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

RCBTB2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs527258132	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496853	GGAGAGGGGAGAGGA[G/T]GGGAGGGGAGACCCT	1102
rs527258651	snp	C/T	0.000399281	0.0141238	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504290	CTTTCACACGGGCAG[C/T]GGCTTCTCTCAGATA	1102
rs527301987	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503565	TTTTTTTAAGACAGA[A/G]GAGTCTTGCCTTGTC	1102
rs527338579	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48518283	TGTACCAGGGCTAAG[A/C]TCTCCTGATGCCAAA	1102
rs527396039	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48511387	TTCTGTTACACCTAT[A/T]TTTTTTATTAAAGTT	1102
rs527401143	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48516346	GGCAGCCGTAACAAA[A/G]TAGTGACAAACGAGG	1102
rs527477115	snp	C/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488934	ATTTTGCTGCTGTTT[C/T]GGGATTAAAAAAAAC	1102
rs527548627	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510145	ATTTTACTCTTCCTC[A/G]TAGTGACAGCTTGGG	1102
rs527576066	in-del	-/CT	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499301	ACTGACTCAGGCCCA[-/CT]CAGTCTGAAATAAGT	1102
rs527674797	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48512956	CATTATACGAAAATA[C/T]ATGTAGCACAGCTTC	1102
rs527711708	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48518318	GTCATGTTCCCTCAC[A/G]TGCCACTTGGATCAT	1102
rs527734668	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505054	TTTATTTCTTTCTTT[C/T]TTTTTTTTTTTCTTG	1102
rs527737510	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512256	ATGTACTTGTGGCAC[C/T]GAGTCTTTCCTCTCA	1102
rs527884886	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489778	GTGGTATCAGCCAGC[C/T]GAATAATGGAACATT	1102
rs527953012	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526463	ATCGCTTGAACCCAG[C/G]ATGTGGAGGCTGCGG	1102
rs528130858	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508155	AGTCAGGCTTTCCTG[C/T]AATGGGCCGCAGAAG	1102
rs528338137	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520830	AAATTACGTTAGGCA[C/T]ACCTAGCAAAAAAGA	1102
rs528479620	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496078	GTTACTTCATTTTTT[A/T]AAAAATATTAAATAT	1102
rs528504945	snp	C/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48530909	ATAAAAGACATTGTA[C/G]AGCACGATAAAGAAC	1102
rs528638685	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48502297	ACGGTTTAAGACCAG[C/G]CTGGGCAACACAGAG	1102
rs528784606	snp	G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48524137	TACATTATTTCAATG[G/T]GATGCATACATAATA	1102
rs528915401	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502357	AATTAGCCAGGCATG[C/G]TAATGGGTATGTATA	1102
rs528939840	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509267	GGGAAGTCAAGACTA[C/T]AGTGAGCCGTGATTG	1102
rs529148709	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530061	ATGCCTGGCTCATTT[C/T]TTTTTTGTTCGTTTT	1102
rs529149178	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514368	TCAGAATGGCACACA[A/G]TTTAAAACTTATGAA	1102
rs529357643	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524324	CCATGATGTGATAAA[A/G]TGTATTCTAAATAAC	1102
rs529368725	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48505476	AGAACCGTGCCAGAC[A/G]GGGAAAATGGTTAAC	1102
rs529403653	in-del	-/ACTTCTTCCTTCCTGTTTCGC	0.0130921	0.0798413	intron-variant	RCBTB2	GRCh38.p7	13:48492665	TCTGGTGTGGTTCGG[-/ACTTCTTCCTTCCTGTTTCGC]ACTTCTTCCTTCCTG	1102
rs529574325	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531681	CTTGTTGCTTTTACC[C/T]GCTGCTTAATAACAC	1102
rs529691599	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527101	TCTGCTTACAAATGT[A/C]CCCCCTTTTCTGCAT	1102
rs529696407	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492018	CATGTTCAAAATGGG[G/T]CCCTCTGTTCTGTCC	1102
rs529714370	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520040	TAAAGATACTCAACT[A/G]GTAAGTATAATGCAA	1102
rs529818415	snp	A/G	3.29478e-05	0.00405867	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499681	ATTCCAGGAAGGCCC[A/G]GTAAACAGGATATGA	1102
rs529819344	in-del	-/ATATATAT	0.409382	0.192607	intron-variant	RCBTB2	GRCh38.p7	13:48525374	AGCAAAGGATTCATG[-/ATATATAT]ATATATATATATATA	1102
rs529855029	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498785	CTCAAACTCCTTTGA[C/T]TTTCAAAGTCCAGAG	1102
rs529880026	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48525665	TCTAGAGCATACACA[C/G]AAATATTCCCAATAG	1102
rs530095750	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501615	CCCCGCTCCACTGTA[C/T]GCTTGTAAGAGCAAA	1102
rs530097385	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492984	TGATATTTCCCCCAA[A/T]ATGTTGCTCCTATCT	1102
rs530134656	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501321	TTTTTGGTCTGGAAA[A/G]GCCTTGATCTTCTCT	1102
rs530260124	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493900	CATTTGCAGTACCCC[A/G]GTGCGTAGGGCAGTG	1102
rs530372069	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507139	CCGTCCCGGGGCATG[A/G]CCTTGTGACATATAC	1102
rs530393161	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48494671	CAGATGCAAACACCA[C/T]GTGCCACCATCTTGA	1102
rs530469404	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48520128	CGGATAAGGGATACT[C/G]TACCTGTGTCAGTCT	1102
rs530571401	snp	C/T	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48529019	ACAAGAGTGATGAGT[C/T]AGATCTTCAGTACAA	1102
rs530602924	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492234	ACAGAGAGGCCTGTG[A/G]ATGCAATCTTCTCTG	1102
rs530710520	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489501	TTTAATTGCCAGGGC[C/G]TTTTGTCAATTCTAA	1102
rs530752856	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48500422	AATTAGCCAGGCATG[A/G]TGGTGTGCGCCTGTA	1102
rs530868520	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48522862	CTCATAATAGACAGA[C/T]AAAAACAATAATCAA	1102
rs530913035	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48494780	TCTGACCATGAAACA[C/T]TCTGTGTTGTAAGTG	1102
rs531010014	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501418	ATTCCCAGGCAGAAA[C/T]GGTAACTGATGGACG	1102
rs531041590	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514245	ATCTAATAACTGAGA[A/C]AGCTACTAAGTAACT	1102
rs531113519	in-del	-/ATTA			intron-variant	RCBTB2	GRCh38.p7	13:48527274	ACTATGTGTTACTTT[-/ATTA]GTTTTTCCCTTATAT	1102
rs531198088	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501677	GTGCCTAATATAGTT[C/G]GACACTTAGAATATA	1102
rs531316923	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489809	TGGGCCAGAATAGCA[C/T]ATACTGAGACCAGGG	1102
rs531352164	snp	C/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48497991	CCACATGCCCACTTC[C/T]AGACCACACTTTGGG	1102
rs531385430	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48516024	GAACTGAATGTTCAG[C/G]AGATACTTTAAATAT	1102
rs531405614	snp	C/T	1.65293e-05	0.00287479	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510771	CGTAGCCACAGGCGA[C/T]CTGGAAGGAAAAAAA	1102
rs531464337	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504368	TGTACAGACATCTCA[C/G]AAGTCAATTTTGTCC	1102
rs531588784	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488569	TGGGTGATAATGATG[C/T]GTCCAAGCAGGTTCA	1102
rs531608549	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48505870	AGAACCGAAAAAGGC[C/T]TCCTTCCGTGACTAA	1102
rs531633027	in-del	-/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533810	ACACTTAAATTGACC[-/T]TGAGTGGGTTTTGGT	1102
rs531673976	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48499876	CCCTGCTGTGGCTCC[C/T]CACTTTCTTTGCTGG	1102
rs531712814	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48505703	CGGATCAGAGTCAGA[A/G]TGTAGTTCTAGGGCC	1102
rs531770818	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512285	CAAAGTGCTTCACAT[A/T]CATAAATCCTCACAA	1102
rs531787942	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48506565	GGGGATGAGTCTAAG[A/T]AAACCCCCGGCTGGC	1102
rs531961074	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48523850	GTAAAATTAAACTCT[G/T]TAAAATTAGAATGGT	1102
rs532012417	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48490661	AAGTATGTCTGCCTA[C/T]AAAGAGTTGATGGAA	1102
rs532013310	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519237	CATCTGCAGGGCTTT[A/G]GCTATTCTCAGACTC	1102
rs532039608	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526938	AATAATAATAAATAG[A/G]TTTTTTTTAAATAGG	1102
rs532075768	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526970	GGATTAAATAACATA[C/T]CCAATGAGTAGCATT	1102
rs532120164	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48491476	CACAGCATACTATAC[A/G]TAAAAATGTGCTTCA	1102
rs532156857	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499486	AGTAACAAGGGAAAC[A/G]TGTTTGGATTCAACA	1102
rs532249975	snp	C/T			missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496270	TTGATAGTTTGTTGG[C/T]AGAGCTTTTTCAAAC	1102
rs532312211	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498059	GAGGCCACATGTGTG[G/T]GTATTTCCTCCCTTA	1102
rs532343015	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498706	TTGCACTCCAGCCTG[C/G]GCAACAAGAGTGAAA	1102
rs532538490	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48492404	CATTAGACAAGCTTC[C/T]ATTTCCCACATCTTA	1102
rs532680134	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48501197	TTCACAGGCGTAGAC[A/G]TGTGTCAGCACTCAT	1102
rs532746217	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512362	TGATTTTATACAATT[A/G]GGTTATTGGTGTTAT	1102
rs532755741	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48523197	TACATATTATCTATG[A/G]CATCTTAGCAGATCT	1102
rs532848214	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503516	CTGCTCTAAGTTCAC[A/G]ATTGATGAGGAGGTA	1102
rs532992646	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48509354	AAAAAATAACAGGCC[A/G]TACAAATCCATCGTT	1102
rs533164964	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517580	GTAAAGGGAAGCTAG[C/G]ATGCACGGAGCAGCT	1102
rs533202774	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525543	ACCCTACTCTATCCT[A/G]TTTTATCTTGTTCAA	1102
rs533214814	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508863	TTCTCCCACCTTGAC[A/G]CCCCACAATCCATCT	1102
rs533419166	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518238	CTTGTCCCTGCTATC[A/G]GCATCACCCTGTGAG	1102
rs533487259	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528251	TTAATCAGGGGCTTC[C/T]AAATGCTAATAATTC	1102
rs533820080	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48511611	TTTCTGAACAGCTGC[-/A]ATTTAATTCAAGGAA	1102
rs533831016	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48505050	TTTTTTATTTCTTTC[-/T]TTTTTTTTTTTTTTT	1102
rs533842677	in-del	-/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48494865	GTTTTGAGGTAGTAC[-/T]TTTTTTTTAATGTTA	1102
rs533899325	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531754	TAGAATACTCATTCT[C/G]TGAGCCTAAGTGGCT	1102
rs533965315	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503779	GTCTTGAACTCCAGA[A/G]CTCAAATGATCCGCC	1102
rs534007144	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508986	GGCAGATTCTGTGAG[A/G]CCAGGGATGGATGTG	1102
rs534049458	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48495541	GTAAACACCTTTGAA[A/G]CTAAGTCTTTGTGCA	1102
rs534199672	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510507	TCTAAAGGAATAAAT[A/G]CTCTTGTTAAATAAT	1102
rs534226066	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510951	GAATTGCAGTAAGAT[A/T]GCCATGAGTACCCTG	1102
rs534235638	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517018	AACCTTACCGGGAAT[A/G]TGGTCTGGTGTATAA	1102
rs534311822	snp	C/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48507287	TGTGACCCAAGCAAC[C/G]GCTAAGGAATCCTGC	1102
rs534346492	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506837	AGGCAAAGACTTCTA[C/T]ATTTTTTGGAATCAT	1102
rs534347883	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513857	TGCATAGCAAGCCCC[A/C]CTTATCTGCAGGAGA	1102
rs534370603	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501479	GGACACACTTGGAGC[A/G]TGCGCTGGCTGCTCC	1102
rs534606911	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512633	ATTTGAGGGAGGTGG[C/T]TATTTTAATCAAATG	1102
rs534794062	snp	C/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488839	TCCTATGAGACTTTA[C/T]CCGAGTAACTGCTTG	1102
rs534873862	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48490683	TTGATGGAAGAAAAA[C/G]GTAAGCCATAAAAAG	1102
rs534917850	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520310	TGACCCAATCAACTC[C/T]GTGCCCAACTGTCAA	1102
rs534919986	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525341	TAAGAATAAAACAAA[C/T]GACACAATTCAAAAG	1102
rs534958565	in-del	-/A	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48529253	TTAATCCAATTTTTC[-/A]AAAAAAAATCTTAAC	1102
rs534992881	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521119	ATTTTTCTGTTAACA[C/T]TTTTGTAGGACTCTC	1102
rs535077650	snp	A/G	1.74193e-05	0.00295116	intron-variant	RCBTB2	GRCh38.p7	13:48501919	ACAGACATAATGAAC[A/G]CACAGGACAGGATAT	1102
rs535077994	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493525	GACTCTGCAGGCCCT[C/G]CCTCCTCCCACACAC	1102
rs535122023	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514658	ATTCAAGGGTTGAGA[C/T]TTCTTGGACCGTTCA	1102
rs535137311	snp	A/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48508224	TATGACATATACTTG[A/T]CTTTCCCATCCCTGG	1102
rs535203302	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534423	CCTTACTTTACAGAT[A/G]AGGCAACTCAGGCCC	1102
rs535334381	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513367	AAAGCACACACCCAT[A/G]TACTACTACTTAAGT	1102
rs535502231	snp	A/G	6.59685e-05	0.00574281	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515294	AGTCTCCGAGGTTCA[A/G]TGGTGCTCTGGACGT	1102
rs535527248	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48528517	AAATAATATCGATAT[A/C]TTTTAGGGTACCAGC	1102
rs535552503	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48509644	AAGTTTTATTTAACC[A/T]ATAAAATTAACCTAT	1102
rs535686828	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48508556	TTACAGGCATGTGCC[A/C]CTGTGCCCAGCTAAT	1102
rs535709611	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507460	CACACTTTTATTTTG[G/T]AGCCAATCTTAATGG	1102
rs535794357	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48530968	AAAACCCAGTTCCCC[A/C]TGTTAAACATCACCT	1102
rs535896121	in-del	-/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48499928	CTATTCAGCAAGGCT[-/G]TATATACAAACCTGC	1102
rs535917691	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518783	AGGCCACAATAGAGC[C/T]AAGGATGGAATTTTG	1102
rs535957052	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509097	GCACTTTGGGAGACC[C/G]AGATAAGAGGATCAC	1102
rs535976074	snp	C/T	9.91424e-05	0.00703998	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512019	TAACTTCCTTACCTC[C/T]CCCGTGTCTACTACT	1102
rs536001669	snp	A/G	0.00187371	0.0305507	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533042	CCTCCTCGCAGGCCG[A/G]AGCCTTGTCCGCTCC	1102
rs536075595	snp	A/G	3.29582e-05	0.00405931	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490070	ATCTCTGGCTTTTGC[A/G]GGGGAAATGGAAAGG	1102
rs536125976	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48526642	AAAATAGCCTGGGCG[C/T]GGTGGCTCATGCCTG	1102
rs536283742	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516749	CATACATTAAGATCA[C/T]GAGCACCCACACTCC	1102
rs536323361	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505524	TCAGCATCATTCTTT[C/T]CAACAAATAAAGAAA	1102
rs536380868	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48494446	GCATCTCTATAGGCA[A/G]AACTGAACATCCATG	1102
rs536501489	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491754	TAATTAATGGGAGAA[A/T]GAAAGGACCCTAAAA	1102
rs536726812	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48520431	TATGGTGTCCCTAGA[A/G]TTCAGTCCTGGTTTG	1102
rs536756594	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48506216	CAGCATCGTACAAGA[A/C]CTGACAGGGACGGAG	1102
rs536759226	snp	A/T	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48513099	AGCAACAAGGTGAAA[A/T]TTAAATGCATGCAGT	1102
rs536877682	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48526253	AAATAAAATTGAATC[A/G]ATACCCTAGGAAGGC	1102
rs536884505	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506164	CAATGCAGGACCAAC[A/G]TGCAGGCAGAGCTGG	1102
rs536913946	snp	A/C	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48519534	TAACTCTACTGGCTA[A/C]TGGGATTCCAATGCG	1102
rs536952947	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48518899	GTTTTTAATTTTTTT[C/T]CTATTTTAAGTCTGT	1102
rs537121314	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48506805	CTTCAGATTTTAGCA[A/C]TTTGCAGTGACCTAC	1102
rs537153429	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48491121	TCCTCTCCAAGCTAC[C/T]GTAGGTAATTTATAA	1102
rs537223694	snp	A/C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496678	GCACACACACATGCT[A/C/G]TAAGAGTGCCCGCCG	1102
rs537357311	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48500928	TGAGACTAAAATGCT[A/G]TGTTGAGTGTGTGAC	1102
rs537400158	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532459	AGATTTATGGGACGG[A/G]AGCCTAGGGGTCGAG	1102
rs537494253	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529285	CGCCTGCTACAGAGA[C/T]CCTAATTGTTAAAGA	1102
rs537548871	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48511065	TGTATTTTTTAAATA[A/G]TTATTTTCTTTTTTG	1102
rs537846460	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490106	AAACTTTCCTGCAGA[C/T]GGGATCAATTTTTAA	1102
rs537848498	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498828	TCTCTATCTTCCTCA[C/T]CTCAGTGCCATTAAG	1102
rs537883236	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498135	TGGGTTGGGGGTGGA[C/T]AGAGCTTGGAATGCA	1102
rs537895695	snp	A/G			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503054	AAAACAAAACAAAAC[A/G]AACCACCACATGACT	1102
rs537921084	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525878	TAACATTTTAAAACA[C/T]GCAGAAGACAGTACT	1102
rs537932783	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533796	TTCTTCCACTGCACT[A/G]CACTTAAATTGACCT	1102
rs537958404	snp	C/G/T	1.66123e-05	0.00288199	intron-variant	RCBTB2	GRCh38.p7	13:48515372	TATGGGAAAAACCAC[C/G/T]GTTAGTTCAAGCAGT	1102
rs537959608	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48524734	ATCCTTGTAAAGTTG[C/T]CTTCTAGAGCAAAGT	1102
rs538086963	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48501102	CAGTGACAGAAGGAG[C/T]TGCGGTCACCCAGGG	1102
rs538096242	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497029	CCACCACTACTGCAG[C/T]CACACCCTTGGTGGT	1102
rs538124320	snp	A/C	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48531882	GGAGTCACGAAACTG[A/C]CTTAACTAAGACCCA	1102
rs538142166	snp	G/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48505903	GTGTTTACCAGCTGC[G/T]GCAGAACTGTGGGCC	1102
rs538164473	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510978	CCTGGCGTGAGCACC[C/T]GCCCCAGTTCACTAG	1102
rs538177479	snp	A/C	0.221737	0.248397	intron-variant	RCBTB2	GRCh38.p7	13:48532571	CGGGACCTGTGACGC[A/C]CCCCCAGCCACACCA	1102
rs538200400	in-del	-/GA	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48517945	TCCTTAAAAGAAGAC[-/GA]GAGGGCACACAGTGA	1102
rs538353764	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529972	CATGACTCACTGCAG[A/C]CTCAACCTTCCCGGC	1102
rs538365457	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534847	AGACTCTGAGAGAGT[A/G]TAGGTTAGTATTTCA	1102
rs538561535	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532469	GACGGGAGCCTAGGG[C/G]TCGAGGCCACAGAAA	1102
rs538588342	snp	A/C	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502322	ACAGAGAGACCCCAC[A/C]TCCAAAGAAAGTTTC	1102
rs538670033	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48490387	ATGATGGCATGGTAA[C/T]ACCTAAAGAATAGTC	1102
rs538902272	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524929	TGCTCTATTATAAAA[A/T]TACTAAAGTTATAAA	1102
rs538914486	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48499099	AGTTGCCTCTCTCCC[A/G]ACCCCCACCCCAACA	1102
rs538950166	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518802	GATGGAATTTTGTTA[C/T]GTTAGCTTTTAGTTA	1102
rs538984562	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533868	GCTATTCCTGTGAAG[C/T]AAGCTACTTGCTTTT	1102
rs539036493	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48499978	AGCAGCCCCAATGGC[C/T]GTGCTAATGGGGACA	1102
rs539069106	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489037	CTAATTCCAAAAGGG[C/T]TTCCTTTACATTACA	1102
rs539077670	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502436	GGCTGAAGGGTACAG[C/T]GAGTTATGATTGCAC	1102
rs539149787	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534666	AAAGAATGTGTTTCA[C/G]TAAAGATTTTAATTT	1102
rs539160435	in-del	-/ATTC	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48520969	TATTCATTATATCAT[-/ATTC]ATTCATTATAACACT	1102
rs539267021	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504636	ACCAGTTTCTGGCAG[G/T]CCTAATCACTGGCTT	1102
rs539440215	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510328	GAAAAGGAGGAGGGC[A/G]AAAGGGTGATTTGTA	1102
rs539498590	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531194	TTGTTCATTGATGCA[A/T]CCCAAGCATCAAGGA	1102
rs539499160	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503747	AGAGACAAGGTTTTG[C/T]CATGTTGCCCAGGTT	1102
rs539672426	snp	C/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48502031	GACAGATTTGCATCT[C/T]TGTAATCATTAAGAA	1102
rs539686669	snp	G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48531705	ATAACACGCATGTAC[G/T]GTCTAGCAGGAAATA	1102
rs539826340	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48525238	GGAAAAATATGCCAC[A/T]GAATGGGGGAAGATA	1102
rs539887101	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48522220	TAGTCTCAAAATTCA[C/T]ATGGGTCCTTAACTC	1102
rs539939262	snp	A/T	1.6492e-05	0.00287154	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515652	ACAAGCCTGACGAAT[A/T]AACTGTAGTTCTTCT	1102
rs540091027	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48499829	CCTCTGTGAGGACCA[C/T]GTTCTTCTCTCGAAG	1102
rs540195094	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531375	TGATCATACCCTTAC[A/G]AATATATAATATCAG	1102
rs540262083	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48496501	CTACCCAGGATGGCA[A/G]CCAAGCTGAGCAAAC	1102
rs540351859	snp	C/T	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48513952	ATAAAGTTTAATTTG[C/T]AAGTTAGGCATAGTA	1102
rs540362005	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48532126	TCGAACTGTTGCAAC[A/G]TTTTATGTAATTTTT	1102
rs540418363	in-del	-/TATATG	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48511412	AAGTTATCCTCTTTT[-/TATATG]TATATGTATATGTAT	1102
rs540453116	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493821	ATATCCTATTCATTT[A/G]TTGATCACCTATCTC	1102
rs540497314	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503167	AAGATCTGTTTGTAC[C/T]ACTTCTAGCCAGTAG	1102
rs540515019	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509163	AAAACCCTGGCCCTG[A/C]AAAAAACACAAAAAT	1102
rs540678959	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489307	TTGTCATTTTCATTT[A/G]CAGAGGCAAGTCCCT	1102
rs540803805	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48505335	TTAAGTGACAAAGCA[A/T]CTTTTAGGTGGAGAC	1102
rs540833580	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48523044	AATAGCAAAGTATTA[C/T]TTTCTAACATTTGGA	1102
rs540866975	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512250	ACTGACATGTACTTG[C/T]GGCACCGAGTCTTTC	1102
rs540890364	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496128	TTTTAGTTTAAGGTA[C/T]GAGGCAGACACCTGG	1102
rs540893508	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506263	GAGGGCAATGAGGCT[C/T]GCCAGGAACAGTGGC	1102
rs540929378	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509921	TACAATGACTGCAAC[A/C]CTGGTTTAAAAGAAA	1102
rs540930317	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505710	GAGTCAGAGTGTAGT[A/T]CTAGGGCCACGTTAT	1102
rs540935615	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499508	GATTCAACACACACA[A/C]AAAGAAATACTTCTG	1102
rs540938842	snp	A/G	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48508164	TTCCTGCAATGGGCC[A/G]CAGAAGAGTCAGAAG	1102
rs540999702	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48515518	ATTCCTTAGTTCCCC[C/T]AAGATCTTCAATTTG	1102
rs541015020	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491948	AACAAGGCCCCCATT[A/G]TTTTTCAGTTAAAGA	1102
