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

FBXO22

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs565602234	in-del	-/C			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935595	CTAGAAATAGATCCA[-/C]CCTTGCAGACTGATA	26263
rs565677445	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929979	CAGCAAGTAGTCAGC[A/G]CTTTCAGTGATATGA	26263
rs565739842	snp	A/G	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75929254	GAGCCCACGTGGATA[A/G]ACCAGATGATTTAAT	26263
rs565945295	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905261	TGTCTTGCTCAGTGA[A/G]CACACCTAGAAAGCC	26263
rs566020241	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908266	CCTAAATCTGTTTTT[G/T]GTTTTGTTTGGTTTT	26263
rs566032580	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75908149	GATGCCTCATAAACT[C/G]TCAGGACCAGACTTT	26263
rs566193102	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911301	TCTCACTCTGTGAAG[A/G]AAGTCAGTGGTAGCT	26263
rs566210254	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903603	ACAAAAATTAGCTGG[G/T]CGTGGTGGCGGGAGC	26263
rs566213201	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914284	GAGTTATTTTTAGCT[C/T]AGAACCACATTTCTA	26263
rs566230397	in-del	-/AG	0.00119737	0.0244387	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902677	ATCGGTTTTTTAAAA[-/AG]AGTTAAGCATTAAGA	26263
rs566243164	snp	A/C	0.00361382	0.0423539	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904005	GTGCCGCGGCTCCTC[A/C]GTAGACCCGCGGAGC	26263
rs566304143	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75907615	AATATTTTAAAGTCC[A/G]CCAGGCATGGTGGCT	26263
rs566367066	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915105	CCCAAGTAGCTGGGA[A/T]CACAGGCGCCCGCCA	26263
rs566475079	snp	A/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932314	TGTAAACAATAGCAG[A/G]AGGCTTCGTTTAGTG	26263
rs566591482	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919801	TCAGAAGCCACATGC[C/T]AGAGGAGCATACATG	26263
rs566592248	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910825	TTGGTGTTTTAGTCA[C/T]GAAGTCTTTGCCCAT	26263
rs566659696	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918227	CTGGAGTAAAAAATT[G/T]TGTAGCAGCAAAGGT	26263
rs566712746	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927806	ATTGGTCATTCACGC[A/T]TCTGCATACCCTTTG	26263
rs566727463	snp	C/T	6.07232e-05	0.0055098	intron-variant	FBXO22	GRCh38.p7	15:75917423	ATTTATCATTAACTG[C/T]TCATTTTATTGATTA	26263
rs566736140	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926942	TGCAATGGACATTAT[C/G]AGTGTGGAATTGAAC	26263
rs566748197	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75917999	AGCTTGGATGGGAAA[A/G]CTTAACTTAATATAG	26263
rs566751437	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928246	CAGCAGTCCTATTAC[C/T]GGGTATATATTCAAA	26263
rs566765715	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910039	TTCTGTTCCTGTGTT[A/T]GTTTGCTGAAAATGA	26263
rs567012403	snp	C/G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929146	TTTTTCTCTTCCTAC[C/G/T]GCTCCAGTTTCTGCT	26263
rs567082498	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919196	AGGGTGGTCTCAAAC[C/T]CCTGGCCTCAAGTGA	26263
rs567392193	snp	C/T	7.03618e-05	0.00593093	intron-variant	FBXO22	GRCh38.p7	15:75913342	TTATCATGTGCCTTC[C/T]GTTCGGAGTTCAATA	26263
rs567415392	snp	C/T	0.00953873	0.0683987	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934773	ATATAGCCCATAAGG[C/T]AAATATTTTTTAAAC	26263
rs567427307	snp	A/G	1.68125e-05	0.00289931	intron-variant	FBXO22	GRCh38.p7	15:75914080	CTTTAAATGGATGAT[A/G]TTTATCATTTTGCTA	26263
rs567514558	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919957	ATTTTTGATGAGGAA[A/G]CTGAACTTTAATGGC	26263
rs567551332	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920613	GATCGCTTGAGCCCA[A/G]GAGTTCGAGACCAGC	26263
rs567573842	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911712	ATGTCATCTGCAAAC[A/G]GAGACAATTTGAATT	26263
rs567603214	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903063	AAACTTAGTAGTTTC[C/G]AGGTGAATCTGATGT	26263
rs567662534	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75905346	TTCTCTGGCCCCCAA[C/T]TTCAAAAGGGGAGCC	26263
rs567696519	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906244	GTCCTGGAATTGGCC[A/G]TTAAGCCCTGGCTCC	26263
rs567773739	snp	C/T			synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932940	TAGAAAGTTTTTTCC[C/T]AGTGTTCCCTTATTC	26263
rs567786859	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75916504	GATTAGGGTCCTACC[C/T]TTGTGACCTCATTTA	26263
rs567820722	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928365	GAATGCCCATCAGTG[A/G]TAAACTGGATAAAGA	26263
rs567842683	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929147	TTTTCTCTTCCTACC[A/G]CTCCAGTTTCTGCTT	26263
rs567925330	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915285	GCTGTTATGTTTTTT[C/T]GTTCCAACTCAGTAG	26263
rs568092454	snp	G/T	0.00478085	0.0486577	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902250	GATGCCAGTGAGCTT[G/T]CTTTAGGGAGAGGAT	26263
rs568323724	in-del	-/AAA			intron-variant	FBXO22	GRCh38.p7	15:75916056	TAAGACTCTGTCTCC[-/AAA]AAAAAAAAAAAAAAA	26263
rs568424392	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934588	ATTTATATATATATG[A/C]TAAAAATGCTTGGAA	26263
rs568464658	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75927038	TTTTGAGGCCAGCAA[A/G]GATTTTCCTTATGAA	26263
rs568559512	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903510	TCTGTAATTCCAGCA[C/T]CTTGGGAGGCCCAGG	26263
rs568621700	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910538	GATGAGCTTCTTTTC[A/G]TATGTTTGTTGGCCA	26263
rs568642032	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902549	AAAAAAAGAAAAAAA[A/C]CACAGCTACTCAGGA	26263
rs568642581	snp	A/G	0.0158469	0.0875917	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930177	AGTTCATTCCATTTT[A/G]TAGTAGACATTGGCT	26263
rs568747383	snp	C/G	4.96339e-05	0.00498142	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917303	TTTTGCTTTATTATT[C/G]CCTCAAATTGAAGGA	26263
rs568952696	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926233	TGGGTCCTTGATGAT[C/T]CTTTACCTATGAATT	26263
rs569092892	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925471	GGTAAAATAGAACTT[C/T]AATGACTTGTCAGAT	26263
rs569120508	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902354	TCAGGAAGCTCTGGT[A/G]ACATCTGGGCCATCT	26263
rs569131406	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933595	ATTTTTTCAGAAGTA[A/G]CAATATTATTATTGA	26263
rs569204649	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75927350	ATATTCAGGTAGGAT[A/G]TTTAGTGGATGTTGT	26263
rs569245709	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929520	TAAACCAGTGTTTTT[G/T]TTTTTTTGTTCCCTA	26263
rs569313464	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911810	ACTATGTTGAATAGG[A/G]ATGGTGAGAGAGGGC	26263
rs569583015	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923897	AAGATGAAGTTTGGG[A/G]CTGAATGGACAGGAT	26263
rs569773079	snp	C/G	3.31559e-05	0.00407147	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930103	GGGAAATGGTCTCAG[C/G]TTTTGTCACTTTGGG	26263
rs569823433	in-del	-/AAC	0.00159617	0.0282053	cds-indel, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933594	AATTTTTTCAGAAGT[-/AAC]AATATTATTATTGAC	26263
rs570037314	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902159	CGGGGGAGGTATGAA[A/C]GGCATGCACAGACTG	26263
rs570051797	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932663	GTTTCATGAGATATT[A/G]CCACTTTTCTAAATT	26263
rs570338336	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75915736	GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT	26263
rs570340098	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907672	AAGCCGAGGCAGGCA[A/G]ATCACTTGAGGTCAG	26263
rs570341945	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931648	CATTTTATAGATTCA[A/G]ATGTTGGAAGCATGA	26263
rs570374682	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75908327	GCCCAGGCTGGATTG[C/T]AGTGGCCCGATCTTG	26263
rs570409222	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75912398	TGAATTCGTCTGGTC[C/G]TGGGCTTTTTTTGGT	26263
rs570501669	snp	A/G	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75908391	GATTGTCCTGCCTCA[A/G]CCTCCTGAGTAGTTG	26263
rs570527480	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75915769	GCCAGGCATGATGGC[A/G]GGCACCTGTAATCCC	26263
rs570579207	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923039	GGCCAAACCTTTTGT[C/G]TGCTGCCTTTTTTGT	26263
rs570847347	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933780	AGACCAGAGTATTAC[A/C]TCATCTTATTTTGGT	26263
rs570911962	snp	C/T	8.23676e-05	0.00641693	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932844	CATTCCAGAGCATAA[C/T]ACCATTGGCTTCATG	26263
rs571285940	in-del	-/ATC	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75926051	TTTTGTAACCAGCTT[-/ATC]ATCTTGAAAGGTTCA	26263
rs571294792	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75929230	ATGAGGACACTGTCA[C/T]TGGATTTAGAGCCCA	26263
rs571305296	in-del	-/CTAT	0.00199481	0.0315187	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902590	ACTGACAATGTCATA[-/CTAT]CCACCAGTGGGGGAA	26263
rs571312735	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923658	TTTTGGAGTACAAGA[A/G]TGGATGCAGGATTAG	26263
rs571386153	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906341	GGATTTGCTGCTCCA[A/G]AGCCCAGTCATTAGA	26263
rs571538733	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912503	TTAGTGTTGGAAGGG[A/G]GTATGTGTCCAGGAA	26263
rs571542893	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904274	CCCAGCCGTGGTGCC[C/T]CGGGGGGACTTCCCT	26263
rs571576794	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904692	CAGTCTTTGAGAACT[A/T]TTTTTTTTTAAATCC	26263
rs571778932	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75904253	CCCCCTACCCGCGAG[G/T]TATCTCCCAGCCGTG	26263
rs571840374	snp	A/T			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932472	GTATTTGTGACTGAA[A/T]AAAATGGTGGCTTCT	26263
rs571848319	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913474	GCTTCAGATTGATTT[A/C]TAAACCTTGTAGTGC	26263
rs571849942	snp	A/G	0.000578823	0.0170023	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914199	ATTGTGACCCCAGGA[A/G]TTGTAGGTGAGATAA	26263
rs571875059	in-del	-/ATGTCATACT			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902582	CTTATGCCACTGACA[-/ATGTCATACT]ATCCACCAGTGGGGG	26263
rs571942313	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912979	GTCCTTGTTCTCATT[A/G]GTTTCAAAGAACCTC	26263
rs571980992	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75905044	TAGCCAGAATGGTCT[C/T]GATCTCCTGACCTCG	26263
rs572047906	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75931599	ACTTAACCTTTTTGC[A/G]TCTTAGTTTCTCACT	26263
rs572067645	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921099	ACAAACATGGACAGC[A/G]TGTTACTGTACTGAA	26263
rs572160170	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75905438	CTGGGGAGTGGAAGG[A/G]AACCATTTGACAGTA	26263
rs572223838	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934433	ACTAATGTTACTTTT[C/G]TAACAGTCAGTGGTT	26263
rs572292841	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928746	AAAAAAAAAATCAAA[G/T]TGATAGTCTATAAAC	26263
