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

RNF113B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs510858	snp	C/G/T	3.30038e-05	0.00406212	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176918	CGGTGGCCCCCATGT[C/G/T]CTCTGGCCCCACAGG	140432
rs515170	snp	C/T	0.376195	0.215812	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177375	ACAAGAGTGAGTCAC[C/T]GCGCCTGGCCTAGCA	140432
rs626950	snp	C/T	0.375996	0.215928	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177364	TCACCGCGCCTGGCC[C/T]AGCAGAAGCTTTTCT	140432
rs628778	snp	A/G	0.20236	0.245424	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176922	GAAGCCTGTGGGGCC[A/G]GAGGACATGGGGGCC	140432
rs774690	snp	A/T	0.374	0.217081	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176006	CCATGTTCACTGCAG[A/T]ATTATTTGCAAAAGC	140432
rs1853333	snp	A/G	0.203267	0.245593	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179214	cgcatggcagcagac[A/G]agaacagaatgagaa	140432
rs5806050	in-del	-/A	0.290718	0.246662	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175523	TTTTGAAAAAAAAAA[-/A]TTAATTATAGTACAA	140432
rs5806051	in-del	-/AA	0.499234	0.0195537	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177485	AACTCCATCCTTACT[-/AA]AAATACAAAAATTAC	140432
rs9517208	snp	A/G	0.481473	0.0944461	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178689	ATTCAGCTCACTTGT[A/G]GTGCCCCCAAAACAC	140432
rs9556890	snp	C/T	0.241914	0.249869	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178022	ATTAAAAGACTGTCA[C/T]ATCACACTGCACCTG	140432
rs9556891	snp	A/G	0.0667028	0.170006	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178459	CCTTGGCCTCCTAAA[A/G]TGTTGGTATTACAGG	140432
rs9556892	snp	C/G	0.330016	0.236849	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179097	ctgataaagacacac[C/G]tgagactgggtaatt	140432
rs12868132	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177761	TCACTTGCTCCTCAG[C/T]TCCCTCAGTGCACAC	140432
rs16955011	snp	C/T	0.13988	0.224441	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176963	TGGACCTGTACACCA[C/T]GTCGAGGCTCTCAGG	140432
rs34253287	snp	C/G	0.0174215	0.091708	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177012	CCTGTCGCCGTGAGC[C/G]GCCTTCTGCCAGCTG	140432
rs41300600	snp	C/T	0.0105365	0.0718137	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176638	CAGAAGCCAGTCTCC[C/T]TGTAGTCCTTGCAGA	140432
rs56197828	in-del	-/AA	0.499343	0.0278555	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179213	CGCATGGCAGCAGAC[-/AA]GAGAACAGAATGAGA	140432
rs57310501	in-del	-/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178213	TTTTTTTTTTTTTTT[-/T]GAGAAAGAGTCTCGC	140432
rs58126526	in-del	-/A	0.498323	0.0289051	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177667	AAAAAAAAAAAAACC[-/A]AAAAAAAAAGGCTTC	140432
rs61968647	snp	A/G	0.00636936	0.0560724	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175301	TTTGTCTTGGGAGAG[A/G]AATACATTGCCATTT	140432
rs61998176	snp	C/T	0.0259695	0.110952	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176633	AGCCACAGAAGCCAG[C/T]CTCCTTGTAGTCCTT	140432
rs67801656	in-del	-/AA			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179214	GCATGGCAGCAGACG[-/AA]AGAACAGAATGAGAA	140432
rs71111928	in-del	-/AA	0	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178190	GCGAGACTCTTTCTC[-/AA]AAAAAAAAAAAAAAA	140432
rs72655114	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177667	AAAAAAAAAAAAACC[A/C]AAAAAAAAGGCTTCT	140432
rs73561304	snp	A/G	0.0759472	0.179459	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175689	CAGCTCCCCACTCCC[A/G]CTCTTCCTAACCCCT	140432
rs74575080	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178066	GGCTTTCATTTTGAA[A/G]TAAAAGTAACACATG	140432
rs74719265	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177652	ACCCTGTCTCAAATT[A/T]AAAAAAAAAAAACCA	140432
rs74851889	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178021	TATTAAAAGACTGTC[A/C]TATCACACTGCACCT	140432
rs77681464	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179213	TCGCATGGCAGCAGA[A/C]GAGAACAGAATGAGA	140432
rs78320598	snp	A/C	0.0341408	0.126114	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175313	GAGGAATACATTGCC[A/C]TTTTAAGGGAGAGGA	140432
rs79275419	snp	G/T	0.0260105	0.111035	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177837	AGGCCATAGCGAACC[G/T]GTGGTGCTCATCCTA	140432
rs79795199	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177788	ACACTCATTTTTCAA[A/C]AGATTCCTAAAAGGC	140432
rs111427949	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177888	CGTATTTAAAAGCAA[C/T]ACACGCGCAGTGCAG	140432
rs111520418	snp	A/G/T	1.84004e-05	0.00303313	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177101	CCCCGCTGCTGCTGC[A/G/T]CTCTCCGTGCTCGGG	140432
rs113354899	snp	C/T			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175952	ATTTTGTTTGTCCAT[C/T]CATCCATCCATGGAC	140432
rs113453013	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179202	AAAGGCATGTCTCGC[A/G]TGGCAGCAGACGAGA	140432
rs113665583	snp	C/G	0.5	0	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177214	TGGTCGGCCGTCCTT[C/G]CTGGAGAAGGTGGCG	140432
rs113954616	snp	A/G	0.5	0	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176854	CGCTGGCTGCACTTG[A/G]GGATGGTCGGCGTAT	140432
rs114102979	snp	A/G	0.00930212	0.0675613	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176675	GCTGGTAATCCCAGC[A/G]CACAGTGGCGCGCAG	140432
rs114712839	snp	C/G	0.00112795	0.0237214	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176970	GTACACCACGTCGAG[C/G]CTCTCAGGCGCCGCC	140432
rs114739965	snp	A/G	0.00116968	0.0241551	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176780	TCAGGTACCTCAGGT[A/G]GCTGTGGATTCCCCG	140432
rs115032993	snp	A/G/T	0.000708092	0.0188032	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176436	CCTGCACTTGGTGAC[A/G/T]ACTGGGTTTTGGAAG	140432
rs115127901	snp	A/G	0.0341408	0.126114	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176095	TGGGATTGCAGGAAG[A/G]CTGTCATCTCTCTCA	140432
rs115981649	snp	C/T	0.000444675	0.0149044	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176522	CATGGTTTTCGTCCT[C/T]GCAGATACAGTAGCG	140432
rs116650511	snp	C/T	0.000247315	0.0111174	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176839	AGTGCCTCCTGGACC[C/T]GCTGGCTGCACTTGA	140432
rs116765314	snp	C/T	0.00131696	0.025627	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176562	AAGCTCCCGTTCAAT[C/T]TCCCACCCGAGCTTG	140432
rs118043654	snp	C/T	0.0232847	0.105357	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179196	AAGGTGAAAGGCATG[C/T]CTCGCATGGCAGCAG	140432
rs138025858	snp	G/T	0.00014833	0.00861063	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176736	CGCCATCCCCGAGGA[G/T]GAGTTGCCCATGGAC	140432
rs138253916	snp	A/G	0.000331631	0.0128727	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176923	GCCCCCATGTCCTCT[A/G]GCCCCACAGGCTTCG	140432
rs139267423	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178289	CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT	140432
rs140282190	snp	C/T	0.000181224	0.0095173	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176674	GGCTGGTAATCCCAG[C/T]GCACAGTGGCGCGCA	140432
