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

RC3H2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs372223304	snp	C/G	4.96997e-05	0.00498472	missense	RC3H2	GRCh38.p7	9:122890378	CAGACAACTGCTGAG[C/G]GTTCTGGTGCTGTAA	54542
rs372230634	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122888942	GCATGCCCATGACTA[C/T]TGGATGAGAGTACCT	54542
rs372334202	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122862443	CATCCACAAGGCCCT[G/T]CCTTCCTTGCTATCC	54542
rs372403171	snp	C/G	2.36706e-05	0.00344017	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897529	GAAGCTGGATGCTCG[C/G]GTTAGCAGTCTAGCA	54542
rs372447693	snp	G/T	1.6696e-05	0.00288924	missense	RC3H2	GRCh38.p7	9:122854235	TGGAATGCTTTCTAT[G/T]ACCAGATAAATCAGT	54542
rs372603256	snp	A/T	0.000167986	0.00916322	intron-variant	RC3H2	GRCh38.p7	9:122865701	GAATATTTCACTAAA[A/T]CTTACTCAAGACAAA	54542
rs372664374	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122850626	TTTTTTGTATTTTTG[A/T]AGAGACAGGGTTTCA	54542
rs372815423	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122875103	GTCTCCCAAATTATC[C/T]TGATGTGAAATTCTG	54542
rs372872164	snp	A/T	3.44465e-05	0.00414995	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879752	TGTAATAAATGTACT[A/T]ACCTGAGGGGTCTCA	54542
rs372885100	snp	C/T	1.66045e-05	0.00288132	missense	RC3H2	GRCh38.p7	9:122893004	CCTAGATTACTTAAC[C/T]TAATTGACTGATGAT	54542
rs372944811	snp	A/G	0.000115935	0.00761277	synonymous-codon	RC3H2	GRCh38.p7	9:122857998	AGGAAGAGTTGAAGA[A/G]ACAAGAGGTGCTTTC	54542
rs372949080	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122878563	ACATGAGCCACCGCG[A/C]CCAGCCCCCTGACAG	54542
rs372952802	snp	C/T	0.000165986	0.00910854	intron-variant	RC3H2	GRCh38.p7	9:122851458	AAAATACTGATTTTG[C/T]TCTCCCTCTCCCTCT	54542
rs372968566	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122851786	TTGCAGACGGAGTCT[C/G]GTTCACTCAGTGCTC	54542
rs372996333	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122885973	GCTCACTGCAACCTC[C/T]GCCTCCTAGGTTCAA	54542
rs373061909	snp	A/G	3.31549e-05	0.0040714	intron-variant	RC3H2	GRCh38.p7	9:122854091	TTGCTCTTGGCCTAT[A/G]TGAGGAGGGAAAAAA	54542
rs373194978	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903991	AAGGCTGCACTGGCT[A/G]ACATTTGTTTCTTTG	54542
rs373202822	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878359	GCAAGCTCCACTTCC[C/T]GGGTTCAGGCCATTC	54542
rs373218840	snp	A/C/G	1.65844e-05	0.00287957	missense	RC3H2	GRCh38.p7	9:122858994	TAATGATCGGCATAT[A/C/G]GCATGGAAGCAGGTG	54542
rs373232167	snp	C/T	0.0652144	0.168387	intron-variant	RC3H2	GRCh38.p7	9:122852185	ATGCCTCTGCCCGGC[C/T]GCCACCCCGTCTGGG	54542
rs373385496	snp	C/T			intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880317	TAGACACTTAGAAAA[C/T]TTATAAGCTGTATTA	54542
rs373393847	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122897927	TTGGACTGCTGGGCG[G/T]TTTTTTTGTTTTGTT	54542
rs373441546	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122870458	ACAAGGTTGCTCTAG[A/C]AAGCAAAAAATAAAG	54542
rs373442491	snp	A/T	1.65611e-05	0.00287755	missense	RC3H2	GRCh38.p7	9:122865427	ACTTTCTTCACGGTC[A/T]CCAGAGCTCTTAAGG	54542
rs373459909	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122891619	CTCCTTTAAAACACA[C/T]TATTTGGCTTACTAA	54542
rs373481161	in-del	-/TTT			intron-variant	RC3H2	GRCh38.p7	9:122891013	ACCAAATCTGCCCCA[-/TTT]TTTTTTTTTTTTTTT	54542
rs373492115	snp	A/G	1.70772e-05	0.00292204	intron-variant	RC3H2	GRCh38.p7	9:122865686	AATCAACAGATTGGT[A/G]AATATTTCACTAAAT	54542
rs373518954	snp	A/G	4.61318e-05	0.00480248	intron-variant	RC3H2	GRCh38.p7	9:122855164	AACATATCAGGCTAG[A/G]TATTATCTAAATGGA	54542
rs373631483	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122898737	CTGGACAAAAAGAGC[A/G]AAACTTAATCTCAAA	54542
rs373687789	snp	C/T	0.0178098	0.0926698	intron-variant	RC3H2	GRCh38.p7	9:122879264	CAGGGCGTGGTGGCA[C/T]TTGCCTGTAATCCCA	54542
rs373702578	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122868441	TGATCTGTGACCTTA[C/T]CCCCAACCCTGTGCT	54542
rs373726861	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122877139	GCAGTGGTGTGAACA[C/T]ACTCACTGCAGCCTT	54542
rs373818143	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122899987	CATAAGTGTGGGGCT[G/T]GGGGTGGGGGAGTTT	54542
rs373856957	snp	C/G	2.10537e-05	0.00324445	intron-variant	RC3H2	GRCh38.p7	9:122849839	TGAGAAAAAAGAAAT[C/G]ACATTAAAAACAAAT	54542
rs374013917	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850377	TATTTTTGGCAGTAA[G/T]TATTCAAAATGGCAG	54542
rs374047636	snp	A/G	3.3145e-05	0.0040708	missense	RC3H2	GRCh38.p7	9:122858721	GGCTGACAAGCCACC[A/G]AATAATATCCATCTA	54542
rs374121874	snp	A/C/G/T	0.000199541	0.00998673	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879905	AGGGCATGGGGGTTG[A/C/G/T]GGGGGAAGAATGTTA	54542
rs374122074	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861722	CCTCAAATTAGAACA[A/G]TCATTTTAAAGGTAG	54542
rs374134910	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892203	TGCAGCCTCAACTTC[C/T]TGGGCTCATGTGATT	54542
rs374216611	snp	C/T	1.91027e-05	0.00309047	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880308	ATTCATCATTAGACA[C/T]TTAGAAAACTTATAA	54542
rs374218952	snp	C/T	1.65633e-05	0.00287774	synonymous-codon	RC3H2	GRCh38.p7	9:122851194	TAGCAACTGATCATT[C/T]TGAGAACTGATACCA	54542
rs374224144	snp	C/T	0.000711856	0.0188526	synonymous-codon	RC3H2	GRCh38.p7	9:122859993	AATGTTTTCAGAATG[C/T]GGAGGATATACTGGT	54542
rs374282098	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863063	CAAGAGAAACCTGTA[C/T]CCATTAGCATTCATT	54542
rs374284481	snp	C/T	1.65649e-05	0.00287788	synonymous-codon	RC3H2	GRCh38.p7	9:122853991	CTTGCTTAAAAGGTT[C/T]AAGGTAAGGTGACGG	54542
rs374287508	snp	A/G/T	3.32167e-05	0.00407522	intron-variant	RC3H2	GRCh38.p7	9:122855435	ATAAAAGGACTGTTG[A/G/T]CAATTACTTCAGCTA	54542
rs374296708	snp	C/T	1.65644e-05	0.00287783	missense	RC3H2	GRCh38.p7	9:122865596	TGTTGTTTACACCAA[C/T]TTTATTTAGAAGAGG	54542
rs374325703	snp	C/G			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853615	AAATTAGCTGGGCAT[C/G]GTGGTGGGTGCCTGT	54542
rs374335919	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906589	TTAAACTCAAGGCAC[C/T]TTCCAATGTGAAATC	54542
rs374392591	snp	C/T	3.51512e-05	0.00419218	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879724	CTGAGTTAGAGACAA[C/T]AGCAGTCAGAAATGT	54542
rs374434614	in-del	-/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122878989	CTCGAACTTCTGGCC[-/T]CAAGTGATCCACTCA	54542
rs374443328	snp	A/G	5.67038e-05	0.00532435	intron-variant	RC3H2	GRCh38.p7	9:122897236	AATGGCAAAAATAGT[A/G]ATTATTTTTGCACCA	54542
rs374458490	snp	C/T	8.29428e-05	0.0064393	intron-variant	RC3H2	GRCh38.p7	9:122854144	AGCTTTCAACTGTCA[C/T]TCTATTTCTCAAAAA	54542
rs374485179	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122866330	GGACTGGCAATTTGA[A/T]TTTGGATTCCATTTA	54542
rs374580900	snp	C/G	0.000165986	0.00910854	intron-variant	RC3H2	GRCh38.p7	9:122859114	TATCCTTGAAAATTG[C/G]AAAGAGGAATATTTA	54542
rs374616016	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122897659	AGTCAACTATTACAG[C/T]TTCAGACCTAAAATA	54542
rs374652407	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122885216	AAGGAAAGGAGCATA[A/G]AACAAGCAACCTACT	54542
rs374715315	snp	C/G	0.000319949	0.012644	missense	RC3H2	GRCh38.p7	9:122858956	GAGAAGAATTCATTC[C/G]ATCTCGAGGGGAAAA	54542
rs374765186	snp	A/C	1.76512e-05	0.00297074	intron-variant	RC3H2	GRCh38.p7	9:122858646	GCTGTTAATGACTAC[A/C]TTATAGTAGCATCTT	54542
rs374775824	snp	A/C	0.000165986	0.00910855	synonymous-codon	RC3H2	GRCh38.p7	9:122897315	AAGTGCGAAGTTGAC[A/C]GGAAGTACATCAATA	54542
rs374834754	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122877537	CAACCCCCTTGCTGT[C/T]GCAAATCTCGGCACA	54542
rs374859885	snp	C/T	0.00123691	0.024838	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897525	TGTGGAAGCTGGATG[C/T]TCGGGTTAGCAGTCT	54542
rs374874917	snp	A/G	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122861196	CTTAACTCCTTTTAA[A/G]AAGTCAAATTTCGGC	54542
rs374882710	snp	C/T	1.65952e-05	0.00288051	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879807	ATGAAGTCCACAAGG[C/T]CATGAACTACTGTTT	54542
rs374959065	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122890175	TAACAACAACAACAA[A/C]AACAAATTTATCTTT	54542
rs375030052	in-del	-/TGTTT			intron-variant	RC3H2	GRCh38.p7	9:122885886	TGTTTTGTTTTGTTT[-/TGTTT]GTTTTGTTTTGTTTT	54542
rs375141134	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122891255	CTCAAATTCCTGACC[C/T]CAAATGATCTGCCCG	54542
rs375186135	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122888771	CCAGATGTTTGCTAT[C/T]ACAAATAGTGCTTTT	54542
rs375190526	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122868600	CCCAGGGACACAAAC[A/G]CTGCGGAAGGCCGCA	54542
rs375242961	in-del	-/ATA	0.00676609	0.0577691	intron-variant	RC3H2	GRCh38.p7	9:122896638	ATCACTAAACATACT[-/ATA]ATATACCTATTACTG	54542
rs375280153	snp	C/T	0.00874735	0.0655527	intron-variant	RC3H2	GRCh38.p7	9:122851890	GGCCTCCCAAAAAGC[C/T]GAGATTGCAGCCTCT	54542
rs375439611	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889009	AGATTCTGCCAATCT[C/G]ATAGGTGAGAAATGG	54542
rs375489482	snp	A/T	0.000169986	0.00921759	intron-variant	RC3H2	GRCh38.p7	9:122851273	TATGAAAGTATTTTA[A/T]AAATTTTCAATCAAA	54542
rs375549535	snp	C/T	0.00358779	0.0422022	intron-variant	RC3H2	GRCh38.p7	9:122868322	AAGGTGGGGAAAAGA[C/T]TGAGAAATCGGATGG	54542
rs375589958	snp	C/T	3.31252e-05	0.00406958	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880724	GCATCATGTTCTCTG[C/T]GTAATGCTTCATAAC	54542
rs375619679	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122888360	AAATATTTAAAGTTG[C/T]TTTATAATTACATAA	54542
rs375694288	snp	C/T	6.62712e-05	0.00575597	missense	RC3H2	GRCh38.p7	9:122854576	TCGTTGCCATATGAA[C/T]TCCACCTTGAATCAA	54542
rs375753611	snp	C/G	0.000167986	0.00916323	missense	RC3H2	GRCh38.p7	9:122892920	TTACCTTTACCTCCA[C/G]TTAGTGGTTTTAAGT	54542
rs375802220	snp	A/C	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122859593	GCAGACGTTAAAGAC[A/C]TCTTTCAAAATCTAT	54542
rs375822652	snp	A/G/T	1.65647e-05	0.00287786	missense	RC3H2	GRCh38.p7	9:122857955	CACTGAACAGAGGAG[A/G/T]AGGTGGTGTTGGTGA	54542
rs375871590	snp	A/G	3.31862e-05	0.00407333	missense	RC3H2	GRCh38.p7	9:122857927	ACCTTTCTTACATCC[A/G]CACGAAAGTCTACAC	54542
rs375937053	snp	A/C	3.48712e-05	0.00417545	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880272	TGAATTAAATTTTCA[A/C]CTCAGAATCTGCCCT	54542
rs375958717	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122903534	ATATGAACAAAGGAC[G/T]TAAGTCTTCTTACAT	54542
rs375966998	snp	C/T	3.31219e-05	0.00406938	missense	RC3H2	GRCh38.p7	9:122865398	CATTCTGACCATTAG[C/T]GCCAACCTTTCCCAC	54542
rs375994980	snp	A/G	0.000167986	0.00916322	intron-variant	RC3H2	GRCh38.p7	9:122855404	GTCCAGGTCCTATGT[A/G]AACCAAAGAAAATCA	54542
rs376071945	snp	C/T	0.000167986	0.00916322	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880130	GGAGACTGTAGCTAA[C/T]AAACAGAAATGAGAA	54542
rs376103984	in-del	-/TCC			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905299	GGGGCCTCCTCCTCC[-/TCC]CTCCACCTCCGCCTC	54542
rs376168225	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122852259	GGAGACCCTCCGCCC[A/G]GCAGCCGCCCCGTAT	54542
rs376168582	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122856711	AATAAGGAATACTTA[C/T]AGGACCAGAATACTA	54542
rs376172390	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122877595	GAGGCTACAAAAATG[C/G]GAACACATTCAATGA	54542
rs376175475	snp	A/G	1.92739e-05	0.00310429	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849596	AAATGCTTCCATGGT[A/G]TGGTCACAAATTTGA	54542
rs376226809	in-del	-/G			intron-variant	RC3H2	GRCh38.p7	9:122877733	AACTAATATTCCATT[-/G]TTTCCTGTTGTGAGT	54542
rs376346622	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122853097	CTCCAACCCTGTGCT[C/G]TCTGAAACATGTGCT	54542
rs376409900	snp	C/T	5.16151e-05	0.00507985	intron-variant	RC3H2	GRCh38.p7	9:122857879	ATTTGAAGTCAGCTG[C/T]TTGACCTATCCCTGC	54542
rs376421654	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867137	CCCGGCAACCGCCCC[A/G]TCTGAGAAGTGAGGA	54542
rs376530725	snp	C/T	6.63691e-05	0.00576022	missense	RC3H2	GRCh38.p7	9:122858998	GATCGGCATATGGCA[C/T]GGAAGCAGGTGGGAG	54542
rs376585569	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122866380	CCCTCCCCCTCCCCC[C/T]TCCCTCTCCCCACGG	54542
rs376591203	snp	A/G	6.62383e-05	0.00575454	synonymous-codon	RC3H2	GRCh38.p7	9:122858867	GATGCGCCTGCTGTC[A/G]TACACAGGAGCATAC	54542
rs376625924	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122894056	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	54542
rs376680596	snp	C/T	4.98227e-05	0.00499088	missense	RC3H2	GRCh38.p7	9:122893008	GATTACTTAACTTAA[C/T]TGACTGATGATCTGG	54542
rs376723673	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122895160	TAAATGGTAGCTAGG[-/T]TTTTTTTTTTTTTTT	54542
rs376846500	snp	A/G	1.66054e-05	0.00288139	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879881	AACAGCGTCTAAAAT[A/G]AGCCACCAAGGGCAT	54542
rs376855983	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899018	GTAGTCACATTCAAA[A/G]AGAAAAAATATATAA	54542
rs376885100	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122867457	GTCCAGGAGGGAGGT[G/T]GGGGGGTCAGCCCCC	54542
rs376899922	snp	C/T	0.000165986	0.00910855	missense	RC3H2	GRCh38.p7	9:122855190	ATGGATTACCTGATA[C/T]ACTGATGGGCTTAGT	54542
rs376931545	snp	C/T	3.32718e-05	0.00407858	intron-variant	RC3H2	GRCh38.p7	9:122858098	CCACAAGGTTCCTAA[C/T]GGGGGATAAAAGAAA	54542
rs376932615	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861856	CTAAGGAACTGTGGG[C/T]AATAAAAGTAGGTAC	54542
rs376995909	snp	A/C	1.96636e-05	0.0031355	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853846	AAGCAATCAATCATC[A/C]ATCAGAGATAGGCAC	54542
rs377000605	snp	A/C	1.65611e-05	0.00287755	missense	RC3H2	GRCh38.p7	9:122865461	TGTCAGTACTACGTG[A/C]GATTAGCTGGGAAAC	54542
rs377050254	snp	C/G	0.000201501	0.0100354	intron-variant	RC3H2	GRCh38.p7	9:122890289	ATAGCTAATAAAAAA[C/G]GTAAGATAGTAACCT	54542
rs377055741	snp	A/C	5.00471e-05	0.00500211	intron-variant	RC3H2	GRCh38.p7	9:122877430	CATTCCCATAAAAAT[A/C]AAAAATTAAACCCAT	54542
rs377060593	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122850534	CACTGTCTCCGCCTC[C/G]CGGGTTCAAGCGATT	54542
rs377061075	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122899240	CCCAAGTAACTGGGA[A/C]GGCACCCACCATCAT	54542
rs377111637	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898697	GAGATTGCAGTGAGC[C/T]GAGATCACGTCATCG	54542
rs377157832	snp	G/T	0.000347939	0.0131852	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879941	AATTCTCTTGTGTTA[G/T]TCACCTCAAAAGTAG	54542
rs377163052	snp	C/T	0.000161538	0.0089857	intron-variant	RC3H2	GRCh38.p7	9:122890272	GGCATCCTCAAGCCC[C/T]AATAGCTAATAAAAA	54542
rs377198590	snp	C/T	0.0256215	0.110247	intron-variant	RC3H2	GRCh38.p7	9:122851611	GCCTGATTCTCCTGC[C/T]TCAGCCTGCAGAGTG	54542
rs377288600	snp	C/T	0.000159987	0.00894248	missense	RC3H2	GRCh38.p7	9:122858026	TTCTGAGTGTGGTAC[C/T]GTGCCCACTGATCTG	54542
rs377308173	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904628	TCCCCATCCTGGGAG[A/G]TTAAGCCCTCCCAGG	54542
rs377334540	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122896993	ATCACGCCACTGCAC[A/T]CCAGCCTGGGTGACA	54542
rs377349398	snp	A/G/T	0.000182639	0.00955449	missense	RC3H2	GRCh38.p7	9:122849694	TCTTCAGACATAACA[A/G/T]GAGTTTTCAGAATGA	54542
rs377369771	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122868053	CCCAGCCAGCCGCTC[C/T]GTCCGGGAGGGAGGT	54542
rs377429026	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122891676	GACACTCTCAGTCCA[C/T]GCTCTTTAGATAGCT	54542
rs377490235	in-del	-/CTCTCC	0.0300682	0.11887	intron-variant	RC3H2	GRCh38.p7	9:122851458	AAAATACTGATTTTG[-/CTCTCC]CTCTCCCTCTCCCTC	54542
rs377501742	in-del	-/TA			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906925	TTCCACCCTACTGTG[-/TA]TATATATATATACAC	54542
rs377562011	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122872036	TCTTGCCTCAGCCTT[C/T]CAAAGTATTGGAATT	54542
rs377598996	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892175	TGAGTGCAGTGGCAC[A/G]ATCACAGCTCACTGC	54542
rs377606794	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867914	GTCAGCCCCCCGCCC[A/G]GCCAGCCGCCCCGTC	54542
rs377669334	snp	C/T	1.71381e-05	0.00292724	missense	RC3H2	GRCh38.p7	9:122859048	TTGGACCTCACAAAG[C/T]GAGGAACACAGGGAG	54542
rs377732580	snp	C/T	3.3129e-05	0.00406982	missense	RC3H2	GRCh38.p7	9:122854004	TTTAAGGTAAGGTGA[C/T]GGCCTTCATCCAGGG	54542
rs386738372	multinucleotide-polymorphism	ATG/GTA			intron-variant	RC3H2	GRCh38.p7	9:122886225	TCATCCACATGCAGC[ATG/GTA]TATCAGTATTTATTC	54542
rs397695861	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122861523	AGAAAAGAAAAAAAA[-/A]CCATATATATATGGC	54542
rs397732728	in-del	-/A	0	0	intron-variant	RC3H2	GRCh38.p7	9:122857829	CCAAACCACTGCAAA[-/A]TATCCAACATAGCTA	54542
rs397834444	snp	A/C/G			intron-variant	RC3H2	GRCh38.p7	9:122870405	aaacaaacaaacaaa[A/C/G]aaaaaaaaaacaaca	54542
rs397894679	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122891014	CCAAATCTGCCCCAT[-/T]TTTTTTTTTTTTTTT	54542
rs398012155	in-del	-/G	0	0	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905889	CCAAAGTGGGGGGGG[-/G]AGGGGGGGAAGAAAG	54542
rs527242623	snp	C/T	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122898533	GGTGGGAGGATCACC[C/T]GAGGTCAGGAGCTTG	54542
rs527261580	snp	A/G	3.39455e-05	0.00411966	intron-variant	RC3H2	GRCh38.p7	9:122854664	AAGTGAAAAATCAGT[A/G]TACTGAGGTGAATGT	54542
rs527355494	snp	A/G	1.65663e-05	0.002878	synonymous-codon	RC3H2	GRCh38.p7	9:122854051	CATGGCCAAAGCATT[A/G]GCCTCTCTCTGAAGA	54542
rs527465629	in-del	-/CCT	0.0130999	0.0798644	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905288	AAGGCCGCGACGGGG[-/CCT]CCTCCTCCTCCCTCC	54542
rs527478785	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884917	CAGGAATATCAGTGT[A/C]ATGAAAGGCAAAGAA	54542
rs527485365	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881516	AGAATTTTTAAAAGA[G/T]AAACAAGTGGTGAAA	54542
rs527528454	snp	A/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122884298	ACTCCGTCTCTAAAA[A/T]AAAAATTAAACACAC	54542
rs527590855	in-del	-/A	0.0023933	0.0345097	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907024	TACATATAAGTATAT[-/A]TACACATATAAACAT	54542
rs527608067	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898970	TTACCAACCCAAATA[C/T]ATTAGTTCCACAGAA	54542
rs527673272	in-del	-/TCTC	0.000111901	0.00747916	intron-variant	RC3H2	GRCh38.p7	9:122875262	CACACACACTTATCT[-/TCTC]TCTATCACAATGCTG	54542
rs527732148	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906600	GCACTTTCCAATGTG[A/G]AATCAGATGCCCAAC	54542
rs527733353	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122904234	GAATTAAAAAGGGAA[A/C]CCAAGGGTTATGAAA	54542
rs527746587	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122899630	TTAGTTTCCTTCCAA[C/G]TTTAGAGATAAGCAC	54542
rs527751153	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878430	CGCCTGCCACCACGC[C/T]CGGCTAATTTTTTGT	54542
rs527751171	snp	A/G	0.00953873	0.0683987	intron-variant	RC3H2	GRCh38.p7	9:122870380	ACTCTGTCTCCAAAA[A/G]CAAACAAACAAACAA	54542
rs527815562	in-del	-/TTT			intron-variant	RC3H2	GRCh38.p7	9:122869579	TTTTTTTTTTTTTTT[-/TTT]GAGGCGGAGTTTTGC	54542
rs527839542	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122900983	ATAAAACAGGAAGCA[C/T]AATAGGCATCTCTTA	54542
rs527861637	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857144	CGTGGAACCTGGGTG[C/T]TGGGTACATGGAGTT	54542
rs527869648	snp	A/G	4.99272e-05	0.00499611	synonymous-codon	RC3H2	GRCh38.p7	9:122849672	AGGTTTTAAAAAGTC[A/G]TTTTTATCTTCAGAC	54542
rs527929178	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900116	CAATAGTCCTTAGTA[C/T]AGTTTTATGTTACAA	54542
rs527943117	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856347	AGCCTCGACTTCCCA[A/G]GCTCAGGTGATTTTC	54542
rs528033569	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863724	CTAAAATCTTGCCCA[A/G]GGAAGATTGTAAAAG	54542
rs528082422	snp	C/T	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122866094	AAGAGCTGAAGCCAT[C/T]TTCTGTTGTTACCAA	54542
rs528104143	snp	A/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122873843	ATTTTTTTGAGACGG[A/T]ATCTTGCTCTGTCGT	54542
rs528105949	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881782	CTCTCGCTTTGGCCT[A/C]CCAAAGTGCTGGGAT	54542
rs528138444	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122892806	AGGCATTTCTCAAGC[A/C]AACTCCTTTTCCATA	54542
rs528278520	snp	A/G	0.00676609	0.0577691	intron-variant	RC3H2	GRCh38.p7	9:122852324	CCGTCTGAGAAGTGA[A/G]GAGCCTCTCTGCCTG	54542
rs528320250	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903828	TTCAAAAATTGAACG[C/T]GGAAGTAAACAACGT	54542
rs528342253	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122859798	GAAGGAAAAAAACTT[A/C]TGAGTCACATAGTCA	54542
rs528379187	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122866843	CCGTCTGGGAAGTGA[A/G]GAGCGTCTCTGCCTG	54542
rs528491489	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122882771	TGTATCTGAGATAAC[A/G]TGTAGGCCATTTTCA	54542
rs528511431	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890010	AGCCGGGTATGATGG[A/C]GTGTGCCTGTAGTCC	54542
rs528621249	snp	C/T			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853728	TTGCACTCCAGGCGA[C/T]AGAGCAAGATTCCAT	54542
rs528684986	snp	C/G/T	1.65644e-05	0.00287783	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880739	CGTAATGCTTCATAA[C/G/T]TCCGAAATTCCTCCT	54542
rs528726374	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876227	GGCTGGATGGCTAAA[C/T]TGGGTACACGAGGTG	54542
rs528733976	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862724	ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA	54542
rs528797677	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883482	TATAGTGGCCCATTA[C/T]CCATAATTTATATTT	54542
rs528926029	snp	A/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122866924	TGGAAAGTGAGAAGC[A/G]TCTGCCCGGCCGCCA	54542
rs528962764	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874613	GACCTGACCTCCCGA[C/G]TTCAAGCAATCCTCC	54542
rs529110528	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122861255	TAGCACTTTGGGAGG[C/T]CGAGGCAGGCAGATC	54542
rs529112287	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122859574	TTTATTAACTTTTTT[A/G]GGAGCAGACGTTAAA	54542
rs529130581	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122853105	CTGTGCTCTCTGAAA[A/C]ATGTGCTGTGTCCAC	54542
rs529131289	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905306	CCTCCTCCTCCCTCC[A/T]CCTCCGCCTCCTCCT	54542
rs529157263	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122904666	TTGGCCGGGGTTCCT[A/G]TTTACCACTCAGATC	54542
rs529171638	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892452	GTCTTGCTCTGTCGC[C/T]CCAGGCTGGAGTGCA	54542
rs529219099	snp	C/T	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122860703	ACAGGCATCAGCCAC[C/T]GTGCCTGGCCATTAC	54542
rs529244129	in-del	-/CAA			intron-variant	RC3H2	GRCh38.p7	9:122870413	AAACAAACAAACAAA[-/CAA]AAAAAAAACAACAAA	54542
rs529283041	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884066	TTGGGAGGCCAAGGC[A/G]GGCGGATCACCAGGT	54542
rs529300414	snp	C/T			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853499	GCTCACACCTGTAAT[C/T]CTAGCACTTTGGGAA	54542
rs529404119	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122887797	TCACCCAGGCTAAAG[G/T]GAAGTGGCATGATCT	54542
rs529428592	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884022	AAATTAGGCCGGGCG[C/T]GGTGGCTCACGTCTG	54542
rs529585258	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869702	GGAGTACAGGTGCAC[A/G]TTATAGGCGCGCGCC	54542
rs529603012	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876751	AAAAATTGGATAATA[A/G]TATTAAACCTTACAT	54542
rs529656579	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887123	TAATGGGTTTAACAG[C/T]CACAAATAATTCTTG	54542
rs529688062	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122879451	AGAAATTCAATACAG[A/G]AAAAAAATGACAATT	54542
rs529763235	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893724	CAAAATTAAAGAGTG[A/G]AGAAAAAAAGACACA	54542
rs529774686	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122870090	CCTCAAAAAATAAAA[A/C]TTGGCCGGGCATGGT	54542
rs529953415	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880377	TGAGACTTTGTAAGC[C/G]TCACTGCTTTTATGC	54542
rs530057835	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851662	CCGCCACGCCTGACT[A/G]GTTTTCGTATTTTTT	54542
rs530059053	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867217	CCCGGCAGCCACCCC[A/G]TCCGGGAGGGAGGTG	54542
rs530096138	snp	A/G	0.000399281	0.0141238	synonymous-codon	RC3H2	GRCh38.p7	9:122858744	TCCATCTAATGAGTT[A/G]TATCTTTCCCGCAAA	54542
rs530163205	snp	A/C	1.6577e-05	0.00287893	intron-variant	RC3H2	GRCh38.p7	9:122851275	TGAAAGTATTTTATA[A/C]ATTTTCAATCAAACA	54542
rs530164021	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902271	TAATATTAGTGATGA[C/T]GAGAAAAATACTTTC	54542
rs530201805	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901688	CCTCCGCCTCCCGGT[C/T]TCATACGATTCTCCT	54542
rs530219438	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122898643	AATTCCAGCTACTAG[C/G]GAGGCTGAGGCAGGA	54542
rs530262056	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865823	TCAAATTCTACTGCA[A/G]CAGATGCCACATGAA	54542
rs530262705	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889135	TGTGTATGTTTGTTA[C/T]GTAATTTATAAATAT	54542
rs530355559	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881270	GGTGGGCAGATCACT[G/T]GAAGTCAGGAGTTTG	54542
rs530437380	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895848	AACCTATGGTAAGAA[C/T]TAGTAATAATAAATG	54542
rs530455719	snp	G/T	0.00557542	0.0525036	intron-variant	RC3H2	GRCh38.p7	9:122852059	GAAGTGAGGAGCGCC[G/T]CTTCCCGGCCGCCAT	54542
rs530457299	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122887997	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	54542
rs530514786	snp	A/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122873120	GAAAGAAAATATAGG[A/T]AAAATTAATTTATTT	54542
rs530535950	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887184	AAATTGTGATTTTTC[C/T]AATTGTATCATTTTC	54542
rs530583573	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122862943	TATTTTGTTAAAAAA[C/T]TGAGATACAGTTCAT	54542
rs530600778	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884020	AAAAATTAGGCCGGG[C/T]GCGGTGGCTCACGTC	54542
rs530639247	snp	A/G	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122895388	GTCCAGGCTAGTCTC[A/G]AACTCCTGGCCTCAA	54542
rs530711292	snp	C/T	0.000331257	0.0128654	missense	RC3H2	GRCh38.p7	9:122858958	GAAGAATTCATTCGA[C/T]CTCGAGGGGAAAATG	54542
rs530711342	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122866737	GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCGC	54542
rs530799977	snp	G/T	0.00874735	0.0655527	intron-variant	RC3H2	GRCh38.p7	9:122865894	ATAGCAAGCCGAGTT[G/T]ATATGTATTTTTTTT	54542
rs530854118	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895935	CAAATCTAGAGTCTT[A/G]CTTTGATTCAATAAA	54542
rs530881956	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889314	ATAAAGAAATATATT[A/C]TTTTATTGGTTTTTA	54542
rs530887246	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896657	TACCTATTACTGAAT[A/G]AAGTTCAATAACTAT	54542
rs531002028	snp	C/G/T	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122875488	TGTGGCTGTTTTTTT[C/G/T]CTACAGTGGCACTGC	54542
rs531072502	snp	A/G	0.00438332	0.0466095	intron-variant	RC3H2	GRCh38.p7	9:122851709	TCGCTGTGATGGCCG[A/G]GCTGGTCTCCAGCTC	54542
rs531174477	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122875426	ATAGTTTCTGTAAAG[C/G]GTTTTTATAAATAAA	54542
rs531245779	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881997	GGGAGGCTGAGGCAG[A/G]AGGATGGCCTACGCC	54542
rs531247940	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889954	CCAGACCAGTCTGGC[C/T]AACATGGTGGAACCC	54542
rs531395229	snp	A/T	1.65633e-05	0.00287774	synonymous-codon	RC3H2	GRCh38.p7	9:122855290	AATCGCACCCCATTT[A/T]GAGATGATGGGTCCA	54542
rs531417484	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907105	TCACTCTGTCACACA[A/G]GCTGGAGTGCAATGG	54542
rs531536517	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RC3H2	GRCh38.p7	9:122849171	AATAAAGCAGCTGGA[A/C]TGAGATGGAAACTTC	54542
rs531570582	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122885680	AGATAAAATTAACCA[C/T]TTTAACCACATAATT	54542
rs531582190	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864406	AAGCAAATATTTACT[C/G]AGTGCTTACTATCTG	54542
rs531640032	in-del	-/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122897122	AAATCACAAAAAAAA[-/T]CTCACAATGTTTTAA	54542
rs531661029	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885029	TCACACTTGAATAAA[C/T]ACTATAAAAGATATT	54542
rs531661049	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892691	GCTGGGATTACAGGG[C/G]TGAGCCACCGCGCCC	54542
rs531668774	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863851	AAGCGATTCTCCTGC[C/G]TCAGCCTTCCCAGGT	54542
rs531826920	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850961	AAAATCCAGATTGAC[A/C]AAATCATTGCCCATA	54542
rs531843915	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871176	TTCCTGTTCCTGACT[A/G]AAGCCAGTCTCACCA	54542
rs531844810	snp	G/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122857795	TATTCAGTGTTTATT[G/T]AACTAAACTCAATTG	54542
rs531963746	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122893549	TTAACAGCAGGAGCT[A/G]TGTGGATTAATGAAG	54542
rs532013635	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901067	TCTCTTATTAGTCCA[C/T]CATATTATGCAGCCA	54542
rs532207410	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849466	TTCATAATGCTAATG[C/T]AAGAGGGCTTGAAGT	54542
rs532212873	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899993	TGTGGGGCTTGGGGT[G/T]GGGGAGTTTCAACCA	54542
rs532259953	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122874561	CTTGCTCTGCTGCCC[A/G]GGTTGGAATACAGTG	54542
rs532349575	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857913	ATTAAGTAATTAAAA[C/T]CTTTCTTACATCCGC	54542
rs532464654	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865074	AGAAAATAAGGTGTG[A/G]AAAAAAAACAATTCT	54542
rs532465610	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878676	AATACATGTAAAACA[C/T]TGAATGTAGTGAATG	54542
rs532513523	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901651	GGCTGGAGTGCGGTG[A/G]TGCGATTTCGGCTCA	54542
rs532528853	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867261	CCCGCCCGGCCAGCC[A/G]CCCCGTCCGGGAGGG	54542
rs532550211	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122888041	TGAGCCACTGCGCCT[A/G]GCCTTGTATCTTTTT	54542
rs532557173	snp	C/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905891	AAAGTGGGGGGGGGA[C/G]GGGGGGAAGAAAGCT	54542
rs532617928	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902032	TCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	54542
rs532627444	snp	C/T	0.0107246	0.0724382	intron-variant	RC3H2	GRCh38.p7	9:122851634	GCAGAGTGCCTGCAA[C/T]TGCAGGCGCGCGCCG	54542
rs532637079	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894781	GCTACTTGGGAGGCT[G/T]AGGCAGGAGAATCAC	54542
rs532642479	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864468	AATTCACTTAATCCT[C/T]GCAACCAACATATGA	54542
rs532780958	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887240	GCTAAAAGAGGAAAC[C/T]TTCCTCAATATATAA	54542
rs532818582	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894191	GTGAACCTGGGAGGC[A/C]GAGCTTGCAGTGAGC	54542
rs532828156	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860847	AAAGAAAACAGACAT[A/G]GTAAGAAAAGAGTTG	54542
rs532886260	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868305	GGAATAGAAAGGGGG[C/G]AAAGGTGGGGAAAAG	54542
rs532902227	in-del	-/GGGGTTTCGCTGT	0.0494519	0.149266	intron-variant	RC3H2	GRCh38.p7	9:122851688	TTTTTTGGTGGAGAC[-/GGGGTTTCGCTGT]GATGGCCGGGCTGGT	54542
rs532998173	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891059	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	54542
rs533011510	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122890608	ATAAAAGTCAATTTT[C/T]ATTATCTGCATTTAA	54542
rs533018043	snp	A/G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887942	TAGAGACAGGGTTTC[A/G/T]CCATGTTGGCCAGGT	54542
rs533049409	snp	C/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122876111	AAGAACTGAGAAATA[C/T]ATAGGAAGATGAATT	54542
rs533104008	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891439	CACTACAATTGATCT[A/G]TTCACTACTTCCAAT	54542
rs533105527	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853802	TAAGAAATCTGGGAT[G/T]ACAATTTTATTTCTG	54542
rs533126461	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122893719	AATTTCAAAATTAAA[A/G]AGTGGAGAAAAAAAG	54542
rs533145433	snp	C/T	1.65776e-05	0.00287898	intron-variant	RC3H2	GRCh38.p7	9:122877603	AAAAATGGGAACACA[C/T]TCAATGAGTGGCAAG	54542
rs533185864	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884834	CTCCAGCCTGGCGAC[A/G]TAGCGAAAGTCCGTC	54542
rs533195737	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898417	AACTGAAAAGGCACA[C/T]AGAAAAAAACAGTGA	54542
rs533224731	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122879661	ACTTATGAGTCACAT[-/A]ACGGAGTCCAATTAA	54542
rs533268514	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884235	GAGGTGGAGCTTGCA[A/G]TGAGCCGAGATCGTG	54542
rs533326737	snp	A/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122899083	AAATTCTATTAGCCT[A/T]TATTGTGTTTTTTTT	54542
rs533351357	snp	C/T	1.71346e-05	0.00292694	intron-variant	RC3H2	GRCh38.p7	9:122883408	AGGAACATGAGTTCA[C/T]GACAAATGAGGAACC	54542
rs533423963	snp	A/T	0.0832709	0.186283	intron-variant	RC3H2	GRCh38.p7	9:122852979	GAGAAATCGGATGGT[A/T]GCCGTGTCTGTGTAG	54542
rs533511107	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883129	TTGCTAGGGCCTCTA[C/G]ACTGGGTAACATGAA	54542
rs533543024	snp	C/G	0.000399281	0.0141238	missense	RC3H2	GRCh38.p7	9:122855395	ATCACCACTGTCCAG[C/G]TCCTATGTAAACCAA	54542
rs533601185	snp	C/G	0.000188395	0.00970371	intron-variant	RC3H2	GRCh38.p7	9:122890230	AAAGACGGGTTGAGT[C/G]TCAGGATTCACCGAG	54542
rs533641388	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863003	TAGTATATTCACAAG[A/G]CTGTCCAATTATCAC	54542
rs533733498	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877095	TTTTGTTGTGAGGCA[C/G]AGTCTTGCTGTGTCC	54542
rs533818321	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122897950	GTTTTGTTGTTTAAA[A/G]AAGTGTTTCCCTTGG	54542
rs533868285	in-del	-/AAAAGG	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122900752	GAGATAAAATGGACT[-/AAAAGG]CCTACAACTCAAGAT	54542
rs533904152	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898780	AGTTCCATAAGTTTA[C/G]TAAAGTAAAAGATTT	54542
rs533962488	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849053	ATGCAGTAAAGAATG[A/C]TAGTATATAACCCTG	54542
rs534036944	snp	C/T	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122869816	CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	54542
rs534041093	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122868613	ACGCTGCGGAAGGCC[A/G]CAGGGTCCTCTGCCT	54542
rs534094677	snp	C/G	0.0178098	0.0926698	intron-variant	RC3H2	GRCh38.p7	9:122861880	TAGGTACAAACGTAA[C/G]GGTTTAGAGTATAAA	54542
rs534118598	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122883738	GTAAATCCCAGCACG[C/T]TGAGAGGCCGAGGCA	54542
rs534179576	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854894	GGATCACATGAGGCC[A/G]GGAGTTCCAGACCAG	54542
rs534268046	snp	C/T	3.31994e-05	0.00407414	missense	RC3H2	GRCh38.p7	9:122855800	CATTTATACAGGAGC[C/T]TATGGTGCCACAAGA	54542
rs534292208	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901858	CCTCCCAAAGTCCTG[A/G]GATTACAGGCATGAG	54542
rs534352319	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865294	AAATAAAAACACTCA[C/G]GCATTTCTAAAAAGG	54542
rs534373016	snp	G/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122857607	TAGCTTTATGCAAAT[G/T]TACTAATACAGTGCT	54542
rs534428583	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873171	GAATTTCTGGTGTTA[C/T]GTGAACTAAGACAAA	54542
rs534450171	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892410	GAAGCCACCACACCC[A/T]GCTTGAATTCTTTTT	54542
rs534495083	snp	A/G			utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897560	GATCATTATTTTGCT[A/G]TGTAGTGTTTTGTAA	54542
rs534561898	snp	A/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122895304	TCCCAAGTAGGTGGG[A/T]CTACAGTCACACACC	54542
rs534591860	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122902516	GAGCCATTATAATCC[A/G]AGTAATTTTTAATTT	54542
rs534599152	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122860195	CTGTCCTCCTTACTA[C/G]AAATTTTTAATAAAA	54542
rs534823261	snp	A/G	3.3227e-05	0.00407583	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879907	GGCATGGGGGTTGGG[A/G]GGGAAGAATGTTAGC	54542
rs534859830	in-del	-/AG	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122877094	GTTTTGTTGTGAGGC[-/AG]AGTCTTGCTGTGTCC	54542
rs534885853	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851804	TCACTCAGTGCTCAA[C/T]GGCGCCCAGGCTGGA	54542
rs534905415	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894478	CAAGAGGTGAAATTA[C/T]AGAGCAAAGATAAGG	54542
rs534922578	snp	A/G	3.43342e-05	0.00414318	missense	RC3H2	GRCh38.p7	9:122859049	TGGACCTCACAAAGC[A/G]AGGAACACAGGGAGC	54542
rs534923476	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851580	TGCTGCCATCTCGGC[C/T]CACTGCAACCTCCCT	54542
rs534975727	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860349	CTGTGTGGGCCACAG[A/G]GAATAAAAACGATTC	54542
rs535013631	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122867429	GTCAGCACCCCGCCC[A/G]GCCAGCCACCCCGTC	54542
rs535126339	in-del	-/T	0.00398564	0.0444627	intron-variant	RC3H2	GRCh38.p7	9:122888490	GGTATTAGTCTTCTA[-/T]TTTTTTTGCCATTGT	54542
rs535141116	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889416	AATGCATCTAATTTT[A/G]CTTTTTCCGCATTTT	54542
rs535185656	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122866482	CTGTACTGCTGCCAT[C/T]TCGGCTCACTGCAAC	54542
rs535202613	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904929	GCCCTACCAGAGAGA[G/T]GGGCCTCCGCAGGGC	54542
rs535214141	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860915	CCTTGAGGAAAGGCC[A/T]CTTTTGTTTATTTTG	54542
rs535240519	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904130	GATTACTTAAAGCAC[C/T]TTATTTGGGATACAA	54542
rs535256042	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882186	TAAGTAGTAAAAAAA[A/T]CTACACATTCAAAAG	54542
rs535342197	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122888626	CTTACCAACGTATCT[A/G]GAGGTCACACCCTAG	54542
rs535399724	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903908	AAAGGTTTTTTAAAA[A/G]GGAGAATCTATTAAT	54542
rs535514257	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122885209	GTATTAAAAGGAAAG[A/G]AGCATAAAACAAGCA	54542