rs572391924	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930346	ACTCTGTGTGACCTC[A/T]ATGTGTCACCTCCTT	26263
rs572804086	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902366	GGTGACATCTGGGCC[A/G]TCTGGCTTCCTTAAG	26263
rs572827267	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75909125	TTTCATTTAATTCAG[C/T]TGCTTTGCCGCTTGT	26263
rs573161397	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927173	CACAGGGTTGTGAAG[C/T]AGCAATATTAATTTG	26263
rs573254473	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911913	GTTTGTCATAAATAG[C/G]TCTTATTATTTTGAG	26263
rs573321748	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918735	TGTTAAGTGAAATAA[A/G]CCAGGCCCAGAAAGA	26263
rs573343275	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903812	ACGGGCTCCAGACGA[A/G]GGAACGCACCGGCGT	26263
rs573347262	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75918659	ATACATACATAATGA[A/G]ATACTCTTCAGCCAT	26263
rs573386040	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911359	TTACTTTGGGCAATA[A/T]GGGCATTTTCACGAT	26263
rs573442607	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917969	TGAAGAGGTAAAGGG[C/T]TGGCTTAATGTCTAA	26263
rs573459127	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920070	CTTCCTTTGGGAAAA[G/T]GTCAGATAGTGCCCT	26263
rs573600600	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927932	ATTAGATTCATTTTC[A/C]TGTCCCCAAAGCACC	26263
rs573697865	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75935015	CTGAGCCTTTGGAGC[C/T]TGTTATGAACAGTAA	26263
rs573823953	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902961	AGCATGCATCAGAAT[C/T]GTCATAAAGTGTGTT	26263
rs573887354	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903643	AAGCTACGAGGGAGG[C/G]TGAGGCGGGAGGATC	26263
rs573895652	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912071	TATATGTTTATATGA[C/T]GTGTATTGATTTGCA	26263
rs573933261	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75912914	TTTAGTGCTATAAAT[G/T]TCCCTGTAAACACTG	26263
rs573953116	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75919377	TTAGACTTAGCCCTT[C/T]CACAATGTATATATA	26263
rs574054105	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904820	ACCGTTCATCAAATG[C/T]TGGGCCTTTTTTTTT	26263
rs574216272	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934765	ATGTGCTCATATAGC[C/T]CATAAGGCAAATATT	26263
rs574325906	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915932	TAAAATTAGCTGGGC[A/C]TGGTGGCTCATGCCT	26263
rs574352228	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923266	TTGCATTATAGTGCC[A/G]AGTATAGGAATGAGA	26263
rs574391541	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75905680	CTGTTTCTTTAATCT[C/G]CTTTGATCTGGAACA	26263
rs574421077	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908428	CAGGCGCATGCAGCC[A/G]TACCCGGTTACTTTT	26263
rs574455308	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901948	AATTAAATATTTGCA[A/G]AAATGTAGTGATGCC	26263
rs574606290	snp	A/T	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75907955	TCTCAAAAAAAAAAA[A/T]TTTTTTTAAAGTCCA	26263
rs574621362	in-del	-/AG	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75906950	TTTAAAAGTGAAAAC[-/AG]ATTATGAAATTATAT	26263
rs574773129	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75910163	TTCTTCATCCAGTCT[A/G]TCACTGATGGGCATT	26263
rs574775705	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909176	TGAAAACAGGTGAGT[C/T]TGAATAAGCCCAGCT	26263
rs574911306	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933170	AAATGGAAACTTGGG[A/C]CATGTGTATTTCAAA	26263
rs575068756	snp	G/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75924821	CCTTTGAGAATGCTT[G/T]AGGTGGTTAGTTATA	26263
rs575122148	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932391	AGTCAGAAAGGTAAG[C/G]AAACTGTACTTTCTA	26263
rs575161590	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916020	AGGTTGCACCACTTC[A/G]CTCCAGCCTGGGTGA	26263
rs575181521	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908498	GGCTGGTCTCACCCT[C/G]GCCTCAGGCAATCCA	26263
rs575195636	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75924532	GGAGGCATCTTTGGA[A/T]CGCTTTGCCCACCAA	26263
rs575408512	in-del	-/A			intron-variant	FBXO22	GRCh38.p7	15:75916119	AATAGTTATTTTTAG[-/A]AAAAAAAAATTAGAA	26263
rs575722119	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934571	AATATTTTTCTCTTG[C/T]TATTTATATATATAT	26263
rs575741732	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926660	GGGCGTATCCGGGAA[A/C]AACACTAGTCACAAA	26263
rs575772563	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910281	CCTTTGGGTATATAC[C/T]CAGTAATGGGATTGC	26263
rs575811536	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911321	CAGTGGTAGCTTGAT[A/G]GGGATAGCATTGAAT	26263
rs575811569	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903061	TAAAACTTAGTAGTT[G/T]CCAGGTGAATCTGAT	26263
rs575851331	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925932	ACAGTTTCATCCTAT[G/T]CCAAAACCAAAGACA	26263
rs575945531	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905825	CTGTGCTTTTTTCAC[A/G]GCATACTTTAGGTGG	26263
rs576054983	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915492	TCTTTTTGGCCTGGC[A/G]TGGTGGCTGACACCT	26263
rs576105482	snp	C/T	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75914632	GTTTACAGCATGAGG[C/T]TGTGCCCCTTTCCAT	26263
rs576143730	snp	A/G/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933471	ACTACCCCTTGCGTT[A/G/T]TTAGGTGATGTCTTT	26263
rs576166546	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913788	CAAATAGTAGTTATA[C/T]TGCAATATCAGCTGA	26263
rs576212094	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928832	TCTCTGTTACACTCT[A/G]CCACCTCCTAGCGGT	26263
rs576279055	snp	A/G			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931008	AAGGCCAAGTACGTT[A/G]AATCCCAGGCAGGAT	26263
rs576350285	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75932140	GATTGCTTTATCCCA[C/T]GAGTTTGAGGCTGCA	26263
rs576377655	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923335	TGTGAAGCTTTCTTA[C/T]AGGTGTCCTTTCCTG	26263
rs576388301	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75924533	GAGGCATCTTTGGAA[C/T]GCTTTGCCCACCAAA	26263
rs576436143	snp	G/T	0.000798403	0.0199641	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931351	TGTCAGTGGTTAAGA[G/T]AAACCATTGAGTAAA	26263
rs576608206	in-del	-/A			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903372	AGGAATTTGTGAATT[-/A]AGAGAAAGATGTAAA	26263
rs576677200	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930158	AAAGAATTATTAAGA[C/T]AATAGTTCATTCCAT	26263
rs576833415	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915366	TGAATTTGAGTCTTA[C/T]ACAGTGAGGTAAAAA	26263
rs576949846	in-del	-/C	0.00279162	0.0372561	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901922	GAATCTATTTGTCTT[-/C]TATTAAGACAAATTA	26263
rs576957184	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922261	TGGCACCACTGTTGC[A/G]TATGCTTACTGTGCG	26263
rs577015935	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75921320	GCCCTGTATACTACT[A/G]TATAGTTTATAAACA	26263
rs577198363	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916649	ATATCTACCTGTAAA[A/G]TTCAGAGCATATTAC	26263
rs577244046	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912149	GGTAGATAAGCTTTT[G/T]GATGTGCTGCTGGAT	26263
rs577363558	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75924717	CTCTACCTGTCTGTA[C/T]CACAGACAGGAGAGC	26263
rs577489992	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931472	TGTATATTAACAATT[C/G]TGTACCAAAGAGGAA	26263
rs577554005	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919488	AAAGATTGCAGGCTT[G/T]TAGCTACTCTAGTTC	26263
rs577598359	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920051	CTAAATTAAGGATGC[C/G]AAACTTCCTTTGGGA	26263
rs577628666	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929581	AGAGTTGCTGCTCAG[C/T]ACATAGCTGCTTCAT	26263
rs577705224	snp	A/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75928644	GGAGAATGGGCTTAT[A/T]ACCTGGGTGATGAAA	26263
rs577762314	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75916273	CTACTGTGTTAGTCT[A/G]CTAGGGCTACCATAA	26263
rs577854509	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75905636	GGCAAAAAGATCTGT[C/T]CCCAATTGCAATTTG	26263
rs577918283	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904953	CTCAGCCTCCCGAGT[A/G]GCTGGGACTACAGGC	26263
rs578033574	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75924799	TGAGAGCCAGAGCCT[C/G]TTTGCTCCTTTGAGA	26263
rs578132303	snp	C/T	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75905553	GGAAATTATCACTGA[C/T]ACATTTCTACCATTT	26263
rs745366610	snp	A/C	1.64749e-05	0.00287005	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932815	GCTGCGATGCAGCGC[A/C]TCAAAGCGGCCAACA	26263
rs745564407	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932915	AGGGGAATGTTGAGG[C/T]TGATGCATTTAGAAA	26263
rs745627485	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75924219	CTGGCTTCAGTGATT[C/T]GAGGAGGAGGGCCGG	26263
rs745873435	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75911666	AAGGAGATTTTGGGC[C/T]GAGATGACTGGGTTT	26263
rs745878527	snp	A/C/G	3.34769e-05	0.00409115	intron-variant	FBXO22	GRCh38.p7	15:75914229	AATTAGCAACTTGAT[A/C/G]ATTTCTTCCTTGCAT	26263
rs745905156	snp	C/T	6.37288e-05	0.0056445	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904007	GCCGCGGCTCCTCCG[C/T]AGACCCGCGGAGCAC	26263
rs745962957	snp	C/T	9.97158e-05	0.00706031	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903950	TAGGACTGGTTCCGG[C/T]GGGCTGGTGAGGAAT	26263
rs745972871	in-del	-/T	1.65337e-05	0.00287517	intron-variant	FBXO22	GRCh38.p7	15:75917212	CTATTGGTGAAACTG[-/T]TTTAACTTTTTCTCT	26263
rs745980642	snp	A/G	1.81004e-05	0.0030083	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932660	AATGTTTCATGAGAT[A/G]TTGCCACTTTTCTAA	26263
rs746063272	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75918712	CCAGCATGGATGAAC[A/C]TGGAGGATGTTAAGT	26263
rs746067328	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933832	GTGGAACTCATTCAG[A/G]TAATGTTTTGCATTT	26263
rs746244367	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902388	TTCCTTAAGCAGCTG[C/T]GCCTATAAATAGACT	26263
rs746420956	snp	A/G	1.64817e-05	0.00287064	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75930047	ATCACTGACTTCTGA[A/G]AAGTATGTCTTGTGT	26263
rs746467600	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903508	TGTCTGTAATTCCAG[C/T]ACCTTGGGAGGCCCA	26263
rs746627773	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75924352	ACTCAGTAAGGATCT[C/T]CTTGAGCCATTTCTT	26263
rs746675910	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75925959	GACATCTCTTGGTGG[A/C]CAACTACAGTAGTTA	26263
rs746771683	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75911799	GAACCTCCAATACTA[C/T]GTTGAATAGGAATGG	26263
rs746891587	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75913346	CATGTGCCTTCCGTT[C/G]GGAGTTCAATATTAT	26263
rs746996731	snp	A/T	1.65886e-05	0.00287993	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913247	TTACATGGCTGATTC[A/T]GAAACTTTCATTAGT	26263
rs747053593	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75913569	TTTTTATTATTAAAA[C/T]AGGTTGTATGACTTG	26263
rs747068868	snp	A/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75935021	CTTTGGAGCTTGTTA[A/T]GAACAGTAAAATCAT	26263
