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
rs150174636	snp	G/T	0.0231265	0.105019	synonymous-codon	IFT122	GRCh38.p7	3:129483544	CATGCTCTGCTTCTC[G/T]GGAGGAGGCTACCTC	55764
rs150297599	snp	A/C	0.00597247	0.0543191	intron-variant	IFT122	GRCh38.p7	3:129450499	CTAAGTCTACTTCCT[A/C]TTCTCTGTTGTCTCT	55764
rs150331350	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129506293	GCACTGCAGATGCTC[C/T]AATGAGTGTCCTACT	55764
rs150351247	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455212	AAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	55764
rs150388125	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513079	GGTGAGGGGACCCTG[A/G]GTGGGAGGGGCCGGA	55764
rs150390285	snp	C/T	4.94214e-05	0.00497074	synonymous-codon	IFT122	GRCh38.p7	3:129479871	TTACATCAAGGTGAT[C/T]GGTGGCCCTCCTGGA	55764
rs150396788	in-del	-/AGGCG	0.499722	0.0117779	intron-variant	IFT122	GRCh38.p7	3:129513886	GGGGCCCCAGAGCAC[-/AGGCG]AGGCTGCCGCTCAGA	55764
rs150400932	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468554	TCCCCATGTTGGCCA[G/T]GCTGGTCTAGAACTC	55764
rs150496357	snp	A/G	0.000592846	0.0172067	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464749	GGGGGGCTCCCTCTC[A/G]CCAATATGGTCCATC	55764
rs150497198	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129470758	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	55764
rs150498947	snp	A/G	3.64425e-05	0.00426848	synonymous-codon	IFT122	GRCh38.p7	3:129483673	CATTTCTGCCGTGGA[A/G]GTGCCGCAGGTAACT	55764
rs150550701	snp	A/G	0.00640566	0.0562299	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476757	ATGCCTACAGGGATA[A/G]CATGACTGACGTCAT	55764
rs150619632	snp	A/G	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129489754	TGAGGCAGGAGAATG[A/G]CGTGAACCTGGGAGG	55764
rs150649189	snp	A/G	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129447747	CAAACTCCTGACCTC[A/G]TGATCCGCCCGCCTC	55764
rs150653708	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129480423	CACAAAATTCTGTGT[A/G]TGTGTATACATGTGT	55764
rs150686552	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129518295	CAGGAGGATGCACCA[A/G]GGCAGTTGTCCAGGG	55764
rs150688520	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129493400	AGCCTGCTAAGCCTC[A/G]TAACGTAATCTGCTC	55764
rs150690971	in-del	-/A	0.127254	0.217792	intron-variant	IFT122	GRCh38.p7	3:129445325	GCAAGACTCCACCTC[-/A]AAAAAAAACAAAAAC	55764
rs150692598	snp	A/G	0.00102121	0.0225735	synonymous-codon	IFT122	GRCh38.p7	3:129519177	GTTCACAGCTAAGCT[A/G]AGCTTTGAGGTGAGG	55764
rs150706577	snp	A/G	0.0271762	0.113356	intron-variant	IFT122	GRCh38.p7	3:129499313	TTCAGGGCACAGAAT[A/G]TTTGCTGGTGACTCA	55764
rs150778761	snp	C/T	6.69366e-05	0.00578479	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439824	GACTCTCCAGCCCAG[C/T]CGTGCCCATCGAGCA	55764
rs150830787	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129451237	CCGAGTAGCTAGGAC[C/T]GTGGACACACACCAC	55764
rs150862636	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129509479	TGTTAGCAGTTCCTG[G/T]GCCAAATGCGTTGTC	55764
rs150881592	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456871	CGGTGAGCCGAGATC[A/G]TGCCACTGCACTATA	55764
rs150958123	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129511419	GTTCAGACCAATTAG[A/G]GGTTAAGCTTTGGTG	55764
rs151006097	snp	A/G	0.0622301	0.165053	intron-variant	IFT122	GRCh38.p7	3:129459435	GCTGGGACTATAGGC[A/G]CTCACCACCATGCCA	55764
rs151080965	snp	A/T	1.64808e-05	0.00287057	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478156	CGGGTAAAGGAGAAG[A/T]TTATCAAGAAGTTTG	55764
rs151126891	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486228	GCCTGTCCCACTCAC[A/G]GGGCAGTCAGCATGG	55764
rs151163335	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129491152	GGATGAAAAGATAAA[A/G]TTGCATTGTGGTCAC	55764
rs151216801	snp	A/C	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129494759	TGTGTGATACAAGGA[A/C]TATCTGGAGTCAGAC	55764
rs151238429	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500809	CACTGGAAGGGCCTC[C/T]GATGCCAAACGGAGG	55764
rs151267851	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468132	CATTAACATCCCTCT[C/T]GGTCTTTGTCTCTTT	55764
rs151309730	snp	A/G	4.94173e-05	0.00497053	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464676	CGCTGGGGATGTTCA[A/G]TGGGATCATCAGCAT	55764
rs151338787	snp	C/G	0.0146672	0.084371	intron-variant	IFT122	GRCh38.p7	3:129444198	TGGCCCCACGTCCCC[C/G]CTACTTTTTATTCCG	55764
rs181000265	snp	A/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474540	TGGGAGGATGAGGGG[A/T]TGGGGATTGGAGATG	55764
rs181000640	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129458938	GACATTGTAGACTTT[A/G]TCCCACCCCCAACCT	55764
rs181012261	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129451223	CCCACCTCAGCCTCC[C/T]GAGTAGCTAGGACTG	55764
rs181014683	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129518679	ACCAGCCCCACCACT[A/G]TGGGAGAGGGGCGGT	55764
rs181042858	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490600	AGAAAGACCCTTGAG[A/C]GGGTGTCAGTAGCAG	55764
rs181043647	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129467714	CATGGGCAGGCCAGA[A/G]TGGGGAAAGCTGGGG	55764
rs181071642	snp	C/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129510830	CGTGACAGACCCTGT[C/G]ATGAGACCTGGTGAC	55764
rs181142420	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129462251	AAAAAGGCAAAATAG[A/T]ATCCCTACCCTCAAG	55764
rs181149362	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482511	TACCAGGCTCCTCCT[C/T]GTTCTCAGCAGCAGA	55764
rs181161475	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129442796	CTTTCCATGTCAAGT[C/T]GTGCATTTTGCTAGA	55764
rs181164193	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129495226	AACAAACAAAGGTTT[A/G]CATCTTTTTTTGATC	55764
rs181168926	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455659	TGCAATAAAAAATCT[G/T]CATGTAATTTCTGAA	55764
rs181171202	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129470364	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTACCT	55764
rs181174242	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515130	CCCACAGGTAGTTGT[A/G]AGGCTAAATGAGCCA	55764
rs181205401	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487387	TGCTGGGACAGGTCA[G/T]TTGTCCTCTCTGAGT	55764
rs181218428	snp	C/G/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129509488	TTCCTGGGCCAAATG[C/G/T]GTTGTCGATGTTACG	55764
rs181290625	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475316	GCATTCACTTGAAAA[G/T]TGTAGCAGTTCCTAA	55764
rs181318594	snp	C/T	0.000297339	0.0121894	missense	IFT122	GRCh38.p7	3:129519616	AGCCGGCTGGTGCTG[C/T]GCTCCATGAGCCGCC	55764
rs181371338	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459521	GTCTCGATCTCCTGA[A/C]TACATCTATTTTTTT	55764
rs181401321	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499465	TAAGATGACAGGTCT[C/T]GATATGTGGAATTGT	55764
rs181542062	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129449712	CTGCTGTGGTGTGGC[A/G]GTTGAATGGAATTTG	55764
rs181547120	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129466684	TTTTTTGTATTTTTG[A/G]TAGAGACAGGGTTTC	55764
rs181646804	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129462821	GGGCATCTGGGACAG[A/G]GGGGAGCAAGCCTTA	55764
rs181654657	snp	C/G	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129513999	TCCCCAGGGAGTCTG[C/G]ACCAGGCCCCACCTG	55764
rs181659096	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129444354	CCCAGCTGGAAAGAG[G/T]GTGATAATCATCCTT	55764
rs181660491	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129494002	CACATCTGGGTGCTC[A/G]GCATAATTCCAGAGA	55764
rs181665283	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482798	AGTAATTGCCCCTTA[C/T]AGAATTGCTACAGGA	55764
rs181783000	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489925	CCACCCAGAAATGCC[A/G]GCAGGGAGGGAGACG	55764
rs181789156	snp	C/T	4.94189e-05	0.00497062	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466932	AGAGAATGAGGATGC[C/T]GAGGATGTCATTGTC	55764
rs181795242	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510410	CACAGCAGGGTCAGT[C/G]GTCTCAAGGGACCTC	55764
rs181838911	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454556	GTGTGTGTGTGTGTG[C/T]GCATGTTTGAGTTCA	55764
rs181908469	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505405	GCCCCTCAACCGAAA[A/G]CCCTCATTGAAGGTT	55764
rs181971625	snp	A/C/T	4.94412e-05	0.00497178	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458604	ACACTTTTAGGCAAG[A/C/T]GCTTTGCTTCTGGAT	55764
rs182114566	snp	C/G	0.00953873	0.0683987	intron-variant	IFT122	GRCh38.p7	3:129468835	AGTCAGAAACCATTT[C/G]ACCTGTGCAAGGACC	55764
rs182126079	snp	C/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129469799	TCTTTCATTCAACCA[C/G]TATTTATGAGTACCC	55764
rs182157328	snp	C/T	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129514907	TACTCTAGAAACCTC[C/T]GCCCTTTCTGGAACC	55764
rs182163706	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504966	ATAAACGGGTGACTT[A/C]TGCTCCTCAAGAATT	55764
rs182347099	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129478285	CCCCAGTGATAGGGT[A/G]CCCACCTCATGGTTT	55764
rs182360171	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501614	TTTCTTGTCACTTTC[A/G]TTTGTAAGTGCTATA	55764
rs182409857	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129455331	GCACGCGCCACCATG[C/T]CTAGCTAATTTTTGT	55764
rs182412246	snp	G/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129494725	TGTTGGGGACATCAC[G/T]TGCTTCAAAAGACTA	55764
rs182482045	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497603	CTTCGTGTGCCCACA[A/G]CCTCCCACCAGAACT	55764
rs182714728	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129451671	GAGTGAGTAATTGAA[C/T]CTTTGGTTCTCAAGG	55764
rs182714874	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491816	CCCCAGAGGGTCAGA[A/C]CGGCTTGTTCTTCTT	55764
rs182720847	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468107	CACAAAGGTCATCTG[C/G]AGGCTCCCTCATTAA	55764
rs182727122	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511323	TGGAGCTAACAAAAG[G/T]TATAGAAATTTACGT	55764
rs182864051	snp	A/G	0.00318978	0.0398085	intron-variant, missense	IFT122	GRCh38.p7	3:129506730	CAGTTTGCCCATCAG[A/G]ATGGTATGAGGACCG	55764
rs182897945	snp	C/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129506215	CAAAAAGGAATTTAT[C/G]TCACTGTACTTTTTC	55764
rs182903744	snp	C/T	0.0123036	0.0774623	intron-variant	IFT122	GRCh38.p7	3:129463924	TGTCCAGGCAGCATG[C/T]GTGGGGAAGAAAGCT	55764
rs183040424	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441279	CTGAGATCTTTCTCT[A/G]TGTAAAGCATGCCGT	55764
rs183055588	snp	C/T	0.0154073	0.0864077	intron-variant	IFT122	GRCh38.p7	3:129479971	TAATCTGCATGCACA[C/T]GTGGGTGACCCGTCT	55764
rs183136889	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459674	TCCTTCCTTCCCTCC[C/T]TCCCTCCCTTCTTCC	55764
rs183154091	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439137	GCAAGAACTAGAATT[A/G]GAATCAAGGTTTTCT	55764
rs183158342	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129446089	CATCAACACAGACTT[A/T]AAGTATGATAAGAAA	55764
rs183161327	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477738	CTAGTGCTGTGCAGA[A/G]GAGTTTATATTTGTA	55764
rs183190773	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129485186	CTGTCCCAACTTGGC[A/G]CCTTGGCATAAATTC	55764
rs183197104	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129447059	GCCTCATTTCTCCAT[A/G]TTCTAGCAACATCTT	55764
rs183200444	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129486227	TGCCTGTCCCACTCA[C/T]GGGGCAGTCAGCATG	55764
rs183204439	snp	A/G	0.00597247	0.0543191	intron-variant	IFT122	GRCh38.p7	3:129515681	CTCTGGCCTCAGGAC[A/G]TTGGGCAAGGGCCAA	55764
rs183268146	snp	C/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129483306	TGGAGGGGCTTGCCT[C/G]TGTTCATTTCTCTTG	55764
rs183269216	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456796	TGGTGGGCACCTGTA[G/T]TCCCAGCTACTCGGG	55764
rs183275996	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129462938	AAAGCATCATTGTTA[C/T]TTTAAATGCTAGGTT	55764
rs183309494	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512167	ACAGTGGCTATATGG[C/T]GCTCAGCACACAGTA	55764
rs183335606	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129460790	TAAAACGGGTTGAGA[C/T]GCCTTGCATGGTACA	55764
rs183337729	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502248	GGCATCCACTTTTCC[A/G]TGAGAATTCCTGCAC	55764
rs183414261	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129513885	AGGGGGCCCCAGAGC[A/G]CAGGCTGCCGCTCAG	55764