rs140938876	snp	G/T	8.84557e-05	0.00664981	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176986	CTCTCAGGCGCCGCC[G/T]CCTCGCCCCTCCTGT	140432
rs142469809	snp	A/G	4.94173e-05	0.00497053	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176457	GTTTTGGAAGGCCTG[A/G]CGACATATGAAACAC	140432
rs143204738	snp	C/T	0.000461551	0.0151843	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176807	CCCGGTAGATGTGGT[C/T]GTGCTCCCGACCCCG	140432
rs144481331	snp	A/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175558	GTACAAAACATAAAA[A/T]GTACCCTTAACCATT	140432
rs144854034	snp	G/T	0.00132561	0.0257108	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177134	CGCAGGCCGGGCGCT[G/T]TCTGAGGCCTGCAGC	140432
rs145228466	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178381	CTGTGTTTTTAGTAG[C/T]GACAGGGTTTCACCA	140432
rs145303380	snp	A/G	0.000329658	0.0128343	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176731	TTCCTCGCCATCCCC[A/G]AGGAGGAGTTGCCCA	140432
rs145451325	snp	C/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179041	CTTTTTTCTTGGAGA[C/G]CCCCAGATGTTGGTG	140432
rs146499288	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179130	CAAAAGAAAAAGGCT[C/T]AATGGACTTACATTT	140432
rs146586427	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177665	TTAAAAAAAAAAAAA[A/C]CAAAAAAAAAGGCTT	140432
rs147264891	snp	C/T	5.18551e-05	0.00509165	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176979	GTCGAGGCTCTCAGG[C/T]GCCGCCTCCTCGCCC	140432
rs147722072	snp	A/G	4.94173e-05	0.00497053	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176415	GCAGCTCTCGCAGAA[A/G]TAATGCCTGCACTTG	140432
rs147920690	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177207	GTCTGCTTGGTCGGC[C/T]GTCCTTCCTGGAGAA	140432
rs148267601	snp	C/G	0.000148377	0.00861198	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176813	AGATGTGGTCGTGCT[C/G]CCGACCCCGCAGTGC	140432
rs148433651	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175812	TAGTTTATTTCACTT[A/G]GCAGTGTCGTCTTCA	140432
rs149265686	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175382	GCGTGGATATTCTTC[A/T]GTCAACTCCTCCCCT	140432
rs149988576	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178303	CGGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC	140432
rs150082041	snp	C/T	0.000230635	0.0107361	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176623	CTGTCCCCGAAGCCA[C/T]AGAAGCCAGTCTCCT	140432
rs151243225	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177967	CCTCAAAGATAACCA[C/G]TGTCAACACTTTTGT	140432
rs151316967	snp	A/G	0.000153988	0.00877328	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176555	CCTCTTCAAGCTCCC[A/G]TTCAATCTCCCACCC	140432
rs181635725	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175368	AAATCCAAACTTCAG[C/T]GTGGATATTCTTCTG	140432
rs181705193	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179069	GTGTCCATATTAGTC[C/T]GTTTTCACGCTGCTG	140432
rs181779793	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178684	ATGAGATTCAGCTCA[C/T]TTGTAGTGCCCCCAA	140432
rs182388789	snp	A/G	0	0	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176043	ACATACCTCTTTGAG[A/G]TCCGGATTTCAATTC	140432
rs183106529	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177442	ACCCGAGGTCAGCAG[C/T]TTAAGACCAGCCTGG	140432
rs184244691	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178436	CCTGACCTCAGGTGA[C/T]CCACCCACCTTGGCC	140432
rs184361407	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178831	TCATTTGTCAGTTTT[C/G]TCTTAGGATAGTAAT	140432
rs185073947	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177892	TTTAAAAGCAACACA[C/T]GCGCAGTGCAGAAAA	140432
rs185765267	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175645	ACTTTTTCATTTAGC[A/C]AAACTCAAGCTCTGT	140432
rs185956021	snp	A/G	6.59554e-05	0.00574224	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176847	CTGGACCCGCTGGCT[A/G]CACTTGAGGATGGTC	140432
rs187386968	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177463	ACCAGCCTGGCCAAC[A/G]TAGCGAAACTCCATC	140432
rs188748562	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178970	TGGCTGGAATCCATC[A/G]GTATTGTTGGGCTTG	140432
rs189192783	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177313	CTGCACGTGGGGCGT[A/G]GGCCCTCCCAGTTCT	140432
rs189417568	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178492	TGAGCCACTGCACCC[C/T]GCCTTCAAATATTTT	140432
rs189535288	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177996	GTGTCTATTCTTTTA[A/G]TATAGCCTTTATTAA	140432
rs190157119	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175855	GTTGTAGCATGTGAT[C/T]CTTAAAAGGATCAGT	140432
rs191799203	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177874	AGGCGCTTGAAATGC[A/G]TATTTAAAAGCAACA	140432
rs192445596	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177336	CCAGTTCTAAAAAGC[A/G]AAAGCAAGTGAAAGA	140432
rs192788917	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178354	GTGTGTGCCACCACA[C/G]CCAGCTAACTTCTGT	140432
rs199715561	snp	A/G			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175523	CTTTTTAGCTTTTTT[A/G]AAAAAAAAAATTAAT	140432
rs199748911	snp	C/T	1.64795e-05	0.00287045	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176700	GCGCAGATGCCCTGG[C/T]GCACGTATGGGGCCC	140432
rs199754785	snp	C/T	0.00199806	0.0315443	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176381	AGCAGCGCGGGGTGG[C/T]CCGGAAGTGCTCCAG	140432
rs199776079	snp	C/G/T	0.000922061	0.0214521	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176473	CGACATATGAAACAC[C/G/T]TGAATGGTATTTCCT	140432
rs199816159	snp	A/G	0.00199792	0.0315431	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176529	TTCGTCCTCGCAGAT[A/G]CAGTAGCGACCCTCT	140432
rs199939990	snp	C/G/T	0.000148431	0.00861367	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176882	TATGGTGCTCCTTCT[C/G/T]GGTGTCCTGCTCGAA	140432
rs200541421	in-del	-/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177665	TTAAAAAAAAAAAAA[-/C]CAAAAAAAAAGGCTT	140432
rs200579942	snp	A/G	0.00199808	0.0315444	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176441	ACTTGGTGACGACTG[A/G]GTTTTGGAAGGCCTG	140432
rs200582250	snp	A/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175534	TTTTGAAAAAAAAAA[A/T]TAATTATAGTACAAA	140432
rs201183546	snp	C/T	0.000247249	0.0111159	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176345	GGTTAAAGATGCCGC[C/T]GGTTGGCTGGTCACA	140432
rs201501451	snp	G/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175522	TCTTTTTAGCTTTTT[G/T]GAAAAAAAAAATTAA	140432
rs201595398	snp	A/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175536	TTGAAAAAAAAAATT[A/T]ATTATAGTACAAAAC	140432
rs201781048	snp	C/G	0.00199792	0.0315431	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176787	CCTCAGGTAGCTGTG[C/G]ATTCCCCGGTAGATG	140432
rs201842824	snp	A/T	0.000105506	0.00726237	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177264	GGCTCCCAACGGCCG[A/T]GGCGTGCGTCACCCT	140432
rs201896291	in-del	-/AC			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179211	CTCGCATGGCAGCAG[-/AC]ACGAGAACAGAATGA	140432
