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

IFT122

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs872024	snp	C/T	0.0178098	0.0926698	downstream-variant-500B	IFT122	GRCh38.p7	3:129520526	CGGCTCCGAGTTGTT[C/T]GTGGCAGCCTGCTGG	55764
rs1872104	snp	C/G	0.121717	0.214577	intron-variant	IFT122	GRCh38.p7	3:129502506	TACAGGATCCTGTCA[C/G]CCACCTTGTGTGTCT	55764
rs1872105	snp	C/T	0.278133	0.248412	intron-variant	IFT122	GRCh38.p7	3:129502139	CCTGCAGGAAGTCTT[C/T]CCTGTCCTCCTGGCC	55764
rs1872106	snp	C/G	0.319856	0.240042	downstream-variant-500B	IFT122	GRCh38.p7	3:129520836	GACAAGAGAAAATAC[C/G]TGGGTCCAAAGAAGA	55764
rs1872107	snp	C/G/T	0.121717	0.214577	downstream-variant-500B	IFT122	GRCh38.p7	3:129520959	GCCCCACAGAGCAGC[C/G/T]CCAGCCCAATGGAGA	55764
rs2260840	snp	C/G/T	0.499831	0.00918375	intron-variant	IFT122	GRCh38.p7	3:129515416	CAGGCCCCAGGGGCC[C/G/T]GAAGCCAGAGTCCAG	55764
rs2285349	snp	C/T	0.280785	0.248097	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458503	AGAAGCTAACACTTA[C/T]TAGGTACCTTAAAGA	55764
rs2285350	snp	G/T	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129469180	ATCCCGTAAGACTGA[G/T]TGATGGGTTGGGCCA	55764
rs2285351	snp	C/T	0.266546	0.249452	intron-variant	IFT122	GRCh38.p7	3:129469237	CTGTACAACATTTGG[C/T]AACCTGAGGCCAGGA	55764
rs2285352	snp	A/C	0.29046	0.246704	intron-variant	IFT122	GRCh38.p7	3:129481929	TTTCCTTGCCAATGG[A/C]AACCGAAGGCTCTGA	55764
rs2285353	snp	A/C	0.214843	0.247516	intron-variant	IFT122	GRCh38.p7	3:129492024	AATCTGTGCTTGCTC[A/C]CTTCCTCTCCTCTGT	55764
rs2285354	snp	C/G	0.413622	0.18918	intron-variant	IFT122	GRCh38.p7	3:129492134	ATTCTTTATTTCTTC[C/G]CCACAGGCCTTCATC	55764
rs2285355	snp	C/G	0.265727	0.249505	intron-variant	IFT122	GRCh38.p7	3:129512590	GCAGGGAGGCCCAGG[C/G]GCCCAGGCCAAGAGA	55764
rs2301570	snp	C/T	0.148056	0.228271	intron-variant	IFT122	GRCh38.p7	3:129476820	AGAGGCAGGTCCAGA[C/T]CTTGGGAAGAGGGAC	55764
rs2307292	snp	A/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439948	GGGCGCTTTCGCAAC[A/T]TTCAGACCTCGGTTG	55764
rs2307297	snp	C/T	0.000861738	0.0207395	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439803	CTGGAGAGTCTGAGT[C/T]TGGGGGACCGCGGAG	55764
rs2311394	snp	C/T	0.328616	0.237317	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440996	tcattttgagcacct[C/T]tctgatcatacctgc	55764
rs2625940	snp	A/T	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129512704	TGCTTCTTCCATTTC[A/T]GTCACACCCTCATCT	55764
rs2625941	snp	C/T	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129501131	TCCGGTGTGCTGAGT[C/T]CCAAGGCTGAATCCA	55764
rs2626007	snp	A/G	0.121717	0.214577	intron-variant	IFT122	GRCh38.p7	3:129518136	TGGGGGCACCACGGG[A/G]ATGCCAAAGAATGAA	55764
rs2626008	snp	A/C	0.121717	0.214577	intron-variant	IFT122	GRCh38.p7	3:129518135	GGGGGCACCACGGGA[A/C]TGCCAAAGAATGAAG	55764
rs2713619	snp	C/T	0.117886	0.21224	intron-variant	IFT122	GRCh38.p7	3:129513921	CTGCACACCCTTCCC[C/T]GAGGGCCTGGTGGGC	55764
rs2713620	snp	C/T	0.119281	0.213102	intron-variant	IFT122	GRCh38.p7	3:129513845	TCAGCCAGAGGCTGA[C/T]GAGCCTTTGTGCTCT	55764
rs2713621	snp	A/C	0.499713	0.0119774	intron-variant	IFT122	GRCh38.p7	3:129505288	CAAACACCCAACTTC[A/C]ATTAGAAGGCTAAAT	55764
rs2713622	snp	A/G	0.17332	0.23795	intron-variant	IFT122	GRCh38.p7	3:129503364	TAGTGGTTGTGGGGT[A/G]GGGGCAGAGAAGGGA	55764
rs3138322	snp	C/G	0.281049	0.248064	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441944	CTGCCCCTTTTAGGC[C/G]GAGCATGAGCTCTGC	55764
rs3138323	snp	C/G	0.280785	0.248097	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441438	agagagtggtgaaga[C/G]acaacgagataaagg	55764
rs3138324	snp	C/G	0.0614824	0.164198	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441351	CACAAAAGAGAGGAC[C/G]CGTCTCCAACGTGAG	55764
rs3138325	snp	C/T	0.00336134	0.0408579	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441350	ACAAAAGAGAGGACC[C/T]GTCTCCAACGTGAGC	55764
rs3138326	snp	A/T	0.280785	0.248097	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441186	GCTGAATGATTTTCA[A/T]AGTCAGGCCAAGACC	55764
rs3138327	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441132	AAAACAGACTGCTAT[C/G]TTATAGATTTAGGCG	55764
rs3138328	snp	A/G	0.0539704	0.155153	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441101	ATAACAATGGAATAG[A/G]ACATTAAATAACTGA	55764
rs3138329	snp	A/T	0.0126979	0.078662	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441000	gtgctcattttgagc[A/T]cctttctgatcatac	55764
rs3138330	snp	A/G	0.0110494	0.0735024	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440836	TGATTTTATCTTAAC[A/G]tttagagcaagtgac	55764
rs3138331	snp	C/T	0.281049	0.248064	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440835	GATTTTATCTTAACA[C/T]TTAGAGCAAGTGACA	55764
rs3138332	snp	C/T	0.0236746	0.106192	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440786	gtaataaagtttcct[C/T]gtaaaatgtgaaatc	55764
rs3138333	snp	C/T	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440634	ATGAATCCAAGGCAG[C/T]GACAGGGCCAGACCG	55764
rs3138334	snp	C/T	0.0614824	0.164198	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440125	AAGCAGCAAAAGCAA[C/T]GGTGGCACTGGAGCC	55764
rs3138335	snp	C/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439443	AGGAAGTCATTAGAC[C/T]ACGTGTGTGATAGGA	55764
rs3138336	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439426	CGTGTGTGATAGGAG[A/G]TTAAGATTTACCTAC	55764
rs3138337	snp	G/T	0.0459516	0.144445	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439425	GTGTGTGATAGGAGG[G/T]TAAGATTTACCTACT	55764
rs3138338	snp	C/T	0.278664	0.248351	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438921	tttgagatgaggtct[C/T]gctctgtcacccagg	55764
rs3733144	snp	C/T	0	0	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506922	CTCCAGATTCTTACT[C/T]ATCCCAGCCAGGAAA	55764
rs3733145	snp	C/T	0.191775	0.243125	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507124	TGAGCTCTGCATGCC[C/T]ATCTGTCCTGTGGGA	55764
rs3774764	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129449806	AATAAAGTTTACTTT[C/T]CTGGCCATTAGCAGA	55764
rs3774765	snp	C/G	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129449811	AGTTTACTTTCCTGG[C/G]CATTAGCAGACTTCA	55764
rs3774766	snp	C/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129451601	TTTAGGAGGGCCTGC[C/G]TTGATCAATCATATA	55764
rs3774767	snp	C/G	0.463774	0.129618	intron-variant	IFT122	GRCh38.p7	3:129474067	GCTAGGGAAAGTTTT[C/G]GTTGCTAGGCATTTG	55764
rs3774768	snp	C/T	0.463774	0.129618	intron-variant	IFT122	GRCh38.p7	3:129482251	GTTGTAGGCGTTGTT[C/T]AGTGGAGTCATCCAG	55764
rs3774769	snp	A/G	0.213937	0.247385	intron-variant	IFT122	GRCh38.p7	3:129493428	CTCTGTGCCACATGC[A/G]TGATTTATGTGAATG	55764
rs3774770	snp	C/G	0.290718	0.246662	intron-variant	IFT122	GRCh38.p7	3:129495737	CAGAAAGGATGTGGG[C/G]AAACTGGTAAACAAA	55764
rs3774771	snp	A/G	0.215446	0.2476	intron-variant	IFT122	GRCh38.p7	3:129495814	TAAGGCTGACACCAA[A/G]GGGGCAGACTATGGC	55764
rs3774772	snp	A/G	0.0551013	0.156571	intron-variant	IFT122	GRCh38.p7	3:129495846	GTTCAGACCTTCATC[A/G]GTGACAGGGCTGGAT	55764
rs3774773	snp	C/T	0.460252	0.135255	intron-variant	IFT122	GRCh38.p7	3:129495926	GGCTTCAGGGCTGTC[C/T]CCCACAAATCCTCTC	55764
rs3774774	snp	A/G	0.498133	0.030494	intron-variant	IFT122	GRCh38.p7	3:129497829	TGATTAACGTGGCAT[A/G]TTTTTGTTTACTTGA	55764
rs3774775	snp	A/C	0.192088	0.2432	intron-variant	IFT122	GRCh38.p7	3:129497846	TTTTGTTTACTTGAA[A/C]ATTGCTTCCCAAGAT	55764
rs3774776	snp	G/T	0.0490535	0.14873	intron-variant	IFT122	GRCh38.p7	3:129498348	CTCCAGCTGCCACCC[G/T]CATTTCACCAGCCAG	55764
rs3774778	snp	G/T	0.0681886	0.171594	intron-variant	IFT122	GRCh38.p7	3:129501705	TGCTTTCCAGATGTG[G/T]CTATAAAAGGTGTCT	55764
rs3774779	snp	C/G	0.265727	0.249505	intron-variant	IFT122	GRCh38.p7	3:129503446	GTGGCCAGCCTCAGG[C/G]TGGCAGAAGCAGCTG	55764
rs3774780	snp	G/T	0.187685	0.242109	intron-variant	IFT122	GRCh38.p7	3:129505263	ACCTGATTTTTCTGT[G/T]TTGCTGCCTATTTAG	55764
rs3774782	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512083	atctatctaggtgtc[A/G]gtttcctcatcagta	55764
rs3774783	snp	C/T	0.26518	0.249539	intron-variant	IFT122	GRCh38.p7	3:129513511	GTCTCCGTCTTTCCC[C/T]GTAGGAGCAGTCAGG	55764
rs3774784	snp	C/T	0.00755907	0.0610114	intron-variant	IFT122	GRCh38.p7	3:129518252	TGGCAGTGAAAGCCC[C/T]GGGGCACAGCTCAGC	55764
rs3806711	snp	A/G	0.386123	0.209692	intron-variant	IFT122	GRCh38.p7	3:129496202	AGGTTCATGGGGGCC[A/G]TCCCAATGCAAAAGG	55764
rs3821913	snp	C/T	0.215446	0.2476	intron-variant	IFT122	GRCh38.p7	3:129494074	TTCTTGTCCTGCTGA[C/T]GGGGGGAAAGAACCT	55764
rs3821914	snp	A/G	0.499642	0.0133738	intron-variant	IFT122	GRCh38.p7	3:129501144	GGGACTCAGCACACC[A/G]GACCTTGAGGGGGAA	55764
rs3821915	snp	A/G	0.198324	0.244601	intron-variant	IFT122	GRCh38.p7	3:129501153	CACACCGGACCTTGA[A/G]GGGGAAGGCTTTGTC	55764
rs3832258	in-del	-/AGA			cds-indel	IFT122	GRCh38.p7	3:129488367	GGCCATGGAAGCGCT[-/AGA]AGGTTTAGATTTTGA	55764
rs3836535	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129496398	CAATGAGGGTCTTCC[-/C]TTCCATCAAGGGGCT	55764
rs3836536	in-del	-/C	0.151001	0.229563	intron-variant	IFT122	GRCh38.p7	3:129497821	TCTAGTCCTGATTAA[-/C]GTGGCATATTTTTGT	55764
rs3836537	in-del	-/GCA			intron-variant	IFT122	GRCh38.p7	3:129499422	CAGCCTCACTCTGAA[-/GCA]TGTGGTATCACCCAT	55764
rs3836538	in-del	-/ACCTC/ACCTG	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129504912	GTGAGGCATGGTCTC[-/ACCTC/ACCTG]TACTGAGAATAGAAA	55764
rs4352374	snp	A/G	0.0422008	0.138995	intron-variant	IFT122	GRCh38.p7	3:129489469	ACAAGGGAAGTGATC[A/G]TTGTGTAACAATGAT	55764
rs4441648	snp	C/G	0.284471	0.247612	intron-variant	IFT122	GRCh38.p7	3:129499605	GCCCCAAATAGTCTA[C/G]AAAGTGTTGTTTAGC	55764
rs4456858	snp	A/C	0.267364	0.249396	intron-variant	IFT122	GRCh38.p7	3:129447415	cctgggatcaacaga[A/C]aggaatgtctgggtt	55764
rs4600811	snp	G/T	0.264358	0.249587	intron-variant	IFT122	GRCh38.p7	3:129487416	GTCTCGGTCTCCTGG[G/T]CTGTAGCCAGGGAGA	55764
rs4640556	snp	A/G	0.499673	0.0127754	intron-variant	IFT122	GRCh38.p7	3:129487455	CTACTGCACAGGACT[A/G]TGGGGACAGCCAAAA	55764
rs4688850	snp	C/T	0.241053	0.24984	intron-variant	IFT122	GRCh38.p7	3:129451462	CTCCTACTTGAAAGC[C/T]CAGAGTTCTGTGACT	55764
rs6439183	snp	G/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129471158	GTGAAGCCTTTAATT[G/T]CGTAGCATCCTTATT	55764
rs6439184	snp	A/G	0.499741	0.0113788	intron-variant	IFT122	GRCh38.p7	3:129518742	CTGGGGTCAGCAGGG[A/G]CTCTCGCCCCTGTCT	55764
rs6767707	snp	A/G	0.463774	0.129618	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475606	gcagtaagccaagat[A/G]gcgccactgcactcc	55764
rs6770233	snp	C/T	0.4983	0.0291038	intron-variant	IFT122	GRCh38.p7	3:129466798	GTGAGTCACTGCACC[C/T]GGCCCCCAGGGGCTC	55764
rs6771214	snp	A/G	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129470761	ttttagtagagacgg[A/G]gtttctccatgttgg	55764
rs6774638	snp	C/G	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129447607	aacctctgtctcccg[C/G]gttcaagcaattctc	55764
rs6777036	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129447725	accatgttggtcagg[C/T]tggcctcaaactcct	55764
rs6777052	snp	C/T	0.281577	0.247998	intron-variant	IFT122	GRCh38.p7	3:129447757	acctcgtgatccgcc[C/T]gcctcggcctcccaa	55764
rs6781214	snp	A/G	0.21725	0.247846	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507253	TTGGGCCAGTGCCTT[A/G]TGCTTCTGATAGGAG	55764
rs6781426	snp	G/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129479566	GGCTGCCTGGGTGGG[G/T]GTTTGCATTGAAGAT	55764
rs6784396	snp	A/T	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129471077	GGAAATGCCAAGGAT[A/T]AGAGTAAAGGTGCTG	55764
rs6786176	snp	C/G	0.282105	0.24793	intron-variant	IFT122	GRCh38.p7	3:129496372	GGTTCAAAGAGGCTT[C/G]GGTACACTGGGCAAT	55764
rs6786195	snp	C/T	0.281313	0.248031	intron-variant	IFT122	GRCh38.p7	3:129452341	AAAAGGTAAATTAAG[C/T]AGTATGCTGGAAGGT	55764
rs6789079	snp	A/G	0.498832	0.0241331	intron-variant	IFT122	GRCh38.p7	3:129461746	CTTGTGCAATTTGTC[A/G]TCATTACTGGTTTAG	55764
rs6789779	snp	A/G	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129497290	ataataaaaTGCCTG[A/G]CCTTGGTGCCCCAGA	55764
rs6795952	snp	C/G	0.162253	0.234095	intron-variant	IFT122	GRCh38.p7	3:129498703	CATACATTGACTGTA[C/G]TTTTCTGACACATGA	55764
rs6799876	snp	G/T	0.213453	0.247314	intron-variant	IFT122	GRCh38.p7	3:129500101	CCCCGAGAAGCATTT[G/T]GCAGCATGTCATCAC	55764
rs6802395	snp	G/T	0.498158	0.0302955	intron-variant	IFT122	GRCh38.p7	3:129497279	GTCAAAAAAAAATAA[G/T]AAAATGCCTGGCCTT	55764
rs6805886	snp	A/C	0	0	intron-variant	IFT122	GRCh38.p7	3:129466818	CCCAGGGGCTCCTTG[A/C]CAGGATTTTAAATTA	55764
rs6809071	snp	C/T	0.216349	0.247725	intron-variant	IFT122	GRCh38.p7	3:129508466	ggaaggactgtcacc[C/T]ccatgttacagatga	55764
rs7429444	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129489482	TCGTTGTGTAACAAT[A/G]ATCTAGATTATATTT	55764
rs7610149	snp	G/T	0.463666	0.129795	intron-variant	IFT122	GRCh38.p7	3:129483801	GAATGGCAGCTGTGA[G/T]GTCGTGGGAGGCAGT	55764
rs7611963	snp	C/G	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129469119	TCATAGCAGGGGACT[C/G]AGTGAAACAGCAGAT	55764
rs7612530	snp	A/G	0.499673	0.0127754	intron-variant	IFT122	GRCh38.p7	3:129469482	ATTTTCTGAGATTCT[A/G]TTACTATTAATTATA	55764
rs7622607	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129473994	gcTGCTAGCCTTCCA[C/T]GTCGTGATTCATAAG	55764
rs7622615	snp	G/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129474013	GTGATTCATAAGAAT[G/T]TTTAGTTTTCTTGTT	55764
rs7626212	snp	C/T	0.126564	0.217402	intron-variant	IFT122	GRCh38.p7	3:129478660	tttgggaggctaagg[C/T]gggaggaatgcttga	55764
rs7628918	snp	A/G	0.463666	0.129795	intron-variant	IFT122	GRCh38.p7	3:129482849	CCTAGCTCAGTGTTG[A/G]GCACAAAATGGGGCC	55764
rs7629620	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470872	gccaccacgcctggc[C/T]GGAGATGTGATTATA	55764
rs7629621	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470878	acgcctggctGGAGA[C/T]GTGATTATAAAGGAC	55764
rs7629992	snp	C/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129471249	CATTTCTTCTACCCC[C/T]GCCTTACCATTGGTC	55764
rs7637539	snp	A/G	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129470592	tttgtttgttttgag[A/G]cagagtctcactctg	55764
rs7639790	snp	A/G	0.463559	0.129972	intron-variant	IFT122	GRCh38.p7	3:129446578	atcaacctataagct[A/G]gaagccccctgcttc	55764
rs7640313	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471316	AGCAGATAATGAAGT[A/G]TTTTCTCAGTTTCCC	55764
rs7640391	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471332	TTTTCTCAGTTTCCC[A/G]TGGCTGATTTCCTAA	55764
rs9819604	snp	G/T	0.492287	0.0616198	intron-variant	IFT122	GRCh38.p7	3:129487953	GAGGCAGAGTGGGGA[G/T]GGGCAAAGGCATTCC	55764
rs9821282	snp	A/G	0.498253	0.0295011	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442145	AAACATTTGCTGGCC[A/G]AATGCAGCCTGATTT	55764
rs9824242	snp	A/G	0.29046	0.246704	intron-variant	IFT122	GRCh38.p7	3:129485194	ACTTGGCGCCTTGGC[A/G]TAAATTCCTAGAAAT	55764
rs9836202	snp	C/T	0.00943254	0.0680242	intron-variant	IFT122	GRCh38.p7	3:129515606	CTTCCTACGGTGAGT[C/T]CCTGCATCCTGAGCA	55764
rs9840794	snp	A/G	0.0349115	0.127424	intron-variant	IFT122	GRCh38.p7	3:129491860	TCCCAAGGAGGCACC[A/G]CCACAGACTGTGGCA	55764
rs9845069	snp	A/T	0.0596104	0.162024	intron-variant	IFT122	GRCh38.p7	3:129513290	TTGTCCCTGTTCTTT[A/T]CTAAATCTCACTGTA	55764
rs9845703	snp	A/G	0.0614824	0.164198	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457629	gagatgttgaccaaa[A/G]ggtagtttcagtcag	55764
rs9855705	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129517272	acattgctcctgcac[A/G]cacacacacacacac	55764
rs9855711	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129517274	attgctcctgcacac[A/G]cacacacacacacac	55764
rs9857517	snp	A/G	0.0733688	0.176922	intron-variant	IFT122	GRCh38.p7	3:129447434	aatgtctgggttaag[A/G]taaaggattgtggag	55764