rs183614690	snp	A/G	0.00145661	0.0269478	synonymous-codon	IFT122	GRCh38.p7	3:129481574	TGCTATCGTCCTGCT[A/G]AAGCAGGCCACAGCT	55764
rs183615358	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455888	TTCATTGTCTTCAGG[C/T]TGAATAGGCTGAGGA	55764
rs183623890	snp	C/T	0.00755907	0.0610114	intron-variant	IFT122	GRCh38.p7	3:129495968	GGAGCCGCCAAGAAT[C/T]GGTGTCTTCAGGCAG	55764
rs183631523	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504172	GTTTTTGCATTTCTG[C/T]GGGTAGTTTTTTGGG	55764
rs183772767	snp	C/T	0.0189856	0.0955633	intron-variant	IFT122	GRCh38.p7	3:129453402	CACTGCCTCAGAGAA[C/T]GGGACAGCGAGTGGA	55764
rs183777200	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500804	GGCCACACTGGAAGG[C/G]CCTCCGATGCCAAAC	55764
rs183789713	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129468338	CAGCCTCAAGGGCTA[A/G]GAATGCTTTTCTTTT	55764
rs183825790	snp	A/C	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129470490	CAGGATGGTCTCAAT[A/C]TCCTGACCTCGTGAT	55764
rs183886651	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445124	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	55764
rs183898405	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457358	GGATAAAGAGCAAGG[C/T]CTCTGCTGTGTCCCT	55764
rs183924654	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471052	TAGTAGGATGACTTA[G/T]TAGTAGGCAGGAAAT	55764
rs183957934	snp	G/T	0.0592355	0.161582	intron-variant	IFT122	GRCh38.p7	3:129516478	CCCTGCACACACACA[G/T]GGAGACTGCCCCTGC	55764
rs183972237	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520646	TCTACATTTTAGCAA[A/G]TCATCTTATTGTCTG	55764
rs183978044	snp	G/T	0.00636936	0.0560724	intron-variant	IFT122	GRCh38.p7	3:129452573	AGAGGAAGAGCCATT[G/T]CAGAGGCCCTCAGGT	55764
rs183988967	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492401	TGTTGTGTGATAGCT[A/G]GGTGAGGCACATGGG	55764
rs184035564	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129453540	GATTTTGAGCTGCAT[A/G]GTTGTAGAGGCAGAA	55764
rs184061669	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129493557	CCCATGGGTCCATAG[C/T]CAAAAACTTGGTGGA	55764
rs184065863	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129468588	ACCTCAGGTGATCCA[C/T]CTGCCTCAACCTCCC	55764
rs184070620	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513375	TCCACTGGAGAAGAC[C/T]CAGAGCTCCTTGTTG	55764
rs184098537	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462039	AATCCCTCTCAGTGT[A/T]CCAGTTCCCTTATCT	55764
rs184104643	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496474	TGTTATGAAGTGACT[C/T]ATCAGCCATAACCTA	55764
rs184117141	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492879	GCTCAAGCGCAGTGG[C/T]ACGATCACAGCTTAC	55764
rs184179207	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129466754	GCGATTCACTTGCCT[C/T]GGCCTCCTGAAGTGC	55764
rs184192466	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488089	GTGCAGGATGGAGCA[A/C]ACAGGGTGGGCTGGG	55764
rs184205682	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129509825	TTTAGTGGGTAAACT[C/T]GAGAGTCCTCACACA	55764
rs184267866	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442138	CCAAATAAAACATTT[A/G]CTGGCCGAATGCAGC	55764
rs184272485	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512849	AGGTGGCAAAGCTGC[C/T]ATCAAAGAGGGAGGT	55764
rs184681164	snp	C/T	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129465727	GGCTCACTGCAAGCT[C/T]CGCTTCCCGGGTTCA	55764
rs184726139	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509302	ACCGTAGAATGGTTG[A/T]CATTGAGTTCTTCGG	55764
rs184825924	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441999	CCACCATGCAGGAAT[C/T]TGGCCTAGTGTGCTC	55764
rs184838113	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129448543	GGCCAGCGCCATGTT[C/G]CCCGTTTCTTTACTG	55764
rs184846396	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129487247	CTTGTTAAAGATGTC[A/G]TGGCCCAACTCAAGA	55764
rs184862282	snp	A/G	0.000313788	0.0125218	intron-variant	IFT122	GRCh38.p7	3:129461197	TCTTTGTGGTTTGCT[A/G]CATAGTAATCTACAG	55764
rs184862877	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129481461	GCACATGGGATTCCA[A/G]CGGCCTGGCAGTGGG	55764
rs184874852	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129503185	CAGTGCCTGCTGTTG[A/G]GCTGAGCTGCCTCTG	55764
rs184948552	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129505647	ATTTGAGTGCTCTCA[C/T]ATGGCAAGTGTCATG	55764
rs184974406	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486913	ATGCCTGCTGCCCCG[C/T]TAAAGGGAGCATTTA	55764
rs184986105	snp	A/G	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457981	CTGACCTCGTGATCC[A/G]CCCGCCTCAGCCCTC	55764
rs184991718	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129507818	CTGAGCTAGGGGTCC[C/T]GGGCATATCTAAAGA	55764
rs184993170	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129497997	TGTAGTATGTTCTTA[C/T]CAAAATCACCAAGCA	55764
rs185009123	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473903	AAATGGTTGTTGTTT[A/G]TAGTTGGTCCAGAGT	55764
rs185087194	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473289	GACAGAGCAAGACCT[A/G]TGCCCAAAAAGCAAA	55764
rs185139504	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470074	TTGAGTTAGGCTAAG[C/G]ACATTGGGAATGGTG	55764
rs185155263	snp	A/C	0.00597247	0.0543191	intron-variant	IFT122	GRCh38.p7	3:129455425	ATCCGCCCACCTCGG[A/C]CTCCCAAAGTGCTGG	55764
rs185511420	snp	A/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469347	TGTTGATTAGAGAGG[A/G]ACGTAATGACATCCT	55764
rs185522240	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514217	CTGGGCCTTGCCATC[C/T]GAGAAGTACACTCAC	55764
rs185622574	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448255	GAGGTTACGAGTAGA[A/G]GTTTAACAGGCGAAA	55764
rs185625091	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129455224	GTCGCCCAGGCTGGA[G/T]TGCAGTGGCGCGATC	55764
rs185655615	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518206	CCTCAGCCTTATAGC[C/T]CCCAGAAACAGCCAG	55764
rs185657225	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494226	TGTTTGTTTTTTTTT[A/T]GCAGAGATAGAGTCT	55764
rs185673123	snp	A/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129449726	CGGTTGAATGGAATT[A/T]GCAACAAATGCAATT	55764
rs185674320	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474688	CCGCTTAGGAAACTT[A/G]CAAGTTCATTTTGGC	55764
rs185676989	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459135	AGACTCAAATGTCAG[A/T]TTCTTTGTAAGGACT	55764
rs185681354	snp	C/T	4.94287e-05	0.00497111	intron-variant	IFT122	GRCh38.p7	3:129519101	TCCTTGACCAGATCC[C/T]TCCAGGCTCCCAGAT	55764
rs185689437	snp	C/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129499154	CTGCTGTCCCACTGT[C/T]GGATCAGGTTCTCAC	55764
rs185739984	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129465434	TGCTTTCTATGTCCA[C/T]GTGACTTTGAGAGTA	55764
rs185774771	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129498458	AGGCCCAAACTAGGC[A/G]GGGACAGCGGCTGCT	55764
rs185797076	snp	C/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129494808	CAGCTCTGTCTGACC[C/G]TGACCTGTTCCTCTT	55764
rs185818234	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470373	GGTTCACGCCATTCT[C/G]CTACCTCAGCCTCCT	55764
rs185818286	snp	C/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129455680	AATTTCTGAACCCCC[C/G]AAAACTTTACTATTA	55764
rs185820979	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129463332	CCTCCAGTTATCTCC[A/G]AACCCTGGTAACCAC	55764
rs185822301	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515183	GGTGCCCGGAGCATG[A/G]TAAATGGCTGGCTAA	55764
rs185832591	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129495854	CTTCATCAGTGACAG[A/G]GCTGGATGGCTGTGG	55764
rs185913915	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129445468	TGAAACAGGTATACA[A/G]TTGTTTTGAGGTTAA	55764
rs185936005	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129483971	GCGTGTGTTTTGCAG[A/G]GAGCCCAGCGTGGGG	55764
rs185946294	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129514993	CCAGCCAGCTTCCTT[C/T]TTTCACACATCCTCC	55764
rs185966505	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511090	TGTGGTTCAGCATCC[A/G]GGGCCCAGCAGAGCA	55764
rs186211205	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129444555	TGAGACAGAGTCTCG[C/T]TCTGTTGCCAGGCTG	55764
rs186217475	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129462856	ACCAGTGTGCCATGG[A/G]AGAGGCACAGCTCAG	55764
rs186236778	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129483120	CTCCCTCTACACATA[A/G]AACAGCTATATTGAT	55764
rs186256435	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129505009	TGGGCTGCACACAGC[A/G]TACAACAGCATCTGA	55764
rs186379544	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459841	TCACTGCAACTACAA[C/T]CTTCCAGGCTCAAAT	55764
rs186384103	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510454	GTCTTTGGCTTTCCT[C/G]AAACGAGACCCCCTC	55764
rs186404718	snp	A/C	0.00114149	0.023863	intron-variant	IFT122	GRCh38.p7	3:129477993	AACCTCTTGCTAGAA[A/C]TAGATATTTTTTTCT	55764
rs186414701	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129501291	GGGTCCTAAAGGCTG[C/T]TGATTCTTCTGGAAA	55764
rs186466972	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129443022	GTATTCCAATCAGGC[C/T]AGCATCTGCTGTAAC	55764
rs186478784	snp	C/T	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129482520	CCTCCTTGTTCTCAG[C/T]AGCAGAATCGATGGG	55764
rs186531298	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456979	GACTCTGAGGAAGAT[A/G]CTGTTCCTCTGTGTT	55764
rs186544357	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129490702	CGAATGCTCCTTTCC[C/G]TCTTGGCCACTGTGC	55764
rs186552955	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129497196	TTGCTTGAGCCCCAG[A/G]GGTGGAAGTTGCAGT	55764
rs186560742	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471162	AGCCTTTAATTGCGT[A/T]GCATCCTTATTCCTC	55764
rs186564100	snp	A/C	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129459542	CTATTTTTTTTTTCT[A/C]ACTCTTGTGTCCCTG	55764
rs186594478	snp	A/G	0.0142736	0.0832652	intron-variant	IFT122	GRCh38.p7	3:129499773	CAGCCCCTCAGGGCC[A/G]GGCCCTGCCTACCTC	55764
rs186646153	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129462303	GGTGGGATTAAAAAA[A/T]ATATAATATTAAGTA	55764
rs186657651	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453467	AGGGCCCTCTTGAAG[A/G]TTGTGATCATGAATT	55764
rs186659336	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479048	TGGATTTAGTTTTAC[A/G]TAGTTCTGTTGGAGG	55764
rs186663122	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504589	TGGAGCATGGAAAGA[C/T]CATTGGCCTTGGAGT	55764
rs186665616	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468543	AAGATAGGGTTTCCC[C/T]ATGTTGGCCAGGCTG	55764
rs186671638	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501708	TTTCCAGATGTGGCT[A/G]TAAAAGGTGTCTTTC	55764
rs186776586	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129516001	ACACACAGACACACA[C/T]GCACACACAGACTGC	55764
rs186815568	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477290	CAGAGTTCCCGGCCT[A/C]GCATAGTCATTCTAA	55764
rs186820382	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438203	AGCTAGAAACTTTTC[A/G]GATTAATCACTGAGT	55764
rs186846736	snp	A/G	0.000843833	0.0205233	intron-variant, missense	IFT122	GRCh38.p7	3:129519758	ACCCTGGTAGCTCAC[A/G]TGTGCTTCTCTTGGC	55764
rs186977677	snp	A/G	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129495995	GCAGGAGCCGGTCCT[A/G]CCGATCATGCAGGAC	55764
rs187161907	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129472843	TTCATTGACTCTTCT[G/T]CAACTTCCAATATTT	55764
rs187172945	snp	A/C	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129497778	TTGAGAAATATGTAC[A/C]TACACATTATGTGGG	55764
rs187267595	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129446417	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	55764
rs187300363	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129450877	AGGCGCCTGCCGCTA[C/T]GCTCAGCTAATTTTT	55764
rs187331376	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490052	TTTAAATATTGAGAC[A/G]GGGACTCACTGTGTT	55764
rs187403699	snp	A/C	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129491952	TTTACATGGTCCAAT[A/C]CCATGGATAAAGCCA	55764
rs187405331	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129451819	TTAGAATATTGACAC[A/G]TATTGTTATAAAAAC	55764
rs187408094	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129468176	GGTTAGTGCCTATGA[C/T]ATTTGCCACTCTTGG	55764
rs187411591	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511385	CTGAAGAAGTGTAGA[A/G]CAAAGTGAGTCCTCA	55764