rs747140569	in-del	-/TC	6.606e-05	0.00574679	intron-variant	FBXO22	GRCh38.p7	15:75929838	ATGTATAAAATAATT[-/TC]TGTTTTAAGGCTGTC	26263
rs747165436	snp	C/T	0.000127494	0.00798316	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904002	CGAGTGCCGCGGCTC[C/T]TCCGTAGACCCGCGG	26263
rs747304619	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906450	ATATTTCTATATATA[C/T]GTGGAGGCTCATGAG	26263
rs747310048	snp	A/G	0.000223739	0.0105745	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903938	TCCGAGCCGCCGTAG[A/G]ACTGGTTCCGGCGGG	26263
rs747317087	snp	A/C/G	3.30793e-05	0.00406679	intron-variant	FBXO22	GRCh38.p7	15:75904651	AGCAAGGGGTGTCAT[A/C/G]CACAGTCATTTGCAG	26263
rs747375115	in-del	-/AATA			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933256	ATGAGGGTAGTATTT[-/AATA]AATATATTAGATGAA	26263
rs747493804	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75929406	CCTTTGGCATGGGCA[A/G]GGGGCACTGTTCACC	26263
rs747555820	snp	G/T	1.66366e-05	0.0028841	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913228	TCTTACCACATACAG[G/T]TCTTTACATGGCTGA	26263
rs747617597	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75926094	ACACTGTTTAAAGTG[A/C]CTTATAAATACTTTT	26263
rs747618087	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915254	GGATTACAGGCATGA[A/G]CCACTGCACCTGGCT	26263
rs747892793	snp	A/G	1.70356e-05	0.00291848	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903913	CCCTATGCTGGCGTA[A/G]TCGGGTTCCTCCGAG	26263
rs747985299	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929986	TAGTCAGCACTTTCA[A/G]TGATATGAATATCAT	26263
rs748038935	in-del	-/CA			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903703	GAGCAGAGGCCGCGC[-/CA]CTCCACTCCCGCCTG	26263
rs748060190	snp	A/C			utr-variant-3-prime, nc-transcript-variant	FBXO22, NRG4	GRCh38.p7	15:75935264	GAGTATTAGCTAAAA[A/C]CAAACTAAATTCCTA	26263
rs748130208	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75906600	TTAGATATTACATCA[A/G]TGCCCCATATGTAAC	26263
rs748135980	snp	A/G	1.64849e-05	0.00287092	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933030	GAGGAAATGTAATGA[A/G]GTAAAAGATGATGAT	26263
rs748206628	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922374	GTTCTGTGAGAGCAG[A/G]ATGGGTAGATTGCTG	26263
rs748235286	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75918101	AATTCACTTCATTCA[-/T]TAAAAATCACTGTTG	26263
rs748391485	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932869	TTCATGTTTGCATGC[A/G]TTGGCAGGGGCTTTC	26263
rs748513204	in-del	-/CTC	3.2962e-05	0.00405954	cds-indel, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932761	CAGAGTGCCACTGTG[-/CTC]CTCAACGAGGACGTC	26263
rs748564566	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932801	AGAAGACTGCTGAGG[C/T]TGCGATGCAGCGCCT	26263
rs748613679	in-del	-/TTTGGTTTTTTTTTTT			intron-variant	FBXO22	GRCh38.p7	15:75908273	CTGTTTTTTGTTTTG[-/TTTGGTTTTTTTTTTT]TTTGAGACAGAGTCT	26263
rs748679911	snp	A/T	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933012	CACTGGGAACTTTAT[A/T]TTGAGGAAATGTAAT	26263
rs748724516	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902457	TAATCTCAACGCTTT[A/G]GGAGGCGGAGGCAGA	26263
rs748854482	snp	C/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932917	GGGAATGTTGAGGCT[C/G]ATGCATTTAGAAAGT	26263
rs748859664	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915078	ATTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCA	26263
rs748921842	snp	A/G	1.66638e-05	0.00288645	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913220	TGTTCGCATCTTACC[A/G]CATACAGTTCTTTAC	26263
rs749038086	snp	A/G	1.69885e-05	0.00291444	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917363	GGATCCAAAGAATTT[A/G]ACATTAGAAAGACAT	26263
rs749205549	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922791	TAGGGCATGAGGACT[A/G]GGGAATGAATTGGAG	26263
rs749329307	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75909936	CCCACTCCCTGACAG[G/T]CCCTGGTGTGTGATG	26263
rs749508478	snp	G/T			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931178	AGTTTACCTTTGAAA[G/T]GCAGATACCTCACTC	26263
rs749562094	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75918293	ATACACATTGAGACT[A/G]GTTTTTACAACTATC	26263
rs749604173	snp	C/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932667	CATGAGATATTGCCA[C/G]TTTTCTAAATTTTCC	26263
rs749765379	snp	A/G	0.000106832	0.00730784	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904086	CCTGCCCGCCAAGGC[A/G]TTGCTGCGGGTGGCC	26263
rs749768805	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919336	TTACTACAAAAATGG[C/T]AACTGTGAGATAATG	26263
rs749822521	snp	A/G	4.94271e-05	0.00497102	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932772	TGTGCTCCTCAACGA[A/G]GACGTCAGTGATGAG	26263
rs749853495	snp	C/T	6.3908e-05	0.00565242	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904015	TCCTCCGTAGACCCG[C/T]GGAGCACCTTCGTGT	26263
rs750042912	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933234	TTTGATTGATGCTCT[A/G]AGATCACATGAGGGT	26263
rs750061201	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75917941	TAGTGTGGATGGAGC[C/T]CTGAAGTGAATTTGA	26263
rs750103985	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919146	GCTAATTTTTTTTGT[C/T]TTTTTATTAGAGATA	26263
rs750122494	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75904236	CGCCCTACCTGAGGT[A/G]ACCCCCTACCCGCGA	26263
rs750148512	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903398	GTAAACTCAGAAATA[C/T]GGCGGTGCCAGGGCA	26263
rs750180280	snp	A/G	1.64942e-05	0.00287173	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904621	CGCGTGGTAGCAGAG[A/G]AGCTTGAGGCAAGTA	26263
rs750241219	in-del	-/TG			frameshift-variant, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932723	CGGGTGTGGTTGGAC[-/TG]TCATTTAGTGGACAC	26263
rs750256929	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75905840	GGCATACTTTAGGTG[A/G]CATGTGATTTCCATT	26263
rs750298256	snp	A/G	3.314e-05	0.00407049	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917310	TTATTATTCCCTCAA[A/G]TTGAAGGAATAAAAA	26263
rs750332364	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75910785	AGCTCCTATTTGTCA[A/G]TTTTGGCTTTTGTTG	26263
rs750440992	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75926967	TTGAACAGATTACAG[A/G]CCTAGAGTTACAATT	26263
rs750445737	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932768	CCACTGTGCTCCTCA[A/G]CGAGGACGTCAGTGA	26263
rs750445838	snp	A/G	1.65734e-05	0.00287862	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913266	ACTTTCATTAGTCTG[A/G]AAGAGTGTCGTGGCC	26263
rs750535389	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75914513	TTTGTCAGTTCAAGC[A/T]GTATTGTGTTTGGTG	26263
rs750665707	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75927826	CATACCCTTTGTTTC[C/T]TTAAGTAACTCTCCT	26263
rs750707809	snp	A/G	1.66932e-05	0.002889	intron-variant	FBXO22	GRCh38.p7	15:75913303	GAGGTAAATATCAAA[A/G]GAAAAGCTTTTGCTT	26263
rs750714799	snp	A/C	1.64746e-05	0.00287002	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932846	TTCCAGAGCATAACA[A/C]CATTGGCTTCATGTT	26263
rs750742937	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934822	AACCAGAATTGGTTG[A/C]ATAGTAGAGGAAAAG	26263
rs750748488	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915535	CTTTAGGAGGCCGAG[A/G]CAGGCGGATCACTTG	26263
rs750759263	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75920754	CTTGAGCCCAAGAGG[C/T]GGAGGTTGCCGTGAG	26263
rs750928836	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75922138	TGCTATACTTTTATA[C/T]GACTGGCACTGCAAT	26263
rs750948103	snp	A/G	1.64885e-05	0.00287123	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914164	AGAAGCTATTCCCCA[A/G]ACAATGCCAAGTCCT	26263
rs750951174	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907610	TTAGAAATATTTTAA[A/G]GTCCGCCAGGCATGG	26263
rs751012529	snp	A/G	1.66854e-05	0.00288833	intron-variant	FBXO22	GRCh38.p7	15:75914222	TGAGATAAATTAGCA[A/G]CTTGATGATTTCTTC	26263
rs751016783	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919267	GTGAGCCATCGTGCC[C/T]GGCCCATATACTATA	26263
rs751023950	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923502	CTTCCATATCCATGG[A/G]TTCTGCATTCATGGA	26263
rs751068751	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911615	CTGCACATTGATTTT[A/G]TATCCTGAGACTTTG	26263
rs751105458	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75920406	CCAGGGCAACATAGC[C/T]CAGATTCTGGGAAGA	26263
rs751257161	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75905956	TAATGATTGTTTTGT[C/G]AAGAGATCATTTGAA	26263
rs751316871	snp	C/T	3.47796e-05	0.00416996	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904057	GCGGAGGTGGTGGAG[C/T]GTGTGCTCACCTTCC	26263
rs751507707	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75928371	CCATCAGTGATAAAC[C/T]GGATAAAGAAAATGT	26263
rs751785700	snp	G/T	1.82424e-05	0.00302007	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932643	CTATACTTAAAAATT[G/T]TAATGTTTCATGAGA	26263
rs751786972	in-del	-/AAATT			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901931	GTCTTCTATTAAGAC[-/AAATT]AAATTAAATATTTGC	26263
rs751891331	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75923782	TTTTTTTAAAAAGTA[A/T]ATGCAGGAGACACAG	26263
rs751894349	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75922208	ATGCGTTGTGCTACA[C/T]ATTAGGCAGTAGGAA	26263
rs751916562	snp	A/G	0.000152219	0.00872274	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933699	TTTTATTATAAGTAA[A/G]AGATTTTTCTTCTTT	26263
rs751969919	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75922352	AACCCAAGTGAGTAT[G/T]TGAGGTGTTCTGTGA	26263
rs752006387	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75909306	GAGGTGGCACTTAAG[A/G]TGTCTCTAGAGGGAA	26263
rs752094363	snp	C/T	1.66349e-05	0.00288395	intron-variant	FBXO22	GRCh38.p7	15:75913296	CATAAGAGAGGTAAA[C/T]ATCAAAAGAAAAGCT	26263
rs752134815	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75906057	CAGTGGGATATAATC[A/T]GTTACTGTATTTTGG	26263
rs752165849	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911083	CGTTGTAGATGTGTG[A/G]TGTTATTTCTGAGCC	26263
rs752315696	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75912427	GTTGGTAGGCTATTA[A/G]TTACTGCCTCAATTT	26263
rs752330376	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915277	ACCTGGCTGCTGTTA[C/T]GTTTTTTTGTTCCAA	26263
rs752535106	in-del	-/T	5.07421e-05	0.00503671	intron-variant	FBXO22	GRCh38.p7	15:75913321	AAGCTTTTGCTTCTG[-/T]TTTTTTTATCATGTG	26263
rs752627947	snp	C/T			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935277	AAACAAACTAAATTC[C/T]TAGAGATGACAATCA	26263
rs752654667	snp	C/G	1.70119e-05	0.00291644	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904042	GTGTTGAGTAACCTG[C/G]CGGAGGTGGTGGAGC	26263
rs752667271	snp	A/T	3.34398e-05	0.00408886	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913204	TTTTTTCTTTGCAGA[A/T]TGTTCGCATCTTACC	26263
rs752691849	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75920345	TTGCCTGGCAGTCTG[C/T]CTGTAAAAGCATCAA	26263
rs752714331	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902968	ATCAGAATCGTCATA[A/G]AGTGTGTTAAAACAG	26263
rs752748405	snp	A/G	1.66142e-05	0.00288216	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932719	GCCTCGGGTGTGGTT[A/G]GACTGTCATTTAGTG	26263
