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
rs111571688	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80260964	ATACAGTGGGCCCCG[C/T]GGGCCGGCGGGCCGG	57674
rs111583546	snp	C/T	0	0	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351944	ACTACAACCTCAATC[C/T]CCTGGGTTCAAGCGA	57674
rs111591209	snp	A/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362932	ACACGGTGACCTTAA[A/C]GTGGGAGGAGAGGCA	57674
rs111591237	snp	C/G	0.0166325	0.0896639	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364937	AGTCATGGAGACAAG[C/G]ATGTCAGAGAATGCC	57674
rs111591291	in-del	-/T/TT	0.459801	0.135955	intron-variant	RNF213	GRCh38.p7	17:80331390	TTGTCAGTTTATGAC[-/T/TT]TTTTTTTTTTTTTTT	57674
rs111601823	snp	A/C/T	0	0	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383861	TTACAGTTGAGTACC[A/C/T]CCAGCACATTGTGGA	57674
rs111604394	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80340609	GCAGTGTACTTTGTG[G/T]TTTTTTTTTTTTTTT	57674
rs111634655	in-del	-/ATAAC	0.363985	0.222503	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396274	TCAAAAAAAAATAAA[-/ATAAC]ATAAGGACCTTATTG	57674
rs111640038	in-del	-/GT	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80275070	GTGTGTGAGTTGGGG[-/GT]GTGTGAGTGGGGTGT	57674
rs111659420	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80307239	TCTCTCCCTCACATG[C/T]GGCCCCCGGGGGCTT	57674
rs111671408	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80312954	GGGGTGCAGCATCTC[A/G]CCGGGAACCTGAGTC	57674
rs111685972	snp	C/T	0.000312956	0.0125052	missense	RNF213	GRCh38.p7	17:80344880	ACCAAGACCTAGACA[C/T]GTTTCAGTATCAAGA	57674
rs111691875	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358692	GAGGCAGGTGGATCA[A/C/T]GAGGTCAAGAGATCA	57674
rs111743102	snp	A/G	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80334913	TTACAGGCATGAGCC[A/G]CTGCACCTGGCCTTT	57674
rs111751548	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80279342	GGGCCCGACCCAGCC[C/T]CTGCCTGAACACAAG	57674
rs111754394	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80272906	GGGAGGAAAGCGTAA[C/T]AGGCTCTGTTTTAGA	57674
rs111760060	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80292424	CAGAAGAAGGGCTGC[A/G]GCTGGGAACAGAGGG	57674
rs111771227	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351999	AGCTGGCATTACAGG[C/T]GTGCGCCACCATGCC	57674
rs111773570	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80277348	CTCACCTGTAATCCC[A/G]GCACATTGGGAGGCT	57674
rs111776620	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80282283	TTGTTATTGTTGTCT[C/T]GTTATTTTCTGTTTT	57674
rs111808834	snp	A/T	0	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393939	TCTTCCATTCCCTTA[A/T]ATTCTGAGTACTGTA	57674
rs111823869	snp	C/T	0.0558544	0.157504	intron-variant	RNF213	GRCh38.p7	17:80305288	GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC	57674
rs111829552	in-del	-/GTGCATGC	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379043	CAGCAGGGCATGGTG[-/GTGCATGC]GTGCATGCGTGCATG	57674
rs111847477	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80349721	TGGCAGCAGACTTGC[A/G]ACCTTTCCTTGAAGT	57674
rs111890277	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80301923	AAGAAAGTGTTGTCT[A/G]TATACACAGTAGAAT	57674
rs111893179	snp	C/T	0.0174175	0.0916809	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373637	CTTGCAAGGTGCGAC[C/T]TTTTTACCTCTGGCA	57674
rs111901869	snp	A/C/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355360	GAAGAAGCGGGGTGA[A/C/G]CGGGAATGGGAGCTT	57674
rs111904941	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371235	TGCAACTAACCTCTA[C/G]ACATGACCATTTATC	57674
rs111905808	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378817	CTCAGTATATTGTGG[C/T]ACAATATCTGATTTT	57674
rs111908723	snp	A/C	0.0337553	0.125452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386552	TCCTTCAGCCGCCCC[A/C]ACCAGTGACCCGCCC	57674
rs111932036	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80293767	GGGAGGCGGAGCTTG[C/T]AGTGAGCCAAGATCG	57674
rs111939286	in-del	-/GGAACGT	0.199873	0.244923	intron-variant	RNF213	GRCh38.p7	17:80284710	CTCTGCCTTCCGGAC[-/GGAACGT]GGCTCCCCCACTGAG	57674
rs111951462	in-del	-/CTAAGCCTCCTT	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80308449	CCTCCTGAGTCCCTC[-/CTAAGCCTCCTT]CTGAGTCCCTCCTAA	57674
rs111971327	snp	C/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281615	ACAGCCAACTCACAC[C/G]ACTCACACACACCCC	57674
rs111992928	in-del	-/AC	0.257454	0.249889	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371767	TATGTATATGTTTAT[-/AC]ACACACACACACACA	57674
rs112002385	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80310295	TTTGCTCTTGTTGCC[A/C]AGGCTGGAGTGTAGT	57674
rs112002823	in-del	-/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355671	GGGAATGGGGGCTTA[-/C]AGGGGGAAGAAGCGG	57674
rs112003608	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80333823	AACAGTAGTTACTTG[A/G]CAGGGTTATGTGAGG	57674
rs112004708	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352037	TTTTTGTATGTTTAG[C/T]AGTGACGGGGTTTCA	57674
rs112005182	snp	C/T	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80297428	GCACTCCAGCCTGGG[C/T]GACACAGTGAGACTT	57674
rs112007394	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280900	ACGGAGTAACAGAGG[C/T]GCGACCTGGGGATGC	57674
rs112015622	snp	A/C	0.00128683	0.025333	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361728	TCCTTGGTTTCCTCT[A/C]TGCAGGACTGCCCAA	57674
rs112032495	snp	A/G	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80297545	GGATTGCTTGAGCCA[A/G]GAGTTCAGGATCAGT	57674
rs112052490	snp	A/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369744	GTCTCATGCAGTGAG[A/C]TGCCTTTTTCTTTCT	57674
rs112085363	snp	A/C/T	0.00358891	0.0422285	intron-variant	RNF213	GRCh38.p7	17:80281075	CCCCAGTCACACACA[A/C/T]CCCCCGCCACACATA	57674
rs112089914	snp	C/T	0.00129228	0.0253864	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288129	AAGTGAGGCTCAGAG[C/T]AGCCCGCAATTCCAG	57674
rs112107562	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80268381	AAAAAAAAAAAAAAG[A/G]CAGTACTGCATCCCC	57674
rs112152354	snp	A/G	0.029116	0.117091	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396348	GTGCATGTGTTAACC[A/G]AGACGGCCCTGAGCT	57674
rs112156875	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359864	TTTGCCTGTGAAACA[A/G]AGATTGCATAAGACA	57674
rs112158440	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80308389	CTCCTCCTAAGTGTC[C/T]TCTTAAGTCTCTCCT	57674
rs112159580	snp	C/T	0.0174175	0.0916809	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373902	CAGCTAGTCGGGAGG[C/T]TGAGGCAGGAGAATC	57674
rs112163422	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80302784	AGGATCGCTTGAGCC[A/C]GGGAGGTCAAGGCTG	57674
rs112173371	in-del	-/T	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80330606	CATCCTCCTTCCCCC[-/T]GAGATTGGATAATTC	57674
rs112178350	in-del	-/A	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80293666	GTCTCTACTAAAAAT[-/A]CAAAAAAATTGGCCG	57674
rs112182063	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259690	CTAATTTTTTTAAAT[G/T]ATTTTTTTTGTAGAG	57674
rs112185589	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80280916	GCGACCTGGGGATGC[A/G]CACGGAGCATGAGAT	57674
rs112186995	snp	C/T	0.444444	0.157135	intron-variant	RNF213	GRCh38.p7	17:80263340	CCCTGCCGAACAGCA[C/T]GTGGCTGCCCCACGC	57674
rs112188690	snp	C/T	0.0429648	0.14013	intron-variant	RNF213	GRCh38.p7	17:80303849	TGCTGGGATTACAGG[C/T]GTGAGCCACCCACTG	57674
rs112199238	snp	C/T	0.029116	0.117091	intron-variant	RNF213	GRCh38.p7	17:80351169	AAGGGAATGGCATTG[C/T]GCACAGAACTCTTTG	57674
rs112205049	snp	A/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390535	CCAAATAGCTGGGAC[A/T]ACAGGCGTGTACCAC	57674
rs112206282	in-del	-/G	0.214843	0.247516	intron-variant	RNF213	GRCh38.p7	17:80266428	TAGAAGAAAAGAAAA[-/G]GAAAAAAAAAGCCTT	57674
rs112208381	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80306818	GATCACGCCGCTGCA[A/C]TCCAGCCTGGGTGAC	57674
rs112213789	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80342741	ATATATATTATATAT[A/T]TATTGTATGTATATA	57674
rs112264422	snp	A/G/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80290403	TGCGTGTACGTGTGC[A/G/T]TGTGTGTGTGCGTGT	57674
rs112299691	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80305427	AGGTGATCTGCCTGC[C/T]TCGGCCTCCCAAAGT	57674
rs112305796	snp	A/G	0.000214513	0.0103542	synonymous-codon	RNF213	GRCh38.p7	17:80343187	GATGCAGTTAAACGT[A/G]AAAAATGTGCCTCTG	57674
rs112324637	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80282277	TGTTCTTTGTTATTG[C/T]TGTCTCGTTATTTTC	57674
rs112328633	snp	C/T	0.0174175	0.0916809	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372892	GCCTGTGGGTAGGTC[C/T]GATGCCCTCTGGTTG	57674
rs112351624	snp	A/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80301575	AATTAGGGAAATGCA[A/T]ATCAAAACCACAATG	57674
rs112392725	in-del	-/AAAAC	0.190519	0.242821	intron-variant	RNF213	GRCh38.p7	17:80284380	AAAAAAACAAAAACA[-/AAAAC]AAAACAAAACAAAAA	57674
rs112395903	snp	A/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80318860	TGACAGGCGTGAGCC[A/T]CCGCGCCCGGCCTAT	57674
rs112401479	snp	A/G	0.00460056	0.0477401	missense	RNF213	GRCh38.p7	17:80348062	GGTCCCCGGGCCTTG[A/G]CGGAGGAACTTCACC	57674
rs112405629	snp	A/G	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364956	TCAGAGAATGCCACC[A/G]GGGTTTGGGGTCTTC	57674
rs112414094	snp	C/T	0.00557542	0.0525036	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320609	TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA	57674
rs112421902	snp	A/G	0.5	0	missense	RNF213	GRCh38.p7	17:80345053	TGCAATCCGAGTTTT[A/G]TTGGCGACACACTGA	57674
rs112433476	snp	C/T	0.000297064	0.0121838	intron-variant	RNF213	GRCh38.p7	17:80291582	AATAACTAAAATTTC[C/T]GGGGTAGGAATTTTG	57674
rs112438520	snp	C/T	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396376	GCTATTTCAGTTACT[C/T]CTGTATGTTCAGGCA	57674
rs112452061	snp	A/C	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80280509	CCCAGGCTGGAGCGC[A/C]GTGGCAAAATCATAG	57674
rs112460310	snp	C/T	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364850	ACCTTCGGCAGGGAT[C/T]ACCTGGCCTTTGGAG	57674
rs112467413	snp	C/T			splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374591	AGACTGCTCTGAAGG[C/T]AGGATGGGCCCGTGG	57674
rs112467895	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80277066	CTCTCAAAACAAAGC[A/G]AACAAACCAAAAAAA	57674
rs112470698	snp	A/T	0.0123036	0.0774623	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259693	ATTTTTTTAAATGAT[A/T]TTTTTTGTAGAGATG	57674
rs112496479	snp	G/T	0.444444	0.157135	intron-variant	RNF213	GRCh38.p7	17:80326806	ACCCGTTCACCTCAT[G/T]AAAGACATCTTGGTT	57674
rs112508603	snp	A/C	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281606	CCAACACACACAGCC[A/C]ACTCACACCACTCAC	57674
rs112535386	snp	C/T	0.105291	0.203861	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376983	GTGTTGGGGTCTAGA[C/T]GACCCCACACTCCTT	57674
rs112540534	snp	A/C	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355803	GAAAAAGCGGGGTGA[A/C]CGGGAATGGGGGCTT	57674
rs112576397	snp	C/T	0.5	0	synonymous-codon	RNF213	GRCh38.p7	17:80346577	GCCAAGAACTTGGCC[C/T]TGAAGGAGAACGTCT	57674
rs112581808	snp	C/T	0.0573587	0.15934	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390254	GTGCTGTCTCTCCTG[C/T]GATCTTCTATAGACA	57674
rs112589147	snp	A/G	0.0248432	0.108648	intron-variant	RNF213	GRCh38.p7	17:80293720	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	57674
rs112597118	snp	A/G	0.331411	0.236373	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261121	CCCGGCTGCGGGAGG[A/G]GTCGGGGTGGGGGCA	57674
rs112599480	snp	A/G	0.148661	0.22854	intron-variant	RNF213	GRCh38.p7	17:80305889	CCTCCCAAAGTGCTG[A/G]GATTCAGGCGTGAGC	57674
rs112599521	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274614	GGGGTGAGTGTGGGG[A/G]GTGAGTGGGGTGTCT	57674
rs112602766	snp	A/C/G/T	0.000971457	0.0220184	synonymous-codon	RNF213	GRCh38.p7	17:80290573	GTTTTCCACCAGCAC[A/C/G/T]CTGAGCCCGGGTGGA	57674
rs112612767	snp	G/T	0.189261	0.242509	intron-variant	RNF213	GRCh38.p7	17:80299747	AAGCCCCAGTGTGTG[G/T]TGTTCCCCTCTATGT	57674
rs112619664	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383195	GCCTTTGACTGAGCC[C/T]CAGATTCCAATGCTC	57674
rs112648102	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80277603	TCTGTCTCAAAAAAA[A/T]AAAAAAAAAAAAAAG	57674
rs112649406	snp	A/G	0.184203	0.241186	intron-variant	RNF213	GRCh38.p7	17:80303625	CTGGAGTACAGTGGC[A/G]CGATCTCTGGTCACT	57674
rs112658337	snp	A/G	0.0205511	0.0992634	intron-variant	RNF213	GRCh38.p7	17:80297190	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	57674
rs112658451	in-del	-/TT/TTTTTT	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80265040	GTCCTTCCATGTTTG[-/TT/TTTTTT]TTTGTTTTTTTTTTT	57674
rs112668861	in-del	-/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80308348	ACACCGCCTTCCCAG[-/T]CCCCTCCATCAACTC	57674
rs112694099	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355675	ATGGGGGCTTACAGG[A/G]GGAAGAAGCGGGGTG	57674
rs112706267	snp	C/T	0.0221141	0.102801	intron-variant	RNF213	GRCh38.p7	17:80273821	GACGGGGTTTCACCA[C/T]GTTGGTCAGGTTGGT	57674
rs112723210	snp	C/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80336817	GCTGAGACAGAATTG[C/G]TTGAACCCGGGAGGC	57674
rs112735431	snp	A/C/G	0.000741076	0.0192355	RNF213, LOC100294362	17	allele_origin=G(germline)/A(germline)	17:80385145	AATACAGCTCCATCA[A/C/G]AGGCTTCCTCAGCAA	57674
rs112745679	snp	A/G	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80279185	TTGCCTTTTTACTCC[A/G]TGCAGCTGTCCCCTT	57674
rs112752694	snp	G/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80265045	TTCCATGTTTGTTTG[G/T]TTTTTTTTTTTTTTT	57674
rs112756191	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80290835	TTTTTTCTGAGACGG[A/G]GTCTTGCTGTGTCAC	57674
rs112760467	snp	A/G	0.0952156	0.196321	intron-variant	RNF213	GRCh38.p7	17:80298802	AAAACCCGTCTGTAC[A/G]AAAAATACCAAAAAA	57674
rs112762659	in-del	-/AT	0	0	intron-variant	RNF213	GRCh38.p7	17:80342734	ATGTATATATATATT[-/AT]ATATATATATTGTAT	57674
rs112785491	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357036	GCGATTCTCCTGCTC[A/G]GCCTCCTGAGTAGCT	57674
rs112788786	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358852	AGGCGGAGGTTGCAG[C/T]GAGCCGAGATGGCGC	57674
rs112791875	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375215	TGGCTGCTAAATATG[C/T]GTTGAGTTTAATCTG	57674
rs112814742	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80280441	AGTATAGCTCTGAAT[A/G]GGTTTGGTGGGTTTT	57674
rs112816799	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80302820	GTAGAAGTCCAGATT[C/T]CCTAGAAGTTGAAAT	57674
rs112831272	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80297013	CAACCAAATAAACGC[C/T]GCACATTTTGACAAA	57674
rs112840686	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355852	TGAACGGGAATGGGG[A/G]CTTACAGACACCTTC	57674
rs112850201	snp	C/T	0.0205511	0.0992634	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321567	TCCATGTTTAATTGT[C/T]TAAAGAACTGTCCGG	57674
rs112876212	snp	C/T	0.0283406	0.115616	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386188	CATCCCTCCTCCCCA[C/T]GCCTAGATTCTGTGA	57674
rs112888599	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355334	GTGAACGGTAATGGG[A/G]GCTTACAGGGGAAGA	57674
rs112893661	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369926	TTCTCTTCATCGCAG[C/T]GTTTTGTTACCAAGT	57674
rs112896558	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355560	GGGAATGGGGGCTTA[C/T]GGAGGAAGAAGCGGG	57674
rs112897174	snp	A/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351916	CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT	57674
rs112918888	snp	A/C/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80263488	GGGGCAGCACAGAGC[A/C/G]GGGAGGGGCTGGGCT	57674
rs112927547	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80270160	TGCCCTGCGCATGCC[A/T]TGCTACTTTCATGTA	57674
rs112937465	snp	A/G	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80330105	TTCATGTCAGCTTTC[A/G]TATATATATTTAATG	57674
rs112946552	in-del	-/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80328588	GAGAAGGCTTTAAAA[-/T]TTTTTTTTTTAATTT	57674
rs112950687	snp	G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389094	GCTTGGGCAGTGAAG[G/T]GGCTCGGCTCTCTTA	57674
rs112962305	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349610	CGGCCCCAGCGCTGC[A/C/T]GTGTTTTGGGAAACT	57674
rs112975996	in-del	-/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80333066	TGCTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	57674
rs112998778	snp	A/T	0.000167001	0.00913633	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390200	CCCTCAGTGGAGGTA[A/T]GGATTTGCACACCTA	57674
rs112999459	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80351002	TATTTTTATAGTGTT[C/T]GTAGGGGAAGTCTGA	57674
rs113004646	snp	A/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80273916	TGAGCCACCGCGCCC[A/G]GCCTCCACCTTCCTT	57674
rs113009753	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315891	GGAGGTGATGGTGGT[A/G]GTGAAGGTGATGGTG	57674
rs113011315	snp	A/G	4.70079e-05	0.00484786	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353527	TGGGCTTGGAACACC[A/G]GGCGGAAGACGGCCA	57674
rs113032585	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80280656	GATGGGGTCTTGCTG[C/T]GTTACCCACGCTGGT	57674
rs113038654	snp	C/T	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396726	CCAGGAAAGTGCATT[C/T]CCCCCCCACCCCCCC	57674
rs113042505	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80331632	GACCTCAGGTGATCC[A/G]CCCATCTCAGCGTCC	57674
rs113058018	snp	A/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80272668	TTGGTGGGGATGGAC[A/G]AAGTGCGTCCACACC	57674
rs113060724	snp	A/G	0.5	0	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376358	CTTTCACCTCCTGAT[A/G]TCAGCCGTTTTGCAA	57674
rs113066160	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379504	AAGCACACACTGGGA[C/T]AATCTGAGGGTGCTC	57674
rs113073385	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80296084	GAGTACAGTGGCGCA[A/G]TCTTGGCTCACTGCA	57674
rs113077984	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80284078	AAATATGAAAATTAC[A/G]GCCGGGCACAGTAGC	57674
rs113096037	snp	A/G	0.5	0	synonymous-codon	RNF213	GRCh38.p7	17:80291739	TGGGGAATCTTTTGA[A/G]TATGAGTTCATTTAC	57674
rs113098098	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382315	TGGTTATCTGTGAGT[G/T]GTGGAATTAAGAGTG	57674
rs113098281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308184	GAGCTGTTCTCTGAG[C/T]GGCTCGGGCACTTCC	57674
rs113122692	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260156	TCCGCGCGGGGCCGC[C/G]GAGGTCCCTTAATCT	57674
rs113139767	snp	A/G	0.00398882	0.0444803	missense	RNF213	GRCh38.p7	17:80334117	CAGACTGATAACTTC[A/G]ACGACTTTCGCCGTG	57674
rs113139900	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80322020	TGAGCCACTGTGCCC[A/G]GCCTCATTGTGGTTT	57674
rs113143156	snp	A/G	0.5	0	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320045	TTGTTCGTATGCCAT[A/G]CGGTACATCTGTCAA	57674
rs113156040	snp	C/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80349492	TGAGAATCTCAAGTA[C/G]GGACCAAGCAGGCAG	57674
rs113156418	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360680	CCCAGCTGTGTCTCC[C/T]GAGTCACAGCCCAGA	57674
rs113159878	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353790	GGGTGAGGATGGCGC[C/T]CCACTTTCCTCACAC	57674
rs113174770	snp	G/T	0.0524604	0.153226	intron-variant	RNF213	GRCh38.p7	17:80334625	AGAGAGGTTTTTTTT[G/T]TTTGTTTGTTTGTTT	57674
rs113179528	snp	C/T	0.104149	0.203046	intron-variant	RNF213	GRCh38.p7	17:80265184	CCCAAGTAGCTGGGA[C/T]TACTGGTACCCACCA	57674
rs113198440	in-del	-/AC/CA	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371768	ACACACACACACACA[-/AC/CA]GGACAGACGACCGAT	57674
rs113231386	snp	C/T	0.5	0	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396680	CAACCATTACCATTA[C/T]GAATCCCGTTTCCAG	57674
rs113236556	snp	C/T	0.0967359	0.19751	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376288	TCTTAATGTTAAGTT[C/T]TTTTCCTGTCAGCAA	57674
rs113247758	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386123	CAGCATATGAGATGG[A/G]GCAGAACCGAGACCC	57674
rs113259603	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80323514	AGGTTAAGTTGGATT[C/T]CTTTCATTCAATTAG	57674
rs113261807	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80298643	ACAGAACTAACACAC[A/G]CTCTTTTAACATTTT	57674
rs113346223	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80291078	AGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT	57674
rs113376734	snp	C/T	0.5	0	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381654	GCTGGGACACAGTGC[C/T]GACGAGACCATCGGC	57674
rs113392257	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369969	ACTAGTAGCTAGTAC[A/G]TGATCTTGGGGAGCT	57674
rs113392751	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80386024	CTGGATAAGTAAAAT[A/G]ATGTGTCAGGAAAAT	57674
rs113402224	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80279994	CAGCCCCTGCCCATC[A/G]AGATGGTCATGTGTT	57674
rs113411478	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355767	AAGAAGCGGGGTGAA[C/T]GGGAATGGGGGCTCA	57674
rs113422455	snp	A/C	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80331163	CAGTCTTCCTTATTT[A/C]ATCACCACCTCCCAG	57674
rs113428316	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356190	TATTTTTAGTAGAGG[C/T]GAGATTTCACCATGT	57674
rs113442952	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80317109	GTATTGCCGTAATGC[C/T]CTGTCTTTCTCCTTT	57674
rs113445262	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391642	CTCTGCCGTGTGCCA[C/T]AGTGCTCTATTTCAG	57674
rs113482971	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386547	CTCACTCCTTCAGCC[A/G]CCCCCACCAGTGACC	57674
rs113485769	snp	G/T	0.0659589	0.169201	intron-variant	RNF213	GRCh38.p7	17:80325408	ACAGCCACTATTCAT[G/T]GAATGCTTGCTGTAC	57674
rs113488846	snp	A/G	0.5	0	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288712	AGACCCAGAGAATGA[A/G]ACAGCCACCAGCAAC	57674
rs113523225	in-del	-/A	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80338948	GCAAGACTCCATCTC[-/A]AAAAAAAATTAAAAA	57674
rs113530384	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363030	GTTTTCCAATAGTTC[A/G]GATTTCCCACGGGGA	57674
rs113540778	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80281636	CACACACCCCCAACA[C/T]ACACTCCCCACTCAC	57674
rs113543071	snp	A/G	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80342982	GGCTAATTTTTTTGT[A/G]TTTTTAGTAGGGACG	57674
rs113543920	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80293990	CAACTGTGGGTCGAA[A/G]GCATGGCAGGGGGCT	57674
rs113550121	snp	A/T	0.5	0	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321182	AATTCACTTGTTTCA[A/T]ATACATCTTATACAC	57674
rs113560699	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276895	GTCTCTACTAAAAAT[A/G]CAAAAAAAAAAATTA	57674
rs113560778	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80263107	TTTGATGCCATCCAC[C/T]GCAGAGGCTGTTCTG	57674
rs113572620	snp	C/T	0.5	0	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259560	TGAGGCAAGATCTCA[C/T]TTTGTCATCCAGGCT	57674
rs113585495	snp	A/T	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379015	CCCGTCTCTACAAAA[A/T]AACACAAAGCATCAG	57674
rs113599364	snp	A/G	0.0126979	0.078662	intron-variant	RNF213	GRCh38.p7	17:80318764	ATTTTTTGTAGAGAC[A/G]GGGTTTCACCGTGTT	57674
rs113613506	snp	A/G	0.0295035	0.117819	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387899	GCAGTCATATCTACT[A/G]TACTTATGTACGGTA	57674
rs113614776	snp	A/G	0.00499304	0.0497151	missense	RNF213	GRCh38.p7	17:80273246	GCCGTTACAGATTCT[A/G]AGAACAATAACTCCA	57674
rs113614977	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80262820	CAGTGGGAGGAGAGG[A/G]CAGGGCCAGGGCAGG	57674
rs113622765	in-del	-/TA	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80324710	TTTATTCATTTTTGG[-/TA]TTTTTCATGATATGA	57674
rs113635998	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80308845	TTTGCTTCCTTTTTA[C/T]CTTAGTCACAAGTTC	57674
rs113637172	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372050	ACATGGTTTAAAATT[C/T]ACAGAATATAATTTT	57674
rs113639358	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388953	GAAGTCCATGGAACC[A/G]ATTTGTTCCTGCTCT	57674
rs113653790	in-del	-/AAA	0.040671	0.13668	intron-variant	RNF213	GRCh38.p7	17:80304656	AATAAATAAATAAAT[-/AAA]TAATAATAATAATAA	57674
rs113654628	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80303327	GGCCTTGCAGTGAGA[A/G]CAAGACAGTGACCAT	57674
rs113656240	snp	C/T	0.000115625	0.00760258	missense	RNF213	GRCh38.p7	17:80347913	TGGAGGAGCTCTGTG[C/T]GTGGGTGGAGAAGTT	57674
rs113715964	snp	G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355741	TGGACGGGAATGGGG[G/T]CTCACGGAGGAAGAA	57674
rs113718186	snp	C/T	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80279550	GTTCACTGCAACCTC[C/T]GCGTGCAGGGTTCAA	57674
rs113718409	snp	A/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80275756	CAACCTTTGCCTCCC[A/G]GGTTCAAGTGATTGT	57674
rs113721370	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80266472	AGTGCTCAAATGAAA[A/C]GTCTCTTGCCTCTCA	57674
rs113739240	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80282089	TTCAAGCTCCTGACC[C/T]CAAGGAATCCGCCTG	57674
rs113759108	snp	A/G	1.64798e-05	0.00287047	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319378	TGCCATGACCCAGCT[A/G]AGGGCTATGAAGCAC	57674
rs113762139	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355781	ATGGGAATGGGGGCT[C/T]ATGGAGGAAAAAGCG	57674
rs113777066	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80284915	TCCCCCAGTGGGTCC[C/T]TATGGCCAGGATGAT	57674
rs113778434	snp	C/T	0.0205511	0.0992634	intron-variant	RNF213	GRCh38.p7	17:80311684	CCTCTCTCCCACTCT[C/T]GGGCAGCCCCGCCCA	57674
rs113780630	snp	C/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365313	TGTGTTGACTCTGAC[C/G]TATCAAAACATCAGC	57674
rs113786252	snp	A/G	0.155325	0.23138	intron-variant	RNF213	GRCh38.p7	17:80304551	AGGCTGAGGCAGGAG[A/G]ATGGCGTGAGCCTGG	57674
rs113790473	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80341870	GGAGTGCAATGGCAC[A/G]ATCTCGGCTCACTGC	57674
rs113795597	snp	C/T	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80311701	GGCAGCCCCGCCCAG[C/T]AGCAGCCTTGTCCTC	57674
rs113797807	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80343639	GAGCCAATTGTAAAA[C/T]GGTGTATTTATGTGT	57674
rs113801645	snp	C/G/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355746	GGGAATGGGGGCTCA[C/G/T]GGAGGAAGAAGCGGG	57674
rs113809573	snp	C/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80268980	CTGAAGACCCGAGAT[C/G]CCCCTGGCAAACCAC	57674
rs113812806	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80318331	GGCTTTTCGGCTCGA[A/G]GGTGGGGTTTTGCCA	57674
rs113817905	in-del	-/TCTC	0.5	0	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259712	TTTGTAGAGATGGGG[-/TCTC]TCTATGTTGCCCAGG	57674
rs113829711	snp	C/T	0.0314385	0.121371	intron-variant	RNF213	GRCh38.p7	17:80292077	ACTTGCAGGAGGAAA[C/T]ATGCAAAGGACTTTT	57674
rs113835001	snp	C/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379208	ATAAAAATTGATATA[C/T]GAAAAAGTCCAAATG	57674
rs113836304	snp	A/G	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382038	AGTGTGCATATATGG[A/G]GAGTCTTCAGTTCCG	57674
rs113898106	in-del	-/TCTA	0	0	intron-variant	RNF213	GRCh38.p7	17:80268645	CCATCCGTTTATCTG[-/TCTA]TCTATCTATCTGTCA	57674
rs113899492	snp	A/G	0.000242537	0.0110095	intron-variant	RNF213	GRCh38.p7	17:80317294	TACCAAAAGTTTGGG[A/G]GCAGTCTTTTCAGGG	57674
rs113926535	snp	C/G/T	5.12197e-05	0.0050604	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383083	GAGGTAAGCAGTAAG[C/G/T]GCTGACAGCTGGGTT	57674
rs113957515	snp	C/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80290452	GTGCATGTGTGTGTG[C/T]GAGTGCATGTGTGTG	57674
rs113970647	snp	A/G	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80271877	CCCAGCTACTCCAGA[A/G]GCTGAGGCAGGAGAA	57674
rs113976037	snp	A/C	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378271	GCATTATTAGCCCTC[A/C]GAGGAGGTGTGGTCC	57674
rs113980279	snp	A/G	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80304504	AATGAGCCGGGCGTG[A/G]TGGCAGGCGCCTGTA	57674
rs114014180	snp	C/T	0.00294071	0.0382323	synonymous-codon	RNF213	GRCh38.p7	17:80346765	GTCCTTCCAGTGCAG[C/T]CCGCACTCCACCCCA	57674
rs114046339	snp	A/G	0.001233	0.0247988	splice-acceptor-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351683	TTTTTTTCTTTAAAT[A/G]GGTATTCTGTTATAA	57674
rs114047543	snp	A/G	0.0031973	0.0398551	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380812	CAGCCTCTGTCTTGT[A/G]TTCTCTCGTTCTTTC	57674
rs114066464	snp	A/C/G	0.00304505	0.0389011	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288391	GGAGAGATGGCCTGG[A/C/G]AGTGGCACTGAGCCC	57674
rs114066952	snp	A/G	0.0681886	0.171594	intron-variant	RNF213	GRCh38.p7	17:80318220	GTTTTGGAAAAAGCA[A/G]CATTCTATTGGTAAA	57674
rs114076467	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281231	CCCCACACACACCCC[A/C]CTCACACACACCTCA	57674
rs114101754	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80324468	TAACATGGGGCTGGA[C/T]AAGGTTTTCTTTTAT	57674
rs114109468	snp	C/T	0.0479149	0.147179	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372264	TACTTTTTATCTTCA[C/T]ATTTTTATATCCAAA	57674
rs114138189	snp	A/G	0.0279526	0.114869	intron-variant	RNF213	GRCh38.p7	17:80283780	GGGCTGTGACTCGGC[A/G]GTCCAGAGCCTCAGG	57674
rs114144279	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322352	AAATTTCTGTGGGCC[A/G]GGCATGGTGGCTCAT	57674
rs114161078	snp	C/T	0.0193772	0.0965046	intron-variant	RNF213	GRCh38.p7	17:80297820	ATGTAGCTAGCTGGG[C/T]GTGGTGGTGCACCTG	57674
rs114234895	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274882	GTGTGAGTGGTGTGA[A/G]TGGGATGTGTGTGTG	57674
rs114259795	snp	A/G	0.0024038	0.034585	synonymous-codon	RNF213	GRCh38.p7	17:80346315	CGCGATGCTCTTAGC[A/G]CAGCTGAATGCCTTT	57674
rs114281567	snp	A/G	0.00557542	0.0525036	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364369	CCCGTCTCCCTCCTC[A/G]TTTCACCCTTGGGTT	57674
rs114331720	snp	C/T	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360822	TCCACGTTTACTTAT[C/T]GTACCATTTGGAAGA	57674
rs114333705	snp	A/G	0.00335498	0.0408195	missense	RNF213	GRCh38.p7	17:80343962	TGCCATTTGTATATC[A/G]TTGAAATCCTGGAAA	57674
rs114341790	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80350980	GCTTTTTTTCCTATT[C/T]ATTGGATATTTTTAT	57674
rs114346289	snp	A/G	0.0486741	0.148216	intron-variant	RNF213	GRCh38.p7	17:80310241	GATGTAAGGTTTAAT[A/G]TTTAGACTGATCATT	57674
rs114349828	snp	A/G	0.0622301	0.165053	intron-variant	RNF213	GRCh38.p7	17:80331726	TGCAATTTATGTTCT[A/G]TCATTGGAGTGGGGT	57674
rs114352301	snp	C/T	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80306580	ACAGTGGGCTGGGTG[C/T]GGTGGCTCACGCCTG	57674
rs114370278	snp	A/C/G	0.0033946	0.0410587	synonymous-codon	RNF213	GRCh38.p7	17:80348253	GGCACACCTGCACAC[A/C/G]GCAGACCTGGAGCGC	57674
rs114386297	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80343512	GTGTGAACGTCATGG[C/T]GTGCGCTTACACTAA	57674
rs114393774	snp	G/T	0.0166325	0.0896639	intron-variant	RNF213	GRCh38.p7	17:80263549	CCAGGGGACCAGCTG[G/T]GCTGCTGTGATTTCA	57674
rs114454593	snp	C/G	0.00380061	0.0434265	missense	RNF213	GRCh38.p7	17:80289696	ACGAGATGGCTGCTG[C/G]TGAAGAAAAAGTCGG	57674
rs114493717	snp	A/G	0.00347155	0.0415177	missense	RNF213	GRCh38.p7	17:80273288	GCCTCGGAGGGTGAA[A/G]TGGAGTGTGGGCAGG	57674
rs114527357	snp	A/G	0.030665	0.119967	intron-variant	RNF213	GRCh38.p7	17:80317766	CGTCTATGGACAGTA[A/G]TGTGTTATCAGCTCA	57674
rs114541994	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281589	ACACCACTCACACAC[C/T]GCCAACACACACAGC	57674
rs114546296	snp	A/G	0.0629771	0.165899	intron-variant	RNF213	GRCh38.p7	17:80336826	GAATTGCTTGAACCC[A/G]GGAGGCAGAGATAGC	57674
rs114614326	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281526	ACCCCAACACACACA[C/T]GCCCCACTCATACCA	57674
rs114631389	snp	A/G	0.0441095	0.141807	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387043	TCCCGAGGCCACCAC[A/G]CCACCTGTATCTCCG	57674
rs114644643	snp	C/T	0.0170251	0.090679	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395495	GACTTTTCCTCTGGA[C/T]AAAATGACAGCATCC	57674
rs114649707	snp	C/T	0.000362821	0.013464	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388700	CACAGGTGATCCCGA[C/T]AAACCTGATCCTGTG	57674
rs114650825	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281487	ACACACCCCCCAACA[C/T]ACATACACCCCACTC	57674
rs114683850	snp	G/T	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356315	CCTGTTGATGCTTTT[G/T]AATCCCTGACTCCAC	57674
rs114693734	snp	A/G	0.00102118	0.0225732	missense	RNF213	GRCh38.p7	17:80345995	ATGGAGGAGACGGCC[A/G]ACAGGCTGGGCTCCA	57674
rs114736392	snp	G/T	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80271074	TCGGCCCTGATTGGA[G/T]TAGGCTAGTCAGGGC	57674
rs114740256	snp	A/G	0.0314385	0.121371	intron-variant	RNF213	GRCh38.p7	17:80283365	CAGATGGTTGGTTTT[A/G]TTTCTATTGAAAAGA	57674
rs114745496	snp	A/G	0.0158469	0.0875917	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367272	TTATCTCTGGGGAGG[A/G]ACGGAGGGATGTGAA	57674
rs114748029	snp	A/G	0.0103295	0.0711199	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351551	AAAACTCATCGGAAC[A/G]GGTGGCCGTGAGACC	57674
rs114749972	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392591	GACCTTAAACTGCTC[C/T]TCAGGATTTCTGGGT	57674
rs114810103	snp	C/G	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387549	GCCAAAGCCCACCCT[C/G]TAGTTAAAAGCATCC	57674
rs114816446	snp	C/T	0.00132461	0.0257012	synonymous-codon	RNF213	GRCh38.p7	17:80346483	TCCGAAACCGTATGA[C/T]GACAGCAGGCTGCTT	57674
rs114819492	snp	C/T	0.0618563	0.164627	intron-variant	RNF213	GRCh38.p7	17:80322285	CCCACTTTAGCCTCC[C/T]GAGTAGCAGGGACTA	57674
rs114830747	snp	C/T	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80274264	GGCTCCCTCTGGCCT[C/T]GAACAGCCTCTTAGG	57674
rs114842110	snp	A/T	0.0185938	0.0946107	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387038	GCAGCTCCCGAGGCC[A/T]CCACGCCACCTGTAT	57674
rs114865409	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391214	ATTTCCCCATTTACC[A/G]TGAGGCTGAACATGT	57674
rs114868020	snp	C/T	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80349681	CCGCGCTGAACATCG[C/T]AGGTTTCTAGGATCT	57674
rs114898084	snp	C/T	0.0154538	0.0865337	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372129	GTTTCAAAGACGCGG[C/T]TTCTGCCTTCAGCAA	57674
rs114903270	snp	C/T	0.0228947	0.104514	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365788	CTCCAAGTCTCATCA[C/T]GTCTCGGCGCTCTGG	57674
rs114905823	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80326437	AGTGTGGTGCTTTTG[C/T]TACAGCTGAGAAGCC	57674
rs114950817	snp	C/T	0.0495547	0.149404	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355841	AAGAAGCGGGGTGAA[C/T]GGGAATGGGGACTTA	57674
rs114971648	snp	A/G	0.0126979	0.078662	intron-variant	RNF213	GRCh38.p7	17:80280151	TGGGAAATGCAGGCA[A/G]CGTCCACACGGGGCT	57674
rs114983835	snp	C/T	0.0603597	0.1629	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320165	GAAACCCGGCCCCTT[C/T]AGCCATCATCCTCCT	57674
rs115005882	snp	C/T	0.0562307	0.157967	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260116	GCGGACCGCCGTGGC[C/T]CCTCCATCATCAGTG	57674
rs115036942	snp	C/T	0.0988009	0.199095	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356335	CCTGACTCCACTCCC[C/T]GGGACCAGCCCTGAG	57674
rs115044689	snp	C/T	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359061	CCCCACAATCTGTGC[C/T]CCTTACCCCTGGGAT	57674
rs115047000	snp	A/G	0.0785177	0.181917	intron-variant	RNF213	GRCh38.p7	17:80338676	TAATTTAAAAAAATT[A/G]AAACAGTCCAGGCAT	57674
rs115067038	snp	C/T	0.00519028	0.0506774	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360130	GAACGCTTCCAACAA[C/T]GTCCCTTTCAGCTGG	57674
rs115072215	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80318249	AAAAGACATTACTCC[A/G]AAAGAACCAGTGGGG	57674
rs115076865	snp	C/T	0.0275645	0.114116	intron-variant	RNF213	GRCh38.p7	17:80264934	CCCTTCCCCAGAGGG[C/T]GGCCTGGCTCCCTCC	57674
rs115135971	snp	C/T	0.000922448	0.0214563	synonymous-codon	RNF213	GRCh38.p7	17:80347704	GTACTACGTCCACCT[C/T]GGCGGCCAGAAGTAC	57674
rs115171660	snp	A/G	0.0115144	0.0749975	intron-variant	RNF213	GRCh38.p7	17:80272424	GCAGAGTAGGCCGAC[A/G]GGGATGCTGACAGCT	57674
rs115173377	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80337148	CCTAAACTTCTCTTA[C/T]TGTACTTGGGGACCA	57674
rs115187898	snp	A/C	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376106	AGAATAGAATATCAA[A/C]ATTAATGCTTACGTA	57674
rs115237033	snp	C/T	0.000891943	0.0210992	synonymous-codon	RNF213	GRCh38.p7	17:80348076	GACGGAGGAACTTCA[C/T]CAGAAGGTGTCTGAG	57674
rs115246536	snp	C/T	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359885	GCATAAGACAGTTCC[C/T]TAGTTCTGTCATAAC	57674
rs115266045	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80348541	CAAATAAAGTACCAC[A/G]TCCCAGGACTGGGCC	57674
rs115304377	snp	A/G	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80279858	ACACATGTAATGAAA[A/G]GACTTTTGCTTTTGG	57674
rs115320015	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396459	GCTCAGGGCCAAGTA[A/G]GTAAAGCCACCCAAG	57674
rs115385914	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358568	GTGCTGGGTGAAACG[C/G]AGCCCTCAACTTCAG	57674
rs115389637	snp	A/G	0.0168055	0.0901129	intron-variant	RNF213	GRCh38.p7	17:80337507	CAGCGAGGCAGAGGC[A/G]GGAGGCCGACCACAG	57674
rs115488230	snp	C/T	0.00755907	0.0610114	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354868	ATTTACCGACATTCA[C/T]GTTGATAACCCTAGA	57674
rs115501649	snp	A/G	0.021128	0.100586	intron-variant	RNF213	GRCh38.p7	17:80338044	TGGTGGTGTCATCTC[A/G]TCCGTGAGGGCTGTG	57674
rs115512083	snp	G/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80286372	AAATCGGAATTTCTG[G/T]CCCTGGTTCTGGCAG	57674
rs115516184	snp	A/G	0.0607341	0.163335	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387924	ACGGTACCACCCGCA[A/G]CTGGGCCAGGAACTG	57674
rs115529540	snp	C/G	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365280	GTTTACTAAAAGGAG[C/G]CCAGCATGGATGCTG	57674
rs115533362	snp	A/T	0.0494327	0.149241	intron-variant	RNF213	GRCh38.p7	17:80284780	CAGTGGCTTCCCCTG[A/T]GATCCACCTGCTACT	57674
rs115592242	snp	C/G	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379072	GCGTGCATGCGTGTG[C/G]TCCCAGCTACTTGGG	57674
rs115604492	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80284081	TATGAAAATTACGGC[C/T]GGGCACAGTAGCTCA	57674
rs115614008	snp	A/G	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80277197	CCTTTGATATGAAAT[A/G]TCCACGATAGACTCA	57674
rs115641751	snp	C/T	0.0123036	0.0774623	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362989	GGACAGAATAGCACA[C/T]ATGGTTTCTAATTTC	57674
rs115670109	snp	A/G	0.0648419	0.167978	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397506	CTATAGATTACAGAC[A/G]TTATATAGAAAAGCA	57674
rs115709455	snp	A/C	0.0640965	0.167152	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352745	AAGCTGTCGATGGGC[A/C]TAGAATCGGGTCGTG	57674
rs115759653	snp	A/C	0.0626037	0.165477	intron-variant	RNF213	GRCh38.p7	17:80339107	GCCTGTGGACAGGGC[A/C]GTCTTTTGGCGGTAG	57674
rs115775716	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80311808	TGACACTTGCACGAT[A/G]TGCGGGGCTGTGCTT	57674
rs115784982	snp	A/G	0.0236746	0.106192	intron-variant	RNF213	GRCh38.p7	17:80263899	GGGCCGAGGTCCTCT[A/G]TGGCTACTGAGGCTC	57674
rs115808000	snp	A/G	0.00599301	0.0544113	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360198	CTCAGTACATCACAG[A/G]CGCAGAAGGTGAGGC	57674
rs115824037	snp	A/G	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80274912	GTTGGGGGTGTGTGA[A/G]TGGGGTGTGAGTGGG	57674
rs115828600	snp	C/T	0.0168055	0.0901129	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382368	AAATCACAATGACCA[C/T]TGTGAGGACAATGTT	57674
rs115838702	snp	A/C	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357254	CAAGAATTTTGAAAT[A/C]GAGCTATTATTGTTA	57674
rs115863856	snp	A/G	0.0185938	0.0946107	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357903	TGAGGTGGGAGGATC[A/G]TTTGAGCCCAGGTAT	57674
rs115867721	snp	A/G	0.00248488	0.0351606	missense	RNF213	GRCh38.p7	17:80347351	GCCAATTTGCCCGAG[A/G]CCAAGTGCTCAGAGG	57674
rs115969944	snp	C/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80332769	CCTGTGTGTGTGGTA[C/G]TTGAGGCCTGAATAT	57674
rs115976016	snp	A/C	0.0248432	0.108648	intron-variant	RNF213	GRCh38.p7	17:80283336	AGGTGTCAGCCCTGC[A/C]GGTGTGATGATGTCA	57674
rs115983589	snp	C/T	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80305531	AGAACAGGGCTACCC[C/T]ATAGGAGCATGCCCA	57674
rs116000835	snp	C/G	0.0158469	0.0875917	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362264	CATACTTTTGACTAC[C/G]TAAAAATTTTAAACT	57674
rs116003223	snp	C/T	0.108048	0.20579	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359023	CAGCATGGCGTGACA[C/T]GGAGACAGTGCGCTG	57674
rs116007874	snp	A/G	0.00912758	0.0669364	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354437	TGTTTCTGCCTTTGT[A/G]CAGCCTCTTTCTTGC	57674
rs116010947	snp	A/G	0.0287284	0.116357	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287232	TGGGAATGGTGGTTC[A/G]CGCCTGTAATCCCAG	57674
rs116036366	snp	A/G	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80304171	GGCCTTTAGTATGCA[A/G]TGAACCTTTATTGAT	57674
rs116122447	snp	A/G	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80276730	GCCGTTAAGGAAGCA[A/G]CAAGGCAGTTGATCC	57674
rs116130179	snp	G/T	0.120674	0.21395	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368848	GGCTCTCTGGACTCA[G/T]CAGGCCTCAGCCCGG	57674
rs116144111	snp	A/G	0.0185938	0.0946107	intron-variant	RNF213	GRCh38.p7	17:80274171	GGGCTTTGAAGCTTT[A/G]GGTGTGGGGTGGGTG	57674
rs116163077	snp	C/T	0.0337553	0.125452	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396067	TGGTGGTGATTTACC[C/T]GAAAATCTTCACAAC	57674
rs116211382	snp	C/T	0.0267878	0.112589	intron-variant	RNF213	GRCh38.p7	17:80335656	GAAATTGCTCAGGAA[C/T]GGCAAGATATCGTTT	57674
rs116306771	snp	C/T	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362761	CTTTGCTTCGAAAAA[C/T]AAGAAATAGTTTAAT	57674
rs116308209	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359057	ACAGCCCCACAATCT[A/G]TGCTCCTTACCCCTG	57674
rs116309052	snp	C/T	0.00438332	0.0466095	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321509	TGTCTTCATTTCTCC[C/T]GGGTGTATACCTCGA	57674
rs116366411	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389674	AACTGGTAGATAGGA[C/T]AGAGATGGCCTTCAC	57674
rs116370936	snp	A/G	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80304301	TATTTAAGGGCCTTC[A/G]CTGAGCCCACTTGGG	57674
rs116425227	snp	C/T	0.0146672	0.084371	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352876	TGTGCAATGTCCCTG[C/T]TTAGGGCTGAGCAGC	57674
rs116453346	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80350997	TTGGATATTTTTATA[C/G]TGTTTGTAGGGGAAG	57674
rs116464658	snp	A/C	0.00535745	0.0514784	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376584	GCCTTCACTGGAACA[A/C]CCCCCAGAGCTTGTC	57674
rs116468411	snp	A/G	0.000116444	0.00762946	synonymous-codon	RNF213	GRCh38.p7	17:80346768	CTTCCAGTGCAGCCC[A/G]CACTCCACCCCACAG	57674
rs116469618	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80281590	CACCACTCACACACT[C/G]CCAACACACACAGCC	57674
rs116516842	snp	C/T	0.00148854	0.0272406	intron-variant	RNF213	GRCh38.p7	17:80336498	TGTACACAGCCGTTT[C/T]CAATGATATTTAAAA	57674
rs116536300	snp	C/T	0.0170251	0.090679	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395514	ATGACAGCATCCTGG[C/T]GACTCCACAGTGGAG	57674
rs116548241	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80312653	CTAAGGAACAGGCCC[A/G]GGAGTCTGCAGGGCC	57674
rs116554076	snp	A/G	0.077417	0.180873	intron-variant	RNF213	GRCh38.p7	17:80343540	TAACCTAGACGTAGA[A/G]CCCACTGCACACACA	57674
rs116554595	snp	A/G	0.0170251	0.090679	intron-variant	RNF213	GRCh38.p7	17:80304142	CCTAAAGATCCAATC[A/G]TTCAGGTAAAAGTGG	57674
rs116594105	snp	A/G	0.00343724	0.0413135	missense	RNF213	GRCh38.p7	17:80346166	AGCCTAGATGAAAAC[A/G]GGACTCGCGTGATCA	57674
rs116608867	snp	C/T	0.00142848	0.0266871	missense	RNF213	GRCh38.p7	17:80340314	GCCGTGTTCAATGAC[C/T]GGCTGTGTGTTGGGA	57674
rs116623471	snp	G/T	0.0240643	0.107019	intron-variant	RNF213	GRCh38.p7	17:80318109	AGCCATCCCTCTGAA[G/T]TCAAGTCACCTGTTT	57674
rs116626383	snp	C/G	0.084728	0.187577	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320965	GCACTTCAACCTGGG[C/G]GACAGAGCAAGACCC	57674
rs116639116	snp	C/T	0.030278	0.119257	intron-variant	RNF213	GRCh38.p7	17:80293940	CTGCTGGGCCCAGGG[C/T]GCAGAGCTGGGGTGG	57674
rs116655373	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270470	CCACTCACTGGCCGC[A/G]TCTCTGTGCTCCCTG	57674
rs116672724	snp	C/T	0.0126979	0.078662	intron-variant	RNF213	GRCh38.p7	17:80291885	CAGGTGCCAATCCCG[C/T]GGTACTGGACGCGTC	57674
rs116673179	snp	A/C	0.122411	0.214991	intron-variant	RNF213	GRCh38.p7	17:80274088	GCTTCGGGGCAGGGA[A/C]CTGAGCGTCCGCTGG	57674
rs116677277	snp	A/G	0.00484977	0.0490037	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353531	CTTGGAACACCGGGC[A/G]GAAGACGGCCATGAG	57674
rs116693616	snp	C/T	0.00989926	0.0696537	intron-variant	RNF213	GRCh38.p7	17:80343344	AGTGCCCTCCAGCGT[C/T]AGCCGATGGCCACAT	57674
rs116694967	snp	C/G	0.00591307	0.0540516	missense	RNF213	GRCh38.p7	17:80336256	TGCTTCCATGACGCT[C/G]TGCAGGGCTACGCAT	57674
rs116708858	snp	A/G	0.02016	0.0983543	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364308	ACATAGGGCTTGCTT[A/G]TAATCCCAGCCGCTG	57674
rs116722283	snp	A/G	0.0205877	0.0993479	missense	RNF213	GRCh38.p7	17:80332189	ACAGCCACATCTTCC[A/G]GCTCTTCTGGCGGGA	57674
rs116750502	snp	G/T	0.0146672	0.084371	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360734	GATGCCAGAAGATTT[G/T]CCCTAGTCCAGAAAA	57674
rs116760165	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397915	CATGGATCCTGAGAG[C/T]GCTCTCAGGCAGGCA	57674
rs116842651	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355039	TTTCTGTCACCCATG[A/G]GACTAACCTTGATTA	57674
rs116875444	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80317457	CCTAGAAGAGCGCTT[C/T]GGAGTCTTACTGAGA	57674
rs116898047	snp	C/T	0.0267878	0.112589	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353899	CGTCTCTTCTTTGTC[C/T]GTGAGGACCGCCGCC	57674
rs116898060	snp	A/G	0.0535932	0.154675	intron-variant	RNF213	GRCh38.p7	17:80328732	GAGCTGCTGACGCCC[A/G]CTGCAGAAGATGAGG	57674
rs116926142	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80308959	AGTCATCAATGGTAA[C/T]CATTTTCTGGCTTCT	57674
rs116946917	snp	A/G	0.0535932	0.154675	intron-variant	RNF213	GRCh38.p7	17:80350079	ATCATCTTCTGCAAC[A/G]CGGTGTCTGGCCTAA	57674
rs116948489	snp	A/G	0.0942659	0.195673	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373030	GCAGTTCTGTATCCG[A/G]GTGGAGAACGACTGG	57674
rs116952508	snp	A/G	0.17654	0.238964	intron-variant	RNF213	GRCh38.p7	17:80318741	ACCGCGCCCAGCTAT[A/G]TTTTTGTATTTTTTG	57674
rs116956704	snp	C/T	0.0103295	0.0711199	intron-variant	RNF213	GRCh38.p7	17:80326374	AGAGTTGTCATCTAT[C/T]TCTGCCACCATCACA	57674
rs117015282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309635	AACAAAGGCCATAGC[A/G]CCACACATCTGCCCC	57674
rs117034436	snp	A/G	0.0456336	0.143994	intron-variant	RNF213	GRCh38.p7	17:80286048	CCAGATCTCAGTGAG[A/G]CCCTGTTTTAGAGTC	57674
rs117053144	snp	C/T	0.11963	0.213316	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355810	CGGGGTGACCGGGAA[C/T]GGGGGCTTACAGGAG	57674
rs117081212	snp	C/G/T	0.124444	0.216185	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355414	GGGAATGGGGGCTCA[C/G/T]GGAGGAAGAAGCGGG	57674
rs117088701	snp	C/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80297845	CACCTGTAATTCCAG[C/T]ACTGGAGAGGCTGAG	57674
rs117109192	snp	C/T	0.02016	0.0983543	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393140	TACACCACCACGTGC[C/T]CAGCTAATTTTTGTA	57674
rs117159774	snp	A/G	0.000445541	0.0149188	synonymous-codon	RNF213	GRCh38.p7	17:80347869	TCTGGATATCAACAC[A/G]GTGCTGGAGAAATGG	57674
rs117163366	snp	C/T	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365452	GTCTTGTCCCTTCAT[C/T]GTCCCTAATGTTCAG	57674
rs117214360	snp	C/T	0.143622	0.226238	intron-variant	RNF213	GRCh38.p7	17:80290332	GCGTTCACGTGTGTG[C/T]GCGCACGTGTGTGCG	57674
rs117219789	snp	A/G	0.0185938	0.0946107	intron-variant	RNF213	GRCh38.p7	17:80300536	GGCATGAGCCACCAC[A/G]CCTGGCCTCATTGTG	57674
rs117221106	snp	C/T	0.0228947	0.104514	intron-variant	RNF213	GRCh38.p7	17:80290390	GCGTGCACGTGTGTG[C/T]GTGTACGTGTGCTTG	57674
rs117227113	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371477	ATTCATGTTTTGGAA[A/G]ATATTTTAAATGTTA	57674
rs117254855	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359024	AGCATGGCGTGACAC[A/G]GAGACAGTGCGCTGC	57674
rs117302980	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80265827	ACAACCCCAGCATGT[C/T]TGCAGGCCAAGGTGG	57674
rs117308931	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80289923	CTCTCAGGGGATATC[C/T]AGGCTGCCCTTCTAG	57674
rs117335306	snp	A/C	0.0707826	0.174302	intron-variant	RNF213	GRCh38.p7	17:80297001	ACAAATAAAAAACAA[A/C]CAAATAAACGCCGCA	57674
rs117337485	snp	C/T	0.0162398	0.0886349	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363936	TCACTCCGCATTTGC[C/T]GAACCCTTAGTGAGT	57674
rs117343525	snp	C/T	0.0165278	0.0893908	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259193	GTCACCTTGGCTGGG[C/T]GCAGTGGCTCATGCC	57674
rs117380076	snp	A/G	0.152778	0.230321	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355728	GGAAGAAGCGGGGTG[A/G]ACGGGAATGGGGGCT	57674
rs117435714	snp	C/T	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80292710	TGTCTGCAAACTTGA[C/T]AGACAGAGATCAAGA	57674
rs117439438	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328249	GTGGCGGGGAAGGTG[C/T]GGCGCTTTCAAAGCA	57674
rs117459315	snp	C/T	0.132751	0.2208	intron-variant	RNF213	GRCh38.p7	17:80300190	GCATTCCTTTTTCTC[C/T]GCAACCTCACCAGCA	57674
rs117490352	snp	A/G	0.0165278	0.0893908	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351330	CGCTTAAGAGAAAAG[A/G]AGGAATGGAAAGTTC	57674
rs117505420	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80276755	TGATCCAAAAGTTAC[G/T]CATAAAATTATCCTA	57674
rs117505771	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80341719	CTCCAGCCTAGGCAA[C/T]GGGGCAAGGCCTTGG	57674
rs117526444	snp	G/T	0.10237	0.201756	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397633	CTCACGCAGACCCCT[G/T]AAGAGTTGTGAGCCC	57674
rs117544462	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318142	AGTGAAGCTACTTCT[C/G]TCTCACTACCAAGTC	57674
rs117560597	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80336763	TTTAAAATTAGCCAG[A/G]CATGGTGGTGTGCGC	57674
rs117589727	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387059	CCACCTGTATCTCCG[A/G]GCCGCAGGGCTCTCC	57674
rs117627863	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80317374	CTCAGCAGTGCCTCT[A/C]TGTGGGCAGGGATGG	57674
rs117669586	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80281578	ACGCCCCACTCACAC[C/G]ACTCACACACTGCCA	57674
rs117692007	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393563	CTCCTCGTCTGCGGC[A/G]TGGACTTGATCATGG	57674
rs117705614	snp	A/C/T	0.00605258	0.0546791	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364529	ACAGGGGCTGGTGAC[A/C/T]GAGCACGTCTTCTTA	57674
rs117729174	snp	C/T	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80296001	ATTTTTATTATATTC[C/T]GTCCTCTGTTGAATT	57674
rs117752548	snp	A/G	0.0165278	0.0893908	intron-variant	RNF213	GRCh38.p7	17:80262040	TGGAGGATTTTTCGA[A/G]TTTTCTGGTCTGTGG	57674
rs117760765	snp	A/G	0.18	0.24	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355486	GGAATGGGGGCTCAC[A/G]GAGGAAGAAGCGGGG	57674
rs117781188	snp	A/T	0.0193772	0.0965046	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352304	CCATGAAAACATGAA[A/T]CCTGGGATGGGAGGC	57674
rs117794958	snp	A/T	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375608	CTACTCGGGAGGCTG[A/T]GTTAGAATCGCTTGA	57674
rs117796339	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315631	TGGTCCGTGGAGGTG[A/G]TGGTGGTGGTGGTAA	57674
rs117844399	snp	A/G	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321033	TTGTAGCTTGTGTCC[A/G]TTTACGTTAAGTATT	57674
rs117847664	snp	G/T	0.0479149	0.147179	intron-variant	RNF213	GRCh38.p7	17:80304135	CATTGTTCCTAAAGA[G/T]CCAATCGTTCAGGTA	57674
rs117857085	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80337014	GGCCAGCCTCCGGAC[A/G]GCTGCTCTGCATGTG	57674
rs117893374	snp	A/G/T	0.00716521	0.0594565	intron-variant	RNF213	GRCh38.p7	17:80305542	ACCCCATAGGAGCAT[A/G/T]CCCAGAATGGCCAGC	57674
rs117911468	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365587	CACCAGCTCGTGTCT[C/T]GTGGTCCTAAACTTA	57674
rs117920635	snp	C/G/T	0.186804	0.250725	intron-variant	RNF213	GRCh38.p7	17:80274602	TGGGGGGTGAGTGGG[C/G/T]TGAGTGTGGGGGGTG	57674
rs117929479	snp	A/T	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382244	CTTTCTATTTTAAAA[A/T]TTTAAATCCATACAG	57674
rs117945446	snp	C/T	0.0162398	0.0886349	intron-variant	RNF213	GRCh38.p7	17:80299305	TGTGCAGTTTCGTTT[C/T]TTCAGCGTGCTTTCA	57674
rs117953456	snp	A/G	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80267778	TCTCCAGATCTGGCT[A/G]AGGTTATTGATGGAG	57674
rs117980117	snp	C/G	0.0236746	0.106192	intron-variant	RNF213	GRCh38.p7	17:80300372	TCGGCACAAGCGATT[C/G]TGCTGGGATTGGTAG	57674
rs117982582	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388507	GGATACACAGGGCAG[C/T]GCGGCACTACGCTGC	57674
rs118033223	snp	A/G	0.0422008	0.138995	intron-variant	RNF213	GRCh38.p7	17:80303733	CACACATCACATGTG[A/G]CTAATTTTTGTATTT	57674
rs118033730	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80265975	AGTTGGGATGGGGAC[A/C]TGGGAAGCCCATGGC	57674
rs118040689	snp	A/G	0.0150606	0.0854603	intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360408	GTGAGAGGCCCCGGC[A/G]GGACCAGAAACCTTT	57674
rs118050447	snp	A/G	0.127944	0.218179	intron-variant	RNF213	GRCh38.p7	17:80279751	TGGGATTACAGACGT[A/G]AGCCACTGTGCCTGC	57674
rs118097770	snp	C/T	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80328570	AGCAGATCTTTATTT[C/T]GGAGAGAAGGCTTTA	57674
rs118122982	snp	A/G	0.0138799	0.0821421	intron-variant	RNF213	GRCh38.p7	17:80277134	CCTGGATGGACCCCA[A/G]AAACATGCTAAATGA	57674
rs118128489	snp	A/G	0.00352239	0.0418185	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319396	GGCTATGAAGCACCC[A/G]CTGGGTCTCAGCTCC	57674
rs118129095	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365825	CACAGGGCTTTCAGC[C/T]AGGTCCAGCGTGGGT	57674
rs118151456	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357711	GTGCGGTGGCTCACA[C/T]CTGTAATCCCAATAC	57674
rs118153619	snp	C/T	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392256	ATATACATTTATGTT[C/T]TTTCAACTTTTTCAA	57674
rs118155465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265512	TTTTGAACATTTATC[A/G]AAAACCAAGAAATAC	57674
rs118162898	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80341731	CAACGGGGCAAGGCC[C/T]TGGTCTTTTAAAAAA	57674
rs118178130	snp	A/G	0.0209421	0.100162	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370024	ACTTGTACTGGTTGT[A/G]TATTCTGACATTTTC	57674
rs137891482	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80337579	TTCTCTCCTTTTGTC[C/T]CCATAGTGTGACTCC	57674
rs137910853	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365568	CCCGGACACGCACAC[A/G]CCACACCAGCTCGTG	57674
rs137915874	in-del	-/AC	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80269253	ACAACACCCTCACAG[-/AC]ACAACCAGAACAATA	57674
rs137918227	snp	C/T	8.23621e-05	0.00641672	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376326	CTGTGAGCAAATTCA[C/T]TGGCGAATGCAAGAT	57674
rs137919301	snp	C/T	8.5563e-05	0.0065402	missense	RNF213	GRCh38.p7	17:80340294	AGCAGACCCTGTCGG[C/T]GGCAGCCGTGTTCAA	57674
rs138004000	snp	C/T	5.0358e-05	0.00501761	missense	RNF213	GRCh38.p7	17:80347157	CCAAAGCCTACGAAA[C/T]GGTGTGTAAGCGCCA	57674
rs138009036	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80266795	GTGTGAGCCACCCAC[C/T]GCACCTGGCCTCATG	57674
rs138011023	snp	G/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80294503	TTACTGTGGGACGTC[G/T]AGGATGTCTGTTTGC	57674
rs138029774	snp	A/C	0.0121924	0.0771203	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372731	GAGCCTGAGGGAGGC[A/C]CAGGCAAGTCTTCTC	57674
rs138032722	snp	C/T	0.000543545	0.0164766	synonymous-codon	RNF213	GRCh38.p7	17:80345691	GCTGGTCAAGGTGCA[C/T]GGAGGAACAACTGCA	57674
rs138036703	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283394	GAGGTTCTGGGATGG[C/T]GGCTTGAGGGCAGTG	57674
rs138044665	snp	A/G	0.00200773	0.0316202	missense	RNF213	GRCh38.p7	17:80345314	CTGCAGCCCAACATC[A/G]ACGGCAGTGTCGATG	57674
rs138048764	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291574	CGTTTGAGAATAACT[A/T]AAATTTCCGGGGTAG	57674
rs138066284	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362666	TTGAGCACCTTATCC[A/G]ATCTGAACTGCTGAC	57674
rs138069704	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265893	TGGGCAATGTAGAAA[A/G]ACTCCATCTCTGTAT	57674
rs138073471	snp	A/G	6.59435e-05	0.00574172	missense	RNF213	GRCh38.p7	17:80347775	TTCACCCCAACTTCC[A/G]CCTGATTGTCATTGA	57674
rs138083033	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312645	TCCTGTGTCTAAGGA[A/G]CAGGCCCGGGAGTCT	57674
rs138105446	snp	A/G	0.0166325	0.0896639	intron-variant	RNF213	GRCh38.p7	17:80262402	TTATGGCATTGGGAC[A/G]GGGGCTTGGGGCTGG	57674
rs138110704	snp	A/G	1.64819e-05	0.00287066	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386367	CCGCTCTCGTCAGCT[A/G]CTTGATTCGCCTACA	57674
rs138114099	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397360	CCACATATTGTCTTA[C/T]GCCCAATTTCTGCCT	57674
rs138130613	snp	C/T	0.000527001	0.0162241	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389234	AGTCCTACAGCGATG[C/T]CTGTGAAGTGCTGTC	57674
rs138136667	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80334450	GAGTTCACACCGGTA[C/T]AGTATTTCCCATGTG	57674
rs138150644	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341609	CAGGCATGGTGGTGC[A/G]TGCCTGTGATCCCAG	57674
rs138164707	snp	A/G	0.00815108	0.0633175	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386481	CAGCCCAGAGTCCCT[A/G]AGCCCAGTGGGGCAG	57674
rs138164993	snp	A/T	0.00045854	0.0151347	intron-variant	RNF213	GRCh38.p7	17:80331961	AAATAAAATGGAATC[A/T]TGATTAGAGCTTTGA	57674
rs138186259	snp	A/G	0.0869089	0.189476	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358725	ACCGTCCTGGCCAAC[A/G]TGGTGAAACCCCGTC	57674
rs138196543	snp	A/G	0.00104763	0.0228631	synonymous-codon	RNF213	GRCh38.p7	17:80295562	CCACCATCAGGTGAA[A/G]AGATACCTGTGGCAA	57674
rs138210678	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80347896	ATGGCAGAAGAGCAT[C/T]GTGGAGGAGCTCTGT	57674
rs138216615	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80299825	CGGTATTTGGTTCTC[A/G]TTCCTGAGTTAATTT	57674
rs138223459	snp	A/G	3.3151e-05	0.00407117	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381667	GCCGACGAGACCATC[A/G]GCGTGGTCCACCTCG	57674
rs138228755	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352753	GATGGGCATAGAATC[A/G]GGTCGTGTATAGTAT	57674
rs138228835	snp	C/G	0.000329413	0.0128296	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385126	CAGAACGTCCAGCAA[C/G]TTGAATACAGCTCCA	57674
rs138270447	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382706	CTCTTACTATTGAGC[C/T]CAAGTTCTGTTCTTT	57674
rs138278085	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360178	GGAGGAGCTGTGGGT[C/T]CAGGCTCAGTACATC	57674
rs138285125	snp	C/T	0.000307953	0.0124049	missense	RNF213	GRCh38.p7	17:80347261	AATAGAAAGCCTTCC[C/T]CGCAAGACATTGCAC	57674
rs138341287	snp	C/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319582	GTGTGGCACAAGTCA[C/G]ACGGGCTTGCAGGCC	57674
rs138353197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376119	AAAATTAATGCTTAC[A/G]TATGTGGATGCTGTG	57674
rs138385915	snp	C/T	0.000153988	0.00877328	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319417	TCTCAGCTCCTCCGC[C/T]AACTCAGAGATTGGG	57674
rs138386129	snp	A/G	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80263332	CCGTGGGACCCTGCC[A/G]AACAGCACGTGGCTG	57674
rs138389700	snp	C/T	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80310133	CCCCATGTCTCTGAG[C/T]TCTGTCTGTGTGGTG	57674
rs138418700	snp	G/T	0.000131841	0.00811808	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393414	TGAAATGGCATCTCA[G/T]TTCCCAGAAGAGATA	57674
rs138420410	snp	C/T	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80342046	TTGAGTGATCACCCG[C/T]CTCAGCCTCCCAAAG	57674
rs138421996	snp	A/G	0.000559956	0.0167232	missense	RNF213	GRCh38.p7	17:80307149	CAGGATGTTCAGAAC[A/G]TTCAGAACATTTTAG	57674
rs138422793	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277369	TTGGGAGGCTGAGGC[A/G]GGTGGATCACTTGAG	57674
rs138449130	snp	A/G/T	0.00159617	0.0282053	intron-variant, missense, stop-gained	RNF213	GRCh38.p7	17:80288913	CATTCCAGCGGAGAG[A/G/T]GAGTCAGGAAACCGA	57674
rs138461014	snp	C/T	0.000313198	0.01251	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319393	AAGGGCTATGAAGCA[C/T]CCGCTGGGTCTCAGC	57674
rs138478778	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80274232	CTTCTTGGAAGGGTA[C/T]GGCTGAGCCACCTTT	57674
rs138493748	snp	A/G	0.000280267	0.0118345	missense	RNF213	GRCh38.p7	17:80347814	ACGTCGTGTACAAAC[A/G]CTTTCCCATCCCCCT	57674
rs138495473	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302695	CCCAGTTTCTACAAA[A/C]AAACAAACAAAAAAA	57674
rs138516230	snp	A/C/T	0.000922372	0.0214559	missense, synonymous-codon	RNF213	GRCh38.p7	17:80345997	GGAGGAGACGGCCGA[A/C/T]AGGCTGGGCTCCATT	57674
rs138518812	snp	C/T	4.94205e-05	0.0049707	missense	RNF213	GRCh38.p7	17:80309040	GAGGAGGCCTTGTCA[C/T]CATCCTACCTGACTG	57674
rs138525780	snp	C/T	8.34286e-05	0.00645812	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372637	GGGCCGAGAGCCTGC[C/T]AACGAGGCCTCGGTT	57674
rs138535898	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363085	AAATATATTCTAAAA[C/G]CTTTTTTGAATCCCA	57674
rs138538903	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80312779	CACACAGATGCCGTT[C/T]CCTCCCTCCCTCTTT	57674
rs138541507	in-del	-/GAGGTAGAGGACAGGCCGTTTTCCTTAA	0.216649	0.247765	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365516	GGACAGAAAGCAGGG[-/GAGGTAGAGGACAGGCCGTTTTCCTTAA]GAGCCCAATCCCGGA	57674
rs138555300	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397843	AGGCAGCCCCTCAGA[C/T]GGCTTAGGCCTGCCC	57674
rs138580485	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383131	GGAAGGGTCCCGGCG[G/T]CTGCTGAATGCTCCT	57674
rs138587836	snp	A/G	0.000411743	0.0143423	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376375	CAGCCGTTTTGCAAC[A/G]TCGCTCGTGGACAAT	57674
rs138588912	snp	A/G	0.0244538	0.107838	intron-variant	RNF213	GRCh38.p7	17:80310314	CTGGAGTGTAGTGGC[A/G]CCATCTCAGCTCACT	57674
rs138595111	snp	A/G	0.00471676	0.0483336	missense	RNF213	GRCh38.p7	17:80344886	ACCTAGACACGTTTC[A/G]GTATCAAGAAGGCTC	57674
rs138615753	snp	A/G	8.24559e-05	0.00642037	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367760	CAGTGTCTTCGAGAG[A/G]ACTCTGACGTGAAGA	57674
rs138618978	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392080	GCCTGTCCTCTCTCT[C/T]CTTGTGCTTTCACAT	57674
rs138629029	snp	A/G	5.14831e-05	0.00507335	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288313	GGCAGCTCTGAGCCC[A/G]GGACAGAACTGCAGA	57674
rs138640049	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80337194	GACTTGGGACTCCAC[A/G]GCCATTGCTTCCAGC	57674
rs138677961	snp	A/C	0.000729413	0.0190834	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288193	ATCCCCTCTGGGGGC[A/C]GAGGCCTGTCCCAGG	57674
rs138689611	snp	A/G	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80277783	AGTGTATGCGTGAAC[A/G]GTGCTCTAAGCGCAG	57674
rs138709512	snp	A/G	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80272065	CAAGACGGGTGGATC[A/G]TGAGGTCAGGAGTTC	57674
rs138713917	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80284202	TCTGTACAAAAATAC[-/A]AAAAAAAAAAAAATT	57674
rs138724571	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80306937	TTGGTGGAGAAAATG[G/T]TATAAGTTTAAATCC	57674
rs138758274	snp	C/T	0.046775	0.145601	intron-variant	RNF213	GRCh38.p7	17:80285927	GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	57674
rs138759764	snp	A/C/G	0.00239393	0.0345281	intron-variant	RNF213	GRCh38.p7	17:80316885	TCTTGCGACCTTTTT[A/C/G]AAAGTTCAAAAATTT	57674
rs138770190	snp	A/G	8.2494e-05	0.00642185	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352976	TCGATGACCTCCGGA[A/G]ATCCACCCTCATGGT	57674
rs138774784	snp	A/G	0.0130921	0.0798413	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365245	CAGCGCTGGCTGTCC[A/G]ACCTTTGGAGCACAG	57674
rs138778980	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80314967	GTGATGGTGGTCGTG[G/T]AGGTGATGGTGGAGG	57674
rs138790004	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280567	CAAGCAATCCTCGTG[C/G]CTCAGCCTCCCGAGT	57674
rs138803237	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379293	AAGTGCCACAGGCTA[C/G]TGTGATAGATGGAGG	57674
rs138806831	snp	A/G	1.66084e-05	0.00288165	missense	RNF213	GRCh38.p7	17:80347054	CGTGGCAGCCCCAAC[A/G]AGACAGAGCTCATAG	57674
rs138811474	snp	C/G	4.94238e-05	0.00497086	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390071	CCCGGAAAATGCTAA[C/G]CTCCTCAGCACATTC	57674
rs138825989	snp	C/T	0.000342212	0.0130763	missense	RNF213	GRCh38.p7	17:80325127	CCTGGCCTAGGACCG[C/T]GGACAACTTCAATGA	57674
rs138841786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359430	TCTAGAAGCTGAGGC[A/G]GGAGGATTGCTTGAG	57674
rs138842793	snp	A/G	3.29891e-05	0.00406122	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386709	TCCGTGGATGCCGCC[A/G]AGGTCACTGAACTGC	57674
rs138848873	in-del	-/T	0.124324	0.216115	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392997	TGTTATATGGGAGCC[-/T]TTTTTTTTGAGACAG	57674
rs138876971	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80274099	GGGACCTGAGCGTCC[A/G]CTGGGTGCGTGTCTT	57674
rs138880468	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356394	CCACTCTGCTGTTCA[C/T]GCAGCACTAGGCCTG	57674
rs138979388	snp	A/G	1.65075e-05	0.00287289	missense	RNF213	GRCh38.p7	17:80348258	ACCTGCACACGGCAG[A/G]CCTGGAGCGCCACGC	57674
rs139013218	snp	A/C	0.0360663	0.129354	intron-variant	RNF213	GRCh38.p7	17:80299359	CCCATAACTTCATTG[A/C]GATAGATTCCTACAA	57674
rs139017008	snp	A/T	0.0182019	0.0936463	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356845	TCTGTACTATATATT[A/T]AAAAAATGTAGGTAT	57674
rs139033181	snp	A/C	0.0368353	0.130617	intron-variant	RNF213	GRCh38.p7	17:80296168	GGGACTACAGGTGCA[A/C]ACTACCACACATGGC	57674
rs139035227	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80327658	GGGGAAAGCAGAAGG[G/T]AGTGGAATGATTGGC	57674
rs139039955	snp	C/T	0.0295035	0.117819	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382100	GCTGGGAGCACGTGT[C/T]GTCCACACAGAGCGT	57674
rs139051119	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80308427	CTCCTGAGTCCCTCC[C/T]AAGGCTCCTCCTGAG	57674
rs139077549	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389724	GTACAGGGCAGAACG[A/G]AGAGAAGAATGCCTG	57674
rs139113160	snp	C/T	0.000629056	0.0177238	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353575	CGGAGGCCAGCACAT[C/T]AGGGGAGGTGGCAGA	57674
rs139117822	snp	C/T	0.0345262	0.126772	intron-variant	RNF213	GRCh38.p7	17:80282899	GATGGGGTTTCCCCA[C/T]GTTGGCCAGGCTGGT	57674
rs139157027	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335248	CAGAGAGATTTTTCT[C/T]ACTTCTCCATTGATG	57674
rs139168662	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331523	CCTCCTGAGTAGCTG[A/G]GATTACAGGTGCGCT	57674
rs139217743	snp	C/T	0.00241893	0.0346932	intron-variant	RNF213	GRCh38.p7	17:80278917	TGTGAGCAGGTAGTC[C/T]GAGTCAATAGTTTGG	57674
rs139220263	snp	A/G	3.30551e-05	0.00406528	synonymous-codon	RNF213	GRCh38.p7	17:80295691	TGTCCTTTTTGTAGT[A/G]GAAAAAATTGAGCTT	57674
rs139223481	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80350078	CATCATCTTCTGCAA[C/T]GCGGTGTCTGGCCTA	57674
rs139250788	snp	A/G	0.00123648	0.0248337	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363831	TGCTTCATCTGGCGC[A/G]CGCTCACCAGGAGCC	57674
rs139265462	snp	C/T	0.00108681	0.0232857	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368043	CACGTGCACTGCCTG[C/T]GCTGCCTCAGGGCCT	57674
rs139279361	snp	A/G	0.00900733	0.0665021	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376967	TCCACTGGTACAGTA[A/G]GTGTTGGGGTCTAGA	57674
rs139292810	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367598	CATTCAGAGTTCAAG[C/T]GTTAAACACAGGATC	57674
rs139300471	snp	C/T	1.64806e-05	0.00287054	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369523	CATTGAAAAGCATGC[C/T]CGCTTCCGGCAGATG	57674
rs139305565	snp	A/G	0.000346309	0.0131543	synonymous-codon	RNF213	GRCh38.p7	17:80313128	AAAGAACATGCTCAC[A/G]TCTTCAGGTGCCTCA	57674
rs139321428	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80325520	GATCAGGAAACAAAT[A/G]GAGAAGGCAATGCGA	57674
rs139349808	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335801	ACCAACATGGTGAAA[C/G]CTGGTCTCTACTAAA	57674
rs139368915	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80284462	GGCAGGAGAATGGCA[C/T]GAACCCGGGAAACAG	57674
rs139395656	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364154	TTCCCTAAAGGTGAG[G/T]TGGGACTTGACAGGC	57674
rs139428059	snp	C/T	0.00049518	0.0157272	missense	RNF213	GRCh38.p7	17:80348156	GGCTGAGCGCCTACT[C/T]GCTGGGCGGGTTCGC	57674
rs139431747	snp	A/G	6.59098e-05	0.00574026	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380876	CGTGCTGGGCAACCC[A/G]CAGCGGAGAGACGTG	57674
rs139435796	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326168	CTGTTGCGCAAGTTA[A/G]CATGTAGTAGAGTGA	57674
rs139438677	snp	C/G	1.68156e-05	0.00289957	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363608	CTGTCCGTCTCCCCA[C/G]ACCCTGGACGCATTT	57674
rs139450510	snp	A/G	0.000230753	0.0107389	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386929	CTGCTCATTTGGTGT[A/G]TCTGTTGTGAACAAG	57674
rs139456294	snp	C/T	0.00135517	0.0259952	missense	RNF213	GRCh38.p7	17:80298371	GCATGGACACAAGGA[C/T]GTACACCTGGCTGGG	57674
rs139471994	snp	C/T	0.0145793	0.0841255	synonymous-codon	RNF213	GRCh38.p7	17:80332268	GTTGCTGAGTGAGCC[C/T]GAAGAAGAATCAGAA	57674
rs139472659	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315405	GTGGTGGTGGTGGTG[A/G]TACTGGAGGTGATGG	57674
rs139478382	in-del	-/CTAA			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395664	GGGTACAGGTAGGAG[-/CTAA]CTAACTTCACCCCTG	57674
rs139518561	snp	C/G	0.0185938	0.0946107	intron-variant	RNF213	GRCh38.p7	17:80270812	GTTGCCCAAGTCCAG[C/G]CTTGAGGGGTTCAAG	57674
rs139568632	snp	A/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80349245	GACAGGTTTCTATGC[A/G]TCGTGCAGCTGGACG	57674
rs139610881	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268245	AATCGTGCTACAGTG[A/C]GCATGGGTGTGCATG	57674
rs139626034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377140	AAGGAGCTGGCACTC[C/T]GCCGGCTAGATGATC	57674
rs139639101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293536	TCGGTTAAAAGGGCA[C/T]GTGGTGGCTGGGCGT	57674
rs139646516	snp	A/G	0.000148443	0.0086139	synonymous-codon	RNF213	GRCh38.p7	17:80346387	TCCCGTCCTCTGGTC[A/G]TTGATGCTGGCCATC	57674
rs139646733	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379853	CATATTGAATAGCAA[G/T]GCCAAAGTCCCAGCA	57674
rs139654482	snp	G/T	0.000265766	0.0115244	missense	RNF213	GRCh38.p7	17:80317198	TGCAGGTCTGGAGGC[G/T]GCTGGTGGAAATCCA	57674
rs139675427	in-del	-/G	0.0456336	0.143994	intron-variant	RNF213	GRCh38.p7	17:80292771	GCCGCCTCCTCACCT[-/G]GGGGGGTCCTGGGCT	57674
rs139685293	snp	C/T	0.000990556	0.0222328	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386810	GGAGGGCAGAGAGAC[C/T]GTGCAGGAGTTCGAT	57674
rs139687165	snp	A/G	0.000164769	0.0090751	missense	RNF213	GRCh38.p7	17:80346097	GGACAACTGAGTGAC[A/G]TTGCTGAAAAGCTCT	57674
rs139701145	snp	C/T	3.34605e-05	0.00409012	synonymous-codon	RNF213	GRCh38.p7	17:80346666	CAGCTCCAAGTCTCT[C/T]GCCAAGACCATCGTG	57674
rs139726167	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80300535	AGGCATGAGCCACCA[C/T]GCCTGGCCTCATTGT	57674
rs139727178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343498	GCAGTTTCCTCCTTG[C/T]GTGAACGTCATGGTG	57674
rs139739751	snp	C/G/T	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388430	ACTCCGCTGGATTCC[C/G/T]GGTTGTGTTACTATT	57674
rs139754232	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314619	GTGGTGGTGGTGGTG[A/G]TGGTGGAGGTACTGG	57674
rs139766838	snp	G/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272798	GGGCGGGCAGATGCC[G/T]TAGTGCCAGGACAAG	57674
rs139774904	snp	C/G	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385105	AGGGATCTAGTGAAG[C/G]AGTTCCAGAACGTCC	57674
rs139778288	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272420	CATGGCAGAGTAGGC[A/C/T]GACGGGGATGCTGAC	57674
rs139806643	snp	A/T	0.0562307	0.157967	intron-variant	RNF213	GRCh38.p7	17:80300325	GCTGGAGTGCAGTGG[A/T]GTGATCTCAGCTCAC	57674
rs139810998	snp	G/T	3.29457e-05	0.00405854	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383784	CCCAGTGACCTTCCT[G/T]CCCCACCTGCCCCGG	57674
rs139812863	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80329418	ATGTATGGAGAAGTC[C/T]GATGCAGTGCCAGTT	57674
rs139820184	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372445	TTCTCCACAGTCACA[C/T]TGGCGACTGTAGAAG	57674
rs139825717	snp	A/G	0.142947	0.22592	intron-variant	RNF213	GRCh38.p7	17:80281321	ACATACCCCACTCAC[A/G]CCACTCACACACGCC	57674
rs139828251	snp	A/G	0.000881556	0.0209762	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353504	AATCACGTTTGCTTC[A/G]ACTGCAGTGGGCTTG	57674
rs139842089	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360486	TGGCCAGGGATATGG[C/T]GAAATGGGGTGTGTT	57674
rs139844147	snp	A/G/T	0.010732	0.0725379	intron-variant	RNF213	GRCh38.p7	17:80279381	TGGCGCTCGCCACGT[A/G/T]GGGGTGTAGTGGAAG	57674
rs139845061	snp	A/C/G	0.00159649	0.0282165	intron-variant	RNF213	GRCh38.p7	17:80310892	AGTTAGAACTGTGAC[A/C/G]TTAGTGATAGAAAAC	57674
rs139851661	in-del	-/C	0.0193772	0.0965046	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361025	TTGCATGCTCTGTGA[-/C]CCCCCAGCCCCTGAA	57674
rs139866938	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395454	GCACACAGAAAACAG[A/G]CTCTGCCTTCACATG	57674
rs139873121	snp	C/T	0.000362486	0.0134578	synonymous-codon	RNF213	GRCh38.p7	17:80345754	AAATGTGGCCTTCGC[C/T]AATAAGGACCAACAT	57674
rs139888585	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357505	TGTGCCTTCTTGTTT[A/C]GTTTGATCTGGGACA	57674
rs139891447	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80308885	TGAGATTTTCCAGAC[A/G]TTAACCTAGATAAGG	57674
rs139902060	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80311376	CTGAGCGGTCATTCA[A/G]TTTGTTGTTATTGGC	57674
rs139902431	snp	C/T	0.000181194	0.00951651	synonymous-codon	RNF213	GRCh38.p7	17:80345328	CAACGGCAGTGTCGA[C/T]GCCATCAGTCACTTG	57674
rs139906468	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259361	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATG	57674
rs139909020	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80349605	CCTCTCGGCCCCAGC[A/G]CTGCCGTGTTTTGGG	57674
rs139912986	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80290487	CGTGTGTGTGCGCAC[-/GT]GTGTGTGTGCGCGTG	57674
rs139929030	snp	A/G	6.5925e-05	0.00574092	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363205	ACCTTGCCTACCAGC[A/G]TTTCAGAAGCCGTCT	57674
rs139934539	snp	C/T	0.000798403	0.0199641	missense	RNF213	GRCh38.p7	17:80339274	ATATGCTGTTCAGGA[C/T]GTGGATCGCCATGGC	57674
rs139961057	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394811	TGAAGGGCAGAGTGA[C/T]CCAGACTGCAGGCAG	57674
rs139980431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270737	GACTGTTTATACTGG[A/G]AACAGCCTGAAACCC	57674
rs140013474	snp	C/T	1.64855e-05	0.00287097	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393484	GTGCTGAAATGGAAT[C/T]GAGAAATGAGATAGA	57674
rs140026874	in-del	-/ACAC			intron-variant	RNF213	GRCh38.p7	17:80281399	CCACTCACACCACTT[-/ACAC]ACCCCCAAGACAAAC	57674
rs140047947	snp	A/G	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80346909	CAAAATGCCCCTGAA[A/G]ACTCTGCACCCGCTG	57674
rs140056835	snp	C/T	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319740	GGAAAATTGTATCAA[C/T]TTATTTAGCTCTTTT	57674
rs140093141	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80271149	GGAGGGGCAGGCTCA[C/G]AATCCCTGGTTGTAG	57674
rs140103634	snp	G/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80317753	CTCTTAGCTCCGCCG[G/T]CTATGGACAGTAGTG	57674
rs140110990	snp	C/T	0.00041198	0.0143464	missense	RNF213	GRCh38.p7	17:80343996	GGACGTCAGTGCCGT[C/T]GAGGAGCTCTTCAGC	57674
rs140121978	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361078	TTACTTGGACCCGGG[C/G]GTTCCTGAAGCATGC	57674
rs140158248	snp	A/G	0.00139933	0.0264141	synonymous-codon	RNF213	GRCh38.p7	17:80344917	TGTCGAAGGCACCCC[A/G]GAGGAATGCCTCCAG	57674
rs140183688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264460	GCTTCTGGGGCCTCA[A/G]ACTGGTTCCCCTCCT	57674
rs140198244	snp	C/T	0.0023933	0.0345097	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398956	AACAAGGGCATATCC[C/T]GAAAGCACTGAGGCC	57674
rs140209733	snp	A/G	0.000148257	0.00860851	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375819	AACACTGTTTAGAGA[A/G]GTGGCTATTTTGTAC	57674
rs140244096	snp	C/G/T	0.00377158	0.0432621	missense, synonymous-codon	RNF213	GRCh38.p7	17:80343184	GAAGATGCAGTTAAA[C/G/T]GTGAAAAATGTGCCT	57674
rs140255873	snp	A/G	0.000131833	0.00811782	missense	RNF213	GRCh38.p7	17:80347729	AAGTACGTGGACCTC[A/G]GTCTGGGGACCCACC	57674
rs140300282	snp	A/G	0.00097292	0.0220344	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353538	CACCGGGCGGAAGAC[A/G]GCCATGAGGAGGCGA	57674
rs140329743	snp	C/T	0.000230597	0.0107352	intron-variant	RNF213	GRCh38.p7	17:80343842	TGTTTACACCTCGTG[C/T]GATTCTGTTCTTAGG	57674
rs140331722	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397263	CCAGTTCTACAGCCA[C/T]GGGCAAGTGGCTCGA	57674
rs140348297	snp	A/G	0.0267878	0.112589	intron-variant	RNF213	GRCh38.p7	17:80290966	GGTGTGTACCACCAC[A/G]CCTGGCTAATTTTTG	57674
rs140363426	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271332	TCACGAATTCTTGAG[C/T]TCTTGGCTACGCCAA	57674
rs140369116	snp	C/T	0.000925719	0.0214942	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288310	GGAGGCAGCTCTGAG[C/T]CCGGGACAGAACTGC	57674
rs140372966	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384317	CTCCCTGTGCCTAAG[A/C]ATCGAGGCGTACGTG	57674
rs140376240	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341390	AAAAAGAAATAGTAG[A/C]TTCTGTTCTGTTGAC	57674
rs140406954	snp	A/T	0.00447072	0.0470677	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367889	AAGGCGAGAATTCTG[A/T]ACCTCTCGTGGTTTT	57674
rs140432259	snp	C/T	6.58924e-05	0.0057395	synonymous-codon	RNF213	GRCh38.p7	17:80294869	AGCACCTTCAGCATC[C/T]TGCAGACCTGGGACA	57674
rs140435486	snp	A/G	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358162	GTTATTGCTGTCGCT[A/G]TAGTGTGGTAAATAG	57674
rs140466756	snp	C/T	0.000153988	0.00877328	stop-gained	RNF213	GRCh38.p7	17:80294962	ATGATTTATGAAGGA[C/T]AGGCACAGCTGTGGA	57674
rs140500651	snp	C/T	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382350	TCTTTTGCTAATCTG[C/T]AAAAATCACAATGAC	57674
rs140509634	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80278590	CACACCCTCCTGCCC[A/G]TGGGCCCTGGAGGCA	57674
rs140521485	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80328897	AACCACGAAAGAAAC[C/T]GTCATCATTTTACAA	57674
rs140560595	snp	A/G	0.021333	0.101051	intron-variant	RNF213	GRCh38.p7	17:80325857	CACATCAGGGAAGCT[A/G]TGGGGATCAAATAAC	57674
rs140649751	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80266291	TACAAAAAAAAAAAA[-/G]AAAAAAAAATACAAG	57674
rs140655993	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306017	TTTTTTAAAGTAGAG[A/G]CAGGGCCTCACTAGG	57674
rs140667469	snp	A/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385538	TATTCTGTTCAACAG[A/G]TGGGTTGAGGCAGCT	57674
rs140687760	in-del	-/TTTGTT/TTTTTTT	0.40086	0.199352	intron-variant	RNF213	GRCh38.p7	17:80265036	CCCAGTCCTTCCATG[-/TTTGTT/TTTTTTT]TTTGTTTGTTTTTTT	57674
rs140689095	snp	C/T	0.00159806	0.0282219	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364493	CGTGCTCCTAGGAAC[C/T]GAGAGCCGCGTCCCC	57674
rs140691890	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80302228	AGCAGTATGGAACGA[C/T]TGTAATTTACAATTT	57674
rs140695014	in-del	-/TC			intron-variant	RNF213	GRCh38.p7	17:80269599	TATCCGTCCATCCTA[-/TC]TGTTTATCTATCATC	57674
rs140698276	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355710	GGAATGGGGGCTTAC[A/G]GAGGAAGAAGCGGGG	57674
rs140718622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384969	CTCGCAGCCAGTCTC[A/G]AAGTCTGTAACCCCA	57674
rs140733234	snp	C/T	3.33962e-05	0.0040862	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376927	TTGCTGGCTCAAGCT[C/T]GGAGGTGGAAGGGTC	57674
rs140733783	snp	A/G	3.2975e-05	0.00406035	missense	RNF213	GRCh38.p7	17:80345419	CAGAGGGTGCCCTTC[A/G]ATGTCGACTTTGATA	57674
rs140757899	snp	C/T	0.00184362	0.0303053	synonymous-codon	RNF213	GRCh38.p7	17:80345637	TATTAAATTCCTTAG[C/T]GACCTGCGGCGTGGT	57674
rs140780402	in-del	-/TT	0.0715223	0.175059	intron-variant	RNF213	GRCh38.p7	17:80298647	AACTAACACACGCTC[-/TT]TTAACATTTTAAGAC	57674
rs140792335	snp	A/T	0.00755907	0.0610114	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397425	GAAATCCACAAGCAG[A/T]CAGCCTGCACCACAC	57674
rs140796877	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326634	TCTTTTCCAGAATGT[A/C]CTATGGTTGGAATCT	57674
rs140807350	snp	C/G	0.00141021	0.0265163	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288268	ACTGAAGATGCTGCC[C/G]AGGAGCTCCTGTTGC	57674
rs140818199	snp	G/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80337096	TCTGCTAGAAAGTCA[G/T]CAGAGTTTCCAAACA	57674
rs140822078	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80285808	CCCAAGTAGCTGGGA[C/T]TGCAGGTGCCTGCCA	57674
rs140866230	snp	A/T	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364926	ACCATTTTCATAGTC[A/T]TGGAGACAAGGATGT	57674
rs140907791	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320734	CTGGACACGGTTGCT[C/T]ACGCCTGTAATCACG	57674
rs140923376	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80334049	GTGCTTGCAGCTCAC[A/G]GATTCTGGGGTTCTG	57674
rs140934417	snp	C/T	1.65198e-05	0.00287395	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388630	ATACCCACTCTGGTG[C/T]ACAGACACGACTGGA	57674
rs140944665	snp	A/G	0.030665	0.119967	intron-variant	RNF213	GRCh38.p7	17:80289522	TTGAGCCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	57674
rs140980905	snp	A/G/T	0.00585636	0.0537948	synonymous-codon	RNF213	GRCh38.p7	17:80317223	AATCCAATTCCCCGC[A/G/T]GAGCATGGCTGGAAG	57674
rs140982903	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287101	CACGGTGGCTCACGC[A/G]TGTAATCCCACACTT	57674
rs141005604	snp	C/T	0.000297265	0.0121879	missense	RNF213	GRCh38.p7	17:80306440	TTTACTACCGGCTTC[C/T]GGGACTTGAGCAAGT	57674
rs141011780	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315147	GAGGTGATGGTGGTA[A/G]AGGTGATGGTGGAGG	57674
rs141041163	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384729	TCAGCAGCTTCTCTC[C/T]GTACCCAGCCAGTTA	57674
rs141059502	in-del	-/CA	0.41325	0.18934	intron-variant	RNF213	GRCh38.p7	17:80281338	ACTCACACACGCCCC[-/CA]CACACACACACCCCA	57674
rs141060237	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366901	ATTCCATTAGTACAG[C/T]CATTAAACTATCTTG	57674
rs141071032	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80266059	AGTAGTGTGGGCCCA[C/G]TAGCAGAGATTATGC	57674
rs141083276	snp	C/G	8.33285e-05	0.00645425	missense	RNF213	GRCh38.p7	17:80346547	CTGGACGGCGTACCT[C/G]TGAGGAAAACCATCG	57674
rs141089596	snp	C/T	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372590	CTAGAAGAGGAAGGT[C/T]GTTTCCTTAAGGCAT	57674
rs141109718	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80294061	TTACTTCTGTTTGTA[A/G]GTCTTCACGTGGCCT	57674
rs141120581	snp	C/T	0.000197661	0.00993939	missense	RNF213	GRCh38.p7	17:80306374	ATATGGAAAACTTCA[C/T]TGAGCACCTGGGTCG	57674
rs141120636	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80315551	GGAGGTGATGGTGGT[C/G]GTGGAGGTGATGGTG	57674
rs141121193	snp	C/G	0.00108678	0.0232853	intron-variant	RNF213	GRCh38.p7	17:80344665	CCATTTCATTAATGT[C/G]TCTCCTTTCCAGCGT	57674
rs141127877	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389623	GGCCCCTGCAAACAG[C/T]GTGATGTGAGCGGGC	57674
rs141142619	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80266690	TATTTTTAGTAGAGA[C/T]GGCGTTTCACCATGT	57674
rs141165583	snp	C/G/T	0.000511226	0.0159809	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351768	CAAAACTGTCCCGGG[C/G/T]GGGAAGAGGAACAGC	57674
rs141195915	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377990	AGGGCTTCTCAGACT[C/G]AGCACTGTGGACGTG	57674
rs141209499	snp	C/T	8.24205e-05	0.00641899	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386359	CTGTGCTACCGCTCT[C/T]GTCAGCTACTTGATT	57674
rs141224269	snp	A/C	8.24667e-05	0.00642079	missense	RNF213	GRCh38.p7	17:80313112	TCCGAGAAGTTTTTA[A/C]AAAGAACATGCTCAC	57674
rs141234263	snp	C/T	9.89691e-05	0.00703383	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358304	CACACCCTCTGGAAG[C/T]GGGTCCAAGGTGCTG	57674
rs141254099	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386176	TGATGGCTTCTGCAT[C/T]CCTCCTCCCCACGCC	57674
rs141301945	snp	C/T	0.00125711	0.0250395	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381662	ACAGTGCCGACGAGA[C/T]CATCGGCGTGGTCCA	57674
rs141327958	snp	C/T	0.00676609	0.0577691	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80362054	GGGGTCGCCCAGTCT[C/T]CTCTCAATATTCAGT	57674
rs141329059	snp	A/G/T	0.00503125	0.0499036	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373040	ATCCGGGTGGAGAAC[A/G/T]ACTGGCACCGGGTGT	57674
rs141334900	snp	A/G	0.000578527	0.0169979	missense	RNF213	GRCh38.p7	17:80346457	TATCGGAAAGCCATC[A/G]CCAGGTTCTTTCCGA	57674
rs141341964	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80329788	GTGAGCCGAAATCAC[A/G]CCACAACACTCCAGC	57674
rs141357091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307978	ATAGTCATGATACTG[C/T]ATATGCCTGGTGGGC	57674
rs141359625	snp	C/T	0.0460142	0.144533	intron-variant	RNF213	GRCh38.p7	17:80279621	AGGCACCTGCCACCA[C/T]GCCCGGCTACTTTTT	57674
rs141381946	snp	A/C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80277429	ATGGGGAAACCCCGT[A/C/T]TCTACTAAAAATACA	57674
rs141391616	snp	A/G	0.000515777	0.0160506	synonymous-codon	RNF213	GRCh38.p7	17:80347134	CCAAGGGTACTTTGC[A/G]TCCTTTGCCAAAGCC	57674
rs141400612	snp	A/G	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357695	AAAATAAAGCAGATA[A/G]GTGCGGTGGCTCACA	57674
rs141439032	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355795	TCATGGAGGAAAAAG[C/T]GGGGTGACCGGGAAT	57674
rs141454850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275493	AAATTTTGAAAAGTT[C/T]CCATGAATAATGAGG	57674
rs141491783	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298190	CTGCGTGAGTTAAAC[C/T]CTGCTCAGCCACGCG	57674
rs141509387	snp	A/G	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80283968	GTGGCTCACACCTGT[A/G]ATCACAGCACTTTGG	57674
rs141527929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365299	GCATGGATGCTGGAT[A/G]TGTTGACTCTGACCT	57674
rs141538163	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398721	GGAGTCAGAGAGAGA[A/G]AGAGAAAGAGACAGA	57674
rs141567136	snp	A/G	0.00130202	0.0254816	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363629	GGACGCATTTGCCGC[A/G]ATGGCCTGCACGGAG	57674
rs141576582	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352604	GCAGACCTTGCCAGT[A/G]TCCCCCACCCCTCAC	57674
rs141601980	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80313355	GAGGCAGACAGATGC[C/T]GGGTGCAAAGTGCTG	57674
rs141613575	snp	C/T	3.30639e-05	0.00406581	synonymous-codon	RNF213	GRCh38.p7	17:80298387	GTACACCTGGCTGGG[C/T]GCCCTGCCTGTCCTG	57674
rs141620585	snp	A/G	0.00151632	0.027493	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80288805	CCCTCTCCTGCCCAC[A/G]GCTGCGCCTCTTTCA	57674
rs141625043	snp	C/G/T	0.00322032	0.0399979	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360199	TCAGTACATCACAGA[C/G/T]GCAGAAGGTGAGGCT	57674
rs141652600	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80334379	CTTGGCCAAGGACTA[C/T]GTAAAGGGCAGAAAG	57674
rs141663890	snp	A/G	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360656	CAGGTGCCCCATCAG[A/G]AGGCACCTCCCAGCT	57674
rs141675700	snp	C/G/T	0.000263229	0.0114699	synonymous-codon	RNF213	GRCh38.p7	17:80343295	GTATCAGAAGGTCCC[C/G/T]GTGCTCTTTCACCTG	57674
rs141681070	snp	A/G	0.00028317	0.0118956	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372649	TGCCAACGAGGCCTC[A/G]GTTGAATACCTGCAA	57674
rs141686664	snp	C/T	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363157	AAGCGGCGTCAGAAG[C/T]GCCCGAGGAAGAGGT	57674
rs141715222	in-del	-/CTAT	0.0399052	0.1355	intron-variant	RNF213	GRCh38.p7	17:80269596	ATCTATCCGTCCATC[-/CTAT]CTGTTTATCTATCAT	57674
rs141739412	snp	C/G	0.0142736	0.0832652	intron-variant	RNF213	GRCh38.p7	17:80295087	TGACCCCTTGACTCT[C/G]TGGGCCAGGTTGCAA	57674
rs141825791	snp	C/T	4.948e-05	0.00497369	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386411	TACGCCGTGGAAAAA[C/T]TCTCCAAGGAAAACA	57674
rs141875024	snp	A/G	0.0182019	0.0936463	intron-variant	RNF213	GRCh38.p7	17:80299860	AGGATAATGGCCTCC[A/G]GCTCCATCTATGTTC	57674
rs141893340	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328622	TTTGCTGGGGGGATC[A/G]CTTTCACCTCTTTTA	57674
rs141894388	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286012	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	57674
rs141902510	snp	C/T	0.0150606	0.0854603	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382758	GTCTAAGATTACAAT[C/T]ATGTAGGATAGAGGA	57674
rs141921176	snp	A/G	0.00288552	0.0378739	synonymous-codon	RNF213	GRCh38.p7	17:80289835	CCAGGAAGTGAAGGC[A/G]AGGTAGGGATGCCCC	57674
rs141932054	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80297151	AGGCTCAACCCTTAC[A/G]TTTAAAAAGTTGTTT	57674
rs141934186	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327718	TGTGTTTGAGGAAGT[A/C/G]GGGGCAGAACAAGAG	57674
rs141936458	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270163	CCTGCGCATGCCTTG[A/C]TACTTTCATGTACAG	57674
rs141939582	snp	C/G	0.0182019	0.0936463	intron-variant	RNF213	GRCh38.p7	17:80338874	AATTGCTTGAACCCA[C/G]GAGGCAGAGGTTGCA	57674
rs141959953	snp	C/T	0.0142736	0.0832652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365856	CATAAGGGCCAGGTG[C/T]CCATAAACCCAAAGG	57674
rs141977905	snp	A/G	0.077417	0.180873	intron-variant	RNF213	GRCh38.p7	17:80271975	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAGAAGA	57674
rs141984643	snp	C/T	0.00153564	0.027667	intron-variant	RNF213	GRCh38.p7	17:80295506	AGCTCTGGACACTGC[C/T]GGTGAATTCAAGTCC	57674
rs142006531	snp	A/G	0.000399281	0.0141238	synonymous-codon	RNF213	GRCh38.p7	17:80325128	CTGGCCTAGGACCGC[A/G]GACAACTTCAATGAC	57674
rs142011336	snp	C/G/T	0.0134935	0.0810909	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378795	TGGTGTGTTATCAGC[C/G/T]GTGACTCTCAGTATA	57674
rs142017675	snp	C/T	0.00051175	0.0159879	missense	RNF213	GRCh38.p7	17:80298424	TGTATGGAGCTGGCC[C/T]CGCGGCACAAGGATG	57674
rs142018990	snp	C/T	0.000478126	0.0154543	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386732	TGAACTGCATGTCAT[C/T]AGTTATGAAGTGGAG	57674
rs142022751	snp	C/T	0.00368978	0.0427934	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288036	GCCACTGGAGGGTGA[C/T]GGCCTCTCCGCGCCC	57674
rs142036111	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213	GRCh38.p7	17:80351028	TCTGATGCTCTTAGA[A/G]TTAACTTTGTGCCTT	57674
rs142055624	snp	A/C/G	0.000592997	0.0172091	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376472	ATTCATGCTGCAGCC[A/C/G]TCCTTCTGTGTGGAC	57674
rs142074388	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366133	ACAAGAGGCTTGGGG[-/G]AAAGCCCTGCCTTCC	57674
rs142075904	snp	A/C/T	0.00034099	0.0130533	missense	RNF213	GRCh38.p7	17:80347262	ATAGAAAGCCTTCCC[A/C/T]GCAAGACATTGCACA	57674
rs142077875	snp	C/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388666	GAACATCTCTTTATG[C/G]ACATCAAGAACAAAA	57674
rs142078156	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80301228	CCCATTCCTATGTCT[A/G]GAATGGTATTGCCTA	57674
rs142078955	snp	G/T	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381232	TGTCTCTGGTCCACA[G/T]CTGGGAGTAGAGAGG	57674
rs142084040	snp	A/G	4.94939e-05	0.00497439	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390122	CGCCTTCCTGCTAGA[A/G]CTGCACGAAATGATA	57674
rs142096377	snp	C/T	4.94434e-05	0.00497184	synonymous-codon	RNF213	GRCh38.p7	17:80347695	ACTCAACCAGTACTA[C/T]GTCCACCTCGGCGGC	57674
rs142105290	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384491	AAACATTTCTCTCCA[C/T]GGACTATTATTTGCT	57674
rs142110800	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80295068	TGACCTGCTAGTGGC[C/T]GGATGACCCCTTGAC	57674
rs142120906	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389844	CCTTAAACAGATGCC[A/G]GTTAAAACACACCAT	57674
rs142133921	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259173	CCCAACTAGCGTTCT[A/C/G]AAGTGTCACCTTGGC	57674
rs142148113	snp	A/G	0.000329924	0.0128395	synonymous-codon	RNF213	GRCh38.p7	17:80291796	CGTCAACCGCTGTCT[A/G]TTCATAAAATCTTCA	57674
rs142165281	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80271179	GGTGAAACAGCAGCT[C/G]TCGAAGGATGGGGCC	57674
rs142169239	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373255	TACCCTCACACCCTA[-/C]CCCCCCCACACCCCA	57674
rs142182615	snp	C/T	0.0010373	0.0227503	synonymous-codon	RNF213	GRCh38.p7	17:80349802	GCTGCTAACAAGTCA[C/T]GACTGTGAAATTTTA	57674
rs142184116	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80347002	CTCCAACTGGGCCCT[C/T]GACCCTGCCAAGATG	57674
rs142229648	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380273	AGTGAGTGGGACCTG[C/T]GTGGGGGCCTCACAT	57674
rs142250065	snp	A/G	0.0158469	0.0875917	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390881	CAGCCTGGCCAACTG[A/G]TGAAACTCTGTTTCT	57674
rs142259702	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80267977	GGTGTGTGCCACCAC[A/T]TCCGGCTAATATTGT	57674
rs142287488	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80299681	TTAAGCCTAGTACCC[A/G]TTAGCTATTTTTCCT	57674
rs142287959	snp	C/T	3.29788e-05	0.00406058	synonymous-codon	RNF213	GRCh38.p7	17:80346360	CGTCAGCAAAAATCA[C/T]ACCGAGAGAGATCCC	57674
rs142310082	snp	A/G	0.000181286	0.00951894	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386376	TCAGCTACTTGATTC[A/G]CCTACACAATGAAAT	57674
rs142349792	snp	G/T	0.0475351	0.146656	intron-variant	RNF213	GRCh38.p7	17:80310455	ACAGGGTTTCACCAT[G/T]TTGGCCAAGCTGGTC	57674
rs142378840	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387623	AGGTTCTTCAGTCCA[C/T]GGCCTAAAACCCACA	57674
rs142382638	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393113	CTCCTGAGTAGCTTC[A/G]GACTATAGGCATACA	57674
rs142383457	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80311992	AATTAGCCAGGTATG[A/G]TGGCATGCACTTGTA	57674
rs142395128	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361661	ATTCCCCTTCACTCC[A/G]GAGCCCCCTGGAGGC	57674
rs142434537	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396236	CACTGCACTCCAACC[A/T]GGGTGACAGAGTGAG	57674
rs142436674	snp	C/G	0.0150606	0.0854603	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358863	GCAGTGAGCCGAGAT[C/G]GCGCCACTGCACTCC	57674
rs142450598	in-del	-/GCTGCC			intron-variant	RNF213	GRCh38.p7	17:80262879	TGAAGGCACCAGTCA[-/GCTGCC]GCTCCAGCCACTGCC	57674
rs142470190	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80309900	AGCTGGGACTACAGA[C/T]GCCTGCCACCACGCC	57674
rs142474750	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80310143	CTGAGCTCTGTCTGT[A/G]TGGTGCAGAGATCGG	57674
rs142491605	snp	C/T	0.000230916	0.0107427	synonymous-codon	RNF213	GRCh38.p7	17:80347464	GTCCCGCTACTTACT[C/T]GTGCTGACCAAAAAC	57674
rs142507915	snp	A/G	0.000411763	0.0143427	missense	RNF213	GRCh38.p7	17:80344723	GACATCTTCCCAAAA[A/G]TCACCTGCAGGCCTC	57674
rs142517970	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379932	GAAATGCAAAGCAGG[C/G]TACCCTTTAACAGCT	57674
rs142544809	snp	A/G	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80276936	GTGGCGTATGCCTGT[A/G]ATCCCAGCTACTTGG	57674
rs142567383	snp	A/C	0.0126979	0.078662	intron-variant	RNF213	GRCh38.p7	17:80284388	CAAAAACAAAAACAA[A/C]ACAAAAATAGCTGGG	57674
rs142599650	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80349807	TAACAAGTCACGACT[A/G]TGAAATTTTAGAATC	57674
rs142616352	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356007	TGCTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC	57674
rs142656779	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272912	AAAGCGTAACAGGCT[C/G]TGTTTTAGAGGTGCC	57674
rs142657947	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80284834	CGCCTCCTCTGGTGA[C/T]TGATTCCTCTGGAGA	57674
rs142702355	snp	C/T	0.00172832	0.0293458	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368024	CGTCTGTCTGCCCTG[C/T]GACCACGTGCACTGC	57674
rs142707121	snp	A/G	0.0142736	0.0832652	intron-variant	RNF213	GRCh38.p7	17:80263028	AAGCGCCCAAACGCC[A/G]TCTCCACTCTCACCC	57674
rs142714112	snp	A/G	0.000709202	0.0188175	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354419	ACGGCCATGCTGAAC[A/G]TCTGTTTCTGCCTTT	57674
rs142715215	snp	C/T	3.61827e-05	0.00425324	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287882	CAGAGCTGGCTTCCT[C/T]GCCCCTTTCTCCTGC	57674
rs142737038	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291469	CTCAAGAAGTCCTCC[C/T]GCCTCAGCCTCCCAT	57674
rs142742396	snp	A/G	0.0256215	0.110247	intron-variant	RNF213	GRCh38.p7	17:80272675	GGATGGACAAAGTGC[A/G]TCCACACCACAATGA	57674
rs142745586	snp	C/T	0.00795532	0.062565	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361505	CTCCAGCCTGGGCAA[C/T]AGAGTAAGACTCCAT	57674
rs142758536	snp	A/G/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319598	ACGGGCTTGCAGGCC[A/G/T]TTCCTCAGATGGCCC	57674
rs142796549	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280596	GTAGCTGGGACTACA[G/T]GCGTGCACCACCACA	57674
rs142798005	snp	C/T	0.000363696	0.0134802	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353039	TCAGCCAGCTGTTCG[C/T]GCCCGGAGACTTGCC	57674
rs142802614	snp	C/T	0.0622301	0.165053	intron-variant	RNF213	GRCh38.p7	17:80331539	GATTACAGGTGCGCT[C/T]CACCACGCCTGGCTA	57674
rs142823141	snp	G/T	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359790	GAACCAGAAGACTTG[G/T]TTCTGCCCGAGATTT	57674
rs142824974	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329178	GGTTCCCACGCCCCC[C/T]TCCCCCGCTACTCAC	57674
rs142826262	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80317663	GGCAGGAGCAAGCTC[C/T]GTGCAGGCCCTGCAG	57674
rs142863281	snp	A/G/T	0.00866673	0.0652553	intron-variant, missense	RNF213	GRCh38.p7	17:80278887	CTTGAGGCCGCCAGC[A/G/T]TGCCTTCTGCAGACT	57674
rs142869211	snp	C/G/T	6.59113e-05	0.00574038	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379620	CTGTCTTCACCCTAG[C/G/T]GTGGCAGGCCGATGG	57674
rs142873017	snp	A/C/T	6.74905e-05	0.00580873	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363717	AATCTTTCCATGCCG[A/C/T]TGGAGCTCATCTGCT	57674
rs142892282	snp	A/T	0.000307953	0.0124049	missense	RNF213	GRCh38.p7	17:80348011	TACCACTCGGACGCC[A/T]GCGCGTCTGTGGTGC	57674
rs142912858	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80281665	ACCCCACTCACACAC[-/A]CCCCAACATACGCAA	57674
rs142915137	snp	G/T	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356427	TCCGTCGTGTTCTGT[G/T]GTCACCGTGAGGCCT	57674
rs142915932	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393790	TAAACCAACATTGTT[C/T]ACATTCCAGGAGACT	57674
rs142936969	snp	C/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371100	CCAAATGACCAATGC[C/G]TGATGTCATGAAATC	57674
rs142961118	snp	A/G	8.46876e-05	0.00650666	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376949	GGAAGGGTCTGGAGC[A/G]AGTCCACTGGTACAG	57674
rs142962817	snp	C/T	4.95029e-05	0.00497484	missense	RNF213	GRCh38.p7	17:80263695	CCATGGAGTGTCCTT[C/T]GTGCCAGCATGTCTC	57674
rs143002142	snp	A/G	8.23703e-05	0.00641704	missense	RNF213	GRCh38.p7	17:80344679	TCTCTCCTTTCCAGC[A/G]TACACGTGTACCCCA	57674
rs143047595	snp	C/T	0.000594909	0.0172366	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374703	TGATGCAGCCCATCA[C/T]GTGACACTGTATTGG	57674
rs143060836	in-del	-/CACCC/CC			intron-variant	RNF213	GRCh38.p7	17:80311030	TGGCTGCTATTTAAA[-/CACCC/CC]CCGCCACAGGCAGCT	57674
rs143072652	snp	A/C/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80324594	AAAATATTGTTTCTC[A/C/G]GAGGAGAATTAAAAA	57674
rs143081354	snp	A/G	0.000494136	0.0157106	missense	RNF213	GRCh38.p7	17:80345638	ATTAAATTCCTTAGC[A/G]ACCTGCGGCGTGGTG	57674
rs143160659	in-del	-/TCCA	0.0744748	0.178019	intron-variant	RNF213	GRCh38.p7	17:80269565	CATCTATTCTATCTG[-/TCCA]TCCATCTATACTATC	57674
rs143163385	snp	C/G	0.000741491	0.0192405	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386387	ATTCGCCTACACAAT[C/G]AAATTGTCTACGCCG	57674
rs143170125	snp	A/G	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80309019	TCTTTGCGGGGCAGG[A/G]TTCCCGAGGAGGCCT	57674
rs143174393	in-del	-/GT	0.487746	0.0773096	intron-variant	RNF213	GRCh38.p7	17:80274969	TTGGGGTGTGTGTGT[-/GT]TGGATGTGTGTGTAT	57674
rs143184273	snp	C/G	0.00103411	0.0227153	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287858	AGAAGGGGAACAAGT[C/G]CGCTTCCTCAGAGCT	57674
rs143186348	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80266139	GGTTGGCTGAAACAT[C/G]GATCAAAAGGTGGCC	57674
rs143189961	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213	GRCh38.p7	17:80292045	TCTCCTTTGAGCTCA[A/G]TGTGACTTACCTACT	57674
rs143208661	snp	C/T	0.000806976	0.0200708	missense	RNF213	GRCh38.p7	17:80345663	GTGGTGGTACCAATG[C/T]TGACACCATAAAGCT	57674
rs143251320	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375618	GGCTGAGTTAGAATC[G/T]CTTGAACCCGAGAGG	57674
rs143251369	snp	G/T	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80342825	ATGACAACTGCACCC[G/T]AAGGGATGTCTTAAG	57674
rs143262287	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303296	GGAGAACAGAGGTAA[A/T]GACTGCAGCACTCTG	57674
rs143274853	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310930	TGTATGTTTTAACTT[C/T]CTTCCTTTCAGTTTT	57674
rs143280632	snp	C/T	0.0244538	0.107838	intron-variant	RNF213	GRCh38.p7	17:80331220	CTGCTTTTTGGGAAT[C/T]CTGTGACATAAAACT	57674
rs143282038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289535	GCGGAGGTTGCAGTG[A/G]GCTGAGATCGCAGTA	57674
rs143300859	snp	C/G	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80312051	GAGGATCACTTGAAC[C/G]CAGGAGGTGGAGGTT	57674
rs143302645	snp	C/T	8.32438e-05	0.00645097	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363112	CCCAGTTTCTGCAGA[C/T]GGCTCTGTGGTCCTG	57674
rs143335048	snp	C/G	1.75545e-05	0.00296259	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372560	GCTTACTCCAGAAAT[C/G]ATGAACTGAACCACC	57674
rs143336602	snp	C/G	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80272182	CCAGCTACTTGGGAG[C/G]CCGAGGCAGGAGAAT	57674
rs143340263	snp	A/T	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369624	TGATTGAGAGCCTGC[A/T]CTCTCTCCTCTTCGT	57674
rs143355634	snp	C/G	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80298954	ACTGCACTGTAGCTT[C/G]GGCGACAGAGCGAGA	57674
rs143360509	snp	A/G	0.000215573	0.0103798	synonymous-codon	RNF213	GRCh38.p7	17:80295646	GCCTGTGGACTGCCC[A/G]GTGAGGAGTAAACTG	57674
rs143360856	snp	A/G	0.0142736	0.0832652	intron-variant	RNF213	GRCh38.p7	17:80279666	TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC	57674
rs143362943	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351918	GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTAC	57674
rs143364493	snp	A/G	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80295724	ATTAGAAGGCAGCCT[A/G]GACTGGTTGTGTCAC	57674
rs143369201	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80317909	AAGAATGGGGTCACC[C/T]GGACACTTGAAGGAT	57674
rs143381302	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381937	CTCTGCTTGCCCAGA[A/G]GCTGGAAGGAGCTGC	57674
rs143394069	snp	C/G/T	0.00133395	0.0257941	missense	RNF213	GRCh38.p7	17:80343984	TCCTGGAAAGGAGGA[C/G/T]GTCAGTGCCGTCGAG	57674
rs143410054	in-del	-/TG	0.127944	0.218179	intron-variant	RNF213	GRCh38.p7	17:80262000	CAGCCTGGGTGAAAC[-/TG]TCAAACAAACAAAAA	57674
rs143413764	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315626	GATGGTGGTCCGTGG[A/T]GGTGATGGTGGTGGT	57674
rs143425566	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316583	GGGGGTGGAGACCAC[G/T]TCCTGGGGGCAGAGT	57674
rs143426057	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80315352	TACTAGAGGTGATGG[C/T]GGTCGTGGAGGTGAT	57674
rs143427383	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392974	TGATTGGTCCCCTTA[C/T]GTTATATGGGAGCCT	57674
rs143428968	snp	C/T	0.000824225	0.0202838	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367762	GTGTCTTCGAGAGAA[C/T]TCTGACGTGAAGACG	57674
rs143472355	snp	A/G	0.00376334	0.0432147	synonymous-codon	RNF213	GRCh38.p7	17:80347125	GGACCGAGTCCAAGG[A/G]TACTTTGCGTCCTTT	57674
rs143485810	snp	C/T	0.00231885	0.0339713	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354156	CTTGAATGAGGATGA[C/T]GCGTGCCACGGTATG	57674
rs143491577	snp	C/T	0.000527435	0.0162308	synonymous-codon	RNF213	GRCh38.p7	17:80346345	TCTCTCCAAGTCCAG[C/T]GTCAGCAAAAATCAC	57674
rs143510179	in-del	-/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80315620	GGAGGTGATGGTGGT[-/C]CGTGGAGGTGATGGT	57674
rs143520187	in-del	-/TCCA			intron-variant	RNF213	GRCh38.p7	17:80268610	TCATCCATCTGTTTG[-/TCCA]TCCATCCATCCATCC	57674
rs143527185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364799	TTCCAGGAACTGTGT[A/G]CAGAAAGGGGCTGAC	57674
rs143529570	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80314368	TACTGGAGGTGATGG[C/T]GGTCGTGGAGGTGAT	57674
rs143570601	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315210	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs143571724	snp	A/G	0.0479149	0.147179	intron-variant	RNF213	GRCh38.p7	17:80267132	TGAGGCACAAGAATT[A/G]CTTGAACCCAGGAGA	57674
rs143580800	snp	C/T	0.000560778	0.0167354	synonymous-codon	RNF213	GRCh38.p7	17:80346402	GTTGATGCTGGCCAT[C/T]GGGGTGTGTTACCAT	57674
rs143583853	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80281219	ACTCACACACACCCC[-/CA]CACACACCCCACTCA	57674
rs143603857	snp	A/C	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80307628	CATCTTGGCTCACTG[A/C]AACCTCTGCTTCCCA	57674
rs143618176	snp	A/T	0.0678174	0.1712	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356202	AGGCGAGATTTCACC[A/T]TGTTGGCCAGGCTGG	57674
rs143639056	snp	G/T	3.29451e-05	0.00405851	missense	RNF213	GRCh38.p7	17:80306357	GAGTCACCTGGTTAT[G/T]TATATGGAAAACTTC	57674
rs143657240	snp	C/G	0.0158469	0.0875917	intron-variant	RNF213	GRCh38.p7	17:80293180	CTCCCCCTCAGCCCC[C/G]CCAAGTAGCTGGGCC	57674
rs143681826	snp	C/T	0.00165207	0.0286933	intron-variant	RNF213	GRCh38.p7	17:80327787	AGGTGGGGAGCCCAC[C/T]GTGTTAACTGTGTTC	57674
rs143694282	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80304437	CAAGGTCAGGAGATC[A/G]AGACAAGCCTGGCTA	57674
rs143695400	snp	C/T	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80290895	GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA	57674
rs143699710	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320010	TCCTTTCCCTTTTTC[A/G]TTAACTCTTTGTTGA	57674
rs143701682	snp	A/G	0.0205511	0.0992634	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355879	CTTCCTCGTGACCAG[A/G]GATTTTCTGATTCTA	57674
rs143721660	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80285375	CTGCATGGCAGCCCC[A/G]GAGGTACCAGGCAGC	57674
rs143755370	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386540	ACAGACACTCACTCC[C/T]TCAGCCGCCCCCACC	57674
rs143766322	snp	A/G	0.00019771	0.00994062	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383898	AAATGGCAAAGAAAG[A/G]GTGCCCATCCTCTGG	57674
rs143772929	snp	C/T	0.000214209	0.0103469	synonymous-codon	RNF213	GRCh38.p7	17:80345751	TGAAAATGTGGCCTT[C/T]GCCAATAAGGACCAA	57674
rs143778568	snp	A/G	3.30688e-05	0.00406612	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353038	ATCAGCCAGCTGTTC[A/G]CGCCCGGAGACTTGC	57674
rs143787564	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378655	TATAAGAGATACGGA[A/G]GGAGAAAAACTGTTA	57674
rs143788277	snp	A/G	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80322933	GCTTGTACTTTTGGT[A/G]TCAAAGAATCCTTTG	57674
rs143788782	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80332872	CTGCGTGAAGATCAA[G/T]AACTCAGGAAAGGGC	57674
rs143804219	snp	A/G	8.24328e-05	0.00641947	missense	RNF213	GRCh38.p7	17:80345831	CTATAAGCTGTATCA[A/G]AGAAGTCCTGTGTGA	57674
rs143806303	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80323979	TCAAATTGTGTGTGC[-/GT]GTGTGTGTGTGTGTG	57674
rs143828863	snp	A/G	0.000248318	0.0111399	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369804	CTCTCTCTCCATTCA[A/G]TGATGTTGTGGATAA	57674
rs143887157	snp	A/G	0.000625813	0.0176781	missense	RNF213	GRCh38.p7	17:80309133	CCAGCCTTATCTGCC[A/G]AGATTGTCTGCAGAA	57674
rs143887567	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280484	TTTGAGGCAGGGTCT[C/T]GCCCTGGGTCCCAGG	57674
rs143904490	snp	C/T	0.00108687	0.0232863	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379666	TTGACTGCCATGCGC[C/T]GATTGGAGGCATTGA	57674
rs143918463	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357932	ATTCCAGGTTATGAC[A/G]ATCTATGATTGTGTC	57674
rs143933797	snp	A/G	0.0138799	0.0821421	intron-variant	RNF213	GRCh38.p7	17:80278439	GTGTGGAGGCCCGGG[A/G]CGCCGGGAGCCTGGT	57674
rs143949169	snp	C/T	0.00716266	0.059414	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357457	AGTGTACAAAAACAT[C/T]AACAGGAACAAATAC	57674
rs143957146	in-del	-/TTCT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365433	GTCAGGTGCCCACGC[-/TTCT]TCCGTCTTGTCCCTT	57674
rs143959110	snp	A/C/T	0.000164967	0.00908056	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364535	GCTGGTGACCGAGCA[A/C/T]GTCTTCTTACTAGAC	57674
rs143979980	in-del	-/ACTT	0.0475637	0.146695	intron-variant	RNF213	GRCh38.p7	17:80273197	TCCTTCCTAACACTC[-/ACTT]GCTTCTCTCTGAGAT	57674
rs144007255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308710	TTTCAAATTTATGTC[A/G]TATTTTAATGTCTAG	57674
rs144040476	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380047	TCACGAGGACATCTA[C/T]GTCTGCAGGACCAAA	57674
rs144053288	snp	A/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80335268	CTCCATTGATGCTGT[A/G]CGTTTCTTGGCAGCC	57674
rs144070062	snp	A/G	0.000132286	0.00813176	synonymous-codon	RNF213	GRCh38.p7	17:80348175	GGGCGGGTTCGCAGC[A/G]GAGTGGCTGTCGCAG	57674
rs144074554	snp	C/T	0.00136978	0.0261346	missense	RNF213	GRCh38.p7	17:80346445	AAGAAAGACTCATAT[C/T]GGAAAGCCATCGCCA	57674
rs144083500	snp	C/T	0.000742078	0.0192481	synonymous-codon	RNF213	GRCh38.p7	17:80313152	TGCCTCATTCACATA[C/T]GTCAAGGAAATTGAG	57674
rs144098631	snp	C/T	0.00957433	0.0685237	synonymous-codon	RNF213	GRCh38.p7	17:80346165	CAGCCTAGATGAAAA[C/T]GGGACTCGCGTGATC	57674
rs144121398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344209	GATAAAAGTACTCTT[C/T]TGTTAATTAGCAGTG	57674
rs144121700	snp	G/T	0.00121367	0.0246041	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376976	ACAGTAAGTGTTGGG[G/T]TCTAGATGACCCCAC	57674
rs144130028	snp	C/G	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80334550	TCCTTAAAATCTTGC[C/G]CCCTTCAGCTTTTTC	57674
rs144139703	snp	C/T	0.000918737	0.0214132	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353530	GCTTGGAACACCGGG[C/T]GGAAGACGGCCATGA	57674
rs144153981	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80298498	CTCCTTCTCACCGTT[C/T]CGGGAACAAATGCTA	57674
rs144159221	snp	C/T	0.00953873	0.0683987	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320777	CCCAGGAGTTCAAGA[C/T]AAGCCTGGGTAACAG	57674
rs144160370	snp	C/G/T	6.96274e-05	0.00589996	missense, stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372992	ATGGCCAAGGAGAAG[C/G/T]AGTGCTACCTGCAGC	57674
rs144162402	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80283764	GGGCTCCTCCTGTTC[C/T]GGGCTGTGACTCGGC	57674
rs144174438	snp	A/C	0.000155337	0.00881161	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288136	GCTCAGAGCAGCCCG[A/C]AATTCCAGGACCACA	57674
rs144219136	snp	C/T	0.0012349	0.0248179	synonymous-codon	RNF213	GRCh38.p7	17:80346255	TGTCAGCCTCAGGGA[C/T]GTGGAGCGCTGTGTG	57674
rs144239294	snp	C/T	0.0415807	0.138063	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376279	TTTGATACATCTTAA[C/T]GTTAAGTTTTTTTCC	57674
rs144262057	snp	C/T	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80270885	GCCCTTCTCCACTGC[C/T]AGCTTTGTCTGCAGG	57674
rs144268610	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80265046	TCCATGTTTGTTTGT[G/T]TTTTTTTTTTTTTTT	57674
rs144293459	snp	A/C	0.000307953	0.0124049	missense	RNF213	GRCh38.p7	17:80345893	GACTCTGGCCTGCAT[A/C]TTATAGCTGCCTGCA	57674
rs144304327	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268289	AGCCCAGGAGGTCAA[C/T]GCTGCAGTGAGCCGT	57674
rs144322135	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80342328	TAGTGCTAAGTGGCG[C/T]GGGACTCTGCTTTGC	57674
rs144359866	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357628	TTATTTAGAGAACCT[C/T]GATGACTTGTTCTGA	57674
rs144365431	in-del	-/CCCCCCCACCC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396727	CAGGAAAGTGCATTT[-/CCCCCCCACCC]CCCCCCCCCAACCAG	57674
rs144367158	snp	A/C/G/T	0.00111168	0.0235509	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386849	GATTCAGCGGCAGAT[A/C/G/T]GTCAGCCGCTTCCTC	57674
rs144374952	snp	C/T	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80346692	TCGTGGCAGACGCCA[C/T]GCAGGGCCCGGCTGC	57674
rs144383562	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355704	TGACCGGGAATGGGG[G/T]CTTACAGAGGAAGAA	57674
rs144391484	snp	C/T	0.00466888	0.0480899	intron-variant	RNF213	GRCh38.p7	17:80308984	GCTTCTCCTAAATCC[C/T]TGCCGGGATTTCTCT	57674
rs144398532	snp	C/T	0.0174175	0.0916809	intron-variant	RNF213	GRCh38.p7	17:80267755	CTGCTGGAGAAGCTG[C/T]AGTAAGTTCTCCAGA	57674
rs144444568	in-del	-/CTTTTCTTTTTT			intron-variant	RNF213	GRCh38.p7	17:80303545	AAACCAATTCTATTC[-/CTTTTCTTTTTT]CTTTTCTTTTCTTTT	57674
rs144452483	snp	A/G	0.0418186	0.138422	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390611	TGTGTTGGCCAGGCT[A/G]GTCTCGAACTCCTGG	57674
rs144458310	snp	A/G	6.61638e-05	0.00575131	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363132	CTGTGGTCCTGCACT[A/G]GGAAACTGAAAGCGG	57674
rs144489370	snp	A/C	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387461	ACCCCCACAGCCCCT[A/C]TTCCTTCAGCCTCCA	57674
rs144504639	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80263850	CACCTCCCTTCCAGG[A/G]AATGGAAACCCTGGG	57674
rs144518053	snp	A/C	0.000329435	0.01283	synonymous-codon	RNF213	GRCh38.p7	17:80346156	TGAGTCCATCAGCCT[A/C]GATGAAAACGGGACT	57674
rs144520262	snp	A/G	0.000565102	0.0167998	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386846	GAAGATTCAGCGGCA[A/G]ATCGTCAGCCGCTTC	57674
rs144523910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272855	CCACTGGGAGAATGC[C/T]CACCCTGGGGAAGAC	57674
rs144538021	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80325883	ATAACTGAATTAATA[C/T]GGGAGTGCACAAGTA	57674
rs144566232	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80315395	GGAGGTGATGGTGGT[C/G]GTGGTGGTGGTACTG	57674
rs144573494	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280868	AGCTGTCAACGTACA[C/T]GGGTGGAAACATTCC	57674
rs144576626	snp	C/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80336719	ATTTTCTATAATTGA[C/T]AGAATTTTTTATCAG	57674
rs144576944	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366911	TACAGCCATTAAACT[A/G]TCTTGTACAGTGATG	57674
rs144582733	snp	C/T	0.000307953	0.0124049	missense	RNF213	GRCh38.p7	17:80343225	TTCGACTGATCGACC[C/T]TCAGGTGGATGAGAG	57674
rs144586324	in-del	-/CTCCCGGCGATGC	0.0158469	0.0875917	intron-variant	RNF213	GRCh38.p7	17:80278229	GTCTTGCTGTGAGGT[-/CTCCCGGCGATGC]CCGGTGTGGTGTGGA	57674
rs144609836	snp	A/G	0.00914312	0.0669923	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397464	TGGTAGTTAAAGATC[A/G]ACGCCTGACCTAATC	57674
rs144625219	snp	A/G/T	0.000148252	0.00860858	missense	RNF213	GRCh38.p7	17:80345042	CCTCTCTCTTCTGCA[A/G/T]TCCGAGTTTTATTGG	57674
rs144625692	snp	A/C	0.0158469	0.0875917	intron-variant	RNF213	GRCh38.p7	17:80341997	AGAGATGGGGTTTCA[A/C]CATGTTGGCCAGGCT	57674
rs144662350	snp	C/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80317435	GATCCAGCCCTTATA[C/G]TCTGTCCCTAGAAGA	57674
rs144664526	snp	C/T	0.00522971	0.0508675	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364502	AGGAACCGAGAGCCG[C/T]GTCCCCGAGTTACAG	57674
rs144712336	snp	A/G	1.67097e-05	0.00289043	synonymous-codon	RNF213	GRCh38.p7	17:80346639	TCCCCTCTTCCTGGT[A/G]GGGAAGCCCGGCAGC	57674
rs144719362	snp	C/G/T	0.00028013	0.0118317	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369524	ATTGAAAAGCATGCC[C/G/T]GCTTCCGGCAGATGT	57674
rs144721501	snp	A/G/T	0.000167652	0.00915432	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373097	CGGGGGATGGAGTTC[A/G/T]TGCAGGGCCTCTCCA	57674
rs144731803	snp	C/T	4.94279e-05	0.00497107	intron-variant, missense	RNF213	GRCh38.p7	17:80319338	TCTCCTCCTGGGAAA[C/T]GGATTCGGGCTCACA	57674
rs144767827	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365646	ACTGAGGAGTTTTTC[A/G]TGGCATGGTCATGTT	57674
rs144769597	snp	A/T	0.00278404	0.0372058	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288179	ACCAGGACGCTTCCA[A/T]CCCCTCTGGGGGCAG	57674
rs144803027	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80263909	CCTCTGTGGCTACTG[A/G]GGCTCTGTGGCTCTG	57674
rs144809290	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355707	CCGGGAATGGGGGCT[C/T]ACAGAGGAAGAAGCG	57674
rs144814798	snp	A/G	3.30224e-05	0.00406326	synonymous-codon	RNF213	GRCh38.p7	17:80347395	GCAGCTGATCAAACA[A/G]AACATCTTTGGGCCT	57674
rs144839736	in-del	-/ATCT			intron-variant	RNF213	GRCh38.p7	17:80268653	TTATCTGTCTATCTA[-/ATCT]TCTGTCATCTGTCTT	57674
rs144859733	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395235	TATACTGGCCTAGCA[A/G]AGGCAAAAAAAAAAA	57674
rs144870684	snp	A/G	9.88908e-05	0.00703105	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351765	TCACAAAACTGTCCC[A/G]GGTGGGAAGAGGAAC	57674
rs144875443	snp	C/G	0.184203	0.241186	intron-variant	RNF213	GRCh38.p7	17:80318636	TGGAGTGCAGTGGCG[C/G]GATCTCGGCTCACTG	57674
rs144882669	snp	C/T	8.24205e-05	0.00641899	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380933	AGTGGTCTTCCTCCT[C/T]ATCCGGCTACTCACT	57674
rs144887674	in-del	-/TATT			intron-variant	RNF213	GRCh38.p7	17:80325938	TTTTTGTGTTATTTG[-/TATT]TATTTATTTATTTAT	57674
rs144899673	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329675	CTCTAAAAAAAATAC[A/C]AAAAAATTAGCAAGA	57674
rs144912419	snp	C/G/T	4.94184e-05	0.00497063	missense, synonymous-codon	RNF213	GRCh38.p7	17:80290606	AGTCACCGTGTTCTT[C/G/T]CACGCCATCATCTCT	57674
rs144915128	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279218	ACACCTGGAGAAACT[C/T]AACCTGGCTGCACTC	57674
rs144930750	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287307	TCAAAACCAGCTTGG[A/G]CAACATGGTGAAACC	57674
rs144941559	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80324637	GTATATGTTGTTTGT[A/G]GGCAGCTTTTTAAAA	57674
rs144944826	snp	C/T	0.000227998	0.0106746	missense	RNF213	GRCh38.p7	17:80339349	GCTTGGACCTGGTGA[C/T]GGAGCTTAAAGAAGG	57674
rs144988652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384092	GCTAGAGATCTTCAT[A/G]CATATCAAACTGTAT	57674
rs145017985	snp	C/T	0.00118561	0.0243187	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288739	CAACCACTCCTCCTT[C/T]CAAAACACACTGCCA	57674
rs145019092	snp	C/T	0.000776109	0.0196838	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358474	TCTTGTGATGAATAA[C/T]GAAAGGTGAGTGGAA	57674
rs145021197	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80298214	CCACGCGCGGTGCTC[C/T]TCTTGCTCTGTGTGC	57674
rs145028335	snp	A/G	6.5937e-05	0.00574144	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353613	GAGGAGGCCATGGAA[A/G]CAGAAAGTTCTGAGA	57674
rs145055003	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326278	TCCAGGCGTGCACCA[C/T]CATACCCAGCCTGTT	57674
rs145066039	snp	A/G	6.59935e-05	0.0057439	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352973	ACATCGATGACCTCC[A/G]GAGATCCACCCTCAT	57674
rs145076497	snp	A/G	0.00642191	0.0563002	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380972	TCTGCTTCTGGGAGC[A/G]TCCCAGAGTTCCCAG	57674
rs145120787	snp	A/G	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374189	CCTCAGGTGTGGTGC[A/G]GTGCGCCGCAAACGG	57674
rs145156874	snp	A/G	6.58979e-05	0.00573974	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375782	AGACCCCCCAAAGCC[A/G]GCAGTCAGCCTACTT	57674
rs145164928	in-del	-/ATAAC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396275	CAAAAAAAAATAAAA[-/ATAAC]TAAGGACCTTATTGT	57674
rs145172026	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80327631	GAATCTGGGCAAGAC[C/T]TAACCCTCGTGGGGG	57674
rs145176053	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277489	TGTAATCCCAGCTAC[G/T]CAGGAGGTTGAGGCA	57674
rs145192984	snp	C/T	0.000826202	0.0203081	intron-variant	RNF213	GRCh38.p7	17:80337566	ACCGTGGCCCGTGTT[C/T]TCTCCTTTTGTCCCC	57674
rs145210854	snp	C/T	0.00148165	0.0271778	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368030	TCTGCCCTGCGACCA[C/T]GTGCACTGCCTGCGC	57674
rs145237547	snp	A/G	0.00812851	0.0632312	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287795	TAAGAAATAAAGTGA[A/G]TGTCTCTCTTTCTGT	57674
rs145246688	snp	C/T	0.0158469	0.0875917	intron-variant	RNF213	GRCh38.p7	17:80340681	GCTGGAGTACAGTGG[C/T]GTGATCTTAGCTCAC	57674
rs145251836	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313808	GGTGATGGTGGAGGT[A/G]ATGGAGGTGATGGTG	57674
rs145279702	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367682	TGTGGTGCTCCCTCT[A/G]TCGCCCGGCCTGGCC	57674
rs145282452	snp	A/G	0.000230677	0.0107371	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380889	CCGCAGCGGAGAGAC[A/G]TGGTGACATGTGACC	57674
rs145284392	snp	A/G	6.59337e-05	0.0057413	synonymous-codon	RNF213	GRCh38.p7	17:80343997	GACGTCAGTGCCGTC[A/G]AGGAGCTCTTCAGCG	57674
rs145284893	snp	A/G	0.000131776	0.00811608	synonymous-codon	RNF213	GRCh38.p7	17:80345235	GAAGAGGTGGGAGTC[A/G]GAGCCTCACCCATAC	57674
rs145288878	snp	A/G	0.0185938	0.0946107	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365390	GCAGCCCAAGGCTAA[A/G]GTACCAGCTCCCCGG	57674
rs145299917	snp	C/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80300625	GTGGCACAATCTCAG[C/T]TCACTGTAACCTCTG	57674
rs145307523	snp	C/T	3.3543e-05	0.00409516	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372691	GATCCGCCTCTGCCT[C/T]GACAGAGCTGCAGAT	57674
rs145313049	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281338	CACTCACACACGCCC[A/C]CACACACACACCCCA	57674
rs145323444	snp	A/G	0.00716266	0.059414	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398957	ACAAGGGCATATCCC[A/G]AAAGCACTGAGGCCT	57674
rs145348848	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261267	GGGACAGCCGGACCC[A/G]GGCCTGCAGGTCCGC	57674
rs145355706	snp	G/T	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80327434	TACAGTGGGCTATGG[G/T]TGTGCCACTGCACTC	57674
rs145365075	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381421	CTGGATCACTCCGCC[A/G]TTTTCATCTTAGAAA	57674
rs145373018	snp	A/G	9.88338e-05	0.00702902	synonymous-codon	RNF213	GRCh38.p7	17:80343904	GCTCCTCATTTTACA[A/G]TACTTAATGGATATA	57674
rs145376191	snp	C/T	0.02016	0.0983543	intron-variant	RNF213	GRCh38.p7	17:80340663	TCTTGCTCTGTCACC[C/T]AGGCTGGAGTACAGT	57674
rs145385681	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395551	GCCACTCCCTGTAGC[C/T]GATCTGGGACTGAAA	57674
rs145402736	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390805	GTGGAGGCTTACCCT[A/G]TAATCCCAGCACTTT	57674
rs145435944	snp	A/G	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80276677	TGTGGAGAAATTGGA[A/G]GTGTTGTACAGTGTT	57674
rs145448552	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	RNF213	GRCh38.p7	17:80346261	CCTCAGGGACGTGGA[A/G]CGCTGTGTGAAAGTT	57674
rs145449127	snp	A/G	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80265384	AATAGTGCGGAGAGC[A/G]CTGGTAGTGCGCAGC	57674
rs145456322	snp	C/T	0.00031295	0.0125051	synonymous-codon	RNF213	GRCh38.p7	17:80345316	GCAGCCCAACATCAA[C/T]GGCAGTGTCGATGCC	57674
rs145473499	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377866	GAGGAGGGGGATCGT[A/G]GGTCAGGAGAGTGAG	57674
rs145480652	snp	A/G	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80305458	GCTGGGATTACAGAC[A/G]TGAGCCACTGCGCCC	57674
rs145490620	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262348	CCTATTGGGAACCTC[A/C]TCAAAGAGAAGACTG	57674
rs145543645	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80341501	GACTTTTATTAGCTA[C/G]TCACTCAACACATAA	57674
rs145553991	snp	A/C/G	4.942e-05	0.00497071	synonymous-codon, missense	RNF213	GRCh38.p7	17:80294889	GACCTGGGACACCAT[A/C/G]AACCTGAACAGCTTC	57674
rs145581088	snp	A/C	1.64789e-05	0.0028704	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288586	ATTGAGTCGGAGTCA[A/C]CCTGGCCCATTTTGT	57674
rs145599764	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389907	CTGAACAGCTGCTGC[A/G]GCTGCACAAAGTAAG	57674
rs145606699	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80269151	GCTTTGTTCTAGCCA[C/T]GCTGGCAGCTGACTG	57674
rs145622326	snp	A/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352677	CCACAGGCCTTATCC[A/G]TGCGTCCTTCCCACG	57674
rs145623354	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384976	CCAGTCTCAAAGTCT[A/G]TAACCCCAATAACAT	57674
rs145633285	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80267713	GTCATCTCCATAACA[C/T]AAAAGTGCAAGGTGA	57674
rs145638043	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375542	CCGTGTCTACTAAAA[A/G]AAAAAAAAAAAGAAT	57674
rs145642913	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382675	CAGCTGAGACGGCTG[A/G]CGGTAGCCTGGGCCA	57674
rs145670917	snp	A/C/G	0.000515927	0.0160531	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390178	CCCAAACCGAGGAGC[A/C/G]CTTCCGCCCTCAGTG	57674
rs145673558	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264736	ACAGACCCCCTTACA[A/G]GATCCGCCCCTGCCC	57674
rs145731088	snp	A/G	5.00154e-05	0.00500052	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363641	CGCAATGGCCTGCAC[A/G]GAGATGCTGACAAGA	57674
rs145741591	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388941	CTGCTGAAGCGGGAA[G/T]TCCATGGAACCGATT	57674
rs145752865	in-del	-/GGG	0.0454132	0.143681	cds-indel	RNF213	GRCh38.p7	17:80348183	CGCAGCGGAGTGGCT[-/GGG]GTCGCAGGAGTACTT	57674
rs145779158	snp	A/G	0.00259936	0.0359573			GRCh38.p7	17:80343839	GTGTGTTTACACCTC[A/G]TGCGATTCTGTTCTT	57674
rs145802232	snp	C/G	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80272049	CAGCACTTTGAGAGG[C/G]CAAGACGGGTGGATC	57674
rs145806067	snp	A/G	1.64757e-05	0.00287012	missense	RNF213	GRCh38.p7	17:80345368	GTCATCAAGAGAGAC[A/G]TCATGACCAGGGACC	57674
rs145827743	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80306120	GGTGTGAGCCACCAC[A/G]CCTGCCCTCAAGTAG	57674
rs145828000	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80274118	GGTGCGTGTCTTGCG[C/T]TTCTGTAGGCCTCTG	57674
rs145830538	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315555	GTGATGGTGGTCGTG[A/G]AGGTGATGGTGGAGG	57674
rs145853311	snp	C/G	0.0189856	0.0955633	intron-variant	RNF213	GRCh38.p7	17:80311654	GCTGTGTTCCCCTGC[C/G]TGCTGTGGGCTTTTC	57674
rs145864827	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361239	TTTATTCCACTGGAA[A/G]AATATCCTAGGCCAG	57674
rs145888769	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80316875	GGTGTGCTATTCTTG[C/T]GACCTTTTTGAAAGT	57674
rs145888815	snp	C/G	0.0138799	0.0821421	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351467	GGGAAGAAAACGAGC[C/G]GCTAAGAGAAGATTT	57674
rs145895753	snp	C/T	0.000857053	0.0206831	synonymous-codon	RNF213	GRCh38.p7	17:80345424	GGTGCCCTTCAATGT[C/T]GACTTTGATAAACTG	57674
rs145904048	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302265	TTTTTCAAATAGCTG[G/T]AAGAGTGGAGTTTGA	57674
rs145919094	snp	C/T	0.0150606	0.0854603	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358901	TGACAGAGCAAGACT[C/T]TGTCTCAAAAAAAAA	57674
rs145947040	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB	RNF213	GRCh38.p7	17:80258844	GAGCAGCACTCCGGC[C/T]CAGCACTATTACGTG	57674
rs145951814	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310840	TACAGGCATGAGCTA[C/T]TGCACCCGGCTGATC	57674
rs145962060	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80338048	GGTGTCATCTCGTCC[A/G]TGAGGGCTGTGTACT	57674
rs145967727	snp	A/G	0.0607341	0.163335	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392038	CTCCCAAAGTGCTAG[A/G]ATTACAGGCGTGAGC	57674
rs145989142	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349519	GCAGAGACACGGGCC[A/T]CTGGGGAGGAGAGGA	57674
rs146009468	snp	C/T	9.92507e-05	0.00704383	synonymous-codon	RNF213	GRCh38.p7	17:80343145	AGGAAAGTCTCTGTA[C/T]GTGAAGAGGTTGCAC	57674
rs146021745	snp	C/T	8.314e-05	0.00644695	missense	RNF213	GRCh38.p7	17:80347049	TGTCACGTGGCAGCC[C/T]CAACGAGACAGAGCT	57674
rs146074765	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319704	TTGACAGAACATTTA[G/T]GGAAGCAAAATATGT	57674
rs146075826	snp	G/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80272712	GAGTGAGTGTGGGGC[G/T]GGCAGAGTGGGTGCT	57674
rs146084319	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80317731	CCAGAGGGCATGTTA[C/T]AGTGCTCTCTTAGCT	57674
rs146085630	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353347	GGGGCTGCCTTGGGG[A/G]CTGATCTTCATGACC	57674
rs146091300	in-del	-/GTGCATGCGTGCATGC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379043	CAGCAGGGCATGGTG[-/GTGCATGCGTGCATGC]GTGCATGCGTGTGGT	57674
rs146124849	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355598	GAATGGGGGCTTACA[-/G]GGGGAAGAAGCGGGG	57674
rs146136675	snp	A/G	3.41309e-05	0.00413089	synonymous-codon	RNF213	GRCh38.p7	17:80347263	TAGAAAGCCTTCCCC[A/G]CAAGACATTGCACAG	57674
rs146144944	snp	A/T	0.000178658	0.0094497	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389392	ACACCGAAAAGGAAA[A/T]CAGCACAGCCCCTCA	57674
rs146170558	snp	A/G	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80286026	CGCCCAGGCTGGAGT[A/G]CAGTGGCCAGATCTC	57674
rs146195097	snp	C/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80335000	AATCTCGGCTCACTG[C/G]AACCTCCACCTCCTG	57674
rs146197143	snp	A/G	0.0271762	0.113356	intron-variant	RNF213	GRCh38.p7	17:80284016	ATCACCTGAGGTCAG[A/G]AGTTCAAGACTAGCT	57674
rs146200316	snp	C/G/T	0.000362794	0.0134636	missense, synonymous-codon	RNF213	GRCh38.p7	17:80313119	AGTTTTTACAAAGAA[C/G/T]ATGCTCACATCTTCA	57674
rs146204002	snp	C/T	4.95021e-05	0.0049748	synonymous-codon	RNF213	GRCh38.p7	17:80346414	CATCGGGGTGTGTTA[C/T]CATGCCTCTTTAGAA	57674
rs146206511	snp	A/G	0.000117238	0.00765541	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363683	GCCCAGTCCCCAGGC[A/G]TGGCTACAGTTGGTG	57674
rs146206617	snp	C/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80332723	GGCTTTGAAAAGGGG[C/G]GCGGATGACTTAGAG	57674
rs146220804	snp	A/C	6.75105e-05	0.00580954	synonymous-codon	RNF213	GRCh38.p7	17:80340286	GGTCCCGAAGCAGAC[A/C]CTGTCGGCGGCAGCC	57674
rs146235437	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320315	TTGGGTATGGCTTAT[C/T]TCACTGAGCATAATG	57674
rs146238297	snp	C/T	0.000307953	0.0124049	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363301	GGAACCATGAGCTGG[C/T]TGGATGTGAGATGGT	57674
rs146256408	snp	A/C/T	0.000675725	0.018369	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367768	TCGAGAGAACTCTGA[A/C/T]GTGAAGACGCACGGG	57674
rs146290410	snp	C/T	0.0232847	0.105357	intron-variant	RNF213	GRCh38.p7	17:80270802	CTGGGTCACCGTTGC[C/T]CAAGTCCAGGCTTGA	57674
rs146299484	in-del	-/TCTT	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357330	GTAGTTAACCAATTA[-/TCTT]TCTGTCTGCCTATCT	57674
rs146312292	in-del	-/AAGAT	0.0611083	0.163768	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393754	TGAGAGATGACAATG[-/AAGAT]TAGATGAAATTGGAA	57674
rs146331063	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379522	TCTGAGGGTGCTCAC[A/G]TCTGCCGGTGATAAG	57674
rs146340028	snp	A/G	8.49264e-05	0.00651583	missense	RNF213	GRCh38.p7	17:80347189	GACAAGGAATTCTTC[A/G]GGCTTCGTGACTACT	57674
rs146342433	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376649	TGAGCATCTTTATCT[C/T]CTCAGTTCTCTGCCT	57674
rs146352280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335356	GCAGGAGGGGCACAG[A/G]TGGCAGTGCAGGTGT	57674
rs146359814	snp	A/G	3.29598e-05	0.00405941	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383905	AAAGAAAGAGTGCCC[A/G]TCCTCTGGCATTTCC	57674
rs146409979	in-del	-/T	0.0944967	0.195752	intron-variant	RNF213	GRCh38.p7	17:80305339	GTGCGCCACCACGCC[-/T]GGCTAATTTAGGATT	57674
rs146434253	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80282742	TGCTCTGTCTCCCAG[A/G]CTGGAGTGCAGTGGT	57674
rs146447798	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80308857	TTATCTTAGTCACAA[A/G]TTCAGGACTGACTGA	57674
rs146472104	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80268828	GTGTATTATGGAGAA[C/T]TGGCTCACACAATCA	57674
rs146478822	in-del	-/AGAG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359607	GAAAGAGCGAGAGAA[-/AGAG]AGAAAGAAAGTAAAG	57674
rs146486225	snp	A/G	8.2573e-05	0.00642493	missense	RNF213	GRCh38.p7	17:80346446	AGAAAGACTCATATC[A/G]GAAAGCCATCGCCAG	57674
rs146514228	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80344262	CAGGCTTCATGCTGT[A/G]TGCCCAGTCTGAATC	57674
rs146522582	snp	C/T	9.54535e-05	0.0069078	missense	RNF213	GRCh38.p7	17:80317197	TTGCAGGTCTGGAGG[C/T]GGCTGGTGGAAATCC	57674
rs146548999	snp	A/C/G	0.000164815	0.00907637	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351767	ACAAAACTGTCCCGG[A/C/G]TGGGAAGAGGAACAG	57674
rs146573135	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80271024	TCTTGCTGGTTGGCC[C/T]TTCCCTTAGTCAATC	57674
rs146608792	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357692	CAAAAAATAAAGCAG[A/G]TAAGTGCGGTGGCTC	57674
rs146610940	in-del	-/TTTG	0.0283406	0.115616	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360330	TTTTAGTTTTCACAC[-/TTTG]TTTGTGCAGTAAGCG	57674
rs146635119	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306185	GTCCCTCCAGCATTG[A/G]TTTCCTCCATTTTCC	57674
rs146644034	snp	C/T	0.00159333	0.0281803	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388572	TGGAAATGTCCACGA[C/T]GGATTTAATTTTAAA	57674
rs146664713	snp	A/G	0.153665	0.230694	intron-variant	RNF213	GRCh38.p7	17:80318865	GGCGTGAGCCACCGC[A/G]CCCGGCCTATATGTA	57674
rs146668070	snp	A/G	8.23716e-05	0.00641709	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375783	GACCCCCCAAAGCCA[A/G]CAGTCAGCCTACTTC	57674
rs146710810	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375297	CATGTGGGGCATGAC[C/T]CCAGGTGTCCAGGCC	57674
rs146716838	snp	A/G	0.0267878	0.112589	intron-variant	RNF213	GRCh38.p7	17:80290896	CTCACTGCAGCCTCC[A/G]CCTCCTGGGTTCAAG	57674
rs146729360	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80317910	AGAATGGGGTCACCC[A/G]GACACTTGAAGGATG	57674
rs146731742	snp	A/G	0.00235327	0.0342213	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372631	AAGCCGGGGCCGAGA[A/G]CCTGCCAACGAGGCC	57674
rs146746574	snp	C/T	1.65023e-05	0.00287244	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354554	TGCAACCAGGACGCT[C/T]TCCAGGAGGCGGGCA	57674
rs146754081	snp	C/T	0.00645308	0.0564349	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367856	CTCAGCAGGTGAGAC[C/T]TTAGGTTTGGATCTG	57674
rs146754687	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80316214	CTATGACTGTGCCAC[A/T]GCACTCCAACCCAGG	57674
rs146768666	in-del	-/GGT	0.442385	0.15965	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359498	CTGCACTCTAGCCTG[-/GGT]GGTGACAGAGTGAGA	57674
rs146798784	snp	C/T	0.000757501	0.0194468	synonymous-codon	RNF213	GRCh38.p7	17:80294916	CTTCTTCACCCAGTT[C/T]GAGCAGTTTTGCTTT	57674
rs146838631	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305914	GTGAGCCACCACGCC[C/T]GGCCATTAAGTTAAT	57674
rs146850239	snp	A/G	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80302133	GAGAGGCGAGGAAGG[A/G]TGGGGAGAGGGCTAG	57674
rs146850447	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80332939	TCATAGGCTCTCTCT[A/G]GGTTACAGAAGCCAA	57674
rs146853953	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388419	TGGCTGTGAGGACTC[C/T]GCTGGATTCCCGGTT	57674
rs146864156	in-del	-/GTT	0.0271762	0.113356	intron-variant	RNF213	GRCh38.p7	17:80297160	CCTTACGTTTAAAAA[-/GTT]GTTTTGGGGCCGGGC	57674
rs146866316	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384925	ATCACAGGAAATGAC[A/G]CTGACCAGATTAAGC	57674
rs146877539	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80330019	TCATCATTTTTCTCT[C/T]GGATTTTCTATCTCT	57674
rs146910347	snp	A/G	4.94662e-05	0.00497299	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361744	TGCAGGACTGCCCAA[A/G]AAGTTCGTGGACATC	57674
rs146938946	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80294438	CATAGTTAGAGATCC[A/G]TTGCAAGTCTCAGGC	57674
rs146961787	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291480	CTCCCGCCTCAGCCT[C/T]CCATGGTGTTGGGAT	57674
rs146970619	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334380	TTGGCCAAGGACTAC[A/G]TAAAGGGCAGAAAGA	57674
rs146974744	snp	A/G	1.66504e-05	0.0028853	synonymous-codon	RNF213	GRCh38.p7	17:80273326	GGAGGAAGGGGGCCC[A/G]TGCTTGTTCCCGGGC	57674
rs146976815	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389038	GCCTGCACACCGTGC[A/G]CCCAAGTGTCAGCTG	57674
rs146990608	snp	A/G	0.000280184	0.0118327	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386360	TGTGCTACCGCTCTC[A/G]TCAGCTACTTGATTC	57674
rs147013725	snp	C/T	8.28796e-05	0.00643684	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381666	TGCCGACGAGACCAT[C/T]GGCGTGGTCCACCTC	57674
rs147037632	in-del	-/AC			intron-variant	RNF213	GRCh38.p7	17:80281492	CCCCCCAACATACAT[-/AC]ACCCCACTCACACAC	57674
rs147042901	snp	C/T	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80310123	CCCCACTCACCCCCA[C/T]GTCTCTGAGCTCTGT	57674
rs147058696	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391554	CCTAAATTACCTCTT[C/T]GTATCTTTTTCTTTT	57674
rs147065656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307091	TGGCATTGTGATTCA[A/G]TCTTTTGTCCTGTTT	57674
rs147067083	snp	C/G	0.0205511	0.0992634	intron-variant	RNF213	GRCh38.p7	17:80336876	ACTGTACTCCAGCCT[C/G]AGTGACAAAGTGAGA	57674
rs147076172	snp	A/G	3.31978e-05	0.00407404	missense	RNF213	GRCh38.p7	17:80347348	CTGGCCAATTTGCCC[A/G]AGGCCAAGTGCTCAG	57674
rs147099973	snp	A/T	0.487746	0.0773096	intron-variant	RNF213	GRCh38.p7	17:80315845	TGGTGATGGTGGTGG[A/T]GGTGGTGGTGGAGGT	57674
rs147119464	snp	C/G	0.000148254	0.00860844	synonymous-codon	RNF213	GRCh38.p7	17:80309033	GATTCCCGAGGAGGC[C/G]TTGTCACCATCCTAC	57674
rs147131622	snp	C/T	0.00240507	0.0345941	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386753	TGAAGTGGAGCGGGA[C/T]CTGACTCCACTGATT	57674
rs147152819	snp	A/C/T	4.95105e-05	0.00497526	missense	RNF213	GRCh38.p7	17:80348252	AGGCACACCTGCACA[A/C/T]GGCAGACCTGGAGCG	57674
rs147181458	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80278443	GGAGGCCCGGGGCGC[C/T]GGGAGCCTGGTAGGG	57674
rs147194772	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356267	TCAGCCTCCCGAAGT[C/G]CTGGGATTCCAGGCG	57674
rs147200481	in-del	-/A	0.0626037	0.165477	intron-variant	RNF213	GRCh38.p7	17:80328684	CCAAATAACATGCTT[-/A]AAGTGTCTCCTGGAT	57674
rs147222472	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315146	GGAGGTGATGGTGGT[A/G]AAGGTGATGGTGGAG	57674
rs147250592	snp	G/T	0.00159617	0.0282053	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399026	CTCAAATGCATTCAA[G/T]CTGTAGCTGCAACTG	57674
rs147258447	snp	G/T	0.000233567	0.0108041	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373052	AACGACTGGCACCGG[G/T]TGTACCTGGTGCGGA	57674
rs147286130	in-del	-/TC/TCTC			intron-variant	RNF213	GRCh38.p7	17:80342536	CTGGGACTTAATTTT[-/TC/TCTC]TCTCTCTCTCTCTCT	57674
rs147301132	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369354	AGTGAGCGGAGATCG[C/T]GCCACTGTACTCCAG	57674
rs147309852	snp	C/T	5.49254e-05	0.0052402	synonymous-codon	RNF213	GRCh38.p7	17:80317217	GGTGGAAATCCAATT[C/T]CCCGCGGAGCATGGC	57674
rs147311375	snp	A/C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287041	AGAGGTGCATAAAAC[A/C/G]TGGAAAGCCTGTGTG	57674
rs147324380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366388	CCAGGGTCTGAATTT[C/T]TCCACATCATGGGCA	57674
rs147359815	snp	C/T	8.23621e-05	0.00641672	synonymous-codon	RNF213	GRCh38.p7	17:80290609	CACCGTGTTCTTCCA[C/T]GCCATCATCTCTCTT	57674
rs147393240	snp	C/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80304127	TGCAGTAGCATTGTT[C/G]CTAAAGATCCAATCG	57674
rs147394603	in-del	-/CTAT	0.174932	0.238463	intron-variant	RNF213	GRCh38.p7	17:80269370	ATCTGTCCACCTACC[-/CTAT]CTATCTATCTATCCA	57674
rs147408147	snp	C/T	1.64841e-05	0.00287085	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386355	GCCTCTGTGCTACCG[C/T]TCTCGTCAGCTACTT	57674
rs147411310	in-del	-/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80271157	AGGCTCAGAATCCCT[-/G]GTTGTAGGTGAAACA	57674
rs147416009	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300481	ACTCCTGACCTCAAG[G/T]GATCCACCTGCCTCG	57674
rs147425020	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80329377	GTTTCAATGTGCTGC[A/G]CCATCATTGCCTCCA	57674
rs147448930	snp	A/G	3.2962e-05	0.00405954	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369679	TGCCCAGAGTAGGTT[A/G]CTTTCTTCCTGTAAA	57674
rs147452490	snp	C/G/T	3.45873e-05	0.00415844	stop-gained, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376962	GCGAGTCCACTGGTA[C/G/T]AGTAAGTGTTGGGGT	57674
rs147458675	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367165	TTATACAACGTGGTA[C/T]CATTGATATCAAGTT	57674
rs147469449	snp	A/G	0.000411763	0.0143427	synonymous-codon	RNF213	GRCh38.p7	17:80345238	GAGGTGGGAGTCGGA[A/G]CCTCACCCATACGTT	57674
rs147479626	in-del	-/GC			intron-variant	RNF213	GRCh38.p7	17:80323835	AAGTACTTTTTTTTG[-/GC]GGGGGGGGTGCTATT	57674
rs147521107	snp	A/G	0.00260043	0.0359646	missense	RNF213	GRCh38.p7	17:80345752	GAAAATGTGGCCTTC[A/G]CCAATAAGGACCAAC	57674
rs147523333	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80263947	ATCTCAAAAGTGACC[A/C]CAGAGTCTGTTTTGG	57674
rs147532787	snp	A/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80289604	TCAGAAAAAAAAAAA[A/G]AAAAGAAAATGTGGA	57674
rs147534085	snp	A/G	0.000235306	0.0108442	missense	RNF213	GRCh38.p7	17:80298326	TCCCTTCCAGCTGGC[A/G]GCTGTACCTGGTGAA	57674
rs147553652	snp	C/T	0.00636936	0.0560724	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354779	AGGTGCTGGACTCTT[C/T]CTCTAATTTCGTGTT	57674
rs147554234	snp	A/T	0.0221141	0.102801	intron-variant	RNF213	GRCh38.p7	17:80300732	AATTTTTGTATTTTT[A/T]GTAGAGATGGGGTTT	57674
rs147557959	snp	A/C/G	0.000214365	0.010351	synonymous-codon	RNF213	GRCh38.p7	17:80347533	GGGGGACCAGCAGCC[A/C/G]GAGATTATTTTTGGT	57674
rs147563262	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80351012	GTGTTTGTAGGGGAA[A/G]TCTGATGCTCTTAGA	57674
rs147565591	snp	C/T	0.00100375	0.0223801	intron-variant	RNF213	GRCh38.p7	17:80298299	CAGCTCAGCTCACTG[C/T]GGGATCTTTATTCCC	57674
rs147581161	snp	C/T	0.000760488	0.019485	synonymous-codon	RNF213	GRCh38.p7	17:80346972	CCCCCACAAAAAGGT[C/T]GGCTTCGTGGGCATC	57674
rs147596173	snp	A/G	0.00597247	0.0543191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378150	CTAGGAAAGAAAATT[A/G]CTACTGGTTGGGAAC	57674
rs147617069	snp	A/G	3.34426e-05	0.00408903	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389352	AATGGGTGATCAGAC[A/G]ATTCACGTGTTAAAG	57674
rs147636729	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80273812	TTTAGTAGAGACGGG[A/G]TTTCACCATGTTGGT	57674
rs147664102	snp	A/G	0.0007589	0.0194647	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368136	CCAGCTGTTTCCCAA[A/G]CGCACAGGTACAACA	57674
rs147669526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311933	GGAGTTCGAGACCAG[C/T]CTGGCCAACATGGTG	57674
rs147673003	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361640	CCCATTCAACAAGGC[A/G]TCCCCATTCCCCTTC	57674
rs147702922	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80337010	CCTGGGCCAGCCTCC[A/G]GACGGCTGCTCTGCA	57674
rs147705361	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391627	ACAGGGGTTCATCTT[C/G]TCTGCCGTGTGCCAC	57674
rs147741247	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80284715	GCCTTCCGGACGGCT[C/T]CCCCACTGAGCCTCT	57674
rs147762057	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80326159	AGGTCTTCTCTGTTG[C/T]GCAAGTTAGCATGTA	57674
rs147785564	snp	A/G	0.00511052	0.0502906	missense	RNF213	GRCh38.p7	17:80349770	TTCTTAACTCTGTAG[A/G]TCACCACTTTCTCCA	57674
rs147786232	snp	A/C	1.66427e-05	0.00288462	missense	RNF213	GRCh38.p7	17:80273304	TGGAGTGTGGGCAGG[A/C]GCTGAAGGAGGAAGG	57674
rs147834926	snp	C/T	0.00158084	0.02807	synonymous-codon	RNF213	GRCh38.p7	17:80347707	CTACGTCCACCTCGG[C/T]GGCCAGAAGTACGTG	57674
rs147868237	snp	A/C/T	0.00902064	0.0665617	missense	RNF213	GRCh38.p7	17:80339481	ACCTGAACTTCTACA[A/C/T]GGCAGAGCAGCTGGT	57674
rs147869268	snp	A/G	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287380	TAGTGATGCTCACCT[A/G]TAGTCTCAGCTACTC	57674
rs147876946	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80336758	AAACATTTAAAATTA[G/T]CCAGGCATGGTGGTG	57674
rs147879460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284935	GCCAGGATGATAGAC[A/G]TCAGTGGTTGACACC	57674
rs147895486	snp	A/G	6.81861e-05	0.00583853	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373147	GTGGGTGTTTCCCAA[A/G]GACGTTGTCAAGCAG	57674
rs147895650	snp	A/G	0.000148281	0.00860922	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319339	CTCCTCCTGGGAAAC[A/G]GATTCGGGCTCACAG	57674
rs147900479	snp	A/G	0.00422873	0.0457874	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364503	GGAACCGAGAGCCGC[A/G]TCCCCGAGTTACAGG	57674
rs147910217	snp	A/G	0.00342815	0.0412592	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361924	TAAGGGTCAGGTGTA[A/G]AGCTTGCATGATGGG	57674
rs147941497	snp	C/T	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369530	AAGCATGCCCGCTTC[C/T]GGCAGATGTGCAACA	57674
rs147971398	snp	A/G	0.000214166	0.0103459	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288645	CAGGCAGTTGATGCT[A/G]TAGCTGAGCCAGCCA	57674
rs147977147	snp	C/T	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393035	CAGGCTGGAGTGCAG[C/T]TGTGCAATCTCAGCT	57674
rs147981155	snp	C/T	8.25076e-05	0.00642238	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363148	GGAAACTGAAAGCGG[C/T]GTCAGAAGCGCCCGA	57674
rs148025676	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80285557	GCTTCCCCCTCTCAG[C/T]AGGTCCCCCGGCAGC	57674
rs148067887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310454	GACAGGGTTTCACCA[C/T]GTTGGCCAAGCTGGT	57674
rs148072359	snp	C/T	0.00795532	0.062565	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359815	AGATTTTGGGCAACA[C/T]ACTTGACCCCTGTCA	57674
rs148087648	snp	C/T	0.000445056	0.0149107	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386398	CAATGAAATTGTCTA[C/T]GCCGTGGAAAAACTC	57674
rs148089096	snp	C/T	2.70018e-05	0.00367426	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287859	GAAGGGGAACAAGTC[C/T]GCTTCCTCAGAGCTG	57674
rs148111185	snp	G/T	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80328267	CGCTTTCAAAGCATT[G/T]CCATGGAAAATGGCA	57674
rs148121364	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356191	ATTTTTAGTAGAGGC[A/G]AGATTTCACCATGTT	57674
rs148136053	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365720	GAGGATAGTAGGACA[C/G]AGCCGGTGCCCCCCT	57674
rs148139681	snp	A/C/T	0.000701917	0.0187229	synonymous-codon, missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353526	GTGGGCTTGGAACAC[A/C/T]GGGCGGAAGACGGCC	57674
rs148140383	snp	C/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80295445	TCTCACAGGTGTGGT[C/G]GTGGGGCACGGAATG	57674
rs148143253	snp	A/G	0.00086865	0.0208224	missense	RNF213	GRCh38.p7	17:80289744	AGCCTGAAGACCTCA[A/G]GAAGCCAGAGGGGAA	57674
rs148156651	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378794	TTGGTGTGTTATCAG[C/T]CGTGACTCTCAGTAT	57674
rs148157068	snp	A/G/T	0.00129076	0.0253777	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371944	GCATTCATAACTGAA[A/G/T]ATAAAACTGAACTGT	57674
rs148165261	snp	C/T	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80323561	TGTTAGACAGAGTCT[C/T]GCCCTGTTGCCCAAG	57674
rs148194596	snp	G/T	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80291402	TTGCTCTGTCACCCA[G/T]GCTGGAGTGCAGTGG	57674
rs148213205	snp	A/G	0.00023062	0.0107358	missense	RNF213	GRCh38.p7	17:80345648	TTAGCGACCTGCGGC[A/G]TGGTGGTACCAATGC	57674
rs148238829	snp	A/G	0.0228947	0.104514	intron-variant	RNF213	GRCh38.p7	17:80261813	CACCTGAGGTCGGGA[A/G]TTCGAGACCAGCCTG	57674
rs148253055	in-del	-/G	0.115788	0.21092	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387295	TTTTTTGGTAGAGAT[-/G]GGGGCTTCACCACGT	57674
rs148282853	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389620	TGAGGCCCCTGCAAA[C/G]AGCGTGATGTGAGCG	57674
rs148300588	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80275145	GAGTGGTGTGTGTGT[G/T]TTGGGAGTGTGTGTG	57674
rs148301460	snp	C/T	1.66319e-05	0.00288369	missense	RNF213	GRCh38.p7	17:80347130	GAGTCCAAGGGTACT[C/T]TGCGTCCTTTGCCAA	57674
rs148323082	snp	A/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80303489	ACTTCTGCTAAAGGC[A/G]GTGTTACGGTCTTGC	57674
rs148337328	snp	C/T	0.00755907	0.0610114	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385977	AGCCAGCACTGTTAA[C/T]GCTTAACTTGTGTCT	57674
rs148347347	snp	A/G	0.029116	0.117091	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398461	AAGATAGACTGGCCA[A/G]CATTAGAGGTAGGTT	57674
rs148356224	snp	A/G	0.0171505	0.0910007	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319345	CTGGGAAACGGATTC[A/G]GGCTCACAGCTGTGT	57674
rs148369056	snp	A/G	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80343985	CCTGGAAAGGAGGAC[A/G]TCAGTGCCGTCGAGG	57674
rs148408469	snp	A/G	1.65061e-05	0.00287277	missense	RNF213	GRCh38.p7	17:80347429	CAGAAGGTGCCGGGT[A/G]GAGAGCAGGAAGATG	57674
rs148418226	snp	C/T	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80305700	CACTGCAATCTCTGC[C/T]GCCGGGGCTCAAGTG	57674
rs148421129	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355684	TACAGGGGGAAGAAG[C/T]GGGGTGACCGGGAAT	57674
rs148431622	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387486	CCTCCATGGGTAACC[C/T]GCCAGCAGATGCCAT	57674
rs148461738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272884	ACAGGAGGAATGTCT[A/G]CAGTAGGGGAGGAAA	57674
rs148504719	snp	A/C	0.0103295	0.0711199	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371064	TTACAAGACCTGCAC[A/C]GCCCAGTGAACCAAT	57674
rs148511638	snp	A/G	0.0166325	0.0896639	intron-variant	RNF213	GRCh38.p7	17:80317581	TTTACTTGGCCCGCC[A/G]TGCTCAACCCCTTGT	57674
rs148541222	snp	A/G	0.000197655	0.00993922	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377788	GGCCATCCTTGCTCC[A/G]TGGGAGAGGTGAGTC	57674
rs148590969	in-del	-/T	0.197543	0.244435	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351665	TTAAAATAGGTATTC[-/T]TTTTTTTTTCTTTAA	57674
rs148593553	snp	C/T	0.000106595	0.00729972	missense	RNF213	GRCh38.p7	17:80289777	ACAGAAGTGCAGCTG[C/T]TGTGAAAAACGAGAA	57674
rs148610110	snp	C/T	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80313079	TCCAAGGGACCCTTG[C/T]TGCTACGAAAAGGTG	57674
rs148613334	snp	A/G	0.000484287	0.0155534	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288135	GGCTCAGAGCAGCCC[A/G]CAATTCCAGGACCAC	57674
rs148615211	snp	C/T	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388664	ATGAACATCTCTTTA[C/T]GGACATCAAGAACAA	57674
rs148626399	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329754	GAGGATCACTTGAGC[C/G]TGGGAAGTCGAGGCT	57674
rs148636555	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259001	TCATTTAAACATTTC[A/G]ACTAGTCATACTGAA	57674
rs148647030	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286891	CGCAGTCCTGGTTCC[A/G]AAATGGGGACCGTAC	57674
rs148650123	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338261	GAACGCTGAAGCTGG[C/T]AGCCTGTCCACCGCA	57674
rs148653181	snp	A/G	0.000465673	0.0152519	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354076	CAGAGCGCCGTGGGC[A/G]TGCTCAGAGACCAGA	57674
rs148663578	snp	C/G/T	8.25539e-05	0.00642418	missense, synonymous-codon	RNF213	GRCh38.p7	17:80343160	CGTGAAGAGGTTGCA[C/G/T]GACAAAATGAAGATG	57674
rs148668623	snp	A/G	0.0670745	0.170406	intron-variant	RNF213	GRCh38.p7	17:80297712	GAATGGCGTGAACCC[A/G]AGAGGCAGAGCTTGC	57674
rs148682884	snp	A/G	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380205	TCCAGGTACAAATCC[A/G]ATCCCACAATCCCAT	57674
rs148687848	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307922	ATTTGGGTTTATCTC[C/T]CCCTGATCTTTTTTC	57674
rs148712925	snp	A/G	1.64773e-05	0.00287026	missense	RNF213	GRCh38.p7	17:80346281	GTGTGAAAGTTTTCA[A/G]GTGGTTCCACGAGCA	57674
rs148722269	snp	A/G	0.0333695	0.124785	intron-variant	RNF213	GRCh38.p7	17:80293143	GCTCACTACAGCCTC[A/G]ACCACCAGGGCTCAG	57674
rs148731719	snp	A/G	0.0185063	0.0943964	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376310	TGTCAGCAATGTGAA[A/G]CTGTGAGCAAATTCA	57674
rs148753389	snp	C/T	6.59087e-05	0.00574021	missense	RNF213	GRCh38.p7	17:80345990	TTAGTATGGAGGAGA[C/T]GGCCGACAGGCTGGG	57674
rs148775294	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80342419	TGAAGGTTCAAGAGC[A/G]TATTCTTGAATCTGA	57674
rs148776624	snp	A/C/G	0.00189261	0.0307038	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383801	CCCACCTGCCCCGGA[A/C/G]AAGTGTGGTCCATTG	57674
rs148805834	snp	C/T	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80267891	GTGGCTGGTCCTCAG[C/T]TCACTGCAACCTCCG	57674
rs148818590	snp	C/G	1.65734e-05	0.00287862	missense	RNF213	GRCh38.p7	17:80347071	GACAGAGCTCATAGA[C/G]AGCGCCAAGGGCATC	57674
rs148914205	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80316233	CTCCAACCCAGGTGA[C/T]GGAGCGAGACCCTGT	57674
rs148915284	snp	A/C	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80269314	CCAATCAAATTGACA[A/C]CTGATATTAACCATC	57674
rs148915446	snp	C/T	1.65822e-05	0.00287938	stop-gained	RNF213	GRCh38.p7	17:80347114	ATCCTCGTCCAGGAC[C/T]GAGTCCAAGGGTACT	57674
rs148918801	snp	A/C/G	0.000118186	0.00768646	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363716	GAATCTTTCCATGCC[A/C/G]CTGGAGCTCATCTGC	57674
rs148946177	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355839	AGAAGAAGCGGGGTG[A/G]ACGGGAATGGGGACT	57674
rs148958011	snp	C/T	0.000972386	0.0220283	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364505	AACCGAGAGCCGCGT[C/T]CCCGAGTTACAGGGG	57674
rs148968472	snp	A/G	8.23798e-05	0.00641741	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369554	TGCAACAGTTTCTTC[A/G]TAGACCTGGTGTCCA	57674
rs148974884	snp	A/C	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80322840	TATGTGTTGTTTTTT[A/C]ACATTCTTATTGGTT	57674
rs148984748	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80274108	GCGTCCGCTGGGTGC[A/G]TGTCTTGCGCTTCTG	57674
rs148995852	snp	A/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80282248	GTTGCTACACGGTGC[A/G]GTGTTGCTCTTTGTG	57674
rs148999614	snp	A/G	0.0166325	0.0896639	intron-variant	RNF213	GRCh38.p7	17:80333153	TCCCAGGTTCACGCC[A/G]TTCTCCTGTCTCAGC	57674
rs149068066	in-del	-/CTGAGTCCCTC			intron-variant	RNF213	GRCh38.p7	17:80308460	CTCCTAAGCCTCCTT[-/CTGAGTCCCTC]CTGAGTCCCTCCTAA	57674
rs149072554	snp	A/C/T	1.64931e-05	0.00287163	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380947	TTATCCGGCTACTCA[A/C/T]TCACTTGGCTCTGCT	57674
rs149124360	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80291090	GTGCTGGGATTACAG[G/T]CATGAGCCACTGCGC	57674
rs149136204	snp	C/T	3.29489e-05	0.00405874	missense	RNF213	GRCh38.p7	17:80319280	AAGACCTTCGAGAAA[C/T]GCATCATTGAAGCCG	57674
rs149154359	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80261535	CTGTGCAAACATGGT[A/G]GTGGCCCTTCCCTGC	57674
rs149177904	snp	A/C/T	0.0040976	0.0450778	missense, synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287950	CCTCAGGACACAGCC[A/C/T]TGCCCCACAGCCAAG	57674
rs149179590	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315220	AGGTGATGGTGGTGG[A/T]GGTGGTGGAGGTACT	57674
rs149186984	snp	A/G	0.176219	0.238865	intron-variant	RNF213	GRCh38.p7	17:80298894	TGAGGTAGGAGAATC[A/G]CTAGAACCCGGGAGG	57674
rs149200340	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381892	ACCGTGTCTAGGGAA[A/G]GCGATGCCTGGGGCT	57674
rs149206366	snp	A/C	0.000115554	0.00760025	intron-variant	RNF213	GRCh38.p7	17:80309223	ATAGGTGCGGAATTT[A/C]AAGCAGCCTCAATTT	57674
rs149228852	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80336684	GTTGTAATTGTCATT[C/T]TATTCTGTTACTTTT	57674
rs149230960	snp	C/T	9.88533e-05	0.00702971	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375772	CAGGCCTGCAAGACC[C/T]CCCAAAGCCAGCAGT	57674
rs149232232	snp	C/T	8.27712e-05	0.00643263	synonymous-codon	RNF213	GRCh38.p7	17:80340214	CCAGCACAAGGTCTT[C/T]GTCACCCCCCAGGCA	57674
rs149264311	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80263380	GCATCCCCTATCCCC[A/C]CCCAGCCCAACCCAT	57674
rs149271365	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80342174	GCCCCCATGCTGTCA[C/T]GGCTTGCAGCCCAGG	57674
rs149274020	snp	C/T	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80289019	GCCCGAGTGGCCGGG[C/T]GAGGCCTCTCTTAGG	57674
rs149295002	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315387	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs149316372	snp	C/T	0.0185938	0.0946107	intron-variant	RNF213	GRCh38.p7	17:80310338	GCTCACTGCAATCTC[C/T]GCCTCCTAGGTTCAA	57674
rs149326553	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80337561	CTCCAACCGTGGCCC[A/G]TGTTCTCTCCTTTTG	57674
rs149328179	in-del	-/AA	0.0225045	0.103662	intron-variant	RNF213	GRCh38.p7	17:80276607	GTGAGATCCTTCCTC[-/AA]AGAGAGAGAGAGAGA	57674
rs149329843	snp	C/T	0.0115144	0.0749975	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392848	ACCTGCCTCAGCCTC[C/T]CAAAGTGCTAGGATT	57674
rs149347968	snp	C/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80348764	ATGGGGAAGAATGGC[C/T]GGGAAGGGATTGTAG	57674
rs149370548	snp	A/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80306976	ATCTGTAAAAGAGGT[A/G]AGATTAGTATGTGAG	57674
rs149372744	snp	A/G	1.65064e-05	0.00287279	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352999	CTCATGGTTTCTGAT[A/G]TGACCAGGCTGCAGC	57674
rs149388081	snp	A/G	3.33389e-05	0.00408269	missense	RNF213	GRCh38.p7	17:80346538	GATCTTTTTCTGGAC[A/G]GCGTACCTCTGAGGA	57674
rs149441718	snp	C/G	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80270764	ACCCAGCTCTCCTAG[C/G]CTTGCTCAGCAAGAG	57674
rs149449382	snp	A/C/G	0.000263923	0.0114848	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364530	CAGGGGCTGGTGACC[A/C/G]AGCACGTCTTCTTAC	57674
rs149475943	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286409	TGGCCATGTGTGATA[A/G]AGAAGGGGTTGCAGT	57674
rs149502065	in-del	-/TTTA	0.202343	0.245416	intron-variant	RNF213	GRCh38.p7	17:80299535	TATTACCAGAGAAAG[-/TTTA]TTTATTTATTTATTT	57674