rs535547487	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122858238	TCTATTCTCCATACA[C/G]TTAAAATAAAAAGGT	54542
rs535781608	snp	A/G	0.0310518	0.120672	intron-variant	RC3H2	GRCh38.p7	9:122852386	CTCCGCCCGGCAGCC[A/G]CCCCGTCCGGGAGGG	54542
rs535850721	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868449	GACCTTACCCCCAAC[C/G]CTGTGCTCTCTGAAA	54542
rs535900195	snp	G/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122878808	GGCTGGAGTGCAGTG[G/T]CGCGATCTCGGCTCA	54542
rs535967536	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882833	AATGAGATAACAAAC[A/G]TAATAATGGGTTACA	54542
rs535984268	snp	C/G	0.0150606	0.0854603	intron-variant	RC3H2	GRCh38.p7	9:122899223	TTCTCCCGCCTTGGC[C/G]TCCCAAGTAACTGGG	54542
rs535988059	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122885990	CCTCCTAGGTTCAAA[C/T]GATTCTTGTGCCTCA	54542
rs536029076	in-del	-/A	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122856709	GAATAAGGAATACTT[-/A]ATAGGACCAGAATAC	54542
rs536036001	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122899214	TTCAAGTGATTCTCC[C/T]GCCTTGGCCTCCCAA	54542
rs536052136	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905629	GGCTTCCTAGACGCT[C/G]GTTTGAGCGAGTGTC	54542
rs536129338	snp	A/G	0.0119091	0.0762411	intron-variant	RC3H2	GRCh38.p7	9:122861500	CGTCTCAAAAAAAAA[A/G]AAAAAAAAAGAAAAG	54542
rs536166076	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869292	TAATTATATATGCCT[A/C]AAGTAATGTTATTAA	54542
rs536249788	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871381	CAGCTCACTGCAAGC[A/T]CCACCTCCCAGGTTC	54542
rs536287907	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122859313	ATGCCCAGGCTGGTC[A/G]CAAACTCCTGGGCTC	54542
rs536376934	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878070	CTATTTGAGTTCATA[C/T]AATGAGGCAGAATAT	54542
rs536387625	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850565	CTCCTGCCTCAGCCT[C/G]CCAGGCAGCTGAGAA	54542
rs536420687	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901174	CATTTTACAATTCTC[C/T]TAATAAAAATGTAAA	54542
rs536420929	in-del	-/T			utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849521	GCCCCCAGTAATATC[-/T]TTTTTTTTAAAAAAA	54542
rs536446038	snp	C/T	9.93608e-05	0.00704773	missense	RC3H2	GRCh38.p7	9:122865457	GTACTGTCAGTACTA[C/T]GTGAGATTAGCTGGG	54542
rs536478090	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122900254	GTAAAACACTGCCAA[A/G]ATTTTGGCAATAACT	54542
rs536522761	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864617	GTGTGGCTCCAAAGA[G/T]TCCCCTCCTTTTTTT	54542
rs536556118	snp	C/G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894025	CGCACTTTGGGAGGC[C/G/T]GAGGCAGGCGGATCA	54542
rs536568119	snp	A/T	1.94233e-05	0.00311629	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880844	CTGTGCTTTCTCCCT[A/T]CAACTGATTCGTTTA	54542
rs536608406	snp	A/G	1.65855e-05	0.00287967	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880037	TCTAAATGAGGCCTC[A/G]GTCTATTTAAGTTAG	54542
rs536674758	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872382	AATATAGAAGTTTAA[A/C]TTGTCTCCATCCATG	54542
rs536688537	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894254	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA	54542
rs536760647	snp	A/G	3.48032e-05	0.00417138	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879741	GCAGTCAGAAATGTA[A/G]TAAATGTACTTACCT	54542
rs536766613	in-del	-/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122860829	AGTGGAACTATTTGA[-/G]ACAAAGAAAACAGAC	54542
rs536809919	snp	A/G	0.00438332	0.0466095	intron-variant	RC3H2	GRCh38.p7	9:122894397	CTTTGTGGAGCTCAC[A/G]TTCTAGTGGAGAGGA	54542
rs536826807	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122863738	AGGGAAGATTGTAAA[A/C]GTCCTTTTTTTTTTT	54542
rs536840686	snp	C/T	1.65685e-05	0.00287819	synonymous-codon	RC3H2	GRCh38.p7	9:122851365	TTCATCAGTATCAAG[C/T]GCTGAAAGCTCTAAC	54542
rs536855245	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901727	CTCCTGAGTAGCTGG[A/G]ATTACAAGTGCGCAC	54542
rs536902831	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122873437	AAGAACCCTTGCCAG[A/G]TGCCATGGCTCATGC	54542
rs537032627	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122864672	GTTGCCCAGGCTGGA[C/T]TGCAGTAGCACGATC	54542
rs537162702	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122871459	CCCACCACCAGGCCC[A/G]GCTAATTTTTTCTGT	54542
rs537236821	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122859211	AATATAATAAGCTTT[C/G]AACCTTACCTTACCC	54542
rs537273653	snp	A/G	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122866529	CCTGCCTCAGCCTGC[A/G]GAGTGCCTGCGATTG	54542
rs537342238	in-del	-/CAAACAAA			intron-variant	RC3H2	GRCh38.p7	9:122870409	AAACAAACAAACAAA[-/CAAACAAA]AAAAAAACAACAAAC	54542
rs537344380	snp	A/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122865229	AGTGTTTCTTCTACA[A/T]CACAAAATATTCTGC	54542
rs537344464	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857592	GAGAATTAAATAAAA[C/T]AGCTTTATGCAAATG	54542
rs537357928	snp	A/G	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122874046	ATGGTGAAGGATGCA[A/G]TTAACACTGCCTAGG	54542
rs537393642	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881397	CGGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGATA	54542
rs537394874	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122876542	CTGAGGCAGGAGTAT[C/T]GTTTGAACAGGGGAG	54542
rs537480379	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880849	CTTTCTCCCTTCAAC[A/T]GATTCGTTTATTCCT	54542
rs537485534	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883768	AGGACGACTGTTTGA[G/T]CCCAGGAGTTTGAGA	54542
rs537486974	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888205	ATTTAGGATTTATTA[A/T]ATATTCCACTAGGGA	54542
rs537533115	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894921	AGACAGACTGAACGT[C/T]CTAGGCAAAGGTAAC	54542
rs537624926	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122893691	TTTTGCAACTTTTTT[G/T]TAAGTCTGAAAGAAT	54542
rs537632879	snp	G/T	0.000264975	0.0115073	synonymous-codon	RC3H2	GRCh38.p7	9:122857992	TGCCACAGGAAGAGT[G/T]GAAGAGACAAGAGGT	54542
rs537642821	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122867136	GCCCGGCAACCGCCC[C/T]GTCTGAGAAGTGAGG	54542
rs537686437	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891391	CTCGCTATTTCCTAG[C/T]CTAGTGCCTTAACTA	54542
rs537760389	snp	A/C/T			intron-variant	RC3H2	GRCh38.p7	9:122863794	CAGGCTGGCGTACAA[A/C/T]GGTGCGATCTTGGCT	54542
rs537802716	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884458	CCTCTGAATGCAAAA[A/C]CCAAAGAAGGTATTA	54542
rs537816475	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892527	CGCCATTCTCCTGCC[A/T]CAGCCTCCGGAATAG	54542
rs537816490	snp	C/T	0.0138799	0.0821421	intron-variant	RC3H2	GRCh38.p7	9:122893768	CCCCAAAGCACTTAT[C/T]ACCTTTTTACTATAT	54542
rs537830227	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122868342	AAATCGGATGGTTGC[C/T]GTGTCTGTGTGGAAA	54542
rs537948280	in-del	-/CCT	0.0012053	0.0245194	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905290	GCCGCGACGGGGCCT[-/CCT]CCTCCTCCTCCCTCC	54542
rs537961175	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863167	TGGACATTTAACATA[A/T]ATGTGACCTTTTGTA	54542
rs537981850	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906778	ATCGAAGACGTTTCT[C/T]CCACACATTATCTTT	54542
rs538004544	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886550	CATTGGTTATGTTCC[A/G]TTTTAAAAATTATGG	54542
rs538022683	in-del	-/T			intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880206	CAATTTATCAACATA[-/T]TTTAATACGTTTTCA	54542
rs538092939	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886061	CCCAGCTAATTTTTT[C/T]CTATTTTCAGTAGAG	54542
rs538129942	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893134	TAAAATTATCATGCA[C/T]AGATAATACATGAAA	54542
rs538157232	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877117	GCTGTGTCCCTCAGG[C/G]TGGAGTGCAGTGGTG	54542
rs538170801	in-del	-/AA			intron-variant	RC3H2	GRCh38.p7	9:122896122	ATAGCTGATGAGTTA[-/AA]AAAAAAAAAAAAAAA	54542
rs538194865	snp	C/T	0.000131107	0.00809546	intron-variant	RC3H2	GRCh38.p7	9:122849854	GACATTAAAAACAAA[C/T]TAGCTTTAAGTGCAA	54542
rs538242111	snp	C/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122899468	CTTGCTATGTAAAAA[C/G]CACCCCTATACAAAC	54542
rs538295672	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122890159	CAAAACAAAACAGCA[A/G]TAACAACAACAACAA	54542
rs538311494	snp	A/T	5.01048e-05	0.00500499	missense	RC3H2	GRCh38.p7	9:122855843	ATGGGAAAGATGATC[A/T]TCTTCAAATTTTGTA	54542
rs538343075	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122868123	GGAGGGAGGTGGGGG[-/T]GTCAGCCCCCCGCCC	54542
rs538358690	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885870	CATTTAACGTGTTTT[C/T]TGTTTTGTTTTGTTT	54542
rs538488436	snp	G/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122871296	ACCTGCTCAAATGTT[G/T]TATCTTCTTTTTTTT	54542
rs538592109	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877937	TAAAAAGCATTAAAA[A/G]AAAACCAAAAGCTTT	54542
rs538607864	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886180	CAGGTGTGAGCCACC[A/G]TGCCCAACCTAACGT	54542
rs538617234	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893887	GAATGACCTTGAGTA[A/C]ATTACTTAACTGCTC	54542
rs538636371	in-del	-/CTGGGAGGCTGA	0.00993419	0.0697739	intron-variant	RC3H2	GRCh38.p7	9:122896779	TGTAGTCCTAGCACC[-/CTGGGAGGCTGA]GGTGGGCGGATCACC	54542
rs538677092	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885090	ACTACAAATTGTATA[C/T]AGTACTGTATTGTAT	54542
rs538679355	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877230	GTGGGCCACACAGCT[A/G]ATTTTTAAATTTTTT	54542
rs538689541	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122864320	AACCTTTTTCTAAAG[A/G]CACCAAAACCCTCTG	54542
rs538719116	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122849930	TTTAGGAGTCTCTAG[C/T]AAAGACATGTCTTTA	54542
rs538802087	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872516	TCTTTGCTATGGCCA[A/G]AATTGCTTATTTACA	54542
rs538817257	in-del	-/TA	0.0535932	0.154675	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906924	TTCCACCCTACTGTG[-/TA]TATATATATATATAC	54542
rs538877928	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904411	CCTGAAAGCTAAGGA[C/T]AGAAAAAAGTACAGC	54542
rs538888056	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879927	AGAATGTTAGCAGTA[A/G]TTCTCTTGTGTTATT	54542
rs538941119	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886622	TGAAGCCAGAAGTTC[C/T]GAAGTTACAGTGGGC	54542
rs538942515	snp	A/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122870569	ATATACACTGAATTC[A/T]TAGTATTGGGGCAGC	54542
rs538970313	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122900520	AGAAAATATTTTTGT[A/T]ACTACCAAAAATGGT	54542
rs538979867	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122864018	TTGGGATTACAGGCC[C/T]GAGCCACCGTGCCCA	54542
rs539033758	snp	G/T	0.0174175	0.0916809	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853295	AGACCTTTGTTCACT[G/T]GTTTATCTGCTGACC	54542
rs539063346	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896294	ATATACATCCCTACA[C/T]AGACCTTATTGTTTC	54542
rs539071260	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893245	ATGCCCGTAATCCCA[A/G]CACTTTGGGAGGCCA	54542
rs539084839	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901095	CCAGTTCAGGTCTAC[A/G]GCATCTGATTTTAAA	54542
rs539128229	in-del	-/T	0.287346	0.247195	intron-variant	RC3H2	GRCh38.p7	9:122878923	TGGCTCATTTTTGTA[-/T]TTTTTTTTTTTTTAG	54542
rs539213604	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875964	GTAAATCTGTGCTTT[C/T]AAAATATTTCTGTTT	54542
rs539290988	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882919	TGTAAAGAAATGAGG[C/T]TTCTGCAGTCCACTT	54542
rs539332821	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122898869	AATTCAAGACTTAAC[A/G]TAAGTCTGACAAAAG	54542
rs539381998	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896980	GCAGTGAGCCCAGAT[C/G]ACGCCACTGCACACC	54542
rs539422142	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904746	GCTGAAAAGCTAGGA[A/G]AAGACTTGGTTTCGA	54542
rs539566741	snp	A/G	0.0138799	0.0821421	intron-variant	RC3H2	GRCh38.p7	9:122868557	AGCATGCTCGTTAAG[A/G]GTCATCACCACTCCC	54542
rs539732351	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906458	ATCACTTGAACCCGG[A/G]AGACGGAGGTTGCAG	54542
rs539804897	snp	C/T	0.00132509	0.0257058	intron-variant	RC3H2	GRCh38.p7	9:122875242	TGTTTCTGCTCTTTT[C/T]ACTGCACACACACTT	54542
rs539824164	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122877131	GCTGGAGTGCAGTGG[A/T]GTGAACACACTCACT	54542
rs539937904	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876102	AGAAGAATAAAGAAC[C/T]GAGAAATATATAGGA	54542
rs540070563	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868715	CAAATCCCCCTCTGT[A/G]AGAAACACCCAAGAA	54542
rs540087697	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860698	GCATTACAGGCATCA[A/G]CCACCGTGCCTGGCC	54542
rs540103783	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854823	AAGCACAGTGCTTAG[C/G]ACAGGCACAGTGGCT	54542
rs540156199	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876035	TAAGACTAGTGAGAA[A/G]GCAACAAGGGATCGA	54542
rs540160146	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868238	CACCCCGTCTGGGAG[A/G]TGTACCCAACAGCTC	54542
rs540263006	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122874195	AAAGAAATTTATATA[A/G]TAATCAACAGTGATT	54542
rs540275696	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890890	CTCTCCCACATTATC[A/G]AATTTTCCCTCTTTA	54542
rs540324646	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905872	GTTTCTAGACAAAGA[A/G]TCCAAAGTGGGGGGG	54542
rs540420085	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861234	GGTGGCTCACACCTG[C/T]AATCCTAGCACTTTG	54542
rs540514948	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884676	TGGCCAACATGGTGA[A/G]ACCCCATCTCTATTA	54542
rs540636718	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901315	CTTAAAAATAATTAG[A/T]TTTGTTCTTAAAAAA	54542
rs540723659	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900945	TTTCCAGACTGTAAG[C/T]TCCTTGCTATGAGTG	54542
rs540724781	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853706	GCAGTGAGCCAAGAT[C/T]GTGCCATTGCACTCC	54542
rs540791891	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869619	CCAGGCTGGAGTGCA[A/G]TAGTGTGATCTCAGC	54542
rs540962613	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122860558	AGATGGGACTACAAG[G/T]GCATGCCACCACACT	54542
rs541096245	snp	A/G	0.00478085	0.0486577	intron-variant	RC3H2	GRCh38.p7	9:122850190	ATGTTGGCCAGGCTG[A/G]TCTAGAACTCCTGAC	54542
rs541101301	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865767	GAGGAAACAGTTTTG[A/G]CAAAAAGTTTCTTCA	54542
rs541134908	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856991	CTAAGTTTGACAAGA[C/T]CTATTTGGATCTAGT	54542
rs541184299	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872927	CGCTTTTGACACTCC[A/C]CAGAATGTAGCAATT	54542
rs541184419	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880979	CAGAACTTACATAAC[G/T]AAATACATAATCCTT	54542
rs541194350	in-del	-/AG	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880473	TAAGGATAATTTATA[-/AG]AGTCTGACATTTAAA	54542
rs541236309	snp	G/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122889048	GCATCTTTTGTCAAT[G/T]TTTCAGTTGGTTGTT	54542
rs541269021	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122887867	TCGTGCCTCAGCTTC[A/G]CGAGTAGCTGAGATT	54542
rs541293302	snp	C/G	0.0154538	0.0865337	intron-variant	RC3H2	GRCh38.p7	9:122851936	CGTCTGGGAAGTGAG[C/G]AGCGTCTCTGCCTGG	54542
rs541410939	snp	A/C	0.0236746	0.106192	intron-variant	RC3H2	GRCh38.p7	9:122866559	GCAGGCGCGCGCCGC[A/C]ACGCCTGACTGGTTT	54542
rs541427720	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887945	AGACAGGGTTTCGCC[A/G]TGTTGGCCAGGTTAG	54542
rs541428846	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894607	GAGAGAGGCTGGGCA[C/T]GGTTGCTCACGCCTA	54542
rs541472122	snp	C/T	0.0107246	0.0724382	intron-variant	RC3H2	GRCh38.p7	9:122851837	GCAGTGGCGTGATCT[C/T]GGCTCGCTACAACCT	54542
rs541514947	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894109	CTAAAAATACAAAAA[A/G]TTAGCCGGGCGTGGT	54542
rs541650909	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895730	TTATTGGATTTTCTA[C/T]TAAATCAGAAAAATA	54542
rs541778323	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122902251	TCTATTTTAACAAGT[A/G]TAACTAATATTAGTG	54542
rs541846313	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852094	TCTAGGAAGTGAGGA[A/G]CGTCTCTGCCCGGCC	54542
rs541873956	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122851614	TGATTCTCCTGCCTC[A/G]GCCTGCAGAGTGCCT	54542
rs541875023	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903660	GTTTGAATTATAACA[A/T]CTGCTTTTTCTAAAC	54542
rs541997129	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122865866	ATTCACATATAATAT[A/C]CATGTAATTAATATA	54542
rs542047888	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881716	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTAGGC	54542
rs542055297	snp	C/T	0.00795532	0.062565	intron-variant	RC3H2	GRCh38.p7	9:122879126	TTCGGCCAGGCACGA[C/T]GGCTCACGCCTGTAA	54542
rs542085019	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873565	AATATAAAAAAAATT[C/T]AGCCAGGCATGGTGG	54542
rs542314876	snp	A/C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122849938	TCTCTAGCAAAGACA[A/C/T]GTCTTTATCACTAGA	54542
rs542366656	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122866654	GCGAGTGATCCGCCA[A/G]CCTCGGCCTCCGGAG	54542
rs542446483	snp	A/G	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122889917	GAGGCTGGGGCAGGC[A/G]GATCACCTGAGGTCA	54542
rs542451233	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862402	CTTCTCTCACACCTT[A/G]TTCATTTTGCCTGTG	54542
rs542510741	snp	C/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122852664	CCCGGCCAGCCGCCC[C/T]GTCCGGGAGGTGAGG	54542
rs542558553	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895244	GGCTCTCTGCAGCCT[C/T]GACCTCCTGGGCTCA	54542
rs542573516	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871566	CTGACCTTGTGATCC[A/G]CCTGCCTCGGCCTCC	54542
rs542589870	in-del	-/T	0.15698	0.23205	intron-variant	RC3H2	GRCh38.p7	9:122901929	TGAGATAACTACTTC[-/T]TTTTTTTTTTTTTTT	54542
rs542605390	snp	G/T	0.000807387	0.0200759	intron-variant	RC3H2	GRCh38.p7	9:122855135	AAAAAAAAAAAAAAA[G/T]GCATAGTGCTTAGAA	54542
rs542625905	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906937	GTGTATATATATATA[C/T]ACACACATATATACA	54542
rs542689364	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122865153	GTCACTTTCCCACTT[G/T]CCAAGTTCACAGGGC	54542
rs542702068	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122879213	CCAGCCTGGCCAACA[C/T]GGTAAAACCCTCTCT	54542
rs542767993	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870172	CTGAGGTCAGGAGTT[C/G]AAGACCAGCCTGGCC	54542
rs542779060	snp	C/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122885613	TTCTTTAAATTTTTT[C/T]TTTTTTTGCCTCCCA	54542
rs542814778	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122893353	ACAAAAATTAGCCAG[A/G]TGTGGTGGTGGATGC	54542
rs542850122	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864796	CGGCTAATTTTTTTT[G/T]TGTATTTTTAGTAGA	54542
rs542851230	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857788	GCATTTATATTCAGT[A/G]TTTATTGAACTAAAC	54542
rs542938156	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864358	AAATCTTATGCTGAC[A/C]CTCAGTAACAATTAA	54542
rs542981502	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122891767	CATACACAACAGTGC[-/A]AAGCATTCAACAGGT	54542
rs543082661	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890074	TTGAGCATGGATGTC[A/G]AGGCTGCAGTGAGCC	54542
rs543183269	in-del	-/A	0.00136793	0.0261169	intron-variant	RC3H2	GRCh38.p7	9:122849845	AAAAGAAATGACATT[-/A]AAAACAAATTAGCTT	54542
rs543363998	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850081	TCCTGGATTCAAGCA[A/G]TTCTCCTGCCTCAGC	54542
rs543366790	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864902	GTGCTGGGATTACAG[C/G]TGTGAACCACTGCAC	54542
rs543380371	snp	C/T	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122900775	TACAACTCAAGATAC[C/T]TAAAGTGATTCCTTA	54542
rs543404412	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	RC3H2	GRCh38.p7	9:122849250	TCACTAGATGTATCA[C/T]TGTAGGATCCTGCTA	54542
rs543418819	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899813	GATTAAATATTTATG[A/G]AAACAGGACACTGCG	54542
rs543430683	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856827	TCGAACTCAGCAGAT[C/T]GGAGTCTCAGGGAAA	54542
rs543533221	snp	C/T	9.94678e-05	0.00705153	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880148	ACAGAAATGAGAATG[C/T]TTTTTACTTTGGTTC	54542
rs543604336	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894020	AATCCCGCACTTTGG[C/G]AGGCCGAGGCAGGCG	54542
rs543643687	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886241	TGTATCAGTATTTAT[C/T]CCTTTTATGGCTGAG	54542
rs543651448	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122851631	CCTGCAGAGTGCCTG[C/T]AATTGCAGGCGCGCG	54542
rs543667790	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902112	TTTTTTGTAATTTTA[A/G]TAGAGATGGGGTTTA	54542
rs543702822	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122855422	CCAAAGAAAATCAAT[A/G]AAAGGACTGTTGGCA	54542
rs543728623	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893490	CAGAGTGAGACTCCA[A/T]CTCAAAATAACAACA	54542
rs543751788	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873345	AGAAGTAAGAACTGT[A/G]TATTATTTGCTCCTC	54542
rs543766915	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892702	AGGGGTGAGCCACCG[C/T]GCCCGGCTCTAGCTT	54542
rs543892579	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892661	TGTGATCCGCCCGCG[C/T]TGGCCTCCCAAAGTG	54542
rs544104528	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853331	TCCACTATTGTCCTA[C/T]GACCCTGCCAAATCC	54542
rs544113284	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869399	GTCCTCTGGTATCTA[C/T]AAACAACTTCATTAT	54542
rs544113343	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861289	TGAGGTTGGGAGTTC[A/G]CGACCAGCCTGACCA	54542
rs544113942	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853714	CCAAGATCGTGCCAT[C/T]GCACTCCAGGCGATA	54542
rs544130214	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905312	CCTCCCTCCACCTCC[G/T]CCTCCTCCTCCTCCT	54542
rs544135009	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122889336	TGGTTTTTATTACCA[A/G]TATATTTTTATTTTT	54542
rs544202473	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905285	GCGAAGGCCGCGACG[A/G]GGCCTCCTCCTCCTC	54542
rs544204845	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891902	TTTATTACACTTGTA[C/T]ATCTATCTCCCCCAG	54542
rs544235038	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876083	TTGGATCACAAGGAT[A/G]GAAAGAAGAATAAAG	54542
rs544245683	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122864457	ACTGGAGTATTAATT[C/T]ACTTAATCCTCGCAA	54542
rs544371904	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898814	AGCAAAACGATACTA[A/C]TTTGAACACACTAAA	54542
rs544411576	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905993	TTGAAGCTTTTTACA[C/G]AGCGAACTAAGGTAA	54542
rs544430937	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870952	TAAATAATTCATTAA[C/T]ACGCTTCTTTACTAA	54542
rs544483855	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122885298	GAAAGTGCTGAATGT[C/T]GGTAAAGAATATATA	54542
rs544518746	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878260	ACTGACAGCACAACC[A/T]TTTTTATTTTTTATT	54542
rs544528217	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122873929	TTCAAGCCATTCTCC[C/T]GCCTCAGCCTCCCGA	54542
rs544544864	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122867173	TCCGCCCGGCAGCCG[C/G]CCCATCTGAGAAGTG	54542
rs544719771	snp	A/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122898317	ATTTAGCGATTGATA[A/T]ATATAACCAAAAACT	54542
rs544829615	snp	C/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122870291	GAAGCAGGAGAATTG[C/G]TTGAGCCTGGGAGAC	54542
rs544846743	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881992	TTCTAGGGAGGCTGA[A/G]GCAGGAGGATGGCCT	54542
rs544851150	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899512	TCTAATGCAAATTAT[C/T]TAATATCGTTATCTT	54542
rs544910897	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876439	TTGAGACCCGCCTGG[C/T]GAACATGGTGAAACC	54542
rs544974258	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906510	CACTACAGCCAGGCG[A/G]GGGGGCAGTGCCAGA	54542
rs545103923	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122876673	AGCAGAAAGTAGAAA[A/G]GCTGGGATCAATTTT	54542
rs545157596	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892602	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	54542
rs545174335	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892110	ATGCAGTGACTCTGG[C/T]AAATTTTTTTTTTTT	54542
rs545198916	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122898885	TAAGTCTGACAAAAG[C/T]TCTCTGGTGAACAAG	54542
rs545231938	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122869068	CTGCCACCACGCCTG[C/G]TTAACTTTTGTATTT	54542
rs545266284	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864174	GGCATATAACAGATA[C/T]TGATAGACTATTTAT	54542
rs545288861	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122903267	CAGCTAGCTTTATTT[A/T]ACCCATGCTTCCTTT	54542
rs545306752	snp	C/G	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122871510	CACCGTGTTAGTGGG[C/G]GGGGGGGTTTCATCG	54542
rs545321023	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906847	GAGAACTGTTAACAA[C/T]CAATAATTGTTTCAG	54542
rs545325479	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122900200	ACTGAGAAGTTTAAT[A/T]TCTACCACAAATTGA	54542
rs545337373	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878236	AGTGTAGGTTTGATC[C/T]CAGCTCTTACTGACA	54542
rs545365067	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122861624	TTGACAAAGCTTTAG[A/C]TATGTGATGAGTGAA	54542
rs545397265	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888769	TTCCAGATGTTTGCT[A/G]TTACAAATAGTGCTT	54542
rs545504600	snp	A/G	0.00478085	0.0486577	intron-variant	RC3H2	GRCh38.p7	9:122851914	AGCCTCTGCCCGGCC[A/G]CCACCCCGTCTGGGA	54542
rs545524402	in-del	-/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881656	TGTGAAACCACTGAC[-/T]TTTTTTTGCAGGGGT	54542
rs545606629	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122894723	CATCTCTACTAAAAA[C/T]ACAAAAATTATCTGG	54542
rs545672352	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882374	ATTATCAACTACCTG[A/T]TATCTCAAACTAAGT	54542
rs545705944	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871019	ACTTTCAACCACCCC[G/T]CCTACAGCTAGATGA	54542
rs545757810	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874487	TATTTTTGAATGAGT[C/G]ATATTTTATATATTT	54542
rs545804951	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905182	GGCTTGGCGACGGAG[A/G]CGCCTCGTCTCGCCG	54542
rs545865610	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122867147	GCCCCGTCTGAGAAG[G/T]GAGGAGCCCCTCCGC	54542
rs545873685	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895413	CCTCAAGCAGCCTGC[C/T]CACTTCAGCCTCCCA	54542
rs545888321	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896734	TGCCATTAAAGCCAC[A/G]TAAGATGGCTGGGTG	54542
rs545908507	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903008	TTGAAATCTGGTATT[C/T]TACACCTAAAGCACA	54542
rs545936999	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122867671	GGGAGCGCCTTTGCC[C/T]CACCGCCCCGTCTGG	54542
rs546022336	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875134	TATATAGAACTAGTT[C/T]GATTGGGTACAAACA	54542
rs546046010	in-del	-/ACATATAT	0.00318978	0.0398085	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906960	TATATACATATATGC[-/ACATATAT]ACATATATACATACA	54542
rs546055079	in-del	-/G	0.0232847	0.105357	intron-variant	RC3H2	GRCh38.p7	9:122867153	TCTGAGAAGTGAGGA[-/G]CCCCTCCGCCCGGCA	54542
rs546083128	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891349	TCTTTCTTCTCTTAT[A/G]CAGCAAATTTTCTAG	54542
rs546215255	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853666	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGAGAG	54542
rs546253654	snp	A/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122852853	GTGAGGAGCCCCTCT[A/G]CCCAGCCACCACCCC	54542
rs546259024	in-del	-/CCTGTAATCC	0.00835141	0.0640778	intron-variant	RC3H2	GRCh38.p7	9:122902584	GCGTGGTGGCTCACG[-/CCTGTAATCC]CAGCACTTTGGGAGG	54542
rs546275933	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873847	TTTTGAGACGGAATC[G/T]TGCTCTGTCGTCCAC	54542
rs546335779	snp	A/C	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122860534	TCCTCCCACCTCAGC[A/C]TCCCAAGCAGATGGG	54542
rs546378325	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876145	AGAACTTTTTGACTG[A/G]TTAAGCAGAAAAAGC	54542
rs546379205	snp	C/T	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122870353	GTACTCCAGCCTGGC[C/T]GACAGAGCAAGACTC	54542
rs546406517	snp	A/T	0.00755907	0.0610114	intron-variant	RC3H2	GRCh38.p7	9:122896098	ACATAAGATACACTA[A/T]CACTAACAATAGCTG	54542
rs546408724	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122904579	TGCCATTGCTCCTAG[C/T]CACAACCCCTGTGCA	54542
rs546456632	in-del	-/C			intron-variant	RC3H2	GRCh38.p7	9:122860405	CACCATTTACCCATT[-/C]TTTTTTTTTTTTTTT	54542
rs546461391	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890721	CTATAGTAATAAGAA[A/G]CCTAATTTTTAGCTA	54542
rs546536807	snp	A/C	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122866852	AAGTGAGGAGCGTCT[A/C]TGCCTGGCCGCCTAT	54542
rs546644668	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122867220	GGCAGCCACCCCGTC[C/T]GGGAGGGAGGTGGGG	54542
rs546650771	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122883515	TTAGCACAAAGAGGA[C/T]ATCACACGTACATAA	54542
rs546745620	in-del	-/A	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882178	TTCTACTTAAGTAGT[-/A]AAAAAAAACTACACA	54542
rs546807390	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122853004	GTGTAGAAAGAAGTA[A/G]ACATGGGAGACTTTT	54542
rs546989225	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122875614	AATTAATTTTATGTG[A/G]TAAGTGTTTGAAAGA	54542
rs547068182	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890024	GCGTGTGCCTGTAGT[C/T]CCAGCTACTTAGGGG	54542
rs547133550	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861468	GCACTCCAGCCCAGG[C/T]AACAAGAGCGAAACT	54542
rs547233868	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122864603	TGAAAGCCCAGAGAG[C/T]GTGGCTCCAAAGAGT	54542
rs547244170	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853774	ATCCCGATGATCTAG[C/T]TAAAGAATTATTTAA	54542
rs547322498	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122884122	ACATGGTGAAACCCC[A/G]CCTCTACTAAAAATA	54542
rs547379114	snp	A/C	3.31257e-05	0.00406962	missense	RC3H2	GRCh38.p7	9:122851166	GATGCCCATTTTCCA[A/C]TGCCATTCCATTTAG	54542
rs547392137	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878739	GTATAAAGGATTATA[C/T]CTTAACTTCTTTTTA	54542
rs547415965	snp	A/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122850511	AGTGCAGTGTCACGA[A/T]CTTGGCTCACTGTCT	54542
rs547440058	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122879566	ACACCCAAGATACCC[G/T]CTAAACTCTTGGTGT	54542
rs547554114	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904515	CCAAAAAGGAAAAAT[A/G]AGAGAGGGAAAGAAG	54542
rs547697170	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122879393	AGTGAGACTTTGTCT[A/G]AAAAAAAAAGAAAGA	54542
rs547801514	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122875272	TATCTTCTCTCTATC[A/C]CAATGCTGCTGCTTG	54542
rs547807539	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894238	CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC	54542
rs547860091	snp	G/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906662	TTAGAATATGGAAAG[G/T]TTGCTTCTACAGTTT	54542
rs547890567	snp	A/C	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122865083	GGTGTGAAAAAAAAA[A/C]AATTCTGGTCCAGTC	54542
rs547912248	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893752	ACAGTTGTTTTTTTT[C/T]CCCCAAAGCACTTAT	54542
rs547972641	snp	C/T	0.00438332	0.0466095	intron-variant	RC3H2	GRCh38.p7	9:122886461	GTAATTGTTTAACTT[C/T]TTAAGGAACTGACAA	54542
rs548031031	snp	G/T	1.65644e-05	0.00287783	missense	RC3H2	GRCh38.p7	9:122857958	TGAACAGAGGAGAAG[G/T]TGGTGTTGGTGACTG	54542
rs548171139	snp	A/C	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122872337	ATTGCTATAGTCCTA[A/C]CCGAGCTACCAAACT	54542
rs548260874	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883740	AAATCCCAGCACGTT[A/G]AGAGGCCGAGGCAGG	54542
rs548296354	snp	A/G	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122885991	CTCCTAGGTTCAAAC[A/G]ATTCTTGTGCCTCAG	54542
rs548416935	snp	A/G	0.000314739	0.0125407	missense	RC3H2	GRCh38.p7	9:122851327	GTGGCACTTACTTCA[A/G]TTGGTTCACTTTGTC	54542
rs548433487	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122901694	CCTCCCGGTTTCATA[C/T]GATTCTCCTGCCTCA	54542
rs548471991	snp	A/C/T	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122874662	AGCTAAGATGACAGG[A/C/T]GTATGCCACTATGCT	54542
rs548482693	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873093	TGTTTGGTTAGAGGG[G/T]TGTATAATAGAGAAA	54542
rs548535877	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857554	GTAAAATATGGAAAA[C/T]ACCTGCCCCCTAAGG	54542
rs548593934	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881331	ATCTCAAGAAAAAAT[A/G]CAAAAACTAGTCAGG	54542
rs548600775	snp	C/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122851669	GCCTGACTGGTTTTC[C/G]TATTTTTTTGGTGGA	54542
rs548615282	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902281	GATGACGAGAAAAAT[A/T]CTTTCTTTGAGATAG	54542
rs548675904	snp	A/G	6.62471e-05	0.00575492	missense	RC3H2	GRCh38.p7	9:122858755	AGTTATATCTTTCCC[A/G]CAAAGATGTCTGATA	54542
rs548727578	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874620	CCTCCCGAGTTCAAG[C/T]AATCCTCCCACCTCA	54542
rs548730013	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854757	ATTCTGAGTTTCCCA[C/T]GGTTGTTAAATGGAG	54542
rs548868000	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122859583	TTTTTTGGGAGCAGA[C/T]GTTAAAGACCTCTTT	54542
rs548869869	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122877672	AACTTTATAATTACA[C/T]CTTTAATTCTTTTTC	54542
rs548908598	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884935	GAAAGGCAAAGAAAA[G/T]CTGAGGAACAGTTCC	54542
rs548925313	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888157	TTCTAAATAACAAGA[A/C]CAGAATTATGAACAA	54542
rs548928514	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892505	CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT	54542
rs549042501	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870414	AACAAACAAACAAAC[A/C]AAAAAAAAACAACAA	54542
rs549052280	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122897984	ACCAGTACCCCAAAA[C/T]ATAATAAAGTATGGC	54542
rs549076070	snp	C/T	3.31312e-05	0.00406995	synonymous-codon	RC3H2	GRCh38.p7	9:122854054	GGCCAAAGCATTGGC[C/T]TCTCTCTGAAGAAGT	54542
rs549141866	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905572	AGGCAAGCCGAAGGG[A/T]TTGATGGGAAATTCC	54542
rs549149335	snp	A/G			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853393	TAAAAAAAAAAAAAA[A/G]AAAAGAAAAATACTG	54542
rs549181507	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901006	ATCTCTTATATGATT[C/T]AAATTACAAACTGCT	54542
rs549291167	snp	G/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892138	TTTTTTTGAGACAAG[G/T]TCTCACTCCCATTGC	54542
rs549326142	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891567	CCTTATTTTATCTGA[A/C]CTTCCAACAGCATTC	54542
rs549326340	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122888298	CTACCAACTTGTTTT[A/G]GCTTTATTTTTAGGT	54542
rs549337128	snp	G/T	3.336e-05	0.00408398	missense	RC3H2	GRCh38.p7	9:122849769	TTGCTAATAGACACT[G/T]GGAGTGGCTGGCTAA	54542
rs549362916	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889490	AAAATAAATTCTACC[C/T]GAACTGTAGTTCTAA	54542
rs549435970	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122889177	GGTCTTCTTTTTCAT[G/T]TGCTTATAATTTTTT	54542
rs549436697	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856422	TATGCCCAGACAATC[A/T]TTTTGTATTTTTAGT	54542
rs549670119	in-del	-/T	0.488905	0.0736498	intron-variant	RC3H2	GRCh38.p7	9:122868896	GTGTGTGTGTATGTG[-/T]TTTTTTTTTTTTTTT	54542
rs549676047	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871178	CCTGTTCCTGACTAA[A/T]GCCAGTCTCACCACC	54542
rs549713040	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122878586	CCTGACAGCACAATC[C/T]TATGTTATTTAACCT	54542
rs549744090	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857179	ATATTATTCTCTCTA[C/T]ACTTGTATATGTTTG	54542
rs549804579	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864429	ACTATCTGGTAGGCA[C/T]TGTTCAAGGCATACT	54542
rs549804932	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856597	ACATGTGCAAATAAG[G/T]GAATATAACTGATAA	54542
rs549816506	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122892319	GCTTTCGCCTTGTTG[C/T]CCAGGCTGGTCTCAA	54542
rs549855157	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122891635	TATTTGGCTTACTAA[C/T]GTATCCCAGCACTAG	54542
rs549883627	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898694	GCGGAGATTGCAGTG[A/C]GCCGAGATCACGTCA	54542
rs549920370	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122859495	TATTAACAGACGGAT[A/G]GTAAATATCCTTCTA	54542
rs549933682	snp	C/T	1.68414e-05	0.0029018	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879768	ACCTGAGGGGTCTCA[C/T]GGCCTTTTCTACTAT	54542
rs549935399	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887204	GTATCATTTTCTAAA[C/T]GTATTATTAGTTTGA	54542
rs549935472	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906089	ATTTATAAACTACTT[A/G]GTATGTGTCAGGCAG	54542
rs549952791	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870487	AGTTTTAACTATGAA[A/C]CTCTCAAAAAAGAGT	54542
rs549972358	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122886597	GGGAGGCCGAGATGG[A/G]AGGATCACTTGAAGC	54542
rs550089685	snp	G/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122885713	GTGGTATTTACTACA[G/T]TCACAATGTGTACAA	54542
rs550107331	snp	C/T	2.17346e-05	0.00329649	intron-variant	RC3H2	GRCh38.p7	9:122849855	ACATTAAAAACAAAT[C/T]AGCTTTAAGTGCAAA	54542
rs550112939	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860715	CACCGTGCCTGGCCA[C/T]TACTCATTCTTTAAA	54542
rs550126332	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122885040	TAAATACTATAAAAG[A/G]TATTTTTGGAATAGT	54542
rs550172949	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900304	GTGTCAGAGTCTAGC[C/T]TTCTGACAGTAAATT	54542
rs550200902	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868289	ACAATTGCGGTTTTG[C/T]GGAATAGAAAGGGGG	54542
rs550200947	snp	A/G	0.000399281	0.0141238	missense	RC3H2	GRCh38.p7	9:122860051	TGAGGCACAGAATTC[A/G]GCTCTGTTCCAACAT	54542