rs201896846	snp	A/C	1.64893e-05	0.0028713	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176819	GGTCGTGCTCCCGAC[A/C]CCGCAGTGCCTCCTG	140432
rs202164234	snp	C/T	3.33506e-05	0.0040834	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176944	ACAGGCTTCGCCGAG[C/T]GGGTGGACCTGTACA	140432
rs267603872	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176292	CCCACCTTCTGCAGC[C/T]TGAAGCTTTTGCAGT	140432
rs267603873	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176646	AGTCTCCTTGTAGTC[C/T]TTGCAGATGTCAGGC	140432
rs368346357	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177686	AAAAAGGCTTCTCCC[C/G]CCCTTCCCTCCCTTG	140432
rs368501437	snp	C/T	0.000153988	0.00877328	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177189	GAGGAAGGTGCATAC[C/T]TGGTCTGCTTGGTCG	140432
rs368911504	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177618	CGCCACTGTACTCTA[A/G]CCTGGGTGACAGAGC	140432
rs369128203	snp	C/T	4.97376e-05	0.00498662	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176248	GGAATTGGACACTCA[C/T]GGGGGTCTTCTGTGA	140432
rs369209541	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178788	TTGGAAATGTGATGA[A/G]TAAGCTTACAGTGTA	140432
rs369474969	snp	C/T	6.58892e-05	0.00573936	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176410	AGCGCGCAGCTCTCG[C/T]AGAAATAATGCCTGC	140432
rs369514869	in-del	-/C			intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176985	GCTCTCAGGCGCCGC[-/C]TCCTCGCCCCTCCTG	140432
rs370969714	snp	A/C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175935	TTGTGTGTGTGTATC[A/C/G]CATTTTGTTTGTCCA	140432
rs371770857	snp	A/G	2.11831e-05	0.0032544	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177265	GCTCCCAACGGCCGT[A/G]GCGTGCGTCACCCTT	140432
rs371853234	snp	A/G	6.16491e-05	0.00555164	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177257	AGTCTCAGGCTCCCA[A/G]CGGCCGTGGCGTGCG	140432
rs372682418	snp	G/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177769	TCCTCAGCTCCCTCA[G/T]TGCACACTCATTTTT	140432
rs373084773	snp	A/G	0.000153988	0.00877328	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176142	GCTTCTCCCCAGTGT[A/G]CATACAGACTTGAGT	140432
rs373285066	snp	C/G	1.65825e-05	0.00287941	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176253	TGGACACTCATGGGG[C/G]TCTTCTGTGAAATGG	140432
rs373685549	snp	A/G	3.29451e-05	0.00405851	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176548	TAGCGACCCTCTTCA[A/G]GCTCCCGTTCAATCT	140432
rs373868658	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177498	CTAAAAATACAAAAA[C/T]TACCTGGGTGTGGTG	140432
rs375026425	snp	A/G	1.9541e-05	0.00312572	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177062	GTGCCACCCGCGGGG[A/G]CTGAGCCACTGTGTC	140432
rs375509298	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179103	AAGACACACCTGAGA[C/T]TGGGTAATTTACAAA	140432
rs375668710	snp	A/G	0.00609841	0.0548818	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176184	CTTTTTTCCTAAAAG[A/G]ACAAAAAAATTTATT	140432
rs376046437	snp	C/G	0.000346337	0.0131548	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176883	ATGGTGCTCCTTCTC[C/G]GTGTCCTGCTCGAAG	140432
rs376197252	snp	C/T	6.2182e-05	0.00557558	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177258	GTCTCAGGCTCCCAA[C/T]GGCCGTGGCGTGCGT	140432
rs376379120	snp	C/T	3.29451e-05	0.00405851	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176495	GTATTTCCTCTTCCT[C/T]GCTTCCCACTTCATG	140432
rs376569445	snp	A/G	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177275	GCCGTGGCGTGCGTC[A/G]CCCTTGCGTCGCCCT	140432
rs376707872	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177820	ACGGGTGGAATCATT[C/T]CAGGCCATAGCGAAC	140432
rs376932060	snp	C/T	0.000153988	0.00877328	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176244	CATGGGAATTGGACA[C/T]TCATGGGGGTCTTCT	140432
rs377323551	snp	A/G	6.59131e-05	0.0057404	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176350	AAGATGCCGCCGGTT[A/G]GCTGGTCACAGATGT	140432
rs377533060	snp	A/G	0.00874735	0.0655527	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175321	CATTGCCATTTTAAG[A/G]GAGAGGATGTTAACA	140432
rs386380365	in-del	-/AA			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179212	TCGCATGGCAGCAGA[-/AA]CGAGAACAGAATGAG	140432
rs397825947	in-del	-/A	0	0	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175533	TTTTGAAAAAAAAAA[-/A]TTAATTATAGTACAA	140432
rs529356475	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177397	CACTCTTGTAATCCC[A/G]GGACACTGGGAGGCC	140432
rs529841946	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177663	AATTAAAAAAAAAAA[A/C]ACCAAAAAAAAAGGC	140432
rs533215270	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178969	CTGGCTGGAATCCAT[C/T]GGTATTGTTGGGCTT	140432
rs534127754	in-del	-/A			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178868	TTTTCTTCAACTGTT[-/A]ATCATCCCATCTTTC	140432
rs534795799	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175461	AACCCCATCCTCTCC[A/T]CTCCCTCCCGGTCTT	140432
rs536089635	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175336	GGAGAGGATGTTAAC[A/G]TCAGCCAAACAAAAT	140432
rs536477286	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175387	GATATTCTTCTGTCA[A/C]CTCCTCCCCTCCTTG	140432
rs538109725	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179088	TTCACGCTGCTGATA[A/G]AGACACACCTGAGAC	140432
rs538170646	snp	C/T			intron-variant, stop-gained	FARP1, RNF113B	GRCh38.p7	13:98176565	CTCCCGTTCAATCTC[C/T]CACCCGAGCTTGTAA	140432
rs538246834	snp	C/G			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175809	GACTAGTTTATTTCA[C/G]TTAGCAGTGTCGTCT	140432
rs539510341	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178565	ATTCATTTATATAAT[A/G]TAAATGGATTCTAGT	140432
rs539566940	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177468	CCTGGCCAACATAGC[A/G]AAACTCCATCCTTAC	140432
rs540055745	snp	C/T	3.38702e-05	0.00411509	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176966	ACCTGTACACCACGT[C/T]GAGGCTCTCAGGCGC	140432
rs540470252	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178725	GCTGTGGGATGAGGG[A/G]GAAGTTGTGTGGGTC	140432
rs540513545	snp	A/G	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178045	TGCACCTGTGGGTGT[A/G]TAGCTGGCTTTCATT	140432
rs540567065	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179242	GAACCAAGTGAAAGG[A/G]GTTTGCCCTTATAAA	140432
rs540571514	snp	A/G	0.000128096	0.00800198	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177003	CTCGCCCCTCCTGTC[A/G]CCGTGAGCCGCCTTC	140432
rs540958770	snp	C/G			intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176374	CAGATGTAGCAGCGC[C/G]GGGTGGCCCGGAAGT	140432
rs544513726	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179249	GTGAAAGGGGTTTGC[C/T]CTTATAAAACCATCA	140432
rs544679195	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178803	ATAAGCTTACAGTGT[A/C]AAGAACAATTCATCA	140432
rs546180105	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177316	CACGTGGGGCGTGGG[A/C]CCTCCCAGTTCTAAA	140432
rs546587694	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177372	TTCTGCTAGGCCAGG[C/T]GCGGTGACTCACTCT	140432
