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

RNF217

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs140730045	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125004363	GTGCCATTACTTATG[C/T]CCTTACCCTTGGATT	154214
rs140733041	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125078081	TTTCCACAGCCAATA[A/G]CATTCAATAGTCAAG	154214
rs140751441	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125001346	TGCTTTTGAGGTCAG[C/T]AGTAAATGGAGTTGT	154214
rs140804633	snp	A/T	0.00202928	0.0317887	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081542	TCTGAGATTAGAATT[A/T]TCTGAGGGCCATAGA	154214
rs140840214	snp	A/G	0.0193772	0.0965046	intron-variant	RNF217	GRCh38.p7	6:124997686	CGATGAGATACCTGG[A/G]CACTAGTTTCAGGGT	154214
rs140898694	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965810	CCTCACCCCACGCTC[G/T]CTCTCTTTTTTCCTG	154214
rs140904347	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124983625	CTAACGATGTTTTCA[C/G]CCCTAGTGAAATTAA	154214
rs140907074	snp	C/T	0.0209421	0.100162	intron-variant	RNF217	GRCh38.p7	6:125060633	TTTCTTCAGTAGAGA[C/T]GGGGTTTCACCATGT	154214
rs140977351	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974066	CAGGCTGGCCTCCCC[C/T]GGAGCCAGCATCCCA	154214
rs140982501	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053695	TTAGGGCAGGTGAGT[C/T]GGCGTACTTTCATCT	154214
rs140982937	in-del	-/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125077722	CATCACATGGATGTC[-/T]GTTAGAATTCCTTTT	154214
rs141020415	snp	A/G	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125020373	TCTGTTATTAAAAGG[A/G]TAGAGAATGTGAAAT	154214
rs141088533	snp	A/G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125049115	TTTCTAACCTGAATA[A/G/T]TTCCTGTAATTTATC	154214
rs141097450	snp	A/G	0.0267878	0.112589	intron-variant	RNF217	GRCh38.p7	6:125021629	TTCAGAGTACATGTA[A/G]AATAAATATATTCTA	154214
rs141109595	snp	A/C	0.000168305	0.00917192	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125081449	AGCTGGAAAATTATT[A/C]ATTGCACCTCTAATT	154214
rs141174304	in-del	-/CCT	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125067895	GTGAAGGAACAGGAA[-/CCT]ACCTCAGAGAGGAGA	154214
rs141186217	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018813	TCTCCCAGAGTAATG[A/C]AGACTGGAGGTGTGC	154214
rs141218634	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017586	CTTATTATGAGAAGT[A/G]TTCACATTTCTCTGC	154214
rs141220596	snp	G/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125059587	CAACTGGATTTGGAA[G/T]GAGCACCACTGCAGC	154214
rs141227087	in-del	-/AG	0.477853	0.102875	intron-variant	RNF217	GRCh38.p7	6:125072854	GCATAATAAAGAAAC[-/AG]ACATGGATTCAAAAT	154214
rs141261410	snp	C/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124972589	ACTGTCCCACTACAC[C/T]TATAGAGATATTAAA	154214
rs141289437	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124992417	AAACTAAGAGGCTAT[A/G]GAACATTGATTTTAA	154214
rs141318923	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087925	TACCAGTTTTGCACA[C/G]CAATCCCAAGTTTAA	154214
rs141319026	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125021327	GCTGGAGTGCAATGG[C/T]GCGATCTTGGCTCAC	154214
rs141353913	snp	A/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124989281	TCTCACTGCATAATA[A/T]ACAAAGTTATTTGCC	154214
rs141392274	snp	C/T	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:125076594	GTTTCATAAAATTTG[C/T]GATTTTGCTTTTTAA	154214
rs141416494	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009066	CTGGTTCATAGAGAA[C/G/T]AAGGAAGTAGATAGA	154214
rs141482303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070162	CTCCAGCTCCATCCA[A/G]GTTTCTGCAAAAGAC	154214
rs141521976	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124999788	ACTTAGCATTGTAAC[A/G]TTAAAAAAAAATCCA	154214
rs141527362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077197	GGACAATATCCAGCA[A/G]CAGGTCGTACACATA	154214
rs141560178	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023754	TCTTTAGAAAGAAGG[A/G]AATACTGTCATTTGC	154214
rs141593075	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125062925	ACACCATTTTTTATC[C/T]TAACAATGAGTTTTC	154214
rs141612956	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092390	TGGTTGGGCTTTTAT[A/G]AAAAATTATTTTCGG	154214
rs141667222	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125055046	TCTGTATGTGTTTGC[A/G]TAAGGCCAATTTTGA	154214
rs141673911	snp	C/T	0.0248432	0.108648	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087035	CTGCTATTCTAACTA[C/T]TCCTCTTCACTGAAG	154214
rs141674422	snp	A/G	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124976373	TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	154214
rs141704947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990050	CAATCAAGCTTTGCC[C/T]CTACCTCTCCACTGT	154214
rs141731945	in-del	-/C	0.0310518	0.120672	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087305	ATGTATGCCAAAAAA[-/C]GTTTTTAGATTTTAA	154214
rs141752149	snp	A/G	0.0225045	0.103662	intron-variant	RNF217	GRCh38.p7	6:125049791	TAGTTGAAAGAAAAC[A/G]TGGGGTGAGTGGTGG	154214
rs141768440	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970867	ACAGTGTTTTAAAAG[G/T]GATAATCACATGTGT	154214
rs141770098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050944	TTGATAGACGCCAGT[A/G]TAAACAAAGTGTGTG	154214
rs141812767	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125013573	AAAAAGTAGTCTGAA[A/G]GCTTTGGCTGTTTTC	154214
rs141836629	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125073631	GTTGGTAACTCTCGA[A/C]CCTAGGTGCTTATAT	154214
rs141840677	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124968463	TTCTTTTTTCTTTTC[C/T]TTGTTCTTTTACTTT	154214
rs141876081	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082772	CTTCTTTGTATGTTC[A/G]TACACTGCAAATAAA	154214
rs141899863	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053059	TGGGCCTCTGTGTGG[C/T]GGCTCAGGATGGACC	154214
rs141934722	snp	A/G	1.65395e-05	0.00287567	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045331	TATAAGTACTTCTTG[A/G]AACTTGGCCGTATTG	154214
rs141948041	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040515	TCTACCAGAGGTACA[A/G]AGGAGCTAATATCAT	154214
rs142023208	snp	C/T	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:125030028	GCCTCAGAATCATGG[C/T]GGGAGGTGAAAGGCA	154214
rs142055001	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125011257	ATATTACATGTAATT[A/G]GCTCTCACCTCCAAT	154214
rs142117085	snp	A/C	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125065894	CCAAATAGCTACTCA[A/C]CATCTTCAACCGGAT	154214
rs142124188	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125013551	CAGAATATGTCTGGG[-/A]AAAAAAAAAAAGTAG	154214
rs142154642	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125031943	TTGGACTTACAGTTC[C/T]GCATGTCTGGGGAGG	154214
rs142164259	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:125080824	GTGCTTCCTTTTTCA[A/G]TTCGTTAAAATGATT	154214
rs142169960	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125030550	CAAAGGGTTTAGAGC[A/G]CCCATGCAAGTCCAA	154214
rs142171698	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125001521	TAATTAAAATGTGAC[A/C]ATTGAAATAATTAAG	154214
rs142220220	snp	A/T	0.000153988	0.00877328	intron-variant, missense	RNF217	GRCh38.p7	6:125082496	AGTGGTAGAACCAGG[A/T]ATCAAACCCAACATT	154214
rs142228859	snp	A/C	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125064745	AAATGAGGACAAAAT[A/C]AGTACGTGTGTATAT	154214
rs142232607	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124990352	CTTTCTAATTTATAT[C/T]CCGAGCTCAGACAGT	154214
rs142249856	snp	A/G	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124987974	AGATTAAGTGTCCCC[A/G]ATCCAGGGATCAATC	154214
rs142295720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037502	GATTTCTGGAATTTT[C/T]GGCTTGATTTTTTAA	154214
rs142302319	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056384	AATATATTCAACATA[A/G]ACATTATCATTGAAC	154214
rs142314492	snp	A/G	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:124978498	CGTGGAGCCCCAAGG[A/G]GGGTTACAGTTCTCG	154214
rs142364966	snp	C/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124991556	TTGTCTTTTTCTCCC[C/T]GCAAGGCTGTAGGCC	154214
rs142367334	in-del	-/TTTGAG			intron-variant	RNF217	GRCh38.p7	6:124989638	TGTAAACACTTAAAT[-/TTTGAG]TTGATATAATTTTCA	154214
rs142369041	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125068612	TTTTTTCATGCATTT[A/G]GCATAGCTTATGCAT	154214
rs142432271	snp	A/C	0.0197687	0.0974348	intron-variant	RNF217	GRCh38.p7	6:125052926	GCCAGGATTATAGGA[A/C]CTTACTGGCTCCATT	154214
rs142498466	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967268	CCCTCCTAAGTATTG[A/G]CCTTCTCAGCTGACT	154214
rs142498734	snp	A/C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125015908	GAATATAATGTAGCA[A/C/T]TTCAGCAAAAAAAAT	154214
rs142516767	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124970091	AAGACAGCAGGAGGA[A/G]TGGGGAAAGCTGGTC	154214
rs142544995	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086220	TTGTACAGGAGTGCA[G/T]AATTTTTAAAGAAAA	154214
rs142554675	snp	G/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089698	ACCCCAGAAATTGCT[G/T]AAATGTCCTTTTAGA	154214
rs142559871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011880	AATAACTGCCAGCCC[C/T]AGTTTTTGGTGCTGA	154214
rs142571984	snp	C/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125013962	ACTACATGTGCAAGT[C/T]ATACTGTCATCCTGT	154214
rs142610684	snp	A/G	0.00512948	0.0503828	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058056	TTGCGTCACTGGGCC[A/G]GCGAAATTGAGCATG	154214
rs142612590	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125041514	ACTTCATCTCATACT[C/G]TTCTCTCCCTCCTTT	154214
rs142636568	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124970398	ACTGACAGAATGCCA[A/G]TGATTGCACATGGGA	154214
rs142707166	snp	G/T	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:124969596	TTGGACATCTATCTT[G/T]TAAACATTCTTACAT	154214
rs142709206	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125017912	GAAAGAATTCACTTT[A/G]TAAAAGAGGGTACCA	154214
rs142722483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997266	TGTATGGCTGCTTCA[C/T]TACTCGCATGTTCCC	154214
rs142734119	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125062447	ATGATTTTTATAGTA[C/T]GATAAAAATATACAA	154214
rs142743736	snp	A/G	0.0123036	0.0774623	intron-variant	RNF217	GRCh38.p7	6:124984501	CTGCAGTGCGTTGTG[A/G]TCACACCTCCAGCCT	154214
rs142767250	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125058283	ATTTTTATAAACCAT[A/G]TATATTCTTATTTTT	154214
rs142777108	snp	A/C	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124980655	GCTTAACCATACAAT[A/C]GCTGTTTTGATCGTG	154214
rs142844401	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125020935	ATTTTTTCATTTGTA[A/T]GCTTATTTTTCTAAA	154214
rs142886733	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125032982	CCAAATTACACGTGA[A/G]TGTGGTTTTATTGTA	154214
rs142945613	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067820	AAACCATTCGAATGT[A/G]GAAGTGATCACTCAA	154214
rs142955650	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981536	TTGAGTCCTTGATCA[A/G]CCATTCACTGAATAT	154214
rs142960269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990940	TGGGCACAGTAGCTC[A/G]TTCCTGTAGTCCTAG	154214
rs142988423	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083257	AAGAATTCTGAGCAC[A/G]CCTCTTCTGAGAATT	154214
rs143073409	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125044166	TTTCTACTCCAAGTG[C/T]GCATGTTTTGCTTTC	154214
rs143089327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070792	AGGAAACACATATAT[A/G]AAAATACTTTCAAAA	154214
rs143099223	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124992894	ATCTTTTACCTAAAA[C/T]GATTTATGTCTTTGA	154214
rs143108274	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124993576	GCAAAGGTGAACCTG[A/C]CATGTTTTTAAGTCA	154214
rs143152789	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125057562	ATTCTTAAGAAGACA[A/G]TGGAAATGGCTGGGT	154214
rs143153549	snp	C/T	0.0174175	0.0916809	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964475	GCTTCATGTTGAGTC[C/T]CTTGCCCATCATAGT	154214
rs143160470	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026423	GGCACATACTAAACG[C/T]TCAACAAATGTTAGC	154214
rs143164129	snp	A/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084754	GGTTTGGGAATAGCA[A/T]ATTTCTAAAGCATAA	154214
rs143226366	snp	G/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125050061	GGAGGTAGAGGAGGT[G/T]ATAGCAGTTCTTTAT	154214
rs143231754	snp	C/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124969766	GGAAAATGAGATAAG[C/T]AAATTATTTAGCTTA	154214
rs143235646	snp	A/C	0.0142736	0.0832652	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971563	CAGGTTCAAGCGATT[A/C]TCCTGCCTCAGCCTT	154214
rs143243943	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047320	TTTAAGTCACAATTA[C/T]GGCAATAGTGAAATG	154214
rs143297354	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124966629	AATAAAAGAGTCCCT[A/G]TTAAACATTTTATGC	154214
rs143307745	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090209	ATTTACCTTGACAAG[A/G]ACAATCTGTTACAGA	154214
rs143328651	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125043959	CTTTTCTGGTATTCA[A/G]TATGTCACCCCATGC	154214
rs143430041	snp	C/T	0.0524604	0.153226	intron-variant	RNF217	GRCh38.p7	6:125062765	TATTTTTAGTAGAGA[C/T]GAGGTTTCACCACGT	154214
rs143476954	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125023133	CTTGTTAAGGATCAC[C/T]TGATACAGTTTTGAG	154214
rs143509586	snp	C/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125029282	ATTAAACATCAAAAG[C/T]AAAGACAGCTTTTTA	154214
rs143577858	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125023403	AGTATTTTAATTAGT[A/G]GAGTTGTATGATCAG	154214
rs143589582	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982608	CTTATAATCATTGCC[A/G]TTTTATAGATCATTT	154214
rs143621967	snp	A/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125030347	AACAGTCCCCCAAAG[A/T]CTTAACTCATTTCAG	154214
rs143647165	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087452	GGTCTGCTTTATTGT[G/T]TTGTGTTAATATCTA	154214
rs143655418	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125013074	CTTGAAATAATTGAC[A/C]TTTAGTTCTGATTTT	154214
rs143667379	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030058	ATTTCTTACATGGCA[G/T]CAGCAAGAGAAAATG	154214
rs143694192	in-del	-/TGTG			intron-variant	RNF217	GRCh38.p7	6:125013352	TGCATGTTTTGTGTA[-/TGTG]TGTGTGTGTGTGTGT	154214
rs143753377	snp	A/G	0.000697068	0.018656	intron-variant	RNF217	GRCh38.p7	6:125082445	TATTATCTGTATTAT[A/G]CAGTTGAGGAAATTA	154214
rs143758706	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973917	GGGGTTTCTCATTTG[A/G]TTGTAGTCAGATGTC	154214
rs143809554	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981953	GAACCACTTGAACCC[A/G]GGAGGCAGAGGTTGC	154214
rs143842584	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125044548	ATTTTGTAAATTACC[A/G]CAGTAGCAGCCAGAT	154214
rs143852863	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052562	AATATCAGGGAGTAA[G/T]ATTAAAGACAAGAAG	154214
rs143906823	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007201	CATTTTTTCATGCAG[A/C]CTTCTTCTTGCCTAA	154214
rs144013973	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125017938	TACCACATATTTTCA[C/T]GAATCACATTTTCTG	154214
rs144016453	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124989868	ATTGTTCTCTGCTTG[-/A]GAAAAAAAAAACACC	154214
rs144022154	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125047265	TAACTGAGTAACTTT[C/T]AAATGTGTTGTTTTT	154214
rs144026718	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125010377	AATGTGCTTTTTAGG[A/T]ATAATGCATGAAGTG	154214
rs144043596	in-del	-/CTT	0.0659073	0.169145	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963440	AGGTAACTTCACCCC[-/CTT]TCTCTTCCCCATTTA	154214
rs144050159	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125081101	ATCTTTTAGCATTGC[A/G]AACATTGAAAATGGA	154214
rs144062121	snp	C/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125003690	AATATCACATTATAC[C/G]TTATAAATATGTATA	154214
rs144065919	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058730	TTAGCCAAGCAAACA[G/T]CCAGGGAAGACTCTC	154214
rs144101351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965249	CCTGACCTTCTTCCA[A/G]AGTATTTGCTGGGAC	154214
rs144166962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001439	GGCACAGAGAATCCC[A/G]TATTAATGTTACCAC	154214
rs144210078	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124976624	CTTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	154214
rs144239933	in-del	-/TTCT	0.0166325	0.0896639	intron-variant	RNF217	GRCh38.p7	6:125081076	CTCAAAATGTGCCAC[-/TTCT]TTCTTAATCTTTTAG	154214
rs144241479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063277	AACACAGGATTATAC[A/G]TTATAAAAGCAAATA	154214
rs144257879	snp	A/G	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:124987370	TACCCATTATTCATC[A/G]TTCCCTGCCCTCACC	154214
rs144265681	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124991219	TGACTCCATTTTCTA[C/T]TCCTCCTGCCATTGC	154214
rs144308512	snp	A/C	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125059477	CCAGTAGGAACTTAG[A/C]GTGCTGTTAAGTTAT	154214
rs144327163	snp	C/T	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982109	AGGTATGTAGCTATG[C/T]AGCTTTTTTATTTTT	154214
rs144367584	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124985977	AAAATTCATGTGTTG[A/G]AACTCAGCCATCAAT	154214
rs144404067	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125035970	ATGTGCAGGATTGTT[A/G]CATAGGTATACATGT	154214
rs144425894	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090484	CCAAATAGAGTAAAA[C/T]ATTAAAGAGAAAAAA	154214
rs144434667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014898	TTGAGCAAACCCAAA[A/G]CCCCTTCCTAATAAA	154214
rs144462310	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125029991	GTATAATTGGACTTA[A/C]GAGTTACACGTGGCT	154214
rs144483954	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124992116	TACTTTTACAATTCA[A/G]ACAAGCTACAAAGTA	154214
rs144529060	snp	A/G	0.00914312	0.0669923	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083729	ACAACAGGCCATTTC[A/G]ATACTGAACTTTTCT	154214
rs144547634	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124975545	AAGCAATCCTCCCAC[C/T]TCAGCCTCTCGAATA	154214
rs144569214	in-del	-/T	0.0271762	0.113356	intron-variant	RNF217	GRCh38.p7	6:125023602	GAAATGAAATTAGTA[-/T]GTTGAAGAGATATCT	154214
rs144598712	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF217-AS1, RNF217	GRCh38.p7	6:124960534	AGCTGGAACCTAAGG[A/G]ATAAGGAATAAAATG	154214
rs144603046	snp	A/G	0	0	intron-variant	RNF217	GRCh38.p7	6:125039918	GGACAAAGAGACAAC[A/G]TACCAGAATCTCTGG	154214
rs144607510	snp	C/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125038315	AGAAGTTAGATGACA[C/T]GTTATTTAGAATGTT	154214
rs144610844	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041414	CCTCCTCATAAAACC[A/T]GTGATTTGTATTGTC	154214
rs144631728	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965089	ACCTCATAAGTTAGT[C/T]TTAGGAAGTTTTAGT	154214
rs144735209	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072883	ATCTTTCTCACTCAC[A/G]AGGATTATCACTCAG	154214
rs144743292	snp	A/G	0.00835141	0.0640778	intron-variant	RNF217	GRCh38.p7	6:124995261	GTTTTAAAAACAATA[A/G]TAAAATGAAAGCTCA	154214
rs144800984	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091798	TTCATACAGATGCTA[A/G]AGAACCATGGTGTCT	154214
rs144815523	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125016036	TGGTACATAAAAATA[C/T]AAGGAAGCCCACGAA	154214
rs144836903	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124974894	ATAGATGTTGTCCTC[A/G]AGTTTCTTCCTGTTA	154214
rs144840539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067127	GAGGGAGATTACAAT[C/T]AAAACTGCAAAGGCA	154214
rs144843351	snp	A/G	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:125054346	AAGGCTCCATGGGGA[A/G]CAGGAAGGGCAGGAA	154214
rs144881550	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124973218	GTGGATAAGATTTGG[C/T]CTCTGCATCCTCTTC	154214
rs144892336	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124973522	GAGAATAGGTGCTCA[A/G]TAAATATTTGTTAAA	154214
rs145037937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019729	CTCTGTCTTTCTCCA[A/G]CACTTACTGGTGCTA	154214
rs145038563	snp	C/T	0.0178098	0.0926698	intron-variant	RNF217	GRCh38.p7	6:124992735	CTTTAGCAGAACATT[C/T]TTTGTTGTAATGATT	154214
rs145141384	snp	G/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081625	TTTATGTTGTATGCC[G/T]GCTTTAGATAGATTA	154214
rs145141537	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125037023	GAAAGACAGGGTGGC[A/G]ATTCTTCAAGACTGA	154214
rs145174431	snp	A/G	1.65444e-05	0.00287609	intron-variant	RNF217	GRCh38.p7	6:125076882	CTGACATACTTATGG[A/G]TGTCTTCCCTGGGAA	154214
rs145216221	snp	A/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125075919	TGTTATATATGGTGT[A/T]TGTATATATACCATA	154214
rs145221592	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125030206	GTCCCTCCCACAACA[C/T]GTAGGAATTCTGAGA	154214
rs145233874	snp	A/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124998263	TGGATTCACCTTGTA[A/T]GTCATTTACATTTGC	154214
rs145235175	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125070387	GCAGCAGGATTGCTG[A/G]ATCAAATGATAGCTT	154214
rs145270781	snp	A/G	0.110167	0.207236	intron-variant	RNF217	GRCh38.p7	6:125034370	CTTGAATTAATTTTT[A/G]TATAAGGTGTAAGGA	154214
rs145293258	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085907	TACCTTTCCATAAGC[A/G]TTTAAATAGATTTAC	154214
rs145316394	snp	C/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125074226	TGTGTTCCACTTAAT[C/T]ATTACTTCTTCAAAA	154214
rs145330926	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124978364	GATCCTGTGCCCACC[A/G]TGGCTCTGCGCTCAG	154214
rs145401407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125043716	GAATTATAATAGCAT[C/T]GTAACACTGTAACAT	154214
rs145471310	in-del	-/ACCTTACCATTGGTAAGTAGCTTTCTT			intron-variant	RNF217	GRCh38.p7	6:124989033	ATTTTTTTATAAGCA[-/ACCTTACCATTGGTAAGTAGCTTTCTT]TATATCTGCTACAAT	154214
rs145506518	snp	A/G	0.0150606	0.0854603	intron-variant	RNF217	GRCh38.p7	6:125075407	TTGACTCATGGTTCC[A/G]CATGCCTGGGGAGGC	154214
rs145514839	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017632	TATCTGTTCTATAGG[C/T]CTTTAAGCTCAAGTC	154214
rs145515291	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060201	TACCATTTATAAATA[C/T]AAAATAGGAAGATGG	154214
rs145525596	snp	A/G	0.0287284	0.116357	intron-variant	RNF217	GRCh38.p7	6:124969990	TGTAAAGTTCCAAAG[A/G]TAGAAGCATACGTGT	154214
rs145579559	snp	A/G	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125036129	CCCCTCCCTGTGTCC[A/G]TGTGTTCTAATCGTT	154214
rs145581231	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125057350	ACATGCCCACCTAAT[A/T]TTTATATTTTTCGTA	154214
rs145625597	snp	C/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125056810	TAAGTCAGGTTATAC[C/T]CATATGCTTTTAGAG	154214
rs145633019	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125015530	ACTTTAAGCTATTTT[A/G]GAAAAGAAAAGCGGT	154214
rs145634805	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978785	TCTGGGCTGTTGTCC[C/G]CTGACCAAGAGGAAT	154214
rs145723877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064234	GCTTTTCCCTAACTA[C/T]TGATAAACCATTTTT	154214
rs145733220	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124987735	CCTGCCTCAACCCGT[A/G]GAATAGCTGGGACTA	154214
rs145794591	snp	A/G	0.00993419	0.0697739	intron-variant	RNF217	GRCh38.p7	6:125020734	CTCCATGAATACTGT[A/G]TACTATGTATGGACT	154214
rs145826610	snp	A/G	0.0513262	0.151752	intron-variant	RNF217	GRCh38.p7	6:125030765	CTTTTCCAGGCACAC[A/G]GTGCAAGCTGTCGGT	154214
rs145839863	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125059068	GTATATTCTAAGCCT[A/G]TAAATGAGCATAATA	154214
rs145852712	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124993446	TTTGGTTAGGTTTTC[C/T]TTTCTTTGATGAAGA	154214
rs145861647	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081743	TGTACCTTATAAAGC[A/G]TTATTAACCCTTTTA	154214
rs145869628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005509	AAAGTCATGATAAAA[A/G]CAGGTATGTTTGGAT	154214
rs145903989	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125003112	CACACACGCACACAA[-/AC]ACACACACACACACA	154214
rs145905158	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125040358	GAAATGGATAAATCC[A/C]TGGACACATACACCC	154214
rs145943502	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124983772	CTATAAGACTCTTGG[A/G]AAAGATACTTAATGG	154214
rs145972510	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084170	AGGATTTTTTCTTAC[A/C]TTTAACTGCTCAAAC	154214
rs145992160	snp	A/T	0.0158469	0.0875917	intron-variant	RNF217	GRCh38.p7	6:124969663	ATACTTATTACATAC[A/T]AGGCACTGTTTTAGG	154214
rs146011768	snp	A/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125014046	TGTTCTCTGAATGGG[A/T]ACTGACTCTGGATTT	154214
rs146014459	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089865	ACTTCTTCAATATCC[A/C]CATATATTTGTATTG	154214
rs146034634	snp	A/C	0.00517822	0.0506191	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971930	GTGGGGCCATCTTAC[A/C]CACTCTCATGGTTTC	154214
rs146038020	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125051207	CTAAAAAAACAAACT[A/G]TAGTAATAATCAAAT	154214
rs146094214	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125063360	TAAGGTCAACATATT[C/T]ATTATTTCTAGATGA	154214
rs146117555	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125030044	GGGAGGTGAAAGGCA[C/T]TTCTTACATGGCAGC	154214
rs146117802	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125071344	TCACCCGTGCCATCA[C/T]GAGGGTGAACAACTG	154214
rs146137098	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068427	CCTCTGACCCTTACA[C/G]CAGATCAAGCTCATC	154214
rs146159636	snp	A/T	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125031626	TAATTCCCAACAAGT[A/T]TCTCATCTCCATCTG	154214
rs146229003	snp	A/G	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:124988558	GTAATACAGTGAATA[A/G]CCACAACCGTTAAAA	154214
rs146237473	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054755	AAACTTTAGGATGCA[C/T]ACAAATCACCTTCGG	154214
rs146237967	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009684	GTTGTATGATCCCTC[C/T]AAAAACGTAGACAGA	154214
rs146256184	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125052425	GTTTTAGCTGTGCTG[A/T]GAGAAACTAAGGCAA	154214
rs146279077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013596	CTGTTTTCTTTTAGT[A/G]AAGACTTATAGAGTT	154214
rs146289720	snp	C/T	1.65916e-05	0.00288019	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125057968	TACCTGCCAATTCGT[C/T]TGGTGTTTTAAGTGC	154214
rs146358711	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987182	TAGGTGGAAGCTCCT[C/T]AGTTGCACAGTCAAA	154214
rs146398255	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990443	GAGATATCTCAAATT[C/T]GACATCTCAAAAACT	154214
rs146398866	snp	A/C/T	0.000314893	0.012544	intron-variant, missense	RNF217	GRCh38.p7	6:125082554	ATATGCTATACTGCC[A/C/T]GAAACAAGTGTGAGT	154214
rs146412629	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125004141	AAAATCTAAAAGGAA[A/T]TATTAGACAAATGTT	154214
rs146414490	snp	A/G	0.00236305	0.034292	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081497	ACTAGGGGCCATAGC[A/G]GTTGTAATCGGTAAG	154214
rs146433532	snp	A/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125076034	TGAAGCTGTGTTTAC[A/T]TGTAACTTGACTGCA	154214
rs146446749	in-del	-/TTACCTTACCATTGGTAAGTAGCTTTC	0.3744	0.216852	intron-variant	RNF217	GRCh38.p7	6:124989057	TACAATATAATTTAA[-/TTACCTTACCATTGGTAAGTAGCTTTC]TTTGCTTGTCTAACA	154214
rs146454602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010621	GCAATAAAAATAGTT[C/T]GTTGTGTTAAAAAAA	154214
rs146467615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012631	CTATGCAGAATTTTC[A/G]TGAATTTGTTCCTAT	154214
rs146498353	snp	C/T	0.0341408	0.126114	intron-variant	RNF217	GRCh38.p7	6:124965447	GCATGGTGGCGCATG[C/T]CTGTAATCCCAGCTA	154214
rs146538432	snp	A/C	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125059514	TAACAGTTATTCATA[A/C]GTGCATTTTATATCC	154214
rs146542751	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982187	TACTTTCCAACTTGA[C/G]TTTTCCCTTGGCTTA	154214
rs146555313	snp	A/G	1.7808e-05	0.0029839	missense, synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125082885	TTGTATTTCCTATCT[A/G]TTGCCTTTGTAAAAA	154214
rs146556967	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056915	TCCTCCATGTCAAGT[A/G]GAAGACAGATATTCA	154214
rs146620310	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125024644	AGAATCTCTTGAGCC[C/T]GGGAGGCAGAGGTCG	154214
rs146655296	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042660	TGGATGTTGGATGGT[A/G]TCCCGATGTGGTTGA	154214
rs146673902	snp	C/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125039994	GCCCACATCAGAAAG[C/G]TGGAAAGATCTGAAA	154214
rs146696663	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047381	AAATCATGTTGTGAT[A/G]AGCATAATGTATCAC	154214
rs146738928	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002151	GGCTTACTTTGATGA[A/G]CCTAGCCAGGACATC	154214
rs146748778	snp	A/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967537	CACTCTGCCTAAAAG[A/T]GCTAGAGATTGGCAG	154214
rs146775843	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025334	ATGGACAGATGATAA[C/G]GACTGGAGACCAAGG	154214
rs146815714	snp	G/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124978730	TCAGTGAATGAGAGG[G/T]TTACAGCTCATTTGT	154214
rs146847211	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086510	AACTTAATTATGCCA[C/T]TGTGAAAAGTAGGAA	154214
rs146860232	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981957	CACTTGAACCCGGGA[A/G]GCAGAGGTTGCAATG	154214
rs146911965	snp	A/G	0.00953873	0.0683987	intron-variant	RNF217	GRCh38.p7	6:124970741	AGTCCGAGCATACCA[A/G]TGTTCACAAATATGG	154214
rs146944345	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989907	AGACAACAAAACCCC[C/G]CTTGTAGGGCTCCAT	154214
rs146947141	snp	A/G	0.0287284	0.116357	intron-variant	RNF217	GRCh38.p7	6:125065103	ACACGGTGAAACTCC[A/G]TCTCTACTAAAAATA	154214
rs146960783	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125064843	GTGTATGTACGTGTG[-/TA]TATATATATAGTTAG	154214
rs146960787	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984849	CAAAGAATTCCTGCA[C/G]GGGGAAAATGATACT	154214
rs146963356	snp	A/C	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125062538	CAACTTTACTTAGCC[A/C]TTTTTATTTGAATCT	154214
rs147051384	snp	A/G	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125049851	ACTATGTCTGGAAGA[A/G]GAGGAGCAGGTTTGG	154214
rs147067982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044309	CCATGAATATAAAGA[A/G]TTATTGTTCACTACT	154214
rs147123582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011612	GCATCTACTGACATT[A/G]GTGTAGATACATTTT	154214
rs147135002	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125023678	GAAACCACCTAAGTG[C/T]CCATTGATAGATGAG	154214
rs147151586	snp	G/T	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125020155	CTACCATTGCAATTC[G/T]CAGACACCCGCTGGC	154214
rs147155500	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124980074	CAAGCAACGTAGGAT[C/T]AGCCTCTGTTCAACT	154214
rs147220859	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125079382	TTGATTTCTAGATGG[C/T]AAATAATTTATATAA	154214
rs147240116	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125000773	TCATAGTCTAGCAGT[A/G]TGCCGTATTACTGGA	154214
rs147242157	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125077742	GAATTCCTTTTCTGG[C/T]CGTGTTTCTCATGTG	154214
rs147255866	snp	A/G	0.00835141	0.0640778	intron-variant	RNF217	GRCh38.p7	6:124996132	TGCCAGTTGATACTC[A/G]CTCCACAGCTGATGA	154214
rs147258478	snp	A/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125073942	AACTTGACACTTGGG[A/T]GAGGTAAAGTAACTT	154214
rs147346458	snp	A/T	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:124981091	TCAAATTAGATGGTG[A/T]GAGCAGTCACAGACA	154214
rs147348310	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125058293	ACCATGTATATTCTT[A/G]TTTTTGCATTACTCT	154214
rs147362660	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124977225	AAAGTACAAATGTAC[C/T]AGCTGAATTTCAGCC	154214
rs147364826	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125055537	TGACATTTATAGAGC[A/G]AATCCGAGTTTCAAA	154214
rs147426032	in-del	-/C	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967746	TAAATTATGAGTCAT[-/C]CAAATCTTCATGGGT	154214
rs147448620	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981800	GAGGCAGGCAGACCA[C/T]TAGGTCAAGAGATAG	154214
rs147453055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041121	AAGCAATGCATTTAT[C/T]AATTAGCTTGATTAA	154214
rs147456900	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964531	AACTGAACAGGGCTC[C/T]GTACCATGTGATTCC	154214
rs147469054	snp	G/T	0.00953873	0.0683987	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083275	TCTTCTGAGAATTGC[G/T]TGGACTGTCTTTGAA	154214
rs147606766	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074819	TAGCTTATGGCTAAG[A/T]CTTGACTGACAAGAG	154214
rs147711238	snp	A/G	0.0134861	0.0810011	intron-variant	RNF217	GRCh38.p7	6:125011876	AGATAATAACTGCCA[A/G]CCCTAGTTTTTGGTG	154214
rs147726791	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125053674	TCAGGAGAAAATGCC[A/G]TTTTCTTAGGGCAGG	154214
rs147746240	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125015594	TAGTATGTAGAGTAT[A/G]ATCACTATTTTACTT	154214
rs147762287	snp	C/T	3.29881e-05	0.00406115	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076756	TACCGCCAGCTCCGA[C/T]TTTTTGGAGACCACA	154214
rs147814348	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988739	TCTCTAATTAAAGTT[C/G]TTTAATCGTTAACAC	154214
rs147850446	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124992407	AGAAAATAAGAAACT[A/G]AGAGGCTATAGAACA	154214
rs147853324	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125070063	TTTATACCTTTGCAT[C/T]CCCATAGCTTAGCTC	154214
rs147922621	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049732	AGAGAGCAGAATGAG[A/C]AACCCTGGGTATTGA	154214
rs147926288	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124970766	ATATGGAGTCTGGGA[C/T]ATCAGAAAGAAGAAG	154214
rs147938967	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092013	ATTAAACTAAACCAT[A/G]TGCTTAGAAAAGACA	154214
rs147957534	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124973665	TGCAAAAGTAATGGC[A/G]GAAACCCCAATGACT	154214
rs147959098	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125053051	TGTGCTCTTGGGCCT[C/G]TGTGTGGTGGCTCAG	154214
rs148009694	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124989981	TGTTTTGCAAAAGTT[A/G]TCTCCACTCCCATCT	154214
rs148041719	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975686	AAGCGATCTAACCAC[C/T]TGGGCCTCCCGAAGT	154214
rs148079233	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967871	GCAACCTTTGCCTCC[C/T]GGGTTCAAGCGATTC	154214
rs148095638	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125013309	TAAGAGGAAGGGTAG[C/G]AATAGGCCAAAAAGA	154214
rs148133198	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125040422	TGAATAGACCAATAA[C/T]AAGTTCTGAAATTGA	154214
rs148150045	snp	C/T	0.00040006	0.0141375	intron-variant	RNF217	GRCh38.p7	6:125082593	GTGCAAATGATATGA[C/T]TGTGGACAATAAAGA	154214
rs148180755	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125070933	TTTCTTGGTGAAACT[A/G]GAGACAAATACTTGT	154214
rs148219226	snp	C/T	0.00164023	0.0285906	intron-variant	RNF217	GRCh38.p7	6:125058154	ATGTACATCTGGATG[C/T]GACTGAACAATATTT	154214
rs148255373	snp	C/T	0.00993419	0.0697739	intron-variant	RNF217	GRCh38.p7	6:125018362	TATTTCTAGTATTTT[C/T]TTCAGAATTTGGCTT	154214
rs148390965	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124970021	GAGTTTCCAGGAATC[A/G]CAAGGAGATCTGTGA	154214
rs148407239	snp	A/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125015411	CACAAACAAATACAC[A/T]AGGATATTAATCACT	154214
rs148409447	snp	A/G	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090576	CATCCTCTAAGTATC[A/G]GAATGTATTCCATTT	154214
rs148411293	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981472	GTTTGGTTGGGGGGG[C/T]GGTGACTTTCAGGCC	154214
rs148437412	in-del	-/TAGATAGA			intron-variant	RNF217	GRCh38.p7	6:125074298	TAGACAGAAGATAGG[-/TAGATAGA]TAGATAGATAGATAG	154214
rs148443137	snp	A/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965105	TTAGGAAGTTTTAGT[A/G]ATGGTAGTAGGGAGA	154214
rs148444994	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125041478	AAGGCCCATGTGATC[C/T]GTCTTCTGCCTAACT	154214
rs148461244	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083918	TGCTTCACTCTATAG[A/G]TAGATCCTTCACATT	154214
rs148497783	snp	A/G	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125072972	ATAAGGCTTAAAAGT[A/G]CTAATCTGTGTACAA	154214
rs148584941	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030004	TAAGAGTTACACGTG[G/T]CTGGGGAGGCCTCAG	154214
rs148600423	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125010937	TTAAGATGTACCTTC[A/G]AAAAGACGGGGTTGA	154214
rs148617338	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052623	CTTTCCATTGCCACC[A/G]TCTGACTTTAGGATT	154214
rs148652162	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125001496	CGTAATGATATGTTT[C/T]GTCAACTAGTAATTA	154214
rs148701019	snp	C/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125079833	AAATAAAATACGATA[C/T]ATGGATATGATAGCA	154214
rs148705922	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125037965	TGAGGCCTGAGATTT[C/G]TACTTTTTCCCGTCC	154214
rs148755794	snp	A/G	0.00041311	0.0143661	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058045	GAGACAAATTGTTGC[A/G]TCACTGGGCCAGCGA	154214
rs148795419	snp	A/G	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124986288	GTGACCTTGTTTTTT[A/G]GTGATTGTCAGGTTG	154214
rs148797082	snp	A/C/G	0.0471741	0.146251	intron-variant	RNF217	GRCh38.p7	6:125062835	CCCACCTCAGCCTCC[A/C/G]AAAGTGTTGGATTAC	154214
rs148862268	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125075587	TGCCCCCATGATCCA[A/G]TTCCCTCCACTTGAC	154214
rs148897872	snp	G/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125030251	TGAGATTTCAGTGGG[G/T]GCACAGCCAAACCAT	154214
rs148930270	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125053930	GGACAATGTATTTAG[C/T]AAACATCATCTGATA	154214
rs148986134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020809	AACAACAAATAAATA[C/T]TCTAACATATATTAA	154214
rs148999007	in-del	-/ATAG			intron-variant	RNF217	GRCh38.p7	6:125074305	AGATAGGTAGATAGA[-/ATAG]TAGATAGATAGATAG	154214
rs149000705	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961106	TTTGCATCTGATTTG[A/G]AAAATATTTTAGAAC	154214
rs149053998	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124992740	GCAGAACATTCTTTG[C/T]TGTAATGATTTTTTT	154214
rs149107970	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125064322	TTTTTATGGTATGCC[A/C]AGCTCTAGACCTTAG	154214
rs149142643	snp	G/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982436	TTTTCAATATTTATC[G/T]CACTTTCCAGATACT	154214
rs149177742	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125050032	ACTTACGAAAATGAA[A/G]AAAATATTCTTTGGG	154214
rs149194995	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:124978408	CAGGCATGCTGTGAG[C/T]GGCTTCCACCTTGGG	154214
rs149213998	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999040	AGTATAGAGCTTGCA[A/G]TTGATTTATAGCAGT	154214
rs149230532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125043842	TTTGTACAGTAGTAG[C/T]ATAAAATTATGCAAC	154214
rs149246798	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029857	AATTAGCTGAGATGA[C/T]GACAGCACTGTGTAG	154214
rs149332921	snp	A/G	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083672	GATGATGGCTCCTTT[A/G]TGGACATAATTTAGC	154214
rs149335568	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124975244	ACCACAGCTTTTCCC[C/T]CGGTTGCTTAACAAT	154214
rs149367987	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124995129	AGTTATTTATACCAC[C/T]ACCTTCTTCATCCAT	154214
rs149369829	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125072580	CATAAAGATTTTAGA[A/G]CCCAATGAAGCAATA	154214
rs149388632	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125013062	AATTGAAACATACTT[C/G]AAATAATTGACATTT	154214
rs149395532	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074301	ACAGAAGATAGGTAG[A/G]TAGATAGATAGATAG	154214
rs149422572	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066817	AGCACTAAATAATAG[A/C]TAATGGCTGAATAAA	154214
rs149458016	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:124985803	ATCTCTAAGGTTGTA[C/T]TTTTTATATAAAAAA	154214
rs149494817	snp	A/C	0.00103561	0.0227318	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081482	GGTTTTGGGATTGGC[A/C]CTAGGGGCCATAGCG	154214
rs149512223	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125057484	ACCACACCCAGACTG[C/T]TACTGTGTTTTTTAT	154214
rs149516201	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124979724	TGATGGTAAATCTTC[A/G]GACAGTTTGCTTGAG	154214
rs149543950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046454	ACCCGAGAACTTCCA[C/T]GACACACCAGTGCCC	154214
rs149580068	snp	G/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125037626	CTTCCCATAATCACT[G/T]ATGAGTAAAGTGAGG	154214
rs149599133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971345	AGGCTGCCACTCAAA[C/T]TTAGGTCTAGAGATT	154214
rs149631358	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125031557	AAATCTCTAGGGCAG[A/G]GGCAAAAAGCTGCCA	154214
rs149664057	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125055490	TGATAGTTCAGCACT[A/T]AATCACAAAGATCTT	154214
rs149681395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075019	TGTGAATGAATAAAG[A/G]TGTGACTTGAGCAAG	154214
rs149685318	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997730	TTAATCTGCTCGCTC[G/T]CTCTACAGCCCTGAA	154214
rs149699865	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125014693	TTAACATTCTGATAG[C/T]ATGAAAACTTCCTTC	154214
rs149733317	snp	A/G	0.0322114	0.122752	intron-variant	RNF217	GRCh38.p7	6:125069831	TTTTTAATAATACCC[A/G]TTCTGACTGGTGTGA	154214
rs149741519	snp	A/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB, downstream-variant-500B, missense, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964738	AGAGATTCTTAAAAC[A/T]GGAGGAATGTCTGCT	154214
rs149769103	snp	G/T	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124987668	ATTTTTAGAGACAGA[G/T]TCTGGCTATGTTGTC	154214
rs149771052	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125063741	TCTCAAAAGAAAGTT[A/G]TAAACAAGAGGTAAT	154214
rs149823293	snp	A/G	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:125058798	TTGGACTTGATGTCT[A/G]TAGTATAGGGATCTG	154214
rs149855797	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049188	GATGGAGAAATAAAA[A/C]AATGTTGAAGTTTTG	154214
rs149862391	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989635	TATTTGTAAACACTT[A/G]AATTTGATATAATTT	154214
rs149871556	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125016427	CTTTGATGGTATATG[A/G]AATCAATGTAATGGG	154214
rs149917265	snp	G/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124973094	TAAACTATTTGAATA[G/T]ATAGGCAAAGTGATA	154214
rs149928161	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124992485	TCTAATGCTGTGTAG[A/T]TGTAATGGCTGTTCT	154214
rs149949183	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125001409	CGGTAGAATGAAGGA[A/G]CTAGTGAAGTCTGGG	154214
rs150032644	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125024625	CGGGAGGCTGAGGCA[C/T]GAGAGAATCTCTTGA	154214
rs150066492	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085338	GGTTTTTCATTTTTC[C/T]ATTGAGTAGATATTT	154214
rs150068870	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124978331	CGGCAGGCTGCATTC[C/T]GCTTGTGCCCCAGAC	154214
rs150082835	snp	C/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125066479	CCCTTCTCAGGATCT[C/G]AGACTTGCCTTGTCC	154214
rs150087551	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990108	TTTATCACTCTATCC[G/T]CCTTGAAATACTTTC	154214
rs150134896	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125060787	ATCAAGGTGATATAA[C/T]ATCAGATAGAAATTT	154214
rs150171491	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125021668	TATATGAAAATGTTG[A/G]TATTGGTAGTATTAG	154214
rs150223551	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125053904	TCATAGTGCTTAGTA[A/G]AAGTTCATTAGGACA	154214
rs150227522	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974067	AGGCTGGCCTCCCCC[A/G]GAGCCAGCATCCCAA	154214
rs150255313	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125040760	TCAAGTCGGCTTCAT[A/C]CCTGGGATGCAAGAC	154214
rs150258183	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125004789	GTCTCACTACTTTAT[A/G]TTAATAATTACACAA	154214
rs150291356	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125031034	TTTGCACATGCACGC[A/G]GAACACCACATGGAA	154214
rs150295485	in-del	-/T	0.0700422	0.173537	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087988	ATGATACTGTCCCCC[-/T]AATATGGAAAATAAG	154214
rs150304563	snp	A/G	0.000167723	0.00915607	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125081455	AAAATTATTCATTGC[A/G]CCTCTAATTATGGTT	154214
rs150349938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027301	TACCTCCCCGCCAAT[A/G]CCCAACTACCCTTCC	154214
rs150416403	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124971088	AGGGAACTCGAGGTT[A/G]GAGAGATTAAATAAC	154214
rs150432915	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016861	GGGTGCAGCAAACGG[C/T]CATGGCACGCGTATA	154214
rs150467514	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125077203	TATCCAGCAGCAGGT[C/T]GTACACATATCCTCC	154214
rs150476150	snp	C/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967020	AGTTTCTGATCGCCA[C/T]GGTGAAGAGGTGAGC	154214
rs150536655	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055075	GAATATGGTTAAGTT[C/G]AAAATGAATGAGGCA	154214
rs150578355	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125009125	AATGTATGTATAAAG[A/G]GATTTGTTCTTTGAC	154214
rs150625951	snp	G/T	0.000399281	0.0141238	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045382	CCTCAGTGCAAGCAC[G/T]TTACAACCTTCAAGA	154214
rs150661202	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124994075	GGTCATGATGGAAGG[A/G]AGAGGAAAAAGCAAG	154214
rs150679432	snp	A/G	0.00013235	0.00813371	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045341	TCTTGGAACTTGGCC[A/G]TATTGATTCCAGCAC	154214
rs150694278	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125058731	TAGCCAAGCAAACAG[C/T]CAGGGAAGACTCTCC	154214
rs150751254	snp	A/T	0.0174175	0.0916809	intron-variant	RNF217	GRCh38.p7	6:125018831	ACTGGAGGTGTGCAC[A/T]GGAGGTACTGCAGTG	154214
rs150787221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969311	TTATATAAAGAAAAC[A/G]CAATTTTGCTCAGTT	154214
rs150798998	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089249	CCAAGCTTCAGAAAT[C/T]GCTTCGTGACTGTTG	154214
rs150815493	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068952	GAGGAGAGGTGAAGA[C/T]GAAGCTGAAGGAGGG	154214
rs150839783	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124999814	ATCCAGTTGTACTTT[C/T]CACATACTTTATACT	154214
rs150867973	snp	C/T	0.0221141	0.102801	intron-variant	RNF217	GRCh38.p7	6:125063057	TAGTCATTACAAAAC[C/T]AAGTCTAGTTCGTAA	154214
rs150905090	snp	C/T	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:125024362	CTGAGGCAGGCGGAT[C/T]ACCTGAGCTCAGGAG	154214
rs150942659	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970382	ATATTGTGAAGTTAG[A/G]ACTGACAGAATGCCA	154214
rs150980466	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124997396	CATTCCTACCCTAGG[G/T]CTCTGCCAATTACTT	154214
rs150986062	snp	A/G	9.93032e-05	0.00704569	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058067	GGCCAGCGAAATTGA[A/G]CATGGGCAGAGGAAT	154214
rs150996125	snp	C/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125041521	CTCATACTGTTCTCT[C/G]CCTCCTTTAGTATAT	154214
rs151011168	snp	G/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983148	TATTGTCTTCAGAAG[G/T]GTCATAAATGCTCAG	154214
rs151069305	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124987414	CCCCATCCTAAGAAA[C/T]CATGAATCTAGTTTC	154214
rs151102170	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124973985	GTCAGTGAGCTCAGC[G/T]ATGGCTGTCTACCGA	154214
rs151113329	snp	A/G	0.0146672	0.084371	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090870	TTCATTAGTTATACT[A/G]TTAACTTTGATAATC	154214
rs151138311	snp	A/G	0.00358779	0.0422022	intron-variant, missense, nc-transcript-variant	RNF217	GRCh38.p7	6:124966739	TCTTTGAAAGAAGAT[A/G]TCAACTTGGAAGATA	154214
rs151151197	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084850	TTTAACAGATATTTA[C/T]TGAGTGCCTATCTTA	154214
rs151154984	snp	G/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125011379	TATCATATTCACCTG[G/T]AAAATCAGAAACTGA	154214
rs151186494	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125039282	CAGGATACATGTACC[A/G]AAGCAAGGGTTGCAA	154214
rs151188618	snp	A/G	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125064912	ACATATTTTGGACTT[A/G]CATATAAAGTAGAAT	154214
rs151202787	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125080857	CTTGAGTAACTTTCA[A/G]CGTACTAGGTATTTA	154214
rs151243798	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124991664	ATTTGTTTTAAATAG[C/T]ATCTTGAAGACAATT	154214
rs151277546	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125056444	ATCTTTTAAGCCTTA[C/T]GACAGAATACCATTT	154214
rs151280357	in-del	-/GAG	0.150667	0.229419	cds-indel, nc-transcript-variant	RNF217	GRCh38.p7	6:125086335	ATAAAAATAAAATTT[-/GAG]GAGATGTGTGTCAGA	154214
rs180780685	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091071	TTTCTTACACTTTTT[A/G]GAGCAATCAACTTAT	154214
rs180800655	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079568	CTCAAAATGAGATAC[G/T]TTGAGTATTATTAAC	154214
rs180804427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036930	ATTATAAAGCAGGAA[A/G]TAACAGATGGAGAGG	154214
rs180810337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071400	GCATTTTTTGGATAT[C/T]GTGTTTTGTTTTTTC	154214
rs180816351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125043164	GCTGTTCATCTTTAA[A/G]AGCCGTCCCAAGGCT	154214
rs180832792	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054121	GGAGTGAACTTGTGG[A/G]CTGTTGGAGAGATTA	154214
rs180843401	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006514	TTAGATTTATTTAAC[A/T]TACATTTTCAAATTT	154214
rs180843838	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125017888	AACATAGCATTGCCA[A/T]TACTAAGGGAAAGAA	154214
rs180851875	snp	G/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125064791	ATATCACATGTCATC[G/T]ATACTTGTATGTATA	154214
rs180852739	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124970812	GGAGTGGGCTAATTC[A/G]GCAAGAAGAGTACTG	154214
rs180853223	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979784	GATTCTAGCTTCTGT[G/T]TGGAGAATGAATTGT	154214
rs180853503	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998499	AATATTGGTCATAAC[A/G]TTTAAAAACTGTGTA	154214
rs180862274	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026702	AGCTTTTTTTAGGTA[C/G]GGAAGGTTGCATATT	154214
rs180867503	snp	C/T	0.000798403	0.0199641	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963249	GCCCGAGCCGTTCTC[C/T]ATGCCCAGCCTGTTG	154214
rs180891985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986964	AAATATTCATCTGTC[A/G]TACTGATCTGTGTTG	154214
rs180959652	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975892	TCAGTGTTTTAATTT[C/T]CCTGTTATCATTTTT	154214
rs180963344	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125001435	CTGGGGCACAGAGAA[C/T]CCCGTATTAATGTTA	154214
rs180972837	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021728	CATTTTTCTGTTTTC[A/C]CAGTTTCCTTTATAA	154214
rs180975975	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982586	AGTAACACATTTTAC[A/G]TAATAACTTATAATC	154214
rs181004048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966440	AGTGCTTTCTTTCTC[A/G]TCTTAAAAGGTCTCT	154214
rs181150991	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085288	AGTGATGGCTATTTC[A/G]TCAGTGCTTGAAATA	154214
rs181151420	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125048590	GTCATTCTTTGAACA[C/T]TTATTATGGCTTTTG	154214
rs181154052	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125059973	CTGTCTGTTTAAGTC[A/G]TATTTTATGATGTGT	154214
rs181164388	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125068460	TTGAGTACTGTCTTC[A/G]TACTTTCTACTTTTC	154214
rs181165353	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074846	AGAGTCAAACAACTA[C/T]TGAAGGATTTGACAC	154214
rs181165448	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039106	ACATGTGATGTTTGG[G/T]TTTCTGTTCCTGCTT	154214
rs181171871	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031413	TTTCCAAACATTTAC[A/G]CTGTTTCCCTTTTAA	154214
rs181179855	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:124993896	AGCAGGAGATCCTCT[A/G]GAGAGGTGAGTGGGA	154214
rs181184876	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125013787	CACAAGATTTTTAGT[C/G]TAGCAGATCTATTTC	154214
rs181204077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028202	CAGATATAGTTTGTT[A/G]GTTTATCTTAATCCC	154214
rs181211768	snp	C/T	0.000307892	0.0124037	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045418	GGACATATTCCCACC[C/T]CTTCCAGATCAGAAA	154214
rs181215489	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125007672	CATGTTTTCTTGTTC[C/T]TAACTGTGGTTTGCA	154214
rs181289395	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090702	GATTGCATATTTTTA[A/G]TTTTCTATAAAATTT	154214
rs181294284	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125053484	TGCTACTTTACACAT[A/G]GATGTTGTCTAATAT	154214
rs181302421	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017112	TGAGTACAACTTAAA[A/T]TTTTTAAAAAGACAT	154214
rs181310930	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988140	GCACATGCGAGGGAT[C/G]TGGGTTGCACGCTCC	154214
rs181321350	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124979604	AGGAGGCAATGAGGT[C/T]GCAGCAGCACAGAGA	154214
rs181325835	snp	A/C	0.0166325	0.0896639	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962047	CCTCTCCCCCAGGGG[A/C]CCTGCGGCTGGCCAG	154214
rs181357626	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065587	GCTGTGTTATAGATG[A/T]TGAGGGCTTCTGCAA	154214
rs181360612	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125080575	GCATTTGAGTTGTGC[A/G]GCCCTGAAGCTGTGT	154214
rs181391451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071127	AAACAACTTGAGGAG[A/G]ACAGGTACTATTTTC	154214
rs181403256	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125036553	AAAGAGCTTCTGCAC[A/G]GCAAAAGAAACTATC	154214
rs181404710	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124997924	CTGTCCTTACCTGTT[C/T]TTATGTGACGGTGAC	154214
rs181408201	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124972312	CTGTCATTTCCCTCT[C/T]TCAGGCCTCTACCAT	154214
rs181479516	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068064	GTCATGGATAATATT[A/C]ATGTGTTTTTTTAAA	154214
rs181488977	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125023254	TAGAACAAAAGCATG[C/T]GGAGGAGCCCAGAGG	154214
rs181513562	snp	A/T	0.0123036	0.0774623	intron-variant	RNF217	GRCh38.p7	6:125048466	ATTTAACGTCTCTTT[A/T]TAATAATGTTTACAG	154214
rs181618367	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124987835	CTTGTGATTCAAATA[A/T]TAGTTGTTACAATGA	154214
rs181628333	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007033	TGTTACAGTAATTAT[C/T]AAGTATGTAAATAAA	154214
rs181630951	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971712	TCCTGCCTCGGCCTC[C/T]CGAAGTGCTGAGATT	154214
rs181640714	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076910	GAATTAAGTAGTGAA[A/G]ATAGAACTTGGAAAT	154214
rs181667676	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125039908	AAACCAGTAAGGACA[A/G]AGAGACAACATACCA	154214
rs181702064	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125012622	AAATTTATTCTATGC[A/G]GAATTTTCATGAATT	154214
rs181710422	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124975243	CACCACAGCTTTTCC[A/C]CCGGTTGCTTAACAA	154214
rs181772984	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125061594	CATTTTCCCTGTTTT[C/T]TATTTCTTCCTTTTT	154214
rs181785601	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125044541	TACATTAATTTTGTA[A/T]ATTACCGCAGTAGCA	154214
rs181793414	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	RNF217	GRCh38.p7	6:125093087	ACCAAAGGGTAAGTA[A/C]AAGAATTTTCCTTAA	154214
rs181796786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027044	GTACATAGTAGGTGT[A/G]TATATTTATGGAATA	154214
rs181853092	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993538	TTCTAGTTGTGGCAC[G/T]CACTATTCCAGATCT	154214
rs181859596	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961761	TTACTAATTCCAGAG[C/G]TGAGTGTAGTTTTGT	154214
rs181906620	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125012351	CATTTACTGATGAAT[C/T]TGAGATATGTACAAT	154214
rs181910411	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992582	AGAATAGTGAGAAGA[A/G]GGGAGGTTTTTCTTG	154214
rs181923406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974672	TCTTTGTTAATGAAA[A/G]GAGTTCATGTAACAG	154214
rs181968704	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125065072	CGAGGTCAGGAGATC[A/G]AGATCATCCTGGCTA	154214
rs182080519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076595	TTTCATAAAATTTGC[A/G]ATTTTGCTTTTTAAA	154214
rs182120109	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125038227	TTCAGTGATATAAAT[A/T]GTTGTATTAGCATTT	154214
rs182132826	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125060304	ATATAAATGCTTTCA[A/G]TCATGATAACTAAAT	154214
rs182139010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020776	ACACATGCCTAGAAC[A/G]TTCACAGAAGAGGGG	154214
rs182142992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022121	CTCCTTACCTTAGGT[A/G]ACCACCTACCTTGGC	154214
rs182145045	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125000177	AAATAGTATTAATAG[C/T]ATAAAACCTTGCCAC	154214
rs182147607	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124980391	CCTCCCCTTCCCAGA[A/T]ATAACAAAGGTCTTA	154214
rs182170437	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983135	CTATTTATTTATTTA[C/T]TGTCTTCAGAAGGGT	154214
rs182240386	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079990	GTTTATTTCCTATCT[C/T]GTTCCTTCAATTCTG	154214
rs182266037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072750	ATATACCTTGTGGAG[A/G]GAGAGCTGACATGTT	154214
rs182273300	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057637	TGGATTTGGGGCCTT[G/T]TGAGCCTTCAGGTTC	154214
rs182385813	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125077475	TGACTTTTTACCCCC[G/T]CTTCCTCAACAACAC	154214
rs182394935	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125062625	CTTTTCACCCGGGAT[A/G]GAGTGCAGTGGTGCT	154214
rs182403040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994738	CTACTTTAGGCAGTT[A/G]TATGGCATTATATTT	154214
rs182410657	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040115	ATTGAAGGAGATAGA[C/G]ACATGAAAAAACCTT	154214
rs182417527	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004646	GTGCTGTGAAGGCCT[A/G]AGTCTTTTTAAATGA	154214
rs182418104	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039224	CATGGTGCATATGTA[A/C]CACATTTTTTTTTCT	154214
rs182419155	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024645	GAATCTCTTGAGCCC[A/G]GGAGGCAGAGGTCGC	154214
rs182419529	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125003538	ACTTTAGAGATTCAC[A/T]GCACAGTATGGTGAC	154214
rs182435602	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966984	TAGTGGAATAACTTT[A/G]CAGTGCAGTAGCTGC	154214
rs182488377	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045720	GAGTAATAATAGTTA[C/G]TACTACCAAATACTA	154214
rs182491570	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125081281	TATATCTGTTCTATA[A/C]CTAATCCTGATACAT	154214
rs182522979	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125008830	TTTAATACTTTTATG[C/T]GTGTGTAGCTGGTGG	154214
rs182535856	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972617	AAATTTTTTTCTTCT[C/T]TGAATGCTCCGTGAC	154214
rs182536443	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124999875	ATTAAACTATTAAAT[A/T]AATATATGAAAAAGG	154214
rs182539794	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124979987	TTTAGTATAGCAGAA[C/T]GTCCTTGCAGCCTTT	154214
rs182541828	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964386	ATTATCTTACATGCA[C/G]TGAAGTTGTTTCTTT	154214
rs182701370	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125018920	GTGGTAAGTCTCCCC[A/G]GACTCCATTTGGCCA	154214
rs182756085	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125065906	TCAACATCTTCAACC[A/G]GATCTAATAGACTTC	154214
rs182761549	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125028808	TACTGTGTTAAATTA[A/C]TGTGATGTGTTCCAC	154214
rs182770500	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964549	ACCATGTGATTCCTC[A/T]ATGTTTTTTGGCTAA	154214
rs182774729	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124989345	TTGTGCCTTCAAAGC[A/C]TGACACTTGAAGTTT	154214
rs182783964	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125069679	TAATAGGACTCCTGG[A/G]TCCAACTGTAGTTCT	154214
rs182796221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082063	CTCAGACTCTAGCAT[A/G]CTTTAGAATATCCTC	154214
rs182818022	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125035822	GGTTTGAGTTAAAAG[A/T]CAAGACTTATTTGTG	154214
rs182820339	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125066681	TTTTTTCTCCATGGT[A/G]TTATATTACTTATCA	154214
rs182826217	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125046807	AGTCAAAGCTTCTTC[A/C]TGAGTCGTTGTTCTT	154214
rs182847434	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984050	GCCCTCCATCACCTC[C/T]CAAAAGCCCCACTTC	154214
rs182853369	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004097	CATCCATCAAATAAG[A/G]TTGCCTTTCTTAGAG	154214
rs182859274	snp	G/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124968738	TTCCCTCCTAGAGCT[G/T]TTATACCTGAAGGCT	154214
rs182866041	snp	C/T	0.00358779	0.0422022	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967996	TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGACC	154214
rs182948705	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125050209	TCCCCCTTTTCATAT[C/T]GATTTGGAGAAAGAG	154214
rs182958318	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068893	GTAGAGGGCCAGGTG[G/T]AATGAAAGGAAGGAT	154214
rs183064215	snp	A/G	0.00716266	0.059414	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088611	TGTTACAAACTATAT[A/G]TATCTTTTTGGCTAG	154214
rs183101186	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050701	TGTAATGAGTATGCT[C/G]CTTTGTTCTGGTTTT	154214
rs183114734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015816	CTGTACTATTTCTAA[A/G]AACTAACATTTGGAA	154214
rs183148995	snp	C/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:124984423	TGTGGTGGTGCATGC[C/T]TGTAGTCCCAGCTAC	154214
rs183212043	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125055683	TGAATAATGTCCAAT[A/G]GAAGATAACCGAATT	154214
rs183231633	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066299	TCAAAATTGTCTGTG[A/G/T]TTCCTATCTGACACA	154214
rs183253053	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046474	CACCAGTGCCCCAGG[C/T]CCACCCCAGAACAAT	154214
rs183261887	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125010172	CATTATGCTCGTTCA[C/G]TATTTTGCTCTAAAG	154214
rs183264849	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029801	TGGAATAAAAAAAAA[A/T]TTTTGAAATCAGCTA	154214
rs183265823	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989949	GCTAGTGTTCCTCTT[G/T]TGTGCTTTCTTTATA	154214
rs183276468	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124973169	CTGTAAGACCTCCTC[A/G]TTGCTTCACATAGAG	154214
rs183362499	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125015666	ATTGCTACATCCAGT[A/G]TATTTTCTCTATTTT	154214
rs183371230	snp	C/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125014243	TACCACCATAGAGTA[C/G]ATGGGAAGAGATTTT	154214
rs183375586	snp	A/C	0.00914312	0.0669923	intron-variant	RNF217	GRCh38.p7	6:124976750	CCTCAAGTGATCCAC[A/C]TGCCTGGGCCTCCCA	154214
rs183390493	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994216	TATAGGCAGAATAGT[C/G]TAACCCCATGTGCCT	154214
rs183396193	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124976480	TCACTATGTTGGCCA[A/G]GCTGCTCTCAAACTC	154214
rs183425530	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072401	ATGTACAAGGTTACT[A/C]TAGAGCTTACAATTT	154214
rs183439623	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037728	CTGGAGCTGTGCTTT[C/G]CTTGTAGTAGATCTA	154214
rs183541067	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964152	GAGAGTGCACCAGAC[C/T]AGCTTTCCTTCACTG	154214
rs183544774	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124991801	TCAAATGTAAATTAA[A/C]ATTAAGTAAAGATTT	154214
rs183558210	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125031892	TCACACTTTTGACAA[A/G]GACATACACAAGACT	154214
rs183560301	snp	G/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124974388	AAATAACTTTGGTGG[G/T]GTGTTTTTTGTGCTT	154214
rs183567808	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068666	TAATGTCTGTATACA[A/T]GTATAAGCTCTTTAA	154214
rs183568731	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049246	ATAGACACATCACCC[A/G]CACCCAAAGCTTTTC	154214
rs183582416	snp	C/T	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125033209	GTTCTTTTTTTTTTT[C/T]TATACTTAAGTTTTA	154214
rs183592846	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124994621	TTAGTTACTAGCATG[A/G]TGTTAGGTAGATACA	154214
rs183713733	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037380	TACTTGGGAATATGC[A/C]TTTTTCTCTGGTTGC	154214
rs183721954	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999053	CAGTTGATTTATAGC[A/T]GTATTTGACATAAAA	154214
rs183845462	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125060082	ATTATGTTTTGCCCC[A/G]TGGAACATTTCTATT	154214
rs183854116	snp	A/C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125075406	ATTGACTCATGGTTC[A/C/T]GCATGCCTGGGGAGG	154214
rs183859969	snp	A/C	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124978033	GATACAAACATTAAA[A/C]AAATACTGAGCACAA	154214
rs183860361	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125039135	TTTAGTTTGCTGAGG[A/T]TAATAGCTTCCAGCT	154214
rs183871542	snp	A/C	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125021854	TAAGAACAGCCATTC[A/C]CAGGATTGTCATTAA	154214
rs183887605	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984753	TTCTGATGTCTGTAT[A/C]ACCTTAGTATGGAAA	154214
rs183896293	snp	A/G	0.000293328	0.0121069	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081550	TAGAATTATCTGAGG[A/G]CCATAGAGAGAATAC	154214
rs183907667	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054648	GCAGCTTGCCAACTA[A/G]TGGATACATGTTTTT	154214
rs183941147	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979949	GGATCTTTGCCTTTA[A/G]AAAGTGTTGGAAGTG	154214
rs183977775	snp	A/C	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125064663	TTTGTGCATGCATTT[A/C]GATTTAAGAAACCTT	154214
rs183986141	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125026251	GTGACACAGTGGCAA[C/T]GTGTCCAGGCTCTGC	154214
rs183989458	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125042924	TCACAGAAATGTACT[C/G]CTTCCCAATAACAAG	154214
rs184058460	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124969795	TATTAGAAGATAATA[A/C]GGGCAATGGAGAAGG	154214
rs184066281	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086479	ATCCACTTTTGTGTA[C/T]GTTGCTTGACAGAGG	154214
rs184072970	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125063111	CAAGTAGGCAATCTA[A/G]ATTTTGTTGGAGGTA	154214
rs184075064	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125025529	CGAGGAGGGAGGGAG[A/G]AAGGGATATTTCCAA	154214
rs184155395	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125079156	GAGATCAGAGGTTCT[A/G]CTCATAAATTATAAA	154214
rs184222167	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125077883	GTTGTGAACCATTTT[C/T]CTCCTTAGAAGCATA	154214
rs184223008	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012228	ATAGCATATACAATA[C/T]TAAAAATGAAAGCAT	154214
rs184235975	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040964	TAATAAGAGCTGTTT[A/T]TGACAAACCCATAGC	154214
rs184245512	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125004847	AAAAGGAAATAAAGG[C/T]ACTTTCTAAAGGCCT	154214
rs184295176	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038902	AGGTAAACGTGTGCC[A/G]TGGTGGTTTGCTGCA	154214
rs184310039	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021195	GTGGAGTTTAACTGT[C/G]GTTCCTCTACTCTCT	154214
rs184322423	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982241	TATTTTCCTTTCACA[C/G]TCATATTCATCTTTC	154214
rs184322678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001112	TTTGATTTTTCTATT[A/G]ATTAATACCACCTAC	154214
rs184334297	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966245	ATCTGTGTCAATTCT[A/G]TGGTCCCTCTACTCA	154214
rs184381523	snp	A/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:125071045	GTAGAACCTTGTTTG[A/T]AAATAAAAGGCCACA	154214
rs184425837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047302	TGGGTAAAGGAGTTA[C/T]AATTTAAGTCACAAT	154214
rs184448401	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025883	GATTTTTATTCTGTC[A/G]AGTACAAGGTGAAGT	154214
rs184452440	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124986136	GGAGTATAATTCAGA[C/T]TGCATTCCTCAATTA	154214
rs184457862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005376	TGTTGACTCTGCAAC[C/T]TAAAGACAAATATGG	154214
rs184461254	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970273	GAAGTAAAAAGATCA[C/G]TTAGAAGACTATGGA	154214
rs184518549	snp	C/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125030828	GCCCTCTTCTTGCAG[C/G]TCCACTAGACGGTGC	154214
rs184524595	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125048139	CATGCCCATACCTGT[C/G]TGGGTATTATAGGTA	154214
rs184529429	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125012381	TGGATACTTTAAAGG[C/T]ACTCCGTCATGTCTA	154214
rs184536707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067423	AGAAAAATAATGACA[A/G]TATGAACTAGGCCAG	154214
rs184551460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992645	TGTGGATTTGATCTT[A/G]GAAAGTATGGTACTA	154214
rs184557033	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974699	ACAGATTATTTTTGT[A/G]GTCTAGATATATTCT	154214
rs184572971	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006326	AGTTGTTCAATGCAG[G/T]TGATTAATAATACTC	154214
rs184574582	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125030633	CAGGTCTCATATCCA[A/G]GTCACGCTGATGCAA	154214
rs184601198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970754	CAATGTTCACAAATA[C/T]GGAGTCTGGGACATC	154214
rs184624588	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042035	TTGATGAAATACATA[C/T]CTTGTTGAACACATG	154214
rs184691711	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125067825	ATTCGAATGTGGAAG[C/T]GATCACTCAAGGAGC	154214
rs184708302	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083392	GAAGATAAGAGTTCA[C/T]TGAATGCACCTATTA	154214
rs184729329	snp	A/C	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124986557	AATCATTTCAAATAG[A/C]CTTTTTAAAAGTTGA	154214
rs184815690	snp	G/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125070139	GTTACTTCACTTAGA[G/T]TAATGGCCTCCAGCT	154214
rs184826395	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089148	TCTTGATAGGAGTTG[G/T]AGAACACTGCCTAGC	154214
rs184833300	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125036087	CCCTTGCCCCCTACC[C/T]CCTGACAGGCCTCGG	154214
rs184844884	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125051051	TCTTCAGTTACTAAT[A/G]GAGTGTTTTGCTAAG	154214
rs184847288	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090718	TTTTCTATAAAATTT[A/G]CAGCCATTTTCCAAA	154214
rs184853655	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125016068	CTAATGACACTGGAT[A/G]CCAACTAGAAGAAGA	154214
rs184860610	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124978318	CACCTGCTTAGCCCG[C/G]CAGGCTGCATTCCGC	154214
rs184863905	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995705	GGTGGGTGGATCACC[G/T]GAGGTCAGGAGTTCG	154214
rs184923751	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125058529	CTGACATTGCTGATC[A/T]CTTAAAAATTACATT	154214
rs184938702	snp	G/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125030208	CCCTCCCACAACACG[G/T]AGGAATTCTGAGAGA	154214
rs184970284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990962	TAGTCCTAGCTACCC[A/G]AGAGGGAGGTGGGAA	154214
rs185027106	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074317	TAGATAGATAGATAG[A/G]TAGATAGATAGATAG	154214
rs185070157	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125011205	AATAATTTTAACCTT[C/T]AGGGACAGTAGAAAG	154214
rs185079872	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973967	CAGCTGATGCCGGCC[A/G]TTGTCAGTGAGCTCA	154214
rs185082971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979212	CTCTTGTTATTATCA[A/G]TTGTGTGATGCTGAT	154214
rs185197963	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092782	AACAGAAATTCAAGG[A/G]TGTGCTTTTGGGAAG	154214
rs185202348	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961775	GCTGAGTGTAGTTTT[C/G]TAGGAAGTTCTACTG	154214
rs185236487	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125051891	AGAATTTTCCAGTAC[C/T]CTTTGTGTTCACCAG	154214
rs185258477	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078201	GTTAAACAGATATTG[G/T]AGGGATAACTAGGGA	154214
rs185265197	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125016956	TGGAAATTAGAATCA[A/G]TAAGGAAGTGTATAA	154214
rs185359774	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125063642	ATCATCACTATTAAG[G/T]GATTTGATAAAACTT	154214
rs185367270	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013910	ATTAATTTATGAAAT[A/G]TGTTAACATAAATCC	154214
rs185367800	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036249	TGTCCCTGCAAAGGA[C/T]GTGAACTCATTCTTT	154214
rs185375266	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994129	AATATTAGCCTAGAG[A/G]AAAAAAAATATGTAT	154214
rs185376107	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997682	GTGGCGATGAGATAC[C/T]TGGACACTAGTTTCA	154214
rs185389065	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125073673	CACACTTGCCTATCT[A/G]GGAAAGCACTCTCTA	154214
rs185389187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976114	CATAGACATATGTAT[A/G]CATACTGTTTGTCAA	154214
rs185402521	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038376	AGATATATGGTATCA[C/T]GGTTATGGTTTTAAA	154214
rs185402801	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125000648	TTGTATGCATATTAG[A/G]GAAATAGAGACCCTA	154214
rs185425461	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF217, RNF217-AS1	GRCh38.p7	6:124964906	AAGGTAGCATGGGAT[A/G]AGATGTCAATAGAGT	154214
rs185441118	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065638	ATGTAGACAAGAAAT[C/T]GAGTAAAAAGCTGCC	154214
rs185442825	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080630	AATAACAACATGTAT[A/T]TACTAACCTCTTTTT	154214
rs185457593	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045535	CATTAAGGGGGCATC[C/T]TTCCTTTATGGAGCT	154214
rs185505982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058166	ATGTGACTGAACAAT[A/G]TTTACATTATTGAAG	154214
rs185507752	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125017602	TTCACATTTCTCTGC[A/C]CTTGATACTAGGATT	154214
rs185517795	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125021121	ACAGAATGAACTTTA[C/T]GCAAAAGTTATTCAT	154214
rs185531125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998265	GATTCACCTTGTATG[C/T]CATTTACATTTGCCT	154214
rs185536997	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979680	AGATAGTATAGATCC[A/T]CCATGGAAATTATAC	154214
rs185539044	snp	A/G	0.000409851	0.0143093	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962774	GCCTGGGGCCCCCGG[A/G]CTGGAGTAAGAGCCG	154214
rs185539830	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981366	CCCAGGAGGTCCTGA[C/T]AATAAGTGTGTCCAA	154214
rs185574004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068274	CAGGGCTAGTGCAGG[A/G]TGCTTCTCAATTAGT	154214
rs185577817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040017	ATCTGAAATCAACAC[C/T]CTAACATCACAACTG	154214
rs185592178	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084575	TTTTTGTTGGGCTCC[A/G]GAGTGTAAGAATATT	154214
rs185594477	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023922	TACCAGGGGATGGGC[A/T]TGGGGGGAAAAGGAC	154214
rs185600236	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984103	TTACATGAATTTTAG[A/G]GAGAAGCAAACATTC	154214
rs185602686	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125004113	TTGCCTTTCTTAGAG[A/G]CAGCTTTGAAATAAA	154214
rs185609521	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968200	TATAGAACCTGTCAT[A/G]CCCGGTGTGGTTTTG	154214
rs185688692	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125064867	ATAGTTAGGGTACTA[A/G]AAAATGTAGTGTACC	154214
rs185694850	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125026772	GTGACTCTTGACCCT[A/G]TGGAAGACAAGTGGG	154214
rs185708015	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124987185	GTGGAAGCTCCTCAG[C/T]TGCACAGTCAAATGG	154214
rs185751513	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961089	TAGTCACCTTTGTAT[A/C]ATTTGCATCTGATTT	154214
rs185757230	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125062127	CTGGTGAGTTTTAAA[C/T]GATTATGCCTTTGTT	154214
rs185790612	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079648	ATACTTAATATTGGA[C/T]TTTCATACTTAATGA	154214
rs185811459	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125043820	TTAAATCCTCTCTGG[A/G]CCATGTTTTGTACAG	154214
rs185846923	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006976	AAAGAATGCATGATA[A/G]ACATCTTTGTGTATA	154214
rs185854089	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065929	TAGACTTCTCCAACG[C/T]AGTATGTTCTCTTCT	154214
rs185907842	snp	G/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125065220	GGCTTGAACCCAGGA[G/T]GCAGAGGTTGCAGTG	154214
rs185923475	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125044794	AAGTATTCTGCAGTG[A/T]TGTTGAAAAATGTGA	154214
rs185931455	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007083	GAGATTTGTTATCCA[C/G]TTCACAAATTTTGTC	154214
rs185937977	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027372	GTTCAATTGATGTGA[G/T]TTTTAGATCCCAGAA	154214
rs185941138	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987882	ACTTGTACATTCTGC[A/G]GTTTGTTGTGATTTT	154214
rs185953095	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971733	TGCTGAGATTACAGG[A/C]GTGAGCCACGGCACC	154214
rs185975247	snp	A/G	1.9245e-05	0.00310196	intron-variant	RNF217	GRCh38.p7	6:125081391	GTAATTATTTGGTAG[A/G]TTAGTTTTAAGACTC	154214
rs185988690	snp	C/G	0.00119737	0.0244387	intron-variant, missense, nc-transcript-variant	RNF217	GRCh38.p7	6:124966729	GATGCACAGTTCTTT[C/G]AAAGAAGATGTCAAC	154214
rs185996589	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125048686	AGTTTGAGACCTAAA[A/G]TATCATATATGGGGG	154214
rs186041587	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982989	AGGGAAAGAAAAGGG[A/G]AGAAGCACATATAGG	154214
rs186132830	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125068564	AGCTCCTTAAGGGCA[A/G]GAGCCATGTCAGACT	154214
rs186147666	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125031555	ACAAATCTCTAGGGC[A/G]GGGGCAAAAAGCTGC	154214
rs186160272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972464	GCACTCTCCTTCTTA[A/G]CCTTTCAACACCTGC	154214
rs186162726	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036709	GTGGATGAAGGATAT[A/G]AACAGACACTTCTCA	154214
rs186163898	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125001713	TATAGGATTTCTCCC[A/T]TGTGTGATAGGAACA	154214
rs186304317	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124988315	CTATGGCAGTTTTTC[A/G]TATTCTGAAAAGTTT	154214
rs186344357	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125071239	AAAGTAACATGCGTT[C/T]GGTAGAAACCATATT	154214
rs186346447	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125008709	CTCAGCCCCAGCTTG[A/T]ATCTATCTGGTCCTT	154214
rs186387197	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086660	TAAGAAGAGAGGGGT[A/C]AAACCTTTTGGTACA	154214
rs186412383	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032291	GAAACTGAGACTAGC[A/G]AATGTATTCAGAAAC	154214
rs186415339	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125068686	AAGCTCTTTAAAGGC[A/T]GGAGCCCTGTCAGAT	154214
rs186418544	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049296	GGGATTTTATGATAT[A/G]TATGTGTGGTTATTT	154214
rs186421702	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014332	CTGTACTCTAAATGC[C/G]TTGCATGGATTAGCT	154214
rs186490139	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125031181	CACCCTGGGGACTGT[G/T]GGCCCAGCCCACGAA	154214
rs186508779	snp	A/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124993564	GATCTTGGCAGTGCA[A/G]AGGTGAACCTGACAT	154214
rs186514524	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125028260	TATATGACAAAATCT[A/G]GGAGTATGTACTCCC	154214
rs186517768	snp	A/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125054343	TCTAAGGCTCCATGG[A/G]GAGCAGGAAGGGCAG	154214
rs186520325	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125073159	GATGCTTTGGGTTTT[C/T]GGCAGTTGTCTTCAA	154214
rs186529031	snp	A/G	0.0107246	0.0724382	intron-variant	RNF217	GRCh38.p7	6:125037037	CGATTCTTCAAGACT[A/G]ATTTTTTTAATGGAT	154214
rs186539539	snp	C/T	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:125017957	TCACATTTTCTGATG[C/T]GTTTAAAATATTTTG	154214
rs186544779	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125057852	TTAAATTATAAACTT[C/T]TAGCTAATTTCCCCA	154214
rs186545831	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125053541	TGATTTATTTAAAAT[A/G]ATGATGTGTATAGGG	154214
rs186551054	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124998522	ACTGTGTAGAAGGCC[A/G]GGTGCCGTGGCTCAA	154214
rs186558990	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125038256	TTTACACACGGAGCA[A/G]CAAAATATCTTTAAG	154214
rs186567463	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125020918	TTTTGGAGGGTTTTT[A/G]TATTTTTTCATTTGT	154214