rs550204406	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893841	TCAAAGGTCAAAACT[A/T]GGGTAAAAATTGCAG	54542
rs550229810	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871643	TTGTATCTTCTAAGA[A/G]TCTTTCCTACACTAT	54542
rs550232464	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122883673	TGATAATGTTAAGGT[-/A]AAAAAAAGTCATTTA	54542
rs550239431	snp	A/G	0.0162398	0.0886349	intron-variant	RC3H2	GRCh38.p7	9:122866980	TCTGCCCGGCCACCC[A/G]TTGTCTGAGATGTGG	54542
rs550245068	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901069	TCTTATTAGTCCACC[A/C]TATTATGCAGCCAGT	54542
rs550267676	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852406	GTCCGGGAGGGAGGT[G/T]GGGGGGTCAGCCCCC	54542
rs550384073	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851017	GCCAAAAATTAATTT[C/T]GCATTTTTTTCTCTT	54542
rs550516772	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122897852	ATGTATTTTTCTCAA[C/T]GACCACATCAAACAA	54542
rs550632249	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122866199	AAATTCTGTATTATA[A/G]TTCTCAGAATAGTTT	54542
rs550669685	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876807	AGGGACATAGAAAAA[A/G]GGGTTAACCATAGGA	54542
rs550693208	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122898482	CTGCTGGGCGTGGTG[G/T]CTCACACCTATAATC	54542
rs550826069	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882860	TACAAAGTTTACATA[C/T]TCCTTATGAAGTTTC	54542
rs550955648	snp	C/G	3.32474e-05	0.00407708	intron-variant, missense	RC3H2	GRCh38.p7	9:122853900	ATAACCAAGATGCAG[C/G]AGCAGAAAACAAATA	54542
rs550960279	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869294	ATTATATATGCCTAA[A/G]GTAATGTTATTAATG	54542
rs550994312	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861422	TTGAACCCAGGAGGC[A/G]GAGGTTGTGGTGAGC	54542
rs551080276	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860860	ATGGTAAGAAAAGAG[C/T]TGTTTTCTATGAGGA	54542
rs551114213	in-del	-/CC	0.00597247	0.0543191	intron-variant	RC3H2	GRCh38.p7	9:122891008	CCCCTACCAAATCTG[-/CC]CCATTTTTTTTTTTT	54542
rs551154580	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895425	TGCCCACTTCAGCCT[C/T]CCAAAGTGCTGAGAT	54542
rs551168058	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883733	TGCCTGTAAATCCCA[A/G]CACGTTGAGAGGCCG	54542
rs551179736	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906417	GCACCTGTAATCCCA[G/T]CTACTCGGGGGGCTG	54542
rs551208357	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122868965	ACAGTGCAATGGCGC[A/G]ATCTCGGCTCACTGC	54542
rs551238437	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122861958	AACAAGGAAAATGAT[C/T]AGGATTTCCTTAAAA	54542
rs551384280	snp	A/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122898435	AAAAAAACAGTGAGA[A/G]AATTTTTCTTATTTC	54542
rs551405912	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877617	ATTCAATGAGTGGCA[A/C]GGTGAAGATTCCATT	54542
rs551416726	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905401	CTCCCCACTTAACGC[A/G]AGATTACGCAAGCCC	54542
rs551444471	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876985	CACAGGTGCTCAGTA[C/T]AAATATGGATTCCAG	54542
rs551453465	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904819	AGAGTGAAGCCGGGC[C/T]TTTGCTTGGGTGGGT	54542
rs551495068	in-del	-/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881456	GAGTGAGACTCCGTC[-/T]CAAAAAAAAAAAAAA	54542
rs551580124	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899197	AACCTCTGCCTCCCA[A/G]GTTCAAGTGATTCTC	54542
rs551616753	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907255	TATTTTTGTAGAGAC[A/G]GGTTTTCACCATGTT	54542
rs551669564	snp	C/T	0.00597247	0.0543191	intron-variant	RC3H2	GRCh38.p7	9:122893953	AAAATCTGTATTTTG[C/T]AGTGCCGCTATAAAA	54542
rs551690260	snp	G/T	0.00874735	0.0655527	intron-variant	RC3H2	GRCh38.p7	9:122897935	CTGGGCGGTTTTTTT[G/T]TTTTGTTGTTTAAAA	54542
rs551711358	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862178	CATGAAATCATGCAA[A/G]CTATCTCAAAAATTG	54542
rs551797110	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122869741	CACCTGGCTAATTTT[C/T]GTATTTTTAGTAGAG	54542
rs551839698	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880462	TAAAAAGAAAATAAG[C/G]ATAATTTATAAGAGT	54542
rs551858805	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122856455	AGATGAAGTTTTGCC[A/G]TATTGCCTAGGCTGG	54542
rs551969124	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122872399	TGTCTCCATCCATGC[A/T]GACACCAGAGTGATA	54542
rs551998966	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856277	TTCTTTTGAGACAGG[G/T]TCTCACTCCCACCGC	54542
rs552110362	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122898936	ATCAAACAACTAATA[A/C]TTTATTTCACAGGAA	54542
rs552117304	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873649	GCCTGGGAGGCAGAA[C/G]TTGCAAGTGAGCCAA	54542
rs552123147	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122877257	TTTTGTAGAGACGGG[A/G]GTCTCCTTATCTTGC	54542
rs552356312	snp	A/G	0.00676609	0.0577691	intron-variant	RC3H2	GRCh38.p7	9:122859540	ACTGGTTTTGGATTA[A/G]TCAGTTATATCATTG	54542
rs552358341	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851732	TCCAGCTCCTAACCA[C/T]GAGTGATCTGCCAGC	54542
rs552427737	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122866022	GATGTTATGTAAAAA[G/T]GACAGGAACTGGCAA	54542
rs552445997	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122902178	TCAGGTGATCCACCC[A/G]CCTCAGCCTTCCAAA	54542
rs552530043	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901971	TTTCGCTCTTGTTGC[A/C]CAGGCTGTAGTGCAA	54542
rs552577630	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889976	GTGGAACCCTGTCTG[C/T]ACAAAAAATAGAAAA	54542
rs552578630	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874687	TATGCTCAGCCAATT[C/T]TGTTTATTTTTTTGT	54542
rs552615349	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889364	TTTAATAAGGATTTC[G/T]GACGTTTGTAATTTA	54542
rs552640319	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895953	TTGATTCAATAAAAT[A/T]ATTACAAACATGAAT	54542
rs552686591	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122859885	AGGAAACAATGTTTC[C/T]TTTTTTCTTAGAATT	54542
rs552725416	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852212	TGGGAGGTGAGGAGC[A/G]TCTCTGCCCGGCCGC	54542
rs552771449	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122871342	TCGCTCTGTTGCCCA[C/G]GCTGGAGTGCAGTGG	54542
rs552783833	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875513	CACTGCTGAGTGGTT[G/T]TAACAGATTCTGTGG	54542
rs552887310	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882747	CTCCTCAACTTTCCA[C/T]TTCCTGGTTGTATCT	54542
rs552892404	snp	G/T	0.00597247	0.0543191	intron-variant	RC3H2	GRCh38.p7	9:122902579	GCTAGGCGTGGTGGC[G/T]CACGCCTGTAATCCC	54542
rs552956386	snp	C/T	0.00676609	0.0577691	intron-variant	RC3H2	GRCh38.p7	9:122851590	TCGGCTCACTGCAAC[C/T]TCCCTGCCTGATTCT	54542
rs552981605	snp	A/G	0.000234086	0.0108161	intron-variant	RC3H2	GRCh38.p7	9:122858113	TGGGGGATAAAAGAA[A/G]CAATCTTAATCATCT	54542
rs553087923	snp	A/T	0.0429648	0.14013	intron-variant	RC3H2	GRCh38.p7	9:122868745	ATGATCAATAAAAAA[A/T]AAATAAATAAATAAA	54542
rs553111231	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122891980	CTCAATAAAATTTAA[A/T]GAATGACTGAATGAA	54542
rs553149307	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888336	TGATCATTTTTAATT[A/G]AATTTAAAAAATATT	54542
rs553149354	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899394	CGCGCCCGGCCCTGC[A/G]CTTTTATATTCACAA	54542
rs553182808	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882123	GAAGAAATGTTCTGC[C/T]ACCAGAGAAATTATC	54542
rs553242280	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853470	AAAATCCCAATGATC[A/G]GCCAGGCACGGGGGC	54542
rs553318499	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851816	CAATGGCGCCCAGGC[C/T]GGAGTGCAGTGGCGT	54542
rs553340381	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860959	CCCCAGCACCTAAAA[C/G]AGCTCCTGGAACAGA	54542
rs553367021	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122867469	GGTGGGGGGGTCAGC[C/T]CCCCGCCCGGCCAGC	54542
rs553403932	snp	A/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122866562	GGCGCGCGCCGCCAC[A/G]CCTGACTGGTTTTCT	54542
rs553405693	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874914	GAATGTGAAGTCTGT[C/T]TGAAGGTATGAGAAA	54542
rs553447159	in-del	-/GAGGCC			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881247	ATCCCAGCACTTTGA[-/GAGGCC]GAGGTGGGCAGATCA	54542
rs553463617	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870575	ACTGAATTCTTAGTA[C/T]TGGGGCAGCTAAAGG	54542
rs553503265	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RC3H2	GRCh38.p7	9:122849041	CTCCTACATATAATG[C/T]AGTAAAGAATGCTAG	54542
rs553509773	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856659	AAAGGAGGCTCTGGA[A/G]ATAAAGGGGAAATGA	54542
rs553569724	snp	G/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906772	GGCCACATCGAAGAC[G/T]TTTCTTCCACACATT	54542
rs553580671	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852649	GGGGTCAGCTCCCAA[A/C]CCGGCCAGCCGCCCT	54542
rs553583699	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122905003	CCTCGAGGCACCAGG[A/G]GCGACAGCGCACAGG	54542
rs553631646	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122863887	GGATTACAGGCATGC[A/G]CCACCATGCCTGGCT	54542
rs553668331	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904242	AAGGGAACCCAAGGG[C/T]TATGAAAATATAAAT	54542
rs553694878	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122861348	ATACAAAATTAGCCG[C/G]GTGTGGTGGTCCATG	54542
rs553767149	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122863444	AAGACTGGTCTCCTC[A/C]ATATTCCATATAATT	54542
rs553813736	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877981	TTCTCAGAAAAGGTA[A/G]AATACAATTCCACCT	54542
rs553920405	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873228	GAGGTAGCAATATGT[A/G]TTTTTTAAACTGAAA	54542
rs553930157	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893285	ATTAACTTAAGTTAG[A/G]AGTTTGAGACCAGCC	54542
rs553942352	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122884593	CACGCTGGCTCATGC[C/T]TGTAATCCCAGCACT	54542
rs553955767	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872520	TGCTATGGCCAAAAT[C/T]GCTTATTTACATGTT	54542
rs554101969	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898440	AACAGTGAGAGAATT[C/T]TTCTTATTTCTGAGA	54542
rs554158033	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893907	CTTAACTGCTCCAAG[A/T]CATAATTTCCATATC	54542
rs554275926	in-del	-/C	0.00755907	0.0610114	intron-variant	RC3H2	GRCh38.p7	9:122894704	GCCAATATGGCGAGA[-/C]CCCCATCTCTACTAA	54542
rs554337978	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122862967	AGTTCATTATTTTAG[A/G]GTGTACAATTCAGTA	54542
rs554350401	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122900437	TAAGATAAATCAATA[C/T]AAAATTTTACCTAAA	54542
rs554364405	in-del	-/AAA			intron-variant	RC3H2	GRCh38.p7	9:122896136	AAAAAAAAAAAAAAA[-/AAA]CTTTACGAATTTGTG	54542
rs554545555	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865151	AAGTCACTTTCCCAC[C/T]TTCCAAGTTCACAGG	54542
rs554571200	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122863975	CGCCCAACCTCAGGT[A/G]ATCTGCCCACCTCGG	54542
rs554606130	snp	A/T	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122871387	ACTGCAAGCTCCACC[A/T]CCCAGGTTCACGCCA	54542
rs554633693	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122864631	AGTCCCCTCCTTTTT[C/T]TTTTTTTGAGACAGT	54542
rs554636516	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122878810	CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT	54542
rs554683824	snp	C/T	1.65855e-05	0.00287967	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880069	TGGGTCACCTGTTCG[C/T]TGCAAAACAATTGTC	54542
rs554746319	snp	A/G	9.93739e-05	0.0070482	synonymous-codon	RC3H2	GRCh38.p7	9:122865564	AGAAATGACATTTCC[A/G]GCTGTGGTTGTGACA	54542
rs554782491	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122893389	ATTCTAGCTACTCAG[A/G]AGGCTGAGGCAGGAG	54542
rs554868095	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900579	GAGCATATAAATGAA[C/T]CATGGAGCACTAAGA	54542
rs554874678	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872676	TGCAACCTCTACCTC[C/T]CAGGTTCACGCGATT	54542
rs554892973	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122876872	AAAAGACCAAAAGCC[A/G]TAAAAAGGATATATA	54542
rs555052579	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886851	ATTCAAGTTATTTAC[C/T]CACTTTTAAGTTAGG	54542
rs555086579	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891224	GATGGGGTTTTACCA[C/T]GTTGGCCAGGGTGGT	54542
rs555108395	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869882	GCCAACATCATCTTA[C/T]AGATAAGAGGAAAAC	54542
rs555145398	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122869370	GCAATGCCTTCACAA[C/T]AGTTTCCCTTTTAGT	54542
rs555213800	in-del	-/AT	0.00279162	0.0372561	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906981	TACATATATACATAC[-/AT]ATATAAATATATATA	54542
rs555273172	snp	C/G	1.9452e-05	0.0031186	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880845	TGTGCTTTCTCCCTT[C/G]AACTGATTCGTTTAT	54542
rs555354895	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883131	GCTAGGGCCTCTAGA[C/G]TGGGTAACATGAATT	54542
rs555397589	snp	A/T	0.000117192	0.00765391	intron-variant	RC3H2	GRCh38.p7	9:122890255	ACCGAGCTCCAGAAA[A/T]TGGCATCCTCAAGCC	54542
rs555493881	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122886054	ACCATGCCCAGCTAA[-/T]TTTTTTTCTATTTTC	54542
rs555554108	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862295	TCAAAAATTGGAACT[C/T]ATAGAAAAAGCTAAT	54542
rs555678384	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891827	ACAATTGTTTATTAT[A/G]CCTATGATGTGCTAA	54542
rs555680052	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899241	CCAAGTAACTGGGAC[A/G]GCACCCACCATCATG	54542
rs555826036	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881684	GGTGGGGATGGAGAG[A/G]ACAGGGTCTTTGTCA	54542
rs555875452	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122885218	GGAAAGGAGCATAAA[A/G]CAAGCAACCTACTCT	54542
rs555976809	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884705	TAAAAATATAAAAAT[C/T]AGCTGGGCATGGTGG	54542
rs556093896	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869466	CATTGGCAGAGGAAG[C/G]TGATGCTCAATAAAA	54542
rs556162897	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892540	CCTCAGCCTCCGGAA[C/T]AGCTGGAACTACAGG	54542
rs556210732	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884533	TGAAGTTAATCATTG[A/G]AGAACATCAGACAAA	54542
rs556259133	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122901799	GTTTCACCTGTGGGT[C/G]AGGCTGATCTCAAAC	54542
rs556291692	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883894	AGCTACTTTGGAGGC[A/G]GAAGTGGAGGATCAC	54542
rs556308724	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906785	ACGTTTCTTCCACAC[A/G]TTATCTTTTTCGTTC	54542
rs556330546	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122891270	CCAAATGATCTGCCC[A/G]CCTCGGCCTCTCAAA	54542
rs556342197	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899472	CTATGTAAAAAGCAC[C/T]CCTATACAAACTTTC	54542
rs556343202	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122850272	GAGCCACCACTCCTG[A/G]CTTGAAAAGTCCTGT	54542
rs556407155	in-del	-/ATTAA	0.00478085	0.0486577	intron-variant	RC3H2	GRCh38.p7	9:122857324	TACTGAAAACACCAG[-/ATTAA]ATTAAAATCATCCTG	54542
rs556437949	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122886082	TTCAGTAGAGACAGA[A/G]TTTTCCCATGTTGGT	54542
rs556488295	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878955	AGAGATGGGGTTTCA[A/C]CATGTTGGCCAAGCT	54542
rs556765537	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122851621	CCTGCCTCAGCCTGC[A/C]GAGTGCCTGCAATTG	54542
rs556811500	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878265	CAGCACAACCTTTTT[C/T]ATTTTTTATTTTTAT	54542
rs556850573	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122893137	AATTATCATGCATAG[A/G]TAATACATGAAAGCC	54542
rs556876552	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896285	GTTTTCCATATATAC[A/G]TCCCTACATAGACCT	54542
rs556981797	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122902813	CCCGAATGGTGCCAC[C/T]GCACTCCAGCATGGG	54542
rs557135691	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122882322	AGTGTCCAAGCCTCA[C/T]TAGTGGAGTTAAATG	54542
rs557317616	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854108	GAGGAGGGAAAAAAA[G/T]AAAAGTTAGCTTCCA	54542
rs557333793	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905680	CGTGGAATCCATTGA[A/G]CAGAATCTGATACAT	54542
rs557359278	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861162	CTAAGTAATCAGCTG[A/G]AAAGGATCTTATGGC	54542
rs557395945	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122860400	TTAGTCACCATTTAC[C/T]CATTCTTTTTTTTTT	54542
rs557449106	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852567	CCGGCCAGCCGCCCC[A/G]TCCGGGAGGGAGGTG	54542
rs557456657	snp	C/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122875032	TTTCTCAAAAGCTCC[C/G]CTTTTAGCTAAAAAG	54542
rs557464425	in-del	-/TCCATAAA	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122883564	AAATAAAACATACTT[-/TCCATAAA]TCCATAAATAAAACA	54542
rs557483732	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122867509	GGGGATGTGAGGGGC[A/G]CCTCTGCCCGGCCGC	54542
rs557500294	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876390	CCCAGTACTTTGGGA[A/G]GCCAAGGCAGGCAGA	54542
rs557685039	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905152	GGGCCGCTCCCGGGA[G/T]CCCCGCGACGGCGCG	54542
rs557751769	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122897838	ACATCAAAGCTTTTA[C/T]GTATTTTTCTCAACG	54542
rs557755718	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122889749	ATTTGTAAAACTGTA[A/G]CTATATTGCCTATCT	54542
rs557790760	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122896321	TTTCATTTACACTAT[C/T]ATATAAAAAGTCAAG	54542
rs557829431	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857631	CAGTGCTGGCATGAG[C/T]AGGTGCTCAATAAAT	54542
rs557907693	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868599	ACCCAGGGACACAAA[C/G]GCTGCGGAAGGCCGC	54542
rs558003333	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122860932	TTTTGTTTATTTTGA[C/T]AATTCCTATATCCCC	54542
rs558074898	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906466	AACCCGGGAGACGGA[A/G]GTTGCAGTGAGCCGA	54542
rs558089700	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891734	GGGATAAGTTTCTCA[A/G]TAAAATCACTATGGC	54542
rs558132218	in-del	-/TTTGT			intron-variant	RC3H2	GRCh38.p7	9:122885888	TTTTGTTTTGTTTTG[-/TTTGT]TTTGTTTTGTTTTGA	54542
rs558216978	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861213	AGTCAAATTTCGGCC[A/G]GGCACGGTGGCTCAC	54542
rs558288265	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122891303	GCTGGAATTACAGGC[A/G]TGAGCCTCTGTGCCC	54542
rs558331361	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122890163	ACAAAACAGCAATAA[C/T]AACAACAACAAAAAC	54542
rs558343492	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122885969	CTTCGCTCACTGCAA[C/G]CTCCGCCTCCTAGGT	54542
rs558428461	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876340	CCCACAAAGAGTTGA[C/T]AGACAGGGCAGGTGT	54542
rs558473121	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898157	TATAAGAGAAGACTG[C/T]GATGACTGAGAGATG	54542
rs558567640	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864707	TTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCATG	54542
rs558596880	snp	C/T	0.00318978	0.0398085	intron-variant	RC3H2	GRCh38.p7	9:122850736	GCCACTACGCCCAGC[C/T]TAGCCAAGAAAATCT	54542
rs558604500	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872423	AGTGATATGTCTAAG[A/T]CAAAATGAAAATTTC	54542
rs558630292	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856847	TCTCAGGGAAATACT[A/C]ATTTCCTGAAGCATA	54542
rs558650381	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865669	ATACCTGTTTCAAAA[A/G]CAATCAACAGATTGG	54542
rs558680016	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851918	TCTGCCCGGCCGCCA[A/C]CCCGTCTGGGAAGTG	54542
rs558683731	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122860249	AAAACACTTCAGACA[C/T]TGCCACATTGACAAA	54542
rs558688957	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122873417	ATGCAGGAAATATAA[A/G]GATGAAGAACCCTTG	54542
rs558694479	in-del	-/A	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122891698	AGATAGCTGTTCAAT[-/A]AAATGAATGAATGAA	54542
rs558741002	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894411	CATTCTAGTGGAGAG[A/G]AGAAGAGGTAGCCAA	54542
rs558776093	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901752	GCGCACCACCATGCC[C/T]GGTTAATTTTTGTAT	54542
rs558811970	in-del	-/C			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907148	TCACTGCAACCTCCA[-/C]CTCCTGGGTTCAAGG	54542
rs558832446	snp	C/T	0.000182347	0.00954674	missense	RC3H2	GRCh38.p7	9:122851405	CTATCAGGTTTAGTA[C/T]CTGTTGCATCTTCTG	54542
rs558880258	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874071	CCTAGGGAAGTCTGT[A/G]GAGGGAAGATAATAT	54542
rs558929235	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122867410	CCGGGAGGGAGGTTG[C/G]GGGGTCAGCACCCCG	54542
rs559028194	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900969	ATGAGTGCTGACACA[C/T]AAAACAGGAAGCACA	54542
rs559130581	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887768	TTTTTTTTTTGAGAT[A/G]GAGTTTTGCTCTTTC	54542
rs559151600	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893696	CAACTTTTTTGTAAG[G/T]CTGAAAGAATTTCAA	54542
rs559177901	snp	G/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122903358	AACCTTGTTATGAAG[G/T]TTTTTTTAGCGTTCT	54542
rs559205443	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122862648	ACCTGTAATCCCAGC[C/G]TTTTGGGAGGCCAAG	54542
rs559295595	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122851653	AGGCGCGCGCCGCCA[C/T]GCCTGACTGGTTTTC	54542
rs559304662	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865101	TTCTGGTCCAGTCTC[C/T]TTGGGAGAGTTGAGG	54542
rs559371541	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122897767	TGCCTGGAAACAATA[A/C]CTTAATAGTGTTCCT	54542
rs559429902	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850837	GCAACCAGATTAAAG[A/C]AGCATAACCTGATGC	54542
rs559451759	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122859347	TGATTCTCCTGGGCC[C/T]CCCAAAGTGCTGGGA	54542
rs559466727	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122850282	TCCTGGCTTGAAAAG[C/T]CCTGTTTTCCAAAAG	54542
rs559602236	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881002	TAATCCTTGCCTTCA[A/G]TGATTTCAGCCACTA	54542
rs559606536	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851966	GCCGCCCATCGTCTG[G/T]GATGTGAGGAGCCCC	54542
rs559638003	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880376	TTGAGACTTTGTAAG[C/T]CTCACTGCTTTTATG	54542
rs559643230	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122895352	TTTTTATTTTTTGTA[A/G]AGATGGGGTTTCGCC	54542
rs559903417	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861876	AAAGTAGGTACAAAC[A/G]TAAGGGTTTAGAGTA	54542
rs559913887	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873507	TGAGCTCAGGAGTTC[C/G]AGACCAGCCTGGGCA	54542
rs559988624	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122869586	TTTTTTTTTTTGAGG[C/T]GGAGTTTTGCTCGTC	54542
rs560000438	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122855074	GCCAAGATCACACCA[C/T]TGCATTCCAGTCTGG	54542
rs560049227	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122898125	TAGGAAGCAAAATGA[G/T]GCACTGAAAATCAAC	54542
rs560051050	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122895769	CTGGCTTTAATATGT[A/G]GCACATGATGTACAG	54542
rs560069084	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892080	AGTGAATTCAAATAA[G/T]GTACAAATTTCAAGA	54542
rs560089257	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894837	GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGT	54542
rs560091077	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903584	AATAACAGATCAGGG[A/G]TAACTCAAAGGATCC	54542
rs560129598	snp	A/G	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122878398	TCAGAGAGCTCCCAA[A/G]TAGCTGGGACTACAG	54542
rs560183087	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906242	ATGTAGGCTAGAAAA[G/T]GACCATGACGCCGGG	54542
rs560323368	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876694	GATCAATTTTTTGGT[A/G]AGGTCTCAAAAATGA	54542
rs560363257	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891482	AATCTCTGAAACCCA[C/T]CCCAATCAAATTTTT	54542
rs560441105	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871033	CTCCTACAGCTAGAT[G/T]ATATTGTTTCCCACT	54542
rs560457883	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122898955	ATTTCACAGGAATGT[C/T]TACCAACCCAAATAT	54542
rs560520956	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856337	GCTCACTAGCAGCCT[C/T]GACTTCCCAGGCTCA	54542
rs560555796	in-del	-/TTTGT	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122885887	TTTTGTTTTGTTTTG[-/TTTGT]TTTGTTTTGTTTTGT	54542
rs560587858	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885509	ATTAAACCAAGGTAA[A/C]GTATCTAGTTACCAA	54542
rs560611582	snp	G/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122863692	TTAACTAGACCATGT[G/T]CTCAAATATATCTTT	54542
rs560675990	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122892613	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATAG	54542
rs560710775	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857052	ATGGGTTAAAAAATA[C/T]AATGCCTAGGATTAC	54542
rs560725729	snp	A/G	3.36027e-05	0.00409881	synonymous-codon	RC3H2	GRCh38.p7	9:122855203	TACACTGATGGGCTT[A/G]GTCGCACTTCCTTGG	54542
rs560745244	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122901486	ATATGTGATTTTGCC[A/G]TTAACGTGTGAAGTA	54542
rs560748858	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864189	CTGATAGACTATTTA[C/T]AGGCAACAAAATCTG	54542
rs560796366	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907000	TAAATATATATACAC[A/T]TATATAGATACATAT	54542
rs560854444	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899000	AATTAGATGTTTAAA[A/C]ATGTAGTCACATTCA	54542
rs560897096	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885661	AGGACTTTTTTAAAA[A/C]TTGAGATAAAATTAA	54542
rs560904754	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856046	GAAATGGTATTTTTA[C/T]AATAGAAAATGGCAT	54542
rs560962142	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871574	GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	54542
rs560993699	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861925	GTGCTTATTCTTTAC[A/G]TAAAGTAAAATAGAG	54542
rs560995680	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122870192	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	54542
rs561001414	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871161	ATAAGGGACAATGAG[C/T]TCCTGTTCCTGACTA	54542
rs561009773	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122898621	AGACGTGGTGGCACA[C/T]GCCTGTAATTCCAGC	54542
rs561080286	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122854674	TCAGTGTACTGAGGT[A/G]AATGTATACTTCTCA	54542
rs561080956	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904939	AGAGAGGGGCCTCCG[C/T]AGGGCCCGGGTTCCA	54542
rs561127612	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122886452	GGTCATATGGTAATT[C/G]TTTAACTTTTTAAGG	54542
rs561204903	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867177	CCCGGCAGCCGGCCC[A/G]TCTGAGAAGTGAGGA	54542
rs561215690	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892168	CCCAGGTTGAGTGCA[A/G]TGGCACGATCACAGC	54542
rs561221051	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	RC3H2	GRCh38.p7	9:122849097	TAAGAACATCTAACT[C/T]CACTCTTCAAAATTA	54542
rs561265633	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878540	CTCCCAAAGTGCTGG[A/G]ATTATAGACATGAGC	54542
rs561276317	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861124	ATTATTTTTAACACA[A/G]AAGAATTTTCTTGGT	54542
rs561297103	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892279	ACCATGCCCAGCTAA[C/T]TTTTTGTATTTTTAG	54542
rs561331695	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850362	TGAAGATTAAGCCCA[C/T]ATTTTTGGCAGTAAT	54542
rs561371747	snp	C/G/T			intron-variant	RC3H2	GRCh38.p7	9:122887341	TTGCCCCACTTACAT[C/G/T]TAGTAGGAGCTCCTT	54542
rs561394875	snp	C/G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901043	AGAGCCAGCTAAATA[C/G/T]TTTCATTTTCTCTTA	54542
rs561415760	snp	A/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122857219	ATAATGAAAAGATTT[A/T]AAAAATTTTAATATC	54542
rs561519627	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901517	TATATGACTCAAATT[C/T]TACTTCTTAAATACA	54542
rs561535913	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857793	TATATTCAGTGTTTA[C/T]TGAACTAAACTCAAT	54542
rs561571750	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904622	CGGCCGTCCCCATCC[A/T]GGGAGGTTAAGCCCT	54542
rs561578429	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122882463	CCAACAAAATAACCT[A/C]AATAAGCTTTGGTTT	54542
rs561673905	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868269	ATTGAGAACGGGCCA[G/T]GATGACAATTGCGGT	54542
rs561674520	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889871	TATTGGCTGGGTGCA[A/G]TGGCTCACGCCTGTA	54542
rs561705065	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853707	CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA	54542
rs561721861	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905280	CGGCGGCGAAGGCCG[A/C]GACGGGGCCTCCTCC	54542
rs561735913	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122861240	TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC	54542
rs561811260	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890900	TTATCAAATTTTCCC[C/T]CTTTACTTGAACATT	54542
rs561849863	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122897721	TTTTTTAAAAAACCT[A/C]TTTGCTGAATTAATT	54542
rs561855375	in-del	-/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122871707	TTTTTCTCCTTTGTG[-/T]TTTTTTTTTCATACT	54542
rs561929413	snp	A/G	0.00676609	0.0577691	intron-variant	RC3H2	GRCh38.p7	9:122853007	TAGAAAGAAGTAGAC[A/G]TGGGAGACTTTTCAT	54542
rs561961838	snp	G/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882051	CTATGATGGCACCAC[G/T]GCACTCCAGCCTAAG	54542
rs562007252	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860699	CATTACAGGCATCAG[A/C]CACCGTGCCTGGCCA	54542
rs562157015	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122870568	GATATACACTGAATT[C/T]TTAGTATTGGGGCAG	54542
rs562241324	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868293	TTGCGGTTTTGTGGA[A/G]TAGAAAGGGGGCAAA	54542
rs562284257	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884065	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACCAGG	54542
rs562350997	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868937	GTTAAGTTCCACTCT[G/T]GTCGCCCAGGTTACA	54542
rs562386662	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122854478	AATGTGTACCCTTAA[A/G]ATACATACAAGTCTG	54542
rs562493907	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122870645	CTGCCTTAAATCCTA[A/T]ATGCAAGTGATCCTC	54542
rs562605180	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891991	TTAATGAATGACTGA[A/C]TGAATACATGCATAC	54542
rs562611645	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906024	GAATTATTCTTACAG[G/T]TTATAATTTATAGAT	54542
rs562634934	snp	C/T	0.000406146	0.0142446	intron-variant	RC3H2	GRCh38.p7	9:122875379	TACACTTATGTAAGA[C/T]AGACAAACATTTAAT	54542
rs562686258	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891417	AACTACTTAGCCAAT[A/T]GTAGATCACTACAAT	54542
rs562737755	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907188	GCCTTAGCCTCCCCA[A/G]TAGCTGGAATTACAG	54542
rs562756210	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122874593	TATAATCTCAGTTCA[C/T]GGCAGACCTGACCTC	54542
rs562809621	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905327	GCCTCCTCCTCCTCC[C/T]CCTCCTCACCACGGA	54542
rs562920175	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122876847	GAATACACAGGGAAA[A/C]AGAATGTTAAAAAGA	54542
rs563004966	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894638	TAATCCCAGCACTTT[G/T]GGAGGCCAAGGTGGG	54542
rs563034695	snp	A/G	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122870304	TGCTTGAGCCTGGGA[A/G]ACAGAGGTTGCAGTG	54542
rs563042394	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863582	ATATGTGTAAATGCT[A/G]TCTCCACAACTATAT	54542
rs563070774	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877601	ACAAAAATGGGAACA[A/C]ATTCAATGAGTGGCA	54542
rs563081947	in-del	-/AT	0.00755907	0.0610114	intron-variant	RC3H2	GRCh38.p7	9:122896068	GGCCATACTGGAAGA[-/AT]TGTCTTGGGCCACAC	54542
rs563083144	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862843	GAGGTTGCAGTGAGC[C/T]GAAATCGCACCATTG	54542
rs563104030	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870988	TTTTCCCATCTCCAA[C/T]AGCCTTTTCCCTTCC	54542
rs563157848	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880395	ACTGCTTTTATGCTA[A/G]TATCATGTATTTGTT	54542
rs563158095	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122894335	CACTGGACACAGTTA[C/T]AGGTACCAGGGATAT	54542
rs563442324	snp	C/T	0.000165599	0.0090979	synonymous-codon	RC3H2	GRCh38.p7	9:122858921	TGGTCCATACGGCTG[C/T]GGAGGAGGAGGCTGG	54542
rs563505008	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852669	CCAGCCGCCCTGTCC[G/T]GGAGGTGAGGGGCGC	54542
rs563518797	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904302	AGTGATTACTTGAGT[C/T]AATTTTGGTGTGAAG	54542
rs563595976	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122873587	GCATGGTGGCGTGTG[C/T]CTGTGGTCCCAGCTA	54542
rs563623954	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122889909	AACTTTGGGAGGCTG[A/G]GGCAGGCAGATCACC	54542
rs563634778	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881058	AAAATTATAGTAAAA[C/G]TTATAAGGCTTGATG	54542
rs563659980	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895906	AAAGTAGACCCTCAT[G/T]AAATATGTTATTTCA	54542
rs563684808	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122887013	CTTAAAACTTTGTAT[A/G]ATGGAAAATTTGCCT	54542
rs563692723	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122854129	TTAGCTTCCAACTAT[A/G]GCTTTCAACTGTCAT	54542
rs563712344	in-del	-/T	0.00517822	0.0506191	intron-variant	RC3H2	GRCh38.p7	9:122871638	AAATGTTGTATCTTC[-/T]AAGAGTCTTTCCTAC	54542
rs563803420	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122866730	TGCCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC	54542
rs563932461	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903824	TTTCTTCAAAAATTG[A/T]ACGTGGAAGTAAACA	54542
rs563933404	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889948	GGAGTTCCAGACCAG[C/T]CTGGCCAACATGGTG	54542
rs563934364	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887674	ACAATTGAGTCCGTA[C/T]TAATATTGCCAATTC	54542
rs563948101	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873769	ACACATGTAAATAAA[C/T]AATTATAATACTGTA	54542
rs564058820	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892680	CCTCCCAAAGTGCTG[A/G]GATTACAGGGGTGAG	54542
rs564099980	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860541	ACCTCAGCCTCCCAA[A/G]CAGATGGGACTACAA	54542
rs564136667	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122867865	AGGAGCGTCTCCGCC[C/T]GGCAGCCACCCCGTC	54542
rs564210149	snp	A/G	0.00199481	0.0315187	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905231	GTTTCACGACCTCAA[A/G]CTCCATCGGGAGCTA	54542
rs564237556	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852275	GCAGCCGCCCCGTAT[C/G]AGAAGTGAGGAGCCT	54542
rs564302550	snp	G/T	0.00159617	0.0282053	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897576	TGTAGTGTTTTGTAA[G/T]CTAGAAATGGACAAA	54542
rs564403860	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122866803	CCCAAAGTGCTGAGA[C/T]TGCAGCCTATGCCCG	54542
rs564442341	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874541	TTATATTTTTGAGAC[A/G]GAGTCTTGCTCTGCT	54542
rs564483921	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890001	AGAAAAATTAGCCGG[C/G]TATGATGGCGTGTGC	54542
rs564513797	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853667	TGAGGCAGGAGAATC[A/G]CTTGAACCTGAGAGC	54542
rs564549725	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852971	AAAAGATTGAGAAAT[C/T]GGATGGTAGCCGTGT	54542
rs564693063	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876174	GCTAAGGAAGGACAG[C/T]TGACAAATATGATTA	54542
rs564708161	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892703	GGGGTGAGCCACCGC[A/G]CCCGGCTCTAGCTTG	54542
rs564729895	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122883468	TGGGTATTAGAGTTT[A/G]TAGTGGCCCATTACC	54542
rs564797209	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122899844	TGTAGTTTTTCATAA[C/T]GGCCACCTGTTTGGA	54542
rs564809933	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882766	CTGGTTGTATCTGAG[A/G]TAACATGTAGGCCAT	54542
rs564852428	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850143	CACCACGCCCAGCTA[C/T]TTTGTATTTTTAGTA	54542
rs564880978	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122900887	AGGAGTGAGAAATGC[C/T]AAATTAAAGGTGGGA	54542
rs564907038	snp	G/T	0.000137604	0.00829354	intron-variant	RC3H2	GRCh38.p7	9:122857881	TTGAAGTCAGCTGTT[G/T]GACCTATCCCTGCAA	54542
rs564948087	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122895387	TGTCCAGGCTAGTCT[C/T]GAACTCCTGGCCTCA	54542
rs564956508	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856230	CACAGAGATCACAGT[C/T]CATATCCTAAAGGAG	54542
rs565101495	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122879367	TCACTGCACTCCAGC[A/C]TGGGTGACAGAGTGA	54542
rs565134682	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886289	ATACATTACATTTTG[C/T]TTATCCATTTATCAC	54542
rs565136694	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881052	AAGTAGAAAATTATA[C/G]TAAAAGTTATAAGGC	54542
rs565217392	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851020	AAAAATTAATTTCGC[A/G]TTTTTTTCTCTTTAT	54542
rs565232351	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122865801	AAATAATCAAATACA[A/G]TCTATATCAAATTCT	54542
rs565365544	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122867154	CTGAGAAGTGAGGAG[A/C]CCCTCCGCCCGGCAG	54542
rs565378839	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872830	ACCTCAAGTGATACA[C/T]CAGCCTTGGCCTCCC	54542
rs565410588	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894188	GCCGTGAACCTGGGA[A/G]GCAGAGCTTGCAGTG	54542
rs565425452	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892256	AGCTGGGACTACAGG[C/T]GTGTGTCACCATGCC	54542
rs565446535	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122901644	TTGCCTAGGCTGGAG[C/T]GCGGTGGTGCGATTT	54542
rs565460205	snp	C/T	0.0023933	0.0345097	intron-variant	RC3H2	GRCh38.p7	9:122894732	TAAAAATACAAAAAT[C/T]ATCTGGGCATGGTGG	54542
rs565543163	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902222	AGGCGTGAGCCACCG[C/G]GCCCAGCCAACTTTC	54542