rs546946648	snp	C/G/T	3.29838e-05	0.00406092	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176876	TCGGCGTATGGTGCT[C/G/T]CTTCTCGGTGTCCTG	140432
rs547175983	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175903	TTTCCTTCCCGTTAA[G/T]GCTTAATAGCATTCC	140432
rs547887726	snp	C/G	0.000164769	0.0090751	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176699	CGCGCAGATGCCCTG[C/G]CGCACGTATGGGGCC	140432
rs547951079	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175940	TGTGTGTATCGCATT[G/T]TGTTTGTCCATTCAT	140432
rs548321071	snp	A/G	4.94173e-05	0.00497053	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176523	ATGGTTTTCGTCCTC[A/G]CAGATACAGTAGCGA	140432
rs549136564	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179051	GGAGACCCCCAGATG[C/T]TGGTGTCCATATTAG	140432
rs550102642	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179093	GCTGCTGATAAAGAC[A/G]CACCTGAGACTGGGT	140432
rs550801310	in-del	-/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179247	AGTGAAAGGGGTTTG[-/C]CCCTTATAAAACCAT	140432
rs550962184	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178075	TTTGAAATAAAAGTA[A/C]CACATGTAAACATTT	140432
rs551621530	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178323	GCCTCAGCCTCCTGA[C/G]TAGCTGGGATTACAG	140432
rs551718842	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178264	GCAGTTACATGATCC[C/T]GGCTCACTGCAACCT	140432
rs553174924	snp	A/C/G	3.30722e-05	0.00406635	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176220	GTGAGAATTATGGGA[A/C/G]ACCTAAGCCATGGGA	140432
rs554409781	snp	A/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179067	TGGTGTCCATATTAG[A/T]CCGTTTTCACGCTGC	140432
rs554947536	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178670	TACTAGAATGGAAGA[C/T]GAGATTCAGCTCACT	140432
rs555684696	snp	A/C	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177664	ATTAAAAAAAAAAAA[A/C]CCAAAAAAAAAGGCT	140432
rs557004684	in-del	-/AA			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177488	TCCATCCTTACTAAA[-/AA]TACAAAAATTACCTG	140432
rs558282290	snp	G/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177622	ACTGTACTCTAGCCT[G/T]GGTGACAGAGCGAGA	140432
rs558631844	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175418	GTTCTTAACTGATAT[C/T]CTTTATTTGCTGTTT	140432
rs558944393	snp	A/G	1.64746e-05	0.00287002	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176658	GTCCTTGCAGATGTC[A/G]GGCTGGTAATCCCAG	140432
rs559428611	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175930	TTCCATTGTGTGTGT[A/G]TATCGCATTTTGTTT	140432
rs560415786	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179021	GTGATTCAGTTGGAA[C/G]CCATCTTTTTTCTTG	140432
rs562664776	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179261	TGCCCTTATAAAACC[A/G]TCAGATCTCATGGGA	140432
rs562889526	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178947	TTCAGAGTGAGGTGC[C/G]TAAAAGCTGGCTGGA	140432
rs563071319	snp	A/G	1.87226e-05	0.00305956	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177226	CTTCCTGGAGAAGGT[A/G]GCGCTGCCATGTTTG	140432
rs564509369	snp	C/T			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176132	TCAACAGGCTGCTTC[C/T]CCCCAGTGTACATAC	140432
rs564687893	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175820	TTCACTTAGCAGTGT[C/T]GTCTTCAAGGTTCAT	140432
rs564848599	snp	C/T	3.29522e-05	0.00405894	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176615	ATTTGCAGCTGTCCC[C/T]GAAGCCACAGAAGCC	140432
rs565728375	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175330	TTTAAGGGAGAGGAT[A/G]TTAACATCAGCCAAA	140432
rs567049778	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178346	GATTACAGGTGTGTG[C/T]CACCACACCCAGCTA	140432
rs567584441	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178410	CATGTTGGCCAGGCT[A/G]GTGTGGAACTCCTGA	140432
rs568468685	snp	C/T	0.000399281	0.0141238	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176888	GCTCCTTCTCGGTGT[C/T]CTGCTCGAAGTCAGC	140432
rs568532809	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178326	TCAGCCTCCTGAGTA[C/G]CTGGGATTACAGGTG	140432
rs569410847	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177464	CCAGCCTGGCCAACA[C/T]AGCGAAACTCCATCC	140432
rs570754261	snp	C/T	0.000825886	0.0203042	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176169	GAGTCTTTCTTATCT[C/T]TTTTTTCCTAAAAGA	140432
rs571807224	in-del	-/TTT			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178211	TTTTTTTTTTTTTTT[-/TTT]GAGAAAGAGTCTCGC	140432
rs572819338	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179166	TGGCTAGGGAGGTCT[C/G]ACAATCCATGGTAGA	140432
rs573781403	in-del	-/TTT	0.392325	0.205532	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178190	GATAATCATTTTTAA[-/TTT]TTTTTTTTTTTTTTT	140432
rs573919993	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179235	AGAATGAGAACCAAG[C/T]GAAAGGGGTTTGCCC	140432
rs573956280	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178806	AGCTTACAGTGTAAA[G/T]AACAATTCATCATTT	140432
rs574073501	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177708	CCTCCCTTGACCTGC[C/T]TCCTGGCCCTCAGAT	140432
rs574133458	snp	A/C/G	5.24144e-05	0.00511907	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177127	TCGGGGTCGCAGGCC[A/C/G]GGCGCTTTCTGAGGC	140432
rs574953217	snp	C/G	3.29554e-05	0.00405914	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176351	AGATGCCGCCGGTTG[C/G]CTGGTCACAGATGTA	140432
rs575062482	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175607	TTAGGTATATATATA[C/T]TGATGTGTAACAGAG	140432
rs575270749	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177805	GATTCCTAAAAGGCC[A/C]CGGGTGGAATCATTC	140432
rs575920246	snp	G/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176528	TTTCGTCCTCGCAGA[G/T]ACAGTAGCGACCCTC	140432
rs575982734	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175778	GAAAAATCATACAGC[A/G]TATTGGTCATTTTGT	140432
rs577178341	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175435	TTTATTTGCTGTTTT[C/G]GTAACTCTTGAACCC	140432
rs745521093	snp	A/G	1.66885e-05	0.00288859	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176947	GGCTTCGCCGAGCGG[A/G]TGGACCTGTACACCA	140432
rs745581725	snp	G/T	3.73692e-05	0.00432241	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177016	TCGCCGTGAGCCGCC[G/T]TCTGCCAGCTGTGGA	140432
rs745646637	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178795	TGTGATGAATAAGCT[C/T]ACAGTGTAAAGAACA	140432
rs745789761	snp	A/G			intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176978	CGTCGAGGCTCTCAG[A/G]CGCCGCCTCCTCGCC	140432
rs746085348	snp	C/T	3.29647e-05	0.00405971	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176729	CCTTCCTCGCCATCC[C/T]CGAGGAGGAGTTGCC	140432
rs746114758	snp	G/T	4.94214e-05	0.00497074	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176652	CTTGTAGTCCTTGCA[G/T]ATGTCAGGCTGGTAA	140432
rs746357918	snp	A/G	1.86364e-05	0.00305251	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177224	TCCTTCCTGGAGAAG[A/G]TGGCGCTGCCATGTT	140432
rs746445835	snp	C/G	1.65935e-05	0.00288036	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176268	GTCTTCTGTGAAATG[C/G]GACTTGCCCCCACCT	140432