rs186668537	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125062738	CCCACCACCATGCCC[A/G]GCTAATTTTTGTATT	154214
rs186669768	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125015875	TAGATTAATAAAATA[C/T]GGTATATTCATAGGA	154214
rs186672817	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035960	CATGTGCAGAATGTG[A/C]AGGATTGTTACATAG	154214
rs186677138	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125048529	CTTGTAATGTTTATT[C/T]TAATGTTATTCTGAG	154214
rs186678536	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125077505	CATAGTAGCCTCATA[C/T]ACAACCCCTTCCCAC	154214
rs186683985	snp	C/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125040406	GAAGAAGTTGAATCC[C/T]TGAATAGACCAATAA	154214
rs186687024	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124995214	ATTTTGTGAAATATT[A/G]TACATACAAAAGAAT	154214
rs186690847	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124978100	AGATAAACAATGTGT[C/T]CCTATAGAATAGTCC	154214
rs186714615	snp	G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125013188	CCAAAATGAGTCCCT[G/T]TTTTTTGGAGATTAT	154214
rs186723984	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975652	ATGTTGCCCAGGCTG[A/G]TCTTATACTCCTGGG	154214
rs186785612	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125054737	TATAGAGCAGTGCCT[C/T]TCAAACTTTAGGATG	154214
rs186797566	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125018244	TTCTTACTTAAGCCT[C/T]CCCCCTTTCATTTGA	154214
rs186817601	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979965	AAAGTGTTGGAAGTG[C/T]ATTGTCTTTAGTATA	154214
rs186963067	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037891	CCTTGTAAACTATCA[G/T]GACCAACACTTACAA	154214
rs186974622	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125020164	CAATTCGCAGACACC[C/T]GCTGGCTTGGGCTCA	154214
rs186980609	snp	A/C	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125072028	TAAATATAATTTAAA[A/C]CTATGTTTTAAGGCT	154214
rs186991881	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125003577	ATTTATATTTTAAAA[C/T]TGCTGAAAGAGTAGA	154214
rs187000067	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967021	GTTTCTGATCGCCAC[A/G]GTGAAGAGGTGAGCT	154214
rs187004004	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980186	GTCACTGGCCAAAAA[A/T]TTTGGAAACATCTTT	154214
rs187005959	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124999899	AAAAAGGTCCCAGAA[C/T]AATTATACCACCAAT	154214
rs187014112	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125037406	GTTGCTTCTTGTTAC[G/T]GTGTGTTTGGTATTG	154214
rs187016509	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964502	TAGTGTTTTTAATAA[C/T]ATTGGCTGGGACAAA	154214
rs187020750	snp	A/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124999203	TGATCTTTGGTATAT[A/T]TCATTTTAAATTTCC	154214
rs187046060	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964204	CAGTTTTCAATCTGT[C/G]ATGTTTCTGCCAGTG	154214
rs187078186	snp	G/T	0.0178098	0.0926698	intron-variant	RNF217	GRCh38.p7	6:125082293	CATATATTAGATGGG[G/T]TTTTTTTGCTAAATA	154214
rs187108349	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067122	CAGAAGAGGGAGATT[A/G]CAATTAAAACTGCAA	154214
rs187150524	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125076649	CCTTCCCTCTCTTGC[A/T]GATACAGATCCACAT	154214
rs187180615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039356	AAAAGACAAAGAAGG[A/G]CATTACATAGTGGTA	154214
rs187207269	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983160	AAGGGTCATAAATGC[C/T]CAGAAATTTTATGTA	154214
rs187372177	snp	C/T	0.178785	0.239642	intron-variant	RNF217	GRCh38.p7	6:125060382	ACACACACACACACA[C/T]ATATATTTGTACCCT	154214
rs187376089	snp	C/T			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963557	ATCTCTGTTAGTTTC[C/T]CACGTCTCAGTTGTT	154214
rs187380271	snp	A/G	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125022381	AACACATTAACAAAA[A/G]TAAGTAACAATTAAT	154214
rs187392716	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063751	AAGTTGTAAACAAGA[A/G]GTAATTACCACCATT	154214
rs187402604	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125078385	ACCTTTAATTTGGTC[A/G]TGGCAGTGTGTTTCC	154214
rs187405145	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125042070	ACTGTACTTCACTTA[A/G]TCATAATTAGTTGTT	154214
rs187411570	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005708	TACCATATTACATTC[A/G]AAATATGATTTCATG	154214
rs187414860	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125025943	AAGGAAAAGTTAAGA[A/G]TAAGGCCTTGAAGAG	154214
rs187421672	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124986252	AAGATTGCTATTTCT[A/G]TAAATGCCTTACCTT	154214
rs187514132	snp	A/C	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125000345	TCTTTTACTATAGTG[A/C]TAGTTGCTGTATATT	154214
rs187518801	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066358	AGAACCCGTCGCCCT[C/G]TGGACATGTCCCCAC	154214
rs187531473	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125046727	ATTTTGTAGCTTTGA[A/G]GGGACCATGGTTTAG	154214
rs187534685	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125010196	TCTAAAGGAATGAAG[A/G]TAGTGTTGTTAAGGT	154214
rs187540869	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029854	GTGAATTAGCTGAGA[G/T]GACGACAGCACTGTG	154214
rs187551494	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989983	TTTTGCAAAAGTTGT[C/T]TCCACTCCCATCTCT	154214
rs187556299	snp	A/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124973718	GTGGCCTGAGTCTTT[A/T]TGCTAGCATCCCATC	154214
rs187601238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050878	AGTGTAGTTTCTTAA[A/G]TGGTTGTTGTTGGCA	154214
rs187618830	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024853	ACGTAGATATCAGAA[A/G]CTTAGTATAGAGATC	154214
rs187627289	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979907	CAAGTGGTGGAGATG[G/T]CTCTGTCTCATGTCC	154214
rs187648916	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984505	AGTGCGTTGTGATCA[C/T]ACCTCCAGCCTGGAC	154214
rs187672875	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081554	ATTATCTGAGGGCCA[C/T]AGAGAGAATACGAGT	154214
rs187761544	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046277	AGTCTTGTGCAGTTT[A/G]CGCAGAAGTTTGGAT	154214
rs187782333	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088914	GCTCCTTTTTCTCTT[A/G]AATTTCCTAATTATC	154214
rs187864461	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124985027	TTAATGACATTAATG[A/G]CCAATAAATGTATAC	154214
rs187880849	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969804	ATAATAAGGGCAATG[G/T]AGAAGGAGAAATAAG	154214
rs187892102	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994365	TCTTTCAGTATGTAT[A/C]TCCCTAAAGTGAGGA	154214
rs187903996	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125004665	CTTTTTAAATGATCC[C/T]CTGTTTCACTTGTTG	154214
rs187905804	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047089	TGTTATTGTATAAGA[C/T]CAGGAAATTACTAGT	154214
rs187911248	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072453	ATTATTTGACCAACG[A/G]TATTTTAGTTGCCTG	154214
rs187933850	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124968956	ACCATGAGATACTCT[A/G]TAAATGTATTAAATG	154214
rs187942011	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125011857	AAAGAAACTCTTCTC[A/G]GTGAGATAATAACTG	154214
rs187952795	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124974249	ATTTTAAAACCTCCA[C/T]TACTTAAGAGAAAAA	154214
rs188008579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989882	GAAAAAAAAAACACC[A/G]ACAAAATAAAGACAA	154214
rs188019075	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125012244	TAAAAATGAAAGCAT[C/T]GCTAAGAGCTATCCT	154214
rs188029404	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992348	TATATTAAAACATGT[C/T]TTCTATTCCCAAATG	154214
rs188029522	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124972657	TGAGCCTTTACCTTT[A/G]GTGATATGAAGTTCT	154214
rs188042718	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124974530	CGTCAAGGTGTCAGG[A/G]TCAGCTTCCAATAAT	154214
rs188048273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069969	ATCCGAGCAGTGTAC[A/G]CTGTACCCATTACAT	154214
rs188082083	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124994627	ACTAGCATGATGTTA[C/G]GTAGATACAAAAGTT	154214
rs188101311	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075756	ATGATTATTCATGCA[A/G]CAAAGTACGCACAGA	154214
rs188119287	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125060151	ATTAATATTTGTTTT[A/C]TACTGTAAGGCTTTC	154214
rs188133493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039210	GCTGCATAGTATTCC[A/G]TGGTGCATATGTACC	154214
rs188206016	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125030269	ACAGCCAAACCATAT[A/C]ATTCTGCCCCTGGCC	154214
rs188224790	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055975	AAAGAGTAACATCCT[A/T]TTTTTCTTTTTTCAT	154214
rs188232981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991327	CTGTTCATCTTTCCC[A/G]TAATATTTACATGGC	154214
rs188265583	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069352	GGAGTTTTACACCTG[A/G]TAATTACCTCTAAAT	154214
rs188273846	snp	A/G	0.0337553	0.125452	intron-variant	RNF217	GRCh38.p7	6:125034772	ATGGCAACTGAATCT[A/G]TAAATTACCTTGGGC	154214
rs188297803	snp	C/T	0.00193694	0.0310599	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963065	TGGAGAGCGACCTGC[C/T]CGAGGCCCCCGCCTC	154214
rs188368677	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015758	CTCAAGAATTTTACT[G/T]CTAATTCACACACAT	154214
rs188388501	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977990	AGGGAGGAGAGCTGG[C/T]GTATTCTTATTCTGT	154214
rs188438936	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125079424	GGAGCCTTCTCCAAA[A/C]ATGAATACTCAATTA	154214
rs188445162	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125036918	TATTTATTATTTATT[A/T]TAAAGCAGGAAATAA	154214
rs188453386	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053884	TAGAAGAGTTTGTGC[A/G]TTGATCATAGTGCTT	154214
rs188457387	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017818	AGTAGTTATTCTGAT[A/G]CAAGCATAGCATAAT	154214
rs188461748	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125064747	ATGAGGACAAAATAA[C/G]TACGTGTGTATATAT	154214
rs188474345	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124979708	TACTTTATTTCAACT[A/C]TGATGGTAAATCTTC	154214
rs188478427	snp	C/T	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:124998417	CTGTCTGCTTATCTC[C/T]ATCTTCACTTTGTCC	154214
rs188571705	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125058202	TATAACTGTCTTAAT[A/G]CAGGTATGTGGAAAA	154214
rs188595175	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125039071	TGTTCTTGTTGTTCA[A/G]CTCCCACTTGTAAGT	154214
rs188602519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059574	TAGCCTGGTTCTACA[A/G]CTGGATTTGGAATGA	154214
rs188623312	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125001312	TTCTCCCTTGCCCAG[C/T]CCCCATTCTTAGAGG	154214
rs188623741	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982456	TTCCAGATACTTGGA[C/T]ATTTTCTATAGCAAA	154214
rs188640208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966420	CACATCAAAAGGGCA[C/T]AGTGAGTGCTTTCTT	154214
rs188670299	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125038689	GAAGACTATCAATGC[C/T]AATTTAATTGCTACA	154214
rs188716061	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041273	ACCTCTCAGTCATCT[A/G]TCATCTACTGCCTGT	154214
rs188720155	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125077937	GATGTTAGTGATAGA[C/T]TTCTATCAGGTAAAA	154214
rs188749327	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004962	TCTGGAGGATGGGAA[G/T]TCCAAGTGTATGGTG	154214
rs188767501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080550	GTTTCTCTCTTTCTC[A/G]TCTCTTATTGCATTT	154214
rs188768827	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976559	AGGTGTGAGCCACCA[C/T]GCTTGGCCTATTTAT	154214
rs188775550	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970284	ATCAGTTAGAAGACT[A/G]TGGAATAAATCAAAG	154214
rs188853976	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073680	GCCTATCTAGGAAAG[C/T]ACTCTCTAGTCCAGC	154214
rs188883696	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029131	CTTTTCAACCTAATT[A/G]CAAACTTTGCAGTAA	154214
rs188890261	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964566	TGTTTTTTGGCTAAC[A/T]CATGCTTGGGTCTAG	154214
rs188947137	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124992969	GTCTAAATTTTCCAA[C/T]GTAATAGAATATTTG	154214
rs188964800	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961957	TGTGGGGAGGTGTGC[C/G]CCAAAGGGGTGGGGT	154214
rs189003072	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063373	TTCATTATTTCTAGA[C/T]GACAGGAAGTTACTT	154214
rs189007222	snp	C/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125025736	AAAGTTGAAGGTGTT[C/G]TAGGGAGGGAGGAAG	154214
rs189010642	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125067632	AGTTATTTATTTTTT[A/G]TTGCAGTGGTGAGCC	154214
rs189027057	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002910	TCTGGGTCTACAGCA[C/T]AAGGCAATTATATCA	154214
rs189046841	snp	A/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125030784	CAAGCTGTCGGTGGA[A/T]GTACCATTCTGGGGT	154214
rs189054610	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966932	AAACATAGTTCTTCT[C/G]CAGTTATTGCCATGA	154214
rs189089671	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068029	ATTTAAAACATGTTC[A/G]TTATATTTTGCAGAT	154214
rs189103861	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF217, RNF217-AS1	GRCh38.p7	6:124964972	ATACACATTCCAGAA[A/G]TTCAAGGGAGGTAGT	154214
rs189107285	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083505	GTGAAACTAAATTAA[C/T]GAGAAGAATATTAAG	154214
rs189109496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030838	TGCAGCTCCACTAGA[C/T]GGTGCCCCAATAGGG	154214
rs189117854	snp	A/G/T	7.07889e-05	0.0059489	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048192	CCCAGCCAACCAATC[A/G/T]TGAGATTCATGGCCA	154214
rs189121960	snp	G/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125012485	TGTTTATACTACTTT[G/T]GATCTTCTGTTTAAA	154214
rs189167771	snp	G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124980516	TCATTTGCTTCCCCA[G/T]TTAATTCCTATTTAA	154214
rs189178451	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008852	AGCTGGTGGAGAGAT[A/T]TTCCTTATCAGCTCA	154214
rs189194509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986848	TCTTGAAATTTGTAA[C/T]ATAGATTTACTAATG	154214
rs189240868	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051374	TAGGCCAAGTGTGGT[A/G]TTCCTTATAAAATGG	154214
rs189248955	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089331	ATTCATCCAACCTGA[C/G]CCCAGGTCATTCATT	154214
rs189255925	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124987310	TGAGACCAGTATCAC[A/T]ACCTAATTTTGAAAC	154214
rs189256168	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036088	CCTTGCCCCCTACCC[A/C]CTGACAGGCCTCGGT	154214
rs189258144	snp	C/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007014	GTCTGTTTTTTATTT[C/G]TTCTGTTACAGTAAT	154214
rs189273553	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:124971491	AGACGGAGTCTCACT[C/T]TGTCACCAGGCTGGA	154214
rs189273742	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016517	ATGGAATCTGTGCAG[A/C]AAAGTATTAACAGGG	154214
rs189285921	snp	A/T	8.85951e-05	0.00665505	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082916	ACAGAGAAAACGATC[A/T]CGGACAGGTATGCAC	154214
rs189309177	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090882	ACTATTAACTTTGAT[A/G]ATCACAAAACTATGT	154214
rs189311867	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047425	TGAGAGTGAAATATG[C/T]AAAAATTGACAAATA	154214
rs189316135	snp	A/G	0.0123036	0.0774623	intron-variant	RNF217	GRCh38.p7	6:125021959	TGATCTCAGCTCACT[A/G]CAACTTCTGCCTCCC	154214
rs189330925	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983062	GGAAAAGCTTTCTAT[A/G]TATTTCTTCTTCAAC	154214
rs189362381	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125026284	GTGACTAACATTGAA[C/T]TAAAGCTTTAGTACT	154214
rs189457613	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006434	ATTTTACTTGTACTC[A/C]TTTTTTCTATTATGT	154214
rs189475053	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124970779	GACATCAGAAAGAAG[A/C]AGCAAAGAGTCTAAA	154214
rs189487700	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125074546	ACATAATTTGGAGTT[A/C]GGAACTTCAAAAACT	154214
rs189624234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071252	TTTGGTAGAAACCAT[A/G]TTTCAAATTTTGAAT	154214
rs189656091	snp	C/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125042945	CAATAACAAGTGCCT[C/G]TCGAGGTGGCCCAAG	154214
rs189671182	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125048552	ATTCTGAGTCATTGA[C/T]TCACAGTATCTTCAT	154214
rs189673098	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084764	TAGCATATTTCTAAA[G/T]CATAATATAATACAA	154214
rs189680951	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014029	TTTATTTGTCTGCCT[A/G]TTGTTCTCTGAATGG	154214
rs189685915	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125031743	CTTTCCCACATTTTC[A/C]TATCTTCTTCTGAGC	154214
rs189699414	snp	A/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:124994165	GGATGTGTGTGTATC[A/T]TTTTGTTTTATAAAT	154214
rs189710539	snp	A/G/T	0.00199529	0.0315338	intron-variant	RNF217	GRCh38.p7	6:125077791	ATCTTCCACATTTCC[A/G/T]TTTTCCTTCCTACTT	154214
rs189754984	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125031217	TTTTTCCTCCAGCGC[C/T]TCCAGGCCTGTGATG	154214
rs189816979	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125072626	AAATTACAGTGAAAA[A/T]TATATGTGAAATATG	154214
rs189839438	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071072	CACATTCCAGTTCTT[A/T]TTTTTAGATACTTTG	154214
rs189847394	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125036319	ATTTTCTTTATCCAG[C/T]CTATCATTGATGGGC	154214
rs189849030	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056007	TTTTTACTTAAACCA[A/G]GTAGTTTCTCAATTT	154214
rs189857940	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997729	TTTAATCTGCTCGCT[C/G]TCTCTACAGCCCTGA	154214
rs189920557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068454	CATCTATTGAGTACT[A/G]TCTTCATACTTTCTA	154214
rs189993100	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125021160	ATTTATAATAGCATT[A/C]AGTTGGAGACAGCCT	154214
rs190011780	snp	A/C	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124984123	AGCAAACATTCACAC[A/C]ACAGCAATAAGTTAA	154214
rs190015645	snp	C/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981676	GGACTTGTGAAGATA[C/G/T]GCTATCATATATTGC	154214
rs190024273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124968565	AGCAGGACTTTTTCC[A/G]AGGCATGCTGCATGG	154214
rs190080100	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090056	AAGTGTCATATGGCA[A/G]CTCCTCAATAGCTTA	154214
rs190086554	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052832	TTAGTTTCTTTAGGA[A/C]ATACCCGAATCTGAC	154214
rs190097414	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017004	TCCATGGGATACTAC[A/G]TAGCCATGAAAAGGA	154214
rs190119329	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979350	GAGAAAGGAGTTAGG[C/T]GTGGGCAGCTCTCTA	154214
rs190156856	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077413	CAAATGCCCTCAGTG[A/C]ATACAAACCCAAGTT	154214
rs190167479	snp	C/T	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125062420	TCATGATCAAGATAC[C/T]TACTTACAAGTATGA	154214
rs190181721	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125040070	TTCAAAAGCTAACAG[A/G]AGACAAAAAATAACT	154214
rs190196398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004144	ATCTAAAAGGAAATA[C/T]TAGACAAATGTTAAA	154214
rs190196638	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024219	TTTGTTGATGGTTGA[A/G]GGAGAGAGGAAGCAG	154214
rs190246878	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975198	ATTCATGAAACTCAT[A/G]AGCTCTGAGTTGTAT	154214
rs190263435	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000943	TCAAAAGTATGGAAG[C/T]ATGATGTATGAGAAA	154214
rs190319583	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125065399	TTTACCAATATGAAT[A/G]TCCGATGCATTTAAA	154214
rs190333884	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044853	ATGCTGCCTGACCCC[A/G]CAGTTCTTGCAGTTG	154214
rs190343829	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124979981	ATTGTCTTTAGTATA[A/G]CAGAACGTCCTTGCA	154214
rs190344236	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007608	TGTTCTGTTTTCTTC[A/G]GTGCTTGGGGTGCAG	154214
rs190345473	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124978380	TGGCTCTGCGCTCAG[C/G]CCATGGATCAACCAG	154214
rs190348256	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964249	GGATGCCCTTTGATC[C/T]TGTGTCCAATTGTCC	154214
rs190350106	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125027532	ATTGTGTATATGTAC[A/C]ACATTTTCTTTACCA	154214
rs190363937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987993	CAGGGATCAATCCCC[A/G]GACTGTTAGGAACCA	154214
rs190466587	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079828	TATTTAAATAAAATA[C/T]GATATATGGATATGA	154214
rs190549273	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064874	GGGTACTAGAAAATG[G/T]AGTGTACCTTAAAAC	154214
rs190557715	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125026879	AGTTATAGAGTAGTA[G/T]TATTTTCACATGCAA	154214
rs190592430	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124997157	AATTTCTGTTTTGAC[A/C]AGGCATAGAAAAGAG	154214
rs190596869	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040686	ATTGAAGCGAAAATC[A/T]TCAATAAAATACTGG	154214
rs190599183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004786	AAAGTCTCACTACTT[C/T]ATATTAATAATTACA	154214
rs190601609	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961569	TTAAATTAGTTATCA[A/G]CTCTTCTAAGGATTC	154214
rs190605313	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125068658	CAGTTGGTTAATGTC[C/T]GTATACATGTATAAG	154214
rs190690645	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124983720	AGGAAGAGGCTTGGA[A/G]TTAGATGATTTGGGT	154214
rs190694759	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967903	CCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGATTA	154214
rs190776681	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125068709	TGTCAGATTTTATCA[A/G]TGAACAAAGTAATTA	154214
rs190778796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032948	TTTGGGGAACCTTTA[A/G]GTACTATGATAACTC	154214
rs190783207	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049298	GATTTTATGATATAT[A/G]TGTGTGGTTATTTGC	154214
rs190795612	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125015280	ATATCTTCATTAGAT[G/T]TATTGATTTTAAAAA	154214
rs190840892	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025194	TAACCAGAAGGTGAT[G/T]GATAATTTTGTAGAG	154214
rs190854883	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125048894	TGTTCTGAACATCGT[C/G]AAACTCATACTATAT	154214
rs190924268	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125065827	TTTAGCTGTTGGCTC[A/C]GTCGGTAGGCAAATC	154214
rs190937191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028273	CTGGGAGTATGTACT[C/T]CCAACAATGCACAGG	154214
rs190938728	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124972795	CCCCCTATATCTAGA[A/T]TAAGCATCCTTCCTA	154214
rs190960719	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989154	GTGTGATGGAATTTT[G/T]TTTTAATTTACTATT	154214
rs191014634	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086447	TTGGTGATACTTTTC[A/G]CATTTTTAGTAACAC	154214
rs191022728	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125062931	TTTTTTATCTTAACA[A/G]TGAGTTTTCTATTTA	154214
rs191086182	snp	A/G/T	0.00319098	0.0398384	downstream-variant-500B	RNF217	GRCh38.p7	6:125092825	GTGTTGCTGTGGCAC[A/G/T]TTTTGGGGAAAGAGC	154214
rs191094977	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995335	CCATCCAAAACACAC[A/T]GTGCACTCTGATTCA	154214
rs191098024	snp	A/G	0.0422008	0.138995	intron-variant	RNF217	GRCh38.p7	6:125013551	CAGAATATGTCTGGG[A/G]AAAAAAAAAAAGTAG	154214
rs191104815	snp	A/C	0.0279526	0.114869	intron-variant	RNF217	GRCh38.p7	6:124978314	GCTCCACCTGCTTAG[A/C]CCGGCAGGCTGCATT	154214
rs191110356	snp	C/G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125054430	TGGTAGTGTGAGAGC[C/G/T]CTTCTGTCATCTCAC	154214
rs191110910	snp	G/T	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960802	CACACATAAGTAGGT[G/T]TCTTGTCTCTGTCTT	154214
rs191112595	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009382	CTCACAGACATAGAG[C/T]CTGGAAGAGTAGATT	154214
rs191114596	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029695	CATTTTTTAAAGTGT[C/G]AAACGTTGATTACCT	154214
rs191116571	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975715	GTGCTGGGGTTACAA[C/G]TGTGAGCCACTGCAA	154214
rs191121662	snp	A/C	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124989891	AACACCAACAAAATA[A/C]AGACAACAAAACCCC	154214
rs191123721	snp	A/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125037181	ATCTATCCTTGTGCC[A/T]CTGTCACACTAATGT	154214
rs191165248	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045549	CTTTCCTTTATGGAG[C/T]TGAAGGTGAGCATAT	154214
rs191200763	snp	G/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125008783	TTTCCTTCTCTTTGT[G/T]TCAAGCTTAATTAGG	154214
rs191211123	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972493	GCTTCTTGCTAATAG[A/T]TTAGAATTTAAACTT	154214
rs191237535	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070070	CTTTGCATCCCCATA[C/G]CTTAGCTCCCACTTA	154214
rs191257926	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036015	CTGCACCCATCAACC[C/T]GTCATCTAGGCTTTA	154214
rs191266160	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125050893	ATGGTTGTTGTTGGC[A/G]TAGATTTATGAGACA	154214
rs191269991	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015923	TTTCAGCAAAAAAAA[A/T]TAAATTTTTGTTCAC	154214
rs191340494	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124993804	TAAAGAAGGGGCTGC[A/G]TAAAGAGTGTGTCAG	154214
rs191403332	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037445	TACTTGATGTACTTA[A/G]ATGTTTTCTTTGTAC	154214
rs191407899	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124999583	CCTAAAGTATAACTA[C/G]AGTCAAGCCAGGTGA	154214
rs191410683	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125038051	CCTGAGTCATTAAAT[A/T]ACTTTTGAGTTCTCC	154214
rs191428350	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125020441	TGGTATTCACAAGTC[C/T]GCCTAGTTTTTACTT	154214
rs191438053	snp	A/G	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:124980215	TTTGCGAAGATGTCC[A/G]TAATTATTTCACTGA	154214
rs191438265	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999901	AAAGGTCCCAGAACA[A/G]TTATACCACCAATAG	154214
rs191447909	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124972106	TTCCTCCCCTTGTTT[A/G]CCACATGCTCAAAGC	154214
rs191452453	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964540	GGGCTCCGTACCATG[A/T]GATTCCTCTATGTTT	154214
rs191563665	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072261	TCATATATAATCAAG[A/G]TATATTCATAATAAT	154214
rs191634723	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125055434	ATGCCTTAGGAGAAT[C/G]ATGCATTGCTATAAT	154214
rs191646704	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125018907	ATCCATATAAAGGGT[C/G]GTAAGTCTCCCCGGA	154214
rs191747655	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125061411	CTGTTTGCTTGTAAA[C/T]TGAATATAAATTCAT	154214
rs191751667	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125022389	AACAAAAATAAGTAA[C/T]AATTAATGTTCTTTC	154214
rs191755036	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994447	AATATCATTATATAT[C/G]TAGTCAGTGTTCAAA	154214
rs191791330	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125078605	CCTTGATAACTAACA[C/T]GCTCCTATGATAGTG	154214
rs191807416	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064298	GAGCAGGGGTTATCA[A/T]TGGCACTGTTTTTAT	154214
rs191822503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042813	GAAATTGCTGCTTCC[A/G]TTGCTATCATTTACA	154214
rs191829280	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005931	TTCAGATAAAAATCA[G/T]TTATACTGTGCCAGC	154214
rs191833130	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026070	ATCTGCTTGTCCACA[A/G]CACTGAGGGAGATGA	154214
rs191843854	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:124986270	AATGCCTTACCTTCT[C/T]TTGTGACCTTGTTTT	154214
rs191888097	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018104	TGTTTAAGAAAAGTT[A/G]TATGTTTTTTATAGA	154214
rs191903061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979944	TTACTGGATCTTTGC[C/T]TTTAAAAAGTGTTGG	154214
rs191957143	snp	A/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125010795	TTAGTAGTCTCCCTG[A/T]TGCTGCTGTGCCTGG	154214
rs191959791	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981884	AAAAAAAAATTTGGC[C/T]GGGCGTGGTTATGGG	154214
rs191961920	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965553	ACTCCAGCCTGGGCA[A/G]CAGAGTGAGACTCCT	154214
rs192017206	snp	C/T	0	0	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081520	TCGGTAAGAAACACT[C/T]CATGCATCTGAGATT	154214
rs192020015	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046471	ACACACCAGTGCCCC[A/T]GGCCCACCCCAGAAC	154214
rs192036640	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039854	TGAATGACTCCTGGG[C/T]AAATAACGAAATTAA	154214
rs192058606	snp	A/G/T			intron-variant	RNF217	GRCh38.p7	6:124976591	TATTTTTTTAGATAG[A/G/T]TTCTTCATAGTGATT	154214
rs192072642	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003626	ATATAAGGTGATGGA[C/T]TTGTTAATTAGCTTG	154214
rs192118710	snp	A/C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081753	AAAGCATTATTAACC[A/C/T]TTTTATAACACAAAG	154214
rs192139101	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066496	GACTTGCCTTGTCCC[G/T]CTGTCTGGAATGTTC	154214
rs192147144	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125030045	GGAGGTGAAAGGCAT[C/T]TCTTACATGGCAGCA	154214
rs192153213	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125000961	GATGTATGAGAAATG[A/T]CTTTCAATTACATAT	154214
rs192154384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046746	ACCATGGTTTAGCAG[A/G]TAGTTTCCTCTGCTG	154214
rs192166303	snp	A/T	0.00835141	0.0640778	intron-variant	RNF217	GRCh38.p7	6:124969049	AAATAAGCTTTTTTT[A/T]AAAAAAGTTACTAGA	154214
rs192192036	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999047	AGCTTGCAGTTGATT[C/T]ATAGCAGTATTTGAC	154214
rs192204622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036174	GAGTGAGAACATGCA[A/G]TGTTTGGTTTACTGT	154214
rs192211147	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963611	TGGTTTACTTAACTG[A/G]AATTTAACTTTGCTG	154214
rs192299177	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985973	TCCCAAAATTCATGT[A/G]TTGAAACTCAGCCAT	154214
rs192300764	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005229	GTTAGGTTTATAACT[A/G]CTATGGAAAGGACTG	154214
rs192315930	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124969869	AAATCTATAGTTTTG[G/T]GGGGGTTGTCATGGA	154214
rs192373361	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125070598	TCCCTGATAATTAGT[A/G]ATGCTGAGCATTTTT	154214
rs192388388	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125051781	TCTTGTGAGCTGTTA[A/T]CCTGATTCTGTTGTG	154214
rs192388681	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089538	TGTAACTGATATTAA[C/T]CCTATTCTAGAGAAA	154214
rs192433025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067135	TTACAATTAAAACTG[C/T]AAAGGCACAGAGCCA	154214
rs192435122	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125030319	CACATTTCAAAAACA[A/G]TCATGCCTTCCCAAC	154214
rs192449851	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124991576	GGCTGTAGGCCATGA[A/G]GATAAGAATTTTGTT	154214
rs192530576	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047539	TCAATTTGTTGTAGG[C/T]AAGAAGAGAAGCAGG	154214
rs192548244	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073232	GATTCAGAGGTCCAG[C/T]AGGGCTGTTGGCCTG	154214
rs192555630	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984751	TTTTCTGATGTCTGT[A/G]TAACCTTAGTATGGA	154214
rs192701013	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088994	AAATTCTGTCTCGCC[C/T]GTAACTCCTTTCACT	154214
rs192725717	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088377	GATTTTGAAAATAGA[A/G]CAAATACACATTTCA	154214
rs192733523	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125050586	TCAATCGGTTGTTGC[A/G]AACTGGTGTACTTTA	154214
rs192746468	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015774	CTAATTCACACACAT[A/G]TGTAACATGTAAAGG	154214
rs192749345	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977991	GGGAGGAGAGCTGGC[A/G]TATTCTTATTCTGTT	154214
rs192766410	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047200	GAGACTATACTAATT[C/T]TTAAAATTGCAGTAA	154214
rs192781582	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125011899	TTTTGGTGCTGAGTT[A/C]TTGACTCTTTCCTCT	154214
rs192789848	snp	A/T	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124974311	GAATTTTAATTTTTT[A/T]AAAAAATTTTGTCTT	154214
rs192813911	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124973901	CAGTCAGTTCACTTT[C/T]GGGGTTTCTCATTTG	154214
rs192853915	snp	A/T	0.000248392	0.0111415	intron-variant, missense	RNF217	GRCh38.p7	6:125082545	TGTTAAGTGATATGC[A/T]ATACTGCCTGAAACA	154214
rs192885714	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125038739	CAGGATTCACGGCTT[A/G]ATTCACTTTATACTA	154214
rs192888751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073749	GGGACTGCCTGGCAG[C/T]CCAGGAACTTGCAGT	154214
rs192931191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069390	TTTTACACCTAGTCC[C/T]TGATATTTTCTATTG	154214
rs192950843	snp	A/C	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:124994725	GTGCTAGTAAGTGCT[A/C]CTTTAGGCAGTTGTA	154214
rs192951759	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124970479	AAAACTGGGGTTGCC[A/G]TTTAATAAGATGAGG	154214
rs192961422	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997431	ATATGCGAAAGTGAC[C/T]GTAAATCACATAGAC	154214
rs192964574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063578	ATATATTGTCTCATC[C/T]AAACTTCAGATGTGA	154214
rs192969767	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025775	GGAGGGAGGGAGGGA[A/G]GGAAGGAAGGAAGGA	154214
rs193022398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990502	GTTTTATTTATAGTT[C/T]TCACCATTTCAGTTG	154214
rs193097332	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083348	ATAGCTGAAGTCCTA[C/G/T]CTGTACCAACAAGCA	154214
rs193106624	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125058445	AGTTCTAGTCTGCCA[A/C]GTGTACTATAATTAC	154214
rs193116814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021012	AATAAACATGGCTTT[C/T]AGAAAGCAGTTTGGC	154214
rs193117824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124981324	GAAAGTTTATTTTGC[A/G]AAGTTAAGGATGCAC	154214
rs193118511	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021188	CCTCCATGTGGAGTT[G/T]AACTGTGGTTCCTCT	154214
rs193182977	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041751	CTGTCTTGTTTATTT[G/T]CTTGTTTACTATTCA	154214
rs193183523	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125077947	ATAGATTTCTATCAG[C/G]TAAAAGATAGAACAT	154214
rs193184314	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016743	GAACAATGACAACAC[A/G/T]TGGACACAGGGAGGG	154214
rs193188271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978813	AATAAGGTACGTGGA[C/T]ACATGGACACCAGAG	154214
rs193255750	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067797	CTACCTTTGTTGGAA[A/T]AAAGTTGAAACCATT	154214
rs193267580	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038342	TGTTAACTTGATACT[A/T]AAAAATTGACATTTT	154214
rs193269407	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125000599	GATCCTCACATTAAT[C/T]AGGTATTCTAGGAAA	154214
rs193275935	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964594	TAGACTGAAAGTGTG[C/T]ACAGTCCCTAACTAA	154214
rs199503551	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125044059	TTACTATGAATTTAG[G/T]TTTTTTTTTTAATTG	154214
rs199552347	snp	A/G/T	3.3349e-05	0.00408333	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045398	TTACAACCTTCAAGA[A/G/T]AAAAGGACATATTCC	154214
rs199633519	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976980	TAATTTTTTCCTGAT[A/G]CTTTGCTCGTTTTTT	154214
rs199754035	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030575	GTCCAAAATCCAGTA[A/G]GGCAGTCCAATTTTA	154214
rs199816894	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040285	ATCCCACAGCAATAG[A/G]AACTACCATCAGAGA	154214
rs199898996	in-del	-/G	0.00993419	0.0697739	intron-variant	RNF217	GRCh38.p7	6:125013556	ATGTCTGGGAAAAAA[-/G]AAAAAAGTAGTCTGA	154214
rs199936265	in-del	-/TAAGGGA	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF217-AS1, RNF217	GRCh38.p7	6:124960528	CAGTAAGCTGGAACC[-/TAAGGGA]TAAGGGATAAGGAAT	154214
rs199943363	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124977449	AGATTATAAAATAAT[A/C]AAGCCAGTTCTAAAA	154214
rs199958328	snp	A/C	0.00199792	0.0315431	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045244	GAAATCAAATGCCCC[A/C]TCACAGAGTGTTTTG	154214
rs199981900	in-del	-/A	0.0228947	0.104514	intron-variant	RNF217	GRCh38.p7	6:125040131	CATGAAAAAACCTTC[-/A]AAAAAAATCAATGAA	154214
rs199994295	in-del	-/T	0.157311	0.232183	intron-variant	RNF217	GRCh38.p7	6:125069858	TGAAATCTCAGGGGA[-/T]TTTTTTTTATTTCAA	154214
rs199995373	snp	C/T	3.29832e-05	0.00406085	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076782	CCACACATCAAACCT[C/T]AGTATATTTGGATGC	154214
rs200014198	in-del	-/T	0.0162398	0.0886349	intron-variant	RNF217	GRCh38.p7	6:124989020	TCTTAAACCAGTTTA[-/T]TTTTTTATAAGCATA	154214
rs200089921	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124992405	GGAGAAAATAAGAAA[A/C]TAAGAGGCTATAGAA	154214
rs200091142	snp	A/G	7.10808e-05	0.00596115	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082918	AGAGAAAACGATCAC[A/G]GACAGGTATGCACTG	154214
rs200103611	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124989057	CTACAATATAATTTA[G/T]TTTGCTTGTCTAACA	154214
rs200178529	in-del	-/GGAG	0.101658	0.201233	intron-variant	RNF217	GRCh38.p7	6:125025756	GAGGGAGGAAGGGAA[-/GGAG]GGAGGGAGGGAGGGA	154214
rs200196122	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984554	CTCAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAAA	154214
rs200247125	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125035885	CCTCATCTGTTGAAG[-/T]TTTTTTTTTTCAATT	154214
rs200280514	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125017497	TATAAATTAGCTATA[C/T]AAAACAAGTGTATGA	154214
rs200438375	in-del	-/A	0.338296	0.233889	intron-variant	RNF217	GRCh38.p7	6:125013550	GGGAAAAAAAAAAAA[-/A]GTAGTCTGAAAGCTT	154214
rs200458642	in-del	-/TT	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:124978201	ATGTATATGAATAAA[-/TT]TTGTGTTACAGGATT	154214
rs200508993	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989065	TAATTTAATTTGCTT[A/G]TCTAACAAATGTGCC	154214
rs200530162	snp	A/G	0.000231541	0.0107572	intron-variant	RNF217	GRCh38.p7	6:125045176	AAAATAACCAGTGAC[A/G]TTTTTTTCCTTCCAT	154214
rs200547061	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125055192	TTTAATCCAAAGCAA[A/G]TAAAGAGTGATTCTG	154214
rs200551877	in-del	-/G	0.0379877	0.132479	intron-variant	RNF217	GRCh38.p7	6:125003373	TGGTTTTTGGTATGT[-/G]GACCTTGGAAAAGTT	154214
rs200556806	in-del	-/CAAGTTTAGGTT	0.0659589	0.169201	intron-variant	RNF217	GRCh38.p7	6:124997018	TTTGTAGCACTCCTG[-/CAAGTTTAGGTT]CTACAAACACGGACG	154214
rs200597285	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125033198	ACAGATTCTGTGTTC[-/T]TTTTTTTTTTTTATA	154214
rs200600117	in-del	-/C	0.0501905	0.150254	intron-variant	RNF217	GRCh38.p7	6:124975954	TATGTTATCATTTTT[-/C]TTCCTCAAGATATTT	154214
rs200609152	in-del	-/A	0.0486741	0.148216	intron-variant	RNF217	GRCh38.p7	6:125059144	ATAAATATAGTAAGG[-/A]AAAGTATTGTATGAA	154214
rs200620896	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125034737	ATTCTGTGAAGAAAG[G/T]CATTGGTAGCTTGAT	154214
rs200714912	in-del	-/TCC			intron-variant	RNF217	GRCh38.p7	6:124975956	TGTTATCATTTTTCT[-/TCC]TCAAGATATTTTTTA	154214
rs200735539	in-del	-/A	0.0134861	0.0810011	intron-variant	RNF217	GRCh38.p7	6:125016633	ATACTGTGCAGCCAT[-/A]AAAAAAAAGGATGAA	154214
rs200739951	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124989066	AATTTAATTTGCTTG[C/T]CTAACAAATGTGCCA	154214
rs200777753	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125048605	TTTATTATGGCTTTT[G/T]CTGTCAATTCAACTG	154214
rs200806930	in-del	-/GA			intron-variant	RNF217	GRCh38.p7	6:125038243	TTGTATTAGCATTTT[-/GA]ACACACGGAGCAGCA	154214
rs200828294	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033369	CCCACAACAGTCCCC[A/G]GAGTGTGATGTTCCC	154214
rs200841510	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125062585	GTTTGTTTGTTTTTG[-/T]TTTTTTTTGAGATGG	154214
rs200922013	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125013389	TGTGTGTGTGTGTGT[C/G]CTGTTTTTGAGAGCA	154214
rs200924116	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125072852	TAGCATAATAAAGAA[-/AC]ACACATGGATTCAAA	154214
rs200965420	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125005395	AGACAAATATGGCTT[A/C]CATAACATAAGGGTA	154214
rs200985721	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088014	ATAAGTTACAAAATT[C/T]TTTTTTTTTTTTTTT	154214
rs200992365	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125036412	GTGTCTTTATAGTAG[A/C]ATGATTTATAATCCT	154214
rs201025136	snp	C/G	0.000413001	0.0143642	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057990	TTTAAGTGCCACTCT[C/G]CTTGGCATGAAGGTG	154214
rs201052779	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125050260	CATGTTAGAGAACAC[A/G]TTAGAGGTAATTCTT	154214
rs201056103	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124989060	CAATATAATTTAATT[A/T]GCTTGTCTAACAAAT	154214
rs201070145	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016745	ACAATGACAACACGT[G/T]GACACAGGGAGGGGA	154214
rs201083719	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125059316	CACCCATTTTGTTTT[A/G]GAGCTATTTCAGATC	154214
rs201121254	in-del	-/C	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:124989877	GCTTGAAAAAAAAAA[-/C]CACCAACAAAATAAA	154214
rs201121902	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001220	GGAATGCTGAATTTA[A/G]TATTTATGTGAAATT	154214
rs201161973	in-del	-/TC			intron-variant	RNF217	GRCh38.p7	6:125014195	AAGTGATCCTGGAAT[-/TC]AGATTGAAAGCTCTT	154214
rs201163820	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125052292	TGCGTTTTGTGTGTG[-/TA]TGTGTGTGTGTGTGT	154214
rs201177267	snp	A/G	0.000246796	0.0111057	intron-variant	RNF217	GRCh38.p7	6:125057903	TTAGACACTTTCAGT[A/G]TATCCACTAGTAATT	154214
rs201237639	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125060354	GAAAGTATATATGTG[-/TA]TACACACACACACAC	154214
rs201239570	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125032466	ATGCCAAATATATAA[-/AT]ATATATATATATATT	154214
rs201289522	in-del	-/A	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125018314	GACTAATGGAAATCC[-/A]GGGGGCACTGGTATT	154214
rs201315163	snp	A/T	0.000461437	0.0151824	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009246	ATTAGTTCTCTTCTC[A/T]TCCACACCCATAAAC	154214
rs201332552	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124996956	TTAATATGGTTTAGT[A/G]TTGACAGTGGAGATG	154214
rs201376226	snp	A/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961544	GTAGGCGAAGAAAAA[A/G]AGAGAAATTTTAAAT	154214
rs201403427	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125034856	CTTCCATTTGTTTGT[A/G]TCCTCTTTTATTTCA	154214
rs201462320	in-del	-/CT	0.0240643	0.107019	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085862	CTTACTGTGCTGTGA[-/CT]CTTTGTCATTTTATT	154214
rs201569512	in-del	-/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960674	GGGAATATACTTTTT[-/G]GCATCCATTATTGTT	154214
rs201610631	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091357	TGACTTTATTTCTTA[C/T]CTAAAGAGCCATATA	154214
rs201640818	snp	C/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967735	TATCCTATTATTAAA[C/T]TATGAGTCATCCAAA	154214
rs201688463	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125046603	TTCATCCTTGTCATT[A/C]CAGCAAAATGGCAGG	154214
rs201725057	in-del	-/AG	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124979053	CCAATAGAGAGAGAG[-/AG]TGTAAGATGGTGATA	154214
rs201731528	in-del	-/G	0.0138799	0.0821421	intron-variant	RNF217	GRCh38.p7	6:124965638	TGAGTCATAGATACC[-/G]GGGCATGCTTTCACC	154214
rs201736140	in-del	-/A	0.00953873	0.0683987	intron-variant	RNF217	GRCh38.p7	6:125067921	GAGAGGAGAAACTGG[-/A]AAAAAGATGTCACTG	154214
rs201765315	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033401	TTCCTGTATCCATGT[A/G]TTCTCATTGTTCAGT	154214
rs201780011	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004073	GTTACAGTTTTTTTC[A/G]TTAAAATTCATCCAT	154214
rs201795062	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124989068	TTTAATTTGCTTGTC[A/T]AACAAATGTGCCATT	154214
rs201800968	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125079454	AAAAAAAAAAAAAAA[C/T]ACAAGCCTGGAGCCA	154214
rs201802744	in-del	-/T	0.120326	0.21374	intron-variant	RNF217	GRCh38.p7	6:125002446	CCCCCTGCACGCCCC[-/T]ATCCCCATCTTCCCT	154214
rs201866852	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125013547	GGCCAGAATATGTCT[-/G]GGGAAAAAAAAAAAA	154214
rs201939360	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124978678	CTCAGTGGGCAGAAG[G/T]GAGGGTTACAGATCA	154214
rs201991785	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965114	TTTAGTAATGGTAGT[A/C]GGGAGACAGAGGGAC	154214
rs202166775	snp	C/T	0.00199806	0.0315443	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009257	TCTCATCCACACCCA[C/T]AAACCAGTTCAAGAA	154214
rs202208843	in-del	-/T	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125022851	CACCTATGTCCCTGC[-/T]TTGACCTTGAGTTTT	154214
rs202210592	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124989061	AATATAATTTAATTT[C/G]CTTGTCTAACAAATG	154214
rs202245999	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970584	GAGTAGGCAGTTGGC[A/G]TCTGGCATTCAGAAG	154214
rs267600789	snp	C/T			missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057991	TTAAGTGCCACTCTC[C/T]TTGGCATGAAGGTGT	154214
rs267600790	snp	C/T	0.000134571	0.00820168	RNF217	6	allele_origin=T(somatic)/C(germline)	6:125081506	CATAGCGGTTGTAAT[C/T]GGTAAGAAACACTTC	154214
rs367545061	in-del	-/AGAGT			intron-variant	RNF217	GRCh38.p7	6:124980701	GTTTTTGGTTAGAGT[-/AGAGT]GATAAAGTAACAACT	154214
rs367562544	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086971	ATGAACCACTGTAAT[A/C]ATTTCCAGTCCCTGA	154214
rs367587258	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965069	GTTTTCTTTTTCTTT[A/G]TTAAACCTCATAAGT	154214
rs367624050	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125042966	GTGGCCCAAGTAAGC[A/C]CCTTTTCTGTGGACT	154214
rs367707620	in-del	-/GC			intron-variant	RNF217	GRCh38.p7	6:125013389	TGTGTGTGTGTGTGT[-/GC]TGTTTTTGAGAGCAT	154214
rs367793065	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084919	TAACCTGTCATAAGA[G/T]TAAGGTTTCGTAAAT	154214
rs367852675	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125021824	GGAAGATCAGACATT[G/T]TGCTCTTCAATAAGT	154214
rs367902852	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125078401	TGGCAGTGTGTTTCC[G/T]TCCATTCTTTATTTT	154214
rs367904403	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125029638	GACCAAACTCTGTAG[A/G]GGGGAGAAGTGTAAA	154214
rs367910475	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125034120	AGATGAGTAGGTTGC[A/G]AAAATTTTCTCCCAT	154214
rs367986091	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994293	TATCTATTCCCACTC[A/G]CTTCCCCTTCCCTTC	154214
rs367992124	snp	A/G	0.000165552	0.00909662	intron-variant, missense	RNF217	GRCh38.p7	6:125082539	CTGTGTTGTTAAGTG[A/G]TATGCTATACTGCCT	154214
rs368094518	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050585	ATCAATCGGTTGTTG[C/T]GAACTGGTGTACTTT	154214
rs368109911	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086339	AAATAAAATTTGAGG[A/T]GATGTGTGTCAGATA	154214
rs368118479	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993321	CAATATAAATAGAGT[A/G]CCTAGAACAATAACT	154214
rs368150570	snp	C/G	0.000629405	0.0177287	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962934	GGAGGCGCCCCCCGG[C/G]GAAGAGCTGGAGCCC	154214
rs368166513	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125054856	TCAGGTGATGCTGAT[G/T]TTTCTGGCCCTGCAA	154214
rs368174059	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052775	TTCAGTTTTTAAAAC[A/G]TTTTTATAACTACAA	154214
rs368177349	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041692	GTCATTTCCTTAGAG[A/G]TTGCTTCCATGATGT	154214
rs368185339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013064	TTGAAACATACTTGA[A/G]ATAATTGACATTTAG	154214
rs368229344	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981814	ACTAGGTCAAGAGAT[A/G]GAGACCATCCTGGCG	154214
rs368318530	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125063670	CTTTAAGGTTTTGCA[C/T]AATAATTATAACATA	154214
rs368400078	snp	C/T	0.000399281	0.0141238	intron-variant, splice-donor-variant	RNF217	GRCh38.p7	6:124996657	GAAGCATATACAGTG[C/T]GAGCATACTCTTTAA	154214
rs368426155	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988731	TTTAAACTTCTCTAA[C/T]TAAAGTTCTTTAATC	154214
rs368469313	in-del	-/TG			intron-variant	RNF217	GRCh38.p7	6:125052285	CCTTGTCATGCGTTT[-/TG]TGTGTGTGTGTGTGT	154214
rs368494115	snp	A/T	1.65282e-05	0.00287469	synonymous-codon, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045282	GGAAGAAACAACTGT[A/T]GTCTATAACTTAACG	154214
rs368685374	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049404	CAAGCCTATGTCTGA[C/T]AGAGGGTGCACTCAA	154214
rs368695883	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078720	CTTTTGTGTGTGCAG[A/G]CGCATGTGTGCAAAT	154214
rs368740734	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038268	GCAGCAAAATATCTT[C/T]AAGTACATTAAGTAG	154214
rs368756397	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993819	GTAAAGAGTGTGTCA[A/G]GGCTAAGAGTGCCAC	154214
rs368769831	snp	C/T	3.48171e-05	0.00417221	intron-variant	RNF217	GRCh38.p7	6:125082439	AGATATTATTATCTG[C/T]ATTATACAGTTGAGG	154214
rs368847496	snp	C/G			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963684	ACAAGTTGTTGCCCT[C/G]CTCTTATTTCTTATA	154214
rs368848002	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125023260	AAAAGCATGCGGAGG[A/T]GCCCAGAGGCAAAAT	154214
rs368915794	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068322	TATGCTGTATTTAGA[A/G]TTCTCTCCCTACCTT	154214
rs368948843	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125040608	GCCAGCATCATCCTG[A/T]TTCCAAAACCTGGCA	154214
rs368988049	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125001518	TAGTAATTAAAATGT[G/T]ACAATTGAAATAATT	154214
rs369008862	in-del	-/TTTG			intron-variant	RNF217	GRCh38.p7	6:125024180	AGATGTAAATGATTG[-/TTTG]AAGAATTAATAAAGT	154214
rs369015034	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966876	TAGATGGTGACTTAA[A/G]TACCTCTATGCTCTG	154214
rs369039641	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086589	CATTAGATTATGTAC[A/G]ATTTAGTGATTTGGT	154214
rs369061175	in-del	-/A	0.0119091	0.0762411	intron-variant	RNF217	GRCh38.p7	6:125023417	TGGAGTTGTATGATC[-/A]GACTTGTGTTGTAAA	154214
rs369108534	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124989320	ACGTAGCAAAATAAT[C/T]CACACTCCATTGTGC	154214
rs369196250	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020636	AGTAAACATCTGTTC[C/T]GGGTAGGATTCTAGA	154214
rs369198456	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125047693	CAGTTAAGATCCTCA[G/T]ATCAACATCTTAAAT	154214
rs369216914	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125064292	AATCTGGAGCAGGGG[C/T]TATCATTGGCACTGT	154214
rs369297784	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125036218	TGCTGAGAATGATGG[C/T]TTCCAGCTTCATCCA	154214
rs369328892	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125060380	ACACACACACACACA[C/T]ATATATATTTGTACC	154214
rs369355745	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125066023	GCTCAGGCCAAGAAC[-/T]TTAGGTTATCCCAGA	154214
rs369364449	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125002089	CATTGAATTATTTTG[C/G]TATTGTTAGAGAGTA	154214
rs369366640	snp	C/T	0.00174932	0.0295229	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963010	GGTCAGCGGCGCCCG[C/T]CCCTCGCCAAGAGAC	154214
rs369368933	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125023998	TAAGTTCAAGCAACC[C/T]ATTGTACAGTATGGT	154214
rs369450299	snp	C/T	0.000193981	0.00984647	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009225	GAGAATCAAAGCTGT[C/T]GTATAATTAGTTCTC	154214
rs369451559	snp	A/T	0.000153988	0.00877328	intron-variant	RNF217	GRCh38.p7	6:125082587	CATAGTGTGCAAATG[A/T]TATGACTGTGGACAA	154214
rs369485883	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124968958	CATGAGATACTCTAT[A/C]AATGTATTAAATGTC	154214
rs369514653	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072620	GATATAAAATTACAG[G/T]GAAAATTATATGTGA	154214
rs369539314	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065947	TATGTTCTCTTCTCC[C/T]CAAAATGGTTCTTCT	154214
rs369552538	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997921	GAACTGTCCTTACCT[A/G]TTCTTATGTGACGGT	154214
rs369568913	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125074471	TTTTGAAATTCATAT[C/T]GTTCCATTAAATTGC	154214
rs369583390	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984172	AGGTACAAACAAATT[A/G]CTGGAACAGAGAAAA	154214
rs369597224	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125045116	CACAATCCTTTATTG[C/T]GGTCATGAAATAAGT	154214
rs369643257	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125030872	CTGTGTAGGGTCTCC[A/G]ACCCCACATTTTCCT	154214
rs369675190	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125027964	CATTGCCCATTTTTT[-/T]AATCAGATTATTAGA	154214
rs369691588	snp	A/G/T	3.48329e-05	0.00417316	intron-variant, missense	RNF217	GRCh38.p7	6:125082473	TTAAGACTTACTGGA[A/G/T]CCTCATAAGTGGTAG	154214
rs369701748	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124975228	TGTGGCAAGTTTAAT[C/T]ACCACAGCTTTTCCC	154214
rs369722262	snp	C/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961929	TGCGCGGGTGCCTGC[C/G]CGCGTGTGTACGTGT	154214
rs369759929	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031251	GGAGCTGCGATGAAG[A/G]CCTCTGACATGGCCT	154214
rs369783463	in-del	-/A			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961512	GGGTTAAAAAAAAAA[-/A]CTTCTAAGAGAACAC	154214
rs369785292	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125013390	GTGTGTGTGTGTGTG[-/C]TGTTTTTGAGAGCAT	154214
rs369788312	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125049964	AACATGACTCAGGAG[-/G]TGATTTGGTGGAAGT	154214
rs369798217	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125033772	GAGGAATCGCCACAC[C/T]GACTTCCACAATGGT	154214
rs369811513	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125008632	AGCCTTCCGTGGCTT[C/T]GTGCATTCAGGTCAG	154214
rs369830731	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076691	AAGGATGTGACCATA[C/T]GACCTGCTCACAATG	154214
rs369843702	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088723	TTTTTGTCACTTCCT[C/T]TTTTCTTCTAAAAAT	154214
rs369908302	snp	G/T	1.64939e-05	0.0028717	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076757	ACCGCCAGCTCCGAT[G/T]TTTTGGAGACCACAC	154214
rs369959340	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065861	AAGTTTTGGGGAACT[A/G]TGAGAAAAGCTATAT	154214
rs369965876	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124997981	ATGTCTGCCTGACTC[C/T]GGCATTCCTTTTCTG	154214
rs370046972	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961024	CCTCAGACACACATA[C/T]ATGATGGAAATGTTC	154214
rs370050775	snp	G/T	0.000299235	0.0122282	intron-variant	RNF217	GRCh38.p7	6:125045179	ATAACCAGTGACGTT[G/T]TTTTCCTTCCATCTG	154214
rs370087658	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985169	TGTGTACCAAGTGCT[A/G]GTTAGGATAGGGGAA	154214
rs370132767	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125008904	TCACCAAATTACTTT[C/T]CTATGCCACCAGCAA	154214
rs370138318	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125033813	TACAGTCCCACCAAC[A/T]GTGTAAAAGTGTTCC	154214
rs370203134	in-del	-/TTTC	0.0217236	0.101931	intron-variant	RNF217	GRCh38.p7	6:125061845	GATTAAAAGTTCAAT[-/TTTC]TTTCTTTATTTGATT	154214
rs370218512	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125069958	GTGCACCCATTATCC[A/G]AGCAGTGTACACTGT	154214
rs370252625	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006736	GGCGGATCACCTGAG[A/G]TCAGGAGTTCAAGAC	154214
rs370348157	snp	C/G/T	0.000492755	0.0156889	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962823	GGGACTGGCACTCAC[C/G/T]GGGCCTCTCAATCCC	154214
rs370352165	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124993219	ATTCCTGAGGTCTTG[A/C]CCCAAGAAATTCTGA	154214
rs370370457	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036554	AAGAGCTTCTGCACA[A/G]CAAAAGAAACTATCA	154214
rs370419265	snp	A/C/G	4.94632e-05	0.00497288	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009226	AGAATCAAAGCTGTT[A/C/G]TATAATTAGTTCTCT	154214
rs370447379	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083068	TCCCAGTGATTCTCC[A/G]TGGGCCACAATGCCT	154214
rs370455526	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091194	ACTGAAAATAAAGGA[A/G]GAAGTTGGTGAATAA	154214
rs370471562	snp	C/T	0.000153988	0.00877328	intron-variant	RNF217	GRCh38.p7	6:125082855	ACTTTAATTTTTTCT[C/T]ATCCCTAGGTTTATT	154214
rs370483789	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125055898	CTTCAACTTGTTTTC[C/T]TTTAAAAATGATTTA	154214
rs370491194	snp	A/G	0.0178098	0.0926698	intron-variant	RNF217	GRCh38.p7	6:125064806	TATACTTGTATGTAT[A/G]TACACATACATATTT	154214
rs370507959	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125054841	GTTTCCAACAAGTTC[G/T]CAGGTGATGCTGATG	154214
rs370518212	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048502	AGTAGGTTTGTATCT[A/G]CTGATAAAACCCTTG	154214
rs370571032	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086944	ATGACCAACTGTTCT[C/T]CTAAAATACCTATGA	154214
rs370595015	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090521	GTGTTTATCTGTTAT[G/T]ACTGTATATTCAGAA	154214
rs370635441	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124984580	AGAAAGAAAATAGAG[G/T]GGAGGGGAGGGGACA	154214
rs370689120	snp	A/G/T	2.1781e-05	0.00330001	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045482	TGGGTTAGATGTCAC[A/G/T]TGGCAGAAGCAGCCA	154214
rs370716145	snp	A/G/T	0.00123963	0.0248655	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009301	AAGTACATAGATGAA[A/G/T]AAGCCACATTTATTT	154214
rs370724799	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125026901	CACATGCAAAGAGTA[A/C]TTGTGTTTTGGATAC	154214
rs370777316	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987590	GCTCAGAAAATGTGT[C/T]TACTGCAAATTAGTG	154214
rs370785413	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998045	GCTCCTCAGATGCCT[C/T]AGATTATATATGTTC	154214
rs370794392	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125044723	TATTAGGCATTATAC[A/G]TTACAAAATCTTTTG	154214
rs370816324	in-del	-/T/TT			intron-variant	RNF217	GRCh38.p7	6:125008738	TTCCCAGGGGCTACC[-/T/TT]TTTTTTTTTTTTTTT	154214
rs370879440	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125033918	GGTATCTCATTGTGG[C/T]TTTGATTTGCATTTC	154214
rs370915356	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009625	TTCCCTCCCTTTCTC[C/T]CTCCTGCCCTTCCTT	154214
rs370918177	in-del	-/A	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125029663	GTAAATGTTGTTGGT[-/A]AAAAATGTAGAACGT	154214
rs370944829	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029141	TAATTACAAACTTTG[C/T]AGTAAGAGTTTGGAG	154214
rs371004017	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125066749	GCAGAGATTTGATCT[A/G]TTTTATTGTCTGAGT	154214
rs371105744	in-del	-/AATAT			intron-variant	RNF217	GRCh38.p7	6:124973567	TTGAAAATAAATTAT[-/AATAT]GTTTGCTATAAAAAG	154214
rs371152984	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124989514	GGTGGGAATCAATGA[C/G]AATGTCACCTATGAT	154214
rs371159639	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125020806	GAAAACAACAAATAA[A/T]TACTCTAACATATAT	154214
rs371162009	in-del	-/TAGA	0.495445	0.0475058	intron-variant	RNF217	GRCh38.p7	6:125074298	TAGACAGAAGATAGG[-/TAGA]TAGATAGATAGATAG	154214
rs371163623	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125000409	ATGATATGTTATATA[A/T]AATACACAATGTGTA	154214
rs371187513	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125013613	AGACTTATAGAGTTC[A/G]TATTCAGCTACCATA	154214
rs371224642	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090836	TTTATGCAATTTTAT[A/T]TTTTAACCTTTTCTC	154214
rs371240462	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125070672	TCTATTCATGTCCTT[C/T]GTCCACTTTTTTATG	154214
rs371258156	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057126	CCATTATTTTAAATG[C/T]TGCTTCATAGCAAAT	154214
rs371265247	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125027069	GGAATATATGAGCTG[-/T]TTTGATGTAAGCATG	154214
rs371266122	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125015507	GTAGGATGCCTGTAT[A/G]TGGAGGAACTTTAAG	154214
rs371283591	snp	A/T			intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971585	CTCAGCCTTCCGAGT[A/T]GTTGGGACTACAGGT	154214
rs371284324	snp	A/G	0.000153988	0.00877328	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081549	TTAGAATTATCTGAG[A/G]GCCATAGAGAGAATA	154214
rs371294363	snp	A/G	5.91862e-05	0.00543963	intron-variant, missense	RNF217	GRCh38.p7	6:125082460	ACAGTTGAGGAAATT[A/G]AGACTTACTGGAACC	154214
rs371305330	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125071694	ATCTTATGACCTTAA[C/G]TATAGAAAGATATAA	154214
rs371344962	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965959	GGTATATAACAGATG[A/G]GCAACTAAAACCTAC	154214
rs371356288	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125030077	CAAGAGAAAATGAAG[A/C]AGAAGCAAAAGCAGA	154214
rs371365464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979186	CCCTGTCTGCCTACA[A/G]ATTTGTCTGTCTCTT	154214
rs371411637	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125030032	CAGAATCATGGCGGG[A/T]GGTGAAAGGCATTTC	154214
rs371420255	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124978041	CATTAAAAAAATACT[C/G]AGCACAAAATATTTG	154214
rs371442306	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125075886	CTCACTGCTTGAGGC[A/G]GTGACTACCACACTG	154214
rs371476022	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125034115	TTGTCAGATGAGTAG[A/G]TTGCGAAAATTTTCT	154214
rs371499252	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125035197	CCTTTATTTCCTTCT[C/T]CTGCCTAATTGCCCT	154214
rs371518887	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033129	TTCAATATATCCAAG[A/G]CCATATAATTAATAC	154214
rs371522406	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125047617	TTGATTAGTAGAGGA[A/G]AAGAAAATTTGCTTT	154214
rs371535391	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125064085	GAAGTATTAATGTTG[A/C]ATCTTATAGGTATCC	154214
rs371599165	in-del	-/AGG	0.0170251	0.090679	intron-variant	RNF217	GRCh38.p7	6:124988017	GGAACCAGGCCACAT[-/AGG]AGGAGATAATGCTCG	154214
rs371604875	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086341	ATAAAATTTGAGGAG[A/T]TGTGTGTCAGATAAT	154214
rs371642530	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990550	CCAGTTGCTTAGACC[A/G]GAACTTTGGAATAAA	154214
rs371677071	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125052705	ATCAAGACTCATTTT[-/T]CTCCTCTCTATAACA	154214
rs371678257	snp	A/G/T			intron-variant	RNF217	GRCh38.p7	6:124991557	TGTCTTTTTCTCCCC[A/G/T]CAAGGCTGTAGGCCA	154214
rs371802727	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017552	TATCTTGGGGAAAGA[A/T]GACTTCTGTATAGAT	154214
rs371817771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072451	ATATTATTTGACCAA[C/T]GGTATTTTAGTTGCC	154214
rs371843918	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125059228	ACCTGGCTTTCTAAT[A/G]GAAGTGATGTCTAAA	154214
rs371901949	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124974382	ATTGGTAAATAACTT[C/T]GGTGGTGTGTTTTTT	154214
rs371919329	snp	A/G	4.95888e-05	0.00497915	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045297	TGTCTATAACTTAAC[A/G]CATGAAGACTCCATC	154214
rs371983328	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035356	AGATAGCTCTCTCTC[A/G]GCAGAAACTCTACAA	154214
rs372179285	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010729	TGCTTCTTTGTGCCT[A/G]CTACCCTATTACCCA	154214
rs372264798	snp	A/G	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125018153	CTTACTTTCAAATTA[A/G]CATTAATTAGAGGTA	154214
rs372311029	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125035321	CCCATTCAGTATGAT[A/G]TTGGCTGTGGGTTTG	154214
rs372376928	snp	G/T			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964273	ATTGTCCTAGGCCTA[G/T]TCATCTTTCAAAACC	154214
rs372379704	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125013159	GTTCATGGTTCTGGG[A/G]ATATAGCAGTTAACC	154214
rs372398538	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125030788	CTGTCGGTGGATGTA[A/C]CATTCTGGGGTCTGG	154214
rs372402419	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124987478	ATATAAACAGAATCA[A/T]GCAATATGTGGTCTT	154214
rs372424179	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125042417	ATTGCTAGAGCTGGT[A/C]GTGGGTAGGTATGGG	154214
rs372456171	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086285	TTAGCCAAATAAATA[C/T]CTTGCCAAAACTTAC	154214
rs372547588	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125060742	GAGCCACCACGCCAA[A/G]CCATATTTTGATTTC	154214
rs372558347	snp	C/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125077226	TATCCTCCACTCATT[C/G]ATGGAGGACCTGCAA	154214
rs372614743	in-del	-/TGAA			intron-variant	RNF217	GRCh38.p7	6:124977448	AAGATTATAAAATAA[-/TGAA]GCCAGTTCTAAAACA	154214
rs372662178	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125082698	GGAGAAAAGCTAAAG[A/G]GAAATATTAAAGAAT	154214
rs372670809	snp	C/G	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:124995895	TCATTGCACTCCAGC[C/G]TGGGTGATGAGCAAG	154214
rs372696342	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125035906	TTTTTCAATTTTACT[A/T]TTATTTATTTATTTT	154214
rs372708762	snp	A/G	0.000176597	0.00939508	missense, synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125082896	ATCTATTGCCTTTGT[A/G]AAAAACAGAGAAAAC	154214
rs372748228	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086368	TAATGTGAGAGAGAT[A/G]AATTGACTTTTGGAT	154214
rs372821605	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124998041	CATGGCTCCTCAGAT[C/G]CCTCAGATTATATAT	154214
rs372827055	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037421	TGTGTGTTTGGTATT[A/G]ATCACTTTTACTTGA	154214
rs372851290	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125047598	TAAACTCAATTGATT[C/G]CTTTTGATTAGTAGA	154214
rs372966144	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124969331	TTTGCTCAGTTTGTT[G/T]TGGATCATTCATGAC	154214
rs372979879	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054840	TGTTTCCAACAAGTT[C/T]TCAGGTGATGCTGAT	154214
rs373075172	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124979151	CTTGGCTTGAAGGTC[A/G]GGTTTCACCAAGGAC	154214
rs373110846	in-del	-/TGTGTA			intron-variant	RNF217	GRCh38.p7	6:125013346	GGTGCTTGCATGTTT[-/TGTGTA]TGTGTGTGTGTGTGT	154214
rs373174229	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009484	GGCAGAAAAAAAAAA[A/G]AAAAACAGAGACTAT	154214
rs373182508	in-del	-/A			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982026	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	154214
rs373205230	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124973391	CTCTGCCACCACTGT[A/G]TTTACCTCTTTTTAT	154214
rs373276187	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083600	CCCAGTAACCTTGTA[C/T]TTACCCAGTTCCATG	154214
rs373348182	in-del	-/TT			intron-variant	RNF217	GRCh38.p7	6:125004070	GGGGTTACAGTTTTT[-/TT]CTTTAAAATTCATCC	154214
rs373391925	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987992	CCAGGGATCAATCCC[C/T]GGACTGTTAGGAACC	154214
rs373435638	snp	A/G	8.24491e-05	0.0064201	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076805	TTGGATGCAAATATC[A/G]CTACCTCCCAGAGAG	154214
rs373450431	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125073691	AAAGCACTCTCTAGT[C/T]CAGCATCAGCCTAAG	154214
rs373542199	in-del	-/TT			intron-variant	RNF217	GRCh38.p7	6:125017155	ATATGTTTTGAAAAC[-/TT]TTTATGACACTGCCT	154214
rs373608764	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124988743	TAATTAAAGTTCTTT[A/C]ATCGTTAACACCTTT	154214
rs373610458	snp	A/G			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963754	AGAGACTGCCTCATC[A/G]GCCTGGTATCCCAGA	154214
rs373680190	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998623	GCCAACATGATGAAA[C/T]CCCATCTCTAACTAA	154214
rs373732851	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125026648	AAACATTTCTCTGAG[-/A]AAAAAAAAAGGGAAT	154214
rs373759966	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125059955	TTGGGTTCTGTGAAG[C/T]TTCTGTCTGTTTAAG	154214
rs373803000	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990015	ATTTCCTTTCTTTCC[A/G]TTTTCTCTTGAACCC	154214
rs373818003	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017045	CTGGACTTGGCCCCA[C/T]GCACCTTTTCTCTTT	154214
rs373835820	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124992223	CTCCTTTTAACATTT[C/T]AAGTAGGACATGTAT	154214
rs373861658	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125022162	GCTGGGATTACAGGC[C/T]TGCACCACCATGCCT	154214
rs373863730	snp	C/G	1.65285e-05	0.00287471	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045278	TCTTGGAAGAAACAA[C/G]TGTTGTCTATAACTT	154214
rs373864771	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125008855	TGGTGGAGAGATTTT[A/C]CTTATCAGCTCAATT	154214
rs373973100	snp	C/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982048	AAAAAAAAAAAAAAA[C/G]ATCTTGAGGCCCACA	154214
rs373981221	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999253	CATTTTTAATCTGCC[C/T]GTGTCATGAGTTTCT	154214
rs373987291	snp	A/G	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:124989391	TCTTTTGACGTATGC[A/G]ATAGTAATGAGAAAA	154214
rs373995376	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033644	ACTGTGAATAGTGCC[A/G]CAATAAACATATGTG	154214
rs374047493	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125067105	GCATGATGAAAGGTA[G/T]CCAGAAGAGGGAGAT	154214
rs374066842	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125031306	GGGATTAACATTAGG[C/T]TTCTTGCTGTGTATG	154214
rs374103686	snp	C/T	1.65108e-05	0.00287317	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076698	TGACCATATGACCTG[C/T]TCACAATGTAACACT	154214
rs374178321	multinucleotide-polymorphism	GC/TT			intron-variant	RNF217	GRCh38.p7	6:125031884	GTCCATTTTCACACT[GC/TT]TGACAAAGACATACA	154214
rs374178415	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022716	AAATAGTCCAGAACA[A/G]GATGCTGATTTTTCT	154214
rs374178865	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125033891	TGATTGCCATTCTAA[C/G]TGGTGTGAGATGGTA	154214
rs374182245	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125003349	ATAGGGATTAAAATC[A/C]CAGCACTGCTGGTTT	154214
rs374232477	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086338	AAAATAAAATTTGAG[A/G]AGATGTGTGTCAGAT	154214
rs374257508	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125025331	CAAATGGACAGATGA[C/T]AAGGACTGGAGACCA	154214
rs374330502	snp	A/G			downstream-variant-500B	RNF217	GRCh38.p7	6:125092794	AGGGTGTGCTTTTGG[A/G]AAGGTGGATTGTGTT	154214
rs374366348	snp	C/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967091	TTAGAGCTCTAAATC[C/G]AAGGCAGAGATAGTT	154214
rs374380201	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086342	TAAAATTTGAGGAGA[G/T]GTGTGTCAGATAATG	154214
rs374395307	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124993384	TTCTCCTCCCCTCCC[A/G]TCCTTTCCACTAAAA	154214
rs374401996	snp	C/T	0.0055096	0.0521962	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963191	TCCCAACGGATTCCC[C/T]CTCCCCCGACGGCGG	154214
rs374440655	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083256	TAAGAATTCTGAGCA[C/T]GCCTCTTCTGAGAAT	154214
rs374442078	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125057033	CAGGGCCACTATATT[G/T]ATATATTTCTAATAA	154214
rs374488228	snp	A/G	3.33189e-05	0.00408146	intron-variant	RNF217	GRCh38.p7	6:125082591	GTGTGCAAATGATAT[A/G]ACTGTGGACAATAAA	154214
rs374529466	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981473	TTTGGTTGGGGGGGC[A/G]GTGACTTTCAGGCCA	154214
rs374548958	in-del	-/GA			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961548	GCGAAGAAAAAGAGA[-/GA]AATTTTAAATTAGTT	154214
rs374569106	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092629	AAAGTTTTTAAAAGA[A/G]AAAATTCTTGTCTTT	154214
rs374570438	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125080000	TATCTCGTTCCTTCA[A/G]TTCTGTGATATTTGA	154214
rs374613765	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086773	AATTAAACACAAGTC[A/C]GGTTACAACATGATA	154214
rs374690031	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125063898	TGTCATGATATTTCC[C/T]TTTAGATATTTTATT	154214
rs374720538	snp	A/G	1.75068e-05	0.00295857	intron-variant	RNF217	GRCh38.p7	6:125057922	CCACTAGTAATTAAT[A/G]TGATTTTTTTCTTAC	154214
rs374727125	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125035042	TGATTTTTGTACATT[A/G]ATTTTGTATCCTGAG	154214
rs374743822	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016158	AAGTCTGTAAGCAAA[C/T]GTAACAACTTAATAA	154214
rs374838947	in-del	-/TGTGTG/TGTGTGTG			intron-variant	RNF217	GRCh38.p7	6:125052284	CCTTGTCATGCGTTT[-/TGTGTG/TGTGTGTG]TGTGTGTGTGTGTGT	154214
rs374848297	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124965963	TATAACAGATGGGCA[A/G]CTAAAACCTACTGAA	154214
rs374853624	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068725	TGAACAAAGTAATTA[C/T]TTGTTGAATGAAAAA	154214
rs374858047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013028	CTTGATTCTTCTTCA[A/G]TGCCCATAAGAAGAA	154214
rs374862637	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125081451	CTGGAAAATTATTCA[C/T]TGCACCTCTAATTAT	154214
rs374875408	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125040906	CAACATTCCTTCATG[A/T]TAACTCTCAATAAAT	154214
rs374950502	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023881	TAAAAAGTCAAACTC[A/T]TAGAAGCAGAAAGCA	154214
rs375006743	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037170	ATTGTTCTATTATCT[A/G]TCCTTGTGCCACTGT	154214
rs375019352	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966581	TTCTTTTAGTTTGTG[C/T]CACATAGTGCATTAT	154214
rs375031726	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007264	ATTTTTTTTTTTTTG[A/G]GATGGAGTTTCCCTC	154214
rs375063940	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973657	TAGATTGGTGCAAAA[A/G]TAATGGCAGAAACCC	154214
rs375088431	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088712	GCCATTGCCCTTTTT[C/T]GTCACTTCCTTTTTT	154214
rs375115917	snp	A/G	0.00029074	0.0120534	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963102	GCTCTCGCCGCCCGC[A/G]TCGCCACCTGGGGCT	154214
rs375132115	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087367	GTGAGTCTTCACATT[C/G]GATTATATTTTTATT	154214
rs375177942	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125058481	AATTATATAGGCTTT[A/G]AATCCTTGCGATCTT	154214
rs375186638	snp	C/T	0.0105592	0.0718895	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963075	CCTGCCCGAGGCCCC[C/T]GCCTCGGAGCAGCTC	154214
rs375187109	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998772	CACTGCACTCCAACC[C/T]GGGCAACAGAGCGAG	154214
rs375214242	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042488	AGGTCTTTGGTTCAG[C/T]GTAGTAGGATAGGGA	154214
rs375242775	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979359	GTTAGGCGTGGGCAG[C/T]TCTCTAAGTGAGCAA	154214
rs375278633	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091015	GGAAAAATTACGTTG[A/G]GATGAAATGTTGAGA	154214
rs375370351	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125034166	TTCATTCTGATGGTA[A/G]TTTCTTTTGCTGTGC	154214
rs375377662	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987720	GGCTCAAGTGATCCT[C/T]CTGCCTCAACCCGTG	154214
rs375390994	in-del	-/TGTGTGTG			intron-variant	RNF217	GRCh38.p7	6:125071485	GCATCTGCCTACATA[-/TGTGTGTG]TGTGTGTGTGTGTGT	154214
rs375412836	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969016	GGCAGTATTTTCCCC[A/G]GCTTTATCTGATGGC	154214
rs375413845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032053	AACCCATCAGATCTC[A/G]TGAGACTTATTCATT	154214
rs375517354	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125018268	CATTTGAGGAAAGTT[A/G]ACAATTATCTTTATT	154214
rs375526100	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031293	ACTCATGATCTTGGG[A/G]ATTAACATTAGGCTT	154214
rs375533752	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077204	ATCCAGCAGCAGGTC[A/G]TACACATATCCTCCA	154214
rs375576919	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125044325	TATTGTTCACTACTT[-/A]ACGAAAAATACTCTA	154214
rs375622929	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125019831	GTCCCCTTTTTTGCA[-/G]GTGGGGGGGGAGTGA	154214
rs375641183	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125003972	TGTTGTCCAGTAGCC[-/T]AAATGATGTCAAGTG	154214
rs375657513	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125066119	TATTTAGAATCTGAC[C/T]ATATCTCAGTACCCC	154214
rs375729913	snp	A/G	0.153332	0.230554	intron-variant	RNF217	GRCh38.p7	6:125034515	AGTTGTAGATATGCG[A/G]CATTATTTCTGAGGG	154214
rs375734619	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074990	CAATAAAATTTCTAA[A/G]CAAAGAACTCACATG	154214
rs375760261	in-del	-/AC	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125000378	GTTACACTTTGAGAA[-/AC]ACACATAATGTTATA	154214
rs375827906	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125033864	AGCACCTGTTGTTTC[C/T]TGACTTTTTAATGAT	154214
rs375841758	snp	A/C			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009489	AAAAAAAAAAGAAAA[A/C]CAGAGACTATTTACC	154214
rs375843348	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125014579	ACTGTAGCTGGAGTA[A/G]TCAGCCTCCAGAGAT	154214
rs375850430	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124970798	AAAGAGTCTAAAAGG[C/G]AGTGGGCTAATTCGG	154214
rs375878922	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986631	TCAAAAGAATTTTAT[A/G]AGGTTATCTCTTCCC	154214
rs376006531	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088147	AGCACGTGCCTACTA[C/T]GCCTGTCTTCAAAAT	154214
rs376044168	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036497	GATCCAAAAGGAATC[A/G]CAACAAAAGCCAAAG	154214
rs376044746	snp	G/T			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963737	CTCAAAGGAGGAGAG[G/T]AAGAGACTGCCTCAT	154214
rs376167308	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125056163	GTCAAAGAACAAATG[C/T]CGTTTAGTATAAGAC	154214
rs376197445	in-del	-/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125050773	GAATCTAGTTGTGCG[-/T]TCTTCCCTGCAAGGT	154214
rs376199682	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125058683	TCAAGAACTAGCAGG[A/C]AATTTGAGCTCAGAC	154214
rs376212216	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125026271	CCAGGCTCTGCCAGT[G/T]ACTAACATTGAATTA	154214
rs376223558	snp	A/G	5.2946e-05	0.00514492	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082912	AAAAACAGAGAAAAC[A/G]ATCACGGACAGGTAT	154214
rs376235244	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029677	GTAAAAATGTAGAAC[A/G]TGCATTTTTTAAAGT	154214
rs376244004	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124998005	TTTTCTGATTGTGAG[A/C]AAGGGGCATCTCCTA	154214
rs376248210	snp	A/T	3.39219e-05	0.00411823	intron-variant, synonymous-codon	RNF217	GRCh38.p7	6:125082480	TTACTGGAACCTCAT[A/T]AGTGGTAGAACCAGG	154214
rs376258075	in-del	-/AAGTTTAGGTTC			intron-variant	RNF217	GRCh38.p7	6:124997019	TTGTAGCACTCCTGC[-/AAGTTTAGGTTC]TACAAACACGGACGT	154214
rs376281714	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086600	GTACGATTTAGTGAT[G/T]TGGTGGGATAATTAT	154214
rs376283130	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054104	CAAACACAGTTCACT[A/G]AGGAGTGAACTTGTG	154214
rs376367793	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125031299	GATCTTGGGGATTAA[C/T]ATTAGGCTTCTTGCT	154214
rs376433554	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125059536	TTTATATCCTTTGGA[A/G]AGCTGTAAAAACAAT	154214
rs376452948	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124983464	GAGTGATGGTTTAGT[A/G]GATTTATGTCCTCAC	154214
rs376515955	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965956	TCTGGTATATAACAG[A/G]TGGGCAACTAAAACC	154214
rs376532573	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125066466	CTGCAGGTATTCTCC[C/T]TTCTCAGGATCTCAG	154214
rs376560387	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124989877	TGCTTGAAAAAAAAA[A/C]CACCAACAAAATAAA	154214
rs376582435	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124991602	TTGTTTGGTTTTGTT[C/G]ATTCATGAGGCCTGA	154214
rs376590588	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125013410	TTTGAGAGCATGGTC[A/G]TGGAACGGTTCATTG	154214
rs376599824	in-del	-/TAGATAGATAGATAGATAGA			intron-variant	RNF217	GRCh38.p7	6:125074298	TAGACAGAAGATAGG[-/TAGATAGATAGATAGATAGA]TAGATAGATAGATAG	154214
rs376604065	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009937	TTGGTTCATGCTTGT[C/T]GTTTTCTGTTCCCTT	154214
rs376760580	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124978654	CTCCTTTATTCTCGT[C/T]GCCCACAGCTCAGTG	154214
rs376762246	in-del	-/AGTCAAG			intron-variant	RNF217	GRCh38.p7	6:124970426	GGATGAGAGAAAAAG[-/AGTCAAG]CATGAGTCAGGTTCT	154214
rs376827046	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124994055	GGGACTGGAAAGAGG[C/G]AAGGGGTCATGATGG	154214
rs376883431	snp	A/T	1.80964e-05	0.00300797	intron-variant	RNF217	GRCh38.p7	6:125045166	AAAATGAAAGAAAAT[A/T]ACCAGTGACGTTTTT	154214
rs376896841	snp	A/G	0.0130921	0.0798413	intron-variant	RNF217	GRCh38.p7	6:125028423	ATTAGGCTATTATAT[A/G]TTTCTTTTGGAACTA	154214
rs376914394	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125069927	AAATTCTTTAGTGGT[C/G]ATTTCTGAGATTATA	154214
rs376939792	snp	G/T			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006099	AATGATAAGAGGCTT[G/T]AGGATACTTCCCAGG	154214