rs9862434	snp	A/G	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129485210	taaattcctagaaat[A/G]aaattgctgggtcaa	55764
rs9864409	snp	A/G	0.0360663	0.129354	intron-variant	IFT122	GRCh38.p7	3:129473585	ctgacatctctgtgc[A/G]gttctttagctgtag	55764
rs9865030	snp	C/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129501361	TTTGGGGATATGGAA[C/G]AGGCTGGTTAATGAT	55764
rs9865445	snp	C/T	0.0360663	0.129354	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457730	aaactggcacaggaa[C/T]agttttttttttttt	55764
rs9865481	snp	C/T	0.463451	0.130149	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457798	tggagtgcagtggcg[C/T]gatctcggctcactg	55764
rs9871967	snp	A/G	0.299664	0.245017	intron-variant	IFT122	GRCh38.p7	3:129490335	GGCTCACCAGCTTGG[A/G]TATAGTGGTTCCTAG	55764
rs9873614	snp	C/T	0.279726	0.248226	intron-variant	IFT122	GRCh38.p7	3:129499054	GCCCTAGGCCTGATC[C/T]CTGAGCCTCCAGGAC	55764
rs9877785	snp	A/G	0.0337553	0.125452	intron-variant	IFT122	GRCh38.p7	3:129491659	TCCCTCTGTGGTACC[A/G]GGGGCTCTGGGTCCC	55764
rs9990401	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129500132	ATGTCACCTCTTGAC[C/T]GACAAGGGAACCAAT	55764
rs10470431	snp	A/G	0.499776	0.0105807	intron-variant	IFT122	GRCh38.p7	3:129448400	gggcacaaaagattg[A/G]ttggattggtgtttc	55764
rs10470432	snp	A/T	0.377385	0.215112	intron-variant	IFT122	GRCh38.p7	3:129448701	tttatttatttattt[A/T]ttttttttgagacgg	55764
rs10470433	snp	A/G	0.0618563	0.164627	intron-variant	IFT122	GRCh38.p7	3:129450802	ctcggcttactgcaa[A/G]ctccacctcccgggt	55764
rs10575597	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517269	ACACATTGCTCCTGC[-/CA]ACACACACACACACA	55764
rs10579071	in-del	-/GT	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129494708	TGTGTGTGTGTGTGT[-/GT]TGTTGGGGACATCAC	55764
rs10716502	in-del	-/T	0.266273	0.24947	intron-variant	IFT122	GRCh38.p7	3:129472726	ACATTAGACCTTTTG[-/T]TACTGTTCTCCAAGT	55764
rs10934884	snp	A/G	0.253544	0.249975	intron-variant	IFT122	GRCh38.p7	3:129467427	TCACTTAACATTATA[A/G]TGTGAACCCTTTCCA	55764
rs11293342	in-del	-/T	0.463774	0.129618	intron-variant	IFT122	GRCh38.p7	3:129473932	GTTTATTGTTGTTAC[-/T]TTGTGGGAAGATTGG	55764
rs11705823	snp	A/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129452789	gttgctgagttggaa[A/T]caacctgcaagaggt	55764
rs11711967	snp	A/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129496893	CAAAATTTTAACTCA[A/G]GATGAACCCTTAAGG	55764
rs11714005	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129498466	ACTAGGCGGGGACAG[C/T]GGCTGCTTTCCAAGC	55764
rs11718360	snp	G/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129493144	TTCTTAATTTCTGTG[G/T]ATCTCAGTGCTGTCT	55764
rs12107431	snp	C/T	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129443526	gccagatggactgca[C/T]gacaaggtctagagt	55764
rs12485319	snp	A/G	0.138207	0.223612	intron-variant	IFT122	GRCh38.p7	3:129452679	TGGGGTGGTCAGATC[A/G]taaagattttgattc	55764
rs12490492	snp	A/G			downstream-variant-500B	IFT122	GRCh38.p7	3:129521004	ACAGCTCCTTAAGCA[A/G]GGGGTTTCCGTTTGA	55764
rs12638398	snp	G/T	0.275464	0.2487	intron-variant	IFT122	GRCh38.p7	3:129494220	TTTGTTTGTTTGTTT[G/T]TTTTTTGCAGAGATA	55764
rs13066438	snp	A/G	0.0232847	0.105357	intron-variant	IFT122	GRCh38.p7	3:129471081	ATGCCAAGGATTAGA[A/G]TAAAGGTGCTGGGTA	55764
rs13070177	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129450946	aggatggtctcgatc[A/T]cctgacctcgtaatc	55764
rs13078698	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129501069	CATTCGTCAAGGTGG[A/C]CAACAGGGAGAGGAG	55764
rs13078699	snp	A/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129501071	TTCGTCAAGGTGGAC[A/G]ACAGGGAGAGGAGGG	55764
rs13079026	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129501105	TGGGGTGGGGCAGCA[A/C]TGAGACAGGATGGAT	55764
rs13090110	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450811	ctgcaagctccacct[C/T]ccgggttcacaccat	55764
rs13090114	snp	C/T	0.265453	0.249522	intron-variant	IFT122	GRCh38.p7	3:129450813	gcaagctccacctcc[C/T]gggttcacaccattc	55764
rs13090116	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129450819	tccacctcccgggtt[C/G]acaccattctcctgc	55764
rs13090150	snp	A/C/T	0.00597247	0.0543191	intron-variant	IFT122	GRCh38.p7	3:129450872	actacaggcgcctgc[A/C/T]gctacgctcagctaa	55764
rs13090435	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129450839	cattctcctgcctca[A/G]cctcctgagtagctg	55764
rs13091493	snp	C/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129468434	ctgcaacttccgcct[C/T]ccgggttctaagcga	55764
rs13091606	snp	C/T	0.0134861	0.0810011	intron-variant	IFT122	GRCh38.p7	3:129445655	aattacaagcacaga[C/T]tctagagtcagacct	55764
rs13433911	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129446889	GTTGTTTGTTTTTTG[A/T]GTGTTTTGTTTTGAG	55764
rs16859900	snp	C/T	0.266546	0.249452	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474600	AAGTGAGGGAAAGAG[C/T]ATTCCTGGCTGGGTC	55764
rs16859936	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129477278	AGGTCAGAAGATCAG[A/G]GTTCCCGGCCTCGCA	55764
rs17849712	snp	A/G/T	4.94466e-05	0.00497201	synonymous-codon	IFT122	GRCh38.p7	3:129488388	TTTAGATTTTGAAAC[A/G/T]GCAAAGAAGGTAAGC	55764
rs17852522	snp	A/G/T	1.65149e-05	0.00287353	intron-variant, synonymous-codon, missense	IFT122	GRCh38.p7	3:129467040	AGAACCAGAGGAAGA[A/G/T]GACGACAGTCCCAGG	55764
rs28405331	snp	A/G	0.463989	0.129263	intron-variant	IFT122	GRCh38.p7	3:129455388	ATGTTGGTCGGCCTG[A/G]TCTCAAACTCCTGAC	55764
rs28438812	snp	A/G	0.463881	0.12944	intron-variant	IFT122	GRCh38.p7	3:129451370	TCAAGCAATCCTCCC[A/G]CTTCAGCCTCCCAGA	55764
rs28442882	snp	C/G	0.0368353	0.130617	intron-variant	IFT122	GRCh38.p7	3:129453021	TTGGAGTTGCCCCCC[C/G]CACTGAGATGGAAAA	55764
rs28625331	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129513610	GATAGAACCTCTACC[C/G]TGAGCCTTACCCTGT	55764
rs34040345	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129443040	ATCTGCTGTAACTCT[-/C]CCATTCATGCCAGCT	55764
rs34159511	in-del	-/C			intron-variant, frameshift-variant	IFT122	GRCh38.p7	3:129519813	CTCTGGGAGGCGTGG[-/C]CCCTGGGAGGAGGGG	55764
rs34278576	in-del	-/CT	0.0232847	0.105357	intron-variant	IFT122	GRCh38.p7	3:129470603	TGAGACAGAGTCTCA[-/CT]CTGTCGCCTAGGCTG	55764
rs34328531	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129463064	TTTATTTTTCTTCTG[-/C]AAAGAATGATAGATT	55764
rs34334481	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129481982	TTTACCATGAACAAG[-/A]AAATGGGGCAATGAC	55764
rs34405470	snp	A/C	0.375	0.216506	intron-variant	IFT122	GRCh38.p7	3:129479253	AGAGACCCCATCTCC[A/C]CCAAAAAAAAAAAAA	55764
rs34568308	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129471682	AACCCCAACTTGTTT[-/G]GGGACAGTAAAATTG	55764
rs34574289	snp	A/G	0.257732	0.24988	intron-variant	IFT122	GRCh38.p7	3:129508395	AGTACCTAGTAGGCA[A/G]TGTACTGAGGGCTTC	55764
rs34712515	in-del	-/C			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507435	AAATATCCTCAAACT[-/C]CCCTGGCCTTATGCC	55764
rs34733354	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129469088	CAGCTGCAGCAGTGT[-/C]CCCAGCACCATAAGG	55764
rs34789317	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129501612	TTTTCTTGTCACTTT[-/C]CATTTGTAAGTGCTA	55764
rs34830400	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129461588	AACTTGGTGTTGCTG[-/C]CTTTGGGAAGCCTTC	55764
rs34834089	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129500807	ACACTGGAAGGGCCT[-/C]CCGATGCCAAACGGA	55764
rs34884786	in-del	-/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439579	CGCACAGGAAGAGCA[-/C]CTGGGCTCCAGACCC	55764
rs34971755	in-del	-/G	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129487940	TAGGTATTTTCCAGA[-/G]GCAGAGTGGGGAGGG	55764
rs35081517	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129443097	CACATGTCCACATGT[-/C]CTTTATAGGTGTTAT	55764
rs35323298	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129488488	CACGGAGAGGCCATA[-/G]GACTGCAGCAGTCTC	55764
rs35549328	snp	C/G	0.393987	0.204372	intron-variant	IFT122	GRCh38.p7	3:129517303	ACACACACACACACA[C/G]AGACTGCTCCTGCAC	55764
rs35584010	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129449214	AAGCCTTTATCAGAG[A/T]ACTGTTCTGTATTTC	55764
rs35642925	in-del	-/G	0.499776	0.0105807	intron-variant	IFT122	GRCh38.p7	3:129508808	TCAGGTGAATATTGC[-/G]GATGAGGCAAAATTT	55764
rs35688095	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129498422	CCATAGCAGCTGCCA[A/G]AAGGAAAGGTGTGTC	55764
rs35711969	snp	C/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129499837	CTTGCTGCTAGAAAA[C/G]CCTGATGTAACGCTG	55764
rs35761445	snp	C/G	0.498009	0.0314867	intron-variant	IFT122	GRCh38.p7	3:129517060	ACACACACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs35903154	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129442827	GGTCCTCCTGACCCT[-/C]CCTCCCCATCAGGCT	55764
rs35930684	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129488150	CAGGGCTGCTCCCCA[-/G]GCATGGGTAATCATC	55764
rs35961141	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129514307	CAAGCTGTGTTCCAG[-/C]CTGGGGCTCACTCCA	55764
rs36014236	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129449243	TCATCCAATCTAATA[A/G]GTCATTGATTATAAA	55764
rs36057864	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129511499	AAGAGGAGTTACTGG[-/C]CCTGCTGTAATCCTC	55764
rs36104554	snp	C/T	0.187053	0.241946	intron-variant	IFT122	GRCh38.p7	3:129505350	ATGGTAACCGTTGCC[C/T]TCTCTGGACACATTG	55764
rs36222038	snp	A/C	0.000669953	0.0182901	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440386	CTGCTCTTCGCGAAC[A/C]GCCCCGCTCCTCACC	55764
rs36222375	in-del	-/A			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442106	ACTCTGAAAAAAAAA[-/A]CAAAACACCGTGTGG	55764
rs36222376	snp	A/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440669	GCTTGAGCAGCTTCG[A/T]GCTGTCTCGTGGGTG	55764
rs55669321	snp	C/T	0.280256	0.248162	intron-variant	IFT122	GRCh38.p7	3:129449606	AATACCCTCAACAGT[C/T]GACCCTTTGAATAAT	55764
rs55704863	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129446157	AAGGCTTCCTCTGCA[A/G]ACAGTAACTTGGGTT	55764
rs55708833	snp	G/T	0.182933	0.240836	downstream-variant-500B	IFT122	GRCh38.p7	3:129520779	GTGGGGGAGCAGGGG[G/T]TTTTTTTGTTTATTT	55764
rs55728317	snp	A/G	0.175254	0.238565	intron-variant	IFT122	GRCh38.p7	3:129502048	TCCCCATGAGTGATG[A/G]GAGGGCTGCTCACCA	55764
rs55739764	snp	G/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129480933	TGGAGGGTACCTGTT[G/T]TCCCAGCTACTCAGG	55764
rs55744015	snp	C/T	0.277867	0.248442	intron-variant	IFT122	GRCh38.p7	3:129493334	GGCCAGCCCTTGTGC[C/T]GAGCTCAGTGGGCAC	55764
rs55752712	snp	C/T	0.463989	0.129263	intron-variant	IFT122	GRCh38.p7	3:129454210	GTCTCTTCACTTTAG[C/T]CCTGCATAAAGACAT	55764
rs55829132	snp	C/T	0.175254	0.238565	intron-variant	IFT122	GRCh38.p7	3:129518639	TGTCCTGGGCCTCCC[C/T]GCAGGACCCCTGCTG	55764
rs55860024	snp	C/T	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129463745	TGGTTTAGGCCCCTG[C/T]ATTTCCTTTTTTCTT	55764
rs55893186	snp	C/T	0.149999	0.229128	downstream-variant-500B	IFT122	GRCh38.p7	3:129520648	TACATTTTAGCAAAT[C/T]ATCTTATTGTCTGCA	55764
rs55893842	snp	C/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129489317	ACCTCAGGCCAGCCA[C/G]TTTCCTTGGAGCCCC	55764
rs55901466	snp	A/G	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129462035	GCCTAATCCCTCTCA[A/G]TGTTCCAGTTCCCTT	55764
rs55904629	snp	A/G	0.181978	0.240568	intron-variant	IFT122	GRCh38.p7	3:129462037	CTAATCCCTCTCAGT[A/G]TTCCAGTTCCCTTAT	55764
rs55970407	in-del	-/AC			intron-variant	IFT122	GRCh38.p7	3:129442580	ACAAAAAACTAAACA[-/AC]AAAAAAAAAAAGACA	55764
rs55975101	snp	G/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129472143	GTTGTATTGAGTAAT[G/T]TCATATGTCTGATTT	55764
rs55991801	snp	C/G	0.282105	0.24793	intron-variant	IFT122	GRCh38.p7	3:129488466	AAGGCAGATGGGGAC[C/G]CAGGTGGCACGGAGA	55764
rs56006215	snp	C/T	0.151334	0.229706	intron-variant	IFT122	GRCh38.p7	3:129447581	GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT	55764
rs56038317	snp	C/T	0.277867	0.248442	intron-variant	IFT122	GRCh38.p7	3:129479473	ATCAAAGTTAGAACT[C/T]CAAGCGGTTTAGGGT	55764
rs56041525	snp	C/G	0.0205511	0.0992634	intron-variant	IFT122	GRCh38.p7	3:129491701	GCACCACTGGGTAGG[C/G]ATAGCTGTCCCCTGC	55764
rs56051082	snp	A/G	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129477673	GGTGGGCAGGGAGCG[A/G]CCAGAGGTGAGGTCA	55764
rs56097652	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129490747	TTGCCCTCTCAAGGC[A/G]CTTTAAGGAAACCCA	55764
rs56116340	in-del	-/TGTG	0	0	intron-variant	IFT122	GRCh38.p7	3:129465156	GTGTGTGTGTGTGTG[-/TGTG]GTGTGTGAGTGATGC	55764
rs56152674	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129493156	GTGTATCTCAGTGCT[A/G]TCTGGCTGTCTGTTA	55764
rs56170476	in-del	-/TGTGTGTG			intron-variant	IFT122	GRCh38.p7	3:129465154	GTGTGTGTGTGTGTG[-/TGTGTGTG]GTGTGTGAGTGATGC	55764
rs56175050	snp	A/G	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129463247	TCGCATGTGTAGATT[A/G]CCATCAGCGTGACAC	55764
rs56230936	snp	C/T	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129489635	ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	55764
rs56267326	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129483856	TCTCCACTCCTTGCA[-/A]CCTGTGTGACTGGGG	55764
rs56283608	snp	C/T	0.185788	0.241613	intron-variant	IFT122	GRCh38.p7	3:129450783	TGGAGTGCAGTGACG[C/T]GATCTCGGCTTACTG	55764
rs56292219	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129490628	CAGGCCCCTTTCCAC[A/G]AAGAAGATGGTTGGA	55764
rs56379561	snp	A/G	0.223365	0.248577	intron-variant	IFT122	GRCh38.p7	3:129467081	TGTGAGTGTGTCCCA[A/G]TGAGTGGGAACCCTT	55764
rs56381009	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129444789	CCTCCCAAAATGCTA[A/G]GATTATAGGCGTGAG	55764
rs56698322	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129478458	ATTATTTTTTAAAAA[-/A]TATTTTTCTTGAGAC	55764
rs56720009	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129465142	GTGTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG	55764
rs56742126	snp	A/G	0.213333	0.247296	intron-variant	IFT122	GRCh38.p7	3:129452376	ACTGTTATGGAAGAA[A/G]AAAAAGTAGAGCAGA	55764
rs56757509	snp	C/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129491795	CTGCTGTGATGCTGC[C/G]TGACCCCCCAGAGGG	55764
rs56769711	snp	A/G	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129444800	GCTAAGATTATAGGC[A/G]TGAGCCACCATGTCT	55764
rs56821646	snp	A/G	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129491616	CCAGAATCTGTCTTT[A/G]TACCCTCTCAGCTTT	55764
rs57081612	snp	A/G	0.2776	0.248472	intron-variant	IFT122	GRCh38.p7	3:129484172	TCTGAACCAGGAGGT[A/G]GCCAGAACAGAAATG	55764
rs57127731	snp	A/C	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129449595	TTAGAAGAGTTAATA[A/C]CCTCAACAGTTGACC	55764
rs57400559	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129464192	TTCTTGCTGTTCAGC[C/T]TCTAGGAGTATATCC	55764
rs57434974	in-del	-/GGAGGA			intron-variant	IFT122	GRCh38.p7	3:129455922	GGAGGAGGAGGAGGA[-/GGAGGA]AGAGGGATTGGTGAT	55764
rs57498333	snp	A/T	0.0618563	0.164627	intron-variant	IFT122	GRCh38.p7	3:129518443	TGCCTTCCTTGCAGC[A/T]CCCAGGTGCTGCCAC	55764
rs57593455	snp	A/C	0.0618563	0.164627	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438723	CCAGCCTGGAGAGCA[A/C]AGTGAGATCCTCGTC	55764
rs57641956	snp	A/C	0.0618563	0.164627	intron-variant	IFT122	GRCh38.p7	3:129518444	GCCTTCCTTGCAGCT[A/C]CCAGGTGCTGCCACC	55764
rs57677080	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129485317	CCATACAACTCAGCT[G/T]CAGGCTAGAGCCCAC	55764
rs57715025	snp	G/T	0.281313	0.248031	intron-variant	IFT122	GRCh38.p7	3:129494216	TTTGTTTGTTTGTTT[G/T]TTTTTTTTTTGCAGA	55764
rs57845910	in-del	-/CTGG			intron-variant	IFT122	GRCh38.p7	3:129487374	ATTGCCAGCTATTTG[-/CTGG]GACAGGTCATTTGTC	55764
rs57859367	snp	C/T	0.186421	0.24178	intron-variant	IFT122	GRCh38.p7	3:129498635	TGAAAGCACATTTAC[C/T]CTGAAAGCAAATGAG	55764