rs541054947	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48513008	CAGGTGCAAAAAGCT[A/G]ATCAACTTCCCCATT	1102
rs541137455	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48490310	AATTCAATGCAACAT[A/G]GCATGAAAATCGCTA	1102
rs541189906	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48528731	CACTTGCAAAAAGGG[A/T]TAGTGTTAGCTGTAA	1102
rs541192437	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48491561	TTTTTAGAAATGACA[-/T]TTTTTGCCTACAGCA	1102
rs541226079	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48519994	CAAAGGAAATGTTCA[C/T]TAGAGCATTTCAGAT	1102
rs541253816	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520601	TAGTGAAATTTTAAT[A/G]TTAGCTCAAGGAAAA	1102
rs541451294	snp	G/T			missense, nc-transcript-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499636	CTACTGCCTCCTCAG[G/T]AGAAAGGCTGATGCT	1102
rs541457675	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48492671	TGTGGTTCGGACTTC[C/T]TCCTTCCTGTTTCGC	1102
rs541483584	snp	A/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48507118	GGGAAGGCCATGTGA[A/T]GCTGCCCGTCCCGGG	1102
rs541491306	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530195	GTGAGCCACCGCGCC[C/T]GGCCTGATTTGTAGT	1102
rs541508278	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501582	ACCTGTGTTATTTCT[C/T]GTTTCATGTATATTT	1102
rs541519153	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520734	TGAAGAATCGAGTGT[A/G]TAACCAAACTTCACT	1102
rs541554644	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529776	CCTTTGAAGTAAAAT[A/C]TCCAAGTAGAACTCT	1102
rs541558015	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48528820	ACATGGCTAATTAAA[A/G]TGGAACAATTATAAA	1102
rs541693867	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48492127	CCCTCTCATCCTCAT[C/T]CTCAGCTGACATGAC	1102
rs541695518	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48501063	TCCCATCTAAATACA[C/T]TCTAGAAAATGCTAA	1102
rs541696347	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513660	AATCATATTGTTCAT[C/T]TGGATCTTTTCAAAT	1102
rs541770746	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506924	GCATCCTTCACTGAT[C/G]TGCCCAACATCAGAA	1102
rs541907651	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508523	ATTCTCGTGCCTCAG[C/T]CTCCCAAGTAACTGG	1102
rs541977944	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521276	ATGCTGGCTTTGCAT[A/G]ATTATTTACAGTTTT	1102
rs542100608	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514723	ACAACCTTTTGGGGA[G/T]AAGTTTTATTTATTT	1102
rs542290885	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501642	CAAAAACAGCCTTAC[A/C]ATTTTTCTTGATTAC	1102
rs542371372	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525215	AAGAGCAGTAAACTT[A/G]AACAAAAGGAAAAAT	1102
rs542494452	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507899	GATTGGATGACTGGA[A/T]TAGGAGAAGACAATC	1102
rs542502695	in-del	-/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48526939	ATAATAATAAATAGA[-/T]TTTTTTTAAATAGGA	1102
rs542531078	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514228	TGAAACCAAGAGAGT[A/C]AATCTAATAACTGAG	1102
rs542775363	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512257	TGTACTTGTGGCACC[C/G]AGTCTTTCCTCTCAA	1102
rs543002782	snp	A/T	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48527381	TATGATATATATATA[A/T]GATATATATTTATAT	1102
rs543022721	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520728	GCAATATGAAGAATC[A/G]AGTGTATAACCAAAC	1102
rs543078099	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498590	ACAAAATTAGCCAGG[C/T]GTGGTGGTGCATGCC	1102
rs543089676	snp	C/T	4.962e-05	0.00498072	intron-variant	RCBTB2	GRCh38.p7	13:48512713	AATCAATGAGCTTTA[C/T]GCTGACTGTTCTCAC	1102
rs543163126	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519734	TAAGTACAACAGAGA[C/T]GTGAATACATTGCTT	1102
rs543170265	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48511903	ATGAGACCCTCAATC[C/T]TCTCAAGAGACAAAT	1102
rs543218906	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48498609	GTGGTGCATGCCTGT[A/G]ATCCCAGCTACTCGA	1102
rs543275575	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499163	TCTCTCTCTCTCTCT[C/G]TCTCTCACACACACA	1102
rs543278946	snp	C/G	1.64817e-05	0.00287064	stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512128	GGCTGATTAACTGTT[C/G]ATCCAGATCCTACCT	1102
rs543317040	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504917	ATGTGCGGTAATCTC[A/G]CTGACTTATTATGAG	1102
rs543338427	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533986	CACAGTGACCGTGTC[A/G]GTCTGTTTCGTCTGG	1102
rs543551911	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506604	GGGAGGCAGAAGCCG[C/T]GCTGGTCAGGTGGCA	1102
rs543604727	snp	G/T	0.00874735	0.0655527	intron-variant	RCBTB2	GRCh38.p7	13:48526939	ATAATAATAAATAGA[G/T]TTTTTTTAAATAGGA	1102
rs543862661	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506954	AAAGCCAAATAATGC[A/G]GTTCTTATGTTCCCT	1102
rs544066643	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491831	TCTTCCCCTAAATAC[G/T]AAATTAAGGACAGGA	1102
rs544109186	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519830	AGGGCAACTATTACA[C/T]AGGGAACTGATGACT	1102
rs544186168	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524134	TTTTACATTATTTCA[A/G]TGTGATGCATACATA	1102
rs544233984	snp	A/C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532712	GCGGCCTGGGCAGGA[A/C/T]GTAGTCGCGAGCAGC	1102
rs544237229	snp	G/T	0.00716266	0.059414	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489591	AATAATTACAGGCTG[G/T]TTTAAGTTTATTTTG	1102
rs544265967	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515818	CAGTTCTGTAGAAGA[A/G]GGCGAACACTGGTTT	1102
rs544280857	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517542	ACAGTATTAACTTGT[A/T]TCCAAAGTAAAGTTT	1102
rs544298130	snp	C/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48509308	CCCCAACCTGGAAGA[C/G]AGGGAGACTGTGTCT	1102
rs544349560	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530736	ATAGATGTCTGGCTA[C/G]CTCTTCCTTGTAAAA	1102
rs544454522	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48495662	CCAAATTGTTCTCCA[C/T]ACCAATTTGTACTCT	1102
rs544477759	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488949	TGGGATTAAAAAAAA[A/C]CCCAACACATTTGTT	1102
rs544514626	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496631	CTTCCCCTGCAATCT[C/T]AATGTCAGCTTCTCC	1102
rs544709846	snp	C/T	0.000388954	0.0139401	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533094	GCACGGTCAGGGGCC[C/T]GGCGCCGCGATGAGT	1102
rs544755987	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532038	CAACCACTTTTATTC[A/G]GCTCTGACAAGGTAA	1102
rs544899926	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503845	TGAGACACTGCACCC[A/G]GCCTCAGAACACTTC	1102
rs544952247	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516556	CCCTGCATATCTCTG[A/C]ATCTAAATTTCCCCT	1102
rs545035633	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526429	TAGTCCCAGCTACTT[A/G]GGAGGCTAAGATAGG	1102
rs545064262	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510037	AAGGCTTTCAAAAAT[A/G]TCAGAATAACGTGGA	1102
rs545082857	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48511594	TGCCCTGGAAGAGAA[A/G]TTTTCTGAACAGCTG	1102
rs545091998	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48504183	CCTGTAACAGCCTCC[C/T]AGGTCTCCCTTGCCT	1102
rs545107083	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497377	TTTCAAGTAATTCAA[C/T]GTAGACTGGGTGAGG	1102
rs545178348	snp	C/T			missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512794	CAATGACTTGTTTGT[C/T]TGACAGATTAGTAGA	1102
rs545194499	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518299	TCTCCTGATGCCAAA[G/T]CTAGTCATGTTCCCT	1102
rs545266097	in-del	-/AC	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48530586	TTAAGCTCCTCTCCT[-/AC]ACAGTTTCAAATACA	1102
rs545303007	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497865	TTCATTGTTTTTGGC[C/T]CCAAGCTTCAGACAC	1102
rs545367832	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48526572	TAATGAGCTATGATC[A/G]CACCACTGCACATTA	1102
rs545497558	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526807	TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	1102
rs545506617	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498763	CACTTGGGTATCTAA[C/T]GGGAAGCTCAAACTC	1102
rs545628504	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48515123	TTTCACAGGAAGAGC[A/T]AGCAACTCTCAACCA	1102
rs545636810	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490286	TGGTTTAATAAATTC[A/G]TATTTACTAATTCAA	1102
rs545715679	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533258	GCCCACCGCCGCCCC[C/T]CCCCTTTCTCGCAGA	1102
rs545752486	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532782	CCGCCTCTGCCTGCG[C/G]CCTGGGCTGGGTGTA	1102
rs545903028	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502664	TCATTATCAAAGTAA[A/G]GCCCTGAGCTCTTTC	1102
rs546208355	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494847	GTGCTGTTAAATGTC[A/G]TTGTTTTGAGGTAGT	1102
rs546224066	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48519955	ACTTTTTGAGCACCA[A/G]TTATGATGTTCAAAG	1102
rs546339395	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506241	ACGGAGGCCAACGCC[A/G]GGATCGGAGGGCAAT	1102
rs546406685	in-del	-/A			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534296	CAGGTTTGCTCTCAG[-/A]AAAAAGCTCACTTCA	1102
rs546480093	in-del	-/C			intron-variant	RCBTB2	GRCh38.p7	13:48509755	GCAGTTGAAAAATGA[-/C]AATTTGGTTCTTCAT	1102
rs546561827	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522816	AACATCAGAACATTT[C/T]ATCTGGTATTTTCTA	1102
rs546577203	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521652	GGCCTTTGCGCCTCA[A/T]CTGTCACTGTCACCA	1102
rs546689360	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497012	CAAGCAGAACCCCAT[C/T]CCCACCACTACTGCA	1102
rs546728035	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526913	AGAGTGAGACTCCAT[C/T]TCAAAAAATAATAAT	1102
rs546752511	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528586	CCACATAAATTTCAA[C/T]AGGATAATGATGGTT	1102
rs546825813	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48528368	ACTTAATGAGATCAA[C/T]TCTAAAGCTATGCTT	1102
rs546962093	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534198	AACAGGAAGTTGCAG[C/T]GATAGTGCAGAGAGG	1102
rs546962144	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526606	TAAGCAACAGAGCAA[A/G]ACTCTGTCTCTAAGA	1102
rs546986218	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48495149	AGGAAACTGACTCGA[A/G]GATGTTACAGCCTGT	1102
rs547015352	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48507176	CACCCGGCTCCACAT[-/G]GGAAGTCAGGGGTGG	1102
rs547105781	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48500184	GACCTTACTAGGAAA[C/G]AGAGCCTTTAAAGAG	1102
rs547230798	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504995	AAGGCTACGATGGCC[A/C]ACAGTGGAGAGCTCA	1102
rs547250677	snp	A/G			synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502752	GCGCCACGTGACGGC[A/G]GGCGTGGCAAAGCAG	1102
rs547469078	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48519337	GACTGACGGCTATTT[C/T]ATTTTTCCCTTGCAA	1102
rs547544590	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492922	AGACATTTCCATTTG[C/G]ATGTCTAATAGACAT	1102
rs547563806	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508646	TGACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTC	1102
rs547738543	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527855	ACACTCTTTTGATAA[C/T]GTGATAAACACATTC	1102
rs547897778	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520045	ATACTCAACTGGTAA[A/G]TATAATGCAAATATT	1102
rs548031898	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48499840	ACCACGTTCTTCTCT[C/T]GAAGGTGCACGCTGG	1102
rs548091012	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500136	TCTAAAAATTCCTGT[A/G]TTGAAGTCCTAATGG	1102
rs548093027	snp	G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48506662	GAGCAATTAATAAAA[G/T]GAAAAAGGGCCTTCT	1102
rs548129414	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506047	GTAAGGAAAAATACC[C/T]GGGGGCTCCTCAGGG	1102
rs548197482	in-del	-/A	0.236144	0.249616	intron-variant	RCBTB2	GRCh38.p7	13:48498730	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAATT	1102
rs548246552	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512994	GAAATCTAAAAATTC[A/C]GGTGCAAAAAGCTAA	1102
rs548331509	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48492938	ATGTCTAATAGACAT[C/T]ACATACTTCTCATAT	1102
rs548384290	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530068	GCTCATTTTTTTTTT[C/G]TTCGTTTTTCTGTAG	1102
rs548442781	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528808	AGTAAAATACCTACA[C/T]GGCTAATTAAAATGG	1102
rs548452310	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513763	ATTGGTGTCTGATAA[C/T]TTTAATGCCTGATAT	1102
rs548493250	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534453	CCAAGAGATTAAGTT[G/T]CTTTCATCAGCAACC	1102
rs548650681	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493018	ATATCTCAATAGATG[C/T]CACTTTCATCCTTAC	1102
rs548713145	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48493906	CAGTACCCCAGTGCG[C/T]AGGGCAGTGCCAGGC	1102
rs548778636	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48523978	TCAAATTGAATGAAA[C/T]GTAAGATTAACATAA	1102
rs548781479	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48521312	ATTTTGACCTGATTT[G/T]ATTAAATAATAGTGA	1102
rs548803864	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506766	ACAATGTGAAGATAA[A/G]CATTTATGAACTGCT	1102
rs548815124	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48490950	AATAATTCTCTTGAT[C/T]AGAACTATAACTTGA	1102
rs548922544	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48510285	CGACCTTGAATGTTA[C/T]TGACACCCCCTTAAG	1102
rs549050534	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498794	CTTTGACTTTCAAAG[C/T]CCAGAGCAAGCCTGT	1102
rs549119104	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516771	CCACACTCCTATAAG[A/T]GGAAGTTATAAATTT	1102
rs549122765	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48531472	GAGGTAGTCACCTCT[C/G]TGAAATGATGGCAAT	1102
rs549129813	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532409	TACTGCCACTGAGTT[A/G]GTGAGCCGGGCCGGT	1102
rs549285136	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503588	GCCTTGTCACCCAGG[A/C]TAGAGTGCAGTGGCA	1102
rs549317362	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48511710	TATGTTTTTAATACA[C/T]TGATATCTTTGCCAG	1102
rs549322111	snp	G/T	1.66452e-05	0.00288484	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502888	GCAGACGTGTGTGTG[G/T]AGTGACAGGCTGCAA	1102
rs549408649	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510969	CATGAGTACCCTGGC[A/G]TGAGCACCTGCCCCA	1102
rs549444923	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517700	TTTCTGAATAATCTT[C/G]ATGGCACTATTGAAT	1102
rs549618902	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491829	GATCTTCCCCTAAAT[A/G]CTAAATTAAGGACAG	1102
rs549639055	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525901	ACAGTACTATTTTAA[C/T]GTGTTATGGATACCA	1102
rs549721757	snp	G/T	3.2962e-05	0.00405954	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490062	AGTGATTCATCTCTG[G/T]CTTTTGCAGGGGAAA	1102
rs549748245	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503673	CCTACCTCAGCCTCT[A/G]TAGTAGCTGGGACTA	1102
rs549781337	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518640	CCCAATTTTATTATA[C/T]ATATAATTTTAGGAA	1102
rs549827380	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491696	AGTTAGGTGGCTGGG[C/T]AGTTTGATGCCTCAC	1102
rs549830602	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489835	CAGGGTACCAAAGGT[A/G]TCCAATTTAAGTGAC	1102
rs550101712	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497124	TTTACACAGAATTTG[A/T]TATGGTTGATAATGC	1102
rs550188153	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505189	ACCTAGGAGCCTTGG[A/T]TTCATCACATTGCAA	1102
rs550254253	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48499928	CTATTCAGCAAGGCT[A/G]TATATACAAACCTGC	1102
rs550317412	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48532015	ATCCAGAGCACTGTT[C/T]GTGAACTCAACCACT	1102
rs550344850	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48508825	CTTCCATTCCCATTA[C/T]CTGCTTCTCTGCTAC	1102
rs550348440	snp	A/T	0.0142736	0.0832652	intron-variant	RCBTB2	GRCh38.p7	13:48518476	AAAAAAAAAAAAATA[A/T]ATATATATATATATA	1102
rs550470314	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512294	TCACATTCATAAATC[C/T]TCACAACACAGGCAG	1102
rs550516307	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48516196	TGACACCAAGGAAAT[A/G]GTCCGAAGTTTTAGT	1102
rs550678672	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516794	ATAAATTTGTTTGAA[A/G]GAGTTTTACCTATTT	1102
rs550827985	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508238	GACTTTCCCATCCCT[A/G]GAAAGGGTGGAGAAG	1102
rs550833589	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48492220	TCTCCTTGCCTATTA[C/G]AGAGAGGCCTGTGGA	1102
rs550865347	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48499899	TTTGCTGGCCAGGGT[G/T]TTCAAACAATCATCT	1102
rs550870390	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524308	ATACAGAAAGCCATA[A/T]CCATGATGTGATAAA	1102
rs550874128	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48515024	ACATCTAAAATGCCA[A/G]TGATTCCTAGATTCC	1102
rs550910874	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522460	AATGAATGAATGAAT[A/G]TGGCTTTGTTATTCT	1102
rs551018325	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531691	TTACCTGCTGCTTAA[C/T]AACACGCATGTACTG	1102
rs551048528	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524480	CAGTAACGTGACCAA[C/T]AGTCACCAACCAATC	1102
rs551186650	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48496781	GAGGGGAAGGGAGGG[A/G]AGAAGAGAAGAGGGG	1102
rs551386879	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48490690	AAGAAAAAGGTAAGC[C/T]ATAAAAAGCAGTAAT	1102
rs551425601	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496690	GCTGTAAGAGTGCCC[A/G]CCGTGAAAAGAAAGA	1102
rs551444788	snp	C/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48504421	GGCTTTCTCATTGAC[C/T]TTCAATGACTTCATA	1102
rs551588601	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489091	AAGAATCTGAGACTA[C/T]GTTCCATTTCAGTTT	1102
rs551638840	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516074	GCTGTGGAAACTAGG[C/T]TGGTTGTAAAAGCAA	1102
rs551713341	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517605	GCAGCTGTCCCAATG[C/G]CCACTGGACCTAAAG	1102
rs551735695	in-del	-/A	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48523990	AAATGTAAGATTAAC[-/A]TAATTTCATATTTGT	1102
rs551785170	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516995	TCTTTCCCATCAGTT[A/G]TTAAATCAACCTTAC	1102
rs551824337	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48524483	TAACGTGACCAATAG[A/T]CACCAACCAATCAGT	1102
rs551869709	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513825	TTCTGGTTCCCATTC[A/G]TGGTACCTTGTTTCC	1102
rs552175525	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529043	AGTACAAAGCAAAGC[A/G]GTATTTAATTGAAAA	1102
rs552184644	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48492694	TGTTTCGCTTTCTTT[C/G]CCAGCCTGCAGGAAA	1102
rs552192536	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530398	AGTATTTGTAATCTA[C/T]GTAAGTAAAGGACAT	1102
rs552312848	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518994	ATAATGTCTATATCT[C/T]ATATCTTATTTCTGA	1102
rs552379635	snp	A/C	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48522684	AAAATAAATAAAAAT[A/C]AAATATTCTCTCTCC	1102
rs552470971	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527949	CTGTACATATTATTT[C/G]TGGCAAAGTAATCAG	1102
rs552561997	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494103	ATCTTTCCAAGCTTC[A/C]GTTTTCTCATTTATA	1102
rs552601053	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501690	TTGGACACTTAGAAT[A/G]TAATTGTTGAACGAA	1102
rs552626411	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501550	ACGCCTATGGTACTG[A/G]TTCCCGGAACCACAC	1102
rs552630700	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532336	AAAACGGCTTCGCCT[A/C]ACAAAGTCAAACTTT	1102
rs552673749	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501482	CACACTTGGAGCGTG[C/T]GCTGGCTGCTCCCTG	1102
rs552778420	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493406	TCCTCAACACAGCAG[C/T]CAGGAGGCAGGAGGA	1102
rs552779893	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501427	CAGAAACGGTAACTG[A/G]TGGACGTCCAAGTAT	1102
rs552838944	snp	A/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48493227	TAAGTACCCTCCTTC[A/T]CACACACACACACAC	1102
rs552846869	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506853	ATTTTTTGGAATCAT[C/T]TCTGTGTCCTTTGGG	1102
rs552862042	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48520311	GACCCAATCAACTCC[A/G]TGCCCAACTGTCAAG	1102
rs553055343	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492639	AGTCCTCGTGCAGAC[A/G]TGCCAGCAGCATCTG	1102
rs553102487	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512664	ATTGTATTTCCAGGA[C/T]TACTATAGAAGTCTA	1102
rs553141161	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519679	CATTCTCTTCAAGGA[A/G]GTCACAATTTAATAG	1102
rs553226144	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508464	CCCAGGCTAGAGTGC[A/G]GTGTCGCGATCTCAC	1102
rs553297002	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530407	AATCTATGTAAGTAA[A/G]GGACATGAGGGGAAA	1102
rs553297134	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521135	TTTTGTAGGACTCTC[A/G]AGTTCTATACATTAC	1102
rs553366374	in-del	-/CA	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48490740	AAGTCATTAACAGGC[-/CA]CACCGCTTTTTCTCT	1102
rs553494427	snp	A/C	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48517260	CCATGTCATCCATCC[A/C]TTGAAAGGAGCTAAC	1102
rs553528179	in-del	-/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48519863	ATTTATAAAATGCAT[-/G]TATTTGCATTTTTTG	1102
rs553533993	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532494	CAGAAATGAAAACAT[C/T]GGCAACATATGCAGT	1102
rs553737556	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48525985	GAGGGAATACCAAAG[A/G]TAAAAGGTCCCATGT	1102
rs553812612	in-del	-/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48524084	AAAAAGTGTTTTGAA[-/T]TTTTTTAGCATTGTG	1102
rs554013845	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48512277	TTTCCTCTCAAAGTG[A/C]TTCACATTCATAAAT	1102
rs554066945	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533168	CGGGTGCCCGGCCGA[A/G]ACGGAAACGAAGGGA	1102
rs554190983	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526834	GGCAAGAGAATCACT[G/T]GAACTTGGGAGGCAG	1102
rs554363143	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505384	AATTCAAATTAGTAC[A/G]ACTTTCCCTAGAAGA	1102
rs554434880	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533698	TGATTATATTTTGCA[A/G]TAATTTATTATATTA	1102
rs554468441	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48499131	ACACACACACACACA[C/T]ACACACACACACTCT	1102
rs554474256	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48517986	AAGAAGGCCAGATGA[C/T]AACAGACACAGGGAC	1102
rs554503594	snp	A/G	1.64784e-05	0.00287035	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512110	GTGACTCTTCGAGGG[A/G]TTGGCTGATTAACTG	1102
rs554608601	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48525612	TTTCCAGATCACTAA[C/G]AAGTCCTGCAATTTT	1102
rs554682436	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499231	TTTTTAGCCAAGCTA[C/T]GGCCCTCTGGAAATG	1102
rs554778780	snp	C/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48511242	AAGCAGTTCTGTATC[C/T]TGCTTCATTTTACCA	1102
rs554817596	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48532741	GCGCACCGGGCCCAC[C/G]CCAGCGGAATTGCGC	1102
rs554967277	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48519781	GGCTGGCTGTTGGAA[A/G]TTAGTCATCAAAGAC	1102
rs555005571	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527414	AAAGGTGCTTTGTTC[C/T]TTGCAAAACAGTCTC	1102
rs555020722	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48504767	AGACCCCACTGACAC[A/G]GGCTAGCACCTGAAG	1102
rs555039670	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513378	CCATGTACTACTACT[C/T]AAGTCAAGAAATATA	1102
rs555093589	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521003	TTGTATATATATTTG[C/T]ATATGTTCAATCACT	1102
rs555130508	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520462	GCACAGGTAACCTTC[C/T]TTACTGCAAATAACA	1102
rs555240592	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491294	TACATATAAACCTAC[A/G]GTACATTTTCTTTTA	1102