rs376951877	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125028006	AGGGTTGTTTGGACT[A/C]CTTATATATTCTGGT	154214
rs376954912	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124984865	GGGGAAAATGATACT[A/G]TAAACTGAGACAAAA	154214
rs377043627	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125073139	AGTCAAAAAGTTGAA[C/T]GTACGATGCTTTGGG	154214
rs377062378	snp	A/G	1.66211e-05	0.00288275	intron-variant	RNF217	GRCh38.p7	6:125082573	ACAAGTGTGAGTATC[A/G]TAGTGTGCAAATGAT	154214
rs377065733	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125082672	ACTGGTATCACTGAG[C/G]GTGCTAAAGGGGAGA	154214
rs377073738	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048458	TCTGTGCAATTTAAC[A/G]TCTCTTTATAATAAT	154214
rs377144215	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125004745	CAAGAACCACAGCTC[G/T]TGTGTAATTCTGGTG	154214
rs377167236	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124973187	GCTTCACATAGAGAT[C/G]CCAGCTCATAACACT	154214
rs377187171	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124974503	TTAGGTAGTTCCACT[A/G]TAATTGAAATACGTC	154214
rs377199544	snp	C/T	9.46119e-05	0.00687728	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082949	GTAACATGCAGATGA[C/T]TTCATCCAGCTAAGC	154214
rs377220657	in-del	-/A	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125030837	TTGCAGCTCCACTAG[-/A]CGGTGCCCCAATAGG	154214
rs377246064	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013972	CAAGTTATACTGTCA[C/T]CCTGTCTCTGTTTAT	154214
rs377308768	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124984562	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAATAG	154214
rs377325472	snp	A/C	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089173	CCTAGCCCTCTGCCA[A/C]GAAGTAAGTCAAGCA	154214
rs377332890	snp	A/T	0.000143895	0.00848097	intron-variant	RNF217	GRCh38.p7	6:125082424	AGGACATTATGTAAT[A/T]GATATTATTATCTGT	154214
rs377368734	snp	A/G	0.000153988	0.00877327	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045460	GTAAGCATTTTCACC[A/G]GAGCTGTGGGTTAGA	154214
rs377371751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978064	AATATTTGCTTAGCA[C/T]CATGCTAATCATTAT	154214
rs377414457	snp	A/G	3.30049e-05	0.00406219	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076851	ATTAGTGCGAGGGTC[A/G]GTCTGTGGTGAGTGT	154214
rs377442851	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961409	GTTATGCTAATGAAA[C/T]TGCCCATGATTTCCA	154214
rs377475254	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077167	GAGGGGCAGTGTCAT[A/G]TATATTTTTGTAATG	154214
rs377492149	snp	A/C			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962279	CGCCCGAGCCCAGAG[A/C]GAGCGGCCCTCGGCG	154214
rs377543177	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124978128	TCCATGGTCCAGCTT[C/T]TTAGAAACTTTAGAG	154214
rs377571577	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125010952	AAAAAGACGGGGTTG[A/C]ATTCAGTTATAACCT	154214
rs377610273	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092442	AGTAATCTTAATTAT[G/T]AAATCAGATTGCATG	154214
rs377619298	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980676	TTTGATCGTGCCTGT[C/T]CTTTTCTTTGTTTTT	154214
rs377649175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977900	CTTCCACTGGCTAAG[A/G]CTTTCCTTCTTTTTA	154214
rs377688310	snp	G/T	0.00953873	0.0683987	intron-variant	RNF217	GRCh38.p7	6:125035022	TTGGTGTATAAGAAT[G/T]CTTGTGATTTTTGTA	154214
rs377728289	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084097	GTTATCTCTTGCCTC[C/G]TCCTCTCTGTTTTTA	154214
rs377740641	snp	A/C	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967550	AGTGCTAGAGATTGG[A/C]AGATGCATATAACTT	154214
rs377750449	snp	A/G	4.94849e-05	0.00497393	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076754	GATACCGCCAGCTCC[A/G]ATTTTTTGGAGACCA	154214
rs386408518	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125066996	AGTGGAATGTTGCAG[-/G]GAGTATTATACGAGG	154214
rs386705545	multinucleotide-polymorphism	AGA/GGC			intron-variant	RNF217	GRCh38.p7	6:125037953	TAAATTGAGCAATGA[AGA/GGC]CTGAGATTTGTACTT	154214
rs386705547	multinucleotide-polymorphism	AGA/GGG			intron-variant	RNF217	GRCh38.p7	6:125050155	GGTAGGTGCAATTCT[AGA/GGG]TTTCATTCTTATTCC	154214
rs397723175	in-del	-/CA	0.5	0	intron-variant	RNF217	GRCh38.p7	6:125060380	ACACACACACACACA[-/CA]TATATATTTGTACCC	154214
rs397733365	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125001892	TTACTCCCATCAATT[-/T]ATTCCCTGACAGATG	154214
rs397816787	in-del	-/A	0	0	intron-variant	RNF217	GRCh38.p7	6:125004071	GGATGAATTTTAAAG[-/A]AAAAAAACTGTAACC	154214
rs397828516	in-del	-/A			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964442	CTGGACAATGTCTTA[-/A]GAGTCCCATATGTGG	154214
rs397885401	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125024740	AAAAAAAAAAAAAAA[-/A]TGAAAGTGGGCAGTC	154214
rs397885745	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125007262	CATTTTTTTTTTTTT[-/T]GAGATGGAGTTTCCC	154214
rs397886159	in-del	-/AG			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961547	GGCGAAGAAAAAGAG[-/AG]AAATTTTAAATTAGT	154214
rs397886174	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125044069	TTTAGTTTTTTTTTT[-/T]AATTGCTTTTTGTAG	154214
rs397886328	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124985473	TCTTAGTTATTTTGG[-/G]AAGTGAATTTCTATC	154214
rs397887738	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125045154	TATACAAAAAAAAAA[-/A]TGAAAGAAAATAACC	154214
rs398002780	in-del	-/CA	0	0	intron-variant	RNF217	GRCh38.p7	6:125013388	TGCTCTCAAAAACAG[-/CA]CACACACACACACAC	154214
rs527246879	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125070789	TGAAGGAAACACATA[C/T]ATAAAAATACTTTCA	154214
rs527247702	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979503	AACAAAGATACCAGC[A/G]TGGCGCAGAGCACCA	154214
rs527253360	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003726	TTATTTGTCAATTTT[A/G]AAAATACAGGTAGTT	154214
rs527283382	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125013566	AAAAAAAAAAAAGTA[A/G]TCTGAAAGCTTTGGC	154214
rs527290905	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996741	TATAAGTCACAACAA[C/T]TACAAATTTTAAAAG	154214
rs527312310	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004603	GTTGGGATAGTATCA[C/T]TGGGAGAAGAACAAG	154214
rs527325753	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045855	TAAATGGTACTCATT[C/G]ATTTATTCAGCAAAT	154214
rs527363411	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088613	TTACAAACTATATAT[A/G]TCTTTTTGGCTAGAG	154214
rs527371458	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989623	CCAATAAAGCTTTAT[A/T]TGTAAACACTTAAAT	154214
rs527389170	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038571	GGATTCATAATACCC[A/C]TCTGCCAACCTTCAC	154214
rs527432177	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125080527	TTGCCTTGTGAGTCT[A/G]CTGCAAAGTTTCTCT	154214
rs527451405	snp	A/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125031995	TGAAAGGCACTCCTT[A/T]CATGGCAGCAGCAAG	154214
rs527511124	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125032787	GAGGATAAGGGAGCA[C/T]GAACATTCAGATAGT	154214
rs527520813	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125026048	AGCCCATATGATCGT[A/G]GAGACCATCTGCTTG	154214
rs527580090	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019357	ACTTACAACTCTGCT[A/C/G]TCTTTCTTACCATTT	154214
rs527620041	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125067939	AAAGATGTCACTGAA[A/G]CAATAGTGTATCAAA	154214
rs527631628	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124969112	TTTATTAAGCCAGTT[C/T]TGGGACACCAGCTAA	154214
rs527637401	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019932	CTGTTTGCCTCTTAG[C/T]TTAGTCAGCTTTGTG	154214
rs527786692	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005779	GAAAGCTTTCAAATA[G/T]AGACTTGTTTAATTA	154214
rs527799953	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046986	TGCCCTACAGTGGTG[C/T]TGAAGGCTAACTGAA	154214
rs527872642	in-del	-/A	0.0123305	0.0775448	intron-variant	RNF217	GRCh38.p7	6:125019836	CTTTTTTGCAGTGGG[-/A]GGGGGAGTGAAAAAA	154214
rs527887402	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124998756	CAGTGAGCCATCGCA[C/T]CACTGCACTCCAACC	154214
rs527900661	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090333	AGAAGGAACACAACA[A/G]TGATGTTAAAATGTT	154214
rs527916138	in-del	-/T	0.154024	0.230843	intron-variant	RNF217	GRCh38.p7	6:125004066	TGAGGGGTTACAGTT[-/T]TTTTTCTTTAAAATT	154214
rs527974339	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124991477	CTTGTTTAATCTGCT[G/T]TATTTTTTCATGGCT	154214
rs527979717	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125040734	CACATCAAAAAGCTT[A/G]TCCACCACGATCAAG	154214
rs528023457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075047	AAGTACCTACTCCAA[A/G]TGCAAGCTTGTCCAA	154214
rs528055145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027522	ATAGTACTCCATTGT[A/G]TATATGTACCACATT	154214
rs528059397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034448	CACCATTTATTAAAT[A/G]GGGAATCCTTTCCCC	154214
rs528122255	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028240	TGGTTCAGTACCCCT[C/T]TAAATATATGACAAA	154214
rs528164881	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069520	GTAGTATTCCATGAT[C/T]TATATATACCACATT	154214
rs528195837	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125026859	AAAATGAACTGTGAT[A/G]TACTAGTTATAGAGT	154214
rs528212249	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125070082	ATAGCTTAGCTCCCA[C/T]TTATAATTGAGACCA	154214
rs528219160	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124968934	TTGGGGTACCTGTAT[A/G]ATAAGCACCATGAGA	154214
rs528232418	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971433	AAGCTATGATTTGAT[A/T]TGATTTACTGTTAAG	154214
rs528254332	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971750	TGAGCCACGGCACCC[A/G]GCCGATTTACTGTTA	154214
rs528257439	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965636	AGATGAGTCATAGAT[A/G]CCGGGCATGCTTTCA	154214
rs528275723	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001126	TGATTAATACCACCT[A/G]CTGCTGATTTATGAG	154214
rs528283540	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125007315	CAGTGGTGCGATCTC[A/G]GCTCACCGCAACCTC	154214
rs528289227	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125015341	TTTTTAAAAGTTCGT[A/G]CTTGTAAAGTCAGCA	154214
rs528292650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063621	GATTTTCAGTGTACC[A/G]CTCAGATCATCACTA	154214
rs528292950	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055585	CTAATATTTCATAAA[G/T]ATAATCTAAGACTGA	154214
rs528293699	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998575	GAGGCCAAGGTGGGC[A/G]GATCATGAGGTCAGG	154214
rs528334230	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027784	CAAAAGTGTACAAAG[A/G]TTCCCTTTTCTCCAT	154214
rs528346756	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125007876	TTAATACATATATAC[C/T]TCTTATAAAGTGTAA	154214
rs528355932	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056336	TATCTACCTTCCAGC[A/T]TTATTTTGAGGATGA	154214
rs528408149	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125000245	TTTGTTTGCGATTCT[A/C]GAAACTAAAAATGTA	154214
rs528440495	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091966	TATCATAATATATAA[C/T]TCAACTTTTCCTGAT	154214
rs528464401	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041738	CACAGGTTACAATCT[A/G]TCTTGTTTATTTGCT	154214
rs528477308	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977233	AATGTACTAGCTGAA[C/T]TTCAGCCACAACCTT	154214
rs528493955	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092774	CAGGAATGAACAGAA[A/T]TTCAAGGGTGTGCTT	154214
rs528507978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008850	GTAGCTGGTGGAGAG[A/G]TTTTCCTTATCAGCT	154214
rs528511800	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993366	ACAAGTAAATATTAG[A/T]TCTTCTCCTCCCCTC	154214
rs528515569	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042337	ACACTTTAAGAGACT[C/T]ATATCCATTGTTCCA	154214
rs528516969	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124974104	TGGAAGCTGCATGAC[A/G]TTTTCTGCCCTAAGT	154214
rs528524233	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124980986	AACATAAACTCTGTA[C/T]GTTTGTTTAATTACT	154214
rs528539869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993837	CTAAGAGTGCCACAG[C/T]TGAAAGAGCATACTT	154214
rs528555164	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125043159	AGTCTGCTGTTCATC[-/T]TTAAGAGCCGTCCCA	154214
rs528568869	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125036000	TGCCATGGTGGTTTG[C/T]TGCACCCATCAACCC	154214
rs528580059	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084718	TGTCTATTTCCAGTT[A/G]GAGGAGTGTGTGACA	154214
rs528603642	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987369	ATACCCATTATTCAT[C/T]ATTCCCTGCCCTCAC	154214
rs528626944	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036041	CTTTAAGCCCCGCAT[A/G]CGATAGTTATTTCTC	154214
rs528630528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030024	GGAGGCCTCAGAATC[A/G]TGGCGGGAGGTGAAA	154214
rs528680766	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125002571	CAAAGAATTTTTTTA[A/T]CCTTATTATCTACGA	154214
rs528706101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077877	ATGACTGTTGTGAAC[C/T]ATTTTCCTCCTTAGA	154214
rs528753606	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071199	TTCGACTTTTCTTAC[A/G]ATTTTTCAACTTTTC	154214
rs528768117	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023445	AAAAAGAGTGCTCCA[G/T]AGAAGAGGGCACCCT	154214
rs528771086	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016021	TGTCAATGGATTCAC[A/T]GGTACATAAAAATAT	154214
rs528814482	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125052392	TTTAGGAAAGTTTCT[C/T]TTTCCCTTTCCAGCT	154214
rs528822160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965866	CATACTCTGTCTTAC[A/G]CTTAAGTAATTAAGT	154214
rs528834697	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124973539	AAATATTTGTTAAAG[C/T]CTGAATGAATGATTG	154214
rs528845396	in-del	-/AAG			cds-indel, nc-transcript-variant	RNF217	GRCh38.p7	6:125091034	GAAATGTTGAGAAAT[-/AAG]GAGTATCTTAAAAAC	154214
rs528863753	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124966314	TAATTTCCTCATCAA[A/T]GAAATGTAATTGCAG	154214
rs528912422	snp	C/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009371	TGTGAAGCCCTCTCA[C/G]AGACATAGAGCCTGG	154214
rs528917549	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058441	TATAAGTTCTAGTCT[C/G]CCACGTGTACTATAA	154214
rs528970610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050938	GCCCTGTTGATAGAC[A/G]CCAGTGTAAACAAAG	154214
rs528970726	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088550	TATCACATACCTTAC[A/G]AAATCCCTATACATA	154214
rs528997414	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125043233	ATACAAGTTGATCCA[A/G]TTGGGGTATGCTAGT	154214
rs529037267	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002833	TCTATTATAGCTAGA[C/T]GAAGGAGAGACTCTT	154214
rs529070461	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086849	CTTGTCAGAAAATAC[C/T]TTGTTCTGTGACTCT	154214
rs529164184	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125008061	GTAGATCAAGACCAT[-/C]CCGGCTGACATGGTG	154214
rs529188143	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037737	TGCTTTGCTTGTAGT[A/T]GATCTATGTATATTT	154214
rs529189763	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079594	TTAACTTGATAAGAC[A/C]TCTGCTAACTATTGA	154214
rs529197762	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124981266	AACTGGAATTTTTCC[A/C]CATGTGAACACAAAA	154214
rs529203008	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030935	GGCCCTGCCCCTGCA[A/G]CACACTTTTGCCTGG	154214
rs529226527	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071949	CAGAGCTAAACTCAT[C/G]AATATTTTTGGAGCT	154214
rs529272932	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072585	AGATTTTAGAACCCA[A/G]TGAAGCAATATTACA	154214
rs529300920	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125049746	GCAACCCTGGGTATT[A/G]AGAAGGGCATGGGGG	154214
rs529319901	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975382	AATCACAGGTGACTC[G/T]GATATGGCCAGATTG	154214
rs529323068	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977647	AGGGTGGTAAGGAGG[C/T]CAAGGTCAAGCAGGC	154214
rs529332712	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125066404	GTCATATCTTTCCTT[C/T]CTTCACCCTGCTACA	154214
rs529336307	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025318	TTTGGCTTGGCTGCA[A/G]ATGGACAGATGATAA	154214
rs529361256	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018054	CCATTTCTAACACTA[G/T]CTATTCAATAATTTG	154214
rs529377718	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967968	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	154214
rs529421459	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125011693	TTCTAAAAAAGTCAC[C/G]TTTAATTTTTTTAAA	154214
rs529433539	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059340	TCAGATCACTGCATC[A/G]GTTGCTCAGTATACT	154214
rs529436550	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009579	CTGACTATTCTATTG[C/T]ATTAGAATTATAGGC	154214
rs529460887	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960606	ATGTGTGTGAGGAGG[C/G]GTTCCCAAAACTATA	154214
rs529461797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003991	TGATGTCAAGTGCTG[C/T]AAAAATCTGCACCTA	154214
rs529468946	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124968943	CTGTATGATAAGCAC[C/T]ATGAGATACTCTATA	154214
rs529504362	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012220	TTTAAAATATAGCAT[A/T]TACAATACTAAAAAT	154214
rs529521290	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004688	ACTTGTTGTTGAAAG[A/G]GAAAGTTAAAATTAT	154214
rs529550151	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998665	ACCTAGTGAAGCATG[A/G]TGGCGTGCACCTGTA	154214
rs529557576	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961527	ACTTCTAAGAGAACA[C/T]TGTAGGCGAAGAAAA	154214
rs529573716	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125046029	AAAGCTGTGTACATA[C/T]AGTGTGCTTTGAGGA	154214
rs529577378	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125033241	GGTACATGTGCACAA[C/T]GTGCAGGTTAGTTAC	154214
rs529577398	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997638	CATCTGACGCATTGA[A/G]CACATTCATAGGTCC	154214
rs529617479	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124976775	CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC	154214
rs529634215	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125038733	TGAAGGCAGGATTCA[C/T]GGCTTAATTCACTTT	154214
rs529663381	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997982	TGTCTGCCTGACTCC[A/G/T]GCATTCCTTTTCTGA	154214
rs529677015	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124995969	TTTGGAATATTTCTG[G/T]GTTTTTTTTTTCTAT	154214
rs529679174	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990146	GACTTCAAGGACACC[A/G]TAGTCTTCATTTTCT	154214
rs529750395	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993648	CCTGTCTTACAGTGT[A/G]GTAGGTGCTACATTA	154214
rs529755635	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990802	GGGCATGGTGGCTTA[C/T]GTCCGTAATCCCAGC	154214
rs529788504	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001038	CCAATCACCAGCTCA[A/G]AGATTATGTTTTACT	154214
rs529852084	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068048	TATTTTGCAGATGGG[C/G]GTCATGGATAATATT	154214
rs529876263	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019971	CCCAGTAACCCTGGG[C/T]GAGGGACTCCAGGTG	154214
rs529911144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125061655	AATTAATTGATTTGC[A/G]TATGTATTGTTTAGT	154214
rs529939712	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013293	AAAAACAAAGCTAAC[A/G]TAAGAGGAAGGGTAG	154214
rs529969789	snp	A/C			missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076779	AGACCACACATCAAA[A/C]CTCAGTATATTTGGA	154214
rs529969805	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044836	TTTGGCATGTTGTCT[A/G]AATGCTGCCTGACCC	154214
rs529990036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977859	TTATTAGGGAGTTGC[A/G]GAGATTTTACATAGA	154214
rs530084917	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125056847	GAGTGGAAATAATGT[G/T]TATGAGTGGAATATT	154214
rs530115514	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007106	ATTTTGTCTTCAGCT[C/G]TATCTAGTCTATAAA	154214
rs530124085	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006680	TGGGCTGGGTGTGGT[G/T]GCTCATGCCTGTAAT	154214
rs530130492	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125047279	TTAAATGTGTTGTTT[C/T]TATGAAATGGGTAAA	154214
rs530147047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028024	TATATATTCTGGTGA[C/T]TAATTTCTTATCAGA	154214
rs530160511	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040338	ATAAACCAGAAAATC[C/T]AGAAGAAATGGATAA	154214
rs530172670	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125066368	GCCCTCTGGACATGT[C/T]CCCACTCTGTGACTC	154214
rs530251808	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999230	TTCCTCTTGTAGGAA[C/T]GTCATTCCATTTTTA	154214
rs530265625	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090961	ATTTTTTAATTAGAC[A/G]ATGTTGATATGCAGA	154214
rs530300677	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040895	TCGATAAAATTCAAC[A/G]TTCCTTCATGTTAAC	154214
rs530308841	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083434	CCCAGCAGTATAATT[A/C]TTTTATCTTTCAAAT	154214
rs530310269	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125075995	GTGAACTACCCAAAA[A/C]TGAAATCCTTGTTAC	154214
rs530330430	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125035086	TGCTTATCAGCTTAA[A/G]GAGATTTTGGGCAGA	154214
rs530411045	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125026688	GTGCTATACAAGTCA[A/G]CTTTTTTTAGGTAGG	154214
rs530411525	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124978932	CTGTGTGGCTGAGTC[C/T]AAGGTTTTTATGGGC	154214
rs530411985	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971499	TCTCACTCTGTCACC[A/G]GGCTGGAGTGCAGTG	154214
rs530425816	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070174	CCAAGTTTCTGCAAA[A/G]GACATTATTTCATTT	154214
rs530435301	in-del	-/AT/CA			intron-variant	RNF217	GRCh38.p7	6:125060381	ACACACACACACACA[-/AT/CA]TATATATTTGTACCC	154214
rs530437085	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B, missense, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964798	CCTCAAAACAGATTT[C/T]GCTGCCCTGCGATGG	154214
rs530483331	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125029376	ATAAAGGAAAATATG[G/T]TTCCTCTACACTAAA	154214
rs530491562	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971906	CTCTTCTCACTTTGT[A/G]TACTGTTAGTGGGGC	154214
rs530509679	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029244	CCCCTAGAATGAGTT[C/T]GTTTTCTCCCTATTT	154214
rs530526681	snp	C/T	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:124973141	TCAGTATTTCATTTT[C/T]TTGTTTAAAAACCTG	154214
rs530547453	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064404	CATTGTATCCAATGC[C/T]CTGTTTTTATGACAA	154214
rs530550171	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022040	GCATGCACCACCACA[A/C]CTGGCTAATTTGTGT	154214
rs530554668	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062503	TATTTTTATGAAAAC[A/G]TAACCCACCACATTA	154214
rs530607738	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057182	TGTGTTTTTATTGTT[A/G]TTGTTGTTGTTTTGA	154214
rs530609154	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027353	CTACTCTCTATGTCC[A/G]TGAGTTCAATTGATG	154214
rs530609186	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124996336	TTTTGAAGATAATTT[A/T]TGTTTTCTCTGATGT	154214
rs530614642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965470	CCCAGCTACTTGGAA[A/G]GCTGAGGCAGAAGAA	154214
rs530621775	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015387	TCTACGAAAATAATC[A/C]GAAATGCCCACAAAC	154214
rs530644496	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025809	AAGGGATATTTACAA[A/G]TGTACTCTCTTATGA	154214
rs530657191	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056423	AATAAATAAATAAAC[A/G]TGAAAATCTTTTAAG	154214
rs530680610	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125023886	AGTCAAACTCATAGA[A/G]GCAGAAAGCAGAATG	154214
rs530695868	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000992	AGTGAAAACATTCTA[A/C]AATGACCTTGGAATA	154214
rs530745607	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124993983	CAGTGATTGAAAGTC[A/C]TTGAAACAACATTTT	154214
rs530834809	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994486	TGCCTCATGAATGGT[A/G]GACTTCACAAACTTG	154214
rs530848887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042477	AATAAAATATGAGGT[C/T]TTTGGTTCAGTGTAG	154214
rs530868318	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988034	GAGGAGATAATGCTC[A/C/G]GGTGAGCGAGCATTA	154214
rs530890362	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124990016	TTTCCTTTCTTTCCA[G/T]TTTCTCTTGAACCCA	154214
rs530900953	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125037976	ATTTGTACTTTTTCC[C/T]GTCCTTTTCTTTGGA	154214
rs530908171	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032788	AGGATAAGGGAGCAC[A/G]AACATTCAGATAGTA	154214
rs530908827	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057363	ATTTTTATATTTTTC[A/G]TAGAGATGGGGTTTC	154214
rs530917562	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125005623	CTTTTTTCTTAAATC[C/T]ATACCTTTGAAATCT	154214
rs530918977	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030402	AAAATCCCATCTGAG[A/C]CAAGGCAACTCCCTT	154214
rs530920490	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125036025	CAACCCGTCATCTAG[A/G]CTTTAAGCCCCGCAT	154214
rs530952756	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124980190	CTGGCCAAAAAATTT[G/T]GAAACATCTTTTGCG	154214
rs530954380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002287	CAGGCACCGGAACAA[C/T]GTGCCCATTCGTGGA	154214
rs531005726	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125077907	AAGCATATGATACCT[A/G]ATCAGAACAAAGCTG	154214
rs531062504	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006913	GAGATCGCGCCATTG[C/T]GCTCTAGCCTGGGTG	154214
rs531064691	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030639	TCATATCCAGGTCAC[A/G]CTGATGCAAGAGGTG	154214
rs531070894	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071235	TGTGAAAGTAACATG[C/T]GTTTGGTAGAAACCA	154214
rs531106650	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017103	TCGTAGCTGTGAGTA[C/T]AACTTAAAATTTTTA	154214
rs531109692	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973669	AAAGTAATGGCAGAA[A/G]CCCCAATGACTTGCA	154214
rs531132039	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071621	ATTTCCATCTACTAC[A/G]ATGTGGACTTAATAT	154214
rs531196947	snp	A/C	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124985214	ACACTGTTTGTTCCC[A/C]GAAAAACTCCTGCAC	154214
rs531199912	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124974178	TGCCCAGATTCAAGG[A/G]GAAGGGACATTGACC	154214
rs531203484	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050993	AAAAAACATATAACA[A/C]TCAGCTATGATGCAA	154214
rs531226086	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125054968	GGTATGTGGTTGTGA[C/G]ATAGCATTTCATGTG	154214
rs531262737	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083915	ACATGCTTCACTCTA[C/T]AGATAGATCCTTCAC	154214
rs531296105	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968730	TGTGATTTTTCCCTC[C/T]TAGAGCTTTTATACC	154214
rs531323083	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125020607	TGATGTTAATTACTG[C/T]AGCTGGGCTGCCAAG	154214
rs531328036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045117	ACAATCCTTTATTGC[A/G]GTCATGAAATAAGTA	154214
rs531360922	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017713	TATTTAAATGCCATT[A/G]ACTTTGGAAGGTTAT	154214
rs531396778	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051997	AAGAGTCTGTAAATG[C/G]TGAAGGTGTTTCCAG	154214
rs531415660	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003679	ACCTATATTAAAATA[C/T]CACATTATACCTTAT	154214
rs531421373	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086978	ACTGTAATCATTTCC[A/C]GTCCCTGATGCCCCT	154214
rs531436097	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125072504	TACTAATAAGGAAAG[A/G]CTGTTAAAAGAGAAA	154214
rs531455372	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125037239	ATTTCTGGCAGAAAA[A/G]GTTTTACAACTTTAT	154214
rs531464084	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988970	TTCCAAGTTTTGCAG[A/C]TCTTTGAACAGGGGT	154214
rs531482381	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072639	AATTATATGTGAAAT[A/G]TGAGGCAAAACTTAT	154214
rs531541114	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073109	ATCTCCACTTTAAGA[A/T]CAAACACAATATATA	154214
rs531556455	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989432	AGTCATGGTAAGGTA[A/C]TATGCATGGCACTCC	154214
rs531644031	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025393	CTTTTGCTTTTATAG[C/T]GGGAGAAACTTGAGC	154214
rs531678886	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982494	TCATTGGTACCTCAC[A/G]TATGGGAAAATTCTG	154214
rs531693337	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125077500	CAACACATAGTAGCC[C/T]CATACACAACCCCTT	154214
rs531707400	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018142	TATGAGGGCTCCTTA[C/T]TTTCAAATTAGCATT	154214
rs531709528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012281	CACAACAGAATGACT[A/G]TGTTTCAGTTTGAAC	154214
rs531714826	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976190	TTAATTTTTACAAAT[C/G]TAAGCCTAGTCATTT	154214
rs531744678	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125053017	ACATTAGAACACTTG[C/T]TGTTTCCCCAATATA	154214
rs531770815	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019010	TCTGGGGAAAGTGTA[A/C]AGCCCCAAGGAAAAG	154214
rs531930377	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090231	TGTTACAGATTTTTA[A/G]TATGAAAATTGACAA	154214
rs531936184	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046157	GGGATGAGTAAGTGC[A/G]CGGCCCCCGAGGCTA	154214
rs531986652	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988654	CACCATCCATTTTAA[C/T]ACATTTTAGCAGATT	154214
rs531997025	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991389	AATATCAATTTCTCC[G/T]AGTGGCCTTCTTTTA	154214
rs532002385	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046854	TCATAGTTAATTTAT[G/T]TACTGTTTTTATGCA	154214
rs532019755	snp	A/G	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125074321	TAGATAGATAGATAG[A/G]TAGATAGATAGATAG	154214
rs532034425	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125023291	CAAATATGATTGAGG[A/C]ATAGCCTGCAATGGG	154214
rs532060161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026884	TAGAGTAGTATTATT[C/T]TCACATGCAAAGAGT	154214
rs532064596	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977095	TTGGAATCAGAATTT[C/T]CCATCCTACTTAAAA	154214
rs532118962	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968072	CAGGCATGAGCCACC[A/G]TGCCTGGCCCCATAA	154214
rs532181930	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125004941	GAGATTGATTTGGCT[C/T]ATGGTTCTGGAGGAT	154214
rs532206818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021497	GTCTTGAACTCCTGA[C/T]CTCGTGATCTACCCA	154214
rs532210453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013789	CAAGATTTTTAGTCT[A/G]GCAGATCTATTTCCA	154214
rs532245938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027355	ACTCTCTATGTCCGT[A/G]AGTTCAATTGATGTG	154214
rs532269603	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014322	AAATTCCAGGCTGTA[C/G]TCTAAATGCCTTGCA	154214
rs532303048	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006820	CGGGTGTGGTGGTGC[A/G]TGCCTGTAATCCCAA	154214
rs532312372	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970661	ATGGTATTTAAAGCT[A/T]TTAGACTGGATGAAG	154214
rs532405725	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125070507	TTCACACCAACATCT[A/G]TTGTTTTTTGACTTT	154214
rs532413682	snp	A/G	0.00119737	0.0244387	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963308	GTGTAGGGGATCCCT[A/G]TGTGCCCCTCATGGT	154214
rs532496282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007282	TGGAGTTTCCCTCTT[A/G]TTGCCCAGGCTGGTG	154214
rs532504136	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049988	TGGAAGTCATCAATA[C/T]TGGGGGCAGTGAAGG	154214
rs532513520	snp	A/C			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083029	TCTTGAAAAACACTG[A/C]GAGGAACCTTCTACC	154214
rs532531971	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048212	ATTCATGGCCACAGT[A/G]TGGCACCCTGTACTG	154214
rs532539684	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125038341	TGTTAACTTGATACT[-/A]AAAAAATTGACATTT	154214
rs532542082	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999336	TTCCTTAGCTGATTC[C/T]CCAGCAGATCCCTTC	154214
rs532550991	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125035106	TTTTGGGCAGAGACA[A/G]TGGGGTTTTCTAGAT	154214
rs532570441	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091008	TTGCAAAGGAAAAAT[G/T]ACGTTGAGATGAAAT	154214
rs532574442	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091020	AATTACGTTGAGATG[A/G]AATGTTGAGAAATAA	154214
rs532578326	in-del	-/TTGT	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125024177	AAAAGATGTAAATGA[-/TTGT]TTGAAGAATTAATAA	154214
rs532600020	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028603	GCAAAATGTATTATA[A/G]TTCAGTTTTAAAAAG	154214
rs532631347	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994041	TGGAGTGTGGAGAAG[A/G]GACTGGAAAGAGGGA	154214
rs532638792	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091823	GTGTCTGCTATTTAC[A/G]TGTTATTTGTTCCCA	154214
rs532664925	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077379	ATTATTAATAGGTAA[C/T]AGTTAATATAATAAG	154214
rs532682693	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124993217	AGATTCCTGAGGTCT[C/T]GCCCCAAGAAATTCT	154214
rs532682708	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125080827	CTTCCTTTTTCAATT[C/T]GTTAAAATGATTCAC	154214
rs532700250	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070629	TCATATGTTTGTTGA[A/C]TGTTGGTATCTCTTC	154214
rs532700262	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063749	GAAAGTTGTAAACAA[C/G]AGGTAATTACCACCA	154214
rs532703535	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124999871	AGCTATTAAACTATT[A/G]AATAAATATATGAAA	154214
rs532734522	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979606	GAGGCAATGAGGTTG[C/T]AGCAGCACAGAGAGC	154214
rs532746809	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076692	AGGATGTGACCATAT[C/G]ACCTGCTCACAATGT	154214
rs532765415	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022789	CAATCACACTTCCTT[C/T]CCTTTAATTTATGTC	154214
rs532786751	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125029514	TGGGTGGATGGTGCA[C/T]AAAGATACTTTGTTT	154214
rs532797013	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979001	GTCTTTGGAAAAAGC[A/G]CCATTTGATTGGCTA	154214
rs532820340	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125065084	ATCGAGATCATCCTG[A/G]CTAACACGGTGAAAC	154214
rs532828245	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965667	CCTCAGGGCTTTTGT[A/G]CTTGGTTTTCCCTGT	154214
rs532851259	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022134	GTGACCACCTACCTT[G/T]GCCTCCCAAAGTGCT	154214
rs532866977	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124966295	ACTTAACCTCTCTAT[C/G]CCTTAATTTCCTCAT	154214
rs532882561	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971951	TCATGGTTTCAAGTA[A/G]CACCTACCTGTTGTT	154214
rs532919420	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092902	AAGAAGCAAATAGTG[A/T]GGAAGTAAGAGATCA	154214
rs533001264	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057262	CTCGACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	154214
rs533038976	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086020	CAAGATTATTTTCAC[C/T]TCTCTATTACAAAGA	154214
rs533056860	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008526	CAGGCCTTGGTTTCC[A/G]ACTTCTTGGAGTGAT	154214
rs533058814	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125016549	TGGGACTGCTGTTTT[C/T]AGAAAGTTTTTAGAA	154214
rs533065739	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125049883	AAATGGAAAATTAGT[C/T]CAGTTTGAAATATGT	154214
rs533066693	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994675	GTATATATCCTCAAA[A/C]TACTACATCCTGAGC	154214
rs533076535	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124980944	AAATAGATATGTTCC[A/G]TGTGCATGTTGTCTG	154214
rs533109954	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001149	TTTATGAGGCTTTTC[G/T]TACAAGGGAAATAAA	154214
rs533141462	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042524	GAGCCTTGAGAAAGA[A/G]GGGAAGGTAAAAAAT	154214
rs533180678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078595	GAACCCACTCCCTTG[A/G]TAACTAACACGCTCC	154214
rs533197777	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124987083	TTCATAATTTGGACG[-/T]TTTTTATACGATTCT	154214
rs533204552	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125043062	CTCCTAAGATGGCTT[C/T]ATGCTCTGCCCTTGT	154214
rs533205405	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124983702	TTTTCTTACTGGCTC[A/T]GTAGGAAGAGGCTTG	154214
rs533217336	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030882	TCTCCGACCCCACAT[A/T]TTCCTCCCGCACTGC	154214
rs533270629	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036533	AAATGGGATCTAATT[A/G]AACTAAAGAGCTTCT	154214
rs533275990	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125024584	TTAGCCAGACATAGC[A/G]GTGCATGCCTGTAAT	154214
rs533285673	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995410	AGTTTCATTACAAAT[A/G]TATGCATCCCTAAAC	154214
rs533325417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030535	GCCAAAAGGCCAAAA[C/T]AAAGGGTTTAGAGCG	154214
rs533337094	in-del	-/TT			intron-variant	RNF217	GRCh38.p7	6:124980138	TTTTTTGTTTGTTTG[-/TT]TTTAATGTTTGGTTT	154214
rs533337374	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125016598	TCTTTTAAAGAAAAT[A/G]TGGCACATAAACACC	154214
rs533339005	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967063	AATCTTTAGCACCAC[A/G]GTATATGTTGATTTA	154214
rs533373600	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125012707	TGGGAGTTAAAGTTA[C/T]ATTTTACTTTTGTAA	154214
rs533423272	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125078400	GTGGCAGTGTGTTTC[C/T]GTCCATTCTTTATTT	154214
rs533473373	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052274	AATATAGCTTACCTT[A/G]TCATGCGTTTTGTGT	154214
rs533498951	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072576	GCCACATAAAGATTT[G/T]AGAACCCAATGAAGC	154214
rs533525056	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037394	CCTTTTTCTCTGGTT[G/T]CTTCTTGTTACTGTG	154214
rs533562748	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066350	ATGACCATAGAACCC[A/G]TCGCCCTCTGGACAT	154214
rs533644960	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125035206	CCTTCTCCTGCCTAA[C/T]TGCCCTGGCCAGAAC	154214
rs533646329	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031460	CAACACCCAAGTCAA[C/T]TCTTAAATGCTTTGC	154214
rs533677500	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974641	GTAGTTAAAATATTT[G/T]AAAAACTTAGGAATA	154214
rs533688144	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078974	ATGGAGTATAGGAAA[C/G]CCCTCCCACCCACTG	154214
rs533732483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988456	TGATTGTTAAATCCA[C/T]GAAAGCAAATGAATT	154214
rs533746025	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124995926	ACTCTTGTCTCAAAA[A/G]AGAAAAAGAATCAAG	154214
rs533747718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066511	TCTGTCTGGAATGTT[C/T]TTACCACAGATGTGT	154214
rs533749275	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125058789	CAGAAAACTTTGGAC[C/T]TGATGTCTATAGTAT	154214
rs533766548	snp	C/T	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125057428	CTCAAGTGATCTAGC[C/T]GCCTCAGCCTCCCAA	154214
rs533872635	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079808	CAAAAAATTAAGTAT[A/C]GGAATATTTAAATAA	154214
rs533891623	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125041637	CTGTCTCTTCCCCAT[C/G]TTCTCTGCATAACAG	154214
rs533919324	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125037510	GAATTTTTGGCTTGA[A/T]TTTTTAAATCATTTT	154214
rs533931172	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045615	GGCTGATGATAAGAG[A/G]GTGCTCTTAAGGAAT	154214
rs533938048	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125072669	TTAGAACAAGTTTTT[C/T]TGTCAGGAAAAGTGA	154214
rs533951708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997200	AAAATGTTCTGTGTG[A/G]TGATTGAAAGGATTT	154214
rs533952548	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125025454	CAGAGGGAGGTGAGA[C/T]TCCTGACAAGGCAGG	154214
rs533961596	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088053	AGACAGAGGTTCTCT[C/T]AATGTTGCCCAGGCT	154214
rs534019542	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089219	TGGATCAGAGGGCCT[A/G]ATAATAGTCTAAAAC	154214
rs534063637	in-del	-/CT	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088833	TGCTATATTCTGTCA[-/CT]CTATTCCATTATTAA	154214
rs534078974	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125080964	TTGGACCCAGGATGT[A/G]AATAAACCACTTCTT	154214
rs534085018	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089850	TTTTGTGAATGTATT[A/T]CTTCTTCAATATCCC	154214
rs534100438	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091590	TTAAAATTGAATTGT[A/T]CTTTAAAACCATAAA	154214
rs534130858	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990983	GAGGTGGGAAGATCA[C/T]ATGACCCCAGGATTT	154214
rs534145245	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081671	AAAGGTCAGAGGAGC[A/G]TGTTTCCTGTAGGAT	154214
rs534171626	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026538	TTTAGAGCATTGAGA[G/T]CGTAAACGTGTCATC	154214
rs534179037	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124990426	TGCAATTGATTTTAT[-/A]AGAGATATCTCAAAT	154214
rs534183692	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124980522	GCTTCCCCAGTTAAT[A/T]CCTATTTAATTACAC	154214
rs534188217	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053206	TCACTTGTCCCAGCT[C/T]CTATTCTGGCAGTTA	154214
rs534210671	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124983952	GCATGGCACCTTCTA[G/T]GCATCCTCACGTGAC	154214
rs534248929	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977219	TCAGGGAAAGTACAA[A/G]TGTACTAGCTGAATT	154214
rs534274535	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084578	TTGTTGGGCTCCAGA[A/G]TGTAAGAATATTTTA	154214
rs534299492	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997735	CTGCTCGCTCTCTCT[A/G]CAGCCCTGAACACTT	154214
rs534302414	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038986	TAATGCTCTCCCTCC[C/T]TCCACCCCATCCCCT	154214
rs534344226	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125013459	GAGACCTGAATGATG[C/G]AAGAAAATGAGTCAT	154214
rs534371563	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039454	GATTCATAAAACGAG[C/T]TCTTAGAGACCTACA	154214
rs534403855	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006252	ATGAACTTTTGACTC[A/G]AGTTTCCAAAATTCA	154214
rs534428870	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081907	AGTAAAAGATGCCAT[A/G]GGTACAAACAGATAA	154214
rs534460498	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963493	GAGGTCCTGCTCTCG[A/C]TCTGATCTCCCTGCT	154214
rs534491233	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074403	TTAAGTGACATTTTT[C/G]TGATTACTATGATTA	154214
rs534558030	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125068280	TAGTGCAGGGTGCTT[C/T]TCAATTAGTAGATAC	154214
rs534566714	snp	A/C	0.000108536	0.0073659	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048245	ACTAAGATCTTTGTT[A/C]TTTGTGATGAACAGG	154214
rs534602970	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999485	AAGCTTTAAAATTGT[A/G]GTTCAAACTCATTGT	154214
rs534603742	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091081	TTTTTAGAGCAATCA[A/G]CTTATTTCCAAATTA	154214
rs534619233	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034216	TGGAGCCCATTTGTC[A/C]ATTTTTTCTTTTGTT	154214
rs534627708	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041063	CTCTCTCACCACTCC[C/T]ATTAATGATCTTTGT	154214
rs534658656	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125009987	ACAGCTTAGCATTCT[-/T]TTTTTTTTTTTTTTA	154214
rs534668460	snp	A/G/T	1.82251e-05	0.00301864	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962903	GGGATCGAAAAGAGG[A/G/T]AGGGGATGAACAGCA	154214
rs534828729	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063286	TTATACGTTATAAAA[A/G]CAAATAAACAGTTAA	154214
rs534835184	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963709	CTTATACAGGATTGC[A/G]AGCACAAGCTTGCTC	154214
rs534845912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070393	GGATTGCTGGATCAA[A/G]TGATAGCTTTACTTT	154214
rs534867904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040496	GATGGATTCACTGCT[A/G]AATTCTACCAGAGGT	154214
rs534906622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063834	CAGAAAAAAAGTGAA[C/T]TGTATTTATTCATAA	154214
rs534915629	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991972	ACAGGTCATTAGTCC[A/G]TGACTGATATTGAAC	154214
rs534967588	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125013683	TGAATTCTGAGAAAA[G/T]GGATATATAATACCA	154214
rs534970954	snp	C/T	8.49798e-05	0.00651787	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082980	TGGTTGGAGTAGGAG[C/T]GATACCAAAGGGTAC	154214
rs534978175	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125054643	CTTAGGCAGCTTGCC[A/C]ACTAGTGGATACATG	154214
rs535021962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049572	GTCACCTTGAGTATC[A/G]TTTCCACGTCTTTAA	154214
rs535022144	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125057374	TTTCGTAGAGATGGG[A/G]TTTCACCATGTTGGC	154214
rs535031158	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076313	GATCATAGCATAAAC[A/G]AAATATACTTTCAAA	154214
rs535039853	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124985991	GAAACTCAGCCATCA[A/G]TGCAATAGTGTTAAG	154214
rs535044163	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125058198	GAATTATAACTGTCT[A/T]AATGCAGGTATGTGG	154214
rs535071508	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049927	TTTGAAGACCCTTTA[A/G]GGCATCAAAGAGATG	154214
rs535079282	snp	A/C/G			intron-variant	RNF217	GRCh38.p7	6:124971323	TTACATGTTTTGAGG[A/C/G]AGCGAAAGGCTGCCA	154214
rs535096047	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125069957	AGTGCACCCATTATC[C/T]GAGCAGTGTACACTG	154214
rs535099825	snp	A/C	0.000677579	0.0183938	intron-variant	RNF217	GRCh38.p7	6:125076875	TGAGTGTCTGACATA[A/C]TTATGGGTGTCTTCC	154214
rs535124161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021653	TATTCTACAAGGACT[C/T]ATATGAAAATGTTGA	154214
rs535135859	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092956	AGACCAAGGGGCCTA[A/T]ACAGGGGTGGGAAAG	154214
rs535155818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042651	GTGTTTGATTGGATG[C/T]TGGATGGTATCCCGA	154214
rs535172916	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124979115	CAGAGCTGGCAGTTT[C/T]GTTTTCAGGCTTCAG	154214
rs535188452	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085564	GAAATTCTAAAAACT[A/G]CTTTAAAAAGAAGCG	154214
rs535195505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994185	GTTTTATAAATGTTT[A/G]AACATATTTTTAAAA	154214
rs535227942	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086100	CATATCCATAAGGTT[C/G]TACATTTGTTTTTTA	154214
rs535282081	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078030	ATCTATGTGATCTCT[A/G]TAAAAATATTCTTCC	154214
rs535283922	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125047117	AGTTTTAGAAGGACT[C/T]GTAATTCCATAAATT	154214
rs535327607	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008084	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	154214
rs535393497	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092497	GATGAAAACTATAAC[A/G]GTTTTCAAACTATTT	154214
rs535394039	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000702	TGGCTGAAATACATG[A/G]GTATCTACATGCCTA	154214
rs535407573	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124973854	TATTTTGATGATGAC[A/G]TTGTGGGTCAGGAAT	154214
rs535423751	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065463	CAGGATATTCTAAGC[A/G]TTGCAGGACATACAT	154214
rs535458346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001287	CTTGTTACCAGTTTT[C/T]GTGTGTTTGTTCTCC	154214
rs535463276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966668	AATTGCATATTAAAT[A/G]TGAGTTGGACTATTG	154214
rs535517902	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125047224	GCAGTAATTAAAACA[-/T]GTACAAAATTGAATT	154214
rs535527573	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092141	CTGAAAATTAAGAGA[-/T]TTTTTTTTTTAAGCA	154214
rs535616420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036677	AAACATATTTACAAG[A/G]AAAAAAACATCAAAA	154214
rs535660938	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995962	AAAAACATTTGGAAT[A/G]TTTCTGGGTTTTTTT	154214
rs535662095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988204	GAACAGTTTCATCCC[A/G]AAACTATCACCCCTG	154214
rs535686316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030569	ATGCAAGTCCAAAAT[C/T]CAGTAGGGCAGTCCA	154214
rs535696716	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971705	GTGATCCTCCTGCCT[C/T]GGCCTCCCGAAGTGC	154214
rs535728484	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041798	CCCCATGTTTCCCTC[C/T]CCTCTTATCTTTCCA	154214
rs535734475	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037480	TTTATCTTGCTTAGA[C/G]TCAAGAGATTTCTGG	154214
rs535739968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003774	CAATGTGATTTTTTT[A/G]TTGTCTTTATCTATT	154214
rs535742751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996921	AGTATAAAAATGATC[C/T]GTATTTTCTTTAAAT	154214
rs535753149	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024167	ATTGGAGATCAAAAG[A/T]TGTAAATGATTGTTT	154214
rs535803964	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981661	ATGACTTTCTGTCCT[A/G]GACTTGTGAAGATAC	154214
rs535852848	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058285	TTTTATAAACCATGT[A/G]TATTCTTATTTTTGC	154214
rs535915109	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967211	AATATGGCTAAAGTA[C/T]GTAGTCCCAGGGATG	154214
rs535925255	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050530	AAATATTTTCTCATG[C/T]GGTAAAAGAATTTTC	154214
rs535935557	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010847	AATGATCTAAGGTCT[G/T]CCAGCTCCAAAGTCC	154214
rs535973891	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018385	TTTGGCTTTAGTTTT[A/G]CAACAGAATGATCTC	154214
rs535990758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051333	AATCGTCTCTCTCTG[A/G]TGGCCCCCGAGATCG	154214
rs536025481	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071335	AGCTGGCAGTCACCC[A/G]TGCCATCACGAGGGT	154214
rs536038700	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124974747	TATCTAATGACACTG[A/C]AGAATTAACCATCCT	154214
rs536088023	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021429	TGCCACCATGCCCGA[C/T]TAATTTTTTGTATTT	154214
rs536118639	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125008656	AGGTCAGGTCAAGAT[A/T]TCCTTGTGACTGTAT	154214
rs536136036	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125043571	ATTTAATCATTTTTT[A/C]ATGTTTAAGTTATAA	154214
rs536148031	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079253	GGCAGATTATTAAAG[A/G]AATGGTACTGGGAAT	154214
rs536175978	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125029463	TTCTTTATTGAATCT[A/G]AAAACTCCAGGTAAT	154214
rs536179612	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989801	ACTCTGTCCTATATT[A/G]TTGATTTTTCTCTTT	154214
rs536243306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047099	TAAGATCAGGAAATT[A/G]CTAGTTTTAGAAGGA	154214
rs536249695	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039064	GTCCATGTGTTCTTG[C/T]TGTTCAACTCCCACT	154214
rs536265223	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982128	TTTTTTATTTTTGTA[A/G]CTATCTTATTTAGGA	154214
rs536278201	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997379	AAGATATTCCTGGAA[A/G]TCATTCCTACCCTAG	154214
rs536309322	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975781	GTGGGAAAAGTGACT[G/T]TGATTCTCTTGCCAG	154214
rs536397545	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082364	AATGTGCAGGACAGA[C/T]AGAATTATAAAGTAT	154214
rs536402068	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124968350	GTGTGTGTGTGTGTG[C/T]GTGCGTGTGTGTCTG	154214
rs536403047	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125074424	ACTATGATTAATGGC[C/T]GTTATTAGTTCACAA	154214
rs536464774	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984785	ATATTTCTTAGAACC[G/T]GAGAAATACAACTCT	154214
rs536465333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075276	GTGAAGTAGTAGACT[A/G]TTTTTAGGAGGTCTC	154214
rs536477320	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124986698	AAGGCCAGACAGTAC[A/G]TATTTTAGGTTTTGT	154214
rs536543503	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125005071	GGGGGCAGAACTCCC[A/G]GGATAACAGCATTAA	154214
rs536596612	snp	A/C	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124987731	TCCTCCTGCCTCAAC[A/C]CGTGGAATAGCTGGG	154214
rs536597920	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124970784	CAGAAAGAAGAAGCA[A/G]AGAGTCTAAAAGGGA	154214
rs536605451	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125005959	AGCCTTGAGGAATAG[A/G]TCAGAAAAGGTGTTT	154214
rs536617541	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997870	TTAATTTTTTCATCC[C/T]GTAGTATCCCTTTGA	154214
rs536647033	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063212	GTCTGAGTTAAGAAG[A/G]AAAGTTTCTAAGTCA	154214
rs536654519	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998452	TCCCAAAATTCAGAA[C/T]TTCTCTACCATTTTT	154214
rs536675007	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124991649	AGGTGATCAACAGAC[A/G]TTTGTTTTAAATAGT	154214
rs536677555	in-del	-/CCC	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124993255	AATTCTGGGATGTGT[-/CCC]CCCAGGAATCTGTAT	154214
rs536677749	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089926	ATAAATATCTAAATT[A/C]TTTCATTTTATAGAA	154214
rs536713839	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039556	CAAGACAAAATTAAC[A/G]AGGACATTGAGGACT	154214
rs536718052	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124994836	GCCTGAATTTTATAG[C/T]TCCGTGGCTGACTGT	154214
rs536718548	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087250	AAAGTTAGTGGCCTC[A/T]ATAACCTTAATTGGC	154214
rs536721602	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964237	TTGCACAATCCTGGA[A/T]GCCCTTTGATCCTGT	154214
rs536742074	snp	C/G	0	0	intron-variant	RNF217	GRCh38.p7	6:125007351	CCTGGGTTCAAGCGA[C/G]TCTCCTGCCTCAGCC	154214
rs536745526	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991118	AATGTCTCCTCAGAG[A/T]AAAGGCCAAAGATCT	154214
rs536776660	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033076	GTCTTTTGTGAAGTA[A/C]CCATAAAGTCTCGAC	154214
rs536801063	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125048428	AAAAAAAGGTTGCTG[A/C]TAATGTCTGACGTTT	154214
rs536807360	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999682	TAAAATGATGAAAAC[C/T]GCTTTGAAAAGCTTG	154214
rs536871964	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993937	TTAATCTATGACAAG[A/G]AATTGAGGCCTTTAT	154214
rs536875554	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092100	AAGAATCTTCCTGCC[A/G]ACAGGTAGGTCCTGC	154214
rs536877895	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124987083	TTCATAATTTGGACG[A/T]TTTTTATACGATTCT	154214
rs536892538	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027590	CTTCGAAATCTTAGC[G/T]GTTGTAAACAGAGCT	154214
rs536896193	in-del	-/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125044310	CATGAATATAAAGAG[-/T]TATTGTTCACTACTT	154214
rs536898390	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966825	CAAAGGCCAATTGGT[A/G]GGTGTCATCAATATT	154214
rs536911240	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990431	TTGATTTTATAAGAG[A/G/T]TATCTCAAATTTGAC	154214
rs536931839	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068927	GTAGGATGACATGTA[G/T]AATCACAGAGAGGAG	154214
rs536934870	in-del	-/T	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125027958	TCAAATCATTGCCCA[-/T]TTTTTTAATCAGATT	154214
rs536950766	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125064842	GTGTATGTACGTGTG[-/TA]TATATATATATAGTT	154214
rs536973933	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028924	GTGAATTATTTCAAT[C/G]AAACTTCATATTTGA	154214
rs536977824	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:124987019	AACATCTTTTCACAC[A/G]TACAGGTTTTGCCGA	154214
rs536993119	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062779	ACGAGGTTTCACCAC[A/G]TTGACCAGCTTATCT	154214
rs537037516	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963627	AATTTAACTTTGCTG[C/T]GAACTTCAGGCTATG	154214
rs537047363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055089	TCAAAATGAATGAGG[C/T]ATCTTCAGAACAAAA	154214
rs537062878	snp	A/G	0.0103295	0.0711199	intron-variant	RNF217	GRCh38.p7	6:124984556	CAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA	154214
rs537074591	snp	C/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966885	ACTTAAATACCTCTA[C/T]GCTCTGTATAAAATT	154214
rs537080572	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006917	TCGCGCCATTGCGCT[A/C]TAGCCTGGGTGACAA	154214
rs537091821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022346	CAGTGAAATTATAGG[C/T]AGTAACAGTTTTGAA	154214
rs537115917	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047751	TTAGTAGAGGAAAAG[A/G]AAATTTGCTTTGGTG	154214
rs537210269	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091092	ATCAACTTATTTCCA[A/T]ATTATTATTTCATGC	154214
rs537245654	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041086	ATCTTTGTTCTGACT[A/T]CTGTTGAAAATGAGC	154214
rs537303099	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041850	CCCATAAAAACCACA[C/T]TTCACTGAAATCTAA	154214
rs537319460	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125050022	TTGTCATTGAACTTA[C/T]GAAAATGAAAAAAAT	154214
rs537381005	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050366	TATACAATGGCACTT[G/T]TGATGCATCTTTCAC	154214
rs537395897	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077044	AGGACACTACTTATA[A/T]GAGCAAGTAGTAATT	154214
rs537441360	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970335	CTAGAGTGATACAGG[A/C/T]GAACGCAGTTTGAAC	154214
rs537444290	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125043482	GACATGTTCCTGCAA[A/G]GCTTCAGTACCTAGC	154214
rs537467069	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086264	GGTAATTTCCTTTCT[G/T]CCTGATTAGCCAAAT	154214
rs537495575	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052736	TGCTGTACCTCTCCA[C/T]ATCTCATCTTCAAGA	154214
rs537500086	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036718	GGATATGAACAGACA[C/T]TTCTCAAAAGAAAAC	154214
rs537506163	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124978752	CTCATTTGTTCTCAC[-/T]GCCCACAGCTTGGCA	154214
rs537512672	snp	G/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962210	AGACCCCTCTGTCCC[G/T]CCTGGGGCTCGCTGG	154214
rs537528417	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125078121	AATGATTTTCCAGTG[C/T]GTGCCGCTTCTTAAT	154214
rs537559607	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015612	CACTATTTTACTTAC[A/G]TTTTAATATATATAC	154214
rs537563282	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125030748	GCATTGAGTGTCTGC[A/G]GCTTTTCCAGGCACA	154214
rs537594039	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056892	AATAAAGGAAGTCAG[A/G]TAAAATATCCTCCAT	154214
rs537624401	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008159	TACTTGGGAGGCTGA[A/G]GCAGGAGAATGGCGT	154214
rs537643242	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028075	TCTCCCATTCTGTGG[A/G]TTGTCTCTTCACTTT	154214
rs537656471	snp	A/G	0.00597247	0.0543191	intron-variant	RNF217	GRCh38.p7	6:125065541	ACTAAATTCTGAAGC[A/G]TCTCCTGGGGCATGA	154214
rs537669952	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017161	TTTGAAAACTTTTTA[C/T]GACACTGCCTTTCAA	154214
rs537678261	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125026952	TATTAATGTTTATTA[A/T]ATTTGTTGAATGAAC	154214
rs537686040	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125037078	CAGCACAATTTATTG[-/A]AAAAAAAAAAAAGTC	154214
rs537699944	snp	A/G	0.000798403	0.0199641	intron-variant, missense, synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:124966750	AGATGTCAACTTGGA[A/G]GATAGGAATATGGAT	154214
rs537730109	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125021035	AGTTTGGCAATATGT[G/T]TTAAAAGTCTCACAA	154214
rs537738008	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125093080	TTTGTTGACCAAAGG[G/T]TAAGTACAAGAATTT	154214
rs537793856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058734	CCAAGCAAACAGCCA[A/G]GGAAGACTCTCCTAC	154214
rs537796123	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967375	TTCAGAAATCTTCCA[A/C]CAATATTTTTCTTTT	154214
rs537809514	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994257	CACAACAATTAGTGA[C/T]TTATGAACTATTTTG	154214
rs537812366	snp	C/T	3.30901e-05	0.00406743	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045348	ACTTGGCCGTATTGA[C/T]TCCAGCACCAAGCCA	154214
rs537845315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994920	GTTGAGGTATACTAC[A/G]AGAATTTTTTATGAT	154214
rs537858965	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051721	ATTCCCATTTCCTTA[A/T]GTACACTTAACACAG	154214
rs537885453	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125019181	GATTTCATGACACCT[C/T]CACGAGGAGGTTGTA	154214
rs537887553	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125003515	TCCAAAGATGATTGT[A/G]GGAATAAACTTTAGA	154214
rs537904839	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014508	AAACAGTGTATATGC[C/T]TTTCTGATGCAGGAA	154214
rs537921915	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960825	TCTGTCTTTAAAACA[A/G]TAAGCACTTAAAGTA	154214
rs537933066	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988284	AAAAAGGTTGGGGAC[C/T]ACTGCATTAAATGGT	154214
rs537977261	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074269	CCAAGAAACTCTCCA[A/G]TTAGGTAGGTCGGTA	154214
rs538015984	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088030	TTTTTTTTTTTTTTT[C/T]TTTTTTGAGACAGAG	154214
rs538016854	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997040	AGGTTCTACAAACAC[A/G]GACGTGCTGGTAGAG	154214
rs538026572	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024303	GGAACATGAAGGAGG[C/T]CAGGCACGGTGGCTC	154214
rs538027517	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030965	GGCATCCGGGCGTTT[C/T]CCTACATCTTCTGAA	154214
rs538059061	snp	A/G	0.0142736	0.0832652	intron-variant	RNF217	GRCh38.p7	6:125074885	ATTGTAAAACTCCCA[A/G]TTGCTTTAAAACATT	154214
rs538074944	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125079991	TTTATTTCCTATCTC[A/G]TTCCTTCAATTCTGT	154214
rs538087879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016876	CCATGGCACGCGTAT[A/G]CCTATCCAACAATCC	154214
rs538088009	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024657	CCCGGGAGGCAGAGG[A/T]CGCAGTGAGCCAAGA	154214
rs538097651	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974571	AACACTTAATATTAT[G/T]CTGTATAGCATAATT	154214
rs538114895	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031661	CACCTCAGCCTGGAC[A/C]TTCTTGTTCATATCA	154214
rs538139380	snp	A/G			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963824	CTGGTGGAGAAAAGA[A/G]TTGGAATAAATATTT	154214
rs538145291	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017594	GAGAAGTGTTCACAT[G/T]TCTCTGCACTTGATA	154214
rs538186520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975919	TTTTCCACCTCAAGA[C/T]TTTTAAAAAATATTT	154214
rs538270684	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011712	AATTTTTTTAAAAAT[C/G]ATTTACTAGGAACCC	154214
rs538296243	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019563	TTTTAGCTTTCTATA[C/G]TAATTACAAATTAAT	154214
rs538325211	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125060840	ACCCAGAATTCTGCC[A/G]CCCCAGTGTACTTAC	154214
rs538325794	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125071817	TGTCATTCATGATTT[A/G]TGAGTGGCCAGTTTT	154214
rs538333803	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125004085	TTCTTTAAAATTCAT[C/G]CATCAAATAAGGTTG	154214
rs538452514	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017983	TTTTGGTTACATCCA[A/G]TCTTCTAGTAGCACA	154214
rs538521323	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072848	CTACTTAGCATAATA[A/G]AGAAACACATGGATT	154214
rs538550101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032209	ACCATATCAGCTGCT[C/T]TCTCCACTACACAGT	154214
rs538558311	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983005	AGAAGCACATATAGG[C/T]GTCACAGTAAAAGGA	154214
rs538563583	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039711	AAGTAAAACACTCCT[C/T]AGCAAATGCAAAAGA	154214
rs538585543	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073578	GCAACCCATAGCAAG[A/G]AACATGAGTTTTGCT	154214
rs538613179	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081758	ATTATTAACCCTTTT[A/G]TAACACAAAGCTAAT	154214
rs538614848	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125026395	TCAATGGAAAATGCT[C/T]AGAATAGTGCCTGGC	154214
rs538621617	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124998940	GCCCTGAAAAAGTAC[A/G]TGTGGAATTGACTCC	154214
rs538634491	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033146	CATATAATTAATACA[G/T]TTCAGAGTTTGGATT	154214
rs538689467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969382	TTTTCAAATTCAGTT[C/T]GTCAGAAGGGTTTTA	154214
rs538690969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024321	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	154214
rs538697914	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985865	TATTAATAAAGGGGT[A/G]TTGTGAACATGGTTA	154214
rs538778121	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962059	GGGCCCTGCGGCTGG[C/T]CAGCGCTCCGGCTGC	154214
rs538786598	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047839	CGGTGGGTGTGGGGT[A/G]GAAATCTCATTACAC	154214
rs538813282	snp	A/G	5.43483e-05	0.0052126	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962866	CTGCAGTTGGAGCTG[A/G]AGGAGGAAGAGGAGG	154214
rs538820653	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125054206	AGAAATAGGGAAGAC[A/G]TCTTGAAGAAAGGAG	154214
rs538821432	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125063188	TTATACCACAGATTA[C/G]ATACTAAAGTCTGAG	154214
rs538821479	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027578	ACACTTAGGTTGCTT[C/G/T]GAAATCTTAGCTGTT	154214
rs538854202	snp	A/G	0.0162398	0.0886349	intron-variant	RNF217	GRCh38.p7	6:125010404	AGTGACTTGATGTAA[A/G]AAGTTATAATAAGAT	154214
rs538870019	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125015071	TCTGAAGTATATAGA[C/G]TTCCACCTAACACTT	154214
rs538900633	snp	A/G	0.00593009	0.0541284	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082981	GGTTGGAGTAGGAGC[A/G]ATACCAAAGGGTACA	154214
rs538902220	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998501	TATTGGTCATAACAT[G/T]TAAAAACTGTGTAGA	154214
rs538914433	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971631	CAGCTAATTTTTGTA[A/T]TTTTAGTAGAGATGG	154214
rs538918748	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063245	AATTAAAAGTGAGAT[G/T]CATGCTAAAAATAAC	154214
rs538929808	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090048	ATTTTTTTAAGTGTC[A/T]TATGGCAACTCCTCA	154214
rs538978431	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125050433	AGAAACTCTGTCTGT[G/T]TGCTTACCTTATCTC	154214
rs538984800	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964362	TTATATACTTTCACA[G/T]TATCTTATATTATCT	154214
rs538996527	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090558	GTTCTAAGGAATTAT[C/T]GTCATCCTCTAAGTA	154214
rs538998761	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991243	CCATTGCTCACTCAG[A/G]ACCAGCTTCTCGGAC	154214
rs539035607	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124984120	AGAAGCAAACATTCA[C/T]ACCACAGCAATAAGT	154214
rs539057561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056495	AAGTACTTTTACTTC[A/G]TAGTTGCACAAGAGG	154214
rs539080450	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091407	GGTCCCTCTATTTAA[A/G]GTGCTAAGGAGAAAG	154214
rs539081455	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125034141	TTTCTCCCATTTTGT[A/G]GGTTGCCTATTCATT	154214
rs539107521	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061502	ATGTGGGACAGATTG[A/G]GGCATATTTTTATTA	154214
rs539114296	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045762	AGGCTTTTTCTTTAT[C/T]ATTATGGACTTGATT	154214
rs539145313	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027668	CTTTTGGGTATATAC[C/T]CAGCAGTGGGATTGC	154214
rs539153642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978179	GCTCTCCAGGCAAAT[A/G]TGGGGCCATGTATAT	154214
rs539158899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000537	TGAAAACAACTACTG[A/G]TTCATCCTTAAATAT	154214
rs539191022	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125075509	GGGGAAATGCCAGAC[A/G]CTTACAAAACTATCA	154214
rs539204299	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084100	ATCTCTTGCCTCCTC[C/G]TCTCTGTTTTTATTT	154214
rs539221359	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021231	ATTATACAATGTTCA[G/T]AAACAATGATTATAG	154214
rs539251298	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124987057	TATTAGTCTACTAGC[A/G]TGTATGCACATTCAT	154214
rs539267670	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085035	ATATATGTCATATGT[A/G]TGATATATATGAAAT	154214
rs539288339	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125014081	CAGGGCTAGTGTGTA[C/T]ACACATACAGAGGAT	154214
rs539339620	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077512	GCCTCATACACAACC[C/T]CTTCCCACACTGGTA	154214
rs539351499	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125055728	TCTGACTTAATGTTA[A/G]ATGCATAAGGAAAAG	154214
rs539374799	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124979740	GACAGTTTGCTTGAG[C/G]TGTAACATGACAATT	154214
rs539383838	snp	C/T	0.0244538	0.107838	intron-variant	RNF217	GRCh38.p7	6:125033825	AACTGTGTAAAAGTG[C/T]TCCTATTTCTCCACA	154214
rs539394207	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007428	TTTTTTGTATTTTGA[A/G]TGGAGACAGGTTTTC	154214
rs539400630	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125070948	GGAGACAAATACTTG[C/T]GGGCAGATGTATACT	154214
rs539404787	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125065540	AACTAAATTCTGAAG[C/T]GTCTCCTGGGGCATG	154214
rs539474968	snp	A/G			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006472	TTACAATTATTCCAC[A/G]GAAATTTACAGCATG	154214
rs539474983	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016201	TATGGTTCTTTCATT[A/C]TTCTTTGTACTTTTC	154214
rs539475303	snp	G/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125008047	GGATCACGAGGTCAG[G/T]AGATCAAGACCATCC	154214
rs539493187	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041268	TTGTTACCTCTCAGT[C/T]ATCTATCATCTACTG	154214
rs539505034	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965988	ACTGAATTTTTGAAA[A/G]GCCTGAGATTGCCCC	154214
rs539528972	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091293	ATGGTGCTTTGTGTG[A/G]TGAGTATATAACATT	154214
rs539535086	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008993	CCCTGGTTTAATGGT[G/T]GAAAATGATATATTA	154214
rs539547818	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062594	GTTTTTGTTTTTTTT[A/G]AGATGGAGTCTCACT	154214
rs539555899	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016830	AGGTAATACCTAATA[C/T]AGATGATGGGTTGAT	154214
rs539559048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041975	TGATTATAAAAAACT[C/T]GGCTTTCGAGAAAAT	154214
rs539622527	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125035415	ACATTCTTAAAGAAA[A/G]GAATTTTCAACCCAG	154214
rs539656137	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975325	TGTTTAGAGTTTAGC[A/G]TATTATTAATTTATG	154214
rs539669117	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978104	AAACAATGTGTCCCT[A/G]TAGAATAGTCCATGG	154214
rs539705823	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125010318	TCTCATTTATTAGTG[A/T]TCAAATATGTTCAAT	154214
rs539706503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070547	GCCATTCTTGTAGGA[A/G]TAAGGTGGTATCTCA	154214
rs539747178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972381	CCAGTGATGCTCTCT[C/T]GGCTCTCTCCAACTT	154214
rs539796417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071137	AGGAGGACAGGTACT[A/G]TTTTCTTCATGCAGA	154214
rs539869542	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973452	TATTACCTTGGTTCT[A/C]CCCCATTATTCTTTG	154214
rs539878130	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973735	GCTAGCATCCCATCT[A/G]TCACTGAGGTGTGTC	154214
rs539911443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065355	GTAAAATAGAGTTTG[A/G]TTCTAACTTAAGATA	154214
rs539943457	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124966297	TTAACCTCTCTATGC[C/G]TTAATTTCCTCATCA	154214
rs539960452	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966553	AGAGTTATTAGTGAC[G/T]TTTTTCCACCATTTC	154214
rs539972993	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058214	AATGCAGGTATGTGG[A/G]AAAAGAGTATTGCTC	154214
rs539988491	snp	A/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125058408	TAGGAAAAATATAGC[A/G]TAAAAGTGATATAAA	154214
rs540080283	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051191	TTAGCCTACACTTCA[C/T]CTAAAAAAACAAACT	154214
rs540081453	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125002727	TTTTCGTGCTGGCTT[A/C]TCAAACTTCATATCC	154214
rs540095824	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001240	TATGTGAAATTCTAT[A/G]TAAGTTTTCTTGTAT	154214
rs540117397	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044046	GCAATGTTAAAAGTT[A/T]CTATGAATTTAGTTT	154214
rs540124525	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003129	ACACACACACACACA[C/T]ACCTATTCACCTTCA	154214
rs540134081	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086389	ACTTTTGGATTGCCT[C/T]ATTTTAAAACTTGAG	154214
rs540142600	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125044386	AATCATTTAAAAATT[A/G]GTTGTGTCCACACTT	154214
rs540205903	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988850	TTGACTCCTCAAATA[A/G]ACAATAACAGTTAAG	154214
rs540242752	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989384	TCTTTCTTCTTTTGA[C/T]GTATGCAATAGTAAT	154214
rs540258205	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125079445	TACTCAATTAAAAAA[A/T]AAAAAAAAGACAAGC	154214
rs540305260	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125039383	GGTAAAGGGATCAAC[A/G]CAACAAGAAGAGCTA	154214
rs540314443	snp	G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125036371	TTGCTATTGTGAATA[G/T]TGCTGCAATAAACAT	154214
rs540332053	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009346	CTTGTAATCTCTTCA[A/G]AACACCTCCTGTGAA	154214
rs540350995	snp	A/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966877	AGATGGTGACTTAAA[A/T]ACCTCTATGCTCTGT	154214
rs540362144	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982372	TTTCCTCAAAAGTAC[A/C]AACTTTACTGAAAAA	154214
rs540370751	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989919	CCCCCTTGTAGGGCT[A/C]CATTTTTCCTTGCAG	154214
rs540388936	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025301	CATTAAATAATCTTT[A/C]ATTTGGCTTGGCTGC	154214
rs540394124	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125010144	TCATGTAACTGAAAT[C/G]AACGTTTTCTTACAT	154214
rs540421208	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091721	AGTAACTGTATGGTA[C/T]TTCAGGAATTTGACC	154214
rs540460349	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011166	TTTTTCTTCTTTTAA[A/C]GTTTTGTCTAAGGCT	154214
rs540472987	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125064113	TCCTGCAATTCCTTA[C/G]TACTTCATATATCAC	154214
rs540485459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051862	CCAGGACTTTGGGCT[A/G]TGCAAATCAGGGAAG	154214
rs540492078	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967912	GCCTCCTGAGTAGCT[A/G]GGATTACAGGTGCAT	154214
rs540517401	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125056129	CCATCTTTGACTACT[A/G]CATTTTAAGTTGTCA	154214
rs540542402	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124971454	ACTGTTAAGTTTTTT[-/G]TTTGTTTGTTTGTTT	154214
rs540546813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044709	AACAATTTTTAAACT[A/G]TTAGGCATTATACAT	154214
rs540547408	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067658	GAGCCATGAAATGAT[G/T]ATGAGTTTGGTTTTG	154214
rs540552230	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060289	TTATCACATATTTTC[A/G]TATAAATGCTTTCAA	154214
rs540560469	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037093	AAAAAAAAAAAAAGT[C/G]CTGCCCACTGCCCTG	154214
rs540591379	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012833	TTTCTTATTTATATG[A/C]TTATGTTTTGATCAC	154214
rs540594873	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124996188	ACAGTACTTCATCGT[A/G]TATTTAAGTGTTTTG	154214
rs540616565	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124969506	TCAACTTTATCACTA[C/T]TATTTGCCCCACCAA	154214
rs540652886	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962113	GCGCCACAGGCCCCT[C/T]GACCCTTTGACCACC	154214
rs540662639	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125012100	TTTGATATGTAGTCT[C/T]GCAAAAGAAAAAGAT	154214
rs540681546	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045915	CTAAATTTGGGGGCT[A/G]TAGAGCAAATGTGAT	154214
rs540681846	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038261	ACACGGAGCAGCAAA[A/T]TATCTTTAAGTACAT	154214
rs540707083	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125079271	TGGTACTGGGAATAA[A/T]AGTGGCTGAGGATAA	154214
rs540736824	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090259	CAATTTTGTTGCTTT[C/T]AGAAGCAATTAACAT	154214
rs540741040	in-del	-/GGG	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125068044	TTATATTTTGCAGAT[-/GGG]GGGGGTCATGGATAA	154214
rs540744655	snp	A/C	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125031782	CTGTTCCAACCTCTG[A/C]CTGTTACCTAGTTCC	154214
rs540788513	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049161	GCTTATCAATATAGA[G/T]AACAAGTTAATGATG	154214
rs540841698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998541	GCCGTGGCTCAAACC[C/T]GTAGTCGCAACACTT	154214
rs540878808	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991274	TCTTTGCTCTTTCTC[A/T]CATCAAACCCATGTC	154214
rs540904111	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125060083	TTATGTTTTGCCCCA[C/T]GGAACATTTCTATTA	154214
rs540950414	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125000504	TAATATTCTATAAAG[-/A]AAAAAATTATTATTT	154214
rs540965523	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125061120	TGTGTATTATAAATA[A/G]TGTGTTGATGATATT	154214
rs540973603	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961312	AGTAATACTTCCTGT[A/T]AAATAAAGATAGATC	154214
rs540975945	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052852	CCGAATCTGACAGCC[A/G]TGATTTTTACATGTT	154214
rs541003873	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027826	TATTTGTTATTGCCT[C/G]TCTTTTGGATACAAG	154214
rs541006780	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125018005	AGTAGCACATAATCA[A/G]TTGACTTAAAGTTTT	154214
rs541040884	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053602	TCTGGGGTTTTCTTT[A/T]GTTTTAGACACTGTT	154214
rs541042666	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125062488	AATTAATTTATAGAA[C/T]ATTTTTATGAAAACA	154214
rs541070487	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982625	TTTATAGATCATTTA[C/T]TAATAATATATTTAC	154214
rs541079092	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125069239	GGCCTTAAAAAGCTA[A/G]CATTATAGCAAGAGA	154214
rs541084571	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125046647	AAAGGCTGTTTGGAG[C/T]CATCTCCATTTAAGG	154214
rs541123977	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971218	ATTTCATTTATAAGG[A/T]AAACTTATATTTTTC	154214
rs541133136	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089513	ATAATCTAAAGTAGG[C/T]CACATTGAATGTAAC	154214
rs541139312	in-del	-/CCCTTCCTTACA/TA	0.300421	0.244863	intron-variant	RNF217	GRCh38.p7	6:124976300	CTTTCCTCCCTTCCT[-/CCCTTCCTTACA/TA]CCCTGTCACCTGGGC	154214
rs541167148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055455	TTGCTATAATTGTCT[C/T]CATTAGAGATTCACA	154214
rs541194561	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090071	ACTCCTCAATAGCTT[A/C]CTTTTATTATTTGAT	154214
rs541308164	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074640	AACCTTTTCATTTCT[C/T]CTTTCACAGAACTCT	154214
rs541322522	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124985711	TGTGTATAGTATAGT[-/A]AAAAAAAACATAAAT	154214
rs541362431	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091571	ACACCAGAAATTAAA[A/G]CCATTAAAATTGAAT	154214
rs541455532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076578	GAAACTGGTAAGTGT[C/T]GTTTCATAAAATTTG	154214
rs541499479	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124998238	TTTGCCCCTCTATTC[G/T]CCTATCCCATGGATT	154214
rs541562142	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979381	AGTGAGCAAGCATGT[A/G]GAAATAGGGTGTGCA	154214
rs541574548	in-del	-/TTAT	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125021143	GTTATTCATCCCACA[-/TTAT]TTATAATAGCATTAA	154214
rs541581510	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125033091	CCCATAAAGTCTCGA[-/C]TATTTTTCTTTTTTT	154214
rs541611804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070554	TTGTAGGAGTAAGGT[A/G]GTATCTCATTGTGTT	154214
rs541625514	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047956	TGTAGAAGAGAAGAT[C/T]GATAACAGAAGAAGT	154214
rs541638771	snp	G/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125022524	CAATTAGCACATTGA[G/T]TGCAACAGCTGAACT	154214