rs58259329	in-del	-/G	0.464096	0.129085	intron-variant	IFT122	GRCh38.p7	3:129487757	CCCACCACTGCCCAC[-/G]GGCTGTGCACGGCTT	55764
rs58403413	in-del	-/GTGT/GTGTGT	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129494685	TGTGTGTGTGTGTGT[-/GTGT/GTGTGT]TGTTGGGGACATCAC	55764
rs58408920	snp	C/T	0.277867	0.248442	intron-variant	IFT122	GRCh38.p7	3:129485343	CCCACTTCTTCTAAG[C/T]TGATGATACCCTCGA	55764
rs58459843	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129443658	TTGCTTTCAAATTGT[A/G]TATGACTATAATTAA	55764
rs58532641	snp	A/G/T	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129464560	TTATTTCAAACCAAG[A/G/T]CATCATCCTCACTAG	55764
rs58550262	in-del	-/C	0.231589	0.249321	intron-variant	IFT122	GRCh38.p7	3:129478266	AATTCCATTTGTGCT[-/C]CCCCCCCAGTGATAG	55764
rs58743495	snp	A/G	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129487302	TATGCACATATACAC[A/G]CGTGCATACATGTGG	55764
rs58976074	snp	A/T	0.45843	0.138046	intron-variant	IFT122	GRCh38.p7	3:129460450	TTTTTCTTTATTATT[A/T]TTTTTTTTTATGAAG	55764
rs59023143	in-del	-/GAGGC			intron-variant	IFT122	GRCh38.p7	3:129513890	CCCCAGAGCACAGGC[-/GAGGC]TGCCGCTCAGAAACT	55764
rs59068291	snp	C/T	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129461660	CTGGCAGAGACAGTG[C/T]AGTTGTCCTCACCTT	55764
rs59128281	snp	A/G	0.218331	0.256302	intron-variant	IFT122	GRCh38.p7	3:129514244	TCACCTCTCACAAGC[A/G]CACAGAGCCTTCCTC	55764
rs59180237	snp	C/T	0.2776	0.248472	intron-variant	IFT122	GRCh38.p7	3:129484155	GGACTCTGCACAAGC[C/T]CTCTGAACCAGGAGG	55764
rs59504187	snp	C/T	0.0618563	0.164627	intron-variant	IFT122	GRCh38.p7	3:129494682	TTTATCCTAGCTGTG[C/T]TAAGTGTGTGTGTGT	55764
rs59520593	snp	C/G	0.0102121	0.0707231	intron-variant	IFT122	GRCh38.p7	3:129514330	TCACTCCAAGGACAG[C/G]CAGTGCCAGCTCCTG	55764
rs59563417	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129489856	AAAAAAAAAAAAAAA[-/A]GAATTCAGAGGAGGG	55764
rs59912693	snp	C/T	0.000889152	0.0210662	intron-variant, missense	IFT122	GRCh38.p7	3:129466943	ATGCCGAGGATGTCA[C/T]TGTCAACAGATATAT	55764
rs59954110	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510142	CATAGCTCATGGCAG[C/T]CTCAAACTGCTGGAC	55764
rs59956424	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129449014	TCAGCTTGCCTATCT[A/G]TGTTTGCAGCTCGAT	55764
rs59968045	in-del	-/T/TT			intron-variant	IFT122	GRCh38.p7	3:129442248	AAGAGTTAATTTTTT[-/T/TT]AAATCTGTTTAATTC	55764
rs60015665	snp	C/T	0.157642	0.232314	intron-variant	IFT122	GRCh38.p7	3:129484659	ATTTCACCTCACATT[C/T]GGTTATGGCAGCCCC	55764
rs60031306	in-del	-/T	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129467299	AGAAAGTTCAACTTT[-/T]CTGATAAAACCCCAT	55764
rs60037525	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129454411	AAAAAAAAAAAAAAA[-/A]GACAAGTCATGTGAC	55764
rs60153317	in-del	-/A			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438722	CCAGCCTGGAGAGCA[-/A]CAGTGAGATCCTCGT	55764
rs60199476	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129501082	GGACAACAGGGAGAG[A/G]AGGGGGTTGGGGTGG	55764
rs60226688	snp	G/T	0.11963	0.213316	intron-variant	IFT122	GRCh38.p7	3:129487376	TGCCAGCTATTTGCT[G/T]GGACAGGTCATTTGT	55764
rs60681706	snp	A/G	0.0562102	0.157941	intron-variant	IFT122	GRCh38.p7	3:129492226	TTTTCCTTCTCAAGA[A/G]GGCATACTTGGGGTT	55764
rs60689714	in-del	-/G	0.182933	0.240836	intron-variant	IFT122	GRCh38.p7	3:129494214	TTTTGTTTGTTTGTT[-/G]TGTTTTTTTTTTGCA	55764
rs60925130	snp	A/C/G	0.295935	0.279777	intron-variant	IFT122	GRCh38.p7	3:129443092	ATAGGCCACATGTCC[A/C/G]CATGTCTTTATAGGT	55764
rs61060445	in-del	-/C	0.181978	0.240568	intron-variant	IFT122	GRCh38.p7	3:129442581	CAAAAAACTAAACAA[-/C]AAAAAAAAAAGACAG	55764
rs61164956	snp	C/T	0.117886	0.21224	intron-variant	IFT122	GRCh38.p7	3:129500667	GGTAAATAGAGATGG[C/T]GGGAAAGGATATGCA	55764
rs61207347	in-del	-/TTTTTTGTA			intron-variant	IFT122	GRCh38.p7	3:129446391	GGCTAATTTTTTGTA[-/TTTTTTGTA]GAGACGGGGTTTCAC	55764
rs61229044	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129443533	GGACTGCATGACAAG[A/G]TCTAGAGTCCTTTCC	55764
rs61357505	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473789	AGAGGGCTGCCCTCA[A/G]GCAAAAACCCTTAAA	55764
rs61439083	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129465488	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	55764
rs61557048	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129454557	GTGTGTGTGTGTGTG[-/TG]CATGTTTGAGTTCAA	55764
rs61672415	in-del	-/CC			intron-variant	IFT122	GRCh38.p7	3:129472045	TTTAGTCTGTGGTCC[-/CC]ACCCTGCTGAAACCC	55764
rs61694557	in-del	-/CCT			intron-variant	IFT122	GRCh38.p7	3:129509326	TCTTCGGCAACTTCT[-/CCT]GTAGTTGTGAGAGGA	55764
rs61740161	snp	A/G	0.143394	0.226131	missense	IFT122	GRCh38.p7	3:129495459	AGGAGAGGAAGAAGC[A/G]GGGAGAGACCAACAA	55764
rs61741773	snp	A/G	0.0052738	0.0510792	synonymous-codon	IFT122	GRCh38.p7	3:129506440	GCGACAGAGAGAAGC[A/G]GTCCAGGTGCTGGAG	55764
rs61744218	snp	C/T	0.00572496	0.0531949	synonymous-codon	IFT122	GRCh38.p7	3:129502750	GGACAAGGCTGAGCG[C/T]GAGCCCCTGCTGCTG	55764
rs61744446	snp	C/T	0.0307617	0.120144	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476333	GGAAAGGATCGGGCA[C/T]TGAACTTTGACCCCT	55764
rs61744448	snp	A/C/T	0.000577977	0.01699	synonymous-codon, missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476327	CAGATTGGAAAGGAT[A/C/T]GGGCACTGAACTTTG	55764
rs61744639	snp	C/T	0.00946509	0.0681392	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478141	TCAGACATGCATTAC[C/T]GGGTAAAGGAGAAGA	55764
rs61746791	snp	A/C/T	1.64833e-05	0.00287078	missense	IFT122	GRCh38.p7	3:129483554	TTCTCGGGAGGAGGC[A/C/T]ACCTCAACATCAAAG	55764
rs62267561	snp	G/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129444469	GGGGCAGTGGTGCCT[G/T]TCCTGTCTACTACAT	55764
rs62267562	snp	A/G	0.0418186	0.138422	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503706	TCATGAGAAAAGGTG[A/G]GGCTAGGGACAGAGG	55764
rs62643908	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129516413	ACACATACAGAGACT[C/G]CCCCTGCACACACAC	55764
rs63122960	in-del	-/CA	0.464629	0.128197	intron-variant	IFT122	GRCh38.p7	3:129516099	CACAGACTGCTCCTG[-/CA]CACACACACACAGAC	55764
rs63683162	in-del	-/CTCAC			intron-variant	IFT122	GRCh38.p7	3:129504910	GTGTGAGGCATGGTC[-/CTCAC]TCTACTGAGAATAGA	55764
rs66484147	snp	A/G	0.281049	0.248064	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457129	TAATCCTCGTCTCTC[A/G]CCAGAGTAGGTGAAG	55764
rs66556397	snp	A/G	0.182296	0.240658	intron-variant	IFT122	GRCh38.p7	3:129495668	GGTATTCTCACGTGC[A/G]GTGTCCAAGTTATTT	55764
rs66573154	in-del	-/ACAC	0.0486741	0.148216	intron-variant	IFT122	GRCh38.p7	3:129517195	ACAGAGACTGCCCCT[-/ACAC]ACACACACAGACTGC	55764
rs66586915	snp	A/G	0.181978	0.240568	intron-variant	IFT122	GRCh38.p7	3:129460534	CAAACTGCTGGGATT[A/G]CAGGTGTGAGCCACT	55764
rs66679914	snp	A/G	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129468488	TAGCTGGGATTACAG[A/G]CACGCGACACCACGC	55764
rs66725762	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129453332	CAGCAACTGAGAGTG[A/G]CAATGGGGAAGGGAG	55764
rs66756682	snp	C/T	0.281313	0.248031	intron-variant	IFT122	GRCh38.p7	3:129459066	CTATTGGGGATCTGC[C/T]GTGTTCTTCCCCTGT	55764
rs66895088	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129448223	AATGGAAAACTAGGA[C/T]ACGGACACACCAGAG	55764
rs66896023	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129455164	TTTCTCCTTTAAGTT[C/T]ATTAAGTTTTTTTTG	55764
rs67042620	snp	A/G	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129448564	TTCTTTACTGTACAC[A/G]TGGTGACAAATTAAA	55764
rs67070415	snp	A/G	0.277334	0.248501	intron-variant	IFT122	GRCh38.p7	3:129483185	ATAAAAGATTTAGTC[A/G]TTATAAAAGATCCTA	55764
rs67239925	snp	A/G	0.281049	0.248064	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475151	GCCACAGAGTGTGAC[A/G]TTTCTCTGTGGCCAA	55764
rs67320575	snp	C/G	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129468113	GGTCATCTGCAGGCT[C/G]CCTCATTAACATCCC	55764
rs67544893	snp	A/G	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129493974	ATATCGACTGCCTGC[A/G]GACTTATTTGCACAC	55764
rs67622020	snp	A/G	0.281049	0.248064	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475971	ACTATAGGAAGAACT[A/G]TATTTGCAGAGGGAG	55764
rs67628805	snp	C/T	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129469832	TCAGGAAAGCCCTTT[C/T]ATAAAGGAGCTGCTG	55764
rs67655097	in-del	-/GCTG	0.17654	0.238964	intron-variant	IFT122	GRCh38.p7	3:129487373	TATTGCCAGCTATTT[-/GCTG]GGACAGGTCATTTGT	55764
rs67688838	snp	G/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129493981	CTGCCTGCAGACTTA[G/T]TTGCACACATCTGGG	55764
rs67787754	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129453918	CAGAGTTCTGTGAGT[C/T]TGAGCTGGTTATTGA	55764
rs67805751	snp	C/T	0.281313	0.248031	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475952	AGCTGAGGGAACCCA[C/T]TGAACTATAGGAAGA	55764
rs67904005	snp	A/G	0.182296	0.240658	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475675	AATTTTTTGCCAGGC[A/G]TGGTGGCACTCACCT	55764
rs67970798	snp	A/G	0.278664	0.248351	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438742	GAGATCCTCGTCTTT[A/G]CAAAAAATGAAAAAA	55764
rs68035274	in-del	-/AGGCG/GGCGG			intron-variant	IFT122	GRCh38.p7	3:129513887	GGGCCCCAGAGCACA[-/AGGCG/GGCGG]GGCTGCCGCTCAGAA	55764
rs68071362	snp	C/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129454857	GTCACACACATCTCA[C/T]TTGATGCTTCCAACA	55764
rs68095952	in-del	-/CTTC	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129459757	CTCCCTCCCTCCCTT[-/CTTC]CTTCCTTCCTTCCTT	55764
rs68126204	snp	C/T	0.2776	0.248472	intron-variant	IFT122	GRCh38.p7	3:129484778	GGTAAATGTTCTTAT[C/T]CTGCATGGCAAAATT	55764
rs68155216	snp	C/T	0.288386	0.247035	intron-variant	IFT122	GRCh38.p7	3:129499125	TTCCCTGCCTCAGAT[C/T]CCCCCATGGCCTCCT	55764
rs68181680	snp	C/T	0.182614	0.240747	intron-variant	IFT122	GRCh38.p7	3:129472991	CCTTAATCATAGTTA[C/T]AATAACTGTTTTAAA	55764
rs71255450	snp	C/T	0.0244538	0.107838	intron-variant	IFT122	GRCh38.p7	3:129498895	TAAAAGCTGCCTCAA[C/T]TCTGGCAAACTCCCA	55764
rs71255451	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129498933	ATTTTGGGTAACTAC[C/T]CTGAAAAGAGGTGGT	55764
rs71255452	snp	A/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129498982	ACACATTGTAGGGCC[A/T]GCCCAGAGAAGCTGG	55764
rs71255453	snp	A/G/T	0.00677024	0.0578401	intron-variant	IFT122	GRCh38.p7	3:129499005	GAAGCTGGGCATACC[A/G/T]CTTCAGAGGTATGCT	55764
rs71333614	snp	A/C	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129445953	ATTCAGAGGCCCCCC[A/C]ACCATCTGAATGGAT	55764
rs71333615	snp	C/T	1.64751e-05	0.00287007	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476746	CAAGGACCGCTATGC[C/T]TACAGGGATAGCATG	55764
rs71333616	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129493377	GAGAGAGGCTGACAG[A/G]AGCTCACAGCCTGCT	55764
rs71333617	snp	C/T	0.0174175	0.0916809	intron-variant	IFT122	GRCh38.p7	3:129499213	CCCTAACCATTCAGC[C/T]GAGAAGCAACTAACC	55764
rs71333618	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129501079	GGTGGACAACAGGGA[A/G]AGGAGGGGGTTGGGG	55764
rs71333619	snp	G/T	0.0499816	0.149975	intron-variant	IFT122	GRCh38.p7	3:129506575	ATCAGCCAGACCACT[G/T]TTTTCCCAAGCCCCA	55764
rs71333620	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129516034	CTGCACACACACACA[C/T]ACAGAAACTGCCCCT	55764
rs71333621	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129516040	ACACACACACACAGA[A/G]ACTGCCCCTGCACAC	55764
rs71931598	in-del	-/GT	0.433963	0.169285	intron-variant	IFT122	GRCh38.p7	3:129494686	TCCTAGCTGTGCTAA[-/GT]GTGTGTGTGTGTGTG	55764
rs72010084	in-del	-/A			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438752	TCTTTGCAAAAAATG[-/A]AAAAAAAAAACCCAA	55764
rs72152726	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129494697	CTAAGTGTGTGTGTG[-/TG]TGTGTGTGTGTTGTT	55764
rs72400649	in-del	-/GTGTGTGTGT			intron-variant	IFT122	GRCh38.p7	3:129465115	TGTACATGTATATGA[-/GTGTGTGTGT]GTGTGTGTGTGTGTG	55764
rs72407739	in-del	-/AGC	0.45889	0.13735	intron-variant	IFT122	GRCh38.p7	3:129499421	TCAGCCTCACTCTGA[-/AGC]ATGTGGTATCACCCA	55764
rs72983881	snp	C/T	0.0498117	0.149749	intron-variant	IFT122	GRCh38.p7	3:129486911	CTATGCCTGCTGCCC[C/T]GCTAAAGGGAGCATT	55764
rs72983886	snp	G/T	0.114036	0.209795	intron-variant	IFT122	GRCh38.p7	3:129487551	CCCCATCTTGTAGGA[G/T]GGCATCTGTCCCCAG	55764
rs72983902	snp	G/T	0.112631	0.208878	intron-variant	IFT122	GRCh38.p7	3:129492870	GTTCCCCAGGCTCAA[G/T]CGCAGTGGCACGATC	55764
rs72985926	snp	A/C	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129502006	GCCTGACCAGAGAGA[A/C]CAAGCGCATTCTATC	55764
rs72985998	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129513213	GGCCTGTGCAGCCAG[A/G]TACTGGATCATTACC	55764
rs72986971	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438942	TCATCTCAAAAAAAA[A/C]CCCACTAAACTAAAA	55764
rs72986983	snp	A/T	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129444371	TGATAATCATCCTTG[A/T]TCCAGCTTCTTTATC	55764
rs72986984	snp	A/G	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129445595	GATAACAGATTTGAC[A/G]TACTTGGCAGTAATT	55764
rs72986991	snp	A/C/T	0.126963	0.217802	intron-variant	IFT122	GRCh38.p7	3:129448247	ACCAGAGTGAGGTTA[A/C/T]GAGTAGAAGTTTAAC	55764
rs72987000	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129451691	GGTTCTCAAGGATTG[A/G]TAGTATATTCCTGGT	55764
rs72987906	snp	C/T	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129517893	GTCTGTGCATAGCTC[C/T]TGCATAGCCAACATG	55764
rs72988803	snp	C/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129454379	GGCCTGGGTGACAGA[C/G]CTAGACTCTGTCTCT	55764
rs72988811	snp	A/G	0.126219	0.217206	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457535	TCTACATCTGGCTAA[A/G]CTCTGCTCATCCTTT	55764
rs72988814	snp	A/C	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129459996	TTGAACTCCTGGGCT[A/C]AAGCAGTCCTCTCAA	55764
rs72988820	snp	C/G	0.181978	0.240568	intron-variant	IFT122	GRCh38.p7	3:129464059	TTACGTTCCTCATCT[C/G]ACAGATAGGGATAAA	55764
rs72988829	snp	A/C	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129467831	ATCCCACCCTGAGGT[A/C]ATGGGGGCTGGGAAG	55764
rs72988839	snp	A/G	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129471360	TAAAACTCTCATTTT[A/G]ATTAACTATCATCTA	55764
rs72988840	snp	C/T	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129471470	GTACGAGGCACTGGA[C/T]GTGGGTACTGAAGAC	55764
rs72988841	snp	C/T	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129472474	CTGGCCTACTTCTGA[C/T]TTTAAGTGGAAAGAT	55764
rs72988844	snp	A/C	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129473697	TCTTACTTTGCTTCT[A/C]TTTTCTGGGATTTCC	55764
rs72988847	snp	C/G	0.122064	0.214785	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476143	ATGAGTAGGGAGATG[C/G]AGAGGCAGAGAGGCC	55764
rs72988851	snp	C/T	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129477704	GTTACTTAGGCAGGC[C/T]TCTGATCACCGGGGG	55764
rs72988856	snp	G/T	0.0156448	0.0870498	intron-variant	IFT122	GRCh38.p7	3:129479951	CACGTCTCCTGTCAG[G/T]CTGATAATCTGCATG	55764
rs72988866	snp	C/T	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129484431	CTTAGCGCTTTTCTA[C/T]GTGTATATATAATAT	55764
rs73202295	snp	A/C	0.186357	0.241764	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438761	AAAATGAAAAAAAAA[A/C]CCCAAAAAAACAAAA	55764
rs73202302	snp	A/G	0.201727	0.245295	intron-variant	IFT122	GRCh38.p7	3:129454559	TGTGTGTGTGTGTGC[A/G]TGTTTGAGTTCAAGT	55764
rs73204207	snp	C/T	0.136847	0.222927	intron-variant	IFT122	GRCh38.p7	3:129460025	AAAGTACTGGGATTA[C/T]AGATACGAGCCACTG	55764
rs73204209	snp	A/T	0.181022	0.240296	intron-variant	IFT122	GRCh38.p7	3:129472333	TAATTAAAAAAAAAA[A/T]TTTTTTTTTTTTGGT	55764
rs73204210	snp	G/T	0.151001	0.229563	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476097	GGAGGTGCCACTGAC[G/T]CCAGGAGCTGAGGTT	55764
rs73204211	snp	A/G	0.151001	0.229563	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476128	TGGGCTGTGTAGAGG[A/G]TGAGTAGGGAGATGC	55764