rs187519883	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508787	GTGGTAGTTGGTTAG[C/G]AAGAGGTCAGGTGAA	55764
rs187528258	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486263	CAGTTGGTGTGGTTC[G/T]GGGAAGGAGCACCAG	55764
rs187528513	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129447282	GACATCAATCAGATA[C/T]ATTTAAGAAATACAT	55764
rs187534349	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129465098	ATGCACACATGTGTA[C/T]GTGTACATGTATATG	55764
rs187539316	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507193	CAGAGTCATGCTTAC[A/G]GTTTGAAAATTGTCA	55764
rs187580751	snp	A/G	6.5912e-05	0.00574035	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129467016	TCAGGGTAGTGAGGC[A/G]GAGGAGGAAGAACCA	55764
rs187632639	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129513156	CTCTTCTGTAGCCAT[C/T]GAGGGCCACAGTGGT	55764
rs187779702	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486937	GCATTTAATGTGCCA[A/G]TGAGGAGAGATGGCA	55764
rs187879408	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129460552	GGTGTGAGCCACTGG[A/G]CTCAGCTTCCTTCCT	55764
rs187896122	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493259	CCAGTTGGAAACAGT[A/G]AGGAAATAGCAAATG	55764
rs187960692	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440682	GCACGAAGCTGCTCA[A/G]GCTTCACAGTTCTTG	55764
rs188114620	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457431	TCCGTTCCATGATGA[C/T]TCCGCTCATTCCCTC	55764
rs188124643	snp	C/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129485325	CTCAGCTTCAGGCTA[C/G]AGCCCACTTCTTCTA	55764
rs188203356	snp	C/T	0.00993419	0.0697739	intron-variant	IFT122	GRCh38.p7	3:129498716	TACTTTTCTGACACA[C/T]GAGTGTTAATCATGG	55764
rs188207730	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129458930	GTTCATCTGACATTG[A/T]AGACTTTATCCCACC	55764
rs188209648	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474356	TAAATTGAATATTAG[C/T]TTAATAATGTTAATC	55764
rs188214854	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518535	CCCATCTCTGCCACC[C/T]AGGCTCCCTCAGGTG	55764
rs188265730	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502453	TTAGGAGATAATTGT[G/T]TCTATACCCTGCTGG	55764
rs188269752	snp	G/T	1.64735e-05	0.00286993	missense, intron-variant	IFT122	GRCh38.p7	3:129460877	CTGTGATGTCTTCAT[G/T]GCACCTCCATCTTCC	55764
rs188337505	snp	C/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504235	GGCAAAATATGATGT[C/T]CCTAATGGATTCAGC	55764
rs188402857	snp	C/T	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129506502	GGTTTAATGATGCTG[C/T]CTATTATTACTGGAT	55764
rs188407094	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464483	AAGTTTGATCCTCTG[A/G]CTTTATGTCAGGACC	55764
rs188486632	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129499380	TGTAAGTCATTTTGT[C/T]TGTGTAAGTTTAGGG	55764
rs188500852	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129519397	GCGCAGGTCTGTGGA[C/T]AGGGAGGCAGCTTCA	55764
rs188519806	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441297	TAAAGCATGCCGTCT[C/T]TCCTCATCTCACACG	55764
rs188560937	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129481112	TAAATGATAGCTATC[A/T]TGATCACTATCATCA	55764
rs188702268	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129466101	GGTGTGAGCCACTGT[A/G]CCTGACCCTATATGC	55764
rs188764809	snp	C/T	0.0197687	0.0974348	intron-variant	IFT122	GRCh38.p7	3:129470500	TCAATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	55764
rs188822902	snp	G/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129453798	CATGAAACTGAGATT[G/T]AAATTTATTTTAAAA	55764
rs188848490	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468612	ACCTCCCAAAGTGCT[A/G]GAATTACAAGCGTGA	55764
rs188858708	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513951	GACAGAGTGGGGTAC[A/C]CCCAGGGGCCTCAGA	55764
rs188865001	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129493796	AGGAGCATAATTTTC[C/T]TCTCTACAAAAGTAA	55764
rs188865459	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443081	GAGTACTTGCTATAG[G/T]CCACATGTCCACATG	55764
rs188923356	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452611	TGGCTGCTAGGAGCT[A/G]GATCAAAGAGAATCG	55764
rs188937042	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129492563	ATCCTCTCAGACTCC[A/G]GTAATCTGATAGTGT	55764
rs188968857	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449751	GCAATTCGTAGTTAT[A/T]CTTTTTCTCCTCAGT	55764
rs188988637	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129489468	AACAAGGGAAGTGAT[C/T]GTTGTGTAACAATGA	55764
rs189000680	snp	A/T	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466910	GGGAGAGTTTCTGGA[A/T]GAACAGAGAGAATGA	55764
rs189002089	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510286	GGCATTTCTTTCCCT[C/T]TAATCTGTGCTGACT	55764
rs189033157	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129455934	GGAGGAGGAAGAGGG[A/G]TTGGTGATGCTGTGC	55764
rs189052605	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129465505	AGATGGAGTCTCGCT[C/T]GGTTGCCCAGCCTGG	55764
rs189210095	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512177	TATGGCGCTCAGCAC[A/G]CAGTAGGAGTAGGTG	55764
rs189210822	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481888	GGCACAAGCCGCAGG[A/G]CCTGGACCGGCCTCT	55764
rs189212692	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129442327	CCAAATTATTCTAGA[C/G]ACAGGTCAGTGGTTG	55764
rs189257061	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129515120	TTCCCCCTTTCCCAC[A/G]GGTAGTTGTGAGGCT	55764
rs189352833	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448267	AGAAGTTTAACAGGC[A/G]AAAGAAAGAGAAGAG	55764
rs189483085	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462063	CTTATCTAAAAGGAG[C/T]ATGCTACTCACTGTG	55764
rs189621493	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442080	TGGCCTAATTTTTAA[A/T]TGTTAGCATCCACTC	55764
rs189623670	snp	C/G/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129481462	CACATGGGATTCCAA[C/G/T]GGCCTGGCAGTGGGC	55764
rs189625391	snp	A/C/G	1.64779e-05	0.00287031	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461259	CAATGTGTCTCCTAC[A/C/G]ATCCTATTACTCATC	55764
rs189636369	snp	A/T	0.00517822	0.0506191	intron-variant, stop-lost	IFT122	GRCh38.p7	3:129503610	GTCCATTTTAGAGTG[A/T]AAGCAAAGCCTTCAC	55764
rs189643838	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439206	GGATCTTATGAAATG[A/C]TATTGTTTACAATTT	55764
rs189649673	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459873	ATCCTCTTACTTCAG[C/T]TTCCCAAATAGCTGG	55764
rs189689936	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501478	CATCTTTTTCTTGTC[C/T]GATAGTAATTTTTTT	55764
rs189774917	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129487377	GCCAGCTATTTGCTG[A/G]GACAGGTCATTTGTC	55764
rs189792996	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129459445	TAGGCGCTCACCACC[A/G]TGCCAGGCTAATTTT	55764
rs189896168	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129462659	CGTTCTGGACCAGGG[A/G]AAAGGCAAAAAATAA	55764
rs189910722	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129495062	CTGCTCTGTCATCCC[C/T]ATGAGCCACAACTCT	55764
rs189914933	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129455643	GGGGTGCCACTGCCT[A/G]TGCAATAAAAAATCT	55764
rs189917199	snp	A/G	0.0142736	0.0832652	intron-variant	IFT122	GRCh38.p7	3:129504914	TGAGGCATGGTCTCT[A/G]CTGAGAATAGAAACT	55764
rs189921077	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470220	AACAGAGCTGAAGAG[C/G]AACATGGGGGTATGA	55764
rs190000332	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493990	GACTTATTTGCACAC[A/G]TCTGGGTGCTCAGCA	55764
rs190013420	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473726	CCCACTTCACTTTCC[A/G]GGTGCTGTGGTCCTC	55764
rs190035478	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474851	ACTTGTATCTGGAAT[A/G]TATAAAGAGCTATAA	55764
rs190041757	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509365	TCGATGATTGCTCTC[A/G]GTTGTTGTCAACTTC	55764
rs190048560	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467835	CACCCTGAGGTCATG[G/T]GGGCTGGGAAGTGGG	55764
rs190049393	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129518101	TCTGCCTCTCTTGGC[C/T]GCACTGTCCTCTGGG	55764
rs190064525	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490760	GCGCTTTAAGGAAAC[C/T]CAGATCTAGAGGGTG	55764
rs190177862	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482699	AAGCTGACCTGGGCT[C/T]GGGTCCTGCCTGCAT	55764
rs190278519	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458532	GAACTAGTTTTCTAA[A/G]GAATTCTCTCTGGGA	55764
rs190280574	snp	A/C	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129498174	AAGGAAGCTTTTAGA[A/C]CCAGCTTCAATGAAG	55764
rs190441762	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514797	CAGCCCTCAGCCTGG[C/G]CTCCCTTGCTCCTTG	55764
rs190568225	snp	A/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438251	TTCTGGGGGCACTTA[A/C]CATAAATTTGAGAAT	55764
rs190574855	snp	A/G	0.0189856	0.0955633	intron-variant	IFT122	GRCh38.p7	3:129455234	CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCATG	55764
rs190581089	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129470459	TTTAGTAGAGACGGG[A/G]TTTCACTGTGTTAGC	55764
rs190583498	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494549	CCTCCAATATGCTGC[A/T]CTTTCTAGAAAACAA	55764
rs190591240	snp	A/C/G	0.0343198	0.126438	intron-variant	IFT122	GRCh38.p7	3:129515446	GGGGGAGGAGGACAC[A/C/G]TGCCTGCCCCGGCCC	55764
rs190598707	snp	A/T	0.0126979	0.078662	intron-variant	IFT122	GRCh38.p7	3:129495882	TGGGTCTACACCAGC[A/T]CAATCCCTTCATTGA	55764
rs190701173	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129483187	AAAAGATTTAGTCAT[C/T]ATAAAAGATCCTAGG	55764
rs190713796	snp	A/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129467676	TCATTCTTCTCTTCA[A/G]TTGAGATTGCCTGTA	55764
rs190717415	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505280	TGCTGCCTATTTAGC[C/T]TTCTAATGGAAGTTG	55764
rs190722421	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129492257	CCTGTTTTAGGGGCA[A/G]CCCTTCTAACAGGCA	55764
rs190722996	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510647	CTCCCTGTCCTCTTC[C/T]TCACCTGGGGCATGG	55764
rs190730951	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468335	ACCCAGCCTCAAGGG[C/T]TAGGAATGCTTTTCT	55764
rs190739266	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511663	GCAGCCTCTAGGTAC[A/G]AAGACCAATCACTAA	55764
rs190813877	snp	C/G	1.64912e-05	0.00287147	intron-variant	IFT122	GRCh38.p7	3:129469453	CCAATTGCAGTCATG[C/G]CTGTTATATTTTCAT	55764
rs190838318	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445738	ACTTGACCTCTCTGA[A/G]CCATGGTATCCTCAT	55764
rs190877284	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484866	CTTTGCCTAGTTTCC[C/T]CCAACGGTAACAGTG	55764
rs190942802	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450975	TCCACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG	55764
rs190979713	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490385	CTAGATGGCAGAGAA[C/G]AGCTGCTGAGCTCCC	55764
rs191062893	snp	G/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129444640	CATTCTCCTGCCTCA[G/T]CCTCCCGAGTAGGTG	55764
rs191071992	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462926	CTAGATTTTCAGAAA[A/G]CATCATTGTTATTTT	55764
rs191120462	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129463350	CCCTGGTAACCACAA[A/G]TCTGTTCTCCATTTC	55764
rs191122342	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506062	ACCTTAGGAGTCACA[A/C]AACTTTGCCCTGGAA	55764
rs191257182	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129511210	CTATTCTCTCTGGGA[C/T]GTTACTTAGCTTCCC	55764
rs191363780	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457131	ATCCTCGTCTCTCAC[C/T]AGAGTAGGTGAAGAC	55764
rs191382825	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129497198	GCTTGAGCCCCAGAG[A/G]TGGAAGTTGCAGTGA	55764
rs191389068	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129471610	GTATGCAGCCCCAGA[A/G]CTCATGTTGTGGCCC	55764
rs191415623	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442090	TTTAAATGTTAGCAT[C/T]CACTCTGAAAAAAAA	55764
rs191420441	snp	C/T	0.000435643	0.0147523	missense	IFT122	GRCh38.p7	3:129481567	ATCTCTTTGCTATCG[C/T]CCTGCTGAAGCAGGC	55764
rs191426467	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461790	TCCTCCCTGAGGGGC[C/T]GAACACCTTGAGGAG	55764
rs191507056	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129453538	GCGATTTTGAGCTGC[A/G]TAGTTGTAGAGGCAG	55764
rs191528594	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493335	GCCAGCCCTTGTGCC[A/G]AGCTCAGTGGGCACA	55764
