGGAGGAAGAAGCG	57674
rs77019370	snp	A/C	0.00716266	0.059414	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367621	ACAGGATCACAAAGG[A/C]CTCGCACCCCACACC	57674
rs77072070	snp	A/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268241	TGTGAATCGTGCTAC[A/G]GTGAGCATGGGTGTG	57674
rs77073491	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368517	AGCTCACTGCAACCT[C/T]CACCTCCTGGGTTCA	57674
rs77175089	snp	A/G	0.0614824	0.164198	intron-variant	RNF213	GRCh38.p7	17:80295262	GAGAGTGGAAGGAAC[A/G]GGGCACCCTCTGTCA	57674
rs77239314	snp	G/T	0.00429066	0.0461186	missense	RNF213	GRCh38.p7	17:80291763	CATTTACAAGCACCA[G/T]CAGAAGAAGGGCGAG	57674
rs77272340	snp	A/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80308500	TAAGTCCCCTCCTGA[A/G]TCCCTCCTAAGGCTC	57674
rs77343982	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387969	TTTTTTTTTTTTTTT[C/T]TTTTTTTTGAGACGG	57674
rs77346175	snp	A/G	0	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397661	CCCTTAAAAGGGACA[A/G]GAATTGCTCACTCGG	57674
rs77357854	snp	C/G	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80311411	GCTGTCCAGCCCTGT[C/G]CTGCTGGATTGTTCT	57674
rs77374257	snp	A/G	0.0158469	0.0875917	intron-variant	RNF213	GRCh38.p7	17:80333902	TTCCCAGGAATCACA[A/G]TTCATCTTGATCAGG	57674
rs77398988	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387408	ACTGCACCCAGCTGA[C/T]TGTTGAGGTCTTGAT	57674
rs77421497	snp	C/T	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80270845	TACTAGGGCTTTGCT[C/T]CATTTCTCTGATCCT	57674
rs77432320	snp	G/T	0.0501905	0.150254	intron-variant	RNF213	GRCh38.p7	17:80275357	GTGGGAAAGTGGCAG[G/T]ACGGATGGTGTTCCT	57674
rs77437144	snp	C/T	0.00636936	0.0560724	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361052	TGAAGAGCAGCCCAC[C/T]TGTTCCTAATTTACT	57674
rs77473882	snp	C/T	0	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393869	GCACTGCCCACCCCT[C/T]TTTTTTTTTTTCTTC	57674
rs77490736	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80266291	TACAAAAAAAAAAAA[A/G]AAAAAAAAATACAAG	57674
rs77506504	snp	A/G	0.0361502	0.129492	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367976	GTTTGGGATTCAGCC[A/G]TGCTCCATCTGCCTG	57674
rs77528989	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80273615	GGGCCTCCACCGTCT[C/T]TTTTTTTTTTTTTTT	57674
rs77574627	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367124	TGGACCTAAGGTATC[A/G]TGAAGAGAATGAGTT	57674
rs77615602	snp	A/G	0.0193772	0.0965046	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371795	ACAGGACAGACGACC[A/G]ATAGATAGATGCTCT	57674
rs77628562	snp	C/G	0.0279526	0.114869	intron-variant	RNF213	GRCh38.p7	17:80309558	GGACCATTTTCCTCC[C/G]AAAAAATACATGTCC	57674
rs77638913	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80271158	GGCTCAGAATCCCTG[A/G]TTGTAGGTGAAACAG	57674
rs77699519	snp	C/G	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392954	AAAAAGTAACATGAG[C/G]GGACTGATTGGTCCC	57674
rs77707505	snp	A/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366680	AAATAAAAAAAAAAA[A/T]ATCTGTAAATGTCAT	57674
rs77869167	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355654	GAAGAAGCGGGGTGG[A/C]CGGGAATGGGGGCTT	57674
rs77881326	snp	G/T	0.077417	0.180873	intron-variant	RNF213	GRCh38.p7	17:80272369	ACTGAGAAGTTCAGG[G/T]CCTGGCCCTGATGTC	57674
rs77927923	snp	A/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268890	AGCTGGGAAAGAAAG[A/G]AGCCAGTAGTTGCTC	57674