rs149502902	snp	A/G	0.000146071	0.00854482	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372979	TGGCCTCTCAGAGAT[A/G]GCCAAGGAGAAGCAG	57674
rs149509354	snp	A/G	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80325534	TGGAGAAGGCAATGC[A/G]ACTTACCTAAGGTCT	57674
rs149527973	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80334514	GCCACTTCGGAAGCT[A/G]TAAATGGCTCAGGTT	57674
rs149529286	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80283692	GAAAGAAGCGGTAGG[G/T]GGCCTGCATCTTCCA	57674
rs149537867	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362750	GTCCTTTTCAGCTTT[A/G]CTTCGAAAAATAAGA	57674
rs149560351	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376188	CCTCAAATGGTGGTG[A/G]TTTCTCCATATTTAC	57674
rs149619342	snp	A/T	0.000845385	0.0205421	missense	RNF213	GRCh38.p7	17:80295616	ATTGCCGGACGGAAA[A/T]AGCACGGACTTTTTG	57674
rs149636223	snp	C/G	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80309063	CCTGACTGTGTGTCT[C/G]AAACTGCATGAAGCC	57674
rs149643495	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80292886	ACCAGGGCCTCCCTG[C/T]CCCCTGGTGTCCGGT	57674
rs149653984	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377681	GGTCAGGGCCAGAGA[A/G]TAGAGAGTTAGCTTT	57674
rs149665301	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80305457	TGCTGGGATTACAGA[C/T]GTGAGCCACTGCGCC	57674
rs149676075	snp	C/T	0.000798403	0.0199641	missense	RNF213	GRCh38.p7	17:80332432	TTGTGAATAAATACA[C/T]GGACCTGGATTCAGA	57674
rs149678213	snp	G/T	0.0115144	0.0749975	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387139	TTGAGGTCTTTTTTT[G/T]AAACAGGGTCTCACT	57674
rs149686155	snp	A/C/T	8.2549e-05	0.00642406	synonymous-codon, missense	RNF213	GRCh38.p7	17:80298427	ATGGAGCTGGCCCCG[A/C/T]GGCACAAGGATGCCT	57674
rs149694183	snp	C/T	8.42056e-05	0.00648812	synonymous-codon, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385620	ATCGCTTGAGACGAA[C/T]GGTTAGTATCCTGTC	57674
rs149718951	snp	C/T	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80300338	GGTGTGATCTCAGCT[C/T]ACTGCAGCCTCTGCC	57674
rs149749020	snp	A/C/G	5.00499e-05	0.00500229	missense	RNF213	GRCh38.p7	17:80346613	ATGGTCGTCTGCATC[A/C/G]AGCTGAAGATTCCCC	57674
rs149801680	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80272838	TTGAGACCCCTGGGC[C/T]GCCACTGGGAGAATG	57674
rs149823675	snp	A/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80281926	CAATGGCGTGATCTC[A/G]GCTCCCTGCAACCTC	57674
rs149832829	snp	C/T	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361106	TGCTGTGACCTGTAG[C/T]CATGCAACATACAAT	57674
rs149833449	snp	G/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80311431	TGGATTGTTCTAGAA[G/T]GAGCTGTGCCATTGG	57674
rs149835146	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384741	CTCCGTACCCAGCCA[A/G]TTACATGGGCCCAAG	57674
rs149856450	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394983	TCTTCAACTTGCACT[C/T]GGAGCTCCTTTGATA	57674
rs149867798	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80350098	TGTCTGGCCTAACAT[C/T]CTCCTCCGAGAGCAC	57674
rs149877683	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80279072	GGCTGTGAAAGAGCA[A/G]CGCTGATTCAGGCTT	57674
rs149879581	in-del	-/A	0.200492	0.245049	intron-variant	RNF213	GRCh38.p7	17:80304659	AATAAATAAATAAAT[-/A]TAATAATAATAATAA	57674
rs149885418	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357448	CTCAGATCTAGTGTA[C/T]AAAAACATCAACAGG	57674
rs149899560	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353608	TGGCAGAGGAGGCCA[C/T]GGAAACAGAAAGTTC	57674
rs149905620	snp	A/G	8.45788e-05	0.00650248	missense	RNF213	GRCh38.p7	17:80346955	ATTGAAGACGATCCC[A/G]CCCCCCACAAAAAGG	57674
rs149915714	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80291643	AGACTTGGGTCATGA[C/T]CGCGTTCTTGTTGAA	57674
rs149936436	in-del	-/T	0.353371	0.227628	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396724	CGCCAGGAAAGTGCA[-/T]TTTCCCCCCCACCCC	57674
rs149963544	snp	C/T	0.0170251	0.090679	intron-variant	RNF213	GRCh38.p7	17:80318328	TCAGGCTTTTCGGCT[C/T]GAAGGTGGGGTTTTG	57674
rs149974667	snp	C/T	1.64787e-05	0.00287038	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368073	TGGTTTGCCTCAGAG[C/T]AGATGATATGCCCCT	57674
rs149993081	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287480	GCACTCCATCCTGGG[C/T]GACAGAGGGAGACCT	57674
rs150014425	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367649	ACCCCACACACACGG[C/T]GCAGCCTTGGCCCTG	57674
rs150052678	snp	C/T	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80284684	TGGTGCAGGCGTCTC[C/T]GGCCCTGTCTACTCT	57674
rs150065746	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364262	CTGAGCGTCTGAGAG[C/T]GAGAGCTGGGGGCGG	57674
rs150071649	snp	A/C/G	0.000422814	0.0145339	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288070	GAGGTTGGCGACAGC[A/C/G]CCCTGCAGGCCCAGG	57674
rs150094902	snp	C/T	0.00398564	0.0444627	intron-variant, missense	RNF213	GRCh38.p7	17:80288901	TCGGGGTGCTCACAT[C/T]CCAGCGGAGAGAGAG	57674
rs150095282	snp	C/T	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372620	TATTCTCCAGCAAGC[C/T]GGGGCCGAGAGCCTG	57674
rs150096620	snp	A/G	0.000115307	0.00759211	missense	RNF213	GRCh38.p7	17:80346173	ATGAAAACGGGACTC[A/G]CGTGATCACAGAAGT	57674
rs150107779	snp	C/G	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368730	GAGTGACCACACCTG[C/G]CCGACGCCACTGGTT	57674
rs150119350	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298655	CACGCTCTTTTAACA[C/T]TTTAAGACATCAAAA	57674
rs150148627	snp	A/G	0.00115245	0.023977	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376365	CTCCTGATATCAGCC[A/G]TTTTGCAACATCGCT	57674
rs150149915	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269026	TTTCCAAAGGCCAAA[G/T]AACCTGAAGTGTGAT	57674
rs150153160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337125	CAAAACCCTCTGTTG[C/T]GATTTTTCCTAAACT	57674
rs150162964	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365198	CACGTGAGCACATCC[A/G]GAGCCCTCACCGCCA	57674
rs150172555	snp	C/T	4.94189e-05	0.00497062	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389883	GGCAGTTCCTGTCTG[C/T]TCATAAGTCTGAACA	57674
rs150183191	snp	A/C	0.0670745	0.170406	intron-variant	RNF213	GRCh38.p7	17:80306666	ACCATCCTGGCTAAC[A/C]CAGTGAAACCCCGTC	57674
rs150183747	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379232	CCAAATGAATATAAG[A/G]AAGTCAGTTTGGAAG	57674
rs150190113	in-del	-/TTT	0.179744	0.239925	intron-variant	RNF213	GRCh38.p7	17:80300900	TGAGTGATGTTGAGC[-/TTT]TTTTCATATGCCTGT	57674
rs150203726	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388776	CTACTCCAGCCTTGC[C/T]CCGGGTGTTTGCTGT	57674
rs150268023	snp	C/G/T	0.000131953	0.00812161	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319414	GGGTCTCAGCTCCTC[C/G/T]GCTAACTCAGAGATT	57674
rs150324255	snp	C/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80274094	GGGCAGGGACCTGAG[C/T]GTCCGCTGGGTGCGT	57674
rs150339708	snp	G/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80283393	AGAGGTTCTGGGATG[G/T]CGGCTTGAGGGCAGT	57674
rs150357089	snp	A/C/G	0.00107033	0.0231091	synonymous-codon	RNF213	GRCh38.p7	17:80345670	TACCAATGCTGACAC[A/C/G]ATAAAGCTGGTCAAG	57674
rs150360192	snp	C/T	0.0146672	0.084371	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362227	CAGGGTAAGAATAAA[C/T]AAGTGAAATTCAATA	57674
rs150370233	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397335	AGTGCTCTTAAGGGA[A/G]GAGACCACCCCACAT	57674
rs150377862	snp	G/T	0.0217236	0.101931	intron-variant	RNF213	GRCh38.p7	17:80271365	CTGAGTACTCAAAGG[G/T]AAAAAGGTCTGCGTG	57674
rs150377982	snp	C/T	1.64838e-05	0.00287083	synonymous-codon	RNF213	GRCh38.p7	17:80347767	ATGTCGGGTTCACCC[C/T]AACTTCCGCCTGATT	57674
rs150390257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330819	TTGGTGTGCTGGATG[A/G]ACCATGTCTTTTTTT	57674
rs150413172	snp	A/G	0.00154723	0.0277708	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358253	CACTCTGGTTCCTCT[A/G]ACCCGTGGTGGCCCA	57674
rs150427088	snp	A/T	0.000135582	0.0082324	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360148	CCCTTTCAGCTGGAA[A/T]ATCAAGGACTATCTG	57674
rs150430703	snp	A/G	1.65457e-05	0.00287621	missense	RNF213	GRCh38.p7	17:80294990	GGACCGATTTGCAGT[A/G]CAGGGAGAAAGAGGT	57674
rs150445949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327392	GTGTTCCTAGCTACT[C/T]GGGAGGCTGAGGCAG	57674
rs150477925	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375652	AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC	57674
rs150506437	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263096	CCTTGGTCTGGTTTG[A/C]TGCCATCCACCGCAG	57674
rs150512716	snp	A/G	0.0138799	0.0821421	intron-variant, synonymous-codon	RNF213, LOC100294362	GRCh38.p7	17:80360365	CCAATTTACGTCACC[A/G]CGTCATTTTAAAGTT	57674
rs150523106	snp	A/G	0.000148311	0.00861007	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363182	AGAGGTTTCCTTACC[A/G]TGGGTGCACCTTGCC	57674
rs150540163	snp	C/T	8.26043e-05	0.00642615	synonymous-codon	RNF213	GRCh38.p7	17:80298399	GGGCGCCCTGCCTGT[C/T]CTGCACTGCTGTATG	57674
rs150554775	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328810	CCACCTCCTGTTGCT[C/T]CCTGTTTTCTCATAA	57674
rs150637306	snp	A/G	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80299890	CCTGCAAAGGACATG[A/G]TTTCATTCTTTTTTA	57674
rs150640339	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372127	AGGTTTCAAAGACGC[A/G]GCTTCTGCCTTCAGC	57674
rs150645206	snp	C/T	0.000115463	0.00759725	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386708	TTCCGTGGATGCCGC[C/T]GAGGTCACTGAACTG	57674
rs150660510	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80311250	ACAAAGCAAAAATAC[A/G]TGACGCATGTTGAAG	57674
rs150668463	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394607	TTGATATGTTAGAGG[C/T]AGTATCCTTAATATT	57674
rs150673718	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80270638	TTTGGAAGTTAAGAG[A/C]CCACATGTATGTGTA	57674
rs150696523	snp	C/T	0.0387552	0.1337	intron-variant	RNF213	GRCh38.p7	17:80296166	CAGGGACTACAGGTG[C/T]ACACTACCACACATG	57674
rs150706422	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308336	GAGTCCTTTCTTACA[A/C/T]CGCCTTCCCAGTCCC	57674
rs150709164	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356693	GGCTCCCGCCTCTCC[C/T]AGCGCTTGTCCCAGC	57674
rs150719698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389640	TGATGTGAGCGGGCT[A/G]TGAGGTGCCGCAGGA	57674
rs150726340	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80266717	ATGTTGGCCAGGTTG[A/G]TATCAAACTCCTGAC	57674
rs150749971	snp	C/T	3.33606e-05	0.00408401	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353560	AGGAGGCGATGGAGA[C/T]GGAGGCCAGCACATC	57674
rs150801820	snp	A/G	0.000802522	0.0200154	intron-variant, missense	RNF213	GRCh38.p7	17:80278896	GCCAGCGTGCCTTCT[A/G]CAGACTGTGAGCAGG	57674
rs150847252	snp	A/G	0.0413566	0.137724	intron-variant	RNF213	GRCh38.p7	17:80325244	CTCAGGCAAGGTGGT[A/G]TCTTCCTGATTGGGA	57674
rs150849968	snp	C/T	0.00131852	0.0256422	synonymous-codon	RNF213	GRCh38.p7	17:80346375	CACCGAGAGAGATCC[C/T]GTCCTCTGGTCGTTG	57674
rs150856047	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80275644	ACAGAGACTGAGAGA[A/G]TATTATTTTTTCTTT	57674
rs150864655	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80284437	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	57674
rs150900021	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319567	ATCACGGCCGTGCGC[A/G]TGTGGCACAAGTCAC	57674
rs150901669	snp	G/T	0.00716694	0.0594315	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398797	AAAAAGAAAAAAAGA[G/T]ATATATATACAAGTA	57674
rs150908874	snp	C/G	1.65081e-05	0.00287293	synonymous-codon	RNF213	GRCh38.p7	17:80348151	GGTCCGGCTGAGCGC[C/G]TACTCGCTGGGCGGG	57674
rs150952793	in-del	-/TA	0.0748431	0.178382	intron-variant	RNF213	GRCh38.p7	17:80269523	TCTATCCATCCATCC[-/TA]TCTTTCTATTCATCC	57674
rs150960261	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355709	GGGAATGGGGGCTTA[C/G]AGAGGAAGAAGCGGG	57674
rs150980347	snp	C/T	0.000197664	0.00993947	missense	RNF213	GRCh38.p7	17:80349843	TCACAGGCAGGGCTC[C/T]GAAACCCACACTCCT	57674
rs150990267	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364815	CAGAAAGGGGCTGAC[A/G]CAGGGAACATGCTTG	57674
rs150994446	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80293650	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	57674
rs150996304	snp	A/G	1.69415e-05	0.00291041	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288236	CCCCCACCTCTGCTG[A/G]TGAAGGCCATTCTAG	57674
rs151004484	snp	A/C	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320534	TAATTGTTTAAAGAA[A/C]AATGTGCCGCCACAC	57674
rs151007531	snp	C/T	0.00874735	0.0655527	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377040	ATGAAGCATTGGGTT[C/T]GACTTGGGGTCCACG	57674
rs151024579	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80264793	CCCTTACGGTGGCCA[C/T]GAGGTCCTACATAGA	57674
rs151033150	snp	C/T	1.64914e-05	0.00287149	missense	RNF213	GRCh38.p7	17:80306430	CTTTCAGGGATTTAC[C/T]ACCGGCTTCCGGGAC	57674
rs151048031	snp	C/T	0.000889152	0.0210662	missense	RNF213	GRCh38.p7	17:80290581	CCAGCACGCTGAGCC[C/T]GGGTGGAGGAGTCAC	57674
rs151050026	snp	A/G	0.000131785	0.00811635	missense	RNF213	GRCh38.p7	17:80345326	ATCAACGGCAGTGTC[A/G]ATGCCATCAGTCACT	57674
rs151055851	snp	A/G	0.000290377	0.0120459	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363749	CGATGAGCACATGCA[A/G]GGCAGCGGGAGCCTG	57674
rs151078521	snp	C/T	0.0252325	0.109451	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259270	GTCAGGAGTTTGAGA[C/T]CACCCTGGCCAACAT	57674
rs151081121	snp	C/T	0.0763149	0.179815	intron-variant	RNF213	GRCh38.p7	17:80329763	TTGAGCCTGGGAAGT[C/T]GAGGCTGCAGTGAGC	57674
rs151100315	snp	C/T	0.000296545	0.0121731	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379663	GCATTGACTGCCATG[C/T]GCCGATTGGAGGCAT	57674
rs151112444	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80281278	CACACCACTCACACT[-/C]CCCCCCCACACACAT	57674
rs151136922	snp	A/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389230	CTGCAGTCCTACAGC[A/G]ATGCCTGTGAAGTGC	57674
rs151153227	snp	C/T	6.60949e-05	0.00574831	synonymous-codon	RNF213	GRCh38.p7	17:80346846	GGACCTGCAGCAGTA[C/T]GTCTCTGTGGTGGTG	57674
rs151163115	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301578	TAGGGAAATGCAAAT[C/G]AAAACCACAATGAGA	57674
rs151171129	in-del	-/CCCC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381814	GGGCCACCCCACACA[-/CCCC]CAGCCAGTCTGAGCT	57674
rs151191387	snp	A/G/T	0.000839796	0.0204744	synonymous-codon	RNF213	GRCh38.p7	17:80294841	GCAGATTGCCGCTGC[A/G/T]CTCATGCTGGACAGC	57674
rs151196563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341354	CTTGACCCACCCTTC[A/G]TTTGCCATCTTGTTT	57674
rs151199658	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397004	CTTACTATAAGGGTC[C/T]TACCTTCCCCAGTAT	57674
rs151206421	snp	A/G	0.0217236	0.101931	intron-variant	RNF213	GRCh38.p7	17:80271272	GTCTTATGTATGTAG[A/G]CGTTTAGAGGATTTG	57674
rs151216618	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80298020	GGCCTGGGTTCAAAC[C/T]CCAGCTCTGTCAGTC	57674
rs151231231	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380744	ACTCTCTTCTCAGCC[A/G]TAAGCCTCACTCCAA	57674
rs151239822	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80309917	CCTGCCACCACGCCT[A/G]GCTAATTTTTGTATT	57674
rs151242116	snp	A/C	1.6528e-05	0.00287467	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360067	TTATTGCAGACATAA[A/C]GGTGAGATGGCCTAC	57674
rs151254584	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390923	AAAAATTAGCCAGGC[A/G]TGGTGGTACACACCT	57674
rs151260360	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80268216	TTGGTGGATTCCATA[C/T]CTTGGCTATTGTGAA	57674
rs151274876	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80333055	AGGTGACTCTTTTGC[-/T]TTTTTTTTTTTTGAG	57674
rs151313116	snp	C/T	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80346008	CCGACAGGCTGGGCT[C/T]CATTCCTCTGAGGCA	57674
rs151318745	in-del	-/TC			intron-variant	RNF213	GRCh38.p7	17:80273612	CTGGGGCCTCCACCG[-/TC]TTTTTTTTTTTTTTT	57674
rs151335315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358039	CCCTTCCAGTAACCT[A/G]ATGACAGTTTATTAG	57674
rs180714753	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269747	TTATCTATCCATCCC[A/G]TCTTATCTATCCATC	57674
rs180771491	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313737	GTGGTGGAGGTGACA[A/G]TGGTGATGCTGGTGG	57674
rs180781475	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355609	TTACAGGGGAAGAAG[C/T]GGGGTGAGTGGGAAT	57674
rs180795827	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385347	CATATTAGAAGCTTT[C/G]GCCACAGCTGAAAAG	57674
rs180810620	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367688	GCTCCCTCTGTCGCC[C/T]GGCCTGGCCGCCCTC	57674
rs180815319	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80304589	AGCTTGCAGTGAGCC[A/G]AGATCACACCACTGC	57674
rs180823247	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285622	GATGACGCCACTCTA[C/T]AGTGCTGGGCCCCAG	57674
rs180824947	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80344602	ATCCAATATAGATAA[C/T]GTGGAGGGTTAAGAC	57674
rs180826668	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297659	AGGCATGGTGGCGGG[C/T]ACCTGTAGTCCCAGC	57674
rs180829743	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393680	GAAAGCCGAGCTGTT[G/T]CTGAACCATGTACAT	57674
rs180831145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359388	AAAATTAGGCATAAC[A/G]TGGTGCGCACCTGTA	57674
rs180836679	snp	C/T	0.000479612	0.0154782	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374620	GGCTTCTCTCTGATA[C/T]CAGGTGGCATCCCTT	57674
rs180842336	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300592	GGAGTTTCGCTTTAT[C/T]ACCCAGGCTGGATTG	57674
rs180850512	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80316558	ACAGGAGCTGGAGCA[C/T]GAGAGGAACGGGGGT	57674
rs180859236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329149	AGCCTTTGCCTGGCA[C/T]CTGGGTTAGACGTGG	57674
rs180861300	snp	C/T	0.000430699	0.0146685	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319488	AAATCTAGTTCTCTC[C/T]GGATTCCTCAGTGTG	57674
rs180865231	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80340773	TTACAGGTACCCACC[A/G]CCATCCCTGGCTAAT	57674
rs180877466	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357490	AGTTCCAGATAAACA[A/T]GTGCCTTCTTGTTTA	57674
rs180881932	snp	C/T	8.25403e-05	0.00642365	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363145	CTAGGAAACTGAAAG[C/T]GGCGTCAGAAGCGCC	57674
rs180884579	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372169	TGGCATTTACTTGCA[C/T]ATACATACAAAACAG	57674
rs180890288	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335845	AGCCAGGCGTGGTGG[C/T]GGGCGCCAGTAATCC	57674
rs180908666	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80281753	CACAGGGGGTCGGTT[C/G]CAGGACCGCGGAGGA	57674
rs180915406	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397087	AGAGGACAGCCACTT[C/T]CTCAGAACCCACGAT	57674
rs180917833	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349190	GATACCGCAGGAACG[A/G]ACAGCAGGTTGTGGG	57674
rs180935088	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380390	TGCCACTGAGAGCAT[C/T]GGCCACACTGCATCT	57674
rs180960440	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265526	CGAAAACCAAGAAAT[A/C]CAGTGATGCTGGCTG	57674
rs180962462	snp	G/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80289314	TGGAGGCTGGGCCAG[G/T]CGCGGTAGCTCACAC	57674
rs180974198	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389631	CAAACAGCGTGATGT[A/G]AGCGGGCTGTGAGGT	57674
rs180987393	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80273034	CTGTCTGATTCACCC[C/G]TTGTTGTGCTGAAAC	57674
rs180992139	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310203	TTTCACCCACTTGAG[C/T]TCATGAGTTTCAGTT	57674
rs181142554	snp	A/G	6.66933e-05	0.00577427	missense	RNF213	GRCh38.p7	17:80340151	CTACCAGCTCGTCAT[A/G]GTCTGTGATGGGGAC	57674
rs181143516	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357400	ACCCATCTGTCCGTC[C/T]GCCCATCTATCCATC	57674
rs181148698	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80349974	TGGCTTCTGCGTGGC[A/G]ATGGTACCCGCGCCG	57674
rs181158350	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371581	TAATTCCTAATATCA[C/T]AAATATTGATAATAT	57674
rs181158605	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363904	CCTGCCATGGGAGGG[A/G]CTCCGTCCTCACCCG	57674
rs181165702	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381998	AAGACCTGCGGTATT[C/T]GGGAGCGTCTGCACG	57674
rs181165795	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388974	TTCCTGCTCTCCGCA[G/T]GCGGGTACTGATAGG	57674
rs181172700	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398700	GAGGAAGAGACAGAC[A/G]AAGAGGGAGTCAGAG	57674
rs181258055	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281334	ACACCACTCACACAC[A/G]CCCCCACACACACAC	57674
rs181293013	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280240	AAATGTGAGAAGGAA[A/C]TTGTAAAATAAAGGA	57674
rs181298782	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264069	ACCCGAGTGGGAGGA[C/G]AGGGCAGGGCCAGGG	57674
rs181298924	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300025	GCTTCAATGAACATA[C/G/T]ATGGGCATGTTTCTT	57674
rs181310243	snp	C/T	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80318864	AGGCGTGAGCCACCG[C/T]GCCCGGCCTATATGT	57674
rs181503291	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280112	TGGGCTGGGGCTTGG[A/C]CGTGAGCCCACTCCT	57674
rs181521536	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363525	AGCCTGGGACACAAG[G/T]ATACATGCAGCTAAC	57674
rs181553614	snp	A/G	0.0788843	0.182262	intron-variant	RNF213	GRCh38.p7	17:80273611	CCTGGGGCCTCCACC[A/G]TCTTTTTTTTTTTTT	57674
rs181579968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290324	GTGCGTGTGCGTTCA[C/T]GTGTGTGTGCGCACG	57674
rs181586778	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80310578	TTTTTTTGAGACAGA[A/G]TTTCACTCTTGTTGC	57674
rs181588077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329780	AGGCTGCAGTGAGCC[A/G]AAATCACGCCACAAC	57674
rs181596014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268095	CAAAGTACCGGGGCT[A/G]TAGGCATGAACCATT	57674
rs181597352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349474	CTGAGCCCTAAGGGA[C/T]CATGAGAATCTCAAG	57674
rs181601011	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304262	ACATTTTGGGTCTCC[A/G]GTACTGTGTTCCAGA	57674
rs181605402	snp	A/G	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80284241	TGATGGCAGGTGCCT[A/G]TAATCCCAGCTACTT	57674
rs181621818	snp	C/G	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355385	GAGCTTACAGGGGAA[C/G]AAGCGGGGTGAATGG	57674
rs181623719	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263024	GGCCAAGCGCCCAAA[A/C/T]GCCATCTCCACTCTC	57674
rs181627769	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367327	TGTTTCTCTAAAAAA[C/T]GATCTATCGCAGCAG	57674
rs181633044	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384492	AACATTTCTCTCCAT[C/G]GACTATTATTTGCTG	57674
rs181646513	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381061	CAGGGAGTCCTTTTG[C/T]CTTGAGTCCTAGCTG	57674
rs181691413	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318763	TATTTTTTGTAGAGA[C/T]GGGGTTTCACCGTGT	57674
rs181708190	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357066	TGGGATTACAGGTGC[C/T]TGCCACCACGACTGT	57674
rs181728204	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80296149	TTCAGCCTCCTTAGT[A/G]GCAGGGACTACAGGT	57674
rs181729267	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393882	CTCTTTTTTTTTTTC[C/T]TCTAATTCTGTACTC	57674
rs181811103	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366615	AGGATATTAAAAATA[C/T]ACACATCACTTCCAA	57674
rs181817555	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80339055	GTGGGTTGTGTAGAT[A/G]AGGAGGGAGGCCTTG	57674
rs181839742	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398187	GGTTTTGGTTTTGAC[C/G]TGACTTGGATATCCT	57674
rs181931090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316317	TCCCTGCCAAAAATA[C/T]TTTAATCTGAATCAA	57674
rs181965032	snp	G/T	0.00131707	0.0256281	missense	RNF213	GRCh38.p7	17:80345585	GTGGGATCCCGGTTA[G/T]CATCATGGGAGAAAC	57674
rs181980086	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375216	GGCTGCTAAATATGC[A/G]TTGAGTTTAATCTGA	57674
rs181999895	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80276607	GTGAGATCCTTCCTC[A/G]AAGAGAGAGAGAGAG	57674
rs182011567	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80294407	AAGGAAGTTGTTGAT[A/C]AAGTTTGCTGAGCTA	57674
rs182020565	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316082	GAACATGCCTGACCT[A/T]AGAAAAGTTCATTTT	57674
rs182033924	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334029	TGGGGCTGCTGGGAC[A/G]GTCAGTGCTTGCAGC	57674
rs182041523	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354860	AGTAGAACATTTACC[A/G]ACATTCATGTTGATA	57674
rs182093874	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392616	CTGGGTTTTTTTTTT[C/T]TCTCGCTCTGTCGCC	57674
rs182173342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277356	TAATCCCAGCACATT[A/G]GGAGGCTGAGGCGGG	57674
rs182201647	snp	C/T	0.00112101	0.0236484	synonymous-codon	RNF213	GRCh38.p7	17:80346933	CCCGCTGCTGGAAGA[C/T]GGATGCATTGAAGAC	57674
rs182206172	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360861	GGCCTTCTTTTCTAG[C/G]TTACCATTCTGCCAC	57674
rs182216068	snp	C/T	0.0154538	0.0865337	intron-variant	RNF213	GRCh38.p7	17:80274572	GAAGTGATGCAGCCG[C/T]AGTGCTGTGGTCTGT	57674
rs182230203	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80291111	GCCACTGCGCCCAGC[C/T]TTTAAATAATTTTTA	57674
rs182251620	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270019	ATAGCACGAAGTTTC[C/T]TCACCCTGGGCCAGG	57674
rs182252299	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394765	AACTGTGCTCCGTTC[A/T]CCTCACTGTCATGGT	57674
rs182254765	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80305808	TATTTTTAGTAGAGA[C/T]GCAGTTTCACCGTGT	57674
rs182255742	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384338	GGCGTACGTGGAAGA[C/T]GGGAGTGAGTGGGTG	57674
rs182259605	snp	A/G	1.67711e-05	0.00289573	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360026	TGAGTGACGTCTCAC[A/G]AACCCTCTTCTTATC	57674
rs182387730	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392025	TGCCCGTCTCGGCCT[C/T]CCAAAGTGCTAGGAT	57674
rs182465112	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80342858	ATGCCCAGGCTGGAG[C/T]GTAGTGGTGCAATCT	57674
rs182466675	snp	A/G	0.0119091	0.0762411	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358633	ATAGGAAGTTTGGCC[A/G]GGCATGGTGGCTCAC	57674
rs182477067	snp	C/G/T	0.00549304	0.0521195	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373212	TGCACCCCCACAGCC[C/G/T]CATACACCCCAAACC	57674
rs182518650	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285895	TGGCCAGGCTGGTGG[C/T]GAACTCCTGACCTCC	57674
rs182545226	snp	C/T	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80266901	TAGCTAGGCCTCTTG[C/T]ACCAAATGGTTAGCC	57674
rs182554101	snp	A/C	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80302772	GGCTTACATGAGAGG[A/C]TCGCTTGAGCCAGGG	57674
rs182560040	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80282240	TATGAACAGTTGCTA[C/G]ACGGTGCGGTGTTGC	57674
rs182563019	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320582	TTTAGAAGAGACAGG[A/G]TTTCTCCATGTTGGT	57674
rs182622386	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331497	AGGTTCAAGTGATTC[C/T]CCTGCCTCAGCCTCC	57674
rs182733073	snp	C/T	0.000494576	0.0157176	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364508	CGAGAGCCGCGTCCC[C/T]GAGTTACAGGGGCTG	57674
rs182741137	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307102	TTCAATCTTTTGTCC[C/T]GTTTTTCTTTTTTTC	57674
rs182780737	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372803	AATTCAGGAAGTATG[G/T]GAAACTAGTTCTTCG	57674
rs182812048	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312776	GAGCACACAGATGCC[A/G]TTCCCTCCCTCCCTC	57674
rs182819514	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80311004	TTGGTGAGATGATCA[C/T]GTTCTCTGGAGTGGC	57674
rs182827026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331841	GGTTAACAAGGCCAA[A/G]CGGGGAGGGAAAGAC	57674
rs182830375	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80271058	AGTGCCAGGGTAAAT[A/G]TCGGCCCTGATTGGA	57674
rs182832812	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352383	GCATGTAGGTCACAC[A/G]GCGTGGAGACTCCCG	57674
rs182836475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365120	CACGCAGTGGTGTCC[A/G]GCAACAGTGGCCACT	57674
rs182858403	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390299	TTCTTACCACAGAAT[C/G]CCATTTCCTGCTTTT	57674
rs182879853	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274722	GGGGTGAGTGTGGGG[A/G]GTGAGTGGGGTGTCT	57674
rs182881172	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312162	AAAAGAAAAGAAAAA[A/G]ACCACACATTAATCC	57674
rs183001511	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351469	GAAGAAAACGAGCCG[C/T]TAAGAGAAGATTTCT	57674
rs183020319	snp	C/T	0.000396576	0.0140759	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382950	TCTTTGTGCCTTGGG[C/T]AACCTACACATTTGG	57674
rs183042663	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80270295	GTCCTGCTGTTTTGC[C/T]GTGACATAGGCTGCT	57674
rs183047020	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387325	TTGCCCGGCTGGTCT[C/T]GAACTCTTGGGATCA	57674
rs183053516	snp	A/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80306648	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	57674
rs183056924	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286362	AAGGAGGAGAAAATC[A/G]GAATTTCTGGCCCTG	57674
rs183065313	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80325782	TGAGACCTTAGATTC[A/G]TATCTTTCAGTGAGA	57674
rs183069352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388211	CTTCGTGATCTGCCC[A/G]TCTCTGCCTCCCAAA	57674
rs183105956	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298205	TCTGCTCAGCCACGC[A/G]CGGTGCTCCTCTTGC	57674
rs183109497	snp	C/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80277706	CTGGTGATGAGTTTA[C/G]AGGGGCTTTTGCGCA	57674
rs183114687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317102	GCTCTCTGTATTGCC[A/G]TAATGCTCTGTCTTT	57674
rs183128134	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80272147	AAATTAGCCGGGTGT[A/G]GTGGCATGCACCTGT	57674
rs183136871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336150	CTGAACTCCCCTCTT[C/T]TCTTCCCCAGGCATC	57674
rs183139909	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80331115	TGAGCCACTGTGCCC[A/G]GCCTGGACCGTGTCT	57674
rs183142237	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355637	AATGGGGGCTTACAG[A/G]GGAAGAAGCGGGGTG	57674
rs183147707	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274347	GGCGAGGCTTTCGAG[A/G]GGAGCGTCCTGGACA	57674
rs183153139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368736	CCACACCTGGCCGAC[A/G]CCACTGGTTTTAATG	57674
rs183156391	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391347	GCAATCTTGGCTTAG[G/T]GCAACCGCTGCCTTC	57674
rs183284665	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383414	AAAATGAACTGACAA[C/T]CATAGATTAATTATT	57674
rs183330576	snp	A/G	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319842	CTCCCTGCTGGCCAC[A/G]GCTGCCCTGCTCACA	57674
rs183343133	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357886	CTGTCTACTTGCACG[A/G]CTGAGGTGGGAGGAT	57674
rs183408760	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290891	CTCAGCTCACTGCAG[C/T]CTCCGCCTCCTGGGT	57674
rs183410259	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80281769	CAGGACCGCGGAGGA[C/T]GCCAAAATCCAAGGA	57674
rs183440973	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259232	CAGCACTTTGGGAGG[C/T]CAAGGCAGGTGGATC	57674
rs183482560	snp	A/G	0.00164361	0.02862	intron-variant	RNF213	GRCh38.p7	17:80298570	GGAAGACTGACTCCT[A/G]CATTGTGCACCCGGA	57674
rs183572017	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394365	CAGTGTGCTCTCGCA[C/T]GTATGAATATCTAGT	57674
rs183573969	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80341409	TGTTCTGTTGACTTT[A/T]TCCTATCAACAGTAC	57674
rs183590176	snp	C/T	0.000798403	0.0199641	intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360358	TAAGCGTCCAATTTA[C/T]GTCACCGCGTCATTT	57674
rs183597986	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337013	GGGCCAGCCTCCGGA[C/T]GGCTGCTCTGCATGT	57674
rs183631135	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80266219	GGCCGAGGTGAGTAG[A/G]TCGCTTGAGCCCAGG	57674
rs183655048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377337	ATGAAATATAGAACC[A/G]GGAGACTGACTCATA	57674
rs183681447	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301133	TTGCTGTGCAAAAGC[C/T]CCTCAGTTTAATTAG	57674
rs183696985	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279492	TTTTTTGAGACAGAG[C/T]CTCGCTCTGTCGCCC	57674
rs183704497	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259847	CGGTTAGGAGGGGTG[A/G]CTGTCGAGGATGTTG	57674
rs183705931	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80299038	AACCTCAGAGGCAGC[C/T]GTTGTTAGCACGGTG	57674
rs183710283	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80279221	CCTGGAGAAACTTAA[C/G]CTGGCTGCACTCACC	57674
rs183717270	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318366	CCCGCCCCTGTCTGC[A/G]TAGGATTTCTCTGCC	57674
rs183719984	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307578	TTTTGAGATGGAGTC[G/T]CACTCTTGTTGCCCA	57674
rs183720352	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80317751	CTCTCTTAGCTCCGC[C/T]GTCTATGGACAGTAG	57674
rs183807258	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80304493	AAAATACAAAAAATG[A/T]GCCGGGCGTGGTGGC	57674
rs183808267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285529	GCACCTGCCTGTTTC[C/T]TGACGGCCTCTTGCT	57674
rs183819836	snp	C/G	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376092	AGATAATGTTTAACA[C/G]AATAGAATATCAAAA	57674
rs183821612	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365700	GCTGAAGGAAAAGGC[A/G]GAGAGAGGATAGTAG	57674
rs183821669	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80322545	TGTGCCACTGCACTC[C/T]GGCCTGGGCGACAGA	57674
rs183821880	snp	A/G	4.98484e-05	0.00499216	intron-variant	RNF213	GRCh38.p7	17:80344045	GCGTTTTCGCCTGGC[A/G]TGGGGGGCTCTTGGG	57674
rs183828406	snp	C/T	0.000150536	0.0086744	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383663	GAATTTTTTTTTTCA[C/T]TTTCTCCATCCAGCA	57674
rs183836827	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359259	GCCCAGGCTCGGTGG[C/T]TCATGCCTATAACCC	57674
rs183866854	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361290	TTGGGAGGCCAAGGC[C/T]GGCAGATCACCTGAG	57674
rs183881569	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268121	CCATTGCACCTGGCC[A/G]ATTTTATTCTTTTTT	57674
rs183927678	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395475	CCTTCACATGTGAGA[C/T]GGTGGACTTTTCCTC	57674
rs183930167	snp	A/T	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80275412	AAACCCTTTGCCATC[A/T]GGGGCAAACAATAAA	57674
rs183935966	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320749	CACGCCTGTAATCAC[A/G]GCACTTTGGGAGCCC	57674
rs183937996	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287605	CGAGTGTGGCGAGCG[C/T]TTCAAGGCCACTTGC	57674
rs183941195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327359	TTGAAAGTTTGCCAG[A/G]CATGGTGCTGTGCAC	57674
rs183953855	snp	A/C/T	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80293181	TCCCCCTCAGCCCCC[A/C/T]CAAGTAGCTGGGCCT	57674
rs183957213	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314357	GGTGGTGGAGGTACT[A/G]GAGGTGATGGCGGTC	57674
rs183996049	snp	A/G	0.00835141	0.0640778	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396716	AAAACAAGCGCCAGG[A/G]AAGTGCATTTCCCCC	57674
rs184039435	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349167	GTGGACATTGCTTCA[A/T]CATGACAGATACCGC	57674
rs184055393	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362647	GGGCTGCGTGGCAGA[A/T]CAGTTGAGCACCTTA	57674
rs184062025	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379835	GTACATGTGGGCCTG[C/T]GTCATATTGAATAGC	57674
rs184252795	snp	A/T	0.00159617	0.0282053	intron-variant, missense	RNF213	GRCh38.p7	17:80288915	TTCCAGCGGAGAGAG[A/T]GTCAGGAAACCGACT	57674
rs184270481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267548	GGAGAGGTCAAACCA[A/G]TCACAACATTCCCTT	57674
rs184293136	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355883	CTCGTGACCAGAGAT[C/T]TTCTGATTCTACTTT	57674
rs184370754	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272378	TTCAGGGCCTGGCCC[C/T]GATGTCTGGTGAGGG	57674
rs184373913	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267233	AAAAAAAAAAAAGAA[A/G]AAAAAGAGACCATCC	57674
rs184401609	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80337403	CACTGAGTGACAGAT[A/C]ATGTTGTCAGGGTGG	57674
rs184401645	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272723	GGGCTGGCAGAGTGG[A/G]TGCTCCATGCTGTCT	57674
rs184406341	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80309482	CTGGGGGTCAGGCAA[C/T]GCCACGCGGAGAAGA	57674
rs184448645	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366471	TGGTTTTTATTTGCA[C/T]TTCTCTAATGACTAG	57674
rs184474799	snp	A/G	0.00159617	0.0282053	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288000	TGGCCAGCCGAGCCA[A/G]CCCCCAGGCACAGCC	57674
rs184483981	snp	A/C/G	0.00269949	0.0366405	intron-variant	RNF213	GRCh38.p7	17:80308969	GGTAACCATTTTCTG[A/C/G]CTTCTCCTAAATCCT	57674
rs184485888	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327642	AGACCTAACCCTCGT[A/G]GGGGAAAGCAGAAGG	57674
rs184498344	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348666	ATATCATATGATAAA[C/T]GCTGTGCTTAGAGGC	57674
rs184503889	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80362060	GCCCAGTCTCCTCTC[A/G]ATATTCAGTGCTACA	57674
rs184508863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303093	GGAAGTACTACTCAA[A/G]GCACAGCGTGTACAG	57674
rs184522458	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282584	TTTTGTATTTTTGTA[A/G]AGATGGGGTTTCACC	57674
rs184532862	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333372	GCTGAGTCTTCTGCT[G/T]CTTATGTTTTTAGGT	57674
rs184565768	snp	C/T	0.00557542	0.0525036	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352680	CAGGCCTTATCCATG[C/T]GTCCTTCCCACGCTG	57674
rs184593439	snp	A/T	0.00294502	0.0382601	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374441	TTGTTCACCCCCAAC[A/T]AACCTCTGTATTCCA	57674
rs184621372	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80274955	GGTGTGTGAGTGGGG[G/T]GTGTGTGTGTTGGGG	57674
rs184635632	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274789	GGGTGTCTGTGGGGG[A/G]TGAGTGGGGTGAGTG	57674
rs184644421	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80313183	GTAGGCATTTGGCCG[A/C]AGGCTTCTGGGTAGG	57674
rs184653933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388970	TTTGTTCCTGCTCTC[C/T]GCATGCGGGTACTGA	57674
rs184672079	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353402	CACCACAGCAGGGGC[C/T]GGGGAAGCCTGCACT	57674
rs184681719	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80332740	CGGATGACTTAGAGC[G/T]TCCGTCAGGGGCTCC	57674
rs184733392	snp	C/T	0.0433465	0.140692	intron-variant	RNF213	GRCh38.p7	17:80318604	TTTGAGACGGGGTCT[C/T]GCTCTATCGCCCAGG	57674
rs184734837	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337527	GCCGACCACAGGAGG[C/G]AGAAGGGCAAGATCC	57674
rs184744673	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356445	CACCGTGAGGCCTGC[A/G]CAGCCGCTGAGTGGT	57674
rs184752886	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370992	GGGGCAATTTGTGGT[A/G]ATATTAATGAATATG	57674
rs184760829	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388778	ACTCCAGCCTTGCCC[C/T]GGGTGTTTGCTGTGA	57674
rs184771914	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292773	CCGCCTCCTCACCTG[A/G]GGGGTCCTGGGCTTC	57674
rs184802580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299334	CATAAGCATCCTTAG[C/T]TTTCTCTGTCCCATA	57674
rs184831226	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328705	TCTCCTGGATTTTTC[C/T]GGAGTCAGCATGAGC	57674
rs184831757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393236	CCCACCCACCTCAGC[C/T]TCCCACAGTGCTGGG	57674
rs184941086	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370333	TCACCTGTGGTACTT[G/T]TATGGATCTAATATT	57674
rs184963202	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316134	GCTGATGCCTGTAAC[A/C]CCAACTCTTTAGGAA	57674
rs184978779	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334058	GCTCACAGATTCTGG[A/G]GTTCTGGTTAATGAG	57674
rs184980804	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355069	ATCTTGGATGTGGCC[A/G]TGTATTGAGGAAGGA	57674
rs184995913	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366898	CAAATTCCATTAGTA[C/T]AGCCATTAAACTATC	57674
rs184999620	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80281121	CCCCACTCACACCAC[A/T]CACACACACCCCCAC	57674
rs185001808	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384430	TGGAAATATACTTTC[C/T]TAACTTTCACCCATT	57674
rs185026622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264426	GCTGAGCATCTTGAG[C/T]CCATTCTCAATTTTG	57674
rs185091260	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80283319	CTGGGGCTGCTGCTC[C/T]GAGGTGTCAGCCCTG	57674
rs185110638	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321788	GAGTGCAGTGGCGTG[A/T]TCTTGGCTCACTGCG	57674
rs185174542	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80298086	CTTCTGAGATCCCTC[C/G]CCTGTCCTGGGAGTT	57674
rs185187820	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80316944	TTCAGAATAAAAAGC[C/T]GGTTGTGCAGTAGGA	57674
rs185189079	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359659	AGAAAGAAATGGAAT[C/T]TGAATTGCCAGTGGA	57674
rs185192115	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80335907	ACTTAAACCTGGAAG[G/T]TGGAGGTTGCAGTGA	57674
rs185195273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374783	CCAGTGGCTGGAACA[A/G]GACAGCTATGACAGT	57674
rs185210870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303654	CTGCAACCTTCGCCT[C/T]CCAGGTTCAAGTGAT	57674
rs185230945	snp	C/T	0.000494071	0.0157096	synonymous-codon	RNF213	GRCh38.p7	17:80343895	TCTTTTCAAGCTCCT[C/T]ATTTTACAATACTTA	57674
rs185234128	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393846	TGACCTGTGCCCGTT[C/T]GCCTCTGGCACTGCC	57674
rs185261320	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277436	AACCCCGTCTCTACT[A/G]AAAATACAAAAAGTA	57674
rs185283816	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371259	ATTTATCACTGTGGG[C/T]ACAGCATTAAGGAAT	57674
rs185321737	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263164	GCGCTTTGTGGATGG[C/G]AGCCTCCCCCCATTA	57674
rs185352986	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80299884	TATGTTCCTGCAAAG[A/G]ACATGATTTCATTCT	57674
rs185359498	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395720	TAAACAGTAACCCTT[C/T]CAGGAGCCCACTGAC	57674
rs185365088	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80339076	GGAGGCCTTGTGAGC[A/G]CAGATCATGCAGTGG	57674
rs185388302	snp	A/G	0.0490535	0.14873	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357137	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	57674
rs185456778	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80279991	CCCCAGCCCCTGCCC[A/G]TCGAGATGGTCATGT	57674
rs185486509	snp	C/T	0.0174175	0.0916809	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379048	GGGCATGGTGGTGCA[C/T]GCGTGCATGCGTGCA	57674
rs185513076	snp	C/G	0.000644112	0.0179344	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380789	CAGCGTGCCAAAGCG[C/G]CCAGCCTCAGCCTCT	57674
rs185523753	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300029	CAATGAACATACATG[A/G]GCATGTTTCTTTATA	57674
rs185530330	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80280550	CCTTGACTTCCTGGG[C/T]TCAAGCAATCCTCGT	57674
rs185535624	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363428	TTCTTCACAAGGCAC[A/G]TACCTTAGCTGAATT	57674
rs185535834	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318958	ACTTACCTGTTTTTG[C/G]AAGCCAGGTGCTTTT	57674
rs185552839	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80340682	CTGGAGTACAGTGGC[A/G]TGATCTTAGCTCACT	57674
rs185553427	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286473	GCCCTGTCCAGCTGC[A/G]GCCTCGTCATGCCCT	57674
rs185565103	snp	G/T	0.00993419	0.0697739	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261277	GACCCGGGCCTGCAG[G/T]TCCGCCCGGGAATCC	57674
rs185579124	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392658	GCAGTGGTGCAATCT[C/T]GGCTCACTGCAAGCT	57674
rs185611271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358937	GGAAGTTTACGAAGC[C/T]CTGAGAAATTTCTGT	57674
rs185620803	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397440	ACAGCCTGCACCACA[C/T]CCTGGGCCTGGTAGT	57674
rs185662432	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80306811	GAGCCGAGATCACGC[C/T]GCTGCACTCCAGCCT	57674
rs185670413	snp	C/G	0.000198423	0.00995851	missense	RNF213	GRCh38.p7	17:80346461	GGAAAGCCATCGCCA[C/G]GTTCTTTCCGAAACC	57674
rs185674780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384958	CAAATACAAGTCTCG[C/T]AGCCAGTCTCAAAGT	57674
rs185679324	snp	A/G	0.00279162	0.0372561	intron-variant, synonymous-codon	RNF213, LOC100294362	GRCh38.p7	17:80360359	AAGCGTCCAATTTAC[A/G]TCACCGCGTCATTTT	57674
rs185689608	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376182	TTTCCCCCTCAAATG[A/G]TGGTGATTTCTCCAT	57674
rs185713484	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363959	TAGTGAGTGCCAGGC[A/G]TCTCATTAGGGTGCT	57674
rs185721387	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382096	CCATGCTGGGAGCAC[A/G]TGTCGTCCACACAGA	57674
rs185754025	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373639	TGCAAGGTGCGACCT[C/T]TTTACCTCTGGCAGG	57674
rs185772219	snp	A/C	0.00159617	0.0282053	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398829	TTAGAAACAACAACA[A/C]CACTGTACCCTATTC	57674
rs185936062	snp	C/G	0.000399281	0.0141238	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385547	CAACAGATGGGTTGA[C/G]GCAGCTGCTTCACAA	57674
rs186037056	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80295304	CCCACACTGCGGTGC[A/C]GCCTGGGTGGGTTTC	57674
rs186096141	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368322	GTATCTCAAGATTAT[G/T]CTCTCCCCAAGACAT	57674
rs186105401	snp	A/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319650	TTTGATTGATTGTTA[A/T]CACTTGCTCAGTAGG	57674
rs186150245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304846	TTCCCCAGCTGAAAC[C/T]CCATCCCCATGAAAC	57674
rs186174750	snp	A/G	0.0263992	0.111815	intron-variant	RNF213	GRCh38.p7	17:80277080	CAAACAAACCAAAAA[A/G]AAAACAAAAAAAGAA	57674
rs186175310	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389754	GTGTGGAGAGCACTC[A/G]GGCTCCCTGGTGCAC	57674
rs186186109	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80316423	TCAACATGTTAAAAG[A/G]AAAAAGAAAAAAATG	57674
rs186191445	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80322595	AAAAAAATTTTTTTT[C/T]GTAGAGACAGGGTCT	57674
rs186197293	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330179	CCTGTTCTTGTTCAC[G/T]TTGCAGCATCTTCCC	57674
rs186199321	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310822	CTCCCAAAGTGCTAG[A/G]ATTACAGGCATGAGC	57674
rs186214518	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349683	GCGCTGAACATCGCA[A/G]GTTTCTAGGATCTGT	57674
rs186219139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340868	GGAGTACAGTGGCGT[A/G]ATCTCGGCTCACTGC	57674
rs186220836	snp	C/G	0.000133485	0.00816851	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363665	GACAAGAAACACCCT[C/G]AAGCCCAGTCCCCAG	57674
rs186221365	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357745	GGGAGGCCAAGGCGG[A/G]AGGATTACTTGTGCC	57674
rs186229511	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381418	CACCTGGATCACTCC[A/G]CCGTTTTCATCTTAG	57674
rs186232347	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372324	TTTTTTTCCTCATAG[G/T]TTCACTTTTCCCCTC	57674
rs186243657	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398256	ACTGTAAAAGTGTGT[C/G]TGTGCCCTTTTTACC	57674
rs186264023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285732	CTGGAGTGCAGTTGC[A/G]TAATATCGGCTGACC	57674
rs186267756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274095	GGCAGGGACCTGAGC[A/G]TCCGCTGGGTGCGTG	57674
rs186289981	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273162	ATCTCTCCATGCACT[A/C]GTGGGGAGGATTTCT	57674
rs186294080	snp	A/G	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80289605	CAGAAAAAAAAAAAA[A/G]AAAGAAAATGTGGAG	57674
rs186350190	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389036	CTGCCTGCACACCGT[A/G]CGCCCAAGTGTCAGC	57674
rs186351243	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80335626	ACAGAAGTGCAGTAC[A/G]GTGCCTGGGACATTG	57674
rs186408544	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80291055	GACCTCAGGTGATCC[A/G]CCCGCCTAGGCCTCC	57674
rs186419475	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394517	GACGTGTTGCCTTTT[C/T]TCTTTACAAAATCTG	57674
rs186460768	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357408	GTCCGTCCGCCCATC[C/T]ATCCATCCACCTGTC	57674
rs186463204	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331292	TGTTACCAGGCCTCA[A/C/T]GTGTCATTTACCACT	57674
rs186478585	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80285896	GGCCAGGCTGGTGGC[A/G]AACTCCTGACCTCCA	57674
rs186482824	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80270124	CGCACACACACACAC[A/G]TTAATGTGAGTGGCA	57674
rs186490932	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367375	AAATTTTAAAAAATT[G/T]AAAAATTTTAAAAAA	57674
rs186555700	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80350105	CCTAACATCCTCCTC[C/T]GAGAGCACCATCCTC	57674
rs186625529	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394948	AACGGGTGTGGGGGC[C/T]GGGGGCTGGCTTGCT	57674
rs186643053	snp	A/C	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80318432	GGGCCAGGCCTGCCC[A/C]TAGGCAGGAAGTCTA	57674
rs186643724	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80274471	TGGGCACGGAGAAGG[A/G]GAAGCTGTCTTTCTG	57674
rs186644794	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311497	GGCCCCCGCCCCCTG[C/T]GTGCTGTGCTCTAGT	57674
rs186656572	snp	C/T	0	0	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360997	CCGCCCACTAGAAGC[C/T]AGATCTTTCTGGCTT	57674
rs186658498	snp	A/T	0.000214254	0.010348	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371853	CTGAGAGAACCAGGA[A/T]TAATATTTCTCTTTC	57674
rs186662586	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80337448	GGGGCGCTGGGTGGG[C/T]GACTGCGTCCTGAGC	57674
rs186662835	snp	C/T	0.000399281	0.0141238	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376446	TTGATGGAACGGTGA[C/T]AGAAATGGCCATTCA	57674
rs186668769	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355924	ATCCTTCGTTTCTCT[C/T]CTTGTCACGCCTTCT	57674
rs186749717	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315779	TGATGCTGGTGGTGG[A/T]GGTGGTGGTGGTGGT	57674
rs186814177	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390841	GCCGAGGTGGGTGGA[G/T]CACCTGAGGTCAGGA	57674
rs186912481	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80341876	CAATGGCACGATCTC[A/G]GCTCACTGCAGCCTC	57674
rs186912978	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80276897	CTCTACTAAAAATAC[A/C]AAAAAAAAAATTAGC	57674
rs186920237	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260026	GAAGAAAAAGAAAGT[C/G]GGTGATTTTAAAACG	57674
rs186927851	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299080	TGTGGTTTTGTCCAA[A/G]TATGGATTCGTGGGT	57674
rs186934109	snp	G/T	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80279590	CTGCCTCACCCTCCT[G/T]AGTAGCTGGGATTAC	57674
rs186938689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379242	ATAAGGAAGTCAGTT[C/T]GGAAGCTCTTCTAGT	57674
rs186975581	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395810	AAGGTTCTTCCAGGC[A/G]AGAAACCTGTGGTCT	57674
rs186996851	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310347	AATCTCCGCCTCCTA[A/G]GTTCAAGTGATTCTC	57674
rs187005449	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80270349	CTTGCCCTCTGAGCC[A/C]GGCTGGCCGTCTGGA	57674
rs187009909	snp	A/C/G	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80281761	GTCGGTTCCAGGACC[A/C/G]CGGAGGACGCCAAAA	57674
rs187012698	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80349357	ATGGGGGAGTGACCT[C/T]TGGGACAGGAGAATT	57674
rs187020004	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259271	TCAGGAGTTTGAGAC[A/C]ACCCTGGCCAACATG	57674
rs187120745	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357955	ATTGTGTCACTACAC[C/T]GCAGTTGGCGTGACA	57674
rs187186316	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80342777	TATATATATATATTT[A/T]TTGAGACAGAGTTTC	57674
rs187194050	snp	C/G	0.00020585	0.0101431	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358528	AACTATCAGAACACA[C/G]CAGGACCCTAATATG	57674
rs187205552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265780	TGCTGTTAAAGTGGG[A/G]GCACTTAAGCCGGAT	57674
rs187219940	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329290	TGTGTGTCTAAAGAT[C/G]TCTGTCCTCTTACTA	57674
rs187225420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300628	GCACAATCTCAGCTC[A/G]CTGTAACCTCTGCCT	57674
rs187248564	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80267107	CTGTAATCCCAGCTT[C/T]TTGGGAGGCTGAGGC	57674
rs187249289	snp	C/T	0.000351968	0.0132612	missense	RNF213	GRCh38.p7	17:80332216	GGGAAGCCGCAGAGC[C/T]GCTGAGTGAGCCTAA	57674
rs187252835	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352608	ACCTTGCCAGTGTCC[C/T]CCACCCCTCACTAAC	57674
rs187255859	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302795	AGCCAGGGAGGTCAA[A/G]GCTGCAGTGGTAGAA	57674
rs187257442	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282419	GTTATTATTTTTTGA[A/G]ATGGAGTCTCACTCT	57674
rs187269156	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383431	ATAGATTAATTATTC[A/G]TCTAGCAGCCAGAAT	57674
rs187294748	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324182	TCTGATCTTAAGAGA[A/T]GGTTTCAGTCTTTTG	57674
rs187300629	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394121	CACTTCAGAGGGTAA[C/G]AGCCAAAAGCCTCAT	57674
rs187312452	snp	C/T	4.95978e-05	0.0049796	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360085	TGAGATGGCCTACAT[C/T]GTGGTGCAGAACCAC	57674
rs187389872	snp	A/G	3.29582e-05	0.00405931	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375850	AGATCCCACAATGCA[A/G]GCCTCCACCCCACGC	57674
rs187469140	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306129	CACCACGCCTGCCCT[A/C]AAGTAGTATTTAAAT	57674
rs187481893	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291897	CCGCGGTACTGGACG[C/T]GTCTCTCTGGAGAGC	57674
rs187488899	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80312830	CAGGGTGAACCCAGA[A/C]AACCCTGGGGAATGG	57674
rs187502526	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370456	GCCCTTTTTTAAAAA[A/G]CATGTTGATACTTAT	57674
rs187567513	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274634	GTGGGGTGTCTGTGG[A/G]GGGTGTGGGGTGAGT	57674
rs187609658	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80266635	GCCTCCCAAGTAGCG[A/G]GGATTACAGGCGTGA	57674
rs187638120	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80275044	TGTGTGTGTGTTGGG[G/T]GTGTGTGTTGGTGTG	57674
rs187701500	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272020	CCGGGTGGGGTGGCT[C/T]ACACCTGTAATCCCA	57674
rs187714837	snp	A/G	0.000132166	0.00812807	intron-variant	RNF213	GRCh38.p7	17:80307247	TCACATGCGGCCCCC[A/G]GGGGCTTCCTCTGAC	57674
rs187719193	snp	A/G	0.000132551	0.00813991	missense	RNF213	GRCh38.p7	17:80347075	GAGCTCATAGAGAGC[A/G]CCAAGGGCATCTGCT	57674
rs187726161	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80291352	CTCAATCTCCTGGGC[C/T]ATCATGCCCAGCTTT	57674
rs187734199	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312605	GGGGACCCAGGTTTA[C/T]CTCCGGGTCAGGAGC	57674
rs187758824	snp	A/G	0.00119737	0.0244387	missense	RNF213	GRCh38.p7	17:80336349	CTGTGGAAGGCTCTG[A/G]ATAAGGACCAGTACC	57674
rs187760608	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388374	TGGCGAAGCAGGCCA[C/T]GATGATGTGACAATA	57674
rs187761779	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307792	TGACCTCAGGTGATC[C/T]GCCTGTCTGGGCCTC	57674
rs187762855	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287717	TTGGTCGAGCCAAGC[C/T]TGATGTAGTTGAGGA	57674
rs187775360	snp	A/C	0.02016	0.0983543	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368902	TCCTTCCCCTTCCCC[A/C]CTTCTCAGGCCTCCT	57674
rs187799453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358730	CCTGGCCAACGTGGT[A/G]AAACCCCGTCTCTAC	57674
rs187809329	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373324	CACACCTCACCCTCA[C/T]ACCCCCACACCTCAC	57674
rs187850880	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80272184	AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATTG	57674
rs187872859	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392403	GGCCTTGTTTATGCA[A/G]CCCTGTAAATAAACA	57674
rs187891743	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387801	TTCCCTGAACTGCAT[C/T]CCGTGACCTCATGCA	57674
rs187896153	snp	C/T	0.000127685	0.00798912	synonymous-codon	RNF213	GRCh38.p7	17:80343308	CCCGTGCTCTTTCAC[C/T]TGGACGTGACCTCCT	57674
rs187959673	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379931	TGAAATGCAAAGCAG[C/G]CTACCCTTTAACAGC	57674
rs187960957	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80317862	TAGGTACCCACACTC[A/G]GTGGGTCCCAAGCTC	57674
rs187963706	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357436	GTCTATCAGACACTC[A/T]GATCTAGTGTACAAA	57674
rs187972315	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355693	AAGAAGCGGGGTGAC[C/T]GGGAATGGGGGCTTA	57674
rs187973453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372095	ACGAATGCTCTGTTC[C/T]GTGCAGAAAAGAAGA	57674
rs188005990	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80326572	CGTGCAGAATAGTTG[C/T]GCTGCCCCTACAAAA	57674
rs188016983	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80332985	GTCGGCTGCCCAACT[G/T]CATCTCCCAGTTCCA	57674
rs188027943	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365923	GGATTTGGGAGGTTA[C/G]GAACGTGGGGAGGGT	57674
rs188037076	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391354	TGGCTTAGTGCAACC[A/G]CTGCCTTCTGGGTTC	57674
rs188037632	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396853	CGAAAGCAACCTGGG[G/T]CCAAAGCAGGGGGAA	57674
rs188167719	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369951	CCAAGTCTTCTTGTC[C/G]TGACTAGTAGCTAGT	57674
rs188194559	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393867	TGGCACTGCCCACCC[C/T]TCTTTTTTTTTTTCT	57674
rs188207064	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374844	GCTGATCTGCCAAGT[C/G]CATCAGCAGCGCCTT	57674
rs188249584	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337015	GCCAGCCTCCGGACG[A/G]CTGCTCTGCATGTGG	57674
rs188307071	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353128	AGGTGTGGAGCGTGG[C/T]GTGCACATGGCACTA	57674
rs188460299	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80348685	GTGCTTAGAGGCAGC[A/G]GGGAGCGGTGCAGAC	57674
rs188466571	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362309	AGGAGAGTGACAAAT[C/T]TAAGAACATCCTTAC	57674
rs188489730	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301588	CAAATCAAAACCACA[A/C]TGAGATATGGTCTTA	57674
rs188510056	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274742	GTGGGGTGTCTGTGG[A/G]GGGTGAGTGGGGTGA	57674
rs188523018	snp	C/T	1.64792e-05	0.00287042	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288766	GCCAGGTGCGTCTCC[C/T]TCCTGCCTGCCGGCT	57674
rs188539160	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280160	CAGGCAGCGTCCACA[C/T]GGGGCTGGACTTAGC	57674
rs188541240	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328061	CACGTTTGTGTTTGC[A/G]TGTGCATTTTTGTAA	57674
rs188543147	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80309262	AACAGACTGATTCCC[A/G]GGTGCTGGGATGAGA	57674
rs188545155	snp	C/T	1.65064e-05	0.00287279	missense	RNF213	GRCh38.p7	17:80263725	CCAAGGAGGAAACCC[C/T]CAAGTTCTGCAGCCA	57674
rs188563118	snp	A/G	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80269589	CTATACTATCTATCC[A/G]TCCATCCTATCTGTT	57674
rs188581750	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285546	GACGGCCTCTTGCTT[C/T]CCCCTCTCAGCAGGT	57674
rs188589132	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80304501	AAAAATGAGCCGGGC[A/G]TGGTGGCAGGCGCCT	57674
rs188589541	snp	A/T	0.0260105	0.111035	intron-variant	RNF213	GRCh38.p7	17:80322586	GTCTCAAAAAAAAAA[A/T]TTTTTTTTCGTAGAG	57674
rs188694295	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80344595	AAGGTCCATCCAATA[C/T]AGATAACGTGGAGGG	57674
rs188707433	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359360	GTGAGACCCCATCAC[C/T]ACAAAAAATTTAAAA	57674
rs188740576	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213	GRCh38.p7	17:80282649	GTGATCCACCCGCCT[C/T]GGTCTCCCAAAGTGC	57674
rs188753299	snp	C/T	0.000241134	0.0109777	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351682	TTTTTTTTCTTTAAA[C/T]AGGTATTCTGTTATA	57674
rs188756885	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321398	CAAATATTCCCCGTT[C/T]ATCCATGTGTCCATT	57674
rs188763264	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80281794	CAAGGATGCCCAGTC[C/T]CAGATATGAAACGGC	57674
rs188772617	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383312	GGGAATCCAGCAAGT[C/G]CAGGCAGTGTTTTTC	57674
rs188787035	snp	A/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319864	CTGCTCACATTTCCT[A/T]ATTGGACACTTAACC	57674
rs188798935	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327490	TGTCAAAAAAAAAAA[A/G]AAAAGGAAGTCAGTC	57674
rs188811079	snp	A/C	0.0193772	0.0965046	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361391	TGGGTGTGGTGGTGC[A/C]TGCCTGTAGTCCCAG	57674
rs188858084	snp	A/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80298516	GGAACAAATGCTAGA[A/T]ACGTAAGTCGTAGAG	57674
rs188880296	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367274	ATCTCTGGGGAGGGA[C/T]GGAGGGATGTGAAGT	57674
rs188891447	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384487	GTCTAAACATTTCTC[A/T]CCATGGACTATTATT	57674
rs188921610	snp	A/C			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395573	GGACTGAAACGCTTA[A/C]ACCTCTGCCTCAGAA	57674
rs188958917	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80316150	CCAACTCTTTAGGAA[A/G]CCTAGGTGGAAGGGT	57674
rs188961033	snp	C/T	0.000114097	0.00755217	synonymous-codon	RNF213	GRCh38.p7	17:80334194	GCTCCAGGACATCAG[C/T]GAGGCCCGGTGCAAG	57674
rs188969691	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355236	AGTCCCCTTCCAGGT[C/T]CAAGCTTCTGTGCCA	57674
rs189007207	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80267453	TCCCAAAAAAGAAAA[A/G]AAGTGCTACTCCAAT	57674
rs189028293	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331668	TGCTGGGTGGGATTA[C/T]AGGCATGAGCCACTG	57674
rs189030155	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80272901	AGTAGGGGAGGAAAG[C/T]GTAACAGGCTCTGTT	57674
rs189036617	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80309499	CCACGCGGAGAAGAC[A/G]ACTTTTCTTTTTTCT	57674
rs189040908	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80303125	ACTGCTCAAAACAGA[C/T]AGCTGCTCCTGGCCT	57674
rs189043763	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364741	TTGTTTAATTATTTA[C/T]CCTCTGCTGATTGCT	57674
rs189063217	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80349189	AGATACCGCAGGAAC[A/G]GACAGCAGGTTGTGG	57674
rs189076605	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80283874	TTGGCTTATTTTCAA[C/T]TTTCATAATTAGGGA	57674
rs189077033	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80268035	ATATTAGCATTGCTG[C/G]TCTCCAACTCCTTGA	57674
rs189080582	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348394	GTTAGGGATCCTGCA[G/T]GGAGATGCTGAGACG	57674
rs189100545	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377353	GGAGACTGACTCATA[C/T]AACCCATGACATGTA	57674
rs189138406	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277879	ACAGCGAGCTGCGTG[C/G]CCAGCCTCACCCTGC	57674
rs189287851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389575	AGAAATGCCAGCAGT[C/T]TAGATAGAGCCCAAA	57674
rs189310490	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80289243	GAAGGTCCCGAGCGG[G/T]GAAGGGTCGTGAACA	57674
rs189335409	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328863	GTTAAATCATCAGGA[C/T]CCACACGGATCACAA	57674
rs189350910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362972	CTGGACAGAAGCAAA[C/T]GGGACAGAATAGCAC	57674
rs189374832	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80333671	TGCACTCCAGCCTGG[G/T]CGACAGAGTGAGACT	57674
rs189391113	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354253	TGTGTGTTGGGGGAC[A/G]CCCTCTCAGGTTTCC	57674
rs189448282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276003	CATGTTTTGGCTGTA[A/G]GTGTTTAAGGAAATC	57674
rs189456330	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294332	CCAGGACAGTGCTCA[C/G]TTGCTAGTGGGGGGA	57674
rs189487651	snp	A/G	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80318863	CAGGCGTGAGCCACC[A/G]CGCCCGGCCTATATG	57674
rs189492831	snp	C/G/T	0.00116363	0.0240931	intron-variant	RNF213	GRCh38.p7	17:80273221	CTGAGATCTGACCCT[C/G/T]CCTTCATCTGCCGTT	57674
rs189503951	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357163	CTCAGGTGATCCGCC[C/T]GCCTCAGCCTCCCAA	57674
rs189505109	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80338897	AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC	57674
rs189514243	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290318	GGGTGTGTGCGTGTG[C/T]GTTCACGTGTGTGTG	57674
rs189520709	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388971	TTGTTCCTGCTCTCC[A/G]CATGCGGGTACTGAT	57674
rs189521535	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80340733	TCAAGCAATTATCCT[A/G]CCTCAGCCTCCTGAG	57674
rs189589480	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80265293	CTCAGGTGATCCACC[C/T]GCCTCGGCCTCACAA	57674
rs189590003	snp	A/T	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80293063	TGTAAACATATATAT[A/T]TATTTTTTTTCTGAG	57674
rs189597325	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300051	TTCTTTATAATAGAA[C/T]GATTTATATTGTTTT	57674
rs189599577	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280953	TGGAGTTAGGGCACT[A/G]CATATGCGGACCGGA	57674
rs189613378	snp	A/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356846	CTGTACTATATATTT[A/T]AAAAATGTAGGTATT	57674
rs189616288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318965	TGTTTTTGCAAGCCA[A/G]GTGCTTTTTCTGCAG	57674
rs189617322	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310362	GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC	57674
rs189619238	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329516	ATTCTGAAATAATAA[C/T]GTGTCTTGGCCTGGA	57674
rs189620284	snp	A/T	0.0197687	0.0974348	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371021	TGGATTTTTTTTTTT[A/T]AAACGTAGAATACAA	57674
rs189623700	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388820	CTGCGGCCTCCCTTA[C/G]AGAGAGCAAGCAAGA	57674
rs189758808	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80300016	GTGAATTGTGCTTCA[A/G]TGAACATACATGGGC	57674
rs189765261	snp	C/T	0.00103347	0.0227083	missense	RNF213	GRCh38.p7	17:80339529	TCAGGAAGCAGCCCC[C/T]GAGTGATGCCGCCCT	57674
rs189765635	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80336085	ATTTCAGCTTCAGTA[A/G]GGATTACTGCCCAAG	57674
rs189767839	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355635	GGAATGGGGGCTTAC[A/G]GGGGAAGAAGCGGGG	57674
rs189778000	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368426	CCCAAGGAATGTAGA[C/T]GCCAGTGTTTTTTTT	57674
rs189787769	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371324	GTTCCTCGCTATTCC[A/G]AGTATATGAGGACAG	57674
rs189795015	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398915	GTAACCCTGTAACAC[G/T]CCAATACCACTTTGT	57674
rs189813550	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272515	ATCCATTCCCGAGGG[C/G]AGTAAACAAGCCTCT	57674
rs189843062	snp	C/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80303743	ATGTGGCTAATTTTT[C/G]TATTTTTAGTGGAGA	57674
rs189860275	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80276920	AAATTAGCTGGGCGT[C/G]GTGGCGTATGCCTGT	57674
rs189866084	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80313526	GGTGATGGTGGTGAA[A/G]GTGATGGTGATGGTG	57674
rs189883986	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374088	CAAATTCTTATTGTC[C/T]AGGGGATACAAAAAT	57674
rs189947189	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395201	TGTCAAATCTTGCAT[C/T]ATCTTGTTTGTACAG	57674
rs190107217	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321914	TATTTTTGGTAGAGA[C/T]GGGGTTTTGCCGTGT	57674
rs190111205	snp	C/T	0.000268772	0.0115894	intron-variant	RNF213	GRCh38.p7	17:80295851	TGTTTTTTATAGCTA[C/T]TATAATGATTTTCTC	57674
rs190130163	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359113	CATTCCCTGGTGGAG[A/C]GGCACAGCCCCCACC	57674
rs190141986	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392714	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	57674
rs190174048	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80281943	CTCCCTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	57674
rs190182609	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310885	TACTTCAAGTTAGAA[C/T]TGTGACGTTAGTGAT	57674
rs190182794	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80266863	TTCTTGAGGAAGGCA[C/T]GTTGAAAGCTGAGAT	57674
rs190186533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301853	ATATTTATCGTAACA[C/T]TCAATAGCCATAATA	57674
rs190190592	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330210	TTCTGGGTTATTCAC[C/T]GTTTTGTTTTGGAGG	57674
rs190243139	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80281233	CCACACACACCCCAC[A/T]CACACACACCTCAAC	57674
rs190314125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323701	CTCAGATGATCAACC[C/T]GCCTTGACCTCCCAG	57674
rs190324494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384014	GCTTTTACGTAGTAT[A/G]ATCATTCTTAACAGA	57674
rs190333263	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360008	AGATCTTATCTTGTG[C/T]TTTGAGTGACGTCTC	57674
rs190340228	snp	A/G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355666	TGGACGGGAATGGGG[A/G/T]CTTACAGGGGGAAGA	57674
rs190350636	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF213, LOC100294362	GRCh38.p7	17:80360404	AGGAGTGAGAGGCCC[C/T]GGCGGGACCAGAAAC	57674
rs190351645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369289	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	57674
rs190390884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261993	TGTACTCCAGCCTGG[A/G]TGAAACTGTCAAACA	57674
rs190408411	snp	G/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286805	TGACCTGATCCACAC[G/T]CACCCCTGAGTACTG	57674
rs190417594	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80299417	GAACTCTAAACCATT[C/T]ATACCTTTGCATAAT	57674
rs190423597	snp	C/G	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394732	ACCTTGAGCAGCGCC[C/G]GCAGGAGGCACGGAA	57674
rs190425923	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80326114	CAGATGTGAGCCACT[A/G]TGCCCAGCAGTTTAT	57674
rs190428683	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80306886	AGGCGTCTCATGTGA[C/T]GCACTTCGTAGCTGC	57674
rs190454814	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80324473	TGGGGCTGGATAAGG[C/T]TTTCTTTTATCCTTT	57674
rs190455678	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387209	CCTCTGGGCTCAAGC[A/G]ATCCTCTCACATCAG	57674
rs190492035	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397510	AGATTACAGACATTA[C/T]ATAGAAAAGCACCGT	57674
rs190522152	snp	G/T	0.0146672	0.084371	intron-variant	RNF213	GRCh38.p7	17:80270150	TGGCAGCTCGTGCCC[G/T]GCGCATGCCTTGCTA	57674
rs190529817	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80306530	ACTAGATAACTAAAC[A/G]TGGAAAGCTCAGGAT	57674
rs190532901	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80286204	GGGGTTGGTGTCGGA[C/T]GCAGGCCGGTGTTGG	57674
rs190561125	snp	C/T	0.0154538	0.0865337	intron-variant	RNF213	GRCh38.p7	17:80305429	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	57674
rs190562417	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363485	GACGCTTCTCACATC[A/C]TAGACAATGAAAGTT	57674
rs190565503	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366579	CATTTTTGAATTGGG[C/T]TGTTGATTAACAAAG	57674
rs190567403	snp	C/T	0.000164807	0.00907614	synonymous-codon	RNF213	GRCh38.p7	17:80345553	TAAAATCCTTGCCAT[C/T]GAGATGCGGTTCCGG	57674
rs190589678	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80311629	CCTGGCCCTTCCCAG[A/G]TATAGTGACGCTGTG	57674
rs190615385	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350558	TGGGATTAGGGAAAC[C/T]GAAGAGAGACAAAAA	57674
rs190629194	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382724	AGTTCTGTTCTTTCA[A/G]TAATTTTTTTCAAAA	57674
rs190658929	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80280084	CTTCAAGGCAGGCAT[A/G]CTCTTTCCTCTGTGG	57674
rs190662574	snp	A/C	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398420	TATGGAGTACTATGA[A/C]ACCAGGAAAACTTAA	57674
rs190670971	snp	A/G	0.0189856	0.0955633	intron-variant	RNF213	GRCh38.p7	17:80318675	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	57674
rs190681727	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80274513	GGGCTGGCTTTCTGT[C/T]TGTCGTTCCTTGTAG	57674
rs190695019	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363883	ATGAGAAGACGGGCA[A/G]GTGCTCCTGCCATGG	57674
rs190700835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381894	CGTGTCTAGGGAAGG[C/T]GATGCCTGGGGCTGG	57674
rs190798563	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80349436	AAGCATGAGTCGTAC[C/T]ATAACAGGAAATGGC	57674
rs190809282	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80277448	ACTAAAAATACAAAA[A/G]GTAGCCGGGTGTGGT	57674
rs190821352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298204	CTCTGCTCAGCCACG[C/T]GCGGTGCTCCTCTTG	57674
rs190831783	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317007	TTCTAGAAAGCCAAC[C/T]TGGGCTGCTGTGACC	57674
rs190849001	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331318	CCACTGGTTCAGCTC[A/G]TTTTCAACTTCTAAA	57674
rs190856573	snp	C/T	0.000316232	0.0125704	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385607	ACAAACTGAGGAGAT[C/T]GCTTGAGACGAACGG	57674
rs190870623	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364361	TCTCTTCTCCCGTCT[C/G]CCTCCTCGTTTCACC	57674
rs190873832	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315568	TGGAGGTGATGGTGG[A/T]GGTAATGGAGGTGAT	57674
rs190989652	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372429	ATTCTTCTATCCTTC[C/T]TTCTCCACAGTCACA	57674
rs191077627	snp	A/C/T	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390058	AAGCGGATCTGAGCC[A/C/T]GGAAAATGCTAAGCT	57674
rs191078009	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357772	TGCCCAGGAGTTTGA[G/T]ACCAGCCAGCTAGGG	57674
rs191079940	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80331814	TATGATGCTTTCTTT[A/G]TCATGAATATTGGTT	57674
rs191093906	snp	C/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80290888	CATCTCAGCTCACTG[C/G]AGCCTCCGCCTCCTG	57674
rs191250827	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282437	GGAGTCTCACTCTGT[C/T]GCCCAGGCCGGAGTG	57674
rs191254637	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80274911	TGTTGGGGGTGTGTG[A/T]GTGGGGTGTGAGTGG	57674
rs191258719	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302969	TAACCCTTCTAAGCA[A/C]AATAGATTAATTTAT	57674
rs191261012	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320681	AGGTGTGAGCCACCG[C/T]GCCCGGCCGAGCATA	57674
rs191267060	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80342848	GTCTTAAGGGATGCC[C/T]AGGCTGGAGTGTAGT	57674
rs191334064	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270783	GCTCAGCAAGAGAAA[C/T]GTGCTGGGTCACCGT	57674
rs191344023	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297150	TAGGCTCAACCCTTA[A/C]GTTTAAAAAGTTGTT	57674
rs191346414	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80274173	GCTTTGAAGCTTTGG[A/G]TGTGGGGTGGGTGCT	57674
rs191357734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335657	AAATTGCTCAGGAAC[A/G]GCAAGATATCGTTTA	57674
rs191358537	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391610	AGAGCTCTTTGCATA[C/G]AACAGGGGTTCATCT	57674
rs191371799	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367514	GAGGAGACCTTAAAA[A/G/T]AAAAAGAAGAGGGAA	57674
rs191379510	snp	C/T	0.00020643	0.0101574	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358529	ACTATCAGAACACAG[C/T]AGGACCCTAATATGC	57674
rs191388106	snp	C/T	0.00294987	0.0382914	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373048	GGAGAACGACTGGCA[C/T]CGGGTGTACCTGGTG	57674
rs191393457	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80278130	GAAGAGGAGACTGCC[A/G]GAGCCAGGGGTCATT	57674
rs191399657	snp	C/G			synonymous-codon	RNF213	GRCh38.p7	17:80346060	TCTGCCCCCGAGCCT[C/G]ATTCCTCTGGTGTGG	57674
rs191401535	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317538	TTTTTCCTGACCCCT[G/T]CGTTGGACTTGCGAC	57674
rs191412255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375979	AATTTTTTTATCTAG[A/G]ATAGAGGTTCTCAAC	57674
rs191412540	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80274750	TCTGTGGGGGGTGAG[C/T]GGGGTGAGTGTGGGG	57674
rs191434862	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370597	GCCAGTTTCATTTTA[A/G]TTTTACTAAATCTTG	57674
rs191445090	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388751	CAGTGTGTTTCCCTC[C/T]GTGTTAGGCCTACTC	57674
rs191459642	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277241	AACACAGATTAGTGG[A/T]TGGCTGGGAGGAGTG	57674
rs191484948	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF213	GRCh38.p7	17:80260892	GCAGGCGGCGAGCTC[C/G]GGGGCCGCAGGTGCG	57674
rs191491971	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299135	AACAAATGATGTGTT[A/C]TTTATTCTGGTTTAC	57674
rs191495962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279900	GGAGCTTCATACCTT[A/G]AAGAGTGATGCTTGT	57674
rs191511942	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80318572	ATATGAGAGTTTTAT[A/G]TGTAACTTTTTTTTT	57674
rs191517461	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395889	ACTTTGTCTGCCCTG[C/T]GCCAGCCTCACCTCA	57674
rs191517878	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80337486	AAGCGTGGGGAGAAG[G/T]CTCTGCAGCGAGGCA	57674
rs191523834	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356174	ACCCAGCTACTTTTG[A/G]TATTTTTAGTAGAGG	57674
rs191530492	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379381	AAGTGTCACTCTGGG[A/C]ATAAAGCTTAAATTG	57674
rs191579451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316494	GCAGAAAAGAGACGT[A/G]ATAAGTAAGTACAGC	57674
rs191590325	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391197	ATCTCATTTTCAGTT[G/T]TATTTCCCCATTTAC	57674
rs191599810	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355600	AATGGGGGCTTACAG[A/G]GGAAGAAGCGGGGTG	57674
rs191623236	snp	C/G	0.000399281	0.0141238	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385169	TCAGCAAGCACAGCT[C/G]AGGTGTGGCTCTGCT	57674
rs191633525	snp	A/C/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320129	ACAGTTAATGACAGA[A/C/G]CATTTTCATCACTTC	57674
rs191648285	snp	C/T	0.000443845	0.0148905	intron-variant	RNF213	GRCh38.p7	17:80298562	TGAATCTGGGAAGAC[C/T]GACTCCTACATTGTG	57674
rs191655687	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357956	TTGTGTCACTACACC[A/G]CAGTTGGCGTGACAG	57674
rs191657226	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336572	AAGCAGGATACAAAA[C/T]TACATGACACATAGT	57674
rs191691062	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394237	AGATTCTTCTGATCT[C/G]ACATTTTGAAATTGT	57674
rs191818317	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328598	TTAAAATTTTTTTTT[A/T]AATTTGCATTTGCTG	57674
rs191818551	snp	A/G	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80348687	GCTTAGAGGCAGCGG[A/G]GAGCGGTGCAGACCA	57674
rs191830582	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362454	ACATCCAGGAAACAT[C/T]TGAAAAATTGCTTAG	57674
rs191881234	snp	C/T	0.00835572	0.0641442	intron-variant	RNF213	GRCh38.p7	17:80285827	AGGTGCCTGCCACCA[C/T]GCCCAGCTAATTTTT	57674
rs191897121	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80272191	TGGGAGGCCGAGGCA[G/T]GAGAATTGCTTGAAC	57674
rs191911212	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80308507	CCTCCTGAGTCCCTC[C/T]TAAGGCTCCTCCCGA	57674
rs191928060	snp	A/C/T	0.00438476	0.0466401	intron-variant	RNF213	GRCh38.p7	17:80327526	GTATACTGAAGGGGA[A/C/T]GTGGGTTTTAACCTG	57674
rs191936761	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259334	TTAGCCAGGCTTGGT[A/G]GCGGGCGCTTGTAAT	57674
rs191944878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341956	GGACTACAGGCACAC[A/G]CCACCACACCTGACT	57674
rs191959047	snp	C/T	0.000843208	0.0205157	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372752	AAGTCTTCTCTGCCT[C/T]GCTTTCCTTTGGGTT	57674
rs191994788	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80266011	TGGAGACATTGAGTT[C/T]CAAATGATATAAAGT	57674
rs192044523	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80348455	GTAGGTCCAGTTAAC[C/T]AGGTGCTGAGTGCCT	57674
rs192056308	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315835	GTGGTGGTGATGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs192057296	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364822	GGGCTGACGCAGGGA[A/C]CATGCTTGTGAAACC	57674
rs192098846	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383504	GGGAGACATACATCT[A/G]TAAACAAACAACACT	57674
rs192106754	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80300822	CTCCCAAAGTGCTGG[A/G]ATTGCATGTGTGAGC	57674
rs192121881	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80341054	ATGATCTGCCCTCCT[C/T]GGCCTCCCAAAGTAC	57674
rs192145542	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371234	TTGCAACTAACCTCT[A/G]GACATGACCATTTAT	57674
rs192152984	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388858	TCAGCAAGTTTTCTT[A/G]TAGAGTAAAAGCAGA	57674
rs192173389	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332551	CACCAGGCTGTCCAC[A/G]CAGCCAAGGTCATCT	57674
rs192180292	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352627	CCCCTCACTAACTGT[C/G]ATACAGCAAATACAA	57674
rs192188074	snp	A/G	0.0618563	0.164627	intron-variant	RNF213	GRCh38.p7	17:80322182	TTTTTTTTTTTTGAG[A/G]AAAGGTCTCGCTTTG	57674
rs192192514	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365487	CACCCCGTGGCCTGG[C/T]GTCACAGCCTGTGGG	57674
rs192196012	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270010	GGACATAAAATAGCA[C/T]GAAGTTTCCTCACCC	57674
rs192281057	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353151	TGGCACTAGGAGCAG[A/G]GCCACCGTGTTTCGT	57674
rs192299839	snp	A/C	3.29457e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383794	TTCCTGCCCCACCTG[A/C]CCCGGAAAAGTGTGG	57674
rs192384069	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326640	CCAGAATGTCCTATG[C/G]TTGGAATCTTATAGG	57674
rs192398972	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361075	AATTTACTTGGACCC[A/G]GGGGTTCCTGAAGCA	57674
rs192426295	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383333	AGTGTTTTTCTCTCC[A/G]TTACTTTTTACAGCA	57674
rs192457524	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80281762	TCGGTTCCAGGACCG[C/T]GGAGGACGCCAAAAT	57674
rs192477067	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319664	AACACTTGCTCAGTA[C/G]GTGTGCGGGAAGAGA	57674
rs192518540	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80267131	CTGAGGCACAAGAAT[A/T]GCTTGAACCCAGGAG	57674
rs192551143	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80275114	TGTGTTGGGTGTGTG[C/T]GTGTTGGGTGTGTGT	57674
rs192625705	snp	A/T	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373601	GTGGCCTTTGCTTTC[A/T]GCGAATTAAACGTAG	57674
rs192635803	snp	G/T	0.00874735	0.0655527	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392469	GCCAGCACAGGGCTT[G/T]CTCCGTGGGCTTCTG	57674
rs192686176	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80333038	TTTCTGTTAGAGTTA[A/C]GAGGTGACTCTTTTG	57674
rs192689761	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80291512	TCAGGCATGGGCCAC[A/T]GAACCCAGCCTTGCC	57674
rs192699797	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80312652	TCTAAGGAACAGGCC[C/T]GGGAGTCTGCAGGGC	57674
rs192703243	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366317	TTTATGCAGAGGCAC[C/T]GTATTGTTTTCCACG	57674
rs192741612	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307509	CTGGGATTACAGGCG[C/T]ACCCCACCACGCCCA	57674
rs192751125	snp	A/G/T	1.65414e-05	0.00287583	synonymous-codon, missense	RNF213	GRCh38.p7	17:80347365	GGCCAAGTGCTCAGA[A/G/T]GAAGTCAGCCCCATG	57674
rs192757873	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80337313	CACTCCTCCACAGAT[A/G]TAAGTCAAGTGCCCC	57674
rs192762149	snp	C/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377240	CATTTTGGGAGAAGG[C/G]AGGGACTGGGAACCA	57674
rs192766023	snp	G/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80309411	TGGGAGGGAGGCAGG[G/T]AGTTAATGTGTGGCC	57674
rs192767810	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370252	TCCTAGATGTCTCCT[A/G]AGTTTCTATTCCCCT	57674
rs192799555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272531	AGTAAACAAGCCTCT[C/T]AAGAGTAAACCCATG	57674
rs192803517	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298838	AAAAAAATTAGCCAG[A/G]TGTGGTGGCATGTGC	57674
rs192889985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378274	TTATTAGCCCTCAGA[A/G]GAGGTGTGGTCCAGA	57674
rs192908330	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359153	AGGCCTGATGATGTG[A/C]GGCTCAGGCTCAGCT	57674
rs192938221	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393007	TTTTTTGAGACAGGA[A/T]CTCACTGTGGCCCAG	57674
rs192962862	snp	C/G	0.00159617	0.0282053	intron-variant, missense	RNF213	GRCh38.p7	17:80288864	TGGGGATATAGCCAT[C/G]ATTCAGACAAAGCTC	57674
rs192964319	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318057	CCCTGAAGTCAGGAC[A/G]TCTTTCCGAAGTTAA	57674
rs192973062	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355840	GAAGAAGCGGGGTGA[A/C]CGGGAATGGGGACTT	57674
rs192980468	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387894	CAGCTGCAGTCATAT[A/C]TACTGTACTTATGTA	57674
rs193069321	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395694	CCTGAGTCCACTTGC[A/G]GGGTAAGAGATAAAC	57674
rs193072671	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287585	CAGCCCGGCCGTGAC[C/T]GTGCCGAGTGTGGCG	57674
rs193127589	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80303432	CCAAAGACTGGGGAC[A/G]GCAGAAAAAATGAGG	57674
rs193151938	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80267527	TGGAGAGAGTTTGCA[A/G]TGTCTGGAGAGGTCA	57674
rs193159395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374240	GGTAGCGCTGCCGTC[A/G]GCAGGCATTCCCTGC	57674
rs193169015	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274744	GGGGTGTCTGTGGGG[A/G]GTGAGTGGGGTGAGT	57674
rs193240978	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80272028	GGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG	57674
rs193282584	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321468	GCTGATACAAACATT[A/C]GTGTACATATTTATG	57674
rs193286572	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358875	GATGGCGCCACTGCA[C/T]TCCAGCCTGGTGACA	57674
rs193300182	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80283112	TAAAATTATAAATAC[C/T]GCTATGGTTATGTAG	57674
rs199503043	in-del	-/TA	0.167809	0.236103	intron-variant	RNF213	GRCh38.p7	17:80342733	TATGTATATATATAT[-/TA]TATATATATATTGTA	57674
rs199523492	snp	A/G	0.000466955	0.0152728	missense	RNF213	GRCh38.p7	17:80346604	GTCTTCATGATGGTC[A/G]TCTGCATCGAGCTGA	57674
rs199525656	snp	G/T	0.000148406	0.00861283	intron-variant, missense	RNF213	GRCh38.p7	17:80319400	ATGAAGCACCCGCTG[G/T]GTCTCAGCTCCTCCG	57674
rs199557416	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80324570	AGAAACTTTGAACCT[A/T]AAGGAAGAAAAATAT	57674
rs199564196	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80281603	CTGCCAACACACACA[C/G]CCAACTCACACCACT	57674
rs199572015	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311367	GTGCAGCCTCTGAGC[A/G]GTCATTCAGTTTGTT	57674
rs199587381	in-del	-/TATC			intron-variant	RNF213	GRCh38.p7	17:80269371	CCCTATCTATCTATC[-/TATC]CACCTATCCATCTGT	57674
rs199588321	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80338649	TTTTTTTTCCCAATT[A/T]AAAAAAAAAGATAAT	57674
rs199590606	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314633	GGTGGTGGAGGTACT[A/G]GAGGTGATGGCGGTC	57674
rs199610554	in-del	-/AGC			intron-variant	RNF213	GRCh38.p7	17:80315591	AGGTGATGGTGGTGG[-/AGC]TGGTGGTGGTACTGG	57674
rs199613694	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292299	ATGTTGGACCTTGAC[C/T]TCAGGTGATCTGCCC	57674
rs199628684	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368583	GATTACAGGCATGCA[C/T]CACCATGCCCGGCTA	57674
rs199649793	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386989	AAGCAGCACCTCACC[C/G]TGCAGTCTGGTCTGT	57674
rs199660561	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80309087	TGAAGCCATCTGCAG[C/T]AGCACAAAGCTACTT	57674
rs199681539	in-del	-/GGA			intron-variant	RNF213	GRCh38.p7	17:80315220	GGTGATGGTGGTGGT[-/GGA]GGTGGTGGAGGTACT	57674
rs199684832	snp	C/T	0.000263904	0.011484	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354550	AGCCTGCAACCAGGA[C/T]GCTCTCCAGGAGGCG	57674
rs199703548	snp	C/T	0.00199792	0.0315431	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383957	ACTGTGGCTCCCTCC[C/T]TCTTTCGGTGCAGAG	57674
rs199729731	snp	C/G/T	4.94176e-05	0.00497059	missense	RNF213	GRCh38.p7	17:80291683	TGCATTTCCAAGAAG[C/G/T]ACCTAGATAAATACA	57674
rs199745423	snp	A/G	4.94173e-05	0.00497053	missense	RNF213	GRCh38.p7	17:80345178	GCACATGGTCACCAT[A/G]GATGGGGTTAGGGAA	57674
rs199753442	snp	C/T	0.00199792	0.0315431	missense	RNF213	GRCh38.p7	17:80347837	ATCCCCCTCATTAAC[C/T]GGCTGGAGAAGCACT	57674
rs199769375	in-del	-/GT	0.0228947	0.104514	intron-variant	RNF213	GRCh38.p7	17:80275122	GTGTGTGCGTGTTGG[-/GT]GTGTGTGAGTGGTGT	57674
rs199769742	snp	C/T	0.000151109	0.00869091	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360139	CAACAACGTCCCTTT[C/T]AGCTGGAAAATCAAG	57674
rs199777836	snp	C/T	0.000247131	0.0111133	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288612	TTTGTCACCTTGGCT[C/T]TGGTGTTTGGGGTCT	57674
rs199787553	snp	C/T	8.25117e-05	0.00642254	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386679	CTGAGCGCTGTCTTT[C/T]TGCCCCTCAGCTATT	57674
rs199793046	snp	C/T	0.000132972	0.00815282	missense	RNF213	GRCh38.p7	17:80343321	ACCTGGACGTGACCT[C/T]CTCAGTAAGTGCCCT	57674
rs199795186	snp	A/C/G	8.24823e-05	0.00642146	missense	RNF213	GRCh38.p7	17:80313153	GCCTCATTCACATAC[A/C/G]TCAAGGAAATTGAGG	57674
rs199799029	snp	A/G	1.65119e-05	0.00287327	missense	RNF213	GRCh38.p7	17:80348134	GCTACGCCCGATGCC[A/G]TGGTCCGGCTGAGCG	57674
rs199809054	snp	C/T	8.24368e-05	0.00641963	intron-variant	RNF213	GRCh38.p7	17:80319173	GCTCTGAAACCACCC[C/T]CCTTTGATTTTTGCA	57674
rs199817210	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80274884	GTGAGTGGTGTGAAT[C/G]GGATGTGTGTGTGTT	57674
rs199835842	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80349386	TTGCTGACATCTGGG[C/G]GAAGGGGACAGCACC	57674
rs199836357	in-del	-/AAG			intron-variant	RNF213	GRCh38.p7	17:80314811	GTGATGGTGGTGGTG[-/AAG]GTGATGGTGGAGGTA	57674
rs199840787	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377451	ACAAAAAAAAAAAAA[A/T]CAAGGAAAATAGAAA	57674
rs199854651	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80307546	TTTTGTGTGTTGGTT[G/T]GTTTGTTTGTTTGTT	57674
rs199868778	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80325677	TGCTGTCTGATTTCC[A/C]CCCAGCCCCCCGCGC	57674
rs199887580	snp	A/G	9.8912e-05	0.0070318	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380938	TCTTCCTCCTTATCC[A/G]GCTACTCACTCACTT	57674
rs199905492	in-del	-/ATTT			intron-variant	RNF213	GRCh38.p7	17:80276116	TTTATTTATTTATTT[-/ATTT]TTGAGATGGAGTTTC	57674
rs199933849	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315729	GATGGTGGAGGTACT[A/G]GAGGTGATGGTGGTG	57674
rs199939295	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80294343	CTCACTTGCTAGTGG[C/G]GGGATGCGGTTTCTG	57674
rs199975233	snp	C/T	0.000300145	0.0122467	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363640	CCGCAATGGCCTGCA[C/T]GGAGATGCTGACAAG	57674
rs199976159	snp	A/G	6.7784e-05	0.00582129	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288217	TCCCAGGAGGGGACC[A/G]GTCCCCCCACCTCTG	57674
rs199980217	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375554	AAAGAAAAAAAAAAA[A/G]AATTAGCCGGACATG	57674
rs199998736	in-del	-/AG			intron-variant	RNF213	GRCh38.p7	17:80274834	TGTCTGTGGGGGGTG[-/AG]TGGGGGGTGAGTGGG	57674
rs200004017	snp	A/G	8.40033e-05	0.00648032	intron-variant	RNF213	GRCh38.p7	17:80295522	GGTGAATTCAAGTCC[A/G]TGGTTCATGCATCTT	57674
rs200011985	snp	C/T	4.94173e-05	0.00497053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389996	TAATGCTTCATTTGC[C/T]CTTCCGTCGTTTTAG	57674
rs200017187	in-del	-/CTCCTA			intron-variant	RNF213	GRCh38.p7	17:80316293	TTCATGTGTTTCAAC[-/CTCCTA]GTGTCCCTGCCAAAA	57674
rs200034624	snp	A/G	3.34594e-05	0.00409006	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373083	AGCTCAGCAGCCAGC[A/G]GGGGATGGAGTTCGT	57674
rs200035976	in-del	-/AC			intron-variant	RNF213	GRCh38.p7	17:80301464	CAAGTGAACAGAAAA[-/AC]TCAGATCTAAAAATG	57674
rs200065117	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359603	GAAAGAAAGAGCGAG[A/C]GAAAGAGAGAAAGAA	57674
rs200069509	in-del	-/C	0.0182019	0.0936463	intron-variant	RNF213	GRCh38.p7	17:80316251	AGCGAGACCCTGTCT[-/C]TTAAAATATTTTTTT	57674
rs200079469	snp	C/T	0.00299544	0.0385843	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371996	TGGAGGTAAGTGAAC[C/T]CTCTCTTCCCTGAAT	57674
rs200091899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306237	CTTTTCTCCGTCCCT[A/G]TTTCTCTTATGCAGG	57674
rs200093086	snp	A/C/G/T	0.000131841	0.00811823	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288777	CTCCTTCCTGCCTGC[A/C/G/T]GGCTCCAGGAGGCCC	57674
rs200099417	snp	C/T	0.000543922	0.0164823	missense	RNF213	GRCh38.p7	17:80345810	ATGAAGCCAACACAA[C/T]GGAAGCTATAAGCTG	57674
rs200107943	snp	A/G	0.00033274	0.0128942	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390174	CAAACCCAAACCGAG[A/G]AGCGCTTCCGCCCTC	57674
rs200111823	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80290415	TGCTTGTGTGTGTGC[A/G]TGTGTGCGAGTGTGC	57674
rs200131626	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380765	CTCACTCCAAGTGCT[A/G]AGAAAGTGCAGCGTG	57674
rs200133294	snp	C/T	8.23621e-05	0.00641672	missense	RNF213	GRCh38.p7	17:80346191	TGATCACAGAAGTCC[C/T]CTGCGCCTCTCAGGG	57674
rs200144340	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313593	GAGGTGGTGGAGGTG[A/G]TGGTGGTGGTGGAGG	57674
rs200150061	in-del	-/ACTGGA			intron-variant	RNF213	GRCh38.p7	17:80315666	GGTGATGGTGGTGGT[-/ACTGGA]GGTGATGGTGGTGGT	57674
rs200162965	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80309042	GGAGGCCTTGTCACC[A/G]TCCTACCTGACTGTG	57674
rs200168435	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267314	GGCATGGTGGCGTGT[A/G]CCTGTAGTCCCAGCT	57674
rs200168617	snp	G/T	0.000131852	0.00811842	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389291	TGAGCACAGCTGGTG[G/T]GGATCCAAACATGCA	57674
rs200178604	snp	A/G/T	0.000577804	0.0169875	intron-variant	RNF213	GRCh38.p7	17:80295025	GGCTTGCCACCAGCT[A/G/T]CTCTACCTGCTGGGC	57674
rs200188581	snp	A/C/G	0.000178559	0.00944738	synonymous-codon, missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287973	CAGCCAAGCCCAGCA[A/C/G]AGTGGCCCCACTGGC	57674
rs200197408	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281339	ACTCACACACGCCCC[A/C]ACACACACACCCCAC	57674
rs200208573	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377835	GGTTTGAGGGGTGGC[A/G]TGCACTCCTGGGTTG	57674
rs200216180	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315848	TGATGGTGGTGGTGG[A/T]GGTGGTGGAGGTGAT	57674
rs200217989	snp	C/T	0.000214729	0.0103595	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354564	ACGCTCTCCAGGAGG[C/T]GGGCACATTCAGGTA	57674
rs200219786	snp	A/T	0.0885008	0.190835	intron-variant	RNF213	GRCh38.p7	17:80276093	TTTATTTATTTTTTG[A/T]TTTATTTATTTATTT	57674
rs200227011	snp	A/G	0.00199792	0.0315431	missense	RNF213	GRCh38.p7	17:80347664	TGCAGAACCTCTACG[A/G]GAGCCTCTACGACGC	57674
rs200232995	in-del	-/ACGTGA			intron-variant	RNF213	GRCh38.p7	17:80315184	AGGTGATGGTGGTGG[-/ACGTGA]TGGTGGAGGTAATGG	57674
rs200234822	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338880	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	57674
rs200237197	snp	A/G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80328589	GAGAAGGCTTTAAAA[A/G/T]TTTTTTTTTAATTTG	57674
rs200247672	snp	C/G	0.000709495	0.0188214	missense	RNF213	GRCh38.p7	17:80313075	GTCTTCCAAGGGACC[C/G]TTGCTGCTACGAAAA	57674
rs200256523	snp	A/G	0.000519007	0.0161007	missense	RNF213	GRCh38.p7	17:80346691	ATCGTGGCAGACGCC[A/G]TGCAGGGCCCGGCTG	57674
rs200282413	snp	C/T	0.00199802	0.0315439	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374541	CCGTGATGCTGTGGC[C/T]AAAGCTGTCCTCGAG	57674
rs200285743	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80281619	CCAACTCACACCACT[-/CA]CACACACCCCCAACA	57674
rs200299053	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314859	GTGGTGGTGGTGGTG[A/G]TGGAGGTAATGGAGG	57674
rs200300662	in-del	-/GA			intron-variant	RNF213	GRCh38.p7	17:80274910	GTGTTGGGGGTGTGT[-/GA]GTGGGGTGTGAGTGG	57674
rs200306837	snp	A/C/G	0.000527226	0.016228	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393426	TCAGTTCCCAGAAGA[A/C/G]ATACTGCTCGCCAGC	57674
rs200314393	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80302275	AGCTGGAAGAGTGGA[G/T]TTTGAATGTTTCCAA	57674
rs200316494	snp	A/G	0.000494266	0.0157127	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374487	CCACCCAGGCCAGAT[A/G]GATAGGTACCTGGTG	57674
rs200327542	snp	A/G	0.00653684	0.0567952	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381612	GCAGCAGCACATCCT[A/G]AAGGACCTGGAGCAG	57674
rs200339444	in-del	-/TGA			intron-variant	RNF213	GRCh38.p7	17:80314400	TGGAGGTAATGGAGG[-/TGA]TGGTGGTGGTGGTGG	57674
rs200390819	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80284380	AAAAAAAACAAAAAC[A/C]AAAACAAAACAAAAA	57674
rs200400003	snp	A/G	0.000116404	0.00762813	missense	RNF213	GRCh38.p7	17:80273253	CAGATTCTGAGAACA[A/G]TAACTCCACAATGGC	57674
rs200405934	in-del	-/GT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359502	ACTCTAGCCTGGGTG[-/GT]GACAGAGTGAGACTC	57674
rs200418091	snp	C/T	0.000214495	0.0103538	intron-variant	RNF213	GRCh38.p7	17:80319144	CATAGAGCACTGGAG[C/T]GCTGCATCCGAAAGC	57674
rs200418522	snp	C/G/T	0.000466651	0.0152679	missense, synonymous-codon	RNF213	GRCh38.p7	17:80346913	ATGCCCCTGAAGACT[C/G/T]TGCACCCGCTGCTGG	57674
rs200427673	in-del	-/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80311467	CTTCAGCAGTGCCTG[-/T]TTTCGTTTTCTGTCG	57674
rs200435901	snp	A/C/T	0.000131777	0.00811619	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376364	CCTCCTGATATCAGC[A/C/T]GTTTTGCAACATCGC	57674
rs200437340	snp	C/T	0.000406497	0.0142507	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288234	TCCCCCCACCTCTGC[C/T]GGTGAAGGCCATTCT	57674
rs200441387	in-del	-/GCGGG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355645	CTTACAGGGGAAGAA[-/GCGGG]GTGGACGGGAATGGG	57674
rs200460613	snp	A/G/T			intron-variant	RNF213	GRCh38.p7	17:80314121	GTGATGGTGGTGGTG[A/G/T]AGGTGATGGTGGAGG	57674
rs200483027	snp	C/T	0.0002344	0.0108234	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354625	AATCTGGTGGCAGCA[C/T]GGGGACCTGCCTGCA	57674
rs200484293	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355673	GAATGGGGGCTTACA[-/G]GGGGAAGAAGCGGGG	57674
rs200507140	snp	A/G	0.000115334	0.00759299	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379650	GAACAGAGCATCTGC[A/G]TTGACTGCCATGCGC	57674
rs200514569	in-del	-/T	0.00358779	0.0422022	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259691	AATTTTTTTAAATGA[-/T]TTTTTTTTGTAGAGA	57674
rs200515308	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80270111	GCGTGAATGTGTGCG[-/CA]CACACACACACGTTA	57674
rs200537097	snp	A/C	6.58924e-05	0.0057395	missense	RNF213	GRCh38.p7	17:80294865	GGACAGCACCTTCAG[A/C]ATCCTGCAGACCTGG	57674
rs200546205	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80313137	GCTCACATCTTCAGG[C/T]GCCTCATTCACATAC	57674
rs200587481	snp	C/G	0.00199806	0.0315442	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372611	CTTAAGGCATATTCT[C/G]CAGCAAGCCGGGGCC	57674
rs200597493	in-del	-/TGA			intron-variant	RNF213	GRCh38.p7	17:80313789	AGGTGATGGTGGTGG[-/TGA]AGGTGATGGTGGAGG	57674
rs200625556	snp	C/T	0.00161452	0.0283664	intron-variant, missense	RNF213	GRCh38.p7	17:80319395	GGGCTATGAAGCACC[C/T]GCTGGGTCTCAGCTC	57674
rs200635394	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281244	CCACTCACACACACC[C/T]CAACACACATACCCC	57674
rs200656035	snp	C/T	0.00199795	0.0315433	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376587	TTCACTGGAACACCC[C/T]CCAGAGCTTGTCACT	57674
rs200660669	snp	A/G	0.0109394	0.073144	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361682	CCCTGGAGGCAGGGG[A/G]GCGCCATGACTTAGA	57674
rs200673034	in-del	-/AGAC	0.0295035	0.117819	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382276	AAGAAAAGGTCTGTA[-/AGAC]AACTTAGTAAAATGG	57674
rs200674629	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315662	TGGAGGTGATGGTGG[A/T]GGTACTGGAGGTGAT	57674
rs200680083	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80268380	AAAAAAAAAAAAAAA[-/G]GCAGTACTGCATCCC	57674
rs200689297	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333350	CAGGCGTGAGCCACC[A/G]TGCCCGGCTGAGTCT	57674
rs200704623	snp	C/T	0.00199806	0.0315443	synonymous-codon	RNF213	GRCh38.p7	17:80347935	GGAGAAGTTCATCAA[C/T]GTCAAAGCACATCAT	57674
rs200715267	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367128	CCTAAGGTATCATGA[-/A]GAGAATGAGTTGCAG	57674
rs200724769	snp	C/T	4.94401e-05	0.00497168	missense	RNF213	GRCh38.p7	17:80345401	TACCAGGGCCTGCTG[C/T]TCCAGAGGGTGCCCT	57674
rs200731403	snp	G/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80294870	GCACCTTCAGCATCC[G/T]GCAGACCTGGGACAC	57674
rs200732556	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281398	CCCACTCACACCACT[C/T]ACACACCCCCAAGAC	57674
rs200760856	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355378	GGAATGGGAGCTTAC[A/G]GGGGAAGAAGCGGGG	57674
rs200771615	in-del	-/GGA			intron-variant	RNF213	GRCh38.p7	17:80315737	GGTACTGGAGGTGAT[-/GGA]GGTGGTGGTGGTGGA	57674
rs200772672	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80281366	CCACTCACACACACC[-/T]CAACACACACACACA	57674
rs200773996	snp	C/T	0.000660153	0.018156	intron-variant	RNF213	GRCh38.p7	17:80313181	AGGTAGGCATTTGGC[C/T]GAAGGCTTCTGGGTA	57674
rs200776945	snp	C/T	0.0013187	0.0256439	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385215	CTGTCCCGCATTTGG[C/T]GGTTCGAAAGGATCA	57674
rs200778688	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80325678	GCTGTCTGATTTCCC[G/T]CCAGCCCCCCGCGCC	57674
rs200787670	in-del	-/GGG			intron-variant	RNF213	GRCh38.p7	17:80274840	TGGGGGGTGAGTGGG[-/GGG]TGAGTGGGGTGTGTG	57674
rs200804939	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390721	ATATATTCTAATTTT[A/T]TAACAAGTAGACTAT	57674
rs200810647	snp	A/G	0.000181185	0.00951628	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377749	GCCAATGTGTGTCCT[A/G]TTCTCTTCACAGCTT	57674
rs200832992	snp	C/T	0.000133253	0.00816143	missense	RNF213	GRCh38.p7	17:80298518	AACAAATGCTAGATA[C/T]GTAAGTCGTAGAGTT	57674
rs200834610	in-del	-/GT	0.140919	0.224948	intron-variant	RNF213	GRCh38.p7	17:80275135	GGGTGTGTGTGAGTG[-/GT]GTGTGTGTGTTGGGA	57674
rs200848848	in-del	-/ATCC			intron-variant	RNF213	GRCh38.p7	17:80269409	TCTGTCCTATCATCT[-/ATCC]ATCCATCCATCCATT	57674
rs200852207	snp	A/T	4.94222e-05	0.00497078	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375804	AGCCTACTTCCTGTT[A/T]ACACTGTTTAGAGAG	57674
rs200858897	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359606	AGAAAGAGCGAGAGA[A/G]AGAGAGAAAGAAAGT	57674
rs200865029	snp	A/G	0.00026534	0.0115152	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369834	AGACTCCTGTCATCC[A/G]CTCAGTGATACTGAA	57674
rs200866115	snp	G/T	0.0310518	0.120672	intron-variant	RNF213	GRCh38.p7	17:80307863	CCGTCTGTTTTTTTT[G/T]TTTTTTTTTTTTTAA	57674
rs200875331	snp	A/G	0.000153988	0.00877328	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361877	CGTGTGTCAACGGAG[A/G]AGGAATTAAAGGTAG	57674
rs200877731	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80313466	TGGTGGTAGAGGTGA[-/TGG]TGGTGGTGGAGGTGA	57674
rs200889339	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80275146	AGTGGTGTGTGTGTG[-/TT]GGGAGTGTGTGTGGG	57674
rs200897204	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267845	TTTTTTTTGAGACAG[A/G]GTCTTGGTCTGTCTC	57674
rs200898632	snp	C/T	0.00023116	0.0107483	missense	RNF213	GRCh38.p7	17:80332096	GACTGTCCACCTCCT[C/T]GAACTCGCAGAGGGC	57674
rs200944058	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324572	AAACTTTGAACCTAA[A/G]GGAAGAAAAATATTG	57674
rs200961756	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393870	CACTGCCCACCCCTC[C/T]TTTTTTTTTTCTTCT	57674
rs200962015	in-del	-/CTGGAGGTG			intron-variant	RNF213	GRCh38.p7	17:80314139	GTGATGGTGGAGGTA[-/CTGGAGGTG]ATGGTGGTGGTGTAG	57674
rs200964473	in-del	-/GAA			intron-variant	RNF213	GRCh38.p7	17:80315322	GGTGATGGTGGTGGT[-/GAA]GGTGATGGTGGAGGT	57674
rs200976081	in-del	-/ATATTTTG			intron-variant	RNF213	GRCh38.p7	17:80301056	ACCTTTGTCAGATGC[-/ATATTTTG]CAAAAATTTTCTCCC	57674
rs200985430	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313995	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs200989987	snp	A/G	9.90148e-05	0.00703545	missense	RNF213	GRCh38.p7	17:80345503	CAGGCCACCGACCCC[A/G]ACAAAACGTATGAGC	57674
rs200990051	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80303562	TTTCTTTTTTCTTTT[C/T]TTTTCTTTTTTTTTT	57674
rs201009778	snp	A/G/T	0.000120146	0.00774985	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351659	TTGTTTTTAAAATAG[A/G/T]TATTCTTTTTTTTTT	57674
rs201016173	snp	C/T	1.648e-05	0.0028705	synonymous-codon	RNF213	GRCh38.p7	17:80346291	TTTCAGGTGGTTCCA[C/T]GAGCACAGCGCGATG	57674
rs201022713	snp	A/G	0.00103087	0.0226797	intron-variant	RNF213	GRCh38.p7	17:80295507	GCTCTGGACACTGCC[A/G]GTGAATTCAAGTCCA	57674
rs201029318	snp	C/T	0.000133844	0.0081795	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363677	CCTGAAGCCCAGTCC[C/T]CAGGCGTGGCTACAG	57674
rs201050439	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80305453	AAAGTGCTGGGATTA[A/C]AGACGTGAGCCACTG	57674
rs201059019	snp	A/G	0.185155	0.241444	intron-variant	RNF213	GRCh38.p7	17:80318643	CAGTGGCGGGATCTC[A/G]GCTCACTGCAAACTC	57674
rs201062816	snp	C/T	3.29511e-05	0.00405887	intron-variant, missense	RNF213	GRCh38.p7	17:80319329	TGAACAATCTCTCCT[C/T]CTGGGAAACGGATTC	57674
rs201076138	snp	G/T	0.0766824	0.180169	intron-variant	RNF213	GRCh38.p7	17:80276088	ATTTATTTATTTATT[G/T]TTTGTTTTATTTATT	57674
rs201079508	snp	C/T	0.000579522	0.0170125	intron-variant	RNF213	GRCh38.p7	17:80273197	TTCCTTCCTAACACT[C/T]GCTTCTCTCTGAGAT	57674
rs201112053	in-del	-/GCTGAGGCAGGA			intron-variant	RNF213	GRCh38.p7	17:80304538	ACAGCTACTGGGGAG[-/GCTGAGGCAGGA]GAATGGCGTGAGCCT	57674
rs201118442	in-del	-/AC	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80294117	TTTTCTAATTATTTT[-/AC]AGTCAACCTCACTGG	57674
rs201124541	snp	A/G	0.0013058	0.0255185	intron-variant	RNF213	GRCh38.p7	17:80317152	CCGTGGCATTTAGTC[A/G]TGAGAGTGGGTGTGA	57674
rs201125428	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290426	GTGCGTGTGTGCGAG[A/C/T]GTGCGCGTGTGTGCA	57674
rs201141064	snp	C/T	0.000214995	0.0103659	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360102	TGGTGCAGAACCACA[C/T]GAACCTTTCCGAGAA	57674
rs201141090	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80279978	CGCACCGCGCTCCCC[C/G]CAGCCCCTGCCCATC	57674
rs201146285	snp	A/G	0.00199792	0.0315431	missense	RNF213	GRCh38.p7	17:80306280	CAGTTTATGAGAGAG[A/G]AGCAGCATTTGCTGA	57674
rs201148773	in-del	-/AAAA	0.078151	0.181571	intron-variant	RNF213	GRCh38.p7	17:80267218	GCGAGACTCTGTCTC[-/AAAA]AAAAAAAAGAAAAAA	57674
rs201150146	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395249	AGAGGCAAAAAAAAA[A/G]AAAATGAATTTTATT	57674
rs201156737	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80318074	CTTTCCGAAGTTAAA[C/T]CGTCTCTCCTTGGAA	57674
rs201159227	in-del	-/CCCG			intron-variant	RNF213	GRCh38.p7	17:80281078	CAGTCACACACACCC[-/CCCG]CCACACATACCCCAC	57674
rs201179733	snp	G/T	0.000568657	0.0168524	missense	RNF213	GRCh38.p7	17:80347308	CTTCAGTGGCAAGGA[G/T]GACATCCAAGCTTTG	57674
rs201218618	in-del	-/CACAAGCCAA			intron-variant	RNF213	GRCh38.p7	17:80278407	CATCTGTGCTCTGAG[-/CACAAGCCAA]GGCATTCGTGTGGAG	57674
rs201224867	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80281666	CCCCACTCACACACA[-/C]CCCAACATACGCAAG	57674
rs201231003	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355511	GCGGGGTGACCGGGA[A/T]TGGGGGCTTACAGGG	57674
rs201252098	in-del	-/GT	0.115788	0.21092	intron-variant	RNF213	GRCh38.p7	17:80290425	TGTGCGTGTGTGCGA[-/GT]GTGCGCGTGTGTGCA	57674
rs201281529	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80312943	GAGGAGAGGAGGGGG[C/T]GCAGCATCTCGCCGG	57674
rs201282643	snp	A/G	1.70188e-05	0.00291704	synonymous-codon	RNF213	GRCh38.p7	17:80289760	GAAGCCAGAGGGGAA[A/G]AACAGAAGTGCAGCT	57674
rs201289059	snp	C/T	8.01507e-05	0.00633	intron-variant	RNF213	GRCh38.p7	17:80289851	AGGTAGGGATGCCCC[C/T]GCAGGGGAGCAAAGG	57674
rs201294949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291876	TCCGGAGTGCAGGTG[C/T]CAATCCCGCGGTACT	57674
rs201295176	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80322576	GCGAGACTCTGTCTC[-/A]AAAAAAAAAATTTTT	57674
rs201312003	snp	G/T	0.00199792	0.0315431	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393478	GCTGCTGTGCTGAAA[G/T]GGAATCGAGAAATGA	57674
rs201358212	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313505	GTTGGTGGTGGTGGT[A/G]GTAGAGGTGATGGTG	57674
rs201361301	snp	A/G	5.01458e-05	0.00500704	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374589	TAAGACTGCTCTGAA[A/G]GTAGGATGGGCCCGT	57674
rs201373622	snp	C/T	0.000836986	0.02044	intron-variant	RNF213	GRCh38.p7	17:80317310	GCAGTCTTTTCAGGG[C/T]GTGAAGGCAAGCTGG	57674
rs201381326	snp	A/C	3.32906e-05	0.00407973	missense	RNF213	GRCh38.p7	17:80295560	TCCCACCATCAGGTG[A/C]AGAGATACCTGTGGC	57674
rs201402653	snp	G/T	0.00299557	0.0385851	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354536	TGGTTGGCAAGGGAA[G/T]CCTGCAACCAGGACG	57674
rs201418967	snp	C/T	0.000181191	0.00951644	missense	RNF213	GRCh38.p7	17:80295779	CCAGATGAGTTTCAC[C/T]GTGACCTAAGCCACA	57674
rs201421120	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291898	CGCGGTACTGGACGC[A/G/T]TCTCTCTGGAGAGCA	57674
rs201443069	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387970	TTTTTTTTTTTTTTT[C/T]TTTTTTTGAGACGGA	57674
rs201461095	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377437	AAAATATGCTCATGA[A/C]AAAAAAAAAAAAATC	57674
rs201462448	in-del	-/ATG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357847	AAAAATTAGCTGGGC[-/ATG]GTGGCACTGGGTGTG	57674
rs201470629	in-del	-/TGA			intron-variant	RNF213	GRCh38.p7	17:80314409	TGGAGGTGGTGGTGG[-/TGA]TGGTGGTGGTGGAGG	57674
rs201476526	snp	A/C	0.000362396	0.0134561	missense	RNF213	GRCh38.p7	17:80307188	TTGCGACTCCTGGAC[A/C]CTTACCGGGACAAGT	57674
rs201488528	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315501	GTGGTGGTGGTGGTG[A/G]TGGTGGAGGTACTGG	57674
rs201493500	snp	C/T	0.00580365	0.053555	missense	RNF213	GRCh38.p7	17:80328364	AGGATGAACAATGTG[C/T]TGTGGAGGAAGCACT	57674
rs201506620	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281350	CCCCCACACACACAC[A/C]CCACTCACACACACC	57674
rs201533911	in-del	-/TA	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80342560	CTCTCTCTCTATTTT[-/TA]TATATATATACACAC	57674
rs201535150	snp	A/G	0.000132553	0.00813997	missense	RNF213	GRCh38.p7	17:80346484	CCGAAACCGTATGAC[A/G]ACAGCAGGCTGCTTC	57674
rs201538272	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80284552	CCATCTCAAAAAAAG[-/A]AAAAAAAAAAAGCCT	57674
rs201545794	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394477	AAGAGTCCCCGAGCC[C/T]GGATCTTGTGCTGCT	57674
rs201547961	in-del	-/TTA			intron-variant	RNF213	GRCh38.p7	17:80315216	TGGAGGTGATGGTGG[-/TTA]TGGTGGTGGTGGAGG	57674
rs201549978	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349693	TCGCAGGTTTCTAGG[A/C]TCTGTCTAAACCTGG	57674
rs201559472	snp	C/T	0.000346618	0.0131601	missense	RNF213	GRCh38.p7	17:80347424	CTTCTCAGAAGGTGC[C/T]GGGTGGAGAGCAGGA	57674
rs201574428	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80274951	GTTGGGTGTGTGAGT[-/G]GGGGGTGTGTGTGTT	57674
rs201578981	in-del	-/A	0.0146672	0.084371	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360325	GAGTTTTTAGTTTTC[-/A]ACACTTTGTTTGTGC	57674
rs201579066	snp	C/T	0.000675169	0.0183611	synonymous-codon	RNF213	GRCh38.p7	17:80345065	TTTATTGGCGACACA[C/T]TGAGGGGCTTCAAGA	57674
rs201599942	snp	C/G/T	0.000148537	0.00861673	synonymous-codon	RNF213	GRCh38.p7	17:80298468	TGAGGACACCTGGGC[C/G/T]GCTCTGGAGGGACTC	57674
rs201620985	snp	C/T	0.00517971	0.0506263	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287905	TCTCCTGCCAGCCCC[C/T]GTCACCTGACTTTGC	57674
rs201634508	in-del	-/GGA			intron-variant	RNF213	GRCh38.p7	17:80315400	GATGGTGGTGGTGGT[-/GGA]GGTGGTACTGGAGGT	57674
rs201639829	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365436	CAGGTGCCCACGCTC[C/T]GTCTTGTCCCTTCAT	57674
rs201643716	snp	C/G	0.000347317	0.0131734	intron-variant	RNF213	GRCh38.p7	17:80313211	AGGGATGTGACTGAT[C/G]GTGATTCCTCATGGC	57674
rs201656916	snp	C/G	0.000131863	0.00811875	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375861	TGCAAGCCTCCACCC[C/G]ACGCCAGAGGTGAGT	57674
rs201658420	snp	A/G			missense	RNF213	GRCh38.p7	17:80289720	AAGTCGGTAAGAATG[A/G]ACAAGGGGAGCCTGA	57674
rs201660714	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80324573	AACTTTGAACCTAAA[-/G]GAAGAAAAATATTGT	57674
rs201683655	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356936	GGGTTTTTTTTTTTT[C/T]GAGACAGAGTCTCAC	57674
rs201705686	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359610	AGAGCGAGAGAAAGA[A/G]AGAAAGAAAGTAAAG	57674
rs201733659	snp	A/G	0.000181458	0.00952356	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393361	CTGAGAGACACTCTC[A/G]TAAGTTACATGCAAA	57674
rs201747319	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364398	TTCCTTGGTGGGAGC[C/T]GAGTGAGTGAGTGAG	57674
rs201756077	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260213	CGACGTCCACTGCAC[C/T]CGCCGGGCGCCCTCT	57674
rs201762188	snp	A/G	6.59794e-05	0.00574329	missense	RNF213	GRCh38.p7	17:80313100	CGAAAAGGTGGCTCC[A/G]AGAAGTTTTTACAAA	57674
rs201764802	snp	C/T	1.65597e-05	0.00287743	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319481	GGCGCTGAAATCTAG[C/T]TCTCTCCGGATTCCT	57674
rs201771673	in-del	-/AT			intron-variant	RNF213	GRCh38.p7	17:80281528	CCAACACACACATGC[-/AT]CCCACTCATACCACT	57674
rs201779262	snp	C/T	0.00115439	0.0239971	intron-variant, missense	RNF213	GRCh38.p7	17:80319422	GCTCCTCCGCTAACT[C/T]AGAGATTGGGAAGTG	57674
rs201798161	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80267824	AGCAGATTTTCTTTT[C/T]TTTTTTTTTTTTTGA	57674
rs201798357	snp	A/T	2.51259e-05	0.00354434	intron-variant	RNF213	GRCh38.p7	17:80289845	AAGGCAAGGTAGGGA[A/T]GCCCCCGCAGGGGAG	57674
rs201815403	snp	C/T	6.61048e-05	0.00574874	missense	RNF213	GRCh38.p7	17:80348051	TAGAGAGGCAGGGTC[C/T]CCGGGCCTTGACGGA	57674
rs201824278	in-del	-/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393870	CACTGCCCACCCCTC[-/T]TTTTTTTTTTCTTCT	57674
rs201832175	snp	A/G	0.00163963	0.0285854	intron-variant	RNF213	GRCh38.p7	17:80313007	TCCCTCTTGTGTGAC[A/G]ACAGGATTCTGCAGG	57674
rs201850343	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80297463	CAAAAAAAAAAAAAA[-/A]GTTGTTTTGGCCGGG	57674
rs201883585	snp	C/T	0.000115375	0.00759437	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354467	CGGGTATCCAAGATG[C/T]GCCTCAGTGTCTTTT	57674
rs201889709	snp	C/T	0.000138629	0.00832438	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288397	ATGGCCTGGGAGTGG[C/T]ACTGAGCCCTCGGCA	57674
rs201899752	in-del	-/AAAC	0.0217236	0.101931	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383506	GAGACATACATCTAT[-/AAAC]AAACAACACTGAAAT	57674
rs201902415	snp	C/T	0.00697544	0.0586435	intron-variant	RNF213	GRCh38.p7	17:80349941	CTGCTGCCCTCTCCC[C/T]CCCCAGCCGCAGCCG	57674
rs201905893	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355646	TTACAGGGGAAGAAG[C/T]GGGGTGGACGGGAAT	57674
rs201942414	in-del	-/GTA			intron-variant	RNF213	GRCh38.p7	17:80315963	GTGGTGGAGGTGGTG[-/GTA]GAGGTACTGGAGGTC	57674
rs201946707	in-del	-/G	0.0505692	0.150756	intron-variant	RNF213	GRCh38.p7	17:80261802	GCGGGTGGGTCACCT[-/G]GAGGTCGGGAGTTCG	57674
rs201957324	snp	A/G	8.25021e-05	0.00642217	missense	RNF213	GRCh38.p7	17:80306434	CAGGGATTTACTACC[A/G]GCTTCCGGGACTTGA	57674
rs201966433	snp	A/G/T	0.148415	0.23765	intron-variant	RNF213	GRCh38.p7	17:80276092	ATTTATTTATTTTTT[A/G/T]TTTTATTTATTTATT	57674
rs201968632	snp	C/G	3.29739e-05	0.00406028	intron-variant	RNF213	GRCh38.p7	17:80307233	ATGCAGTCTCTCCCT[C/G]ACATGCGGCCCCCGG	57674
rs201969235	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80304658	AAATAAATAAATAAA[-/T]TAATAATAATAATAA	57674
rs201991792	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80294945	TTGTCCTGCAACAGC[C/T]TATGATTTATGAAGG	57674
rs202004102	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314022	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs202006755	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364710	ATCACTAGGCCATTA[C/T]ATTTTCCATGTTTAA	57674
rs202011763	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378331	CTGTGCGCCATGGGG[A/G]AAGAACTGTTGATTA	57674
rs202020035	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80315978	GGAGGTACTGGAGGT[C/G]ATGGTGGTGGTGGAG	57674
rs202024727	in-del	-/A	0.0178098	0.0926698	intron-variant	RNF213	GRCh38.p7	17:80308950	AAGGAGCTAGTCATC[-/A]AATGGTAACCATTTT	57674
rs202049391	in-del	-/AAG	0.105214	0.203807	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375552	TAAAAGAAAAAAAAA[-/AAG]AATTAGCCGGACATG	57674
rs202078935	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80284379	CAAAAAAAACAAAAA[A/C]AAAAACAAAACAAAA	57674
rs202087583	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317308	GGGCAGTCTTTTCAG[A/G]GCGTGAAGGCAAGCT	57674
rs202087716	snp	A/C	8.31497e-05	0.00644732	synonymous-codon	RNF213	GRCh38.p7	17:80273263	GAACAATAACTCCAC[A/C]ATGGCGTCGGCCTCG	57674
rs202096577	snp	C/T	0.00117101	0.0241688	missense	RNF213	GRCh38.p7	17:80346419	GGGTGTGTTACCATG[C/T]CTCTTTAGAAAAGAA	57674
rs202116232	snp	C/T	0.0002854	0.0119423	missense	RNF213	GRCh38.p7	17:80347021	CCTGCCAAGATGAAC[C/T]GGGGCATTTTTGTGT	57674
rs202117335	in-del	-/C	0.0205511	0.0992634	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320066	CATCTGTCAAAAGTT[-/C]CAGTTCAGCAGGTTT	57674
rs202119991	snp	A/G/T	0.000232781	0.0107864	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354116	GCACGCGCAATATGC[A/G/T]GAGGGTGGTGCTCCT	57674
rs202124314	snp	A/G	0.00199792	0.0315431	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353698	GGGACCTCCCCTTGT[A/G]CTGCTGGTGATGCTT	57674
rs202133062	snp	G/T	1.67728e-05	0.00289588	intron-variant	RNF213	GRCh38.p7	17:80295531	AAGTCCATGGTTCAT[G/T]CATCTTCCTCTTCTC	57674
rs202142237	snp	A/G	0.00161231	0.0283471	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363740	CATCTGCTCCGATGA[A/G]CACATGCAAGGCAGC	57674
rs202143169	snp	A/G	0.000527131	0.0162261	missense	RNF213	GRCh38.p7	17:80345918	CCTGCAATCCATACC[A/G]GAAGCACTCTGAGGA	57674
rs202164487	snp	A/G	0.000133089	0.00815641	synonymous-codon	RNF213	GRCh38.p7	17:80273278	AATGGCGTCGGCCTC[A/G]GAGGGTGAAATGGAG	57674
rs202176135	snp	C/T	6.68192e-05	0.00577972	intron-variant	RNF213	GRCh38.p7	17:80298525	GCTAGATACGTAAGT[C/T]GTAGAGTTGTGCTTA	57674
rs202178409	snp	C/T	1.65318e-05	0.002875	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363282	AGCCTGATGGAAGCC[C/T]GTTGGAACCATGAGC	57674
rs202189357	in-del	-/TGA			intron-variant	RNF213	GRCh38.p7	17:80314295	TACTGGAGGTGATGG[-/TGA]TGGTGGACGTGATGG	57674
rs202211290	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366668	AAGGATGGCTCAAAA[A/T]AAAAAAAAAAAAATC	57674
rs202223629	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80276897	CTCTACTAAAAATAC[-/A]AAAAAAAAAATTAGC	57674
rs202230519	snp	A/G	1.65718e-05	0.00287848	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381020	CAAACAATGGGCTCA[A/G]TTAAGAACCTGCTTT	57674
rs202246179	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80284214	ACAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGAT	57674
rs267605083	snp	C/G/T	1.65091e-05	0.00287303	RNF213	17	allele_origin=G(somatic)/C(germline)	17:80348148	CGTGGTCCGGCTGAG[C/G/T]GCCTACTCGCTGGGC	57674
rs367544330	snp	C/T	0.0023933	0.0345097	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352523	CAGCTATTTATGACA[C/T]AGAAAAGTTGGTATT	57674
rs367546284	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326066	CGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC	57674
rs367555890	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80301888	ATCATCCTGAGTGTC[C/T]ACCCGCAGATGAGTG	57674
rs367559865	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314587	TGGTGGTGGTGGTGG[A/T]GGTAATGGAGGTGAT	57674
rs367583479	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80280090	GGCAGGCATGCTCTT[A/T]CCTCTGTGGGCTGGG	57674
rs367584488	snp	C/G	1.64789e-05	0.0028704	synonymous-codon	RNF213	GRCh38.p7	17:80346069	GAGCCTGATTCCTCT[C/G]GTGTGGGACTTTGGA	57674
rs367587324	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80292075	TCACTTGCAGGAGGA[A/G]ACATGCAAAGGACTT	57674
rs367615455	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80315795	GGTGGTGGTGGTGGT[G/T]GTGGTGGAGGTGGTG	57674
rs367617075	snp	C/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304604	GAGATCACACCACTG[C/G]ACTCCAGCCAAGGCA	57674
rs367622664	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80280097	ATGCTCTTTCCTCTG[A/T]GGGCTGGGGCTTGGC	57674
rs367650147	in-del	-/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351674	TTAAAATAGGTATTC[-/T]TTTTTTTTTTCTTTA	57674
rs367665359	in-del	-/TTTA/TTTATTTA	0.41083	0.260318	intron-variant	RNF213	GRCh38.p7	17:80299534	TATTACCAGAGAAAG[-/TTTA/TTTATTTA]TTTATTTATTTATTT	57674
rs367666183	snp	C/T	3.50933e-05	0.00418872	intron-variant	RNF213	GRCh38.p7	17:80306489	TGTCTGAAGTCGGCT[C/T]TGGAGTCCTGGCTTA	57674
rs367667069	snp	A/G/T	6.60103e-05	0.00574468	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354406	CAACAGCTCAGCCAC[A/G/T]GCCATGCTGAACGTC	57674
rs367681353	snp	A/G	0.000148262	0.00860865	missense	RNF213	GRCh38.p7	17:80345645	TCCTTAGCGACCTGC[A/G]GCGTGGTGGTACCAA	57674
rs367700707	snp	A/G	1.65127e-05	0.00287334	missense	RNF213	GRCh38.p7	17:80347391	CCATGCAGCTGATCA[A/G]ACAGAACATCTTTGG	57674
rs367704039	snp	A/C			stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386275	CCTACCCAAAGACTA[A/C]TGCAGCACTGACTTG	57674
rs367752941	snp	C/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369915	GCCCTGGCTTTTTCT[C/G]TTCATCGCAGCGTTT	57674
rs367753246	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80329368	CCTTCTGAAGTTTCA[A/G]TGTGCTGCGCCATCA	57674
rs367758434	snp	C/T	0.000154008	0.00877384	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288152	AATTCCAGGACCACA[C/T]GGAAGGGGAGGACCA	57674
rs367758826	in-del	-/ATA			intron-variant	RNF213	GRCh38.p7	17:80265370	CCACTTCTATTAATA[-/ATA]GTGCGGAGAGCACTG	57674
rs367766924	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315403	TGGTGGTGGTGGTGG[A/T]GGTACTGGAGGTGAT	57674
rs367771592	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319818	CGCAGGCAATGCCAC[A/G]TGAGGAAGCTCCCTG	57674
rs367776362	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355497	TCACAGAGGAAGAAG[C/T]GGGGTGACCGGGAAT	57674
rs367779663	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80305981	CTGCATATTTTTGTT[C/T]TCCACATAGCCTTTA	57674
rs367780163	snp	A/G	3.31367e-05	0.00407029	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358483	GAATAATGAAAGGTG[A/G]GTGGAAGGCTTTCTT	57674
rs367788260	snp	A/G	5.64685e-05	0.00531329	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386913	CTGACTCCTGCCACT[A/G]CTGCTCATTTGGTGT	57674
rs367798371	in-del	-/CAGGCTGGTCTCGATCTCCTGACCTCAAGTGATCTGCCCGTCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGCGCCCGGCCTGTCCTCTCTCTTCTTGTGCTTTCACATACTTGTTTTATTCACCAGTTTATGTTTAGGTGTAAAGTAAGGATTTAACTTGATGTTTTCCTGAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391976	TTTCACCATGTTGAC[lengthTooLong]TAGATCATCAAACTC	57674
rs367799805	snp	C/T	1.65479e-05	0.0028764	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386295	GCACTGACTTGGATC[C/T]GGACACTGAGTTTGA	57674
rs367803668	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80337373	AGGAAACGTGGAACA[A/G]CGAGTACAAAGCAGC	57674
rs367812816	snp	A/G	0.000116178	0.00762072	intron-variant	RNF213	GRCh38.p7	17:80348329	ATCCCCTGTCACCCA[A/G]GAGTCCTAAATCCCT	57674
rs367813903	snp	A/G	6.75995e-05	0.00581336	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373126	CAAGCCCGGCCGCCC[A/G]CACCAGTGGGTGTTT	57674
rs367820011	snp	A/G	8.30696e-05	0.00644421	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390171	CCCCAAACCCAAACC[A/G]AGGAGCGCTTCCGCC	57674
rs367824518	snp	G/T	1.65345e-05	0.00287524	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380987	GTCCCAGAGTTCCCA[G/T]GTATAACCCAGTGCT	57674
rs367840099	snp	C/T	1.67438e-05	0.00289338	synonymous-codon	RNF213	GRCh38.p7	17:80346678	TCTCGCCAAGACCAT[C/T]GTGGCAGACGCCATG	57674
rs367877144	snp	C/G	1.64751e-05	0.00287007	intron-variant	RNF213	GRCh38.p7	17:80291616	AGCCAACCGTATCCT[C/G]TTCATTCACAGAGAC	57674
rs367879018	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80319235	TGCAATAGTTGCTGG[A/G]ACACCAAAGGCTTAG	57674
rs367885315	snp	C/T	3.29701e-05	0.00406005	synonymous-codon	RNF213	GRCh38.p7	17:80347593	CCAGCTCTGCAGAAA[C/T]ATCAATCGTGTGAAG	57674
rs367892183	snp	C/T	1.65732e-05	0.00287859	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369822	ATGTTGTGGATAAGA[C/T]TCCTGTCATCCGCTC	57674
rs367895356	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80267946	TGCCTCAGCCTCCCA[A/C]GTAGCTGGGATTACA	57674
rs367919238	in-del	-/TT	0	0	intron-variant	RNF213	GRCh38.p7	17:80307875	TTTTTTTTTTTTTTT[-/TT]AAAGGGAAATAATAG	57674
rs367919620	snp	C/G/T	3.29549e-05	0.00405911	missense	RNF213	GRCh38.p7	17:80345917	GCCTGCAATCCATAC[C/G/T]GGAAGCACTCTGAGG	57674
rs367938983	snp	C/T	0.000938699	0.0216441	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363329	GGTATGGCCCTCCTC[C/T]GCCTGCCCTGAGCAA	57674
rs367968390	snp	C/T	0.000164745	0.00907442	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383728	ATCAGCCAAGATAAG[C/T]GTATCAGCTCTAACC	57674
rs367985993	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294437	ACATAGTTAGAGATC[C/T]GTTGCAAGTCTCAGG	57674
rs367995834	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367076	CCAGCAGACAGGTAA[C/T]TGGTGTCTTTATCAG	57674
rs368005329	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80264200	TCTTCCCCTTGGGAA[A/T]GAGAAGTGTCGGGCT	57674
rs368031743	snp	C/T	0.000153988	0.00877328	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386327	ATCCTCTTGCCACGC[C/T]GACGGGGCCTGGGCC	57674
rs368044060	snp	A/G	0.000378816	0.0137573	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389944	CTCTTCCTCTCTGCT[A/G]GACAGAGGGACTGCG	57674
rs368047631	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387683	ACCTGCCTGGCCTCT[C/T]ATGGCATATGGGATA	57674
rs368054349	snp	C/G/T	3.30651e-05	0.00406591	stop-gained, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360082	AGGTGAGATGGCCTA[C/G/T]ATCGTGGTGCAGAAC	57674
rs368062489	snp	C/T	1.6477e-05	0.00287024	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374426	AAGACATTCCTCCCA[C/T]TGTTCACCCCCAACT	57674
rs368073561	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371238	AACTAACCTCTAGAC[A/G]TGACCATTTATCACT	57674
rs368079725	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80269256	ACACCCTCACAGACA[-/CA]ACCAGAACAATACTT	57674
rs368081593	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392900	TGGCCTAGGATTTTA[A/C]GTCTTAACGAGCATT	57674
rs368089058	snp	C/T	0.000114162	0.00755433	missense	RNF213	GRCh38.p7	17:80334201	GACATCAGCGAGGCC[C/T]GGTGCAAGGGGCTGC	57674
rs368092028	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326295	ATACCCAGCCTGTTT[A/G/T]TAAGTTGGATAGAAT	57674
rs368110355	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381439	TTCATCTTAGAAACC[A/G]CCTTCCGACTCTATG	57674
rs368142747	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328939	ACTCTCTGTTTTCCA[C/T]AGAATTACATTTCCT	57674
rs368143475	in-del	-/CC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393268	TACACACGTGAGCCA[-/CC]CACAGTGCTGGGCTT	57674
rs368173829	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296742	AGTCTGGAGTGCAGT[A/G]GAGCAATCAGCTCAC	57674
rs368173859	snp	C/T	0.000114371	0.00756123	intron-variant	RNF213	GRCh38.p7	17:80328002	TGAGTAAGCATCGAG[C/T]CGATACGCACTTCAG	57674
rs368183911	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80284136	AGGCCGAGGCGGGTG[G/T]ATCACCTGAGGTCAG	57674
rs368189896	snp	A/C	0.426047	0.177503	intron-variant	RNF213	GRCh38.p7	17:80315165	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs368197780	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80294118	TTTCTAATTATTTTA[-/CA]GTCAACCTCACTGGG	57674
rs368199663	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281565	CCCCCCAAGACAAAC[A/G]CCCCACTCACACCAC	57674
rs368214116	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269571	TTCTATCTGTCCATC[C/T]ATCTATACTATCTAT	57674
rs368221664	in-del	-/GAG	0.0034538	0.0414122	cds-indel	RNF213	GRCh38.p7	17:80290665	ATAAAGTCTTCATCA[-/GAG]GAGGAGAAGAATTTG	57674
rs368229784	snp	C/G	0.000153988	0.00877328	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372712	AGCTGCAGATTTCCT[C/G]TCGGAGCCTGAGGGA	57674
rs368247498	in-del	-/TGGAGGTAA			intron-variant	RNF213	GRCh38.p7	17:80315046	TGGTGAAGGTGATGG[-/TGGAGGTAA]TGGAGGTGATGGTGG	57674
rs368263103	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80304584	GGCAGAGCTTGCAGT[A/G]AGCCGAGATCACACC	57674
rs368266183	snp	A/G	0.000229305	0.0107051	synonymous-codon	RNF213	GRCh38.p7	17:80339482	CCTGAACTTCTACAC[A/G]GCAGAGCAGCTGGTT	57674
rs368280645	in-del	A/TT	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366680	GATGACATTTACAGA[A/TT]TTTTTTTTTTTATTT	57674
rs368281638	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277427	ACATGGGGAAACCCC[A/G]TCTCTACTAAAAATA	57674
rs368315497	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357075	AGGTGCCTGCCACCA[C/T]GACTGTAATTTTTGT	57674
rs368316429	snp	A/G	0.000149037	0.00863114	synonymous-codon	RNF213	GRCh38.p7	17:80346882	TGAGGTGGGGCTGGC[A/G]GAAGACTCACCCAAA	57674
rs368324738	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376174	CTGAAAAATTTCCCC[C/T]TCAAATGGTGGTGAT	57674
rs368336655	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314546	GGTGAAGGTGATGGT[A/G]GAGGTAATGGAGGTG	57674
rs368339925	snp	C/T	0.000830445	0.0203601	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367697	GTCGCCCGGCCTGGC[C/T]GCCCTCAGCCCTCCC	57674
rs368345205	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390424	CTTGCCCTGTTACCC[A/G]GGCTGGAGTGCAGTG	57674
rs368356229	snp	C/T	1.64836e-05	0.0028708	synonymous-codon	RNF213	GRCh38.p7	17:80345544	CAATATGCTTAAAAT[C/T]CTTGCCATCGAGATG	57674
rs368359130	snp	A/G	8.23621e-05	0.00641672	intron-variant	RNF213	GRCh38.p7	17:80343843	GTTTACACCTCGTGC[A/G]ATTCTGTTCTTAGGT	57674
rs368365560	snp	C/T	1.66291e-05	0.00288345	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354115	TGCACGCGCAATATG[C/T]GGAGGGTGGTGCTCC	57674
rs368370792	snp	A/C	3.29522e-05	0.00405894	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369593	TTCAAGGACAACGCT[A/C]CGCCTGAGAAGGAAG	57674
rs368415931	snp	A/G	0.000115326	0.00759274	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358364	TTCATCGACAGAGAC[A/G]GCAACCTAGAGTTAC	57674
rs368419803	snp	C/T	1.65806e-05	0.00287924	missense	RNF213	GRCh38.p7	17:80295648	CTGTGGACTGCCCAG[C/T]GAGGAGTAAACTGAA	57674
rs368421294	snp	C/T	0.000117922	0.00767769	missense	RNF213	GRCh38.p7	17:80350305	TTTTCTTTCAGAAAC[C/T]GTTTAACGAATACAG	57674
rs368432473	snp	A/G	0.000234659	0.0108293	intron-variant	RNF213	GRCh38.p7	17:80336411	TCTAATGCAGATTTT[A/G]TTGAATAGAGCATTG	57674
rs368439662	snp	A/G	3.30077e-05	0.00406236	synonymous-codon	RNF213	GRCh38.p7	17:80347881	CACGGTGCTGGAGAA[A/G]TGGCAGAAGAGCATC	57674
rs368442720	snp	A/C	1.67343e-05	0.00289255	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386214	TGTGAGGAGTTGGAA[A/C]TCCTCTCTGCTTAAG	57674
rs368452080	snp	C/G/T	9.88381e-05	0.00702929	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376294	TGTTAAGTTTTTTTC[C/G/T]TGTCAGCAATGTGAA	57674
rs368452961	snp	C/T	6.67512e-05	0.00577678	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373049	GAGAACGACTGGCAC[C/T]GGGTGTACCTGGTGC	57674
rs368452969	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80344023	CAGCGCTGGTCTGTA[C/T]TGTGGGGCGTTTTCG	57674
rs368455596	snp	C/T	6.60546e-05	0.00574656	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352895	GGGCTGAGCAGCAGC[C/T]GGGAAAGACACAAAG	57674
rs368461436	snp	C/T	0.000117124	0.0076517	intron-variant	RNF213	GRCh38.p7	17:80295541	TTCATGCATCTTCCT[C/T]TTCTCCCACCATCAG	57674
rs368462132	snp	A/G	0.000164718	0.00907368	synonymous-codon	RNF213	GRCh38.p7	17:80291658	CCGCGTTCTTGTTGA[A/G]GGCATTGTCTGCATT	57674
rs368498587	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80303557	TTCCTTTTCTTTTTT[C/T]TTTTCTTTTCTTTTT	57674
rs368514350	snp	A/G	1.65682e-05	0.00287817	missense	RNF213	GRCh38.p7	17:80313012	CTTGTGTGACAACAG[A/G]ATTCTGCAGGACAGA	57674
rs368541533	snp	G/T	0.000696883	0.0186536	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383117	CCTCGGTCCAGAAAG[G/T]AAGGGTCCCGGCGTC	57674
rs368578211	snp	C/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380868	ACCGGCCACGTGCTG[C/G]GCAACCCGCAGCGGA	57674
rs368599231	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315036	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs368634922	snp	A/G	5.62825e-05	0.00530454	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372772	TCCTTTGGGTTTAAA[A/G]ACTCCGTTATTTAGA	57674
rs368642459	snp	A/C	6.63592e-05	0.00575979	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383020	TCAACTAAAGAAATG[A/C]GGAACAACTGGGAAA	57674
rs368645346	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80309743	TCTCCCATGGATCAG[-/T]TTTTTTTTTTGTTTT	57674
rs368646799	snp	A/G	3.29603e-05	0.00405944	intron-variant, missense	RNF213	GRCh38.p7	17:80319385	ACCCAGCTAAGGGCT[A/G]TGAAGCACCCGCTGG	57674
rs368651945	snp	A/G/T	0.00011458	0.00756816	synonymous-codon	RNF213	GRCh38.p7	17:80339662	CATGGAAGAGCTCCC[A/G/T]CTGATGCTCTTATCA	57674
rs368654526	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314509	TGGTGGTGGTGGTGG[A/T]GGTAATGGAGGTGAT	57674
rs368662867	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287096	CCAGGCACGGTGGCT[C/T]ACGCGTGTAATCCCA	57674
rs368664404	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80294255	GCCAGCTGGGCAGCC[G/T]GCACCTTCCTCCAGG	57674
rs368671606	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80311488	TTTTCTGTCGGCCCC[C/T]GCCCCCTGCGTGCTG	57674
rs368717198	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387234	CATCAGCTTCCCAAA[C/T]AGCTGAGATCACAAG	57674
rs368720211	snp	A/C	3.3712e-05	0.00410547	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287790	AAATCTAAGAAATAA[A/C]GTGAGTGTCTCTCTT	57674
rs368736557	in-del	-/CTCACTGCAACCTTGG	0.0201227	0.0982671	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390452	GTGGAGTAATCTCAA[-/CTCACTGCAACCTTGG]CTCACTGCAACCTCT	57674
rs368742341	snp	A/G	0.000115305	0.00759205	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390005	ATTTGCTCTTCCGTC[A/G]TTTTAGGAGCCATTT	57674
rs368742645	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365567	TCCCGGACACGCACA[C/T]GCCACACCAGCTCGT	57674
rs368744366	in-del	-/CAAA			intron-variant	RNF213	GRCh38.p7	17:80311207	AAGCAAACAAACAAA[-/CAAA]AAACCTTTGCAATAC	57674
rs368747123	snp	C/T	3.30426e-05	0.0040645	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367748	CCTGCCTTTCTTCAG[C/T]GTCTTCGAGAGAACT	57674
rs368763393	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80333570	GTGGTGTCAGGTGCC[C/T]GTAATCTCAGCTACT	57674
rs368768197	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366308	CTGTTTAACTTTATG[C/T]AGAGGCACTGTATTG	57674
rs368777091	snp	A/G	0.00157916	0.0280551	intron-variant	RNF213	GRCh38.p7	17:80291835	CTCAGGAGGTAAGTC[A/G]TGGCAGCAGGCTGTC	57674
rs368777469	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374716	CACGTGACACTGTAT[C/T]GGAAGTCACGTGCCC	57674
rs368811368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317405	GGTGAATCACAGCTC[C/T]GTGTTTCTGTTTCTG	57674
rs368829453	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270630	GGCATCTCTTTGGAA[A/G]TTAAGAGACCACATG	57674
rs368830359	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80350714	TGAGGTGGGAGGATC[A/G]CTTGAGCCTGGGAGG	57674
rs368837975	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80264578	GAGGGCACCTCATTC[C/T]TCCAGCTGCTTCTAT	57674
rs368850066	snp	C/T	0.000344175	0.0131137	missense	RNF213	GRCh38.p7	17:80337649	CATGGGTCTGTGGAA[C/T]GCTCATCCCTGACCC	57674
rs368875063	in-del	-/G	0.00303339	0.0388265	intron-variant	RNF213	GRCh38.p7	17:80344052	GCCTGGCGTGGGGGG[-/G]CTCTTGGGTTCTTTC	57674
rs368929895	snp	C/G/T	0.000131902	0.00811996	missense, synonymous-codon	RNF213	GRCh38.p7	17:80289682	GACCAAGACCAAGGA[C/G/T]GAGATGGCTGCTGCT	57674
rs368932791	snp	A/C	1.65078e-05	0.00287291	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352925	GACAGTTGTGGGTGG[A/C]TTCACTCTTCACAGG	57674
rs368932915	snp	C/T	0.000184171	0.00959436	intron-variant	RNF213	GRCh38.p7	17:80317176	GGTGTGACCTGTGTG[C/T]GGGTTTTGCAGGTCT	57674
rs368942647	snp	C/T	6.58903e-05	0.00573941	synonymous-codon	RNF213	GRCh38.p7	17:80345265	CGTTTTCTTCAATGA[C/T]GACCACACAACCATG	57674
rs368985577	snp	C/T	4.94401e-05	0.00497168	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367780	TGACGTGAAGACGCA[C/T]GGGCCTTTTGAGGCC	57674
rs368987237	in-del	-/GTT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381138	GTTATACATCTTCAT[-/GTT]TCCCCCTGTGGCGTA	57674
rs368992364	snp	A/G	0.00016798	0.00916306	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376568	GGCCACAATTCCATC[A/G]GCCTTCACTGGAACA	57674
rs369020182	snp	C/T	2.04643e-05	0.00319871	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351850	TTATGTATTTATTTA[C/T]TTATTTGTATCTATT	57674
rs369041141	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80339882	GTCTGTGGCCACTCC[A/G]AGGTGTTGCCAGCCG	57674
rs369046882	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314035	TGATGGTGGTGGTGG[A/T]GGTGATGGTGGAGGT	57674
rs369054224	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80285184	CGTGTGCTTTGTCCC[A/C]TTTGGTCACCCTCAG	57674
rs369066805	snp	A/G	0.000199947	0.00999667	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319524	CAGTCCCTGCTGCTC[A/G]CACCATCCTGCATGT	57674
rs369079303	snp	A/G	0.000148752	0.00862286	missense	RNF213	GRCh38.p7	17:80348054	AGAGGCAGGGTCCCC[A/G]GGCCTTGACGGAGGA	57674
rs369088075	snp	A/G	3.429e-05	0.00414051	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363757	ACATGCAAGGCAGCG[A/G]GAGCCTGGCCCAGGC	57674
rs369097124	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374746	CACACTAGCCAGGTG[C/T]GCCCTGGAGGCTGTG	57674
rs369121819	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389169	CCTGCTTTTCATTTC[C/T]CAGGACTCCCTCCCC	57674
rs369126465	snp	A/C/T	8.37747e-05	0.0064716	stop-gained, synonymous-codon	RNF213	GRCh38.p7	17:80347152	CTTTGCCAAAGCCTA[A/C/T]GAAACGGTGTGTAAG	57674
rs369127560	in-del	-/GAGAAAGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359610	AGAGCGAGAGAAAGA[-/GAGAAAGA]AAGTAAAGAAAGAAA	57674
rs369136434	snp	A/C	6.59435e-05	0.00574172	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374519	ACGGCGATGAATACA[A/C]GGCTCTCCGTGATGC	57674
rs369199800	snp	A/C	1.64844e-05	0.00287087	intron-variant	RNF213	GRCh38.p7	17:80307230	ACGATGCAGTCTCTC[A/C]CTCACATGCGGCCCC	57674
rs369201841	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384549	AACTTCTGTTGGTCA[C/G]TTGAGGAGTATGAGT	57674
rs369215015	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361801	TCTTGCCCAGCTCCA[C/T]GGAGAGCCGCAGCAG	57674
rs369254333	snp	C/T	0.000238152	0.0109096	synonymous-codon	RNF213	GRCh38.p7	17:80339815	GATGGGTGGGTCTCC[C/T]GTGGAGCGTTGTCTC	57674
rs369296898	snp	C/T	1.65091e-05	0.00287303	utr-variant-5-prime, intron-variant	RNF213	GRCh38.p7	17:80263638	AGGCTGCCAGCGACT[C/T]CTGCTCTTGCTTCTG	57674
rs369303636	snp	A/C	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386643	ACATAGAGCCCTAGG[A/C]CCGCATGCCTGGCCT	57674
rs369315397	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80344741	ACCTGCAGGCCTCCC[A/G]AAGAGGTGATAGACA	57674
rs369335570	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80313974	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs369347059	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320686	TGAGCCACCGCGCCC[A/G]GCCGAGCATAATGTT	57674
rs369348436	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297307	ATACAAAATTTAGCC[A/G]GGCGTGGTGGTGCAT	57674
rs369375903	snp	A/G	3.3678e-05	0.0041034	intron-variant	RNF213	GRCh38.p7	17:80291864	TCTGCTCACCCCTCC[A/G]GAGTGCAGGTGCCAA	57674
rs369380805	snp	A/G	9.90606e-05	0.00703708	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375881	CAGAGGTGAGTAACC[A/G]CCTGCAGGGCTGTGT	57674
rs369386142	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80285960	GGATTACAGGCCTGA[C/G]CCACCGCACCTGACC	57674
rs369430847	in-del	-/GC	0.029116	0.117091	intron-variant	RNF213	GRCh38.p7	17:80290481	TGTGCACGTGTGTGT[-/GC]GCACGTGTGTGTGTG	57674
rs369443728	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307408	TTACTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGA	57674
rs369469004	in-del	-/GTTTGTTT	0	0	intron-variant	RNF213	GRCh38.p7	17:80265045	TCCATGTTTGTTTTT[-/GTTTGTTT]TTTTTTTTTTTTTTT	57674
rs369469126	snp	A/G	7.68034e-05	0.00619644	intron-variant	RNF213	GRCh38.p7	17:80298291	TCCCTGGCCAGCTCA[A/G]CTCACTGCGGGATCT	57674
rs369472436	snp	A/C/G	8.68906e-05	0.00659083	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288048	TGACGGCCTCTCCGC[A/C/G]CCCACCGAGGTTGGC	57674
rs369477713	snp	C/T	1.65987e-05	0.00288082	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381028	GGGCTCAGTTAAGAA[C/T]CTGCTTTCGCTTCTT	57674
rs369484242	snp	C/T	6.62658e-05	0.00575574	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353059	GGAGACTTGCCTGAG[C/T]GTGAGTCACGAGGCG	57674
rs369507354	in-del	-/TTCTTTTCTTTT			intron-variant	RNF213	GRCh38.p7	17:80303555	TATTCCTTTTCTTTT[-/TTCTTTTCTTTT]CTTTTTTTTTTTTTT	57674
rs369523345	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361402	GTGCATGCCTGTAGT[C/T]CCAGCTACTTGGTAG	57674
rs369525047	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299431	TTATACCTTTGCATA[A/G]TGCTGGCTTAAAGGA	57674
rs369531347	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314173	TGTAGGTGATGGTGG[A/T]GGTGATGGTGGTGGT	57674
rs369546167	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395309	GAGTTTTGCTGCTAA[A/G]GAACTCTTCTCTCTG	57674
rs369547876	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330519	CTTGGCATCCCGTGC[A/G]TGGTCCTCCCATGGC	57674
rs369553481	snp	C/T	1.64819e-05	0.00287066	missense	RNF213	GRCh38.p7	17:80346302	TCCACGAGCACAGCG[C/T]GATGCTCTTAGCGCA	57674
rs369576337	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355758	TCACGGAGGAAGAAG[C/T]GGGGTGAATGGGAAT	57674
rs369578924	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314829	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs369583881	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80281136	TCACACACACCCCCA[C/T]ACCCCACTCACACCA	57674
rs369601590	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80306023	AAAGTAGAGACAGGG[C/T]CTCACTAGGTTCCCC	57674
rs369621531	snp	A/G	0.000278125	0.0117892	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381772	ATCACACAGCACAAC[A/G]GCAGCGCAAGCAGGC	57674
rs369621569	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315529	TGGAGGTGATGGTGG[A/T]GGTACTGGAGGTGAT	57674
rs369626421	snp	A/G	3.29592e-05	0.00405938	synonymous-codon	RNF213	GRCh38.p7	17:80346054	CCATGCTCTGCCCCC[A/G]AGCCTGATTCCTCTG	57674
rs369647453	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288438	GCTGCAAGGTGCTGG[C/T]GTTGCTTCCCTGCCG	57674
rs369649993	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383856	AAGAATTACAGTTGA[A/G]TACCTCCAGCACATT	57674
rs369667044	snp	A/G	0.000437904	0.0147905	synonymous-codon	RNF213	GRCh38.p7	17:80337940	GCTTTTGAACAAGTT[A/G]ATGCTGATGTCTGGC	57674
rs369670065	snp	A/G	8.26071e-05	0.00642625	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354565	CGCTCTCCAGGAGGC[A/G]GGCACATTCAGGTAC	57674
rs369674946	snp	A/T	1.66963e-05	0.00288927	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369917	CCTGGCTTTTTCTCT[A/T]CATCGCAGCGTTTTG	57674
rs369680818	in-del	-/ATGGTG			intron-variant	RNF213	GRCh38.p7	17:80313718	GTGGTGATGGAGGTG[-/ATGGTG]GTGGTGGTGGAGGTG	57674
rs369701750	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390499	CCTCCCAGGTTCAAG[C/T]GAGTCTCATGCCTCA	57674
rs369732955	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80298363	CCAAAGATGCATGGA[C/T]ACAAGGACGTACACC	57674
rs369734517	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80294802	CATCACAGACGGGCC[A/G]AGGAAGGACCTGGTG	57674
rs369737066	snp	C/T	1.64741e-05	0.00286998	stop-gained	RNF213	GRCh38.p7	17:80344930	CCGGAGGAATGCCTC[C/T]AGCATTTCCTGTTTC	57674
rs369739492	snp	C/G/T	1.6477e-05	0.00287024	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374445	TCACCCCCAACTAAC[C/G/T]TCTGTATTCCAGGGG	57674
rs369740181	in-del	-/TCTT			intron-variant	RNF213	GRCh38.p7	17:80269700	CTATCTATGTATCTA[-/TCTT]ATGTATCTATCCATT	57674
rs369740836	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377742	CTCATTAGCCAATGT[A/G]TGTCCTGTTCTCTTC	57674
rs369768166	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80262465	CAGATAATCACTCAG[A/G]TGATCTCAGAGCTGC	57674
rs369783438	snp	C/G	0.000149479	0.00864401	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386440	CAACAGGTTTGTGCA[C/G]GAGCCACCAGGAAGT	57674
rs369786853	snp	C/T	3.69788e-05	0.00429977	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353551	ACGGCCATGAGGAGG[C/T]GATGGAGACGGAGGC	57674
rs369790005	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80322161	CCCCCCCACCCCCCC[C/T]TTTTTTTTTTTTTTT	57674
rs369793176	snp	C/T	4.94205e-05	0.0049707	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368006	GGGAGATGCAAAGGA[C/T]CCCGTCTGTCTGCCC	57674
rs369805271	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355047	ACCCATGAGACTAAC[A/C]TTGATTATCTTGGAT	57674
rs369811402	snp	A/G	2.1959e-05	0.00331346	intron-variant	RNF213	GRCh38.p7	17:80317148	TGTGCCGTGGCATTT[A/G]GTCGTGAGAGTGGGT	57674
rs369825556	snp	A/G	9.8894e-05	0.00703116	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381517	ACAAACCAGATCCCC[A/G]CTGAACACTCTGTTC	57674
rs369827804	snp	C/T	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80312956	GGTGCAGCATCTCGC[C/T]GGGAACCTGAGTCCA	57674
rs369855123	snp	C/T	5.032e-05	0.00501572	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372029	CTTTTGGAAACTATC[C/T]GAACCACATGGTTTA	57674
rs369872258	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359502	ACTCTAGCCTGGGTG[A/G]TGACAGAGTGAGACT	57674
rs369881425	snp	A/G	0.000131435	0.00810558	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351638	TGCTTGTTTTTGTGT[A/G]TGTGTTTGTTTTTAA	57674
rs369901699	snp	A/G	1.64846e-05	0.0028709	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364418	GAGTGAGTGAGTGGC[A/G]CCCTCTTTTGACAGA	57674
rs369902370	snp	C/T	0.000164875	0.00907801	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385206	GGACCAGGACTGTCC[C/T]GCATTTGGCGGTTCG	57674
rs369918247	snp	C/T	8.25403e-05	0.00642365	utr-variant-5-prime, intron-variant	RNF213	GRCh38.p7	17:80263644	CCAGCGACTCCTGCT[C/T]TTGCTTCTGGATCTG	57674
rs369925295	snp	A/C/G	1.69229e-05	0.00290881	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389361	TCAGACGATTCACGT[A/C/G]TTAAAGGTGGGTCTC	57674
rs369925564	snp	A/G	9.90573e-05	0.00703696	missense	RNF213	GRCh38.p7	17:80343161	GTGAAGAGGTTGCAC[A/G]ACAAAATGAAGATGC	57674
rs369930276	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389134	GAGATGCCAGAAACC[C/T]AGCCCACAGACATCC	57674
rs369933581	snp	A/G	4.94262e-05	0.00497098	missense	RNF213	GRCh38.p7	17:80346263	TCAGGGACGTGGAGC[A/G]CTGTGTGAAAGTTTT	57674
rs369940788	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314776	TGGAGGTGATGGTGG[A/T]GGTGGTGGAGGTAAT	57674
rs369944980	snp	A/G	9.92769e-05	0.00704476	intron-variant, missense	RNF213	GRCh38.p7	17:80319469	GCCAAGGGCAATGGC[A/G]CTGAAATCTAGTTCT	57674
rs369947979	snp	C/T	0.000115809	0.00760861	synonymous-codon	RNF213	GRCh38.p7	17:80348007	CGGCTACCACTCGGA[C/T]GCCTGCGCGTCTGTG	57674
rs369961411	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373952	AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	57674
rs369974574	snp	C/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80344477	AGTGATTTCCTGGCT[C/G]AGAACGCAGCTCCCA	57674
rs369984023	snp	A/C/T	3.37258e-05	0.00410633	missense	RNF213	GRCh38.p7	17:80346961	GACGATCCCGCCCCC[A/C/T]ACAAAAAGGTCGGCT	57674
rs370004365	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80333506	CGAGACCAGCCTGAC[C/T]AACATGGAGAAACCC	57674
rs370006505	snp	G/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360898	TCAAAGCAGTCTCTC[G/T]CCTCATGAGCATATT	57674
rs370030157	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323924	ACACAGTGCTCCATG[A/C]GTCTTGTATCCTGCA	57674
rs370055048	snp	C/T	4.95479e-05	0.0049771	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393530	ATCTTTGGATGACTT[C/T]GGAGAGAAGACTCCT	57674
rs370071100	snp	C/T	0.000185465	0.00962798	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390247	CAATGTTGTGCTGTC[C/T]CTCCTGTGATCTTCT	57674
rs370080097	snp	G/T	1.67077e-05	0.00289026	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375918	TCTCAGTATTTGGAG[G/T]GATTTTATTGAATAG	57674
rs370086524	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80262001	AGCCTGGGTGAAACT[-/GT]CAAACAAACAAAAAA	57674
rs370092120	snp	A/G	4.99713e-05	0.00499831	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376550	ACCATGGCGGTAAGA[A/G]TAGGCCACAATTCCA	57674
rs370104316	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298155	CGCCCTAGGCTGGGG[A/G]CTGAGGGAAGCCCTG	57674
rs370105315	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359506	TAGCCTGGGTGGTGA[A/C]AGAGTGAGACTCTAT	57674
rs370107861	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80312606	GGGACCCAGGTTTAC[C/T]TCCGGGTCAGGAGCC	57674
rs370119174	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295957	CACTCACTGTGGTCA[C/T]GTCAGTAGTTTTTCC	57674
rs370132483	snp	A/G	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80290743	GGTGAGCGTGTCTGT[A/G]GGCTTGGGAGGAATC	57674
rs370157580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358954	TGAGAAATTTCTGTT[C/T]TATCTCCACCCTCCT	57674
rs370166212	snp	C/T	0.000526732	0.01622	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381777	ACAGCACAACGGCAG[C/T]GCAAGCAGGCTCGCT	57674
rs370229431	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314500	TGGAGGTGATGGTGG[A/T]GGTGGTGGAGGTAAT	57674
rs370234454	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80286751	GCCCTCATCACACAC[A/C]ACCAGGTTTCAGGGG	57674
rs370235044	snp	C/G	1.69513e-05	0.00291125	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288220	CAGGAGGGGACCGGT[C/G]CCCCCACCTCTGCTG	57674
rs370237798	snp	A/G	6.97095e-05	0.00590338	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386850	ATTCAGCGGCAGATC[A/G]TCAGCCGCTTCCTCC	57674
rs370264898	snp	G/T	1.66095e-05	0.00288175	intron-variant	RNF213	GRCh38.p7	17:80290770	AATCCCTCAGGGAAG[G/T]CATAGGATGCCCAGC	57674
rs370265010	snp	A/C	0.000691825	0.0185858	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353693	TTCTTGGGACCTCCC[A/C]TTGTGCTGCTGGTGA	57674
rs370268515	snp	A/G	9.89544e-05	0.00703331	intron-variant	RNF213	GRCh38.p7	17:80319154	TGGAGCGCTGCATCC[A/G]AAAGCTCTGAAACCA	57674
rs370272936	snp	C/T	1.65168e-05	0.00287369	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369457	TTCTGTAAGGAGGCA[C/T]TTGGGAAACACCATC	57674
rs370275484	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80291304	ATCTTGCTCTGTTGC[C/T]TAGGCTGGAGTGCAA	57674
rs370276315	snp	C/T	0.000164897	0.00907861	synonymous-codon	RNF213	GRCh38.p7	17:80347482	GCTGACCAAAAACTA[C/T]GTGGCACTGCAGATC	57674
rs370281360	snp	A/C	1.64776e-05	0.00287028	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381609	TCTGCAGCAGCACAT[A/C]CTGAAGGACCTGGAG	57674
rs370296124	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398499	AGAGTGAAGCCTGGA[C/T]AGGTCCCTTGTTTCA	57674
rs370319556	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362562	AAAAACAACAGCCGC[C/T]GGCCAGTGCTGCAAA	57674
rs370320371	snp	C/T	0.000407339	0.0142655	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363591	CGCTCAGCCACGCCC[C/T]GCTGTCCGTCTCCCC	57674
rs370331413	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80346366	CAAAAATCACACCGA[A/G]AGAGATCCCGTCCTC	57674
rs370341809	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397447	GCACCACACCCTGGG[C/T]CTGGTAGTTAAAGAT	57674
rs370346019	snp	A/G	0.000300758	0.0122592	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373181	GTGAGAAGCGGGGCC[A/G]GGCAGCACACAAACA	57674
rs370354037	snp	C/T			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399267	TTCAGGAAAGGATGA[C/T]CTATGGTTCCTCCCA	57674
rs370354970	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80263180	AGCCTCCCCCCATTA[C/G]TAGGAATCTGACTGC	57674
rs370358024	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353952	ACCCTCATCGCATAC[A/G]GGCGGTTTGGCTTTT	57674
rs370361584	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80279045	AGGATGGGCGTTTTC[A/G]GGTCACCCTTGGGCT	57674
rs370367298	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324481	GATAAGGTTTTCTTT[C/T]ATCCTTTTAAATGTC	57674
rs370375142	snp	G/T			missense	RNF213	GRCh38.p7	17:80347254	GGCTTCAAATAGAAA[G/T]CCTTCCCCGCAAGAC	57674
rs370379930	snp	C/T	0.000149714	0.00865071	intron-variant	RNF213	GRCh38.p7	17:80349949	CTCTCCCTCCCCAGC[C/T]GCAGCCGTGTGGCTT	57674
rs370384141	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392997	GGAGCCTTTTTTTTT[-/T]GAGACAGGATCTCAC	57674
rs370384149	snp	A/G	8.25307e-05	0.00642328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364556	CTTACTAGACAAGGT[A/G]AGTACTTGGGCTGGC	57674
rs370387797	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314934	GTGGTGGTGAAGGTG[A/T]TGGTGGAGGTACTGG	57674
rs370395445	snp	C/G/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352382	AGCATGTAGGTCACA[C/G/T]GGCGTGGAGACTCCC	57674
rs370397913	snp	C/T	0.00014872	0.00862193	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380787	TGCAGCGTGCCAAAG[C/T]GGCCAGCCTCAGCCT	57674
rs370411986	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356102	CACCTCCTGGGTTCA[A/G]GCGATTCTCCTGCCT	57674
rs370416224	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324947	TTTCAGAAATGCTAT[C/T]GAGTAGGTAATTTGC	57674
rs370426640	in-del	-/TGGTGTCCAGCAACAGTGGCCACTCAG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365112	TCTGTGGCCACGCAG[-/TGGTGTCCAGCAACAGTGGCCACTCAG]CCAAACACAGCCTCA	57674
rs370427297	snp	A/C	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389920	GCGGCTGCACAAAGT[A/C]AGTCTGGTCTCTTCC	57674
rs370457110	snp	C/T	1.71507e-05	0.00292832	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354199	CCTCTTGCCCCTGCC[C/T]CCACGTGGGCTCTTC	57674
rs370461688	snp	C/T	6.59196e-05	0.00574068	intron-variant	RNF213	GRCh38.p7	17:80291608	TTTTGGATAGCCAAC[C/T]GTATCCTGTTCATTC	57674
rs370461742	snp	A/G	0.000581806	0.017046	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358258	TGGTTCCTCTGACCC[A/G]TGGTGGCCCATCTCT	57674
rs370463812	snp	A/G	0.000572246	0.0169055	missense	RNF213	GRCh38.p7	17:80339451	TTGTGACCCAGAAGC[A/G]AATGGAGCACTTTTA	57674
rs370465548	snp	G/T	1.71334e-05	0.00292684	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385495	TTTGGCCCTTTCAGG[G/T]GGTTGCTATCATACG	57674
rs370467413	snp	C/T	0.000609339	0.0174442	intron-variant	RNF213	GRCh38.p7	17:80343823	AACTCGCCATCGTGT[C/T]GTGTGTTTACACCTC	57674
rs370477255	snp	C/T	0.000158977	0.00891422	intron-variant	RNF213	GRCh38.p7	17:80340367	TGTTGGTAAGGAGAG[C/T]GGCAGGGTGGGCAGG	57674
rs370491274	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318723	GGACTACAGGCGCCC[A/G]CCACCGCGCCCAGCT	57674
rs370520790	snp	A/C/G	3.33084e-05	0.00408082	synonymous-codon	RNF213	GRCh38.p7	17:80273338	CCCGTGCTTGTTCCC[A/C/G]GGCTCAGACAGTTGG	57674
rs370523414	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375541	CCCGTGTCTACTAAA[A/G]GAAAAAAAAAAAGAA	57674
rs370523908	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314403	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGTGG	57674
rs370527198	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80292622	ATCTGTCAATAGACG[C/G/T]GGGCGCTTCCCTTCT	57674
rs370535858	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80309051	GTCACCATCCTACCT[A/G]ACTGTGTGTCTGAAA	57674
rs370576785	snp	A/G	0.000461696	0.0151867	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369492	TGTCTTCTGTTTCTC[A/G]TGTTCTAAGGGAAGC	57674
rs370607351	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80278950	AGAATGCTCCCTGCC[C/T]TGGTGCATGCTGGCA	57674
rs370621924	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331019	AGATGGGATTTCATC[A/G]TGTTGGCCAGGCTGG	57674
rs370634100	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365118	GCCACGCAGTGGTGT[C/T]CAGCAACAGTGGCCA	57674
rs370653889	snp	C/G/T	0.000181697	0.00952984	missense	RNF213	GRCh38.p7	17:80317222	AAATCCAATTCCCCG[C/G/T]GGAGCATGGCTGGAA	57674
rs370670026	snp	C/T	2.65094e-05	0.0036406	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372508	CTTTTCTTTCTTGTT[C/T]CTTGTTCCTCAGGAT	57674
rs370685808	snp	C/T	3.36005e-05	0.00409867	intron-variant	RNF213	GRCh38.p7	17:80295523	GTGAATTCAAGTCCA[C/T]GGTTCATGCATCTTC	57674
rs370692450	snp	A/G	0.000300616	0.0122563	missense	RNF213	GRCh38.p7	17:80289743	GAGCCTGAAGACCTC[A/G]AGAAGCCAGAGGGGA	57674