rs565548849	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892599	TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACCGT	54542
rs565660983	snp	G/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122878801	TCGCCCAGGCTGGAG[G/T]GCAGTGGCGCGATCT	54542
rs565682770	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122859584	TTTTTGGGAGCAGAC[A/G]TTAAAGACCTCTTTC	54542
rs565731931	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122885958	AGTGGCACGATCTTC[A/G]CTCACTGCAACCTCC	54542
rs565740249	snp	C/T	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122891144	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	54542
rs565754384	in-del	-/CT	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122872143	TGGCCAAGAGAACCA[-/CT]GATTTTCTGCCCTGA	54542
rs565768070	snp	A/G	1.65894e-05	0.00288	intron-variant	RC3H2	GRCh38.p7	9:122892876	GTACTACCAAGTCCT[A/G]CTTATCAGTAAAAAT	54542
rs565790020	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863960	CAGGCTGGTCTTGAA[C/T]GCCCAACCTCAGGTG	54542
rs565796322	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872812	GCTGGTCTCAAACTC[C/T]TGACCTCAAGTGATA	54542
rs565915680	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122873248	TTAAACTGAAAGGAC[A/G]GTCACATCACCTACT	54542
rs566107588	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893939	GCAAAATGAAGATGA[A/C]AATCTGTATTTTGTA	54542
rs566122866	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881263	AGGCCGAGGTGGGCA[C/G]ATCACTTGAAGTCAG	54542
rs566130895	snp	C/T	0.000745163	0.019288	intron-variant, missense	RC3H2	GRCh38.p7	9:122853947	GAAAGGTTCAGTTTC[C/T]TTACCTCTCCATTTC	54542
rs566191631	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901124	AAATGCCAGAATAAA[C/G]TTTATGCTTCTTTAA	54542
rs566192943	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857513	ATCTTGGGCAAATTA[C/T]TTAACTTCTGTAAGA	54542
rs566222408	snp	A/G			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849052	AATGCAGTAAAGAAT[A/G]CTAGTATATAACCCT	54542
rs566265981	in-del	-/CCTCTGCCCGGCCGCCTATCGTCTGGGACGTGAGGAGCC			intron-variant	RC3H2	GRCh38.p7	9:122867510	GGGATGTGAGGGGCG[lengthTooLong]CCTCTGCCTGGCTGC	54542
rs566279518	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122855507	GTTAATTTAAAACTA[A/G]CTCTAGACTCAACGA	54542
rs566307068	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122876407	CCAAGGCAGGCAGAT[A/C]GCTTGAGGTCAGGAG	54542
rs566330451	snp	G/T	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880765	CTCCTTCAGCTGCAT[G/T]AGGGAAGAGTCTTCA	54542
rs566365229	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122887319	GTCATTCATTATGAT[A/G]TTTAAATTGCCCCAC	54542
rs566471362	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860900	GCTGAAATATGAACT[C/T]CTTGAGGAAAGGCCA	54542
rs566480309	snp	A/C/T	0.00119737	0.0244387	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906479	GAGGTTGCAGTGAGC[A/C/T]GAGACCGCGCCATTG	54542
rs566489465	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122897164	AATTTGTGTTGGGCC[A/G]CATTCAAAGATGTCC	54542
rs566543040	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870372	AGAGCAAGACTCTGT[C/G]TCCAAAAACAAACAA	54542
rs566586940	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122904850	TCGTTAGGGGTCAGA[A/G]GCGTCCGCTCGGCCA	54542
rs566639619	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884290	AATGCGAGACTCCGT[C/T]TCTAAAAAAAAAATT	54542
rs566657834	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122903890	TAGCTTTTTAGACAG[C/T]TAAAAGGTTTTTTAA	54542
rs566712744	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122900009	GGGGAGTTTCAACCA[C/T]ACAGAAAAATGCTAT	54542
rs566911974	in-del	-/CA	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122888706	ACTGGAAGGATATAC[-/CA]CAGTTTATTATACTA	54542
rs566961357	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867249	GGGGATCAGCCCCCC[A/G]CCCGGCCAGCCGCCC	54542
rs566994751	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869338	TATGGTAATTAAATA[C/T]AAAGTGTTAGTAGTA	54542
rs567027024	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122898834	AACACACTAAACTTC[C/T]CAGAATTTCTTTATC	54542
rs567044591	snp	A/G	0.000198153	0.00995175	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849593	TGTAAATGCTTCCAT[A/G]GTGTGGTCACAAATT	54542
rs567127095	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122863979	CAACCTCAGGTGATC[G/T]GCCCACCTCGGCCTC	54542
rs567143288	snp	A/G	3.32585e-05	0.00407776	intron-variant	RC3H2	GRCh38.p7	9:122855722	CCCTGCAACCCCAGC[A/G]AAATCATACCATTAA	54542
rs567145119	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869900	ATAAGAGGAAAACCA[A/G]TAATTACTTCTTTCA	54542
rs567178461	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863025	AATTATCACCACTAA[C/T]TCTGAAACATTTTCA	54542
rs567255446	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891601	ACACATGATTACTCA[A/T]TACTCCTTTAAAACA	54542
rs567320366	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899417	ATTCACAAAAACAGA[G/T]ATTAAAAAAAATCTT	54542
rs567339423	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863762	TTTTTTTGAGATGGA[G/T]TCTCACTCTTGTTGC	54542
rs567344649	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898686	TGTGGAAGGCGGAGA[C/T]TGCAGTGAGCCGAGA	54542
rs567348698	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122866245	AACATTTGTATGAAA[C/G]ATTTTTCTGATACTA	54542
rs567377989	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863164	TTCTGGACATTTAAC[A/G]TAAATGTGACCTTTT	54542
rs567381653	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898056	TTGTAGAGACTCAAG[C/T]GTGAAGAAAACAGCT	54542
rs567407355	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877106	GGCAGAGTCTTGCTG[C/T]GTCCCTCAGGCTGGA	54542
rs567412169	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122863731	CTTGCCCAGGGAAGA[C/T]TGTAAAAGTCCTTTT	54542
rs567463764	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870465	TGCTCTAGAAAGCAA[A/T]AAATAAAGTTTTAAC	54542
rs567507516	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886044	AGGTGTGCACCACCA[G/T]GCCCAGCTAATTTTT	54542
rs567511789	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885010	AGTGATCTTGAACTG[C/G]ATCTCACACTTGAAT	54542
rs567570273	snp	A/C/G	4.9999e-05	0.00499974	missense	RC3H2	GRCh38.p7	9:122855832	CAGGGAGAATAATGG[A/C/G]AAAGATGATCTTCTT	54542
rs567594593	snp	C/T	1.752e-05	0.00295968	intron-variant	RC3H2	GRCh38.p7	9:122893052	AAAAAAAAGGAATAT[C/T]GCAGAAATACATTCA	54542
rs567735216	snp	A/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122866878	CCTATCGTCTGGGAC[A/G]TGAGGAGCCCCTCTG	54542
rs567858470	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873878	ACAGGAGTATAGTGG[C/T]GCCATCTCGGCTCAC	54542
rs567863802	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895973	CAAACATGAATTCTA[C/T]AGCACATGTTCTTTT	54542
rs567902663	in-del	-/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122866373	CTCTCCCCCTCCCCC[-/T]TCCCCCCTCCCTCTC	54542
rs567904672	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896904	GGTGATGTGGGCCTA[C/T]AGTCCCAGCTACTTG	54542
rs567913553	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878300	GAGACGGAGTCTTGC[C/T]CTGTTGCCCAGGCTG	54542
rs567944202	snp	C/G	1.6679e-05	0.00288777	missense	RC3H2	GRCh38.p7	9:122849770	TGCTAATAGACACTG[C/G]GAGTGGCTGGCTAAA	54542
rs567986884	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896184	AGCTGTCCTGGGCTG[C/T]ATGTGGCCTGAAAGC	54542
rs568025698	snp	G/T	0.00279162	0.0372561	intron-variant	RC3H2	GRCh38.p7	9:122903897	TTAGACAGCTAAAAG[G/T]TTTTTTAAAAAGGAG	54542
rs568236043	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122889427	TTTTGCTTTTTCCGC[A/G]TTTTGATCTAGTTGT	54542
rs568252463	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884689	GAAACCCCATCTCTA[C/T]TAAAAATATAAAAAT	54542
rs568291990	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122859830	AAGGATTAATTTTTT[A/T]AAATGTAGACATTCT	54542
rs568444107	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875650	CTGGTTAGTATGAAG[C/T]GTCAGGGGAATTACC	54542
rs568456850	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122875034	TCTCAAAAGCTCCCC[G/T]TTTAGCTAAAAAGCT	54542
rs568465316	snp	A/G	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122890050	AGGGGGCTGAGTCAG[A/G]AGAATTGCTTGAGCA	54542
rs568520486	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860803	TCTCAACCGAAAAAA[C/T]ATAGTCCATTAGTGG	54542
rs568543765	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882125	AGAAATGTTCTGCTA[C/T]CAGAGAAATTATCAT	54542
rs568560867	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905591	ATGGGAAATTCCCTG[C/T]ACATTCATCTGCGCC	54542
rs568608358	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122860190	TATGACTGTCCTCCT[A/T]ACTAGAAATTTTTAA	54542
rs568645006	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122867020	TTGCCCCACCGCCCC[A/G]TCTGGGATGTGAGGA	54542
rs568698332	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882904	TTTCAAGACACTAAA[G/T]GTAAAGAAATGAGGC	54542
rs568726209	snp	C/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122869144	ATCCTGACCTCAGGT[C/G]ATCTGCCCACTTCGG	54542
rs568757105	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122904722	TCTCGGGAAGCCCCA[A/G]GGCAGAAAGCTGAAA	54542
rs568782089	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122890109	CTGCGCCACTGCACT[C/G]CAGCCTGGGTGACAG	54542
rs568811531	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876266	GGAAGGCAGGAGGAG[C/G]AGGTATGGGAGAAAA	54542
rs568813545	snp	C/G	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122868343	AATCGGATGGTTGCC[C/G]TGTCTGTGTGGAAAG	54542
rs568832164	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896292	ATATATACATCCCTA[C/T]ATAGACCTTATTGTT	54542
rs568838739	snp	A/G	0.0718919	0.175435	intron-variant	RC3H2	GRCh38.p7	9:122852408	CCGGGAGGGAGGTGG[A/G]GGGGTCAGCCCCCCG	54542
rs568866927	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122903943	TTAATATCGTAAAAA[A/G]CTTTTAACTAAGTTT	54542
rs568896805	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856866	TCCTGAAGCATAATT[A/G]TATATCAAAAAAGAA	54542
rs568935122	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889732	TCTAACTTGGTTTTC[C/T]AATTTGTAAAACTGT	54542
rs569059136	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122883562	GCAAAATAAAACATA[C/G]TTTCCATAAATAAAA	54542
rs569063057	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122896969	AGGTGGAGGTTGCAG[C/T]GAGCCCAGATCACGC	54542
rs569077977	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122876473	TCTCTACTAAAAATA[C/G]AAAAATTGGCCAGGC	54542
rs569181349	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869298	TATATGCCTAAAGTA[A/G]TGTTATTAATGTTAT	54542
rs569215982	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876352	TGATAGACAGGGCAG[C/G]TGTGGTGGCTCACGT	54542
rs569313851	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122888369	AAGTTGTTTTATAAT[G/T]ACATAAAATATTTAT	54542
rs569382307	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906457	AATCACTTGAACCCG[A/G]GAGACGGAGGTTGCA	54542
rs569383648	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875956	TGGTATGAGTAAATC[C/T]GTGCTTTTAAAATAT	54542
rs569481982	snp	A/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122854802	TTTCACAAGTTGGGG[A/T]TTAAAAAGCACAGTG	54542
rs569552012	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905690	ATTGAGCAGAATCTG[A/T]TACATCTGTGTCACA	54542
rs569561213	snp	G/T	1.65822e-05	0.00287938	intron-variant	RC3H2	GRCh38.p7	9:122854114	GGAAAAAAAGAAAAG[G/T]TAGCTTCCAACTATA	54542
rs569566324	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122869714	CACATTATAGGCGCG[C/T]GCCTGCCAACACACC	54542
rs569567216	snp	C/T	0.00795532	0.062565	intron-variant	RC3H2	GRCh38.p7	9:122861968	ATGATTAGGATTTCC[C/T]TAAAACAATAACTAA	54542
rs569574342	snp	A/T	0.0248432	0.108648	intron-variant	RC3H2	GRCh38.p7	9:122868339	GAGAAATCGGATGGT[A/T]GCCGTGTCTGTGTGG	54542
rs569592489	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122857347	AAAATCATCCTGGTA[C/T]ACAAACTTGTTTGGT	54542
rs569656632	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122890765	ACCTAAAAGTAAAAA[G/T]GACTCTATTTTTTAA	54542
rs569656696	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122854681	ACTGAGGTGAATGTA[C/T]ACTTCTCAAAATAGA	54542
rs569695977	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122878855	CCGGGTTCAAGCGAT[C/T]CTCCTGACTCAGCCG	54542
rs569828787	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901705	CATACGATTCTCCTG[A/C]CTCAGCCTCCTGAGT	54542
rs569920055	snp	C/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906205	TACAATGTACCCCTT[C/G]TTACTGATGAGAAAC	54542
rs569936485	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122866506	CTGCAACCTCCCTGC[C/T]TGATTCTCCTGCCTC	54542
rs569960369	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865133	AAACAAAACTCAGAG[G/T]TAAAGTCACTTTCCC	54542
rs569997192	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864653	TGAGACAGTGTCTCA[C/T]TCTGTTGCCCAGGCT	54542
rs570046499	snp	C/T	0.000819168	0.0202216	intron-variant	RC3H2	GRCh38.p7	9:122851687	TTTTTTTGGTGGAGA[C/T]GGGGTTTCGCTGTGA	54542
rs570060721	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902321	CTGCCTATCAAATCA[C/T]AGCCAATGGATAACT	54542
rs570087371	in-del	-/CTGTGTTCCAATAACAACTGGAACAA	0.0130921	0.0798413	intron-variant	RC3H2	GRCh38.p7	9:122862541	GAATTATTCTTTTTC[-/CTGTGTTCCAATAACAACTGGAACAA]CTGTGTTCCAATAAA	54542
rs570138914	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894918	TGGAGACAGACTGAA[C/T]GTTCTAGGCAAAGGT	54542
rs570173374	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122874655	CCTGAGTAGCTAAGA[C/T]GACAGGCGTATGCCA	54542
rs570211858	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881936	GAATCCAGCTAATAG[A/G]TAGGCATATATTACC	54542
rs570431100	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901837	CTCGTGATCTGCCCA[C/T]CTTGGCCTCCCAAAG	54542
rs570450303	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122865263	AAAATTCTGATTAAC[C/T]GGTATTCATCAGCAG	54542
rs570492280	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872424	GTGATATGTCTAAGA[C/G]AAAATGAAAATTTCA	54542
rs570662225	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851759	CAGCCTCGGCCTCCC[C/G]AGGTGCCGGGATTGC	54542
rs570691101	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122866025	GTTATGTAAAAATGA[C/T]AGGAACTGGCAACAA	54542
rs570747130	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851561	AGCCGAAGCTGGACT[A/G]TACTGCTGCCATCTC	54542
rs570930007	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888312	TAGCTTTATTTTTAG[C/G]TATTATTTTGATCAT	54542
rs570970513	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868335	GATTGAGAAATCGGA[C/T]GGTTGCCGTGTCTGT	54542
rs571075738	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122867424	GGGGGGTCAGCACCC[C/T]GCCCGGCCAGCCACC	54542
rs571109014	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122875515	CTGCTGAGTGGTTGT[A/C]ACAGATTCTGTGGCC	54542
rs571133039	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122863388	ACCAACCTATCTAAC[C/T]TTATTTTATACCAGT	54542
rs571166782	snp	C/T	0.00398564	0.0444627	intron-variant	RC3H2	GRCh38.p7	9:122862785	CTGTAATCCCAGCTA[C/T]TTAGGAGGCTGAGGC	54542
rs571202040	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874798	CTGCTGGGAATACAG[A/G]CATGAGCCACTACAC	54542
rs571273236	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850447	ATCTATAGATAGATA[A/G]ATAGATAGATAATTT	54542
rs571293197	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892322	TTCGCCTTGTTGCCC[A/T]GGCTGGTCTCAAACT	54542
rs571373104	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891687	TCCACGCTCTTTAGA[C/T]AGCTGTTCAATAAAT	54542
rs571404756	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122893551	AACAGCAGGAGCTGT[A/G]TGGATTAATGAAGGA	54542
rs571406072	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856622	TGATAAATTATGCAG[A/T]ATCAAAGAACAAAAG	54542
rs571443830	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871207	CCTGTGGCCTAGGTC[G/T]CAAGCCCATTTGCCT	54542
rs571492098	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887232	TGAATTCAGCTAAAA[G/T]AGGAAACTTTCCTCA	54542
rs571499308	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122877856	AACAGAATGCCCAGA[A/C]AAAGAAAATATTTTT	54542
rs571542116	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893169	TTTAAGTAAAATTAA[A/G]GTCAAACACCTAGCC	54542
rs571552554	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122849929	CTTTAGGAGTCTCTA[A/G]CAAAGACATGTCTTT	54542
rs571564189	snp	A/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122894153	AGTCCCAGTTACTCC[A/G]GAGGCTGAGGCAGGA	54542
rs571574357	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122886600	AGGCCGAGATGGGAG[A/G]ATCACTTGAAGCCAG	54542
rs571607852	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122901071	TTATTAGTCCACCAT[A/T]TTATGCAGCCAGTTC	54542
rs571680542	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122896371	AACAACAACAAAAAA[A/T]CCTGTTTCTGGTCAA	54542
rs571780113	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122854875	TTGCGAGGCTGAGGC[A/G]GGTGGATCACATGAG	54542
rs571913272	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893878	TACTTCTATGAATGA[A/C]CTTGAGTAAATTACT	54542
rs571925852	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862681	GGGCAGATCACTTGC[A/G]GTCAGGAGTTCTAGA	54542
rs571931171	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RC3H2	GRCh38.p7	9:122849069	TAGTATATAACCCTG[G/T]AAAATTCTATGGTAA	54542
rs572051192	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870608	GCCTTTTCAGGGACA[G/T]GATCTCACTATGTTG	54542
rs572078780	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122888844	AGATTCCTAGAAGTG[A/G]GATTGCTAGACCAAA	54542
rs572079044	in-del	-/GCTCACTGCAACCTCCCT	0.0126979	0.078662	intron-variant	RC3H2	GRCh38.p7	9:122866485	ACTGCTGCCATCTCG[-/GCTCACTGCAACCTCCCT]GCTCACTGCAACCTC	54542
rs572139260	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870146	TTGGGAGGCTGAGGC[A/G]AGTGGATTACCTGAG	54542
rs572146089	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892628	GTGTTAGCCAGGATA[C/G]TCTCGATCTTCTGAT	54542
rs572176031	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122877323	CTCCTGCCTCAGCCC[C/T]GCAAACTGCTGGGAC	54542
rs572222763	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122900469	CATAGAAGAAACTTC[A/G]TTCCTTCAAAACAGG	54542
rs572241172	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122849949	GACATGTCTTTATCA[A/C]TAGAAGTATCAGAAG	54542
rs572258945	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856031	AACTGTAATAAGCAA[A/G]AAATGGTATTTTTAC	54542
rs572307084	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899633	GTTTCCTTCCAACTT[G/T]AGAGATAAGCACTGA	54542
rs572339645	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886645	CAGTGGGCTATAAGC[A/G]TGCCACTGCACTCCA	54542
rs572347016	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863487	AATCCATGTTATGTT[G/T]TTTTTTTTCTGTAAT	54542
rs572369737	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122872551	TACTGTTCCTCTTTT[C/T]CCATTAGAAACATCT	54542
rs572457140	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885603	ACTTTTAAAATTCTT[C/T]AAATTTTTTCTTTTT	54542
rs572498669	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882414	AAGAAACATTTTTCT[A/G]TCTGTACTATTTTCA	54542
rs572516412	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122893352	TACAAAAATTAGCCA[A/G]GTGTGGTGGTGGATG	54542
rs572564170	in-del	-/A	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122896342	AAAGTCAAGTGAAGT[-/A]AAAAAAAAGTAACAA	54542
rs572581550	snp	A/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122864788	ACCATGCCCGGCTAA[A/T]TTTTTTTTTGTATTT	54542
rs572598460	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122886138	CAAGTTATCCACCCG[C/T]CTCGGCCTCCCAAAG	54542
rs572618419	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864354	AAGGAAATCTTATGC[C/T]GACACTCAGTAACAA	54542
rs572638301	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122852605	CAGCCCCCGGCCCGG[A/C]CAGCCGCCCTGACCG	54542
rs572653833	snp	A/G	0.000399281	0.0141238	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880018	GTCTATGTTTGCAAG[A/G]AGCTCTAAATGAGGC	54542
rs572764966	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876028	AGAGATTTAAGACTA[C/G]TGAGAAGGCAACAAG	54542
rs572864386	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122896323	TCATTTACACTATTA[C/T]ATAAAAAGTCAAGTG	54542
rs572928233	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868711	CTGCCAAATCCCCCT[C/T]TGTGAGAAACACCCA	54542
rs572940888	snp	C/T	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122897584	TTTGTAAGCTAGAAA[C/T]GGACAAAAGTATGAA	54542
rs572977715	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905255	GGAGCTACAGGGACA[A/G]CCCCGTTGGCGGCGG	54542
rs573014424	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899722	TTTGCAGAGTTATAC[A/G]AGAAAAGGCCTTTGA	54542
rs573058985	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868228	GCCCGGCCACCACCC[C/T]GTCTGGGAGGTGTAC	54542
rs573296516	snp	A/G	0.00199481	0.0315187	intron-variant	RC3H2	GRCh38.p7	9:122861219	ATTTCGGCCGGGCAC[A/G]GTGGCTCACACCTGT	54542
rs573297813	snp	G/T	1.67038e-05	0.00288992	missense	RC3H2	GRCh38.p7	9:122854242	CTTTCTATGACCAGA[G/T]AAATCAGTAACAATG	54542
rs573334718	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853694	GAGCCAGAGGCTGCA[C/G]TGAGCCAAGATCGTG	54542
rs573383976	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122884033	GGCGCGGTGGCTCAC[A/G]TCTGTAATTCCAGCA	54542
rs573410022	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891755	TCACTATGGCCACAT[A/G]CACAACAGTGCAAAG	54542
rs573473826	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891379	GAGTTGTCTATACTC[A/G]CTATTTCCTAGTCTA	54542
rs573539469	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122876080	AGCTTGGATCACAAG[A/G]ATGGAAAGAAGAATA	54542
rs573568178	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122883763	GAGGCAGGACGACTG[C/T]TTGAGCCCAGGAGTT	54542
rs573645003	snp	A/G	0.00835141	0.0640778	intron-variant	RC3H2	GRCh38.p7	9:122868837	ACAATATTCCCTCCT[A/G]TATGTGTGTGTGTGT	54542
rs573691723	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122863163	ATTCTGGACATTTAA[C/G]ATAAATGTGACCTTT	54542
rs573692137	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891873	ATTTCAGTTTTGTCA[G/T]AGACTTAAAATAATT	54542
rs573712118	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905941	GCAAAAATAAAAAAT[G/T]TAAGCACAAATTCTG	54542
rs573730769	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122898811	AGTAGCAAAACGATA[C/T]TAATTTGAACACACT	54542
rs573750961	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122897125	TCACAAAAAAAATCT[C/T]ACAATGTTTTAAGGA	54542
rs573776369	in-del	-/T	0.00398564	0.0444627	intron-variant	RC3H2	GRCh38.p7	9:122850609	ACTATGCCCAGCTAA[-/T]TTTTTTTGTATTTTT	54542
rs573828555	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862297	AAAAATTGGAACTTA[C/T]AGAAAAAGCTAATCT	54542
rs574072894	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854925	CCTGGCCAACATGGC[A/G]AAACTAAAATACAAA	54542
rs574077343	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122890012	CCGGGTATGATGGCG[C/T]GTGCCTGTAGTCCCA	54542
rs574080422	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122854376	GAAAACTTCACTCAT[C/T]GTTCCAAATTTAAAT	54542
rs574092024	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894585	ATGAATGAATAAAGA[A/C]CATGAAGAGAGAGGC	54542
rs574153560	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122899106	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTCAG	54542
rs574159474	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122878230	GTACAAAGTGTAGGT[C/T]TGATCCCAGCTCTTA	54542
rs574225474	snp	C/T	0.000199707	0.00999068	intron-variant	RC3H2	GRCh38.p7	9:122877447	AAAATTAAACCCATA[C/T]GAAACAGAATTCTCA	54542
rs574225587	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122891563	AGTTCCTTATTTTAT[C/G]TGACCTTCCAACAGC	54542
rs574249627	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122885254	GGTTCAGAAGAGAGG[A/G]AAAGAATAACAAATA	54542
rs574258127	snp	A/G	0.00795532	0.062565	intron-variant	RC3H2	GRCh38.p7	9:122884706	AAAAATATAAAAATT[A/G]GCTGGGCATGGTGGC	54542
rs574402389	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122895364	GTAGAGATGGGGTTT[C/T]GCCATGTTGTCCAGG	54542
rs574407008	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905713	GTGTCACATTCTTCT[G/T]CACACTCCTGTGATG	54542
rs574518286	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857781	CCGTAGTGCATTTAT[A/G]TTCAGTGTTTATTGA	54542
rs574530871	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881630	GGAATTTGGATATTA[A/T]TATGAAGGGAATGTG	54542
rs574542256	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850847	TAAAGAAGCATAACC[C/T]GATGCTGGAACACAG	54542
rs574562848	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122868381	CATGGGAGACTTTTC[A/G]TTTTGTTCTGTACTA	54542
rs574616943	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888374	GTTTTATAATTACAT[A/T]AAATATTTATGTGGT	54542
rs574647214	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122865937	ACTTTGTCCAAGAAT[A/G]TATTCAAAAAAACCT	54542
rs574796250	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122859451	ATTCAACACTTTGCT[A/G]AAGTGCTCCTTAAAA	54542
rs574851892	in-del	-/A/C	0.00994328	0.0699023	intron-variant	RC3H2	GRCh38.p7	9:122896096	CACATAAGATACACT[-/A/C]AACACTAACAATAGC	54542
rs574865388	snp	A/C	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122867471	TGGGGGGGTCAGCCC[A/C]CCGCCCGGCCAGCCG	54542
rs574890686	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122888764	GTTGTTTCCAGATGT[C/T]TGCTATTACAAATAG	54542
rs574909880	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899033	GAGAAAAAATATATA[A/G]CAGAAAGTATTCTCA	54542
rs574953060	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874930	TGAAGGTATGAGAAA[A/G]AAGAAAATGGATTTT	54542
rs575011535	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905122	TACCTGAGGGGGCCC[A/G]GGCGGGGTCGCTAAG	54542
rs575085216	snp	A/G	1.67178e-05	0.00289113	missense	RC3H2	GRCh38.p7	9:122897283	TGAATGCTTACCTGG[A/G]CTCCAACTAACTGGA	54542
rs575086781	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889880	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCTAGAA	54542
rs575169649	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122882329	AAGCCTCATTAGTGG[A/G]GTTAAATGAATTCAC	54542
rs575183061	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122889579	CTTGGTATAGGTGAA[C/G]ATTTTTTAAGACAGA	54542
rs575223502	in-del	-/ATAAGATG	0.0217236	0.101931	intron-variant	RC3H2	GRCh38.p7	9:122896733	TGCCATTAAAGCCAC[-/ATAAGATG]ATAAGATGGCTGGGT	54542
rs575240402	snp	A/G	0.0205511	0.0992634	intron-variant	RC3H2	GRCh38.p7	9:122851910	TTGCAGCCTCTGCCC[A/G]GCCGCCACCCCGTCT	54542
rs575251561	in-del	-/AA	0.00159617	0.0282053	intron-variant	RC3H2	GRCh38.p7	9:122889459	CCAACATCACTTATT[-/AA]AAGTTTCCTTTCCAA	54542
rs575305245	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122900825	TTGTATTAACTAATT[G/T]TAGTTACCAGTTACA	54542
rs575325233	snp	C/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122851622	CTGCCTCAGCCTGCA[C/G]AGTGCCTGCAATTGC	54542
rs575363827	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122894116	TACAAAAAATTAGCC[G/T]GGCGTGGTGGCGGGC	54542
rs575428935	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867169	CCCCTCCGCCCGGCA[A/G]CCGGCCCATCTGAGA	54542
rs575506380	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905158	CTCCCGGGAGCCCCG[C/T]GACGGCGCGGCTTGG	54542
rs575577459	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873554	TCTCTACAAAAAATA[C/T]AAAAAAAATTTAGCC	54542
rs575638203	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904519	AAAGGAAAAATGAGA[C/G]AGGGAAAGAAGAAAG	54542
rs575640902	snp	A/G	0.00199481	0.0315187	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905148	CTAAGGGCCGCTCCC[A/G]GGAGCCCCGCGACGG	54542
rs575654518	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122868554	GGCAGCATGCTCGTT[A/C]AGAGTCATCACCACT	54542
rs575658803	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122861792	TCACAGATTAGTCTA[C/G]CAGATGTTTACTTCT	54542
rs575699930	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122885390	AATTACAAATACATG[A/G]TTATTAATCAAAACA	54542
rs575722960	snp	C/G	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122852849	GGAAGTGAGGAGCCC[C/G]TCTGCCCAGCCACCA	54542
rs575780782	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122885842	CAACACTAGCTGGCT[A/G]TCTGGTTTCTTTCAT	54542
rs575865086	snp	C/T	7.37626e-05	0.00607255	synonymous-codon	RC3H2	GRCh38.p7	9:122897489	CAGAAATTCTGTCCA[C/T]TGAGCTGCCTGCACA	54542
rs575900913	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122891305	TGGAATTACAGGCGT[A/G]AGCCTCTGTGCCCAG	54542
rs575939014	snp	A/C	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122890674	TGTGCTTTCATTTTT[A/C]TAACAGTATTCTGTC	54542
rs575970315	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122856082	CCCTTTTCACTTTGT[C/T]CTTTAAGTGCTCATA	54542
rs576115493	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122904706	ACCCTCTACGCTAGG[A/G]TCTCGGGAAGCCCCA	54542
rs576127995	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122864026	ACAGGCCTGAGCCAC[C/T]GTGCCCAGCCTGTAA	54542
rs576162879	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871455	GTTGCCCACCACCAG[A/G]CCCGGCTAATTTTTT	54542
rs576164653	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122863539	TATAAAATTTTCCTG[C/T]CCTTTAATCCAACTT	54542
rs576175035	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122859648	AATTGAACATAAGCA[C/T]ACATAAATAAAACAT	54542
rs576249543	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122870878	TGTGCCTGCTACCAA[A/G]CAGCTAAATGTTGGA	54542
rs576277676	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850070	CAACCTCTGCCTCCT[A/G]GATTCAAGCAATTCT	54542
rs576298859	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893989	ATACAGGCCAGGTGC[A/G]GTGGCTCACACTTGG	54542
rs576299338	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122886236	CAGCATGTATCAGTA[C/T]TTATTCCTTTTATGG	54542
rs576318578	snp	G/T	0.0197687	0.0974348	intron-variant	RC3H2	GRCh38.p7	9:122856814	AACTTTTCTCAAGTC[G/T]AACTCAGCAGATCGG	54542
rs576338526	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122893441	TGAGGTTGCAGTGAG[A/C]TGAGATCGCACCAGT	54542
rs576346170	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880848	GCTTTCTCCCTTCAA[C/T]TGATTCGTTTATTCC	54542
rs576370712	in-del	-/AA	0.00835141	0.0640778	intron-variant	RC3H2	GRCh38.p7	9:122853163	AAGATGTGCTTTGTT[-/AA]AAACAGATGCTTGAA	54542
rs576371821	snp	C/T	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122872739	ACAGGCGTGCACCAC[C/T]ATGCCCGGCTAATTT	54542
rs576456335	snp	A/G	1.65787e-05	0.00287907	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880145	CAAACAGAAATGAGA[A/G]TGCTTTTTACTTTGG	54542
rs576536037	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122902079	GGATTACAGGCATGC[A/G]CCACCAGGCCCAGCT	54542
rs576617423	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886985	TCTATATAAAAGTAG[A/C]TTTTTAAAATATCTT	54542
rs576712696	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122873337	TGGAAATAAGAAGTA[A/C]GAACTGTATATTATT	54542
rs576773048	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881419	GCTGAGATAGCACCA[C/T]AGCACTCCAGCCTGA	54542
rs576815181	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864725	TCCTGGGTTCATGCC[A/C]TTCTCCTACCTCAGC	54542
rs576832890	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122869116	TTGCCATGTTGGCCA[G/T]GCTGGTCTCAAAATC	54542
rs576910599	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122864161	TTTTTTCCTAGCAGG[C/T]ATATAACAGATACTG	54542
rs576926733	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122857610	CTTTATGCAAATGTA[C/G]TAATACAGTGCTGGC	54542
rs576938918	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850187	ACCATGTTGGCCAGG[C/T]TGGTCTAGAACTCCT	54542
rs576956505	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122887813	GAAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	54542
rs576993725	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894419	TGGAGAGGAGAAGAG[A/G]TAGCCAATCAATAAA	54542
rs577046392	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122851922	CCCGGCCGCCACCCC[A/G]TCTGGGAAGTGAGGA	54542
rs577084260	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122894026	GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	54542
rs577146420	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122865739	AATGGGCAATGGGAA[C/T]AGATTGAAAAAGGAG	54542
rs577157100	snp	A/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122858490	TCTCACAACAGCCTT[A/T]TGAGGTAGGTACTAC	54542
rs577230953	snp	G/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122873430	AAAGATGAAGAACCC[G/T]TGCCAGGTGCCATGG	54542
rs577236554	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122850743	CGCCCAGCCTAGCCA[A/G]GAAAATCTTAACATG	54542
rs577285800	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122874121	GTTATCCAGATAAAG[A/G]GGAGAGAGAAAATAA	54542
rs577317640	snp	C/T	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122895615	TGCACCTTGATTTCA[C/T]AGTGTGTAACTTGAT	54542
rs577414870	snp	G/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122859310	ATGATGCCCAGGCTG[G/T]TCGCAAACTCCTGGG	54542
rs577466785	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122904026	TGAGTGACTTTATAC[C/T]ACTGTGGTATAGCAA	54542
rs577476080	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122862551	TTTTCCTGTGTTCCA[A/G]TAACAACTGGAACAA	54542
rs577505344	snp	A/G	0.0119091	0.0762411	intron-variant	RC3H2	GRCh38.p7	9:122866557	TTGCAGGCGCGCGCC[A/G]CCACGCCTGACTGGT	54542
rs577552086	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122869497	GACAAGTGCTCCTAG[A/G]TTAGACTGGCTAAAA	54542
rs577553136	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122903522	TTTAACAAAAATATA[C/T]GAACAAAGGACGTAA	54542
rs577576010	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122901146	CTTCTTTAACTGTCA[C/T]ATATGTATACATCAT	54542
rs577607571	snp	A/G	0.000798403	0.0199641	intron-variant	RC3H2	GRCh38.p7	9:122885311	GTCGGTAAAGAATAT[A/G]TAAAAAATTCTCTGC	54542
rs577630206	snp	A/C	0.00119737	0.0244387	intron-variant	RC3H2	GRCh38.p7	9:122876660	TGATACACTGGCCAG[A/C]AGAAAGTAGAAAAGC	54542
rs577636619	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122898075	AAGAAAACAGCTTTG[A/C]CACCTGAAAGAGGAA	54542
rs577751825	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122855956	AATATAAAGTAACTA[C/T]TATAGAATTCAGAGG	54542
rs577833976	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122861052	AGTAAATACTTGCTG[C/G]GTGAATGAAATGGTA	54542
rs577881066	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122879016	CTCACCTCAACCTCC[A/C]AAAGTGCTGGGATTA	54542
rs577918639	snp	A/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122878287	TATTTTTATCTTTGA[A/G]ACGGAGTCTTGCTCT	54542
rs577920681	snp	A/C	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122886156	CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGTGT	54542
rs577953106	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906843	CCTAGAGAACTGTTA[A/G]CAACCAATAATTGTT	54542
rs577994053	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892552	GAATAGCTGGAACTA[C/T]AGGTGCCTGCCAAGA	54542
rs578048300	snp	C/T	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122892000	GACTGAATGAATACA[C/T]GCATACATGAAGCTG	54542
rs578059889	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122899493	ACAAACTTTCTCAAA[C/G]AGCTCTAATGCAAAT	54542
rs578107202	snp	G/T	0.00398564	0.0444627	intron-variant	RC3H2	GRCh38.p7	9:122871507	TTTCACCGTGTTAGT[G/T]GGGGGGGGGGTTTCA	54542
rs578162123	snp	C/G	0.000399281	0.0141238	intron-variant	RC3H2	GRCh38.p7	9:122871017	CCACTTTCAACCACC[C/G]CTCCTACAGCTAGAT	54542
rs578241274	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122889160	AAATATTTTCCCCAG[G/T]TGGTCTTCTTTTTCA	54542
rs745363821	snp	C/T	1.67416e-05	0.00289318	missense	RC3H2	GRCh38.p7	9:122855208	TGATGGGCTTAGTCG[C/T]ACTTCCTTGGGAAGC	54542
rs745400993	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122857416	TAAATAATACTGTAG[A/G]TATTTCTGCACTTCT	54542
rs745402271	snp	A/G	1.65712e-05	0.00287843	intron-variant	RC3H2	GRCh38.p7	9:122855400	CACTGTCCAGGTCCT[A/G]TGTAAACCAAAGAAA	54542
rs745404836	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122896162	ATTTGTGTTGGGCTG[C/T]ATTCAAAGCTGTCCT	54542
rs745405430	snp	C/T	2.48908e-05	0.00352772	intron-variant	RC3H2	GRCh38.p7	9:122849871	AGCTTTAAGTGCAAA[C/T]TGTTAAGGGTGACTA	54542
rs745471352	snp	C/T	9.93723e-05	0.00704814	synonymous-codon	RC3H2	GRCh38.p7	9:122851113	ACCTAAACTCTGTTT[C/T]TTCTGCTTTGGTGGC	54542
rs745502922	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122863962	GGCTGGTCTTGAACG[C/T]CCAACCTCAGGTGAT	54542
rs745555959	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122882496	AATTTAAATGTTTTA[C/T]TTTCATAGAAGCCAA	54542
rs745627135	snp	A/T	5.2082e-05	0.00510277	intron-variant	RC3H2	GRCh38.p7	9:122865707	TTCACTAAATCTTAC[A/T]CAAGACAAAAAATGG	54542
rs745666844	snp	A/G/T	5.06251e-05	0.00503094	missense	RC3H2	GRCh38.p7	9:122858674	CTTCACTTACCCTTG[A/G/T]TAAAGGCACAGTTGT	54542
rs745679914	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122887934	ATTTTTAGTAGAGAC[A/T]GGGTTTCGCCATGTT	54542
rs745714426	in-del	-/A	1.7232e-05	0.00293525	intron-variant	RC3H2	GRCh38.p7	9:122865698	GGTGAATATTTCACT[-/A]AATCTTACTCAAGAC	54542
rs745843521	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122873582	GCCAGGCATGGTGGC[A/G]TGTGTCTGTGGTCCC	54542
rs745851657	snp	A/C	1.70974e-05	0.00292376	intron-variant	RC3H2	GRCh38.p7	9:122897262	CACCAACCTATAGTA[A/C]AATCTTGAATGCTTA	54542
rs745865422	snp	C/T	1.65605e-05	0.0028775	synonymous-codon	RC3H2	GRCh38.p7	9:122858777	TGTCTGATAGACAGA[C/T]GAGTGCATCACATCC	54542
rs745967764	snp	A/G	1.71888e-05	0.00293157	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880247	GATTCCACAGTAGGA[A/G]TATCAGTGATGAATT	54542
rs745986587	snp	A/G	8.69014e-05	0.00659114	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849611	GTGGTCACAAATTTG[A/G]AAGATGAACCTCCTT	54542
rs746127369	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122858546	GAACTGAGGCATAGG[A/G]AGGTCAAGTAACTTC	54542
rs746147720	in-del	-/ATG			intron-variant	RC3H2	GRCh38.p7	9:122884433	TATATAATTTAAAAA[-/ATG]ATATTAGCCTCTGAA	54542
rs746153702	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122888177	ATTATGAACAATATG[A/T]CAAACAAATATAATT	54542
rs746159600	snp	A/G	1.66327e-05	0.00288376	intron-variant	RC3H2	GRCh38.p7	9:122860140	AATTTTACTGGAGAG[A/G]AAATTTAACAAAGGG	54542
rs746180739	snp	A/C	1.7327e-05	0.00294333	intron-variant	RC3H2	GRCh38.p7	9:122890215	AAGATTTGTACATAT[A/C]AAGACGGGTTGAGTC	54542
rs746195505	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849060	AAAGAATGCTAGTAT[A/C]TAACCCTGTAAAATT	54542
rs746217564	in-del	-/C			intron-variant	RC3H2	GRCh38.p7	9:122875481	ATTGTCTGTGGCTGT[-/C]TTTTTTGCTACAGTG	54542