rs77956633	snp	A/C	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80272870	CCACCCTGGGGAAGA[A/C]AGGAGGAATGTCTAC	57674
rs77993707	snp	A/G	0.123452	0.215605	intron-variant	RNF213	GRCh38.p7	17:80268446	ACTCCAAAGATGCAG[A/G]GGTGGGGATTCCCAT	57674
rs77997074	snp	A/T	0.0271762	0.113356	intron-variant	RNF213	GRCh38.p7	17:80302975	TTCTAAGCAAAATAG[A/T]TTAATTTATTTTGGC	57674
rs78032871	snp	C/T	0.0337553	0.125452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389443	CGAGGGATAGGAGCA[C/T]TCAGGGAGTGCCACT	57674
rs78063795	snp	A/G	0.198324	0.244601	intron-variant	RNF213	GRCh38.p7	17:80281142	ACACCCCCACACCCC[A/G]CTCACACCACTCACA	57674
rs78095180	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269384	CCCTATCTATCTATC[C/T]ACCTATCCATCTGTC	57674
rs78119017	snp	A/T	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80317394	GGCAGGGATGGGGTG[A/T]ATCACAGCTCCGTGT	57674
rs78134045	snp	A/G	0.0271762	0.113356	intron-variant	RNF213	GRCh38.p7	17:80280863	AGTAAAGCTGTCAAC[A/G]TACACGGGTGGAAAC	57674
rs78158446	snp	C/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80269144	TCTGCCTGCTTTGTT[C/T]TAGCCACGCTGGCAG	57674
rs78184798	snp	G/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80285688	GCTTTTTTTTTTTTG[G/T]GAGATGGAGTCTTGC	57674
rs78230659	snp	A/G	0.441841	0.160303	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355617	GAAGAAGCGGGGTGA[A/G]TGGGAATGGGGGCTT	57674
rs78234279	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366115	CCCTTGGGACCATTT[G/T]AAACAAGAGGCTTGG	57674
rs78297219	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80298829	AAAAAAAAAAAAAAA[A/T]TTAGCCAGGTGTGGT	57674
rs78311209	snp	G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368492	GGCTGGAGTACAGTG[G/T]CACGATCTCAGCTCA	57674
rs78323445	snp	C/T	0.187053	0.241946	intron-variant	RNF213	GRCh38.p7	17:80303236	CTCCTTCCCCTAGCC[C/T]GGAGGCTCAGGCCAC	57674
rs78346200	snp	A/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366669	AGGATGGCTCAAAAT[A/T]AAAAAAAAAAAATCT	57674
rs78410347	snp	A/G	3.63412e-05	0.00426254	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389400	AAGGAAATCAGCACA[A/G]CCCCTCACCCTGGTC	57674
rs78418072	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290180	TCTTCCTCCATTTTG[C/G]AGGCAGTGAAGAGAG	57674
rs78428708	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80268635	CATCCATCCATCCAT[C/T]CGTTTATCTGTCTAT	57674
rs78432554	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80293074	ATATATATTTTTTTT[C/T]TGAGACAGGATCTCG	57674
rs78457838	snp	C/T	0.00615237	0.0551211	missense	RNF213	GRCh38.p7	17:80343174	ACGACAAAATGAAGA[C/T]GCAGTTAAACGTGAA	57674
rs78502418	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381260	AGGCTGACATCTTCA[C/T]TATTTTACCTGTGTC	57674
rs78513297	snp	C/G	0.131381	0.220067	intron-variant	RNF213	GRCh38.p7	17:80269846	TCTCTGGATAACCCT[C/G]TTCTATACTGTGAGT	57674
rs78540366	snp	C/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268973	TCTGTGGCTGAAGAC[C/T]CGAGATCCCCCTGGC	57674
rs78554433	snp	A/G	0.182296	0.240658	intron-variant	RNF213	GRCh38.p7	17:80275787	CCTACTTCAGCCTCC[A/G]GAGTAGCTGGGACTA	57674
rs78567340	snp	A/G/T	0.117886	0.21224	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398861	TTTAAAAGCCAAGAT[A/G/T]AATTTAAAACCTATA	57674
rs78602072	snp	A/C	0.0626037	0.165477	intron-variant	RNF213	GRCh38.p7	17:80328587	GAGAGAAGGCTTTAA[A/C]ATTTTTTTTTTAATT	57674
rs78614412	snp	C/T	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368802	AACCCACTTCTTGTC[C/T]AGCTTTTTGGAGCTG	57674