rs555367553	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48523375	TTTCAAATTCTGCCT[C/T]ATATGACAGTTATTC	1102
rs555436757	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48506956	AGCCAAATAATGCGG[C/T]TCTTATGTTCCCTTC	1102
rs555463336	snp	C/G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48498124	AAAGGGTAACCTGGG[C/G/T]TGGGGGTGGATAGAG	1102
rs555633660	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509948	GAAAAGATAGTGAAA[C/T]GTTTTTGCTCTACAC	1102
rs555818636	snp	C/T	3.29565e-05	0.00405921	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490078	CTTTTGCAGGGGAAA[C/T]GGAAAGGCTCAAAAA	1102
rs555882827	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517080	TCTGAACACCTACTT[G/T]TCCCTTCCACCTTAG	1102
rs556040164	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48510512	AGGAATAAATACTCT[C/T]GTTAAATAATATTCT	1102
rs556087576	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524805	AGAGAAAAACAGAAG[A/G]AAAAGAATATACTGT	1102
rs556126254	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532464	TATGGGACGGGAGCC[C/T]AGGGGTCGAGGCCAC	1102
rs556129438	in-del	-/CTTT	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48524112	GTGGGAGATGGTTGG[-/CTTT]TTTTTTTACATTATT	1102
rs556132273	snp	A/G			synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490237	GCAAAACCTGAAGCA[A/G]AATTCTTCTAAATCC	1102
rs556179166	snp	C/G	1.65381e-05	0.00287555	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490251	AGAATTCTTCTAAAT[C/G]CTAGGAACAACAACA	1102
rs556193623	in-del	-/CTC	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48531066	TTCCCTTTCTCTGTT[-/CTC]CTTTTTCATTTTTTC	1102
rs556223220	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531985	GTTAAACAGTGTCTG[A/G]GGGAAAGAGCAACGA	1102
rs556281821	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48517805	TTGAATGGCTTCCCC[C/T]CAAAGTCCAAATCCA	1102
rs556283636	snp	A/G	1.64917e-05	0.00287151	intron-variant	RCBTB2	GRCh38.p7	13:48510591	TTAATCACAATCACC[A/G]AAGACCAGTGTGGGG	1102
rs556310709	in-del	-/AT/ATAT	0.204032	0.25836	intron-variant	RCBTB2	GRCh38.p7	13:48527320	TATATGACTTGGCTC[-/AT/ATAT]ATATATATATATATA	1102
rs556322398	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517167	CCTCCCCTGTCCTCA[C/T]TACCATGAATTTCTC	1102
rs556325681	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498930	CAACAAATCCCATCA[G/T]CAACCTCTTTAAAAT	1102
rs556435147	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503971	ACCCAGGGGAAGTCC[C/G]CATCTTGATTTTGCT	1102
rs556436529	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496377	CATCCTGATTTACAG[G/T]TGCTCACTCAGCCAC	1102
rs556499925	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488553	TGTAAACTATGGACC[A/G]TGGGTGATAATGATG	1102
rs556797301	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498207	GTCCTGCCTGTGCCA[C/T]TGGGTTCTGGCACAA	1102
rs556816566	snp	C/T	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48497495	ATTTGTTTTTCTGAA[C/T]CTTCATTACAGGATT	1102
rs556839346	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48500933	CTAAAATGCTGTGTT[A/G]AGTGTGTGACTCACT	1102
rs556951506	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501533	CTTTTCAAGCCTAAG[C/G]AACGCCTATGGTACT	1102
rs556988479	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507624	TGGAAAACCTTGAGG[A/G]GGGTGAAAGGTCATC	1102
rs557095329	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48522176	TGGATGGCCTCTTAC[A/G]GGAATCTTCCTGCTG	1102
rs557219849	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515432	CCAAACAGGAATCAT[A/C]TTCCTTAAGCAAACT	1102
rs557256932	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522871	GACAGATAAAAACAA[C/T]AATCAAAATACAGCC	1102
rs557275890	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530473	CCCTCTTTCTCTAAG[C/T]CTTCTTTAATTATGG	1102
rs557403314	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502966	CCGGGGCAGAAACAA[A/G]TTGGGTCCTCCTCCC	1102
rs557776474	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48495390	TACTTTTTCAAAAAA[C/T]AAAAATAGGATAAGT	1102
rs557788920	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502045	TCTGTAATCATTAAG[A/G]ATAAGAATCTCACAA	1102
rs557851383	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503774	GGTTGGTCTTGAACT[C/G]CAGAGCTCAAATGAT	1102
rs557893063	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501563	TGGTTCCCGGAACCA[C/T]ACAACCTGTGTTATT	1102
rs557943103	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508334	TGGTTGAAACTGTGC[A/G]AGTTCAGAAACCACC	1102
rs557953903	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488632	GGTGTTGACAGCAGG[G/T]AAGGCTGCGCATGTG	1102
rs558025504	snp	G/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48509873	ATTAAATATAATAAA[G/T]ATATATGCAGTAAAA	1102
rs558062368	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48509142	TACCAGCCTGGGCAA[C/T]GTGGCAAAACCCTGG	1102
rs558214575	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497290	CTCACTTACTTCCCA[A/C]AACCCCAGCCCCAGG	1102
rs558432271	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527316	TGGGATATATGACTT[C/G]GCTCATATATATATA	1102
rs558464905	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48516249	CTTCAGTTTAAGGAA[C/T]TGGTGGGTTTCCTCA	1102
rs558652296	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521073	AAACTATTCTTTATT[C/T]TATGAAAGCTGTTCC	1102
rs558728772	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526770	AAAATACAAAAATTA[A/G]CCAGGCGTAAGAGTG	1102
rs558742057	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48517174	TGTCCTCATTACCAT[A/G]AATTTCTCTGGGGCC	1102
rs558867557	in-del	-/A	0.0773238	0.180784	intron-variant	RCBTB2	GRCh38.p7	13:48522408	GATTTGCTAAGCTGG[-/A]AAAAAAAAAGGAGAA	1102
rs558923057	snp	A/G	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48520681	TTATTATTCCTTTGA[A/G]TGTGTGATACCTGTA	1102
rs558991499	snp	C/T	0.00398564	0.0444627	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504252	AGGTTAATCATCCTC[C/T]TGGAACACCGTTCTC	1102
rs559047217	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491997	TGCTACCACTCTGTA[C/T]GGCTTCATGTTCAAA	1102
rs559066081	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48527697	TTTCCTATTTCAGCT[A/G]TTTTCCTAATTGTAC	1102
rs559091129	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514567	AGGCCTAGGATAAAG[A/G]TGCCTTCCCCTAGAA	1102
rs559094917	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505771	TTCAAAGAAAAAAAA[A/T]GATGAGGGGGAACAG	1102
rs559222492	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500341	GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTTG	1102
rs559239164	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492572	ACTGCGCTAAAACTG[C/T]TTGCCAAGGCCCCTC	1102
rs559257368	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499546	CCTCACAGTGACTTT[A/C]TTTTAGGTTCTATAG	1102
rs559291545	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512251	CTGACATGTACTTGT[A/G]GCACCGAGTCTTTCC	1102
rs559586363	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48524128	TTTTTTTTTTACATT[A/G]TTTCAATGTGATGCA	1102
rs559597772	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48491561	ATTTTTAGAAATGAC[A/G]TTTTTGCCTACAGCA	1102
rs559736641	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501312	CTATAGACCTTTTTG[A/G]TCTGGAAAGGCCTTG	1102
rs559755839	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507838	CGTTAAGAACAAAGA[C/T]ACAAATGTTGGTCAA	1102
rs559863550	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512949	TCTACTTCATTATAC[A/G]AAAATATATGTAGCA	1102
rs559900189	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520002	ATGTTCATTAGAGCA[C/T]TTCAGATTTCAGGTT	1102
rs559937245	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532066	TAAGTCGCCAAGCGC[A/G]GTACAAAGTAGCTCC	1102
rs559998372	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48513240	AGGTCTTAATTTCCT[C/T]ATCTTTAAAATAATC	1102
rs560160674	snp	C/T	4.94222e-05	0.00497078	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510708	GCCCATAAGAATTGG[C/T]GCCCCAAGCATACAC	1102
rs560279628	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524197	ATAGTTTGTGCACTA[C/T]ACGTGGAGATTACCT	1102
rs560427951	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519095	AGACTAAGTAATCTT[C/T]CAAGATCACTAGCTT	1102
rs560442623	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516672	CAAATAAGTTGCACT[A/G]TGAGGTACTGGCTGT	1102
rs560536838	snp	A/C/T	1.65138e-05	0.00287343	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502859	TGTACACGTGCCCAC[A/C/T]CTGCGTCTTGGCCGC	1102
rs560591742	snp	A/T	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48518795	AGCTAAGGATGGAAT[A/T]TTGTTACGTTAGCTT	1102
rs560598325	snp	C/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533464	CCTTTTCCACAGCCC[C/G]TCTCCTCCAGCCTGC	1102
rs560643436	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490376	AAGTGGAGGAAATGA[C/T]GGCATGGTAATACCT	1102
rs560650277	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532785	CCTCTGCCTGCGGCC[C/T]GGGCTGGGTGTAGCC	1102
rs560682110	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48511601	GAAGAGAAATTTTCT[C/G]AACAGCTGCAATTTA	1102
rs560723562	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533267	CGCCCCTCCCCTTTC[A/T]CGCAGACGCCCCCTC	1102
rs560803633	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520608	ATTTTAATATTAGCT[C/T]AAGGAAAACATAATT	1102
rs560808806	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525597	ATCTCAGCCCACTAA[C/T]TTCCAGATCACTAAC	1102
rs560810450	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508367	TTGAAATTCAAGTAC[A/G]GAAAACAGAAAATCA	1102
rs560817038	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497945	TCTGCGCCTCCTCCA[C/T]GCACACCTTCAGCAC	1102
rs560820854	in-del	-/T/TT	0.337158	0.234315	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503544	TAATTCTCAGAACAA[-/T/TT]TTTTTTTTTTTTAAG	1102
rs560951535	snp	A/C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515830	AGAGGGCGAACACTG[A/C/G]TTTTGGGAGGAACAC	1102
rs560979087	snp	C/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48498520	CGGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA	1102
rs560989682	in-del	-/CAGCACTGT	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48521612	TAGCCTCTTGCAGGC[-/CAGCACTGT]CAGCACTGTCTGAAT	1102
rs561082892	snp	C/T	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48518404	TGGTTCTCCCATTCA[C/T]TTTTGAAACAGTGCT	1102
rs561088515	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48525476	TTCTTACTCCTCCTA[A/C]ATGAGATGCTTGATA	1102
rs561223304	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504344	CCATCCATGATTTGG[C/T]GTCACCTCTGTACAG	1102
rs561266212	snp	A/G	3.30579e-05	0.00406544	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510769	TGCGTAGCCACAGGC[A/G]ACCTGGAAGGAAAAA	1102
rs561267046	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519147	AAGCCCAGAGTTCTT[C/T]CCACATATCATCTGA	1102
rs561298956	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512282	TCTCAAAGTGCTTCA[C/T]ATTCATAAATCCTCA	1102
rs561301688	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534005	TGTTTCGTCTGGCTT[C/T]TGTCATTTCTTCGGA	1102
rs561544910	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533446	GTATGATGCTGAGAG[C/G]AACCTTTTCCACAGC	1102
rs561607924	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526937	TAATAATAATAAATA[G/T]ATTTTTTTTAAATAG	1102
rs561656418	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508751	AACTGCAGTTTAAGA[A/C]GACAGAAATGCAATA	1102
rs561684840	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516069	AAGTAGCTGTGGAAA[C/T]TAGGCTGGTTGTAAA	1102
rs561761820	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531652	GGAAGTGGGGTATGC[A/C]AGAACGTATCATTCT	1102
rs561810450	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509257	GCCTGAGCTTGGGAA[C/G]TCAAGACTACAGTGA	1102
rs561849307	snp	A/C	3.30715e-05	0.00406628	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515708	ACTTTCCCACATCTA[A/C]CATCTTCAAAGATGA	1102
rs562005114	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521738	CAGCATTCTCCATAC[C/G]CACAACGATTATCTG	1102
rs562027029	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48499851	CTCTCGAAGGTGCAC[A/G]CTGGCACGTCCCTGC	1102
rs562477655	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515821	TTCTGTAGAAGAGGG[C/T]GAACACTGGTTTTGG	1102
rs562567297	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530757	CCTTGTAAAAGTCCA[C/G]TGTCTTCATTTGATG	1102
rs562690057	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517572	TGCAGTCAGTAAAGG[C/G]AAGCTAGGATGCACG	1102
rs562728085	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520483	GCAAATAACACTACT[A/G]CAGGTGATAATTAAC	1102
rs562816235	in-del	-/ATA	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48499030	CACACCTGAACCAAT[-/ATA]ATAACTGATGTTTTA	1102
rs562823019	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489672	CATACTGAAGATTTA[C/T]AATAAATTGAGTGCC	1102
rs562848823	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48523519	AAGCATCCTTAGAAC[C/T]CAGCTTTTTGTATAC	1102
rs562884941	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525478	CTTACTCCTCCTACA[C/T]GAGATGCTTGATATC	1102
rs562886238	snp	A/C			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533650	AGTTACCTTGGGGCC[A/C]AGGGCTTCGAAAACA	1102
rs563001758	snp	C/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48532241	TTCAATGTCTGAAAA[C/G]CTCTATTTCCAGGGC	1102
rs563054725	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497732	TCTGCTAATAAATCT[C/T]ATACATGTGGTAGAC	1102
rs563255389	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48501161	ATGGGAATGTTCTCT[A/G]TCTGGATGTGGGGCA	1102
rs563435283	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529917	TATTTATGAGATGGG[A/G]TCTTACACTATTGCC	1102
rs563445445	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48492098	CATACTTCTCCCCAT[A/G]AGCCTGACATCTCCC	1102
rs563543828	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521367	ATAAGCAGATATTAT[A/G]TAAATTTAACAAAAT	1102
rs563657267	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502228	GCACAATGGCTCACA[C/T]CTGTGATCCCAACAC	1102
rs563743014	in-del	-/T	0.146985	0.227789	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535256	CTCCTATTCATCCTC[-/T]TTTTTTTTTTTTTTT	1102
rs563789225	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494697	CTTGACATCTGAGAT[C/G]GCCCTCCATCACCGT	1102
rs563818688	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501652	CTTACAATTTTTCTT[G/T]ATTACTGAGGTGCCT	1102
rs563856684	snp	G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48507953	TATGTAAACATAAAT[G/T]GCTGACAAATATCAG	1102
rs563873438	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507225	TGCAGTAGCTGCTAC[A/G]GGAATGAGAATGCAG	1102
rs563909206	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521598	ACATTGATCAACTCA[C/T]AGCCTCTTGCAGGCC	1102
rs563946249	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529967	GTGATCATGACTCAC[G/T]GCAGCCTCAACCTTC	1102
rs564083132	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492783	TGTCTCCTTATCTCC[C/T]TAACCTCTAAGCACA	1102
rs564197969	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531516	AAATAAAGTTCTGTG[C/T]CATGCAGATTTGCGA	1102
rs564352315	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508125	CCCACCCCACATTCA[A/G]TCCAGTTCCTAATTA	1102
rs564365127	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529099	CTTTTCAGCCACACA[C/T]GGCAAAAGTGTCATT	1102
rs564424619	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48493697	CTGATGTCTTGCCTC[C/T]CTGACCATTCTATTT	1102
rs564435657	snp	C/G	1.76961e-05	0.00297452	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502694	CCCAGATTTTCAGGC[C/G]ATCCCCCAAATGGAC	1102
rs564464637	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48496046	AAATACTTGCTTATA[C/T]GTTGTCTAGTACTCT	1102
rs564659465	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502293	GCCCACGGTTTAAGA[C/T]CAGCCTGGGCAACAC	1102
rs564711107	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48511482	GGTTCCTCAGGGAAA[C/T]TCCCTAGGAGTAGAA	1102
rs564770580	in-del	-/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48521372	CAGATATTATGTAAA[-/T]TTAACAAAATAACAC	1102
rs564785925	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504987	AGGAAAAAAAGGCTA[C/T]GATGGCCCACAGTGG	1102
rs564938488	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509540	ACAGCTGCAGGCATC[C/T]ACCTGCACCACCTCC	1102
rs564942245	in-del	-/TTGT	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48516320	AGAAAACACGTGTAC[-/TTGT]TTGTTAAGGCAGCCG	1102
rs565029685	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505660	GACATGGTCTGTCTT[C/T]GTGGCCTGGTGCTGT	1102
rs565110300	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48499841	CCACGTTCTTCTCTC[A/G]AAGGTGCACGCTGGC	1102
rs565137778	snp	A/C	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489347	AAGAAAAGCAAAGGA[A/C]CTTATGTGATTATGT	1102
rs565181746	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498662	TTGAAACCGGGAGGC[A/G]GAGGTTGTGGTGAGC	1102
rs565218599	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504936	ACTTATTATGAGGAT[A/C]GTTCTTAGCCCTTGA	1102
rs565230924	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48501191	AGTGGTTTCACAGGC[A/G]TAGACATGTGTCAGC	1102
rs565250155	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506634	AGGTGTGGGGGCCAA[C/T]GTACACATAGCTGAG	1102
rs565388470	in-del	-/ATC	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48527371	ATATTTATATATGAT[-/ATC]ATATATATATGATAT	1102
rs565409404	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500572	TCTAAAAAAAATAAG[A/G]TGGGGGGAAATTTGG	1102
rs565488847	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519862	AATTTATAAAATGCA[G/T]GTATTTGCATTTTTT	1102
rs565529435	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532989	ACGTCACGGCCGCGA[C/T]CCCCCTCGGCCTCCC	1102
rs565652205	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518780	CCAAGGCCACAATAG[A/G]GCTAAGGATGGAATT	1102
rs565818978	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489967	TAGGCAGACAAAGAC[C/T]ACTCACCACCATCCT	1102
rs565886236	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492437	AAAGTAAAGATGTTT[G/T]ACCTCAAATGCCCCA	1102
rs566240234	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506126	GGCCAGAGCCGTGGA[A/T]TAAGAGTCTGTGAGG	1102
rs566351006	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491724	CACAGATCTGGACAG[A/C]ATCAGGAAAATTGCT	1102
rs566360360	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501358	AACCATCTAAAAGTA[C/T]GCCACAAGTGATTAT	1102
rs566403717	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500138	TAAAAATTCCTGTGT[C/T]GAAGTCCTAATGGCC	1102
rs566438642	snp	A/G	1.68698e-05	0.00290424	stop-gained, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496265	CTTGCTTGATAGTTT[A/G]TTGGCAGAGCTTTTT	1102
rs566476166	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509811	AAATTAGAAAAGAAC[C/T]GCATATAAATGTGAG	1102
rs566484386	snp	A/G	3.29913e-05	0.00406135	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502829	TCACGGACTGACCCC[A/G]GCACTGGCCCCACAT	1102
rs566494285	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503775	GTTGGTCTTGAACTC[A/C]AGAGCTCAAATGATC	1102
rs566495377	snp	A/C	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48510924	CAACATCCTTCCAGA[A/C]CATGTGGGCCAGAAT	1102
rs566515088	snp	C/T	0.00398564	0.0444627	intron-variant	RCBTB2	GRCh38.p7	13:48527947	GTCTGTACATATTAT[C/T]TGTGGCAAAGTAATC	1102
rs566526439	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531709	CACGCATGTACTGTC[C/T]AGCAGGAAATAAAGA	1102
rs566531475	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48510478	ACCTCCCCAACAATT[C/G]CAAAGCCAATTTTTC	1102
rs566756972	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48517691	TTTCTATCTTTTCTG[A/C]ATAATCTTCATGGCA	1102
rs566820233	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509518	AAGCTACAAGATGTG[C/T]GAATGAACAGCTGCA	1102
rs567086969	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532335	CAAAACGGCTTCGCC[C/T]AACAAAGTCAAACTT	1102
rs567158242	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48516596	GACACCAATTATATT[A/G]GATTAAGGTCCACCC	1102
rs567206663	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489152	CTAAAAAGTACAAAT[G/T]TATCTCATTCTTGTT	1102
rs567451238	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48494294	CTTATTTGAGCCAGG[A/C]AAATCAAATACAGCA	1102
rs567460666	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509601	TGAAGGGGCCAGGGG[C/T]CTTAAATTTTAAGGT	1102
rs567595660	snp	A/T	0.000213133	0.0103209	intron-variant	RCBTB2	GRCh38.p7	13:48496329	TAGCAGTCCTGGCGG[A/T]AAGAGGTGTTTATTA	1102
rs567871871	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525834	CAAAATGATACATAT[A/G]GTATCATTTGATAAC	1102
rs567930238	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514898	GGGGGGATGTTGGAC[A/G]CAAGGTTTAGTCTTT	1102
rs568053175	in-del	-/CTCTCTCTCTCTCTCTCTCTCTCTCT			intron-variant	RCBTB2	GRCh38.p7	13:48499143	ACACACACACACACA[-/CTCTCTCTCTCTCTCTCTCTCTCTCT]CACACACACACACAC	1102
rs568276043	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529134	AATATGAAAAATAAC[A/C]AACATAAATGATAAA	1102
rs568297697	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48529170	TTTTAAGTTGTTATA[C/T]GCACTAATGTGAGTT	1102
rs568307384	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513919	TATACTGTTTTTCCC[C/T]ATACGTATATACTTA	1102
rs568366938	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530964	TTCTAAAACCCAGTT[A/C]CCCATGTTAAACATC	1102
rs568436839	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521646	GGGGATGGCCTTTGC[A/G]CCTCATCTGTCACTG	1102
rs568458978	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48496494	TGGGGCTCTACCCAG[A/G]ATGGCAGCCAAGCTG	1102
rs568482475	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494372	AGTCTATTTTACTTA[C/T]AGTCTATTATACTAA	1102
rs568580257	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48515939	CGAGCAGCGGAGGCC[C/T]GGATGGAACCAGGTC	1102
rs568603987	snp	C/T	3.56754e-05	0.00422332	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496199	TCCTTACCTGTGCAT[C/T]ATACTTCACCGCAGC	1102
rs568747075	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532566	TCCCTCGGGACCTGT[A/G]ACGCCCCCCCAGCCA	1102
rs568769568	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502022	TCCCCTGAAGACAGA[C/T]TTGCATCTCTGTAAT	1102
rs568805925	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502416	AAGGATCGCTTGAAC[C/T]CAGGGGCTGAAGGGT	1102
rs568892769	snp	A/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48509771	AATTTGGTTCTTCAT[A/T]TTCATTGTTAAGTAT	1102
rs569101915	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508305	CCCTCGGAATACGCC[C/T]GTGATTGAGTGCCTG	1102
rs569220927	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515044	TCCTAGATTCCATCT[A/G]CCACATCACCTTATG	1102
rs569245458	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503025	AAAATTACAAAAAGG[A/G]TCAGGAAAAGGAAAA	1102
rs569287175	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520069	AAATATTCAAAAATT[A/T]AAAAAAAAATCTGAA	1102
rs569295258	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512496	TAACCTCTTTACTAC[A/G]GCAACAGAGAAGGAA	1102
rs569334087	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519471	AAATGATTAGTTCTA[A/G]GCTTTCTTCCTGGCC	1102
rs569346078	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522882	ACAATAATCAAAATA[C/T]AGCCAAGTCTAAACA	1102
rs569384285	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531129	CAAATATGTTTTTTA[A/T]CATTCTTTGCTAGAA	1102
rs569452689	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513018	AAGCTAATCAACTTC[A/C]CCATTCCACCAAAGT	1102
rs569467000	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491626	CTTTGGCTGAAGTCT[A/G]CAGAGAGGAATGGAG	1102
rs569552454	snp	C/T	3.29516e-05	0.00405891	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490187	TCCATTTCTGCAAAA[C/T]CTGATGTTTGTGTTA	1102
rs569681978	in-del	-/T	0.242775	0.249896	intron-variant	RCBTB2	GRCh38.p7	13:48505051	TTTTTTATTTCTTTC[-/T]TTTTTTTTTTTTTTC	1102
rs569749781	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534482	CCATGGCAAGATCTG[C/T]TTGCCTTGCGCACTT	1102
rs569811682	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527165	AAGCTGGCAACAGTA[C/T]TGGGAAGATTTTCTT	1102
rs570095652	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513841	TGGTACCTTGTTTCC[G/T]TGCATAGCAAGCCCC	1102
rs570095675	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48508412	AAACATTCATCCATG[-/T]TTTTTTTTTTTTTTG	1102
rs570096959	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530081	TTGTTCGTTTTTCTG[C/T]AGAGACAGAGTTTTG	1102