rs191538935	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468548	AGGGTTTCCCCATGT[A/T]GGCCAGGCTGGTCTA	55764
rs191548955	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129513157	TCTTCTGTAGCCATC[A/G]AGGGCCACAGTGGTA	55764
rs191676596	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477499	GGTCCCCCTGGGGGA[C/G]CCTATCTTTTTGAAG	55764
rs191685463	snp	A/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129452337	AGTAAAAAGGTAAAT[A/T]AAGTAGTATGCTGGA	55764
rs191687656	snp	C/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519962	TGGGGGCCCAGCAAG[C/T]GTGATGTGCCCTTGA	55764
rs191786693	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129455717	TACTGTTGACCAGAA[A/G]CCTTACCTGTTACAT	55764
rs191789951	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129456496	ATAAAAATTAGCTGG[A/G]CATGGTGGTGTGTGC	55764
rs191808916	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129485690	CCTCAAAAATAAATG[C/G]AGTTTGCTGCTCTCT	55764
rs191815269	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496435	ACCTGCCTTTTCTGG[A/G]AGTGTCAAAAGTGGC	55764
rs191931618	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459666	TTCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC	55764
rs191954750	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500144	GACTGACAAGGGAAC[C/T]AATAGTGCTTTTCTA	55764
rs192088086	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497827	CCTGATTAACGTGGC[A/G]TATTTTTGTTTACTT	55764
rs192101005	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129470501	CAATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC	55764
rs192122655	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129447008	GCCTGGGGCATTTGA[A/C]AAATCTTTGTAATAT	55764
rs192128912	snp	C/T	0.000773924	0.0196561	intron-variant	IFT122	GRCh38.p7	3:129464619	TCCCCATGCCTTTTG[C/T]TGGTTGTGTACACAG	55764
rs192135696	snp	C/G/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129516063	CTGCACACACACACA[C/G/T]AGACTGTCCCTGAAC	55764
rs192248408	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441369	CCTCTCTTTTGTGTT[C/T]GGCACTAGTGGTAGC	55764
rs192283193	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129468378	TGACAGAGTCTGGCT[C/G]TGTCACCTGGGCTGG	55764
rs192317015	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512549	GAGAACTCACCCTCC[C/T]GCTGCTGTTTGGCTA	55764
rs192371213	snp	A/C	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129465364	TACAGACGTCCCTAA[A/C]GCCTAGAGATACACA	55764
rs192387327	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486283	AGGAGCACCAGCTTT[A/C]AGTCCTGACTCTGCC	55764
rs192387651	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129447475	TTATTTGCAGAGGAA[A/G]CCTTCGGGTACTAGG	55764
rs192403775	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507595	ACTGTTGCCTGGCCC[C/T]TCCTCCTGGGGCCAG	55764
rs192442956	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129448490	AAAGCTGGCCACCCC[C/G]ACCCTAATCTTTTAT	55764
rs192453575	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486984	CACTTGGAAGCAGCC[A/G]TGTTTTGCTCTGAGA	55764
rs192523942	snp	A/C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503982	TGTTTCCTTAGGTGT[A/C/T]GCCCGCAATTAAAAG	55764
rs192562093	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129460668	TGCTTCTTAGCTATT[A/G]TGAATAATGCTGCTA	55764
rs192564683	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501792	GTCTATGCCACCTTT[C/T]CCTAAAAACGTGTCC	55764
rs192700828	snp	A/C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453369	GAGAGTTGAAGAGAA[A/C/G]GGGAAAAAGTGTAAA	55764
rs192705342	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492600	AGTTTCCCAAATGCA[C/G]ATGAGCTGAGCTCCA	55764
rs192768348	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465572	ACCTCTCGGGTTCAC[A/G]CAGTTCTCCTGTCTC	55764
rs192778642	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129509288	TCAAATGCCAAACAA[C/T]CGTAGAATGGTTGAC	55764
rs192816430	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440823	TATGAAAACCAGTGT[C/T]ACTTGCTCTAAATGT	55764
rs192828615	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479247	GAAAACAGAGACCCC[A/G]TCTCCACCAAAAAAA	55764
rs192892515	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129473204	AACTCTGTAGGCTGA[A/G]GTGGGAGTATTCTCA	55764
rs192964370	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481242	CTGCAGTTTGGGTAA[C/T]GTCATCAACAAATCC	55764
rs193035808	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498384	CAGGGTTTCCAGCTT[C/T]GTGCTGGCATAGAGA	55764
rs193089802	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457505	TTCCATCCATGTGGA[C/T]GGGTCTGTCTCCTCT	55764
rs193183329	snp	C/T	3.29815e-05	0.00406075	missense	IFT122	GRCh38.p7	3:129502755	AGGCTGAGCGCGAGC[C/T]CCTGCTGCTGTGCGC	55764
rs193222515	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129473811	ACCCTTAAAAAAATG[A/G]GAAGTTCACCTAGTG	55764
rs193225253	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129518182	AGGAGCAGTGCCAGC[C/G]CCACATCCCCTCAGC	55764
rs199499056	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476637	TCTCCAGAGAGCTGG[A/G]AATTGACAGTTCTCT	55764
rs199547061	snp	G/T	0.220246	0.248223	intron-variant	IFT122	GRCh38.p7	3:129454515	ATGGTAGTCATATTT[G/T]TGTGTGTGTGTGTGT	55764
rs199559551	in-del	-/TTACTTCCT			intron-variant	IFT122	GRCh38.p7	3:129460424	AGCATGTGTCAGAAT[-/TTACTTCCT]TTTTTTTCTTTATTA	55764
rs199582542	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129489857	AAAAAAAAAAAAAAA[C/T]AATTCAGAGGAGGGA	55764
rs199608976	snp	C/G	5.12965e-05	0.00506415	intron-variant	IFT122	GRCh38.p7	3:129514381	GTCCTTAACCCTGTT[C/G]ACGGCAGGAAAATAC	55764
rs199612057	snp	A/G	1.65007e-05	0.00287229	intron-variant	IFT122	GRCh38.p7	3:129461346	CCTGGAATAACTGAA[A/G]ATCTGGGCTAAAAAT	55764
rs199620413	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486542	TTAAGAAAAGCTTTC[A/G]GGAGTTTGAGAAAGC	55764
rs199622112	snp	A/C/G	8.26366e-05	0.00642749	missense	IFT122	GRCh38.p7	3:129514432	AGCAAGGCCCTCGGT[A/C/G]CCTACAGGCTGGCCC	55764
rs199672717	snp	C/T	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479827	AGCGGAGTGAAGGAG[C/T]GGGAGTGGCAGATGG	55764
rs199675691	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516977	TACACACACACACAC[-/AG]AGACTGCCCCTGCAC	55764
rs199736837	in-del	-/AAAAAC	0.0134861	0.0810011	intron-variant	IFT122	GRCh38.p7	3:129445329	AGACTCCACCTCAAA[-/AAAAAC]AAAAACAAAAACAAA	55764
rs199742667	snp	C/T	0.24059	0.249823	intron-variant	IFT122	GRCh38.p7	3:129495398	TTGTAAAGGCTGCTT[C/T]CTGCCCATGGCTGCA	55764
rs199758084	in-del	-/TGC			intron-variant	IFT122	GRCh38.p7	3:129487372	CTATTGCCAGCTATT[-/TGC]TGGGACAGGTCATTT	55764
rs199806189	snp	A/G	0.00199792	0.0315431	synonymous-codon	IFT122	GRCh38.p7	3:129483520	AGCTTGGAACACCCA[A/G]TGTGAGGACATGCTC	55764
rs199806683	in-del	-/G			downstream-variant-500B	IFT122	GRCh38.p7	3:129520775	AGGGGTGGGGGAGCA[-/G]GGGGTTTTTTTGTTT	55764
rs199844809	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129494213	TTTTTGTTTGTTTGT[-/TG]TTGTTTTTTTTTTGC	55764
rs199856807	snp	A/G	4.94189e-05	0.00497062	missense	IFT122	GRCh38.p7	3:129499992	AAGGAGCCCAAAGCC[A/G]CCGTGGAGATGTACA	55764
rs199869854	snp	C/G/T	0.000642261	0.0179088	intron-variant	IFT122	GRCh38.p7	3:129517636	TGTGTGCGGCTGTGT[C/G/T]AGGGGTCTGGGGACA	55764
rs199879872	in-del	-/CACACG			intron-variant	IFT122	GRCh38.p7	3:129516630	CTGCACACACACACA[-/CACACG]GAGACTGCCCCTACA	55764
rs199886551	snp	A/G	0.000279999	0.0118288	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464696	ATCATCAGCATACGG[A/G]ACAAAAATGGCGAGG	55764
rs199898312	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459634	TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC	55764
rs199904095	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129517206	CCTACACACACACAC[-/AG]AGACTGCCCCTGCAC	55764
rs199927550	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129448898	GAGACAAGGTTTCAC[C/T]ATGTTGGCCAGGCTG	55764
rs199934614	snp	A/C/G			intron-variant	IFT122	GRCh38.p7	3:129496803	CCTCAGGCCCCACCA[A/C/G]AGACACCTAGAAGAT	55764
rs199960077	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457517	GGATGGGTCTGTCTC[C/T]TCTCTACATCTGGCT	55764
rs200105122	snp	C/G	0.000298993	0.0122232	intron-variant	IFT122	GRCh38.p7	3:129514587	TTGGGCAGGTGGCTT[C/G]TCCTCTCCCTTGAGG	55764
rs200111278	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129460440	TACTTCCTTTTTTTT[-/C]TTTATTATTATTTTT	55764
rs200245900	snp	A/G	9.88354e-05	0.00702908	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504372	TGACATCTACATGCC[A/G]TATGCTCAGTGGCTA	55764
rs200259631	in-del	-/TTTTG			intron-variant	IFT122	GRCh38.p7	3:129459308	TTTTGTTTTGTTTTG[-/TTTTG]AGACAGAGTCTTGCT	55764
rs200285547	snp	A/G	0.000574295	0.0169357	intron-variant	IFT122	GRCh38.p7	3:129502910	CAGGCCTCATGGGCT[A/G]GGGCCCCACCTGAGC	55764
rs200300634	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443478	TCAAGCAGGGGCTAG[A/G]TGGCCATCTATAAGG	55764
rs200365796	snp	G/T	4.95462e-05	0.00497701	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507776	CGGTAAGGTGGCTGG[G/T]TCACCAGCACCTGAG	55764
rs200378115	snp	A/G	1.74592e-05	0.00295454	missense	IFT122	GRCh38.p7	3:129481602	GCTGTGCGCTGCTTG[A/G]ACATGAGTGCCTCCC	55764
rs200395338	in-del	-/GC			intron-variant	IFT122	GRCh38.p7	3:129516963	ACAGAGACTGCCCCT[-/GC]ACACACACACACACA	55764
rs200401678	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129467583	TCCCTTACCTTACCT[A/T]GCATTTTCTAGGATG	55764
rs200423795	in-del	-/TT			intron-variant	IFT122	GRCh38.p7	3:129478443	TTTTGTTTTATTTTA[-/TT]TTATTTTTTAAAAAA	55764
rs200451376	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129499250	ATGTTTGCTTGTTAT[C/T]TGTTCCAGGAAAGTA	55764
rs200453670	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129494686	TCCTAGCTGTGCTAA[A/G]TGTGTGTGTGTGTGT	55764
rs200474182	snp	A/G	4.94205e-05	0.0049707	missense	IFT122	GRCh38.p7	3:129495563	GGGCACGAGAACCTC[A/G]CGCTTGAAATGTACA	55764
rs200502635	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129467043	ACCAGAGGAAGAGGA[C/T]GACAGTCCCAGGGAC	55764
rs200529921	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129499268	TTCCAGGAAAGTAAC[G/T]GGGGCAAAGACAATG	55764
rs200539773	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129460416	TGTGTTGTAGCATGT[A/G]TCAGAATTTACTTCC	55764
rs200606803	snp	A/T	0.00161924	0.0284078	missense	IFT122	GRCh38.p7	3:129519583	CAAGGTGGCTCAGAG[A/T]TCGTGCCAGTGGTGG	55764
rs200661872	in-del	-/GA			intron-variant	IFT122	GRCh38.p7	3:129517104	CTGCCCCTGCACACA[-/GA]CACACAGAGACCGCT	55764
rs200677365	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456809	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	55764
rs200694449	snp	A/G	9.56732e-05	0.00691574	missense	IFT122	GRCh38.p7	3:129515510	TGCCCTTGTGCTACC[A/G]CTGCTCCACCAACAA	55764
rs200703087	in-del	-/GA			intron-variant	IFT122	GRCh38.p7	3:129516384	GCACACACACACAGA[-/GA]CTGCTCCTGCACACA	55764
rs200747264	snp	C/G/T	0.000395377	0.0140548	intron-variant	IFT122	GRCh38.p7	3:129519087	TGCTTCTGATTCCAT[C/G/T]CTTGACCAGATCCCT	55764
rs200774914	in-del	-/A/C	0.133438	0.221164	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438761	AAATGAAAAAAAAAA[-/A/C]CCCAAAAAAACAAAA	55764
rs200839602	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512496	CAGAGCACTTTCCTG[A/G]CAGAACCTTCCTCTC	55764
rs200840647	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520845	AAATACGTGGGTCCA[A/G]AGAAGATGGCAGGAG	55764
rs200844676	snp	C/T	0.000214163	0.0103458	intron-variant	IFT122	GRCh38.p7	3:129500089	TTTTGGTCCCTGCCC[C/T]GAGAAGCATTTGGCA	55764
rs200902776	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457519	ATGGGTCTGTCTCCT[C/T]TCTACATCTGGCTAA	55764
rs200913152	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454412	AAAAAAAAAAAAAAA[C/T]ACAAGTCATGTGACT	55764
rs200915373	snp	C/T	0.000494063	0.0157095	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476484	TGTGGACGTGTCAAG[C/T]GAAACCGGATTCCAA	55764
rs200967530	snp	A/G	0.00199793	0.0315432	intron-variant	IFT122	GRCh38.p7	3:129495415	TGCCCATGGCTGCAG[A/G]GGCCATTTCCTTTGC	55764
rs200990665	snp	C/T	0.00199792	0.0315431	intron-variant	IFT122	GRCh38.p7	3:129506400	TTCCTCCCTCCACCA[C/T]TCCTACAGCGTTCCA	55764
rs201027751	snp	C/G	0.49607	0.0441545	intron-variant	IFT122	GRCh38.p7	3:129516727	ACACACACACACACA[C/G]AGAGACTGCCCCTGC	55764
rs201077232	snp	A/G	0.000296477	0.0121717	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504348	TGAGAAGCATCCTGA[A/G]TTTAAGGATGACATC	55764