rs78639507	snp	C/T	0.0916144	0.193427	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378726	CATGAAATGAGGACG[C/T]TGAAATAGAGTCTAT	57674
rs78676934	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326229	TCCCGGGCTCACGTG[A/G/T]TCCTCCTGCCTCAGC	57674
rs78689692	snp	A/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368458	TTTTTTTTGAGACAG[A/T]GTTTCACTCTGTTGC	57674
rs78693036	snp	A/T	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80272306	ATAATAAAATAAAAT[A/T]AAAAAAGAAAAAGAA	57674
rs78697648	snp	A/G	0.0193772	0.0965046	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376104	ACAGAATAGAATATC[A/G]AAATTAATGCTTACG	57674
rs78725532	snp	A/G	0.122064	0.214785	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353741	TTTAAACGCTTTTGC[A/G]TTGGGAGCTAGAGGA	57674
rs78733284	snp	C/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268396	GCAGTACTGCATCCC[C/T]GGAGGGACTGCAGGG	57674
rs78740161	snp	C/T	0.00636936	0.0560724	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353762	AGCTAGAGGAGTCGC[C/T]GCCGCTGTGCAGGGG	57674
rs78754188	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366116	CCTTGGGACCATTTG[A/C]AACAAGAGGCTTGGG	57674
rs78757882	snp	G/T	0.0333695	0.124785	intron-variant	RNF213	GRCh38.p7	17:80283296	CGGGAAGAGCTGAGG[G/T]GGTGAGCCTGGGGCT	57674
rs78790530	snp	C/T	0.039522	0.134904	intron-variant	RNF213	GRCh38.p7	17:80331086	AGCCTCCCAAAGTGC[C/T]GGGATTACGGGCGTG	57674
rs78795452	snp	C/T	0.000803443	0.0200269	intron-variant	RNF213	GRCh38.p7	17:80337732	TGGCCAAAAGGTGAG[C/T]GGTCCCCAGCCCTCG	57674
rs78796464	snp	C/G	0.00517822	0.0506191	intron-variant, missense	RNF213	GRCh38.p7	17:80288898	CCTTCGGGGTGCTCA[C/G]ATTCCAGCGGAGAGA	57674
rs78857404	snp	C/G	0.145863	0.227279	intron-variant	RNF213	GRCh38.p7	17:80313186	GGCATTTGGCCGAAG[C/G]CTTCTGGGTAGGGAT	57674
rs78862091	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274612	GTGGGGTGAGTGTGG[A/G]GGGTGAGTGGGGTGT	57674
rs78865500	snp	C/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390456	AGTAATCTCAACTCA[C/G]TGCAACCTTGGCTCA	57674
rs78865912	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368582	GGATTACAGGCATGC[A/G]CCACCATGCCCGGCT	57674
rs78885550	snp	C/T	0.0111196	0.0737302	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371394	GCAGGGCAGGCAGGC[C/T]GCTGACTTCCAGGAG	57674
rs78890172	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328822	GCTTCCTGTTTTCTC[A/C/G]TAACGGAGTTGCATC	57674
rs78912458	snp	C/T	0.00867673	0.0652923	synonymous-codon	RNF213	GRCh38.p7	17:80344707	CCAGTTCAGTTTTCT[C/T]GACATCTTCCCAAAA	57674
rs78921126	snp	A/G	0.200182	0.244986	intron-variant	RNF213	GRCh38.p7	17:80285110	GTGTGGACAGTGACC[A/G]TGACCACAGCATCAC	57674
rs78930901	snp	A/C	0.0479149	0.147179	intron-variant	RNF213	GRCh38.p7	17:80267594	CCACAGTAAAGCCCT[A/C]ACTCTCCTGTAGCCA	57674
rs78972362	snp	G/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80334624	CAGAGAGGTTTTTTT[G/T]TTTTGTTTGTTTGTT	57674
rs78979716	snp	C/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354669	CATCCGGGCCATGGG[C/G]ACTGAGCTGTTTCTT	57674
rs79000983	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355504	GGAAGAAGCGGGGTG[A/G]CCGGGAATGGGGGCT	57674
rs79016046	snp	A/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374005	GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAA	57674
rs79024264	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80334937	GGCCTTTTTTTTTTT[-/TT]GAGACGGAGTTTCGC	57674