rs570158835	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506773	GAAGATAAGCATTTA[C/T]GAACTGCTCTTCCTT	1102
rs570548477	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527992	TATCTGCTACACAAT[A/G]TGTTATATTACTCGG	1102
rs570684955	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503208	ATATGCACCATCCTG[C/T]TTTGAAATTCAAGTA	1102
rs570897034	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48514654	ATAAATTCAAGGGTT[A/G]AGATTTCTTGGACCG	1102
rs570929553	snp	A/T	0.0456336	0.143994	intron-variant	RCBTB2	GRCh38.p7	13:48493321	CACACACACACTCTC[A/T]CTCTCTCTCTCTCTC	1102
rs570983804	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48525201	TAAAACACAAAGAAA[A/G]GAGCAGTAAACTTGA	1102
rs571026297	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48499906	GCCAGGGTTTTCAAA[C/G]AATCATCTATTCAGC	1102
rs571106221	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503922	ATCAGAATAAGCCAC[C/T]ATACAGATTGAAGGA	1102
rs571158937	snp	C/T	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48494141	TCTAATATAATAATG[C/T]CTATGTCATATAAGG	1102
rs571217925	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525908	TATTTTAATGTGTTA[C/T]GGATACCAACATATG	1102
rs571254492	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532884	GGTCGCGGCTCTAGT[A/C]CCCTGGGCCCCTCAG	1102
rs571319941	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48517806	TGAATGGCTTCCCCC[A/C]AAAGTCCAAATCCAC	1102
rs571485021	snp	A/C	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48498048	TAATTGGCCTTGAGG[A/C]CACATGTGTGGGTAT	1102
rs571521582	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48499975	GGAAGCAGCCCCAAT[A/G]GCCGTGCTAATGGGG	1102
rs571525623	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48521123	TTCTGTTAACATTTT[C/T]GTAGGACTCTCGAGT	1102
rs571767297	snp	A/T	0.0142736	0.0832652	intron-variant	RCBTB2	GRCh38.p7	13:48518480	AAAAAAAAATATATA[A/T]ATATATATATATATA	1102
rs571851209	in-del	-/CACTAGGCTGCGTGACTAG	0.0138799	0.0821421	intron-variant	RCBTB2	GRCh38.p7	13:48505120	GAATCCTCGCTCTAC[-/CACTAGGCTGCGTGACTAG]CACTAGGCTGCGTGA	1102
rs571851335	snp	C/T	1.64874e-05	0.00287113	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511861	TGCCCGTTTCCGTTG[C/T]AACCCCAGACATAGA	1102
rs571898558	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524960	ATGTAACTTTAGAAT[A/G]TCATACTTTATAAGC	1102
rs571927987	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48511274	TACACATAGCAGTTT[C/T]CCATGTCATTAAAAA	1102
rs571937272	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532495	AGAAATGAAAACATC[C/G]GCAACATATGCAGTG	1102
rs572019641	snp	A/G	0.000675303	0.0183629	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510737	ACTTGGCCTTCATCT[A/G]TTAATACTAATGTGT	1102
rs572020585	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512314	AACACAGGCAGAGAA[G/T]TGTTTATAAAATGCA	1102
rs572208740	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504766	AAGACCCCACTGACA[A/C]GGGCTAGCACCTGAA	1102
rs572239977	snp	C/T	8.2494e-05	0.00642185	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515307	CAATGGTGCTCTGGA[C/T]GTCACCTAACCCCAA	1102
rs572264349	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520356	AGCAAGAGCCAAGTA[C/T]GGTCAAGAGAAAAAT	1102
rs572342386	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48494668	ATTCAGATGCAAACA[C/T]CACGTGCCACCATCT	1102
rs572461979	snp	A/G	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48527380	ATATGATATATATAT[A/G]TGATATATATTTATA	1102
rs572498235	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526840	AGAATCACTTGAACT[G/T]GGGAGGCAGAGGTTA	1102
rs572640701	snp	A/T	0.0505692	0.150756	intron-variant	RCBTB2	GRCh38.p7	13:48499140	CACACACACACACAC[A/T]CACTCTCTCTCTCTC	1102
rs572678690	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498452	ACTGCCACTCGCGGC[C/T]GGGCGCAGTGGCTCA	1102
rs572742308	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533975	ACATTCCAAACCACA[A/G]TGACCGTGTCAGTCT	1102
rs572866850	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531323	ATTTCTACAATTAAC[A/C]AATACCTTCTGAGCT	1102
rs572914780	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493780	TTACTTCTTTCCATA[A/T]CACTTGTCACCATCT	1102
rs572954560	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501565	GTTCCCGGAACCACA[C/T]AACCTGTGTTATTTC	1102
rs573059970	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502046	CTGTAATCATTAAGA[A/G]TAAGAATCTCACAAA	1102
rs573154350	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496479	ACTTACACTTCAGTG[C/T]GGGGCTCTACCCAGG	1102
rs573244002	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489304	ACATTGTCATTTTCA[C/T]TTACAGAGGCAAGTC	1102
rs573446135	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48525734	TAAACTGTGGCATAT[A/G]CATACTATATAGCTA	1102
rs573569058	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48492691	TCCTGTTTCGCTTTC[G/T]TTCCCAGCCTGCAGG	1102
rs573591790	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48531844	AGTAATGACATTGTT[A/G]GAAACTCTTCACAGT	1102
rs573676847	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48524095	TTGAATTTTTTAGCA[A/T]TGTGGGAGATGGTTG	1102
rs573715258	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48523442	TTCAAAAGGGCAGAC[A/G]ATTCCTTCATTGCTA	1102
rs573737700	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516466	CTGTGAGGGAAGGAT[C/T]TCTTCCAGGCTGTGC	1102
rs573854580	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531430	GAACCAGCAGTACAA[A/G]AGTTTGGAGAGCCAG	1102
rs573886741	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502535	GTCAAATAAAATTAC[G/T]TTTAGTTTAGTACTG	1102
rs574023153	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533060	CCTTGTCCGCTCCGC[A/C]TCCTGGGTAGCGGTT	1102
rs574088995	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532633	GAGCAGATGATCACC[C/G]TGGAACGACGCCAAA	1102
rs574161468	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503319	AAATAATAAAGATTT[A/G]GGTCATCTGGACTGA	1102
rs574220133	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493494	TTGGAACTCTGATTC[C/T]TGAAACTTGCCTATG	1102
rs574273295	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506354	AACTGCTTTGTAAAC[A/G]GGGCCATGATGTGAG	1102
rs574282862	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508583	TAATTTTTATATTTT[C/T]AGTAGAGACAGGGTT	1102
rs574293817	snp	C/G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503824	AGAGTGCTGGGATTA[C/G/T]AGGTGTGAGACACTG	1102
rs574435103	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506901	ATGTCAGTGACTGGA[C/G]CACAACAGCATCCTT	1102
rs574550943	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513270	CACCAAGTTGATTTT[C/T]AAAAATCTTTGTTAT	1102
rs574672737	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48512565	TACTACGTACAGGTA[A/G]ATGTCACAACATCAA	1102
rs574717733	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529630	TCCTGGAAACTTTCA[C/T]GTTGTTAGAATGTGA	1102
rs574740309	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48517768	GAAACCCGAAGAAAC[C/T]CCAGAGAGGAGCTGC	1102
rs574755483	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48508470	CTAGAGTGCAGTGTC[A/G]CGATCTCACTGCAAC	1102
rs574790251	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514713	ATCCATGGTTACAAC[C/T]TTTTGGGGAGAAGTT	1102
rs575167347	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48504770	CCCCACTGACACGGG[C/G]TAGCACCTGAAGGGT	1102
rs575271031	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530495	TAATTATGGATTGAA[A/C]TTTAGTTAGGTCTAT	1102
rs575271911	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48507132	ATGCTGCCCGTCCCG[G/T]GGCATGGCCTTGTGA	1102
rs575328527	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48501166	AATGTTCTCTGTCTG[A/G]ATGTGGGGCAGTGGT	1102
rs575368487	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506929	CTTCACTGATCTGCC[A/C]AACATCAGAAAAGCC	1102
rs575379149	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507674	GGAGAAGAAACAGCA[A/C]AGATGACAGATCCAC	1102
rs575428751	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514888	AAGAGTTGGCGGGGG[A/G]ATGTTGGACACAAGG	1102
rs575538454	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501537	TCAAGCCTAAGGAAC[A/G]CCTATGGTACTGGTT	1102
rs575761958	in-del	-/T	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48532686	CGCATGCGCAGCGCA[-/T]GCCTGGGCCGGCGGC	1102
rs575786117	in-del	-/A	0.00636936	0.0560724	intron-variant	RCBTB2	GRCh38.p7	13:48491244	GAAGATGGAAAAAAT[-/A]AAAAAAAATAGCAAT	1102
rs575826881	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48522182	GCCTCTTACGGGAAT[C/G]TTCCTGCTGAGGTCT	1102
rs575831553	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518109	AGCATTGCCCTGATG[A/G]TGCCTTGATTTCAGA	1102
rs575864546	in-del	-/CAAAGGCTTTCAAAAATAT	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48510020	ATGCTTGAGAAATTC[-/CAAAGGCTTTCAAAAATAT]CAGAATAACGTGGAA	1102
rs575865264	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530427	ATGAGGGGAAACACA[C/T]TTTACTTTCTAAAAT	1102
rs575866963	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526216	GAAAACTCATAAACT[A/G]TAATTTCTTTAGCCA	1102
rs575874411	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48517995	AGATGACAACAGACA[C/T]AGGGACTGCAGTAAT	1102
rs575927945	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489622	TGAAAGTTATTCCTT[C/T]TCCCAGTATTCCATG	1102
rs575931497	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505634	AAGTTACAAGCAAAT[A/G]TGAGGATAGCGACAT	1102
rs575940521	snp	C/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48504482	GCCTTACAAACCCTA[C/T]CCATCTTGTAAGGCC	1102
rs576208077	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48520068	AAATATTCAAAAATT[-/A]AAAAAAAAAATCTGA	1102
rs576251405	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499294	CAGACTTGACTGACT[C/G]AGGCCCACAGTCTGA	1102
rs576419507	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48528453	ATTATCCCATCTGGG[G/T]GGGTAACACATTTGA	1102
rs576434010	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48512658	CAAATGATTGTATTT[C/G]CAGGACTACTATAGA	1102
rs576497694	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535072	TTATTAATTTTTGTA[C/T]CATTAATTTTTGGAT	1102
rs576504500	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520530	TTACTACTTTTCTCA[C/T]ATCTAGTCCACCTCC	1102
rs576504671	snp	C/G	0	0	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512844	CCATGATTAGTTGTC[C/G]CATTGCCCAGCTGGC	1102
rs576624614	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512240	TCAACTGGACACTGA[C/T]ATGTACTTGTGGCAC	1102
rs576687312	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505688	TGTGGGCAGGACACG[C/T]GGATCAGAGTCAGAG	1102
rs576748621	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500295	CAGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA	1102
rs576918855	snp	C/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48500880	GAGAGAGTGAGCAAA[C/T]GCTGCACAGCTTGAT	1102
rs577078904	snp	C/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48529482	CTCCTACTGGTACTT[C/G]TTAGCTCAAAACATC	1102
rs577168514	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48518940	AAGAACAAGGTTTAG[A/G]AAGTGGAACAAGTAT	1102
rs577184717	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521099	GTTCCTAGGAAAAAT[C/T]AGGAATTTTTCTGTT	1102
rs577307200	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534056	ATAACTGCCTTTCTG[C/T]TACATAGGGCAGACA	1102
rs577326706	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513505	CAGTTTGTACTCATT[C/T]CATCTGTATTTTCCA	1102
rs577378836	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48492601	TCCGGCGTTCTCATC[A/G]CCAAACCCACTCGTC	1102
rs577588633	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490956	TCTCTTGATTAGAAC[C/T]ATAACTTGAAAATCA	1102
rs577598017	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48524874	TACAGCTTAAAAATT[A/G]TATCTGTGCTATCTA	1102
rs577643597	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48526477	GGATGTGGAGGCTGC[A/G]GTGAACCATGATCAC	1102
rs577704902	snp	G/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488922	TGACATTTTATAATT[G/T]TGCTGCTGTTTTGGG	1102
rs577770694	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48496434	GATATAATCCTCAGT[A/G]AAGCACTGCATAGAC	1102
rs577829699	snp	A/C	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48532465	ATGGGACGGGAGCCT[A/C]GGGGTCGAGGCCACA	1102
rs578041403	in-del	-/A	0.0138799	0.0821421	intron-variant	RCBTB2	GRCh38.p7	13:48518458	TACAGAGTACTTTGC[-/A]AAAAAAAAAAAAAAA	1102
rs578064861	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533842	AAATGCTCAACAATT[A/T]AATGTTATTAGCTAT	1102
rs578093815	snp	A/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533210	AGGAGGGGGCTGGCG[A/T]CGGCGTCTCGCCCCT	1102
rs578100424	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48504599	TTACTTTATGCATCC[A/G]TTTCACCTGTTCAGC	1102
rs578114714	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497848	CTTGAGTTGTGAATG[C/G]CTTCATTGTTTTTGG	1102
rs578200975	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48533009	CTCGGCCTCCCACAC[C/T]ACTCCTCCACCCTCT	1102
rs578254011	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505130	TCTACCACTAGGCTG[C/T]GTGACTAGCACTAGG	1102
rs578262515	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498278	GTCCTTTCAGTTCTT[A/T]ATGAAATTACATTTT	1102
rs745417753	snp	C/T	1.66291e-05	0.00288345	intron-variant	RCBTB2	GRCh38.p7	13:48511967	ATACTGGCATGAGAC[C/T]GATGTGGCAAACACG	1102
rs745474766	snp	C/T	1.65184e-05	0.00287384	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501789	GTACTTTCCATCAAC[C/T]AGAAACTTCAGGTCT	1102
rs745475203	snp	A/T	1.64776e-05	0.00287028	stop-gained, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512102	GGCAGCCAGTGACTC[A/T]TCGAGGGATTGGCTG	1102
rs745560562	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48506716	AAGCCATCTGGCATT[C/T]TCTGGGAGCAGGGGA	1102
rs745636711	snp	A/G	1.6799e-05	0.00289814	intron-variant	RCBTB2	GRCh38.p7	13:48515174	GCAGCTGCGAATAAA[A/G]CTGAAATTCTACATG	1102
rs745668478	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514684	GTTCAGTCTTGATGT[A/G]AATTAAACTACAAAT	1102
rs745736570	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48496154	CCTGGGTTCCATTTC[C/T]CCAGGAGGCCGGCAG	1102
rs745739033	snp	C/T	1.65149e-05	0.00287353	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521909	TAACCTTGCCACTGT[C/T]TCCAGAGAAAAGAGG	1102
rs745771434	snp	A/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502502	CATCTTTCTCTCTTA[A/G]AGAAAAAAAAAAAAG	1102
rs745808066	snp	C/T	1.67329e-05	0.00289243	intron-variant	RCBTB2	GRCh38.p7	13:48490289	TTTAATAAATTCATA[C/T]TTACTAATTCAATGC	1102
rs745862975	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48527915	TTCATTTGCCTGTAC[A/C]AAAGATATAACAGGC	1102
rs746024144	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48504972	ACCCAAAAATACTAG[A/G]GGAAAAAAAGGCTAC	1102
rs746220788	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531206	GCATCCCAAGCATCA[A/G]GGACAGGACGTGATA	1102
rs746270915	snp	C/G/T	4.94836e-05	0.00497391	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515300	CGAGGTTCAATGGTG[C/G/T]TCTGGACGTCACCTA	1102
rs746310495	snp	A/G	1.66454e-05	0.00288486	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515602	TCATCATTTACTGTA[A/G]TGTATAAAACTTCAT	1102
rs746344771	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48511233	ATGTTGTATAAGCAG[C/T]TCTGTATCTTGCTTC	1102
rs746528727	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48497646	TTTCATGCAAGGTAC[G/T]TAATAGAGTGTACGA	1102
rs746580633	snp	A/G	3.29685e-05	0.00405995	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511836	GTTGCCACTGTTGCC[A/G]AGTCCAAGCTGCCCG	1102
rs746597518	snp	A/G	4.95757e-05	0.00497849	intron-variant	RCBTB2	GRCh38.p7	13:48521980	GAGGAAAAAGTATGT[A/G]GTAAAATCAGGATCC	1102
rs746726966	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508184	AGAGTCAGAAGTAAG[A/G]CTCCGGGGTTCCCCA	1102
rs746729869	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48515500	TTTTTTTTTTAACCT[A/T]TTATTCCTTAGTTCC	1102
rs746807066	snp	A/G	1.66145e-05	0.00288218	intron-variant	RCBTB2	GRCh38.p7	13:48512703	TATTGAAAAAAATCA[A/G]TGAGCTTTATGCTGA	1102
rs746852001	snp	C/T	1.6477e-05	0.00287024	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512832	CAGGGCACTAAACCA[C/T]GATTAGTTGTCCCAT	1102
rs746907039	snp	G/T	1.64955e-05	0.00287184	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502819	TGCGGGAGGATCACG[G/T]ACTGACCCCGGCACT	1102
rs746907551	in-del	-/CATT			intron-variant	RCBTB2	GRCh38.p7	13:48508401	ACATCTCATTTAAAA[-/CATT]CATCCATGTTTTTTT	1102
rs746914957	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514883	ATGCTAAGAGTTGGC[A/G]GGGGGATGTTGGACA	1102
rs746957948	snp	A/G	1.6569e-05	0.00287824	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502879	GTCTTGGCCGCAGAC[A/G]TGTGTGTGGAGTGAC	1102
rs747078617	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48513069	TTGGAAAGTATAAAC[G/T]GCATTCTACCTCAAA	1102
rs747137204	snp	C/G	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510648	CCTTTTCCACAGTGA[C/G]AGGAGTAGGATAGGA	1102
rs747158518	snp	C/T	8.82278e-05	0.00664124	intron-variant	RCBTB2	GRCh38.p7	13:48515555	CCATTTCTAAAAATG[C/T]GAGTAGCTGATTTAT	1102
rs747198457	snp	C/T	1.64757e-05	0.00287012	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510724	GCCCCAAGCATACAC[C/T]TGGCCTTCATCTGTT	1102
rs747209338	in-del	-/AC			intron-variant	RCBTB2	GRCh38.p7	13:48499113	GACCCCCACCCCAAC[-/AC]ACACACACACACACA	1102
rs747226257	snp	C/G			utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533122	AGTTGGCGCCTCCCC[C/G]TGAAACGGCCCGGCC	1102
rs747237054	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526017	ACTCTGTCAATGAAT[C/T]GGTATGCTACAGCTT	1102
rs747251462	snp	C/T	1.70295e-05	0.00291796	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496238	GAGCGATGGCATTCT[C/T]CTCGCAGATGCCTTG	1102
rs747274459	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48511568	TTTATATTCCAAAAG[G/T]TATGTGACAGTGCCC	1102
rs747306542	snp	A/G			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488842	TATGAGACTTTATCC[A/G]AGTAACTGCTTGATA	1102
rs747324839	snp	A/G	3.29891e-05	0.00406122	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499743	TTATCTTCCAATGAC[A/G]AACGAAAATGCTCAC	1102
rs747381728	snp	G/T	4.96718e-05	0.00498331	intron-variant	RCBTB2	GRCh38.p7	13:48511920	CTCAAGAGACAAATG[G/T]CCAGCAAGCTGTCTG	1102
rs747436932	snp	C/T	3.30349e-05	0.00406403	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501782	CATAAATGTACTTTC[C/T]ATCAACTAGAAACTT	1102
rs747439267	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520363	GCCAAGTATGGTCAA[A/G]AGAAAAATCTGTATG	1102
rs747453879	snp	A/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501735	TCTCAAATAAATGAT[A/T]CCTTACCGAATCTTG	1102
rs747495145	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48531359	TATGGTGGAGATAGA[G/T]TGATCATACCCTTAC	1102
rs747607880	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518834	GCTTCTACTTTAAAT[C/T]ACCCCACCACCCAAT	1102
rs747653932	snp	A/G	3.29962e-05	0.00406165	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502807	AAGTGGGTGAGGTGC[A/G]GGAGGATCACGGACT	1102
rs747737655	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509646	GTTTTATTTAACCTA[C/T]AAAATTAACCTATGT	1102
rs747749577	in-del	-/CTT			intron-variant	RCBTB2	GRCh38.p7	13:48514744	TTATTTATTTTCTTC[-/CTT]TTTTCCTCCTTGCTT	1102
rs747765264	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48527719	TAATTGTACGGTTCA[C/T]TAATTTATTTTTAAA	1102
rs747858819	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48498911	CACCTCTCATCCCAT[C/G]TATCAACAAATCCCA	1102
rs747961856	snp	C/T	1.64803e-05	0.00287052	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512120	GAGGGATTGGCTGAT[C/T]AACTGTTGATCCAGA	1102
rs747971721	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48506326	TTTGATCTGATGTGA[G/T]AGGCAAATGGGAAAC	1102
rs747995394	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48516945	ATCAACAAACTTACA[C/G]ATTATTTAAAGCAAC	1102
rs748015096	snp	C/T	1.66896e-05	0.00288869	intron-variant	RCBTB2	GRCh38.p7	13:48512686	AGAAGTCTACATAAT[C/T]TTATTGAAAAAAATC	1102
rs748022601	in-del	-/CAA			intron-variant	RCBTB2	GRCh38.p7	13:48507535	CCTTGAGGGAATGAT[-/CAA]CAACAACTGCTGAGC	1102
rs748081682	in-del	-/A	3.31225e-05	0.00406941	intron-variant	RCBTB2	GRCh38.p7	13:48510779	AGGCGACCTGGAAGG[-/A]AAAAAAATCCACTCA	1102
rs748093373	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534241	GCCCCAAGTTTCTCC[A/G]CTGGTTACATCTTAT	1102
rs748166780	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507981	CAGTATTCTCCATCA[C/T]AAATAAAATCTTTTT	1102
rs748183062	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532230	CTTGGAAAGTTTTCA[A/G]TGTCTGAAAACCTCT	1102
rs748259602	snp	A/G	1.67607e-05	0.00289483	intron-variant	RCBTB2	GRCh38.p7	13:48515180	GCGAATAAAGCTGAA[A/G]TTCTACATGGGGTTC	1102
rs748459132	snp	A/T	1.69591e-05	0.00291191	intron-variant	RCBTB2	GRCh38.p7	13:48511764	ACAAACTGACAGTGG[A/T]CGTACCCTCTGGACA	1102
rs748596986	snp	C/T	1.6486e-05	0.00287102	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511829	TTGGCTGGTTGCCAC[C/T]GTTGCCGAGTCCAAG	1102
rs748597545	snp	A/G			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488953	ATTAAAAAAAACCCC[A/G]ACACATTTGTTCTGT	1102
rs748614214	snp	G/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499717	CACTCATTTCTACAA[G/T]ATCATCCTCGTTATC	1102
rs748622434	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48516338	TTGTTAAGGCAGCCG[-/T]TAACAAAGTAGTGAC	1102
rs748671461	snp	A/C	3.30415e-05	0.00406444	stop-gained, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501768	AAGGACTTTATGTGC[A/C]TAAATGTACTTTCCA	1102
rs748677180	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48490343	ACAAGTTAGGCAAAG[A/G]AAAAGGATTTAATAG	1102
rs748708963	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48520833	TTACGTTAGGCATAC[C/G]TAGCAAAAAAGAGTT	1102
rs748798725	snp	C/T	1.69836e-05	0.00291402	intron-variant	RCBTB2	GRCh38.p7	13:48512208	AGTAAATGAAACAGA[C/T]TAATTTATAAACTGT	1102
rs748858195	snp	C/G	1.71796e-05	0.00293079	intron-variant	RCBTB2	GRCh38.p7	13:48501907	CCAGAGTTAGCTACA[C/G]ACATAATGAACACAC	1102
rs748911366	snp	C/T	3.36967e-05	0.00410454	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502743	GGAGAGGAGGCGCCA[C/T]GTGACGGCGGGCGTG	1102
rs748982174	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48517139	CTCAAGTCCACACTA[C/T]TAACTTAGTAAGCCT	1102
rs748995890	in-del	-/A	0.000166834	0.00913175	intron-variant	RCBTB2	GRCh38.p7	13:48512692	TACATAATCTTATTG[-/A]AAAAAAATCAATGAG	1102
rs749014039	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48531114	TTCTAACCTAATATA[A/C]AAATATGTTTTTTAT	1102
rs749034201	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531180	GATCTTTGTCTCTTT[C/T]GTTCATTGATGCATC	1102
rs749060065	snp	C/T	0.000186411	0.00965249	intron-variant	RCBTB2	GRCh38.p7	13:48532996	GGCCGCGATCCCCCT[C/T]GGCCTCCCACACCAC	1102
rs749077973	snp	G/T	1.65113e-05	0.00287322	intron-variant	RCBTB2	GRCh38.p7	13:48496152	CACCTGGGTTCCATT[G/T]CTCCAGGAGGCCGGC	1102
rs749083993	snp	C/T	1.64781e-05	0.00287033	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510632	TGCCCGTGTTACCTG[C/T]CCTTTTCCACAGTGA	1102
rs749098998	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490136	AAGGCTCCAACTCTG[C/T]TTGCTTTGCTGATAA	1102
rs749181464	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48506543	GAGAGGAGCGGAAGG[A/T]GGCCCAGGGGATGAG	1102
rs749343265	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520894	GTACTTCCTAGCATT[A/G]TAACACTTCATATAT	1102
rs749370767	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533882	GTAAGCTACTTGCTT[C/T]TATACTGGCTGTTTC	1102
rs749459044	snp	C/T	3.29685e-05	0.00405995	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512868	AGCTGGCTATAAGCA[C/T]TATGACCCCAGGTAA	1102
rs749478396	snp	A/T	1.68923e-05	0.00290618	intron-variant	RCBTB2	GRCh38.p7	13:48515748	CTGTACTGGCTGAAA[A/T]GGAAAAAATATATGT	1102
rs749521035	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503707	GTGCAAGCCACCACA[C/T]CTGACTAACTTTTGT	1102
rs749616924	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48525242	AAATATGCCACAGAA[G/T]GGGGGAAGATATTTG	1102
rs749650732	snp	C/T	0.00018143	0.00952271	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515636	CAGCACTGCCAAAGA[C/T]ACAAGCCTGACGAAT	1102
rs749657316	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499273	AGCCTCCTAAGCCAC[C/T]GGGCACAGACTTGAC	1102
rs749702173	snp	A/G	3.31181e-05	0.00406914	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515716	ACATCTAACATCTTC[A/G]AAGATGACAGAGTAG	1102