rs370699905	snp	A/C/T	0.00128365	0.0253021	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372640	CCGAGAGCCTGCCAA[A/C/T]GAGGCCTCGGTTGAA	57674
rs370755934	in-del	-/GAGTCCCTCCT			intron-variant	RNF213	GRCh38.p7	17:80308473	TTCTGAGTCCCTCCT[-/GAGTCCCTCCT]AAGCCTCCTCCTAAG	57674
rs370757499	snp	A/C	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80306336	CTGGTTTAGTCTGCT[A/C]CCTCTGAGTCACCTG	57674
rs370767936	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80332025	CTTTGGAGTGCTTGC[A/G]GTAAGACACTCACAA	57674
rs370775607	snp	C/T	0.000100612	0.00709196	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390221	TGCACACCTATGGGG[C/T]GGGGCAGACACAATG	57674
rs370780815	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393708	CATACATGTTCTGAA[A/T]CTTTCTCATCATTTT	57674
rs370784460	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80312121	TTACAGAGTGAGACT[A/C]TGTCTCAAAAAAAAG	57674
rs370797336	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80271600	AGAGGTGGGGTCGTC[C/T]AGACCCAGGATTGAA	57674
rs370806897	snp	A/G	0.0217236	0.101931	intron-variant	RNF213	GRCh38.p7	17:80266430	GAAGAAAAGAAAAGG[A/G]AAAAAAAAGCCTTAC	57674
rs370812805	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367322	TGTTTTGTTTCTCTA[A/C]AAAATGATCTATCGC	57674
rs370815214	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80315185	GGTGATGGTGGTGGA[C/G]GTGATGGTGGAGGTA	57674
rs370819113	snp	A/G	8.41687e-05	0.0064867	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354005	ACGGATGACCCAACC[A/G]TCTCCACCAACAGGT	57674
rs370832733	snp	C/T	3.52473e-05	0.0041979	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385651	CCCTGTACCACTAAG[C/T]GTTCCAGGAGAGCCT	57674
rs370836301	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381752	GGGGCAAGGGCTGGG[C/T]GGGGATCACACAGCA	57674
rs370841241	snp	C/T	0.000385134	0.0138715	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373027	CAAGCAGTTCTGTAT[C/T]CGGGTGGAGAACGAC	57674
rs370842925	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80313769	GGAGGTGGTGGAGGT[A/G]CTGGAGGTGATGGTG	57674
rs370862777	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287604	CCGAGTGTGGCGAGC[A/G]CTTCAAGGCCACTTG	57674
rs370866882	snp	A/G	1.672e-05	0.00289132	synonymous-codon	RNF213	GRCh38.p7	17:80350313	CAGAAACTGTTTAAC[A/G]AATACAGCCAAATGT	57674
rs370868819	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80286205	GGGTTGGTGTCGGAC[A/G]CAGGCCGGTGTTGGA	57674
rs370876601	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80262967	GTGTGCCCTGAGGCT[G/T]CTTACTGGGGAGGGA	57674
rs370878729	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80292800	CTTCCCCTCGCTCCC[C/G]CTCCCTGCACAGTGA	57674
rs370917414	snp	C/T	0.00755907	0.0610114	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391994	GCTGGTCTCGATCTC[C/T]TGACCTCAAGTGATC	57674
rs370927428	snp	C/G			missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385597	TCCACATGGAACAAA[C/G]TGAGGAGATCGCTTG	57674
rs370932670	snp	A/G	3.29478e-05	0.00405867	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385144	GAATACAGCTCCATC[A/G]GAGGCTTCCTCAGCA	57674
rs370934396	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314514	GTGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs370939163	snp	A/G/T	0.0143541	0.0835	synonymous-codon	RNF213	GRCh38.p7	17:80325164	AAAGCATCTGCTCAC[A/G/T]TTGGCAGATGTCAAG	57674
rs370942731	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80300711	GGCACCCCACCATGC[C/G]TGGCTAATTTTTGTA	57674
rs370959441	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381420	CCTGGATCACTCCGC[C/T]GTTTTCATCTTAGAA	57674
rs370966572	in-del	-/T	0.488905	0.0736498	intron-variant	RNF213	GRCh38.p7	17:80333227	CTAATTTTTTTGGTA[-/T]TTTTTTTTTTTTTTA	57674
rs370993666	in-del	-/TGTGCGCGTGTGTG			intron-variant	RNF213	GRCh38.p7	17:80290494	GTGCGCACGTGTGTG[-/TGTGCGCGTGTGTG]CATGCACATGGCAGG	57674
rs370995636	snp	C/T	0.000510528	0.0159688	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389958	TGGACAGAGGGACTG[C/T]GCTCCCTTCTCCCTG	57674
rs371023146	snp	A/G	1.64947e-05	0.00287177	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361903	GGTAGATGTTTAGAT[A/G]CTGGCTAAGGGTCAG	57674
rs371028020	snp	C/T	3.29468e-05	0.00405861	missense	RNF213	GRCh38.p7	17:80294885	TGCAGACCTGGGACA[C/T]CATCAACCTGAACAG	57674
rs371042188	snp	A/G	2.18763e-05	0.00330722	intron-variant	RNF213	GRCh38.p7	17:80343342	TAAGTGCCCTCCAGC[A/G]TCAGCCGATGGCCAC	57674
rs371045041	snp	A/C/G/T	0.000115448	0.00759693	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386749	GTTATGAAGTGGAGC[A/C/G/T]GGACCTGACTCCACT	57674
rs371045342	snp	A/G	1.65141e-05	0.00287346	missense	RNF213	GRCh38.p7	17:80348267	CGGCAGACCTGGAGC[A/G]CCACGCCATCTTCAC	57674
rs371056932	snp	C/T	0.000274601	0.0117143	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353486	CCTTCTGAGTGGTAA[C/T]GCAATCACGTTTGCT	57674
rs371080115	snp	A/G	8.24477e-05	0.00642005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364509	GAGAGCCGCGTCCCC[A/G]AGTTACAGGGGCTGG	57674
rs371081740	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387953	TGTGAGAGCCCATGG[-/A]TTTTTTTTTTTTTTT	57674
rs371084300	snp	C/T	8.30558e-05	0.00644368	intron-variant	RNF213	GRCh38.p7	17:80312976	ACCTGAGTCCACAGC[C/T]GAGGATGACTGACCC	57674
rs371091011	snp	A/G	8.23839e-05	0.00641757	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358336	CACCCCTCTGCTGGC[A/G]AGCATGATATCATTC	57674
rs371096422	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298225	GCTCCTCTTGCTCTG[C/T]GTGCACGGTGCTTGC	57674
rs371096537	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80269670	TCAATCTATCCATCC[A/T]TCCATTCATCTGTTC	57674
rs371107957	snp	C/G	0.0013082	0.0255419	intron-variant	RNF213	GRCh38.p7	17:80273435	CGGCTCCCCTCCGCC[C/G]CCGCTCACTCTGCCC	57674
rs371111495	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325763	TTAGAGTCCAGTTGG[C/T]GTGTGAGACCTTAGA	57674
rs371120165	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80309955	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	57674
rs371125777	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80284608	AGCTCCACCTTTCTA[A/G]TCCCATTGAGGAAGT	57674
rs371134969	snp	A/G	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389788	ATGAGTGGGGGTGTG[A/G]GACCTCAGCCCCCAC	57674
rs371139159	snp	A/G	6.68639e-05	0.00578165	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373077	TGCGGAAGCTCAGCA[A/G]CCAGCGGGGGATGGA	57674
rs371157113	in-del	-/AC			intron-variant	RNF213	GRCh38.p7	17:80281626	ACACCACTCACACAC[-/AC]CCCCAACACACACTC	57674
rs371164542	snp	C/T	0.000100002	0.00707042	synonymous-codon	RNF213	GRCh38.p7	17:80346540	TCTTTTTCTGGACGG[C/T]GTACCTCTGAGGAAA	57674
rs371167617	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315856	GTGGTGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs371177210	snp	A/G	1.65091e-05	0.00287303	missense	RNF213	GRCh38.p7	17:80348149	GTGGTCCGGCTGAGC[A/G]CCTACTCGCTGGGCG	57674
rs371179291	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315015	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs371187357	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270098	AGACATCTCCTCTGC[A/G]TGAATGTGTGCGCAC	57674
rs371195005	snp	C/T	0.00105423	0.0229347	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354165	GGATGACGCGTGCCA[C/T]GGTATGAGCCTCCCC	57674
rs371202144	snp	C/T	3.29516e-05	0.00405891	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369594	TCAAGGACAACGCTC[C/T]GCCTGAGAAGGAAGT	57674
rs371206834	snp	C/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80335066	AGCTGGGATTACAGG[C/T]GCCCGCCACCACACC	57674
rs371223052	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319080	AGCTTAAAATTGGGG[A/G]AAACAGTAAAACAGC	57674
rs371224096	snp	C/T	0.000437904	0.0147905	stop-gained	RNF213	GRCh38.p7	17:80332503	GATTGGATCAAGGAC[C/T]GAGTCGAACAGATCA	57674
rs371228064	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305392	CATGTTGGTCAGGCT[A/G]GTCTTGAACTCCCAA	57674
rs371229233	snp	C/T	6.83535e-05	0.00584569	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363830	CTGCTTCATCTGGCG[C/T]GCGCTCACCAGGAGC	57674
rs371238281	in-del	-/TTA/TTTA	0.256684	0.270807	intron-variant	RNF213	GRCh38.p7	17:80276093	TTATTTATTTTTTGT[-/TTA/TTTA]TTTATTTATTTATTT	57674
rs371269722	snp	C/T	0.000197821	0.0099434	intron-variant	RNF213	GRCh38.p7	17:80307097	TGTGATTCAATCTTT[C/T]GTCCTGTTTTTCTTT	57674
rs371322122	snp	A/G			missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287972	ACAGCCAAGCCCAGC[A/G]GAGTGGCCCCACTGG	57674
rs371333913	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80293119	CTGGAGTGCAGTGGC[A/T]CGATCTCGGCTCACT	57674
rs371342247	in-del	-/TG	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80294274	CCTTCCTCCAGGGGC[-/TG]TGTCCCGTTCCTAGT	57674
rs371352709	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329092	GGAACCTGCCAACCC[C/T]GGGCTGCAGACGTAG	57674
rs371364731	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80289236	GGCACTGGAAGGTCC[C/T]GAGCGGGGAAGGGTC	57674
rs371366637	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80276874	TGGCCAACATGGTGA[A/T]ACCCCGTCTCTACTA	57674
rs371383693	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370315	TGACATCCAAGAATA[G/T]TATCACCTGTGGTAC	57674
rs371396094	in-del	-/ACAA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383512	TACATCTATAAACAA[-/ACAA]CACTGAAATTAGAAG	57674
rs371407824	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80290704	CAAAATGGGACAGCA[A/G]TATCTGTGAGCTGCA	57674
rs371433961	snp	A/G	0.00380111	0.0434293	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375864	AAGCCTCCACCCCAC[A/G]CCAGAGGTGAGTAAC	57674
rs371439947	snp	A/G	0.00011458	0.00756816	missense	RNF213	GRCh38.p7	17:80337691	ATCAACCAAAGAGGC[A/G]TCTATGTGATCCAGG	57674
rs371441113	snp	A/C/G	0.000545878	0.0165121	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386819	AGAGACCGTGCAGGA[A/C/G]TTCGATCTGGAGAAG	57674
rs371450557	snp	C/T	0.00161506	0.0283711	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369713	AGCCCCTCATTTCTT[C/T]ATCTCGCTTCTGCAT	57674
rs371458237	snp	G/T	4.95888e-05	0.00497915	missense	RNF213	GRCh38.p7	17:80348036	TGGTGCTGCAGGTCA[G/T]AGAGAGGCAGGGTCC	57674
rs371459747	snp	C/T	3.3222e-05	0.00407553	synonymous-codon	RNF213	GRCh38.p7	17:80347347	TCTGGCCAATTTGCC[C/T]GAGGCCAAGTGCTCA	57674
rs371464599	snp	A/G	1.66643e-05	0.0028865	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363647	GGCCTGCACGGAGAT[A/G]CTGACAAGAAACACC	57674
rs371467373	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80333339	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	57674
rs371474627	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80281558	TCACACACCCCCCAA[C/G]ACAAACGCCCCACTC	57674
rs371475461	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80292001	CTGACTCTGGGTTGT[A/G]TCTCTGGTTGGTTAA	57674
rs371481300	snp	C/G	0.000472263	0.0153593	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383645	AGCAATACCTCACTT[C/G]CAGAATTTTTTTTTT	57674
rs371498826	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320036	GTTGAGATATTGTTC[A/G]TATGCCATACGGTAC	57674
rs371517262	snp	A/G	0.00018389	0.00958702	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376560	TAAGAGTAGGCCACA[A/G]TTCCATCGGCCTTCA	57674
rs371526557	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80306157	AATCATTTTTGAATT[C/T]GGGACTGTTTCTGTC	57674
rs371533852	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377055	CGACTTGGGGTCCAC[A/G]TGGTTTGTGCCTCAG	57674
rs371547532	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379667	TGACTGCCATGCGCC[A/G]ATTGGAGGCATTGAC	57674
rs371554385	snp	C/T	1.69424e-05	0.00291048	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288244	TCTGCTGGTGAAGGC[C/T]ATTCTAGGACTGAAG	57674
rs371556089	snp	C/T	0.000132	0.00812297	missense	RNF213	GRCh38.p7	17:80313085	GGACCCTTGCTGCTA[C/T]GAAAAGGTGGCTCCG	57674
rs371556761	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80314609	GGAGGTGATGGTGGT[G/T]GTGGTGGTGGTGGTG	57674
rs371559000	snp	C/T	3.30743e-05	0.00406645	synonymous-codon	RNF213	GRCh38.p7	17:80313038	ACAGAGAGATGAAAC[C/T]GGAAATAATTCAGTC	57674
rs371571722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387703	CATATGGGATAAAGC[C/T]GACACTCTGTTGTCT	57674
rs371575527	snp	C/T	3.29516e-05	0.00405891	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358398	CCAGGCCAGATACTC[C/T]GCCCTGGGCAAGAGA	57674
rs371598729	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80328313	GGTTACTTTATTGGT[C/G]TTCTTATTTTCCAGG	57674
rs371607465	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357104	GTATTTTTAGTAGAG[A/G]CGGGATTTCACCATG	57674
rs371619739	snp	A/G	0.000280101	0.011831	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380881	TGGGCAACCCGCAGC[A/G]GAGAGACGTGGTGAC	57674
rs371629445	snp	A/G	0.000712843	0.0188657	synonymous-codon	RNF213	GRCh38.p7	17:80339821	TGGGTCTCCCGTGGA[A/G]CGTTGTCTCCCGAGA	57674
rs371638730	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377633	ACTTAACAAATTAGC[A/G]TGGGATGCTCTGGAC	57674
rs371640051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377864	TGGAGGAGGGGGATC[A/G]TGGGTCAGGAGAGTG	57674
rs371672780	snp	A/G	1.71026e-05	0.00292421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363577	GGTGGGAGGGGCACC[A/G]CTCAGCCACGCCCTG	57674
rs371676448	snp	C/T	6.58979e-05	0.00573974	missense	RNF213	GRCh38.p7	17:80345647	CTTAGCGACCTGCGG[C/T]GTGGTGGTACCAATG	57674
rs371693850	snp	A/G	0.000181247	0.00951792	intron-variant	RNF213	GRCh38.p7	17:80344657	TCTTGTAACCATTTC[A/G]TTAATGTCTCTCCTT	57674
rs371695657	snp	A/C/G/T	4.94275e-05	0.00497111	intron-variant, missense	RNF213	GRCh38.p7	17:80319326	AGGTGAACAATCTCT[A/C/G/T]CTCCTGGGAAACGGA	57674
rs371696654	snp	C/T	4.95119e-05	0.00497529	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389149	CAGCCCACAGACATC[C/T]CTCTCCTGCTTTTCA	57674
rs371701458	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328195	AATGGCCATCTCGAA[A/G]AAGTGGGTATGCGCA	57674
rs371727715	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349230	ATGATGTCCGCCGGG[A/G]ACAGGTTTCTATGCA	57674
rs371735506	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80264509	ACCCTAAAACTAGCA[A/G]CCCCCAGACCTTCAG	57674
rs371750093	snp	A/G	3.29516e-05	0.00405891	synonymous-codon	RNF213	GRCh38.p7	17:80345922	CAATCCATACCGGAA[A/G]CACTCTGAGGAGATG	57674
rs371765632	snp	C/G	4.94214e-05	0.00497074	intron-variant	RNF213	GRCh38.p7	17:80291623	CGTATCCTGTTCATT[C/G]ACAGAGACTTGGGTC	57674
rs371768403	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80341665	ATCGCTCCAGCCCAA[C/G]AGGTCGAGGCTGTGG	57674
rs371775471	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80289999	TAGGAGGTGGAGGGG[A/G]GTGGGCACCTGTGCC	57674
rs371788270	snp	A/G	3.29533e-05	0.00405901	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374439	CATTGTTCACCCCCA[A/G]CTAACCTCTGTATTC	57674
rs371796519	snp	A/G	3.29679e-05	0.00405991	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386390	CGCCTACACAATGAA[A/G]TTGTCTACGCCGTGG	57674
rs371808595	snp	A/G	0.000181598	0.00952711	intron-variant	RNF213	GRCh38.p7	17:80313182	GGTAGGCATTTGGCC[A/G]AAGGCTTCTGGGTAG	57674
rs371811198	snp	C/T	1.68289e-05	0.00290072	synonymous-codon	RNF213	GRCh38.p7	17:80346948	CGGATGCATTGAAGA[C/T]GATCCCGCCCCCCAC	57674
rs371814872	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317087	TTCGCGGAGTCCCGC[A/G]CTCTCTGTATTGCCG	57674
rs371853290	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80303567	TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	57674
rs371874765	snp	C/T	3.31978e-05	0.00407404	missense	RNF213	GRCh38.p7	17:80350368	TTTGAAGATGGAATC[C/T]GTAGCGCCCAGCTCA	57674
rs371880091	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357106	ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT	57674
rs371887862	snp	C/G	4.94996e-05	0.00497467	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380827	GTTCTCTCGTTCTTT[C/G]CAGAGACAAGGCAGA	57674
rs371905368	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357204	TTAGACGTGAGCCAC[C/T]GTGCCCAGCCACCTT	57674
rs371927175	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326142	TATTTAATTTTAAAA[A/C/T]AAGGTCTTCTCTGTT	57674
rs371930100	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80314329	AGGTAATGGAGGTGA[-/TGG]TGGTGGTGGTGGTGG	57674
rs371930676	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80317541	TTCCTGACCCCTTCG[C/T]TGGACTTGCGACAGG	57674
rs371935395	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310836	GGATTACAGGCATGA[A/G]CTACTGCACCCGGCT	57674
rs371937334	in-del	-/GT	0.0154538	0.0865337	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365583	ACGCCACACCAGCTC[-/GT]GTCTCGTGGTCCTAA	57674
rs371941801	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366138	AGGCTTGGGGGAAAG[C/T]CCTGCCTTCCGCCGT	57674
rs371953227	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80286245	AGCGGGAGGCTGGAG[C/G]CAAGCTGTGGCCTGG	57674
rs371956375	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352079	TAGATGGTCTCAATC[C/T]GTTGACCTCATGATC	57674
rs371959759	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80334590	ATTTTTACTGGAGGA[C/G]AAGGAGAGTTCCTGC	57674
rs371962490	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281088	CACCCCCCGCCACAC[A/G]TACCCCACTCACACA	57674
rs371971780	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80265083	AGTTTTTTTGTTCTT[G/T]TTGCTCTGGCTAGAG	57674
rs371978343	snp	C/T	0.000437904	0.0147905	missense	RNF213	GRCh38.p7	17:80339547	GTGATGCCGCCCTAA[C/T]GATGCTATCCTTCAT	57674
rs371989481	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314553	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs372001577	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287590	CGGCCGTGACCGTGC[C/T]GAGTGTGGCGAGCGC	57674
rs372016811	snp	A/G	0.000131828	0.00811768	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367781	GACGTGAAGACGCAC[A/G]GGCCTTTTGAGGCCG	57674
rs372020320	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383872	TACCTCCAGCACATT[A/G]TGGAACAGAAAAATG	57674
rs372036678	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268355	GAGACCCTGTCTCAG[A/G]AAAAAAAAAAAAAAA	57674
rs372046687	snp	A/G	0.000479946	0.0154836	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381007	AACCCAGTGCTGCCA[A/G]ACAATGGGCTCAGTT	57674
rs372075469	in-del	-/AT			intron-variant	RNF213	GRCh38.p7	17:80269524	CTATCCATCCATCCT[-/AT]CTTTCTATTCATCCA	57674
rs372084531	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382669	TGGCAGCAGCTGAGA[C/T]GGCTGGCGGTAGCCT	57674
rs372087376	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80295784	TGAGTTTCACCGTGA[C/T]CTAAGCCACATCCTT	57674
rs372093859	snp	C/T	3.42472e-05	0.00413792	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373152	TGTTTCCCAAGGACG[C/T]TGTCAAGCAGCAGGT	57674
rs372098453	snp	C/T	0.000132253	0.00813075	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353037	CATCAGCCAGCTGTT[C/T]GCGCCCGGAGACTTG	57674
rs372117379	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315429	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs372119103	in-del	-/TATC			intron-variant	RNF213	GRCh38.p7	17:80268726	TCCATCTTATCTATC[-/TATC]CTATCTATCCATCTA	57674
rs372119242	snp	C/T	4.97772e-05	0.0049886	synonymous-codon	RNF213	GRCh38.p7	17:80295610	GGTACCATTGCCGGA[C/T]GGAAAAAGCACGGAC	57674
rs372132185	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392953	GAAAAAGTAACATGA[A/G]GGGACTGATTGGTCC	57674
rs372136414	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371262	TATCACTGTGGGCAC[A/G]GCATTAAGGAATAAT	57674
rs372156192	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80295096	GACTCTGTGGGCCAG[A/G]TTGCAAATGGGAATG	57674
rs372187734	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80264310	GCCTGGGTTAGTTTT[G/T]GAGGGGCCGTGAGGG	57674
rs372193582	snp	C/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383736	AGATAAGCGTATCAG[C/G]TCTAACCCTGTGGCC	57674
rs372211904	snp	A/G	0.000164813	0.00907629	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354468	GGGTATCCAAGATGC[A/G]CCTCAGTGTCTTTTT	57674
rs372219169	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80296386	TGCGCGTGTTTAGGA[C/G]GTTGTGGCGTGACGC	57674
rs372260408	snp	A/G	0.00150949	0.0274311	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288410	GGCACTGAGCCCTCG[A/G]CACCTGGGCTCTGCT	57674
rs372275199	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322680	TTGGCCTTCCAAAGT[A/G]TTGGGATTGAAGGCA	57674
rs372281577	snp	C/T	0.000875616	0.0209055	synonymous-codon	RNF213	GRCh38.p7	17:80336162	CTTCTCTTCCCCAGG[C/T]ATCAATGAGCTGAAG	57674
rs372286385	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387253	TGAGATCACAAGTGT[A/G]CACCACCATGCCCAG	57674
rs372291378	snp	A/C/T	0.000558328	0.0166991	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363598	CCACGCCCTGCTGTC[A/C/T]GTCTCCCCAGACCCT	57674
rs372291787	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365794	GTCTCATCATGTCTC[A/G]GCGCTCTGGGAGATG	57674
rs372294598	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388723	ATCCTGTGCACGGGG[C/T]TTTCTGCCTTCTCAG	57674
rs372296481	snp	A/G	1.64749e-05	0.00287005	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288723	ATGAAACAGCCACCA[A/G]CAACCACTCCTCCTT	57674
rs372309318	snp	A/C/G/T	0.000971211	0.0220166	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367714	CCCTCAGCCCTCCCC[A/C/G/T]CTGCTAATGACTCCT	57674
rs372312610	snp	C/T	0.000123464	0.00785601	intron-variant	RNF213	GRCh38.p7	17:80337541	GGAGAAGGGCAAGAT[C/T]CTCGCTCCAACCGTG	57674
rs372341055	snp	A/G	3.8578e-05	0.00439176	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372778	GGGTTTAAAGACTCC[A/G]TTATTTAGAAATTCA	57674
rs372365606	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287268	TGGGAGGCCGAGATG[A/G]GCAGATTGCCTGAGC	57674
rs372376812	snp	A/G	0.000165003	0.00908153	synonymous-codon	RNF213	GRCh38.p7	17:80263696	CATGGAGTGTCCTTC[A/G]TGCCAGCATGTCTCC	57674
rs372384213	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390046	GTTCAAGGTACAAAG[C/T]GGATCTGAGCCCGGA	57674
rs372397321	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80313909	TGATGGTGGTGGTGG[A/T]GGTGATGGTGGAGGT	57674
rs372399096	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80293420	GCTTTGAAAGAATAG[A/G]CATTAGTCCGGTAAT	57674
rs372461542	snp	C/G/T	3.29529e-05	0.00405901	intron-variant	RNF213	GRCh38.p7	17:80308998	CTTGCCGGGATTTCT[C/G/T]TTAACTCTTTGCGGG	57674
rs372470626	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265382	ATAATAGTGCGGAGA[C/G]CACTGGTAGTGCGCA	57674
rs372522813	snp	A/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381631	GACCTGGAGCAGTTG[A/G]CCAAGATGCTGGGAC	57674
rs372549930	snp	C/G/T	0.000447991	0.0149602	intron-variant	RNF213	GRCh38.p7	17:80289885	CCCTGCCTGAGAGCC[C/G/T]GGCACACCCTCTCCC	57674
rs372570711	in-del	-/AAC	0.00517822	0.0506191	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398819	ATACAAGTAGTTAGA[-/AAC]AACAACAACACTGTA	57674
rs372582199	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384360	GAGTGGGTGTGTGCC[A/G]GCGGTGCTGGGGTAC	57674
rs372585280	snp	A/G	1.6473e-05	0.00286988	splice-acceptor-variant	RNF213	GRCh38.p7	17:80343856	GCGATTCTGTTCTTA[A/G]GTGCAGACTGGAATT	57674
rs372587102	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392584	GGTCATTGACCTTAA[A/C]CTGCTCCTCAGGATT	57674
rs372587554	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320679	ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCGAGCA	57674
rs372590789	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80262021	ACAAACAAAAAATGC[C/T]TTTTGGAGGATTTTT	57674
rs372618476	snp	A/G	3.30371e-05	0.00406417	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386663	ATGCCTGGCCTGGAC[A/G]CTGAGCGCTGTCTTT	57674
rs372639743	snp	C/T	0.0011387	0.0238339	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369472	TTTGGGAAACACCAT[C/T]CACCTGTCTTCTGTT	57674
rs372675937	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378843	ATTTTGAAAAATAAG[C/G]CTTTGGAAGTAGATT	57674
rs372677556	snp	C/G/T			intron-variant	RNF213	GRCh38.p7	17:80337553	GATCCTCGCTCCAAC[C/G/T]GTGGCCCGTGTTCTC	57674
rs372679963	in-del	-/ACAC			intron-variant	RNF213	GRCh38.p7	17:80281401	ACTCACACCACTTAC[-/ACAC]CCCCAAGACAAACAC	57674
rs372689047	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397717	TCTTGCCGAAGCGCC[C/T]GGCTGAATAAAGCCC	57674
rs372690068	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314997	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs372690213	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80313770	GAGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs372692504	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378438	TGGGTTGAGCTGACA[C/T]GTGGTAGTTAGTTAT	57674
rs372700213	snp	A/G	1.65594e-05	0.0028774	missense	RNF213	GRCh38.p7	17:80306449	GGCTTCCGGGACTTG[A/G]GCAAGTCTTGAATAC	57674
rs372704782	snp	A/G	0.000598524	0.0172888	missense	RNF213	GRCh38.p7	17:80346515	TGGATGAAATAACAC[A/G]GGCACAGGATCTTTT	57674
rs372715025	in-del	-/AG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374149	CCACCTGGGGTTTAG[-/AG]TTGACATGACTTGAG	57674
rs372722051	snp	A/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80291671	GAAGGCATTGTCTGC[A/G]TTTCCAAGAAGCACC	57674
rs372755445	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80303388	GAGACGCCCCCTCAT[A/G]AAGCATGATGCTCAG	57674
rs372759772	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80275852	TATTTTTGGTAGAGA[C/T]GGGGTTTCACCATGT	57674
rs372775492	snp	A/G	1.65135e-05	0.00287341	missense	RNF213	GRCh38.p7	17:80347918	GAGCTCTGTGCGTGG[A/G]TGGAGAAGTTCATCA	57674
rs372791334	snp	C/T	0.00016472	0.00907375	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376369	TGATATCAGCCGTTT[C/T]GCAACATCGCTCGTG	57674
rs372793187	snp	C/T	3.30929e-05	0.0040676	intron-variant	RNF213	GRCh38.p7	17:80344031	GTCTGTACTGTGGGG[C/T]GTTTTCGCCTGGCGT	57674
rs372805247	snp	A/G	4.95446e-05	0.00497693	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352896	GGCTGAGCAGCAGCC[A/G]GGAAAGACACAAAGA	57674
rs372809375	snp	G/T	0.000153988	0.00877328	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367753	CTTTCTTCAGTGTCT[G/T]CGAGAGAACTCTGAC	57674
rs372811936	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393270	ACACACGTGAGCCAC[-/A]CAGTGCTGGGCTTAC	57674
rs372813392	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80338958	ATCTCAAAAAAAAAT[A/T]AAAAAAAAAAAAAAA	57674
rs372829933	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378697	TTTTTCTGAGCTTCA[A/G]TCACTTCCTTGTCCA	57674
rs372831621	snp	A/G	1.65822e-05	0.00287938	synonymous-codon	RNF213	GRCh38.p7	17:80295652	GGACTGCCCAGTGAG[A/G]AGTAAACTGAAAACA	57674
rs372856428	snp	C/T	1.64784e-05	0.00287035	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380880	CTGGGCAACCCGCAG[C/T]GGAGAGACGTGGTGA	57674
rs372880107	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341608	CCAGGCATGGTGGTG[C/T]ATGCCTGTGATCCCA	57674
rs372882150	in-del	-/A	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80293377	AACATGATTTTTACT[-/A]GCTAGAGAGTGTACT	57674
rs372898507	snp	A/G	6.65546e-05	0.00576827	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386457	AGCCACCAGGAAGTG[A/G]TGCCTGCTCAGCCCA	57674
rs372913538	in-del	-/TAGGTTGGTGGGAGGG			intron-variant	RNF213	GRCh38.p7	17:80271124	AGGTTGGTGGGAGGG[-/TAGGTTGGTGGGAGGG]GCAGGCTCAGAATCC	57674
rs372932832	snp	A/C/G	0.0016185	0.0284012	missense	RNF213	GRCh38.p7	17:80339750	CCTGCCTTCCTGCCC[A/C/G]ACTGCCTCGACCTAG	57674
rs372936859	snp	C/T	1.66294e-05	0.00288347	intron-variant	RNF213	GRCh38.p7	17:80273229	TGACCCTTCCTTCAT[C/T]TGCCGTTACAGATTC	57674
rs372946741	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80348765	TGGGGAAGAATGGCC[A/G]GGAAGGGATTGTAGG	57674
rs372953146	snp	C/T	0.000558334	0.016699	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372953	CACCAGCCACTCACC[C/T]GCTTTCTCGTTGGCC	57674
rs372981115	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80283544	CCTGCCTCCAGCCTC[A/C]CCGGGCTCTGCCCAA	57674
rs372998905	snp	C/T	3.60046e-05	0.00424276	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372547	TGAGAAGACCAGTGC[C/T]TACTCCAGAAATGAT	57674
rs373010567	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281537	CACATGCCCCACTCA[C/T]ACCACTCACACACCC	57674
rs373021348	snp	C/T	0.000364836	0.0135013	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353068	CCTGAGCGTGAGTCA[C/T]GAGGCGGAGCCCCTG	57674
rs373038505	snp	A/G	3.33979e-05	0.0040863	intron-variant	RNF213	GRCh38.p7	17:80291848	TCGTGGCAGCAGGCT[A/G]TCTGCTCACCCCTCC	57674
rs373045873	snp	C/G	4.94531e-05	0.00497234	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381500	GGCTCACCATCTTCT[C/G]TACAAACCAGATCCC	57674
rs373055730	snp	C/G	1.80853e-05	0.00300705	synonymous-codon	RNF213	GRCh38.p7	17:80317232	CCCCGCGGAGCATGG[C/G]TGGAAGGAGTCGTTG	57674
rs373059930	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314790	GTGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs373074337	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80271378	GGGAAAAAGGTCTGC[A/G]TGGTCCCTGCCCTCC	57674
rs373075310	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318298	GATAGAGGTTCTCAC[-/T]TTGGGCCATGGGTTT	57674
rs373081225	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80275567	AAAGACCTGAGAAGA[C/T]CTCAGTGCAGGCTGG	57674
rs373081355	snp	C/G/T	0.000736963	0.0191821	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288047	GTGACGGCCTCTCCG[C/G/T]GCCCACCGAGGTTGG	57674
rs373091232	snp	A/G	1.65343e-05	0.00287521	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374572	TGCAAGCCACTGGGC[A/G]TTAAGACTGCTCTGA	57674
rs373122840	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318655	CTCGGCTCACTGCAA[A/G]CTCCGCCTCCCGGGT	57674
rs373133054	snp	C/G	0.00045057	0.0150027	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353479	TGTGCCACCTTCTGA[C/G]TGGTAACGCAATCAC	57674
rs373144473	snp	C/T	0.000245864	0.0110847	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389381	AGGTGGGTCTCACAC[C/T]GAAAAGGAAATCAGC	57674
rs373152716	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80278620	AGACGGTGCTGGGAA[A/G]CTGGTCAGTGCCCAC	57674
rs373152877	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80291559	TTGCACTCCATGCTA[C/T]GTTTGAGAATAACTA	57674
rs373154701	snp	A/G	0.000116475	0.00763048	synonymous-codon	RNF213	GRCh38.p7	17:80332433	TGTGAATAAATACAC[A/G]GACCTGGATTCAGAA	57674
rs373156000	snp	C/G			missense	RNF213	GRCh38.p7	17:80345183	TGGTCACCATGGATG[C/G]GGTTAGGGAAGAAGA	57674
rs373161624	snp	C/G/T	6.59363e-05	0.00574146	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364459	GTCGGATTTTCTCCA[C/G/T]CGCACTCTTCGTGGA	57674
rs373166048	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80313619	GGAGGTGATGGTGAT[G/T]GTGGTGGAGGTGATG	57674
rs373175080	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80327072	CTCTTTGCATATGCT[A/G]TGAAAGTGTCTCCCT	57674
rs373184907	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80338926	GCACTCCAGCCTGGG[C/T]AACAATGCAAGACTC	57674
rs373216329	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392572	TTCAGGAGCTCAGGT[C/T]ATTGACCTTAAACTG	57674
rs373219568	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372489	TGTTTAAAAAAATAA[C/T]ATCCTTTTCTTTCTT	57674
rs373243379	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314190	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs373243959	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288453	CGTTGCTTCCCTGCC[A/G]GGGGGAGGGGCGTCC	57674
rs373250192	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80323748	GCATGAGCCACCATT[C/T]CTGGCCAATTTCTTT	57674
rs373263037	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80265713	GAGCACCAGCTCTCA[C/T]GCGATTAGCTGAGTT	57674
rs373267411	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286201	CCTGGGGTTGGTGTC[A/G]GACGCAGGCCGGTGT	57674
rs373268438	snp	C/T	0.0618563	0.164627	intron-variant	RNF213	GRCh38.p7	17:80313771	AGGTGGTGGAGGTAC[C/T]GGAGGTGATGGTGGT	57674
rs373274594	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315534	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs373282428	snp	C/T	0.000232153	0.0107714	synonymous-codon	RNF213	GRCh38.p7	17:80332169	GAAGATAGACTTGCT[C/T]AGAGACAGCCACATC	57674
rs373301252	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80277970	GCACAGAGAGGGGCC[C/T]GCGCCTGTCCCTTGG	57674
rs373341808	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80272892	AATGTCTACAGTAGG[G/T]GAGGAAAGCGTAACA	57674
rs373368338	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355635	GAATGGGGGCTTACA[-/G]GGGGAAGAAGCGGGG	57674
rs373380068	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359504	TCTAGCCTGGGTGGT[A/G]ACAGAGTGAGACTCT	57674
rs373392176	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80308728	TTTTAATGTCTAGTA[-/A]TAAACATCCCTTGCC	57674
rs373395918	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354899	AAGGGCTGCTGTTTT[C/T]AGTCATGAAGTTAAA	57674
rs373399122	snp	C/G	0.000199101	0.00997551	missense	RNF213	GRCh38.p7	17:80343238	CCCTCAGGTGGATGA[C/G]AGCCGAGTCCTGGGC	57674
rs373402742	snp	A/G/T	4.99824e-05	0.00499891	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354616	AGTGGCTCCAATCTG[A/G/T]TGGCAGCATGGGGAC	57674
rs373409901	snp	A/C/T	5.05245e-05	0.00502595	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371868	ATAATATTTCTCTTT[A/C/T]TGCAGCTTTCATGAT	57674
rs373414070	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393615	AGGAGAGCTGTCAGC[A/G]TAGCACCGAATTCAA	57674
rs373414909	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80350594	GGCCAATAACATTAC[A/G]AAAATAGTGGAATGG	57674
rs373421429	snp	C/T	1.64972e-05	0.00287199	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383932	TTCCTGCAGAAGGTA[C/T]GTCTGGCTTACTGTG	57674
rs373421968	in-del	-/TGGCTCACTGCAACCT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390480	GGCTCACTGCAACCT[-/TGGCTCACTGCAACCT]CTGCCTCCCAGGTTC	57674
rs373432516	snp	G/T	3.2956e-05	0.00405918	intron-variant	RNF213	GRCh38.p7	17:80308971	TAACCATTTTCTGGC[G/T]TCTCCTAAATCCTTG	57674
rs373438033	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	RNF213	GRCh38.p7	17:80346090	GGACTTTGGACAACT[A/G]AGTGACGTTGCTGAA	57674
rs373444242	snp	C/T	3.45507e-05	0.00415622	stop-gained	RNF213	GRCh38.p7	17:80340128	TGCACGCAGCAGCAC[C/T]GAGAAGACTACCAGC	57674
rs373456428	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365682	TGGAACTTGAGTTCT[G/T]CTGCTGAAGGAAAAG	57674
rs373459379	snp	C/T	0.000230681	0.0107372	intron-variant	RNF213	GRCh38.p7	17:80337757	CCCTCGGCGCAGCTG[C/T]GGCCCTTCTGCAGGC	57674
rs373475992	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377231	GGAATATGCCATTTT[G/T]GGAGAAGGGAGGGAC	57674
rs373476884	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388410	TCATGTAATTGGCTG[G/T]GAGGACTCCGCTGGA	57674
rs373484744	snp	C/T	0.000114097	0.00755217	missense	RNF213	GRCh38.p7	17:80336272	TGCAGGGCTACGCAT[C/T]CCTGCTATTTAAGCT	57674
rs373491433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311737	CAGCTGCCTCGAGGC[A/G]TGGGCCTCTCGGTGC	57674
rs373498185	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80270862	ATTTCTCTGATCCTG[A/G]CAGCTCTGCCCTTCT	57674
rs373499847	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80344895	CGTTTCAGTATCAAG[A/G]AGGCTCTGTCGAAGG	57674
rs373504283	snp	C/G	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80290529	CATGGCAGGTGGACA[C/G]ATCTCACGGGAATCA	57674
rs373512045	snp	A/G	6.76007e-05	0.00581341	missense	RNF213	GRCh38.p7	17:80346979	AAAAAGGTCGGCTTC[A/G]TGGGCATCTCCAACT	57674
rs373516280	snp	A/G	3.663e-05	0.00427945	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353552	CGGCCATGAGGAGGC[A/G]ATGGAGACGGAGGCC	57674
rs373527879	snp	C/T	4.94319e-05	0.00497127	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368066	CAGGGCCTGGTTTGC[C/T]TCAGAGCAGATGATA	57674
rs373535520	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381535	GAACACTCTGTTCCG[C/T]TGCCCCCACAGGCTC	57674
rs373537100	snp	A/G	1.65531e-05	0.00287686	synonymous-codon	RNF213	GRCh38.p7	17:80298495	ACTCTCCTTCTCACC[A/G]TTCCGGGAACAAATG	57674
rs373551760	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RNF213	GRCh38.p7	17:80344950	TTTCCTGTTTCACTG[C/T]GGGGTAATAAACCCA	57674
rs373555916	snp	C/T	8.23649e-05	0.00641683	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367924	TCTTCTGGCCAGTTT[C/T]TCTGCTTCAGAACTG	57674
rs373568102	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80322831	CTCCCATTCTATGTG[G/T]TGTTTTTTCACATTC	57674
rs373580367	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270903	CTTTGTCTGCAGGTG[A/G]AGGAGAACAGACAGT	57674
rs373595025	snp	G/T	3.30169e-05	0.00406293	synonymous-codon	RNF213	GRCh38.p7	17:80313071	AACAGTCTTCCAAGG[G/T]ACCCTTGCTGCTACG	57674
rs373602881	snp	C/G	1.64846e-05	0.0028709	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358453	CACGATGCTTCTGAA[C/G]ATTCCTCTTGTGATG	57674
rs373608445	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80349312	GGGCTAGAGCAGCAG[A/G]CCTCGAGGAACGTTT	57674
rs373615872	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80333609	TGAGGCAGGAGGATC[G/T]CTTGAACCACGGAGG	57674
rs373616954	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377902	CGGCCTTCCAGGAGA[A/G]CACAGGCTCACCGAG	57674
rs373627488	snp	C/T	1.65721e-05	0.0028785	intron-variant	RNF213	GRCh38.p7	17:80348311	TTTCTGCACTTGTAC[C/T]CTATCCCCTGTCACC	57674
rs373630555	snp	C/T	8.34913e-05	0.00646055	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386241	TAAGCATAACCCTGT[C/T]GTTTAAAGGTGAGAT	57674
rs373631128	snp	A/G	1.64985e-05	0.0028721	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364536	CTGGTGACCGAGCAC[A/G]TCTTCTTACTAGACA	57674
rs373638772	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80278037	CGCTGGTTGCTGACT[A/G]ACAGGGTGTCCTTTG	57674
rs373643553	snp	C/T	0.000148245	0.00860815	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377772	CACAGCTTGTCCCAA[C/T]GGCCATCCTTGCTCC	57674
rs373647755	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391180	CTAAAGGCCAAAATG[A/G]TATCTCATTTTCAGT	57674
rs373648166	snp	C/T	4.94287e-05	0.00497111	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379669	ACTGCCATGCGCCGA[C/T]TGGAGGCATTGACCA	57674
rs373676083	snp	C/T	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389864	AAACACACCATTGCC[C/T]TCTGGCAGTTCCTGT	57674
rs373676981	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80262328	GATGCAAATTGTCCC[A/G]TACACCTATTGGGAA	57674
rs373686262	in-del	-/TGAAGGTGA			intron-variant	RNF213	GRCh38.p7	17:80313867	AGGTGATGGTGGTGG[-/TGAAGGTGA]TGGTGGAGGTACTGG	57674
rs373703631	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395994	CCTCACTCCCACTCA[C/T]ACCCGCCTCCCTGGA	57674
rs373704192	snp	A/G	3.36022e-05	0.00409877	synonymous-codon	RNF213	GRCh38.p7	17:80347158	CAAAGCCTACGAAAC[A/G]GTGTGTAAGCGCCAG	57674
rs373706530	snp	A/G	0.00013596	0.00824387	intron-variant	RNF213	GRCh38.p7	17:80273432	CCTCGGCTCCCCTCC[A/G]CCCCCGCTCACTCTG	57674
rs373708097	snp	C/T	0.000117622	0.00766794	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388569	TGCTGGAAATGTCCA[C/T]GATGGATTTAATTTT	57674
rs373714785	snp	A/C/T	8.24219e-05	0.00641905	missense, synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361750	ACTGCCCAAGAAGTT[A/C/T]GTGGACATCTTTCAG	57674
rs373736060	snp	A/C	1.68451e-05	0.00290211	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363099	AGCTTTTTTGAATCC[A/C]AGTTTCTGCAGATGG	57674
rs373741594	snp	A/G	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376272	AATATTCTTTGATAC[A/G]TCTTAATGTTAAGTT	57674
rs373749246	snp	A/G	4.94523e-05	0.00497229	missense	RNF213	GRCh38.p7	17:80289698	GAGATGGCTGCTGCT[A/G]AAGAAAAAGTCGGTA	57674
rs373756460	snp	A/T	0.000457804	0.0151226	missense	RNF213	GRCh38.p7	17:80317216	TGGTGGAAATCCAAT[A/T]CCCCGCGGAGCATGG	57674
rs373756919	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80307507	AGCTGGGATTACAGG[C/T]GCACCCCACCACGCC	57674
rs373760480	snp	C/G	0.000131889	0.00811956	intron-variant	RNF213	GRCh38.p7	17:80319174	CTCTGAAACCACCCC[C/G]CTTTGATTTTTGCAG	57674
rs373764161	snp	C/T	4.94645e-05	0.00497291	missense	RNF213	GRCh38.p7	17:80347514	TGCAGCAGACATTCT[C/T]CGAGGGGGACCAGCA	57674
rs373773077	in-del	-/CT			intron-variant	RNF213	GRCh38.p7	17:80269600	ATCCGTCCATCCTAT[-/CT]GTTTATCTATCATCT	57674
rs373778920	snp	A/G			missense	RNF213	GRCh38.p7	17:80340003	TGGCACTGTTGCTGC[A/G]CCGCTGCCTGACCCT	57674
rs373785138	snp	A/G	0	0	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372718	AGATTTCCTCTCGGA[A/G]CCTGAGGGAGGCCCA	57674
rs373797927	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314061	GAGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs373816230	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337266	TGATGGCGTCTGGTA[A/G]AGAGGCAGGCGGGCG	57674
rs373817825	snp	A/C/T	0.000285172	0.0119377	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389391	CACACCGAAAAGGAA[A/C/T]TCAGCACAGCCCCTC	57674
rs373828381	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319794	CCCCCTGTCTCCCAG[A/G]AACAGTCTCGCAGGC	57674
rs373830000	in-del	-/GAGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359610	AGAGCGAGAGAAAGA[-/GAGA]AAGAAAGTAAAGAAA	57674
rs373841238	snp	C/T	0.00953873	0.0683987	intron-variant	RNF213	GRCh38.p7	17:80277423	ACCAACATGGGGAAA[C/T]CCCGTCTCTACTAAA	57674
rs373877122	snp	A/G	4.94189e-05	0.00497062	missense	RNF213	GRCh38.p7	17:80294836	GGGAAGCAGATTGCC[A/G]CTGCGCTCATGCTGG	57674
rs373887772	snp	A/G	9.93065e-05	0.00704581	synonymous-codon	RNF213	GRCh38.p7	17:80346471	CGCCAGGTTCTTTCC[A/G]AAACCGTATGACGAC	57674
rs373888168	snp	A/G	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80348142	CGATGCCGTGGTCCG[A/G]CTGAGCGCCTACTCG	57674
rs373888598	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295429	CAGCTCCTCCTGTGG[C/T]TCTCACAGGTGTGGT	57674
rs373900457	snp	A/C	1.65111e-05	0.0028732	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358291	TCTGTGCTGCAGGCA[A/C]ACCCTCTGGAAGCGG	57674
rs373923748	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281613	ACACAGCCAACTCAC[A/C]CCACTCACACACACC	57674
rs373924505	snp	A/G	3.29484e-05	0.00405871	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389198	CCAGCTCGGTCATTA[A/G]TGCCATCAGTGGACA	57674
rs373927810	snp	C/T	0.000132127	0.00812686	synonymous-codon	RNF213	GRCh38.p7	17:80348118	GATCCTGCTGAACTG[C/T]GCTACGCCCGATGCC	57674
rs373930748	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80273423	AGTGCACTGCCTCGG[C/T]TCCCCTCCGCCCCCG	57674
rs373931475	snp	A/G	1.64751e-05	0.00287007	intron-variant	RNF213	GRCh38.p7	17:80309175	CTATCTCTGGTGGTA[A/G]GTGGAGTCAACACAC	57674
rs373932677	snp	G/T	6.59652e-05	0.00574267	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364390	CCCTTGGGTTCCTTG[G/T]TGGGAGCCGAGTGAG	57674
rs373935348	snp	C/T	1.69461e-05	0.0029108	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288223	GAGGGGACCGGTCCC[C/T]CCACCTCTGCTGGTG	57674
rs373962910	snp	A/G	0.00116891	0.0241472	synonymous-codon	RNF213	GRCh38.p7	17:80345205	GGAAGAAGATCTAGC[A/G]CCCTTCTCCCTCCGG	57674
rs373974094	snp	C/T	0.000263279	0.0114704	intron-variant	RNF213	GRCh38.p7	17:80317151	GCCGTGGCATTTAGT[C/T]GTGAGAGTGGGTGTG	57674
rs374007713	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310284	TGAGATGGAGTTTTG[C/T]TCTTGTTGCCCAGGC	57674
rs374011219	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80336796	GTAATCCCAGCTACT[C/T]TGGAGGCTGAGACAG	57674
rs374022486	snp	A/C	0.000430906	0.014672	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361709	TAGACGCACTCCAGG[A/C]CGCTCCTTGGTTTCC	57674
rs374028228	snp	C/G	0.000832771	0.0203885	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374624	TCTCTCTGATACCAG[C/G]TGGCATCCCTTGGAG	57674
rs374031179	snp	A/G	1.72356e-05	0.00293556	missense	RNF213	GRCh38.p7	17:80340315	CCGTGTTCAATGACC[A/G]GCTGTGTGTTGGGAT	57674
rs374033590	snp	A/G			missense	RNF213	GRCh38.p7	17:80346473	CCAGGTTCTTTCCGA[A/G]ACCGTATGACGACAG	57674
rs374058418	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80309987	TCTCGATCTCATGAC[C/T]TCATGATCCGCCTGC	57674
rs374064401	snp	C/T	6.59859e-05	0.00574357	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386704	GCTATTCCGTGGATG[C/T]CGCCGAGGTCACTGA	57674
rs374068975	snp	A/G	8.34383e-05	0.0064585	missense	RNF213	GRCh38.p7	17:80347318	AAGGATGACATCCAA[A/G]CTTTGGACATCTTTC	57674
rs374072954	snp	A/T	0.000936658	0.0216206	intron-variant	RNF213	GRCh38.p7	17:80295540	GTTCATGCATCTTCC[A/T]CTTCTCCCACCATCA	57674
rs374075886	snp	A/C/T	0.000313046	0.0125071	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361872	CCATGCGTGTGTCAA[A/C/T]GGAGGAGGAATTAAA	57674
rs374125652	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341694	GGTGAGCTGCAAATA[C/T]GACACTGCACTCCAG	57674
rs374131565	snp	C/T	0.000839762	0.0204738	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389937	GTCTGGTCTCTTCCT[C/T]TCTGCTGGACAGAGG	57674
rs374135813	snp	A/C	3.33189e-05	0.00408146	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388598	TTAAAAAACTTTTTT[A/C]TTTCCCAATTTAGGG	57674
rs374142793	snp	A/C/G			intron-variant	RNF213	GRCh38.p7	17:80342556	TCTCTCTCTCTCTCT[A/C/G]TTTTTATATATATAC	57674
rs374178105	snp	C/T	0.000212811	0.0103131	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288054	CCTCTCCGCGCCCAC[C/T]GAGGTTGGCGACAGC	57674
rs374178902	snp	A/G	3.3248e-05	0.00407712	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354105	GAACGAGAGCTGCAC[A/G]CGCAATATGCGGAGG	57674
rs374217820	snp	A/G	7.82595e-05	0.00625489	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287832	CAAAAAGAAGAAAAG[A/G]AAGAAGAAAAAGAAG	57674
rs374236787	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80322812	ATATGATTGCAAGTA[A/T]TTTCTCCCATTCTAT	57674
rs374242029	snp	C/T	0.000459649	0.015153	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363586	GGCACCGCTCAGCCA[C/T]GCCCTGCTGTCCGTC	57674
rs374248262	snp	C/T	3.29478e-05	0.00405867	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376290	TTAATGTTAAGTTTT[C/T]TTCCTGTCAGCAATG	57674
rs374248369	snp	C/T	6.59859e-05	0.00574357	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388714	ATAAACCTGATCCTG[C/T]GCACGGGGCTTTCTG	57674
rs374254445	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326174	CGCAAGTTAGCATGT[A/G]GTAGAGTGATGCCAT	57674
rs374262786	snp	A/G	1.67458e-05	0.00289355	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373090	CAGCCAGCGGGGGAT[A/G]GAGTTCGTGCAGGGC	57674
rs374282644	snp	G/T	0.000155988	0.00883005	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288349	GAGCAACAGGCAGGG[G/T]CCTCAGCCTCTATGG	57674
rs374285445	snp	A/G	0.000437904	0.0147905	intron-variant	RNF213	GRCh38.p7	17:80317134	TCCTTTCATGGGAGT[A/G]TGCCGTGGCATTTAG	57674
rs374285482	snp	C/T	6.61627e-05	0.00575126	synonymous-codon	RNF213	GRCh38.p7	17:80343220	AACAATTCGACTGAT[C/T]GACCCTCAGGTGGAT	57674
rs374288665	snp	A/G	0.000166909	0.00913381	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367720	GCCCTCCCCCCTGCT[A/G]ATGACTCCTGTCCCT	57674
rs374322197	snp	C/T	0.000312935	0.0125048	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389965	AGGGACTGCGCTCCC[C/T]TCTCCCTGCAGGCTT	57674
rs374353186	snp	C/T	0.000233318	0.0107984	intron-variant	RNF213	GRCh38.p7	17:80338043	CTGGTGGTGTCATCT[C/T]GTCCGTGAGGGCTGT	57674
rs374358484	in-del	-/AG			intron-variant	RNF213	GRCh38.p7	17:80301458	CTCAAACAAGTGAAC[-/AG]AAAAACTCAGATCTA	57674
rs374364100	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307850	CCACCATGCCTGGCC[A/G]TCTGTTTTTTTTTTT	57674
rs374369695	snp	C/T	0.000153988	0.00877328	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353998	GGCAGAAACGGATGA[C/T]CCAACCGTCTCCACC	57674
rs374372357	in-del	-/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352460	GGGAGGGAGAGTGGC[-/G]GGGGGTCGGACTATC	57674
rs374376661	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294019	CTGAGGAGGCCTGTC[C/T]GGGCGCTTCCCATTT	57674
rs374380704	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360620	TCAGAAGGCACGAGC[A/G]CCTGGAGCATCCCCT	57674
rs374393563	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80292410	AGAGAAAACGAAGCC[A/G]GAAGAAGGGCTGCGG	57674
rs374413466	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383452	CAGCCAGAATGTTAG[G/T]AAGAGAAATATAGGT	57674
rs374437352	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80290453	TGCATGTGTGTGTGC[-/G]AGTGCATGTGTGTGT	57674
rs374446674	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363850	TCACCAGGAGCCTGC[C/G]AAGTGCCAGGCATGT	57674
rs374448364	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393273	CACGTGAGCCACACA[-/G]TGCTGGGCTTACACA	57674
rs374458508	snp	C/T	0.000229384	0.010707	synonymous-codon	RNF213	GRCh38.p7	17:80339623	GTGTGGGAGTGAGGC[C/T]GCCAGGTACCGCATG	57674
rs374468136	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384890	GGAAGAACTTTTCCC[A/G]TTTTCAAGCTCCACG	57674
rs374498737	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382056	GTCTTCAGTTCCGAA[A/G]TCAGCCCCGTAGGTC	57674
rs374516436	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365244	GCAGCGCTGGCTGTC[C/T]GACCTTTGGAGCACA	57674
rs374519930	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353150	ATGGCACTAGGAGCA[A/G]GGCCACCGTGTTTCG	57674
rs374527954	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80317174	TGGGTGTGACCTGTG[C/T]GCGGGTTTTGCAGGT	57674
rs374557376	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281562	ACACCCCCCAAGACA[A/C]ACGCCCCACTCACAC	57674
rs374558834	snp	C/T	0.000394028	0.0140306	intron-variant	RNF213	GRCh38.p7	17:80273449	CCCCGCTCACTCTGC[C/T]CAGGAAAATCTCACT	57674
rs374596330	snp	A/G	0.000437904	0.0147905	missense	RNF213	GRCh38.p7	17:80334127	ACTTCGACGACTTTC[A/G]CCGTGAAACACTGGA	57674
rs374627135	snp	C/T	3.295e-05	0.00405881	synonymous-codon	RNF213	GRCh38.p7	17:80307181	AATGCTGTTGCGACT[C/T]CTGGACACTTACCGG	57674
rs374629814	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268164	TGTTCCATTATGTAT[A/G]TGTACCACATTTTCT	57674
rs374631434	snp	G/T	0.49423	0.0534032	intron-variant	RNF213	GRCh38.p7	17:80307862	GCCGTCTGTTTTTTT[G/T]TTTTTTTTTTTTTTA	57674
rs374682633	snp	G/T	3.30415e-05	0.00406444	intron-variant	RNF213	GRCh38.p7	17:80290737	ACACCAGGTGAGCGT[G/T]TCTGTAGGCTTGGGA	57674
rs374686009	snp	C/T	3.34375e-05	0.00408872	missense	RNF213	GRCh38.p7	17:80346649	GAGACTTGGAGCTGC[C/T]GGGCTTCCCCACCAG	57674
rs374689837	snp	A/G	3.30786e-05	0.00406672	synonymous-codon	RNF213	GRCh38.p7	17:80347368	CAAGTGCTCAGAGGA[A/G]GTCAGCCCCATGCAG	57674
rs374694492	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80315769	GTGACAGTGGTGATG[C/G]TGGTGGTGGTGGTGG	57674
rs374712696	snp	A/G	2.45709e-05	0.00350498	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386896	TGAGCCTCAAGGTAG[A/G]GCTGACTCCTGCCAC	57674
rs374717242	snp	A/C/G	0.000230823	0.0107406	intron-variant	RNF213	GRCh38.p7	17:80306218	CACTGATCTCACTGC[A/C/G]TCTCTTTTCTCCGTC	57674
rs374751421	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315234	GTGGTGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs374752661	snp	C/T	8.25198e-05	0.00642286	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375880	CCAGAGGTGAGTAAC[C/T]GCCTGCAGGGCTGTG	57674
rs374772595	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267906	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	57674
rs374792078	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315378	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs374801924	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305576	GAATTCTTATTCCGT[A/G]TTCTGAATTCTATAT	57674
rs374808184	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290376	GTGCGTGTGTGAGTG[C/T]GTGCACGTGTGTGCG	57674
rs374810044	snp	A/G	4.73552e-05	0.00486573	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363833	CTTCATCTGGCGCGC[A/G]CTCACCAGGAGCCTG	57674
rs374817637	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329340	TCTAGAATTACAGAC[C/T]GGAAGTCATTTTCCT	57674
rs374824795	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387822	ACCTCATGCACTGAA[A/G]CCACACAGCAGGCAC	57674
rs374836352	snp	C/T	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321362	GGAATGCTCAACCTA[C/T]ATTTCATTTTTTTCC	57674
rs374838781	snp	A/C/G	3.32985e-05	0.00408024	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319529	CCTGCTGCTCGCACC[A/C/G]TCCTGCATGTGTTCC	57674
rs374853942	snp	C/T	3.30775e-05	0.00406665	intron-variant	RNF213	GRCh38.p7	17:80290748	GCGTGTCTGTAGGCT[C/T]GGGAGGAATCCCTCA	57674
rs374855138	in-del	-/G	0.000565894	0.0168115	intron-variant	RNF213	GRCh38.p7	17:80289609	AAAAAAAAAAAAAAA[-/G]AAAATGTGGAGGCCG	57674
rs374859856	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80300359	AGCCTCTGCCTCCTC[A/G]GCACAAGCGATTCTG	57674
rs374866812	snp	C/G	0.000153988	0.00877328	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361724	CCGCTCCTTGGTTTC[C/G]TCTCTGCAGGACTGC	57674
rs374873588	snp	A/G/T	0.000120408	0.00775836	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354204	TGCCCCTGCCCCCAC[A/G/T]TGGGCTCTTCCTGAG	57674
rs374900333	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384339	GCGTACGTGGAAGAC[A/G]GGAGTGAGTGGGTGT	57674
rs374918813	snp	C/T	0.000138966	0.00833449	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287879	CCTCAGAGCTGGCTT[C/T]CTTGCCCCTTTCTCC	57674
rs374950734	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	RNF213	GRCh38.p7	17:80345748	GGCTGAAAATGTGGC[C/T]TTCGCCAATAAGGAC	57674
rs374966000	snp	C/G	1.65236e-05	0.00287429	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386309	CTGGACACTGAGTTT[C/G]AGATCCTCTTGCCAC	57674
rs374977881	snp	C/T	0.000132188	0.00812874	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364585	GCCTCAGCACATGCA[C/T]GGATCCACCCTTTTC	57674
rs374982691	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80304137	TTGTTCCTAAAGATC[C/T]AATCGTTCAGGTAAA	57674
rs375006554	snp	A/T	3.29973e-05	0.00406172	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369728	CATCTCGCTTCTGCA[A/T]GTCTCATGCAGTGAG	57674
rs375015335	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80265749	GAAAGCTGAGCTTCC[A/C]GGCATGCAGGGCGTC	57674
rs375030119	snp	C/T	8.27534e-05	0.00643194	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360046	CTCTTCTTATCATCC[C/T]TCACCTTATTGCAGA	57674
rs375033522	snp	C/T	0.000201062	0.0100245	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373174	GCAGCAGGTGAGAAG[C/T]GGGGCCGGGCAGCAC	57674
rs375053532	snp	C/T	0.000132317	0.0081327	synonymous-codon	RNF213	GRCh38.p7	17:80346810	CACCTTCCGGCAGTG[C/T]GCCCGCTTTCAGCAG	57674
rs375059444	snp	C/T	3.29538e-05	0.00405904	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369553	GTGCAACAGTTTCTT[C/T]GTAGACCTGGTGTCC	57674
rs375071973	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377863	TTGGAGGAGGGGGAT[C/T]GTGGGTCAGGAGAGT	57674
rs375082733	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80263209	GCCAGCCCAGTAGCC[C/T]TGGGCTGCCTGCTCA	57674
rs375094054	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326561	CATTCCAGTATCGTG[C/T]AGAATAGTTGCGCTG	57674
rs375097553	snp	C/T	0.00054359	0.0164772	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358422	CAAGAGATCTTTGGA[C/T]GTTTATTTTCAGTGA	57674
rs375101877	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314811	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs375102492	snp	A/G	3.2994e-05	0.00406152	missense	RNF213	GRCh38.p7	17:80347859	AGAAGCACTATCTGG[A/G]TATCAACACGGTGCT	57674
rs375108610	in-del	-/CTTT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371809	CGATAGATAGATGCT[-/CTTT]TTTTTAGTAAGGTAT	57674
rs375117619	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261494	GGGCCGGGCCCTGGG[A/G]GAGTCCAGGGCGGGA	57674
rs375118927	snp	C/T	4.97129e-05	0.00498538	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381018	GCCAAACAATGGGCT[C/T]AGTTAAGAACCTGCT	57674
rs375135053	snp	A/C	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80307234	TGCAGTCTCTCCCTC[A/C]CATGCGGCCCCCGGG	57674
rs375137546	snp	C/T	8.23906e-05	0.00641783	synonymous-codon	RNF213	GRCh38.p7	17:80345994	TATGGAGGAGACGGC[C/T]GACAGGCTGGGCTCC	57674
rs375141596	snp	C/T	6.58913e-05	0.00573945	synonymous-codon	RNF213	GRCh38.p7	17:80346195	CACAGAAGTCCTCTG[C/T]GCCTCTCAGGGTTTC	57674
rs375150871	in-del	-/ATGCCTG			intron-variant	RNF213	GRCh38.p7	17:80333436	AGTGGCTCATGCCTG[-/ATGCCTG]TAATCCCAGCACTTT	57674
rs375180543	snp	C/T	1.72077e-05	0.00293318	intron-variant	RNF213	GRCh38.p7	17:80350400	TGCCTCAGCTAAGTA[C/T]GTTTTTAGTATTTTT	57674
rs375197868	in-del	-/TGGAGGTAC			intron-variant	RNF213	GRCh38.p7	17:80315007	TGGTGAAGGTGATGG[-/TGGAGGTAC]TGGAGGTGATGGTGG	57674
rs375203066	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361618	GGTACCCCTTTGTCT[A/G]CGAGCTCCCATTCAA	57674
rs375208924	snp	A/G	2.23686e-05	0.00334422	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360227	GCTACCTCAAGACAG[A/G]TCAGATTCAGCACAG	57674
rs375218104	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392821	TCTCGAACTCCTGAC[G/T]TCAAGTGATCCACCT	57674
rs375218846	snp	G/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386433	AGGAAAACAACAGGT[G/T]TGTGCACGAGCCACC	57674
rs375219887	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330331	TGTTTGTCTGTGTTT[A/G]TTAAGAGAAAGCCCT	57674
rs375222004	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307693	TAGCTGGGATTACAG[A/G]CGCATGCCACCACGC	57674
rs375230241	snp	A/G			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360187	GTGGGTCCAGGCTCA[A/G]TACATCACAGACGCA	57674
rs375239709	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382012	TCGGGAGCGTCTGCA[C/T]GCAAGTGTTCAGTGT	57674
rs375246029	snp	C/G/T	6.59678e-05	0.00574284	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380839	TTTCCAGAGACAAGG[C/G/T]AGACAGAACGCAGAC	57674
rs375274212	snp	C/G	4.96208e-05	0.00498076	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383965	TCCCTCCCTCTTTCG[C/G]TGCAGAGTTCCCCAG	57674
rs375296966	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314580	GTGGTGGTGGTGGTG[A/G]TGGTGGAGGTAATGG	57674
rs375300904	snp	A/G	1.65671e-05	0.00287807	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371989	AACTGCCTGGAGGTA[A/G]GTGAACTCTCTCTTC	57674
rs375328644	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286330	TACACTGAGCATGGG[C/T]TTCCTCTGAATTTAA	57674
rs375335327	snp	C/T	3.30628e-05	0.00406575	intron-variant	RNF213	GRCh38.p7	17:80349920	CGGTGAGGTTCCCTG[C/T]CTTCCCTGCTGCCCT	57674
rs375351035	snp	C/G	0.000151325	0.00869711	intron-variant	RNF213	GRCh38.p7	17:80263808	TGCTGGTGGAGGCTG[C/G]GGCAGTGGGGACCCC	57674
rs375373386	snp	A/C/G	1.66172e-05	0.00288242	intron-variant	RNF213	GRCh38.p7	17:80295831	ATTATTATTTTTTGT[A/C/G]AAAATGTTTTTTATA	57674
rs375383189	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388466	AGATGGTGGGTTAAT[A/G]ACGGAGAGGGGCGCT	57674
rs375385075	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80314644	TACTGGAGGTGATGG[C/T]GGTCGTGGAGGTGAT	57674
rs375388239	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314502	GAGGTGATGGTGGTG[A/G]TGGTGGAGGTAATGG	57674
rs375394552	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366187	CGGGCAGGAAGTTGT[C/T]GACGGAACTGCTGCA	57674
rs375400927	snp	C/T	0.000181185	0.00951628	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377716	TTTCAATGTGGGTCA[C/T]TGGGTGAAACCTCAT	57674
rs375408364	snp	C/T			missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288004	CAGCCGAGCCAGCCC[C/T]CAGGCACAGCCACCA	57674
rs375413426	in-del	-/TT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80342744	TATATTATATATATA[-/TT]GTATGTATATATATA	57674
rs375417663	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269420	ATCTATCCATCCATC[C/T]ATCCATTCATCTATT	57674
rs375439063	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320429	GCGATCCTGGCTCAC[C/T]GCAACCGCTGCCTCC	57674
rs375448539	snp	A/C/G			intron-variant	RNF213	GRCh38.p7	17:80315489	GAGGTAATGGAGGTG[A/C/G]TGGTGGTGGTGGTGG	57674
rs375458667	snp	C/G	0.000153988	0.00877328	intron-variant, missense	RNF213	GRCh38.p7	17:80319371	TGTGTTCTGCCATGA[C/G]CCAGCTAAGGGCTAT	57674
rs375460513	snp	C/G	1.7192e-05	0.00293185	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385487	TAGGGTGGTTTGGCC[C/G]TTTCAGGGGGTTGCT	57674
rs375489367	snp	G/T	0.000437904	0.0147905	intron-variant	RNF213	GRCh38.p7	17:80337575	CGTGTTCTCTCCTTT[G/T]GTCCCCATAGTGTGA	57674
rs375490430	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367624	GGATCACAAAGGCCT[C/T]GCACCCCACACCCCA	57674
rs375499861	snp	A/G	6.58892e-05	0.00573936	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383839	ATTTGGAGCTGCAGG[A/G]AAAGAATTACAGTTG	57674
rs375507267	snp	A/G	1.65111e-05	0.0028732	missense	RNF213	GRCh38.p7	17:80345497	ATCCCCCAGGCCACC[A/G]ACCCCGACAAAACGT	57674
rs375519369	in-del	-/ATCT	0.0146334	0.0842766	intron-variant	RNF213	GRCh38.p7	17:80269658	TCTATTCATCCATCA[-/ATCT]ATCCATCCATCCATT	57674
rs375529318	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80277424	CCAACATGGGGAAAC[C/G]CCGTCTCTACTAAAA	57674
rs375541080	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392020	TGATCTGCCCGTCTC[A/G]GCCTCCCAAAGTGCT	57674
rs375548876	snp	A/G	4.94189e-05	0.00497062	missense	RNF213	GRCh38.p7	17:80346175	GAAAACGGGACTCGC[A/G]TGATCACAGAAGTCC	57674
rs375554114	snp	C/T	6.59685e-05	0.00574281	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80288804	GCCCTCTCCTGCCCA[C/T]GGCTGCGCCTCTTTC	57674
rs375561682	snp	G/T			stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383014	GAATTGTCAACTAAA[G/T]AAATGAGGAACAACT	57674
rs375563057	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376118	CAAAATTAATGCTTA[C/T]GTATGTGGATGCTGT	57674
rs375566084	snp	C/G/T	3.29491e-05	0.00405877	missense	RNF213	GRCh38.p7	17:80306400	GGTCGTTTTCCTGCT[C/G/T]ATATCCTGGACTGTC	57674
rs375577940	in-del	-/AAAG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359617	GAGAAAGAGAGAAAG[-/AAAG]TAAAGAAAGAAAGAG	57674
rs375580063	snp	A/G	0.0103295	0.0711199	intron-variant	RNF213	GRCh38.p7	17:80296395	TTAGGAGGTTGTGGC[A/G]TGACGCCAGCCTGAA	57674
rs375587766	snp	C/T	4.94197e-05	0.00497066	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367975	GGTTTGGGATTCAGC[C/T]GTGCTCCATCTGCCT	57674
rs375593774	snp	C/T			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393399	AAGTGAAATTCTTCC[C/T]GAAATGGCATCTCAG	57674
rs375602932	snp	C/T	0.000775455	0.0196755	synonymous-codon	RNF213	GRCh38.p7	17:80346954	CATTGAAGACGATCC[C/T]GCCCCCCACAAAAAG	57674
rs375603416	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355849	GGGTGAACGGGAATG[A/G]GGACTTACAGACACC	57674
rs375638904	snp	A/G	0.00136777	0.0261154	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393498	TCGAGAAATGAGATA[A/G]AATTATTTCCTCAGC	57674
rs375651581	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80262409	ATTGGGACAGGGGCT[C/T]GGGGCTGGAGAGGGG	57674
rs375652015	snp	C/T	0.000856249	0.0206734	missense	RNF213	GRCh38.p7	17:80345054	GCAATCCGAGTTTTA[C/T]TGGCGACACACTGAG	57674
rs375652626	snp	A/G	0.000148656	0.00862008	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386811	GAGGGCAGAGAGACC[A/G]TGCAGGAGTTCGATC	57674
rs375665425	snp	C/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80343963	GCCATTTGTATATCG[C/T]TGAAATCCTGGAAAG	57674
rs375665467	snp	C/T	6.68192e-05	0.00577972	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373039	TATCCGGGTGGAGAA[C/T]GACTGGCACCGGGTG	57674
rs375665654	snp	C/T	1.64768e-05	0.00287021	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381544	GTTCCGTTGCCCCCA[C/T]AGGCTCTGATAAACA	57674
rs375669918	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367028	TTGAATACAGGACTG[C/T]CAGGAATTGCAAAAA	57674
rs375676516	snp	C/T	1.64966e-05	0.00287194	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361905	TAGATGTTTAGATAC[C/T]GGCTAAGGGTCAGGT	57674
rs375680172	snp	C/G/T	1.64765e-05	0.00287019	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353674	GCAGTGATGTAAGTT[C/G/T]TGGTTCTTGGGACCT	57674
rs375686007	snp	A/G	1.64988e-05	0.00287213	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368127	GAATTCTCTCCAGCT[A/G]TTTCCCAAGCGCACA	57674
rs375688032	snp	C/G/T	4.98818e-05	0.00499388	missense	RNF213	GRCh38.p7	17:80346514	CTGGATGAAATAACA[C/G/T]GGGCACAGGATCTTT	57674
rs375693737	snp	C/T	4.9764e-05	0.00498794	missense	RNF213	GRCh38.p7	17:80295621	CGGACGGAAAAAGCA[C/T]GGACTTTTTGCCTGT	57674
rs375697820	snp	C/T	9.88533e-05	0.00702971	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358363	ATTCATCGACAGAGA[C/T]GGCAACCTAGAGTTA	57674
rs375704542	in-del	-/AACGTGG			intron-variant	RNF213	GRCh38.p7	17:80284712	CTGCCTTCCGGACGG[-/AACGTGG]CTCCCCCACTGAGCC	57674
rs375733337	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367335	TAAAAAATGATCTAT[C/T]GCAGCAGCTTGGGAG	57674
rs375753576	snp	A/C/G	1.64787e-05	0.00287038	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379698	CACAAACCTCGGGAC[A/C/G]GCTTTCATCTGGTCA	57674
rs375768276	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314535	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs375771412	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80349844	CACAGGCAGGGCTCC[A/G]AAACCCACACTCCTG	57674
rs375774205	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80342381	GGTGACCAGGAGAGT[A/G]AGTAGGTAACGGCTG	57674
rs375776199	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80314013	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs375776649	snp	C/G/T	3.30002e-05	0.00406192	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364542	ACCGAGCACGTCTTC[C/G/T]TACTAGACAAGGTGA	57674
rs375777559	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385419	AACAGCACCTCAGAC[A/G]TGCTTGTGACTGCAC	57674
rs375783747	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80347053	ACGTGGCAGCCCCAA[C/T]GAGACAGAGCTCATA	57674
rs375786574	snp	A/G	3.29473e-05	0.00405864	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389868	ACACCATTGCCCTCT[A/G]GCAGTTCCTGTCTGC	57674
rs375796011	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80312681	GCCCCTCTCTGGGGC[A/G]TGCTTTTCCCCCTCA	57674
rs375796552	in-del	-/TCCCGGCGATGCC			intron-variant	RNF213	GRCh38.p7	17:80278230	TCTTGCTGTGAGGTC[-/TCCCGGCGATGCC]CGGTGTGGTGTGGAA	57674
rs375798834	snp	A/C/G	4.9442e-05	0.00497182	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374500	ATGGATAGGTACCTG[A/C/G]TGTACGGCGATGAAT	57674
rs375801026	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378540	AGCTCACTATAAACA[C/T]TGAACTCCTGGGCTC	57674
rs375813322	snp	C/T	6.59783e-05	0.00574324	missense	RNF213	GRCh38.p7	17:80289663	CCTTGTTCCAGGAAG[C/T]TGAGACCAAGACCAA	57674
rs375819620	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281676	ACACACCCCAACATA[C/T]GCAAGTCCCACTCAC	57674
rs375826676	snp	A/C	1.66729e-05	0.00288724	synonymous-codon	RNF213	GRCh38.p7	17:80346753	GGTCCACCTGGTGTC[A/C]TTCCAGTGCAGCCCG	57674
rs375845942	in-del	G/TT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392606	CTCAGGATTTCTGGG[G/TT]TTTTTTTTTTCTCGC	57674
rs375867481	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354435	TCTGTTTCTGCCTTT[A/G]TACAGCCTCTTTCTT	57674
rs375895553	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80290459	TGTGTGTGCGAGTGC[A/G]TGTGTGTGTGCACGT	57674
rs375919891	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80292123	TGAGACAGAGTCTGT[C/T]GCTCAGGCTGGAGTA	57674
rs375935660	in-del	-/GTCC			intron-variant	RNF213	GRCh38.p7	17:80269764	CTTATCTATCCATCC[-/GTCC]ATCCATCCATGTATC	57674
rs375961747	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362546	GCAAAGCTGATTTTT[-/A]AAAAACAACAGCCGC	57674
rs375963112	snp	C/T	6.80828e-05	0.0058341	intron-variant	RNF213	GRCh38.p7	17:80343108	CCACCACTCCCAGCC[C/T]TAATTTCTGTATTAA	57674
rs375967982	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384363	TGGGTGTGTGCCGGC[A/G]GTGCTGGGGTACTGG	57674
rs375980334	snp	A/C	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80347940	AGTTCATCAATGTCA[A/C]AGCACATCATTTCCA	57674
rs375988826	snp	C/T	9.8934e-05	0.00703258	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381771	GATCACACAGCACAA[C/T]GGCAGCGCAAGCAGG	57674
rs375998023	snp	A/T	3.29484e-05	0.00405871	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376451	GGAACGGTGACAGAA[A/T]TGGCCATTCATGCTG	57674
rs376008735	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340419	CGGGGCCCTTCCCCC[C/G]TCCAGCAGATGAAGC	57674
rs376053120	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80297632	CTCTACAAAAAATAC[A/G]AAAAACTAGCCAGGC	57674
rs376060852	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370985	ACATTTTGGGGCAAT[C/T]TGTGGTGATATTAAT	57674
rs376063933	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80350668	AATTAGCCTTCCACA[A/G]TGCACCTCTAGTCCC	57674
rs376078964	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80274208	AAATGTGCTGGCTGG[C/G]AGGTTACCCTTCTTG	57674
rs376088132	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80336802	CCAGCTACTCTGGAG[A/G]CTGAGACAGAATTGC	57674
rs376093266	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312453	GTCAGGAGCCTGGCT[A/G]TGGTCTGGCATGGAG	57674
rs376100931	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80295948	TGATTTTACCACTCA[C/G]TGTGGTCATGTCAGT	57674
rs376102448	snp	A/C/G	0.00010683	0.00730778	missense	RNF213	GRCh38.p7	17:80340332	CTGTGTGTTGGGATC[A/C/G]TGGCCTCGGAGCGAG	57674
rs376135559	snp	C/G	6.60033e-05	0.00574433	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361913	TAGATACTGGCTAAG[C/G]GTCAGGTGTAGAGCT	57674
rs376147332	snp	A/C	0.0107246	0.0724382	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359758	TGTTACAAGTTATCA[A/C]AGCCAGACAGGTTCA	57674
rs376153598	snp	A/G	5.0767e-05	0.00503795	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386842	TGGAGAAGATTCAGC[A/G]GCAGATCGTCAGCCG	57674
rs376154998	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326051	GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC	57674
rs376157037	snp	A/G	5.02231e-05	0.00501089	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390211	GGTATGGATTTGCAC[A/G]CCTATGGGGCGGGGC	57674
rs376159210	snp	A/C/G	3.35944e-05	0.00409833	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388570	GCTGGAAATGTCCAC[A/C/G]ATGGATTTAATTTTA	57674
rs376159840	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80271409	AGATCTCAGAGGAGG[A/G]GAGGGCAGTGACGAA	57674
rs376174162	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80299725	TTCCCATCCTCCACC[A/C]TCTGATAAGCCCCAG	57674
rs376175150	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351550	TAAAACTCATCGGAA[C/T]GGGTGGCCGTGAGAC	57674
rs376188478	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80315075	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs376193046	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358250	CGCCACTCTGGTTCC[C/T]CTGACCCGTGGTGGC	57674
rs376216253	snp	A/G	3.29636e-05	0.00405964	synonymous-codon	RNF213	GRCh38.p7	17:80346303	CCACGAGCACAGCGC[A/G]ATGCTCTTAGCGCAG	57674
rs376227836	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362376	AATAAGAAAATACCC[C/T]AAGTTTTAAAAAATG	57674
rs376254264	snp	A/T	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80306463	GAGCAAGTCTTGAAT[A/T]CGCAGGTTTGTGTCT	57674
rs376262420	snp	A/G	3.29489e-05	0.00405874	missense	RNF213	GRCh38.p7	17:80344685	CTTTCCAGCGTACAC[A/G]TGTACCCCAGTTCAG	57674
rs376265862	snp	C/T	0.000101143	0.00711064	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373117	GGGCCTCTCCAAGCC[C/T]GGCCGCCCGCACCAG	57674
rs376267168	snp	A/G	3.31307e-05	0.00406992	synonymous-codon	RNF213	GRCh38.p7	17:80298351	GGTGAACCTGTGCCA[A/G]AGATGCATGGACACA	57674
rs376268612	snp	A/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80344923	AGGCACCCCGGAGGA[A/T]TGCCTCCAGCATTTC	57674
rs376272385	snp	A/G	0.00010726	0.00732245	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353495	TGGTAACGCAATCAC[A/G]TTTGCTTCGACTGCA	57674
rs376286234	snp	G/T	0.000307953	0.0124049	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372501	TAATATCCTTTTCTT[G/T]CTTGTTCCTTGTTCC	57674
rs376291993	snp	A/G	8.23798e-05	0.00641741	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369638	CTCTCTCTCCTCTTC[A/G]TCCAAAAGGGGCGCT	57674
rs376321329	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310060	GCCCAGCCTCCCATG[A/G]ATCAGTTTTACCTGT	57674
rs376331420	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80281540	ATGCCCCACTCATAC[C/G]ACTCACACACCCCCC	57674
rs376336113	snp	C/T	0.0142736	0.0832652	intron-variant	RNF213	GRCh38.p7	17:80306838	GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA	57674
rs376340562	snp	C/T	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80345579	TCCGGTGTGGGATCC[C/T]GGTTATCATCATGGG	57674
rs376343207	snp	C/T	0.000131783	0.00811628	missense	RNF213	GRCh38.p7	17:80294840	AGCAGATTGCCGCTG[C/T]GCTCATGCTGGACAG	57674
rs376344002	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354002	GAAACGGATGACCCA[A/G]CCGTCTCCACCAACA	57674
rs376347002	snp	A/T	3.29473e-05	0.00405864	missense	RNF213	GRCh38.p7	17:80291628	CCTGTTCATTCACAG[A/T]GACTTGGGTCATGAC	57674
rs376349527	snp	A/G	1.76368e-05	0.00296953	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383112	TTGCTCCTCGGTCCA[A/G]AAAGGAAGGGTCCCG	57674
rs376351745	snp	C/T	6.76922e-05	0.00581735	missense	RNF213	GRCh38.p7	17:80343276	TGCCCTTCCTGGATG[C/T]GCAGTATCAGAAGGT	57674
rs376352220	snp	A/G	0.00023964	0.0109436	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354196	ACCCCTCTTGCCCCT[A/G]CCCCCACGTGGGCTC	57674
rs376391467	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80309829	GGCGTGATCTCGGCT[C/T]ACTGCAAGCTCCGCC	57674
rs376392189	snp	C/T	1.6609e-05	0.0028817	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369865	ACTGCTTTTGAAGTA[C/T]AGGTAAGAACAACAT	57674
rs376399365	snp	A/G	2.02982e-05	0.0031857	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381745	GAGGAAAGGGGCAAG[A/G]GCTGGGCGGGGATCA	57674
rs376425442	in-del	-/CATC			intron-variant	RNF213	GRCh38.p7	17:80269571	TTCTATCTGTCCATC[-/CATC]TATACTATCTATCCG	57674
rs376434046	snp	A/G	1.64863e-05	0.00287104	intron-variant	RNF213	GRCh38.p7	17:80309205	CAAGGTATCACACCC[A/G]GGATAGGTGCGGAAT	57674
rs376439754	snp	C/T	3.30082e-05	0.00406239	missense	RNF213	GRCh38.p7	17:80295699	TTGTAGTGGAAAAAA[C/T]TGAGCTTTTATTAGA	57674
rs376444660	snp	A/G	0.00636936	0.0560724	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371349	GGACAGATTTTCTTC[A/G]TGTTCTCCCATATGC	57674
rs376454444	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80338995	CAAATGATACCATTT[A/C]TCTCTACAATGACTC	57674
rs376455231	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80350749	GGCTGCAGTGAACTG[C/T]GATCCCACCACTGCA	57674
rs376459639	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396739	TTTCCCCCCCACCCC[C/G]CCCCCCCAACCAGAG	57674
rs376485823	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80262966	AGTGTGCCCTGAGGC[G/T]TCTTACTGGGGAGGG	57674
rs376492489	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391776	TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTGAG	57674
rs376499993	snp	A/G	0.000115916	0.00761214	intron-variant	RNF213	GRCh38.p7	17:80344032	TCTGTACTGTGGGGC[A/G]TTTTCGCCTGGCGTG	57674
rs376505157	snp	A/G	1.65168e-05	0.00287369	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390134	AGAGCTGCACGAAAT[A/G]ATAATCTTGAAACTA	57674
rs376512471	snp	C/T	0.000231118	0.0107474	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352912	GGAAAGACACAAAGA[C/T]AGTTGTGGGTGGCTT	57674
rs376516788	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314877	GAGGTAATGGAGGTG[A/G]TGGTGGTGGTGGAGG	57674
rs376523817	snp	G/T	0.000131937	0.00812103	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367759	TCAGTGTCTTCGAGA[G/T]AACTCTGACGTGAAG	57674
rs376541167	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265714	AGCACCAGCTCTCAC[A/G]CGATTAGCTGAGTTA	57674
rs376547997	snp	C/G/T	0.000115381	0.00759467	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381513	CTCTACAAACCAGAT[C/G/T]CCCGCTGAACACTCT	57674
rs376577890	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80317785	GTTATCAGCTCAGTG[G/T]GTCCCTTGCCTTGTT	57674
rs376608771	in-del	-/G	0.00398564	0.0444627	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384171	TTAGCAGTGACCTGT[-/G]GGGGAAGCTGGAGGC	57674
rs376616464	in-del	-/CACTCACAC			intron-variant	RNF213	GRCh38.p7	17:80281203	ATACCCCACTCACAC[-/CACTCACAC]ACACCCCCACACACA	57674
rs376629463	snp	C/T	0.000800412	0.0199891	intron-variant	RNF213	GRCh38.p7	17:80328003	GAGTAAGCATCGAGT[C/T]GATACGCACTTCAGG	57674
rs376630260	snp	A/G	0.00038174	0.0138103	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319510	CTCAGTGTGCTGCAC[A/G]GTCCCTGCTGCTCGC	57674
rs376634963	in-del	-/CG			intron-variant	RNF213	GRCh38.p7	17:80323836	AGTACTTTTTTTTGG[-/CG]GGGGGGGTGCTATTG	57674
rs376636445	snp	A/G	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389164	CCTCTCCTGCTTTTC[A/G]TTTCCCAGGACTCCC	57674
rs376655959	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80275168	TGTGTGTGGGGTGAG[G/T]GGGATGTGTGTGTAT	57674
rs376676256	in-del	-/GGGTGAGTGGGGTGAGTGTGGGGA			intron-variant	RNF213	GRCh38.p7	17:80274700	GGGTGTCTGGGGGGG[-/GGGTGAGTGGGGTGAGTGTGGGGA]GTGAGTGGGGTGAGT	57674
rs376689767	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377283	ATTCAAAGGCCCACC[A/C]CAAAACAAAGTTTTT	57674
rs376697766	snp	A/G	1.67178e-05	0.00289113	missense	RNF213	GRCh38.p7	17:80340146	GAAGACTACCAGCTC[A/G]TCATGGTCTGTGATG	57674
rs376710436	in-del	-/GCACTCACCTGGCT			intron-variant	RNF213	GRCh38.p7	17:80279228	AAACTTAACCTGGCT[-/GCACTCACCTGGCT]AAAGCTCCACCAGCA	57674
rs376714317	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393331	TTTAAATGCTCTCTT[C/T]TTTGGTTTTTCAGCC	57674
rs376754230	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368943	CACCAGGCAAGCCCA[A/G]TGGATGGGTTCTTTG	57674
rs376767896	snp	A/G	0.000153988	0.00877328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363144	ACTAGGAAACTGAAA[A/G]CGGCGTCAGAAGCGC	57674
rs376768154	snp	A/C/G	0.000298542	0.0122143	intron-variant	RNF213	GRCh38.p7	17:80344038	CTGTGGGGCGTTTTC[A/C/G]CCTGGCGTGGGGGGC	57674
rs376776051	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF213	GRCh38.p7	17:80347329	CCAAGCTTTGGACAT[C/T]TTTCTGGCCAATTTG	57674
rs376778894	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360823	CCACGTTTACTTATC[A/G]TACCATTTGGAAGAC	57674
rs376786732	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80289788	GCTGCTGTGAAAAAC[A/G]AGAAGGAGCAAAAAA	57674
rs376793820	snp	A/C	3.29685e-05	0.00405995	missense	RNF213	GRCh38.p7	17:80290703	TCAAAATGGGACAGC[A/C]ATATCTGTGAGCTGC	57674
rs376794931	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364124	GCAGGACAGGCCCTC[A/G]GGGCCAGAGTCCACT	57674
rs376811590	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338102	ACTTGGGATTTGACT[A/G]ATAAGAAGGGCTCTG	57674
rs376828641	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269179	CTGGATGCTGCCCAC[C/T]CACATAGAGGGTGGG	57674
rs376830639	snp	C/T	0.000117549	0.00766556	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363611	TCCGTCTCCCCAGAC[C/T]CTGGACGCATTTGCC	57674
rs376835465	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355744	ACGGGAATGGGGGCT[C/T]ACGGAGGAAGAAGCG	57674
rs376837959	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80284907	CAGGCCAATCCCCCA[G/T]TGGGTCCCTATGGCC	57674
rs376851529	snp	C/T	6.61026e-05	0.00574865	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319456	ACCCTCCTCCCTCGC[C/T]AAGGGCAATGGCGCT	57674
rs376860756	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80311472	AGCAGTGCCTGTTTC[A/G]TTTTCTGTCGGCCCC	57674
rs376868230	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377780	GTCCCAACGGCCATC[C/T]TTGCTCCGTGGGAGA	57674
rs376874221	snp	C/T	0.000181601	0.00952719	synonymous-codon	RNF213	GRCh38.p7	17:80348169	CTCGCTGGGCGGGTT[C/T]GCAGCGGAGTGGCTG	57674
rs376888661	snp	C/T	0.00130341	0.0254952	missense	RNF213	GRCh38.p7	17:80340083	AGCTACGAGGTGGCA[C/T]GCCAAGCGGAGGAGC	57674
rs376894978	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80314413	AGGTGGTGGTGGTGG[A/T]GGTGGTGGAGGTACT	57674
rs376899584	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286544	GGCCGACCGTCAGCC[A/G]AGGGGCTCCTGAAGT	57674
rs376901868	snp	A/C/G	0.000291753	0.0120747	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288037	CCACTGGAGGGTGAC[A/C/G]GCCTCTCCGCGCCCA	57674
rs376916186	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80263099	TGGTCTGGTTTGATG[A/C]CATCCACCGCAGAGG	57674
rs376926295	snp	C/G/T	1.6869e-05	0.00290417	intron-variant	RNF213	GRCh38.p7	17:80298542	TAGAGTTGTGCTTAT[C/G/T]TACATGAATCTGGGA	57674
rs376927318	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311612	TGCCTGTATCTTCCC[A/G]CCCTGGCCCTTCCCA	57674
rs376959196	snp	A/G	0.00053203	0.0163013	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375910	GTTCAAAGTCTCAGT[A/G]TTTGGAGGGATTTTA	57674
rs376972914	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314082	GTGATGGTGGTGGTG[A/G]AGGTGATGGTGGAGG	57674
rs376977227	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270064	CAGAGCAACACTGTA[A/G]ACTGGTGTGTCCTCT	57674
rs376978506	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281023	GGTGTCTAGACCATG[A/G]GCTCAGCATTTGGGT	57674
rs376986183	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363993	GACACGAGAGGCGGC[C/T]GTGCATTCAGGGAGC	57674
rs377018287	snp	A/C/T	0.000316174	0.0125693	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358257	CTGGTTCCTCTGACC[A/C/T]GTGGTGGCCCATCTC	57674
rs377029201	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379294	AGTGCCACAGGCTAG[C/T]GTGATAGATGGAGGG	57674
rs377041958	snp	A/G	0.000153988	0.00877328	missense	RNF213	GRCh38.p7	17:80309025	CGGGGCAGGATTCCC[A/G]AGGAGGCCTTGTCAC	57674
rs377043233	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359505	CTAGCCTGGGTGGTG[A/G]CAGAGTGAGACTCTA	57674
rs377081808	snp	A/G	0.00182253	0.0301321	synonymous-codon	RNF213	GRCh38.p7	17:80339350	CTTGGACCTGGTGAC[A/G]GAGCTTAAAGAAGGT	57674
rs377084551	snp	A/C	0.000193981	0.00984647	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376830	GCTGAGCAGCAGCAC[A/C]CAGGTGACAAGCTCA	57674
rs377089311	snp	A/C			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321505	TGTATGTCTTCATTT[A/C]TCCTGGGTGTATACC	57674
rs377092593	in-del	-/GA			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398726	AGAGAGAGAGAGAGA[-/GA]AAGAGACAGAGGCAA	57674
rs377096704	snp	C/T	4.94197e-05	0.00497066	missense	RNF213	GRCh38.p7	17:80345234	GGAAGAGGTGGGAGT[C/T]GGAGCCTCACCCATA	57674
rs377102828	snp	C/T	0.000610546	0.0174614	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369480	ACACCATCCACCTGT[C/T]TTCTGTTTCTCGTGT	57674
rs377123027	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80290813	TTTAAAAAAATTTTG[-/T]TTTTTTTTTTTTCTG	57674
rs377147411	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324049	TATCATCTGTGAATA[A/G]AGTTTCACTTCTTCC	57674
rs377152382	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80300984	ACTTTTTAATGAGGT[G/T]GCTTGTTTTTTTTTC	57674
rs377163517	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366172	GCTGGCTCCCTCGGC[C/T]GGGCAGGAAGTTGTC	57674
rs377183895	snp	C/G	3.31246e-05	0.00406955	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389137	ATGCCAGAAACCCAG[C/G]CCACAGACATCCCTC	57674
rs377196511	in-del	-/AAAA			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354819	TCATACTAAAAACTT[-/AAAA]AAAGTAAAACATCTG	57674
rs377200756	in-del	-/AT			intron-variant	RNF213	GRCh38.p7	17:80324711	TTATTCATTTTTGGT[-/AT]TTTTCATGATATGAA	57674
rs377208479	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366332	TGTATTGTTTTCCAC[A/G]GGGGCTGCAGCATCT	57674
rs377269964	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282001	AGCTGGGACTATAGG[C/T]GCCTGCCACCACACC	57674
rs377291602	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376750	GCTGTTCTGTTTTCT[C/T]CACAGACAGCTTGAG	57674
rs377303933	snp	A/G	4.95315e-05	0.00497627	missense	RNF213	GRCh38.p7	17:80348141	CCGATGCCGTGGTCC[A/G]GCTGAGCGCCTACTC	57674
rs377305462	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355712	AATGGGGGCTTACAG[A/G]GGAAGAAGCGGGGTG	57674
rs377314436	snp	C/T	0.000153988	0.00877328	intron-variant	RNF213	GRCh38.p7	17:80294703	AGGTAGGCTCTTGTT[C/T]CTTCTGTCCCTCTTA	57674
rs377314891	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80291712	CATTCCTTACAAGTA[C/T]GTCATTTATAATGGG	57674
rs377329982	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80303153	CCTTGTGGAGCTTGC[A/G]TTCTAGCTGGAGAGG	57674
rs377349704	snp	C/T	0.000428852	0.014637	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388718	ACCTGATCCTGTGCA[C/T]GGGGCTTTCTGCCTT	57674
rs377352825	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307993	CATATGCCTGGTGGG[C/T]GTTCTGCATTTTTTT	57674
rs377354508	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370014	CAGCCTGGTTACTTG[C/T]ACTGGTTGTGTATTC	57674
rs377356572	snp	C/T	0.00229879	0.0338247	missense	RNF213	GRCh38.p7	17:80291822	CTTCACTTCTGGGCT[C/T]AGGAGGTAAGTCGTG	57674
rs377357981	snp	A/G	1.81345e-05	0.00301113	synonymous-codon	RNF213	GRCh38.p7	17:80317244	TGGCTGGAAGGAGTC[A/G]TTGCTGGGAGACATG	57674
rs377358867	snp	C/T	0.000999833	0.0223364	intron-variant	RNF213	GRCh38.p7	17:80332670	GGGGGTTTGGAGGGG[C/T]GTCCTGCCTCAGCCT	57674
rs377401369	snp	A/G	0.000110363	0.00742761	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381778	CAGCACAACGGCAGC[A/G]CAAGCAGGCTCGCTG	57674
rs377403761	snp	A/T	0.00032752	0.0127927	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353480	GTGCCACCTTCTGAG[A/T]GGTAACGCAATCACG	57674
rs377417776	snp	C/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80318696	CTCCTGCCTCAGCCT[C/G]CCGAGTAGCTGGGAC	57674
rs377419916	snp	C/T	1.64901e-05	0.00287137	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364500	CTAGGAACCGAGAGC[C/T]GCGTCCCCGAGTTAC	57674
rs377426343	snp	C/T	0.000153988	0.00877328	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288123	CACAGGAAGTGAGGC[C/T]CAGAGCAGCCCGCAA	57674
rs377465265	snp	C/T	0.000971857	0.0220224	synonymous-codon	RNF213	GRCh38.p7	17:80347677	CGAGAGCCTCTACGA[C/T]GCACTCAACCAGTAC	57674
rs377477759	snp	A/G	3.48426e-05	0.00417374	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374603	AGGTAGGATGGGCCC[A/G]TGGCTTCTCTCTGAT	57674
rs377483075	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294499	CTCATTACTGTGGGA[C/T]GTCTAGGATGTCTGT	57674
rs377487562	snp	A/G	1.81952e-05	0.00301617	missense	RNF213	GRCh38.p7	17:80317221	GAAATCCAATTCCCC[A/G]CGGAGCATGGCTGGA	57674
rs377488728	snp	C/T	0.000406318	0.0142476	missense	RNF213	GRCh38.p7	17:80347271	CTTCCCCGCAAGACA[C/T]TGCACAGGCTGTCCT	57674
rs377491561	snp	A/C	1.65105e-05	0.00287315	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386667	CTGGCCTGGACGCTG[A/C]GCGCTGTCTTTCTGC	57674
rs377493355	snp	A/C/T	3.29561e-05	0.00405921	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361773	TCTTTCAGCAGACTC[A/C/T]TCTGGGCAGGTTTCT	57674
rs377508377	snp	A/G	0.000655834	0.0180966	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363829	ACTGCTTCATCTGGC[A/G]CGCGCTCACCAGGAG	57674
rs377581990	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80275672	TTTATTTTATTTTAT[G/T]TTTTTTTGAGATGGA	57674
rs377600251	snp	A/G	3.30677e-05	0.00406605	synonymous-codon	RNF213	GRCh38.p7	17:80289721	AGTCGGTAAGAATGA[A/G]CAAGGGGAGCCTGAA	57674
rs377609109	in-del	-/TG			intron-variant	RNF213	GRCh38.p7	17:80290428	GCGTGTGTGCGAGTG[-/TG]CGCGTGTGTGCATGT	57674
rs377617007	in-del	-/CT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384261	CCGCTCTGTTCCTCT[-/CT]GTCCACAATGCTGGA	57674
rs377631090	snp	G/T	4.94686e-05	0.00497311	intron-variant	RNF213	GRCh38.p7	17:80309207	AGGTATCACACCCGG[G/T]ATAGGTGCGGAATTT	57674
rs377637410	snp	A/G	4.57561e-05	0.00478288	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372954	ACCAGCCACTCACCC[A/G]CTTTCTCGTTGGCCT	57674
rs377638795	snp	A/G	3.33834e-05	0.00408541	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389349	GCAAATGGGTGATCA[A/G]ACGATTCACGTGTTA	57674
rs377640343	snp	C/T	4.94173e-05	0.00497053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377729	CATTGGGTGAAACCT[C/T]ATTAGCCAATGTGTG	57674
rs377644378	snp	C/T	4.96866e-05	0.00498406	synonymous-codon	RNF213	GRCh38.p7	17:80346480	CTTTCCGAAACCGTA[C/T]GACGACAGCAGGCTG	57674
rs377645758	snp	A/G	6.59381e-05	0.00574149	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358312	CTGGAAGCGGGTCCA[A/G]GGTGCTGTCACCCCT	57674
rs377656294	in-del	-/GTG			intron-variant	RNF213	GRCh38.p7	17:80290455	CATGTGTGTGTGCGA[-/GTG]CATGTGTGTGTGCAC	57674
rs377665672	snp	A/G	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393261	GCTGGGCTTACACAC[A/G]TGAGCCACACAGTGC	57674
rs377668916	snp	A/T	1.64917e-05	0.00287151	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386737	TGCATGTCATCAGTT[A/T]TGAAGTGGAGCGGGA	57674
rs377673564	snp	C/G	0.000417401	0.0144404	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375713	ATCTCAAAAAAAAAA[C/G]ATGTGTTGAGCTTTT	57674
rs377709168	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354915	AGTCATGAAGTTAAA[A/G]TGACGTGCAGAGCAG	57674
rs377710139	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80315010	TGAAGGTGATGGTGG[A/T]GGTACTGGAGGTGAT	57674
rs377712934	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80304406	AGCACTTTGGGAGGC[C/T]AAGGCAGGTGGATCA	57674
rs377716382	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80276759	CCAAAAGTTACGCAT[A/T]AAATTATCCTAGGCC	57674
rs377718686	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371025	TTTTTTTTTTTAAAA[C/T]GTAGAATACAAATGT	57674
rs377719295	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266790	TACAGGTGTGAGCCA[C/T]CCACCGCACCTGGCC	57674
rs377733851	snp	C/T	1.68493e-05	0.00290248	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371913	TCAGGAATATTTGAC[C/T]CTGTTAAAAAAGAAA	57674
rs377760420	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385043	CCCTTCTCCAGGAAG[C/T]AGAGCTGAGGCTGGT	57674
rs386799762	in-del	A/GT			intron-variant	RNF213	GRCh38.p7	17:80271158	GGCTCAGAATCCCTG[A/GT]TGTAGGTGAAACAGC	57674
rs386799763	multinucleotide-polymorphism	CA/TG			intron-variant	RNF213	GRCh38.p7	17:80278971	CATGCTGGCACAGCC[CA/TG]GCACGGCCACCTCGC	57674
rs386799764	in-del	CACCCCTCTCATCCCACTCACACATACCCAACACACACACAG/TGC			intron-variant	RNF213	GRCh38.p7	17:80281526	ACCCCAACACACACA[lengthTooLong]CCCACTCATACCACT	57674
rs386799765	in-del	CCC/TG			intron-variant	RNF213	GRCh38.p7	17:80281589	ACACCACTCACACAC[CCC/TG]CCAACACACACAGCC	57674
rs386799766	multinucleotide-polymorphism	CTC/TAT			intron-variant	RNF213	GRCh38.p7	17:80281640	CACCCCCAACACACA[CTC/TAT]CCCACTCACCCCACT	57674
rs386799767	multinucleotide-polymorphism	GCT/TCC			intron-variant	RNF213	GRCh38.p7	17:80282254	ACACGGTGCGGTGTT[GCT/TCC]CTTTGTGTTCTTTGT	57674
rs386799768	multinucleotide-polymorphism	CAC/TAA			intron-variant	RNF213	GRCh38.p7	17:80296166	CAGGGACTACAGGTG[CAC/TAA]ACTACCACACATGGC	57674
rs386799769	multinucleotide-polymorphism	CA/TG			intron-variant	RNF213	GRCh38.p7	17:80302320	TGTTTGAGATAGATA[CA/TG]CTAATTACCCTGATT	57674
rs386799770	multinucleotide-polymorphism	CCAAGGCA/TCTGGGAG			intron-variant	RNF213	GRCh38.p7	17:80304612	ACCACTGCACTCCAG[CCAAGGCA/TCTGGGAG]ACAGAGTGAGACTCC	57674
rs386799771	in-del	AC/GTGAT			intron-variant	RNF213	GRCh38.p7	17:80313638	GTGGAGGTGATGGTG[AC/GTGAT]GGTGATGGTTGTGGA	57674
rs386799772	in-del	AGGTA/TG			intron-variant	RNF213	GRCh38.p7	17:80315908	TGAAGGTGATGGTGG[AGGTA/TG]ATGGAGGTGGTGGTG	57674
rs386799773	multinucleotide-polymorphism	CGG/TGT			intron-variant	RNF213	GRCh38.p7	17:80318634	GCTGGAGTGCAGTGG[CGG/TGT]GATCTCGGCTCACTG	57674
rs386799774	multinucleotide-polymorphism	AC/CA			intron-variant	RNF213	GRCh38.p7	17:80322152	GCCCCTCATCCCCCC[AC/CA]CCCCCCCTTTTTTTT	57674
rs386799775	in-del	ACAC/CACTTTG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360327	AGTTTTTAGTTTTCA[ACAC/CACTTTG]TTTGTGCAGTAAGCG	57674
rs386799776	multinucleotide-polymorphism	CGC/TGT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378724	TCCATGAAATGAGGA[CGC/TGT]TGAAATAGAGTCTAT	57674
rs397514563	snp	A/G	3.29484e-05	0.00405871	RNF213, LOC100294362	17	allele_origin=G(germline)/A(germline)	17:80368025	GTCTGTCTGCCCTGC[A/G]ACCACGTGCACTGCC	57674
rs397707240	in-del	-/A			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395253	CAAAAAAAAAAAAAA[-/A]TGAATTTTATTTTAC	57674
rs397733451	in-del	-/TT	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356935	GGGTTTTTTTTTTTT[-/TT]CGAGACAGAGTCTCA	57674
rs397746828	in-del	-/A			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399139	AGGAAAAAAAAAAAA[-/A]GGATGATTTAACTTT	57674
rs397787282	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377450	ACAAAAAAAAAAAAA[-/A]TCAAGGAAAATAGAA	57674
rs397807243	in-del	-/A	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392617	GGGCGACAGAGCGAG[-/A]AAAAAAAAAAACCCA	57674
rs397856903	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80338658	CCAATTAAAAAAAAA[-/A]GATAATTTAAAAAAA	57674
rs397941239	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375553	AAAGAAAAAAAAAAA[-/A]GAATTAGCCGGACAT	57674
rs397949762	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80318591	ACTTTTTTTTTTTTT[-/T]GAGACGGGGTCTCGC	57674
rs397968636	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374024	AAAAAAAAAAAAAAA[-/A]GAGGCTTCAAGGCCT	57674
rs397972165	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80291279	TTTTTTTTTTTTTTT[-/T]AGAGAGGGGATCTTG	57674
rs398031734	in-del	-/A	0	0	intron-variant	RNF213	GRCh38.p7	17:80267837	CCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGA	57674
rs398031735	in-del	-/A	0	0	intron-variant	RNF213	GRCh38.p7	17:80334628	AAAAAACAAACAAAC[-/A]AAAAAAAAAAACCTC	57674
rs398041947	in-del	-/A	0.5	0	intron-variant	RNF213	GRCh38.p7	17:80298829	AAAAAAAAAAAAAAA[-/A]TTAGCCAGGTGTGGT	57674
rs398041948	in-del	-/T	0.5	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356019	ATGCTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC	57674
rs398070977	in-del	-/TG			intron-variant	RNF213	GRCh38.p7	17:80290421	GTGTGTGCGTGTGTG[-/TG]CGAGTGTGCGCGTGT	57674
rs398100644	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80271160	CTCAGAATCCCTGGT[-/T]GTAGGTGAAACAGCA	57674
rs398120062	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382199	TGTTAAAAAAAAAAA[-/A]GCTATAAAATATTGT	57674
rs527239020	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266221	CCGAGGTGAGTAGAT[A/C]GCTTGAGCCCAGGAG	57674
rs527278359	snp	C/T	0.0150606	0.0854603	intron-variant	RNF213	GRCh38.p7	17:80342300	TCACAATGCATTTTT[C/T]AGAACGTGTCCCTAG	57674
rs527312250	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341875	GCAATGGCACGATCT[C/T]GGCTCACTGCAGCCT	57674
rs527313801	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80301201	TTTGGTATTTTTGTC[A/G]TGAAATCTTTGCCCA	57674
rs527340502	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290843	GAGACGGAGTCTTGC[C/T]GTGTCACCCAGGCTG	57674
rs527363685	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260065	TGGTCACACCATGAG[A/C]CTCACAGATGGGAAA	57674
rs527397145	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372338	GGTTCACTTTTCCCC[G/T]CCTTCTTGTCCTTAA	57674
rs527425658	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259482	AAAAACAAACAAACA[A/G]TAAATAAAGTGCCAC	57674
rs527433585	snp	G/T	0.000114175	0.00755476	missense	RNF213	GRCh38.p7	17:80336324	TGCATTCATGAAGCA[G/T]CTGAAAAAGCTGTGG	57674
rs527441921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311563	TCACAGCAGCACCTG[C/T]ATCCTGGTCCCTCTT	57674
rs527443924	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387213	TGGGCTCAAGCGATC[C/T]TCTCACATCAGCTTC	57674
rs527444921	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329184	CACGCCCCCCTCCCC[C/T]GCTACTCACTCCTGC	57674
rs527457046	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381878	CACACAGAGAGAAAA[C/T]CGTGTCTAGGGAAGG	57674
rs527481424	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80281080	GTCACACACACCCCC[C/T]GCCACACATACCCCA	57674
rs527491840	snp	A/G	8.27876e-05	0.00643327	synonymous-codon	RNF213	GRCh38.p7	17:80346477	GTTCTTTCCGAAACC[A/G]TATGACGACAGCAGG	57674
rs527564056	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80306894	CATGTGATGCACTTC[A/G]TAGCTGCCATTCTTC	57674
rs527573240	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377102	CATTCTACCGGTGGC[A/G]TCTGCAGAAGACGAA	57674
rs527600839	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311846	AAGATCACACACTTG[G/T]CTGGGTGTAGTAGCT	57674
rs527607413	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382093	CTACCATGCTGGGAG[C/T]ACGTGTCGTCCACAC	57674
rs527610055	snp	G/T			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383773	ATATATGGTGACCCA[G/T]TGACCTTCCTGCCCC	57674
rs527621120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276399	GCCACCACGCCTGCC[C/T]TATTTTTTATTTATT	57674
rs527622135	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80311731	CTTGCCCAGCTGCCT[C/T]GAGGCGTGGGCCTCT	57674
rs527655853	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80258841	GCTGAGCAGCACTCC[A/G]GCCCAGCACTATTAC	57674
rs527657548	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321649	GCTTCCAGGTTCTCC[A/G]CATCCTCACTAACAT	57674
rs527659366	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328295	GCATTTGTTGCTGTA[C/T]TGGGTTACTTTATTG	57674
rs527666790	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396336	TTATGAGACTTTGTG[C/T]ATGTGTTAACCGAGA	57674
rs527671441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285567	CTCAGCAGGTCCCCC[A/G]GCAGCTGACCAGCCT	57674
rs527678872	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384064	TTGAATAGGATGTAG[A/C]AGAAGACTCAGGGCT	57674
rs527696692	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334932	CACCTGGCCTTTTTT[A/T]TTTTTTGAGACGGAG	57674
rs527700001	in-del	-/TTT	0.00145507	0.0269336	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383651	ACCTCACTTCCAGAA[-/TTT]TTTTTTTCATTTTCT	57674
rs527727083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365404	AGGTACCAGCTCCCC[A/G]GAGGCTGGCACGGAG	57674
rs527729816	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360482	GTGATGGCCAGGGAT[A/G]TGGCGAAATGGGGTG	57674
rs527767678	in-del	-/CATC			intron-variant	RNF213	GRCh38.p7	17:80269534	CATCCTCTTTCTATT[-/CATC]CATTCATCTATCCAT	57674
rs527776870	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317964	GCAATGGAAATGGCT[C/T]TCCATGGAGAGGGGA	57674
rs527780975	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392060	GGCGTGAGCCACTGC[A/G]CCCGGCCTGTCCTCT	57674
rs527832453	snp	A/C	1.65578e-05	0.00287726	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375900	GCAGGGCTGTGTTCA[A/C]AGTCTCAGTATTTGG	57674
rs527844265	snp	A/G	0.000297698	0.0121967	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371975	ACATGCTCTTCATCA[A/G]CTGCCTGGAGGTAAG	57674
rs527845146	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357367	CATTCATCCATCCCT[-/C]CGCCTGCCTGTCCAT	57674
rs527871855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340493	CATCTGTGGGTGTCA[A/G]TCAGGGTCTGTGCCA	57674
rs527901044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270082	TGGTGTGTCCTCTTC[C/T]AGACATCTCCTCTGC	57674
rs527918280	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80305622	TTTTTCTTTCCTTTT[A/T]TTTTTTTGAGACAGA	57674
rs527959834	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365001	AACAGAACCAAGGAA[C/G]AGGAAGCCACCATGC	57674
rs527961732	snp	A/T	0.0433465	0.140692	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371020	ATGGATTTTTTTTTT[A/T]AAAACGTAGAATACA	57674
rs527967642	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365844	TCCAGCGTGGGTCAT[-/A]AGGGCCAGGTGCCCA	57674
rs527997824	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300014	TTGTGAATTGTGCTT[C/T]AATGAACATACATGG	57674
rs528030869	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264646	ACCCACATGCAGAGG[A/G]CCCTGCTGGTCTCCC	57674
rs528037355	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385684	TCTGAAAGCTCTTCT[C/T]GTCAGCCTGACTCGG	57674
rs528062047	in-del	-/TG	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80290442	GTGCGCGTGTGTGCA[-/TG]TGTGTGTGCGAGTGC	57674
rs528073196	snp	A/G	6.66744e-05	0.00577345	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390184	CCGAGGAGCGCTTCC[A/G]CCCTCAGTGGAGGTA	57674
rs528096370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284857	TCTGGAGAGAGGAAG[C/T]GCTTCCTCAAATCTC	57674
rs528103993	snp	C/T	0.000185684	0.00963366	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355249	GTCCAAGCTTCTGTG[C/T]CAGTGATAGGTTCGC	57674
rs528109858	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266441	AAGGAAAAAAAAAGC[C/T]TTACAGTGGTCTCTC	57674
rs528139386	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366069	CTGGAAGCCTGACTT[A/G]TACCCCTACCCAGCC	57674
rs528140363	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350629	GGGCAACAGAGCAAG[A/T]CCTCATTTCTAAAAA	57674
rs528163983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375529	ACATGGTGAAACCCC[A/G]TGTCTACTAAAAGAA	57674
rs528168589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305235	CTATGCTGGAGTACA[A/G]TGGCACGATCTTGGC	57674
rs528169228	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80310810	GCCTGCCTCAGCCTC[C/T]CAAAGTGCTAGGATT	57674
rs528192694	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310413	GTGCACCACCACACC[A/C]AGCTAATTTTTGTAT	57674
rs528220666	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80322353	AATTTCTGTGGGCCG[C/G]GCATGGTGGCTCATG	57674
rs528230068	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80262590	AGCTTCTGCTCCATT[C/T]TGCTGTTTCATGGTG	57674
rs528246005	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326308	TTATAAGTTGGATAG[A/C]ATTTTTTAGAGCACT	57674
rs528256219	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289190	AGGCTGGAGAGAGGC[A/G]CCTCTGGAGGCTGTG	57674
rs528292599	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395366	TAGACATCAGCTAGG[C/T]TTTTGGGAATCGTTT	57674
rs528317839	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364109	GGGCAGGTGCACAGA[C/G]CAGGACAGGCCCTCA	57674
rs528321211	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394932	ATTCCGACTGCCTAT[A/G]AACGGGTGTGGGGGC	57674
rs528338757	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80284358	AACAAGAGTGAAACT[G/T]CGTCTCAAAAAAAAC	57674
rs528351239	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389744	AAGAATGCCTGTGTG[G/T]AGAGCACTCAGGCTC	57674
rs528371533	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359355	ACATAGTGAGACCCC[A/T]TCACTACAAAAAATT	57674
rs528373104	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80349011	GGCCGGTAGGGAGGC[C/T]GCTGGAACCGTACAA	57674
rs528415294	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326794	TACCATTCGCTTACC[C/T]GTTCACCTCATGAAA	57674
rs528437376	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80341671	CCAGCCCAAGAGGTC[A/G]AGGCTGTGGTGAGCT	57674
rs528446553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374294	GGAGGAAGCTCCCTG[C/T]GAAGAGGGCACCAGA	57674
rs528449126	snp	C/T			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363662	GCTGACAAGAAACAC[C/T]CTGAAGCCCAGTCCC	57674
rs528492291	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344233	AGCAGTGTCTTCAAT[A/G]TTTCTGTTCAATTCA	57674
rs528499776	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378064	AGTATGCCTGACCTC[A/G]AGTCCCTGGATGCCA	57674
rs528512055	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80344105	CGCGTTTAGGAGACT[C/G]CACATCTTTGCCTTA	57674
rs528543193	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80292777	CTCCTCACCTGGGGG[G/T]TCCTGGGCTTCCCCT	57674
rs528545981	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392629	TTTTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	57674
rs528553725	snp	A/C	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80298780	GACCAGCCTGGCCAA[A/C]ATGGTGAAAACCCGT	57674
rs528558163	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369149	CACGCCTGTAATCCC[A/G]GCACTCTGGGAGGCC	57674
rs528569418	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363982	AGGGTGCTGGAGACA[C/T]GAGAGGCGGCTGTGC	57674
rs528606482	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262361	TCATCAAAGAGAAGA[C/T]TGCAGAAGACAGATG	57674
rs528607966	snp	A/C	0.0678174	0.1712	intron-variant	RNF213	GRCh38.p7	17:80304539	CAGCTACTGGGGAGG[A/C]TGAGGCAGGAGAATG	57674
rs528615982	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80297781	AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA	57674
rs528617428	snp	A/G	0.000594167	0.0172259	missense	RNF213	GRCh38.p7	17:80298428	TGGAGCTGGCCCCGC[A/G]GCACAAGGATGCCTG	57674
rs528629116	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80269473	ATCCATCCATTCATC[C/T]ATTCTATCTATCCAT	57674
rs528633479	snp	A/C	0.000462481	0.0151996	missense	RNF213	GRCh38.p7	17:80332267	AGTTGCTGAGTGAGC[A/C]CGAAGAAGAATCAGA	57674
rs528641702	snp	A/G	0.030278	0.119257	intron-variant	RNF213	GRCh38.p7	17:80315110	GGAGGTGATGGTGGT[A/G]AAGGTGATGGTGGAG	57674
rs528667689	snp	A/G	1.68838e-05	0.00290544	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353981	TTGCCCACTGTGTCA[A/G]TGGCAGAAACGGATG	57674
rs528691924	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80283543	TCCTGCCTCCAGCCT[C/T]CCCGGGCTCTGCCCA	57674
rs528703990	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80283095	CTAAGCCTCACCCCC[C/T]GTAAAATTATAAATA	57674
rs528783677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379812	TCAAGATAGTACTAA[C/T]TACTCCAGTACATGT	57674
rs528845874	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398928	ACTCCAATACCACTT[C/T]GTTGTCAGTGTAAAC	57674
rs528847786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331536	TGGGATTACAGGTGC[A/G]CTCCACCACGCCTGG	57674
rs528851335	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261609	ATTTGGGTGGCAGTG[C/T]CTGTGCTTGGGAAAA	57674
rs528867722	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287760	GTTGGAGGGAAACAC[A/G]GGCTAGAGTAGAGTA	57674
rs528884515	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330558	TCAGTGTGGTTCTCC[A/G]CCACCTCCCTCTGTC	57674
rs528903045	snp	A/G	0.000114331	0.00755994	missense	RNF213	GRCh38.p7	17:80332488	CACCAGGACCAAAGA[A/G]ATTGGATCAAGGACC	57674
rs528903280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297913	AATGATCGCACCACC[A/G]CGCTGCCTTGATGAC	57674
rs528914813	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261228	CCCCGGGAAGTGGCC[A/G]GGGCACGGGGGGTGT	57674
rs528935137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362755	TTTCAGCTTTGCTTC[A/G]AAAAATAAGAAATAG	57674
rs528998140	snp	A/C/G/T	6.6228e-05	0.00575419	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363297	CGTTGGAACCATGAG[A/C/G/T]TGGCTGGATGTGAGA	57674
rs529010542	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378308	CAAAGGAAAAAGCCA[C/T]GTGTAGGCTGTGCGC	57674
rs529020118	in-del	-/AAA	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80304652	CACAAATAAATAAAT[-/AAA]TAAATAATAATAATA	57674
rs529055981	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80267217	AGCGAGACTCTGTCT[C/G]AAAAAAAAAAAAGAA	57674
rs529066045	in-del	-/CTT	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80278561	CGTCTGCAGGAGCTG[-/CTT]CTTCGTCTTCCCACA	57674
rs529071300	snp	C/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80272412	TTGTGCCACATGGCA[C/G]AGTAGGCCGACGGGG	57674
rs529081840	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80277433	GGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA	57674
rs529086514	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302064	ATATTCCCACTCATA[C/T]GTGGATGTGAAAAGA	57674
rs529112576	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80297399	AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC	57674
rs529113475	snp	C/T	0.000346829	0.0131641	missense	RNF213	GRCh38.p7	17:80348102	CTGAGGAGGCCAAAT[C/T]GATCCTGCTGAACTG	57674
rs529162036	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371371	CCCATATGCTGCAGC[A/G]ATGGGGAGCAGGGCA	57674
rs529162386	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367376	AATTTTAAAAAATTT[A/C]AAAATTTTAAAAAAT	57674
rs529200219	snp	C/T	0.000114175	0.00755476	missense	RNF213	GRCh38.p7	17:80336206	TGGCCTCCATCTCAG[C/T]GGGGGAGAATGACAT	57674
rs529218997	in-del	-/TG	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356924	ATTACCTTGTGGGGT[-/TG]TTTTTTTTTTTCGAG	57674
rs529222088	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397346	GGGAGGAGACCACCC[C/T]ACATATTGTCTTACG	57674
rs529246314	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80281996	CGAGCAGCTGGGACT[A/T]TAGGCGCCTGCCACC	57674
rs529276167	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352615	CAGTGTCCCCCACCC[A/C]TCACTAACTGTGATA	57674
rs529285798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392888	AGCCACTGCGCCTGG[C/T]CTAGGATTTTAAGTC	57674
rs529335275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377956	GGGCAATGCCAATGG[C/T]GCTAAGGGTTTCTAG	57674
rs529366505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307488	CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	57674
rs529373962	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382904	TCTATTAAACACTTA[C/T]TTAGGGTTTATTATA	57674
rs529391311	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80301686	ACTCTCATACAGTGT[A/T]GGAATGTAAATTAGT	57674
rs529405253	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80312609	ACCCAGGTTTACCTC[C/T]GGGTCAGGAGCCTGG	57674
rs529406558	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259448	CTCCAGCCTGGGGTA[C/T]AGAGTGAGACTGTCT	57674
rs529454052	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329104	CCCTGGGCTGCAGAC[A/G]TAGGGTGGAGTCTCC	57674
rs529465747	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259002	CATTTAAACATTTCG[A/T]CTAGTCATACTGAAA	57674
rs529490129	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335699	AGACAGTACAGGCTG[G/T]GCGTGGTGGCTCACA	57674
rs529524237	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357054	CTCCTGAGTAGCTGG[C/G]ATTACAGGTGCCTGC	57674
rs529544872	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361430	TAGGCTGAGGCAGGA[C/G]AATCACTTGAACCTG	57674
rs529546509	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366508	TGAGCATCCTTCATG[G/T]GCTTGTTGGGCATTT	57674
rs529563325	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268070	AAGTGATCCCCCTGC[C/T]TCTGCCTCCCAAAGT	57674
rs529614263	snp	A/C/G	6.58907e-05	0.00573948	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376378	CCGTTTTGCAACATC[A/C/G]CTCGTGGACAATTCT	57674
rs529617290	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80341248	CCGGCCTGAAGTTTA[C/T]TTCTTCTGCCCTTAA	57674
rs529641932	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371224	AGGCTCCACATTGCA[A/G]CTAACCTCTAGACAT	57674
rs529650334	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261165	GGACCCCGGCGACAT[C/T]CCCGGAGCGCAGAGC	57674
rs529670326	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382053	GGAGTCTTCAGTTCC[A/G]AAGTCAGCCCCGTAG	57674
rs529698608	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275552	CAGGACGCACTCGAA[A/G]AAGACCTGAGAAGAC	57674
rs529750492	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80286215	CGGACGCAGGCCGGT[A/G]TTGGACGCAGGCCGA	57674
rs529769101	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371140	AAAAAAGAAAAAAAT[A/C]TATTTAAAGTATGGG	57674
rs529776498	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301134	TGCTGTGCAAAAGCT[A/C]CTCAGTTTAATTAGT	57674
rs529778499	snp	A/C/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351546	TATGTAAAACTCATC[A/C/G]GAACGGGTGGCCGTG	57674
rs529790037	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80322000	AAGTGCTGGGATTAC[A/T]GGCGTGAGCCACTGT	57674
rs529796862	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293806	CACTCCAGCCTGGGC[A/G]ACAGAGGGAGACTCA	57674
rs529803527	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317571	GGATGCTGTGTTTAC[C/T]TGGCCCGCCGTGCTC	57674
rs529813665	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80349560	GGGGCAGGGTGGGGT[A/C]GTCTCTCCAATGCCT	57674
rs529834863	in-del	-/TT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80323978	TCAAATTGTGTGTGC[-/TT]GTGTGTGTGTGTGTG	57674
rs529845918	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391004	GAGGTGGAGATTGCA[C/G]TGAGCTGAGATCGCA	57674
rs529848227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350763	GCGATCCCACCACTG[C/T]AGTCCAGCCTAGGGG	57674
rs529864056	in-del	-/ATTT			intron-variant	RNF213	GRCh38.p7	17:80325971	TTTATTTATTTATTT[-/ATTT]TGGAGATGGAGTCTC	57674
rs529884335	snp	A/G	0.0494327	0.149241	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355823	AATGGGGGCTTACAG[A/G]AGAAGAAGCGGGGTG	57674
rs529895719	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396628	AGCATTTATATTGCA[C/T]TCTGCATTATTCTCA	57674
rs529899581	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356266	CTCAGCCTCCCGAAG[A/T]GCTGGGATTCCAGGC	57674
rs529915042	snp	A/T	0.0391387	0.134304	intron-variant	RNF213	GRCh38.p7	17:80274779	GGTGTGAGTGGGGTG[A/T]CTGTGGGGGATGAGT	57674
rs529932683	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391439	TCACGCCCAGCTAAT[G/T]TTTTCTATTTTAGTA	57674
rs529960965	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310969	AAAGTACCACAGACA[A/C]AGTTTAAGAATAAAT	57674
rs529961652	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351519	AAATCACGATCGCAG[C/G]GCTCTGAAGTTTATG	57674
rs529978646	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311508	CCTGCGTGCTGTGCT[C/G]TAGTCACTCCTGTGC	57674
rs529982274	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280706	GCAATTCTCCCGCCC[C/T]AGCCTCCCAAAGTGC	57674
rs529986297	snp	C/T	0.0016044	0.0282777	intron-variant, missense	RNF213	GRCh38.p7	17:80278891	AGGCCGCCAGCGTGC[C/T]TTCTGCAGACTGTGA	57674
rs530006734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381827	ACACAGCCAGTCTGA[A/G]CTCTGTCTGTGCTGT	57674
rs530029620	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390769	TTTAAATTTGATAGA[A/G]AAAGCTATCCTAGGC	57674
rs530041459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333626	TTGAACCACGGAGGC[A/G]GAGGTTGCAGTGAAC	57674
rs530046161	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388186	AGCCAGGATGGTCTC[A/G]ATCTCTTGACTTCGT	57674
rs530063138	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299888	TTCCTGCAAAGGACA[A/T]GATTTCATTCTTTTT	57674
rs530087867	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293898	AAGGAGGTGATGACC[A/G]AGTTGAGAACTAAAC	57674
rs530100712	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383161	TTGCCTGTTGCCCCT[C/T]GTAGCGGTGCCAGCA	57674
rs530132547	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388309	CTTTAGTGGCTGAAT[G/T]AATAAATGAATGGGA	57674
rs530159893	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80327550	TAACCTGAGAAATGT[A/G]TCTCCCAGCTGATTT	57674
rs530161075	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290035	CTTGTTTCCTAATAG[C/G]CCCTGGGGTCCTGGA	57674
rs530163427	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380416	CATCTCCTCTCTGCC[A/G]GACTTTAGATCCCGG	57674
rs530192727	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80338100	TGACTTGGGATTTGA[A/C]TGATAAGAAGGGCTC	57674
rs530267122	snp	A/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304595	CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA	57674
rs530288963	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375428	TGGCAGGCAGCGGTG[C/T]GGGGGCGTCTATCCT	57674
rs530291664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299304	TTGTGCAGTTTCGTT[C/T]TTTCAGCGTGCTTTC	57674
rs530293807	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80323294	ACTACCATTGCTTTC[C/T]AGTAAGTTTTGAAAT	57674
rs530306724	snp	C/G	1.6476e-05	0.00287014	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369576	TGGTGTCCACCATTT[C/G]CTTCAAGGACAACGC	57674
rs530309502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269520	TCTATCTATCCATCC[A/G]TCCTCTTTCTATTCA	57674
rs530311254	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360619	CTCAGAAGGCACGAG[C/T]GCCTGGAGCATCCCC	57674
rs530321213	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279700	TCTCGAACTCCTGGC[C/G]TCAAATGATCCACCC	57674
rs530351093	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80305203	TTTTTTTTTTGAGAC[A/C]GTTTTGGTCTCATTG	57674
rs530417521	snp	A/G			missense	RNF213	GRCh38.p7	17:80336362	TGGATAAGGACCAGT[A/G]CCTGCCCAGGAAACT	57674
rs530418517	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394820	GAGTGACCCAGACTG[C/T]AGGCAGTAACTGACT	57674
rs530422594	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354731	GTTTTTCCCCAAGAA[A/G]CACACAGTAGGTCTG	57674
rs530456546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389689	CAGAGATGGCCTTCA[C/T]AAGGAGGGAGATCAC	57674
rs530458701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359230	AGATTTATAAAGAAT[A/G]TAGAAATAAATGTGC	57674
rs530461476	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289033	GCGAGGCCTCTCTTA[A/G]GAGGTGGTGAGGGAT	57674
rs530465402	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283604	CTGGCTGGCCACTCC[C/T]CTCCTGCAAGGCAGG	57674
rs530484391	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270123	GCGCACACACACACA[C/T]GTTAATGTGAGTGGC	57674
rs530491302	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370760	GCTGTGTTCATGGAC[C/T]GCCACCCGTGCTGGG	57674
rs530498413	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80309942	TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCGT	57674
rs530514700	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319796	CCCTGTCTCCCAGGA[A/G]CAGTCTCGCAGGCAA	57674
rs530521280	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393622	CTGTCAGCGTAGCAC[C/T]GAATTCAAGACCAAG	57674
rs530551595	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368605	GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	57674
rs530587557	snp	A/G	0.00185666	0.0304119	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355208	TCTCTAAAAGACAGC[A/G]GACTCCTCCATGAGT	57674
rs530623400	snp	C/G	0.00034272	0.013086	synonymous-codon	RNF213	GRCh38.p7	17:80337955	GATGCTGATGTCTGG[C/G]AAGAAGGATCGTAAC	57674
rs530633863	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268984	AGACCCGAGATCCCC[C/T]TGGCAAACCACTGGC	57674
rs530637503	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80329953	TTTTTTCTTCTCTTG[C/G]TGGAATTCCTGTTAA	57674
rs530680138	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80266911	TCTTGCACCAAATGG[G/T]TAGCCAAGTTGTAAA	57674
rs530714074	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364205	GGTTGTGGTGGTACC[C/T]CATGCAGAGGCATCA	57674
rs530725538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369057	CTGCTGAGGTTTTGA[A/G]GACTAGCTCTAACGG	57674
rs530730502	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80292692	TCCCCCACCTGGGTT[C/T]TCTGTCTGCAAACTT	57674
rs530851821	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396500	CACACAGGCACTAGT[A/G]TGCTGAAGGAAAACA	57674
rs530892607	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374237	CCAGGTAGCGCTGCC[A/G]TCGGCAGGCATTCCC	57674
rs530920263	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80272583	TTCGTGAGGGATTTG[C/T]CCTCACGACCCACAG	57674
rs530930845	snp	C/T	3.29554e-05	0.00405914	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379692	ATTGACCACAAACCT[C/T]GGGACGGCTTTCATC	57674
rs530932118	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365563	CCAATCCCGGACACG[C/T]ACACGCCACACCAGC	57674
rs530939636	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80268388	AAAAAAAGGCAGTAC[C/T]GCATCCCCGGAGGGA	57674
rs530951604	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344074	GGTTCTTTCTGGTCT[C/T]ACTGAAGTGGAATGG	57674
rs530956136	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80322394	ATCCTGGCTAACACG[A/G]TGACACCCTGTCTCT	57674
rs530980804	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324896	TGTTTTACTATTTTG[C/T]TCTTTTTGTGGCCTT	57674
rs530989442	snp	A/G	8.79624e-05	0.00663125	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363782	CCAGGCTGTCATCAG[A/G]GAAGTCAGGTGAGAC	57674
rs530999194	in-del	-/TA	0.0138799	0.0821421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356036	GACGGAGTCTCACTC[-/TA]TGTCGCCCAGGCTGG	57674
rs531015644	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304111	AATATCTTGAAAAGT[C/G]TGCAGTAGCATTGTT	57674
rs531016676	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80283010	GCCTGATTCAATATT[G/T]TAATGTAAAACAGCA	57674
rs531052494	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376758	GTTTTCTTCACAGAC[A/G]GCTTGAGAAGTCCAG	57674
rs531065355	in-del	-/AAT	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80304656	ATAAATAAATAAATA[-/AAT]AATAATAATAATAAT	57674
rs531071274	snp	C/T	0.000145668	0.00853304	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353537	ACACCGGGCGGAAGA[C/T]GGCCATGAGGAGGCG	57674
rs531076725	snp	A/C/G	0.000245497	0.011077	intron-variant	RNF213	GRCh38.p7	17:80337545	AAGGGCAAGATCCTC[A/C/G]CTCCAACCGTGGCCC	57674
rs531090635	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299759	GTGTTGTTCCCCTCT[A/G]TGTGTCCCTGTGTTC	57674
rs531107818	snp	C/T	6.1093e-05	0.00552655	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288045	GGGTGACGGCCTCTC[C/T]GCGCCCACCGAGGTT	57674
rs531110407	snp	A/G	0.0240643	0.107019	intron-variant	RNF213	GRCh38.p7	17:80314232	ATGGTGGTGGTGAAG[A/G]TGATGGTGGAGGTAC	57674
rs531128254	snp	C/T	4.97797e-05	0.00498873	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393327	CTGTTTTAAATGCTC[C/T]CTTCTTTGGTTTTTC	57674
rs531154275	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80301419	TATTTGTCATCTACA[C/T]GTTGGATAGGGGGAT	57674
rs531156790	in-del	-/A	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394459	GTTTCGGAAAGAGGG[-/A]AAAAGAGTCCCCGAG	57674
rs531158381	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281524	ACACCCCAACACACA[C/T]ATGCCCCACTCATAC	57674
rs531161453	snp	G/T	3.29625e-05	0.00405958	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363188	TTCCTTACCGTGGGT[G/T]CACCTTGCCTACCAG	57674
rs531167509	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287708	TTAGGTACTTTGGTC[A/G]AGCCAAGCTTGATGT	57674
rs531224430	in-del	-/TGG	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80313684	AGGTAATGGAGGTGA[-/TGG]TGGTGGTGAAGGGGA	57674
rs531236397	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80302394	ATTTGTACAGATTAC[A/C]GACTGTATACTTTGT	57674
rs531252783	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372885	TGTGAATGCCTGTGG[A/G]TAGGTCCGATGCCCT	57674
rs531263995	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388781	CCAGCCTTGCCCCGG[C/G]TGTTTGCTGTGAGCC	57674
rs531283543	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80267719	TCCATAACATAAAAG[G/T]GCAAGGTGAAGCAGC	57674
rs531290956	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310794	TGACCTCAGGTGATT[C/T]GCCTGCCTCAGCCTC	57674
rs531321920	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80297311	AAAATTTAGCCGGGC[A/G]TGGTGGTGCATGCCT	57674
rs531334066	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80330492	CCAAGAGGGAGAAGC[A/G]GGCTGGCGGGCCTTG	57674
rs531347784	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267148	CTTGAACCCAGGAGA[C/T]GGAGGTTGCAGTGAG	57674
rs531363772	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312522	ACCCAGGTTTACCTC[C/T]GGGTCAGGAGCCTGG	57674
rs531364047	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306963	AATCCTGAGTTTTAT[C/G]TGTAAAAGAGGTAAG	57674
rs531364506	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296940	TGCCTCGACCTCCCA[A/T]AGTGCTGGGATTATA	57674
rs531393170	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398888	TATAATTGATAATTG[A/G]AAGTATTCTCTGTAA	57674
rs531395708	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277077	AAGCAAACAAACCAA[A/C]AAAAAAACAAAAAAA	57674
rs531407880	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80281922	AGTGCAATGGCGTGA[C/T]CTCGGCTCCCTGCAA	57674
rs531412436	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80274098	AGGGACCTGAGCGTC[C/T]GCTGGGTGCGTGTCT	57674
rs531427365	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356957	AGAGTCTCACTCTCG[A/T]CCCCCATGCTGGAGT	57674
rs531433807	in-del	-/AAAT	0.0268407	0.112694	intron-variant	RNF213	GRCh38.p7	17:80304640	GTGAGACTCCAACAC[-/AAAT]AAATAAATAAATAAA	57674
rs531445746	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367329	TTTCTCTAAAAAATG[A/C]TCTATCGCAGCAGCT	57674
rs531491005	snp	A/G			missense	RNF213	GRCh38.p7	17:80291645	ACTTGGGTCATGACC[A/G]CGTTCTTGTTGAAGG	57674
rs531492295	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382806	TTATCTTCAAAAGGT[C/T]ATTAAGTTGGTGGTA	57674
rs531510308	in-del	-/TGAA	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80302278	TGGAAGAGTGGAGTT[-/TGAA]TGTTTCCAACACAAA	57674
rs531523933	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80271401	TGCCCTCCAGATCTC[A/G]GAGGAGGAGAGGGCA	57674
rs531538248	snp	A/G/T	1.67539e-05	0.00289425	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363618	CCCCAGACCCTGGAC[A/G/T]CATTTGCCGCAATGG	57674
rs531556598	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352602	AGGCAGACCTTGCCA[G/T]TGTCCCCCACCCCTC	57674
rs531589899	in-del	-/GTTT			intron-variant	RNF213	GRCh38.p7	17:80307559	TTTGTTTGTTTGTTT[-/GTTT]TTTTGAGATGGAGTC	57674
rs531618314	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80322204	CTCGCTTTGTCACCC[A/G]GGCTGGAATACAATG	57674
rs531618903	snp	A/C/T	8.22478e-05	0.00641236	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372493	TAAAAAAATAATATC[A/C/T]TTTTCTTTCTTGTTC	57674
rs531624341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301925	GAAAGTGTTGTCTAT[A/G]TACACAGTAGAATAC	57674
rs531653359	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377915	GAGCACAGGCTCACC[A/G]AGGACTGCCCAGGGT	57674
rs531679406	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392794	AGGGTTTCTCCATGT[C/T]GGCTAGGCTGGTCTC	57674
rs531696037	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80307864	GTCTGTTTTTTTTTT[-/C]TTTTTTTTTTTTAAA	57674
rs531703740	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80322585	TGTCTCAAAAAAAAA[A/G]ATTTTTTTTCGTAGA	57674
rs531711817	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80318659	GCTCACTGCAAACTC[C/T]GCCTCCCGGGTTCAC	57674
rs531725121	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397311	TTCCTCGTCTGTGAA[A/G]TATCTGTCAGTGCTC	57674
rs531746100	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80328973	AGATGCTGTTTTCAC[C/T]GCGTTAATGATACGC	57674
rs531748113	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80269452	TATCTATCCATCCAT[A/C]TATTCATCCATCCAT	57674
rs531797230	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352029	CCAGCTAATTTTTGT[A/G]TGTTTAGTAGTGACG	57674
rs531811961	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80270833	GGGGTTCAAGTGTAC[C/T]AGGGCTTTGCTCCAT	57674
rs531822913	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285790	ATTCTCCTGCTTCAG[C/T]CTCCCAAGTAGCTGG	57674
rs531835907	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264679	CCTCCACGCTGCATG[C/G]TGCCTTCCTGCTTCC	57674
rs531837936	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294566	AGGAGTCTGGCTGTC[A/G]TCAGTGTGTGGGTTT	57674
rs531864967	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296071	GTGGCCCAGGCTGGA[A/G]TACAGTGGCGCAATC	57674
rs531865359	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396788	ACACCTAATCACCCT[C/T]TCTGCAGGATATGCT	57674
rs531867684	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318349	TGGGGTTTTGCCAGG[C/G]ACCCGCCCCTGTCTG	57674
rs531894698	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371783	ACACACACACACACA[C/G]GACAGACGACCGATA	57674
rs531937100	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80291564	CTCCATGCTACGTTT[C/G]AGAATAACTAAAATT	57674
rs531943501	snp	G/T			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376402	CAATTCTGTGCCATT[G/T]TTGAGGGCGGGGCCT	57674
rs531946326	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334582	TCCAGTAGATTTTTA[C/T]TGGAGGACAAGGAGA	57674
rs531953776	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341122	TTTTGTATTTTTAGC[A/G]GAGACAGGGTTTCAC	57674
rs531962066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300433	CTTTTTAGTAGAGAC[A/G]GGGTTGCACCATGTT	57674
rs531970066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381235	CTCTGGTCCACATCT[A/G]GGAGTAGAGAGGCTG	57674
rs531981663	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274326	AGATTCCCAGTTGGA[C/G]CACTAGGCGAGGCTT	57674
rs531994157	snp	G/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80346110	ACGTTGCTGAAAAGC[G/T]CTACATCCAGCAGAT	57674
rs532058954	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370463	TTTAAAAAACATGTT[A/G]ATACTTATGATGATG	57674
rs532077936	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80288947	CAGCGGTGAGAAGAG[C/T]GTGGAGGGAGGGAGA	57674
rs532090952	snp	C/T	0.000804937	0.0200455	intron-variant	RNF213	GRCh38.p7	17:80328312	GGGTTACTTTATTGG[C/T]GTTCTTATTTTCCAG	57674
rs532111109	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354786	GGACTCTTCCTCTAA[C/T]TTCGTGTTTACAGTT	57674
rs532147105	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259332	AATTAGCCAGGCTTG[A/G]TGGCGGGCGCTTGTA	57674
rs532150164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327510	GGAAGTCAGTCCATC[C/T]GTATACTGAAGGGGA	57674
rs532170618	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355266	AGTGATAGGTTCGCT[C/T]TGGGCCTACAGCCAG	57674
rs532182534	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320694	CGCGCCCGGCCGAGC[A/G]TAATGTTTTGAAAGA	57674
rs532186904	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326875	TTTGTTTCTTATGGT[G/T]CAGATAAGCTTCATC	57674
rs532198869	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395618	CCTGCCTGAAATGAC[C/T]TCACTGGACACAGCG	57674
rs532213287	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80297651	AACTAGCCAGGCATG[A/G]TGGCGGGCACCTGTA	57674
rs532213416	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319623	TGGCCCTGTCATCAC[C/T]GTGGCTGCTGGTTTG	57674
rs532231227	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355774	GGGGTGAATGGGAAT[A/G]GGGGCTCATGGAGGA	57674
rs532236069	snp	C/T	1.64808e-05	0.00287057	intron-variant	RNF213	GRCh38.p7	17:80306227	CACTGCGTCTCTTTT[C/T]TCCGTCCCTATTTCT	57674
rs532240745	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359917	GAAACCCTGTACTGT[C/G]AAACAGATCAGCGCC	57674
rs532279718	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259131	AAAAGCAGGTTTTAA[C/T]TGGAGACCCAGCAAA	57674
rs532308436	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364089	GTAGAAAGGACACCC[C/T]GGGCGGGCAGGTGCA	57674
rs532365562	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396175	GCTGAGGTATGAGGA[C/T]TGCTTGAGCCTGGGA	57674
rs532377096	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80348390	AGCGGTTAGGGATCC[C/T]GCAGGGAGATGCTGA	57674
rs532400927	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361074	TAATTTACTTGGACC[C/T]GGGGGTTCCTGAAGC	57674
rs532401951	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80285465	CCCCACCTGCCAGGT[C/T]TCCTCAGCACACTGA	57674
rs532413679	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80262356	GAACCTCATCAAAGA[C/G]AAGACTGCAGAAGAC	57674
rs532422602	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338902	GCAGTGAGCCGAGAT[C/G]ACACCACTGCACTCC	57674
rs532430704	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395021	GCTGGCTGTCAGGTG[A/G]CAGCTCACACCCAGA	57674
rs532470781	snp	A/G	0.000399281	0.0141238	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364477	CACTCTTCGTGGAGC[A/G]CGTGCTCCTAGGAAC	57674
rs532473268	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321424	CCATTGACGGCCATC[C/T]ATGTTGCTTCTTCGG	57674
rs532482339	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385698	TCGTCAGCCTGACTC[A/G]GCCCATCCCTGTCAA	57674
rs532514160	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80333539	TCTCTACTAAAAATA[C/T]AAAAATTAGCCGGGT	57674
rs532594954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369170	CTGGGAGGCCGAGGT[A/G]TGTGGATCACCTGAG	57674
rs532598760	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375288	AAGACTGCCCATGTG[A/G]GGCATGACCCCAGGT	57674
rs532605133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289251	CGAGCGGGGAAGGGT[C/T]GTGAACATTCTGGCC	57674
rs532606178	in-del	-/AT	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80290459	TGTGTGTGCGAGTGC[-/AT]GTGTGTGTGCACGTG	57674
rs532637873	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80324216	CCAGGTGTGATGTCA[A/C]CGTGAGCTTTTCATA	57674
rs532646235	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364145	AGAGTCCACTTCCCT[A/C]AAGGTGAGGTGGGAC	57674
rs532646645	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391475	ACGGGGTTTCTCCAC[A/G]TGGCCAGGCTGGTCT	57674
rs532656756	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80299223	TTGTCTATGTCTTAG[C/T]GTTCCAGCCAGAGAG	57674
rs532660195	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341405	CTTCTGTTCTGTTGA[C/T]TTTATCCTATCAACA	57674
rs532672279	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293347	GATTAAGACGTGAGC[A/C]ACTGTGCCCAGCCAA	57674
rs532687132	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304562	GGAGAATGGCGTGAG[C/G]CTGGTAGGCAGAGCT	57674
rs532687584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309860	TCCTGGGTTCACGCC[A/G]TTCTCCTGTCTCAAC	57674
rs532695771	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359135	GCCCCCACCCCCTTC[C/T]GCAGGCCTGATGATG	57674
rs532718131	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380415	GCATCTCCTCTCTGC[C/T]GGACTTTAGATCCCG	57674
rs532730964	snp	A/T	0.000132009	0.00812324	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352987	CGGAGATCCACCCTC[A/T]TGGTTTCTGATGTGA	57674
rs532733925	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344305	TGAATCTAGGAAATT[C/T]ATCTGTTGAAAGACC	57674
rs532738197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279290	AGAGCAGCAGGGGAG[C/G]CCAAGGGGGCTTAGA	57674
rs532750973	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80284201	ATCTGTACAAAAATA[C/G]AAAAAAAAAAAAATT	57674
rs532756992	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393932	TCTTCTTTCTTCCAT[C/T]CCCTTAAATTCTGAG	57674
rs532761214	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325691	CCCCCAGCCCCCCGC[A/G]CCCCAGGTGTTTTGT	57674
rs532764812	snp	C/T	0.000399281	0.0141238	intron-variant, missense	RNF213	GRCh38.p7	17:80278864	GAAGGAAGCAGGATG[C/T]AGCCCCGCTTGAGGC	57674
rs532806298	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80292639	GGCGCTTCCCTTCTC[A/G]CAGAGCCCTCTGCGC	57674
rs532843341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304188	GAACCTTTATTGATA[C/T]GTTTTTCATAACTTC	57674
rs532860474	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80283547	GCCTCCAGCCTCCCC[A/G]GGCTCTGCCCAACCT	57674
rs532897882	snp	C/T	8.35415e-05	0.00646249	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389351	AAATGGGTGATCAGA[C/T]GATTCACGTGTTAAA	57674
rs532919790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283149	ATTCTGGGTCAAAGA[A/G]GACTATGAAACTGTT	57674
rs532940245	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371028	TTTTTTTTAAAACGT[A/G]GAATACAAATGTGTC	57674
rs532954848	snp	C/T	0.000456204	0.0150962	synonymous-codon	RNF213	GRCh38.p7	17:80325137	GACCGCGGACAACTT[C/T]AATGACATTTTAAAG	57674
rs532988998	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358555	TATGCTCTCCCAAGT[A/G]CTGGGTGAAACGCAG	57674
rs533005390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373763	GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	57674
rs533010425	snp	C/T	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80303572	CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTGAGA	57674
rs533013302	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80292124	GAGACAGAGTCTGTC[A/G]CTCAGGCTGGAGTAC	57674
rs533027571	snp	C/T	0.000116559	0.00763321	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354069	CTGTGTGCAGAGCGC[C/T]GTGGGCATGCTCAGA	57674
rs533045340	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384684	AGGAATAAGGCCAGC[A/C]CTCGCTGCCTAAGCT	57674
rs533101080	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307976	AAATAGTCATGATAC[C/T]GCATATGCCTGGTGG	57674
rs533101218	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261283	GGCCTGCAGGTCCGC[C/T]CGGGAATCCTGCGCC	57674
rs533144062	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337474	TGAGCCCTGGGGAAG[C/T]GTGGGGAGAAGGCTC	57674
rs533184125	snp	A/G	3.32845e-05	0.00407936	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353098	GGGGGAGCAGGTGGT[A/G]GAAGGGCAGATGGCA	57674
rs533188084	snp	C/T			missense	RNF213	GRCh38.p7	17:80289693	AGGACGAGATGGCTG[C/T]TGCTGAAGAAAAAGT	57674
rs533224435	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363429	TCTTCACAAGGCACA[C/T]ACCTTAGCTGAATTC	57674
rs533228329	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80348483	CCTGGCTCTGTGCAG[C/T]GCACCATGCTGGTAA	57674
rs533233464	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80262231	TGTGGCAGGGGTAGG[A/G]GAGTTTTAAACTCTC	57674
rs533254318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379096	ACTTGGGAGGCTAAG[A/G]TAGGAGGATTGCTTG	57674
rs533272516	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378519	AGTGCAGAGTGACAT[C/G]ATCATAGCTCACTAT	57674
rs533290452	snp	A/C/T	9.93421e-05	0.00704719	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383973	TCTTTCGGTGCAGAG[A/C/T]TCCCCAGCAGGCCTG	57674
rs533312656	snp	C/T	5.00221e-05	0.00500085	synonymous-codon	RNF213	GRCh38.p7	17:80346588	GGCCTTGAAGGAGAA[C/T]GTCTTCATGATGGTC	57674
rs533321341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383463	TTAGTAAGAGAAATA[C/T]AGGTTTCTGAATCTC	57674
rs533357285	in-del	-/G	0.0186154	0.0946634	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355824	TGGGGGCTTACAGGA[-/G]GAAGAAGCGGGGTGA	57674
rs533388570	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398815	ATATATACAAGTAGT[C/T]AGAAACAACAACAAC	57674
rs533448072	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80308525	AGGCTCCTCCCGAGT[C/T]CCTACCGAGTCCCTC	57674
rs533451402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357629	TATTTAGAGAACCTC[A/G]ATGACTTGTTCTGAA	57674
rs533456607	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323003	TATCTCTAAATGTTT[C/T]ATAGTTTTAGCTCTT	57674
rs533459816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302774	CTTACATGAGAGGAT[C/T]GCTTGAGCCAGGGAG	57674
rs533481422	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394307	GTTCTGGCAGTTCTT[C/T]GCGGACTTTTTTCTA	57674
rs533484071	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265394	AGAGCACTGGTAGTG[C/T]GCAGCATGAACTGTT	57674
rs533486673	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307985	TGATACTGCATATGC[A/C]TGGTGGGCGTTCTGC	57674
rs533489372	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324329	TGGATTTTGTCAAAT[A/G]CTTTTCCCGTATCTA	57674
rs533511731	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80339488	CTTCTACACGGCAGA[A/G]CAGCTGGTTTACCTG	57674
rs533540460	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80323562	GTTAGACAGAGTCTC[A/G]CCCTGTTGCCCAAGC	57674
rs533556546	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398195	TTTTGACCTGACTTG[C/G]ATATCCTGATACTCT	57674
rs533582854	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80290334	GTTCACGTGTGTGTG[C/T]GCACGTGTGTGCGTG	57674
rs533612638	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356494	AGCTCACCTGCCCCA[C/G]GGCCAGCAGCACCCT	57674
rs533614117	snp	A/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80291241	TTTCTTTTTAAAAGT[A/T]TTCTTTCTTTCTTTC	57674
rs533615822	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80362029	TCAGCGAAGGGTGCC[A/G]GTGGGTGAAGGGGTC	57674
rs533630801	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393252	TCCCACAGTGCTGGG[A/C]TTACACACGTGAGCC	57674
rs533631638	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361525	TAAGACTCCATCTCC[A/G]AAAAAAAGGAAAAAG	57674
rs533649676	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282045	TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT	57674
rs533662092	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80319027	CTTTGGTCTACTGGT[C/G]GGGGGCAGGGAGGAC	57674
rs533707391	in-del	-/GGTGT	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374178	AGCCACCCGGCCTCA[-/GGTGT]GGTGTGGTGCGGTGC	57674
rs533721185	in-del	-/AT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357990	GAGACCCTCACATAC[-/AT]GTTTTAAAAATAAAA	57674
rs533742652	in-del	-/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381288	TCTTCATTGTAGCTA[-/G]GGGAAGAAAGAGCAC	57674
rs533775518	in-del	-/AAAAG			intron-variant	RNF213	GRCh38.p7	17:80336905	GACTCTGTCTCAAAA[-/AAAAG]AAAAGAAAAGAAAAA	57674
rs533786455	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396938	TGCTCAGGTGCTCCA[C/T]AGCCCATAAAAAACG	57674
rs533791889	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387162	GTCTCACTCTGTCAC[C/T]GAGGCTGCAGGGCAG	57674
rs533793640	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80334751	CTTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	57674
rs533795641	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80341344	AGCCATGCCTCTTGA[A/C]CCACCCTTCGTTTGC	57674
rs533800296	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80272869	CCCACCCTGGGGAAG[A/C]CAGGAGGAATGTCTA	57674
rs533825368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391939	GCCCGGCTAATTTTT[C/T]TGTACTTTTAGTAGA	57674
rs533836081	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378309	AAAGGAAAAAGCCAC[A/G]TGTAGGCTGTGCGCC	57674
rs533858189	in-del	-/CCCA	0.45889	0.13735	intron-variant	RNF213	GRCh38.p7	17:80325674	TGTGCTGTCTGATTT[-/CCCA]CCCCCCAGCCCCCCG	57674
rs533914551	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385830	GGATTCAAGCAATTC[C/T]CCTGCCTCAGCCCCT	57674
rs533934619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376155	ATATGCACAATTCTC[C/T]TCTCTGAAAAATTTC	57674
rs533957807	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391049	CCTGGGCAACAGAGG[A/G]AGACTTCATCTCAAA	57674
rs533990166	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270670	TTCCTTGAGCGGCCT[C/G]TCTGTCTTTAGGGAA	57674
rs534015004	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80305474	TGAGCCACTGCGCCC[A/G/T]GCCTGATTTTATTAC	57674
rs534023585	snp	A/T	0.00835141	0.0640778	intron-variant	RNF213	GRCh38.p7	17:80311027	GGAGTGGCTGCTATT[A/T]AAACCGCCACAGGCA	57674
rs534026018	snp	A/G	0.000798403	0.0199641	missense	RNF213	GRCh38.p7	17:80346230	GGAAAACAGAAGATG[A/G]GTGCAGCTTTGTCAG	57674
rs534028828	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359930	GTGAAACAGATCAGC[A/G]CCGTCTGCCTGGCCT	57674
rs534066171	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310532	TGCTGGGATTGCCGA[C/T]GTGAGCCACTGCACC	57674
rs534104058	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370696	CACCGGAGTAGACAG[C/T]TGCCTCACAGAAAAT	57674
rs534113405	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326549	GCCTGTGTCCACCAT[G/T]CCAGTATCGTGCAGA	57674
rs534120881	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264868	AGCCCACCACCTTCT[A/G]GCCCTTCCTGGATAC	57674
rs534139343	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395272	ATTTTATTTTACTTG[A/T]CACACCTGTCTTAAT	57674
rs534173063	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353788	AGGGGTGAGGATGGC[A/G]CCCCACTTTCCTCAC	57674
rs534174974	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395839	CTAGAACCACAGCAA[A/G]AAGAGGAGGCATGCT	57674
rs534182384	in-del	-/GTGT	0.001229	0.0247587	intron-variant	RNF213	GRCh38.p7	17:80290487	CGTGTGTGTGCGCAC[-/GTGT]GTGTGTGCGCGTGTG	57674
rs534187419	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80284743	TCTCATCAGCTGTTT[C/T]CCGTTACTCCCTCGT	57674
rs534196259	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80350128	CCATCCTCGGACCTC[A/G]TTAGGAGGCATTCCT	57674
rs534246071	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80289449	ACAAAAATTAGCCAG[C/T]CGTGGTGGCATGTGC	57674
rs534246369	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80285024	GCAGCCGATAACAGG[A/G]AGAGCCAAGGGACCA	57674
rs534261458	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80280457	GGTTTGGTGGGTTTT[G/T]TTTTTGTTTGTTTTG	57674
rs534261528	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274444	GGCAGTGTCAGCTCC[C/G]GGGTTTCTTGCTGGG	57674
rs534280009	snp	C/T	3.29614e-05	0.00405951	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374497	CAGATGGATAGGTAC[C/T]TGGTGTACGGCGATG	57674
rs534284052	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380582	TCTTAACACCCTGCC[C/T]GGGGATCAGCATCAA	57674
rs534299580	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381417	TCACCTGGATCACTC[C/T]GCCGTTTTCATCTTA	57674
rs534324003	snp	A/G	1.65575e-05	0.00287724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381011	CAGTGCTGCCAAACA[A/G]TGGGCTCAGTTAAGA	57674
rs534333539	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80273534	CTGCCCACAGGGCAG[C/G]AGCAGAGCTGCCCCT	57674
rs534338467	snp	A/G	0.0012357	0.0248258	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386393	CTACACAATGAAATT[A/G]TCTACGCCGTGGAAA	57674
rs534354213	snp	A/G/T			intron-variant	RNF213	GRCh38.p7	17:80333088	GAGTCTCGCTCTGTC[A/G/T]TCCAGGCTGGAGTGC	57674
rs534355648	snp	C/T	0.000214166	0.0103459	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369637	GCTCTCTCTCCTCTT[C/T]GTCCAAAAGGGGCGC	57674
rs534406961	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80298895	GAGGTAGGAGAATCA[C/G]TAGAACCCGGGAGGT	57674
rs534409732	snp	A/C	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80263188	CCCATTACTAGGAAT[A/C]TGACTGCCAGCCCAG	57674
rs534410425	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369345	GGAGGTTGCAGTGAG[C/T]GGAGATCGCGCCACT	57674
rs534417238	snp	C/G	3.3631e-05	0.00410053	intron-variant	RNF213	GRCh38.p7	17:80298537	AGTCGTAGAGTTGTG[C/G]TTATCTACATGAATC	57674
rs534421198	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311396	TTGTTATTGGCCATC[A/G]CTGTCCAGCCCTGTG	57674
rs534428444	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362563	AAAACAACAGCCGCC[A/G]GCCAGTGCTGCAAAG	57674
rs534439111	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374889	TTACTTCCTTTGAGA[C/T]CCTGCTGGAAAACAG	57674
rs534496333	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80278351	GGCTGGCCCTGGGGT[A/G]CCCGGGCCTGCCTAT	57674
rs534548723	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359007	TGGTTCTAGCCAGAC[C/G]CAGCATGGCGTGACA	57674
rs534567095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310016	GCCTTGGCCTCCAAA[A/G]TGCTGGGATTACAGG	57674
rs534579403	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278976	TGGCACAGCCTGGCA[C/T]GGCCACCTCGCACTT	57674
rs534595460	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80338590	GGAGTTCATGACCAG[C/T]CTGGGCAACATAGCG	57674
rs534602828	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379986	CCTTTTGGGCCTTGG[A/G]TGCACCTTCTGTAGA	57674
rs534607981	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80274003	GCCTGAGCTTCTGCC[C/G]TGTGTATCTGTGTCC	57674
rs534616033	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354307	CAGTGGGAATCTAAG[A/G]GCATCTCTCAGATTT	57674
rs534655160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261835	ACCAGCCTGGCCAAC[A/G]TGAAACCCCGTTTCT	57674
rs534658964	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80317719	ACCCCCGAAGCTCCA[G/T]AGGGCATGTTACAGT	57674
rs534665632	snp	C/T	0.00027356	0.0116921	missense	RNF213	GRCh38.p7	17:80339232	AGAGGCTCAGCCAGG[C/T]CTTCATCGACCTGCA	57674
rs534665823	snp	G/T	0.000115309	0.00759218	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367956	TTGCCCTTCTTGGAT[G/T]CTAGGTTTGGGATTC	57674
rs534722447	snp	C/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304612	ACCACTGCACTCCAG[C/T]CAAGGCAACAGAGTG	57674
rs534732262	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294114	GGGTTTTCTAATTAT[C/T]TTACAGTCAACCTCA	57674
rs534735479	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262629	CTTTATAGCCTTTTA[C/T]AAAAGGATAGCTTCC	57674
rs534749651	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80269646	CTAGCTTATCTATCT[A/G]TTCATCCATCAATCT	57674
rs534769541	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80323531	TTTCATTCAATTAGA[-/T]TTTTTTTTTTCCCCT	57674
rs534771493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298736	TTGGGAGGCTGAGAC[A/G]GGTGGATCACCTGAG	57674
rs534779903	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320104	GTCACAGATATGTAC[A/T]GTCATCACCACAGTT	57674
rs534794013	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292403	GGAAAGGAGAGAAAA[C/G/T]GAAGCCAGAAGAAGG	57674
rs534797444	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394549	TTTGATACTTAGGAC[C/G]TCTCTGGACTAATTT	57674
rs534820602	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319756	TTATTTAGCTCTTTT[C/T]GGCAAAGGGGAAGAG	57674
rs534826362	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292213	TCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAGG	57674
rs534829297	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388977	CTGCTCTCCGCATGC[A/G]GGTACTGATAGGTAG	57674
rs534836776	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300358	CAGCCTCTGCCTCCT[C/T]GGCACAAGCGATTCT	57674
rs534850961	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80325370	CTCAGAGTGTCTTGC[A/G/T]TTGTAAATAATAACT	57674
rs534885407	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80343535	TACACTAACCTAGAC[A/G]TAGAGCCCACTGCAC	57674
rs534902963	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80272614	ACCTCCCCGCAGCCC[A/T]GCCTCCCAGCACTGG	57674
rs534915309	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320551	ATGTGCCGCCACACT[C/T]GGTTCCTTTTGTATT	57674
rs534939622	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387205	TCCACCTCTGGGCTC[A/C]AGCGATCCTCTCACA	57674
rs534947590	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80337210	GCCATTGCTTCCAGC[C/G]TCACCCCCAGAGGGT	57674
rs534947679	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343709	TTTTATGGGGCTGCC[C/G]TTGGAGACATGGGCC	57674
rs534960573	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364296	AGGAAGTATGTCACA[C/T]AGGGCTTGCTTGTAA	57674
rs534971828	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296307	TTGTAGGCGTGAGCC[A/G]CCGTGCTGGGTCTGA	57674
rs534995039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373927	AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG	57674
rs535025919	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80270509	ATTTCTATTCAGATT[A/C/G]TCTCCAGCGTTCAGA	57674
rs535037014	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80268480	CCTCCCCTATTTGGC[C/G]TTTGTGGAAGACGGG	57674
rs535053529	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298140	CTGCAAAGGAGCTGA[C/T]GCCCTAGGCTGGGGG	57674
rs535085014	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323878	GTTTTCTGAATTCTG[C/T]TTCCAGATTGTTCCT	57674
rs535117223	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338806	TACAAAAATTAGCCG[A/G]GCATGGTGGCACGTG	57674
rs535165841	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353242	CAGGGCCGAGCAGGT[A/G]CGCTTACCACAGGCT	57674
rs535172187	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80303175	CTGGAGAGGCAGGCA[A/G]TTAATACATCAGTAA	57674
rs535193638	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80313337	ACCTGGCAGGGTGGC[C/T]CTGAGGCAGACAGAT	57674
rs535201980	snp	A/G	4.94222e-05	0.00497078	synonymous-codon	RNF213	GRCh38.p7	17:80319249	GGACACCAAAGGCTT[A/G]GAGGACAGTGTGGCC	57674
rs535236444	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388508	GATACACAGGGCAGC[A/G]CGGCACTACGCTGCA	57674
rs535271026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336678	TGAATGGTTGTAATT[A/G]TCATTTTATTCTGTT	57674
rs535281920	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397674	CAGGAATTGCTCACT[C/T]GGGGAGCTCAGTTGT	57674
rs535311729	in-del	-/G	0.000349174	0.0132085	intron-variant	RNF213	GRCh38.p7	17:80344046	GTTTTCGCCTGGCGT[-/G]GGGGGGCTCTTGGGT	57674
rs535319023	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367640	GCACCCCACACCCCA[C/G]ACACACGGCGCAGCC	57674
rs535329813	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297677	CTGTAGTCCCAGCTA[C/G]TCGGGAGGCTGAGGC	57674
rs535331723	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303658	AACCTTCGCCTCCCA[G/T]GTTCAAGTGATTCTT	57674
rs535359828	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381107	GGAGATAATTAGTCT[A/G]CAAAGTAATATACAA	57674
rs535375584	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80277557	GAGCCGAGATTGAGA[C/G]ACCGCACTCCAGCCT	57674
rs535398521	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366874	TATACCAACATCATG[C/T]CTGCCCATCAAATTC	57674
rs535405571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322976	TGATGAAGATTTACT[C/T]CTATGTTTATTTATC	57674
rs535405594	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387983	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	57674
rs535408662	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398342	AGCATGGGTCAAGCA[C/T]AAAGTAAGACCACCC	57674
rs535422471	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376611	TGTCACTGTAGAGAC[C/T]GAGCTGCAGCTGTGG	57674
rs535422842	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382233	CACTGAGCTAACTTT[C/G]TATTTTAAAAATTTA	57674
rs535426932	in-del	-/TATT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80269645	TCTAGCTTATCTATC[-/TATT]CATCCATCAATCTAT	57674
rs535459586	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381933	AGCACTCTGCTTGCC[C/T]AGAGGCTGGAAGGAG	57674
rs535482952	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357742	TTTGGGAGGCCAAGG[C/T]GGGAGGATTACTTGT	57674
rs535483506	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387367	CGCCTAGGCCTCCCA[A/G]AGTGCTGGGATTATA	57674
rs535507380	snp	C/T	6.61157e-05	0.00574922	synonymous-codon	RNF213	GRCh38.p7	17:80347983	ATACAGCCCCTCTGA[C/T]GTCTTCATCGGCTAC	57674
rs535538406	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352769	GGTCGTGTATAGTAT[C/T]GGGTTGGGTGGTTTC	57674
rs535539697	in-del	-/CT	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370727	CACTCATGACAAGCC[-/CT]GGGTTATCAGCCGGC	57674
rs535547697	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358151	GGAAATGTCAAGTTA[C/T]TGCTGTCGCTGTAGT	57674
rs535562990	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300690	TTCTGGGTAGCTGGG[A/G]CCACAGGCACCCCAC	57674
rs535567724	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312775	GGAGCACACAGATGC[C/T]GTTCCCTCCCTCCCT	57674
rs535593006	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366173	CTGGCTCCCTCGGCC[A/G]GGCAGGAAGTTGTCG	57674
rs535600452	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259757	TTCTTCTAGGGAAAC[C/T]TGCCGTGGGCACCGT	57674
rs535607002	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271597	GGGAGAGGTGGGGTC[G/T]TCCAGACCCAGGATT	57674
rs535634373	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80280564	GCTCAAGCAATCCTC[A/G]TGCCTCAGCCTCCCG	57674
rs535636279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286093	GTGAGTCTCCTCTGT[C/T]CACACCCAAACGCAC	57674
rs535649550	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367457	GGGGTATACAGATGG[C/T]CATTATTATTACTTA	57674
rs535662348	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80335960	CCAGCTTGGGTGACA[A/G]AGTGAGACTCTGTCT	57674
rs535665707	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266453	AGCCTTACAGTGGTC[C/T]CTCAGTGCTCAAATG	57674
rs535673041	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328541	AGGAGAACACAGTAA[A/G]AATGGATCACAGTAG	57674
rs535696127	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80285744	TGCGTAATATCGGCT[A/G]ACCGCAGCCTCTGCC	57674
rs535704599	snp	C/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353207	TCTGCAGAACTGACT[C/G]GTGGCTCATCATAGA	57674
rs535710721	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356117	AGCGATTCTCCTGCC[C/T]CAGACTCCTGAGTAG	57674
rs535723190	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362235	GAATAAACAAGTGAA[A/G]TTCAATAGAAAGTCA	57674
rs535780032	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260240	CTCTGGGCCGCTCCC[A/G]GGCTGGCCGCCGGCT	57674
rs535795767	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306647	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	57674
rs535800879	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369346	GAGGTTGCAGTGAGC[A/G]GAGATCGCGCCACTG	57674
rs535837421	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271075	CGGCCCTGATTGGAT[A/T]AGGCTAGTCAGGGCC	57674
rs535839301	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80264742	CCCCTTACAAGATCC[A/G]CCCCTGCCCCCGCTG	57674
rs535848029	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275995	TTCTTTTCCATGTTT[A/T]GGCTGTAGGTGTTTA	57674
rs535851392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264064	AGCCCACCCGAGTGG[A/G]AGGAGAGGGCAGGGC	57674
rs535904923	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394694	AAAAATACAAAATGC[C/T]TGTCCAGGACTCAGC	57674
rs535905847	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80294124	ATTATTTTACAGTCA[A/G]CCTCACTGGGTTTTC	57674
rs535918381	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360578	CTGGGGCACTGGACT[C/T]GGAAGATGCCCCCAG	57674
rs535951819	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80272936	AGGTGCCCGAGGTGC[A/G]CTGACATCCTAGTAC	57674
rs535956549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365179	CACCCGCACCCGTGA[C/T]CTTCACGTGAGCACA	57674
rs535975310	in-del	-/GAC	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80309496	ACGCCACGCGGAGAA[-/GAC]GACTTTTCTTTTTTC	57674
rs536025294	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80322306	GCAGGGACTACAGGC[A/G]TGTGCCACCATGTTC	57674
rs536043351	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396859	CAACCTGGGGCCAAA[A/G]CAGGGGGAAGCAGGA	57674
rs536048018	snp	C/G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369216	CCAGCCTGGCCAACA[C/G/T]GGTGAAACCCCATCT	57674
rs536060028	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321835	GGTTCAAGCAATTCT[C/T]CTGCCTCAGTCTCTC	57674
rs536070424	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391759	AGGATTATAAACTAG[A/C]CTTTTTTTTTTTTTT	57674
rs536108609	snp	A/G	0.000183724	0.0095827	synonymous-codon	RNF213	GRCh38.p7	17:80340277	TCACTACCGGGTCCC[A/G]AAGCAGACCCTGTCG	57674
rs536109705	snp	A/G	1.64811e-05	0.00287059	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351800	TATGTGGGCTTCCAC[A/G]GAGGTGAGATCAGAA	57674
rs536138442	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311638	TCCCAGGTATAGTGA[C/T]GCTGTGTTCCCCTGC	57674
rs536146884	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356418	AGGCCTGGCTCCGTC[A/G]TGTTCTGTGGTCACC	57674
rs536149402	snp	A/G	1.66432e-05	0.00288467	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369896	GGAGACTTGCTTCTG[A/G]AAAGCCCTGGCTTTT	57674
rs536170457	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373815	GACCAGCCTGGCCAA[C/T]ATGGTGAAACCTTGT	57674
rs536187037	in-del	-/AT	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80299461	AGAGGAATATTGGCA[-/AT]ATATATAATCCTGAT	57674
rs536222420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334688	CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT	57674
rs536239073	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377275	AGAGACGCATTCAAA[A/G]GCCCACCACAAAACA	57674