rs752835076	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923918	TGGACAGGATGTGGT[A/G]ACTGATGAGATGTTA	26263
rs753018543	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903799	TACACCTCGGAGTAC[C/G]GGCTCCAGACGAGGG	26263
rs753035839	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911325	GGTAGCTTGATGGGG[A/G]TAGCATTGAATCTCT	26263
rs753207047	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933290	CAACTTTGGACATAA[C/T]ACTGACTAGGAGTTG	26263
rs753213331	snp	G/T	1.65282e-05	0.00287469	intron-variant	FBXO22	GRCh38.p7	15:75904644	GGCAAGTAGCAAGGG[G/T]TGTCATGCACAGTCA	26263
rs753274690	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75923079	TGACATAGCTGTTTC[C/T]TGGGCAGTACTCTGT	26263
rs753312397	snp	A/G	3.29473e-05	0.00405864	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932976	CTTTGGAAATGGAGA[A/G]ATTGGATGTGATCGG	26263
rs753324120	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75909279	GGGAGTTTAGGAAAA[C/G]GTTTTGGAGAGGAGG	26263
rs753492995	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75931598	CACTTAACCTTTTTG[C/T]GTCTTAGTTTCTCAC	26263
rs753576180	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75918810	GCTCTCATAGAAATA[C/T]AGAGTTGAATGGCAG	26263
rs753799726	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932953	CCTAGTGTTCCCTTA[C/T]TCGGCTTCTTTGGAA	26263
rs753859755	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75925438	TACTTGTCTTGAATT[C/T]TGCCAGCCACCAAGA	26263
rs753868039	snp	A/G	3.29457e-05	0.00405854	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904522	AGGGAGTGTGTGCGC[A/G]GAGTATTGCGGACCC	26263
rs753877768	snp	A/G			missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904006	TGCCGCGGCTCCTCC[A/G]TAGACCCGCGGAGCA	26263
rs753896326	snp	A/T	0.00013182	0.00811742	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929918	ACTTCGTGTGGTCCT[A/T]GTCTTTGGTTATAAT	26263
rs753948272	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911400	CCTATCCTTGAGCAT[A/G]GAATGTTTTTCCATT	26263
rs753950544	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75926677	ACACTAGTCACAAAC[A/G]AGTGGCTGTGTACTC	26263
rs754003902	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75923765	TTTTCAGTTAAAATA[A/T]TTTTTTTTAAAAAGT	26263
rs754124691	snp	A/G	1.65263e-05	0.00287452	intron-variant	FBXO22	GRCh38.p7	15:75904641	TGAGGCAAGTAGCAA[A/G]GGGTGTCATGCACAG	26263
rs754272711	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934775	ATAGCCCATAAGGCA[A/G]ATATTTTTTAAACTT	26263
rs754341985	snp	C/T	8.23689e-05	0.00641698	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932849	CAGAGCATAACACCA[C/T]TGGCTTCATGTTTGC	26263
rs754458640	snp	G/T	6.71569e-05	0.0057943	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903986	CGGTAGGCTGCTGCG[G/T]CGAGTGCCGCGGCTC	26263
rs754519747	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75904306	AGGGGCGAAGTTCCC[C/T]TTAAGGTTTTCTCCA	26263
rs754525887	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75920456	TACAAGGAAGGAAGA[A/T]GATGATCAATGTGTT	26263
rs754547103	in-del	-/TTT			intron-variant	FBXO22	GRCh38.p7	15:75913322	AAGCTTTTGCTTCTG[-/TTT]TTTTATCATGTGCCT	26263
rs754609613	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75906022	TTTATATCTGTACAC[A/T]CTCGGAGTCTTATTT	26263
rs754706651	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75927327	GAATGGGAGTGGTTG[C/T]CTTTAGAATATTCAG	26263
rs754809023	snp	C/T	3.29538e-05	0.00405904	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929960	GGGAGCCAGTAATTA[C/T]CTGCAGCAAGTAGTC	26263
rs754817638	in-del	-/TT	0.00141332	0.0265455	intron-variant	FBXO22	GRCh38.p7	15:75913183	GGGATCCAATTCCAA[-/TT]TTTTTTTTTTCTTTG	26263
rs754866108	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75928612	GAGGAAGGAGAGGAT[A/C]AGGAAAAATAACTAA	26263
rs754871716	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75914826	AAGTTACCTAACTTC[A/T]TGGGGCTTCACTGTC	26263
rs755071895	snp	A/G/T	3.3055e-05	0.00406529	intron-variant	FBXO22	GRCh38.p7	15:75904643	AGGCAAGTAGCAAGG[A/G/T]GTGTCATGCACAGTC	26263
rs755088177	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932956	AGTGTTCCCTTATTC[A/G]GCTTCTTTGGAAATG	26263
rs755156279	in-del	-/AC			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903257	TTTTCACACACTAAG[-/AC]ACAATTTTTTAAAAG	26263
rs755158121	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75922313	TTGACCAAAGTGTTA[C/T]GTGGTGCTTGACTGC	26263
rs755201876	in-del	-/AG			intron-variant	FBXO22	GRCh38.p7	15:75928551	AATACATCGACGCAA[-/AG]AGGGGCACAACAGAC	26263
rs755276015	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907886	AGATGGAGTTTGCTT[A/G]AGCTGAGATTGCACC	26263
rs755387975	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932850	AGAGCATAACACCAT[C/T]GGCTTCATGTTTGCA	26263
rs755437566	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75909361	GAGCAATAGAACATA[A/T]GGGGAAGTCGGTGTG	26263
rs755509445	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75932104	CTGTAGCCCCAGCTC[C/T]TTGAGAGACTCAGGC	26263
rs755552923	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919851	AATTAACGATGGCCA[A/G]TGTTTATGGAGGTAC	26263
rs755596843	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929912	CCCTGAACTTCGTGT[A/G]GTCCTTGTCTTTGGT	26263
rs755649149	in-del	-/GT			intron-variant	FBXO22	GRCh38.p7	15:75924554	GCCCACCAAAGCACA[-/GT]CTGAAAGCCCCAGCT	26263
rs755657881	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75929006	GGCTGCTGTAACAAA[A/G]TACCCCAAATTTGGT	26263
rs755780709	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933001	GATCGGATAGTCACT[A/G]GGAACTTTATATTGA	26263
rs755816549	snp	C/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930222	ACATAATTCTGCTTA[C/T]GGTTGAATAATTACA	26263
rs755926201	snp	G/T			missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904003	GAGTGCCGCGGCTCC[G/T]CCGTAGACCCGCGGA	26263
rs756012124	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75916171	CTTTAAGCACCACAG[A/G]GTTAACCACTCTTAT	26263
rs756039781	snp	A/C	1.66449e-05	0.00288482	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917327	TGAAGGAATAAAAAT[A/C]CAACCCTTTCATTTT	26263
rs756048669	in-del	-/C	1.74117e-05	0.00295052	intron-variant	FBXO22	GRCh38.p7	15:75913341	TTTATCATGTGCCTT[-/C]CGTTCGGAGTTCAAT	26263
rs756108236	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75923140	TTGATGAGGCCCTGA[C/T]ATGTGGCACTGGTTG	26263
rs756125649	snp	A/C			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903003	CTGGGCCTCACCCCC[A/C]GTGTCTGATTCAGGA	26263
rs756178166	snp	C/T	4.94222e-05	0.00497078	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932847	TCCAGAGCATAACAC[C/T]ATTGGCTTCATGTTT	26263
rs756190837	snp	C/T	4.94328e-05	0.00497131	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932769	CACTGTGCTCCTCAA[C/T]GAGGACGTCAGTGAT	26263
rs756239507	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75923932	TGACTGATGAGATGT[G/T]AGGTGTTGAGAATGA	26263
rs756327669	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75925276	AAACAATACGTAACA[A/G]GTTGTTACAGGCATT	26263
rs756351079	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75909569	GTGCATCTTTTGCTG[A/G]TACTTGATGTTTTTG	26263
rs756518499	snp	A/G	3.34801e-05	0.00409132	intron-variant	FBXO22	GRCh38.p7	15:75913308	AAATATCAAAAGAAA[A/G]GCTTTTGCTTCTGTT	26263
rs756550347	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75918199	CTGTTATTTGAAATG[A/G]GACTTAAACCAGCTG	26263
rs756632086	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919274	ATCGTGCCTGGCCCA[C/T]ATACTATATTCTTGA	26263
rs756762659	snp	C/G	1.67214e-05	0.00289144	intron-variant	FBXO22	GRCh38.p7	15:75914226	ATAAATTAGCAACTT[C/G]ATGATTTCTTCCTTG	26263
rs756855851	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75916344	ATTTTCTCACAGTTT[A/G]GGAGGCTAGAAGTCC	26263
rs756979348	in-del	-/AAAAA			intron-variant	FBXO22	GRCh38.p7	15:75916056	TAAGACTCTGTCTCC[-/AAAAA]AAAAAAAAAAAAAAA	26263
rs757019220	snp	C/G	9.11203e-05	0.00674921	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904063	GTGGTGGAGCGTGTG[C/G]TCACCTTCCTGCCCG	26263
rs757231580	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75904338	ATCTGGCTCTTCTTC[C/G]GAACTAGCGCCCTGA	26263
rs757308718	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933580	TTTCAGTTTTATGAA[-/T]TTTTTTCAGAAGTAA	26263
rs757382367	snp	A/G	1.64825e-05	0.00287071	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932758	ATCCAGAGTGCCACT[A/G]TGCTCCTCAACGAGG	26263
rs757456817	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75913018	TGCCTTTATTTTGTT[A/G]TTTGCCCAGTAGTCA	26263
rs757588474	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933622	TTGACTTTTTACTTA[C/T]TTGATAAAAATTAAA	26263
rs757609524	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75919346	AATGGTAACTGTGAG[A/T]TAATGCATATGTGAA	26263
rs757647110	snp	G/T	0.000276893	0.0117631	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933706	ATAAGTAAAAGATTT[G/T]TCTTCTTTCCTTAAA	26263
rs757686717	snp	A/G	1.67027e-05	0.00288982	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913210	CTTTGCAGAATGTTC[A/G]CATCTTACCACATAC	26263
rs757779836	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75920619	TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTGGAC	26263
rs757873955	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75908304	TTTGAGACAGAGTCT[C/T]GCCTGTCGCCCAGGC	26263
rs758002914	snp	A/G	1.65712e-05	0.00287843	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914204	GACCCCAGGAATTGT[A/G]GGTGAGATAAATTAG	26263
rs758005738	in-del	-/AC			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902737	ATATTGATAGTCATA[-/AC]ACACATAAACTATTG	26263
rs758044222	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919217	CCTCAAGTGATCCAC[C/T]TGCCTCGGCCTCCCA	26263
rs758086588	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75904294	GGGACTTCCCTGAGG[A/G]GCGAAGTTCCCCTTA	26263
rs758132728	snp	A/G	1.82557e-05	0.00302118	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932638	TGCTTCTATACTTAA[A/G]AATTTTAATGTTTCA	26263
rs758176962	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933398	CTTAAATAGTCTTCC[C/T]GCATAGGAAGAGCAA	26263
rs758292404	snp	C/G	1.67894e-05	0.00289731	intron-variant	FBXO22	GRCh38.p7	15:75913310	ATATCAAAAGAAAAG[C/G]TTTTGCTTCTGTTTT	26263
rs758428942	in-del	-/AGAA	3.41568e-05	0.00413246	frameshift-variant, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917369	AAAGAATTTAACATT[-/AGAA]AGACATCAACTCACT	26263
rs758445817	snp	A/G	3.45405e-05	0.00415561	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904051	AACCTGGCGGAGGTG[A/G]TGGAGCGTGTGCTCA	26263
rs758516099	snp	A/C/G/T	0.000100249	0.00707931	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913209	TCTTTGCAGAATGTT[A/C/G/T]GCATCTTACCACATA	26263
rs758594294	snp	A/T	4.94328e-05	0.00497131	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929992	GCACTTTCAGTGATA[A/T]GAATATCATCTTGGC	26263
rs758628507	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934945	CTTCTCAAAGAGTCT[A/G]ATACAGGGTAATTTC	26263
rs758782063	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75919048	CTGCTACTTCTACTT[-/C]CTGGGTTCAAGGGTT	26263
rs758787214	snp	A/G	1.65389e-05	0.00287562	intron-variant	FBXO22	GRCh38.p7	15:75904649	GTAGCAAGGGGTGTC[A/G]TGCACAGTCATTTGC	26263