rs73204212	snp	C/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129476945	TCTGTGTCTTGTTTT[C/T]TTTTTTTTTTTTTTT	55764
rs73204213	snp	A/C	0.151001	0.229563	intron-variant	IFT122	GRCh38.p7	3:129477145	ATGGGTCTTCGTGGA[A/C]CTTTATCCTTTCTGG	55764
rs73204214	snp	A/T	0.151001	0.229563	intron-variant	IFT122	GRCh38.p7	3:129477552	CAAAGCCCCTTGGGC[A/T]GCTTCACAGTGTCCC	55764
rs73204217	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129479625	GCCTTGCATGGAGTC[G/T]TGGATTAACGATGCC	55764
rs73204230	snp	C/T	0.286317	0.247348	missense	IFT122	GRCh38.p7	3:129495515	TCCTACCAGGGGAAG[C/T]TCCATGAGGCCGCCA	55764
rs73204231	snp	C/T	0.206015	0.2461	synonymous-codon	IFT122	GRCh38.p7	3:129495526	GAAGTTCCATGAGGC[C/T]GCCAAACTGTACAAG	55764
rs73204237	snp	A/C/T			intron-variant	IFT122	GRCh38.p7	3:129509944	GTTTTGAGGATTAGA[A/C/T]GAGTTAATATTGGAA	55764
rs73204238	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129514709	CCATGCCAGCTCCCC[C/T]GTGCTTCCCTGTCCA	55764
rs73204240	snp	C/T	0.0310518	0.120672	intron-variant	IFT122	GRCh38.p7	3:129518473	CCCCCAGGGGCCACA[C/T]TGGGAGGAGGGAAGC	55764
rs73865442	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439183	AAAATAATTTTGAGG[A/T]GCTGGATGGATCTTA	55764
rs73865443	snp	C/T	0.216349	0.247725	intron-variant	IFT122	GRCh38.p7	3:129442413	GTAGATGTATTCATA[C/T]GTGAATGAATGATGA	55764
rs73865444	snp	A/C	0.0663309	0.169604	intron-variant	IFT122	GRCh38.p7	3:129452966	TGGATATGGGCTATG[A/C]AGAAAAAGGAGTCAA	55764
rs73865445	snp	A/G	0.213937	0.247385	intron-variant	IFT122	GRCh38.p7	3:129468870	CCTGCAGGAGAACCT[A/G]TTTTTAGGTGTTAAT	55764
rs73865461	snp	A/G	0.0256215	0.110247	intron-variant	IFT122	GRCh38.p7	3:129471087	AGGATTAGAGTAAAG[A/G]TGCTGGGTACAGATT	55764
rs73865462	snp	A/G	0.02016	0.0983543	intron-variant	IFT122	GRCh38.p7	3:129487514	CGTTAGGAACTATTC[A/G]TGGGCACTCACAGCA	55764
rs73865463	snp	A/G	0.0228947	0.104514	intron-variant	IFT122	GRCh38.p7	3:129500986	AGAACCAAGTGGCCC[A/G]TCCCAGGGTGTTGGG	55764
rs73865464	snp	C/T	0.0244538	0.107838	intron-variant	IFT122	GRCh38.p7	3:129501840	GTTATTTTTAGATGC[C/T]ATTATTATTCTAAGT	55764
rs73865465	snp	C/T	0.0232847	0.105357	intron-variant	IFT122	GRCh38.p7	3:129504715	TGCAGTGTATCTTCC[C/T]GTTTAATCCTCGCAA	55764
rs73865466	snp	C/T	0.078151	0.181571	intron-variant	IFT122	GRCh38.p7	3:129511761	CTCCGCATGTGTGCT[C/T]GTTTGGTGGCACATC	55764
rs74323027	snp	G/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129497296	AAATGCCTGGCCTTG[G/T]TGCCCCAGAGCTGGT	55764
rs74346467	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129449450	GGATAGTAATTTCCC[A/T]GAGGGGAGGGAGGGA	55764
rs74486546	snp	A/G	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129515164	TAGTCCACGTGCTCC[A/G]CACGGTGCCCGGAGC	55764
rs74498035	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129500926	AGTGCAGTAGAGCAG[A/G]AGGGAACTTGGTAGC	55764
rs74643388	snp	G/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129501967	CCCTTTCTCCTGGGA[G/T]AGTTAGTTTGACTCC	55764
rs74664495	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129497713	TGATCACTATTCCAA[A/G]GAGGTTGGTTCCTTT	55764
rs74719990	snp	C/G/T	0.281839	0.255184	intron-variant	IFT122	GRCh38.p7	3:129478272	ATTTGTGCTCCCCCC[C/G/T]CAGTGATAGGGTGCC	55764
rs74755699	snp	A/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129446965	TGACACATTCTTACT[A/T]TAGTCACCTGAACCA	55764
rs74816131	snp	G/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129455191	TTTGTTTTTTTTTTT[G/T]AGATGAAGTCTCGCT	55764
rs74816873	snp	A/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438464	TGAATCTTCTTCATT[A/C]TTGATCCTCATGGTA	55764
rs74882653	snp	A/G	0.265727	0.249505	intron-variant	IFT122	GRCh38.p7	3:129446704	CCCTGACCACCTTGG[A/G]CACATGTTCTCAGGA	55764
rs74915976	snp	C/T	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129473141	CTCCATCCCTAAAAA[C/T]GAACAAACAAATTGG	55764
rs74932678	snp	G/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129450025	CCTTTTTTTTTTTTT[G/T]TGAGATTAAAAAGGC	55764
rs74972733	snp	A/G	0.0618563	0.164627	intron-variant	IFT122	GRCh38.p7	3:129479212	TGATTGCTTGAGGCT[A/G]GTAGTTCGAAAGCAG	55764
rs75005271	snp	C/T	0.0162398	0.0886349	intron-variant	IFT122	GRCh38.p7	3:129454909	GGGGACTCTTATCTC[C/T]GCTCAAAGATGAGAA	55764
rs75111418	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129458772	GGAGAAAACTTTTTT[C/T]TCTTAAATTGAACTT	55764
rs75352500	snp	A/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129455587	TAGCTAATTTTTTTT[A/T]AATTCTATTCCAGGC	55764
rs75470793	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440462	TGAGGGGGGCAGCGG[C/G]CTTGCTGCCTGGGCC	55764
rs75617961	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129449143	TAAATAATTTCTTTC[C/T]AGCTCCTGTATCACT	55764
rs75653847	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129469913	GCGGAGACACACTTG[A/G]TAGCAAAGAGCCCCT	55764
rs75660425	snp	A/G	0.00953873	0.0683987	intron-variant	IFT122	GRCh38.p7	3:129513411	ATTGGCCTCGCTAGA[A/G]GATTCCAGGCCCATT	55764
rs75763842	snp	G/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129468362	TTCTTTTTTTTTTTT[G/T]TGACAGAGTCTGGCT	55764
rs75844571	snp	A/G	0.192715	0.243348	intron-variant	IFT122	GRCh38.p7	3:129482940	CCAAATGTGAATCTT[A/G]TGTCTGAGCCTAGAA	55764
rs75995257	snp	C/T	0.26518	0.249539	intron-variant	IFT122	GRCh38.p7	3:129454802	ATGTCAGAGTGTGAC[C/T]CATCAGTAGTGGCAT	55764
rs76007598	snp	A/G	8.2618e-05	0.00642668	missense	IFT122	GRCh38.p7	3:129502718	CTCTCCAGGTTGATC[A/G]ACATCGCCCGCAAAC	55764
rs76040966	snp	C/T	0.0126979	0.078662	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441292	CTGTGTAAAGCATGC[C/T]GTCTCTCCTCATCTC	55764
rs76112337	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129514915	AAACCTCTGCCCTTT[C/T]TGGAACCAGGCTGTA	55764
rs76199871	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475228	CAAATTGAAACCACA[A/C]TGAGATAATTCGCAC	55764
rs76401157	snp	A/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438469	CTTCTTCATTCTTGA[A/T]CCTCATGGTAACCTT	55764
rs76523131	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129484018	GCAAAGCCGGGAGTC[C/T]GGCAGGGTGTGTGTG	55764
rs76558397	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438751	GTCTTTGCAAAAAAT[A/G]AAAAAAAAAACCCAA	55764
rs76572254	snp	C/T	0.00207353	0.032132	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504396	GTGGCTAGCAGAGAA[C/T]GATCGCTTTGAGGAA	55764
rs76687046	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129442590	TAAACAAAAAAAAAA[A/G]AGACAGTAGAACTAA	55764
rs76820675	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129497711	TTTGATCACTATTCC[A/G]AGGAGGTTGGTTCCT	55764
rs76831764	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129500521	TGTCGATGCCAACTA[C/T]GCGTGTAATGGTAGG	55764
rs76881473	snp	C/T	0.0057568	0.053341	synonymous-codon	IFT122	GRCh38.p7	3:129514530	TACCCTGACCATCCG[C/T]GCCAAGCCCTTCCAC	55764
rs76893037	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438934	GCGAGACCTCATCTC[A/C]AAAAAAAACCCACTA	55764
rs77037433	snp	A/G	0.0360663	0.129354	intron-variant	IFT122	GRCh38.p7	3:129505106	CCCTCTCTGTGTCAG[A/G]CCCTGGCTGAGCACT	55764
rs77132187	snp	A/G	0.267364	0.249396	intron-variant	IFT122	GRCh38.p7	3:129453023	GGAGTTGCCCCCCCC[A/G]CTGAGATGGAAAAGA	55764
rs77147461	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129487707	CATTGTGTCAGCAAA[C/T]GTAGACTGGGGTTCT	55764
rs77184436	snp	A/G	0.031235	0.121004	intron-variant	IFT122	GRCh38.p7	3:129514298	GCACCAGCACAAGCT[A/G]TGTTCCAGCCTGGGG	55764
rs77227277	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469170	ACTCTGCTTCATCCC[A/G]TAAGACTGATTGATG	55764
rs77393836	snp	A/C	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129473246	TCAAGGCTGCAGTGA[A/C]CTCTTACCACTGCAC	55764
rs77395911	snp	A/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129461118	GTCACTTGCAGAAGA[A/G]CATGTGGTCTAAAGT	55764
rs77434755	snp	G/T	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129472591	GTTCACTGAGCTTTT[G/T]GAATCTACACATTGA	55764
rs77493282	snp	A/G	0.0592355	0.161582	intron-variant	IFT122	GRCh38.p7	3:129519266	GGACCCTCAGCTAGC[A/G]CAGTGGTGGAGGAGG	55764
rs77532189	snp	C/T	0.0174175	0.0916809	intron-variant	IFT122	GRCh38.p7	3:129500806	CCACACTGGAAGGGC[C/T]TCCGATGCCAAACGG	55764
rs77599999	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129448121	TCTTCTTCATTAATC[C/T]TTTTCTGATCCTCTC	55764
rs77814002	snp	A/G	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129442622	AAAATCCTAGATGTC[A/G]AAGATTAGTCCTCCA	55764
rs77938079	snp	A/G	0.0150606	0.0854603	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520121	GTCCTGGCCCCAGGC[A/G]TAGGGCTGATGAGCA	55764
rs77979475	snp	C/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129446929	TAGTAACCTTAACAA[C/T]AGTCTGTTTTGACAG	55764
rs77984161	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129501695	ATGTTCTGCTTGCTT[C/T]CCAGATGTGGCTATA	55764
rs77988858	snp	G/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129500877	CAGACACCCCCTCAG[G/T]CAGGCAGGTAGAATG	55764
rs78079443	snp	G/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129455177	TTCATTAAGTTTTTT[G/T]TGTTTTTTTTTTTGA	55764
rs78116480	snp	A/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438468	TCTTCTTCATTCTTG[A/T]TCCTCATGGTAACCT	55764
rs78117023	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129466495	TTTTTTATTTTTATT[C/T]TTTTTTTTTTTTTTT	55764
rs78168161	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129471963	AGGTAAATACTGTTA[C/T]CATCACCATTTTACA	55764
rs78207749	snp	C/T	0.00292787	0.0381492	intron-variant	IFT122	GRCh38.p7	3:129492218	TGAAGCATTTTTCCT[C/T]CTCAAGAAGGCATAC	55764
rs78304877	snp	C/T	0.0162398	0.0886349	intron-variant	IFT122	GRCh38.p7	3:129517736	GAGATTGGAGAGGCC[C/T]ACATGGGACAGGGAC	55764
rs78331879	snp	A/C	0.109108	0.206518	intron-variant	IFT122	GRCh38.p7	3:129487216	TGGCTGGCCTAAAAC[A/C]AGGGCAAGGCCTTTC	55764
rs78445705	snp	C/T	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458306	TTACACTAGACTGAA[C/T]TTTATGAAAGTAGGG	55764
rs78590439	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129498416	TCCGCGCCATAGCAG[C/T]TGCCAGAAGGAAAGG	55764
rs78747241	snp	A/G	0.0704125	0.17392	intron-variant	IFT122	GRCh38.p7	3:129493018	GAGCAGGGTTTTCCC[A/G]TGTTGCCCAGGCTGG	55764
rs78750013	snp	A/T	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129451571	GTAGCTGGCTCTTTT[A/T]ATGGGCTAGTTTTAT	55764
rs78773292	snp	A/G	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129453311	CTTCAGTGAAATAGG[A/G]AGCAACAGCAACTGA	55764
rs78775900	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129509908	AAATAGGGATAACAG[C/T]ACTATGTACTTGATG	55764
rs78834324	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129443649	ACATGGCCATTGCTT[C/T]CAAATTGTGTATGAC	55764
rs78857239	snp	C/T	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129518822	CAGGATCCCTGGGCC[C/T]ATCCCCTCCGTGCCT	55764
rs78959157	snp	A/G	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129511723	ATGCCAGGAGCCAGG[A/G]AAATGGGTCAGCAGT	55764
rs79187669	snp	C/T	0.00162953	0.0284976	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476680	GGTCGGCTGCCAGGA[C/T]GGCACCATTTCCTTC	55764
rs79256663	snp	C/T	0.0482946	0.147699	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457607	TCATCTAAATTAGGT[C/T]CCCCAGGAGATGTTG	55764
rs79648507	snp	C/T	0.0693013	0.172766	intron-variant	IFT122	GRCh38.p7	3:129453654	AAATAATTATGTACA[C/T]TAACCTTGAATTGTT	55764
rs79698284	snp	C/T	0.265727	0.249505	intron-variant	IFT122	GRCh38.p7	3:129446680	TAAAATGTGTCAAAC[C/T]GAGCTGCACCCTGAC	55764
rs79893300	snp	A/C	0.0425829	0.139564	intron-variant	IFT122	GRCh38.p7	3:129510140	ATCATAGCTCATGGC[A/C]GCCTCAAACTGCTGG	55764
rs79918649	in-del	-/TT			intron-variant	IFT122	GRCh38.p7	3:129450025	CCTTTTTTTTTTTTT[-/TT]GAGATTAAAAAGGCA	55764
rs79976879	snp	A/T	0.0228947	0.104514	intron-variant	IFT122	GRCh38.p7	3:129448696	TTTTATTTATTTATT[A/T]ATTTTTTTTTTTTGA	55764
rs80015189	snp	C/T	0.266273	0.24947	intron-variant	IFT122	GRCh38.p7	3:129471874	AATAATAATAGCTAA[C/T]ATTTATTGAATTCCA	55764
rs80051311	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129494201	TCTAGTAAAACCTTT[C/T]TTGTTTGTTTGTTTG	55764
rs80154470	snp	G/T	0.29046	0.246704	intron-variant	IFT122	GRCh38.p7	3:129481413	TCCCTGCACAGAGCT[G/T]CTGGTGAAGGTGGTG	55764
rs80249455	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438752	TCTTTGCAAAAAATG[A/G]AAAAAAAAACCCAAA	55764
rs80329886	snp	C/T	0.265727	0.249505	intron-variant	IFT122	GRCh38.p7	3:129446514	GCCACCGCGCCCGGC[C/T]GACCCTAGGTCCTTA	55764
rs111162337	snp	C/G	0.275197	0.248727	intron-variant	IFT122	GRCh38.p7	3:129516804	TCCTGCACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs111162338	snp	C/G	0.0554779	0.157039	intron-variant	IFT122	GRCh38.p7	3:129516829	CTGCACACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs111162339	snp	C/G	0.187369	0.242028	intron-variant	IFT122	GRCh38.p7	3:129516858	ACACACACACACACA[C/G]AGGCTGCCCCTGCAC	55764
rs111162340	snp	A/G	0.28578	0.247426	intron-variant	IFT122	GRCh38.p7	3:129516861	CACACACACACAGAG[A/G]CTGCCCCTGCACACA	55764
rs111162341	snp	C/T	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129516911	CAGACACACAGAGAC[C/T]GCTCCTGCACACACA	55764
rs111163508	snp	C/G	0.499908	0.00678851	intron-variant	IFT122	GRCh38.p7	3:129516580	ACACACACACACACA[C/G]AGAGACTGCCCCTGC	55764
rs111163509	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129516663	ACACACACACACAGA[A/G]ACTGCCCCTGCACAC	55764
rs111211373	snp	A/G	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129516847	ACTGCCCCTGCACAC[A/G]CACACACACAGAGGC	55764
rs111211374	snp	C/G	0.0158469	0.0875917	intron-variant	IFT122	GRCh38.p7	3:129517006	ACACACACACACACA[C/G]AAACTGCCCCTGCAC	55764
rs111250570	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129487935	CCAAATAGGTATTTT[C/T]CAGAGGCAGAGTGGG	55764
rs111361839	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129491923	CTGATGCAACTGGGA[C/T]GTCTTTGCTGTTCTT	55764
rs111388105	in-del	-/A	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129449358	AGGTGAGAAAATGTG[-/A]AAAAAAAAATGTAAG	55764
rs111395823	snp	A/C	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129501642	ATAGTATCAGGTTAC[A/C]CTGAGGGTACTTGAG	55764
rs111406628	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440459	GTTTGAGGGGGGCAG[C/T]GGGCTTGCTGCCTGG	55764
rs111459031	snp	C/T	0.130262	0.21946	intron-variant	IFT122	GRCh38.p7	3:129459352	TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACCG	55764
rs111503076	snp	C/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129455329	AGGCACGCGCCACCA[C/T]GCCTAGCTAATTTTT	55764
rs111513637	snp	C/T	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129512733	CACCAGGCCTTCAGG[C/T]TTGGAACCTTGGGCA	55764
rs111525750	snp	C/G	0.5	0	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440117	GCCTTAGGGGCTCCA[C/G]TGCCACCATTGCTTT	55764
rs111536902	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129517739	ATTGGAGAGGCCCAC[A/G]TGGGACAGGGACAGG	55764
rs111583768	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129453462	CATGAAGGGCCCTCT[C/T]GAAGATTGTGATCAT	55764
rs111604972	snp	G/T	0.474634	0.109726	intron-variant	IFT122	GRCh38.p7	3:129450738	TTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTGGC	55764
rs111641979	in-del	-/T	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129509241	TCATGAGGCACCCAC[-/T]TTATCAAGCTTTTTC	55764
rs111642189	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129498166	GAGCCTTGAAGGAAG[C/T]TTTTAGACCCAGCTT	55764
rs111668739	snp	A/G/T	0.0033064	0.0405254	synonymous-codon	IFT122	GRCh38.p7	3:129517506	CTACCTGGAGGAAGG[A/G/T]ATCACTGATGAAGAA	55764
rs111682368	snp	A/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129489615	GAGGCCGAGGTGTGC[A/G]GATCACAAGGTCAGG	55764
rs111691596	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129452859	AGGGGGTGATGGTGG[C/T]TCAGACCTCTGTGGG	55764