rs536243730	in-del	-/ACTGAGATTTTCCAGACGTT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80308868	ACAAGTTCAGGACTG[-/ACTGAGATTTTCCAGACGTT]AACCTAGATAAGGTC	57674
rs536286991	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300096	TAATGGGATTGCTGC[A/G]GTGAATGGTATTTGT	57674
rs536288302	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359565	AAAGAGTGAGAGAGG[C/G]AGGGAGACAGAAGGA	57674
rs536319115	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80279551	TTCACTGCAACCTCC[A/G]CGTGCAGGGTTCAAG	57674
rs536320367	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80282159	ACTGAGGCCGGCCCC[C/T]GACACCATGCACTTT	57674
rs536321935	snp	A/G	5.00371e-05	0.00500161	intron-variant	RNF213	GRCh38.p7	17:80349950	TCTCCCTCCCCAGCC[A/G]CAGCCGTGTGGCTTC	57674
rs536339383	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310157	TGTGGTGCAGAGATC[A/G]GCAATTCCTTCTTTC	57674
rs536347305	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354943	CAGGCAGGGGACAGG[C/T]GGGATTTTCCCAGTC	57674
rs536375713	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329779	GAGGCTGCAGTGAGC[C/T]GAAATCACGCCACAA	57674
rs536375808	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317076	GAGCCCTGGTGTTCG[C/T]GGAGTCCCGCGCTCT	57674
rs536398829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310489	AACGCCTGACCTCAC[A/G]TGATCCACCTGCCTT	57674
rs536402172	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396399	TTCAGGCAATTCCAA[C/T]TTAGAAACAAACTTC	57674
rs536427217	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274409	TCCTGGGCTCTAGCG[C/T]GGCCTGGGAAGACCC	57674
rs536454031	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385731	CCCAGCACTGTGTTT[G/T]TTTGTTTTTGAGATG	57674
rs536455383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279970	GCCTTCCCCGCACCG[C/T]GCTCCCCCCAGCCCC	57674
rs536458580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338418	TTGAGAATGGTGTAC[C/T]GGTCTAAGTAATAGT	57674
rs536471837	snp	A/G	9.9739e-05	0.00706113	missense	RNF213	GRCh38.p7	17:80350374	GATGGAATCCGTAGC[A/G]CCCAGCTCATTGCCT	57674
rs536477552	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80342119	TGTTTAGATATTCAG[A/T]TATTTGCCCCGTGTC	57674
rs536538753	in-del	-/TTA	0.0016937	0.0290513	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372766	TGCTTTCCTTTGGGT[-/TTA]TTAAAGACTCCGTTA	57674
rs536549278	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80299733	CTCCACCCTCTGATA[A/G]GCCCCAGTGTGTGTT	57674
rs536579478	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381276	TATTTTACCTGTGTC[A/T]TCATTGTAGCTAGGG	57674
rs536652298	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384279	TCCACAATGCTGGAG[C/G]ATGGGCAGATCAAAC	57674
rs536673413	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395736	CAGGAGCCCACTGAC[A/G]TTGGAGTGCTAAAAA	57674
rs536688968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278281	TCGGATGAGCATGCC[C/T]GCTACAGGGCCAGAC	57674
rs536692431	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80289285	GTAAGAAGCATCCCC[C/T]GTAGGGGTCAATGTG	57674
rs536710021	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390439	AGGCTGGAGTGCAGT[A/G]GAGTAATCTCAACTC	57674
rs536716139	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80305947	TCAGTAGGTTGTTCT[A/G]TACTTTTCATTTGAT	57674
rs536716372	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284999	GTAAGGCTGATGTTA[A/C]TCAAACCATGCAGCC	57674
rs536743397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317321	AGGGCGTGAAGGCAA[A/G]CTGGAGAACCCCAGA	57674
rs536746878	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304336	TTGATCCTGGACACT[C/T]GTTAATAATAATTAA	57674
rs536761262	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303809	TCCTGGCCTCAAGTG[A/G]TCTGCCCGCCTCAGC	57674
rs536783127	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385319	GCGGTGAAGGGTGCT[C/T]GAACCCCAAAAACAT	57674
rs536800737	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80290480	GTGTGCACGTGTGTG[C/T]GCGCACGTGTGTGTG	57674
rs536808015	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374822	GTTGACAGATTTGCT[A/G]TGTCTTGCTGATCTG	57674
rs536835119	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80262519	CAGGCACTCCTCTTG[A/T]GTGTCCCTGGGACCG	57674
rs536872282	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394086	ATCTGACCCTCTCCC[C/G]TCACAGTGAGCCACT	57674
rs536873602	snp	A/G	5.85257e-05	0.0054092	stop-gained, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287934	GCTTTCAAACCCGTG[A/G]CCTCAGGACACAGCC	57674
rs536874435	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80271814	AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAA	57674
rs536900376	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80283307	GAGGGGGTGAGCCTG[C/G]GGCTGCTGCTCCGAG	57674
rs536906319	snp	C/T	0.00199481	0.0315187	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80288906	GTGCTCACATTCCAG[C/T]GGAGAGAGAGTCAGG	57674
rs536922113	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364188	GGATCATGCAGTGAG[C/T]GGGTTGTGGTGGTAC	57674
rs536937241	snp	A/T	0.0279526	0.114869	intron-variant	RNF213	GRCh38.p7	17:80315676	GTGGTACTGGAGGTG[A/T]TGGTGGTGGTGAAGG	57674
rs536960788	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363929	CACCCGTTCACTCCG[C/T]ATTTGCCGAACCCTT	57674
rs536962601	in-del	-/TT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80323531	TTTCATTCAATTAGA[-/TT]TTTTTTTTTCCCCTG	57674
rs536991140	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80333080	TTGAGATGGAGTCTC[A/G]CTCTGTCGTCCAGGC	57674
rs537000780	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367109	GGTACAGGAGTGATC[C/T]GGACCTAAGGTATCA	57674
rs537006789	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80296644	GCCTTTCCTGACCAG[C/G]ATGTCTTATCACGAC	57674
rs537018904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379500	AAACAAGCACACACT[A/G]GGACAATCTGAGGGT	57674
rs537027553	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80337166	TACTTGGGGACCACA[C/G]AAGGACACTGAGGAC	57674
rs537032919	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349321	CAGCAGGCCTCGAGG[A/G]ACGTTTCGACTTGCA	57674
rs537038492	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267942	CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT	57674
rs537050956	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267443	CGAGACTCCATCCCA[A/G]AAAAGAAAAAAAGTG	57674
rs537069745	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348903	GTGACTCTGCAGAGC[C/G]ACATCTCAGCCCTAT	57674
rs537080283	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80323908	TTGCTGGTGTCTAGA[C/G]ACACAGTGCTCCATG	57674
rs537133079	snp	A/G	3.29468e-05	0.00405861	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367879	TGGATCTGTGAAGGC[A/G]AGAATTCTGAACCTC	57674
rs537134259	in-del	-/AGAA	0.0232847	0.105357	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359611	GAGCGAGAGAAAGAG[-/AGAA]AGAAAGTAAAGAAAG	57674
rs537145168	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80294584	AGTGTGTGGGTTTTT[A/G]CTTTTCCCTTCCTCC	57674
rs537172430	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80297528	GGAGGCTGAGGCAGG[A/T]GGGATTGCTTGAGCC	57674
rs537182624	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261364	CTTTTACGAGGGAGG[C/T]ATCGCCCCGTCTGAA	57674
rs537196082	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80282484	GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC	57674
rs537198988	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312668	GGGAGTCTGCAGGGC[C/G]CCTCTCTGGGGCGTG	57674
rs537203179	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365341	AGCGGCTTAGACACA[A/G]TATCAGCTGATTTCC	57674
rs537205707	snp	A/G	0.000117682	0.00766988	missense	RNF213	GRCh38.p7	17:80325183	GCAGATGTCAAGCAC[A/G]TCTTCAGATTGTGTG	57674
rs537234997	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393560	TCTCTCCTCGTCTGC[A/G]GCGTGGACTTGATCA	57674
rs537244247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324693	ATATGCTATATTAAG[A/G]GTTTATTCATTTTTG	57674
rs537245626	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80295308	CACTGCGGTGCAGCC[G/T]GGGTGGGTTTCAGGC	57674
rs537248710	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331651	ATCTCAGCGTCCCAA[C/T]GTGCTGGGTGGGATT	57674
rs537264833	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283851	AAGCTGCTAGAGCAT[C/T]CATGACCTTGGCTTA	57674
rs537278469	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292176	TGCAACCTCCGCCTC[A/C]CAGGGTCAAGCAGTT	57674
rs537295989	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80338959	CTCAAAAAAAAATTA[-/A]AAAAAAAAAAAAAAT	57674
rs537304842	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364650	CTGGGAGACGCTCTT[C/T]TGGCTCTGACCGTTT	57674
rs537363507	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353452	CTCCCAGATGGCACC[A/G]CTGCCAGTCCCTGTG	57674
rs537391500	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310957	TTTTCTTGTGTTAAA[A/G]TACCACAGACACAGT	57674
rs537403637	snp	C/G			missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288144	CAGCCCGCAATTCCA[C/G]GACCACACGGAAGGG	57674
rs537412085	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80322860	TCTTATTGGTTTCTT[C/T]TGAAGCACAGAAGTC	57674
rs537417309	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330149	TTTCTCGGAATGTTC[C/T]TTTTTAAATTCTGTC	57674
rs537443738	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80338960	CTCAAAAAAAAATTA[A/T]AAAAAAAAAAAAATT	57674
rs537449500	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260455	CCTCCCGGGGGCTGG[A/G]GGCCCGGAGTCACTG	57674
rs537462512	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80269691	TCATCTGTTCTATCT[A/C]TGTATCTATCTTATG	57674
rs537464563	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80290375	TGTGCGTGTGTGAGT[C/G]CGTGCACGTGTGTGC	57674
rs537478671	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302886	CCACAAACTTTCTCT[C/T]TAAGTATAATCTCTC	57674
rs537534615	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318794	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	57674
rs537536451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308511	CTGAGTCCCTCCTAA[A/G]GCTCCTCCCGAGTCC	57674
rs537549318	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80318995	GAGTGGGAAAAGAGA[C/T]TCTTTTAAATTTTAG	57674
rs537565053	in-del	-/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80274702	GGTGTCTGGGGGGGG[-/T]GAGTGGGGTGAGTGT	57674
rs537566892	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80333763	CTAGTGCACGTCCTC[A/G]AGGAAGCAACTGCTC	57674
rs537647693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382488	CTGGCATTCCTATTT[A/G]TTTTCCATTTTGAAC	57674
rs537654602	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264926	TTGCACCACCCTTCC[C/G]CAGAGGGCGGCCTGG	57674
rs537693317	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80276913	AAAAAAAAAATTAGC[C/T]GGGCGTGGTGGCGTA	57674
rs537702559	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342690	ATACTTCCATATATA[A/C]TATATATATTCTATA	57674
rs537738289	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296300	GCTAGGATTGTAGGC[A/G]TGAGCCACCGTGCTG	57674
rs537754412	snp	A/C	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80307634	GGCTCACTGCAACCT[A/C]TGCTTCCCAGGTTCA	57674
rs537770104	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398245	GTTTGGTGTAAACTG[C/T]AAAAGTGTGTGTGTG	57674
rs537770973	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383518	TATAAACAAACAACA[C/G]TGAAATTAGAAGATC	57674
rs537778315	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378043	GTGCACTGCAGGCTG[G/T]CTGGCAGTATGCCTG	57674
rs537797769	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396999	CTAAACTTACTATAA[A/G]GGTCCTACCTTCCCC	57674
rs537798475	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311182	AAAATACTCTCTACC[A/T]GTGCCATAAAAGCAA	57674
rs537831688	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397588	GCCCCCAGTCACGTA[C/T]CCCCTGCTTGCTCAA	57674
rs537842801	snp	C/T	0.00115304	0.0239831	synonymous-codon	RNF213	GRCh38.p7	17:80346300	GTTCCACGAGCACAG[C/T]GCGATGCTCTTAGCG	57674
rs537867605	in-del	-/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375965	CAAATCATACCATAA[-/T]TTTTTTTATCTAGGA	57674
rs537869841	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286232	TGGACGCAGGCCGAG[C/T]GGGAGGCTGGAGCCA	57674
rs537892215	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287364	AAAAATTAGCTGGGC[A/G]TAGTGATGCTCACCT	57674
rs537902873	in-del	-/CAT	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80299413	TTGTGAACTCTAAAC[-/CAT]TTATACCTTTGCATA	57674
rs537907998	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80340779	GTACCCACCGCCATC[C/T]CTGGCTAATTTATTT	57674
rs537928673	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300286	TTTTTTTTTTAAGAG[A/T]CAGAGTCTGGCTCTG	57674
rs537933958	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312344	TGAGCCCAGGGGAAG[A/T]GGGGTTTTCCCTCTG	57674
rs537949021	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306544	CATGGAAAGCTCAGG[A/T]TTCTTATTCCTAAAA	57674
rs537953664	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286732	TGCTGCCTGGCAGTT[G/T]GGGGCCCTCATCACA	57674
rs537958246	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357205	TAGACGTGAGCCACC[A/G]TGCCCAGCCACCTTT	57674
rs537964439	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368735	ACCACACCTGGCCGA[C/T]GCCACTGGTTTTAAT	57674
rs537974381	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318594	TTTTTTTTTTTTTGA[G/T]ACGGGGTCTCGCTCT	57674
rs537985231	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311572	CACCTGCATCCTGGT[C/T]CCTCTTACATGCTTT	57674
rs537987485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376197	GTGGTGATTTCTCCA[C/T]ATTTACCTTGATATT	57674
rs537998030	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371356	TTTTCTTCATGTTCT[C/T]CCATATGCTGCAGCG	57674
rs538020206	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320910	GAGGCTCCCTTGGGC[C/T]CAGAAGGTCAAGGCA	57674
rs538036510	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395924	GCAGTTCCCGTTTCC[A/G]CCATGGATGCCTCAT	57674
rs538055903	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381528	CCCCGCTGAACACTC[C/T]GTTCCGTTGCCCCCA	57674
rs538068274	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390792	TCCTAGGCCGGGTGT[A/G]GAGGCTTACCCTGTA	57674
rs538099250	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365128	GGTGTCCAGCAACAG[C/T]GGCCACTCAGCCAAA	57674
rs538105617	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391172	TTGCCAATCTAAAGG[C/T]CAAAATGGTATCTCA	57674
rs538122981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366152	GCCCTGCCTTCCGCC[A/G]TGAGGCTGGCTCCCT	57674
rs538126969	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80290487	CGTGTGTGTGCGCAC[A/G]TGTGTGTGTGCGCGT	57674
rs538158296	snp	A/G	0.000200615	0.0100134	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372026	TTTCTTTTGGAAACT[A/G]TCTGAACCACATGGT	57674
rs538162005	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290220	GGGGGTGGTGTGTCA[C/T]ACGTGGACGTGCTTG	57674
rs538165078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365724	ATAGTAGGACACAGC[C/T]GGTGCCCCCCTTCCA	57674
rs538178366	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266353	TGGGAAGTCGAGGCT[G/T]CAGTAAGCCATGATT	57674
rs538186709	in-del	-/AGCT	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80330098	TTAGGTTTTCATGTC[-/AGCT]TTCGTATATATATTT	57674
rs538208177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369393	ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAAAAA	57674
rs538221058	in-del	-/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395249	GAGGCAAAAAAAAAA[-/G]AAAATGAATTTTATT	57674
rs538222030	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80275002	GTGTGTATGTGTTGG[C/G]GTATGTGAGTTGGTG	57674
rs538239558	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259479	CCAAAAAACAAACAA[A/G]CAATAAATAAAGTGC	57674
rs538240121	snp	A/G	3.30126e-05	0.00406266	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351717	AAATCAACAAAATAC[A/G]AGAAAATGAGGACCG	57674
rs538253742	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263250	CCTGTGGGGCAGGTG[C/T]TTTAGTCCCCTTAAG	57674
rs538274127	snp	C/T	0.000399281	0.0141238	synonymous-codon	RNF213	GRCh38.p7	17:80339281	GTTCAGGACGTGGAT[C/T]GCCATGGCCTACTGC	57674
rs538283329	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351558	ATCGGAACGGGTGGC[C/T]GTGAGACCGAACCAA	57674
rs538295524	snp	A/G	1.65935e-05	0.00288036	synonymous-codon	RNF213	GRCh38.p7	17:80346495	TGACGACAGCAGGCT[A/G]CTTCTGGATGAAATA	57674
rs538301502	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371604	GATAATATAACCCAC[A/G]TAAAAGCTCTTCGGG	57674
rs538334903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294058	TTTTTACTTCTGTTT[A/G]TAGGTCTTCACGTGG	57674
rs538341537	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364625	GAACAGCACTGACAG[C/T]GATCTGCGGCTGGGA	57674
rs538347159	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293683	AAAAAAATTGGCCGG[G/T]CGTCTTGGCAGCGGG	57674
rs538365713	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369826	TGTGGATAAGACTCC[C/T]GTCATCCGCTCAGTG	57674
rs538389798	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268333	CACTCCAGCCTGGGT[C/T]GACAGTGAGACCCTG	57674
rs538400825	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329017	TTAATTTCTAATTCC[A/G]TCGCAATCTCTGCCG	57674
rs538409868	snp	C/G	0.0126979	0.078662	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355476	GGGGTGACCGGGAAT[C/G]GGGGCTCACAGAGGA	57674
rs538442887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327252	CGTATAATCCTAATG[C/T]TTTGGGAGGCCAAGG	57674
rs538452108	snp	A/C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396352	ATGTGTTAACCGAGA[A/C/T]GGCCCTGAGCTATTT	57674
rs538463914	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80306633	GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG	57674
rs538479406	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354875	GACATTCATGTTGAT[A/G]ACCCTAGAAAGGGCT	57674
rs538504327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356040	GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	57674
rs538506403	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269160	TAGCCACGCTGGCAG[C/T]TGACTGGATGCTGCC	57674
rs538533953	snp	A/C	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304618	GCACTCCAGCCAAGG[A/C]AACAGAGTGAGACTC	57674
rs538543154	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374974	TCATAATTCAGATAT[A/G]CATGTGTGTTTAATA	57674
rs538549121	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355495	GCTCACAGAGGAAGA[A/T]GCGGGGTGACCGGGA	57674
rs538557990	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321783	GGCTGGAGTGCAGTG[A/G]CGTGATCTTGGCTCA	57674
rs538577327	snp	A/G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381992	CTGGCTAAGACCTGC[A/G/T]GTATTCGGGAGCGTC	57674
rs538586057	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375597	TGTAGTCCCAGCTAC[G/T]CGGGAGGCTGAGTTA	57674
rs538586962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380609	TCAATACCACACAGC[A/G]CAGCCACCTGACGCT	57674
rs538594214	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305319	AAGTAGCTGGGATTA[C/T]AGGTGTGCGCCACCA	57674
rs538606943	snp	C/T	0.000231857	0.0107645	missense	RNF213	GRCh38.p7	17:80340005	GCACTGTTGCTGCGC[C/T]GCTGCCTGACCCTGG	57674
rs538614106	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80336776	AGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC	57674
rs538642306	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326061	CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	57674
rs538670385	snp	C/T	0.00127736	0.0252398	missense	RNF213	GRCh38.p7	17:80332330	ACTATTTGTATCAGC[C/T]TTCTTACAGAAAGTT	57674
rs538708056	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80306850	GAGCGAGACTCCATC[-/T]CAAAAAAAAAAAAAA	57674
rs538719103	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354360	ACGGACTTCCCTTCC[G/T]GGGGGAGGTGGGACA	57674
rs538729090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299679	TATTAAGCCTAGTAC[C/T]CATTAGCTATTTTTC	57674
rs538749733	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80334323	AAAGTTTTCAGATGG[C/T]GCACTGTGTGGCGTT	57674
rs538763027	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80263918	CTACTGAGGCTCTGT[A/G]GCTCTGAATAGCCAT	57674
rs538763888	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356745	TTTGTGTTCGCGACA[C/G]TTTTCCTAGTTTGCT	57674
rs538793139	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80271835	TACAAAAAAAATTAG[C/T]TGGGTGTGGTGGCGC	57674
rs538801201	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319135	TTTTCATCCCATAGA[A/G]CACTGGAGCGCTGCA	57674
rs538805382	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320110	GATATGTACAGTCAT[C/G]ACCACAGTTAATGAC	57674
rs538806967	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385266	GGGCGGAGGGGAGGA[C/G]GCGCTGATGGGTGCT	57674
rs538811232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309634	TAACAAAGGCCATAG[C/T]GCCACACATCTGCCC	57674
rs538822912	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352752	CGATGGGCATAGAAT[C/T]GGGTCGTGTATAGTA	57674
rs538828287	snp	C/G	0.000231294	0.0107514	missense	RNF213	GRCh38.p7	17:80337606	CTCCGCCAGGAACTT[C/G]GAATGGCTGAAGACT	57674
rs538829411	snp	G/T	1.65064e-05	0.00287279	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389782	CACGACATGAGTGGG[G/T]GTGTGAGACCTCAGC	57674
rs538835062	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384905	GTTTTCAAGCTCCAC[A/G]CTGCATCACAGGAAA	57674
rs538844953	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80268586	CCAATTCTCCTAATA[C/T]ATCCTCTCTCATCCA	57674
rs538847958	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316619	CCTCTCCACGTTGCA[C/T]GTCCTGAGTGGGAAA	57674
rs538854802	snp	A/G	0.0111196	0.0737302	intron-variant	RNF213	GRCh38.p7	17:80297218	GCACTTTGGGAGGTC[A/G]AGGCAGGCGGATCAC	57674
rs538857886	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384494	CATTTCTCTCCATGG[A/T]CTATTATTTGCTGTC	57674
rs538861911	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320415	TGGAGTGCAATGGTG[C/T]GATCCTGGCTCACCG	57674
rs538904712	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338149	GAGTAGAGTTGGCAC[A/C]TTTGTAGGGTGCATG	57674
rs538965496	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298170	GCTGAGGGAAGCCCT[C/G]TCTCCTGCGTGAGTT	57674
rs539000371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261948	CTAGAGCCCGGGAGG[C/T]GGAGGTTGCAGTGAG	57674
rs539011828	in-del	-/TATT	0.00439032	0.0466464	intron-variant	RNF213	GRCh38.p7	17:80305039	TGAATTCTTTTTGTG[-/TATT]TATTTATTTATTTGT	57674
rs539017766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388873	GTAGAGTAAAAGCAG[A/G]TTGACATCTTGTGGG	57674
rs539019447	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80313477	GGTGATGGTGGTGGA[A/G]GTGATGGTGATGGTT	57674
rs539036380	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262424	TGGGGCTGGAGAGGG[G/T]AGGTGTGCAGGGTTG	57674
rs539053809	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394610	ATATGTTAGAGGCAG[C/T]ATCCTTAATATTCAT	57674
rs539054541	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388530	TACGCTGCAGTTTTC[C/T]GGCTGCAGATTCTGT	57674
rs539078424	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396933	GCCCCTGCTCAGGTG[C/T]TCCACAGCCCATAAA	57674
rs539079276	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395115	TTTTCCTTTGGCCTG[C/G]GAATTTTTCCCATTT	57674
rs539081098	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80273613	TGGGGCCTCCACCGT[-/C]TTTTTTTTTTTTTTT	57674
rs539093916	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359429	CTCTAGAAGCTGAGG[C/T]GGGAGGATTGCTTGA	57674
rs539118505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348756	CCTCGCCGATGGGGA[A/G]GAATGGCCGGGAAGG	57674
rs539148237	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80323983	ATTGTGTGTGCGTGT[A/G]TGTGTGTGTGTGCAT	57674
rs539154071	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80288888	AAAGCTCTGGCCTTC[A/G]GGGTGCTCACATTCC	57674
rs539180471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389541	GACACACCAGGGACA[A/G]TAGAGACAGACACGC	57674
rs539183409	snp	C/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80315306	GTGGTGGAGGTAATG[C/G]AGGTGATGGTGGTGG	57674
rs539187745	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384484	ATTGTCTAAACATTT[A/C]TCTCCATGGACTATT	57674
rs539192730	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373984	CTCCAGCGCCTGGGC[A/G]ATAGAGCGAGACTCC	57674
rs539207563	in-del	-/TTTT			intron-variant	RNF213	GRCh38.p7	17:80273633	TTTTTTTTTTTTTTT[-/TTTT]GAGACAGAGTTTCGC	57674
rs539235944	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272929	GTTTTAGAGGTGCCC[G/T]AGGTGCGCTGACATC	57674
rs539251144	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397753	TAACTCGTGTCTGAG[A/G]GGTTTTCTCTGCAGC	57674
rs539267283	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393105	ACCTCAGCCTCCTGA[C/G]TAGCTTCGGACTATA	57674
rs539270111	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260304	GCGCCGGGGCGGGGG[A/G]CGCGCCTGTCCCGCC	57674
rs539272294	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398965	ATATCCCGAAAGCAC[G/T]GAGGCCTTCCCATCA	57674
rs539278764	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291509	ATTTCAGGCATGGGC[C/T]ACTGAACCCAGCCTT	57674
rs539299036	in-del	-/AT	0.00120168	0.0244826	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398797	AAAAGAAAAAAAGAG[-/AT]ATATATATACAAGTA	57674
rs539299818	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367497	ATATCTTAGTGAGAG[C/G]GGAGGAGACCTTAAA	57674
rs539303146	snp	A/G	1.64789e-05	0.0028704	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393459	TGTCTCAGTGTGGAA[A/G]ACAGCTGCTGTGCTG	57674
rs539312403	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317577	TGTGTTTACTTGGCC[C/T]GCCGTGCTCAACCCC	57674
rs539321115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368595	GCACCACCATGCCCG[A/G]CTAATTTTTGTATTT	57674
rs539327445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292309	TTGACCTCAGGTGAT[C/T]TGCCCTCCTCGACCT	57674
rs539361865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362836	TGGGTTATTGAGCAG[C/T]CATTAAAACCATGTT	57674
rs539365242	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367997	CATCTGCCTGGGAGA[C/T]GCAAAGGACCCCGTC	57674
rs539398961	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324653	GGCAGCTTTTTAAAA[G/T]AATTATGGTTTAGGA	57674
rs539409121	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307542	TAATTTTTGTGTGTT[G/T]GTTTGTTTGTTTGTT	57674
rs539409630	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372184	TATACATACAAAACA[A/G]AACAGCCTAGGAGAA	57674
rs539434987	snp	C/G	0.000263604	0.0114775	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353687	TTCTGGTTCTTGGGA[C/G]CTCCCCTTGTGCTGC	57674
rs539443987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342484	GAGAAGTAACTTCTA[A/G]TGGATCTTTATAGAT	57674
rs539448154	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272141	ACACAAAAATTAGCC[A/G]GGTGTGGTGGCATGC	57674
rs539453309	snp	A/G			intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360447	TGGCAGCAGGAGCCT[A/G]TGAGATGGTTTTTAG	57674
rs539458718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271642	CTTGAAGGGTGTTTT[C/T]GTCCATTTTCTGTTG	57674
rs539466554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261642	TGTCAGAGAAAAGAC[A/G]GGAAGCGGATTGAAT	57674
rs539468166	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281815	ATGAAACGGCGTGGC[A/G]TTGGTACATAACCCA	57674
rs539504584	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80278244	CTCCCGGCGATGCCC[A/G]GTGTGGTGTGGAAGG	57674
rs539537225	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80297064	GCAATGTACAGAGTT[A/G]GTGCCGGGGCTTAAA	57674
rs539543962	in-del	-/CGGCGG	0.249886	0.25	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260812	CGGGCAGGGCGGGGC[-/CGGCGG]CGGCGGCGGCGGGCA	57674
rs539596025	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80266525	TCATTGTTTTGAGAC[A/C]GAGTCTTGCTCTGTC	57674
rs539604930	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323941	TCTTGTATCCTGCAA[A/C]ATTGCTGAGCTCATT	57674
rs539626648	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330757	TCTCTTGGCTGCTGG[C/G]GTGAAGAAGGGGGTC	57674
rs539629288	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80281564	ACCCCCCAAGACAAA[C/T]GCCCCACTCACACCA	57674
rs539649604	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357515	TGTTTAGTTTGATCT[-/G]GGACAAATTCATTTT	57674
rs539652546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322704	GAAGGCATGAGCCAC[C/T]GCACCTGGCCTCTTT	57674
rs539655112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387034	ACCTGCAGCTCCCGA[A/G]GCCACCACGCCACCT	57674
rs539664198	snp	G/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80330030	CTCTCGGATTTTCTA[G/T]CTCTGTTTTTTGCTC	57674
rs539664375	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362294	TTCAGTACATAAAAA[A/G]GGAGAGTGACAAATT	57674
rs539675466	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351864	ATTTATTTGTATCTA[A/T]TTATTTTTTGAGATG	57674
rs539683180	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349366	TGACCTTTGGGACAG[A/G]AGAATTGCTGACATC	57674
rs539683660	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80280910	AGAGGCGCGACCTGG[A/G]GATGCGCACGGAGCA	57674
rs539687544	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357131	CATGTTGGCCAGGCT[A/G]GTCTCGAACTCCTGA	57674
rs539692356	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80286673	TCTTCCCAGGTATGT[A/G]GGTGCAGGAGGTGGG	57674
rs539706707	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368897	TCTTTCCTTCCCCTT[-/C]CCCCCCTTCTCAGGC	57674
rs539711511	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299293	CATTTGGTTGGTTGT[A/G]CAGTTTCGTTTTTTC	57674
rs539713683	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358179	AGTGTGGTAAATAGT[A/G]GACTAGTTGTTTTGT	57674
rs539720344	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80262956	TGGGTGGGCCAGTGT[C/G]CCCTGAGGCTTCTTA	57674
rs539737220	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287503	GGAGACCTTGTCTCA[A/G]ATAAATAAATAAATA	57674
rs539741612	snp	G/T	0.000136263	0.00825306	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382965	TAACCTACACATTTG[G/T]AGTTTTTTTGTAGGG	57674
rs539742741	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377555	GATAAAATTAATAAA[A/G]TTAGACTCAGACATT	57674
rs539753720	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357836	AAATAAAATTTAAAA[A/G]TTAGCTGGGCATGGT	57674
rs539830271	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386210	ATTCTGTGAGGAGTT[A/G]GAACTCCTCTCTGCT	57674
rs539838628	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80336014	AAAGATTAGGTGTTC[C/T]GGACTCTTACTGAAA	57674
rs539853523	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341998	GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	57674
rs539894412	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280579	GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	57674
rs539954778	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280181	TGGACTTAGCCAGAC[C/G]TAAGGCACAGTGTGG	57674
rs539959892	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80350648	CATTTCTAAAAAAAT[A/G]AAATAATTAGCCTTC	57674
rs539965585	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259869	AGGATGTTGGACTAA[C/T]TGTTGGCGACCCCCC	57674
rs540004284	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80339539	GCCCCCGAGTGATGC[C/T]GCCCTAACGATGCTA	57674
rs540009692	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318534	TTAAGGCCTGAGGCT[C/T]AAGGAAAATTAGTTT	57674
rs540011892	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311685	CTCTCTCCCACTCTC[A/G]GGCAGCCCCGCCCAG	57674
rs540012253	snp	C/T	0.00107103	0.0231163	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364417	TGAGTGAGTGAGTGG[C/T]GCCCTCTTTTGACAG	57674
rs540021736	snp	C/G	0.000214535	0.0103548	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372750	GCAAGTCTTCTCTGC[C/G]TTGCTTTCCTTTGGG	57674
rs540028367	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392379	AATACAAGGTTTTTT[A/G]AATGGTGAGGCCTTG	57674
rs540042327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264387	GAGAGACAGGAGCGG[A/G]GCAGTGTCAGGCGGG	57674
rs540052248	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80326839	TTCCAAGTTTTTGCA[A/G]TGATTAGTAAAGCTA	57674
rs540070804	snp	G/T	1.7263e-05	0.00293789	synonymous-codon	RNF213	GRCh38.p7	17:80340316	CGTGTTCAATGACCG[G/T]CTGTGTGTTGGGATC	57674
rs540073006	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80312894	CTGTGGTCCCTCCAT[C/T]GTAGCCACTCCTTGA	57674
rs540094757	snp	C/T	0.00116223	0.0240783	missense	RNF213	GRCh38.p7	17:80347168	GAAACGGTGTGTAAG[C/T]GCCAGGACAAGGAAT	57674
rs540121105	snp	A/G	0.000399281	0.0141238	intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360348	GTTTGTGCAGTAAGC[A/G]TCCAATTTACGTCAC	57674
rs540150231	in-del	-/TT	0.0722614	0.17581	intron-variant	RNF213	GRCh38.p7	17:80275963	ACCATGCCTGGCCAG[-/TT]TTTTTTTTTTTCTTT	57674
rs540150868	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366883	ATCATGCCTGCCCAT[A/C]AAATTCCATTAGTAC	57674
rs540213726	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390909	TCTACTAAAAATACA[A/T]AAATTAGCCAGGCAT	57674
rs540218037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317489	GACAGAGAAGAACAA[A/G]GGCCCAGGATCTCAC	57674
rs540240921	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317096	TCCCGCGCTCTCTGT[A/G]TTGCCGTAATGCTCT	57674
rs540250099	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391311	CGTGTCTCACTCCCA[C/G]CCAAGCTGGAGTGCA	57674
rs540253159	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269479	CCATTCATCTATTCT[A/G]TCTATCCATCCATCC	57674
rs540277501	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309856	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGTCT	57674
rs540300391	snp	A/G	0.000114659	0.00757076	missense	RNF213	GRCh38.p7	17:80339486	AACTTCTACACGGCA[A/G]AGCAGCTGGTTTACC	57674
rs540378106	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317797	GTGGGTCCCTTGCCT[G/T]GTTGCCTAGGGTGGC	57674
rs540382915	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352065	TCACCACGTTGGCCT[A/C]GATGGTCTCAATCCG	57674
rs540396094	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80299811	CAAGTGAGAACCTGC[A/G]GTATTTGGTTCTCGT	57674
rs540406834	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394736	TGAGCAGCGCCGGCA[A/G]GAGGCACGGAAGGAA	57674
rs540432865	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287088	AAACCAGGCCAGGCA[C/T]GGTGGCTCACGCGTG	57674
rs540433526	snp	A/G			missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351728	ATACGAGAAAATGAG[A/G]ACCGTATCTTCGTCT	57674
rs540481629	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327472	GGTGACAGAGAGAGA[A/C]CCTGTCAAAAAAAAA	57674
rs540492292	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80269332	ATATTAACCATCACA[-/C]CCGTCTATCCATCCC	57674
rs540514199	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80289997	CTTAGGAGGTGGAGG[A/G]GGGTGGGCACCTGTG	57674
rs540539813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294282	CAGGGGCTGTGTCCC[A/G]TTCCTAGTACAGAGG	57674
rs540540740	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364844	TGTGAAACCTTCGGC[A/C]GGGATTACCTGGCCT	57674
rs540592541	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310206	CACCCACTTGAGTTC[A/G]TGAGTTTCAGTTTGA	57674
rs540593268	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298247	GGTGCTTGCTTCCTG[C/T]TGGGACTCCAGACTC	57674
rs540604793	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380699	GGAACATGGTCCAGG[A/C]TTTGTGGAACAGCAA	57674
rs540618390	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384981	CTCAAAGTCTGTAAC[C/G]CCAATAACATTTTTT	57674
rs540628297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368235	AAACTCTATTAACCT[C/T]CATTTGGTAGAAAAC	57674
rs540631690	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385423	GCACCTCAGACATGC[C/T]TGTGACTGCACAAAG	57674
rs540642819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380347	ATCTCCAGAAACTGT[C/T]ACAGTGTCCTCCATC	57674
rs540665093	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332044	AGACACTCACAAGAC[C/T]TCAGCAGTAAAAGAT	57674
rs540666647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349973	GTGGCTTCTGCGTGG[C/T]GATGGTACCCGCGCC	57674
rs540697153	snp	A/C	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80269805	CTACCTGTCTACCTA[A/C]CTACCTACATATTCT	57674
rs540708682	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299144	TGTGTTATTTATTCT[A/G]GTTTACAACCTGATT	57674
rs540730325	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375688	AGCCTGGGTGACAGA[G/T]CAAGACTCCATCTCA	57674
rs540760117	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288533	GGATGCCAGCCCACC[C/T]TGTCCCTCGGCTTGT	57674
rs540761806	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304833	TCCCGAACTCAGCTT[C/T]CCCAGCTGAAACTCC	57674
rs540767389	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375252	TTTCAGGAACTTTGT[A/G]GCCCAAAAGTTGCTC	57674
rs540768524	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394360	AGTCTCAGTGTGCTC[G/T]CGCATGTATGAATAT	57674
rs540788895	snp	A/C	1.71914e-05	0.0029318	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363761	GCAAGGCAGCGGGAG[A/C]CTGGCCCAGGCTGTC	57674
rs540826147	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80290496	GCGCACGTGTGTGTG[C/T]GCGCGTGTGTGCATG	57674
rs540849752	snp	C/T	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80288972	GGGAGAGAGGGCACC[C/T]AGGTGGGCCCCGAGG	57674
rs540873689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359091	TCTGTGCTCCCTCCC[C/T]GTCCCTCATTCCCTG	57674
rs540874953	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277972	ACAGAGAGGGGCCCG[C/T]GCCTGTCCCTTGGCA	57674
rs540925952	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374163	GAGTTGACATGACTT[C/G]AGCCACCCGGCCTCA	57674
rs540934888	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354547	GGAAGCCTGCAACCA[A/G]GACGCTCTCCAGGAG	57674
rs540937209	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284130	TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA	57674
rs540941842	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80268234	TGGCTATTGTGAATC[A/G]TGCTACAGTGAGCAT	57674
rs540981569	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357947	GATCTATGATTGTGT[A/C]ACTACACCGCAGTTG	57674
rs540998014	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80318618	TCGCTCTATCGCCCA[C/G]GCTGGAGTGCAGTGG	57674
rs541030703	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261619	CAGTGTCTGTGCTTG[C/G]GAAAAAATGTCAGAG	57674
rs541031539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268829	TGTATTATGGAGAAT[C/T]GGCTCACACAATCAC	57674
rs541059478	snp	A/G	0.000230282	0.0107279	intron-variant	RNF213	GRCh38.p7	17:80337750	TCCCCAGCCCTCGGC[A/G]CAGCTGCGGCCCTTC	57674
rs541063730	snp	C/T			intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319363	CTCACAGCTGTGTTC[C/T]GCCATGACCCAGCTA	57674
rs541065668	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382117	TCCACACAGAGCGTG[C/T]GTGTCAAAGGATCAA	57674
rs541085247	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80324272	TTCCTTTTTGTTCCT[A/C]ATTTGTTGAATGCTT	57674
rs541087490	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80282865	ACCACGCCTGGCTAA[A/T]TTTTGTATTTTTAGT	57674
rs541101191	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287591	GGCCGTGACCGTGCC[G/T]AGTGTGGCGAGCGCT	57674
rs541110402	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358857	GAGGTTGCAGTGAGC[C/T]GAGATGGCGCCACTG	57674
rs541146727	snp	C/G	1.64814e-05	0.00287061	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358321	GGTCCAAGGTGCTGT[C/G]ACCCCTCTGCTGGCG	57674
rs541149137	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282351	GTGGCTGCAGAGGGC[C/T]GACTGTATACCAGCT	57674
rs541169857	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283131	ATGGTTATGTAGTTC[A/G]AGATTCTGGGTCAAA	57674
rs541205741	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383127	GAAAGGAAGGGTCCC[A/G]GCGTCTGCTGAATGC	57674
rs541215578	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260052	AAACGGAGGTCCCTG[A/G]TCACACCATGAGCCT	57674
rs541232107	snp	C/G	7.56001e-05	0.00614771	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372774	CTTTGGGTTTAAAGA[C/G]TCCGTTATTTAGAAA	57674
rs541233216	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80316249	GGAGCGAGACCCTGT[C/G]TCTTAAAATATTTTT	57674
rs541235763	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80266887	CTGAGATAGGCTGAT[A/G]GCTAGGCCTCTTGCA	57674
rs541237159	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80313716	ATGGTGGTGATGGAG[A/G]TGGTGGTGGTGGAGG	57674
rs541263205	snp	A/G	0.0162398	0.0886349	intron-variant	RNF213	GRCh38.p7	17:80342750	ATATATATATTGTAT[A/G]TATATATATATTATA	57674
rs541304938	in-del	-/AAAA	0.00320898	0.0399273	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354821	ATACTAAAAACTTAA[-/AAAA]AGTAAAACATCTGTT	57674
rs541306067	in-del	-/TG	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80285843	GCCCAGCTAATTTTT[-/TG]TGTTTTTAGTAGAGA	57674
rs541310758	snp	A/G			intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360405	GGAGTGAGAGGCCCC[A/G]GCGGGACCAGAAACC	57674
rs541317259	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362489	ACTATTAATAGCAAA[G/T]CAACACAACAGTTTT	57674
rs541326791	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80349037	TACAAAGGAGAGGAG[A/C]AGATGGAACCGAGAG	57674
rs541332436	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80297230	GTCGAGGCAGGCGGA[G/T]CACAAGGTCAGGAGT	57674
rs541353456	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80261055	CAAGTTTCGGTTTCG[C/T]CGCCGGGGTGCCCGG	57674
rs541407396	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371079	AGCCCAGTGAACCAA[A/T]ATTTTCCAAATGACC	57674
rs541414394	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393222	CTGACCTCCACTGAC[C/T]CACCCACCTCAGCCT	57674
rs541433044	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318612	GGGGTCTCGCTCTAT[C/T]GCCCAGGCTGGAGTG	57674
rs541451082	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393574	CGGCGTGGACTTGAT[C/G]ATGGACTGGTGCCTT	57674
rs541469884	snp	C/T	6.64507e-05	0.00576376	synonymous-codon	RNF213	GRCh38.p7	17:80346903	CTCACCCAAAATGCC[C/T]CTGAAGACTCTGCAC	57674
rs541486971	in-del	-/TTTA	0.00756208	0.0610234	intron-variant	RNF213	GRCh38.p7	17:80276065	GGAACATAGACTTTA[-/TTTA]TTTATTTATTTATTT	57674
rs541494608	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342204	GGGCAATGGGCTATT[C/G]CACCTAGCTCGGGTG	57674
rs541497212	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80296339	TACCCTGCTTTTTGA[A/G]GCTTCGTGTGGTATC	57674
rs541501583	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352460	GGGGAGGGAGAGTGG[C/T]GGGGGTCGGACTATC	57674
rs541531635	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393290	GCTGGGCTTACACAC[A/G]TGAGCCACCATGCTG	57674
rs541534040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271793	ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCGTC	57674
rs541556671	in-del	-/A	0.297382	0.245469	intron-variant	RNF213	GRCh38.p7	17:80338958	TCTCAAAAAAAAATT[-/A]AAAAAAAAAAAAAAA	57674
rs541581943	snp	A/G	6.59805e-05	0.00574333	intron-variant, missense	RNF213	GRCh38.p7	17:80319415	GGTCTCAGCTCCTCC[A/G]CTAACTCAGAGATTG	57674
rs541591604	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307267	CTTCCTCTGACCCCT[A/G]TAATTGGCCGTGACC	57674
rs541606208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296821	TGAGTAGCTGGGACT[A/G]CAGATACACACCACC	57674
rs541608106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302314	AATAAATGTTTGAGA[C/T]AGATATGCTAATTAC	57674
rs541613352	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80329703	AGACACGGTGGTGCA[C/T]GCCTGTATTCCCAAC	57674
rs541641720	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80322003	TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC	57674
rs541646621	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378073	GACCTCGAGTCCCTG[C/G]ATGCCAGGAGCACCC	57674
rs541656510	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360636	CCTGGAGCATCCCCT[A/G]CTCCCAGGTGCCCCA	57674
rs541667393	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396481	CCACCCAAGTCTAGC[C/T]ATGCACACAGGCACT	57674
rs541689301	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80290509	TGTGCGCGTGTGTGC[A/G]TGCACATGGCAGGTG	57674
rs541709534	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392548	TTGAACCCAGGATGC[C/T]AGTCCCAGTTCAGGA	57674
rs541753836	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297207	CTGTAATCCCAGCAC[G/T]TTGGGAGGTCGAGGC	57674
rs541784883	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398760	GAAAGTCAAAGAGAA[A/G]GAGACAGAAAATCAA	57674
rs541857606	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276324	AGGCTGGTCTTGAAC[G/T]CCTGACTTCAGGTGC	57674
rs541858298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382064	TTCCGAAGTCAGCCC[C/T]GTAGGTCATTCCCCT	57674
rs541884322	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80317570	GGGATGCTGTGTTTA[C/T]TTGGCCCGCCGTGCT	57674
rs541906615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372304	ATGTAAATAAATTAG[A/G]TAATTTTTTTTCCTC	57674
rs541918121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335395	GTCTGGGGGCCACCA[C/T]CTGCTGGATCTCAGG	57674
rs541940369	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80261923	TTGGGAGACTGAGGC[A/G]GGAGAATCGCTAGAG	57674
rs541954747	snp	C/T	0.000399281	0.0141238	synonymous-codon	RNF213	GRCh38.p7	17:80295685	CCTGATTGTCCTTTT[C/T]GTAGTGGAAAAAATT	57674
rs541959503	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396687	TACCATTACGAATCC[C/T]GTTTCCAGCTGGAAA	57674
rs541985317	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371434	AGGGCCAGCACAGGA[A/G]TGGAAGACCAAACCA	57674
rs541990118	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299657	ACAGATTATTTCATC[A/G]TCCAAATATTAAGCC	57674
rs541994399	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381144	CATCTTCATGTTTCC[C/T]CCTGTGGCGTATGAT	57674
rs542001313	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361183	GGGGCTAGCTTGGCT[G/T]TTTCTGACCTAAATT	57674
rs542030217	snp	A/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80324678	TTAGGAACATAAAAT[A/G]TATGCTATATTAAGG	57674
rs542034487	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386532	CTTCCCTAACAGACA[C/G/T]TCACTCCTTCAGCCG	57674
rs542064594	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259293	GCCAACATGGAGAAA[C/T]CCCGTCTCTACTAAA	57674
rs542081138	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285918	TGACCTCCAGTGATC[C/T]GCCTGCCTCGGCCTC	57674
rs542086655	snp	A/G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351958	CTCCTGGGTTCAAGC[A/G/T]ATTCTCCTGCCTCAG	57674
rs542123429	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356825	TAAAATTCTTGCCAG[A/G]TTCCTCTGTACTATA	57674
rs542124733	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321915	ATTTTTGGTAGAGAC[A/G]GGGTTTTGCCGTGTG	57674
rs542128731	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275227	TGTGCTTGTGTCATT[A/C]CCTTGGAGAATAATC	57674
rs542134963	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387904	CATATCTACTGTACT[A/T]ATGTACGGTACCACC	57674
rs542161235	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80305545	CCATAGGAGCATGCC[C/G]AGAATGGCCAGCAGT	57674
rs542168942	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80286334	CTGAGCATGGGTTTC[C/T]TCTGAATTTAAAAAG	57674
rs542188417	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311319	TGACGGACACTTGGA[A/G]AACAAGGTGCCCGTG	57674
rs542198349	snp	G/T	1.64928e-05	0.00287161	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375871	CACCCCACGCCAGAG[G/T]TGAGTAACCGCCTGC	57674
rs542207029	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334847	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	57674
rs542225557	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389302	GGTGGGGATCCAAAC[A/G]TGCAGCTGAATGTGT	57674
rs542235974	snp	G/T	0.0103295	0.0711199	intron-variant	RNF213	GRCh38.p7	17:80265052	TTTGTTTGTTTTTTT[G/T]TTTTTTTTTAGAGGG	57674
rs542269694	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328252	GCGGGGAAGGTGCGG[C/T]GCTTTCAAAGCATTG	57674
rs542271359	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285233	ACATCTGCTGTCTCC[A/G]CTTTAAAGATGGGGA	57674
rs542287004	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388066	CCGGGTTCACTCATG[C/T]CATTCTCCTGCCGCA	57674
rs542301004	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80334754	GCCTCAGCCTCCCGA[C/G]TAGCTGGGACTACAG	57674
rs542304501	snp	C/T	0.0298908	0.118541	intron-variant	RNF213	GRCh38.p7	17:80290412	GTGTGCTTGTGTGTG[C/T]GCGTGTGTGCGAGTG	57674
rs542318594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80295148	CTCCTACCACTGTCT[C/T]TTGGGATTTCTCTGC	57674
rs542326780	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365459	CCCTTCATTGTCCCT[A/G]ATGTTCAGCTTCCAC	57674
rs542374260	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355219	CAGCGGACTCCTCCA[C/T]GAGTCCCCTTCCAGG	57674
rs542377924	snp	A/G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80310678	CTGCCTCAGCCTCCC[A/G/T]AGTAGCTGGGATTAC	57674
rs542392405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274549	ACTCCATGGTTGGGC[C/T]ATGGTGGGAAGTGAT	57674
rs542393002	in-del	-/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80316259	CTGTCTCTTAAAATA[-/T]TTTTTTTTACAGTGC	57674
rs542406000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262885	CACCAGTCAGCTGCC[A/G]CTCCAGCCACTGCCC	57674
rs542407858	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269763	TCTTATCTATCCATC[C/T]GTCCATCCATCCATG	57674
rs542425565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369071	AAGACTAGCTCTAAC[A/G]GGTGAGAGGAGTGAC	57674
rs542455084	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378028	GGCGTGGGCTGTCCT[G/T]TGCACTGCAGGCTGT	57674
rs542458269	snp	C/T	0.000100949	0.00710382	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374693	GATGGACCACTGATG[C/T]AGCCCATCACGTGAC	57674
rs542480315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270358	TGAGCCAGGCTGGCC[A/G]TCTGGAGGACAGATT	57674
rs542492632	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80338720	TTGGGAGGCCGAGGC[A/G]GGCCTATCACTTGAG	57674
rs542502765	in-del	-/ACAT	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377582	CATTTTTCACTGACA[-/ACAT]ACATTTATTAAGCTT	57674
rs542506166	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364351	GGGTCCCGCATCTCT[C/T]CTCCCGTCTCCCTCC	57674
rs542513870	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340445	GAAGCCTGTCTGCAG[G/T]TGGAGAAACCGAGGC	57674
rs542544842	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263331	GCCGTGGGACCCTGC[C/T]GAACAGCACGTGGCT	57674
rs542556066	snp	A/C/G			intron-variant	RNF213	GRCh38.p7	17:80337747	CGGTCCCCAGCCCTC[A/C/G]GCGCAGCTGCGGCCC	57674
rs542564856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293176	GATCCTCCCCCTCAG[C/T]CCCCCCAAGTAGCTG	57674
rs542617219	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320116	TACAGTCATCACCAC[A/T]GTTAATGACAGAGCA	57674
rs542619576	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395941	CATGGATGCCTCATC[A/C]CCAACCCTGACCTTC	57674
rs542624097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309261	AAACAGACTGATTCC[C/T]GGGTGCTGGGATGAG	57674
rs542624880	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356893	AAAAGAGAGGCTTCG[C/T]TTTTCCCCCAACATT	57674
rs542628768	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320611	GTCAGGCTGGTCTCG[A/T]ACTCCCGACCTCAGG	57674
rs542658772	snp	A/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80279033	GGAAGGCTGCCCAGG[A/T]TGGGCGTTTTCGGGT	57674
rs542660122	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80349165	GAGTGGACATTGCTT[C/T]ATCATGACAGATACC	57674
rs542661206	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316205	TGCAGTGAGCTATGA[C/T]TGTGCCACTGCACTC	57674
rs542723600	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80349596	CCTGTAGGGCCTCTC[A/G]GCCCCAGCGCTGCCG	57674
rs542786177	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321161	GGACCCAGAGTCTAA[A/C]CACAAAATTCACTTG	57674
rs542805548	snp	A/G	0.000455944	0.0150919	missense	RNF213	GRCh38.p7	17:80339366	GAGCTTAAAGAAGGT[A/G]GAGATGTCACTGAGC	57674
rs542814279	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270106	CCTCTGCGTGAATGT[A/G]TGCGCACACACACAC	57674
rs542814928	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304743	TCCAGTTTACCATGT[C/T]AACTCCTTTTCAAGG	57674
rs542815062	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298735	TTTGGGAGGCTGAGA[C/T]GGGTGGATCACCTGA	57674
rs542829497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324945	GATTTCAGAAATGCT[A/G]TCGAGTAGGTAATTT	57674
rs542845551	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380636	CGCTGAGAATGCGGT[A/C]GGGTCTGGTCCACCG	57674
rs542867046	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80333355	GTGAGCCACCGTGCC[C/T]GGCTGAGTCTTCTGC	57674
rs542885420	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392988	TGTTATATGGGAGCC[-/T]TTTTTTTTTGAGACA	57674
rs542934163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369476	GGAAACACCATCCAC[C/T]TGTCTTCTGTTTCTC	57674
rs542956193	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319829	CCACATGAGGAAGCT[C/G]CCTGCTGGCCACGGC	57674
rs542967489	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358779	CTGGGCGTGGTGGCG[C/T]GTGCCTGTATTCCCA	57674
rs542973358	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80316714	CAAGGTGCCATGATG[A/C]CTGCAACTTACTTTC	57674
rs542991655	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80279170	CCCACATCCTTCCAC[C/T]TGCCTTTTTACTCCG	57674
rs543018939	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373435	CTTGTCTGTCTGGTC[C/T]TTTGTCTCTGTGCTT	57674
rs543021338	snp	C/T	3.31214e-05	0.00406935	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379752	TCCTAAGTACTCAAA[C/T]TTTGGGGTGTTGGGC	57674
rs543041102	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80337364	AGGCACTGGAGGAAA[C/T]GTGGAACAGCGAGTA	57674
rs543055506	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378821	GTATATTGTGGCACA[A/G]TATCTGATTTTGAAA	57674
rs543056198	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384529	AAGGATGAAGACGAG[C/T]TGGAAACTTCTGTTG	57674
rs543077298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273776	AGGCATGCACCACCA[C/T]GACCAGCTAATTTTT	57674
rs543078310	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80310011	CGCCTGCCTTGGCCT[C/T]CAAAGTGCTGGGATT	57674
rs543104351	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331516	GCCTCAGCCTCCTGA[G/T]TAGCTGGGATTACAG	57674
rs543121184	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261554	GCCCTTCCCTGCCCC[C/G]ACCTTGTTGACTTTG	57674
rs543136863	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80309692	ATGGCAGGATGACCC[A/G]GCTCCTCCGTCCCAA	57674
rs543158744	snp	A/G	1.69003e-05	0.00290687	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358517	CTGGGGAGAGAAACT[A/G]TCAGAACACAGCAGG	57674
rs543180872	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393736	TTTATGAGTACTGTT[A/C]ATTGAGAGATGACAA	57674
rs543181688	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380225	CACAATCCCATGCTG[A/C]GATGAATGTGGTTCT	57674
rs543184976	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319564	GGAATCACGGCCGTG[C/T]GCGTGTGGCACAAGT	57674
rs543189611	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383318	CCAGCAAGTGCAGGC[A/C]GTGTTTTTCTCTCCA	57674
rs543228245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388362	TAGCGCCTCCTGTGG[C/T]GAAGCAGGCCACGAT	57674
rs543243858	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80292404	GAAAGGAGAGAAAAC[A/G]AAGCCAGAAGAAGGG	57674
rs543249524	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80265459	CCTAATTCACCACTT[G/T]TAAGAGGCCAGGAAT	57674
rs543251194	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262024	AACAAAAAATGCTTT[C/T]TGGAGGATTTTTCGA	57674
rs543257830	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80318869	TGAGCCACCGCGCCC[A/G]GCCTATATGTAACTG	57674
rs543281393	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359034	GACACGGAGACAGTG[C/T]GCTGCGAACAGCCCC	57674
rs543298779	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80282284	TGTTATTGTTGTCTC[A/G]TTATTTTCTGTTTTC	57674
rs543300386	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80283501	CAGCCCCGTGTTGTG[A/G]GCAGAGGGAGTGAGG	57674
rs543303325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308360	CAGTCCCCTCCATCA[A/G]CTCTCCTCTTAAGCT	57674
rs543303671	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80269409	TCTGTCCTATCATCT[A/G]TCCATCCATCCATCC	57674
rs543339016	snp	A/C			missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288686	AGGGGCCGGGAAGGA[A/C]ATGAAAGAGAAGACC	57674
rs543340295	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307866	TCTGTTTTTTTTTTT[G/T]TTTTTTTTTTAAAGG	57674
rs543341775	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259167	AAGATGCCCAACTAG[C/T]GTTCTAAAGTGTCAC	57674
rs543353070	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394729	CACACCTTGAGCAGC[A/G]CCGGCAGGAGGCACG	57674
rs543372723	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80275028	TGGTGTGTGAGTGGG[-/GT]GTGTGTGTGTTGGGG	57674
rs543376078	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297339	CCTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGG	57674
rs543397962	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319544	ATCCTGCATGTGTTC[C/T]ATATGGAATCACGGC	57674
rs543424245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268205	TTGTTGGATAGTTGG[C/T]GGATTCCATATCTTG	57674
rs543462087	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259921	CTGGGGTTCCGCGCC[A/G]GGAATTGTTTCAGGA	57674
rs543462451	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398579	CGTACACAGACACTT[C/G]GTTACAGCTGGTTTT	57674
rs543467522	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343427	TTCCTTGTTTCCACA[C/T]GCACAGTCCTGTGAA	57674
rs543533586	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287108	GCTCACGCGTGTAAT[C/T]CCACACTTTGGGAGG	57674
rs543534712	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374035	AAAAAGAGGCTTCAA[A/G]GCCTCTCAGTGGTCC	57674
rs543557197	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262267	ACTCTGAAGGAGAGA[G/T]AATTTTAGTCTCTGG	57674
rs543565196	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329770	TGGGAAGTCGAGGCT[A/G]CAGTGAGCCGAAATC	57674
rs543577224	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371784	CACACACACACACAG[A/G]ACAGACGACCGATAG	57674
rs543589479	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362815	AATTAAAGTATGGCC[A/G]TATGATGGGTTATTG	57674
rs543591774	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266081	AGATTATGCATTTCA[C/T]GTTGCAGCTGGTAGA	57674
rs543606482	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312532	ACCTCCGGGTCAGGA[A/G]CCTGGCTGTGGTCTG	57674
rs543620057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377645	AGCGTGGGATGCTCT[A/G]GACAGTCATTCTCAT	57674
rs543634723	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80340970	CCAGTACACCCAGCT[A/C]ATTTTTTTATTTTTA	57674
rs543645170	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80342065	AGCCTCCCAAAGTGC[A/T]GGGATTACAGGCCTG	57674
rs543647268	in-del	-/TTTA	0.000801442	0.020002	intron-variant	RNF213	GRCh38.p7	17:80276062	CAAAGGAACATAGAC[-/TTTA]TTTATTTATTTATTT	57674
rs543648652	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80277078	AGCAAACAAACCAAA[A/C]AAAAAACAAAAAAAG	57674
rs543652108	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80271249	TCTGGCTGTGATGTT[C/T]CATGTGTGTCTTATG	57674
rs543656236	in-del	-/TGTTAC	0.00336816	0.0408991	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385011	TAGGTAAATAAAAAT[-/TGTTAC]TGGGTGGTCTTCCCT	57674
rs543656835	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277869	AGAAGCTGAGACAGC[C/G]AGCTGCGTGGCCAGC	57674
rs543675004	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80266782	GCTGGGATTACAGGT[A/G]TGAGCCACCCACCGC	57674
rs543675440	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80342862	CCAGGCTGGAGTGTA[A/G]TGGTGCAATCTCAGC	57674
rs543700910	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80318720	CTGGGACTACAGGCG[A/C]CCGCCACCGCGCCCA	57674
rs543706430	snp	A/C/G	3.3004e-05	0.00406216	synonymous-codon, missense	RNF213	GRCh38.p7	17:80290727	GAGCTGCACTACACC[A/C/G]GGTGAGCGTGTCTGT	57674
rs543708939	snp	C/T	0.000121029	0.00777816	intron-variant	RNF213	GRCh38.p7	17:80336118	CGAGTCTTGTGCTAT[C/T]GTGGAATAGTCCCAC	57674
rs543709812	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389741	GAGAAGAATGCCTGT[A/G]TGGAGAGCACTCAGG	57674
rs543722856	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360828	TTTACTTATCGTACC[A/G]TTTGGAAGACTCAGG	57674
rs543726928	snp	A/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360815	AGTCTTTTCCACGTT[A/T]ACTTATCGTACCATT	57674
rs543727422	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80313587	GTCATGGAGGTGGTG[A/G]AGGTGATGGTGGTGG	57674
rs543752254	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80348074	TTGACGGAGGAACTT[C/T]ACCAGAAGGTGTCTG	57674
rs543759568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296657	AGCATGTCTTATCAC[A/G]ACATCTGCCTCTCAG	57674
rs543819325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323277	AGTACCACACTGTTT[A/G]GACTACCATTGCTTT	57674
rs543825539	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318231	AGCAACATTCTATTG[A/G]TAAAAAGACATTACT	57674
rs543841812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381789	CAGCGCAAGCAGGCT[C/T]GCTGTCTTGTGGGCC	57674
rs543845117	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390889	CCAACTGGTGAAACT[C/T]TGTTTCTACTAAAAA	57674
rs543846958	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392012	ACCTCAAGTGATCTG[A/C]CCGTCTCGGCCTCCC	57674
rs543854110	snp	A/C	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351483	GCTAAGAGAAGATTT[A/C]TCATCCCCTTGTGAG	57674
rs543892628	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80267429	GCCTGGCGACAGAGC[G/T]AGACTCCATCCCAAA	57674
rs543896035	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286502	CTGGGTGGGTGGGAA[C/T]GCAGCCTCCTCCTTG	57674
rs543909889	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357473	AACAGGAACAAATAC[G/T]TAGTTCCAGATAAAC	57674
rs543919302	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80291560	TGCACTCCATGCTAC[A/G]TTTGAGAATAACTAA	57674
rs543920842	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356677	CGGAACCAGGCTCGG[C/T]GGCTCCCGCCTCTCC	57674
rs543939024	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318660	CTCACTGCAAACTCC[A/G]CCTCCCGGGTTCACG	57674
rs543969531	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301098	TGTGGGTCATCTGTT[A/T]ACTCTGTTGATAGTT	57674
rs543984816	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328207	GAAAAAGTGGGTATG[C/T]GCAAAACCATCCTAG	57674
rs543986049	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335675	AAGATATCGTTTAGT[A/G]CTATTAACAGACAGT	57674
rs543988435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280966	CTGCATATGCGGACC[A/G]GAGCGTGTTGGTCAG	57674
rs544020616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334787	GACCGCCACCACGCC[C/T]GGCTAATTTTTTGTG	57674
rs544041461	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80331906	CTGTGTGCTCTTGAG[G/T]TCGCTCAGAGAAGTG	57674
rs544049033	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396202	GGGAGTTTGAGGCTG[C/T]AGTGAGCTATGATTG	57674
rs544063995	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259417	GTTTGCAGTGAGCCA[A/G]GATCACGCCACTGCA	57674
rs544081244	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80329019	AATTTCTAATTCCAT[C/T]GCAATCTCTGCCGAG	57674
rs544105894	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80296080	GCTGGAGTACAGTGG[C/T]GCAATCTTGGCTCAC	57674
rs544115136	in-del	-/AAAAAA	0.011928	0.0763002	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354819	TCATACTAAAAACTT[-/AAAAAA]AGTAAAACATCTGTT	57674
rs544126121	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372798	TTAGAAATTCAGGAA[G/T]TATGGGAAACTAGTT	57674
rs544169176	snp	G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396819	GGGGATAGCCCTTTT[G/T]AGGAGGTGGGGGTGT	57674
rs544174730	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305538	GGCTACCCCATAGGA[C/G]CATGCCCAGAATGGC	57674
rs544192383	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80311481	TGTTTCGTTTTCTGT[C/T]GGCCCCCGCCCCCTG	57674
rs544225649	in-del	-/GGATTTGACTTG	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80338080	CCAAGAAAACGGAAA[-/GGATTTGACTTG]GGATTTGACTGATAA	57674
rs544242473	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386582	CCATACTTGGGTAGG[A/G]TTTTCCACTGCTCCA	57674
rs544263205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263570	TGTGATTTCACTTTC[A/G]CAGAAAATGAAACTG	57674
rs544282105	in-del	-/CC			intron-variant	RNF213	GRCh38.p7	17:80281334	CACCACTCACACACG[-/CC]CCCCCACACACACAC	57674
rs544305759	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80339624	TGTGGGAGTGAGGCC[A/G]CCAGGTACCGCATGA	57674
rs544306543	snp	G/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370950	CCACTATGAGCTTGT[G/T]AGCTTTTGAATACTT	57674
rs544313304	snp	A/G	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80306809	GTGAGCCGAGATCAC[A/G]CCGCTGCACTCCAGC	57674
rs544328728	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392555	CAGGATGCTAGTCCC[A/G]GTTCAGGAGCTCAGG	57674
rs544351418	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80311727	TCCTCTTGCCCAGCT[A/G]CCTCGAGGCGTGGGC	57674
rs544368711	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283012	CTGATTCAATATTTT[A/G]ATGTAAAACAGCATC	57674
rs544380600	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375651	GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG	57674
rs544380790	snp	A/G	0.000715417	0.0188996	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385503	TTTCAGGGGGTTGCT[A/G]TCATACGGTTCTTAC	57674
rs544383396	snp	C/T	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389984	CCCTGCAGGCTTTAA[C/T]GCTTCATTTGCTCTT	57674
rs544433595	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307924	TTGGGTTTATCTCCC[C/T]CTGATCTTTTTTCCT	57674
rs544434464	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285169	TGTCCTACAACTCTC[C/T]GTGTGCTTTGTCCCA	57674
rs544454430	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290003	AGGTGGAGGGGGGTG[A/G]GCACCTGTGCCAGTT	57674
rs544482483	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356254	TGATCCACTCGCCTC[A/T]GCCTCCCGAAGTGCT	57674
rs544489840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305023	GATTCATCCATCTCA[A/G]TGAATTCTTTTTGTG	57674
rs544517660	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360681	CCAGCTGTGTCTCCC[A/G]AGTCACAGCCCAGAC	57674
rs544533590	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321926	AGACGGGGTTTTGCC[A/G]TGTGGGTCATGATGG	57674
rs544540215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285496	GGACGATGGGTGCCT[A/G]CAGTGAAGGGTTGTG	57674
rs544543610	snp	C/T	1.65119e-05	0.00287327	synonymous-codon	RNF213	GRCh38.p7	17:80345496	GATCCCCCAGGCCAC[C/T]GACCCCGACAAAACG	57674
rs544548909	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385996	TAACTTGTGTCTCTT[C/T]TGATGGTGGTGTCTG	57674
rs544573928	in-del	-/AGAA	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359640	GAAAGAAAGAGTGAG[-/AGAA]AGAAAGAAATGGAAT	57674
rs544595635	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270332	CATGCTTGCACGGAG[A/G]CCTTGCCCTCTGAGC	57674
rs544599369	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381101	CGTTTTGGAGATAAT[C/T]AGTCTACAAAGTAAT	57674
rs544601828	snp	C/T	9.94596e-05	0.00705123	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367734	TAATGACTCCTGTCC[C/T]TGCCTTTCTTCAGTG	57674
rs544621411	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380752	CTCAGCCGTAAGCCT[C/T]ACTCCAAGTGCTGAG	57674
rs544637752	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364017	AGGGAGCGCACTGTG[C/T]ACTGGGGCCGTAGAA	57674
rs544647189	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80286123	CAAGTGTGCCATTTC[-/A]AGCAGTGGTGCTTGC	57674
rs544659162	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269843	TGCTCTCTGGATAAC[C/G]CTGTTCTATACTGTG	57674
rs544688434	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394794	GTGCCACCAGTGTCT[C/G]ATGAAGGGCAGAGTG	57674
rs544691113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294352	TAGTGGGGGGATGCG[A/G]TTTCTGTATGACACA	57674
rs544692355	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80289496	TCGGGAGGCTGTCGC[A/G]GGAGAATTGCTTGAG	57674
rs544708134	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364904	CTGGCCATCTGTGGA[A/G]GCTGTTACCATTTTC	57674
rs544714392	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370807	ATACAGGTGTCCAGG[G/T]CTGGGCAGGCCTCTC	57674
rs544746780	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370067	ATGAGTTTAGTATTC[C/T]CACAAGCACACGCAT	57674
rs544750030	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389650	GGGCTGTGAGGTGCC[A/G]CAGGAGGGAACTGGT	57674
rs544768105	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284212	AATACAAAAAAAAAA[A/T]AATTAGCCGGGCATG	57674
rs544776869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374196	TGTGGTGCGGTGCGC[C/T]GCAAACGGAGGAAGC	57674
rs544796249	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80316917	CAAAGTATAACATGA[A/G]AGATAAGTCCTTTCA	57674
rs544819718	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80284757	TCCCGTTACTCCCTC[A/G]TGCCACACAGTGGCT	57674
rs544826632	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303959	CTGATAACAGAAGAG[G/T]CCACTAGATGATCAA	57674
rs544827891	in-del	-/AGAG	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381868	AATGAGAGAACACAC[-/AGAG]AGAAAACCGTGTCTA	57674
rs544867134	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355131	TTTAAGACAGACTCT[C/T]AGACCTCCTGCCTGA	57674
rs544868042	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80269444	ATCTATTCTATCTAT[C/T]CATCCATCTATTCAT	57674
rs544869292	snp	A/T	0.000114188	0.00755519	synonymous-codon	RNF213	GRCh38.p7	17:80337868	GCACTTGATCCTTCC[A/T]GAGAGCCCTGGCAGC	57674
rs544880220	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80292672	CTTCATGCCTCTCTC[A/G]GGGGTCCCCCACCTG	57674
rs544900287	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368906	TCCCCTTCCCCCCTT[C/T]TCAGGCCTCCTAAAA	57674
rs544907508	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80351251	TACTTGGGAAGCAGA[C/G]GCAGGAGGATCGTTT	57674
rs544923206	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350072	CATCTCCATCATCTT[C/G]TGCAACGCGGTGTCT	57674
rs544936926	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368287	AAGAGACGCCACTTA[C/T]GTACTTTCATAAATA	57674
rs544948064	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80262232	GTGGCAGGGGTAGGG[G/T]AGTTTTAAACTCTCC	57674
rs544976808	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293537	CGGTTAAAAGGGCAC[A/G]TGGTGGCTGGGCGTG	57674
rs544999800	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262716	TCTGTTTTGGGGTGG[C/T]ATAGATTAGTCTCCC	57674
rs545013601	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298296	GGCCAGCTCAGCTCA[C/T]TGCGGGATCTTTATT	57674
rs545014063	snp	A/G	1.65938e-05	0.00288039	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360119	AACCTTTCCGAGAAC[A/G]CTTCCAACAACGTCC	57674
rs545038204	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382743	TTTTTTTCAAAATGG[G/T]TCTAAGATTACAATT	57674
rs545039758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80332720	TGTGGCTTTGAAAAG[A/G]GGGGCGGATGACTTA	57674
rs545053271	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262255	AACTCTCCTTCTACT[A/C/G]TGAAGGAGAGATAAT	57674
rs545060242	snp	A/G	0.00202531	0.0317578	missense	RNF213	GRCh38.p7	17:80339897	GAGGTGTTGCCAGCC[A/G]CCCTGGCTGTCTACA	57674
rs545073890	snp	G/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356981	CTGGAGTGCAATGGC[G/T]CGATTTTGGCTCACT	57674
rs545101521	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348494	GCAGTGCACCATGCT[G/T]GTAACAGCACCATAC	57674
rs545101774	snp	A/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287519	ATAAATAAATAAATA[A/C]AAATCCATCTCAGTG	57674
rs545104369	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282891	TTAGTAGAGATGGGG[C/T]TTCCCCATGTTGGCC	57674
rs545113219	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364300	AGTATGTCACATAGG[G/T]CTTGCTTGTAATCCC	57674
rs545115920	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80278113	TACTTCCTGTGGTGA[A/G]GGAAGAGGAGACTGC	57674
rs545133601	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395433	GAAGTAGTGTGTTCA[C/G]ACTGTGCACACAGAA	57674
rs545152182	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80295135	TTTCCAGCCTTTTCT[C/T]CTACCACTGTCTCTT	57674
rs545160103	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380074	CAAAACCTGGGCATC[C/T]GTCTGTCTCAGCAGA	57674
rs545163414	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326589	CTGCCCCTACAAAAT[C/T]CCATGCTCCACCCCT	57674
rs545213758	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80337276	TGGTAGAGAGGCAGG[C/T]GGGCGGCTGCTCATT	57674
rs545214006	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80330380	CTGCGGGGTGCTGCC[A/G]TGGGGTGCTGTGGCT	57674
rs545216830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384474	TCTACAACACATTGT[C/T]TAAACATTTCTCTCC	57674
rs545244116	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338666	AAAAAAAAGATAATT[A/T]AAAAAAATTAAAACA	57674
rs545264314	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298590	GTGCACCCGGAGTCC[C/T]GGTGGGCTCTGCAGT	57674
rs545284299	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261110	TGACCCTGTTCCCCG[A/G]CTGCGGGAGGGGTCG	57674
rs545362615	snp	A/G	0.000280064	0.0118302	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358399	CAGGCCAGATACTCC[A/G]CCCTGGGCAAGAGAT	57674
rs545367040	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384000	CCTGAAGGCCCTGGG[C/T]TTTTACGTAGTATAA	57674
rs545389711	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379321	AGGGATGGAAAAAGT[A/G]CTGAATACAAGAAAG	57674
rs545402429	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389044	ACACCGTGCGCCCAA[C/G]TGTCAGCTGTTAGAG	57674
rs545407550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312815	CGTATCTCCCACGTT[C/T]AGGGTGAACCCAGAA	57674
rs545411709	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357525	GATCTGGGACAAATT[C/T]ATTTTGGTCTCTTCA	57674
rs545418263	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324879	TTCGAAGAAATGTAA[A/C]GTGTTTTACTATTTT	57674
rs545434915	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278485	TGGCAGGGTGCCGTG[A/T]GCCTGGCAGGGTGCC	57674
rs545471017	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368967	TTCTTTGACATACTT[C/T]GGGATATTGAAGGGT	57674
rs545493554	in-del	-/TTG	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80262442	GTGTGCAGGGTTGTC[-/TTG]TTGTGCAGATAATCA	57674
rs545508410	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80282599	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	57674
rs545512150	snp	A/G	6.61638e-05	0.00575131	synonymous-codon	RNF213	GRCh38.p7	17:80348016	CTCGGACGCCTGCGC[A/G]TCTGTGGTGCTGCAG	57674
rs545544133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308629	GGAGCCAATTCCACA[C/T]GGGCTGCACGCTCTT	57674
rs545544798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362596	ATAGCCAGGCCACGC[A/G]GCTGACAGTGTAGCG	57674
rs545560954	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80324359	ACTGAAATGATCATG[C/T]GATATTTTCCTAATG	57674
rs545576227	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387667	ATCCTGTGCCGGATG[C/G]ACCTGCCTGGCCTCT	57674
rs545583460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261527	GGAAGGAGCTGTGCA[A/G]ACATGGTGGTGGCCC	57674
rs545604183	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358210	TAATGCTCAAGAAGG[A/T]ACAAAATGTCAAAAG	57674
rs545617029	snp	G/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80318338	CGGCTCGAAGGTGGG[G/T]TTTTGCCAGGGACCC	57674
rs545618914	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302348	GATTTGTACACATTA[A/T]ACACTGTATGCATAT	57674
rs545685485	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287615	GAGCGCTTCAAGGCC[A/G]CTTGCCCCGACCCTG	57674
rs545697690	in-del	-/GA	0.000383784	0.0138472	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393308	AGCCACCATGCTGAG[-/GA]GACTGTTTTAAATGC	57674
rs545702541	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80323014	GTTTTATAGTTTTAG[C/G]TCTTACATGTAGGCC	57674
rs545721414	in-del	-/G	0.0748431	0.178382	intron-variant	RNF213	GRCh38.p7	17:80276087	ATTTATTTATTTATT[-/G]TTTTGTTTTATTTAT	57674
rs545731014	snp	C/T	1.65586e-05	0.00287733	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369808	CTCTCCATTCAATGA[C/T]GTTGTGGATAAGACT	57674
rs545734816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301922	GAAGAAAGTGTTGTC[C/T]ATATACACAGTAGAA	57674
rs545737611	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388125	CCCGCCACCATGCCC[A/C/G]GCTAATTTTTTTGTA	57674
rs545741904	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312419	GCACAGTGGGAAGGG[C/G]ACCCAGGTTTACCTC	57674
rs545749220	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80280797	TTTTAAACTATAAAT[G/T]GGTGAGGATACTTAA	57674
rs545760501	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393644	AAGACCAAGGCGTGC[A/T]ACCTGAGCTGACAGC	57674
rs545792551	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80281800	TGCCCAGTCCCAGAT[A/G]TGAAACGGCGTGGCA	57674
rs545798878	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397170	GGCTCCTTCACCCTG[A/G]CCACTCTGGAACCCA	57674
rs545843989	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80262399	TTTTTATGGCATTGG[A/G]ACAGGGGCTTGGGGC	57674
rs545852277	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277385	GGTGGATCACTTGAG[A/G]TCAGGAGTTCAAGAC	57674
rs545854490	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80271851	TGGGTGTGGTGGCGC[A/G]TGCCTGTAATCCCAG	57674
rs545878433	in-del	-/T	0.280785	0.248097	intron-variant	RNF213	GRCh38.p7	17:80318578	AGTTTTATATGTAAC[-/T]TTTTTTTTTTTTTGA	57674
rs545885362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291075	CCTAGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	57674
rs545885950	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80299103	TCGTGGGTGTTTTAT[G/T]TACTTAAAAGAACAA	57674
rs545892944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297265	GACCAGCCTGACCAA[C/T]ATGGTGAAACACTGT	57674
rs545897810	snp	C/T	8.23621e-05	0.00641672	synonymous-codon	RNF213	GRCh38.p7	17:80290612	CGTGTTCTTCCACGC[C/T]ATCATCTCTCTTCAT	57674
rs545936571	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392078	CGGCCTGTCCTCTCT[C/T]TTCTTGTGCTTTCAC	57674
rs545946438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372830	TTCGAATAGACTACT[A/G]CTGGGCTTTTCTACA	57674
rs545957442	snp	A/G	0.0012347	0.0248158	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376316	CAATGTGAAGCTGTG[A/G]GCAAATTCATTGGCG	57674
rs545963983	snp	A/G	1.64773e-05	0.00287026	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361805	GCCCAGCTCCATGGA[A/G]AGCCGCAGCAGGAAC	57674
rs546026951	snp	C/T			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321578	TTGTTTAAAGAACTG[C/T]CCGGCCGAGTCCCAC	57674
rs546051766	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381948	CAGAGGCTGGAAGGA[G/T]CTGCTCTGTTCCCTC	57674
rs546063885	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80295268	GGAAGGAACGGGGCA[A/C]CCTCTGTCACTGCAC	57674
rs546068285	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349989	GATGGTACCCGCGCC[A/G]GTTAATGAGCGCCAC	57674
rs546068805	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365218	CCTCACCGCCAGGGG[G/T]TCTGGAAGAGGCAGC	57674
rs546070479	snp	A/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80277048	GCAACAGAGCGAGAC[A/T]CACTCTCAAAACAAA	57674
rs546074794	snp	C/T	0.000133409	0.00816619	synonymous-codon	RNF213	GRCh38.p7	17:80346609	CATGATGGTCGTCTG[C/T]ATCGAGCTGAAGATT	57674
rs546111416	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80264632	CTCCTTCCTCCATGA[C/T]CCACATGCAGAGGGC	57674
rs546120921	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376825	CTCCTGCTGAGCAGC[A/G]GCACCCAGGTGACAA	57674
rs546134996	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365835	TCAGCCAGGTCCAGC[A/G]TGGGTCATAAGGGCC	57674
rs546144271	snp	A/T	0.0777841	0.181223	intron-variant	RNF213	GRCh38.p7	17:80271159	GCTCAGAATCCCTGG[A/T]TGTAGGTGAAACAGC	57674
rs546213521	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80306678	AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT	57674
rs546214039	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80279818	TTACAGGACTCACTA[A/G]TAATATCAAAAATGA	57674
rs546216561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274059	TGAGGGTGCAAGCTC[A/G]GAGGTGCCTTGCTGC	57674
rs546228114	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360931	TTTCTCAGGACAATA[C/T]CCCAACTGACCCTGC	57674
rs546228274	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363529	TGGGACACAAGTATA[C/T]ATGCAGCTAACAGCC	57674
rs546234821	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80305703	TGCAATCTCTGCCGC[C/T]GGGGCTCAAGTGATT	57674
rs546234906	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330211	TCTGGGTTATTCACC[A/G]TTTTGTTTTGGAGGT	57674
rs546238715	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80322562	GCCTGGGCGACAGAG[A/C]GAGACTCTGTCTCAA	57674
rs546271475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286399	GCAGGAAGTGTGGCC[A/G]TGTGTGATAGAGAAG	57674
rs546277773	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397267	TTCTACAGCCATGGG[C/T]AAGTGGCTCGACCTC	57674
rs546291544	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387795	GCCCATTTCCCTGAA[C/T]TGCATCCCGTGACCT	57674
rs546302954	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356937	GGTTTTTTTTTTTTC[A/G]AGACAGAGTCTCACT	57674
rs546304940	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395098	TTCTGTGAAGGCTTT[C/T]TTTTTCCTTTGGCCT	57674
rs546335184	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375562	AAAAAAAGAATTAGC[C/T]GGACATGGTTGCGTG	57674
rs546346306	snp	A/C	6.5912e-05	0.00574035	missense	RNF213	GRCh38.p7	17:80346086	TGTGGGACTTTGGAC[A/C]ACTGAGTGACGTTGC	57674
rs546374586	snp	A/G	0.00659603	0.0570483	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389785	GACATGAGTGGGGGT[A/G]TGAGACCTCAGCCCC	57674
rs546413087	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341114	GGCCTAATTTTTGTA[G/T]TTTTAGCAGAGACAG	57674
rs546424141	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381225	CACTCTGTGTCTCTG[C/G]TCCACATCTGGGAGT	57674
rs546472244	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355259	CTGTGCCAGTGATAG[C/G]TTCGCTTTGGGCCTA	57674
rs546474496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334943	TTTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG	57674
rs546474616	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341517	TCACTCAACACATAA[A/T]GACATTTCAGTCAAC	57674
rs546478345	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279410	AGCCCTGCTCAGTTT[A/G]GTCTCTGGTTTTTGG	57674
rs546534418	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385241	GATCACTGCATAGGG[C/G]AACAGGGTGGGGCGG	57674
rs546538292	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320685	GTGAGCCACCGCGCC[C/T]GGCCGAGCATAATGT	57674
rs546556913	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80349787	CACCACTTTCTCCAG[A/G]CTGCTAACAAGTCAC	57674
rs546594363	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385685	CTGAAAGCTCTTCTC[A/G]TCAGCCTGACTCGGC	57674
rs546638783	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378072	TGACCTCGAGTCCCT[A/G]GATGCCAGGAGCACC	57674
rs546643996	snp	G/T	0.000509332	0.0159501	stop-gained	RNF213	GRCh38.p7	17:80317251	AAGGAGTCGTTGCTG[G/T]GAGACATGGAATGGA	57674
rs546652833	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368542	GGTTCAGGCAATTCT[C/T]CTGCCTCAGCCTCCC	57674
rs546687179	snp	C/T	0.000130745	0.00808426	missense	RNF213	GRCh38.p7	17:80339964	AGGTGCTGCTCTGCA[C/T]CCCGGCAACCACCTT	57674
rs546696997	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80338896	GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG	57674
rs546731186	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325909	AAGTAAAAGCTACTC[C/T]CTTGAAAAGATCATT	57674
rs546739266	in-del	-/A	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396996	ACCTAAACTTACTAT[-/A]AAGGGTCCTACCTTC	57674
rs546741310	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262969	GTGCCCTGAGGCTTC[C/T]TACTGGGGAGGGAGA	57674
rs546742735	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289201	AGGCGCCTCTGGAGG[C/T]TGTGATTAGTGGCCC	57674
rs546772780	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320376	GTTGTTTTTGAGACA[A/G]AGTTTCACTCTTTTT	57674
rs546848646	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367689	CTCCCTCTGTCGCCC[A/G]GCCTGGCCGCCCTCA	57674
rs546855705	in-del	-/GA	0.00119737	0.0244387	intron-variant, frameshift-variant	RNF213	GRCh38.p7	17:80288907	GCTCACATTCCAGCG[-/GA]GAGAGAGAGTCAGGA	57674
rs546863629	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308762	TTTCACATCTTGGAA[C/T]GCACTGAGGAGTGTT	57674
rs546878597	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80316979	CAGTAGTGGCCCCTG[C/G]TTGGGTCTCTGATTC	57674
rs546920732	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348688	CTTAGAGGCAGCGGG[G/T]AGCGGTGCAGACCAG	57674
rs546946917	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80281998	AGCAGCTGGGACTAT[A/G]GGCGCCTGCCACCAC	57674
rs546986538	snp	A/G	0.000131798	0.00811675	intron-variant, missense	RNF213	GRCh38.p7	17:80319320	CCTGCCAGGTGAACA[A/G]TCTCTCCTCCTGGGA	57674
rs546995134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393135	AGGCATACACCACCA[C/T]GTGCCCAGCTAATTT	57674
rs547009752	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80269060	CAAGGGCAAGAGGAA[C/T]GTGAGGAAGCATCCA	57674
rs547050750	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319597	CACGGGCTTGCAGGC[C/T]GTTCCTCAGATGGCC	57674
rs547066283	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364112	CAGGTGCACAGAGCA[C/G]GACAGGCCCTCAGGG	57674
rs547095530	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293254	TTTTTGGAGAGACTG[A/G]TCTTGCTGTGTTGCC	57674
rs547103075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369164	AGCACTCTGGGAGGC[C/T]GAGGTGTGTGGATCA	57674
rs547112793	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324603	TTTCTCGGAGGAGAA[C/T]TAAAAAGAGAATTAA	57674
rs547125953	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325454	GGGTCGCAAGGGAAG[C/T]GCCCTTGAAACAACC	57674
rs547144838	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297029	GCACATTTTGACAAA[C/G]AGGAGGAGTGGAGGC	57674
rs547154763	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292793	TCCTGGGCTTCCCCT[C/T]GCTCCCCCTCCCTGC	57674
rs547156918	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80298793	AACATGGTGAAAACC[C/T]GTCTGTACGAAAAAT	57674
rs547158013	snp	A/G	0.000839983	0.0204765	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353655	GAAACCTCTGAACTC[A/G]GAGGCAGTGATGTAA	57674
rs547183503	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394472	GGGAAAAGAGTCCCC[A/G]AGCCCGGATCTTGTG	57674
rs547197680	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379311	TGATAGATGGAGGGA[C/T]GGAAAAAGTGCTGAA	57674
rs547202101	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378326	GTAGGCTGTGCGCCA[G/T]GGGGGAAGAACTGTT	57674
rs547206206	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80302100	TCTTCTAGAAGGAGA[A/G]AGTAGAATAGTAGTT	57674
rs547217901	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372816	TGGGAAACTAGTTCT[C/T]CGAATAGACTACTAC	57674
rs547239582	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344242	TTCAATATTTCTGTT[C/G]AATTCAGGCTTCATG	57674
rs547242853	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278214	AGCTTCCTGCTGGGC[A/G]TCTTGCTGTGAGGTC	57674
rs547259103	snp	A/G	3.35576e-05	0.00409606	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354019	CGTCTCCACCAACAG[A/G]TGTCGATCCTGGACA	57674
rs547263527	in-del	-/TAA	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80265365	GGGCTCCACTTCTAT[-/TAA]TAATAGTGCGGAGAG	57674
rs547268084	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359991	GAGCTGGCATCAGTG[A/G]CAGATCTTATCTTGT	57674
rs547317243	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309375	GGCCAGGGTCTGCCC[G/T]TCTGCCACCTTGGGC	57674
rs547324503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267224	CTCTGTCTCAAAAAA[A/G]AAAAAGAAAAAAAAG	57674
rs547328221	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80297401	GTTGCAGTGAGCCGA[A/G]ATTGTGCCACTGCAC	57674
rs547328864	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363377	ACTCCACTCTGGGAA[C/T]GGAGAGCTTCTGGGG	57674
rs547331626	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278708	TTGCGAGTCTACTGG[A/C]GCTGTGCGTGGGGTG	57674
rs547335318	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80292105	TTTTGTTTGTTTGTT[C/T]TCTGAGACAGAGTCT	57674
rs547345073	snp	A/C	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80330598	TCACACCCCATCCTC[A/C]TTCCCCCTGAGATTG	57674
rs547372782	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382921	TAGGGTTTATTATAC[A/G]CAGACTGCTGTGTTC	57674
rs547376537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358154	AATGTCAAGTTATTG[C/T]TGTCGCTGTAGTGTG	57674
rs547393179	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384068	ATAGGATGTAGCAGA[A/C]GACTCAGGGCTAGAG	57674
rs547402004	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331537	GGGATTACAGGTGCG[C/T]TCCACCACGCCTGGC	57674
rs547413980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276775	AAATTATCCTAGGCC[A/G]GGCGCGGTGGCTCAC	57674
rs547417713	in-del	-/T	0.000395759	0.0140614	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369711	CTAGCCCCTCATTTC[-/T]TCATCTCGCTTCTGC	57674
rs547459067	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80312632	GAGCCTGGCTGTCTC[C/T]TGTGTCTAAGGAACA	57674
rs547491143	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377101	GCATTCTACCGGTGG[C/T]GTCTGCAGAAGACGA	57674
rs547494182	snp	A/C			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259295	CAACATGGAGAAACC[A/C]CGTCTCTACTAAAAA	57674
rs547496503	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387865	GTTCTTTGACTGGAC[A/G]CACTTGTTCCTTCCA	57674
rs547516437	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282613	CCGTGTTAGCCAGGA[G/T]GGTCTGGATCTCCTG	57674
rs547534768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358534	CAGAACACAGCAGGA[C/T]CCTAATATGCTCTCC	57674
rs547537528	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80301649	CAAAAAATAAATGCC[A/G]GTGAGGATGTGGGAA	57674
rs547543714	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361488	TCACGCTACCCACCG[C/T]ACTCCAGCCTGGGCA	57674
rs547556838	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80267842	TTTTTTTTTTTGAGA[C/G]AGGGTCTTGGTCTGT	57674
rs547565287	in-del	-/TCTC	0.00217707	0.032921	intron-variant	RNF213	GRCh38.p7	17:80342537	CTGGGACTTAATTTT[-/TCTC]TCTCTCTCTCTCTCT	57674
rs547586254	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259463	TAGAGTGAGACTGTC[C/T]CCAAAAAACAAACAA	57674
rs547589754	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260299	GCTGGGCGCCGGGGC[G/T]GGGGGCGCGCCTGTC	57674
rs547593431	snp	G/T	6.59196e-05	0.00574068	missense	RNF213	GRCh38.p7	17:80347716	CCTCGGCGGCCAGAA[G/T]TACGTGGACCTCGGT	57674
rs547600333	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326226	ACCTCCCGGGCTCAC[A/G]TGATCCTCCTGCCTC	57674
rs547656580	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80343059	GTGATCCCCCCGCCT[C/T]GGCCTCCCAAAGTGC	57674
rs547666139	snp	C/T	6.61857e-05	0.00575226	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367740	CTCCTGTCCCTGCCT[C/T]TCTTCAGTGTCTTCG	57674
rs547674858	snp	C/T	0.0221141	0.102801	intron-variant	RNF213	GRCh38.p7	17:80281333	CACACCACTCACACA[C/T]GCCCCCACACACACA	57674
rs547677036	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357626	ATTTATTTAGAGAAC[C/T]TCGATGACTTGTTCT	57674
rs547690593	in-del	-/AGG	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80349364	AGTGACCTTTGGGAC[-/AGG]AGAATTGCTGACATC	57674
rs547702945	in-del	-/A	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356941	TTTTTTTTTCGAGAC[-/A]AGAGTCTCACTCTCG	57674
rs547706720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329128	AGTCTCCCTCCACCT[C/T]CTAGGAGCCTTTGCC	57674
rs547707350	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362757	TCAGCTTTGCTTCGA[A/T]AAATAAGAAATAGTT	57674
rs547713682	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361949	GATGGGGACTGGATG[C/G]AGACACGGAGACGTT	57674
rs547723495	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337025	GGACGGCTGCTCTGC[A/G]TGTGGGTGGAGGAAG	57674
rs547731237	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355833	TACAGGAGAAGAAGC[A/G]GGGTGAACGGGAATG	57674
rs547752727	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390478	CTTGGCTCACTGCAA[C/T]CTCTGCCTCCCAGGT	57674
rs547760759	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265496	ACTCTGTACATGATG[C/T]TTTTGAACATTTATC	57674
rs547778696	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80286543	GGGCCGACCGTCAGC[C/T]GAGGGGCTCCTGAAG	57674
rs547828667	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341293	TTTGGGGTTGATGTT[C/G]GTCGTGTGAGCAAGG	57674
rs547832363	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318735	CCCGCCACCGCGCCC[A/G]GCTATATTTTTGTAT	57674
rs547846490	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266191	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	57674
rs547846539	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259094	CTGGAGTGCAGTGGT[A/G]CAGTCAAGATTGGTG	57674
rs547889652	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341729	GGCAACGGGGCAAGG[C/G]CTTGGTCTTTTAAAA	57674
rs547895044	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80342431	AGCGTATTCTTGAAT[C/T]TGATGTTATGTTGCA	57674
rs547902206	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286989	TTTTTTAGTCTCATC[C/T]TTCTCATTTCAAATT	57674
rs547920453	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80324258	CAGTTTGTGGAAGTT[-/C]CCTTTTTGTTCCTCA	57674
rs547924816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270935	GTTTCCCAGCACCAC[C/T]TCATGGTCTTTCCAG	57674
rs547948226	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335746	TTTGGGAGGCCAAGT[C/T]GTGTGGATCACCTGA	57674
rs547953245	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80335797	CCTGACCAACATGGT[A/G]AAACCTGGTCTCTAC	57674
rs547967539	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80317923	CCGGACACTTGAAGG[A/T]TGGTGAAGGTGGAGA	57674
rs547974182	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392299	AGCCTGTGCTTTTCA[C/T]GTAGATAAAAAAGAT	57674
rs547976120	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365962	GCGATAAAATGGCCT[C/G]AGAAACTTACTGGGT	57674
rs548010168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322596	AAAAAATTTTTTTTC[A/G]TAGAGACAGGGTCTT	57674
rs548012266	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398163	TTGACTTGGATTGCT[C/T]GATACTTTGGTTTTG	57674
rs548051468	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352095	GTTGACCTCATGATC[C/T]GCTCGCCCCAGCCTC	57674
rs548057300	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391462	TTTTAGTACAGAGAC[A/G]GGGTTTCTCCACGTG	57674
rs548065555	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287231	CTGGGAATGGTGGTT[C/T]GCGCCTGTAATCCCA	57674
rs548066921	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80323541	TTAGATTTTTTTTTT[C/T]CCCCTGTTAGACAGA	57674
rs548071146	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80318435	CCAGGCCTGCCCATA[A/G]GCAGGAAGTCTAAGT	57674
rs548089896	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357369	TTCATCCATCCCTCC[A/G]CCTGCCTGTCCATCC	57674
rs548129127	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80333224	CGGCTAATTTTTTTG[G/T]TATTTTTTTTTTTTT	57674
rs548129890	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80264395	GGAGCGGGGCAGTGT[A/C]AGGCGGGCCTTGCCT	57674
rs548132589	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373254	CTACCCTCACACCCT[-/A]CCCCCCCCACACCCC	57674
rs548142605	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395798	TTCCAAAAAGGAAAG[G/T]TTCTTCCAGGCGAGA	57674
rs548145405	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275557	CGCACTCGAAAAAGA[A/C]CTGAGAAGACCTCAG	57674
rs548160555	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318935	GGAAAAATGACCTAT[A/G]TCTCATAACTTACCT	57674
rs548217729	snp	A/G	4.94181e-05	0.00497057	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376394	CTCGTGGACAATTCT[A/G]TGCCATTGTTGAGGG	57674
rs548223366	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320083	AGTTCAGCAGGTTTT[A/G]GGGTAGTCACAGATA	57674
rs548223475	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296399	GAGGTTGTGGCGTGA[C/T]GCCAGCCTGAACTCA	57674
rs548238429	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80328569	TAGCAGATCTTTATT[C/T]TGGAGAGAAGGCTTT	57674
rs548246798	snp	C/T	0.0535932	0.154675	intron-variant	RNF213	GRCh38.p7	17:80290456	ATGTGTGTGTGCGAG[C/T]GCATGTGTGTGTGCA	57674
rs548260437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294477	TCCCATGACCCTGGG[C/T]TTTCCACTCATTACT	57674
rs548273024	snp	C/T	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80335209	GTGAGCAAGTACAGG[C/T]GTGAGCCACCGCGCC	57674
rs548285142	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80327575	TGATTTTGGCCATTG[A/C]GGGAAGTCATCTTCT	57674
rs548287951	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296157	CCTTAGTAGCAGGGA[C/G]TACAGGTGCACACTA	57674
rs548288890	snp	A/T	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80293067	AACATATATATATAT[A/T]TTTTTTCTGAGACAG	57674
rs548294804	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370294	CTATTTCCTTGGAAA[A/G]GATGTTGACATCCAA	57674
rs548294893	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390442	CTGGAGTGCAGTGGA[C/G]TAATCTCAACTCACT	57674
rs548320830	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350802	AGAGCCTGTCCTCCC[C/G]ACAAAAAAGGTGAAA	57674
rs548329633	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298867	GCTTGTAATCCCAGC[A/T]ACTCTGGAGGCTGAG	57674
rs548331570	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305205	TTTTTTTTGAGACAG[C/T]TTTGGTCTCATTGCC	57674
rs548333936	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396870	CAAAGCAGGGGGAAG[C/T]AGGAGAGACTGGAGG	57674
rs548348526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301156	TTAATTAGTTCTTAT[C/T]TGTCAATTTTTGCTT	57674
rs548388664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380778	CTGAGAAAGTGCAGC[A/G]TGCCAAAGCGGCCAG	57674
rs548400771	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290055	GGGGTCCTGGAGCCA[G/T]CGTGGGCCTTTGGGA	57674
rs548423173	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355372	TGAACGGGAATGGGA[A/G]CTTACAGGGGAAGAA	57674
rs548440215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280406	ACGGGAACTTAACCA[A/G]CTAATTAATGTATAA	57674
rs548445974	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360964	TTCTATGACAGCATG[C/T]GAATTAGGGGCTGCA	57674
rs548446666	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80301789	CGTACTGCTGGGGAT[A/G]TATCCAAAGTAAAGG	57674
rs548464681	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369259	CAAAATTAGCCAGGC[A/G]TGATGGTGCGTGCCT	57674
rs548488872	snp	C/G	0.0410537	0.137264	intron-variant	RNF213	GRCh38.p7	17:80274780	GTGTGAGTGGGGTGT[C/G]TGTGGGGGATGAGTG	57674
rs548494211	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392809	TGGCTAGGCTGGTCT[A/C/G]GAACTCCTGACTTCA	57674
rs548528161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280755	CCACCACCCTAGCCT[C/T]GTTTTGTATTTTTGG	57674
rs548543833	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80339129	TGGCGGTAGGCCTGT[G/T]TGCTGTTGCAGAGTA	57674
rs548550477	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80308265	CTGTGACTTGAGGAT[-/C]CCCCCCCACAAGCTC	57674
rs548552861	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381846	TGTCTGTGCTGTTGC[C/T]GGAAAGAATGAGAGA	57674
rs548594056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384788	TCAGCCTTTGATGGA[C/T]GCGGCTGATGCGTCA	57674
rs548606404	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80284310	CGGAGGTTGCAATGG[A/G]CTCAGATCATGCCAT	57674
rs548607878	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333109	GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC	57674
rs548659875	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80335194	TCCCAAAGTGCAGGC[G/T]TGAGCAAGTACAGGC	57674
rs548684524	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309535	CTGTTGTTTGCAGAG[A/G]ACTACGGGGACCATT	57674
rs548702600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391016	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC	57674
rs548716336	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380514	GCTGTTCTTAGCCCA[A/G]CCGCTCCTCTCCTGA	57674
rs548721904	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80316450	AATGACCAGGGAACT[C/T]TTCTAGAAAAGAGAT	57674
rs548735923	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279416	GCTCAGTTTAGTCTC[C/T]GGTTTTTGGAAGTTG	57674
rs548738435	snp	C/T	1.71602e-05	0.00292913	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288312	AGGCAGCTCTGAGCC[C/T]GGGACAGAACTGCAG	57674
rs548770284	snp	C/T	0.000464225	0.0152282	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363561	GGGCCTCTGGTGGGC[C/T]GGTGGGAGGGGCACC	57674
rs548770533	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262329	ATGCAAATTGTCCCA[A/T]ACACCTATTGGGAAC	57674
rs548788084	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80350080	TCATCTTCTGCAACG[C/T]GGTGTCTGGCCTAAC	57674
rs548797800	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261156	GCACGCCTGGGACCC[C/T]GGCGACATCCCCGGA	57674
rs548820786	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80330997	TAGTTTTTTGTATTT[C/T]TAGTGGAGATGGGAT	57674
rs548838459	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333642	GAGGTTGCAGTGAAC[C/T]GAGATCGTGCCACTG	57674
rs548846802	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293899	AGGAGGTGATGACCG[A/G]GTTGAGAACTAAACA	57674
rs548848152	snp	C/T	1.64947e-05	0.00287177	synonymous-codon	RNF213	GRCh38.p7	17:80345520	CAAAACGTATGAGCT[C/T]ACAACCGACAATATG	57674
rs548870148	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80290319	GGTGTGTGCGTGTGC[A/G]TTCACGTGTGTGTGC	57674
rs548917956	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354751	CAGTAGGTCTGGACA[G/T]TGGCCAAATGGCAGG	57674
rs548940465	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389722	TAGTACAGGGCAGAA[C/T]GAAGAGAAGAATGCC	57674
rs548957927	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349364	AGTGACCTTTGGGAC[A/G]GGAGAATTGCTGACA	57674
rs548998480	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354244	TCATTTCACTGTGTG[G/T]TGGGGGACACCCTCT	57674
rs549002397	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80289155	CCCAGGAGGAGTTGG[A/G]GGAGGAGAGGCCACC	57674
rs549004087	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310497	ACCTCACGTGATCCA[C/T]CTGCCTTGGCCTCCC	57674
rs549021336	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320324	GCTTATTTCACTGAG[C/T]ATAATGTTTTTTTGT	57674
rs549022683	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273956	CCAGACCCAATACTC[A/G]TGTGTCTCCCAGAAG	57674
rs549036349	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80268991	AGATCCCCCTGGCAA[A/G]CCACTGGCGTAAGTC	57674
rs549085571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373895	GTAATCCCAGCTAGT[C/T]GGGAGGCTGAGGCAG	57674
rs549104965	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80309976	AGCCAGGATGGTCTC[A/G]ATCTCATGACCTCAT	57674
rs549124491	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379239	AATATAAGGAAGTCA[A/G]TTTGGAAGCTCTTCT	57674
rs549195090	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80325802	TTTCAGTGAGAAGGC[A/G]CTGGATGTGGAACAG	57674
rs549196517	snp	C/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332226	AGAGCCGCTGAGTGA[C/G]CCTAAGGAGGACCAG	57674
rs549220949	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80337554	ATCCTCGCTCCAACC[A/G]TGGCCCGTGTTCTCT	57674
rs549250816	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80348571	CAAGGGCACTAGGGA[C/T]GCACAGATGAATCTG	57674
rs549250924	snp	A/C/G	3.30826e-05	0.00406699	missense	RNF213	GRCh38.p7	17:80343221	ACAATTCGACTGATC[A/C/G]ACCCTCAGGTGGATG	57674
rs549255270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298087	TTCTGAGATCCCTCC[C/T]CTGTCCTGGGAGTTT	57674
rs549258394	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320100	GGTAGTCACAGATAT[G/T]TACAGTCATCACCAC	57674
rs549287825	snp	C/T	0.000115595	0.00760157	missense	RNF213	GRCh38.p7	17:80348174	TGGGCGGGTTCGCAG[C/T]GGAGTGGCTGTCGCA	57674
rs549296814	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394878	TGTGATTGTTTTATC[A/G]CTCTGGACTGTGCAG	57674
rs549323653	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80265951	GGTGGCAAAGGAAGG[C/G]ATCCTTCAAGTTGGG	57674
rs549328844	snp	A/C	1.64898e-05	0.00287135	intron-variant	RNF213	GRCh38.p7	17:80319171	AAGCTCTGAAACCAC[A/C]CCCCTTTGATTTTTG	57674
rs549354812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303649	GGTCACTGCAACCTT[C/T]GCCTCCCAGGTTCAA	57674
rs549369980	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272549	GAGTAAACCCATGAC[C/T]GCAAACGGCACCAAG	57674
rs549401408	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80329828	AGAGTGGGACCCTGT[C/T]TCAAAAAATAAAATA	57674
rs549404022	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308711	TTCAAATTTATGTCA[C/T]ATTTTAATGTCTAGT	57674
rs549431813	snp	C/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80337995	GTGGAGAGGTTTTCA[C/G]AGGTGAGGGCGCATC	57674
rs549481794	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291467	GACTCAAGAAGTCCT[C/G]CCGCCTCAGCCTCCC	57674
rs549502835	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80304481	CCATCTCTACTAAAA[A/G]TACAAAAAATGAGCC	57674
rs549516789	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260157	CCGCGCGGGGCCGCG[A/G]AGGTCCCTTAATCTG	57674
rs549524074	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301241	CTAGAATGGTATTGC[C/T]TAGGTCTGGGCAAAG	57674
rs549532212	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307424	GCTGGAGTGCAGTGA[C/T]GCAATCTTAGCTCAC	57674
rs549542350	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388806	TGAGCCCACAGTTTC[C/T]GCGGCCTCCCTTACA	57674
rs549546160	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353221	TGGTGGCTCATCATA[A/G]AGCACCAGGGCCGAG	57674
rs549570398	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371370	TCCCATATGCTGCAG[C/T]GATGGGGAGCAGGGC	57674
rs549581278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382878	GCTATTACCTCAAAA[C/T]GAGTGTTATTTCTAT	57674
rs549588379	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383610	ACTGGTGGAGTTACT[C/G]GGTGTTACAATCTGT	57674
rs549600375	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358044	CCAGTAACCTAATGA[C/G]AGTTTATTAGATGTA	57674
rs549609798	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278166	TGGAGGCATCGGCAG[G/T]CCAGGAGGCTGCTGG	57674
rs549647379	snp	C/T	9.8987e-05	0.00703447	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393360	CCTGAGAGACACTCT[C/T]GTAAGTTACATGCAA	57674
rs549649922	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384057	TTTGGTTTTGAATAG[A/G]ATGTAGCAGAAGACT	57674
rs549686130	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377928	CCGAGGACTGCCCAG[A/G]GTGCTCTGAGCAGGG	57674
rs549693319	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80314344	TGGTGGTGGTGGTGG[A/T]GGTGGAGGTACTGGA	57674
rs549713795	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398320	GCGTAATGTTTTGTC[C/T]TGAAGAAGCATGGGT	57674
rs549717423	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283035	ACAGCATCCTAAAAG[C/T]TCTAGAAAATGTAGG	57674
rs549736771	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380566	CGGGTCCAGGCCTGC[A/G]TCTTAACACCCTGCC	57674
rs549741330	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80308149	AAATGTGCCAGTGAG[C/G]GATGGGATGGGTGTT	57674
rs549753282	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387326	TGCCCGGCTGGTCTC[C/G]AACTCTTGGGATCAA	57674
rs549771456	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362207	TAAATACGTAACTAA[C/T]CCTACAGGGTAAGAA	57674
rs549771680	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367336	AAAAAATGATCTATC[A/G]CAGCAGCTTGGGAGG	57674
rs549788687	snp	C/T	2.77689e-05	0.00372608	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386911	GGCTGACTCCTGCCA[C/T]TGCTGCTCATTTGGT	57674
rs549790931	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296980	CACTGTGCCTGGCCT[A/G]GTTTTACAAATAAAA	57674
rs549798816	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80286479	TCCAGCTGCGGCCTC[A/G]TCATGCCCTGGGTGG	57674
rs549808400	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366746	CATTTCAAAATGTAG[A/G]GAGAAAGCATTTGAT	57674
rs549855016	snp	A/G	4.94328e-05	0.00497131	missense	RNF213	GRCh38.p7	17:80291776	CAGCAGAAGAAGGGC[A/G]AGTACGTCAACCGCT	57674
rs549860333	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357043	TCCTGCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	57674
rs549885137	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80318353	GTTTTGCCAGGGACC[C/T]GCCCCTGTCTGCGTA	57674
rs549902359	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282141	GGATAACAGGCCTGA[C/G]CCACTGAGGCCGGCC	57674
rs549918152	snp	A/G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384404	AGTGTACTGGCCACA[A/G/T]CTGTTGGAATTGGAA	57674
rs549924308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372039	CTATCTGAACCACAT[A/G]GTTTAAAATTTACAG	57674
rs549932887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362738	GTTCACAGGGATGTC[C/T]TTTTCAGCTTTGCTT	57674
rs549937397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290299	TGCCTGTGTGTGTGC[A/G]TGTGGGTGTGTGCGT	57674
rs549963970	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365135	AGCAACAGTGGCCAC[G/T]CAGCCAAACACAGCC	57674
rs549981997	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80266429	AGAAGAAAAGAAAAG[A/G]AAAAAAAAAGCCTTA	57674
rs549983836	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386905	AGGTAGGGCTGACTC[C/T]TGCCACTGCTGCTCA	57674
rs549983909	snp	G/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80271989	CGTCTCAAAAAAGAA[G/T]AAAAAAGAAAAGAGG	57674
rs549998506	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80341942	CTCCTGAGTAGCTGG[C/G]ACTACAGGCACACGC	57674
rs550006488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265294	TCAGGTGATCCACCC[A/G]CCTCGGCCTCACAAA	57674
rs550014891	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359154	GGCCTGATGATGTGC[A/G]GCTCAGGCTCAGCTC	57674
rs550017452	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259706	ATTTTTTTTGTAGAG[A/T]TGGGGTCTCTCTATG	57674
rs550026110	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80281301	CACACATACCCTCCA[C/T]ACACACATACCCCAC	57674
rs550044956	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271445	GTGCTGGAAACGGGC[A/G]TGGGGATGAAGTGTC	57674
rs550050363	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311963	GAAACCCTGTCTCTA[A/C]TAAAAAATACAAAAA	57674
rs550055892	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80292248	TGTCACCACCCCCAG[C/G]TAACTTTTGTATTTT	57674
rs550058416	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80335955	TCACTCCAGCTTGGG[G/T]GACAGAGTGAGACTC	57674
rs550069548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267204	CCTGGGTGACAACAG[C/T]GAGACTCTGTCTCAA	57674
rs550074148	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80290442	GTGCGCGTGTGTGCA[C/T]GTGTGTGTGCGAGTG	57674
rs550081137	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80295440	GTGGCTCTCACAGGT[G/T]TGGTGGTGGGGCACG	57674
rs550089443	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80258924	TAGGGGCAGACTGTG[A/G]TCACAGAGACAGCAC	57674
rs550095153	snp	C/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80296308	TGTAGGCGTGAGCCA[C/G]CGTGCTGGGTCTGAA	57674
rs550126068	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361666	CCTTCACTCCGGAGC[C/T]CCCTGGAGGCAGGGG	57674
rs550129811	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311581	CCTGGTCCCTCTTAC[A/G]TGCTTTGAAAGCTCC	57674
rs550135477	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368700	GGCCTCCCAAAGTGC[A/G]GGGATTACAGGCATG	57674
rs550149461	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80350460	TAGGAAGTCCTAGAG[A/G]ATTTTTTCCTTGAAG	57674
rs550159401	snp	A/G	0.000792707	0.0198928	intron-variant	RNF213	GRCh38.p7	17:80336534	TTCTTCATAAATGGA[A/G]ATTCACCATCTTGTT	57674
rs550164696	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80318059	CTGAAGTCAGGACGT[C/T]TTTCCGAAGTTAAAC	57674
rs550180696	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80280886	GTGGAAACATTCCCA[C/T]GGAGTAACAGAGGCG	57674
rs550204991	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270118	TGTGTGCGCACACAC[A/C]CACACGTTAATGTGA	57674
rs550205986	in-del	-/TCTTATT	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80269913	CTAGTTAAGTATGTC[-/TCTTATT]TCTGAATCCAGCTAC	57674
rs550210894	snp	A/G	1.64765e-05	0.00287019	missense	RNF213	GRCh38.p7	17:80346134	AGCAGATTGTCCAGA[A/G]ACTGGTTGAGTCCAT	57674
rs550217337	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80264711	GCTCAGCACAGCAGA[C/T]AGTCAAACCACAGAC	57674
rs550220220	snp	C/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360107	CAGAACCACATGAAC[C/G]TTTCCGAGAACGCTT	57674
rs550244427	in-del	-/T/TT			intron-variant	RNF213	GRCh38.p7	17:80307362	TAATATTGTCGTCTG[-/T/TT]TTTTTTTTTTTTTTT	57674
rs550270616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275941	TGTTGGGATTACAGG[C/T]GTGAGCCACCATGCC	57674
rs550304984	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370533	CGTGAAGACACAGTA[C/G]CTGGAGGTATTGTTT	57674
rs550329051	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80317458	CTAGAAGAGCGCTTC[A/G]GAGTCTTACTGAGAG	57674
rs550341024	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393878	ACCCCTCTTTTTTTT[C/T]TTCTTCTAATTCTGT	57674
rs550350846	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80274645	GTGGGGGGTGTGGGG[G/T]GAGTGTGTGGGGTGA	57674
rs550367580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341234	GTGAGCCACCACGCC[C/T]GGCCTGAAGTTTACT	57674
rs550382306	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80342491	AACTTCTAGTGGATC[-/T]TTATAGATTCTCTTA	57674
rs550417674	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80274343	ACTAGGCGAGGCTTT[C/T]GAGGGGAGCGTCCTG	57674
rs550439607	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356396	ACTCTGCTGTTCACG[C/T]AGCACTAGGCCTGGC	57674
rs550440472	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293840	TAAAAAAAAAAAAAC[A/G]TGTGATAGGGGATTT	57674
rs550447803	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396838	AGGTGGGGGTGTATG[C/T]GAAAGCAACCTGGGG	57674
rs550466628	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338452	TCAATTTTATTATAG[A/G]TTCTTTCTCTAAAGT	57674
rs550476540	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360989	GCTGCACCCCGCCCA[A/C]TAGAAGCCAGATCTT	57674
rs550479826	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305291	TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCCAAG	57674
rs550550708	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80333550	AATACAAAAATTAGC[C/T]GGGTGTGGTGTCAGG	57674
rs550554056	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80305704	GCAATCTCTGCCGCC[A/G]GGGCTCAAGTGATTC	57674
rs550559606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280271	TGGATTCATAGGCCA[C/T]GCGAGGAGAAGAAGG	57674
rs550591990	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397352	AGACCACCCCACATA[C/T]TGTCTTACGCCCAAT	57674
rs550614557	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328227	AACCATCCTAGTCCT[C/T]CTCCTGGTGGCGGGG	57674
rs550615235	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334609	GAGAGTTCCTGCCCA[C/G]AGAGAGGTTTTTTTT	57674
rs550616264	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326948	TCCTAAGTGGTTAAA[C/G]AAAACATGTATAAAA	57674
rs550617559	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80305384	GATTTCTCCATGTTG[A/G]TCAGGCTGGTCTTGA	57674
rs550637506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294649	GTCGTGATCAGCCTT[C/T]TAGGCTAGTGTCTAG	57674
rs550643295	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317550	CCTTCGTTGGACTTG[C/G]GACAGGGATGCTGTG	57674
rs550662132	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340623	GGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	57674
rs550702559	snp	C/G	0.0127313	0.0787626	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355272	AGGTTCGCTTTGGGC[C/G]TACAGCCAGGTGTGA	57674
rs550706352	in-del	-/GTGTGT	0.0011988	0.0244533	intron-variant	RNF213	GRCh38.p7	17:80290365	TGCATGTATGTGTGC[-/GTGTGT]GAGTGCGTGCACGTG	57674
rs550730537	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80262769	CCACCCAGTGCCTCC[A/G]TCCCTCGTTCAGGCC	57674
rs550768460	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390375	CTACTGGGTTTTCTT[C/T]AAGCAATTACACAAG	57674
rs550770177	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320711	AATGTTTTGAAAGAC[C/T]GCTCAGGCTGGACAC	57674
rs550785127	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385715	CCCATCCCTGTCAAC[A/G]CCCAGCACTGTGTTT	57674
rs550791755	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80284552	CCATCTCAAAAAAAG[A/G]AAAAAAAAAAAGCCT	57674
rs550802839	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326176	CAAGTTAGCATGTAG[C/T]AGAGTGATGCCATCA	57674
rs550804883	in-del	-/TGTT	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385726	CAACACCCAGCACTG[-/TGTT]TGTTTGTTTTTGAGA	57674
rs550805243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390966	ACTCAGGAGGCTGAG[A/G]CAGGAGAATTGCTTT	57674
rs550805945	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80293861	TAGGGGATTTGACCT[A/G]GAGGTCGGCAGAAGC	57674
rs550827385	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80284940	GATGATAGACATCAG[C/T]GGTTGACACCAGCCC	57674
rs550845947	snp	G/T	0.000399281	0.0141238	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386303	TTGGATCTGGACACT[G/T]AGTTTGAGATCCTCT	57674
rs550866484	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80302050	AAGAGAAATACTGCA[C/T]ATTCCCACTCATACG	57674
rs550872916	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279945	TTTTGCAGAGGGCGA[C/T]GGCCTCCCTGCCTTC	57674
rs550895440	in-del	-/A	0.317451	0.240729	intron-variant	RNF213	GRCh38.p7	17:80297787	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	57674
rs550910645	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80304588	GAGCTTGCAGTGAGC[C/T]GAGATCACACCACTG	57674
rs550912050	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379862	TAGCAATGCCAAAGT[C/G]CCAGCAGTCACACAG	57674
rs550927007	snp	A/G	1.64784e-05	0.00287035	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288595	GAGTCACCCTGGCCC[A/G]TTTTGTCACCTTGGC	57674
rs550928170	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298169	GGCTGAGGGAAGCCC[C/T]GTCTCCTGCGTGAGT	57674
rs550932462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344416	CACATACATAATACA[C/T]GTATAGCTTAGTGGA	57674
rs550935406	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310476	CAAGCTGGTCTCAAA[C/T]GCCTGACCTCACGTG	57674
rs550939149	snp	A/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80315319	TGGAGGTGATGGTGG[A/T]GGTGGTGATGGTGGA	57674
rs550990266	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388935	CCATGCCTGCTGAAG[C/T]GGGAAGTCCATGGAA	57674
rs550995144	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369205	GCAGTTCGAAACCAG[C/G]CTGGCCAACACGGTG	57674
rs551023712	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80302369	GTATGCATATATATT[A/G]TATCCATATATTTGT	57674
rs551044281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359951	TGCCTGGCCTGTTGG[C/T]CCCTTTGTTTTTGAG	57674
rs551105333	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289266	CGTGAACATTCTGGC[C/G]GCTGTAAGAAGCATC	57674
rs551119119	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398239	ATTTTGGTTTGGTGT[A/G]AACTGTAAAAGTGTG	57674
rs551124511	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283274	CAGGGCCAGGTGGCA[G/T]TTCACACGGGAAGAG	57674
rs551134643	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380441	TCCCGGTTTTTCCTT[C/T]GGGGAGATGAGAACA	57674
rs551165869	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373768	TTGGGAGGCCGAGGC[A/G]GGCGGATCACTTGTG	57674
rs551175441	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374393	CTGGTTCCTGTACCC[A/G]TTCAGACGGTTCTTT	57674
rs551198192	in-del	-/CAAA			intron-variant	RNF213	GRCh38.p7	17:80311195	CCTGTGCCATAAAAG[-/CAAA]CAAACAAACAAAAAA	57674
rs551221351	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338941	CAACAATGCAAGACT[C/T]CATCTCAAAAAAAAA	57674
rs551234677	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80349670	TGGCAACTGCACCGC[A/G]CTGAACATCGCAGGT	57674
rs551251009	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80269503	TCCATCCATTCATCT[A/G]TTCTATCTATCCATC	57674
rs551257967	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391248	TTATATTTATCACCC[A/G]TTTGTATATCATCCT	57674
rs551258825	snp	A/C/G	3.38916e-05	0.00411641	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288225	GGGGACCGGTCCCCC[A/C/G]ACCTCTGCTGGTGAA	57674
rs551297431	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393967	GTACATATATTTCTG[C/G]GTTCCCACGATGATG	57674
rs551299200	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374810	CAGTTGAGCTGGGTT[A/G]ACAGATTTGCTGTGT	57674
rs551314327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269183	ATGCTGCCCACCCAC[A/G]TAGAGGGTGGGTCTT	57674
rs551329430	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394378	CATGTATGAATATCT[A/G]GTCCTTTCTGTGGTT	57674
rs551333627	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320046	TGTTCGTATGCCATA[C/T]GGTACATCTGTCAAA	57674
rs551375934	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358567	AGTGCTGGGTGAAAC[A/G]CAGCCCTCAACTTCA	57674
rs551413073	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363467	TTAAGGACACATCTC[A/G]CTGACGCTTCTCACA	57674
rs551448152	snp	C/T	0.000228938	0.0106966	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80278880	AGCCCCGCTTGAGGC[C/T]GCCAGCGTGCCTTCT	57674
rs551459062	in-del	-/TT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80350232	TATGTTTCCCATCAC[-/TT]TGGGGAATTTTCTTT	57674
rs551460150	in-del	-/AAAATTTTTATAAAATT	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372276	CATATTTTTATATCC[-/AAAATTTTTATAAAATT]AAAATTTTTATAATG	57674
rs551460232	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80283565	CTCTGCCCAACCTCC[A/G]TGTGCTGCTGCTGCT	57674
rs551475786	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272468	CCTGATGGGACATCT[G/T]GACTTCATAACAACC	57674
rs551477219	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349268	GCTGGACGTAGGAAT[C/T]TGAGCTCAGTGGTGA	57674
rs551502934	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383464	TAGTAAGAGAAATAT[A/G]GGTTTCTGAATCTCA	57674
rs551520896	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357658	AAAAATAGTTACATA[A/C]AAAAATTATGCAGCC	57674
rs551527763	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298045	TCAGTCAGGACCCTG[C/T]GTTGACTACTTAGCC	57674
rs551571332	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80297476	AAAGTTGTTTTGGCC[A/G]GGCATTATGGCTCAC	57674
rs551589445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331637	CAGGTGATCCGCCCA[C/T]CTCAGCGTCCCAACG	57674
rs551594071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268301	CAACGCTGCAGTGAG[C/T]CGTGATCATACCACT	57674
rs551628571	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80337475	GAGCCCTGGGGAAGC[A/G]TGGGGAGAAGGCTCT	57674
rs551643540	snp	C/T	0.00262938	0.0361632	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353109	TGGTGGAAGGGCAGA[C/T]GGCAGGTGTGGAGCG	57674
rs551649385	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277265	AGGAGTGGGGAGGAG[A/G]GAGTCATTGCTGTGG	57674
rs551652315	snp	A/G	0.00010767	0.00733643	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363786	GCTGTCATCAGGGAA[A/G]TCAGGTGAGACCCAG	57674
rs551681527	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352689	TCCATGCGTCCTTCC[A/C]ACGCTGGCCATTGCA	57674
rs551696816	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323655	TTTAGTAGTTTCACC[A/G]TATTGGTCAGGGTGG	57674
rs551713004	snp	A/G	0.0185938	0.0946107	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320650	CCACCTTGGCCTCCC[A/G]AAGTGCCGAGATTAC	57674
rs551726071	snp	C/T			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374585	GCATTAAGACTGCTC[C/T]GAAGGTAGGATGGGC	57674
rs551736478	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352000	GCTGGCATTACAGGC[A/G]TGCGCCACCATGCCC	57674
rs551749445	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329223	TTGGCAGAGCACACC[C/G]TCACTGGCTTCCTGA	57674
rs551749611	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80336326	CATTCATGAAGCATC[C/T]GAAAAAGCTGTGGAA	57674
rs551786240	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335848	CAGGCGTGGTGGTGG[G/T]CGCCAGTAATCCCAG	57674
rs551791468	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282057	AGATGGGGTTTTGCC[A/G]TGTTGGCTAGGCTGG	57674
rs551800112	snp	A/G	1.65051e-05	0.00287267	intron-variant	RNF213	GRCh38.p7	17:80313172	AGGAAATTGAGGTAG[A/G]CATTTGGCCGAAGGC	57674
rs551817488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343568	ACAGGCTTTATGGTA[C/T]ACACTGTCGCTCCTA	57674
rs551839991	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303580	TTCTTTTTTTTTTTT[A/T]TTTGAGACAGTCCTG	57674
rs551854435	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387117	ACCTCAGTCCCCCAA[A/G]GAACTGTTGAGGTCT	57674
rs551893574	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379113	AGGAGGATTGCTTGA[A/G]CCTGGGGAGGTCAAG	57674
rs551899274	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301214	TCGTGAAATCTTTGC[C/G]CATTCCTATGTCTAG	57674
rs551926468	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376588	TCACTGGAACACCCC[C/T]CAGAGCTTGTCACTG	57674
rs551933924	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266230	GTAGATCGCTTGAGC[C/G]CAGGAGTTCGAGAGC	57674
rs551939399	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311848	GATCACACACTTGGC[G/T]GGGTGTAGTAGCTCA	57674
rs551953759	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311570	AGCACCTGCATCCTG[G/T]TCCCTCTTACATGCT	57674
rs551956118	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80318131	CACCTGTTTCCAGTG[A/T]AGCTACTTCTCTCTC	57674
rs551959547	in-del	-/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80299806	ACTTACAAGTGAGAA[-/C]CTGCGGTATTTGGTT	57674
rs551983180	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80362045	GTGGGTGAAGGGGTC[A/G]CCCAGTCTCCTCTCA	57674
rs551996744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387907	ATCTACTGTACTTAT[A/G]TACGGTACCACCCGC	57674
rs552004252	snp	A/G	0.00122693	0.0247378	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383027	AAGAAATGAGGAACA[A/G]CTGGGAAAAGGAAAT	57674
rs552020127	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398199	GACCTGACTTGGATA[C/T]CCTGATACTCTGATT	57674
rs552026786	snp	A/G	1.64928e-05	0.00287161	missense	RNF213	GRCh38.p7	17:80347850	ACCGGCTGGAGAAGC[A/G]CTATCTGGATATCAA	57674
rs552030620	in-del	-/TA	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80302487	TGCATTTGTATACAT[-/TA]TGTATTGTATACATA	57674
rs552043107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282463	GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA	57674
rs552052189	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80332726	TTTGAAAAGGGGGGC[A/G]GATGACTTAGAGCTT	57674
rs552116412	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80290430	GTGTGTGCGAGTGTG[C/T]GCGTGTGTGCATGTG	57674
rs552122732	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391073	TCTCAAAAACAAACA[A/G]AAAAAAGAATAGAAA	57674
rs552128800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317609	TGTGGGAGGGAGCAC[A/G]TGAGTGAGTGTGGCA	57674
rs552154220	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296239	TGGCCAGGCTGGTTT[C/T]GAACTCCTGACCTCA	57674
rs552154591	in-del	-/TTTTTTG	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80340795	CTGGCTAATTTATTT[-/TTTTTTG]TTTTTTGTTTTTTGT	57674
rs552191595	snp	A/G	0.000152069	0.00871846	missense	RNF213	GRCh38.p7	17:80346973	CCCCACAAAAAGGTC[A/G]GCTTCGTGGGCATCT	57674
rs552200759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322705	AAGGCATGAGCCACC[A/G]CACCTGGCCTCTTTT	57674
rs552227366	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286711	GAGTGGGCACAGGTT[C/T]ACACCTGCTGCCTGG	57674
rs552292342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317984	TGGAGAGGGGAGCTG[A/G]AGAGGGGATGGGTCA	57674
rs552306553	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80293958	AGAGCTGGGGTGGGC[A/G]GGCCTGCCAGTCTAG	57674
rs552339692	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296921	CCTGACCTTGTGATC[C/T]GCCTGCCTCGACCTC	57674
rs552366754	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381884	GAGAGAAAACCGTGT[C/G]TAGGGAAGGCGATGC	57674
rs552383588	snp	A/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80280842	AGAAATGGATGGGAG[A/T]TTTATAGTAAAGCTG	57674
rs552385009	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80348408	AGGGAGATGCTGAGA[C/T]GCTGAGCTCTCCTCC	57674
rs552396155	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285935	CCTGCCTCGGCCTCC[C/G]AAAGTGCTAGGATTA	57674
rs552429331	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290157	GTGGGCAGGGAGTGG[C/G]CACCTCTTCTTCCTC	57674
rs552447092	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352004	GCATTACAGGCGTGC[A/G]CCACCATGCCCAGCT	57674
rs552447356	snp	C/G	0.00398564	0.0444627	intron-variant	RNF213	GRCh38.p7	17:80323335	GAGTCCTCCTACTTT[C/G]TTCTTATTTTTCAAG	57674
rs552482957	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396338	ATGAGACTTTGTGCA[C/T]GTGTTAACCGAGACG	57674
rs552489273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294509	TGGGACGTCTAGGAT[A/G]TCTGTTTGCACGGGG	57674
rs552510987	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305646	AGACAGAGTCTCACT[C/G]TGTTGCCCAGGCTGG	57674
rs552512068	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285611	TGATACCTGCTGATG[A/G]CGCCACTCTACAGTG	57674
rs552514557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276540	CAAGAGAAAACCGAC[A/G]TGAACAAGAGAACAA	57674
rs552516550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271010	GATGCTTCCATACTT[C/T]TTGCTGGTTGGCCCT	57674
rs552520799	snp	C/T			missense	RNF213	GRCh38.p7	17:80345882	CTCTGGCTGAGGACT[C/T]TGGCCTGCATATTAT	57674
rs552536066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374923	AAGAAAGATGCTGAC[A/G]CAACTATTAATAGCA	57674
rs552557362	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321710	CTGGTGGGTATGAAG[A/T]GGTATCTCCTTGTGG	57674
rs552570799	snp	C/T	0.000494372	0.0157144	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374508	GTACCTGGTGTACGG[C/T]GATGAATACAAGGCT	57674
rs552594848	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365415	CCCCGGAGGCTGGCA[C/T]GGAGTCAGGTGCCCA	57674
rs552607069	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80293920	GAACTAAACAGTTGC[A/G]GGCCCTGCTGGGCCC	57674
rs552623337	snp	C/T	0.00325671	0.0402213	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363832	GCTTCATCTGGCGCG[C/T]GCTCACCAGGAGCCT	57674
rs552677395	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298926	GGAGGTTGCAGTGAG[C/G]TGGGATCATGCTACT	57674
rs552677507	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293010	TGGACAAAGACAGAA[A/G]TCCTAAGAACTTTAT	57674
rs552682204	snp	A/T	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304614	CACTGCACTCCAGCC[A/T]AGGCAACAGAGTGAG	57674
rs552698846	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377672	TCATATTGTGGTCAG[A/G]GCCAGAGAGTAGAGA	57674
rs552706302	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396331	AATAGTTATGAGACT[C/T]TGTGCATGTGTTAAC	57674
rs552710282	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354310	TGGGAATCTAAGAGC[A/G]TCTCTCAGATTTTGC	57674
rs552713122	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380583	CTTAACACCCTGCCC[A/G]GGGATCAGCATCAAT	57674
rs552753697	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263216	CAGTAGCCCTGGGCT[C/G]CCTGCTCAGGCCCCA	57674
rs552788159	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327636	TGGGCAAGACCTAAC[A/C]CTCGTGGGGGAAAGC	57674
rs552795184	snp	A/C	0	0	intron-variant	RNF213	GRCh38.p7	17:80334551	CCTTAAAATCTTGCC[A/C]CCTTCAGCTTTTTCT	57674
rs552806084	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380011	TGTAGAAATATGCAT[A/G]ACATAAACAGATGAT	57674
rs552835817	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80340501	GGTGTCAATCAGGGT[C/T]TGTGCCAGAACCAGG	57674
rs552840546	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273563	CTTCTGCACCTGATT[C/G]ATCTCTGGCTGGAGT	57674
rs552845654	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80349054	GATGGAACCGAGAGA[C/T]ACTCAGGAGGCAATT	57674
rs552852898	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273156	GGGTGAATCTCTCCA[C/T]GCACTCGTGGGGAGG	57674
rs552853051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279018	GTCCCTGCCAGTCGA[A/G]GAAGGCTGCCCAGGA	57674
rs552921423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384372	GCCGGCGGTGCTGGG[A/G]TACTGGGGAGCAGTC	57674
rs552929533	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80344486	CTGGCTCAGAACGCA[A/G]CTCCCACAGCAATGC	57674
rs552961219	snp	A/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80269413	TCCTATCATCTATCC[A/T]TCCATCCATCCATTC	57674
rs552991791	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80350589	GAAAAGGCCAATAAC[A/G]TTACAAAAATAGTGG	57674
rs553003306	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266622	TGTTCCTGCCTCAGC[C/T]TCCCAAGTAGCGGGG	57674
rs553043904	snp	A/C	3.61788e-05	0.00425301	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288017	CCCCAGGCACAGCCA[A/C]CACGCCACTGGAGGG	57674
rs553047550	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353793	TGAGGATGGCGCCCC[A/G]CTTTCCTCACACAGT	57674
rs553073077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333215	AACCACGCCCGGCTA[A/G]TTTTTTTGGTATTTT	57674
rs553086263	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358713	CAAGAGATCAAGACC[A/G]TCCTGGCCAACGTGG	57674
rs553109727	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80339262	ACTCTGCTGGGAATA[C/T]GCTGTTCAGGACGTG	57674
rs553109860	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332596	AGCCTGGGACTGAAC[A/G]GTGACTTCAGTGTTC	57674
rs553119594	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80324841	GGACACTTAAGGAGG[C/T]AGTATACAAGGAAAT	57674
rs553124940	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384837	TCCCTCTTCGCCGCC[C/T]TCCATTTCTAGCACA	57674
rs553163626	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389453	GAGCATTCAGGGAGT[A/G]CCACTCTAGGCGCTC	57674
rs553218137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316044	TATGGAGATAATGGT[A/G]GTGGTGGAGGTGATA	57674
rs553218391	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320107	ACAGATATGTACAGT[C/G]ATCACCACAGTTAAT	57674
rs553231217	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365860	AGGGCCAGGTGCCCA[C/T]AAACCCAAAGGTAAA	57674
rs553257981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337233	CAGAGGGTTCTCTGC[A/G]TTGGGGACCTGGCAG	57674
rs553270026	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80309569	CTCCCAAAAAATACA[C/T]GTCCAAACATGGTCT	57674
rs553289696	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299312	TTTCGTTTTTTCAGC[A/G]TGCTTTCATAAGCAT	57674
rs553317947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267570	CATTCCCTTAAACCA[C/T]AGCCGAATCCACAGT	57674
rs553321001	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325400	TAATGCTAACAGCCA[C/G]TATTCATTGAATGCT	57674
rs553350644	in-del	-/A	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80267230	TCAAAAAAAAAAAAG[-/A]AAAAAAAAGAGACCA	57674
rs553386904	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80318852	TGCTGGGATGACAGG[C/T]GTGAGCCACCGCGCC	57674
rs553416115	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291911	GCGTCTCTCTGGAGA[G/T]CACAGACTTTGCCTG	57674
rs553429843	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342752	ATATATATTGTATGT[A/T]TATATATATTATATA	57674
rs553449039	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352789	TGGGTGGTTTCTGCG[C/T]AGGCCCATTCCAGGG	57674
rs553455073	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319757	TATTTAGCTCTTTTC[A/G]GCAAAGGGGAAGAGA	57674
rs553507735	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397686	ACTCGGGGAGCTCAG[C/T]TGTTGGAGACATGAG	57674
rs553518869	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387991	TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGGC	57674
rs553536486	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394566	CTCTGGACTAATTTC[C/T]CTTCCTAGACAGCTC	57674
rs553549258	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307832	TGGGATTACAGGCGT[C/G]AGCCACCATGCCTGG	57674
rs553564802	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296344	TGCTTTTTGAAGCTT[C/T]GTGTGGTATCATGAG	57674
rs553587708	snp	A/G	7.31663e-05	0.00604796	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373175	CAGCAGGTGAGAAGC[A/G]GGGCCGGGCAGCACA	57674
rs553602531	snp	C/T	0.00016616	0.00911331	synonymous-codon	RNF213	GRCh38.p7	17:80347992	CTCTGACGTCTTCAT[C/T]GGCTACCACTCGGAC	57674
rs553623846	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318635	CTGGAGTGCAGTGGC[A/G]GGATCTCGGCTCACT	57674
rs553633856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391895	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	57674
rs553643132	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398416	AGACTATGGAGTACT[A/C]TGACACCAGGAAAAC	57674
rs553675168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322979	TGAAGATTTACTCCT[A/G]TGTTTATTTATCTCT	57674
rs553681639	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393064	CTCGCTGTAGCCTCC[A/C]CCTCCTGGACTCAAG	57674
rs553697342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366255	TAGTTGTTTTGGATA[C/T]GTACCTTGAAGGGGA	57674
rs553724968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388509	ATACACAGGGCAGCG[C/T]GGCACTACGCTGCAG	57674
rs553732720	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377424	TTAAAGTTGTTATAA[A/G]ATATGCTCATGACAA	57674
rs553748092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373951	GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG	57674
rs553786680	snp	C/T	6.66267e-05	0.00577139	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383670	TTTTTTCATTTTCTC[C/T]ATCCAGCATCTAGAT	57674
rs553810871	snp	C/T	1.65026e-05	0.00287246	synonymous-codon	RNF213	GRCh38.p7	17:80348229	CAACTCCTTTGCAGA[C/T]TTCCTTCAGGCACAC	57674
rs553818390	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286957	CCTGCTGAGGGTGCG[A/G]TGGGAGCTGCTACTC	57674
rs553839007	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80274297	TTAGACACCAAGAGA[A/G]TGCGTCCTTGTTAAG	57674
rs553841918	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80271699	TTGAAAAAGAAAAGG[A/C]CGGGTGTGGTGGCTC	57674
rs553853695	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353244	GGGCCGAGCAGGTGC[A/G]CTTACCACAGGCTGA	57674
rs553862468	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378080	AGTCCCTGGATGCCA[A/G]GAGCACCCACTCCTC	57674
rs553905008	snp	C/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80271077	GCCCTGATTGGATTA[C/G]GCTAGTCAGGGCCCG	57674
rs553905647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277377	CTGAGGCGGGTGGAT[C/T]ACTTGAGGTCAGGAG	57674
rs553927390	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80336975	AGGGTCTGAATTGAC[A/G]TACGCAGCTTAACTA	57674
rs553941575	snp	C/T	0.000148499	0.00861553	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381648	CAAGATGCTGGGACA[C/T]AGTGCCGACGAGACC	57674
rs554034409	in-del	-/T	0.166746	0.23573	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351665	TAAAATAGGTATTCT[-/T]TTTTTTTTTCTTTAA	57674
rs554039886	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391874	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	57674
rs554058246	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259819	TGTTCCCATGGCTGT[C/T]GTGGGCAGTTGTCGG	57674
rs554067269	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386951	GTGAACAAGCAGCCC[C/T]TGGTGTGTTTCTCGA	57674
rs554104895	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374869	CGCCTTTTGATTTAT[A/G]CCCATTACTTCCTTT	57674
rs554120841	in-del	-/CTCACTGCAACCTTGG	0.0352571	0.128006	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390467	TCACTGCAACCTTGG[-/CTCACTGCAACCTTGG]CTCACTGCAACCTCT	57674
rs554189421	snp	A/G	4.95733e-05	0.00497837	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351821	GAGATCAGAACATCA[A/G]TCAGGGTATTTATTT	57674
rs554201303	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329488	AAGCTCTTGAGCTCT[C/T]TCTGTTACTCATATT	57674
rs554210586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362594	AAATAGCCAGGCCAC[A/G]CGGCTGACAGTGTAG	57674
rs554220750	snp	A/G	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80285745	GCGTAATATCGGCTG[A/G]CCGCAGCCTCTGCCT	57674
rs554244080	snp	C/T	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80335432	CTCTCTTGGGAGAGC[C/T]GCTGCTTTCAGTGGT	57674
rs554250661	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341503	CTTTTATTAGCTAGT[C/T]ACTCAACACATAATG	57674
rs554268992	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259294	CCAACATGGAGAAAC[C/T]CCGTCTCTACTAAAA	57674
rs554275006	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335971	GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA	57674
rs554291079	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365823	TGCACAGGGCTTTCA[G/T]CCAGGTCCAGCGTGG	57674
rs554300870	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351443	TTCAAAGCAGAGGAC[A/C]CAGGAATGGGGAAGA	57674
rs554307185	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80286168	CCAGGTGCTCTCAGC[A/G]GTGTGGTGGGTTGGT	57674
rs554311949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341986	TAGTTTTTAGTAGAG[A/G]TGGGGTTTCACCATG	57674
rs554314500	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334727	TGCCTCCCGGGTTCA[C/T]GCCATTCTCTTGCCT	57674
rs554332109	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265986	GGACATGGGAAGCCC[A/G]TGGCCAGGCTGGAGA	57674
rs554343779	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80311343	GCCCGTGTCAGGCTC[C/T]GGAGGTCTGTGCAGC	57674
rs554376730	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386533	TTCCCTAACAGACAC[A/T]CACTCCTTCAGCCGC	57674
rs554405983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318076	TTCCGAAGTTAAACC[A/G]TCTCTCCTTGGAAGT	57674
rs554420318	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80298990	CTAAAACAAACAAAC[-/A]AAAAAACTATCAAGA	57674
rs554442661	snp	C/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80322317	AGGCATGTGCCACCA[C/T]GTTCAGCTAATTAAA	57674
rs554448043	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275291	GGAGCACATGGGATG[C/G]GGAAGGTTTGGGTAA	57674
rs554463255	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80331638	AGGTGATCCGCCCAT[C/G]TCAGCGTCCCAACGT	57674
rs554464121	snp	A/G	0.000119469	0.00772789	missense	RNF213	GRCh38.p7	17:80340302	CTGTCGGCGGCAGCC[A/G]TGTTCAATGACCGGC	57674
rs554489287	in-del	-/GT	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80274714	GGGTGAGTGGGGTGA[-/GT]GTGGGGGGTGAGTGG	57674
rs554489925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310500	TCACGTGATCCACCT[A/G]CCTTGGCCTCCCAGA	57674
rs554495593	in-del	-/GG			intron-variant	RNF213	GRCh38.p7	17:80274966	GGGGGTGTGTGTGTT[-/GG]GGGGTGTGTGTGTTG	57674
rs554505572	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289981	GGGGAAAAGGGGACC[A/G]CTTAGGAGGTGGAGG	57674
rs554521486	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80294466	GGCCCGCTGCATCCC[A/G]TGACCCTGGGCTTTC	57674
rs554526411	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80309691	GATGGCAGGATGACC[C/T]GGCTCCTCCGTCCCA	57674
rs554566995	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80294238	TGCCAAGGGCCATCT[A/G]TGCCAGCTGGGCAGC	57674
rs554580444	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320440	TCACCGCAACCGCTG[C/T]CTCCCGGGTTCAAGT	57674
rs554597353	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80327393	TGTTCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG	57674
rs554620590	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300115	AATGGTATTTGTGGA[A/G]TTGCCACACTGTCTT	57674
rs554698519	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396417	AGAAACAAACTTCCA[C/G]TGATAAATATTGGGA	57674
rs554700273	snp	G/T	0.00057682	0.0169728	intron-variant	RNF213	GRCh38.p7	17:80307103	TCAATCTTTTGTCCT[G/T]TTTTTCTTTTTTTCT	57674
rs554711600	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362595	AATAGCCAGGCCACG[C/T]GGCTGACAGTGTAGC	57674
rs554714868	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321281	ATTTGTATGTTGAAT[C/T]TTTCACTTGTGGCAT	57674
rs554724497	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317330	AGGCAAGCTGGAGAA[C/T]CCCAGACCATTAGCG	57674
rs554724927	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385812	CTGCAACCTCTGCCT[C/T]CCGGATTCAAGCAAT	57674
rs554752149	snp	A/G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397709	GACATGAGTCTTGCC[A/G/T]AAGCGCCCGGCTGAA	57674
rs554759614	snp	A/G	1.8627e-05	0.00305175	intron-variant	RNF213	GRCh38.p7	17:80350432	TCAGAAACTATGTAA[A/G]AAACCCAAAACGTAG	57674
rs554760630	snp	A/G	1.66664e-05	0.00288668	splice-donor-variant	RNF213	GRCh38.p7	17:80298519	ACAAATGCTAGATAC[A/G]TAAGTCGTAGAGTTG	57674
rs554796573	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299090	TCCAAATATGGATTC[A/G]TGGGTGTTTTATGTA	57674
rs554807013	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80304802	CACTGCTGTGTAGCC[A/G]TCAGCACCATCCACC	57674
rs554817529	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320119	AGTCATCACCACAGT[A/T]AATGACAGAGCATTT	57674
rs554817571	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80326470	TATTGATAACACTGT[G/T]ATTAACTAAAGTCCA	57674
rs554832723	snp	A/G	0.000115081	0.00758469	missense	RNF213	GRCh38.p7	17:80334247	GAAAGGAGTTCATCT[A/G]CTGGGTCCGGGAGGC	57674
rs554882287	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292551	GAGATGACATCCAGA[C/G]CCCCGTCTGCAGGCT	57674
rs554896742	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357329	TGTAGTTAACCAATT[A/G]TCTTTCTGTCTGCCT	57674
rs554920464	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298849	CCAGGTGTGGTGGCA[C/T]GTGCTTGTAATCCCA	57674
rs554921342	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80279622	GGCACCTGCCACCAC[A/G]CCCGGCTACTTTTTT	57674
rs554923859	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286291	CGGAGGGTCGGGGGG[C/T]GGGGGCGCCTCCTGT	57674
rs554934352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303816	CTCAAGTGATCTGCC[C/T]GCCTCAGCCTTCCAA	57674
rs554943358	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289288	AGAAGCATCCCCTGT[A/T]GGGGTCAATGTGGAG	57674
rs554959669	snp	C/T	0.000280216	0.0118334	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354452	ACAGCCTCTTTCTTG[C/T]GGGTATCCAAGATGC	57674
rs554998089	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80323833	CTAAGTACTTTTTTT[-/G]TGGGGGGGGGTGCTA	57674
rs555004363	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80293590	GCATTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	57674
rs555026859	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387303	GTAGAGATGGGGCTT[C/T]ACCACGTTGCCCGGC	57674
rs555058826	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380650	TCGGGTCTGGTCCAC[C/T]GGAAAGGCGAGTCTA	57674
rs555061229	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80306094	GTCAGCCTCCCAAGT[A/G]TTGGGATTCAGGTGT	57674
rs555064482	snp	C/T	3.33829e-05	0.00408538	intron-variant	RNF213	GRCh38.p7	17:80349955	CTCCCCAGCCGCAGC[C/T]GTGTGGCTTCTGCGT	57674
rs555073677	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304337	TGATCCTGGACACTC[A/G]TTAATAATAATTAAG	57674
rs555103664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279552	TCACTGCAACCTCCG[C/T]GTGCAGGGTTCAAGC	57674
rs555114708	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282805	AGGTTCAAGTGATTT[A/C]TCCTGCCTCAGCCTC	57674
rs555154203	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368732	GTGACCACACCTGGC[C/T]GACGCCACTGGTTTT	57674
rs555166839	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80277073	ACAAAGCAAACAAAC[-/A]CAAAAAAAAAACAAA	57674
rs555192874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273525	CCATTGAACCTGCCC[A/G]CAGGGCAGCAGCAGA	57674
rs555217083	snp	A/C/T	1.6507e-05	0.00287284	missense, synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368141	TGTTTCCCAAGCGCA[A/C/T]AGGTACAACACCCTT	57674
rs555239840	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353472	CAGTCCCTGTGCCAC[C/T]TTCTGAGTGGTAACG	57674
rs555241316	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375575	GCCGGACATGGTTGC[A/G]TGTGCCTGTAGTCCC	57674
rs555268234	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80313610	GGTGGTGGTGGAGGT[A/G]ATGGTGATTGTGGTG	57674
rs555272957	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395238	ACTGGCCTAGCAGAG[G/T]CAAAAAAAAAAAAAA	57674
rs555296162	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359578	GGGAGGGAGACAGAA[A/G]GAAGAAAGAGAAAGA	57674
rs555308536	snp	A/T	1.67027e-05	0.00288982	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388593	TAATTTTAAAAAACT[A/T]TTTTCTTTCCCAATT	57674
rs555372277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272727	TGGCAGAGTGGGTGC[C/T]CCATGCTGTCTGCAT	57674
rs555377481	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272948	TGCGCTGACATCCTA[C/G]TACAGAGTCAGGTGA	57674
rs555422355	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80338523	GTGCAGTGGCTCACA[C/T]CTGTAAAGCCAGCAC	57674
rs555453400	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262060	CTGGTCTGTGGTTCC[C/T]CAGTGTAGCATTGGA	57674
rs555461798	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80269333	ATATTAACCATCACA[A/C]CGTCTATCCATCCCT	57674
rs555483395	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363005	ATGGTTTCTAATTTC[C/G]TCTTTTATGGTTTTC	57674
rs555499766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342151	CAGCTCCCCACTGTA[C/T]GTAGGATGCCCCCAT	57674
rs555499872	snp	C/G	1.65119e-05	0.00287327	missense	RNF213	GRCh38.p7	17:80347910	TCGTGGAGGAGCTCT[C/G]TGCGTGGGTGGAGAA	57674
rs555521563	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80330168	TTAAATTCTGTCCTG[G/T]TCTTGTTCACGTTGC	57674
rs555524530	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268740	CTATCCTATCTATCC[A/G]TCTATCTATAAGTCT	57674
rs555575882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271744	AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	57674
rs555607397	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393562	TCTCCTCGTCTGCGG[C/T]GTGGACTTGATCATG	57674
rs555614537	in-del	-/TTTT/TTTTT	0.156176	0.240966	intron-variant	RNF213	GRCh38.p7	17:80305184	CACCCAGCAGTGAAC[-/TTTT/TTTTT]TTTTTTTTTTTTTGA	57674
rs555632252	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80278301	CAGGGCCAGACTGCC[C/T]GCCTCCGCCTCTAGG	57674
rs555635961	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310040	TTACAGGCTTAAACC[A/G]CCACGCCCAGCCTCC	57674
rs555664784	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353763	GCTAGAGGAGTCGCC[A/G]CCGCTGTGCAGGGGT	57674
rs555670707	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326694	TTCACTTAGTAATAC[A/G]TATTTATGTTTCCTC	57674
rs555677714	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80306918	ATTCTTCCTTTCACA[-/T]TTTTTGGTGGAGAAA	57674
rs555695513	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348932	ATGGAGCGGGCACTG[G/T]AGGCACGCTTGTCTC	57674
rs555730526	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348346	AGTCCTAAATCCCTC[G/T]TGTCAGGATTCAAGA	57674
rs555780127	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337169	TTGGGGACCACAGAA[A/G]GACACTGAGGACTTG	57674
rs555849498	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392486	TCCGTGGGCTTCTGT[C/T]GTGTTTGTGTACTGC	57674
rs555851634	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357218	CCGTGCCCAGCCACC[G/T]TTTAATTCTTATCCT	57674
rs555867098	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324694	TATGCTATATTAAGG[G/T]TTTATTCATTTTTGG	57674
rs555874591	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291896	CCCGCGGTACTGGAC[A/G]CGTCTCTCTGGAGAG	57674
rs555882303	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318596	TTTTTTTTTTTGAGA[C/T]GGGGTCTCGCTCTAT	57674
rs555911704	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80350713	CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG	57674
rs555943206	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312355	GAAGAGGGGTTTTCC[C/T]TCTGGTCTGGTGGGT	57674
rs555960668	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300665	TTCAAGTGATTGTCC[A/T]GCCTCAGTCTTCTGG	57674
rs555964191	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277362	CAGCACATTGGGAGG[C/T]TGAGGCGGGTGGATC	57674
rs555968684	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307959	ATTTTTCCCTTACTT[A/G]TAAATAGTCATGATA	57674
rs555979531	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80307704	ACAGGCGCATGCCAC[C/T]ACGCCTGGCTAATTT	57674
rs555984332	snp	C/T			missense	RNF213	GRCh38.p7	17:80345852	TCCTGTGTGATCATA[C/T]GGTGGATGGCCAGCC	57674
rs555984474	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80276914	AAAAAAAAATTAGCT[G/T]GGCGTGGTGGCGTAT	57674
rs555984528	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384469	CATTTTCTACAACAC[A/G]TTGTCTAAACATTTC	57674
rs556009794	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80322430	AAATACAAACAATTA[A/G]CTGGGCATGGTGGCA	57674
rs556013715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329282	CGAATCCTTGTGTGT[C/T]TAAAGATGTCTGTCC	57674
rs556014794	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352397	CGGCGTGGAGACTCC[C/T]GACTCCCGACAGACA	57674
rs556020444	snp	A/G	3.50244e-05	0.00418461	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383107	CTGGGTTGCTCCTCG[A/G]TCCAGAAAGGAAGGG	57674
rs556030841	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369303	CTTGGGAGGCTGAGG[A/C]AGGAGGATCACTTGA	57674
rs556048697	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272237	TGCAGTGAGCCAAGA[C/T]TGTGCCTCTGCACTC	57674
rs556077880	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80342514	TTCTCTTACTCTTTG[A/T]CCTAGCCCTGGGACT	57674
rs556085278	in-del	-/TCTG	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80298971	GCGACAGAGCGAGAC[-/TCTG]TCTAAAACAAACAAA	57674
rs556097590	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80281010	GTGTGGAAAGTGGGG[C/T]GTCTAGACCATGGGC	57674
rs556127653	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381895	GTGTCTAGGGAAGGC[A/G]ATGCCTGGGGCTGGA	57674
rs556132234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306022	TAAAGTAGAGACAGG[A/G]CCTCACTAGGTTCCC	57674
rs556133698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335321	GTCGTTGGCAGAGGA[A/G]AGAGGAAGAGGCAGA	57674
rs556147821	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80337234	AGAGGGTTCTCTGCA[C/T]TGGGGACCTGGCAGA	57674
rs556159356	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382204	AAAAAAAAAAAGCTA[C/T]AAAATATTGTATTCA	57674
rs556177903	in-del	-/TTG	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375996	TAGAGGTTCTCAACC[-/TTG]TTATGTGGAGGAACA	57674
rs556194342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387605	TAACTGGTGCCCACC[C/T]CCAGGTTCTTCAGTC	57674
rs556200707	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361664	CCCCTTCACTCCGGA[A/G]CCCCCTGGAGGCAGG	57674
rs556209250	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397591	CCCAGTCACGTACCC[C/T]CTGCTTGCTCAATCA	57674
rs556216253	in-del	-/AAGAG			intron-variant	RNF213	GRCh38.p7	17:80351320	AGACCCCCATCGCTT[-/AAGAG]AAAAGAAGGAATGGA	57674
rs556256962	snp	A/G	0.0115144	0.0749975	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387942	GGGCCAGGAACTGTG[A/G]GAGCCCATGGATTTT	57674
rs556266767	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356282	GCTGGGATTCCAGGC[A/G]TGAGCCAGTGTGCCC	57674
rs556313896	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285141	TGATGGGGGCCTTGC[A/G]TGTACCAGGCAGTGT	57674
rs556315588	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275076	GAGTTGGGGGTGTGT[G/T]AGTGGGGTGTGTTGG	57674
rs556370942	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80269658	TCTATTCATCCATCA[A/G]TCTATCCATCCATCC	57674
rs556396268	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80310622	CAATGGCGTGATCTC[C/G]GCTCACCACAACCTC	57674
rs556402516	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386500	CCAGTGGGGCAGACA[A/C]AAGCAAGCTTCAGCC	57674
rs556407499	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80331879	CTCTTCCTGAGAAAG[A/C]AATCCTAGCAGCTGT	57674
rs556417398	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80262874	CTGCTGAAGGCACCA[-/G]GTCAGCTGCCGCTCC	57674
rs556442963	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396353	TGTGTTAACCGAGAC[A/G]GCCCTGAGCTATTTC	57674
rs556445132	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360523	AGAGGAGGACTGTCG[C/T]CTCTATCAGCTGGTC	57674
rs556446238	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285718	CTCTATTGCTCAGGC[A/T]GGAGTGCAGTTGCGT	57674
rs556447896	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392015	TCAAGTGATCTGCCC[C/G]TCTCGGCCTCCCAAA	57674
rs556455090	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80348103	TGAGGAGGCCAAATC[A/G]ATCCTGCTGAACTGC	57674
rs556474007	in-del	-/TGC	0.00716266	0.059414	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382150	ACCATCACAGTTGTG[-/TGC]TGATTTATTAAATGT	57674
rs556511038	snp	A/G	1.64754e-05	0.00287009	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376258	AGAGCAATTCACACA[A/G]TATTCTTTGATACAT	57674
rs556511342	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80333643	AGGTTGCAGTGAACC[A/G]AGATCGTGCCACTGC	57674
rs556513891	snp	C/T	1.65831e-05	0.00287945	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369833	AAGACTCCTGTCATC[C/T]GCTCAGTGATACTGA	57674
rs556538652	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361136	TGTAGCCATGCAACA[C/T]ACAACTCAGTCTTAT	57674
rs556540710	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366158	CCTTCCGCCGTGAGG[C/T]TGGCTCCCTCGGCCG	57674
rs556556651	snp	A/T	0.000148661	0.00862023	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369452	AGTCATTCTGTAAGG[A/T]GGCATTTGGGAAACA	57674
rs556599652	snp	A/G	8.32064e-05	0.00644952	missense	RNF213	GRCh38.p7	17:80346910	AAAATGCCCCTGAAG[A/G]CTCTGCACCCGCTGC	57674