rs758812767	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932979	TGGAAATGGAGAAAT[C/T]GGATGTGATCGGATA	26263
rs758873976	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915639	AGGCGCAGTGGCTCA[C/T]GTCTGTGGTCCCAGC	26263
rs758882067	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922172	CTTGTTTACAACAGC[A/G]TCACCACAGACATTT	26263
rs758939444	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75907702	GGAGTTAGAGAACAG[C/G]CTGGCCAACATGGTG	26263
rs759080519	snp	A/G	1.69075e-05	0.00290748	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904034	GCACCTTCGTGTTGA[A/G]TAACCTGGCGGAGGT	26263
rs759117543	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75923122	TGAGCATCCTGGGAA[C/T]CTTTGATGAGGCCCT	26263
rs759179130	in-del	-/CTTTC	0.000273486	0.0116905	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933711	TAAAAGATTTTTCTT[-/CTTTC]CTTAAAAATATTTTT	26263
rs759276039	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908793	GGAAATCCACATTTT[A/G]TGTAAAAATTCGGTG	26263
rs759307254	snp	A/G	1.64735e-05	0.00286993	intron-variant	FBXO22	GRCh38.p7	15:75904448	TGTGGGAGAGACGAA[A/G]ATGAACGTCCGTTCG	26263
rs759505244	snp	C/T	1.68915e-05	0.00290611	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930127	CTTTGGGGTTAACAA[C/T]TTAAAAAACGTGTTT	26263
rs759516928	snp	A/G	1.66952e-05	0.00288917	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933079	ACAATAATGGCACTC[A/G]TACATCTGGGGTCAT	26263
rs759651550	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902883	ATTGGCGGGAGGAAT[C/G]GATGTTAGGTGGGGA	26263
rs759717143	snp	C/T	0.00041415	0.0143841	intron-variant	FBXO22	GRCh38.p7	15:75913195	CAATTTTTTTTTTTT[C/T]TTTGCAGAATGTTCG	26263
rs759869116	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903795	GGAGTACACCTCGGA[C/G]TACGGGCTCCAGACG	26263
rs759907497	snp	C/T	1.64972e-05	0.00287199	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917259	TCAGGTAGCAATCGA[C/T]CTCAGGAAATAGAAA	26263
rs759950237	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75926505	GGTTGTGTATTAGGA[A/G]GGGGAAGTGTTCCAT	26263
rs759981603	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75924795	AGCTTGAGAGCCAGA[C/G]CCTCTTTGCTCCTTT	26263
rs759987979	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922555	CAGAGCATGTTGGAG[A/G]AATAGTAATCATTTT	26263
rs760110997	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75911118	GTTCTGTTCCATTGG[A/T]CTGTATATCTGTTTT	26263
rs760121166	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75912238	AAATTTTCTTTTTTT[A/G]TTGTGTCTCTGCCAG	26263
rs760231297	snp	G/T	1.65048e-05	0.00287265	missense, intron-variant	FBXO22	GRCh38.p7	15:75930079	CTTCTGATTTCGTCT[G/T]TGAATGAAGGGAAAT	26263
rs760272039	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923268	GCATTATAGTGCCAA[A/G]TATAGGAATGAGAAA	26263
rs760297427	snp	A/C	1.74051e-05	0.00294996	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932687	CTAAATTTTCCAGGA[A/C]CCCTCTGGATATTGA	26263
rs760298412	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75918027	TAGTAAACAACAAAC[G/T]AATTACTCAAGGAAA	26263
rs760363797	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75908917	CACAGGCCATCATGC[C/T]ATCTGTCTCTTTTAT	26263
rs760427154	snp	A/T	7.11617e-05	0.00596454	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903974	GAGGAATGGAGCCGG[A/T]AGGCTGCTGCGGCGA	26263
rs760473711	snp	A/G	1.65302e-05	0.00287486	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933059	ATCTGTTTCATAGCT[A/G]TACAACAATAATGGC	26263
rs760787385	snp	G/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903908	GGCAACCCTATGCTG[G/T]CGTAATCGGGTTCCT	26263
rs760888424	snp	C/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930112	TCTCAGGTTTTGTCA[C/T]TTTGGGGTTAACAAT	26263
rs760895706	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75910182	CTGATGGGCATTTGA[A/G]TTGGTTTCAAGTCTT	26263
rs760929745	snp	G/T	4.94173e-05	0.00497053	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932943	AAAGTTTTTTCCTAG[G/T]GTTCCCTTATTCGGC	26263
rs760932198	snp	C/G	1.64923e-05	0.00287156	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914172	TTCCCCAAACAATGC[C/G]AAGTCCTTGGGATTG	26263
rs760959208	snp	A/T			intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75905591	AGACTCGGTTCAGAT[A/T]TTGCCAGTTGTCCCA	26263
rs761059005	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75912488	CGACTTCTTCCTGGT[A/T]TAGTGTTGGAAGGGG	26263
rs761281627	snp	A/G	1.64961e-05	0.00287189	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917254	TGGGATCAGGTAGCA[A/G]TCGACCTCAGGAAAT	26263
rs761370582	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75910967	GAAGGGGTCCAGTTT[C/T]AGTTTTCTGCATATG	26263
rs761474958	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933207	TAACTTTAGATATAT[A/C]TTTTTTGTAGCTTTG	26263
rs761493980	snp	C/T	1.64866e-05	0.00287106	intron-variant	FBXO22	GRCh38.p7	15:75929868	TCTTTAACTGTTGCT[C/T]TTCATTTCTCTGCAG	26263
rs761540027	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75912113	AGCCTTGCATCCCAG[A/G]GGTGAAGCCGACTTG	26263
rs761554178	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919060	CTTCCTGGGTTCAAG[A/G]GTTCAAGTGATTGTC	26263
rs761578833	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907832	CCTATAATCGCAGCT[A/G]CTTGGGTAGCTGAGG	26263
rs761593704	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932934	TGCATTTAGAAAGTT[C/T]TTTCCTAGTGTTCCC	26263
rs761610299	snp	A/G	3.29484e-05	0.00405871	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932842	AACATTCCAGAGCAT[A/G]ACACCATTGGCTTCA	26263
rs761635012	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934338	CATTGAAGAAACACC[A/G]TAAGTGGCGTGGACT	26263
rs761667976	snp	C/T	3.29457e-05	0.00405854	intron-variant	FBXO22	GRCh38.p7	15:75904485	TTTGTGCGTTTGCGT[C/T]CTCAGCGTGTGCCGC	26263
rs761709471	snp	A/G	1.64795e-05	0.00287045	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904591	GCCGGCCACCTGGAG[A/G]GGCATTGCTTGGTTC	26263
rs761794804	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919843	GAAGTGACAATTAAC[A/G]ATGGCCAATGTTTAT	26263
rs761815334	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75905731	TTTTTCCCAATCTTG[A/T]CACTTAGGAAAATCA	26263
rs761828873	snp	A/G			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930812	TACTATTTGTTTCCC[A/G]CTCTGTTTAATATTT	26263
rs761921144	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75926850	GAAGAAAGGAAGAAC[C/T]ATTTATGCAGATGTC	26263
rs762010420	snp	C/G	1.64874e-05	0.00287113	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914154	CTTGCCCTTGAGAAG[C/G]TATTCCCCAAACAAT	26263
rs762018895	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75928147	CACTTATACACTGTC[A/G]GTGGGAGTGTAAATT	26263
rs762118114	snp	A/G	3.34644e-05	0.00409036	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904017	CTCCGTAGACCCGCG[A/G]AGCACCTTCGTGTTG	26263
rs762254036	in-del	-/AATT			intron-variant	FBXO22	GRCh38.p7	15:75905891	TACCTTTGATTACTC[-/AATT]AAGGCGATGCTTGCC	26263
rs762488598	snp	C/G	3.29478e-05	0.00405867	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904562	TAACCTGGATCTCCG[C/G]AGGCCTGGCGGAGGC	26263
rs762495928	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933242	ATGCTCTAAGATCAC[A/G]TGAGGGTAGTATTTA	26263
rs762529485	in-del	-/GAT	1.65277e-05	0.00287464	intron-variant	FBXO22	GRCh38.p7	15:75904643	GGCAAGTAGCAAGGG[-/GAT]GTGTCATGCACAGTC	26263
rs762558195	in-del	-/TAAA	0.000579483	0.0170119	frameshift-variant, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933096	ACATCTGGGGTCATC[-/TAAA]TAATAATTAAAGTGG	26263
rs762572053	snp	C/T	1.64735e-05	0.00286993	intron-variant	FBXO22	GRCh38.p7	15:75904458	ACGAAAATGAACGTC[C/T]GTTCGCAATCCTTTG	26263
rs762586914	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934460	GGTTTGTTCTAACAG[A/G]ACAGTAGAACACTTG	26263
rs762620314	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905928	TGTCTTCACTAAAAT[C/T]ACTCTTCTACTGTAA	26263
rs762701171	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75921364	CTACATTAAATTAAT[G/T]GAAACATTTTTGTTT	26263
rs762815161	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75911201	GTCAGGTAGCATGAT[G/T]CCTCCAGCTTTTTTC	26263
rs762981135	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75929748	ATAAAAAATAAAAAA[C/T]GGAAAATTTGATAGC	26263
rs763240952	snp	A/G	1.67083e-05	0.00289031	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903961	CCGGCGGGCTGGTGA[A/G]GAATGGAGCCGGTAG	26263
rs763257481	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902508	GTTTGAGACCAGCCT[A/G]GGCAACATAGACCCT	26263
rs763286719	snp	A/G	3.29848e-05	0.00406095	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914135	AACTAGTATGGAAAC[A/G]GCACTTGCCCTTGAG	26263
rs763397015	in-del	-/TG			intron-variant	FBXO22	GRCh38.p7	15:75911294	AGTTTTTTCTCACTC[-/TG]TGAAGAAAGTCAGTG	26263
rs763411842	in-del	-/TGGGA			intron-variant	FBXO22	GRCh38.p7	15:75919239	GGCCTCCCAAAGTGC[-/TGGGA]TTACAGGTGTGAGCC	26263
rs763512213	snp	C/T	1.8283e-05	0.00302344	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933150	TGGGTTCTGCCTTTT[C/T]CAGAAAATGGAAACT	26263
rs763547167	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75923717	ATATTTCAAAACACC[A/T]TGTTGAACATGATAA	26263
rs763578385	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908918	ACAGGCCATCATGCT[A/G]TCTGTCTCTTTTATT	26263
rs763614594	snp	C/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930321	TGATCTTTCCTTTGA[C/T]AGATGTGGTACTCTG	26263
rs763627414	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907446	TAGTAATGCCCTTAG[A/G]GGAGTTCCTCCATTG	26263
rs763668634	snp	G/T	1.65023e-05	0.00287244	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917276	TCAGGAAATAGAAAT[G/T]GGAGAATCTGGTTTT	26263
rs763675044	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75923373	TGATGTCAGCAGTTT[A/T]GGCTTATTCCAAGGC	26263
rs764026487	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75925176	ACTTTGGTCTGGTCT[-/G]ATCTAGCTTCTGTAA	26263
rs764037110	snp	C/T	3.29462e-05	0.00405857	intron-variant	FBXO22	GRCh38.p7	15:75904476	TCGCAATCCTTTGTG[C/T]GTTTGCGTCCTCAGC	26263
rs764082389	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902157	GGCGGGGGAGGTATG[A/G]ACGGCATGCACAGAC	26263
rs764124123	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932828	GCCTCAAAGCGGCCA[A/G]CATTCCAGAGCATAA	26263
rs764155881	snp	A/G	0.000167364	0.00914626	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904053	CCTGGCGGAGGTGGT[A/G]GAGCGTGTGCTCACC	26263
rs764239822	snp	C/T	6.41993e-05	0.00566529	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904004	AGTGCCGCGGCTCCT[C/T]CGTAGACCCGCGGAG	26263
rs764332883	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75912569	CATAGAGGTGTTTAT[A/G]GTATTCTCTGATGGT	26263
rs764509408	snp	C/G	7.65199e-05	0.00618499	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903967	GGCTGGTGAGGAATG[C/G]AGCCGGTAGGCTGCT	26263
rs764577653	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75914105	TTGCTACTGTATTTT[C/T]ACAGCAAGGAAAAGA	26263
rs764644323	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75926747	AAGGATGGGGAAGGA[C/T]AGGCATGAGGTGAAT	26263
rs764718347	snp	C/G	0.000283166	0.0118955	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933695	AGTATTTTATTATAA[C/G]TAAAAGATTTTTCTT	26263