rs746655134	in-del	-/TTT			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178191	ATAATCATTTTTAAT[-/TTT]TTTTTTTTTTTTTTT	140432
rs746811807	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177298	GTCGCCCTTGCGTCG[C/G]TGCACGTGGGGCGTG	140432
rs746970105	snp	A/C/G	3.33263e-05	0.00408194	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176941	CCCACAGGCTTCGCC[A/C/G]AGCGGGTGGACCTGT	140432
rs747017556	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178996	GCTTGTACACTGGAC[C/T]GTCCTTTGTGTGATT	140432
rs747195599	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178927	TTATCTCCAGCTGTT[C/T]ATACTTCAGAGTGAG	140432
rs747338620	snp	A/G	1.64732e-05	0.0028699	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176626	TCCCCGAAGCCACAG[A/G]AGCCAGTCTCCTTGT	140432
rs747542296	snp	A/C	1.96825e-05	0.00313702	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177050	CCCGGGGCCTCGGTG[A/C]CACCCGCGGGGGCTG	140432
rs747823372	snp	A/G	1.65105e-05	0.00287315	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176144	TTCTCCCCAGTGTAC[A/G]TACAGACTTGAGTCT	140432
rs747860509	snp	A/C/G	3.6931e-05	0.00429699	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177220	GCCGTCCTTCCTGGA[A/C/G]AAGGTGGCGCTGCCA	140432
rs748070191	snp	C/T	1.64906e-05	0.00287142	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176861	TGCACTTGAGGATGG[C/T]CGGCGTATGGTGCTC	140432
rs748089321	snp	C/T	1.64833e-05	0.00287078	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176773	TTGGGCTTCAGGTAC[C/T]TCAGGTAGCTGTGGA	140432
rs748448691	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176451	GACTGGGTTTTGGAA[A/G]GCCTGGCGACATATG	140432
rs748940106	snp	A/G	3.64166e-05	0.00426696	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177108	GCTGCTGCTCTCTCC[A/G]TGCTCGGGGTCGCAG	140432
rs748982430	snp	C/T	1.65116e-05	0.00287324	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176126	TCTTACTCAACAGGC[C/T]GCTTCTCCCCAGTGT	140432
rs748995054	snp	C/G	1.95578e-05	0.00312706	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177042	GTGGAGGCCCCGGGG[C/G]CTCGGTGCCACCCGC	140432
rs749258700	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178659	ATCTCTTTACTTACT[A/G]GAATGGAAGATGAGA	140432
rs749612958	snp	C/G	5.72295e-05	0.00534897	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177233	GAGAAGGTGGCGCTG[C/G]CATGTTTGAGTCTCA	140432
rs749660730	in-del	-/TGCGTCACCCT	2.14011e-05	0.0032711	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177269	CCAACGGCCGTGGCG[-/TGCGTCACCCT]TGCGTCGCCCTTGCG	140432
rs749793696	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176433	ATGCCTGCACTTGGT[A/G]ACGACTGGGTTTTGG	140432
rs749811099	in-del	-/A	1.64735e-05	0.00286993	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176386	CGCGGGGTGGCCCGG[-/A]AGTGCTCCAGCGCGC	140432
rs749845859	snp	C/G	1.65586e-05	0.00287733	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176310	AAGCTTTTGCAGTTT[C/G]GCCATCAGTTCTTTG	140432
rs749879415	snp	A/G			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176517	CACTTCATGGTTTTC[A/G]TCCTCGCAGATACAG	140432
rs750110782	snp	A/G	1.64732e-05	0.0028699	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176589	CTTGTAATCGGAACG[A/G]TCGTGGAGGAATTTG	140432
rs750197564	in-del	-/G	1.64901e-05	0.00287137	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176843	CCTCCTGGACCCGCT[-/G]GCTGCACTTGAGGAT	140432
rs750294187	snp	G/T	0.000224678	0.0105966	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177182	TTTTGAAGAGGAAGG[G/T]GCATACCTGGTCTGC	140432
rs750394007	snp	C/G	1.82877e-05	0.00302383	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177106	CTGCTGCTGCTCTCT[C/G]CGTGCTCGGGGTCGC	140432
rs750761160	snp	A/G	1.64887e-05	0.00287125	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176827	TCCCGACCCCGCAGT[A/G]CCTCCTGGACCCGCT	140432
rs750797873	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178349	TACAGGTGTGTGCCA[C/G]CACACCCAGCTAACT	140432
rs751001347	snp	A/G	1.64969e-05	0.00287196	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176904	CTGCTCGAAGTCAGC[A/G]GTGGCCCCCATGTCC	140432
rs751047447	in-del	-/GCT	1.89354e-05	0.00307691	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98177089	GTCGCCCTCGTCCCC[-/GCT]GCTGCTGCTGCTCTC	140432
rs751143273	snp	C/T	3.29451e-05	0.00405851	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176502	CTCTTCCTCGCTTCC[C/T]ACTTCATGGTTTTCG	140432
rs751431106	snp	C/T	6.58892e-05	0.00573936	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176568	CCGTTCAATCTCCCA[C/T]CCGAGCTTGTAATCG	140432
rs751467561	snp	A/G	3.67154e-05	0.00428443	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177006	GCCCCTCCTGTCGCC[A/G]TGAGCCGCCTTCTGC	140432
rs751580428	snp	A/G	5.66856e-05	0.00532349	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177090	GTCGCCCTCGTCCCC[A/G]CTGCTGCTGCTCTCT	140432
rs751760297	snp	A/T	0.000215006	0.0103661	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176192	CTAAAAGAACAAAAA[A/T]ATTTATTTAAATGTG	140432
rs752037653	snp	A/C	1.64795e-05	0.00287045	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176707	TGCCCTGGCGCACGT[A/C]TGGGGCCCTTCCTCG	140432
rs752262474	snp	A/G	2.28815e-05	0.00338234	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177286	CGTCACCCTTGCGTC[A/G]CCCTTGCGTCGCTGC	140432
rs752328411	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178467	TCCTAAAATGTTGGT[A/C]TTACAGGCGTGAGCC	140432
rs752349921	in-del	-/T	1.71193e-05	0.00292564	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98177166	CCTTTCCGTCCAGGC[-/T]TTTTGAAGAGGAAGG	140432
rs752595311	snp	A/G	3.29457e-05	0.00405854	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176398	CGGAAGTGCTCCAGC[A/G]CGCAGCTCTCGCAGA	140432
rs752713236	snp	C/G	1.66161e-05	0.00288232	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176930	TGTCCTCTGGCCCCA[C/G]AGGCTTCGCCGAGCG	140432
rs752950268	snp	C/T	1.80071e-05	0.00300054	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176999	CCTCCTCGCCCCTCC[C/T]GTCGCCGTGAGCCGC	140432
rs753633234	snp	C/T	1.78267e-05	0.00298547	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177203	CCTGGTCTGCTTGGT[C/T]GGCCGTCCTTCCTGG	140432
rs753802105	snp	A/C/T	4.94184e-05	0.00497063	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176394	GGCCCGGAAGTGCTC[A/C/T]AGCGCGCAGCTCTCG	140432
rs753840619	in-del	-/A			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178102	ATTTAAAAAAATATT[-/A]TCAAGCACTTATTGT	140432
rs753841984	snp	C/T	1.654e-05	0.00287571	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176228	TATGGGAAACCTAAG[C/T]CATGGGAATTGGACA	140432
rs753861341	snp	A/G	0.000973636	0.0220425	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177272	ACGGCCGTGGCGTGC[A/G]TCACCCTTGCGTCGC	140432
rs754294962	snp	G/T	0.000148752	0.00862286	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176170	AGTCTTTCTTATCTC[G/T]TTTTTCCTAAAAGAA	140432
rs754458745	snp	C/G	1.64781e-05	0.00287033	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176702	GCAGATGCCCTGGCG[C/G]ACGTATGGGGCCCTT	140432
rs754473634	in-del	-/GT	1.78554e-05	0.00298787	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98177117	CTCTCCGTGCTCGGG[-/GT]CGCAGGCCGGGCGCT	140432