rs541681786	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124997867	CTTTTAATTTTTTCA[C/T]CCTGTAGTATCCCTT	154214
rs541686054	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040857	AAACTACATGATTAT[C/G]TCAATAGATGCAGAA	154214
rs541690745	snp	A/C	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124999205	ATCTTTGGTATATTT[A/C]ATTTTAAATTTCCTC	154214
rs541715647	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965413	ACCCCGTCTCTACTA[A/C]AAATACAAAATTAGC	154214
rs541726480	snp	A/G	0	0	intron-variant	RNF217	GRCh38.p7	6:125008411	AGAAAGAAGTTAAGC[A/G]TTAACCAATCCTGGA	154214
rs541751862	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995720	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	154214
rs541844134	snp	C/T	0.0566069	0.158427	intron-variant	RNF217	GRCh38.p7	6:125035015	TCTGTTATTGGTGTA[C/T]AAGAATGCTTGTGAT	154214
rs541903219	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124979079	GTGATAGAAGTTCTC[A/C]CTCTGGTCATTGACT	154214
rs541904646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987093	GGACGTTTTTTATAC[A/G]ATTCTTTAGATTCAT	154214
rs541930453	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042891	ACTGACCTCAGAGTA[A/C]AAAATTCAGGCTCTT	154214
rs541931096	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125021960	GATCTCAGCTCACTG[C/T]AACTTCTGCCTCCCA	154214
rs541940598	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994405	TTGAACGGAGACATA[A/T]TTACACCTAAATAAT	154214
rs541972995	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125057218	TCTCTCTCTGTCGCC[C/T]ATGCTGGAGTGCAGT	154214
rs542138553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024447	AATTAGCCAGGCATG[A/G]TGGTGCACGCCTGTA	154214
rs542150243	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966082	ACTTAAGACAAAAGA[C/G]AAAGGGCTTAAAGCG	154214
rs542158107	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125060905	CCCTATTTAAATGGC[-/T]TTTTAAAAAGTTTTA	154214
rs542185044	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057692	TGGGAGATTTTCTTA[A/C]AGCTAAATTGGTTTC	154214
rs542193273	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125049776	GAGTAAAAAAGAATA[C/T]AGTTGAAAGAAAACA	154214
rs542212675	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065826	ATTTAGCTGTTGGCT[C/T]AGTCGGTAGGCAAAT	154214
rs542243344	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125017072	CTTTGCTTCTTTTCC[C/T]TTTTGCTGCAGTAAA	154214
rs542282307	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966938	AGTTCTTCTCCAGTT[A/G]TTGCCATGACTGTGG	154214
rs542302773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010292	ATTTACCATGTTTTT[A/G]TCTATTTTATTCTCA	154214
rs542344338	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085765	GTATGTGTCCTTCCA[A/G]ACACTTTCTACAAAT	154214
rs542418720	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988685	CTACTTGAGATTGTA[C/T]TGAATTTGTGTTTTC	154214
rs542422208	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045081	TGATTAACATTCATT[A/T]TGTTATCTTAAAAAT	154214
rs542442004	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968234	GTCCTGAAAATGTGA[A/G]GAATAATATGAGACT	154214
rs542450706	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124980115	ATATTTTACCCATCT[C/T]GAAGGGATTTTTTGT	154214
rs542485978	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045687	AATCTAGTAACCTTA[C/T]AGGAAGGCTGATCTT	154214
rs542491056	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087403	ATATTTGTGGCTGAA[A/G]TCTCTCCCAACTATT	154214
rs542527513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037743	GCTTGTAGTAGATCT[A/G]TGTATATTTTGTGAT	154214
rs542534455	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980971	TCTGTATTTTAGAAG[A/C]ACATAAACTCTGTAC	154214
rs542537710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989421	AGTAATGCAAGAGTC[A/G]TGGTAAGGTAATATG	154214
rs542562774	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125015611	TCACTATTTTACTTA[C/T]GTTTTAATATATATA	154214
rs542572636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974129	CTAAGTTTGGAAGGC[C/T]CTCAGCATAACTTTG	154214
rs542579133	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125080326	TTTTTAAATTAGATA[C/T]TTAAAACAGTGTTGT	154214
rs542600133	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072360	TAAAATACTCAAATT[A/C]ATCTATAGAGCCATA	154214
rs542623917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066264	TGCTGTTAAACATAA[C/T]GCAGATTACATCACT	154214
rs542641560	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073049	TGGTAGATCACCCAC[A/G]ACACTGCTATCAGTG	154214
rs542662837	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052158	AAAGCTAGTATTGAG[A/G]TGAATGCATTGTGCA	154214
rs542663675	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974754	TGACACTGCAGAATT[A/C]ACCATCCTGGTCAAT	154214
rs542685234	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125058888	CCTTATGTGGTTCCT[A/G]CCCTTTGCCAAATTT	154214
rs542692254	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125072129	CATAAGAAATGTATT[A/T]TCCCCTGGTAGTACG	154214
rs542716305	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032512	ATTTTGTCAAGTAAA[G/T]AAAGCTAGGTGAATA	154214
rs542745899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976692	GTGCTTTTTCTAGAG[A/G]TGGGGTTTCACCATG	154214
rs542755759	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125070865	TGGGGGCAGTAATAC[A/G]TAACAGTCAACTTAG	154214
rs542757057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992068	CTTGTTAACATTGCA[A/G]ATTCTGATTTACTAA	154214
rs542874115	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125004186	AAAACAGGGCTTGCC[A/G]GTTATATTTCCCCTT	154214
rs542886527	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996563	ATTGCAATCTGAATT[C/T]TGTCCCCACAGCTCT	154214
rs542909973	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088301	AAATGTTACCTTTTG[C/G]ATGCAAACCAATGAT	154214
rs542922539	snp	A/G/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125029872	CGACAGCACTGTGTA[A/G/T]GGTGGGATTCCCATA	154214
rs542925129	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997271	GGCTGCTTCACTACT[C/T]GCATGTTCCCCACCC	154214
rs542944456	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038351	GATACTAAAAAATTG[A/G]CATTTTTGTAGATAT	154214
rs543000431	snp	A/C/G	0.00200543	0.0316026	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962975	TGGGGGCCGCCGACG[A/C/G]ACTGGTCCTGGACGT	154214
rs543002532	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047109	AAATTACTAGTTTTA[A/G]AAGGACTCGTAATTC	154214
rs543016087	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982465	CTTGGATATTTTCTA[C/T]AGCAAAAATGTGGTC	154214
rs543020790	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006393	GTTTAATCTCACTTT[C/G]CTAGCATAGTTACTA	154214
rs543056543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998610	CAAGACCATCCTGGC[C/T]AACATGATGAAACCC	154214
rs543095108	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991319	TCCAGTAGCTGTTCA[C/T]CTTTCCCATAATATT	154214
rs543100923	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025889	TATTCTGTCAAGTAC[A/C]AGGTGAAGTTTTTGA	154214
rs543163399	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018937	ACTCCATTTGGCCAC[A/G]TGTTCCAGCACTAAC	154214
rs543167931	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125076165	TTGCAAATACATTTA[C/T]ATCTGCTATAATTTC	154214
rs543186350	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040552	TGAAACTATTCCAAA[C/T]AATTGAAAAGGAGGG	154214
rs543211938	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027335	CCTCTAGTAACCATC[C/T]TTCTACTCTCTATGT	154214
rs543223626	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125061348	TAAGTATTTTTTAAA[C/T]ATTAATTTAATAATT	154214
rs543224804	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125019834	CCCCTTTTTTGCAGT[G/T]GGGGGGGAGTGAAAA	154214
rs543247605	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125034277	TCTTTGCCCATGCCT[A/G]TGTCCTGAATGGTAA	154214
rs543252258	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013003	ATTTCCAGAAAGTTA[A/G]CATTTCTATCTTGAT	154214
rs543264664	snp	C/G	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962341	ACGAGGAGGAGCGGC[C/G]GGCCGGGCCAGGCTC	154214
rs543283295	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125020348	AAAGAGGGCTTGAGA[C/T]AAATCAATATCTGTT	154214
rs543294839	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053732	AGCACAGATTTCTGG[C/T]AAAACTAAGGGTATT	154214
rs543310390	in-del	-/A			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967689	TACTGTAGTCACCCT[-/A]GAGTCAGTGACCCAG	154214
rs543312269	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999049	CTTGCAGTTGATTTA[C/T]AGCAGTATTTGACAT	154214
rs543325045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053717	CTTTCATCTCAGTAT[A/G]GCACAGATTTCTGGT	154214
rs543328951	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125044383	TTTAATCATTTAAAA[A/C]TTAGTTGTGTCCACA	154214
rs543337885	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021368	ACCTCCCGGATTCAA[C/G]CAATTCTCTGCCTCA	154214
rs543343543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978278	CCTCTGCCTGGACCT[C/T]GCTCAGGGACTTCTG	154214
rs543352031	in-del	-/TGTA	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125017747	TACATATTAACTGAC[-/TGTA]TTTTTTTATTGTGGG	154214
rs543439484	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090174	ATAGAATAATAATTA[C/G]TTTGTATATATATAA	154214
rs543443438	in-del	-/A	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125001490	TAAAGACGTAATGAT[-/A]TGTTTTGTCAACTAG	154214
rs543474122	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125039982	AGAGCACTAAATGCC[C/T]ACATCAGAAAGCTGG	154214
rs543536795	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125033325	CATTAGGTATATCTC[C/T]TAATGCTATCCCTCC	154214
rs543554623	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125048812	TTACCTGTCCATTTG[C/T]CCTTCCAGGCCCAAC	154214
rs543583849	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125051322	AACAAGTGAAGAATC[A/G]TCTCTCTCTGATGGC	154214
rs543678677	snp	G/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125042246	TAGCTGTTCCAAACT[G/T]CCAATTACTGGCTTG	154214
rs543692301	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092574	TTTACCACATGATGT[G/T]TGCAATACATCATGC	154214
rs543724363	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069335	CTGTTTCTTATTCAT[G/T]TGGAGTTTTACACCT	154214
rs543744029	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062928	CCATTTTTTATCTTA[A/G]CAATGAGTTTTCTAT	154214
rs543757857	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084442	AAGCCTAAAGCTTTA[A/T]ATTGTCTCCAAATTC	154214
rs543763077	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077326	AGTTCCATTATGTCT[A/C]TATAAGTGATAAGTT	154214
rs543766963	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124971324	TACATGTTTTGAGGA[A/C]GCGAAAGGCTGCCAC	154214
rs543793039	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125069995	TACATTATGCCTCAT[C/G]CCTTTCCCACTCTTA	154214
rs543837838	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124995690	ACTTTGGGAGGTCGA[A/G]GTGGGTGGATCACCT	154214
rs543862829	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125080960	TTCTTTGGACCCAGG[A/T]TGTAAATAAACCACT	154214
rs543888404	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071108	ATTTTATTGAATTAA[A/G]TGTAAACAACTTGAG	154214
rs544003097	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999939	ACAAATTGACAAGAT[C/T]AGTTTAATGAACAAT	154214
rs544064326	snp	A/T	0.0126979	0.078662	intron-variant	RNF217	GRCh38.p7	6:125035099	AAGGAGATTTTGGGC[A/T]GAGACAATGGGGTTT	154214
rs544066743	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995515	CTTTTACTTTATTCA[A/G]AGTTAACATTTTGAG	154214
rs544068324	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124976608	TCTTCATAGTGATTC[C/T]CTTGCCTCAGCCTCC	154214
rs544068901	in-del	-/AGTA	0.00438332	0.0466095	intron-variant	RNF217	GRCh38.p7	6:125048651	GCTATTTTATAGCTG[-/AGTA]AGTGCTTCTCACATG	154214
rs544072598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986633	AAAAGAATTTTATAA[A/G]GTTATCTCTTCCCTG	154214
rs544105310	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125034945	TTCCTAAATATTTTA[-/T]TCTCTTTGAAGCAAT	154214
rs544108955	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993694	GCTGGGCGGCACATA[G/T]GAAGGCCGGGTAGGC	154214
rs544117709	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124972791	TTGACCCCCTATATC[A/T]AGATTAAGCATCCTT	154214
rs544215926	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125077744	ATTCCTTTTCTGGCC[A/G]TGTTTCTCATGTGTA	154214
rs544279666	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125064504	AAATCAATATGTTGT[C/T]TTAGTTATAAAATAG	154214
rs544286094	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979957	GCCTTTAAAAAGTGT[C/T]GGAAGTGCATTGTCT	154214
rs544288941	in-del	-/CAC			intron-variant	RNF217	GRCh38.p7	6:125041902	CAGTATTCGGTTATG[-/CAC]CACCAAGAAAGTAAA	154214
rs544296211	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124976486	TGTTGGCCAGGCTGC[C/T]CTCAAACTCCTGACC	154214
rs544332609	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125015377	TATAAGTTTTTCTAC[A/G]AAAATAATCAGAAAT	154214
rs544345914	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125015877	GATTAATAAAATATG[A/G]TATATTCATAGGATA	154214
rs544347905	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023401	GAAGTATTTTAATTA[A/G]TGGAGTTGTATGATC	154214
rs544352931	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125065276	AGCCTTGGCAGCAGA[C/G]TGAGACTCTGTCTCA	154214
rs544377060	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024493	GAGGCTGAGGCAGGC[A/G]GATCACCTGAGCTCA	154214
rs544395721	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030867	GGACACTGTGTAGGG[A/T]CTCCGACCCCACATT	154214
rs544456674	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125008271	AAAAAAAAAAAAAGT[G/T]ATGTGAATGTGGTCT	154214
rs544480068	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974191	GGGGAAGGGACATTG[A/G]CCTCAACTTATTTTG	154214
rs544505362	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009973	AATGTGAATTGAAGA[C/G]AGCTTAGCATTCTTT	154214
rs544526860	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125017922	ACTTTATAAAAGAGG[A/G]TACCACATATTTTCA	154214
rs544625255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059089	GAGCATAATAATAAT[A/G]AATGTACAGATTTAC	154214
rs544630056	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982841	GTGAAAGTAATTTAC[C/T]CACTTCCTGGTGAGA	154214
rs544655227	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125011990	TCTTTAAAATCAAAA[A/G]CCACTTTCTACTTTT	154214
rs544682448	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125052105	TTCTCAAGTTCAGAC[A/G]TGCTGTCCAAGAAAA	154214
rs544693012	snp	G/T	0.0337553	0.125452	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087217	CTTTTATACTGGCTG[G/T]TACATTAGAATTACA	154214
rs544732917	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045823	TCTTGTTCTGTCTAT[A/G]ATAGGTAAAAATAGT	154214
rs544779456	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085364	TATTTTTAAATTAAC[A/G]TACACATTTTTCTCT	154214
rs544796636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046491	CACCCCAGAACAATT[A/G]TCTTCCAAATTTTTG	154214
rs544796663	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038448	AATGAAATGACATGA[C/T]ATCTGGTATTTTCTT	154214
rs544904758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066327	ACAGAGCAAAAGTTA[A/G]TTCTATGATGACCAT	154214
rs544911327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080438	GGCTGTATTAGTTTC[C/T]TTTTTAGTGTAATTG	154214
rs544929951	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125031940	TAATTGGACTTACAG[C/T]TCCGCATGTCTGGGG	154214
rs544952400	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982505	TCACGTATGGGAAAA[C/T]TCTGTAGTCTAATCC	154214
rs545036901	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124968474	TTTCCTTGTTCTTTT[A/T]CTTTTTGAAATCTGA	154214
rs545068684	in-del	-/CAGT			intron-variant	RNF217	GRCh38.p7	6:124987190	AGCTCCTCAGTTGCA[-/CAGT]CAAATGGATTTTTTA	154214
rs545073872	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961207	TGTGTAAATTGAATT[C/T]CCTCTCAGGAGAAAA	154214
rs545079655	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994192	AAATGTTTAAACATA[A/T]TTTTAAAATATAGGC	154214
rs545084785	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068520	ATATATTTGTTAGTA[C/T]AATTGATTACTCTCT	154214
rs545112821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027184	TTAAGTTATTTTAAA[A/G]TACACAATTAAGTTA	154214
rs545128331	snp	G/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962565	CGAGGAGCAGAGCAC[G/T]GTGAGCGGCGGCGGC	154214
rs545139952	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997419	AATTACTTAACCATA[C/T]GCGAAAGTGACTGTA	154214
rs545159877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977598	TGGCTTATTACAATC[C/T]AAATGGATTTGACAG	154214
rs545167404	snp	C/T	0.00557542	0.0525036	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971663	GTTTCACCATGTTGG[C/T]CAGGATGGTCTTGAT	154214
rs545175255	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033818	TCCCACCAACTGTGT[A/G]AAAGTGTTCCTATTT	154214
rs545215774	snp	A/G	5.63206e-05	0.00530633	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963021	CCCGTCCCTCGCCAA[A/G]AGACAAGTCTTCTGC	154214
rs545255527	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089325	GTGGACATTCATCCA[A/T]CCTGACCCCAGGTCA	154214
rs545287015	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125081420	TCCTTAAATAATTTT[G/T]CCTTTTGTTTTCCAG	154214
rs545305363	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125032627	TTTCTGGAAGGAAAC[A/G]ACAACCATTTTGTGG	154214
rs545331267	snp	A/C/G			intron-variant	RNF217	GRCh38.p7	6:125008553	TGATTCTTTCTCCAC[A/C/G]CAGTCAAGCTGATGA	154214
rs545335054	snp	A/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:125059383	CATTAAAGAACAACT[A/T]GAAAATGAGGCCTTC	154214
rs545363900	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090794	AAAAGAGATTTCATT[G/T]ATTCTTTTTAATGAT	154214
rs545367833	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991423	ACCCATGTATACATG[C/T]TACCAACCCTCATCC	154214
rs545384694	snp	C/T	0.000798403	0.0199641	intron-variant, splice-donor-variant	RNF217	GRCh38.p7	6:124983523	TTATATAATTAAAGG[C/T]AGATACTAAATACTG	154214
rs545387155	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976742	ACTCCTGGCCTCAAG[A/T]GATCCACCTGCCTGG	154214
rs545406040	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047824	AGTTAAGATCCTCAG[C/T]GGTGGGTGTGGGGTG	154214
rs545429778	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125004147	TAAAAGGAAATATTA[G/T]ACAAATGTTAAATTA	154214
rs545432601	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124992310	AGGTGAAACCTTAAA[A/T]ACTGGTTTTGTACAA	154214
rs545458315	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125057642	TTGGGGCCTTGTGAG[A/C]CTTCAGGTTCAATCT	154214
rs545473065	in-del	-/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125019545	ATTTTCCCCTTTTTA[-/T]TTTTTTAGCTTTCTA	154214
rs545559757	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986425	TGTCCTTTGGGTTTT[C/T]ACAAAGATACTCTAA	154214
rs545593549	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054608	ATGAGCACCCATGCT[A/G]CACAAAGCTCATGCC	154214
rs545609785	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006482	TCCACAGAAATTTAC[A/G]GCATGCTTTTTTAAA	154214
rs545639354	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076452	TTGAGTACCTGAAAT[A/G]TTATCAAGCTTTGCA	154214
rs545639630	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125027521	AATAGTACTCCATTG[G/T]GTATATGTACCACAT	154214
rs545671260	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124998670	GTGAAGCATGGTGGC[A/G]TGCACCTGTAGTCCC	154214
rs545692692	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125015253	CTCTATTACTTTACA[A/C]CCCTGTAAAATATAT	154214
rs545695515	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125070171	CATCCAAGTTTCTGC[A/C]AAAGACATTATTTCA	154214
rs545702019	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125042632	TACTGCAGTAGAAAA[G/T]AAGGTGTTTGATTGG	154214
rs545757950	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007809	TACATTCCAAGACTC[C/G]CAGTGGATACCTAAA	154214
rs545771856	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971742	TACAGGCGTGAGCCA[C/T]GGCACCCGGCCGATT	154214
rs545807595	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040650	AAAGAGGAAAACTAC[A/G]GGACAATAACCCTCA	154214
rs545818164	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008324	TACTCTCCTATTTTG[A/G]GACCATAGTTGACCA	154214
rs545873271	snp	A/C			downstream-variant-500B	RNF217	GRCh38.p7	6:125092724	GCCTACAGTTACTGG[A/C]GTAATTTCTACATTG	154214
rs545873740	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029831	ACATAAAAGGAACAT[C/T]GCTATCTGTGAATTA	154214
rs545888384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056989	GAAATATGAAGGCCC[A/G]TTTCTGACGGTTTTC	154214
rs545902113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028199	TGCCAGATATAGTTT[A/G]TTAGTTTATCTTAAT	154214
rs545920355	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125042300	GGTCTTGAGTGGGCC[A/G]TGAAACTGGAATGCT	154214
rs545932116	snp	G/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125034995	ATGATTTGGCTCTCT[G/T]TTTGTCTGTTATTGG	154214
rs545948247	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978316	TCCACCTGCTTAGCC[C/T]GGCAGGCTGCATTCC	154214
rs545954998	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125021500	TTGAACTCCTGACCT[C/T]GTGATCTACCCACCT	154214
rs545970072	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000906	TTTTATTCTTTCTTT[G/T]ATATGTAATGCCATG	154214
rs545983364	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971420	ATTTGGCTTAGGAAA[A/G]CTATGATTTGATTTG	154214
rs546028974	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090133	GTATTTTAAAAAGTA[A/G]ACCAACCTTATGTTT	154214
rs546041231	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000387	TGAGAAACACACATA[A/G]TGTTATATGATATGT	154214
rs546098987	snp	C/T	1.97334e-05	0.00314107	intron-variant	RNF217	GRCh38.p7	6:125082847	CCTAACTAACTTTAA[C/T]TTTTTCTTATCCCTA	154214
rs546107102	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063551	TGTCAGTCTCCTCTG[G/T]AGTTACTATAAATAT	154214
rs546126852	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056157	TCAATTGTCAAAGAA[A/C]AAATGCCGTTTAGTA	154214
rs546170903	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077830	TTGCTTTATGAAAAT[A/C]TTTATATCTCTCCTT	154214
rs546206152	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000195	AAAACCTTGCCACAT[A/C]GTACCATTATTTTGA	154214
rs546226808	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087455	CTGCTTTATTGTTTT[C/G]TGTTAATATCTATTA	154214
rs546237431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965302	TTATTGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	154214
rs546292254	in-del	-/TGTT	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124969222	AATATTTCTCAGCTA[-/TGTT]TGATTGCTGGAAATA	154214
rs546302640	snp	C/T	0.0023933	0.0345097	downstream-variant-500B	RNF217	GRCh38.p7	6:125092920	AAGTAAGAGATCAGC[C/T]TAGGGTGGTCTTTAC	154214
rs546323321	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	RNF217	GRCh38.p7	6:125092648	ATTCTTGTCTTTTTT[C/T]CCAATAGGTTTGGAT	154214
rs546363964	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085044	ATATGTATGATATAT[A/G]TGAAATATTCCCATA	154214
rs546367376	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042803	GAGTGGCTGTGAAAT[G/T]GCTGCTTCCATTGCT	154214
rs546386592	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084657	CAGCATGCTTTCATT[A/C]TTTCTGAATAACACA	154214
rs546405966	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077394	CAGTTAATATAATAA[C/G]TATCAAATGCCCTCA	154214
rs546407998	in-del	-/AAGTC	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:124965878	TACACTTAAGTAATT[-/AAGTC]AAGACAGAAGTTTTC	154214
rs546426169	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042557	TCAATGCAGAGAGTA[C/T]GAAAGCAAGAGGAAG	154214
rs546431626	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987333	TTTGAAACTTTTTTT[A/G]TTCCCCCTAAGAGAA	154214
rs546436441	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994163	AGGGATGTGTGTGTA[A/T]CTTTTTGTTTTATAA	154214
rs546517647	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124979611	AATGAGGTTGCAGCA[C/G]CACAGAGAGCAGAGG	154214
rs546563843	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980287	GCTTCTCAATAGTTT[G/T]CAATTTGCTTTTTTT	154214
rs546595482	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997160	TTCTGTTTTGACCAG[A/G]CATAGAAAAGAGAAT	154214
rs546596347	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965700	CAGGAAGGTTCCCTC[C/T]ATGGCCCTCTTATCT	154214
rs546597379	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008048	GATCACGAGGTCAGT[A/G]GATCAAGACCATCCC	154214
rs546599356	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015956	GCATAAGTAGATCTT[A/T]AAAAATGTGTGAAGA	154214
rs546660537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008530	CCTTGGTTTCCAACT[C/T]CTTGGAGTGATTCTT	154214
rs546669099	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023912	GAATGTTGGTTACCA[C/G]GGGATGGGCATGGGG	154214
rs546712824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050219	CATATCGATTTGGAG[A/G]AAGAGTTGAAGGTCA	154214
rs546738984	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001828	ATGCTGAGTGGAATG[A/C]TTCAAAGCAAAGATA	154214
rs546773323	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966619	CATTTAAGAAAATAA[A/G]AGAGTCCCTATTAAA	154214
rs546775110	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125043163	TGCTGTTCATCTTTA[A/G]GAGCCGTCCCAAGGC	154214
rs546831242	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011664	TTTTATATGAGAGAG[C/T]AAGGAGTGTCAGGTT	154214
rs546833175	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125003157	TCAGAGTTGTAAGGG[A/G]GGCTAAAAATCAGAT	154214
rs546884964	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125047342	AGTGAAATGTTTTAC[A/G]TCTCATTTCATCTGA	154214
rs546906120	in-del	-/AAAT	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085588	AGAAGCGTGCACATA[-/AAAT]AAATATCTTTCTATC	154214
rs546944007	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030541	AGGCCAAAACAAAGG[A/G]TTTAGAGCGCCCATG	154214
rs547010308	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068648	TTTGTTTATACAGTT[C/G]GTTAATGTCTGTATA	154214
rs547026153	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024608	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC	154214
rs547044635	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065394	AGAGTTTTACCAATA[A/T]GAATGTCCGATGCAT	154214
rs547062849	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031488	TGCTGCTTAGAAATT[G/T]TTTTCATCAGATACT	154214
rs547070386	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124974312	AATTTTAATTTTTTT[A/T]AAAAATTTTGTCTTT	154214
rs547093285	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124974386	GTAAATAACTTTGGT[G/T]GTGTGTTTTTTGTGC	154214
rs547104928	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967129	TCATATTATATTGCT[C/T]GTGTACATAAATCTG	154214
rs547105729	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065898	ATAGCTACTCAACAT[C/G]TTCAACCGGATCTAA	154214
rs547149670	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038592	CAACCTTCACATATA[C/T]TTTAATTATCCCTAA	154214
rs547159748	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124990131	ATACTTTCTTCACTT[A/G]ACTTCAAGGACACCA	154214
rs547168797	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058646	CCACTTTTCATCTTT[C/G]TTTTGATAATCATGC	154214
rs547184702	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990448	ATCTCAAATTTGACA[C/T]CTCAAAAACTCAGTT	154214
rs547209373	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025461	AGGTGAGATTCCTGA[C/T]AAGGCAGGTGGAAAT	154214
rs547228450	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059231	TGGCTTTCTAATAGA[A/C]GTGATGTCTAAAGAT	154214
rs547261289	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125071255	GGTAGAAACCATATT[G/T]CAAATTTTGAATTTC	154214
rs547280956	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060525	TCTCGGCTCACTGCA[A/G]CCTTCGCCTCCCAGG	154214
rs547318868	snp	C/T	1.75419e-05	0.00296152	intron-variant	RNF217	GRCh38.p7	6:125045181	AACCAGTGACGTTTT[C/T]TTCCTTCCATCTGCT	154214
rs547328852	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996773	TACCAAATACTACAA[A/G]TATTGCAGTTTTAAA	154214
rs547340193	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125061595	ATTTTCCCTGTTTTC[G/T]ATTTCTTCCTTTTTA	154214
rs547392639	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019946	GCTTAGTCAGCTTTG[C/T]GGAGAAGAGCCCAGT	154214
rs547416347	snp	C/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124989736	AGGTCGTAGGCTGTA[C/G]CAAACAGGCAGCAGG	154214
rs547494536	snp	G/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962740	TGCGCGGACACCAGC[G/T]CCCCAGAGCCCGCGA	154214
rs547496309	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982075	CACAAGGAATTTCCT[C/T]GTGGGCAAATTGTGA	154214
rs547536116	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073322	ACATGAACAACAGAG[G/T]GTAAGTGCTGGACTA	154214
rs547562233	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081713	AATTTTTCAGTCTAT[A/G]AACACTGTGATTCAT	154214
rs547583707	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982607	ACTTATAATCATTGC[C/T]GTTTTATAGATCATT	154214
rs547598827	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125067274	GGACTTTGCAAACAA[C/T]ATTAAGATAGTTGGG	154214
rs547623466	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047442	AAAATTGACAAATAG[A/G]AGATTCTATATTTGT	154214
rs547624720	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082328	GATTTTCGTATGTCA[A/C/G]CTTGGGTTTAGCAAG	154214
rs547628111	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019430	TTTGTTAATTAATAA[A/T]CTACATTTAGAATAC	154214
rs547653021	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090362	TTAACAAAGAACCAG[C/T]TGTTTTGATTCTATT	154214
rs547669218	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984762	CTGTATAACCTTAGT[A/G]TGGAAAAATATTTCT	154214
rs547669778	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124969187	CAAAGTTATAAATCT[A/G]TTACTTATTTCTTAA	154214
rs547685852	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082803	TAAACATAGACATTT[G/T]AAAATAGGAAAACCT	154214
rs547686509	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125040222	AAGAAGAAAATAGAG[A/G]AGAATCAAATAGACA	154214
rs547706116	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961901	ACACCCACTCAGGGT[A/G]TGCGTGTGTGTGTGC	154214
rs547713292	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976811	TATCTGGCCTCAGGT[A/G/T]TAGCTTAAATCAACC	154214
rs547733907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012526	ATGATTATAATTTAA[C/T]GTGAACCTCATTGAT	154214
rs547754576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978071	GCTTAGCACCATGCT[A/G]ATCATTATGATAAAG	154214
rs547773387	in-del	-/TAAG	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007033	TGTTACAGTAATTAT[-/TAAG]TATGTAAATAAAGTT	154214
rs547790290	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978357	CAGACCAGATCCTGT[A/G]CCCACCGTGGCTCTG	154214
rs547792077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013227	GAGAAGAAACAGGTA[A/G]TAAACAAATATACAT	154214
rs547855701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047032	TTTATTTCATGCTAT[A/G]TATCCTTAGATTATT	154214
rs547879547	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:124971479	TTGTTTGTTTTGAGA[C/T]GGAGTCTCACTCTGT	154214
rs547885078	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125080865	ACTTTCAACGTACTA[G/T]GTATTTATTCATAGT	154214
rs547917430	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006601	TAACAACCTAATAGT[C/T]TCCTATCAGTGGACA	154214
rs547963768	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125007322	GCGATCTCGGCTCAC[C/T]GCAACCTCTGCCTCC	154214
rs547968370	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998783	AACCTGGGCAACAGA[A/G]CGAGACTCTGTCTCA	154214
rs547970615	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063120	AATCTAAATTTTGTT[A/G]GAGGTATCAGAATAT	154214
rs547994166	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124993701	GGCACATAGGAAGGC[C/T]GGGTAGGCCAGCTGT	154214
rs548002246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014473	TGTTATCATTAAGTT[A/G]TTTGGTACAGCTATT	154214
rs548011799	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999550	ACTTTAGGCTCATAG[A/G]CTGTAGTTCTGCCAG	154214
rs548022471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033039	AATACATTTTCATAT[A/G]CTCACTGGCCATTTG	154214
rs548026075	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125007899	AAGTGTAATTTATAA[A/G]TCAGGCAGAATAAGA	154214
rs548046201	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077962	GTAAAAGATAGAACA[A/T]GTATACGCAAATGCA	154214
rs548056102	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125045128	TTGCGGTCATGAAAT[A/C]AGTAATACTGTATAC	154214
rs548068316	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125021456	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATCTT	154214
rs548084509	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033462	TGGTTTTTTGTCCTT[G/T]TGATAGTTTACTGAG	154214
rs548085436	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000334	TAAAACAAGACTCTT[C/T]TACTATAGTGATAGT	154214
rs548091313	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047469	TTGTGTAATTTTGAG[C/T]GAGCCCATGGTATTC	154214
rs548107256	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124992091	TTACTAAGCCTGAGA[-/T]TGGGGCCTATACTTT	154214
rs548118511	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125075272	CGTAGTGAAGTAGTA[C/G]ACTATTTTTAGGAGG	154214
rs548137962	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985707	AGAAATGTGTATAGT[A/G]TAGTAAAAAAAACAT	154214
rs548227061	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125013943	GAAACATAATGCCCC[A/G]CTGACTACATGTGCA	154214
rs548242667	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124996097	GCTTGGTATTGCCAA[A/C]TTGTTTTCCAAAGTG	154214
rs548244377	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993383	CTTCTCCTCCCCTCC[C/T]GTCCTTTCCACTAAA	154214
rs548245363	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029669	TGTTGTTGGTAAAAA[G/T]GTAGAACGTGCATTT	154214
rs548251793	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124973761	GTGTCTTCTTTAATT[A/T]CAATACCTGTTCTGG	154214
rs548298983	snp	A/G	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:125035258	GAGTGGTGAGAGAGG[A/G]CATCCCTGTCTTGTG	154214
rs548349314	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015342	TTTTAAAAGTTCGTA[C/G]TTGTAAAGTCAGCAC	154214
rs548355743	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125000827	TGTAGTAAAAAGATT[C/T]CTTTAAAAATAAAAT	154214
rs548358766	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055596	TAAATATAATCTAAG[A/T]CTGATTAAAAACTAG	154214
rs548411878	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005232	AGGTTTATAACTACT[A/G]TGGAAAGGACTGATG	154214
rs548434631	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125008240	CAGCCTGGGTGACAG[A/T]ATAAGACTCTGTCTC	154214
rs548438805	snp	A/T			missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076826	TCCCAGAGAGACCTC[A/T]TTTAAGGAGATTAGT	154214
rs548448976	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041064	TCTCTCACCACTCCT[A/G]TTAATGATCTTTGTT	154214
rs548466034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057400	TTGGCCAGGCTGGGC[C/T]TTAACTCCTGACCTC	154214
rs548525558	snp	A/G/T	1.65729e-05	0.00287857	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058073	CGAAATTGAGCATGG[A/G/T]CAGAGGAATGCCCAG	154214
rs548597906	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965870	CTCTGTCTTACACTT[A/G]AGTAATTAAGTCAAG	154214
rs548603868	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125081123	GAAAATGGAAAGGAT[-/C]TTAAGGAAAAGCACA	154214
rs548608858	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124993876	AATTGCAGTGGCTCA[A/G]TAGAAGCAGGAGATC	154214
rs548657818	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125070420	CTTTTAGTTCTTCAA[A/G]GAATCTGTTTTCCAT	154214
rs548677071	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125053782	GTAAGGTTCTTTTAT[A/C]TTTTGTGAGTTCTGG	154214
rs548705424	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077422	TCAGTGCATACAAAC[A/C]CAAGTTTAATTATCC	154214
rs548770173	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979699	TGGAAATTATACTTT[A/G]TTTCAACTATGATGG	154214
rs548791678	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125071223	ACTTTTCCATGATGT[A/G]AAAGTAACATGCGTT	154214
rs548809311	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972858	TCAAACTATATAGGA[A/C]TCTTCTATACAATTA	154214
rs548816493	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086219	ATTGTACAGGAGTGC[A/G]TAATTTTTAAAGAAA	154214
rs548835494	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125008516	AGCACAGTCCAGGCC[-/T]TTGGTTTCCAACTTC	154214
rs548851285	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036684	TTTACAAGAAAAAAA[A/C]CATCAAAAAGTGGAT	154214
rs548856961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065164	GACGTAGTGGCAGTC[A/G]CTTGTAGTCCCAGCT	154214
rs548857621	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988221	AACTATCACCCCTGA[C/G]CCCCATCCATGGAAG	154214
rs548894756	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973596	AAAAAGTAAGGTAAC[A/T]ATTTGAATCGGAACT	154214
rs548899706	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966357	AACCCACCAGTTCCA[A/G]AGCAAAACAAAGTCA	154214
rs548932220	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974392	AACTTTGGTGGTGTG[G/T]TTTTTGTGCTTTATC	154214
rs548968831	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975417	CCATCTTTTTGAAAG[G/T]AATTAATTAATGAAT	154214
rs549045736	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125002100	TTTGGTATTGTTAGA[C/G]AGTAAAATACTGGAG	154214
rs549065175	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065995	AGTAAATGGCCACTC[C/G]AGTCTTCCAGCTGCT	154214
rs549073751	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981891	AATTTGGCCGGGCGT[A/G]GTTATGGGCACCTGT	154214
rs549086916	in-del	-/A	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085659	AATATATACTACTTT[-/A]AAAAATTGAACTATA	154214
rs549108118	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017507	CTATACAAAACAAGT[A/G]TATGAATGGCTAAAA	154214
rs549108710	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125044288	TGGACAAAAGAGATT[G/T]TAATGCCATGAATAT	154214
rs549135210	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086866	TGTTCTGTGACTCTG[A/T]CTATCTCTTGAGTCC	154214
rs549150710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004051	CTAATCTTTCTTTAA[A/G]TGAGGGGTTACAGTT	154214
rs549193732	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997024	GCACTCCTGCAAGTT[G/T]AGGTTCTACAAACAC	154214
rs549202975	snp	A/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124988879	AGCCGTATCTGTATG[A/T]CAGTTGACATGTAAA	154214
rs549237776	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124981268	CTGGAATTTTTCCCC[A/G]TGTGAACACAAAATA	154214
rs549256836	in-del	-/TTC	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125075215	TGTGGCCCAAGACAA[-/TTC]TTCTTCTTCTAGTGT	154214
rs549267530	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060234	GGAATTTGAGTAAAA[C/G]AAATGAAGAATTTCT	154214
rs549306557	snp	C/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124977848	ACATGTTCAGGTTAT[C/T]AGGGAGTTGCAGAGA	154214
rs549407645	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990834	CTTTGAGAGGCTGAG[A/G]TGGGAGGATTACTTG	154214
rs549478955	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011705	CACCTTTAATTTTTT[A/T]AAAAATGATTTACTA	154214
rs549482916	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960688	TGGCATCCATTATTG[A/T]TACTCTGGTCTTAGC	154214
rs549501632	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026861	AATGAACTGTGATAT[A/G]CTAGTTATAGAGTAG	154214
rs549520616	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039332	AGACCTTAAACCAAC[A/G]AAGATCAAAAAAGAC	154214
rs549546586	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124975928	TCAAGATTTTTAAAA[A/C]ATATTTTTCCTATGT	154214
rs549563079	snp	C/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125020124	AGACAGAGCTGTTCA[C/T]GAGAATGATAAACAG	154214
rs549582035	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032835	TTAAGTAATGTAAAA[A/G]AGATGATTGTAGAAA	154214
rs549680791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046076	AGGCTCTAGGATGTC[A/G]GGAATGGCTTCACAG	154214
rs549686137	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124994012	TTGCATTTGAGAAAA[-/C]AAATTACTCTGGCTG	154214
rs549703859	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990164	GTCTTCATTTTCTTC[A/C]TTCCACACTGGATAT	154214
rs549751944	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071126	TAAACAACTTGAGGA[A/G]GACAGGTACTATTTT	154214
rs549758904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032095	AGCATGGGAAAGACC[A/G]GCCCCCCATGATTCA	154214
rs549791507	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982826	ATGACTTTATGGTAT[G/T]TGAAAGTAATTTACT	154214
rs549829288	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125013206	TTTTGGAGATTATAA[A/T]TTAGTGAGAAGAAAC	154214
rs549831383	snp	A/G	0.00028394	0.0119117	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048189	TACCCCAGCCAACCA[A/G]TCGTGAGATTCATGG	154214
rs549833085	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073458	TTTGCTTAAAGAAGG[A/T]TTCTCAAATTAAACA	154214
rs549852235	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054881	CTGCAACCACACTTT[A/G]AGCCACAAGGACAGG	154214
rs549893227	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006724	GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA	154214
rs549969828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977026	TTTGTTAAAACAAAC[C/T]GTTCATACATGCTTT	154214
rs550002138	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969873	CTATAGTTTTGGGGG[C/G]GTTGTCATGGAGGAT	154214
rs550013925	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091000	AAAAGAAATTGCAAA[A/G]GAAAAATTACGTTGA	154214
rs550052246	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125068115	CTGTGTGTTGGTACT[G/T]TGCACAGCTCTTTAA	154214
rs550055701	snp	C/T	1.66893e-05	0.00288867	intron-variant	RNF217	GRCh38.p7	6:125076633	CTAACTCTTTCCTTC[C/T]CCTTCCCTCTCTTGC	154214
rs550057505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069769	AGCAATAGTGTATAA[A/G]CATTCCCTTTTCTTT	154214
rs550072408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005996	AGAACTTGGTAATGG[A/G]CTGTTAATTAATTAA	154214
rs550089785	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970552	ATGTGCCTTTTAGAC[A/G]TTCATGAAGGGATGT	154214
rs550098297	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034578	TTTGGTACCAGTACC[A/T]TGCTGTTTTGGTTAC	154214
rs550118860	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125070224	TATTCCATGGTGTAT[A/G]TATAGCATGTTTTCT	154214
rs550123252	snp	A/C	0.019998	0.0979748	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971558	CATCCCAGGTTCAAG[A/C]GATTCTCCTGCCTCA	154214
rs550126432	snp	A/G	0.000165851	0.00910484	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963232	CTGGAGTTCTACCTG[A/G]CGCCCGAGCCGTTCT	154214
rs550146999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985862	ATTTATTAATAAAGG[A/G]GTGTTGTGAACATGG	154214
rs550154091	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045678	TTGAAAATTAATCTA[A/G]TAACCTTATAGGAAG	154214
rs550161871	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971908	CTTCTCACTTTGTAT[A/G]CTGTTAGTGGGGCCA	154214
rs550179676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028361	CTGTTTGCCATTTGT[A/G]GGTCTTCTTTTGAGA	154214
rs550187991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978373	CCCACCGTGGCTCTG[C/T]GCTCAGCCCATGGAT	154214
rs550250055	snp	G/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB, downstream-variant-500B	RNF217, RNF217-AS1	GRCh38.p7	6:124964999	TAGTCATTGTGGCTT[G/T]GGGTACTTTACCTAG	154214
rs550256269	snp	C/G/T	4.74485e-05	0.00487052	intron-variant	RNF217	GRCh38.p7	6:125082425	GGACATTATGTAATA[C/G/T]ATATTATTATCTGTA	154214
rs550276973	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033791	TTCCACAATGGTTGA[A/G]CTAGTTTACAGTCCC	154214
rs550300349	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984817	AAAGGAAATGACTCA[C/G]CTTTATTCCCTCTAA	154214
rs550313666	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999256	TTTTAATCTGCCCGT[C/G]TCATGAGTTTCTAAC	154214
rs550314388	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125029276	GAAGGTATTAAACAT[C/G]AAAAGCAAAGACAGC	154214
rs550315381	in-del	-/C	0.00678093	0.0578315	intron-variant	RNF217	GRCh38.p7	6:125051442	TACATTTCTTATCTA[-/C]CACCCTCTGTGCTAC	154214
rs550326414	snp	A/C	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125063691	TTATAACATAACAGG[A/C]TTGGTAGTATGTAAG	154214
rs550371635	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088384	AAAATAGAACAAATA[A/C]ACATTTCATAGCCAA	154214
rs550386939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993405	TCCACTAAAATTATT[A/G]TCATTAGCCCATCTG	154214
rs550387770	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056431	AATAAACGTGAAAAT[C/G]TTTTAAGCCTTATGA	154214
rs550428630	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008028	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	154214
rs550483119	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125029433	ATAGAAGCCAGGAAG[C/G]AGGAAATTATTTCTT	154214
rs550509374	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063225	AGAAAAGTTTCTAAG[A/T]CAAAAATTAAAAGTG	154214
rs550514147	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987465	TCCTGGACATTTTAT[A/G]TAAACAGAATCATGC	154214
rs550517740	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124978942	GAGTCCAAGGTTTTT[A/C]TGGGCTTGGAATGGG	154214
rs550601805	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988053	GAGCGAGCATTACCA[C/T]CTGAGCTCCGCCTCC	154214
rs550610701	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124966470	TTAGGTTTGACAGAA[A/G]CAAATGTGTCAAGCC	154214
rs550629209	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036043	TTAAGCCCCGCATGC[A/G]ATAGTTATTTCTCCT	154214
rs550674087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077488	CCTCTTCCTCAACAA[C/T]ACATAGTAGCCTCAT	154214
rs550697966	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125007309	GGTGTGCAGTGGTGC[A/G]ATCTCGGCTCACCGC	154214
rs550736469	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124979723	ATGATGGTAAATCTT[C/T]GGACAGTTTGCTTGA	154214
rs550737614	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008479	ATCGCATGCATACTG[C/T]GAGTTTGAATATCCC	154214
rs550738980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016794	TGTGAGGGGGTGGGG[A/G]GCAAGGGGAGGAATA	154214
rs550773244	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124973067	ACAGTAGGAGCTAAT[A/G]TCGTCAATATGTAAA	154214
rs550799196	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125041927	AAAGTAAAAACACTG[A/C]AAATTAAACTATTGT	154214
rs550799253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049846	AATTGACTATGTCTG[A/G]AAGAGGAGGAGCAGG	154214
rs550800597	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001001	ATTCTAAAATGACCT[G/T]GGAATATAGAGTCTG	154214
rs550840911	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033444	GTGAGAACATGCGGT[A/C/G]TTTGGTTTTTTGTCC	154214
rs550847273	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006906	ATGAGCCGAGATCGC[A/G]CCATTGCGCTCTAGC	154214
rs550862184	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042493	TTTGGTTCAGTGTAG[C/T]AGGATAGGGATTTTG	154214
rs550864510	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125001821	TTTTCTAATGCTGAG[C/T]GGAATGATTCAAAGC	154214
rs550916102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058192	TGAAGGGAATTATAA[C/T]TGTCTTAATGCAGGT	154214
rs550944191	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125036510	TCGCAACAAAAGCCA[A/C]AGTTGACAAATGGGA	154214
rs550965881	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044328	TTGTTCACTACTTAC[A/G]AAAAATACTCTAGCT	154214
rs550967919	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125059164	TATTGTATGAAATAA[C/T]GTGTTGCATTTTTAG	154214
rs550969576	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050367	ATACAATGGCACTTT[C/T]GATGCATCTTTCACC	154214
rs550992017	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002207	GAAGTGCCTTTCTGT[A/G]TGGTCTGTTGCTACT	154214
rs551029102	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045125	TTATTGCGGTCATGA[A/G]ATAAGTAATACTGTA	154214
rs551029219	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037326	GGAGTAGCTTTTAAA[C/G]AACAAACTACCAGCA	154214
rs551037816	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124993006	TTATAGACTGAGAAA[C/G]AACTGTCAGTGCTCT	154214
rs551062970	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977906	CTGGCTAAGACTTTC[C/T]TTCTTTTTACTGTGG	154214
rs551064739	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125043794	AGAAAAAAGTGTTTG[G/T]GCACATATTTTTAAA	154214
rs551117894	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973684	ACCCCAATGACTTGC[A/T]TCAATCCAGTGAACT	154214
rs551156214	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125065308	AAAAAAAAAAAAAAA[A/C]AAGTCATGGAAATGT	154214
rs551196472	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125079120	CATGGTCTTCATTCC[A/G]TGTAACCACGTGCTC	154214
rs551218620	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030982	CTACATCTTCTGAAA[C/T]GTAGGTGGAGGTTTC	154214
rs551220043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065842	AGTCGGTAGGCAAAT[C/T]GTAAAGTTTTGGGGA	154214
rs551329911	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968074	GGCATGAGCCACCGT[A/G]CCTGGCCCCATAAAT	154214
rs551343977	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125003063	AGATTAAATGGCCTA[A/C]CTTAGTAAGTAGTGA	154214
rs551365014	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960958	CTTGGGTCAGACCGA[C/T]AGATGACATGGCATT	154214
rs551366793	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969040	TGATGGCATAAATAA[C/G]CTTTTTTTTAAAAAA	154214
rs551384223	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125073144	AAAAGTTGAATGTAC[A/G]ATGCTTTGGGTTTTC	154214
rs551400639	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125025993	GGTAAGAAAGAAGCA[C/T]CCCAGAGGGTCCCAG	154214
rs551401155	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125037060	TAATGGATATTAAAC[C/T]AACAGCACAATTTAT	154214
rs551422413	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124995838	GAGCTAGGAGAATCA[C/G/T]GTGAACCCAGGAGGT	154214
rs551427994	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002746	AACTTCATATCCCTT[A/G]TATGGAAACTTTTCC	154214
rs551449897	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124976231	TCATGTATTACCGGC[A/G]TAGTTTCTTCCCTCC	154214
rs551454751	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961724	TTATTTCTCTGAACT[A/C]GACATCCTAAATAGC	154214
rs551463105	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983076	TATATTTCTTCTTCA[A/G]CGCTCCCCCCTCAAC	154214
rs551514303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989001	ATCACCAAAATGCTA[A/G]TAGTCTTAAACCAGT	154214
rs551528747	in-del	-/A	0.138207	0.223612	intron-variant	RNF217	GRCh38.p7	6:124989867	ATTGTTCTCTGCTTG[-/A]AAAAAAAAAACACCA	154214
rs551592442	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981961	TGAACCCGGGAGGCA[C/G]AGGTTGCAATGAACC	154214
rs551600997	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089747	TATGCTGTCATTGGT[A/T]CTCTGCGAATCTGTG	154214
rs551601134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980204	TGGAAACATCTTTTG[C/T]GAAGATGTCCATAAT	154214
rs551602694	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125025423	CATGCTTATCAGTTT[C/G]AGTGTCTGAAGTTAG	154214
rs551608951	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990296	TCACTACTCTTATTA[A/T]CTTATCCAATTTCTG	154214
rs551636573	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091424	TGCTAAGGAGAAAGC[A/G]TATCTTTAGGGATGT	154214
rs551675646	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125010336	AAATATGTTCAATTT[G/T]AGTTTCAATTGATTC	154214
rs551679946	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087018	CATTTTTCTCCATAC[C/G]TCTGCTATTCTAACT	154214
rs551707357	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124973780	TACCTGTTCTGGTTA[C/T]TGTCTCCTGTTTAAC	154214
rs551729050	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124983945	TCCTCATGCATGGCA[C/T]CTTCTATGCATCCTC	154214
rs551768833	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125012835	TCTTATTTATATGCT[A/T]ATGTTTTGATCACTA	154214
rs551777669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011803	TTTCTTTTCTTTGCT[C/T]ATTTTCCTCTGTATC	154214
rs551777748	snp	C/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125019212	CACCATTTGAAAATC[C/G]CTTCCTTTGAAAATC	154214
rs551794684	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984586	AAAATAGAGTGGAGG[A/G]GAGGGGACATTTCAA	154214
rs551837140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012304	GTTTGAACAGCTTAT[A/G]TGACAGAATTTGGAT	154214
rs551891600	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125020564	CTGGTTGTTGTTGCC[-/T]TTTTTTTTTTTAAAT	154214
rs551927976	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961714	ATCCTTAGCATTATT[C/T]CTCTGAACTCGACAT	154214
rs551930858	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013859	TCTAAGGCAAAGGAC[A/G]TGTAACAGCAGCAAC	154214
rs551945651	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046219	GAGCTGGTGGAGAGT[C/T]GGGAGAGGCAGCTGA	154214
rs551962968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978000	GCTGGCGTATTCTTA[C/T]TCTGTTAAAGATAAA	154214
rs551993316	snp	G/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960838	CAATAAGCACTTAAA[G/T]TATCATTTGGAGAAA	154214
rs551999603	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020993	ATTACTATCATGGAA[C/T]GTAAATAAACATGGC	154214
rs552035273	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994175	GTATCTTTTTGTTTT[A/G]TAAATGTTTAAACAT	154214
rs552052658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970677	TTAGACTGGATGAAG[C/T]CACCTGTGGAGGGAG	154214
rs552055568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007307	CTGGTGTGCAGTGGT[A/G]CGATCTCGGCTCACC	154214
rs552074053	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125023915	TGTTGGTTACCAGGG[A/G]ATGGGCATGGGGGGA	154214
rs552116888	snp	A/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125074337	TAGATAGATAGATAG[A/T]TAGATAGATAGATAG	154214
rs552160019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977128	CATCCAAATGAAGAG[C/T]TTCAGAGGGAGTTAT	154214
rs552195269	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033425	GTTCAGTTCCCATCT[A/G]TGAGTGAGAACATGC	154214
rs552218710	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125034674	GGATTGGCTTGGCGA[C/T]GCAGGCTCTTTTTTG	154214
rs552219397	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B, missense, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964809	ATTTCGCTGCCCTGC[A/G]ATGGGATTCAGACAT	154214
rs552228054	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068252	TGTAGAGTGAGGAAT[A/G]CTGCAACAGGGCTAG	154214
rs552249031	snp	A/C	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124999398	AATTCCTGTAAGTGT[A/C]TCTCTTCTCTCATCT	154214
rs552279888	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035122	TGGGGTTTTCTAGAT[A/G]TACAATGATGTCATC	154214
rs552336727	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124992539	GGATTCGGTTAGCTT[C/G]TTCTAGTGTATTATA	154214
rs552350441	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125070043	CCAAACTTCATGAGA[A/T]CATCTTTATACCTTT	154214
rs552362404	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062664	TCACTGCAACCTTCG[C/T]CTCCCGGGCTCAAGA	154214
rs552388847	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125051342	TCTCTGATGGCCCCC[A/G]AGATCGTGTGTTAAA	154214
rs552389312	snp	C/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006852	TACTCGGGAGGCTGA[C/G]GCAGGAGAATCACTT	154214
rs552427531	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049833	AAAGGAGGGGTAAAA[C/T]TGACTATGTCTGGAA	154214
rs552456268	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087283	ACTTTACTACAAAAA[C/T]AAGAAAATGTATGCC	154214
rs552467129	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998997	TTTGTTTTCAAAAAT[A/G]GATACATGTAATTAT	154214
rs552484454	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125029542	TTTTGGCATGAAAAG[C/G]CTCCGTTGAAGTTTC	154214
rs552490257	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964059	AAGAGAGGCTAAGAG[A/G]TTTCTCAGAACAAGC	154214
rs552500512	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071345	CACCCGTGCCATCAC[A/G]AGGGTGAACAACTGA	154214
rs552525183	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070316	TGCTGCTATAAACAT[G/T]TGCGTGCACATGTAT	154214
rs552535794	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124997784	TACTTTCTCACCTTT[A/T]GTTGTCTCTCCCTCA	154214
rs552539021	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091528	TTCATTGTTCATTTT[C/T]AAGCTAACCTATACA	154214
rs552539925	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028384	TTTTGAGAAATGTCT[A/G]TTCAAATCTTTTGCC	154214
rs552546451	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084745	GACATTTATGGTTTG[A/G]GAATAGCATATTTCT	154214
rs552550147	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125051183	CTGATATTTTAGCCT[A/T]CACTTCACCTAAAAA	154214
rs552560362	in-del	-/AG	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125030255	TTTCAGTGGGGGCAC[-/AG]AGCCAAACCATATCA	154214
rs552587127	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054717	TGGGCGATGCAGTCA[C/T]ATGGTATAGAGCAGT	154214
rs552592930	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972005	CCCCAGTCAAGTGTC[A/G]TATAGCCATCTCTCT	154214
rs552601442	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083281	GAGAATTGCTTGGAC[C/T]GTCTTTGAACTCTGC	154214
rs552621774	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030779	CGGTGCAAGCTGTCG[A/G]TGGATGTACCATTCT	154214
rs552627887	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993297	TCTTGGGTTTTCTGA[C/G]TAAGCGAACAATATA	154214
rs552642147	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076269	ACTGTTTATCTCTGC[A/T]TATTCCCCCAAGTTG	154214
rs552644092	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091898	TGCTCTTCTTGATCT[A/G]TGCCTTTTGTTTTAG	154214
rs552648060	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970336	TAGAGTGATACAGGC[A/G]AACGCAGTTTGAACT	154214
rs552648136	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005810	AATATGGTTTTGTAT[A/G]GAACATAAGGTATTA	154214
rs552669371	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986437	TTTTACAAAGATACT[C/G]TAATGCATGGCTTCC	154214
rs552673974	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999832	CATACTTTATACTTA[A/C]TTATTTCTCTTATAC	154214
rs552699294	in-del	-/TTTTTGTTTTC	0.0119091	0.0762411	intron-variant	RNF217	GRCh38.p7	6:125025368	ACAATCCTAACGAGT[-/TTTTTGTTTTC]TTTTGCTTTTATAGT	154214
rs552711921	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978450	AGATGAGGGGAATGC[G/T]GTGGTGCCTGATAAC	154214
rs552715733	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994206	ATTTTTAAAATATAG[A/G]CAGAATAGTCTAACC	154214
rs552775310	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125079340	GTTTTAAATCAAGTC[A/G]TATAATTTTTAAGAA	154214
rs552778902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986890	ATTATTTCTTTTGAG[A/G]TAATGTTTTGCTTGC	154214
rs552779676	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125057448	CAGCCTCCCAAAGTG[C/G]TAGGATTACAGGCAT	154214
rs552813713	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979053	CCAATAGAGAGAGAG[A/T]GTGTAAGATGGTGAT	154214
rs552828417	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961200	ACATGAATGTGTAAA[C/T]TGAATTCCCTCTCAG	154214
rs552853263	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125022933	TCTTTTTGAATTTCA[A/G]CAATTATTTCTTAAG	154214
rs552872297	snp	C/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125077202	ATATCCAGCAGCAGG[C/T]CGTACACATATCCTC	154214
rs552882238	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015727	GTAATGTAAAAAGAG[A/T]CATGACTTCTCAAAA	154214
rs552882791	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993808	GAAGGGGCTGCGTAA[A/G]GAGTGTGTCAGGGCT	154214
rs552910106	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998709	AGGAGGCCCAGGCAG[A/G]AGAATCGTTTGAACC	154214
rs552922056	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015536	AGCTATTTTAGAAAA[G/T]AAAAGCGGTTATGAT	154214
rs552956017	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124995606	TGAATATAACCCGAT[G/T]TACTTACACTTTGCC	154214
rs553004789	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009000	TTAATGGTTGAAAAT[A/G]ATATATTATTACATG	154214
rs553020395	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042014	CTTTTAAAATGCATT[A/C]TTGAATTGATGAAAT	154214
rs553066714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965309	CCGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA	154214
rs553068108	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009691	GATCCCTCTAAAAAC[A/G]TAGACAGATATCAAA	154214
rs553089433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035004	CTCTCTGTTTGTCTG[C/T]TATTGGTGTATAAGA	154214
rs553122668	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025960	AAGGCCTTGAAGAGG[A/G]AGGTGAAATGGTTCA	154214
rs553131552	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002416	CTTCCATTTCTGTAT[A/C]CAAATGCTGTCGTGC	154214
rs553150855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035493	AATACTTTACAGACT[A/G]TTTTTCTTATGGGTT	154214
rs553189126	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050069	AGGAGGTGATAGCAG[A/T]TCTTTATGGAAGAGA	154214
rs553193878	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125060726	CTGGAATTACAGGTA[G/T]GAGCCACCACGCCAA	154214
rs553237199	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070971	TGTATACTGATTTAG[C/T]CATAAAACATTGTAG	154214
rs553265949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023183	AAAGAATTTGATGTC[C/T]GAGGTAAGACCTGAA	154214
rs553275643	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125030056	GCATTTCTTACATGG[C/T]AGCAGCAAGAGAAAA	154214
rs553285313	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994375	TGTATCTCCCTAAAG[G/T]GAGGACTTATTCTTT	154214
rs553301012	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125030796	GGATGTACCATTCTG[G/T]GGTCTGGAGGACAGT	154214
rs553308355	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125009082	AAGGAAGTAGATAGA[A/C]TGTGCTTTCCTGAAC	154214
rs553343619	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966028	GGCTAGGAAGTGGTG[G/T]TCTGCATTGGCACTA	154214
rs553343840	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:125079065	TTGGCCAGAGGCAGA[A/G]AAAGGGCCTTCATCT	154214
rs553359730	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088837	ATATTCTGTCACTCT[A/G]TTCCATTATTAATAC	154214
rs553362575	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125031032	TCTTTGCACATGCAC[A/G]CGGAACACCACATGG	154214
rs553378901	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057654	GAGCCTTCAGGTTCA[A/G]TCTGGGAGACTGCAC	154214
rs553439058	in-del	-/TTTGT	0.101562	0.201162	intron-variant	RNF217	GRCh38.p7	6:125052331	TGTGGTTTTATTTGT[-/TTTGT]TTTGTTTTGTTTTGT	154214
rs553445368	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989155	TGTGATGGAATTTTT[A/T]TTTAATTTACTATTT	154214
rs553492464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050485	CTTATAAACCCTCTG[A/G]GTAGAAATTACATTT	154214
rs553583279	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051887	GGGAAGAATTTTCCA[G/T]TACCCTTTGTGTTCA	154214
rs553604947	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028766	GCTTTTTAAAATAAG[A/G]TTTTTTTTTTAGTTT	154214
rs553616835	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125076960	GAGCACCTGCCATGT[G/T]CCCAGTGTTCAGAGG	154214
rs553619259	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124999838	TTATACTTACTTATT[A/T]CTCTTATACAGATAA	154214
rs553664602	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088014	ATAAGTTACAAAATT[-/C]TTTTTTTTTTTTTTT	154214
rs553681385	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125018296	ATTTTTATAAGATCA[A/C/G]GTGACTAATGGAAAT	154214
rs553717450	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087082	GGAGGGGCCTAAAAA[C/T]TCACTCTGGTATGTG	154214
rs553724634	in-del	-/ACACTG	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124973198	AGATCCCAGCTCATA[-/ACACTG]TGGATAAGATTTGGC	154214
rs553762349	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980915	TATGAGAAAGCCTCA[A/C]GTATTTGTCTTTAAA	154214
rs553781524	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961025	CTCAGACACACATAT[A/G]TGATGGAAATGTTCT	154214
rs553798014	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089223	TCAGAGGGCCTAATA[A/G]TAGTCTAAAACCAAG	154214
rs553800969	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024930	GGAGTTGAAACCATG[C/G]GAGTGGAAGAGTAAC	154214
rs553815799	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125074273	GAAACTCTCCAGTTA[G/T]GTAGGTCGGTAGACA	154214
rs553835358	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066221	TATCTCATTCTTCAC[A/G]ACGTTCTTAACCCAG	154214
rs553906129	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983077	ATATTTCTTCTTCAA[C/T]GCTCCCCCCTCAACC	154214
rs553906488	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967612	TAGATACAAGCAACA[C/T]ATTTCTTCTACAGAT	154214
rs553958110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039049	CCCCATCCCTGCTGT[A/G]TCCATGTGTTCTTGT	154214
rs554001229	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022035	CACAAGCATGCACCA[C/T]CACACCTGGCTAATT	154214
rs554111968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074412	ATTTTTGTGATTACT[A/G]TGATTAATGGCCGTT	154214
rs554199857	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020429	TCTGTGAGCATTTGG[C/T]ATTCACAAGTCCGCC	154214
rs554202277	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006253	TGAACTTTTGACTCG[A/C]GTTTCCAAAATTCAC	154214
rs554224564	snp	C/T	0.00517822	0.0506191	intron-variant	RNF217	GRCh38.p7	6:125019465	ACTATATAAGCAACA[C/T]TTTTTATTGCTGAGT	154214
rs554229626	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024380	CTGAGCTCAGGAGTT[C/T]GAGACCACCCTGAGC	154214
rs554263493	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013461	GACCTGAATGATGCA[A/C]GAAAATGAGTCATGA	154214
rs554265709	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006903	GCAATGAGCCGAGAT[C/T]GCGCCATTGCGCTCT	154214
rs554266470	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125078333	CACAAAATCACTGTA[-/T]TTTTTGCATTGTTAT	154214
rs554277701	snp	C/T	1.88517e-05	0.0030701	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962927	AACAGCAGGAGGCGC[C/T]CCCCGGCGAAGAGCT	154214
rs554280995	snp	C/T	0.000103141	0.00718051	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048205	TCGTGAGATTCATGG[C/T]CACAGTATGGCACCC	154214
rs554289404	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031792	CTCTGCCTGTTACCT[A/G]GTTCCAAAGTTGGTT	154214
rs554356709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032324	ACTTAAAATTCCTAA[C/T]TCAATTTTGATAGGT	154214
rs554387044	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067701	TGAAATGGCTGTGAG[A/G]GATATAGGTATATCT	154214
rs554413760	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026540	TAGAGCATTGAGAGC[A/G]TAAACGTGTCATCAG	154214
rs554415724	snp	C/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125019759	AGGCCTGCTACATTT[C/G]TCCAACACTGAAGCC	154214
rs554425318	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034265	TTAGACATGAAGTCT[G/T]TGCCCATGCCTATGT	154214
rs554431747	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969516	CACTACTATTTGCCC[A/C]ACCAATTTTGGGATA	154214
rs554442505	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045853	TATAAATGGTACTCA[C/T]TCATTTATTCAGCAA	154214
rs554453221	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090671	TTTGTACCAGATCTT[C/G]TCCATCATTTCATTA	154214
rs554481133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012856	TTGATCACTATATTC[C/T]ACTTCCTTTTCAAAT	154214
rs554488455	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125027848	GGATACAAGCTGTTT[C/T]AACTGGGGTGAGACG	154214
rs554489951	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125040506	CTGCTGAATTCTACC[A/G]GAGGTACAGAGGAGC	154214
rs554498327	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992066	ATCTTGTTAACATTG[A/C]AAATTCTGATTTACT	154214
rs554511893	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125061242	TATTTAGCACATATT[A/G]GCAATTTGCTTTCTA	154214
rs554550134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028786	TTTTTTAGTTTTACT[C/T]ATTATTTACTGTGTT	154214
rs554555674	in-del	-/AAACTCT	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125015451	TAGAGAAAACATGGA[-/AAACTCT]AAACGCTGAATGGTA	154214
rs554592124	in-del	-/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125019084	AAGCCCGCTTGCCTC[-/T]TGATCACAGAGATGC	154214
rs554629028	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125064247	TACTGATAAACCATT[G/T]TTAACTCTCCAGATT	154214
rs554646572	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963586	TTATTTAAGTGTATT[A/G]TGACCTCACTGGTTT	154214
rs554670989	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052820	TTACCATTTTGGTTA[A/G]TTTCTTTAGGACATA	154214
rs554674888	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090100	ATCATTTTCATCACA[A/C]TTGCAATCCTCTAGA	154214
rs554680616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022180	CACCACCATGCCTGG[C/T]CTGTTTTCTTACTGG	154214
rs554699333	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055788	TCATTATATTGGAAA[C/G]GAAGGCTCCATGTGA	154214
rs554699700	in-del	-/GGAA	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125025776	GAGGGAGGGAGGGAG[-/GGAA]GGAAGGAAGGAAGGA	154214
rs554740512	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991301	TGTCTGCATTAGGAC[C/G]TTTCCAGTAGCTGTT	154214
rs554751615	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125071349	CGTGCCATCACGAGG[G/T]TGAACAACTGATACT	154214
rs554761340	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125063301	GCAAATAAACAGTTA[A/G]TGAGCACTGTCACAC	154214
rs554772920	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056770	GAGACATTTTATTAA[A/T]CCATTGTAATCACAT	154214
rs554787998	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124994925	GGTATACTACGAGAA[G/T]TTTTTATGATCCAGG	154214
rs554802240	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125015019	TTTTATTTTCCCAGA[A/G]AGCCAGCAACATTGC	154214
rs554802818	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125002580	TTTTTAACCTTATTA[A/T]CTACGACCACAGCCA	154214
rs554824049	snp	A/C	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091604	TACTTTAAAACCATA[A/C]AAAATGCTAATTAAG	154214
rs554836248	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125049658	CACACATATAAATTA[C/G]TTAGCACCACATATG	154214
rs554867298	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992631	ATTTTGTTTCAGAAT[A/G]TGGATTTGATCTTGG	154214
rs554875379	in-del	-/ATT	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125000510	TTCTATAAAGAAAAA[-/ATT]ATTATTTTTTGAAAA	154214
rs554896181	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085977	GTATACTTTAACTTA[C/T]TGAATTAGTCCCCTG	154214
rs554901284	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049972	CTCAGGAGTGATTTG[C/G]TGGAAGTCATCAATA	154214
rs554903621	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124986000	CCATCAATGCAATAG[C/T]GTTAAGAGATGAGGC	154214
rs554930245	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084408	TCATCAGCAAACAGG[A/G]AAAAAAAAGACCCCT	154214
rs554957198	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978236	CTGTGCTGCTTCACC[A/G]GTCAGAAATCTCTTT	154214
rs554960450	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021347	TCTTGGCTCACTGCA[A/G]CCTGTACCTCCCGGA	154214
rs554968240	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125067060	GAATCCAAGGGAGCT[A/T]GGTTGTGGAGGATTG	154214
rs554974866	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125076315	TCATAGCATAAACAA[A/C]ATATACTTTCAAAGC	154214
rs555014317	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124978336	GGCTGCATTCCGCTT[C/G]TGCCCCAGACCAGAT	154214
rs555020655	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125042158	GATTGCATAGGTGAT[A/G]AGTAACACTATATTA	154214
rs555042430	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971288	CAAGTCTTCCAATCC[A/C]AGAAGGAGAAGACAC	154214
rs555051195	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077708	TTCTTCCCCTTTTTC[A/G]TCACATGGATGTCTG	154214
rs555059768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993594	TGTTTTTAAGTCAGG[A/G]AATTGTAGCCTATTC	154214
rs555077498	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971706	TGATCCTCCTGCCTC[A/G]GCCTCCCGAAGTGCT	154214
rs555090392	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035525	GTTGTCTGCATGTTT[C/G]TCATTGCTTTGGAGT	154214
rs555098636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987152	TTACAGTGCAGAATA[C/T]TTCCAATTGAAAATT	154214
rs555113374	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125063950	TGCTTTGGGCAAGAA[C/T]GTATTGATTCAAAGA	154214
rs555140071	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125015600	GTAGAGTATGATCAC[C/T]ATTTTACTTACGTTT	154214
rs555154646	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965169	ACAGTACAACCACTA[A/G]AAACTCCTCTGCAGT	154214
rs555159485	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125077743	AATTCCTTTTCTGGC[C/T]GTGTTTCTCATGTGT	154214
rs555167111	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972188	AACCTGGGGGGTCAT[C/G]ATTGAGCTATTCTTC	154214
rs555176096	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071365	TGAACAACTGATACT[C/T]ACAGTGGACTGGGTT	154214
rs555199827	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125007637	AGACATCTTTTGTTT[C/G]TGGTGACTAATGCTT	154214
rs555209523	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125078568	TGGGAGCCAAACTTA[A/C]CCTTTTGTCAGGAAC	154214
rs555261056	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008112	ATACAAAAAATTAGC[C/T]GGGCCTGGTGGCAGG	154214
rs555291584	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125061638	GTTTTCGTTTTTTTT[A/T]AAATTAATTGATTTG	154214
rs555304353	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048440	CTGCTAATGTCTGAC[A/G]TTTCTGTGCAATTTA	154214
rs555314738	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980450	TTATTGGAATTTTTT[G/T]GTAATTCTATTTAGT	154214
rs555330022	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092957	GACCAAGGGGCCTAT[A/T]CAGGGGTGGGAAAGC	154214
rs555345708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016437	ATATGAAATCAATGT[A/G]ATGGGTCATTATTGA	154214
rs555360954	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125042656	TGATTGGATGTTGGA[C/T]GGTATCCCGATGTGG	154214
rs555389620	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085102	CATATATACCAACGG[A/G]CTGAATAACATACTC	154214
rs555424426	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036150	TCTAATCGTTCGACT[A/C]CCACTTATGAGTGAG	154214
rs555426454	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976276	CCCTCCCTCCCTCCC[A/G]CTCTCTCTCCTTTCC	154214
rs555442264	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995230	TACATACAAAAGAAT[A/G]TAACACATGGTTATA	154214
rs555442327	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041646	CCCCATGTTCTCTGC[A/G]TAACAGGCCTTTCAG	154214
rs555463272	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125003375	GGTTTTTGGTATGTG[A/G]CCTTGGAAAAGTTAG	154214
rs555531197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995968	ATTTGGAATATTTCT[A/G]GGTTTTTTTTTTCTA	154214
rs555600860	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086490	TGTATGTTGCTTGAC[A/G]GAGGAACTTAATTAT	154214
rs555641972	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038969	GCATTAGCTGTTTCT[C/G]CTAATGCTCTCCCTC	154214
rs555668064	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125025063	GGATACAGGGGACAG[A/G]AAGAAGTCAGGAAAA	154214
rs555671037	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016869	CAAACGGCCATGGCA[C/T]GCGTATACCTATCCA	154214
rs555730641	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009855	ATGTTATATTACACA[A/G]TCTTTAAAAATGTTC	154214
rs555733400	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087962	TTTGTATTTAAAGTT[A/G]TAATTTAATTATGAT	154214
rs555802802	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989815	TATTGATTTTTCTCT[C/T]TATTGGATCTTTCTT	154214
rs555813522	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018510	GCATTTATAAAACTT[G/T]AGCTTTAACTCACAA	154214
rs555831015	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125071664	AGGGAATATCTAGCT[G/T]ATTCTGAACATTTCA	154214
rs555939008	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044525	TTCGTAGTCCTTTGA[A/G]TACATTAATTTTGTA	154214
rs555954341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989215	AATATTTTGATGAGC[A/G]CTTATGCTAGTAATG	154214
rs555956793	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125053380	GGGAAAATGAATTGA[C/T]ACATGTGCTTCATTA	154214
rs555982182	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067470	GGAGAAAAGAACTAG[A/G]TAAATATTATGGGGC	154214
rs555991143	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031041	ATGCACGCGGAACAC[C/T]ACATGGAAGCTGTCA	154214
rs556039769	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981668	TCTGTCCTGGACTTG[G/T]GAAGATACGCTATCA	154214
rs556059167	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125010813	CTGCTGTGCCTGGGT[G/T]TAGCAGAGAGAGCTG	154214
rs556084604	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961972	GCCAAAGGGGTGGGG[C/T]GAGGGGCGGCGAGGA	154214
rs556095312	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124987082	TTCATAATTTGGACG[-/T]TTTTTTATACGATTC	154214
rs556220326	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125059747	TTTACTGAATGTTCT[A/G]ACAACTTTCCACAGT	154214
rs556238641	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975802	CTCTTGCCAGAGATG[A/C]TCTTGGTGGAAAACA	154214
rs556250542	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074439	CGTTATTAGTTCACA[A/G]GCAGCCTCATGAGTT	154214
rs556266242	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089940	TCTTTCATTTTATAG[A/G]AAATTAGCATGCTTT	154214
rs556269574	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124968354	GTGTGTGTGTGCGTG[C/T]GTGTGTGTCTGGGGG	154214
rs556290720	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124966204	TAGTTGGTTAAAAAT[A/C]CAGGATTGTGGTTGT	154214
rs556313922	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075334	TGTATTAGTCCATTA[A/T]CATGCTGCTATGAAG	154214
rs556314406	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014577	TCACTGTAGCTGGAG[C/T]AATCAGCCTCCAGAG	154214
rs556353096	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125011478	TGCTCCAATTCCAGA[G/T]CCCCCTACTTTGTTC	154214
rs556381975	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124970329	TTCAGACTAGAGTGA[A/T]ACAGGCGAACGCAGT	154214
rs556395060	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984104	TACATGAATTTTAGG[A/G]AGAAGCAAACATTCA	154214
rs556420837	snp	A/G	0.0007328	0.0191275	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962995	GTCCTGGACGTGCTG[A/G]GTCAGCGGCGCCCGT	154214
rs556432913	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977499	GGTGTCAGCAAAATG[G/T]TTTATATCATTAATT	154214
rs556441723	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089251	AAGCTTCAGAAATTG[C/T]TTCGTGACTGTTGTA	154214
rs556497578	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125000142	TTACATCTCTGTTTA[-/T]TTTTTTTTTAGTGCT	154214
rs556498002	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997902	CTTACTGATCCCACC[A/G/T]CTTGAACTGTCCTTA	154214
rs556505685	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963671	GAAGGCACAAGATAC[A/G]AGTTGTTGCCCTCCT	154214
rs556507041	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125081342	CAGACTACTTAAAAA[A/T]TAATATACACTGTGG	154214
rs556525682	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032571	TAAGTTAAAAAAGGA[A/C]AAAATATGTATATTT	154214
rs556534358	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991695	TTGTAAATCATTTTT[C/T]CTATATCTAGAATTG	154214
rs556577917	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062791	CACGTTGACCAGCTT[A/G]TCTCGAACTCCTGAT	154214
rs556585955	snp	A/G	0.00716266	0.059414	intron-variant	RNF217	GRCh38.p7	6:124998474	ACCATTTTTCTATAT[A/G]CATTTTTTTAATATT	154214
rs556622188	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991179	ATGACTCTGTTCCCC[C/G]ACCCTGTTTCCTTTC	154214
rs556625368	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045524	CTTGTCGTGGGCATT[A/T]AGGGGGCATCTTTCC	154214
rs556641553	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125029492	ATGAACAGACCATTC[A/G]TAGAACTGGGTGGAT	154214
rs556643179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055231	AGTGAGAGATAGTAA[A/G]CAATCCAGTATGAGT	154214
rs556661914	snp	A/G	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124992137	CTACAAAGTAATGCC[A/G]GTAATGCTGACCTGC	154214
rs556662105	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999748	AACCTTTAAAGGAAA[A/T]AATTATCATGGACCC	154214
rs556750550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062250	TTAAGCATTACTTCT[C/T]TCTTAGTGAGTTTTT	154214
rs556754437	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124978130	CATGGTCCAGCTTCT[C/T]AGAAACTTTAGAGCT	154214
rs556785587	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027648	TCAATATACTGACTT[C/G]CTCTCTTTTGGGTAT	154214
rs556785662	snp	A/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125020555	GATGTGAGATCTGGT[A/T]GTTGTTGCCTTTTTT	154214
rs556868214	in-del	-/A	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125028631	AAGTGGAAAGAGCAT[-/A]AAATAAAACTGGAAA	154214
rs556882209	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034922	CTTCACATCCCTTGT[A/C]AGTTGGATTCCTAAA	154214
rs556896552	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125056654	TTCCAAAAAGGAAAT[A/T]CTAACTAACCTTTAA	154214
rs556943640	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028952	TGATCTATCTCAGTT[A/G]TAACATGTGAGAAAA	154214