rs749721215	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508499	ACCTCCACTTCCTGG[A/G]GTCAAGGGATTCTCG	1102
rs749750721	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48522289	GACTTCCTGTGATAA[A/G]GAAAAATAAATTTTA	1102
rs749754946	snp	C/T	3.71837e-05	0.00431167	intron-variant	RCBTB2	GRCh38.p7	13:48511744	AGACTTAAAAATACA[C/T]GCACACAAACTGACA	1102
rs749770514	snp	C/T	1.78595e-05	0.00298822	intron-variant	RCBTB2	GRCh38.p7	13:48496336	CCTGGCGGAAAGAGG[C/T]GTTTATTAGGGGGAG	1102
rs749881887	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489866	TCAAAAAGAGGAAAT[A/G]GTAAATAAGATATTT	1102
rs749885879	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520695	AGTGTGTGATACCTG[C/T]ATAACTATGCTTCTC	1102
rs750003950	snp	A/G	1.76204e-05	0.00296814	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496210	GCATCATACTTCACC[A/G]CAGCCGAGAGCAGAG	1102
rs750008195	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48494591	AACAGAGAGCTGGAA[A/G]GTAGCCAGACAAATA	1102
rs750042165	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532006	AGAGCAACGATCCAG[A/G]GCACTGTTTGTGAAC	1102
rs750056868	snp	C/T	1.68792e-05	0.00290505	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496267	TGCTTGATAGTTTGT[C/T]GGCAGAGCTTTTTCA	1102
rs750079349	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503446	TACCACACTGGGCTG[C/T]ATGACCTGGAGCCCA	1102
rs750081177	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48510126	AAATCTTAATTTCCT[A/G]ACCATTTTACTCTTC	1102
rs750095567	in-del	-/TTTACG			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534503	TTGCGCACTTGGTCT[-/TTTACG]CATTATGGACAGCTG	1102
rs750113256	snp	A/G	1.67823e-05	0.0028967	intron-variant	RCBTB2	GRCh38.p7	13:48512189	CCTGTTTAAAGGAAA[A/G]ATCAGTAAATGAAAC	1102
rs750125885	snp	A/G			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488641	AGCAGGGAAGGCTGC[A/G]CATGTGTAGGGCATG	1102
rs750184084	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519678	TCATTCTCTTCAAGG[A/G]GGTCACAATTTAATA	1102
rs750190692	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48498540	GTTCAAGACCAGCCT[C/G]ACCAACACGGAGAAA	1102
rs750254178	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528618	CCAAATATATCCTTA[A/G]GTGAGTCATTAGATA	1102
rs750287913	snp	A/G	1.65321e-05	0.00287502	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515341	GCCACAGCAGTTTGT[A/G]CCAAGCACAAAAATC	1102
rs750290708	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508069	TAGACAGATTTCTCC[C/T]TCCCACTTCTGTGAA	1102
rs750307766	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48521792	TGAGCCCCTCAAAGA[C/T]AGATAGTATCTCATT	1102
rs750378452	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497489	GATCCTATTTGTTTT[C/T]CTGAATCTTCATTAC	1102
rs750394006	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48509057	TGGGCCAGGCCAGGC[A/G]CAGTGGCTCATACCT	1102
rs750492268	snp	C/T	1.65258e-05	0.00287448	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515702	TTGGCCACTTTCCCA[C/T]ATCTAACATCTTCAA	1102
rs750543544	snp	C/T	1.65307e-05	0.0028749	intron-variant	RCBTB2	GRCh38.p7	13:48521864	TTTCATGCAACAGAA[C/T]ACACATGCTCCAAGG	1102
rs750546921	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48517694	CTATCTTTTCTGAAT[A/T]ATCTTCATGGCACTA	1102
rs750559630	snp	A/C/T	9.94471e-05	0.00705086	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511786	CTCTGGACACGGATG[A/C/T]CTTGCAAAGCTGCCA	1102
rs750591693	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48495250	TAAAAGTTAAAAAAA[A/T]ATAAGCAAAGAGAAG	1102
rs750614464	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499661	GATGCTGTCTGTGTA[C/T]AGGTATTCCAGGAAG	1102
rs750667269	in-del	-/A	0.0773238	0.180784	intron-variant	RCBTB2	GRCh38.p7	13:48522407	GATTTGCTAAGCTGG[-/A]AAAAAAAAAAGGAGA	1102
rs750884086	snp	C/G	1.64751e-05	0.00287007	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512788	CAACTTCAATGACTT[C/G]TTTGTTTGACAGATT	1102
rs750912603	snp	A/G	3.30398e-05	0.00406434	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502782	GGCAAACACGTCGTC[A/G]GTGCAGGAGAAGTGG	1102
rs750975764	snp	A/G/T	3.35995e-05	0.00409864	intron-variant	RCBTB2	GRCh38.p7	13:48512916	AATAAAAAGAAAGAC[A/G/T]ATCAGTTTTTTACAA	1102
rs750977967	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48526688	GGGAGGCAGAGATGG[C/G]AGGATTAATTGAGGT	1102
rs751073850	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489516	CTTTTGTCAATTCTA[A/C]ACAATGTTCTAAATT	1102
rs751189331	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48532608	GGAGCTTAGGATGAG[A/C]GCGGCCTCCGAGCAG	1102
rs751216685	snp	C/T			missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510698	GTGCCCAACTGCCCA[C/T]AAGAATTGGCGCCCC	1102
rs751242574	snp	G/T	5.33092e-05	0.00516253	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496204	ACCTGTGCATCATAC[G/T]TCACCGCAGCCGAGA	1102
rs751279205	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530579	AGGTGATTTAAGCTC[C/T]TCTCCTACACAGTTT	1102
rs751426979	snp	A/C	1.66175e-05	0.00288244	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501733	ATTCTCAAATAAATG[A/C]TTCCTTACCGAATCT	1102
rs751455901	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510697	AGTGCCCAACTGCCC[A/G]TAAGAATTGGCGCCC	1102
rs751466644	snp	C/T	1.6486e-05	0.00287102	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515235	CAATATGTGGACCAC[C/T]CCCATAGCTGAGGCA	1102
rs751471830	snp	A/G	3.37445e-05	0.00410744	intron-variant	RCBTB2	GRCh38.p7	13:48515157	AAACAATGTTCTCAA[A/G]GGCAGCTGCGAATAA	1102
rs751547854	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48500145	TCCTGTGTTGAAGTC[C/T]TAATGGCCAATACCT	1102
rs751556062	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48529885	ACAATTTTAATCTGT[A/G]GCAATATTTATTTAT	1102
rs751609304	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48522008	TCCCTTATGTTCGAT[A/G]GAACCAGGCAGGTTA	1102
rs751626100	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48497209	CTCCTCAGTTCTCTA[C/G]GCTGGATCATTTTTC	1102
rs751637258	in-del	-/AT			intron-variant	RCBTB2	GRCh38.p7	13:48515100	TATGGTATCCAAAAC[-/AT]AGTCAATTTCACAGG	1102
rs751695939	snp	A/G	6.59914e-05	0.00574381	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515686	GAACAAAGGGAAAAA[A/G]TTGGCCACTTTCCCA	1102
rs751714059	snp	C/T			missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496201	CTTACCTGTGCATCA[C/T]ACTTCACCGCAGCCG	1102
rs751823880	snp	C/T	1.70845e-05	0.00292267	intron-variant	RCBTB2	GRCh38.p7	13:48515764	GGAAAAAATATATGT[C/T]GAAATGACAAATTAA	1102
rs751876684	in-del	-/A	6.62306e-05	0.00575421	intron-variant	RCBTB2	GRCh38.p7	13:48499767	GCTCACATCTGAAGG[-/A]AAAAAAGCAGTATGT	1102
rs751891029	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503515	ACTGCTCTAAGTTCA[C/T]GATTGATGAGGAGGT	1102
rs751906706	snp	C/T	8.23811e-05	0.00641746	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512082	CACAACTACTTTATT[C/T]TGTAGGCAGCCAGTG	1102
rs751963548	snp	C/G	0.000639386	0.0178685	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533133	CCCCCTGAAACGGCC[C/G]GGCCTCGGCGGGATG	1102
rs751986284	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532770	GCATGCGCAGGGCCG[C/G]CTCTGCCTGCGGCCT	1102
rs751997266	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514347	GATGGTGAAATATCA[C/T]CCTACTCAGAATGGC	1102
rs752020037	snp	A/G			missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490148	CTGCTTGCTTTGCTG[A/G]TAAAGTTCTTCAGGA	1102
rs752185444	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48521699	TCTTAACCTGAGGTA[-/T]TATCAGTTTCCTGCT	1102
rs752225177	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48500214	GGTAATCAAGTTATA[A/C]GAAGGTCACTAGGGT	1102
rs752247822	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48512315	ACACAGGCAGAGAAG[G/T]GTTTATAAAATGCAT	1102
rs752293048	snp	A/G	2.56164e-05	0.00357876	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502954	TAAGCACAGTGACCG[A/G]GGCAGAAACAAGTTG	1102
rs752330564	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48523207	CTATGGCATCTTAGC[A/C]GATCTGTTAAAATCC	1102
rs752432426	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519060	CCTCATGTTACCTAT[A/G]AGGAAACTGGGGCAC	1102
rs752592900	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48530808	TCCTGAATAATTTGA[A/G]CTCTTATTTAGGAAA	1102
rs752603374	snp	C/T	1.74017e-05	0.00294967	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496312	TAAAATGTAGCCAAG[C/T]CTAGCAGTCCTGGCG	1102
rs752621866	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48501244	AATGCACACAGCTCA[C/T]TGCTCAAAAACATTC	1102
rs752656426	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499653	GAAAGGCTGATGCTG[C/T]CTGTGTATAGGTATT	1102
rs752806665	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48515430	ATCCAAACAGGAATC[A/C]TCTTCCTTAAGCAAA	1102
rs752807712	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529425	GCATAATACAGGACA[C/T]ATTATAATGCAGTCA	1102
rs752838739	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48521530	ATGAATTGAGAACAT[A/G]TCATCTAAGATCAGA	1102
rs752843934	snp	A/G/T	5.02932e-05	0.00501443	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501866	TGAGGTGGTCATCAG[A/G/T]TTCTAGGAGAATAAT	1102
rs752994469	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48522120	GCATGGGAATGAACA[C/G]CTATAAAACTCCAAA	1102
rs753026315	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48501129	AGGGCTAGGACATGA[-/G]GGGTCTTTGAAGGGT	1102
rs753049400	snp	A/G	1.65206e-05	0.00287403	intron-variant	RCBTB2	GRCh38.p7	13:48521967	CTGGGCAGTCCCTGA[A/G]GAAAAAGTATGTGGT	1102
rs753057734	snp	A/G	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490216	TACTACAGTCAGATG[A/G]TTTATGCAAAACCTG	1102
rs753097118	snp	A/C			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534537	TGAAGTTCATGCAGG[A/C]CTTACGGTGTGCTTC	1102
rs753108578	snp	A/C	1.65307e-05	0.0028749	intron-variant	RCBTB2	GRCh38.p7	13:48511895	GAGAGAAAATGAGAC[A/C]CTCAATCCTCTCAAG	1102
rs753115853	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48492619	AAACCCACTCGTCAG[C/T]TCTCAGTCCTCGTGC	1102
rs753180653	snp	G/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503525	GTTCACGATTGATGA[G/T]GAGGTAATTCTCAGA	1102
rs753188321	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533752	TAGATTTAAGTAAAA[C/T]GCACCACAACTTTGC	1102
rs753199814	in-del	-/TCTTCTCTTTCTT	1.69637e-05	0.00291231	intron-variant	RCBTB2	GRCh38.p7	13:48501883	CTAGGAGAATAATGC[-/TCTTCTCTTTCTT]AAATGCTTCCAGAGT	1102
rs753264710	snp	C/T	3.2956e-05	0.00405918	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512063	TCTGCCCACATGCTA[C/T]GGTCACAACTACTTT	1102
rs753298687	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531735	AAAGAGATTACGTTT[C/T]ACCTAGAATACTCAT	1102
rs753365749	in-del	-/C			intron-variant	RCBTB2	GRCh38.p7	13:48513852	TCCTTGCATAGCAAG[-/C]CCCCCCTTATCTGCA	1102
rs753453182	snp	A/C			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488518	CTCACAGAATGTGCA[A/C]CACCAACAATGGACC	1102
rs753454259	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514272	AACTAACGGGTGGGA[A/G]TGTCTATGGCAGAGA	1102
rs753491514	snp	A/G/T	3.29512e-05	0.00405891	stop-gained, synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512816	ATTAGTAGAGATATG[A/G/T]CAGGGCACTAAACCA	1102
rs753542670	snp	A/G	1.65026e-05	0.00287246	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502800	GCAGGAGAAGTGGGT[A/G]AGGTGCGGGAGGATC	1102
rs753588936	in-del	-/CAGTAAGG			intron-variant	RCBTB2	GRCh38.p7	13:48493204	CTTACTGGATTATAC[-/CAGTAAGG]AGCCTCCTAAGTACC	1102
rs753625922	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48507956	GTAAACATAAATTGC[G/T]GACAAATATCAGTAT	1102
rs753723897	snp	C/T	1.64914e-05	0.00287149	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515658	CTGACGAATTAACTG[C/T]AGTTCTTCTTCAGAA	1102
rs753729963	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510718	ATTGGCGCCCCAAGC[A/G]TACACTTGGCCTTCA	1102
rs753765212	snp	C/T	0.000292894	0.012098	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496226	CAGCCGAGAGCAGAG[C/T]GATGGCATTCTCCTC	1102
rs753765582	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48532540	GGAGGGAGAAACTTC[A/T]GGCAGGACGCTCCCT	1102
rs753811771	in-del	-/TTC	1.64917e-05	0.00287151	cds-indel, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515661	ACGAATTAACTGTAG[-/TTC]TTCTTCAGAACAAAG	1102
rs753818965	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48520337	TCAAGTAAGAAACTG[A/G]CTGAGCAAGAGCCAA	1102
rs753820917	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507194	AAGTCAGGGGTGGGG[C/T]GCGGATTTGGTTGGC	1102
rs753902748	snp	C/T	1.64933e-05	0.00287165	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511814	CCACTCTGCAAGGGG[C/T]TGGCTGGTTGCCACT	1102
rs753944522	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48504874	AGCTTGTACCGGCTC[A/G]CCTCAGAGGCTGAGA	1102
rs753959378	snp	A/C/G	4.96589e-05	0.00498271	missense, stop-gained, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501743	AAATGATTCCTTACC[A/C/G]AATCTTGAGAAGGAC	1102
rs754012315	snp	C/T	1.65111e-05	0.0028732	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512022	CTTCCTTACCTCCCC[C/T]GTGTCTACTACTGCC	1102
rs754065188	snp	A/G	4.99513e-05	0.00499731	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501854	ACTCAGCCACTGTGA[A/G]GTGGTCATCAGGTTC	1102
rs754071058	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529738	ATTATCAATATCCCT[C/T]ACCAGGAGGCAAGCC	1102
rs754127440	in-del	-/AGGCAAACACGTCGTCAGTGCAGGAGAAGT	1.65789e-05	0.0028791	cds-indel, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502766	CGGGCGTGGCAAAGC[lengthTooLong]GGGTGAGGTGCGGGA	1102
rs754161013	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516753	CATTAAGATCACGAG[C/T]ACCCACACTCCTATA	1102
rs754226027	snp	C/T	1.65263e-05	0.00287452	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502867	TGCCCACCCTGCGTC[C/T]TGGCCGCAGACGTGT	1102
rs754276039	snp	C/T	4.95774e-05	0.00497858	intron-variant	RCBTB2	GRCh38.p7	13:48521873	ACAGAACACACATGC[C/T]CCAAGGGCATGATTT	1102
rs754306557	snp	C/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535016	TCTTCCTTACAGTCT[C/G]AAGGTTTTCACTCAG	1102
rs754309549	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48527093	GGTCTAAATCTGCTT[A/G]CAAATGTCCCCCCTT	1102
rs754310994	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491486	TATACATAAAAATGT[A/G]CTTCAATGATACATG	1102
rs754340220	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48523529	AGAACCCAGCTTTTT[G/T]TATACTGGAACTGGC	1102
rs754459823	in-del	-/AAT			intron-variant	RCBTB2	GRCh38.p7	13:48514229	GAAACCAAGAGAGTC[-/AAT]CTAATAACTGAGACA	1102
rs754464278	snp	A/G	3.47023e-05	0.00416533	intron-variant	RCBTB2	GRCh38.p7	13:48512222	ATTAATTTATAAACT[A/G]TCTCAACTGGACACT	1102
rs754541097	snp	A/T	0.000197671	0.00993963	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510702	CCAACTGCCCATAAG[A/T]ATTGGCGCCCCAAGC	1102
rs754559055	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508301	CCCTCCCTCGGAATA[C/T]GCCCGTGATTGAGTG	1102
rs754652712	in-del	-/A			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503713	CCACCACACCTGACT[-/A]AACTTTTGTATTTTT	1102
rs754745959	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530673	GACATTTAGAAGCAA[C/T]TGCAAAAACTGTGGA	1102
rs754765254	snp	A/G	1.71846e-05	0.00293122	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496227	AGCCGAGAGCAGAGC[A/G]ATGGCATTCTCCTCG	1102
rs754789539	in-del	-/CCCTCTCTCTCTCTC			intron-variant	RCBTB2	GRCh38.p7	13:48493275	CTCTTCTCTCTCTCA[-/CCCTCTCTCTCTCTC]CACACACACACACAC	1102
rs754800740	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510721	GGCGCCCCAAGCATA[C/T]ACTTGGCCTTCATCT	1102
rs754824760	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48500155	AAGTCCTAATGGCCA[A/G]TACCTCAAAATGTGA	1102
rs754958429	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48527200	GTGACAGTGTTACAG[C/T]ATAAGATCATCTCAT	1102
rs754967057	in-del	-/AAGAATTGGCGCCCC	1.64732e-05	0.0028699	cds-indel, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510699	TGCCCAACTGCCCAT[-/AAGAATTGGCGCCCC]AAGCATACACTTGGC	1102
rs755031449	snp	A/G	1.65176e-05	0.00287376	intron-variant	RCBTB2	GRCh38.p7	13:48511890	GACCTGAGAGAAAAT[A/G]AGACCCTCAATCCTC	1102
rs755048501	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48514381	CAATTTAAAACTTAT[G/T]AATTGTTTATTTTGG	1102
rs755180123	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48495426	ACTTAGTGATATATC[C/T]TGAATAGCTGCATAA	1102
rs755222249	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497293	ACTTACTTCCCAAAA[C/T]CCCAGCCCCAGGGTT	1102
rs755225417	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526160	ATCATTCTAATTTTG[C/T]CTTTACCAAGGACAT	1102
rs755322511	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533683	CACCTTCTCCCCTTA[C/T]GATTATATTTTGCAG	1102
rs755329040	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532771	CATGCGCAGGGCCGC[C/G]TCTGCCTGCGGCCTG	1102
rs755350514	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48490287	GGTTTAATAAATTCA[A/T]ATTTACTAATTCAAT	1102
rs755368514	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48527319	GATATATGACTTGGC[C/T]CATATATATATATAT	1102
rs755382725	snp	A/G	3.30437e-05	0.00406457	intron-variant	RCBTB2	GRCh38.p7	13:48521879	CACACATGCTCCAAG[A/G]GCATGATTTTTTTCT	1102
rs755417010	snp	G/T	1.64792e-05	0.00287042	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490068	TCATCTCTGGCTTTT[G/T]CAGGGGAAATGGAAA	1102
rs755501315	snp	A/G	1.65151e-05	0.00287355	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521948	CTTCCATATGGACTC[A/G]GTCCTGGGCAGTCCC	1102
rs755558328	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48530019	CTACAGCCTCCCAAG[A/T]ATCTGAAACTACAGG	1102
rs755578550	snp	G/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534508	CACTTGGTCTTTTAC[G/T]CATTATGGACAGCTG	1102
rs755646426	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48530895	TGCCGTGGGCTCCCA[G/T]AAAAGACATTGTAGA	1102
rs755663350	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48532751	CCCACGCCAGCGGAA[A/T]TGCGCATGCGCAGGG	1102
rs755664791	snp	G/T			missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512153	CTACCTGCCCAGAGT[G/T]ATTATAACCCCAGGC	1102
rs755798700	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48490478	ACATTCAAGTTCCTC[C/T]GCACTAACCTAGGTA	1102
rs755866193	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48493595	CAGCTACTTCCCTCC[C/T]CACTGTGCTCCCTCC	1102
rs755889413	snp	A/G	5.05941e-05	0.00502936	intron-variant	RCBTB2	GRCh38.p7	13:48512197	AAGGAAAGATCAGTA[A/G]ATGAAACAGATTAAT	1102
rs755943740	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507130	TGATGCTGCCCGTCC[C/T]GGGGCATGGCCTTGT	1102
rs755977341	snp	C/T	1.65326e-05	0.00287507	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515342	CCACAGCAGTTTGTG[C/T]CAAGCACAAAAATCT	1102
rs756066707	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506440	CAAGGGAGAGAAAGA[A/G]TAGTCTGGAAGGCTG	1102
rs756066764	snp	A/G	1.68525e-05	0.00290275	intron-variant	RCBTB2	GRCh38.p7	13:48490301	ATATTTACTAATTCA[A/G]TGCAACATAGCATGA	1102
rs756086520	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48515509	TAACCTTTTATTCCT[C/T]AGTTCCCCCAAGATC	1102
rs756102973	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48492942	CTAATAGACATCACA[C/T]ACTTCTCATATTCAA	1102
rs756124628	snp	A/C	2.00254e-05	0.00316422	intron-variant	RCBTB2	GRCh38.p7	13:48511726	TGATATCTTTGCCAG[A/C]GAAGACTTAAAAATA	1102
rs756136509	snp	C/G	1.64746e-05	0.00287002	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510710	CCATAAGAATTGGCG[C/G]CCCAAGCATACACTT	1102
rs756141334	in-del	-/TCTCTCTCTT/TCTCTCTT			intron-variant	RCBTB2	GRCh38.p7	13:48493340	CTCTCTCTCTCTCTC[-/TCTCTCTCTT/TCTCTCTT]TTCTCTTCTCTCTCT	1102
rs756277325	in-del	-/ACC	1.69525e-05	0.00291135	intron-variant	RCBTB2	GRCh38.p7	13:48501885	AGGAGAATAATGCAA[-/ACC]ATGCTTCCAGAGTTA	1102
rs756300140	snp	C/T	0.00016472	0.00907375	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499670	TGTGTATAGGTATTC[C/T]AGGAAGGCCCGGTAA	1102
rs756352960	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48514569	GCCTAGGATAAAGGT[G/T]CCTTCCCCTAGAAAG	1102
rs756395731	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528583	AGACCACATAAATTT[C/T]AATAGGATAATGATG	1102
rs756445353	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48522171	ACTACTGGATGGCCT[A/C]TTACGGGAATCTTCC	1102
rs756453961	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48523232	AAATCCTAATTTTCT[C/T]TAAGACCCAGCATGA	1102
rs756514246	snp	C/T	3.38748e-05	0.00411537	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502738	CCCACGGAGAGGAGG[C/T]GCCACGTGACGGCGG	1102
rs756579638	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509659	TATAAAATTAACCTA[C/T]GTTAAATTGGTTAAA	1102
rs756613717	in-del	-/AAATG			intron-variant	RCBTB2	GRCh38.p7	13:48512975	TAGCACAGCTTCCAC[-/AAATG]AAATCTAAAAATTCA	1102
rs756620990	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48504855	GTGTTATCACAGAAC[C/T]TGGAGCTTGTACCGG	1102
rs756679140	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48491451	GAAAATTCACACACC[C/T]ACTTGTCATCACAGC	1102
rs756717347	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531930	AAACCCAGCAGGAAC[A/G]CAATACTAGGAAGGT	1102
rs756720227	snp	C/T	1.64757e-05	0.00287012	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490095	GAAAGGCTCAAAAAC[C/T]TTCCTGCAGATGGGA	1102
rs756778601	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519257	TTCTCAGACTCCTTA[A/G]GGAACAGGCAATAAT	1102
rs756780966	snp	G/T	3.33311e-05	0.00408221	intron-variant	RCBTB2	GRCh38.p7	13:48490276	ACAACAAAGATGGTT[G/T]AATAAATTCATATTT	1102
rs756826560	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489561	AGAATGATATACCAG[A/G]AGAATATGAACCTCA	1102
rs756837040	snp	G/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488582	TGTGTCCAAGCAGGT[G/T]CATCAGGTATAACAA	1102
rs756841818	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531141	TTATCATTCTTTGCT[A/G]GAATGTAAGCTCCAG	1102
rs756845273	snp	A/T	1.65244e-05	0.00287436	intron-variant	RCBTB2	GRCh38.p7	13:48521982	GGAAAAAGTATGTGG[A/T]AAAATCAGGATCCCT	1102
rs756940399	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48504537	GGTCTCCCGCTCACC[G/T]GAGCTCCTGCAGCAC	1102
rs756972614	snp	A/C/T	3.3122e-05	0.00406941	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501742	TAAATGATTCCTTAC[A/C/T]GAATCTTGAGAAGGA	1102
rs757005081	snp	C/T	3.37098e-05	0.00410533	intron-variant	RCBTB2	GRCh38.p7	13:48515166	TCTCAAGGGCAGCTG[C/T]GAATAAAGCTGAAAT	1102
rs757076388	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48497378	TTCAAGTAATTCAAC[A/G]TAGACTGGGTGAGGT	1102
rs757111197	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520377	AGAGAAAAATCTGTA[C/T]GGGGAAAAAAGCACT	1102
rs757143354	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48527843	CTGAACAAGGGGACA[C/T]TCTTTTGATAATGTG	1102
rs757154773	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48507249	AATGCAGAAAGTTTA[C/G]AGGGTACTTTCAGGT	1102
rs757240080	snp	A/G	1.76008e-05	0.0029665	intron-variant	RCBTB2	GRCh38.p7	13:48515558	TTTCTAAAAATGTGA[A/G]TAGCTGATTTATTTT	1102
rs757240548	snp	C/T	1.65946e-05	0.00288046	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502882	TTGGCCGCAGACGTG[C/T]GTGTGGAGTGACAGG	1102
rs757283732	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533911	TCATGAGGACACTGG[C/T]TCCTCTACAGTGTAG	1102
rs757285271	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510729	AAGCATACACTTGGC[C/T]TTCATCTGTTAATAC	1102
rs757296022	in-del	-/CT			intron-variant	RCBTB2	GRCh38.p7	13:48526003	AAAGGTCCCATGTAA[-/CT]CTGTCAATGAATTGG	1102
rs757366474	snp	A/T	1.64996e-05	0.0028722	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515687	AACAAAGGGAAAAAA[A/T]TGGCCACTTTCCCAC	1102
rs757380433	in-del	-/C	1.64955e-05	0.00287184	frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502836	TGACCCCGGCACTGG[-/C]CCCCACATGTACACG	1102
rs757511485	in-del	-/CTGT	1.65157e-05	0.0028736	frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521905	TTTCTAACCTTGCCA[-/CTGT]CTCCAGAGAAAAGAG	1102
rs757517192	in-del	-/A	0.000288265	0.0120021	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501700	AGAATATAATTGTTG[-/A]ACGAATTACTTTTCT	1102
rs757553067	snp	A/T	1.67928e-05	0.0028976	intron-variant	RCBTB2	GRCh38.p7	13:48510816	CAAATATAAGTAATT[A/T]TTTCACTGCTTCCAC	1102
rs757557711	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48524878	GCTTAAAAATTGTAT[A/C]TGTGCTATCTACTAT	1102
rs757583679	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48510939	ACATGTGGGCCAGAA[C/T]TGCAGTAAGATTGCC	1102