rs764897997	snp	C/G	7.26085e-05	0.00602486	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904039	TTCGTGTTGAGTAAC[C/G]TGGCGGAGGTGGTGG	26263
rs764961852	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75910775	TAGTTTAATTAGCTC[C/T]TATTTGTCAATTTTG	26263
rs765005512	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919844	AAGTGACAATTAACG[A/G]TGGCCAATGTTTATG	26263
rs765030129	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75905785	TCAATTGTGTCTTTG[G/T]CAGGAAATAATCACA	26263
rs765060986	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919136	ACCATGCCTGGCTAA[C/T]TTTTTTTGTCTTTTT	26263
rs765196400	snp	A/G	1.67478e-05	0.00289372	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932709	GGATATTGATGCCTC[A/G]GGTGTGGTTGGACTG	26263
rs765218008	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75926903	TGATCTCTTGTTTTT[G/T]TGCAGCATCTGGGAA	26263
rs765242141	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934379	AGACTGTTTTACAAG[A/G]GAGAAATTAGCATAT	26263
rs765284356	snp	A/C	3.46831e-05	0.00416417	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930135	TTAACAATTTAAAAA[A/C]CGTGTTTAAAGAATT	26263
rs765315958	snp	A/C	1.65762e-05	0.00287886	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913260	TCAGAAACTTTCATT[A/C]GTCTGGAAGAGTGTC	26263
rs765395506	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75914419	ACCTGTATAAATATC[C/G]AGTAGTCATTCATAA	26263
rs765470562	in-del	-/GCTAGTAGGA			intron-variant	FBXO22	GRCh38.p7	15:75906105	TCACCCCCTAGTTTG[-/GCTAGTAGGA]GCTCCTTCAGGCTGG	26263
rs765523215	snp	C/T	1.67604e-05	0.00289481	intron-variant	FBXO22	GRCh38.p7	15:75913196	AATTTTTTTTTTTTC[C/T]TTGCAGAATGTTCGC	26263
rs765645360	snp	G/T	1.64928e-05	0.00287161	intron-variant	FBXO22	GRCh38.p7	15:75929855	TGTTTTAAGGCTGTC[G/T]TTAACTGTTGCTCTT	26263
rs765742313	in-del	-/ATTT			intron-variant	FBXO22	GRCh38.p7	15:75911005	AGTTTTCTGAACACC[-/ATTT]ATTAAATAGTGAATC	26263
rs765768612	in-del	-/AGGAGGCGGAGGC	0.000121161	0.0077824	intron-variant	FBXO22	GRCh38.p7	15:75904111	TGGCCTGGTGAGGAG[-/AGGAGGCGGAGGC]AGGAGGCGGAGGCGG	26263
rs765777269	snp	A/G	0.000210445	0.0102556	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903975	AGGAATGGAGCCGGT[A/G]GGCTGCTGCGGCGAG	26263
rs765790722	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922112	AAGTATGCATTGTAC[A/G]TGATTGTATGTGCTA	26263
rs765808214	snp	G/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934526	CTGCTTTTCCTTTTT[G/T]GTCACTTTTATCCTT	26263
rs765857687	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933253	TCACATGAGGGTAGT[A/G]TTTAATATATTAGAT	26263
rs765865603	snp	A/T	4.95421e-05	0.00497681	missense, intron-variant	FBXO22	GRCh38.p7	15:75930083	TGATTTCGTCTGTGA[A/T]TGAAGGGAAATGGTC	26263
rs765882635	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919261	ACAGGTGTGAGCCAT[C/T]GTGCCTGGCCCATAT	26263
rs765931064	in-del	-/AAT	1.70842e-05	0.00292264	cds-indel, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933098	ATCTGGGGTCATCTA[-/AAT]AATAATTAAAGTGGC	26263
rs766161392	in-del	-/T/TT	0.298741	0.245729	intron-variant	FBXO22	GRCh38.p7	15:75913182	GGGATCCAATTCCAA[-/T/TT]TTTTTTTTTTTTCTT	26263
rs766164185	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905932	TTCACTAAAATCACT[C/T]TTCTACTGTAATGAT	26263
rs766184353	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75928348	AGACATGGAATCAAC[C/T]TGAATGCCCATCAGT	26263
rs766200987	in-del	-/TCAT			intron-variant	FBXO22	GRCh38.p7	15:75913030	TTATTTGCCCAGTAG[-/TCAT]TCATTCAGTAGCAGG	26263
rs766216225	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75906906	AATTATAGACTGCAA[A/G]TGCATTAATGACAAG	26263
rs766218533	snp	C/T	1.72653e-05	0.00293809	intron-variant	FBXO22	GRCh38.p7	15:75913155	GACTATGCAGAAGCA[C/T]TGATGGATTCATGGG	26263
rs766277062	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929913	CCTGAACTTCGTGTG[A/G]TCCTTGTCTTTGGTT	26263
rs766277627	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75914615	TGGTACCACTCTTCA[A/G]TGTTTACAGCATGAG	26263
rs766349889	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75914616	GGTACCACTCTTCAA[G/T]GTTTACAGCATGAGG	26263
rs766455332	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929756	TAAAAAATGGAAAAT[G/T]TGATAGCTTAAGCCA	26263
rs766497168	snp	A/G/T	3.29478e-05	0.00405867	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932848	CCAGAGCATAACACC[A/G/T]TTGGCTTCATGTTTG	26263
rs766519487	snp	A/G	1.65231e-05	0.00287424	intron-variant	FBXO22	GRCh38.p7	15:75904640	TTGAGGCAAGTAGCA[A/G]GGGGTGTCATGCACA	26263
rs766657640	snp	C/T	0.000115303	0.00759199	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932949	TTTTCCTAGTGTTCC[C/T]TTATTCGGCTTCTTT	26263
rs766788609	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75920168	GCTTATGTGATTTTG[-/T]AATAACATAATGAGA	26263
rs766823327	snp	C/G	1.64972e-05	0.00287199	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917257	GATCAGGTAGCAATC[C/G]ACCTCAGGAAATAGA	26263
rs766884986	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75913628	ATGAGGTCCCATTTA[-/C]CTAAAGTTATGTAGA	26263
rs767005225	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75921626	AGATTACACCACTGC[A/C]CTCCAGCCTGGGCGA	26263
rs767033773	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920467	AAGAAGATGATCAAT[A/G]TGTTGATGTTGACGA	26263
rs767046903	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915113	GCTGGGATCACAGGC[A/G]CCCGCCACCACCACA	26263
rs767077682	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906025	ATATCTGTACACTCT[C/T]GGAGTCTTATTTAAT	26263
rs767105229	snp	A/C	8.28466e-05	0.00643556	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917309	TTTATTATTCCCTCA[A/C]ATTGAAGGAATAAAA	26263
rs767170519	in-del	-/T	0.0252718	0.109532	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933726	CTTTCCTTAAAAATA[-/T]TTTTTTTTCACCTAG	26263
rs767178887	in-del	-/AAAAAC			intron-variant	FBXO22	GRCh38.p7	15:75921792	TTTAAGCTTTTTGTT[-/AAAAAC]TAAAACACAGTCACA	26263
rs767361655	snp	A/C	1.64727e-05	0.00286986	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932939	TTAGAAAGTTTTTTC[A/C]TAGTGTTCCCTTATT	26263
rs767429345	snp	C/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930170	AGATAATAGTTCATT[C/T]CATTTTGTAGTAGAC	26263
rs767689897	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902904	TAGGTGGGGACAAAC[C/T]TGTGTCTGCTGTGCT	26263
rs767734631	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75923910	GGGCTGAATGGACAG[G/T]ATGTGGTGACTGATG	26263
rs767755524	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75924880	CCTCCCTCTCTTTTC[C/T]TTTTACAAATATCCT	26263
rs767955972	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75926204	CAGATTCTATGGCGG[A/G]TGGCCCAGAACATTG	26263
rs768082313	snp	C/T	1.64871e-05	0.00287111	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914155	TTGCCCTTGAGAAGC[C/T]ATTCCCCAAACAATG	26263
rs768121710	snp	C/T	1.64749e-05	0.00287005	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904577	CAGGCCTGGCGGAGG[C/T]CGGCCACCTGGAGGG	26263
rs768280681	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933013	ACTGGGAACTTTATA[C/T]TGAGGAAATGTAATG	26263
rs768299277	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75910845	TCTTTGCCCATGCCT[A/G]TGTCCTGAATGGTAT	26263
rs768347686	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924361	GGATCTCCTTGAGCC[A/G]TTTCTTAGCTTTTGT	26263
rs768561454	in-del	-/AAG			intron-variant	FBXO22	GRCh38.p7	15:75907266	TCTCCATAAAATAAA[-/AAG]AAAAATAATAATTTT	26263
rs768586180	snp	A/C			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	FBXO22, NRG4	GRCh38.p7	15:75935142	TCCTCCCTGCCTCTC[A/C]GAGGCCCTGAAGTCC	26263
rs768901342	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75913645	TAAAGTTATGTAGAG[A/G]AATGGTGCATTTTTG	26263
rs768906416	in-del	-/CT	1.64792e-05	0.00287042	frameshift-variant, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929904	TTAGATAACCCTGAA[-/CT]TCGTGTGGTCCTTGT	26263
rs768934072	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906566	AAGGGAAACCTGGTT[C/T]TCATCATTCTTAATG	26263
rs768954612	snp	G/T	1.65274e-05	0.00287462	intron-variant	FBXO22	GRCh38.p7	15:75917215	ATTGGTGAAACTGTT[G/T]AACTTTTTCTCTAGT	26263
rs768972428	snp	A/T	1.79232e-05	0.00299354	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932669	TGAGATATTGCCACT[A/T]TTCTAAATTTTCCAG	26263
rs768987380	snp	A/C/G	0.000319773	0.0126411	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904016	CCTCCGTAGACCCGC[A/C/G]GAGCACCTTCGTGTT	26263
rs769045298	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932787	GGACGTCAGTGATGA[A/G]AAGACTGCTGAGGCT	26263
rs769093846	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915272	ACTGCACCTGGCTGC[C/T]GTTATGTTTTTTTGT	26263
rs769114193	snp	C/T	4.2407e-05	0.00460453	intron-variant	FBXO22	GRCh38.p7	15:75904124	GAGAGGAGGCGGAGG[C/T]GGGAAGCTTGCCTGG	26263
rs769183879	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75916531	TTTAATCTTAACTAT[C/G]TCTTTAAAGGCCTTA	26263
rs769393740	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75926295	GGCATTGCTCCTTAT[G/T]CTTCCCTCATATTTT	26263
rs769393904	snp	A/G	3.29468e-05	0.00405861	intron-variant	FBXO22	GRCh38.p7	15:75904449	GTGGGAGAGACGAAA[A/G]TGAACGTCCGTTCGC	26263
rs769395763	snp	C/G/T	3.29453e-05	0.00405854	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932916	GGGGAATGTTGAGGC[C/G/T]GATGCATTTAGAAAG	26263
rs769405706	in-del	-/CTGA			intron-variant	FBXO22	GRCh38.p7	15:75904350	TTCCGAACTAGCGCC[-/CTGA]CTGACACCTACCTAC	26263
rs769452909	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75929010	GCTGTAACAAAGTAC[C/G]CCAAATTTGGTGACA	26263
rs769486004	snp	C/T	9.88468e-05	0.00702948	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932822	TGCAGCGCCTCAAAG[C/T]GGCCAACATTCCAGA	26263
rs769518649	snp	G/T	3.29468e-05	0.00405861	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904554	TCGGAGCGTAACCTG[G/T]ATCTCCGCAGGCCTG	26263
rs769550850	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934390	CAAGAGAGAAATTAG[A/C]ATATTCCATCTAATA	26263
rs769695334	snp	C/G	1.65078e-05	0.00287291	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914122	CAGCAAGGAAAAGAA[C/G]TAGTATGGAAACAGC	26263
rs769791637	in-del	-/AAA			intron-variant	FBXO22	GRCh38.p7	15:75916058	AGACTCTGTCTCCAA[-/AAA]AAAAAAAAAAAAAAA	26263
rs769845453	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75929179	TGTGGTCACACTGCC[-/T]TTTCTTCTCTGTCTC	26263
rs769858288	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75929707	TGGAAAACTTGATAC[A/G]GAGATCGAAGAGGAT	26263
rs769871187	snp	A/C/T	0.000127836	0.00799386	missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904011	CGGCTCCTCCGTAGA[A/C/T]CCGCGGAGCACCTTC	26263
rs770114550	snp	G/T	1.6489e-05	0.00287128	missense, intron-variant	FBXO22	GRCh38.p7	15:75930059	TGAAAAGTATGTCTT[G/T]TGTGCTTCTGATTTC	26263
rs770190016	snp	A/C			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902997	AGATTGCTGGGCCTC[A/C]CCCCCAGTGTCTGAT	26263
rs770222849	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902459	ATCTCAACGCTTTGG[C/G]AGGCGGAGGCAGAGG	26263
rs770237215	snp	C/T	3.6152e-05	0.00425143	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932662	TGTTTCATGAGATAT[C/T]GCCACTTTTCTAAAT	26263
rs770240936	snp	A/G	1.67307e-05	0.00289224	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903956	TGGTTCCGGCGGGCT[A/G]GTGAGGAATGGAGCC	26263