rs556979726	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125007394	GGGATTATAGGCATG[C/T]GCCACCAAGCCCGGC	154214
rs556985801	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125055166	GAGTTGGCTATTAGT[C/T]CTTTTATGGTTTTAA	154214
rs556990424	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124978652	AGCTCCTTTATTCTC[A/G]TCGCCCACAGCTCAG	154214
rs556996529	snp	A/G	0.00953873	0.0683987	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967458	AGTACTTTAGATGAA[A/G]AAAGGAAGAGACATG	154214
rs557011767	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125047766	AAAATTTGCTTTGGT[A/G]TGAGGAGGAATTCAA	154214
rs557070957	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040568	AATTGAAAAGGAGGG[A/T]CTCCTCCGTAACTCA	154214
rs557150044	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085953	ATTACTGCATAATCC[A/G]TTGTAGGAGTATACT	154214
rs557155153	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087090	CTAAAAACTCACTCT[C/G]GTATGTGGGAAACAT	154214
rs557166264	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084062	GGTCAAGGTCTTACA[G/T]CATTTAATATCCTAA	154214
rs557190197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008173	AGGCAGGAGAATGGC[A/G]TGAACCCAGGGGGCG	154214
rs557209642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042729	CTGCCCTCTTTAGCT[A/G]CCTTGGATTGCTCTC	154214
rs557233460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077127	CTCTTAAATTTCTGA[A/G]ACCCTGTCGTAAGCC	154214
rs557240658	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076426	TATATTGGTCAAGAT[A/G]AGCCAACAGCTTGAG	154214
rs557252318	snp	A/C	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125029688	GAACGTGCATTTTTT[A/C]AAGTGTCAAACGTTG	154214
rs557252722	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125003848	ATGTCTTGTAGTCCT[C/T]ATAATCTTGTTAGGT	154214
rs557268999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036181	AACATGCAGTGTTTG[A/G]TTTACTGTTCCTGTG	154214
rs557285172	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972265	TCATCTTTAAAATAT[A/G]TCTGTATTCTTCTCT	154214
rs557287110	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007147	AATTGAATTATTTCA[A/G]TGAATGTGCTTCTTA	154214
rs557288417	in-del	-/AA			intron-variant	RNF217	GRCh38.p7	6:125050661	TTTCCCATATATAAG[-/AA]TGTGTAAAGCTTTCC	154214
rs557315027	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092478	ATATAAAGACACTCA[C/G]TCGGATGAAAACTAT	154214
rs557319560	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124975141	TTTTTGTGGTATTGA[-/T]TCTTGCTTTATTTAC	154214
rs557336378	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024891	GTGTTTTAACATGTG[A/G]GAGCTTGCACTGTAT	154214
rs557346979	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971726	CCCGAAGTGCTGAGA[G/T]TACAGGCGTGAGCCA	154214
rs557360070	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124985940	ATAAGTGCTGCAAAG[A/G]TCTGAATGTTTGTTT	154214
rs557422849	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004565	GGAAATTGCCTCCAA[A/G]GGTAGGTACAGAAGT	154214
rs557428316	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125064120	ATTCCTTAGTACTTC[A/G]TATATCACTACAAAA	154214
rs557430483	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972315	TCATTTCCCTCTCTC[A/G]GGCCTCTACCATTTC	154214
rs557469488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965270	TTGCTGGGACTTTCA[A/G]TAAATAATAATACAC	154214
rs557515247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979964	AAAAGTGTTGGAAGT[A/G]CATTGTCTTTAGTAT	154214
rs557544699	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050024	GTCATTGAACTTACG[A/T]AAATGAAAAAAATAT	154214
rs557558665	in-del	-/TTTGT	0.0806648	0.183917	intron-variant	RNF217	GRCh38.p7	6:125052327	GTGTGTGTGGTTTTA[-/TTTGT]TTTGTTTTGTTTTGT	154214
rs557595319	snp	G/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982291	TCAAAGTAAATTCAA[G/T]GTTTGCAAGAAGTTT	154214
rs557655786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125024680	AGCCAAGATCATGCC[A/G]CTGCACTCCAGCCTG	154214
rs557663951	in-del	-/TTG			intron-variant	RNF217	GRCh38.p7	6:125055890	CTCATCTACTTCAAC[-/TTG]TTTTCTTTTAAAAAT	154214
rs557694373	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058334	AGGAGGCCACATATA[A/C]ATATTGACTTAAGAC	154214
rs557708846	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974572	ACACTTAATATTATT[A/C]TGTATAGCATAATTT	154214
rs557718708	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964529	CAAACTGAACAGGGC[C/T]CCGTACCATGTGATT	154214
rs557728642	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065875	TGTGAGAAAAGCTAT[A/G]TATCCAAATAGCTAC	154214
rs557739353	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124987613	AATTAGTGTGAAAAC[A/G]GAGATCTTGCTTCTT	154214
rs557748629	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987873	GCAATATTAACTTGT[A/G]CATTCTGCGGTTTGT	154214
rs557774483	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125078122	ATGATTTTCCAGTGC[A/G]TGCCGCTTCTTAATT	154214
rs557796804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030763	GGCTTTTCCAGGCAC[A/G]CGGTGCAAGCTGTCG	154214
rs557819364	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980575	TCTTTTTTTATATAA[C/T]AGTGTTCCCTTCTGG	154214
rs557881049	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052539	AGAGATCCCCAAGTA[A/G]GCAGTGAAATATCAG	154214
rs557905877	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124973962	GCTGGCAGCTGATGC[C/T]GGCCGTTGTCAGTGA	154214
rs557966826	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125059589	ACTGGATTTGGAATG[A/G]GCACCACTGCAGCAT	154214
rs557975907	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016891	ACCTATCCAACAATC[C/T]TGCACGTTCTGCACA	154214
rs557978914	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982320	TTCTCTGTAAATGTG[A/G]TGGGATTTAATTTTT	154214
rs557994382	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997092	TCAAAAAAGAATTTA[G/T]TTTCTGTTTTGGTCC	154214
rs558015298	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983024	ACAGTAAAAGGATCA[C/G]TTCATAGAGTAATTT	154214
rs558039306	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125010002	TTTTTTTTTTTTTTT[A/G]CTAAATCTGAGGGTC	154214
rs558041637	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086403	TCATTTTAAAACTTG[A/C]GGGATTTAAATCAAA	154214
rs558048280	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975583	CTATAGGCGTGCACC[A/G]CCATGCCTGGCTAAT	154214
rs558110522	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003524	GATTGTAGGAATAAA[A/C]TTTAGAGATTCACTG	154214
rs558132302	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032244	AGGGTTAGGAGAAAA[A/C]CCATAATTCATTAGT	154214
rs558162617	snp	C/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081669	TAAAAGGTCAGAGGA[C/G]CGTGTTTCCTGTAGG	154214
rs558167628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996150	CCACAGCTGATGAAA[A/G]TTCCCATTGCTCCAT	154214
rs558169561	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125073592	GAAACATGAGTTTTG[C/T]TTTTCTTGCCCAAAT	154214
rs558183346	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012755	TATTTGAATAAAGTA[C/G]ATGTGATGCTTTAAT	154214
rs558197836	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026458	GCTATCATCATCATC[A/G]TCATCATTATCATTA	154214
rs558240934	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976534	CGGCCTCCCAAAGTG[C/T]TGGGATTATAGGTGT	154214
rs558248308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013391	TGTGTGTGTGTGTGC[C/T]GTTTTTGAGAGCATG	154214
rs558275881	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124969445	ATTTTTGCTTTAAAA[A/T]TTCAATGTGTATGGG	154214
rs558306945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080030	AGAGGAAAAAGAAAA[C/T]CAATGCTGTTACTTT	154214
rs558384700	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013788	ACAAGATTTTTAGTC[C/T]AGCAGATCTATTTCC	154214
rs558395116	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977590	TATGCTTTTGGCTTA[C/T]TACAATCTAAATGGA	154214
rs558397174	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025751	CTAGGGAGGGAGGAA[A/G]GGAAGGAGGGAGGGA	154214
rs558414824	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975965	TTTTCTTCCTCAAGA[G/T]ATTTTTTAAAACAAA	154214
rs558415597	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039760	AGTCTCTCAGACTAC[A/G]GTGCAATCAAATTAA	154214
rs558430334	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054279	CTCTTCCAGTTACCA[A/G]AAGCAGAAATGTACT	154214
rs558452390	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006165	AAGTGTGAATGAAGA[G/T]TGGAGCATAAAAGTA	154214
rs558461939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040425	ATAGACCAATAACAA[A/G]TTCTGAAATTGAGGC	154214
rs558470857	snp	A/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125033171	TGGATTTCAACTAAG[A/C]TCTGTTTGCCTACAG	154214
rs558492423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066839	CTGAATAAATAAATG[A/G]ATATACTTTTTCATT	154214
rs558530244	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034155	TAGGTTGCCTATTCA[C/T]TCTGATGGTAGTTTC	154214
rs558612019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060862	TGTACTTACTCCTAA[C/T]ATCTTATTGTGTGCC	154214
rs558626843	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069118	CTACACTTTAATGAA[C/T]TCTTGTCATTATAAA	154214
rs558635597	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005285	GTCTCAGGTCAGTCA[C/G]AAAAGTGCCTAAAGC	154214
rs558660534	snp	A/G	5.06804e-05	0.00503365	intron-variant, missense	RNF217	GRCh38.p7	6:125082482	ACTGGAACCTCATAA[A/G]TGGTAGAACCAGGAA	154214
rs558673324	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125061955	TTTTTCCAAATTGAA[A/G]CCATCTAACCCAATT	154214
rs558691086	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125062809	TCGAACTCCTGATCT[C/T]AGGTGATCCGCCCAC	154214
rs558710119	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995220	TGAAATATTATACAT[A/G]CAAAAGAATATAACA	154214
rs558714331	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997928	CCTTACCTGTTCTTA[C/T]GTGACGGTGACTCCA	154214
rs558719136	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075420	CCGCATGCCTGGGGA[C/G]GCCTCAGGAAACTTA	154214
rs558719968	snp	A/G	7.249e-05	0.00601995	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962880	GGAGGAGGAAGAGGA[A/G]GAAGCTGGGGATCGA	154214
rs558732207	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963728	ACAAGCTTGCTCAAA[A/G]GAGGAGAGGAAGAGA	154214
rs558748010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027744	AACTGTTGTCCATAG[C/T]GGTTGTACTAATTTA	154214
rs558754319	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125063276	AAACACAGGATTATA[C/T]GTTATAAAAGCAAAT	154214
rs558756973	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124998522	ACTGTGTAGAAGGCC[-/A]GGTGCCGTGGCTCAA	154214
rs558770265	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978217	TTGTGTTACAGGATT[C/T]CTTCTGTGCTGCTTC	154214
rs558777486	snp	C/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124996625	AATGAGGGGAAGAGT[C/G]AAGTTTTGTGTAACC	154214
rs558812382	snp	C/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125013070	CATACTTGAAATAAT[C/T]GACATTTAGTTCTGA	154214
rs558826136	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081813	GGCAAGTGGAATAGA[A/G]CCCAAATTTTCTAAT	154214
rs558888113	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125074555	GGAGTTAGGAACTTC[A/G]AAAACTTTTTATTCC	154214
rs558914720	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027233	CTATTGTGCTATCAA[A/G]TAGTAGGTCTTATTC	154214
rs558952341	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124991904	TAGCACTTTTCTGTC[A/G]TACCAGAAAGCTCTA	154214
rs558956965	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985459	ATAATCCAATTATAC[A/T]CTTAGTTATTTTGGA	154214
rs559042412	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984876	TACTATAAACTGAGA[A/C]AAAAGACAATTCACA	154214
rs559064321	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058972	CAATTACTTCTTGGA[A/G]ACTTAGCACCAGATA	154214
rs559070374	in-del	-/TAATT	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125019657	ACCAAATTAGACGAA[-/TAATT]TAGTTTCTCAAGTTC	154214
rs559098433	snp	A/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125021637	ACATGTAGAATAAAT[A/T]TATTCTACAAGGACT	154214
rs559114602	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124999459	CAATTGATCTTTACC[-/T]TTTTTTTTTCAAGCT	154214
rs559128266	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125013086	GACATTTAGTTCTGA[-/T]TTTTTTTCATTGTTT	154214
rs559133208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055353	GATCTGCAGTAGGAC[C/T]TGGTTGTTTATTATG	154214
rs559150373	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997688	ATGAGATACCTGGAC[A/G]CTAGTTTCAGGGTAA	154214
rs559172630	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050655	GAACTGTTTCCCATA[C/T]ATAAGAATGTGTAAA	154214
rs559196908	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125026968	ATTTGTTGAATGAAC[A/G]TGACATAATTTGTAC	154214
rs559199847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069514	GGCTCAGTAGTATTC[C/T]ATGATCTATATATAC	154214
rs559226301	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084279	TTTTGGGAAAGGAAA[A/C]AAAAAAGTGAAGGAA	154214
rs559244319	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971430	GGAAAGCTATGATTT[A/G]ATTTGATTTACTGTT	154214
rs559247681	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125014916	CCTTCCTAATAAACC[A/G]TGTTGACCCTGCTCA	154214
rs559249979	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087556	AATGCATACATTTCA[A/G]TGGAGACAGTATACA	154214
rs559254993	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:125007875	TTTAATACATATATA[C/T]CTCTTATAAAGTGTA	154214
rs559310532	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125007447	AGACAGGTTTTCTCC[A/G]TGTTGGTCAGGCTGG	154214
rs559317822	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008402	TCTGTACTTAGAAAG[A/C]AGTTAAGCATTAACC	154214
rs559331838	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964101	TTTCCTCCTCTGCTT[C/T]TATTTGAAAACTTGG	154214
rs559354659	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033436	ATCTATGAGTGAGAA[C/T]ATGCGGTGTTTGGTT	154214
rs559416299	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076503	AAGGATAATCTTGGA[C/G]GGTATGATTATAAGC	154214
rs559446971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029143	ATTACAAACTTTGCA[A/G]TAAGAGTTTGGAGTA	154214
rs559458232	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125048929	TAGAACAAGTGCATT[C/T]GTGAATTGAGAGATT	154214
rs559473687	snp	C/T	0.00795532	0.062565	intron-variant	RNF217	GRCh38.p7	6:125001707	ACAAAGTATAGGATT[C/T]CTCCCTTGTGTGATA	154214
rs559478010	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035995	ACATGTGCCATGGTG[G/T]TTTGCTGCACCCATC	154214
rs559478544	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086579	CAGAAAAATACATTA[C/G]ATTATGTACGATTTA	154214
rs559482699	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000225	AATTTAAATTGGTGT[G/T]TTAGTTTGTTTGCGA	154214
rs559488679	in-del	-/T	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125042504	GTAGTAGGATAGGGA[-/T]TTTGGAGCCTTGAGA	154214
rs559521552	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125041654	TCTCTGCATAACAGG[A/C]CTTTCAGTTCTCAAC	154214
rs559528658	snp	C/G	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:124970016	CGTGTGAGTTTCCAG[C/G]AATCGCAAGGAGATC	154214
rs559539571	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030019	GCTGGGGAGGCCTCA[A/G]AATCATGGCGGGAGG	154214
rs559547252	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971749	GTGAGCCACGGCACC[C/T]GGCCGATTTACTGTT	154214
rs559556541	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993343	ACAATAACTGGCAGA[C/T]AGTAATTACAAGTAA	154214
rs559584965	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964703	CTGAGAGACTGTTGT[G/T]TCTTTCATGCTTTAT	154214
rs559634636	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030812	GGTCTGGAGGACAGT[A/G]GCCCTCTTCTTGCAG	154214
rs559690584	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056268	GTTACCTTCAGCAAG[G/T]TATTTAATCTATCTG	154214
rs559698776	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065134	AAAAATAAAAGATAA[A/C]AAAAAAATTAGCTGG	154214
rs559731112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049757	TATTGAGAAGGGCAT[A/G]GGGGAGTAAAAAAGA	154214
rs559734700	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125052172	GGTGAATGCATTGTG[A/C]AATAAATAATTGTGT	154214
rs559738815	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084907	AAGGAGAATTTCTAA[A/C]CTGTCATAAGAGTAA	154214
rs559741292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070773	AGGTATCAAAAGTCA[C/T]TGAAGGAAACACATA	154214
rs559750279	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056998	AGGCCCGTTTCTGAC[G/T]GTTTTCTAAGTACAG	154214
rs559755000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000908	TTATTCTTTCTTTTA[C/T]ATGTAATGCCATGGA	154214
rs559772819	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053516	TTGAATTTGATAAGT[A/G]ATGATTTTGTGATTT	154214
rs559780866	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091932	TATACAAAATGCTAG[G/T]TTTGTTATATTCTTT	154214
rs559782274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022948	ACAATTATTTCTTAA[A/G]CACCTACTTTATGTC	154214
rs559793410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042305	TGAGTGGGCCATGAA[A/G]CTGGAATGCTCAACA	154214
rs559803059	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124993813	GGCTGCGTAAAGAGT[A/G]TGTCAGGGCTAAGAG	154214
rs559811641	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125056707	ATGCTGCAGTGACGT[A/G]ACATAGAGGAGCAAA	154214
rs559820758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058411	GAAAAATATAGCGTA[A/G]AAGTGATATAAAAGT	154214
rs559846030	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092745	TTCTACATTGGACTC[C/T]AGAAATGGAGGAGCA	154214
rs559907914	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084669	ATTCTTTCTGAATAA[C/T]ACAGAATAACTGTGC	154214
rs559911452	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125004721	ATGCCTAAATATATG[C/T]ACAAAGGACAAGAAC	154214
rs559935864	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065796	ACTACACATAGAATT[A/T]AAAACAGGGCACACA	154214
rs559949304	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125077853	CTCTCCTTAGCCCTT[G/T]GTCACTTCATGACTG	154214
rs559978126	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086809	AATTGTACTTTCTCT[A/G]CTGTGGTATCAAGAT	154214
rs559978575	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966895	CTCTATGCTCTGTAT[A/G]AAATTATAGTTTTGT	154214
rs559998489	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125050297	GTTTTCTTCAGACAA[A/G]ACTAATAATCCCCAT	154214
rs560001921	in-del	-/T	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124966184	ATACATAAAATAGCC[-/T]TTTTTAGTTGGTTAA	154214
rs560020398	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987962	TCCAAAGCCGTTAGA[A/T]TAAGTGTCCCCAATC	154214
rs560038187	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087362	TTAATGTGAGTCTTC[A/G]CATTGGATTATATTT	154214
rs560039459	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023441	TTGTAAAAAGAGTGC[C/T]CCAGAGAAGAGGGCA	154214
rs560101773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016616	GCACATAAACACCAC[A/G]GAATACTGTGCAGCC	154214
rs560107281	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124981214	TAAAACAGTCATTAA[A/G]TTTGTAATATCTCAT	154214
rs560132278	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081729	AACACTGTGATTCAT[A/G]TACCTTATAAAGCAT	154214
rs560140374	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966313	TTAATTTCCTCATCA[A/C]TGAAATGTAATTGCA	154214
rs560141967	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981888	AAAAATTTGGCCGGG[C/T]GTGGTTATGGGCACC	154214
rs560229303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975277	AAAACAGCAGGAAAA[A/G]TGAAACAATTGCTTG	154214
rs560259873	snp	A/C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009365	ACCTCCTGTGAAGCC[A/C/G]TCTCACAGACATAGA	154214
rs560266525	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976084	GGTATATGTGTATGT[C/G]TGTATATATGTATAC	154214
rs560323251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001831	CTGAGTGGAATGATT[C/T]AAAGCAAAGATAAGT	154214
rs560323362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125010187	GTATTTTGCTCTAAA[A/G]GAATGAAGATAGTGT	154214
rs560361243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995603	GTATGAATATAACCC[A/G]ATTTACTTACACTTT	154214
rs560384547	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002801	GTACTTACTGTGTAT[C/T]GTGGAATCTATTTGG	154214
rs560439305	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031193	TGTGGGCCCAGCCCA[C/T]GAAACCACTTTTTCC	154214
rs560463014	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979481	TGGTGACAGCAAGAG[C/T]CAGCAGAACAAAGAT	154214
rs560464807	snp	A/T	0	0	intron-variant	RNF217	GRCh38.p7	6:125037129	TTCATATGGAAGTGG[A/T]ATTGTTCTATTCTCT	154214
rs560478230	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090398	CAAAATTGTAAGGCA[A/G]TTTTATGAAACAAAC	154214
rs560480127	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125030912	CCCTAGCAGAGGTTC[G/T]ACATGAGGGCCCTGC	154214
rs560508408	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125068797	CAGTCAGCTTAGGAG[A/G]AATTGAGATGCAAGT	154214
rs560528171	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124999327	ATTCATTTCTTCCTT[A/T]GCTGATTCCCCAGCA	154214
rs560531839	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125018919	GGTGGTAAGTCTCCC[C/T]GGACTCCATTTGGCC	154214
rs560579964	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072584	AAGATTTTAGAACCC[A/G]ATGAAGCAATATTAC	154214
rs560597014	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012158	CAAGGAATAAAAAAC[A/T]ATGAAGGAATAGGAA	154214
rs560599372	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961315	AATACTTCCTGTAAA[A/G]TAAAGATAGATCAAC	154214
rs560622441	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025308	TAATCTTTCATTTGG[C/G]TTGGCTGCAAATGGA	154214
rs560639842	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059256	AAAGATATTTGGCCT[A/T]AAGTTTTCTTTGTTT	154214
rs560642930	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066379	ATGTCCCCACTCTGT[C/G]ACTCCTCTAGTCATA	154214
rs560651694	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997649	TTGAGCACATTCATA[A/G]GTCCTTGGAAACAGC	154214
rs560681152	in-del	-/A	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:124985764	TGGGAAGGAAGAGAG[-/A]GGTAGCAAGGAATTA	154214
rs560685978	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125018035	TTATAAGTGTAACAA[C/T]TATCCATTTCTAACA	154214
rs560688051	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967948	CAAGCCAAGCTAATT[C/T]TTTGTATTTTTAGTA	154214
rs560698911	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125060132	AGGAGATATTACTGA[A/G]TGAATTAATATTTGT	154214
rs560708138	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032808	TTCAGATAGTAAGGA[A/G]GGAAGAAAAGTTTAA	154214
rs560736127	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031700	ATTTTCATTAAAGCC[A/G]TTCAGCTAGTCTCTA	154214
rs560760241	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052890	CAGAGTTTCTGGACC[A/G]TGGTATATTTTGGGG	154214
rs560770960	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026821	TCATCTCCCTTACTG[G/T]ATGAAAAAAATGAAA	154214
rs560815931	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039281	CCAGGATACATGTAC[C/T]GAAGCAAGGGTTGCA	154214
rs560825345	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124990767	CCTTTGTAGAGTGAT[C/T]TCAAGAGTGAAGCCA	154214
rs560845973	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125000917	CTTTTATATGTAATG[C/T]CATGGATATTTCAAA	154214
rs560858952	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042899	CAGAGTAAAAAATTC[A/G]GGCTCTTAATCACAG	154214
rs560895624	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125044409	CCACACTTTGTGCTT[A/T]AATCTTTTATTGTAA	154214
rs560916651	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997631	GCAAAAACATCTGAC[G/T]CATTGAGCACATTCA	154214
rs560980177	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054785	GACCTTGTGAAAATG[G/T]GCACTTTTGGCTCTG	154214
rs560982061	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124996001	TCTCTTACAGACTAT[A/G]TACATGTATAGGAAT	154214
rs561002499	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990134	CTTTCTTCACTTGAC[C/T]TCAAGGACACCATAG	154214
rs561032590	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125068636	TATGCATATATATTT[A/G]TTTATACAGTTGGTT	154214
rs561082125	snp	A/C/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125046307	TGTAACTCTGTAAGC[A/C/G]TTAGAGAAATGTCAT	154214
rs561085051	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036037	TAGGCTTTAAGCCCC[A/G]CATGCGATAGTTATT	154214
rs561100581	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125048073	AAAGTTTATATAACA[A/T]TTTTCATCATTAAAC	154214
rs561111722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074755	ATTCAAATAAATACA[C/T]TGTATTAGGGGAAGG	154214
rs561143016	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125077264	CAGCATGGAGCGTAG[C/T]CTAGGAAGGCAGGGG	154214
rs561163351	snp	G/T	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963128	GGGCTCCGCCAGTGT[G/T]GAACCCTCCCAGCAC	154214
rs561168277	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124984415	TAACCAGGTGTGGTG[A/G]TGCATGCCTGTAGTC	154214
rs561185185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977852	GTTCAGGTTATTAGG[A/G]AGTTGCAGAGATTTT	154214
rs561218100	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970488	GTTGCCGTTTAATAA[A/G]ATGAGGAATAGTGTA	154214
rs561221290	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019959	TGTGGAGAAGAGCCC[A/G]GTAACCCTGGGCGAG	154214
rs561228378	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124993036	TTGCCTATAGTAGTA[G/T]TATTGGCAAATTTAT	154214
rs561289409	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124997535	TAGCTGTAGTAATGA[C/G]AGCAGACACATTGAT	154214
rs561327718	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125021566	ACTGCACCCGGCCAG[-/A]AAAATGCTTACCTTA	154214
rs561341533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040881	TGCAGAAAAGGCCTT[C/T]GATAAAATTCAACAT	154214
rs561388649	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992414	AAGAAACTAAGAGGC[A/T]ATAGAACATTGATTT	154214
rs561400422	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125034514	TAGTTGTAGATATGC[A/G]ACATTATTTCTGAGG	154214
rs561443555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999214	ATATTTCATTTTAAA[C/T]TTCCTCTTGTAGGAA	154214
rs561452820	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065403	CCAATATGAATGTCC[A/G]ATGCATTTAAAAATT	154214
rs561463815	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124979502	GAACAAAGATACCAG[C/T]GTGGCGCAGAGCACC	154214
rs561465638	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971845	CTTTCTTGTATTTTA[C/T]CATCTCTTAATGTTG	154214
rs561516946	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014289	AATCACTCACAGTTA[C/T]TGAGTTTGTACTGCT	154214
rs561564964	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022752	CAATTACACATTACA[C/T]GCTAGACAAAACAAA	154214
rs561629270	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993051	TTATTGGCAAATTTA[A/T]AGAGCATAATCAAAT	154214
rs561639098	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063681	TGCACAATAATTATA[A/G]CATAACAGGATTGGT	154214
rs561656513	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015376	TTATAAGTTTTTCTA[C/T]GAAAATAATCAGAAA	154214
rs561670672	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029327	CTTTTATTTTTTCAT[A/G]TTCAAATACACTTTG	154214
rs561684103	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000989	TATAGTGAAAACATT[C/T]TAAAATGACCTTGGA	154214
rs561691064	in-del	-/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967782	GTAACATAACATAAA[-/T]TTTTTTTTTTTCTTT	154214
rs561694681	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125004882	TTAGTCCATTTTTTG[C/T]TGCTATAACAGAATA	154214
rs561714058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986563	TTCAAATAGACTTTT[C/T]AAAAGTTGAATTAAA	154214
rs561731494	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021989	CAGGTTCAAGCCATT[A/C]TCCTGCCTCAGCCTC	154214
rs561745383	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001525	TAAAATGTGACAATT[A/G]AAATAATTAAGTAAA	154214
rs561811306	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038856	TTTTAAGTTCTGTGA[C/T]ACATATGCAGGATGT	154214
rs561812796	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125022561	AGCCAGGGGTGTGGT[G/T]GTTCCTTTAAGGGAG	154214
rs561828614	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070561	AGTAAGGTGGTATCT[C/T]ATTGTGTTTTTAATT	154214
rs561862299	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048019	TCTAGCAATGATTCA[A/G]ATAATTCCTGAAGCA	154214
rs561870163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009097	ATGTGCTTTCCTGAA[C/T]AGACGTGTTAGAAAT	154214
rs561891117	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125064361	AGCATGATTGTTTGA[C/T]GGCACATACTTTGGA	154214
rs561898071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057143	GCTTCATAGCAAATG[C/T]TGTTCTAGCAGTTTG	154214
rs561928623	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030055	GGCATTTCTTACATG[A/G]CAGCAGCAAGAGAAA	154214
rs561932181	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084845	ATCCATTTAACAGAT[A/G]TTTATTGAGTGCCTA	154214
rs561935881	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125064183	GCACATTCAGAGGCT[A/G]ACTACTTTCAAATAA	154214
rs561971926	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125066062	CTTTCATTTCCCATG[A/T]CTGGTGAGTCATTAA	154214
rs561990906	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008458	TTTTCTGCTCAGGGT[C/G]CATGAATCGCATGCA	154214
rs562003944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987406	CCTCCTATCCCCATC[C/T]TAAGAAACCATGAAT	154214
rs562008662	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024474	TGTAATCCCAGCACT[A/T]TGGGAGGCTGAGGCA	154214
rs562017079	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125050156	GTAGGTGCAATTCTG[A/G]GTTTCATTCTTATTC	154214
rs562042339	snp	A/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125011921	CTTTCCTCTGTCTTC[A/G]TATGCATTTTAGTGT	154214
rs562081927	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966863	AGACATAGCAAATTA[A/G]ATGGTGACTTAAATA	154214
rs562117539	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125052701	ATTCATCAAGACTCA[-/T]TTTTCTCCTCTCTAT	154214
rs562132659	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988691	GAGATTGTACTGAAT[G/T]TGTGTTTTCTCAATT	154214
rs562167211	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007043	ATTATTAAGTATGTA[A/G]ATAAAGTTCTAGACA	154214
rs562192451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036466	ATTTCTGGGTCAAAT[A/G]GTATTCCTGGTTCCA	154214
rs562210253	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016764	ACAGGGAGGGGAACA[C/T]CACACACCGGGGCCT	154214
rs562212650	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988015	TAGGAACCAGGCCAC[A/G]TAGGAGGAGATAATG	154214
rs562235640	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125051945	GAAATAGACCCAGAC[A/G]AATGCTTCTCTGGGC	154214
rs562244649	snp	C/T	1.64879e-05	0.00287118	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009315	AGAAGCCACATTTAT[C/T]TGTGCTGCAGGAGCC	154214
rs562254278	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071231	ATGATGTGAAAGTAA[A/C]ATGCGTTTGGTAGAA	154214
rs562319032	snp	A/G	0.0166325	0.0896639	intron-variant	RNF217	GRCh38.p7	6:125071538	TGTGTGTGTGTGTGT[A/G]TATCTTATTACAGGT	154214
rs562379380	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125059017	TGCCAGAAAATGTTT[A/C]AAATTTAAAAATTAT	154214
rs562381947	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974156	TTTGGTGAGGCAGTC[A/C]TAAGCCTGCCCAGAT	154214
rs562396232	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125011286	ATGATATAGGTAATA[A/G]TAATGGCCATCATTT	154214
rs562402869	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079652	TTAATATTGGACTTT[A/C]ATACTTAATGAATTG	154214
rs562432327	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017100	AAATCGTAGCTGTGA[G/T]TACAACTTAAAATTT	154214
rs562477302	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058453	TCTGCCACGTGTACT[A/T]TAATTACTTCTCAAT	154214
rs562487649	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125011750	TTTCTTTCATGGAAT[G/T]TTCCCATCTAGTTCT	154214
rs562488053	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968564	CAGCAGGACTTTTTC[C/T]GAGGCATGCTGCATG	154214
rs562493224	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125010383	CTTTTTAGGTATAAT[A/G]CATGAAGTGACTTGA	154214
rs562500657	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976665	CCACCACACCCAGCT[A/G]ATTTTTTGTGTGTGC	154214
rs562519431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003023	ATATTAAAAGGACTG[A/G]TTTAGTAATAATAGT	154214
rs562525114	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125064566	CATATTTTAACATGT[A/G]AATACTCAGATATCA	154214
rs562528426	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125073062	ACGACACTGCTATCA[A/G]TGTCAAATCAGGAAA	154214
rs562570589	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124976120	CATATGTATACATAC[C/T]GTTTGTCAAGTTCTC	154214
rs562583479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003668	CCACAATATATACCT[A/G]TATTAAAATATCACA	154214
rs562606199	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124973605	GGTAACTATTTGAAT[C/T]GGAACTTTTGACATC	154214
rs562635280	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983350	TGTGGGATAGAACTC[C/T]GACTGTGTACTTTAT	154214
rs562673044	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124996586	ACAGCTCTGTTGACA[C/T]TGGCTCTTGAAGGCA	154214
rs562720845	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125037749	AGTAGATCTATGTAT[A/T]TTTTGTGATTATTGT	154214
rs562729855	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982493	GTCATTGGTACCTCA[C/T]GTATGGGAAAATTCT	154214
rs562734816	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124997315	ACATGTTGTATTACA[A/G]TCCTGGTGCTTAAGT	154214
rs562765511	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989428	CAAGAGTCATGGTAA[A/G]GTAATATGCATGGCA	154214
rs562772438	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989985	TTGCAAAAGTTGTCT[C/T]CACTCCCATCTCTTA	154214
rs562783016	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125031231	CCTCCAGGCCTGTGA[C/T]GCTAGGAGCTGCGAT	154214
rs562783525	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962396	CGGGCTCCCCGGAGG[A/G]GACTTGGGGCGTCCC	154214
rs562854102	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998260	CCATGGATTCACCTT[G/T]TATGTCATTTACATT	154214
rs562871857	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025909	GAAGTTTTTGACTGT[G/T]TGCATATTGGTCAGT	154214
rs562915381	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125061397	TATTTTATATTTTCC[C/T]GTTTGCTTGTAAACT	154214
rs562932992	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018994	AACTTGAGGATTCTT[C/T]TCTGGGGAAAGTGTA	154214
rs562943695	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124998612	AGACCATCCTGGCCA[A/G]CATGATGAAACCCCA	154214
rs562991663	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005608	AATCTTTTGAAAGAA[A/C]TTTTTTCTTAAATCC	154214
rs562996360	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125019835	CCCTTTTTTGCAGTG[G/T]GGGGGGAGTGAAAAA	154214
rs562997583	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066446	CTGCTGGCTGTGCTT[C/T]GAAACTGCAGGTATT	154214
rs563011369	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125060288	ATTATCACATATTTT[A/C]ATATAAATGCTTTCA	154214
rs563052018	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961571	AAATTAGTTATCAAC[C/T]CTTCTAAGGATTCCA	154214
rs563113690	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025724	AGTGGGGAACAGAAA[A/G]TTGAAGGTGTTCTAG	154214
rs563164996	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046852	TCTCATAGTTAATTT[A/C]TTTACTGTTTTTATG	154214
rs563210688	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125021426	GCCTGCCACCATGCC[C/T]GACTAATTTTTTGTA	154214
rs563212036	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033349	TCCCTCCCCCCTCCC[C/T]CCACCCCACAACAGT	154214
rs563252323	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964551	CATGTGATTCCTCTA[C/T]GTTTTTTGGCTAACT	154214
rs563269780	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014308	GTTTGTACTGCTCTA[A/C]ATTCCAGGCTGTACT	154214
rs563270245	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124996208	TAAGTGTTTTGCCAG[A/T]CTGCAGGGTATGAAT	154214
rs563367110	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125051923	GAAGAAATGGGTCCT[C/T]GGACAAGAAATAGAC	154214
rs563388525	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125074854	ACAACTACTGAAGGA[C/T]TTGACACACTTGTTA	154214
rs563430732	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125048860	TGGCAAAAATCTGAG[G/T]AAATAGAGCTTTATA	154214
rs563435352	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125034330	TTTTATGGTTTTAGG[C/T]CTAACATTTAAGTCT	154214
rs563457866	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985216	ACTGTTTGTTCCCAG[A/G]AAAACTCCTGCACTT	154214
rs563509239	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055497	TCAGCACTTAATCAC[A/C]AAGATCTTTGAGTCA	154214
rs563513965	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069344	ATTCATTTGGAGTTT[A/T]ACACCTGATAATTAC	154214
rs563519764	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124970583	TGAGTAGGCAGTTGG[C/T]GTCTGGCATTCAGAA	154214
rs563552390	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042274	TTGTCAACAATGATT[C/G]CAATTCTGTAGGTCT	154214
rs563586516	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090053	TTTAAGTGTCATATG[A/G]CAACTCCTCAATAGC	154214
rs563603014	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999315	AAGCTGGCAGGGATT[C/G]ATTTCTTCCTTAGCT	154214
rs563612954	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125081106	TTAGCATTGCGAACA[C/T]TGAAAATGGAAAGGA	154214
rs563627927	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124963935	CTTGGCCTTTGCCTA[C/T]TTTTCAGTTTCCTTT	154214
rs563632749	in-del	-/TTC	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125007226	GCCTAATGGTTTCTA[-/TTC]TTCTTTTTTTCACTT	154214
rs563666355	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125030252	GAGATTTCAGTGGGG[A/G]CACAGCCAAACCATA	154214
rs563680198	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125051479	TCCATATTTACTTAC[G/T]TAGATTTGTAAGAGA	154214
rs563703213	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125032161	TTCTGAGAAATACAA[A/T]TCAAGTTGAGATTTG	154214
rs563715979	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070609	TAGTGATGCTGAGCA[C/T]TTTTTCATATGTTTG	154214
rs563776575	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064618	ATGAAGAAGTAAAAG[A/C]GGAAATGAAGAAATA	154214
rs563806040	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029479	AAAACTCCAGGTAAT[A/G]AACAGACCATTCGTA	154214
rs563810333	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976626	TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA	154214
rs563819090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000023	TACTGATTACTGCCA[C/T]TGGTCTTGTAATGAT	154214
rs563821619	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965639	TGAGTCATAGATACC[G/T]GGCATGCTTTCACCT	154214
rs563829783	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124968922	AACAAACATTTATTG[G/T]GGTACCTGTATGATA	154214
rs563848461	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968169	TTGAATGCAGTTGTC[C/T]TCACACAGGTGAATT	154214
rs563865929	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092577	ACCACATGATGTGTG[C/T]AATACATCATGCAAT	154214
rs563866580	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000778	GTCTAGCAGTGTGCC[A/G]TATTACTGGAAGGGG	154214
rs563868486	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124965449	ATGGTGGCGCATGCC[A/T]GTAATCCCAGCTACT	154214
rs563870242	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124993178	ACTTACTATCAGAAA[C/T]GCATGAGGCATCTAT	154214
rs563985616	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125035777	GAAGCTTTTTCATTC[A/G]CCTTTTATATTTACA	154214
rs564017044	in-del	-/TATTATT	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125036900	ATTATATTTATTATA[-/TATTATT]TATTATTTATTATAA	154214
rs564019720	in-del	-/AAT			intron-variant	RNF217	GRCh38.p7	6:124984546	ACCCTTTCTCAAAAA[-/AAT]AAAAAAAAAAAAAAA	154214
rs564024233	snp	C/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125077347	GTGATAAGTTGCATA[C/T]ATTTTTCATTGTTTT	154214
rs564027979	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057222	TCTCTGTCGCCCATG[A/C]TGGAGTGCAGTGGCA	154214
rs564048867	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125029933	TGTTACTCCGTTTTC[A/C]TGCTGCTGACAAAGA	154214
rs564054652	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008496	AGTTTGAATATCCCA[C/G]TCATCAGCACAGTCC	154214
rs564076495	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022746	TACTTACAATTACAC[A/G]TTACACGCTAGACAA	154214
rs564133211	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086588	ACATTAGATTATGTA[C/T]GATTTAGTGATTTGG	154214
rs564135426	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988070	TGAGCTCCGCCTCCT[A/G]TCAGGTCAGCGAAGG	154214
rs564176005	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124988788	GTTATTCCACAGAGA[A/G]TGTTCATTCATAGAG	154214
rs564222721	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050669	ATATAAGAATGTGTA[A/G]AGCTTTCCCATGAAC	154214
rs564239092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002643	GTGTCACGCTGGCCC[C/T]GTATGTTCCTGTTTG	154214
rs564250541	in-del	-/GTG	0.00398564	0.0444627	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965138	GAGGGACATAGTCAA[-/GTG]GTCATTGCAGTGTAC	154214
rs564281139	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125044887	CATCATCTGAATGCT[G/T]TCTAACCCTGCAGTT	154214
rs564320885	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036016	TGCACCCATCAACCC[A/G]TCATCTAGGCTTTAA	154214
rs564365433	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052496	TGCCTCATGAAGACT[A/G]TATGTTACTGGCATT	154214
rs564424046	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044003	CAACTTCTTAACTAC[C/G]TTACCTCAAGTTTGT	154214
rs564434674	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036525	AAGTTGACAAATGGG[A/G]TCTAATTAAACTAAA	154214
rs564435476	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079406	TATATAAACAAAAAC[A/T]ATGGAGCCTTCTCCA	154214
rs564461982	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031092	CTGAAGCCACAGCCC[A/G]AGCTGTATGTTGGCC	154214
rs564530038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025146	AGATGTTGCAAAGGA[A/G]GCAGTAAAGTAAGGA	154214
rs564530586	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012042	ATATATACTGAATCT[A/C]ATTAAAAGCCTTAGA	154214
rs564554459	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078589	TGTCAGGAACCCACT[C/G]CCTTGATAACTAACA	154214
rs564564698	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125033043	CATTTTCATATGCTC[A/G]CTGGCCATTTGGACA	154214
rs564628061	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124981115	ACAGACACTATATGG[G/T]GCTTAAGAATACTGT	154214
rs564645017	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024518	AGCTCAGGAGTTCGA[A/G]ACCACCCTGAGCAAC	154214
rs564712210	in-del	-/ATATGTATGATGTATATATGTC	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085006	ACCTAGCTGATCTGT[-/ATATGTATGATGTATATATGTC]ATATGTATGATGTAT	154214
rs564713796	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967060	ATGAATCTTTAGCAC[A/C]ACAGTATATGTTGAT	154214
rs564752563	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967882	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCTTCAG	154214
rs564761517	snp	C/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125039199	TCCTTTTTATGGCTG[C/G]ATAGTATTCCATGGT	154214
rs564764276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052830	GGTTAGTTTCTTTAG[A/G]ACATACCCGAATCTG	154214
rs564771062	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059095	AATAATAATAAATGT[A/G]CAGATTTACTATACC	154214
rs564782659	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004582	GTAGGTACAGAAGTG[A/T]TCTAAGTTGGGATAG	154214
rs564786928	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044538	GAATACATTAATTTT[A/G]TAAATTACCGCAGTA	154214
rs564821279	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032768	AATTTAAAAATTTGC[A/T]TAAGAGGATAAGGGA	154214
rs564831017	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124972901	TGTATTTAAATTGTC[C/T]GTTTCCTGCTCTGTG	154214
rs564833091	snp	A/C/G	0.00319098	0.0398384	intron-variant	RNF217	GRCh38.p7	6:125059992	TTTATGATGTGTTTG[A/C/G]AGTATAAATGGTTTC	154214
rs564870609	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052155	ATAAAAGCTAGTATT[C/G]AGGTGAATGCATTGT	154214
rs564877348	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125020637	GTAAACATCTGTTCC[A/G]GGTAGGATTCTAGAT	154214
rs564883265	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961209	TGTAAATTGAATTCC[C/G/T]TCTCAGGAGAAAAAA	154214
rs564953380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076276	ATCTCTGCTTATTCC[C/T]CCAAGTTGGCTCATT	154214
rs564963054	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124996712	GATGCAAAAGTAAAT[G/T]ATTACAATGAGACTA	154214
rs565024499	snp	A/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962576	GCACGGTGAGCGGCG[A/G]CGGCGGGCCCCAGGA	154214
rs565070339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990104	ACAATTTATCACTCT[A/G]TCCTCCTTGAAATAC	154214
rs565082710	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125080448	GTTTCTTTTTTAGTG[C/T]AATTGATTATTCTAA	154214
rs565083501	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058109	TCCAAAGTGCAAGGT[A/G]AGATAACTTTTAGGA	154214
rs565091399	in-del	-/G	0.375996	0.215928	intron-variant	RNF217	GRCh38.p7	6:124984555	CAAAAAAAAAAAAAA[-/G]AAAAAAGAAAGAAAG	154214
rs565097016	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125064018	CAAAAGCTATTTTTT[C/T]GGTCTTTTATATCTG	154214
rs565109682	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124990513	AGTTTTCACCATTTC[A/G]GTTGATGGCCATTCC	154214
rs565124107	in-del	-/TT	0.329112	0.237152	intron-variant	RNF217	GRCh38.p7	6:125004065	AATGAGGGGTTACAG[-/TT]TTTTTCTTTAAAATT	154214
rs565143509	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019931	GCTGTTTGCCTCTTA[C/G]CTTAGTCAGCTTTGT	154214
rs565157313	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125049961	AGAAAACATGACTCA[C/G]GAGTGATTTGGTGGA	154214
rs565185025	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125037947	ATTTGATAAATTGAG[C/G]AATGAGGCCTGAGAT	154214
rs565203186	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090306	TGAGAGATGACAGAA[A/G]TGATTTTCTGTAGAA	154214
rs565206109	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976274	CTCCCTCCCTCCCTC[C/T]CGCTCTCTCTCCTTT	154214
rs565264250	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082306	GGGTTTTTTTGCTAA[A/C]TAAAATGATTTTCGT	154214
rs565301331	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989765	GGTTAGATGTGGCCC[A/G]TGGACCAAATAATTT	154214
rs565302292	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054675	TTTTGGCTTAGGGAC[A/T]CATTCCTGGTCCAAT	154214
rs565303052	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053382	GAAAATGAATTGATA[C/T]ATGTGCTTCATTATT	154214
rs565346525	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020658	GATTCTAGATAAAGG[A/C/T]GTATTGCTTTGGCTT	154214
rs565410202	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125005755	TATTAGATAAAACTG[C/T]ATGCAATAGAAAGCT	154214
rs565419971	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125013402	GTGCTGTTTTTGAGA[C/G]CATGGTCGTGGAACG	154214
rs565424637	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085749	CACTGTTAATGGTTT[G/T]GTATGTGTCCTTCCA	154214
rs565446610	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991443	AACCCTCATCCCCCC[C/G]ATACCAGCATTCTTC	154214
rs565559003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020335	ATATGATCCAGAGAA[A/G]GAGGGCTTGAGACAA	154214
rs565570855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995644	AAACATTTGGAGGGC[A/G]GGTGCTGTGGCTCAT	154214
rs565571460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047825	GTTAAGATCCTCAGC[A/G]GTGGGTGTGGGGTGG	154214
rs565579817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999195	AGACTGGCTGATCTT[C/T]GGTATATTTCATTTT	154214
rs565590642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125043561	AAGAGGAAACATTTA[A/G]TCATTTTTTAATGTT	154214
rs565645123	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040449	TTGAGGCAGTAATTA[A/T]TAGCCTACCACCCAA	154214
rs565689209	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027390	TTAGATCCCAGAAAT[A/T]AGTGAGAACATGCAA	154214
rs565747135	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125018407	AATGATCTCATTTTA[C/T]TTAAGGGACAGTTCT	154214
rs565750258	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021004	GGAACGTAAATAAAC[A/G]TGGCTTTTAGAAAGC	154214
rs565770405	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125034693	GGCTCTTTTTTGGTT[C/T]CATATGAACTTTAAA	154214
rs565789985	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999003	TTCAAAAATAGATAC[A/G]TGTAATTATACCTTT	154214
rs565803596	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962895	GGAAGCTGGGGATCG[A/G]AAAGAGGGAGGGGAT	154214
rs565829730	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035172	ACTTCCTCTTTTCCT[A/G]GTTGAATACCCTTTA	154214
rs565831654	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028710	ATTATTCTCTTTTTA[A/C]ACTTGTACCTGTGTT	154214
rs565840551	snp	C/T	0.00265604	0.0363451	intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963448	TCACCCCCTTCTCTT[C/T]CCCATTTATCATTCC	154214
rs565841609	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021341	GCGCGATCTTGGCTC[A/G]CTGCAACCTGTACCT	154214
rs565852051	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124986364	GGAGGGCAACCATCA[A/G]GCAACAGACTTCCTT	154214
rs565862221	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054965	GTGGGTATGTGGTTG[C/T]GAGATAGCATTTCAT	154214
rs565876139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991909	CTTTTCTGTCATACC[A/G]GAAAGCTCTATTAGA	154214
rs565886473	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125016194	AGAGGCATATGGTTC[G/T]TTCATTATTCTTTGT	154214
rs565892462	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125029570	TTCTGTTAAAGAACT[A/G]TGTTAACTTGGTTTA	154214
rs565955729	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090613	TATTCTCCTTAACAA[C/T]AGAAAATTAGAAGAA	154214
rs565971382	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124979651	AAGAGATGACTTACA[A/C]AGGTAATAGGGTCAG	154214
rs565971787	snp	C/T	0.00017727	0.00941296	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048239	ACTGAGACTAAGATC[C/T]TTGTTCTTTGTGATG	154214
rs566007032	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999473	CTTTTTTTTTTCAAG[A/C]TTTAAAATTGTGGTT	154214
rs566015672	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962118	ACAGGCCCCTCGACC[C/T]TTTGACCACCGCCCT	154214
rs566039353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056705	ACATGCTGCAGTGAC[A/G]TGACATAGAGGAGCA	154214
rs566039476	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064732	ATTTAATATTTTAAA[A/G]TGAGGACAAAATAAG	154214
rs566074715	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125026779	TTGACCCTGTGGAAG[A/G]CAAGTGGGGTGTGAA	154214
rs566078918	snp	A/G	1.97748e-05	0.00314436	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082967	CATCCAGCTAAGCTG[A/G]TTGGAGTAGGAGCGA	154214
rs566102263	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021645	AATAAATATATTCTA[A/C]AAGGACTTATATGAA	154214
rs566131253	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971690	TGATCTCTTGACCTG[A/G]TGATCCTCCTGCCTC	154214
rs566138609	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083708	ATTAAATTAAAGTCA[A/G]TGTAGACAACAGGCC	154214
rs566181539	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978483	AGAGATGCCAGCAGT[C/T]GTGGAGCCCCAAGGG	154214
rs566183496	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986915	GCTTGCCTGGGGTTG[A/T]ACATTAATGTTTCCT	154214
rs566191192	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124985354	TTATGGGTTATATGA[C/G]ATGTTTTCATACAGG	154214
rs566240108	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076208	GACCTCTGCTTTTTG[A/G]TATTTATTCACAAAA	154214
rs566285785	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125022161	TGCTGGGATTACAGG[A/C]CTGCACCACCATGCC	154214
rs566291151	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125080901	CTAACATCTTGAAAC[A/G]TCCCATTTTTAGTTC	154214
rs566325219	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125077620	TGCAGGGTTCTTCGG[C/T]GGAATATTTCTTCTT	154214
rs566332942	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125037113	CCACTGCCCTGTAGT[C/G]TTCATATGGAAGTGG	154214
rs566349132	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015569	AATAAACATAAATGC[C/T]AAGTTATGATAGTAT	154214
rs566352369	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078927	TGTTGTAATTTACAA[A/G]GTTACTTACTCCCTG	154214
rs566377461	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965109	GAAGTTTTAGTAATG[A/G]TAGTAGGGAGACAGA	154214
rs566386382	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077981	TACGCAAATGCACTT[C/T]CACATATGGAAACCA	154214
rs566418569	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125001394	GACTTAATTCGAGAA[C/G/T]GGTAGAATGAAGGAA	154214
rs566424095	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125008064	GATCAAGACCATCCC[A/G]GCTGACATGGTGAAA	154214
rs566435368	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980358	TACTTTTTAAAACAA[A/T]TAGGAACTACCTACC	154214
rs566484453	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125008591	TGTGCCCTTGACAAA[A/G]TGCTGATTAGTCCTG	154214
rs566493573	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125049915	GATAGTGTTAAGTTT[A/G]AAGACCCTTTAGGGC	154214
rs566500658	in-del	-/TATATATA			intron-variant	RNF217	GRCh38.p7	6:125071536	GTGTGTGTGTGTGTG[-/TATATATA]TATATCTTATTACAG	154214
rs566505286	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068553	CTACACCTATAAGCT[C/T]CTTAAGGGCAGGAGC	154214
rs566512980	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125034722	AAGTAGTTTTTTCCA[A/G]TTCTGTGAAGAAAGT	154214
rs566521564	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973824	ACCTAGGAACATAAA[A/G]AAAAAGAACGATTTT	154214
rs566535554	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092952	CTCTAGACCAAGGGG[C/T]CTATACAGGGGTGGG	154214
rs566544780	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125001281	TTTTCTCTTGTTACC[A/G]GTTTTTGTGTGTTTG	154214
rs566557319	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124974316	TTAATTTTTTTAAAA[A/T]ATTTTGTCTTTTCAA	154214
rs566570051	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042591	TATATTCTTCGGAAA[C/T]TGAATAGATTTGCAG	154214
rs566614166	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009765	CTGCATTCCATCTCC[A/G]TGCACATTCGTTGGG	154214
rs566642731	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125036119	GTGTGATGTTCCCCT[C/T]CCTGTGTCCGTGTGT	154214
rs566646764	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009101	GCTTTCCTGAACAGA[C/T]GTGTTAGAAATGTAT	154214
rs566670998	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125010840	GCTGAGGAATGATCT[A/G]AGGTCTGCCAGCTCC	154214
rs566684847	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062663	CTCACTGCAACCTTC[A/G]TCTCCCGGGCTCAAG	154214
rs566692022	in-del	-/AT	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125054133	TGGGCTGTTGGAGAG[-/AT]TAGACATCTACATCC	154214
rs566760564	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125048419	GAAATAGAAAAAAAA[A/T]GGTTGCTGCTAATGT	154214
rs566775495	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024622	ACTCGGGAGGCTGAG[A/G]CACGAGAGAATCTCT	154214
rs566778439	in-del	-/A	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091602	GTACTTTAAAACCAT[-/A]AAAAAATGCTAATTA	154214
rs566797092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003822	AAGAAGCTCATAGCT[C/T]CTTATATGCTATGTC	154214
rs566837337	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125017269	TATATTTTTCTTTAT[C/T]GAACAAAAACAGTTA	154214
rs566880483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016858	GATGGGTGCAGCAAA[C/T]GGCCATGGCACGCGT	154214
rs566999892	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025468	ATTCCTGACAAGGCA[C/G]GTGGAAATAATCATC	154214
rs567011021	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125026812	CTGCCCAAATCATCT[C/G]CCTTACTGGATGAAA	154214
rs567070578	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993728	CTGTTTGTCAGGGAG[A/G]GTTTTGTAAGGAATA	154214
rs567091980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996837	TTATATTACTTATCT[A/G]TTTTTTACTATATAA	154214
rs567100913	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052349	TGTTTTGTTTTGTTT[A/T]GTTTTGGTCTGCTGT	154214
rs567106551	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124995958	AAAGAAAAACATTTG[A/G]AATATTTCTGGGTTT	154214
rs567120169	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124980776	GTTGCCCCTCCCTCC[A/G]TACTTTGATTTGTTA	154214
rs567128237	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989782	GGACCAAATAATTTA[A/C]TGAACTCTGTCCTAT	154214
rs567139862	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087098	TCACTCTGGTATGTG[A/G]GAAACATTAGAATTC	154214
rs567145372	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037446	ACTTGATGTACTTAA[A/G]TGTTTTCTTTGTACT	154214
rs567169223	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060540	ACCTTCGCCTCCCAG[A/G]CTCAAGCAATTCTCA	154214
rs567192389	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125013274	TAATGGTTAATATTA[C/G]CAGAAAAACAAAGCT	154214
rs567194512	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:124989191	ACCGTCACTTTACTT[G/T]TAGTTGGCAATATTT	154214
rs567226451	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053214	CCCAGCTTCTATTCT[A/G]GCAGTTACTATATGC	154214
rs567268843	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073375	AAGGGCTTAAGCTTC[A/G]AAGACCTTCACCTGC	154214
rs567277946	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125014442	TGATATCAAGCTCTG[C/T]TTTCCTCTTATTTAA	154214
rs567289515	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125053964	TAGGAATTAGTAATA[C/T]TACCTCAGCCACTAG	154214
rs567331646	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125067403	GCTAGCTGTAGACAT[A/C]TGAAAGAAAAATAAT	154214
rs567332490	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080571	TATTGCATTTGAGTT[A/G/T]TGCGGCCCTGAAGCT	154214
rs567374488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969191	GTTATAAATCTATTA[C/T]TTATTTCTTAATATA	154214
rs567377229	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066573	TTTGAGGAAAATTCA[C/G]CTTCTCAGTAAAACT	154214
rs567427434	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124986344	GTTTTGTGGTTAGAA[C/G]AAAGGGAGGGCAACC	154214
rs567448554	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968273	TTTTGAGGTCACTCT[A/G]AAAATTTGAAAAGTG	154214
rs567514750	snp	C/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125082347	GGGTTTAGCAAGTAA[C/T]AAATGTGCAGGACAG	154214
rs567518567	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074423	TACTATGATTAATGG[C/T]CGTTATTAGTTCACA	154214
rs567584338	snp	C/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124977325	TGCATACTTGTGCAT[C/G]TCTTTGCCTGTATGA	154214
rs567599589	snp	G/T	0.00478085	0.0486577	intron-variant	RNF217	GRCh38.p7	6:125013255	CATAACAGGACAGGG[G/T]TGATAATGGTTAATA	154214
rs567601349	snp	C/G/T	0.000138408	0.00831788	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962768	CGAGGAGCCTGGGGC[C/G/T]CCCGGGCTGGAGTAA	154214
rs567621064	snp	A/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124978083	GCTAATCATTATGAT[A/T]AAGATAAACAATGTG	154214
rs567648224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039530	CACATTTTCAATATT[A/G]GACAGATCAACAAGA	154214
rs567691448	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991088	AATGTAAGACCTGAC[A/G]TGTTGCTCTTTTACA	154214
rs567694156	snp	A/C/G	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125007985	TATGTGGCCGGGCCT[A/C/G]GTGGCTCATGCCTGT	154214
rs567698956	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125054880	CCTGCAACCACACTT[G/T]GAGCCACAAGGACAG	154214
rs567705795	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021560	GTGAGCCACTGCACC[C/T]GGCCAGAAAATGCTT	154214
rs567733363	snp	A/G			missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058072	GCGAAATTGAGCATG[A/G]GCAGAGGAATGCCCA	154214
rs567736688	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984090	TTCACCTTTGGTGTT[A/C]CATGAATTTTAGGGA	154214
rs567779230	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090380	TTTTGATTCTATTTT[A/G]AACAAAATTGTAAGG	154214
rs567815001	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033061	GGCCATTTGGACATT[A/G]TCTTTTGTGAAGTAC	154214
rs567865037	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033485	TTACTGAGAATGATG[A/T]TTTCCAATTTCATCC	154214
rs567889152	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068920	GGATTTAGTAGGATG[A/G]CATGTATAATCACAG	154214
rs567905256	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021161	TTTATAATAGCATTA[A/G]GTTGGAGACAGCCTC	154214
rs567911956	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984784	AATATTTCTTAGAAC[A/C]TGAGAAATACAACTC	154214
rs567934124	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125023685	CCTAAGTGCCCATTG[A/T]TAGATGAGTGGATAA	154214
rs567947574	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062769	TTTAGTAGAGACGAG[A/G]TTTCACCACGTTGAC	154214
rs568013435	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124966343	AGACAACCTGTAATA[A/C]CCCACCAGTTCCAAA	154214
rs568066307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021564	GCCACTGCACCCGGC[C/T]AGAAAATGCTTACCT	154214
rs568096445	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063170	AATTCATTTTAGACT[A/G]TTTTATACCACAGAT	154214
rs568111146	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055088	TTCAAAATGAATGAG[G/T]CATCTTCAGAACAAA	154214
rs568125320	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125075940	ATATACCATACCACC[A/G]CTGTATGGTATATAT	154214
rs568163781	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125074114	TCCCAGTTCACCTAA[C/T]GATTTTGAATACATA	154214
rs568166525	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091088	AGCAATCAACTTATT[C/T]CCAAATTATTATTTC	154214
rs568171947	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055610	GACTGATTAAAAACT[A/G]GAGAGATCTTTTCAA	154214
rs568173795	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:125007323	CGATCTCGGCTCACC[A/G]CAACCTCTGCCTCCT	154214
rs568188095	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085516	ATGTCAGTGCCAACT[G/T]TGAAGGTAAAACAGT	154214
rs568189540	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125041065	CTCTCACCACTCCTA[C/T]TAATGATCTTTGTTC	154214
rs568191173	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125022227	CCACAGCAGATCTAT[C/T]TGGTTTATAGGAGAA	154214
rs568195386	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125030034	GAATCATGGCGGGAG[A/G]TGAAAGGCATTTCTT	154214
rs568230400	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083077	TTCTCCGTGGGCCAC[A/G]ATGCCTCTAGCTATG	154214
rs568252958	snp	C/G	0.0107246	0.0724382	intron-variant	RNF217	GRCh38.p7	6:125034894	GTGGTTTGTAGTTCT[C/G]CTTGAAGAGGTCCTT	154214
rs568253987	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023090	GTAAAAATGACAGGA[A/G]TAAGCACAGGTTGCT	154214
rs568275248	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986103	GTCACAAAGGTAGAA[A/T]TGATCTTCTCCATTA	154214
rs568277823	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964133	TTTTTTTCTTGGAAA[A/G]CTTGAGAGTGCACCA	154214
rs568290322	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125049145	CAGTGCAACAGCAAC[C/T]GCTTATCAATATAGA	154214
rs568315362	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092032	TTAGAAAAGACAAAG[A/T]CAGGTTGTATATGCA	154214
rs568337017	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041825	TCCAGAAGTCCATCA[C/T]ACTACCTAGCCCATA	154214
rs568378045	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083954	TATTTAATCCCAAAA[A/G]CAAGTTTGCTGTAGA	154214
rs568391064	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124969300	ATTTTCTGCCTTTAT[A/G]TAAAGAAAACACAAT	154214
rs568397969	snp	C/G	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125035262	GGTGAGAGAGGGCAT[C/G]CCTGTCTTGTGCCAG	154214
rs568421361	in-del	-/GGGTTGTCATGGAGGATATGTTTTACGAA	0.00874735	0.0655527	intron-variant	RNF217	GRCh38.p7	6:124969872	TCTATAGTTTTGGGG[lengthTooLong]GGGATTTTTGAGAAG	154214
rs568465338	snp	A/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124979705	TTATACTTTATTTCA[A/T]CTATGATGGTAAATC	154214
rs568478724	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050364	TTTATACAATGGCAC[C/T]TTTGATGCATCTTTC	154214
rs568485710	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125063982	AATGAATAATCTTCC[C/G]CTGTTCACATAAGGT	154214
rs568527271	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125077425	GTGCATACAAACCCA[A/G]GTTTAATTATCCAAG	154214
rs568533079	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125033822	ACCAACTGTGTAAAA[C/G]TGTTCCTATTTCTCC	154214
rs568539391	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124977481	AATGCTTTCACAATT[A/G]CTGGTGTCAGCAAAA	154214
rs568552644	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124965222	TGCAGCATTTCTGAT[A/T]GTATGTATGTGCCTG	154214
rs568571121	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972245	CACCAGGTCCTTTCA[A/G]TTCTTCATCTTTAAA	154214
rs568610555	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124971454	TACTGTTAAGTTTTT[G/T]TTTGTTTGTTTGTTT	154214
rs568626847	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064775	TATTATTTTTATATG[A/T]ATATCACATGTCATC	154214
rs568639380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016048	ATATAAGGAAGCCCA[C/T]GAATCTAATGACACT	154214
rs568684910	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009407	TAGATTTTTTCACTT[C/T]CCTTGAGTATAAGTG	154214
rs568685949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057403	GCCAGGCTGGGCTTT[A/G]ACTCCTGACCTCAAG	154214
rs568699698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965933	TATCTTTAGCATCTA[C/T]AGCGTTGTCTGGTAT	154214
rs568700750	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125078981	ATAGGAAAGCCCTCC[C/T]ACCCACTGTCCTTGT	154214
rs568747393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973905	CAGTTCACTTTCGGG[A/G]TTTCTCATTTGGTTG	154214
rs568797107	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125001361	TAGTAAATGGAGTTG[C/T]CTTCTCTAAATTTGT	154214
rs568891039	in-del	-/TTCA	0.0209421	0.100162	intron-variant	RNF217	GRCh38.p7	6:125055768	TCCTTCTTTCCTCAT[-/TTCA]TTCATTATATTGGAA	154214
rs568901095	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975437	AATTAATGAATTATT[C/T]ATTCATTCATTGAGA	154214
rs568910558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037221	AGCTCTATGATCAGT[C/T]TTATTTCTGGCAGAA	154214
rs568930317	snp	A/G	0.0138799	0.0821421	intron-variant	RNF217	GRCh38.p7	6:125072737	CAAGAAGACACAGAT[A/G]TACCTTGTGGAGGGA	154214
rs568939291	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968052	CCCAAAGTGCTGGGG[A/G]ATTACAGGCATGAGC	154214
rs568945858	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988250	AGAGTTGTCTTCCAT[A/G]ATACCAGTCCCTAGT	154214
rs568947051	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994818	TGTACACCTGTTACT[G/T]GAGCCTGAATTTTAT	154214
rs568956662	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988959	GTTAATGTTGCTTCC[A/T]AGTTTTGCAGCTCTT	154214
rs568978753	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058718	ATGTGTTGAAAGTTA[A/G]CCAAGCAAACAGCCA	154214
rs569041746	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088552	TCACATACCTTACAA[A/T]ATCCCTATACATATT	154214
rs569041765	snp	C/G	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125051815	AGAACAGGACATCTT[C/G]TTCAAAACAGGATGA	154214
rs569087222	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124970020	TGAGTTTCCAGGAAT[C/T]GCAAGGAGATCTGTG	154214
rs569090413	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125024228	GGTTGAGGGAGAGAG[A/G]AAGCAGAAGAAAAGT	154214
rs569114263	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009934	TTTTTGGTTCATGCT[C/T]GTCGTTTTCTGTTCC	154214
rs569144378	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:125066447	TGCTGGCTGTGCTTC[A/G]AAACTGCAGGTATTC	154214
rs569147937	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066006	ACTCCAGTCTTCCAG[C/T]TGCTCAGGCCAAGAA	154214
rs569212435	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025339	CAGATGATAAGGACT[G/T]GAGACCAAGGCACAC	154214
rs569217351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990189	GGATATTTATTTTAT[A/G]ATTTGTTGTTAATTA	154214
rs569217687	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125011706	ACCTTTAATTTTTTT[A/T]AAAATGATTTACTAG	154214
rs569222894	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005174	ATTAAATTTCAACAT[A/G]AGCTTCAGAGGGGAT	154214
rs569250839	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125063533	GTACTGACATTTATT[G/T]CATGTCAGTCTCCTC	154214
rs569275132	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018123	GTTTTTTATAGAGAC[A/T]TGGTATGAGGGCTCC	154214
rs569279582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004056	CTTTCTTTAAATGAG[A/G]GGTTACAGTTTTTTT	154214
rs569300403	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125003376	GTTTTTGGTATGTGA[A/C]CTTGGAAAAGTTAGT	154214
rs569327950	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125026384	ACTGAGGTTAATCAA[C/T]GGAAAATGCTTAGAA	154214
rs569373252	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052497	GCCTCATGAAGACTG[C/T]ATGTTACTGGCATTT	154214
rs569417453	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088959	TGCAGTCTTCTTCCC[A/T]TCTTGGCCAAGTGTG	154214
rs569437133	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124975483	TTGCCTGGGCAGGAG[G/T]GCAGTGGCTCAATCA	154214
rs569437434	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125053011	CAGGCTACATTAGAA[C/T]ACTTGCTGTTTCCCC	154214
rs569440831	snp	C/T	0.00914312	0.0669923	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088018	GTTACAAAATTCTTT[C/T]TTTTTTTTTTTTTTT	154214
rs569497714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046103	ACAGAGGAGGTGCAG[C/T]TCTCCAGACAGATAA	154214
rs569503198	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032195	GGGGACACAGCCAAA[C/G]CATATCAGCTGCTTT	154214
rs569525073	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031659	ACCACCTCAGCCTGG[A/G]CCTTCTTGTTCATAT	154214
rs569550345	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982844	AAAGTAATTTACTCA[C/T]TTCCTGGTGAGAAGA	154214
rs569569926	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125047481	GAGCGAGCCCATGGT[A/G]TTCTGATAACATTTC	154214
rs569587113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976462	TTTAGTAGAGATGGG[A/G]TTTCACTATGTTGGC	154214
rs569627360	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047114	ACTAGTTTTAGAAGG[A/C]CTCGTAATTCCATAA	154214
rs569647376	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032905	TTAATTGTACAGTTA[C/T]TATTTTAACTGTAAT	154214
rs569656362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073528	TCTGTCATGTAAAAG[A/G]AAAAAAATCACTATG	154214
rs569658768	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021466	GAGACGGGGTTTCAC[C/T]ATCTTGGCCAGGCTG	154214
rs569667842	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124983907	CAAGGCACCAGAAGA[C/T]TCACTGTCTGGTGAG	154214
rs569691671	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052839	CTTTAGGACATACCC[A/G]AATCTGACAGCCATG	154214
rs569720899	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125074313	TAGATAGATAGATAG[A/G]TAGATAGATAGATAG	154214
rs569747164	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125060678	TCAAACTCCTGACCT[C/G]AAGTGGTCCACCCGC	154214
rs569754339	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125013333	AAAAAGAAAGGTAGG[G/T]GCTTGCATGTTTTGT	154214
rs569755284	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977040	CTGTTCATACATGCT[C/T]TTCTCTTTAAAATCA	154214
rs569788262	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969367	TAAAAATGTTTATTT[C/T]TTTCAAATTCAGTTT	154214
rs569799324	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125054164	CCTAATGGAAGTTCC[A/G]TAAGAAAGGTACTGA	154214
rs569803834	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040955	ATCTCAAAATAATAA[C/G]AGCTGTTTATGACAA	154214
rs569817590	snp	C/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125005998	AACTTGGTAATGGGC[C/T]GTTAATTAATTAAAT	154214
rs569825253	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969897	GGAGGATATGTTTTA[A/C]GAAGGGATTTTTGAG	154214
rs569913003	snp	C/T	0.000289866	0.0120353	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962846	TCAATCCCCAGACCT[C/T]GCCACTGCAGTTGGA	154214
rs569961433	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006806	ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGCGT	154214
rs569966714	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125069812	GCATCTGTTGTTTTT[C/T]GACTTTTTAATAATA	154214
rs570010853	snp	A/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124998483	CTATATACATTTTTT[A/T]AATATTGGTCATAAC	154214
rs570034354	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125001858	AAGTGAAAAAATGCA[C/T]AGCAGCTGGAGAACA	154214
rs570088180	in-del	-/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009395	GCCTGGAAGAGTAGA[-/T]TTTTTTCACTTTCCT	154214
rs570109065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027661	TTCCTCTCTTTTGGG[C/T]ATATACCCAGCAGTG	154214
rs570123763	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084459	TTGTCTCCAAATTCT[A/T]AAAATTAGTCATCTG	154214
rs570135171	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991702	TCATTTTTTCTATAT[C/T]TAGAATTGTAAGATT	154214
rs570143815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978143	CTTAGAAACTTTAGA[A/G]CTTTAGTAGGTTAAA	154214
rs570157194	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965076	TTTTCTTTATTAAAC[C/T]TCATAAGTTAGTTTT	154214
rs570173314	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125053865	AAGCCCTGCTTGCCT[C/G]TTTTAGAAGAGTTTG	154214
rs570184760	snp	A/T	0.0111196	0.0737302	intron-variant	RNF217	GRCh38.p7	6:125034604	GTTACTGTAGCCTTG[A/T]AGTATAGTTTGAAGT	154214
rs570206819	in-del	-/CATT			intron-variant	RNF217	GRCh38.p7	6:125028064	GAAAATACTTTCTCC[-/CATT]CATTCTGTGGGTTGT	154214
rs570213661	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050621	GTGCTTAACCTTCCT[C/T]CTGGTAAAGATAACT	154214
rs570246346	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125028372	TTGTAGGTCTTCTTT[G/T]GAGAAATGTCTATTC	154214
rs570253253	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092257	CTGCTGGCGGTAAAA[A/G]CAACCCAAGTGTCAG	154214
rs570262114	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985889	ATGGTTATGTTACAT[G/T]AATCAACTTTTTGGT	154214
rs570267004	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124978383	CTCTGCGCTCAGCCC[A/G]TGGATCAACCAGGCA	154214
rs570313658	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF217	GRCh38.p7	6:125092851	AGAGCACAGAATAGT[A/G]AAGATCAGTGCAAAC	154214
rs570330517	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055719	TTCAGGTGTTCTGAC[C/T]TAATGTTAGATGCAT	154214
rs570357760	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125007403	GGCATGCGCCACCAA[G/T]CCCGGCTAATTTTTT	154214
rs570382362	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987044	TGCCGAATATAGATA[C/T]TAGTCTACTAGCATG	154214
rs570404191	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014891	TGAACTTTTGAGCAA[A/G]CCCAAAGCCCCTTCC	154214
rs570404283	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022128	CCTTAGGTGACCACC[A/T]ACCTTGGCCTCCCAA	154214
rs570465237	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015476	CGCTGAATGGTAGAG[A/G]TTAGTTACATAAATA	154214
rs570631819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125041947	TAAACTATTGTGCAA[C/T]ACTAATTTCTTTTGA	154214
rs570657525	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016802	GGTGGGGGGCAAGGG[A/G]AGGAATAACATTAGG	154214
rs570689738	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084940	TTTCGTAAATTCATC[C/T]TTCCTGAACTTAGGC	154214
rs570696531	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125035367	TCTCGGCAGAAACTC[G/T]ACAAGCCAGAAGAGA	154214
rs570696555	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042494	TTGGTTCAGTGTAGT[A/T]GGATAGGGATTTTGG	154214
rs570717690	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009567	GGTGCCTGGCAGCTG[A/C]CTATTCTATTGCATT	154214
rs570757151	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125036052	GCATGCGATAGTTAT[G/T]TCTCCTAATGCTATC	154214
rs570780152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030521	AATGGGAGCTATTGG[C/T]CAAAAGGCCAAAACA	154214
rs570790327	snp	G/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124980211	ATCTTTTGCGAAGAT[G/T]TCCATAATTATTTCA	154214
rs570821464	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125071071	CCACATTCCAGTTCT[G/T]TTTTTTAGATACTTT	154214
rs570841515	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023857	GGTCCCCCTTTATAT[A/G]TGGAATCTTAAAAAG	154214
rs570844950	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125023139	AAGGATCACCTGATA[C/T]AGTTTTGAGGTATTA	154214
rs570859130	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124970384	ATTGTGAAGTTAGAA[C/T]TGACAGAATGCCAAT	154214
rs570883999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125044372	AAGTAGTTTATTTTA[A/G]TCATTTAAAAATTAG	154214
rs570884145	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024899	ACATGTGGGAGCTTG[A/C/T]ACTGTATATATATGT	154214
rs570912141	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125064809	ACTTGTATGTATATA[C/G]ACATACATATTTATG	154214
rs570956124	in-del	-/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089580	TTGCAAGTGTTTGAC[-/T]TTTTTATTGATATGA	154214
rs570996100	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125002857	GACTCTTGCAGACTT[C/T]ATTAGGCAGAGGAGG	154214
rs570997163	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058491	GCTTTGAATCCTTGC[G/T]ATCTTTTGCTTTTCT	154214
rs571020267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966550	TAAAGAGTTATTAGT[A/G]ACTTTTTTCCACCAT	154214
rs571094243	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002258	GGCTGCTGAGGAATT[C/T]AGCTGCCACTTTCCA	154214
rs571171425	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125054295	AAGCAGAAATGTACT[C/G]TTTCTTGGGCTACCT	154214
rs571191255	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125059441	TTCAAAGCTACTGCT[C/T]AGTTTCAAACAAAAC	154214
rs571266195	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087071	GAGGAGAGACAGGAG[A/G]GGCCTAAAAACTCAC	154214
rs571279927	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124984498	AGGCTGCAGTGCGTT[C/G]TGATCACACCTCCAG	154214
rs571283713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079799	GAAAAGAAACAAAAA[A/G]TTAAGTATAGGAATA	154214
rs571286402	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125060306	ATAAATGCTTTCAAT[C/T]ATGATAACTAAATGT	154214
rs571287241	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079130	ATTCCGTGTAACCAC[A/G]TGCTCAGCTAGAGAT	154214
rs571318993	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031005	GAGGTTTCCAAACCT[C/T]AGTTCTTGACTTCTT	154214
rs571335578	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989074	TTGCTTGTCTAACAA[A/G]TGTGCCATTTGAAAA	154214
rs571338551	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040817	CATTATGTAATCATA[A/G]TCACATAAACAGAAT	154214
rs571344643	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072663	AACTTATTAGAACAA[A/G]TTTTTCTGTCAGGAA	154214
rs571348987	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072195	AATAATGTCTCCTGT[C/T]GCAGATTGCATTTTG	154214
rs571371153	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989617	TATGTTCCAATAAAG[C/T]TTTATTTGTAAACAC	154214
rs571373126	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981468	ATTGGTTTGGTTGGG[A/G]GGGCGGTGACTTTCA	154214
rs571373438	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025441	TGTCTGAAGTTAGCA[C/G]AGGGAGGTGAGATTC	154214
rs571385809	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975607	GGCTAATTATTTTTT[C/G]TTTGTTTTTAGTAGA	154214
rs571391728	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125005399	AAATATGGCTTGCAT[A/G]ACATAAGGGTACAAG	154214
rs571403289	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125071236	GTGAAAGTAACATGC[A/G]TTTGGTAGAAACCAT	154214
rs571406851	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017956	ATCACATTTTCTGAT[A/G]CGTTTAAAATATTTT	154214
rs571445208	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125014699	TTCTGATAGTATGAA[A/T]ACTTCCTTCTCCCAG	154214
rs571474627	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968081	GCCACCGTGCCTGGC[C/T]CCATAAATTCATTTC	154214
rs571499309	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125068227	TACAGATAATTAAAG[A/G]GTTTTAAAATGTAGA	154214
rs571505759	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089776	TGATGTGTTCACTTC[A/G]CCATGCCCCAGCTTG	154214
rs571568261	snp	G/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081639	CTGCTTTAGATAGAT[G/T]ACCAGCATATCATTT	154214
rs571574632	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983060	AAGGAAAAGCTTTCT[A/G]TATATTTCTTCTTCA	154214
rs571576461	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990971	CTACCCGAGAGGGAG[A/G]TGGGAAGATCACATG	154214
rs571594218	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024245	AGCAGAAGAAAAGTC[A/G]GGAGGGGATATTACT	154214
rs571599821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052553	AGGCAGTGAAATATC[A/G]GGGAGTAAGATTAAA	154214
rs571612131	snp	A/G	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124983951	TGCATGGCACCTTCT[A/G]TGCATCCTCACGTGA	154214
rs571614915	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125019308	TACTTATGCTCCTAC[A/G]TTAGAGATTGACTTC	154214
rs571675922	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125012344	AAATTAACATTTACT[C/G]ATGAATTTGAGATAT	154214
rs571699055	in-del	-/AATT			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045628	AGAGTGCTCTTAAGG[-/AATT]AATTACAGTTTTGTC	154214