rs757609012	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48504927	ATCTCACTGACTTAT[C/T]ATGAGGATCGTTCTT	1102
rs757669201	snp	A/T	1.68832e-05	0.00290539	intron-variant	RCBTB2	GRCh38.p7	13:48501878	CAGGTTCTAGGAGAA[A/T]AATGCAAATGCTTCC	1102
rs757670679	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512085	AACTACTTTATTTTG[C/T]AGGCAGCCAGTGACT	1102
rs757725769	snp	A/T	3.34096e-05	0.00408702	intron-variant	RCBTB2	GRCh38.p7	13:48512181	GGCAAATACCTGTTT[A/T]AAGGAAAGATCAGTA	1102
rs757878290	snp	C/T	3.44364e-05	0.00414934	intron-variant	RCBTB2	GRCh38.p7	13:48512939	TTTTACAACATCTAC[C/T]TCATTATACGAAAAT	1102
rs757906491	snp	C/T	1.64947e-05	0.00287177	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502817	GGTGCGGGAGGATCA[C/T]GGACTGACCCCGGCA	1102
rs757928614	snp	A/C	1.64781e-05	0.00287033	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490081	TTGCAGGGGAAATGG[A/C]AAGGCTCAAAAACTT	1102
rs757931716	snp	A/T	1.65518e-05	0.00287674	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502875	CTGCGTCTTGGCCGC[A/T]GACGTGTGTGTGGAG	1102
rs757953809	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508157	TCAGGCTTTCCTGCA[A/G]TGGGCCGCAGAAGAG	1102
rs758000169	in-del	-/TTATCAATTTCAAGTAAAATTAAACTCTTTAAA			intron-variant	RCBTB2	GRCh38.p7	13:48523822	TCTTTTCAGTGTCTT[lengthTooLong]ATTAGAATGGTAGGA	1102
rs758001467	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48517914	TTAGAGTGGACCCTA[C/T]GTCCAATGACTAGTC	1102
rs758061307	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528637	AGTCATTAGATAGTA[C/T]CTTTAATAGCTTTTT	1102
rs758094119	snp	A/C/T	3.31649e-05	0.00407204	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511784	CCCTCTGGACACGGA[A/C/T]GCCTTGCAAAGCTGC	1102
rs758112881	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489974	ACAAAGACCACTCAC[C/T]ACCATCCTTCTTCTG	1102
rs758232663	snp	C/T	3.48778e-05	0.00417585	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496313	AAAATGTAGCCAAGT[C/T]TAGCAGTCCTGGCGG	1102
rs758235436	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529757	AGGAGGCAAGCCATC[C/T]ACTCCTTTGAAGTAA	1102
rs758249311	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48509075	GTGGCTCATACCTGT[A/C]ATCCCAGCACTTTGG	1102
rs758285958	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499657	GGCTGATGCTGTCTG[C/T]GTATAGGTATTCCAG	1102
rs758289973	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48515820	GTTCTGTAGAAGAGG[C/G]CGAACACTGGTTTTG	1102
rs758305677	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497520	AGGATTTGTAATTAG[C/T]ATAAAGAATGTCAGA	1102
rs758400430	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498574	CGTTTCTACTAAAAA[C/T]ACAAAATTAGCCAGG	1102
rs758401978	snp	C/G/T	4.9429e-05	0.00497116	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512829	TGACAGGGCACTAAA[C/G/T]CATGATTAGTTGTCC	1102
rs758406187	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48523717	CACTGCACTACCCTA[A/G]GCCCCCTTTCGTTCC	1102
rs758564078	snp	G/T	1.64855e-05	0.00287097	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515273	TTTTTGCCATTTAAA[G/T]AATCCAGTCTCCGAG	1102
rs758566434	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48495256	TTAAAAAAAAATAAG[C/G]AAAGAGAAGAAAATA	1102
rs758675710	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48506251	ACGCCGGGATCGGAG[G/T]GCAATGAGGCTTGCC	1102
rs758699035	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502598	ATTAGTTCCCTTTTG[C/T]AGAAGCCCATCAGAG	1102
rs758701227	in-del	-/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501450	CAAGTATCAATACAG[-/T]TGTTCAGAGCACAGG	1102
rs758737276	snp	A/C	1.65209e-05	0.00287405	intron-variant	RCBTB2	GRCh38.p7	13:48521973	AGTCCCTGAGGAAAA[A/C]GTATGTGGTAAAATC	1102
rs758757333	snp	C/G	1.66871e-05	0.00288847	intron-variant	RCBTB2	GRCh38.p7	13:48515389	TTAGTTCAAGCAGTT[C/G]TATTTCTAACAAATC	1102
rs758784530	snp	A/G			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503715	CACCACACCTGACTA[A/G]CTTTTGTATTTTTTG	1102
rs758798728	snp	C/G	1.65351e-05	0.00287528	intron-variant	RCBTB2	GRCh38.p7	13:48511898	AGAAAATGAGACCCT[C/G]AATCCTCTCAAGAGA	1102
rs758871450	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526697	AGATGGGAGGATTAA[C/T]TGAGGTCAGAAGTTT	1102
rs758882050	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532090	TAGCTCCATGAAATG[C/G]GTTTTGTTATAGTCC	1102
rs758890195	snp	A/G	1.64779e-05	0.00287031	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512071	CATGCTATGGTCACA[A/G]CTACTTTATTTTGTA	1102
rs758962252	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499639	CTGCCTCCTCAGGAG[A/G]AAGGCTGATGCTGTC	1102
rs758965158	snp	C/T	1.6519e-05	0.00287388	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501775	TTATGTGCATAAATG[C/T]ACTTTCCATCAACTA	1102
rs759004791	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501572	GAACCACACAACCTG[C/T]GTTATTTCTTGTTTC	1102
rs759139205	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48491179	GCAATTACATATGAA[C/T]ATTACACACGATAGT	1102
rs759162964	snp	A/C	1.65334e-05	0.00287514	splice-acceptor-variant	RCBTB2	GRCh38.p7	13:48499761	CGAAAATGCTCACAT[A/C]TGAAGGAAAAAAGCA	1102
rs759199192	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534459	GATTAAGTTTCTTTC[A/G]TCAGCAACCATGGCA	1102
rs759261336	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48502072	ACAAATATCTGCTTA[C/T]AAATCTGGCAAAATA	1102
rs759311105	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48517162	GTAAGCCTCCCCTGT[A/C]CTCATTACCATGAAT	1102
rs759380543	snp	C/T	1.64917e-05	0.00287151	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515666	TTAACTGTAGTTCTT[C/T]TTCAGAACAAAGGGA	1102
rs759439957	snp	A/G	3.38949e-05	0.00411659	intron-variant	RCBTB2	GRCh38.p7	13:48515753	CTGGCTGAAAAGGAA[A/G]AAATATATGTTGAAA	1102
rs759484990	snp	A/G	3.32685e-05	0.00407837	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511779	ACGTACCCTCTGGAC[A/G]CGGATGCCTTGCAAA	1102
rs759501241	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48512262	TTGTGGCACCGAGTC[G/T]TTCCTCTCAAAGTGC	1102
rs759504798	in-del	-/CTCTCTCT			intron-variant	RCBTB2	GRCh38.p7	13:48493315	ACACACACACACACA[-/CTCTCTCT]CTCTCTCTCTCTCTC	1102
rs759559329	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48501105	TGACAGAAGGAGCTG[C/T]GGTCACCCAGGGCTA	1102
rs759636619	snp	C/G	0.000381316	0.0138026	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533082	GTAGCGGTTACTGCA[C/G]GGTCAGGGGCCCGGC	1102
rs759646007	snp	A/G	6.60295e-05	0.00574547	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512023	TTCCTTACCTCCCCC[A/G]TGTCTACTACTGCCA	1102
rs759653771	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507840	TTAAGAACAAAGATA[C/T]AAATGTTGGTCAATC	1102
rs759672923	snp	A/T	1.79803e-05	0.0029983	intron-variant	RCBTB2	GRCh38.p7	13:48496178	CCGGCAGCTGGAAGC[A/T]AGCTTTCCTTACCTG	1102
rs759681688	in-del	-/GG			intron-variant	RCBTB2	GRCh38.p7	13:48531911	ACTGTCTAGTAAGGT[-/GG]GTAAAACCCAGCAGG	1102
rs759696213	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48528489	CTTTTATAATCAAAA[C/G]AAACAGGAAATTAAA	1102
rs759699400	snp	A/G	1.66813e-05	0.00288797	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501857	CAGCCACTGTGAGGT[A/G]GTCATCAGGTTCTAG	1102
rs759700125	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48500928	TGAGACTAAAATGCT[-/G]TGTTGAGTGTGTGAC	1102
rs759701030	snp	A/C	1.64944e-05	0.00287175	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512146	CCAGATCCTACCTGC[A/C]CAGAGTTATTATAAC	1102
rs759869176	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508734	AATTATAATTCAAAA[A/G]TAACTGCAGTTTAAG	1102
rs759917353	snp	A/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499571	CTATAGAAACCACCT[A/T]GTCAGTTCCTCAACA	1102
rs759941944	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529382	TTGAGATTGGTTTTG[C/T]TCAGTATTATATACA	1102
rs759946938	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48517180	CATTACCATGAATTT[C/T]TCTGGGGCCACCTTC	1102
rs759960793	in-del	-/AGAGATATGAC	1.64754e-05	0.00287009	frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512807	GTTTGACAGATTAGT[-/AGAGATATGAC]AGGGCACTAAACCAT	1102
rs760018301	snp	A/G	3.29462e-05	0.00405857	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510657	CAGTGACAGGAGTAG[A/G]ATAGGACTGGTTGCT	1102
rs760120202	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498448	AAAAACTGCCACTCG[C/T]GGCCGGGCGCAGTGG	1102
rs760221417	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48490734	TGCTCTGAAGTCATT[-/A]ACAGGCCACCGCTTT	1102
rs760227756	snp	C/T	1.67719e-05	0.0028958	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515739	CAGAGTAGCCTGTAC[C/T]GGCTGAAAAGGAAAA	1102
rs760312636	snp	A/G	1.64931e-05	0.00287163	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499616	TGGAAGTCTTTGGCA[A/G]TTACCTACTGCCTCC	1102
rs760398315	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48521504	AAGAAAGAAATTAAA[C/G]AATGTCTATGATGAA	1102
rs760400332	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48532450	TGGGGTACTAGATTT[A/T]TGGGACGGGAGCCTA	1102
rs760425266	in-del	-/AC/ACACACACACACACAC			intron-variant	RCBTB2	GRCh38.p7	13:48499111	CCGACCCCCACCCCA[-/AC/ACACACACACACACAC]ACACACACACACACA	1102
rs760461548	snp	C/T	1.73165e-05	0.00294244	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502719	ATGGACAGTGACCAG[C/T]TTACCCACGGAGAGG	1102
rs760490368	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533229	CGTCTCGCCCCTCCT[C/T]TCCTCCCTAGGCTGC	1102
rs760775125	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48529738	TTATCAATATCCCTT[-/A]ACCAGGAGGCAAGCC	1102
rs760776228	snp	C/T	1.6513e-05	0.00287336	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521935	AGAGGAAGTTCTTCT[C/T]CCATATGGACTCAGT	1102
rs760777231	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48529523	AGATATACATAAGAG[A/T]TATTAGCTCAGGCCA	1102
rs760835231	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516609	TTGGATTAAGGTCCA[C/T]CCTAATGACCTCATC	1102
rs760835552	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48510540	TCTAACACTAGCAGT[A/G]CATTCCCCACCATTC	1102
rs760836522	snp	A/G	3.63009e-05	0.00426018	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502946	ACACCACATAAGCAC[A/G]GTGACCGGGGCAGAA	1102
rs760864772	snp	C/T	3.29935e-05	0.00406149	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511873	TTGTAACCCCAGACA[C/T]AGACCTGAGAGAAAA	1102
rs760923556	snp	C/T	1.65233e-05	0.00287426	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499758	GAACGAAAATGCTCA[C/T]ATCTGAAGGAAAAAA	1102
rs760945817	snp	G/T	0.0001882	0.00969869	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533053	GCCGGAGCCTTGTCC[G/T]CTCCGCCTCCTGGGT	1102
rs760949287	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48505531	CATTCTTTTCAACAA[A/C]TAAAGAAAATGGGAG	1102
rs760978362	snp	A/G	1.67609e-05	0.00289486	intron-variant	RCBTB2	GRCh38.p7	13:48512913	GAAAATAAAAAGAAA[A/G]ACAATCAGTTTTTTA	1102
rs761037414	snp	A/G	8.25089e-05	0.00642243	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502801	CAGGAGAAGTGGGTG[A/G]GGTGCGGGAGGATCA	1102
rs761053522	in-del	-/T	1.77448e-05	0.00297861	intron-variant	RCBTB2	GRCh38.p7	13:48515547	TGGCAAATCCATTTC[-/T]AAAAATGTGAGTAGC	1102
rs761079280	snp	A/G	4.94238e-05	0.00497086	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512805	TTGTTTGACAGATTA[A/G]TAGAGATATGACAGG	1102
rs761111975	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48506757	GCCCAATGAACAATG[G/T]GAAGATAAGCATTTA	1102
rs761183771	snp	C/T	3.32281e-05	0.0040759	intron-variant	RCBTB2	GRCh38.p7	13:48515197	TCTACATGGGGTTCC[C/T]AGGTTACCTGTTGTT	1102
rs761206965	snp	G/T	4.95487e-05	0.00497714	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502862	ACACGTGCCCACCCT[G/T]CGTCTTGGCCGCAGA	1102
rs761241604	snp	C/G			intron-variant, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517353	CAGATTCACAGCCCT[C/G]CTTTCCATCTCATCC	1102
rs761249482	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532667	GACCCCTACCAGAGG[A/G]CTCGCGCATGCGCAG	1102
rs761259919	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48521092	GAAAGCTGTTCCTAG[G/T]AAAAATTAGGAATTT	1102
rs761334314	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510700	GCCCAACTGCCCATA[A/G]GAATTGGCGCCCCAA	1102
rs761387256	snp	A/T	1.77621e-05	0.00298006	stop-gained, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496205	CCTGTGCATCATACT[A/T]CACCGCAGCCGAGAG	1102
rs761397314	snp	G/T	4.95381e-05	0.0049766	stop-gained, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510757	TACTAATGTGTGTGC[G/T]TAGCCACAGGCGACC	1102
rs761433878	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528195	CTTCTGTCCACATTA[C/T]CCCAACCCAATGGTA	1102
rs761565410	snp	A/G	1.65957e-05	0.00288055	intron-variant	RCBTB2	GRCh38.p7	13:48512000	TTTTAAACAAGATGT[A/G]AAATAACTTCCTTAC	1102
rs761590473	snp	A/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502437	GCTGAAGGGTACAGC[A/G]AGTTATGATTGCACC	1102
rs761597850	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48509031	AAGTGTAGGAGCACC[A/G]TAAAAAGTAATGGGC	1102
rs761846464	snp	C/G	0.000363108	0.0134693	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502855	CACATGTACACGTGC[C/G]CACCCTGCGTCTTGG	1102
rs761868318	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48521586	GGAATGGGATAAACA[C/T]TGATCAACTCATAGC	1102
rs761909708	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530599	CTACACAGTTTCAAA[C/T]ACAGAAAAGCAATGA	1102
rs761932042	in-del	-/C			intron-variant	RCBTB2	GRCh38.p7	13:48519019	TTCTGATCTTCACAA[-/C]AATTGTAGGACATAG	1102
rs761979718	snp	A/T	1.66607e-05	0.00288619	intron-variant	RCBTB2	GRCh38.p7	13:48512903	TTCTCCTTCTGAAAA[A/T]AAAAAGAAAGACAAT	1102
rs762001623	snp	C/T	1.71496e-05	0.00292822	intron-variant	RCBTB2	GRCh38.p7	13:48515769	AAATATATGTTGAAA[C/T]GACAAATTAAAAAGT	1102
rs762153997	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531435	AGCAGTACAAGAGTT[C/T]GGAGAGCCAGACATT	1102
rs762162769	snp	C/T	1.68664e-05	0.00290395	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496264	CCTTGCTTGATAGTT[C/T]GTTGGCAGAGCTTTT	1102
rs762195547	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526635	GAAAATAAAAATAGC[C/T]TGGGCGCGGTGGCTC	1102
rs762215652	snp	A/T	1.65214e-05	0.0028741	intron-variant	RCBTB2	GRCh38.p7	13:48496371	TTCAAGCATCCTGAT[A/T]TACAGTTGCTCACTC	1102
rs762280874	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48511469	TACAGGAATTGTTGG[-/T]TCCTCAGGGAAATTC	1102
rs762351623	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512775	TAAGACCCACAGGCA[A/G]CTTCAATGACTTGTT	1102
rs762357479	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491035	GTGCTGAGACCTCCA[A/G]TATGCCTCAAACCCT	1102
rs762364442	in-del	-/CAC			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488601	CAGGTATAACAAATG[-/CAC]CACTCTGGTGGGGGG	1102
rs762454053	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507439	GTCAGGATGTCTGGC[A/G]TATTTCACACTTTTA	1102
rs762484243	in-del	-/AG	1.64798e-05	0.00287047	frameshift-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490210	TGTGTTACTACAGTC[-/AG]AGATGGTTTATGCAA	1102
rs762485386	snp	A/G	1.64953e-05	0.00287182	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515226	TTGCAAGGACAATAT[A/G]TGGACCACTCCCATA	1102
rs762494909	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533568	GGGGCGGAAGTCTTG[C/T]AGCCCCCTGTAGTAC	1102
rs762532565	snp	A/G	2.65509e-05	0.00364345	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502956	AGCACAGTGACCGGG[A/G]CAGAAACAAGTTGGG	1102
rs762548844	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516157	AAGTCAAGAACAATG[C/T]TTGGTAAAGAACAAC	1102
rs762584285	snp	C/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534296	ACAGGTTTGCTCTCA[C/G]AAAAAGCTCACTTCA	1102
rs762752489	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48499920	ACAATCATCTATTCA[C/G]CAAGGCTGTATATAC	1102
rs762779680	snp	A/G	1.65141e-05	0.00287346	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521922	GTCTCCAGAGAAAAG[A/G]GGAAGTTCTTCTTCC	1102
rs762827230	snp	A/G	6.59381e-05	0.00574149	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511857	AAGCTGCCCGTTTCC[A/G]TTGTAACCCCAGACA	1102
rs762882328	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48492240	AGGCCTGTGGATGCA[A/G]TCTTCTCTGGATCAA	1102
rs762925298	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48522832	ATCTGGTATTTTCTA[C/T]AGTAGAGTGAGAGCC	1102
rs762962219	snp	A/G	1.64798e-05	0.00287047	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512742	ACCTCTCCATCAGAT[A/G]TTAGCACCAAAGAAT	1102
rs763014129	snp	C/T	1.65644e-05	0.00287783	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502769	GCGTGGCAAAGCAGG[C/T]AAACACGTCGTCAGT	1102
rs763017265	snp	G/T			synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510661	GACAGGAGTAGGATA[G/T]GACTGGTTGCTTTTA	1102
rs763053938	snp	A/C	1.6596e-05	0.00288058	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512168	TATTATAACCCCAGG[A/C]AAATACCTGTTTAAA	1102
rs763067208	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48518918	TTTTAAGTCTGTAAA[G/T]TTCCAAAAGAACAAG	1102
rs763087308	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48509731	CACAATACCCAAATG[-/A]AAACTGAGGCAGTTG	1102
rs763276960	snp	C/T	1.78784e-05	0.00298979	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496196	CTTTCCTTACCTGTG[C/T]ATCATACTTCACCGC	1102
rs763282151	in-del	-/AAG			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501374	GCCACAAGTGATTAT[-/AAG]AAGGTGATTATTAAG	1102
rs763333964	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48506953	AAAAGCCAAATAATG[C/T]GGTTCTTATGTTCCC	1102
rs763511519	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528332	GCAGAGAAGTCCCAG[C/T]ATTACATATTTTAAA	1102
rs763530192	snp	A/G	1.64925e-05	0.00287158	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515229	CAAGGACAATATGTG[A/G]ACCACTCCCATAGCT	1102
rs763605519	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48497993	ACATGCCCACTTCTA[A/G]ACCACACTTTGGGTA	1102
rs763619155	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48514244	AATCTAATAACTGAG[A/C]CAGCTACTAAGTAAC	1102
rs763648170	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531730	GAAATAAAGAGATTA[C/T]GTTTCACCTAGAATA	1102
rs763656816	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501406	GAGCTGAGCTTGATT[C/T]CCAGGCAGAAACGGT	1102
rs763679198	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489434	CATGTGAGAAATTAA[C/T]GAATGACTCCAAGTA	1102
rs763725636	snp	C/T	1.65021e-05	0.00287241	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515312	GTGCTCTGGACGTCA[C/T]CTAACCCCAAACAGC	1102
rs763755378	snp	C/T	1.64857e-05	0.00287099	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511858	AGCTGCCCGTTTCCG[C/T]TGTAACCCCAGACAT	1102
rs763774869	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510683	TTGCTTTTATTGCCA[A/G]TGCCCAACTGCCCAT	1102
rs763939800	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532528	GCGAGTGGGTTAGGA[A/G]GGAGAAACTTCAGGC	1102
rs763992626	snp	C/T	1.6884e-05	0.00290547	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501707	AATTGTTGAACGAAT[C/T]ACTTTTCTCAATTCT	1102
rs764020164	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48519090	CAGGGAGACTAAGTA[A/C]TCTTTCAAGATCACT	1102
rs764036089	snp	C/T	1.71705e-05	0.00293001	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502725	AGTGACCAGCTTACC[C/T]ACGGAGAGGAGGCGC	1102
rs764056654	in-del	-/CTAAAAGTACGCCACAAGTGATTATAAGAAGGTGATTATTAAGA	1.69706e-05	0.0029129	intron-variant	RCBTB2	GRCh38.p7	13:48501887	GAGAATAATGCAAAT[lengthTooLong]GCTTCCAGAGTTAGC	1102
rs764191422	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512771	ATGGTAAGACCCACA[A/G]GCAACTTCAATGACT	1102
rs764219681	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48516743	TAACAGCATACATTA[A/C]GATCACGAGCACCCA	1102
rs764246595	snp	C/T	3.30808e-05	0.00406686	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502775	CAAAGCAGGCAAACA[C/T]GTCGTCAGTGCAGGA	1102
rs764265075	in-del	-/AAATT	1.7169e-05	0.00292988	intron-variant	RCBTB2	GRCh38.p7	13:48515579	GATTTATTTTCTTCA[-/AAATT]ACCTCATCATTTACT	1102
rs764384214	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48494406	AGGGTACAGCAATTA[A/G]CTGGACAGGCTGTAG	1102
rs764395692	snp	C/G	1.64933e-05	0.00287165	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515674	AGTTCTTCTTCAGAA[C/G]AAAGGGAAAAAATTG	1102
rs764499371	snp	A/T	0.000238351	0.0109141	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533117	CGATGAGTTGGCGCC[A/T]CCCCCTGAAACGGCC	1102
rs764533700	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48508892	CTGCCCCAGTGAGAA[A/C]CTGAATCAGAAGCCT	1102
rs764653376	snp	C/T	1.64773e-05	0.00287026	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512072	ATGCTATGGTCACAA[C/T]TACTTTATTTTGTAG	1102
rs764720547	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533558	CCATTGCTGTGGGGC[A/G]GAAGTCTTGTAGCCC	1102
rs764740275	snp	A/G			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503299	AAAACATCACTTACT[A/G]AAGAAAATAATAAAG	1102
rs764780825	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48532683	CTCGCGCATGCGCAG[C/T]GCAGCCTGGGCCGGC	1102
rs764787521	snp	C/G	1.66228e-05	0.0028829	intron-variant	RCBTB2	GRCh38.p7	13:48499786	AAAGCAGTATGTCAG[C/G]TCCTAGCTTCCCAGC	1102
rs764865432	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489830	GAGACCAGGGTACCA[A/G]AGGTGTCCAATTTAA	1102
rs764868426	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48520536	CTTTTCTCACATCTA[G/T]TCCACCTCCCCTTCC	1102
rs764877998	snp	C/T	3.39986e-05	0.00412288	intron-variant	RCBTB2	GRCh38.p7	13:48515757	CTGAAAAGGAAAAAA[C/T]ATATGTTGAAATGAC	1102
rs764922275	snp	C/G	1.65181e-05	0.00287381	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515214	GGTTACCTGTTGTTG[C/G]AAGGACAATATGTGG	1102
rs764968989	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509056	ATGGGCCAGGCCAGG[C/T]GCAGTGGCTCATACC	1102
rs765062057	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498468	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	1102
rs765077403	in-del	-/CTCT			intron-variant	RCBTB2	GRCh38.p7	13:48493277	CTTCTCTCTCTCACC[-/CTCT]CTCTCTCTCCACACA	1102
rs765111223	in-del	-/TT			intron-variant	RCBTB2	GRCh38.p7	13:48524368	ACAGTAAAAATAAAG[-/TT]ATTCTGTGCCAGGCA	1102
rs765166829	snp	A/G	1.64928e-05	0.00287161	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512032	TCCCCCGTGTCTACT[A/G]CTGCCATGCAGCACA	1102
rs765302827	snp	A/G	6.59131e-05	0.0057404	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499640	TGCCTCCTCAGGAGA[A/G]AGGCTGATGCTGTCT	1102
rs765459878	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48506921	ACAGCATCCTTCACT[C/G]ATCTGCCCAACATCA	1102
rs765485960	snp	C/T	1.72686e-05	0.00293837	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502720	TGGACAGTGACCAGC[C/T]TACCCACGGAGAGGA	1102
rs765488210	snp	C/G	1.65004e-05	0.00287227	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512149	GATCCTACCTGCCCA[C/G]AGTTATTATAACCCC	1102
rs765536633	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526640	TAAAAATAGCCTGGG[C/T]GCGGTGGCTCATGCC	1102
rs765565878	in-del	-/TAATC			intron-variant	RCBTB2	GRCh38.p7	13:48525041	ACACTAAGGAGAATT[-/TAATC]TATAGTATTTCCATA	1102
rs765571081	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517589	AGCTAGGATGCACGG[A/G]GCAGCTGTCCCAATG	1102
rs765601225	in-del	-/AAAACCCAG			intron-variant	RCBTB2	GRCh38.p7	13:48531914	TGTCTAGTAAGGTGT[-/AAAACCCAG]CAGGAACGCAATACT	1102
rs765641422	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48496499	CTCTACCCAGGATGG[C/G]AGCCAAGCTGAGCAA	1102
rs765645958	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490214	GTTACTACAGTCAGA[C/T]GGTTTATGCAAAACC	1102
rs765683315	snp	G/T	0.000277701	0.0117802	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533083	TAGCGGTTACTGCAC[G/T]GTCAGGGGCCCGGCG	1102
rs765728226	snp	C/T	3.58661e-05	0.00423459	intron-variant	RCBTB2	GRCh38.p7	13:48496188	GAAGCAAGCTTTCCT[C/T]ACCTGTGCATCATAC	1102
rs765742230	snp	A/C	3.30316e-05	0.00406383	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521951	CCATATGGACTCAGT[A/C]CTGGGCAGTCCCTGA	1102
rs765824262	snp	A/G	1.64846e-05	0.0028709	missense, nc-transcript-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499626	TGGCAATTACCTACT[A/G]CCTCCTCAGGAGAAA	1102
rs765858573	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48491113	TAAAAGTTTCCTCTC[C/T]AAGCTACTGTAGGTA	1102
rs765877141	snp	A/G	3.38266e-05	0.00411244	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496274	TAGTTTGTTGGCAGA[A/G]CTTTTTCAAACGATT	1102