rs111717774	snp	A/G	0.00294676	0.0382714	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478107	AATCCTCATCTATGA[A/G]TTGTATTCAGAGGAC	55764
rs111736800	snp	C/T	0.113685	0.209567	intron-variant	IFT122	GRCh38.p7	3:129455213	AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA	55764
rs111753761	snp	A/C	0	0	intron-variant	IFT122	GRCh38.p7	3:129492411	TAGCTGGGTGAGGCA[A/C]ATGGGTTCCGGATCT	55764
rs111808133	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129502290	AGAGTGCTGGGCCCA[A/G]TCTTGGGCTGGGTGC	55764
rs111839419	snp	A/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129492584	CTGATAGTGTTGGAG[A/G]AGTTTCCCAAATGCA	55764
rs111897163	snp	C/T	0.2776	0.248472	intron-variant	IFT122	GRCh38.p7	3:129470511	ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA	55764
rs111921975	snp	C/T	0.0174175	0.0916809	intron-variant	IFT122	GRCh38.p7	3:129497224	AGTGAGCCAAGATCA[C/T]GCCACTGCATTCCAG	55764
rs111965736	snp	C/T	0.181978	0.240568	intron-variant	IFT122	GRCh38.p7	3:129456568	CTTGAACCTGGGAGG[C/T]GGAGATTGCAGTGAG	55764
rs111975314	snp	C/T	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129492532	GCATCCTCCTGGTGG[C/T]GGATAGCTGGTCACC	55764
rs112016935	snp	C/G	0.281313	0.248031	intron-variant	IFT122	GRCh38.p7	3:129491299	GGCTCTGGAGCTGCT[C/G]CCTCCTCTAGGCACA	55764
rs112066509	snp	C/T	0.213568	0.247331	intron-variant	IFT122	GRCh38.p7	3:129483473	AGGATCCCCACTGTC[C/T]CTGTTCCCCAGGAAC	55764
rs112074075	snp	C/T	0.0101114	0.0703808	intron-variant	IFT122	GRCh38.p7	3:129459301	TTGTTTTGTTTTGTT[C/T]TGTTTTGAGACAGAG	55764
rs112077688	in-del	-/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129448698	TTATTTATTTATTTA[-/T]TTTTTTTTTTTGAGA	55764
rs112078967	snp	G/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129444259	CAAGGCTCAGAGGAA[G/T]AAAGCGTAAGAAACA	55764
rs112120558	snp	C/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129501953	TAGCCTGGGTAGAAC[C/T]CTTTCTCCTGGGAGA	55764
rs112208386	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129517117	CAGACACACAGAGAC[C/T]GCTCCTGCACACACA	55764
rs112283617	snp	A/C	0.18325	0.240924	intron-variant	IFT122	GRCh38.p7	3:129496825	CTAGAAGATTTCATA[A/C]CACATTCATACTGAG	55764
rs112285977	snp	A/G	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129497132	CCAAAAATGCAAAAA[A/G]TTAGCTGGTGCCTGT	55764
rs112300583	snp	C/T	0.0240643	0.107019	intron-variant	IFT122	GRCh38.p7	3:129448266	TAGAAGTTTAACAGG[C/T]GAAAGAAAGAGAAGA	55764
rs112301692	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443481	AGCAGGGGCTAGATG[A/G]CCATCTATAAGGAAT	55764
rs112375495	snp	A/G	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129473172	CCAGGGAGGTGGCAG[A/G]CACCCATTGTCCTAA	55764
rs112493154	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129517195	ACAGAGACTGCCCCT[A/G]CACACACACACAGAC	55764
rs112570141	in-del	-/CGCG	0.463559	0.129972	intron-variant	IFT122	GRCh38.p7	3:129465931	ACAGGCGTGAGCCAC[-/CGCG]CACGCCTGGCTAATT	55764
rs112587287	snp	C/G/T	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129513929	GGCCCTCGGGGAAGG[C/G/T]TGTGCAGACAGAGTG	55764
rs112615237	snp	A/G	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129513803	GGAGGGCCTGGGGGC[A/G]GCCAACATCGGAGGT	55764
rs112646713	snp	C/T	0.122411	0.214991	intron-variant	IFT122	GRCh38.p7	3:129479350	GCTGAGGCAGGAGAA[C/T]TGCTTTAGCCAGAAA	55764
rs112648818	snp	A/G	0.5	0	missense	IFT122	GRCh38.p7	3:129506424	CGTTCCACAAGGCTG[A/G]GCGACAGAGAGAAGC	55764
rs112663855	snp	C/G/T	0	0	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476691	AGGACGGCACCATTT[C/G/T]CTTCTACCAGCTTAT	55764
rs112672098	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129452130	GACAGTGAAGTTGCT[A/G]AGACTTCAGTTTGGT	55764
rs112696745	in-del	-/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129444955	GTAGGTAATAATACC[-/T]TTTTTTTGACATATG	55764
rs112741183	snp	A/G	1.6477e-05	0.00287024	intron-variant	IFT122	GRCh38.p7	3:129479939	TGAGTGCTCCCTCAC[A/G]TCTCCTGTCAGGCTG	55764
rs112803520	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129500840	TGCTTAGATTTGCCA[A/G]TAGTGAGTGACCACC	55764
rs112804857	in-del	-/TGGCTAT	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129451063	GTGATAGATGTCACA[-/TGGCTAT]TGGCTATCAAATACC	55764
rs112809330	snp	A/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129508551	ATTGCGGTTTCAGAC[A/T]GAATTTTAAATCATT	55764
rs112972053	snp	A/G	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129456419	CAAGGCGGGTGGATC[A/G]TGAGGTCAGGAGTTT	55764
rs113037071	snp	C/T	0	0	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441792	TGAATCTTTCATTTG[C/T]ACTTTTAATAGAGAT	55764
rs113067878	snp	C/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129486223	TGAGTGCCTGTCCCA[C/T]TCACGGGGCAGTCAG	55764
rs113102204	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511662	GGCAGCCTCTAGGTA[C/T]GAAGACCAATCACTA	55764
rs113103573	snp	A/C/G	4.94184e-05	0.00497063	missense	IFT122	GRCh38.p7	3:129500007	GCCGTGGAGATGTAC[A/C/G]TCTCAGCAGGAGAGC	55764
rs113204585	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129508763	AAAGTTGTTGAGATG[A/G]TTGAAGAAGTGGTAG	55764
rs113240695	snp	C/T			missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476438	AAGGATGGAGTGCGG[C/T]TTGGGACTGTTGGGG	55764
rs113240923	in-del	-/TG	0.280785	0.248097	intron-variant	IFT122	GRCh38.p7	3:129460780	GTGAAGGACTAAAAC[-/TG]GGGTTGAGACGCCTT	55764
rs113267763	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438216	TCGGATTAATCACTG[A/G]GTAGGGCTATTATAA	55764
rs113462870	snp	G/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129442341	AGACAGGTCAGTGGT[G/T]GTTGTTACTATGGAT	55764
rs113586834	snp	A/C	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129474104	CTATACAGGAAAGGA[A/C]ATTTGAATGTATTAA	55764
rs113588550	snp	A/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129506691	CTGCCTTGCAGTGGC[A/G]TAATCTGGTGTATCA	55764
rs113593468	snp	A/G			splice-donor-variant	IFT122	GRCh38.p7	3:129469418	CTGAGTGGAAAACAG[A/G]TATGTAGCCCTGTAC	55764
rs113605095	in-del	-/C	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129453014	GAAAGGTTGGAGTTG[-/C]CCCCCCCCACTGAGA	55764
rs113616544	snp	A/G	0.0162398	0.0886349	intron-variant	IFT122	GRCh38.p7	3:129444309	ACCACATAATGGTGA[A/G]GAAGCTGAAAAACTC	55764
rs113669277	snp	C/T	0.122064	0.214785	intron-variant	IFT122	GRCh38.p7	3:129489761	GGAGAATGGCGTGAA[C/T]CTGGGAGGCGGAGCG	55764
rs113694930	snp	A/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129497094	GAGACCAGCCTGGGC[A/G]ATATGGTGAAACCCT	55764
rs113695838	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129494782	AGTCAGACAGAACTG[C/T]GTCCAAATTCCAGCT	55764
rs113708792	snp	C/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129445392	GGCTCCATTTCCATT[C/T]AGTAGCACTTTATTT	55764
rs113709315	snp	A/G	0	0	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458395	GTAGGCTCCCAATAC[A/G]TCTTTGTTTACTCAG	55764
rs113724559	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129472267	CAAGGAATCTTCCCA[C/T]TTTGGCCTTCCAAGT	55764
rs113737110	snp	C/T	0.0115144	0.0749975	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504134	TTGCTGTTAATTGCC[C/T]TTTGTTTTCGAAGAG	55764
rs113757722	snp	A/G	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129488718	TATTAGCTGTTCTCT[A/G]TGGGAAGCACCTGAC	55764
rs113777977	snp	C/G	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129462624	ATAACATGTGCACAC[C/G]TCAAAATGTTTGGAG	55764
rs113802734	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129501199	CTTCAGGCTCAAGCA[C/T]GTGCACACACACGTG	55764
rs113804140	snp	C/G	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129504736	ATCCTCGCAACAGCC[C/G]TATGGTATAGCTACC	55764
rs113865558	snp	C/T	0.5	0	intron-variant	IFT122	GRCh38.p7	3:129447898	CACTTCCCGTCATGG[C/T]CTGAAACAGTCTCTC	55764
rs113871672	snp	C/T	3.74322e-05	0.00432605	synonymous-codon	IFT122	GRCh38.p7	3:129481544	GATCCTGAAGATCTT[C/T]GTGGACAATCTCTTT	55764
rs113872971	snp	C/T	0.0185938	0.0946107	intron-variant	IFT122	GRCh38.p7	3:129492337	GCCACAGCCTTGCTC[C/T]GGGGGCAGAGTGGCC	55764
rs114015618	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129496478	ATGAAGTGACTCATC[A/G]GCCATAACCTATTGG	55764
rs114016263	snp	A/G	0.00631002	0.0558139	intron-variant	IFT122	GRCh38.p7	3:129476833	GACCTTGGGAAGAGG[A/G]ACAGGTGGAAGCAGG	55764
rs114073367	snp	C/G	0.0228947	0.104514	intron-variant	IFT122	GRCh38.p7	3:129487942	GGTATTTTCCAGAGG[C/G]AGAGTGGGGAGGGGC	55764
rs114150455	snp	C/T	0.0146672	0.084371	intron-variant	IFT122	GRCh38.p7	3:129509289	CAAATGCCAAACAAC[C/T]GTAGAATGGTTGACA	55764
rs114222894	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129473428	ATTGTACTCAATATT[A/G]TGAGTAATATGTCAT	55764
rs114223346	snp	C/T	0.00993419	0.0697739	intron-variant	IFT122	GRCh38.p7	3:129500293	GGGAAGAGGAGACAC[C/T]GGGACATCACAGCTG	55764
rs114298924	snp	C/T	0.0447667	0.142756	intron-variant	IFT122	GRCh38.p7	3:129451899	TAGATAATCTGTATT[C/T]GTCTCTTTTGCCAGG	55764
rs114324056	snp	A/G	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129505026	ACAACAGCATCTGAA[A/G]TAGGAGTTAAAGCAA	55764
rs114328774	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129486111	CAGAGAGTATTTGTT[C/T]AGTGGGGTCTATTTT	55764
rs114354396	snp	A/G	0.0236746	0.106192	intron-variant	IFT122	GRCh38.p7	3:129453060	GTAGAGAAAAGTTAT[A/G]GTTGAAGATCAGAAA	55764
rs114357746	snp	A/C	0.00269798	0.0366294	synonymous-codon	IFT122	GRCh38.p7	3:129500042	CAAGGCCATCGAGAT[A/C]TGTGGTGACCATGGC	55764
rs114422006	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439192	TTGAGGAGCTGGATG[A/G]ATCTTATGAAATGAT	55764
rs114440105	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129508355	CACTGTATCTCCTCA[A/G]TCACCCAACAGATGT	55764
rs114519508	snp	G/T	0.0119091	0.0762411	intron-variant	IFT122	GRCh38.p7	3:129458805	AATTAAGTTGTGGGT[G/T]TGTGTGGTTGGTATA	55764
rs114535748	snp	C/T	0.0244538	0.107838	intron-variant	IFT122	GRCh38.p7	3:129494095	GAAAGAACCTGCCCA[C/T]GTTGACATGCACCTG	55764
rs114555128	snp	A/G	0.0543475	0.155628	intron-variant	IFT122	GRCh38.p7	3:129459088	TTCCCCTGTTCCTCT[A/G]CTAGTTGGTCCCTAT	55764
rs114602799	snp	C/G/T	0.0722614	0.17581	intron-variant	IFT122	GRCh38.p7	3:129514770	CCCGCTCACAGCCCC[C/G/T]GGCCCCGGCCTCAGC	55764
rs114658408	snp	C/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129501169	GGGGAAGGCTTTGTC[C/T]TCCCAGTCAGTGAGC	55764
rs114729257	snp	G/T	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129468358	GCTTTTCTTTTTTTT[G/T]TTTGTGACAGAGTCT	55764
rs114750085	snp	C/T	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129482506	CCCCTTACCAGGCTC[C/T]TCCTTGTTCTCAGCA	55764
rs114763710	snp	C/T	0.029116	0.117091	intron-variant	IFT122	GRCh38.p7	3:129484010	AGTGAGCAGCAAAGC[C/T]GGGAGTCCGGCAGGG	55764
rs114836712	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129513844	GAGAGCACAAAGGCT[C/T]GTCAGCCTCTGGCTG	55764
rs114963006	snp	A/G	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129449641	TGTGTCTGGCTTCTG[A/G]ACAAGAGGAAATCAG	55764
rs114972179	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505582	GGTTGTAGATGAGAA[C/T]GGAACAAAGGCCAGA	55764
rs115003691	snp	C/T	0.1609	0.233583	intron-variant	IFT122	GRCh38.p7	3:129488004	GGCGAGGCAGGCCTG[C/T]AGGTGGGAAGGAGGG	55764
rs115061281	snp	G/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129461401	GATTTTATCCTGAGA[G/T]AGTTAATACTACTTC	55764
rs115113244	snp	A/T	0.0138799	0.0821421	intron-variant	IFT122	GRCh38.p7	3:129507912	TCTGGGAAGAAAAAG[A/T]TTGAGTTTCTTTGAT	55764
rs115170621	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129509665	TTGAAATGATGTATA[A/G]CATAACCACATTTAA	55764
rs115206156	snp	A/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129476920	TTTTGCAAACCTGTT[A/T]GCCACTGGGTCTGTG	55764
rs115212090	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480508	AACTTTGAAAGTGAC[A/G]ATGTAGCTGCATTAG	55764
rs115328230	snp	A/G	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129491654	TCTGCTCCCTCTGTG[A/G]TACCAGGGGCTCTGG	55764
rs115378209	snp	G/T	0.0248432	0.108648	intron-variant	IFT122	GRCh38.p7	3:129442427	ACGTGAATGAATGAT[G/T]AATAAAGATTGGTTT	55764
rs115423509	snp	C/T	0.0182019	0.0936463	intron-variant	IFT122	GRCh38.p7	3:129518775	TCCATCACAAGTGCC[C/T]GCAGACCCCCAGCAG	55764
rs115426262	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514176	TATTAATGGAAACTA[C/T]GCTGTTTTTATCTTT	55764
rs115426559	snp	A/G	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129462652	GAGGAAGCGTTCTGG[A/G]CCAGGGGAAAGGCAA	55764
rs115558379	snp	C/T	0.00795532	0.062565	intron-variant, missense	IFT122	GRCh38.p7	3:129503537	AGAGAAATCCATCCC[C/T]GAGAGGATTAGGAGC	55764
rs115580670	snp	A/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129515003	TCCTTCTTTCACACA[A/T]CCTCCCTCAAGCTCA	55764
rs115657971	snp	A/G	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129483403	GGGATTCAGTCTTTA[A/G]GAGGGTATTGGGCTG	55764
rs115708303	snp	A/G	0.0162398	0.0886349	intron-variant	IFT122	GRCh38.p7	3:129481990	TGAACAAGAAATGGG[A/G]CAATGACTCTGAGAG	55764
rs115709424	snp	A/G	0.0360663	0.129354	intron-variant	IFT122	GRCh38.p7	3:129459888	CTTCCCAAATAGCTG[A/G]AACTGCAGGTGCACA	55764
rs115715082	snp	A/G	0.000100103	0.00707402	missense	IFT122	GRCh38.p7	3:129514393	GTTCACGGCAGGAAA[A/G]TACTCTTCACCTTGG	55764
rs115775972	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129462623	GATAACATGTGCACA[C/T]GTCAAAATGTTTGGA	55764
rs115832705	snp	C/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129493582	GGTGGAATTCAAGCC[C/T]AGTCTATTTCCTAAG	55764
rs115839555	snp	C/T	0.0271762	0.113356	intron-variant	IFT122	GRCh38.p7	3:129489939	CAGCAGGGAGGGAGA[C/T]GACAAATCCCTAGAA	55764
rs115840909	snp	C/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129485580	CCCATTACAAACCCA[C/T]GCACCACATCCACCA	55764
rs115887933	snp	A/C	0.00755907	0.0610114	intron-variant	IFT122	GRCh38.p7	3:129445274	GAGGTTGCTGTGAGC[A/C]AAGATCCTGCTACTG	55764
rs115948527	snp	C/G	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129451135	ACAGGGTTGTGCTCT[C/G]TTGCCCAAGCTGGTG	55764
rs115967845	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505478	GCTGAAGTATCTGCA[C/T]GTTTGGGCAAAACAC	55764
rs116017407	snp	C/T	0.0142736	0.0832652	intron-variant	IFT122	GRCh38.p7	3:129491817	CCCAGAGGGTCAGAC[C/T]GGCTTGTTCTTCTTT	55764
rs116046381	snp	G/T	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129468360	TTTTCTTTTTTTTTT[G/T]TGTGACAGAGTCTGG	55764
rs116070998	snp	A/T	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129512161	GATGAGACAGTGGCT[A/T]TATGGCGCTCAGCAC	55764
rs116079051	snp	C/T	0.0185938	0.0946107	intron-variant	IFT122	GRCh38.p7	3:129448186	TCTGGGGTAAATATC[C/T]GAGATTTGTTGTCTC	55764
rs116163066	snp	C/T	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129451356	TTGAACTCCTGGTTT[C/T]AAGCAATCCTCCCAC	55764
rs116196975	snp	A/C	0.00121835	0.0246514	missense, intron-variant	IFT122	GRCh38.p7	3:129460897	CTCCATCTTCCATTT[A/C]TGGGCCTCCACAAAA	55764
rs116231256	snp	C/G	0.0107246	0.0724382	intron-variant	IFT122	GRCh38.p7	3:129452274	TTATGGGGTGGTGGT[C/G]AGAAGTGAGGGAGGA	55764
rs116262080	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129453372	AGTTGAAGAGAAAGG[A/G]AAAAAGTGTAAAGTC	55764
rs116264845	snp	C/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129480030	GCAGGAAAAGGGCTT[C/T]TCTCCTCCATGGGTG	55764
rs116382230	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472526	TATTATTTAAGGTTC[C/T]TAAGCAATATTGGAA	55764
rs116413808	snp	C/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129479709	TTCTCCCCTTAGGGA[C/G]AGAAAGATCTCCTTG	55764
rs116415423	snp	C/G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462467	GTAGAGGTCCCTTAG[C/G/T]TAGTAAGTGGAGGAA	55764
rs116415793	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129497925	AAATTGTATGCTTTC[C/T]GGATAAGTGACATGT	55764
rs116477511	snp	C/T	0.0123036	0.0774623	intron-variant	IFT122	GRCh38.p7	3:129510749	TCAGACCAGCTGGGG[C/T]CCTGGCTCTTATCCC	55764