rs571731297	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125012787	TGATTTGATTTTTGG[C/T]TTTGCTAGCAAATCT	154214
rs571783025	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046925	ATTTTTCTCTTCTAT[A/G]AAAAGCATTATTTTT	154214
rs571792642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125005339	TATTGAGACATCAAA[A/G]GATAAAAAATTCTGT	154214
rs571793173	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:124998351	CTGCTGTGGGATATG[A/G]ACAAGGGGAAGTGAA	154214
rs571807595	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080874	GTACTAGGTATTTAT[C/T]CATAGTTTTCTCTAA	154214
rs571855053	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006210	GTTGGAGATGTTTAT[A/G]TTGCAATAAATGAAG	154214
rs571901742	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125032269	ATTAGTGCAAAGATA[C/T]GGGATAGAAACTGAG	154214
rs571902033	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125039451	CCAGATTCATAAAAC[A/G]AGTTCTTAGAGACCT	154214
rs571953116	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052550	AGTAGGCAGTGAAAT[A/G]TCAGGGAGTAAGATT	154214
rs571955566	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125039832	TAGAAATTGAACAAC[C/G]TGCTCCTGAATGACT	154214
rs571968397	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125019724	GTGCCCTCTGTCTTT[C/T]TCCAACACTTACTGG	154214
rs571997107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124969502	TCTATCAACTTTATC[A/G]CTACTATTTGCCCCA	154214
rs572000350	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125080409	TAGTATGTTTTGACA[A/G]ACTTCCAACAAATGG	154214
rs572018755	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125033208	TGTTCTTTTTTTTTT[C/T]TTATACTTAAGTTTT	154214
rs572026197	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982613	AATCATTGCCGTTTT[A/G]TAGATCATTTATTAA	154214
rs572026398	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124970288	GTTAGAAGACTATGG[-/A]ATAAATCAAAGGAGA	154214
rs572052472	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046555	TCTTTGCAGTAAATG[A/G]AGCAGAAAACCAGTG	154214
rs572061209	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961216	TGAATTCCCTCTCAG[A/G]AGAAAAAAAACAAAA	154214
rs572074951	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997934	CTGTTCTTATGTGAC[A/G]GTGACTCCAAAATTT	154214
rs572079832	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034178	GTAGTTTCTTTTGCT[A/G]TGCAGAAGCTCTTTA	154214
rs572098503	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962110	GCGGCGCCACAGGCC[C/T]CTCGACCCTTTGACC	154214
rs572115063	in-del	-/A	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092072	AAATATTTGACAAAG[-/A]AAAAAAAAGGAAAAG	154214
rs572214814	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089383	GGTATGGTTTATGGT[C/G]TTTGTTTCAGCAAAA	154214
rs572259092	snp	C/T	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124991254	TCAGAACCAGCTTCT[C/T]GGACTCTTTGCTCTT	154214
rs572280396	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981977	AGGTTGCAATGAACC[A/G]AGATCGCGCCGCTGC	154214
rs572281330	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125074585	CTAAAAGCTATACAA[C/T]AAGGTTTTATTTTAA	154214
rs572288371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055398	GTTTGGACACAAAGC[A/G]TCAGATTCTTTATTA	154214
rs572312506	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014436	TATAATTGATATCAA[A/G]CTCTGCTTTCCTCTT	154214
rs572322163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027273	GGGCTTTTTTGTACC[C/T]ATTAACCATCCCTAC	154214
rs572342478	in-del	-/G	0.3742	0.216966	intron-variant	RNF217	GRCh38.p7	6:124984558	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA	154214
rs572344063	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125068604	AGAAAATATTTTTTC[A/T]TGCATTTGGCATAGC	154214
rs572346275	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081822	AATAGAACCCAAATT[G/T]TCTAATTCTGAGTTC	154214
rs572349107	snp	A/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125055746	GCATAAGGAAAAGCA[A/T]TTTTTTTCCTTCTTT	154214
rs572384427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020659	ATTCTAGATAAAGGC[A/G]TATTGCTTTGGCTTG	154214
rs572445862	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971915	CTTTGTATACTGTTA[G/T]TGGGGCCATCTTACC	154214
rs572451847	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984881	TAAACTGAGACAAAA[G/T]ACAATTCACATCTGG	154214
rs572480740	in-del	-/AG			intron-variant	RNF217	GRCh38.p7	6:124976016	CCTAAAATTAAAGAA[-/AG]AAGTATATTCCATGT	154214
rs572503763	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124971125	AAAATCTCAAAGCAA[A/G]GGAATGGCAAAGGTG	154214
rs572512961	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083345	TTAATAGCTGAAGTC[C/T]TATCTGTACCAACAA	154214
rs572547620	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124991585	CCATGAGGATAAGAA[G/T]TTTGTTTGGTTTTGT	154214
rs572554073	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124986452	CTAATGCATGGCTTC[C/T]ATCTGATCCCTTCCT	154214
rs572583756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022371	TTTGAAAATTAACAC[A/G]TTAACAAAAATAAGT	154214
rs572587793	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124963774	GGTATCCCAGAAACT[A/G]ACAAGCAGTGGGCAT	154214
rs572638957	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014129	CCTCAGGTAGCACCA[A/T]TTACATTGTTTTCCC	154214
rs572640418	snp	A/G	0.0023933	0.0345097	intron-variant	RNF217	GRCh38.p7	6:124978808	AGAGGAATAAGGTAC[A/G]TGGACACATGGACAC	154214
rs572640569	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987082	ATTCATAATTTGGAC[G/T]TTTTTTATACGATTC	154214
rs572677338	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124979367	TGGGCAGCTCTCTAA[A/G]TGAGCAAGCATGTGG	154214
rs572702403	snp	G/T	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:125014919	TCCTAATAAACCATG[G/T]TGACCCTGCTCAAAA	154214
rs572704571	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125048635	GTTTGAAAATATTAT[A/G]GCTATTTTATAGCTG	154214
rs572762315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125007524	AGTGCTGGGATTACA[A/G]GCATGAGCCACTGCT	154214
rs572766082	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125041404	GCATGTCAGTCCTCC[C/T]CATAAAACCAGTGAT	154214
rs572806647	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007516	CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG	154214
rs572810577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992934	ATTTAGATATCAGAA[A/G]AAGACATTGCCATGA	154214
rs572825187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076537	TTCACAGCCTCAGGA[A/G]TGCTGTGAGAGACTT	154214
rs572840490	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008403	CTGTACTTAGAAAGA[A/C]GTTAAGCATTAACCA	154214
rs572905308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125035010	GTTTGTCTGTTATTG[A/G]TGTATAAGAATGCTT	154214
rs572924693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125009035	TTTATACCTCATTAC[A/G]TATAATTTTATATCA	154214
rs572966495	snp	G/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125035501	ACAGACTATTTTTCT[G/T]ATGGGTTTGTTGTCT	154214
rs572972644	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124971206	TTTAAATTGATTATT[C/T]CATTTATAAGGTAAA	154214
rs572993351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070551	TTCTTGTAGGAGTAA[A/G]GTGGTATCTCATTGT	154214
rs573009662	snp	A/C	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:125022510	TGCCCTTTTTCTTTC[A/C]ATTAGCACATTGAGT	154214
rs573012222	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125071043	AGGTAGAACCTTGTT[A/T]GAAAATAAAAGGCCA	154214
rs573040115	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065933	CTTCTCCAACGCAGT[A/G]TGTTCTCTTCTCCCC	154214
rs573050162	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002440	GTCGTGCCCCCTGCA[C/T]GCCCCTATCCCCATC	154214
rs573051398	snp	A/G	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125023199	GAGGTAAGACCTGAA[A/G]GATTTAAGCAAGAAA	154214
rs573051849	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059720	GAAGAAAAAGAAGCC[C/G]ACCATGGGGAATTTA	154214
rs573068641	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036407	TGCATGTGTCTTTAT[A/G]GTAGAATGATTTATA	154214
rs573086346	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124994103	AAGTTTAGAAGAAAA[A/T]GGAATTTTAAAATAT	154214
rs573097895	snp	C/T	0.0205511	0.0992634	intron-variant	RNF217	GRCh38.p7	6:124965401	CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA	154214
rs573105611	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125064023	GCTATTTTTTTGGTC[-/T]TTTATATCTGTGGCT	154214
rs573116458	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016365	GTCAATAGATTTTTT[A/T]AAAAGGTGGGATATA	154214
rs573133506	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038790	TCCTATTGTTAGGAG[C/T]TTGGTATGAGTTTTT	154214
rs573143214	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124966057	TAAATTCTATTCTGA[C/G]CTTCTTGATACTTAA	154214
rs573198390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058698	CAATTTGAGCTCAGA[C/T]CTAGATGTGTTGAAA	154214
rs573205390	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125041500	TGCCTAACTCTCCAA[A/C]TTCATCTCATACTGT	154214
rs573212218	snp	G/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088818	TTTTTTTCAGTTCTG[G/T]GCTATATTCTGTCAC	154214
rs573216045	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125055928	ATTTTAATTGTAATG[A/C]TCAAAAAGGAAAACA	154214
rs573230046	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050106	ATGTGTAAAGGATTA[A/T]AAGTAGTTATTTTAC	154214
rs573235035	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125033088	GTACCCATAAAGTCT[C/T]GACTATTTTTCTTTT	154214
rs573291339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042866	TAGGTGAAGAAGGCT[A/G]GATTCAAACACTGAC	154214
rs573370107	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125057425	GACCTCAAGTGATCT[A/C]GCCGCCTCAGCCTCC	154214
rs573408341	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988630	CCTTTTTCTATCCTA[C/T]ATTTTTGCCACCATC	154214
rs573425259	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058850	AAATCTTACTGTAGA[A/G]AATCATGTGTGTGTA	154214
rs573541077	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125052668	AGCAAACAGTGCTTC[A/C]TTGAAAGTATTTGAA	154214
rs573550594	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125078302	AAATCTGTATATGGA[C/G]AGAGCAACATGAAAA	154214
rs573556157	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072340	TTTTTCCGTGATTAT[A/G]TGTATAAAATACTCA	154214
rs573582408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065809	TTAAAAACAGGGCAC[A/G]CATTTAGCTGTTGGC	154214
rs573615410	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079218	CTCTGACATAGGGGC[A/T]TCTCCCCCAGTGAGG	154214
rs573619419	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124980963	GCATGTTGTCTGTAT[G/T]TTAGAAGAACATAAA	154214
rs573632807	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017685	GGGATTAAATTCCTT[A/T]CTTAATTATGTATAT	154214
rs573638336	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991937	AGACAGCCCTGGGCC[C/T]ATGGATTCCCCAAGG	154214
rs573658888	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967795	AAATTTTTTTTTTTC[G/T]TTGAGAGAATCTCCC	154214
rs573677929	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125019123	AATGAGGCTGGCTCA[C/G]AGATCTTCCAGTTAG	154214
rs573693348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011209	ATTTTAACCTTTAGG[A/G]ACAGTAGAAAGCTAA	154214
rs573700874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080205	CACTTTAAGAGTGTA[C/T]TAAACGTAATTATTC	154214
rs573736466	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125008222	GATGGAACCACTGCA[C/G]TCCAGCCTGGGTGAC	154214
rs573744083	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125056909	AAAATATCCTCCATG[C/T]CAAGTGGAAGACAGA	154214
rs573745949	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124967971	TTTTAGTAGAGACGG[G/T]GTTTCACCATGTTGG	154214
rs573761698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073024	TACGCAAAAATTAGC[A/G]CTCTTTCCTTGGTAG	154214
rs573769196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125081162	CTGTCCTGGTAGAAT[A/G]CAGTAAGCCAGTTGC	154214
rs573798627	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125005176	TAAATTTCAACATGA[C/G]CTTCAGAGGGGATGT	154214
rs573806012	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124976099	GTGTATATATGTATA[C/T]ATAGACATATGTATA	154214
rs573810831	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961060	CATTACACTGCTTTC[C/T]TAGTTTGCATCGCTA	154214
rs573821033	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125045025	ATTTCAGAAACATTA[C/T]GTAGTGATTATTTTG	154214
rs573832426	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125073665	CTTGACCACACACTT[A/G]CCTATCTAGGAAAGC	154214
rs573841508	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124996554	CTTTAATCCATTGCA[A/G]TCTGAATTCTGTCCC	154214
rs573842486	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125041661	ATAACAGGCCTTTCA[C/G]TTCTCAACTCAGGTT	154214
rs573873594	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124976642	GTAGCTGGGACTACA[A/G]GTGTGTGCCACCACA	154214
rs573881967	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125003617	TTCATAAACATATAA[C/G]GTGATGGATTTGTTA	154214
rs573892552	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088261	AATCAGAGTTCCAAA[A/C]TTTGGGGAGTATTTT	154214
rs573945057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004152	GGAAATATTAGACAA[A/G]TGTTAAATTATATTA	154214
rs573988685	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089224	CAGAGGGCCTAATAA[C/T]AGTCTAAAACCAAGC	154214
rs573999539	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124970100	GGAGGAGTGGGGAAA[C/G]CTGGTCGGGCAGGGA	154214
rs574029988	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990400	TTGTTTATACATCTA[C/T]GTAATATATCTGCAA	154214
rs574096900	snp	G/T			missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962957	TGGAGCCCAGGACCC[G/T]CGTGGGGGCCGCCGA	154214
rs574108104	snp	A/G	0.00398564	0.0444627	intron-variant	RNF217	GRCh38.p7	6:125031818	TGGTTCCACATTTTC[A/G]GGTATCTTTTCAGCA	154214
rs574114610	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027076	ATGAGCTGTTTTGAT[A/G]TAAGCATGCAGTGTG	154214
rs574122487	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125066260	ATGATGCTGTTAAAC[A/C]TAACGCAGATTACAT	154214
rs574151013	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067709	CTGTGAGGGATATAG[G/T]TATATCTGACTAGCA	154214
rs574155995	snp	A/G	0.00755907	0.0610114	intron-variant	RNF217	GRCh38.p7	6:124998548	CTCAAACCTGTAGTC[A/G]CAACACTTTGGGAGG	154214
rs574212841	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125061302	TAGAAAGTTTGAGGA[C/T]CTGTTTCAGTATGAG	154214
rs574227729	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125012979	TCAGATATAGAATAT[G/T]AAATGTTTATTTCCA	154214
rs574234807	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125051201	CTTCACCTAAAAAAA[-/C]AAACTATAGTAATAA	154214
rs574235033	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068325	GCTGTATTTAGAATT[A/C]TCTCCCTACCTTTAA	154214
rs574236137	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125026545	CATTGAGAGCGTAAA[C/T]GTGTCATCAGTACTC	154214
rs574256026	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962242	GCTGCGGCGCCGCCC[A/C]GAGCTGCATGTGGGG	154214
rs574258643	in-del	-/TGTA			intron-variant	RNF217	GRCh38.p7	6:125052290	CATGCGTTTTGTGTG[-/TGTA]TGTGTGTGTGTGTGT	154214
rs574261077	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125079355	GTATAATTTTTAAGA[A/C]TAGGTCTTCAATTGA	154214
rs574297694	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049571	TGTCACCTTGAGTAT[C/T]GTTTCCACGTCTTTA	154214
rs574298771	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062207	AATTAGTATTCTAAA[C/T]GAAACAAAATTTTAT	154214
rs574315094	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125013498	TAGAGGGGGAGCTTT[C/T]CAGGGAGAAGGTCAA	154214
rs574316408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056025	AGTTTCTCAATTTAT[A/G]TAAGTAGATCTTGAA	154214
rs574346499	in-del	-/C	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125000658	TTAGAGAAATAGAGA[-/C]CCCTAGAATATATTT	154214
rs574377111	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021578	CCAGAAAATGCTTAC[C/T]TTATGTTACATGGAA	154214
rs574429465	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090152	AACCTTATGTTTCAC[A/G]TGAAACATAGAATAA	154214
rs574447923	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021360	CAACCTGTACCTCCC[A/G]GATTCAAGCAATTCT	154214
rs574496100	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124991309	TTAGGACCTTTCCAG[C/T]AGCTGTTCATCTTTC	154214
rs574510640	snp	A/C	0.0115144	0.0749975	intron-variant	RNF217	GRCh38.p7	6:125033285	TGCCATGCTGGTGTG[A/C]TGCACCCATTAACTC	154214
rs574511039	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021721	TTTTCCCCATTTTTC[C/T]GTTTTCCCAGTTTCC	154214
rs574587649	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047621	TTAGTAGAGGAAAAG[A/C]AAATTTGCTTTGGTG	154214
rs574599615	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034271	ATGAAGTCTTTGCCC[A/C]TGCCTATGTCCTGAA	154214
rs574627960	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125082129	CTGCAGTTTCTGACT[C/T]GGTATATGGGAAAAG	154214
rs574649400	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124985141	CTTAAAAGTGCAAGA[C/T]CCAAAAGTCTGGTGT	154214
rs574671487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125069298	TTTATTTTTGCAGCA[C/T]AGTCTACTGTGATAG	154214
rs574678858	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125048720	TAATTTTTGTGAAGA[C/T]CACTTGTTAAATTGT	154214
rs574719367	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091717	TAAAAGTAACTGTAT[A/G]GTACTTCAGGAATTT	154214
rs574729407	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049685	TATGACACATACTGG[A/C]AAGTATTATGATTGT	154214
rs574749594	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125075615	GACCCTGCCCTTGAC[A/G]CGTGGGGATTGTTAC	154214
rs574756954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125014299	AGTTATTGAGTTTGT[A/G]CTGCTCTAAATTCCA	154214
rs574813914	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076361	CTAACCGTTGAATTA[C/G]GTGTATGTCTGGAAA	154214
rs574864530	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089085	TTTACCTTGGCTTAT[C/T]TTATTTGTAAATGGA	154214
rs574894910	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125077312	GAGCCCTGTAATAGA[A/G]TTCCATTATGTCTAT	154214
rs574896902	in-del	-/TTGT	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964392	TTACATGCACTGAAG[-/TTGT]TTCTTTCGTGTCTGC	154214
rs574911503	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086621	GGATAATTATAAATC[A/G]TGGAATAATTTATAT	154214
rs574918002	snp	C/T	0.00159617	0.0282053	intron-variant	RNF217	GRCh38.p7	6:125007654	GGTGACTAATGCTTC[C/T]AACATGTTTTCTTGT	154214
rs574941215	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968032	TGGTCCACCCGCCTC[A/G]CACTCCCAAAGTGCT	154214
rs574951671	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091626	CTAATTAAGTTTAGA[A/G]CAGGAGTTGAAATGA	154214
rs574956811	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125070597	TTCCCTGATAATTAG[C/T]GATGCTGAGCATTTT	154214
rs574967761	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125033631	CCAAGTCTTTGCTAC[-/T]GTGAATAGTGCCGCA	154214
rs575006830	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972564	GTGTCCGTCTGAGCT[G/T]TCTTTCTCAACTGTC	154214
rs575037131	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125028013	TTTGGACTCCTTATA[C/T]ATTCTGGTGATTAAT	154214
rs575042204	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125029612	GGCATTGATACTTGC[C/G]AATTTTGAAAGACCA	154214
rs575057720	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092518	CAAACTATTTTGATG[A/G]TCATTGTACGAGCTA	154214
rs575075952	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124999866	TAAACAGCTATTAAA[C/G]TATTAAATAAATATA	154214
rs575078416	snp	C/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125042188	ATGAAAAAGAGGATA[C/T]TGTTAGTATGAAGAA	154214
rs575120346	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084438	TAAAAAGCCTAAAGC[C/T]TTAAATTGTCTCCAA	154214
rs575129145	snp	A/G	0.00199481	0.0315187	intron-variant	RNF217	GRCh38.p7	6:124966236	ATATTTTTGATCTGT[A/G]TCAATTCTATGGTCC	154214
rs575136282	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085105	ATATACCAACGGGCT[A/G]AATAACATACTCTTT	154214
rs575140910	snp	C/T	0.00318978	0.0398085	intron-variant	RNF217	GRCh38.p7	6:125035732	TACTCTTTCCCAAGG[C/T]CATGAAGATGTTCTT	154214
rs575153170	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124968688	ACAAGTACTGCTGAC[C/G]TAAGGCATCAGCTGA	154214
rs575158637	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125036167	CACTTATGAGTGAGA[A/G]CATGCAGTGTTTGGT	154214
rs575162958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987165	TACTTCCAATTGAAA[A/G]TTAGGTGGAAGCTCC	154214
rs575191409	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125001609	TAAATTTGAATCACA[A/G]TTGTTAAAATTAGGG	154214
rs575221899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124987750	GGAATAGCTGGGACT[A/G]TACCTTGCCTGGCTC	154214
rs575238357	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125030152	CACAAGAATAGCATG[A/G]GAAAGACCAGCCTCC	154214
rs575258183	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993657	CAGTGTAGTAGGTGC[G/T]ACATTAGAGCTAGGT	154214
rs575279860	snp	A/G	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124995688	GCACTTTGGGAGGTC[A/G]AGGTGGGTGGATCAC	154214
rs575293075	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124995259	TAGTTTTAAAAACAA[A/T]AATAAAATGAAAGCT	154214
rs575368151	in-del	-/A			downstream-variant-500B	RNF217	GRCh38.p7	6:125092703	CACAGCAACAAAACT[-/A]ATTGTGCCTACAGTT	154214
rs575369255	in-del	-/TTTGT/TTTGTTTTGT/TTTGTTTTGTTTTGT	0.109973	0.207647	intron-variant	RNF217	GRCh38.p7	6:125052326	GTGTGTGTGGTTTTA[lengthTooLong]TTTGTTTTGTTTTGT	154214
rs575380236	snp	G/T	0.00557542	0.0525036	intron-variant	RNF217	GRCh38.p7	6:124995971	TGGAATATTTCTGGG[G/T]TTTTTTTTTCTATTT	154214
rs575385671	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125065052	AGGCCGAGGCGGGCG[G/T]ATCACGAGGTCAGGA	154214
rs575402431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125022663	CAGTGATCAAGGCCA[A/G]TTTGGCTGTCATCTC	154214
rs575404439	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125013189	CAAAATGAGTCCCTG[G/T]TTTTTGGAGATTATA	154214
rs575412000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016511	TTTTTAATGGAATCT[A/G]TGCAGAAAAGTATTA	154214
rs575446807	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057772	CTTGCCAAAGCAATT[A/C]TTTCCTGTAGTAACA	154214
rs575462696	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058305	CTTATTTTTGCATTA[C/G]TCTTCAAAATTTAAG	154214
rs575489835	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125009875	TAAAAATGTTCAGAT[C/T]CCCATATTGCTTCAG	154214
rs575522995	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125025086	CAGGAAAATCAGGAA[A/T]GTGATGTGCTAGAGG	154214
rs575525204	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125063565	GTAGTTACTATAAAT[A/G]TATTGTCTCATCCAA	154214
rs575530047	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125082599	ATGATATGACTGTGG[A/G]CAATAAAGAAGATTT	154214
rs575553595	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002606	AGCCACCCCGTTTTC[C/T]TCTTCTTGCTTTTAA	154214
rs575561603	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125035959	ACATGTGCAGAATGT[G/T]CAGGATTGTTACATA	154214
rs575590093	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125016872	ACGGCCATGGCACGC[A/G]TATACCTATCCAACA	154214
rs575603884	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065448	CAATTCTGTATTGTG[C/T]AGGATATTCTAAGCA	154214
rs575649916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125018599	GAAAAAAAAGGATAG[A/G]TGGATAAACTGACTT	154214
rs575686552	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087161	GCCAAGACATCAGTC[C/T]AGCTTCTCCCTTGTT	154214
rs575696059	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125050645	GATAACTTGAGAACT[C/G]TTTCCCATATATAAG	154214
rs575717097	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084874	TATCTTAGGTGTAAT[A/T]GTATTTAAGACTGAA	154214
rs575723003	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037533	ATCATTTTTAGAAAA[A/T]TTCAAAGGCATCTAG	154214
rs575738286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124988708	GTGTTTTCTCAATTT[A/G]TTTAATCTTTAAACT	154214
rs575755767	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125079342	TTTAAATCAAGTCGT[A/G]TAATTTTTAAGAATA	154214
rs575777195	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124981087	ATTTTCAAATTAGAT[A/G]GTGTGAGCAGTCACA	154214
rs575783855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031047	GCGGAACACCACATG[A/G]AAGCTGTCAAGGTTT	154214
rs575800306	snp	C/T	0.00676609	0.0577691	intron-variant	RNF217	GRCh38.p7	6:125065163	GGACGTAGTGGCAGT[C/T]GCTTGTAGTCCCAGC	154214
rs575805502	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125027825	GTATTTGTTATTGCC[C/T]GTCTTTTGGATACAA	154214
rs575880892	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125046488	GCCCACCCCAGAACA[A/G]TTGTCTTCCAAATTT	154214
rs575881318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125038380	ATATGGTATCATGGT[C/T]ATGGTTTTAAAAAGA	154214
rs575973886	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125072450	AATATTATTTGACCA[A/G]CGGTATTTTAGTTGC	154214
rs576004984	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011297	AATAATAATGGCCAT[C/G]ATTTATTATGTATTT	154214
rs576007115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125059879	ATAGCTGAAAGGAAA[A/G]GAACCATGGAATCAG	154214
rs576033989	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072776	ATGTTTGTCTGACTG[C/G]TTGGCAAATAATATG	154214
rs576037034	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125011961	TCCCCACCAGGAGGG[C/G]CTGGCCAGATGCATC	154214
rs576091858	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125072738	AAGAAGACACAGATA[C/T]ACCTTGTGGAGGGAG	154214
rs576094235	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125067810	AATAAAGTTGAAACC[A/T]TTCGAATGTGGAAGT	154214
rs576097271	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066732	ATTTTGCAGCTGTGA[C/G]AGCAGAGATTTGATC	154214
rs576099627	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125004481	AGCAGAACAGTGAAG[A/T]TCCTAGCCCTGGGGA	154214
rs576114877	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970189	CAACAGACTAACCAG[A/G]TATGCCTTTCCCTTT	154214
rs576171877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125053451	TTTGGAAAACTGAAT[C/T]AGCTCTTATATTTGC	154214
rs576190454	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125005235	TTTATAACTACTATG[A/G]AAAGGACTGATGTAA	154214
rs576200373	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088405	TCATAGCCAAACTTT[C/G]TGTGGGACTTCTATT	154214
rs576221501	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125068956	AGAGGTGAAGATGAA[G/T]CTGAAGGAGGGGAAA	154214
rs576233968	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089286	CAATATTGTGTTTGC[A/G]TATTAGTTGGACAGA	154214
rs576266425	snp	A/C	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124970830	AAGAAGAGTACTGAG[A/C]GTACTTACCCAGAAG	154214
rs576340063	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124983487	GTCCTCACTTGTCAC[C/T]AATGAAAAGGACCTT	154214
rs576351947	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, splice-acceptor-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963702	CTTATTTCTTATACA[A/G]GATTGCAAGCACAAG	154214
rs576361065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990004	TCCCATCTCTTATTT[C/T]CTTTCTTTCCATTTT	154214
rs576362533	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962094	CCTGGTGCGCGCCGC[A/G]GCGGCGCCACAGGCC	154214
rs576362891	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997918	CTTGAACTGTCCTTA[C/G]CTGTTCTTATGTGAC	154214
rs576429038	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125029198	TTTGGACACCTCTCT[-/A]ATCCAGTAATATTTT	154214
rs576429317	snp	C/T	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124976703	AGAGATGGGGTTTCA[C/T]CATGTTGACCAGGCT	154214
rs576441117	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081571	GAGAGAATACGAGTG[C/T]AAATGTAATAATATG	154214
rs576450942	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990461	CATCTCAAAAACTCA[A/G]TTCTTTTATATTTCC	154214
rs576452190	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124984114	TTAGGGAGAAGCAAA[C/T]ATTCACACCACAGCA	154214
rs576477143	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125027134	ATCCATCCCCTCAAG[C/T]ATTTATCCTTTGAGT	154214
rs576487350	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124977563	GGGAGCATTTAGATT[G/T]CTCTGTTCTAATATG	154214
rs576544644	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125035562	TATGTTCTGGATATA[A/C]AAAACTTGTCATTCA	154214
rs576567587	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125079256	AGATTATTAAAGGAA[C/T]GGTACTGGGAATAAA	154214
rs576570190	in-del	-/T	0.00358779	0.0422022	intron-variant	RNF217	GRCh38.p7	6:124997099	AGAATTTATTTTCTG[-/T]TTTGGTCCGGTGTGT	154214
rs576573579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124992821	TAGTAAATGTAATAA[A/G]TTTACTTTAAATAAA	154214
rs576575555	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124985220	TTTGTTCCCAGAAAA[A/C]CTCCTGCACTTGTGT	154214
rs576593134	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125071321	GCAGCGAGCTGTGCA[G/T]CTGGCAGTCACCCGT	154214
rs576608119	snp	C/G	0.00441056	0.0467528	intron-variant	RNF217	GRCh38.p7	6:125019836	CCTTTTTTGCAGTGG[C/G]GGGGGAGTGAAAAAA	154214
rs576628558	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125076343	AGCATTTTAAATTGC[C/T]TCCTAACCGTTGAAT	154214
rs576631131	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125062795	TTGACCAGCTTATCT[C/T]GAACTCCTGATCTCA	154214
rs576668033	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125020576	TGCCTTTTTTTTTTT[A/T]AATTGCCCTGCTTTC	154214
rs576688593	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995093	TTGTACCCTTGAGTA[A/G]GGAGATGTTTGTGGT	154214
rs576689132	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125055264	AACTTATTTGTATTC[A/T]CTTGAGAGACTGCCC	154214
rs576694352	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124998627	ACATGATGAAACCCC[A/G]TCTCTAACTAAAAAT	154214
rs576722031	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125021792	TTACTTTCCCTGTAT[A/T]ACTGAAAAATTGACT	154214
rs576783507	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015150	TTTTATCTGAAAGTC[A/G]CCTAAAATAGTTGAT	154214
rs576791275	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124999134	AAAACATACTGTGTA[C/T]TATACTGAAGACAAA	154214
rs576792197	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125014069	CTGGATTTCATTCAG[A/G]GCTAGTGTGTACACA	154214
rs576828698	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047359	CTCATTTCATCTGAA[A/G]TCACCAAAATCATGT	154214
rs576849221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125015654	ATATATATTGGTATT[A/G]CTACATCCAGTATAT	154214
rs576877373	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125034345	TCTAACATTTAAGTC[G/T]TTCATTCATCTTGAA	154214
rs576893264	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125047786	GAGGAATTCAACAAC[A/G]CCATAAATGTTGATT	154214
rs576943537	snp	C/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125034947	CCTAAATATTTTATT[C/G]TCTTTGAAGCAATTG	154214
rs576960557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125040641	GATACAACAAAAAAA[A/G]AAAACTTCAGGCCAA	154214
rs576972878	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125076427	ATATTGGTCAAGATA[A/G]GCCAACAGCTTGAGT	154214
rs577007032	snp	G/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125042285	GATTCCAATTCTGTA[G/T]GTCTTGAGTGGGCCA	154214
rs577019808	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011446	GATACGTGTTCAATT[A/G]GGTTTTAGACCCAGC	154214
rs577086278	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125072046	ATGTTTTAAGGCTTT[A/G]TGTTTTAAAAACAAA	154214
rs577164204	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124972338	ACCATTTCTCTCCTG[C/G]ATTCTTACAAGAGCT	154214
rs577222773	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125056950	AAACTTACACGTGCA[C/T]TGTCATATACCCCTC	154214
rs577249813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125006007	ATGGGCTGTTAATTA[A/G]TTAAATAGTTTTTGA	154214
rs577250507	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125008291	GAATGTGGTCTCTCT[C/T]AAAATATCTTACAGT	154214
rs577284125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125057481	GCCACCACACCCAGA[C/T]TGCTACTGTGTTTTT	154214
rs577288919	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125049736	AGCAGAATGAGCAAC[C/T]CTGGGTATTGAGAAG	154214
rs577313261	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125000812	TCCTAAGTGGATAAC[C/T]GTAGTAAAAAGATTT	154214
rs577347608	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124965295	ATACACATTATTGGC[C/T]GGGTGCGGTGGCTCA	154214
rs577377236	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084628	AGTGAAGTTGACTTG[C/T]GTGAATAACAATCCA	154214
rs577408862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125058407	ATAGGAAAAATATAG[C/T]GTAAAAGTGATATAA	154214
rs577408917	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066148	CCCACTATCACTAAC[C/T]TGGGGCAAGGCATCA	154214
rs577454321	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967598	CCAATGAGTATTAAT[A/G]GATACAAGCAACACA	154214
rs577462409	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092605	AATGTTATTTAGCAA[C/T]GCGTAATAAAAGTTT	154214
rs577487088	snp	A/G			missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963293	ACTCTGGCCTGGGCG[A/G]TGTAGGGGATCCCTA	154214
rs577516020	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125026970	TTGTTGAATGAACAT[G/T]ACATAATTTGTACCA	154214
rs577524622	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997812	TCAAAGGCTTTTCTA[C/G]ACTCTACTAACTTAA	154214
rs577530774	snp	C/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124993768	CAGATGAGATCTAAG[C/G]GTAAGTAGGAGTTAG	154214
rs577570241	snp	G/T	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125078136	CGTGCCGCTTCTTAA[G/T]TTGCAAATATGGTGG	154214
rs577585220	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085439	AATGATTATTTGTGA[A/C]TTTTTTACTAAGTTT	154214
rs577590915	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124990640	ACCTTTAAAATATAA[C/T]CAGAATTGAGCCACT	154214
rs577623912	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964532	ACTGAACAGGGCTCC[A/G]TACCATGTGATTCCT	154214
rs577633342	snp	A/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124973432	GTATGTGATAATTTG[A/T]TGTTTATTACCTTGG	154214
rs577658891	snp	A/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:125024351	ACTTTGGGAGGCTGA[A/G]GCAGGCGGATCACCT	154214
rs577669566	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124989323	TAGCAAAATAATCCA[C/T]ACTCCATTGTGCCTT	154214
rs577688174	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088046	TTTTTTGAGACAGAG[G/T]TTCTCTCAATGTTGC	154214
rs577695098	snp	C/G	0.000798403	0.0199641	intron-variant	RNF217	GRCh38.p7	6:124988380	CGACTGCTAACTCAT[C/G]AAATTACTGGCTAAG	154214
rs577758211	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981740	AGTAAAGATCTTGGC[C/T]GAGGGCGGTGACTCA	154214
rs577851616	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124981285	GTGAACACAAAATAT[C/T]TGAGACGGGTTTCAG	154214
rs577853129	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125002716	TGTCCGTGTGATTTT[C/T]GTGCTGGCTTATCAA	154214
rs577890195	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124979184	GACCCTGTCTGCCTA[C/G]AAATTTGTCTGTCTC	154214
rs577931292	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125017625	CTAGGATTATCTGTT[A/C]TATAGGCCTTTAAGC	154214
rs577962823	in-del	-/AGGCCT	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125008512	TCATCAGCACAGTCC[-/AGGCCT]TGGTTTCCAACTTCT	154214
rs577973257	snp	C/T	0.00279162	0.0372561	intron-variant	RNF217	GRCh38.p7	6:124996185	TCAACAGTACTTCAT[C/T]GTATATTTAAGTGTT	154214
rs577987298	snp	A/C	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125011088	GGTGGTATAGGGTAC[A/C]AAGAATGTTAAGAAA	154214
rs578006158	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045569	GGTGAGCATATATTG[A/G]CCATCATTCTGAAAG	154214
rs578012453	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124997137	TGTTAAACTGATGAG[A/G]AGAGAATTTCTGTTT	154214
rs578048593	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125080859	TGAGTAACTTTCAAC[G/T]TACTAGGTATTTATT	154214
rs578060975	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125080119	TGAATGAACAGACTG[A/G]GCTATGTGCATAGGA	154214
rs578091616	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042372	TAGATTCAGCCCTCT[A/G]CAGGGGGAAGACAGA	154214
rs578104648	snp	C/T	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125037587	GAGTAAACAAAAAAC[C/T]GTATGTGTCAGTAGA	154214
rs578108080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125072941	TGAAGAAGAATGCCA[A/G]TCTCATGGTGCAGTT	154214
rs578133376	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044103	TGTTTTTCTTTCCCC[A/G]AACTGCGTGGCTTTC	154214
rs578150910	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125031175	TGCACACACCCTGGG[A/G]ACTGTGGGCCCAGCC	154214
rs578163364	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:124975994	AACACTTTGAAAACA[A/G]TAGGCTCCTAAAATT	154214
rs578186583	snp	A/G	0.00119737	0.0244387	intron-variant	RNF217	GRCh38.p7	6:125018902	GGAGAATCCATATAA[A/G]GGGTGGTAAGTCTCC	154214
rs578239030	snp	A/G	0.000399281	0.0141238	intron-variant	RNF217	GRCh38.p7	6:125066939	ACTTGCAGAAGGGGA[A/G]ACATAGTCCTTAGAC	154214
rs745312103	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011054	CTTTGGAAAGCAATC[A/G]TTTTGAAGGTAGTAT	154214
rs745315080	in-del	-/TCTTTGT	3.47482e-05	0.00416808	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048236	GTACTGAGACTAAGA[-/TCTTTGT]TCTTTGTTCTTTGTG	154214
rs745385149	snp	C/G			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964291	ATCTTTCAAAACCCT[C/G]TGTGTTCAGGTGCCA	154214
rs745417041	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125012058	ATTAAAAGCCTTAGA[C/T]TAAATGAAAGAGATA	154214
rs745439803	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125044174	CCAAGTGCGCATGTT[G/T]TGCTTTCTGAGAATG	154214
rs745447888	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124985695	TATATTGTTCAGAGA[A/C]ATGTGTATAGTATAG	154214
rs745454893	snp	A/C	3.66401e-05	0.00428004	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048176	GCACTGACATGGATA[A/C]CCCAGCCAACCAATC	154214
rs745457759	snp	A/G	1.65285e-05	0.00287471	intron-variant	RNF217	GRCh38.p7	6:125076874	GTGAGTGTCTGACAT[A/G]CTTATGGGTGTCTTC	154214
rs745526666	snp	G/T	4.62097e-05	0.00480653	intron-variant	RNF217	GRCh38.p7	6:125048271	ACAGGTGAACATTTT[G/T]TATTTTGCAGTATTT	154214
rs745541210	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125030764	GCTTTTCCAGGCACA[C/T]GGTGCAAGCTGTCGG	154214
rs745544408	snp	A/G	1.64988e-05	0.00287213	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076737	TTACCGATGTGGTGA[A/G]AGATACCGCCAGCTC	154214
rs745577347	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124986712	CATATTTTAGGTTTT[A/G]TAGGCCAAGAGGCAA	154214
rs745621415	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036950	AGATGGAGAGGAAGT[A/G]GAGAAATAGGAATGC	154214
rs745698601	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990988	GGGAAGATCACATGA[C/T]CCCAGGATTTTGAGG	154214
rs745718325	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968543	TCAAGTGCTAAGCCC[C/T]GGGGCCAGCAGGACT	154214
rs745725428	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022679	TTTGGCTGTCATCTC[C/T]CCCTACCCCATGAAC	154214
rs745782280	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125019831	TGTCCCCTTTTTTGC[-/A]GTGGGGGGGGAGTGA	154214
rs745792468	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125023545	ACTTAAAATAGAACT[G/T]CCAGATGATCCAGAA	154214
rs745816391	snp	C/G	0.000167602	0.00915277	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963120	GCCACCTGGGGCTCC[C/G]CCAGTGTTGAACCCT	154214
rs745824569	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125067833	GTGGAAGTGATCACT[C/T]AAGGAGCAAATGCAA	154214
rs745826470	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125054542	ATCCTTTGTATCTCT[A/C]TGACACTCCTCAAGA	154214
rs745859844	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978811	GGAATAAGGTACGTG[A/G]ACACATGGACACCAG	154214
rs745876563	in-del	-/AATGAG			intron-variant	RNF217	GRCh38.p7	6:125031591	TCTTCACTGAATCAT[-/AATGAG]AGTCACCTTTGCTCT	154214
rs745896815	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993776	ATCTAAGGGTAAGTA[A/G]GAGTTAGCCAGATAA	154214
rs745908461	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040576	AGGAGGGACTCCTCC[A/G]TAACTCATTTTATGA	154214
rs745917783	snp	A/G	1.64836e-05	0.0028708	intron-variant, synonymous-codon, downstream-variant-500B	RNF217	GRCh38.p7	6:125009282	CAAGAAAGGGATGAA[A/G]GTAAAGTACATAGAT	154214
rs745933910	snp	A/G	1.67279e-05	0.002892	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081488	GGGATTGGCACTAGG[A/G]GCCATAGCGGTTGTA	154214
rs745934527	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038570	AGGATTCATAATACC[C/T]ATCTGCCAACCTTCA	154214
rs745990541	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980345	AGTTTATCTTCATTA[C/T]TTTTTAAAACAAATA	154214
rs745999091	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026532	CAAGCCTTTAGAGCA[C/T]TGAGAGCGTAAACGT	154214
rs746009754	snp	C/T	1.74824e-05	0.0029565	intron-variant	RNF217	GRCh38.p7	6:125045183	CCAGTGACGTTTTTT[C/T]CCTTCCATCTGCTCT	154214
rs746042832	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017745	ATTACATATTAACTG[A/G]CTGTATTTTTTTATT	154214
rs746055361	snp	C/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981470	TGGTTTGGTTGGGGG[C/G]GCGGTGACTTTCAGG	154214
rs746068539	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966296	CTTAACCTCTCTATG[C/T]CTTAATTTCCTCATC	154214
rs746076055	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013601	TTCTTTTAGTAAAGA[C/T]TTATAGAGTTCGTAT	154214
rs746087272	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027394	ATCCCAGAAATAAGT[A/G]AGAACATGCAATGTT	154214
rs746135918	in-del	-/ATG			intron-variant	RNF217	GRCh38.p7	6:125067653	GTGGTGAGCCATGAA[-/ATG]ATGATGAGTTTGGTT	154214
rs746154903	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967183	TTCCCAGTGACCTGT[A/G]TATGCGTGTGTGAAT	154214
rs746184175	snp	A/G	0.000164002	0.00905395	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962726	GAAGCGACTGGGGCT[A/G]CGCGGACACCAGCGC	154214
rs746211574	snp	C/T	1.67573e-05	0.00289454	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057955	AGATCCAGTGCCCTA[C/T]CTGCCAATTCGTCTG	154214
rs746214546	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053117	TGTCCCTGTAACATT[C/T]TACTCATTGTTGAAG	154214
rs746221166	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972152	AGATTCCCTGTTTCC[A/G]TTCATTGTACTCAGG	154214
rs746277994	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125050531	AATATTTTCTCATGT[A/G]GTAAAAGAATTTTCT	154214
rs746301595	snp	G/T	6.58711e-05	0.00573857	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962780	GGCCCCCGGGCTGGA[G/T]TAAGAGCCGAGCACC	154214
rs746309663	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125005116	ATAACCCTCGTGACC[-/T]TAAACACCTCTTAAA	154214
rs746364626	snp	A/G			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006544	TGCTTCATAAACTTC[A/G]TAATTAATTTCAATG	154214
rs746378039	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125039534	TTTTCAATATTAGAC[A/T]GATCAACAAGACAAA	154214
rs746399773	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125051438	ACCTTACATTTCTTA[C/T]CTACCACCCTCTGTG	154214
rs746456248	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022511	GCCCTTTTTCTTTCA[A/G]TTAGCACATTGAGTG	154214
rs746494550	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125066547	GCCAGCTCTCTCACT[G/T]CTTACATGTTTTTGA	154214
rs746495111	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125066640	TCCCCTACCTCAGTA[A/G]GTACTATCCCCTCCC	154214
rs746495340	snp	A/G	8.76079e-05	0.00661787	intron-variant	RNF217	GRCh38.p7	6:125048298	ATTTTTAAAAATTCA[A/G]TTTCCCTAATAAAAT	154214
rs746538972	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125068861	GTAAATATGAAAAGG[-/T]TGAAGGTAATCATTG	154214
rs746564090	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009657	CTTTTCTTTCTATTT[G/T]TTTTAACCTCTGTTG	154214
rs746587967	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054461	CAGAAGTCAATGTCT[A/G]TGTCCTTCTCCAGTG	154214
rs746622759	snp	A/C			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961284	AGGGAACTAAAACAC[A/C]AGTGTCTGGGTGAGT	154214
rs746641129	in-del	-/G	1.78833e-05	0.00299021	intron-variant	RNF217	GRCh38.p7	6:125045176	AAAATAACCAGTGAC[-/G]TTTTTTTCCTTCCAT	154214
rs746656377	snp	G/T	0.000242133	0.0110004	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962806	GCACCGGCGCAGCCT[G/T]CGGGACTGGCACTCA	154214
rs746665120	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125043168	TTCATCTTTAAGAGC[C/T]GTCCCAAGGCTGTGA	154214
rs746672837	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086493	ATGTTGCTTGACAGA[A/G]GAACTTAATTATGCC	154214
rs746761090	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125047227	GTAATTAAAACATGT[A/G]CAAAATTGAATTAGA	154214
rs746776287	snp	A/C	0.000337268	0.0129815	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963181	CGACTGTCCCTCCCA[A/C]CGGATTCCCTCTCCC	154214
rs746855765	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125000811	GTCCTAAGTGGATAA[C/G]TGTAGTAAAAAGATT	154214
rs746857351	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048474	TCTCTTTATAATAAT[A/G]TTTACAGGCTTAAGT	154214
rs746869843	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032772	TAAAAATTTGCATAA[A/G]AGGATAAGGGAGCAC	154214
rs746882912	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077525	CCCCTTCCCACACTG[A/G]TACACAAGTATGCAA	154214
rs746974090	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078540	GGCCAGCAAGCCCAC[A/G]AGACACAGAAAATGG	154214
rs747012318	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990807	TGGTGGCTTACGTCC[A/G]TAATCCCAGCACTTT	154214
rs747040358	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125004649	CTGTGAAGGCCTAAG[G/T]CTTTTTAAATGATCC	154214
rs747051913	in-del	-/CC			intron-variant	RNF217	GRCh38.p7	6:125068424	CTCCTCTGACCCTTA[-/CC]CACCAGATCAAGCTC	154214
rs747068755	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038320	TTAGATGACATGTTA[C/T]TTAGAATGTTAACTT	154214
rs747069996	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062021	TTGTAATTTCTCTCT[A/G]AATTATATCTTAAAT	154214
rs747075479	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125036242	TCATCCATGTCCCTG[C/G]AAAGGACGTGAACTC	154214
rs747091975	snp	C/T			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006238	AAGAAAAATAAGTTA[C/T]GAACTTTTGACTCGA	154214
rs747104875	in-del	-/ATTTTGTTACCAGGAC			intron-variant	RNF217	GRCh38.p7	6:125077018	AAATTTAAAACTTAA[-/ATTTTGTTACCAGGAC]ACTACTTATATGAGC	154214
rs747105987	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125039439	ATACAGGAGCACCCA[C/G]ATTCATAAAACGAGT	154214
rs747109737	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032878	CTGGTTTCATGAAAC[A/G]TTAATATCTCATTAA	154214
rs747181330	snp	A/G	2.12127e-05	0.00325667	intron-variant, missense	RNF217	GRCh38.p7	6:125082455	ATTATACAGTTGAGG[A/G]AATTAAGACTTACTG	154214
rs747191736	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025166	TAAAGTAAGGATTCA[A/G]ATGGACATTTAGTAA	154214
rs747197172	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979462	TAGAGAGATGAGAGC[A/G]GAATGGTGACAGCAA	154214
rs747248875	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125040304	TACCATCAGAGAATA[C/T]TATAACACCTCTACA	154214
rs747314394	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125073297	ATGTGGCTACAGTAA[C/G]CATTGATAAACATGA	154214
rs747316385	in-del	-/TGT			intron-variant	RNF217	GRCh38.p7	6:125013386	GTGTGTGTGTGTGTG[-/TGT]GCTGTTTTTGAGAGC	154214
rs747327168	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125029550	TGAAAAGGCTCCGTT[A/G]AAGTTTCTGTTAAAG	154214
rs747361151	snp	G/T	1.81519e-05	0.00301258	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962892	GGAGGAAGCTGGGGA[G/T]CGAAAAGAGGGAGGG	154214
rs747361613	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985088	TGATCCATACTAATA[A/G]GATAATTTAAATCAG	154214
rs747417302	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125030515	ATTCCAAATGGGAGC[C/T]ATTGGCCAAAAGGCC	154214
rs747432913	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125052605	TTCCCATATGGAGAA[A/T]TTCTTTCCATTGCCA	154214
rs747442361	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124989261	TTCTTTTAGTATAAC[G/T]ACAGTCTCACTGCAT	154214
rs747526261	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124986257	TGCTATTTCTATAAA[A/T]GCCTTACCTTCTTTT	154214
rs747545777	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086758	CAAGAAAACAAAGAT[A/T]ATTAAACACAAGTCA	154214
rs747571195	snp	A/G	1.68641e-05	0.00290375	intron-variant	RNF217	GRCh38.p7	6:125045202	TCCATCTGCTCTTCC[A/G]TCATGCAGGTACAAC	154214
rs747597384	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000617	GTATTCTAGGAAAAT[A/G]TGGTACATTTCAGAT	154214
rs747606155	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125032488	ATATATATTTCTTAT[C/T]TCCAGAATATTTTGT	154214
rs747618046	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971776	TGTTAAGTTTTAATG[G/T]CAACATACTCTCCTG	154214
rs747626589	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091670	CTATAGCTCCAATTA[C/G]GACAAAATTACTTTA	154214
rs747631715	snp	A/G	1.83293e-05	0.00302726	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962817	GCCTGCGGGACTGGC[A/G]CTCACCGGGCCTCTC	154214
rs747631936	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028327	GAGGACCCCAAGATA[A/G]GAGCACCTTTTCATA	154214
rs747673264	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077322	ATAGAGTTCCATTAT[A/G]TCTATATAAGTGATA	154214
rs747719121	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125002340	CCTCCTAATCCTCCT[C/T]GTCACAAGCTTCATG	154214
rs747721486	snp	A/G	3.64963e-05	0.00427163	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962905	GATCGAAAAGAGGGA[A/G]GGGATGAACAGCAGG	154214
rs747739879	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004401	CACTGTCTAGCCAAG[A/G]TAGTTTTCCTGTGGC	154214
rs747785663	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125022386	ATTAACAAAAATAAG[G/T]AACAATTAATGTTCT	154214
rs747811608	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124975590	CGTGCACCACCATGC[C/T]TGGCTAATTATTTTT	154214
rs747819349	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053342	CCTGCTACTTGAAGG[C/T]GCCCAATAAATATGT	154214
rs747819788	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125007850	GTACTGAACACTATA[C/T]ATACTATTTTTTAAT	154214
rs747873068	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083662	CCTATTGAAAGATGA[C/T]GGCTCCTTTGTGGAC	154214
rs747890775	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012371	ATATGTACAATGGAT[A/G]CTTTAAAGGTACTCC	154214
rs747915741	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125056581	AAGAGCTGTGATTGT[-/A]ATTGCCACTCAGCTA	154214
rs747917797	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125026374	ATCAGGAGTAACTGA[A/G]GTTAATCAATGGAAA	154214
rs747933222	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042215	AGAAGTATGAGTAAT[C/T]GAAGGATTGTATGAG	154214
rs747956220	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125058344	ATATAAATATTGACT[G/T]AAGACATTGAGGTCC	154214
rs748096540	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988081	TCCTATCAGGTCAGC[A/G]AAGGCATCAGATTCT	154214
rs748191203	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125058640	TGAATCCCACTTTTC[A/T]TCTTTCTTTTGATAA	154214
rs748196770	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125016906	CTGCACGTTCTGCAC[A/G]TGTATCACATAAAGC	154214
rs748207727	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125018364	TTTCTAGTATTTTCT[A/T]CAGAATTTGGCTTTA	154214
rs748230406	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049614	AATAGTACCTATGTC[A/G]TAAGAATGTAGTAAG	154214
rs748255133	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124970343	ATACAGGCGAACGCA[G/T]TTTGAACTGGTTGAA	154214
rs748257055	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125078962	TTCAGAGAGAAGATG[C/G]AGTATAGGAAAGCCC	154214
rs748258167	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002821	AATCTATTTGGTTCT[A/G]TTATAGCTAGATGAA	154214
rs748269051	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032357	AACTCCATACCCATA[A/G]TTCTTAATAATCTGT	154214
rs748318385	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125038218	AGCATCTTTTTCAGT[G/T]ATATAAATAGTTGTA	154214
rs748324715	snp	G/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967587	TATACACCTGTCCAA[G/T]GAGTATTAATAGATA	154214
rs748337393	in-del	-/CA			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091645	AGTTGAAATGACTCT[-/CA]CAGTTTTATCTATAG	154214
rs748344088	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004390	GATTGTACCAGCACT[A/G]TCTAGCCAAGATAGT	154214
rs748357265	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125074290	AGGTCGGTAGACAGA[-/T]AGATAGGTAGATAGA	154214
rs748391543	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009118	TGTTAGAAATGTATG[C/T]ATAAAGGGATTTGTT	154214
rs748476378	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995635	CCTATTGAAAAACAT[C/T]TGGAGGGCGGGTGCT	154214
rs748481513	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124996490	TTCTACCAATTCATG[A/G]TTTTCTTTTTCTATT	154214
rs748488246	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054195	ATCTGGTTGCAAGAA[A/G]TAGGGAAGACATCTT	154214
rs748506291	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125027618	GCTGCAACAAACAGA[A/C]GTGTAGAGATCTCTT	154214
rs748523475	snp	C/G	1.65518e-05	0.00287674	intron-variant	RNF217	GRCh38.p7	6:125076886	CATACTTATGGGTGT[C/G]TTCCCTGGGAATTAA	154214
rs748571143	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011255	AAATATTACATGTAA[C/T]TGGCTCTCACCTCCA	154214
rs748643173	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125073011	ACATAATAGGCTCTA[C/T]GCAAAAATTAGCGCT	154214
rs748669326	snp	A/T	0.000126542	0.00795331	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045475	AGAGCTGTGGGTTAG[A/T]TGTCACATGGCAGAA	154214
rs748673386	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125060736	AGGTATGAGCCACCA[C/T]GCCAAACCATATTTT	154214
rs748735746	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124984829	TCAGCTTTATTCCCT[C/T]TAAGCAAAGAATTCC	154214
rs748777735	snp	C/T	1.65072e-05	0.00287286	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076707	GACCTGCTCACAATG[C/T]AACACTAATTTTTGT	154214
rs748789029	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125074935	AAACAACACAATGAA[C/T]AGAAGCCTCCACTAG	154214
rs748797659	snp	C/T	2.58977e-05	0.00359836	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963008	TGGGTCAGCGGCGCC[C/T]GTCCCTCGCCAAGAG	154214
rs748801254	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049774	GGGAGTAAAAAAGAA[C/T]ATAGTTGAAAGAAAA	154214
rs748832942	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125016773	GGAACATCACACACC[-/G]GGGCCTGTGAGGGGG	154214
rs748850809	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999272	TCATGAGTTTCTAAC[C/T]GCAGGTGCACAAGGA	154214
rs748928205	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124999657	CCTTAGGGCTGTTCT[G/T]TGGATCAAATAAAAT	154214
rs749010592	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973834	ATAAAAAAAAAGAAC[A/G]ATTTTATTTTGATGA	154214
rs749010970	snp	C/T	5.31722e-05	0.00515589	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082917	CAGAGAAAACGATCA[C/T]GGACAGGTATGCACT	154214
rs749040062	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125024006	AGCAACCTATTGTAC[A/C]GTATGGTGACTATAG	154214
rs749059173	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125039186	GACATGGCCTCATTC[A/C]TTTTTATGGCTGCAT	154214
rs749062522	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125004096	TCATCCATCAAATAA[C/G]GTTGCCTTTCTTAGA	154214
rs749086852	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125068018	ATAAGATAAAAATTT[A/G]AAACATGTTCATTAT	154214
rs749102269	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125069104	ATTTGGACAGTATAC[A/T]ACACTTTAATGAATT	154214
rs749108264	snp	A/T	3.5868e-05	0.0042347	intron-variant	RNF217	GRCh38.p7	6:125058143	AAAGAAAAAACATGT[A/T]CATCTGGATGTGACT	154214
rs749133293	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125011392	TGGAAAATCAGAAAC[G/T]GAAGGCTCAGCGAGG	154214
rs749199301	snp	C/T	1.89188e-05	0.00307555	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962930	AGCAGGAGGCGCCCC[C/T]CGGCGAAGAGCTGGA	154214
rs749219755	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088307	TACCTTTTGGATGCA[A/C]ACCAATGATACAAAT	154214
rs749234241	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044475	CATGCTAAATGTTGC[A/G]TTTTGATGTATCCTC	154214
rs749264123	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090319	AAATGATTTTCTGTA[G/T]AAGGAACACAACAGT	154214
rs749298870	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092324	GGACACCTTGTGATA[-/T]TTTGGAGTCTAATTT	154214
rs749301404	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125071800	AGTACTAACAATTCA[A/C]ATGTCATTCATGATT	154214
rs749320528	in-del	-/CAGA			intron-variant	RNF217	GRCh38.p7	6:125056208	TGCTAAACTTGGAGC[-/CAGA]CAAACTTACGTTTAA	154214
rs749322162	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125027488	CAAGTGACAGGATGT[C/T]ATTCTTTTTTATGGC	154214
rs749347744	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125018484	TTGTTGAAGACTTTT[C/G]AAACACATTAGCATT	154214
rs749384627	snp	A/C			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983079	ATTTCTTCTTCAACG[A/C]TCCCCCCTCAACCAC	154214
rs749391883	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967212	ATATGGCTAAAGTAC[A/G]TAGTCCCAGGGATGT	154214
rs749400662	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960711	GTCTTAGCCTGTTGT[C/T]ACCTGGAAAATGCAG	154214
rs749411121	in-del	-/AGGG			intron-variant	RNF217	GRCh38.p7	6:125025580	GAAAAGAAGGAAGGG[-/AGGG]AGGGAGGGAGGGAGG	154214
rs749433623	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124992278	TTGTAATTAGAATAA[C/T]GTTTCCTAATAAAAC	154214
rs749501557	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125016865	GCAGCAAACGGCCAT[A/G]GCACGCGTATACCTA	154214
rs749640826	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058245	TTTTATTTTGGAAAA[A/G]TAATTATATAATTAA	154214
rs749644448	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125007649	TTTGTGGTGACTAAT[G/T]CTTCTAACATGTTTT	154214
rs749670061	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092292	CACAAATTTTAGGGA[C/T]AAGTCTTTCAAAAGA	154214
rs749676161	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040810	CAATAAACATTATGT[A/G]ATCATAATCACATAA	154214
rs749681733	in-del	-/T	0.00015259	0.00873337	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971577	TCTCCTGCCTCAGCC[-/T]TCCGAGTAGTTGGGA	154214
rs749743289	snp	C/T	1.67139e-05	0.00289079	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081481	TGGTTTTGGGATTGG[C/T]ACTAGGGGCCATAGC	154214
rs749790130	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995405	AATTTAGTTTCATTA[C/T]AAATGTATGCATCCC	154214
rs749803571	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125041719	ATGTGTAGTTCATTC[A/T]TAACACAGGTTACAA	154214
rs749804095	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026734	AGTCCTTAAACTCTG[C/T]AAGAATTGCACTGCT	154214
rs749823378	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084524	CTGATTTGAAATAGA[C/T]GATATGATAAAACAT	154214
rs749833285	snp	A/G	1.65921e-05	0.00288024	intron-variant	RNF217	GRCh38.p7	6:125076902	TTCCCTGGGAATTAA[A/G]TAGTGAAAATAGAAC	154214
rs749863755	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125069260	TAGCAAGAGACACCA[A/G]ATAATTTTGAAATCA	154214
rs749868149	snp	C/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981593	GCCTTTTTACATAAA[C/G]AGCAAGGCAGAGAAA	154214
rs749893135	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125024882	TCTGGACTGGTGTTT[C/T]AACATGTGGGAGCTT	154214
rs749898913	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040026	CAACACCCTAACATC[A/G]CAACTGTAGAGAAGC	154214
rs749899791	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068958	AGGTGAAGATGAAGC[C/T]GAAGGAGGGGAAAAC	154214
rs749980596	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025825	TGTACTCTCTTATGA[A/G]TGGGGAACAGAAAGT	154214
rs749982220	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988695	TTGTACTGAATTTGT[A/G]TTTTCTCAATTTGTT	154214
rs749991888	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057214	ATGGTCTCTCTCTGT[C/T]GCCCATGCTGGAGTG	154214
rs749999961	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125012657	CCTATGTTTTCCTTT[C/G]GTGCTCCTTAGCATA	154214
rs750047219	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125044878	CAGTTGGTGCATCAT[C/G]TGAATGCTGTCTAAC	154214
rs750057889	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075331	AATTGTATTAGTCCA[C/T]TATCATGCTGCTATG	154214
rs750124010	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990547	TTTCCAGTTGCTTAG[A/G]CCAGAACTTTGGAAT	154214
rs750145380	in-del	-/TGTAGTAATATTT			intron-variant	RNF217	GRCh38.p7	6:124998813	AAAAAACAAAAATTG[-/TGTAGTAATATTT]TGTCAACATAAGATT	154214
rs750149463	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125018130	ATAGAGACATGGTAT[A/G]AGGGCTCCTTACTTT	154214
rs750173755	snp	C/T			intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971513	CAGGCTGGAGTGCAG[C/T]GGCATGATCTCGGCT	154214
rs750211974	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125051722	TTCCCATTTCCTTAT[G/T]TACACTTAACACAGT	154214
rs750215693	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089996	GATAAAGTATCATAA[C/T]TTCATTATCAGCTGA	154214
rs750251821	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124984542	CTGAGACCCTTTCTC[-/A]AAAAAAAAAAAAAAA	154214
rs750273232	snp	G/T	4.78503e-05	0.0048911	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962748	CACCAGCGCCCCAGA[G/T]CCCGCGAGGAGCCTG	154214
rs750275416	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125064844	GTATGTACGTGTGTA[-/TA]TATATATATAGTTAG	154214
rs750296148	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124992375	AATGAAAACTTGATA[A/T]ATAATAGTCAAGCAG	154214
rs750311541	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053929	AGGACAATGTATTTA[A/G]TAAACATCATCTGAT	154214
rs750367155	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125050918	GAGACAGTTAAAGTC[A/G]TCTAGCCCTGTTGAT	154214
rs750393778	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081599	ATGAATCAGTTATTA[A/G]GTGGACATAATTTAT	154214
rs750400819	snp	A/C	6.7769e-05	0.00582065	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081522	GGTAAGAAACACTTC[A/C]TGCATCTGAGATTAG	154214
rs750429258	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053151	ACATTCTCTCTGAAC[A/G]CTTATGTTCCAGCTT	154214
rs750430705	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993416	TATTATCATTAGCCC[A/G]TCTGTTAACCAAACT	154214
rs750459646	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065477	CATTGCAGGACATAC[A/G]TAAATGCCAGCCCCA	154214
rs750462662	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007395	GGATTATAGGCATGC[A/G]CCACCAAGCCCGGCT	154214
rs750464920	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022143	TACCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	154214
rs750468480	snp	C/T	2.14549e-05	0.0032752	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962973	CGTGGGGGCCGCCGA[C/T]GGACTGGTCCTGGAC	154214
rs750507353	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090234	TACAGATTTTTAATA[C/T]GAAAATTGACAATTT	154214
rs750517659	in-del	-/GTGA	1.67944e-05	0.00289775	intron-variant	RNF217	GRCh38.p7	6:125082402	TTAAGTTCTTGCAAT[-/GTGA]GTTAGGACATTATGT	154214
rs750523695	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067311	CCTCCAGACTATAGG[A/G]GCCATTGAAAAATAA	154214
rs750540658	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040882	GCAGAAAAGGCCTTC[A/G]ATAAAATTCAACATT	154214
rs750549667	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041584	AGGCAAATCAGACAC[C/T]TTCTGACTGGAGCCA	154214
rs750554622	in-del	-/AGAA			intron-variant	RNF217	GRCh38.p7	6:125012580	ATTTGACATATTCTT[-/AGAA]AGCATTAGTTTTGTG	154214
rs750554915	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125008643	GCTTTGTGCATTCAG[A/G]TCAGGTCAAGATTTC	154214
rs750587023	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084275	CTGCTTTTGGGAAAG[C/G]AAACAAAAAAGTGAA	154214
rs750628959	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086237	ATTTTTAAAGAAAAT[C/T]GTCTTTTGAAGGGTA	154214
rs750668845	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124997149	GAGAAGAGAATTTCT[G/T]TTTTGACCAGGCATA	154214
rs750723569	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982819	AAAGTTGATGACTTT[A/G]TGGTATGTGAAAGTA	154214
rs750748106	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046126	ACAGATAAACCTGGT[A/G]AGCATTTCAGAGCAA	154214
rs750770051	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125077857	CCTTAGCCCTTGGTC[A/C]CTTCATGACTGTTGT	154214
rs750791708	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075822	ATGAGGATTCTGAGT[C/T]GAGTTTCCAATTTTA	154214
rs750792248	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987901	TGTTGTGATTTTAGA[C/T]TGGATTAATTAACAT	154214
rs750802784	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125079827	ATATTTAAATAAAAT[A/G]CGATATATGGATATG	154214
rs750811303	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000258	CTAGAAACTAAAAAT[A/G]TATTCTGTTGAATGG	154214
rs750815892	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994279	ACTATTTTGTTGCGT[A/G]TCTATTCCCACTCAC	154214
rs750880797	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124996138	TTGATACTCGCTCCA[C/T]AGCTGATGAAAGTTC	154214
rs750882032	snp	A/C/T	4.96877e-05	0.00498415	intron-variant	RNF217	GRCh38.p7	6:125076890	CTTATGGGTGTCTTC[A/C/T]CTGGGAATTAAGTAG	154214
rs750882313	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988603	CTAGCTTTTTAAATT[C/T]GTCAAACTAAGCCTT	154214
rs750897491	snp	A/G	5.43375e-05	0.00521208	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962870	AGTTGGAGCTGGAGG[A/G]GGAAGAGGAGGAAGC	154214
rs750903912	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125065440	GAAAAGCTCAATTCT[G/T]TATTGTGCAGGATAT	154214
rs750945293	in-del	-/C	0.000180457	0.00949714	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963313	GGGGATCCCTATGTG[-/C]CCCTCATGGTGCTGA	154214
rs750968427	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124975067	GCTATTTGCCTCAAT[A/T]ATATTCTCTACTGTA	154214
rs750987582	snp	A/G	1.66065e-05	0.00288149	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045229	CAACTTGGCCAAGTA[A/G]AAATCAAATGCCCCA	154214
rs751025752	snp	A/C	1.67287e-05	0.00289207	intron-variant, missense	RNF217	GRCh38.p7	6:125082491	TCATAAGTGGTAGAA[A/C]CAGGAATCAAACCCA	154214
rs751042394	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125079898	CTAGGAATAAGAGAT[A/C]GTATGCCTAGTCCCT	154214
rs751045014	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125031909	ACATACACAAGACTG[C/G]GAAGAAAAAGAGGTT	154214
rs751050418	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061487	ACCCTTTGCCCATTT[A/G]TGTGGGACAGATTGG	154214
rs751072111	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125038777	TTTCTATCACCTATC[C/G]TATTGTTAGGAGCTT	154214
rs751130419	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125067633	GTTATTTATTTTTTG[C/T]TGCAGTGGTGAGCCA	154214
rs751132420	snp	A/C			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081528	AAACACTTCATGCAT[A/C]TGAGATTAGAATTAT	154214
rs751159754	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125024658	CCGGGAGGCAGAGGT[C/T]GCAGTGAGCCAAGAT	154214
rs751178208	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125055027	GGAAGATGCAGTGTT[A/G]ATGTCTGTATGTGTT	154214
rs751200818	snp	A/G	1.67178e-05	0.00289113	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081468	GCACCTCTAATTATG[A/G]TTTTGGGATTGGCAC	154214
rs751207476	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978680	CAGTGGGCAGAAGGG[A/G]GGGTTACAGATCATT	154214
rs751209054	snp	C/T			intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964134	TTTTTTCTTGGAAAG[C/T]TTGAGAGTGCACCAG	154214
rs751224133	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068508	TAGCTTATGAATATA[C/T]ATTTGTTAGTACAAT	154214
rs751247106	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012503	TCTTCTGTTTAAAAT[A/G]TATTTGCATGATTAT	154214
rs751251800	in-del	-/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960673	TGGGAATATACTTTT[-/T]GGCATCCATTATTGT	154214
rs751270800	snp	A/T	3.30923e-05	0.00406756	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058064	CTGGGCCAGCGAAAT[A/T]GAGCATGGGCAGAGG	154214
rs751278428	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125072617	ACAGATATAAAATTA[A/C]AGTGAAAATTATATG	154214
rs751278780	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:124984724	AAATTTTAAGTGTAC[-/TA]GTAGAACTGATTTTC	154214
rs751334453	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125029319	TATATATTCTTTTAT[G/T]TTTTCATATTCAAAT	154214
rs751345946	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125016857	TGATGGGTGCAGCAA[A/T]CGGCCATGGCACGCG	154214
rs751360897	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125059894	AGAACCATGGAATCA[A/G]TGGACATTATTACAT	154214
rs751378194	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049008	TCCATAGTATTTCTG[C/T]CTTCTTCTCCCTAAA	154214
rs751461158	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970002	AAGATAGAAGCATAC[A/G]TGTGAGTTTCCAGGA	154214
rs751523037	snp	A/G	1.65004e-05	0.00287227	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009334	GCTGCAGGAGCCCTT[A/G]TAATCTCTTCAAAAC	154214
rs751546727	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049253	CATCACCCACACCCA[A/G]AGCTTTTCACCATAG	154214
rs751554325	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125064259	ATTTTTAACTCTCCA[G/T]ATTGCTTAAAATCAC	154214
rs751566025	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124971313	AGACACTTAATTACA[C/T]GTTTTGAGGAAGCGA	154214
rs751573397	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085253	TCCAATATTCCTGTT[A/C]CAAAGTGGTGTCTGT	154214
rs751613339	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027740	TCCAAACTGTTGTCC[A/G]TAGTGGTTGTACTAA	154214
rs751703221	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125000823	TAACTGTAGTAAAAA[G/T]ATTTCTTTAAAAATA	154214
rs751719778	snp	A/G	1.89626e-05	0.00307911	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045449	GCAAATACAAAGTAA[A/G]CATTTTCACCAGAGC	154214
rs751720986	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125021031	AAGCAGTTTGGCAAT[A/G]TGTGTTAAAAGTCTC	154214
rs751759407	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978299	GGGACTTCTGGGCTT[A/G]CTCCACCTGCTTAGC	154214
rs751761843	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089431	TTGGGGTGGATTTAT[A/G]TAGTGTAGCATTTGT	154214
rs751764665	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124974620	ATCAAAATTACAGCT[C/T]CAGCTGTAGTTAAAA	154214
rs751776805	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053002	ATCTCTGTTCAGGCT[A/G]CATTAGAACACTTGC	154214
rs751787301	in-del	-/GACACCAGCGCCCCAGA	0.000113682	0.00753843	frameshift-variant, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962731	GACTGGGGCTGCGCG[-/GACACCAGCGCCCCAGA]GCCCGCGAGGAGCCT	154214
rs751860169	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011965	CACCAGGAGGGGCTG[A/G]CCAGATGCATCTTTA	154214
rs751889346	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025563	AAGGAAGGAAGGAAG[A/G]AAGAAAAGAAGGAAG	154214
rs751932509	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087658	TCTTTAAATTTGGGA[A/G]GAATCAGAAGCTAAA	154214
rs751934851	snp	A/G	1.65285e-05	0.00287471	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076670	AGATCCACATCCAGC[A/G]AACTGAAGGATGTGA	154214
rs751942507	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124965347	GGGAGGCTGAGGCAG[G/T]TGGATCACCTGAGAT	154214
rs751944245	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012925	AGAACTTCTAGTAAA[A/G]TATCTTTGAACAACC	154214
rs752020619	snp	A/G	2.18357e-05	0.00330415	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962979	GGCCGCCGACGGACT[A/G]GTCCTGGACGTGCTG	154214
rs752024741	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125043311	CTGCTTGAAACCCCT[C/T]CTCACTTTTGTTTGG	154214
rs752034204	in-del	-/AGT			intron-variant	RNF217	GRCh38.p7	6:125019831	TGTCCCCTTTTTTGC[-/AGT]GGGGGGGGAGTGAAA	154214
rs752062615	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125077684	CTCTGGAATGTAACC[A/C]TGTGAGATTTCTTCC	154214
rs752072282	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987861	AATGATTTTACTGCA[A/G]TATTAACTTGTACAT	154214
rs752110814	snp	C/G/T	0.000218227	0.0104438	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963066	GGAGAGCGACCTGCC[C/G/T]GAGGCCCCCGCCTCG	154214
rs752128253	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124993964	TTATTCTGCAGGTAG[G/T]GGGCAGTGATTGAAA	154214
rs752177491	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125079709	AAATTTGATACTAAT[A/G]TGAAGGCCATTTTAA	154214
rs752185571	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125016720	GTTCTCACTCATAAG[C/T]GGGAGCTGAACAATG	154214
rs752188021	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124969651	CTTATGTATTAAATA[C/T]TTATTACATACAAGG	154214
rs752189012	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049136	GTAATTTATCAGTGC[A/G]ACAGCAACCGCTTAT	154214
rs752206994	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061243	ATTTAGCACATATTG[A/G]CAATTTGCTTTCTAA	154214
rs752209665	snp	C/T	1.65143e-05	0.00287348	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076689	TGAAGGATGTGACCA[C/T]ATGACCTGCTCACAA	154214
rs752211680	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057879	CCCAAGCATCACCTT[C/T]TTATCCTTTTAGACA	154214
rs752274469	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124999193	TGAGACTGGCTGATC[-/T]TTGGTATATTTCATT	154214
rs752331064	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966399	TATTTTGTTGCCCTA[C/T]TGAACCACATCAAAA	154214
rs752335531	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031745	TTCCCACATTTTCCT[A/G]TCTTCTTCTGAGCCC	154214
rs752356642	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124977031	TAAAACAAACTGTTC[A/G]TACATGCTTTTCTCT	154214
rs752370340	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990704	TGCCACCATCATTCT[C/T]ACCAGGAATCTAGCA	154214
rs752405066	snp	A/G	2.40856e-05	0.00347019	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962999	TGGACGTGCTGGGTC[A/G]GCGGCGCCCGTCCCT	154214
rs752423590	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007018	GTTTTTTATTTGTTC[G/T]GTTACAGTAATTATT	154214
rs752431361	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041461	TTTTTACCATGGCCA[A/G]CAAGGCCCATGTGAT	154214
rs752433683	snp	C/T	1.64746e-05	0.00287002	intron-variant, stop-gained	RNF217	GRCh38.p7	6:125082520	CAACATTTGGCTCCA[C/T]AGCCTGTGTTGTTAA	154214
rs752450501	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995812	CTGTAATCCCAGCTA[C/T]TCGGGAAGCTGAGCT	154214
rs752490439	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981394	CAAGGTGGTCGGGGT[A/G]CAGCTTGCTTTTATA	154214
rs752511178	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125070645	TGTTGGTATCTCTTC[C/T]TTTGAGAAATGTCTA	154214
rs752511595	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084192	TGCTCAAACATAATA[A/T]TTTTGGGGACACCTT	154214
rs752527460	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125042497	GTTCAGTGTAGTAGG[A/T]TAGGGATTTTGGAGC	154214
rs752528685	snp	A/G	1.64904e-05	0.00287139	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076808	GATGCAAATATCGCT[A/G]CCTCCCAGAGAGACC	154214
rs752579206	snp	A/G	1.67469e-05	0.00289364	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045403	ACCTTCAAGAAAAAA[A/G]GACATATTCCCACCC	154214
rs752579691	snp	G/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981589	ATCTGCCTTTTTACA[G/T]AAACAGCAAGGCAGA	154214
rs752580304	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982511	ATGGGAAAATTCTGT[A/G]GTCTAATCCCCACCC	154214
rs752592128	snp	A/C	3.30568e-05	0.00406538	synonymous-codon, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045276	ATTCTTGGAAGAAAC[A/C]ACTGTTGTCTATAAC	154214
rs752592833	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046814	GCTTCTTCATGAGTC[A/G]TTGTTCTTTGAAACT	154214
rs752621941	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124984323	AAGGCAAGGTGGGTG[C/G]ATCATTTGAGCCCAA	154214
rs752660892	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125030390	AGTCCACAGTCCAAA[A/C]TCCCATCTGAGACAA	154214
rs752672164	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968289	AAAATTTGAAAAGTG[A/G]GAATTAAGGCATATT	154214
rs752737638	snp	A/G	3.46765e-05	0.00416378	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048229	GGCACCCTGTACTGA[A/G]ACTAAGATCTTTGTT	154214
rs752768800	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044759	TTAAAATAGTAAAAT[A/G]TGCCCAGAGTTTAGT	154214
rs752825993	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124985986	GTGTTGAAACTCAGC[C/G]ATCAATGCAATAGTG	154214
rs752892655	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025655	GAAGGTGTTCTAAGG[A/G]AGGGAGGGAGTGAGG	154214
rs752896080	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125000557	TCCTTAAATATTTAT[A/T]ATTTTATAATTTACT	154214
rs752907010	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124998779	CTCCAACCTGGGCAA[A/C]AGAGCGAGACTCTGT	154214
rs752912953	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987696	GTCCAGGCTGGCTTT[A/G]AACTGCTAGGCTCAA	154214
rs752924004	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125063770	ATTACCACCATTTCA[A/C]GATGCAGAACCAGTT	154214
rs752926568	snp	A/G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084976	TTTGGCAATATGTGA[A/G/T]TATGATGAACTCTAA	154214
rs752926966	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125020712	CTCACATAGAATATT[A/T]TATAATCTCCATGAA	154214
rs752981089	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125005764	AAACTGTATGCAATA[C/G]AAAGCTTTCAAATAT	154214
rs753004074	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124972722	CTAACTCTCTTTGCC[C/T]CATTCACACCCATTC	154214
rs753065523	snp	A/G	1.87905e-05	0.00306511	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963084	GGCCCCCGCCTCGGA[A/G]CAGCTCTCGCCGCCC	154214
rs753066346	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125067553	AACCACCAAATATTT[A/C]GTATGGGTATCTAAA	154214
rs753093311	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125024637	GCACGAGAGAATCTC[C/T]TGAGCCCGGGAGGCA	154214
rs753138406	in-del	-/TGTT			intron-variant	RNF217	GRCh38.p7	6:125052320	GTGTGTGTGTGTGTG[-/TGTT]GTTTTATTTGTTTTG	154214
rs753161551	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124974073	GCCTCCCCCGGAGCC[A/C]GCATCCCAAGGGATG	154214
rs753165420	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054897	AGCCACAAGGACAGG[A/G]CATGATGATTTCTGT	154214
rs753167699	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125019833	TCCCCTTTTTTGCAG[-/T]GGGGGGGGAGTGAAA	154214
rs753192670	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965155	GGTCATTGCAGTGTA[C/T]AGTACAACCACTAAA	154214
rs753203438	snp	C/T			intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124963753	AAGAGACTGCCTCAT[C/T]GGCCTGGTATCCCAG	154214
rs753213558	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997472	AACTCGAGTTAATAT[A/G]TTCCCATCTCAAATA	154214
rs753249696	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125071262	ACCATATTTCAAATT[C/T]TGAATTTCGATCTTT	154214
rs753251487	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125056675	TAACCTTTAAAATGT[A/C]GTCAGTGAATTCACA	154214
rs753343912	snp	C/T	1.92465e-05	0.00310208	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963092	CCTCGGAGCAGCTCT[C/T]GCCGCCCGCGTCGCC	154214
rs753376977	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075414	ATGGTTCCGCATGCC[C/T]GGGGAGGCCTCAGGA	154214
rs753398941	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125000442	TGTAAGGGGGCATTA[C/T]AGATATCAGACAATA	154214
rs753399509	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124966921	TTTGTTTTTCAAAAC[A/G]TAGTTCTTCTCCAGT	154214
rs753414168	in-del	-/AAGTTGGTTATTAA			intron-variant	RNF217	GRCh38.p7	6:124966119	AGTAACAGGTTTGCT[-/AAGTTGGTTATTAA]ACTTAGAATTTAAGA	154214
rs753420504	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125014636	CAGAAGCAGTTCAAA[A/G]TCACACACACTAAAA	154214
rs753454029	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125077034	TTTTGTTACCAGGAC[A/C]CTACTTATATGAGCA	154214
rs753488523	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125047569	GGGCAAATGGACCAA[C/T]ATCTTAAATTTATTA	154214
rs753503487	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988833	TCACTTCAAACTCAG[C/T]ATTGACTCCTCAAAT	154214
rs753529959	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125051134	GGTTTTTAACTTGTG[C/T]TTGAACTTCTAACAG	154214
rs753534274	snp	C/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962069	GCTGGCCAGCGCTCC[C/G]GCTGCACCTCCTGGT	154214
rs753582450	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002133	ACTAATAATCTCCAG[A/G]ATGGCTTACTTTGAT	154214
rs753586704	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011565	TTTAAATATAATTAC[C/T]TGGAAAAAAATCACT	154214
rs753627734	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088219	AACAAATAATTTTAT[A/G]GAAGCATTAAAGTAT	154214
rs753637899	in-del	-/TAGG			intron-variant	RNF217	GRCh38.p7	6:125074294	TCGGTAGACAGAAGA[-/TAGG]TAGATAGATAGATAG	154214
rs753640165	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124993490	TGAGAGAATAAGATC[A/T]TTCCTCAGTTGCGCA	154214
rs753640394	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007090	GTTATCCAGTTCACA[A/G]ATTTTGTCTTCAGCT	154214
rs753719074	snp	G/T	1.81233e-05	0.00301021	intron-variant	RNF217	GRCh38.p7	6:125081417	GACTCCTTAAATAAT[G/T]TTGCCTTTTGTTTTC	154214
rs753735266	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125067893	TTGGTGAAGGAACAG[C/G]AACCTCAGAGAGGAG	154214