rs556606500	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356041	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	57674
rs556607179	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80334816	TGTTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	57674
rs556619158	snp	A/G	5.7076e-05	0.00534179	intron-variant	RNF213	GRCh38.p7	17:80289857	GGATGCCCCCGCAGG[A/G]GAGCAAAGGAGACCC	57674
rs556646787	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370880	CAATGTTGGTTGGTG[A/G]TGATAACATTCAAGC	57674
rs556650299	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80300316	GTCACCCAGGCTGGA[A/G]TGCAGTGGTGTGATC	57674
rs556652754	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271063	CAGGGTAAATATCGG[C/T]CCTGATTGGATTAGG	57674
rs556682148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364661	TCTTTTGGCTCTGAC[C/T]GTTTTGTCTAGACAT	57674
rs556684128	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289521	CTTGAGCCTGGGAGG[C/T]GGAGGTTGCAGTGAG	57674
rs556684841	snp	C/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355513	GGGGTGACCGGGAAT[C/G]GGGGCTTACAGGGGG	57674
rs556698877	snp	A/C/G/T	8.23862e-05	0.00641777	synonymous-codon	RNF213	GRCh38.p7	17:80349880	GCAGCAGTTTGACAC[A/C/G/T]GAGTACTCATTCCTC	57674
rs556728988	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300585	TTGAGATGGAGTTTC[A/G]CTTTATCACCCAGGC	57674
rs556748194	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80264283	TGAGGCTCTGCAGGG[G/T]TTGAGAGCTCTGCCT	57674
rs556771130	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80292210	CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	57674
rs556775345	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80271849	GCTGGGTGTGGTGGC[G/T]CATGCCTGTAATCCC	57674
rs556845297	snp	C/T	0.000872722	0.020871	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367979	TGGGATTCAGCCGTG[C/T]TCCATCTGCCTGGGA	57674
rs556857982	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269446	CTATTCTATCTATCC[A/C]TCCATCTATTCATCC	57674
rs556872937	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80293695	CGGGCGTCTTGGCAG[C/T]GGGCGCCTGTAGTCC	57674
rs556894157	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317011	AGAAAGCCAACCTGG[C/G]CTGCTGTGACCGGCC	57674
rs556901461	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80299000	ACAAACAAAAAACTA[G/T]CAAGAATACAGAAAC	57674
rs556904681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380075	AAAACCTGGGCATCC[A/G]TCTGTCTCAGCAGAT	57674
rs556958074	in-del	-/TCTC	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80281884	TTTTTTGAGACGGAT[-/TCTC]TCTCTTTTGCCCAGG	57674
rs557007756	in-del	-/CAGTGGTGTCCAGCAACAGTGGCCACT	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365109	CCCTCTGTGGCCACG[-/CAGTGGTGTCCAGCAACAGTGGCCACT]CAGCCAAACACAGCC	57674
rs557024573	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80350557	GTGGGATTAGGGAAA[C/T]TGAAGAGAGACAAAA	57674
rs557041667	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80283461	CTCTCCTGCAGTTGC[A/G]TCTGCGCTTACTGCA	57674
rs557045351	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395934	TTTCCGCCATGGATG[C/T]CTCATCACCAACCCT	57674
rs557060326	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354386	GGACAGAAGCACTCC[A/G]GAGCCAACAGCTCAG	57674
rs557079974	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358770	AAAAATTAGCTGGGC[A/G]TGGTGGCGCGTGCCT	57674
rs557106455	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319811	ACAGTCTCGCAGGCA[A/G]TGCCACATGAGGAAG	57674
rs557109167	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380621	AGCGCAGCCACCTGA[C/T]GCTGAGAATGCGGTC	57674
rs557141497	in-del	-/GT	0.0502198	0.150293	intron-variant	RNF213	GRCh38.p7	17:80290489	TGTGTGTGCGCACGT[-/GT]GTGTGTGCGCGTGTG	57674
rs557148060	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381252	GAGTAGAGAGGCTGA[C/T]ATCTTCATTATTTTA	57674
rs557170493	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375052	GTTTTTAGAATCTAA[C/T]CTTTAAATTGGTCTG	57674
rs557187919	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80304496	ATACAAAAAATGAGC[C/T]GGGCGTGGTGGCAGG	57674
rs557190123	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296853	CTTCCAGCTAATTTT[C/T]GTATTTATTGTAGAG	57674
rs557197533	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80325444	CGACTGTGCTGGGTC[A/G]CAAGGGAAGTGCCCT	57674
rs557211177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392905	TAGGATTTTAAGTCT[C/T]AACGAGCATTTTGGT	57674
rs557220395	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385277	AGGAGGCGCTGATGG[C/G]TGCTCTATAGCCTAA	57674
rs557234280	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80331859	GGGAGGGAAAGACCT[A/G]TGAACTCTTCCTGAG	57674
rs557234480	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80266320	AGAATTAGCTGGAGC[A/C]GGAGGATCACTTGAG	57674
rs557235446	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388888	ATTGACATCTTGTGG[C/G]TTTGATTCTTAGGAA	57674
rs557267117	snp	C/T	0.000362629	0.0134604	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363161	GGCGTCAGAAGCGCC[C/T]GAGGAAGAGGTTTCC	57674
rs557284665	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394700	ACAAAATGCTTGTCC[A/G]GGACTCAGCCATGCA	57674
rs557292421	snp	A/C	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80297791	GACTCCGTCTCAAAA[A/C]AAAAAAAAAAAAAAT	57674
rs557308326	snp	C/T	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80282499	CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT	57674
rs557314865	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320112	TATGTACAGTCATCA[C/T]CACAGTTAATGACAG	57674
rs557324906	snp	A/G	0.0115144	0.0749975	intron-variant	RNF213	GRCh38.p7	17:80304619	CACTCCAGCCAAGGC[A/G]ACAGAGTGAGACTCC	57674
rs557324997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363912	GGGAGGGGCTCCGTC[C/T]TCACCCGTTCACTCC	57674
rs557365179	snp	C/T	0.000494201	0.0157117	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369547	GCAGATGTGCAACAG[C/T]TTCTTCGTAGACCTG	57674
rs557394559	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394252	GACATTTTGAAATTG[C/T]GAGAGAAACTAGATG	57674
rs557407109	snp	A/G	0.000116672	0.00763689	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363642	GCAATGGCCTGCACG[A/G]AGATGCTGACAAGAA	57674
rs557427023	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385255	GGAACAGGGTGGGGC[A/G]GAGGGGAGGAGGCGC	57674
rs557470025	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80308952	AGGAGCTAGTCATCA[A/G]TGGTAACCATTTTCT	57674
rs557491823	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389553	ACAGTAGAGACAGAC[A/G]CGCGCTAGAAATGCC	57674
rs557502662	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287504	GAGACCTTGTCTCAA[A/G]TAAATAAATAAATAC	57674
rs557554060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303790	GGCCAGGCTGGTCTT[A/G]AACTCCTGGCCTCAA	57674
rs557570680	snp	A/T	0.000115453	0.00759693	missense	RNF213	GRCh38.p7	17:80337614	GGAACTTGGAATGGC[A/T]GAAGACTGTGAATGA	57674
rs557592175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343402	GCGTGACTCCTCCCC[A/G]TGTATAGAATTCCTT	57674
rs557607522	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373985	TCCAGCGCCTGGGCG[A/T]TAGAGCGAGACTCCG	57674
rs557618218	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80268611	CATCCATCTGTTTGT[C/T]CATCCATCCATCCAT	57674
rs557628461	snp	A/G	1.64887e-05	0.00287125	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393494	GGAATCGAGAAATGA[A/G]ATAGAATTATTTCCT	57674
rs557654236	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261957	GGGAGGCGGAGGTTG[A/C]AGTGAGCTGAGATTG	57674
rs557690121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296461	AATGTTCTCCCCATG[C/T]CCCTGCCTGTGCCGT	57674
rs557702457	in-del	-/TC/TCTC/TCTCTC	0.561782	0.144487	intron-variant	RNF213	GRCh38.p7	17:80342540	GACTTAATTTTTCTC[-/TC/TCTC/TCTCTC]TCTCTCTCTCTCTCT	57674
rs557706596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366328	GCACTGTATTGTTTT[C/T]CACGGGGGCTGCAGC	57674
rs557727108	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384153	ATACACACCCACGTT[A/G]GGATTAGCAGTGACC	57674
rs557747414	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372229	TAACAGTGGTTATCA[C/T]TGAGTGGGGACATTA	57674
rs557788719	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379483	GGTTCTCCACCCACC[C/G]GAAACAAGCACACAC	57674
rs557831967	snp	C/T	3.29522e-05	0.00405894	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369589	TTGCTTCAAGGACAA[C/T]GCTCCGCCTGAGAAG	57674
rs557843046	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268159	AGTAGTGTTCCATTA[C/T]GTATATGTACCACAT	57674
rs557869910	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366935	AGTGATGATGTGTAT[C/T]GCCTAAAAACCAGTG	57674
rs557889568	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80301584	AATGCAAATCAAAAC[C/T]ACAATGAGATATGGT	57674
rs557895309	snp	G/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395477	TTCACATGTGAGACG[G/T]TGGACTTTTCCTCTG	57674
rs557898096	in-del	-/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352874	GGTGTGCAATGTCCC[-/T]GCTTAGGGCTGAGCA	57674
rs557899431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362893	AGTTCATGATGTCAT[A/G]TTCAGTGGCAAAAAG	57674
rs557990250	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259879	ACTAATTGTTGGCGA[A/C]CCCCCGCCCCAAGCA	57674
rs557992483	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398467	GACTGGCCAGCATTA[A/G]AGGTAGGTTGGCCAT	57674
rs558053073	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80306658	AGATCGAGACCATCC[A/T]GGCTAACACAGTGAA	57674
rs558059263	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358205	TTTGTTAATGCTCAA[G/T]AAGGAACAAAATGTC	57674
rs558060490	snp	C/T	4.95364e-05	0.00497652	synonymous-codon	RNF213	GRCh38.p7	17:80348163	CGCCTACTCGCTGGG[C/T]GGGTTCGCAGCGGAG	57674
rs558072157	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353419	GGGAAGCCTGCACTC[A/G]GAGGCTGAGCACACA	57674
rs558080502	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80277395	TTGAGGTCAGGAGTT[C/T]AAGACCAACCTGACC	57674
rs558116345	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286750	GGCCCTCATCACACA[C/T]CACCAGGTTTCAGGG	57674
rs558142856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342044	CCTTGAGTGATCACC[C/T]GCCTCAGCCTCCCAA	57674
rs558151320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378016	ACGTGGCTCTGCGGC[A/G]TGGGCTGTCCTGTGC	57674
rs558182451	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351579	ACCGAACCAACAGCT[C/T]GGAGAACACCCTTCT	57674
rs558190315	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260316	GGGGCGCGCCTGTCC[C/T]GCCCCACTCGGCTGC	57674
rs558224774	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396952	ACAGCCCATAAAAAA[C/T]GCCTTCAGCCCTGCT	57674
rs558230133	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351902	GCTCTGTCACCAGGC[C/T]GGAGTGCAGTGGCGC	57674
rs558233423	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371635	GTTCTCAATTTTTAA[A/G]ACTATAAAGGGGTCC	57674
rs558249446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267399	AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	57674
rs558257007	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322376	GGCTCATGCCTGTAG[A/C]CCATCCTGGCTAACA	57674
rs558267042	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356543	CCACTGTGTTCTGGG[G/T]ACTGGAGTCCTTTGC	57674
rs558280466	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297069	GTACAGAGTTAGTGC[C/T]GGGGCTTAAAGTATG	57674
rs558283018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336726	ATAATTGATAGAATT[C/T]TTTATCAGAAAAAAG	57674
rs558308796	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80306776	AGAATGGTGTGAACC[C/T]GGGAGGCGGAGCTTG	57674
rs558360365	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381972	TTCCCTCCATTCACC[C/T]CTGCCTGGCTAAGAC	57674
rs558361856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312282	AGGAGGAAGGAGAGG[A/G]AGGAAGAGGAAGGCA	57674
rs558376932	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80308582	TGTCCATGTGTCCCT[C/G]AGAAAACACAAAACC	57674
rs558398734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311691	CCCACTCTCGGGCAG[C/T]CCCGCCCAGCAGCAG	57674
rs558428487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300210	CCTCACCAGCATCTG[C/T]TATTTTTTTACCTTT	57674
rs558431262	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80334771	AGCTGGGACTACAGG[C/T]GACCGCCACCACGCC	57674
rs558473311	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353234	TAGAGCACCAGGGCC[A/G]AGCAGGTGCGCTTAC	57674
rs558482642	in-del	-/TGG	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80313442	GGTGATGGTGATGGT[-/TGG]TGGTGGTGGTGGTGG	57674
rs558496200	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305959	TCTGTACTTTTCATT[G/T]GATTCACTGCATATT	57674
rs558505398	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310555	ACTGCACCCAGCACA[A/G]TTTTTTTTTTTTTTG	57674
rs558513670	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329268	AGAGGTTAAACCCTC[A/G]AATCCTTGTGTGTCT	57674
rs558520473	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80298599	GAGTCCCGGTGGGCT[C/G]TGCAGTGACTCCATT	57674
rs558528237	snp	A/C/T	3.29485e-05	0.00405874	missense, synonymous-codon	RNF213	GRCh38.p7	17:80307170	AACATTTTAGAAATG[A/C/T]TGTTGCGACTCCTGG	57674
rs558552892	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384653	GCTTAGATCCTAGGT[C/G]TTCGGAAGGACACCC	57674
rs558583597	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80340485	GTGTGATTCATCTGT[A/G]GGTGTCAATCAGGGT	57674
rs558602141	snp	A/G	0.00193363	0.0310334	intron-variant	RNF213	GRCh38.p7	17:80340368	GTTGGTAAGGAGAGC[A/G]GCAGGGTGGGCAGGC	57674
rs558636577	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318178	TCTTTATAGGCACAA[C/G]ATAGGGGGCAGGGTG	57674
rs558649045	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80336837	ACCCGGGAGGCAGAG[A/G]TAGCAGTGAACTGAG	57674
rs558683184	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391991	CAGGCTGGTCTCGAT[A/C]TCCTGACCTCAAGTG	57674
rs558698459	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80297173	AAGTTGTTTTGGGGC[C/T]GGGCACGGTGGCTCA	57674
rs558720112	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392390	TTTTGAATGGTGAGG[A/C]CTTGTTTATGCAACC	57674
rs558741196	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80299824	GCGGTATTTGGTTCT[C/T]GTTCCTGAGTTAATT	57674
rs558779880	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328026	ACTTCAGGCTCCTGA[A/G]GCATTAAGTAGCTGG	57674
rs558804197	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351370	CACCCTTAGCTGCAC[C/T]GGGGCAGGCCCATTG	57674
rs558820796	snp	A/G	6.58903e-05	0.00573941	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389951	TCTCTGCTGGACAGA[A/G]GGACTGCGCTCCCTT	57674
rs558820863	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395864	CATGCTGGCCTGCAC[C/T]GGAAGACTCACTTTG	57674
rs558837531	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396545	CATAAAGTGTGAAGG[C/T]TGCATAACTGGGGAG	57674
rs558848337	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80318546	GCTCAAGGAAAATTA[C/G]TTTTTATGTGATATG	57674
rs558855957	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390709	AGCCTAAAAGTCATA[C/T]ATTCTAATTTTATAA	57674
rs558872131	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80350526	TAACAATTCTTCCCC[C/G/T]GCCTCATTCCCCCAA	57674
rs558873180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327220	AAATATACTCAGGCC[A/G]TGTGAGGTGGTTCAT	57674
rs558875706	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290335	TTCACGTGTGTGTGC[A/G]CACGTGTGTGCGTGT	57674
rs558883663	snp	C/T	0.0107246	0.0724382	intron-variant	RNF213	GRCh38.p7	17:80311032	GGCTGCTATTTAAAC[C/T]GCCACAGGCAGCTGC	57674
rs558898532	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80316253	CGAGACCCTGTCTCT[C/T]AAAATATTTTTTTTA	57674
rs558936713	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320790	GACAAGCCTGGGTAA[A/C]AGAGTAAGACCCTGT	57674
rs558948397	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298266	GACTCCAGACTCCCA[G/T]GGAGATGACTCCCTG	57674
rs558949997	snp	C/G/T	0.000209071	0.0102225	intron-variant	RNF213	GRCh38.p7	17:80340404	CTCCCAGGGACTGCC[C/G/T]GGGGCCCTTCCCCCC	57674
rs558965612	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285028	CCGATAACAGGGAGA[G/T]CCAAGGGACCATTCC	57674
rs559008289	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390409	TTTTCAGACAAGAGT[C/T]TTGCCCTGTTACCCA	57674
rs559008424	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394362	TCTCAGTGTGCTCTC[A/G]CATGTATGAATATCT	57674
rs559042362	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394743	CGCCGGCAGGAGGCA[C/T]GGAAGGAACTGTGCT	57674
rs559046601	snp	A/C/T	1.64754e-05	0.00287009	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375774	GGCCTGCAAGACCCC[A/C/T]CAAAGCCAGCAGTCA	57674
rs559059689	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289451	AAAAATTAGCCAGCC[A/G]TGGTGGCATGTGCCT	57674
rs559094405	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320447	AACCGCTGCCTCCCG[C/G]GTTCAAGTGATTCTC	57674
rs559097345	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274466	CTTGCTGGGCACGGA[A/G]AAGGGGAAGCTGTCT	57674
rs559113329	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379535	ACGTCTGCCGGTGAT[A/G]AGGAGGTGTTCATTT	57674
rs559116557	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364276	GCGAGAGCTGGGGGC[A/G]GGCCAGGAAGTATGT	57674
rs559119815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262209	ACGGTGGGAGCCAGG[A/G]CTTGGCTGTGGCAGG	57674
rs559132837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326557	CCACCATTCCAGTAT[C/T]GTGCAGAATAGTTGC	57674
rs559143871	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80299109	GTGTTTTATGTACTT[A/T]AAAGAACAACAACAA	57674
rs559147240	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80326170	GTTGCGCAAGTTAGC[A/G]TGTAGTAGAGTGATG	57674
rs559168460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359644	GAAAGAGTGAGAGAA[A/G]GAAAGAAATGGAATT	57674
rs559175214	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374181	CCACCCGGCCTCAGG[G/T]GTGGTGCGGTGCGCC	57674
rs559229501	in-del	-/CA	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381492	CTCTACCAGGCTCAC[-/CA]TCTTCTCTACAAACC	57674
rs559231970	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363989	TGGAGACACGAGAGG[C/T]GGCTGTGCATTCAGG	57674
rs559259338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298004	TTTACTGTTGCCAGA[C/T]GGCCTGGGTTCAAAC	57674
rs559287376	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80350026	GTGACTGTGAAATAG[A/C]TCCTTGTTAAATCTC	57674
rs559303074	in-del	-/T	0.0886606	0.19097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392989	GTTATATGGGAGCCT[-/T]TTTTTTTTGAGACAG	57674
rs559326415	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341656	CTTGGGAGGATCGCT[C/T]CAGCCCAAGAGGTCG	57674
rs559328796	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355102	GGTGCTCTGGGCCCC[A/G]GACAGAGGGTCTCTT	57674
rs559390038	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378350	AACTGTTGATTATTC[C/G]TCTCTGGATTCCCAA	57674
rs559402706	snp	C/T	0.000115532	0.0075995	missense	RNF213	GRCh38.p7	17:80344014	GGAGCTCTTCAGCGC[C/T]GGTCTGTACTGTGGG	57674
rs559405836	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325684	TGATTTCCCCCCAGC[C/G]CCCCGCGCCCCAGGT	57674
rs559425312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303877	CTGTGCCTGGCCAGC[C/T]GTTGGGAACCAATTC	57674
rs559428078	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332053	CAAGACCTCAGCAGT[A/G]AAAGATTAAATGACA	57674
rs559438324	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80264650	ACATGCAGAGGGCCC[C/T]GCTGGTCTCCCCGCC	57674
rs559446649	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288541	GCCCACCCTGTCCCT[C/T]GGCTTGTGGCAGATG	57674
rs559455641	snp	A/C	2.8333e-05	0.00376374	splice-acceptor-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353510	GTTTGCTTCGACTGC[A/C]GTGGGCTTGGAACAC	57674
rs559461602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277446	CTACTAAAAATACAA[A/G]AAGTAGCCGGGTGTG	57674
rs559462216	snp	A/G	0.000232458	0.0107784	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353074	CGTGAGTCACGAGGC[A/G]GAGCCCCTGGGGGAG	57674
rs559465341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272810	GCCTTAGTGCCAGGA[C/T]AAGGGAAGCAGTTTG	57674
rs559497903	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80303552	TTCTATTCCTTTTCT[C/T]TTTTCTTTTCTTTTC	57674
rs559501648	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283281	AGGTGGCAGTTCACA[C/T]GGGAAGAGCTGAGGG	57674
rs559506478	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361972	GAGACGTTTCCTCAG[C/T]TGCCTGGAGCTGGTG	57674
rs559516834	snp	G/T			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321794	AGTGGCGTGATCTTG[G/T]CTCACTGCGACACCT	57674
rs559529712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388433	CCGCTGGATTCCCGG[C/T]TGTGTTACTATTTCC	57674
rs559544034	in-del	-/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80283567	TGCCCAACCTCCGTG[-/C]TGCTGCTGCTGCTGT	57674
rs559552051	in-del	-/AA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359551	AAAAAAAAAAAAAAA[-/AA]GAGTGAGAGAGGGAG	57674
rs559555765	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260054	ACGGAGGTCCCTGGT[C/T]ACACCATGAGCCTCA	57674
rs559563758	snp	G/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80316855	GTTGAATGAATGTGG[G/T]TGGTGGTGTGCTATT	57674
rs559566623	in-del	-/A	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355821	GGAATGGGGGCTTAC[-/A]GGAGAAGAAGCGGGG	57674
rs559573658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272423	GGCAGAGTAGGCCGA[C/T]GGGGATGCTGACAGC	57674
rs559595763	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383453	AGCCAGAATGTTAGT[A/T]AGAGAAATATAGGTT	57674
rs559633540	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80282869	CGCCTGGCTAATTTT[C/T]GTATTTTTAGTAGAG	57674
rs559642783	snp	A/G	0.00438332	0.0466095	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261080	GCCCGGTCCAGCCCC[A/G]CCCGCGGCGCCCACT	57674
rs559650500	snp	A/C			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319857	GGCTGCCCTGCTCAC[A/C]TTTCCTAATTGGACA	57674
rs559655297	in-del	-/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80275066	GTTGGTGTGTGAGTT[-/G]GGGGTGTGTGAGTGG	57674
rs559662448	snp	A/G	0.000345006	0.0131295	intron-variant	RNF213	GRCh38.p7	17:80337802	GTCTTCTGGCCCCAA[A/G]AAAGTGACTTCTAAC	57674
rs559681294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291135	ATTTTTATCCAGTGA[A/G]TTGATGACATTCTTC	57674
rs559730039	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373843	GTCTCTACTTCAAAG[-/A]AAAAAAAAAATTAGC	57674
rs559736866	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360579	TGGGGCACTGGACTC[A/G]GAAGATGCCCCCAGG	57674
rs559740886	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393608	ATTCAGAAGGAGAGC[C/T]GTCAGCGTAGCACCG	57674
rs559787096	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348477	TGAGTGCCTGGCTCT[G/T]TGCAGTGCACCATGC	57674
rs559796330	snp	G/T	0.000114175	0.00755476	missense	RNF213	GRCh38.p7	17:80336301	CTGGACCCCAGCGTG[G/T]ACTTCAGTGCATTCA	57674
rs559833076	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80342234	GTGTGGTCGGCTCTA[C/T]CATCTGGGTTTCTGC	57674
rs559835847	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80313720	TGGTGATGGAGGTGG[A/T]GGTGGTGGAGGTGAC	57674
rs559860672	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271342	TTGAGCTCTTGGCTA[C/T]GCCAACACTGAGTAC	57674
rs559874824	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80343074	CGGCCTCCCAAAGTG[C/T]TAGGATTACAGGTGT	57674
rs559883536	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367193	GTTTTAAAACATTCA[A/G]AATAATAACTCCATG	57674
rs559893923	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80297681	AGTCCCAGCTACTCG[C/G]GAGGCTGAGGCAGGA	57674
rs559904857	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80318323	GGGTTTCAGGCTTTT[C/T]GGCTCGAAGGTGGGG	57674
rs559943498	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80317925	GGACACTTGAAGGAT[A/G]GTGAAGGTGGAGAAT	57674
rs559943593	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322546	GTGCCACTGCACTCC[A/G]GCCTGGGCGACAGAG	57674
rs559961200	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324273	TCCTTTTTGTTCCTC[A/G]TTTGTTGAATGCTTT	57674
rs559966254	in-del	-/TG			intron-variant	RNF213	GRCh38.p7	17:80290460	GTGTGTGCGAGTGCA[-/TG]TGTGTGTGCACGTGT	57674
rs559970168	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370755	CGGCTGCTGTGTTCA[C/T]GGACCGCCACCCGTG	57674
rs559989637	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296866	TTTGTATTTATTGTA[C/G]AGACGGGGTTTCACC	57674
rs559997159	snp	C/G	0.0023933	0.0345097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374368	CTTTAAACCTCGAAT[C/G]ATCAACCACCTGGTT	57674
rs560001112	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80330256	CATCATGTGCTGCTT[C/T]CTCCAGGTTCCTTTC	57674
rs560008176	snp	C/T	0.000249945	0.0111763	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372777	TGGGTTTAAAGACTC[C/T]GTTATTTAGAAATTC	57674
rs560041648	snp	A/G	0.00557542	0.0525036	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362560	TTAAAAACAACAGCC[A/G]CCGGCCAGTGCTGCA	57674
rs560047150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392047	TGCTAGGATTACAGG[C/T]GTGAGCCACTGCGCC	57674
rs560072411	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392931	TTGGTTCTGCTGATG[A/G]CAACGGGAAAAAGTA	57674
rs560093707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307274	TGACCCCTATAATTG[A/G]CCGTGACCCACATGT	57674
rs560117182	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300345	TCTCAGCTCACTGCA[A/G]CCTCTGCCTCCTCGG	57674
rs560139475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311811	CACTTGCACGATGTG[C/T]GGGGCTGTGCTTAAA	57674
rs560153712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276981	AGAATCACTTGAACC[C/T]GGGAGGGGGAGGTTT	57674
rs560178504	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80322019	GTGAGCCACTGTGCC[C/T]GGCCTCATTGTGGTT	57674
rs560187103	snp	A/G	8.23608e-05	0.00641667	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377821	GGTATTTAAGATAGG[A/G]TTTGAGGGGTGGCGT	57674
rs560189035	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301183	GCTTTTCTTGTGATT[G/T]CTTTTGGTATTTTTG	57674
rs560196288	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271834	ATACAAAAAAAATTA[G/T]CTGGGTGTGGTGGCG	57674
rs560217319	snp	A/C	0.00517822	0.0506191	intron-variant	RNF213	GRCh38.p7	17:80334575	TTTTTCTTCCAGTAG[A/C]TTTTTACTGGAGGAC	57674
rs560219953	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377041	TGAAGCATTGGGTTC[A/G/T]ACTTGGGGTCCACGT	57674
rs560223423	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351995	AAGTAGCTGGCATTA[C/T]AGGCGTGCGCCACCA	57674
rs560233717	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397099	CTTCCTCAGAACCCA[C/T]GATCTTTGCCCCATC	57674
rs560234620	snp	C/G/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80290646	CCATTCAATCCTGAC[C/G/T]TCCATAAAGTCTTCA	57674
rs560249299	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286371	AAAATCGGAATTTCT[C/G]GCCCTGGTTCTGGCA	57674
rs560253467	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301751	AAGAAACTAAAAATA[C/G]AACTACTGTATGATC	57674
rs560267510	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351567	GGTGGCCGTGAGACC[A/G]AACCAACAGCTCGGA	57674
rs560273182	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365395	CCAAGGCTAAGGTAC[C/T]AGCTCCCCGGAGGCT	57674
rs560282041	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311540	CAGCCCCCTCTGCGG[C/G]CTCTCTTTCACAGCA	57674
rs560305465	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80371011	TTAATGAATATGGAT[A/T]TTTTTTTTTAAAACG	57674
rs560308642	snp	A/C	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80290577	TCCACCAGCACGCTG[A/C]GCCCGGGTGGAGGAG	57674
rs560310063	snp	A/G	3.30502e-05	0.00406497	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375888	GAGTAACCGCCTGCA[A/G]GGCTGTGTTCAAAGT	57674
rs560345611	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280809	AATTGGTGAGGATAC[G/T]TAACAGATGTGAGGA	57674
rs560346987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381156	TCCCCCTGTGGCGTA[C/T]GATGGTATGGGGGGA	57674
rs560377715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299946	TATGTACCACATTTT[C/T]TTTATCCAGTCTACT	57674
rs560398778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356276	CGAAGTGCTGGGATT[C/T]CAGGCGTGAGCCAGT	57674
rs560400750	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361204	GACCTAAATTTGACA[C/T]TGTTTCCGCCTTCCT	57674
rs560407712	snp	C/T	0.0498117	0.149749	intron-variant	RNF213	GRCh38.p7	17:80290414	GTGCTTGTGTGTGTG[C/T]GTGTGTGCGAGTGTG	57674
rs560456161	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382072	TCAGCCCCGTAGGTC[A/G]TTCCCCTACCATGCT	57674
rs560457184	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80305619	CCTTTTTTCTTTCCT[G/T]TTTTTTTTTTGAGAC	57674
rs560488089	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80304214	ACTTCTGTTACTTCT[A/G]GGGAGCCTTGCTTTA	57674
rs560498338	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284838	TCCTCTGGTGATTGA[G/T]TCCTCTGGAGAGAGG	57674
rs560507994	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265063	TTTTTTTTTTTTTTA[C/G]AGGGAGTTTTTTTGT	57674
rs560558137	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364975	TTTGGGGTCTTCAAA[A/T]CAGTGCTGTCAACAG	57674
rs560559669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359798	AGACTTGGTTCTGCC[C/T]GAGATTTTGGGCAAC	57674
rs560569960	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284329	AGATCATGCCATTGC[A/C]CTCCAGCCTGGGCAA	57674
rs560577357	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80285428	TCGCCTCTCCGAGGG[A/G]AGGCTGTCTTCAGGG	57674
rs560585066	in-del	-/TGTCATGT	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377609	TAAGCTTCAGGCAGG[-/TGTCATGT]AACTTAACAAATTAG	57674
rs560598714	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80327333	TGAGACCCTGTTCTC[C/T]ACAAAAAATTTTGAA	57674
rs560602175	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352080	AGATGGTCTCAATCC[A/G]TTGACCTCATGATCC	57674
rs560618848	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360793	AGCCATCTTTCATAC[A/G]TGCAATAGTCTTTTC	57674
rs560623390	snp	A/G	0.00597247	0.0543191	intron-variant	RNF213	GRCh38.p7	17:80270369	GGCCGTCTGGAGGAC[A/G]GATTCCCAGCCACTA	57674
rs560655344	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391478	GGGTTTCTCCACGTG[A/G]CCAGGCTGGTCTCGA	57674
rs560702280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270071	ACACTGTAAACTGGT[A/G]TGTCCTCTTCTAGAC	57674
rs560714602	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80269368	CCTATCTGTCCACCT[A/G]CCCTATCTATCTATC	57674
rs560721325	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307035	ACAATGTATACCATA[C/T]TGATGTTGGATTTTT	57674
rs560775537	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305222	TTGGTCTCATTGCCT[A/G]TGCTGGAGTACAATG	57674
rs560785363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262901	CTCCAGCCACTGCCC[C/T]AGTGGAGTTCTTTGG	57674
rs560813710	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390856	TCACCTGAGGTCAGG[A/G]GTTCAAGACCAGCCT	57674
rs560815990	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350601	AACATTACAAAAATA[C/G]TGGAATGGGCCTGGG	57674
rs560820171	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80334531	AAATGGCTCAGGTTC[A/C]TTTTCCTTAAAATCT	57674
rs560828477	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80270797	ACGTGCTGGGTCACC[A/G]TTGCCCAAGTCCAGG	57674
rs560873261	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351515	GAAGAAATCACGATC[A/G]CAGGGCTCTGAAGTT	57674
rs560892702	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364357	CGCATCTCTTCTCCC[A/G]TCTCCCTCCTCGTTT	57674
rs560894977	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80258958	CCCGCAGAAAAATCA[C/T]GCAAGCCACCAACGT	57674
rs560896581	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359350	GGGCAACATAGTGAG[A/C]CCCCATCACTACAAA	57674
rs560924780	snp	A/G			missense	RNF213	GRCh38.p7	17:80345660	GGCGTGGTGGTACCA[A/G]TGCTGACACCATAAA	57674
rs560928383	snp	A/C/T			intron-variant	RNF213	GRCh38.p7	17:80317452	CTGTCCCTAGAAGAG[A/C/T]GCTTCGGAGTCTTAC	57674
rs560960699	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382342	AGTGATTTTCTTTTG[C/T]TAATCTGCAAAAATC	57674
rs560972024	in-del	-/TCCG	0.0962929	0.197165	intron-variant	RNF213	GRCh38.p7	17:80268634	CCATCCATCCATCCA[-/TCCG]TTTATCTGTCTATCT	57674
rs560977175	snp	C/T	0.000164014	0.00905428	synonymous-codon	RNF213	GRCh38.p7	17:80317220	GGAAATCCAATTCCC[C/T]GCGGAGCATGGCTGG	57674
rs561009106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326781	TGTATGGATGTGCTA[C/T]CATTCGCTTACCCGT	57674
rs561031555	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380310	TGTTCCCTGCAGTCA[A/C]AGCTTAAAATACTTT	57674
rs561058461	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293744	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG	57674
rs561062142	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338021	GCATCTTTGCAGTGG[C/T]GCTAAGCTGGTGGTG	57674
rs561064089	snp	C/T	0.000592895	0.0172074	missense	RNF213	GRCh38.p7	17:80344691	AGCGTACACGTGTAC[C/T]CCAGTTCAGTTTTCT	57674
rs561067580	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350082	ATCTTCTGCAACGCG[G/T]TGTCTGGCCTAACAT	57674
rs561074829	in-del	-/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396861	CCTGGGGCCAAAGCA[-/G]GGGGGAAGCAGGAGA	57674
rs561120492	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374264	TCCCTGCACTTGCAC[C/T]TCTTCGTCTACTGAG	57674
rs561122134	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80297354	ACTCAGGAGGCTGAG[A/G]CAGGAGAATCACGTG	57674
rs561122627	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309787	TTAAGACGGGGTCTC[A/C]CTCTGTCACCCAGGC	57674
rs561148699	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394915	CTGCCACCGAGATCT[A/G]CATTCCGACTGCCTA	57674
rs561162038	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369142	GGTGGCTCACGCCTG[C/T]AATCCCAGCACTCTG	57674
rs561167973	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383129	AAGGAAGGGTCCCGG[C/T]GTCTGCTGAATGCTC	57674
rs561178418	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80332747	CTTAGAGCTTCCGTC[A/G]GGGGCTCCTGTGTGT	57674
rs561214217	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269465	ATCTATTCATCCATC[C/T]ATTCATCTATTCTAT	57674
rs561226751	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273796	AGCTAATTTTTTTGT[A/C]TTTAGTAGAGACGGG	57674
rs561261054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380253	TCTAAATGCTCCTTT[C/T]AGAGAGTGAGTGGGA	57674
rs561278582	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390734	TTATAACAAGTAGAC[C/T]ATGTCAAAGAGAGGT	57674
rs561279699	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288493	TGCTCCCTGGGTGGG[A/C]GTCGGAGGGCTGCCC	57674
rs561297840	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379802	AAAGTGATACTCAAG[A/G]TAGTACTAATTACTC	57674
rs561332272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304513	GGCGTGGTGGCAGGC[A/G]CCTGTAGTCACAGCT	57674
rs561338829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297905	GAGGTTATAATGATC[A/G]CACCACCGCGCTGCC	57674
rs561349545	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303437	GACTGGGGACAGCAG[A/G]AAAAATGAGGCAGTT	57674
rs561419263	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283090	TACTTCTAAGCCTCA[C/G]CCCCCGTAAAATTAT	57674
rs561432866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325000	AATGAAAAACTTCTA[A/G]ATGTCCCTCTTTTAT	57674
rs561435693	snp	A/G	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80315078	ATGGTGGTGGTGAAG[A/G]TGATGGTGGAGGTAA	57674
rs561436947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358840	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	57674
rs561485283	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330536	GGTCCTCCCATGGCC[C/T]GTGTTCTCAGTGTGG	57674
rs561486760	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394311	TGGCAGTTCTTTGCG[A/G]ACTTTTTTCTAGCAT	57674
rs561503095	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326390	TCTGCCACCATCACA[C/T]GGGCAGTACCCTGTT	57674
rs561520824	snp	A/G	4.9458e-05	0.00497258	missense	RNF213	GRCh38.p7	17:80291782	AAGAAGGGCGAGTAC[A/G]TCAACCGCTGTCTGT	57674
rs561531462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297360	GAGGCTGAGGCAGGA[A/G]AATCACGTGAACCCA	57674
rs561533903	snp	A/C/G			intron-variant	RNF213	GRCh38.p7	17:80338057	TCGTCCGTGAGGGCT[A/C/G]TGTACTCCCAAGAAA	57674
rs561542144	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278562	GTCTGCAGGAGCTGC[C/T]TCTTCGTCTTCCCAC	57674
rs561542370	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307892	AAAGGGAAATAATAG[A/G]TATCAGCTGCTAAGA	57674
rs561544391	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378288	AGGAGGTGTGGTCCA[A/G]ATGCCAAAGGAAAAA	57674
rs561582575	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307450	CTCACTACAACTTCT[A/G]TCTCCTGGTTCAAGT	57674
rs561598712	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316207	CAGTGAGCTATGACT[A/G]TGCCACTGCACTCCA	57674
rs561607784	snp	A/G	0	0	intron-variant	RNF213	GRCh38.p7	17:80283515	GGGCAGAGGGAGTGA[A/G]GCCAGGCCTGGCTCC	57674
rs561611282	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378989	GACTGGCCCGGGCAA[C/T]ATGTTGAAACCCCGT	57674
rs561615455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80302496	ATACATTATGTATTG[C/T]ATACATATATAGAAA	57674
rs561635236	snp	C/T	0.00181067	0.0300342	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389189	ACTCCCTCCCCAGCT[C/T]GGTCATTAGTGCCAT	57674
rs561647045	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393823	TAGCTCAGCCACACA[C/T]GCAGTAATGACCTGT	57674
rs561647294	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80264998	CATGGGGTCTCTCCG[A/G]TGTTGTCCTTCAAGG	57674
rs561665232	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359053	GCGAACAGCCCCACA[A/G]TCTGTGCTCCTTACC	57674
rs561692960	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261202	GAGGCTTTGCGCCCC[A/G]GCAGTGCTGCCCCCG	57674
rs561734209	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80327653	TCGTGGGGGAAAGCA[A/G]AAGGGAGTGGAATGA	57674
rs561755433	snp	A/G	0.00103941	0.0227733	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361921	GGCTAAGGGTCAGGT[A/G]TAGAGCTTGCATGAT	57674
rs561763712	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286505	GGTGGGTGGGAACGC[A/C]GCCTCCTCCTTGGGC	57674
rs561780536	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261561	CCTGCCCCCACCTTG[C/T]TGACTTTGGTTGTGG	57674
rs561810522	snp	A/C	1.65263e-05	0.00287452	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363278	CCACAGCCTGATGGA[A/C]GCCCGTTGGAACCAT	57674
rs561817341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382893	CGAGTGTTATTTCTA[C/T]TAAACACTTATTTAG	57674
rs561823725	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282307	CTGTTTTCTTCCCCA[A/G]TATTTTCTGTCTGTG	57674
rs561851258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292067	TTACCTACTCACTTG[C/T]AGGAGGAAACATGCA	57674
rs561913526	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395254	CAAAAAAAAAAAAAA[A/T]GAATTTTATTTTACT	57674
rs561929653	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365867	GGTGCCCATAAACCC[A/C]AAGGTAAAGGAGCTG	57674
rs561935681	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80301390	GAAGAGACAGTCCAC[A/G]GAATGGGAGAAAATA	57674
rs561939481	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80347788	CCGCCTGATTGTCAT[C/T]GAAGAGAAAGACGTC	57674
rs561963797	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80267756	TGCTGGAGAAGCTGC[A/G]GTAAGTTCTCCAGAT	57674
rs561971659	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80266098	TTGCAGCTGGTAGAG[G/T]TAGGAAGGCCTCTGA	57674
rs561993090	in-del	-/AT	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80283564	CTCTGCCCAACCTCC[-/AT]GTGTGCTGCTGCTGC	57674
rs561994916	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80342892	CTCACTACAACCTCC[A/G]CCTCCCGGGTTCAAG	57674
rs562023376	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365478	TTCAGCTTCCACCCC[A/G]TGGCCTGGCGTCACA	57674
rs562073083	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80334530	TAAATGGCTCAGGTT[C/G]CTTTTCCTTAAAATC	57674
rs562089186	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389505	GAACAACTGCTCACC[C/G]AGTCAGTCCAGCATA	57674
rs562090413	snp	C/T	0.00874735	0.0655527	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361415	GTCCCAGCTACTTGG[C/T]AGGCTGAGGCAGGAG	57674
rs562112504	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351947	ACAACCTCAATCTCC[G/T]GGGTTCAAGCGATTC	57674
rs562113850	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323281	CCACACTGTTTGGAC[G/T]ACCATTGCTTTCTAG	57674
rs562114737	snp	A/C/T	6.61205e-05	0.00574948	synonymous-codon	RNF213	GRCh38.p7	17:80346456	ATATCGGAAAGCCAT[A/C/T]GCCAGGTTCTTTCCG	57674
rs562129522	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291099	TTACAGGCATGAGCC[A/C]CTGCGCCCAGCCTTT	57674
rs562138156	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318889	ATATGTAACTGTTAA[A/G]TGGATCTTTAAAGGG	57674
rs562202795	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393152	TGCCCAGCTAATTTT[C/T]GTATTTTTGCTAGAG	57674
rs562249809	in-del	-/ATGCTG	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80348665	AATATCATATGATAA[-/ATGCTG]TGCTTAGAGGCAGCG	57674
rs562259797	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259420	TGCAGTGAGCCAAGA[G/T]CACGCCACTGCACTC	57674
rs562273966	snp	A/G	4.95593e-05	0.00497767	intron-variant	RNF213	GRCh38.p7	17:80290735	CTACACCAGGTGAGC[A/G]TGTCTGTAGGCTTGG	57674
rs562293251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372267	TTTTTATCTTCATAT[C/T]TTTATATCCAAAATT	57674
rs562320461	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275542	AATGCTCGAGCAGGA[C/T]GCACTCGAAAAAGAC	57674
rs562333036	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293249	TATTTTTTTTGGAGA[A/G]ACTGGTCTTGCTGTG	57674
rs562383740	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398006	GCAGTGGCTGAACAC[C/T]GGGAAGGAACTGCCA	57674
rs562387745	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329020	ATTTCTAATTCCATC[G/T]CAATCTCTGCCGAGT	57674
rs562392735	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80328235	TAGTCCTTCTCCTGG[C/T]GGCGGGGAAGGTGCG	57674
rs562404484	snp	A/G	0.000405567	0.0142344	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376982	AGTGTTGGGGTCTAG[A/G]TGACCCCACACTCCT	57674
rs562436110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296681	CTCTCAGTTTTACAC[A/G]TTTATTTATTTGTTG	57674
rs562440650	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341670	TCCAGCCCAAGAGGT[C/T]GAGGCTGTGGTGAGC	57674
rs562465708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382023	TGCACGCAAGTGTTC[A/G]GTGTGCATATATGGG	57674
rs562475819	in-del	-/GATCC			intron-variant	RNF213	GRCh38.p7	17:80282936	CTCCTGACCTCAGGT[-/GATCC]GCCCGCCTCGTTCTC	57674
rs562480323	snp	A/G	0.000101921	0.00713794	intron-variant	RNF213	GRCh38.p7	17:80332671	GGGGTTTGGAGGGGC[A/G]TCCTGCCTCAGCCTC	57674
rs562493705	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378907	AGCCAGGTGTGGTAG[G/T]TCACACCTGTAATCC	57674
rs562496338	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396623	TGATTAGCATTTATA[C/T]TGCATTCTGCATTAT	57674
rs562502278	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381815	GGGCCACCCCACACA[A/C]AGCCAGTCTGAGCTC	57674
rs562503526	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334788	ACCGCCACCACGCCC[A/G]GCTAATTTTTTGTGT	57674
rs562503776	snp	C/T	4.94189e-05	0.00497062	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376377	GCCGTTTTGCAACAT[C/T]GCTCGTGGACAATTC	57674
rs562503946	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387088	CCTGAGCCCTCTCCT[A/G]CAGGGCCATCTGCAC	57674
rs562522562	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360691	CTCCCGAGTCACAGC[A/C]CAGACACAGTGCTGA	57674
rs562534971	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300495	GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTTC	57674
rs562614707	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276212	TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCCAG	57674
rs562625657	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80280694	TCCTGGGCTCAAGCA[A/G]TTCTCCCGCCCCAGC	57674
rs562630100	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391395	CCTGCCTTAGCCTCC[C/T]TAGTAGCTGGGATTA	57674
rs562632438	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285507	GCCTGCAGTGAAGGG[C/T]TGTGCAGCACCTGCC	57674
rs562634890	snp	A/C	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80341242	CCACGCCCGGCCTGA[A/C]GTTTACTTCTTCTGC	57674
rs562655597	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390985	GAGAATTGCTTTAAC[C/G]TGGGAGGTGGAGATT	57674
rs562666773	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317077	AGCCCTGGTGTTCGC[A/G]GAGTCCCGCGCTCTC	57674
rs562667894	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80280869	GCTGTCAACGTACAC[A/G]GGTGGAAACATTCCC	57674
rs562682905	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356262	TCGCCTCAGCCTCCC[A/C/G]AAGTGCTGGGATTCC	57674
rs562683859	snp	C/T	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355818	CCGGGAATGGGGGCT[C/T]ACAGGAGAAGAAGCG	57674
rs562693792	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290019	GCACCTGTGCCAGTT[C/T]CTTGTTTCCTAATAG	57674
rs562696971	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80340418	CCGGGGCCCTTCCCC[C/G]CTCCAGCAGATGAAG	57674
rs562744965	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386618	GAGAAATGGGAGCCT[C/G]CTCCCTGCAACATAG	57674
rs562763648	snp	C/T	6.59391e-05	0.00574153	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375863	CAAGCCTCCACCCCA[C/T]GCCAGAGGTGAGTAA	57674
rs562809636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317553	TCGTTGGACTTGCGA[C/T]AGGGATGCTGTGTTT	57674
rs562810673	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305075	AGATGGAATCTTGCT[A/C]TGTTGCCCAGGTTGG	57674
rs562856972	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80333551	ATACAAAAATTAGCC[A/G]GGTGTGGTGTCAGGT	57674
rs562859954	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287325	ACATGGTGAAACCCC[A/G]TTTCTACAAAAAACA	57674
rs562892184	snp	C/T	0.00144887	0.0268763	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369559	CAGTTTCTTCGTAGA[C/T]CTGGTGTCCACCATT	57674
rs562893395	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80293862	AGGGGATTTGACCTG[A/G]AGGTCGGCAGAAGCT	57674
rs562905894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299295	TTTGGTTGGTTGTGC[A/G]GTTTCGTTTTTTCAG	57674
rs562915486	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80279672	CGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	57674
rs562944382	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355206	CATCTCTAAAAGACA[A/G]CGGACTCCTCCATGA	57674
rs562986075	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264467	GGGCCTCAGACTGGT[G/T]CCCCTCCTCCCGGGT	57674
rs563013795	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396204	GAGTTTGAGGCTGCA[A/G]TGAGCTATGATTGCA	57674
rs563044173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273915	GTGAGCCACCGCGCC[C/T]GGCCTCCACCTTCCT	57674
rs563050182	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274138	GTAGGCCTCTGCATT[A/G]AGGGTGCGTGCCCAG	57674
rs563069375	snp	C/T	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390001	CTTCATTTGCTCTTC[C/T]GTCGTTTTAGGAGCC	57674
rs563091255	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284221	AAAAAAAAATTAGCC[G/T]GGCATGATGGCAGGT	57674
rs563096079	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380754	CAGCCGTAAGCCTCA[C/T]TCCAAGTGCTGAGAA	57674
rs563133835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368289	GAGACGCCACTTACG[C/T]ACTTTCATAAATATC	57674
rs563157428	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375400	TCGTGGGCCTCTGGC[C/G]CTTAGGTAGATCTGG	57674
rs563172036	in-del	-/A	0.275197	0.248727	intron-variant	RNF213	GRCh38.p7	17:80284201	TCTGTACAAAAATAC[-/A]AAAAAAAAAAAAATT	57674
rs563180457	snp	C/T	3.29522e-05	0.00405894	intron-variant, missense	RNF213	GRCh38.p7	17:80319344	CCTGGGAAACGGATT[C/T]GGGCTCACAGCTGTG	57674
rs563209341	snp	C/T	4.95119e-05	0.00497529	synonymous-codon	RNF213	GRCh38.p7	17:80345502	CCAGGCCACCGACCC[C/T]GACAAAACGTATGAG	57674
rs563224361	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395437	TAGTGTGTTCAGACT[A/G]TGCACACAGAAAACA	57674
rs563275394	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288464	TGCCGGGGGGAGGGG[C/T]GTCCTCTGGGCCCTG	57674
rs563277788	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292676	ATGCCTCTCTCGGGG[G/T]TCCCCCACCTGGGTT	57674
rs563280765	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359759	GTTACAAGTTATCAA[A/C]GCCAGACAGGTTCAG	57674
rs563284330	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319585	TGGCACAAGTCACAC[A/G]GGCTTGCAGGCCGTT	57674
rs563313783	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80348540	ACAAATAAAGTACCA[C/T]GTCCCAGGACTGGGC	57674
rs563328364	snp	A/G	2.35863e-05	0.00343403	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374639	GTGGCATCCCTTGGA[A/G]CCTGCATGTTCCCTG	57674
rs563357555	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80296045	TTTCCCCCCAGACGG[C/G]GTCTCACTCTGTGGC	57674
rs563365641	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316876	GTGTGCTATTCTTGC[A/G]ACCTTTTTGAAAGTT	57674
rs563391103	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262740	GTCTCCCACACAGGT[C/G]AAGCCAGGGAACCCC	57674
rs563404382	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320292	GGAATCATATCATAT[C/G]TGGCCTTTTGGGTAT	57674
rs563411104	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80262982	TCTTACTGGGGAGGG[A/G]GAGAGTCAGGTCCTC	57674
rs563438759	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80268384	AAAAAAAAAAAGGCA[A/G]TACTGCATCCCCGGA	57674
rs563439224	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354712	AGCCATTCAAAGCTG[C/T]AAAGTTTTTCCCCAA	57674
rs563459576	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80337949	CAAGTTGATGCTGAT[A/G]TCTGGCAAGAAGGAT	57674
rs563479850	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303996	AAACAGTCAATATAG[G/T]CAGACCCATGGATGG	57674
rs563538857	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265665	ATCAGAATCTTCTCT[C/T]CTGTAGCCACAGGGT	57674
rs563539905	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80343484	AAGTGTGTTGTCAGG[C/T]AGTTTCCTCCTTGTG	57674
rs563545798	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358932	GAATAGGAAGTTTAC[A/G]AAGCTCTGAGAAATT	57674
rs563556826	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80325739	GAGAGACATTCCATC[C/T]TAAAAACGTTAGAGT	57674
rs563575711	snp	C/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80292817	TCCCTGCACAGTGAC[C/G]CTGAAACTCAAGGAA	57674
rs563583362	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80262315	CCTGGAGAAAAGGGA[G/T]GCAAATTGTCCCATA	57674
rs563587079	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80331306	ATGTGTCATTTACCA[C/G]TGGTTCAGCTCGTTT	57674
rs563633258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379200	TCTGTCTCATAAAAA[C/T]TGATATATGAAAAAG	57674
rs563637663	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80278500	AGCCTGGCAGGGTGC[C/T]GCCTCTGGTGTGGGC	57674
rs563648172	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324882	GAAGAAATGTAAAGT[A/G]TTTTACTATTTTGCT	57674
rs563652937	in-del	-/T	0.497147	0.037661	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356008	GACTCTCTTGATGCT[-/T]TTTTTTTTTTTGAGA	57674
rs563653365	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383393	CTATCACATATATAC[C/G]CATTAAAAATGAACT	57674
rs563667574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343602	CGCAAACCTGTGCTG[C/T]ATATGGCTGTTCTGA	57674
rs563673011	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80340996	TTTTAGTAGAGATGT[A/G]GCTTCACCGTGTTAG	57674
rs563673475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278129	GGAAGAGGAGACTGC[C/T]GGAGCCAGGGGTCAT	57674
rs563682220	snp	C/T	1.67382e-05	0.00289289	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393296	CTTACACACGTGAGC[C/T]ACCATGCTGAGGAGA	57674
rs563700411	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376127	TGCTTACGTATGTGG[A/G]TGCTGTGTTTGTATA	57674
rs563705166	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80314165	GGTGGTGGTGTAGGT[A/G]ATGGTGGAGGTGATG	57674
rs563709255	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384006	GGCCCTGGGCTTTTA[A/C/T]GTAGTATAATCATTC	57674
rs563710550	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358001	ATACATGTTTTAAAA[A/C]TAAAAAAGCAAACAC	57674
rs563711135	snp	C/G	1.7968e-05	0.00299728	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389090	TGTGGCTTGGGCAGT[C/G]AAGGGGCTCGGCTCT	57674
rs563711571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358873	GAGATGGCGCCACTG[C/T]ACTCCAGCCTGGTGA	57674
rs563775857	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324436	AAATTACACTTGATC[A/G]TGGTGTATAGTTCCT	57674
rs563823646	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330396	TGGGGTGCTGTGGCT[C/T]GACCTGGAAGTTGGC	57674
rs563830488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291961	CTCTGCATTGACCCC[A/G]CCCCAGCCTCCAGGT	57674
rs563833520	in-del	-/ATCT	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80268601	CATCCTCTCTCATCC[-/ATCT]GTTTGTCCATCCATC	57674
rs563860434	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80336978	GTCTGAATTGACGTA[C/T]GCAGCTTAACTAGAT	57674
rs563876998	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282467	GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT	57674
rs563890194	in-del	-/GAGT	0.398308	0.201258	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364399	TCCTTGGTGGGAGCC[-/GAGT]GAGTGAGTGAGTGGC	57674
rs563890623	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367683	GTGGTGCTCCCTCTG[C/T]CGCCCGGCCTGGCCG	57674
rs563904601	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388124	GCCCGCCACCATGCC[C/T]GGCTAATTTTTTTGT	57674
rs563919719	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80296930	GTGATCCGCCTGCCT[C/T]GACCTCCCAAAGTGC	57674
rs563932451	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312446	CCTCCGGGTCAGGAG[C/G]CTGGCTGTGGTCTGG	57674
rs563969682	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311924	CAGAGGTTAGGAGTT[C/T]GAGACCAGCCTGGCC	57674
rs563978088	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387680	TGGACCTGCCTGGCC[G/T]CTCATGGCATATGGG	57674
rs563994248	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80307357	GGTTATTAATATTGT[C/T]GTCTGTTTTTTTTTT	57674
rs563995982	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393675	TTTTTGAAAGCCGAG[C/T]TGTTTCTGAACCATG	57674
rs564044315	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260140	ATCAGTGACAGAGCG[C/T]TCCGCGCGGGGCCGC	57674
rs564060161	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372868	TCCCCTGGATGTGTT[G/T]CTGTGAATGCCTGTG	57674
rs564073816	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80330075	TTATTCAGAACCAAA[C/T]TTTCTGCTTAGGTTT	57674
rs564100616	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80290633	CTCTCTTCATTTCCC[A/G]TTCAATCCTGACCTC	57674
rs564115239	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80348580	TAGGGACGCACAGAT[-/G]AATCTGTAGCCCTTG	57674
rs564134338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378267	GGCTGCATTATTAGC[C/T]CTCAGAGGAGGTGTG	57674
rs564159596	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80290431	TGTGTGCGAGTGTGC[A/G]CGTGTGTGCATGTGT	57674
rs564162001	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296042	TGTTTTCCCCCCAGA[C/T]GGCGTCTCACTCTGT	57674
rs564191274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377875	GATCGTGGGTCAGGA[A/G]AGTGAGGCTCTCGGC	57674
rs564226426	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80267714	TCATCTCCATAACAT[A/G]AAAGTGCAAGGTGAA	57674
rs564237587	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352594	AGAATGGAAGGCAGA[C/G]CTTGCCAGTGTCCCC	57674
rs564259370	snp	C/T	9.89332e-05	0.00703255	synonymous-codon	RNF213	GRCh38.p7	17:80347489	AAAAACTACGTGGCA[C/T]TGCAGATCCTGCAGC	57674
rs564270609	in-del	-/AAGGTAGGAGGATTGCTTGAGCCTGGGGAGGTC	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379093	GCTACTTGGGAGGCT[lengthTooLong]AAGGCTGTAGTGAGC	57674
rs564276237	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352011	AGGCGTGCGCCACCA[C/T]GCCCAGCTAATTTTT	57674
rs564277138	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80281908	TTTGCCCAGGCTGGA[A/G]TGCAATGGCGTGATC	57674
rs564334514	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80318644	AGTGGCGGGATCTCG[A/G]CTCACTGCAAACTCC	57674
rs564335278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365843	GTCCAGCGTGGGTCA[C/T]AAGGGCCAGGTGCCC	57674
rs564355620	in-del	-/GTGGC	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80334682	CCAGGCTGGAGTGCA[-/GTGGC]GTGGCGTGATCTTGG	57674
rs564368010	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271919	CAGGAGGTGGAGGTT[G/T]CAGTGAGCCGAGATT	57674
rs564370564	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270828	CTTGAGGGGTTCAAG[C/T]GTACTAGGGCTTTGC	57674
rs564371382	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383273	CTCCTACAGCTGGTC[A/G]TGAAGTCAGTCCGAG	57674
rs564391222	snp	A/G	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80318343	CGAAGGTGGGGTTTT[A/G]CCAGGGACCCGCCCC	57674
rs564394420	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371617	ACATAAAAGCTCTTC[A/G]GGGTTCTCAATTTTT	57674
rs564400182	in-del	-/AAAT	0.00404039	0.0447646	intron-variant	RNF213	GRCh38.p7	17:80304643	GACTCCAACACAAAT[-/AAAT]AAATAAATAAATAAA	57674
rs564426967	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322563	CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA	57674
rs564449403	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370184	CTGGTTCCACAGCAG[C/T]GCAACTTTCTGATTT	57674
rs564472104	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286400	CAGGAAGTGTGGCCA[C/T]GTGTGATAGAGAAGG	57674
rs564473066	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80295310	CTGCGGTGCAGCCTG[G/T]GTGGGTTTCAGGCCG	57674
rs564475716	in-del	-/TT	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80318998	TGGGAAAAGAGACTC[-/TT]TTAAATTTTAGCCTT	57674
rs564484191	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341121	TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTTCA	57674
rs564503771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350681	CAGTGCACCTCTAGT[C/T]CCAGCTGCTCAGAAG	57674
rs564513706	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80328900	CACGAAAGAAACCGT[C/T]ATCATTTTACAATTT	57674
rs564521343	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80300392	GGGATTGGTAGTGTG[C/T]GCCACCACATGTGGC	57674
rs564531942	snp	C/T	4.95193e-05	0.00497566	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367754	TTTCTTCAGTGTCTT[C/T]GAGAGAACTCTGACG	57674
rs564537703	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259340	AGGCTTGGTGGCGGG[C/T]GCTTGTAATCCCAGC	57674
rs564539096	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355685	ACAGGGGGAAGAAGC[G/T]GGGTGACCGGGAATG	57674
rs564565973	in-del	-/TA	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80299213	CAGCAAATTCTTGTC[-/TA]TGTCTTAGCGTTCCA	57674
rs564570727	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80323051	CCATTTTGAGTTCCT[C/T]TTTATATATGGTGTA	57674
rs564591102	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287084	TTCAAAACCAGGCCA[C/G]GCACGGTGGCTCACG	57674
rs564591223	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397797	TTTCTTGGTTCCCTG[A/G]CCAGGAATCTAGGTG	57674
rs564628562	in-del	-/CT	0.00914312	0.0669923	intron-variant	RNF213	GRCh38.p7	17:80272910	GGAAAGCGTAACAGG[-/CT]CTGTTTTAGAGGTGC	57674
rs564633116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270468	GGCCACTCACTGGCC[A/G]CGTCTCTGTGCTCCC	57674
rs564689090	in-del	-/GGG	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80274900	GGATGTGTGTGTGTT[-/GGG]GGTGTGTGAGTGGGG	57674
rs564696129	snp	G/T	3.87642e-05	0.00440234	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376852	ACAAGCTCACTTATC[G/T]AGAGCTGTCTCTGTC	57674
rs564711075	snp	C/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287640	ACCCTGCCCACCCCC[C/G]ACTTTTGTTTCTTAA	57674
rs564757182	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365431	GGAGTCAGGTGCCCA[C/T]GCTCCGTCTTGTCCC	57674
rs564792915	snp	A/C/G	3.93811e-05	0.00443726	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381740	GAAGTGAGGAAAGGG[A/C/G]CAAGGGCTGGGCGGG	57674
rs564795932	snp	C/T	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80266021	GAGTTCCAAATGATA[C/T]AAAGTTGAGTCAGGT	57674
rs564798995	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359017	CAGACCCAGCATGGC[A/G]TGACACGGAGACAGT	57674
rs564816184	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341590	CTGTACTTTAAAAAT[C/T]AGCCAGGCATGGTGG	57674
rs564829167	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391331	GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTTAG	57674
rs564832198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386549	CACTCCTTCAGCCGC[C/T]CCCACCAGTGACCCG	57674
rs564835717	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300848	TGAGCCACCATGCCC[A/G]GCCTCATTGTGATTT	57674
rs564866809	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310838	ATTACAGGCATGAGC[A/T]ACTGCACCCGGCTGA	57674
rs564901999	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317535	GGATTTTTCCTGACC[A/C]CTTCGTTGGACTTGC	57674
rs564918581	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80275883	TGGCCAGGATGGTCT[C/G]GATCTCCTGACCTTG	57674
rs564933704	snp	A/C/T	4.96153e-05	0.00498052	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386301	ACTTGGATCTGGACA[A/C/T]TGAGTTTGAGATCCT	57674
rs564964914	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305680	GCAGTGGCGTGATCT[C/T]GGCTCACTGCAATCT	57674
rs564999544	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280589	CTCCCGAGTAGCTGG[G/T]ACTACAGGCGTGCAC	57674
rs565004625	snp	A/C	0.000114554	0.00756729	missense	RNF213	GRCh38.p7	17:80337703	GGCATCTATGTGATC[A/C]AGGCGCCCAAAGGTG	57674
rs565027940	snp	C/T	0.00029656	0.0121734	missense	RNF213	GRCh38.p7	17:80346109	GACGTTGCTGAAAAG[C/T]TCTACATCCAGCAGA	57674
rs565084167	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	RNF213	GRCh38.p7	17:80345337	TGTCGATGCCATCAG[C/T]CACTTGACTGGGAAG	57674
rs565101547	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293816	TGGGCGACAGAGGGA[G/T]ACTCAGTCTAAAAAA	57674
rs565102144	snp	A/C/G	0.00126845	0.0251533	stop-gained, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364441	TTGACAGAGCCCAGT[A/C/G]GAGTCGGATTTTCTC	57674
rs565105601	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80282099	TGACCTCAAGGAATC[C/T]GCCTGCCTTGACCTC	57674
rs565126494	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395610	CCCCATGCCCTGCCT[A/G]AAATGACTTCACTGG	57674
rs565127898	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80316827	TGTGAAGCGTGAATC[C/G]CACAGGACTGGAGTT	57674
rs565129608	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326845	GTTTTTGCAATGATT[A/G]GTAAAGCTACTATGT	57674
rs565145900	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80293599	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	57674
rs565161982	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396164	CTACCTGGGAGGCTG[A/C]GGTATGAGGATTGCT	57674
rs565163576	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380733	CTCTTCACATAACTC[C/T]CTTCTCAGCCGTAAG	57674
rs565166875	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316234	TCCAACCCAGGTGAC[A/G]GAGCGAGACCCTGTC	57674
rs565191129	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309858	CCTCCTGGGTTCACG[C/G]CATTCTCCTGTCTCA	57674
rs565192299	snp	G/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287594	CGTGACCGTGCCGAG[G/T]GTGGCGAGCGCTTCA	57674
rs565201623	snp	A/C	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390922	CAAAAATTAGCCAGG[A/C]ATGGTGGTACACACC	57674
rs565226038	in-del	-/CTAA	0.0103295	0.0711199	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384430	TGGAAATATACTTTC[-/CTAA]CTTTCACCCATTTGC	57674
rs565227308	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289998	TTAGGAGGTGGAGGG[C/G]GGTGGGCACCTGTGC	57674
rs565228391	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80284924	GGGTCCCTATGGCCA[A/G]GATGATAGACATCAG	57674
rs565230620	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263542	CCATTAACCAGGGGA[C/G]CAGCTGGGCTGCTGT	57674
rs565239146	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80269806	TACCTGTCTACCTAC[C/T]TACCTACATATTCTA	57674
rs565239562	snp	A/G/T			intron-variant	RNF213	GRCh38.p7	17:80323885	GAATTCTGTTTCCAG[A/G/T]TTGTTCCTTGCTGGT	57674
rs565250935	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80269481	ATTCATCTATTCTAT[C/T]TATCCATCCATCCAT	57674
rs565272742	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375280	CTCGCCAGAAGACTG[A/C]CCATGTGGGGCATGA	57674
rs565279587	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80298794	ACATGGTGAAAACCC[A/G]TCTGTACGAAAAATA	57674
rs565290003	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80284173	ACCAGCCTGGCCAAC[A/T]TGGTGAAACCCCATC	57674
rs565291256	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213	GRCh38.p7	17:80304557	AGGCAGGAGAATGGC[A/G]TGAGCCTGGTAGGCA	57674
rs565308438	in-del	-/TT	0.49423	0.0534032	intron-variant	RNF213	GRCh38.p7	17:80307855	ATGCCTGGCCGTCTG[-/TT]TTTTTTTTTTTTTTT	57674
rs565310188	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374763	ACCTGGCTAGTGTGC[A/G]TGAACCAGTGGCTGG	57674
rs565338038	in-del	-/TTC			intron-variant	RNF213	GRCh38.p7	17:80310203	TTTCACCCACTTGAG[-/TTC]ATGAGTTTCAGTTTG	57674
rs565353320	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80288983	CACCCAGGTGGGCCC[C/G]GAGGTACCATGGCAC	57674
rs565403500	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80315299	GGTGGTGGTGGTGGA[A/G]GTAATGGAGGTGATG	57674
rs565406582	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385456	GGAAAGATGGGCTCT[C/T]GGCAGAGCATGTAAC	57674
rs565433718	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379505	AGCACACACTGGGAC[A/G]ATCTGAGGGTGCTCA	57674
rs565449529	snp	C/T	0.000228885	0.0106953	intron-variant	RNF213	GRCh38.p7	17:80278750	CCTGTCTGAAGGGGG[C/T]CGTGTTTCAACAGGG	57674
rs565478941	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354051	CACCAGGCTGCTGAG[A/G]AGCTGTGTGCAGAGC	57674
rs565491151	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388518	GCAGCGCGGCACTAC[A/G]CTGCAGTTTTCCGGC	57674
rs565491233	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359092	CTGTGCTCCCTCCCC[A/G]TCCCTCATTCCCTGG	57674
rs565539270	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291503	GTTGGGATTTCAGGC[A/G]TGGGCCACTGAACCC	57674
rs565547916	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297053	TGGAGGCAAAGGCAA[C/T]GTACAGAGTTAGTGC	57674
rs565561520	snp	A/G	3.295e-05	0.00405881	missense	RNF213	GRCh38.p7	17:80344859	ATTTAAGACGATTCA[A/G]TCAAAACCAAGACCT	57674
rs565577597	snp	A/C	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385103	AAAGGGATCTAGTGA[A/C]GCAGTTCCAGAACGT	57674
rs565598066	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349648	GTTTGGATTCTGTGC[C/G]GTTGTGTGGCAACTG	57674
rs565605601	snp	A/C	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80308272	CTTGAGGATCCCCCC[A/C]ACAAGCTCCCTATCT	57674
rs565655016	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358548	ACCCTAATATGCTCT[C/T]CCAAGTGCTGGGTGA	57674
rs565686171	snp	C/G	1.65021e-05	0.00287241	missense	RNF213	GRCh38.p7	17:80348248	CTTCAGGCACACCTG[C/G]ACACGGCAGACCTGG	57674
rs565690105	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80330020	CATCATTTTTCTCTC[A/G]GATTTTCTATCTCTG	57674
rs565693373	snp	A/G	0.000386264	0.0138918	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287856	AAAGAAGGGGAACAA[A/G]TCCGCTTCCTCAGAG	57674
rs565704587	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80267874	TCCCAGGCTGGAGTG[C/T]AGTGGCTGGTCCTCA	57674
rs565725085	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362278	CCTAAAAATTTTAAA[C/T]TTCAGTACATAAAAA	57674
rs565728840	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259441	CACTGCACTCCAGCC[C/T]GGGGTATAGAGTGAG	57674
rs565744147	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384120	TATGATTGCCAGAAG[C/T]GTAAAGTCACAGACG	57674
rs565753556	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276781	TCCTAGGCCGGGCGC[A/G]GTGGCTCACACCTGT	57674
rs565764790	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80278233	TGCTGTGAGGTCTCC[C/T]GGCGATGCCCGGTGT	57674
rs565778768	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377525	ATGGGCCTATATTCT[A/C]ATTGCTCTTTACTTG	57674
rs565819832	snp	C/T	1.64762e-05	0.00287016	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353675	CAGTGATGTAAGTTC[C/T]GGTTCTTGGGACCTC	57674
rs565827982	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80277777	GAGAGCAGTGTATGC[A/G]TGAACGGTGCTCTAA	57674
rs565841776	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378003	CTCAGCACTGTGGAC[A/G]TGGCTCTGCGGCGTG	57674
rs565849994	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260302	GGGCGCCGGGGCGGG[A/G]GGCGCGCCTGTCCCG	57674
rs565852800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323925	CACAGTGCTCCATGC[A/G]TCTTGTATCCTGCAA	57674
rs565855968	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367477	ATTATTACTTAAAGT[A/C/T]TGAAATATCTTAGTG	57674
rs565871980	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287485	CCATCCTGGGCGACA[C/G]AGGGAGACCTTGTCT	57674
rs565878779	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338740	TATCACTTGAGGTCA[A/G]GTGTTTGAGACCAGC	57674
rs565885374	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80323462	AGGGCTGGTATTCAA[C/T]GTATAGATCAGTTTG	57674
rs565891133	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271619	CCCAGGATTGAAAAC[A/C]GGGACTCCTTGAAGG	57674
rs565892663	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80280903	GAGTAACAGAGGCGC[A/G]ACCTGGGGATGCGCA	57674
rs565940303	snp	A/C/G/T	0.0001345	0.0081996	synonymous-codon	RNF213	GRCh38.p7	17:80347161	AGCCTACGAAACGGT[A/C/G/T]TGTAAGCGCCAGGAC	57674
rs566007021	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80348673	ATGATAAATGCTGTG[C/T]TTAGAGGCAGCGGGG	57674
rs566027645	snp	C/T	0.00126879	0.0251553	synonymous-codon	RNF213	GRCh38.p7	17:80347800	CATTGAAGAGAAAGA[C/T]GTCGTGTACAAACAC	57674
rs566063082	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80303621	CAGGCTGGAGTACAG[C/T]GGCGCGATCTCTGGT	57674
rs566073253	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320543	AAAGAACAATGTGCC[A/G]CCACACTCGGTTCCT	57674
rs566078100	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80281421	CCCAAGACAAACACC[C/T]CATTCACACCACTCA	57674
rs566105857	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80312637	TGGCTGTCTCCTGTG[C/T]CTAAGGAACAGGCCC	57674
rs566121428	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80323967	TCATTTGGTAGCTCA[A/G]ATTGTGTGTGCGTGT	57674
rs566132601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305747	CTCCTGAGTAGCTGG[A/G]ATTACAGGATTACAG	57674
rs566136627	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80330368	TGGGTTGGCCCTCTG[C/T]GGGGTGCTGCCGTGG	57674
rs566169065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336687	GTAATTGTCATTTTA[C/T]TCTGTTACTTTTTGT	57674
rs566175833	in-del	-/TGT	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80309790	GACGGGGTCTCACTC[-/TGT]TGTCACCCAGGCTGG	57674
rs566182056	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361069	GTTCCTAATTTACTT[G/T]GACCCGGGGGTTCCT	57674
rs566203871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342440	TTGAATCTGATGTTA[C/T]GTTGCATCAGTTTTG	57674
rs566223812	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80286614	TTACCAGTTGCTGAG[G/T]AGAGGGTGGATTAGC	57674
rs566224990	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259477	CTCCAAAAAACAAAC[A/G]AACAATAAATAAAGT	57674
rs566238990	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259147	TGGAGACCCAGCAAA[C/G]CGAGAAGATGCCCAA	57674
rs566247892	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80329378	TTTCAATGTGCTGCG[C/T]CATCATTGCCTCCAC	57674
rs566270223	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328654	ATTCTTCTTTTTGGT[A/G]TTTATGTCCACATTT	57674
rs566271892	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296240	GGCCAGGCTGGTTTC[A/G]AACTCCTGACCTCAA	57674
rs566285591	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290786	CATAGGATGCCCAGC[C/T]TGTGACACGTAGTTT	57674
rs566294227	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352096	TTGACCTCATGATCC[A/G]CTCGCCCCAGCCTCC	57674
rs566320605	snp	A/C			utr-variant-5-prime	RNF213	GRCh38.p7	17:80263679	GCAGTCCCAGCAGGA[A/C]CCATGGAGTGTCCTT	57674
rs566323929	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392374	AATAGAATACAAGGT[G/T]TTTTGAATGGTGAGG	57674
rs566330389	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294024	GAGGCCTGTCCGGGC[G/T]CTTCCCATTTCTGCC	57674
rs566342128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312085	GTGAGCCAAGATCGC[A/G]CCACTGTACTCCAGC	57674
rs566350214	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80315102	AGGTAATGGAGGTGA[-/TGG]TGGTGGTAAAGGTGA	57674
rs566381138	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318437	AGGCCTGCCCATAGG[C/G]AGGAAGTCTAAGTGG	57674
rs566385203	in-del	-/G	0.0185938	0.0946107	intron-variant	RNF213	GRCh38.p7	17:80301459	TCAAACAAGTGAACA[-/G]AAAAACTCAGATCTA	57674
rs566417101	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334731	TCCCGGGTTCACGCC[A/G]TTCTCTTGCCTCAGC	57674
rs566419054	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341296	GGGGTTGATGTTGGT[C/T]GTGTGAGCAAGGGGA	57674
rs566425716	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322351	AAAATTTCTGTGGGC[C/T]GGGCATGGTGGCTCA	57674
rs566457787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340687	GTACAGTGGCGTGAT[C/T]TTAGCTCACTGCAAC	57674
rs566479679	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290474	ATGTGTGTGTGCACG[C/T]GTGTGTGCGCACGTG	57674
rs566492457	in-del	-/AT	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380161	ATGAAGGAGACAGAC[-/AT]AGTCTTATGAAATAC	57674
rs566511895	snp	C/T	3.29457e-05	0.00405854	missense	RNF213	GRCh38.p7	17:80346190	GTGATCACAGAAGTC[C/T]TCTGCGCCTCTCAGG	57674
rs566514850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365981	AACTTACTGGGTTTC[C/T]GGTTTATTTCCTTCC	57674
rs566546584	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396893	ACTGGAGGGGCCCTG[A/G]GTCCAGCAAGTGCTC	57674
rs566559874	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80350820	AAAAAAGGTGAAATG[C/T]GAGAGGTGTAAATAA	57674
rs566565684	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320776	GCCCAGGAGTTCAAG[A/G]CAAGCCTGGGTAACA	57674
rs566573149	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396257	ACAGAGTGAGACCCT[A/G]TCTCAAAAAAAAATA	57674
rs566577709	snp	C/G	0.0596104	0.162024	intron-variant	RNF213	GRCh38.p7	17:80311022	TCTCTGGAGTGGCTG[C/G]TATTTAAACCGCCAC	57674
rs566591778	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80317580	GTTTACTTGGCCCGC[C/T]GTGCTCAACCCCTTG	57674
rs566626160	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321599	CGAGTCCCACAGCAG[C/T]TGAACCATTTTCAAT	57674
rs566626822	snp	C/G	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80274822	GGGTGAGGGGGGTGT[C/G]TGTGGGGGGTGAGTG	57674
rs566628188	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80317345	CCCCAGACCATTAGC[A/G]ACAGCCAAGAGATCT	57674
rs566640463	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80275375	GGATGGTGTTCCTTG[A/C]AAACATTGAAGGCAA	57674
rs566649183	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80336139	ATAGTCCCACGCTGA[A/T]CTCCCCTCTTCTCTT	57674
rs566662259	in-del	-/AG	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374147	TACCACCTGGGGTTT[-/AG]AGTTGACATGACTTG	57674
rs566689614	in-del	-/T	0.00835141	0.0640778	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366668	AAGGATGGCTCAAAA[-/T]AAAAAAAAAAAAATC	57674
rs566695988	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270664	GTGTATTTCCTTGAG[A/C]GGCCTGTCTGTCTTT	57674
rs566710985	snp	A/G	0.000131785	0.00811635	missense	RNF213	GRCh38.p7	17:80306389	TTGAGCACCTGGGTC[A/G]TTTTCCTGCTCATAT	57674
rs566713769	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381380	GAAAAGCCAGCAGCC[A/G]TTCCGCTTGCTAGCC	57674
rs566722208	in-del	-/GT	0.00239473	0.03452	intron-variant	RNF213	GRCh38.p7	17:80290369	TGTATGTGTGCGTGT[-/GT]GAGTGCGTGCACGTG	57674
rs566727319	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370683	CACTCCCACTACACA[C/T]CGGAGTAGACAGTTG	57674
rs566738002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270938	TCCCAGCACCACCTC[A/G]TGGTCTTTCCAGGAT	57674
rs566738497	snp	A/G	0.000197658	0.00993931	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376411	GCCATTGTTGAGGGC[A/G]GGGCCTAGTGACAGC	57674
rs566740787	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80263223	CCTGGGCTGCCTGCT[C/T]AGGCCCCATCACCTG	57674
rs566748271	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300180	CAGTGCATAAGCATT[C/G]CTTTTTCTCCGCAAC	57674
rs566756383	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375467	AGCACTTTGGGAGGC[C/T]GAGGCATGCAGATCA	57674
rs566776978	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376122	ATTAATGCTTACGTA[C/T]GTGGATGCTGTGTTT	57674
rs566777391	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381857	TTGCTGGAAAGAATG[A/G]GAGAACACACAGAGA	57674
rs566785729	snp	A/C/T	0.000148894	0.008627	missense	RNF213	GRCh38.p7	17:80346470	TCGCCAGGTTCTTTC[A/C/T]GAAACCGTATGACGA	57674
rs566835356	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391017	CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA	57674
rs566856791	snp	C/T	0	0	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360475	TAGTGCCGTGATGGC[C/T]AGGGATATGGCGAAA	57674
rs566858644	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355384	GGAGCTTACAGGGGA[A/G]GAAGCGGGGTGAATG	57674
rs566863029	snp	A/G	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80285015	TCAAACCATGCAGCC[A/G]ATAACAGGGAGAGCC	57674
rs566911303	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80304355	AATAATAATTAAGAG[G/T]CTTGGCTGGGTGCAG	57674
rs566920908	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80310530	AGTGCTGGGATTGCC[A/G]ATGTGAGCCACTGCA	57674
rs566940031	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80300199	TTTCTCCGCAACCTC[A/G]CCAGCATCTGTTATT	57674
rs566946151	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392093	CTTCTTGTGCTTTCA[C/T]ATACTTGTTTTATTC	57674
rs566949148	snp	C/T	8.23811e-05	0.00641746	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369634	CCTGCTCTCTCTCCT[C/T]TTCGTCCAAAAGGGG	57674
rs566964339	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379965	TAATATGAATACAGG[C/T]GTCTTCCTTTTGGGC	57674
rs566965878	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80350740	GGAGGTCAAGGCTGC[A/G]GTGAACTGCGATCCC	57674
rs566973289	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385815	CAACCTCTGCCTCCC[A/G]GATTCAAGCAATTCT	57674
rs566984503	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80285566	TCTCAGCAGGTCCCC[C/T]GGCAGCTGACCAGCC	57674
rs566992868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350443	GTAAAAAACCCAAAA[C/T]GTAGGAAGTCCTAGA	57674
rs566997669	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304611	CACCACTGCACTCCA[C/G]CCAAGGCAACAGAGT	57674
rs567005143	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333150	GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGTCTC	57674
rs567026604	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380524	GCCCAACCGCTCCTC[C/T]CCTGACAAAGACTTC	57674
rs567029078	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327091	AAGTGTCTCCCTAAG[A/C]CCATCCTGATAGACA	57674
rs567052227	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293595	TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	57674
rs567068707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364214	GGTACCCCATGCAGA[A/G]GCATCACAGTGGGAC	57674
rs567071221	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80333648	GCAGTGAACCGAGAT[C/T]GTGCCACTGCACTCC	57674
rs567080113	in-del	-/TTTTTT			intron-variant	RNF213	GRCh38.p7	17:80273631	TTTTTTTTTTTTTTT[-/TTTTTT]GAGACAGAGTTTCGC	57674
rs567080962	snp	G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394485	CCGAGCCCGGATCTT[G/T]TGCTGCTTTTCTCAC	57674
rs567091092	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376725	CTTGCCCTTTGTTAT[C/T]TCACAGGAAGCTGTT	57674
rs567116119	snp	A/G	0.000247131	0.0111133	intron-variant	RNF213	GRCh38.p7	17:80349744	CTTGAAGTCTGGCAA[A/G]TAATTTGCATTTCTT	57674
rs567116284	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80283331	CTCCGAGGTGTCAGC[C/G/T]CTGCAGGTGTGATGA	57674
rs567139348	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371202	AAAAATGCACTGATA[C/T]AGTTTCAGGCTCCAC	57674
rs567149131	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358676	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	57674
rs567160399	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354754	TAGGTCTGGACAGTG[A/G]CCAAATGGCAGGTGC	57674
rs567166114	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326492	TAAAGTCCATAGTTC[A/G]TTCCTGGTGTTGTCC	57674
rs567204044	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384789	CAGCCTTTGATGGAC[A/G]CGGCTGATGCGTCAG	57674
rs567206979	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273530	GAACCTGCCCACAGG[A/G]CAGCAGCAGAGCTGC	57674
rs567228048	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269595	TATCTATCCGTCCAT[A/C]CTATCTGTTTATCTA	57674
rs567235127	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80344549	AAAAAGACTATACAG[A/G]AAGCTACATATTTTC	57674
rs567255994	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349421	ACGAACTCCATCTGA[A/C]AGCATGAGTCGTACT	57674
rs567280366	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309540	GTTTGCAGAGAACTA[C/T]GGGGACCATTTTCCT	57674
rs567291293	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274000	GGGGCCTGAGCTTCT[A/G]CCGTGTGTATCTGTG	57674
rs567296495	snp	G/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80316942	CTTTCAGAATAAAAA[G/T]CCGGTTGTGCAGTAG	57674
rs567334975	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375361	GGCTGAGGCATGTGA[A/G]AAGTTTCTTTTCACA	57674
rs567345378	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352385	ATGTAGGTCACACGG[C/T]GTGGAGACTCCCGAC	57674
rs567359007	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80339160	GCGTGTTACCCTCTC[A/G]CATGGCTCTGTGAGC	57674
rs567382194	snp	A/G	0.000120344	0.00775613	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363562	GGCCTCTGGTGGGCC[A/G]GTGGGAGGGGCACCG	57674
rs567383407	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307412	TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGACGCA	57674
rs567384020	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384110	TATCAAACTGTATGA[C/T]TGCCAGAAGCGTAAA	57674
rs567395578	snp	A/G	0.02016	0.0983543	intron-variant	RNF213	GRCh38.p7	17:80269397	TCCACCTATCCATCT[A/G]TCCTATCATCTATCC	57674
rs567396131	snp	A/G/T	3.29464e-05	0.00405861	missense	RNF213	GRCh38.p7	17:80345048	TCTTCTGCAATCCGA[A/G/T]TTTTATTGGCGACAC	57674
rs567431309	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261815	CCTGAGGTCGGGAGT[G/T]CGAGACCAGCCTGGC	57674
rs567456719	snp	C/T	6.88919e-05	0.00586866	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288333	AGAACTGCAGACCAC[C/T]GAGCAACAGGCAGGG	57674
rs567469482	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377265	GAACCACATCAGAGA[C/T]GCATTCAAAGGCCCA	57674
rs567482268	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383948	GTCTGGCTTACTGTG[A/G]CTCCCTCCCTCTTTC	57674
rs567482276	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361486	GATCACGCTACCCAC[C/T]GCACTCCAGCCTGGG	57674
rs567569231	snp	A/G/T	0.00517822	0.0506191	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389427	GGTCTCCTGCTTCCC[A/G/T]CGAGGGATAGGAGCA	57674
rs567569766	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320101	GTAGTCACAGATATG[A/T]ACAGTCATCACCACA	57674
rs567596807	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80268015	ATTAGAGATAGGGTT[C/T]CTCCATATTAGCATT	57674
rs567611527	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343643	CAATTGTAAAACGGT[C/G]TATTTATGTGTCTAA	57674
rs567615694	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368428	CAAGGAATGTAGACG[C/T]CAGTGTTTTTTTTTT	57674
rs567634067	snp	G/T	0.000231562	0.0107577	missense	RNF213	GRCh38.p7	17:80332262	CGCAGAGTTGCTGAG[G/T]GAGCCCGAAGAAGAA	57674
rs567639294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298130	CGGTGAGGGCCTGCA[A/G]AGGAGCTGACGCCCT	57674
rs567647577	snp	A/G	0.000100241	0.00707886	missense	RNF213	GRCh38.p7	17:80343254	AGCCGAGTCCTGGGC[A/G]CCCTGCTGCCCTTCC	57674
rs567658257	snp	C/T	1.6552e-05	0.00287676	missense	RNF213	GRCh38.p7	17:80348003	TCATCGGCTACCACT[C/T]GGACGCCTGCGCGTC	57674
rs567662792	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394127	AGAGGGTAAGAGCCA[A/G]AAGCCTCATTGTGAA	57674
rs567665250	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356024	TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT	57674
rs567738502	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80325254	GTGGTGTCTTCCTGA[C/T]TGGGAAAGGTGGGAG	57674
rs567757871	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80323837	AGTACTTTTTTTTGG[G/T]GGGGGGTGCTATTGT	57674
rs567759967	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398921	CTGTAACACTCCAAT[A/G]CCACTTTGTTGTCAG	57674
rs567765494	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80331685	GGCATGAGCCACTGC[A/G]CCCAACTAGTTTATG	57674
rs567827077	snp	G/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80263518	TTGGGCTGTGCTCCT[G/T]TTGGGTTTCCATTAA	57674
rs567840884	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357373	TCCATCCCTCCGCCT[A/G]CCTGTCCATCCACCC	57674
rs567857036	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353233	ATAGAGCACCAGGGC[C/T]GAGCAGGTGCGCTTA	57674
rs567860085	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314955	GAGGTACTGGAGGTG[A/G]TGGTGGTCGTGTAGG	57674
rs567864193	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80261787	ACTTTGGGAGGCCAA[A/G]GCGGGTGGGTCACCT	57674
rs567870528	snp	C/T	0.00795532	0.062565	intron-variant	RNF213	GRCh38.p7	17:80267905	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	57674
rs567871762	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80282508	GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC	57674
rs567897744	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80313271	AGGGGCAGTTGTTGG[C/G]CTTCACCTGAGCCTC	57674
rs567923931	in-del	-/AG	0.00478085	0.0486577	intron-variant	RNF213	GRCh38.p7	17:80333388	CTTATGTTTTTAGGT[-/AG]ACCGAGATAATGATT	57674
rs567940222	in-del	-/G	0.0123036	0.0774623	intron-variant	RNF213	GRCh38.p7	17:80284212	ATACAAAAAAAAAAA[-/G]AATTAGCCGGGCATG	57674
rs567967083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384076	TAGCAGAAGACTCAG[A/G]GCTAGAGATCTTCAT	57674
rs567969061	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378725	CCATGAAATGAGGAC[A/G]CTGAAATAGAGTCTA	57674
rs568008577	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393029	GTGGCCCAGGCTGGA[C/G]TGCAGTTGTGCAATC	57674
rs568021618	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398326	TGTTTTGTCTTGAAG[A/C]AGCATGGGTCAAGCA	57674
rs568045709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362754	TTTTCAGCTTTGCTT[C/T]GAAAAATAAGAAATA	57674
rs568065499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80281318	CACACATACCCCACT[C/T]ACACCACTCACACAC	57674
rs568104482	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80262621	TGGATTTCCTTTATA[G/T]CCTTTTACAAAAGGA	57674
rs568109884	snp	C/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352765	ATCGGGTCGTGTATA[C/G]TATCGGGTTGGGTGG	57674
rs568116006	snp	A/C	0.00557542	0.0525036	intron-variant	RNF213	GRCh38.p7	17:80335958	CTCCAGCTTGGGTGA[A/C]AGAGTGAGACTCTGT	57674
rs568116705	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296609	GTGTGTTGATTTGAA[C/T]GTGAGAATGACATTA	57674
rs568139810	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80296309	GTAGGCGTGAGCCAC[A/C]GTGCTGGGTCTGAAT	57674
rs568160763	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381921	CTGGAAAAAGGAAGC[A/G]CTCTGCTTGCCCAGA	57674
rs568162780	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387340	CGAACTCTTGGGATC[A/C/G]AGGGATCCACCCGCC	57674
rs568188989	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307005	AGCACCTTAAAATTT[C/G]TTTGTAGGAAGAAAA	57674
rs568192436	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282243	GAACAGTTGCTACAC[C/G]GTGCGGTGTTGCTCT	57674
rs568192575	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287759	AGTTGGAGGGAAACA[C/T]GGGCTAGAGTAGAGT	57674
rs568194044	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358083	TTCCATTCCAGTTCC[A/G]TCTCTAATCTTAGAC	57674
rs568216602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80342394	GTGAGTAGGTAACGG[C/T]TGGGAAATGTGAAGG	57674
rs568220085	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366087	CCCCTACCCAGCCCC[C/T]GCTGAAGAGCAGCCC	57674
rs568226564	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80290912	CCTCCTGGGTTCAAG[C/T]GATTCTCATGCCTCA	57674
rs568227110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306623	TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT	57674
rs568238713	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80323893	TTTCCAGATTGTTCC[C/T]TGCTGGTGTCTAGAC	57674
rs568240235	snp	A/G	3.35638e-05	0.00409643	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372621	ATTCTCCAGCAAGCC[A/G]GGGCCGAGAGCCTGC	57674
rs568315970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275959	GAGCCACCATGCCTG[A/G]CCAGTTTTTTTTTTT	57674
rs568322320	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80290304	GTGTGTGTGCATGTG[G/T]GTGTGTGCGTGTGCG	57674
rs568327969	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272571	GGCACCAAGCCATTC[A/G]TGAGGGATTTGCCCT	57674
rs568336473	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360556	TCCCATTCTGGGCCT[C/T]CTCAGACTGGGGCAC	57674
rs568359892	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80336638	CAGAAGGGAAATATG[C/T]TGAAACGTTGCCAGG	57674
rs568361498	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379842	TGGGCCTGTGTCATA[C/T]TGAATAGCAATGCCA	57674
rs568370548	snp	A/G	6.59207e-05	0.00574073	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351786	GAAGAGGAACAGCCT[A/G]TGTGGGCTTCCACGG	57674
rs568375608	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259718	GAGATGGGGTCTCTC[C/T]ATGTTGCCCAGGCTG	57674
rs568391607	snp	G/T	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388809	GCCCACAGTTTCTGC[G/T]GCCTCCCTTACAGAG	57674
rs568397342	snp	G/T	2.81116e-05	0.003749	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386912	GCTGACTCCTGCCAC[G/T]GCTGCTCATTTGGTG	57674
rs568412879	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352056	GACGGGGTTTCACCA[C/T]GTTGGCCTAGATGGT	57674
rs568444457	in-del	-/TTTC			intron-variant	RNF213	GRCh38.p7	17:80279457	TTTTTCTCTTTTTCT[-/TTTC]TTTCTTTCTTTCTTT	57674
rs568445365	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320157	TTCAAAGAGAAACCC[A/G]GCCCCTTTAGCCATC	57674
rs568449462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357044	CCTGCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC	57674
rs568487954	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264034	TCCGTCCCTCGTTCA[G/T]GCCCGGCCTGAGTGA	57674
rs568490753	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80318354	TTTTGCCAGGGACCC[A/G]CCCCTGTCTGCGTAG	57674
rs568517313	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80271466	ATGAAGTGTCCAGAC[A/G]GGGGCGCAGCTGGGA	57674
rs568560474	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80341943	TCCTGAGTAGCTGGG[A/G]CTACAGGCACACGCC	57674
rs568630151	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321826	CACCTCCTGGGTTCA[A/G]GCAATTCTCCTGCCT	57674
rs568631244	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80290450	GTGTGCATGTGTGTG[C/T]GCGAGTGCATGTGTG	57674
rs568639753	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391687	AAGTCAAATCTGACA[A/G]AATTTTCCTATAAAG	57674
rs568643998	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318064	GTCAGGACGTCTTTC[C/T]GAAGTTAAACCGTCT	57674
rs568680037	snp	A/C/G	3.32167e-05	0.00407522	missense	RNF213	GRCh38.p7	17:80350369	TTGAAGATGGAATCC[A/C/G]TAGCGCCCAGCTCAT	57674
rs568696320	snp	C/G	0.000201315	0.0100308	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383062	GCTGTGATTTCTCCT[C/G]AACTGGAGGTAAGCA	57674
rs568705376	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356399	CTGCTGTTCACGCAG[C/G]ACTAGGCCTGGCTCC	57674
rs568729675	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340628	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTGAGAC	57674
rs568752744	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392152	GATTTAACTTGATGT[C/T]TTCCTGACTAGATCA	57674
rs568757273	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80310688	CTCCCGAGTAGCTGG[G/T]ATTACAGGCATGTGC	57674
rs568757818	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397744	GCCCTTCTTTAACTC[A/G/T]TGTCTGAGGGGTTTT	57674
rs568793135	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80322292	TAGCCTCCCGAGTAG[C/T]AGGGACTACAGGCAT	57674
rs568833166	in-del	-/CAC			intron-variant	RNF213	GRCh38.p7	17:80270928	ACAGTGGTTTCCCAG[-/CAC]CACCACCTCATGGTC	57674
rs568848160	in-del	-/T	0.0103295	0.0711199	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372308	AAATAAATTAGATAA[-/T]TTTTTTTCCTCATAG	57674
rs568849815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300091	CCCAGTAATGGGATT[A/G]CTGCGGTGAATGGTA	57674
rs568872957	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326436	TAGTGTGGTGCTTTT[A/G]TTACAGCTGAGAAGC	57674
rs568873504	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80299684	AGCCTAGTACCCATT[A/T]GCTATTTTTCCTGAT	57674
rs568897025	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371132	TGTGGGTCAAAAAAG[A/T]AAAAAATCTATTTAA	57674
rs568905698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331094	AAAGTGCTGGGATTA[C/T]GGGCGTGAGCCACTG	57674
rs568910763	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80279946	TTTGCAGAGGGCGAC[A/G]GCCTCCCTGCCTTCC	57674
rs568931272	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335163	CCTGACCTCAGGTGA[G/T]CCACCCATCTCAGCC	57674
rs568937796	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396394	GTATGTTCAGGCAAT[C/T]CCAATTTAGAAACAA	57674
rs568964593	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355353	TACAGGGGAAGAAGC[A/G]GGGTGAACGGGAATG	57674
rs568968988	in-del	-/AT	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386630	CCTGCTCCCTGCAAC[-/AT]AGAGCCCTAGGCCCG	57674
rs568996381	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320727	GCTCAGGCTGGACAC[C/G]GTTGCTCACGCCTGT	57674
rs569095649	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80274379	GTTCAAGGAGAATGG[C/T]TGGAAGAGAAGGGCT	57674
rs569119574	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80274647	GGGGGGTGTGGGGTG[A/G]GTGTGTGGGGTGAGT	57674
rs569120620	in-del	-/ATCCCATCTTATCTATCC	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80269723	TCTATCCATTCATCT[-/ATCCCATCTTATCTATCC]ATCCCATCTTATCTA	57674
rs569145854	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381271	TTCATTATTTTACCT[A/G]TGTCTTCATTGTAGC	57674
rs569181011	snp	A/G	4.94368e-05	0.00497152	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380894	GCGGAGAGACGTGGT[A/G]ACATGTGACCGAGGG	57674
rs569182976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310488	AAACGCCTGACCTCA[C/T]GTGATCCACCTGCCT	57674
rs569202443	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80333009	AGTTCCACCCAAAAG[A/C]GGTAAATCAGTTGTT	57674
rs569218059	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359437	GCTGAGGCGGGAGGA[C/T]TGCTTGAGCCCAGGA	57674
rs569266831	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289281	CGCTGTAAGAAGCAT[C/T]CCCTGTAGGGGTCAA	57674
rs569269128	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390423	TCTTGCCCTGTTACC[C/T]AGGCTGGAGTGCAGT	57674
rs569273475	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80265959	AGGAAGGGATCCTTC[-/A]AGTTGGGATGGGGAC	57674
rs569295005	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364156	CCCTAAAGGTGAGGT[A/G]GGACTTGACAGGCGC	57674
rs569312472	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398123	ACGGCGTGCCTGTAC[C/T]GGCACTCTGGTTTTT	57674
rs569319085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317012	GAAAGCCAACCTGGG[C/T]TGCTGTGACCGGCCA	57674
rs569333515	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283834	GCCTGATTATGTCAT[C/T]GAAGCTGCTAGAGCA	57674
rs569349819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374812	GTTGAGCTGGGTTGA[C/T]AGATTTGCTGTGTCT	57674
rs569352709	snp	A/C	0.000444704	0.0149048	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389866	ACACACCATTGCCCT[A/C]TGGCAGTTCCTGTCT	57674
rs569359002	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320430	CGATCCTGGCTCACC[A/G]CAACCGCTGCCTCCC	57674
rs569359718	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389387	GTCTCACACCGAAAA[A/G]GAAATCAGCACAGCC	57674
rs569360499	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328987	CTGCGTTAATGATAC[A/G]CTGTTTTCATTGTAT	57674
rs569382665	snp	C/T	0.00755907	0.0610114	intron-variant	RNF213	GRCh38.p7	17:80309455	GGGGAAACCAGAGAG[C/T]TGGCGCAGGGGCTGG	57674
rs569386102	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380479	CACCCATGGGATGCC[A/G]ACTGTCCTCCCAAAC	57674
rs569402462	snp	C/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80284651	CACCTGATGAGCCCC[C/G]AGCCTGTAGGTGAGG	57674
rs569405989	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338407	AAGTAATCATATTGA[C/G]AATGGTGTACCGGTC	57674
rs569439969	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263086	TGAGTCCTGGCCTTG[G/T]TCTGGTTTGATGCCA	57674
rs569440977	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344462	GAAGTTGGGTTAGAA[A/C]GTGATTTCCTGGCTC	57674
rs569468258	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368619	TGTATTTTTAGTAGA[C/G]ACAGGGTTTCACCAT	57674
rs569471551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374400	CTGTACCCGTTCAGA[C/T]GGTTCTTTGCAAGAC	57674
rs569483793	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355452	GGAATCGGGGCTCAC[A/G]GAGGAAGAGGGGTGA	57674
rs569502688	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292896	CCCTGCCCCCTGGTG[A/T]CCGGTGTCTTGGAAA	57674
rs569510571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292170	GCTCACTGCAACCTC[C/T]GCCTCCCAGGGTCAA	57674
rs569511477	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283588	CTGCTGCTGTTTCTT[C/T]CTGGCTGGCCACTCC	57674
rs569518876	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80291881	AGTGCAGGTGCCAAT[C/T]CCGCGGTACTGGACG	57674
rs569530337	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369207	AGTTCGAAACCAGCC[G/T]GGCCAACACGGTGAA	57674
rs569535309	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262518	GCAGGCACTCCTCTT[G/T]TGTGTCCCTGGGACC	57674
rs569543192	snp	C/T	0.000131781	0.00811621	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367878	TTGGATCTGTGAAGG[C/T]GAGAATTCTGAACCT	57674
rs569581599	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269516	CTATTCTATCTATCC[A/C]TCCATCCTCTTTCTA	57674
rs569594750	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278274	GGAGGTGTCGGATGA[A/G]CATGCCCGCTACAGG	57674
rs569650225	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80348893	GAGGCCCTCAGTGAC[C/T]CTGCAGAGCCACATC	57674
rs569669414	in-del	-/AA/AAA	0.440609	0.161766	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359524	GTGAGACTCTATCTC[-/AA/AAA]AAAAAAAAAAAAAAA	57674
rs569679982	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80315344	GGTGGAGGTACTAGA[C/G]GTGATGGCGGTCGTG	57674
rs569686974	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353752	TTGCATTGGGAGCTA[C/G]AGGAGTCGCCGCCGC	57674
rs569687493	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80267409	GATCACGCCACTGCA[C/G]TCCAGCCTGGCGACA	57674
rs569708056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379867	ATGCCAAAGTCCCAG[C/T]AGTCACACAGCAGGG	57674
rs569764650	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356349	CCGGGACCAGCCCTG[A/G]GTCACTGAACCTCCT	57674
rs569772770	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367533	AAGAAGAGGGAAAAT[C/T]GTAACTTGAGAATGT	57674
rs569778987	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373827	CAACATGGTGAAACC[C/T]TGTCTCTACTTCAAA	57674
rs569839121	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319101	GTAAAACAGCAGGAA[A/G]GTAAAAATGATGAAA	57674
rs569866118	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394444	ATACAAAACCAGTTA[C/T]GTTTCGGAAAGAGGG	57674
rs569893932	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352737	TTATGGTGAAGCTGT[C/T]GATGGGCATAGAATC	57674
rs569910923	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394049	GGGCATTTTGTGAGT[A/G]CCTTAAGATCAAACT	57674
rs569959554	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80342681	ATATTCTATATACTT[C/T]CATATATACTATATA	57674
rs569965991	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380777	GCTGAGAAAGTGCAG[C/T]GTGCCAAAGCGGCCA	57674
rs569993410	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80338730	GAGGCGGGCCTATCA[C/G]TTGAGGTCAGGTGTT	57674
rs569993534	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80302192	ATGGCTAGATAGGAC[A/G]AGTAAGTTCTAGGGT	57674
rs570010915	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364041	CGTAGAAAGGCAGAC[A/G]GGCTATTGTGATGCC	57674
rs570059513	snp	C/T	4.95103e-05	0.00497521	missense	RNF213	GRCh38.p7	17:80347868	ATCTGGATATCAACA[C/T]GGTGCTGGAGAAATG	57674
rs570068306	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378651	TGTATATAAGAGATA[C/T]GGAGGGAGAAAAACT	57674
rs570075668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329238	CTCACTGGCTTCCTG[A/G]GAAAAGGGCGTGTAA	57674
rs570096217	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80308079	ATCATTTGCTCCTGC[A/G]AATTTGTGACCTCTG	57674
rs570103539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297489	CCGGGCATTATGGCT[C/T]ACACCTGTAATCCCA	57674
rs570119761	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326225	GACCTCCCGGGCTCA[C/T]GTGATCCTCCTGCCT	57674
rs570126543	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261329	AACGGAAAAGTGAAG[C/T]TGCAAAAACAGACTC	57674
rs570141980	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362399	AAAAAATGGGTAAAC[A/G]TTATAAAACAACAAT	57674
rs570149734	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80293841	AAAAAAAAAAAAACA[C/T]GTGATAGGGGATTTG	57674
rs570157897	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80330870	TTGTCCAGGCTGGAG[C/T]GCAGTGGCTCAGTCT	57674
rs570164642	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80337150	TAAACTTCTCTTATT[A/G]TACTTGGGGACCACA	57674
rs570177394	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80281745	TTGTTGCCCACAGGG[C/G]GTCGGTTCCAGGACC	57674
rs570194288	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80349328	CCTCGAGGAACGTTT[C/T]GACTTGCACTGTGAT	57674
rs570240552	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277548	GGTTGCAGTGAGCCG[A/C]GATTGAGACACCGCA	57674
rs570248138	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357673	CAAAAATTATGCAGC[C/T]TTGCAAAAAATAAAG	57674
rs570277060	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80318774	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	57674
rs570283890	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287363	AAAAAATTAGCTGGG[C/T]GTAGTGATGCTCACC	57674
rs570290128	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80317532	GCGGGATTTTTCCTG[A/T]CCCCTTCGTTGGACT	57674
rs570310943	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387918	TTATGTACGGTACCA[C/T]CCGCAACTGGGCCAG	57674
rs570370591	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312662	AGGCCCGGGAGTCTG[A/C]AGGGCCCCTCTCTGG	57674
rs570382384	snp	A/C/G	0.00127913	0.0252596	intron-variant	RNF213	GRCh38.p7	17:80328299	TTGTTGCTGTATTGG[A/C/G]TTACTTTATTGGTGT	57674
rs570392956	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397551	GTCCTGTTCTGTTCC[A/G]TTCTAATTACGGGTG	57674
rs570408710	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357177	CCGCCTCAGCCTCCC[A/G]ACGTGCTGGGATTAG	57674
rs570412002	in-del	-/T	0.00874735	0.0655527	intron-variant	RNF213	GRCh38.p7	17:80328763	GCTTAGAGCCACACA[-/T]TTCTGGTCTGTGCCC	57674
rs570413591	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80335866	CCAGTAATCCCAGCT[A/G]CACGGGAGGCTGAGG	57674
rs570433932	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80296246	GCTGGTTTCGAACTC[C/T]TGACCTCAAGTGATC	57674
rs570435012	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80318577	AGAGTTTTATATGTA[A/C]CTTTTTTTTTTTTTG	57674
rs570449700	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80335269	TCCATTGATGCTGTG[C/T]GTTTCTTGGCAGCCT	57674
rs570561568	snp	A/G	1.65759e-05	0.00287883	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386441	AACAGGTTTGTGCAC[A/G]AGCCACCAGGAAGTG	57674
rs570575408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392964	ATGAGGGGACTGATT[A/G]GTCCCCTTATGTTAT	57674
rs570594413	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376467	TGGCCATTCATGCTG[C/T]AGCCGTCCTTCTGTG	57674
rs570595120	snp	A/G	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80286721	AGGTTCACACCTGCT[A/G]CCTGGCAGTTTGGGG	57674
rs570608436	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364773	AGTCAGAGCATATCA[C/T]TTAGAAGTGATTCCA	57674
rs570610787	in-del	-/C	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370722	AAATCACTCATGACA[-/C]AGCCCTGGGTTATCA	57674
rs570619202	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311080	GTGTTTAAGGAATTT[G/T]TCAGTTACTTAGGAT	57674
rs570625378	snp	C/T	0.0012739	0.0252057	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386822	GACCGTGCAGGAGTT[C/T]GATCTGGAGAAGATT	57674
rs570682092	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80299276	AGTTCTCTGTTACAG[C/G]ACATTTGGTTGGTTG	57674
rs570688658	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284125	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	57674
rs570696017	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301222	TCTTTGCCCATTCCT[A/G]TGTCTAGAATGGTAT	57674
rs570705333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294517	CTAGGATGTCTGTTT[A/G]CACGGGGCTGGCCTC	57674
rs570716145	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80266346	TTGAGCCTGGGAAGT[C/T]GAGGCTGCAGTAAGC	57674
rs570717202	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280495	GTCTCGCCCTGGGTC[C/G]CAGGCTGGAGCGCAG	57674
rs570724464	snp	A/G	1.65551e-05	0.00287702	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371985	CATCAACTGCCTGGA[A/G]GTAAGTGAACTCTCT	57674
rs570728118	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377144	AGCTGGCACTCCGCC[A/G]GCTAGATGATCCAAA	57674
rs570758064	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341910	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	57674
rs570770787	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261506	GGGGGAGTCCAGGGC[A/G]GGAGGGGAAGGAGCT	57674
rs570781363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285940	CTCGGCCTCCCAAAG[C/T]GCTAGGATTACAGGC	57674
rs570823600	snp	C/T	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391098	TAGAAAAAGCTATAC[C/T]AATGTATAAAGAGTG	57674
rs570827255	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320409	CCAGGCTGGAGTGCA[A/G]TGGTGCGATCCTGGC	57674
rs570834855	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364034	CTGGGGCCGTAGAAA[A/G]GCAGACGGGCTATTG	57674
rs570842614	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360905	AGTCTCTCTCCTCAT[A/G]AGCATATTCCTTTCT	57674
rs570870763	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322186	TTTTTTTTGAGAAAA[G/T]GTCTCGCTTTGTCAC	57674
rs570908060	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378012	GTGGACGTGGCTCTG[C/T]GGCGTGGGCTGTCCT	57674
rs570940823	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80275820	GGCACCCGCCACCAC[A/G]CCTGGCTAATTTTTT	57674
rs570949541	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374969	TGTATTCATAATTCA[G/T]ATATGCATGTGTGTT	57674
rs570972146	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376015	TATGTGGAGGAACAC[A/T]TAACCAAGCTGTTTA	57674
rs570983145	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327237	GTGAGGTGGTTCATG[C/T]GTATAATCCTAATGT	57674
rs570998073	snp	C/T	1.65108e-05	0.00287317	stop-gained, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351716	GAAATCAACAAAATA[C/T]GAGAAAATGAGGACC	57674
rs571005577	snp	C/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80275000	GTGTGTGTATGTGTT[C/G]GGGTATGTGAGTTGG	57674
rs571010705	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375563	AAAAAAGAATTAGCC[A/G]GACATGGTTGCGTGT	57674
rs571013115	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360487	GGCCAGGGATATGGC[A/G]AAATGGGGTGTGTTC	57674
rs571014629	in-del	-/CC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396745	CCCCACCCCCCCCCC[-/CC]AACCAGAGCAACTTT	57674
rs571037955	in-del	-/TAT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366847	CCAAGGTAGACATAA[-/TAT]TAAGATGTCTATACC	57674
rs571039454	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321749	TGTTTTTTGAGATGG[A/C]GTCTTGCCCTGTCAC	57674
rs571054812	snp	C/T	6.61397e-05	0.00575026	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364599	ACGGATCCACCCTTT[C/T]CCGAAAGGAAGAACA	57674
rs571054816	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80264659	GGGCCCTGCTGGTCT[C/T]CCCGCCTCCACGCTG	57674
rs571125027	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354345	GAATTGGCCTGGCCA[A/G]CGGACTTCCCTTCCT	57674
rs571137538	snp	C/G	0.0146672	0.084371	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396729	GGAAAGTGCATTTCC[C/G]CCCCACCCCCCCCCC	57674
rs571138690	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305314	CTCCCAAGTAGCTGG[A/G]ATTACAGGTGTGCGC	57674
rs571192153	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80274077	GGTGCCTTGCTGCTT[C/T]GGGGCAGGGACCTGA	57674
rs571226690	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80299580	TATTTTTAACTTCTA[A/G]GTTCAGGAGTACATG	57674
rs571231913	snp	C/T	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80345102	TGGTGACCTTCATGA[C/T]CTTTATGGCAAGAGA	57674
rs571246997	snp	C/T	0.000185615	0.00963187	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355262	TGCCAGTGATAGGTT[C/T]GCTTTGGGCCTACAG	57674
rs571251118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279429	TCTGGTTTTTGGAAG[C/T]TGAAATCCTGACTTT	57674
rs571264951	snp	A/G	0.0119091	0.0762411	intron-variant	RNF213	GRCh38.p7	17:80304615	ACTGCACTCCAGCCA[A/G]GGCAACAGAGTGAGA	57674
rs571289662	snp	A/G	0.00077993	0.0197321	synonymous-codon	RNF213	GRCh38.p7	17:80339968	GCTGCTCTGCACCCC[A/G]GCAACCACCTTTGAG	57674
rs571291484	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80311254	AGCAAAAATACGTGA[C/T]GCATGTTGAAGAAAC	57674
rs571318877	snp	A/G	0.00716266	0.059414	intron-variant	RNF213	GRCh38.p7	17:80340558	TGGGTATTCCCTGGG[A/G]GCCCCATTCCCTTCC	57674
rs571377621	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289220	GATTAGTGGCCCCAG[C/T]GGCACTGGAAGGTCC	57674
rs571393353	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320378	TGTTTTTGAGACAGA[A/G]TTTCACTCTTTTTGC	57674
rs571412060	in-del	-/TCTGCATGGCAGC	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80272736	GGGTGCTCCATGCTG[-/TCTGCATGGCAGC]TCTGCATGGGTGAGA	57674
rs571422844	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80332878	GAAGATCAAGAACTC[A/T]GGAAAGGGCAACAAT	57674
rs571427645	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385697	CTCGTCAGCCTGACT[C/T]GGCCCATCCCTGTCA	57674
rs571435656	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357969	CCGCAGTTGGCGTGA[C/T]AGAGTGAGACCCTCA	57674
rs571439403	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283807	CAGGATTCTCCGTCT[A/G]TTTCTGCCAGAGCCT	57674
rs571483976	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80270347	ACCTTGCCCTCTGAG[C/G]CAGGCTGGCCGTCTG	57674
rs571494612	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380608	ATCAATACCACACAG[C/T]GCAGCCACCTGACGC	57674
rs571534409	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80310087	CTGTCTTCCAGCTTT[A/G]ACCTTTCTGCCTCCG	57674
rs571534674	snp	G/T	0.000509137	0.0159471	missense	RNF213	GRCh38.p7	17:80317252	AGGAGTCGTTGCTGG[G/T]AGACATGGAATGGAG	57674
rs571547218	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80294234	ACCATGCCAAGGGCC[A/G]TCTGTGCCAGCTGGG	57674
rs571558451	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398688	CAGAGAGAGAAAGAG[A/G]AAGAGACAGACAAAG	57674
rs571570934	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317005	GATTCTAGAAAGCCA[A/G]CCTGGGCTGCTGTGA	57674
rs571603715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363887	GAAGACGGGCAGGTG[C/T]TCCTGCCATGGGAGG	57674
rs571629492	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326363	AGAAAGTACAGAGAG[G/T]TGTCATCTATCTCTG	57674
rs571642913	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80337570	TGGCCCGTGTTCTCT[C/T]CTTTTGTCCCCATAG	57674
rs571657452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369165	GCACTCTGGGAGGCC[A/G]AGGTGTGTGGATCAC	57674
rs571667753	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292801	TTCCCCTCGCTCCCC[A/C]TCCCTGCACAGTGAC	57674
rs571689016	in-del	-/TTTTTTG	0.0130921	0.0798413	intron-variant	RNF213	GRCh38.p7	17:80309747	CCATGGATCAGTTTT[-/TTTTTTG]TTTTTTGTTTTTTGT	57674
rs571693490	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320108	CAGATATGTACAGTC[A/G]TCACCACAGTTAATG	57674
rs571722849	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80349227	GTGATGATGTCCGCC[A/G]GGGACAGGTTTCTAT	57674
rs571739599	in-del	-/GTGCATGC	0.0611083	0.163768	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379042	CAGCAGGGCATGGTG[-/GTGCATGC]GTGCATGCGTGCATG	57674
rs571740256	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80309406	TTTCCTGGGAGGGAG[A/G]CAGGGAGTTAATGTG	57674
rs571757352	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389534	TAAACAGGACACACC[A/G]GGGACAGTAGAGACA	57674
rs571786740	snp	C/T	9.88338e-05	0.00702902	intron-variant	RNF213	GRCh38.p7	17:80343833	CGTGTCGTGTGTTTA[C/T]ACCTCGTGCGATTCT	57674
rs571787570	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384632	CAGTTTCACTACGTC[A/G]AAGATGCTTAGATCC	57674
rs571796973	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303739	TCACATGTGGCTAAT[G/T]TTTGTATTTTTAGTG	57674
rs571820101	snp	A/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80304187	TGAACCTTTATTGAT[A/T]TGTTTTTCATAACTT	57674
rs571823714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348744	CTAGGAGAAGCCCCT[C/T]GCCGATGGGGAAGAA	57674
rs571839273	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80272928	TGTTTTAGAGGTGCC[C/G]GAGGTGCGCTGACAT	57674
rs571864191	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352043	TATGTTTAGTAGTGA[C/T]GGGGTTTCACCACGT	57674
rs571877889	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80333033	AGTTGTTTCTGTTAG[A/G]GTTAAGAGGTGACTC	57674
rs571902926	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261892	TGTGGTGGCGCATGC[C/T]TGTAACTCCACCTAC	57674
rs571905353	snp	C/T	0.00358779	0.0422022	intron-variant	RNF213	GRCh38.p7	17:80271848	AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAATCC	57674
rs571908074	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379320	GAGGGATGGAAAAAG[G/T]GCTGAATACAAGAAA	57674
rs571915284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268524	TGAAAATGAATGATC[A/G]TAAGCTTAATCAAAT	57674
rs571926706	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80313327	GCTCCTGTCTACCTG[G/T]CAGGGTGGCTCTGAG	57674
rs571932753	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374363	GCTGCCTTTAAACCT[C/T]GAATGATCAACCACC	57674
rs571940882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298159	CTAGGCTGGGGGCTG[A/G]GGGAAGCCCTGTCTC	57674
rs571947437	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392620	GTTTTTTTTTTTTCT[C/T]GCTCTGTCGCCCAGG	57674
rs571958147	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383218	CAATGCTCCCCACCT[C/T]GAGTCACTCCATCCT	57674
rs571969605	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373956	TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC	57674
rs571982368	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393074	CCTCCACCTCCTGGA[C/G]TCAAGTGGTCCTCCC	57674
rs571989329	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80307285	ATTGGCCGTGACCCA[C/G]ATGTGCTGTTGTAAC	57674
rs572026860	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80277382	GCGGGTGGATCACTT[G/T]AGGTCAGGAGTTCAA	57674
rs572033323	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80302178	GTGGATACAAAAGTA[-/T]GGCTAGATAGGACGA	57674
rs572086283	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352808	CCCATTCCAGGGTTT[C/T]GGCTTCAGGGTGCCA	57674
rs572090646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80276982	GAATCACTTGAACCC[A/G]GGAGGGGGAGGTTTC	57674
rs572144784	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371481	ATGTTTTGGAAAATA[G/T]TTTAAATGTTATTTA	57674
rs572152576	snp	A/C/T	0.00358891	0.0422285	intron-variant	RNF213	GRCh38.p7	17:80278213	CAGCTTCCTGCTGGG[A/C/T]GTCTTGCTGTGAGGT	57674
rs572165338	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80275176	GGGTGAGTGGGATGT[A/G]TGTGTATGTTGGGGT	57674
rs572170854	snp	C/G/T	0.000114266	0.00755778	missense	RNF213	GRCh38.p7	17:80334226	GGCTGCAGGCTCTGT[C/G/T]CCTGAGAAAGGAGTT	57674
rs572171210	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397103	CTCAGAACCCACGAT[C/G]TTTGCCCCATCGCCA	57674
rs572181277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80296373	AGCAGCCTCTGTGTG[C/T]GCGTGTTTAGGAGGT	57674
rs572186312	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378121	AGCTAAAACCAGACA[C/T]TGACAAAGGTCCCCT	57674
rs572187647	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80312883	TCTGCCAAGGCCTGT[G/T]GTCCCTCCATCGTAG	57674
rs572205082	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287040	TAGAGGTGCATAAAA[C/T]GTGGAAAGCCTGTGT	57674
rs572231687	snp	C/G	8.24559e-05	0.00642037	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361741	CTCTGCAGGACTGCC[C/G]AAGAAGTTCGTGGAC	57674
rs572258312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357416	GCCCATCTATCCATC[C/T]ACCTGTCTATCAGAC	57674
rs572261923	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80275342	TGGAACTCTGTCAGA[A/G]TGGGAAAGTGGCAGT	57674
rs572276808	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387626	TTCTTCAGTCCACGG[C/T]CTAAAACCCACATCT	57674
rs572279673	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295272	GGAACGGGGCACCCT[C/T]TGTCACTGCACCTTT	57674
rs572289074	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80297226	GGAGGTCGAGGCAGG[C/G]GGATCACAAGGTCAG	57674
rs572295345	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351414	AGGGTTTCTGGTCAA[C/T]GAAGGAATGCCACTT	57674
rs572322791	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352468	AGAGTGGCGGGGGTC[A/G]GACTATCTTCAGATC	57674
rs572327488	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280578	CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	57674
rs572354288	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292681	TCTCTCGGGGGTCCC[C/T]CACCTGGGTTCTCTG	57674
rs572373593	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265987	GACATGGGAAGCCCA[C/T]GGCCAGGCTGGAGAC	57674
rs572380913	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376804	GTTCCCTTTCTTCCT[C/G]TAGGCCTCCTGCTGA	57674
rs572405717	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272320	TAAAAAAAGAAAAAG[A/G]AAAAAGAGGTTTATT	57674
rs572415185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384628	GATGCAGTTTCACTA[C/T]GTCGAAGATGCTTAG	57674
rs572444299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80335571	TTGGTTTCTTTTTGT[C/T]TAAATGGTAATGTTG	57674
rs572444597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322555	CACTCCGGCCTGGGC[A/G]ACAGAGCGAGACTCT	57674
rs572450404	snp	A/T	0.145305	0.227022	intron-variant	RNF213	GRCh38.p7	17:80276085	TTTATTTATTTATTT[A/T]TTTTTTGTTTTATTT	57674
rs572484090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341507	TATTAGCTAGTCACT[C/T]AACACATAATGACAT	57674
rs572494891	snp	A/G	0.00914312	0.0669923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370124	AGGGACCACAGTGGC[A/G]TGAGGGACATGGAAC	57674
rs572494898	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355610	TACAGGGGAAGAAGC[A/G]GGGTGAGTGGGAATG	57674
rs572494959	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360618	TCTCAGAAGGCACGA[A/G]CGCCTGGAGCATCCC	57674
rs572531379	snp	A/C	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360293	AGATGGGTGGCTAGA[A/C]TTGCAAGGTGAATTT	57674
rs572531816	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358558	GCTCTCCCAAGTGCT[C/G]GGTGAAACGCAGCCC	57674
rs572553502	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386982	GAGAGGGAAGCAGCA[C/G]CTCACCCTGCAGTCT	57674
rs572554255	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259863	CTGTCGAGGATGTTG[C/G]ACTAATTGTTGGCGA	57674
rs572566569	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351454	GGACACAGGAATGGG[G/T]AAGAAAACGAGCCGC	57674
rs572575520	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351857	TTTATTTATTTATTT[G/T]TATCTATTTATTTTT	57674
rs572577861	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259297	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	57674
rs572578688	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80301240	TCTAGAATGGTATTG[C/G]CTAGGTCTGGGCAAA	57674
rs572590471	in-del	-/ATGCCTG	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80333429	TGGGCACAGTGGCTC[-/ATGCCTG]ATGCCTGTAATCCCA	57674
rs572599160	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80335999	AAAAAAAAAACTACA[A/G]AAGATTAGGTGTTCC	57674
rs572611641	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80295144	TTTTCTCCTACCACT[-/G]TCTCTTGGGATTTCT	57674
rs572614465	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273597	TGGGTTCCAGACCCC[C/T]TGGGGCCTCCACCGT	57674
rs572618890	in-del	-/A	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379010	AAACCCCGTCTCTAC[-/A]AAAAAAACACAAAGC	57674
rs572624505	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384714	TCTGGGTCTCTTCTT[C/T]CAGCAGCTTCTCTCC	57674
rs572630851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80265107	GCTAGAGAGCAGTGG[C/T]GAAATCTCAGCTCAC	57674
rs572701206	snp	A/C	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345668	GGTACCAATGCTGAC[A/C]CCATAAAGCTGGTCA	57674
rs572713059	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381945	GCCCAGAGGCTGGAA[G/T]GAGCTGCTCTGTTCC	57674
rs572735313	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383126	AGAAAGGAAGGGTCC[C/T]GGCGTCTGCTGAATG	57674
rs572745215	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80285336	GGAACTCAGGCAGGC[C/G]CTCTAAACCCAGCCC	57674
rs572749770	snp	C/G/T	0.000114136	0.00755346	missense	RNF213	GRCh38.p7	17:80327891	CCGACTCTGTGTTGA[C/G/T]GAAAGTTGTTGGTGA	57674
rs572761456	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80289996	ACTTAGGAGGTGGAG[A/G]GGGGTGGGCACCTGT	57674
rs572769798	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80329376	AGTTTCAATGTGCTG[C/T]GCCATCATTGCCTCC	57674
rs572787188	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80275964	CCATGCCTGGCCAGT[-/TT]TTTTTTTTTTCTTTT	57674
rs572853616	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326217	TAAGCGCTGACCTCC[C/T]GGGCTCACGTGATCC	57674
rs572875107	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396116	CTTTGAGACCTGACT[A/G]AAAAAATTAGGTGTG	57674
rs572890790	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80282693	GTGAGCCACTGCACC[C/T]GGCCTATTATTACTA	57674
rs572893285	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296200	AATTTTTGTATTTTT[A/G]GTAGAGAAGGGTTTT	57674
rs572927018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285763	GCAGCCTCTGCCTCC[C/T]GGGTTCAAGCAATTC	57674
rs572947701	snp	C/T	0	0	intron-variant	RNF213	GRCh38.p7	17:80270207	TAGTGGAGGACGGAC[C/T]TCAGCAGCCTCCCTG	57674
rs572948124	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391271	ATCATCCTCTGAATT[A/G]CCTTTATGTTTTATT	57674
rs572959504	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80333377	GTCTTCTGCTTCTTA[C/T]GTTTTTAGGTAGACC	57674
rs572971002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80269800	CCTATCTACCTGTCT[A/G]CCTACCTACCTACAT	57674
rs572977296	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352120	AGCCTCCCAAAGTGC[C/T]GGGATTACAGGTGTG	57674
rs573036464	snp	A/G	1.65015e-05	0.00287237	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369485	ATCCACCTGTCTTCT[A/G]TTTCTCGTGTTCTAA	57674
rs573040638	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80305473	GTGAGCCACTGCGCC[C/T]GGCCTGATTTTATTA	57674
rs573054101	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321913	GTATTTTTGGTAGAG[A/G]CGGGGTTTTGCCGTG	57674
rs573060988	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80266904	CTAGGCCTCTTGCAC[C/G]AAATGGTTAGCCAAG	57674
rs573061775	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80293759	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	57674
rs573113260	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324659	TTTTTAAAAGAATTA[C/T]GGTTTAGGAACATAA	57674
rs573118215	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375657	GCAGTGAGCCGAGAT[C/T]ATGCCACTGCACTCC	57674
rs573135549	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394734	CTTGAGCAGCGCCGG[C/T]AGGAGGCACGGAAGG	57674
rs573148375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80273808	TGTATTTAGTAGAGA[C/T]GGGGTTTCACCATGT	57674
rs573148940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80294263	GGCAGCCTGCACCTT[C/T]CTCCAGGGGCTGTGT	57674
rs573171787	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395260	AAAAAAAAATGAATT[G/T]TATTTTACTTGTCAC	57674
rs573176027	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320445	GCAACCGCTGCCTCC[C/T]GGGTTCAAGTGATTC	57674
rs573180592	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355068	TATCTTGGATGTGGC[C/T]GTGTATTGAGGAAGG	57674
rs573217021	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80304808	TGTGTAGCCGTCAGC[A/G]CCATCCACCTCCCGA	57674
rs573218709	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320120	GTCATCACCACAGTT[A/C]ATGACAGAGCATTTT	57674
rs573230171	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309842	CTTACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG	57674
rs573252320	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280092	CAGGCATGCTCTTTC[C/T]TCTGTGGGCTGGGGC	57674
rs573277585	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80284734	CACTGAGCCTCTCAT[C/T]AGCTGTTTCCCGTTA	57674
rs573288928	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80298218	GCGCGGTGCTCCTCT[A/T]GCTCTGTGTGCACGG	57674
rs573312676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80326160	GGTCTTCTCTGTTGC[A/G]CAAGTTAGCATGTAG	57674
rs573350269	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80303831	CGCCTCAGCCTTCCA[A/G]AGTGCTGGGATTACA	57674
rs573355576	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375251	ATTTCAGGAACTTTG[A/T]AGCCCAAAAGTTGCT	57674
rs573391180	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380651	CGGGTCTGGTCCACC[A/G]GAAAGGCGAGTCTAT	57674
rs573395472	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288524	CTCCACTGGGGATGC[C/T]AGCCCACCCTGTCCC	57674
rs573411230	snp	A/G			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389271	AGAAGTCACTCTGGG[A/G]TTTCTGAGCACAGCT	57674
rs573434402	snp	C/T	0.000399281	0.0141238	stop-gained, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354545	AGGGAAGCCTGCAAC[C/T]AGGACGCTCTCCAGG	57674
rs573447268	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80347566	TGGTTTCCCCAAGGA[C/T]CAAGAGTACACCCAG	57674
rs573467672	snp	C/T	3.29451e-05	0.00405851	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389939	CTGGTCTCTTCCTCT[C/T]TGCTGGACAGAGGGA	57674
rs573486009	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378015	GACGTGGCTCTGCGG[C/T]GTGGGCTGTCCTGTG	57674
rs573504573	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80282819	TCTCCTGCCTCAGCC[G/T]CTAGAGTAGCTGGGA	57674
rs573504759	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363945	ATTTGCCGAACCCTT[A/C]GTGAGTGCCAGGCGT	57674
rs573507752	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389621	GAGGCCCCTGCAAAC[A/G]GCGTGATGTGAGCGG	57674
rs573538366	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359599	AAGAGAAAGAAAGAG[C/T]GAGAGAAAGAGAGAA	57674
rs573577494	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379521	ATCTGAGGGTGCTCA[A/C]GTCTGCCGGTGATAA	57674
rs573580511	in-del	-/T	0.000165404	0.00909256	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360054	TCATCCCTCACCTTA[-/T]TTGCAGACATAAAGG	57674
rs573604816	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356833	TTGCCAGGTTCCTCT[C/G]TACTATATATTTAAA	57674
rs573616031	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384326	CCTAAGCATCGAGGC[A/G]TACGTGGAAGACGGG	57674
rs573620548	in-del	-/C	0.0836354	0.186609	intron-variant	RNF213	GRCh38.p7	17:80281277	CACACCACTCACACT[-/C]CCCCCCCACACACAT	57674
rs573623063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374156	GGGTTTAGAGTTGAC[A/G]TGACTTGAGCCACCC	57674
rs573625463	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369241	CCATCTCTACTAAAA[A/T]TACAAAATTAGCCAG	57674
rs573629946	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278318	CCTCCGCCTCTAGGG[C/G]CTTGGGAGGCCTGGC	57674
rs573642434	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80332509	ATCAAGGACCGAGTC[A/G]AACAGATCAAGGAAT	57674
rs573656976	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374472	GGGGCTGCGGCAGGA[C/T]CACCCAGGCCAGATG	57674
rs573682272	snp	G/T	1.6522e-05	0.00287414	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368161	ACAACACCCTTTCTC[G/T]CAAGAAAGCATCCTT	57674
rs573695825	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363029	GGTTTTCCAATAGTT[C/T]GGATTTCCCACGGGG	57674
rs573697031	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80268217	TGGTGGATTCCATAT[C/T]TTGGCTATTGTGAAT	57674
rs573706674	snp	A/G	0.000127771	0.00799182	intron-variant	RNF213	GRCh38.p7	17:80332002	TTTCTTTTCGCTTCT[A/G]AAGTGGACTTTGGAG	57674
rs573732835	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362456	ATCCAGGAAACATTT[G/T]AAAAATTGCTTAGCC	57674
rs573738914	in-del	-/TGAGT	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80301487	CTAAAAATGGACAAA[-/TGAGT]TGAGTAGTCATCTAA	57674
rs573740453	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353777	CGCCGCTGTGCAGGG[G/T]TGAGGATGGCGCCCC	57674
rs573755881	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80348377	TTCTTCCCCAGGCAG[C/T]GGTTAGGGATCCTGC	57674
rs573763625	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80282341	GGCTGAATCTGTGGC[G/T]GCAGAGGGCCGACTG	57674
rs573764810	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262628	CCTTTATAGCCTTTT[A/G]CAAAAGGATAGCTTC	57674
rs573806463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338584	AGCCCAGGAGTTCAT[A/G]ACCAGCCTGGGCAAC	57674
rs573821057	snp	C/T	0.0652144	0.168387	intron-variant	RNF213	GRCh38.p7	17:80313642	AGGTGATGGTGGTGA[C/T]GGTGATGGTTGTGGA	57674
rs573826812	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80262086	TTGGAGAAGGAAACA[C/G]TTCGGGTGGAAAGAA	57674
rs573863090	snp	A/T	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80342745	ATATTATATATATAT[A/T]GTATGTATATATATA	57674
rs573884997	snp	C/T	0.000538199	0.0163954	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288408	GTGGCACTGAGCCCT[C/T]GGCACCTGGGCTCTG	57674
rs573898137	snp	A/C	1.65288e-05	0.00287474	missense	RNF213	GRCh38.p7	17:80347974	GAGGCACAAATACAG[A/C]CCCTCTGACGTCTTC	57674
rs573909784	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80272786	GGCAGAGCAGCTGGG[C/T]GGGCAGATGCCTTAG	57674
rs573979816	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RNF213	GRCh38.p7	17:80260898	GGCGAGCTCGGGGGC[C/G]GCAGGTGCGAGCGGG	57674
rs573984771	snp	A/C	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393166	TTGTATTTTTGCTAG[A/C]GACAGGGTTTCGCCA	57674
rs573993191	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80316394	AAACAGTTGGCCTGA[A/G]CTTTTCAAAACTGTC	57674
rs574034324	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80324246	AGATGCCCTTTATCA[A/G]TTTGTGGAAGTTCCT	57674
rs574040932	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260046	ATTTTAAAACGGAGG[C/T]CCCTGGTCACACCAT	57674
rs574116086	snp	A/G	0.000399281	0.0141238	missense	RNF213	GRCh38.p7	17:80336253	GCCTGCTTCCATGAC[A/G]CTGTGCAGGGCTACG	57674
rs574138617	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80296726	CTTACTCTGTTCCCC[C/T]AGTCTGGAGTGCAGT	57674
rs574144994	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80277085	AACCAAAAAAAAAAC[-/A]AAAAAAAGAATACGA	57674
rs574193759	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372282	TTTTATATCCAAAAT[A/T]TTTATAATGTAAATA	57674
rs574194266	snp	C/G	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80271760	GAGGTGGGCGGATCA[C/G]GAGGTCAGGAGTTCA	57674
rs574195360	snp	A/C	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80324754	AAATGTAGAAACTGG[A/C]AGCCAGAAGGAAGGA	57674
rs574247407	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367157	AGAAGCCTTTATACA[A/G]CGTGGTATCATTGAT	57674
rs574324065	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397054	CCTGTGCCCTGAAGC[A/G]CAACAGAACCTCAAC	57674
rs574331177	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387608	CTGGTGCCCACCTCC[A/G]GGTTCTTCAGTCCAC	57674
rs574333858	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80301661	GCCAGTGAGGATGTG[C/G]GAAAGAGAAACTCTC	57674
rs574358958	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352444	GATACGCCTGTTTGG[C/T]GGGGAGGGAGAGTGG	57674
rs574367887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80322964	CCAAATCCTAGGTGA[C/T]GAAGATTTACTCCTA	57674
rs574373417	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351957	TCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	57674
rs574388349	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80311804	CTCCTGACACTTGCA[C/T]GATGTGCGGGGCTGT	57674
rs574397174	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357253	ACAAGAATTTTGAAA[C/T]AGAGCTATTATTGTT	57674
rs574467507	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80317353	CATTAGCGACAGCCA[A/G]GAGATCTCAGCAGTG	57674
rs574477244	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312372	CTGGTCTGGTGGGTC[C/T]GGCACGGAGGCGGGG	57674
rs574491108	snp	A/G	0.00993419	0.0697739	intron-variant	RNF213	GRCh38.p7	17:80281072	TCACCCCAGTCACAC[A/G]CACCCCCCGCCACAC	57674
rs574519089	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306031	GACAGGGCCTCACTA[C/G]GTTCCCCAGGCTGGT	57674
rs574543715	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300673	ATTGTCCTGCCTCAG[A/T]CTTCTGGGTAGCTGG	57674
rs574548388	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80307256	GCCCCCGGGGGCTTC[C/G]TCTGACCCCTATAAT	57674
rs574549091	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259283	GACCACCCTGGCCAA[C/T]ATGGAGAAACCCCGT	57674
rs574558485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384956	TACAAATACAAGTCT[C/T]GCAGCCAGTCTCAAA	57674
rs574564801	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80293042	GAGTATATATTTTTT[C/T]GTTTTTGTAAACATA	57674
rs574604785	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356708	CAGCGCTTGTCCCAG[C/T]GCCTGGGTTTTCCTT	57674
rs574636912	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320756	GTAATCACGGCACTT[C/T]GGGAGCCCAGGAGTT	57674
rs574649912	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80386117	CTCTATCAGCATATG[A/G]GATGGGGCAGAACCG	57674
rs574652103	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360762	AAAACCAACGACAAC[A/G]CAACACTTTTACAAA	57674
rs574682472	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392487	CCGTGGGCTTCTGTC[A/G]TGTTTGTGTACTGCA	57674
rs574685129	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361167	CTAGATGTTTCTCTT[G/T]GGGGCTAGCTTGGCT	57674
rs574692929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285209	CCTCAGTGATGCTCT[A/G]ATGTGGACACATCTG	57674
rs574695062	snp	A/C	4.96849e-05	0.00498397	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384989	CTGTAACCCCAATAA[A/C]ATTTTTTAGGTAAAT	57674
rs574708047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340865	ATTGGAGTACAGTGG[C/T]GTGATCTCGGCTCAC	57674
rs574748023	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361669	TCACTCCGGAGCCCC[C/T]TGGAGGCAGGGGAGC	57674
rs574774664	snp	C/T	3.29669e-05	0.00405984	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381516	TACAAACCAGATCCC[C/T]GCTGAACACTCTGTT	57674
rs574787371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376274	TATTCTTTGATACAT[C/T]TTAATGTTAAGTTTT	57674
rs574812487	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386514	ACAAGCAAGCTTCAG[C/G]CCCTTCCCTAACAGA	57674
rs574812727	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381129	AATATACAAGTTATA[C/T]ATCTTCATGTTTCCC	57674
rs574818333	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80280144	CAGCTCCTGGGAAAT[G/T]CAGGCAGCGTCCACA	57674
rs574834718	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357397	TCCACCCATCTGTCC[A/G]TCCGCCCATCTATCC	57674
rs574846436	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371395	CAGGGCAGGCAGGCC[A/G]CTGACTTCCAGGAGC	57674
rs574885207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376596	ACACCCCCCAGAGCT[C/T]GTCACTGTAGAGACC	57674
rs574892891	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364697	GGAAGGTGATTTCAT[C/G]ACTAGGCCATTACAT	57674
rs574896479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80317447	ATAGTCTGTCCCTAG[A/G]AGAGCGCTTCGGAGT	57674
rs574901812	snp	C/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80270357	CTGAGCCAGGCTGGC[C/T]GTCTGGAGGACAGAT	57674
rs574925933	snp	A/G	0.000132979	0.00815302	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369883	GTAAGAACAACATGG[A/G]GACTTGCTTCTGGAA	57674
rs574930164	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364345	GACCCCGGGTCCCGC[A/T]TCTCTTCTCCCGTCT	57674
rs574955503	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355569	GGCTTATGGAGGAAG[A/C]AGCGGGGTGAGTGGG	57674
rs574960086	snp	A/G	0.00199481	0.0315187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356065	GGAGTGCAGTGATGC[A/G]ATCTCAGCTCACTGA	57674
rs574962686	snp	A/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80284820	AGGGGACAAGACAGC[A/G]CCTCCTCTGGTGATT	57674
rs575014195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80341428	TATCAACAGTACCTC[A/G]TCCTGTTGGGATAAA	57674
rs575017224	in-del	-/CCAC	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80296261	CTGACCTCAAGTGAT[-/CCAC]CCACCTCGGCCTCCC	57674
rs575017683	snp	C/T	0.0134861	0.0810011	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368556	TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT	57674
rs575031878	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286407	TGTGGCCATGTGTGA[C/T]AGAGAAGGGGTTGCA	57674
rs575034417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264946	GGGCGGCCTGGCTCC[C/T]TCCTTCCCCTCTTTC	57674
rs575046346	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269448	ATTCTATCTATCCAT[C/T]CATCTATTCATCCAT	57674
rs575052394	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354797	CTAATTTCGTGTTTA[C/T]AGTTTTTCATACTAA	57674
rs575055295	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80310672	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG	57674
rs575064991	snp	A/G	6.58903e-05	0.00573941	synonymous-codon	RNF213	GRCh38.p7	17:80345220	GCCCTTCTCCCTCCG[A/G]AAGAGGTGGGAGTCG	57674
rs575067800	in-del	-/A/AA	0.488485	0.0749998	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377437	AAATATGCTCATGAC[-/A/AA]AAAAAAAAAAAAATC	57674
rs575080275	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394342	TATGCCAAATAAACA[C/T]GCAGTCTCAGTGTGC	57674
rs575095952	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387370	CTAGGCCTCCCAAAG[C/T]GCTGGGATTATAGGC	57674
rs575103720	snp	C/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280560	CTGGGCTCAAGCAAT[C/G]CTCGTGCCTCAGCCT	57674
rs575153111	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80294070	TTTGTAGGTCTTCAC[A/G]TGGCCTCTGACCCTG	57674
rs575175300	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359768	TATCAAAGCCAGACA[A/G]GTTCAGGAACCAGAA	57674
rs575193139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262846	GCAGGGAGGGGGCCT[A/G]AGTGTCCTCCTGGCT	57674
rs575211485	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354671	TCCGGGCCATGGGGA[C/T]TGAGCTGTTTCTTTC	57674
rs575219765	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395936	TCCGCCATGGATGCC[A/T]CATCACCAACCCTGA	57674
rs575248053	snp	A/G	8.24083e-05	0.00641852	missense	RNF213	GRCh38.p7	17:80345779	CAACATCAGTTGGAC[A/G]CCATCTTGTTTTTTG	57674
rs575361166	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80338704	CATCATGGTTCACAC[G/T]TTGGGAGGCCGAGGC	57674
rs575362379	snp	C/T	0.00676609	0.0577691	intron-variant	RNF213	GRCh38.p7	17:80273649	TTTGAGACAGAGTTT[C/T]GCTCTTGTTGCCCAG	57674
rs575376200	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80349533	CTCTGGGGAGGAGAG[A/G]AAGGCACCCTCGGGG	57674
rs575395176	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380622	GCGCAGCCACCTGAC[A/G]CTGAGAATGCGGTCG	57674
rs575404986	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80331928	AGAGAAGTGAGGAGA[G/T]AAAGTCTTAGGAAAG	57674
rs575427186	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80327369	GCCAGGCATGGTGCT[A/G]TGCACCTGTGTTCCT	57674
rs575440061	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80333351	AGGCGTGAGCCACCG[C/T]GCCCGGCTGAGTCTT	57674
rs575440594	snp	A/C	4.29489e-05	0.00463385	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374685	TGCAGGGTGATGGAC[A/C]ACTGATGCAGCCCAT	57674
rs575456279	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375206	TCATTAAGCTGGCTG[C/T]TAAATATGCGTTGAG	57674
rs575508780	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320113	ATGTACAGTCATCAC[C/G]ACAGTTAATGACAGA	57674
rs575568195	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80325470	GCCCTTGAAACAACC[C/T]TTCTGAAAGTCCCCT	57674
rs575570715	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373874	TGGACATGATGGTGG[A/G]TGCTTGTAATCCCAG	57674
rs575571878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359026	CATGGCGTGACACGG[A/G]GACAGTGCGCTGCGA	57674
rs575583144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80278501	GCCTGGCAGGGTGCC[A/G]CCTCTGGTGTGGGCA	57674
rs575599513	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392451	CTAAAGTCATGTGAA[C/G]GGGCCAGCACAGGGC	57674
rs575624537	snp	A/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80304658	TAAATAAATAAATAA[A/T]TAATAATAATAATAA	57674
rs575652855	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80264384	GTGGAGAGACAGGAG[C/T]GGGGCAGTGTCAGGC	57674
rs575674090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80316697	GCCCAGGTATGTAGT[A/G]GCAAGGTGCCATGAT	57674
rs575674246	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80279136	GTGAATTTCAGCTTT[A/T]TTGTGCTTGCCCTTC	57674
rs575685388	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80303794	AGGCTGGTCTTGAAC[C/T]CCTGGCCTCAAGTGA	57674
rs575698192	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80283994	TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA	57674
rs575710441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80283467	TGCAGTTGCGTCTGC[A/G]CTTACTGCAGTCTTT	57674
rs575730376	snp	A/G	0.000329457	0.0128304	intron-variant	RNF213	GRCh38.p7	17:80349761	AATTTGCATTTCTTA[A/G]CTCTGTAGATCACCA	57674
rs575747287	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303237	TCCTTCCCCTAGCCT[A/G]GAGGCTCAGGCCACA	57674
rs575787008	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369353	CAGTGAGCGGAGATC[A/G]CGCCACTGTACTCCA	57674
rs575791328	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385305	TAAGCCCTTACCATG[C/T]GGTGAAGGGTGCTTG	57674
rs575809777	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366631	ACACATCACTTCCAA[A/G]TAAGATTAATCCCAG	57674
rs575830763	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324816	TGTGTGTCTTCACAT[C/T]TCTGGTGCTGGACAC	57674
rs575837232	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292005	CTCTGGGTTGTGTCT[C/T]TGGTTGGTTAAAGAT	57674
rs575853541	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358778	GCTGGGCGTGGTGGC[A/G]CGTGCCTGTATTCCC	57674
rs575861755	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394262	AATTGTGAGAGAAAC[C/T]AGATGACTGTAAACT	57674
rs575892201	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319819	GCAGGCAATGCCACA[C/T]GAGGAAGCTCCCTGC	57674
rs575909649	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388490	GGGCGCTCTTAGCCA[A/G]GGGATACACAGGGCA	57674
rs575960715	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80343407	ACTCCTCCCCGTGTA[C/T]AGAATTCCTTGTTTC	57674
rs575962444	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80277803	TCTAAGCGCAGACGC[C/T]GCATTCTAACCATGG	57674
rs575965108	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363927	CTCACCCGTTCACTC[C/T]GCATTTGCCGAACCC	57674
rs576003630	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389120	TCTTACCAGGTGGTG[A/G]GATGCCAGAAACCCA	57674
rs576024127	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366947	TATTGCCTAAAAACC[A/G]GTGTTTCCACTTCTA	57674
rs576030923	snp	A/C	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373999	GATAGAGCGAGACTC[A/C]GTCTCAAAAAAAAAA	57674
rs576058424	snp	C/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80272720	GTGGGGCTGGCAGAG[C/T]GGGTGCTCCATGCTG	57674
rs576063930	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80261547	GGTGGTGGCCCTTCC[C/T]TGCCCCCACCTTGTT	57674
rs576067703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379484	GTTCTCCACCCACCC[A/G]AAACAAGCACACACT	57674
rs576094279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291551	TTATAGCTTTGCACT[C/T]CATGCTACGTTTGAG	57674
rs576099027	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373371	GGTGCCACTGCTTCC[A/G]CGTTCCGCCTGCCCT	57674
rs576113500	snp	C/T	0.000811117	0.0201221	intron-variant	RNF213	GRCh38.p7	17:80348305	ATTGTCTTTCTGCAC[C/T]TGTACCCTATCCCCT	57674
rs576121603	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80272387	TGGCCCTGATGTCTG[A/G]TGAGGGCTTTTGTGC	57674
rs576133339	snp	C/T	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80337319	TCCACAGATGTAAGT[C/T]AAGTGCCCCCATGTG	57674
rs576204636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357885	CCTGTCTACTTGCAC[A/G]GCTGAGGTGGGAGGA	57674
rs576242513	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80313539	AAGGTGATGGTGATG[A/G]TGGACGTAATGGAGG	57674
rs576243165	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80268200	GTCCATTGTTGGATA[C/G]TTGGTGGATTCCATA	57674
rs576246171	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352309	AAAACATGAATCCTG[G/T]GATGGGAGGCTGCGT	57674
rs576251088	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381819	CACCCCACACACAGC[C/T]AGTCTGAGCTCTGTC	57674
rs576274857	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80280841	GAGAAATGGATGGGA[G/T]ATTTATAGTAAAGCT	57674
rs576302583	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372249	TGGGGACATTATGGA[C/T]ACTTTTTATCTTCAT	57674
rs576305525	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80318104	AGTCCAGCCATCCCT[C/T]TGAAGTCAAGTCACC	57674
rs576327507	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336739	TTTTTTATCAGAAAA[A/G]AGTAAACATTTAAAA	57674
rs576339856	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80297072	CAGAGTTAGTGCCGG[A/G]GCTTAAAGTATGAGG	57674
rs576349137	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF213	GRCh38.p7	17:80259883	ATTGTTGGCGACCCC[C/T]CGCCCCAAGCAGGAG	57674
rs576356118	snp	G/T	1.64768e-05	0.00287021	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361813	CCATGGAGAGCCGCA[G/T]CAGGAACTTCTTCAG	57674
rs576361705	in-del	-/TGT	0.00279162	0.0372561	intron-variant	RNF213	GRCh38.p7	17:80337405	CTGAGTGACAGATCA[-/TGT]TGTCAGGGTGGCACC	57674
rs576363660	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309690	TGATGGCAGGATGAC[C/T]CGGCTCCTCCGTCCC	57674
rs576366509	snp	C/G	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80312672	GTCTGCAGGGCCCCT[C/G]TCTGGGGCGTGCTTT	57674
rs576378293	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80271703	AAAAGAAAAGGCCGG[A/G]TGTGGTGGCTCAAGC	57674
rs576387305	snp	A/G	0.000232829	0.010787	synonymous-codon	RNF213	GRCh38.p7	17:80339767	CTGCCTCGACCTAGA[A/G]ACCCTTGGCCACTGT	57674
rs576393976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336103	ATTACTGCCCAAGAC[C/T]GAGTCTTGTGCTATC	57674
rs576419449	snp	A/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287505	AGACCTTGTCTCAAA[A/T]AAATAAATAAATACA	57674
rs576423779	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80296475	GCCCCTGCCTGTGCC[A/G]TGTCTAGTTCAGGAA	57674
rs576442028	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362324	TTAAGAACATCCTTA[C/G]AGCTAATATGACTAG	57674
rs576448677	snp	C/T	0.000462726	0.0152036	missense	RNF213	GRCh38.p7	17:80348063	GTCCCCGGGCCTTGA[C/T]GGAGGAACTTCACCA	57674
rs576461966	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	RNF213	GRCh38.p7	17:80260433	CGGCGCGCAGCGGCC[C/G]GAGGCGCCTCCCGGG	57674
rs576466600	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331893	GAAATCCTAGCAGCT[A/G]TGTGCTCTTGAGTTC	57674
rs576496874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80323193	TCAAAAATCTGTTGA[C/T]GATACATGTATGGAT	57674
rs576524065	in-del	-/TC			intron-variant	RNF213	GRCh38.p7	17:80310176	ATTCCTTCTTTCCCG[-/TC]TCTGTGCAGTTTTCA	57674
rs576544393	in-del	-/C	0.0162398	0.0886349	intron-variant	RNF213	GRCh38.p7	17:80301465	AAGTGAACAGAAAAA[-/C]TCAGATCTAAAAATG	57674
rs576560662	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80324732	ATGATATGAAAGTCC[-/A]AAAAAAAAATGTAGA	57674
rs576581384	in-del	-/CTTGAAT	0.00119737	0.0244387	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369085	GGGTGAGAGGAGTGA[-/CTTGAAT]CTTGAATCTTTCAAT	57674
rs576598523	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80334783	AGGCGACCGCCACCA[C/T]GCCCGGCTAATTTTT	57674
rs576642098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330127	TATTTAATGTAGAGG[A/G]ATTCTTTTTCTCGGA	57674
rs576650421	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80266755	GATGCGCCCACCTTG[A/G]CCTCTCAAAGTGCTG	57674
rs576681710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80300942	GTATGTCTTCTTGTG[A/G]AAAGTGTCTGTTCAT	57674
rs576724746	snp	C/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80317876	CGGTGGGTCCCAAGC[C/T]CTTGTCCAGCATCCA	57674
rs576729785	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80322392	CCATCCTGGCTAACA[C/G/T]GGTGACACCCTGTCT	57674
rs576756070	snp	G/T	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80306795	AGGCGGAGCTTGCAG[G/T]GAGCCGAGATCACGC	57674
rs576756131	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80312298	AGGAAGAGGAAGGCA[A/G]GGGAGAGAAGGGAGG	57674
rs576759304	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80328164	TCTCAAGAACATCAC[A/G]GGAAAGTGATAAAAT	57674
rs576764779	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356660	AGCGGCTCCAGATAG[A/G]GCGGAACCAGGCTCG	57674
rs576781049	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80300795	GACCTCAAGTGATCC[A/G]CCCACCTTGGCCTCC	57674
rs576850432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381991	CCTGGCTAAGACCTG[C/T]GGTATTCGGGAGCGT	57674
rs576871783	snp	A/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80310559	CACCCAGCACAATTT[A/T]TTTTTTTTTTGAGAC	57674
rs576995295	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80311695	CTCTCGGGCAGCCCC[A/G]CCCAGCAGCAGCCTT	57674
rs577000360	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364883	ACCCCAGAACAGACC[A/C]CTAGCCTGGCCATCT	57674
rs577010400	snp	A/G	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80300242	AATAGCAGCCATTCT[A/G]ACTGGTGTTAAGATG	57674
rs577030013	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396570	GGGGAGGTGGCTGGA[C/G]AAAACCTGAGCCTCG	57674
rs577031372	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80289488	CCAGCTACTCGGGAG[A/G]CTGTCGCAGGAGAAT	57674
rs577038950	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396216	GCAGTGAGCTATGAT[G/T]GCACCACTGCACTCC	57674
rs577038989	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80282556	GGCGCCCACCACCAC[A/G]CCCAGCCAATTTTTT	57674
rs577040275	snp	G/T			missense	RNF213	GRCh38.p7	17:80347081	ATAGAGAGCGCCAAG[G/T]GCATCTGCTCCTCAG	57674
rs577062164	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321925	GAGACGGGGTTTTGC[C/T]GTGTGGGTCATGATG	57674
rs577069538	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396960	TAAAAAACGCCTTCA[C/G]CCCTGCTGTGCTTCC	57674
rs577098592	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390785	AAAGCTATCCTAGGC[C/T]GGGTGTGGAGGCTTA	57674
rs577105072	snp	G/T	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80310264	TGATCATTTGTTTGT[G/T]TTTTTGAGATGGAGT	57674
rs577109712	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80282849	ATTACAGGTGTGTGC[C/T]ACCACGCCTGGCTAA	57674
rs577143392	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370767	TCATGGACCGCCACC[C/T]GTGCTGGGAGGAAGG	57674
rs577152218	snp	C/T	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80345711	GAACAACTGCAGACA[C/T]GATCTACTCCAGAGT	57674
rs577169974	snp	G/T	0.000115499	0.00759844	synonymous-codon	RNF213	GRCh38.p7	17:80313086	GACCCTTGCTGCTAC[G/T]AAAAGGTGGCTCCGA	57674
rs577176863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80290339	CGTGTGTGTGCGCAC[A/G]TGTGTGCGTGTGCAT	57674
rs577186949	snp	A/G	0.00016503	0.00908228	synonymous-codon	RNF213	GRCh38.p7	17:80345472	TGAGAGGCTCTGCCT[A/G]ACCTTAGGGATCCCC	57674
rs577192942	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80280082	GCCTTCAAGGCAGGC[A/C]TGCTCTTTCCTCTGT	57674
rs577213671	snp	A/G	0.00279162	0.0372561	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391332	CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTTAGT	57674
rs577218209	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381086	TAGCTGCCATCTATG[C/T]GTTTTGGAGATAATT	57674
rs577223154	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80306007	CTTTATTTTATTTTT[C/T]AAAGTAGAGACAGGG	57674
rs577223820	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80340456	GCAGGTGGAGAAACC[A/G]AGGCTCAGGGAGGGT	57674
rs577243499	snp	G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80264452	TTTTGTTGGCTTCTG[G/T]GGCCTCAGACTGGTT	57674
rs577257149	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292898	CTGCCCCCTGGTGTC[C/T]GGTGTCTTGGAAACA	57674
rs577278877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381419	ACCTGGATCACTCCG[C/T]CGTTTTCATCTTAGA	57674
rs577289660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80288984	ACCCAGGTGGGCCCC[A/G]AGGTACCATGGCACC	57674
rs577311010	snp	A/G	0.000862677	0.0207508	intron-variant	RNF213	GRCh38.p7	17:80340387	GGGTGGGCAGGCCCC[A/G]TCTCCCAGGGACTGC	57674
rs577320102	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355672	GGAATGGGGGCTTAC[-/A]GGGGGAAGAAGCGGG	57674
rs577321939	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395351	TCTATTTATGGCACA[C/T]AGACATCAGCTAGGC	57674
rs577322348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369364	GATCGCGCCACTGTA[C/T]TCCAGCCTGGGCAAC	57674
rs577323237	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320480	GCCTCAGCCTCCCAA[A/G]TGCTGGAATTACAGC	57674
rs577326759	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80350535	TTCCCCCGCCTCATT[C/G]CCCCAAGTGGGATTA	57674
rs577401417	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80270730	TTGTTGGGACTGTTT[A/G]TACTGGGAACAGCCT	57674
rs577450681	in-del	-/C	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381495	TACCAGGCTCACCAT[-/C]TTCTCTACAAACCAG	57674
rs577454769	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385979	CCAGCACTGTTAACG[C/T]TTAACTTGTGTCTCT	57674
rs577462525	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80270300	GCTGTTTTGCCGTGA[C/G]ATAGGCTGCTAGGCT	57674
rs577488507	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320810	TAAGACCCTGTCTCT[A/T]TAAAAACTAAAAAAT	57674
rs577488817	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385496	TTGGCCCTTTCAGGG[C/G]GTTGCTATCATACGG	57674
rs577491071	in-del	-/TGG	0.0901694	0.192235	intron-variant	RNF213	GRCh38.p7	17:80313633	TTGTGGTGGAGGTGA[-/TGG]TGGTGATGGTGATGG	57674
rs577502459	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80285044	CCAAGGGACCATTCC[C/G]CAGGATGGGCCATCC	57674
rs577506214	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355113	CCCCAGACAGAGGGT[A/C]TCTTTAAGACAGACT	57674
rs577531725	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80262686	TGAATAGCCATCTCA[A/G]AATTGACCACAGAAT	57674
rs577547581	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80298950	TGCTACTGCACTGTA[A/G]CTTGGGCGACAGAGC	57674
rs577571387	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80349985	TGGCGATGGTACCCG[C/T]GCCGGTTAATGAGCG	57674
rs577630509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364285	GGGGGCGGGCCAGGA[A/G]GTATGTCACATAGGG	57674
rs577639463	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376002	TTCTCAACCTTGTTA[C/T]GTGGAGGAACACATA	57674
rs577644855	snp	A/G	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358345	GCTGGCGAGCATGAT[A/G]TCATTCATCGACAGA	57674
rs577662080	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320212	CTCCCCTCTGCAGGC[A/T]TAAACAATTGCTGAA	57674
rs577663484	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF213	GRCh38.p7	17:80278103	TGCTGGGTTGTACTT[-/C]CTGTGGTGAGGGAAG	57674
rs577669540	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353874	TTGGGGGGTGCAGGG[C/T]GGAGGTCGGCGTCTC	57674
rs577672022	snp	A/C	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80263227	GGCTGCCTGCTCAGG[A/C]CCCATCACCTGTGGG	57674
rs577690513	in-del	-/AGGATGTTC	0.00169575	0.0290689	splice-acceptor-variant	RNF213	GRCh38.p7	17:80307126	TTTTTTCTCTGCCTT[-/AGGATGTTC]AGGATGTTCAGAACG	57674
rs577698176	snp	A/G	1.64904e-05	0.00287139	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386723	CGAGGTCACTGAACT[A/G]CATGTCATCAGTTAT	57674
rs577698467	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80326218	AAGCGCTGACCTCCC[A/G]GGCTCACGTGATCCT	57674
rs577718546	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356389	CTTCCCCACTCTGCT[C/G]TTCACGCAGCACTAG	57674
rs577724331	snp	A/G	0.00159617	0.0282053	intron-variant	RNF213	GRCh38.p7	17:80338662	TTAAAAAAAAAAGAT[A/G]ATTTAAAAAAATTAA	57674