rs765939681	snp	C/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534302	TTGCTCTCAGAAAAA[C/G]CTCACTTCAGTGATG	1102
rs765939727	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48521878	ACACACATGCTCCAA[A/G]GGCATGATTTTTTTC	1102
rs765944821	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490090	AAATGGAAAGGCTCA[A/G]AAACTTTCCTGCAGA	1102
rs765951681	snp	C/G	1.66829e-05	0.00288811	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511775	GTGGACGTACCCTCT[C/G]GACACGGATGCCTTG	1102
rs765971150	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512810	TGACAGATTAGTAGA[A/G]ATATGACAGGGCACT	1102
rs766017668	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48504684	TAACGTGGTGTCTTA[A/C]TGAATATAATCTATG	1102
rs766024783	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48500118	ACGGGTTGAATGATG[C/T]CCTCTAAAAATTCCT	1102
rs766028225	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48522919	CTTATCAATGTTTTC[C/T]ATGCCCTTGAGGATA	1102
rs766065492	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529841	CTGTAACCCCAATAA[C/T]TCCTGGTCTCCAATC	1102
rs766217522	snp	C/T	4.97847e-05	0.00498897	intron-variant	RCBTB2	GRCh38.p7	13:48515368	AATCTATGGGAAAAA[C/T]CACTGTTAGTTCAAG	1102
rs766219907	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48501031	AAGCCAAGCACAAAT[A/G]AATGCATCCTGTATC	1102
rs766230945	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48521525	CTATGATGAATTGAG[-/A]ACATATCATCTAAGA	1102
rs766387904	snp	A/G	3.30251e-05	0.00406343	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521938	GGAAGTTCTTCTTCC[A/G]TATGGACTCAGTCCT	1102
rs766499549	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520033	TTCAGATTAAAGATA[C/T]TCAACTGGTAAGTAT	1102
rs766518932	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490193	TCTGCAAAACCTGAT[A/G]TTTGTGTTACTACAG	1102
rs766581009	snp	C/G	0.00018909	0.00972157	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533066	CCGCTCCGCCTCCTG[C/G]GTAGCGGTTACTGCA	1102
rs766583038	snp	G/T	1.6501e-05	0.00287232	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511875	GTAACCCCAGACATA[G/T]ACCTGAGAGAAAATG	1102
rs766590310	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48496918	CCCACTGCTCCTCTC[C/T]ACAGCAAAACTCCTA	1102
rs766610653	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48506976	ATGTTCCCTTCTGAG[A/T]TGTTTGTTCTTTGTT	1102
rs766693333	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48515115	ATAGTCAATTTCACA[A/G]GAAGAGCTAGCAACT	1102
rs766702215	snp	A/C	1.67933e-05	0.00289765	intron-variant	RCBTB2	GRCh38.p7	13:48512915	AAATAAAAAGAAAGA[A/C]AATCAGTTTTTTACA	1102
rs766779293	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503475	CAGGAGAGCAGTTTC[C/T]TAGGATCACTATGTG	1102
rs766783040	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48516179	AAGAACAACGCTGAA[A/T]GTGACACCAAGGAAA	1102
rs766784428	snp	G/T	1.6507e-05	0.00287284	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502799	TGCAGGAGAAGTGGG[G/T]GAGGTGCGGGAGGAT	1102
rs766802417	in-del	-/CTC	1.70577e-05	0.00292037	cds-indel, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496236	CAGAGCGATGGCATT[-/CTC]CTCGCAGATGCCTTG	1102
rs766855741	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48527022	AAATCCAAAATAGTT[-/A]AAAAAAATGTTTAAT	1102
rs766885513	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514321	TTCATGTCCCAGCTG[A/G]GATGGAGCAAGATGG	1102
rs766925368	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48528339	AGTCCCAGTATTACA[C/T]ATTTTAAAATTCAAC	1102
rs766980058	snp	C/T	4.95692e-05	0.00497816	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502863	CACGTGCCCACCCTG[C/T]GTCTTGGCCGCAGAC	1102
rs767019848	in-del	-/C			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534501	CCTTGCGCACTTGGT[-/C]TTTTACGCATTATGG	1102
rs767037244	snp	C/T	1.64817e-05	0.00287064	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490060	GAAGTGATTCATCTC[C/T]GGCTTTTGCAGGGGA	1102
rs767174027	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48512265	TGGCACCGAGTCTTT[C/G]CTCTCAAAGTGCTTC	1102
rs767177069	snp	C/T	3.31669e-05	0.00407215	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501840	TTCCCTCTTCAGTGA[C/T]TCAGCCACTGTGAGG	1102
rs767253502	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531618	GCGAGCCCAGCAAGA[A/G]CAATAAGGCCTGAGT	1102
rs767312122	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489740	TGGTAAGGACAGACA[A/G]CACTCCTTGTCAAGC	1102
rs767342627	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48501139	CATGAGGGGTCTTTG[A/T]AGGGTGATGGGAATG	1102
rs767389430	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48519025	TCTTCACAACAATTG[C/T]AGGACATAGATATTA	1102
rs767398206	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48521213	ACTTAAGTCTGCACA[C/T]GGTAATGCTACAGTT	1102
rs767536878	snp	A/G	3.29777e-05	0.00406051	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515286	AAGAATCCAGTCTCC[A/G]AGGTTCAATGGTGCT	1102
rs767699782	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529394	TTGTTCAGTATTATA[C/T]ACATACATACACGCA	1102
rs767732503	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499368	CTGCTGCATGGCCCT[C/T]AGTCTCTGTCCCTTC	1102
rs767762559	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48524471	CACACATTTCAGTAA[C/T]GTGACCAATAGTCAC	1102
rs767765195	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48497326	AAATATCATCTATAT[A/G]TGCAGGTGAGTCCTG	1102
rs767778324	snp	A/C	1.65135e-05	0.00287341	stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521930	AGAAAAGAGGAAGTT[A/C]TTCTTCCATATGGAC	1102
rs767839918	snp	A/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534489	AAGATCTGTTTGCCT[A/T]GCGCACTTGGTCTTT	1102
rs767856805	in-del	-/T	1.64838e-05	0.00287083	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515255	AGCTGAGGCAGGCTA[-/T]TTTTTTTGCCATTTA	1102
rs767924966	snp	A/G	3.34857e-05	0.00409167	intron-variant	RCBTB2	GRCh38.p7	13:48512185	AATACCTGTTTAAAG[A/G]AAAGATCAGTAAATG	1102
rs767940463	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509961	AACGTTTTTGCTCTA[C/T]ACTACTATCAGGAAA	1102
rs767946480	in-del	-/C	1.65228e-05	0.00287422	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501798	ATCAACTAGAAACTT[-/C]AGGTCTGCAGTGTCC	1102
rs768003639	snp	A/C	1.72374e-05	0.00293571	intron-variant	RCBTB2	GRCh38.p7	13:48501912	GTTAGCTACAGACAT[A/C]ATGAACACACAGGAC	1102
rs768124829	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512777	AGACCCACAGGCAAC[C/T]TCAATGACTTGTTTG	1102
rs768236690	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48498862	CTACCCAGGCCAAGT[-/A]ACCTCAGTGCAGCCA	1102
rs768254593	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497738	AATAAATCTTATACA[C/T]GTGGTAGACTTTGGT	1102
rs768375179	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534081	CAGACATTTATCTCT[A/G]TTCTCTGAGCATAGC	1102
rs768476140	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48521214	CTTAAGTCTGCACAC[A/G]GTAATGCTACAGTTT	1102
rs768509742	snp	A/C	0.000132974	0.00815288	intron-variant	RCBTB2	GRCh38.p7	13:48511992	AACACGGTTTTTAAA[A/C]AAGATGTAAAATAAC	1102
rs768510734	snp	C/T			intron-variant, missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504385	AGTCAATTTTGTCCA[C/T]ACACCCTGTTTCAAC	1102
rs768516566	snp	G/T	1.64784e-05	0.00287035	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512111	TGACTCTTCGAGGGA[G/T]TGGCTGATTAACTGT	1102
rs768630812	snp	C/T	3.29826e-05	0.00406082	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512875	TATAAGCATTATGAC[C/T]CCAGGTAAAGACTTC	1102
rs768707298	snp	G/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503036	AAGGGTCAGGAAAAG[G/T]AAAAAACAAAACAAA	1102
rs768730049	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514200	AATAAGGGTGACTTG[A/G]ACACAAGCACTATGA	1102
rs768758613	snp	C/T			missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501785	AAATGTACTTTCCAT[C/T]AACTAGAAACTTCAG	1102
rs768827720	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48516897	AACAGCCAATATGTC[-/T]TATCAAATGGCATGT	1102
rs768833419	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506779	AAGCATTTATGAACT[A/G]CTCTTCCTTTCTTCA	1102
rs768853886	snp	C/G	4.9826e-05	0.00499104	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515726	TCTTCAAAGATGACA[C/G]AGTAGCCTGTACTGG	1102
rs768862908	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48511572	TATTCCAAAAGGTAT[A/G]TGACAGTGCCCTGGA	1102
rs768897121	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531378	TCATACCCTTACAAA[C/T]ATATAATATCAGATG	1102
rs768904924	snp	G/T	3.37325e-05	0.00410672	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496261	ATGCCTTGCTTGATA[G/T]TTTGTTGGCAGAGCT	1102
rs769066607	snp	C/T	1.67823e-05	0.0028967	intron-variant	RCBTB2	GRCh38.p7	13:48515176	AGCTGCGAATAAAGC[C/T]GAAATTCTACATGGG	1102
rs769076994	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48519599	TTTTATGAAATGATG[C/T]TACAAGTCAAGAGAA	1102
rs769090193	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507401	GCGACAGACAATGAC[C/T]ATCAACTGAGCTAAC	1102
rs769160623	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48495146	AAAAGGAAACTGACT[C/T]GAAGATGTTACAGCC	1102
rs769205026	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505185	TAGCACCTAGGAGCC[C/T]TGGTTTCATCACATT	1102
rs769228635	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48515956	GATGGAACCAGGTCT[A/C]CCCTACTCATTGTCC	1102
rs769273128	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532178	TTCATTCTAAATTAG[C/G]CTTCCAACTCAGTTC	1102
rs769320682	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516985	CTAAGGCCTCTCTTT[C/T]CCATCAGTTATTAAA	1102
rs769377680	snp	A/G	1.66335e-05	0.00288383	intron-variant	RCBTB2	GRCh38.p7	13:48511969	ACTGGCATGAGACTG[A/G]TGTGGCAAACACGGT	1102
rs769432633	snp	A/G	6.61255e-05	0.00574964	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501805	AGAAACTTCAGGTCT[A/G]CAGTGTCCGGGTTGT	1102
rs769526234	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48523790	ACCGATCCTGGGCTT[C/T]TGAGTAGGAAATAAC	1102
rs769548359	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498966	TAGAATCTGATCTCT[C/T]TTCAATACTTCCACT	1102
rs769593070	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48522476	TGGCTTTGTTATTCT[A/G]GACTTAATGAAAAAT	1102
rs769605835	snp	C/G/T	4.94208e-05	0.00497075	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490131	TTTTAAAGGCTCCAA[C/G/T]TCTGCTTGCTTTGCT	1102
rs769627131	snp	A/G	5.12921e-05	0.00506393	intron-variant	RCBTB2	GRCh38.p7	13:48501901	ATGCTTCCAGAGTTA[A/G]CTACAGACATAATGA	1102
rs769661503	snp	A/G	0.000579206	0.0170079	intron-variant	RCBTB2	GRCh38.p7	13:48522408	GATTTGCTAAGCTGG[A/G]AAAAAAAAAGGAGAA	1102
rs769741182	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48505284	TGGTTGCATGACAAT[A/G]GAGGTTTCTTTACAT	1102
rs769759923	snp	C/T	1.65151e-05	0.00287355	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521912	CCTTGCCACTGTCTC[C/T]AGAGAAAAGAGGAAG	1102
rs769784196	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534256	ACTGGTTACATCTTA[C/T]CAATGAAAGAAATTT	1102
rs769826430	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48490847	GCTTTAAAGAAATCA[A/T]GACTTCCAAGTCTCT	1102
rs769831025	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48492015	CTTCATGTTCAAAAT[A/G]GGGCCCTCTGTTCTG	1102
rs769853603	snp	A/G	4.9918e-05	0.00499565	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502756	CACGTGACGGCGGGC[A/G]TGGCAAAGCAGGCAA	1102
rs769890118	snp	A/G	8.24165e-05	0.00641883	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511851	GAGTCCAAGCTGCCC[A/G]TTTCCGTTGTAACCC	1102
rs769890655	snp	C/G	3.38203e-05	0.00411206	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496249	TTCTCCTCGCAGATG[C/G]CTTGCTTGATAGTTT	1102
rs769966236	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48519728	ATAACCTAAGTACAA[A/C]AGAGATGTGAATACA	1102
rs770159466	snp	C/T	1.65217e-05	0.00287412	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515621	ATAAAACTTCATTGC[C/T]AGCACTGCCAAAGAC	1102
rs770183995	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48528196	TTCTGTCCACATTAC[C/G]CCAACCCAATGGTAG	1102
rs770267136	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491189	ATGAACATTACACAC[A/G]ATAGTCTTTTCTTCT	1102
rs770271348	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48522618	AGCAGAAGCTATGCA[A/G]TATGTCTGGACTGTG	1102
rs770284986	in-del	-/AG			intron-variant	RCBTB2	GRCh38.p7	13:48516099	AAGCAAGAGAGACAG[-/AG]AGAGAGAGAGAGAGA	1102
rs770316057	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497934	CAAGCCCCAGCTCTG[C/T]GCCTCCTCCACGCAC	1102
rs770351905	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528507	ACAGGAAATTAAATA[A/G]TATCGATATCTTTTA	1102
rs770359534	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518008	CACAGGGACTGCAGT[A/T]ATGCATCTGGAAGTC	1102
rs770371835	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505465	TGCTGTGCAAAAGAA[C/T]CGTGCCAGACGGGGA	1102
rs770380355	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48492347	CTCTACCAACTGTCC[C/T]CTGCATCACTGGCTT	1102
rs770420502	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48507495	AAAAATCACTACATG[C/T]TGATAATAAACAGGT	1102
rs770431194	snp	A/C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498514	GATGGGCGGATCACC[A/C/T]GAGGTCGGGAGTTCA	1102
rs770435872	in-del	-/C	1.6476e-05	0.00287014	frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512765	CAAAGAATGGTAAGA[-/C]CCACAGGCAACTTCA	1102
rs770449458	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506574	TCTAAGAAAACCCCC[A/G]GCTGGCAGTGCTGAG	1102
rs770582036	snp	A/C	1.64836e-05	0.0028708	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511837	TTGCCACTGTTGCCG[A/C]GTCCAAGCTGCCCGT	1102
rs770656691	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48513654	ATTGATAATCATATT[C/G]TTCATTTGGATCTTT	1102
rs770707968	snp	A/G	1.64803e-05	0.00287052	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512861	ATTGCCCAGCTGGCT[A/G]TAAGCATTATGACCC	1102
rs770775435	in-del	-/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503473	CCCAGGAGAGCAGTT[-/T]CCTAGGATCACTATG	1102
rs770788152	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526246	ATCTGTAAAATAAAA[C/T]TGAATCAATACCCTA	1102
rs770803040	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48526219	AACTCATAAACTATA[A/G]TTTCTTTAGCCATCT	1102
rs770961013	snp	C/G			utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48522341	GGGATTGGAAAGTTC[C/G]AAATCACGGGGAAGA	1102
rs770982408	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48524055	CAAGATTAATTACTA[C/T]TGTATAATACTATTA	1102
rs771026288	snp	A/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489253	TAAGAGACCTATTTT[A/T]TAGTGAGTGACATGA	1102
rs771090338	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508549	ACTGGGATTACAGGC[A/G]TGTGCCACTGTGCCC	1102
rs771090626	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510651	TTTCCACAGTGACAG[A/G]AGTAGGATAGGACTG	1102
rs771142023	snp	C/T	7.20565e-05	0.00600192	intron-variant	RCBTB2	GRCh38.p7	13:48496171	CAGGAGGCCGGCAGC[C/T]GGAAGCAAGCTTTCC	1102
rs771150760	snp	G/T			utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533064	GTCCGCTCCGCCTCC[G/T]GGGTAGCGGTTACTG	1102
rs771163319	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48529306	TTGTTAAAGATCTTT[A/G]ACCCACAGCATATAT	1102
rs771175640	snp	A/T	1.65176e-05	0.00287376	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501784	TAAATGTACTTTCCA[A/T]CAACTAGAAACTTCA	1102
rs771177508	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518956	AAGTGGAACAAGTAT[A/T]TAATGTAGATGTTAA	1102
rs771244083	snp	A/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503946	TGAAGGAAAATGGTA[A/T]ACTCTTTTAACCCAG	1102
rs771326796	snp	A/C/T	4.9626e-05	0.00498106	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515208	TTCCTAGGTTACCTG[A/C/T]TGTTGCAAGGACAAT	1102
rs771334128	snp	C/T	1.69896e-05	0.00291454	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496241	CGATGGCATTCTCCT[C/T]GCAGATGCCTTGCTT	1102
rs771362572	snp	C/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499315	CACAGTCTGAAATAA[C/G]TGGAATTCCTGGGCC	1102
rs771378802	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48530152	ACATTTGACTGCCTT[A/G]GTCTCCCCCAAAGCG	1102
rs771471964	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48495354	TAGATAATGAATTTT[A/G]GTTTTTTATTCAGCT	1102
rs771510230	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48494206	TTAGAATAATCCCTG[A/G]CTCATATTAATTATG	1102
rs771577980	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48523553	AACTGGCCTGTAACC[-/A]AAGTTCCCTCTCCTT	1102
rs771608200	snp	C/T	4.11862e-05	0.00453777	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502951	ACATAAGCACAGTGA[C/T]CGGGGCAGAAACAAG	1102
rs771713864	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48498375	TTAGACATATGGAAC[A/G]TAGGTCTCCATTTGG	1102
rs771740563	snp	A/G	1.66399e-05	0.00288438	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515730	CAAAGATGACAGAGT[A/G]GCCTGTACTGGCTGA	1102
rs771746687	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506721	ATCTGGCATTCTCTG[A/G]GAGCAGGGGAGGTTA	1102
rs771797796	snp	C/T	5.0822e-05	0.00504068	intron-variant	RCBTB2	GRCh38.p7	13:48511765	CAAACTGACAGTGGA[C/T]GTACCCTCTGGACAC	1102
rs771816977	snp	C/T	1.64814e-05	0.00287061	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512126	TTGGCTGATTAACTG[C/T]TGATCCAGATCCTAC	1102
rs771898594	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48532311	TTTCTTCCCATCCCT[C/T]CGCAGTTCCAAAACG	1102
rs771922662	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514736	GAGAAGTTTTATTTA[C/T]TTTCTTCCTTTTTTC	1102
rs771974782	snp	C/T	1.68021e-05	0.0028984	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502751	GGCGCCACGTGACGG[C/T]GGGCGTGGCAAAGCA	1102
rs771996300	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48508369	GAAATTCAAGTACGG[-/A]AAACAGAAAATCAGG	1102
rs772014620	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502981	GTTGGGTCCTCCTCC[C/T]GCCAGGTTTAACTGA	1102
rs772067159	in-del	-/CACTCT			intron-variant	RCBTB2	GRCh38.p7	13:48499141	ACACACACACACACA[-/CACTCT]CTCTCTCTCTCTCTC	1102
rs772212720	snp	C/T	0.00011544	0.00759649	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499742	GTTATCTTCCAATGA[C/T]GAACGAAAATGCTCA	1102
rs772237548	snp	G/T	1.66649e-05	0.00288655	intron-variant	RCBTB2	GRCh38.p7	13:48515191	TGAAATTCTACATGG[G/T]GTTCCTAGGTTACCT	1102
rs772268610	snp	A/G			utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48522357	AAATCACGGGGAAGA[A/G]CGGACATCAATTCTC	1102
rs772281414	snp	C/G			intron-variant, stop-gained, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517306	TTTGTGTTGGTTAAT[C/G]AACAAGTAAATGAAT	1102
rs772373184	snp	A/T	1.6552e-05	0.00287676	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499578	AACCACCTTGTCAGT[A/T]CCTCAACATTTTGCC	1102
rs772404353	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48491617	GCATCATCTCTTTGG[C/G]TGAAGTCTACAGAGA	1102
rs772419808	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48516465	GCTGTGAGGGAAGGA[A/T]CTCTTCCAGGCTGTG	1102
rs772435640	snp	A/G	6.59174e-05	0.00574059	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499727	TACAATATCATCCTC[A/G]TTATCTTCCAATGAC	1102
rs772491352	snp	C/T	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510645	TGTCCTTTTCCACAG[C/T]GACAGGAGTAGGATA	1102
rs772522276	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48531247	TTTTGTTGAATAAAT[C/G]AATGAATCTAGGTTG	1102
rs772535128	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48518192	TCATTTGTTACAGCA[A/G]CACAAAGAAACTAAC	1102
rs772560311	in-del	-/T	1.66062e-05	0.00288146	intron-variant	RCBTB2	GRCh38.p7	13:48511999	TTTTTAAACAAGATG[-/T]AAAATAACTTCCTTA	1102
rs772646873	in-del	-/AAGT			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489997	TCTTCTGACAGTTAC[-/AAGT]AAGTACTCAGCCAAA	1102
rs772712475	in-del	-/CA			intron-variant	RCBTB2	GRCh38.p7	13:48493225	CTAAGTACCCTCCTT[-/CA]CACACACACACACAC	1102
rs772720094	snp	A/G	5.06453e-05	0.00503191	intron-variant	RCBTB2	GRCh38.p7	13:48511766	AAACTGACAGTGGAC[A/G]TACCCTCTGGACACG	1102
rs772734744	in-del	-/TCTCTCTTCTT/TCTCTTCTT			intron-variant	RCBTB2	GRCh38.p7	13:48493345	TCTCTCTCTCTTCTC[-/TCTCTCTTCTT/TCTCTTCTT]TTCTCTCTCTCACCC	1102
rs772746174	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48525625	AACAAGTCCTGCAAT[C/T]TTAGCAACACTGCCC	1102
rs772755191	snp	A/G	6.67011e-05	0.00577461	intron-variant	RCBTB2	GRCh38.p7	13:48512904	TCTCCTTCTGAAAAT[A/G]AAAAGAAAGACAATC	1102
rs772775125	snp	C/G	1.65288e-05	0.00287474	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499596	TCAACATTTTGCCAA[C/G]TTTTTGGAAGTCTTT	1102
rs772794895	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48515058	TGCCACATCACCTTA[C/T]GCTGGCATTCAGATA	1102
rs772829185	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48495383	TATTTATACTTTTTC[-/A]AAAAAATAAAAATAG	1102
rs772923098	snp	A/C	1.67607e-05	0.00289483	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515738	ACAGAGTAGCCTGTA[A/C]TGGCTGAAAAGGAAA	1102
rs772969437	in-del	-/G	6.59109e-05	0.0057403	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490084	CAGGGGAAATGGAAA[-/G]GCTCAAAAACTTTCC	1102
rs773048320	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48522589	CAGGTAAAAGTAACA[C/G]CAGGAGCAGCTCTAG	1102
rs773053448	snp	A/C	1.66438e-05	0.00288472	intron-variant	RCBTB2	GRCh38.p7	13:48512698	AATCTTATTGAAAAA[A/C]ATCAATGAGCTTTAT	1102
rs773053565	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48499897	TCTTTGCTGGCCAGG[G/T]TTTTCAAACAATCAT	1102
rs773104852	snp	A/C/T	6.69595e-05	0.00578583	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502755	CCACGTGACGGCGGG[A/C/T]GTGGCAAAGCAGGCA	1102
rs773116089	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489078	AGATACACATTAGAA[A/G]AATCTGAGACTATGT	1102
rs773138398	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519816	TTTTTAAGTTTGTTA[A/G]GGCAACTATTACATA	1102
rs773217620	snp	G/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534270	ATCAATGAAAGAAAT[G/T]TATGAGTTAAACAGG	1102
rs773331141	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48532242	TCAATGTCTGAAAAC[C/T]TCTATTTCCAGGGCT	1102
rs773375051	snp	A/C	1.65135e-05	0.00287341	stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521933	AAAGAGGAAGTTCTT[A/C]TTCCATATGGACTCA	1102
rs773401218	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48520882	CTCAACTTTTGAGTA[C/G]TTCCTAGCATTATAA	1102
rs773419369	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531550	GTGGGAAAGTGAGCA[C/T]TGAGCATACTGGAAA	1102
rs773456427	snp	C/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490140	CTCCAACTCTGCTTG[C/G]TTTGCTGATAAAGTT	1102
rs773484003	snp	A/T	1.99591e-05	0.00315898	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502936	TCACAAACACACACC[A/T]CATAAGCACAGTGAC	1102
rs773484051	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507668	AATATTGGAGAAGAA[A/G]CAGCAAAGATGACAG	1102
rs773563239	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528263	TTCTAAATGCTAATA[A/G]TTCTTCTTTAGAAGT	1102
rs773567696	snp	C/T			missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502778	AGCAGGCAAACACGT[C/T]GTCAGTGCAGGAGAA	1102
rs773582061	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529571	CGTAAAAGAAACCCA[C/T]TCTAATGTCAAATTA	1102
rs773815438	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48517177	CCTCATTACCATGAA[A/T]TTCTCTGGGGCCACC	1102
rs773819158	in-del	-/CTCT/CTCTCTCT/CTCTCTCTCTCT			intron-variant	RCBTB2	GRCh38.p7	13:48493311	ACACACACACACACA[-/CTCT/CTCTCTCT/CTCTCTCTCTCT]CACACTCTCTCTCTC	1102
rs773828865	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48492375	CTTGTTCCCCTTCAC[C/T]GAGTCATTTGCATCA	1102
rs773858097	snp	C/T	1.66452e-05	0.00288484	intron-variant	RCBTB2	GRCh38.p7	13:48515194	AATTCTACATGGGGT[C/T]CCTAGGTTACCTGTT	1102
rs773862078	snp	C/T	1.65154e-05	0.00287358	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502860	GTACACGTGCCCACC[C/T]TGCGTCTTGGCCGCA	1102
rs773916506	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48493961	TTGTTGAATCCATGC[A/G]TAAATACTCCTGATT	1102
rs773979551	snp	A/C	3.30104e-05	0.00406252	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515316	TCTGGACGTCACCTA[A/C]CCCCAAACAGCCACA	1102
rs773997365	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48501045	TGAATGCATCCTGTA[A/T]CATCCCATCTAAATA	1102
rs774022418	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505494	GAAAATGGTTAACAA[C/T]ATTTGGCTTCTCAAT	1102
rs774081234	snp	A/G	1.6609e-05	0.0028817	intron-variant	RCBTB2	GRCh38.p7	13:48511995	ACGGTTTTTAAACAA[A/G]ATGTAAAATAACTTC	1102