rs746241777	snp	G/T	1.65611e-05	0.00287755	missense	RC3H2	GRCh38.p7	9:122865395	CAGCATTCTGACCAT[G/T]AGCGCCAACCTTTCC	54542
rs746247604	snp	C/T	1.66073e-05	0.00288156	missense	RC3H2	GRCh38.p7	9:122851426	GCATCTTCTGTATAA[C/T]CACTCTGTAACTAAG	54542
rs746255254	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122903743	AAATTTTGAAAACAT[G/T]AATCTCCAAATCAAC	54542
rs746277135	snp	G/T	1.6563e-05	0.00287771	missense	RC3H2	GRCh38.p7	9:122857967	GAGAAGGTGGTGTTG[G/T]TGACTGTGTTGCCAC	54542
rs746290602	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122865985	AGACCATTTGAAAAT[G/T]TTGTATAACTAGAAT	54542
rs746333525	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122850636	TTTTGTAGAGACAGG[A/G]TTTCACTATGTTGGC	54542
rs746367267	snp	C/T	1.65894e-05	0.00288	missense	RC3H2	GRCh38.p7	9:122890345	ATCCTCGAGCCCTGA[C/T]AGCGGCCCATAGATT	54542
rs746412711	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122873109	TGTATAATAGAGAAA[G/T]AAAATATAGGTAAAA	54542
rs746416637	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122904866	GCGTCCGCTCGGCCA[C/G]TGTCGAAGGAAGGTG	54542
rs746450586	snp	A/G	1.65616e-05	0.00287759	synonymous-codon	RC3H2	GRCh38.p7	9:122883240	CAGTAGTTGCACAAC[A/G]TGACCAATACTTGTT	54542
rs746497757	snp	A/G	3.31246e-05	0.00406955	missense	RC3H2	GRCh38.p7	9:122851139	GTGGCTCCTTTTGGT[A/G]CTGCTGTACTGGATG	54542
rs746515596	snp	A/G	9.73947e-05	0.00697767	intron-variant	RC3H2	GRCh38.p7	9:122875149	CGATTGGGTACAAAC[A/G]GCATCTTTTTTCCTT	54542
rs746523752	snp	A/T	1.65789e-05	0.0028791	intron-variant	RC3H2	GRCh38.p7	9:122851282	ATTTTATAAATTTTC[A/T]ATCAAACAAAGCCTC	54542
rs746554104	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122903043	ATTCACAGAAGCCAC[-/A]ATTTCAAATCTTCAA	54542
rs746574750	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904971	CCGAGTGTCAGGTGC[A/G]GCCCTCAGTTCCCAA	54542
rs746658830	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849344	TGCACCGGATTGCTA[A/C]AAACTCATAAAAAGC	54542
rs746685111	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122885862	GTTTCTTTCATTTAA[C/T]GTGTTTTTTGTTTTG	54542
rs746701901	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122876203	ATTATAACACAGCAT[-/A]ATATAACAGGCTGGA	54542
rs746707331	snp	G/T	1.66073e-05	0.00288156	missense	RC3H2	GRCh38.p7	9:122858701	TTGTCCTTGGCTCAC[G/T]TGGTGGCTGACAAGC	54542
rs746722519	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907106	CACTCTGTCACACAG[A/G]CTGGAGTGCAATGGT	54542
rs746726870	snp	C/G			missense	RC3H2	GRCh38.p7	9:122865610	ACTTTATTTAGAAGA[C/G]GAAACGTTCTTACAG	54542
rs746737640	in-del	-/TATTT	1.65748e-05	0.00287874	intron-variant	RC3H2	GRCh38.p7	9:122851266	CCTTCAGTATGAAAG[-/TATTT]TATAAATTTTCAATC	54542
rs746769341	in-del	-/CATCTGTGT			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905693	GAGCAGAATCTGATA[-/CATCTGTGT]CACATTCTTCTTCAC	54542
rs746777386	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122905018	GGCGACAGCGCACAG[A/G]CCCCAGGGCTGAGAC	54542
rs746780143	snp	C/T	1.69974e-05	0.0029152	intron-variant	RC3H2	GRCh38.p7	9:122897268	CCTATAGTAAAATCT[C/T]GAATGCTTACCTGGG	54542
rs746800624	snp	G/T	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122858805	TCCATTGGAGGTAAA[G/T]AATTGCTTCTAATAA	54542
rs746801787	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122875237	AAGCATGTTTCTGCT[C/G]TTTTCACTGCACACA	54542
rs746837833	snp	A/G	1.67284e-05	0.00289205	intron-variant	RC3H2	GRCh38.p7	9:122854520	TCATATAGAATTAAG[A/G]AGAACGTTACCTTTC	54542
rs746892928	snp	A/G	1.66949e-05	0.00288915	missense	RC3H2	GRCh38.p7	9:122849652	ACCATCTTCCCATTT[A/G]CAACAGGTTTTAAAA	54542
rs746929377	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122858135	TAATCATCTAGGGAG[C/T]GGTGAATAAATTTAA	54542
rs746970230	in-del	-/TGAGAATGGAGAATCATA	0.000153527	0.00876014	intron-variant	RC3H2	GRCh38.p7	9:122854491	AGATACATACAAGTC[-/TGAGAATGGAGAATCATA]TGAGAATGGAGAATC	54542
rs747020595	in-del	-/AAAA	0.000233628	0.0108055	intron-variant	RC3H2	GRCh38.p7	9:122893030	ATGATCTGGTACCTT[-/AAAA]AAAAAAAAAAAGGAA	54542
rs747037073	snp	A/C	1.66568e-05	0.00288585	intron-variant	RC3H2	GRCh38.p7	9:122860158	ATTTAACAAAGGGCA[A/C]AGGAGAAATCACTGT	54542
rs747037563	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122856247	ATATCCTAAAGGAGT[A/T]TATAATTTTCTTTTT	54542
rs747045540	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122861964	GAAAATGATTAGGAT[G/T]TCCTTAAAACAATAA	54542
rs747050497	snp	A/G	4.99039e-05	0.00499495	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880354	TGAGGTCAGAATATA[A/G]ATAAATTTGAGACTT	54542
rs747088439	snp	C/T	1.66103e-05	0.00288182	missense	RC3H2	GRCh38.p7	9:122849749	TGATGGGGAGGCAAC[C/T]TGCATTGCTAATAGA	54542
rs747092304	snp	C/T	3.31214e-05	0.00406935	missense	RC3H2	GRCh38.p7	9:122865422	TTCCCACTTTCTTCA[C/T]GGTCTCCAGAGCTCT	54542
rs747100752	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122860478	ACTGACATAATCACA[A/G]TAACAGCTCACTGCA	54542
rs747133492	in-del	-/TTT			intron-variant	RC3H2	GRCh38.p7	9:122891022	GCCCCATTTTTTTTT[-/TTT]TTTTTTTTTTTTGGA	54542
rs747170054	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122901428	GCTAGAAACTCAGTA[C/T]TGGAGAAAAAGGAAT	54542
rs747186425	in-del	-/CAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870397	AAACAAACAAACAAA[-/CAAACAAAC]AAACAAACAAAAAAA	54542
rs747291077	snp	C/T	1.65677e-05	0.00287812	synonymous-codon	RC3H2	GRCh38.p7	9:122890373	ATTGGCAGACAACTG[C/T]TGAGGGTTCTGGTGC	54542
rs747294248	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122893030	ATGATCTGGTACCTT[-/A]AAAAAAAAAAAAAAG	54542
rs747300657	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122900238	CCTTTAAGATATAAA[A/G]GTAAAACACTGCCAA	54542
rs747305533	snp	C/G	8.52595e-05	0.00652859	intron-variant	RC3H2	GRCh38.p7	9:122890559	ACCTTTAGGAAAAGG[C/G]AAACAAAGGGAGCTA	54542
rs747308581	snp	A/T	1.65723e-05	0.00287852	intron-variant, missense	RC3H2	GRCh38.p7	9:122853921	AAAACAAATACATTA[A/T]GCATGAAGCCGAAAG	54542
rs747311647	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122872363	AAACTCCCACCTGTG[C/G]ACCAATATAGAAGTT	54542
rs747394596	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122850728	AGCCATGAGCCACTA[C/T]GCCCAGCCTAGCCAA	54542
rs747424281	snp	A/G	3.31285e-05	0.00406978	missense	RC3H2	GRCh38.p7	9:122854037	TTCCACTTCTGTTGC[A/G]TGGCCAAAGCATTGG	54542
rs747504103	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122879134	GGCACGATGGCTCAC[G/T]CCTGTAATCCCAGCA	54542
rs747505387	in-del	-/G	4.99963e-05	0.00499956	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879904	AAGGGCATGGGGGTT[-/G]GGGGGGAAGAATGTT	54542
rs747547732	snp	A/G	2.46418e-05	0.00351003	intron-variant	RC3H2	GRCh38.p7	9:122890290	TAGCTAATAAAAAAG[A/G]TAAGATAGTAACCTA	54542
rs747561637	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122871795	ACAATGTAAGCCCCC[A/G]GAGGACAAGACTTTT	54542
rs747577731	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122898639	CTGTAATTCCAGCTA[C/G]TAGGGAGGCTGAGGC	54542
rs747589293	snp	C/T			missense	RC3H2	GRCh38.p7	9:122892954	GTGCCAAATCCTCAA[C/T]GCATTTCTTTGCAAC	54542
rs747615728	snp	A/T	0.000138036	0.00830655	intron-variant	RC3H2	GRCh38.p7	9:122875388	GTAAGATAGACAAAC[A/T]TTTAATAAACAGATC	54542
rs747619924	snp	A/G	1.7315e-05	0.00294231	synonymous-codon	RC3H2	GRCh38.p7	9:122859059	AAAGCGAGGAACACA[A/G]GGAGCCACACCAGCT	54542
rs747624966	snp	A/C	1.65875e-05	0.00287984	missense	RC3H2	GRCh38.p7	9:122851413	TTTAGTATCTGTTGC[A/C]TCTTCTGTATAATCA	54542
rs747642435	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122851018	CCAAAAATTAATTTC[A/G]CATTTTTTTCTCTTT	54542
rs747664704	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904648	GCCCTCCCAGGGCAT[C/T]GTTTGGCCGGGGTTC	54542
rs747665366	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886674	CAACCTGAGCAATGG[A/G]GCAAGACCCTGTCTC	54542
rs747668785	snp	C/T	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122858821	AATTGCTTCTAATAA[C/T]GTCATCTCGTTGGTA	54542
rs747686718	snp	A/G	1.65666e-05	0.00287802	synonymous-codon	RC3H2	GRCh38.p7	9:122877572	AGTCTTGTATTTGCT[A/G]TTTGGCTGAGGCTAC	54542
rs747694266	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122893275	AAGCCAGCAGATTAA[C/T]TTAAGTTAGGAGTTT	54542
rs747695392	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122870412	CAAACAAACAAACAA[A/C]CAAAAAAAAAACAAC	54542
rs747843023	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122852757	CGTCCGGGAGGGAGG[C/T]GGGGGGGTCAGCCCC	54542
rs747851296	snp	A/G	2.19894e-05	0.00331575	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897521	GCATTGTGGAAGCTG[A/G]ATGCTCGGGTTAGCA	54542
rs747869335	snp	A/G	1.77168e-05	0.00297626	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880288	CTCAGAATCTGCCCT[A/G]TGAAATTCATCATTA	54542
rs747901733	in-del	-/G			intron-variant	RC3H2	GRCh38.p7	9:122904200	AAAAAAAGGAAGGCC[-/G]TGGGTAAGGGGAGAG	54542
rs747951304	snp	A/G	1.67276e-05	0.00289197	intron-variant	RC3H2	GRCh38.p7	9:122854639	ATGTAGAATGAAACA[A/G]TGGTCAAAAAAGTGA	54542
rs747955735	snp	A/G	1.68678e-05	0.00290407	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880551	CTAATACTCTTCAAT[A/G]TAACAGCAATGATAG	54542
rs747976928	snp	A/G	2.756e-05	0.00371204	intron-variant	RC3H2	GRCh38.p7	9:122849853	TGACATTAAAAACAA[A/G]TTAGCTTTAAGTGCA	54542
rs748068049	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122885974	CTCACTGCAACCTCC[A/G]CCTCCTAGGTTCAAA	54542
rs748096110	in-del	-/TCTG	0.000165653	0.00909941	intron-variant	RC3H2	GRCh38.p7	9:122851065	ACTGTTTATGAATTT[-/TCTG]TCTAACACTCACAGA	54542
rs748105387	snp	G/T	3.31214e-05	0.00406935	missense	RC3H2	GRCh38.p7	9:122865448	GCTCTTAAGGTACTG[G/T]CAGTACTACGTGAGA	54542
rs748120134	in-del	-/A	0.001722	0.0292922	intron-variant	RC3H2	GRCh38.p7	9:122855884	CTCTGAGAACTGGTT[-/A]AAAAAAAAATAAATA	54542
rs748125414	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122884839	CCTGGCGACATAGCG[-/A]AAAGTCCGTCTCCAA	54542
rs748156797	snp	C/G	8.28123e-05	0.00643423	missense	RC3H2	GRCh38.p7	9:122858000	GAAGAGTTGAAGAGA[C/G]AAGAGGTGCTTTCTG	54542
rs748213376	snp	C/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882267	ATTTCAATTGTTGCC[C/G]TAAGAGCATGAAACT	54542
rs748241416	snp	A/C	0.00014906	0.00863178	missense	RC3H2	GRCh38.p7	9:122865566	AAATGACATTTCCGG[A/C]TGTGGTTGTGACAGT	54542
rs748271527	snp	C/T	1.65652e-05	0.0028779	intron-variant, synonymous-codon	RC3H2	GRCh38.p7	9:122853946	CGAAAGGTTCAGTTT[C/T]TTTACCTCTCCATTT	54542
rs748294500	snp	C/T	1.66067e-05	0.00288151	missense	RC3H2	GRCh38.p7	9:122858093	AATGACCACAAGGTT[C/T]CTAATGGGGGATAAA	54542
rs748371776	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122889999	ATAGAAAAATTAGCC[A/G]GGTATGATGGCGTGT	54542
rs748378694	snp	C/G	1.75742e-05	0.00296425	intron-variant	RC3H2	GRCh38.p7	9:122890572	GGGAAACAAAGGGAG[C/G]TAAAGTTTTTTCAAT	54542
rs748381692	snp	A/T	3.31713e-05	0.00407242	missense	RC3H2	GRCh38.p7	9:122892979	TGCAACCTCATAGTG[A/T]TTATTCTCACCTAGA	54542
rs748389507	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122869030	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	54542
rs748400110	snp	C/T	3.32491e-05	0.00407719	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879919	GGGGGGGAAGAATGT[C/T]AGCAGTAATTCTCTT	54542
rs748410121	in-del	-/C			intron-variant	RC3H2	GRCh38.p7	9:122898564	GAACAGCCTGACCAA[-/C]CATGGATAAACCCTG	54542
rs748439839	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903374	TTTTTTTAGCGTTCT[C/T]AGCTATTGCAAACAA	54542
rs748488787	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122863925	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	54542
rs748519894	snp	G/T	9.94365e-05	0.00705042	intron-variant	RC3H2	GRCh38.p7	9:122859900	TTTTTTTCTTAGAAT[G/T]GTCTAAAATTACTCA	54542
rs748548355	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122896313	CCTTATTGTTTCATT[C/T]ACACTATTATATAAA	54542
rs748580573	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122894305	AATAATTATATTTAT[A/G]GAGTGCTTACCATGC	54542
rs748644929	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122862199	TCAAAAATTGGAACT[C/T]ATAGAAAAAGCTAAT	54542
rs748665283	in-del	-/C			intron-variant	RC3H2	GRCh38.p7	9:122870389	CCAAAAACAAACAAA[-/C]AAACAAACAAACAAA	54542
rs748716263	snp	A/C	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122859990	CTGAATGTTTTCAGA[A/C]TGCGGAGGATATACT	54542
rs748726976	in-del	-/TTC			intron-variant	RC3H2	GRCh38.p7	9:122901203	AACCTTAGGGCTTAG[-/TTC]TTCTAATTAAAACCA	54542
rs748748873	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122855979	TTCAGAGGACTTCAT[A/G]GCAAACAATTATACT	54542
rs748755902	snp	A/C	1.65614e-05	0.00287757	synonymous-codon	RC3H2	GRCh38.p7	9:122858939	AGGAGGAGGCTGGTA[A/C]GGAGAAGAATTCATT	54542
rs748781480	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122870096	AAAATAAAACTTGGC[C/T]GGGCATGGTGGCTCA	54542
rs748801879	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122873485	TGGGAGGCTGAGGTG[C/G]GCAGATTGAGCTCAG	54542
rs748808197	snp	C/T	1.66574e-05	0.0028859	intron-variant	RC3H2	GRCh38.p7	9:122854627	TAATCTACAGACATG[C/T]AGAATGAAACAATGG	54542
rs748935895	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122895819	TTGTAAAATGGGGAT[A/C]ATAACTACCTGAAAA	54542
rs748937861	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881207	AGAAAGGTGAGGAGG[C/T]CAGGGATGGTGGCTC	54542
rs749002477	snp	C/T	1.66438e-05	0.00288472	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880581	GAACATCAGCATCTC[C/T]AATTTCACAAACCTT	54542
rs749016956	in-del	-/CAAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870401	AAACAAACAAACAAA[-/CAAACAAACAAAC]AAAAAAAAAACAACA	54542
rs749018631	snp	C/T	1.67077e-05	0.00289026	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880787	GAGTCTTCATCTCTT[C/T]TGGTAACCTAAAAAA	54542
rs749053119	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884444	AAAAATGATATTAGC[C/T]TCTGAATGCAAAACC	54542
rs749075477	snp	A/C	6.64916e-05	0.00576553	intron-variant	RC3H2	GRCh38.p7	9:122849858	TTAAAAACAAATTAG[A/C]TTTAAGTGCAAACTG	54542
rs749091485	snp	C/G	3.31268e-05	0.00406968	missense	RC3H2	GRCh38.p7	9:122865585	GGTTGTGACAGTGTT[C/G]TTTACACCAACTTTA	54542
rs749114826	snp	C/T	3.31246e-05	0.00406955	missense	RC3H2	GRCh38.p7	9:122851108	TCTTCACCTAAACTC[C/T]GTTTCTTCTGCTTTG	54542
rs749218032	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122871984	GGTCTTGCTATGTTG[C/T]CCAGGCTGGTCACAA	54542
rs749233897	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886811	TGCTTGTTAGTCATC[A/G]TGTCTCTTCTTTGGA	54542
rs749310623	snp	C/T	1.65971e-05	0.00288067	missense	RC3H2	GRCh38.p7	9:122892990	AGTGTTTATTCTCAC[C/T]TAGATTACTTAACTT	54542
rs749384018	snp	A/G			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849048	ATATAATGCAGTAAA[A/G]AATGCTAGTATATAA	54542
rs749402869	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122863517	TTTCCCATATTTCTC[C/T]CAGCAATATAAAATT	54542
rs749412338	snp	C/T	3.33422e-05	0.00408289	missense	RC3H2	GRCh38.p7	9:122854217	TCAAAAGGTCCCCAG[C/T]ACTGGAATGCTTTCT	54542
rs749500239	in-del	-/G	9.71157e-05	0.00696767	intron-variant	RC3H2	GRCh38.p7	9:122855134	AAAAAAAAAAAAAAA[-/G]GGCATAGTGCTTAGA	54542
rs749508216	snp	C/T	3.31757e-05	0.00407269	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879964	AAAAGTAGAAAAAAA[C/T]ATAAGCAACTGAGCA	54542
rs749513389	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857715	GGAAAGATTTTGAAT[C/T]CTTAGTAAAGGACTA	54542
rs749520318	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122876793	TAGGTCTCGGGTAAA[A/G]GGACATAGAAAAAGG	54542
rs749542627	in-del	-/CTCTCC	0.0300682	0.11887	intron-variant	RC3H2	GRCh38.p7	9:122851457	AAAATACTGATTTTG[-/CTCTCC]CTCTCCCTCTCCCTC	54542
rs749543551	snp	C/T	1.65822e-05	0.00287938	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880108	GACACTCTTTGCAAA[C/T]GACTCTGGAGACTGT	54542
rs749562076	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122859997	TTTTCAGAATGCGGA[A/G]GATATACTGGTACTC	54542
rs749604666	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122870241	TTAGCCAGAAGTGGT[A/G]GGACATGCCTGTAAT	54542
rs749654692	snp	C/T	1.66588e-05	0.00288602	missense	RC3H2	GRCh38.p7	9:122855829	GACCAGGGAGAATAA[C/T]GGGAAAGATGATCTT	54542
rs749661637	snp	C/G	1.96442e-05	0.00313396	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849594	GTAAATGCTTCCATG[C/G]TGTGGTCACAAATTT	54542
rs749675932	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882223	AGTTTTACAGGGCCT[A/G]GTGAGGTTGTGTGTG	54542
rs749733651	snp	C/T	1.65622e-05	0.00287764	synonymous-codon	RC3H2	GRCh38.p7	9:122883315	AAGTACCAGAACTTT[C/T]CTTGAGAGGGCAGAA	54542
rs749742578	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903620	TGAACACGAGTGTAA[C/T]TAAATCCTCATAGAA	54542
rs749811932	in-del	-/AGG			intron-variant	RC3H2	GRCh38.p7	9:122890048	TTAGGGGGCTGAGTC[-/AGG]AGAATTGCTTGAGCA	54542
rs749852172	snp	C/G	1.65699e-05	0.00287831	intron-variant	RC3H2	GRCh38.p7	9:122851306	AAGCCTCTCAATTAT[C/G]TAATTGTGGCACTTA	54542
rs749868771	snp	G/T	1.79396e-05	0.00299491	intron-variant	RC3H2	GRCh38.p7	9:122890205	TAATTATATCAAGAT[G/T]TGTACATATAAAGAC	54542
rs749911250	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122886639	AGTTACAGTGGGCTA[-/T]TAAGCGTGCCACTGC	54542
rs749920004	snp	C/T	0.000132679	0.00814382	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880062	AGTTAGCTGGGTCAC[C/T]TGTTCGTTGCAAAAC	54542
rs749936573	snp	A/G	1.68021e-05	0.0028984	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880213	ATCAACATATTTAAT[A/G]CGTTTTCAAGTGTCT	54542
rs749943392	in-del	-/TCTC			intron-variant	RC3H2	GRCh38.p7	9:122871823	TTTGCCTTTCTTGCA[-/TCTC]TCTATCTTTAGCACA	54542
rs749947513	snp	A/G/T	3.35989e-05	0.0040986	intron-variant	RC3H2	GRCh38.p7	9:122854276	CTGTCCCTTTAAAGA[A/G/T]AAATATGTTTATTGT	54542
rs749988232	snp	C/T	1.65619e-05	0.00287762	synonymous-codon	RC3H2	GRCh38.p7	9:122860074	TCCAACATTAGAGGG[C/T]CCAGCTGAGGTAGCT	54542
rs750034261	snp	C/T	3.31923e-05	0.0040737	missense	RC3H2	GRCh38.p7	9:122855793	TCAATGGCATTTATA[C/T]AGGAGCCTATGGTGC	54542
rs750076818	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122898375	GAATAAAACATTATT[C/T]TAAAAAGTTATATAT	54542
rs750126798	snp	A/C	3.41396e-05	0.00413142	intron-variant	RC3H2	GRCh38.p7	9:122883402	TATTAAAGGAACATG[A/C]GTTCATGACAAATGA	54542
rs750183914	snp	C/T	4.0032e-05	0.00447375	intron-variant	RC3H2	GRCh38.p7	9:122855908	ATAAATAAAGCCAAT[C/T]AGTAAGAAGCTTAAA	54542
rs750190017	snp	C/G	0.000361816	0.0134453	intron-variant	RC3H2	GRCh38.p7	9:122875308	CTCATTATGTACAGT[C/G]CCCAAGCTAGCCACT	54542
rs750239985	snp	A/C	3.314e-05	0.00407049	intron-variant	RC3H2	GRCh38.p7	9:122851251	AAATAAAATGTTAAT[A/C]CTTCAGTATGAAAGT	54542
rs750261114	snp	C/T	0.000103093	0.00717884	intron-variant	RC3H2	GRCh38.p7	9:122890262	TCCAGAAATTGGCAT[C/T]CTCAAGCCCCAATAG	54542
rs750270656	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122903225	TTCATGAGACTGGAT[A/G]CAAAACATGAACTTA	54542
rs750293131	snp	C/T	1.65737e-05	0.00287864	missense	RC3H2	GRCh38.p7	9:122851391	CTAACTCGATATCCC[C/T]ATCAGGTTTAGTATC	54542
rs750346532	snp	A/G	6.03676e-05	0.00549365	intron-variant	RC3H2	GRCh38.p7	9:122851487	CTCCCTCTCCCCATG[A/G]TCTCCCTCTCCCCAT	54542
rs750373449	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122875012	TCTGACTTTTTTAGT[C/T]GAACTTTCTCAAAAG	54542
rs750377192	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122890861	TGTAAGAATATTGCT[C/T]CAGCAATTCTCCCCT	54542
rs750399870	in-del	-/A	3.31702e-05	0.00407235	intron-variant	RC3H2	GRCh38.p7	9:122892885	GTCCTACTTATCAGT[-/A]AAAAATGCATTTTAT	54542
rs750432073	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904194	GAAATGAAAAAAAGG[A/G]AGGCCGTGGGTAAGG	54542
rs750432275	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122889701	CTTTGGCTTATTACG[G/T]GTTCAATCTTAGGCC	54542
rs750434628	snp	C/G	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122877510	GCAAATGTACAATTT[C/G]TTCCTCGTGGACAAC	54542
rs750452906	snp	A/G	1.69553e-05	0.00291159	synonymous-codon	RC3H2	GRCh38.p7	9:122897453	ATTCTCATCAAATTC[A/G]TTATAGCAGATTGGA	54542
rs750464714	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122854967	TAAAAATACAAAAAT[C/T]AGCCAGGCATGGTGG	54542
rs750471890	snp	G/T	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858897	CATTCCAGAAGGTAC[G/T]GGAGGAACTGGTCCA	54542
rs750483336	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122894308	AATTATATTTATGGA[A/G]TGCTTACCATGCACT	54542
rs750493831	snp	G/T	3.51401e-05	0.00419152	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897559	AGATCATTATTTTGC[G/T]GTGTAGTGTTTTGTA	54542
rs750527318	snp	A/G	9.94646e-05	0.00705141	synonymous-codon	RC3H2	GRCh38.p7	9:122858987	TGTACTGTAATGATC[A/G]GCATATGGCATGGAA	54542
rs750527462	snp	A/G	1.6593e-05	0.00288031	synonymous-codon	RC3H2	GRCh38.p7	9:122854608	AGCATTGACATAAGG[A/G]ACATAATCTACAGAC	54542
rs750547197	snp	A/G	3.32005e-05	0.00407421	synonymous-codon	RC3H2	GRCh38.p7	9:122849735	ACTGACAGATGTGGT[A/G]ATGGGGAGGCAACTT	54542
rs750582190	snp	A/G	9.41398e-05	0.0068601	intron-variant	RC3H2	GRCh38.p7	9:122855152	CATAGTGCTTAGAAC[A/G]TATCAGGCTAGGTAT	54542
rs750635710	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895318	GACTACAGTCACACA[C/T]CACCATGCCTGACTA	54542
rs750701459	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122886359	TGAATAACGCTGCAA[G/T]AAACATTTGTATACA	54542
rs750714442	snp	C/G	2.25421e-05	0.00335716	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880340	CTGTATTAACTCTCT[C/G]AGGTCAGAATATAGA	54542
rs750754380	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899215	TCAAGTGATTCTCCC[A/G]CCTTGGCCTCCCAAG	54542
rs750767072	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906356	GCCAACATAGTGAAA[C/T]CCTGGCTCTACTAAA	54542
rs750804201	snp	A/G	4.96833e-05	0.00498389	synonymous-codon, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880690	GAGTCCTGCTTCCAT[A/G]GCAATATGAACAATT	54542
rs750806868	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122874927	GTTTGAAGGTATGAG[A/G]AAGAAGAAAATGGAT	54542
rs750849295	snp	A/G	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122865511	ATTCCGTTTGTACTT[A/G]GAACAATTTTCCCTG	54542
rs750932734	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122871295	TACCTGCTCAAATGT[C/T]GTATCTTCTTTTTTT	54542
rs751015028	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122861570	GGATTTGTAGCTATA[C/T]TTATTTTGCTGATTG	54542
rs751044112	snp	C/T	1.65658e-05	0.00287795	missense	RC3H2	GRCh38.p7	9:122860085	AGGGCCCAGCTGAGG[C/T]AGCTGCTACATTACT	54542
rs751097347	snp	A/G	1.66529e-05	0.00288551	synonymous-codon	RC3H2	GRCh38.p7	9:122865354	TAATACCTACTTTTC[A/G]GTTACAGAATCTGCA	54542
rs751124106	in-del	-/T	1.77811e-05	0.00298165	intron-variant	RC3H2	GRCh38.p7	9:122890577	CAAAGGGAGCTAAAG[-/T]TTTTTTCAATAAAAA	54542
rs751150696	snp	G/T	1.65707e-05	0.00287838	missense	RC3H2	GRCh38.p7	9:122857952	CTACACTGAACAGAG[G/T]AGAAGGTGGTGTTGG	54542
rs751160575	in-del	-/CAAACA			intron-variant	RC3H2	GRCh38.p7	9:122870405	AAACAAACAAACAAA[-/CAAACA]AACAAAAAAAAAACA	54542
rs751165305	snp	C/T	1.65787e-05	0.00287907	synonymous-codon	RC3H2	GRCh38.p7	9:122851407	ATCAGGTTTAGTATC[C/T]GTTGCATCTTCTGTA	54542
rs751225211	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865726	GACAAAAAATGGCAA[C/T]GGGCAATGGGAATAG	54542
rs751265132	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899476	GTAAAAAGCACCCCT[A/G]TACAAACTTTCTCAA	54542
rs751293223	snp	C/T	3.42847e-05	0.00414019	intron-variant	RC3H2	GRCh38.p7	9:122890278	CTCAAGCCCCAATAG[C/T]TAATAAAAAAGGTAA	54542
rs751298059	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122862427	CCTGTGCTGCCTTCT[C/T]CATCCACAAGGCCCT	54542
rs751307123	snp	C/T	7.227e-05	0.00601081	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853861	CATCAGAGATAGGCA[C/T]ACCAAAATGCACTCA	54542
rs751346053	snp	C/T	0.000331159	0.0128635	synonymous-codon	RC3H2	GRCh38.p7	9:122858915	AGGAACTGGTCCATA[C/T]GGCTGCGGAGGAGGA	54542
rs751346542	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122876738	AAAACAAAACAACAA[A/T]AATTGGATAATAGTA	54542
rs751378087	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905496	TCTGCCTCAGCGGAT[C/T]CACCCCGATCACGTG	54542
rs751409573	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122891236	CCATGTTGGCCAGGG[C/T]GGTCTCAAATTCCTG	54542
rs751467418	in-del	-/AAGAGTTGA	1.66644e-05	0.00288651	intron-variant	RC3H2	GRCh38.p7	9:122860161	AACAAAGGGCAAAGG[-/AAGAGTTGA]AGAAATCACTGTCTA	54542
rs751470098	in-del	-/TAGG			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881933	AAGGAATCCAGCTAA[-/TAGG]TAGGCATATATTACC	54542
rs751620005	snp	A/C/T	3.3127e-05	0.00406972	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880733	TCTCTGCGTAATGCT[A/C/T]CATAACTCCGAAATT	54542
rs751660635	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895366	AGAGATGGGGTTTCG[C/T]CATGTTGTCCAGGCT	54542
rs751753869	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122863439	TCTAAAAGACTGGTC[A/T]CCTCAATATTCCATA	54542
rs751753964	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122882738	TGGGCCAATCTCCTC[A/C]ACTTTCCATTTCCTG	54542
rs751756338	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122877028	CTCAAAATATGACCA[A/C]TGAGTAAAGTTCTAA	54542
rs751854697	snp	C/T	1.65737e-05	0.00287864	intron-variant	RC3H2	GRCh38.p7	9:122883164	AGGAAGTCTCTGTCT[C/T]ACAAACAGGCATGTC	54542
rs751886370	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122887343	GCCCCACTTACATCT[A/C]GTAGGAGCTCCTTCA	54542
rs751890191	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122865557	CTATGACAGAAATGA[C/T]ATTTCCGGCTGTGGT	54542
rs751903253	in-del	-/TCTACAAA			intron-variant	RC3H2	GRCh38.p7	9:122900268	AATTTTGGCAATAAC[-/TCTACAAA]TCTACCAAATTTTCT	54542
rs751963239	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122871639	AATGTTGTATCTTCT[A/G]AGAGTCTTTCCTACA	54542
rs751998148	snp	C/T	1.78522e-05	0.0029876	intron-variant	RC3H2	GRCh38.p7	9:122858633	CTCCAGACACTGGGC[C/T]GTTAATGACTACATT	54542
rs752045832	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906988	TATACATACATATAA[A/G]TATATATACACATAT	54542
rs752155444	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122887514	TTCCTACCCTAGACT[A/G]GAGTAAGGCATTTAC	54542
rs752217691	in-del	-/AA	1.65835e-05	0.00287949	intron-variant	RC3H2	GRCh38.p7	9:122854109	AGGAGGGAAAAAAAG[-/AA]AAGTTAGCTTCCAAC	54542
rs752224654	snp	C/T	4.97096e-05	0.00498521	missense	RC3H2	GRCh38.p7	9:122858063	TTCTTATCTGCTCCT[C/T]GCAACTGGTCTTCAA	54542
rs752250852	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122868899	TGTGTGTATGTGTTT[-/TT]TTTTTTTTTTTTTGT	54542
rs752276054	snp	C/G	1.65649e-05	0.00287788	missense	RC3H2	GRCh38.p7	9:122853999	AAAGGTTTAAGGTAA[C/G]GTGACGGCCTTCATC	54542
rs752279194	snp	C/G	1.65842e-05	0.00287955	missense	RC3H2	GRCh38.p7	9:122890510	GTTTCCTTTGCATTG[C/G]ACGGCTCAGTGCACT	54542
rs752314559	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122873244	TTTTTTAAACTGAAA[A/G]GACAGTCACATCACC	54542
rs752336095	snp	A/G	1.65864e-05	0.00287974	intron-variant	RC3H2	GRCh38.p7	9:122892884	AAGTCCTACTTATCA[A/G]TAAAAATGCATTTTA	54542
rs752406222	in-del	-/CTTA	4.67694e-05	0.00483555	intron-variant	RC3H2	GRCh38.p7	9:122859136	AATATTTAATGTAAT[-/CTTA]CTTAGTACAATCCAA	54542
rs752448338	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122878325	AGGCTGGAGTGCAGT[G/T]GCGCCATCTCAGCTC	54542
rs752474268	in-del	-/AA			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881458	GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	54542
rs752499085	snp	C/T	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122859952	ACTTCAAAGGGTATC[C/T]GAGTCCTTGGATCTT	54542
rs752515615	snp	C/T	1.68007e-05	0.00289828	missense	RC3H2	GRCh38.p7	9:122859028	GGGAGGACTCTGGAA[C/T]GTTATTGGACCTCAC	54542
rs752529785	snp	A/G	1.6607e-05	0.00288153	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879883	CAGCGTCTAAAATAA[A/G]CCACCAAGGGCATGG	54542
rs752568541	snp	A/G	3.16932e-05	0.00398065	intron-variant	RC3H2	GRCh38.p7	9:122859120	TGAAAATTGGAAAGA[A/G]GAATATTTAATGTAA	54542
rs752621317	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899659	ACTGAGCAGATGAAT[A/G]TATCACTCCCTAAAA	54542
rs752622707	snp	C/T	4.96857e-05	0.00498401	synonymous-codon	RC3H2	GRCh38.p7	9:122855332	AATTATTGGATCTTC[C/T]TCTTTTGTCCTTCTC	54542
rs752652300	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122861662	ATCTTGTTAATTATG[C/G]AGGAACTCAATACAT	54542
rs752668168	snp	A/C	1.65641e-05	0.00287781	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880737	TGCGTAATGCTTCAT[A/C]ACTCCGAAATTCCTC	54542
rs752719581	snp	C/T	1.65701e-05	0.00287833	intron-variant	RC3H2	GRCh38.p7	9:122883179	CACAAACAGGCATGT[C/T]TTTACATAGATACTT	54542
rs752720361	snp	A/C/T	6.81261e-05	0.00583602	intron-variant	RC3H2	GRCh38.p7	9:122865681	AAAACAATCAACAGA[A/C/T]TGGTGAATATTTCAC	54542
rs752765180	snp	A/C	1.65636e-05	0.00287776	missense	RC3H2	GRCh38.p7	9:122851185	CATTCCATTTAGCAA[A/C]TGATCATTTTGAGAA	54542
rs752845050	in-del	-/AAA	0.000347319	0.0131734	intron-variant	RC3H2	GRCh38.p7	9:122893030	ATGATCTGGTACCTT[-/AAA]AAAAAAAAAAAAGGA	54542
rs752845286	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122902710	TACAAAAATTAGCCT[A/G]GTGTAGTGGTGCCTT	54542
rs752853169	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904402	TTCTCCCATCCTGAA[A/G]GCTAAGGATAGAAAA	54542
rs752918520	snp	A/G	1.76965e-05	0.00297454	intron-variant	RC3H2	GRCh38.p7	9:122858644	GGGCTGTTAATGACT[A/G]CATTATAGTAGCATC	54542
rs753019153	snp	A/G	0.000109571	0.00740091	intron-variant	RC3H2	GRCh38.p7	9:122875219	GAAAAAAACTGAGAA[A/G]AGAAGCATGTTTCTG	54542
rs753031317	snp	A/G	1.65963e-05	0.0028806	synonymous-codon	RC3H2	GRCh38.p7	9:122897405	GGTCTTGCAAACAGT[A/G]TGTGAACAACCTAAA	54542
rs753045755	snp	A/G	1.79903e-05	0.00299914	intron-variant	RC3H2	GRCh38.p7	9:122893078	ATTCATCCAGCTCAT[A/G]CAACTATTATTTATG	54542
rs753070488	snp	C/T	1.65638e-05	0.00287778	missense	RC3H2	GRCh38.p7	9:122858745	CCATCTAATGAGTTA[C/T]ATCTTTCCCGCAAAG	54542
rs753079445	snp	A/T	1.66275e-05	0.00288331	missense	RC3H2	GRCh38.p7	9:122854189	ACAGAGCCTACCTGC[A/T]GAAGTTCAAGGCTCA	54542
rs753082471	in-del	-/AAACTGTTTC			intron-variant	RC3H2	GRCh38.p7	9:122900055	CTACTACACAGTTTT[-/AAACTGTTTC]AAACTATACCAGAGC	54542
rs753119160	in-del	-/AGTA			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853585	GTGAAACCCTGTCTC[-/AGTA]TACTAAAAACACAAA	54542
rs753133750	snp	C/G/T	6.63387e-05	0.00575896	synonymous-codon, missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880084	TTGCAAAACAATTGT[C/G/T]AATTCCTGGACACTC	54542
rs753143428	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882010	AGGAGGATGGCCTAC[A/G]CCCAGGAGTTCAAGG	54542
rs753162645	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122855538	TAATCCAACAAACTA[C/T]CAGTAAACCACCAAT	54542
rs753188549	snp	A/T	1.69146e-05	0.0029081	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880219	ATATTTAATACGTTT[A/T]CAAGTGTCTTCAGAT	54542
rs753196843	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122895526	CTAAAATGTTGTTTG[A/C]AAGAGGCAACATTTT	54542
rs753286564	snp	A/G	1.65647e-05	0.00287786	missense	RC3H2	GRCh38.p7	9:122854005	TTAAGGTAAGGTGAC[A/G]GCCTTCATCCAGGGA	54542
rs753289530	snp	G/T	1.65704e-05	0.00287836	missense	RC3H2	GRCh38.p7	9:122892929	CCTCCACTTAGTGGT[G/T]TTAAGTAGAGTGCCA	54542
rs753307682	snp	A/T			utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849622	TTTGAAAGATGAACC[A/T]CCTTTCAGCTGTTAA	54542
rs753350620	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122859535	TTGCCACTGGTTTTG[G/T]ATTAGTCAGTTATAT	54542
rs753385217	snp	A/C/T	5.37479e-05	0.00518378	intron-variant	RC3H2	GRCh38.p7	9:122858626	GGTTTGACTCCAGAC[A/C/T]CTGGGCTGTTAATGA	54542
rs753457911	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122857334	ACCAGATTAAATTAA[A/G]ATCATCCTGGTACAC	54542
rs753482688	snp	C/G	1.65861e-05	0.00287972	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880040	AAATGAGGCCTCAGT[C/G]TATTTAAGTTAGCTG	54542
rs753491304	in-del	-/ATTT			intron-variant	RC3H2	GRCh38.p7	9:122873128	ATATAGGTAAAATTA[-/ATTT]ATTTAAGTTGAACAA	54542
rs753510418	in-del	-/ATT	1.68508e-05	0.0029026	intron-variant, cds-indel	RC3H2	GRCh38.p7	9:122853882	ATGCACTCAGTAATG[-/ATT]GTATAACCAAGATGC	54542
rs753543930	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122867298	GGGGGTCAGCCCCCC[A/G]CCCGGCCAGCCGCCC	54542
rs753546317	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122859955	TCAAAGGGTATCTGA[A/G]TCCTTGGATCTTGAA	54542
rs753584423	snp	A/G	1.66048e-05	0.00288134	intron-variant	RC3H2	GRCh38.p7	9:122859868	TTCATTCATTTATCT[A/G]AAGGAAACAATGTTT	54542
rs753631568	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122863004	AGTATATTCACAAGG[C/T]TGTCCAATTATCACC	54542
rs753652622	snp	A/G	1.65622e-05	0.00287764	synonymous-codon	RC3H2	GRCh38.p7	9:122855350	TTTTGTCCTTCTCTG[A/G]GTTTCAAATAAATGT	54542
rs753677652	snp	G/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881727	TGCAGTGGCACAATC[G/T]AGGCTCGCTGTAGCC	54542
rs753709937	snp	A/C	1.6582e-05	0.00287936	synonymous-codon	RC3H2	GRCh38.p7	9:122855741	TCATACCATTAACAC[A/C]GCATTTGAATTAGCA	54542
rs753799385	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122887849	CCGAGGTTAGGGCAA[G/T]TCTCGTGCCTCAGCT	54542
rs753820122	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899853	TCATAATGGCCACCT[A/G]TTTGGAAATGTTAAT	54542
rs753824017	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122871109	CGCTACCAATTCCAG[C/T]AACCTTCCTGCACCT	54542
rs753856274	snp	C/T	1.70536e-05	0.00292002	intron-variant	RC3H2	GRCh38.p7	9:122883398	AAAATATTAAAGGAA[C/T]ATGAGTTCATGACAA	54542
rs753885984	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122871367	CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC	54542
rs753892401	snp	C/T	0.000115427	0.00759606	intron-variant	RC3H2	GRCh38.p7	9:122875281	TCTATCACAATGCTG[C/T]TGCTTGTAGAGCTCA	54542
rs753893611	snp	C/G/T	0.000463641	0.0152188	missense	RC3H2	GRCh38.p7	9:122858754	GAGTTATATCTTTCC[C/G/T]GCAAAGATGTCTGAT	54542
rs753915704	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122850428	ACTATATTATATGCT[A/G]TCTATCTATAGATAG	54542
rs753945334	snp	C/G	1.7105e-05	0.00292441	intron-variant	RC3H2	GRCh38.p7	9:122854486	CCCTTAAGATACATA[C/G]AAGTCTGAGAATGGA	54542
rs753950295	snp	C/T	1.65671e-05	0.00287807	synonymous-codon	RC3H2	GRCh38.p7	9:122877485	CTTTTCAAGCTCTTC[C/T]TGAGAATGGGCAAAT	54542
rs753950450	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904697	GCCTCCACCACCCTC[C/T]ACGCTAGGGTCTCGG	54542
rs753965342	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122869950	TATATTTCAGGAAGA[C/T]AATCTGGTTGTCTGG	54542
rs753986266	snp	C/G			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853733	CTCCAGGCGATAGAG[C/G]AAGATTCCATCTCAA	54542
rs754000071	snp	A/G	3.31203e-05	0.00406928	synonymous-codon	RC3H2	GRCh38.p7	9:122858876	GCTGTCGTACACAGG[A/G]GCATACATTCCAGAA	54542
rs754002917	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892660	TTGTGATCCGCCCGC[A/G]CTGGCCTCCCAAAGT	54542
rs754108637	snp	G/T			splice-acceptor-variant	RC3H2	GRCh38.p7	9:122851438	TAATCACTCTGTAAC[G/T]AAGAAAAATACTGAT	54542
rs754110176	snp	C/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905580	CGAAGGGATTGATGG[C/G]AAATTCCCTGCACAT	54542
rs754176128	snp	C/G/T	6.84409e-05	0.00584948	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880242	CTTCAGATTCCACAG[C/G/T]AGGAGTATCAGTGAT	54542
rs754197738	snp	A/C	2.90263e-05	0.0038095	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897544	GGTTAGCAGTCTAGC[A/C]GATCATTATTTTGCT	54542
rs754207726	snp	A/G	1.74995e-05	0.00295795	intron-variant	RC3H2	GRCh38.p7	9:122883428	AATGAGGAACCCATC[A/G]GATCATGTGTGTCAT	54542
rs754216932	in-del	-/CAA			intron-variant	RC3H2	GRCh38.p7	9:122870409	AAACAAACAAACAAA[-/CAA]ACAAAAAAAAAACAA	54542
rs754231413	snp	A/G	1.66172e-05	0.00288242	synonymous-codon	RC3H2	GRCh38.p7	9:122860131	TGGAGAACCAATTTT[A/G]CTGGAGAGAAAATTT	54542
rs754262475	snp	A/C	1.70947e-05	0.00292354	synonymous-codon	RC3H2	GRCh38.p7	9:122849801	GCAAGAAGTTACCGG[A/C]AGAATTGTTTTTTGC	54542
rs754274505	snp	C/G	1.65982e-05	0.00288077	missense	RC3H2	GRCh38.p7	9:122849710	GAGTTTTCAGAATGA[C/G]GTTGCCAGCACTGAC	54542
rs754280906	snp	C/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880434	GCATCCCTTTATTTT[C/G]CAAGTAGAAAAATAA	54542
rs754391802	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884919	GGAATATCAGTGTCA[C/T]GAAAGGCAAAGAAAA	54542
rs754436013	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122877377	AGCCCTTAACTTGCA[A/T]TTTTGAAAGTCATCA	54542
rs754455866	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122899477	TAAAAAGCACCCCTA[C/T]ACAAACTTTCTCAAA	54542
rs754484730	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122885930	TCTTGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT	54542
rs754516183	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122871689	TCCCCTTTCTCAATC[A/T]CTCTTTTTCTCCTTT	54542
rs754531527	in-del	-/AT			intron-variant	RC3H2	GRCh38.p7	9:122903857	TAAGAAAGGCATGTG[-/AT]AAGCTACAACAGTGG	54542
rs754571398	snp	A/G	1.65792e-05	0.00287912	missense	RC3H2	GRCh38.p7	9:122851408	TCAGGTTTAGTATCT[A/G]TTGCATCTTCTGTAT	54542
rs754636693	in-del	-/T	1.68244e-05	0.00290033	intron-variant, frameshift-variant	RC3H2	GRCh38.p7	9:122853883	TGCACTCAGTAATGG[-/T]TATAACCAAGATGCA	54542
rs754648906	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886618	CACTTGAAGCCAGAA[A/G]TTCCGAAGTTACAGT	54542
rs754670099	snp	A/C	3.20703e-05	0.00400426	intron-variant	RC3H2	GRCh38.p7	9:122890280	CAAGCCCCAATAGCT[A/C]ATAAAAAAGGTAAGA	54542
rs754693014	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122887742	TTTTATACTTGTATC[-/T]TTTTTTTTTTTTTTT	54542
rs754698951	snp	C/T	1.72829e-05	0.00293959	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853871	AGGCACACCAAAATG[C/T]ACTCAGTAATGGTAT	54542
rs754704417	snp	C/T	1.6563e-05	0.00287771	missense	RC3H2	GRCh38.p7	9:122877549	TGTCGCAAATCTCGG[C/T]ACATGCTAGTCTTGT	54542
rs754737951	snp	A/G	0.000149033	0.00863099	missense	RC3H2	GRCh38.p7	9:122858916	GGAACTGGTCCATAC[A/G]GCTGCGGAGGAGGAG	54542
rs754762878	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122887136	AGCCACAAATAATTC[A/T]TGCTGAAGCCCATTA	54542
rs754776059	snp	A/T	3.49321e-05	0.00417909	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879734	GACAACAGCAGTCAG[A/T]AATGTAATAAATGTA	54542
rs754863552	snp	A/C/G	0.000566674	0.0168238	missense	RC3H2	GRCh38.p7	9:122859019	CAGGTGGGAGGGAGG[A/C/G]CTCTGGAACGTTATT	54542
rs754873975	snp	A/G	2.5434e-05	0.003566	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880359	TCAGAATATAGATAA[A/G]TTTGAGACTTTGTAA	54542
rs754918689	snp	C/T	2.11365e-05	0.00325082	intron-variant	RC3H2	GRCh38.p7	9:122855168	TATCAGGCTAGGTAT[C/T]ATCTAAATGGATTAC	54542
rs754931139	snp	C/T	1.66852e-05	0.0028883	intron-variant	RC3H2	GRCh38.p7	9:122854632	TACAGACATGTAGAA[C/T]GAAACAATGGTCAAA	54542
rs755030714	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122877801	CTTCTGAAGATTATT[C/T]GAAACTGGTTCAAAT	54542
rs755031882	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881933	AAGGAATCCAGCTAA[C/T]AGGTAGGCATATATT	54542