rs577752066	snp	C/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80278062	CCTTTGTGCATTCTT[C/T]CTCTGGAGAGGCTAC	57674
rs577770919	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378203	CCACTGCAGCATGGG[A/G]TCAGTGAGCCTTGTC	57674
rs577782533	snp	A/C	0.00438332	0.0466095	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261081	CCCGGTCCAGCCCCG[A/C]CCGCGGCGCCCACTG	57674
rs577788425	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80337258	TGGCAGAATGATGGC[A/G]TCTGGTAGAGAGGCA	57674
rs577788889	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80330369	GGGTTGGCCCTCTGC[A/G]GGGTGCTGCCGTGGG	57674
rs577824270	snp	A/G	0.000314311	0.0125322	intron-variant	RNF213	GRCh38.p7	17:80298273	GACTCCCAGGGAGAT[A/G]ACTCCCTGGCCAGCT	57674
rs577828033	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80336919	AAAAAGAAAAGAAAA[C/G]AAAAAAGTAAACATT	57674
rs577843819	snp	A/G	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80269438	CCATTCATCTATTCT[A/G]TCTATCCATCCATCT	57674
rs577874494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380060	TATGTCTGCAGGACC[A/G]AAACCTGGGCATCCG	57674
rs577887273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303878	TGTGCCTGGCCAGCC[A/G]TTGGGAACCAATTCT	57674
rs577887784	in-del	-/AG	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360841	CCATTTGGAAGACTC[-/AG]GGTGGCCTTCTTTTC	57674
rs577907317	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80344603	TCCAATATAGATAAC[A/G/T]TGGAGGGTTAAGACA	57674
rs577917506	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80325406	TAACAGCCACTATTC[A/G]TTGAATGCTTGCTGT	57674
rs577959340	in-del	-/CGTGTA	0.0023933	0.0345097	intron-variant	RNF213	GRCh38.p7	17:80290390	GCGTGCACGTGTGTG[-/CGTGTA]CGTGTGCTTGTGTGT	57674
rs577969188	snp	G/T	0.000798403	0.0199641	intron-variant	RNF213	GRCh38.p7	17:80282874	GGCTAATTTTTGTAT[G/T]TTTAGTAGAGATGGG	57674
rs577975389	snp	A/C/T	0.00103853	0.0227643	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288020	CAGGCACAGCCACCA[A/C/T]GCCACTGGAGGGTGA	57674
rs577982374	snp	A/G	6.68729e-05	0.00578204	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363627	CTGGACGCATTTGCC[A/G]CAATGGCCTGCACGG	57674
rs578002904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80309617	TTGTAGCTTGAATAC[A/G]GTAACAAAGGCCATA	57674
rs578049901	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319771	CGGCAAAGGGGAAGA[G/T]ATTGTGCCCCCCTGT	57674
rs578075706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80292283	GAGACAGGGTTTCAC[C/T]ATGTTGGACCTTGAC	57674
rs578098530	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394250	CTGACATTTTGAAAT[C/T]GTGAGAGAAACTAGA	57674
rs578127173	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80286789	AGTCACTTTCCTGTA[C/G]TGACCTGATCCACAC	57674
rs578143578	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80303101	TACTCAAGGCACAGC[A/G]TGTACAGCACTGCTC	57674
rs578172846	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80303787	GTTGGCCAGGCTGGT[C/G]TTGAACTCCTGGCCT	57674
rs578191065	snp	C/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80261510	GAGTCCAGGGCGGGA[C/G]GGGAAGGAGCTGTGC	57674
rs578193532	snp	A/T	0.00199481	0.0315187	intron-variant	RNF213	GRCh38.p7	17:80324873	AAAATTTTCGAAGAA[A/T]TGTAAAGTGTTTTAC	57674
rs578201145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367658	ACACGGCGCAGCCTT[A/G]GCCCTGAATGTGGTG	57674
rs578205638	snp	C/T	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80297703	GAGGCAGGAGAATGG[C/T]GTGAACCCGAGAGGC	57674
rs578234501	snp	C/T	7.47203e-05	0.00611184	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373180	GGTGAGAAGCGGGGC[C/T]GGGCAGCACACAAAC	57674
rs578235859	snp	A/G	0.00438332	0.0466095	intron-variant	RNF213	GRCh38.p7	17:80297248	CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	57674
rs578242212	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80291913	GTCTCTCTGGAGAGC[A/G]CAGACTTTGCCTGGG	57674
rs578245203	snp	A/G	0.000399281	0.0141238	intron-variant	RNF213	GRCh38.p7	17:80329341	CTAGAATTACAGACC[A/G]GAAGTCATTTTCCTT	57674
rs578250374	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393623	TGTCAGCGTAGCACC[A/G]AATTCAAGACCAAGG	57674
rs745312811	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80337826	TTCTAACCTATGCTC[C/T]TCACAGATTTCCCCA	57674
rs745315304	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392775	TTGTATTTTTACTAG[A/C]GACAGGGTTTCTCCA	57674
rs745332162	snp	C/T	1.85098e-05	0.00304213	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385669	TCCAGGAGAGCCTCG[C/T]CTGAAAGCTCTTCTC	57674
rs745332899	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80293065	TAAACATATATATAT[-/A]TTTTTTTTCTGAGAC	57674
rs745342704	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296041	TTGTTTTCCCCCCAG[A/G]CGGCGTCTCACTCTG	57674
rs745346612	snp	C/T	0.000115614	0.0076022	synonymous-codon	RNF213	GRCh38.p7	17:80332091	AGTGAGACTGTCCAC[C/T]TCCTCGAACTCGCAG	57674
rs745351816	in-del	-/CTGGCCAAGATGCTGAAACCCCTGTCTCTACTAAAAACA	1.69618e-05	0.00291215	intron-variant	RNF213	GRCh38.p7	17:80273430	GCCTCGGCTCCCCTC[lengthTooLong]CGCCCCCGCTCACTC	57674
rs745353314	snp	A/G	1.64972e-05	0.00287199	missense	RNF213	GRCh38.p7	17:80346403	TTGATGCTGGCCATC[A/G]GGGTGTGTTACCATG	57674
rs745357663	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80269327	CACCTGATATTAACC[A/G]TCACACCGTCTATCC	57674
rs745360387	snp	C/T	8.28233e-05	0.00643465	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354586	ATTCAGGTACTGTGA[C/T]TAAAGGAAGCAAGGA	57674
rs745364464	snp	A/T	3.29783e-05	0.00406055	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351738	ATGAGGACCGTATCT[A/T]CGTCTATTTCATCAC	57674
rs745370129	snp	A/G	3.29495e-05	0.00405877	missense	RNF213	GRCh38.p7	17:80345347	ATCAGTCACTTGACT[A/G]GGAAGGTCATCAAGA	57674
rs745392081	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312719	GGGCACAGCCTGGGG[A/G]CCTGCTCATTGGCAG	57674
rs745409613	snp	G/T	1.69146e-05	0.0029081	intron-variant	RNF213	GRCh38.p7	17:80295858	TATAGCTATTATAAT[G/T]ATTTTCTCTGATTGC	57674
rs745415242	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337208	CAGCCATTGCTTCCA[A/G]CGTCACCCCCAGAGG	57674
rs745419537	snp	A/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354498	TAAAGAAGCAAGAAG[A/T]GAGCCAGTTTCACCC	57674
rs745421847	snp	A/G	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80290671	TCTTCATCAGAGGAG[A/G]AGAAGAATTTGGGGA	57674
rs745443824	snp	A/G	3.29468e-05	0.00405861	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367993	GCTCCATCTGCCTGG[A/G]AGATGCAAAGGACCC	57674
rs745450416	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351827	AGAACATCAGTCAGG[A/G]TATTTATTTATGTAT	57674
rs745451198	snp	A/G/T	3.30252e-05	0.00406346	synonymous-codon	RNF213	GRCh38.p7	17:80347914	GGAGGAGCTCTGTGC[A/G/T]TGGGTGGAGAAGTTC	57674
rs745461203	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80268846	GCTCACACAATCACA[A/C]GGTGAAGTCCCATGG	57674
rs745477582	snp	C/T	1.65168e-05	0.00287369	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369458	TCTGTAAGGAGGCAT[C/T]TGGGAAACACCATCC	57674
rs745484496	in-del	-/CACCTCTTAGCATGTAGGTCACACGGCGTGGA	1.65031e-05	0.00287251	frameshift-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352995	ACCCTCATGGTTTCT[lengthTooLong]GATGTGACCAGGCTG	57674
rs745502967	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372366	TAAAATAAAAAGGAA[C/T]GTTAGGTTTCCATAA	57674
rs745504131	snp	C/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80306371	TGTATATGGAAAACT[C/T]CATTGAGCACCTGGG	57674
rs745514409	snp	A/G	1.64825e-05	0.00287071	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368089	AGATGATATGCCCCT[A/G]CTGTTTAACTGCCTT	57674
rs745514604	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349115	GGATGGGGGGTGGAG[A/G]GGTCCGGGGCGACCC	57674
rs745516474	snp	A/G	0.000116381	0.00762737	synonymous-codon	RNF213	GRCh38.p7	17:80332340	TCAGCCTTCTTACAG[A/G]AAGTTCATTAAGTTG	57674
rs745531099	snp	A/G	1.69545e-05	0.00291152	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376951	AAGGGTCTGGAGCGA[A/G]TCCACTGGTACAGTA	57674
rs745536230	snp	A/G	2.20714e-05	0.00332193	intron-variant	RNF213	GRCh38.p7	17:80317141	ATGGGAGTGTGCCGT[A/G]GCATTTAGTCGTGAG	57674
rs745541663	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80315093	GTGATGGTGGAGGTA[A/C]TGGAGGTGATGGTGG	57674
rs745547008	snp	A/G	1.65059e-05	0.00287275	missense	RNF213	GRCh38.p7	17:80345482	TGCCTGACCTTAGGG[A/G]TCCCCCAGGCCACCG	57674
rs745548240	snp	A/G	1.65457e-05	0.00287621	intron-variant	RNF213	GRCh38.p7	17:80290750	GTGTCTGTAGGCTTG[A/G]GAGGAATCCCTCAGG	57674
rs745555250	snp	C/T	0.000118828	0.00770714	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376595	AACACCCCCCAGAGC[C/T]TGTCACTGTAGAGAC	57674
rs745558850	snp	A/G	1.86197e-05	0.00305115	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381728	AGCTCTCTAGCAGAA[A/G]TGAGGAAAGGGGCAA	57674
rs745568630	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384033	ATTCTTAACAGACTA[C/T]TCCAGTGCTTTGGTT	57674
rs745575441	snp	A/C/G	3.32145e-05	0.00407509	missense	RNF213	GRCh38.p7	17:80347990	CCCTCTGACGTCTTC[A/C/G]TCGGCTACCACTCGG	57674
rs745578798	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80300053	TTTATAATAGAACGA[-/T]TTTATATTGTTTTTG	57674
rs745580000	snp	C/T	3.29794e-05	0.00406061	stop-lost, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393496	AATCGAGAAATGAGA[C/T]AGAATTATTTCCTCA	57674
rs745586717	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390059	AGCGGATCTGAGCCC[A/G]GAAAATGCTAAGCTC	57674
rs745614266	snp	A/G	1.75786e-05	0.00296462	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386854	AGCGGCAGATCGTCA[A/G]CCGCTTCCTCCAGGG	57674
rs745637389	snp	C/G	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383865	AGTTGAGTACCTCCA[C/G]CACATTGTGGAACAG	57674
rs745640905	in-del	-/GTGCATGC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379050	CATGGTGGTGCATGC[-/GTGCATGC]GTGCATGCGTGCATG	57674
rs745642649	in-del	-/C	0.000266733	0.0115454	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358240	GGTGGCAGACCGCCA[-/C]TCTGGTTCCTCTGAC	57674
rs745648896	snp	C/T	6.62712e-05	0.00575597	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360112	CCACATGAACCTTTC[C/T]GAGAACGCTTCCAAC	57674
rs745653997	snp	C/T	1.66305e-05	0.00288357	intron-variant	RNF213	GRCh38.p7	17:80273233	CCTTCCTTCATCTGC[C/T]GTTACAGATTCTGAG	57674
rs745666956	snp	A/G	0.000379566	0.0137709	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368138	AGCTGTTTCCCAAGC[A/G]CACAGGTACAACACC	57674
rs745667885	snp	A/G	3.37177e-05	0.00410582	missense	RNF213	GRCh38.p7	17:80346964	GATCCCGCCCCCCAC[A/G]AAAAGGTCGGCTTCG	57674
rs745674598	snp	C/G	1.6492e-05	0.00287154	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390117	CTAGACGCCTTCCTG[C/G]TAGAGCTGCACGAAA	57674
rs745676999	snp	A/G	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80343920	TACTTAATGGATATA[A/G]ATGGGAAAATGTGGC	57674
rs745692862	snp	C/T	1.65094e-05	0.00287305	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386801	CCAGGTGGAGGAGGG[C/T]AGAGAGACCGTGCAG	57674
rs745694603	snp	A/G	3.29544e-05	0.00405908	missense	RNF213	GRCh38.p7	17:80345561	TTGCCATCGAGATGC[A/G]GTTCCGGTGTGGGAT	57674
rs745716843	snp	G/T	1.69533e-05	0.00291142	intron-variant	RNF213	GRCh38.p7	17:80263818	GGCTGGGGCAGTGGG[G/T]ACCCCTGGAGATGTC	57674
rs745717325	in-del	-/CCT			intron-variant	RNF213	GRCh38.p7	17:80322160	CCCCCCCACCCCCCC[-/CCT]TTTTTTTTTTTTTTT	57674
rs745722686	snp	A/G	1.68721e-05	0.00290444	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353992	GTCAGTGGCAGAAAC[A/G]GATGACCCAACCGTC	57674
rs745748901	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80262324	AAGGGATGCAAATTG[A/T]CCCATACACCTATTG	57674
rs745755036	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367488	AAGTTTGAAATATCT[C/T]AGTGAGAGCGGAGGA	57674
rs745765799	snp	C/T	1.66139e-05	0.00288213	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319515	TGTGCTGCACAGTCC[C/T]TGCTGCTCGCACCAT	57674
rs745772171	in-del	-/CAAAA			intron-variant	RNF213	GRCh38.p7	17:80277055	AGCGAGACTCACTCT[-/CAAAA]CAAAGCAAACAAACC	57674
rs745781266	snp	C/G/T	3.3116e-05	0.00406904	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371986	ATCAACTGCCTGGAG[C/G/T]TAAGTGAACTCTCTC	57674
rs745809057	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80329742	AGGCTGAGGCAGGAG[G/T]ATCACTTGAGCCTGG	57674
rs745815251	snp	G/T	0.000396242	0.01407	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385058	CAGAGCTGAGGCTGG[G/T]AAAGTTCCTGCCTGA	57674
rs745823468	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299930	AGTATTCCATGGTGT[A/G]TATGTACCACATTTT	57674
rs745824744	snp	C/T	2.23008e-05	0.00333914	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374634	ACCAGGTGGCATCCC[C/T]TGGAGCCTGCATGTT	57674
rs745834222	snp	G/T	2.80911e-05	0.00374763	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371861	ACCAGGAATAATATT[G/T]CTCTTTCTGCAGCTT	57674
rs745838852	snp	A/C			intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261409	GTCCTTCCGACTTGG[A/C]GAAGTCGCCCGAGCG	57674
rs745839370	snp	C/T	1.65707e-05	0.00287838	synonymous-codon	RNF213	GRCh38.p7	17:80347074	AGAGCTCATAGAGAG[C/T]GCCAAGGGCATCTGC	57674
rs745848105	snp	C/T	1.64917e-05	0.00287151	stop-gained	RNF213	GRCh38.p7	17:80294968	TATGAAGGACAGGCA[C/T]AGCTGTGGACCGATT	57674
rs745851224	snp	A/C	1.64798e-05	0.00287047	synonymous-codon	RNF213	GRCh38.p7	17:80346034	AGGCAGCTGGTATAC[A/C]GGGTCCATGCTCTGC	57674
rs745851562	snp	C/G			missense	RNF213	GRCh38.p7	17:80327938	ATTTTAGTTGGACAA[C/G]TGGAGCTGATTATAA	57674
rs745871283	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300692	CTGGGTAGCTGGGAC[C/T]ACAGGCACCCCACCA	57674
rs745879321	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341004	GAGATGTGGCTTCAC[C/T]GTGTTAGCCAGGATG	57674
rs745883063	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352763	GAATCGGGTCGTGTA[C/T]AGTATCGGGTTGGGT	57674
rs745888300	snp	C/T	1.64841e-05	0.00287085	intron-variant	RNF213	GRCh38.p7	17:80309202	ACACAAGGTATCACA[C/T]CCGGGATAGGTGCGG	57674
rs745889964	snp	A/G	6.58892e-05	0.00573936	missense	RNF213	GRCh38.p7	17:80345169	CCCGGGGAAGCACAT[A/G]GTCACCATGGATGGG	57674
rs745896294	snp	C/G/T			intron-variant	RNF213	GRCh38.p7	17:80298719	CCTGTAATCCCAGCA[C/G/T]TTTGGGAGGCTGAGA	57674
rs745912051	snp	C/T	5.01819e-05	0.00500884	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288001	GGCCAGCCGAGCCAG[C/T]CCCCAGGCACAGCCA	57674
rs745926097	in-del	-/TTAGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382846	ACTACTTCAAAATAC[-/TTAGA]TTAATTTAGAAAGCT	57674
rs745926738	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80271256	GTGATGTTTCATGTG[C/T]GTCTTATGTATGTAG	57674
rs745927464	snp	A/C/G	5.07896e-05	0.00503911	synonymous-codon	RNF213	GRCh38.p7	17:80350301	TCCCTTTTCTTTCAG[A/C/G]AACTGTTTAACGAAT	57674
rs745937199	in-del	-/CT	1.64727e-05	0.00286986	frameshift-variant	RNF213	GRCh38.p7	17:80306338	GGTTTAGTCTGCTAC[-/CT]CTGAGTCACCTGGTT	57674
rs745942407	snp	C/T	1.64876e-05	0.00287116	missense	RNF213	GRCh38.p7	17:80347549	GAGATTATTTTTGGT[C/T]CTGGTTTCCCCAAGG	57674
rs745952693	snp	A/G	1.65018e-05	0.00287239	missense	RNF213	GRCh38.p7	17:80349906	TCCTCAAAGAAGTCC[A/G]GTGAGGTTCCCTGCC	57674
rs745974784	snp	C/G	1.64765e-05	0.00287019	missense	RNF213	GRCh38.p7	17:80346117	TGAAAAGCTCTACAT[C/G]CAGCAGATTGTCCAG	57674
rs745976705	snp	A/G	3.29462e-05	0.00405857	missense	RNF213	GRCh38.p7	17:80345059	CCGAGTTTTATTGGC[A/G]ACACACTGAGGGGCT	57674
rs745980397	snp	C/T	1.66219e-05	0.00288283	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354104	AGAACGAGAGCTGCA[C/T]GCGCAATATGCGGAG	57674
rs745985036	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325772	AGTTGGCGTGTGAGA[C/T]CTTAGATTCATATCT	57674
rs746002215	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283457	GGGTCTCTCCTGCAG[C/T]TGCGTCTGCGCTTAC	57674
rs746003961	snp	C/T	1.66632e-05	0.0028864	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287902	CTTTCTCCTGCCAGC[C/T]CCTGTCACCTGACTT	57674
rs746010665	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80349922	GTGAGGTTCCCTGCC[A/T]TCCCTGCTGCCCTCT	57674
rs746014661	snp	A/C	5.1917e-05	0.00509469	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386898	AGCCTCAAGGTAGGG[A/C]TGACTCCTGCCACTG	57674
rs746023023	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259337	GCCAGGCTTGGTGGC[A/G]GGCGCTTGTAATCCC	57674
rs746034668	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80324912	TCTTTTTGTGGCCTT[-/A]TAAAACAAGTTACAG	57674
rs746055990	in-del	-/T	2.09888e-05	0.00323944	intron-variant	RNF213	GRCh38.p7	17:80317301	AGTTTGGGGGCAGTC[-/T]TTTCAGGGCGTGAAG	57674
rs746059836	snp	C/T	1.65583e-05	0.00287731	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358273	GTGGTGGCCCATCTC[C/T]CTTCTGTGCTGCAGG	57674
rs746082394	snp	C/T	0.00022831	0.0106819	synonymous-codon	RNF213	GRCh38.p7	17:80334206	CAGCGAGGCCCGGTG[C/T]AAGGGGCTGCAGGCT	57674
rs746110139	snp	C/T	3.29457e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376398	TGGACAATTCTGTGC[C/T]ATTGTTGAGGGCGGG	57674
rs746112449	snp	A/C			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395834	GTGGTCTAGAACCAC[A/C]GCAAGAAGAGGAGGC	57674
rs746137859	snp	C/G	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389838	TGCAGGCCTTAAACA[C/G]ATGCCAGTTAAAACA	57674
rs746145556	snp	A/G/T	8.23993e-05	0.00641823	missense	RNF213	GRCh38.p7	17:80347678	GAGAGCCTCTACGAC[A/G/T]CACTCAACCAGTACT	57674
rs746168739	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360812	AATAGTCTTTTCCAC[A/G]TTTACTTATCGTACC	57674
rs746177359	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80334369	AATACCTCCCCTTGG[C/G]CAAGGACTACGTAAA	57674
rs746182028	snp	C/T	0.00011458	0.00756816	missense	RNF213	GRCh38.p7	17:80336367	AAGGACCAGTACCTG[C/T]CCAGGAAACTGGTGA	57674
rs746188573	snp	A/G/T	5.31979e-05	0.00515719	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383116	TCCTCGGTCCAGAAA[A/G/T]GAAGGGTCCCGGCGT	57674
rs746195087	snp	A/G	1.64909e-05	0.00287144	intron-variant	RNF213	GRCh38.p7	17:80319163	GCATCCGAAAGCTCT[A/G]AAACCACCCCCCTTT	57674
rs746203743	snp	C/G/T			intron-variant	RNF213	GRCh38.p7	17:80292209	CCTGTCTCAGCCTCC[C/G/T]GAGTAGCTGGGATTA	57674
rs746210237	snp	A/G	3.35323e-05	0.00409451	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390220	TTGCACACCTATGGG[A/G]CGGGGCAGACACAAT	57674
rs746217439	snp	C/T	1.67447e-05	0.00289345	synonymous-codon	RNF213	GRCh38.p7	17:80346687	GACCATCGTGGCAGA[C/T]GCCATGCAGGGCCCG	57674
rs746239882	snp	C/T	1.64961e-05	0.00287189	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386415	CCGTGGAAAAACTCT[C/T]CAAGGAAAACAACAG	57674
rs746241076	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382772	TTATGTAGGATAGAG[C/G]AATTTTTAGAGATTG	57674
rs746242138	snp	A/G	1.66502e-05	0.00288527	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383044	TGGGAAAAGGAAATC[A/G]CAGCTGTGATTTCTC	57674
rs746266490	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80297907	GGTTATAATGATCGC[A/C]CCACCGCGCTGCCTT	57674
rs746279111	snp	A/G	0.0001154	0.00759518	missense	RNF213	GRCh38.p7	17:80346346	CTCTCCAAGTCCAGC[A/G]TCAGCAAAAATCACA	57674
rs746280089	snp	A/G	1.6476e-05	0.00287014	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369572	GACCTGGTGTCCACC[A/G]TTTGCTTCAAGGACA	57674
rs746290208	snp	A/G	1.70243e-05	0.00291751	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373145	CAGTGGGTGTTTCCC[A/G]AGGACGTTGTCAAGC	57674
rs746294783	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80264961	CTCCTTCCCCTCTTT[A/C]AGTCTTTGCCCAGCT	57674
rs746304969	snp	C/G	1.66496e-05	0.00288522	missense	RNF213	GRCh38.p7	17:80273328	AGGAAGGGGGCCCGT[C/G]CTTGTTCCCGGGCTC	57674
rs746310220	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80276537	GAACAAGAGAAAACC[G/T]ACATGAACAAGAGAA	57674
rs746314463	snp	A/G	3.303e-05	0.00406373	missense	RNF213	GRCh38.p7	17:80348170	TCGCTGGGCGGGTTC[A/G]CAGCGGAGTGGCTGT	57674
rs746323542	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80276375	AAAGTGCTGGGATTA[C/T]GGGCGTGAGCCACCA	57674
rs746330372	snp	C/T	1.648e-05	0.0028705	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288773	GCGTCTCCTTCCTGC[C/T]TGCCGGCTCCAGGAG	57674
rs746331109	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382088	TTCCCCTACCATGCT[A/G]GGAGCACGTGTCGTC	57674
rs746340637	snp	A/G	1.64849e-05	0.00287092	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364411	GCCGAGTGAGTGAGT[A/G]AGTGGCGCCCTCTTT	57674
rs746342023	in-del	-/C	2.57056e-05	0.00358499	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372939	AAATGCCCTAAGTCA[-/C]CCAGCCACTCACCCG	57674
rs746386871	snp	A/G	9.53607e-05	0.00690444	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363802	TCAGGTGAGACCCAG[A/G]AGCCCTCACCCACTG	57674
rs746393466	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	RNF213	GRCh38.p7	17:80319276	GGCCAAGACCTTCGA[A/G]AAATGCATCATTGAA	57674
rs746394718	snp	C/T	1.64762e-05	0.00287016	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288620	CTTGGCTCTGGTGTT[C/T]GGGGTCTTTCAGGCA	57674
rs746406516	snp	C/T	1.67531e-05	0.00289418	intron-variant	RNF213	GRCh38.p7	17:80291855	AGCAGGCTGTCTGCT[C/T]ACCCCTCCGGAGTGC	57674
rs746424283	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	RNF213	GRCh38.p7	17:80345733	CTCCAGAGTCAGGGA[A/G]GCTGAAAATGTGGCC	57674
rs746426920	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390405	GTGTTTTTCAGACAA[A/G]AGTCTTGCCCTGTTA	57674
rs746434670	snp	A/G	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377833	AGGGTTTGAGGGGTG[A/G]CGTGCACTCCTGGGT	57674
rs746441238	snp	A/G	1.64906e-05	0.00287142	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393383	ACATGCAAACTAAAG[A/G]AAGTGAAATTCTTCC	57674
rs746443738	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328534	GGGTTAGAGGAGAAC[A/G]CAGTAAGAATGGATC	57674
rs746455328	in-del	-/ACTAGAG			intron-variant	RNF213	GRCh38.p7	17:80314158	GGTGATGGTGGTGGT[-/ACTAGAG]GTAGGTGATGGTGGA	57674
rs746455713	snp	C/G	1.67843e-05	0.00289687	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382980	GAGTTTTTTTGTAGG[C/G]CTTTTAAATTTTGAC	57674
rs746466394	snp	A/G	6.60066e-05	0.00574447	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390125	CTTCCTGCTAGAGCT[A/G]CACGAAATGATAATC	57674
rs746467687	snp	C/T	3.29527e-05	0.00405898	missense	RNF213	GRCh38.p7	17:80345566	ATCGAGATGCGGTTC[C/T]GGTGTGGGATCCCGG	57674
rs746475303	snp	A/G	1.80788e-05	0.0030065	missense	RNF213	GRCh38.p7	17:80317228	AATTCCCCGCGGAGC[A/G]TGGCTGGAAGGAGTC	57674
rs746489967	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374697	GACCACTGATGCAGC[C/T]CATCACGTGACACTG	57674
rs746496977	snp	A/C/T	6.59994e-05	0.00574421	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352962	GCAGTCTGTCCACAT[A/C/T]GATGACCTCCGGAGA	57674
rs746515955	snp	A/G	1.6546e-05	0.00287624	missense	RNF213	GRCh38.p7	17:80348008	GGCTACCACTCGGAC[A/G]CCTGCGCGTCTGTGG	57674
rs746522809	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389723	AGTACAGGGCAGAAC[A/G]AAGAGAAGAATGCCT	57674
rs746534578	in-del	-/T	1.66877e-05	0.00288852	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358497	GAGTGGAAGGCTTTC[-/T]TTCCCTGGGGAGAGA	57674
rs746536509	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353158	AGGAGCAGGGCCACC[A/G]TGTTTCGTCCCTCGG	57674
rs746549519	snp	C/T	0.000308785	0.0124216	intron-variant	RNF213	GRCh38.p7	17:80339180	GCTCTGTGAGCCAAC[C/T]TCATGGTTCTGCCTC	57674
rs746558151	snp	C/T	1.65111e-05	0.0028732	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369473	TTGGGAAACACCATC[C/T]ACCTGTCTTCTGTTT	57674
rs746559042	snp	C/G			missense	RNF213	GRCh38.p7	17:80327869	GCCAAGAGGCTGATA[C/G]CTGTTGCCGACTCTG	57674
rs746580184	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80285621	TGATGACGCCACTCT[A/G]CAGTGCTGGGCCCCA	57674
rs746581969	snp	G/T	1.9201e-05	0.00309841	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351843	TATTTATTTATGTAT[G/T]TATTTATTTATTTGT	57674
rs746590204	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296891	TTCACCATGTTGCCA[C/T]GGTGGTCTTGAGCTC	57674
rs746601234	in-del	-/TCT	1.65206e-05	0.00287403	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367750	TGCCTTTCTTCAGTG[-/TCT]TCGAGAGAACTCTGA	57674
rs746622661	snp	A/G	1.73264e-05	0.00294328	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363771	GGGAGCCTGGCCCAG[A/G]CTGTCATCAGGGAAG	57674
rs746644345	snp	C/T	3.29886e-05	0.00406118	intron-variant	RNF213	GRCh38.p7	17:80319146	TAGAGCACTGGAGCG[C/T]TGCATCCGAAAGCTC	57674
rs746646243	snp	C/T	1.69525e-05	0.00291135	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363734	GGAGCTCATCTGCTC[C/T]GATGAGCACATGCAA	57674
rs746646987	snp	C/T	2.56947e-05	0.00358423	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374646	CCCTTGGAGCCTGCA[C/T]GTTCCCTGGTTTATG	57674
rs746647528	snp	C/T	8.24246e-05	0.00641915	intron-variant	RNF213	GRCh38.p7	17:80307117	TGTTTTTCTTTTTTT[C/T]TCTGCCTTAGGATGT	57674
rs746648001	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296095	CGCAATCTTGGCTCA[C/T]TGCAGCCTCCACCTC	57674
rs746649526	snp	A/G	3.30376e-05	0.0040642	missense	RNF213	GRCh38.p7	17:80294980	GCACAGCTGTGGACC[A/G]ATTTGCAGTACAGGG	57674
rs746653404	snp	A/C	3.29549e-05	0.00405911	intron-variant	RNF213	GRCh38.p7	17:80344656	TTCTTGTAACCATTT[A/C]ATTAATGTCTCTCCT	57674
rs746663563	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338006	TTCAGAGGTGAGGGC[A/G]CATCTTTGCAGTGGC	57674
rs746666759	snp	C/T	1.65015e-05	0.00287237	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374550	TGTGGCCAAAGCTGT[C/T]CTCGAGTGCAAGCCA	57674
rs746668187	snp	C/G	1.65919e-05	0.00288022	missense	RNF213	GRCh38.p7	17:80306454	CCGGGACTTGAGCAA[C/G]TCTTGAATACGCAGG	57674
rs746687526	snp	A/G	0.00015484	0.0087975	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288327	CGGGACAGAACTGCA[A/G]ACCACCGAGCAACAG	57674
rs746688830	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377720	AATGTGGGTCATTGG[A/G]TGAAACCTCATTAGC	57674
rs746695587	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375095	TTTTGAGTCCCTGTG[C/T]CAGGAAAAGAGGAAA	57674
rs746707430	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357831	AAATAAAATAAAATT[G/T]AAAAATTAGCTGGGC	57674
rs746712700	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385809	TCACTGCAACCTCTG[C/T]CTCCCGGATTCAAGC	57674
rs746714191	snp	C/T	1.79239e-05	0.0029936	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386860	AGATCGTCAGCCGCT[C/T]CCTCCAGGGCAAGCC	57674
rs746722534	in-del	-/GAGGTGGCA	9.92228e-05	0.00704284	cds-indel, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353580	GCCAGCACATCAGGG[-/GAGGTGGCA]GAGGTGGCAGAGGAG	57674
rs746730141	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80309565	TTTCCTCCCAAAAAA[A/T]ACATGTCCAAACATG	57674
rs746731021	snp	C/T	1.6669e-05	0.00288691	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390186	GAGGAGCGCTTCCGC[C/T]CTCAGTGGAGGTATG	57674
rs746750997	snp	A/C	1.64735e-05	0.00286993	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385098	CTTGCAAAGGGATCT[A/C]GTGAAGCAGTTCCAG	57674
rs746775894	snp	A/G	0.000120533	0.00776221	missense	RNF213	GRCh38.p7	17:80339849	AGAGGTCTGCAGGTC[A/G]GCCAGCCCAACCTCG	57674
rs746779377	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268913	AGTTGCTCAGTCTGA[A/G]TCCAAAAGCCTCAAA	57674
rs746785852	in-del	-/CGG			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260517	CCTGCGCGGGGCCGG[-/CGG]CGGCGGCGGCGGGCA	57674
rs746803814	snp	C/G	1.65636e-05	0.00287776	missense	RNF213	GRCh38.p7	17:80347102	TGCTCCTCAGACATC[C/G]TCGTCCAGGACCGAG	57674
rs746803857	snp	C/T	3.31422e-05	0.00407063	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383976	TTCGGTGCAGAGTTC[C/T]CCAGCAGGCCTGAAG	57674
rs746806479	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	RNF213	GRCh38.p7	17:80346144	CCAGAGACTGGTTGA[A/G]TCCATCAGCCTAGAT	57674
rs746831806	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80349179	TCATCATGACAGATA[C/G]CGCAGGAACGGACAG	57674
rs746833840	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359869	CTGTGAAACAAAGAT[G/T]GCATAAGACAGTTCC	57674
rs746840755	snp	C/T			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321522	CCTGGGTGTATACCT[C/T]GATGTAGAATTGCTG	57674
rs746843896	snp	A/G	1.67747e-05	0.00289605	intron-variant	RNF213	GRCh38.p7	17:80295529	TCAAGTCCATGGTTC[A/G]TGCATCTTCCTCTTC	57674
rs746880231	snp	C/G/T	8.30056e-05	0.00644183	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371998	GAGGTAAGTGAACTC[C/G/T]CTCTTCCCTGAATTT	57674
rs746888230	snp	A/G	3.32923e-05	0.00407983	missense	RNF213	GRCh38.p7	17:80273316	AGGAGCTGAAGGAGG[A/G]AGGGGGCCCGTGCTT	57674
rs746893917	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363215	CCAGCGTTTCAGAAG[C/T]CGTCTGCAGAACTTT	57674
rs746895668	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369590	TGCTTCAAGGACAAC[A/G]CTCCGCCTGAGAAGG	57674
rs746898574	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80280290	AGGAGAAGAAGGCTC[A/G]GGCTCAGCAGACAGT	57674
rs746910653	snp	A/C	3.32419e-05	0.00407675	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288005	AGCCGAGCCAGCCCC[A/C]AGGCACAGCCACCAC	57674
rs746918056	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376409	GTGCCATTGTTGAGG[A/G]CGGGGCCTAGTGACA	57674
rs746926433	snp	A/T	1.75262e-05	0.0029602	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372561	CTTACTCCAGAAATG[A/T]TGAACTGAACCACCT	57674
rs746926676	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80331888	AGAAAGAAATCCTAG[C/G]AGCTGTGTGCTCTTG	57674
rs746949654	snp	A/T	1.64838e-05	0.00287083	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381512	TCTCTACAAACCAGA[A/T]CCCCGCTGAACACTC	57674
rs746949883	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320690	CCACCGCGCCCGGCC[A/G]AGCATAATGTTTTGA	57674
rs746958738	snp	A/G	1.65272e-05	0.0028746	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380980	TGGGAGCGTCCCAGA[A/G]TTCCCAGGTATAACC	57674
rs746958817	snp	A/G	3.29473e-05	0.00405864	missense	RNF213	GRCh38.p7	17:80346211	GCCTCTCAGGGTTTC[A/G]TGAGGAAAACAGAAG	57674
rs746984741	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80290336	TCACGTGTGTGTGCG[C/G]ACGTGTGTGCGTGTG	57674
rs747001217	snp	C/G	3.05013e-05	0.00390509	intron-variant	RNF213	GRCh38.p7	17:80289865	CCGCAGGGGAGCAAA[C/G]GAGACCCTGCCTGAG	57674
rs747005197	snp	A/C/T	6.58896e-05	0.00573943	synonymous-codon	RNF213	GRCh38.p7	17:80345175	GAAGCACATGGTCAC[A/C/T]ATGGATGGGGTTAGG	57674
rs747005473	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80263374	CCTGGAGCATCCCCT[A/G]TCCCCACCCAGCCCA	57674
rs747016412	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80331150	CAGACTTTGAACCCA[G/T]TCTTCCTTATTTCAT	57674
rs747030606	snp	G/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320581	TTTTAGAAGAGACAG[G/T]GTTTCTCCATGTTGG	57674
rs747031786	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368367	CAGACAACAAATTCA[G/T]AGGAACTAAGCCAGA	57674
rs747033589	snp	C/T	0.000268245	0.011578	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373096	GCGGGGGATGGAGTT[C/T]GTGCAGGGCCTCTCC	57674
rs747056355	snp	C/G	1.65075e-05	0.00287289	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376505	AATGAACTCTTGGAG[C/G]CCCTAAAGAATCTGG	57674
rs747063774	in-del	-/C	0.000128891	0.00802676	frameshift-variant	RNF213	GRCh38.p7	17:80339973	TCTGCACCCCGGCAA[-/C]CACCTTTGAGGAGGT	57674
rs747064388	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80348397	AGGGATCCTGCAGGG[A/T]GATGCTGAGACGCTG	57674
rs747073002	snp	C/T	1.65222e-05	0.00287417	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386428	CTCCAAGGAAAACAA[C/T]AGGTTTGTGCACGAG	57674
rs747079249	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80345236	AAGAGGTGGGAGTCG[A/G]AGCCTCACCCATACG	57674
rs747082954	snp	C/T	1.64827e-05	0.00287073	missense	RNF213	GRCh38.p7	17:80347756	CACCGCGTCAAATGT[C/T]GGGTTCACCCCAACT	57674
rs747083719	snp	A/G	1.64792e-05	0.00287042	missense	RNF213	GRCh38.p7	17:80347691	ACGCACTCAACCAGT[A/G]CTACGTCCACCTCGG	57674
rs747090203	in-del	-/GGA	3.30311e-05	0.0040638	cds-indel	RNF213	GRCh38.p7	17:80347920	GCTCTGTGCGTGGGT[-/GGA]GAAGTTCATCAATGT	57674
rs747097271	snp	C/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358370	GACAGAGACGGCAAC[C/G]TAGAGTTACTGACCA	57674
rs747108985	snp	C/T	1.64743e-05	0.00287	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389857	CCAGTTAAAACACAC[C/T]ATTGCCCTCTGGCAG	57674
rs747110950	snp	A/G	1.65233e-05	0.00287426	synonymous-codon	RNF213	GRCh38.p7	17:80343208	TGTGCCTCTGAAAAC[A/G]ATTCGACTGATCGAC	57674
rs747115196	snp	A/T	3.48493e-05	0.00417414	intron-variant	RNF213	GRCh38.p7	17:80350403	CTCAGCTAAGTATGT[A/T]TTTAGTATTTTTCTC	57674
rs747125033	snp	C/T	1.67231e-05	0.00289159	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363322	GTGAGATGGTATGGC[C/T]CTCCTCCGCCTGCCC	57674
rs747125859	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380274	GTGAGTGGGACCTGC[A/G]TGGGGGCCTCACATT	57674
rs747137978	snp	G/T			missense	RNF213	GRCh38.p7	17:80317268	AGACATGGAATGGAG[G/T]CTCACAAAGGTACCA	57674
rs747143745	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300155	TTGAACTAATTTACA[C/T]TCCCACCAACAGTGC	57674
rs747161345	snp	C/T	3.29848e-05	0.00406095	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358462	TCTGAACATTCCTCT[C/T]GTGATGAATAATGAA	57674
rs747177989	snp	A/G	3.3018e-05	0.00406299	utr-variant-5-prime, intron-variant	RNF213	GRCh38.p7	17:80263634	TAGCAGGCTGCCAGC[A/G]ACTCCTGCTCTTGCT	57674
rs747181491	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352788	TTGGGTGGTTTCTGC[A/G]CAGGCCCATTCCAGG	57674
rs747190022	snp	C/T	0.000134603	0.00820265	intron-variant	RNF213	GRCh38.p7	17:80291863	GTCTGCTCACCCCTC[C/T]GGAGTGCAGGTGCCA	57674
rs747191905	snp	A/G	1.64795e-05	0.00287045	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383717	TGAATAATCTCATCA[A/G]CCAAGATAAGCGTAT	57674
rs747211204	snp	A/G	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369647	CTCTTCGTCCAAAAG[A/G]GGCGCTTAAGAGATG	57674
rs747217825	snp	G/T	1.66214e-05	0.00288278	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353083	CGAGGCGGAGCCCCT[G/T]GGGGAGCAGGTGGTG	57674
rs747220213	snp	A/G	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80319295	TGCATCATTGAAGCC[A/G]TGAGCTCAGCCTGCC	57674
rs747220402	snp	A/G	1.64953e-05	0.00287182	missense	RNF213	GRCh38.p7	17:80291792	AGTACGTCAACCGCT[A/G]TCTGTTCATAAAATC	57674
rs747221149	snp	A/G	1.64806e-05	0.00287054	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379576	ATTTGTGCATAAAAT[A/G]GTACTGCTCCAGAAG	57674
rs747225465	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80316673	AGGGCTAGGGTCTTA[A/G]GAGACCCTGCCCAGG	57674
rs747249451	snp	A/T	1.70507e-05	0.00291977	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363581	GGAGGGGCACCGCTC[A/T]GCCACGCCCTGCTGT	57674
rs747253900	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284628	ATTGAGGAAGTTTAT[C/T]ATGGACACACCTGAT	57674
rs747282369	snp	C/T	0.000100653	0.00709339	missense	RNF213	GRCh38.p7	17:80346701	ACGCCATGCAGGGCC[C/T]GGCTGCCTACTCAGA	57674
rs747285701	snp	A/G/T	9.88703e-05	0.00703039	intron-variant, missense	RNF213	GRCh38.p7	17:80319364	TCACAGCTGTGTTCT[A/G/T]CCATGACCCAGCTAA	57674
rs747293119	snp	A/G	0.000123419	0.00785456	intron-variant	RNF213	GRCh38.p7	17:80336444	TAGCAACGTTAGGGC[A/G]GTGACTGTGGAAATG	57674
rs747293195	snp	C/T	4.94189e-05	0.00497062	intron-variant	RNF213	GRCh38.p7	17:80343810	TTAGAGTTGGGAGAA[C/T]TCGCCATCGTGTCGT	57674
rs747303879	snp	C/T	1.69238e-05	0.00290888	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383627	GTGTTACAATCTGTT[C/T]GTAGCAATACCTCAC	57674
rs747309939	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352244	ATTATTGTTAACCTC[A/G]AGAGGATTCTTTCCA	57674
rs747341031	in-del	-/C	1.69563e-05	0.00291168	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376583	GCCTTCACTGGAACA[-/C]CCCCCCAGAGCTTGT	57674
rs747361450	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80306267	GAGTTCCCTACTTCA[A/G]TTTATGAGAGAGAAG	57674
rs747381395	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314742	GAGGTGATGGTGGTG[A/G]TGGTGATGGTGGAGG	57674
rs747389177	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373370	TGGTGCCACTGCTTC[C/T]GCGTTCCGCCTGCCC	57674
rs747400508	snp	C/T	1.64846e-05	0.0028709	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364420	GTGAGTGAGTGGCGC[C/T]CTCTTTTGACAGAGC	57674
rs747426139	snp	C/T	0.000117793	0.00767349	missense	RNF213	GRCh38.p7	17:80348183	TCGCAGCGGAGTGGC[C/T]GTCGCAGGAGTACTT	57674
rs747428368	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80335850	GGCGTGGTGGTGGGC[G/T]CCAGTAATCCCAGCT	57674
rs747436887	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396669	TTCATTAAGTTCAAC[C/T]ATTACCATTACGAAT	57674
rs747439820	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80293126	GCAGTGGCACGATCT[C/T]GGCTCACTACAGCCT	57674
rs747442335	snp	C/T	3.30568e-05	0.00406538	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369770	TTTCTGGTTTAAGGA[C/T]ACTGTGAACACACAA	57674
rs747447421	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334499	ACCTTGCCACACCCC[A/G]CCACTTCGGAAGCTG	57674
rs747455758	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80267338	CCCAGCTACTCGGGA[C/G]GCTGAGGCAGGAGAG	57674
rs747459356	snp	G/T	1.64784e-05	0.00287035	intron-variant	RNF213	GRCh38.p7	17:80349755	GCAAGTAATTTGCAT[G/T]TCTTAACTCTGTAGA	57674
rs747465054	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372371	TAAAAAGGAATGTTA[C/G]GTTTCCATAAGTCAA	57674
rs747467326	snp	C/G	0.000114976	0.0075812	intron-variant, missense	RNF213	GRCh38.p7	17:80278905	CCTTCTGCAGACTGT[C/G]AGCAGGTAGTCCGAG	57674
rs747471717	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393122	AGCTTCGGACTATAG[C/G]CATACACCACCACGT	57674
rs747482273	snp	A/T	1.64768e-05	0.00287021	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361797	GGTTTCTTGCCCAGC[A/T]CCATGGAGAGCCGCA	57674
rs747494709	snp	A/G	1.67108e-05	0.00289052	missense	RNF213	GRCh38.p7	17:80347312	AGTGGCAAGGATGAC[A/G]TCCAAGCTTTGGACA	57674
rs747501707	in-del	-/GGAGTTTTTTTGTAGGGCTTTTAA	1.70664e-05	0.00292112	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382964	GTAACCTACACATTT[-/GGAGTTTTTTTGTAGGGCTTTTAA]ATTTTGACACAGAAT	57674
rs747510623	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383156	GCTCCTTGCCTGTTG[C/T]CCCTCGTAGCGGTGC	57674
rs747519394	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80289592	GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAA	57674
rs747523880	snp	G/T	1.67975e-05	0.00289802	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372701	TGCCTCGACAGAGCT[G/T]CAGATTTCCTCTCGG	57674
rs747525866	snp	A/G	1.6676e-05	0.00288751	missense	RNF213	GRCh38.p7	17:80340270	TGGCAGGTCACTACC[A/G]GGTCCCGAAGCAGAC	57674
rs747533359	snp	A/G	1.70061e-05	0.00291595	missense	RNF213	GRCh38.p7	17:80340132	CGCAGCAGCACCGAG[A/G]AGACTACCAGCTCGT	57674
rs747538125	snp	G/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80309072	GTGTCTGAAACTGCA[G/T]GAAGCCATCTGCAGC	57674
rs747543753	snp	A/G	1.65209e-05	0.00287405	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380788	GCAGCGTGCCAAAGC[A/G]GCCAGCCTCAGCCTC	57674
rs747543791	snp	C/T	3.29647e-05	0.00405971	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375856	CACAATGCAAGCCTC[C/T]ACCCCACGCCAGAGG	57674
rs747545067	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266158	CAAAAGGTGGCCCAC[C/T]TTACTAGGCGTGGTG	57674
rs747545165	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277746	TCCCACAGGGAGCCT[A/G]TTGAATTCTGAAGCT	57674
rs747561880	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379125	TGAGCCTGGGGAGGT[C/T]AAGGCTGTAGTGAGC	57674
rs747565182	snp	C/T	1.64868e-05	0.00287109	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364478	ACTCTTCGTGGAGCA[C/T]GTGCTCCTAGGAACC	57674
rs747570217	snp	A/G	1.68023e-05	0.00289843	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388568	CTGCTGGAAATGTCC[A/G]CGATGGATTTAATTT	57674
rs747598702	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391461	ATTTTAGTACAGAGA[C/G]GGGGTTTCTCCACGT	57674
rs747606017	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80337886	GAGCCCTGGCAGCCA[C/T]GAGGAGTCACGAGAG	57674
rs747613172	in-del	-/TTTAT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357612	ATCGTCATAATTTTA[-/TTTAT]TTAGAGAACCTCGAT	57674
rs747613651	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	RNF213	GRCh38.p7	17:80319270	CAGTGTGGCCAAGAC[C/T]TTCGAGAAATGCATC	57674
rs747625978	snp	C/T	3.32967e-05	0.0040801	synonymous-codon	RNF213	GRCh38.p7	17:80273323	GAAGGAGGAAGGGGG[C/T]CCGTGCTTGTTCCCG	57674
rs747648636	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80304711	TATATCCCTTTTATT[A/G]TAAAATATACATAAT	57674
rs747648727	snp	G/T	1.64827e-05	0.00287073	missense	RNF213	GRCh38.p7	17:80307128	TTTTCTCTGCCTTAG[G/T]ATGTTCAGGATGTTC	57674
rs747662744	in-del	-/G	1.68023e-05	0.00289843	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372621	ATTCTCCAGCAAGCC[-/G]GGGCCGAGAGCCTGC	57674
rs747682194	snp	C/T	4.98384e-05	0.00499167	intron-variant	RNF213	GRCh38.p7	17:80344044	GGCGTTTTCGCCTGG[C/T]GTGGGGGGCTCTTGG	57674
rs747687436	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272427	GAGTAGGCCGACGGG[A/G]ATGCTGACAGCTGTG	57674
rs747717423	snp	A/C	1.66305e-05	0.00288357	missense	RNF213	GRCh38.p7	17:80273261	GAGAACAATAACTCC[A/C]CAATGGCGTCGGCCT	57674
rs747718803	snp	A/G	3.3264e-05	0.0040781	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354123	CAATATGCGGAGGGT[A/G]GTGCTCCTCCTGGGC	57674
rs747730072	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319052	GAGGACATGCTTTGC[A/G]TGGGCCAGGAGAAGC	57674
rs747745442	snp	A/T	1.65833e-05	0.00287948	missense	RNF213	GRCh38.p7	17:80295620	CCGGACGGAAAAAGC[A/T]CGGACTTTTTGCCTG	57674
rs747763913	snp	A/G	1.64765e-05	0.00287019	missense	RNF213	GRCh38.p7	17:80307195	TCCTGGACACTTACC[A/G]GGACAAGTAAGTGGA	57674
rs747766006	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80286592	GTGGCGCTTCCTCAT[A/C]CCCTTGTTACCAGTT	57674
rs747767262	snp	A/T	1.72172e-05	0.00293399	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372585	ACCACCTAGAAGAGG[A/T]AGGTCGTTTCCTTAA	57674
rs747767551	snp	A/G	7.86318e-05	0.00626975	missense	RNF213	GRCh38.p7	17:80340084	GCTACGAGGTGGCAC[A/G]CCAAGCGGAGGAGCT	57674
rs747771072	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390671	CAAAGTGCTAGAATG[A/G]AAAGGCGTGAGCCAC	57674
rs747771801	snp	A/G	1.66974e-05	0.00288936	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361688	AGGCAGGGGAGCGCC[A/G]TGACTTAGACGCACT	57674
rs747785477	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80340610	CAGTGTACTTTGTGG[-/TT]TTTTTTTTTTTTTTT	57674
rs747791161	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365824	GCACAGGGCTTTCAG[C/T]CAGGTCCAGCGTGGG	57674
rs747798482	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365343	CGGCTTAGACACAGT[A/G]TCAGCTGATTTCCCA	57674
rs747799712	snp	A/G	1.64814e-05	0.00287061	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361754	CCCAAGAAGTTCGTG[A/G]ACATCTTTCAGCAGA	57674
rs747802496	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388517	GGCAGCGCGGCACTA[C/T]GCTGCAGTTTTCCGG	57674
rs747816525	snp	A/C	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375770	TGCAGGCCTGCAAGA[A/C]CCCCCAAAGCCAGCA	57674
rs747829918	snp	C/G	1.64836e-05	0.0028708	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385205	AGGACCAGGACTGTC[C/G]CGCATTTGGCGGTTC	57674
rs747846267	snp	C/G	5.0234e-05	0.00501144	intron-variant	RNF213	GRCh38.p7	17:80295539	GGTTCATGCATCTTC[C/G]TCTTCTCCCACCATC	57674
rs747846518	snp	A/G	1.65168e-05	0.00287369	missense	RNF213	GRCh38.p7	17:80298421	TGCTGTATGGAGCTG[A/G]CCCCGCGGCACAAGG	57674
rs747847979	snp	A/C	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385106	GGGATCTAGTGAAGC[A/C]GTTCCAGAACGTCCA	57674
rs747878410	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270436	ATCTCTTCAAATCCC[C/T]TGCACAAAGCTTCTC	57674
rs747883098	snp	A/G	1.64928e-05	0.00287161	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388663	TATGAACATCTCTTT[A/G]TGGACATCAAGAACA	57674
rs747894921	snp	A/G	9.8881e-05	0.0070307	missense	RNF213	GRCh38.p7	17:80346301	TTCCACGAGCACAGC[A/G]CGATGCTCTTAGCGC	57674
rs747899210	snp	A/C	1.65173e-05	0.00287374	synonymous-codon	RNF213	GRCh38.p7	17:80313059	TAATTCAGTCCAAAC[A/C]GTCTTCCAAGGGACC	57674
rs747902351	snp	A/C	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389875	TGCCCTCTGGCAGTT[A/C]CTGTCTGCTCATAAG	57674
rs747922251	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RNF213	GRCh38.p7	17:80345250	GGAGCCTCACCCATA[C/T]GTTTTCTTCAATGAC	57674
rs747926576	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386685	GCTGTCTTTCTGCCC[C/G]TCAGCTATTCCGTGG	57674
rs747928559	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80350588	AGAAAAGGCCAATAA[C/T]ATTACAAAAATAGTG	57674
rs747933591	snp	C/T	3.64133e-05	0.00426677	intron-variant	RNF213	GRCh38.p7	17:80350427	TTTTCTCAGAAACTA[C/T]GTAAAAAACCCAAAA	57674
rs747975259	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80308901	TTAACCTAGATAAGG[C/T]CAAACAAATGCCCTG	57674
rs747984239	snp	C/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80290584	GCACGCTGAGCCCGG[C/G]TGGAGGAGTCACCGT	57674
rs747986417	snp	C/G/T	4.97693e-05	0.00498824	missense	RNF213	GRCh38.p7	17:80350326	ACGAATACAGCCAAA[C/G/T]GTAAAATCCTCATTT	57674
rs747987633	snp	C/G	1.64746e-05	0.00287002	synonymous-codon	RNF213	GRCh38.p7	17:80346249	CAGCTTTGTCAGCCT[C/G]AGGGACGTGGAGCGC	57674
rs747989175	snp	C/G	1.69836e-05	0.00291402	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363590	CCGCTCAGCCACGCC[C/G]TGCTGTCCGTCTCCC	57674
rs747994707	snp	A/G	1.66599e-05	0.00288611	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372664	GGTTGAATACCTGCA[A/G]GAGGTGGCCCGGATC	57674
rs748007411	snp	C/G	1.71578e-05	0.00292893	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373154	TTTCCCAAGGACGTT[C/G]TCAAGCAGCAGGTGA	57674
rs748015426	snp	A/C/G	8.23643e-05	0.0064169	intron-variant	RNF213	GRCh38.p7	17:80343819	GGAGAACTCGCCATC[A/C/G]TGTCGTGTGTTTACA	57674
rs748021061	snp	A/C/T	5.2142e-05	0.00510576	missense, synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288132	TGAGGCTCAGAGCAG[A/C/T]CCGCAATTCCAGGAC	57674
rs748031080	snp	C/T	3.29462e-05	0.00405857	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367817	CGCACTCTCTGTGAA[C/T]GCAAGGAGACAGCCA	57674
rs748037692	snp	G/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80386055	AAACCCTCAGTACTC[G/T]TCAGTCCCTAAATAT	57674
rs748056979	in-del	-/G	8.2392e-05	0.00641788	intron-variant	RNF213	GRCh38.p7	17:80349735	CAACCTTTCCTTGAA[-/G]TCTGGCAAGTAATTT	57674
rs748063465	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80264720	AGCAGACAGTCAAAC[A/C]ACAGACCCCCTTACA	57674
rs748081556	snp	C/T	0.000115307	0.00759211	intron-variant	RNF213	GRCh38.p7	17:80306241	TCTCCGTCCCTATTT[C/T]TCTTATGCAGGAGTT	57674
rs748091540	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80323251	GTGATCTACTTGCCT[A/G]TCCTTGTGTCAGTAC	57674
rs748113405	snp	C/G	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80290643	TTCCCATTCAATCCT[C/G]ACCTCCATAAAGTCT	57674
rs748122501	snp	A/G	1.65151e-05	0.00287355	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376510	ACTCTTGGAGCCCCT[A/G]AAGAATCTGGCCTTC	57674
rs748133732	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394574	TAATTTCTCTTCCTA[C/G]ACAGCTCAGCACAGC	57674
rs748139166	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80280161	AGGCAGCGTCCACAC[A/G]GGGCTGGACTTAGCC	57674
rs748152334	in-del	-/TG			intron-variant	RNF213	GRCh38.p7	17:80261917	ACCTACTTGGGAGAC[-/TG]AGGCGGGAGAATCGC	57674
rs748177583	snp	A/G			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321777	CACCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTT	57674
rs748179402	snp	A/G	1.67556e-05	0.0028944	missense	RNF213	GRCh38.p7	17:80346725	ACTCAGATCTCTTCC[A/G]CAGCCTGAAGCAGGT	57674
rs748186436	snp	A/G	7.41359e-05	0.00608789	missense	RNF213	GRCh38.p7	17:80343314	CTCTTTCACCTGGAC[A/G]TGACCTCCTCAGTAA	57674
rs748198399	snp	C/T	1.64765e-05	0.00287019	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374437	CCCATTGTTCACCCC[C/T]AACTAACCTCTGTAT	57674
rs748198736	snp	A/G			missense	RNF213	GRCh38.p7	17:80332608	AACGGTGACTTCAGT[A/G]TTCTCAACACTTTAC	57674
rs748206837	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383727	CATCAGCCAAGATAA[A/G]CGTATCAGCTCTAAC	57674
rs748214252	in-del	-/TATT	1.66054e-05	0.00288139	intron-variant	RNF213	GRCh38.p7	17:80351828	GAACATCAGTCAGGG[-/TATT]TATTTATGTATTTAT	57674
rs748223694	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393750	TCATTGAGAGATGAC[A/G]ATGAAGATTAGATGA	57674
rs748227530	snp	G/T	1.65045e-05	0.00287263	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386672	CTGGACGCTGAGCGC[G/T]GTCTTTCTGCCCCTC	57674
rs748228521	snp	A/G	0.000151343	0.00869763	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360016	TCTTGTGTTTTGAGT[A/G]ACGTCTCACAAACCC	57674
rs748230137	snp	A/G	3.39179e-05	0.00411798	intron-variant	RNF213	GRCh38.p7	17:80291873	CCCTCCGGAGTGCAG[A/G]TGCCAATCCCGCGGT	57674
rs748231907	snp	C/G			missense	RNF213	GRCh38.p7	17:80336354	GAAGGCTCTGGATAA[C/G]GACCAGTACCTGCCC	57674
rs748240232	snp	C/T	1.65086e-05	0.00287298	utr-variant-5-prime, intron-variant	RNF213	GRCh38.p7	17:80263645	CAGCGACTCCTGCTC[C/T]TGCTTCTGGATCTGC	57674
rs748241428	in-del	-/AAAA			intron-variant	RNF213	GRCh38.p7	17:80272306	ATAATAAAATAAAAT[-/AAAA]AAAGAAAAAGAAAAA	57674
rs748247392	snp	A/G	4.9611e-05	0.00498026	missense	RNF213	GRCh38.p7	17:80346811	ACCTTCCGGCAGTGC[A/G]CCCGCTTTCAGCAGG	57674
rs748258154	snp	C/T	4.95135e-05	0.00497537	missense	RNF213	GRCh38.p7	17:80347882	ACGGTGCTGGAGAAA[C/T]GGCAGAAGAGCATCG	57674
rs748281903	snp	A/G	1.65633e-05	0.00287774	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358482	TGAATAATGAAAGGT[A/G]AGTGGAAGGCTTTCT	57674
rs748286898	snp	C/T	3.29549e-05	0.00405911	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369654	TCCAAAAGGGGCGCT[C/T]AAGAGATGCTGCCCA	57674
rs748288455	snp	A/G			missense	RNF213	GRCh38.p7	17:80339816	ATGGGTGGGTCTCCC[A/G]TGGAGCGTTGTCTCC	57674
rs748290042	snp	C/T	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80306346	CTGCTACCTCTGAGT[C/T]ACCTGGTTATGTATA	57674
rs748314818	snp	A/G	1.64879e-05	0.00287118	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353607	GTGGCAGAGGAGGCC[A/G]TGGAAACAGAAAGTT	57674
rs748318105	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380800	AGCGGCCAGCCTCAG[C/G]CTCTGTCTTGTGTTC	57674
rs748320525	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80263495	CACAGAGCGGGGAGG[A/G]GCTGGGCTTGGGCTG	57674
rs748331395	snp	A/G	1.65241e-05	0.00287433	intron-variant	RNF213	GRCh38.p7	17:80289644	TCAAGGTCAGGGTTT[A/G]GTTCCTTGTTCCAGG	57674
rs748337407	snp	G/T	3.30819e-05	0.00406692	intron-variant	RNF213	GRCh38.p7	17:80348289	CATCTTCACAGAGGT[G/T]ATTGTCTTTCTGCAC	57674
rs748343121	snp	C/T	4.94385e-05	0.0049716	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380888	CCCGCAGCGGAGAGA[C/T]GTGGTGACATGTGAC	57674
rs748343272	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368793	CTGAGGATCAACCCA[C/T]TTCTTGTCTAGCTTT	57674
rs748352888	snp	C/G	1.64846e-05	0.0028709	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288792	CGGCTCCAGGAGGCC[C/G]TCTCCTGCCCACGGC	57674
rs748370683	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80301328	GATAAATGGGATTAC[A/G]TCAAATCAAAAAGCT	57674
rs748376526	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80285687	TGCTTTTTTTTTTTT[-/G]TGAGATGGAGTCTTG	57674
rs748382813	snp	A/C/G	3.29605e-05	0.00405948	intron-variant, missense	RNF213	GRCh38.p7	17:80319380	CCATGACCCAGCTAA[A/C/G]GGCTATGAAGCACCC	57674
rs748382874	snp	A/C/G	0.000228944	0.0106972	missense	RNF213	GRCh38.p7	17:80337966	CTGGCAAGAAGGATC[A/C/G]TAACAACACGGAAGT	57674
rs748392937	snp	A/T	1.64757e-05	0.00287012	intron-variant	RNF213	GRCh38.p7	17:80309001	GCCGGGATTTCTCTT[A/T]ACTCTTTGCGGGGCA	57674
rs748409416	in-del	-/A	1.70377e-05	0.00291865	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376954	GTCTGGAGCGAGTCC[-/A]ACTGGTACAGTAAGT	57674
rs748420195	snp	C/T	1.67581e-05	0.00289461	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385616	GGAGATCGCTTGAGA[C/T]GAACGGTTAGTATCC	57674
rs748428180	snp	C/G	1.66286e-05	0.0028834	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354081	CGCCGTGGGCATGCT[C/G]AGAGACCAGAACGAG	57674
rs748443071	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279968	CTGCCTTCCCCGCAC[C/T]GCGCTCCCCCCAGCC	57674
rs748443523	snp	C/G/T	3.30252e-05	0.00406346	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393518	ATTTCCTCAGCTATC[C/G/T]TTGGATGACTTTGGA	57674
rs748443934	snp	C/T	3.29614e-05	0.00405951	missense	RNF213	GRCh38.p7	17:80345897	CTGGCCTGCATATTA[C/T]AGCTGCCTGCAATCC	57674
rs748454069	snp	A/G	3.2956e-05	0.00405918	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379693	TTGACCACAAACCTC[A/G]GGACGGCTTTCATCT	57674
rs748459913	snp	C/T	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80345045	CTCTCTTCTGCAATC[C/T]GAGTTTTATTGGCGA	57674
rs748459923	snp	A/C	3.3699e-05	0.00410467	missense	RNF213	GRCh38.p7	17:80340285	GGGTCCCGAAGCAGA[A/C]CCTGTCGGCGGCAGC	57674
rs748467454	in-del	-/C			frameshift-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288001	GGCCAGCCGAGCCAG[-/C]CCCCAGGCACAGCCA	57674
rs748487919	snp	C/G			synonymous-codon	RNF213	GRCh38.p7	17:80317271	CATGGAATGGAGGCT[C/G]ACAAAGGTACCAAAA	57674
rs748499578	in-del	-/CTT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372340	TTCACTTTTCCCCTC[-/CTT]CTTGTCCTTAAAATA	57674
rs748500875	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317365	CCAAGAGATCTCAGC[A/G]GTGCCTCTCTGTGGG	57674
rs748508079	snp	C/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80309081	ACTGCATGAAGCCAT[C/G]TGCAGCAGCACAAAG	57674
rs748516466	snp	C/G	8.29552e-05	0.00643978	missense	RNF213	GRCh38.p7	17:80289731	AATGAACAAGGGGAG[C/G]CTGAAGACCTCAAGA	57674
rs748521764	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285395	TACCAGGCAGCTGGC[C/T]GGGCAGGGACGGCGT	57674
rs748531911	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259669	CAGGTGCACCACCAC[A/G]CCCAGCTAATTTTTT	57674
rs748566995	snp	C/G	3.35751e-05	0.00409712	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287779	TAGAGTAGAGTAAAT[C/G]TAAGAAATAAAGTGA	57674
rs748579281	snp	C/G	3.29745e-05	0.00406031	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361892	GAGGAATTAAAGGTA[C/G]ATGTTTAGATACTGG	57674
rs748586136	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326094	CTCCCAAGTAGCTGG[A/G]ATTACAGATGTGAGC	57674
rs748588865	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326708	CGTATTTATGTTTCC[C/T]CCATGTCTTTTCATG	57674
rs748610206	in-del	-/AC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381862	GGAAAGAATGAGAGA[-/AC]ACACAGAGAGAAAAC	57674
rs748611334	snp	A/C/T	0.000132783	0.00814711	missense	RNF213	GRCh38.p7	17:80295606	ACGTGGTACCATTGC[A/C/T]GGACGGAAAAAGCAC	57674
rs748612639	snp	A/G			missense	RNF213	GRCh38.p7	17:80294887	CAGACCTGGGACACC[A/G]TCAACCTGAACAGCT	57674
rs748616733	snp	C/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354531	TGGAGTGGTTGGCAA[C/G]GGAAGCCTGCAACCA	57674
rs748624950	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397684	TCACTCGGGGAGCTC[A/G]GTTGTTGGAGACATG	57674
rs748631634	snp	C/T	3.34818e-05	0.00409143	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373028	AAGCAGTTCTGTATC[C/T]GGGTGGAGAACGACT	57674
rs748637235	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268704	CATTCATCCATGTAC[C/T]TATCCATCCATCTTA	57674
rs748642172	in-del	-/TCTT	1.80838e-05	0.00300692	intron-variant	RNF213	GRCh38.p7	17:80298304	CAGCTCACTGCGGGA[-/TCTT]TATTCCCTTCCAGCT	57674
rs748643960	snp	A/G/T	0.00046463	0.0152348	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374726	TGTATTGGAAGTCAC[A/G/T]TGCCCACAGCCTCCA	57674
rs748648436	snp	A/G	1.66313e-05	0.00288364	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354611	CAAGGAGTGGCTCCA[A/G]TCTGGTGGCAGCATG	57674
rs748659121	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80308428	TCCTGAGTCCCTCCC[-/A]AGGCTCCTCCTGAGT	57674
rs748659330	snp	A/G	0.000115788	0.00760792	missense	RNF213	GRCh38.p7	17:80332162	TGGCTGGGAAGATAG[A/G]CTTGCTCAGAGACAG	57674
rs748666763	snp	C/T	9.89511e-05	0.00703319	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368111	AACTGCCTTGCCAGA[C/T]GAATTCTCTCCAGCT	57674
rs748669195	snp	C/T	1.72907e-05	0.00294025	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363091	ATTCTAAAAGCTTTT[C/T]TGAATCCCAGTTTCT	57674
rs748678987	snp	C/T	1.65165e-05	0.00287367	missense	RNF213	GRCh38.p7	17:80298419	ACTGCTGTATGGAGC[C/T]GGCCCCGCGGCACAA	57674
rs748684402	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376314	AGCAATGTGAAGCTG[C/T]GAGCAAATTCATTGG	57674
rs748698643	snp	A/G	1.64868e-05	0.00287109	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372926	TTGTGTCCTACAATA[A/G]ATGCCCTAAGTCACC	57674
rs748701727	snp	A/T	1.65018e-05	0.00287239	missense	RNF213	GRCh38.p7	17:80346416	TCGGGGTGTGTTACC[A/T]TGCCTCTTTAGAAAA	57674
rs748728507	snp	A/G	3.65724e-05	0.00427608	synonymous-codon	RNF213	GRCh38.p7	17:80340118	CCACAATCTGTGCAC[A/G]CAGCAGCACCGAGAA	57674
rs748729822	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377141	AGGAGCTGGCACTCC[A/G]CCGGCTAGATGATCC	57674
rs748731097	snp	C/G/T	5.15711e-05	0.00507773	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354203	TTGCCCCTGCCCCCA[C/G/T]GTGGGCTCTTCCTGA	57674
rs748734616	snp	A/T	6.72981e-05	0.00580039	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372617	GCATATTCTCCAGCA[A/T]GCCGGGGCCGAGAGC	57674
rs748735262	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384007	GCCCTGGGCTTTTAC[A/G]TAGTATAATCATTCT	57674
rs748737421	snp	C/T	1.68323e-05	0.00290101	synonymous-codon	RNF213	GRCh38.p7	17:80347287	TGCACAGGCTGTCCT[C/T]AGGAACTTCAGTGGC	57674
rs748738296	snp	C/T	4.94686e-05	0.00497311	synonymous-codon	RNF213	GRCh38.p7	17:80347515	GCAGCAGACATTCTT[C/T]GAGGGGGACCAGCAG	57674
rs748741549	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80349056	TGGAACCGAGAGATA[A/C]TCAGGAGGCAATTTG	57674
rs748755081	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80335976	AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA	57674
rs748755648	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80333738	AATCCCATCCATTTA[C/T]ACTTGAACCCTAGTG	57674
rs748757110	snp	C/T	1.66971e-05	0.00288934	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389125	CCAGGTGGTGAGATG[C/T]CAGAAACCCAGCCCA	57674
rs748786909	in-del	-/TG	4.94328e-05	0.00497131	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376479	CTGCAGCCGTCCTTC[-/TG]TGTGGACAGAATGAA	57674
rs748790924	snp	A/G	8.23811e-05	0.00641746	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361863	TTCTCTTGACCATGC[A/G]TGTGTCAACGGAGGA	57674
rs748810404	snp	C/T	1.6495e-05	0.0028718	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388706	TGATCCCGATAAACC[C/T]GATCCTGTGCACGGG	57674
rs748813859	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267461	AAGAAAAAAAGTGCT[A/G]CTCCAATGAACACAC	57674
rs748824881	snp	A/G	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80290653	ATCCTGACCTCCATA[A/G]AGTCTTCATCAGAGG	57674
rs748825110	snp	A/G	5.30363e-05	0.00514931	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351634	TATTTGCTTGTTTTT[A/G]TGTGTGTGTTTGTTT	57674
rs748850620	snp	C/T	1.64768e-05	0.00287021	missense	RNF213	GRCh38.p7	17:80344837	ACTTTCCAAAGACCT[C/T]ACCAGTATTTAAGAC	57674
rs748858146	snp	C/G/T	1.64781e-05	0.00287033	intron-variant	RNF213	GRCh38.p7	17:80308986	TTCTCCTAAATCCTT[C/G/T]CCGGGATTTCTCTTA	57674
rs748865693	snp	C/T	1.64961e-05	0.00287189	synonymous-codon	RNF213	GRCh38.p7	17:80313146	TTCAGGTGCCTCATT[C/T]ACATACGTCAAGGAA	57674
rs748878775	snp	A/G	1.64844e-05	0.00287087	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354454	AGCCTCTTTCTTGCG[A/G]GTATCCAAGATGCGC	57674
rs748879359	snp	A/C	1.65836e-05	0.0028795	missense	RNF213	GRCh38.p7	17:80295640	CTTTTTGCCTGTGGA[A/C]TGCCCAGTGAGGAGT	57674
rs748880825	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392818	TGGTCTCGAACTCCT[A/G]ACTTCAAGTGATCCA	57674
rs748881363	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80306553	CTCAGGATTCTTATT[A/C]CTAAAAAACAGACAG	57674
rs748899468	snp	C/T	0.000237893	0.0109037	intron-variant	RNF213	GRCh38.p7	17:80273433	CTCGGCTCCCCTCCG[C/T]CCCCGCTCACTCTGC	57674
rs748901672	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277804	CTAAGCGCAGACGCC[A/G]CATTCTAACCATGGT	57674
rs748905579	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383362	CAGAATGTAATGTAC[A/G]AGGTAGAGAAATAAA	57674
rs748912687	snp	C/G/T	3.29469e-05	0.00405864	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367985	TCAGCCGTGCTCCAT[C/G/T]TGCCTGGGAGATGCA	57674
rs748925318	snp	A/G	1.64792e-05	0.00287042	synonymous-codon	RNF213	GRCh38.p7	17:80295715	TGAGCTTTTATTAGA[A/G]GGCAGCCTGGACTGG	57674
rs748931107	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369333	AACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCGGA	57674
rs748937258	snp	C/T	1.6483e-05	0.00287076	missense	RNF213	GRCh38.p7	17:80346314	GCGCGATGCTCTTAG[C/T]GCAGCTGAATGCCTT	57674
rs748945196	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80314256	AGGTACTGGAGGTGA[-/TGG]TGGTGGTAAAGGTGA	57674
rs748948762	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358128	GTTTTCTAGGACTTA[A/T]AAATGATGGAAATGT	57674
rs748957706	snp	C/G/T			intron-variant	RNF213	GRCh38.p7	17:80309489	TCAGGCAACGCCACG[C/G/T]GGAGAAGACGACTTT	57674
rs748966967	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330803	GGCATTGGGGTGACA[A/G]TTGGTGTGCTGGATG	57674
rs748968862	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288579	TTAAACCATTGAGTC[A/G]GAGTCACCCTGGCCC	57674
rs748968968	snp	A/G	1.64795e-05	0.00287045	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381622	ATCCTGAAGGACCTG[A/G]AGCAGTTGGCCAAGA	57674
rs748970661	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391574	CTTTTTCTTTTGCGC[G/T]TTGTCTCTGTAATGG	57674
rs748972533	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376645	CTCTTGAGCATCTTT[A/G]TCTCCTCAGTTCTCT	57674
rs748980291	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329403	CTCCACAGTGTGGCT[A/G]TGTATGGAGAAGTCC	57674
rs748987196	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392193	GTCTTCCTCACCAAT[A/G]TGTTTCCTATTTGCT	57674
rs748991407	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80290596	CGGGTGGAGGAGTCA[C/T]CGTGTTCTTCCACGC	57674
rs748996205	snp	C/T	1.66037e-05	0.00288125	synonymous-codon	RNF213	GRCh38.p7	17:80340250	CGAGGCCATCCAAGC[C/T]TACCTGGCAGGTCAC	57674
rs749022353	snp	C/T	1.6522e-05	0.00287414	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385556	GGTTGAGGCAGCTGC[C/T]TCACAACAGGATCAC	57674
rs749025839	snp	A/C/G	8.2364e-05	0.00641686	intron-variant	RNF213	GRCh38.p7	17:80343824	ACTCGCCATCGTGTC[A/C/G]TGTGTTTACACCTCG	57674
rs749038442	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367173	CGTGGTATCATTGAT[A/G]TCAAGTTTTAAAACA	57674
rs749053371	snp	C/T	3.39029e-05	0.00411707	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288216	GTCCCAGGAGGGGAC[C/T]GGTCCCCCCACCTCT	57674
rs749060403	snp	A/G	0.000225729	0.0106214	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287899	CCCCTTTCTCCTGCC[A/G]GCCCCTGTCACCTGA	57674
rs749067103	snp	G/T	0.000297791	0.0121986	intron-variant	RNF213	GRCh38.p7	17:80313217	GTGACTGATCGTGAT[G/T]CCTCATGGCCTCAAA	57674
rs749068390	in-del	-/AA			intron-variant	RNF213	GRCh38.p7	17:80318236	CATTCTATTGGTAAA[-/AA]GACATTACTCCGAAA	57674
rs749069143	snp	C/T	1.65021e-05	0.00287241	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386683	GCGCTGTCTTTCTGC[C/T]CCTCAGCTATTCCGT	57674
rs749076966	snp	A/G	4.95282e-05	0.00497611	missense	RNF213	GRCh38.p7	17:80347897	TGGCAGAAGAGCATC[A/G]TGGAGGAGCTCTGTG	57674
rs749099369	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378707	CTTCAATCACTTCCT[G/T]GTCCATGAAATGAGG	57674
rs749117307	in-del	-/GTGTTTGTTTTTAAAATAGGTATT	1.65111e-05	0.0028732	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352905	CAGCCGGGAAAGACA[-/GTGTTTGTTTTTAAAATAGGTATT]CAAAGACAGTTGTGG	57674
rs749125149	snp	G/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287292	CCTGAGCCTGAGATT[G/T]CAAAACCAGCTTGGG	57674
rs749125216	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80267895	CTGGTCCTCAGCTCA[C/T]TGCAACCTCCGCCTC	57674
rs749134879	in-del	-/CT	0.000198511	0.00996073	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355127	TCTCTTTAAGACAGA[-/CT]CTCAGACCTCCTGCC	57674
rs749137021	snp	C/T	1.67877e-05	0.00289716	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360022	GTTTTGAGTGACGTC[C/T]CACAAACCCTCTTCT	57674
rs749145182	snp	A/T	4.96487e-05	0.00498216	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369796	CACAAAATCTCTCTC[A/T]CCATTCAATGATGTT	57674
rs749152414	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368075	GTTTGCCTCAGAGCA[A/G]ATGATATGCCCCTAC	57674
rs749159370	snp	C/T	0.000115841	0.00760968	intron-variant	RNF213	GRCh38.p7	17:80338012	GGTGAGGGCGCATCT[C/T]TGCAGTGGCGCTAAG	57674
rs749168681	snp	A/C	1.64991e-05	0.00287215	synonymous-codon	RNF213	GRCh38.p7	17:80306433	TCAGGGATTTACTAC[A/C]GGCTTCCGGGACTTG	57674
rs749178991	snp	A/G	1.68083e-05	0.00289894	intron-variant	RNF213	GRCh38.p7	17:80263809	GCTGGTGGAGGCTGG[A/G]GCAGTGGGGACCCCT	57674
rs749187452	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377662	ACAGTCATTCTCATA[C/T]TGTGGTCAGGGCCAG	57674
rs749192803	snp	A/G	1.66957e-05	0.00288922	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363633	GCATTTGCCGCAATG[A/G]CCTGCACGGAGATGC	57674
rs749225397	snp	A/C			synonymous-codon	RNF213	GRCh38.p7	17:80339659	AGTCATGGAAGAGCT[A/C]CCGCTGATGCTCTTA	57674
rs749226693	snp	C/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80294846	TTGCCGCTGCGCTCA[C/T]GCTGGACAGCACCTT	57674
rs749248484	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283311	GGGTGAGCCTGGGGC[C/T]GCTGCTCCGAGGTGT	57674
rs749252508	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80351185	GCACAGAACTCTTTG[C/T]TGAAATGGAAAGGTC	57674
rs749253996	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80312693	GGCGTGCTTTTCCCC[C/T]TCAGTCTCCTGGGCA	57674
rs749259167	snp	A/G/T	3.3573e-05	0.00409702	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376940	CTCGGAGGTGGAAGG[A/G/T]TCTGGAGCGAGTCCA	57674
rs749264200	snp	A/T	4.98269e-05	0.00499109	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358488	ATGAAAGGTGAGTGG[A/T]AGGCTTTCTTTCCCT	57674
rs749282694	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311235	CAATACTAAAATTAA[A/G]CAAAGCAAAAATACG	57674
rs749289267	snp	A/T	1.65089e-05	0.00287301	intron-variant, missense	RNF213	GRCh38.p7	17:80319436	TCAGAGATTGGGAAG[A/T]GGGCACCCTCCTCCC	57674
rs749294310	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361660	CATTCCCCTTCACTC[C/T]GGAGCCCCCTGGAGG	57674
rs749304335	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80343901	CAAGCTCCTCATTTT[A/G]CAATACTTAATGGAT	57674
rs749304997	snp	A/C	0.000114554	0.00756729	missense	RNF213	GRCh38.p7	17:80337722	CGCCCAAAGGTGGCC[A/C]AAAGGTGAGCGGTCC	57674
rs749305144	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80350911	GTCATTATTAATTTT[C/G]AATTATACAATTTGA	57674
rs749321968	in-del	-/TTTA			intron-variant	RNF213	GRCh38.p7	17:80299538	ACCAGAGAAAGTTTA[-/TTTA]TTTATTTATTTATTT	57674
rs749322052	snp	A/G	3.30246e-05	0.0040634	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383945	TATGTCTGGCTTACT[A/G]TGGCTCCCTCCCTCT	57674
rs749322415	snp	A/G	1.65089e-05	0.00287301	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380810	CTCAGCCTCTGTCTT[A/G]TGTTCTCTCGTTCTT	57674
rs749338327	in-del	-/T	1.64753e-05	0.00287008	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383729	CAGCCAAGATAAGCG[-/T]TATCAGCTCTAACCC	57674
rs749341025	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324449	TCGTGGTGTATAGTT[C/T]CTTTAACATGGGGCT	57674
rs749366825	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386139	GCAGAACCGAGACCC[A/G]GCTCCCGGCTGTGTG	57674
rs749371823	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80323406	ATTTTAGAATCAGTA[G/T]GTCAGTTTCCACTGA	57674
rs749374273	snp	A/G	5.0647e-05	0.00503199	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353980	TTTGCCCACTGTGTC[A/G]GTGGCAGAAACGGAT	57674
rs749374410	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80349796	CTCCAGGCTGCTAAC[A/G]AGTCACGACTGTGAA	57674
rs749378955	snp	A/C	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383850	CAGGAAAAGAATTAC[A/C]GTTGAGTACCTCCAG	57674
rs749379499	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395599	CAGAAGGAGTCCCCC[A/G]TGCCCTGCCTGAAAT	57674
rs749394993	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338769	GCCTGGCGATATGGT[A/G]AAACCCCATCTCTAC	57674
rs749404005	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366168	TGAGGCTGGCTCCCT[C/T]GGCCGGGCAGGAAGT	57674
rs749410766	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394686	AGAACTACAAAAATA[C/T]AAAATGCTTGTCCAG	57674
rs749421287	snp	C/T	1.6477e-05	0.00287024	missense	RNF213	GRCh38.p7	17:80294951	TGCAACAGCCTATGA[C/T]TTATGAAGGACAGGC	57674
rs749427375	snp	A/G	9.8881e-05	0.0070307	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353620	CCATGGAAACAGAAA[A/G]TTCTGAGAAGGTGGG	57674
rs749440727	snp	A/G	6.64452e-05	0.00576352	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371843	GTCTCCAGATCTGAG[A/G]GAACCAGGAATAATA	57674
rs749449733	snp	A/G/T	3.29453e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80345160	TGACCAAAGCCCGGG[A/G/T]AAGCACATGGTCACC	57674
rs749462254	snp	C/T	0.000247221	0.0111153	synonymous-codon	RNF213	GRCh38.p7	17:80349895	CGAGTACTCATTCCT[C/T]AAAGAAGTCCGGTGA	57674
rs749463905	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376330	GAGCAAATTCATTGG[C/T]GAATGCAAGATCCTT	57674
rs749466985	snp	G/T	1.66341e-05	0.00288388	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363114	CAGTTTCTGCAGATG[G/T]CTCTGTGGTCCTGCA	57674
rs749474704	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80272112	AGATGCTGAAACCCC[-/T]GTCTCTACTAAAAAC	57674
rs749475142	in-del	-/CA	6.59098e-05	0.00574026	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288584	CCATTGAGTCGGAGT[-/CA]CCCTGGCCCATTTTG	57674
rs749479458	snp	A/T	1.65007e-05	0.00287229	synonymous-codon	RNF213	GRCh38.p7	17:80347446	AGAGCAGGAAGATGC[A/T]GAGTCCCGCTACTTA	57674
rs749481957	in-del	-/CA	1.65525e-05	0.0028768	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389139	GCCAGAAACCCAGCC[-/CA]CAGACATCCCTCTCC	57674
rs749484420	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80304118	TGAAAAGTCTGCAGT[A/G]GCATTGTTCCTAAAG	57674
rs749499596	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80332973	GCAAAACACTTTGTC[A/G]GCTGCCCAACTGCAT	57674
rs749504308	snp	G/T	0.00263917	0.0362301	intron-variant	RNF213	GRCh38.p7	17:80340375	AGGAGAGCGGCAGGG[G/T]GGGCAGGCCCCGTCT	57674
rs749511769	snp	C/T	3.49785e-05	0.00418187	intron-variant	RNF213	GRCh38.p7	17:80298311	CTGCGGGATCTTTAT[C/T]CCCTTCCAGCTGGCG	57674
rs749511847	snp	C/G	1.64833e-05	0.00287078	intron-variant	RNF213	GRCh38.p7	17:80309193	GGAGTCAACACACAA[C/G]GTATCACACCCGGGA	57674
rs749528269	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80309101	GCAGCACAAAGCTAC[C/T]TAAGTTTTACGAGCT	57674
rs749538986	snp	A/G	3.31428e-05	0.00407066	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319491	TCTAGTTCTCTCCGG[A/G]TTCCTCAGTGTGCTG	57674
rs749571552	snp	A/C	1.64751e-05	0.00287007	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376271	CAATATTCTTTGATA[A/C]ATCTTAATGTTAAGT	57674
rs749578607	snp	A/T	3.29723e-05	0.00406018	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389295	CACAGCTGGTGGGGA[A/T]CCAAACATGCAGCTG	57674
rs749603018	snp	C/T	1.65979e-05	0.00288074	synonymous-codon	RNF213	GRCh38.p7	17:80346498	CGACAGCAGGCTGCT[C/T]CTGGATGAAATAACA	57674
rs749611698	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377521	TGGTATGGGCCTATA[G/T]TCTAATTGCTCTTTA	57674
rs749623272	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80302520	ATAGAAATATAACAC[C/T]GTTCCCCATAAATAT	57674
rs749632958	snp	A/G	1.64855e-05	0.00287097	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386354	GGCCTCTGTGCTACC[A/G]CTCTCGTCAGCTACT	57674
rs749634532	in-del	-/CTT	1.65187e-05	0.00287386	cds-indel	RNF213	GRCh38.p7	17:80298486	TCTGGAGGGACTCTC[-/CTT]CTCACCGTTCCGGGA	57674
rs749636418	snp	C/G/T	1.66474e-05	0.00288503	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390177	ACCCAAACCGAGGAG[C/G/T]GCTTCCGCCCTCAGT	57674
rs749651607	snp	A/C/T	3.39831e-05	0.00412197	intron-variant	RNF213	GRCh38.p7	17:80263821	TGGGGCAGTGGGGAC[A/C/T]CCTGGAGATGTCTCA	57674
rs749673751	snp	A/G	0.000158676	0.00890576	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389382	GGTGGGTCTCACACC[A/G]AAAAGGAAATCAGCA	57674
rs749680373	snp	C/T	1.67086e-05	0.00289033	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287993	GCCCCACTGGCCAGC[C/T]GAGCCAGCCCCCAGG	57674
rs749686830	snp	C/T	5.17308e-05	0.00508554	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288344	CCACCGAGCAACAGG[C/T]AGGGGCCTCAGCCTC	57674
rs749697705	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363176	CGAGGAAGAGGTTTC[C/T]TTACCGTGGGTGCAC	57674
rs749721052	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80317915	GGGGTCACCCGGACA[C/G]TTGAAGGATGGTGAA	57674
rs749724282	in-del	-/G	0.00024715	0.0111137	intron-variant	RNF213	GRCh38.p7	17:80309193	GGAGTCAACACACAA[-/G]GTATCACACCCGGGA	57674
rs749734369	snp	A/G	1.64773e-05	0.00287026	missense	RNF213	GRCh38.p7	17:80291774	ACCAGCAGAAGAAGG[A/G]CGAGTACGTCAACCG	57674
rs749735782	snp	A/G	3.34241e-05	0.0040879	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354159	GAATGAGGATGACGC[A/G]TGCCACGGTATGAGC	57674
rs749779063	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364955	GTCAGAGAATGCCAC[C/T]GGGGTTTGGGGTCTT	57674
rs749780384	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80291676	CATTGTCTGCATTTC[C/T]AAGAAGCACCTAGAT	57674
rs749783638	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379529	GTGCTCACGTCTGCC[A/G]GTGATAAGGAGGTGT	57674
rs749784001	snp	C/T	0.000214403	0.0103516	intron-variant	RNF213	GRCh38.p7	17:80319153	CTGGAGCGCTGCATC[C/T]GAAAGCTCTGAAACC	57674
rs749792455	snp	A/T	1.69963e-05	0.00291511	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363742	TCTGCTCCGATGAGC[A/T]CATGCAAGGCAGCGG	57674
rs749826497	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364231	CATCACAGTGGGACA[C/G]CGAGTCCCAGCTAAG	57674
rs749832315	snp	C/T	1.67086e-05	0.00289033	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373075	GGTGCGGAAGCTCAG[C/T]AGCCAGCGGGGGATG	57674
rs749844703	snp	C/T	1.66699e-05	0.00288698	synonymous-codon	RNF213	GRCh38.p7	17:80346561	TCTGAGGAAAACCAT[C/T]GCCAAGAACTTGGCC	57674
rs749870462	snp	A/C	1.65192e-05	0.00287391	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390137	GCTGCACGAAATGAT[A/C]ATCTTGAAACTAAAG	57674
rs749877909	in-del	-/A	1.65012e-05	0.00287234	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386688	GTCTTTCTGCCCCTC[-/A]GCTATTCCGTGGATG	57674
rs749897143	snp	C/T	1.68408e-05	0.00290175	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389358	TGATCAGACGATTCA[C/T]GTGTTAAAGGTGGGT	57674
rs749902434	snp	A/G	1.64746e-05	0.00287002	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389251	TGTGAAGTGCTGTCT[A/G]TCGTAGAAGTCACTC	57674
rs749909805	snp	G/T	5.92716e-05	0.00544355	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287937	TTCAAACCCGTGGCC[G/T]CAGGACACAGCCCTG	57674
rs749915184	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RNF213	GRCh38.p7	17:80345139	CACACCATCACTCCA[C/T]ACCTCTGACCAAAGC	57674
rs749920168	snp	A/G	1.64893e-05	0.0028713	synonymous-codon	RNF213	GRCh38.p7	17:80347503	ACTGCAGATCCTGCA[A/G]CAGACATTCTTCGAG	57674
rs749937102	snp	A/G	3.29495e-05	0.00405877	synonymous-codon	RNF213	GRCh38.p7	17:80309168	TAGACTTCTATCTCT[A/G]GTGGTAAGTGGAGTC	57674
rs749942925	snp	C/G	3.9816e-05	0.00446166	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363079	ATTTAAAAATATATT[C/G]TAAAAGCTTTTTTGA	57674
rs749963950	snp	A/C/G	1.85218e-05	0.00304311	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385668	TTCCAGGAGAGCCTC[A/C/G]TCTGAAAGCTCTTCT	57674
rs749966418	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394936	CGACTGCCTATGAAC[A/G]GGTGTGGGGGCCGGG	57674
rs749967919	in-del	-/TAT	4.95749e-05	0.00497845	splice-donor-variant	RNF213	GRCh38.p7	17:80295815	GGGATACCTCAGAGG[-/TAT]TATTATTTTTTGTCA	57674
rs749981934	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80305337	GTGTGCGCCACCACG[-/C]CTGGCTAATTTAGGA	57674
rs749997912	snp	A/G	2.13486e-05	0.00326708	missense	RNF213	GRCh38.p7	17:80289818	AACCAGGAAGCAGAT[A/G]TCCAGGAAGTGAAGG	57674
rs749999873	snp	A/G	2.52605e-05	0.00355382	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287854	AAAAAGAAGGGGAAC[A/G]AGTCCGCTTCCTCAG	57674
rs750006765	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279625	ACCTGCCACCACGCC[C/T]GGCTACTTTTTTTGT	57674
rs750008439	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394432	GACTCAGAGCACATA[C/T]AAAACCAGTTATGTT	57674
rs750015020	snp	A/C/T	6.58907e-05	0.00573948	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376304	TTTTCCTGTCAGCAA[A/C/T]GTGAAGCTGTGAGCA	57674
rs750017208	snp	G/T	1.64833e-05	0.00287078	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380923	GGCTGCCCCCAGTGG[G/T]CTTCCTCCTTATCCG	57674
rs750022999	snp	A/G	1.6476e-05	0.00287014	intron-variant, missense	RNF213	GRCh38.p7	17:80319316	TCAGCCTGCCAGGTG[A/G]ACAATCTCTCCTCCT	57674
rs750031507	snp	A/G	0.000369754	0.0135919	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355326	GAAGCGGGGTGAACG[A/G]TAATGGGGGCTTACA	57674
rs750036027	in-del	-/G	4.95458e-05	0.00497699	intron-variant	RNF213	GRCh38.p7	17:80307247	TCACATGCGGCCCCC[-/G]GGGGCTTCCTCTGAC	57674
rs750036991	snp	C/T			missense	RNF213	GRCh38.p7	17:80332407	GAGATTGATGTCATC[C/T]TCAAGGACTTTGTGA	57674
rs750039281	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259719	AGATGGGGTCTCTCT[A/G]TGTTGCCCAGGCTGC	57674
rs750041792	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80291644	GACTTGGGTCATGAC[C/T]GCGTTCTTGTTGAAG	57674
rs750045049	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370319	ATCCAAGAATAGTAT[C/T]ACCTGTGGTACTTGT	57674
rs750052505	snp	A/G			intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261122	CCGGCTGCGGGAGGG[A/G]TCGGGGTGGGGGCAG	57674
rs750099844	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381484	CCAATGGCCTCTACC[A/G]GGCTCACCATCTTCT	57674
rs750106383	in-del	-/C			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370665	GGGAAGCACACACAA[-/C]AACACTCCCACTACA	57674
rs750109133	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376374	TCAGCCGTTTTGCAA[C/T]ATCGCTCGTGGACAA	57674
rs750114968	snp	C/T	1.64855e-05	0.00287097	missense	RNF213	GRCh38.p7	17:80347600	TGCAGAAACATCAAT[C/T]GTGTGAAGATCTGCA	57674
rs750116000	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290508	GTGTGCGCGTGTGTG[C/T]ATGCACATGGCAGGT	57674
rs750116307	snp	A/C	6.58957e-05	0.00573964	missense	RNF213	GRCh38.p7	17:80345612	AAACTGGCTGTGGGA[A/C]AACCAGGCTTATTAA	57674
rs750124995	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80264191	CACGGTTTTTCTTCC[C/G]CTTGGGAATGAGAAG	57674
rs750128814	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377711	TCCCTTTTCAATGTG[A/G]GTCATTGGGTGAAAC	57674
rs750130178	snp	C/T	4.9675e-05	0.00498348	missense	RNF213	GRCh38.p7	17:80346476	GGTTCTTTCCGAAAC[C/T]GTATGACGACAGCAG	57674
rs750157173	snp	A/C	3.30546e-05	0.00406524	missense	RNF213	GRCh38.p7	17:80348057	GGCAGGGTCCCCGGG[A/C]CTTGACGGAGGAACT	57674
rs750165407	snp	A/G/T	3.47471e-05	0.00416804	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288409	TGGCACTGAGCCCTC[A/G/T]GCACCTGGGCTCTGC	57674
rs750180995	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80344570	ACATATTTTCAGTGC[A/G]TTTTTCATAAAGGTC	57674
rs750203855	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80301710	AATTAGTACTGCCAC[C/T]ATGGAGGACAGTATA	57674
rs750230960	snp	C/T	0.000114084	0.00755174	missense	RNF213	GRCh38.p7	17:80336232	GACATTGATGTGGAC[C/T]GGGTGGCCTGCTTCC	57674
rs750239349	snp	G/T	1.6664e-05	0.00288647	missense	RNF213	GRCh38.p7	17:80346535	CAGGATCTTTTTCTG[G/T]ACGGCGTACCTCTGA	57674
rs750250293	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378330	GCTGTGCGCCATGGG[A/G]GAAGAACTGTTGATT	57674
rs750264083	snp	G/T	1.6501e-05	0.00287232	intron-variant	RNF213	GRCh38.p7	17:80319141	TCCCATAGAGCACTG[G/T]AGCGCTGCATCCGAA	57674
rs750270490	snp	A/G	1.65004e-05	0.00287227	stop-gained, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352947	CTTCACAGGGCTGTG[A/G]CAGTCTGTCCACATC	57674
rs750286454	in-del	-/CCCTCCC	1.68508e-05	0.0029026	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367705	CCTGGCCGCCCTCAG[-/CCCTCCC]CCCTCCCCCCTGCTA	57674
rs750287033	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80343504	TCCTCCTTGTGTGAA[C/T]GTCATGGTGTGCGCT	57674
rs750290004	snp	C/T	1.66405e-05	0.00288443	missense	RNF213	GRCh38.p7	17:80273294	GAGGGTGAAATGGAG[C/T]GTGGGCAGGAGCTGA	57674
rs750292851	snp	A/C/G	4.53775e-05	0.00476309	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360232	CTCAAGACAGGTCAG[A/C/G]TTCAGCACAGGTGAA	57674
rs750303032	in-del	-/A	8.26973e-05	0.00642976	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372478	GGGGCATCCATGTTT[-/A]AAAAAAATAATATCC	57674
rs750313723	snp	A/G	3.29451e-05	0.00405851	missense	RNF213	GRCh38.p7	17:80291720	ACAAGTACGTCATTT[A/G]TAATGGGGAATCTTT	57674
rs750330925	snp	A/G	1.98191e-05	0.00314788	intron-variant	RNF213	GRCh38.p7	17:80317184	CTGTGTGCGGGTTTT[A/G]CAGGTCTGGAGGCGG	57674
rs750346938	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80344773	GGAGCTGAGTGCCCT[A/G]AGGAGTGACACAGAG	57674
rs750356808	snp	C/G	1.65938e-05	0.00288039	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375723	AAAAAGATGTGTTGA[C/G]CTTTTAAATTCTTAC	57674
rs750361615	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80285263	AAACTGAGGCCCACG[A/G]TGGCTCAGTGACCCA	57674
rs750364352	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80327242	GTGGTTCATGCGTAT[A/G]ATCCTAATGTTTTGG	57674
rs750371525	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281527	CCCCAACACACACAT[A/G]CCCCACTCATACCAC	57674
rs750379106	snp	C/T	1.65119e-05	0.00287327	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388638	TCTGGTGTACAGACA[C/T]GACTGGAACTATGAA	57674
rs750382020	snp	A/T	1.64779e-05	0.00287031	intron-variant	RNF213	GRCh38.p7	17:80344652	AGTCTTCTTGTAACC[A/T]TTTCATTAATGTCTC	57674
rs750386894	snp	C/T	1.64746e-05	0.00287002	stop-gained	RNF213	GRCh38.p7	17:80319205	GAGGAACCCCTCTCC[C/T]AGATCACTGCCTACT	57674
rs750408019	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377776	GCTTGTCCCAACGGC[C/T]ATCCTTGCTCCGTGG	57674
rs750408814	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363848	GCTCACCAGGAGCCT[A/G]CCAAGTGCCAGGCAT	57674
rs750410756	snp	C/G/T	6.82738e-05	0.00584234	missense	RNF213	GRCh38.p7	17:80347259	CAAATAGAAAGCCTT[C/G/T]CCCGCAAGACATTGC	57674
rs750418642	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337409	GTGACAGATCATGTT[A/G]TCAGGGTGGCACCTG	57674
rs750432066	snp	C/T	3.33183e-05	0.00408143	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393315	ATGCTGAGGAGACTG[C/T]TTTAAATGCTCTCTT	57674
rs750434761	snp	A/G	8.23771e-05	0.0064173	synonymous-codon	RNF213	GRCh38.p7	17:80345688	AAAGCTGGTCAAGGT[A/G]CACGGAGGAACAACT	57674
rs750445299	snp	A/G	1.65638e-05	0.00287778	missense	RNF213	GRCh38.p7	17:80295665	AGGAGTAAACTGAAA[A/G]CAGGCCTGATTGTCC	57674
rs750449941	in-del	-/GT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391475	ACGGGGTTTCTCCAC[-/GT]GGCCAGGCTGGTCTC	57674
rs750452307	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326329	TTAGAGCACTTTGAT[A/G]TGTACAGAAAAATTG	57674
rs750466126	snp	A/G	3.3561e-05	0.00409626	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354172	GCGTGCCACGGTATG[A/G]GCCTCCCCACCCCTC	57674
rs750471785	in-del	-/AG	1.66565e-05	0.00288583	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374588	TTAAGACTGCTCTGA[-/AG]GTAGGATGGGCCCGT	57674
rs750477230	snp	A/G	9.90835e-05	0.00703789	missense	RNF213	GRCh38.p7	17:80340030	CCCTGGGCTCCCTGG[A/G]GCACAAGGTCTACAG	57674
rs750486638	in-del	-/AAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362406	GGGTAAACGTTATAA[-/AAC]AACAATTTTATAATC	57674
rs750488710	snp	G/T	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80290558	CAGATTTCTGTTTTG[G/T]TTTTCCACCAGCACG	57674
rs750497230	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80284593	AATAATGGAAAGCCC[A/C]GCTCCACCTTTCTAA	57674
rs750512128	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295368	GAGCCCTGATGAGCC[C/T]CAGGGGCCCTGCCTG	57674
rs750520024	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398293	TTGTTTTGTGGTATG[C/T]GTGTAGGGTGAGCGT	57674
rs750539160	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375794	GCCAGCAGTCAGCCT[A/G]CTTCCTGTTAACACT	57674
rs750543832	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362731	ATATTTGGTTCACAG[C/G]GATGTCCTTTTCAGC	57674
rs750546005	snp	A/C	1.67781e-05	0.00289634	missense	RNF213	GRCh38.p7	17:80347155	TGCCAAAGCCTACGA[A/C]ACGGTGTGTAAGCGC	57674
rs750551749	snp	A/G	1.6489e-05	0.00287128	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361743	CTGCAGGACTGCCCA[A/G]GAAGTTCGTGGACAT	57674
rs750555493	snp	C/T	6.74582e-05	0.00580728	missense	RNF213	GRCh38.p7	17:80350389	GCCCAGCTCATTGCC[C/T]CAGCTAAGTATGTTT	57674
rs750560274	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80284856	CTCTGGAGAGAGGAA[A/G]CGCTTCCTCAAATCT	57674
rs750565435	snp	A/G	6.58903e-05	0.00573941	missense	RNF213	GRCh38.p7	17:80290610	ACCGTGTTCTTCCAC[A/G]CCATCATCTCTCTTC	57674
rs750580187	in-del	-/TCCATCCG			intron-variant	RNF213	GRCh38.p7	17:80269479	CATTCATCTATTCTA[-/TCCATCCG]TCTATCCATCCATCC	57674
rs750596095	snp	C/T	1.64955e-05	0.00287184	stop-gained	RNF213	GRCh38.p7	17:80313099	ACGAAAAGGTGGCTC[C/T]GAGAAGTTTTTACAA	57674
rs750597848	snp	C/G	1.90845e-05	0.003089	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372533	CAGGATTCAATACTT[C/G]AGAAGACCAGTGCTT	57674
rs750618954	snp	A/G	9.88354e-05	0.00702908	missense	RNF213	GRCh38.p7	17:80345315	TGCAGCCCAACATCA[A/G]CGGCAGTGTCGATGC	57674
rs750621319	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384344	CGTGGAAGACGGGAG[C/T]GAGTGGGTGTGTGCC	57674
rs750622401	in-del	-/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395876	CACCGGAAGACTCAC[-/T]TTGTCTGCCCTGCGC	57674
rs750628448	snp	C/T	1.65293e-05	0.00287479	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288042	GGAGGGTGACGGCCT[C/T]TCCGCGCCCACCGAG	57674
rs750635890	snp	A/G	3.33756e-05	0.00408493	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373065	GGGTGTACCTGGTGC[A/G]GAAGCTCAGCAGCCA	57674
rs750642087	snp	A/G	1.6641e-05	0.00288448	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381037	TAAGAACCTGCTTTC[A/G]CTTCTTCCCAGGGAG	57674
rs750675483	snp	A/G	0.000114123	0.00755303	missense	RNF213	GRCh38.p7	17:80327914	GTTGGTGACCTCCTA[A/G]GTGGCACGATTTTAG	57674
rs750688893	snp	A/G	1.7144e-05	0.00292775	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385494	GTTTGGCCCTTTCAG[A/G]GGGTTGCTATCATAC	57674
rs750689562	snp	A/G	1.64749e-05	0.00287005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367796	GGGCCTTTTGAGGCC[A/G]TGATGCGCACTCTCT	57674
rs750706811	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80345232	CCGGAAGAGGTGGGA[A/G]TCGGAGCCTCACCCA	57674
rs750707690	snp	C/T	3.29451e-05	0.00405851	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390000	GCTTCATTTGCTCTT[C/T]CGTCGTTTTAGGAGC	57674
rs750708688	snp	C/T			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383785	CCAGTGACCTTCCTG[C/T]CCCACCTGCCCCGGA	57674
rs750723932	in-del	-/T	1.6651e-05	0.00288535	frameshift-variant	RNF213	GRCh38.p7	17:80347329	CAAGCTTTGGACATC[-/T]TTTCTGGCCAATTTG	57674
rs750756103	snp	C/T	2.21565e-05	0.00332833	intron-variant	RNF213	GRCh38.p7	17:80343351	TCCAGCGTCAGCCGA[C/T]GGCCACATCAGTAAA	57674
rs750763313	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358686	GAGGCCGAGGCAGGT[C/G]GATCATGAGGTCAAG	57674
rs750769379	snp	C/G	8.26098e-05	0.00642636	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386656	GGCCCGCATGCCTGG[C/G]CTGGACGCTGAGCGC	57674
rs750793175	snp	C/G	1.64808e-05	0.00287057	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358445	TTCAGTGACACGATG[C/G]TTCTGAACATTCCTC	57674
rs750824702	snp	A/G	0.000167599	0.00915267	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288077	GCGACAGCCCCCTGC[A/G]GGCCCAGGCTTTGGG	57674
rs750835677	snp	G/T	1.8562e-05	0.00304642	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351672	AGGTATTCTTTTTTT[G/T]TTCTTTAAATAGGTA	57674
rs750847481	snp	A/G	4.99713e-05	0.00499831	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376549	CACCATGGCGGTAAG[A/G]GTAGGCCACAATTCC	57674
rs750848146	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319565	GAATCACGGCCGTGC[A/G]CGTGTGGCACAAGTC	57674
rs750850520	snp	C/G	1.65042e-05	0.0028726	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369741	CATGTCTCATGCAGT[C/G]AGCTGCCTTTTTCTT	57674
rs750853150	snp	C/T	4.94474e-05	0.00497205	synonymous-codon	RNF213	GRCh38.p7	17:80347746	TCTGGGGACCCACCG[C/T]GTCAAATGTCGGGTT	57674
rs750858343	in-del	-/TTCT	2.36013e-05	0.00343513	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351662	TTTTTAAAATAGGTA[-/TTCT]TTTTTTTTTCTTTAA	57674
rs750868192	snp	A/G	2.7284e-05	0.00369341	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353513	TGCTTCGACTGCAGT[A/G]GGCTTGGAACACCGG	57674
rs750884576	snp	C/G	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374492	CAGGCCAGATGGATA[C/G]GTACCTGGTGTACGG	57674
rs750892528	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391351	TCTTGGCTTAGTGCA[A/G]CCGCTGCCTTCTGGG	57674
rs750893752	snp	A/G	0.00114626	0.0239127	intron-variant	RNF213	GRCh38.p7	17:80337820	AGTGACTTCTAACCT[A/G]TGCTCTTCACAGATT	57674
rs750933923	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80329186	CGCCCCCCTCCCCCG[A/C]TACTCACTCCTGCTT	57674
rs750934746	snp	C/T	2.04463e-05	0.0031973	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373199	CAGCACACAAACATG[C/T]ACCCCCACAGCCCCA	57674
rs750955466	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386236	CTGCTTAAGCATAAC[C/T]CTGTCGTTTAAAGGT	57674
rs750962448	snp	C/T	1.64841e-05	0.00287085	synonymous-codon	RNF213	GRCh38.p7	17:80306303	TTTGCTGAGCATAGA[C/T]GAGCCTCTCTTCCGG	57674
rs750966575	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80299470	TTGGCAATATATATA[A/G]TCCTGATCTCTGATT	57674
rs750989626	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396983	GTGCTTCCCCTCACA[C/T]CTAAACTTACTATAA	57674
rs751003707	snp	A/C	3.31225e-05	0.00406941	missense	RNF213	GRCh38.p7	17:80346795	ACAGGGCATCATCAG[A/C]ACCTTCCGGCAGTGC	57674
rs751005876	in-del	-/TT	1.64749e-05	0.00287005	intron-variant	RNF213	GRCh38.p7	17:80309006	GATTTCTCTTAACTC[-/TT]TGCGGGGCAGGATTC	57674
rs751006111	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298220	GCGGTGCTCCTCTTG[C/T]TCTGTGTGCACGGTG	57674
rs751007535	snp	C/T	1.6504e-05	0.00287258	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383697	AGATAAAACCCTTCC[C/T]ACCATGAATAATCTC	57674
rs751009435	snp	C/G	1.65781e-05	0.00287902	missense	RNF213	GRCh38.p7	17:80263760	GGAGAGAGGCTGCCT[C/G]CTGCAGCCCCCATAG	57674
rs751024666	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281806	GTCCCAGATATGAAA[C/T]GGCGTGGCATTGGTA	57674
rs751034926	snp	G/T	3.47747e-05	0.00416967	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288027	AGCCACCACGCCACT[G/T]GAGGGTGACGGCCTC	57674
rs751063670	snp	A/T	1.64822e-05	0.00287068	missense	RNF213	GRCh38.p7	17:80347630	ATGGAAACAGGCAAG[A/T]TGGTGTTGCTTCTCA	57674
rs751066131	snp	C/T	3.3315e-05	0.00408122	synonymous-codon	RNF213	GRCh38.p7	17:80343247	GGATGAGAGCCGAGT[C/T]CTGGGCGCCCTGCTG	57674
rs751075803	snp	A/T	1.65141e-05	0.00287346	synonymous-codon	RNF213	GRCh38.p7	17:80298480	GGCCGCTCTGGAGGG[A/T]CTCTCCTTCTCACCG	57674
rs751079345	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358335	TCACCCCTCTGCTGG[C/T]GAGCATGATATCATT	57674
rs751085564	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387163	TCTCACTCTGTCACC[A/G]AGGCTGCAGGGCAGT	57674
rs751095306	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351816	GAGGTGAGATCAGAA[C/T]ATCAGTCAGGGTATT	57674
rs751109081	snp	G/T			intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80261402	GCGCAGCGTCCTTCC[G/T]ACTTGGCGAAGTCGC	57674
rs751112621	snp	A/G	1.64768e-05	0.00287021	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358412	CCGCCCTGGGCAAGA[A/G]ATCTTTGGATGTTTA	57674
rs751117430	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377336	TATGAAATATAGAAC[C/T]GGGAGACTGACTCAT	57674
rs751122176	snp	A/G	1.65241e-05	0.00287433	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363277	TCCACAGCCTGATGG[A/G]AGCCCGTTGGAACCA	57674
rs751134808	in-del	-/T	4.94368e-05	0.00497152	frameshift-variant	RNF213	GRCh38.p7	17:80346078	CCTCTGGTGTGGGAC[-/T]TTTGGACAACTGAGT	57674
rs751136602	snp	A/G	1.64743e-05	0.00287	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376453	AACGGTGACAGAAAT[A/G]GCCATTCATGCTGCA	57674
rs751158882	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319493	TAGTTCTCTCCGGAT[C/T]CCTCAGTGTGCTGCA	57674
rs751163431	snp	C/T	1.662e-05	0.00288266	intron-variant	RNF213	GRCh38.p7	17:80291834	GCTCAGGAGGTAAGT[C/T]GTGGCAGCAGGCTGT	57674
rs751167446	snp	A/T	3.31016e-05	0.00406813	stop-gained, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353051	TCGCGCCCGGAGACT[A/T]GCCTGAGCGTGAGTC	57674
rs751191411	snp	C/T	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345705	ACGGAGGAACAACTG[C/T]AGACATGATCTACTC	57674
rs751199091	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270327	GGCTGCATGCTTGCA[C/T]GGAGACCTTGCCCTC	57674
rs751207347	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369604	CGCTCCGCCTGAGAA[A/G]GAAGTGATTGAGAGC	57674
rs751210261	snp	A/G	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80319226	ACTGCCTACTGCAAT[A/G]GTTGCTGGGACACCA	57674
rs751213045	snp	C/G	1.67307e-05	0.00289224	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386471	GGTGCCTGCTCAGCC[C/G]AGAGTCCCTAAGCCC	57674
rs751228845	snp	A/C	0.000114175	0.00755476	missense	RNF213	GRCh38.p7	17:80336293	TATTTAAGCTGGACC[A/C]CAGCGTGGACTTCAG	57674
rs751229352	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371719	AGTATTATGCTAAAA[C/G]GTTTTCCATAAAATC	57674
rs751238748	snp	C/T	1.7235e-05	0.00293551	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383097	GTGCTGACAGCTGGG[C/T]TGCTCCTCGGTCCAG	57674
rs751249463	snp	C/T	1.69519e-05	0.0029113	intron-variant	RNF213	GRCh38.p7	17:80298553	TTATCTACATGAATC[C/T]GGGAAGACTGACTCC	57674
rs751258219	snp	A/C	1.68687e-05	0.00290414	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373120	CCTCTCCAAGCCCGG[A/C]CGCCCGCACCAGTGG	57674
rs751258272	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324053	ATCTGTGAATAGAGT[C/T]TCACTTCTTCCAATC	57674
rs751276220	snp	A/G	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80344797	CACAGAGCCTGGGAT[A/G]GATCTGTGGGAGTTC	57674
rs751284950	snp	C/T	1.64746e-05	0.00287002	stop-gained	RNF213	GRCh38.p7	17:80291761	TTCATTTACAAGCAC[C/T]AGCAGAAGAAGGGCG	57674
rs751286157	snp	A/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360545	CAGCTGGTCATTCCC[A/T]TTCTGGGCCTTCTCA	57674
rs751293597	snp	A/G	8.23839e-05	0.00641757	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379644	CCGATGGAACAGAGC[A/G]TCTGCATTGACTGCC	57674
rs751318513	snp	A/G	1.64784e-05	0.00287035	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393458	GTGTCTCAGTGTGGA[A/G]AACAGCTGCTGTGCT	57674
rs751339941	snp	C/G/T	0.000146099	0.00854584	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353494	GTGGTAACGCAATCA[C/G/T]GTTTGCTTCGACTGC	57674
rs751345072	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80291890	GCCAATCCCGCGGTA[C/G]TGGACGCGTCTCTCT	57674
rs751345254	in-del	-/GTTC	3.01555e-05	0.00388289	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372505	ATCCTTTTCTTTCTT[-/GTTC]CTTGTTCCTCAGGAT	57674
rs751346398	snp	C/T	1.6501e-05	0.00287232	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388648	AGACACGACTGGAAC[C/T]ATGAACATCTCTTTA	57674
rs751349710	snp	A/G	2.46163e-05	0.00350821	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363841	GGCGCGCGCTCACCA[A/G]GAGCCTGCCAAGTGC	57674
rs751353378	snp	A/G	6.59304e-05	0.00574116	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364449	GCCCAGTGGAGTCGG[A/G]TTTTCTCCACCGCAC	57674
rs751354962	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80294331	ACCAGGACAGTGCTC[A/C]CTTGCTAGTGGGGGG	57674
rs751357551	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394478	AGAGTCCCCGAGCCC[A/G]GATCTTGTGCTGCTT	57674
rs751371698	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80265589	AAGGATGAACTCAGG[G/T]ATTCGATGTCTGGGC	57674
rs751372260	snp	C/T	1.64914e-05	0.00287149	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375748	TCTTACTTGATACCC[C/T]TGATTTTGCAGGCCT	57674
rs751374503	in-del	-/TT	1.64741e-05	0.00286998	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375810	TTCCTGTTAACACTG[-/TT]TTTAGAGAGGTGGCT	57674
rs751376005	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370490	GATGTTACAAAAAGC[A/G]GTGATGAGTTAAACT	57674
rs751376931	snp	A/G	1.65026e-05	0.00287246	synonymous-codon	RNF213	GRCh38.p7	17:80348247	CCTTCAGGCACACCT[A/G]CACACGGCAGACCTG	57674
rs751376950	in-del	-/AAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357299	CAACAAAATATATAT[-/AAC]AACAAAATGTCTTGT	57674
rs751377131	snp	A/C	1.68134e-05	0.00289938	intron-variant	RNF213	GRCh38.p7	17:80273412	TCCAAGAAGTGAGTG[A/C]ACTGCCTCGGCTCCC	57674
rs751418512	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80303685	TCTTGTGCCTCAGCC[A/T]CCCAAGTAGCTGGGA	57674
rs751432010	snp	A/G	1.65102e-05	0.00287312	missense	RNF213	GRCh38.p7	17:80348153	TCCGGCTGAGCGCCT[A/G]CTCGCTGGGCGGGTT	57674
rs751436637	snp	C/T	1.6937e-05	0.00291002	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354183	TATGAGCCTCCCCAC[C/T]CCTCTTGCCCCTGCC	57674
rs751449660	snp	C/T	4.94287e-05	0.00497111	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361822	GCCGCAGCAGGAACT[C/T]CTTCAGTGTTACTTG	57674
rs751462487	snp	A/G	5.55602e-05	0.00527039	missense	RNF213	GRCh38.p7	17:80340072	CAGATCAGCTGAGCT[A/G]CGAGGTGGCACGCCA	57674
rs751463016	snp	C/T	1.64779e-05	0.00287031	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288747	CCTCCTTTCAAAACA[C/T]ACTGCCAGGTGCGTC	57674
rs751483069	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80333004	CTCCCAGTTCCACCC[A/C]AAAGCGGTAAATCAG	57674
rs751499459	snp	A/G	0.000114253	0.00755735	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80278778	GGGAGCTACATCAGA[A/G]GTTTTGGTAGATGCT	57674
rs751512678	snp	A/C	1.6557e-05	0.00287719	missense	RNF213	GRCh38.p7	17:80340189	ACTGCTACCTCCCCT[A/C]TGCCTTCAGCCAGCA	57674
rs751523732	snp	A/G	9.88452e-05	0.00702942	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381574	ATCATTAAGCCTCCA[A/G]TGAGGGATCCAAAAG	57674
rs751527734	snp	C/G	1.64914e-05	0.00287149	missense	RNF213	GRCh38.p7	17:80346370	AATCACACCGAGAGA[C/G]ATCCCGTCCTCTGGT	57674
rs751529205	snp	A/G	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80344898	TTCAGTATCAAGAAG[A/G]CTCTGTCGAAGGCAC	57674
rs751532714	snp	A/G	1.65146e-05	0.0028735	intron-variant	RNF213	GRCh38.p7	17:80307249	ACATGCGGCCCCCGG[A/G]GGCTTCCTCTGACCC	57674
rs751536680	snp	C/G	0.000228363	0.0106831	missense	RNF213	GRCh38.p7	17:80327967	AAAGCACAAGAATCA[C/G]TTTCTTGACATCTGG	57674
rs751543694	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375807	CTACTTCCTGTTAAC[A/G]CTGTTTAGAGAGGTG	57674
rs751556195	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80328109	GCCTTGATAATGAGT[A/T]TCTCTTCTTGCTCAT	57674
rs751558529	snp	A/G	3.29968e-05	0.00406169	missense	RNF213	GRCh38.p7	17:80290722	TCTGTGAGCTGCACT[A/G]CACCAGGTGAGCGTG	57674
rs751583951	snp	A/G	3.29571e-05	0.00405924	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385182	CTCAGGTGTGGCTCT[A/G]CTCTGACAGGACCAG	57674
rs751586146	snp	C/T	1.72293e-05	0.00293503	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389108	GGGGCTCGGCTCTCT[C/T]ACCAGGTGGTGAGAT	57674
rs751593398	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80345322	CAACATCAACGGCAG[C/T]GTCGATGCCATCAGT	57674
rs751596589	snp	C/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389931	AAGTAAGTCTGGTCT[C/G]TTCCTCTCTGCTGGA	57674
rs751623963	snp	A/G	1.80866e-05	0.00300715	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288113	CAGGAGTGGCCACAG[A/G]AAGTGAGGCTCAGAG	57674
rs751673127	snp	C/T	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80306316	GACGAGCCTCTCTTC[C/T]GGTCCTGGTTTAGTC	57674
rs751673947	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80313395	CTCGTGTCCCCTGGC[C/T]GGGCACAGTCCCTGT	57674
rs751674154	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364659	GCTCTTTTGGCTCTG[A/G]CCGTTTTGTCTAGAC	57674
rs751679411	snp	C/T	1.69859e-05	0.00291421	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288185	ACGCTTCCATCCCCT[C/T]TGGGGGCAGAGGCCT	57674
rs751683308	snp	A/G	4.94368e-05	0.00497152	missense	RNF213	GRCh38.p7	17:80346293	TCAGGTGGTTCCACG[A/G]GCACAGCGCGATGCT	57674
rs751683518	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270420	CACATTTACAATGCA[A/G]ATCTCTTCAAATCCC	57674
rs751699364	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268978	GGCTGAAGACCCGAG[A/G]TCCCCCTGGCAAACC	57674
rs751702656	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389498	GAGACAAGAACAACT[A/G]CTCACCCAGTCAGTC	57674
rs751707193	snp	C/T	1.64953e-05	0.00287182	missense	RNF213	GRCh38.p7	17:80295807	ACATCCTTGGGATAC[C/T]TCAGAGGTATTATTA	57674
rs751740826	in-del	-/AAAAAAAAAAAG			intron-variant	RNF213	GRCh38.p7	17:80268369	GAAAAAAAAAAAAAA[-/AAAAAAAAAAAG]GCAGTACTGCATCCC	57674
rs751742658	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368033	GCCCTGCGACCACGT[A/G]CACTGCCTGCGCTGC	57674
rs751752117	snp	A/G	1.6473e-05	0.00286988	stop-gained	RNF213	GRCh38.p7	17:80343874	GCAGACTGGAATTTG[A/G]GTGTTTCTTTTCAAG	57674
rs751755717	snp	G/T	3.29468e-05	0.00405861	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367955	ATTGCCCTTCTTGGA[G/T]TCTAGGTTTGGGATT	57674
rs751761786	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296428	CATCCCCTCAAGGAC[A/G]TCTGCAGAAGCAGCG	57674
rs751762156	snp	A/G	2.52223e-05	0.00355113	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373214	CACCCCCACAGCCCC[A/G]TACACCCCAAACCCA	57674
rs751774635	snp	A/T	3.29538e-05	0.00405904	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390090	CTCAGCACATTCCTA[A/T]ATCAGACTGGCCTAG	57674
rs751787395	snp	A/G	1.66885e-05	0.00288859	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376917	GCCTGAAGACTTGCT[A/G]GCTCAAGCTCGGAGG	57674
rs751789995	snp	A/G	1.64757e-05	0.00287012	synonymous-codon	RNF213	GRCh38.p7	17:80345379	AGACGTCATGACCAG[A/G]GACCTGTACCAGGGC	57674
rs751792603	snp	C/T	3.34459e-05	0.00408924	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363625	CCCTGGACGCATTTG[C/T]CGCAATGGCCTGCAC	57674
rs751812499	snp	A/G	1.65578e-05	0.00287726	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386823	ACCGTGCAGGAGTTC[A/G]ATCTGGAGAAGATTC	57674
rs751824353	snp	A/G	4.97797e-05	0.00498873	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381670	GACGAGACCATCGGC[A/G]TGGTCCACCTCGTCC	57674
rs751848030	snp	C/T	4.94458e-05	0.00497197	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374505	TAGGTACCTGGTGTA[C/T]GGCGATGAATACAAG	57674
rs751874525	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	RNF213	GRCh38.p7	17:80343979	TGAAATCCTGGAAAG[A/G]AGGACGTCAGTGCCG	57674
rs751891719	snp	A/G	3.29457e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383803	CACCTGCCCCGGAAA[A/G]GTGTGGTCCATTGCT	57674
rs751893522	snp	A/G	1.67251e-05	0.00289176	missense	RNF213	GRCh38.p7	17:80346931	CACCCGCTGCTGGAA[A/G]ACGGATGCATTGAAG	57674
rs751893613	snp	C/T	0.000167328	0.00914526	synonymous-codon	RNF213	GRCh38.p7	17:80340145	AGAAGACTACCAGCT[C/T]GTCATGGTCTGTGAT	57674
rs751900727	snp	A/G	1.65477e-05	0.00287638	missense	RNF213	GRCh38.p7	17:80346803	TCATCAGCACCTTCC[A/G]GCAGTGCGCCCGCTT	57674
rs751929420	snp	C/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320973	ACCTGGGGGACAGAG[C/G]AAGACCCTGTCTCAA	57674
rs751939207	in-del	-/AAG	1.64795e-05	0.00287045	cds-indel, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354485	CTCAGTGTCTTTTTA[-/AAG]AAGCAAGAAGAGAGC	57674
rs751952931	snp	A/G	3.29973e-05	0.00406172	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353598	GTGGCAGAGGTGGCA[A/G]AGGAGGCCATGGAAA	57674
rs751953115	in-del	-/GAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364163	GGTGAGGTGGGACTT[-/GAC]AGGCGCAGGATCATG	57674
rs751953773	snp	C/T	1.64773e-05	0.00287026	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353689	CTGGTTCTTGGGACC[C/T]CCCCTTGTGCTGCTG	57674
rs751971768	snp	A/G	1.65304e-05	0.00287488	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360063	CACCTTATTGCAGAC[A/G]TAAAGGTGAGATGGC	57674
rs751975959	snp	C/T	1.66418e-05	0.00288455	intron-variant	RNF213	GRCh38.p7	17:80263785	CCATAGCAGGTGAGG[C/T]CCAGGGGTGCTGGTG	57674
rs751976105	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387844	AGCAGGCACTTTCCC[A/C]TCTCTGTTCTTTGAC	57674
rs751994484	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359254	AATGTGCCCAGGCTC[A/G]GTGGCTCATGCCTAT	57674
rs752001455	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80278966	TGGTGCATGCTGGCA[C/T]AGCCTGGCACGGCCA	57674
rs752002286	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80348849	AGTGCTGAGATGGGG[C/T]GATGAGGTGCAGTCA	57674
rs752009490	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80272309	TAAAATAAAATAAAA[-/A]AAAGAAAAAGAAAAA	57674
rs752012522	snp	A/G/T	5.00207e-05	0.00500083	missense, stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371923	TTGACCCTGTTAAAA[A/G/T]AGAAAGCATTCATAA	57674
rs752021088	snp	C/G	1.67005e-05	0.00288963	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363669	AGAAACACCCTGAAG[C/G]CCAGTCCCCAGGCGT	57674
rs752023811	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307971	CTTGTAAATAGTCAT[A/G]ATACTGCATATGCCT	57674
rs752024169	snp	C/T	1.64773e-05	0.00287026	synonymous-codon	RNF213	GRCh38.p7	17:80306414	TCATATCCTGGACTG[C/T]CTTTCAGGGATTTAC	57674
rs752033791	snp	C/T	1.64792e-05	0.00287042	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383903	GCAAAGAAAGAGTGC[C/T]CATCCTCTGGCATTT	57674
rs752063380	snp	A/G	0.000114019	0.00754959	synonymous-codon	RNF213	GRCh38.p7	17:80339338	AATGGACTTTGGCTT[A/G]GACCTGGTGACGGAG	57674
rs752075631	snp	A/G	1.66421e-05	0.00288458	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369898	AGACTTGCTTCTGGA[A/G]AGCCCTGGCTTTTTC	57674
rs752084692	snp	C/T	1.6476e-05	0.00287014	missense	RNF213	GRCh38.p7	17:80345716	ACTGCAGACATGATC[C/T]ACTCCAGAGTCAGGG	57674
rs752088204	snp	C/G	1.64779e-05	0.00287031	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380865	CAGACCGGCCACGTG[C/G]TGGGCAACCCGCAGC	57674
rs752094262	snp	A/C	1.64738e-05	0.00286995	synonymous-codon	RNF213	GRCh38.p7	17:80345013	CCTGAATTATCAGCT[A/C]AGAGATTGTGAGGCC	57674
rs752115423	snp	C/T	1.648e-05	0.0028705	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288770	GGTGCGTCTCCTTCC[C/T]GCCTGCCGGCTCCAG	57674
rs752121486	in-del	-/C			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394954	TGTGGGGGCCGGGGG[-/C]TGGCTTGCTGAAGTC	57674
rs752123394	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288430	TGGGCTCTGCTGCAA[A/G]GTGCTGGCGTTGCTT	57674
rs752138252	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80289943	TGCCCTTCTAGTCAG[A/C]TGTTTTGGCAAGTTT	57674
rs752148300	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80261880	AAATTAGCCGGGTGT[C/G]GTGGCGCATGCCTGT	57674
rs752151337	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80330283	TTTCACTTGTTGATT[G/T]GTTTTGATTTTCCTC	57674
rs752158108	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366945	TGTATTGCCTAAAAA[C/T]CAGTGTTTCCACTTC	57674
rs752172917	in-del	-/CT			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395680	TAACTAACTTCACCC[-/CT]GAGTCCACTTGCGGG	57674
rs752176408	snp	A/G	6.59011e-05	0.00573988	missense	RNF213	GRCh38.p7	17:80345974	GGTTTGGGCTACAGG[A/G]TTAGTATGGAGGAGA	57674
rs752205553	snp	C/G	1.66874e-05	0.0028885	intron-variant	RNF213	GRCh38.p7	17:80291845	AAGTCGTGGCAGCAG[C/G]CTGTCTGCTCACCCC	57674
rs752213307	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80299789	CTCATCATTTAGCTC[C/T]CACTTACAAGTGAGA	57674
rs752220267	snp	G/T	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80294750	ATGACATAGTTTATA[G/T]GAAGCCTCATGGGAG	57674
rs752222695	snp	A/T	1.64781e-05	0.00287033	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358427	GATCTTTGGATGTTT[A/T]TTTTCAGTGACACGA	57674
rs752258666	snp	C/T	6.6346e-05	0.00575922	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379755	TAAGTACTCAAACTT[C/T]GGGGTGTTGGGCTGT	57674
rs752271884	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80306279	TCAGTTTATGAGAGA[A/G]AAGCAGCATTTGCTG	57674
rs752281369	snp	G/T			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321961	GATCTCTTGACCTCA[G/T]GATCCACATGCCTTG	57674
rs752300337	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388322	ATGAATAAATGAATG[A/G]GATATGCACAAATAC	57674
rs752312488	snp	A/G	1.64754e-05	0.00287009	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375833	AGGTGGCTATTTTGT[A/G]CAGATCCCACAATGC	57674
rs752319363	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369625	GATTGAGAGCCTGCT[C/T]TCTCTCCTCTTCGTC	57674
rs752322924	snp	A/G	6.58957e-05	0.00573964	missense	RNF213	GRCh38.p7	17:80344906	CAAGAAGGCTCTGTC[A/G]AAGGCACCCCGGAGG	57674
rs752323453	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80317023	TGGGCTGCTGTGACC[C/G]GCCACTAGCATGGCT	57674
rs752333057	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80340809	TTTTTTTGTTTTTTG[G/T]TTTTTGTTTTTTTGA	57674
rs752345628	in-del	-/ATGTT	1.64762e-05	0.00287016	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376278	CTTTGATACATCTTA[-/ATGTT]AAGTTTTTTTCCTGT	57674
rs752345854	snp	C/G	1.69618e-05	0.00291215	intron-variant	RNF213	GRCh38.p7	17:80273430	TGCCTCGGCTCCCCT[C/G]CGCCCCCGCTCACTC	57674
rs752346899	snp	G/T	0.000176392	0.00938961	intron-variant	RNF213	GRCh38.p7	17:80289616	AAAAAAAAGAAAATG[G/T]GGAGGCCGGCCTTCA	57674
rs752385599	snp	C/T	1.64784e-05	0.00287035	intron-variant	RNF213	GRCh38.p7	17:80308970	GTAACCATTTTCTGG[C/T]TTCTCCTAAATCCTT	57674
rs752385985	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80284111	ACGCCTGGAATCCCA[G/T]CACTTTGGGAGGCCG	57674
rs752400604	snp	A/G	6.66678e-05	0.00577317	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353561	GGAGGCGATGGAGAC[A/G]GAGGCCAGCACATCA	57674
rs752403171	snp	A/G	1.64757e-05	0.00287012	intron-variant, missense	RNF213	GRCh38.p7	17:80319334	AATCTCTCCTCCTGG[A/G]AAACGGATTCGGGCT	57674
rs752404878	snp	A/G	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393466	GTGTGGAAAACAGCT[A/G]CTGTGCTGAAATGGA	57674
rs752406629	snp	A/G	1.64765e-05	0.00287019	missense	RNF213	GRCh38.p7	17:80344819	TGGGAGTTCTGCAGC[A/G]AAACTTTCCAAAGAC	57674
rs752407315	snp	A/T	1.65154e-05	0.00287358	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364402	TTGGTGGGAGCCGAG[A/T]GAGTGAGTGAGTGGC	57674
rs752427994	snp	C/T	4.94621e-05	0.00497279	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354445	CCTTTGTACAGCCTC[C/T]TTCTTGCGGGTATCC	57674
rs752436489	snp	A/T	1.64795e-05	0.00287045	intron-variant	RNF213	GRCh38.p7	17:80349722	GGCAGCAGACTTGCA[A/T]CCTTTCCTTGAAGTC	57674
rs752442204	snp	A/G	1.69072e-05	0.00290746	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389116	GCTCTCTTACCAGGT[A/G]GTGAGATGCCAGAAA	57674
rs752446568	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391738	TACTAGGATCTTCCT[C/T]ATCCCAGGATTATAA	57674
rs752447524	snp	A/G	1.64749e-05	0.00287005	missense	RNF213	GRCh38.p7	17:80344951	TTCCTGTTTCACTGC[A/G]GGGTAATAAACCCAT	57674
rs752449152	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359763	CAAGTTATCAAAGCC[A/T]GACAGGTTCAGGAAC	57674
rs752459248	snp	C/T	1.64838e-05	0.00287083	missense	RNF213	GRCh38.p7	17:80345786	AGTTGGACACCATCT[C/T]GTTTTTTGATGAAGC	57674
rs752475961	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80294163	GGTCTGCACTCATAT[C/G]GTTTGCAATGGAGCC	57674
rs752476939	snp	A/C	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80309032	GGATTCCCGAGGAGG[A/C]CTTGTCACCATCCTA	57674
rs752479961	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351941	CTCACTACAACCTCA[A/G]TCTCCTGGGTTCAAG	57674
rs752481085	snp	A/T	1.64757e-05	0.00287012	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361849	CTTGAAGGATTTCAT[A/T]CTCTTGACCATGCGT	57674
rs752486685	snp	C/T	1.65523e-05	0.00287678	missense	RNF213	GRCh38.p7	17:80347361	CCGAGGCCAAGTGCT[C/T]AGAGGAAGTCAGCCC	57674
rs752488073	snp	C/T	4.94181e-05	0.00497057	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389232	GCAGTCCTACAGCGA[C/T]GCCTGTGAAGTGCTG	57674
rs752489326	in-del	-/TGCT	1.6674e-05	0.00288734	intron-variant	RNF213	GRCh38.p7	17:80263792	GGTGAGGCCCAGGGG[-/TGCT]TGCTGGTGGAGGCTG	57674
rs752513500	in-del	-/CAGA	1.6492e-05	0.00287154	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380839	TTTCCAGAGACAAGG[-/CAGA]CAGAACGCAGACCGG	57674
rs752518982	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355572	TTATGGAGGAAGAAG[C/T]GGGGTGAGTGGGAAT	57674
rs752527941	snp	C/T	1.71346e-05	0.00292694	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287805	AGTGAGTGTCTCTCT[C/T]TCTGTTTAGAGCAAA	57674
rs752530621	snp	A/G	3.30311e-05	0.0040638	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361926	AGGGTCAGGTGTAGA[A/G]CTTGCATGATGGGGA	57674
rs752545753	snp	C/T	3.30366e-05	0.00406413	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375886	GTGAGTAACCGCCTG[C/T]AGGGCTGTGTTCAAA	57674
rs752548047	snp	C/G	0.000570483	0.0168795	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80278811	TGTAGACCTCATATC[C/G]GATGAATGGGAAGCT	57674
rs752562024	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292759	CTGGACTCCCAGTGC[C/T]GCCTCCTCACCTGGG	57674
rs752563843	snp	C/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395414	GTCCTTTAGAAGCAC[C/G]CATGAAGTAGTGTGT	57674
rs752572099	snp	C/G	1.67223e-05	0.00289151	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351692	TTAAATAGGTATTCT[C/G]TTATAAATGAAATCA	57674
rs752573417	snp	A/G	0.00011411	0.0075526	missense	RNF213	GRCh38.p7	17:80334130	TCGACGACTTTCGCC[A/G]TGAAACACTGGACCA	57674
rs752575093	snp	C/G	0.000231378	0.0107534	intron-variant	RNF213	GRCh38.p7	17:80313204	TCTGGGTAGGGATGT[C/G]ACTGATCGTGATTCC	57674
rs752578610	snp	A/G	2.09699e-05	0.00323798	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372962	CTCACCCGCTTTCTC[A/G]TTGGCCTCTCAGAGA	57674
rs752579947	snp	A/G	1.65135e-05	0.00287341	missense	RNF213	GRCh38.p7	17:80295695	CTTTTTGTAGTGGAA[A/G]AAATTGAGCTTTTAT	57674
rs752591351	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80324316	CATAGAAGAGAGTTG[G/T]ATTTTGTCAAATGCT	57674
rs752591456	snp	C/T	0.000119567	0.00773106	synonymous-codon	RNF213	GRCh38.p7	17:80332064	CAGTAAAAGATTAAA[C/T]GACACCGTGACAGTG	57674
rs752601631	snp	C/T	1.65542e-05	0.00287695	intron-variant	RNF213	GRCh38.p7	17:80295820	ACCTCAGAGGTATTA[C/T]TATTTTTTGTCAAAA	57674
rs752629050	snp	A/G	4.94271e-05	0.00497102	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368044	ACGTGCACTGCCTGC[A/G]CTGCCTCAGGGCCTG	57674
rs752657780	snp	A/T	0.000131893	0.00811969	missense	RNF213	GRCh38.p7	17:80345416	CTCCAGAGGGTGCCC[A/T]TCAATGTCGACTTTG	57674
rs752662991	snp	A/G	6.59076e-05	0.00574016	synonymous-codon	RNF213	GRCh38.p7	17:80345991	TAGTATGGAGGAGAC[A/G]GCCGACAGGCTGGGC	57674
rs752669448	snp	A/G	4.94507e-05	0.00497221	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390106	ATCAGACTGGCCTAG[A/G]CGCCTTCCTGCTAGA	57674
rs752724887	snp	A/G	5.29367e-05	0.00514447	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385652	CCTGTACCACTAAGC[A/G]TTCCAGGAGAGCCTC	57674
rs752730501	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391075	TCAAAAACAAACAAA[A/C]AAAAGAATAGAAAAA	57674
rs752747357	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393993	TGATGTGAAAAACTA[C/T]CAGACTGTTTTTTGT	57674
rs752750161	snp	A/G	3.41262e-05	0.00413061	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288279	TGCCCAGGAGCTCCT[A/G]TTGCCTGAGTCAAAA	57674
rs752750278	snp	A/C	1.65096e-05	0.00287306	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352906	CAGCCGGGAAAGACA[A/C]AAAGACAGTTGTGGG	57674
rs752752383	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382466	TCAGGTACTTCTTTG[A/C]CTGAAACTGGCATTC	57674
rs752752436	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365387	GAGCAGCCCAAGGCT[-/A]AAGGTACCAGCTCCC	57674
rs752752683	snp	C/T	1.64939e-05	0.0028717	missense	RNF213	GRCh38.p7	17:80346386	ATCCCGTCCTCTGGT[C/T]GTTGATGCTGGCCAT	57674
rs752764790	snp	A/T	1.67553e-05	0.00289437	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376933	GCTCAAGCTCGGAGG[A/T]GGAAGGGTCTGGAGC	57674
rs752778643	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390035	TGGGGAAATCAGTTC[A/G]AGGTACAAAGCGGAT	57674
rs752784235	snp	C/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80343890	GTGTTTCTTTTCAAG[C/G]TCCTCATTTTACAAT	57674
rs752787130	snp	C/T	1.64904e-05	0.00287139	synonymous-codon	RNF213	GRCh38.p7	17:80345526	GTATGAGCTCACAAC[C/T]GACAATATGCTTAAA	57674
rs752796426	snp	C/G	6.66928e-05	0.00577425	intron-variant	RNF213	GRCh38.p7	17:80263792	AGGTGAGGCCCAGGG[C/G]TGCTGGTGGAGGCTG	57674
rs752808343	in-del	-/C	1.6691e-05	0.00288881	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363668	AGAAACACCCTGAAG[-/C]CCCAGTCCCCAGGCG	57674
rs752820465	snp	A/T	1.6633e-05	0.00288378	intron-variant	RNF213	GRCh38.p7	17:80273220	TCTGAGATCTGACCC[A/T]TCCTTCATCTGCCGT	57674
rs752840165	snp	A/G/T	8.48639e-05	0.00651353	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288197	CCTCTGGGGGCAGAG[A/G/T]CCTGTCCCAGGAGGG	57674
rs752840207	snp	C/T	1.64751e-05	0.00287007	intron-variant	RNF213	GRCh38.p7	17:80291617	GCCAACCGTATCCTG[C/T]TCATTCACAGAGACT	57674
rs752840885	snp	A/T	1.66827e-05	0.00288809	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369916	CCCTGGCTTTTTCTC[A/T]TCATCGCAGCGTTTT	57674
rs752860337	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80329876	GGGTATTAATAGGTA[-/G]GGTCTTTCAACTCTA	57674
rs752872098	snp	A/C	1.84725e-05	0.00303906	missense	RNF213	GRCh38.p7	17:80317209	AGGCGGCTGGTGGAA[A/C]TCCAATTCCCCGCGG	57674
rs752875482	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80272055	TTTGAGAGGGCAAGA[C/T]GGGTGGATCATGAGG	57674
rs752875980	snp	A/G	1.64795e-05	0.00287045	synonymous-codon	RNF213	GRCh38.p7	17:80343991	AAGGAGGACGTCAGT[A/G]CCGTCGAGGAGCTCT	57674
rs752883030	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365561	GCCCAATCCCGGACA[C/T]GCACACGCCACACCA	57674
rs752887733	in-del	-/GGT	1.65408e-05	0.00287578	splice-donor-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354576	AGGCGGGCACATTCA[-/GGT]ACTGTGACTAAAGGA	57674
rs752892188	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286104	CTGTCCACACCCAAA[C/T]GCACCAAGTGTGCCA	57674
rs752898172	snp	A/G	1.82984e-05	0.00302471	missense	RNF213	GRCh38.p7	17:80317257	TCGTTGCTGGGAGAC[A/G]TGGAATGGAGGCTCA	57674
rs752899431	snp	A/C	1.64882e-05	0.00287121	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383923	CTCTGGCATTTCCTG[A/C]AGAAGGTATGTCTGG	57674
rs752904255	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388117	TACAGGCGCCCGCCA[C/T]CATGCCCGGCTAATT	57674
rs752904494	snp	C/T	1.67725e-05	0.00289585	missense	RNF213	GRCh38.p7	17:80346941	TGGAAGACGGATGCA[C/T]TGAAGACGATCCCGC	57674
rs752907164	in-del	-/TTA			intron-variant	RNF213	GRCh38.p7	17:80282405	TTTTATTTATTATTG[-/TTA]TTATTTTTTGAGATG	57674
rs752910151	snp	A/G	5.22116e-05	0.00510912	intron-variant	RNF213	GRCh38.p7	17:80306486	TTGTGTCTGAAGTCG[A/G]CTCTGGAGTCCTGGC	57674
rs752912234	snp	A/C	0.000280985	0.0118496	missense	RNF213	GRCh38.p7	17:80294940	TTGCTTTGTCCTGCA[A/C]CAGCCTATGATTTAT	57674
rs752913580	snp	C/T	4.38625e-05	0.00468288	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386886	AAGCCCCGGCTGAGC[C/T]TCAAGGTAGGGCTGA	57674
rs752976704	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364908	CCATCTGTGGAAGCT[A/G]TTACCATTTTCATAG	57674
rs752977283	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328238	TCCTTCTCCTGGTGG[C/T]GGGGAAGGTGCGGCG	57674
rs752982011	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80296567	TGGTACCTGCTCAGA[A/C]CCCACTGAGCTCTGC	57674
rs753003842	snp	G/T	1.648e-05	0.0028705	synonymous-codon	RNF213	GRCh38.p7	17:80306423	GGACTGTCTTTCAGG[G/T]ATTTACTACCGGCTT	57674
rs753005354	snp	A/G	1.65048e-05	0.00287265	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385020	AAAAATTGTTACTGG[A/G]TGGTCTTCCCTTCTC	57674
rs753019189	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377033	AGATGCTATGAAGCA[C/T]TGGGTTCGACTTGGG	57674
rs753033886	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380873	CCACGTGCTGGGCAA[C/T]CCGCAGCGGAGAGAC	57674
rs753043738	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	RNF213	GRCh38.p7	17:80346093	CTTTGGACAACTGAG[C/T]GACGTTGCTGAAAAG	57674
rs753044530	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80305688	GTGATCTCGGCTCAC[G/T]GCAATCTCTGCCGCC	57674
rs753058029	snp	A/G	0.000114659	0.00757076	missense	RNF213	GRCh38.p7	17:80339723	ATCATGGAGCAGTCC[A/G]TGAGGTGCCTTCCTG	57674
rs753062940	in-del	-/G	2.41779e-05	0.00347684	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386895	CTGAGCCTCAAGGTA[-/G]GGCTGACTCCTGCCA	57674
rs753072619	snp	A/G	2.36824e-05	0.00344102	missense	RNF213	GRCh38.p7	17:80289836	CAGGAAGTGAAGGCA[A/G]GGTAGGGATGCCCCC	57674
rs753076389	snp	A/G	3.29538e-05	0.00405904	missense	RNF213	GRCh38.p7	17:80349881	CAGCAGTTTGACACC[A/G]AGTACTCATTCCTCA	57674
rs753079463	snp	C/T	1.66624e-05	0.00288633	stop-gained, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354061	CTGAGAAGCTGTGTG[C/T]AGAGCGCCGTGGGCA	57674
rs753096389	snp	A/C	1.64743e-05	0.00287	intron-variant	RNF213	GRCh38.p7	17:80290527	CACATGGCAGGTGGA[A/C]AGATCTCACGGGAAT	57674
rs753107817	snp	C/G	1.65682e-05	0.00287817	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319487	GAAATCTAGTTCTCT[C/G]CGGATTCCTCAGTGT	57674
rs753131583	snp	C/T	1.66724e-05	0.0028872	missense	RNF213	GRCh38.p7	17:80347039	GGCATTTTTGTGTCA[C/T]GTGGCAGCCCCAACG	57674
rs753136889	snp	C/T	1.648e-05	0.0028705	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353711	GTGCTGCTGGTGATG[C/T]TTCTGAGCTGCATCT	57674
rs753137220	snp	A/G	1.64963e-05	0.00287192	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386331	TCTTGCCACGCCGAC[A/G]GGGCCTGGGCCTCTG	57674
rs753144201	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80282000	CAGCTGGGACTATAG[G/T]CGCCTGCCACCACAC	57674
rs753181825	snp	A/G	1.74671e-05	0.00295521	intron-variant	RNF213	GRCh38.p7	17:80295038	CTGCTCTACCTGCTG[A/G]GCAGGAGCCACACCT	57674
rs753192598	snp	A/C/T	3.50227e-05	0.00418454	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389380	AAGGTGGGTCTCACA[A/C/T]CGAAAAGGAAATCAG	57674
rs753193368	snp	C/T	1.66158e-05	0.0028823	intron-variant	RNF213	GRCh38.p7	17:80312969	GCCGGGAACCTGAGT[C/T]CACAGCCGAGGATGA	57674
rs753195017	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269279	ACAATACTTTACCAA[C/T]TACCTAGGCATCCTT	57674
rs753195058	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80263487	GGGGGCAGCACAGAG[C/T]GGGGAGGGGCTGGGC	57674
rs753199164	snp	A/C	5.99646e-05	0.00547528	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287966	TGCCCCACAGCCAAG[A/C]CCAGCAGAGTGGCCC	57674
rs753203087	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388524	GGCACTACGCTGCAG[-/T]TTTTCCGGCTGCAGA	57674
rs753204649	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80314461	TAATGGAGGTGATGG[C/T]GGTGATGGTGATGGT	57674
rs753208141	snp	C/T	0.000228206	0.0106795	missense	RNF213	GRCh38.p7	17:80325091	AATTTGGCATCGTCT[C/T]GTCTGCTGTGATCAC	57674
rs753218113	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80322008	GGATTACAGGCGTGA[A/G]CCACTGTGCCCGGCC	57674
rs753218197	snp	C/G			missense	RNF213	GRCh38.p7	17:80309143	CTGCCGAGATTGTCT[C/G]CAGAATGATTAGACT	57674
rs753219278	snp	C/T	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80344916	CTGTCGAAGGCACCC[C/T]GGAGGAATGCCTCCA	57674
rs753235888	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349677	TGCACCGCGCTGAAC[A/G]TCGCAGGTTTCTAGG	57674
rs753242068	snp	C/G	3.2987e-05	0.00406108	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389800	GTGAGACCTCAGCCC[C/G]CACTCAGGAATTCTA	57674
rs753270179	snp	G/T	0.00011462	0.00756946	intron-variant, missense	RNF213	GRCh38.p7	17:80278888	TTGAGGCCGCCAGCG[G/T]GCCTTCTGCAGACTG	57674
rs753272240	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80278985	CTGGCACGGCCACCT[C/T]GCACTTCCGGCCCTT	57674
rs753276692	snp	A/T	3.29516e-05	0.00405891	intron-variant	RNF213	GRCh38.p7	17:80309185	TGGTAAGTGGAGTCA[A/T]CACACAAGGTATCAC	57674
rs753292381	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394361	GTCTCAGTGTGCTCT[C/T]GCATGTATGAATATC	57674
rs753306133	snp	C/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321070	CCAAAATGCTTGAGA[C/G]CAGAAGTGTTTTGGA	57674
rs753314456	snp	C/G/T	8.2364e-05	0.00641686	missense	RNF213	GRCh38.p7	17:80345156	CCTCTGACCAAAGCC[C/G/T]GGGGAAGCACATGGT	57674
rs753322026	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	RNF213	GRCh38.p7	17:80345955	CTGCCGTTTGGAGTC[A/G]GCTGGTTTGGGCTAC	57674
rs753324772	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379351	GGAAGGTTGAATTTT[-/A]TATATTTGTCTATAA	57674
rs753327234	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80275919	CACCCGCCTCGGCCT[C/T]CCAGAATGTTGGGAT	57674
rs753340878	snp	A/G	1.67175e-05	0.0028911	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379766	ACTTTGGGGTGTTGG[A/G]CTGTTTTTATTCCAG	57674
rs753351093	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259947	CAGGATGAGGGTCCC[C/T]TCTGGAATGCGCAGA	57674
rs753352325	snp	C/T	0.000115174	0.00758774	missense	RNF213	GRCh38.p7	17:80332293	TCAGAAAGGCACATC[C/T]TTGAGCTTGAAGAGG	57674
rs753361599	snp	A/G	1.64866e-05	0.00287106	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393485	TGCTGAAATGGAATC[A/G]AGAAATGAGATAGAA	57674
rs753376013	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369232	GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA	57674
rs753413070	snp	C/T	1.68692e-05	0.00290419	intron-variant	RNF213	GRCh38.p7	17:80289623	AGAAAATGTGGAGGC[C/T]GGCCTTCAAGGTCAG	57674
rs753429637	snp	C/T	1.64741e-05	0.00286998	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385664	AGCGTTCCAGGAGAG[C/T]CTCGTCTGAAAGCTC	57674
rs753445044	snp	C/T	1.64909e-05	0.00287144	intron-variant, missense	RNF213	GRCh38.p7	17:80319404	AGCACCCGCTGGGTC[C/T]CAGCTCCTCCGCTAA	57674
rs753453931	snp	G/T	1.74964e-05	0.00295769	synonymous-codon	RNF213	GRCh38.p7	17:80340325	TGACCGGCTGTGTGT[G/T]GGGATCGTGGCCTCG	57674
rs753463982	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380665	CGGAAAGGCGAGTCT[A/G]TCATGAGAGAGACTC	57674
rs753467321	in-del	-/C	1.6478e-05	0.00287032	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381537	CACTCTGTTCCGTTG[-/C]CCCCCACAGGCTCTG	57674
rs753469899	snp	C/T	1.81909e-05	0.00301581	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372759	CTCTGCCTTGCTTTC[C/T]TTTGGGTTTAAAGAC	57674
rs753471278	snp	C/T	1.67097e-05	0.00289043	intron-variant	RNF213	GRCh38.p7	17:80295841	TTTGTCAAAATGTTT[C/T]TTATAGCTATTATAA	57674
rs753471817	snp	C/T	2.09897e-05	0.0032395	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363075	TGTAATTTAAAAATA[C/T]ATTCTAAAAGCTTTT	57674
rs753473062	in-del	-/TTT			intron-variant	RNF213	GRCh38.p7	17:80322161	CCCCCCCACCCCCCC[-/TTT]TTTTTTTTTTTTTTT	57674
rs753473462	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80290170	GGCCACCTCTTCTTC[C/G]TCCATTTTGGAGGCA	57674
rs753481703	in-del	-/CCTT	1.66324e-05	0.00288374	intron-variant	RNF213	GRCh38.p7	17:80273218	TCTCTGAGATCTGAC[-/CCTT]CCTTCATCTGCCGTT	57674
rs753481856	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	RNF213	GRCh38.p7	17:80309138	CTTATCTGCCGAGAT[C/T]GTCTGCAGAATGATT	57674
rs753483222	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80277787	TATGCGTGAACGGTG[C/G]TCTAAGCGCAGACGC	57674
rs753485812	in-del	-/CCCTGTA	1.71622e-05	0.0029293	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385636	GGTTAGTATCCTGTC[-/CCCTGTA]CCACTAAGCGTTCCA	57674
rs753493557	snp	A/G	2.18553e-05	0.00330563	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287843	AAAGGAAGAAGAAAA[A/G]GAAGGGGAACAAGTC	57674
rs753519874	snp	A/G	1.76269e-05	0.00296869	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381714	CCAAGAGCAGCACCA[A/G]CTCTCTAGCAGAAGT	57674
rs753541791	snp	C/G	1.6473e-05	0.00286988	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389237	CCTACAGCGATGCCT[C/G]TGAAGTGCTGTCTGT	57674
rs753542031	snp	C/T	1.64874e-05	0.00287113	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351811	CCACGGAGGTGAGAT[C/T]AGAACATCAGTCAGG	57674
rs753546396	snp	A/G	4.94214e-05	0.00497074	splice-acceptor-variant	RNF213	GRCh38.p7	17:80291626	ATCCTGTTCATTCAC[A/G]GAGACTTGGGTCATG	57674
rs753559980	snp	A/G	1.65943e-05	0.00288043	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375908	GTGTTCAAAGTCTCA[A/G]TATTTGGAGGGATTT	57674
rs753565812	snp	C/T	0.000148364	0.00861163	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380855	AGACAGAACGCAGAC[C/T]GGCCACGTGCTGGGC	57674
rs753572240	snp	A/G	8.26658e-05	0.00642854	missense	RNF213	GRCh38.p7	17:80347372	TGCTCAGAGGAAGTC[A/G]GCCCCATGCAGCTGA	57674
rs753577079	snp	C/T	3.49296e-05	0.00417895	intron-variant	RNF213	GRCh38.p7	17:80343087	TGCTAGGATTACAGG[C/T]GTGAGCCACCACTCC	57674
rs753580512	snp	A/G	4.94205e-05	0.0049707	missense	RNF213	GRCh38.p7	17:80344982	CCTGGTCAGAGCTTC[A/G]GAACTTTGCTCGGTT	57674
rs753589754	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374135	GCACTGTTTGACTAC[C/T]ACCTGGGGTTTAGAG	57674
rs753603739	snp	C/T	1.64895e-05	0.00287132	missense	RNF213	GRCh38.p7	17:80347487	CCAAAAACTACGTGG[C/T]ACTGCAGATCCTGCA	57674
rs753613127	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80342260	TCTGCAGGCACACTC[C/T]GATGTTCACAGTGAC	57674
rs753621678	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80272257	CCTCTGCACTCCAGC[C/T]TGGGCGACAGAGCAA	57674
rs753643941	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80311940	GAGACCAGCCTGGCC[A/T]ACATGGTGAAACCCT	57674
rs753645827	snp	A/T	1.78618e-05	0.00298841	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372984	TCTCAGAGATGGCCA[A/T]GGAGAAGCAGTGCTA	57674
rs753654353	snp	A/C/G	0.000186202	0.0096471	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355323	GAAGAAGCGGGGTGA[A/C/G]CGGTAATGGGGGCTT	57674
rs753695705	snp	C/T	1.64936e-05	0.00287168	missense	RNF213	GRCh38.p7	17:80346389	CCGTCCTCTGGTCGT[C/T]GATGCTGGCCATCGG	57674
rs753701491	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396221	GAGCTATGATTGCAC[C/G]ACTGCACTCCAACCT	57674
rs753707535	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352681	AGGCCTTATCCATGC[A/G]TCCTTCCCACGCTGG	57674
rs753707562	snp	A/G	1.65482e-05	0.00287643	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354579	CGGGCACATTCAGGT[A/G]CTGTGACTAAAGGAA	57674
rs753707787	snp	A/G	1.65029e-05	0.00287248	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363147	AGGAAACTGAAAGCG[A/G]CGTCAGAAGCGCCCG	57674
rs753727011	snp	A/C	1.70901e-05	0.00292314	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288291	CCTGTTGCCTGAGTC[A/C]AAAGGAGGCAGCTCT	57674
rs753731394	snp	A/G	1.68128e-05	0.00289933	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363701	GCTACAGTTGGTGAA[A/G]AATCTTTCCATGCCG	57674
rs753743898	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80294351	CTAGTGGGGGGATGC[A/G]GTTTCTGTATGACAC	57674
rs753795894	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362610	CGGCTGACAGTGTAG[C/T]GTGCACAGTGGGCGC	57674
rs753795997	snp	A/G	2.03917e-05	0.00319303	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377008	CTCCTTTGAGCTTCA[A/G]AGGGTGTCCAGATGC	57674
rs753804332	snp	A/G	4.94238e-05	0.00497086	missense	RNF213	GRCh38.p7	17:80345590	ATCCCGGTTATCATC[A/G]TGGGAGAAACTGGCT	57674
rs753830081	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307527	CCCACCACGCCCAGC[C/T]AATTTTTGTGTGTTG	57674
rs753842819	snp	C/T	8.25662e-05	0.00642466	synonymous-codon	RNF213	GRCh38.p7	17:80348133	CGCTACGCCCGATGC[C/T]GTGGTCCGGCTGAGC	57674
rs753846164	snp	C/T	1.7303e-05	0.00294129	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382943	GCTGTGTTCTTTGTG[C/T]CTTGGGTAACCTACA	57674
rs753856975	snp	A/G	1.993e-05	0.00315668	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360200	CAGTACATCACAGAC[A/G]CAGAAGGTGAGGCTA	57674
rs753865026	snp	A/C/T	0.000118259	0.00768875	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383637	CTGTTTGTAGCAATA[A/C/T]CTCACTTCCAGAATT	57674
rs753870192	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80335494	TCAGTGAGTAATTTA[C/T]CTGAGGGGAATGATC	57674
rs753895832	in-del	-/TCC			intron-variant	RNF213	GRCh38.p7	17:80269521	CTATCTATCCATCCA[-/TCC]TCTTTCTATTCATCC	57674
rs753901063	snp	A/G	1.66394e-05	0.00288434	synonymous-codon	RNF213	GRCh38.p7	17:80273287	GGCCTCGGAGGGTGA[A/G]ATGGAGTGTGGGCAG	57674
rs753923228	snp	A/G	3.32635e-05	0.00407807	intron-variant	RNF213	GRCh38.p7	17:80273227	TCTGACCCTTCCTTC[A/G]TCTGCCGTTACAGAT	57674
rs753924460	in-del	-/AAAG	1.6699e-05	0.0028895	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371922	TTTGACCCTGTTAAA[-/AAAG]AAAGCATTCATAACT	57674
rs753926725	snp	A/T	1.64814e-05	0.00287061	intron-variant	RNF213	GRCh38.p7	17:80344632	CACAAAAGCATTTCT[A/T]AGAAAGTCTTCTTGT	57674
rs753952938	snp	C/T	4.95913e-05	0.00497928	missense	RNF213	GRCh38.p7	17:80348053	GAGAGGCAGGGTCCC[C/T]GGGCCTTGACGGAGG	57674
rs753964368	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80267087	CTGGGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA	57674
rs753987450	in-del	-/AAT			intron-variant	RNF213	GRCh38.p7	17:80304657	ATAAATAAATAAATA[-/AAT]AATAATAATAATAAT	57674
rs753992064	snp	C/T	1.64879e-05	0.00287118	intron-variant	RNF213	GRCh38.p7	17:80307081	GCAATGACAGTGGCA[C/T]TGTGATTCAATCTTT	57674
rs753994521	snp	A/G	1.6534e-05	0.00287519	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360091	GGCCTACATCGTGGT[A/G]CAGAACCACATGAAC	57674
rs754009032	snp	C/T	3.30759e-05	0.00406655	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371965	ACTGAACTGTACATG[C/T]TCTTCATCAACTGCC	57674
rs754028056	snp	A/G	1.96899e-05	0.0031376	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374623	TTCTCTCTGATACCA[A/G]GTGGCATCCCTTGGA	57674
rs754029982	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377771	TCACAGCTTGTCCCA[A/G]CGGCCATCCTTGCTC	57674
rs754039360	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382735	TTCAGTAATTTTTTT[C/G]AAAATGGGTCTAAGA	57674
rs754041935	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80276345	CTTCAGGTGCTCTGC[A/C]CACCTCAGCCTCCCA	57674
rs754046368	snp	A/G	3.31967e-05	0.00407397	synonymous-codon	RNF213	GRCh38.p7	17:80295589	GCAACATCTGAAAAA[A/G]CACGTGGTACCATTG	57674
rs754048793	snp	C/T	3.29935e-05	0.00406149	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380953	GGCTACTCACTCACT[C/T]GGCTCTGCTTCTGGG	57674
rs754054671	snp	C/T	2.62072e-05	0.00361979	intron-variant	RNF213	GRCh38.p7	17:80289850	AAGGTAGGGATGCCC[C/T]CGCAGGGGAGCAAAG	57674
rs754058658	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265798	ACTTAAGCCGGATGC[C/T]GTGGTTCACACCTAC	57674
rs754067611	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384077	AGCAGAAGACTCAGG[G/T]CTAGAGATCTTCATA	57674
rs754084210	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357600	TTTTCCAAATGAATC[G/T]TCATAATTTTATTTA	57674
rs754092717	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356415	ACTAGGCCTGGCTCC[A/G]TCGTGTTCTGTGGTC	57674
rs754100273	snp	C/T	4.94425e-05	0.0049718	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385035	GTGGTCTTCCCTTCT[C/T]CAGGAAGCAGAGCTG	57674
rs754104139	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391149	GATATTATCCATCTT[G/T]TACATAGTTGCCAAT	57674
rs754128760	snp	C/T	1.64781e-05	0.00287033	synonymous-codon	RNF213	GRCh38.p7	17:80346102	ACTGAGTGACGTTGC[C/T]GAAAAGCTCTACATC	57674
rs754136679	snp	C/G	1.65833e-05	0.00287948	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381025	AATGGGCTCAGTTAA[C/G]AACCTGCTTTCGCTT	57674
rs754138420	in-del	-/C			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321839	CAAGCAATTCTCCTG[-/C]CTCAGTCTCTCGAGT	57674
rs754162143	snp	A/G	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80345219	CGCCCTTCTCCCTCC[A/G]GAAGAGGTGGGAGTC	57674
rs754169951	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366350	GGCTGCAGCATCTTT[C/T]TTACATCCCCACCAG	57674
rs754185085	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365609	CTAAACTTAGGCACT[C/T]GGCCTTATCTGGTTG	57674
rs754185720	snp	C/G	0.000132301	0.00813223	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363287	GATGGAAGCCCGTTG[C/G]AACCATGAGCTGGCT	57674
rs754198243	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284596	AATGGAAAGCCCAGC[C/T]CCACCTTTCTAATCC	57674
rs754203985	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328986	ACTGCGTTAATGATA[C/T]GCTGTTTTCATTGTA	57674
rs754207552	snp	A/G/T	0.000120504	0.00776127	synonymous-codon	RNF213	GRCh38.p7	17:80339995	TGAGGAGGTGGCACT[A/G/T]TTGCTGCGCCGCTGC	57674
rs754216312	snp	A/G	3.29685e-05	0.00405995	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389815	CCACTCAGGAATTCT[A/G]TTCCTTCTGCAGGCC	57674
rs754220681	snp	C/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80346176	AAAACGGGACTCGCG[C/T]GATCACAGAAGTCCT	57674
rs754244690	snp	C/G	1.64808e-05	0.00287057	missense	RNF213	GRCh38.p7	17:80347667	AGAACCTCTACGAGA[C/G]CCTCTACGACGCACT	57674
rs754253665	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265799	CTTAAGCCGGATGCC[A/G]TGGTTCACACCTACA	57674
rs754259945	snp	A/C/G	8.37309e-05	0.00646988	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354166	GATGACGCGTGCCAC[A/C/G]GTATGAGCCTCCCCA	57674
rs754273917	snp	A/G	1.64768e-05	0.00287021	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358343	CTGCTGGCGAGCATG[A/G]TATCATTCATCGACA	57674
rs754273941	snp	A/C	1.71525e-05	0.00292847	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363568	TGGTGGGCCGGTGGG[A/C]GGGGCACCGCTCAGC	57674
rs754275571	snp	C/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319862	CCCTGCTCACATTTC[C/G]TAATTGGACACTTAA	57674
rs754276887	snp	A/G	5.0647e-05	0.00503199	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373122	TCTCCAAGCCCGGCC[A/G]CCCGCACCAGTGGGT	57674
rs754282946	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351561	GGAACGGGTGGCCGT[A/G]AGACCGAACCAACAG	57674
rs754283425	snp	A/T	5.65339e-05	0.00531637	intron-variant	RNF213	GRCh38.p7	17:80350254	AATTTTCTTTTCCAT[A/T]TTTTTAAGACAGAGA	57674
rs754286071	snp	A/G	4.9489e-05	0.00497414	intron-variant	RNF213	GRCh38.p7	17:80306204	CCTCCATTTTCCCTC[A/G]CTGATCTCACTGCGT	57674
rs754288362	in-del	-/T	1.6522e-05	0.00287414	frameshift-variant	RNF213	GRCh38.p7	17:80346843	AAGGACCTGCAGCAG[-/T]TACGTCTCTGTGGTG	57674
rs754320594	snp	A/G	4.9423e-05	0.00497082	intron-variant	RNF213	GRCh38.p7	17:80290537	GTGGACAGATCTCAC[A/G]GGAATCAGATTTCTG	57674
rs754353714	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311925	AGAGGTTAGGAGTTC[A/G]AGACCAGCCTGGCCA	57674
rs754357430	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80296848	CACCACTTCCAGCTA[A/C]TTTTTGTATTTATTG	57674
rs754358908	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RNF213	GRCh38.p7	17:80345289	AACCATGACATTCAT[C/T]GGCTTCCATCTGCAG	57674
rs754376124	in-del	-/T	1.76101e-05	0.00296728	intron-variant	RNF213	GRCh38.p7	17:80350411	AGTATGTTTTTAGTA[-/T]TTTTCTCAGAAACTA	57674
rs754396070	snp	C/T	1.65466e-05	0.00287628	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386645	ATAGAGCCCTAGGCC[C/T]GCATGCCTGGCCTGG	57674
rs754411748	snp	C/T	1.74488e-05	0.00295366	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383105	AGCTGGGTTGCTCCT[C/T]GGTCCAGAAAGGAAG	57674
rs754416026	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378454	GTGGTAGTTAGTTAT[G/T]AGTATTACTTACTTG	57674
rs754418052	snp	A/C	3.34409e-05	0.00408893	missense	RNF213	GRCh38.p7	17:80346659	AGCCCGGCAGCTCCA[A/C]GTCTCTCGCCAAGAC	57674
rs754425655	snp	G/T	1.68587e-05	0.00290329	missense	RNF213	GRCh38.p7	17:80343272	CTGCTGCCCTTCCTG[G/T]ATGCGCAGTATCAGA	57674
rs754436833	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80270162	CCCTGCGCATGCCTT[G/T]CTACTTTCATGTACA	57674
rs754448949	snp	A/G	3.29777e-05	0.00406051	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386402	GAAATTGTCTACGCC[A/G]TGGAAAAACTCTCCA	57674
rs754457764	snp	G/T	3.29495e-05	0.00405877	missense	RNF213	GRCh38.p7	17:80345629	ACCAGGCTTATTAAA[G/T]TCCTTAGCGACCTGC	57674
rs754458545	snp	A/G	1.64746e-05	0.00287002	missense	RNF213	GRCh38.p7	17:80291762	TCATTTACAAGCACC[A/G]GCAGAAGAAGGGCGA	57674
rs754459601	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376285	ACATCTTAATGTTAA[C/G]TTTTTTTCCTGTCAG	57674
rs754466330	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80318749	AGCTATATTTTTGTA[-/T]TTTTTTGTAGAGACG	57674
rs754498093	snp	A/C/T	5.06089e-05	0.00503014	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373121	CTCTCCAAGCCCGGC[A/C/T]GCCCGCACCAGTGGG	57674
rs754528876	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365797	TCATCATGTCTCGGC[A/G]CTCTGGGAGATGCAC	57674
rs754535335	snp	A/C	1.6625e-05	0.00288309	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383001	AAATTTTGACACAGA[A/C]TTGTCAACTAAAGAA	57674
rs754541993	in-del	-/TGT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381137	AGTTATACATCTTCA[-/TGT]TTCCCCCTGTGGCGT	57674
rs754551738	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80298232	TTGCTCTGTGTGCAC[A/G]GTGCTTGCTTCCTGT	57674
rs754565761	snp	C/G	0.00011411	0.0075526	missense	RNF213	GRCh38.p7	17:80334167	CCAGGAGCTCATCCA[C/G]GCCAAAAAGCTGCTC	57674
rs754567435	snp	C/T	3.33778e-05	0.00408507	synonymous-codon	RNF213	GRCh38.p7	17:80343253	GAGCCGAGTCCTGGG[C/T]GCCCTGCTGCCCTTC	57674
rs754572817	in-del	-/GAGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359557	AAAAAAAAAAAGAGT[-/GAGA]GAGGGAGGGAGACAG	57674
rs754574537	snp	A/G	0.000116689	0.00763747	missense	RNF213	GRCh38.p7	17:80346541	CTTTTTCTGGACGGC[A/G]TACCTCTGAGGAAAA	57674
rs754587227	snp	A/G	3.8219e-05	0.00437127	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351845	TTTATTTATGTATTT[A/G]TTTATTTATTTGTAT	57674
rs754593604	snp	C/T	1.65575e-05	0.00287724	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353055	GCCCGGAGACTTGCC[C/T]GAGCGTGAGTCACGA	57674
rs754600701	snp	A/C	1.6507e-05	0.00287284	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393353	TTTTCAGCCTGAGAG[A/C]CACTCTCGTAAGTTA	57674
rs754642980	in-del	-/GTTCCTC	2.44349e-05	0.00349526	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372512	TCTTTCTTGTTCCTT[-/GTTCCTC]AGGATTCAATACTTG	57674
rs754663699	snp	C/T	8.23947e-05	0.00641799	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288759	ACACACTGCCAGGTG[C/T]GTCTCCTTCCTGCCT	57674
rs754663746	snp	G/T	1.66482e-05	0.0028851	missense	RNF213	GRCh38.p7	17:80273318	GAGCTGAAGGAGGAA[G/T]GGGGCCCGTGCTTGT	57674
rs754678197	snp	C/T	1.64787e-05	0.00287038	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288584	CCATTGAGTCGGAGT[C/T]ACCCTGGCCCATTTT	57674
rs754679547	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280919	ACCTGGGGATGCGCA[C/T]GGAGCATGAGATGTG	57674
rs754690757	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386542	AGACACTCACTCCTT[C/T]AGCCGCCCCCACCAG	57674
rs754697267	snp	A/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377793	TCCTTGCTCCGTGGG[A/T]GAGGTGAGTCTTGGT	57674
rs754705618	snp	A/G	9.9557e-05	0.00705468	missense	RNF213	GRCh38.p7	17:80295611	GTACCATTGCCGGAC[A/G]GAAAAAGCACGGACT	57674
rs754706031	snp	A/C	1.71669e-05	0.00292971	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389110	GGCTCGGCTCTCTTA[A/C]CAGGTGGTGAGATGC	57674
rs754706033	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385913	TCAGGCAATCCACCC[A/G]CCTCGGCCTCCCAAA	57674
rs754723042	snp	C/T	1.6476e-05	0.00287014	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369613	TGAGAAGGAAGTGAT[C/T]GAGAGCCTGCTCTCT	57674
rs754728905	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360615	CGTTCTCAGAAGGCA[C/T]GAGCGCCTGGAGCAT	57674
rs754731678	in-del	-/TGG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359500	GCACTCTAGCCTGGG[-/TGG]TGACAGAGTGAGACT	57674
rs754733669	in-del	-/A	1.65018e-05	0.00287239	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375877	ACGCCAGAGGTGAGT[-/A]ACCGCCTGCAGGGCT	57674
rs754741396	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324065	AGTTTCACTTCTTCC[A/G]ATCTGGATGCCTTTT	57674
rs754747910	snp	A/G	6.59337e-05	0.0057413	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361751	CTGCCCAAGAAGTTC[A/G]TGGACATCTTTCAGC	57674
rs754749848	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80331166	TCTTCCTTATTTCAT[C/T]ACCACCTCCCAGTCT	57674
rs754752102	snp	C/G	1.74503e-05	0.00295379	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372566	TCCAGAAATGATGAA[C/G]TGAACCACCTAGAAG	57674
rs754769125	snp	A/G	1.64822e-05	0.00287068	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375756	GATACCCTTGATTTT[A/G]CAGGCCTGCAAGACC	57674
rs754773084	snp	C/G	1.64765e-05	0.00287019	missense	RNF213	GRCh38.p7	17:80344814	ATCTGTGGGAGTTCT[C/G]CAGCGAAACTTTCCA	57674
rs754780942	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	RNF213	GRCh38.p7	17:80346231	GAAAACAGAAGATGA[A/G]TGCAGCTTTGTCAGC	57674
rs754786999	snp	A/G	0.000154008	0.00877384	missense	RNF213	GRCh38.p7	17:80340074	GATCAGCTGAGCTAC[A/G]AGGTGGCACGCCAAG	57674
rs754794439	snp	A/G	1.64798e-05	0.00287047	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385191	GGCTCTGCTCTGACA[A/G]GACCAGGACTGTCCC	57674
rs754814740	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370519	CTGCTGGCCCCTCAC[A/G]TGAAGACACAGTAGC	57674
rs754829392	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80322827	TTTTCTCCCATTCTA[C/T]GTGTTGTTTTTTCAC	57674
rs754832963	snp	C/T	4.94376e-05	0.00497156	synonymous-codon	RNF213	GRCh38.p7	17:80346297	GTGGTTCCACGAGCA[C/T]AGCGCGATGCTCTTA	57674
rs754833690	snp	A/T	1.64996e-05	0.0028722	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388649	GACACGACTGGAACT[A/T]TGAACATCTCTTTAT	57674
rs754836453	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394555	ACTTAGGACCTCTCT[A/G]GACTAATTTCTCTTC	57674
rs754856012	snp	C/T	6.75083e-05	0.00580944	intron-variant	RNF213	GRCh38.p7	17:80273420	GTGAGTGCACTGCCT[C/T]GGCTCCCCTCCGCCC	57674
rs754883579	snp	C/G	4.94197e-05	0.00497066	missense	RNF213	GRCh38.p7	17:80290636	TCTTCATTTCCCATT[C/G]AATCCTGACCTCCAT	57674
rs754887686	snp	G/T	1.75256e-05	0.00296015	intron-variant	RNF213	GRCh38.p7	17:80350408	CTAAGTATGTTTTTA[G/T]TATTTTTCTCAGAAA	57674
rs754908313	snp	C/G	1.6476e-05	0.00287014	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361828	GCAGGAACTTCTTCA[C/G]TGTTACTTGAAGGAT	57674
rs754910625	snp	A/G	1.66535e-05	0.00288556	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372650	GCCAACGAGGCCTCG[A/G]TTGAATACCTGCAAG	57674
rs754912687	snp	G/T	1.65515e-05	0.00287671	missense	RNF213	GRCh38.p7	17:80340198	TCCCCTCTGCCTTCA[G/T]CCAGCACAAGGTCTT	57674
rs754924582	snp	A/G			missense	RNF213	GRCh38.p7	17:80332504	ATTGGATCAAGGACC[A/G]AGTCGAACAGATCAA	57674
rs754926840	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80290841	CTGAGACGGAGTCTT[A/G]CTGTGTCACCCAGGC	57674
rs754943648	snp	C/T	1.70752e-05	0.00292187	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354193	CCCACCCCTCTTGCC[C/T]CTGCCCCCACGTGGG	57674
rs754950720	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80333133	GGCTCACTGCAAGCT[G/T]CGCCTCCCAGGTTCA	57674
rs754968520	snp	C/G			missense	RNF213	GRCh38.p7	17:80309061	TACCTGACTGTGTGT[C/G]TGAAACTGCATGAAG	57674
rs754968841	snp	A/G	1.80322e-05	0.00300262	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288114	AGGAGTGGCCACAGG[A/G]AGTGAGGCTCAGAGC	57674
rs754970367	snp	C/T	1.65302e-05	0.00287486	missense	RNF213	GRCh38.p7	17:80295687	TGATTGTCCTTTTTG[C/T]AGTGGAAAAAATTGA	57674
rs754970771	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80263404	AACCCATGTTCTCAG[C/G]AGCAGGGATGGTTCT	57674
rs754997775	snp	A/G			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381687	GGTCCACCTCGTCCT[A/G]CGCAGGCTTCTCCAA	57674
rs755017019	snp	A/G	4.94262e-05	0.00497098	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368042	CCACGTGCACTGCCT[A/G]CGCTGCCTCAGGGCC	57674
rs755030173	snp	A/G	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80345323	AACATCAACGGCAGT[A/G]TCGATGCCATCAGTC	57674
rs755030616	snp	A/T	3.40084e-05	0.00412347	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385506	CAGGGGGTTGCTATC[A/T]TACGGTTCTTACCAA	57674
rs755041134	snp	A/G	1.67576e-05	0.00289457	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376565	GTAGGCCACAATTCC[A/G]TCGGCCTTCACTGGA	57674
rs755043029	snp	C/G	1.7056e-05	0.00292022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363582	GAGGGGCACCGCTCA[C/G]CCACGCCCTGCTGTC	57674
rs755067662	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80289237	GCACTGGAAGGTCCC[C/G]AGCGGGGAAGGGTCG	57674
rs755085829	snp	C/T	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390004	CATTTGCTCTTCCGT[C/T]GTTTTAGGAGCCATT	57674
rs755091431	snp	A/G	0.000117101	0.00765093	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354031	CAGGTGTCGATCCTG[A/G]ACACCACCAGGCTGC	57674
rs755118607	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381590	TGAGGGATCCAAAAG[A/G]CTTTCTGCAGCAGCA	57674
rs755126939	snp	A/G	3.29859e-05	0.00406102	missense	RNF213	GRCh38.p7	17:80313115	GAGAAGTTTTTACAA[A/G]GAACATGCTCACATC	57674
rs755127697	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364705	ATTTCATCACTAGGC[A/C]ATTACATTTTCCATG	57674
rs755138883	in-del	-/A	1.7739e-05	0.00297812	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351678	CTTTTTTTTTTCTTT[-/A]AAATAGGTATTCTGT	57674
rs755157543	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286070	TTTAGAGTCAGCCTG[C/T]GCTGGGAGTGAGTCT	57674
rs755160108	snp	C/T	3.30825e-05	0.00406696	missense	RNF213	GRCh38.p7	17:80346808	AGCACCTTCCGGCAG[C/T]GCGCCCGCTTTCAGC	57674
rs755174909	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80325918	CTACTCTCTTGAAAA[G/T]ATCATTTTTGTGTTA	57674
rs755175746	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389506	AACAACTGCTCACCC[A/G]GTCAGTCCAGCATAA	57674
rs755180968	snp	A/G	9.91654e-05	0.0070408	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369771	TTCTGGTTTAAGGAC[A/G]CTGTGAACACACAAA	57674
rs755187380	in-del	-/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354302	GACACAGTGGGAATC[-/T]TAAGAGCATCTCTCA	57674
rs755187396	in-del	-/AC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371769	TGTATATGTTTATAC[-/AC]ACACACACACACAGG	57674
rs755192641	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RNF213	GRCh38.p7	17:80294838	GAAGCAGATTGCCGC[C/T]GCGCTCATGCTGGAC	57674
rs755223323	snp	C/G	1.66427e-05	0.00288462	intron-variant	RNF213	GRCh38.p7	17:80263786	CATAGCAGGTGAGGC[C/G]CAGGGGTGCTGGTGG	57674
rs755231162	snp	C/G	1.64775e-05	0.00287027	missense	RNF213	GRCh38.p7	17:80306415	CATATCCTGGACTGT[C/G]TTTCAGGGATTTACT	57674
rs755237757	snp	C/G	1.69812e-05	0.00291382	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288187	GCTTCCATCCCCTCT[C/G]GGGGCAGAGGCCTGT	57674
rs755241729	snp	A/G	3.30038e-05	0.00406212	missense	RNF213	GRCh38.p7	17:80347870	CTGGATATCAACACG[A/G]TGCTGGAGAAATGGC	57674
rs755246125	snp	C/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80343881	GGAATTTGGGTGTTT[C/G]TTTTCAAGCTCCTCA	57674
rs755257940	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80281587	CACACCACTCACACA[-/C]CTGCCAACACACACA	57674
rs755262916	snp	A/G	3.29468e-05	0.00405861	missense	RNF213	GRCh38.p7	17:80294917	TTCTTCACCCAGTTC[A/G]AGCAGTTTTGCTTTG	57674
rs755270366	snp	C/T	3.2956e-05	0.00405918	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374422	TTGCAAGACATTCCT[C/T]CCATTGTTCACCCCC	57674
rs755273892	snp	A/G	1.64947e-05	0.00287177	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358463	CTGAACATTCCTCTT[A/G]TGATGAATAATGAAA	57674
rs755275808	snp	C/T	1.67167e-05	0.00289103	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363626	CCTGGACGCATTTGC[C/T]GCAATGGCCTGCACG	57674
rs755282548	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326517	TTGTCCATTCTCTGA[A/G]GTTTGGATAAACCAT	57674
rs755295192	snp	C/T	3.32945e-05	0.00407997	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369902	TTGCTTCTGGAAAGC[C/T]CTGGCTTTTTCTCTT	57674
rs755298235	in-del	-/AG	1.6477e-05	0.00287024	frameshift-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354495	TTTAAAGAAGCAAGA[-/AG]AGAGAGCCAGTTTCA	57674
rs755301373	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80269246	TCCTCTGACAACACC[C/G]TCACAGACACAACCA	57674
rs755306581	snp	A/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80306317	ACGAGCCTCTCTTCC[A/G]GTCCTGGTTTAGTCT	57674
rs755318187	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383810	CCCGGAAAAGTGTGG[C/T]CCATTGCTCTAAGAT	57674
rs755326317	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80294730	CTTAGACTGGCATCA[A/G]TACTATGACATAGTT	57674
rs755333156	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364343	TGGACCCCGGGTCCC[A/G]CATCTCTTCTCCCGT	57674
rs755333650	snp	G/T	0.000165637	0.00909896	intron-variant	RNF213	GRCh38.p7	17:80289634	AGGCCGGCCTTCAAG[G/T]TCAGGGTTTGGTTCC	57674
rs755333905	snp	C/T	1.64803e-05	0.00287052	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383904	CAAAGAAAGAGTGCC[C/T]ATCCTCTGGCATTTC	57674
rs755356974	snp	A/C	1.64936e-05	0.00287168	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353602	CAGAGGTGGCAGAGG[A/C]GGCCATGGAAACAGA	57674
rs755364950	snp	A/G	0.000114045	0.00755045	missense	RNF213	GRCh38.p7	17:80337943	TTTGAACAAGTTGAT[A/G]CTGATGTCTGGCAAG	57674
rs755389458	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268492	GGCCTTTGTGGAAGA[C/T]GGGTGGATCTTGGGA	57674
rs755395330	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373486	GTGATCATGTTTACA[C/T]TGCCTGCTGTAGGGC	57674
rs755405100	snp	C/G/T	3.29496e-05	0.00405881	intron-variant	RNF213	GRCh38.p7	17:80309010	TCTCTTAACTCTTTG[C/G/T]GGGGCAGGATTCCCG	57674
rs755408146	in-del	-/AC	1.66735e-05	0.00288729	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382994	GGCTTTTAAATTTTG[-/AC]ACAGAATTGTCAACT	57674
rs755441014	snp	G/T	3.30513e-05	0.00406504	missense	RNF213	GRCh38.p7	17:80289718	AAAAGTCGGTAAGAA[G/T]GAACAAGGGGAGCCT	57674
rs755445323	snp	G/T	1.64757e-05	0.00287012	intron-variant	RNF213	GRCh38.p7	17:80349756	CAAGTAATTTGCATT[G/T]CTTAACTCTGTAGAT	57674
rs755449744	snp	C/T	1.64866e-05	0.00287106	synonymous-codon	RNF213	GRCh38.p7	17:80345859	TGATCATATGGTGGA[C/T]GGCCAGCCTCTGGCT	57674
rs755452362	snp	C/T	9.88419e-05	0.00702931	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389253	TGAAGTGCTGTCTGT[C/T]GTAGAAGTCACTCTG	57674
rs755460716	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321032	ATTGTAGCTTGTGTC[C/T]GTTTACGTTAAGTAT	57674
rs755488244	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358866	GTGAGCCGAGATGGC[G/T]CCACTGCACTCCAGC	57674
rs755499802	snp	C/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80309076	CTGAAACTGCATGAA[C/G]CCATCTGCAGCAGCA	57674
rs755504553	snp	A/G	1.92424e-05	0.00310175	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363081	TTAAAAATATATTCT[A/G]AAAGCTTTTTTGAAT	57674
rs755510612	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397012	AAGGGTCCTACCTTC[C/G]CCAGTATTCCTTCAT	57674
rs755515057	snp	A/G	4.94874e-05	0.00497406	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369719	TCATTTCTTCATCTC[A/G]CTTCTGCATGTCTCA	57674
rs755516180	snp	A/G	3.38021e-05	0.00411095	intron-variant	RNF213	GRCh38.p7	17:80295859	ATAGCTATTATAATG[A/G]TTTTCTCTGATTGCA	57674
rs755527671	snp	A/C	4.94947e-05	0.00497443	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364538	GGTGACCGAGCACGT[A/C]TTCTTACTAGACAAG	57674
rs755529387	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392659	CAGTGGTGCAATCTC[A/G]GCTCACTGCAAGCTC	57674
rs755545642	snp	C/T	1.64866e-05	0.00287106	synonymous-codon	RNF213	GRCh38.p7	17:80345802	GTTTTTTGATGAAGC[C/T]AACACAACGGAAGCT	57674
rs755548404	snp	G/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320356	GTTGGTGGTGGTGGT[G/T]GTTTGTTGTTTTTGA	57674
rs755563616	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380866	AGACCGGCCACGTGC[C/T]GGGCAACCCGCAGCG	57674
rs755566083	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259182	CGTTCTAAAGTGTCA[C/T]CTTGGCTGGGCGCAG	57674
rs755567489	in-del	-/T	1.64939e-05	0.0028717	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386764	GGGACCTGACTCCAC[-/T]GATTCTCTCCAACTG	57674
rs755575749	snp	A/G	3.31159e-05	0.00406901	intron-variant, stop-lost	RNF213	GRCh38.p7	17:80319479	ATGGCGCTGAAATCT[A/G]GTTCTCTCCGGATTC	57674
rs755576540	snp	A/G	4.9476e-05	0.00497348	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388674	CTTTATGGACATCAA[A/G]AACAAAATGGCACAG	57674
rs755597730	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80277785	TGTATGCGTGAACGG[C/T]GCTCTAAGCGCAGAC	57674
rs755603047	snp	C/T	1.65231e-05	0.00287424	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383690	AGCATCTAGATAAAA[C/T]CCTTCCCACCATGAA	57674
rs755608314	snp	A/C/T	6.59189e-05	0.00574071	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288772	TGCGTCTCCTTCCTG[A/C/T]CTGCCGGCTCCAGGA	57674
rs755612784	snp	C/G/T	9.88524e-05	0.00702975	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376250	TATGTCTAAGAGCAA[C/G/T]TCACACAATATTCTT	57674
rs755614577	snp	A/G	1.65034e-05	0.00287253	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364403	TGGTGGGAGCCGAGT[A/G]AGTGAGTGAGTGGCG	57674
rs755617603	snp	A/G	3.29598e-05	0.00405941	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393469	TGGAAAACAGCTGCT[A/G]TGCTGAAATGGAATC	57674
rs755617844	snp	G/T	1.64762e-05	0.00287016	synonymous-codon	RNF213	GRCh38.p7	17:80344824	GTTCTGCAGCGAAAC[G/T]TTCCAAAGACCTTAC	57674
rs755636315	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80330349	AAGAGAAAGCCCTCA[A/C]AAGTGGGTTGGCCCT	57674
rs755642050	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287535	AAATCCATCTCAGTG[A/G]ATGTCCAATAAGCAG	57674
rs755665422	snp	G/T	1.64762e-05	0.00287016	missense	RNF213	GRCh38.p7	17:80345719	GCAGACATGATCTAC[G/T]CCAGAGTCAGGGAGG	57674
rs755712045	snp	A/G	4.94222e-05	0.00497078	missense	RNF213	GRCh38.p7	17:80344910	AAGGCTCTGTCGAAG[A/G]CACCCCGGAGGAATG	57674
rs755712261	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80261890	GGTGTGGTGGCGCAT[C/G]CCTGTAACTCCACCT	57674
rs755717469	snp	C/T	1.64746e-05	0.00287002	missense	RNF213	GRCh38.p7	17:80319271	AGTGTGGCCAAGACC[C/T]TCGAGAAATGCATCA	57674