rs201122471	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516430	CCTGCACACACACAC[-/AG]AGACTGCCCCTGCCC	55764
rs201147770	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	IFT122	GRCh38.p7	3:129506410	CACCACTCCTACAGC[A/G]TTCCACAAGGCTGGG	55764
rs201176694	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129516382	CTGCACACACACACA[C/G]AGACTGCTCCTGCAC	55764
rs201176964	snp	A/G	0.00199792	0.0315431	intron-variant, missense	IFT122	GRCh38.p7	3:129467014	AGTCAGGGTAGTGAG[A/G]CAGAGGAGGAAGAAC	55764
rs201192197	snp	A/T			missense	IFT122	GRCh38.p7	3:129481549	TGAAGATCTTCGTGG[A/T]CAATCTCTTTGCTAT	55764
rs201194566	snp	G/T	0.00337387	0.0409335	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520153	TAGGGCTTCAGCCTG[G/T]TCTTACAGCTGTCTT	55764
rs201218755	snp	A/C/T	0.000115405	0.00759548	missense	IFT122	GRCh38.p7	3:129502833	ACCTGAAGATGGGTG[A/C/T]CCTCAAGTCCCTGGT	55764
rs201252917	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129476940	TGGGTCTGTGTCTTG[-/T]TTTTCTTTTTTTTTT	55764
rs201291306	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129468375	TTGTGACAGAGTCTG[G/T]CTCTGTCACCTGGGC	55764
rs201356347	snp	A/G	9.88517e-05	0.00702966	missense	IFT122	GRCh38.p7	3:129519122	GCTCCCAGATTCTGC[A/G]GCTAGTGGAGACCAA	55764
rs201377900	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129460450	TTTTTCTTTATTATT[-/A]TTTTTTTTTATGAAG	55764
rs201385711	snp	A/C	0.000793664	0.0199048	intron-variant	IFT122	GRCh38.p7	3:129452040	CTCTATAATAGCCTC[A/C]TCATTGTTCATTTTT	55764
rs201484056	in-del	-/TA			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475777	GTAATTGCACCACTG[-/TA]CACTCCAGCCTGGGT	55764
rs201494728	in-del	-/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457738	CAGGAATAGTTTTTT[-/G]TTTTTTTTTTTTTTT	55764
rs201528523	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129494687	CCTAGCTGTGCTAAG[A/T]GTGTGTGTGTGTGTG	55764
rs201536237	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516009	CACACACGCACACAC[-/AG]AGACTGCCCCTGCAC	55764
rs201556067	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517083	CCCTGCACACACACA[-/CA]GAGACTGCCCCTGCA	55764
rs201582620	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129472726	ACATTAGACCTTTTG[G/T]TACTGTTCTCCAAGT	55764
rs201586961	snp	C/T			missense	IFT122	GRCh38.p7	3:129495497	TTTCTGGCAGATGTG[C/T]TTTCCTACCAGGGGA	55764
rs201590142	snp	A/C/G/T	0.000264056	0.0114876	missense	IFT122	GRCh38.p7	3:129519682	AGGTGGCAATACTTC[A/C/G/T]GCTCACTGCTGCCTG	55764
rs201604137	in-del	-/ATTTTTTGT	0.281049	0.248064	intron-variant	IFT122	GRCh38.p7	3:129446390	CATCATGCTTGGCTA[-/ATTTTTTGT]ATTTTTTGTAGAGAC	55764
rs201630151	snp	A/G	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466981	ATCCCTTCCACTCTG[A/G]AGTCAGCAGTGTACA	55764
rs201643140	snp	A/G	0.000879135	0.0209474	intron-variant	IFT122	GRCh38.p7	3:129514578	GCAGCACCCTTGGGC[A/G]GGTGGCTTCTCCTCT	55764
rs201662098	snp	A/G	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129500037	CACGTCAAGGCCATC[A/G]AGATCTGTGGTGACC	55764
rs201664523	snp	C/G	0.000399281	0.0141238	missense	IFT122	GRCh38.p7	3:129502763	CGCGAGCCCCTGCTG[C/G]TGTGCGCTACCTACC	55764
rs201674500	in-del	-/T	0.0538939	0.155056	intron-variant	IFT122	GRCh38.p7	3:129460809	TTGCATGGTACATGA[-/T]TTGCTCAGCTTTCAT	55764
rs201753855	snp	C/T	0.000529293	0.0162593	intron-variant	IFT122	GRCh38.p7	3:129517450	CCAGCCCCCTCAGCC[C/T]TTTCTCTATGCCCTC	55764
rs201755623	snp	A/G	0.000457854	0.0151234	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520237	GCTGCCCCTACTGCC[A/G]CAGGTGCAAGGATGA	55764
rs201800117	snp	A/G			missense	IFT122	GRCh38.p7	3:129502769	CCCCTGCTGCTGTGC[A/G]CTACCTACCTCAAGA	55764
rs201806922	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129446240	TTTGTTTTTTTTTTT[C/T]CTGAGACAGAGTCTC	55764
rs201823275	snp	C/T	0.00199792	0.0315431	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129492185	TTTAGAGCTCATCAG[C/T]AGCATTGAGGTAAAA	55764
rs201824610	in-del	-/AA			intron-variant	IFT122	GRCh38.p7	3:129517237	ACACACACACACAGA[-/AA]CTGCCCCTGCACACA	55764
rs201825266	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456831	TGAGGCAGGATAATC[G/T]CTTGAACCCGGGAGT	55764
rs201833720	snp	A/C			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441764	CATTTTTCTTGAAAC[A/C]CAGCCGTATCAGTGA	55764
rs201858211	snp	C/T	0.000399281	0.0141238	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464661	ATGGTCAGTACCTGG[C/T]GCTGGGGATGTTCAA	55764
rs201891636	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504385	CCGTATGCTCAGTGG[C/T]TAGCAGAGAACGATC	55764
rs201911530	snp	C/G	0.00914312	0.0669923	intron-variant	IFT122	GRCh38.p7	3:129487885	GCTTGGGAGGACTCT[C/G]CAGAAGAGGTGACAT	55764
rs201970645	snp	C/G/T	8.37225e-05	0.00646955	missense	IFT122	GRCh38.p7	3:129483585	CCAGCACCTTCCCTG[C/G/T]GCACCGGCAGAAGCT	55764
rs201976052	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129442579	AAACAAAAAACTAAA[A/C]AAAAAAAAAAAAGAC	55764
rs202002444	snp	A/G/T	6.59667e-05	0.00574279	intron-variant	IFT122	GRCh38.p7	3:129519193	AGCTTTGAGGTGAGG[A/G/T]TGCCTCTCTGGGTGA	55764
rs202006807	in-del	-/GTGTGTGTGTGTGTGT			intron-variant	IFT122	GRCh38.p7	3:129465115	TGTACATGTATATGA[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	55764
rs202032451	snp	A/G	8.24069e-05	0.00641846	intron-variant	IFT122	GRCh38.p7	3:129469441	CCCTGTACAAATCCA[A/G]TTGCAGTCATGCCTG	55764
rs202074599	snp	C/T	0.000133496	0.00816885	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129467058	CGACAGTCCCAGGGA[C/T]GACAACTTGTGAGTG	55764
rs202080955	snp	C/T	0.000399281	0.0141238	intron-variant, missense	IFT122	GRCh38.p7	3:129466991	CTCTGAAGTCAGCAG[C/T]GTACAGTAGTCAGGG	55764
rs202099604	in-del	-/AGGA	0.0166325	0.0896639	intron-variant	IFT122	GRCh38.p7	3:129469716	GTGGAGCCTAGGAGT[-/AGGA]TAAACCCAGGTTGGT	55764
rs202155515	snp	C/T	0.000312956	0.0125052	intron-variant	IFT122	GRCh38.p7	3:129476649	TGGGAATTGACAGTT[C/T]TCTCACCCCGCAGGT	55764
rs202168923	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129442249	AAGAGTTAATTTTTT[A/T]AATCTGTTTAATTCA	55764
rs202175991	snp	A/C/T	4.94176e-05	0.00497059	missense, synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129492161	CATCAGAGTACAAGA[A/C/T]CTCCGATATTTAGAG	55764
rs202200755	snp	A/T	3.29587e-05	0.00405934	intron-variant	IFT122	GRCh38.p7	3:129495632	CCTGTCCCAGGCCCA[A/T]GCTCCAGCTTGGAGC	55764
rs202210457	in-del	-/AG/CA			intron-variant	IFT122	GRCh38.p7	3:129516754	TGCACACACACACAC[-/AG/CA]AGACTGCCCCTGCAC	55764
rs202221564	in-del	-/A	0.0611083	0.163768	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438721	ACCAGCCTGGAGAGC[-/A]ACAGTGAGATCCTCG	55764
rs207463707	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129512592	AGGGAGGCCCAGGGG[C/T]CCAGGCCAAGAGAAG	55764
rs267607191	snp	G/T			missense	IFT122	GRCh38.p7	3:129481546	TCCTGAAGATCTTCG[G/T]GGACAATCTCTTTGC	55764
rs267607192	snp	C/T	1.64727e-05	0.00286986	IFT122	3	allele_origin=T(germline)/C(germline)	3:129476463	TTGGGGAGCAGAACT[C/T]CTGGGTGTGGACGTG	55764
rs267607193	snp	C/G			upstream-variant-2KB, missense, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440351	GGCCGTGTTGACGTG[C/G]AGAGATAAAGCCGAG	55764
rs367569488	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129442888	AGCTGAAAACTCTAT[A/T]TTTCTACCCGAAGAT	55764
rs367576490	in-del	-/AT	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129465091	CATGTGCATGCACAC[-/AT]GTGTACGTGTACATG	55764
rs367584240	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129478632	TATTTTTAGTAGAGA[C/T]GCGAGGCTGTACTTT	55764
rs367595274	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129509611	ATAAACAGTAAGTAA[G/T]AACTCATTAGCAAAA	55764
rs367619284	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499772	TCAGCCCCTCAGGGC[C/T]GGGCCCTGCCTACCT	55764
rs367641579	snp	A/G	3.29468e-05	0.00405861	intron-variant	IFT122	GRCh38.p7	3:129476659	CAGTTCTCTCACCCC[A/G]CAGGTGGTCGGCTGC	55764
rs367654095	snp	C/T	3.29468e-05	0.00405861	intron-variant	IFT122	GRCh38.p7	3:129488249	TTTCCCTTGATGAAA[C/T]CCTGCAGTCCGCTCC	55764
rs367704478	snp	A/G	9.55064e-05	0.00690971	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440328	GCCGTAAGGGAAGCC[A/G]TGATGAGGGCCGTGT	55764
rs367713699	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465903	CGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	55764
rs367834133	in-del	-/TG/TGTGTG			intron-variant	IFT122	GRCh38.p7	3:129454513	CATGGTAGTCATATT[-/TG/TGTGTG]TGTGTGTGTGTGTGT	55764
rs367855699	snp	A/G	1.64735e-05	0.00286993	splice-donor-variant	IFT122	GRCh38.p7	3:129476507	GATTCCAACTATGTG[A/G]TAAGAAGAGAAAGTT	55764
rs367859332	snp	C/G/T	8.23776e-05	0.00641739	intron-variant	IFT122	GRCh38.p7	3:129451873	AGGAATTCTGACTAA[C/G/T]AGATATCACATAGAT	55764
rs367891133	snp	C/T	3.84749e-05	0.00438588	synonymous-codon	IFT122	GRCh38.p7	3:129515562	CAACGTCTGCATCAA[C/T]TGCCGCCAGCCCTTC	55764
rs367977884	snp	A/C	1.68165e-05	0.00289965	intron-variant	IFT122	GRCh38.p7	3:129502902	GGGGAAAGCAGGCCT[A/C]ATGGGCTGGGGCCCC	55764
rs367998779	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447832	TTTATCATACTTAAA[A/G]TCTGTGTTGATATTA	55764
rs368011258	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471312	AGGGAGCAGATAATG[A/G]AGTATTTTCTCAGTT	55764
rs368021355	snp	C/T	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129487735	TCTGCTGAGGGAGGC[C/T]GATACAACCCACCAC	55764
rs368032371	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129459348	AGGCTGGAGTGCAGT[C/G]GCACGATCTCGGCTC	55764
rs368040713	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493113	TTGAGCTACCATGCC[C/T]GGCCCTTAGACACTA	55764
rs368047180	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129515979	GAGCTGAGCAGAGGC[-/CA]CACACACACACAGAC	55764
rs368062325	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465698	CGGACTGCGGACTGC[A/G]GTGGCGCAATCTCGG	55764
rs368084126	snp	A/G	1.65143e-05	0.00287348	missense	IFT122	GRCh38.p7	3:129519622	CTGGTGCTGCGCTCC[A/G]TGAGCCGCCGGGATG	55764
rs368102876	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514793	GCCTCAGCCCTCAGC[C/T]TGGCCTCCCTTGCTC	55764
rs368113483	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444493	ACTACATTATGTTTT[C/T]GTAAGGATCAAATAA	55764
rs368120562	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490528	CAGGTTGAAGGAACT[C/T]GGAAACAGATTTATT	55764
rs368152801	snp	C/T	0.000115322	0.00759261	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507655	TTCCCCTCCCACCCG[C/T]TGCACACAGCAGATC	55764
rs368229661	snp	A/C	0.0154538	0.0865337	intron-variant	IFT122	GRCh38.p7	3:129496209	CATTGGGACGGCCCC[A/C]ATGAACCTTACTCCC	55764
rs368239028	snp	C/G	1.65296e-05	0.00287481	synonymous-codon	IFT122	GRCh38.p7	3:129519600	CGTGCCAGTGGTGGT[C/G]AGCCGGCTGGTGCTG	55764
rs368274438	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129516447	GACTGCCCCTGCCCA[C/G]ACACACAGAGACCGC	55764
rs368330760	snp	G/T	1.64735e-05	0.00286993	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476411	TCAGACAAGCAAGTA[G/T]CTCTTTTCACCAAGG	55764
rs368358931	snp	C/G	4.97203e-05	0.00498575	intron-variant, missense	IFT122	GRCh38.p7	3:129519781	CTCTTGGCCACTTTT[C/G]CCTTGCCCAAATGTC	55764
rs368409235	snp	C/T	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129499996	AGCCCAAAGCCGCCG[C/T]GGAGATGTACATCTC	55764
rs368505548	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129447509	CAGAAAGAATAGGTT[A/G]TAAAATGTTTCTTCT	55764
rs368530570	snp	C/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129515658	ACAGCCAGGCTCACT[C/G]CACTGCTCTCTGGCC	55764
rs368568826	snp	A/G	4.94915e-05	0.00497426	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507752	GTTACCATGCCATCC[A/G]TCGCCACACGGTAAG	55764
rs368574590	snp	C/T	4.0843e-05	0.00451883	missense	IFT122	GRCh38.p7	3:129515528	GCTCCACCAACAACC[C/T]GCTGCTCAACAACCT	55764
rs368598545	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518298	GAGGATGCACCAGGG[C/T]AGTTGTCCAGGGCAG	55764
rs368690956	snp	C/T	9.78497e-05	0.00699395	missense	IFT122	GRCh38.p7	3:129515509	GTGCCCTTGTGCTAC[C/T]GCTGCTCCACCAACA	55764
rs368734136	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129519272	TCAGCTAGCGCAGTG[G/T]TGGAGGAGGATTGGC	55764
rs368750069	snp	A/G	0.000455104	0.015078	missense	IFT122	GRCh38.p7	3:129481566	AATCTCTTTGCTATC[A/G]TCCTGCTGAAGCAGG	55764
rs368769201	snp	A/C	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129499308	TCTAGTTCAGGGCAC[A/C]GAATGTTTGCTGGTG	55764
rs368772409	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492816	CTATGCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT	55764