rs753755300	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979134	TTCAGGCTTCAGGCT[A/G]TCTTGGCTTGAAGGT	154214
rs753803130	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041426	ACCAGTGATTTGTAT[C/T]GTCTTTATATAATAC	154214
rs753807024	snp	G/T	1.64999e-05	0.00287222	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076844	TAAGGAGATTAGTGC[G/T]AGGGTCAGTCTGTGG	154214
rs753829693	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125070319	TGCTATAAACATGTG[C/T]GTGCACATGTATTTT	154214
rs753872228	snp	A/G	0.000100336	0.00708223	synonymous-codon, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962772	GAGCCTGGGGCCCCC[A/G]GGCTGGAGTAAGAGC	154214
rs753898837	snp	C/T			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963591	TAAGTGTATTATGAC[C/T]TCACTGGTTTACTTA	154214
rs753908134	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125028526	TGGAACTACACTGAG[C/T]TTCTCACTGTATATA	154214
rs753911730	snp	G/T	1.65241e-05	0.00287433	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058039	AAAAAGGAGACAAAT[G/T]GTTGCGTCACTGGGC	154214
rs753923037	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054762	AGGATGCATACAAAT[C/T]ACCTTCGGACCTTGT	154214
rs753964563	snp	A/G	1.81043e-05	0.00300862	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962862	GCCACTGCAGTTGGA[A/G]CTGGAGGAGGAAGAG	154214
rs753976696	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124997321	TGTATTACAATCCTG[G/T]TGCTTAAGTCATGAC	154214
rs754008428	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125046466	CATGACACACCAGTG[-/C]CCCCAGGCCCACCCC	154214
rs754070931	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998095	TCTTCCAGACCATTC[A/G]CCACTTCATCCTTTC	154214
rs754073945	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030207	TCCCTCCCACAACAC[A/G]TAGGAATTCTGAGAG	154214
rs754133359	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124970170	GTTGTAAGAAGATAC[G/T]GAGCAACAGACTAAC	154214
rs754133740	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985107	AATTTAAATCAGCAA[A/G]ACCAGATAGTGTCTC	154214
rs754141022	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125036142	CCGTGTGTTCTAATC[G/T]TTCGACTCCCACTTA	154214
rs754178282	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124992888	CCACTCATCTTTTAC[C/G]TAAAACGATTTATGT	154214
rs754179975	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125053628	CTGTTTTTATTTTGT[-/G]GGTTGTTTCCTTACT	154214
rs754218765	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975386	ACAGGTGACTCTGAT[A/G]TGGCCAGATTGTAGC	154214
rs754230682	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037597	AAAACCGTATGTGTC[A/G]GTAGAGCAGGCACCT	154214
rs754231286	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990607	CATTCTTATTTTTCA[C/T]GTGTGATTGTTAGAT	154214
rs754256145	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022325	CCATTATATACAGTA[C/T]GAATTCAGTGAAATT	154214
rs754299678	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967123	TATTATTCATATTAT[A/G]TTGCTCGTGTACATA	154214
rs754300678	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125035618	TTTGTTTGCATTTCT[G/T]CTCTCTTAAAAATAT	154214
rs754306738	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976966	CCCTGAAAGGATAGT[A/G]ATTTTTTCCTGATAC	154214
rs754319081	in-del	-/GTGA	3.31895e-05	0.00407353	intron-variant, splice-donor-variant	RNF217	GRCh38.p7	6:125082564	CTGCCTGAAACAAGT[-/GTGA]GTATCATAGTGTGCA	154214
rs754366612	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125010594	GTTTAAACAAGCTTA[A/T]GTTTATTTTATGCAA	154214
rs754381165	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090363	TAACAAAGAACCAGT[A/T]GTTTTGATTCTATTT	154214
rs754394457	snp	A/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960798	AAGGCACACATAAGT[A/G]GGTTTCTTGTCTCTG	154214
rs754398064	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125054149	TTAGACATCTACATC[A/C]CTAATGGAAGTTCCA	154214
rs754403069	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125013329	GCCAAAAAGAAAGGT[-/A]AGGTGCTTGCATGTT	154214
rs754403541	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124999310	ACTTCAAGCTGGCAG[A/G]GATTCATTTCTTCCT	154214
rs754479701	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052450	AGGCAAGGATCACTT[A/G]GCCACATTTGGACTG	154214
rs754483791	in-del	-/TGTGTGTGTG			intron-variant	RNF217	GRCh38.p7	6:125071485	GCATCTGCCTACATA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	154214
rs754496303	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125014753	ACAATCTTCCCATGA[A/G]CTCATTTTTGTGATG	154214
rs754501300	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125059454	CTCAGTTTCAAACAA[A/C]ACAAAGACCAGTAGG	154214
rs754535530	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968135	ATATTTTTGGAAACC[A/G]TTGTGTTCAGTGTTG	154214
rs754554490	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032428	AGTTCTGCATCTAAT[A/G]TCTACCATAGTTAGG	154214
rs754557637	in-del	-/AAAG			intron-variant	RNF217	GRCh38.p7	6:125028301	AGGTGAACAACACAC[-/AAAG]ATAATTTGAGGACCC	154214
rs754560646	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125048064	TTTTAGTGTAAAGTT[C/T]ATATAACATTTTTCA	154214
rs754589515	snp	A/G	3.48778e-05	0.00417585	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081555	TTATCTGAGGGCCAT[A/G]GAGAGAATACGAGTG	154214
rs754631930	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088235	GAAGCATTAAAGTAT[C/T]ATCAGAACAAAATCA	154214
rs754634716	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125078119	TTAATGATTTTCCAG[C/T]GCGTGCCGCTTCTTA	154214
rs754646178	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125036145	TGTGTTCTAATCGTT[C/T]GACTCCCACTTATGA	154214
rs754649830	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988857	CTCAAATAAACAATA[A/G]CAGTTAAGCCGTATC	154214
rs754688615	in-del	-/AGT			cds-indel, nc-transcript-variant	RNF217	GRCh38.p7	6:125089975	TTCTTTATAATGAAA[-/AGT]CTAGATAAAGTATCA	154214
rs754714016	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993509	CTCAGTTGCGCAAAT[A/G]TTCACTGAGGGCTTT	154214
rs754716429	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003933	GGGAACTCAGAACTA[A/G]TTGATCAACATCTGT	154214
rs754718844	snp	A/G	1.81681e-05	0.00301392	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962894	AGGAAGCTGGGGATC[A/G]AAAAGAGGGAGGGGA	154214
rs754719183	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029896	TCCCATAGGGCTTAG[C/T]TTACTTGGGACATAG	154214
rs754719829	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065904	ACTCAACATCTTCAA[C/T]CGGATCTAATAGACT	154214
rs754720797	snp	A/T	1.65176e-05	0.00287376	stop-gained, nc-transcript-variant	RNF217	GRCh38.p7	6:125076683	GCGAACTGAAGGATG[A/T]GACCATATGACCTGC	154214
rs754738624	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124979146	GCTGTCTTGGCTTGA[A/C]GGTCGGGTTTCACCA	154214
rs754778559	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040249	GACACAATAAAAATG[A/G]TAATGGGGATATCAC	154214
rs754805262	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125069131	AATTCTTGTCATTAT[A/C]AATTAATCATAAGAC	154214
rs754882180	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027172	AATCCAATTACATTA[A/G]GTTATTTTAAAATAC	154214
rs754893052	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125057388	GGTTTCACCATGTTG[G/T]CCAGGCTGGGCTTTA	154214
rs754941339	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965958	TGGTATATAACAGAT[A/G]GGCAACTAAAACCTA	154214
rs754956424	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046520	TGAGCCTCACCAGGT[A/G]ACTAATCCACAGTAG	154214
rs754975390	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013409	TTTTGAGAGCATGGT[C/T]GTGGAACGGTTCATT	154214
rs755009607	snp	C/G	2.00495e-05	0.00316613	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045461	TAAGCATTTTCACCA[C/G]AGCTGTGGGTTAGAT	154214
rs755029109	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125021022	GCTTTTAGAAAGCAG[A/T]TTGGCAATATGTGTT	154214
rs755054228	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125072810	GATCTTCTGGTGTTA[A/C]CTTTTAAGTTCATCA	154214
rs755077211	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125030229	TTCTGAGAGATACAA[G/T]TCAGGTTGAGATTTC	154214
rs755114474	in-del	-/TGTGTGTG			intron-variant	RNF217	GRCh38.p7	6:125071487	ATCTGCCTACATATG[-/TGTGTGTG]TGTGTGTGTGTGTGT	154214
rs755115349	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125016892	CCTATCCAACAATCC[C/T]GCACGTTCTGCACAT	154214
rs755142145	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125074197	CATGTATGAAGTGCC[C/T]GCCTGTAATATGCTG	154214
rs755143013	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994716	TTTTCTTTTGTGCTA[A/G]TAAGTGCTACTTTAG	154214
rs755154911	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124970272	GGAAGTAAAAAGATC[A/C]GTTAGAAGACTATGG	154214
rs755203262	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125018135	GACATGGTATGAGGG[C/T]TCCTTACTTTCAAAT	154214
rs755251218	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985841	GCAGAATGATAAAAT[A/G]TTAACATTTATTAAT	154214
rs755285104	in-del	-/GTTC	1.6483e-05	0.00287076	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009264	CACACCCATAAACCA[-/GTTC]AAGAAAGGGATGAAG	154214
rs755302722	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997055	GGACGTGCTGGTAGA[A/G]TCTATTTTTTCATCA	154214
rs755355296	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009078	GAACAAGGAAGTAGA[C/T]AGAATGTGCTTTCCT	154214
rs755384395	snp	G/T	4.46678e-05	0.00472566	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962986	GACGGACTGGTCCTG[G/T]ACGTGCTGGGTCAGC	154214
rs755388156	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053266	TATCTGTCAGACCCC[A/G]GTAAGTTCCTTAAGG	154214
rs755449046	in-del	-/AGGG			intron-variant	RNF217	GRCh38.p7	6:125025577	GGAAGAAAAGAAGGA[-/AGGG]AGGGAGGGAGGGAGG	154214
rs755470633	snp	C/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960963	GTCAGACCGATAGAT[C/G]ACATGGCATTTAGAC	154214
rs755535913	snp	A/C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086446	ATTGGTGATACTTTT[A/C/T]GCATTTTTAGTAACA	154214
rs755544826	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995991	TTTTTCTATTTCTCT[C/T]ACAGACTATGTACAT	154214
rs755545073	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042948	TAACAAGTGCCTCTC[A/G]AGGTGGCCCAAGTAA	154214
rs755549920	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012159	AAGGAATAAAAAACT[A/G]TGAAGGAATAGGAAG	154214
rs755649065	snp	A/T	9.9072e-05	0.00703749	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076693	GGATGTGACCATATG[A/T]CCTGCTCACAATGTA	154214
rs755651984	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125025971	GAGGGAGGTGAAATG[G/T]TTCATGGGTAAGAAA	154214
rs755680443	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124965837	CCTGCTTTTTATTTT[-/C]TCCATAGCACTAACA	154214
rs755703493	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058160	ATCTGGATGTGACTG[A/G]ACAATATTTACATTA	154214
rs755703637	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125045034	ACATTACGTAGTGAT[C/T]ATTTTGGTATTGCCT	154214
rs755706236	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125013150	TTATAAACTGTTCAT[C/G]GTTCTGGGGATATAG	154214
rs755711544	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965701	AGGAAGGTTCCCTCC[A/G]TGGCCCTCTTATCTG	154214
rs755728379	in-del	-/TTG			intron-variant	RNF217	GRCh38.p7	6:125027467	GCAATTTCCTCCATA[-/TTG]TTGCAAGTGACAGGA	154214
rs755736895	snp	A/G	2.46807e-05	0.0035128	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963003	CGTGCTGGGTCAGCG[A/G]CGCCCGTCCCTCGCC	154214
rs755758048	snp	A/C	0.000113617	0.00753629	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963088	CCCGCCTCGGAGCAG[A/C]TCTCGCCGCCCGCGT	154214
rs755796003	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124999244	ATGTCATTCCATTTT[G/T]AATCTGCCCGTGTCA	154214
rs755797189	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125075401	GTTTAATTGACTCAT[C/G]GTTCCGCATGCCTGG	154214
rs755803521	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049579	TGAGTATCGTTTCCA[C/T]GTCTTTAACTGGGGA	154214
rs755810787	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091299	CTTTGTGTGATGAGT[A/G]TATAACATTCATATA	154214
rs755824941	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125031290	TTTACTCATGATCTT[C/G]GGGATTAACATTAGG	154214
rs755862359	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026807	GAAATCTGCCCAAAT[C/T]ATCTCCCTTACTGGA	154214
rs755863392	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004374	TATGCCCTTACCCTT[A/G]GATTGTACCAGCACT	154214
rs755883213	snp	A/C	0.000141894	0.00842182	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971520	GAGTGCAGTGGCATG[A/C]TCTCGGCTCACGGAA	154214
rs755915670	snp	A/G	1.64955e-05	0.00287184	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076832	AGAGACCTCATTTAA[A/G]GAGATTAGTGCGAGG	154214
rs755948052	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125080208	TTTAAGAGTGTACTA[A/C]ACGTAATTATTCAAT	154214
rs755962968	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081605	CAGTTATTAAGTGGA[C/T]ATAATTTATGTTGTA	154214
rs755999255	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124993455	GTTTTCCTTTCTTTG[A/T]TGAAGAGGCTTAGGA	154214
rs756066638	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124978971	GGGGAATGCAAGCTG[A/T]TTGGTCCATGGGTGG	154214
rs756066644	in-del	-/AGATAGGT			intron-variant	RNF217	GRCh38.p7	6:125074291	AGGTCGGTAGACAGA[-/AGATAGGT]AGATAGATAGATAGA	154214
rs756089521	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124975245	CCACAGCTTTTCCCC[C/T]GGTTGCTTAACAATT	154214
rs756130744	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125054126	GAACTTGTGGGCTGT[G/T]GGAGAGATTAGACAT	154214
rs756139809	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125040030	ACCCTAACATCACAA[C/G]TGTAGAGAAGCAAGA	154214
rs756146699	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125065592	GTTATAGATGATGAG[C/G]GCTTCTGCAAAGGAT	154214
rs756157360	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084377	TATGATATGCCTTTG[C/T]TTTCATCACAAAAGT	154214
rs756176528	snp	A/C/G/T	5.24999e-05	0.00512327	intron-variant	RNF217	GRCh38.p7	6:125057923	CACTAGTAATTAATA[A/C/G/T]GATTTTTTTCTTACA	154214
rs756178429	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978718	GGTGCCTGCAGCTCA[A/G]TGAATGAGAGGGTTA	154214
rs756223596	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995384	GATTTTATTGAATTA[C/T]TTATTAATTTAGTTT	154214
rs756233372	snp	C/T	3.91765e-05	0.00442569	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082964	TTTCATCCAGCTAAG[C/T]TGGTTGGAGTAGGAG	154214
rs756247343	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125071678	TTATTCTGAACATTT[A/C]ATCTTATGACCTTAA	154214
rs756264440	snp	C/T	2.694e-05	0.00367005	synonymous-codon, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962769	GAGGAGCCTGGGGCC[C/T]CCGGGCTGGAGTAAG	154214
rs756266053	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125027403	ATAAGTGAGAACATG[A/C]AATGTTTGTCTTTCT	154214
rs756277835	snp	A/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982996	GAAAAGGGAAGAAGC[A/T]CATATAGGTGTCACA	154214
rs756322740	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124984434	ATGCCTGTAGTCCCA[C/G]CTACCAGGGAGACTT	154214
rs756416865	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032225	TCTCCACTACACAGT[A/G]AAGAGGGTTAGGAGA	154214
rs756451069	snp	G/T	1.67119e-05	0.00289062	stop-gained, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081474	CTAATTATGGTTTTG[G/T]GATTGGCACTAGGGG	154214
rs756521750	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988772	TTAATCTTTGCCTAT[A/G]GTTATTCCACAGAGA	154214
rs756521801	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973744	CCATCTATCACTGAG[A/G]TGTGTCTTCTTTAAT	154214
rs756530461	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124994332	GAAGCAAAATCCTGA[C/T]GTGATTTCATCTGCA	154214
rs756548834	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125076953	TAATTCAGAGCACCT[G/T]CCATGTGCCCAGTGT	154214
rs756580515	in-del	-/AGAG			intron-variant	RNF217	GRCh38.p7	6:124979043	CCAGAAGAAACCAAT[-/AGAG]AGAGAGAGTGTAAGA	154214
rs756585261	snp	A/G			synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058097	TGCCCAGAAGTGTCC[A/G]AAGTGCAAGGTGAGA	154214
rs756594081	in-del	-/ACTT			intron-variant	RNF217	GRCh38.p7	6:124994293	TATCTATTCCCACTC[-/ACTT]CCCCTTCCCTTCCTT	154214
rs756609722	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975232	GCAAGTTTAATCACC[A/G]CAGCTTTTCCCCCGG	154214
rs756636647	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125065481	GCAGGACATACATAA[A/C]TGCCAGCCCCACCAT	154214
rs756643562	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125031952	CAGTTCCGCATGTCT[G/T]GGGAGGCCTCAGAAT	154214
rs756654352	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022166	GGATTACAGGCCTGC[A/G]CCACCATGCCTGGCC	154214
rs756658478	snp	C/T	3.41839e-05	0.0041341	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048231	CACCCTGTACTGAGA[C/T]TAAGATCTTTGTTCT	154214
rs756659924	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125007314	GCAGTGGTGCGATCT[C/T]GGCTCACCGCAACCT	154214
rs756673850	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124992074	AACATTGCAAATTCT[A/G]ATTTACTAAGCCTGA	154214
rs756684544	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125053152	CATTCTCTCTGAACG[C/G]TTATGTTCCAGCTTC	154214
rs756704293	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125007406	ATGCGCCACCAAGCC[C/T]GGCTAATTTTTTGTA	154214
rs756707054	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083497	GGGAATGAGTGAAAC[C/T]AAATTAATGAGAAGA	154214
rs756712017	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987453	TAGAATTGCTTTTCC[C/T]GGACATTTTATATAA	154214
rs756758313	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067780	TCAGTAGAGATAAAG[A/G]TCTACCTTTGTTGGA	154214
rs756783537	snp	A/C	0.00042732	0.0146109	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963101	AGCTCTCGCCGCCCG[A/C]GTCGCCACCTGGGGC	154214
rs756800677	snp	C/T	0.000284131	0.0119157	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971524	GCAGTGGCATGATCT[C/T]GGCTCACGGAAACCT	154214
rs756803420	snp	G/T	1.6504e-05	0.00287258	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076713	CTCACAATGTAACAC[G/T]AATTTTTGTTACCGA	154214
rs756808348	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125038816	TTTTTTTGGGTGTAT[C/T]AATGATCTTTTTTTC	154214
rs756822381	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125010477	AATAGCTCAAAGGAG[C/G]ATTGTGTTTGGCAGA	154214
rs756831864	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125010934	CAGTTAAGATGTACC[G/T]TCAAAAAGACGGGGT	154214
rs756850555	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068629	CATAGCTTATGCATA[C/T]ATATTTGTTTATACA	154214
rs756862904	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024840	AGTAGGGAATTAAAC[A/G]TAGATATCAGAAGCT	154214
rs756877551	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125055129	CAATTTCAGATGTAG[A/T]CTTTTAATACCAAAG	154214
rs756898690	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057036	GGCCACTATATTGAT[A/G]TATTTCTAATAATAG	154214
rs756947975	snp	A/G	5.9961e-05	0.00547512	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082970	CCAGCTAAGCTGGTT[A/G]GAGTAGGAGCGATAC	154214
rs756964599	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125060382	CACACACACACACAT[-/AT]ATATATTTGTACCCT	154214
rs756965815	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124979894	TTGCACTAGTGTACA[A/T]GTGGTGGAGATGGCT	154214
rs756967838	snp	A/G			intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124964164	GACCAGCTTTCCTTC[A/G]CTGACGGTGAATGCG	154214
rs757012112	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984361	ACAGCAACCCGGGCA[A/G]CATAGAGAAACCCTG	154214
rs757046755	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125013385	GTGTGTGTGTGTGTG[-/C]TGTGCTGTTTTTGAG	154214
rs757064701	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026563	GTCATCAGTACTCCA[C/T]ATTTCTGTGTAGAAA	154214
rs757133491	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002576	AATTTTTTTAACCTT[A/G]TTATCTACGACCACA	154214
rs757148181	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003833	AGCTTCTTATATGCT[A/G]TGTCTTGTAGTCCTC	154214
rs757191867	snp	C/T	1.80016e-05	0.00300008	intron-variant	RNF217	GRCh38.p7	6:125081419	CTCCTTAAATAATTT[C/T]GCCTTTTGTTTTCCA	154214
rs757200524	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049371	AAGTTTACTTCATTT[A/G]CTGCTGATAACCTGT	154214
rs757238591	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125079907	AGAGATAGTATGCCT[A/G]GTCCCTTAAAACAGT	154214
rs757292959	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973338	TTATATCACCACCTG[A/G]GTTAGTCCTGCTGTT	154214
rs757314047	snp	G/T	1.80991e-05	0.00300819	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962864	CACTGCAGTTGGAGC[G/T]GGAGGAGGAAGAGGA	154214
rs757315711	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001200	ATTGGAGTTAGTTAT[A/G]TTAGGGAATGCTGAA	154214
rs757315971	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125051299	GTCATTGGGTCTTTA[G/T]CACAATGAACAAGTG	154214
rs757325037	in-del	-/C	5.65105e-05	0.00531527	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962925	GAACAGCAGGAGGCG[-/C]CCCCCCGGCGAAGAG	154214
rs757343349	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125007348	CCTCCTGGGTTCAAG[C/T]GACTCTCCTGCCTCA	154214
rs757381683	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021141	AAGTTATTCATCCCA[C/T]ATTATTTATAATAGC	154214
rs757382476	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083047	GGAACCTTCTACCAT[C/T]TCATCTCCCAGTGAT	154214
rs757403705	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040306	CCATCAGAGAATACT[A/G]TAACACCTCTACACA	154214
rs757411820	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053004	CTCTGTTCAGGCTAC[A/G]TTAGAACACTTGCTG	154214
rs757425110	in-del	-/TTAAGT			intron-variant	RNF217	GRCh38.p7	6:125010591	TCAGTTTAAACAAGC[-/TTAAGT]TTATTTTATGCAATA	154214
rs757441554	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026412	GAATAGTGCCTGGCA[C/T]ATACTAAACGCTCAA	154214
rs757464087	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125013719	ACTCCATATATATCA[A/G]TTACATCCCAGTCAT	154214
rs757501753	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125041462	TTTTACCATGGCCAA[A/C]AAGGCCCATGTGATC	154214
rs757545607	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089463	TATAAGATTCAATTA[C/T]GGATTCATGCTCTGT	154214
rs757548307	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044865	CCCGCAGTTCTTGCA[A/G]TTGGTGCATCATCTG	154214
rs757551132	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084217	CACCTTCTTATGGAG[A/G]AGTTTGAAAACTTTT	154214
rs757562848	snp	A/G	3.94205e-05	0.00443945	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048254	TTTGTTCTTTGTGAT[A/G]AACAGGTGAACATTT	154214
rs757567772	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075826	GGATTCTGAGTTGAG[C/T]TTCCAATTTTATCGC	154214
rs757601408	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124986326	TCCTCCCACATCAAG[A/C]AAGTTTTGTGGTTAG	154214
rs757606869	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125070664	GAGAAATGTCTATTC[A/G]TGTCCTTTGTCCACT	154214
rs757615422	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040588	TCCGTAACTCATTTT[A/G]TGATGCCAGCATCAT	154214
rs757656807	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125063013	TTAGTTATCTTAGTT[A/G]TCACAAAAATAAATC	154214
rs757667887	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999123	GCATACTAGGAAAAA[C/T]ATACTGTGTATTATA	154214
rs757668060	in-del	-/TG			intron-variant	RNF217	GRCh38.p7	6:124998792	AACAGAGCGAGACTC[-/TG]TCTCAAAAAACAAAA	154214
rs757730845	snp	A/G	1.74934e-05	0.00295743	intron-variant	RNF217	GRCh38.p7	6:125057924	ACTAGTAATTAATAT[A/G]ATTTTTTTCTTACAC	154214
rs757740116	snp	A/G	4.53566e-05	0.00476196	intron-variant	RNF217	GRCh38.p7	6:125082428	CATTATGTAATAGAT[A/G]TTATTATCTGTATTA	154214
rs757747683	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987881	AACTTGTACATTCTG[C/T]GGTTTGTTGTGATTT	154214
rs757752805	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124994144	AAAAAAAAATATGTA[C/T]ATAAGGGATGTGTGT	154214
rs757762154	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125059147	AATATAGTAAGGAAA[-/A]GTATTGTATGAAATA	154214
rs757787401	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125054092	CAAAGCCTTTGACAA[-/AC]ACAGTTCACTGAGGA	154214
rs757796864	snp	A/G	2.45269e-05	0.00350184	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962773	AGCCTGGGGCCCCCG[A/G]GCTGGAGTAAGAGCC	154214
rs757824649	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125064286	TCACTAAATCTGGAG[C/T]AGGGGTTATCATTGG	154214
rs757862581	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125019653	TTCCACCAAATTAGA[C/T]GAATAATTTAGTTTC	154214
rs757892762	snp	G/T	3.29821e-05	0.00406078	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009322	ACATTTATTTGTGCT[G/T]CAGGAGCCCTTGTAA	154214
rs757910925	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078470	GCTGAGCAGTCCAAG[A/G]TGTAGTGGCTGCATC	154214
rs757933806	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091727	TGTATGGTACTTCAG[A/G]AATTTGACCAGTTCC	154214
rs757946255	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125002411	TTCTGCTTCCATTTC[C/T]GTATCCAAATGCTGT	154214
rs757992582	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037775	ATTGTTACTGCTTTC[A/G]TTGCAATATTCTCTT	154214
rs758002947	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125003113	CACACGCACACAAAC[-/AC]ACACACACACACACA	154214
rs758020889	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125066369	CCCTCTGGACATGTC[C/G]CCACTCTGTGACTCC	154214
rs758034241	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990785	AAGAGTGAAGCCAAA[C/T]TGGGCATGGTGGCTT	154214
rs758034757	snp	A/G	3.33111e-05	0.00408099	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125057962	GTGCCCTACCTGCCA[A/G]TTCGTCTGGTGTTTT	154214
rs758053537	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124977171	AAAATAATATAAAAC[A/G]TTAACACTTTCTGAC	154214
rs758123955	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044033	TGCCAGATAAATAGC[A/G]ATGTTAAAAGTTACT	154214
rs758148162	snp	A/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981440	TGAGACATCAATCAG[A/T]ATGTGACCAAACATT	154214
rs758263392	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058362	GACATTGAGGTCCTT[A/G]TATTACATTTAAAAA	154214
rs758267394	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071398	CAGCATTTTTTGGAT[A/G]TTGTGTTTTGTTTTT	154214
rs758271190	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124984616	ATAAAGGTGCAAGGA[C/T]GGTAGGCTTTCCATA	154214
rs758282504	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125015049	CCATTTAGCTACTTA[C/T]TTCATGTCTGAAGTA	154214
rs758315906	in-del	ATATATA/GTGTGTGTGTGTG			intron-variant	RNF217	GRCh38.p7	6:125071524	TGTGTGTGTGTGTGT[ATATATA/GTGTGTGTGTGTG]TATATCTTATTACAG	154214
rs758326270	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968331	TTCTGTGTGCAAAAT[A/G]TATGTGTGTGTGTGT	154214
rs758353403	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125059739	ATGGGGAATTTACTG[A/T]ATGTTCTAACAACTT	154214
rs758373107	snp	A/G	0.000511291	0.0159807	intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971595	CGAGTAGTTGGGACT[A/G]CAGGTGCGTGCCACC	154214
rs758388054	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077377	TAATTATTAATAGGT[A/G]ACAGTTAATATAATA	154214
rs758427041	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000643	CAGATTTGTATGCAT[A/G]TTAGAGAAATAGAGA	154214
rs758464504	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125019494	GTCTAACAATATATA[C/T]GTTATTCTTATATGA	154214
rs758501293	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124971045	GAACAATTCTGTTTT[C/T]GTACTGCAGGTAGTA	154214
rs758517551	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061973	ATCTAACCCAATTGT[A/G]TTTATGGGATGACTT	154214
rs758550473	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125005937	TAAAAATCATTTATA[C/T]TGTGCCAGCCTTGAG	154214
rs758559087	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004479	TAAGCAGAACAGTGA[A/G]GATCCTAGCCCTGGG	154214
rs758561895	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125063918	GATATTTTATTCTCT[G/T]CAATCCTATAATAGA	154214
rs758600038	in-del	-/AAATATGGGGCCATGT			intron-variant	RNF217	GRCh38.p7	6:124978175	TAAAGCTCTCCAGGC[-/AAATATGGGGCCATGT]ATATGAATAAATTGT	154214
rs758621588	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124978622	CCCATAGTCTGACAA[A/G]CGGGAGTGTGCTGCA	154214
rs758643139	snp	A/G	1.6528e-05	0.00287467	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045294	TGTTGTCTATAACTT[A/G]ACGCATGAAGACTCC	154214
rs758684992	snp	C/T	5.7474e-05	0.00536038	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962798	AGAGCCGAGCACCGG[C/T]GCAGCCTGCGGGACT	154214
rs758685787	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973000	CACTTTGTGTGTTAT[A/G]TATACTCTATAAGTA	154214
rs758703215	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086478	TATCCACTTTTGTGT[A/G]TGTTGCTTGACAGAG	154214
rs758732962	snp	A/C	1.78052e-05	0.00298367	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045432	CCCTTCCAGATCAGA[A/C]AGCAAATACAAAGTA	154214
rs758733350	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125038136	AATGATGCCTTGTAG[A/T]TTCCTTTAGAGTTAA	154214
rs758734298	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125010828	GTAGCAGAGAGAGCT[A/G]AGGAATGATCTAAGG	154214
rs758749314	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125062965	TAAATTCTTAACCTA[G/T]GGAAAATATGTGCTA	154214
rs758752061	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124997528	TCACTCATAGCTGTA[C/G]TAATGACAGCAGACA	154214
rs758824204	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011879	TAATAACTGCCAGCC[C/T]TAGTTTTTGGTGCTG	154214
rs758824859	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125043023	AAAACTGCAGTTTTC[G/T]ATTTAAATAGAAAAA	154214
rs758828667	snp	C/T	1.65663e-05	0.002878	intron-variant, synonymous-codon	RNF217	GRCh38.p7	6:125082549	AAGTGATATGCTATA[C/T]TGCCTGAAACAAGTG	154214
rs758830005	snp	C/T	1.65373e-05	0.00287548	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058058	GCGTCACTGGGCCAG[C/T]GAAATTGAGCATGGG	154214
rs758837719	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125021071	AGATACTTTAACCCA[A/G]TATTTTCAGTTCTGG	154214
rs758847605	snp	G/T	0.000149154	0.0086345	missense, synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125082864	TTTTCTTATCCCTAG[G/T]TTTATTTGTATTTCC	154214
rs758882944	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125017005	CCATGGGATACTACG[G/T]AGCCATGAAAAGGAA	154214
rs758899426	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087513	CACTTTAAAATATTT[A/G]TGCCATTTAAATAAT	154214
rs758909361	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125043866	ATGCAACAATTTATA[C/G]TTTTAACAGGTCAAT	154214
rs758917714	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125073571	AGATAAGGCAACCCA[C/T]AGCAAGAAACATGAG	154214
rs758953124	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074202	ATGAAGTGCCCGCCT[A/G]TAATATGCTGTGTTC	154214
rs758953256	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124988951	AATTGCATGTTAATG[G/T]TGCTTCCAAGTTTTG	154214
rs758993664	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125030400	CCAAAATCCCATCTG[A/T]GACAAGGCAACTCCC	154214
rs758997499	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044773	TGTGCCCAGAGTTTA[A/G]TGCTGAAGTATTCTG	154214
rs759045658	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125027954	TTTATTCAAATCATT[C/G]CCCATTTTTTAATCA	154214
rs759063238	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124993619	CTATTCGGGTAGATA[C/T]ATAAGTAAAATCACC	154214
rs759067574	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124984030	ATCCTGTTTATTAGG[G/T]TAGAGCCCTCCATCA	154214
rs759078858	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124969428	GAACCTTCCCAAATT[A/G]AATTTTTGCTTTAAA	154214
rs759081560	snp	G/T	1.67685e-05	0.00289551	intron-variant	RNF217	GRCh38.p7	6:125082613	GACAATAAAGAAGAT[G/T]TAAACCAAAGTTTTG	154214
rs759135787	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049076	TTCTACAAGGTTGAC[A/G]TCAGCTTCCAACTAG	154214
rs759137258	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995361	ATTCAGAGCTAAACA[A/G]TGTCCTGGATTTTAT	154214
rs759139733	snp	A/G	3.33762e-05	0.00408497	intron-variant, missense	RNF217	GRCh38.p7	6:125082494	TAAGTGGTAGAACCA[A/G]GAATCAAACCCAACA	154214
rs759212208	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125021759	AGTCATTTATCAGCT[G/T]TACAAACACAGGTGA	154214
rs759254231	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125002160	TGATGAGCCTAGCCA[G/T]GACATCTTTGTCTTG	154214
rs759268315	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017365	TAGTTGTCCTAAGCA[A/G]GGTTTTTGAATCAGC	154214
rs759291250	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124970664	GTATTTAAAGCTATT[A/T]GACTGGATGAAGTCA	154214
rs759304705	snp	C/G/T			intron-variant	RNF217	GRCh38.p7	6:125052838	TCTTTAGGACATACC[C/G/T]GAATCTGACAGCCAT	154214
rs759306905	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065927	AATAGACTTCTCCAA[C/T]GCAGTATGTTCTCTT	154214
rs759346158	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124974556	ATAATTCTGATTAAC[A/T]ACACTTAATATTATT	154214
rs759468128	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124995724	GTCAGGAGTTCGAGA[C/G]CAGCCTGACCAACAT	154214
rs759473719	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979552	CAAGTGTGCAAAGCC[C/T]GGGGTGGGCATAGGC	154214
rs759482107	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011747	TTATTTCTTTCATGG[A/G]ATTTTCCCATCTAGT	154214
rs759504670	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124984166	TTTTATAGGTACAAA[C/T]AAATTACTGGAACAG	154214
rs759518010	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009762	AAGCTGCATTCCATC[C/T]CCGTGCACATTCGTT	154214
rs759527179	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124991039	ACCACTGCAAAGCCT[-/G]GGTGACACAGTGAAG	154214
rs759532370	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042349	ACTCATATCCATTGT[C/T]CCAGAAATAGATTCA	154214
rs759551849	snp	A/G			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963697	CTCCTCTTATTTCTT[A/G]TACAGGATTGCAAGC	154214
rs759553140	snp	A/G	1.65455e-05	0.00287619	synonymous-codon, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045249	CAAATGCCCCATCAC[A/G]GAGTGTTTTGAATTC	154214
rs759558978	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125071273	AATTTTGAATTTCGA[C/T]CTTTTCCCAGGCTCA	154214
rs759562178	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125025246	GGAGGAGGTGAGACA[G/T]ATAGCAGTGGGTTTT	154214
rs759570078	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998352	TGCTGTGGGATATGG[A/G]CAAGGGGAAGTGAAG	154214
rs759589181	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085452	GAATTTTTTACTAAG[C/T]TTCATCAAGATCTTA	154214
rs759673004	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125056554	AATTACAGTGCTTTG[-/A]GTTATTAACAGAAGA	154214
rs759710898	snp	G/T	1.75471e-05	0.00296197	intron-variant	RNF217	GRCh38.p7	6:125057917	TATATCCACTAGTAA[G/T]TAATATGATTTTTTT	154214
rs759712604	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012697	CAGACAGCCTTGGGA[A/G]TTAAAGTTATATTTT	154214
rs759720820	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987847	ATATTAGTTGTTACA[A/G]TGATTTTACTGCAAT	154214
rs759727285	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088014	TAAGTTACAAAATTC[-/T]TTTTTTTTTTTTTTT	154214
rs759752023	snp	G/T	7.66871e-05	0.00619174	intron-variant	RNF217	GRCh38.p7	6:125081393	AATTATTTGGTAGGT[G/T]AGTTTTAAGACTCCT	154214
rs759815923	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125031027	TGACTTCTTTGCACA[C/T]GCACGCGGAACACCA	154214
rs759849189	snp	A/G	3.29815e-05	0.00406075	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076786	ACATCAAACCTCAGT[A/G]TATTTGGATGCAAAT	154214
rs759849715	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062641	GAGTGCAGTGGTGCT[A/G]TCTCGGCTCACTGCA	154214
rs759853271	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045544	GGCATCTTTCCTTTA[C/T]GGAGCTGAAGGTGAG	154214
rs759854041	in-del	-/AA			intron-variant, upstream-variant-2KB, frameshift-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964007	AAGCCAGCACTCTTT[-/AA]AAGAGGGAAGCAAAA	154214
rs759905053	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125080885	TTATTCATAGTTTTC[G/T]CTAACATCTTGAAAC	154214
rs759933273	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003259	TCGAGAGGCTGTATG[A/G]TTGTACAATCACTGA	154214
rs759940900	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125079338	AAGTTTTAAATCAAG[A/T]CGTATAATTTTTAAG	154214
rs759950124	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124992978	TTCCAATGTAATAGA[A/G]TATTTGTTCATTTTA	154214
rs760038526	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024626	GGGAGGCTGAGGCAC[A/G]AGAGAATCTCTTGAG	154214
rs760038578	snp	A/C/G/T	5.78001e-05	0.00537564	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082957	CAGATGATTTCATCC[A/C/G/T]GCTAAGCTGGTTGGA	154214
rs760064075	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067202	TGTGGTTAACTTAGC[A/G]TAAGGTTTATGCAAG	154214
rs760099244	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083817	AGGAGTATTAAGCTT[A/T]GTAAACTGACAAAAC	154214
rs760137249	in-del	-/TTT			intron-variant	RNF217	GRCh38.p7	6:125064902	AACCATGCAAACATA[-/TTT]TGGACTTACATATAA	154214
rs760145893	snp	A/C	0.000830082	0.0203556	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963304	GGCGGTGTAGGGGAT[A/C]CCTATGTGCCCCTCA	154214
rs760154048	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125054788	CTTGTGAAAATGTGC[A/C]CTTTTGGCTCTGAGG	154214
rs760171708	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994666	CTGCTTTTTGTATAT[A/G]TCCTCAAACTACTAC	154214
rs760183464	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125016091	GAAGAAGAAATGAGA[A/C]TATAAGGGGGAAAGG	154214
rs760183825	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042851	AATAAAATAAACTCA[C/T]AGGTGAAGAAGGCTG	154214
rs760217743	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982131	TTTATTTTTGTAGCT[A/G]TCTTATTTAGGAATA	154214
rs760233873	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041174	TATTAAAACATCATG[C/T]TGTATACCATAAATA	154214
rs760296706	snp	A/C	9.9054e-05	0.00703685	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962732	ACTGGGGCTGCGCGG[A/C]CACCAGCGCCCCAGA	154214
rs760321373	snp	A/C/G	3.66235e-05	0.0042791	stop-gained, missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082934	GACAGGTATGCACTG[A/C/G]TAACATGCAGATGAT	154214
rs760321573	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042250	TGTTCCAAACTGCCA[A/G]TTACTGGCTTGTCAA	154214
rs760344685	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125031723	AGTCTCTAGGAAGTT[C/T]CAAACTTTCCCACAT	154214
rs760377176	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125063693	ATAACATAACAGGAT[C/T]GGTAGTATGTAAGTT	154214
rs760411538	snp	C/T	2.03209e-05	0.00318748	intron-variant	RNF217	GRCh38.p7	6:125082824	AGGAAAACCTAAATG[C/T]CTCTCATCCTAACTA	154214
rs760418604	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125019376	TTCTTACCATTTTAC[C/T]CACCTCCATCCATCC	154214
rs760464413	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076934	TGGAAATGTGCAGCC[A/G]TGGTAATTCAGAGCA	154214
rs760467080	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050937	AGCCCTGTTGATAGA[C/T]GCCAGTGTAAACAAA	154214
rs760475031	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987586	TTGAGCTCAGAAAAT[A/G]TGTCTACTGCAAATT	154214
rs760480801	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054119	GAGGAGTGAACTTGT[A/G]GGCTGTTGGAGAGAT	154214
rs760482355	snp	A/T	7.56158e-05	0.00614835	intron-variant	RNF217	GRCh38.p7	6:125081405	GGTTAGTTTTAAGAC[A/T]CCTTAAATAATTTTG	154214
rs760505494	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125037522	TGATTTTTTAAATCA[-/T]TTTTAGAAAAATTCA	154214
rs760548152	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029748	AAGAAATGATCTTGT[C/T]ATTATATCTGTTAAG	154214
rs760565011	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988151	GGATCTGGGTTGCAC[A/G]CTCCTTATGAGAATC	154214
rs760566645	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972665	TACCTTTAGTGATAT[A/G]AAGTTCTGTCTTAGG	154214
rs760568845	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057560	CCATTCTTAAGAAGA[C/T]AATGGAAATGGCTGG	154214
rs760630038	snp	G/T	1.67626e-05	0.002895	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045404	CCTTCAAGAAAAAAG[G/T]ACATATTCCCACCCC	154214
rs760651906	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125079438	AATGAATACTCAATT[-/A]AAAAAAAAAAAAAAA	154214
rs760678130	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991438	CTACCAACCCTCATC[C/T]CCCCCATACCAGCAT	154214
rs760702909	in-del	-/TAAG	3.41279e-05	0.00413072	intron-variant, frameshift-variant	RNF217	GRCh38.p7	6:125082478	CTTACTGGAACCTCA[-/TAAG]TAAGTGGTAGAACCA	154214
rs760724001	snp	C/T	7.11238e-05	0.00596295	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048191	CCCCAGCCAACCAAT[C/T]GTGAGATTCATGGCC	154214
rs760770752	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125055315	CCCACTAAGTCTGTG[-/C]TGTTGGTGAGGATTT	154214
rs760778618	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124978137	CAGCTTCTTAGAAAC[G/T]TTAGAGCTTTAGTAG	154214
rs760823774	snp	A/C	1.68083e-05	0.00289894	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081503	GGCCATAGCGGTTGT[A/C]ATCGGTAAGAAACAC	154214
rs760825394	snp	A/C	1.65149e-05	0.00287353	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058023	AACTGCAAGGAGTAC[A/C]AAAAAGGAGACAAAT	154214
rs760850050	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124983682	GCTATATTTCAAATG[C/T]AGTATTTTCTTACTG	154214
rs760861706	in-del	-/TT			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009642	CCTGCCCTTCCTTCC[-/TT]TTTTCTTTCTATTTT	154214
rs760862519	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964634	CAAAGACTTAAAACG[A/G]TATGTTACATAAACA	154214
rs760885553	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125010378	ATGTGCTTTTTAGGT[A/G]TAATGCATGAAGTGA	154214
rs760915345	snp	A/T	1.81013e-05	0.00300838	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962855	AGACCTTGCCACTGC[A/T]GTTGGAGCTGGAGGA	154214
rs760932991	snp	A/T			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963496	GTCCTGCTCTCGATC[A/T]GATCTCCCTGCTCGC	154214
rs760934272	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125047940	TACTCTTCTTTACTA[A/G]TGTAGAAGAGAAGAT	154214
rs760949421	snp	C/T			downstream-variant-500B	RNF217	GRCh38.p7	6:125092824	TGTGTTGCTGTGGCA[C/T]GTTTTGGGGAAAGAG	154214
rs760970166	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125043409	CCCAGGTCTGAGATT[A/G]CTATACTTCTCCTGA	154214
rs760995771	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125045972	AGATGGGAGAGACAT[G/T]TGTTCTAAAAATGAC	154214
rs761009178	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125060961	TCATTACTATTTTCA[C/T]CTAACATTGCAAACA	154214
rs761071532	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003122	CACAAACACACACAC[A/G]CACACATACCTATTC	154214
rs761085449	snp	C/T	0.000111838	0.00747707	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963403	GTGTGCGAGGAGTGC[C/T]TCAAAGTCTACCTGA	154214
rs761096207	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037366	AGGCTGAAGTTTTCT[A/G]CTTGGGAATATGCCT	154214
rs761099230	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125049052	TGCCAGAAAGGCTTA[A/C]CGTTCCATTTCTACA	154214
rs761138497	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125002058	TATGAGCCCCAAACT[C/T]CTAATGGATGGTATG	154214
rs761213315	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078021	TTTTCTAAAATCTAT[A/G]TGATCTCTATAAAAA	154214
rs761231978	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061514	TTGGGGCATATTTTT[A/G]TTATCAAATTTTATG	154214
rs761269881	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006888	CAGGAGGCAGAGGTT[A/G]CAATGAGCCGAGATC	154214
rs761342399	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125037634	AATCACTGATGAGTA[A/C]AGTGAGGCGGACATC	154214
rs761382801	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125050685	AGCTTTCCCATGAAC[A/G]TGTAATGAGTATGCT	154214
rs761425002	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124993403	TTTCCACTAAAATTA[G/T]TATCATTAGCCCATC	154214
rs761499043	snp	C/G	3.48183e-05	0.00417228	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048200	ACCAATCGTGAGATT[C/G]ATGGCCACAGTATGG	154214
rs761504984	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:124988172	TATGAGAATCTAATG[-/C]CTGATGATCTGAAAT	154214
rs761566852	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041042	CTGGCACAAGACAAG[A/G]ATGCTCTCTCTCACC	154214
rs761569205	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030132	TTGTGAGACTTATTC[A/G]CTATCACAAGAATAG	154214
rs761640680	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998053	GATGCCTCAGATTAT[A/G]TATGTTCAGAGCAAA	154214
rs761651081	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125030907	CACTGCCCTAGCAGA[C/G]GTTCTACATGAGGGC	154214
rs761784008	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125057037	CCACTATATTGATAT[-/C]ATTTCTAATAATAGA	154214
rs761784883	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125029329	TTTATTTTTTCATAT[A/T]CAAATACACTTTGAT	154214
rs761814689	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988436	TCATGACAGAATTCA[C/T]AGAATGATTGTTAAA	154214
rs761821013	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125001844	TTCAAAGCAAAGATA[A/C]GTGAAAAAATGCATA	154214
rs761863731	in-del	-/AC			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961015	GCAACTGAGCCTCAG[-/AC]ACACATATATGATGG	154214
rs761865487	snp	A/C	1.80062e-05	0.00300046	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962737	GGCTGCGCGGACACC[A/C]GCGCCCCAGAGCCCG	154214
rs761872456	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972555	GACTCCTGTGTGTCC[A/G]TCTGAGCTTTCTTTC	154214
rs761911003	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124990159	CCATAGTCTTCATTT[G/T]CTTCATTCCACACTG	154214
rs761937997	snp	C/T	1.67553e-05	0.00289437	intron-variant	RNF217	GRCh38.p7	6:125076629	TCAGCTAACTCTTTC[C/T]TTCTCCTTCCCTCTC	154214
rs761955920	snp	G/T	2.12307e-05	0.00325806	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962968	ACCCGCGTGGGGGCC[G/T]CCGACGGACTGGTCC	154214
rs762001966	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092345	AGTCTAATTTCCGAC[-/T]TTTCGTAATGTCCCA	154214
rs762043790	snp	A/G	0.000222321	0.0105409	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963040	CAAGTCTTCTGCTCC[A/G]TGTACTGCGTGGAGA	154214
rs762044753	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125013009	AGAAAGTTAGCATTT[C/G]TATCTTGATTCTTCT	154214
rs762047089	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022103	GGCCAGGCTGCTCTC[A/G]AACTCCTTACCTTAG	154214
rs762053828	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125053892	TTTGTGCGTTGATCA[A/T]AGTGCTTAGTAAAAG	154214
rs762064522	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976766	TGCCTGGGCCTCCCA[A/G]AGTGCTGGGATTACA	154214
rs762086326	in-del	-/T	3.34174e-05	0.00408749	frameshift-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081477	ATTATGGTTTTGGGA[-/T]TGGCACTAGGGGCCA	154214
rs762100771	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125008527	AGGCCTTGGTTTCCA[A/G]CTTCTTGGAGTGATT	154214
rs762113903	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125020182	TGGCTTGGGCTCAGA[C/T]GTCTGCCAAGGTCTT	154214
rs762144212	snp	C/T	8.40273e-05	0.00648125	intron-variant	RNF217	GRCh38.p7	6:125045206	TCTGCTCTTCCATCA[C/T]GCAGGTACAACTTGG	154214
rs762150629	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071128	AACAACTTGAGGAGG[A/G]CAGGTACTATTTTCT	154214
rs762204628	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125069617	GCTGCAATGAAAATG[C/T]AAGTGCATCTTTTTC	154214
rs762240062	in-del	-/AGTG			intron-variant	RNF217	GRCh38.p7	6:125069598	TTTGCTATTGTGAAT[-/AGTG]AGTGCTGCAATGAAA	154214
rs762265323	snp	C/T	1.65282e-05	0.00287469	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058044	GGAGACAAATTGTTG[C/T]GTCACTGGGCCAGCG	154214
rs762273322	snp	C/T	1.66183e-05	0.00288251	intron-variant	RNF217	GRCh38.p7	6:125076639	CTTTCCTTCTCCTTC[C/T]CTCTCTTGCTGATAC	154214
rs762289038	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014338	TCTAAATGCCTTGCA[C/T]GGATTAGCTCACCAC	154214
rs762292226	in-del	-/TG			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968335	TGTGCAAAATGTATG[-/TG]TGTGTGTGTGTGTGC	154214
rs762296813	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125045016	CTATAAGTCATTTCA[A/G]AAACATTACGTAGTG	154214
rs762300510	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124966634	AAGAGTCCCTATTAA[A/G]CATTTTATGCCAACA	154214
rs762365467	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125024825	TGACTGAAGACATCA[A/G]GTAGGGAATTAAACG	154214
rs762389816	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124969679	AGGCACTGTTTTAGG[C/T]TCTGGGGATACAAGA	154214
rs762392472	snp	C/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967398	TTTCTTTTATGATTT[C/G]GTTTAGACAGAAAAA	154214
rs762422859	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019253	ATCTGTTTTTCAATC[A/G]TAGCTATTTATTTTG	154214
rs762466946	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985328	TGCGGATACATAATA[A/G]GTATGTATATTTATG	154214
rs762483382	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124971085	ATGAGGGAACTCGAG[A/G]TTAGAGAGATTAAAT	154214
rs762484933	snp	G/T	1.70327e-05	0.00291823	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081535	TCATGCATCTGAGAT[G/T]AGAATTATCTGAGGG	154214
rs762489277	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125017612	TCTGCACTTGATACT[A/T]GGATTATCTGTTCTA	154214
rs762528331	snp	A/G/T	9.97812e-05	0.0070627	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045224	AGGTACAACTTGGCC[A/G/T]AGTAGAAATCAAATG	154214
rs762535430	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125038684	TGCTAGAAGACTATC[A/G]ATGCCAATTTAATTG	154214
rs762537637	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062370	TATAATTGTATTTTG[A/G]CAGGTAATCAGGATG	154214
rs762549573	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125034764	GATGGGGATGGCAAC[-/AT]TGAATCTATAAATTA	154214
rs762550829	in-del	-/TTAC			intron-variant	RNF217	GRCh38.p7	6:124969188	AAAGTTATAAATCTA[-/TTAC]TTATTTCTTAATATA	154214
rs762557882	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125069968	TATCCGAGCAGTGTA[-/C]ACTGTACCCATTACA	154214
rs762617719	snp	A/C	1.65529e-05	0.00287683	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045359	TTGATTCCAGCACCA[A/C]GCCATGTCCTCAGTG	154214
rs762636944	snp	G/T	1.78074e-05	0.00298385	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962752	AGCGCCCCAGAGCCC[G/T]CGAGGAGCCTGGGGC	154214
rs762638012	snp	A/G			splice-acceptor-variant	RNF217	GRCh38.p7	6:125081435	GCCTTTTGTTTTCCA[A/G]CTGGAAAATTATTCA	154214
rs762655408	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085583	TAAAAAGAAGCGTGC[A/T]CATAAAATAAATATC	154214
rs762661269	snp	A/C			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963039	ACAAGTCTTCTGCTC[A/C]GTGTACTGCGTGGAG	154214
rs762690586	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125004895	TGCTGCTATAACAGA[A/T]TACCACAGACTGGGT	154214
rs762692496	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991850	GCAACTTTTAAGGGC[C/T]CTTGTGTTCAGTGGC	154214
rs762698040	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997104	TTATTTTCTGTTTTG[A/G]TCCGGTGTGTATTCA	154214
rs762713484	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042653	GTTTGATTGGATGTT[A/G]GATGGTATCCCGATG	154214
rs762795462	snp	A/G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092572	TGTTTACCACATGAT[A/G/T]TGTGCAATACATCAT	154214
rs762801398	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125043289	TTGCCCAAGTTGTCT[C/T]TTTCATCTGCTTGAA	154214
rs762824640	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125008990	TTCCCCTGGTTTAAT[A/G]GTTGAAAATGATATA	154214
rs762875854	snp	C/G	1.82324e-05	0.00301925	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962824	GGACTGGCACTCACC[C/G]GGCCTCTCAATCCCC	154214
rs762890849	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089230	GCCTAATAATAGTCT[A/G]AAACCAAGCTTCAGA	154214
rs762893291	in-del	-/CTAA	1.70033e-05	0.00291571	intron-variant	RNF217	GRCh38.p7	6:125076618	TTTTTAAAAACTCAG[-/CTAA]CTCTTTCCTTCTCCT	154214
rs762895116	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124998982	CTTTTGTTGCCACTT[A/T]TTGTTTTCAAAAATA	154214
rs762938070	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075595	TGATCCAATTCCCTC[C/T]ACTTGACCCTGCCCT	154214
rs762971726	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014115	GTTTGCTTAGACAAC[C/T]TCAGGTAGCACCATT	154214
rs762989526	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124987824	AACACTTGAATCTTG[A/T]GATTCAAATATTAGT	154214
rs763012202	snp	C/T	0.000165248	0.00908828	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963248	CGCCCGAGCCGTTCT[C/T]CATGCCCAGCCTGTT	154214
rs763021684	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125073681	CCTATCTAGGAAAGC[A/C]CTCTCTAGTCCAGCA	154214
rs763028755	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027588	TGCTTCGAAATCTTA[A/G]CTGTTGTAAACAGAG	154214
rs763047117	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053551	AAAATAATGATGTGT[A/G]TAGGGGTATCTAGAA	154214
rs763068206	snp	C/G	7.19295e-05	0.00599663	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963064	GTGGAGAGCGACCTG[C/G]CCGAGGCCCCCGCCT	154214
rs763091948	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124989825	TCTCTTTATTGGATC[C/T]TTCTTCTTAGCATAC	154214
rs763093592	snp	C/T	1.64925e-05	0.00287158	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076770	ATTTTTTGGAGACCA[C/T]ACATCAAACCTCAGT	154214
rs763103183	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125045887	CAGAATGCTGTATAT[A/G]CTAGGCAGTGTGCTA	154214
rs763126167	in-del	-/ATAG			intron-variant	RNF217	GRCh38.p7	6:125040180	GAAAAAATTAACAAA[-/ATAG]ATAGACCACTAGCTA	154214
rs763135109	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999824	ACTTTTCACATACTT[C/T]ATACTTACTTATTTC	154214
rs763180093	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125076345	CATTTTAAATTGCCT[C/G]CTAACCGTTGAATTA	154214
rs763197053	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065042	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	154214
rs763231514	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124988234	GACCCCCATCCATGG[A/C]AGAGTTGTCTTCCAT	154214
rs763282779	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125000563	AATATTTATTATTTT[-/A]TAATTTACTAGGGTA	154214
rs763339927	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065051	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	154214
rs763340048	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089485	ATGCTCTGTGAACAT[G/T]GTTAGATTTTTAATA	154214
rs763347193	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125039817	AACCACACAACCACA[G/T]AGAAATTGAACAACC	154214
rs763352469	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993307	TCTGACTAAGCGAAC[A/G]ATATAAATAGAGTGC	154214
rs763365633	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068468	TGTCTTCATACTTTC[C/T]ACTTTTCCTTCACAG	154214
rs763398068	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979721	CTATGATGGTAAATC[C/T]TCGGACAGTTTGCTT	154214
rs763442757	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124994321	TTCCTTATTTTGAAG[C/T]AAAATCCTGACGTGA	154214
rs763458811	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012774	TGATGCTTTAATTTG[A/G]TTTGATTTTTGGCTT	154214
rs763484263	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124965200	GACACAGTATCTGAA[A/G]CTTGTCTGCAGCATT	154214
rs763496080	snp	C/T	1.65825e-05	0.00287941	intron-variant	RNF217	GRCh38.p7	6:125076645	TTCTCCTTCCCTCTC[C/T]TGCTGATACAGATCC	154214
rs763548371	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124971233	TAAACTTATATTTTT[A/C]TTTTTCTTTTAAGTT	154214
rs763567879	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125043001	AGAAACTATCTCTCA[C/T]ATTCTGAAAACTGCA	154214
rs763581953	in-del	-/A			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981863	CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAT	154214
rs763666580	in-del	-/AC			intron-variant	RNF217	GRCh38.p7	6:125060358	TATATATGTGTATAC[-/AC]ACACACACACACACA	154214
rs763678260	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124969315	ATAAAGAAAACACAA[A/T]TTTGCTCAGTTTGTT	154214
rs763704599	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125039838	TTGAACAACCTGCTC[C/T]TGAATGACTCCTGGG	154214
rs763708148	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050132	TTTACTCATACAGGT[C/T]TTACTGAGGTAGGTG	154214
rs763722884	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125068507	ATAGCTTATGAATAT[A/G]TATTTGTTAGTACAA	154214
rs763754389	in-del	-/TG			intron-variant	RNF217	GRCh38.p7	6:125013354	CATGTTTTGTGTATG[-/TG]TGTGTGTGTGTGTGT	154214
rs763794640	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125034815	TCACGATATTGATTC[-/T]TTCCTACCCATGAGC	154214
rs763816450	snp	A/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009443	CTTTCAGATGGTGCC[A/T]TCTCTTTCTAGAAAG	154214
rs763819592	snp	A/C	7.5358e-05	0.00613786	intron-variant	RNF217	GRCh38.p7	6:125081406	GTTAGTTTTAAGACT[A/C]CTTAAATAATTTTGC	154214
rs763883080	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125028055	GGAGTAGTTTGAAAA[C/T]ACTTTCTCCCATTCT	154214
rs763926654	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997108	TTTCTGTTTTGGTCC[A/G]GTGTGTATTCATTTG	154214
rs763943935	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124985458	AATAATCCAATTATA[C/G]TCTTAGTTATTTTGG	154214
rs764000955	snp	C/T	5.08324e-05	0.00504119	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045412	AAAAAAGGACATATT[C/T]CCACCCCTTCCAGAT	154214
rs764018189	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048889	TATTATGTTCTGAAC[A/G]TCGTCAAACTCATAC	154214
rs764065472	snp	A/G	1.64988e-05	0.00287213	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125076842	TTTAAGGAGATTAGT[A/G]CGAGGGTCAGTCTGT	154214
rs764099012	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125061474	ATTTTCTGTTCATAC[C/G]CTTTGCCCATTTATG	154214
rs764107622	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076352	AATTGCCTCCTAACC[A/G]TTGAATTAGGTGTAT	154214
rs764108290	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125027628	ACAGAAGTGTAGAGA[C/T]CTCTTCAATATACTG	154214
rs764136763	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988354	GCTCAAAATACTGCA[A/G]TAAAACTTTACGACT	154214
rs764171070	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125075684	CCATATCAGCAATGT[A/G]ACCAAAATATTATGT	154214
rs764178122	snp	C/G	7.78584e-05	0.00623884	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962771	GGAGCCTGGGGCCCC[C/G]GGGCTGGAGTAAGAG	154214
rs764178144	snp	A/G	1.65198e-05	0.00287395	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058035	TACAAAAAAGGAGAC[A/G]AATTGTTGCGTCACT	154214
rs764224639	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124974584	ATTCTGTATAGCATA[A/G]TTTCCTTTCCATTAG	154214
rs764244722	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089255	TTCAGAAATTGCTTC[A/G]TGACTGTTGTAAGAT	154214
rs764265554	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125007200	TCATTTTTTCATGCA[A/G]CCTTCTTCTTGCCTA	154214
rs764265806	snp	C/G	0.000108629	0.00736903	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962860	TTGCCACTGCAGTTG[C/G]AGCTGGAGGAGGAAG	154214
rs764274545	snp	C/G/T			intron-variant	RNF217	GRCh38.p7	6:125032052	AAACCCATCAGATCT[C/G/T]GTGAGACTTATTCAT	154214
rs764291553	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124973013	ATATATACTCTATAA[A/G]TAGAGTGGATGTTTA	154214
rs764315354	in-del	-/TG			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085038	ATGTCATATGTATGA[-/TG]TATATATGAAATATT	154214
rs764354039	snp	C/T	3.95671e-05	0.0044477	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962947	GGCGAAGAGCTGGAG[C/T]CCAGGACCCGCGTGG	154214
rs764381746	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125056778	TTATTAATCCATTGT[A/G]ATCACATGGGGCTCT	154214
rs764403370	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087332	TTAATTTTATAAGCA[A/G]CCTGCACATAAGCCT	154214
rs764431103	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124965288	AATAATAATACACAT[C/T]ATTGGCCGGGTGCGG	154214
rs764436189	in-del	-/GGACACCAGCGCCCCAGAGCCCGCGA	0.000127992	0.00799872	frameshift-variant, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962729	CGACTGGGGCTGCGC[-/GGACACCAGCGCCCCAGAGCCCGCGA]GGACACCAGCGCCCC	154214
rs764441747	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011957	GGAGTCCCCACCAGG[A/G]GGGGCTGGCCAGATG	154214
rs764452417	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021947	AGTGCACTGGCATGA[C/T]CTCAGCTCACTGCAA	154214
rs764527585	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125012815	TCTGTGTTCATCTTT[C/G]AATTTCTTATTTATA	154214
rs764554068	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125061768	TTTTATATATTTACA[-/T]TATCTTTGTATATCT	154214
rs764569999	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019793	GGCCTCCTGGATTCC[A/G]TGTTGCCTGCTCTCT	154214
rs764572211	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091032	ATGAAATGTTGAGAA[A/G]TAAGGAGTATCTTAA	154214
rs764577352	in-del	-/CTCC			intron-variant	RNF217	GRCh38.p7	6:124976251	TTCTTCCCTCCCTCA[-/CTCC]CTCCCTCCCTCCCTC	154214
rs764627119	snp	G/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968184	TTCACACAGGTGAAT[G/T]TATAGAACCTGTCAT	154214
rs764631077	in-del	-/AG			intron-variant	RNF217	GRCh38.p7	6:124979046	AAGAAACCAATAGAG[-/AG]AGAGAGAGTGTAAGA	154214
rs764634677	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125017106	TAGCTGTGAGTACAA[C/T]TTAAAATTTTTAAAA	154214
rs764656812	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044824	AAACACCTTTTATTT[A/G]GCATGTTGTCTAAAT	154214
rs764703037	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124984065	CCAAAAGCCCCACTT[C/G]TTAATACCATTCACC	154214
rs764746678	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125031136	GCTGGAGCAGCTGGG[A/T]CACAGGGCACCAAGT	154214
rs764754932	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125045928	CTATAGAGCAAATGT[C/G]ATACAGTCCCTGCTT	154214
rs764817509	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125061178	TACCTTTGAAAGCAT[A/G]TATTTATAAAGGTAG	154214
rs764838173	snp	A/G/T	3.29784e-05	0.00406058	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009317	AAGCCACATTTATTT[A/G/T]TGCTGCAGGAGCCCT	154214
rs764846392	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995642	AAAAACATTTGGAGG[A/G]CGGGTGCTGTGGCTC	154214
rs764928536	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125002264	TGAGGAATTTAGCTG[C/G]CACTTTCCAGGCACC	154214
rs764936292	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124966315	AATTTCCTCATCAAT[C/G]AAATGTAATTGCAGA	154214
rs764954459	in-del	-/TTTG			intron-variant	RNF217	GRCh38.p7	6:125063478	CTTTGTCCGGTGCTC[-/TTTG]TTTGTGGTGTTATCA	154214
rs764957594	snp	A/G	1.76033e-05	0.00296671	intron-variant	RNF217	GRCh38.p7	6:125057909	ACTTTCAGTATATCC[A/G]CTAGTAATTAATATG	154214
rs765016868	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003496	ATCATTATCATCATC[A/G]TCATCCAAAGATGAT	154214
rs765044428	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042414	TAAATTGCTAGAGCT[A/G]GTAGTGGGTAGGTAT	154214
rs765062857	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124981144	TTTATAATGTTTGTG[-/A]AAAAAATTGATAAAA	154214
rs765067697	snp	A/C/T	7.47168e-05	0.00611178	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082942	TGCACTGGTAACATG[A/C/T]AGATGATTTCATCCA	154214
rs765094981	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995789	TAGCTGGGCGTGGTG[A/G]TGGACTTCTGTAATC	154214
rs765137740	snp	A/G	3.3769e-05	0.00410893	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081515	TGTAATCGGTAAGAA[A/G]CACTTCATGCATCTG	154214
rs765138007	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125027957	ATTCAAATCATTGCC[C/T]ATTTTTTAATCAGAT	154214
rs765162682	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124987914	GATTGGATTAATTAA[C/T]ATACATTAGAAAGTC	154214
rs765166165	snp	G/T	0.00130245	0.0254858	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125046614	CATTACAGCAAAATG[G/T]CAGGATGAAGTGGTT	154214
rs765186926	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982353	ATCATGACAGTTTAG[C/T]ATTTTTCCTCAAAAG	154214
rs765208922	in-del	-/GCG	0.00056185	0.0167514	cds-indel, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962570	AGCAGAGCACGGTGA[-/GCG]GCGGCGGCGGGCCCC	154214
rs765221902	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012722	TATTTTACTTTTGTA[A/G]TGTGCAAGTGTCACT	154214
rs765226965	snp	C/T	5.9363e-05	0.00544775	synonymous-codon, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962742	CGCGGACACCAGCGC[C/T]CCAGAGCCCGCGAGG	154214
rs765227404	snp	C/T	1.77055e-05	0.00297531	intron-variant	RNF217	GRCh38.p7	6:125081423	TTAAATAATTTTGCC[C/T]TTTGTTTTCCAGCTG	154214
rs765244414	snp	C/T	2.13077e-05	0.00326395	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962970	CCGCGTGGGGGCCGC[C/T]GACGGACTGGTCCTG	154214
rs765245379	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125071334	CAGCTGGCAGTCACC[C/T]GTGCCATCACGAGGG	154214
rs765252141	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B, missense, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964867	AAGTCACTGTGAGAG[C/T]AGATGTGTACAAAAG	154214
rs765264843	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089075	GTGAGCATAATTTAC[C/G]TTGGCTTATTTTATT	154214
rs765302448	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087385	TTATATTTTTATTCT[C/G]CCATATTTGTGGCTG	154214
rs765313944	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998904	TCACTTTGGTCCAGA[A/G]CAATGCCTTACATGT	154214
rs765334754	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998393	CTTTTCCTAAAGCCT[C/T]ATGTAAATCTGTCTG	154214
rs765491122	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125082581	GAGTATCATAGTGTG[C/T]AAATGATATGACTGT	154214
rs765500906	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124991607	TGGTTTTGTTGATTC[A/G]TGAGGCCTGAGTGCT	154214
rs765576474	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124978339	TGCATTCCGCTTGTG[A/C]CCCAGACCAGATCCT	154214
rs765577082	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084722	TATTTCCAGTTAGAG[A/G]AGTGTGTGACATTTA	154214
rs765581679	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125038486	ACATGGGAGGGCCAT[A/G]TTATTCAGGGTATAG	154214
rs765585204	snp	A/G			intron-variant, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124971581	CTGCCTCAGCCTTCC[A/G]AGTAGTTGGGACTAC	154214
rs765603042	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125010742	CTACTACCCTATTAC[C/G]CACAGGTTAAACCAA	154214
rs765713186	snp	C/T	1.6563e-05	0.00287771	intron-variant, synonymous-codon	RNF217	GRCh38.p7	6:125082544	TTGTTAAGTGATATG[C/T]TATACTGCCTGAAAC	154214
rs765734852	snp	A/G			intron-variant, upstream-variant-2KB, synonymous-codon	RNF217, RNF217-AS1	GRCh38.p7	6:124963711	TATACAGGATTGCAA[A/G]CACAAGCTTGCTCAA	154214
rs765735777	in-del	-/ATG			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087178	CTTCTCCCTTGTTAA[-/ATG]ATGAAATTGTTTTTA	154214
rs765777088	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979605	GGAGGCAATGAGGTT[A/G]CAGCAGCACAGAGAG	154214
rs765787777	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124981177	TAAAGTAATTAAAAA[A/T]TTTGATTTTATATTT	154214
rs765801732	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011767	TCCCATCTAGTTCTT[C/T]ACTTTTCATTGCATT	154214
rs765813089	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054805	TTTTGGCTCTGAGGT[C/T]TAAGGATTCATGAAT	154214
rs765846250	snp	C/T	1.68704e-05	0.00290429	intron-variant, synonymous-codon	RNF217	GRCh38.p7	6:125082483	CTGGAACCTCATAAG[C/T]GGTAGAACCAGGAAT	154214
rs765904479	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125056496	AGTACTTTTACTTCA[C/T]AGTTGCACAAGAGGA	154214
rs765921111	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083902	TACATTTTGGAAAAC[A/T]TGCTTCACTCTATAG	154214
rs765997257	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990777	GTGATCTCAAGAGTG[A/G]AGCCAAATTGGGCAT	154214
rs766032831	snp	C/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961730	CTCTGAACTCGACAT[C/T]CTAAATAGCCAGCGT	154214
rs766036814	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075413	CATGGTTCCGCATGC[C/T]TGGGGAGGCCTCAGG	154214
rs766042548	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125064483	ACCTATAATATTTTA[-/T]TTTAAAAATCAATAT	154214
rs766071429	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125014552	CCATCTCTGTGATGA[A/T]TGCATCATCTCACTG	154214
rs766084371	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125000368	TGTATATTAGGTTAC[A/T]CTTTGAGAAACACAC	154214
rs766087375	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124993331	AGAGTGCCTAGAACA[A/C]TAACTGGCAGATAGT	154214
rs766093874	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125070011	CCTTTCCCACTCTTA[-/C]CTCCTATTCCTAGTC	154214
rs766094463	snp	C/G	1.81273e-05	0.00301053	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962841	GCCTCTCAATCCCCA[C/G]ACCTTGCCACTGCAG	154214
rs766144495	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005733	TTCATGTGGTTATTT[A/G]TTCTGTTATTAGATA	154214
rs766198327	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125003820	ATAAGAAGCTCATAG[C/G]TTCTTATATGCTATG	154214
rs766203508	snp	A/C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091344	TATTTTTTTCACTTG[A/C/T]CTTTATTTCTTATCT	154214
rs766252266	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124972704	CTTTCTTTCCTTGCT[G/T]CCCTAACTCTCTTTG	154214
rs766278376	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041420	CATAAAACCAGTGAT[C/T]TGTATTGTCTTTATA	154214
rs766363311	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067592	GATACCATAAACTAA[A/G]ATAAAATAATGGAGA	154214
rs766371835	snp	A/C	3.29957e-05	0.00406162	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009330	TTGTGCTGCAGGAGC[A/C]CTTGTAATCTCTTCA	154214
rs766380378	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054716	CTGGGCGATGCAGTC[A/G]CATGGTATAGAGCAG	154214
rs766383864	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980771	ACTGAGTTGCCCCTC[C/T]CTCCATACTTTGATT	154214
rs766392753	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124983765	GTAATAACTATAAGA[A/C]TCTTGGAAAAGATAC	154214
rs766400405	snp	A/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960695	CATTATTGTTACTCT[A/G]GTCTTAGCCTGTTGT	154214
rs766410940	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125069959	TGCACCCATTATCCG[A/C]GCAGTGTACACTGTA	154214
rs766464650	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125026046	ATAGCCCATATGATC[A/G]TGGAGACCATCTGCT	154214
rs766482798	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086335	ATAAAAATAAAATTT[A/G]AGGAGATGTGTGTCA	154214
rs766488622	snp	C/G			intron-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963497	TCCTGCTCTCGATCT[C/G]ATCTCCCTGCTCGCG	154214
rs766493360	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125072705	TTTGAAGGAAGAATG[A/G]CACAGAATGGCAAAA	154214
rs766544818	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125042532	GAAAGAAGGGAAGGT[-/A]AAAAAATAGTCAATG	154214
rs766553513	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125010560	AAATCTCCAGGAAGT[C/T]TTGTTTAAATGTGCT	154214
rs766569073	snp	A/G			downstream-variant-500B	RNF217	GRCh38.p7	6:125092888	CATGAGGCATGAAAA[A/G]GAAGCAAATAGTGTG	154214
rs766581518	in-del	-/GGCATCTGGTGAA			intron-variant	RNF217	GRCh38.p7	6:125004980	CAAGTGTATGGTGCT[-/GGCATCTGGTGAA]GACTTTTGTGCTGTG	154214
rs766596434	snp	C/T	1.64928e-05	0.00287161	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076772	TTTTTGGAGACCACA[C/T]ATCAAACCTCAGTAT	154214
rs766626281	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002121	AATACTGGAGAGACT[A/G]ATAATCTCCAGAATG	154214
rs766633852	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030135	TGAGACTTATTCACT[A/G]TCACAAGAATAGCAT	154214
rs766641371	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124997251	CTCCATGTATTTGCA[C/T]GTATGGCTGCTTCAC	154214
rs766737934	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049065	TACCGTTCCATTTCT[A/G]CAAGGTTGACGTCAG	154214
rs766744819	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125022305	TATGTAAAATTTATA[G/T]AGCTCCATTATATAC	154214
rs766765475	snp	C/T	1.78854e-05	0.00299038	missense, synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125082882	TATTTGTATTTCCTA[C/T]CTATTGCCTTTGTAA	154214
rs766788131	snp	C/G	1.88308e-05	0.00306839	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082947	TGGTAACATGCAGAT[C/G]ATTTCATCCAGCTAA	154214
rs766790811	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125076990	GAGGATATTCTCTCA[C/T]CCTTTAAGAATAAAA	154214
rs766793772	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084303	GAAGGAAATATTTTC[A/G]GGAAGTTTTTCTCAA	154214
rs766811373	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125025349	GGACTGGAGACCAAG[C/G]CACACAATCCTAACG	154214
rs766819854	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125037433	ATTGATCACTTTTAC[C/T]TGATGTACTTAAATG	154214
rs766873606	snp	A/T	1.65381e-05	0.00287555	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076661	TGCTGATACAGATCC[A/T]CATCCAGCGAACTGA	154214
rs766875130	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125035595	TGTTCCAAATCTCTT[C/G]TCACACTTTTGTTTG	154214
rs766881101	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124976934	GGAAAGCTTAGAAGG[A/T]ATGCTAAGCAGGAAA	154214
rs766891570	in-del	-/TGTGT	6.62625e-05	0.00575559	intron-variant, frameshift-variant	RNF217	GRCh38.p7	6:125082525	TTTGGCTCCACAGCC[-/TGTGT]TGTTAAGTGATATGC	154214
rs766965003	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125037683	CTGCCCTGATGGTGC[A/C]CCTCAAAGTAATTAA	154214
rs766969692	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125079206	ATGATTAGCAGCCTC[C/T]GACATAGGGGCATCT	154214
rs766974235	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054145	GAGATTAGACATCTA[C/T]ATCCCTAATGGAAGT	154214
rs766983323	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124987592	TCAGAAAATGTGTCT[A/C]CTGCAAATTAGTGTG	154214
rs766998532	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972798	CCTATATCTAGATTA[A/G]GCATCCTTCCTATAT	154214
rs767031361	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006904	CAATGAGCCGAGATC[A/G]CGCCATTGCGCTCTA	154214
rs767042483	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125068645	ATATTTGTTTATACA[C/G]TTGGTTAATGTCTGT	154214
rs767057765	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125067079	TGTGGAGGATTGTTG[G/T]GTGGATTATGGCATG	154214
rs767143586	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125040001	TCAGAAAGCTGGAAA[G/T]ATCTGAAATCAACAC	154214
rs767196404	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124979912	GGTGGAGATGGCTCT[C/G]TCTCATGTCCTGTCA	154214
rs767220443	snp	A/C	1.65734e-05	0.00287862	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058075	AAATTGAGCATGGGC[A/C]GAGGAATGCCCAGAA	154214
rs767241878	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013057	AAAAGAATTGAAACA[C/T]ACTTGAAATAATTGA	154214
rs767251855	snp	C/G	3.33028e-05	0.00408048	intron-variant, missense	RNF217	GRCh38.p7	6:125082499	GGTAGAACCAGGAAT[C/G]AAACCCAACATTTGG	154214
rs767256229	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124988478	AAATGAATTTTATAA[G/T]TGACACTGTTGGTTC	154214
rs767284469	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124980995	TCTGTACGTTTGTTT[A/G]ATTACTGATTTCTCA	154214
rs767293904	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125018034	TTTATAAGTGTAACA[A/G]CTATCCATTTCTAAC	154214
rs767330312	snp	C/G	1.65375e-05	0.0028755	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045259	ATCACAGAGTGTTTT[C/G]AATTCTTGGAAGAAA	154214
rs767382006	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019339	CTATTACAAAAGATT[A/G]GAACTTACAACTCTG	154214
rs767400850	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124985721	TATAGTAAAAAAAAC[A/G]TAAATCAGATTTATG	154214
rs767460417	snp	A/G			missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076663	CTGATACAGATCCAC[A/G]TCCAGCGAACTGAAG	154214
rs767501612	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029525	TGCACAAAGATACTT[C/T]GTTTTGGCATGAAAA	154214
rs767518679	snp	C/T	3.35452e-05	0.0040953	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048221	CACAGTATGGCACCC[C/T]GTACTGAGACTAAGA	154214
rs767524093	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087576	GACAGTATACAAAGT[A/T]AAAGCAACTGATACA	154214
rs767551856	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124990255	ACTCTTATAAGTCTT[C/G]GTCCTTTTATCTTCT	154214
rs767552906	snp	A/G	1.67245e-05	0.00289171	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045402	AACCTTCAAGAAAAA[A/G]GGACATATTCCCACC	154214
rs767561535	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124976781	AAGTGCTGGGATTAC[A/C]GGTGTGAGCCAATGT	154214
rs767563174	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065429	AAATTACATGAGAAA[A/G]GCTCAATTCTGTATT	154214
rs767573746	in-del	-/A	1.68604e-05	0.00290343	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081513	GTTGTAATCGGTAAG[-/A]AACACTTCATGCATC	154214
rs767602407	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054033	TAATGTTAACTGATA[C/T]GTGATACCTAAACTG	154214
rs767614169	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124974911	GTTTCTTCCTGTTAG[A/G]GATCTGTATTCCCTG	154214
rs767624576	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084273	AGCTGCTTTTGGGAA[A/C]GGAAACAAAAAAGTG	154214
rs767631015	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125067303	GGTTTTATCCTCCAG[A/C]CTATAGGGGCCATTG	154214
rs767634617	in-del	-/G	0.000168591	0.00917972	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963238	TTCTACCTGGCGCCC[-/G]AGCCGTTCTCCATGC	154214
rs767635931	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125077902	CTTAGAAGCATATGA[C/T]ACCTGATCAGAACAA	154214
rs767656707	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053130	TTCTACTCATTGTTG[A/G]AGGCCACATTCTCTC	154214
rs767663833	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124995856	GAACCCAGGAGGTGG[A/C]GGTTGCAGTGAGCCG	154214
rs767698785	snp	A/G	0.000105237	0.00725311	intron-variant	RNF217	GRCh38.p7	6:125057919	TATCCACTAGTAATT[A/G]ATATGATTTTTTTCT	154214
rs767757783	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125014368	CAGCCTCGGTACAAT[A/T]CTGTGAGGTATATGT	154214
rs767761318	snp	A/G	1.90453e-05	0.00308582	intron-variant	RNF217	GRCh38.p7	6:125081402	GTAGGTTAGTTTTAA[A/G]ACTCCTTAAATAATT	154214
rs767782858	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042664	TGTTGGATGGTATCC[C/T]GATGTGGTTGATTAA	154214
rs767784167	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046124	AGACAGATAAACCTG[A/G]TGAGCATTTCAGAGC	154214
rs767789057	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125051397	TAAAATGGTCTGGAA[A/G]ATATTCTGAAAGAAG	154214
rs767790928	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980222	AGATGTCCATAATTA[C/T]TTCACTGATTGTCAG	154214
rs767793348	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022843	CTCCTTTGTCACCTA[C/T]GTCCCTGCTTGACCT	154214
rs767853299	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125043476	TTTACTGACATGTTC[C/G]TGCAAAGCTTCAGTA	154214
rs767874731	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125043959	CTTTTCTGGTATTCA[-/AT]ATGTCACCCCATGCA	154214
rs767877424	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058808	TGTCTATAGTATAGG[A/G]ATCTGTTGAAGTTTG	154214
rs767885669	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125009938	TGGTTCATGCTTGTC[A/G]TTTTCTGTTCCCTTT	154214
rs767893055	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124978448	CTAGATGAGGGGAAT[-/G]CGGTGGTGCCTGATA	154214
rs767949098	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124966707	ACTGAATATTTTTGT[A/G]AAAGGAGATGCACAG	154214
rs767985962	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125024719	GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	154214
rs768037374	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967573	TATAACTTGGAATGT[A/G]TACACCTGTCCAATG	154214
rs768044617	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988598	GTTCACTAGCTTTTT[A/G]AATTTGTCAAACTAA	154214
rs768062760	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125075923	ATATATGGTGTATGT[A/T]TATATACCATACCAC	154214
rs768093587	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124988076	CCGCCTCCTATCAGG[A/T]CAGCGAAGGCATCAG	154214
rs768106376	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125022397	TAAGTAACAATTAAT[-/G]TTCTTTCACCTGAGC	154214
rs768124071	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125020116	AGAACTTCAGACAGA[A/G]CTGTTCACGAGAATG	154214
rs768136946	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125031496	AGAAATTTTTTTCAT[C/T]AGATACTCTAAATCA	154214
rs768141975	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998234	TCATTTTGCCCCTCT[A/G]TTCTCCTATCCCATG	154214
rs768170873	in-del	-/TA			intron-variant	RNF217	GRCh38.p7	6:125078416	GTCCATTCTTTATTT[-/TA]AATAGAGAAGTCATT	154214
rs768196087	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124972461	TTGGCACTCTCCTTC[G/T]TAGCCTTTCAACACC	154214
rs768203049	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125019265	ATCGTAGCTATTTAT[G/T]TTGGTATTACCTTAA	154214
rs768213053	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026940	TTAATATTAATATAT[C/T]AATGTTTATTATATT	154214
rs768213974	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006841	GTAATCCCAACTACT[C/T]GGGAGGCTGAGGCAG	154214
rs768284480	snp	A/G	1.80716e-05	0.0030059	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962734	TGGGGCTGCGCGGAC[A/G]CCAGCGCCCCAGAGC	154214
rs768286168	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062477	AACATATCTAGAATT[A/G]ATTTATAGAATATTT	154214
rs768288149	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124973998	GCTATGGCTGTCTAC[C/T]GAGTGCCCCCACATG	154214
rs768376392	snp	C/G	1.85314e-05	0.0030439	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962808	ACCGGCGCAGCCTGC[C/G]GGACTGGCACTCACC	154214