rs774134515	snp	C/G	6.62526e-05	0.00575516	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501831	GTTGTCAAATTCCCT[C/G]TTCAGTGACTCAGCC	1102
rs774176647	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48513719	AGCTCATTTTAATTT[A/C]TTCAAATAATAAATA	1102
rs774270320	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48501902	TGCTTCCAGAGTTAG[C/G]TACAGACATAATGAA	1102
rs774376810	snp	C/T	5.23729e-05	0.005117	intron-variant	RCBTB2	GRCh38.p7	13:48501918	TACAGACATAATGAA[C/T]ACACAGGACAGGATA	1102
rs774416535	in-del	-/GATTT			intron-variant	RCBTB2	GRCh38.p7	13:48511357	TAATCATTAACTTAC[-/GATTT]GATTAGTAAATTCTG	1102
rs774502207	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48520189	GCAATATACATTCTT[A/C]TGTCCAGCACACTCA	1102
rs774570947	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530166	TGGTCTCCCCCAAAG[C/T]GCTGGGATTACAGGT	1102
rs774575988	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48520991	CATTATAACACTTTG[C/T]ATATATATTTGTATA	1102
rs774630425	snp	C/T	1.6492e-05	0.00287154	stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512876	ATAAGCATTATGACC[C/T]CAGGTAAAGACTTCT	1102
rs774702824	in-del	-/AG			frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512806	GTTTGACAGATTAGT[-/AG]AGAGATATGACAGGG	1102
rs774755710	snp	A/T	5.20747e-05	0.00510242	intron-variant	RCBTB2	GRCh38.p7	13:48511755	TACACGCACACAAAC[A/T]GACAGTGGACGTACC	1102
rs774756001	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48504719	ACTTTACTGACTGAG[A/G]AAGACTCAACAACAC	1102
rs774810721	snp	C/G	1.81076e-05	0.0030089	intron-variant	RCBTB2	GRCh38.p7	13:48496365	AGTGATTTCAAGCAT[C/G]CTGATTTACAGTTGC	1102
rs774866433	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48502041	CATCTCTGTAATCAT[C/T]AAGAATAAGAATCTC	1102
rs774925743	snp	C/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499489	AACAAGGGAAACGTG[C/T]TTGGATTCAACACAC	1102
rs774948613	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48529376	TTCCACTTGAGATTG[A/G]TTTTGTTCAGTATTA	1102
rs774971904	in-del	-/CAGT			intron-variant	RCBTB2	GRCh38.p7	13:48530648	TTCACTAGTCATCCA[-/CAGT]CAGAGGGACATTTAG	1102
rs775002328	snp	C/G	1.64757e-05	0.00287012	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512773	GGTAAGACCCACAGG[C/G]AACTTCAATGACTTG	1102
rs775078725	snp	A/G	1.65135e-05	0.00287341	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515215	GTTACCTGTTGTTGC[A/G]AGGACAATATGTGGA	1102
rs775082268	snp	A/G	1.65367e-05	0.00287543	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501810	CTTCAGGTCTGCAGT[A/G]TCCGGGTTGTCAAAT	1102
rs775125757	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48494253	AGCATGAGGGATAAT[A/T]ATTTGCTGAAAGAGC	1102
rs775131688	snp	G/T	3.29919e-05	0.00406138	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515303	GGTTCAATGGTGCTC[G/T]GGACGTCACCTAACC	1102
rs775190332	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48529336	TATTCCTTCAACATG[C/G]CAGGCCCTCTTGGCC	1102
rs775264377	snp	C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511855	CCAAGCTGCCCGTTT[C/T]CGTTGTAACCCCAGA	1102
rs775275059	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48520844	ATACCTAGCAAAAAA[C/G]AGTTAAGAAAAAATG	1102
rs775291454	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48519286	ATACCTACTGTGGGT[C/T]GTCTTCCACAAACAG	1102
rs775315314	snp	G/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502629	AGAAATAAATTATGA[G/T]AGTGCACCTAACAAA	1102
rs775399649	snp	A/G			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503024	TAAAATTACAAAAAG[A/G]GTCAGGAAAAGGAAA	1102
rs775468695	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508712	CCATCCATGATTTTT[A/G]TAACCAAATTATAAT	1102
rs775478271	snp	A/G	0.000186376	0.00965159	intron-variant	RCBTB2	GRCh38.p7	13:48532987	CCACGTCACGGCCGC[A/G]ATCCCCCTCGGCCTC	1102
rs775495256	snp	C/T	1.65201e-05	0.00287398	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512156	CCTGCCCAGAGTTAT[C/T]ATAACCCCAGGCAAA	1102
rs775527475	snp	A/G	1.66308e-05	0.00288359	intron-variant	RCBTB2	GRCh38.p7	13:48511976	TGAGACTGATGTGGC[A/G]AACACGGTTTTTAAA	1102
rs775599819	snp	C/T	1.66338e-05	0.00288386	intron-variant	RCBTB2	GRCh38.p7	13:48499789	GCAGTATGTCAGGTC[C/T]TAGCTTCCCAGCCAG	1102
rs775599872	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48502152	CATTTGAGTAAATAC[A/G]CTAGTTAAAAGTAAA	1102
rs775599908	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514780	TCAGAGCAAGGAATT[C/T]TTCTAGTCAATCCCT	1102
rs775629241	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48522407	TGATTTGCTAAGCTG[C/G]AAAAAAAAAAGGAGA	1102
rs775687127	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518258	CACCCTGTGAGTTAA[C/T]GGCAGAGCCTGTACC	1102
rs775709323	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48500863	CAGGTTGATGTGATA[C/T]AGAGAGAGTGAGCAA	1102
rs775716581	in-del	-/ATG			intron-variant	RCBTB2	GRCh38.p7	13:48509520	CTACAAGATGTGTGA[-/ATG]ATGAACAGCTGCAGG	1102
rs775717178	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48510398	ACTGCAGTTTGCTTA[C/G]AATAGCTGTTGGAGG	1102
rs775772916	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48506742	GGGGAGGTTAGGGCA[G/T]CCCAATGAACAATGT	1102
rs775801130	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48513680	TCTTTTCAAATCTTC[C/T]ATAATCCCTGCAGAT	1102
rs775883498	snp	C/G/T	3.37338e-05	0.00410682	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496259	AGATGCCTTGCTTGA[C/G/T]AGTTTGTTGGCAGAG	1102
rs776027548	in-del	-/A	1.65754e-05	0.00287879	intron-variant	RCBTB2	GRCh38.p7	13:48515362	ACAAAAATCTATGGG[-/A]AAAAACCACTGTTAG	1102
rs776030242	snp	C/G	7.16486e-05	0.00598491	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496191	GCAAGCTTTCCTTAC[C/G]TGTGCATCATACTTC	1102
rs776065262	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48515924	GCGGCTCACAGCCAT[C/T]GAGCAGCGGAGGCCC	1102
rs776070208	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530330	CATAAGCAAATTCCA[C/T]GGACTCCTTACATTT	1102
rs776083243	snp	A/T			intron-variant, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517310	TGTTGGTTAATGAAC[A/T]AGTAAATGAATGGCT	1102
rs776161825	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531277	GAGTTCAGTAAAAAA[A/G]TATCTCTGGAGTAAG	1102
rs776173398	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514941	CAAGAATCCAAAGTT[C/T]AGACAGACTTGCCAA	1102
rs776265220	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499628	GCAATTACCTACTGC[C/T]TCCTCAGGAGAAAGG	1102
rs776336119	snp	A/G/T	3.29659e-05	0.00405981	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511838	TGCCACTGTTGCCGA[A/G/T]TCCAAGCTGCCCGTT	1102
rs776364813	snp	A/G	1.6517e-05	0.00287372	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501787	ATGTACTTTCCATCA[A/G]CTAGAAACTTCAGGT	1102
rs776367175	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48528184	TCTCTTAGGGACTTC[G/T]GTCCACATTACCCCA	1102
rs776439243	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48504408	GTTTCAACAAACAGG[A/C]TTTCTCATTGACCTT	1102
rs776479478	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533383	CCAGGGTTATGTTCT[C/T]GCAAATTTTGGGAAT	1102
rs776480028	snp	C/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534212	GCGATAGTGCAGAGA[C/G]GCATCGTGTGCCTGC	1102
rs776569385	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48531386	TTACAAATATATAAT[A/T]TCAGATGGTGATTAA	1102
rs776612452	snp	C/T	0.00019006	0.00974648	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533075	CTCCTGGGTAGCGGT[C/T]ACTGCACGGTCAGGG	1102
rs776626075	in-del	-/ACTC			intron-variant	RCBTB2	GRCh38.p7	13:48499142	CACACACACACACAC[-/ACTC]TCTCTCTCTCTCTCT	1102
rs776644289	snp	C/T	3.30792e-05	0.00406675	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501813	CAGGTCTGCAGTGTC[C/T]GGGTTGTCAAATTCC	1102
rs776710662	snp	C/G			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489746	GGACAGACAGCACTC[C/G]TTGTCAAGCTATCTA	1102
rs776717208	snp	C/T	0.000116557	0.00763314	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511778	GACGTACCCTCTGGA[C/T]ACGGATGCCTTGCAA	1102
rs776718942	snp	C/T	1.65168e-05	0.00287369	intron-variant	RCBTB2	GRCh38.p7	13:48521891	AAGGGCATGATTTTT[C/T]TCTAACCTTGCCACT	1102
rs776794827	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48499896	TTCTTTGCTGGCCAG[G/T]GTTTTCAAACAATCA	1102
rs776847207	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48501023	AAAGAAAGAAGCCAA[C/G]CACAAATGAATGCAT	1102
rs776906303	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508555	ATTACAGGCATGTGC[C/T]ACTGTGCCCAGCTAA	1102
rs776922510	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533376	ACCTTCTCCAGGGTT[A/G]TGTTCTCGCAAATTT	1102
rs776931837	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48491034	GGTGCTGAGACCTCC[A/T]ATATGCCTCAAACCC	1102
rs776960986	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530430	AGGGGAAACACACTT[C/T]ACTTTCTAAAATTAT	1102
rs776975316	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48500560	AAGACTCTGCCATCT[-/A]AAAAAAATAAGGTGG	1102
rs776976794	snp	A/G	0.000379266	0.0137655	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515296	TCTCCGAGGTTCAAT[A/G]GTGCTCTGGACGTCA	1102
rs777039733	snp	A/G	1.64735e-05	0.00286993	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510653	TCCACAGTGACAGGA[A/G]TAGGATAGGACTGGT	1102
rs777175388	in-del	-/ACA			intron-variant	RCBTB2	GRCh38.p7	13:48519015	TTATTTCTGATCTTC[-/ACA]ACAATTGTAGGACAT	1102
rs777310290	snp	A/T	1.64781e-05	0.00287033	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490202	CCTGATGTTTGTGTT[A/T]CTACAGTCAGATGGT	1102
rs777310431	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519631	GTGGGATCTGATAGT[A/G]TCATTGACTAAGGTA	1102
rs777312145	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506812	TTTTAGCACTTTGCA[A/G]TGACCTACTAGGCAA	1102
rs777335987	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48530501	TGGATTGAAATTTAG[A/T]TAGGTCTATCTGGTT	1102
rs777381094	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507193	GAAGTCAGGGGTGGG[A/G]CGCGGATTTGGTTGG	1102
rs777422076	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48528197	TCTGTCCACATTACC[C/G]CAACCCAATGGTAGG	1102
rs777468587	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48495614	TCCTTGAAGAATTAT[A/G]TCTTTAATTTAAGGT	1102
rs777515977	snp	C/T	6.59348e-05	0.00574135	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511835	GGTTGCCACTGTTGC[C/T]GAGTCCAAGCTGCCC	1102
rs777582975	in-del	-/CA			intron-variant	RCBTB2	GRCh38.p7	13:48493227	AAGTACCCTCCTTCA[-/CA]CACACACACACACAC	1102
rs777585618	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48493616	TGCTCCCTCCACACC[A/G]GGCTTGCTTTTCCCA	1102
rs777596415	snp	A/T	1.65214e-05	0.0028741	intron-variant	RCBTB2	GRCh38.p7	13:48521976	CCCTGAGGAAAAAGT[A/T]TGTGGTAAAATCAGG	1102
rs777707173	snp	A/C	1.75234e-05	0.00295997	intron-variant	RCBTB2	GRCh38.p7	13:48512947	CATCTACTTCATTAT[A/C]CGAAAATATATGTAG	1102
rs777781904	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506537	GGGAGGGAGAGGAGC[A/G]GAAGGTGGCCCAGGG	1102
rs777794080	snp	A/C/G	1.65296e-05	0.00287481	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515339	CAGCCACAGCAGTTT[A/C/G]TGCCAAGCACAAAAA	1102
rs777824108	snp	C/G	1.67253e-05	0.00289178	intron-variant	RCBTB2	GRCh38.p7	13:48515395	CAAGCAGTTCTATTT[C/G]TAACAAATCTATAAA	1102
rs777937265	in-del	-/ATATATATATATAT			intron-variant	RCBTB2	GRCh38.p7	13:48525374	AGCAAAGGATTCATG[-/ATATATATATATAT]ATATATATATATATA	1102
rs777945661	snp	A/G	1.65408e-05	0.00287578	intron-variant	RCBTB2	GRCh38.p7	13:48511908	ACCCTCAATCCTCTC[A/G]AGAGACAAATGGCCA	1102
rs778141986	snp	A/G	1.65195e-05	0.00287393	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501776	TATGTGCATAAATGT[A/G]CTTTCCATCAACTAG	1102
rs778167782	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510723	CGCCCCAAGCATACA[C/T]TTGGCCTTCATCTGT	1102
rs778175279	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48523471	TATAACCCACAGCCC[A/G]TGGCTCAGAGTAAAA	1102
rs778257872	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509666	TTAACCTATGTTAAA[C/T]TGGTTAAATAAAACT	1102
rs778267103	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48510882	AAGAGGCAGCCTACC[C/T]GTAGGAGAGGCAAGC	1102
rs778339868	snp	A/G	4.94279e-05	0.00497107	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512820	GTAGAGATATGACAG[A/G]GCACTAAACCATGAT	1102
rs778347666	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498974	GATCTCTTTTCAATA[C/T]TTCCACTGCTATACA	1102
rs778372426	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48506682	AAGGGCCTTCTGTGT[G/T]TGAACCACCTCAATT	1102
rs778459051	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531995	GTCTGGGGGAAAGAG[C/T]AACGATCCAGAGCAC	1102
rs778462314	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507251	TGCAGAAAGTTTAGA[A/G]GGTACTTTCAGGTCT	1102
rs778565965	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531152	TGCTAGAATGTAAGC[C/T]CCAGAGGGAAGGGAT	1102
rs778631417	snp	A/G/T	0.00612786	0.0550139	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515728	TTCAAAGATGACAGA[A/G/T]TAGCCTGTACTGGCT	1102
rs778636389	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497477	CAGCATCTGAAAGAT[C/T]CTATTTGTTTTTCTG	1102
rs778655504	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518129	TTGATTTCAGACTTC[C/T]AGCCTCCAGAACTGT	1102
rs778719847	in-del	-/CT					GRCh38.p7	13:48493279	TCTCTCTCTCACCCT[-/CT]CTCTCTCTCCACACA	1102
rs778749257	snp	A/G	1.6684e-05	0.00288821			GRCh38.p7	13:48512684	ATAGAAGTCTACATA[A/G]TCTTATTGAAAAAAA	1102
rs778787064	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496236	CAGAGCGATGGCATT[C/T]TCCTCGCAGATGCCT	1102
rs778815765	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48527881	CATTCATTCTTAATC[A/C]TCACATAAAGTCAAA	1102
rs778832377	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508023	TTTAAAAGGTTTCCC[C/T]TGGATGGTTGCTCCA	1102
rs778901959	snp	G/T	1.65321e-05	0.00287502	missense, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501752	CTTACCGAATCTTGA[G/T]AAGGACTTTATGTGC	1102
rs778907410	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514609	TAACTTCTATCATGC[C/T]CTTAAGGCACTTGCC	1102
rs778907490	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48528588	ACATAAATTTCAATA[G/T]GATAATGATGGTTCC	1102
rs778912660	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48493004	TGCTCCTATCTTCTA[C/T]ATCTCAATAGATGCC	1102
rs778983293	snp	C/T	1.73339e-05	0.00294392	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496304	TTTCTCTATAAAATG[C/T]AGCCAAGTCTAGCAG	1102
rs779026247	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48508248	TCCCTGGAAAGGGTG[G/T]AGAAGTGCAGAACAA	1102
rs779035573	snp	C/T	3.43354e-05	0.00414325	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502907	GACAGGCTGCAATCT[C/T]GATAATCCTAAATTC	1102
rs779053097	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48519839	ATTACATAGGGAACT[G/T]ATGACTAAATTTATA	1102
rs779126948	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534058	AACTGCCTTTCTGCT[A/G]CATAGGGCAGACATT	1102
rs779246728	snp	A/T	1.6764e-05	0.00289512	intron-variant	RCBTB2	GRCh38.p7	13:48515179	TGCGAATAAAGCTGA[A/T]ATTCTACATGGGGTT	1102
rs779287890	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48504949	ATCGTTCTTAGCCCT[C/T]GAAAACCACCCAAAA	1102
rs779364315	snp	G/T	1.64882e-05	0.00287121	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511822	CAAGGGGTTGGCTGG[G/T]TGCCACTGTTGCCGA	1102
rs779372282	snp	C/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501543	CTAAGGAACGCCTAT[C/G]GTACTGGTTCCCGGA	1102
rs779373072	snp	A/G	3.2956e-05	0.00405918	stop-gained, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512105	AGCCAGTGACTCTTC[A/G]AGGGATTGGCTGATT	1102
rs779419368	snp	C/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499711	AAAATTCACTCATTT[C/G]TACAATATCATCCTC	1102
rs779421298	snp	A/G	3.30387e-05	0.00406427	intron-variant	RCBTB2	GRCh38.p7	13:48511892	CCTGAGAGAAAATGA[A/G]ACCCTCAATCCTCTC	1102
rs779582767	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48497558	TGTCATTGCTGAAAT[A/G]AGTGGTAGCCAGGAT	1102
rs779726071	in-del	-/CT			intron-variant	RCBTB2	GRCh38.p7	13:48498722	GCAACAAGAGTGAAA[-/CT]CTGTCTCAAAAAAAA	1102
rs779758040	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507288	GTGACCCAAGCAACC[A/G]CTAAGGAATCCTGCC	1102
rs779789935	in-del	-/AT			intron-variant	RCBTB2	GRCh38.p7	13:48518473	CAAAAAAAAAAAAAA[-/AT]ATATATATATATATA	1102
rs779797133	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48527974	AATCAGTATTAATCA[C/G]TGTATCTGCTACACA	1102
rs779847325	snp	A/G	1.71296e-05	0.00292652	intron-variant	RCBTB2	GRCh38.p7	13:48501904	CTTCCAGAGTTAGCT[A/G]CAGACATAATGAACA	1102
rs779852598	snp	A/C	1.64749e-05	0.00287005	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510714	AAGAATTGGCGCCCC[A/C]AGCATACACTTGGCC	1102
rs779876061	snp	A/G	3.37844e-05	0.00410987	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502739	CCACGGAGAGGAGGC[A/G]CCACGTGACGGCGGG	1102
rs779905601	snp	A/G	1.73899e-05	0.00294867	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496218	CTTCACCGCAGCCGA[A/G]AGCAGAGCGATGGCA	1102
rs779972152	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48515837	GAACACTGGTTTTGG[A/G]AGGAACACACTGCAT	1102
rs780029929	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48498632	CTACTCGAGAGGCTG[A/C]GGCAGGAGAATCGCT	1102
rs780037964	snp	A/G	1.69178e-05	0.00290837	intron-variant	RCBTB2	GRCh38.p7	13:48490303	ATTTACTAATTCAAT[A/G]CAACATAGCATGAAA	1102
rs780041101	snp	C/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511795	CGGATGCCTTGCAAA[C/G]CTGCCACTCTGCAAG	1102
rs780057817	snp	C/T			intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504261	ATCCTCTTGGAACAC[C/T]GTTCTCATCAGAACT	1102
rs780070555	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528660	AGCTTTTTAAGGGTC[A/G]TCTTCAAGTTATAAA	1102
rs780083437	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48511389	CTGTTACACCTATTT[C/T]TTTTATTAAAGTTAT	1102
rs780123481	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499680	TATTCCAGGAAGGCC[C/T]GGTAAACAGGATATG	1102
rs780159843	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48525942	GGCTAGACTTTGATG[A/G]GAATTTTTTCGTGGG	1102
rs780162843	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48531154	CTAGAATGTAAGCTC[C/G]AGAGGGAAGGGATCT	1102
rs780168286	snp	C/T	1.64836e-05	0.0028708	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512866	CCAGCTGGCTATAAG[C/T]ATTATGACCCCAGGT	1102
rs780175586	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48513061	GAATCTATTTGGAAA[C/G]TATAAACTGCATTCT	1102
rs780457571	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48525084	AAAAGAGAATCCATG[C/T]GGAAATGTAAAAAAA	1102
rs780519349	snp	C/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488841	CTATGAGACTTTATC[C/T]GAGTAACTGCTTGAT	1102
rs780529263	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48498878	ACCTCAGTGCAGCCA[A/T]CCTTCTCTCTCAACT	1102
rs780534515	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532104	GCGTTTTGTTATAGT[C/G]CTGGTCTCGAACTGT	1102
rs780554654	snp	G/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501732	AATTCTCAAATAAAT[G/T]ATTCCTTACCGAATC	1102
rs780650694	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48529015	TTCAACAAGAGTGAT[A/G]AGTCAGATCTTCAGT	1102
rs780653462	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497516	TTACAGGATTTGTAA[C/T]TAGCATAAAGAATGT	1102
rs780740988	snp	A/C/T			intron-variant	RCBTB2	GRCh38.p7	13:48494803	TGTAAGTGCCCAATA[A/C/T]GTTATTGCCTTGATA	1102
rs780801094	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48517735	TAGCTAAAAAGAGCT[A/C]AAAAGATAGTTTTCT	1102
rs780910590	snp	C/T	0.00018558	0.00963098	intron-variant	RCBTB2	GRCh38.p7	13:48522303	AGGAAAAATAAATTT[C/T]AGACCTTTGTCAACT	1102
rs780995642	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505199	CTTGGTTTCATCACA[C/T]TGCAAGGGTGGTGTG	1102
rs781011076	snp	C/T	3.29527e-05	0.00405898	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512089	ACTTTATTTTGTAGG[C/T]AGCCAGTGACTCTTC	1102
rs781078733	snp	C/T	8.25962e-05	0.00642583	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515700	AATTGGCCACTTTCC[C/T]ACATCTAACATCTTC	1102
rs781101981	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518148	CTCCAGAACTGTGAG[A/T]AAAGAAATTTCTGTT	1102
rs781153358	snp	G/T	1.64741e-05	0.00286998	stop-lost, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490111	TTCCTGCAGATGGGA[G/T]CAATTTTTAAAGGCT	1102
rs781184217	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528842	AATTATAAACAGGAC[A/G]GACAAAACTAAAACA	1102
rs781263556	snp	C/T	1.68218e-05	0.00290011	intron-variant	RCBTB2	GRCh38.p7	13:48510817	AAATATAAGTAATTA[C/T]TTCACTGCTTCCACA	1102
rs781271841	snp	C/T	1.6476e-05	0.00287014	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510731	GCATACACTTGGCCT[C/T]CATCTGTTAATACTA	1102
rs781279741	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48513499	ATCATACAGTTTGTA[C/T]TCATTTCATCTGTAT	1102
rs781342227	in-del	-/T	1.64765e-05	0.00287019	frameshift-variant, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510742	GCCTTCATCTGTTAA[-/T]ACTAATGTGTGTGCG	1102
rs781469674	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48490321	ACATAGCATGAAAAT[C/T]GCTAAAACAAGTTAG	1102
rs781483591	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48527517	GCCTTGCAATATAAA[C/T]AGAAAATGGAATGAT	1102
rs781556810	snp	G/T	1.69232e-05	0.00290883	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496247	CATTCTCCTCGCAGA[G/T]GCCTTGCTTGATAGT	1102
rs781582732	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48532791	CCTGCGGCCTGGGCT[C/G]GGTGTAGCCCCGGAA	1102
rs781656362	snp	G/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488877	CATAATATATCCAAT[G/T]TATTTATGTACATCT	1102
rs781656505	snp	G/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503520	TCTAAGTTCACGATT[G/T]ATGAGGAGGTAATTC	1102
rs781734585	snp	A/C/G			intron-variant	RCBTB2	GRCh38.p7	13:48508306	CCTCGGAATACGCCC[A/C/G]TGATTGAGTGCCTGG	1102
rs781740063	snp	C/T	1.70729e-05	0.00292167	intron-variant	RCBTB2	GRCh38.p7	13:48515582	TTATTTTCTTCAAAA[C/T]TACCTCATCATTTAC	1102
rs796103797	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48518195	TTTGTTACAGCAGCA[C/T]AAAGAAACTAACAGA	1102
rs796139091	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48509593	CCCAATTCTGAAGGG[A/G]CCAGGGGTCTTAAAT	1102
rs796196291	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48525742	GGCATATGCATACTA[C/T]ATAGCTATTAAAATA	1102
rs796246316	in-del	ACACACACA/TCTCTCTCTCT			intron-variant	RCBTB2	GRCh38.p7	13:48493317	ACACACACACACACT[ACACACACA/TCTCTCTCTCT]TCTCTCTCTCTCTTC	1102
rs796249372	snp	G/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488665	GGGCATGAGGCATAA[G/T]GGAAAACTGTGTTTT	1102
rs796418638	snp	C/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48504127	TTGTAATGTCTCCCC[C/T]CAGCCACCACTGGGG	1102
rs796481076	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48498731	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAATTA	1102
rs796489522	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506236	CAGGGACGGAGGCCA[A/G]CGCCGGGATCGGAGG	1102
rs796517223	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48510267	TCCTAAGCCAGGGAA[G/T]AGCGACCTTGAATGT	1102
rs796520878	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48497133	AATTTGATATGGTTG[A/C]TAATGCTCTCCTTAG	1102
rs796589749	in-del	A/TCTCT			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499144	ACACACACACACACT[A/TCTCT]TCTCTCTCTCTCTCT	1102
rs796624132	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48497734	TGCTAATAAATCTTA[C/T]ACATGTGGTAGACTT	1102
rs796680439	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48490639	TTATATTTATATCAG[A/C]GTCTTTAAGTATGTC	1102
rs796682403	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529070	AAAAGATTACTGAGC[C/T]TGACAACTTCAGTCT	1102
rs796763303	in-del	-/AG			intron-variant	RCBTB2	GRCh38.p7	13:48531429	CGAACCAGCAGTACA[-/AG]AGTTTGGAGAGCCAG	1102
rs796811448	in-del	A/CC			intron-variant	RCBTB2	GRCh38.p7	13:48532570	CGGGACCTGTGACGC[A/CC]CCCCAGCCACACCAG	1102
rs796814213	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48520704	TACCTGTATAACTAT[C/G]CTTCTCCAGCAATAT	1102
rs796928262	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48508550	CTGGGATTACAGGCA[-/T]GTGCCACTGTGCCCA	1102
rs796999912	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489836	AGGGTACCAAAGGTG[C/T]CCAATTTAAGTGACT	1102

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