rs368785362	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438348	TCTCTGCAAATAAAT[A/G]AGGTAAAAGTTTTAC	55764
rs368786226	snp	A/G	8.23649e-05	0.00641683	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479815	TGCCTGTCCTTCAGC[A/G]GAGTGAAGGAGCGGG	55764
rs368851496	snp	A/C/G	0.000169453	0.00920323	intron-variant	IFT122	GRCh38.p7	3:129463676	TTCATCTTCCACACA[A/C/G]ACTCTCAAAATCCAA	55764
rs368851656	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129500924	CTAGTGCAGTAGAGC[A/G]GGAGGGAACTTGGTA	55764
rs368855664	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129480979	GATCACTTTGAGCCC[A/G]GGAGTTTGAGGCTGC	55764
rs368900068	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129450930	TTTCTCCGTGTTAGC[C/G]AGGATGGTCTCGATC	55764
rs368938355	snp	G/T	1.64784e-05	0.00287035	intron-variant	IFT122	GRCh38.p7	3:129469301	TATACTCATCAGCAG[G/T]CTGTGGCCCTTCATA	55764
rs368961022	snp	A/C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497291	TAATAAAATGCCTGG[A/C/T]CTTGGTGCCCCAGAG	55764
rs368991270	snp	A/T	0.000543456	0.0164752	intron-variant	IFT122	GRCh38.p7	3:129492217	ATGAAGCATTTTTCC[A/T]TCTCAAGAAGGCATA	55764
rs369000063	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490991	TTCGTAGTTGGAGAG[C/T]TCTTAGCTCTGGGAG	55764
rs369021690	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471498	GACTCTTGGGAACAA[A/G]TAACCACACTGCAGT	55764
rs369045084	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485371	CGAAACTCATGACTG[C/T]AAGACTTACTGGGGA	55764
rs369053694	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129481827	GGGGCCAAGCACATG[C/T]ACAGAGTCCCAGAGG	55764
rs369095286	snp	C/T	0.00014833	0.00861063	intron-variant	IFT122	GRCh38.p7	3:129512437	CTCTTATCCCTCCTC[C/T]GTCCCACCACCGTTC	55764
rs369095447	in-del	-/TTTTG	0.0640375	0.167087	intron-variant	IFT122	GRCh38.p7	3:129459284	GATACTGCATCTATT[-/TTTTG]TTTTGTTTTGTTTTG	55764
rs369102080	snp	A/G	4.94303e-05	0.00497119	intron-variant, missense	IFT122	GRCh38.p7	3:129467011	AGTAGTCAGGGTAGT[A/G]AGGCAGAGGAGGAAG	55764
rs369154504	snp	C/T	3.52622e-05	0.00419879	intron-variant	IFT122	GRCh38.p7	3:129515647	ACAGCCTGTGGACAG[C/T]CAGGCTCACTCCACT	55764
rs369210882	snp	G/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129512416	CATCTCTAAAGTGTA[G/T]CCTTTCTCTTATCCC	55764
rs369223361	snp	C/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129481743	CTTTGATTAGAGACT[C/T]TCCTCTAGCTTCCCA	55764
rs369229505	snp	C/T	4.94254e-05	0.00497094	intron-variant	IFT122	GRCh38.p7	3:129460820	ATGATTTGCTCAGCT[C/T]TCATTGTTGTCTAAG	55764
rs369241774	snp	A/G			utr-variant-3-prime	IFT122	GRCh38.p7	3:129520315	GCCTTGGGGTCTGCT[A/G]GGCTGTGAAGGAGAA	55764
rs369287435	in-del	-/T	0.00795532	0.062565	intron-variant	IFT122	GRCh38.p7	3:129508624	ATTATGATCAACACA[-/T]TTTTTGCCAATGAGA	55764
rs369289294	snp	C/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439511	CCTCCCGGCTCCCCC[C/G]CAGTCTCCCTAGTCA	55764
rs369326327	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129468493	GGGATTACAGACACG[C/T]GACACCACGCCGAAC	55764
rs369340161	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129496942	AGAATTTAGGGTTGG[C/G]AACCCCTGAGGCCTC	55764
rs369346055	snp	C/T	1.65108e-05	0.00287317	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478066	GCCATCTACAGAAAT[C/T]GATTGGCTATCCAAC	55764
rs369373741	snp	C/G	0.38286	0.211774	intron-variant	IFT122	GRCh38.p7	3:129465924	TGGGATTACAGGCGT[C/G]AGCCACCGCGCACGC	55764
rs369403278	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476166	GAGAGGCCTGTGTTC[A/G]CCATGGGATGACACA	55764
rs369414690	in-del	-/GTGTGTGTGTGTGT			intron-variant	IFT122	GRCh38.p7	3:129465115	TGTACATGTATATGA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	55764
rs369435682	snp	C/T	0.00755907	0.0610114	intron-variant	IFT122	GRCh38.p7	3:129444386	TTCCAGCTTCTTTAT[C/T]AGCCAGCTCTGTGAC	55764
rs369455330	snp	C/T	0.000153988	0.00877328	missense	IFT122	GRCh38.p7	3:129502725	GGTTGATCGACATCG[C/T]CCGCAAACTGGACAA	55764
rs369465881	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439168	GATGTAATTTGGGGT[A/C]AAATAATTTTGAGGA	55764
rs369482965	snp	G/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129491553	TTACATAAAGAGTTT[G/T]CCTTCCACAGACTTG	55764
rs369489464	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129505617	CTCCTTCTCTGAAGG[C/T]GGAGGATTAGGATCA	55764
rs369524752	in-del	-/C			intron-variant, frameshift-variant	IFT122	GRCh38.p7	3:129519828	CCCTGGGAGGAGGGG[-/C]CACATCCATGGCTCC	55764
rs369525803	snp	A/G	0.000263639	0.0114782	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458634	TCAGCTGACAAAAGC[A/G]TTATTATCTGGACAT	55764
rs369532906	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445224	CCAGCTACTCAGGAG[A/G]CTAAGGCAGGAGAAT	55764
rs369562461	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458379	ATGACAGCTACATGT[A/C]GTAGGCTCCCAATAC	55764
rs369696278	snp	A/G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480318	TGCGTTCCAGCATGT[A/G/T]TCCTAAAGAATGCTG	55764
rs369704793	snp	A/G	6.58892e-05	0.00573936	missense	IFT122	GRCh38.p7	3:129512313	TTCTCTCACTGCAGG[A/G]AGATCCGTTCAGTGT	55764
rs369729210	snp	C/T	6.60535e-05	0.00574651	synonymous-codon	IFT122	GRCh38.p7	3:129519699	CTCACTGCTGCCTGA[C/T]GCCTCCATTACCATG	55764
rs369742941	snp	A/G	3.32121e-05	0.00407492	intron-variant	IFT122	GRCh38.p7	3:129502662	GACATACGGCTTGCC[A/G]TTGACAAGACCCAGA	55764
rs369778316	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129479685	ATGGATACTGAATGT[A/G]TAGGTATTTTCTCCC	55764
rs369783323	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129466565	GCAGTGCAGTAGTGC[A/G]ATCTTGGCTCACTGC	55764
rs369827669	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445599	ACAGATTTGACATAC[C/T]TGGCAGTAATTCAAG	55764
rs369845656	in-del	-/GT			intron-variant	IFT122	GRCh38.p7	3:129471452	GCACACCTACTGTGT[-/GT]ACGAGGCACTGGATG	55764
rs369867116	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504378	CTACATGCCGTATGC[C/T]CAGTGGCTAGCAGAG	55764
rs369889330	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457344	TTCCCATTGCTTTAG[A/G]ATAAAGAGCAAGGCC	55764
rs369901139	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438230	GAGTAGGGCTATTAT[A/G]AAGATTTCTGGGGGC	55764
rs369902676	snp	A/C	0.000153988	0.00877328	synonymous-codon	IFT122	GRCh38.p7	3:129517509	CCTGGAGGAAGGGAT[A/C]ACTGATGAAGAAGCC	55764
rs369906058	in-del	A/GCG			intron-variant	IFT122	GRCh38.p7	3:129454559	TGTGTGTGTGTGTGC[A/GCG]TGTTTGAGTTCAAGT	55764
rs369931470	in-del	-/GAT			intron-variant	IFT122	GRCh38.p7	3:129446096	ACAGACTTTAAGTAT[-/GAT]AAGAAACATTTTACA	55764
rs369980749	in-del	-/TA			intron-variant	IFT122	GRCh38.p7	3:129504825	TTGCCTGAAGTTTCA[-/TA]GCTAGGAAGTGGCAG	55764
rs369988069	snp	C/T	1.64798e-05	0.00287047	intron-variant	IFT122	GRCh38.p7	3:129483478	CCCCACTGTCCCTGT[C/T]CCCCAGGAACCAAAC	55764
rs369997431	snp	C/T	5.16845e-05	0.00508326	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460968	AGGTGGGAGGATTGA[C/T]TGCTTGAGGCCAAGC	55764
rs369997478	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466508	TTCTTTTTTTTTTTT[C/T]TTTTTTTTTTTGAGA	55764
rs370054039	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511399	AGCAAAGTGAGTCCT[C/T]AGGAGTTCAGACCAA	55764
rs370107230	in-del	-/AC			intron-variant	IFT122	GRCh38.p7	3:129516404	CTCCTGCACACACAT[-/AC]AGAGACTGCCCCTGC	55764
rs370118655	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454582	GTTCAAGTTCAGAAT[A/G]ATGTTTTAGGGAGAC	55764
rs370161876	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515407	CTTGGCAGCCAGGCC[C/T]CAGGGGCCTGAAGCC	55764
rs370173989	snp	G/T	1.65064e-05	0.00287279	intron-variant	IFT122	GRCh38.p7	3:129499886	CAGAGTGTTTTTGTT[G/T]GTTGTGCTTCCTCAG	55764
rs370235408	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518831	TGGGCCCATCCCCTC[C/T]GTGCCTACCCGCAGT	55764
rs370254601	in-del	-/TT			intron-variant	IFT122	GRCh38.p7	3:129450012	TCTGAAATTTGACCC[-/TT]TTTTTTTTTTTTTGA	55764
rs370319739	in-del	-/CTT			intron-variant	IFT122	GRCh38.p7	3:129461731	GTTGCGGTTCTACTT[-/CTT]GTGCAATTTGTCGTC	55764
rs370404114	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501781	CTGTAAGGGCTGTCT[A/G]TGCCACCTTTCCCTA	55764
rs370405993	snp	C/T	0.00013185	0.00811835	intron-variant	IFT122	GRCh38.p7	3:129500120	GCATGTCATCACATG[C/T]CACCTCTTGACTGAC	55764
rs370415289	snp	A/G/T	0.000347633	0.0131797	missense	IFT122	GRCh38.p7	3:129502872	ACGTGGAGACCCAGC[A/G/T]CTGGGATGAGGTGAG	55764
rs370488054	snp	A/G	1.64732e-05	0.0028699	missense	IFT122	GRCh38.p7	3:129488270	AGTCCGCTCCCATGT[A/G]CCAGTACCTGGATAG	55764
rs370520115	snp	A/G	3.29478e-05	0.00405867	intron-variant	IFT122	GRCh38.p7	3:129488243	TCTTTTTTTCCCTTG[A/G]TGAAATCCTGCAGTC	55764
rs370626855	snp	A/G	4.97014e-05	0.0049848	intron-variant	IFT122	GRCh38.p7	3:129469467	GCCTGTTATATTTTC[A/G]TTTTCTGAGATTCTG	55764
rs370660486	snp	C/G	1.65288e-05	0.00287474	intron-variant	IFT122	GRCh38.p7	3:129458705	GGTGTACAGTATTAT[C/G]AGTTTGATGCTTATT	55764
rs370674028	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129459184	GGAACAGGTCTCTTT[C/T]GAGGCATTTCTCACA	55764
rs370686598	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129492975	TGCATGTGCCACCCC[A/G]CCTGATTAATTTTTT	55764
rs370693214	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129508540	GTGCAAAAGTAATTG[A/C]GGTTTCAGACTGAAT	55764
rs370706554	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129449401	TGACATATGGTAGTT[C/T]TTTGTGAAAGTGTCT	55764
rs370712569	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129472563	AGCAATTTGTTACAT[G/T]TTTCTTCTTGGTGTT	55764
rs370718087	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485739	GGAGCCAGAGGGGCA[A/G]CCTGGGGCTTCCTCT	55764
rs370722947	snp	A/G	1.79053e-05	0.00299204	missense	IFT122	GRCh38.p7	3:129483606	GGCAGAAGCTGCAGG[A/G]CTTTGTGGTCGGCTA	55764
rs370845379	snp	G/T	1.64743e-05	0.00287	missense	IFT122	GRCh38.p7	3:129495574	CCTCGCGCTTGAAAT[G/T]TACACCGACCTCTGC	55764
rs370899043	snp	C/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129506591	TTTTCCCAAGCCCCA[C/T]TCTGACACCAAGATA	55764
rs370954904	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129455381	TTTCACCATGTTGGT[C/T]GGCCTGATCTCAAAC	55764
rs371078903	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129498225	AGCTGGCCTAGGCTT[A/G]TGGCTCCCTCTCAGC	55764
rs371096007	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129447336	CAACTCAAAGTGAGG[A/G]CTTCCAGGCTATAGG	55764
rs371107052	snp	C/T	8.23866e-05	0.00641767	intron-variant	IFT122	GRCh38.p7	3:129479938	GTGAGTGCTCCCTCA[C/T]GTCTCCTGTCAGGCT	55764
rs371113865	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507399	GGAATAATCTGGGAG[A/G]GTGCAGTGAGAGATC	55764
rs371135558	snp	A/G	0.000169621	0.0092077	intron-variant	IFT122	GRCh38.p7	3:129514384	CTTAACCCTGTTCAC[A/G]GCAGGAAAATACTCT	55764
rs371139260	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129481896	CCGCAGGGCCTGGAC[C/T]GGCCTCTTTAACTTT	55764
rs371146624	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129495273	AAGCCTGCTTTTGTT[A/G]TCAAGCCTTCCCAGC	55764
rs371160205	snp	A/G	1.64738e-05	0.00286995	intron-variant	IFT122	GRCh38.p7	3:129449845	TTTTGGTTCCTAATT[A/G]TCTTTTTCCCTTGTC	55764
rs371251608	snp	A/G	3.30808e-05	0.00406686	missense	IFT122	GRCh38.p7	3:129514525	CTGGGTACCCTGACC[A/G]TCCGCGCCAAGCCCT	55764
rs371277209	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129442242	TGAGCATAAGAGTTA[A/T]TTTTTTAAATCTGTT	55764
rs371284757	in-del	-/CAGGTGGAAG	0.00264598	0.0362766	intron-variant	IFT122	GRCh38.p7	3:129476835	CCTTGGGAAGAGGGA[-/CAGGTGGAAG]CAGGTGGAAAGGGCT	55764
rs371292976	snp	A/G	0.000184751	0.00960943	intron-variant	IFT122	GRCh38.p7	3:129481499	CTTGTTGCCATGGTG[A/G]CTGACACTGTTTTCG	55764
rs371311619	snp	C/T	4.94368e-05	0.00497152	intron-variant	IFT122	GRCh38.p7	3:129464788	CCCTTCAAGGTACTC[C/T]TAAAGTTGTCCTCCT	55764
rs371325633	snp	A/T	8.23621e-05	0.00641672	missense	IFT122	GRCh38.p7	3:129500008	CCGTGGAGATGTACA[A/T]CTCAGCAGGAGAGCA	55764
rs371413088	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451970	GGGACACAAAGACAC[C/T]GTGTACTGTGTGGCA	55764
rs371454937	snp	A/G	8.24069e-05	0.00641846	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504301	CTTTATTAAGACTTC[A/G]TTTGCTCCTTCCCCC	55764
rs371504276	snp	C/T	0.38286	0.211774	intron-variant	IFT122	GRCh38.p7	3:129465921	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCA	55764
rs371556358	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466564	TGCAGTGCAGTAGTG[C/T]GATCTTGGCTCACTG	55764