rs755064250	snp	A/G	1.65658e-05	0.00287795	intron-variant	RC3H2	GRCh38.p7	9:122851068	GTTTATGAATTTTCT[A/G]TCTAACACTCACAGA	54542
rs755087409	in-del	-/CAATA			intron-variant	RC3H2	GRCh38.p7	9:122898273	ATATCTTGTATTGTT[-/CAATA]CAATACTTCTGATAA	54542
rs755198388	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903283	ACCCATGCTTCCTTT[C/T]TCCATCACTAAAAAG	54542
rs755208127	snp	A/G	1.69295e-05	0.00290937	intron-variant	RC3H2	GRCh38.p7	9:122865672	CCTGTTTCAAAAACA[A/G]TCAACAGATTGGTGA	54542
rs755227245	snp	C/T	3.31257e-05	0.00406962	missense	RC3H2	GRCh38.p7	9:122865563	CAGAAATGACATTTC[C/T]GGCTGTGGTTGTGAC	54542
rs755245506	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122898843	ACTTCCCAGAATTTC[-/T]TTTATCTTCCAATTC	54542
rs755256455	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122863516	ATTTCCCATATTTCT[C/G]CCAGCAATATAAAAT	54542
rs755304570	snp	A/C/G	3.31847e-05	0.00407326	synonymous-codon	RC3H2	GRCh38.p7	9:122858088	CTTCAAATGACCACA[A/C/G]GGTTCCTAATGGGGG	54542
rs755346971	snp	C/G	1.65792e-05	0.00287912	missense	RC3H2	GRCh38.p7	9:122892970	GCATTTCTTTGCAAC[C/G]TCATAGTGTTTATTC	54542
rs755355708	snp	C/T	1.65658e-05	0.00287795	missense	RC3H2	GRCh38.p7	9:122854049	TGCATGGCCAAAGCA[C/T]TGGCCTCTCTCTGAA	54542
rs755364317	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907054	TACACATTATATATA[C/T]ATATATGTACATATT	54542
rs755408855	snp	A/C/G	8.3098e-05	0.00644541	intron-variant	RC3H2	GRCh38.p7	9:122854180	AGCTGAGTTACAGAG[A/C/G]CTACCTGCTGAAGTT	54542
rs755412756	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122854340	GTAATAACCATATGT[G/T]TTATGTGACAGATCA	54542
rs755434263	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880560	TTCAATGTAACAGCA[A/G]TGATAGAACATCAGC	54542
rs755466622	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880855	CCCTTCAACTGATTC[A/G]TTTATTCCTTTTTCA	54542
rs755470873	snp	G/T	1.66161e-05	0.00288232	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879909	CATGGGGGTTGGGGG[G/T]GAAGAATGTTAGCAG	54542
rs755487340	snp	C/T	1.65877e-05	0.00287986	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880067	GCTGGGTCACCTGTT[C/T]GTTGCAAAACAATTG	54542
rs755500950	snp	C/T	1.78688e-05	0.00298899	intron-variant	RC3H2	GRCh38.p7	9:122893069	CAGAAATACATTCAT[C/T]CAGCTCATGCAACTA	54542
rs755503292	snp	A/T	1.65811e-05	0.00287929	intron-variant	RC3H2	GRCh38.p7	9:122859893	ATGTTTCTTTTTTTC[A/T]TAGAATTGTCTAAAA	54542
rs755504404	in-del	-/AAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870386	TCTCCAAAAACAAAC[-/AAACAAAC]AAACAAACAAACAAA	54542
rs755520461	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122894160	GTTACTCCAGAGGCT[G/T]AGGCAGGAGAATGCC	54542
rs755545283	snp	C/T			synonymous-codon	RC3H2	GRCh38.p7	9:122855359	TCTCTGGGTTTCAAA[C/T]AAATGTACTCTTCTC	54542
rs755574101	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122857755	GGTCTTCAGAGTCTC[A/G]TAACACCTAGCCGTA	54542
rs755578891	snp	A/T	1.66891e-05	0.00288864	intron-variant, missense	RC3H2	GRCh38.p7	9:122853891	AGTAATGGTATAACC[A/T]AGATGCAGCAGCAGA	54542
rs755597250	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122871798	ATGTAAGCCCCCGGA[A/G]GACAAGACTTTTGCC	54542
rs755632050	snp	G/T	8.28205e-05	0.00643455	missense	RC3H2	GRCh38.p7	9:122854000	AAGGTTTAAGGTAAG[G/T]TGACGGCCTTCATCC	54542
rs755633003	snp	A/G	1.66421e-05	0.00288458	synonymous-codon	RC3H2	GRCh38.p7	9:122890534	GTGCACTCTGGTTCA[A/G]GCTAGCTACACCTTT	54542
rs755720768	snp	C/T	1.71387e-05	0.00292729	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879755	AATAAATGTACTTAC[C/T]TGAGGGGTCTCATGG	54542
rs755737939	snp	A/G	3.3151e-05	0.00407117	intron-variant	RC3H2	GRCh38.p7	9:122877598	GCTACAAAAATGGGA[A/G]CACATTCAATGAGTG	54542
rs755750938	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884247	GCAGTGAGCCGAGAT[C/T]GTGCCACCACACTCC	54542
rs755806352	snp	C/G	1.6609e-05	0.0028817	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879891	AAAATAAGCCACCAA[C/G]GGCATGGGGGTTGGG	54542
rs755866840	snp	C/T	2.04484e-05	0.00319747	intron-variant	RC3H2	GRCh38.p7	9:122855170	TCAGGCTAGGTATTA[C/T]CTAAATGGATTACCT	54542
rs755904102	snp	A/G	3.22648e-05	0.00401639	intron-variant	RC3H2	GRCh38.p7	9:122859121	GAAAATTGGAAAGAG[A/G]AATATTTAATGTAAT	54542
rs755953814	in-del	-/C	1.73474e-05	0.00294506	intron-variant	RC3H2	GRCh38.p7	9:122865706	TTTCACTAAATCTTA[-/C]TCAAGACAAAAAATG	54542
rs755990961	in-del	-/TTTTT			intron-variant	RC3H2	GRCh38.p7	9:122868896	GTGTGTGTGTATGTG[-/TTTTT]TTTTTTTTTTTTTGT	54542
rs755993944	snp	C/T			synonymous-codon	RC3H2	GRCh38.p7	9:122859975	TGGATCTTGAAAATA[C/T]TGAATGTTTTCAGAA	54542
rs756020015	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122899849	TTTTTCATAATGGCC[A/G]CCTGTTTGGAAATGT	54542
rs756032352	snp	A/G	1.6563e-05	0.00287771	missense	RC3H2	GRCh38.p7	9:122865568	ATGACATTTCCGGCT[A/G]TGGTTGTGACAGTGT	54542
rs756042350	snp	G/T	1.65636e-05	0.00287776	missense	RC3H2	GRCh38.p7	9:122851095	CAGAATCACATGGTC[G/T]TCACCTAAACTCTGT	54542
rs756107187	snp	C/T	1.65619e-05	0.00287762	missense	RC3H2	GRCh38.p7	9:122855337	TTGGATCTTCTTCTT[C/T]TGTCCTTCTCTGGGT	54542
rs756167812	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865190	GTTGCAGAACCAAAC[C/T]AGAACTCAAATTTTT	54542
rs756203316	in-del	-/CCCCGTCCGGGAGGGAGGTGGGGGGATCAGCCCCCCGCCCGGCCAGCCG			intron-variant	RC3H2	GRCh38.p7	9:122867213	TCCGCCCGGCAGCCA[lengthTooLong]CCCCGTCCGGGAGGG	54542
rs756292144	snp	G/T	3.77629e-05	0.00434512	intron-variant	RC3H2	GRCh38.p7	9:122897234	ATAATGGCAAAAATA[G/T]TGATTATTTTTGCAC	54542
rs756308544	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122890011	GCCGGGTATGATGGC[A/G]TGTGCCTGTAGTCCC	54542
rs756313343	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122850392	TTATTCAAAATGGCA[C/G]TATTATAGCCAAGAA	54542
rs756313574	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122894768	ACCTGCAACCCCAGC[C/T]ACTTGGGAGGCTGAG	54542
rs756322470	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122891283	CCGCCTCGGCCTCTC[A/C]AAGTGCTGGAATTAC	54542
rs756339280	snp	G/T	1.6563e-05	0.00287771	missense	RC3H2	GRCh38.p7	9:122858747	ATCTAATGAGTTATA[G/T]CTTTCCCGCAAAGAT	54542
rs756342744	snp	C/T	3.31746e-05	0.00407262	missense	RC3H2	GRCh38.p7	9:122892983	ACCTCATAGTGTTTA[C/T]TCTCACCTAGATTAC	54542
rs756375819	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904535	AGGGAAAGAAGAAAG[C/T]CATAGCAGAATTTCC	54542
rs756446857	in-del	-/TTTTTTTTTTTT			intron-variant	RC3H2	GRCh38.p7	9:122891013	ACCAAATCTGCCCCA[-/TTTTTTTTTTTT]TTTTTTTTTTTTGGA	54542
rs756524938	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122857226	AAAGATTTTAAAAAT[G/T]TTAATATCAGAACTT	54542
rs756553599	snp	A/T	1.65957e-05	0.00288055	missense	RC3H2	GRCh38.p7	9:122897406	GTCTTGCAAACAGTG[A/T]GTGAACAACCTAAAC	54542
rs756554874	in-del	-/GTTTTA	1.66726e-05	0.00288722	cds-indel	RC3H2	GRCh38.p7	9:122849659	TCCCATTTGCAACAG[-/GTTTTA]AAAAGTCGTTTTTAT	54542
rs756557176	snp	C/T	0.000103889	0.00720649	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849586	AAGCTAGTGTAAATG[C/T]TTCCATGGTGTGGTC	54542
rs756632087	snp	A/G	0.000115979	0.00761422	synonymous-codon	RC3H2	GRCh38.p7	9:122860095	TGAGGTAGCTGCTAC[A/G]TTACTTACAGGAGTC	54542
rs756643815	snp	C/G	1.692e-05	0.00290856	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880223	TTAATACGTTTTCAA[C/G]TGTCTTCAGATTCCA	54542
rs756743079	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122896849	CCAACATAGTGAAAC[C/G]CCGTCTCTACTAAAA	54542
rs756855269	in-del	-/CAAACAAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870397	AAACAAACAAACAAA[-/CAAACAAACAAACAAAC]AAAAAAAAAACAACA	54542
rs756856112	snp	A/G	1.66023e-05	0.00288113	intron-variant	RC3H2	GRCh38.p7	9:122859871	ATTCATTTATCTAAA[A/G]GAAACAATGTTTCTT	54542
rs756983745	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122859962	GTATCTGAGTCCTTG[A/G]ATCTTGAAAATACTG	54542
rs756986074	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895895	AAACCTAATGCAAAG[C/T]AGACCCTCATTAAAT	54542
rs756990106	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122869562	GCCAGTTTACACGAT[-/TT]TTTTTTTTTTTTTTT	54542
rs757005812	in-del	-/AT	1.69358e-05	0.00290992	intron-variant	RC3H2	GRCh38.p7	9:122854507	TGAGAATGGAGAATC[-/AT]ATAGAATTAAGAAGA	54542
rs757021176	snp	A/G	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122855357	CTTCTCTGGGTTTCA[A/G]ATAAATGTACTCTTC	54542
rs757027572	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122863042	CTGAAACATTTTCAT[C/T]ATCCCCAAGAGAAAC	54542
rs757079771	snp	C/G	1.6582e-05	0.00287936	missense	RC3H2	GRCh38.p7	9:122855742	CATACCATTAACACA[C/G]CATTTGAATTAGCAA	54542
rs757081739	snp	C/T	0.000115931	0.00761264	synonymous-codon	RC3H2	GRCh38.p7	9:122851110	TTCACCTAAACTCTG[C/T]TTCTTCTGCTTTGGT	54542
rs757089360	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122849840	GAGAAAAAAGAAATG[A/G]CATTAAAAACAAATT	54542
rs757112493	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122901295	GTACTTCCCCGTTTA[A/G]AAAACTTAAAAATAA	54542
rs757127051	snp	C/G	3.3129e-05	0.00406982	intron-variant	RC3H2	GRCh38.p7	9:122883196	TTACATAGATACTTA[C/G]TGCTTACCTTAAAAC	54542
rs757134735	snp	A/G	1.65674e-05	0.00287809	intron-variant	RC3H2	GRCh38.p7	9:122851242	CTCCTAAGAAAATAA[A/G]ATGTTAATCCTTCAG	54542
rs757137977	snp	A/G	1.70458e-05	0.00291935	intron-variant	RC3H2	GRCh38.p7	9:122883399	AAATATTAAAGGAAC[A/G]TGAGTTCATGACAAA	54542
rs757153048	snp	C/T	1.71293e-05	0.00292649	intron-variant	RC3H2	GRCh38.p7	9:122865692	CAGATTGGTGAATAT[C/T]TCACTAAATCTTACT	54542
rs757154560	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122887854	GTTAGGGCAATTCTC[A/G]TGCCTCAGCTTCGCG	54542
rs757178138	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889385	TTGTAATTTATATAG[C/T]TTATAGAGAATAAGA	54542
rs757208139	snp	A/T	1.72555e-05	0.00293725	intron-variant	RC3H2	GRCh38.p7	9:122858661	ATTATAGTAGCATCT[A/T]CACTTACCCTTGGTA	54542
rs757219079	in-del	-/AAA			intron-variant	RC3H2	GRCh38.p7	9:122890220	TGTACATATAAAGAC[-/AAA]GGGTTGAGTCTCAGG	54542
rs757230508	in-del	-/TCTTAA	1.65608e-05	0.00287752	cds-indel	RC3H2	GRCh38.p7	9:122865434	CACGGTCTCCAGAGC[-/TCTTAA]TCTTAAGGTACTGTC	54542
rs757254668	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122891331	CCCAGCCTCTGTTCC[A/G]TTTCTTTCTTCTCTT	54542
rs757433820	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878383	GCCATTCTCCCTGCC[C/T]CAGAGAGCTCCCAAG	54542
rs757463932	snp	C/T	3.31752e-05	0.00407265	missense	RC3H2	GRCh38.p7	9:122854601	AATCAACAGCATTGA[C/T]ATAAGGGACATAATC	54542
rs757470472	in-del	-/ATT			intron-variant	RC3H2	GRCh38.p7	9:122871874	CATCCCAAGTGCCCA[-/ATT]ATTATTATTATTATT	54542
rs757485094	snp	A/G	1.70714e-05	0.00292154	intron-variant	RC3H2	GRCh38.p7	9:122854489	TTAAGATACATACAA[A/G]TCTGAGAATGGAGAA	54542
rs757504896	snp	A/G	1.66255e-05	0.00288314	intron-variant	RC3H2	GRCh38.p7	9:122860135	GAACCAATTTTACTG[A/G]AGAGAAAATTTAACA	54542
rs757518656	snp	G/T	1.65979e-05	0.00288074	missense	RC3H2	GRCh38.p7	9:122849711	AGTTTTCAGAATGAG[G/T]TTGCCAGCACTGACA	54542
rs757664418	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122883445	ATCATGTGTGTCATA[A/G]GCATCTTTGGGTATT	54542
rs757674033	in-del	-/CT			intron-variant	RC3H2	GRCh38.p7	9:122872458	TCCATTTAAATAAAA[-/CT]CTCTAAAATGACTTC	54542
rs757724959	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122900932	TCGCTCAAATAATTT[C/T]CCAGACTGTAAGTTC	54542
rs757763132	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906993	ATACATATAAATATA[C/T]ATACACATATATAGA	54542
rs757775949	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122865388	GGCCCAGCAGCATTC[C/T]GACCATTAGCGCCAA	54542
rs757795873	in-del	-/T	3.3184e-05	0.00407319	intron-variant	RC3H2	GRCh38.p7	9:122859884	AGGAAACAATGTTTC[-/T]TTTTTTTCTTAGAAT	54542
rs757805106	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122902415	TCTGGAAGTTTTGGG[-/TT]TTTATACATCTACTT	54542
rs757816562	snp	A/C	2.24813e-05	0.00335263	intron-variant	RC3H2	GRCh38.p7	9:122890293	CTAATAAAAAAGGTA[A/C]GATAGTAACCTATCT	54542
rs757830712	snp	A/G	1.6563e-05	0.00287771	missense	RC3H2	GRCh38.p7	9:122857963	AGAGGAGAAGGTGGT[A/G]TTGGTGACTGTGTTG	54542
rs757928955	in-del	-/T	1.65919e-05	0.00288022	intron-variant	RC3H2	GRCh38.p7	9:122854149	TCAACTGTCATTCTA[-/T]TTCTCAAAAATTTAT	54542
rs757975426	in-del	-/CT			intron-variant	RC3H2	GRCh38.p7	9:122904599	ACCCCTGTGCAACCA[-/CT]CAGGTCCGGCCGTCC	54542
rs758030193	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906817	CTTCTCTTTATGAAA[C/T]ATATGCCAGGCCTAG	54542
rs758074184	snp	C/T	1.71138e-05	0.00292516	intron-variant	RC3H2	GRCh38.p7	9:122883406	AAAGGAACATGAGTT[C/T]ATGACAAATGAGGAA	54542
rs758112961	snp	C/G	2.06286e-05	0.00321152	intron-variant	RC3H2	GRCh38.p7	9:122855914	AAAGCCAATTAGTAA[C/G]AAGCTTAAATTTACA	54542
rs758155880	snp	A/G	0.000120547	0.00776267	intron-variant	RC3H2	GRCh38.p7	9:122875313	TATGTACAGTGCCCA[A/G]GCTAGCCACTGAGGA	54542
rs758166003	snp	A/G	1.65767e-05	0.00287891	synonymous-codon	RC3H2	GRCh38.p7	9:122851401	ATCCCTATCAGGTTT[A/G]GTATCTGTTGCATCT	54542
rs758232557	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889842	ATAAATTAAGATTAA[C/T]AAAAACGGATTTATA	54542
rs758265863	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122877511	CAAATGTACAATTTG[C/T]TCCTCGTGGACAACC	54542
rs758300478	snp	C/T	3.39616e-05	0.00412064	missense	RC3H2	GRCh38.p7	9:122897457	TCATCAAATTCATTA[C/T]AGCAGATTGGACAGG	54542
rs758317050	snp	C/T	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122858905	AAGGTACTGGAGGAA[C/T]TGGTCCATACGGCTG	54542
rs758326135	in-del	-/AAG			intron-variant	RC3H2	GRCh38.p7	9:122874170	ATATAGACAAGTGAA[-/AAG]AAGAGTAAAAGAAAT	54542
rs758328046	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122858778	GTCTGATAGACAGAT[A/G]AGTGCATCACATCCA	54542
rs758329247	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122875117	CTTGATGTGAAATTC[A/T]GTATATAGAACTAGT	54542
rs758437067	snp	A/G	1.66095e-05	0.00288175	synonymous-codon	RC3H2	GRCh38.p7	9:122854614	GACATAAGGGACATA[A/G]TCTACAGACATGTAG	54542
rs758464152	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122890957	ATGCTGTTATTTCAT[C/T]CATCTAAAATACAAA	54542
rs758490150	snp	C/T	0.000118168	0.00768572	intron-variant	RC3H2	GRCh38.p7	9:122855155	AGTGCTTAGAACATA[C/T]CAGGCTAGGTATTAT	54542
rs758503571	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122872195	GAGACCACTAAGTTA[C/T]GCAGGCTCCATACCT	54542
rs758514175	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122874371	GAAAAGACAGATTGA[C/G]ATATAGGAAGATACT	54542
rs758520180	snp	C/T	1.6601e-05	0.00288101	missense	RC3H2	GRCh38.p7	9:122849737	TGACAGATGTGGTGA[C/T]GGGGAGGCAACTTGC	54542
rs758582340	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122861892	TAAGGGTTTAGAGTA[A/T]AAAGATATTTTAGGA	54542
rs758600062	snp	C/T	1.72053e-05	0.00293298	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880248	ATTCCACAGTAGGAG[C/T]ATCAGTGATGAATTA	54542
rs758625636	snp	A/G	1.65622e-05	0.00287764	synonymous-codon	RC3H2	GRCh38.p7	9:122857983	TGACTGTGTTGCCAC[A/G]GGAAGAGTTGAAGAG	54542
rs758687194	snp	C/G	1.84705e-05	0.0030389	intron-variant	RC3H2	GRCh38.p7	9:122849827	TTTGCTCCTCCCTGA[C/G]AAAAAAGAAATGACA	54542
rs758687981	snp	A/G	0.000118283	0.00768944	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880347	AACTCTCTGAGGTCA[A/G]AATATAGATAAATTT	54542
rs758718291	snp	C/G	3.31208e-05	0.00406931	missense	RC3H2	GRCh38.p7	9:122865404	GACCATTAGCGCCAA[C/G]CTTTCCCACTTTCTT	54542
rs758751410	in-del	-/AA			intron-variant	RC3H2	GRCh38.p7	9:122893030	ATGATCTGGTACCTT[-/AA]AAAAAAAAAAAAAGG	54542
rs758764058	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122886418	TCTTTTGGGTATATA[C/T]CTAGGAATAAAACTG	54542
rs758769838	snp	C/T	3.31235e-05	0.00406948	missense	RC3H2	GRCh38.p7	9:122865539	CTGTTGTTTCAGTAC[C/T]TCCTATGACAGAAAT	54542
rs758778699	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906902	TAATTTACATGTACA[C/T]ATTTGTTTTCCACCC	54542
rs758808115	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122898609	ACAAAATTAGCCAGA[C/T]GTGGTGGCACATGCC	54542
rs758816522	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122870077	CCTTGCTTTCCATCC[A/T]CAAAAAATAAAACTT	54542
rs758851135	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122892824	CTCCTTTTCCATAAC[A/T]TAATAGGGTATCCAC	54542
rs758895721	snp	A/G	0.000218189	0.0104425	intron-variant	RC3H2	GRCh38.p7	9:122890550	GCTAGCTACACCTTT[A/G]GGAAAAGGGAAACAA	54542
rs758912150	snp	C/T	1.65707e-05	0.00287838	missense	RC3H2	GRCh38.p7	9:122892935	CTTAGTGGTTTTAAG[C/T]AGAGTGCCAAATCCT	54542
rs758930995	snp	A/T	1.658e-05	0.00287919	missense	RC3H2	GRCh38.p7	9:122858080	CAACTGGTCTTCAAA[A/T]GACCACAAGGTTCCT	54542
rs758947572	snp	C/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905736	CTGTGATGACATGCC[C/G]ACAGGATCCCTCAAT	54542
rs758949568	snp	C/T	4.99405e-05	0.00499677	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879781	CATGGCCTTTTCTAC[C/T]ATAATTTTGTATGAA	54542
rs758988223	snp	C/G	1.65644e-05	0.00287783	missense	RC3H2	GRCh38.p7	9:122854007	AAGGTAAGGTGACGG[C/G]CTTCATCCAGGGAAT	54542
rs759044646	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122850647	CAGGGTTTCACTATG[C/T]TGGCCAGGCTGCTCT	54542
rs759047776	snp	A/C/T	3.31467e-05	0.00407093	synonymous-codon, missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880609	CTTATCAATGATAGA[A/C/T]TGCATGTGTGATTTA	54542
rs759075630	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122893323	CATGGTGAAACTCCA[C/T]CTCTACTAAAAACTA	54542
rs759091509	snp	C/T	1.7033e-05	0.00291826	synonymous-codon	RC3H2	GRCh38.p7	9:122849798	AAAGCAAGAAGTTAC[C/T]GGCAGAATTGTTTTT	54542
rs759124924	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122887471	TTATAAGCTTTTTTG[A/C]TTCCCTGCTCCCCGC	54542
rs759146649	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122861585	TTTATTTTGCTGATT[G/T]TATTTGCTTGTTTTA	54542
rs759148760	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881535	CAAGTGGTGAAACAG[A/G]AACATGAAAAAGCAG	54542
rs759211658	snp	G/T	3.31235e-05	0.00406948	synonymous-codon	RC3H2	GRCh38.p7	9:122865498	TTCTGCATTTGAAAT[G/T]CCGTTTGTACTTGGA	54542
rs759223953	in-del	-/G	3.57038e-05	0.004225	intron-variant	RC3H2	GRCh38.p7	9:122858633	TCCAGACACTGGGCT[-/G]GTTAATGACTACATT	54542
rs759225154	snp	A/T	1.65658e-05	0.00287795	synonymous-codon	RC3H2	GRCh38.p7	9:122858052	ATCTGGCTTTCTTCT[A/T]ATCTGCTCCTCGCAA	54542
rs759243287	in-del	-/AG			intron-variant	RC3H2	GRCh38.p7	9:122886079	ATTTTCAGTAGAGAC[-/AG]AGTTTTCCCATGTTG	54542
rs759272482	snp	C/T	3.31389e-05	0.00407042	synonymous-codon	RC3H2	GRCh38.p7	9:122890487	TTGACAGTTTACAAG[C/T]GTCACCAGTTTCCTT	54542
rs759276041	snp	C/G	1.68975e-05	0.00290662	intron-variant	RC3H2	GRCh38.p7	9:122858134	TTAATCATCTAGGGA[C/G]TGGTGAATAAATTTA	54542
rs759311047	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122862561	TTCCAATAACAACTG[C/G]AACAACTGTGTTCCA	54542
rs759359846	snp	C/G			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853526	GGAAGGTGAGGCGAG[C/G]AGATCACTTGAGGTC	54542
rs759490374	snp	C/T	1.65608e-05	0.00287752	synonymous-codon	RC3H2	GRCh38.p7	9:122859933	TGTCTGTGGGTACTG[C/T]GGGACTTCAAAGGGT	54542
rs759495711	in-del	-/AAAT			intron-variant	RC3H2	GRCh38.p7	9:122868745	TGATCAATAAAAAAT[-/AAAT]AAATAAATAAATAAA	54542
rs759500490	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122902492	CAGTAATATCCGATA[G/T]AAATATGTGAGCCAT	54542
rs759517976	snp	A/G	1.66048e-05	0.00288134	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879872	AGTTGGTGAAACAGC[A/G]TCTAAAATAAGCCAC	54542
rs759543409	snp	C/T	1.67133e-05	0.00289074	intron-variant	RC3H2	GRCh38.p7	9:122855708	CTCTCACCTCCAACC[C/T]CTGCAACCCCAGCAA	54542
rs759599346	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122873942	CCCGCCTCAGCCTCC[C/G]GAGCAGCTGGGATTA	54542
rs759607608	snp	C/T	3.31697e-05	0.00407231	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880012	ATTAGGGTCTATGTT[C/T]GCAAGAAGCTCTAAA	54542
rs759643077	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122896809	GGGCGGATCACCTGA[C/T]GTCAGGAGCTCCAGA	54542
rs759643228	snp	C/G	1.65729e-05	0.00287857	intron-variant	RC3H2	GRCh38.p7	9:122883173	CTGTCTCACAAACAG[C/G]CATGTCTTTACATAG	54542
rs759663499	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122857733	TAGTAAAGGACTATG[A/C]CTTAACGGTCTTCAG	54542
rs759759476	in-del	-/T	2.76637e-05	0.00371901	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880368	AGATAAATTTGAGAC[-/T]TTGTAAGCCTCACTG	54542
rs759822117	snp	C/T	1.65677e-05	0.00287812	synonymous-codon	RC3H2	GRCh38.p7	9:122883342	AGAACCATCTTCTAA[C/T]GCCAGTAACACCAGC	54542
rs759873654	snp	C/T	0.000109272	0.0073908	intron-variant	RC3H2	GRCh38.p7	9:122875196	CTTCTCTAGGCACTT[C/T]AAGTGGGGAAAAAAA	54542
rs759943961	snp	A/G	1.66732e-05	0.00288727	intron-variant	RC3H2	GRCh38.p7	9:122877435	CCATAAAAATCAAAA[A/G]TTAAACCCATATGAA	54542
rs759947812	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122857079	TTACTTCAAAACAAT[C/G]CAGGGGGAAGAGGGG	54542
rs759970472	snp	A/G	3.31411e-05	0.00407056	missense	RC3H2	GRCh38.p7	9:122897377	AAGCTTTTCGATGAA[A/G]TTTATTCAAGCAGGT	54542
rs759986545	snp	C/T	1.65685e-05	0.00287819	intron-variant	RC3H2	GRCh38.p7	9:122883182	AAACAGGCATGTCTT[C/T]ACATAGATACTTACT	54542
rs759999346	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122874469	TAATTTTGCCATTAT[G/T]ATTATTTTTGAATGA	54542
rs760073746	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122875692	AAGGATGAGCTAGAC[A/G]AAGGAAAGGTCTCAA	54542
rs760132524	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122863053	CATCATCCCCAAGAG[-/A]AAACCTGTACCCATT	54542
rs760137992	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122864235	ATGAATATTAAAATA[C/T]TCATCAATCTAAATC	54542
rs760145112	in-del	-/AACAAACAAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870395	ACAAACAAACAAACA[-/AACAAACAAACAAACAAAC]AAAAAAAAAACAACA	54542
rs760156090	snp	A/G	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858840	ATCTCGTTGGTACAT[A/G]GGTGGGCGCCAGATG	54542
rs760192490	snp	A/G	6.63383e-05	0.00575888	synonymous-codon	RC3H2	GRCh38.p7	9:122865627	AAACGTTCTTACAGT[A/G]GCATTGATCTTTTTG	54542
rs760202234	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889826	AAGCACTGTCTATCA[C/T]ATAAATTAAGATTAA	54542
rs760202987	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904450	TGGGAAACAAAGATG[C/T]TTTCTACCATTCTTC	54542
rs760247629	snp	C/G/T	7.18551e-05	0.00599359	intron-variant	RC3H2	GRCh38.p7	9:122858620	CTGGGTGGTTTGACT[C/G/T]CAGACACTGGGCTGT	54542
rs760253266	snp	A/C/G	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122890453	GCATGGCTCTTACAC[A/C/G]ACCTTCTTCCTCCAC	54542
rs760260671	snp	C/G	3.32508e-05	0.00407729	missense	RC3H2	GRCh38.p7	9:122893012	ACTTAACTTAATTGA[C/G]TGATGATCTGGTACC	54542
rs760361781	in-del	-/AA			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905867	ACTCTGTTTCTAGAC[-/AA]AGAGTCCAAAGTGGG	54542
rs760372073	snp	C/G	1.65715e-05	0.00287845	missense	RC3H2	GRCh38.p7	9:122892917	AACTTACCTTTACCT[C/G]CACTTAGTGGTTTTA	54542
rs760387954	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122889201	ATTTTTTTGTGATGT[A/G]AATTAAACACAAAAT	54542
rs760431612	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122903863	AAGGCATGTGAAGCT[A/T]CAACAGTGGTATAGC	54542
rs760440994	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895132	ATACCTGTTGACCTA[C/T]AGCAGATGCTAAATA	54542
rs760445027	snp	A/T	1.67075e-05	0.00289023	missense	RC3H2	GRCh38.p7	9:122854244	TTCTATGACCAGATA[A/T]ATCAGTAACAATGAA	54542
rs760469267	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122882592	ATCATAAAAACACTT[C/T]AAGGATTCAGCTTGC	54542
rs760527330	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122856472	ATTGCCTAGGCTGGT[A/G]TCAAACTCCTGGGCT	54542
rs760550647	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122871094	AATAATTTATCTTTC[C/T]GCTACCAATTCCAGT	54542
rs760639839	snp	C/T	1.65792e-05	0.00287912	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880157	AGAATGCTTTTTACT[C/T]TGGTTCTTATGACAC	54542
rs760677036	snp	C/G	3.31208e-05	0.00406931	missense	RC3H2	GRCh38.p7	9:122859951	GACTTCAAAGGGTAT[C/G]TGAGTCCTTGGATCT	54542
rs760677810	snp	C/T	1.65669e-05	0.00287805	synonymous-codon	RC3H2	GRCh38.p7	9:122851341	AATTGGTTCACTTTG[C/T]CCATCAGGTTCATCA	54542
rs760700639	snp	G/T	1.69268e-05	0.00290914	intron-variant	RC3H2	GRCh38.p7	9:122883390	CATAGCTAAAAATAT[G/T]AAAGGAACATGAGTT	54542
rs760730860	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881677	TTGCAGGGGTGGGGA[C/T]GGAGAGGACAGGGTC	54542
rs760752197	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122870719	CCATGCGTAACTCTC[C/T]CTATTCTTTTTAAAT	54542
rs760776273	snp	C/T	3.3129e-05	0.00406982	synonymous-codon	RC3H2	GRCh38.p7	9:122851221	ACCAAGCTGTATGTC[C/T]AAGATCTCCTAAGAA	54542
rs760789800	snp	A/G	1.67677e-05	0.00289544	synonymous-codon	RC3H2	GRCh38.p7	9:122855861	TTCAAATTTTGTACC[A/G]CTCACACTCTCTGAG	54542
rs760831259	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884530	ATCTGAAGTTAATCA[C/T]TGGAGAACATCAGAC	54542
rs760893003	in-del	-/TTT			intron-variant	RC3H2	GRCh38.p7	9:122860407	CCATTTACCCATTCT[-/TTT]TTTTTTTTTTTTTTT	54542
rs760935624	snp	A/G	1.66183e-05	0.00288251	intron-variant	RC3H2	GRCh38.p7	9:122877454	AACCCATATGAAACA[A/G]AATTCTCAACACTTA	54542
rs761018096	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122851470	TTGCTCTCCCTCTCC[C/T]TCTCCCTCTCCCCAT	54542
rs761050420	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876082	CTTGGATCACAAGGA[C/T]GGAAAGAAGAATAAA	54542
rs761060823	snp	C/T	8.27972e-05	0.00643364	missense	RC3H2	GRCh38.p7	9:122858856	GGTGGGCGCCAGATG[C/T]GCCTGCTGTCGTACA	54542
rs761076257	in-del	-/TCCCTCTCCCCA			intron-variant	RC3H2	GRCh38.p7	9:122851472	CTCTCCCTCTCCCTC[-/TCCCTCTCCCCA]TCCCTCTCCCCATGG	54542
rs761085969	snp	G/T	1.65765e-05	0.00287888	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897537	ATGCTCGGGTTAGCA[G/T]TCTAGCAGATCATTA	54542
rs761102363	snp	G/T	4.0085e-05	0.0044767	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880318	AGACACTTAGAAAAC[G/T]TATAAGCTGTATTAA	54542
rs761151292	snp	A/T	1.69677e-05	0.00291266	intron-variant	RC3H2	GRCh38.p7	9:122854665	AGTGAAAAATCAGTG[A/T]ACTGAGGTGAATGTA	54542
rs761199022	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122898106	ATCTCTGACAAGACT[C/T]GGCTAGGAAGCAAAA	54542
rs761204366	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122890722	TATAGTAATAAGAAG[A/C]CTAATTTTTAGCTAC	54542
rs761231075	snp	G/T	0.000217088	0.0104162	synonymous-codon	RC3H2	GRCh38.p7	9:122849774	AATAGACACTGGGAG[G/T]GGCTGGCTAAAGCAA	54542
rs761241636	in-del	-/AA			intron-variant, downstream-variant-500B	RC3H2	GRCh38.p7	9:122853378	CCAAGAATGATCAAT[-/AA]AAAAAAAAAAAAAAA	54542
rs761262631	snp	A/G	1.71905e-05	0.00293172	intron-variant	RC3H2	GRCh38.p7	9:122893039	TACCTTAAAAAAAAA[A/G]AAAAAGGAATATTGC	54542
rs761309135	in-del	-/GAG	0.000314697	0.0125399	cds-indel	RC3H2	GRCh38.p7	9:122857949	AGTCTACACTGAACA[-/GAG]GAGAAGGTGGTGTTG	54542
rs761329627	snp	A/G	1.66062e-05	0.00288146	missense	RC3H2	GRCh38.p7	9:122849695	CTTCAGACATAACAT[A/G]AGTTTTCAGAATGAG	54542
rs761362500	snp	A/G	1.65825e-05	0.00287941	missense	RC3H2	GRCh38.p7	9:122858713	CACTTGGTGGCTGAC[A/G]AGCCACCGAATAATA	54542
rs761381015	snp	A/G			utr-variant-5-prime	RC3H2	GRCh38.p7	9:122905159	TCCCGGGAGCCCCGC[A/G]ACGGCGCGGCTTGGC	54542
rs761392164	snp	C/T	3.35171e-05	0.00409358	synonymous-codon	RC3H2	GRCh38.p7	9:122854266	AACAATGAATCTGTC[C/T]CTTTAAAGAGAAATA	54542
rs761419253	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122870508	AAAAAAGAGTCAGGA[G/T]AAATAAAATCTTAAC	54542
rs761429326	snp	C/T	1.67837e-05	0.00289682	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880207	CAATTTATCAACATA[C/T]TTAATACGTTTTCAA	54542
rs761473992	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122877372	TGCCCAGCCCTTAAC[A/T]TGCATTTTTGAAAGT	54542
rs761475926	snp	C/T	1.65611e-05	0.00287755	missense	RC3H2	GRCh38.p7	9:122860054	GGCACAGAATTCAGC[C/T]CTGTTCCAACATTAG	54542
rs761482698	snp	A/T	1.66355e-05	0.002884	missense	RC3H2	GRCh38.p7	9:122849675	TTTTAAAAAGTCGTT[A/T]TTATCTTCAGACATA	54542
rs761484359	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122898908	TGAACAAGAAATCTA[C/G]GTATTTAGGGCAATC	54542
rs761490458	in-del	-/CAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870405	AAACAAACAAACAAA[-/CAAAC]AAACAAAAAAAAAAC	54542
rs761494379	snp	A/C	1.65847e-05	0.0028796	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880042	ATGAGGCCTCAGTCT[A/C]TTTAAGTTAGCTGGG	54542
rs761639775	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122865922	TTTTCCCCTCATGCC[A/C]CTTTGTCCAAGAATG	54542
rs761662113	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865880	TACATGTAATTAATA[C/T]AGCAAGCCGAGTTTA	54542
rs761684558	snp	A/G	3.33378e-05	0.00408262	intron-variant	RC3H2	GRCh38.p7	9:122860163	ACAAAGGGCAAAGGA[A/G]AAATCACTGTCTATG	54542
rs761714068	snp	A/G	1.87535e-05	0.00306209	intron-variant	RC3H2	GRCh38.p7	9:122855886	TCTGAGAACTGGTTA[A/G]AAAAAAATAAATAAA	54542
rs761731051	in-del	-/A	1.92445e-05	0.00310191	intron-variant	RC3H2	GRCh38.p7	9:122890595	TTTTCAATAAAAAAT[-/A]AAAGTCAATTTTCAT	54542
rs761744054	in-del	-/AACAAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870399	ACAAACAAACAAACA[-/AACAAACAAACAAAC]AAAAAAAAAACAACA	54542
rs761756560	snp	A/G	1.65619e-05	0.00287762	synonymous-codon	RC3H2	GRCh38.p7	9:122890427	TCTTTCTCCAAGGGA[A/G]CGAGCTGCTCGCATG	54542
rs761814731	snp	A/C	1.65633e-05	0.00287774	missense	RC3H2	GRCh38.p7	9:122877498	TCCTGAGAATGGGCA[A/C]ATGTACAATTTGTTC	54542
rs761823229	snp	A/T	6.24707e-05	0.00558851	intron-variant	RC3H2	GRCh38.p7	9:122890250	GATTCACCGAGCTCC[A/T]GAAATTGGCATCCTC	54542
rs761854048	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122864519	TAGTTTTATGAAGGA[A/G]TAAACTAAGGTAGAC	54542
rs761885993	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122879626	AACTGGGTTCCTCCC[-/A]AAAGAATAGAGATGA	54542
rs761912402	snp	A/G	3.31428e-05	0.00407066	synonymous-codon	RC3H2	GRCh38.p7	9:122851383	TGAAAGCTCTAACTC[A/G]ATATCCCTATCAGGT	54542
rs761932015	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122854905	GGCCAGGAGTTCCAG[A/C]CCAGCCTGGCCAACA	54542
rs761961584	snp	C/T	7.53494e-05	0.00613751	intron-variant	RC3H2	GRCh38.p7	9:122851477	CCCTCTCCCTCTCCC[C/T]CTCCCCATGGTCTCC	54542
rs762010954	snp	C/T	1.656e-05	0.00287745	missense	RC3H2	GRCh38.p7	9:122858878	TGTCGTACACAGGAG[C/T]ATACATTCCAGAAGG	54542
rs762015176	in-del	-/G			intron-variant	RC3H2	GRCh38.p7	9:122854325	GAAGCAACAAAAGCA[-/G]TAATAACCATATGTT	54542
rs762033387	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906690	TTTTAACAAAATATA[C/T]AGTTATTACCTATTA	54542
rs762064203	snp	C/T	4.9717e-05	0.00498558	missense	RC3H2	GRCh38.p7	9:122858977	GAGGGGAAAATGTAC[C/T]GTAATGATCGGCATA	54542
rs762089426	snp	A/G	1.65784e-05	0.00287905	synonymous-codon	RC3H2	GRCh38.p7	9:122855251	AGGATCTGTGGTATG[A/G]TAACCTGTACGGGAA	54542
rs762117719	snp	C/G	1.80562e-05	0.00300463	missense	RC3H2	GRCh38.p7	9:122859076	GAGCCACACCAGCTG[C/G]TACCGTTGGAGGTGG	54542
rs762135683	snp	A/G			intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853799	ATTTAAGAAATCTGG[A/G]ATTACAATTTTATTT	54542
rs762169630	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122872655	TTGGAGTGCAGTGGT[A/G]CTCACTGCAACCTCT	54542
rs762190559	snp	C/T	4.28495e-05	0.00462849	intron-variant	RC3H2	GRCh38.p7	9:122855139	AAAAAAAAAAAGGCA[C/T]AGTGCTTAGAACATA	54542
rs762205033	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122898308	AACTACATTATTTAG[C/T]GATTGATATATATAA	54542
rs762247821	snp	A/G	1.72018e-05	0.00293268	missense	RC3H2	GRCh38.p7	9:122849805	GAAGTTACCGGCAGA[A/G]TTGTTTTTTGCTCCT	54542
rs762275673	snp	C/T	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122865503	CATTTGAAATTCCGT[C/T]TGTACTTGGAACAAT	54542
rs762341640	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122886324	TGGACATTCGGATTG[C/T]TTCCACCTTTTGACT	54542
rs762366461	in-del	-/TCTCCCTCTCCCTCTCCCCATGG			intron-variant	RC3H2	GRCh38.p7	9:122851465	TGATTTTGCTCTCCC[-/TCTCCCTCTCCCTCTCCCCATGG]TCTCCCTCTCCCCAT	54542
rs762380266	snp	A/G	1.65625e-05	0.00287766	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880650	CACCATACAAAAGAG[A/G]GGACCACTGTTCAGG	54542
rs762502967	snp	A/G	1.65715e-05	0.00287845	synonymous-codon	RC3H2	GRCh38.p7	9:122854563	TGATGATGTGGCCTC[A/G]TTGCCATATGAACTC	54542
rs762526194	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122858605	GCCAGGATATATACC[-/T]TGGGTGGTTTGACTC	54542
rs762527921	snp	A/G	1.66056e-05	0.00288141	synonymous-codon	RC3H2	GRCh38.p7	9:122849693	ATCTTCAGACATAAC[A/G]TGAGTTTTCAGAATG	54542
rs762567402	snp	A/G	5.4756e-05	0.00523211	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880300	CCTATGAAATTCATC[A/G]TTAGACACTTAGAAA	54542
rs762567954	snp	C/G	0.000118017	0.00768079	missense	RC3H2	GRCh38.p7	9:122849781	ACTGGGAGTGGCTGG[C/G]TAAAGCAAGAAGTTA	54542
rs762577884	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122893433	CGGGAGGCTGAGGTT[A/G]CAGTGAGCTGAGATC	54542
rs762584760	snp	A/C	1.65644e-05	0.00287783	missense	RC3H2	GRCh38.p7	9:122860079	CATTAGAGGGCCCAG[A/C]TGAGGTAGCTGCTAC	54542
rs762624097	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122899347	TGCCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT	54542
rs762706024	in-del	-/TACT	1.65669e-05	0.00287805	intron-variant	RC3H2	GRCh38.p7	9:122883190	ATGTCTTTACATAGA[-/TACT]TACTGCTTACCTTAA	54542
rs762766656	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122869395	TTTAGTCCTCTGGTA[A/T]CTATAAACAACTTCA	54542
rs762818566	snp	C/T	1.65627e-05	0.00287769	missense	RC3H2	GRCh38.p7	9:122858018	GAGGTGCTTTCTGAG[C/T]GTGGTACTGTGCCCA	54542
rs762920551	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122901928	TGAGATAACTACTTC[-/T]TTTTTTTTTTTTTTT	54542
rs762924723	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122870571	ATACACTGAATTCTT[A/C]GTATTGGGGCAGCTA	54542
rs762926607	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122850089	TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG	54542
rs762935607	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122876954	AGCAAATAAGACTGC[A/G]AGTATTTTCATTCTG	54542
rs762960276	snp	A/G	3.92989e-05	0.0044326	missense	RC3H2	GRCh38.p7	9:122859088	CTGGTACCGTTGGAG[A/G]TGGTGGATAGTATCC	54542
rs762991165	in-del	-/CAAACAA			intron-variant	RC3H2	GRCh38.p7	9:122870405	AAACAAACAAACAAA[-/CAAACAA]ACAAAAAAAAAACAA	54542
rs763012905	snp	C/G	1.65649e-05	0.00287788	missense	RC3H2	GRCh38.p7	9:122853962	TTTACCTCTCCATTT[C/G]TTAGTTCAATTTCCT	54542
rs763039993	snp	C/G	1.65987e-05	0.00288082	intron-variant	RC3H2	GRCh38.p7	9:122892868	AAGTAAATGTACTAC[C/G]AAGTCCTACTTATCA	54542
rs763044287	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905388	TCGCGAGAAGTTACT[C/T]CCCACTTAACGCGAG	54542
rs763092991	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122896656	ATACCTATTACTGAA[C/T]AAAGTTCAATAACTA	54542
rs763230704	snp	C/G	4.97022e-05	0.00498484	missense	RC3H2	GRCh38.p7	9:122855264	TGGTAACCTGTACGG[C/G]AAGATCTGGAAATCG	54542
rs763280153	snp	A/C	1.65622e-05	0.00287764	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880714	AACAATTTGGGCATC[A/C]TGTTCTCTGCGTAAT	54542
rs763283723	snp	C/T	0.000115995	0.00761472	intron-variant	RC3H2	GRCh38.p7	9:122851054	GTCCTATGCCCACTG[C/T]TTATGAATTTTCTGT	54542
rs763311501	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122856660	AAGGAGGCTCTGGAG[A/G]TAAAGGGGAAATGAA	54542
rs763395132	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122859140	ATTTAATGTAATCTT[A/T]GTACAATCCAACATT	54542
rs763463677	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122888309	TTTTAGCTTTATTTT[G/T]AGGTATTATTTTGAT	54542
rs763491893	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122872735	GATTACAGGCGTGCA[A/C]CACCATGCCCGGCTA	54542
rs763543043	snp	C/G	1.66316e-05	0.00288367	missense	RC3H2	GRCh38.p7	9:122865642	GGCATTGATCTTTTT[C/G]TTCCTTAATCGATAC	54542
rs763568821	in-del	-/A	1.69268e-05	0.00290914	intron-variant	RC3H2	GRCh38.p7	9:122883390	ATAGCTAAAAATATT[-/A]AAAGGAACATGAGTT	54542
rs763570507	snp	C/T	1.6571e-05	0.0028784	synonymous-codon	RC3H2	GRCh38.p7	9:122892925	TTTACCTCCACTTAG[C/T]GGTTTTAAGTAGAGT	54542
rs763587970	snp	A/G	6.64386e-05	0.00576323	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879893	AATAAGCCACCAAGG[A/G]CATGGGGGTTGGGGG	54542
rs763597772	snp	C/T	0.000117682	0.00766988	intron-variant	RC3H2	GRCh38.p7	9:122875186	CCTTAATCCTCTTCT[C/T]TAGGCACTTCAAGTG	54542
rs763600703	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122889210	TGATGTAAATTAAAC[A/G]CAAAATTATATAGTC	54542
rs763625425	in-del	-/AGAAGGTGGTGTTGGTGACTGTGTTGC	1.66532e-05	0.00288554	intron-variant	RC3H2	GRCh38.p7	9:122860155	AAATTTAACAAAGGG[-/AGAAGGTGGTGTTGGTGACTGTGTTGC]CAAAGGAGAAATCAC	54542
rs763667857	in-del	-/GGCAATG			intron-variant	RC3H2	GRCh38.p7	9:122865721	CTCAAGACAAAAAAT[-/GGCAATG]GGCAATGGGAATAGA	54542
rs763676573	snp	C/T			missense	RC3H2	GRCh38.p7	9:122865590	TGACAGTGTTGTTTA[C/T]ACCAACTTTATTTAG	54542
rs763713828	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122868900	GTGTGTATGTGTTTT[-/T]TTTTTTTTTTTTTGT	54542
rs763737456	snp	A/C	1.66488e-05	0.00288515	missense	RC3H2	GRCh38.p7	9:122893015	TAACTTAATTGACTG[A/C]TGATCTGGTACCTTA	54542
rs763768661	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122874595	TAATCTCAGTTCACG[A/G]CAGACCTGACCTCCC	54542
rs763851703	snp	A/G	5.30096e-05	0.00514801	intron-variant	RC3H2	GRCh38.p7	9:122859141	TTTAATGTAATCTTA[A/G]TACAATCCAACATTT	54542
rs763866314	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122896365	AGTAACAACAACAAC[-/A]AAAAAACCTGTTTCT	54542
rs763915944	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895284	CCCATCTCACCATCT[C/T]AGCCTCCCAAGTAGG	54542
rs763962510	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122901258	ATGTGAGGAATATAA[C/G]CTACTGAAATGGACT	54542
rs763966518	snp	C/G	1.65633e-05	0.00287774	missense	RC3H2	GRCh38.p7	9:122851201	TGATCATTTTGAGAA[C/G]TGATACCAAGCTGTA	54542
rs764047022	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122864288	AAACAACTTTTCAGA[A/T]AATCTGAAAATTTAA	54542
rs764054435	in-del	-/TC			intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853814	GATTACAATTTTATT[-/TC]TGTTATAAGTTTTAA	54542
rs764098998	snp	C/T	1.65836e-05	0.0028795	missense	RC3H2	GRCh38.p7	9:122855740	ATCATACCATTAACA[C/T]AGCATTTGAATTAGC	54542
rs764138997	snp	A/C	8.47968e-05	0.00651085	intron-variant	RC3H2	GRCh38.p7	9:122883393	AGCTAAAAATATTAA[A/C]GGAACATGAGTTCAT	54542
rs764160029	snp	G/T	1.78717e-05	0.00298923	intron-variant	RC3H2	GRCh38.p7	9:122855883	CTCTCTGAGAACTGG[G/T]TAAAAAAAAATAAAT	54542
rs764196585	snp	C/T	0.000111938	0.00748041	intron-variant	RC3H2	GRCh38.p7	9:122875262	CACACACACTTATCT[C/T]CTCTCTATCACAATG	54542
rs764225196	snp	C/T	0.000154273	0.00878139	intron-variant	RC3H2	GRCh38.p7	9:122890242	AGTCTCAGGATTCAC[C/T]GAGCTCCAGAAATTG	54542
rs764251464	snp	G/T	1.65866e-05	0.00287976	intron-variant	RC3H2	GRCh38.p7	9:122877468	AGAATTCTCAACACT[G/T]ACTTTTCAAGCTCTT	54542