rs79073011	snp	G/T	0.105214	0.203807	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378776	TGAAATTCTGTAACT[G/T]GTTTGGTGTGTTATC	57674
rs79078595	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80310557	TGCACCCAGCACAAT[A/T]TTTTTTTTTTTTGAG	57674
rs79078690	snp	A/G	0.0799831	0.183287	intron-variant	RNF213	GRCh38.p7	17:80263293	GTGAGGCATCAGCAG[A/G]CTGAGCGCCTTGCTC	57674
rs79083522	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396266	GACCCTGTCTCAAAA[A/T]AAAATAAAATAAGGA	57674
rs79137949	snp	C/G	0.0475351	0.146656	intron-variant	RNF213	GRCh38.p7	17:80274529	TGTCGTTCCTTGTAG[C/G]TGGCACTCCATGGTT	57674
rs79141647	snp	C/T	0.0325976	0.123435	intron-variant	RNF213	GRCh38.p7	17:80308743	ATAAACATCCCTTGC[C/T]TTTTTTCACATCTTG	57674
rs79146856	snp	C/T	0.0283406	0.115616	intron-variant	RNF213	GRCh38.p7	17:80291953	CCTCTTTGCTCTGCA[C/T]TGACCCCGCCCCAGC	57674
rs79147399	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355543	GAAGAAGCGGGGTGG[A/C]CGGGAATGGGGGCTT	57674
rs79170599	snp	C/G	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396744	CCCCCACCCCCCCCC[C/G]CCAACCAGAGCAACT	57674
rs79200287	snp	A/T	0.0611083	0.163768	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396694	ACGAATCCCGTTTCC[A/T]GCTGGAAAAACAAGC	57674
rs79206840	snp	C/T	0.0988009	0.199095	intron-variant	RNF213	GRCh38.p7	17:80273911	AGGTGTGAGCCACCG[C/T]GCCCGGCCTCCACCT	57674
rs79226410	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390865	GCCAGAAGTTTAAGA[A/C]CAGCCTGGCCAACGT	57674
rs79267010	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321395	GGCCAAATATTCCCC[A/G]TTTATCCATGTGTCC	57674
rs79268626	snp	A/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80334324	AAGTTTTCAGATGGC[A/G]CACTGTGTGGCGTTC	57674
rs79283319	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382200	TGTTAAAAAAAAAAA[A/G]CTATAAAATATTGTA	57674
rs79300455	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380502	TCCCAAACTCTAGCT[A/G]TTCTTAGCCCAACCG	57674
rs79304820	snp	C/T	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80272334	GAAAAAAGAGGTTTA[C/T]TTAGCTCACAGTTCT	57674
rs79309797	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80322873	TTTTGAAGCACAGAA[A/G]TCTTTAATTTTGAAG	57674
rs79367959	snp	A/C	0.157311	0.232183	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384569	GGAGTATGAGTTCAC[A/C]ATGACAGGAAGGACT	57674
rs79376586	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355632	GTGGGAATGGGGGCT[C/T]ACAGGGGAAGAAGCG	57674
rs79409057	in-del	-/TCCG	0.0792508	0.182605	intron-variant	RNF213	GRCh38.p7	17:80269761	CATCTTATCTATCCA[-/TCCG]TCCATCCATCCATGT	57674
rs79434821	snp	A/C	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396734	GTGCATTTCCCCCCC[A/C]CCCCCCCCCCCCAAC	57674
rs79437938	in-del	-/C	0.199254	0.244796	intron-variant	RNF213	GRCh38.p7	17:80280111	TGGGCTGGGGCTTGG[-/C]CCGTGAGCCCACTCC	57674
rs79445943	snp	A/G	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375435	CAGCGGTGCGGGGGC[A/G]TCTATCCTATAATCC	57674
rs79514603	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385739	TGTGTTTGTTTGTTT[C/T]TGAGATGGAGTCTTG	57674
rs79518180	snp	A/G	0	0	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260516	CGCCTGCGCGGGGCC[A/G]GCGGCGGCGGCGGGC	57674
rs79544074	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366534	CATTTGCTGTCTTCT[C/T]TGGAGAAATGTCCAT	57674