rs770262012	in-del	-/GGA			intron-variant	FBXO22	GRCh38.p7	15:75918428	AATAATGTGGAAGAG[-/GGA]GGTGGTCAGGTCAAA	26263
rs770310664	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903558	CCCTGGAGTTTCAGA[C/G]CAGCCTGGAAACCCG	26263
rs770473372	in-del	-/TTTA	4.94352e-05	0.00497143	frameshift-variant, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933006	ATAGTCACTGGGAAC[-/TTTA]TTTATATTGAGGAAA	26263
rs770522093	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915137	CACCACACCTGGCTA[A/G]TTTTTGTATTTTTAG	26263
rs770571127	snp	A/T			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935726	TGCAACTGGTTTATA[A/T]TGCAAATTTAACAAA	26263
rs770647328	snp	A/G	6.58946e-05	0.0057396	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932805	GACTGCTGAGGCTGC[A/G]ATGCAGCGCCTCAAA	26263
rs770680782	snp	G/T	1.65778e-05	0.002879	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913255	CTGATTCAGAAACTT[G/T]CATTAGTCTGGAAGA	26263
rs770735341	snp	A/C	1.70177e-05	0.00291694	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932698	AGGAACCCTCTGGAT[A/C]TTGATGCCTCGGGTG	26263
rs770774348	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922798	TGAGGACTAGGGAAT[A/G]AATTGGAGGAAATGA	26263
rs770876640	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75909940	CTCCCTGACAGGCCC[G/T]GGTGTGTGATGTTCC	26263
rs770889567	snp	G/T	0.000217202	0.0104189	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903941	GAGCCGCCGTAGGAC[G/T]GGTTCCGGCGGGCTG	26263
rs770981757	snp	C/T	4.94376e-05	0.00497156	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75930027	GGCCAGGTGGACAAC[C/T]TGTCATCACTGACTT	26263
rs770989647	snp	A/G	1.65847e-05	0.0028796	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933070	AGCTATACAACAATA[A/G]TGGCACTCATACATC	26263
rs771205426	snp	A/C			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931312	TTCACATGACCCATT[A/C]ATTTTAATGTGGTCT	26263
rs771212910	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75918546	TATGTTGAAGAGATA[C/T]CTGCACTCCCATGTT	26263
rs771249311	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75909135	TTCAGCTGCTTTGCC[A/G]CTTGTCTTCAATTGG	26263
rs771372323	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903635	TGTAGTTAAAGCTAC[A/G]AGGGAGGCTGAGGCG	26263
rs771411227	snp	G/T	0.000131922	0.00812058	intron-variant	FBXO22	GRCh38.p7	15:75917404	AAGTAGGTAAGTTAC[G/T]TTTATTTATCATTAA	26263
rs771426136	in-del	-/TACAG			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931159	AATGGTGATTCAACA[-/TACAG]TACAGTTTACCTTTG	26263
rs771468580	in-del	-/ATATAC			intron-variant	FBXO22	GRCh38.p7	15:75906409	TGTATATACATTAGT[-/ATATAC]ATATACACACATTTA	26263
rs771677073	snp	C/T	1.6631e-05	0.00288362	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913230	TTACCACATACAGTT[C/T]TTTACATGGCTGATT	26263
rs771692781	in-del	-/TTT			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930510	GTTTGGTCACAAAAC[-/TTT]TTTTTTCCACAGAAT	26263
rs771742217	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902237	TCCATGTTCGTAAGA[C/T]GCCAGTGAGCTTTCT	26263
rs771825258	snp	C/G	3.29973e-05	0.00406172	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933048	AAAAGATGATGATCT[C/G]TTTCATAGCTATACA	26263
rs771856550	snp	A/G	1.66092e-05	0.00288172	intron-variant	FBXO22	GRCh38.p7	15:75904673	CATTTGCAGGTTGGT[A/G]GTTCAGTCTTTGAGA	26263
rs771902897	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75910623	TGGGGTTGTTTTTTT[C/G]TTCAAATTTATTTAA	26263
rs771971490	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75912698	AGTCTATTTTGTTAA[-/T]TCTTTTCAAAAAACC	26263
rs771996586	snp	C/T	0.000133467	0.00816796	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903915	CTATGCTGGCGTAAT[C/T]GGGTTCCTCCGAGCC	26263
rs772011588	snp	C/T	0.000106001	0.00727939	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917386	AAAGACATCAACTCA[C/T]TGAAGTAGGTAAGTT	26263
rs772069049	in-del	-/GTTTTTAAAAAGTTTTCTATG			intron-variant	FBXO22	GRCh38.p7	15:75907050	TTTTTTCCATTTACT[-/GTTTTTAAAAAGTTTTCTATG]GTTTTTAAAAAGTTT	26263
rs772384272	snp	A/G	1.64741e-05	0.00286998	intron-variant	FBXO22	GRCh38.p7	15:75904442	GTGAGCTGTGGGAGA[A/G]ACGAAAATGAACGTC	26263
rs772459909	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904542	ATTGCGGACCCATCG[A/G]AGCGTAACCTGGATC	26263
rs772485116	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75913873	TCACTGGGGCAAAAG[C/T]AATATATGAACAGAG	26263
rs772667850	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75929149	TTCTCTTCCTACCGC[C/T]CCAGTTTCTGCTTCT	26263
rs772837985	snp	A/T	0.000151183	0.00869302	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903968	GCTGGTGAGGAATGG[A/T]GCCGGTAGGCTGCTG	26263
rs772888237	in-del	-/GT	1.6473e-05	0.00286988	frameshift-variant, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904512	CCGCTTATGGAGGGA[-/GT]GTGTGCGCAGAGTAT	26263
rs772908326	snp	C/T	0.000107469	0.0073296	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932670	GAGATATTGCCACTT[C/T]TCTAAATTTTCCAGG	26263
rs772920950	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920144	GGAGCAAATGTGGCT[A/G]TGTGCTGAGCTTATG	26263
rs772922581	snp	C/T			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935456	TTCATCTACATACTT[C/T]CAAAGCAAAATAATT	26263
rs772960050	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929086	GAAATTGAGATGGCA[G/T]TAGGGGTAGTGCTAC	26263
rs773008819	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75921315	GCCTAGCCCTGTATA[C/T]TACTATATAGTTTAT	26263
rs773066896	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906804	AATTCAAAATGCAAG[C/T]AGATTTCCTCGAAAG	26263
rs773118952	snp	C/T	1.65963e-05	0.0028806	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913244	TCTTTACATGGCTGA[C/T]TCAGAAACTTTCATT	26263
rs773149520	snp	A/G	8.30503e-05	0.00644346	intron-variant	FBXO22	GRCh38.p7	15:75904674	ATTTGCAGGTTGGTG[A/G]TTCAGTCTTTGAGAA	26263
rs773299366	snp	A/C	1.79638e-05	0.00299693	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917389	GACATCAACTCACTG[A/C]AGTAGGTAAGTTACT	26263
rs773370197	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929719	TACAGAGATCGAAGA[G/T]GATATAAAATAAGAT	26263
rs773405572	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932941	AGAAAGTTTTTTCCT[A/G]GTGTTCCCTTATTCG	26263
rs773447754	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75916722	TAATGGCTATATTCT[A/G]TGATACCAATGTAAC	26263
rs773568083	snp	A/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917251	CAATGGGATCAGGTA[A/G]CAATCGACCTCAGGA	26263
rs773774511	snp	C/T	1.6571e-05	0.0028784	intron-variant	FBXO22	GRCh38.p7	15:75904664	ATGCACAGTCATTTG[C/T]AGGTTGGTGGTTCAG	26263
rs773806650	in-del	-/GAT	3.29764e-05	0.00406043	cds-indel, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933037	TGTAATGAGGTAAAA[-/GAT]GATGATCTGTTTCAT	26263
rs773901647	in-del	-/TAAT	3.43109e-05	0.00414177	utr-variant-3-prime, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933103	GGGTCATCTAAATAA[-/TAAT]TAAAGTGGCTTTCAT	26263
rs773972060	snp	G/T	1.64879e-05	0.00287118	intron-variant	FBXO22	GRCh38.p7	15:75929865	CTGTCTTTAACTGTT[G/T]CTCTTCATTTCTCTG	26263
rs774042866	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75921538	CATAGTGGTGTGCGC[A/C]TGTAGTCCCAGCTAC	26263
rs774126509	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75907042	GTTAGCTTTTTTTTC[C/T]ATTTACTGTTTTTAA	26263
rs774335782	snp	A/C	1.6477e-05	0.00287024	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904584	GGCGGAGGCCGGCCA[A/C]CTGGAGGGGCATTGC	26263
rs774350053	snp	A/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932933	ATGCATTTAGAAAGT[A/T]TTTTCCTAGTGTTCC	26263
rs774474212	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75918623	TGTCCATTAGCTGAT[C/G]GTGGATAAAGAAAAT	26263
rs774606617	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75926978	ACAGACCTAGAGTTA[A/C]AATTGACATGTCCTT	26263
rs774761111	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75906766	ACTCTTCCCATTTTC[-/T]CCAGAAGTTTATCAT	26263
rs774885495	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75923191	TCAGTTTATAAGAGC[C/T]AAAATCTTGAGCAGC	26263
rs774975190	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75926384	CGGTAGCACCAGGTA[G/T]TCTGTTGGTTAAATA	26263
rs775067681	in-del	-/TA			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902403	CGCCTATAAATAGAC[-/TA]TGGGAAAAAACTGGC	26263
rs775096776	snp	A/G	1.64735e-05	0.00286993	intron-variant	FBXO22	GRCh38.p7	15:75904455	GAGACGAAAATGAAC[A/G]TCCGTTCGCAATCCT	26263
rs775257110	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924344	TTGAGACTACTCAGT[A/G]AGGATCTCCTTGAGC	26263
rs775351700	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75910676	TAGCCCTTTGTCAGA[A/T]GGATAGGTTGCAAAA	26263
rs775458719	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75931514	TTTTAAGAGCAGCAG[A/T]GGACTTCAGAAGACG	26263
rs775629790	in-del	-/AAAA			intron-variant	FBXO22	GRCh38.p7	15:75916057	AAGACTCTGTCTCCA[-/AAAA]AAAAAAAAAAAAAAA	26263
rs775633428	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75921991	TGTTTTACAGTTAAC[-/T]TTTTTTTTTTTTTTA	26263
rs775652715	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75926581	TGGAGAAGATGGTGT[C/T]AACTGGAATGTGTGA	26263
rs775706307	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75918748	AAGCCAGGCCCAGAA[A/G]GACAAATAGTGCATG	26263
rs775722788	snp	C/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903903	GGCCGGGCAACCCTA[C/T]GCTGGCGTAATCGGG	26263
rs775736485	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75912348	CAGAAGGAATGGTAT[A/T]AGTTCCTCTTTGTAC	26263
rs775794407	snp	C/T	1.64879e-05	0.00287118	missense, intron-variant	FBXO22	GRCh38.p7	15:75930060	GAAAAGTATGTCTTG[C/T]GTGCTTCTGATTTCG	26263
rs775992880	snp	C/T	0.000976172	0.0220711	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903958	GTTCCGGCGGGCTGG[C/T]GAGGAATGGAGCCGG	26263
rs776028665	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75910863	TCCTGAATGGTATTG[C/T]CTAGATGTTCTTCTA	26263
rs776103816	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75913973	TGTTTGTTTTAATCA[A/G]TGCTTTTAGACCTTT	26263
rs776151270	snp	A/G	6.90822e-05	0.00587676	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904032	GAGCACCTTCGTGTT[A/G]AGTAACCTGGCGGAG	26263
rs776213418	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924534	AGGCATCTTTGGAAC[A/G]CTTTGCCCACCAAAG	26263
rs776299673	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75926081	TCACCAGTAGGTTAC[A/G]CTGTTTAAAGTGCCT	26263
rs776321484	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934296	TAGAAGAAAAACAAC[A/C]GAAGGATCCTGGTCC	26263
rs776366380	snp	A/G	1.65759e-05	0.00287883	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913257	GATTCAGAAACTTTC[A/G]TTAGTCTGGAAGAGT	26263
rs776379999	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75921718	GCTAGACAAAAAAAA[A/T]TTCCATTTATATCCT	26263
rs776423393	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932813	AGGCTGCGATGCAGC[A/G]CCTCAAAGCGGCCAA	26263
rs776429552	snp	A/G			missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933067	CATAGCTATACAACA[A/G]TAATGGCACTCATAC	26263
rs776482925	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919818	GAGGAGCATACATGT[A/G]TCTGGGCTTGAAGTG	26263