rs764254793	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122869229	ATTTTTAAAGCGGTG[-/A]AAAATTAAGTTCACG	54542
rs764256031	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122886275	TAGCCTATTTATGGA[A/T]ACATTACATTTTGTT	54542
rs764272888	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122876981	TCTGCACAGGTGCTC[A/G]GTATAAATATGGATT	54542
rs764306822	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122850427	TACTATATTATATGC[C/T]ATCTATCTATAGATA	54542
rs764328223	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122858751	AATGAGTTATATCTT[C/T]CCCGCAAAGATGTCT	54542
rs764335454	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903543	AAGGACGTAAGTCTT[C/T]TTACATGTCAGGTTA	54542
rs764381597	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122871079	ATGAAAGCAGAGGAG[A/C]ATAATTTATCTTTCC	54542
rs764420991	snp	A/C	1.65688e-05	0.00287821	missense	RC3H2	GRCh38.p7	9:122854580	TGCCATATGAACTCC[A/C]CCTTGAATCAACAGC	54542
rs764426949	snp	A/G	0.000102449	0.00715638	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880240	GTCTTCAGATTCCAC[A/G]GTAGGAGTATCAGTG	54542
rs764492836	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122876366	GGTGTGGTGGCTCAC[A/G]TCTGTAATCCCAGTA	54542
rs764493043	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857309	CTCCAAATATAACAG[C/T]ACTGAAAACACCAGA	54542
rs764525874	snp	A/G	1.66377e-05	0.00288419	synonymous-codon	RC3H2	GRCh38.p7	9:122897426	ACAACCTAAACTGAT[A/G]GGTTTGTGCACATTC	54542
rs764537539	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886318	ACTTGATGGACATTC[A/G]GATTGTTTCCACCTT	54542
rs764596456	snp	A/G	1.67798e-05	0.00289648	intron-variant	RC3H2	GRCh38.p7	9:122854271	TGAATCTGTCCCTTT[A/G]AAGAGAAATATGTTT	54542
rs764598082	snp	C/T	0.000161668	0.00898933	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880319	GACACTTAGAAAACT[C/T]ATAAGCTGTATTAAC	54542
rs764615819	snp	A/T	1.65877e-05	0.00287986	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897540	CTCGGGTTAGCAGTC[A/T]AGCAGATCATTATTT	54542
rs764633026	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122855134	AAAAAAAAAAAAAAA[A/G]GGCATAGTGCTTAGA	54542
rs764635629	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892347	CAAACTCCTGGGCTC[A/G]AGAAATCTACCCACC	54542
rs764661006	snp	C/T	3.32066e-05	0.00407458	missense	RC3H2	GRCh38.p7	9:122849700	GACATAACATGAGTT[C/T]TCAGAATGAGGTTGC	54542
rs764672649	snp	C/T	0.000165653	0.00909941	missense	RC3H2	GRCh38.p7	9:122865376	GAATCTGCAGAGGGC[C/T]CAGCAGCATTCTGAC	54542
rs764704735	snp	A/G	1.74759e-05	0.00295595	intron-variant	RC3H2	GRCh38.p7	9:122893048	AAAAAAAAAAAAGGA[A/G]TATTGCAGAAATACA	54542
rs764724224	snp	C/G	3.41082e-05	0.00412952	missense	RC3H2	GRCh38.p7	9:122849799	AAGCAAGAAGTTACC[C/G]GCAGAATTGTTTTTT	54542
rs764732757	in-del	-/AGA	1.65615e-05	0.00287758	cds-indel	RC3H2	GRCh38.p7	9:122858942	AGGAGGCTGGTAAGG[-/AGA]AGAATTCATTCGATC	54542
rs764749498	snp	A/G	3.31203e-05	0.00406928	missense	RC3H2	GRCh38.p7	9:122859974	TTGGATCTTGAAAAT[A/G]CTGAATGTTTTCAGA	54542
rs764792589	in-del	-/A	1.6585e-05	0.00287962	intron-variant	RC3H2	GRCh38.p7	9:122854101	CCTATATGAGGAGGG[-/A]AAAAAAGAAAAGTTA	54542
rs764793276	snp	A/G	1.65864e-05	0.00287974	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880048	CCTCAGTCTATTTAA[A/G]TTAGCTGGGTCACCT	54542
rs764793507	snp	C/G	1.66156e-05	0.00288228	synonymous-codon	RC3H2	GRCh38.p7	9:122897297	GGCTCCAACTAACTG[C/G]AGAAGTGCGAAGTTG	54542
rs764815727	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122859710	AACCCCTAAAGTTCA[C/T]TCCTGACCCTATTAT	54542
rs764817843	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122893448	GCAGTGAGCTGAGAT[A/C]GCACCAGTGCACTCC	54542
rs764933345	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122864752	CAGCCTCCTGAGTAG[C/T]TGGGACTACATATGC	54542
rs764950140	snp	A/G	1.65614e-05	0.00287757	missense	RC3H2	GRCh38.p7	9:122860070	CTGTTCCAACATTAG[A/G]GGGCCCAGCTGAGGT	54542
rs765057565	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122902898	TTATTTTTAGTAATA[C/T]ATTTTATTTATCCCA	54542
rs765058516	snp	A/G	1.65787e-05	0.00287907	missense	RC3H2	GRCh38.p7	9:122857931	TTCTTACATCCGCAC[A/G]AAAGTCTACACTGAA	54542
rs765070255	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122882667	TACATTTTAAAATAT[C/T]TTGGGGTTCTTCTCT	54542
rs765082700	in-del	-/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881281	ACTTGAAGTCAGGAG[-/T]TTTGAGACCAGCCTG	54542
rs765101312	snp	A/G	1.65625e-05	0.00287766	synonymous-codon	RC3H2	GRCh38.p7	9:122877506	ATGGGCAAATGTACA[A/G]TTTGTTCCTCGTGGA	54542
rs765138819	snp	G/T	6.81861e-05	0.00583853	intron-variant	RC3H2	GRCh38.p7	9:122883400	AATATTAAAGGAACA[G/T]GAGTTCATGACAAAT	54542
rs765141020	snp	A/T	9.50146e-05	0.0068919	intron-variant	RC3H2	GRCh38.p7	9:122855894	CTGGTTAAAAAAAAA[A/T]AAATAAAGCCAATTA	54542
rs765155896	in-del	-/GAG			intron-variant	RC3H2	GRCh38.p7	9:122867101	CCAGCCGCCCCGTCT[-/GAG]AAGGGAGGAGACCCT	54542
rs765177702	snp	A/G	1.69559e-05	0.00291164	synonymous-codon	RC3H2	GRCh38.p7	9:122849792	CTGGCTAAAGCAAGA[A/G]GTTACCGGCAGAATT	54542
rs765237126	snp	C/T	3.31444e-05	0.00407076	missense	RC3H2	GRCh38.p7	9:122851388	GCTCTAACTCGATAT[C/T]CCTATCAGGTTTAGT	54542
rs765275242	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122871654	AAGAGTCTTTCCTAC[A/C]CTATTCTATCTAAGA	54542
rs765284341	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122904183	GGGGGAGAGTAGAAA[G/T]GAAAAAAAGGAAGGC	54542
rs765290342	snp	C/T	3.93468e-05	0.0044353	intron-variant	RC3H2	GRCh38.p7	9:122851485	CTCTCCCTCTCCCCA[C/T]GGTCTCCCTCTCCCC	54542
rs765352603	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122900235	ATACCTTTAAGATAT[A/G]AAGGTAAAACACTGC	54542
rs765370546	snp	A/G	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858888	AGGAGCATACATTCC[A/G]GAAGGTACTGGAGGA	54542
rs765396428	snp	A/G	0.00019915	0.00997675	intron-variant	RC3H2	GRCh38.p7	9:122877630	CAAGGTGAAGATTCC[A/G]TTTGTTATTCACTCT	54542
rs765407197	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122872687	CCTCCCAGGTTCACG[C/T]GATTCTCGTGCCTCA	54542
rs765426110	snp	A/T	1.6588e-05	0.00287988	missense	RC3H2	GRCh38.p7	9:122854603	TCAACAGCATTGACA[A/T]AAGGGACATAATCTA	54542
rs765465780	snp	A/C/T	5.19668e-05	0.00509717	missense	RC3H2	GRCh38.p7	9:122849809	TTACCGGCAGAATTG[A/C/T]TTTTTGCTCCTCCCT	54542
rs765466485	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122893977	TATAAAAGTTCAATA[C/T]AGGCCAGGTGCGGTG	54542
rs765475418	snp	C/T	3.72252e-05	0.00431407	intron-variant	RC3H2	GRCh38.p7	9:122855146	AAAAGGCATAGTGCT[C/T]AGAACATATCAGGCT	54542
rs765517797	snp	C/T	3.46963e-05	0.00416497	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897558	CAGATCATTATTTTG[C/T]TGTGTAGTGTTTTGT	54542
rs765586981	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122898309	ACTACATTATTTAGC[A/G]ATTGATATATATAAC	54542
rs765726062	snp	A/T	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122865506	TTGAAATTCCGTTTG[A/T]ACTTGGAACAATTTT	54542
rs765763965	snp	A/G	1.65614e-05	0.00287757	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880688	CGGAGTCCTGCTTCC[A/G]TGGCAATATGAACAA	54542
rs765770728	snp	C/T	1.65798e-05	0.00287917	intron-variant	RC3H2	GRCh38.p7	9:122851042	TCTCTTTATTATGTC[C/T]TATGCCCACTGTTTA	54542
rs765864935	in-del	-/AAGA			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881020	ATTTCAGCCACTAGT[-/AAGA]AAGAGAAACTTGTAA	54542
rs765874070	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886347	TTTTGACTATTGTGA[A/G]TAACGCTGCAATAAA	54542
rs765880120	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880968	CTGGAACAAAACAGA[A/G]CTTACATAACTAAAT	54542
rs765928195	snp	G/T	1.66021e-05	0.0028811	intron-variant	RC3H2	GRCh38.p7	9:122855920	AATTAGTAAGAAGCT[G/T]AAATTTACAAGCTTG	54542
rs765944070	snp	A/G	1.85517e-05	0.00304557	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880303	ATGAAATTCATCATT[A/G]GACACTTAGAAAACT	54542
rs765944081	snp	A/T	1.65644e-05	0.00287783	synonymous-codon	RC3H2	GRCh38.p7	9:122860080	ATTAGAGGGCCCAGC[A/T]GAGGTAGCTGCTACA	54542
rs765964367	snp	A/C	1.70845e-05	0.00292267	intron-variant	RC3H2	GRCh38.p7	9:122865336	CCAGTAATCATTTTT[A/C]CCTAATACCTACTTT	54542
rs765980469	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122879664	TTATGAGTCACATAC[A/G]GAGTCCAATTAACAA	54542
rs766033195	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905416	GAGATTACGCAAGCC[C/T]GGGAGTCGGGAGTTG	54542
rs766057890	snp	C/G	1.6566e-05	0.00287797	synonymous-codon	RC3H2	GRCh38.p7	9:122857947	AAAGTCTACACTGAA[C/G]AGAGGAGAAGGTGGT	54542
rs766130123	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122850101	CCTGCCTCAGCCTCC[A/C]AAGTAGCTGGGATTA	54542
rs766167479	snp	A/G	1.75505e-05	0.00296225	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879726	GAGTTAGAGACAACA[A/G]CAGTCAGAAATGTAA	54542
rs766194577	snp	C/T	1.65644e-05	0.00287783	missense	RC3H2	GRCh38.p7	9:122853969	CTCCATTTCTTAGTT[C/T]AATTTCCTTGCTTAA	54542
rs766214532	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122878924	TGGCTCATTTTTGTA[-/T]TTTTTTTTTTTTAGT	54542
rs766252061	snp	C/T	7.51343e-05	0.00612874	intron-variant	RC3H2	GRCh38.p7	9:122890275	ATCCTCAAGCCCCAA[C/T]AGCTAATAAAAAAGG	54542
rs766252718	snp	C/T	1.85879e-05	0.00304854	intron-variant, utr-variant-3-prime	RC3H2	GRCh38.p7	9:122853855	ATCATCCATCAGAGA[C/T]AGGCACACCAAAATG	54542
rs766339939	snp	C/T	1.65633e-05	0.00287774	synonymous-codon	RC3H2	GRCh38.p7	9:122890463	TACACGACCTTCTTC[C/T]TCCACCAGTTGACAG	54542
rs766346088	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122873800	GTTTTATAACTATAC[C/T]ATAATTTTTATTTAT	54542
rs766367049	snp	A/G	1.65993e-05	0.00288086	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879858	TCCAGCTGCTCCCAA[A/G]TTGGTGAAACAGCGT	54542
rs766448063	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122851313	TCAATTATCTAATTG[C/T]GGCACTTACTTCAAT	54542
rs766507132	snp	C/T	0.000123385	0.00785349	intron-variant	RC3H2	GRCh38.p7	9:122855161	TAGAACATATCAGGC[C/T]AGGTATTATCTAAAT	54542
rs766562631	snp	C/T	3.31301e-05	0.00406989	synonymous-codon	RC3H2	GRCh38.p7	9:122855278	GGAAGATCTGGAAAT[C/T]GCACCCCATTTTGAG	54542
rs766615579	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881760	GACTTTCTGGGCTCA[A/G]GCAATCCTCTCGCTT	54542
rs766617717	snp	C/G/T	6.62837e-05	0.00575657	intron-variant	RC3H2	GRCh38.p7	9:122851056	CCTATGCCCACTGTT[C/G/T]ATGAATTTTCTGTCT	54542
rs766630552	in-del	-/AT			intron-variant	RC3H2	GRCh38.p7	9:122862213	TTATAGAAAAAGCTA[-/AT]CTTCAAGGCAACAAG	54542
rs766670648	snp	C/T	1.65627e-05	0.00287769	missense	RC3H2	GRCh38.p7	9:122851159	TGTACTGGATGCCCA[C/T]TTTCCACTGCCATTC	54542
rs766689712	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122886420	TTTTGGGTATATACC[G/T]AGGAATAAAACTGCT	54542
rs766723375	snp	C/T	6.6246e-05	0.00575488	synonymous-codon	RC3H2	GRCh38.p7	9:122865540	TGTTGTTTCAGTACT[C/T]CCTATGACAGAAATG	54542
rs766744622	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122874287	AGGATGAGATTCTGT[C/G]ATGTACTGAGGAACT	54542
rs766773027	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122900906	TTAAAGGTGGGACCA[C/T]AAACAATTTTTCGCT	54542
rs766828607	in-del	-/AATCTT	1.67497e-05	0.00289389	intron-variant	RC3H2	GRCh38.p7	9:122858115	GGGGATAAAAGAAAC[-/AATCTT]AATCATCTAGGGAGT	54542
rs766885822	in-del	-/TCTCCC	4.02459e-05	0.00448568	intron-variant	RC3H2	GRCh38.p7	9:122851487	TCCCTCTCCCCATGG[-/TCTCCC]TCTCCCTCTCCCCAT	54542
rs766886518	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906987	ATATACATACATATA[A/G]ATATATATACACATA	54542
rs766910765	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122873027	TATTTATTTTATGTT[A/T]ACATATAATAAATAT	54542
rs766941524	snp	A/G	1.65836e-05	0.0028795	intron-variant	RC3H2	GRCh38.p7	9:122854130	TAGCTTCCAACTATA[A/G]CTTTCAACTGTCATT	54542
rs766956766	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122901072	TATTAGTCCACCATA[G/T]TATGCAGCCAGTTCA	54542
rs766975613	snp	G/T	1.78819e-05	0.00299009	intron-variant	RC3H2	GRCh38.p7	9:122858631	GACTCCAGACACTGG[G/T]CTGTTAATGACTACA	54542
rs767001390	snp	C/T	3.31235e-05	0.00406948	missense	RC3H2	GRCh38.p7	9:122865500	CTGCATTTGAAATTC[C/T]GTTTGTACTTGGAAC	54542
rs767026948	snp	C/T	3.31521e-05	0.00407123	synonymous-codon	RC3H2	GRCh38.p7	9:122858717	TGGTGGCTGACAAGC[C/T]ACCGAATAATATCCA	54542
rs767040134	snp	C/G	1.65734e-05	0.00287862	missense	RC3H2	GRCh38.p7	9:122890495	TTACAAGTGTCACCA[C/G]TTTCCTTTGCATTGG	54542
rs767081327	snp	A/T	1.65649e-05	0.00287788	synonymous-codon	RC3H2	GRCh38.p7	9:122857956	ACTGAACAGAGGAGA[A/T]GGTGGTGTTGGTGAC	54542
rs767130694	snp	C/T	1.71308e-05	0.00292662	intron-variant, stop-lost	RC3H2	GRCh38.p7	9:122853874	CACACCAAAATGCAC[C/T]CAGTAATGGTATAAC	54542
rs767134573	snp	C/T	1.65679e-05	0.00287814	missense	RC3H2	GRCh38.p7	9:122858059	TTTCTTCTTATCTGC[C/T]CCTCGCAACTGGTCT	54542
rs767183931	snp	G/T	1.65647e-05	0.00287786	missense	RC3H2	GRCh38.p7	9:122853995	CTTAAAAGGTTTAAG[G/T]TAAGGTGACGGCCTT	54542
rs767206703	in-del	-/CTGC			intron-variant	RC3H2	GRCh38.p7	9:122871721	TGTTTTTTTTTCATA[-/CTGC]CTGTCATTACAAGAT	54542
rs767356938	snp	A/G	1.65627e-05	0.00287769	synonymous-codon	RC3H2	GRCh38.p7	9:122855311	GATGGGTCCATCACT[A/G]AAGGGAATTATTGGA	54542
rs767373724	in-del	-/TAC	1.65993e-05	0.00288086	intron-variant	RC3H2	GRCh38.p7	9:122892861	CATTCAAAGTAAATG[-/TAC]TACTACCAAGTCCTA	54542
rs767405200	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878163	CCTAGGATGAAAACA[C/T]TTGTTTTTAATATTT	54542
rs767483903	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122883023	CTCTTATTTTGCCAA[C/T]AGATAGTAATGGGTA	54542
rs767511174	snp	C/T	2.73774e-05	0.00369972	intron-variant	RC3H2	GRCh38.p7	9:122859112	AGTATCCTTGAAAAT[C/T]GGAAAGAGGAATATT	54542
rs767537117	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122896828	AGGAGCTCCAGACCA[C/G]CCTGGCCAACATAGT	54542
rs767541795	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122897719	TCTTTTTTAAAAAAC[C/G]TATTTGCTGAATTAA	54542
rs767564661	snp	A/G	1.65605e-05	0.0028775	synonymous-codon	RC3H2	GRCh38.p7	9:122859936	CTGTGGGTACTGTGG[A/G]ACTTCAAAGGGTATC	54542
rs767566476	snp	A/C/T	4.97781e-05	0.00498864	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879835	TTTTAACAGCTACCA[A/C/T]TGCATTTTCCAGCTG	54542
rs767622287	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122898054	TATTGTAGAGACTCA[A/G]GTGTGAAGAAAACAG	54542
rs767643203	snp	A/T	0.000109379	0.00739444	intron-variant	RC3H2	GRCh38.p7	9:122875210	TCAAGTGGGGAAAAA[A/T]ACTGAGAAGAGAAGC	54542
rs767664158	snp	C/T	1.66852e-05	0.0028883	missense	RC3H2	GRCh38.p7	9:122883371	GCTTCAAGGCCTCTT[C/T]TTGCATAGCTAAAAA	54542
rs767676395	in-del	-/AAGC			intron-variant	RC3H2	GRCh38.p7	9:122860513	TGACCTCCTGGGCTT[-/AAGC]AATCCTCCCACCTCA	54542
rs767693716	snp	A/C	1.66682e-05	0.00288684	intron-variant	RC3H2	GRCh38.p7	9:122855715	CTCCAACCCCTGCAA[A/C]CCCAGCAAAATCATA	54542
rs767697829	snp	C/G	1.65721e-05	0.0028785	intron-variant	RC3H2	GRCh38.p7	9:122883174	TGTCTCACAAACAGG[C/G]ATGTCTTTACATAGA	54542
rs767734712	snp	A/G	1.69602e-05	0.00291201	intron-variant	RC3H2	GRCh38.p7	9:122865675	GTTTCAAAAACAATC[A/G]ACAGATTGGTGAATA	54542
rs767744764	snp	C/T	3.31257e-05	0.00406962	synonymous-codon	RC3H2	GRCh38.p7	9:122851179	CACTGCCATTCCATT[C/T]AGCAACTGATCATTT	54542
rs767757937	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122877263	AGAGACGGGGGTCTC[C/T]TTATCTTGCCCAGGC	54542
rs767825201	snp	C/T	1.78892e-05	0.0029907	intron-variant	RC3H2	GRCh38.p7	9:122893070	AGAAATACATTCATC[C/T]AGCTCATGCAACTAT	54542
rs767833942	snp	A/G	9.94085e-05	0.00704942	synonymous-codon	RC3H2	GRCh38.p7	9:122858723	CTGACAAGCCACCGA[A/G]TAATATCCATCTAAT	54542
rs767848002	in-del	-/TCTCCCTCTCCCTCTCCCCATGGTCTCCCTCTCCCCATGG	1.8313e-05	0.00302592	intron-variant	RC3H2	GRCh38.p7	9:122851465	TGATTTTGCTCTCCC[lengthTooLong]TCTCCCTCTCCCTCT	54542
rs767863253	snp	A/G	1.78172e-05	0.00298468	intron-variant	RC3H2	GRCh38.p7	9:122858637	AGACACTGGGCTGTT[A/G]ATGACTACATTATAG	54542
rs767870927	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122854841	GGCACAGTGGCTCAC[-/A]ATATGTAATCCCAGC	54542
rs767920143	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889075	TGTTGGTCTTTTTCT[C/T]CTGAATTTTTAGACA	54542
rs767998842	snp	A/G	3.31813e-05	0.00407302	synonymous-codon	RC3H2	GRCh38.p7	9:122897402	GCAGGTCTTGCAAAC[A/G]GTGTGTGAACAACCT	54542
rs768041988	snp	G/T	3.31203e-05	0.00406928	missense	RC3H2	GRCh38.p7	9:122858841	TCTCGTTGGTACATA[G/T]GTGGGCGCCAGATGC	54542
rs768094682	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122895507	CTATGATATTTTATC[A/C]AATCTAAAATGTTGT	54542
rs768114790	snp	A/G	1.68055e-05	0.0028987	intron-variant	RC3H2	GRCh38.p7	9:122854278	GTCCCTTTAAAGAGA[A/G]ATATGTTTATTGTAA	54542
rs768144003	snp	C/T	1.65707e-05	0.00287838	intron-variant	RC3H2	GRCh38.p7	9:122851303	ACAAAGCCTCTCAAT[C/T]ATCTAATTGTGGCAC	54542
rs768169909	snp	A/G	3.31367e-05	0.00407029	synonymous-codon	RC3H2	GRCh38.p7	9:122854569	TGTGGCCTCGTTGCC[A/G]TATGAACTCCACCTT	54542
rs768214015	snp	A/G	3.37678e-05	0.00410886	intron-variant	RC3H2	GRCh38.p7	9:122897273	AGTAAAATCTTGAAT[A/G]CTTACCTGGGCTCCA	54542
rs768218745	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122870135	ATCCCAGCACCTTGG[C/G]AGGCTGAGGCGAGTG	54542
rs768220021	snp	A/G	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858810	TGGAGGTAAAGAATT[A/G]CTTCTAATAATGTCA	54542
rs768324007	snp	A/G	1.65858e-05	0.00287969	synonymous-codon	RC3H2	GRCh38.p7	9:122858711	CTCACTTGGTGGCTG[A/G]CAAGCCACCGAATAA	54542
rs768341711	snp	C/T	9.75753e-05	0.00698413	intron-variant	RC3H2	GRCh38.p7	9:122875183	ACTCCTTAATCCTCT[C/T]CTCTAGGCACTTCAA	54542
rs768354115	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122850758	AGAAAATCTTAACAT[G/T]ATTTTCAAAAAGAGA	54542
rs768375592	snp	A/T	1.65803e-05	0.00287922	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880162	GCTTTTTACTTTGGT[A/T]CTTATGACACATTTA	54542
rs768385342	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122904997	CCCAACCCTCGAGGC[A/G]CCAGGGGCGACAGCG	54542
rs768422967	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122896570	AAGAAAATCTTTCGC[A/G]GAATACAATCATGAA	54542
rs768426276	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122883783	GCCCAGGAGTTTGAG[A/G]CCAGTTTGGGTAATA	54542
rs768467264	in-del	-/TAACA			intron-variant	RC3H2	GRCh38.p7	9:122869440	TCTTCTCCTTCTCTT[-/TAACA]TGTACACATTGGCAG	54542
rs768480008	snp	A/G	0.000102757	0.00716714	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897511	GCCTGCACAGGCATT[A/G]TGGAAGCTGGATGCT	54542
rs768482951	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849359	CAAACTCATAAAAAG[A/C]TGCTTGAAGCTTAAG	54542
rs768570419	snp	C/T	8.32258e-05	0.00645027	missense	RC3H2	GRCh38.p7	9:122849671	CAGGTTTTAAAAAGT[C/T]GTTTTTATCTTCAGA	54542
rs768582960	snp	C/T	2.32886e-05	0.00341229	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897527	TGGAAGCTGGATGCT[C/T]GGGTTAGCAGTCTAG	54542
rs768624099	snp	C/T	1.74564e-05	0.0029543	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880273	GAATTAAATTTTCAC[C/T]TCAGAATCTGCCCTA	54542
rs768671508	snp	A/G	4.99917e-05	0.00499933	intron-variant	RC3H2	GRCh38.p7	9:122860161	TAACAAAGGGCAAAG[A/G]AGAAATCACTGTCTA	54542
rs768692756	snp	A/T	3.31208e-05	0.00406931	missense	RC3H2	GRCh38.p7	9:122860033	AGAAATGGGCTGGAT[A/T]TTTGAGGCACAGAAT	54542
rs768728830	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122868896	GTGTGTGTGTATGTG[-/TT]TTTTTTTTTTTTTTT	54542
rs768746715	in-del	-/CTCTCCCTCTCC	3.45802e-05	0.004158	intron-variant	RC3H2	GRCh38.p7	9:122851458	AAAATACTGATTTTG[-/CTCTCCCTCTCC]CTCTCCCTCTCCCCA	54542
rs768759914	snp	C/G	1.83694e-05	0.00303057	intron-variant	RC3H2	GRCh38.p7	9:122851472	GCTCTCCCTCTCCCT[C/G]TCCCTCTCCCCATGG	54542
rs768799183	snp	C/T	6.64066e-05	0.00576185	synonymous-codon	RC3H2	GRCh38.p7	9:122857926	AACCTTTCTTACATC[C/T]GCACGAAAGTCTACA	54542
rs768815099	in-del	-/AT	1.68869e-05	0.00290571	intron-variant	RC3H2	GRCh38.p7	9:122855683	ACAACATGAGTGAAC[-/AT]ATGCATCATCTCTCA	54542
rs768844978	in-del	-/TTTT			intron-variant	RC3H2	GRCh38.p7	9:122859253	GCTTTATACCCTGGC[-/TTTT]TTTTTTTTTTTTTTT	54542
rs768895683	snp	A/G	1.73664e-05	0.00294667	intron-variant	RC3H2	GRCh38.p7	9:122890567	GAAAAGGGAAACAAA[A/G]GGAGCTAAAGTTTTT	54542
rs768896451	snp	C/T	1.65762e-05	0.00287886	missense	RC3H2	GRCh38.p7	9:122892963	CCTCAACGCATTTCT[C/T]TGCAACCTCATAGTG	54542
rs768897664	snp	A/G	6.63295e-05	0.0057585	intron-variant	RC3H2	GRCh38.p7	9:122877611	GAACACATTCAATGA[A/G]TGGCAAGGTGAAGAT	54542
rs768941855	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892353	CCTGGGCTCAAGAAA[C/T]CTACCCACCTTAGCC	54542
rs769001622	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122887104	TCCCCAGTAACCTCT[C/T]GTCTAATGGGTTTAA	54542
rs769006184	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122877324	TCCTGCCTCAGCCCC[A/G]CAAACTGCTGGGACT	54542
rs769013134	snp	C/G	1.74845e-05	0.00295668	missense	RC3H2	GRCh38.p7	9:122859064	GAGGAACACAGGGAG[C/G]CACACCAGCTGGTAC	54542
rs769048602	snp	C/T	3.31362e-05	0.00407026	intron-variant, missense	RC3H2	GRCh38.p7	9:122853930	ACATTAAGCATGAAG[C/T]CGAAAGGTTCAGTTT	54542
rs769057079	snp	A/T	1.65946e-05	0.00288046	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879816	ACAAGGCCATGAACT[A/T]CTGTTTTAACAGCTA	54542
rs769066511	snp	G/T	1.66879e-05	0.00288855	missense	RC3H2	GRCh38.p7	9:122855215	CTTAGTCGCACTTCC[G/T]TGGGAAGCAGTGGCC	54542
rs769103595	in-del	-/A			intron-variant	RC3H2	GRCh38.p7	9:122885423	AGAGCTTAAGAGCTG[-/A]AAGATTATCTAGATT	54542
rs769110706	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122891839	TATACCTATGATGTG[C/T]TAAGTATGCAGTGAT	54542
rs769116312	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122860895	GATTAGCTGAAATAT[A/G]AACTCCTTGAGGAAA	54542
rs769119757	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861197	TTAACTCCTTTTAAG[A/G]AGTCAAATTTCGGCC	54542
rs769160437	snp	C/T	1.65636e-05	0.00287776	missense	RC3H2	GRCh38.p7	9:122851090	ACTCACAGAATCACA[C/T]GGTCTTCACCTAAAC	54542
rs769167647	snp	A/C/T	1.83741e-05	0.00303096	synonymous-codon	RC3H2	GRCh38.p7	9:122859080	CACACCAGCTGGTAC[A/C/T]GTTGGAGGTGGTGGA	54542
rs769418235	snp	A/C			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906366	TGAAACCCTGGCTCT[A/C]CTAAAAATACAAAAA	54542
rs769454372	snp	C/T	1.65864e-05	0.00287974	missense	RC3H2	GRCh38.p7	9:122854543	TACCTTTCAACATAG[C/T]GTGCTGATGATGTGG	54542
rs769465642	snp	A/T	1.77187e-05	0.00297641	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880289	TCAGAATCTGCCCTA[A/T]GAAATTCATCATTAG	54542
rs769483721	snp	C/T	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858831	AATAATGTCATCTCG[C/T]TGGTACATAGGTGGG	54542
rs769507491	snp	C/T	3.32618e-05	0.00407797	missense	RC3H2	GRCh38.p7	9:122849677	TTAAAAAGTCGTTTT[C/T]ATCTTCAGACATAAC	54542
rs769528407	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122897867	CGACCACATCAAACA[A/G]GCAAATTAACTTTCC	54542
rs769557163	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876606	GCACTCCACCCTGGG[C/T]GACAGAGCAAGACTC	54542
rs769578376	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122893282	CAGATTAACTTAAGT[G/T]AGGAGTTTGAGACCA	54542
rs769622350	snp	A/T	1.67357e-05	0.00289268	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880567	TAACAGCAATGATAG[A/T]ACATCAGCATCTCTA	54542
rs769626905	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905676	AAAGCGTGGAATCCA[C/T]TGAGCAGAATCTGAT	54542
rs769693366	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122879123	AATTTCGGCCAGGCA[C/T]GATGGCTCACGCCTG	54542
rs769738398	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122886072	TTTTTCTATTTTCAG[A/T]AGAGACAGAGTTTTC	54542
rs769761691	in-del	-/CAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870401	AAACAAACAAACAAA[-/CAAACAAAC]AAACAAAAAAAAAAC	54542
rs769792422	snp	A/G	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122890440	GAACGAGCTGCTCGC[A/G]TGGCTCTTACACGAC	54542
rs769801182	snp	A/G	1.76443e-05	0.00297016	intron-variant	RC3H2	GRCh38.p7	9:122890574	GAAACAAAGGGAGCT[A/G]AAGTTTTTTCAATAA	54542
rs769821496	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122860979	CCTGGAACAGAGTAG[A/G]CACTTGGTAAATATT	54542
rs770039210	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122887154	CTGAAGCCCATTAAT[A/T]CATTTGGGGATGTAA	54542
rs770056124	snp	C/T	1.65957e-05	0.00288055	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879948	TTGTGTTATTCACCT[C/T]AAAAGTAGAAAAAAA	54542
rs770089982	snp	C/T	4.97129e-05	0.00498538	synonymous-codon	RC3H2	GRCh38.p7	9:122855257	TGTGGTATGGTAACC[C/T]GTACGGGAAGATCTG	54542
rs770090070	snp	C/T	3.31406e-05	0.00407053	intron-variant	RC3H2	GRCh38.p7	9:122859903	TTTTCTTAGAATTGT[C/T]TAAAATTACTCACCT	54542
rs770134440	snp	C/T	1.65658e-05	0.00287795	synonymous-codon	RC3H2	GRCh38.p7	9:122854060	AGCATTGGCCTCTCT[C/T]TGAAGAAGTAATGAG	54542
rs770158581	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122874127	CAGATAAAGAGGAGA[C/G]AGAAAATAATACAAT	54542
rs770215461	in-del	-/TC	1.65622e-05	0.00287764	frameshift-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880717	ATTTGGGCATCATGT[-/TC]TCTCTGCGTAATGCT	54542
rs770254107	snp	A/G	1.65627e-05	0.00287769	missense	RC3H2	GRCh38.p7	9:122851150	TGGTGCTGCTGTACT[A/G]GATGCCCATTTTCCA	54542
rs770259911	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122862235	AGGCAACAAGATCCA[C/T]GATAAGGTCAACATT	54542
rs770337185	snp	C/T	1.66145e-05	0.00288218	missense	RC3H2	GRCh38.p7	9:122855808	CAGGAGCCTATGGTG[C/T]CACAAGACCAGGGAG	54542
rs770351883	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122885883	TTTTGTTTTGTTTTG[-/TT]TTGTTTGTTTTGTTT	54542
rs770367155	snp	G/T	1.81585e-05	0.00301313	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880826	AGAAAAATCAGAATT[G/T]GTCTGTGCTTTCTCC	54542
rs770453265	snp	C/T	1.65616e-05	0.00287759	synonymous-codon	RC3H2	GRCh38.p7	9:122883261	AATACTTGTTTTTGA[C/T]GCCTGAGGAAATCTT	54542
rs770504214	snp	A/G	1.68042e-05	0.00289859	intron-variant	RC3H2	GRCh38.p7	9:122854653	AATGGTCAAAAAAGT[A/G]AAAAATCAGTGTACT	54542
rs770523822	snp	A/C/G	5.13196e-05	0.00506533	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880797	CTCTTTTGGTAACCT[A/C/G]AAAAATAGAAAAGAG	54542
rs770561203	snp	A/G	3.32784e-05	0.00407898	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880582	AACATCAGCATCTCT[A/G]ATTTCACAAACCTTA	54542
rs770561423	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122894534	TACAAATTTAATTAG[A/G]GTGGTCAGGATTGGC	54542
rs770616895	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122893469	AGTGCACTCCAGTCT[A/G]GGTGACAGAGTGAGA	54542
rs770667900	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122882365	CACATTTCTATTATC[A/C]ACTACCTGTTATCTC	54542
rs770671620	in-del	-/TTTGT			intron-variant	RC3H2	GRCh38.p7	9:122878163	CCTAGGATGAAAACA[-/TTTGT]TTTTAATATTTTAAG	54542
rs770682392	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122870636	TTGCCTAGACTGCCT[G/T]AAATCCTAAATGCAA	54542
rs770702299	snp	C/T	1.67733e-05	0.00289592	synonymous-codon	RC3H2	GRCh38.p7	9:122855206	ACTGATGGGCTTAGT[C/T]GCACTTCCTTGGGAA	54542
rs770722836	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881246	AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGC	54542
rs770725285	in-del	-/CAAA	1.65773e-05	0.00287895	intron-variant	RC3H2	GRCh38.p7	9:122851285	TTATAAATTTTCAAT[-/CAAA]CAAAGCCTCTCAATT	54542
rs770728710	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886866	CCACTTTTAAGTTAG[A/G]TTGTATTTTTGTTTC	54542
rs770753657	snp	C/T	4.50288e-05	0.00474472	intron-variant	RC3H2	GRCh38.p7	9:122849861	AAAACAAATTAGCTT[C/T]AAGTGCAAACTGTTA	54542
rs770766467	snp	C/G	1.65638e-05	0.00287778	missense	RC3H2	GRCh38.p7	9:122858036	GGTACTGTGCCCACT[C/G]ATCTGGCTTTCTTCT	54542
rs770768410	snp	A/C/T	3.31275e-05	0.00406975	missense	RC3H2	GRCh38.p7	9:122865592	ACAGTGTTGTTTACA[A/C/T]CAACTTTATTTAGAA	54542
rs770823604	snp	A/G	1.66871e-05	0.00288847	intron-variant	RC3H2	GRCh38.p7	9:122858108	CCTAATGGGGGATAA[A/G]AGAAACAATCTTAAT	54542
rs770831140	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876236	GCTAAACTGGGTACA[C/T]GAGGTGAGTACAATG	54542
rs770846434	snp	A/G	3.33578e-05	0.00408384	synonymous-codon	RC3H2	GRCh38.p7	9:122854221	AAGGTCCCCAGTACT[A/G]GAATGCTTTCTATGA	54542
rs770918855	snp	A/G	3.31565e-05	0.0040715	intron-variant	RC3H2	GRCh38.p7	9:122854093	GCTCTTGGCCTATAT[A/G]AGGAGGGAAAAAAAG	54542
rs770931519	snp	A/G	1.6593e-05	0.00288031	intron-variant	RC3H2	GRCh38.p7	9:122892870	GTAAATGTACTACCA[A/G]GTCCTACTTATCAGT	54542
rs770936968	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906470	CGGGAGACGGAGGTT[A/G]CAGTGAGCCGAGACC	54542
rs770959243	snp	C/T	1.65844e-05	0.00287957	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879982	AAGCAACTGAGCATA[C/T]TCCCACATACCTGGA	54542
rs771010576	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122875442	GTTTTTATAAATAAA[A/G]TTTACAGCCATGCCC	54542
rs771017442	snp	A/T	1.65985e-05	0.00288079	missense	RC3H2	GRCh38.p7	9:122892994	TTTATTCTCACCTAG[A/T]TTACTTAACTTAATT	54542
rs771032610	snp	G/T	1.65641e-05	0.00287781	missense	RC3H2	GRCh38.p7	9:122859919	TAAAATTACTCACCT[G/T]TCTGTGGGTACTGTG	54542
rs771042904	in-del	-/CAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870405	AAACAAACAAACAAA[-/CAAACAAAC]AAAAAAAAAACAACA	54542
rs771121077	in-del	-/TACTT			intron-variant	RC3H2	GRCh38.p7	9:122885179	TTTAGGAAAACTAAA[-/TACTT]TAGTTTTAAAGTATT	54542
rs771150181	in-del	-/CAGATCATT	1.6591e-05	0.00288015	cds-indel	RC3H2	GRCh38.p7	9:122897543	GGGTTAGCAGTCTAG[-/CAGATCATT]ATTTTGCTGTGTAGT	54542
rs771170899	snp	C/T	5.04503e-05	0.00502221	intron-variant	RC3H2	GRCh38.p7	9:122855689	ATGAGTGAACATGCA[C/T]CATCTCTCACCTCCA	54542
rs771184274	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122891023	CCCCATTTTTTTTTT[-/TT]TTTTTTTTTTTTGGA	54542
rs771213193	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122860003	GAATGCGGAGGATAT[A/G]CTGGTACTCTAGTTA	54542
rs771221268	in-del	-/CA			intron-variant	RC3H2	GRCh38.p7	9:122875247	CTGCTCTTTTCACTG[-/CA]CACACACTTATCTTC	54542
rs771268655	snp	A/G	1.6582e-05	0.00287936	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880115	TTTGCAAATGACTCT[A/G]GAGACTGTAGCTAAC	54542
rs771336070	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857717	AAAGATTTTGAATTC[C/T]TAGTAAAGGACTATG	54542
rs771349295	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122888625	ACTTACCAACGTATC[C/T]GGAGGTCACACCCTA	54542
rs771362338	snp	C/T	1.65625e-05	0.00287766	synonymous-codon	RC3H2	GRCh38.p7	9:122883318	TACCAGAACTTTCCT[C/T]GAGAGGGCAGAACCA	54542
rs771432769	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122903645	ATAGAACAAGTGCCT[A/G]TTTGAATTATAACAT	54542
rs771454429	snp	C/T			synonymous-codon	RC3H2	GRCh38.p7	9:122897369	AAAAGGACAAGCTTT[C/T]CGATGAAGTTTATTC	54542
rs771473617	snp	C/T	1.65985e-05	0.00288079	missense	RC3H2	GRCh38.p7	9:122851423	GTTGCATCTTCTGTA[C/T]AATCACTCTGTAACT	54542
rs771477959	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122882511	CTTTCATAGAAGCCA[A/C]TAGGCCTTTCTATTT	54542
rs771529294	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122896454	ATATAAAAATATTTC[G/T]TATCCACCAATATCA	54542
rs771544174	snp	A/G	1.65877e-05	0.00287986	intron-variant	RC3H2	GRCh38.p7	9:122855420	AACCAAAGAAAATCA[A/G]TAAAAGGACTGTTGG	54542
rs771557971	in-del	-/AAGT			intron-variant	RC3H2	GRCh38.p7	9:122873332	CTGGTTGGAAATAAG[-/AAGT]AAGAACTGTATATTA	54542
rs771565042	snp	C/T	0.000138552	0.00832207	intron-variant	RC3H2	GRCh38.p7	9:122875389	TAAGATAGACAAACA[C/T]TTAATAAACAGATCA	54542
rs771634447	in-del	-/A	1.6799e-05	0.00289814	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880212	ATCAACATATTTAAT[-/A]ACGTTTTCAAGTGTC	54542
rs771646614	snp	A/T	1.65864e-05	0.00287974	intron-variant	RC3H2	GRCh38.p7	9:122851034	CATTTTTTTCTCTTT[A/T]TTATGTCCTATGCCC	54542
rs771652565	snp	C/G	1.79683e-05	0.00299731	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880821	AAAAGAGAAAAATCA[C/G]AATTGGTCTGTGCTT	54542
rs771672692	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122875850	GGCAGACACAGATTA[A/G]ATGATGCAGGGTCTT	54542
rs771678059	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122852857	GGAGCCCCTCTGCCC[A/G]GCCACCACCCCGTCT	54542
rs771741495	snp	A/G	0.000187054	0.00966913	intron-variant	RC3H2	GRCh38.p7	9:122858139	CATCTAGGGAGTGGT[A/G]AATAAATTTAACTGT	54542
rs771767074	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122883545	ATTTAAAAAGTAATC[A/G]AGCAAAATAAAACAT	54542
rs771840911	snp	C/T	1.65625e-05	0.00287766	missense	RC3H2	GRCh38.p7	9:122851130	TCTGCTTTGGTGGCT[C/T]CTTTTGGTGCTGCTG	54542
rs771871309	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122873857	GAATCTTGCTCTGTC[A/G]TCCACACAGGAGTAT	54542
rs771958025	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122855960	TAAAGTAACTATTAT[A/C]GAATTCAGAGGACTT	54542
rs771962602	in-del	-/T	1.65625e-05	0.00287766	frameshift-variant	RC3H2	GRCh38.p7	9:122851107	TCTTCACCTAAACTC[-/T]TGTTTCTTCTGCTTT	54542
rs771987822	snp	A/T	1.70548e-05	0.00292012	intron-variant	RC3H2	GRCh38.p7	9:122897265	CAACCTATAGTAAAA[A/T]CTTGAATGCTTACCT	54542
rs772007714	snp	C/T	0.000153908	0.00877099	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849616	CACAAATTTGAAAGA[C/T]GAACCTCCTTTCAGC	54542
rs772075817	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122894919	GGAGACAGACTGAAC[G/T]TTCTAGGCAAAGGTA	54542
rs772078357	snp	C/T	1.65842e-05	0.00287955	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880021	TATGTTTGCAAGAAG[C/T]TCTAAATGAGGCCTC	54542
rs772099329	in-del	-/AAACAAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870378	AGACTCTGTCTCCAA[-/AAACAAACAAACAAAC]AAACAAACAAACAAA	54542
rs772108418	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122856186	CACCAAGAAAAAAAA[A/C]AGTAAGAGAAAACAA	54542
rs772119324	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122884962	TTCCAGAATAAAGAC[A/G]ACTAAAAAGAGACAT	54542
rs772119457	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122850895	AAAAAGCAAGTTTCA[C/G]GCTACCAAAATGGAC	54542
rs772152294	in-del	-/ACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870404	CAAACAAACAAACAA[-/ACAAACAAAC]AAAAAAAAAACAACA	54542
rs772152675	snp	C/T	6.67579e-05	0.00577707	missense	RC3H2	GRCh38.p7	9:122855841	TAATGGGAAAGATGA[C/T]CTTCTTCAAATTTTG	54542
rs772161628	snp	G/T			missense	RC3H2	GRCh38.p7	9:122858741	ATATCCATCTAATGA[G/T]TTATATCTTTCCCGC	54542
rs772168238	snp	C/G	1.65781e-05	0.00287902	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880147	AACAGAAATGAGAAT[C/G]CTTTTTACTTTGGTT	54542
rs772207471	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882318	AGCTAGTGTCCAAGC[C/T]TCATTAGTGGAGTTA	54542
rs772218695	in-del	-/A	0.001722	0.0292922	intron-variant	RC3H2	GRCh38.p7	9:122855885	CTCTGAGAACTGGTT[-/A]AAAAAAAATAAATAA	54542
rs772240852	snp	C/T			missense	RC3H2	GRCh38.p7	9:122860036	AATGGGCTGGATTTT[C/T]GAGGCACAGAATTCA	54542
rs772251800	in-del	-/AAATT	1.66751e-05	0.00288744	intron-variant	RC3H2	GRCh38.p7	9:122877433	TCCCATAAAAATCAA[-/AAATT]AAACCCATATGAAAC	54542
rs772268566	in-del	-/TTTTTTTTTTT			intron-variant	RC3H2	GRCh38.p7	9:122859256	TATACCCTGGCTTTT[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT	54542
rs772290208	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122900016	TTCAACCATACAGAA[A/G]AATGCTATCTTTCAT	54542
rs772307332	snp	C/T	0.000115028	0.00758294	intron-variant	RC3H2	GRCh38.p7	9:122890220	TTGTACATATAAAGA[C/T]GGGTTGAGTCTCAGG	54542
rs772309904	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122904915	TCCGCATCGAAAAAG[C/T]CCTACCAGAGAGAGG	54542
rs772333798	snp	A/G	6.62405e-05	0.00575464	synonymous-codon	RC3H2	GRCh38.p7	9:122860029	AGTTAGAAATGGGCT[A/G]GATTTTTGAGGCACA	54542
rs772359658	snp	A/C/G	3.4194e-05	0.00413474	intron-variant	RC3H2	GRCh38.p7	9:122857893	GTTTGACCTATCCCT[A/C/G]CAACATTAAGTAATT	54542
rs772391828	snp	A/G	1.66327e-05	0.00288376	intron-variant	RC3H2	GRCh38.p7	9:122860142	TTTTACTGGAGAGAA[A/G]ATTTAACAAAGGGCA	54542
rs772410976	snp	C/G/T	3.39491e-05	0.0041199	intron-variant	RC3H2	GRCh38.p7	9:122851449	TAACTAAGAAAAATA[C/G/T]TGATTTTGCTCTCCC	54542
rs772423365	snp	C/T			missense	RC3H2	GRCh38.p7	9:122890348	CTCGAGCCCTGACAG[C/T]GGCCCATAGATTGGC	54542
rs772446546	snp	C/T	3.3162e-05	0.00407184	intron-variant	RC3H2	GRCh38.p7	9:122877605	AAATGGGAACACATT[C/T]AATGAGTGGCAAGGT	54542
rs772551470	snp	A/G	1.6646e-05	0.00288491	intron-variant	RC3H2	GRCh38.p7	9:122877446	AAAAATTAAACCCAT[A/G]TGAAACAGAATTCTC	54542
rs772565624	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861357	TAGCCGGGTGTGGTG[A/G]TCCATGCCTGTAATC	54542
rs772582194	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122877091	TATGTTTTGTTGTGA[G/T]GCAGAGTCTTGCTGT	54542
rs772618734	in-del	-/AACT			intron-variant	RC3H2	GRCh38.p7	9:122895083	GGCAATTTAAGAACC[-/AACT]GAGATAACATTTACA	54542
rs772645446	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892515	CTCCCGGGTTCACGC[C/T]ATTCTCCTGCCTCAG	54542
rs772692822	snp	A/C	1.65699e-05	0.00287831	missense	RC3H2	GRCh38.p7	9:122897328	ACAGGAAGTACATCA[A/C]TATCTGTGTTGATGG	54542
rs772699663	snp	C/T	1.66117e-05	0.00288194	missense	RC3H2	GRCh38.p7	9:122849687	GTTTTTATCTTCAGA[C/T]ATAACATGAGTTTTC	54542
rs772733364	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122877464	AAACAGAATTCTCAA[C/G]ACTTACTTTTCAAGC	54542
rs772799157	snp	C/T	1.79078e-05	0.00299226	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880294	ATCTGCCCTATGAAA[C/T]TCATCATTAGACACT	54542
rs772844371	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122870709	GTGTGCACCACCATG[C/G]GTAACTCTCCCTATT	54542
rs772865526	snp	A/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906437	TCGGGGGGCTGAGGC[A/T]GGAGAATCACTTGAA	54542
rs772896304	snp	A/G	1.6574e-05	0.00287867	synonymous-codon	RC3H2	GRCh38.p7	9:122854557	GTGTGCTGATGATGT[A/G]GCCTCGTTGCCATAT	54542
rs772920990	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122869326	TATATATAAACATAT[G/T]GTAATTAAATATAAA	54542
rs772926753	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886142	TTATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	54542
rs772959870	snp	C/G/T	0.000134089	0.00818715	intron-variant	RC3H2	GRCh38.p7	9:122854644	GAATGAAACAATGGT[C/G/T]AAAAAAGTGAAAAAT	54542
rs772990427	snp	C/T	1.6661e-05	0.00288621	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880577	GATAGAACATCAGCA[C/T]CTCTAATTTCACAAA	54542
rs773008821	snp	A/C/G	6.62431e-05	0.00575481	missense	RC3H2	GRCh38.p7	9:122865458	TACTGTCAGTACTAC[A/C/G]TGAGATTAGCTGGGA	54542
rs773059378	snp	A/G	0.000143521	0.00846994	intron-variant	RC3H2	GRCh38.p7	9:122865312	ATTTCTAAAAAGGAA[A/G]AAGAATTTCCAGTAA	54542
rs773071049	snp	C/T	1.65622e-05	0.00287764	missense	RC3H2	GRCh38.p7	9:122890444	GAGCTGCTCGCATGG[C/T]TCTTACACGACCTTC	54542
rs773074615	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122901970	GTTTCGCTCTTGTTG[C/T]CCAGGCTGTAGTGCA	54542
rs773150623	snp	G/T	1.65649e-05	0.00287788	missense	RC3H2	GRCh38.p7	9:122853960	TCTTTACCTCTCCAT[G/T]TCTTAGTTCAATTTC	54542