rs79554822	snp	A/T	0.0333695	0.124785	intron-variant	RNF213	GRCh38.p7	17:80280418	CCAACTAATTAATGT[A/T]TAACAGTAGTATAGC	57674
rs79587330	snp	A/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80349668	TGTGGCAACTGCACC[A/G]CGCTGAACATCGCAG	57674
rs79589259	snp	A/G	0.0603597	0.1629	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366130	GAAACAAGAGGCTTG[A/G]GGGAAAGCCCTGCCT	57674
rs79604144	snp	C/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373279	CACCCCACCCCCTCA[C/G]ACCTTCCCCACCACA	57674
rs79606551	snp	C/T	0.0325976	0.123435	intron-variant	RNF213	GRCh38.p7	17:80308756	GCCTTTTTTCACATC[C/T]TGGAACGCACTGAGG	57674
rs79624919	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80273613	TGGGGCCTCCACCGT[C/T]TTTTTTTTTTTTTTT	57674
rs79657648	snp	G/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268865	GAAGTCCCATGGTAG[G/T]CCGTCTGCAAGCTGG	57674
rs79695842	snp	C/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80268096	AAAGTACCGGGGCTA[C/T]AGGCATGAACCATTG	57674
rs79730629	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80301971	AAGAATGAAATTCTG[C/T]CATTTGTGACAATAT	57674
rs79787507	snp	C/T	0.000899715	0.0211908	synonymous-codon	RNF213	GRCh38.p7	17:80346537	GGATCTTTTTCTGGA[C/T]GGCGTACCTCTGAGG	57674
rs79792282	snp	C/G	0.00682933	0.0580347	missense	RNF213	GRCh38.p7	17:80306265	AGGAGTTCCCTACTT[C/G]AGTTTATGAGAGAGA	57674
rs79819283	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80267826	CAGATTTTCTTTTCT[C/T]TTTTTTTTTTTGAGA	57674
rs79859284	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80312164	AAGAAAAGAAAAAGA[A/C]CACACATTAATCCAG	57674
rs79876928	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80269764	CTTATCTATCCATCC[A/G]TCCATCCATCCATGT	57674
rs79899846	snp	C/T	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355506	AAGAAGCGGGGTGAC[C/T]GGGAATGGGGGCTTA	57674
rs79916079	snp	A/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80309434	GTGTGGCCATCAGCT[A/G]GTCATGGGGAAACCA	57674
rs79975611	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368580	TGGGATTACAGGCAT[A/G]CACCACCATGCCCGG	57674
rs80006523	snp	A/C/T	0.039522	0.134904	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394449	AAACCAGTTATGTTT[A/C/T]GGAAAGAGGGAAAAG	57674
rs80014477	snp	A/C/G	0.0103295	0.0711199	intron-variant	RNF213	GRCh38.p7	17:80291470	TCAAGAAGTCCTCCC[A/C/G]CCTCAGCCTCCCATG	57674
rs80034830	snp	A/G	0.00755907	0.0610114	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354920	TGAAGTTAAAATGAC[A/G]TGCAGAGCAGGCAGG	57674
rs80057807	snp	C/T	0.0991586	0.199366	intron-variant	RNF213	GRCh38.p7	17:80271200	GGATGGGGCCTTGGG[C/T]CGCCTGTTGCAGATC	57674
rs80088970	snp	A/G	0.0298908	0.118541	intron-variant	RNF213	GRCh38.p7	17:80324526	ATAAATTAACCTTGT[A/G]GTTTTTACTAATTAC	57674
rs80097023	snp	A/G	0.00187694	0.0305769	missense	RNF213	GRCh38.p7	17:80343296	TATCAGAAGGTCCCC[A/G]TGCTCTTTCACCTGG	57674
rs80129171	snp	A/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368493	GCTGGAGTACAGTGG[A/C]ACGATCTCAGCTCAC	57674
rs80129570	snp	C/T	0.197082	0.244335	intron-variant	RNF213	GRCh38.p7	17:80285300	GTTGCCCAGCCATTG[C/T]AGCATGGGGTGAGCT	57674
rs80131819	snp	C/T	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355618	AAGAAGCGGGGTGAG[C/T]GGGAATGGGGGCTTA	57674
rs80188698	snp	C/T	0.0325976	0.123435	intron-variant	RNF213	GRCh38.p7	17:80308519	CTCCTAAGGCTCCTC[C/T]CGAGTCCCTACCGAG	57674
rs80255367	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321580	GTTTAAAGAACTGTC[C/T]GGCCGAGTCCCACAG	57674