rs755719620	in-del	-/GTTAA	0.000235658	0.0108524	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376279	TTGATACATCTTAAT[-/GTTAA]GTTAAGTTTTTTTCC	57674
rs755721937	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329363	ATTTTCCTTCTGAAG[C/T]TTCAATGTGCTGCGC	57674
rs755723739	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300576	TTGTTTTGTTTGAGA[C/T]GGAGTTTCGCTTTAT	57674
rs755734739	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367051	TGCAAAAAACCTAAA[C/T]GCCCATTAACCAGCA	57674
rs755735028	snp	A/G	1.68173e-05	0.00289972	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389119	CTCTTACCAGGTGGT[A/G]AGATGCCAGAAACCC	57674
rs755737354	snp	G/T	1.70971e-05	0.00292374	intron-variant	RNF213	GRCh38.p7	17:80289617	AAAAAAAGAAAATGT[G/T]GAGGCCGGCCTTCAA	57674
rs755747241	snp	G/T	1.64789e-05	0.0028704	intron-variant	RNF213	GRCh38.p7	17:80349732	TTGCAACCTTTCCTT[G/T]AAGTCTGGCAAGTAA	57674
rs755749394	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80314748	ATGGTGGTGATGGTG[A/G]TGGTGGAGGTACTGG	57674
rs755753067	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80342037	CTCCTGACCTTGAGT[G/T]ATCACCCGCCTCAGC	57674
rs755793068	snp	C/T	0.00011533	0.00759287	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361860	TCATTCTCTTGACCA[C/T]GCGTGTGTCAACGGA	57674
rs755798280	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80272140	AACACAAAAATTAGC[C/T]GGGTGTGGTGGCATG	57674
rs755799165	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375518	CAGCCTGGCAAACAT[A/G]GTGAAACCCCGTGTC	57674
rs755811697	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80299807	CTTACAAGTGAGAAC[C/G]TGCGGTATTTGGTTC	57674
rs755816017	in-del	ACTGCACTCCAGCCTGGGCGACACAGTGAGACTTCATCTC/CTGGGGGCCAAAAGGAAACTTCCTCCAAA			intron-variant	RNF213	GRCh38.p7	17:80297410	AGCCGAGATTGTGCC[lengthTooLong]AAAAAAAAAAAAAAG	57674
rs755821277	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270956	GTCTTTCCAGGATGC[A/G]CTGAGTGGCAGAAAC	57674
rs755830451	snp	A/C	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375837	GGCTATTTTGTACAG[A/C]TCCCACAATGCAAGC	57674
rs755830780	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352613	GCCAGTGTCCCCCAC[A/C]CCTCACTAACTGTGA	57674
rs755844429	snp	A/C	1.77489e-05	0.00297895	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385655	GTACCACTAAGCGTT[A/C]CAGGAGAGCCTCGTC	57674
rs755850556	snp	A/G	1.64798e-05	0.00287047	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361764	TCGTGGACATCTTTC[A/G]GCAGACTCCTCTGGG	57674
rs755851533	snp	C/T	0.000148257	0.00860851	synonymous-codon	RNF213	GRCh38.p7	17:80290645	CCCATTCAATCCTGA[C/T]CTCCATAAAGTCTTC	57674
rs755856902	snp	C/T	6.59402e-05	0.00574158	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364460	TCGGATTTTCTCCAC[C/T]GCACTCTTCGTGGAG	57674
rs755860737	snp	A/G	5.00872e-05	0.00500411	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379764	AAACTTTGGGGTGTT[A/G]GGCTGTTTTTATTCC	57674
rs755883280	in-del	-/T	1.64887e-05	0.00287125	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380844	GAGACAAGGCAGACA[-/T]GAACGCAGACCGGCC	57674
rs755899266	snp	A/G	3.31983e-05	0.00407407	intron-variant	RNF213	GRCh38.p7	17:80295829	GTATTATTATTTTTT[A/G]TCAAAATGTTTTTTA	57674
rs755900666	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80316072	ATAGATATTTGAACA[-/T]GCCTGACCTAAGAAA	57674
rs755906590	snp	C/T	1.65594e-05	0.0028774	synonymous-codon	RNF213	GRCh38.p7	17:80340223	GGTCTTCGTCACCCC[C/T]CAGGCACCCCTCGAG	57674
rs755912665	snp	A/G	1.66682e-05	0.00288684	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372666	TTGAATACCTGCAAG[A/G]GGTGGCCCGGATCCG	57674
rs755923601	snp	A/G	0.000193162	0.00982567	missense	RNF213	GRCh38.p7	17:80332068	AAAAGATTAAATGAC[A/G]CCGTGACAGTGAGAC	57674
rs755929593	in-del	-/GGGCAGT	1.68063e-05	0.00289877	intron-variant	RNF213	GRCh38.p7	17:80263808	TGCTGGTGGAGGCTG[-/GGGCAGT]GGGGACCCCTGGAGA	57674
rs755946158	snp	A/C	1.64732e-05	0.0028699	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390041	AATCAGTTCAAGGTA[A/C]AAAGCGGATCTGAGC	57674
rs755951298	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283118	TATAAATACCGCTAT[A/G]GTTATGTAGTTCGAG	57674
rs755954725	snp	C/T	6.59239e-05	0.00574087	synonymous-codon, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351799	CTATGTGGGCTTCCA[C/T]GGAGGTGAGATCAGA	57674
rs755970549	snp	A/G	1.69055e-05	0.00290731	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385510	GGGTTGCTATCATAC[A/G]GTTCTTACCAAGTAT	57674
rs755973119	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394081	ACAAGATCTGACCCT[C/T]TCCCCTCACAGTGAG	57674
rs755996239	snp	A/G	1.65067e-05	0.00287282	synonymous-codon	RNF213	GRCh38.p7	17:80347890	GGAGAAATGGCAGAA[A/G]AGCATCGTGGAGGAG	57674
rs755998023	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80312383	GGTCCGGCACGGAGG[C/T]GGGGGGAGAGCATGA	57674
rs756005463	snp	A/G	1.66966e-05	0.00288929	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363630	GACGCATTTGCCGCA[A/G]TGGCCTGCACGGAGA	57674
rs756045275	snp	A/C	1.65201e-05	0.00287398	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368158	GGTACAACACCCTTT[A/C]TCTCAAGAAAGCATC	57674
rs756046127	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371533	ATTTTAAATGAATGT[A/G]TATTTTTGAAACCTT	57674
rs756051971	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324338	TCAAATGCTTTTCCC[A/G]TATCTACTGAAATGA	57674
rs756077383	in-del	-/AAGG	1.65686e-05	0.0028782	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354589	CAGGTACTGTGACTA[-/AAGG]AAGCAAGGAGTGGCT	57674
rs756079875	snp	A/T	3.33317e-05	0.00408224	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351695	AATAGGTATTCTGTT[A/T]TAAATGAAATCAACA	57674
rs756130546	in-del	-/TATT	1.73246e-05	0.00294312	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80351839	GGGTATTTATTTATG[-/TATT]TATTTATTTATTTAT	57674
rs756136469	snp	C/T			missense	RNF213	GRCh38.p7	17:80334159	CAGATCAACCAGGAG[C/T]TCATCCAGGCCAAAA	57674
rs756165303	snp	A/G	4.94491e-05	0.00497213	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374509	TACCTGGTGTACGGC[A/G]ATGAATACAAGGCTC	57674
rs756174458	snp	G/T	5.19764e-05	0.0050976	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386848	AGATTCAGCGGCAGA[G/T]CGTCAGCCGCTTCCT	57674
rs756176629	snp	C/T	1.67995e-05	0.00289819	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376571	CACAATTCCATCGGC[C/T]TTCACTGGAACACCC	57674
rs756177790	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80303850	GCTGGGATTACAGGC[A/G]TGAGCCACCCACTGT	57674
rs756185803	snp	A/G	1.67424e-05	0.00289326	intron-variant	RNF213	GRCh38.p7	17:80263800	CCCAGGGGTGCTGGT[A/G]GAGGCTGGGGCAGTG	57674
rs756189338	snp	C/T	1.69836e-05	0.00291402	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381696	CGTCCTGCGCAGGCT[C/T]CTCCAAGAGCAGCAC	57674
rs756192421	snp	C/G	1.64789e-05	0.0028704	missense	RNF213	GRCh38.p7	17:80346067	CCGAGCCTGATTCCT[C/G]TGGTGTGGGACTTTG	57674
rs756204496	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386965	CTTGGTGTGTTTCTC[A/G]AGAGAGGGAAGCAGC	57674
rs756207567	snp	C/T	6.72823e-05	0.00579971	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360018	TTGTGTTTTGAGTGA[C/T]GTCTCACAAACCCTC	57674
rs756208639	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381954	CTGGAAGGAGCTGCT[C/T]TGTTCCCTCCATTCA	57674
rs756213942	snp	C/T	1.64808e-05	0.00287057	missense	RNF213	GRCh38.p7	17:80343993	GGAGGACGTCAGTGC[C/T]GTCGAGGAGCTCTTC	57674
rs756225987	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265760	TTCCAGGCATGCAGG[A/G]CGTCTGCTGTTAAAG	57674
rs756227605	snp	C/T	1.7067e-05	0.00292117	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288284	AGGAGCTCCTGTTGC[C/T]TGAGTCAAAAGGAGG	57674
rs756234171	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80272121	ACCCCTGTCTCTACT[-/A]AAAAACACAAAAATT	57674
rs756235883	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370556	TATTGTTTTCTTCAC[C/T]GCCATGCACACGTGG	57674
rs756244535	in-del	-/AC	5.02913e-05	0.00501429	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363689	TCCCCAGGCGTGGCT[-/AC]AGTTGGTGAAGAATC	57674
rs756264619	snp	G/T	1.67604e-05	0.00289481	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376938	AGCTCGGAGGTGGAA[G/T]GGTCTGGAGCGAGTC	57674
rs756265571	in-del	-/AG			intron-variant	RNF213	GRCh38.p7	17:80276611	GATCCTTCCTCAAAG[-/AG]AGAGAGAGAGAAGGA	57674
rs756269750	snp	A/C/T			intron-variant	RNF213	GRCh38.p7	17:80318862	ACAGGCGTGAGCCAC[A/C/T]GCGCCCGGCCTATAT	57674
rs756288806	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356368	ACTGAACCTCCTCAG[C/T]CTGCTCTTCCCCACT	57674
rs756289206	snp	A/C/G	3.29453e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80306351	ACCTCTGAGTCACCT[A/C/G]GTTATGTATATGGAA	57674
rs756292314	snp	C/T	3.29696e-05	0.00406001	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390107	TCAGACTGGCCTAGA[C/T]GCCTTCCTGCTAGAG	57674
rs756313201	snp	A/G	1.6504e-05	0.00287258	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364551	GTCTTCTTACTAGAC[A/G]AGGTGAGTACTTGGG	57674
rs756323371	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80302712	AACAAACAAAAAAAA[C/T]AGTTAGGCATGGTGG	57674
rs756331075	snp	C/G	3.75601e-05	0.00433343	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374616	CCGTGGCTTCTCTCT[C/G]ATACCAGGTGGCATC	57674
rs756332122	snp	C/T	8.24314e-05	0.00641942	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374517	GTACGGCGATGAATA[C/T]AAGGCTCTCCGTGAT	57674
rs756336687	snp	A/G	1.66258e-05	0.00288316	missense	RNF213	GRCh38.p7	17:80289737	CAAGGGGAGCCTGAA[A/G]ACCTCAAGAAGCCAG	57674
rs756375121	snp	A/G	0.000539578	0.0164164	intron-variant	RNF213	GRCh38.p7	17:80295041	CTCTACCTGCTGGGC[A/G]GGAGCCACACCTGAC	57674
rs756376690	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305701	ACTGCAATCTCTGCC[A/G]CCGGGGCTCAAGTGA	57674
rs756381121	snp	G/T	5.09083e-05	0.00504495	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353968	GGCGGTTTGGCTTTT[G/T]CCCACTGTGTCAGTG	57674
rs756408365	snp	A/G	0.000114006	0.00754916	synonymous-codon	RNF213	GRCh38.p7	17:80339362	GACGGAGCTTAAAGA[A/G]GGTGGAGATGTCACT	57674
rs756409502	in-del	-/T	1.6716e-05	0.00289097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388592	TTAATTTTAAAAAAC[-/T]TTTTTCTTTCCCAAT	57674
rs756413268	snp	C/T	0.000114097	0.00755217	synonymous-codon	RNF213	GRCh38.p7	17:80325125	GTCCTGGCCTAGGAC[C/T]GCGGACAACTTCAAT	57674
rs756415586	snp	A/G	1.64784e-05	0.00287035	intron-variant	RNF213	GRCh38.p7	17:80309191	GTGGAGTCAACACAC[A/G]AGGTATCACACCCGG	57674
rs756450994	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80286200	GCCTGGGGTTGGTGT[C/T]GGACGCAGGCCGGTG	57674
rs756451055	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389557	TAGAGACAGACACGC[A/G]CTAGAAATGCCAGCA	57674
rs756451900	snp	C/T	0.000131815	0.00811728	synonymous-codon	RNF213	GRCh38.p7	17:80346096	TGGACAACTGAGTGA[C/T]GTTGCTGAAAAGCTC	57674
rs756461345	snp	C/T	0.000114515	0.00756599	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287864	GGAACAAGTCCGCTT[C/T]CTCAGAGCTGGCTTC	57674
rs756461857	snp	C/T	4.94336e-05	0.00497135	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380875	ACGTGCTGGGCAACC[C/T]GCAGCGGAGAGACGT	57674
rs756465039	snp	A/G	4.94271e-05	0.00497102	synonymous-codon	RNF213	GRCh38.p7	17:80294943	CTTTGTCCTGCAACA[A/G]CCTATGATTTATGAA	57674
rs756471305	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328253	CGGGGAAGGTGCGGC[A/G]CTTTCAAAGCATTGC	57674
rs756493563	snp	A/G			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368054	CCTGCGCTGCCTCAG[A/G]GCCTGGTTTGCCTCA	57674
rs756493632	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80340897	GCAACCTTCGCCTCC[C/T]GGATTCAAGCGATTT	57674
rs756494048	in-del	-/AG			intron-variant	RNF213	GRCh38.p7	17:80271466	ATGAAGTGTCCAGAC[-/AG]GGGCGCAGCTGGGAC	57674
rs756497301	snp	A/G	1.64988e-05	0.00287213	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385022	AAATTGTTACTGGGT[A/G]GTCTTCCCTTCTCCA	57674
rs756499607	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328578	TTTATTTTGGAGAGA[A/G]GGCTTTAAAATTTTT	57674
rs756502609	snp	A/C	1.64727e-05	0.00286986	stop-gained	RNF213	GRCh38.p7	17:80349888	TTGACACCGAGTACT[A/C]ATTCCTCAAAGAAGT	57674
rs756505299	in-del	-/A	1.7704e-05	0.00297518	intron-variant	RNF213	GRCh38.p7	17:80298309	CACTGCGGGATCTTT[-/A]TTCCCTTCCAGCTGG	57674
rs756514849	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80345046	TCTCTTCTGCAATCC[A/G]AGTTTTATTGGCGAC	57674
rs756541218	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296709	TTGTTTTGAGACAGT[A/G]TCTTACTCTGTTCCC	57674
rs756562253	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318820	CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	57674
rs756565129	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80327639	GCAAGACCTAACCCT[C/T]GTGGGGGAAAGCAGA	57674
rs756565993	snp	A/C			missense	RNF213	GRCh38.p7	17:80295657	GCCCAGTGAGGAGTA[A/C]ACTGAAAACAGGCCT	57674
rs756574061	snp	C/T	1.64882e-05	0.00287121	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386344	ACGGGGCCTGGGCCT[C/T]TGTGCTACCGCTCTC	57674
rs756579755	snp	C/G	1.64819e-05	0.00287066	missense	RNF213	GRCh38.p7	17:80347647	GGTGTTGCTTCTCAA[C/G]CTGCAGAACCTCTAC	57674
rs756586534	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80269303	CATCCTTCAACCCAA[G/T]CAAATTGACACCTGA	57674
rs756590601	in-del	-/GGG			intron-variant	RNF213	GRCh38.p7	17:80275041	GGGTGTGTGTGTGTT[-/GGG]GGTGTGTGTTGGTGT	57674
rs756595777	in-del	-/G			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399140	GGAAAAAAAAAAAAG[-/G]GATGATTTAACTTTA	57674
rs756595787	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80334655	TTTTGAGACAGAGTC[-/T]TCGCTCTGTCGCCCA	57674
rs756602839	snp	C/T	1.64898e-05	0.00287135	stop-gained	RNF213	GRCh38.p7	17:80347528	TTCGAGGGGGACCAG[C/T]AGCCGGAGATTATTT	57674
rs756612314	snp	C/T	6.66245e-05	0.00577129	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354066	AAGCTGTGTGCAGAG[C/T]GCCGTGGGCATGCTC	57674
rs756616634	snp	C/G	1.66418e-05	0.00288455	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358255	CTCTGGTTCCTCTGA[C/G]CCGTGGTGGCCCATC	57674
rs756622231	snp	A/C	1.64925e-05	0.00287158	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389802	GAGACCTCAGCCCCC[A/C]CTCAGGAATTCTATT	57674
rs756638485	snp	A/G	1.64841e-05	0.00287085	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363162	GCGTCAGAAGCGCCC[A/G]AGGAAGAGGTTTCCT	57674
rs756666781	in-del	-/GGAT	1.64746e-05	0.00287002	splice-acceptor-variant	RNF213	GRCh38.p7	17:80309017	ACTCTTTGCGGGGCA[-/GGAT]TCCCGAGGAGGCCTT	57674
rs756714949	snp	C/G	1.64738e-05	0.00286995	synonymous-codon	RNF213	GRCh38.p7	17:80344983	CTGGTCAGAGCTTCG[C/G]AACTTTGCTCGGTTC	57674
rs756721685	in-del	-/CGG	2.471e-05	0.00351488	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381771	GATCACACAGCACAA[-/CGG]CAGCGCAAGCAGGCT	57674
rs756735067	snp	A/G	1.65343e-05	0.00287521	missense	RNF213	GRCh38.p7	17:80343146	GGAAAGTCTCTGTAC[A/G]TGAAGAGGTTGCACG	57674
rs756746622	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268738	ATCTATCCTATCTAT[C/T]CATCTATCTATAAGT	57674
rs756748119	snp	A/G	1.65162e-05	0.00287365	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385567	CTGCTTCACAACAGG[A/G]TCACAGTCTTTCTGT	57674
rs756759340	snp	C/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80309045	GGCCTTGTCACCATC[C/G]TACCTGACTGTGTGT	57674
rs756767720	snp	A/G	1.64781e-05	0.00287033	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361871	ACCATGCGTGTGTCA[A/G]CGGAGGAGGAATTAA	57674
rs756782842	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321214	TAGCCTGAAGGTAAT[C/T]TTATACAATATTTTT	57674
rs756785270	snp	A/C	1.66109e-05	0.00288187	stop-gained	RNF213	GRCh38.p7	17:80340253	GGCCATCCAAGCCTA[A/C]CTGGCAGGTCACTAC	57674
rs756790622	snp	A/G	1.64963e-05	0.00287192	synonymous-codon	RNF213	GRCh38.p7	17:80346396	CTGGTCGTTGATGCT[A/G]GCCATCGGGGTGTGT	57674
rs756802289	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394390	TCTAGTCCTTTCTGT[A/G]GTTCTCAGCCAAGAC	57674
rs756803192	snp	C/G	1.64876e-05	0.00287116	missense	RNF213	GRCh38.p7	17:80289707	GCTGCTGAAGAAAAA[C/G]TCGGTAAGAATGAAC	57674
rs756805187	snp	A/C	1.66189e-05	0.00288256	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389130	TGGTGAGATGCCAGA[A/C]ACCCAGCCCACAGAC	57674
rs756808414	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384631	GCAGTTTCACTACGT[A/C]GAAGATGCTTAGATC	57674
rs756811985	snp	C/T	1.64925e-05	0.00287158	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319405	GCACCCGCTGGGTCT[C/T]AGCTCCTCCGCTAAC	57674
rs756831813	snp	A/G	1.64765e-05	0.00287019	intron-variant	RNF213	GRCh38.p7	17:80349747	GAAGTCTGGCAAGTA[A/G]TTTGCATTTCTTAAC	57674
rs756832892	snp	C/G	1.65225e-05	0.00287419	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380782	GAAAGTGCAGCGTGC[C/G]AAAGCGGCCAGCCTC	57674
rs756835906	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369257	TACAAAATTAGCCAG[G/T]CGTGATGGTGCGTGC	57674
rs756838073	snp	C/T	1.84527e-05	0.00303744	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385667	GTTCCAGGAGAGCCT[C/T]GTCTGAAAGCTCTTC	57674
rs756840887	snp	A/G	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345959	CGTTTGGAGTCAGCT[A/G]GTTTGGGCTACAGGG	57674
rs756849129	in-del	-/G	1.66474e-05	0.00288503	frameshift-variant	RNF213	GRCh38.p7	17:80273318	GAGCTGAAGGAGGAA[-/G]GGGGCCCGTGCTTGT	57674
rs756884764	snp	A/G	2.2894e-05	0.00338327	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287845	AGGAAGAAGAAAAAG[A/G]AGGGGAACAAGTCCG	57674
rs756888763	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362935	CGGTGACCTTAACGT[A/G]GGAGGAGAGGCAGAT	57674
rs756893436	snp	A/C	1.64808e-05	0.00287057	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368084	AGAGCAGATGATATG[A/C]CCCTACTGTTTAACT	57674
rs756898787	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312083	CAGTGAGCCAAGATC[A/G]CGCCACTGTACTCCA	57674
rs756901227	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80335425	GCTCTGGCTCTCTTG[C/G]GAGAGCCGCTGCTTT	57674
rs756903020	snp	C/T	1.8248e-05	0.00302054	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372761	CTGCCTTGCTTTCCT[C/T]TGGGTTTAAAGACTC	57674
rs756906218	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80331765	GAGAGTAAATAGGTG[C/T]GTGTTTTCCCACTGC	57674
rs756917892	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80263025	GCCAAGCGCCCAAAC[A/G]CCATCTCCACTCTCA	57674
rs756919069	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330825	TGCTGGATGGACCAT[A/G]TCTTTTTTTTGGGAC	57674
rs756924578	snp	A/G	1.74876e-05	0.00295694	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372990	AGATGGCCAAGGAGA[A/G]GCAGTGCTACCTGCA	57674
rs756945622	snp	A/C	1.65496e-05	0.00287655	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354580	GGGCACATTCAGGTA[A/C]TGTGACTAAAGGAAG	57674
rs756957762	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290222	GGGTGGTGTGTCACA[C/T]GTGGACGTGCTTGCA	57674
rs756976237	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394368	TGTGCTCTCGCATGT[A/G]TGAATATCTAGTCCT	57674
rs756981914	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392844	ATCCACCTGCCTCAG[C/T]CTCCCAAAGTGCTAG	57674
rs756982963	snp	G/T	1.65192e-05	0.00287391	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369454	TCATTCTGTAAGGAG[G/T]CATTTGGGAAACACC	57674
rs756994119	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80343443	GCACAGTCCTGTGAA[A/G]CTTAACAGTGGGAAT	57674
rs757000647	snp	C/T	2.04929e-05	0.00320094	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363077	TAATTTAAAAATATA[C/T]TCTAAAAGCTTTTTT	57674
rs757005908	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272839	TGAGACCCCTGGGCC[A/G]CCACTGGGAGAATGC	57674
rs757008952	in-del	-/C	1.64735e-05	0.00286993	frameshift-variant	RNF213	GRCh38.p7	17:80291637	CACAGAGACTTGGGT[-/C]CATGACCGCGTTCTT	57674
rs757009101	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80342305	ATGCATTTTTCAGAA[C/T]GTGTCCCTAGTGCTA	57674
rs757011918	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380018	ATATGCATGACATAA[A/G]CAGATGATCTAATTC	57674
rs757023791	snp	A/G	6.64916e-05	0.00576553	intron-variant	RNF213	GRCh38.p7	17:80317139	TCATGGGAGTGTGCC[A/G]TGGCATTTAGTCGTG	57674
rs757028941	snp	C/T	8.37612e-05	0.00647098	intron-variant	RNF213	GRCh38.p7	17:80295848	AAATGTTTTTTATAG[C/T]TATTATAATGATTTT	57674
rs757045657	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300698	AGCTGGGACCACAGG[C/T]ACCCCACCATGCCTG	57674
rs757086130	snp	A/G	1.64808e-05	0.00287057	missense	RNF213	GRCh38.p7	17:80345554	AAAATCCTTGCCATC[A/G]AGATGCGGTTCCGGT	57674
rs757098705	snp	C/T	1.76836e-05	0.00297347	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381715	CAAGAGCAGCACCAG[C/T]TCTCTAGCAGAAGTG	57674
rs757110713	in-del	-/GGAAGAAGCGGGGTGAACGGTAATGGGGGCTTACAGG	0.00204822	0.0319361	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355307	CAGGAGGGAACGTGA[lengthTooLong]GGAAGAAGCGGGGTG	57674
rs757114739	snp	C/T	1.64852e-05	0.00287094	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390109	AGACTGGCCTAGACG[C/T]CTTCCTGCTAGAGCT	57674
rs757117809	snp	C/T	1.64874e-05	0.00287113	intron-variant	RNF213	GRCh38.p7	17:80307082	CAATGACAGTGGCAT[C/T]GTGATTCAATCTTTT	57674
rs757133661	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374144	GACTACCACCTGGGG[-/T]TTAGAGTTGACATGA	57674
rs757139775	snp	A/G	1.64874e-05	0.00287113	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351812	CACGGAGGTGAGATC[A/G]GAACATCAGTCAGGG	57674
rs757150044	snp	C/G	4.95086e-05	0.00497512	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352932	GTGGGTGGCTTCACT[C/G]TTCACAGGGCTGTGG	57674
rs757150171	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398223	TCTGATTTTGGTTTT[C/G]ATTTTGGTTTGGTGT	57674
rs757156944	snp	A/G	1.72285e-05	0.00293495	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363764	AGGCAGCGGGAGCCT[A/G]GCCCAGGCTGTCATC	57674
rs757174029	snp	A/G	3.29772e-05	0.00406048	missense	RNF213	GRCh38.p7	17:80345425	GTGCCCTTCAATGTC[A/G]ACTTTGATAAACTGC	57674
rs757185747	snp	C/T	0.000150069	0.00866094	intron-variant	RNF213	GRCh38.p7	17:80273228	CTGACCCTTCCTTCA[C/T]CTGCCGTTACAGATT	57674
rs757209392	snp	A/C/G	0.000144362	0.00849484	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377011	CTTTGAGCTTCAAAG[A/C/G]GTGTCCAGATGCTAT	57674
rs757215115	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284318	GCAATGGGCTCAGAT[C/T]ATGCCATTGCACTCC	57674
rs757229269	snp	A/C	0.00110921	0.0235239	stop-gained	RNF213	GRCh38.p7	17:80347998	CGTCTTCATCGGCTA[A/C]CACTCGGACGCCTGC	57674
rs757232815	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375554	AAGAAAAAAAAAAAG[-/G]AATTAGCCGGACATG	57674
rs757233464	snp	C/T	1.71179e-05	0.00292552	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288300	TGAGTCAAAAGGAGG[C/T]AGCTCTGAGCCCGGG	57674
rs757236540	in-del	-/GAGTGAGT	0.000231134	0.0107477	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364399	TCCTTGGTGGGAGCC[-/GAGTGAGT]GAGTGAGTGGCGCCC	57674
rs757244125	snp	A/G/T	5.05304e-05	0.00502624	intron-variant	RNF213	GRCh38.p7	17:80295510	CTGGACACTGCCGGT[A/G/T]AATTCAAGTCCATGG	57674
rs757249090	snp	A/G	6.71584e-05	0.00579437	intron-variant	RNF213	GRCh38.p7	17:80317311	CAGTCTTTTCAGGGC[A/G]TGAAGGCAAGCTGGA	57674
rs757291180	snp	C/T	0.000114397	0.0075621	missense	RNF213	GRCh38.p7	17:80339436	ACAGCTGGAAGAGAT[C/T]TGTGACCCAGAAGCG	57674
rs757305285	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294455	TGCAAGTCTCAGGCC[C/T]GCTGCATCCCATGAC	57674
rs757308535	snp	A/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352058	CGGGGTTTCACCACG[A/T]TGGCCTAGATGGTCT	57674
rs757308579	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362624	GCGTGCACAGTGGGC[A/G]CCCTGCAGGGCTGCG	57674
rs757309698	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396892	GACTGGAGGGGCCCT[A/G]GGTCCAGCAAGTGCT	57674
rs757318605	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80270460	GCTTCTCTGGCCACT[A/C]ACTGGCCGCGTCTCT	57674
rs757330419	snp	C/T	1.64893e-05	0.0028713	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374527	GAATACAAGGCTCTC[C/T]GTGATGCTGTGGCCA	57674
rs757337960	snp	C/T	1.64814e-05	0.00287061	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385036	TGGTCTTCCCTTCTC[C/T]AGGAAGCAGAGCTGA	57674
rs757339387	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267094	TGGTGGCTCATGCCT[A/G]TAATCCCAGCTTCTT	57674
rs757339392	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366188	GGGCAGGAAGTTGTC[A/G]ACGGAACTGCTGCAG	57674
rs757359936	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372125	AAAGGTTTCAAAGAC[A/G]CGGCTTCTGCCTTCA	57674
rs757362658	snp	C/T	3.30764e-05	0.00406659	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383963	GCTCCCTCCCTCTTT[C/T]GGTGCAGAGTTCCCC	57674
rs757387561	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389693	GATGGCCTTCACAAG[A/G]AGGGAGATCACATTA	57674
rs757391348	snp	A/G	1.65767e-05	0.00287891	missense	RNF213	GRCh38.p7	17:80347068	CGAGACAGAGCTCAT[A/G]GAGAGCGCCAAGGGC	57674
rs757392999	snp	C/G	2.71197e-05	0.00368227	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386902	TCAAGGTAGGGCTGA[C/G]TCCTGCCACTGCTGC	57674
rs757413615	snp	C/T	2.20524e-05	0.0033205	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360224	GAGGCTACCTCAAGA[C/T]AGGTCAGATTCAGCA	57674
rs757414482	snp	A/G	1.64806e-05	0.00287054	intron-variant	RNF213	GRCh38.p7	17:80344635	AAAAGCATTTCTTAG[A/G]AAGTCTTCTTGTAAC	57674
rs757427143	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80277546	GAGGTTGCAGTGAGC[C/T]GAGATTGAGACACCG	57674
rs757434448	snp	A/T			missense	RNF213	GRCh38.p7	17:80347207	CTTCGTGACTACTAC[A/T]GCCTCATCAAAATGG	57674
rs757442872	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80307595	ACTCTTGTTGCCCAA[A/G]CTGGAGTGCAATGGC	57674
rs757483398	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80290473	CATGTGTGTGTGCAC[-/GT]GTGTGTGCGCACGTG	57674
rs757498797	snp	A/C	1.65004e-05	0.00287227	missense	RNF213	GRCh38.p7	17:80313087	ACCCTTGCTGCTACG[A/C]AAAGGTGGCTCCGAG	57674
rs757502522	snp	A/C	5.61005e-05	0.00529595	intron-variant	RNF213	GRCh38.p7	17:80350260	CTTTTCCATTTTTTT[A/C]AGACAGAGAACTCAC	57674
rs757505353	snp	C/T	1.66322e-05	0.00288371	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354077	AGAGCGCCGTGGGCA[C/T]GCTCAGAGACCAGAA	57674
rs757507619	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265876	GGAGTTTGAGACCAG[C/T]CTGGGCAATGTAGAA	57674
rs757513532	snp	A/C	1.66007e-05	0.00288098	missense	RNF213	GRCh38.p7	17:80295590	CAACATCTGAAAAAA[A/C]ACGTGGTACCATTGC	57674
rs757522867	snp	A/T			missense	RNF213	GRCh38.p7	17:80345846	AAGAAGTCCTGTGTG[A/T]TCATATGGTGGATGG	57674
rs757529504	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305987	ATTTTTGTTTTCCAC[A/G]TAGCCTTTATTTTAT	57674
rs757541681	snp	A/G	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80290539	GGACAGATCTCACGG[A/G]AATCAGATTTCTGTT	57674
rs757541692	snp	A/G	5.35863e-05	0.00517593	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287994	CCCCACTGGCCAGCC[A/G]AGCCAGCCCCCAGGC	57674
rs757544522	snp	A/T	0.000192141	0.00979968	missense	RNF213	GRCh38.p7	17:80325130	GGCCTAGGACCGCGG[A/T]CAACTTCAATGACAT	57674
rs757552658	snp	A/C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260278	GCCGCAGACACTGTC[A/C/T]GAGGTGCTGGGCGCC	57674
rs757552706	snp	C/G/T	3.31007e-05	0.0040681	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367739	ACTCCTGTCCCTGCC[C/G/T]TTCTTCAGTGTCTTC	57674
rs757553323	snp	C/T	1.65674e-05	0.00287809	missense	RNF213	GRCh38.p7	17:80298499	TCCTTCTCACCGTTC[C/T]GGGAACAAATGCTAG	57674
rs757553708	in-del	-/C	3.29663e-05	0.00405981	intron-variant	RNF213	GRCh38.p7	17:80309202	ACACAAGGTATCACA[-/C]CCGGGATAGGTGCGG	57674
rs757567845	snp	C/T	1.6476e-05	0.00287014	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376471	CATTCATGCTGCAGC[C/T]GTCCTTCTGTGTGGA	57674
rs757605279	snp	C/G	2.0123e-05	0.00317192	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372525	TTGTTCCTCAGGATT[C/G]AATACTTGAGAAGAC	57674
rs757617499	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319557	TCCATATGGAATCAC[A/G]GCCGTGCGCGTGTGG	57674
rs757622575	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382024	GCACGCAAGTGTTCA[C/G]TGTGCATATATGGGG	57674
rs757630871	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389914	GCTGCTGCGGCTGCA[C/T]AAAGTAAGTCTGGTC	57674
rs757641527	snp	C/T	1.66007e-05	0.00288098	intron-variant	RNF213	GRCh38.p7	17:80312985	CACAGCCGAGGATGA[C/T]TGACCCTCCCTCTTG	57674
rs757643496	in-del	-/C	6.76642e-05	0.00581614	frameshift-variant	RNF213	GRCh38.p7	17:80346955	TTGAAGACGATCCCG[-/C]CCCCCCACAAAAAGG	57674
rs757663641	snp	C/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287347	CAAAAAACAAACCAA[C/G]AAAAAATTAGCTGGG	57674
rs757678722	snp	G/T	1.64803e-05	0.00287052	missense	RNF213	GRCh38.p7	17:80347730	AGTACGTGGACCTCG[G/T]TCTGGGGACCCACCG	57674
rs757686757	snp	A/G	1.64909e-05	0.00287144	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386405	ATTGTCTACGCCGTG[A/G]AAAAACTCTCCAAGG	57674
rs757712289	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365672	ATGTTCCAGGTGGAA[C/T]TTGAGTTCTTCTGCT	57674
rs757723915	in-del	-/AGCT			intron-variant	RNF213	GRCh38.p7	17:80334509	CCCCGCCACTTCGGA[-/AGCT]AGCTGTAAATGGCTC	57674
rs757733788	snp	C/T	1.66299e-05	0.00288352	missense	RNF213	GRCh38.p7	17:80350375	ATGGAATCCGTAGCG[C/T]CCAGCTCATTGCCTC	57674
rs757737720	snp	C/T	1.64827e-05	0.00287073	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389816	CACTCAGGAATTCTA[C/T]TCCTTCTGCAGGCCT	57674
rs757738943	snp	A/G	0.000150596	0.00867612	synonymous-codon	RNF213	GRCh38.p7	17:80340091	GGTGGCACGCCAAGC[A/G]GAGGAGCTTTTCCAC	57674
rs757739289	snp	C/T	6.59185e-05	0.00574064	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358440	TTATTTTCAGTGACA[C/T]GATGCTTCTGAACAT	57674
rs757751601	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298166	GGGGGCTGAGGGAAG[C/T]CCTGTCTCCTGCGTG	57674
rs757765642	snp	C/T	1.64768e-05	0.00287021	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369630	AGAGCCTGCTCTCTC[C/T]CCTCTTCGTCCAAAA	57674
rs757766505	snp	C/T	3.29592e-05	0.00405938	synonymous-codon	RNF213	GRCh38.p7	17:80347674	CTACGAGAGCCTCTA[C/T]GACGCACTCAACCAG	57674
rs757766811	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80339134	GTAGGCCTGTGTGCT[A/G]TTGCAGAGTAGCGTG	57674
rs757772582	snp	A/G	4.96693e-05	0.00498319	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386646	TAGAGCCCTAGGCCC[A/G]CATGCCTGGCCTGGA	57674
rs757791430	snp	C/G	1.64955e-05	0.00287184	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363151	AACTGAAAGCGGCGT[C/G]AGAAGCGCCCGAGGA	57674
rs757807981	snp	C/T	3.35531e-05	0.00409578	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373021	GCAAGTCAAGCAGTT[C/T]TGTATCCGGGTGGAG	57674
rs757812370	snp	C/T	1.71047e-05	0.00292439	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363575	CCGGTGGGAGGGGCA[C/T]CGCTCAGCCACGCCC	57674
rs757819404	snp	G/T	1.64942e-05	0.00287173	intron-variant	RNF213	GRCh38.p7	17:80306206	TCCATTTTCCCTCAC[G/T]GATCTCACTGCGTCT	57674
rs757820833	snp	C/T	1.68963e-05	0.00290652	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373125	CCAAGCCCGGCCGCC[C/T]GCACCAGTGGGTGTT	57674
rs757828908	snp	C/T	4.38433e-05	0.00468185	intron-variant	RNF213	GRCh38.p7	17:80343348	CCCTCCAGCGTCAGC[C/T]GATGGCCACATCAGT	57674
rs757833785	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295324	GGGTGGGTTTCAGGC[C/T]GGCCTGGAGCTGTTT	57674
rs757836545	snp	C/T	5.01735e-05	0.00500842	intron-variant	RNF213	GRCh38.p7	17:80343124	TAATTTCTGTATTAA[C/T]GTTATAGGAAAGTCT	57674
rs757859532	in-del	-/T	3.33356e-05	0.00408248	intron-variant	RNF213	GRCh38.p7	17:80295837	TTTTTTGTCAAAATG[-/T]TTTTTTATAGCTATT	57674
rs757867921	snp	A/C	3.31675e-05	0.00407218	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354596	TGTGACTAAAGGAAG[A/C]AAGGAGTGGCTCCAA	57674
rs757871150	in-del	-/TAAATCCTTGCCGGGATTTCTCTT	1.64788e-05	0.00287039	intron-variant	RNF213	GRCh38.p7	17:80308977	TTTTCTGGCTTCTCC[-/TAAATCCTTGCCGGGATTTCTCTT]AACTCTTTGCGGGGC	57674
rs757880599	snp	C/T	3.30142e-05	0.00406276	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386324	GAGATCCTCTTGCCA[C/T]GCCGACGGGGCCTGG	57674
rs757889244	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80297711	AGAATGGCGTGAACC[C/T]GAGAGGCAGAGCTTG	57674
rs757890987	snp	C/T	0.000228389	0.0106837	missense	RNF213	GRCh38.p7	17:80336335	AGCATCTGAAAAAGC[C/T]GTGGAAGGCTCTGGA	57674
rs757894386	snp	C/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80258881	AGGCAAAGCTCCAAG[C/G]GCTTAGTGTACCTGC	57674
rs757908465	snp	A/G	0.000116707	0.00763804	missense	RNF213	GRCh38.p7	17:80332363	TTAAGTTGCACCAGG[A/G]TCTAAAGTCAGGAGA	57674
rs757934959	snp	C/T	1.88645e-05	0.00307114	stop-gained	RNF213	GRCh38.p7	17:80340344	ATCGTGGCCTCGGAG[C/T]GAGCAGGTGTTGGTA	57674
rs757935102	snp	C/T			missense	RNF213	GRCh38.p7	17:80337846	AGATTTCCCCAGACA[C/T]GGTTCTGCACTTGAT	57674
rs757938118	snp	C/T	1.65181e-05	0.00287381	missense	RNF213	GRCh38.p7	17:80298406	CTGCCTGTCCTGCAC[C/T]GCTGTATGGAGCTGG	57674
rs757941385	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80274956	GTGTGTGAGTGGGGG[-/G]TGTGTGTGTTGGGGT	57674
rs757942353	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270237	GGCTCTGCCACCCAG[C/T]AGGGCCTGACTCAGC	57674
rs757944852	snp	G/T	1.6477e-05	0.00287024	synonymous-codon	RNF213	GRCh38.p7	17:80345562	TGCCATCGAGATGCG[G/T]TTCCGGTGTGGGATC	57674
rs757948563	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386451	TGCACGAGCCACCAG[C/G]AAGTGGTGCCTGCTC	57674
rs757955875	in-del	-/GC			intron-variant	RNF213	GRCh38.p7	17:80323840	CTTTTTTTTGGGGGG[-/GC]GGGTGCTATTGTAAT	57674
rs757970200	snp	A/C	1.64879e-05	0.00287118	synonymous-codon	RNF213	GRCh38.p7	17:80347509	GATCCTGCAGCAGAC[A/C]TTCTTCGAGGGGGAC	57674
rs757991356	snp	A/G	3.29462e-05	0.00405857	missense	RNF213	GRCh38.p7	17:80345140	ACACCATCACTCCAC[A/G]CCTCTGACCAAAGCC	57674
rs757996314	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394571	GACTAATTTCTCTTC[C/T]TAGACAGCTCAGCAC	57674
rs758003191	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360485	ATGGCCAGGGATATG[A/G]CGAAATGGGGTGTGT	57674
rs758008785	in-del	-/A			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370304	GGAAAGGATGTTGAC[-/A]TCCAAGAATAGTATC	57674
rs758018407	snp	A/G	1.66679e-05	0.00288681	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358245	CAGACCGCCACTCTG[A/G]TTCCTCTGACCCGTG	57674
rs758024366	snp	C/T	0.000114201	0.00755562	synonymous-codon	RNF213	GRCh38.p7	17:80334116	GCAGACTGATAACTT[C/T]GACGACTTTCGCCGT	57674
rs758036652	snp	A/C	1.65135e-05	0.00287341	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369467	AGGCATTTGGGAAAC[A/C]CCATCCACCTGTCTT	57674
rs758042974	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321435	CATCTATGTTGCTTC[C/T]TCGGCTATTATAAAT	57674
rs758061621	in-del	-/TGCTC			intron-variant	RNF213	GRCh38.p7	17:80291944	CAGTGAGGTCCTCTT[-/TGCTC]TGCATTGACCCCGCC	57674
rs758066114	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369541	CTTCCGGCAGATGTG[C/T]AACAGTTTCTTCGTA	57674
rs758076423	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394471	AGGGAAAAGAGTCCC[C/T]GAGCCCGGATCTTGT	57674
rs758079303	snp	C/G	3.29935e-05	0.00406149	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390120	GACGCCTTCCTGCTA[C/G]AGCTGCACGAAATGA	57674
rs758093056	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359799	GACTTGGTTCTGCCC[A/G]AGATTTTGGGCAACA	57674
rs758105652	snp	A/G	8.24967e-05	0.00642196	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352960	TGGCAGTCTGTCCAC[A/G]TCGATGACCTCCGGA	57674
rs758111715	snp	A/T	1.69838e-05	0.00291404	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382968	CCTACACATTTGGAG[A/T]TTTTTTGTAGGGCTT	57674
rs758114180	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80291724	GTACGTCATTTATAA[C/T]GGGGAATCTTTTGAG	57674
rs758120239	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280017	CATGTGTTCATTGAA[C/T]GGAGACTTACCGAGC	57674
rs758123491	snp	C/G	1.64749e-05	0.00287005	missense	RNF213	GRCh38.p7	17:80319207	GGAACCCCTCTCCCA[C/G]ATCACTGCCTACTGC	57674
rs758123547	in-del	-/C	1.68775e-05	0.0029049	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367710	GCCGCCCTCAGCCCT[-/C]CCCCCTGCTAATGAC	57674
rs758132340	snp	C/T	0.000197658	0.00993931	synonymous-codon	RNF213	GRCh38.p7	17:80291646	CTTGGGTCATGACCG[C/T]GTTCTTGTTGAAGGC	57674
rs758145646	snp	A/C	1.726e-05	0.00293763	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363767	CAGCGGGAGCCTGGC[A/C]CAGGCTGTCATCAGG	57674
rs758158253	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80264301	GAGAGCTCTGCCTGG[A/G]TTAGTTTTTGAGGGG	57674
rs758161641	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80301772	CTGTATGATCCAGCA[A/G]TCGTACTGCTGGGGA	57674
rs758169561	snp	A/G	3.32602e-05	0.00407786	intron-variant	RNF213	GRCh38.p7	17:80273234	CTTCCTTCATCTGCC[A/G]TTACAGATTCTGAGA	57674
rs758175471	snp	C/T	5.0048e-05	0.00500215	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373062	ACCGGGTGTACCTGG[C/T]GCGGAAGCTCAGCAG	57674
rs758179297	snp	A/G			missense	RNF213	GRCh38.p7	17:80332431	TTTGTGAATAAATAC[A/G]CGGACCTGGATTCAG	57674
rs758199422	snp	A/C/G	0.000155306	0.00881083	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383096	AGTGCTGACAGCTGG[A/C/G]TTGCTCCTCGGTCCA	57674
rs758202246	snp	G/T	1.64738e-05	0.00286995	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385081	CTGCCTGAGATTTTG[G/T]CCTTGCAAAGGGATC	57674
rs758211305	snp	C/T	1.64776e-05	0.00287028	intron-variant	RNF213	GRCh38.p7	17:80344653	GTCTTCTTGTAACCA[C/T]TTCATTAATGTCTCT	57674
rs758219329	snp	A/C	3.29451e-05	0.00405851	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377714	CTTTTCAATGTGGGT[A/C]ATTGGGTGAAACCTC	57674
rs758219806	in-del	-/AAT	3.30235e-05	0.00406333	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372484	ATCCATGTTTAAAAA[-/AAT]AATATCCTTTTCTTT	57674
rs758223575	snp	C/G	1.64746e-05	0.00287002	synonymous-codon	RNF213	GRCh38.p7	17:80345616	TGGCTGTGGGAAAAC[C/G]AGGCTTATTAAATTC	57674
rs758246618	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80263273	CCCTTAAGAGGATGA[C/G]GAGGGTGAGGCATCA	57674
rs758263535	snp	C/T	1.67083e-05	0.00289031	synonymous-codon	RNF213	GRCh38.p7	17:80273386	GCCCTGTTCCAAAGC[C/T]TCCTGGACCGTCCAA	57674
rs758269591	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331843	TTAACAAGGCCAAGC[A/G]GGGAGGGAAAGACCT	57674
rs758274742	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368234	TAAACTCTATTAACC[A/T]TCATTTGGTAGAAAA	57674
rs758304308	snp	C/T	4.99821e-05	0.00499885	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390183	ACCGAGGAGCGCTTC[C/T]GCCCTCAGTGGAGGT	57674
rs758312616	snp	C/T	6.62658e-05	0.00575574	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375728	GATGTGTTGAGCTTT[C/T]AAATTCTTACTTGAT	57674
rs758315053	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80330320	CTGGACATTCTTGTT[C/T]GTCTGTGTTTATTAA	57674
rs758320984	snp	G/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80344779	GAGTGCCCTGAGGAG[G/T]GACACAGAGCCTGGG	57674
rs758334923	snp	C/T	0.000215034	0.0103668	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353043	CCAGCTGTTCGCGCC[C/T]GGAGACTTGCCTGAG	57674
rs758335811	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80300921	TCATATGCCTGTTAG[C/G]CACATGTATGTCTTC	57674
rs758341034	snp	A/G	3.30213e-05	0.00406319	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388639	CTGGTGTACAGACAC[A/G]ACTGGAACTATGAAC	57674
rs758349838	snp	A/T	1.65679e-05	0.00287814	missense	RNF213	GRCh38.p7	17:80313013	TTGTGTGACAACAGG[A/T]TTCTGCAGGACAGAG	57674
rs758359060	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80343515	TGAACGTCATGGTGT[C/G]CGCTTACACTAACCT	57674
rs758360159	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80272925	CTCTGTTTTAGAGGT[G/T]CCCGAGGTGCGCTGA	57674
rs758363708	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272344	GTTTATTTAGCTCAC[A/G]GTTCTGCAGACTGAG	57674
rs758372103	snp	C/T	3.29462e-05	0.00405857	missense	RNF213	GRCh38.p7	17:80290572	GGTTTTCCACCAGCA[C/T]GCTGAGCCCGGGTGG	57674
rs758384014	snp	A/G	3.295e-05	0.00405881	missense	RNF213	GRCh38.p7	17:80307177	TAGAAATGCTGTTGC[A/G]ACTCCTGGACACTTA	57674
rs758385481	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80261956	CGGGAGGCGGAGGTT[-/G]CAGTGAGCTGAGATT	57674
rs758404728	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357159	TGACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC	57674
rs758410619	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370779	ACCCGTGCTGGGAGG[A/G]AGGATGCACATGATA	57674
rs758429795	snp	C/T	1.65239e-05	0.00287431	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380973	CTGCTTCTGGGAGCG[C/T]CCCAGAGTTCCCAGG	57674
rs758450439	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80284613	CACCTTTCTAATCCC[A/G]TTGAGGAAGTTTATT	57674
rs758454091	snp	C/T	0.000119012	0.0077131	missense	RNF213	GRCh38.p7	17:80339825	TCTCCCGTGGAGCGT[C/T]GTCTCCCGAGAGGTC	57674
rs758464578	snp	C/T	4.94181e-05	0.00497057	synonymous-codon	RNF213	GRCh38.p7	17:80346198	AGAAGTCCTCTGCGC[C/T]TCTCAGGGTTTCATG	57674
rs758471398	snp	G/T	1.64855e-05	0.00287097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381496	ACCAGGCTCACCATC[G/T]TCTCTACAAACCAGA	57674
rs758480939	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362814	AAATTAAAGTATGGC[C/T]GTATGATGGGTTATT	57674
rs758486038	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326383	ATCTATCTCTGCCAC[C/T]ATCACACGGGCAGTA	57674
rs758486635	snp	A/G	1.66774e-05	0.00288763	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372641	CGAGAGCCTGCCAAC[A/G]AGGCCTCGGTTGAAT	57674
rs758488123	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80266347	TGAGCCTGGGAAGTC[A/G]AGGCTGCAGTAAGCC	57674
rs758488371	snp	A/T	3.29473e-05	0.00405864	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367800	CTTTTGAGGCCGTGA[A/T]GCGCACTCTCTGTGA	57674
rs758490477	snp	A/T	0.000114162	0.00755433	missense	RNF213	GRCh38.p7	17:80327957	AGCTGATTATAAAGC[A/T]CAAGAATCAGTTTCT	57674
rs758495079	snp	C/G	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389924	CTGCACAAAGTAAGT[C/G]TGGTCTCTTCCTCTC	57674
rs758503579	snp	C/T	3.7428e-05	0.0043258	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351675	TATTCTTTTTTTTTT[C/T]TTTAAATAGGTATTC	57674
rs758517695	snp	C/T	1.70682e-05	0.00292127	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363579	TGGGAGGGGCACCGC[C/T]CAGCCACGCCCTGCT	57674
rs758521972	snp	C/T	1.65105e-05	0.00287315	intron-variant	RNF213	GRCh38.p7	17:80313180	GAGGTAGGCATTTGG[C/T]CGAAGGCTTCTGGGT	57674
rs758526654	snp	A/C/G	3.29501e-05	0.00405884	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385163	GCTTCCTCAGCAAGC[A/C/G]CAGCTCAGGTGTGGC	57674
rs758532913	snp	C/T	1.68295e-05	0.00290077	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354177	CCACGGTATGAGCCT[C/T]CCCACCCCTCTTGCC	57674
rs758560639	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268298	GGTCAACGCTGCAGT[A/G]AGCCGTGATCATACC	57674
rs758579309	snp	C/T	0.00015387	0.00876991	synonymous-codon	RNF213	GRCh38.p7	17:80340055	CTACAGCCTGCTGTT[C/T]GCAGATCAGCTGAGC	57674
rs758594070	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80295467	ACGGAATGGGGTCTG[C/T]TGCCCTAGCTGTGGT	57674
rs758600643	snp	A/G	1.64836e-05	0.0028708	missense	RNF213	GRCh38.p7	17:80347747	CTGGGGACCCACCGC[A/G]TCAAATGTCGGGTTC	57674
rs758624450	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80306851	AGCGAGACTCCATCT[-/C]AAAAAAAAAAAAAAA	57674
rs758649873	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80306304	TTGCTGAGCATAGAC[A/G]AGCCTCTCTTCCGGT	57674
rs758655706	snp	A/G	3.41997e-05	0.00413506	splice-donor-variant	RNF213	GRCh38.p7	17:80350397	CATTGCCTCAGCTAA[A/G]TATGTTTTTAGTATT	57674
rs758664381	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	RNF213	GRCh38.p7	17:80345742	CAGGGAGGCTGAAAA[C/T]GTGGCCTTCGCCAAT	57674
rs758667908	snp	A/T	1.65745e-05	0.00287871	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363305	CCATGAGCTGGCTGG[A/T]TGTGAGATGGTATGG	57674
rs758680846	snp	C/G	0.00011698	0.00764697	intron-variant	RNF213	GRCh38.p7	17:80337581	CTCTCCTTTTGTCCC[C/G]ATAGTGTGACTCCGC	57674
rs758683996	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294565	GAGGAGTCTGGCTGT[C/T]GTCAGTGTGTGGGTT	57674
rs758689243	snp	A/G	3.29587e-05	0.00405934	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376480	TGCAGCCGTCCTTCT[A/G]TGTGGACAGAATGAA	57674
rs758691873	snp	G/T	3.9571e-05	0.00444792	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288090	GCAGGCCCAGGCTTT[G/T]GGAGAGGCAGGAGTG	57674
rs758692663	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80335702	CAGTACAGGCTGGGC[A/G]TGGTGGCTCACACCT	57674
rs758696622	in-del	-/T	1.65127e-05	0.00287334	frameshift-variant	RNF213	GRCh38.p7	17:80347402	ATCAAACAGAACATC[-/T]TTGGGCCTTCTCAGA	57674
rs758714165	snp	A/C	1.67626e-05	0.002895	intron-variant	RNF213	GRCh38.p7	17:80291857	CAGGCTGTCTGCTCA[A/C]CCCTCCGGAGTGCAG	57674
rs758715125	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268895	GGAAAGAAAGAAGCC[A/G]GTAGTTGCTCAGTCT	57674
rs758716546	snp	C/T	3.29468e-05	0.00405861	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367938	TCTCTGCTTCAGAAC[C/T]GATTGCCCTTCTTGG	57674
rs758723405	snp	A/G	3.30376e-05	0.0040642	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386660	CGCATGCCTGGCCTG[A/G]ACGCTGAGCGCTGTC	57674
rs758730525	snp	A/G	3.29457e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383798	TGCCCCACCTGCCCC[A/G]GAAAAGTGTGGTCCA	57674
rs758731942	snp	G/T	1.64985e-05	0.0028721	missense	RNF213	GRCh38.p7	17:80347862	AGCACTATCTGGATA[G/T]CAACACGGTGCTGGA	57674
rs758746223	snp	G/T	1.64827e-05	0.00287073	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358449	GTGACACGATGCTTC[G/T]GAACATTCCTCTTGT	57674
rs758749638	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267320	GTGGCGTGTACCTGT[A/G]GTCCCAGCTACTCGG	57674
rs758763021	snp	C/T	9.97034e-05	0.00705987	intron-variant	RNF213	GRCh38.p7	17:80343369	CCACATCAGTAAAGA[C/T]GTGGTCCCCATGTCT	57674
rs758766027	snp	C/G/T	3.29871e-05	0.00406112	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386714	GGATGCCGCCGAGGT[C/G/T]ACTGAACTGCATGTC	57674
rs758777063	snp	A/C	1.70336e-05	0.00291831	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373146	AGTGGGTGTTTCCCA[A/C]GGACGTTGTCAAGCA	57674
rs758782436	snp	A/C	1.69203e-05	0.00290859	missense	RNF213	GRCh38.p7	17:80347274	CCCCGCAAGACATTG[A/C]ACAGGCTGTCCTTAG	57674
rs758808914	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320233	AATTGCTGAACATAA[A/G]CAACTGCTTCTGTGG	57674
rs758812497	snp	A/C/T	4.96474e-05	0.00498213	synonymous-codon, missense	RNF213	GRCh38.p7	17:80346802	ATCATCAGCACCTTC[A/C/T]GGCAGTGCGCCCGCT	57674
rs758814638	snp	C/G	1.64827e-05	0.00287073	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383710	CCCACCATGAATAAT[C/G]TCATCAGCCAAGATA	57674
rs758818414	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382787	GAATTTTTAGAGATT[A/G]ATGTTATCTTCAAAA	57674
rs758827271	snp	G/T	1.66349e-05	0.00288395	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369892	ACATGGAGACTTGCT[G/T]CTGGAAAGCCCTGGC	57674
rs758850644	snp	A/G	1.6513e-05	0.00287336	synonymous-codon	RNF213	GRCh38.p7	17:80348262	GCACACGGCAGACCT[A/G]GAGCGCCACGCCATC	57674
rs758853515	snp	C/T	6.59598e-05	0.00574243	intron-variant	RNF213	GRCh38.p7	17:80306217	TCACTGATCTCACTG[C/T]GTCTCTTTTCTCCGT	57674
rs758857802	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392348	CCAGTCTTTGTTAAT[A/G]TGAAACATGTAATAG	57674
rs758883572	snp	A/G	1.65321e-05	0.00287502	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353583	AGCACATCAGGGGAG[A/G]TGGCAGAGGTGGCAG	57674
rs758888868	in-del	-/TTGTG	1.66051e-05	0.00288137	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376538	TCTCCCCAGCCACCA[-/TTGTG]TGGCGGTAAGAGTAG	57674
rs758889108	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80285867	GTAGAGATGGGGAGG[-/A]ATCTCACCATGTTGG	57674
rs758896947	snp	A/G	1.67598e-05	0.00289476	missense	RNF213	GRCh38.p7	17:80346688	ACCATCGTGGCAGAC[A/G]CCATGCAGGGCCCGG	57674
rs758897646	snp	A/G	6.72891e-05	0.0058	intron-variant	RNF213	GRCh38.p7	17:80289624	GAAAATGTGGAGGCC[A/G]GCCTTCAAGGTCAGG	57674
rs758903949	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80276549	ACCGACATGAACAAG[A/C]GAACAATAAAAGAGG	57674
rs758913142	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357699	TAAAGCAGATAAGTG[C/T]GGTGGCTCACACCTG	57674
rs758918116	snp	A/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80294830	GTGAAGGGGAAGCAG[A/T]TTGCCGCTGCGCTCA	57674
rs758919299	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259209	GCAGTGGCTCATGCC[C/T]GTAATTCCAGCACTT	57674
rs758934124	snp	A/G	6.59467e-05	0.00574187	synonymous-codon	RNF213	GRCh38.p7	17:80345811	TGAAGCCAACACAAC[A/G]GAAGCTATAAGCTGT	57674
rs758937818	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283559	CCCGGGCTCTGCCCA[A/G]CCTCCGTGTGCTGCT	57674
rs758941357	snp	A/G	1.64846e-05	0.0028709	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364463	GATTTTCTCCACCGC[A/G]CTCTTCGTGGAGCAC	57674
rs758941475	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80314474	GGTGGTGATGGTGAT[C/G]GTGGAGGTACTGGAG	57674
rs758970700	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80345275	AATGACGACCACACA[A/G]CCATGACATTCATCG	57674
rs758976320	snp	A/G	1.69859e-05	0.00291421	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358520	GGGAGAGAAACTATC[A/G]GAACACAGCAGGACC	57674
rs758980633	snp	C/T	1.64743e-05	0.00287	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376456	GGTGACAGAAATGGC[C/T]ATTCATGCTGCAGCC	57674
rs758994318	snp	A/G	3.30136e-05	0.00406273	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369743	TGTCTCATGCAGTGA[A/G]CTGCCTTTTTCTTTC	57674
rs758999569	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366702	AAATGTCATCAGTTA[C/T]ATAAATTAAAAGATA	57674
rs759015333	snp	A/G	1.64803e-05	0.00287052	missense	RNF213	GRCh38.p7	17:80347720	GGCGGCCAGAAGTAC[A/G]TGGACCTCGGTCTGG	57674
rs759019499	snp	C/T	2.31463e-05	0.00340185	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288066	CACCGAGGTTGGCGA[C/T]AGCCCCCTGCAGGCC	57674
rs759019852	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356529	ACCTCGATTCACCAC[C/T]ACTGTGTTCTGGGGA	57674
rs759025644	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80283946	CTTTGGGTAATGGCC[A/G]GGCACAGTGGCTCAC	57674
rs759036251	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277971	CACAGAGAGGGGCCC[A/G]CGCCTGTCCCTTGGC	57674
rs759045429	snp	C/G	4.98426e-05	0.00499187	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376541	TCCCCAGCCACCATG[C/G]CGGTAAGAGTAGGCC	57674
rs759047123	in-del	-/A	1.64773e-05	0.00287026	frameshift-variant	RNF213	GRCh38.p7	17:80346103	TGAGTGACGTTGCTG[-/A]AAAAGCTCTACATCC	57674
rs759063546	in-del	-/T	1.90035e-05	0.00308243	intron-variant	RNF213	GRCh38.p7	17:80350253	GAATTTTCTTTTCCA[-/T]TTTTTTAAGACAGAG	57674
rs759067895	snp	C/T	1.6795e-05	0.0028978	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386477	TGCTCAGCCCAGAGT[C/T]CCTAAGCCCAGTGGG	57674
rs759070783	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362418	TAAAACAACAATTTT[A/G]TAATCTCATTAAGCA	57674
rs759078459	snp	C/T	1.64893e-05	0.0028713	synonymous-codon	RNF213	GRCh38.p7	17:80347815	CGTCGTGTACAAACA[C/T]TTTCCCATCCCCCTC	57674
rs759090946	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80336470	AAATGGTGGCACACC[C/T]GTGTGGTAGGTTTGT	57674
rs759092504	snp	G/T	1.6478e-05	0.00287032	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381537	ACACTCTGTTCCGTT[G/T]CCCCCACAGGCTCTG	57674
rs759103836	snp	C/T	4.30246e-05	0.00463794	intron-variant	RNF213	GRCh38.p7	17:80343341	GTAAGTGCCCTCCAG[C/T]GTCAGCCGATGGCCA	57674
rs759104395	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397916	ATGGATCCTGAGAGC[A/G]CTCTCAGGCAGGCAA	57674
rs759136816	snp	C/T	3.33985e-05	0.00408633	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358497	GAGTGGAAGGCTTTC[C/T]TTCCCTGGGGAGAGA	57674
rs759162874	snp	G/T	2.62488e-05	0.00362267	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351640	CTTGTTTTTGTGTGT[G/T]TGTTTGTTTTTAAAA	57674
rs759181175	snp	A/G	1.64974e-05	0.00287201	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386700	CTCAGCTATTCCGTG[A/G]ATGCCGCCGAGGTCA	57674
rs759184989	in-del	-/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383650	ACCTCACTTCCAGAA[-/T]TTTTTTTTTTCATTT	57674
rs759191353	snp	A/C	1.64836e-05	0.0028708	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364454	GTGGAGTCGGATTTT[A/C]TCCACCGCACTCTTC	57674
rs759205883	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80324889	TGTAAAGTGTTTTAC[A/T]ATTTTGCTCTTTTTG	57674
rs759211824	snp	A/G	6.59033e-05	0.00573997	missense	RNF213	GRCh38.p7	17:80294740	CATCAGTACTATGAC[A/G]TAGTTTATATGAAGC	57674
rs759256018	snp	C/T	1.64781e-05	0.00287033	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374464	GTATTCCAGGGGCTG[C/T]GGCAGGACCACCCAG	57674
rs759257351	snp	G/T	1.65277e-05	0.00287464	missense	RNF213	GRCh38.p7	17:80346862	GTCTCTGTGGTGGTG[G/T]TAGATGAGGTGGGGC	57674
rs759264860	snp	A/G	5.12869e-05	0.00506368	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288153	ATTCCAGGACCACAC[A/G]GAAGGGGAGGACCAG	57674
rs759265439	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383771	TAATATATGGTGACC[C/T]AGTGACCTTCCTGCC	57674
rs759267469	in-del	-/CT	9.90827e-05	0.00703786	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380801	GCGGCCAGCCTCAGC[-/CT]CTGTCTTGTGTTCTC	57674
rs759274197	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80292653	CGCAGAGCCCTCTGC[A/G]CCCCTTCATGCCTCT	57674
rs759279121	snp	C/T			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321836	GTTCAAGCAATTCTC[C/T]TGCCTCAGTCTCTCG	57674
rs759280054	snp	A/G	9.88468e-05	0.00702948	missense	RNF213	GRCh38.p7	17:80307186	TGTTGCGACTCCTGG[A/G]CACTTACCGGGACAA	57674
rs759300901	snp	A/G	1.64732e-05	0.0028699	intron-variant	RNF213	GRCh38.p7	17:80343826	TCGCCATCGTGTCGT[A/G]TGTTTACACCTCGTG	57674
rs759301599	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80335159	AACTCCTGACCTCAG[A/G]TGATCCACCCATCTC	57674
rs759311073	snp	A/G	1.90747e-05	0.0030882	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373185	GAAGCGGGGCCGGGC[A/G]GCACACAAACATGCA	57674
rs759312431	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80265681	CTGTAGCCACAGGGT[A/T]GAAATTGTAGAAAAT	57674
rs759314994	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80344899	TCAGTATCAAGAAGG[C/T]TCTGTCGAAGGCACC	57674
rs759315069	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	RNF213	GRCh38.p7	17:80345931	CCGGAAGCACTCTGA[A/G]GAGATGATCTGCCGT	57674
rs759335062	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	RNF213	GRCh38.p7	17:80345778	CCAACATCAGTTGGA[C/T]ACCATCTTGTTTTTT	57674
rs759348562	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266865	CTTGAGGAAGGCATG[C/T]TGAAAGCTGAGATAG	57674
rs759352731	snp	C/T	1.65567e-05	0.00287716	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393543	TTTGGAGAGAAGACT[C/T]CTCTCTCCTCGTCTG	57674
rs759370077	in-del	-/AT			intron-variant	RNF213	GRCh38.p7	17:80331291	ATGTTACCAGGCCTC[-/AT]GTGTCATTTACCACT	57674
rs759389448	snp	A/G			missense	RNF213	GRCh38.p7	17:80346847	GACCTGCAGCAGTAC[A/G]TCTCTGTGGTGGTGT	57674
rs759399580	snp	C/T	1.6476e-05	0.00287014	intron-variant, missense	RNF213	GRCh38.p7	17:80319328	GTGAACAATCTCTCC[C/T]CCTGGGAAACGGATT	57674
rs759416105	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319984	AGTGACTGATACCTT[C/T]GATAAGGTTTTCCTT	57674
rs759441593	snp	A/G	1.65192e-05	0.00287391	missense	RNF213	GRCh38.p7	17:80295812	CTTGGGATACCTCAG[A/G]GGTATTATTATTTTT	57674
rs759442148	snp	A/G/T	0.000125201	0.00791115	intron-variant	RNF213	GRCh38.p7	17:80289615	AAAAAAAAAGAAAAT[A/G/T]TGGAGGCCGGCCTTC	57674
rs759448743	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80349811	AAGTCACGACTGTGA[A/G]ATTTTAGAATCAGAG	57674
rs759455900	snp	G/T	1.64808e-05	0.00287057	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376280	TTGATACATCTTAAT[G/T]TTAAGTTTTTTTCCT	57674
rs759463576	snp	A/C	1.64754e-05	0.00287009	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372955	CCAGCCACTCACCCG[A/C]TTTCTCGTTGGCCTC	57674
rs759475828	snp	A/G	6.25489e-05	0.005592	intron-variant	RNF213	GRCh38.p7	17:80340395	AGGCCCCGTCTCCCA[A/G]GGACTGCCCGGGGCC	57674
rs759477111	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287799	AAATAAAGTGAGTGT[C/T]TCTCTTTCTGTTTAG	57674
rs759477948	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397897	TCCAGCCAGCTTGAG[C/T]GACATGGATCCTGAG	57674
rs759485797	snp	C/G	4.94189e-05	0.00497062	missense	RNF213	GRCh38.p7	17:80309130	CTGCCAGCCTTATCT[C/G]CCGAGATTGTCTGCA	57674
rs759486964	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391883	TCAAGCGATTCTCCT[C/G]CCTCAGCCTCCCGAG	57674
rs759491056	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382377	TGACCATTGTGAGGA[A/C]AATGTTAATTTAAAA	57674
rs759503959	snp	A/G	1.71905e-05	0.00293172	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372735	CTGAGGGAGGCCCAG[A/G]CAAGTCTTCTCTGCC	57674
rs759506607	snp	C/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80258843	TGAGCAGCACTCCGG[C/T]CCAGCACTATTACGT	57674
rs759508808	snp	A/G	3.30087e-05	0.00406242	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380820	GTCTTGTGTTCTCTC[A/G]TTCTTTCCAGAGACA	57674
rs759509360	snp	C/T	1.65784e-05	0.00287905	synonymous-codon	RNF213	GRCh38.p7	17:80347353	CAATTTGCCCGAGGC[C/T]AAGTGCTCAGAGGAA	57674
rs759511123	snp	A/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80344948	CATTTCCTGTTTCAC[A/T]GCGGGGTAATAAACC	57674
rs759511226	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366142	TTGGGGGAAAGCCCT[A/G]CCTTCCGCCGTGAGG	57674
rs759559424	snp	A/G	6.59642e-05	0.00574262	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389304	TGGGGATCCAAACAT[A/G]CAGCTGAATGTGTAT	57674
rs759562976	in-del	-/CT	1.65323e-05	0.00287505	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383957	ACTGTGGCTCCCTCC[-/CT]CTTTCGGTGCAGAGT	57674
rs759564918	snp	C/T	0.000114227	0.00755648	intron-variant, missense	RNF213	GRCh38.p7	17:80278780	GAGCTACATCAGAGG[C/T]TTTGGTAGATGCTGC	57674
rs759569424	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362991	ACAGAATAGCACACA[C/T]GGTTTCTAATTTCCT	57674
rs759570290	snp	C/T	1.64988e-05	0.00287213	synonymous-codon	RNF213	GRCh38.p7	17:80290723	CTGTGAGCTGCACTA[C/T]ACCAGGTGAGCGTGT	57674
rs759575167	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390956	AGTCCCACCTACTCA[A/G]GAGGCTGAGGCAGGA	57674
rs759579633	snp	C/T	3.30458e-05	0.0040647	intron-variant, missense	RNF213	GRCh38.p7	17:80319451	TGGGCACCCTCCTCC[C/T]TCGCCAAGGGCAATG	57674
rs759583595	snp	A/G	3.29473e-05	0.00405864	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389217	CATCAGTGGACAGCT[A/G]CAGTCCTACAGCGAT	57674
rs759596647	snp	A/G/T	6.60977e-05	0.0057485	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363137	GTCCTGCACTAGGAA[A/G/T]CTGAAAGCGGCGTCA	57674
rs759600894	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365488	ACCCCGTGGCCTGGC[A/G]TCACAGCCTGTGGGA	57674
rs759645157	in-del	-/GT/T			intron-variant	RNF213	GRCh38.p7	17:80313471	GTAGAGGTGATGGTG[-/GT/T]GTGGAGGTGATGGTG	57674
rs759656834	snp	A/G			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288497	CCCTGGGTGGGAGTC[A/G]GAGGGCTGCCCCTCC	57674
rs759660765	snp	G/T	1.65605e-05	0.0028775	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386289	ACTGCAGCACTGACT[G/T]GGATCTGGACACTGA	57674
rs759661028	snp	C/T	5.01341e-05	0.00500645	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381681	CGGCGTGGTCCACCT[C/T]GTCCTGCGCAGGCTT	57674
rs759673904	snp	C/G	3.39225e-05	0.00411826	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288254	AAGGCCATTCTAGGA[C/G]TGAAGATGCTGCCCA	57674
rs759674177	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377972	GCTAAGGGTTTCTAG[C/T]CCAGGGCTTCTCAGA	57674
rs759686715	snp	A/G	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390094	GCACATTCCTAAATC[A/G]GACTGGCCTAGACGC	57674
rs759687678	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328208	AAAAAGTGGGTATGC[A/G]CAAAACCATCCTAGT	57674
rs759692190	snp	C/T	3.40971e-05	0.00412885	synonymous-codon	RNF213	GRCh38.p7	17:80340301	CCTGTCGGCGGCAGC[C/T]GTGTTCAATGACCGG	57674
rs759705575	snp	A/G	1.64955e-05	0.00287184	synonymous-codon	RNF213	GRCh38.p7	17:80347461	TGAGTCCCGCTACTT[A/G]CTCGTGCTGACCAAA	57674
rs759712166	snp	C/G			missense	RNF213	GRCh38.p7	17:80339819	GGTGGGTCTCCCGTG[C/G]AGCGTTGTCTCCCGA	57674
rs759713985	snp	A/G	1.75194e-05	0.00295963	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385648	GTCCCCTGTACCACT[A/G]AGCGTTCCAGGAGAG	57674
rs759725442	in-del	-/AAT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375555	AAGAAAAAAAAAAAG[-/AAT]TAGCCGGACATGGTT	57674
rs759726740	snp	C/T	0.000313389	0.0125138	synonymous-codon	RNF213	GRCh38.p7	17:80345514	CCCCGACAAAACGTA[C/T]GAGCTCACAACCGAC	57674
rs759743347	snp	A/T	0.000117973	0.00767937	missense	RNF213	GRCh38.p7	17:80332549	TGCACCAGGCTGTCC[A/T]CGCAGCCAAGGTCAT	57674
rs759752387	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352579	TGAATAATTTCGTGG[A/C]GAATGGAAGGCAGAC	57674
rs759763506	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80310142	TCTGAGCTCTGTCTG[C/T]GTGGTGCAGAGATCG	57674
rs759766560	snp	A/G	6.59163e-05	0.00574054	intron-variant	RNF213	GRCh38.p7	17:80291609	TTTGGATAGCCAACC[A/G]TATCCTGTTCATTCA	57674
rs759772490	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80269788	TCCATGTATCTACCT[A/G]TCTACCTGTCTACCT	57674
rs759780722	snp	A/G	3.32945e-05	0.00407997	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375714	TCTCAAAAAAAAAAG[A/G]TGTGTTGAGCTTTTA	57674
rs759782016	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80280552	TTGACTTCCTGGGCT[C/G]AAGCAATCCTCGTGC	57674
rs759791920	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385373	AAAAGCACCTCCCTC[C/T]CTAGCTCCTCAAACT	57674
rs759802885	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80338380	TAACTAAGATTTAGA[C/T]GGACAAAACAGAAGT	57674
rs759829243	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386325	AGATCCTCTTGCCAC[A/G]CCGACGGGGCCTGGG	57674
rs759830053	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360319	AATTTTGGAGTTTTT[A/G]GTTTTCACACTTTGT	57674
rs759834289	snp	A/T	9.00779e-05	0.0067105	missense	RNF213	GRCh38.p7	17:80339348	GGCTTGGACCTGGTG[A/T]CGGAGCTTAAAGAAG	57674
rs759860829	snp	A/G	2.05548e-05	0.00320577	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386879	CCAGGGCAAGCCCCG[A/G]CTGAGCCTCAAGGTA	57674
rs759864085	snp	C/G	3.32651e-05	0.00407817	intron-variant	RNF213	GRCh38.p7	17:80273208	CACTCGCTTCTCTCT[C/G]AGATCTGACCCTTCC	57674
rs759872559	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394289	AACTTGGTCACAGGC[C/G]TGGTTCTGGCAGTTC	57674
rs759887716	snp	C/G	0.000166395	0.00911975	intron-variant	RNF213	GRCh38.p7	17:80344047	GTTTTCGCCTGGCGT[C/G]GGGGGCTCTTGGGTT	57674
rs759888992	snp	A/G	1.65151e-05	0.00287355	missense	RNF213	GRCh38.p7	17:80348119	ATCCTGCTGAACTGC[A/G]CTACGCCCGATGCCG	57674
rs759901778	snp	A/T	1.66754e-05	0.00288746	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374588	TTAAGACTGCTCTGA[A/T]GGTAGGATGGGCCCG	57674
rs759902605	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293640	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	57674
rs759915787	snp	G/T	1.68892e-05	0.00290591	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386840	TCTGGAGAAGATTCA[G/T]CGGCAGATCGTCAGC	57674
rs759915902	snp	A/C	8.28041e-05	0.00643391	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390156	TTGAAACTAAAGAAC[A/C]CCCAAACCCAAACCG	57674
rs759917499	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370227	CTTAGAATCCTGCTC[A/G]CCCTGAATGTCCTAG	57674
rs759943553	snp	C/T	6.93854e-05	0.00588964	intron-variant	RNF213	GRCh38.p7	17:80306484	GTTTGTGTCTGAAGT[C/T]GGCTCTGGAGTCCTG	57674
rs759945544	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394742	GCGCCGGCAGGAGGC[A/T]CGGAAGGAACTGTGC	57674
rs759955344	snp	C/T	1.81612e-05	0.00301335	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376977	CAGTAAGTGTTGGGG[C/T]CTAGATGACCCCACA	57674
rs759958425	snp	C/G	1.66546e-05	0.00288566	missense	RNF213	GRCh38.p7	17:80295557	TTCTCCCACCATCAG[C/G]TGAAGAGATACCTGT	57674
rs759971806	in-del	-/CC	1.71035e-05	0.00292429	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363575	CCGGTGGGAGGGGCA[-/CC]GCTCAGCCACGCCCT	57674
rs759992042	snp	C/T	6.91838e-05	0.00588108	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288374	CTATGGTGAGTCATC[C/T]GGGAGAGATGGCCTG	57674
rs759992177	snp	A/C/T	3.30749e-05	0.00406652	missense	RNF213	GRCh38.p7	17:80348024	CCTGCGCGTCTGTGG[A/C/T]GCTGCAGGTCATAGA	57674
rs760000273	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80279762	ACGTGAGCCACTGTG[C/G]CTGCCCCAAATCCTG	57674
rs760007056	snp	G/T	3.53263e-05	0.00420261	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374704	GATGCAGCCCATCAC[G/T]TGACACTGTATTGGA	57674
rs760014106	snp	A/G	0.000234714	0.0108306	synonymous-codon	RNF213	GRCh38.p7	17:80332217	GGAAGCCGCAGAGCC[A/G]CTGAGTGAGCCTAAG	57674
rs760015677	snp	C/T	1.65696e-05	0.00287828	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385014	GTAAATAAAAATTGT[C/T]ACTGGGTGGTCTTCC	57674
rs760032181	snp	A/C	1.68496e-05	0.0029025	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372033	TGGAAACTATCTGAA[A/C]CACATGGTTTAAAAT	57674
rs760048325	snp	A/G	0.000114989	0.00758163	intron-variant	RNF213	GRCh38.p7	17:80337801	GGTCTTCTGGCCCCA[A/G]GAAAGTGACTTCTAA	57674
rs760049185	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359328	CCCAGGGGTTGAAGA[A/C]CAGCTTGGGCAACAT	57674
rs760068027	snp	A/G	6.65458e-05	0.00576788	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361699	CGCCATGACTTAGAC[A/G]CACTCCAGGCCGCTC	57674
rs760071805	snp	A/G	2.20242e-05	0.00331838	missense	RNF213	GRCh38.p7	17:80289824	GAAGCAGATGTCCAG[A/G]AAGTGAAGGCAAGGT	57674
rs760072187	snp	A/C	1.64776e-05	0.00287028	missense	RNF213	GRCh38.p7	17:80346088	TGGGACTTTGGACAA[A/C]TGAGTGACGTTGCTG	57674
rs760076600	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80262972	CCCTGAGGCTTCTTA[A/C]TGGGGAGGGAGAGAG	57674
rs760081382	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381318	CACTGCATAACCAAG[A/G]TGGCCAACAGTACAA	57674
rs760082524	in-del	-/GTGTGCTTGTGTGTGTGCGTGTGT			intron-variant	RNF213	GRCh38.p7	17:80290397	CGTGTGTGCGTGTAC[-/GTGTGCTTGTGTGTGTGCGTGTGT]GCGAGTGTGCGCGTG	57674
rs760114367	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80263889	AGCTCAGGTGGGGCC[A/G]AGGTCCTCTGTGGCT	57674
rs760116718	snp	C/T	1.66349e-05	0.00288395	missense	RNF213	GRCh38.p7	17:80273271	ACTCCACAATGGCGT[C/T]GGCCTCGGAGGGTGA	57674
rs760117021	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80302791	CTTGAGCCAGGGAGG[A/T]CAAGGCTGCAGTGGT	57674
rs760127427	snp	A/C	1.83761e-05	0.00303112	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360183	AGCTGTGGGTCCAGG[A/C]TCAGTACATCACAGA	57674
rs760128593	snp	C/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80306394	CACCTGGGTCGTTTT[C/T]CTGCTCATATCCTGG	57674
rs760131920	snp	C/T	6.58903e-05	0.00573941	intron-variant	RNF213	GRCh38.p7	17:80343838	CGTGTGTTTACACCT[C/T]GTGCGATTCTGTTCT	57674
rs760137580	snp	A/G	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80307146	GTTCAGGATGTTCAG[A/G]ACGTTCAGAACATTT	57674
rs760138653	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80294796	GAACCACATCACAGA[C/T]GGGCCGAGGAAGGAC	57674
rs760143212	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281917	GCTGGAGTGCAATGG[C/T]GTGATCTCGGCTCCC	57674
rs760156655	snp	C/T	1.66078e-05	0.00288161	synonymous-codon	RNF213	GRCh38.p7	17:80346774	GTGCAGCCCGCACTC[C/T]ACCCCACAGGGCATC	57674
rs760160785	in-del	-/TGGAGGTGA			intron-variant	RNF213	GRCh38.p7	17:80313828	AGGTGATGGTGGTGG[-/TGGAGGTGA]TGGTGGAGGTACTGG	57674
rs760160793	snp	A/G	4.95724e-05	0.00497833	missense	RNF213	GRCh38.p7	17:80263745	TTCTGCAGCCAGTGC[A/G]GAGAGAGGCTGCCTC	57674
rs760169991	snp	A/G	0.000131781	0.00811621	missense	RNF213	GRCh38.p7	17:80343939	GGAAAATGTGGCTTC[A/G]GAACCCCTGCCATTT	57674
rs760177242	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380633	TGACGCTGAGAATGC[A/G]GTCGGGTCTGGTCCA	57674
rs760198453	snp	A/G	3.31285e-05	0.00406978	synonymous-codon	RNF213	GRCh38.p7	17:80346885	GGTGGGGCTGGCGGA[A/G]GACTCACCCAAAATG	57674
rs760204301	snp	A/T	1.71185e-05	0.00292557	intron-variant	RNF213	GRCh38.p7	17:80263827	AGTGGGGACCCCTGG[A/T]GATGTCTCACCTCCC	57674
rs760232317	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80327065	TGTTTCTCTCTTTGC[A/T]TATGCTATGAAAGTG	57674
rs760235173	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354385	GGGACAGAAGCACTC[C/T]GGAGCCAACAGCTCA	57674
rs760244884	snp	A/G	1.67888e-05	0.00289726	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358507	CTTTCTTTCCCTGGG[A/G]AGAGAAACTATCAGA	57674
rs760249870	in-del	-/GTGTGCATGTAT			intron-variant	RNF213	GRCh38.p7	17:80290347	TGCGCACGTGTGTGC[-/GTGTGCATGTAT]GTGTGCGTGTGTGAG	57674
rs760259464	snp	A/G	1.64749e-05	0.00287005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390069	AGCCCGGAAAATGCT[A/G]AGCTCCTCAGCACAT	57674
rs760262655	in-del	-/ACTC			intron-variant	RNF213	GRCh38.p7	17:80281702	TCACACCCATCTCAT[-/ACTC]ACTCACACTGAAACA	57674
rs760267891	in-del	-/TCCA			intron-variant	RNF213	GRCh38.p7	17:80269764	TTATCTATCCATCCG[-/TCCA]TCCATCCATCCATGT	57674
rs760284930	snp	A/G	1.64958e-05	0.00287187	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386706	TATTCCGTGGATGCC[A/G]CCGAGGTCACTGAAC	57674
rs760298667	snp	C/T	3.33317e-05	0.00408224	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363648	GCCTGCACGGAGATG[C/T]TGACAAGAAACACCC	57674
rs760302927	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317487	AGGACAGAGAAGAAC[A/G]AGGGCCCAGGATCTC	57674
rs760313419	snp	C/T	1.6517e-05	0.00287372	synonymous-codon	RNF213	GRCh38.p7	17:80347932	GGTGGAGAAGTTCAT[C/T]AATGTCAAAGCACAT	57674
rs760322219	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337262	AGAATGATGGCGTCT[A/G]GTAGAGAGGCAGGCG	57674
rs760322802	snp	C/G	1.64743e-05	0.00287	synonymous-codon	RNF213	GRCh38.p7	17:80294886	GCAGACCTGGGACAC[C/G]ATCAACCTGAACAGC	57674
rs760322886	snp	C/T	3.29511e-05	0.00405887	missense	RNF213	GRCh38.p7	17:80345944	GAGGAGATGATCTGC[C/T]GTTTGGAGTCAGCTG	57674
rs760326590	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80284998	AGTAAGGCTGATGTT[A/C]CTCAAACCATGCAGC	57674
rs760327156	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80263384	CCCCTATCCCCACCC[-/A]GCCCAACCCATGTTC	57674
rs760330653	snp	A/G	1.66275e-05	0.00288331	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353563	AGGCGATGGAGACGG[A/G]GGCCAGCACATCAGG	57674
rs760343069	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385838	GCAATTCTCCTGCCT[C/T]AGCCCCTAGTAGAGA	57674
rs760355065	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388351	ACCTGTTGCCCTAGC[A/G]CCTCCTGTGGCGAAG	57674
rs760384798	snp	C/T	3.30518e-05	0.00406507	intron-variant, missense	RNF213	GRCh38.p7	17:80319455	CACCCTCCTCCCTCG[C/T]CAAGGGCAATGGCGC	57674
rs760391468	snp	A/G	3.29587e-05	0.00405934	missense	RNF213	GRCh38.p7	17:80346056	ATGCTCTGCCCCCGA[A/G]CCTGATTCCTCTGGT	57674
rs760397781	in-del	-/GCACACCCTCTCCCT			intron-variant	RNF213	GRCh38.p7	17:80289886	CTGCCTGAGAGCCCG[-/GCACACCCTCTCCCT]GCACACCCTCTCCCT	57674
rs760402595	snp	C/G	1.65949e-05	0.00288048	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369847	CCGCTCAGTGATACT[C/G]AAACTGCTTTTGAAG	57674
rs760412743	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80295122	GAATGTGTAGAACTT[G/T]CCAGCCTTTTCTCCT	57674
rs760420078	snp	A/G	6.58903e-05	0.00573941	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389233	CAGTCCTACAGCGAT[A/G]CCTGTGAAGTGCTGT	57674
rs760432544	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80349831	TAGAATCAGAGGTCA[C/T]AGGCAGGGCTCCGAA	57674
rs760444991	snp	C/T	8.25621e-05	0.0064245	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389322	GCTGAATGTGTATAC[C/T]CAAGACATCCTGCAA	57674
rs760445394	snp	A/G	3.29457e-05	0.00405854	missense	RNF213	GRCh38.p7	17:80345078	CACTGAGGGGCTTCA[A/G]GAAGTTCGTGGTGAC	57674
rs760447645	snp	C/T	9.33402e-05	0.00683091	intron-variant	RNF213	GRCh38.p7	17:80339198	ATGGTTCTGCCTCTC[C/T]AGGTCTTCTGCAGTG	57674
rs760462817	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383874	CCTCCAGCACATTGT[A/G]GAACAGAAAAATGGC	57674
rs760467618	snp	G/T	1.64743e-05	0.00287	synonymous-codon	RNF213	GRCh38.p7	17:80344953	CCTGTTTCACTGCGG[G/T]GTAATAAACCCATCC	57674
rs760468444	snp	A/G	3.29598e-05	0.00405941	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380901	GACGTGGTGACATGT[A/G]ACCGAGGGCTGCCCC	57674
rs760474593	snp	G/T	1.6489e-05	0.00287128	intron-variant, missense	RNF213	GRCh38.p7	17:80319398	CTATGAAGCACCCGC[G/T]GGGTCTCAGCTCCTC	57674
rs760504433	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294191	GCCTAAGAACAGTCA[C/T]GAATTCAGCCCTTGC	57674
rs760507715	snp	A/G	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80309134	CAGCCTTATCTGCCG[A/G]GATTGTCTGCAGAAT	57674
rs760509164	snp	C/T	8.30848e-05	0.0064448	intron-variant	RNF213	GRCh38.p7	17:80349935	CCTTCCCTGCTGCCC[C/T]CTCCCTCCCCAGCCG	57674
rs760516407	snp	C/T	1.64746e-05	0.00287002	intron-variant	RNF213	GRCh38.p7	17:80291619	CAACCGTATCCTGTT[C/T]ATTCACAGAGACTTG	57674
rs760543061	snp	A/G	1.65614e-05	0.00287757	missense	RNF213	GRCh38.p7	17:80298353	TGAACCTGTGCCAAA[A/G]ATGCATGGACACAAG	57674
rs760543080	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260084	ACAGATGGGAAAACT[A/G]AGGCACGGGGGATGG	57674
rs760544032	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80336644	GGAAATATGCTGAAA[C/T]GTTGCCAGGAGTTTT	57674
rs760544841	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80329920	TTGAGTTCTGGGAAA[-/T]TCTCTTGAATGATTT	57674
rs760546132	in-del	-/C	1.64738e-05	0.00286995	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385110	TCTAGTGAAGCAGTT[-/C]CAGAACGTCCAGCAA	57674
rs760555300	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383522	AACAAACAACACTGA[A/C]ATTAGAAGATCAAAG	57674
rs760562491	in-del	-/CAAACTAAAGAAAGTGAAATTCTT	1.64928e-05	0.00287161	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393373	CTCGTAAGTTACATG[-/CAAACTAAAGAAAGTGAAATTCTT]CCTGAAATGGCATCT	57674
rs760565212	snp	A/T	4.95774e-05	0.00497858	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287909	CTGCCAGCCCCTGTC[A/T]CCTGACTTTGCTTTC	57674
rs760568264	snp	A/G	1.76142e-05	0.00296762	splice-acceptor-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287814	CTCTCTTTCTGTTTA[A/G]AGCAAAAAGAAGAAA	57674
rs760577912	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80348121	CCTGCTGAACTGCGC[C/T]ACGCCCGATGCCGTG	57674
rs760601641	snp	G/T	1.65386e-05	0.00287559	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361940	AGCTTGCATGATGGG[G/T]ACTGGATGCAGACAC	57674
rs760607484	snp	C/T	1.65419e-05	0.00287588	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364600	CGGATCCACCCTTTT[C/T]CGAAAGGAAGAACAG	57674
rs760608413	snp	A/G	0.00011607	0.00761718	missense	RNF213	GRCh38.p7	17:80334256	TCATCTGCTGGGTCC[A/G]GGAGGCTCTTGGAGG	57674
rs760614556	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320053	ATGCCATACGGTACA[C/T]CTGTCAAAAGTTCCA	57674
rs760617450	snp	C/T	1.64871e-05	0.00287111	synonymous-codon	RNF213	GRCh38.p7	17:80347575	CAAGGACCAAGAGTA[C/T]ACCCAGCTCTGCAGA	57674
rs760636682	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391988	GACCAGGCTGGTCTC[A/G]ATCTCCTGACCTCAA	57674
rs760643545	snp	A/G	0.000508906	0.0159435	intron-variant	RNF213	GRCh38.p7	17:80340405	TCCCAGGGACTGCCC[A/G]GGGCCCTTCCCCCCT	57674
rs760648524	in-del	-/TGTTCAG	1.64789e-05	0.0028704	frameshift-variant	RNF213	GRCh38.p7	17:80307130	TTCTCTGCCTTAGGA[-/TGTTCAG]GATGTTCAGAACGTT	57674
rs760655162	snp	C/G	1.65263e-05	0.00287452	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353031	TGTCACCATCAGCCA[C/G]CTGTTCGCGCCCGGA	57674
rs760656345	snp	A/G	1.6504e-05	0.00287258	stop-gained	RNF213	GRCh38.p7	17:80298443	GGCACAAGGATGCCT[A/G]GAGACAGCCTGAGGA	57674
rs760665858	snp	A/G			missense	RNF213	GRCh38.p7	17:80347022	CTGCCAAGATGAACC[A/G]GGGCATTTTTGTGTC	57674
rs760685786	snp	C/T	3.2963e-05	0.00405961	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386369	GCTCTCGTCAGCTAC[C/T]TGATTCGCCTACACA	57674
rs760699466	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395982	CCCTTTATTCATCCT[C/T]ACTCCCACTCATACC	57674
rs760707307	snp	C/G	1.65067e-05	0.00287282	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358294	GTGCTGCAGGCACAC[C/G]CTCTGGAAGCGGGTC	57674
rs760709798	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80338974	AAAAAAAAAAAAAAA[A/T]TAAAACAAATGATAC	57674
rs760716218	snp	G/T	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376359	TTTCACCTCCTGATA[G/T]CAGCCGTTTTGCAAC	57674
rs760717166	in-del	-/CTTA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362471	GAAAAATTGCTTAGC[-/CTTA]CTATTAATAGCAAAT	57674
rs760727218	snp	G/T	0.000249383	0.0111637	synonymous-codon	RNF213	GRCh38.p7	17:80348049	CATAGAGAGGCAGGG[G/T]CCCCGGGCCTTGACG	57674
rs760732823	snp	A/C/G	0.000115811	0.00760878	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386297	ACTGACTTGGATCTG[A/C/G]ACACTGAGTTTGAGA	57674
rs760755990	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357493	TCCAGATAAACATGT[A/G]CCTTCTTGTTTAGTT	57674
rs760777735	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293752	GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	57674
rs760787441	snp	A/C	0.000169343	0.00920016	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376985	GTTGGGGTCTAGATG[A/C]CCCCACACTCCTTTG	57674
rs760806384	in-del	-/GG			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368430	GGAATGTAGACGCCA[-/GG]GTGTTTTTTTTTTTT	57674
rs760817075	snp	C/T	1.65141e-05	0.00287346	synonymous-codon	RNF213	GRCh38.p7	17:80348127	GAACTGCGCTACGCC[C/T]GATGCCGTGGTCCGG	57674
rs760821174	snp	C/G	0.00114138	0.0238618	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288653	TGATGCTGTAGCTGA[C/G]CCAGCCAATGCAGTT	57674
rs760823446	snp	C/T	4.99122e-05	0.00499536	missense	RNF213	GRCh38.p7	17:80273277	CAATGGCGTCGGCCT[C/T]GGAGGGTGAAATGGA	57674
rs760834907	snp	C/G	0.00061862	0.0175763	intron-variant	RNF213	GRCh38.p7	17:80332646	TGTAAGTTATTTGCT[C/G]GGGACTGTGGGGGTT	57674
rs760838405	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389403	GAAATCAGCACAGCC[C/T]CTCACCCTGGTCTCC	57674
rs760841466	snp	C/G			intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319447	GAAGTGGGCACCCTC[C/G]TCCCTCGCCAAGGGC	57674
rs760848800	snp	A/G	0.000216157	0.0103938	synonymous-codon	RNF213	GRCh38.p7	17:80346516	GGATGAAATAACACG[A/G]GCACAGGATCTTTTT	57674
rs760849479	snp	C/G	3.29451e-05	0.00405851	missense	RNF213	GRCh38.p7	17:80291702	TAGATAAATACATTC[C/G]TTACAAGTACGTCAT	57674
rs760850075	in-del	-/CTGTCTTTAGGGAA			intron-variant	RNF213	GRCh38.p7	17:80270671	CCTTGAGCGGCCTGT[-/CTGTCTTTAGGGAA]CTGTCTTTAGGGAAG	57674
rs760850211	in-del	-/TCT	3.33517e-05	0.00408347	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369914	AGCCCTGGCTTTTTC[-/TCT]TCATCGCAGCGTTTT	57674
rs760852771	snp	A/G	1.73423e-05	0.00294463	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382931	TATACGCAGACTGCT[A/G]TGTTCTTTGTGCCTT	57674
rs760854766	snp	C/T	3.33428e-05	0.00408293	intron-variant	RNF213	GRCh38.p7	17:80344055	CTGGCGTGGGGGGCT[C/T]TTGGGTTCTTTCTGG	57674
rs760863610	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391079	AAACAAACAAAAAAA[A/G]GAATAGAAAAAGCTA	57674
rs760871318	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329787	AGTGAGCCGAAATCA[C/T]GCCACAACACTCCAG	57674
rs760884546	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298965	GCTTGGGCGACAGAG[C/T]GAGACTCTGTCTAAA	57674
rs760886086	snp	A/G	5.03723e-05	0.00501833	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390234	GGCGGGGCAGACACA[A/G]TGTTGTGCTGTCTCT	57674
rs760910680	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366275	CTTGAAGGGGAATTC[C/T]TGGATCATTTGATAA	57674
rs760921627	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369582	CCACCATTTGCTTCA[A/G]GGACAACGCTCCGCC	57674
rs760931335	snp	A/C	1.9832e-05	0.00314891	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363812	CCCAGGAGCCCTCAC[A/C]CACTGCTTCATCTGG	57674
rs760940521	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377114	GGCGTCTGCAGAAGA[C/T]GAATGGCTTGAAGGA	57674
rs760948706	snp	A/C			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351474	AAACGAGCCGCTAAG[A/C]GAAGATTTCTCATCC	57674
rs760950941	snp	C/G	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80307154	TGTTCAGAACGTTCA[C/G]AACATTTTAGAAATG	57674
rs760961141	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328929	TTTTGCACAAACTCT[C/T]TGTTTTCCACAGAAT	57674
rs760961284	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341346	CCATGCCTCTTGACC[C/T]ACCCTTCGTTTGCCA	57674
rs760963535	snp	C/T	1.84463e-05	0.00303691	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374725	CTGTATTGGAAGTCA[C/T]GTGCCCACAGCCTCC	57674
rs760976787	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324967	AGGTAATTTGCTTTT[A/G]TTATTTCAAAACAAA	57674
rs760986931	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80307571	TTTGTTTTTTTGAGA[A/T]GGAGTCTCACTCTTG	57674
rs760992896	snp	C/T	1.71217e-05	0.00292584	synonymous-codon	RNF213	GRCh38.p7	17:80347230	CAAAATGGTCTTTGC[C/T]GCAGCAAAGGCTTCA	57674
rs760999376	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385139	AAGTTGAATACAGCT[C/T]CATCAGAGGCTTCCT	57674
rs761001833	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377887	GGAGAGTGAGGCTCT[A/C]GGCCTTCCAGGAGAG	57674
rs761017063	snp	A/G/T	3.29453e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377765	TTCTCTTCACAGCTT[A/G/T]TCCCAACGGCCATCC	57674
rs761027115	snp	A/G	3.29506e-05	0.00405884	missense	RNF213	GRCh38.p7	17:80345654	ACCTGCGGCGTGGTG[A/G]TACCAATGCTGACAC	57674
rs761034987	snp	C/T	6.59022e-05	0.00573993	missense	RNF213	GRCh38.p7	17:80346262	CTCAGGGACGTGGAG[C/T]GCTGTGTGAAAGTTT	57674
rs761046039	snp	A/G	1.67186e-05	0.0028912	missense	RNF213	GRCh38.p7	17:80347147	GCGTCCTTTGCCAAA[A/G]CCTACGAAACGGTGT	57674
rs761046561	in-del	-/AC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391042	ACTCCAGCCTGGGCA[-/AC]AGAGGGAGACTTCAT	57674
rs761047642	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80339896	CGAGGTGTTGCCAGC[C/T]GCCCTGGCTGTCTAC	57674
rs761050375	snp	G/T	1.67086e-05	0.00289033	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388592	TTAATTTTAAAAAAC[G/T]TTTTTCTTTCCCAAT	57674
rs761055867	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375777	CTGCAAGACCCCCCA[A/G]AGCCAGCAGTCAGCC	57674
rs761074015	snp	A/G	1.66335e-05	0.00288383	missense	RNF213	GRCh38.p7	17:80295564	ACCATCAGGTGAAGA[A/G]ATACCTGTGGCAACA	57674
rs761083745	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80290603	AGGAGTCACCGTGTT[C/T]TTCCACGCCATCATC	57674
rs761089486	in-del	-/G	1.66829e-05	0.00288811	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373060	GCACCGGGTGTACCT[-/G]GTGCGGAAGCTCAGC	57674
rs761090898	snp	C/T	3.33072e-05	0.00408075	missense	RNF213	GRCh38.p7	17:80273337	GCCCGTGCTTGTTCC[C/T]GGGCTCAGACAGTTG	57674
rs761099563	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	RNF213	GRCh38.p7	17:80346174	TGAAAACGGGACTCG[C/T]GTGATCACAGAAGTC	57674
rs761110619	snp	A/G	8.36309e-05	0.00646595	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372627	CAGCAAGCCGGGGCC[A/G]AGAGCCTGCCAACGA	57674
rs761138963	snp	C/T			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372648	CTGCCAACGAGGCCT[C/T]GGTTGAATACCTGCA	57674
rs761145420	snp	A/C	1.65685e-05	0.00287819	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381019	CCAAACAATGGGCTC[A/C]GTTAAGAACCTGCTT	57674
rs761148384	snp	C/T	1.65012e-05	0.00287234	synonymous-codon	RNF213	GRCh38.p7	17:80313083	AGGGACCCTTGCTGC[C/T]ACGAAAAGGTGGCTC	57674
rs761165224	snp	A/G	3.31296e-05	0.00406985	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361711	GACGCACTCCAGGCC[A/G]CTCCTTGGTTTCCTC	57674
rs761180528	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80282435	ATGGAGTCTCACTCT[C/G]TCGCCCAGGCCGGAG	57674
rs761189212	snp	A/G/T	3.2973e-05	0.00406025	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367769	CGAGAGAACTCTGAC[A/G/T]TGAAGACGCACGGGC	57674
rs761209803	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371383	AGCGATGGGGAGCAG[A/G]GCAGGCAGGCCGCTG	57674
rs761216585	in-del	-/T/TC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356936	GGTTTTTTTTTTTTC[-/T/TC]GAGACAGAGTCTCAC	57674
rs761220586	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80323803	GTTTAAATTTTGCAC[G/T]TCTTTTGTTAAATTT	57674
rs761228213	snp	A/G/T	4.94852e-05	0.00497399	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385216	TGTCCCGCATTTGGC[A/G/T]GTTCGAAAGGATCAC	57674
rs761238344	snp	A/G	0.000114502	0.00756556	missense	RNF213	GRCh38.p7	17:80327860	ACAGAGGATGCCAAG[A/G]GGCTGATAGCTGTTG	57674
rs761238461	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285901	GGCTGGTGGCGAACT[C/T]CTGACCTCCAGTGAT	57674
rs761238603	snp	G/T	1.65515e-05	0.00287671	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288032	CCACGCCACTGGAGG[G/T]TGACGGCCTCTCCGC	57674
rs761249397	snp	C/T	0.000114279	0.00755821	missense	RNF213	GRCh38.p7	17:80339318	AAGCAGGGTGTGTCC[C/T]TCCAAATGGACTTTG	57674
rs761251696	in-del	-/C	1.64947e-05	0.00287177	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386334	GCCACGCCGACGGGG[-/C]CCTGGGCCTCTGTGC	57674
rs761257232	snp	A/C	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80290528	ACATGGCAGGTGGAC[A/C]GATCTCACGGGAATC	57674
rs761260165	snp	C/T			stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369668	TTAAGAGATGCTGCC[C/T]AGAGTAGGTTGCTTT	57674
rs761268439	snp	C/T	0.000298537	0.0122139	missense	RNF213	GRCh38.p7	17:80295645	TGCCTGTGGACTGCC[C/T]AGTGAGGAGTAAACT	57674
rs761268582	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280594	GAGTAGCTGGGACTA[C/T]AGGCGTGCACCACCA	57674
rs761272619	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292314	CTCAGGTGATCTGCC[C/T]TCCTCGACCTCCCGA	57674
rs761283759	snp	A/C			intron-variant, missense	RNF213, LOC100294362	GRCh38.p7	17:80360402	GAAGGAGTGAGAGGC[A/C]CCGGCGGGACCAGAA	57674
rs761289587	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265337	TAGGCGTGAGCCACC[A/G]CGCCCAGCCTAAGGG	57674
rs761294158	snp	G/T	3.29462e-05	0.00405857	missense	RNF213	GRCh38.p7	17:80345216	TAGCGCCCTTCTCCC[G/T]CCGGAAGAGGTGGGA	57674
rs761295414	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370281	CTGAACATGGGCTCT[A/G]TTTCCTTGGAAAGGA	57674
rs761299053	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394822	GTGACCCAGACTGCA[A/G]GCAGTAACTGACTTC	57674
rs761300590	snp	A/G	3.29538e-05	0.00405904	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353684	AAGTTCTGGTTCTTG[A/G]GACCTCCCCTTGTGC	57674
rs761314427	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265491	TGGTGACTCTGTACA[C/T]GATGCTTTTGAACAT	57674
rs761315373	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80347092	CAAGGGCATCTGCTC[C/T]TCAGACATCCTCGTC	57674
rs761318347	snp	G/T	0.000114804	0.00757554	missense	RNF213	GRCh38.p7	17:80339584	CAACTGCACCCTGAG[G/T]GATGTCTTAAGGGCC	57674
rs761341349	snp	A/G	1.6495e-05	0.0028718	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367758	TTCAGTGTCTTCGAG[A/G]GAACTCTGACGTGAA	57674
rs761345533	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80344459	CAGGAAGTTGGGTTA[C/G]AAAGTGATTTCCTGG	57674
rs761358589	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80291655	TGACCGCGTTCTTGT[C/T]GAAGGCATTGTCTGC	57674
rs761358636	snp	A/G	1.65897e-05	0.00288003	missense	RNF213	GRCh38.p7	17:80295002	AGTACAGGGAGAAAG[A/G]GGTATCAGGCTTGCC	57674
rs761366309	snp	A/G	4.94548e-05	0.00497242	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380856	GACAGAACGCAGACC[A/G]GCCACGTGCTGGGCA	57674
rs761373988	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80279170	CCCACATCCTTCCAC[-/T]TGCCTTTTTACTCCG	57674
rs761377471	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80275358	TGGGAAAGTGGCAGT[A/T]CGGATGGTGTTCCTT	57674
rs761381161	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80264112	AAAACAAGAAGTTTT[A/G]TCGGGGTCTTTGCTG	57674
rs761396078	snp	A/G	1.962e-05	0.00313203	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386873	CTTCCTCCAGGGCAA[A/G]CCCCGGCTGAGCCTC	57674
rs761415776	snp	C/G	0.000166257	0.00911596	intron-variant	RNF213	GRCh38.p7	17:80349948	CCTCTCCCTCCCCAG[C/G]CGCAGCCGTGTGGCT	57674
rs761420365	snp	C/T	1.68966e-05	0.00290655	synonymous-codon	RNF213	GRCh38.p7	17:80346990	CTTCGTGGGCATCTC[C/T]AACTGGGCCCTTGAC	57674
rs761422022	snp	G/T	1.64749e-05	0.00287005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383887	GTGGAACAGAAAAAT[G/T]GCAAAGAAAGAGTGC	57674
rs761424989	in-del	-/AAC			intron-variant	RNF213	GRCh38.p7	17:80343658	GTATTTATGTGTCTA[-/AAC]ATAAAAATGGTACAG	57674
rs761452107	snp	C/T	1.66849e-05	0.00288828	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373053	ACGACTGGCACCGGG[C/T]GTACCTGGTGCGGAA	57674
rs761472839	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380724	CAGCAAGTACTCTTC[A/G]CATAACTCTCTTCTC	57674
rs761474968	snp	A/T	1.66468e-05	0.00288498	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372011	TCTCTCTTCCCTGAA[A/T]TTCTTTTGGAAACTA	57674
rs761476891	in-del	-/CACGTGTGTGTGCG			intron-variant	RNF213	GRCh38.p7	17:80290322	GTGTGCGTGTGCGTT[-/CACGTGTGTGTGCG]CACGTGTGTGCGTGT	57674
rs761479483	snp	A/G	1.98304e-05	0.00314878	missense	RNF213	GRCh38.p7	17:80289804	AGAAGGAGCAAAAAA[A/G]CCAGGAAGCAGATGT	57674
rs761480690	snp	A/T	1.66449e-05	0.00288482	missense	RNF213	GRCh38.p7	17:80346525	AACACGGGCACAGGA[A/T]CTTTTTCTGGACGGC	57674
rs761490483	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259511	ACCCTAAAATTAAAA[A/G]TTTATCCTCAGGTTT	57674
rs761494803	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280688	TCAAACTCCTGGGCT[C/T]AAGCAATTCTCCCGC	57674
rs761514803	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80301664	AGTGAGGATGTGGGA[A/T]AGAGAAACTCTCATA	57674
rs761521948	snp	C/T	3.29881e-05	0.00406115	intron-variant	RNF213	GRCh38.p7	17:80309215	CACCCGGGATAGGTG[C/T]GGAATTTCAAGCAGC	57674
rs761528748	snp	G/T			missense	RNF213	GRCh38.p7	17:80327987	TTGACATCTGGCAAC[G/T]GAGTAAGCATCGAGT	57674
rs761541104	snp	C/T	1.67702e-05	0.00289566	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354023	TCCACCAACAGGTGT[C/T]GATCCTGGACACCAC	57674
rs761546134	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80345181	CATGGTCACCATGGA[C/T]GGGGTTAGGGAAGAA	57674
rs761558360	snp	A/G	3.58494e-05	0.0042336	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288019	CCAGGCACAGCCACC[A/G]CGCCACTGGAGGGTG	57674
rs761566335	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285042	AGCCAAGGGACCATT[C/T]CCCAGGATGGGCCAT	57674
rs761572217	snp	A/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80345109	CTTCATGATCTTTAT[A/G]GCAAGAGATTTTGCC	57674
rs761572358	snp	G/T	1.64838e-05	0.00287083	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363231	CGTCTGCAGAACTTT[G/T]CCAGAATCCTGACCA	57674
rs761593738	snp	A/G	1.64803e-05	0.00287052	missense	RNF213	GRCh38.p7	17:80347705	TACTACGTCCACCTC[A/G]GCGGCCAGAAGTACG	57674
rs761602507	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317573	ATGCTGTGTTTACTT[A/G]GCCCGCCGTGCTCAA	57674
rs761603021	snp	C/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80345605	ATGGGAGAAACTGGC[C/T]GTGGGAAAACCAGGC	57674
rs761603859	snp	C/G	1.64814e-05	0.00287061	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380917	ACCGAGGGCTGCCCC[C/G]AGTGGTCTTCCTCCT	57674
rs761606665	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376413	CATTGTTGAGGGCGG[A/G]GCCTAGTGACAGCAA	57674
rs761615703	snp	A/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80309142	TCTGCCGAGATTGTC[A/T]GCAGAATGATTAGAC	57674
rs761616396	snp	G/T	1.65061e-05	0.00287277	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389783	ACGACATGAGTGGGG[G/T]TGTGAGACCTCAGCC	57674
rs761618243	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80327187	TTTTTAAAGAAGATT[C/G]TGTGTATTCTATTTA	57674
rs761648722	snp	C/T	1.65051e-05	0.00287267	missense	RNF213	GRCh38.p7	17:80298451	GATGCCTGGAGACAG[C/T]CTGAGGACACCTGGG	57674
rs761653011	snp	A/G	1.64844e-05	0.00287087	missense	RNF213	GRCh38.p7	17:80347594	CAGCTCTGCAGAAAC[A/G]TCAATCGTGTGAAGA	57674
rs761654376	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80295247	CCCTGGCCTTGGAGG[G/T]AGAGTGGAAGGAACG	57674
rs761656088	snp	A/G	1.73396e-05	0.0029444	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288401	CCTGGGAGTGGCACT[A/G]AGCCCTCGGCACCTG	57674
rs761666712	in-del	-/CTC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384299	GCAGATCAAACAAAA[-/CTC]CTCCCTGTGCCTAAG	57674
rs761694802	snp	A/G	1.73486e-05	0.00294517	intron-variant	RNF213	GRCh38.p7	17:80343088	GCTAGGATTACAGGT[A/G]TGAGCCACCACTCCC	57674
rs761695851	in-del	-/CAT	1.64874e-05	0.00287113	intron-variant	RNF213	GRCh38.p7	17:80307235	GCAGTCTCTCCCTCA[-/CAT]GCGGCCCCCGGGGGC	57674
rs761704553	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80337346	TGTGCCAGCCGGGGC[A/T]CCAGGCACTGGAGGA	57674
rs761705373	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374329	CCTGCCTCAGGCCAG[C/G]TCAGGGAATCCCAGC	57674
rs761710252	snp	C/G	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369591	GCTTCAAGGACAACG[C/G]TCCGCCTGAGAAGGA	57674
rs761712640	snp	C/T	0.000143668	0.00847427	intron-variant	RNF213	GRCh38.p7	17:80336493	AGGTTTGTACACAGC[C/T]GTTTTCAATGATATT	57674
rs761713794	in-del	-/T	8.23662e-05	0.00641688	frameshift-variant	RNF213	GRCh38.p7	17:80343952	TCGGAACCCCTGCCA[-/T]TTGTATATCGTTGAA	57674
rs761715604	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292150	AGTACAGTGGTGCGA[C/T]CTCGGCTCACTGCAA	57674
rs761760235	snp	C/T	1.66788e-05	0.00288775	missense	RNF213	GRCh38.p7	17:80346617	TCGTCTGCATCGAGC[C/T]GAAGATTCCCCTCTT	57674
rs761760577	snp	A/C	3.2956e-05	0.00405918	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379615	GTGCCCTGTCTTCAC[A/C]CTAGTGTGGCAGGCC	57674
rs761761703	snp	A/G	1.64808e-05	0.00287057	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369525	TTGAAAAGCATGCCC[A/G]CTTCCGGCAGATGTG	57674
rs761764136	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355522	GGGAATGGGGGCTTA[-/C]AGGGGGAAGAAGCGG	57674
rs761766679	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279581	GCGATTCTCCTGCCT[C/T]ACCCTCCTGAGTAGC	57674
rs761787979	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384927	CACAGGAAATGACAC[C/T]GACCAGATTAAGCTA	57674
rs761789068	snp	C/T	0.000181604	0.00952727	synonymous-codon	RNF213	GRCh38.p7	17:80348202	GCAGGAGTACTTTCA[C/T]AGACAGAGGCACAAC	57674
rs761802191	snp	A/G	0.000114712	0.0075725	missense	RNF213	GRCh38.p7	17:80336167	CTTCCCCAGGCATCA[A/G]TGAGCTGAAGGTGTT	57674
rs761835688	snp	A/C	1.68018e-05	0.00289838	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373105	GGAGTTCGTGCAGGG[A/C]CTCTCCAAGCCCGGC	57674
rs761842740	snp	C/T	1.68621e-05	0.00290358	intron-variant	RNF213	GRCh38.p7	17:80298541	GTAGAGTTGTGCTTA[C/T]CTACATGAATCTGGG	57674
rs761852768	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80313594	AGGTGGTGGAGGTGA[-/TGG]TGGTGGTGGAGGTGA	57674
rs761867551	in-del	-/CC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378211	CATGGGGTCAGTGAG[-/CC]CCTTGTCTTGATAGA	57674
rs761868221	snp	G/T	1.69856e-05	0.00291419	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383079	ACTGGAGGTAAGCAG[G/T]AAGTGCTGACAGCTG	57674
rs761878278	in-del	-/AT	1.65875e-05	0.00287984	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371934	AAAAAGAAAGCATTC[-/AT]ATAACTGAAGATAAA	57674
rs761896281	in-del	-/ACACCCCAAACCCAC	2.53534e-05	0.00356034	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373216	CCCCCACAGCCCCAT[-/ACACCCCAAACCCAC]ACACCCCCCTACCCT	57674
rs761899304	snp	A/G	1.71135e-05	0.00292514	missense	RNF213	GRCh38.p7	17:80347246	GCAGCAAAGGCTTCA[A/G]ATAGAAAGCCTTCCC	57674
rs761911208	snp	A/G	0.000115313	0.0075923	synonymous-codon	RNF213	GRCh38.p7	17:80307172	CATTTTAGAAATGCT[A/G]TTGCGACTCCTGGAC	57674
rs761923278	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80268088	TGCCTCCCAAAGTAC[C/T]GGGGCTATAGGCATG	57674
rs761933519	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80274423	GCGGCCTGGGAAGAC[C/G]CAGAGGGCAGTGTCA	57674
rs761944656	snp	C/T	1.64914e-05	0.00287149	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361740	TCTCTGCAGGACTGC[C/T]CAAGAAGTTCGTGGA	57674
rs761953875	snp	A/C	1.70705e-05	0.00292147	intron-variant	RNF213	GRCh38.p7	17:80273442	CCTCCGCCCCCGCTC[A/C]CTCTGCCCAGGAAAA	57674
rs761954494	snp	G/T	1.65037e-05	0.00287256	intron-variant	RNF213	GRCh38.p7	17:80307241	TCTCCCTCACATGCG[G/T]CCCCCGGGGGCTTCC	57674
rs761959065	snp	C/G/T	3.29578e-05	0.00405931	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393428	AGTTCCCAGAAGAGA[C/G/T]ACTGCTCGCCAGCTG	57674
rs761967366	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80344751	CTCCCAAAGAGGTGA[C/T]AGACATGGAGCTGAG	57674
rs761967798	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393153	GCCCAGCTAATTTTT[A/G]TATTTTTGCTAGAGA	57674
rs762003841	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80330029	TCTCTCGGATTTTCT[A/G]TCTCTGTTTTTTGCT	57674
rs762005057	snp	A/T	3.29484e-05	0.00405871	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288699	GAAATGAAAGAGAAG[A/T]CCCAGAGAATGAAAC	57674
rs762013253	snp	A/G			intron-variant, missense	RNF213	GRCh38.p7	17:80278813	TAGACCTCATATCCG[A/G]TGAATGGGAAGCTGC	57674
rs762020411	snp	C/G	1.67377e-05	0.00289284	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393295	GCTTACACACGTGAG[C/G]CACCATGCTGAGGAG	57674
rs762035520	in-del	-/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361165	ATCTAGATGTTTCTC[-/T]TTGGGGCTAGCTTGG	57674
rs762053807	snp	A/G	1.64836e-05	0.0028708	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364439	TTTTGACAGAGCCCA[A/G]TGGAGTCGGATTTTC	57674
rs762055802	snp	A/G	6.66245e-05	0.00577129	missense	RNF213	GRCh38.p7	17:80273348	TTCCCGGGCTCAGAC[A/G]GTTGGCAAGAAAACC	57674
rs762056089	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392063	GTGAGCCACTGCGCC[C/T]GGCCTGTCCTCTCTC	57674
rs762072784	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331240	GACATAAAACTACTC[A/G]GCTCTCAGTGTTGCC	57674
rs762095614	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341457	AACATTACTCTTCCC[C/T]TCCCTGCTGAAGCCT	57674
rs762121601	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80300236	CCTTTTAATAGCAGC[C/T]ATTCTGACTGGTGTT	57674
rs762123558	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80262559	CCCTCTAGGCAGATA[A/G]TGGGGCCTCAGAGAG	57674
rs762159286	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387902	GTCATATCTACTGTA[C/G]TTATGTACGGTACCA	57674
rs762159935	snp	C/G	1.65002e-05	0.00287225	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388731	CACGGGGCTTTCTGC[C/G]TTCTCAGTGTGTTTC	57674
rs762168046	snp	G/T	0.00011411	0.0075526	missense	RNF213	GRCh38.p7	17:80328427	AGAAAGAGAAAAGAT[G/T]TGTTGATAGTCTCCT	57674
rs762168202	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372893	CCTGTGGGTAGGTCC[G/T]ATGCCCTCTGGTTGG	57674
rs762169854	snp	C/G/T	3.2948e-05	0.00405871	missense, synonymous-codon	RNF213	GRCh38.p7	17:80344873	AATCAAAACCAAGAC[C/G/T]TAGACACGTTTCAGT	57674
rs762175075	snp	A/G	1.6476e-05	0.00287014	missense	RNF213	GRCh38.p7	17:80346268	GACGTGGAGCGCTGT[A/G]TGAAAGTTTTCAGGT	57674
rs762182653	snp	A/G	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367897	AATTCTGAACCTCTC[A/G]TGGTTTTCACTTCTT	57674
rs762189117	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268436	ACCACCAAGCACTCC[A/G]AAGATGCAGGGGTGG	57674
rs762205773	in-del	-/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367277	CTGGGGAGGGACGGA[-/G]GGGATGTGAAGTTGT	57674
rs762209364	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80313125	TACAAAGAACATGCT[C/T]ACATCTTCAGGTGCC	57674
rs762210944	snp	A/T	1.68431e-05	0.00290194	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372707	GACAGAGCTGCAGAT[A/T]TCCTCTCGGAGCCTG	57674
rs762214390	snp	A/G	2.00351e-05	0.00316498	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373196	GGGCAGCACACAAAC[A/G]TGCACCCCCACAGCC	57674
rs762233550	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80345298	ATTCATCGGCTTCCA[C/T]CTGCAGCCCAACATC	57674
rs762250155	snp	A/G	3.30011e-05	0.00406195	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385221	CGCATTTGGCGGTTC[A/G]AAAGGATCACTGCAT	57674
rs762250229	snp	C/T	1.66863e-05	0.0028884	missense	RNF213	GRCh38.p7	17:80347319	AGGATGACATCCAAG[C/T]TTTGGACATCTTTCT	57674
rs762251572	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366405	CCACATCATGGGCAA[C/T]ACCTGTTACTATCTG	57674
rs762253618	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379206	TCATAAAAATTGATA[G/T]ATGAAAAAGTCCAAA	57674
rs762254832	in-del	-/TATT			intron-variant	RNF213	GRCh38.p7	17:80325941	TGTGTTATTTGTATT[-/TATT]TATTTATTTATTTAT	57674
rs762259446	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368010	GATGCAAAGGACCCC[A/G]TCTGTCTGCCCTGCG	57674
rs762275165	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80306281	AGTTTATGAGAGAGA[A/G]GCAGCATTTGCTGAG	57674
rs762284839	snp	G/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80295772	CAGCTCACCAGATGA[G/T]TTTCACCGTGACCTA	57674
rs762294697	snp	C/T	1.66918e-05	0.00288888	synonymous-codon	RNF213	GRCh38.p7	17:80340148	AGACTACCAGCTCGT[C/T]ATGGTCTGTGATGGG	57674
rs762297341	snp	G/T	1.89295e-05	0.00307643	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376860	ACTTATCTAGAGCTG[G/T]CTCTGTCTTCTTGTT	57674
rs762307340	snp	A/G	1.65053e-05	0.0028727	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354400	CGGAGCCAACAGCTC[A/G]GCCACGGCCATGCTG	57674
rs762310684	snp	C/G	3.29457e-05	0.00405854	missense	RNF213	GRCh38.p7	17:80290607	GTCACCGTGTTCTTC[C/G]ACGCCATCATCTCTC	57674
rs762326641	in-del	-/TATT			intron-variant	RNF213	GRCh38.p7	17:80305038	TGAATTCTTTTTGTG[-/TATT]TATTTATTTATTTAT	57674
rs762326745	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393268	TTACACACGTGAGCC[A/C]CACAGTGCTGGGCTT	57674
rs762326844	snp	C/G	1.66186e-05	0.00288254	intron-variant	RNF213	GRCh38.p7	17:80312963	CATCTCGCCGGGAAC[C/G]TGAGTCCACAGCCGA	57674
rs762335250	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80271701	GAAAAAGAAAAGGCC[A/G]GGTGTGGTGGCTCAA	57674
rs762343505	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378081	GTCCCTGGATGCCAG[A/G]AGCACCCACTCCTCC	57674
rs762347582	snp	C/T	3.40408e-05	0.00412544	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288171	AGGGGAGGACCAGGA[C/T]GCTTCCATCCCCTCT	57674
rs762348670	snp	G/T	1.66355e-05	0.002884	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376544	CCAGCCACCATGGCG[G/T]TAAGAGTAGGCCACA	57674
rs762352577	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362179	TAAATGTTGAGTTTC[C/T]CTTGAAAAAAATTAA	57674
rs762352884	snp	C/G	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345363	GGAAGGTCATCAAGA[C/G]AGACGTCATGACCAG	57674
rs762361524	in-del	-/AG			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398794	GAAAAAAAGAAAAAA[-/AG]AGATATATATACAAG	57674
rs762369786	snp	G/T	1.64841e-05	0.00287085	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380926	TGCCCCCAGTGGTCT[G/T]CCTCCTTATCCGGCT	57674
rs762374206	snp	A/G	3.29745e-05	0.00406031	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351744	ACCGTATCTTCGTCT[A/G]TTTCATCACAAAACT	57674
rs762385225	snp	C/T	0.00016159	0.00898715	intron-variant	RNF213	GRCh38.p7	17:80327792	GGGAGCCCACTGTGT[C/T]AACTGTGTTCTTCAT	57674
rs762389238	in-del	-/TATC			intron-variant	RNF213	GRCh38.p7	17:80269707	TGTATCTATCTTATG[-/TATC]TATCCATTCATCTAT	57674
rs762403311	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387156	AACAGGGTCTCACTC[C/T]GTCACCGAGGCTGCA	57674
rs762408585	snp	C/T	3.295e-05	0.00405881	intron-variant	RNF213	GRCh38.p7	17:80290519	TGTGCATGCACATGG[C/T]AGGTGGACAGATCTC	57674
rs762424017	in-del	-/TT	2.62488e-05	0.00362267	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351640	TTGTTTTTGTGTGTG[-/TT]TGTTTGTTTTTAAAA	57674
rs762428250	snp	A/G	3.29728e-05	0.00406021	missense	RNF213	GRCh38.p7	17:80347601	GCAGAAACATCAATC[A/G]TGTGAAGATCTGCAT	57674
rs762431090	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394951	GGGTGTGGGGGCCGG[A/G]GGCTGGCTTGCTGAA	57674
rs762433367	snp	C/T	6.55616e-05	0.00572508	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288072	GGTTGGCGACAGCCC[C/T]CTGCAGGCCCAGGCT	57674
rs762435600	snp	C/G	1.6477e-05	0.00287024	missense	RNF213	GRCh38.p7	17:80290685	GGAGAAGAATTTGGG[C/G]AGTCAAAATGGGACA	57674
rs762443149	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80266222	CGAGGTGAGTAGATC[A/G]CTTGAGCCCAGGAGT	57674
rs762473287	snp	A/G	3.65344e-05	0.00427386	missense	RNF213	GRCh38.p7	17:80339945	CCCCTGCCCACTTAC[A/G]ATGAGGTGCTGCTCT	57674
rs762494247	snp	A/C	3.37587e-05	0.00410831	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363346	CCTGCCCTGAGCAAG[A/C]CTTGTGGTGCTTCCA	57674
rs762501640	snp	C/G/T	0.000115481	0.00759792	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389797	GGTGTGAGACCTCAG[C/G/T]CCCCACTCAGGAATT	57674
rs762509718	snp	A/G	1.65751e-05	0.00287876	missense	RNF213	GRCh38.p7	17:80350359	CAGACAGATTTTGAA[A/G]ATGGAATCCGTAGCG	57674
rs762524713	snp	C/T	1.648e-05	0.0028705	stop-gained	RNF213	GRCh38.p7	17:80347711	GTCCACCTCGGCGGC[C/T]AGAAGTACGTGGACC	57674
rs762539790	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80345202	TAGGGAAGAAGATCT[A/G]GCGCCCTTCTCCCTC	57674
rs762540514	snp	A/G	3.29462e-05	0.00405857	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385117	AAGCAGTTCCAGAAC[A/G]TCCAGCAAGTTGAAT	57674
rs762564196	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80281763	CGGTTCCAGGACCGC[A/G]GAGGACGCCAAAATC	57674
rs762574163	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334772	GCTGGGACTACAGGC[A/G]ACCGCCACCACGCCC	57674
rs762586000	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369595	CAAGGACAACGCTCC[A/G]CCTGAGAAGGAAGTG	57674
rs762610174	snp	C/T	9.88354e-05	0.00702908	intron-variant	RNF213	GRCh38.p7	17:80306247	TCCCTATTTCTCTTA[C/T]GCAGGAGTTCCCTAC	57674
rs762615547	snp	C/T	3.51908e-05	0.00419454	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288023	GCACAGCCACCACGC[C/T]ACTGGAGGGTGACGG	57674
rs762621760	snp	G/T	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367858	CAGCAGGTGAGACCT[G/T]AGGTTTGGATCTGTG	57674
rs762638945	in-del	-/TTCCCTGCC	0.000561195	0.0167416	intron-variant	RNF213	GRCh38.p7	17:80349912	AGAAGTCCGGTGAGG[-/TTCCCTGCC]TTCCCTGCCTTCCCT	57674
rs762640250	snp	C/T	1.68895e-05	0.00290593	intron-variant	RNF213	GRCh38.p7	17:80298547	TTGTGCTTATCTACA[C/T]GAATCTGGGAAGACT	57674
rs762648576	snp	C/T	1.64814e-05	0.00287061	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358324	CCAAGGTGCTGTCAC[C/T]CCTCTGCTGGCGAGC	57674
rs762659863	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80333819	AAGCAACAGTAGTTA[C/T]TTGGCAGGGTTATGT	57674
rs762666499	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355634	GGGAATGGGGGCTTA[C/T]AGGGGAAGAAGCGGG	57674
rs762673776	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80294055	TGATTTTTACTTCTG[-/T]TTGTAGGTCTTCACG	57674
rs762678361	snp	C/T	1.68335e-05	0.00290111	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373111	CGTGCAGGGCCTCTC[C/T]AAGCCCGGCCGCCCG	57674
rs762681030	snp	C/G	1.64955e-05	0.00287184	intron-variant	RNF213	GRCh38.p7	17:80319148	GAGCACTGGAGCGCT[C/G]CATCCGAAAGCTCTG	57674
rs762692871	snp	C/T	1.67719e-05	0.0028958	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383656	ACTTCCAGAATTTTT[C/T]TTTTCATTTTCTCCA	57674
rs762703892	in-del	-/AG	1.64784e-05	0.00287035	frameshift-variant	RNF213	GRCh38.p7	17:80344841	TCCAAAGACCTTACC[-/AG]TATTTAAGACGATTC	57674
rs762713585	in-del	-/AAA			intron-variant	RNF213	GRCh38.p7	17:80315217	GGAGGTGATGGTGGT[-/AAA]GGTGGTGGTGGAGGT	57674
rs762713657	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80277337	CCCGGTGGCTTCTCA[-/C]CTGTAATCCCAGCAC	57674
rs762731239	snp	A/G	3.29462e-05	0.00405857	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376441	CAACCTTGATGGAAC[A/G]GTGACAGAAATGGCC	57674
rs762734012	snp	C/T	1.66935e-05	0.00288903	synonymous-codon	RNF213	GRCh38.p7	17:80346744	CCTGAAGCAGGTCCA[C/T]CTGGTGTCCTTCCAG	57674
rs762749876	snp	C/T	1.64762e-05	0.00287016	missense	RNF213	GRCh38.p7	17:80345702	TGCACGGAGGAACAA[C/T]TGCAGACATGATCTA	57674
rs762754977	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80303515	CTTGCCTTTAGAAGG[C/T]GTAAAAGCCTTTGGA	57674
rs762757986	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80283206	ACTGGCAGCACAGGG[C/G]GCCTACCAGGGCACT	57674
rs762758341	snp	A/G	1.64885e-05	0.00287123	missense	RNF213	GRCh38.p7	17:80347801	ATTGAAGAGAAAGAC[A/G]TCGTGTACAAACACT	57674
rs762763547	snp	C/G			missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354499	AAAGAAGCAAGAAGA[C/G]AGCCAGTTTCACCCT	57674
rs762764474	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318476	TGACAGGAACCTCAT[A/G]ACACACAAGTGGAGA	57674
rs762777382	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80275538	CACAAATGCTCGAGC[A/T]GGACGCACTCGAAAA	57674
rs762792724	snp	A/C/T	3.31561e-05	0.0040715	synonymous-codon	RNF213	GRCh38.p7	17:80291826	ACTTCTGGGCTCAGG[A/C/T]GGTAAGTCGTGGCAG	57674
rs762803483	snp	A/G	3.30896e-05	0.00406739	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381660	ACACAGTGCCGACGA[A/G]ACCATCGGCGTGGTC	57674
rs762806281	snp	G/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80258904	GTACCTGCTGCAGCA[G/T]CTGGTAGGGGCAGAC	57674
rs762810233	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390777	TGATAGAAAAAGCTA[C/T]CCTAGGCCGGGTGTG	57674
rs762818139	in-del	-/AC			intron-variant	RNF213	GRCh38.p7	17:80264725	ACAGTCAAACCACAG[-/AC]CCCCTTACAAGATCC	57674
rs762824432	snp	A/T	1.66369e-05	0.00288412	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393319	TGAGGAGACTGTTTT[A/T]AATGCTCTCTTCTTT	57674
rs762852403	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328010	CATCGAGTCGATACG[C/T]ACTTCAGGCTCCTGA	57674
rs762858000	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80281538	ACATGCCCCACTCAT[A/C]CCACTCACACACCCC	57674
rs762864847	snp	G/T	1.99285e-05	0.00315655	intron-variant	RNF213	GRCh38.p7	17:80343331	GACCTCCTCAGTAAG[G/T]GCCCTCCAGCGTCAG	57674
rs762884672	snp	C/G	1.64741e-05	0.00286998	synonymous-codon	RNF213	GRCh38.p7	17:80344941	CCTCCAGCATTTCCT[C/G]TTTCACTGCGGGGTA	57674
rs762895297	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286804	CTGACCTGATCCACA[C/T]GCACCCCTGAGTACT	57674
rs762897909	snp	C/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259387	GCATGAGAATCACTT[C/G]AACTGGGAGGTGGAG	57674
rs762898923	snp	C/G	1.65012e-05	0.00287234	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375875	CCACGCCAGAGGTGA[C/G]TAACCGCCTGCAGGG	57674
rs762913878	snp	A/G	3.29587e-05	0.00405934	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393436	GAAGAGATACTGCTC[A/G]CCAGCTGTGTCTCAG	57674
rs762914898	snp	C/T	1.64841e-05	0.00287085	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364446	AGAGCCCAGTGGAGT[C/T]GGATTTTCTCCACCG	57674
rs762914941	snp	A/T	3.29614e-05	0.00405951	intron-variant, stop-gained	RNF213	GRCh38.p7	17:80319388	CAGCTAAGGGCTATG[A/T]AGCACCCGCTGGGTC	57674
rs762922298	snp	C/T	3.29554e-05	0.00405914	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379630	CCTAGTGTGGCAGGC[C/T]GATGGAACAGAGCAT	57674
rs762924359	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383748	CAGCTCTAACCCTGT[A/G]GCCAAAATAATATAT	57674
rs762924746	in-del	-/ATCACGTGACACTGTATTGGAA	8.76616e-05	0.0066199	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374699	CCACTGATGCAGCCC[-/ATCACGTGACACTGTATTGGAA]GTCACGTGCCCACAG	57674
rs762926327	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389934	TAAGTCTGGTCTCTT[A/C]CTCTCTGCTGGACAG	57674
rs762926741	snp	A/G	1.67097e-05	0.00289043	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376928	TGCTGGCTCAAGCTC[A/G]GAGGTGGAAGGGTCT	57674
rs762937384	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375801	GTCAGCCTACTTCCT[A/G]TTAACACTGTTTAGA	57674
rs762944488	snp	C/T	4.95119e-05	0.00497529	missense	RNF213	GRCh38.p7	17:80348225	GGCACAACTCCTTTG[C/T]AGATTTCCTTCAGGC	57674
rs762954336	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80350010	TGAGCGCCACAGTCA[C/T]GTGACTGTGAAATAG	57674
rs762969923	snp	A/C/G	3.29594e-05	0.00405941	synonymous-codon, missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369670	AAGAGATGCTGCCCA[A/C/G]AGTAGGTTGCTTTCT	57674
rs762974907	snp	C/T	1.64972e-05	0.00287199	intron-variant, utr-variant-5-prime	RNF213	GRCh38.p7	17:80288807	CTCTCCTGCCCACGG[C/T]TGCGCCTCTTTCATT	57674
rs762994093	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269661	ATTCATCCATCAATC[C/T]ATCCATCCATCCATT	57674
rs762996764	snp	C/T	1.64803e-05	0.00287052	missense	RNF213	GRCh38.p7	17:80345767	GCCAATAAGGACCAA[C/T]ATCAGTTGGACACCA	57674
rs763014596	in-del	-/CCATCGGCCTGC	1.64787e-05	0.00287038	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379611	CTAGTGCCCTGTCTT[-/CCATCGGCCTGC]CACCCTAGTGTGGCA	57674
rs763029820	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383408	CCATTAAAAATGAAC[C/T]GACAATCATAGATTA	57674
rs763037354	snp	A/G	1.65479e-05	0.0028764	missense	RNF213	GRCh38.p7	17:80295677	AAAACAGGCCTGATT[A/G]TCCTTTTTGTAGTGG	57674
rs763045461	snp	A/G			intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321569	CATGTTTAATTGTTT[A/G]AAGAACTGTCCGGCC	57674
rs763070975	snp	A/C	1.65954e-05	0.00288053	missense	RNF213	GRCh38.p7	17:80340166	GGTCTGTGATGGGGA[A/C]TGGGAGCACTGCTAC	57674
rs763079495	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395602	AAGGAGTCCCCCATG[C/T]CCTGCCTGAAATGAC	57674
rs763083933	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80280485	TTGAGGCAGGGTCTC[G/T]CCCTGGGTCCCAGGC	57674
rs763090525	snp	A/G/T			intron-variant	RNF213	GRCh38.p7	17:80311288	TAGGTGTCTGCTGCT[A/G/T]TGAAGGCTCCAGGGT	57674
rs763117045	snp	A/G	6.59783e-05	0.00574324	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354549	AAGCCTGCAACCAGG[A/G]CGCTCTCCAGGAGGC	57674
rs763128869	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	RNF213	GRCh38.p7	17:80344881	CCAAGACCTAGACAC[A/G]TTTCAGTATCAAGAA	57674
rs763130760	snp	C/T	1.68989e-05	0.00290674	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372714	CTGCAGATTTCCTCT[C/T]GGAGCCTGAGGGAGG	57674
rs763140836	snp	C/T	1.6476e-05	0.00287014	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381548	CGTTGCCCCCACAGG[C/T]TCTGATAAACATCAT	57674
rs763157286	snp	C/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320870	GGCACACCTGTGGTC[C/G]CAGCTACTTGGGAGG	57674
rs763170280	snp	C/G	1.64985e-05	0.0028721	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361907	GATGTTTAGATACTG[C/G]CTAAGGGTCAGGTGT	57674
rs763173645	snp	C/T	2.20977e-05	0.00332391	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381761	GCTGGGCGGGGATCA[C/T]ACAGCACAACGGCAG	57674
rs763184514	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384346	TGGAAGACGGGAGTG[A/G]GTGGGTGTGTGCCGG	57674
rs763192482	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80349520	CAGAGACACGGGCCT[C/T]TGGGGAGGAGAGGAA	57674
rs763195727	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270291	CCTTGTCCTGCTGTT[C/T]TGCCGTGACATAGGC	57674
rs763196124	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393178	TAGAGACAGGGTTTC[A/G]CCATGTTGCCCAGGC	57674
rs763202278	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390082	CTAAGCTCCTCAGCA[C/T]ATTCCTAAATCAGAC	57674
rs763209459	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375599	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGTTAGA	57674
rs763210382	in-del	-/GTGTGTGC			intron-variant	RNF213	GRCh38.p7	17:80290407	TGTACGTGTGCTTGT[-/GTGTGTGC]GTGTGTGCGAGTGTG	57674
rs763215895	snp	C/T	6.60535e-05	0.00574651	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352891	CTTAGGGCTGAGCAG[C/T]AGCCGGGAAAGACAC	57674
rs763220829	snp	C/T	4.97698e-05	0.00498823	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360118	GAACCTTTCCGAGAA[C/T]GCTTCCAACAACGTC	57674
rs763231621	snp	C/G	4.9645e-05	0.00498197	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372944	GCCCTAAGTCACCAG[C/G]CACTCACCCGCTTTC	57674
rs763238902	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80332103	CACCTCCTCGAACTC[A/G]CAGAGGGCAACGCAT	57674
rs763243455	snp	A/G	0.000235322	0.0108446	missense	RNF213	GRCh38.p7	17:80332201	TCCAGCTCTTCTGGC[A/G]GGAAGCCGCAGAGCC	57674
rs763246693	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80331308	GTGTCATTTACCACT[G/T]GTTCAGCTCGTTTTC	57674
rs763265669	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376884	TCTTGTTTTTCAGCA[C/T]GCTTTTCTTCCAACC	57674
rs763266687	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393796	AACATTGTTTACATT[C/T]CAGGAGACTTGTAGC	57674
rs763287896	in-del	-/AGA			intron-variant, cds-indel	RNF213, LOC100294362	GRCh38.p7	17:80360725	CTGCTGCCAGATGCC[-/AGA]AGATTTGCCCTAGTC	57674
rs763289074	snp	A/G	5.05378e-05	0.00502656	missense, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385621	TCGCTTGAGACGAAC[A/G]GTTAGTATCCTGTCC	57674
rs763302578	snp	C/T	3.3083e-05	0.00406699	missense	RNF213	GRCh38.p7	17:80348015	ACTCGGACGCCTGCG[C/T]GTCTGTGGTGCTGCA	57674
rs763302781	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380516	TGTTCTTAGCCCAAC[C/T]GCTCCTCTCCTGACA	57674
rs763307556	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359186	CAATAGCTTCCACTT[C/T]AGCTTTCAGGGGCTT	57674
rs763322275	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363046	GATTTCCCACGGGGA[A/G]AACATACCATTTTTG	57674
rs763329810	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80274636	GGGGTGTCTGTGGGG[G/T]GTGTGGGGTGAGTGT	57674
rs763331601	snp	A/C	0.000145911	0.00854015	intron-variant	RNF213	GRCh38.p7	17:80331980	TTAGAGCTTTGACTT[A/C]TGACACTTTCTTTTC	57674
rs763335888	snp	A/G	5.14787e-05	0.00507314	synonymous-codon	RNF213	GRCh38.p7	17:80340292	GAAGCAGACCCTGTC[A/G]GCGGCAGCCGTGTTC	57674
rs763336849	snp	A/G	2.04489e-05	0.0031975	intron-variant	RNF213	GRCh38.p7	17:80317175	GGGTGTGACCTGTGT[A/G]CGGGTTTTGCAGGTC	57674
rs763347545	snp	C/T	6.61726e-05	0.00575169	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360055	TCATCCCTCACCTTA[C/T]TGCAGACATAAAGGT	57674
rs763350139	snp	A/G	1.65031e-05	0.00287251	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368135	TCCAGCTGTTTCCCA[A/G]GCGCACAGGTACAAC	57674
rs763352385	snp	C/T	5.02256e-05	0.00501102	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363619	CCCAGACCCTGGACG[C/T]ATTTGCCGCAATGGC	57674
rs763363712	snp	C/T	1.65225e-05	0.00287419	missense	RNF213	GRCh38.p7	17:80347963	CATTTCCAGAAGAGG[C/T]ACAAATACAGCCCCT	57674
rs763382074	snp	C/T	1.65023e-05	0.00287244	missense	RNF213	GRCh38.p7	17:80346425	GTTACCATGCCTCTT[C/T]AGAAAAGAAAGACTC	57674
rs763396377	in-del	-/CT	1.69321e-05	0.0029096	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354185	TGAGCCTCCCCACCC[-/CT]CTTGCCCCTGCCCCC	57674
rs763397098	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368903	CCTTCCCCTTCCCCC[A/C]TTCTCAGGCCTCCTA	57674
rs763412422	snp	A/G	4.9516e-05	0.00497549	intron-variant	RNF213	GRCh38.p7	17:80291583	ATAACTAAAATTTCC[A/G]GGGTAGGAATTTTGG	57674
rs763423137	snp	A/G	1.75708e-05	0.00296397	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376968	CCACTGGTACAGTAA[A/G]TGTTGGGGTCTAGAT	57674
rs763433391	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329544	GGATCTATGTTCCAT[C/T]GAGGCTGGGCATGTT	57674
rs763442462	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	RNF213	GRCh38.p7	17:80294893	TGGGACACCATCAAC[C/T]TGAACAGCTTCTTCA	57674
rs763448668	snp	C/T	3.39887e-05	0.00412228	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288181	CAGGACGCTTCCATC[C/T]CCTCTGGGGGCAGAG	57674
rs763450195	snp	C/T	1.65187e-05	0.00287386	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374567	TCGAGTGCAAGCCAC[C/T]GGGCATTAAGACTGC	57674
rs763483479	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80262682	GCTCTGAATAGCCAT[C/G]TCAAAATTGACCACA	57674
rs763485861	snp	A/G	0.000349205	0.0132091	intron-variant	RNF213	GRCh38.p7	17:80273198	TCCTTCCTAACACTC[A/G]CTTCTCTCTGAGATC	57674
rs763491650	snp	C/T	6.58989e-05	0.00573978	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367795	CGGGCCTTTTGAGGC[C/T]GTGATGCGCACTCTC	57674
rs763498811	snp	C/G	1.66946e-05	0.00288912	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379765	AACTTTGGGGTGTTG[C/G]GCTGTTTTTATTCCA	57674
rs763525816	snp	C/T	1.65663e-05	0.002878	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353572	AGACGGAGGCCAGCA[C/T]ATCAGGGGAGGTGGC	57674
rs763532099	in-del	-/GT			intron-variant	RNF213	GRCh38.p7	17:80323980	AAATTGTGTGTGCGT[-/GT]GTGTGTGTGTGTGTG	57674
rs763539118	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379406	AAATTGTCTCACTTA[C/T]TTAAAAAACAGTTCC	57674
rs763544047	snp	C/T	1.648e-05	0.0028705	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374490	CCCAGGCCAGATGGA[C/T]AGGTACCTGGTGTAC	57674
rs763575627	snp	C/G	3.31554e-05	0.00407144	missense	RNF213	GRCh38.p7	17:80263763	GAGAGGCTGCCTCCT[C/G]CAGCCCCCATAGCAG	57674
rs763580826	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80331724	AATGCAATTTATGTT[C/G]TGTCATTGGAGTGGG	57674
rs763592605	snp	A/G	0.000187683	0.00968536	intron-variant	RNF213	GRCh38.p7	17:80289619	AAAAAGAAAATGTGG[A/G]GGCCGGCCTTCAAGG	57674
rs763594229	snp	C/T	1.64746e-05	0.00287002	missense	RNF213	GRCh38.p7	17:80344981	TCCTGGTCAGAGCTT[C/T]GGAACTTTGCTCGGT	57674
rs763617593	snp	A/G	6.58913e-05	0.00573945	missense	RNF213	GRCh38.p7	17:80294797	AACCACATCACAGAC[A/G]GGCCGAGGAAGGACC	57674
rs763625430	snp	C/G	3.29478e-05	0.00405867	missense	RNF213	GRCh38.p7	17:80306395	ACCTGGGTCGTTTTC[C/G]TGCTCATATCCTGGA	57674
rs763631636	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380637	GCTGAGAATGCGGTC[A/G]GGTCTGGTCCACCGG	57674
rs763644147	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383924	TCTGGCATTTCCTGC[A/G]GAAGGTATGTCTGGC	57674
rs763673497	snp	A/G	0.000280101	0.011831	intron-variant	RNF213	GRCh38.p7	17:80349740	TTTCCTTGAAGTCTG[A/G]CAAGTAATTTGCATT	57674
rs763681662	snp	A/G	8.23744e-05	0.0064172	missense	RNF213	GRCh38.p7	17:80345945	AGGAGATGATCTGCC[A/G]TTTGGAGTCAGCTGG	57674
rs763691569	snp	A/G	4.94238e-05	0.00497086	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383884	ATTGTGGAACAGAAA[A/G]ATGGCAAAGAAAGAG	57674
rs763694406	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80262975	TGAGGCTTCTTACTG[C/G]GGAGGGAGAGAGTCA	57674
rs763699377	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385877	CACCATGTTGCCCAG[A/G]CTGGTCTCAAACTCC	57674
rs763701904	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80301576	ATTAGGGAAATGCAA[A/G]TCAAAACCACAATGA	57674
rs763705104	snp	A/G	1.6486e-05	0.00287102	missense	RNF213	GRCh38.p7	17:80345806	TTTGATGAAGCCAAC[A/G]CAACGGAAGCTATAA	57674
rs763717754	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272714	GTGAGTGTGGGGCTG[A/G]CAGAGTGGGTGCTCC	57674
rs763727729	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389071	AGAGAGTTGGCCCCC[C/T]GCATGTGGCTTGGGC	57674
rs763735720	snp	A/G	3.29755e-05	0.00406038	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380849	CAAGGCAGACAGAAC[A/G]CAGACCGGCCACGTG	57674
rs763735986	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80349834	AATCAGAGGTCACAG[A/G]CAGGGCTCCGAAACC	57674
rs763746779	snp	C/T	3.29457e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383797	CTGCCCCACCTGCCC[C/T]GGAAAAGTGTGGTCC	57674
rs763755023	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80325218	GTTTGCGGGAGTGCT[A/G]GGAACATCAGCTCAG	57674
rs763763957	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317488	GGACAGAGAAGAACA[A/G]GGGCCCAGGATCTCA	57674
rs763773828	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352631	TCACTAACTGTGATA[C/T]AGCAAATACAACAAT	57674
rs763805489	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80272162	GGTGGCATGCACCTG[C/T]AATCCCAGCTACTTG	57674
rs763813630	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388360	CCTAGCGCCTCCTGT[G/T]GCGAAGCAGGCCACG	57674
rs763828869	in-del	-/AT	1.64792e-05	0.00287042	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380897	GAGAGACGTGGTGAC[-/AT]GTGACCGAGGGCTGC	57674
rs763836806	snp	A/G			missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353555	CCATGAGGAGGCGAT[A/G]GAGACGGAGGCCAGC	57674
rs763845255	in-del	-/G	1.71743e-05	0.00293033	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385493	GGTTTGGCCCTTTCA[-/G]GGGGTTGCTATCATA	57674
rs763852386	snp	A/G	1.73153e-05	0.00294233	intron-variant	RNF213	GRCh38.p7	17:80343082	CAAAGTGCTAGGATT[A/G]CAGGTGTGAGCCACC	57674
rs763858520	snp	C/G	0.000115533	0.00759957	missense	RNF213	GRCh38.p7	17:80332269	TTGCTGAGTGAGCCC[C/G]AAGAAGAATCAGAAA	57674
rs763887166	snp	G/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80258908	CTGCTGCAGCAGCTG[G/T]TAGGGGCAGACTGTG	57674
rs763889016	snp	C/T	3.45746e-05	0.00415765	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382941	CTGCTGTGTTCTTTG[C/T]GCCTTGGGTAACCTA	57674
rs763891430	snp	C/G/T			intron-variant	RNF213	GRCh38.p7	17:80284220	AAAAAAAAAATTAGC[C/G/T]GGGCATGATGGCAGG	57674
rs763904159	snp	C/T	5.63269e-05	0.00530663	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287930	CTTTGCTTTCAAACC[C/T]GTGGCCTCAGGACAC	57674
rs763908472	snp	A/G	1.65441e-05	0.00287607	splice-donor-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354577	GGCGGGCACATTCAG[A/G]TACTGTGACTAAAGG	57674
rs763915652	snp	A/G/T	3.29719e-05	0.00406018	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390108	CAGACTGGCCTAGAC[A/G/T]CCTTCCTGCTAGAGC	57674
rs763921337	snp	A/G	1.66333e-05	0.00288381	missense	RNF213	GRCh38.p7	17:80346517	GATGAAATAACACGG[A/G]CACAGGATCTTTTTC	57674
rs763930338	in-del	-/TGG			intron-variant	RNF213	GRCh38.p7	17:80277692	CCGATGGGTTGTCTC[-/TGG]TGATGAGTTTACAGG	57674
rs763931181	in-del	-/TT	1.64732e-05	0.0028699	frameshift-variant	RNF213	GRCh38.p7	17:80290623	ACGCCATCATCTCTC[-/TT]CATTTCCCATTCAAT	57674
rs763931649	snp	A/G	1.65089e-05	0.00287301	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352920	ACAAAGACAGTTGTG[A/G]GTGGCTTCACTCTTC	57674
rs763934975	snp	G/T	1.65446e-05	0.00287612	missense	RNF213	GRCh38.p7	17:80298361	TGCCAAAGATGCATG[G/T]ACACAAGGACGTACA	57674
rs763938536	snp	A/G	1.65902e-05	0.00288008	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389340	AGACATCCTGCAAAT[A/G]GGTGATCAGACGATT	57674
rs763939503	snp	A/G	3.30087e-05	0.00406242	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363146	TAGGAAACTGAAAGC[A/G]GCGTCAGAAGCGCCC	57674
rs763939891	snp	A/C	1.64876e-05	0.00287116	synonymous-codon	RNF213	GRCh38.p7	17:80347578	GGACCAAGAGTACAC[A/C]CAGCTCTGCAGAAAC	57674
rs763957997	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80297449	GTGAGACTTCATCTC[-/A]AAAAAAAAAAAAAAG	57674
rs763965143	snp	A/G	0.000131813	0.00811721	intron-variant	RNF213	GRCh38.p7	17:80308990	CCTAAATCCTTGCCG[A/G]GATTTCTCTTAACTC	57674
rs763966774	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80336675	CTCTGAATGGTTGTA[A/G]TTGTCATTTTATTCT	57674
rs763973660	snp	G/T	9.88419e-05	0.00702931	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376292	AATGTTAAGTTTTTT[G/T]CCTGTCAGCAATGTG	57674
rs763976631	snp	A/G	1.65048e-05	0.00287265	missense	RNF213	GRCh38.p7	17:80298445	CACAAGGATGCCTGG[A/G]GACAGCCTGAGGACA	57674
rs763977220	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259424	GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC	57674
rs763981460	snp	C/G	0.000203169	0.0100769	intron-variant	RNF213	GRCh38.p7	17:80332658	GCTGGGGACTGTGGG[C/G]GTTTGGAGGGGCGTC	57674
rs763984219	snp	A/G	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80309136	GCCTTATCTGCCGAG[A/G]TTGTCTGCAGAATGA	57674
rs763986913	snp	C/T	0.00222676	0.0332929	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355302	ATCTGCAGGAGGGAA[C/T]GTGAGGAAGAAGCGG	57674
rs763992670	snp	A/T	2.1972e-05	0.00331444	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363070	ATTTTTGTAATTTAA[A/T]AATATATTCTAAAAG	57674
rs763996463	snp	C/T	4.96545e-05	0.00498245	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364601	GGATCCACCCTTTTC[C/T]GAAAGGAAGAACAGC	57674
rs764008390	snp	G/T	1.81473e-05	0.0030122	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385663	AAGCGTTCCAGGAGA[G/T]CCTCGTCTGAAAGCT	57674
rs764012514	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80345098	TTCGTGGTGACCTTC[A/G]TGATCTTTATGGCAA	57674
rs764043790	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374203	CGGTGCGCCGCAAAC[A/G]GAGGAAGCAAGCACC	57674
rs764044027	in-del	-/G	5.03893e-05	0.00501917	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363698	GTGGCTACAGTTGGT[-/G]AAGAATCTTTCCATG	57674
rs764074862	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367580	GCATAATCACAAAAC[A/G]AGCATTCAGAGTTCA	57674
rs764077430	snp	A/G	0.000317044	0.0125866	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373050	AGAACGACTGGCACC[A/G]GGTGTACCTGGTGCG	57674
rs764078893	snp	G/T	1.8718e-05	0.00305919	intron-variant	RNF213	GRCh38.p7	17:80306514	GGCTTAGCAAAAGCA[G/T]ACTAGATAACTAAAC	57674
rs764090790	in-del	-/A	1.64757e-05	0.00287012	frameshift-variant	RNF213	GRCh38.p7	17:80307191	GACTCCTGGACACTT[-/A]ACCGGGACAAGTAAG	57674
rs764097480	snp	G/T	4.13702e-05	0.0045479	intron-variant	RNF213	GRCh38.p7	17:80317298	AAAAGTTTGGGGGCA[G/T]TCTTTTCAGGGCGTG	57674
rs764108900	snp	C/T	1.64836e-05	0.0028708	missense	RNF213	GRCh38.p7	17:80345545	AATATGCTTAAAATC[C/T]TTGCCATCGAGATGC	57674
rs764112639	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80291706	TAAATACATTCCTTA[C/T]AAGTACGTCATTTAT	57674
rs764115317	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80267989	CACTTCCGGCTAATA[C/T]TGTATTTTTTATTAG	57674
rs764127762	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80335323	CGTTGGCAGAGGAGA[C/G]AGGAAGAGGCAGAGG	57674
rs764132745	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382677	GCTGAGACGGCTGGC[A/G]GTAGCCTGGGCCACT	57674
rs764134758	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357595	TTATTTTTTCCAAAT[A/G]AATCGTCATAATTTT	57674
rs764168841	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80278481	AGCTTGGCAGGGTGC[C/T]GTGAGCCTGGCAGGG	57674
rs764187396	snp	A/G	1.71549e-05	0.00292868	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363758	CATGCAAGGCAGCGG[A/G]AGCCTGGCCCAGGCT	57674
rs764191111	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383601	CAGACACCCACTGGT[A/G]GAGTTACTGGGTGTT	57674
rs764192335	snp	A/G	3.41618e-05	0.00413276	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288287	AGCTCCTGTTGCCTG[A/G]GTCAAAAGGAGGCAG	57674
rs764201378	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358589	TCAACTTCAGAGCAA[C/G]GTTGACATGGGTGCT	57674
rs764204992	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80266967	ATTAAAAGTGCCCCC[A/C]GCACTTTGGGAGGCT	57674
rs764214281	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391109	ATACCAATGTATAAA[G/T]AGTGTATGAGAATAC	57674
rs764238897	snp	A/T	1.68267e-05	0.00290053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390245	CACAATGTTGTGCTG[A/T]CTCTCCTGTGATCTT	57674
rs764250282	in-del	-/CTGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356508	AGGGCCAGCAGCACC[-/CTGA]CTACCTCGATTCACC	57674
rs764264107	snp	A/C	4.94531e-05	0.00497234	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385030	ACTGGGTGGTCTTCC[A/C]TTCTCCAGGAAGCAG	57674
rs764265371	snp	C/G	2.02723e-05	0.00318366	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363815	AGGAGCCCTCACCCA[C/G]TGCTTCATCTGGCGC	57674
rs764275188	snp	A/G	1.6916e-05	0.00290822	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383074	CCTGAACTGGAGGTA[A/G]GCAGTAAGTGCTGAC	57674
rs764290638	snp	A/G	1.67427e-05	0.00289328	missense	RNF213	GRCh38.p7	17:80347151	CCTTTGCCAAAGCCT[A/G]CGAAACGGTGTGTAA	57674
rs764308928	snp	A/C	1.66161e-05	0.00288232	missense	RNF213	GRCh38.p7	17:80347052	CACGTGGCAGCCCCA[A/C]CGAGACAGAGCTCAT	57674
rs764309309	snp	A/G	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80345587	GGGATCCCGGTTATC[A/G]TCATGGGAGAAACTG	57674
rs764312055	snp	C/G	0.000115814	0.0076088	missense	RNF213	GRCh38.p7	17:80339752	TGCCTTCCTGCCCGA[C/G]TGCCTCGACCTAGAG	57674
rs764317680	snp	A/C	5.6906e-05	0.00533383	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376988	GGGGTCTAGATGACC[A/C]CACACTCCTTTGAGC	57674
rs764323267	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80307811	TGTCTGGGCCTCCCA[A/C]AGTGCTGGGATTACA	57674
rs764327290	snp	C/G	1.65138e-05	0.00287343	missense	RNF213	GRCh38.p7	17:80348128	AACTGCGCTACGCCC[C/G]ATGCCGTGGTCCGGC	57674
rs764338917	snp	C/G	0.00045683	0.0151065	missense	RNF213	GRCh38.p7	17:80327876	GGCTGATAGCTGTTG[C/G]CGACTCTGTGTTGAC	57674
rs764344418	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80274638	GGTGTCTGTGGGGGG[A/T]GTGGGGTGAGTGTGT	57674
rs764350518	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329819	TTGGGTGACAGAGTG[A/G]GACCCTGTCTCAAAA	57674
rs764350752	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80276288	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	57674
rs764357406	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391243	GTTTTTTATATTTAT[C/T]ACCCATTTGTATATC	57674
rs764358749	in-del	-/AAT	3.13298e-05	0.00395777	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371852	TCTGAGAGAACCAGG[-/AAT]AATATTTCTCTTTCT	57674
rs764389862	snp	A/G	2.59434e-05	0.00360153	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386897	GAGCCTCAAGGTAGG[A/G]CTGACTCCTGCCACT	57674
rs764432033	snp	G/T	3.34437e-05	0.0040891	intron-variant	RNF213	GRCh38.p7	17:80344059	CGTGGGGGGCTCTTG[G/T]GTTCTTTCTGGTCTT	57674
rs764445482	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80339074	AGGGAGGCCTTGTGA[A/G]CGCAGATCATGCAGT	57674
rs764448109	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80298117	TGTTGTGGGGATTCG[A/G]TGAGGGCCTGCAAAG	57674
rs764454327	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328952	CACAGAATTACATTT[C/T]CTGTCAGATGCTGTT	57674
rs764487227	snp	A/C	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80290530	ATGGCAGGTGGACAG[A/C]TCTCACGGGAATCAG	57674
rs764488270	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270143	ATGTGAGTGGCAGCT[C/T]GTGCCCTGCGCATGC	57674
rs764506172	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368227	AGAAATATAAACTCT[A/C]TTAACCTTCATTTGG	57674
rs764527769	snp	A/C	1.64781e-05	0.00287033	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381538	CACTCTGTTCCGTTG[A/C]CCCCACAGGCTCTGA	57674
rs764535486	in-del	-/TCTG			intron-variant	RNF213	GRCh38.p7	17:80268642	CCATCCATCCGTTTA[-/TCTG]TCTATCTATCTGTCA	57674
rs764535738	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80311694	ACTCTCGGGCAGCCC[C/T]GCCCAGCAGCAGCCT	57674
rs764537332	snp	C/G	1.86583e-05	0.00305431	intron-variant	RNF213	GRCh38.p7	17:80350262	TTTCCATTTTTTTAA[C/G]ACAGAGAACTCACTT	57674
rs764539214	snp	C/T	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80345218	GCGCCCTTCTCCCTC[C/T]GGAAGAGGTGGGAGT	57674
rs764555324	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377127	GACGAATGGCTTGAA[A/G]GAGCTGGCACTCCGC	57674
rs764585188	snp	C/G	3.3222e-05	0.00407553	synonymous-codon	RNF213	GRCh38.p7	17:80295583	CCTGTGGCAACATCT[C/G]AAAAAACACGTGGTA	57674
rs764586150	snp	A/C/G/T	0.000100537	0.00708946	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354024	CCACCAACAGGTGTC[A/C/G/T]ATCCTGGACACCACC	57674
rs764588588	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394925	GATCTGCATTCCGAC[C/T]GCCTATGAACGGGTG	57674
rs764593065	in-del	-/G	1.64742e-05	0.00286999	frameshift-variant	RNF213	GRCh38.p7	17:80346173	ATGAAAACGGGACTC[-/G]CGTGATCACAGAAGT	57674
rs764593834	snp	G/T	1.64749e-05	0.00287005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376459	GACAGAAATGGCCAT[G/T]CATGCTGCAGCCGTC	57674
rs764602231	snp	A/G	3.29457e-05	0.00405854	missense	RNF213	GRCh38.p7	17:80345278	GACGACCACACAACC[A/G]TGACATTCATCGGCT	57674
rs764615402	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353759	GGGAGCTAGAGGAGT[C/T]GCCGCCGCTGTGCAG	57674
rs764628653	snp	C/T	4.94417e-05	0.00497176	synonymous-codon	RNF213	GRCh38.p7	17:80347728	GAAGTACGTGGACCT[C/T]GGTCTGGGGACCCAC	57674
rs764631143	snp	A/G	3.39547e-05	0.00412022	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367698	TCGCCCGGCCTGGCC[A/G]CCCTCAGCCCTCCCC	57674
rs764637426	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80333555	AAAAATTAGCCGGGT[A/G]TGGTGTCAGGTGCCT	57674
rs764649476	snp	A/G	0.000114436	0.0075634	intron-variant	RNF213	GRCh38.p7	17:80324991	AAACAAACTAATGAA[A/G]AACTTCTAAATGTCC	57674
rs764658196	snp	A/C	1.98533e-05	0.00315059	missense	RNF213	GRCh38.p7	17:80289805	GAAGGAGCAAAAAAA[A/C]CAGGAAGCAGATGTC	57674
rs764662888	snp	C/T	5.19561e-05	0.0050966	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351644	TTTTTGTGTGTGTGT[C/T]TGTTTTTAAAATAGG	57674
rs764664395	snp	C/T	1.64746e-05	0.00287002	missense	RNF213	GRCh38.p7	17:80349854	GCTCCGAAACCCACA[C/T]TCCTGTGGCTGCAGC	57674
rs764667087	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389908	TGAACAGCTGCTGCG[A/G]CTGCACAAAGTAAGT	57674
rs764672092	snp	C/G	4.66277e-05	0.00482821	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287848	AAGAAGAAAAAGAAG[C/G]GGAACAAGTCCGCTT	57674
rs764681341	snp	A/G	1.64879e-05	0.00287118	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386399	AATGAAATTGTCTAC[A/G]CCGTGGAAAAACTCT	57674
rs764690017	snp	A/G	1.65493e-05	0.00287652	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385006	TTTTTTAGGTAAATA[A/G]AAATTGTTACTGGGT	57674
rs764691900	in-del	-/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387673	TGCCGGATGGACCTG[-/C]CTGGCCTCTCATGGC	57674
rs764703963	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80350223	TGTAGCCTTTATGTT[C/T]CCCATCACTTTGGGG	57674
rs764716167	snp	C/T	3.32397e-05	0.00407661	synonymous-codon	RNF213	GRCh38.p7	17:80350373	AGATGGAATCCGTAG[C/T]GCCCAGCTCATTGCC	57674
rs764722167	snp	A/G	1.64879e-05	0.00287118	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389810	AGCCCCCACTCAGGA[A/G]TTCTATTCCTTCTGC	57674
rs764734820	snp	C/T	1.71941e-05	0.00293202	intron-variant	RNF213	GRCh38.p7	17:80343099	AGGTGTGAGCCACCA[C/T]TCCCAGCCCTAATTT	57674
rs764738198	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277876	GAGACAGCGAGCTGC[A/G]TGGCCAGCCTCACCC	57674
rs764762202	snp	A/G	1.64882e-05	0.00287121	missense	RNF213	GRCh38.p7	17:80289710	GCTGAAGAAAAAGTC[A/G]GTAAGAATGAACAAG	57674
rs764764818	in-del	-/CT	1.64933e-05	0.00287165	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386411	TACGCCGTGGAAAAA[-/CT]CTCCAAGGAAAACAA	57674
rs764766249	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265367	GCTCCACTTCTATTA[A/G]TAATAGTGCGGAGAG	57674
rs764768461	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363864	CCAAGTGCCAGGCAT[C/G]TCCATGAGAAGACGG	57674
rs764813257	snp	C/T	1.65441e-05	0.00287607	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319468	CGCCAAGGGCAATGG[C/T]GCTGAAATCTAGTTC	57674
rs764823009	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80345137	GCCACACCATCACTC[C/T]ACACCTCTGACCAAA	57674
rs764824345	snp	C/G	4.94466e-05	0.00497201	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380921	AGGGCTGCCCCCAGT[C/G]GTCTTCCTCCTTATC	57674
rs764834830	snp	A/C	6.58957e-05	0.00573964	synonymous-codon	RNF213	GRCh38.p7	17:80309154	GTCTGCAGAATGATT[A/C]GACTTCTATCTCTGG	57674
rs764836730	snp	A/G	0.000115305	0.00759205	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376303	TTTTTCCTGTCAGCA[A/G]TGTGAAGCTGTGAGC	57674
rs764837983	snp	A/T	5.02989e-05	0.00501467	intron-variant	RNF213	GRCh38.p7	17:80295018	GGTATCAGGCTTGCC[A/T]CCAGCTGCTCTACCT	57674
rs764839860	snp	A/G	0.000115311	0.00759224	missense	RNF213	GRCh38.p7	17:80344994	TTCGGAACTTTGCTC[A/G]GTTCCTGAATTATCA	57674
rs764843249	snp	A/G	1.64947e-05	0.00287177	intron-variant	RNF213	GRCh38.p7	17:80309217	CCCGGGATAGGTGCG[A/G]AATTTCAAGCAGCCT	57674
rs764856729	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80264124	TTTGTCGGGGTCTTT[G/T]CTGGAGGTTCCTGCT	57674
rs764864696	snp	A/C	1.64841e-05	0.00287085	missense	RNF213	GRCh38.p7	17:80347597	CTCTGCAGAAACATC[A/C]ATCGTGTGAAGATCT	57674
rs764865527	snp	G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394414	CCAAGACATAAAAAC[G/T]AGGACTCAGAGCACA	57674
rs764865975	snp	A/C/G	3.29947e-05	0.00406159	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363149	GAAACTGAAAGCGGC[A/C/G]TCAGAAGCGCCCGAG	57674
rs764869637	in-del	-/T/TT	0.313895	0.280003	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351664	TTAAAATAGGTATTC[-/T/TT]TTTTTTTTTTCTTTA	57674
rs764873221	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80339575	CATCAAAAGCAACTG[C/T]ACCCTGAGGGATGTC	57674
rs764874640	snp	A/G/T	0.000116761	0.00763982	missense	RNF213	GRCh38.p7	17:80332399	CCCTTGCAGAGATTG[A/G/T]TGTCATCTTCAAGGA	57674
rs764881147	snp	C/G	1.64901e-05	0.00287137	synonymous-codon	RNF213	GRCh38.p7	17:80347491	AAACTACGTGGCACT[C/G]CAGATCCTGCAGCAG	57674
rs764881763	snp	C/T	1.64787e-05	0.00287038	missense	RNF213	GRCh38.p7	17:80346071	GCCTGATTCCTCTGG[C/T]GTGGGACTTTGGACA	57674
rs764896683	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380726	GCAAGTACTCTTCAC[A/G]TAACTCTCTTCTCAG	57674
rs764917009	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80310555	CTGCACCCAGCACAA[-/T]TTTTTTTTTTTTTTG	57674
rs764921190	snp	C/G	1.68018e-05	0.00289838	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373106	GAGTTCGTGCAGGGC[C/G]TCTCCAAGCCCGGCC	57674
rs764924271	snp	C/T	3.34806e-05	0.00409136	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287936	TTTCAAACCCGTGGC[C/T]TCAGGACACAGCCCT	57674
rs764935286	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80317617	GGAGCACGTGAGTGA[G/T]TGTGGCATCTGGCCA	57674
rs764946551	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80263150	CAGTGCAGAGTGGCG[C/T]GCTTTGTGGATGGCA	57674
rs764961332	in-del	-/G	3.39628e-05	0.00412071	intron-variant	RNF213	GRCh38.p7	17:80291874	CTCCGGAGTGCAGGT[-/G]GCCAATCCCGCGGTA	57674
rs764982473	snp	A/G	2.42827e-05	0.00348436	intron-variant	RNF213	GRCh38.p7	17:80317327	TGAAGGCAAGCTGGA[A/G]AACCCCAGACCATTA	57674
rs764986178	in-del	-/GG	1.65e-05	0.00287224	intron-variant	RNF213	GRCh38.p7	17:80307240	CTCTCCCTCACATGC[-/GG]CCCCCGGGGGCTTCC	57674
rs765016715	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80344565	AAGCTACATATTTTC[A/C]GTGCGTTTTTCATAA	57674
rs765019511	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377773	ACAGCTTGTCCCAAC[A/G]GCCATCCTTGCTCCG	57674
rs765028715	snp	A/G	0.000297481	0.0121923	missense	RNF213	GRCh38.p7	17:80298388	TACACCTGGCTGGGC[A/G]CCCTGCCTGTCCTGC	57674
rs765044536	snp	A/G	0.000115307	0.00759211	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389886	AGTTCCTGTCTGCTC[A/G]TAAGTCTGAACAGCT	57674
rs765059046	snp	C/G	1.64811e-05	0.00287059	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369526	TGAAAAGCATGCCCG[C/G]TTCCGGCAGATGTGC	57674
rs765061480	snp	C/T	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80291719	TACAAGTACGTCATT[C/T]ATAATGGGGAATCTT	57674
rs765070483	snp	C/T	0.000114633	0.00756989	intron-variant	RNF213	GRCh38.p7	17:80334092	CAGTCCACAGTAGAG[C/T]TTTTTCTTGCAGACT	57674
rs765084250	snp	A/G	1.64844e-05	0.00287087	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358316	AAGCGGGTCCAAGGT[A/G]CTGTCACCCCTCTGC	57674
rs765086276	snp	G/T	1.65018e-05	0.00287239	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352941	TTCACTCTTCACAGG[G/T]CTGTGGCAGTCTGTC	57674
rs765089503	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80261688	GCCTGGGGCTCTCTC[-/TT]GTGTCTTCCGGCCCC	57674
rs765089967	snp	A/C	3.29734e-05	0.00406025	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354448	TTGTACAGCCTCTTT[A/C]TTGCGGGTATCCAAG	57674
rs765095724	snp	A/G	1.6486e-05	0.00287102	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363237	CAGAACTTTTCCAGA[A/G]TCCTGACCATCTACC	57674
rs765100848	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80327196	AAGATTCTGTGTATT[C/G]TATTTAAAAAATATA	57674
rs765116016	snp	C/G/T	5.00474e-05	0.00500216	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373060	GCACCGGGTGTACCT[C/G/T]GTGCGGAAGCTCAGC	57674
rs765117764	snp	C/G	1.66829e-05	0.00288811	missense	RNF213	GRCh38.p7	17:80346621	CTGCATCGAGCTGAA[C/G]ATTCCCCTCTTCCTG	57674
rs765128580	snp	C/G	1.66479e-05	0.00288508	missense	RNF213	GRCh38.p7	17:80346526	ACACGGGCACAGGAT[C/G]TTTTTCTGGACGGCG	57674
rs765128607	snp	C/G	1.71243e-05	0.00292607	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382959	CTTGGGTAACCTACA[C/G]ATTTGGAGTTTTTTT	57674
rs765129620	snp	G/T	1.66399e-05	0.00288438	missense	RNF213	GRCh38.p7	17:80273290	CTCGGAGGGTGAAAT[G/T]GAGTGTGGGCAGGAG	57674
rs765139436	snp	C/T	0.000934492	0.0215957	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355324	AAGAAGCGGGGTGAA[C/T]GGTAATGGGGGCTTA	57674
rs765153395	snp	C/G	1.65045e-05	0.00287263	missense	RNF213	GRCh38.p7	17:80298454	GCCTGGAGACAGCCT[C/G]AGGACACCTGGGCCG	57674
rs765164264	in-del	-/TTTCT	3.32878e-05	0.00407956	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372010	TCTCTCTTCCCTGAA[-/TTTCT]TTTCTTTTGGAAACT	57674
rs765178941	snp	A/G	1.67657e-05	0.00289527	missense	RNF213	GRCh38.p7	17:80347153	TTTGCCAAAGCCTAC[A/G]AAACGGTGTGTAAGC	57674
rs765185020	snp	A/C	1.66707e-05	0.00288705	missense	RNF213	GRCh38.p7	17:80273361	ACAGTTGGCAAGAAA[A/C]CCCCGAGGAGCCCTG	57674
rs765204565	snp	A/C	1.64779e-05	0.00287031	intron-variant	RNF213	GRCh38.p7	17:80344650	AAAGTCTTCTTGTAA[A/C]CATTTCATTAATGTC	57674
rs765216006	snp	C/T	1.66001e-05	0.00288094	synonymous-codon	RNF213	GRCh38.p7	17:80295592	ACATCTGAAAAAACA[C/T]GTGGTACCATTGCCG	57674
rs765227438	snp	A/C/T	3.45192e-05	0.00415435	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363766	GCAGCGGGAGCCTGG[A/C/T]CCAGGCTGTCATCAG	57674
rs765229293	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378321	CACGTGTAGGCTGTG[C/T]GCCATGGGGGAAGAA	57674
rs765236391	snp	A/C/T	3.29491e-05	0.00405877	synonymous-codon, stop-gained	RNF213	GRCh38.p7	17:80307176	TTAGAAATGCTGTTG[A/C/T]GACTCCTGGACACTT	57674
rs765247294	snp	G/T	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80345606	TGGGAGAAACTGGCT[G/T]TGGGAAAACCAGGCT	57674
rs765260386	in-del	-/C	1.6477e-05	0.00287024	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374432	TCCTCCCATTGTTCA[-/C]CCCCCAACTAACCTC	57674
rs765276592	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80336777	GGCATGGTGGTGTGC[A/G]CCTGTAATCCCAGCT	57674
rs765304353	snp	A/G	1.65108e-05	0.00287317	missense	RNF213	GRCh38.p7	17:80348203	CAGGAGTACTTTCAC[A/G]GACAGAGGCACAACT	57674
rs765317317	snp	A/G/T	4.96071e-05	0.00498011	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353040	CAGCCAGCTGTTCGC[A/G/T]CCCGGAGACTTGCCT	57674
rs765327318	snp	A/G	1.65586e-05	0.00287733	synonymous-codon	RNF213	GRCh38.p7	17:80291823	TTCACTTCTGGGCTC[A/G]GGAGGTAAGTCGTGG	57674
rs765332800	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375789	CCAAAGCCAGCAGTC[A/G]GCCTACTTCCTGTTA	57674
rs765334870	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80349467	ATTTGTGCTGAGCCC[C/T]AAGGGATCATGAGAA	57674
rs765339858	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384320	CCTGTGCCTAAGCAT[C/T]GAGGCGTACGTGGAA	57674
rs765343052	snp	C/T	1.65018e-05	0.00287239	intron-variant	RNF213	GRCh38.p7	17:80307242	CTCCCTCACATGCGG[C/T]CCCCGGGGGCTTCCT	57674
rs765346204	in-del	-/TAGTAGCTGGGA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391396	CTGCCTTAGCCTCCC[-/TAGTAGCTGGGA]TTACAGGTGCCAACC	57674
rs765347533	snp	A/G			splice-acceptor-variant	RNF213	GRCh38.p7	17:80291627	TCCTGTTCATTCACA[A/G]AGACTTGGGTCATGA	57674
rs765365184	snp	C/T	3.30093e-05	0.00406246	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354405	CCAACAGCTCAGCCA[C/T]GGCCATGCTGAACGT	57674
rs765379293	snp	C/T	7.27114e-05	0.00602913	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389077	TTGGCCCCCCGCATG[C/T]GGCTTGGGCAGTGAA	57674
rs765380602	snp	A/G	1.9799e-05	0.00314629	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372527	GTTCCTCAGGATTCA[A/G]TACTTGAGAAGACCA	57674
rs765385710	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358648	GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	57674
rs765390552	snp	C/T	3.64598e-05	0.00426949	missense	RNF213	GRCh38.p7	17:80340015	TGCGCCGCTGCCTGA[C/T]CCTGGGCTCCCTGGG	57674
rs765395101	snp	C/T	1.66524e-05	0.00288547	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381036	TTAAGAACCTGCTTT[C/T]GCTTCTTCCCAGGGA	57674
rs765418314	snp	C/G	8.25621e-05	0.0064245	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388636	ACTCTGGTGTACAGA[C/G]ACGACTGGAACTATG	57674
rs765430996	snp	A/G	1.66239e-05	0.00288299	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375716	TCAAAAAAAAAAGAT[A/G]TGTTGAGCTTTTAAA	57674
rs765431873	snp	C/G	1.64765e-05	0.00287019	synonymous-codon	RNF213	GRCh38.p7	17:80346270	CGTGGAGCGCTGTGT[C/G]AAAGTTTTCAGGTGG	57674
rs765433958	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393159	CTAATTTTTGTATTT[C/T]TGCTAGAGACAGGGT	57674
rs765449728	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80348378	TCTTCCCCAGGCAGC[A/G]GTTAGGGATCCTGCA	57674
rs765456028	snp	C/T	1.87036e-05	0.00305802	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351670	ATAGGTATTCTTTTT[C/T]TTTTCTTTAAATAGG	57674
rs765456882	snp	C/T	0.000114123	0.00755303	missense	RNF213	GRCh38.p7	17:80327900	TGTTGACGAAAGTTG[C/T]TGGTGACCTCCTAAG	57674
rs765465822	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	RNF213	GRCh38.p7	17:80290687	AGAAGAATTTGGGGA[A/G]TCAAAATGGGACAGC	57674
rs765468865	snp	C/T	5.13185e-05	0.00506523	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363576	CGGTGGGAGGGGCAC[C/T]GCTCAGCCACGCCCT	57674
rs765476880	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80344771	ATGGAGCTGAGTGCC[C/T]TGAGGAGTGACACAG	57674
rs765483727	snp	A/G	3.29544e-05	0.00405908	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361807	CCAGCTCCATGGAGA[A/G]CCGCAGCAGGAACTT	57674
rs765486456	snp	C/G	1.67136e-05	0.00289076	missense	RNF213	GRCh38.p7	17:80350380	ATCCGTAGCGCCCAG[C/G]TCATTGCCTCAGCTA	57674
rs765498655	snp	C/T	1.70708e-05	0.00292149	synonymous-codon	RNF213	GRCh38.p7	17:80347257	TTCAAATAGAAAGCC[C/T]TCCCCGCAAGACATT	57674
rs765502583	snp	A/C	1.64738e-05	0.00286995	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385146	ATACAGCTCCATCAG[A/C]GGCTTCCTCAGCAAG	57674
rs765505418	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80307631	CTTGGCTCACTGCAA[A/C]CTCTGCTTCCCAGGT	57674
rs765511493	snp	C/T	3.29979e-05	0.00406175	synonymous-codon	RNF213	GRCh38.p7	17:80313164	ATACGTCAAGGAAAT[C/T]GAGGTAGGCATTTGG	57674
rs765525681	snp	C/G	3.29473e-05	0.00405864	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367917	TTTCACTTCTTCTGG[C/G]CAGTTTCTCTGCTTC	57674
rs765529563	snp	A/G	0.000114149	0.0075539	synonymous-codon	RNF213	GRCh38.p7	17:80328455	CCTGAAGATGTGTGG[A/G]AACGTGAAACATCTG	57674
rs765533410	snp	A/T	3.31521e-05	0.00407123	missense	RNF213	GRCh38.p7	17:80295653	GACTGCCCAGTGAGG[A/T]GTAAACTGAAAACAG	57674
rs765543315	snp	A/G	1.67773e-05	0.00289626	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354171	CGCGTGCCACGGTAT[A/G]AGCCTCCCCACCCCT	57674
rs765581843	snp	A/C	0.000149811	0.00865351	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376547	GCCACCATGGCGGTA[A/C]GAGTAGGCCACAATT	57674
rs765586935	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80350494	GTATAGTATCATAAT[-/C]AGTATAGAAATAAAA	57674
rs765587374	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379557	TGTTCATTTGCATGA[C/T]GGCATTTGTGCATAA	57674
rs765591142	snp	A/G	0.000115305	0.00759205	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389918	CTGCGGCTGCACAAA[A/G]TAAGTCTGGTCTCTT	57674
rs765593017	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329103	ACCCTGGGCTGCAGA[C/T]GTAGGGTGGAGTCTC	57674
rs765595595	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320156	CTTCAAAGAGAAACC[C/T]GGCCCCTTTAGCCAT	57674
rs765606032	snp	C/G	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80290550	ACGGGAATCAGATTT[C/G]TGTTTTGGTTTTCCA	57674
rs765609360	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357661	AATAGTTACATACAA[A/G]AATTATGCAGCCTTG	57674
rs765617490	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80330070	GAGATTTATTCAGAA[C/T]CAAACTTTCTGCTTA	57674
rs765630600	snp	C/G/T	3.2954e-05	0.00405908	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381546	TCCGTTGCCCCCACA[C/G/T]GCTCTGATAAACATC	57674
rs765640752	in-del	-/T	2.59872e-05	0.00360457	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351647	TTGTGTGTGTGTTTG[-/T]TTTTAAAATAGGTAT	57674
rs765643647	snp	G/T	2.15056e-05	0.00327908	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288074	TTGGCGACAGCCCCC[G/T]GCAGGCCCAGGCTTT	57674
rs765646049	snp	G/T	1.64991e-05	0.00287215	missense	RNF213	GRCh38.p7	17:80313091	TTGCTGCTACGAAAA[G/T]GTGGCTCCGAGAAGT	57674
rs765675931	snp	C/G	1.87296e-05	0.00306014	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376863	TATCTAGAGCTGTCT[C/G]TGTCTTCTTGTTTTT	57674
rs765683322	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80340460	GTGGAGAAACCGAGG[C/G]TCAGGGAGGGTGTGA	57674
rs765683325	snp	A/G	4.42429e-05	0.00470314	intron-variant	RNF213	GRCh38.p7	17:80343349	CCTCCAGCGTCAGCC[A/G]ATGGCCACATCAGTA	57674
rs765702782	snp	C/T	5.0647e-05	0.00503199	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372709	CAGAGCTGCAGATTT[C/T]CTCTCGGAGCCTGAG	57674
rs765705485	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80341527	CATAATGACATTTCA[A/G]TCAACAGCAGACCAC	57674
rs765708061	snp	C/G			missense	RNF213	GRCh38.p7	17:80313082	AAGGGACCCTTGCTG[C/G]TACGAAAAGGTGGCT	57674
rs765717922	snp	C/T	2.00938e-05	0.00316962	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373197	GGCAGCACACAAACA[C/T]GCACCCCCACAGCCC	57674
rs765735495	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80261757	GGCGCAGTGGCTAAT[A/G]CCTGTAATCCCAAAA	57674
rs765753313	snp	C/G	1.64757e-05	0.00287012	missense	RNF213	GRCh38.p7	17:80345365	AAGGTCATCAAGAGA[C/G]ACGTCATGACCAGGG	57674
rs765754518	snp	A/G	1.65326e-05	0.00287507	synonymous-codon	RNF213	GRCh38.p7	17:80263747	CTGCAGCCAGTGCGG[A/G]GAGAGGCTGCCTCCT	57674
rs765758786	snp	A/G	3.37115e-05	0.00410543	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358514	TCCCTGGGGAGAGAA[A/G]CTATCAGAACACAGC	57674
rs765760253	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366584	TTGAATTGGGTTGTT[A/G]ATTAACAAAGTTATT	57674
rs765761077	snp	C/G	1.65111e-05	0.0028732	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363266	CCCTCAGGTTCTCCA[C/G]AGCCTGATGGAAGCC	57674
rs765767649	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352334	CTGCGTGCACCTCTC[C/T]TGGACTGACTCTAGG	57674
rs765773812	snp	C/G	3.29598e-05	0.00405941	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358441	TATTTTCAGTGACAC[C/G]ATGCTTCTGAACATT	57674
rs765780042	snp	A/G	0.000625782	0.0176777	synonymous-codon	RNF213	GRCh38.p7	17:80306285	TATGAGAGAGAAGCA[A/G]CATTTGCTGAGCATA	57674
rs765789358	snp	C/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389997	AATGCTTCATTTGCT[C/G]TTCCGTCGTTTTAGG	57674
rs765811044	snp	C/T	3.30393e-05	0.0040643	missense	RNF213	GRCh38.p7	17:80347948	AATGTCAAAGCACAT[C/T]ATTTCCAGAAGAGGC	57674
rs765813521	snp	C/T	1.6759e-05	0.00289469	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363617	TCCCCAGACCCTGGA[C/T]GCATTTGCCGCAATG	57674
rs765815386	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325429	CTTGCTGTACCCTAG[C/T]GACTGTGCTGGGTCG	57674
rs765816785	snp	C/G	1.65594e-05	0.0028774	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288025	ACAGCCACCACGCCA[C/G]TGGAGGGTGACGGCC	57674
rs765833474	snp	A/G	6.63614e-05	0.00575989	synonymous-codon	RNF213	GRCh38.p7	17:80346780	CCCGCACTCCACCCC[A/G]CAGGGCATCATCAGC	57674
rs765840128	in-del	-/GAGGTGGCA	9.92228e-05	0.00704284	cds-indel, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353579	GCCAGCACATCAGGG[-/GAGGTGGCA]GAGGTGGCAGAGGTG	57674
rs765850300	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378231	GTCTTGATAGAATGG[C/G]AAGGTGTTGCCTGGA	57674
rs765850988	snp	G/T	1.65649e-05	0.00287788	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381017	TGCCAAACAATGGGC[G/T]CAGTTAAGAACCTGC	57674
rs765854038	snp	C/G	1.65255e-05	0.00287445	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386651	CCCTAGGCCCGCATG[C/G]CTGGCCTGGACGCTG	57674
rs765864801	snp	C/T	1.6484e-05	0.00287084	missense	RNF213	GRCh38.p7	17:80347622	AGATCTGCATGGAAA[C/T]AGGCAAGATGGTGTT	57674
rs765871777	snp	A/G	1.64974e-05	0.00287201	missense	RNF213	GRCh38.p7	17:80347858	GAGAAGCACTATCTG[A/G]ATATCAACACGGTGC	57674
rs765875131	in-del	-/TCTTTGCGGGG	1.64746e-05	0.00287002	intron-variant	RNF213	GRCh38.p7	17:80309004	GGGATTTCTCTTAAC[-/TCTTTGCGGGG]CAGGATTCCCGAGGA	57674
rs765905688	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80311947	GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	57674
rs765912590	snp	A/G	1.65053e-05	0.0028727	missense	RNF213	GRCh38.p7	17:80298469	GAGGACACCTGGGCC[A/G]CTCTGGAGGGACTCT	57674
rs765914009	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80280902	GGAGTAACAGAGGCG[C/T]GACCTGGGGATGCGC	57674
rs765920959	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80270755	CAGCCTGAAACCCAG[C/T]TCTCCTAGGCTTGCT	57674
rs765922110	in-del	-/ATC	1.64738e-05	0.00286995	cds-indel	RNF213	GRCh38.p7	17:80345584	TGTGGGATCCCGGTT[-/ATC]ATCATGGGAGAAACT	57674
rs765928818	snp	C/G	1.66161e-05	0.00288232	intron-variant	RNF213	GRCh38.p7	17:80312967	TCGCCGGGAACCTGA[C/G]TCCACAGCCGAGGAT	57674
rs765943105	snp	G/T	0.0015304	0.0276199	intron-variant	RNF213	GRCh38.p7	17:80290523	CATGCACATGGCAGG[G/T]GGACAGATCTCACGG	57674
rs765966177	snp	C/T	1.66114e-05	0.00288192	stop-gained	RNF213	GRCh38.p7	17:80343242	CAGGTGGATGAGAGC[C/T]GAGTCCTGGGCGCCC	57674
rs765977355	snp	A/G	1.64798e-05	0.00287047	synonymous-codon	RNF213	GRCh38.p7	17:80347713	CCACCTCGGCGGCCA[A/G]AAGTACGTGGACCTC	57674
rs765980348	snp	C/T	3.33728e-05	0.00408476	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373064	CGGGTGTACCTGGTG[C/T]GGAAGCTCAGCAGCC	57674
rs765987066	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318729	CAGGCGCCCGCCACC[A/G]CGCCCAGCTATATTT	57674
rs765991711	snp	A/C	4.94401e-05	0.00497168	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358326	AAGGTGCTGTCACCC[A/C]TCTGCTGGCGAGCAT	57674
rs765994197	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324021	AGAATTAAATTTTCT[A/G]TACATAAGATCATAT	57674
rs765999586	snp	A/C	1.69046e-05	0.00290723	intron-variant	RNF213	GRCh38.p7	17:80298549	GTGCTTATCTACATG[A/C]ATCTGGGAAGACTGA	57674
rs766002692	snp	C/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259833	TCGTGGGCAGTTGTC[C/G]GTTAGGAGGGGTGGC	57674
rs766003280	in-del	-/ATATT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385333	TTGAACCCCAAAAAC[-/ATATT]AGAAGCTTTCGCCAC	57674
rs766004566	snp	C/T	3.33879e-05	0.00408568	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386466	GAAGTGGTGCCTGCT[C/T]AGCCCAGAGTCCCTA	57674