rs773153946	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122870475	AGCAAAAAATAAAGT[C/T]TTAACTATGAACCTC	54542
rs773158869	snp	G/T	1.65999e-05	0.00288091	intron-variant	RC3H2	GRCh38.p7	9:122877632	AGGTGAAGATTCCAT[G/T]TGTTATTCACTCTAG	54542
rs773227534	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122850902	AAGTTTCAGGCTACC[A/G]AAATGGACTGCTTTG	54542
rs773251074	in-del	-/CCCCGTCCGGGAGGGAGGTGGGGGGGTCAGCCCCCCGCCCAGCCAGCCG			intron-variant	RC3H2	GRCh38.p7	9:122867874	TCCGCCCGGCAGCCA[lengthTooLong]CCCCGTCCGGGAGGG	54542
rs773275477	snp	A/C			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905319	CCACCTCCGCCTCCT[A/C]CTCCTCCTCCTCCTC	54542
rs773276161	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122882628	GTATCTGTCACTACC[C/G]GCTAGACTATTAGAC	54542
rs773313548	in-del	-/CAAACAA			intron-variant	RC3H2	GRCh38.p7	9:122870397	AAACAAACAAACAAA[-/CAAACAA]ACAAACAAACAAAAA	54542
rs773333608	snp	A/G	1.85775e-05	0.00304769	intron-variant	RC3H2	GRCh38.p7	9:122890586	GCTAAAGTTTTTTCA[A/G]TAAAAAATAAAAGTC	54542
rs773352064	snp	G/T	1.65957e-05	0.00288055	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879837	TTAACAGCTACCATT[G/T]CATTTTCCAGCTGCT	54542
rs773355030	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122874165	AAACAATATAGACAA[C/G]TGAAAAGAAGAGTAA	54542
rs773358666	snp	A/G	0.000167953	0.00916232	missense	RC3H2	GRCh38.p7	9:122859081	ACACCAGCTGGTACC[A/G]TTGGAGGTGGTGGAT	54542
rs773444649	in-del	-/CAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870389	CCAAAAACAAACAAA[-/CAAACAAAC]AAACAAACAAACAAA	54542
rs773487759	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122872695	GTTCACGCGATTCTC[A/G]TGCCTCAGCCTCCCC	54542
rs773492356	snp	C/T	8.28796e-05	0.00643684	intron-variant	RC3H2	GRCh38.p7	9:122851048	TATTATGTCCTATGC[C/T]CACTGTTTATGAATT	54542
rs773556826	snp	C/T	1.65699e-05	0.00287831	missense	RC3H2	GRCh38.p7	9:122855261	GTATGGTAACCTGTA[C/T]GGGAAGATCTGGAAA	54542
rs773556912	snp	C/T	1.65693e-05	0.00287826	intron-variant	RC3H2	GRCh38.p7	9:122859904	TTTCTTAGAATTGTC[C/T]AAAATTACTCACCTG	54542
rs773564058	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122901753	CGCACCACCATGCCC[A/G]GTTAATTTTTGTATT	54542
rs773646893	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122863742	AGATTGTAAAAGTCC[-/T]TTTTTTTTTTTGAGA	54542
rs773695534	snp	A/C			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881204	CAAAGAAAGGTGAGG[A/C]GGCCAGGGATGGTGG	54542
rs773714779	snp	A/C	3.82453e-05	0.00437278	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880842	GTCTGTGCTTTCTCC[A/C]TTCAACTGATTCGTT	54542
rs773734366	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122887157	AAGCCCATTAATACA[A/T]TTGGGGATGTAAAAT	54542
rs773798867	snp	C/T	1.66045e-05	0.00288132	missense	RC3H2	GRCh38.p7	9:122865635	TTACAGTGGCATTGA[C/T]CTTTTTGTTCCTTAA	54542
rs773802890	snp	A/G	1.65616e-05	0.00287759	missense	RC3H2	GRCh38.p7	9:122883278	CCTGAGGAAATCTTG[A/G]TTCTAGTCTCTGCAC	54542
rs773933036	snp	C/T	1.65614e-05	0.00287757	missense	RC3H2	GRCh38.p7	9:122865479	TTAGCTGGGAAACAC[C/T]GTTTTCTGCATTTGA	54542
rs773933331	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881398	GGGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATAG	54542
rs773971464	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122894701	CCTGGCCAATATGGC[A/G]AGACCCCATCTCTAC	54542
rs773992364	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122901002	AGGCATCTCTTATAT[G/T]ATTCAAATTACAAAC	54542
rs774061598	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122879709	ATGTTCAGGATGAAA[C/G]TGAGTTAGAGACAAC	54542
rs774094601	snp	A/G	4.80411e-05	0.00490084	intron-variant	RC3H2	GRCh38.p7	9:122849868	ATTAGCTTTAAGTGC[A/G]AACTGTTAAGGGTGA	54542
rs774150613	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122850832	ATTTGGCAACCAGAT[G/T]AAAGAAGCATAACCT	54542
rs774168336	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122862438	TTCTCCATCCACAAG[A/G]CCCTTCCTTCCTTGC	54542
rs774226375	in-del	-/TTTT			intron-variant	RC3H2	GRCh38.p7	9:122860406	ACCATTTACCCATTC[-/TTTT]TTTTTTTTTTTTTTT	54542
rs774251671	snp	A/G	4.96931e-05	0.00498439	missense	RC3H2	GRCh38.p7	9:122853971	CCATTTCTTAGTTCA[A/G]TTTCCTTGCTTAAAA	54542
rs774260943	snp	C/T	2.10595e-05	0.00324489	missense	RC3H2	GRCh38.p7	9:122859096	GTTGGAGGTGGTGGA[C/T]AGTATCCTTGAAAAT	54542
rs774340600	in-del	-/TCTCCCTCTCCCTCTCCCTCTCCCCATGG	1.83594e-05	0.00302975	intron-variant	RC3H2	GRCh38.p7	9:122851459	AAATACTGATTTTGC[lengthTooLong]TCTCCCTCTCCCCAT	54542
rs774367405	snp	A/G/T	3.31209e-05	0.00406935	missense	RC3H2	GRCh38.p7	9:122860006	TGCGGAGGATATACT[A/G/T]GTACTCTAGTTAGAA	54542
rs774401546	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122893477	CCAGTCTGGGTGACA[C/G]AGTGAGACTCCATCT	54542
rs774454334	in-del	-/TTT			intron-variant	RC3H2	GRCh38.p7	9:122859254	CTTTATACCCTGGCT[-/TTT]TTTTTTTTTTTTTTT	54542
rs774482826	in-del	-/TCT	0.00028361	0.0119048	cds-indel	RC3H2	GRCh38.p7	9:122855841	TAATGGGAAAGATGA[-/TCT]TCTTCAAATTTTGTA	54542
rs774483373	snp	C/T	3.3211e-05	0.00407485	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879871	AAGTTGGTGAAACAG[C/T]GTCTAAAATAAGCCA	54542
rs774483446	snp	C/T	1.66001e-05	0.00288094	missense	RC3H2	GRCh38.p7	9:122892995	TTATTCTCACCTAGA[C/T]TACTTAACTTAATTG	54542
rs774509128	snp	A/G	1.65627e-05	0.00287769	stop-gained	RC3H2	GRCh38.p7	9:122859923	ATTACTCACCTGTCT[A/G]TGGGTACTGTGGGAC	54542
rs774514140	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122857726	GAATTCTTAGTAAAG[A/G]ACTATGCCTTAACGG	54542
rs774562157	snp	C/T	1.67511e-05	0.00289401	intron-variant	RC3H2	GRCh38.p7	9:122855702	CATCATCTCTCACCT[C/T]CAACCCCTGCAACCC	54542
rs774571021	snp	A/T	1.65647e-05	0.00287786	missense	RC3H2	GRCh38.p7	9:122883334	GAGAGGGCAGAACCA[A/T]CTTCTAATGCCAGTA	54542
rs774571302	snp	C/T	1.65853e-05	0.00287964	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880011	GATTAGGGTCTATGT[C/T]TGCAAGAAGCTCTAA	54542
rs774605549	snp	A/C	0.000109176	0.00738757	intron-variant	RC3H2	GRCh38.p7	9:122875193	CCTCTTCTCTAGGCA[A/C]TTCAAGTGGGGAAAA	54542
rs774684275	snp	C/T	3.31252e-05	0.00406958	missense	RC3H2	GRCh38.p7	9:122851162	ACTGGATGCCCATTT[C/T]CCACTGCCATTCCAT	54542
rs774715016	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122902131	AGATGGGGTTTATCC[A/G]TGTTGGTCAGGCTGG	54542
rs774733515	snp	C/T	0.00018225	0.00954421	intron-variant	RC3H2	GRCh38.p7	9:122851310	CTCTCAATTATCTAA[C/T]TGTGGCACTTACTTC	54542
rs774740096	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122888703	TACACTGGAAGGATA[C/T]ACCACAGTTTATTAT	54542
rs774742660	in-del	-/AAGC			intron-variant	RC3H2	GRCh38.p7	9:122885787	AAACTCATCACCATT[-/AAGC]AAGCAGTCACTGTTC	54542
rs774770901	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889681	CAAAAAAAAAGCTTA[C/T]CTTTCTTTGGCTTAT	54542
rs774786958	snp	C/T	3.47935e-05	0.0041708	intron-variant	RC3H2	GRCh38.p7	9:122890214	CAAGATTTGTACATA[C/T]AAAGACGGGTTGAGT	54542
rs774826321	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122879535	GGTCAAAAATATTCT[A/G]CAATAAAGTATACTC	54542
rs774885339	snp	C/T	1.65745e-05	0.00287871	synonymous-codon	RC3H2	GRCh38.p7	9:122865618	TAGAAGAGGAAACGT[C/T]CTTACAGTGGCATTG	54542
rs774897231	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122874373	AAAGACAGATTGAGA[G/T]ATAGGAAGATACTGG	54542
rs774930533	snp	A/G	1.65625e-05	0.00287766	synonymous-codon	RC3H2	GRCh38.p7	9:122851137	TGGTGGCTCCTTTTG[A/G]TGCTGCTGTACTGGA	54542
rs774940647	snp	A/T	1.70029e-05	0.00291568	intron-variant	RC3H2	GRCh38.p7	9:122858140	ATCTAGGGAGTGGTG[A/T]ATAAATTTAACTGTG	54542
rs774965084	in-del	-/TC	1.65754e-05	0.00287879	intron-variant	RC3H2	GRCh38.p7	9:122883155	ATGAATTTCAGGAAG[-/TC]TCTGTCTCACAAACA	54542
rs774967665	in-del	-/CCCTGCTTT			intron-variant	RC3H2	GRCh38.p7	9:122859224	TTGAACCTTACCTTA[-/CCCTGCTTT]ATAAAGCTTTATACC	54542
rs775017843	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122902328	TCAAATCATAGCCAA[G/T]GGATAACTTCATCCT	54542
rs775096311	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122895005	CTAAGAAGCCAGTGT[A/G]GCTTAAGCAGAATAA	54542
rs775122099	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122882525	AATAGGCCTTTCTAT[G/T]TCCAAGTACATGAGC	54542
rs775124964	in-del	-/TAAATTA			intron-variant	RC3H2	GRCh38.p7	9:122903109	CAACTCTAGAATATT[-/TAAATTA]TAAATTATAAAGTAA	54542
rs775137233	snp	C/G/T	5.41153e-05	0.00520146	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880824	AGAGAAAAATCAGAA[C/G/T]TGGTCTGTGCTTTCT	54542
rs775155151	snp	C/T	3.40779e-05	0.00412769	intron-variant	RC3H2	GRCh38.p7	9:122897266	AACCTATAGTAAAAT[C/T]TTGAATGCTTACCTG	54542
rs775218620	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122873887	TAGTGGCGCCATCTC[A/G]GCTCACTGCAACCTC	54542
rs775259572	snp	A/G			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881611	CCATTATATACTACG[A/G]CAGGGAATTTGGATA	54542
rs775343633	snp	C/T	1.66244e-05	0.00288304	missense	RC3H2	GRCh38.p7	9:122858697	ACAGTTGTCCTTGGC[C/T]CACTTGGTGGCTGAC	54542
rs775393227	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884277	CAGCCTCAGCAACAA[C/T]GCGAGACTCCGTCTC	54542
rs775427008	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122854883	CTGAGGCGGGTGGAT[A/C]ACATGAGGCCAGGAG	54542
rs775444717	in-del	-/TA			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906926	CCACCCTACTGTGTA[-/TA]TATATATATATACAC	54542
rs775466185	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122896464	ATTTCTTATCCACCA[A/G]TATCACTTATATACA	54542
rs775499402	snp	C/T	3.31559e-05	0.00407147	missense	RC3H2	GRCh38.p7	9:122858986	ATGTACTGTAATGAT[C/T]GGCATATGGCATGGA	54542
rs775508072	snp	C/T	3.31208e-05	0.00406931	missense	RC3H2	GRCh38.p7	9:122859948	TGGGACTTCAAAGGG[C/T]ATCTGAGTCCTTGGA	54542
rs775512492	in-del	-/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905855	TTAAAGAGAAAACTC[-/T]TGTTTCTAGACAAAG	54542
rs775543477	in-del	-/AAGTC			intron-variant	RC3H2	GRCh38.p7	9:122858314	TTTTCTTGCTTAGGG[-/AAGTC]ATTTGTATGTATGTG	54542
rs775581799	snp	C/T	8.34202e-05	0.0064578	synonymous-codon	RC3H2	GRCh38.p7	9:122883372	CTTCAAGGCCTCTTC[C/T]TGCATAGCTAAAAAT	54542
rs775706323	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122860030	GTTAGAAATGGGCTG[A/G]ATTTTTGAGGCACAG	54542
rs775737990	snp	A/G	1.65674e-05	0.00287809	missense	RC3H2	GRCh38.p7	9:122851331	CACTTACTTCAATTG[A/G]TTCACTTTGTCCATC	54542
rs775738629	snp	C/T	3.31203e-05	0.00406928	missense	RC3H2	GRCh38.p7	9:122858847	TGGTACATAGGTGGG[C/T]GCCAGATGCGCCTGC	54542
rs775739449	snp	C/T	0.000104685	0.00723404	intron-variant	RC3H2	GRCh38.p7	9:122890224	ACATATAAAGACGGG[C/T]TGAGTCTCAGGATTC	54542
rs775792445	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122891433	GTAGATCACTACAAT[G/T]GATCTGTTCACTACT	54542
rs775865546	snp	A/G			synonymous-codon	RC3H2	GRCh38.p7	9:122858825	GCTTCTAATAATGTC[A/G]TCTCGTTGGTACATA	54542
rs775938127	snp	A/G	1.65806e-05	0.00287924	intron-variant	RC3H2	GRCh38.p7	9:122877607	ATGGGAACACATTCA[A/G]TGAGTGGCAAGGTGA	54542
rs775996433	in-del	-/TG			intron-variant	RC3H2	GRCh38.p7	9:122878825	GCGATCTCGGCTCAC[-/TG]TAGCCTCCATCTCCC	54542
rs775999367	snp	A/C	1.65658e-05	0.00287795	missense	RC3H2	GRCh38.p7	9:122858957	AGAAGAATTCATTCG[A/C]TCTCGAGGGGAAAAT	54542
rs776044453	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857782	CGTAGTGCATTTATA[C/T]TCAGTGTTTATTGAA	54542
rs776050212	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892632	TAGCCAGGATAGTCT[C/T]GATCTTCTGATCTTG	54542
rs776053116	in-del	-/AACC			intron-variant	RC3H2	GRCh38.p7	9:122895263	TCCTGGGCTCAAGTG[-/AACC]AACCTCCCATCTCAC	54542
rs776057339	snp	C/T	1.65844e-05	0.00287957	missense	RC3H2	GRCh38.p7	9:122858712	TCACTTGGTGGCTGA[C/T]AAGCCACCGAATAAT	54542
rs776108258	snp	C/T	3.34784e-05	0.00409122	missense	RC3H2	GRCh38.p7	9:122854261	TCAGTAACAATGAAT[C/T]TGTCCCTTTAAAGAG	54542
rs776114386	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892040	GACTTATCAAAACTA[A/G]TATTCTGTTACAGCA	54542
rs776146697	snp	G/T			utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849483	AGAGGGCTTGAAGTA[G/T]CAAAGAGTCCACAGG	54542
rs776148284	snp	A/T	1.72279e-05	0.0029349	intron-variant	RC3H2	GRCh38.p7	9:122893034	TCTGGTACCTTAAAA[A/T]AAAAAAAAAAGGAAT	54542
rs776156797	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122890603	AAAAAATAAAAGTCA[A/G]TTTTCATTATCTGCA	54542
rs776158104	in-del	-/CAAT			intron-variant	RC3H2	GRCh38.p7	9:122870985	TCATTTTCCCATCTC[-/CAAT]AGCCTTTTCCCTTCC	54542
rs776275438	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122865696	TTGGTGAATATTTCA[C/T]TAAATCTTACTCAAG	54542
rs776279205	snp	C/T	0.000355682	0.013331	intron-variant	RC3H2	GRCh38.p7	9:122875184	CTCCTTAATCCTCTT[C/T]TCTAGGCACTTCAAG	54542
rs776310057	snp	G/T	1.65603e-05	0.00287747	synonymous-codon	RC3H2	GRCh38.p7	9:122858815	GTAAAGAATTGCTTC[G/T]AATAATGTCATCTCG	54542
rs776313372	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122860408	CATTTACCCATTCTT[-/TT]TTTTTTTTTTTTTTT	54542
rs776366560	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122882629	TATCTGTCACTACCC[A/G]CTAGACTATTAGACA	54542
rs776367402	snp	A/G	1.66621e-05	0.00288631	intron-variant	RC3H2	GRCh38.p7	9:122860162	AACAAAGGGCAAAGG[A/G]GAAATCACTGTCTAT	54542
rs776368274	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122897701	TTTTATAACCTTTGG[A/G]TGTCTTTTTTAAAAA	54542
rs776422056	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122896601	AATCAGGTACATTGA[A/T]ATTTATTTTTTACAC	54542
rs776424621	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905446	GGAAGGAAAGCGTAG[C/T]AGCCCCAGCCACCCA	54542
rs776456467	in-del	-/CAAACAA			intron-variant	RC3H2	GRCh38.p7	9:122870401	AAACAAACAAACAAA[-/CAAACAA]ACAAACAAAAAAAAA	54542
rs776481189	snp	A/G	3.32651e-05	0.00407817	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880184	ACACATTTATACTCA[A/G]ATACTTTCAATTTAT	54542
rs776509817	snp	A/G	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122860039	GGGCTGGATTTTTGA[A/G]GCACAGAATTCAGCT	54542
rs776523802	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122883893	CAGCTACTTTGGAGG[C/T]GGAAGTGGAGGATCA	54542
rs776561030	snp	C/T	0.000523457	0.0161696	intron-variant	RC3H2	GRCh38.p7	9:122890248	AGGATTCACCGAGCT[C/T]CAGAAATTGGCATCC	54542
rs776566134	in-del	-/TCTCCCTCTCCCCATGG	0.00264745	0.0362866	intron-variant	RC3H2	GRCh38.p7	9:122851471	TGCTCTCCCTCTCCC[-/TCTCCCTCTCCCCATGG]TCTCCCTCTCCCCAT	54542
rs776644018	snp	A/T	1.9303e-05	0.00310662	intron-variant	RC3H2	GRCh38.p7	9:122855885	CTCTGAGAACTGGTT[A/T]AAAAAAAATAAATAA	54542
rs776716532	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122856497	TGGGCTCAAGCAATC[C/T]ACCCACTTCGATCTT	54542
rs776719662	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122858330	AGTCATTTGTATGTA[G/T]GTGGTGATACTGAAA	54542
rs776785266	snp	C/G	1.65831e-05	0.00287945	intron-variant	RC3H2	GRCh38.p7	9:122877613	ACACATTCAATGAGT[C/G]GCAAGGTGAAGATTC	54542
rs776809154	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122887130	TTTAACAGCCACAAA[C/T]AATTCTTGCTGAAGC	54542
rs776832225	snp	A/G			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122906689	GTTTTAACAAAATAT[A/G]TAGTTATTACCTATT	54542
rs776891338	snp	C/T	3.71955e-05	0.00431235	intron-variant	RC3H2	GRCh38.p7	9:122851476	TCCCTCTCCCTCTCC[C/T]TCTCCCCATGGTCTC	54542
rs776918671	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122859148	TAATCTTAGTACAAT[A/C]CAACATTTTATAATG	54542
rs776944597	snp	A/C	4.96964e-05	0.00498455	intron-variant, missense	RC3H2	GRCh38.p7	9:122853941	GAAGCCGAAAGGTTC[A/C]GTTTCTTTACCTCTC	54542
rs776947644	snp	A/G/T	3.31885e-05	0.0040735	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879827	AACTACTGTTTTAAC[A/G/T]GCTACCATTGCATTT	54542
rs776976109	snp	C/T	1.65732e-05	0.00287859	missense	RC3H2	GRCh38.p7	9:122858976	CGAGGGGAAAATGTA[C/T]TGTAATGATCGGCAT	54542
rs776991774	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122879280	TTGCCTGTAATCCCA[A/G]TTACTTGGGAGGCTG	54542
rs777018294	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122882868	TTACATACTCCTTAT[A/G]AAGTTTCCAATATAG	54542
rs777119577	snp	A/G	1.65773e-05	0.00287895	intron-variant	RC3H2	GRCh38.p7	9:122877602	CAAAAATGGGAACAC[A/G]TTCAATGAGTGGCAA	54542
rs777147794	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122860916	CTTGAGGAAAGGCCA[C/T]TTTTGTTTATTTTGA	54542
rs777157254	snp	A/G	1.65842e-05	0.00287955	synonymous-codon	RC3H2	GRCh38.p7	9:122855245	CTGGACAGGATCTGT[A/G]GTATGGTAACCTGTA	54542
rs777189184	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122887628	AGCATTTTCAGTGGA[C/G]AGACCTTGGACACTG	54542
rs777193919	in-del	-/AATT	1.70426e-05	0.00291908	intron-variant	RC3H2	GRCh38.p7	9:122858143	AGGGAGTGGTGAATA[-/AATT]AATTTAACTGTGTGA	54542
rs777212599	snp	A/G	3.31614e-05	0.00407181	intron-variant	RC3H2	GRCh38.p7	9:122851037	TTTTTTCTCTTTATT[A/G]TGTCCTATGCCCACT	54542
rs777273397	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122899022	TCACATTCAAAGAGA[A/C]AAAATATATAACAGA	54542
rs777283776	in-del	-/ACTTAGAAAACTTAT	3.74553e-05	0.00432738	intron-variant	RC3H2	GRCh38.p7	9:122880307	AATTCATCATTAGAC[-/ACTTAGAAAACTTAT]AAGCTGTATTAACTC	54542
rs777306835	snp	C/G	1.66579e-05	0.00288595	missense	RC3H2	GRCh38.p7	9:122890536	GCACTCTGGTTCAAG[C/G]TAGCTACACCTTTAG	54542
rs777326769	snp	C/T	1.65638e-05	0.00287778	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880640	TGAGCCAAATCACCA[C/T]ACAAAAGAGAGGACC	54542
rs777401348	snp	A/G	1.70284e-05	0.00291786	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879759	AATGTACTTACCTGA[A/G]GGGTCTCATGGCCTT	54542
rs777469914	snp	A/G	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122858923	GTCCATACGGCTGCG[A/G]AGGAGGAGGCTGGTA	54542
rs777522366	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122851310	CTCTCAATTATCTAA[-/T]TGTGGCACTTACTTC	54542
rs777549417	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122894349	ATAGGTACCAGGGAT[A/G]TATCAATGAGCAAAA	54542
rs777557279	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122899916	AGTACAAAATAAGAG[C/T]AAATACCTTTTCCTT	54542
rs777562155	snp	C/T	3.31312e-05	0.00406995	missense, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880742	AATGCTTCATAACTC[C/T]GAAATTCCTCCTTCA	54542
rs777581954	snp	C/T	1.81076e-05	0.0030089	intron-variant	RC3H2	GRCh38.p7	9:122855180	TATTATCTAAATGGA[C/T]TACCTGATACACTGA	54542
rs777588729	snp	A/G	1.66446e-05	0.00288479	intron-variant	RC3H2	GRCh38.p7	9:122860150	GAGAGAAAATTTAAC[A/G]AAGGGCAAAGGAGAA	54542
rs777610455	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122861715	GTTTTTTCCTCAAAT[C/T]AGAACAATCATTTTA	54542
rs777617314	snp	C/T	1.65633e-05	0.00287774	missense	RC3H2	GRCh38.p7	9:122865575	TTCCGGCTGTGGTTG[C/T]GACAGTGTTGTTTAC	54542
rs777622309	in-del	-/A	1.65666e-05	0.00287802	intron-variant	RC3H2	GRCh38.p7	9:122851232	TGTCCAAGATCTCCT[-/A]AGAAAATAAAATGTT	54542
rs777629380	in-del	-/TAC	1.66128e-05	0.00288204	intron-variant	RC3H2	GRCh38.p7	9:122854172	AATTTATAGCTGAGT[-/TAC]TACAGAGCCTACCTG	54542
rs777650223	snp	C/T	4.97022e-05	0.00498484	intron-variant	RC3H2	GRCh38.p7	9:122883186	AGGCATGTCTTTACA[C/T]AGATACTTACTGCTT	54542
rs777652518	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122904654	CCAGGGCATTGTTTG[C/G]CCGGGGTTCCTATTT	54542
rs777711514	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886793	ACTCAGGGTTTTTTC[A/G]TGTGCTTGTTAGTCA	54542
rs777741240	snp	A/G	4.96874e-05	0.0049841	synonymous-codon	RC3H2	GRCh38.p7	9:122851104	ATGGTCTTCACCTAA[A/G]CTCTGTTTCTTCTGC	54542
rs777750839	snp	C/T	1.75823e-05	0.00296493	intron-variant	RC3H2	GRCh38.p7	9:122858650	TTAATGACTACATTA[C/T]AGTAGCATCTTCACT	54542
rs777776300	snp	A/T	1.65619e-05	0.00287762	missense	RC3H2	GRCh38.p7	9:122855340	GATCTTCTTCTTTTG[A/T]CCTTCTCTGGGTTTC	54542
rs777808197	snp	A/G	1.6646e-05	0.00288491	synonymous-codon	RC3H2	GRCh38.p7	9:122854200	CTGCTGAAGTTCAAG[A/G]CTCAAAAGGTCCCCA	54542
rs777815395	snp	A/G	1.70432e-05	0.00291913	intron-variant	RC3H2	GRCh38.p7	9:122865683	AACAATCAACAGATT[A/G]GTGAATATTTCACTA	54542
rs777824009	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849025	AAAGCACTGCACCAC[A/C]CTCCTACATATAATG	54542
rs777845242	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122890075	TGAGCATGGATGTCG[A/C]GGCTGCAGTGAGCCA	54542
rs777883645	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122891295	CTCAAAGTGCTGGAA[C/T]TACAGGCGTGAGCCT	54542
rs777893127	snp	C/G/T	4.99707e-05	0.00499833	intron-variant	RC3H2	GRCh38.p7	9:122858102	AAGGTTCCTAATGGG[C/G/T]GATAAAAGAAACAAT	54542
rs777956862	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122865192	TGCAGAACCAAACTA[C/G]AACTCAAATTTTTTA	54542
rs777970918	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903533	TATATGAACAAAGGA[C/T]GTAAGTCTTCTTACA	54542
rs778025465	snp	A/G	1.69833e-05	0.00291399	missense	RC3H2	GRCh38.p7	9:122849796	CTAAAGCAAGAAGTT[A/G]CCGGCAGAATTGTTT	54542
rs778049018	in-del	-/G	4.99963e-05	0.00499956	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879903	AAGGGCATGGGGGTT[-/G]GGGGGGGAAGAATGT	54542
rs778056932	snp	A/G	1.69304e-05	0.00290945	intron-variant	RC3H2	GRCh38.p7	9:122854304	TGTAATAAAAGTGAA[A/G]TGAATGAAGCAACAA	54542
rs778099340	snp	A/G	1.65806e-05	0.00287924	missense	RC3H2	GRCh38.p7	9:122860106	CTACATTACTTACAG[A/G]AGTCTTGGGTGGAGA	54542
rs778172795	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122863788	GTTGCCCAGGCTGGC[A/G]TACAACGGTGCGATC	54542
rs778173274	snp	C/T	1.65831e-05	0.00287945	missense, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880097	GTCAATTCCTGGACA[C/T]TCTTTGCAAATGACT	54542
rs778209263	snp	A/C	3.32497e-05	0.00407722	synonymous-codon	RC3H2	GRCh38.p7	9:122855813	GCCTATGGTGCCACA[A/C]GACCAGGGAGAATAA	54542
rs778262365	snp	C/T	1.72472e-05	0.00293654	intron-variant	RC3H2	GRCh38.p7	9:122857876	GTAATTTGAAGTCAG[C/T]TGTTTGACCTATCCC	54542
rs778264277	snp	A/T	1.65704e-05	0.00287836	intron-variant	RC3H2	GRCh38.p7	9:122851305	AAAGCCTCTCAATTA[A/T]CTAATTGTGGCACTT	54542
rs778272917	snp	A/G	0.000122078	0.00781178	missense	RC3H2	GRCh38.p7	9:122859058	CAAAGCGAGGAACAC[A/G]GGGAGCCACACCAGC	54542
rs778326359	in-del	-/A	1.65853e-05	0.00287964	intron-variant	RC3H2	GRCh38.p7	9:122851032	GCATTTTTTTCTCTT[-/A]TATTATGTCCTATGC	54542
rs778330024	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122874933	AGGTATGAGAAAGAA[G/T]AAAATGGATTTTCAG	54542
rs778349615	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895584	AATTAAATTAAGATA[C/T]ACTATCAATTGTAGA	54542
rs778375901	snp	C/T	3.31225e-05	0.00406941	synonymous-codon	RC3H2	GRCh38.p7	9:122883228	AGAAGCTCGATACAG[C/T]AGTTGCACAACATGA	54542
rs778384972	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857354	TCCTGGTACACAAAC[C/T]TGTTTGGTAATGCCA	54542
rs778436350	snp	A/G	1.65877e-05	0.00287986	missense	RC3H2	GRCh38.p7	9:122855784	GGCTCTGAATCAATG[A/G]CATTTATACAGGAGC	54542
rs778525152	snp	C/G/T	8.29159e-05	0.00643831	intron-variant	RC3H2	GRCh38.p7	9:122859890	ACAATGTTTCTTTTT[C/G/T]TCTTAGAATTGTCTA	54542
rs778540971	snp	G/T	1.65638e-05	0.00287778	intron-variant	RC3H2	GRCh38.p7	9:122883198	ACATAGATACTTACT[G/T]CTTACCTTAAAACAA	54542
rs778621906	in-del	-/TTTA			intron-variant	RC3H2	GRCh38.p7	9:122873807	AACTATACCATAATT[-/TTTA]TTTATTTATTTATAT	54542
rs778686718	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122882492	TTCAAATTTAAATGT[C/T]TTACTTTCATAGAAG	54542
rs778700739	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122887903	TGCCTGACACCACAC[C/G]TGGCTAATTTTTTCT	54542
rs778728210	snp	A/G	3.44442e-05	0.00414981			GRCh38.p7	9:122865698	GGTGAATATTTCACT[A/G]AATCTTACTCAAGAC	54542
rs778736486	snp	C/T					GRCh38.p7	9:122887359	GTAGGAGCTCCTTCA[C/T]GTTCAACTTTTGTCC	54542
rs778818199	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122884801	GAGGTTGCAGTGAGC[C/T]GAGATTACGCCACTG	54542
rs778853188	in-del	-/AACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870403	ACAAACAAACAAACA[-/AACAAACAAAC]AAAAAAAAAACAACA	54542
rs778896085	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122892720	CCGGCTCTAGCTTGA[A/G]TTCTTAATAACAATA	54542
rs778913688	snp	G/T	1.65696e-05	0.00287828	intron-variant	RC3H2	GRCh38.p7	9:122851244	CCTAAGAAAATAAAA[G/T]GTTAATCCTTCAGTA	54542
rs778919583	snp	A/G	6.67379e-05	0.0057762	missense	RC3H2	GRCh38.p7	9:122854226	CCCCAGTACTGGAAT[A/G]CTTTCTATGACCAGA	54542
rs778929123	snp	C/T	1.70586e-05	0.00292045	intron-variant	RC3H2	GRCh38.p7	9:122854490	TAAGATACATACAAG[C/T]CTGAGAATGGAGAAT	54542
rs778957516	in-del	-/A	0.00021913	0.010465	intron-variant	RC3H2	GRCh38.p7	9:122875205	GCACTTCAAGTGGGG[-/A]AAAAAACTGAGAAGA	54542
rs778984343	snp	C/T	1.76431e-05	0.00297005	utr-variant-3-prime	RC3H2	GRCh38.p7	9:122849608	GGTGTGGTCACAAAT[C/T]TGAAAGATGAACCTC	54542
rs778992992	snp	G/T			intron-variant	RC3H2	GRCh38.p7	9:122876956	CAAATAAGACTGCAA[G/T]TATTTTCATTCTGCA	54542
rs779020490	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905704	GATACATCTGTGTCA[C/T]ATTCTTCTTCACACT	54542
rs779088493	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122895660	AGAGATTTTGTGCTT[C/T]ACAAGGAGGACTTCA	54542
rs779099120	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122850552	GGTTCAAGCGATTCT[C/G]CTGCCTCAGCCTCCC	54542
rs779133221	snp	C/G	3.42936e-05	0.00414072	intron-variant	RC3H2	GRCh38.p7	9:122897259	TTGCACCAACCTATA[C/G]TAAAATCTTGAATGC	54542
rs779146972	snp	C/T	1.67959e-05	0.00289787	missense	RC3H2	GRCh38.p7	9:122897446	TGTGCACATTCTCAT[C/T]AAATTCATTATAGCA	54542
rs779150742	snp	A/G	3.31603e-05	0.00407174	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122880141	CTAACAAACAGAAAT[A/G]AGAATGCTTTTTACT	54542
rs779209301	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122903675	TCTGCTTTTTCTAAA[C/T]GTAACTAGAATATGT	54542
rs779229093	snp	C/T	1.65982e-05	0.00288077	missense	RC3H2	GRCh38.p7	9:122849712	GTTTTCAGAATGAGG[C/T]TGCCAGCACTGACAG	54542
rs779232264	snp	A/C			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849106	CTAACTCCACTCTTC[A/C]AAATTAAAAAAAGAA	54542
rs779238211	snp	C/T	1.65627e-05	0.00287769	missense	RC3H2	GRCh38.p7	9:122857964	GAGGAGAAGGTGGTG[C/T]TGGTGACTGTGTTGC	54542
rs779238710	snp	A/G	1.71846e-05	0.00293122	intron-variant, nc-transcript-variant	RC3H2, SNORD90	GRCh38.p7	9:122880245	CAGATTCCACAGTAG[A/G]AGTATCAGTGATGAA	54542
rs779244180	snp	A/T	2.057e-05	0.00320696	intron-variant	RC3H2	GRCh38.p7	9:122890297	TAAAAAAGGTAAGAT[A/T]GTAACCTATCTTACC	54542
rs779271761	in-del	-/AT			intron-variant	RC3H2	GRCh38.p7	9:122891590	CAGCATTCAACACAC[-/AT]GATTACTCATTACTC	54542
rs779283836	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122863869	AGCCTTCCCAGGTAG[C/G]TGGGATTACAGGCAT	54542
rs779320994	snp	A/G	1.66275e-05	0.00288331	intron-variant	RC3H2	GRCh38.p7	9:122860137	ACCAATTTTACTGGA[A/G]AGAAAATTTAACAAA	54542
rs779337519	in-del	-/A			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122881459	TGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	54542
rs779339934	snp	A/G	1.66021e-05	0.0028811	missense	RC3H2	GRCh38.p7	9:122851424	TTGCATCTTCTGTAT[A/G]ATCACTCTGTAACTA	54542
rs779361083	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122883691	AAAAAGTCATTTATA[A/G]AACACATAGCTGGGT	54542
rs779372553	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122904739	GCAGAAAGCTGAAAA[C/G]CTAGGAGAAGACTTG	54542
rs779374237	snp	C/T	3.43962e-05	0.00414691	intron-variant	RC3H2	GRCh38.p7	9:122857885	AGTCAGCTGTTTGAC[C/T]TATCCCTGCAACATT	54542
rs779393329	snp	C/G/T	4.99208e-05	0.00499583	intron-variant, missense	RC3H2	GRCh38.p7	9:122853897	GGTATAACCAAGATG[C/G/T]AGCAGCAGAAAACAA	54542
rs779484116	snp	G/T	1.67789e-05	0.00289641	missense	RC3H2	GRCh38.p7	9:122897442	GGTTTGTGCACATTC[G/T]CATCAAATTCATTAT	54542
rs779576172	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122884303	TCTCTAAAAAAAAAA[-/T]TTAAACACACAGAAC	54542
rs779595581	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122870032	CTCATTATTCTTTTC[C/T]TCAGAGTTCCTATAC	54542
rs779703065	snp	C/T	0.00688689	0.0582753	intron-variant	RC3H2	GRCh38.p7	9:122875315	TGTACAGTGCCCAAG[C/T]TAGCCACTGAGGAAA	54542
rs779705560	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122869186	CTGGGATTACGGGTG[-/T]TGAGCCACCATGCCT	54542
rs779774540	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122885725	ACATTCACAATGTGT[A/C]CAACCATCAACTTTG	54542
rs779798284	in-del	-/A	1.66056e-05	0.00288141	frameshift-variant	RC3H2	GRCh38.p7	9:122849742	GATGTGGTGATGGGG[-/A]GGCAACTTGCATTGC	54542
rs779847835	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882026	CCCAGGAGTTCAAGG[C/T]TGCAGTGAACTATGA	54542
rs779878047	snp	C/T			missense	RC3H2	GRCh38.p7	9:122865530	CAATTTTCCCTGTTG[C/T]TTCAGTACTTCCTAT	54542
rs779922325	snp	C/T	1.68727e-05	0.00290449	intron-variant	RC3H2	GRCh38.p7	9:122854510	GAATGGAGAATCATA[C/T]AGAATTAAGAAGAAC	54542
rs779943768	in-del	-/A/AA	0.10892	0.207262	intron-variant	RC3H2	GRCh38.p7	9:122893029	ATGATCTGGTACCTT[-/A/AA]AAAAAAAAAAAAAAA	54542
rs779971639	snp	C/T	8.32466e-05	0.00645108	intron-variant	RC3H2	GRCh38.p7	9:122854625	CATAATCTACAGACA[C/T]GTAGAATGAAACAAT	54542
rs779973451	in-del	-/C			intron-variant	RC3H2	GRCh38.p7	9:122867255	CAGCCCCCCGCCCGG[-/C]CAGCCGCCCCGTCCG	54542
rs779973813	snp	A/T	1.67668e-05	0.00289537	missense	RC3H2	GRCh38.p7	9:122849634	ACCTCCTTTCAGCTG[A/T]TAACCATCTTCCCAT	54542
rs779991026	snp	C/T	3.55499e-05	0.00421588	synonymous-codon	RC3H2	GRCh38.p7	9:122897480	TGGACAGGACAGAAA[C/T]TCTGTCCATTGAGCT	54542
rs779996985	snp	A/G	1.65605e-05	0.0028775	missense	RC3H2	GRCh38.p7	9:122858907	GGTACTGGAGGAACT[A/G]GTCCATACGGCTGCG	54542
rs780053440	snp	A/G	2.05785e-05	0.00320762	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880324	TTAGAAAACTTATAA[A/G]CTGTATTAACTCTCT	54542
rs780054882	snp	C/T	2.46333e-05	0.00350942	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880352	TCTGAGGTCAGAATA[C/T]AGATAAATTTGAGAC	54542
rs780057937	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122889848	TAAGATTAATAAAAA[C/T]GGATTTATATTGGCT	54542
rs780074792	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122857476	GCCCAGGATTCATAT[C/T]CCAGCTATTTACAGC	54542
rs780124932	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122860323	TGATCATCGTAACAG[A/T]TGTCATATTCCTGTG	54542
rs780167344	snp	A/G	6.64121e-05	0.00576209	missense	RC3H2	GRCh38.p7	9:122849739	ACAGATGTGGTGATG[A/G]GGAGGCAACTTGCAT	54542
rs780172859	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122866568	CGCCGCCACGCCTGA[C/T]TGGTTTTCTTATTTT	54542
rs780174550	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861897	GTTTAGAGTATAAAG[A/G]TATTTTAGGACTGTG	54542
rs780177251	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122879133	AGGCACGATGGCTCA[C/T]GCCTGTAATCCCAGC	54542
rs780220000	snp	A/T	1.90761e-05	0.00308832	intron-variant	RC3H2	GRCh38.p7	9:122849833	CCTCCCTGAGAAAAA[A/T]GAAATGACATTAAAA	54542
rs780240893	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905927	CTCCTCAAAAGCTGG[C/T]AAAAATAAAAAATTT	54542
rs780385373	snp	C/T	1.65608e-05	0.00287752	synonymous-codon	RC3H2	GRCh38.p7	9:122865405	ACCATTAGCGCCAAC[C/T]TTTCCCACTTTCTTC	54542
rs780385920	snp	C/T	1.6599e-05	0.00288084	synonymous-codon, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879800	ATTTTGTATGAAGTC[C/T]ACAAGGCCATGAACT	54542
rs780391420	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122900190	CATAATTAATACTGA[A/G]AAGTTTAATTTCTAC	54542
rs780393048	snp	C/T	3.3151e-05	0.00407117	synonymous-codon	RC3H2	GRCh38.p7	9:122890355	CCTGACAGCGGCCCA[C/T]AGATTGGCAGACAAC	54542
rs780406589	snp	C/G	1.65647e-05	0.00287786	missense	RC3H2	GRCh38.p7	9:122854035	AATTCCACTTCTGTT[C/G]CATGGCCAAAGCATT	54542
rs780411563	snp	A/T	3.40942e-05	0.00412867	intron-variant	RC3H2	GRCh38.p7	9:122890556	TACACCTTTAGGAAA[A/T]GGGAAACAAAGGGAG	54542
rs780412568	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122877365	GCTATGGTGCCCAGC[C/G]CTTAACTTGCATTTT	54542
rs780439853	in-del	-/AAACAAACAAAC			intron-variant	RC3H2	GRCh38.p7	9:122870382	TCTGTCTCCAAAAAC[-/AAACAAACAAAC]AAACAAACAAACAAA	54542
rs780446986	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122892228	GTGATTCTCCTACAC[C/T]GGTCTCCTCAGTAGC	54542
rs780537928	snp	C/T	1.65776e-05	0.00287898	intron-variant, missense	RC3H2	GRCh38.p7	9:122853914	GCAGCAGAAAACAAA[C/T]ACATTAAGCATGAAG	54542
rs780555331	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122850659	ATGTTGGCCAGGCTG[C/T]TCTTGAACTCCTTGT	54542
rs780610119	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122870230	AAATACAAAAATTAG[A/C]CAGAAGTGGTGGGAC	54542
rs780626157	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122886623	GAAGCCAGAAGTTCC[A/G]AAGTTACAGTGGGCT	54542
rs780632796	snp	A/G	1.65872e-05	0.00287981	synonymous-codon	RC3H2	GRCh38.p7	9:122858085	GGTCTTCAAATGACC[A/G]CAAGGTTCCTAATGG	54542
rs780651187	in-del	-/GAGACG			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907079	CATATTTTTTTTTTT[-/GAGACG]GAGTCTCACTCTGTC	54542
rs780708404	snp	C/T			missense	RC3H2	GRCh38.p7	9:122854234	CTGGAATGCTTTCTA[C/T]GACCAGATAAATCAG	54542
rs780725201	snp	C/T	1.65608e-05	0.00287752	missense	RC3H2	GRCh38.p7	9:122858919	ACTGGTCCATACGGC[C/T]GCGGAGGAGGAGGCT	54542
rs780746827	snp	C/T	1.65831e-05	0.00287945	missense	RC3H2	GRCh38.p7	9:122851412	GTTTAGTATCTGTTG[C/T]ATCTTCTGTATAATC	54542
rs780750830	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122885940	TCACCCAGGCTGGAG[A/T]GCAGTGGCACGATCT	54542
rs780751039	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122899542	TTAAAGTAACCAAAT[C/T]TTCCAAGTTATAATT	54542
rs780816538	snp	C/T	3.76265e-05	0.00433726	intron-variant	RC3H2	GRCh38.p7	9:122890193	CAAATTTATCTTTAA[C/T]TATATCAAGATTTGT	54542
rs780886916	snp	C/T	1.67214e-05	0.00289144	intron-variant	RC3H2	GRCh38.p7	9:122854637	ACATGTAGAATGAAA[C/T]AATGGTCAAAAAAGT	54542
rs780926238	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122871793	CTACAATGTAAGCCC[A/C]CGGAGGACAAGACTT	54542
rs780948925	in-del	-/CAAT	5.06907e-05	0.00503416	intron-variant	RC3H2	GRCh38.p7	9:122865670	TACCTGTTTCAAAAA[-/CAAT]CAACAGATTGGTGAA	54542
rs780955905	snp	A/G	1.65633e-05	0.00287774	synonymous-codon	RC3H2	GRCh38.p7	9:122877563	GCACATGCTAGTCTT[A/G]TATTTGCTGTTTGGC	54542
rs780959525	snp	A/C	2.10033e-05	0.00324056	utr-variant-5-prime	RC3H2	GRCh38.p7	9:122897515	GCACAGGCATTGTGG[A/C]AGCTGGATGCTCGGG	54542
rs781000635	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122878512	CCTGACCTTGTGATC[C/T]GCCCGCCTCAGCCTC	54542
rs781002019	in-del	-/A	1.68042e-05	0.00289859	intron-variant	RC3H2	GRCh38.p7	9:122854653	ATGGTCAAAAAAGTG[-/A]AAAAATCAGTGTACT	54542
rs781121064	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122858233	CCTAGTCTATTCTCC[A/G]TACACTTAAAATAAA	54542
rs781132453	snp	A/C/G	4.16964e-05	0.00456583	intron-variant	RC3H2	GRCh38.p7	9:122855169	ATCAGGCTAGGTATT[A/C/G]TCTAAATGGATTACC	54542
rs781140796	snp	A/T	6.74661e-05	0.00580763	intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880548	ATTCTAATACTCTTC[A/T]ATGTAACAGCAATGA	54542
rs781170762	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122876764	TAGTATTAAACCTTA[C/T]ATACATTAACTTTTA	54542
rs781192213	snp	A/C	5.40657e-05	0.00519903	intron-variant	RC3H2	GRCh38.p7	9:122849851	AATGACATTAAAAAC[A/C]AATTAGCTTTAAGTG	54542
rs781222514	snp	A/G	1.75197e-05	0.00295966	intron-variant	RC3H2	GRCh38.p7	9:122890571	AGGGAAACAAAGGGA[A/G]CTAAAGTTTTTTCAA	54542
rs781245178	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122903344	TAAGTAGTTACTAAA[A/C]CCTTGTTATGAAGTT	54542
rs781279302	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122859773	GTATTTAGAAGCACA[A/G]ATCCTTGGGGAAGGA	54542
rs781286929	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122862137	AAAGGCAACAAGATC[C/T]ATGATAAGGTCAACA	54542
rs781296683	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122878082	TACAATGAGGCAGAA[-/TT]TATTAAAATTTCACT	54542
rs781322127	snp	A/T	1.65611e-05	0.00287755	missense	RC3H2	GRCh38.p7	9:122865435	CACGGTCTCCAGAGC[A/T]CTTAAGGTACTGTCA	54542
rs781377048	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122882009	CAGGAGGATGGCCTA[C/T]GCCCAGGAGTTCAAG	54542
rs781520764	in-del	-/TAAC			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849220	TAGAAATAAATAAGT[-/TAAC]TAAGTCTACTTTCAC	54542
rs781521395	snp	A/C			intron-variant	RC3H2	GRCh38.p7	9:122903826	TCTTCAAAAATTGAA[A/C]GTGGAAGTAAACAAC	54542
rs781568315	snp	C/G	1.65971e-05	0.00288067	intron-variant	RC3H2	GRCh38.p7	9:122855427	GAAAATCAATAAAAG[C/G]ACTGTTGGCAATTAC	54542
rs781576568	snp	C/T			intron-variant, upstream-variant-2KB	RC3H2, SNORD90	GRCh38.p7	9:122880916	ACCACAGAAATAAGG[C/T]ACAAAGATAAGATAA	54542
rs781587985	snp	C/T	1.65872e-05	0.00287981	missense	RC3H2	GRCh38.p7	9:122892974	TTCTTTGCAACCTCA[C/T]AGTGTTTATTCTCAC	54542
rs781592377	snp	A/G	1.66186e-05	0.00288254	intron-variant, downstream-variant-500B	RC3H2, SNORD90	GRCh38.p7	9:122879911	TGGGGGTTGGGGGGG[A/G]AGAATGTTAGCAGTA	54542
rs781653701	snp	C/T			intron-variant	RC3H2	GRCh38.p7	9:122854342	AATAACCATATGTTT[C/T]ATGTGACAGATCAAC	54542
rs781661703	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122893184	AGTCAAACACCTAGC[C/G]AAACTGCTTTCCACA	54542
rs781675742	snp	C/T	1.65603e-05	0.00287747	missense	RC3H2	GRCh38.p7	9:122859982	TGAAAATACTGAATG[C/T]TTTCAGAATGCGGAG	54542
rs781727186	snp	C/T			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122907183	CTCCTGCCTTAGCCT[C/T]CCCAGTAGCTGGAAT	54542
rs781734933	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122901144	TGCTTCTTTAACTGT[C/G]ATATATGTATACATC	54542
rs796153887	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122868869	TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	54542
rs796178354	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122861439	AGGTTGTGGTGAGCC[A/G]AGATCACGCCATTGC	54542
rs796180439	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122865910	ATATGTATTTTTTTT[-/T]CCCCTCATGCCACTT	54542
rs796370157	snp	A/G			intron-variant	RC3H2	GRCh38.p7	9:122901983	TGCCCAGGCTGTAGT[A/G]CAATGGCGCGATCTC	54542
rs796450087	snp	A/G			downstream-variant-500B	RC3H2	GRCh38.p7	9:122849396	GTTGTCCAAATTCCA[A/G]TCATTTCTGGAAAGT	54542
rs796457463	in-del	-/TT			intron-variant	RC3H2	GRCh38.p7	9:122891013	ACCAAATCTGCCCCA[-/TT]TTTTTTTTTTTTTTT	54542
rs796516352	snp	A/T			intron-variant	RC3H2	GRCh38.p7	9:122897025	AGTGAGACTCTGTCT[A/T]AAAAAAAAAAAAAAA	54542
rs796650577	in-del	-/CCT			upstream-variant-2KB	RC3H2	GRCh38.p7	9:122905313	CTCCCTCCACCTCCG[-/CCT]CCTCCTCCTCCTCCT	54542
rs796822634	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122883895	GCTACTTTGGAGGCG[C/G]AAGTGGAGGATCACT	54542
rs796837095	in-del	-/T			intron-variant	RC3H2	GRCh38.p7	9:122891036	TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTCA	54542
rs796886559	in-del	-/AA			intron-variant	RC3H2	GRCh38.p7	9:122897049	AAAAAAAAAAAAAAA[-/AA]GGCCACATAAGATAC	54542
rs796895882	snp	C/G			intron-variant	RC3H2	GRCh38.p7	9:122852458	CGGGAGGTGAGGGGC[C/G]CCTCTGCCCGGCCGC	54542
rs797009221	multinucleotide-polymorphism	AC/GT			intron-variant	RC3H2	GRCh38.p7	9:122886227	TCCACATGCAGCATG[AC/GT]TCAGTATTTATTCCT	54542

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