rs80274947	snp	C/T	0.0298908	0.118541	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365185	CACCCGTGACCTTCA[C/T]GTGAGCACATCCAGA	57674
rs80276675	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80266278	GGAGCCCCATCTCTA[A/C]AAAAAAAAAAAAGAA	57674
rs80285607	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392618	GGGTTTTTTTTTTTT[C/T]TCGCTCTGTCGCCCA	57674
rs80322699	snp	A/C			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371951	TAACTGAAGATAAAA[A/C]TGAACTGTACATGCT	57674
rs80326542	snp	A/G	0.0475351	0.146656	intron-variant	RNF213	GRCh38.p7	17:80269821	CTACCTACATATTCT[A/G]TAGTTCTGCTCTCTG	57674
rs111164279	snp	G/T	0.331179	0.236453	intron-variant	RNF213	GRCh38.p7	17:80274903	TGTGTGTGTGTTGGG[G/T]GTGTGTGAGTGGGGT	57674
rs111171106	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313783	TACTGGAGGTGATGG[A/T]GGTGGTGAAGGTGAT	57674
rs111171107	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313831	TGATGGTGGTGGTGG[A/T]GGTGATGGTGGAGGT	57674
rs111171108	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313836	GTGGTGGTGGAGGTG[A/G]TGGTGGAGGTACTGG	57674
rs111171109	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313861	TACTGGAGGTGATGG[A/T]GGTGGTGAAGGTGAT	57674
rs111174326	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281347	ACGCCCCCACACACA[C/T]ACCCCACTCACACAC	57674
rs111174327	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281366	CCACTCACACACACC[C/T]CAACACACACACACA	57674
rs111174328	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281378	ACCTCAACACACACA[C/T]ACACCCCACTCACAC	57674
rs111211101	snp	G/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80274969	GGGTGTGTGTGTTGG[G/T]GTGTGTGTGTTGGAT	57674
rs111211103	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80313662	ATGGTTGTGGAGGTG[A/G]TGGTGGAGGTAATGG	57674
rs111211104	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80314343	ATGGTGGTGGTGGTG[A/G]TGGTGGAGGTACTGG	57674
rs111211105	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80315303	GTGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs111218667	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80313650	GTGGTGATGGTGATG[C/G]TTGTGGAGGTGATGG	57674
rs111218701	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315714	AGAGGTAATGGAAGT[A/G]ATGGTGGAGGTACTG	57674
rs111219133	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314334	ATGGAGGTGATGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs111219136	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314350	TGGTGGTGGTGGTGG[A/T]GGTACTGGAGGTGAT	57674
rs111219147	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80274814	TGAGTGGGGGGTGAG[G/T]GGGGTGTCTGTGGGG	57674
rs111219163	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315054	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs111219169	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314382	GCGGTCGTGGAGGTG[A/G]TGGTGGAGGTAATGG	57674
rs111219176	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314578	TGGTGGTGGTGGTGG[A/T]GGTGGTGGAGGTAAT	57674
rs111219190	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80314411	GGAGGTGGTGGTGGT[C/G]GTGGTGGTGGAGGTA	57674
rs111260266	snp	A/T	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320190	CCTCCTCCCCTCTAG[A/T]CACCCACTCCCCTCT	57674
rs111269189	snp	A/G	0.000214715	0.0103591	missense	RNF213	GRCh38.p7	17:80348104	GAGGAGGCCAAATCG[A/G]TCCTGCTGAACTGCG	57674