rs371561455	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129483413	CTTTAAGAGGGTATT[C/G]GGCTGAAATGTGTGA	55764
rs371564287	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129509451	TTCTTGAACCACCAC[A/T]GCACTGTATGTTTGT	55764
rs371570973	snp	A/G	0.000247062	0.0111117	synonymous-codon	IFT122	GRCh38.p7	3:129506479	AAACAATGCCGTGGC[A/G]GAGAGCAGGTTTAAT	55764
rs371692313	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443217	CTAAGATTACAAAAT[A/G]AGTAAGTGGGGCTGG	55764
rs371703087	snp	C/G	0.000148279	0.00860914	intron-variant	IFT122	GRCh38.p7	3:129451875	GAATTCTGACTAATA[C/G]ATATCACATAGATAA	55764
rs371754567	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520120	CGTCCTGGCCCCAGG[C/T]GTAGGGCTGATGAGC	55764
rs371755754	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475332	TGTAGCAGTTCCTAA[A/G]AAAGGTTCAACGTAG	55764
rs371763617	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129504716	GCAGTGTATCTTCCC[A/G]TTTAATCCTCGCAAC	55764
rs371765365	snp	A/T	3.29511e-05	0.00405887	intron-variant	IFT122	GRCh38.p7	3:129476543	TGTGGGGCCATGGCT[A/T]GAAGAGGCACTGAGC	55764
rs371772807	snp	C/G			synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451937	CACCTCTGATGGCAC[C/G]TTACTTCAGCCCCTC	55764
rs371776414	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484079	TGTGAGAGAGAGGGG[A/G]GAGAGAGAATGAGTG	55764
rs371834870	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129462654	GGAAGCGTTCTGGAC[C/T]AGGGGAAAGGCAAAA	55764
rs371863942	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509632	ATTAGCAAAAAAACA[C/T]AAAGCGAGAAATGCC	55764
rs371871881	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474646	GTGTAGCACCTGTGA[G/T]GATGTGGAGGCCTGA	55764
rs371894257	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129503068	TCGTGGAGGGCCTTT[C/G]CACTTGTCCCTTCAT	55764
rs371901760	snp	A/G	3.32364e-05	0.00407641	intron-variant	IFT122	GRCh38.p7	3:129515476	CCTCGGGAGTCCGTG[A/G]CTGTTTTGTAGGAGT	55764
rs371937157	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444039	GGTGCAGACACTGCT[C/T]CAACATCTAATAATC	55764
rs371945981	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487501	AAGAAAGAGAAGTCG[C/T]TAGGAACTATTCATG	55764
rs371949471	snp	C/T			synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461258	ACAATGTGTCTCCTA[C/T]AATCCTATTACTCAT	55764
rs371964435	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129455404	TCTCAAACTCCTGAC[A/C]TCGTGATCCGCCCAC	55764
rs371965598	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474500	AACGAGAGAAGTGCA[A/G]TGGGATAGGCGAGCA	55764
rs371980576	snp	A/G			intron-variant, missense	IFT122	GRCh38.p7	3:129503524	CCCTGTTCCCTGCAG[A/G]GAAATCCATCCCCGA	55764
rs372010517	snp	C/T	5.6254e-05	0.00530319	synonymous-codon	IFT122	GRCh38.p7	3:129515598	CTCCGCCTCTTCCTA[C/T]GGTGAGTCCCTGCAT	55764
rs372031057	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129519471	TAGGAAGCAGGTCCT[C/T]TCTCACCACTGCCAA	55764
rs372035099	in-del	-/CTTC	0.495445	0.0475058	intron-variant	IFT122	GRCh38.p7	3:129459745	CTCCCTCCCTCCCTT[-/CTTC]CTTCCTTCCTTCCTT	55764
rs372043846	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129501692	AGCATGTTCTGCTTG[C/T]TTTCCAGATGTGGCT	55764
rs372131746	in-del	-/GATTGCTCCTG			intron-variant	IFT122	GRCh38.p7	3:129516684	CCCTGCACACACACA[-/GATTGCTCCTG]CACACACACACACAC	55764
rs372162926	snp	G/T	0.000469496	0.0153143	intron-variant	IFT122	GRCh38.p7	3:129502930	CCCACCTGAGCCCTG[G/T]GACACAGGCGGGTGG	55764
rs372177693	snp	G/T	1.6537e-05	0.00287545	intron-variant, missense	IFT122	GRCh38.p7	3:129519736	TCCTGCTTCCAGGTA[G/T]GTGGCCACCCTGGTA	55764
rs372209075	in-del	-/AAAC			intron-variant	IFT122	GRCh38.p7	3:129495210	TGAGGAATTTCCATT[-/AAAC]AAACAAAGGTTTGCA	55764
rs372220366	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129455179	ATTAAGTTTTTTTTG[-/T]TTTTTTTTTTTGAGA	55764
rs372233532	snp	A/C/G	0.00026359	0.0114773	synonymous-codon	IFT122	GRCh38.p7	3:129515529	CTCCACCAACAACCC[A/C/G]CTGCTCAACAACCTG	55764
rs372248047	snp	G/T	1.64746e-05	0.00287002	intron-variant	IFT122	GRCh38.p7	3:129492106	TTTTGAAGCCAAGAA[G/T]ACAGCTTATTTTATT	55764
rs372255149	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464708	CGGAACAAAAATGGC[A/G]AGGAGAAAGTAAAGA	55764
rs372291709	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129514073	GGGCCTGGCTGGCAG[A/G]TTTGGTGAGGCAGGA	55764
rs372292147	snp	C/T	0.000133211	0.00816014	intron-variant	IFT122	GRCh38.p7	3:129476835	CCTTGGGAAGAGGGA[C/T]AGGTGGAAGCAGGTG	55764
rs372307088	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129493386	TGACAGGAGCTCACA[G/T]CCTGCTAAGCCTCAT	55764
rs372346092	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465894	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	55764
rs372355939	snp	C/T	1.80097e-05	0.00300076	missense	IFT122	GRCh38.p7	3:129481573	TTGCTATCGTCCTGC[C/T]GAAGCAGGCCACAGC	55764
rs372361482	snp	C/G/T			intron-variant	IFT122	GRCh38.p7	3:129511952	TTCAGAGAAATGGAA[C/G/T]AATTACCAACTCCAG	55764
rs372363635	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129489890	AGGCATCTCTATGGA[G/T]GGAGCTTCCCTCTCC	55764
rs372375791	snp	A/T	0.38286	0.211774	intron-variant	IFT122	GRCh38.p7	3:129465925	GGGATTACAGGCGTG[A/T]GCCACCGCGCACGCC	55764
rs372381742	snp	A/C	0.0744748	0.178019	intron-variant	IFT122	GRCh38.p7	3:129442582	CAAAAAACTAAACAA[A/C]AAAAAAAAAGACAGT	55764
rs372388450	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443808	ATGATATATTTTAGG[A/G]AGGCAAATTTCAAGA	55764
rs372483083	snp	A/G	4.94662e-05	0.00497299	splice-donor-variant, intron-variant	IFT122	GRCh38.p7	3:129458678	CATTCTGAAGTACAC[A/G]TAAGTAACTTAGGTG	55764
rs372489108	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468604	CTGCCTCAACCTCCC[A/G]AAGTGCTGGAATTAC	55764
rs372497609	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129485113	GGACATGTTTGCTGC[C/T]TATAGCTTTTTTGTA	55764
rs372506085	snp	A/G	0.000145981	0.0085422	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520282	CAGCATCCTGGGGAC[A/G]GCCTGCACCCTCTGC	55764
rs372519478	snp	A/G	0.000197964	0.00994701	missense	IFT122	GRCh38.p7	3:129502749	TGGACAAGGCTGAGC[A/G]CGAGCCCCTGCTGCT	55764
rs372526517	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129516518	TGGAGACTGCCCCTG[C/T]GTGCACACACAGAGA	55764
rs372531693	snp	C/T			missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439831	CAGCCCAGTCGTGCC[C/T]ATCGAGCAGGGTCCG	55764
rs372532809	snp	C/T	6.58892e-05	0.00573936	synonymous-codon	IFT122	GRCh38.p7	3:129512338	CAGTGTCCATCGTCC[C/T]GAAACTCTTTTCAAC	55764
rs372545849	snp	C/T	0.00013233	0.00813311	synonymous-codon	IFT122	GRCh38.p7	3:129481670	CCTGGTGTATGACAT[C/T]GACACCAAGGAGCTG	55764
rs372554442	snp	C/T	6.64209e-05	0.00576247	intron-variant	IFT122	GRCh38.p7	3:129502661	GGACATACGGCTTGC[C/T]GTTGACAAGACCCAG	55764
rs372561450	snp	C/G	0.000153988	0.00877328	missense	IFT122	GRCh38.p7	3:129519602	TGCCAGTGGTGGTGA[C/G]CCGGCTGGTGCTGCG	55764
rs372574541	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129496004	GGTCCTGCCGATCAT[A/G]CAGGACGACATGGTG	55764
rs372593100	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458387	TACATGTAGTAGGCT[C/T]CCAATACATCTTTGT	55764
rs372597517	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481030	GTGAATAGCCACTGC[A/G]ATCAGCCTGGGCAAC	55764
rs372617533	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513786	ATGCGGGAGGAAGGG[C/T]AGGAGGGCCTGGGGG	55764
rs372702964	snp	C/T	0.000115379	0.00759449	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458595	ATTTTACAAACACTT[C/T]TAGGCAAGCGCTTTG	55764
rs372735871	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444642	TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGGTGGG	55764
rs372755342	in-del	-/A			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438723	CAGCCTGGAGAGCAC[-/A]AGTGAGATCCTCGTC	55764
rs372757203	snp	A/G	0.000153988	0.00877328	missense	IFT122	GRCh38.p7	3:129495462	AGAGGAAGAAGCGGG[A/G]AGAGACCAACAATGA	55764
rs372757997	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512854	GCAAAGCTGCCATCA[A/G]AGAGGGAGGTCACAA	55764
rs372799999	snp	C/G/T	3.29572e-05	0.00405928	intron-variant	IFT122	GRCh38.p7	3:129495613	GTATGCCAAGGTAAC[C/G/T]TACCCTGTCCCAGGC	55764
rs372800806	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129478565	GCTCAAGCGGTCTTC[C/G]TCCTGAGTAGCTGGC	55764
rs372821730	snp	A/G	1.65332e-05	0.00287512	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476322	TTCCTCAGATTGGAA[A/G]GGATCGGGCACTGAA	55764
rs372842084	snp	A/G	2.28355e-05	0.00337894	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439867	AGCAACGAGCCCAGC[A/G]CCGCAACGCCCAGGG	55764
rs372945368	snp	C/G	0.000115324	0.00759268	missense, intron-variant	IFT122	GRCh38.p7	3:129460915	GGCCTCCACAAAACA[C/G]TAAGAGTAACAGCCA	55764
rs372983894	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469401	AAGTTTCCTTCTACC[A/G]GCTGAGTGGAAAACA	55764
rs372993310	snp	A/C	1.64876e-05	0.00287116	intron-variant	IFT122	GRCh38.p7	3:129483456	CCCAGGGTGGTTCTC[A/C]CAGGATCCCCACTGT	55764
rs373040525	snp	A/G	0.000207978	0.0101954	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440400	CGGTTCGCGAAGAGC[A/G]GGAGGTCGAGTCCTC	55764
rs373041576	snp	A/C	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129517611	TATCCATGCCCTTGG[A/C]CAGAGCCTGTGTGTG	55764
rs373055341	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476255	AAAGCCCTTAATTGT[A/G]TTGCAATGGTTATGG	55764
rs373069533	snp	C/T			intron-variant, missense	IFT122	GRCh38.p7	3:129506805	AGAGCATATCTCTCC[C/T]CTGCTACCTGGGAGC	55764
rs373111458	snp	A/G	0.000164769	0.0090751	intron-variant	IFT122	GRCh38.p7	3:129512427	TGTATCCTTTCTCTT[A/G]TCCCTCCTCCGTCCC	55764
rs373114556	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129476945	TCTGTGTCTTGTTTT[-/C]TTTTTTTTTTTTTTT	55764
rs373126349	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129488082	GAGAGAGGTGCAGGA[C/T]GGAGCACACAGGGTG	55764
rs373152133	snp	C/T	4.95905e-05	0.00497923	synonymous-codon	IFT122	GRCh38.p7	3:129514428	GCAGAGCAAGGCCCT[C/T]GGTGCCTACAGGCTG	55764
rs373196573	snp	C/G/T	4.45782e-05	0.00472092	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439838	GTCGTGCCCATCGAG[C/G/T]AGGGTCCGGCTGCAG	55764
rs373212863	snp	C/G/T	4.94192e-05	0.00497067	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469349	TTGATTAGAGAGGAA[C/G/T]GTAATGACATCCTGG	55764
rs373243688	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129494265	TGACCAGGCTGGCCT[A/G]CAACTCCTGGGCTCA	55764
rs373258388	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482328	CTCTGTGCCCCGGGC[C/T]TGGTTGGCTTTCTGC	55764
rs373306639	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129448817	CTGCCTCAGCCTCTC[A/G]AGTAGCTGGGATTAC	55764
rs373313916	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485630	TGCCCCAAACTAGCT[C/T]TGCTTATTTTATTAA	55764
rs373326394	snp	C/G/T	3.29527e-05	0.00405898	missense	IFT122	GRCh38.p7	3:129519161	TCGGAGATGAGGACC[C/G/T]GTTCACAGCTAAGCT	55764
rs373367184	snp	G/T	3.29533e-05	0.00405901	missense	IFT122	GRCh38.p7	3:129483526	GAACACCCAGTGTGA[G/T]GACATGCTCTGCTTC	55764
rs373398441	snp	C/T	3.30524e-05	0.00406511	synonymous-codon	IFT122	GRCh38.p7	3:129502717	CCTCTCCAGGTTGAT[C/T]GACATCGCCCGCAAA	55764
rs373424989	snp	A/G	3.29489e-05	0.00405874	synonymous-codon	IFT122	GRCh38.p7	3:129479901	AAGAGAAGGCCTCTT[A/G]GTGGGGCTGAAGAAT	55764
rs373426335	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129476940	CTGGGTCTGTGTCTT[G/T]TTTTCTTTTTTTTTT	55764
rs373444436	snp	G/T	0.00636936	0.0560724	intron-variant	IFT122	GRCh38.p7	3:129514177	ATTAATGGAAACTAC[G/T]CTGTTTTTATCTTTG	55764
rs373454581	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129495170	CTATTCCGTCATAGC[C/T]TTGGAATACACAGGA	55764
rs373537903	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472791	TCTTTTCCCTCTGAT[C/T]TTCAGATTAGAGGAT	55764
rs373538975	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129518400	TCCCTTGCACTGACT[G/T]AGTCTGCAGGCCTGG	55764
rs373622965	in-del	-/TT			intron-variant	IFT122	GRCh38.p7	3:129450172	TCTTTCCCTTTTTAC[-/TT]TTTGAGACACCCATG	55764
rs373638458	snp	G/T	4.94539e-05	0.00497238	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478119	TGAGTTGTATTCAGA[G/T]GACTTATCAGACATG	55764
rs373652894	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129465902	CCGCCTCGGCCTCCC[A/T]AAGTGCTGGGATTAC	55764
rs373718093	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129485856	TAGGAAACACATTCT[C/G]AAGACAAAGGCTGTT	55764