rs754737584	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178418	CCAGGCTGGTGTGGA[A/G]CTCCTGACCTCAGGT	140432
rs754739460	snp	C/G	5.39108e-05	0.00519158	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177114	GCTCTCTCCGTGCTC[C/G]GGGTCGCAGGCCGGG	140432
rs754767770	snp	C/T	1.6566e-05	0.00287797	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176237	CCTAAGCCATGGGAA[C/T]TGGACACTCATGGGG	140432
rs754829186	snp	A/G	3.29522e-05	0.00405894	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177204	CTGGTCTGCTTGGTC[A/G]GCCGTCCTTCCTGGA	140432
rs755067872	snp	A/G	1.64893e-05	0.0028713	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176849	GGACCCGCTGGCTGC[A/G]CTTGAGGATGGTCGG	140432
rs755576786	snp	C/G	1.6473e-05	0.00286988	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176591	TGTAATCGGAACGGT[C/G]GTGGAGGAATTTGCA	140432
rs755629957	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176519	CTTCATGGTTTTCGT[C/T]CTCGCAGATACAGTA	140432
rs755807213	in-del	-/GAAGAGGAAGGTGCATACCTG	6.85671e-05	0.00585481	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98177171	CCGTCCAGGCTTTTT[-/GAAGAGGAAGGTGCATACCTG]GTCTGCTTGGTCGGC	140432
rs755839729	snp	C/G/T	3.65092e-05	0.00427241	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177107	TGCTGCTGCTCTCTC[C/G/T]GTGCTCGGGGTCGCA	140432
rs756184785	snp	A/G	1.73273e-05	0.00294335	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177185	TGAAGAGGAAGGTGC[A/G]TACCTGGTCTGCTTG	140432
rs756463187	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176730	CTTCCTCGCCATCCC[C/T]GAGGAGGAGTTGCCC	140432
rs756958863	snp	G/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178571	TTATATAATGTAAAT[G/T]GATTCTAGTTCTTAT	140432
rs757002188	snp	A/C	1.64727e-05	0.00286986	intron-variant, stop-gained	FARP1, RNF113B	GRCh38.p7	13:98176507	CCTCGCTTCCCACTT[A/C]ATGGTTTTCGTCCTC	140432
rs757362220	snp	C/T	0.000333921	0.012917	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177097	TCGTCCCCGCTGCTG[C/T]TGCTCTCTCCGTGCT	140432
rs757647757	snp	C/T	1.64811e-05	0.00287059	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176714	GCGCACGTATGGGGC[C/T]CTTCCTCGCCATCCC	140432
rs757905776	snp	A/C	1.64893e-05	0.0028713	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176815	ATGTGGTCGTGCTCC[A/C]GACCCCGCAGTGCCT	140432
rs758189740	snp	A/G	1.65853e-05	0.00287964	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176252	TTGGACACTCATGGG[A/G]GTCTTCTGTGAAATG	140432
rs758225579	snp	A/G	1.6473e-05	0.00286988	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176400	GAAGTGCTCCAGCGC[A/G]CAGCTCTCGCAGAAA	140432
rs758293533	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178885	TCATCCCATCTTTCA[C/T]GTTGGAAGCTTTTCT	140432
rs758424880	snp	C/T	5.48391e-05	0.00523608	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177002	CCTCGCCCCTCCTGT[C/T]GCCGTGAGCCGCCTT	140432
rs758475708	snp	A/T	0.000149538	0.0086456	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176931	GTCCTCTGGCCCCAC[A/T]GGCTTCGCCGAGCGG	140432
rs759006975	snp	A/C	1.64768e-05	0.00287021	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176617	TTGCAGCTGTCCCCG[A/C]AGCCACAGAAGCCAG	140432
rs759532026	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176465	AGGCCTGGCGACATA[C/T]GAAACACCTGAATGG	140432
rs759601974	in-del	-/TCC	4.94181e-05	0.00497057	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98176518	ACTTCATGGTTTTCG[-/TCC]TCGCAGATACAGTAG	140432
rs759621971	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176536	TCGCAGATACAGTAG[C/T]GACCCTCTTCAAGCT	140432
rs759707265	snp	C/G			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175985	TTGGGTTGTTTACAC[C/G]TCTTGGCTTTTGCAA	140432
rs759781931	snp	C/G	7.8064e-05	0.00624707	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177061	GGTGCCACCCGCGGG[C/G]GCTGAGCCACTGTGT	140432
rs759961426	snp	C/T	8.83634e-05	0.00664634	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176987	TCTCAGGCGCCGCCT[C/T]CTCGCCCCTCCTGTC	140432
rs760628427	snp	A/C/T	3.29491e-05	0.00405877	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176371	TCACAGATGTAGCAG[A/C/T]GCGGGGTGGCCCGGA	140432
rs761529542	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176571	TTCAATCTCCCACCC[A/G]AGCTTGTAATCGGAA	140432
rs761618285	in-del	-/GAG	0.000131857	0.00811855	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98176731	TTCCTCGCCATCCCC[-/GAG]GAGGAGTTGCCCATG	140432
rs761633108	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176688	GCGCACAGTGGCGCG[C/T]AGATGCCCTGGCGCA	140432
rs761748326	snp	A/G	5.12422e-05	0.00506147	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177158	CTGCAGCCCCTTTCC[A/G]TCCAGGCTTTTTGAA	140432
rs761821798	snp	C/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175287	TGGATCTGTTGGTGT[C/T]TGTCTTGGGAGAGGA	140432
rs762063976	snp	A/T	6.61671e-05	0.00575145	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176194	AAAAGAACAAAAAAA[A/T]TTATTTAAATGTGAG	140432
rs762131725	snp	A/G	1.96219e-05	0.00313218	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177243	CGCTGCCATGTTTGA[A/G]TCTCAGGCTCCCAAC	140432
rs762568246	snp	A/G	3.29864e-05	0.00406105	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176886	GTGCTCCTTCTCGGT[A/G]TCCTGCTCGAAGTCA	140432
rs762608112	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176483	AACACCTGAATGGTA[C/T]TTCCTCTTCCTCGCT	140432
rs762788212	snp	A/T	1.64765e-05	0.00287019	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176677	TGGTAATCCCAGCGC[A/T]CAGTGGCGCGCAGAT	140432
rs762862368	in-del	-/T	1.80628e-05	0.00300517	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98177001	TCCTCGCCCCTCCTG[-/T]CGCCGTGAGCCGCCT	140432
rs762988535	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176551	CGACCCTCTTCAAGC[C/T]CCCGTTCAATCTCCC	140432
rs763203117	snp	A/G	1.90474e-05	0.00308599	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177084	CACTGTGTCGCCCTC[A/G]TCCCCGCTGCTGCTG	140432
rs763320348	snp	G/T	1.7051e-05	0.0029198	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177154	AGGCCTGCAGCCCCT[G/T]TCCGTCCAGGCTTTT	140432
rs764155455	snp	C/T	1.89354e-05	0.00307691	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177089	TGTCGCCCTCGTCCC[C/T]GCTGCTGCTGCTCTC	140432
rs764233372	snp	C/G	1.70638e-05	0.00292089	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177156	GCCTGCAGCCCCTTT[C/G]CGTCCAGGCTTTTTG	140432
rs764464377	snp	C/G	1.65466e-05	0.00287628	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176186	TTTTTCCTAAAAGAA[C/G]AAAAAAATTTATTTA	140432
rs764494395	snp	C/T			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176139	GCTGCTTCTCCCCAG[C/T]GTACATACAGACTTG	140432
rs764594031	snp	C/G	1.64787e-05	0.00287038	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176704	AGATGCCCTGGCGCA[C/G]GTATGGGGCCCTTCC	140432
rs764675566	snp	C/G	1.64871e-05	0.00287111	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176810	GGTAGATGTGGTCGT[C/G]CTCCCGACCCCGCAG	140432
rs765062045	in-del	-/GTG	1.64874e-05	0.00287113	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98176802	GATTCCCCGGTAGAT[-/GTG]GTCGTGCTCCCGACC	140432