rs768382638	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125064757	AATAAGTACGTGTGT[A/G]TATATTATTTTTATA	154214
rs768455115	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041827	CAGAAGTCCATCACA[C/T]TACCTAGCCCATAAA	154214
rs768489235	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124976510	CCTGACCTCAAGATC[A/C]ACCTGCCTCGGCCTC	154214
rs768496802	in-del	-/TTTG			intron-variant	RNF217	GRCh38.p7	6:125052283	TACCTTGTCATGCGT[-/TTTG]TGTGTGTGTGTGTGT	154214
rs768543528	in-del	-/C	3.3269e-05	0.00407841	intron-variant	RNF217	GRCh38.p7	6:125076638	TCTTTCCTTCTCCTT[-/C]CCTCTCTTGCTGATA	154214
rs768545459	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025109	GCTAGAGGTCAAGAA[A/G]GAAACAGAACTCAAC	154214
rs768547750	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011404	AACTGAAGGCTCAGC[A/G]AGGATAGACAATCAC	154214
rs768575547	snp	C/T			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006140	TTTTTGGAGGTGACT[C/T]TGTCAGTTAAAGTGT	154214
rs768579715	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967295	GACTTGGCCTTTACC[A/G]CATTTTCCTAGGAGG	154214
rs768613861	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088500	AGTGAGACTATTCTC[A/G]TTGCTTCTTTGGAGC	154214
rs768615780	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125045121	TCCTTTATTGCGGTC[A/G]TGAAATAAGTAATAC	154214
rs768650789	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998684	CGTGCACCTGTAGTC[C/T]CAGCTACTCAGGAGG	154214
rs768698680	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125054389	AGCTGCCCAGGCAGG[-/C]CTCATAGAGAATCAG	154214
rs768701955	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125075043	GAGCAAGTACCTACT[C/G]CAAGTGCAAGCTTGT	154214
rs768744956	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078091	CAATAGCATTCAATA[A/G]TCAAGACTGCTTTTA	154214
rs768772374	snp	C/T	9.55155e-05	0.00691004	intron-variant	RNF217	GRCh38.p7	6:125048304	AAAAATTCAGTTTCC[C/T]TAATAAAATAAGGTA	154214
rs768791599	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001571	TCCTAGCAGTATGGC[A/G]TTTTAGTGATAAAAT	154214
rs768794979	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124992349	ATATTAAAACATGTT[A/T]TCTATTCCCAAATGA	154214
rs768817643	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983197	ATTTTTATCTTATGA[A/G]TGGGCCCATAACATT	154214
rs768832403	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076617	CTTTTTAAAAACTCA[A/G]CTAACTCTTTCCTTC	154214
rs768832951	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124968771	TCCTTAACTCCTGAT[A/G]CAAAAGACATAAAAA	154214
rs768877365	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125002705	CTTTCTGATAGTGTC[C/T]GTGTGATTTTCGTGC	154214
rs768884012	in-del	-/CAA			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960982	TGGCATTTAGACATC[-/CAA]TTCATACCTTTGCTT	154214
rs768884246	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021511	ACCTCGTGATCTACC[C/T]ACCTCGGCCTCCCAA	154214
rs768884933	snp	A/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124960947	AATTTTCCATTCTTG[A/G]GTCAGACCGATAGAT	154214
rs768921199	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124980129	TCGAAGGGATTTTTT[G/T]TTTGTTTGTTTTTAA	154214
rs768926405	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125065928	ATAGACTTCTCCAAC[G/T]CAGTATGTTCTCTTC	154214
rs768936944	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124989928	AGGGCTCCATTTTTC[C/T]TTGCAGCTAGTGTTC	154214
rs768938424	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125082329	ATTTTCGTATGTCAA[C/T]TTGGGTTTAGCAAGT	154214
rs768940616	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032333	TCCTAATTCAATTTT[A/G]ATAGGTAGAACTCCA	154214
rs768942521	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125005402	TATGGCTTGCATAAC[A/G]TAAGGGTACAAGGTG	154214
rs768982600	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041912	TTATGCACCACCAAG[A/G]AAGTAAAAACACTGC	154214
rs769003077	snp	C/T	1.68431e-05	0.00290194	intron-variant	RNF217	GRCh38.p7	6:125045204	CATCTGCTCTTCCAT[C/T]ATGCAGGTACAACTT	154214
rs769028321	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125069799	TGCAGCCTCACCAGC[A/G]TCTGTTGTTTTTTGA	154214
rs769028440	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083546	GTATATGCGTAGGGG[C/T]GTGAATGTGTGTGTA	154214
rs769032860	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007735	TAATTATTTTCCACA[A/G]ACATCCCTTATACTT	154214
rs769052445	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964686	GGATTATTTAAAAGC[C/T]TCTGAGAGACTGTTG	154214
rs769063695	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125040910	ATTCCTTCATGTTAA[C/T]TCTCAATAAATTAGG	154214
rs769078573	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125027500	TGTCATTCTTTTTTA[A/T]GGCTGAATAGTACTC	154214
rs769180272	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092466	TTGCATGGAAGAATA[A/T]AAAGACACTCACTCG	154214
rs769183733	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125014152	GTTTTCCCTGGAGTT[G/T]GTCAGAATGGATGGT	154214
rs769199644	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124995432	TCCCTAAACACTGTT[G/T]CTTAGTTGTGCACAT	154214
rs769201786	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:124973337	CTTATATCACCACCT[-/G]AGTTAGTCCTGCTGT	154214
rs769211684	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124980979	TTAGAAGAACATAAA[C/G]TCTGTACGTTTGTTT	154214
rs769287877	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125044226	AGAAAGGGTTTGGTG[G/T]TGTTTGTCATTTGGA	154214
rs769359610	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124985266	GAATATATACTCCAA[C/G]ATTATTGGGAACAAA	154214
rs769363123	snp	A/G			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964353	AGTCACTGCTTATAT[A/G]CTTTCACAGTATCTT	154214
rs769428583	snp	A/G	5.48832e-05	0.00523819	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962908	CGAAAAGAGGGAGGG[A/G]ATGAACAGCAGGAGG	154214
rs769446992	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088189	TTTTTATAGCCACAA[C/T]TATTAATTTGATAAA	154214
rs769449703	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124986843	AAGTATCTTGAAATT[G/T]GTAATATAGATTTAC	154214
rs769455446	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125014392	TATATGTAGATGAGG[-/A]AACTGAATTACAGAG	154214
rs769488937	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083271	CGCCTCTTCTGAGAA[C/T]TGCTTGGACTGTCTT	154214
rs769494438	snp	C/G	3.35003e-05	0.00409256	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045211	TCTTCCATCATGCAG[C/G]TACAACTTGGCCAAG	154214
rs769503062	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124973819	CAGAACCTAGGAACA[-/T]TAAAAAAAAAGAACG	154214
rs769517866	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124977768	TGGTCATAAGACTGT[A/G]ACTGAGACAAGATGG	154214
rs769519121	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968680	ATAACATTACAAGTA[C/T]TGCTGACCTAAGGCA	154214
rs769536932	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074604	GTTTTATTTTAAAGT[A/G]AAGAAAAATTTTCAT	154214
rs769570543	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124999429	TTCCCACTTCTTTTA[C/G]AAAAAGAGCAAATAC	154214
rs769588602	in-del	-/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981502	CATAGGTAGATAAGA[-/G]ACAAAAGATTACATT	154214
rs769600251	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125063817	ATGACCAAAAAAGCA[A/C]GCAGAAAAAAAGTGA	154214
rs769602647	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019183	TTTCATGACACCTCC[A/G]CGAGGAGGTTGTACA	154214
rs769643088	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997044	TCTACAAACACGGAC[A/G]TGCTGGTAGAGTCTA	154214
rs769671849	snp	C/T	1.66167e-05	0.00288237	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058084	ATGGGCAGAGGAATG[C/T]CCAGAAGTGTCCAAA	154214
rs769677319	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054594	ATTTCCATTCAACAA[C/T]GAGCACCCATGCTAC	154214
rs769702753	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125038037	AGAGGTCTTCATCAC[A/C]TGAGTCATTAAATTA	154214
rs769712635	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124980371	AAATAGGAACTACCT[A/G]CCACCCTCCCCTTCC	154214
rs769742138	in-del	-/CACATG			intron-variant	RNF217	GRCh38.p7	6:125080591	GCCCTGAAGCTGTGT[-/CACATG]CCGTAAGGTTTAAAA	154214
rs769783150	in-del	-/TTC			intron-variant	RNF217	GRCh38.p7	6:125033195	CCTACAGATTCTGTG[-/TTC]TTTTTTTTTTTTTAT	154214
rs769790024	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125023796	TGAACCTGGAGGACA[C/T]TACGTTGAGTAGGAT	154214
rs769794458	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011099	GTACCAAGAATGTTA[A/G]GAAAAGAAATGGAGC	154214
rs769818815	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125043270	TTCTCTTTCCTCCAG[A/G]CCTTTGCCCAAGTTG	154214
rs769822188	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125074027	AGCTCATGTTCTTTC[C/G]AACCTCTCTGTAAGG	154214
rs769834854	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085500	AAAAAGTATTATTTA[C/T]ATGTCAGTGCCAACT	154214
rs769885762	in-del	-/A	5.62035e-05	0.00530081	intron-variant	RNF217	GRCh38.p7	6:125048280	CATTTTTTATTTTGC[-/A]GTATTTTTAAAAATT	154214
rs769901639	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966306	CTATGCCTTAATTTC[C/T]TCATCAATGAAATGT	154214
rs769908235	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125011968	CAGGAGGGGCTGGCC[A/C]GATGCATCTTTAAAA	154214
rs769918196	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125013605	TTTAGTAAAGACTTA[C/T]AGAGTTCGTATTCAG	154214
rs769948922	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124992168	AGCATCACACTTTGA[A/G]TAGCAAGGCTGTAGA	154214
rs769955985	snp	A/G			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124981578	TGGCTCAGTGAATCT[A/G]CCTTTTTACATAAAC	154214
rs769983683	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092114	CAACAGGTAGGTCCT[A/G]CTGGACAGGACCTGA	154214
rs769989840	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125028563	GTAGTTCCAAAAGAA[-/AT]ATGTTTCTAGAATAT	154214
rs769994996	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125013866	CAAAGGACATGTAAC[A/T]GCAGCAACAATAAAA	154214
rs770019153	snp	C/G/T	0.000125321	0.00791485	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963061	TGCGTGGAGAGCGAC[C/G/T]TGCCCGAGGCCCCCG	154214
rs770041913	snp	A/C			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967188	AGTGACCTGTGTATG[A/C]GTGTGTGAATATGGC	154214
rs770065102	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125053254	TCTTTTGGTTTATAT[C/G]TGTCAGACCCCAGTA	154214
rs770080007	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125002592	TTATCTACGACCACA[C/G]CCACCCCGTTTTCCT	154214
rs770080449	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124999820	TTGTACTTTTCACAT[A/G]CTTTATACTTACTTA	154214
rs770095195	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058413	AAAATATAGCGTAAA[A/G]GTGATATAAAAGTAT	154214
rs770105941	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124972157	CCCTGTTTCCATTCA[C/T]TGTACTCAGGTCAGA	154214
rs770112534	snp	C/G	0.000405673	0.0142363	intron-variant	RNF217	GRCh38.p7	6:125076622	TAAAAACTCAGCTAA[C/G]TCTTTCCTTCTCCTT	154214
rs770121165	snp	G/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962161	CCGGCAGCCGGGACC[G/T]GTGATGGCGCGGGAC	154214
rs770149250	snp	A/G	1.65457e-05	0.00287621	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045343	TTGGAACTTGGCCGT[A/G]TTGATTCCAGCACCA	154214
rs770149416	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125051628	CATTTTCAAAAACCT[A/C]AGATTTGAAATAATT	154214
rs770160928	in-del	-/TAAG			intron-variant	RNF217	GRCh38.p7	6:125038268	GCAGCAAAATATCTT[-/TAAG]TACATTAAGTAGATA	154214
rs770199011	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125050606	GGTGTACTTTAAAAC[A/G]TGCTTAACCTTCCTC	154214
rs770219364	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125081165	TCCTGGTAGAATACA[A/G]TAAGCCAGTTGCTTT	154214
rs770239198	snp	A/T	2.16866e-05	0.00329284	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045480	TGTGGGTTAGATGTC[A/T]CATGGCAGAAGCAGC	154214
rs770257459	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125002941	TGTAAATCAGAGCAA[-/C]CAGGATGCTATGGAG	154214
rs770294888	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125069161	CTTAACTTGAAACAT[C/G]AAATTTTCTGTAACA	154214
rs770326977	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125040739	CAAAAAGCTTATCCA[A/C]CACGATCAAGTCGGC	154214
rs770327044	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125025298	GAACATTAAATAATC[C/T]TTCATTTGGCTTGGC	154214
rs770345660	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054484	CTCCAGTGGTCTGCA[C/T]TGTAGTCATTTAGCT	154214
rs770363577	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125029673	TTGGTAAAAATGTAG[-/A]AACGTGCATTTTTTA	154214
rs770395038	snp	A/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961428	CCATGATTTCCACTA[A/G]TGATCCAGTTTATTA	154214
rs770395629	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125004748	GAACCACAGCTCGTG[C/T]GTAATTCTGGTGTGT	154214
rs770415143	in-del	-/A	1.65282e-05	0.00287469	frameshift-variant, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045289	ACAACTGTTGTCTAT[-/A]ACTTAACGCATGAAG	154214
rs770424766	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091316	ATAACATTCATATAC[A/G]TTATTAGTGCCTTAT	154214
rs770433635	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125043197	GATCTTTAAGTTCAG[A/G]TGCATGTGCATTTGG	154214
rs770454179	snp	A/C	1.66125e-05	0.00288201	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045386	AGTGCAAGCACTTTA[A/C]AACCTTCAAGAAAAA	154214
rs770472870	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042296	TGTAGGTCTTGAGTG[A/G]GCCATGAAACTGGAA	154214
rs770491102	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124983921	ATTCACTGTCTGGTG[A/G]GGGCCTGTTCCTCAT	154214
rs770498796	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124996727	GATTACAATGAGACT[A/G]TAAGTCACAACAATT	154214
rs770501211	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125079021	CACAACTTGCTCCCT[C/T]AGTCTTGGAATACAG	154214
rs770506268	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124979727	TGGTAAATCTTCGGA[C/G]AGTTTGCTTGAGCTG	154214
rs770524768	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124977244	TGAATTTCAGCCACA[A/G]CCTTTGCATACTTGA	154214
rs770550469	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125060965	TACTATTTTCACCTA[A/C]CATTGCAAACATTTC	154214
rs770586640	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997646	GCATTGAGCACATTC[A/G]TAGGTCCTTGGAAAC	154214
rs770588054	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085100	TACATATATACCAAC[A/G]GGCTGAATAACATAC	154214
rs770601547	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000934	ATGGATATTTCAAAA[A/G]TATGGAAGTATGATG	154214
rs770656052	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124995131	TTATTTATACCACCA[A/C]CTTCTTCATCCATAT	154214
rs770671109	snp	A/T	0.000186133	0.0096453	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125046625	AATGGCAGGATGAAG[A/T]GGTTTCAAAGGCTGT	154214
rs770675552	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125073424	CTTGTATCTAATTTG[A/T]CTTTGTAAGTTGGAT	154214
rs770721582	snp	A/C	3.6186e-05	0.00425343	intron-variant	RNF217	GRCh38.p7	6:125058144	AAGAAAAAACATGTA[A/C]ATCTGGATGTGACTG	154214
rs770758540	snp	A/G	1.67335e-05	0.00289248	intron-variant	RNF217	GRCh38.p7	6:125082607	ACTGTGGACAATAAA[A/G]AAGATTTAAACCAAA	154214
rs770791685	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124965755	TATATTCAAATGTCA[C/T]GCCCTGTGACTTTCA	154214
rs770813714	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:124968188	CACAGGTGAATTTAT[A/G]GAACCTGTCATGCCC	154214
rs770825051	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988158	GGTTGCACGCTCCTT[A/G]TGAGAATCTAATGCC	154214
rs770859308	snp	C/G/T	9.50388e-05	0.00689285	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962931	GCAGGAGGCGCCCCC[C/G/T]GGCGAAGAGCTGGAG	154214
rs770901708	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125024481	CCAGCACTTTGGGAG[C/G]CTGAGGCAGGCGGAT	154214
rs770907474	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125066599	AAACTTCCCTTGGTC[A/G]CCTTATCTAAAATTT	154214
rs770934784	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022601	CTGGCCTACATGTGG[C/T]CTCTGCCCTGGTAGT	154214
rs770951296	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125053611	TTCTTTAGTTTTAGA[C/T]ACTGTTTTTATTTTG	154214
rs770983293	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125039511	TAATGGGAGACTTTA[A/G]CACCACATTTTCAAT	154214
rs771005045	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124976519	AAGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC	154214
rs771014940	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125067926	GAGAAACTGGAAAAA[-/A]GATGTCACTGAAGCA	154214
rs771032557	in-del	-/TGTA			intron-variant	RNF217	GRCh38.p7	6:125052306	GTGTGTGTGTGTGTG[-/TGTA]TGTGTGTGTGTGTGG	154214
rs771049647	snp	A/G	0.000165769	0.00910258	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963283	GCTCCACCCTACTCT[A/G]GCCTGGGCGGTGTAG	154214
rs771060888	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124979463	AGAGAGATGAGAGCG[G/T]AATGGTGACAGCAAG	154214
rs771102814	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124993566	TCTTGGCAGTGCAAA[C/G]GTGAACCTGACATGT	154214
rs771117118	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125025203	GGTGATTGATAATTT[C/T]GTAGAGAATGACTGA	154214
rs771147274	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124969319	AGAAAACACAATTTT[G/T]CTCAGTTTGTTTTGG	154214
rs771152650	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B, missense, utr-variant-5-prime, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124964788	GTATCATCATCCTCA[A/G]AACAGATTTCGCTGC	154214
rs771152817	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980258	GTTTTTTCAAAAACG[C/T]TGAGCCACCCTCTGC	154214
rs771170195	in-del	-/ACTC			intron-variant	RNF217	GRCh38.p7	6:125071362	GGGTGAACAACTGAT[-/ACTC]ACAGTGGACTGGGTT	154214
rs771210972	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125059381	TCCATTAAAGAACAA[-/C]TAGAAAATGAGGCCT	154214
rs771233796	snp	C/T	4.94523e-05	0.00497229	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009248	TAGTTCTCTTCTCAT[C/T]CACACCCATAAACCA	154214
rs771239862	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125069258	TATAGCAAGAGACAC[C/G]AAATAATTTTGAAAT	154214
rs771335646	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125062130	GTGAGTTTTAAACGA[C/T]TATGCCTTTGTTAAA	154214
rs771364082	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124970577	GGATGTTGAGTAGGC[A/C]GTTGGCGTCTGGCAT	154214
rs771377311	snp	C/G	0.00149254	0.0272771	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962716	GGTGGCTGCGGAAGC[C/G]ACTGGGGCTGCGCGG	154214
rs771390784	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125003199	TAGAAGAGATTTAAC[A/G]TTTGATTTTCAACAT	154214
rs771435759	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052696	GAAGCCATTCATCAA[A/G]ACTCATTTTCTCCTC	154214
rs771465588	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125038370	TTTTGTAGATATATG[A/G]TATCATGGTTATGGT	154214
rs771484734	in-del	-/ATG			cds-indel, nc-transcript-variant	RNF217	GRCh38.p7	6:125086783	AAGTCAGGTTACAAC[-/ATG]ATATCTTTAATTGTA	154214
rs771488393	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125065843	GTCGGTAGGCAAATC[A/G]TAAAGTTTTGGGGAA	154214
rs771492641	snp	A/G	3.61291e-05	0.00425009	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048181	GACATGGATACCCCA[A/G]CCAACCAATCGTGAG	154214
rs771499832	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125018861	GTGGTGATATAGATG[C/G]ACCATACTGAAAGTA	154214
rs771547283	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125021624	TTGAATTCAGAGTAC[A/C]TGTAGAATAAATATA	154214
rs771600782	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083668	GAAAGATGATGGCTC[C/T]TTTGTGGACATAATT	154214
rs771644581	snp	G/T	1.80007e-05	0.003	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082927	GATCACGGACAGGTA[G/T]GCACTGGTAACATGC	154214
rs771654882	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125002386	AAGTTACTTTTAATT[A/C]CTGCCCTACTTCTGC	154214
rs771690420	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090619	CCTTAACAATAGAAA[A/G]TTAGAAGAAATTTCT	154214
rs771713791	snp	A/C	5.49949e-05	0.00524351	intron-variant	RNF217	GRCh38.p7	6:125048273	AGGTGAACATTTTTT[A/C]TTTTGCAGTATTTTT	154214
rs771716205	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125052383	TCCTCAGCCTTTAGG[A/G]AAGTTTCTCTTTCCC	154214
rs771740846	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124977083	CAAACTAAAAACTTG[A/G]AATCAGAATTTTCCA	154214
rs771762455	snp	C/T			synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045441	ATCAGAAAGCAAATA[C/T]AAAGTAAGCATTTTC	154214
rs771770172	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042590	ATATATTCTTCGGAA[A/G]TTGAATAGATTTGCA	154214
rs771784589	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125075150	TTATGAGATGGTTTT[C/T]GCAATTTTTTTTAGC	154214
rs771786497	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088672	ATGTAAAAGGCAATA[A/T]TTTTTTTTAAATACA	154214
rs771804107	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125053383	AAAATGAATTGATAC[A/T]TGTGCTTCATTATTG	154214
rs771805754	snp	C/G	0.000138112	0.00830885	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962728	AGCGACTGGGGCTGC[C/G]CGGACACCAGCGCCC	154214
rs771810857	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966203	TTAGTTGGTTAAAAA[C/T]ACAGGATTGTGGTTG	154214
rs771834606	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125019299	TTCCAAATATACTTA[C/T]GCTCCTACATTAGAG	154214
rs771857682	snp	A/C	2.9301e-05	0.00382749	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963025	TCCCTCGCCAAGAGA[A/C]AAGTCTTCTGCTCCG	154214
rs771882693	in-del	-/TTTG			intron-variant	RNF217	GRCh38.p7	6:125035850	GTGGGTTTTTTTGTT[-/TTTG]TTTGTTTGTTTGCAG	154214
rs771894215	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042149	AGGCCAAGAGATTGC[A/G]TAGGTGATGAGTAAC	154214
rs771902225	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124979567	TGGGGTGGGCATAGG[A/C]ATGGCATGTTTTGAG	154214
rs771909387	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057462	GCTAGGATTACAGGC[A/G]TAAGCCACCACACCC	154214
rs771947822	snp	C/T	0.000176382	0.00938936	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963132	TCCGCCAGTGTTGAA[C/T]CCTCCCAGCACCCGC	154214
rs771957554	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124998870	GGTTGTAAACATGTA[A/G]TGGGCAAGGAATCTA	154214
rs772044426	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125037201	CACACTAATGTAATT[C/T]CTATAGCTCTATGAT	154214
rs772047387	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999547	TGTACTTTAGGCTCA[C/T]AGACTGTAGTTCTGC	154214
rs772063577	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987243	TGTTTCACATATCGT[A/G]TAGTTCACATATTTA	154214
rs772075644	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032516	TGTCAAGTAAAGAAA[A/G]CTAGGTGAATATTAT	154214
rs772077472	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125048772	GGGTAAAAAGAATAT[-/A]AAGAATAAGCAGTAA	154214
rs772079217	snp	C/T	3.35627e-05	0.00409637	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081496	CACTAGGGGCCATAG[C/T]GGTTGTAATCGGTAA	154214
rs772108121	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125064877	TACTAGAAAATGTAG[C/T]GTACCTTAAAACCAT	154214
rs772123322	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078606	CTTGATAACTAACAC[A/G]CTCCTATGATAGTGG	154214
rs772139265	in-del	-/AA			intron-variant	RNF217	GRCh38.p7	6:125080532	TTGTGAGTCTACTGC[-/AA]AGTTTCTCTCTTTCT	154214
rs772192120	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049636	TGTAGTAAGAATTAA[A/G]TGAAATCACACATAT	154214
rs772195220	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991392	ATCAATTTCTCCTAG[C/T]GGCCTTCTTTTAGCA	154214
rs772280278	snp	C/T	3.42431e-05	0.00413768	intron-variant	RNF217	GRCh38.p7	6:125045192	TTTTTTTCCTTCCAT[C/T]TGCTCTTCCATCATG	154214
rs772287419	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125071183	GATGGTCTGACATGA[A/T]TTCGACTTTTCTTAC	154214
rs772316844	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125032698	ATGTCTACTTTATAC[A/T]TTTTGGTTTATGAAC	154214
rs772339080	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092449	TTAATTATGAAATCA[A/G]ATTGCATGGAAGAAT	154214
rs772342392	snp	G/T	1.6519e-05	0.00287388	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057998	CCACTCTCCTTGGCA[G/T]GAAGGTGTTAACTGC	154214
rs772355649	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124978056	GAGCACAAAATATTT[C/G]CTTAGCACCATGCTA	154214
rs772368661	snp	G/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124983149	ATTGTCTTCAGAAGG[G/T]TCATAAATGCTCAGA	154214
rs772437817	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125072016	ATGAACTTTCTGTAA[A/G]TATAATTTAAACCTA	154214
rs772452968	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125024320	AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC	154214
rs772474669	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125016910	ACGTTCTGCACATGT[A/G]TCACATAAAGCATAA	154214
rs772501235	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048974	CTTGCCTTTTGTCAA[A/G]TCCAGTCTCACTTTT	154214
rs772525371	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125060924	TAAAAAGTTTTAGTT[A/G]TGATGTTCAAATAAT	154214
rs772530793	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124983706	CTTACTGGCTCAGTA[A/G]GAAGAGGCTTGGAGT	154214
rs772550591	in-del	-/TTTG			intron-variant	RNF217	GRCh38.p7	6:125052286	TTGTCATGCGTTTTG[-/TTTG]TGTGTGTGTGTGTGT	154214
rs772554318	in-del	-/AATTA			intron-variant	RNF217	GRCh38.p7	6:124974338	TCTTTTCAATCATTT[-/AATTA]AATATTTCCAATTCA	154214
rs772559702	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125015675	TCCAGTATATTTTCT[A/C]TATTTTCTACATTTT	154214
rs772599444	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994564	AATCTGTTTTCTCCC[A/G]TACACAGCTGCTTTG	154214
rs772619241	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125061988	GTTTATGGGATGACT[A/T]TCCCCTCATCAATTG	154214
rs772717510	in-del	-/CA			intron-variant	RNF217	GRCh38.p7	6:125008511	GTCATCAGCACAGTC[-/CA]GGCCTTGGTTTCCAA	154214
rs772720385	in-del	-/A			intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125006559	TAATTAATTTCAATG[-/A]AAAGCATACTATTCT	154214
rs772744366	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125084943	CGTAAATTCATCTTT[C/T]CTGAACTTAGGCATT	154214
rs772761444	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125024929	TGGAGTTGAAACCAT[C/G]GGAGTGGAAGAGTAA	154214
rs772776957	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124996568	AATCTGAATTCTGTC[C/T]CCACAGCTCTGTTGA	154214
rs772795055	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125015933	AAAAATTAAATTTTT[G/T]TTCACCAGCATAAGT	154214
rs772813959	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030961	CCTGGGCATCCGGGC[A/G]TTTCCCTACATCTTC	154214
rs772814741	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125053466	CAGCTCTTATATTTG[A/C]AGTGCTACTTTACAC	154214
rs772848444	snp	A/C	4.99654e-05	0.00499802	synonymous-codon, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045222	GCAGGTACAACTTGG[A/C]CAAGTAGAAATCAAA	154214
rs772882893	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125019312	TATGCTCCTACATTA[C/G]AGATTGACTTCCTAT	154214
rs772883898	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041111	ATGAGCAGTGAAGCA[A/G]TGCATTTATTAATTA	154214
rs772920306	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071163	GCAGATGGTTCCCAA[A/G]TTAGGATGGTCTGAC	154214
rs772923802	snp	C/T	1.65261e-05	0.0028745	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057988	GTTTTAAGTGCCACT[C/T]TCCTTGGCATGAAGG	154214
rs772933804	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124992748	TCTTTGTTGTAATGA[-/T]TTTTTTTTGTCAAAT	154214
rs772991085	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032678	CAGTTGTAAGAGATA[A/G]TTGTATGTCTACTTT	154214
rs773014054	snp	A/G	1.75816e-05	0.00296488	intron-variant	RNF217	GRCh38.p7	6:125057912	TTCAGTATATCCACT[A/G]GTAATTAATATGATT	154214
rs773069104	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124974201	CATTGACCTCAACTT[A/C]TTTTGGGCAAGTGTC	154214
rs773072195	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125081014	AAGCCCTCTGTAGGA[-/C]CTACCAGCTCTCCAT	154214
rs773079880	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125031671	TGGACCTTCTTGTTC[A/C]TATCACTATAAGCAT	154214
rs773102568	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125020584	TTTTTTTAAATTGCC[A/C]TGCTTTCTGATGTTA	154214
rs773106136	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125063567	AGTTACTATAAATAT[A/G]TTGTCTCATCCAAAC	154214
rs773131828	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124987560	TGCTGTTGGAATGTT[G/T]AAATCATAAATTGAG	154214
rs773171101	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092496	GGATGAAAACTATAA[C/T]GGTTTTCAAACTATT	154214
rs773188436	snp	A/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125006914	AGATCGCGCCATTGC[A/G]CTCTAGCCTGGGTGA	154214
rs773198003	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124994838	CTGAATTTTATAGCT[C/T]CGTGGCTGACTGTTG	154214
rs773209420	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125078773	GTCAAAGTAGGGAGC[A/G]GCTGGCTTTAAGATA	154214
rs773216477	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965403	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	154214
rs773225937	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057486	CACACCCAGACTGCT[A/G]CTGTGTTTTTTATTT	154214
rs773260524	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125069740	CCACAGTGATTGAAC[A/T]AATCCACATTCCCAG	154214
rs773272533	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124991408	GGCCTTCTTTTAGCA[A/C]CCCATGTATACATGC	154214
rs773272629	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125037328	AGTAGCTTTTAAACA[A/G]CAAACTACCAGCAAG	154214
rs773298345	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054706	AAATTGTGGCCTGGG[C/T]GATGCAGTCACATGG	154214
rs773312285	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125059092	CATAATAATAATAAA[G/T]GTACAGATTTACTAT	154214
rs773360316	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022858	TGTCCCTGCTTGACC[C/T]TGAGTTTTCTGTAGC	154214
rs773362867	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125014821	TTAATGTCAAGATAT[C/G]TCTTTTGTACTTTAG	154214
rs773430149	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124983609	GGTGTGGGGGAGATA[C/T]CTAACGATGTTTTCA	154214
rs773431379	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124983759	TGCCCTGTAATAACT[A/G]TAAGACTCTTGGAAA	154214
rs773448765	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979385	AGCAAGCATGTGGAA[A/G]TAGGGTGTGCAAGTG	154214
rs773504156	snp	A/C			downstream-variant-500B	RNF217	GRCh38.p7	6:125092770	GGAGCAGGAATGAAC[A/C]GAAATTCAAGGGTGT	154214
rs773551724	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125001881	GGAGAACAAATGTTA[C/G]TCCCATCAATTATTC	154214
rs773609949	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125060960	ATCATTACTATTTTC[A/T]CCTAACATTGCAAAC	154214
rs773626753	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125011461	GGGTTTTAGACCCAG[C/G]ATGCTCCAATTCCAG	154214
rs773699887	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125049030	CTCCCTAAAACTCTT[C/G]TCATGATGCCAGAAA	154214
rs773710803	snp	C/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967790	AACATAAATTTTTTT[C/T]TTTCTTTGAGAGAAT	154214
rs773748223	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125005066	GGAAAGGGGGCAGAA[C/T]TCCCAGGATAACAGC	154214
rs773786231	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124969004	TATAGCCTTGTTGGC[A/G]GTATTTTCCCCAGCT	154214
rs773814013	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125002934	TATATCATGTAAATC[A/C]GAGCAACCAGGATGC	154214
rs773866642	snp	A/G	3.63908e-05	0.00426545	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048167	GTAAGGAGAGCACTG[A/G]CATGGATACCCCAGC	154214
rs773945807	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125063426	AAATGTGCATAGTCA[C/T]TTCTGGATTCTGATA	154214
rs773985692	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125037311	CAAAATACCAGAAAC[G/T]GAGTAGCTTTTAAAC	154214
rs774025911	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125074207	GTGCCCGCCTGTAAT[A/T]TGCTGTGTTCCACTT	154214
rs774041466	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125050666	CATATATAAGAATGT[C/G]TAAAGCTTTCCCATG	154214
rs774079796	snp	A/G	3.72544e-05	0.00431576	intron-variant	RNF217	GRCh38.p7	6:125058153	CATGTACATCTGGAT[A/G]TGACTGAACAATATT	154214
rs774111651	snp	C/T	1.78481e-05	0.00298726	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082921	GAAAACGATCACGGA[C/T]AGGTATGCACTGGTA	154214
rs774159046	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125075049	GTACCTACTCCAAGT[A/G]CAAGCTTGTCCAACC	154214
rs774159220	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125044497	TGTATCCTCCCTTCT[C/G]TCCTAATCTAGCTTC	154214
rs774166768	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964597	ACTGAAAGTGTGTAC[A/G]GTCCCTAACTAAAAA	154214
rs774194892	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124994341	TCCTGACGTGATTTC[A/G]TCTGCAAGTCTTTCA	154214
rs774255998	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125073868	CATATGTGCCAAAAC[A/G]AGTTTGGCACTGTGC	154214
rs774291066	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124997993	CTCCGGCATTCCTTT[G/T]CTGATTGTGAGCAAG	154214
rs774299109	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076386	TGGAAAGATAAATGT[A/G]TCTTCCTTGGAATGT	154214
rs774331466	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125018971	TGGACATACACCTCC[A/G]GGCATAAAACTTGAG	154214
rs774335146	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031534	CAAGTTCAAAGTTTC[A/G]GTTCCACAAATCTCT	154214
rs774354946	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057429	TCAAGTGATCTAGCC[A/G]CCTCAGCCTCCCAAA	154214
rs774387625	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990107	ATTTATCACTCTATC[C/T]TCCTTGAAATACTTT	154214
rs774392794	snp	A/G	3.35048e-05	0.00409283	intron-variant	RNF217	GRCh38.p7	6:125082611	TGGACAATAAAGAAG[A/G]TTTAAACCAAAGTTT	154214
rs774399881	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090032	AACCCTTCTAAGACC[C/G]ATTTTTTTAAGTGTC	154214
rs774403072	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125016969	AATAAGGAAGTGTAT[-/A]AAAAAATAATGGTGT	154214
rs774414129	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124990214	TAATTAATCTCCTTC[G/T]GAATTACTTCTTAAC	154214
rs774497994	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125030947	GCAGCACACTTTTGC[C/G]TGGGCATCCGGGCGT	154214
rs774507439	in-del	-/TG	1.6522e-05	0.00287414	intron-variant	RNF217	GRCh38.p7	6:125076868	TCTGTGGTGAGTGTC[-/TG]ACATACTTATGGGTG	154214
rs774515801	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040956	TCTCAAAATAATAAG[A/G]GCTGTTTATGACAAA	154214
rs774519939	snp	G/T	0.000165851	0.00910484	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963287	CACCCTACTCTGGCC[G/T]GGGCGGTGTAGGGGA	154214
rs774525277	in-del	-/GTGG/GTGTGTGC			intron-variant	RNF217	GRCh38.p7	6:125052309	TGTGTGTGTGTGTGT[-/GTGG/GTGTGTGC]GTGTGTGTGTGGTTT	154214
rs774563918	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088015	TAAGTTACAAAATTC[-/T]TTTTTTTTTTTTTTT	154214
rs774572842	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124995576	TTTTTCATTGTTGTT[C/T]TGGAGTTTGTTGTAT	154214
rs774608016	snp	C/T	1.64838e-05	0.00287083	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009254	TCTTCTCATCCACAC[C/T]CATAAACCAGTTCAA	154214
rs774655684	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125069909	GTTTTTGGTTACATG[G/T]GTAAATTCTTTAGTG	154214
rs774696004	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125037106	GTCCTGCCCACTGCC[C/T]TGTAGTGTTCATATG	154214
rs774696162	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125021948	GTGCACTGGCATGAT[A/C]TCAGCTCACTGCAAC	154214
rs774713866	snp	G/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982986	GAAAGGGAAAGAAAA[G/T]GGAAGAAGCACATAT	154214
rs774728866	in-del	-/GGAG			intron-variant	RNF217	GRCh38.p7	6:125025759	GAGGAAGGGAAGGAG[-/GGAG]GGAGGGAGGGAGGGA	154214
rs774743398	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071065	AAAAGGCCACATTCC[A/G]GTTCTTTTTTTTAGA	154214
rs774785765	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022750	TACAATTACACATTA[C/T]ACGCTAGACAAAACA	154214
rs774797782	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030001	ACTTAAGAGTTACAC[A/G]TGGCTGGGGAGGCCT	154214
rs774810812	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125014199	TGATCCTGGAATAGA[C/T]TGAAAGCTCTTGCAT	154214
rs774837225	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067021	ACGAGGGTTCATGGC[A/G]AAAGGACTCAACACC	154214
rs774843263	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124980983	AAGAACATAAACTCT[A/G]TACGTTTGTTTAATT	154214
rs774885518	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125017581	ATAATCTTATTATGA[C/G]AAGTGTTCACATTTC	154214
rs774917630	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125058737	AGCAAACAGCCAGGG[A/T]AGACTCTCCTACGGG	154214
rs774991970	snp	C/T	0.000127992	0.00799872	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962729	GCGACTGGGGCTGCG[C/T]GGACACCAGCGCCCC	154214
rs775033400	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092481	TAAAGACACTCACTC[A/G]GATGAAAACTATAAC	154214
rs775056028	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124970775	CTGGGACATCAGAAA[A/G]AAGAAGCAAAGAGTC	154214
rs775120490	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062435	TTACTTACAAGTATG[A/G]TTTTTATAGTACGAT	154214
rs775139337	snp	A/C	1.81033e-05	0.00300854	missense, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082930	CACGGACAGGTATGC[A/C]CTGGTAACATGCAGA	154214
rs775148060	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124972398	GCTCTCTCCAACTTA[A/C]TCTCCACACATATGC	154214
rs775161484	in-del	-/CT			intron-variant	RNF217	GRCh38.p7	6:125019539	AACCTAAATTTTCCC[-/CT]TTTTATTTTTTAGCT	154214
rs775178583	snp	A/T	7.79879e-05	0.00624403	intron-variant	RNF217	GRCh38.p7	6:125048293	GCAGTATTTTTAAAA[A/T]TTCAGTTTCCCTAAT	154214
rs775181454	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019208	TGTACACCATTTGAA[A/G]ATCCCTTCCTTTGAA	154214
rs775203704	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049938	TTTAGGGCATCAAAG[A/G]GATGTCCAGAAAACA	154214
rs775207547	snp	C/G	3.06932e-05	0.00391735	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963030	CGCCAAGAGACAAGT[C/G]TTCTGCTCCGTGTAC	154214
rs775215478	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125053887	AAGAGTTTGTGCGTT[A/G]ATCATAGTGCTTAGT	154214
rs775227589	snp	A/T	2.03188e-05	0.00318732	intron-variant	RNF217	GRCh38.p7	6:125082821	AATAGGAAAACCTAA[A/T]TGCCTCTCATCCTAA	154214
rs775234529	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125034213	AATTGGAGCCCATTT[C/G]TCAATTTTTTCTTTT	154214
rs775253440	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011173	TCTTTTAAAGTTTTG[C/T]CTAAGGCTGACTCCA	154214
rs775275159	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125063197	AGATTAGATACTAAA[A/G]TCTGAGTTAAGAAGA	154214
rs775298910	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086870	CTGTGACTCTGACTA[C/T]CTCTTGAGTCCCAAG	154214
rs775303950	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054599	CATTCAACAATGAGC[A/G]CCCATGCTACACAAA	154214
rs775342251	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004887	CCATTTTTTGCTGCT[A/G]TAACAGAATACCACA	154214
rs775369950	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009841	AGTTAACCTGACCCA[C/T]GTTATATTACACAAT	154214
rs775372600	snp	C/T	3.39778e-05	0.00412162	intron-variant	RNF217	GRCh38.p7	6:125045196	TTTCCTTCCATCTGC[C/T]CTTCCATCATGCAGG	154214
rs775391910	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125043282	CAGGCCTTTGCCCAA[G/T]TTGTCTCTTTCATCT	154214
rs775432135	in-del	-/GCGCGGACACCAGCGCCCCAGAGCCC/GCGCGGAGCCC	0.00225892	0.0335449	frameshift-variant, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962725	GAAGCGACTGGGGCT[lengthTooLong]GCGCGGACACCAGCG	154214
rs775445296	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984078	TTCTTAATACCATTC[A/G]CCTTTGGTGTTACAT	154214
rs775487059	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125076059	ACTGCAACAATAGAG[A/G]AAGGTGCTTAGTTGC	154214
rs775511821	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963038	GACAAGTCTTCTGCT[C/T]CGTGTACTGCGTGGA	154214
rs775519536	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967189	GTGACCTGTGTATGC[A/G]TGTGTGAATATGGCT	154214
rs775522081	in-del	-/AT	3.53451e-05	0.00420372	intron-variant	RNF217	GRCh38.p7	6:125058137	GAGGAAAAGAAAAAA[-/AT]CATGTACATCTGGAT	154214
rs775538147	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124999821	TGTACTTTTCACATA[A/C]TTTATACTTACTTAT	154214
rs775565534	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125013893	AAAAGCAGTTCTTAT[G/T]TATTAATTTATGAAA	154214
rs775575509	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125072146	CCCCTGGTAGTACGA[G/T]TTTAAAATTACAACT	154214
rs775584558	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125057825	TTTGAGTCTTATAGA[A/G]GGGGAGGTATTTTAA	154214
rs775609329	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089171	TGCCTAGCCCTCTGC[C/T]AAGAAGTAAGTCAAG	154214
rs775613516	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124988210	TTTCATCCCAAAACT[A/G]TCACCCCTGACCCCC	154214
rs775618048	snp	A/T	1.89813e-05	0.00308063	intron-variant	RNF217	GRCh38.p7	6:125081403	TAGGTTAGTTTTAAG[A/T]CTCCTTAAATAATTT	154214
rs775633708	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124966330	GAAATGTAATTGCAG[A/G]CAACCTGTAATAACC	154214
rs775647723	in-del	-/TAAC			intron-variant	RNF217	GRCh38.p7	6:125055955	AACAGTTATTTTAAA[-/TAAC]TAAAGAGTAACATCC	154214
rs775654298	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998922	ATGCCTTACATGTAA[C/T]AGGCCCTGAAAAAGT	154214
rs775658868	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125050619	ACGTGCTTAACCTTC[C/T]TCCTGGTAAAGATAA	154214
rs775679340	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125081363	TACACTGTGGTATTT[A/G]AAAAGCATCACTGTA	154214
rs775690239	snp	C/T	1.6517e-05	0.00287372	synonymous-codon, nc-transcript-variant	RNF217	GRCh38.p7	6:125058013	TGAAGGTGTTAACTG[C/T]AAGGAGTACAAAAAA	154214
rs775708648	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125028716	CTCTTTTTACACTTG[A/T]ACCTGTGTTTCACTT	154214
rs775761183	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124989605	GATGAGCATGGCTAT[A/G]TTCCAATAAAGCTTT	154214
rs775799985	snp	A/G/T			intron-variant	RNF217	GRCh38.p7	6:125067012	GAGTATTATACGAGG[A/G/T]TTCATGGCGAAAGGA	154214
rs775818319	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124979688	TAGATCCTCCATGGA[A/T]ATTATACTTTATTTC	154214
rs775825077	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081634	TATGCCTGCTTTAGA[C/T]AGATTACCAGCATAT	154214
rs775865238	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124979816	TTTAAGGGTTGAGTT[A/G]GCAAGAGTAGAAGCA	154214
rs775938621	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125042299	AGGTCTTGAGTGGGC[C/T]ATGAAACTGGAATGC	154214
rs775956154	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125025330	GCAAATGGACAGATG[A/T]TAAGGACTGGAGACC	154214
rs775960734	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125002782	CATTATTTTTGTAAC[-/T]TAAGTACTTACTGTG	154214
rs776002736	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993106	CAAATAGTAAAATAT[A/G]CTTGATATATGAACT	154214
rs776041678	snp	A/G	0.000291418	0.0120675	missense, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963361	GAAGACAAGCCCATC[A/G]AGCCCCTGCCTTGCT	154214
rs776047880	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125012735	TAATGTGCAAGTGTC[A/G]CTAATATTTGAATAA	154214
rs776061638	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125089380	ATAGGTATGGTTTAT[A/G]GTCTTTGTTTCAGCA	154214
rs776125718	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124996839	ATATTACTTATCTAT[C/T]TTTTACTATATAAAG	154214
rs776133537	snp	A/G	3.29669e-05	0.00405984	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009292	ATGAAGGTAAAGTAC[A/G]TAGATGAAGAAGCCA	154214
rs776224039	snp	C/T	0.000715905	0.0189061	synonymous-codon, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962736	GGGCTGCGCGGACAC[C/T]AGCGCCCCAGAGCCC	154214
rs776224636	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124983962	TTCTATGCATCCTCA[C/T]GTGACAGAAGGGGCA	154214
rs776228231	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125043201	TTTAAGTTCAGATGC[A/G]TGTGCATTTGGGTGC	154214
rs776242338	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125085443	ATTATTTGTGAATTT[C/T]TTACTAAGTTTCATC	154214
rs776254938	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125072114	TGGGGAATTCATCAG[C/G]ATAAGAAATGTATTA	154214
rs776255824	snp	G/T			missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081480	ATGGTTTTGGGATTG[G/T]CACTAGGGGCCATAG	154214
rs776272719	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125016714	CCACCTGTTCTCACT[C/G]ATAAGTGGGAGCTGA	154214
rs776303452	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027925	TGAGCATCTTTTCAT[A/G]TGCCTGTTCACCATT	154214
rs776311931	snp	C/T	1.83528e-05	0.0030292	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962816	AGCCTGCGGGACTGG[C/T]ACTCACCGGGCCTCT	154214
rs776346328	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:124973717	GTGGCCTGAGTCTTT[-/A]ATGCTAGCATCCCAT	154214
rs776346511	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125060971	TTTCACCTAACATTG[A/C]AAACATTTCTCATAT	154214
rs776366330	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125065011	TTAAAACTATGCAAT[C/G]ACGCCGGTAATCCCA	154214
rs776390420	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125016556	GCTGTTTTTAGAAAG[C/T]TTTTAGAAAGTTCTC	154214
rs776402090	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022649	ATCTTCTTATAAACC[A/G]GTGATCAAGGCCAAT	154214
rs776407828	snp	A/G/T	0.000117802	0.00767393	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081507	ATAGCGGTTGTAATC[A/G/T]GTAAGAAACACTTCA	154214
rs776454670	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125065901	GCTACTCAACATCTT[C/G]AACCGGATCTAATAG	154214
rs776493303	snp	C/T			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009713	GATATCAAAGCTTTG[C/T]TCTCCTAACTAGTAT	154214
rs776496034	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125017285	GAACAAAAACAGTTA[C/T]ACACCATATTGTATT	154214
rs776502315	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125032803	GAACATTCAGATAGT[A/G]AGGAGGGAAGAAAAG	154214
rs776509116	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092580	ACATGATGTGTGCAA[C/T]ACATCATGCAATGTT	154214
rs776535340	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125057750	GCCTACAAATAGCCA[A/C]GTCATCCTTGCCAAA	154214
rs776544504	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124968512	TGGCATTTGATTTCT[C/G]TAGAGGAATCCTCTG	154214
rs776585602	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125025205	TGATTGATAATTTTG[C/T]AGAGAATGACTGAAA	154214
rs776626509	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125011856	CAAAGAAACTCTTCT[C/T]GGTGAGATAATAACT	154214
rs776643846	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976587	TATTTATTTTTTTAG[A/G]TAGATTCTTCATAGT	154214
rs776647192	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124980281	CCCTCTGCTTCTCAA[C/T]AGTTTGCAATTTGCT	154214
rs776706582	snp	A/G	1.76474e-05	0.00297042	intron-variant	RNF217	GRCh38.p7	6:125057894	CTTATCCTTTTAGAC[A/G]CTTTCAGTATATCCA	154214
rs776724915	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125083930	TAGATAGATCCTTCA[C/T]ATTGGGATTATTTAA	154214
rs776741016	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125025444	CTGAAGTTAGCAGAG[A/G]GAGGTGAGATTCCTG	154214
rs776745482	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125036676	AAACATATTTACAAG[-/A]AAAAAAAACATCAAA	154214
rs776752400	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990734	AGTAAAATCTTAACT[A/G]TTCTCCCTGCCCTAG	154214
rs776775072	snp	A/C/G			intron-variant	RNF217	GRCh38.p7	6:125073840	GGGAAACAACTTTAT[A/C/G]TTGACCTGACTCCAT	154214
rs776804124	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125062232	TTTTATCTTATTTAT[A/G]TATTAAGCATTACTT	154214
rs776804706	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125068295	CTCAATTAGTAGATA[A/C]AATGCCATAAATATG	154214
rs776810385	snp	C/T	1.64879e-05	0.00287118	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009308	TAGATGAAGAAGCCA[C/T]ATTTATTTGTGCTGC	154214
rs776828490	snp	A/G	4.00032e-05	0.00447214	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962950	GAAGAGCTGGAGCCC[A/G]GGACCCGCGTGGGGG	154214
rs776857393	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124966234	TAATATTTTTGATCT[A/G]TGTCAATTCTATGGT	154214
rs776867488	in-del	-/TGGTGTGCAG			intron-variant	RNF217	GRCh38.p7	6:125007293	TCTTGTTGCCCAGGC[-/TGGTGTGCAG]TGGTGCGATCTCGGC	154214
rs776888142	snp	A/G	3.53014e-05	0.00420112	intron-variant, stop-gained	RNF217	GRCh38.p7	6:125082471	AATTAAGACTTACTG[A/G]AACCTCATAAGTGGT	154214
rs776891257	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125069280	TTTTGAAATCAGCAT[C/G]TATTTATTTTTGCAG	154214
rs776895244	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125056220	AGCCAGACAAACTTA[C/T]GTTTAAATTCCTTCT	154214
rs776926827	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125049075	TTTCTACAAGGTTGA[C/T]GTCAGCTTCCAACTA	154214
rs776968282	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124991528	TGTGTTTTATTTATT[A/G]TATTCATTTTTGTTG	154214
rs776983380	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057626	GCCTGAGTGTGTGGA[C/T]TTGGGGCCTTGTGAG	154214
rs776993024	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125028413	CCCATTTTTTATTAG[G/T]CTATTATATATTTCT	154214
rs777059419	snp	C/T	4.94849e-05	0.00497393	stop-gained, nc-transcript-variant	RNF217	GRCh38.p7	6:125076753	AGATACCGCCAGCTC[C/T]GATTTTTTGGAGACC	154214
rs777092264	snp	A/T	1.68216e-05	0.00290009	intron-variant	RNF217	GRCh38.p7	6:125045205	ATCTGCTCTTCCATC[A/T]TGCAGGTACAACTTG	154214
rs777159278	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125004744	ACAAGAACCACAGCT[C/T]GTGTGTAATTCTGGT	154214
rs777176681	snp	C/T	4.96931e-05	0.00498439	missense, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963004	GTGCTGGGTCAGCGG[C/T]GCCCGTCCCTCGCCA	154214
rs777183188	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125066375	GGACATGTCCCCACT[C/T]TGTGACTCCTCTAGT	154214
rs777210918	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125078479	TCCAAGATGTAGTGG[A/C]TGCATCTGGTGAGGG	154214
rs777223643	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125068679	CATGTATAAGCTCTT[C/T]AAAGGCAGGAGCCCT	154214
rs777268379	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125022469	CAGGCTGACAGGGCC[A/G]GAAAGGTTTTCCTTC	154214
rs777283605	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124972879	TATACAATTATTCTT[A/G]TTTCACTGTATTTAA	154214
rs777283853	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125067151	AAAGGCACAGAGCCA[A/G]GAAGTGTTTGATGTC	154214
rs777329065	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124976133	ACTGTTTGTCAAGTT[C/T]TCATGGTTATTTTTG	154214
rs777338428	in-del	-/AA	1.64836e-05	0.0028708	intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125009267	CCCATAAACCAGTTC[-/AA]AAGAAAGGGATGAAG	154214
rs777354034	snp	C/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125009573	TGGCAGCTGACTATT[C/G]TATTGCATTAGAATT	154214
rs777398183	snp	C/T			intron-variant, upstream-variant-2KB	RNF217	GRCh38.p7	6:124982660	GAGTCTATGCTAGAT[C/T]TTGCCTGAAAACAAA	154214
rs777409778	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125044304	TAATGCCATGAATAT[-/A]AAGAGTTATTGTTCA	154214
rs777410898	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124990789	GTGAAGCCAAATTGG[A/G]CATGGTGGCTTACGT	154214
rs777436147	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125044036	CAGATAAATAGCAAT[A/G]TTAAAAGTTACTATG	154214
rs777436214	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125015107	TCACTTAGAAGTTTC[A/T]TTGATACCAATGTGT	154214
rs777454978	snp	C/T	1.90776e-05	0.00308844	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124963090	CGCCTCGGAGCAGCT[C/T]TCGCCGCCCGCGTCG	154214
rs777512915	snp	A/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967093	AGAGCTCTAAATCCA[A/T]GGCAGAGATAGTTAT	154214
rs777548999	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054993	CATGTGGAAGAATAA[C/T]TGTAAATAAAAGAGT	154214
rs777587070	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997382	ATATTCCTGGAAATC[A/G]TTCCTACCCTAGGGC	154214
rs777596939	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125046908	TGTTAGAAAAAAATC[C/T]TATTTTTCTCTTCTA	154214
rs777597074	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125021362	ACCTGTACCTCCCGG[A/C]TTCAAGCAATTCTCT	154214
rs777601111	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968569	GGACTTTTTCCGAGG[C/T]ATGCTGCATGGGTAT	154214
rs777609753	in-del	-/TG			intron-variant	RNF217	GRCh38.p7	6:125001287	CTTGTTACCAGTTTT[-/TG]TGTGTTTGTTCTCCC	154214
rs777641608	snp	A/G	1.6528e-05	0.00287467	missense, nc-transcript-variant, intron-variant	RNF217	GRCh38.p7	6:125045280	TTGGAAGAAACAACT[A/G]TTGTCTATAACTTAA	154214
rs777645494	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125058403	CTTTATAGGAAAAAT[A/G]TAGCGTAAAAGTGAT	154214
rs777733605	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125059857	TTTAAAAGGGATTAC[C/G]TTTTAAATAGCTGAA	154214
rs777736692	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125048455	GTTTCTGTGCAATTT[A/G]ACGTCTCTTTATAAT	154214
rs777757267	snp	A/G	3.58282e-05	0.00423235	intron-variant	RNF217	GRCh38.p7	6:125058141	GAAAAGAAAAAACAT[A/G]TACATCTGGATGTGA	154214
rs777792787	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125080786	TGACATCCTTACCAG[C/T]ACTTTGCCTTTTTAT	154214
rs777810328	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125002433	AAATGCTGTCGTGCC[A/C]CCTGCACGCCCCTAT	154214
rs777822402	snp	A/G	1.97799e-05	0.00314476	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082966	TCATCCAGCTAAGCT[A/G]GTTGGAGTAGGAGCG	154214
rs777856327	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125050413	AAGCCAATAAAATTC[A/C]CTGGAGAAACTCTGT	154214
rs777865329	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125038204	CAGAAAAACTGAACA[A/G]CATCTTTTTCAGTGA	154214
rs777942750	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125051256	TGACCTGCACTGGTA[C/T]TAAGAACTGTTTTCC	154214
rs778005832	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125005997	GAACTTGGTAATGGG[C/G]TGTTAATTAATTAAA	154214
rs778013109	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124993547	TGGCACGCACTATTC[C/T]AGATCTTGGCAGTGC	154214
rs778022217	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125039363	AAAGAAGGGCATTAC[A/G]TAGTGGTAAAGGGAT	154214
rs778040180	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087590	TTAAAGCAACTGATA[C/T]ATATATTTCAGTGGA	154214
rs778044532	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125036146	GTGTTCTAATCGTTC[A/G]ACTCCCACTTATGAG	154214
rs778084754	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125049868	AGGAGCAGGTTTGGG[A/G]AATGGAAAATTAGTT	154214
rs778191148	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125018639	GTTTGTTAACTTAGA[C/T]GATTAAAAAAGGAAT	154214
rs778214875	snp	C/G			intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045650	TACAGTTTTGTCTTT[C/G]ACTTTAACCATGTTG	154214
rs778242770	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125073229	AATGATTCAGAGGTC[C/T]AGTAGGGCTGTTGGC	154214
rs778273251	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124984874	GATACTATAAACTGA[A/G]ACAAAAGACAATTCA	154214
rs778294427	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125029387	TATGGTTCCTCTACA[C/G]TAAACAGCATTTTAT	154214
rs778296535	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125043896	TACTAATAAGGAGAA[C/T]TATCCAAAGCCACCC	154214
rs778311402	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124991267	CTCGGACTCTTTGCT[C/T]TTTCTCACATCAAAC	154214
rs778326148	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125077267	CATGGAGCGTAGCCT[A/G]GGAAGGCAGGGGAAA	154214
rs778365426	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125052452	GCAAGGATCACTTGG[C/G]CACATTTGGACTGTT	154214
rs778384300	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030497	TATTGGGTAAATACA[A/G]TCATTCCAAATGGGA	154214
rs778405240	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125032470	CCAAATATATAAATA[C/T]ATATATATATTTCTT	154214
rs778409539	snp	C/G	1.65111e-05	0.0028732	splice-donor-variant	RNF217	GRCh38.p7	6:125076859	GAGGGTCAGTCTGTG[C/G]TGAGTGTCTGACATA	154214
rs778414208	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065768	TAAGAGTTGCTTTCT[C/T]TTTCTACAGCAAACT	154214
rs778435133	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125075934	ATGTATATATACCAT[A/G]CCACCACTGTATGGT	154214
rs778443748	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124970400	TGACAGAATGCCAAT[G/T]ATTGCACATGGGATG	154214
rs778477584	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125007827	GTGGATACCTAAAAT[A/C]ATGGATAGTACTGAA	154214
rs778482208	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090422	AACAAACATTTATAT[C/G]AATGTATATCTATTT	154214
rs778484191	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124988080	CTCCTATCAGGTCAG[C/T]GAAGGCATCAGATTC	154214
rs778499520	snp	A/G	1.6501e-05	0.00287232	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125076727	CTAATTTTTGTTACC[A/G]ATGTGGTGAGAGATA	154214
rs778535008	in-del	-/TG			intron-variant	RNF217	GRCh38.p7	6:125048091	TTCATCATTAAACTC[-/TG]TGGTTTATGTTAACA	154214
rs778549783	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000600	ATCCTCACATTAATC[A/G]GGTATTCTAGGAAAA	154214
rs778577325	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026358	TCCTGGTAGGGTCTT[C/T]ATCAGGAGTAACTGA	154214
rs778585138	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125022376	AAATTAACACATTAA[C/T]AAAAATAAGTAACAA	154214
rs778617399	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125028305	GAACAACACACAAAG[A/C]TAATTTGAGGACCCC	154214
rs778655292	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124966096	ACAAAGGGCTTAAAG[C/T]GGACAAAAGTAACAG	154214
rs778671197	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124980132	AAGGGATTTTTTGTT[A/T]GTTTGTTTTTAATGT	154214
rs778705277	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125029961	AGACATACCTGAGAC[C/T]GGGAAGAAAAAGAGG	154214
rs778707373	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125001820	ATTTTCTAATGCTGA[A/G]TGGAATGATTCAAAG	154214
rs778729550	snp	A/T					GRCh38.p7	6:124979285	GGAGTAGAAAAAGTT[A/T]GAACTTGGCTATTGT	154214
rs778761225	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124981309	GTTTCAGTTAATTTA[C/G]AAAGTTTATTTTGCG	154214
rs778776300	snp	A/G	2.04392e-05	0.00319675	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125082973	GCTAAGCTGGTTGGA[A/G]TAGGAGCGATACCAA	154214
rs778795153	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125069160	ACTTAACTTGAAACA[C/T]GAAATTTTCTGTAAC	154214
rs778798049	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125060608	AGCCACCATGCCTGA[A/G]TAATTTTTGTTTCTT	154214
rs778809994	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125043891	GTCAATACTAATAAG[A/G]AGAATTATCCAAAGC	154214
rs778859785	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125016897	CCAACAATCCTGCAC[A/G]TTCTGCACATGTATC	154214
rs778883090	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125070431	TCAAGGAATCTGTTT[C/T]CCATAGTGATTGTAC	154214
rs778890956	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125058340	CCACATATAAATATT[C/G]ACTTAAGACATTGAG	154214
rs778892841	snp	C/T	2.77543e-05	0.0037251	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124963018	GCGCCCGTCCCTCGC[C/T]AAGAGACAAGTCTTC	154214
rs778904157	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125073003	TGCTTGGCACATAAT[A/G]GGCTCTACGCAAAAA	154214
rs778937628	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967001	AGTGCAGTAGCTGCC[A/G]TCCAGTTTCTGATCG	154214
rs778942309	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125013446	GGGATGTTCATAAGA[G/T]ACCTGAATGATGCAA	154214
rs778978633	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125046992	ACAGTGGTGTTGAAG[A/G]CTAACTGAACATTAA	154214
rs779032091	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124999486	AGCTTTAAAATTGTG[G/T]TTCAAACTCATTGTT	154214
rs779032283	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125014766	GAACTCATTTTTGTG[A/G]TGAAAGGAAGTTATT	154214
rs779057544	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002717	GTCCGTGTGATTTTC[A/G]TGCTGGCTTATCAAA	154214
rs779108120	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124984827	ACTCAGCTTTATTCC[C/T]TCTAAGCAAAGAATT	154214
rs779109440	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125080392	CTTAAGAATAAAAAA[A/G]TTAGTATGTTTTGAC	154214
rs779109809	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124968827	AGCTTTTTATTAAGG[A/G]TTTGTGATGGACAAA	154214
rs779145675	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125004381	TTACCCTTGGATTGT[A/G]CCAGCACTGTCTAGC	154214
rs779167944	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124997076	TTTTTCATCATTTCT[A/G]TCAAAAAAGAATTTA	154214
rs779169807	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125049604	TGGGGATAGTAATAG[A/T]ACCTATGTCATAAGA	154214
rs779174706	snp	A/C	1.71522e-05	0.00292845	intron-variant	RNF217	GRCh38.p7	6:125057939	GATTTTTTTCTTACA[A/C]AGATCCAGTGCCCTA	154214
rs779271995	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125066355	CATAGAACCCGTCGC[C/T]CTCTGGACATGTCCC	154214
rs779276168	snp	C/T	3.93724e-05	0.00443674	intron-variant, nc-transcript-variant	RNF217	GRCh38.p7	6:125048257	GTTCTTTGTGATGAA[C/T]AGGTGAACATTTTTT	154214
rs779276642	snp	C/G	1.86333e-05	0.00305226	missense, intron-variant, nc-transcript-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124962718	TGGCTGCGGAAGCGA[C/G]TGGGGCTGCGCGGAC	154214
rs779297138	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125007808	ATACATTCCAAGACT[C/T]CCAGTGGATACCTAA	154214
rs779299238	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125035776	AGAAGCTTTTTCATT[C/T]GCCTTTTATATTTAC	154214
rs779300814	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976989	CCTGATACTTTGCTC[A/G]TTTTTTTGTTTGTTC	154214
rs779305160	snp	A/T			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961015	GCAACTGAGCCTCAG[A/T]CACACATATATGATG	154214
rs779327233	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125009112	CAGACGTGTTAGAAA[C/T]GTATGTATAAAGGGA	154214
rs779338970	snp	A/G			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967567	GATGCATATAACTTG[A/G]AATGTATACACCTGT	154214
rs779348984	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125038194	TGTTTTTGTTCAGAA[A/C]AACTGAACAGCATCT	154214
rs779353669	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125042046	CATATCTTGTTGAAC[A/T]CATGAAAAACTGTAC	154214
rs779414788	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124996487	ATCTTCTACCAATTC[A/C]TGGTTTTCTTTTTCT	154214
rs779424795	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125013205	TTTTTGGAGATTATA[A/T]TTTAGTGAGAAGAAA	154214
rs779446023	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125054184	AAAGGTACTGAATCT[C/G]GTTGCAAGAAATAGG	154214
rs779468197	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125057249	GGCACAATCTCGGCT[C/T]GACTGCAACCTCCGC	154214
rs779491477	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124986203	CCAGGCTGGCATTAG[G/T]CTTGATTTGTAACTT	154214
rs779512729	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124999254	ATTTTTAATCTGCCC[A/G]TGTCATGAGTTTCTA	154214
rs779525927	snp	C/T	4.47357e-05	0.00472926	intron-variant	RNF217	GRCh38.p7	6:125082429	ATTATGTAATAGATA[C/T]TATTATCTGTATTAT	154214
rs779535952	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042960	CTCGAGGTGGCCCAA[A/G]TAAGCCCCTTTTCTG	154214
rs779545498	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125031344	CTGCAGCTGGCTTGA[A/G]TTTTTCTGTAGAAAA	154214
rs779573273	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088290	TTAAGATTGTGAAAT[A/G]TTACCTTTTGGATGC	154214
rs779574047	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124999545	ACTGTACTTTAGGCT[C/T]ATAGACTGTAGTTCT	154214
rs779587363	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:124983474	TTAGTGGATTTATGT[C/T]CTCACTTGTCACTAA	154214
rs779597940	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965875	TCTTACACTTAAGTA[A/G]TTAAGTCAAGACAGA	154214
rs779617698	snp	C/G	1.67284e-05	0.00289205	missense, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081487	TGGGATTGGCACTAG[C/G]GGCCATAGCGGTTGT	154214
rs779662342	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125080320	GAGATCTTTTTAAAT[C/T]AGATATTTAAAACAG	154214
rs779725195	snp	C/T	1.67206e-05	0.00289137	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125081466	TTGCACCTCTAATTA[C/T]GGTTTTGGGATTGGC	154214
rs779750141	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125067976	TAAGGAGGTACTGAG[C/T]GACTGATTAAGTGAC	154214
rs779791015	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125065600	TGATGAGGGCTTCTG[C/G]AAAGGATGAAATCCA	154214
rs779809887	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124992523	TCTATAGCAAGATAC[C/T]GGATTCGGTTAGCTT	154214
rs779817413	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125032259	CCCATAATTCATTAG[G/T]GCAAAGATATGGGAT	154214
rs779847730	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125001487	AGATAAAGACGTAAT[C/G]ATATGTTTTGTCAAC	154214
rs779849330	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125051872	GGGCTATGCAAATCA[A/G]GGAAGAATTTTCCAG	154214
rs779881853	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088075	GCCCAGGCTGGTCTC[A/G]AACTCTTGGGCTCAA	154214
rs779885272	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041344	GACTTCCAGAATTCT[C/T]CCAACCTTCACTTTT	154214
rs779896129	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124993478	GCTTAGGAAATATGA[A/G]AGAATAAGATCATTC	154214
rs779960319	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125064310	TCATTGGCACTGTTT[C/T]TATGGTATGCCAAGC	154214
rs779971036	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125021270	AACATGGAAAAAGCT[-/T]TTTTTTTTTTTTTTG	154214
rs780003950	snp	A/G	4.32797e-05	0.00465167	intron-variant, missense	RNF217	GRCh38.p7	6:125082454	TATTATACAGTTGAG[A/G]AAATTAAGACTTACT	154214
rs780011096	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125023882	AAAAAGTCAAACTCA[C/T]AGAAGCAGAAAGCAG	154214
rs780016666	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125074111	CCTCCCAGTTCACCT[-/A]AACGATTTTGAATAC	154214
rs780027596	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125069028	CAAGGGAAGTGGTGT[C/G]GTAAAGAAGAAGGAA	154214
rs780062655	in-del	-/TGTGTG			intron-variant	RNF217	GRCh38.p7	6:125071489	CTGCCTACATATGTG[-/TGTGTG]TGTGTGTGTGTGTGT	154214
rs780074637	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124979998	AGAACGTCCTTGCAG[C/T]CTTTCTATTGAGACA	154214
rs780117094	snp	C/T	3.62522e-05	0.00425732	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045439	AGATCAGAAAGCAAA[C/T]ACAAAGTAAGCATTT	154214
rs780124221	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125027454	AACAGAATAATCTGC[A/G]ATTTCCTCCATATTG	154214
rs780192317	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125042938	TGCTTCCCAATAACA[A/G]GTGCCTCTCGAGGTG	154214
rs780201235	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125074595	TACAACAAGGTTTTA[-/T]TTTAAAGTAAAGAAA	154214
rs780212637	snp	C/T	3.306e-05	0.00406558	missense, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045296	TTGTCTATAACTTAA[C/T]GCATGAAGACTCCAT	154214
rs780213679	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125015415	AACAAATACACTAGG[A/T]TATTAATCACTACAA	154214
rs780213734	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125028469	GTGTATACAGTGTAT[A/G]TTTTGGAACTATACT	154214
rs780220728	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125071783	AGATAGAAGAAACTA[C/T]GAGTACTAACAATTC	154214
rs780277526	in-del	-/C			intron-variant	RNF217	GRCh38.p7	6:125077404	AATAAGTATCAAATG[-/C]CCTCAGTGCATACAA	154214
rs780308669	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125060142	ACTGAGTGAATTAAT[A/G]TTTGTTTTATACTGT	154214
rs780319208	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:125002059	TGAGCCCCAAACTCC[-/T]TAATGGATGGTATGC	154214
rs780355705	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124968715	CTGATACCTTTAGAG[C/T]GTGATTTTTCCCTCC	154214
rs780366432	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124973766	TTCTTTAATTACAAT[A/C]CCTGTTCTGGTTACT	154214
rs780398552	snp	A/T	1.86586e-05	0.00305434	synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	RNF217, RNF217-AS1	GRCh38.p7	6:124962805	AGCACCGGCGCAGCC[A/T]GCGGGACTGGCACTC	154214
rs780400060	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125053174	TCCAGCTTCACTGAA[C/G]CCTCTTTCCATGGCA	154214
rs780432052	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125030778	ACGGTGCAAGCTGTC[A/G]GTGGATGTACCATTC	154214
rs780458495	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975344	TATTAATTTATGTTC[A/G]TCTAAGTAGAGCTAT	154214
rs780459890	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092146	AATTAAGAGATTTTT[A/T]TTTTTAAGCAGTGAA	154214
rs780468910	in-del	-/TTTG	0.00724628	0.0597548	intron-variant	RNF217	GRCh38.p7	6:124971455	ACTGTTAAGTTTTTT[-/TTTG]TTTGTTTGTTTGTTT	154214
rs780469558	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124975576	GCTGGGACTATAGGC[A/G]TGCACCACCATGCCT	154214
rs780474331	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125021328	CTGGAGTGCAATGGC[A/G]CGATCTTGGCTCACT	154214
rs780490145	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125041700	CTTAGAGATTGCTTC[C/T]ATGATGTGTAGTTCA	154214
rs780499838	snp	A/T	1.65386e-05	0.00287559	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125058060	GTCACTGGGCCAGCG[A/T]AATTGAGCATGGGCA	154214
rs780504173	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125064584	TACTCAGATATCATC[A/G]AATTTTATGGTTCCT	154214
rs780526832	in-del	-/A			intron-variant	RNF217	GRCh38.p7	6:125026839	GAAAAAAATGAAAAC[-/A]AATTAAAATGAACTG	154214
rs780576202	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125024854	CGTAGATATCAGAAG[C/G]TTAGTATAGAGATCT	154214
rs780590726	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125040785	CAAGACTGATTCAAC[A/G]TATGCAAATCAATAA	154214
rs780592734	snp	C/T			intron-variant, utr-variant-3-prime	RNF217	GRCh38.p7	6:124967046	TGAGCTGACAGATTA[C/T]GAATCTTTAGCACCA	154214
rs780596181	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125065489	TACATAAATGCCAGC[C/T]CCACCATCTTTGTGA	154214
rs780611268	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007620	TTCAGTGCTTGGGGT[A/G]CAGACATCTTTTGTT	154214
rs780646995	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091450	GATGTATATAGGCTG[C/T]GTTTGCTACCTTAAT	154214
rs780660067	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125012029	ACTCATTGAACAAAT[A/C]TATACTGAATCTAAT	154214
rs780661147	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125007615	TTTTCTTCAGTGCTT[A/G]GGGTGCAGACATCTT	154214
rs780670523	snp	C/T	4.97088e-05	0.00498517	intron-variant, synonymous-codon	RNF217	GRCh38.p7	6:125082552	TGATATGCTATACTG[C/T]CTGAAACAAGTGTGA	154214
rs780688797	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125054524	CTTTGCCTCCATGAA[A/G]GCATCCTTTGTATCT	154214
rs780709894	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125055261	TTTAACTTATTTGTA[A/T]TCACTTGAGAGACTG	154214
rs780745426	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124995390	ATTGAATTATTTATT[A/T]ATTTAGTTTCATTAC	154214
rs780749142	in-del	-/T			intron-variant	RNF217	GRCh38.p7	6:124970063	AGAGAATGAAGTGGG[-/T]AGTGCTAAAAAGAAG	154214
rs780768470	in-del	-/CCTTT	0.000186585	0.00965699	intron-variant	RNF217	GRCh38.p7	6:125046682	TTTCTGGTCATGTTC[-/CCTTT]CTTGAGAGCAGCAGT	154214
rs780792166	snp	C/T	1.65811e-05	0.00287929	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057969	ACCTGCCAATTCGTC[C/T]GGTGTTTTAAGTGCC	154214
rs780816616	snp	C/G			upstream-variant-2KB, intron-variant	RNF217, RNF217-AS1	GRCh38.p7	6:124961603	TTGGAGGAGTAGATC[C/G]AAAGTGCTTTTTCGA	154214
rs780827661	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124970156	CCCTAAAGTAAAATG[C/T]TGTAAGAAGATACTG	154214
rs780846055	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002600	GACCACAGCCACCCC[A/G]TTTTCCTCTTCTTGC	154214
rs780865207	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998527	GTAGAAGGCCAGGTG[C/T]CGTGGCTCAAACCTG	154214
rs780900629	snp	G/T			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086585	AATACATTAGATTAT[G/T]TACGATTTAGTGATT	154214
rs780908768	snp	A/C			intron-variant, upstream-variant-2KB, missense	RNF217, RNF217-AS1	GRCh38.p7	6:124964285	CTATTCATCTTTCAA[A/C]ACCCTGTGTGTTCAG	154214
rs780927265	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125072525	AAAAGAGAAAGGCTA[C/G]AAAGTGCAAACTTAT	154214
rs780933866	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124990961	GTAGTCCTAGCTACC[C/T]GAGAGGGAGGTGGGA	154214
rs780942230	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125005473	TTTTGCAGGCAAGAG[A/C]ATAAACTTGATCTCT	154214
rs780963066	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125044868	GCAGTTCTTGCAGTT[C/G]GTGCATCATCTGAAT	154214
rs780996818	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124965576	AGACTCCTCTCAAAA[A/G]AAAAGAAGAATATAC	154214
rs781067123	snp	A/G	1.79735e-05	0.00299774	intron-variant	RNF217	GRCh38.p7	6:125045171	GAAAGAAAATAACCA[A/G]TGACGTTTTTTTCCT	154214
rs781085526	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026681	CAGTTAGGTGCTATA[C/T]AAGTCAGCTTTTTTT	154214
rs781095582	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082943	GCACTGGTAACATGC[A/C]GATGATTTCATCCAG	154214
rs781096449	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125066623	AAAATTTCAAACCAC[C/T]GTCCCCTACCTCAGT	154214
rs781101192	in-del	-/AATTAAAAAAAAAAAAAAGAATTCTA			intron-variant	RNF217	GRCh38.p7	6:125079434	CAAAAATGAATACTC[-/AATTAAAAAAAAAAAAAAGAATTCTA]AATTAAAAAAAAAAA	154214
rs781102423	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998976	AAGTGCCTTTTGTTG[C/T]CACTTTTTGTTTTCA	154214
rs781124582	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125003964	GTTTAAGCTTGTTGT[C/G]CAGTAGCCAAATGAT	154214
rs781182025	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125080157	ACATTCTTTTAAAAT[A/G]TATGTGCTTATATAT	154214
rs781205210	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:124975191	ACTCAGTATTCATGA[A/C]ACTCATGAGCTCTGA	154214
rs781220817	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124992195	TAGAATGCTCTAAAA[C/T]ATTAAGGAATAACTC	154214
rs781260447	snp	C/G/T	5.29482e-05	0.00514507	missense, stop-gained, utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125082911	AAAAAACAGAGAAAA[C/G/T]GATCACGGACAGGTA	154214
rs781267925	snp	A/G	0.000143168	0.00845953	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045466	ATTTTCACCAGAGCT[A/G]TGGGTTAGATGTCAC	154214
rs781272467	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125040528	CAGAGGAGCTAATAT[C/T]ATTCCTTCTGAAACT	154214
rs781296984	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125063495	TGTTTGTGGTGTTAT[C/T]ACAGTAATAATAACA	154214
rs781351399	snp	A/G	4.97632e-05	0.0049879	intron-variant, missense	RNF217	GRCh38.p7	6:125082560	TATACTGCCTGAAAC[A/G]AGTGTGAGTATCATA	154214
rs781359594	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125041575	TCTGAGCAGAGGCAA[A/G]TCAGACACCTTCTGA	154214
rs781361764	in-del	-/ATG			intron-variant	RNF217	GRCh38.p7	6:124991509	TATTATCTTCTAATA[-/ATG]ATGTGTTTTATTTAT	154214
rs781375239	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125083366	GTACCAACAAGCAAG[A/G]CCACTTTTCAGAAGA	154214
rs781418351	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124995124	TTGTCAGTTATTTAT[A/G]CCACCACCTTCTTCA	154214
rs781446708	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125026421	CTGGCACATACTAAA[C/T]GCTCAACAAATGTTA	154214
rs781474884	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125038395	TATGGTTTTAAAAAG[A/T]CTTCTTAATTTTTTA	154214
rs781537937	snp	C/T	1.65411e-05	0.00287581	synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125045336	GTACTTCTTGGAACT[C/T]GGCCGTATTGATTCC	154214
rs781548379	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125040742	AAAGCTTATCCACCA[C/T]GATCAAGTCGGCTTC	154214
rs781556509	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125070710	TTTGAGTTTCAGGAA[A/G]TTTTTTTAAAGCTTT	154214
rs781565152	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125074482	ATATTGTTCCATTAA[A/G]TTGCAGTTTTATATT	154214
rs781580443	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124973552	AGCCTGAATGAATGA[C/T]TGAAAATAAATTATA	154214
rs781620789	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:124987894	TGCGGTTTGTTGTGA[G/T]TTTAGATTGGATTAA	154214
rs781644597	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125063044	TAGTTTGTAGACTTA[C/G]TCATTACAAAACCAA	154214
rs781751226	in-del	-/AGG			intron-variant, upstream-variant-2KB, cds-indel	RNF217, RNF217-AS1	GRCh38.p7	6:124963727	CACAAGCTTGCTCAA[-/AGG]AGGAGAGGAAGAGAC	154214
rs781764932	in-del	-/TGTT			intron-variant	RNF217	GRCh38.p7	6:125043788	AAAAATAGAAAAAAG[-/TGTT]TGGGCACATATTTTT	154214
rs781777977	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125021179	TGGAGACAGCCTCCA[C/T]GTGGAGTTTAACTGT	154214
rs796123847	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124976487	GTTGGCCAGGCTGCT[C/G]TCAAACTCCTGACCT	154214
rs796130864	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125055444	AGAATCATGCATTGC[C/T]ATAATTGTCTTCATT	154214
rs796136872	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:124974808	TGTTTGTGGTATTCT[A/T]GTTTGTGTGGGTGAT	154214
rs796190420	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125017723	CCATTAACTTTGGAA[A/G]GTTATAATTACATAT	154214
rs796193753	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124987065	TACTAGCATGTATGC[A/G]CATTCATAATTTGGA	154214
rs796200333	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125080407	GTTAGTATGTTTTGA[C/T]AAACTTCCAACAAAT	154214
rs796227352	multinucleotide-polymorphism	ATA/GTG			intron-variant	RNF217	GRCh38.p7	6:125071534	GTGTGTGTGTGTGTG[ATA/GTG]ATATCTTATTACAGG	154214
rs796272717	in-del	-/AG			intron-variant	RNF217	GRCh38.p7	6:124979043	CCAGAAGAAACCAAT[-/AG]AGAGAGAGAGTGTAA	154214
rs796294518	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125037045	CAAGACTGATTTTTT[A/T]AATGGATATTAAACC	154214
rs796319409	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:124974498	ATATTTTAGGTAGTT[C/G]CACTGTAATTGAAAT	154214
rs796359008	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125079411	AAACAAAAACAATGG[A/C]GCCTTCTCCAAAAAT	154214
rs796426952	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125052613	TGGAGAATTTCTTTC[C/T]ATTGCCACCATCTGA	154214
rs796429789	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125021731	TTTTCTGTTTTCCCA[A/G]TTTCCTTTATAAAGT	154214
rs796444460	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125077227	ATCCTCCACTCATTC[A/T]TGGAGGACCTGCAAT	154214
rs796537826	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125016205	GTTCTTTCATTATTC[G/T]TTGTACTTTTCCAGG	154214
rs796541485	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124977044	TCATACATGCTTTTC[C/T]CTTTAAAATCACTAG	154214
rs796560072	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124978800	CCTGACCAAGAGGAA[C/T]AAGGTACGTGGACAC	154214
rs796592608	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:125054323	CCTCAATTAGTGAGG[C/T]TTAGTCTAAGGCTCC	154214
rs796598504	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125035727	AATCTTACTCTTTCC[A/C]AAGGTCATGAAGATG	154214
rs796617657	in-del	AA/GAAAG			intron-variant	RNF217	GRCh38.p7	6:124984557	AAAAAAAAAAAAAAA[AA/GAAAG]AAGAAAGAAAGAAAA	154214
rs796639339	snp	A/T			intron-variant	RNF217	GRCh38.p7	6:125035982	GTTACATAGGTATAC[A/T]TGTGCCATGGTGGTT	154214
rs796671512	in-del	-/TT			intron-variant	RNF217	GRCh38.p7	6:125007250	TTTTCACTTTGAGCA[-/TT]TTTTTTTTTTTGAGA	154214
rs796695007	multinucleotide-polymorphism	GT/TA			intron-variant	RNF217	GRCh38.p7	6:125052325	TGTGTGTGTGGTTTT[GT/TA]TTGTTTTGTTTTGTT	154214
rs796774484	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125000953	GGAAGTATGATGTAT[A/G]AGAAATGTCTTTCAA	154214
rs796776432	in-del	-/AT			intron-variant	RNF217	GRCh38.p7	6:125060381	CACACACACACACAC[-/AT]ATATATTTGTACCCT	154214
rs796804582	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:124976873	TTGTTCTTAGTTTTT[A/G]TTATATCACCTTTTG	154214
rs796807992	snp	C/T			intron-variant	RNF217	GRCh38.p7	6:124998854	TTATAAGCACCTGTA[C/T]GGTTGTAAACATGTA	154214
rs796836294	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125002644	TGTCACGCTGGCCCC[A/G]TATGTTCCTGTTTGA	154214
rs796840799	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125014275	GAAATAGTGATAGCA[A/G]TCACTCACAGTTATT	154214
rs796861636	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125071484	AGCATCTGCCTACAT[A/G]TGTGTGTGTGTGTGT	154214
rs796862914	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime	RNF217, RNF217-AS1	GRCh38.p7	6:124964583	ATGCTTGGGTCTAGA[C/T]TGAAAGTGTGTACAG	154214
rs796914271	snp	C/G			intron-variant	RNF217	GRCh38.p7	6:125023847	AATGCCACATGGTCC[C/G]CCTTTATATATGGAA	154214
rs796926625	snp	G/T			intron-variant	RNF217	GRCh38.p7	6:125019507	TATGTTATTCTTATA[G/T]GACTATTACATTCCT	154214
rs796941409	snp	A/C			intron-variant	RNF217	GRCh38.p7	6:125026413	AATAGTGCCTGGCAC[A/C]TACTAAACGCTCAAC	154214
rs796975808	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125038206	GAAAAACTGAACAGC[A/G]TCTTTTTCAGTGATA	154214
rs796979176	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125019354	AGAACTTACAACTCT[A/G]CTATCTTTCTTACCA	154214
rs796985648	snp	A/G			intron-variant	RNF217	GRCh38.p7	6:125011635	TACATTTTTAATTGG[A/G]TTAGATCCCATAGTT	154214
rs797021562	in-del	-/G			intron-variant	RNF217	GRCh38.p7	6:125049963	AAACATGACTCAGGA[-/G]GTGATTTGGTGGAAG	154214

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