rs116507758	snp	A/G	0.0182019	0.0936463	intron-variant	IFT122	GRCh38.p7	3:129483805	GGCAGCTGTGAGGTC[A/G]TGGGAGGCAGTCTGG	55764
rs116514402	snp	C/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129505394	TCCCTGTTGGAGCCC[C/T]TCAACCGAAAGCCCT	55764
rs116562470	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440500	CTGAACCCCGGCCTG[A/G]GAGACTGCAGGGTCG	55764
rs116564681	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129510325	CATTTTTTGCCTCTT[A/G]GGAAAGTCTGGCAAG	55764
rs116573261	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129513542	GCTATGCCTGTGGGG[A/G]CTGAGCACCTGTACT	55764
rs116660716	snp	C/T	0.0217236	0.101931	intron-variant	IFT122	GRCh38.p7	3:129482529	TCTCAGCAGCAGAAT[C/T]GATGGGGGAGGGGTC	55764
rs116789074	snp	C/T	0.0236746	0.106192	intron-variant	IFT122	GRCh38.p7	3:129513495	GACCTCTGCTGCATG[C/T]GTCTCCGTCTTTCCC	55764
rs116819033	snp	C/T	0.00738591	0.0603192	synonymous-codon	IFT122	GRCh38.p7	3:129495553	CAAGAGGAGTGGGCA[C/T]GAGAACCTCGCGCTT	55764
rs116884970	snp	C/T	1.64732e-05	0.0028699	intron-variant	IFT122	GRCh38.p7	3:129460851	GATTTGTCATGTTTC[C/T]AGATCTTGGTCTGTG	55764
rs116912147	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129497141	CAAAAAATTAGCTGG[C/T]GCCTGTAGTCCCAGC	55764
rs116983337	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129454910	GGGACTCTTATCTCC[A/G]CTCAAAGATGAGAAA	55764
rs117212537	snp	C/T	0.0479149	0.147179	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503885	GGCTTAGGTGAGAAG[C/T]AGTCAGTGGGTCCAT	55764
rs117320718	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441214	AGCATTGTTGTGAAG[C/T]CTCTGTTCTGGCCAC	55764
rs117414351	snp	A/C	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129473967	ATGGGAACTAGTGAG[A/C]CATTTCCAGAAGCTG	55764
rs117517364	snp	G/T	0.0054394	0.0518663	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476323	TCCTCAGATTGGAAA[G/T]GATCGGGCACTGAAC	55764
rs117633949	snp	C/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129482741	TGATCTTAAGTTAGT[C/G]AGCCTCTCTGAGCCT	55764
rs117817067	snp	A/G	0.0115144	0.0749975	intron-variant	IFT122	GRCh38.p7	3:129494628	ACAAATACTCGAGCT[A/G]TAGACAAGCGAATGT	55764
rs117899459	snp	A/G	0.0788843	0.182262	intron-variant	IFT122	GRCh38.p7	3:129478602	GGCACATGCCACCAC[A/G]CCCAACTAATTTTTT	55764
rs117900894	snp	C/T	0.0111196	0.0737302	intron-variant	IFT122	GRCh38.p7	3:129487844	AGGAAGCTGAGACTC[C/T]TTCCCCTGGGGTGGG	55764
rs117956136	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129482731	CCTTACTGTGTGATC[C/T]TAAGTTAGTGAGCCT	55764
rs118029711	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482008	ATGACTCTGAGAGGG[G/T]TGTGACGTTGGCACT	55764
rs118077015	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495707	AGTGCTGCGGACAAA[A/G]ACTAGCAATGGTCTC	55764
rs118103988	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129471578	CATGGCCGAGGGCCA[C/T]AGGAAATATCTTGCA	55764
rs118174944	snp	A/G	0.0433465	0.140692	intron-variant	IFT122	GRCh38.p7	3:129451362	TCCTGGTTTCAAGCA[A/G]TCCTCCCACTTCAGC	55764
rs137865583	snp	A/C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482692	AGCCTTCAAGCTGAC[A/C/T]TGGGCTTGGGTCCTG	55764
rs137977115	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129506654	GCCCTGGGCTTGTTT[A/G]TTGGGTGTATTGTCC	55764
rs137984204	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474318	CTTAAGGAGAAACCA[C/G]TTCCCTAAAGTTATT	55764
rs138005939	in-del	-/AGCTGCAT			intron-variant	IFT122	GRCh38.p7	3:129453532	TCTCCAGCGATTTTG[-/AGCTGCAT]AGTTGTAGAGGCAGA	55764
rs138028750	snp	A/G	0.000135505	0.00823008	missense	IFT122	GRCh38.p7	3:129515551	AACAACCTGGGCAAC[A/G]TCTGCATCAACTGCC	55764
rs138083251	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129513121	ACCCAAGGCCTGAGA[A/G]CCTACCTTTGGGTTT	55764
rs138085257	snp	C/T	0.0287284	0.116357	intron-variant	IFT122	GRCh38.p7	3:129442636	CAAAGATTAGTCCTC[C/T]ACATCCAAATCAGCC	55764
rs138138714	snp	C/T	8.25512e-05	0.00642408	missense	IFT122	GRCh38.p7	3:129502727	TTGATCGACATCGCC[C/T]GCAAACTGGACAAGG	55764
rs138184580	snp	A/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129451277	CTAATTTTTATTTTT[A/T]TTTATTTTTATTTAT	55764
rs138184756	snp	C/T	0.0271762	0.113356	intron-variant	IFT122	GRCh38.p7	3:129495770	ACCCATCTACAGCCA[C/T]TGGTTGAAACTCACC	55764
rs138223055	snp	A/G	0.000827705	0.0203265	missense	IFT122	GRCh38.p7	3:129481594	AGGCCACAGCTGTGC[A/G]CTGCTTGGACATGAG	55764
rs138296643	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455511	AACCATGATATAAAA[C/G]TATGTAAGACATAGT	55764
rs138327589	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129460165	ACCAATCTCCCAAAC[G/T]CTTTTATCCTGCTAA	55764
rs138329739	snp	C/T	0.000115313	0.0075923	intron-variant, stop-gained	IFT122	GRCh38.p7	3:129466891	CTTACTGTCTACAGC[C/T]GATGGGAGAGTTTCT	55764
rs138334179	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129468623	TGCTGGAATTACAAG[C/T]GTGAGCCATCACGGG	55764
rs138482462	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492911	GCAGCATAGACCTCC[C/T]AGGCTCAAATGATCC	55764
rs138499161	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129498929	GTGTATTTTGGGTAA[C/G]TACTCTGAAAAGAGG	55764
rs138539494	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501345	AGTGGCCCAGCCAGG[A/T]TTTGGGGATATGGAA	55764
rs138542931	snp	A/G	0.0115144	0.0749975	intron-variant	IFT122	GRCh38.p7	3:129512860	CTGCCATCAAAGAGG[A/G]AGGTCACAAGTTAGG	55764
rs138555352	in-del	-/CAT	0.0260105	0.111035	intron-variant	IFT122	GRCh38.p7	3:129462930	TAGATTTTCAGAAAG[-/CAT]CATTGTTATTTTAAA	55764
rs138569201	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491745	TGCCAAGATGTATAG[A/G]CAGTCTCTCATCAGT	55764
rs138588238	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129479012	TGAGAGAAGGCTAGC[A/C]CAGCATCTTGGAAGT	55764
rs138643237	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129484440	TTTCTACGTGTATAT[A/G]TAATATATGCATAAT	55764
rs138715299	snp	G/T	0.000153988	0.00877328	missense	IFT122	GRCh38.p7	3:129500002	AAGCCGCCGTGGAGA[G/T]GTACATCTCAGCAGG	55764
rs138726986	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502413	TGGGAAAGCTCATGG[C/T]GTCATCTGGGTACCT	55764
rs138770833	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507047	GACAAGGCCACATGC[A/G]GGGGTGGGAAAAACA	55764
rs138793724	snp	A/G	0.00653679	0.0567957	synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461276	TCCTATTACTCATCA[A/G]CTGGCATCTTGTTCC	55764
rs138927447	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520791	GGGGTTTTTTTGTTT[A/G]TTTATTTTGATTTAA	55764
rs138944243	snp	C/T	0.112631	0.208878	intron-variant	IFT122	GRCh38.p7	3:129498484	CTGCTTTCCAAGCCC[C/T]TTCCCTTTGTCAGCT	55764
rs139008392	snp	C/T	6.58924e-05	0.0057395	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466995	GAAGTCAGCAGTGTA[C/T]AGTAGTCAGGGTAGT	55764
rs139058883	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464463	ACAGAACTAAATAGC[A/C]TTTTAAGTTTGATCC	55764
rs139079256	snp	C/T	9.97108e-05	0.00706013	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478018	TTTTCTTTGACAGTT[C/T]GGATTAAATGCAAAG	55764
rs139097887	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517840	CGTGTGGGTCTCCCA[C/T]CCTCCCCTGACCCCT	55764
rs139138308	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449883	CAGTATAAATGACAT[C/T]GCATTTAAGCCTGAT	55764
rs139145049	snp	A/G	0.000103701	0.00719999	missense	IFT122	GRCh38.p7	3:129483624	TTGTGGTCGGCTACA[A/G]TGGCTCCAAGATCTT	55764
rs139210547	snp	C/T	0.0107246	0.0724382	intron-variant	IFT122	GRCh38.p7	3:129469723	CCTAGGAGTTAAACC[C/T]AGGTTGGTTTGACTT	55764
rs139251443	in-del	-/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129466065	CCACCCACCTCAGCC[-/T]CCCAAAGTGCTGAGA	55764
rs139286035	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129509667	GAAATGATGTATAAC[A/G]TAACCACATTTAAGA	55764
rs139299979	snp	C/T	0.0138799	0.0821421	intron-variant	IFT122	GRCh38.p7	3:129487991	GGTGACATCCTATGG[C/T]GAGGCAGGCCTGTAG	55764
rs139319087	snp	C/T	0.00240321	0.0345808	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476767	GGATAGCATGACTGA[C/T]GTCATTGTGCAGCAC	55764
rs139327046	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129473667	TTCAGTGGAGTTTAT[A/G]TGCAGAATTTAAGCT	55764
rs139332053	snp	C/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129471439	TTCAACAGATACTTA[C/T]TGGCACACCTACTGT	55764
rs139375145	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457132	TCCTCGTCTCTCACC[A/G]GAGTAGGTGAAGACC	55764
rs139398399	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475681	TTGCCAGGCATGGTG[A/G]CACTCACCTATGGTC	55764
rs139406308	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444212	CCCTACTTTTTATTC[C/T]GCCATGCTGCTTCTC	55764
rs139511074	snp	G/T	3.29674e-05	0.00405988	missense	IFT122	GRCh38.p7	3:129502800	AGCTGGACAGCCCTG[G/T]CTATGCTGCTGAGAC	55764
rs139515203	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129493963	GAGTGTGCTCTATAT[C/T]GACTGCCTGCAGACT	55764
rs139561230	in-del	-/AGT	0.0123036	0.0774623	intron-variant	IFT122	GRCh38.p7	3:129512094	GTCGGTTTCCTCATC[-/AGT]AGTACTGTGAGGATA	55764
rs139579542	snp	A/C	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129496530	CCAGCTCACAAGTTC[A/C]AGATGGAAAATCTTC	55764
rs139722192	snp	C/T	0.00199136	0.0314915	synonymous-codon	IFT122	GRCh38.p7	3:129488313	GGAAGCCTACCAGAT[C/T]GCTTGCTTGGGTGTC	55764
rs139753511	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129490113	AGCAGTCTTCTTGCC[C/T]CAGCCTCCCAAAGTG	55764
rs139760685	snp	A/C	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129448809	TGATTCTCCTGCCTC[A/C]GCCTCTCGAGTAGCT	55764
rs139790099	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129504054	AAATAAAATGTTTCC[A/G]ATTCTGTGCCGCTTC	55764
rs139901052	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485902	CCTCCGGCCATCCTG[C/T]GGTTTTGGCCCAGAG	55764
rs139910289	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129493583	GTGGAATTCAAGCCC[A/C]GTCTATTTCCTAAGC	55764
rs139940512	snp	A/G	0.000347105	0.0131694	missense	IFT122	GRCh38.p7	3:129519586	GGTGGCTCAGAGTTC[A/G]TGCCAGTGGTGGTGA	55764
rs139940794	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129486237	ACTCACGGGGCAGTC[A/G]GCATGGCAAGCAGTT	55764
rs139943115	snp	A/G	1.64732e-05	0.0028699	missense	IFT122	GRCh38.p7	3:129500025	TCAGCAGGAGAGCAC[A/G]TCAAGGCCATCGAGA	55764
rs139945948	snp	C/T	1.64789e-05	0.0028704	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458643	AAAAGCGTTATTATC[C/T]GGACATCAAAACTGG	55764
rs139950263	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129503115	TCGTTACTGACAGCC[A/G]GCTCTGCCAGGGTGG	55764
rs139962927	snp	C/T	1.64727e-05	0.00286986	IFT122	3	allele_origin=T(somatic)/C(germline)	3:129464725	GGAGAAAGTAAAGAT[C/T]GAGCGGCCGGGGGGC	55764
rs139968880	snp	A/C	0.00716266	0.059414	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438781	AAAAAACAAAAAAAA[A/C]CAAGCAACCGGGCGT	55764
rs139979485	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129443114	TTTATAGGTGTTATC[A/G]TGTTTAATCTCTACA	55764
rs140014915	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129494948	AGTGGATGTTCAGCA[-/TG]CGGGATTTCTTACCT	55764
rs140144353	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449590	TATTATTAGAAGAGT[C/T]AATACCCTCAACAGT	55764
rs140152218	snp	A/G	0.0228947	0.104514	intron-variant	IFT122	GRCh38.p7	3:129450450	GAACCCCTTATGTTT[A/G]ACCAAAAAACCTTTG	55764
rs140152791	snp	G/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129518433	GCTGTAAGCCTGCCT[G/T]CCTTGCAGCTCCCAG	55764
rs140176274	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129451389	CAGCCTCCCAGAGTG[C/T]TGGGATGACAGGAGT	55764
rs140198258	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129465146	GTGTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG	55764
rs140263598	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129518908	GTGTGTGTGGCCTGC[A/G]AGGGGAATGGGTGAG	55764
rs140264485	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129482583	AATTAGAAGGAGTTA[C/T]CTGGCCACCTCTAGC	55764
rs140298823	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129487281	ATTCTCAGGCCTGCA[C/T]GCACATATGCACATA	55764
rs140407982	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129463952	GCTTTCCCTCCCACA[C/T]TTTGATGCTAGACCT	55764
rs140436830	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500869	CCTACAGTCAGACAC[C/T]CCCTCAGGCAGGCAG	55764
rs140469472	snp	A/G	0.0134861	0.0810011	intron-variant	IFT122	GRCh38.p7	3:129468437	CAACTTCCGCCTCCC[A/G]GGTTCTAAGCGATTC	55764
rs140539739	in-del	-/C	0.0726307	0.176182	intron-variant	IFT122	GRCh38.p7	3:129503350	GCCAGTTTTTTCCCT[-/C]CCTTCTCTGCCCCCA	55764
rs140543394	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129506138	TAGACTTTGCCCTGG[A/G]ATTTGGCCCCTCCAG	55764
rs140547512	snp	C/T	0.000181185	0.00951628	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464693	GGGATCATCAGCATA[C/T]GGAACAAAAATGGCG	55764
rs140567547	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129495392	TAACCTTTGTAAAGG[C/T]TGCTTCCTGCCCATG	55764
rs140575442	snp	C/T	8.23608e-05	0.00641667	synonymous-codon	IFT122	GRCh38.p7	3:129512329	AGATCCGTTCAGTGT[C/T]CATCGTCCTGAAACT	55764
rs140619541	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129497529	GATTTTCATACCTCT[C/T]TCCCTGGCTGGCCCC	55764
rs140623081	snp	C/T	0.000315513	0.0125562	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520177	CTGTCTTCCCTTAGA[C/T]GTTCCATTCTGAGGA	55764
rs140623797	snp	A/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129494383	GCAAGATTTCAATTC[A/G]TTTCCAACTATTAGG	55764
rs140756886	snp	A/G	0.29278	0.246313	intron-variant	IFT122	GRCh38.p7	3:129488732	TGTGGGAAGCACCTG[A/G]CTAGTAGCCTGGCAC	55764
rs140805938	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480455	CACGTGTGTTCTTTG[C/T]TCAGCATAAGAAAAG	55764
rs140845292	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459726	TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC	55764
rs140860465	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440925	AAGCTGTAGCTAGCT[A/G]TTGTTGCTAGGGAGC	55764
rs140874687	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511489	TGCTCACAAGAAAGA[A/G]GAGTTACTGGCCTGC	55764
rs140899029	snp	A/G	0.000132207	0.00812934	missense	IFT122	GRCh38.p7	3:129514472	ATGACAAGCTGCGTG[A/G]CCTGTACATCCCTGC	55764
rs140911243	snp	A/G	8.23608e-05	0.00641667	missense, intron-variant	IFT122	GRCh38.p7	3:129492166	GAGTACAAGACCTCC[A/G]ATATTTAGAGCTCAT	55764
rs140927947	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129446114	AAGAAACATTTTACA[A/G]ACTCTCCTCTCTAAA	55764
rs141004492	snp	A/G	0.000153988	0.00877328	synonymous-codon	IFT122	GRCh38.p7	3:129495598	CCTCTGCATGTTTGA[A/G]TATGCCAAGGTAACC	55764
rs141035146	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478969	AGAGAGTGTCTAAGT[C/T]AATGCCAAGAGAAGT	55764
rs141073434	in-del	-/G	0.199873	0.244923	intron-variant	IFT122	GRCh38.p7	3:129447965	TCCATTCAGACGGTT[-/G]GGGGGGGCTTACAAT	55764
rs141111178	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439080	GTGGATGGGTCTAGA[A/G]AGATCATTTAACCCA	55764
rs141142359	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441541	AGCGTCACACAGTGA[A/G]GGGTGGAACCAGCTT	55764
rs141258123	snp	A/G	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129498049	TTCATCACTCAGCAC[A/G]GCCTCTTTCTGTCCA	55764
rs141270433	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129460244	CCCAGCCCCTGAAAA[C/T]CAGCATTCTACTTTC	55764
rs141298928	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129487640	TACCTTTCTTGGACT[C/T]AGTCCCTGGAAGAAG	55764
rs141305406	snp	C/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129467457	AGTAACATTACAAAT[C/G]CTTCGAAGAACATGA	55764
rs141397640	snp	G/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129454593	GAATAATGTTTTAGG[G/T]AGACCTGTGAGGAGG	55764
rs141444464	snp	A/G	0.00080064	0.019992	intron-variant	IFT122	GRCh38.p7	3:129451099	CCATATTACAGCTGG[A/G]TTTTATTTTATTTCT	55764