rs765130665	snp	C/G	2.24717e-05	0.00335191	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177282	CGTGCGTCACCCTTG[C/G]GTCGCCCTTGCGTCG	140432
rs765312109	snp	C/T	7.06814e-05	0.00594438	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176988	CTCAGGCGCCGCCTC[C/T]TCGCCCCTCCTGTCG	140432
rs765635600	snp	C/T	1.64732e-05	0.0028699	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176397	CCGGAAGTGCTCCAG[C/T]GCGCAGCTCTCGCAG	140432
rs765725367	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178053	TGGGTGTGTAGCTGG[C/G]TTTCATTTTGAAATA	140432
rs765866455	snp	C/G/T	3.29567e-05	0.00405924	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176701	CGCAGATGCCCTGGC[C/G/T]CACGTATGGGGCCCT	140432
rs765956257	snp	C/G	3.29679e-05	0.00405991	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176781	CAGGTACCTCAGGTA[C/G]CTGTGGATTCCCCGG	140432
rs766260211	snp	C/T	1.7351e-05	0.00294537	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177186	GAAGAGGAAGGTGCA[C/T]ACCTGGTCTGCTTGG	140432
rs766324120	in-del	-/T	1.92959e-05	0.00310605	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98177075	GGCTGAGCCACTGTG[-/T]TCGCCCTCGTCCCCG	140432
rs766335721	snp	A/C/G	3.29453e-05	0.00405854	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176462	GGAAGGCCTGGCGAC[A/C/G]TATGAAACACCTGAA	140432
rs766765934	snp	C/T	1.74187e-05	0.00295111	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176981	CGAGGCTCTCAGGCG[C/T]CGCCTCCTCGCCCCT	140432
rs766840655	snp	A/G			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175719	TGACAACCACCATTC[A/G]ACTTTTTATGTAATT	140432
rs767022586	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177797	TTTCAACAGATTCCT[A/G]AAAGGCCACGGGTGG	140432
rs767093650	snp	A/C	1.6473e-05	0.00286988	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176587	AGCTTGTAATCGGAA[A/C]GGTCGTGGAGGAATT	140432
rs767322147	in-del	-/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178513	AAATATTTTTAACCC[-/T]TTTTTTTTCTTGAGT	140432
rs767326857	snp	A/C	0.000148288	0.00860943	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176694	AGTGGCGCGCAGATG[A/C]CCTGGCGCACGTATG	140432
rs767634227	snp	A/T	1.65414e-05	0.00287583	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176202	AAAAAAATTTATTTA[A/T]ATGTGAGAATTATGG	140432
rs767681603	snp	A/G	0.000103121	0.00717983	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177174	TCCAGGCTTTTTGAA[A/G]AGGAAGGTGCATACC	140432
rs768072038	snp	G/T	1.64969e-05	0.00287196	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176902	TCCTGCTCGAAGTCA[G/T]CGGTGGCCCCCATGT	140432
rs768247428	snp	G/T	1.959e-05	0.00312963	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177047	GGCCCCGGGGCCTCG[G/T]TGCCACCCGCGGGGG	140432
rs768572290	snp	C/T	1.65121e-05	0.00287329	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176133	CAACAGGCTGCTTCT[C/T]CCCAGTGTACATACA	140432
rs768583405	snp	A/G	3.29544e-05	0.00405908	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176685	CCAGCGCACAGTGGC[A/G]CGCAGATGCCCTGGC	140432
rs768639327	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178934	CAGCTGTTTATACTT[C/G]AGAGTGAGGTGCCTA	140432
rs768653186	snp	C/G	1.6483e-05	0.00287076	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176761	ATGGACGTGTCCTTG[C/G]GCTTCAGGTACCTCA	140432
rs768873844	snp	C/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177318	CGTGGGGCGTGGGCC[C/G]TCCCAGTTCTAAAAA	140432
rs768979308	snp	A/G	1.65176e-05	0.00287376	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176326	GCCATCAGTTCTTTG[A/G]CGGGGTTAAAGATGC	140432
rs769030366	snp	A/C	1.9158e-05	0.00309494	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177235	GAAGGTGGCGCTGCC[A/C]TGTTTGAGTCTCAGG	140432
rs769660454	snp	C/T	3.73755e-05	0.00432277	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177017	CGCCGTGAGCCGCCT[C/T]CTGCCAGCTGTGGAG	140432
rs770024902	snp	C/G	3.29451e-05	0.00405851	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176541	GATACAGTAGCGACC[C/G]TCTTCAAGCTCCCGT	140432
rs770114314	snp	C/T	1.70918e-05	0.00292329	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177143	GGCGCTTTCTGAGGC[C/T]TGCAGCCCCTTTCCG	140432
rs770412484	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179186	TCCATGGTAGAAGGT[A/G]AAAGGCATGTCTCGC	140432
rs770505949	snp	C/T	1.6607e-05	0.00288153	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176275	GTGAAATGGGACTTG[C/T]CCCCACCTTCTGCAG	140432
rs770645931	snp	C/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175688	ACAGCTCCCCACTCC[C/T]GCTCTTCCTAACCCC	140432
rs770735775	snp	A/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177284	TGCGTCACCCTTGCG[A/T]CGCCCTTGCGTCGCT	140432
rs771241422	snp	C/T	0.000115303	0.00759199	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176533	TCCTCGCAGATACAG[C/T]AGCGACCCTCTTCAA	140432
rs771288194	snp	C/G	1.96415e-05	0.00313375	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177051	CCGGGGCCTCGGTGC[C/G]ACCCGCGGGGGCTGA	140432
rs771353711	in-del	-/CCCTTGCGTCG	0.000198068	0.0099496	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177275	CCGTGGCGTGCGTCA[-/CCCTTGCGTCG]CCCTTGCGTCGCCCT	140432
rs771437938	in-del	-/T	1.64727e-05	0.00286986	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176419	CTCTCGCAGAAATAA[-/T]GCCTGCACTTGGTGA	140432
rs771683618	snp	G/T	3.30295e-05	0.0040637	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176159	ATACAGACTTGAGTC[G/T]TTCTTATCTCTTTTT	140432
rs771819119	snp	A/G	1.64836e-05	0.0028708	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176776	GGCTTCAGGTACCTC[A/G]GGTAGCTGTGGATTC	140432
rs772052064	snp	C/T	0.000115436	0.00759637	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176862	GCACTTGAGGATGGT[C/T]GGCGTATGGTGCTCC	140432
rs772258429	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177384	AGGCGCGGTGACTCA[C/T]TCTTGTAATCCCGGG	140432
rs772284861	in-del	-/C	1.64727e-05	0.00286986	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176564	GCTCCCGTTCAATCT[-/C]CCACCCGAGCTTGTA	140432
rs772298086	snp	A/G	1.6473e-05	0.00286988	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176525	GGTTTTCGTCCTCGC[A/G]GATACAGTAGCGACC	140432
rs772636294	snp	A/C	1.65162e-05	0.00287365	intron-variant, stop-lost	FARP1, RNF113B	GRCh38.p7	13:98176165	ACTTGAGTCTTTCTT[A/C]TCTCTTTTTTCCTAA	140432
rs773053844	snp	C/G	1.64841e-05	0.00287085	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176777	GCTTCAGGTACCTCA[C/G]GTAGCTGTGGATTCC	140432
rs773120621	snp	A/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175578	CCTTAACCATTTTTA[A/T]GTGTTCACTCATATT	140432
rs773143765	snp	A/G	1.64909e-05	0.00287144	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176866	TTGAGGATGGTCGGC[A/G]TATGGTGCTCCTTCT	140432
rs773255110	snp	A/C/T	6.58896e-05	0.00573943	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176458	TTTTGGAAGGCCTGG[A/C/T]GACATATGAAACACC	140432
rs773837308	snp	A/G	0.000705225	0.0187647	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176976	CACGTCGAGGCTCTC[A/G]GGCGCCGCCTCCTCG	140432
rs773880195	in-del	-/TCTT	1.65138e-05	0.00287343	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176157	ACATACAGACTTGAG[-/TCTT]TCTTATCTCTTTTTT	140432