rs776809573	snp	C/G	0.00010518	0.00725114	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903946	GCCGTAGGACTGGTT[C/G]CGGCGGGCTGGTGAG	26263
rs776811831	snp	G/T	1.72519e-05	0.00293695	intron-variant	FBXO22	GRCh38.p7	15:75913156	ACTATGCAGAAGCAC[G/T]GATGGATTCATGGGA	26263
rs776866817	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906592	TAATGTATTTAGATA[C/T]TACATCAATGCCCCA	26263
rs776896256	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75928099	AAAAGTCAAAAAATA[A/G]CAGATGCTGGCAAGT	26263
rs776925520	in-del	-/T	3.59147e-05	0.00423746	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932668	ATGAGATATTGCCAC[-/T]TTTCTAAATTTTCCA	26263
rs776975292	snp	C/G	1.66771e-05	0.00288761	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933078	AACAATAATGGCACT[C/G]ATACATCTGGGGTCA	26263
rs777002700	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75915352	AAAGATTTTTGATCT[G/T]AATTTGAGTCTTATA	26263
rs777108746	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75930042	CTGTCATCACTGACT[C/T]CTGAAAAGTATGTCT	26263
rs777148157	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75927662	AAAGATGCTTTAGCA[A/G]TGGTTTGGGGTATAT	26263
rs777301151	snp	A/G	1.6869e-05	0.00290417	intron-variant	FBXO22	GRCh38.p7	15:75914074	ATTTGACTTTAAATG[A/G]ATGATATTTATCATT	26263
rs777426049	snp	A/C	3.32077e-05	0.00407465	intron-variant	FBXO22	GRCh38.p7	15:75914209	CAGGAATTGTAGGTG[A/C]GATAAATTAGCAACT	26263
rs777442970	snp	A/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932313	ATGTAAACAATAGCA[A/G]AAGGCTTCGTTTAGT	26263
rs777670350	in-del	-/T	3.38438e-05	0.00411349	intron-variant	FBXO22	GRCh38.p7	15:75914066	ATTCTCAGATTTGAC[-/T]TTAAATGGATGATAT	26263
rs777717844	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75909697	ATGAGTGAAAAGTAA[A/G]TGAGAAGTAGATTGA	26263
rs777731927	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922782	AAATAACACTAGGGC[A/G]TGAGGACTAGGGAAT	26263
rs777755878	snp	G/T	0.000448589	0.0149697	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903998	GCGGCGAGTGCCGCG[G/T]CTCCTCCGTAGACCC	26263
rs777757312	in-del	-/GGAAGTGG			intron-variant	FBXO22	GRCh38.p7	15:75914849	CACTGTCCTCATCAA[-/GGAAGTGG]GGAAGTGGGGATGAT	26263
rs777809909	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920501	GACTATCTATATTCA[A/G]TTGGCTCATAATGTA	26263
rs777819796	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923948	AGGTGTTGAGAATGA[A/G]GGAGGTGACAGCGAT	26263
rs777867295	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929995	CTTTCAGTGATATGA[A/G]TATCATCTTGGCTGG	26263
rs777913952	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75923668	CAAGAGTGGATGCAG[C/G]ATTAGCTTGATTTAG	26263
rs777956370	in-del	-/TT			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934663	AAGTCCAAAGAAAAA[-/TT]TGTCAAAACTTTTCA	26263
rs778001561	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75911388	ATATCGATTCTTCCT[A/G]TCCTTGAGCATGGAA	26263
rs778035636	snp	A/C/T	3.29464e-05	0.00405861	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904551	CCATCGGAGCGTAAC[A/C/T]TGGATCTCCGCAGGC	26263
rs778050786	snp	A/C	1.82527e-05	0.00302093	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932639	GCTTCTATACTTAAA[A/C]ATTTTAATGTTTCAT	26263
rs778136849	snp	C/T	0.000129509	0.00804596	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903925	GTAATCGGGTTCCTC[C/T]GAGCCGCCGTAGGAC	26263
rs778139962	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75921641	CTCCAGCCTGGGCGA[-/C]CAGCGAGACTCTATC	26263
rs778191823	snp	A/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932333	CTTCGTTTAGTGGAT[A/G]TCTTTGTGTATATTA	26263
rs778218110	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75918215	GACTTAAACCAGCTG[A/G]AGTAAAAAATTGTGT	26263
rs778272876	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915222	GTGATCCACCGCCTC[A/G]GCCTCCCAAAGTGCT	26263
rs778391406	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75917927	AAACATCCTGCAGGT[A/T]GTGTGGATGGAGCCC	26263
rs778552849	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903335	GGACTACGAAGAGCA[A/G]TAAGTACTACCTAGT	26263
rs778651491	snp	A/G	3.32906e-05	0.00407973	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913226	CATCTTACCACATAC[A/G]GTTCTTTACATGGCT	26263
rs778693759	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924103	GAGATATTGATTATA[A/G]ACAGTTGGATATGTT	26263
rs778706225	snp	A/G	3.29614e-05	0.00405951	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933018	GAACTTTATATTGAG[A/G]AAATGTAATGAGGTA	26263
rs778773523	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75904354	GAACTAGCGCCCTGA[C/T]TGACACCTACCTACC	26263
rs778781219	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75909941	TCCCTGACAGGCCCT[A/G]GTGTGTGATGTTCCC	26263
rs778889231	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929978	GCAGCAAGTAGTCAG[C/T]ACTTTCAGTGATATG	26263
rs779150555	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920708	CGCACCTGTAGTCCC[A/G]GCTACTTAGGAGGCT	26263
rs779152280	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75912544	TCTTCTAGATTTTCT[A/T]GTTTATTTGCATAGA	26263
rs779275797	snp	A/G	6.83165e-05	0.00584411	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917369	AAAGAATTTAACATT[A/G]GAAAGACATCAACTC	26263
rs779299583	snp	C/T	2.20968e-05	0.00332384	intron-variant	FBXO22	GRCh38.p7	15:75904136	AGGCGGGAAGCTTGC[C/T]TGGGGACACGCCGTG	26263
rs779321020	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919530	GGCTCTCCAGTTAGG[A/G]CAAGTTTTTCAATTT	26263
rs779339421	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75904388	GGGACTTTGGATCCC[G/T]CAGGGATCTCCTGCT	26263
rs779408236	snp	G/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934789	AAATATTTTTTAAAC[G/T]TTATTGTCCCTGATA	26263
rs779526889	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75904300	TCCCTGAGGGGCGAA[A/G]TTCCCCTTAAGGTTT	26263
rs779547751	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908434	CATGCAGCCATACCC[A/G]GTTACTTTTTGTATT	26263
rs779569723	snp	A/G	0.000219034	0.0104627	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933767	CTAACTAACTGGTAG[A/G]CCAGAGTATTACATC	26263
rs779624559	snp	A/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903423	AGGGCAGTGAGAGGC[A/T]CAGGCACAGAAGAAG	26263
rs779656571	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905079	CCGCCCGCCTCGGCC[C/T]CCCAAAGTGCTGGGA	26263
rs779707516	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75925928	AAGAACAGTTTCATC[C/T]TATTCCAAAACCAAA	26263
rs779728021	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75911797	CAGAACCTCCAATAC[C/T]ATGTTGAATAGGAAT	26263
rs779772186	snp	C/T	1.64789e-05	0.0028704	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933011	TCACTGGGAACTTTA[C/T]ATTGAGGAAATGTAA	26263
rs779807387	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75924411	CAGTCTTACATGGGA[A/T]GTCAACATAAAAATA	26263
rs779878931	snp	C/T	1.66916e-05	0.00288886	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917333	AATAAAAATACAACC[C/T]TTTCATTTTATTAAG	26263
rs779940061	snp	A/T	1.66092e-05	0.00288172	intron-variant	FBXO22	GRCh38.p7	15:75917181	CCTAAACTGTAGTTA[A/T]CTAGTTTTTACTGAC	26263
rs779978537	snp	G/T	0	0	intron-variant	FBXO22	GRCh38.p7	15:75911079	agatcgttgtagatg[G/T]gtggtgttatttctg	26263
rs780018144	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934949	TCAAAGAGTCTGATA[C/T]AGGGTAATTTCATAC	26263
rs780157276	snp	C/T	3.60458e-05	0.00424518	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904077	GCTCACCTTCCTGCC[C/T]GCCAAGGCGTTGCTG	26263
rs780255988	in-del	-/TTCCC	6.60677e-05	0.00574713	intron-variant	FBXO22	GRCh38.p7	15:75929835	GCATGTATAAAATAA[-/TTCCC]TTTCTGTTTTAAGGC	26263
rs780268475	in-del	-/AC			intron-variant	FBXO22	GRCh38.p7	15:75916616	AGTAGGGAGGGAATG[-/AC]ACACAGTTCAATCTG	26263
rs780286954	snp	G/T	6.58903e-05	0.00573941	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904520	GGAGGGAGTGTGTGC[G/T]CAGAGTATTGCGGAC	26263
rs780463125	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75920814	GGTGACAGAGTGAGA[A/C]CCTGTCTCAAAAATA	26263
rs780538180	snp	A/G	3.29538e-05	0.00405904	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932770	ACTGTGCTCCTCAAC[A/G]AGGACGTCAGTGATG	26263
rs780551036	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75922196	GACATTTGAGTAATG[C/T]GTTGTGCTACACATT	26263
rs780553089	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75906383	TAAGTATGTATATAC[A/T]TGCATGTGTATGTAT	26263
rs780571661	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907849	TTGGGTAGCTGAGGT[A/G]CCAGAATCGCTTGAA	26263
rs780978052	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932913	CAAGGGGAATGTTGA[A/G]GCTGATGCATTTAGA	26263
rs780984979	snp	C/T	1.67315e-05	0.00289231	intron-variant	FBXO22	GRCh38.p7	15:75914228	AAATTAGCAACTTGA[C/T]GATTTCTTCCTTGCA	26263
rs781120566	snp	C/T	1.6676e-05	0.00288751	intron-variant	FBXO22	GRCh38.p7	15:75914093	ATATTTATCATTTTG[C/T]TACTGTATTTTTACA	26263
rs781125179	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75913631	GAGGTCCCATTTACT[A/G]AAGTTATGTAGAGAA	26263
rs781134098	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75916250	ACAATTTTCTGTAGA[C/T]TTGTAACCTACTGTG	26263
rs781135442	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75915021	CACCAAGGTTGGAGT[G/T]CAATGGCGTGATCTC	26263
rs781228122	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75931754	TGTAAGGATATTTCA[-/T]TTTTTTAAAAAAACC	26263
rs781235403	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	FBXO22, NRG4	GRCh38.p7	15:75935165	TGAAGTCCTGTGAGG[A/G]AGGGAAATAGTAATT	26263
rs781275509	in-del	-/AA			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933187	ATGTGTATTTCAAAC[-/AA]AAATAACTTTAGATA	26263
rs781291730	snp	A/G	1.82337e-05	0.00301936	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932646	TACTTAAAAATTTTA[A/G]TGTTTCATGAGATAT	26263
rs781326060	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75921043	ATGTTACAGCCTACT[A/G]TATGTGTAGGCTATA	26263
rs781411973	snp	C/T	1.76799e-05	0.00297315	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904065	GGTGGAGCGTGTGCT[C/T]ACCTTCCTGCCCGCC	26263
rs781416721	snp	C/T	1.648e-05	0.0028705	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932764	AGTGCCACTGTGCTC[C/T]TCAACGAGGACGTCA	26263
rs781602044	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75909486	GTGAAAAGGGAGTGA[C/T]ACAGCCTGTATACCT	26263
rs781725457	snp	A/G	1.66918e-05	0.00288888	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913212	TTGCAGAATGTTCGC[A/G]TCTTACCACATACAG	26263
rs781757824	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920282	TAGGTCTGAAACTCA[A/G]AGGAATGGCTGTGGT	26263
rs796388861	in-del	-/TT			intron-variant	FBXO22	GRCh38.p7	15:75916865	TTTTAGGGTAAACTT[-/TT]AAAAATTGGAATTGC	26263
rs796395084	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75909649	AATGAAGAAATTATA[C/G]GTGTTTAGTAAATGA	26263
rs796439307	in-del	-/GTAGCTC			intron-variant	FBXO22	GRCh38.p7	15:75908663	GCTGAAGAGGGTCAG[-/GTAGCTC]AATAGTCGTAGCACC	26263
rs796530032	in-del	AA/G			intron-variant	FBXO22	GRCh38.p7	15:75915466	ATTTTTTTAAAAAAA[AA/G]AGTTTATTTCTTTTT	26263
rs796679054	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75915452	CTAAAGGGCTTAACA[-/T]TTTTTTTAAAAAAAA	26263

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