rs141505236	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129513008	GGAAGATGGCCAAGT[A/G]GATGTTCCAGGGGAG	55764
rs141505375	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475513	AAAAATTAGCCAGGC[A/G]TGTTCTCACACATCT	55764
rs141526316	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129496503	TATTGGTGGGCTACT[A/G]ATGGTAGTTCTCCAG	55764
rs141539693	snp	A/G	0.000115307	0.00759211	missense	IFT122	GRCh38.p7	3:129479864	TCATTCGTTACATCA[A/G]GGTGATCGGTGGCCC	55764
rs141548504	in-del	-/CACA	0.175254	0.238565	intron-variant	IFT122	GRCh38.p7	3:129516220	CGGAGACTGCCTCTG[-/CACA]CACACACAGACTGCC	55764
rs141551785	in-del	-/CTC	0.180702	0.240204	intron-variant	IFT122	GRCh38.p7	3:129509324	GTTCTTCGGCAACTT[-/CTC]CTGTAGTTGTGAGAG	55764
rs141571089	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129479088	AGAAGAATTCCTTAG[A/G]AATCACTGTAGTGTA	55764
rs141589752	in-del	-/AT			intron-variant	IFT122	GRCh38.p7	3:129463279	AACTAAGCCATCACC[-/AT]ATGCAGTTACCACTT	55764
rs141621923	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129483066	TCAGCATTCCCAGCT[A/G]TAACATTGCCTGCTG	55764
rs141626835	snp	C/T	0.000823967	0.0202806	synonymous-codon	IFT122	GRCh38.p7	3:129502768	GCCCCTGCTGCTGTG[C/T]GCTACCTACCTCAAG	55764
rs141632773	snp	A/C	0.000216591	0.0104043	synonymous-codon	IFT122	GRCh38.p7	3:129483652	CTTCTGCCTCCATGT[A/C]TTCTCCATTTCTGCC	55764
rs141732508	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129509201	GACAACACTTCAAAA[C/T]GACTATATTTTCATT	55764
rs141736617	snp	A/G	6.58903e-05	0.00573941	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476426	TCTCTTTTCACCAAG[A/G]ATGGAGTGCGGCTTG	55764
rs141738095	in-del	-/T	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129442242	GAGCATAAGAGTTAA[-/T]TTTTTTAAATCTGTT	55764
rs141739365	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129453015	GAAAGGTTGGAGTTG[-/C]CCCCCCCACTGAGAT	55764
rs141746785	snp	C/G	1.64732e-05	0.0028699	missense	IFT122	GRCh38.p7	3:129500031	GGAGAGCACGTCAAG[C/G]CCATCGAGATCTGTG	55764
rs141807655	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129478480	TCTTGAGACAGACAG[A/G]GTCTTGCTCTGTTGC	55764
rs141810997	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507312	ATGAATACAGTTGGT[A/G]TCTGCCTGCCTTTGT	55764
rs141864185	in-del	-/AC	0.0162398	0.0886349	intron-variant	IFT122	GRCh38.p7	3:129516265	ACACAGACTGCCCCT[-/AC]ACACACACAGATTGC	55764
rs141875475	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129480922	AACAGGCATGGTGGA[A/G]GGTACCTGTTTTCCC	55764
rs141889207	snp	C/G	0.000371364	0.0136215	missense	IFT122	GRCh38.p7	3:129483589	CACCTTCCCTGTGCA[C/G]CGGCAGAAGCTGCAG	55764
rs141936098	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129490016	GATATTTTTATAAAT[A/G]TATATATTTTTATAT	55764
rs141969308	snp	C/T	0.000282235	0.0118759	intron-variant	IFT122	GRCh38.p7	3:129463638	GCAGGTAAGTGCAGC[C/T]CTGACGATAAGATTT	55764
rs141985618	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129454186	TATAATTTTAGTCTG[A/G]TTAGTCCAGTCTCTT	55764
rs142131566	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491082	GAGGGGGACAGGGGC[C/G]GAGACATGTTTCTCC	55764
rs142155283	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480399	GTTAGATGTGGGATA[C/T]CCAGGTTACACAAAA	55764
rs142222993	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491517	ACTGTGAGTTCAAGG[C/T]AAGGGCTGCAATTTT	55764
rs142239831	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129494428	ATGAGCCTGAGCTGT[A/G]TGCAGGTTTTTAGAA	55764
rs142286778	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129450538	AGACTGATTAATCTC[C/T]ATTCTTTGTATGGTT	55764
rs142360341	snp	A/G	0.0236746	0.106192	intron-variant, missense	IFT122	GRCh38.p7	3:129506823	GCTACCTGGGAGCCC[A/G]TAGCTGGACCTGGGT	55764
rs142380592	in-del	-/GGGGG			intron-variant	IFT122	GRCh38.p7	3:129449711	CTGCTGTGGTGTGGC[-/GGGGG]GGTTGAATGGAATTT	55764
rs142458922	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516726	CACACACACACACAC[-/AG]AGAGACTGCCCCTGC	55764
rs142544484	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453173	GGCAAGAGGAGATGG[G/T]ATCTAGGGCATAGAC	55764
rs142546191	in-del	-/ACACAG			intron-variant	IFT122	GRCh38.p7	3:129517298	CACACACACACACAC[-/ACACAG]AGACTGCTCCTGCAC	55764
rs142582724	snp	A/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129501508	TAAAGACAGAGGCAC[A/T]GATTTTGTTCCCCAC	55764
rs142594151	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129505159	TGCCAACAGCTGTGC[A/G]AGGACGAAGAGGCTA	55764
rs142618568	snp	A/G	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129497448	AATGTATAGGAAAGC[A/G]CATTAGAAATGCCAA	55764
rs142635873	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129448145	TCCTCTCCTTGAATT[-/A]AAATGCTGTTGAAGC	55764
rs142641511	snp	C/T	0.000494087	0.0157099	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479814	GTGCCTGTCCTTCAG[C/T]GGAGTGAAGGAGCGG	55764
rs142648422	snp	A/G			synonymous-codon, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520214	GTTGCTGGTGCTTCA[A/G]CATGGCTGCTGCCCC	55764
rs142653024	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473341	TCTAACATTTGGGTC[A/G]TCATGGTTCAGTCTC	55764
rs142654290	in-del	-/C	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129453854	GATTAGTGGGAAGAA[-/C]ATGGGCTTTGGAATG	55764
rs142655964	snp	A/G	0.000379166	0.0137637	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478178	AGAAGTTTGAGTGCA[A/G]CCTCCTGGTGGTGTG	55764
rs142737484	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464129	CTCATGAGTGTAAAG[C/T]GTGCAGGACAGTACC	55764
rs142748345	snp	A/T	0.0333695	0.124785	intron-variant	IFT122	GRCh38.p7	3:129451291	TTTTTATTTTTATTT[A/T]TTTTTATTTTTTGTA	55764
rs142790941	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129486101	AAGTATAGCTCAGAG[A/G]GTATTTGTTCAGTGG	55764
rs142794365	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129517413	ACCCCACCTGCCTGG[C/T]GGCAAGTCCTTTGCA	55764
rs142806153	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129455855	AAATGGAAGTGGATC[A/G]TCATAAAGGTCTTCA	55764
rs142850989	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129480861	TTGGGAGTTAAAGCC[-/A]AATGTTAAAAACAAA	55764
rs142853809	in-del	-/CC	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129472043	CATTTAGTCTGTGGT[-/CC]CCACCCTGCTGAAAC	55764
rs142988936	in-del	-/AGG	0.00159617	0.0282053	intron-variant, cds-indel	IFT122	GRCh38.p7	3:129507264	CCTTATGCTTCTGAT[-/AGG]AGCAGCAGAGGGAAG	55764
rs143033502	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129493044	GCTGGTTTCAAATTC[A/G]TGGGCTCAAGCTATT	55764
rs143075296	snp	C/T	2.2595e-05	0.0033611	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439812	CCCCCAGACTCAGAC[C/T]CTCCAGCCCAGTCGT	55764
rs143085494	in-del	-/CTCAC	0.452103	0.147154	intron-variant	IFT122	GRCh38.p7	3:129504909	AGTGTGAGGCATGGT[-/CTCAC]CTCTACTGAGAATAG	55764
rs143142324	snp	C/T	4.94352e-05	0.00497143	missense	IFT122	GRCh38.p7	3:129483543	ACATGCTCTGCTTCT[C/T]GGGAGGAGGCTACCT	55764
rs143145156	snp	A/G	0.000153988	0.00877328	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469350	TGATTAGAGAGGAAC[A/G]TAATGACATCCTGGC	55764
rs143196031	snp	G/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129469803	TCATTCAACCAGTAT[G/T]TATGAGTACCCACTC	55764
rs143201652	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520498	TAAGGAAAAAAATCT[G/T]TTACTTTCAGAACGG	55764
rs143306012	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129492037	TCCCTTCCTCTCCTC[C/T]GTGGCTCACTGTCTA	55764
rs143334866	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482125	GCGTGGGAAGGAAAC[A/G]GGATGTTTTGTCATC	55764
rs143365183	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500266	CACTAGGGGAAGGGA[C/T]GGTGGGGACCAGGGA	55764
rs143376223	in-del	-/TTTA	0.280789	0.248097	intron-variant	IFT122	GRCh38.p7	3:129470239	ATGGGGGTATGATTT[-/TTTA]TTTATTTATTTATTT	55764
rs143379420	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503757	AAATTTATTAGATTT[A/C]CCAAGCAGCATAGAT	55764
rs143382114	in-del	-/GAGGAG	0.324145	0.238752	intron-variant	IFT122	GRCh38.p7	3:129455899	CAGGTTGAATAGGCT[-/GAGGAG]GAGGAGGAGGAGGAG	55764
rs143445689	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129471139	GAGAAATGCAACCTG[G/T]GCAGTGAAGCCTTTA	55764
rs143470099	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129477528	GATTCTGGCTGTGGT[-/G]GGTTGGGGCAAAGCC	55764
rs143487432	in-del	-/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474995	CCACCTCTAAAAAAA[-/T]ATATTTTTAATTAGC	55764
rs143490747	snp	A/G	0.000703616	0.0187433	missense	IFT122	GRCh38.p7	3:129515578	TGCCGCCAGCCCTTC[A/G]TCTTCTCCGCCTCTT	55764
rs143547321	snp	A/G	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129450911	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCGTGTT	55764
rs143602964	snp	A/G	6.60764e-05	0.00574751	missense	IFT122	GRCh38.p7	3:129519617	GCCGGCTGGTGCTGC[A/G]CTCCATGAGCCGCCG	55764
rs143605827	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129487955	GGCAGAGTGGGGAGG[A/G]GCAAAGGCATTCCAG	55764
rs143645915	in-del	-/ACCTC/TCTCA			intron-variant	IFT122	GRCh38.p7	3:129504908	CAGTGTGAGGCATGG[-/ACCTC/TCTCA]TCTCTACTGAGAATA	55764
rs143659394	snp	A/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129472816	GAGGATTTCTGTTGT[A/T]CAGTATTAAATTTCA	55764
rs143662777	snp	A/C/T	6.58928e-05	0.00573957	missense	IFT122	GRCh38.p7	3:129495564	GGCACGAGAACCTCG[A/C/T]GCTTGAAATGTACAC	55764
rs143670183	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129442661	TCAGCCATTGTCTCC[C/T]GGTCTGCTCCTTTGC	55764
rs143741430	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129511369	AATGCTAAGCTCTGA[A/G]CTGAAGAAGTGTAGA	55764
rs143748879	snp	C/T	0.000197655	0.00993922	synonymous-codon	IFT122	GRCh38.p7	3:129506473	GCTCACAAACAATGC[C/T]GTGGCGGAGAGCAGG	55764
rs143775595	snp	A/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129478836	TTGGTGTACAGAATG[A/T]AGATAGTTTTTATTG	55764
rs143832687	snp	A/G	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129461892	AAATGTCTGTGGAGG[A/G]AGGAAGGGAGTGAAA	55764
rs143880220	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475060	CTGGGGGTGGTGAGG[A/G]GCTGAGGCAGAGGAA	55764
rs143884269	snp	A/G	3.29902e-05	0.00406128	missense	IFT122	GRCh38.p7	3:129502751	GACAAGGCTGAGCGC[A/G]AGCCCCTGCTGCTGT	55764
rs143972725	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498935	TTTGGGTAACTACTC[G/T]GAAAAGAGGTGGTGT	55764
rs143993049	snp	G/T	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129514721	CCCTGTGCTTCCCTG[G/T]CCACCTCCTGTTCTC	55764
rs144031572	snp	C/T	0.000263661	0.0114787	synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461303	TTCCTCCAGTGACTT[C/T]GGTACGTTCTGATTC	55764
rs144094003	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129471539	GGGGTCTTGTTGCTA[C/T]GGCCACAGAAGAAAA	55764
rs144103353	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475728	CTGAGGCAGGAAGAT[C/T]GCTTGAGTCCAGGAG	55764
rs144140226	snp	G/T	0.00143261	0.0267255	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458619	CGCTTTGCTTCTGGA[G/T]CAGCTGACAAAAGCG	55764
rs144202641	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129454212	CTCTTCACTTTAGTC[C/G]TGCATAAAGACATAA	55764
rs144213964	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458100	GTGATGGATATGTTA[A/G]TTAGCTTAATCATTC	55764
rs144240917	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129443415	AGAGAACCATCCTAC[A/G]GTAGAATAGACTGCC	55764
rs144279422	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516842	CAGAGACTGCCCCTG[-/CA]CACACACACACACAG	55764
rs144314242	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129490843	GGCCCATGTGATGCC[C/T]GCATTGCCCTTTTCT	55764
rs144397126	snp	A/C	0.024598	0.108138	missense	IFT122	GRCh38.p7	3:129488348	ACACTGATTGGCGTG[A/C]ACTGGCCATGGAAGC	55764
rs144411048	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490692	ACTCAGACCTCGAAT[A/G]CTCCTTTCCCTCTTG	55764
rs144438445	in-del	-/CA	0.0901694	0.192235	intron-variant	IFT122	GRCh38.p7	3:129516182	CAGAGACCGCCCCTG[-/CA]CACACACACACAGAA	55764
rs144451064	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129502614	CCCATGGGCCATGGC[A/G]TAGTATCAACACTGG	55764
rs144478537	snp	C/T	0.0115144	0.0749975	intron-variant	IFT122	GRCh38.p7	3:129448816	CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGGATTA	55764
rs144515719	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493898	TGAGCTGGGAAGTGC[A/G]TTAAAGTAAACTCCT	55764
rs144605992	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440981	TAAAACTGGAGATGG[A/G]CAGGTATGATCAGAA	55764
rs144611209	snp	C/G/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129511843	GAGGGCTAAATGCCT[C/G/T]TGTTGAAAGACAGGC	55764
rs144615785	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477185	CTCTGGGGTGCTTCT[C/G]CCTCAGCCCTGTCTC	55764
rs144615814	in-del	-/TG	0.126219	0.217206	intron-variant	IFT122	GRCh38.p7	3:129471451	TATTGGCACACCTAC[-/TG]TGTGTACGAGGCACT	55764
rs144627355	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129480696	ATGGGAGCATGGACT[A/G]TGGGGTCAGGTGGGC	55764
rs144640118	snp	A/G/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129446198	TTTATCTTAACCCAG[A/G/T]CATTCCTTTCTGTTG	55764
rs144656358	in-del	-/ATATTT			intron-variant	IFT122	GRCh38.p7	3:129454509	TGTACCATGGTAGTC[-/ATATTT]GTGTGTGTGTGTGTG	55764
rs144663082	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129517928	ATGATGTCATGATGT[C/T]GGTGTTGGCCCCCAG	55764
rs144727222	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469384	GGCTGACTGGGGACA[A/G]AAAGTTTCCTTCTAC	55764
rs144831946	snp	A/C	6.58913e-05	0.00573945	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504370	GATGACATCTACATG[A/C]CGTATGCTCAGTGGC	55764
rs144875186	snp	C/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129519438	GAGGAGCTTGCCACT[C/G]TTAGGGTCACCTGGG	55764
rs144877247	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129450533	TACGCAGACTGATTA[A/G]TCTCCATTCTTTGTA	55764
rs144961252	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510116	CCCAAGGTGGAGTGC[A/C]GTGTCATGATCATAG	55764
rs144972161	snp	A/G	3.32912e-05	0.00407976	missense	IFT122	GRCh38.p7	3:129495450	AATTTTTCCAGGAGA[A/G]GAAGAAGCGGGGAGA	55764
rs145009974	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129460499	TCCTGAGCTCAAGCA[A/G]TCCTTCTCCCTTGGC	55764
rs145016465	snp	A/G	0.0142736	0.0832652	intron-variant	IFT122	GRCh38.p7	3:129491351	GCAATAAATGGTGAC[A/G]GCAAAGCCACCTGAA	55764
rs145072076	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468051	CACTGGTGGGCTGGG[A/C]TCCTGGATTGTGTTT	55764
rs145141171	snp	C/G/T	0.0489162	0.149731	intron-variant	IFT122	GRCh38.p7	3:129465539	GCAGTGGCACAATCT[C/G/T]GGCTCACTGCAACCT	55764
rs145212370	snp	A/G	3.29451e-05	0.00405851	missense	IFT122	GRCh38.p7	3:129506427	TCCACAAGGCTGGGC[A/G]ACAGAGAGAAGCGGT	55764
rs145239724	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476868	AAGGGCTGGTGACAG[C/G]GCACTTGAAATGACA	55764
rs145270542	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482675	GGGGAAAGAGAGGGC[A/G]TAGCCTTCAAGCTGA	55764
rs145346042	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504637	CACTCACTTGCCACA[A/G]GCCCTTAAGAGGTGC	55764
rs145353293	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509890	TCAGCTTCTTTCTCT[A/G]TAAAATAGGGATAAC	55764
rs145356237	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438971	AACTTCATTAAAGTT[C/T]CAATGTGTCTTCTAT	55764
rs145394431	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129481908	GACCGGCCTCTTTAA[A/C]TTTGGTTTCCTTGCC	55764
rs145418301	snp	A/C	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129443249	TCAGATGATGCAGGA[A/C]TTGGAGAGGCACTGT	55764
rs145441726	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129489008	CCTCTCTGCACATAA[A/G]GAAAAGCCCAGGTAT	55764
rs145454020	in-del	-/GGGGGGGGG			intron-variant	IFT122	GRCh38.p7	3:129454650	CTCATCCTAGTGGCT[-/GGGGGGGGG]GTTGAGGAATGTGGG	55764