rs111270912	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80302117	GTAGAATAGTAGTTA[C/T]GAGAGGCGAGGAAGG	57674
rs111284234	snp	A/G	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387693	CCTCTCATGGCATAT[A/G]GGATAAAGCCGACAC	57674
rs111285069	snp	C/T	0.00041175	0.0143424	intron-variant	RNF213	GRCh38.p7	17:80343811	TAGAGTTGGGAGAAC[C/T]CGCCATCGTGTCGTG	57674
rs111303396	in-del	-/TTC	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80267826	AGATTTTCTTTTCTT[-/TTC]TTTTTTTTTTTGAGA	57674
rs111311825	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80280283	CCATGCGAGGAGAAG[A/G]AGGCTCGGGCTCAGC	57674
rs111321337	snp	C/T	9.89315e-05	0.00703249	synonymous-codon, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351739	TGAGGACCGTATCTT[C/T]GTCTATTTCATCACA	57674
rs111321460	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316814	GTGAAAGCAGCTGTG[C/T]GAAGCGTGAATCGCA	57674
rs111322810	snp	C/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80289060	GGATGGTCCCCGGAG[C/G]TGTCTGGGAAGGTCA	57674
rs111326764	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355791	GGGCTCATGGAGGAA[A/G]AAGCGGGGTGACCGG	57674
rs111336444	snp	A/T	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80273644	TTTTTTTTGAGACAG[A/T]GTTTCGCTCTTGTTG	57674
rs111338204	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385729	CACCCAGCACTGTGT[G/T]TGTTTGTTTTTGAGA	57674
rs111369726	snp	A/G	0.0136506	0.0814799	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288055	CTCTCCGCGCCCACC[A/G]AGGTTGGCGACAGCC	57674
rs111378555	snp	C/T	0.000805014	0.0200464	intron-variant	RNF213	GRCh38.p7	17:80337746	GCGGTCCCCAGCCCT[C/T]GGCGCAGCTGCGGCC	57674
rs111406243	snp	A/G	0.00369648	0.0428319	synonymous-codon	RNF213	GRCh38.p7	17:80348187	AGCGGAGTGGCTGTC[A/G]CAGGAGTACTTTCAC	57674
rs111424550	snp	G/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80265050	TGTTTGTTTGTTTTT[G/T]TTTTTTTTTTTAGAG	57674
rs111429617	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321851	CTGCCTCAGTCTCTC[A/G]AGTAGCTGGGACTAC	57674
rs111431858	snp	A/T	0.5	0	missense	RNF213	GRCh38.p7	17:80348205	GGAGTACTTTCACAG[A/T]CAGAGGCACAACTCC	57674
rs111440891	snp	C/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260298	TGCTGGGCGCCGGGG[C/G]GGGGGGCGCGCCTGT	57674
rs111463226	snp	G/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80265044	CTTCCATGTTTGTTT[G/T]TTTTTTTTTTTTTTT	57674
rs111478526	snp	A/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80280887	TGGAAACATTCCCAC[A/G]GAGTAACAGAGGCGC	57674
rs111488119	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357634	AGAGAACCTCGATGA[C/T]TTGTTCTGAAAAATA	57674
rs111492392	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80294323	AGTGATTGACCAGGA[C/T]AGTGCTCACTTGCTA	57674
rs111493114	snp	C/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391491	TGGCCAGGCTGGTCT[C/G]GAGCTCCTGACCTCA	57674
rs111501864	snp	G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355327	AAGCGGGGTGAACGG[G/T]AATGGGGGCTTACAG	57674
rs111524346	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80303092	AGGAAGTACTACTCA[A/C]GGCACAGCGTGTACA	57674
rs111525398	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80306930	ACATTTTTTGGTGGA[G/T]AAAATGGTATAAGTT	57674
rs111558064	snp	C/T	0.0364509	0.129988	intron-variant	RNF213	GRCh38.p7	17:80325989	TTGGAGATGGAGTCT[C/T]GCTCTCTCACCCAGG	57674

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