rs766005253	snp	C/T	5.01601e-05	0.00500775	synonymous-codon	RNF213	GRCh38.p7	17:80346648	CCTGGTGGGGAAGCC[C/T]GGCAGCTCCAAGTCT	57674
rs766008100	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80291886	AGGTGCCAATCCCGC[A/G]GTACTGGACGCGTCT	57674
rs766021274	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292620	CCATCTGTCAATAGA[C/T]GCGGGCGCTTCCCTT	57674
rs766028672	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265532	CCAAGAAATACAGTG[A/G]TGCTGGCTGGTTGCC	57674
rs766045517	snp	C/T	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358400	AGGCCAGATACTCCG[C/T]CCTGGGCAAGAGATC	57674
rs766051937	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395161	AAATTGTTTCATTTT[A/G]TGTGCTGTGCTTCAA	57674
rs766053171	snp	C/T	4.94173e-05	0.00497053	missense	RNF213	GRCh38.p7	17:80345204	GGGAAGAAGATCTAG[C/T]GCCCTTCTCCCTCCG	57674
rs766058007	snp	A/C	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389889	TCCTGTCTGCTCATA[A/C]GTCTGAACAGCTGCT	57674
rs766062875	snp	G/T	1.68886e-05	0.00290586	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363348	TGCCCTGAGCAAGCC[G/T]TGTGGTGCTTCCAAC	57674
rs766063689	snp	C/G			missense	RNF213	GRCh38.p7	17:80345715	AACTGCAGACATGAT[C/G]TACTCCAGAGTCAGG	57674
rs766070232	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371685	CAGCTGGTCTAAAAT[C/G]TGAGTTTTATATTCC	57674
rs766089693	snp	A/C/T	4.07434e-05	0.00451335	intron-variant	RNF213	GRCh38.p7	17:80343334	CTCCTCAGTAAGTGC[A/C/T]CTCCAGCGTCAGCCG	57674
rs766099236	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80294101	TCATTGACATCTTGG[A/G]TTTTCTAATTATTTT	57674
rs766100470	snp	A/G	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80319208	GAACCCCTCTCCCAG[A/G]TCACTGCCTACTGCA	57674
rs766110250	snp	G/T			missense	RNF213	GRCh38.p7	17:80345170	CCGGGGAAGCACATG[G/T]TCACCATGGATGGGG	57674
rs766114850	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80275636	GCCAGTCTACAGAGA[A/C]TGAGAGAGTATTATT	57674
rs766116492	snp	A/G	6.61638e-05	0.00575131	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353044	CAGCTGTTCGCGCCC[A/G]GAGACTTGCCTGAGC	57674
rs766135517	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80308987	TCTCCTAAATCCTTG[C/T]CGGGATTTCTCTTAA	57674
rs766148204	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80330266	TGCTTCCTCCAGGTT[-/C]CTTTCACTTGTTGAT	57674
rs766159397	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80333947	GGGGTTTGATCATCC[A/G]ATTCAGGGGTAAGAG	57674
rs766162624	snp	A/G	0.00019772	0.00994086	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379631	CTAGTGTGGCAGGCC[A/G]ATGGAACAGAGCATC	57674
rs766165427	snp	C/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80291735	ATAATGGGGAATCTT[C/T]TGAGTATGAGTTCAT	57674
rs766192207	snp	A/G	0.000228728	0.0106917	intron-variant	RNF213	GRCh38.p7	17:80278759	AGGGGGTCGTGTTTC[A/G]ACAGGGAGCTACATC	57674
rs766198096	snp	A/C	1.67618e-05	0.00289493	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383661	CAGAATTTTTTTTTT[A/C]ATTTTCTCCATCCAG	57674
rs766209580	snp	C/T	0.000160167	0.00894749	intron-variant	RNF213	GRCh38.p7	17:80336549	AATTCACCATCTTGT[C/T]ACCTAGAAAGCAGGA	57674
rs766226114	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80264303	GAGCTCTGCCTGGGT[G/T]AGTTTTTGAGGGGCC	57674
rs766228096	snp	G/T	1.64757e-05	0.00287012	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369598	GGACAACGCTCCGCC[G/T]GAGAAGGAAGTGATT	57674
rs766229035	in-del	-/GGCAGGCCGATG	1.64781e-05	0.00287033	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379623	TCTTCACCCTAGTGT[-/GGCAGGCCGATG]GAACAGAGCATCTGC	57674
rs766234594	snp	C/T	9.91785e-05	0.00704126	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379739	TCAGGATTCTATTTC[C/T]TAAGTACTCAAACTT	57674
rs766239398	snp	A/G	0.000197733	0.00994119	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393445	CTGCTCGCCAGCTGT[A/G]TCTCAGTGTGGAAAA	57674
rs766251434	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80318494	ACACAAGTGGAGAAC[A/G]CACAGACATGCCCCT	57674
rs766261004	snp	G/T	0.000116324	0.00762553	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393322	GGAGACTGTTTTAAA[G/T]GCTCTCTTCTTTGGT	57674
rs766269303	snp	C/T	6.84486e-05	0.00584975	synonymous-codon	RNF213	GRCh38.p7	17:80340061	CCTGCTGTTCGCAGA[C/T]CAGCTGAGCTACGAG	57674
rs766292366	snp	A/G	8.24192e-05	0.00641894	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364447	GAGCCCAGTGGAGTC[A/G]GATTTTCTCCACCGC	57674
rs766306845	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80290615	GTTCTTCCACGCCAT[C/T]ATCTCTCTTCATTTC	57674
rs766308565	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365394	CCCAAGGCTAAGGTA[C/T]CAGCTCCCCGGAGGC	57674
rs766317442	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357160	GACCTCAGGTGATCC[A/G]CCCGCCTCAGCCTCC	57674
rs766326168	in-del	-/TG	3.57929e-05	0.00423027	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374711	CCCATCACGTGACAC[-/TG]TATTGGAAGTCACGT	57674
rs766330841	snp	C/G/T	3.29632e-05	0.00405964	synonymous-codon, missense	RNF213	GRCh38.p7	17:80345773	AAGGACCAACATCAG[C/G/T]TGGACACCATCTTGT	57674
rs766339223	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80317667	GGAGCAAGCTCCGTG[C/T]AGGCCCTGCAGCAGT	57674
rs766349453	snp	A/G	8.25702e-05	0.00642482	intron-variant	RNF213	GRCh38.p7	17:80307248	CACATGCGGCCCCCG[A/G]GGGCTTCCTCTGACC	57674
rs766353906	in-del	-/CT			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393867	TGGCACTGCCCACCC[-/CT]CTTTTTTTTTTTCTT	57674
rs766365095	snp	C/T	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80344784	CCCTGAGGAGTGACA[C/T]AGAGCCTGGGATGGA	57674
rs766371968	snp	A/G	1.64857e-05	0.00287099	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361747	AGGACTGCCCAAGAA[A/G]TTCGTGGACATCTTT	57674
rs766373782	in-del	-/CCCCCCCAC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396727	CAGGAAAGTGCATTT[-/CCCCCCCAC]CCCCCCCCCCCAACC	57674
rs766377425	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80328073	TGCGTGTGCATTTTT[A/G]TAAAGGAGATAATCA	57674
rs766378943	snp	A/G	3.54509e-05	0.00421001	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389100	GCAGTGAAGGGGCTC[A/G]GCTCTCTTACCAGGT	57674
rs766387293	snp	C/T	1.65924e-05	0.00288027	intron-variant	RNF213	GRCh38.p7	17:80348326	CCTATCCCCTGTCAC[C/T]CAAGAGTCCTAAATC	57674
rs766396053	snp	C/T	3.34571e-05	0.00408992	synonymous-codon	RNF213	GRCh38.p7	17:80273395	CAAAGCCTCCTGGAC[C/T]GTCCAAGAAGTGAGT	57674
rs766402911	snp	A/T	1.6661e-05	0.00288621	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372647	CCTGCCAACGAGGCC[A/T]CGGTTGAATACCTGC	57674
rs766410541	snp	C/T	9.89968e-05	0.00703481	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354414	CAGCCACGGCCATGC[C/T]GAACGTCTGTTTCTG	57674
rs766417220	snp	A/G	4.94401e-05	0.00497168	missense	RNF213	GRCh38.p7	17:80346292	TTCAGGTGGTTCCAC[A/G]AGCACAGCGCGATGC	57674
rs766420025	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360737	GCCAGAAGATTTGCC[C/T]TAGTCCAGAAAAACC	57674
rs766421918	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80332908	TCCTCTTTTCATAAC[A/G]GGCATTTGTAAAGGG	57674
rs766429487	snp	C/T	1.65644e-05	0.00287783	missense	RNF213	GRCh38.p7	17:80340179	GACTGGGAGCACTGC[C/T]ACCTCCCCTCTGCCT	57674
rs766429880	snp	C/G	3.30077e-05	0.00406236	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388644	GTACAGACACGACTG[C/G]AACTATGAACATCTC	57674
rs766436929	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364580	GGCTGGCCTCAGCAC[A/G]TGCACGGATCCACCC	57674
rs766437352	snp	C/G	1.64825e-05	0.00287071	missense	RNF213	GRCh38.p7	17:80295801	TAAGCCACATCCTTG[C/G]GATACCTCAGAGGTA	57674
rs766449113	snp	C/G	1.69473e-05	0.0029109	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372715	TGCAGATTTCCTCTC[C/G]GAGCCTGAGGGAGGC	57674
rs766450002	snp	C/T	3.31846e-05	0.00407323	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381669	CGACGAGACCATCGG[C/T]GTGGTCCACCTCGTC	57674
rs766455432	snp	A/G	1.64743e-05	0.00287	intron-variant	RNF213	GRCh38.p7	17:80309011	CTCTTAACTCTTTGC[A/G]GGGCAGGATTCCCGA	57674
rs766463810	snp	A/G	6.59044e-05	0.00574002	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361817	GGAGAGCCGCAGCAG[A/G]AACTTCTTCAGTGTT	57674
rs766467391	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80338162	ACATTTGTAGGGTGC[A/C]TGGAACTCTAGTCCG	57674
rs766473060	snp	A/C/G	9.92103e-05	0.00704247	missense	RNF213	GRCh38.p7	17:80295686	CTGATTGTCCTTTTT[A/C/G]TAGTGGAAAAAATTG	57674
rs766473499	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310057	CACGCCCAGCCTCCC[A/G]TGGATCAGTTTTACC	57674
rs766473964	snp	A/T	1.64749e-05	0.00287005	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381565	CTGATAAACATCATT[A/T]AGCCTCCAGTGAGGG	57674
rs766481945	snp	A/G	0.41128	0.191021	intron-variant	RNF213	GRCh38.p7	17:80289609	AAAAAAAAAAAAAAA[A/G]AAAATGTGGAGGCCG	57674
rs766484791	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373384	CCGCGTTCCGCCTGC[C/G]CTTAGCATCCCCAGA	57674
rs766488195	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80285966	CAGGCCTGAGCCACC[A/G]CACCTGACCTATTGT	57674
rs766495696	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366670	GGATGGCTCAAAATA[-/A]AAAAAAAAAAATCTG	57674
rs766500100	snp	A/C/T	6.60126e-05	0.0057448	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375879	GCCAGAGGTGAGTAA[A/C/T]CGCCTGCAGGGCTGT	57674
rs766512506	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80306852	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	57674
rs766533490	snp	C/T	9.72432e-05	0.00697224	intron-variant	RNF213	GRCh38.p7	17:80331995	CTGACACTTTCTTTT[C/T]GCTTCTAAAGTGGAC	57674
rs766535736	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80350835	CGAGAGGTGTAAATA[A/G]TGGAACATTAACAAG	57674
rs766554320	snp	A/G	9.88321e-05	0.00702896	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390002	TTCATTTGCTCTTCC[A/G]TCGTTTTAGGAGCCA	57674
rs766559346	snp	A/G	1.66746e-05	0.00288739	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376554	TGGCGGTAAGAGTAG[A/G]CCACAATTCCATCGG	57674
rs766559888	snp	A/G	3.38816e-05	0.00411578	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385626	TGAGACGAACGGTTA[A/G]TATCCTGTCCCCTGT	57674
rs766567628	snp	C/G	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80345378	GAGACGTCATGACCA[C/G]GGACCTGTACCAGGG	57674
rs766578038	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296375	CAGCCTCTGTGTGCG[C/T]GTGTTTAGGAGGTTG	57674
rs766583527	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393841	AGTAATGACCTGTGC[C/T]CGTTCGCCTCTGGCA	57674
rs766589141	snp	C/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352315	TGAATCCTGGGATGG[C/G]AGGCTGCGTGCACCT	57674
rs766595659	snp	A/C	1.65209e-05	0.00287405	missense	RNF213	GRCh38.p7	17:80347967	TCCAGAAGAGGCACA[A/C]ATACAGCCCCTCTGA	57674
rs766605849	snp	C/G	1.70615e-05	0.00292069	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358524	GAGAAACTATCAGAA[C/G]ACAGCAGGACCCTAA	57674
rs766611133	snp	C/T	1.7098e-05	0.00292381	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385498	GGCCCTTTCAGGGGG[C/T]TGCTATCATACGGTT	57674
rs766624810	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325632	ATGTCCAAGCCAACA[C/T]TGATGACCTCAACAG	57674
rs766626384	snp	C/T	0.000114305	0.00755907	synonymous-codon	RNF213	GRCh38.p7	17:80337851	TCCCCAGACACGGTT[C/T]TGCACTTGATCCTTC	57674
rs766633912	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310148	CTCTGTCTGTGTGGT[A/G]CAGAGATCGGCAATT	57674
rs766636615	snp	A/G	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80306403	CGTTTTCCTGCTCAT[A/G]TCCTGGACTGTCTTT	57674
rs766655163	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80270415	GCTGGCACATTTACA[A/T]TGCAAATCTCTTCAA	57674
rs766657380	snp	C/T	1.64906e-05	0.00287142	synonymous-codon	RNF213	GRCh38.p7	17:80346363	CAGCAAAAATCACAC[C/T]GAGAGAGATCCCGTC	57674
rs766659905	snp	C/T	0.000117543	0.00766537	synonymous-codon	RNF213	GRCh38.p7	17:80332208	CTTCTGGCGGGAAGC[C/T]GCAGAGCCGCTGAGT	57674
rs766669666	snp	A/G	1.64933e-05	0.00287165	synonymous-codon	RNF213	GRCh38.p7	17:80290717	CAATATCTGTGAGCT[A/G]CACTACACCAGGTGA	57674
rs766673784	snp	C/T	1.7739e-05	0.00297812	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351678	TCTTTTTTTTTTCTT[C/T]AAATAGGTATTCTGT	57674
rs766679636	snp	A/G	1.68843e-05	0.00290549	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376897	CATGCTTTTCTTCCA[A/G]CCATGCCTGAAGACT	57674
rs766724424	snp	C/T	1.65018e-05	0.00287239	missense	RNF213	GRCh38.p7	17:80345510	CCGACCCCGACAAAA[C/T]GTATGAGCTCACAAC	57674
rs766766115	snp	A/G	4.94238e-05	0.00497086	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368031	CTGCCCTGCGACCAC[A/G]TGCACTGCCTGCGCT	57674
rs766767640	snp	A/T	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80306305	TGCTGAGCATAGACG[A/T]GCCTCTCTTCCGGTC	57674
rs766785127	snp	C/G	3.29533e-05	0.00405901	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390086	GCTCCTCAGCACATT[C/G]CTAAATCAGACTGGC	57674
rs766790699	snp	A/G	1.66106e-05	0.00288184	missense	RNF213	GRCh38.p7	17:80263778	GCAGCCCCCATAGCA[A/G]GTGAGGCCCAGGGGT	57674
rs766794633	snp	G/T	1.69886e-05	0.00291445	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288184	GACGCTTCCATCCCC[G/T]CTGGGGGCAGAGGCC	57674
rs766802999	snp	A/G	3.33734e-05	0.0040848	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363667	CAAGAAACACCCTGA[A/G]GCCCAGTCCCCAGGC	57674
rs766807394	in-del	-/T	1.70729e-05	0.00292167	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354194	CACCCCTCTTGCCCC[-/T]TGCCCCCACGTGGGC	57674
rs766813218	snp	A/G	0.000214135	0.0103451	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367803	TTGAGGCCGTGATGC[A/G]CACTCTCTGTGAATG	57674
rs766816544	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80348714	ACCAGGATGCGAGCT[C/G]AGATGAGATGTTCCC	57674
rs766829979	snp	C/T	0.000114266	0.00755778	synonymous-codon	RNF213	GRCh38.p7	17:80339320	GCAGGGTGTGTCCCT[C/T]CAAATGGACTTTGGC	57674
rs766830606	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359193	TTCCACTTCAGCTTT[A/C]AGGGGCTTCAATTCT	57674
rs766831703	snp	C/T	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80294909	TGAACAGCTTCTTCA[C/T]CCAGTTCGAGCAGTT	57674
rs766835043	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369134	CCAGGCATGGTGGCT[C/T]ACGCCTGTAATCCCA	57674
rs766855367	snp	A/G	1.67365e-05	0.00289275	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363620	CCAGACCCTGGACGC[A/G]TTTGCCGCAATGGCC	57674
rs766874565	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272670	GGTGGGGATGGACAA[A/G]GTGCGTCCACACCAC	57674
rs766905174	snp	A/C/T	3.92837e-05	0.00443177	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373189	CGGGGCCGGGCAGCA[A/C/T]ACAAACATGCACCCC	57674
rs766907090	snp	A/T	5.96837e-05	0.00546244	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353507	CACGTTTGCTTCGAC[A/T]GCAGTGGGCTTGGAA	57674
rs766920611	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358777	AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTATTCC	57674
rs766949969	snp	A/G	1.65356e-05	0.00287533	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360060	CCTCACCTTATTGCA[A/G]ACATAAAGGTGAGAT	57674
rs766958418	snp	C/T	4.98575e-05	0.00499262	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376542	CCCCAGCCACCATGG[C/T]GGTAAGAGTAGGCCA	57674
rs766961994	snp	A/G	1.70831e-05	0.00292254	intron-variant	RNF213	GRCh38.p7	17:80306475	AATACGCAGGTTTGT[A/G]TCTGAAGTCGGCTCT	57674
rs766967349	in-del	-/GTATTTTTCTCAGAAACTATGTAAAAAACCCAAAAC	5.24251e-05	0.00511955	intron-variant	RNF213	GRCh38.p7	17:80350408	CTAAGTATGTTTTTA[lengthTooLong]GTAGGAAGTCCTAGA	57674
rs766969385	snp	A/G	4.94295e-05	0.00497115	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358423	AAGAGATCTTTGGAT[A/G]TTTATTTTCAGTGAC	57674
rs766969469	in-del	-/CT	1.65176e-05	0.00287376	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361724	CCGCTCCTTGGTTTC[-/CT]CTCTGCAGGACTGCC	57674
rs766973852	in-del	-/AT			intron-variant	RNF213	GRCh38.p7	17:80281188	ACCCTCCACACACAC[-/AT]ACCCCACTCACACCA	57674
rs766977927	snp	A/G	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345972	CTGGTTTGGGCTACA[A/G]GGTTAGTATGGAGGA	57674
rs766980050	snp	C/T	1.68482e-05	0.00290238	missense	RNF213	GRCh38.p7	17:80347006	AACTGGGCCCTTGAC[C/T]CTGCCAAGATGAACC	57674
rs766983996	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80262768	CCCACCCAGTGCCTC[C/T]GTCCCTCGTTCAGGC	57674
rs766990937	snp	C/T	1.64917e-05	0.00287151	missense	RNF213	GRCh38.p7	17:80347828	CACTTTCCCATCCCC[C/T]TCATTAACCGGCTGG	57674
rs766992553	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80265154	CGGGTTCAAGTGATT[C/G]TTCTGCCTCAGCCTC	57674
rs766998094	snp	A/C	1.66949e-05	0.00288915	missense	RNF213	GRCh38.p7	17:80346920	TGAAGACTCTGCACC[A/C]GCTGCTGGAAGACGG	57674
rs767001783	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80306270	TTCCCTACTTCAGTT[C/T]ATGAGAGAGAAGCAG	57674
rs767005368	snp	A/G			missense	RNF213	GRCh38.p7	17:80346364	AGCAAAAATCACACC[A/G]AGAGAGATCCCGTCC	57674
rs767022210	snp	A/G	4.94923e-05	0.0049743	missense	RNF213	GRCh38.p7	17:80313157	CATTCACATACGTCA[A/G]GGAAATTGAGGTAGG	57674
rs767047925	snp	A/G	1.66729e-05	0.00288724	intron-variant	RNF213	GRCh38.p7	17:80291843	GTAAGTCGTGGCAGC[A/G]GGCTGTCTGCTCACC	57674
rs767059655	snp	A/C/T	3.32653e-05	0.0040782	intron-variant	RNF213	GRCh38.p7	17:80273199	CCTTCCTAACACTCG[A/C/T]TTCTCTCTGAGATCT	57674
rs767065206	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388314	GTGGCTGAATGAATA[A/T]ATGAATGGGATATGC	57674
rs767083151	snp	A/G	1.66076e-05	0.00288158	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383675	TCATTTTCTCCATCC[A/G]GCATCTAGATAAAAC	57674
rs767085311	in-del	-/TTAATG	0.000131795	0.00811665	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376275	ATTCTTTGATACATC[-/TTAATG]TTAAGTTTTTTTCCT	57674
rs767105240	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378568	CTCAAGCGATCCTCC[C/T]GCCTCGGCCTCCCAA	57674
rs767106950	snp	C/T	1.67217e-05	0.00289147	synonymous-codon	RNF213	GRCh38.p7	17:80346663	CGGCAGCTCCAAGTC[C/T]CTCGCCAAGACCATC	57674
rs767111568	snp	C/T	1.66369e-05	0.00288412	missense	RNF213	GRCh38.p7	17:80346767	CCTTCCAGTGCAGCC[C/T]GCACTCCACCCCACA	57674
rs767113425	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352575	TACTTGAATAATTTC[A/G]TGGAGAATGGAAGGC	57674
rs767114173	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379661	CTGCATTGACTGCCA[C/T]GCGCCGATTGGAGGC	57674
rs767122649	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80294561	GTTGGAGGAGTCTGG[C/T]TGTCGTCAGTGTGTG	57674
rs767124019	snp	A/G	1.64762e-05	0.00287016	missense	RNF213	GRCh38.p7	17:80294742	TCAGTACTATGACAT[A/G]GTTTATATGAAGCCT	57674
rs767143436	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80316945	TCAGAATAAAAAGCC[A/G]GTTGTGCAGTAGGAG	57674
rs767151028	snp	G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397940	CAGGCAATTGCCCCA[G/T]TGGAATGCCTGGCCA	57674
rs767166380	snp	C/T	1.64787e-05	0.00287038	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393461	TCTCAGTGTGGAAAA[C/T]AGCTGCTGTGCTGAA	57674
rs767168847	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361451	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	57674
rs767175571	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80297058	GCAAAGGCAATGTAC[A/G]GAGTTAGTGCCGGGG	57674
rs767202360	snp	A/C	1.67304e-05	0.00289222	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358500	TGGAAGGCTTTCTTT[A/C]CCTGGGGAGAGAAAC	57674
rs767205642	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80335219	ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCCCACA	57674
rs767230962	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80299089	GTCCAAATATGGATT[C/T]GTGGGTGTTTTATGT	57674
rs767232796	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80275323	TCCCTTTTTATGCCT[A/G]ATTTGGAACTCTGTC	57674
rs767258152	snp	A/T			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259535	CAGGTTTTGTGTGTT[A/T]GTTAGTTTTTGAGGC	57674
rs767282673	snp	A/G	1.6599e-05	0.00288084	intron-variant	RNF213	GRCh38.p7	17:80348332	CCCTGTCACCCAAGA[A/G]TCCTAAATCCCTCGT	57674
rs767283195	snp	C/T	1.65578e-05	0.00287726	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393544	TTGGAGAGAAGACTC[C/T]TCTCTCCTCGTCTGC	57674
rs767285154	snp	A/G	4.94613e-05	0.00497275	missense	RNF213	GRCh38.p7	17:80289683	ACCAAGACCAAGGAC[A/G]AGATGGCTGCTGCTG	57674
rs767292938	in-del	-/CT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384603	TGTCAATACTGTGGC[-/CT]CTCTCTCAGATGCAG	57674
rs767297264	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361837	TCTTCAGTGTTACTT[A/G]AAGGATTTCATTCTC	57674
rs767307402	in-del	-/TGTCTT	3.30284e-05	0.00406363	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380804	GCCAGCCTCAGCCTC[-/TGTCTT]GTGTTCTCTCGTTCT	57674
rs767314590	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307276	ACCCCTATAATTGGC[C/T]GTGACCCACATGTGC	57674
rs767321343	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80325371	TCAGAGTGTCTTGCG[C/T]TGTAAATAATAACTA	57674
rs767321816	snp	G/T	1.65515e-05	0.00287671	missense	RNF213	GRCh38.p7	17:80340212	AGCCAGCACAAGGTC[G/T]TCGTCACCCCCCAGG	57674
rs767333545	snp	C/T	3.29745e-05	0.00406031	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369697	TTCTTCCTGTAAACC[C/T]AGCCCCTCATTTCTT	57674
rs767337241	snp	A/G	3.29516e-05	0.00405891	missense	RNF213	GRCh38.p7	17:80345932	CGGAAGCACTCTGAG[A/G]AGATGATCTGCCGTT	57674
rs767338759	in-del	-/T	1.65652e-05	0.0028779	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384990	GTAACCCCAATAACA[-/T]TTTTTTAGGTAAATA	57674
rs767340250	snp	C/T	3.29478e-05	0.00405867	synonymous-codon	RNF213	GRCh38.p7	17:80309024	GCGGGGCAGGATTCC[C/T]GAGGAGGCCTTGTCA	57674
rs767340671	snp	A/G	4.95356e-05	0.00497648	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354562	GGACGCTCTCCAGGA[A/G]GCGGGCACATTCAGG	57674
rs767360172	snp	A/G	0.000114123	0.00755303	intron-variant, missense	RNF213	GRCh38.p7	17:80278806	GCTGCTGTAGACCTC[A/G]TATCCGATGAATGGG	57674
rs767367885	snp	C/T	0.000115311	0.00759224	synonymous-codon	RNF213	GRCh38.p7	17:80344905	TCAAGAAGGCTCTGT[C/T]GAAGGCACCCCGGAG	57674
rs767371073	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389229	GCTGCAGTCCTACAG[C/T]GATGCCTGTGAAGTG	57674
rs767376348	snp	G/T	1.64885e-05	0.00287123	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364513	GCCGCGTCCCCGAGT[G/T]ACAGGGGCTGGTGAC	57674
rs767384250	snp	G/T	1.64746e-05	0.00287002	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376282	GATACATCTTAATGT[G/T]AAGTTTTTTTCCTGT	57674
rs767393102	snp	C/T	1.65847e-05	0.0028796	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379754	CTAAGTACTCAAACT[C/T]TGGGGTGTTGGGCTG	57674
rs767401472	snp	A/G	0.00147526	0.0271193	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389114	CGGCTCTCTTACCAG[A/G]TGGTGAGATGCCAGA	57674
rs767404535	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80305589	GTATTCTGAATTCTA[C/T]ATTAAGTTAATTCTC	57674
rs767413935	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379790	ATTCCAGCTGATAAA[G/T]TGATACTCAAGATAG	57674
rs767418198	in-del	-/AGA	1.8442e-05	0.00303656	cds-indel	RNF213	GRCh38.p7	17:80289789	CTGCTGTGAAAAACG[-/AGA]AGGAGCAAAAAAACC	57674
rs767419604	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391617	TTTGCATAGAACAGG[C/G]GTTCATCTTCTCTGC	57674
rs767455876	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266883	AAAGCTGAGATAGGC[C/T]GATAGCTAGGCCTCT	57674
rs767472849	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80265715	GCACCAGCTCTCACG[C/T]GATTAGCTGAGTTAA	57674
rs767473789	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357396	ATCCACCCATCTGTC[C/T]GTCCGCCCATCTATC	57674
rs767494230	snp	C/T	1.65474e-05	0.00287636	intron-variant	RNF213	GRCh38.p7	17:80295817	GATACCTCAGAGGTA[C/T]TATTATTTTTTGTCA	57674
rs767514563	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390016	CGTCGTTTTAGGAGC[C/T]ATTTGGGGAAATCAG	57674
rs767516820	snp	A/G	8.24056e-05	0.00641841	synonymous-codon, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351769	AAAACTGTCCCGGGT[A/G]GGAAGAGGAACAGCC	57674
rs767517394	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334862	CGATCTCCTGACCTC[A/G]TGATCAGCCCGTCTT	57674
rs767526763	snp	C/G	3.32143e-05	0.00407505	missense	RNF213	GRCh38.p7	17:80298343	CTGTACCTGGTGAAC[C/G]TGTGCCAAAGATGCA	57674
rs767529938	in-del	-/AC			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320709	ATAATGTTTTGAAAG[-/AC]CGCTCAGGCTGGACA	57674
rs767534654	snp	C/T	1.64852e-05	0.00287094	missense	RNF213	GRCh38.p7	17:80345411	TGCTGCTCCAGAGGG[C/T]GCCCTTCAATGTCGA	57674
rs767542075	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80277172	CAGATACAAGAGGCC[A/C]TGTATGATTCCTTTG	57674
rs767552247	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382433	TCCTGCCCCATGACA[A/G]GAAAATCTGCTCCCA	57674
rs767552381	snp	A/G	6.59707e-05	0.00574291	missense	RNF213	GRCh38.p7	17:80346376	ACCGAGAGAGATCCC[A/G]TCCTCTGGTCGTTGA	57674
rs767563845	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356331	AATCCCTGACTCCAC[A/T]CCCCGGGACCAGCCC	57674
rs767581628	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328231	ATCCTAGTCCTTCTC[C/T]TGGTGGCGGGGAAGG	57674
rs767602309	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80297904	CGAGGTTATAATGAT[C/T]GCACCACCGCGCTGC	57674
rs767605762	snp	A/G	0.000130813	0.00808637	missense	RNF213	GRCh38.p7	17:80332576	TCATCTTGCAGGTCA[A/G]AGAGAGCCTGGGACT	57674
rs767612755	snp	C/T	2.13819e-05	0.00326963	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372961	ACTCACCCGCTTTCT[C/T]GTTGGCCTCTCAGAG	57674
rs767631735	snp	C/T	1.70769e-05	0.00292202	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287803	AAAGTGAGTGTCTCT[C/T]TTTCTGTTTAGAGCA	57674
rs767634608	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328887	ATCACAAGTGAACCA[C/T]GAAAGAAACCGTCAT	57674
rs767635828	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80276081	TTTATTTATTTATTT[A/G]TTTATTTTTTGTTTT	57674
rs767653665	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365558	AGAGCCCAATCCCGG[A/G]CACGCACACGCCACA	57674
rs767675573	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378013	TGGACGTGGCTCTGC[A/G]GCGTGGGCTGTCCTG	57674
rs767680585	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80327612	AGGAAGTTGTTCAGG[G/T]GATGAATCTGGGCAA	57674
rs767686409	snp	C/T	1.65836e-05	0.0028795	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390159	AAACTAAAGAACCCC[C/T]AAACCCAAACCGAGG	57674
rs767687852	snp	A/G	4.96726e-05	0.00498335	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386290	CTGCAGCACTGACTT[A/G]GATCTGGACACTGAG	57674
rs767722896	snp	A/C/G	9.98094e-05	0.00706369	synonymous-codon	RNF213	GRCh38.p7	17:80273272	CTCCACAATGGCGTC[A/C/G]GCCTCGGAGGGTGAA	57674
rs767733457	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329790	GAGCCGAAATCACGC[C/T]ACAACACTCCAGCTT	57674
rs767739763	snp	A/G	3.29598e-05	0.00405941	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390095	CACATTCCTAAATCA[A/G]ACTGGCCTAGACGCC	57674
rs767739924	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364814	GCAGAAAGGGGCTGA[C/T]GCAGGGAACATGCTT	57674
rs767744963	snp	A/G	4.98965e-05	0.00499457	intron-variant	RNF213	GRCh38.p7	17:80273215	TTCTCTCTGAGATCT[A/G]ACCCTTCCTTCATCT	57674
rs767748024	snp	A/G	3.30633e-05	0.00406578	missense	RNF213	GRCh38.p7	17:80347984	TACAGCCCCTCTGAC[A/G]TCTTCATCGGCTACC	57674
rs767748357	snp	A/G	3.30529e-05	0.00406514	missense	RNF213	GRCh38.p7	17:80346454	TCATATCGGAAAGCC[A/G]TCGCCAGGTTCTTTC	57674
rs767758584	snp	A/G	3.36457e-05	0.00410143	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381689	TCCACCTCGTCCTGC[A/G]CAGGCTTCTCCAAGA	57674
rs767763506	snp	C/T	6.79787e-05	0.00582964	intron-variant	RNF213	GRCh38.p7	17:80295026	GCTTGCCACCAGCTG[C/T]TCTACCTGCTGGGCA	57674
rs767782203	snp	A/G	3.41799e-05	0.00413385	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363751	ATGAGCACATGCAAG[A/G]CAGCGGGAGCCTGGC	57674
rs767791421	snp	A/G			missense	RNF213	GRCh38.p7	17:80339823	GGTCTCCCGTGGAGC[A/G]TTGTCTCCCGAGAGG	57674
rs767798502	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269248	CTCTGACAACACCCT[C/T]ACAGACACAACCAGA	57674
rs767801568	snp	C/T	3.2956e-05	0.00405918	missense	RNF213	GRCh38.p7	17:80306419	TCCTGGACTGTCTTT[C/T]AGGGATTTACTACCG	57674
rs767815994	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286097	GTCTCCTCTGTCCAC[A/G]CCCAAACGCACCAAG	57674
rs767822827	snp	C/T	1.67287e-05	0.00289207	missense	RNF213	GRCh38.p7	17:80347028	AGATGAACCGGGGCA[C/T]TTTTGTGTCACGTGG	57674
rs767830043	snp	A/G/T	3.32907e-05	0.00407976	intron-variant	RNF213	GRCh38.p7	17:80344048	TTTTCGCCTGGCGTG[A/G/T]GGGGCTCTTGGGTTC	57674
rs767835468	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296477	CCCTGCCTGTGCCGT[A/G]TCTAGTTCAGGAAAC	57674
rs767836366	snp	A/G	3.31719e-05	0.00407245	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371935	AAAAAGAAAGCATTC[A/G]TAACTGAAGATAAAA	57674
rs767836725	in-del	-/CCAGGACGCTCT	3.29755e-05	0.00406038	cds-indel, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354544	AAGGGAAGCCTGCAA[-/CCAGGACGCTCT]CCAGGAGGCGGGCAC	57674
rs767846460	snp	G/T	0.000114528	0.00756643	missense	RNF213	GRCh38.p7	17:80339691	CAGAGTTCAGCCTGG[G/T]GGACAAGCTGAGGAT	57674
rs767851415	snp	A/C/T	6.69718e-05	0.00578637	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363682	AGCCCAGTCCCCAGG[A/C/T]GTGGCTACAGTTGGT	57674
rs767852983	in-del	-/AAG	3.33356e-05	0.00408248	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363653	CACGGAGATGCTGAC[-/AAG]AAACACCCTGAAGCC	57674
rs767882653	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279813	GAGTATTACAGGACT[C/T]ACTAATAATATCAAA	57674
rs767888229	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375978	TAATTTTTTTATCTA[C/G]GATAGAGGTTCTCAA	57674
rs767888743	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80350855	CATTAACAAGCTATA[-/T]AAAGGATGCCTTTGA	57674
rs767888855	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80281981	CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA	57674
rs767890698	snp	C/T	3.56424e-05	0.00422136	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374708	CAGCCCATCACGTGA[C/T]ACTGTATTGGAAGTC	57674
rs767913474	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359361	TGAGACCCCATCACT[A/G]CAAAAAATTTAAAAA	57674
rs767930136	snp	C/G	2.15673e-05	0.00328378	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386884	GCAAGCCCCGGCTGA[C/G]CCTCAAGGTAGGGCT	57674
rs767934573	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80305547	ATAGGAGCATGCCCA[G/T]AATGGCCAGCAGTGA	57674
rs767938713	in-del	-/TCTA			intron-variant	RNF213	GRCh38.p7	17:80269476	CATCCATTCATCTAT[-/TCTA]TCTATCCATCCATCC	57674
rs767949875	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80280566	TCAAGCAATCCTCGT[A/G]CCTCAGCCTCCCGAG	57674
rs767951058	snp	A/G	3.74237e-05	0.00432556	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360186	TGTGGGTCCAGGCTC[A/G]GTACATCACAGACGC	57674
rs767955326	snp	A/G	1.6477e-05	0.00287024	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353696	TTGGGACCTCCCCTT[A/G]TGCTGCTGGTGATGC	57674
rs767963102	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80322004	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC	57674
rs767973550	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80350127	ACCATCCTCGGACCT[C/T]GTTAGGAGGCATTCC	57674
rs767976567	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385389	CTAGCTCCTCAAACT[C/T]GGCTCACTCCTTCAA	57674
rs768001580	in-del	-/A	1.68488e-05	0.00290243	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358512	TTTCCCTGGGGAGAG[-/A]AACTATCAGAACACA	57674
rs768002366	snp	A/G	5.21517e-05	0.00510619	intron-variant	RNF213	GRCh38.p7	17:80306485	TTTGTGTCTGAAGTC[A/G]GCTCTGGAGTCCTGG	57674
rs768003239	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80269771	ATCCATCCGTCCATC[C/G]ATCCATGTATCTACC	57674
rs768010427	snp	C/T	1.6531e-05	0.00287493	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360080	AAAGGTGAGATGGCC[C/T]ACATCGTGGTGCAGA	57674
rs768013302	snp	C/G	1.64735e-05	0.00286993	synonymous-codon	RNF213	GRCh38.p7	17:80346168	CCTAGATGAAAACGG[C/G]ACTCGCGTGATCACA	57674
rs768023486	snp	C/T	1.64844e-05	0.00287087	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380930	CCCAGTGGTCTTCCT[C/T]CTTATCCGGCTACTC	57674
rs768045200	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389058	AGTGTCAGCTGTTAG[A/G]GAGTTGGCCCCCCGC	57674
rs768059821	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393564	TCCTCGTCTGCGGCG[C/T]GGACTTGATCATGGA	57674
rs768064041	snp	A/C/G	8.36343e-05	0.00646614	intron-variant	RNF213	GRCh38.p7	17:80349956	TCCCCAGCCGCAGCC[A/C/G]TGTGGCTTCTGCGTG	57674
rs768064776	snp	A/G	1.66632e-05	0.0028864	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363650	CTGCACGGAGATGCT[A/G]ACAAGAAACACCCTG	57674
rs768070283	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370255	TAGATGTCTCCTAAG[C/T]TTCTATTCCCCTGAA	57674
rs768076521	snp	C/G	6.62603e-05	0.0057555	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385016	AAATAAAAATTGTTA[C/G]TGGGTGGTCTTCCCT	57674
rs768083947	snp	A/T	6.58913e-05	0.00573945	missense	RNF213	GRCh38.p7	17:80345143	CCATCACTCCACACC[A/T]CTGACCAAAGCCCGG	57674
rs768093727	snp	G/T	0.000149747	0.00865164	missense	RNF213	GRCh38.p7	17:80306458	GACTTGAGCAAGTCT[G/T]GAATACGCAGGTTTG	57674
rs768103241	snp	C/T	4.99297e-05	0.00499623	missense	RNF213	GRCh38.p7	17:80347133	TCCAAGGGTACTTTG[C/T]GTCCTTTGCCAAAGC	57674
rs768110157	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290273	TGTGCATTACGAACA[C/T]AAGGACCATGTGCCT	57674
rs768111487	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80307120	TTTTCTTTTTTTCTC[-/T]GCCTTAGGATGTTCA	57674
rs768111978	snp	A/G	4.94197e-05	0.00497066	missense	RNF213	GRCh38.p7	17:80343957	ACCCCTGCCATTTGT[A/G]TATCGTTGAAATCCT	57674
rs768123699	snp	A/G	4.27542e-05	0.00462334	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372490	GTTTAAAAAAATAAT[A/G]TCCTTTTCTTTCTTG	57674
rs768132103	snp	A/C	1.68071e-05	0.00289884	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388561	TTGTCATCTGCTGGA[A/C]ATGTCCACGATGGAT	57674
rs768134977	snp	C/T	1.65097e-05	0.00287308	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374553	GGCCAAAGCTGTCCT[C/T]GAGTGCAAGCCACTG	57674
rs768136579	snp	A/C	3.29451e-05	0.00405851	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377726	GGTCATTGGGTGAAA[A/C]CTCATTAGCCAATGT	57674
rs768142611	snp	A/G	0.000114175	0.00755476	missense	RNF213	GRCh38.p7	17:80327878	CTGATAGCTGTTGCC[A/G]ACTCTGTGTTGACGA	57674
rs768166426	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390474	CAACCTTGGCTCACT[A/G]CAACCTCTGCCTCCC	57674
rs768172702	snp	A/G	3.3911e-05	0.00411756	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363735	GAGCTCATCTGCTCC[A/G]ATGAGCACATGCAAG	57674
rs768174923	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296947	ACCTCCCAAAGTGCT[A/G]GGATTATAGACATGA	57674
rs768187659	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80273462	GCCCAGGAAAATCTC[A/C]CTGCACAGCTGCCCA	57674
rs768187944	snp	A/G	3.46614e-05	0.00416287	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376963	CGAGTCCACTGGTAC[A/G]GTAAGTGTTGGGGTC	57674
rs768198475	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290468	GAGTGCATGTGTGTG[C/T]GCACGTGTGTGTGCG	57674
rs768213323	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328554	AAGAATGGATCACAG[C/T]AGCAGATCTTTATTT	57674
rs768216512	snp	A/G	3.29533e-05	0.00405901	missense	RNF213	GRCh38.p7	17:80345567	TCGAGATGCGGTTCC[A/G]GTGTGGGATCCCGGT	57674
rs768224078	snp	A/G/T	3.29458e-05	0.00405857	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376382	TTTGCAACATCGCTC[A/G/T]TGGACAATTCTGTGC	57674
rs768231163	snp	C/G	1.66579e-05	0.00288595	intron-variant	RNF213	GRCh38.p7	17:80273195	TTTTCCTTCCTAACA[C/G]TCGCTTCTCTCTGAG	57674
rs768246279	in-del	CATCCATCCATCCATTCATCTATTCTATCTATCCATCCATCTATTCATCCATCCATTCATCTATTCTATCTA/TT			intron-variant	RNF213	GRCh38.p7	17:80269412	GTCCTATCATCTATC[lengthTooLong]TCCATCCATCCATTC	57674
rs768258155	snp	A/G	1.65078e-05	0.00287291	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390129	CTGCTAGAGCTGCAC[A/G]AAATGATAATCTTGA	57674
rs768260231	in-del	-/CATT			intron-variant	RNF213	GRCh38.p7	17:80269673	ATCTATCCATCCATC[-/CATT]CATCTGTTCTATCTA	57674
rs768274164	snp	A/G	1.85479e-05	0.00304526	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386867	CAGCCGCTTCCTCCA[A/G]GGCAAGCCCCGGCTG	57674
rs768285763	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369927	TCTCTTCATCGCAGC[A/G]TTTTGTTACCAAGTC	57674
rs768294637	snp	A/C	1.65102e-05	0.00287312	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369474	TGGGAAACACCATCC[A/C]CCTGTCTTCTGTTTC	57674
rs768295348	snp	A/T	6.59131e-05	0.0057404	missense	RNF213	GRCh38.p7	17:80346059	CTCTGCCCCCGAGCC[A/T]GATTCCTCTGGTGTG	57674
rs768296294	snp	A/G/T	3.35409e-05	0.00409506	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354021	TCTCCACCAACAGGT[A/G/T]TCGATCCTGGACACC	57674
rs768297572	snp	A/G	1.6501e-05	0.00287232	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367755	TTCTTCAGTGTCTTC[A/G]AGAGAACTCTGACGT	57674
rs768321928	in-del	-/C	1.64741e-05	0.00286998	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368018	GACCCCGTCTGTCTG[-/C]CCCTGCGACCACGTG	57674
rs768325992	snp	C/T	7.37232e-05	0.00607093	synonymous-codon	RNF213	GRCh38.p7	17:80289787	AGCTGCTGTGAAAAA[C/T]GAGAAGGAGCAAAAA	57674
rs768337644	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351809	TTCCACGGAGGTGAG[A/G]TCAGAACATCAGTCA	57674
rs768338465	snp	G/T	0.000122858	0.00783669	missense	RNF213	GRCh38.p7	17:80339862	TCGGCCAGCCCAACC[G/T]CGTCGTCTGTGGCCA	57674
rs768341680	snp	C/T	6.61802e-05	0.00575202	synonymous-codon	RNF213	GRCh38.p7	17:80348013	CCACTCGGACGCCTG[C/T]GCGTCTGTGGTGCTG	57674
rs768361501	snp	C/T	3.30568e-05	0.00406538	synonymous-codon	RNF213	GRCh38.p7	17:80294983	CAGCTGTGGACCGAT[C/T]TGCAGTACAGGGAGA	57674
rs768365997	snp	C/T	1.6574e-05	0.00287867	synonymous-codon	RNF213	GRCh38.p7	17:80347104	CTCCTCAGACATCCT[C/T]GTCCAGGACCGAGTC	57674
rs768366030	snp	C/T	1.65688e-05	0.00287821	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383977	TCGGTGCAGAGTTCC[C/T]CAGCAGGCCTGAAGG	57674
rs768367050	snp	A/G	1.64806e-05	0.00287054	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380905	TGGTGACATGTGACC[A/G]AGGGCTGCCCCCAGT	57674
rs768367524	snp	G/T	2.63612e-05	0.00363042	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374649	TTGGAGCCTGCATGT[G/T]CCCTGGTTTATGTCA	57674
rs768384262	snp	C/T	0.000284279	0.0119188	intron-variant	RNF213	GRCh38.p7	17:80349937	TTCCCTGCTGCCCTC[C/T]CCCTCCCCAGCCGCA	57674
rs768387039	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80301022	TTTGTGTATGTTCCT[A/T]ATAGATGCTGGATAT	57674
rs768396148	snp	C/T	4.05556e-05	0.00450291	intron-variant	RNF213	GRCh38.p7	17:80289884	ACCCTGCCTGAGAGC[C/T]CGGCACACCCTCTCC	57674
rs768401853	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	RNF213	GRCh38.p7	17:80346147	GAGACTGGTTGAGTC[C/T]ATCAGCCTAGATGAA	57674
rs768419878	snp	A/G	1.64806e-05	0.00287054	intron-variant	RNF213	GRCh38.p7	17:80307121	TTTCTTTTTTTCTCT[A/G]CCTTAGGATGTTCAG	57674
rs768422002	snp	A/C	1.88074e-05	0.00306649	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371887	AGCTTTCATGATGTA[A/C]AAGATTATATTCAGG	57674
rs768425732	snp	A/C/T	4.98926e-05	0.00499442	missense	RNF213	GRCh38.p7	17:80273259	CTGAGAACAATAACT[A/C/T]CACAATGGCGTCGGC	57674
rs768429331	snp	C/T	1.65206e-05	0.00287403	synonymous-codon	RNF213	GRCh38.p7	17:80348088	TCACCAGAAGGTGTC[C/T]GAGGAGGCCAAATCG	57674
rs768436713	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80308539	TCCCTACCGAGTCCC[A/T]CCTAAGGCTCCTCCT	57674
rs768439060	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337324	AGATGTAAGTCAAGT[A/G]CCCCCATGTGCCAGC	57674
rs768452142	snp	C/T	5.07009e-05	0.00503467	synonymous-codon	RNF213	GRCh38.p7	17:80346978	CAAAAAGGTCGGCTT[C/T]GTGGGCATCTCCAAC	57674
rs768455331	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80339191	CAACCTCATGGTTCT[A/G]CCTCTCCAGGTCTTC	57674
rs768473191	snp	C/G/T	3.30574e-05	0.00406544	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380983	GAGCGTCCCAGAGTT[C/G/T]CCAGGTATAACCCAG	57674
rs768475126	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375150	AGTTTCTAAGACCAG[G/T]GAAGGAGTCAGAAGA	57674
rs768515955	in-del	-/CCCCCCCAC			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396726	CAGGAAAGTGCATTT[-/CCCCCCCAC]CCCCCCCACCCCCCC	57674
rs768522941	in-del	-/AAAG	1.64906e-05	0.00287142	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393379	AGTTACATGCAAACT[-/AAAG]AAAGTGAAATTCTTC	57674
rs768527490	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80349207	CAGCAGGTTGTGGGA[G/T]GCTAGTGATGATGTC	57674
rs768536023	snp	A/G	4.957e-05	0.00497821	missense	RNF213	GRCh38.p7	17:80343209	GTGCCTCTGAAAACA[A/G]TTCGACTGATCGACC	57674
rs768549249	snp	A/G	1.64754e-05	0.00287009	intron-variant	RNF213	GRCh38.p7	17:80306231	GCGTCTCTTTTCTCC[A/G]TCCCTATTTCTCTTA	57674
rs768553972	snp	C/T	0.000144749	0.0085061	intron-variant	RNF213	GRCh38.p7	17:80325231	CTGGGAACATCAGCT[C/T]AGGCAAGGTGGTGTC	57674
rs768555073	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290354	GTGTGTGCGTGTGCA[C/T]GTATGTGTGCGTGTG	57674
rs768557653	snp	A/G	1.64898e-05	0.00287135	intron-variant	RNF213	GRCh38.p7	17:80309210	TATCACACCCGGGAT[A/G]GGTGCGGAATTTCAA	57674
rs768560978	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384834	GGCTCCCTCTTCGCC[A/G]CCCTCCATTTCTAGC	57674
rs768572081	snp	C/T	8.32688e-05	0.00645194	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319527	TCCCTGCTGCTCGCA[C/T]CATCCTGCATGTGTT	57674
rs768573569	snp	A/G	1.71105e-05	0.00292489	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373151	GTGTTTCCCAAGGAC[A/G]TTGTCAAGCAGCAGG	57674
rs768584122	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368537	TCCTGGGTTCAGGCA[A/G]TTCTCCTGCCTCAGC	57674
rs768591599	snp	C/T	1.64817e-05	0.00287064	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386370	CTCTCGTCAGCTACT[C/T]GATTCGCCTACACAA	57674
rs768604506	snp	C/T	1.68972e-05	0.0029066	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383635	ATCTGTTTGTAGCAA[C/T]ACCTCACTTCCAGAA	57674
rs768615464	snp	A/C	1.67058e-05	0.00289009	missense	RNF213	GRCh38.p7	17:80350314	AGAAACTGTTTAACG[A/C]ATACAGCCAAATGTA	57674
rs768624860	snp	C/T	1.65116e-05	0.00287324	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376507	TGAACTCTTGGAGCC[C/T]CTAAAGAATCTGGCC	57674
rs768657248	snp	A/G	1.6534e-05	0.00287519	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386431	CAAGGAAAACAACAG[A/G]TTTGTGCACGAGCCA	57674
rs768669207	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80342240	TCGGCTCTACCATCT[G/T]GGTTTCTGCAGGCAC	57674
rs768677550	snp	A/G	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367805	GAGGCCGTGATGCGC[A/G]CTCTCTGTGAATGCA	57674
rs768697961	snp	C/T	8.23608e-05	0.00641667	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376410	TGCCATTGTTGAGGG[C/T]GGGGCCTAGTGACAG	57674
rs768701085	snp	C/G	1.67424e-05	0.00289326	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363326	GATGGTATGGCCCTC[C/G]TCCGCCTGCCCTGAG	57674
rs768715519	snp	A/C	9.70827e-05	0.00696648	intron-variant	RNF213	GRCh38.p7	17:80336466	GTGGAAATGGTGGCA[A/C]ACCTGTGTGGTAGGT	57674
rs768724213	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319056	ACATGCTTTGCGTGG[A/G]CCAGGAGAAGCTTAA	57674
rs768733298	snp	G/T	8.43932e-05	0.00649534	missense	RNF213	GRCh38.p7	17:80348185	GCAGCGGAGTGGCTG[G/T]CGCAGGAGTACTTTC	57674
rs768740459	snp	A/G	1.834e-05	0.00302815	missense	RNF213	GRCh38.p7	17:80343311	GTGCTCTTTCACCTG[A/G]ACGTGACCTCCTCAG	57674
rs768754019	snp	A/C/G	3.30427e-05	0.00406454	missense	RNF213	GRCh38.p7	17:80313055	GAAATAATTCAGTCC[A/C/G]AACAGTCTTCCAAGG	57674
rs768762466	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320736	GGACACGGTTGCTCA[C/T]GCCTGTAATCACGGC	57674
rs768762468	snp	C/T	4.94482e-05	0.00497209	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363216	CAGCGTTTCAGAAGC[C/T]GTCTGCAGAACTTTT	57674
rs768772409	in-del	-/C	3.32022e-05	0.00407431	frameshift-variant	RNF213	GRCh38.p7	17:80340218	ACAAGGTCTTCGTCA[-/C]CCCCCCAGGCACCCC	57674
rs768780342	snp	A/G	1.67657e-05	0.00289527	synonymous-codon	RNF213	GRCh38.p7	17:80346702	CGCCATGCAGGGCCC[A/G]GCTGCCTACTCAGAT	57674
rs768786265	snp	A/G	3.3253e-05	0.00407742	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353085	AGGCGGAGCCCCTGG[A/G]GGAGCAGGTGGTGGA	57674
rs768788317	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341360	CCACCCTTCGTTTGC[C/T]ATCTTGTTTCCCTTA	57674
rs768790793	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358374	GAGACGGCAACCTAG[A/G]GTTACTGACCAGGCC	57674
rs768797168	in-del	-/CT	4.97451e-05	0.00498699	intron-variant	RNF213	GRCh38.p7	17:80348319	CTTGTACCCTATCCC[-/CT]GTCACCCAAGAGTCC	57674
rs768800185	snp	A/G	1.67245e-05	0.00289171	intron-variant	RNF213	GRCh38.p7	17:80298526	CTAGATACGTAAGTC[A/G]TAGAGTTGTGCTTAT	57674
rs768806630	snp	C/G	1.64749e-05	0.00287005	stop-gained	RNF213	GRCh38.p7	17:80319302	TTGAAGCCGTGAGCT[C/G]AGCCTGCCAGGTGAA	57674
rs768808093	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80289483	TAATCCCAGCTACTC[A/G]GGAGGCTGTCGCAGG	57674
rs768810923	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80276792	GCGCGGTGGCTCACA[C/G]CTGTCATCCCAGCAC	57674
rs768829345	in-del	-/G	1.67307e-05	0.00289224	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373083	AGCTCAGCAGCCAGC[-/G]GGGGATGGAGTTCGT	57674
rs768848497	snp	C/T	1.64827e-05	0.00287073	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288783	CCTGCCTGCCGGCTC[C/T]AGGAGGCCCTCTCCT	57674
rs768855138	snp	A/G	3.29533e-05	0.00405901	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383723	ATCTCATCAGCCAAG[A/G]TAAGCGTATCAGCTC	57674
rs768876129	snp	A/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352262	AGGATTCTTTCCAGA[A/T]GCAATTAGATTTCTT	57674
rs768895978	snp	G/T	4.60363e-05	0.0047975	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353529	GGCTTGGAACACCGG[G/T]CGGAAGACGGCCATG	57674
rs768900711	snp	A/G	1.65252e-05	0.00287443	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389142	AGAAACCCAGCCCAC[A/G]GACATCCCTCTCCTG	57674
rs768902767	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326044	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	57674
rs768906078	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369650	TTCGTCCAAAAGGGG[C/T]GCTTAAGAGATGCTG	57674
rs768910530	snp	C/T	1.64836e-05	0.0028708	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364426	GAGTGGCGCCCTCTT[C/T]TGACAGAGCCCAGTG	57674
rs768931409	snp	A/G	1.64906e-05	0.00287142	intron-variant	RNF213	GRCh38.p7	17:80307236	CAGTCTCTCCCTCAC[A/G]TGCGGCCCCCGGGGG	57674
rs768936570	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288674	CAATGCAGTTAAAGG[A/G]GCCGGGAAGGAAATG	57674
rs768942288	snp	C/T	1.64795e-05	0.00287045	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379583	CATAAAATGGTACTG[C/T]TCCAGAAGTGGTTCT	57674
rs768949134	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352799	CTGCGCAGGCCCATT[C/T]CAGGGTTTCGGCTTC	57674
rs768953357	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362287	TTTAAACTTCAGTAC[A/C]TAAAAAAGGAGAGTG	57674
rs768954044	snp	C/T	1.6501e-05	0.00287232	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393507	GAGATAGAATTATTT[C/T]CTCAGCTATCTTTGG	57674
rs768969447	snp	G/T	3.41169e-05	0.00413005	intron-variant	RNF213	GRCh38.p7	17:80273438	CTCCCCTCCGCCCCC[G/T]CTCACTCTGCCCAGG	57674
rs768981226	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363049	TTCCCACGGGGAAAA[C/T]ATACCATTTTTGTAA	57674
rs768990872	snp	C/T	1.67097e-05	0.00289043	missense	RNF213	GRCh38.p7	17:80340276	GTCACTACCGGGTCC[C/T]GAAGCAGACCCTGTC	57674
rs768992474	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394953	GTGTGGGGGCCGGGG[A/G]CTGGCTTGCTGAAGT	57674
rs768994726	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80335869	GTAATCCCAGCTACA[C/T]GGGAGGCTGAGGCAA	57674
rs768998304	snp	A/C	1.64768e-05	0.00287021	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361798	GTTTCTTGCCCAGCT[A/C]CATGGAGAGCCGCAG	57674
rs769006355	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80336436	GCATTGCTTAGCAAC[A/G]TTAGGGCAGTGACTG	57674
rs769006726	in-del	-/TCT	1.85679e-05	0.0030469	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376866	CTAGAGCTGTCTCTG[-/TCT]TCTTGTTTTTCAGCA	57674
rs769011045	snp	A/G	1.64792e-05	0.00287042	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354510	AAGAGAGCCAGTTTC[A/G]CCCTCTGGAGTGGTT	57674
rs769045773	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374729	ATTGGAAGTCACGTG[C/T]CCACAGCCTCCAGGG	57674
rs769054838	snp	C/T	3.4313e-05	0.0041419	missense	RNF213	GRCh38.p7	17:80347232	AAATGGTCTTTGCTG[C/T]AGCAAAGGCTTCAAA	57674
rs769064475	snp	A/G	1.64781e-05	0.00287033	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361873	CATGCGTGTGTCAAC[A/G]GAGGAGGAATTAAAG	57674
rs769081079	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284650	ACACCTGATGAGCCC[C/T]GAGCCTGTAGGTGAG	57674
rs769089911	snp	A/G	1.64852e-05	0.00287094	missense	RNF213	GRCh38.p7	17:80346337	AATGCCTTTCTCTCC[A/G]AGTCCAGCGTCAGCA	57674
rs769091450	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387866	TTCTTTGACTGGACG[C/T]ACTTGTTCCTTCCAG	57674
rs769095777	snp	A/G	1.66477e-05	0.00288506	synonymous-codon, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385608	CAAACTGAGGAGATC[A/G]CTTGAGACGAACGGT	57674
rs769101117	in-del	-/TCTCTT	1.69755e-05	0.00291332	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287800	AATAAAGTGAGTGTC[-/TCTCTT]TCTGTTTAGAGCAAA	57674
rs769107793	snp	C/G	4.94214e-05	0.00497074	synonymous-codon	RNF213	GRCh38.p7	17:80344929	CCCGGAGGAATGCCT[C/G]CAGCATTTCCTGTTT	57674
rs769113501	snp	C/T	1.68083e-05	0.00289894	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372702	GCCTCGACAGAGCTG[C/T]AGATTTCCTCTCGGA	57674
rs769116868	snp	A/C/G	3.29969e-05	0.00406172	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388719	CCTGATCCTGTGCAC[A/C/G]GGGCTTTCTGCCTTC	57674
rs769125059	snp	C/T	9.91129e-05	0.00703894	synonymous-codon	RNF213	GRCh38.p7	17:80348271	AGACCTGGAGCGCCA[C/T]GCCATCTTCACAGAG	57674
rs769125434	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80329287	CCTTGTGTGTCTAAA[A/G]ATGTCTGTCCTCTTA	57674
rs769153080	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80267373	ACTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA	57674
rs769157689	snp	A/G			missense	RNF213	GRCh38.p7	17:80325052	CCAGTATCCTTCAGG[A/G]GTTCTCTTACTCTGA	57674
rs769175266	snp	A/G	1.64781e-05	0.00287033	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379687	GAGGCATTGACCACA[A/G]ACCTCGGGACGGCTT	57674
rs769177002	snp	C/G	1.64749e-05	0.00287005	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375779	GCAAGACCCCCCAAA[C/G]CCAGCAGTCAGCCTA	57674
rs769195916	snp	C/T			synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288183	GGACGCTTCCATCCC[C/T]TCTGGGGGCAGAGGC	57674
rs769199487	snp	A/C	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80344866	ACGATTCAATCAAAA[A/C]CAAGACCTAGACACG	57674
rs769221609	snp	A/G	8.23744e-05	0.0064172	missense	RNF213	GRCh38.p7	17:80307137	CCTTAGGATGTTCAG[A/G]ATGTTCAGAACGTTC	57674
rs769227871	snp	A/G	1.65941e-05	0.00288041	missense	RNF213	GRCh38.p7	17:80347121	TCCAGGACCGAGTCC[A/G]AGGGTACTTTGCGTC	57674
rs769243255	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80266207	AGCACTTTGGGAGGC[C/T]GAGGTGAGTAGATCG	57674
rs769243401	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80334501	CTTGCCACACCCCGC[C/T]ACTTCGGAAGCTGTA	57674
rs769244922	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272628	CTGCCTCCCAGCACT[A/G]GCATACTGGGGATCA	57674
rs769254427	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382129	GTGCGTGTCAAAGGA[C/T]CAATCACCATCACAG	57674
rs769256741	snp	G/T	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80290679	AGAGGAGGAGAAGAA[G/T]TTGGGGAGTCAAAAT	57674
rs769267167	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293132	GCACGATCTCGGCTC[A/G]CTACAGCCTCAACCA	57674
rs769268221	snp	A/G/T	0.000495538	0.0157336	synonymous-codon	RNF213	GRCh38.p7	17:80306441	TTACTACCGGCTTCC[A/G/T]GGACTTGAGCAAGTC	57674
rs769271458	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371460	AACCACTCTTCTCAC[A/G]GATTCATGTTTTGGA	57674
rs769284716	snp	C/G	1.66576e-05	0.00288592	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361696	GAGCGCCATGACTTA[C/G]ACGCACTCCAGGCCG	57674
rs769292890	snp	C/T	1.64787e-05	0.00287038	intron-variant	RNF213	GRCh38.p7	17:80307216	AGTAAGTGGAAAGCA[C/T]GATGCAGTCTCTCCC	57674
rs769297332	snp	C/T	1.71516e-05	0.0029284	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354200	CTCTTGCCCCTGCCC[C/T]CACGTGGGCTCTTCC	57674
rs769304311	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319671	GCTCAGTAGGTGTGC[A/G]GGAAGAGACTCCAAA	57674
rs769307918	snp	C/T	1.72907e-05	0.00294025	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354214	CCCACGTGGGCTCTT[C/T]CTGAGGAGTGGGCAT	57674
rs769331499	snp	A/C	3.29462e-05	0.00405857	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385115	TGAAGCAGTTCCAGA[A/C]CGTCCAGCAAGTTGA	57674
rs769346286	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390677	GCTAGAATGAAAAGG[A/C]GTGAGCCACTACACC	57674
rs769352860	snp	C/T	8.23635e-05	0.00641677	missense	RNF213	GRCh38.p7	17:80295747	TGTGTCACCTCCTAA[C/T]CTCAGATGCCAGCTC	57674
rs769367430	in-del	-/GTT	1.66707e-05	0.00288705	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372642	AGAGCCTGCCAACGA[-/GTT]GGCCTCGGTTGAATA	57674
rs769374568	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377825	TTTAAGATAGGGTTT[A/G]AGGGGTGGCGTGCAC	57674
rs769401057	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80297231	TCGAGGCAGGCGGAT[-/C]ACAAGGTCAGGAGTT	57674
rs769402557	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80290587	CGCTGAGCCCGGGTG[A/G]AGGAGTCACCGTGTT	57674
rs769435561	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388531	ACGCTGCAGTTTTCC[A/G]GCTGCAGATTCTGTT	57674
rs769438213	snp	A/G	8.39201e-05	0.00647711	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363330	GTATGGCCCTCCTCC[A/G]CCTGCCCTGAGCAAG	57674
rs769454577	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377611	AGCTTCAGGCAGGTG[C/T]CATGTAACTTAACAA	57674
rs769472502	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80275379	GGTGTTCCTTGAAAA[C/G]ATTGAAGGCAAATGA	57674
rs769483051	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80264721	GCAGACAGTCAAACC[A/T]CAGACCCCCTTACAA	57674
rs769484471	in-del	-/CT	0.000196657	0.00991412	intron-variant	RNF213	GRCh38.p7	17:80339166	TACCCTCTCGCATGG[-/CT]CTGTGAGCCAACCTC	57674
rs769487554	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367833	GCAAGGAGACAGCCA[A/G]CAAGACCCTCAGCAG	57674
rs769490305	snp	A/C/G	8.24377e-05	0.00641976	intron-variant	RNF213	GRCh38.p7	17:80289886	CCTGCCTGAGAGCCC[A/C/G]GCACACCCTCTCCCT	57674
rs769500234	snp	A/G	1.65384e-05	0.00287557	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380990	CCAGAGTTCCCAGGT[A/G]TAACCCAGTGCTGCC	57674
rs769502797	snp	A/G	1.6964e-05	0.00291233	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372604	TCGTTTCCTTAAGGC[A/G]TATTCTCCAGCAAGC	57674
rs769504470	snp	G/T	1.64754e-05	0.00287009	missense	RNF213	GRCh38.p7	17:80346252	CTTTGTCAGCCTCAG[G/T]GACGTGGAGCGCTGT	57674
rs769511279	snp	A/G	1.68764e-05	0.00290481	missense	RNF213	GRCh38.p7	17:80347174	GTGTGTAAGCGCCAG[A/G]ACAAGGAATTCTTCG	57674
rs769511478	snp	C/T	1.66485e-05	0.00288513	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354134	GGGTGGTGCTCCTCC[C/T]GGGCCTCTTGAATGA	57674
rs769522214	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389879	CTCTGGCAGTTCCTG[C/T]CTGCTCATAAGTCTG	57674
rs769533040	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80314160	GTGATGGTGGTGGTG[G/T]AGGTGATGGTGGAGG	57674
rs769533729	snp	A/G	8.35317e-05	0.00646211	intron-variant	RNF213	GRCh38.p7	17:80327767	GGTAACGGCAAAGAG[A/G]CAGGAGGTGGGGAGC	57674
rs769568981	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80327999	AACTGAGTAAGCATC[G/T]AGTCGATACGCACTT	57674
rs769571061	snp	C/T			missense	RNF213	GRCh38.p7	17:80339633	GAGGCCGCCAGGTAC[C/T]GCATGAGGAGAGTCA	57674
rs769584166	in-del	-/T	0.000148275	0.00860904	intron-variant	RNF213	GRCh38.p7	17:80349754	GGCAAGTAATTTGCA[-/T]TTCTTAACTCTGTAG	57674
rs769590286	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80296318	AGCCACCGTGCTGGG[C/T]CTGAATACCCTGCTT	57674
rs769594537	snp	A/G	1.64743e-05	0.00287	missense	RNF213	GRCh38.p7	17:80346161	CCATCAGCCTAGATG[A/G]AAACGGGACTCGCGT	57674
rs769606674	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80356198	GTAGAGGCGAGATTT[C/T]ACCATGTTGGCCAGG	57674
rs769613342	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365348	TAGACACAGTATCAG[C/G]TGATTTCCCACCCAG	57674
rs769614908	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80306934	TTTTTGGTGGAGAAA[A/G]TGGTATAAGTTTAAA	57674
rs769626026	snp	G/T	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389945	TCTTCCTCTCTGCTG[G/T]ACAGAGGGACTGCGC	57674
rs769646816	in-del	-/CA			intron-variant	RNF213	GRCh38.p7	17:80342133	ATATTTGCCCCGTGT[-/CA]CACAGCTCCCCACTG	57674
rs769647534	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80349961	AGCCGCAGCCGTGTG[G/T]CTTCTGCGTGGCGAT	57674
rs769659288	snp	A/G	4.94279e-05	0.00497107	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381599	CAAAAGGCTTTCTGC[A/G]GCAGCACATCCTGAA	57674
rs769678289	snp	A/C	1.65192e-05	0.00287391	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376512	TCTTGGAGCCCCTAA[A/C]GAATCTGGCCTTCTC	57674
rs769697617	snp	A/G	1.69553e-05	0.00291159	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376592	TGGAACACCCCCCAG[A/G]GCTTGTCACTGTAGA	57674
rs769712923	snp	C/T	8.26726e-05	0.0064288	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369781	AGGACACTGTGAACA[C/T]ACAAAATCTCTCTCT	57674
rs769715153	snp	A/C	3.34336e-05	0.00408848	missense	RNF213	GRCh38.p7	17:80346733	CTCTTCCGCAGCCTG[A/C]AGCAGGTCCACCTGG	57674
rs769727870	snp	C/T	3.29701e-05	0.00406005	synonymous-codon	RNF213	GRCh38.p7	17:80347776	TCACCCCAACTTCCG[C/T]CTGATTGTCATTGAA	57674
rs769730543	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80297088	GCTTAAAGTATGAGG[A/G]ATCATTAATATCTTT	57674
rs769733791	snp	C/G	1.64781e-05	0.00287033	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379694	TGACCACAAACCTCG[C/G]GACGGCTTTCATCTG	57674
rs769733795	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360001	CAGTGGCAGATCTTA[C/T]CTTGTGTTTTGAGTG	57674
rs769741580	snp	A/G	1.64784e-05	0.00287035	missense	RNF213	GRCh38.p7	17:80345908	ATTATAGCTGCCTGC[A/G]ATCCATACCGGAAGC	57674
rs769752566	in-del	-/CAAAG			intron-variant	RNF213	GRCh38.p7	17:80277060	GACTCACTCTCAAAA[-/CAAAG]CAAACAAACCAAAAA	57674
rs769753503	snp	C/G	1.65064e-05	0.00287279	utr-variant-5-prime, intron-variant	RNF213	GRCh38.p7	17:80263657	CTCTTGCTTCTGGAT[C/G]TGCAGGGCAGTCCCA	57674
rs769764246	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259341	GGCTTGGTGGCGGGC[A/G]CTTGTAATCCCAGCT	57674
rs769773606	snp	A/G	1.64738e-05	0.00286995	missense	RNF213	GRCh38.p7	17:80345251	GAGCCTCACCCATAC[A/G]TTTTCTTCAATGACG	57674
rs769815732	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384950	TTAAGCTACAAATAC[A/C]AGTCTCGCAGCCAGT	57674
rs769824194	snp	C/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394589	GACAGCTCAGCACAG[C/G]TATTGATATGTTAGA	57674
rs769825240	snp	A/G	3.59978e-05	0.00424236	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373172	AAGCAGCAGGTGAGA[A/G]GCGGGGCCGGGCAGC	57674
rs769826902	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80310951	TTTCAGTTTTCTTGT[A/G]TTAAAGTACCACAGA	57674
rs769838477	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383842	TGGAGCTGCAGGAAA[A/G]GAATTACAGTTGAGT	57674
rs769864948	in-del	-/TAAT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381097	TATGCGTTTTGGAGA[-/TAAT]TAGTCTACAAAGTAA	57674
rs769880979	snp	C/G	6.72868e-05	0.0057999	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287783	GTAGAGTAAATCTAA[C/G]AAATAAAGTGAGTGT	57674
rs769885610	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80322146	TATTTTGCCCCTCAT[-/C]CCCCCCACCCCCCCT	57674
rs769889633	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290925	AGCGATTCTCATGCC[C/T]CAGCTCCCAAGTAGC	57674
rs769893251	snp	A/G	1.66255e-05	0.00288314	missense	RNF213	GRCh38.p7	17:80347340	ACATCTTTCTGGCCA[A/G]TTTGCCCGAGGCCAA	57674
rs769896184	snp	C/T	3.29468e-05	0.00405861	intron-variant	RNF213	GRCh38.p7	17:80306243	TCCGTCCCTATTTCT[C/T]TTATGCAGGAGTTCC	57674
rs769901817	snp	G/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393794	CCAACATTGTTTACA[G/T]TCCAGGAGACTTGTA	57674
rs769904565	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358393	ACTGACCAGGCCAGA[C/T]ACTCCGCCCTGGGCA	57674
rs769921024	snp	A/G	4.9436e-05	0.00497148	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369662	GGGCGCTTAAGAGAT[A/G]CTGCCCAGAGTAGGT	57674
rs769930443	snp	C/T	1.65353e-05	0.00287531	missense	RNF213	GRCh38.p7	17:80346814	TTCCGGCAGTGCGCC[C/T]GCTTTCAGCAGGGGA	57674
rs769932914	in-del	-/TTG			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320336	GAGCATAATGTTTTT[-/TTG]TTGTTGGTGGTGGTG	57674
rs769937205	snp	A/C	2.15079e-05	0.00327925	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353533	TGGAACACCGGGCGG[A/C]AGACGGCCATGAGGA	57674
rs769942624	snp	C/T	3.30825e-05	0.00406696	intron-variant	RNF213	GRCh38.p7	17:80348291	TCTTCACAGAGGTGA[C/T]TGTCTTTCTGCACTT	57674
rs769971071	snp	A/C	1.64885e-05	0.00287123	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375867	CCTCCACCCCACGCC[A/C]GAGGTGAGTAACCGC	57674
rs769975172	snp	C/G	4.95225e-05	0.00497582	intron-variant	RNF213	GRCh38.p7	17:80289655	GTTTGGTTCCTTGTT[C/G]CAGGAAGCTGAGACC	57674
rs769981036	in-del	-/C	1.64727e-05	0.00286986	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377790	CATCCTTGCTCCGTG[-/C]GGAGAGGTGAGTCTT	57674
rs769984642	snp	C/G	1.64806e-05	0.00287054	missense	RNF213	GRCh38.p7	17:80345760	GGCCTTCGCCAATAA[C/G]GACCAACATCAGTTG	57674
rs770013653	in-del	-/TG			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395436	GTAGTGTGTTCAGAC[-/TG]TGCACACAGAAAACA	57674
rs770020927	snp	C/T	1.65211e-05	0.00287407	intron-variant	RNF213	GRCh38.p7	17:80294677	TAGGTCTCCAGGGTT[C/T]TGATGGTCTTAGGTA	57674
rs770035773	snp	C/T	4.94205e-05	0.0049707	synonymous-codon	RNF213	GRCh38.p7	17:80349781	GTAGATCACCACTTT[C/T]TCCAGGCTGCTAACA	57674
rs770036916	snp	G/T	1.67279e-05	0.002892	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386222	GTTGGAACTCCTCTC[G/T]GCTTAAGCATAACCC	57674
rs770040099	snp	C/T	1.64751e-05	0.00287007	intron-variant	RNF213	GRCh38.p7	17:80309007	ATTTCTCTTAACTCT[C/T]TGCGGGGCAGGATTC	57674
rs770040590	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80342793	TTGAGACAGAGTTTC[A/G]CTCTGTCACCCTAAC	57674
rs770042311	snp	A/G	1.6501e-05	0.00287232	intron-variant, missense	RNF213	GRCh38.p7	17:80319424	TCCTCCGCTAACTCA[A/G]AGATTGGGAAGTGGG	57674
rs770042534	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80343649	TAAAACGGTGTATTT[A/T]TGTGTCTAAACATAA	57674
rs770054373	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362719	AGATGTGGACAAATA[C/T]TTGGTTCACAGGGAT	57674
rs770060827	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369974	TAGCTAGTACATGAT[C/T]TTGGGGAGCTTTTTC	57674
rs770087999	in-del	-/A	1.69886e-05	0.00291445	frameshift-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288184	ACGCTTCCATCCCCT[-/A]CTGGGGGCAGAGGCC	57674
rs770089243	snp	C/G	1.65018e-05	0.00287239	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389150	AGCCCACAGACATCC[C/G]TCTCCTGCTTTTCAT	57674
rs770105492	snp	A/G	3.29484e-05	0.00405871	missense	RNF213	GRCh38.p7	17:80344934	AGGAATGCCTCCAGC[A/G]TTTCCTGTTTCACTG	57674
rs770115601	snp	A/T	3.30207e-05	0.00406316	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380808	GCCTCAGCCTCTGTC[A/T]TGTGTTCTCTCGTTC	57674
rs770125513	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80317391	GTGGGCAGGGATGGG[A/G]TGAATCACAGCTCCG	57674
rs770129211	snp	A/G	6.32451e-05	0.00562304	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381753	GGGCAAGGGCTGGGC[A/G]GGGATCACACAGCAC	57674
rs770129719	snp	A/G	3.29685e-05	0.00405995	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354532	GGAGTGGTTGGCAAG[A/G]GAAGCCTGCAACCAG	57674
rs770168815	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80326099	AAGTAGCTGGGATTA[C/T]AGATGTGAGCCACTG	57674
rs770175256	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80338678	ATTTAAAAAAATTAA[A/C]ACAGTCCAGGCATCA	57674
rs770188341	snp	C/T			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398953	GTAAACAAGGGCATA[C/T]CCCGAAAGCACTGAG	57674
rs770203089	snp	C/T	4.94238e-05	0.00497086	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376269	CACAATATTCTTTGA[C/T]ACATCTTAATGTTAA	57674
rs770229538	snp	C/G	1.66446e-05	0.00288479	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354613	AGGAGTGGCTCCAAT[C/G]TGGTGGCAGCATGGG	57674
rs770230709	snp	A/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353294	GCCAGCCATGGAAGT[A/G]AGCACCTAGAACACG	57674
rs770232403	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80273158	GTGAATCTCTCCATG[C/T]ACTCGTGGGGAGGAT	57674
rs770233838	snp	A/G	6.71152e-05	0.0057925	synonymous-codon, intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80385617	GAGATCGCTTGAGAC[A/G]AACGGTTAGTATCCT	57674
rs770234074	snp	A/G	1.65056e-05	0.00287272	missense	RNF213	GRCh38.p7	17:80347432	AAGGTGCCGGGTGGA[A/G]AGCAGGAAGATGCTG	57674
rs770236636	snp	C/G	2.59091e-05	0.00359915	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372932	CCTACAATAAATGCC[C/G]TAAGTCACCAGCCAC	57674
rs770288764	snp	C/T	6.58903e-05	0.00573941	synonymous-codon	RNF213	GRCh38.p7	17:80290597	GGGTGGAGGAGTCAC[C/T]GTGTTCTTCCACGCC	57674
rs770299257	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80316783	CCGAAGAGGGAGCAC[A/G]GAGGAGAGAGGAAGA	57674
rs770306523	snp	A/G	3.30033e-05	0.00406209	missense	RNF213	GRCh38.p7	17:80346418	GGGGTGTGTTACCAT[A/G]CCTCTTTAGAAAAGA	57674
rs770319999	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80284766	TCCCTCGTGCCACAC[A/G]GTGGCTTCCCCTGTG	57674
rs770321696	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388028	GCAGTGGCGCAATCT[C/G]AGCTTGCTGCAAGCT	57674
rs770322227	snp	G/T	1.64762e-05	0.00287016	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389270	TAGAAGTCACTCTGG[G/T]GTTTCTGAGCACAGC	57674
rs770358835	snp	A/G	1.64838e-05	0.00287083	synonymous-codon, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351760	TTTCATCACAAAACT[A/G]TCCCGGGTGGGAAGA	57674
rs770366514	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80293462	ATACATTTAAATATG[C/G]AATTCTATATATATA	57674
rs770374087	snp	C/G	1.64732e-05	0.0028699	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367860	GCAGGTGAGACCTTA[C/G]GTTTGGATCTGTGAA	57674
rs770377223	snp	C/T	0.000460858	0.0151729	intron-variant	RNF213	GRCh38.p7	17:80317168	TGAGAGTGGGTGTGA[C/T]CTGTGTGCGGGTTTT	57674
rs770392866	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80267512	AGCCTTATTGTGATA[C/T]GGAGAGAGTTTGCAA	57674
rs770403387	snp	C/G	0.00011763	0.0076682	intron-variant	RNF213	GRCh38.p7	17:80290779	GGGAAGGCATAGGAT[C/G]CCCAGCCTGTGACAC	57674
rs770408880	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362198	GAAAAAAATTAAATA[C/T]GTAACTAACCCTACA	57674
rs770415374	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372505	ATCCTTTTCTTTCTT[A/G]TTCCTTGTTCCTCAG	57674
rs770417308	snp	A/G	4.94254e-05	0.00497094	missense	RNF213	GRCh38.p7	17:80346256	GTCAGCCTCAGGGAC[A/G]TGGAGCGCTGTGTGA	57674
rs770419808	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80334028	GTGGGGCTGCTGGGA[C/T]GGTCAGTGCTTGCAG	57674
rs770425328	snp	C/G	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381624	CCTGAAGGACCTGGA[C/G]CAGTTGGCCAAGATG	57674
rs770436228	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397691	GGGAGCTCAGTTGTT[A/G]GAGACATGAGTCTTG	57674
rs770443490	snp	C/T	0.000123039	0.00784247	synonymous-codon	RNF213	GRCh38.p7	17:80327823	CTATTCAGGAACCGA[C/T]GAGAAAATACTAGCA	57674
rs770451973	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389959	GGACAGAGGGACTGC[A/G]CTCCCTTCTCCCTGC	57674
rs770456826	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373762	AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA	57674
rs770463091	snp	C/T	6.59131e-05	0.0057404	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381533	CTGAACACTCTGTTC[C/T]GTTGCCCCCACAGGC	57674
rs770465314	snp	C/T	1.64928e-05	0.00287161	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368116	CCTTGCCAGACGAAT[C/T]CTCTCCAGCTGTTTC	57674
rs770471430	snp	A/C	0.000116381	0.00762737	missense	RNF213	GRCh38.p7	17:80332437	AATAAATACACGGAC[A/C]TGGATTCAGAACTTA	57674
rs770482916	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277848	GGAGCCAAGGGAGGC[A/G]GCCCCAGAAGCTGAG	57674
rs770487709	snp	A/G	3.3465e-05	0.0040904	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373029	AGCAGTTCTGTATCC[A/G]GGTGGAGAACGACTG	57674
rs770499998	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	RNF213	GRCh38.p7	17:80295721	TTTATTAGAAGGCAG[C/T]CTGGACTGGTTGTGT	57674
rs770505224	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383364	GAATGTAATGTACGA[A/G]GTAGAGAAATAAACT	57674
rs770518080	snp	A/G	1.64855e-05	0.00287097	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385214	ACTGTCCCGCATTTG[A/G]CGGTTCGAAAGGATC	57674
rs770543379	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80306713	AAAAATTAGCTGGGC[G/T]TGGTGGTGGGTACCT	57674
rs770544917	snp	A/C/G	6.58928e-05	0.00573957	missense	RNF213	GRCh38.p7	17:80345266	GTTTTCTTCAATGAC[A/C/G]ACCACACAACCATGA	57674
rs770546402	snp	A/G	1.68151e-05	0.00289953	synonymous-codon	RNF213	GRCh38.p7	17:80347290	ACAGGCTGTCCTTAG[A/G]AACTTCAGTGGCAAG	57674
rs770554463	snp	C/T	7.20089e-05	0.00599994	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288063	GCCCACCGAGGTTGG[C/T]GACAGCCCCCTGCAG	57674
rs770562324	snp	A/C/G	8.31627e-05	0.00644789	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358491	AAAGGTGAGTGGAAG[A/C/G]CTTTCTTTCCCTGGG	57674
rs770574711	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	RNF213	GRCh38.p7	17:80306360	TCACCTGGTTATGTA[C/T]ATGGAAAACTTCATT	57674
rs770577008	in-del	-/TTTTTTTTTTCTTT	1.65096e-05	0.00287306	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352906	AGCCGGGAAAGACAC[-/TTTTTTTTTTCTTT]AAAGACAGTTGTGGG	57674
rs770588058	snp	C/T	1.65789e-05	0.0028791	missense	RNF213	GRCh38.p7	17:80295641	TTTTTGCCTGTGGAC[C/T]GCCCAGTGAGGAGTA	57674
rs770593558	snp	C/T	6.59544e-05	0.0057422	synonymous-codon	RNF213	GRCh38.p7	17:80347803	TGAAGAGAAAGACGT[C/T]GTGTACAAACACTTT	57674
rs770621465	snp	A/G	0.000115667	0.00760396	synonymous-codon	RNF213	GRCh38.p7	17:80332082	CACCGTGACAGTGAG[A/G]CTGTCCACCTCCTCG	57674
rs770630967	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390542	GCTGGGACTACAGGC[A/G]TGTACCACCATGCCT	57674
rs770646910	snp	G/T	2.64148e-05	0.00363411	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351636	TTTGCTTGTTTTTGT[G/T]TGTGTGTTTGTTTTT	57674
rs770646963	snp	A/G	1.67335e-05	0.00289248	missense	RNF213	GRCh38.p7	17:80346667	AGCTCCAAGTCTCTC[A/G]CCAAGACCATCGTGG	57674
rs770647267	snp	A/T	3.31186e-05	0.00406918	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376524	TAAAGAATCTGGCCT[A/T]CTCCCCAGCCACCAT	57674
rs770650044	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80321212	CATAGCCTGAAGGTA[A/G]TTTTATACAATATTT	57674
rs770660616	snp	A/C	1.69502e-05	0.00291115	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376590	ACTGGAACACCCCCC[A/C]GAGCTTGTCACTGTA	57674
rs770666771	snp	C/T	0.00042264	0.0145307	intron-variant	RNF213	GRCh38.p7	17:80317138	TTCATGGGAGTGTGC[C/T]GTGGCATTTAGTCGT	57674
rs770679506	in-del	-/CCTT	1.65323e-05	0.00287505	intron-variant	RNF213	GRCh38.p7	17:80349919	CGGTGAGGTTCCCTG[-/CCTT]CCTTCCCTGCTGCCC	57674
rs770683115	snp	A/G	1.64985e-05	0.0028721	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386692	TTCTGCCCCTCAGCT[A/G]TTCCGTGGATGCCGC	57674
rs770683839	snp	A/G	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80290655	CCTGACCTCCATAAA[A/G]TCTTCATCAGAGGAG	57674
rs770684401	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367318	ATAATGTTTTGTTTC[C/T]CTAAAAAATGATCTA	57674
rs770712988	snp	A/T	1.6473e-05	0.00286988	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383752	TCTAACCCTGTGGCC[A/T]AAATAATATATGGTG	57674
rs770719543	snp	A/C/T	1.64914e-05	0.00287149	intron-variant	RNF213	GRCh38.p7	17:80319170	AAAGCTCTGAAACCA[A/C/T]CCCCCTTTGATTTTT	57674
rs770726133	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328646	TCTTTTAGATTCTTC[C/T]TTTTGGTATTTATGT	57674
rs770730576	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357180	CCTCAGCCTCCCAAC[A/G]TGCTGGGATTAGACG	57674
rs770746482	in-del	-/TTTA			intron-variant	RNF213	GRCh38.p7	17:80340975	CACCCAGCTAATTTT[-/TTTA]TTTATTTTTAGTAGA	57674
rs770754192	snp	C/G	1.66846e-05	0.00288826	missense	RNF213	GRCh38.p7	17:80346748	AAGCAGGTCCACCTG[C/G]TGTCCTTCCAGTGCA	57674
rs770780342	snp	A/C	3.29935e-05	0.00406149	intron-variant	RNF213	GRCh38.p7	17:80294712	CTTGTTCCTTCTGTC[A/C]CTCTTAGACTGGCAT	57674
rs770790542	snp	C/G	1.64749e-05	0.00287005	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288716	CCAGAGAATGAAACA[C/G]CCACCAGCAACCACT	57674
rs770794040	snp	A/G	4.94181e-05	0.00497057	missense	RNF213	GRCh38.p7	17:80306253	TTTCTCTTATGCAGG[A/G]GTTCCCTACTTCAGT	57674
rs770799233	snp	G/T	1.64727e-05	0.00286986	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383852	GGAAAAGAATTACAG[G/T]TGAGTACCTCCAGCA	57674
rs770808377	snp	C/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390053	GTACAAAGCGGATCT[C/G]AGCCCGGAAAATGCT	57674
rs770808752	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391581	TTTTGCGCTTTGTCT[C/G]TGTAATGGTTGTGAG	57674
rs770814113	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80339731	GCAGTCCATGAGGTG[C/T]CTTCCTGCCTTCCTG	57674
rs770826997	snp	C/G	1.64773e-05	0.00287026	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374449	CCCCAACTAACCTCT[C/G]TATTCCAGGGGCTGC	57674
rs770842568	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80312718	TGGGCACAGCCTGGG[A/G]ACCTGCTCATTGGCA	57674
rs770855081	snp	A/G	0.000696621	0.0186501	intron-variant	RNF213	GRCh38.p7	17:80338022	CATCTTTGCAGTGGC[A/G]CTAAGCTGGTGGTGT	57674
rs770855279	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80340951	CTAGGACTACAGGCA[G/T]GCACCAGTACACCCA	57674
rs770859564	snp	A/G	0.000115696	0.0076049	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393538	ATGACTTTGGAGAGA[A/G]GACTCCTCTCTCCTC	57674
rs770869601	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353645	GGTGGGAAAGGAAAC[C/T]TCTGAACTCGGAGGC	57674
rs770871308	snp	A/C	1.65176e-05	0.00287376	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364578	TGGGCTGGCCTCAGC[A/C]CATGCACGGATCCAC	57674
rs770872622	snp	A/G	3.36366e-05	0.00410088	intron-variant	RNF213	GRCh38.p7	17:80263810	CTGGTGGAGGCTGGG[A/G]CAGTGGGGACCCCTG	57674
rs770879862	snp	A/T	1.64787e-05	0.00287038	missense	RNF213	GRCh38.p7	17:80294954	AACAGCCTATGATTT[A/T]TGAAGGACAGGCACA	57674
rs770880299	snp	C/T			synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287901	CCTTTCTCCTGCCAG[C/T]CCCTGTCACCTGACT	57674
rs770898581	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390834	TTGGGAGGCCGAGGT[A/G]GGTGGATCACCTGAG	57674
rs770946394	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259954	AGGGTCCCCTCTGGA[A/G]TGCGCAGAGGGGCGC	57674
rs770950262	snp	G/T	3.357e-05	0.00409681	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376939	GCTCGGAGGTGGAAG[G/T]GTCTGGAGCGAGTCC	57674
rs770958199	snp	C/T	1.6489e-05	0.00287128	synonymous-codon	RNF213	GRCh38.p7	17:80289676	AGCTGAGACCAAGAC[C/T]AAGGACGAGATGGCT	57674
rs770989046	snp	C/T	4.94189e-05	0.00497062	synonymous-codon	RNF213	GRCh38.p7	17:80309111	GCTACTTAAGTTTTA[C/T]GAGCTGCCAGCCTTA	57674
rs770990099	in-del	-/AAAG	3.29506e-05	0.00405884	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383890	GAACAGAAAAATGGC[-/AAAG]AAAGAGTGCCCATCC	57674
rs770992440	snp	A/G	1.68621e-05	0.00290358	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287791	AATCTAAGAAATAAA[A/G]TGAGTGTCTCTCTTT	57674
rs771001779	snp	A/G	1.651e-05	0.0028731	missense	RNF213	GRCh38.p7	17:80346443	AAAAGAAAGACTCAT[A/G]TCGGAAAGCCATCGC	57674
rs771010241	snp	C/T	6.79279e-05	0.00582746	intron-variant	RNF213	GRCh38.p7	17:80340383	GGCAGGGTGGGCAGG[C/T]CCCGTCTCCCAGGGA	57674
rs771015395	in-del	-/CC			intron-variant	RNF213	GRCh38.p7	17:80322146	ATTTTGCCCCTCATC[-/CC]CCCCCCACCCCCCCT	57674
rs771017849	snp	C/T	6.60317e-05	0.00574556	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380811	TCAGCCTCTGTCTTG[C/T]GTTCTCTCGTTCTTT	57674
rs771020198	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397697	TCAGTTGTTGGAGAC[A/G]TGAGTCTTGCCGAAG	57674
rs771024450	in-del	-/C	9.21973e-05	0.00678897	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389406	ATCAGCACAGCCCCT[-/C]ACCCTGGTCTCCTGC	57674
rs771028681	in-del	-/AGAA			intron-variant	RNF213	GRCh38.p7	17:80341748	GTCTTTTAAAAAAAG[-/AGAA]AGAAAGAAAGAAAGA	57674
rs771036015	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80269719	ATGTATCTATCCATT[C/T]ATCTATCCCATCTTA	57674
rs771039919	in-del	-/AC			intron-variant	RNF213	GRCh38.p7	17:80272950	CGCTGACATCCTAGT[-/AC]AGAGTCAGGTGAATC	57674
rs771047598	snp	C/G	3.30284e-05	0.00406363	intron-variant, missense	RNF213	GRCh38.p7	17:80319440	AGATTGGGAAGTGGG[C/G]ACCCTCCTCCCTCGC	57674
rs771053566	snp	C/T	1.6489e-05	0.00287128	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364506	ACCGAGAGCCGCGTC[C/T]CCGAGTTACAGGGGC	57674
rs771058773	snp	C/G	1.64776e-05	0.00287028	missense	RNF213	GRCh38.p7	17:80345999	AGGAGACGGCCGACA[C/G]GCTGGGCTCCATTCC	57674
rs771059489	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80311313	CAGGGTTGACGGACA[C/G]TTGGAGAACAAGGTG	57674
rs771060238	snp	C/G	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80294848	GCCGCTGCGCTCATG[C/G]TGGACAGCACCTTCA	57674
rs771061203	snp	C/T	8.68734e-05	0.00659008	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287893	TCCTTGCCCCTTTCT[C/T]CTGCCAGCCCCTGTC	57674
rs771084856	snp	A/C	1.67293e-05	0.00289212	missense	RNF213	GRCh38.p7	17:80289746	CCTGAAGACCTCAAG[A/C]AGCCAGAGGGGAAGA	57674
rs771100636	snp	C/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80344942	CTCCAGCATTTCCTG[C/T]TTCACTGCGGGGTAA	57674
rs771115668	in-del	-/T	1.64781e-05	0.00287033	frameshift-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288650	AGTTGATGCTGTAGC[-/T]GAGCCAGCCAATGCA	57674
rs771126061	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80280507	GTCCCAGGCTGGAGC[C/G]CAGTGGCAAAATCAT	57674
rs771129545	snp	C/G	1.64868e-05	0.00287109	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389297	CAGCTGGTGGGGATC[C/G]AAACATGCAGCTGAA	57674
rs771132706	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80291214	TTGGTGTCATATTCC[A/G]TCATGGACCTTTTTC	57674
rs771138220	snp	C/T			missense	RNF213	GRCh38.p7	17:80340090	AGGTGGCACGCCAAG[C/T]GGAGGAGCTTTTCCA	57674
rs771147762	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80323548	TTTTTTTTTCCCCTG[G/T]TAGACAGAGTCTCGC	57674
rs771176350	snp	C/T	1.648e-05	0.0028705	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363181	AAGAGGTTTCCTTAC[C/T]GTGGGTGCACCTTGC	57674
rs771183046	snp	A/C	3.29473e-05	0.00405864	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389206	GTCATTAGTGCCATC[A/C]GTGGACAGCTGCAGT	57674
rs771183294	snp	A/G	1.64849e-05	0.00287092	intron-variant	RNF213	GRCh38.p7	17:80309194	GAGTCAACACACAAG[A/G]TATCACACCCGGGAT	57674
rs771185384	snp	C/T	3.42683e-05	0.0041392	intron-variant	RNF213	GRCh38.p7	17:80298317	GATCTTTATTCCCTT[C/T]CAGCTGGCGGCTGTA	57674
rs771195797	in-del	-/TAAGT	1.66664e-05	0.00288668	splice-donor-variant	RNF213	GRCh38.p7	17:80298519	CAAATGCTAGATACG[-/TAAGT]TAAGTCGTAGAGTTG	57674
rs771211275	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80350053	TCTCTCCCAGCATCC[C/T]TCTCATCTCCATCAT	57674
rs771213224	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370685	CTCCCACTACACACC[A/G]GAGTAGACAGTTGCC	57674
rs771217556	snp	A/G	4.99413e-05	0.00499682	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386259	TTAAAGGTGAGATCA[A/G]CCTACCCAAAGACTA	57674
rs771219424	snp	A/G			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360797	ATCTTTCATACATGC[A/G]ATAGTCTTTTCCACG	57674
rs771221903	snp	A/G	1.64898e-05	0.00287135	missense	RNF213	GRCh38.p7	17:80347534	GGGGACCAGCAGCCG[A/G]AGATTATTTTTGGTT	57674
rs771224297	snp	A/T	1.6617e-05	0.00288239	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358259	GGTTCCTCTGACCCG[A/T]GGTGGCCCATCTCTC	57674
rs771228662	snp	A/C	1.64806e-05	0.00287054	intron-variant	RNF213	GRCh38.p7	17:80291606	AATTTTGGATAGCCA[A/C]CCGTATCCTGTTCAT	57674
rs771241585	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376331	AGCAAATTCATTGGC[A/G]AATGCAAGATCCTTT	57674
rs771252118	in-del	-/AAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382821	CATTAAGTTGGTGGT[-/AAC]AACAGGAACTACTTC	57674
rs771254197	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80317536	GATTTTTCCTGACCC[C/T]TTCGTTGGACTTGCG	57674
rs771261410	in-del	-/AG			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319907	CAGCCTTGCGGCCAC[-/AG]GGGAAGTCCAGAAAC	57674
rs771268044	snp	A/C	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80291677	ATTGTCTGCATTTCC[A/C]AGAAGCACCTAGATA	57674
rs771270426	snp	A/G	1.65119e-05	0.00287327	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352892	TTAGGGCTGAGCAGC[A/G]GCCGGGAAAGACACA	57674
rs771275620	snp	A/C			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355091	GAGGAAGGAGGGGTG[A/C]TCTGGGCCCCAGACA	57674
rs771279161	snp	A/G	3.29696e-05	0.00406001	missense	RNF213	GRCh38.p7	17:80349897	AGTACTCATTCCTCA[A/G]AGAAGTCCGGTGAGG	57674
rs771281594	snp	A/G	1.64876e-05	0.00287116	missense	RNF213	GRCh38.p7	17:80345420	AGAGGGTGCCCTTCA[A/G]TGTCGACTTTGATAA	57674
rs771281742	snp	A/C	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377730	ATTGGGTGAAACCTC[A/C]TTAGCCAATGTGTGT	57674
rs771285951	in-del	-/TGATGGTGA			intron-variant	RNF213	GRCh38.p7	17:80314464	TGGAGGTGATGGTGG[-/TGATGGTGA]TGGTGGAGGTACTGG	57674
rs771294043	snp	C/T	0.000121381	0.00778948	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386877	CTCCAGGGCAAGCCC[C/T]GGCTGAGCCTCAAGG	57674
rs771304386	snp	C/T	1.64751e-05	0.00287007	missense	RNF213	GRCh38.p7	17:80345644	TTCCTTAGCGACCTG[C/T]GGCGTGGTGGTACCA	57674
rs771308296	snp	C/T	1.65165e-05	0.00287367	missense	RNF213	GRCh38.p7	17:80298425	GTATGGAGCTGGCCC[C/T]GCGGCACAAGGATGC	57674
rs771311592	snp	C/T	1.64993e-05	0.00287218	missense	RNF213	GRCh38.p7	17:80347453	GAAGATGCTGAGTCC[C/T]GCTACTTACTCGTGC	57674
rs771318645	snp	C/G	1.64779e-05	0.00287031	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288609	CATTTTGTCACCTTG[C/G]CTCTGGTGTTTGGGG	57674
rs771318958	snp	C/T	1.65154e-05	0.00287358	missense	RNF213	GRCh38.p7	17:80348116	TCGATCCTGCTGAAC[C/T]GCGCTACGCCCGATG	57674
rs771319096	snp	A/G	9.03122e-05	0.00671922	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376974	GTACAGTAAGTGTTG[A/G]GGTCTAGATGACCCC	57674
rs771323191	in-del	-/GGGGGCTTACAGGGGGAAGAAGCGGGGTGGACGGGAA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355513	GGGGTGACCGGGAAT[lengthTooLong]TGGGGGCTTATGGAG	57674
rs771331439	snp	C/G	1.67058e-05	0.00289009	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373036	CTGTATCCGGGTGGA[C/G]AACGACTGGCACCGG	57674
rs771354087	snp	A/G	4.48019e-05	0.00473275	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381764	GGGCGGGGATCACAC[A/G]GCACAACGGCAGCGC	57674
rs771355185	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355981	TTTTCATTTCCCTCC[A/G]TTCCTCCTTGTGGAC	57674
rs771375942	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80331849	AGGCCAAGCGGGGAG[A/G]GAAAGACCTGTGAAC	57674
rs771379367	snp	C/G	3.35008e-05	0.00409259	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390212	GTATGGATTTGCACA[C/G]CTATGGGGCGGGGCA	57674
rs771388291	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80273855	AAACTCCTGACCTCA[A/G]GAGATCCACCCACCT	57674
rs771396979	snp	A/G	1.66128e-05	0.00288204	missense	RNF213	GRCh38.p7	17:80346508	CTGCTTCTGGATGAA[A/G]TAACACGGGCACAGG	57674
rs771407521	snp	A/T	1.81243e-05	0.00301029	missense	RNF213	GRCh38.p7	17:80317245	GGCTGGAAGGAGTCG[A/T]TGCTGGGAGACATGG	57674
rs771417979	snp	A/G	0.00011411	0.0075526	missense	RNF213	GRCh38.p7	17:80334195	CTCCAGGACATCAGC[A/G]AGGCCCGGTGCAAGG	57674
rs771430826	snp	A/C	1.65244e-05	0.00287436	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390140	GCACGAAATGATAAT[A/C]TTGAAACTAAAGAAC	57674
rs771437070	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389634	ACAGCGTGATGTGAG[C/T]GGGCTGTGAGGTGCC	57674
rs771459701	snp	C/T	1.64732e-05	0.0028699	intron-variant	RNF213	GRCh38.p7	17:80343829	CCATCGTGTCGTGTG[C/T]TTACACCTCGTGCGA	57674
rs771502456	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260546	CAGGGCGGGGCCGGC[A/G]GCGGCGGCGGCGGGC	57674
rs771504450	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80285549	GGCCTCTTGCTTCCC[C/T]CTCTCAGCAGGTCCC	57674
rs771507242	in-del	-/ATCTT			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359995	TGGCATCAGTGGCAG[-/ATCTT]ATCTTGTGTTTTGAG	57674
rs771511089	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80284913	AATCCCCCAGTGGGT[C/T]CCTATGGCCAGGATG	57674
rs771533041	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388926	GATGCATGGCCATGC[C/G]TGCTGAAGCGGGAAG	57674
rs771534016	snp	A/T	1.72528e-05	0.00293703	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288358	GCAGGGGCCTCAGCC[A/T]CTATGGTGAGTCATC	57674
rs771547942	snp	C/G	3.29506e-05	0.00405884	missense	RNF213	GRCh38.p7	17:80345361	TGGGAAGGTCATCAA[C/G]AGAGACGTCATGACC	57674
rs771548492	snp	G/T	1.8269e-05	0.00302228	splice-donor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363791	CATCAGGGAAGTCAG[G/T]TGAGACCCAGGAGCC	57674
rs771572747	snp	G/T	1.64868e-05	0.00287109	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368099	CCCCTACTGTTTAAC[G/T]GCCTTGCCAGACGAA	57674
rs771577572	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388816	GTTTCTGCGGCCTCC[C/T]TTACAGAGAGCAAGC	57674
rs771578676	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364315	GCTTGCTTGTAATCC[C/T]AGCCGCTGGGCCTGG	57674
rs771580950	snp	A/G	1.96616e-05	0.00313535	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376839	CAGCACCCAGGTGAC[A/G]AGCTCACTTATCTAG	57674
rs771584949	snp	C/T	1.65072e-05	0.00287286	stop-gained	RNF213	GRCh38.p7	17:80345488	ACCTTAGGGATCCCC[C/T]AGGCCACCGACCCCG	57674
rs771592361	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80296043	GTTTTCCCCCCAGAC[A/G]GCGTCTCACTCTGTG	57674
rs771592711	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80309424	GGGAGTTAATGTGTG[A/G]CCATCAGCTGGTCAT	57674
rs771602067	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383655	CACTTCCAGAATTTT[C/T]TTTTTCATTTTCTCC	57674
rs771602137	snp	A/G	1.65157e-05	0.0028736	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381655	CTGGGACACAGTGCC[A/G]ACGAGACCATCGGCG	57674
rs771603843	snp	C/T	1.64762e-05	0.00287016	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369560	AGTTTCTTCGTAGAC[C/T]TGGTGTCCACCATTT	57674
rs771608211	snp	C/G	1.70502e-05	0.00291972	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363746	CTCCGATGAGCACAT[C/G]CAAGGCAGCGGGAGC	57674
rs771616609	snp	C/G			downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399243	CTACCATACCTAGGA[C/G]GAACTCCCTTCAGGA	57674
rs771616975	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80268147	TTTTTAAGGCCGAGT[A/G]GTGTTCCATTATGTA	57674
rs771624513	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80327726	AGGAAGTGGGGGCAG[A/G]ACAAGAGGTTATCTG	57674
rs771630272	in-del	-/AC	1.64773e-05	0.00287026	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369543	TCCGGCAGATGTGCA[-/AC]AGTTTCTTCGTAGAC	57674
rs771631512	snp	C/G	1.65075e-05	0.00287289	synonymous-codon	RNF213	GRCh38.p7	17:80263726	CAAGGAGGAAACCCC[C/G]AAGTTCTGCAGCCAG	57674
rs771635323	snp	C/T	1.64993e-05	0.00287218	missense	RNF213	GRCh38.p7	17:80346407	TGCTGGCCATCGGGG[C/T]GTGTTACCATGCCTC	57674
rs771661256	snp	A/G	1.6546e-05	0.00287624	intron-variant	RNF213	GRCh38.p7	17:80290751	TGTCTGTAGGCTTGG[A/G]AGGAATCCCTCAGGG	57674
rs771680525	snp	C/T	1.71e-05	0.00292399	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376956	TCTGGAGCGAGTCCA[C/T]TGGTACAGTAAGTGT	57674
rs771684029	in-del	-/ATGGCAGGTGTGGAGCGTGGCGTGCAC	6.664e-05	0.00577196	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353108	GTGGTGGAAGGGCAG[-/ATGGCAGGTGTGGAGCGTGGCGTGCAC]ATGGCACTAGGAGCA	57674
rs771696784	snp	A/G	1.65034e-05	0.00287253	synonymous-codon	RNF213	GRCh38.p7	17:80294973	AGGACAGGCACAGCT[A/G]TGGACCGATTTGCAG	57674
rs771702964	snp	A/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353658	ACCTCTGAACTCGGA[A/G]GCAGTGATGTAAGTT	57674
rs771708425	snp	C/T	6.6235e-05	0.0057544	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360041	AAACCCTCTTCTTAT[C/T]ATCCCTCACCTTATT	57674
rs771713613	snp	A/G	4.94189e-05	0.00497062	stop-gained	RNF213	GRCh38.p7	17:80343933	TAAATGGGAAAATGT[A/G]GCTTCGGAACCCCTG	57674
rs771738412	snp	C/T	1.65737e-05	0.00287864	missense	RNF213	GRCh38.p7	17:80346881	ATGAGGTGGGGCTGG[C/T]GGAAGACTCACCCAA	57674
rs771759700	snp	A/G	1.66632e-05	0.0028864	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363645	ATGGCCTGCACGGAG[A/G]TGCTGACAAGAAACA	57674
rs771764682	snp	C/T	1.69461e-05	0.0029108	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288224	AGGGGACCGGTCCCC[C/T]CACCTCTGCTGGTGA	57674
rs771767298	snp	C/T	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389978	CCTTCTCCCTGCAGG[C/T]TTTAATGCTTCATTT	57674
rs771768618	snp	A/G	1.64939e-05	0.0028717	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374539	CTCCGTGATGCTGTG[A/G]CCAAAGCTGTCCTCG	57674
rs771771889	in-del	-/AG	1.64762e-05	0.00287016	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358358	ATATCATTCATCGAC[-/AG]AGACGGCAACCTAGA	57674
rs771789535	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80324963	GAGTAGGTAATTTGC[A/T]TTTGTTATTTCAAAA	57674
rs771794678	snp	A/G	1.65734e-05	0.00287862	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360113	CACATGAACCTTTCC[A/G]AGAACGCTTCCAACA	57674
rs771800984	snp	G/T	1.6888e-05	0.00290581	missense	RNF213	GRCh38.p7	17:80346971	CCCCCCACAAAAAGG[G/T]CGGCTTCGTGGGCAT	57674
rs771805166	snp	C/T	6.58913e-05	0.00573945	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383868	TGAGTACCTCCAGCA[C/T]ATTGTGGAACAGAAA	57674
rs771806016	snp	A/G	3.30218e-05	0.00406323	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386802	CAGGTGGAGGAGGGC[A/G]GAGAGACCGTGCAGG	57674
rs771815793	in-del	-/CGG			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260542	CGGGCAGGGCGGGGC[-/CGG]CGGCGGCGGCGGCGG	57674
rs771824327	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80308365	CCCTCCATCAACTCT[C/G]CTCTTAAGCTCCTCC	57674
rs771831019	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374621	GCTTCTCTCTGATAC[C/T]AGGTGGCATCCCTTG	57674
rs771832634	snp	A/G	3.31055e-05	0.00406837	synonymous-codon	RNF213	GRCh38.p7	17:80348004	CATCGGCTACCACTC[A/G]GACGCCTGCGCGTCT	57674
rs771847475	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359039	GGAGACAGTGCGCTG[C/G]GAACAGCCCCACAAT	57674
rs771857552	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374171	ATGACTTGAGCCACC[C/T]GGCCTCAGGTGTGGT	57674
rs771857582	snp	A/T	1.64741e-05	0.00286998	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390063	GATCTGAGCCCGGAA[A/T]ATGCTAAGCTCCTCA	57674
rs771864507	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320020	TTTTCGTTAACTCTT[C/T]GTTGAGATATTGTTC	57674
rs771882010	snp	A/G			splice-acceptor-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351684	TTTTTTCTTTAAATA[A/G]GTATTCTGTTATAAA	57674
rs771884186	snp	A/G	4.9928e-05	0.00499615	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351829	AACATCAGTCAGGGT[A/G]TTTATTTATGTATTT	57674
rs771921862	snp	C/G	1.64808e-05	0.00287057	missense	RNF213	GRCh38.p7	17:80346053	TCCATGCTCTGCCCC[C/G]GAGCCTGATTCCTCT	57674
rs771922492	snp	C/G	6.58935e-05	0.00573955	missense	RNF213	GRCh38.p7	17:80294874	CTTCAGCATCCTGCA[C/G]ACCTGGGACACCATC	57674
rs771929474	snp	A/G	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80345062	AGTTTTATTGGCGAC[A/G]CACTGAGGGGCTTCA	57674
rs771929756	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80265999	CCATGGCCAGGCTGG[-/A]GACATTGAGTTCCAA	57674
rs771932090	snp	C/T	3.29457e-05	0.00405854	missense	RNF213	GRCh38.p7	17:80349822	GTGAAATTTTAGAAT[C/T]AGAGGTCACAGGCAG	57674
rs771935182	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80279247	TCACCTGGCTAAAGC[G/T]CCACCAGCAACACAG	57674
rs771936795	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80392967	AGGGGACTGATTGGT[C/T]CCCTTATGTTATATG	57674
rs771937435	snp	A/G	1.64762e-05	0.00287016	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358390	GTTACTGACCAGGCC[A/G]GATACTCCGCCCTGG	57674
rs771947392	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384042	AGACTATTCCAGTGC[C/T]TTGGTTTTGAATAGG	57674
rs771947537	snp	C/T	0.000108569	0.00736699	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371864	AGGAATAATATTTCT[C/T]TTTCTGCAGCTTTCA	57674
rs771952527	snp	C/T	6.58924e-05	0.0057395	synonymous-codon	RNF213	GRCh38.p7	17:80309132	GCCAGCCTTATCTGC[C/T]GAGATTGTCTGCAGA	57674
rs771972724	snp	A/T	1.70177e-05	0.00291694	missense	RNF213	GRCh38.p7	17:80289761	AAGCCAGAGGGGAAG[A/T]ACAGAAGTGCAGCTG	57674
rs771992419	snp	C/T	3.30491e-05	0.00406491	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319453	GGCACCCTCCTCCCT[C/T]GCCAAGGGCAATGGC	57674
rs772006141	snp	C/T	3.30082e-05	0.00406239	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389317	ATGCAGCTGAATGTG[C/T]ATACTCAAGACATCC	57674
rs772019621	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378796	GGTGTGTTATCAGCC[A/G]TGACTCTCAGTATAT	57674
rs772027550	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367499	ATCTTAGTGAGAGCG[A/G]AGGAGACCTTAAAAG	57674
rs772035323	snp	C/T	3.53232e-05	0.00420242	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386856	CGGCAGATCGTCAGC[C/T]GCTTCCTCCAGGGCA	57674
rs772075460	snp	C/T	1.68394e-05	0.00290162	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354003	AAACGGATGACCCAA[C/T]CGTCTCCACCAACAG	57674
rs772077194	in-del	-/C	0.000188541	0.00970748	intron-variant	RNF213	GRCh38.p7	17:80317322	GGGCGTGAAGGCAAG[-/C]TGGAGAACCCCAGAC	57674
rs772088606	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80339833	GGAGCGTTGTCTCCC[A/G]AGAGGTCTGCAGGTC	57674
rs772098318	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80331098	TGCTGGGATTACGGG[C/T]GTGAGCCACTGTGCC	57674
rs772101669	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80272423	GGCAGAGTAGGCCGA[-/C]GGGGATGCTGACAGC	57674
rs772105432	snp	A/G	8.25062e-05	0.00642233	missense	RNF213	GRCh38.p7	17:80343185	AAGATGCAGTTAAAC[A/G]TGAAAAATGTGCCTC	57674
rs772117564	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376400	GACAATTCTGTGCCA[C/T]TGTTGAGGGCGGGGC	57674
rs772121856	snp	A/C/G	3.29474e-05	0.00405867	missense	RNF213	GRCh38.p7	17:80345581	CGGTGTGGGATCCCG[A/C/G]TTATCATCATGGGAG	57674
rs772124667	in-del	-/AGAG			intron-variant	RNF213	GRCh38.p7	17:80276609	GAGATCCTTCCTCAA[-/AGAG]AGAGAGAGAGAAGGA	57674
rs772125121	snp	C/T	1.65299e-05	0.00287483	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367745	GTCCCTGCCTTTCTT[C/T]AGTGTCTTCGAGAGA	57674
rs772130638	in-del	-/T	1.64775e-05	0.00287027	frameshift-variant	RNF213	GRCh38.p7	17:80306415	ATATCCTGGACTGTC[-/T]TTTCAGGGATTTACT	57674
rs772152306	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80316508	TGATAAGTAAGTACA[C/G]CGTGTGTCCCAGGAG	57674
rs772171379	snp	C/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320428	TGCGATCCTGGCTCA[C/T]CGCAACCGCTGCCTC	57674
rs772180083	snp	C/T	3.30923e-05	0.00406756	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364595	ATGCACGGATCCACC[C/T]TTTTCCGAAAGGAAG	57674
rs772188461	snp	C/T	1.66142e-05	0.00288216	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319516	GTGCTGCACAGTCCC[C/T]GCTGCTCGCACCATC	57674
rs772197179	snp	A/C	3.29451e-05	0.00405851	synonymous-codon	RNF213	GRCh38.p7	17:80345172	GGGGAAGCACATGGT[A/C]ACCATGGATGGGGTT	57674
rs772205057	in-del	-/T	3.33383e-05	0.00408265	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393312	CCATGCTGAGGAGAC[-/T]TGTTTTAAATGCTCT	57674
rs772205787	snp	C/T	1.65244e-05	0.00287436	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358285	CTCTCTTCTGTGCTG[C/T]AGGCACACCCTCTGG	57674
rs772226803	snp	C/T	3.29745e-05	0.00406031	intron-variant	RNF213	GRCh38.p7	17:80309204	ACAAGGTATCACACC[C/T]GGGATAGGTGCGGAA	57674
rs772239406	snp	A/C	1.66217e-05	0.0028828	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288002	GCCAGCCGAGCCAGC[A/C]CCCAGGCACAGCCAC	57674
rs772241954	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80312880	GCTTCTGCCAAGGCC[C/T]GTGGTCCCTCCATCG	57674
rs772246712	snp	A/G	3.29815e-05	0.00406075	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369494	TCTTCTGTTTCTCGT[A/G]TTCTAAGGGAAGCCA	57674
rs772250172	snp	A/G	1.73159e-05	0.00294239	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288382	AGTCATCCGGGAGAG[A/G]TGGCCTGGGAGTGGC	57674
rs772252232	snp	A/G	1.64912e-05	0.00287147	missense	RNF213	GRCh38.p7	17:80291789	GCGAGTACGTCAACC[A/G]CTGTCTGTTCATAAA	57674
rs772255656	in-del	-/AGC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355460	GCTCACGGAGGAAGA[-/AGC]GGGGTGACCGGGAAT	57674
rs772257532	snp	A/G			synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377790	CCATCCTTGCTCCGT[A/G]GGAGAGGTGAGTCTT	57674
rs772276088	multinucleotide-polymorphism	CA/TT			intron-variant	RNF213	GRCh38.p7	17:80269412	GTCCTATCATCTATC[CA/TT]TCCATCCATCCATTC	57674
rs772280055	snp	A/C	1.6498e-05	0.00287206	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386416	CGTGGAAAAACTCTC[A/C]AAGGAAAACAACAGG	57674
rs772291975	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360983	TTAGGGGCTGCACCC[C/T]GCCCACTAGAAGCCA	57674
rs772316376	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80334397	AAAGGGCAGAAAGAC[A/G]TTGCCTGCATGCTTT	57674
rs772316629	in-del	-/TTAC			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367466	AGATGGTCATTATTA[-/TTAC]TTAAAGTTTGAAATA	57674
rs772323205	snp	A/G	1.64887e-05	0.00287125	missense	RNF213	GRCh38.p7	17:80347553	TTATTTTTGGTTCTG[A/G]TTTCCCCAAGGACCA	57674
rs772332535	snp	A/C	1.64898e-05	0.00287135	intron-variant	RNF213	GRCh38.p7	17:80319164	CATCCGAAAGCTCTG[A/C]AACCACCCCCCTTTG	57674
rs772338144	snp	A/C	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80291686	ATTTCCAAGAAGCAC[A/C]TAGATAAATACATTC	57674
rs772347231	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382346	ATTTTCTTTTGCTAA[A/T]CTGCAAAAATCACAA	57674
rs772347667	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386899	GCCTCAAGGTAGGGC[C/T]GACTCCTGCCACTGC	57674
rs772348591	snp	G/T	1.67407e-05	0.00289311	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373087	CAGCAGCCAGCGGGG[G/T]ATGGAGTTCGTGCAG	57674
rs772364250	snp	C/T	1.67016e-05	0.00288973	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383054	AAATCGCAGCTGTGA[C/T]TTCTCCTGAACTGGA	57674
rs772380251	snp	A/T	4.94271e-05	0.00497102	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288635	TGGGGTCTTTCAGGC[A/T]GTTGATGCTGTAGCT	57674
rs772394858	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372245	TGAGTGGGGACATTA[C/T]GGATACTTTTTATCT	57674
rs772405453	snp	C/T	1.69838e-05	0.00291404	missense	RNF213	GRCh38.p7	17:80347193	AGGAATTCTTCGGGC[C/T]TCGTGACTACTACAG	57674
rs772413887	snp	G/T	3.29739e-05	0.00406028	missense	RNF213	GRCh38.p7	17:80346347	TCTCCAAGTCCAGCG[G/T]CAGCAAAAATCACAC	57674
rs772418008	snp	C/T	3.29511e-05	0.00405887	stop-gained	RNF213	GRCh38.p7	17:80344852	TACCAGTATTTAAGA[C/T]GATTCAATCAAAACC	57674
rs772443163	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351381	GCACCGGGGCAGGCC[C/T]ATTGAGGAGCACAAG	57674
rs772445640	snp	A/C	1.9128e-05	0.00309251	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363803	CAGGTGAGACCCAGG[A/C]GCCCTCACCCACTGC	57674
rs772463155	snp	A/G	1.64841e-05	0.00287085	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393401	GTGAAATTCTTCCTG[A/G]AATGGCATCTCAGTT	57674
rs772480294	snp	G/T	1.66106e-05	0.00288184	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353077	GAGTCACGAGGCGGA[G/T]CCCCTGGGGGAGCAG	57674
rs772480406	snp	C/T	3.30327e-05	0.0040639	missense	RNF213	GRCh38.p7	17:80348123	TGCTGAACTGCGCTA[C/T]GCCCGATGCCGTGGT	57674
rs772492254	snp	A/G	0.000114607	0.00756903	missense	RNF213	GRCh38.p7	17:80336370	GACCAGTACCTGCCC[A/G]GGAAACTGGTGAGTC	57674
rs772499270	in-del	-/T			intron-variant	RNF213	GRCh38.p7	17:80309742	TCTCCCATGGATCAG[-/T]TTTTTTTTTTGTTTT	57674
rs772501643	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80293088	TCTGAGACAGGATCT[C/T]GCTCTGTCACCCAAG	57674
rs772519160	snp	C/T	1.64958e-05	0.00287187	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388711	CCGATAAACCTGATC[C/T]TGTGCACGGGGCTTT	57674
rs772520104	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80274007	GAGCTTCTGCCGTGT[A/G]TATCTGTGTCCCAAG	57674
rs772520105	in-del	-/TC	0.375	0.216506	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369788	TGTGAACACACAAAA[-/TC]TCTCTCTCCATTCAA	57674
rs772528455	snp	A/G			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395890	CTTTGTCTGCCCTGC[A/G]CCAGCCTCACCTCAC	57674
rs772532641	snp	C/T	0.000148249	0.00860829	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377834	GGGTTTGAGGGGTGG[C/T]GTGCACTCCTGGGTT	57674
rs772552882	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	RNF213	GRCh38.p7	17:80307148	TCAGGATGTTCAGAA[C/T]GTTCAGAACATTTTA	57674
rs772570067	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382095	ACCATGCTGGGAGCA[C/T]GTGTCGTCCACACAG	57674
rs772576920	snp	A/G	5.00363e-05	0.00500156	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354150	GGGCCTCTTGAATGA[A/G]GATGACGCGTGCCAC	57674
rs772585503	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377744	CATTAGCCAATGTGT[A/G]TCCTGTTCTCTTCAC	57674
rs772629828	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383306	ATTCCTGGGAATCCA[A/G]CAAGTGCAGGCAGTG	57674
rs772641133	snp	C/T	1.66507e-05	0.00288532	missense	RNF213	GRCh38.p7	17:80273331	AAGGGGGCCCGTGCT[C/T]GTTCCCGGGCTCAGA	57674
rs772653818	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372449	CCACAGTCACATTGG[C/T]GACTGTAGAAGCTTG	57674
rs772660885	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385116	GAAGCAGTTCCAGAA[C/T]GTCCAGCAAGTTGAA	57674
rs772675125	snp	C/G	4.94694e-05	0.00497316	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363244	TTTCCAGAATCCTGA[C/G]CATCTACCCTCAGGT	57674
rs772679326	in-del	-/AA	1.90609e-05	0.00308708	splice-acceptor-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372972	TCTCGTTGGCCTCTC[-/AA]AGAGATGGCCAAGGA	57674
rs772692667	snp	C/T	1.69347e-05	0.00290982	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372607	TTTCCTTAAGGCATA[C/T]TCTCCAGCAAGCCGG	57674
rs772698201	snp	A/G	5.0119e-05	0.0050057	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354157	TTGAATGAGGATGAC[A/G]CGTGCCACGGTATGA	57674
rs772699390	snp	A/C	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80290595	CCGGGTGGAGGAGTC[A/C]CCGTGTTCTTCCACG	57674
rs772699789	snp	C/T	3.29544e-05	0.00405908	synonymous-codon, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361780	GCAGACTCCTCTGGG[C/T]AGGTTTCTTGCCCAG	57674
rs772738249	snp	A/C	1.65471e-05	0.00287633	missense	RNF213	GRCh38.p7	17:80343223	AATTCGACTGATCGA[A/C]CCTCAGGTGGATGAG	57674
rs772749848	snp	A/G	0.00025582	0.0113068	missense	RNF213	GRCh38.p7	17:80339906	CCAGCCGCCCTGGCT[A/G]TCTACATGCAAACCC	57674
rs772761775	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329317	ACTAGGTCAGTCGCT[C/T]GGCTAGGTCTAGAAT	57674
rs772765259	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80302884	AACCACAAACTTTCT[C/G]TTTAAGTATAATCTC	57674
rs772768133	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292555	TGACATCCAGAGCCC[C/T]GTCTGCAGGCTCCTG	57674
rs772768933	in-del	-/T	9.88704e-05	0.00703032	intron-variant	RNF213	GRCh38.p7	17:80344657	CTTGTAACCATTTCA[-/T]TTAATGTCTCTCCTT	57674
rs772777062	snp	G/T	4.95103e-05	0.00497521	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389786	ACATGAGTGGGGGTG[G/T]GAGACCTCAGCCCCC	57674
rs772807916	snp	A/C	1.65685e-05	0.00287819	synonymous-codon	RNF213	GRCh38.p7	17:80350337	CAAATGTAAAATCCT[A/C]ATTTTTCAGACAGAT	57674
rs772816999	snp	C/G/T	0.000342811	0.0130885	intron-variant	RNF213	GRCh38.p7	17:80325009	CTTCTAAATGTCCCT[C/G/T]TTTTATTAATTTTCT	57674
rs772858082	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80305328	GGATTACAGGTGTGC[A/G]CCACCACGCCTGGCT	57674
rs772883881	snp	C/T	3.33017e-05	0.00408041	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361698	GCGCCATGACTTAGA[C/T]GCACTCCAGGCCGCT	57674
rs772888681	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382145	CAATCACCATCACAG[C/T]TGTGTGCTGATTTAT	57674
rs772892791	snp	A/C/G	3.29637e-05	0.00405968	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381520	AACCAGATCCCCGCT[A/C/G]AACACTCTGTTCCGT	57674
rs772894037	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80333564	CCGGGTGTGGTGTCA[C/G]GTGCCTGTAATCTCA	57674
rs772907801	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365389	AGCAGCCCAAGGCTA[A/C]GGTACCAGCTCCCCG	57674
rs772925042	snp	C/T	1.66913e-05	0.00288883	synonymous-codon	RNF213	GRCh38.p7	17:80346627	CGAGCTGAAGATTCC[C/T]CTCTTCCTGGTGGGG	57674
rs772938055	snp	A/G	0.00011462	0.00756946	missense	RNF213	GRCh38.p7	17:80339634	AGGCCGCCAGGTACC[A/G]CATGAGGAGAGTCAT	57674
rs772947722	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80307080	AGCAATGACAGTGGC[A/T]TTGTGATTCAATCTT	57674
rs772957648	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80318261	TCCGAAAGAACCAGT[G/T]GGGAGAGAGTAGGCA	57674
rs772974232	snp	C/G	4.94181e-05	0.00497057	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376430	CCTAGTGACAGCAAC[C/G]TTGATGGAACGGTGA	57674
rs772975554	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390700	ACTACACCCAGCCTA[A/G]AAGTCATATATTCTA	57674
rs772981081	snp	C/G	1.64792e-05	0.00287042	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369665	CGCTTAAGAGATGCT[C/G]CCCAGAGTAGGTTGC	57674
rs772984070	in-del	-/C			intron-variant	RNF213	GRCh38.p7	17:80342535	CCTGGGACTTAATTT[-/C]TTCTCTCTCTCTCTC	57674
rs772993276	snp	A/G	3.29614e-05	0.00405951	synonymous-codon	RNF213	GRCh38.p7	17:80345766	CGCCAATAAGGACCA[A/G]CATCAGTTGGACACC	57674
rs772994903	snp	A/G	1.6473e-05	0.00286988	missense	RNF213	GRCh38.p7	17:80345261	CATACGTTTTCTTCA[A/G]TGACGACCACACAAC	57674
rs773004529	snp	A/G	3.29592e-05	0.00405938	missense	RNF213	GRCh38.p7	17:80347708	TACGTCCACCTCGGC[A/G]GCCAGAAGTACGTGG	57674
rs773015380	snp	A/G	4.94173e-05	0.00497053	missense	RNF213	GRCh38.p7	17:80345194	GATGGGGTTAGGGAA[A/G]AAGATCTAGCGCCCT	57674
rs773015439	snp	A/G	1.64749e-05	0.00287005	missense	RNF213	GRCh38.p7	17:80346253	TTTGTCAGCCTCAGG[A/G]ACGTGGAGCGCTGTG	57674
rs773071450	snp	A/T	3.74504e-05	0.0043271	intron-variant	RNF213	GRCh38.p7	17:80350435	GAAACTATGTAAAAA[A/T]CCCAAAACGTAGGAA	57674
rs773074293	snp	C/T	1.64757e-05	0.00287012	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319321	CTGCCAGGTGAACAA[C/T]CTCTCCTCCTGGGAA	57674
rs773077310	in-del	-/GAC			intron-variant	RNF213	GRCh38.p7	17:80315252	GAGGTGATGGTGGTG[-/GAC]GTGATGGTGGAGGTA	57674
rs773083386	snp	A/G	1.65778e-05	0.002879	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358484	AATAATGAAAGGTGA[A/G]TGGAAGGCTTTCTTT	57674
rs773083903	snp	A/G	1.68783e-05	0.00290498	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363345	GCCTGCCCTGAGCAA[A/G]CCTTGTGGTGCTTCC	57674
rs773098626	snp	A/G	1.64753e-05	0.00287008	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383729	TCAGCCAAGATAAGC[A/G]TATCAGCTCTAACCC	57674
rs773104420	in-del	-/TG	1.64732e-05	0.0028699	frameshift-variant	RNF213	GRCh38.p7	17:80349806	CTAACAAGTCACGAC[-/TG]TGAAATTTTAGAATC	57674
rs773107040	snp	A/G	3.31592e-05	0.00407167	missense	RNF213	GRCh38.p7	17:80291825	CACTTCTGGGCTCAG[A/G]AGGTAAGTCGTGGCA	57674
rs773110444	snp	C/T	1.93246e-05	0.00310836	missense	RNF213	GRCh38.p7	17:80343324	TGGACGTGACCTCCT[C/T]AGTAAGTGCCCTCCA	57674
rs773116377	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80264723	AGACAGTCAAACCAC[A/C]GACCCCCTTACAAGA	57674
rs773123588	snp	A/G	1.64735e-05	0.00286993	intron-variant	RNF213	GRCh38.p7	17:80306246	GTCCCTATTTCTCTT[A/G]TGCAGGAGTTCCCTA	57674
rs773124458	snp	G/T	1.6799e-05	0.00289814	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373107	AGTTCGTGCAGGGCC[G/T]CTCCAAGCCCGGCCG	57674
rs773128866	snp	C/T	4.94817e-05	0.00497377	missense	RNF213	GRCh38.p7	17:80313133	ACATGCTCACATCTT[C/T]AGGTGCCTCATTCAC	57674
rs773150853	snp	A/G	0.000114844	0.00757684	intron-variant	RNF213	GRCh38.p7	17:80278720	TGGAGCTGTGCGTGG[A/G]GTGCACAGCCCTGCC	57674
rs773151981	snp	C/T	0.000478449	0.0154595	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386682	AGCGCTGTCTTTCTG[C/T]CCCTCAGCTATTCCG	57674
rs773153584	snp	A/T	1.8255e-05	0.00302112	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383651	ACCTCACTTCCAGAA[A/T]TTTTTTTTTCATTTT	57674
rs773169040	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80269090	AGCATAGGAGGAAGA[A/T]GAAAGCCAGAAGACT	57674
rs773192393	snp	C/T	1.66999e-05	0.00288958	missense	RNF213	GRCh38.p7	17:80346742	AGCCTGAAGCAGGTC[C/T]ACCTGGTGTCCTTCC	57674
rs773192577	snp	A/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80386119	CTATCAGCATATGAG[A/T]TGGGGCAGAACCGAG	57674
rs773203556	snp	A/C/G	3.3099e-05	0.004068	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376521	CCCTAAAGAATCTGG[A/C/G]CTTCTCCCCAGCCAC	57674
rs773211561	snp	A/G	3.37371e-05	0.00410699	intron-variant	RNF213	GRCh38.p7	17:80298544	GAGTTGTGCTTATCT[A/G]CATGAATCTGGGAAG	57674
rs773230795	snp	A/C	0.000157791	0.00888091	intron-variant	RNF213	GRCh38.p7	17:80336528	AAGCTTTTCTTCATA[A/C]ATGGAAATTCACCAT	57674
rs773231879	snp	A/G	3.30316e-05	0.00406383	intron-variant	RNF213	GRCh38.p7	17:80294693	TGATGGTCTTAGGTA[A/G]GCTCTTGTTCCTTCT	57674
rs773255183	snp	A/T	1.64749e-05	0.00287005	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376270	ACAATATTCTTTGAT[A/T]CATCTTAATGTTAAG	57674
rs773284252	snp	A/C	1.65007e-05	0.00287229	missense	RNF213	GRCh38.p7	17:80347445	GAGAGCAGGAAGATG[A/C]TGAGTCCCGCTACTT	57674
rs773284272	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393795	CAACATTGTTTACAT[A/T]CCAGGAGACTTGTAG	57674
rs773293459	snp	A/G	1.64781e-05	0.00287033	missense	RNF213	GRCh38.p7	17:80345909	TTATAGCTGCCTGCA[A/G]TCCATACCGGAAGCA	57674
rs773325407	snp	C/T	1.65045e-05	0.00287263	intron-variant	RNF213	GRCh38.p7	17:80289656	TTTGGTTCCTTGTTC[C/T]AGGAAGCTGAGACCA	57674
rs773336236	in-del	-/CC	1.64792e-05	0.00287042	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379585	TAAAATGGTACTGCT[-/CC]AGAAGTGGTTCTAGT	57674
rs773336941	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381159	CCCTGTGGCGTATGA[C/T]GGTATGGGGGGAACT	57674
rs773342519	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80307246	CTCACATGCGGCCCC[C/T]GGGGGCTTCCTCTGA	57674
rs773352659	in-del	-/AA	1.65444e-05	0.00287609	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383686	ATCCAGCATCTAGAT[-/AA]AACCCTTCCCACCAT	57674
rs773363462	snp	G/T	0.000128682	0.00802026	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389083	CCCCGCATGTGGCTT[G/T]GGCAGTGAAGGGGCT	57674
rs773365216	snp	C/T	1.65127e-05	0.00287334	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393519	TTTCCTCAGCTATCT[C/T]TGGATGACTTTGGAG	57674
rs773373096	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290965	AGGTGTGTACCACCA[C/T]GCCTGGCTAATTTTT	57674
rs773373243	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80279701	CTCGAACTCCTGGCC[C/T]CAAATGATCCACCCA	57674
rs773389034	snp	C/T	1.65414e-05	0.00287583	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369788	TGTGAACACACAAAA[C/T]CTCTCTCTCCATTCA	57674
rs773408143	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80309996	CATGACCTCATGATC[C/T]GCCTGCCTTGGCCTC	57674
rs773411456	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379697	CCACAAACCTCGGGA[C/T]GGCTTTCATCTGGTC	57674
rs773418277	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80334775	GGGACTACAGGCGAC[C/T]GCCACCACGCCCGGC	57674
rs773418570	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80362767	TTCGAAAAATAAGAA[A/T]TAGTTTAATTGTCCG	57674
rs773419598	in-del	-/AAA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375543	CGTGTCTACTAAAAG[-/AAA]AAAAAAAAGAATTAG	57674
rs773427301	snp	C/T	1.64827e-05	0.00287073	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351764	ATCACAAAACTGTCC[C/T]GGGTGGGAAGAGGAA	57674
rs773432664	snp	G/T	1.65078e-05	0.00287291	missense	RNF213	GRCh38.p7	17:80348210	ACTTTCACAGACAGA[G/T]GCACAACTCCTTTGC	57674
rs773440044	snp	A/T	1.64732e-05	0.0028699	missense	RNF213	GRCh38.p7	17:80295783	ATGAGTTTCACCGTG[A/T]CCTAAGCCACATCCT	57674
rs773448503	in-del	-/GAGCCCTCGGCACC	3.46717e-05	0.00416349	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288400	CCTGGGAGTGGCACT[-/GAGCCCTCGGCACC]GAGCCCTCGGCACCT	57674
rs773479376	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395567	GATCTGGGACTGAAA[C/T]GCTTACACCTCTGCC	57674
rs773484495	snp	C/G	3.29701e-05	0.00406005	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354538	GTTGGCAAGGGAAGC[C/G]TGCAACCAGGACGCT	57674
rs773491121	snp	C/T	1.64741e-05	0.00286998	missense	RNF213	GRCh38.p7	17:80344940	GCCTCCAGCATTTCC[C/T]GTTTCACTGCGGGGT	57674
rs773491415	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393177	CTAGAGACAGGGTTT[C/T]GCCATGTTGCCCAGG	57674
rs773494889	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320854	TAGCCAGGCATGGCC[A/G]GGCACACCTGTGGTC	57674
rs773504923	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80290500	ACGTGTGTGTGTGCG[C/T]GTGTGTGCATGCACA	57674
rs773510919	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80298303	TCAGCTCACTGCGGG[A/T]TCTTTATTCCCTTCC	57674
rs773519568	snp	A/G	1.68434e-05	0.00290197	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287788	GTAAATCTAAGAAAT[A/G]AAGTGAGTGTCTCTC	57674
rs773521334	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80300479	CAACTCCTGACCTCA[A/G]GTGATCCACCTGCCT	57674
rs773522414	snp	C/T	1.64757e-05	0.00287012	synonymous-codon	RNF213	GRCh38.p7	17:80345367	GGTCATCAAGAGAGA[C/T]GTCATGACCAGGGAC	57674
rs773524440	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80343812	AGAGTTGGGAGAACT[C/T]GCCATCGTGTCGTGT	57674
rs773529074	snp	C/T	1.68812e-05	0.00290522	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372710	AGAGCTGCAGATTTC[C/T]TCTCGGAGCCTGAGG	57674
rs773533554	in-del	-/AGA	1.64794e-05	0.00287044	cds-indel, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353626	AAACAGAAAGTTCTG[-/AGA]AGGTGGGAAAGGAAA	57674
rs773534519	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375429	GGCAGGCAGCGGTGC[A/G]GGGGCGTCTATCCTA	57674
rs773550228	snp	A/G	1.66189e-05	0.00288256	synonymous-codon	RNF213	GRCh38.p7	17:80347344	CTTTCTGGCCAATTT[A/G]CCCGAGGCCAAGTGC	57674
rs773557485	snp	G/T	0.000307209	0.0123899	missense	RNF213	GRCh38.p7	17:80340288	TCCCGAAGCAGACCC[G/T]GTCGGCGGCAGCCGT	57674
rs773563807	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369989	CTTGGGGAGCTTTTT[C/T]GGTGAGACACAGCCT	57674
rs773567458	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359136	CCCCCACCCCCTTCC[A/G]CAGGCCTGATGATGT	57674
rs773575910	snp	C/T	1.66192e-05	0.00288259	synonymous-codon	RNF213	GRCh38.p7	17:80340160	CGTCATGGTCTGTGA[C/T]GGGGACTGGGAGCAC	57674
rs773587636	snp	G/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377506	CTCCAAAAGTACCCC[G/T]GGTATGGGCCTATAT	57674
rs773609720	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80301384	CAGAGTGAAGAGACA[G/T]TCCACGGAATGGGAG	57674
rs773614989	snp	C/G	2.07016e-05	0.0032172	intron-variant	RNF213	GRCh38.p7	17:80317171	GAGTGGGTGTGACCT[C/G]TGTGCGGGTTTTGCA	57674
rs773619642	snp	C/T			intron-variant, missense	RNF213	GRCh38.p7	17:80288887	CAAAGCTCTGGCCTT[C/T]GGGGTGCTCACATTC	57674
rs773631138	snp	A/C			missense	RNF213	GRCh38.p7	17:80263720	TGTCTCCAAGGAGGA[A/C]ACCCCCAAGTTCTGC	57674
rs773634303	snp	G/T	1.64808e-05	0.00287057	missense	RNF213	GRCh38.p7	17:80290697	GGGGAGTCAAAATGG[G/T]ACAGCAATATCTGTG	57674
rs773639847	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80284818	TCAGGGGACAAGACA[C/G]CGCCTCCTCTGGTGA	57674
rs773658405	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380460	GAGATGAGAACAATA[C/T]GGACACCCATGGGAT	57674
rs773660157	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388053	CAAGCTCCACCTCCC[A/G]GGTTCACTCATGCCA	57674
rs773668463	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363171	GCGCCCGAGGAAGAG[A/G]TTTCCTTACCGTGGG	57674
rs773689367	snp	A/C	1.671e-05	0.00289045	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386235	TCTGCTTAAGCATAA[A/C]CCTGTCGTTTAAAGG	57674
rs773692675	snp	C/T	6.59294e-05	0.00574111	synonymous-codon	RNF213	GRCh38.p7	17:80346319	ATGCTCTTAGCGCAG[C/T]TGAATGCCTTTCTCT	57674
rs773699555	snp	C/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354666	CTCCATCCGGGCCAT[C/G]GGGACTGAGCTGTTT	57674
rs773700733	snp	C/T	1.69971e-05	0.00291518	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288180	CCAGGACGCTTCCAT[C/T]CCCTCTGGGGGCAGA	57674
rs773701444	snp	C/T	3.62516e-05	0.00425729	missense	RNF213	GRCh38.p7	17:80317243	ATGGCTGGAAGGAGT[C/T]GTTGCTGGGAGACAT	57674
rs773703374	snp	A/C	1.66668e-05	0.00288672	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363653	CACGGAGATGCTGAC[A/C]AGAAACACCCTGAAG	57674
rs773708335	snp	C/T	4.94197e-05	0.00497066	synonymous-codon	RNF213	GRCh38.p7	17:80343961	CTGCCATTTGTATAT[C/T]GTTGAAATCCTGGAA	57674
rs773716303	snp	C/T	1.81069e-05	0.00300884	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376871	GCTGTCTCTGTCTTC[C/T]TGTTTTTCAGCATGC	57674
rs773721359	snp	A/G			missense	RNF213	GRCh38.p7	17:80290664	CATAAAGTCTTCATC[A/G]GAGGAGGAGAAGAAT	57674
rs773722437	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272633	TCCCAGCACTGGCAT[A/G]CTGGGGATCAACATG	57674
rs773749814	snp	A/C	7.71129e-05	0.00620891	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372939	TAAATGCCCTAAGTC[A/C]CCAGCCACTCACCCG	57674
rs773779469	snp	A/C	2.14365e-05	0.0032738	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381757	AAGGGCTGGGCGGGG[A/C]TCACACAGCACAACG	57674
rs773785078	snp	C/G	3.35655e-05	0.00409654	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372694	CCGCCTCTGCCTCGA[C/G]AGAGCTGCAGATTTC	57674
rs773799645	in-del	-/TT	0.000200894	0.0100203	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360034	GTCTCACAAACCCTC[-/TT]CTTATCATCCCTCAC	57674
rs773801468	snp	A/G	4.94336e-05	0.00497135	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381534	TGAACACTCTGTTCC[A/G]TTGCCCCCACAGGCT	57674
rs773805669	snp	C/G	1.64751e-05	0.00287007	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390077	AAATGCTAAGCTCCT[C/G]AGCACATTCCTAAAT	57674
rs773809586	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80306261	ATGCAGGAGTTCCCT[A/G]CTTCAGTTTATGAGA	57674
rs773810979	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80272556	CCCATGACCGCAAAC[G/T]GCACCAAGCCATTCG	57674
rs773812976	snp	A/G	3.38834e-05	0.00411589	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288235	CCCCCCACCTCTGCT[A/G]GTGAAGGCCATTCTA	57674
rs773834081	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80285730	GGCTGGAGTGCAGTT[A/G]CGTAATATCGGCTGA	57674
rs773851241	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367988	GCCGTGCTCCATCTG[C/T]CTGGGAGATGCAAAG	57674
rs773851265	snp	A/G	1.69645e-05	0.00291238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363362	CTTGTGGTGCTTCCA[A/G]CTCCACTCTGGGAAT	57674
rs773870708	in-del	-/AATTTTGGAGTTTTTAGTTTTCA			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360304	TAGAATTGCAAGGTG[-/AATTTTGGAGTTTTTAGTTTTCA]CACTTTGTTTGTGCA	57674
rs773878812	snp	C/T	3.32198e-05	0.00407539	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376539	TCTCCCCAGCCACCA[C/T]GGCGGTAAGAGTAGG	57674
rs773882351	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326928	TAATATTACTGGGAG[A/G]GAAATCCTAAGTGGT	57674
rs773887136	snp	A/G	3.29473e-05	0.00405864	missense	RNF213	GRCh38.p7	17:80345339	TCGATGCCATCAGTC[A/G]CTTGACTGGGAAGGT	57674
rs773894254	snp	A/T	0.000117931	0.00767801	missense	RNF213	GRCh38.p7	17:80328338	TCCAGGGGAAAAAAG[A/T]CTTTCACCCCAGGAT	57674
rs773896013	snp	A/G	1.65034e-05	0.00287253	missense	RNF213	GRCh38.p7	17:80313078	TTCCAAGGGACCCTT[A/G]CTGCTACGAAAAGGT	57674
rs773896295	snp	C/T	1.6473e-05	0.00286988	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80367872	TTAGGTTTGGATCTG[C/T]GAAGGCGAGAATTCT	57674
rs773897587	snp	A/G	4.70832e-05	0.00485174	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288064	CCCACCGAGGTTGGC[A/G]ACAGCCCCCTGCAGG	57674
rs773916131	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RNF213	GRCh38.p7	17:80290600	TGGAGGAGTCACCGT[A/G]TTCTTCCACGCCATC	57674
rs773925198	snp	C/T	1.65184e-05	0.00287384	synonymous-codon	RNF213	GRCh38.p7	17:80347950	TGTCAAAGCACATCA[C/T]TTCCAGAAGAGGCAC	57674
rs773930893	in-del	-/C	1.78442e-05	0.00298694	intron-variant	RNF213	GRCh38.p7	17:80349942	TGCTGCCCTCTCCCT[-/C]CCCAGCCGCAGCCGT	57674
rs773931178	snp	A/G/T	0.000152113	0.00871994	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363599	CACGCCCTGCTGTCC[A/G/T]TCTCCCCAGACCCTG	57674
rs773939686	snp	C/T	8.23621e-05	0.00641672	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389906	TCTGAACAGCTGCTG[C/T]GGCTGCACAAAGTAA	57674
rs773954576	snp	A/G	1.65029e-05	0.00287248	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386795	CCAGTACCAGGTGGA[A/G]GAGGGCAGAGAGACC	57674
rs773970330	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80326146	TAATTTTAAAACAAG[C/G]TCTTCTCTGTTGCGC	57674
rs773991295	snp	A/C	1.67576e-05	0.00289457	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360030	TGACGTCTCACAAAC[A/C]CTCTTCTTATCATCC	57674
rs773996734	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80293684	AAAAAATTGGCCGGG[C/T]GTCTTGGCAGCGGGC	57674
rs774018198	in-del	-/C	1.65015e-05	0.00287237	frameshift-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352993	CCACCCTCATGGTTT[-/C]CTGATGTGACCAGGC	57674
rs774027708	snp	A/C/G	1.67744e-05	0.00289602	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372692	ATCCGCCTCTGCCTC[A/C/G]ACAGAGCTGCAGATT	57674
rs774043466	in-del	-/CGG			upstream-variant-2KB	RNF213	GRCh38.p7	17:80260515	ACGCCTGCGCGGGGC[-/CGG]CGGCGGCGGCGGGCA	57674
rs774043685	snp	A/G	1.64974e-05	0.00287201	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386697	CCCCTCAGCTATTCC[A/G]TGGATGCCGCCGAGG	57674
rs774063002	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357217	ACCGTGCCCAGCCAC[C/G]TTTTAATTCTTATCC	57674
rs774063932	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80336422	TTTTGTTGAATAGAG[C/T]ATTGCTTAGCAACGT	57674
rs774067349	in-del	-/A			intron-variant	RNF213	GRCh38.p7	17:80300504	CTGCCTCGGCCTCCC[-/A]AAGTTCTAGGATTGC	57674
rs774079214	snp	C/T	1.64966e-05	0.00287194	intron-variant	RNF213	GRCh38.p7	17:80294713	TTGTTCCTTCTGTCC[C/T]TCTTAGACTGGCATC	57674
rs774096280	snp	C/T	1.65217e-05	0.00287412	missense	RNF213	GRCh38.p7	17:80346851	TGCAGCAGTACGTCT[C/T]TGTGGTGGTGTTAGA	57674
rs774099533	snp	C/T	1.65222e-05	0.00287417	intron-variant, synonymous-codon	RNF213	GRCh38.p7	17:80319450	GTGGGCACCCTCCTC[C/T]CTCGCCAAGGGCAAT	57674
rs774102851	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80265020	CCTTCAAGGGTGTGA[A/G]CCCCAGTCCTTCCAT	57674
rs774114338	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319929	GTCCAGAAACATTGA[A/G]GTCATTGAATTCCGG	57674
rs774133769	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383761	GTGGCCAAAATAATA[C/T]ATGGTGACCCAGTGA	57674
rs774141676	snp	G/T	1.64732e-05	0.0028699	intron-variant	RNF213	GRCh38.p7	17:80343825	CTCGCCATCGTGTCG[G/T]GTGTTTACACCTCGT	57674
rs774152938	snp	A/G	3.29478e-05	0.00405867	missense	RNF213	GRCh38.p7	17:80344946	AGCATTTCCTGTTTC[A/G]CTGCGGGGTAATAAA	57674
rs774155915	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80268012	TTTATTAGAGATAGG[G/T]TTTCTCCATATTAGC	57674
rs774157175	snp	C/T	1.65042e-05	0.0028726	missense	RNF213	GRCh38.p7	17:80263722	TCTCCAAGGAGGAAA[C/T]CCCCAAGTTCTGCAG	57674
rs774183304	in-del	-/C	1.65318e-05	0.002875	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383955	TTACTGTGGCTCCCT[-/C]CCTCTTTCGGTGCAG	57674
rs774188727	snp	C/T	1.64727e-05	0.00286986	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389962	CAGAGGGACTGCGCT[C/T]CCTTCTCCCTGCAGG	57674
rs774195648	snp	C/T	1.6557e-05	0.00287719	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393541	ACTTTGGAGAGAAGA[C/T]TCCTCTCTCCTCGTC	57674
rs774206865	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383409	CATTAAAAATGAACT[A/G]ACAATCATAGATTAA	57674
rs774221634	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353654	GGAAACCTCTGAACT[C/T]GGAGGCAGTGATGTA	57674
rs774251380	in-del	-/CTAT			intron-variant	RNF213	GRCh38.p7	17:80269595	ATCTATCCGTCCATC[-/CTAT]CTATCTGTTTATCTA	57674
rs774254067	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80324837	TGCTGGACACTTAAG[A/G]AGGCAGTATACAAGG	57674
rs774262157	snp	A/G	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80306361	CACCTGGTTATGTAT[A/G]TGGAAAACTTCATTG	57674
rs774264875	snp	A/T	0.0001155	0.00759847	intron-variant	RNF213	GRCh38.p7	17:80289614	AAAAAAAAAAGAAAA[A/T]GTGGAGGCCGGCCTT	57674
rs774271519	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80395809	AAAGGTTCTTCCAGG[C/T]GAGAAACCTGTGGTC	57674
rs774284591	in-del	-/CAGCCT	1.65201e-05	0.00287398	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380791	GCGTGCCAAAGCGGC[-/CAGCCT]CAGCCTCTGTCTTGT	57674
rs774290815	snp	C/G	1.64749e-05	0.00287005	intron-variant	RNF213	GRCh38.p7	17:80309015	TAACTCTTTGCGGGG[C/G]AGGATTCCCGAGGAG	57674
rs774291021	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277105	AAAGAATACGATATG[A/G]ATCTGTGCTGTAGCC	57674
rs774291168	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391634	TTCATCTTCTCTGCC[A/G]TGTGCCACAGTGCTC	57674
rs774291889	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80338906	TGAGCCGAGATCACA[C/T]CACTGCACTCCAGCC	57674
rs774300433	snp	A/G	1.65444e-05	0.00287609	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80379745	TTCTATTTCCTAAGT[A/G]CTCAAACTTTGGGGT	57674
rs774320609	snp	A/G	3.30104e-05	0.00406252	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361919	CTGGCTAAGGGTCAG[A/G]TGTAGAGCTTGCATG	57674
rs774323897	snp	C/T	3.29614e-05	0.00405951	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369677	GCTGCCCAGAGTAGG[C/T]TGCTTTCTTCCTGTA	57674
rs774326122	snp	A/C	1.64768e-05	0.00287021	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374451	CCAACTAACCTCTGT[A/C]TTCCAGGGGCTGCGG	57674
rs774344687	snp	A/G	8.5097e-05	0.00652236	synonymous-codon	RNF213	GRCh38.p7	17:80340295	GCAGACCCTGTCGGC[A/G]GCAGCCGTGTTCAAT	57674
rs774344890	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80338234	GCAGTCCCTCCTTAC[A/G]ATCCGTAGGATGAAC	57674
rs774359641	snp	C/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377768	TCTTCACAGCTTGTC[C/G]CAACGGCCATCCTTG	57674
rs774360243	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80328727	AGCATGAGCTGCTGA[C/T]GCCCGCTGCAGAAGA	57674
rs774363919	snp	C/T	0.000230608	0.0107355	synonymous-codon	RNF213	GRCh38.p7	17:80345058	TCCGAGTTTTATTGG[C/T]GACACACTGAGGGGC	57674
rs774365380	snp	A/G	0.000131778	0.00811614	missense	RNF213	GRCh38.p7	17:80309112	CTACTTAAGTTTTAC[A/G]AGCTGCCAGCCTTAT	57674
rs774371656	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80311348	TGTCAGGCTCCGGAG[A/G]TCTGTGCAGCCTCTG	57674
rs774378749	snp	C/T	1.64868e-05	0.00287109	intron-variant, missense	RNF213	GRCh38.p7	17:80319391	CTAAGGGCTATGAAG[C/T]ACCCGCTGGGTCTCA	57674
rs774381115	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390883	GCCTGGCCAACTGGT[C/G]AAACTCTGTTTCTAC	57674
rs774386205	snp	A/G	3.29951e-05	0.00406159	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354551	GCCTGCAACCAGGAC[A/G]CTCTCCAGGAGGCGG	57674
rs774386582	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80298582	CCTACATTGTGCACC[C/T]GGAGTCCCGGTGGGC	57674
rs774391200	snp	A/T	1.64885e-05	0.00287123	missense	RNF213	GRCh38.p7	17:80289681	AGACCAAGACCAAGG[A/T]CGAGATGGCTGCTGC	57674
rs774394726	snp	C/T	1.68519e-05	0.0029027	missense	RNF213	GRCh38.p7	17:80298325	TTCCCTTCCAGCTGG[C/T]GGCTGTACCTGGTGA	57674
rs774410143	snp	A/T	1.66183e-05	0.00288251	missense	RNF213	GRCh38.p7	17:80346511	CTTCTGGATGAAATA[A/T]CACGGGCACAGGATC	57674
rs774416027	snp	C/T	3.29473e-05	0.00405864	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389208	CATTAGTGCCATCAG[C/T]GGACAGCTGCAGTCC	57674
rs774433600	snp	C/T	1.64912e-05	0.00287147	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389303	GTGGGGATCCAAACA[C/T]GCAGCTGAATGTGTA	57674
rs774454468	snp	A/G	1.65337e-05	0.00287517	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363134	GTGGTCCTGCACTAG[A/G]AAACTGAAAGCGGCG	57674
rs774463073	snp	G/T	0.000232396	0.010777	intron-variant	RNF213	GRCh38.p7	17:80338031	AGTGGCGCTAAGCTG[G/T]TGGTGTCATCTCGTC	57674
rs774469124	snp	C/T			intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80286979	CTGCTACTCATTTTT[C/T]AGTCTCATCCTTCTC	57674
rs774488037	in-del	-/C			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360930	TTTCTCAGGACAATA[-/C]CCCCAACTGACCCTG	57674
rs774495559	snp	C/T	1.65957e-05	0.00288055	intron-variant	RNF213	GRCh38.p7	17:80348327	CTATCCCCTGTCACC[C/T]AAGAGTCCTAAATCC	57674
rs774502050	snp	C/T	1.72522e-05	0.00293697	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80385638	TTAGTATCCTGTCCC[C/T]TGTACCACTAAGCGT	57674
rs774507957	snp	A/G	3.30006e-05	0.00406192	missense	RNF213	GRCh38.p7	17:80347454	AAGATGCTGAGTCCC[A/G]CTACTTACTCGTGCT	57674
rs774515312	snp	C/T	1.65179e-05	0.00287379	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364581	GCTGGCCTCAGCACA[C/T]GCACGGATCCACCCT	57674
rs774525173	snp	A/G	6.11178e-05	0.00552767	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386878	TCCAGGGCAAGCCCC[A/G]GCTGAGCCTCAAGGT	57674
rs774529826	snp	G/T	1.65386e-05	0.00287559	missense	RNF213	GRCh38.p7	17:80348020	GACGCCTGCGCGTCT[G/T]TGGTGCTGCAGGTCA	57674
rs774567724	snp	A/G/T	3.29453e-05	0.00405854	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376338	TCATTGGCGAATGCA[A/G/T]GATCCTTTCACCTCC	57674
rs774585544	snp	A/G	8.23649e-05	0.00641683	missense	RNF213	GRCh38.p7	17:80349803	CTGCTAACAAGTCAC[A/G]ACTGTGAAATTTTAG	57674
rs774588883	snp	A/C/T	4.95138e-05	0.00497543	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368137	CAGCTGTTTCCCAAG[A/C/T]GCACAGGTACAACAC	57674
rs774601132	snp	A/G	4.94939e-05	0.00497439	synonymous-codon	RNF213	GRCh38.p7	17:80345511	CGACCCCGACAAAAC[A/G]TATGAGCTCACAACC	57674
rs774623823	snp	C/T	1.64947e-05	0.00287177	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369491	CTGTCTTCTGTTTCT[C/T]GTGTTCTAAGGGAAG	57674
rs774625268	in-del	-/T	1.64836e-05	0.0028708	intron-variant	RNF213	GRCh38.p7	17:80306222	ATCTCACTGCGTCTC[-/T]TTTTCTCCGTCCCTA	57674
rs774639080	snp	C/G	9.92441e-05	0.00704359	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390147	ATGATAATCTTGAAA[C/G]TAAAGAACCCCCAAA	57674
rs774660699	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80305431	GATCTGCCTGCCTCG[G/T]CCTCCCAAAGTGCTG	57674
rs774665383	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80291919	CTGGAGAGCACAGAC[A/T]TTGCCTGGGCAGTGA	57674
rs774683327	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80263872	AACCCTGGGCAGCAG[A/G]CAGCTCAGGTGGGGC	57674
rs774691223	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369136	AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	57674
rs774694349	snp	A/G			missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363307	ATGAGCTGGCTGGAT[A/G]TGAGATGGTATGGCC	57674
rs774700048	snp	A/C			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360811	CAATAGTCTTTTCCA[A/C]GTTTACTTATCGTAC	57674
rs774702371	snp	C/T	1.65121e-05	0.00287329	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352894	AGGGCTGAGCAGCAG[C/T]CGGGAAAGACACAAA	57674
rs774716623	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80293479	ATTCTATATATATAA[A/G]TATGGAATTCCTGCT	57674
rs774726359	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80344015	GAGCTCTTCAGCGCT[A/G]GTCTGTACTGTGGGG	57674
rs774744672	snp	C/G	1.71652e-05	0.00292955	intron-variant	RNF213	GRCh38.p7	17:80306477	TACGCAGGTTTGTGT[C/G]TGAAGTCGGCTCTGG	57674
rs774747277	snp	C/G	1.6566e-05	0.00287797	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386287	CTACTGCAGCACTGA[C/G]TTGGATCTGGACACT	57674
rs774775562	snp	A/T	1.64885e-05	0.00287123	missense	RNF213	GRCh38.p7	17:80347541	AGCAGCCGGAGATTA[A/T]TTTTGGTTCTGGTTT	57674
rs774782676	snp	C/T	1.69447e-05	0.00291068	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288249	TGGTGAAGGCCATTC[C/T]AGGACTGAAGATGCT	57674
rs774787395	snp	C/T	1.67936e-05	0.00289767	missense	RNF213	GRCh38.p7	17:80347016	TTGACCCTGCCAAGA[C/T]GAACCGGGGCATTTT	57674
rs774790232	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360266	CAAAGGGATTGCCTG[A/T]CAGTGAAAAGCAGAT	57674
rs774793193	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80264924	CTTTGCACCACCCTT[A/C]CCCAGAGGGCGGCCT	57674
rs774803340	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80370155	TCAAGAGGCCAGAAT[C/T]TGTGGTGCTGAGCCT	57674
rs774822007	snp	C/G			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354306	ACAGTGGGAATCTAA[C/G]AGCATCTCTCAGATT	57674
rs774827247	snp	C/T	0.000362367	0.0134556	missense	RNF213	GRCh38.p7	17:80344684	CCTTTCCAGCGTACA[C/T]GTGTACCCCAGTTCA	57674
rs774834501	in-del	-/TCCA			intron-variant	RNF213	GRCh38.p7	17:80268613	CCATCTGTTTGTCCA[-/TCCA]TCCATCCATCCATCC	57674
rs774841594	snp	C/T	1.65422e-05	0.0028759	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374574	CAAGCCACTGGGCAT[C/T]AAGACTGCTCTGAAG	57674
rs774845683	snp	C/T	1.66328e-05	0.00288377	intron-variant	RNF213	GRCh38.p7	17:80344046	CGTTTTCGCCTGGCG[C/T]GGGGGGCTCTTGGGT	57674
rs774855345	snp	C/G	1.70551e-05	0.00292015	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363747	TCCGATGAGCACATG[C/G]AAGGCAGCGGGAGCC	57674
rs774870039	snp	A/G	1.67601e-05	0.00289478	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390217	GATTTGCACACCTAT[A/G]GGGCGGGGCAGACAC	57674
rs774887509	snp	C/T	1.64874e-05	0.00287113	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368104	ACTGTTTAACTGCCT[C/T]GCCAGACGAATTCTC	57674
rs774895035	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381303	AGGGAAGAAAGAGCA[C/T]ACTGCATAACCAAGA	57674
rs774897347	snp	A/C	1.65463e-05	0.00287626	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385007	TTTTTAGGTAAATAA[A/C]AATTGTTACTGGGTG	57674
rs774898311	snp	C/T	1.81394e-05	0.00301154	synonymous-codon	RNF213	GRCh38.p7	17:80317248	TGGAAGGAGTCGTTG[C/T]TGGGAGACATGGAAT	57674
rs774912407	in-del	-/CA	1.69752e-05	0.0029133	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363366	TGGTGCTTCCAACTC[-/CA]CTCTGGGAATGGAGA	57674
rs774923802	snp	A/G	4.94173e-05	0.00497053	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377738	AAACCTCATTAGCCA[A/G]TGTGTGTCCTGTTCT	57674
rs774928877	in-del	-/CTC	3.29527e-05	0.00405898	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369629	GAGAGCCTGCTCTCT[-/CTC]CTCTTCGTCCAAAAG	57674
rs774937000	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	RNF213	GRCh38.p7	17:80307139	TTAGGATGTTCAGGA[C/T]GTTCAGAACGTTCAG	57674
rs774937118	snp	A/C	1.87145e-05	0.00305891	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363798	GAAGTCAGGTGAGAC[A/C]CAGGAGCCCTCACCC	57674
rs774940630	snp	C/T			synonymous-codon	RNF213	GRCh38.p7	17:80325086	GCGGAAATTTGGCAT[C/T]GTCTTGTCTGCTGTG	57674
rs774943372	snp	C/G	3.48262e-05	0.00417276	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360164	ATCAAGGACTATCTG[C/G]AGGAGCTGTGGGTCC	57674
rs774949775	snp	A/G	1.67784e-05	0.00289636	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358505	GGCTTTCTTTCCCTG[A/G]GGAGAGAAACTATCA	57674
rs774979776	snp	C/G	1.64757e-05	0.00287012	missense	RNF213	GRCh38.p7	17:80345942	CTGAGGAGATGATCT[C/G]CCGTTTGGAGTCAGC	57674
rs775006151	snp	C/T	1.64735e-05	0.00286993	missense	RNF213	GRCh38.p7	17:80343938	GGGAAAATGTGGCTT[C/T]GGAACCCCTGCCATT	57674
rs775020431	snp	C/G	1.64795e-05	0.00287045	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374475	GCTGCGGCAGGACCA[C/G]CCAGGCCAGATGGAT	57674
rs775021098	snp	C/G	4.94735e-05	0.00497336	intron-variant	RNF213	GRCh38.p7	17:80319159	CGCTGCATCCGAAAG[C/G]TCTGAAACCACCCCC	57674
rs775031639	in-del	-/C	4.22003e-05	0.0045933	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353471	CCAGTCCCTGTGCCA[-/C]CTTCTGAGTGGTAAC	57674
rs775062705	snp	C/T	4.95708e-05	0.00497825	synonymous-codon	RNF213	GRCh38.p7	17:80263744	GTTCTGCAGCCAGTG[C/T]GGAGAGAGGCTGCCT	57674
rs775082457	snp	C/T	1.64969e-05	0.00287196	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386705	CTATTCCGTGGATGC[C/T]GCCGAGGTCACTGAA	57674
rs775082582	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361943	TTGCATGATGGGGAC[C/T]GGATGCAGACACGGA	57674
rs775085564	snp	C/T	0.000117587	0.00766678	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363610	GTCCGTCTCCCCAGA[C/T]CCTGGACGCATTTGC	57674
rs775086529	snp	C/T	1.64746e-05	0.00287002	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390067	TGAGCCCGGAAAATG[C/T]TAAGCTCCTCAGCAC	57674
rs775108381	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80336609	TAAGGTGCAAAACAC[A/C]CGTGGAAAAAAGACA	57674
rs775112910	snp	C/G			stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372550	GAAGACCAGTGCTTA[C/G]TCCAGAAATGATGAA	57674
rs775119801	in-del	-/TAGAGT	1.64761e-05	0.00287015	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80358371	ACAGAGACGGCAACC[-/TAGAGT]TACTGACCAGGCCAG	57674
rs775124939	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80308417	CCTGAGTCCCCTCCT[C/G]AGTCCCTCCCAAGGC	57674
rs775147541	snp	A/G	3.29772e-05	0.00406048	missense, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80351740	GAGGACCGTATCTTC[A/G]TCTATTTCATCACAA	57674
rs775149654	snp	A/G	3.29853e-05	0.00406098	synonymous-codon	RNF213	GRCh38.p7	17:80347839	CCCCCTCATTAACCG[A/G]CTGGAGAAGCACTAT	57674
rs775153175	snp	A/G	1.64866e-05	0.00287106	synonymous-codon	RNF213	GRCh38.p7	17:80289685	CAAGACCAAGGACGA[A/G]ATGGCTGCTGCTGAA	57674
rs775156188	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80295107	CCAGGTTGCAAATGG[A/G]AATGTGTAGAACTTT	57674
rs775157934	snp	A/G	1.70287e-05	0.00291788	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288168	GGAAGGGGAGGACCA[A/G]GACGCTTCCATCCCC	57674
rs775160450	snp	C/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80397990	CCCGAGGAGGATCAA[C/T]GCAGTGGCTGAACAC	57674
rs775168984	snp	A/G	1.64977e-05	0.00287203	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374545	GATGCTGTGGCCAAA[A/G]CTGTCCTCGAGTGCA	57674
rs775175802	snp	A/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80384059	TGGTTTTGAATAGGA[A/T]GTAGCAGAAGACTCA	57674
rs775178908	snp	A/C/T	3.31018e-05	0.00406817	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360042	AACCCTCTTCTTATC[A/C/T]TCCCTCACCTTATTG	57674
rs775185701	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383870	AGTACCTCCAGCACA[C/T]TGTGGAACAGAAAAA	57674
rs775188681	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364340	GCCTGGACCCCGGGT[C/T]CCGCATCTCTTCTCC	57674
rs775202047	snp	C/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363484	TGACGCTTCTCACAT[C/G]CTAGACAATGAAAGT	57674
rs775214525	snp	A/G			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320680	CAGGTGTGAGCCACC[A/G]CGCCCGGCCGAGCAT	57674
rs775226220	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80337257	CTGGCAGAATGATGG[C/T]GTCTGGTAGAGAGGC	57674
rs775228115	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80349166	AGTGGACATTGCTTC[A/G]TCATGACAGATACCG	57674
rs775230817	snp	A/G	3.30278e-05	0.0040636	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363142	GCACTAGGAAACTGA[A/G]AGCGGCGTCAGAAGC	57674
rs775233237	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364867	CCTGGCCTTTGGAGT[A/G]ACCCCAGAACAGACC	57674
rs775265240	snp	A/G	3.29527e-05	0.00405898	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353665	AACTCGGAGGCAGTG[A/G]TGTAAGTTCTGGTTC	57674
rs775267538	in-del	-/AG			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398712	GACAAAGAGGGAGTC[-/AG]AGAGAGAGAGAGAAA	57674
rs775269241	snp	G/T	1.65723e-05	0.00287852	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393547	GAGAGAAGACTCCTC[G/T]CTCCTCGTCTGCGGC	57674
rs775273082	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375060	AATCTAACCTTTAAA[C/T]TGGTCTGGTCTTGCT	57674
rs775273890	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80322162	CCCCCCACCCCCCCT[-/TT]TTTTTTTTTTTTTTT	57674
rs775289101	snp	C/G	0.000229938	0.0107199	intron-variant	RNF213	GRCh38.p7	17:80337792	GCCAGTCCAGGTCTT[C/G]TGGCCCCAAGAAAGT	57674
rs775302586	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RNF213	GRCh38.p7	17:80349823	TGAAATTTTAGAATC[A/G]GAGGTCACAGGCAGG	57674
rs775303077	snp	A/C	1.64792e-05	0.00287042	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380895	CGGAGAGACGTGGTG[A/C]CATGTGACCGAGGGC	57674
rs775316017	snp	A/G	1.65151e-05	0.00287355	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386807	GGAGGAGGGCAGAGA[A/G]ACCGTGCAGGAGTTC	57674
rs775329853	snp	C/T	8.25607e-05	0.00642445	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389321	AGCTGAATGTGTATA[C/T]TCAAGACATCCTGCA	57674
rs775343241	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80326391	CTGCCACCATCACAC[A/G]GGCAGTACCCTGTTA	57674
rs775343531	snp	G/T	1.75721e-05	0.00296407	synonymous-codon	RNF213	GRCh38.p7	17:80289775	GAACAGAAGTGCAGC[G/T]GCTGTGAAAAACGAG	57674
rs775359123	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80376357	CCTTTCACCTCCTGA[C/T]ATCAGCCGTTTTGCA	57674
rs775360250	snp	C/T	3.32309e-05	0.00407607	intron-variant	RNF213	GRCh38.p7	17:80349934	GCCTTCCCTGCTGCC[C/T]TCTCCCTCCCCAGCC	57674
rs775367784	snp	C/T	1.65121e-05	0.00287329	missense	RNF213	GRCh38.p7	17:80294978	AGGCACAGCTGTGGA[C/T]CGATTTGCAGTACAG	57674
rs775398232	snp	C/T	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80345174	GGAAGCACATGGTCA[C/T]CATGGATGGGGTTAG	57674
rs775429031	in-del	-/A	3.87695e-05	0.00440264	frameshift-variant	RNF213	GRCh38.p7	17:80289798	AAAACGAGAAGGAGC[-/A]AAAAAACCAGGAAGC	57674
rs775431499	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80307282	ATAATTGGCCGTGAC[A/C]CACATGTGCTGTTGT	57674
rs775432491	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80267950	TCAGCCTCCCAAGTA[G/T]CTGGGATTACAGGTG	57674
rs775450259	snp	C/T	1.64874e-05	0.00287113	missense	RNF213	GRCh38.p7	17:80347559	TTGGTTCTGGTTTCC[C/T]CAAGGACCAAGAGTA	57674
rs775452485	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366252	TTTTAGTTGTTTTGG[A/G]TATGTACCTTGAAGG	57674
rs775458343	snp	A/C	9.78617e-05	0.00699438	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288003	CCAGCCGAGCCAGCC[A/C]CCAGGCACAGCCACC	57674
rs775459040	snp	G/T	1.85266e-05	0.00304351	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372976	CGTTGGCCTCTCAGA[G/T]ATGGCCAAGGAGAAG	57674
rs775460209	snp	C/T	0.000185718	0.00963455	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80355265	CAGTGATAGGTTCGC[C/T]TTGGGCCTACAGCCA	57674
rs775468867	snp	A/G	1.65272e-05	0.0028746	intron-variant, missense	RNF213	GRCh38.p7	17:80319454	GCACCCTCCTCCCTC[A/G]CCAAGGGCAATGGCG	57674
rs775479127	snp	A/G	1.64909e-05	0.00287144	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364518	GTCCCCGAGTTACAG[A/G]GGCTGGTGACCGAGC	57674
rs775482959	snp	C/T	0.00020014	0.0100015	synonymous-codon	RNF213	GRCh38.p7	17:80332616	CTTCAGTGTTCTCAA[C/T]ACTTTACTAAATTTT	57674
rs775487867	snp	A/G			upstream-variant-2KB	RNF213	GRCh38.p7	17:80259372	ACTCGGGAGGCTGAG[A/G]CATGAGAATCACTTG	57674
rs775488668	snp	A/C/G/T	8.25482e-05	0.00642409	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389779	GTGCACGACATGAGT[A/C/G/T]GGGGTGTGAGACCTC	57674
rs775503657	in-del	-/TCT	4.97921e-05	0.00498935	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393327	CTGTTTTAAATGCTC[-/TCT]TCTTTGGTTTTTCAG	57674
rs775513383	snp	C/G	1.64757e-05	0.00287012	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369580	GTCCACCATTTGCTT[C/G]AAGGACAACGCTCCG	57674
rs775524126	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80278436	TTCGTGTGGAGGCCC[A/G]GGGCGCCGGGAGCCT	57674
rs775525015	snp	C/T	1.64727e-05	0.00286986	missense	RNF213	GRCh38.p7	17:80291695	AAGCACCTAGATAAA[C/T]ACATTCCTTACAAGT	57674
rs775537882	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80271340	TCTTGAGCTCTTGGC[C/T]ACGCCAACACTGAGT	57674
rs775539434	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80289248	TCCCGAGCGGGGAAG[G/T]GTCGTGAACATTCTG	57674
rs775550796	snp	A/C			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383509	ACATACATCTATAAA[A/C]AAACAACACTGAAAT	57674
rs775561914	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80391958	ACTTTTAGTAGAGAC[A/G]GGTTTCACCATGTTG	57674
rs775568210	snp	C/G/T	6.5982e-05	0.00574345	missense	RNF213	GRCh38.p7	17:80347465	TCCCGCTACTTACTC[C/G/T]TGCTGACCAAAAACT	57674
rs775572753	snp	A/G	8.38441e-05	0.00647418	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390222	GCACACCTATGGGGC[A/G]GGGCAGACACAATGT	57674
rs775585071	snp	C/T			intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80352228	AGTCTGAAATTAGAA[C/T]ATTATTGTTAACCTC	57674
rs775587724	snp	C/T	8.32175e-05	0.00644995	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319523	ACAGTCCCTGCTGCT[C/T]GCACCATCCTGCATG	57674
rs775609914	snp	C/T	0.000146424	0.00855514	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287908	CCTGCCAGCCCCTGT[C/T]ACCTGACTTTGCTTT	57674
rs775612318	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80277203	ATATGAAATATCCAC[A/G]ATAGACTCACCCATG	57674
rs775627824	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80283492	GTCTTTCCACAGCCC[C/T]GTGTTGTGGGCAGAG	57674
rs775629508	snp	C/T	3.2962e-05	0.00405954	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369522	CCATTGAAAAGCATG[C/T]CCGCTTCCGGCAGAT	57674
rs775651505	snp	C/T	1.73204e-05	0.00294277	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288387	TCCGGGAGAGATGGC[C/T]TGGGAGTGGCACTGA	57674
rs775651529	snp	C/G	1.64933e-05	0.00287165	synonymous-codon	RNF213	GRCh38.p7	17:80291790	CGAGTACGTCAACCG[C/G]TGTCTGTTCATAAAA	57674
rs775658092	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378829	TGGCACAATATCTGA[C/T]TTTGAAAAATAAGCC	57674
rs775675019	snp	C/T			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361969	ACGGAGACGTTTCCT[C/T]AGCTGCCTGGAGCTG	57674
rs775717813	snp	A/G	1.6651e-05	0.00288535	synonymous-codon	RNF213	GRCh38.p7	17:80273332	AGGGGGCCCGTGCTT[A/G]TTCCCGGGCTCAGAC	57674
rs775719348	snp	C/T	1.71302e-05	0.00292657	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363755	GCACATGCAAGGCAG[C/T]GGGAGCCTGGCCCAG	57674
rs775727669	snp	A/C	1.6489e-05	0.00287128	intron-variant	RNF213	GRCh38.p7	17:80319168	CGAAAGCTCTGAAAC[A/C]ACCCCCCTTTGATTT	57674
rs775728351	snp	C/T	4.98335e-05	0.00499142	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353079	GTCACGAGGCGGAGC[C/T]CCTGGGGGAGCAGGT	57674
rs775730763	in-del	-/T			intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320358	TGGTGGTGGTGGTTG[-/T]TTGTTGTTTTTGAGA	57674
rs775742673	snp	A/C	1.94793e-05	0.00312078	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363807	TGAGACCCAGGAGCC[A/C]TCACCCACTGCTTCA	57674
rs775742784	snp	G/T	1.64822e-05	0.00287068	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80363211	CCTACCAGCGTTTCA[G/T]AAGCCGTCTGCAGAA	57674
rs775770911	in-del	-/G	1.76724e-05	0.00297252	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372988	AGAGATGGCCAAGGA[-/G]AAGCAGTGCTACCTG	57674
rs775774361	snp	A/T	1.67301e-05	0.00289219	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388588	GGATTTAATTTTAAA[A/T]AACTTTTTTCTTTCC	57674
rs775775491	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80341188	AGGTGATCCGCCCAC[C/T]TCAGCCTCCCAAAGT	57674
rs775785209	snp	A/G	0.000191773	0.00979029	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374712	CCATCACGTGACACT[A/G]TATTGGAAGTCACGT	57674
rs775787416	snp	C/T	9.88452e-05	0.00702942	synonymous-codon	RNF213	GRCh38.p7	17:80319294	ATGCATCATTGAAGC[C/T]GTGAGCTCAGCCTGC	57674
rs775798926	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80324923	CCTTATAAAACAAGT[C/T]ACAGTAGATTTCAGA	57674
rs775817467	in-del	-/TCTC	1.65393e-05	0.00287565	frameshift-variant, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80369788	TGTGAACACACAAAA[-/TCTC]TCTCTCCATTCAATG	57674
rs775818521	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80272902	GTAGGGGAGGAAAGC[A/G]TAACAGGCTCTGTTT	57674
rs775822796	snp	G/T	1.64746e-05	0.00287002	missense	RNF213	GRCh38.p7	17:80345651	GCGACCTGCGGCGTG[G/T]TGGTACCAATGCTGA	57674
rs775831934	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80270547	ATCTTGTCAATCTGT[A/G]CCGGTCGTTGGGTGG	57674
rs775843559	snp	A/G	1.65162e-05	0.00287365	synonymous-codon	RNF213	GRCh38.p7	17:80348124	GCTGAACTGCGCTAC[A/G]CCCGATGCCGTGGTC	57674
rs775844219	snp	G/T	1.65089e-05	0.00287301	missense, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353007	TTCTGATGTGACCAG[G/T]CTGCAGCATGTCACC	57674
rs775861774	snp	A/G	0.000246305	0.0110947	missense	RNF213	GRCh38.p7	17:80339867	CAGCCCAACCTCGTC[A/G]TCTGTGGCCACTCCG	57674
rs775867186	snp	C/T	2.88663e-05	0.00379899	missense	RNF213	GRCh38.p7	17:80339967	TGCTGCTCTGCACCC[C/T]GGCAACCACCTTTGA	57674
rs775872380	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80307570	GTTTGTTTTTTTGAG[A/C]TGGAGTCTCACTCTT	57674
rs775879888	snp	C/T	1.67579e-05	0.00289459	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383060	CAGCTGTGATTTCTC[C/T]TGAACTGGAGGTAAG	57674
rs775901035	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80323778	TTAACAATGTTTTGT[A/G]TTTTTCATAGTTTAA	57674
rs775908521	snp	C/T	8.3398e-05	0.00645694	synonymous-codon	RNF213	GRCh38.p7	17:80346612	GATGGTCGTCTGCAT[C/T]GAGCTGAAGATTCCC	57674
rs775908794	snp	C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386964	CCTTGGTGTGTTTCT[C/T]GAGAGAGGGAAGCAG	57674
rs775919676	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80282316	TCCCCAGTATTTTCT[C/G]TCTGTGGTTGGCTGA	57674
rs775932728	snp	A/C	1.9238e-05	0.00310139	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386870	CCGCTTCCTCCAGGG[A/C]AAGCCCCGGCTGAGC	57674
rs775963692	snp	C/T	8.28658e-05	0.00643631	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361710	AGACGCACTCCAGGC[C/T]GCTCCTTGGTTTCCT	57674
rs775964107	snp	A/T	0.000115774	0.00760748	missense	RNF213	GRCh38.p7	17:80327839	GAGAAAATACTAGCA[A/T]ATGTCACAGAGGATG	57674
rs775968903	snp	A/C			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360993	CACCCCGCCCACTAG[A/C]AGCCAGATCTTTCTG	57674
rs775972267	snp	A/G			intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80371236	GCAACTAACCTCTAG[A/G]CATGACCATTTATCA	57674
rs775973536	snp	A/G	5.01266e-05	0.00500607	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360131	AACGCTTCCAACAAC[A/G]TCCCTTTCAGCTGGA	57674
rs775976173	snp	C/T	1.64846e-05	0.0028709	intron-variant	RNF213	GRCh38.p7	17:80307231	CGATGCAGTCTCTCC[C/T]TCACATGCGGCCCCC	57674
rs775981523	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80319029	TTGGTCTACTGGTGG[A/G]GGGCAGGGAGGACAT	57674
rs775993745	snp	C/T	1.71182e-05	0.00292554	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80371905	GATTATATTCAGGAA[C/T]ATTTGACCCTGTTAA	57674
rs776006527	snp	A/T			utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80396058	GCCCTACCTTGGTGG[A/T]GATTTACCTGAAAAT	57674
rs776011536	snp	G/T	1.64732e-05	0.0028699	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80385127	AGAACGTCCAGCAAG[G/T]TGAATACAGCTCCAT	57674
rs776022162	snp	C/T	1.67492e-05	0.00289384	stop-gained, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372626	CCAGCAAGCCGGGGC[C/T]GAGAGCCTGCCAACG	57674
rs776039765	snp	C/T	1.70249e-05	0.00291756	synonymous-codon	RNF213	GRCh38.p7	17:80347203	CGGGCTTCGTGACTA[C/T]TACAGCCTCATCAAA	57674
rs776048832	snp	A/G	6.86318e-05	0.00585758	missense	RNF213	GRCh38.p7	17:80340129	GCACGCAGCAGCACC[A/G]AGAAGACTACCAGCT	57674
rs776058156	snp	C/T			intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370267	AAGTTTCTATTCCCC[C/T]GAACATGGGCTCTAT	57674
rs776063953	snp	A/C	0.000115313	0.0075923	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377840	GAGGGGTGGCGTGCA[A/C]TCCTGGGTTGGAGGA	57674
rs776077131	snp	A/C	4.94246e-05	0.0049709	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80375776	CCTGCAAGACCCCCC[A/C]AAGCCAGCAGTCAGC	57674
rs776081814	snp	A/G	4.96824e-05	0.00498385	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364602	GATCCACCCTTTTCC[A/G]AAAGGAAGAACAGCA	57674
rs776086314	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80292313	CCTCAGGTGATCTGC[C/T]CTCCTCGACCTCCCG	57674
rs776091123	snp	C/G	1.6477e-05	0.00287024	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353683	TAAGTTCTGGTTCTT[C/G]GGACCTCCCCTTGTG	57674
rs776100667	snp	C/T	4.97682e-05	0.00498815	missense	RNF213	GRCh38.p7	17:80295644	TTGCCTGTGGACTGC[C/T]CAGTGAGGAGTAAAC	57674
rs776114461	snp	C/T	4.94181e-05	0.00497057	missense	RNF213	GRCh38.p7	17:80345099	TCGTGGTGACCTTCA[C/T]GATCTTTATGGCAAG	57674
rs776161329	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80317557	TGGACTTGCGACAGG[C/G]ATGCTGTGTTTACTT	57674
rs776162319	snp	A/G	6.60197e-05	0.00574504	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374554	GCCAAAGCTGTCCTC[A/G]AGTGCAAGCCACTGG	57674
rs776174312	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80304701	ATTATTGGGGTATAT[C/T]CCTTTTATTGTAAAA	57674
rs776175928	snp	A/G	0.000114923	0.00757946	missense	RNF213	GRCh38.p7	17:80339540	CCCCCGAGTGATGCC[A/G]CCCTAACGATGCTAT	57674
rs776179897	in-del	-/AAG	1.64914e-05	0.00287149	cds-indel, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80393380	GTTACATGCAAACTA[-/AAG]AAAGTGAAATTCTTC	57674
rs776195392	snp	C/T	3.29533e-05	0.00405901	missense, intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361796	AGGTTTCTTGCCCAG[C/T]TCCATGGAGAGCCGC	57674
rs776209147	snp	A/C/T			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389138	TGCCAGAAACCCAGC[A/C/T]CACAGACATCCCTCT	57674
rs776210279	snp	G/T			intron-variant	RNF213	GRCh38.p7	17:80263959	ACCACAGAGTCTGTT[G/T]TGGGGTGGCATAGAT	57674
rs776211801	snp	C/T	3.29495e-05	0.00405877	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383886	TGTGGAACAGAAAAA[C/T]GGCAAAGAAAGAGTG	57674
rs776212797	snp	C/T	1.67435e-05	0.00289335	intron-variant	RNF213	GRCh38.p7	17:80295538	TGGTTCATGCATCTT[C/T]CTCTTCTCCCACCAT	57674
rs776228650	snp	C/T	1.65436e-05	0.00287602	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80360052	TTATCATCCCTCACC[C/T]TATTGCAGACATAAA	57674
rs776230866	snp	A/T	1.93343e-05	0.00310915	missense	RNF213	GRCh38.p7	17:80289798	AAAACGAGAAGGAGC[A/T]AAAAAACCAGGAAGC	57674
rs776247891	snp	A/T			intron-variant	RNF213	GRCh38.p7	17:80327172	TCCTAGGGCAGGGGC[A/T]TTTTAAAGAAGATTC	57674
rs776250900	snp	C/T	0.000116952	0.00764607	missense	RNF213	GRCh38.p7	17:80339298	CCATGGCCTACTGCT[C/T]CCCCAAGCAGGGTGT	57674
rs776256968	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80344284	GTCTGAATCCCAGCT[C/G]TGCTCTGAATCTAGG	57674
rs776260634	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80302893	CTTTCTCTTTAAGTA[C/T]AATCTCTCTGAAATA	57674
rs776269480	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80318166	CCAAGTCTGGGGTCT[C/T]TATAGGCACAAGATA	57674
rs776281731	snp	C/G	4.98285e-05	0.00499117	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372001	GTAAGTGAACTCTCT[C/G]TTCCCTGAATTTCTT	57674
rs776289502	snp	A/G	3.44738e-05	0.00415159	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288342	GACCACCGAGCAACA[A/G]GCAGGGGCCTCAGCC	57674
rs776295572	snp	A/G	1.65411e-05	0.00287581	missense	RNF213	GRCh38.p7	17:80348014	CACTCGGACGCCTGC[A/G]CGTCTGTGGTGCTGC	57674
rs776300165	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80286561	GGGGCTCCTGAAGTG[A/G]CAGTGATGGGATCCT	57674
rs776305834	in-del	-/GC			intron-variant	RNF213	GRCh38.p7	17:80290389	TGCGTGCACGTGTGT[-/GC]GTGTACGTGTGCTTG	57674
rs776328404	snp	A/G			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389770	GGCTCCCTGGTGCAC[A/G]ACATGAGTGGGGGTG	57674
rs776341737	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80262089	GAGAAGGAAACACTT[C/T]GGGTGGAAAGAAAGA	57674
rs776358704	snp	A/G			synonymous-codon	RNF213	GRCh38.p7	17:80327922	CCTCCTAAGTGGCAC[A/G]ATTTTAGTTGGACAA	57674
rs776362268	snp	A/G	6.63933e-05	0.00576127	missense	RNF213	GRCh38.p7	17:80350324	TAACGAATACAGCCA[A/G]ATGTAAAATCCTCAT	57674
rs776374993	snp	A/G/T	3.30667e-05	0.00406602	intron-variant, synonymous-codon, missense	RNF213	GRCh38.p7	17:80319459	CTCCTCCCTCGCCAA[A/G/T]GGCAATGGCGCTGAA	57674
rs776380431	snp	C/T			intron-variant	RNF213	GRCh38.p7	17:80329190	CCCCTCCCCCGCTAC[C/T]CACTCCTGCTTCCTC	57674
rs776390324	snp	C/T	3.2963e-05	0.00405961	missense, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380916	GACCGAGGGCTGCCC[C/T]CAGTGGTCTTCCTCC	57674
rs776390356	snp	C/T	1.64751e-05	0.00287007	synonymous-codon	RNF213	GRCh38.p7	17:80346154	GTTGAGTCCATCAGC[C/T]TAGATGAAAACGGGA	57674
rs776406778	snp	C/T	8.24708e-05	0.00642095	intron-variant, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80354430	GAACGTCTGTTTCTG[C/T]CTTTGTACAGCCTCT	57674
rs776408766	in-del	-/TT			intron-variant	RNF213	GRCh38.p7	17:80267814	CTACTCAACAGCAGA[-/TT]TTTTCTTTTCTTTTT	57674
rs776410136	snp	A/G	1.69763e-05	0.0029134	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383078	AACTGGAGGTAAGCA[A/G]TAAGTGCTGACAGCT	57674
rs776410271	snp	C/T	3.33611e-05	0.00408405	synonymous-codon	RNF213	GRCh38.p7	17:80346616	GTCGTCTGCATCGAG[C/T]TGAAGATTCCCCTCT	57674
rs776418150	snp	C/T	4.98211e-05	0.0049908	intron-variant	RNF213	GRCh38.p7	17:80349940	CCTGCTGCCCTCTCC[C/T]TCCCCAGCCGCAGCC	57674
rs776422810	snp	C/T	3.69201e-05	0.00429636	synonymous-codon	RNF213	GRCh38.p7	17:80343313	GCTCTTTCACCTGGA[C/T]GTGACCTCCTCAGTA	57674
rs776445462	snp	A/G	0.00014921	0.00863614	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80383980	GTGCAGAGTTCCCCA[A/G]CAGGCCTGAAGGCCC	57674
rs776455510	snp	C/G			intron-variant	RNF213	GRCh38.p7	17:80264719	CAGCAGACAGTCAAA[C/G]CACAGACCCCCTTAC	57674
rs776456773	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80337341	CCCCATGTGCCAGCC[A/G]GGGCACCAGGCACTG	57674
rs776464291	in-del	-/G			intron-variant	RNF213	GRCh38.p7	17:80263492	AGCACAGAGCGGGGA[-/G]GGGGCTGGGCTTGGG	57674
rs776465973	in-del	-/AAAC			intron-variant	RNF213	GRCh38.p7	17:80297007	AAAAAACAACCAAAT[-/AAAC]GCCGCACATTTTGAC	57674

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