rs145470016	snp	C/T	0.00034587	0.0131459	missense	IFT122	GRCh38.p7	3:129512333	CCGTTCAGTGTCCAT[C/T]GTCCTGAAACTCTTT	55764
rs145501141	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129446405	AATTTTTTGTAGAGA[C/T]GGGGTTTCACCGTGT	55764
rs145668609	snp	A/G	0.0134861	0.0810011	intron-variant	IFT122	GRCh38.p7	3:129497358	GGGGAAAGGCTCTTC[A/G]GTTTGCCAAACCTCC	55764
rs145715893	in-del	-/T	0.213333	0.247296	intron-variant	IFT122	GRCh38.p7	3:129456501	ATTAGCTGGGCATGG[-/T]TGGTGTGTGCCTGTA	55764
rs145719710	snp	A/C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129497647	ACACTCCATTTGCTC[A/C/T]GTCTCTCTATGAAGG	55764
rs145749386	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504152	TGTTTTCGAAGAGCT[A/G]ATTTGTTTTTGCATT	55764
rs145781271	snp	G/T	0.000399281	0.0141238			GRCh38.p7	3:129471828	TTTGTCATTTGAAGT[G/T]TTAGTAATACTTAAG	55764
rs145790923	snp	G/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440598	CTGAGGTGGTGGCGG[G/T]TGGAGGCGGCTCTTC	55764
rs145855324	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510435	GACCTCATCTTCCCT[G/T]ACAGTCTTTGGCTTT	55764
rs145911209	snp	A/C	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129489564	AGAGGAGGGGCCAGG[A/C]GCGGTGGCTCACGCC	55764
rs145979250	in-del	-/AAG	0.0551013	0.156571	intron-variant	IFT122	GRCh38.p7	3:129443708	ATCTAACACAATGTA[-/AAG]AAGACTGTATAAGTC	55764
rs145997332	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491564	GTTTGCCTTCCACAG[A/T]CTTGGTGGGATTCAT	55764
rs146026277	snp	A/C	0.00125119	0.0249806	missense	IFT122	GRCh38.p7	3:129499987	ATATCAAGGAGCCCA[A/C]AGCCGCCGTGGAGAT	55764
rs146041987	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129503087	TTGTCCCTTCATTCA[A/G]TCATTGAGAAAATCG	55764
rs146047989	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129456323	ATATGGCTCACCCTA[A/G]TATCTACTATTTCAG	55764
rs146167147	snp	C/T	0.0119091	0.0762411	intron-variant	IFT122	GRCh38.p7	3:129451369	TTCAAGCAATCCTCC[C/T]ACTTCAGCCTCCCAG	55764
rs146190693	snp	A/G	0.000767705	0.0195771	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476800	GATCACTGAGCAGAA[A/G]GGTAAGAGGCAGGTC	55764
rs146233778	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503907	TGGGTCCATACAGCA[C/T]GAAGCCCACAGTCAT	55764
rs146257299	in-del	-/TTTTA	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129478433	GAGAATGTTTTTTTG[-/TTTTA]TTTTATTTTATTATT	55764
rs146267058	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129507866	ATGTAACCCACTGGT[C/T]ACAGTGAACTGCTGA	55764
rs146270512	snp	A/G	6.7981e-05	0.00582974	missense	IFT122	GRCh38.p7	3:129483591	CCTTCCCTGTGCACC[A/G]GCAGAAGCTGCAGGG	55764
rs146397021	snp	C/G/T	4.94184e-05	0.00497063	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466971	TATTCAGGAAATCCC[C/G/T]TCCACTCTGAAGTCA	55764
rs146407985	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490069	GGACTCACTGTGTTG[C/T]CCAGGCAGGTCTTGA	55764
rs146466111	snp	C/T	0.0287284	0.116357	intron-variant	IFT122	GRCh38.p7	3:129488669	CTGTAAAGCCTGACC[C/T]AGGAGCAGCATGTCA	55764
rs146478706	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497469	GAAATGCCAACCTGT[A/C]GAAAGATTAGGAAGA	55764
rs146530833	in-del	-/T/TT	0.12932	0.218944	intron-variant	IFT122	GRCh38.p7	3:129460447	TTTTTTTCTTTATTA[-/T/TT]TTATTTTTTTTTATG	55764
rs146575573	snp	A/G	0.0236746	0.106192	intron-variant	IFT122	GRCh38.p7	3:129497741	TTTTCAATCCCCCCT[A/G]CCCCCACCTGGTAGT	55764
rs146579996	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129500391	ATGCCATCAGGGCTG[G/T]TGTCTCCTCGCCCAC	55764
rs146593426	snp	A/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129445830	GCATTTTAAGAGCTC[A/C]GCAGGTGCTGTCTGG	55764
rs146611342	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449454	AGTAATTTCCCTGAG[G/T]GGAGGGAGGGATTAT	55764
rs146653997	snp	A/G	0.000153988	0.00877328	missense, intron-variant	IFT122	GRCh38.p7	3:129460984	TGCTTGAGGCCAAGC[A/G]TTCAAAACCAACCTG	55764
rs146697109	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129482324	GCAGCTCTGTGCCCC[A/G]GGCCTGGTTGGCTTT	55764
rs146717067	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129467370	CTCCTCAGTCTTTTC[A/G]TGTGTTCATATAATT	55764
rs146751064	snp	C/G/T	0.0107246	0.0724382	intron-variant	IFT122	GRCh38.p7	3:129471279	CATTTCTTTTGTATT[C/G/T]GAGTAAAGAAAAGAT	55764
rs146778076	snp	G/T	0.000263996	0.011486	synonymous-codon	IFT122	GRCh38.p7	3:129519666	ATGGCCCCCACCCCT[G/T]AGGTGGCAATACTTC	55764
rs146817243	snp	A/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129505682	CAAGTGCTTCACTGG[A/C]AGCCACCAACATCTC	55764
rs146818318	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129469480	TCATTTTCTGAGATT[C/G]TGTTACTATTAATTA	55764
rs146818399	snp	G/T	0.000444668	0.0149042	missense	IFT122	GRCh38.p7	3:129506507	AATGATGCTGCCTAT[G/T]ATTACTGGATGCTGT	55764
rs146839438	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486354	TGGGGCCTCATTTCT[C/T]TTCTGTGAAATGGGG	55764
rs146874343	snp	C/T	0.0063408	0.0559481	synonymous-codon	IFT122	GRCh38.p7	3:129488259	TGAAATCCTGCAGTC[C/T]GCTCCCATGTACCAG	55764
rs146913890	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129473499	TATGTTTGTGTGTAT[A/G]TATGTTTAAGCAGGC	55764
rs146987467	snp	C/G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487682	GACCGCTTCCTCCCA[C/G/T]GAACTCATTCATTGT	55764
rs147017409	snp	C/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129489321	CAGGCCAGCCACTTT[C/G]CTTGGAGCCCCAGTC	55764
rs147162880	snp	A/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129496874	TCTCTGCTTCCGGGG[A/T]TAACAAAATTTTAAC	55764
rs147179235	snp	C/T	0.0614824	0.164198	intron-variant	IFT122	GRCh38.p7	3:129498970	AGGCTGTTTCTCACA[C/T]ATTGTAGGGCCAGCC	55764
rs147179501	snp	A/G	0.126219	0.217206	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457797	CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT	55764
rs147181689	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129442777	CTAGAGTGATTCCCA[A/G]TTACTTTCCATGTCA	55764
rs147268604	snp	A/G	0.0256215	0.110247	intron-variant	IFT122	GRCh38.p7	3:129515863	AACCAAATGCCCCAG[A/G]AAGAGAGTCCGATGG	55764
rs147285273	snp	C/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129517680	AGGGCCCAGTCCCAG[C/G]GGATCGCGGGCCATG	55764
rs147288978	snp	A/G	0.000599022	0.017296	intron-variant	IFT122	GRCh38.p7	3:129463644	AAGTGCAGCTCTGAC[A/G]ATAAGATTTATGTTC	55764
rs147341636	snp	C/T	0.000363973	0.0134853	missense	IFT122	GRCh38.p7	3:129514532	CCCTGACCATCCGCG[C/T]CAAGCCCTTCCACGA	55764
rs147356926	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464232	AGCATCTGTTGAGCA[C/T]CTTCTACAAAGCAAG	55764
rs147385966	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129469951	GTGGTATGTGACACA[A/G]TAGAAAGCTGTACAG	55764
rs147394250	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129485185	CCTGTCCCAACTTGG[C/T]GCCTTGGCATAAATT	55764
rs147411001	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516308	CACACACACACACAC[-/AG]AGACTGCCCCTGCAC	55764
rs147495444	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129487966	GAGGGGCAAAGGCAT[G/T]CCAGGTGAGGGTGAC	55764
rs147499719	snp	C/T	6.58913e-05	0.00573945	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504371	ATGACATCTACATGC[C/T]GTATGCTCAGTGGCT	55764
rs147517019	snp	A/G	0.000148416	0.00861312	missense	IFT122	GRCh38.p7	3:129517471	CTATGCCCTCCAGAC[A/G]TGCTACACCTGGTTG	55764
rs147554530	snp	C/T	0.0267878	0.112589	intron-variant	IFT122	GRCh38.p7	3:129494126	CTGAGTGCCATAGAT[C/T]GTTTTTATTGGTCAT	55764
rs147583970	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129453781	AAGGAAGGGAAGTGG[C/T]GCATGAAACTGAGAT	55764
rs147643126	snp	A/G	0.0360663	0.129354	intron-variant	IFT122	GRCh38.p7	3:129491480	AACTTCTAGAGGTCC[A/G]TGAGTTAAAGTCTCT	55764
rs147655908	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438974	TTCATTAAAGTTCCA[A/G]TGTGTCTTCTATGAT	55764
rs147660181	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509973	AAGAGTACCTAGCAC[A/G]GAGTGACCCTAGGTG	55764
rs147682642	in-del	-/GAG	0.187053	0.241946	intron-variant	IFT122	GRCh38.p7	3:129455899	CAGGTTGAATAGGCT[-/GAG]GAGGAGGAGGAGGAG	55764
rs147759645	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458251	AGGATCCGTGTCTTA[C/T]CATGTTGTATTTGTG	55764
rs147810031	in-del	-/AT	0.0271762	0.113356	intron-variant	IFT122	GRCh38.p7	3:129504824	TTTGCCTGAAGTTTC[-/AT]AGCTAGGAAGTGGCA	55764
rs147861735	snp	C/G	0.00716266	0.059414	intron-variant	IFT122	GRCh38.p7	3:129454498	GTCAGGTGTGCTGTA[C/G]CATGGTAGTCATATT	55764
rs147869084	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129480712	TGGGGTCAGGTGGGC[C/T]GGAGGTCGTGTTCTT	55764
rs147887396	snp	A/G	0.000115309	0.00759218	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479817	CCTGTCCTTCAGCGG[A/G]GTGAAGGAGCGGGAG	55764
rs147967866	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129477620	GTGTAGAGCCTGGTG[C/T]GTACCAGAAATTACA	55764
rs147990725	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129502653	GAATGAATGGACATA[C/T]GGCTTGCCGTTGACA	55764
rs148026867	snp	A/G	3.3066e-05	0.00406595	missense	IFT122	GRCh38.p7	3:129514438	GCCCTCGGTGCCTAC[A/G]GGCTGGCCCGGCACG	55764
rs148061854	snp	C/G	0.111224	0.207945	intron-variant	IFT122	GRCh38.p7	3:129517085	CTGCACACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs148130660	snp	A/G	0.0150606	0.0854603	intron-variant	IFT122	GRCh38.p7	3:129478913	GAAGTTTTAATTCCT[A/G]AAAGATTTTTTTTCA	55764
rs148165380	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129461915	GAGTGAAATTGGGCA[A/G]AGGCTTGTAGGTTAT	55764
rs148188237	snp	C/G	0.000181358	0.00952083	synonymous-codon	IFT122	GRCh38.p7	3:129502759	TGAGCGCGAGCCCCT[C/G]CTGCTGTGCGCTACC	55764
rs148202272	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475487	AGAAACACCGTCTCT[A/G]CAAAAAATACAAAAA	55764
rs148327899	snp	C/T	0.0271762	0.113356	intron-variant	IFT122	GRCh38.p7	3:129450921	GAGACGGGGTTTCTC[C/T]GTGTTAGCCAGGATG	55764
rs148342188	snp	A/G	0.00993419	0.0697739	intron-variant	IFT122	GRCh38.p7	3:129505754	AAACAGTATAGGAAC[A/G]ATTGAGAGTTTTTTT	55764
rs148434524	snp	G/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129452871	TGGCTCAGACCTCTG[G/T]GGGGGCAGAGGAGGT	55764
rs148462309	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129508181	CACTTTCCCTCTCTG[C/T]CCCTCAGTTTCCTTC	55764
rs148471238	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497419	TCAGTTTAGTCATGA[G/T]ATTTGCACAGAATAA	55764
rs148540595	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129515274	CAGGTGTCTTGGGCA[C/T]GGGGACCCAAGTGAC	55764
rs148626512	snp	A/G	0.000263713	0.0114799	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478120	GAGTTGTATTCAGAG[A/G]ACTTATCAGACATGC	55764
rs148673973	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129480372	TCATAAGCAAAATGG[G/T]CCCTTTGGCCAGTTA	55764
rs148873036	snp	A/C/G	0.00398731	0.0445001	intron-variant	IFT122	GRCh38.p7	3:129491942	TTTGCTGTTCTTTAC[A/C/G]TGGTCCAATCCCATG	55764
rs148941657	snp	A/G	0.000214272	0.0103484	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504441	GCAACACAGACTGTC[A/G]CCTTCTAGAAGGAGC	55764
rs148945116	snp	C/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129472108	GTCTATCAGATTAGT[C/G]TTGCAATGACCATTC	55764
rs148959438	snp	A/T	0.0166325	0.0896639	intron-variant	IFT122	GRCh38.p7	3:129455247	GCGCGATCTCGGCTC[A/T]TGGCAACCTCTGACT	55764
rs148987764	snp	A/C	0.0107246	0.0724382	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440121	TAGGGGCTCCAGTGC[A/C]ACCATTGCTTTTGCT	55764
rs149029829	snp	A/G	0.00122104	0.0246785	missense	IFT122	GRCh38.p7	3:129519629	TGCGCTCCATGAGCC[A/G]CCGGGATGTCCTCAT	55764
rs149045369	snp	G/T	0.0166325	0.0896639	intron-variant	IFT122	GRCh38.p7	3:129487460	GCACAGGACTGTGGG[G/T]ACAGCCAAAAGCCTT	55764
rs149143054	in-del	-/TTT			upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440244	GGTAGCCAAAGTGGC[-/TTT]TTGTGGAGTGGCGAC	55764
rs149152354	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129500400	GGGCTGGTGTCTCCT[C/T]GCCCACCTTGCAGAT	55764
rs149203656	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482065	CCTTTGCAGAAGTCT[A/G]TGTCTCACCTGCTGC	55764
rs149245630	snp	A/G/T	4.96326e-05	0.00498139	missense	IFT122	GRCh38.p7	3:129514531	ACCCTGACCATCCGC[A/G/T]CCAAGCCCTTCCACG	55764
rs149264103	snp	C/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129502464	TTGTTTCTATACCCT[C/G]CTGGATAGCTCAGTG	55764
rs149308467	snp	A/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129484927	TGTTGGCATGTGTAA[A/T]CTCCCACCACAGTCA	55764
rs149345836	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129461509	TTACTCTGGTAAGAC[A/G]TCAGAGACTACAGGA	55764
rs149351049	snp	C/T	0.0107246	0.0724382	intron-variant	IFT122	GRCh38.p7	3:129517917	CAACATGGGACATGA[C/T]GTCATGATGTCGGTG	55764
rs149361976	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129447837	CATACTTAAAGTCTG[C/T]GTTGATATTAATGCC	55764
rs149422533	snp	A/G	0.0185938	0.0946107	intron-variant	IFT122	GRCh38.p7	3:129498608	ATCATATATTAGGCC[A/G]ACCTAATACTCTGAA	55764
rs149465667	in-del	-/G	0.0205511	0.0992634	intron-variant	IFT122	GRCh38.p7	3:129464377	AAGGGCTGTCATAGA[-/G]GGTATGTACAGAGGG	55764
rs149476572	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474795	AGAAAAGACAACCCA[C/T]AGAATGAGAGAAGTT	55764
rs149513210	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129513986	GGTTGAGGGTGGCTC[C/T]CCAGGGAGTCTGGAC	55764
rs149578956	snp	C/T	0.000844296	0.0205289	missense	IFT122	GRCh38.p7	3:129481617	GACATGAGTGCCTCC[C/T]GTAAGAAGCTGGCCG	55764
rs149611043	in-del	-/A			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438772	AAAACCCAAAAAAAC[-/A]AAAAAAAAACAAGCA	55764
rs149628833	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469210	AAATTATAACTTTTG[A/G]CTTCAGTAAAGCTGT	55764
rs149807071	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129504062	TGTTTCCGATTCTGT[A/G]CCGCTTCTGTGGTCC	55764
rs149813360	in-del	-/ATG	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129446094	ACACAGACTTTAAGT[-/ATG]ATAAGAAACATTTTA	55764
rs149824116	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129493616	ATGCTCTCTCGGCCA[C/T]ATACCCTCCCTACCC	55764
rs149825238	snp	A/G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486270	TGTGGTTCGGGGAAG[A/G/T]AGCACCAGCTTTCAG	55764
rs149872501	snp	C/T	0.0287284	0.116357	intron-variant	IFT122	GRCh38.p7	3:129465060	AAAGTGTGTGTGTGG[C/T]GTGTGTGTCTGCGCA	55764
rs149884307	snp	C/T	0.00258349	0.0358479	synonymous-codon	IFT122	GRCh38.p7	3:129519147	GACCAAGGACTCCAT[C/T]GGAGATGAGGACCCG	55764
rs149915993	snp	A/C	0.000165027	0.00908221	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478075	AGAAATCGATTGGCT[A/C]TCCAACTGCCAGAGA	55764
rs149929955	in-del	-/AG	0.093777	0.195178	intron-variant	IFT122	GRCh38.p7	3:129452844	AAGCATCATCCAGAC[-/AG]GGGGTGATGGTGGCT	55764
rs150001203	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476770	TAGCATGACTGACGT[C/T]ATTGTGCAGCACCTG	55764
rs150029312	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457235	AAATTACTTGTTATA[G/T]GTTGCCTCTCTCCAG	55764
rs150041434	snp	C/G	0.266	0.249487	intron-variant	IFT122	GRCh38.p7	3:129516605	CCCTGCACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs150055466	snp	C/T	0.000477677	0.015447	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504414	TCGCTTTGAGGAAGC[C/T]CAGAAAGGTAGGCAA	55764
rs150070264	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129480998	GTTTGAGGCTGCAGT[A/G]TGATATGATTATACC	55764
rs150121048	snp	A/T	0.021333	0.101051	intron-variant	IFT122	GRCh38.p7	3:129479009	CTTTGAGAGAAGGCT[A/T]GCCCAGCATCTTGGA	55764
rs150137967	snp	A/G	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129460080	TAAAATATACATGAC[A/G]TAAAATTTATCATAT	55764
rs150163240	snp	A/C	3.30513e-05	0.00406504	synonymous-codon	IFT122	GRCh38.p7	3:129514503	CAGATTCCAAAAGTC[A/C]ATTGAGCTGGGTACC	55764

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