rs774067876	snp	G/T	3.92688e-05	0.0044309	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177048	GCCCCGGGGCCTCGG[G/T]GCCACCCGCGGGGGC	140432
rs774163109	snp	G/T	1.64773e-05	0.00287026	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176687	AGCGCACAGTGGCGC[G/T]CAGATGCCCTGGCGC	140432
rs774299024	snp	C/T	1.64836e-05	0.0028708	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176772	CTTGGGCTTCAGGTA[C/T]CTCAGGTAGCTGTGG	140432
rs774363097	in-del	-/T	3.29451e-05	0.00405851	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176489	GAATGGTATTTCCTC[-/T]TTCCTCGCTTCCCAC	140432
rs774412431	snp	G/T	1.93673e-05	0.00311179	intron-variant, utr-variant-5-prime	FARP1, RNF113B	GRCh38.p7	13:98177239	GTGGCGCTGCCATGT[G/T]TGAGTCTCAGGCTCC	140432
rs774664158	snp	A/C	1.70723e-05	0.00292162	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177157	CCTGCAGCCCCTTTC[A/C]GTCCAGGCTTTTTGA	140432
rs774767836	snp	C/T	1.65181e-05	0.00287381	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176327	CCATCAGTTCTTTGG[C/T]GGGGTTAAAGATGCC	140432
rs774922206	snp	A/G	1.64933e-05	0.00287165	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176884	TGGTGCTCCTTCTCG[A/G]TGTCCTGCTCGAAGT	140432
rs775287438	snp	A/G	1.68949e-05	0.0029064	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176964	GGACCTGTACACCAC[A/G]TCGAGGCTCTCAGGC	140432
rs775399101	snp	G/T			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176061	CGGATTTCAATTCTT[G/T]TGGTTACATACTCAG	140432
rs775649538	in-del	-/A	0.000757682	0.0194491	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98176689	CGCACAGTGGCGCGC[-/A]GATGCCCTGGCGCAC	140432
rs775668067	snp	C/T	3.83017e-05	0.004376	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177080	GAGCCACTGTGTCGC[C/T]CTCGTCCCCGCTGCT	140432
rs775812030	snp	G/T	1.65847e-05	0.0028796	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176283	GGACTTGCCCCCACC[G/T]TCTGCAGCCTGAAGC	140432
rs775900760	snp	C/G	1.70615e-05	0.00292069	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177149	TTCTGAGGCCTGCAG[C/G]CCCTTTCCGTCCAGG	140432
rs776077151	snp	C/T	1.65211e-05	0.00287407	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176174	TTTCTTATCTCTTTT[C/T]TCCTAAAAGAACAAA	140432
rs776111580	in-del	-/TT			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178192	TAATCATTTTTAATT[-/TT]TTTTTTTTTTTTTTT	140432
rs776151178	snp	A/G	3.29739e-05	0.00406028	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176805	TCCCCGGTAGATGTG[A/G]TCGTGCTCCCGACCC	140432
rs776731723	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179070	TGTCCATATTAGTCC[A/G]TTTTCACGCTGCTGA	140432
rs776956246	snp	C/T	1.7361e-05	0.00294621	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177130	GGGTCGCAGGCCGGG[C/T]GCTTTCTGAGGCCTG	140432
rs777005575	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176534	CCTCGCAGATACAGT[A/G]GCGACCCTCTTCAAG	140432
rs777202505	snp	A/G	1.95498e-05	0.00312642	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177060	CGGTGCCACCCGCGG[A/G]GGCTGAGCCACTGTG	140432
rs777223809	snp	G/T	1.64727e-05	0.00286986	intron-variant, stop-gained	FARP1, RNF113B	GRCh38.p7	13:98176409	CAGCGCGCAGCTCTC[G/T]CAGAAATAATGCCTG	140432
rs777292374	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178542	GTTTATCTTCAAGTT[A/G]TGAAATAATTCATTT	140432
rs777383980	snp	C/G	3.71865e-05	0.00431183	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177223	GTCCTTCCTGGAGAA[C/G]GTGGCGCTGCCATGT	140432
rs777645972	snp	C/T	1.66557e-05	0.00288575	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176940	CCCCACAGGCTTCGC[C/T]GAGCGGGTGGACCTG	140432
rs778236848	snp	C/G	3.29451e-05	0.00405851	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176526	GTTTTCGTCCTCGCA[C/G]ATACAGTAGCGACCC	140432
rs778324957	in-del	-/TGGTCTGCT	0.000418049	0.0144516	intron-variant, cds-indel	FARP1, RNF113B	GRCh38.p7	13:98177190	AGGAAGGTGCATACC[-/TGGTCTGCT]TGGTCGGCCGTCCTT	140432
rs778664498	snp	C/T	1.65105e-05	0.00287315	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176141	TGCTTCTCCCCAGTG[C/T]ACATACAGACTTGAG	140432
rs778672395	snp	A/G	9.17187e-05	0.00677133	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177217	TCGGCCGTCCTTCCT[A/G]GAGAAGGTGGCGCTG	140432
rs778725590	snp	C/T	1.7764e-05	0.00298022			GRCh38.p7	13:98177119	CTCCGTGCTCGGGGT[C/T]GCAGGCCGGGCGCTT	140432
rs778896186	snp	A/G	1.64912e-05	0.00287147	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176860	CTGCACTTGAGGATG[A/G]TCGGCGTATGGTGCT	140432
rs778897644	snp	C/G	3.31439e-05	0.00407073	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176240	AAGCCATGGGAATTG[C/G]ACACTCATGGGGGTC	140432
rs779033803	snp	C/T	1.65894e-05	0.00288	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176926	CCCATGTCCTCTGGC[C/T]CCACAGGCTTCGCCG	140432
rs779277632	in-del	-/TTTT			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178190	GATAATCATTTTTAA[-/TTTT]TTTTTTTTTTTTTTT	140432
rs779408892	in-del	-/CCCTTGCGTCG	0.000198068	0.0099496	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177276	CCGTGGCGTGCGTCA[-/CCCTTGCGTCG]CCCTTGCGTCGCTGC	140432
rs779584584	snp	A/G	1.6473e-05	0.00286988	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176592	GTAATCGGAACGGTC[A/G]TGGAGGAATTTGCAG	140432
rs779793046	snp	A/G	4.96036e-05	0.00497989	intron-variant	FARP1, RNF113B	GRCh38.p7	13:98176225	AATTATGGGAAACCT[A/G]AGCCATGGGAATTGG	140432
rs779802187	snp	A/G	1.92132e-05	0.00309939	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177031	TTCTGCCAGCTGTGG[A/G]GGCCCCGGGGCCTCG	140432
rs779890630	snp	A/T	1.65181e-05	0.00287381	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176117	TCTCTCTCATCTTAC[A/T]CAACAGGCTGCTTCT	140432
rs780139773	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178844	TTCTCTTAGGATAGT[A/G]ATTCTAGATTTTTCT	140432
rs780286201	snp	A/G	1.64904e-05	0.00287139	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176840	GTGCCTCCTGGACCC[A/G]CTGGCTGCACTTGAG	140432
rs780544120	snp	C/G	3.78122e-05	0.00434795	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177229	CCTGGAGAAGGTGGC[C/G]CTGCCATGTTTGAGT	140432
rs780669305	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176513	TTCCCACTTCATGGT[C/T]TTCGTCCTCGCAGAT	140432
rs780797199	snp	C/T	1.64727e-05	0.00286986	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176427	GAAATAATGCCTGCA[C/T]TTGGTGACGACTGGG	140432
rs781027219	in-del	-/A	1.7161e-05	0.0029292	intron-variant, frameshift-variant	FARP1, RNF113B	GRCh38.p7	13:98177139	GCCGGGCGCTTTCTG[-/A]GGCCTGCAGCCCCTT	140432
rs781523845	snp	A/G	0.000115313	0.0075923	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176649	CTCCTTGTAGTCCTT[A/G]CAGATGTCAGGCTGG	140432
rs781719261	snp	C/T	1.64822e-05	0.00287068	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176726	GGCCCTTCCTCGCCA[C/T]CCCCGAGGAGGAGTT	140432
rs796458371	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178228	TGAGAAAGAGTCTCG[C/T]TCTGTCGCCCAGGCT	140432
rs796886353	in-del	-/A			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177675	AAAAACCAAAAAAAA[-/A]GGCTTCTCCCGCCCT	140432