rs373735641	snp	A/G	4.94262e-05	0.00497098	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507688	GCCCAGAAGGACACA[A/G]TGCTTGGCAAGTTCT	55764
rs373738589	snp	C/T	0.000115608	0.00760201	synonymous-codon	IFT122	GRCh38.p7	3:129502723	CAGGTTGATCGACAT[C/T]GCCCGCAAACTGGAC	55764
rs373779749	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473394	ATGGTTCACATTTTC[C/T]TGCTTTGGGGAATTT	55764
rs373786581	in-del	-/A			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458024	TTACAGGTGTGAGCC[-/A]ACTGTTCCCGGCCAG	55764
rs373788787	snp	A/G	0.000100642	0.00709303	intron-variant	IFT122	GRCh38.p7	3:129502898	GTGAGGGGAAAGCAG[A/G]CCTCATGGGCTGGGG	55764
rs373836204	snp	C/T	3.29489e-05	0.00405874	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451988	GTACTGTGTGGCATA[C/T]GCGAAGGATGGTAAA	55764
rs373854080	snp	A/G	6.59533e-05	0.00574215	intron-variant	IFT122	GRCh38.p7	3:129512449	CTCCGTCCCACCACC[A/G]TTCTTGTCTAATGGC	55764
rs373884266	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129517159	CCCCTGCACACACAC[A/G]GAGACTGCCTCTGCA	55764
rs373945657	snp	A/G			intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129503589	CTCACCCACCCACCC[A/G]TCATGGTCCATTTTA	55764
rs373997067	snp	C/T	0.000181233	0.00951753	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507637	AGACACTGTTTGACA[C/T]GTTTCCCCTCCCACC	55764
rs374021228	in-del	-/GTT	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129468774	TCAGTTTCAAAGACA[-/GTT]GTTTGTTTTCAGAGC	55764
rs374097927	snp	A/G	0.000263565	0.0114766	intron-variant	IFT122	GRCh38.p7	3:129476629	GCAGACTTTCTCCAG[A/G]GAGCTGGGAATTGAC	55764
rs374104529	snp	A/C	3.29674e-05	0.00405988	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504300	GCTTTATTAAGACTT[A/C]ATTTGCTCCTTCCCC	55764
rs374119180	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453524	TGTCTTTTTCTCCAG[C/T]GATTTTGAGCTGCAT	55764
rs374123480	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129472408	GGGCTCAAATGATTC[G/T]TCTGCCTTGGCTTCC	55764
rs374188891	snp	A/G	0.000247062	0.0111117	missense	IFT122	GRCh38.p7	3:129506518	CTATTATTACTGGAT[A/G]CTGTCCATGCAGTGC	55764
rs374207985	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129477961	TTTTAATTTCTCTGC[A/C]TTGCACCTTACATAA	55764
rs374210358	snp	A/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457841	CCTGGGTTCACTCCA[A/T]TTTCCCACCTCAGCC	55764
rs374235569	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129463234	TTCTGTTGTTTTATC[A/G]CATGTGTAGATTGCC	55764
rs374287484	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129495354	TAGGAAGGCCCAGGG[A/G]CCTCACTTGAAATAG	55764
rs374289603	snp	A/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438620	ACTGTTATTGAAAAA[A/T]GCTGGCAAGGCAAGG	55764
rs374303835	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449922	ACTGATTTTGGCTGC[C/T]GGAAGCAGATTACTG	55764
rs374308752	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129502120	CCTCTTTGGTCAGCA[C/T]GTTGGCCAGGAGGAC	55764
rs374313959	snp	A/G	2.5971e-05	0.00360345	missense	IFT122	GRCh38.p7	3:129483648	AGATCTTCTGCCTCC[A/G]TGTCTTCTCCATTTC	55764
rs374362619	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441731	TTTTCCCTAGGAATA[C/G]TCTTGTATTCTGTAC	55764
rs374367343	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	IFT122	GRCh38.p7	3:129499943	AGAAACAAAGATGCT[A/G]ATCACCAAACAGGCT	55764
rs374396013	snp	C/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129463530	GTATTCCAACCAATC[C/T]ATCTTCTTTTATATT	55764
rs374396112	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508716	AAAGCATTTTCTGCA[C/T]CCTGCTGGTTGTGGA	55764
rs374466670	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129492719	GGCTGAGAATATTGA[A/C]CTTGTCATCCAAACC	55764
rs374471559	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450910	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCGTGT	55764
rs374479969	snp	C/G	0.000195981	0.00989707	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440327	AGCCGTAAGGGAAGC[C/G]GTGATGAGGGCCGTG	55764
rs374500310	snp	C/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129512448	CCTCCGTCCCACCAC[C/T]GTTCTTGTCTAATGG	55764
rs374541698	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473882	TGCCTGCTTTTGGTC[A/G]CCCTGAAATGGTTGT	55764
rs374574041	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129488337	GGGTGTCACAGACAC[C/T]GATTGGCGTGAACTG	55764
rs374676705	snp	A/G	3.29489e-05	0.00405874	intron-variant	IFT122	GRCh38.p7	3:129451896	ACATAGATAATCTGT[A/G]TTTGTCTCTTTTGCC	55764
rs374796007	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509503	CGTTGTCGATGTTAC[A/G]AGTTGTCTCTGTTGC	55764
rs374836064	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468643	GCCATCACGGGCTGC[C/T]GCTTTTCTCTTGAAC	55764
rs374853657	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469987	CAGCTTTTTGGGACA[C/T]AAAAGAGGGTAACAT	55764
rs374868814	in-del	-/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129488576	AGGTGACACCCTTTC[-/T]AAGATTGCTTCTCTA	55764
rs374931836	snp	C/T	0.38286	0.211774	intron-variant	IFT122	GRCh38.p7	3:129465923	CTGGGATTACAGGCG[C/T]GAGCCACCGCGCACG	55764
rs374940598	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511750	CAGTTGAGGAACTCC[A/G]CATGTGTGCTCGTTT	55764
rs374965116	snp	A/G	0.000132374	0.00813445	intron-variant	IFT122	GRCh38.p7	3:129452043	TATAATAGCCTCATC[A/G]TTGTTCATTTTTCTC	55764
rs374970497	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487866	TGGGGTGGGGGCTTG[A/G]GGGGCTTGGGAGGAC	55764
rs375077150	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516286	CACAGATTGCTCCTG[-/CA]CACACACACACACAC	55764
rs375088773	snp	C/T	0.000445623	0.0149202	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439834	CCCAGTCGTGCCCAT[C/T]GAGCAGGGTCCGGCT	55764
rs375166736	in-del	-/GG			intron-variant	IFT122	GRCh38.p7	3:129516860	ACACACACACACAGA[-/GG]CTGCCCCTGCACACA	55764
rs375190200	in-del	-/ATCCAAACTCTAT	0.0130921	0.0798413	intron-variant	IFT122	GRCh38.p7	3:129450613	TCTCCAGTGTAAACA[-/ATCCAAACTCTAT]TAGTTTTTCTACATA	55764
rs375247834	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471223	AGATGTGTGTAGCCC[A/G]GCTTTTGGGCCATTT	55764
rs375273474	snp	A/T	3.49699e-05	0.00418136	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476268	GTATTGCAATGGTTA[A/T]GGATTCGGAAATGGT	55764
rs375277056	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487295	ACGCACATATGCACA[C/T]ATACACGCGTGCATA	55764
rs375315925	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129459246	TCAGTATTGCTCATC[A/G]GCCTGTAAGTTCCAT	55764
rs375501879	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439994	CTTTCCGGCCGCCCC[C/T]TCGGCTACAGCCGCC	55764
rs375504387	snp	A/T	1.65534e-05	0.00287688	intron-variant, missense	IFT122	GRCh38.p7	3:129519761	CTGGTAGCTCACATG[A/T]GCTTCTCTTGGCCAC	55764
rs375519779	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	IFT122	GRCh38.p7	3:129500036	GCACGTCAAGGCCAT[C/T]GAGATCTGTGGTGAC	55764
rs375544793	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503415	CTGTAAAGAATTAGC[C/T]AGGTCAGCGAGAAAG	55764
rs375595062	snp	A/C/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129483687	AGGTGCCGCAGGTAA[A/C/T]TGGGGGTGCCTGTCC	55764
rs375615520	snp	A/G	1.65206e-05	0.00287403	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478051	CTTGTCAAGAAGATT[A/G]CCATCTACAGAAATC	55764
rs375660621	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129466505	TTATTCTTTTTTTTT[A/T]TTTTTTTTTTTTTTG	55764
rs375738861	snp	A/T	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458556	TCTGGGAAATGCTGG[A/T]TTAAGATAAATGTAA	55764
rs375747713	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129476988	TAGGGATGCCAGTCT[C/G]CTTGAGGATCTCATG	55764
rs375819204	snp	A/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440589	GTGCCGCGCCTGAGG[A/T]GGTGGCGGGTGGAGG	55764
rs375838596	snp	G/T	3.29663e-05	0.00405981	intron-variant	IFT122	GRCh38.p7	3:129488227	GCTCTGAAAACAGTC[G/T]TCTTTTTTTCCCTTG	55764
rs375900149	in-del	-/ACACAC			intron-variant	IFT122	GRCh38.p7	3:129517195	ACAGAGACTGCCCCT[-/ACACAC]ACACACAGACTGCCC	55764
rs375945235	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129496669	TATTGTTCATCAGGA[C/G]TTGGACGAGCTCCTG	55764
rs375945385	snp	A/G/T	8.24455e-05	0.00642003	intron-variant	IFT122	GRCh38.p7	3:129483447	CTGACCAAGCCCAGG[A/G/T]TGGTTCTCACAGGAT	55764
rs375955924	snp	A/G	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129512283	GCTCTTGAAGAACTC[A/G]ATCCCTGTTTGCTTT	55764
rs375959003	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457288	GTAGTATGAAAATGC[G/T]AATCTGATCTATCAC	55764
rs375993159	multinucleotide-polymorphism	GTG/TTT			intron-variant	IFT122	GRCh38.p7	3:129468358	GCTTTTCTTTTTTTT[GTG/TTT]TGTGACAGAGTCTGG	55764
rs375996311	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444755	TCCATCTCTTGACCT[C/T]GTGATCTGCCTGCCT	55764
rs376018883	snp	A/G	0.000131778	0.00811614	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476436	CCAAGGATGGAGTGC[A/G]GCTTGGGACTGTTGG	55764
rs376246143	snp	A/T	5.04876e-05	0.00502407	missense, intron-variant	IFT122	GRCh38.p7	3:129460960	AAAGGCCAAGGTGGG[A/T]GGATTGATTGCTTGA	55764
rs376250638	snp	A/G	8.23635e-05	0.00641677	intron-variant	IFT122	GRCh38.p7	3:129517628	AGAGCCTGTGTGTGC[A/G]GCTGTGTGAGGGGTC	55764
rs376260287	snp	A/G	3.29527e-05	0.00405898	intron-variant	IFT122	GRCh38.p7	3:129469432	GGTATGTAGCCCTGT[A/G]CAAATCCAATTGCAG	55764
rs376279677	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129492816	TATGCTTTTTTTTTC[-/T]TTTTTTTTTTTTTTT	55764
rs376317354	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129519560	CCTCCTTCCCGCCCA[C/T]CCTGCAGCAAGGTGG	55764
rs376318080	in-del	-/TGT			intron-variant	IFT122	GRCh38.p7	3:129463476	ATCCATCTAAGTTGT[-/TGT]ATGTTTCAATTATTT	55764
rs376362722	snp	A/G	6.60567e-05	0.00574665	missense	IFT122	GRCh38.p7	3:129502724	AGGTTGATCGACATC[A/G]CCCGCAAACTGGACA	55764
rs376474450	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129459118	TTTACCCTGCAGATC[A/T]CAGACTCAAATGTCA	55764
rs376501284	snp	A/G	4.95274e-05	0.00497607	intron-variant	IFT122	GRCh38.p7	3:129461201	TGTGGTTTGCTGCAT[A/G]GTAATCTACAGTTGT	55764
rs376507116	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475735	AGGAAGATCGCTTGA[A/G]TCCAGGAGTTGAAGG	55764
rs376543459	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129461826	CCTGGCCACGGTCCC[C/G]TGCCAGCATTACAGC	55764
rs376549217	snp	C/T	0.000296467	0.0121715	missense	IFT122	GRCh38.p7	3:129506439	GGCGACAGAGAGAAG[C/T]GGTCCAGGTGCTGGA	55764
rs376558651	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129494430	GAGCCTGAGCTGTGT[A/G]CAGGTTTTTAGAATG	55764
rs376595844	snp	A/C/G/T	8.24075e-05	0.00641855	IFT122	3	allele_origin=G(germline)/A(germline)	3:129461309	CAGTGACTTTGGTAC[A/C/G/T]TTCTGATTCCTGATG	55764
rs376624826	snp	C/T	0.000307953	0.0124049	intron-variant	IFT122	GRCh38.p7	3:129512434	TTTCTCTTATCCCTC[C/T]TCCGTCCCACCACCG	55764
rs376626939	snp	C/T	0.000437904	0.0147905	intron-variant	IFT122	GRCh38.p7	3:129492076	TTGACTTCCCACCCC[C/T]AGCCAATCACCCACT	55764
rs376737617	snp	A/G	3.295e-05	0.00405881	synonymous-codon	IFT122	GRCh38.p7	3:129512410	CTCGGGCATCTCTAA[A/G]GTGTATCCTTTCTCT	55764
rs376806933	snp	A/G	1.65562e-05	0.00287712	missense	IFT122	GRCh38.p7	3:129481663	ACACTTGCCTGGTGT[A/G]TGACATCGACACCAA	55764
rs376811271	snp	G/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129481730	CAGGGACATCATCCT[G/T]TGATTAGAGACTCTC	55764
rs376819101	snp	G/T	1.65534e-05	0.00287688	intron-variant	IFT122	GRCh38.p7	3:129458717	TATGAGTTTGATGCT[G/T]ATTGAATAATTGCAG	55764
rs376934499	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129515612	ACGGTGAGTCCCTGC[A/G]TCCTGAGCATGTGGG	55764
rs377013509	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454763	AGGGCTCTTTGACCT[A/G]CAACACCATTAGGGC	55764
rs377078200	snp	A/T	0.000153988	0.00877328	intron-variant	IFT122	GRCh38.p7	3:129514372	GCCCCTGCTGTCCTT[A/T]ACCCTGTTCACGGCA	55764
rs377087422	snp	A/G	1.64743e-05	0.00287	intron-variant	IFT122	GRCh38.p7	3:129466886	AACTACTTACTGTCT[A/G]CAGCCGATGGGAGAG	55764
rs377100732	snp	C/T	0.000161313	0.00897945	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520273	GCCCATGACCAGCAT[C/T]CTGGGGACGGCCTGC	55764
rs377105452	snp	C/T	7.49279e-05	0.00612032	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520310	TGCCCGCCTTGGGGT[C/T]TGCTGGGCTGTGAAG	55764
rs377117661	snp	A/G	0.000153988	0.00877327	missense	IFT122	GRCh38.p7	3:129515539	AACCCGCTGCTCAAC[A/G]ACCTGGGCAACGTCT	55764
rs377136920	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440136	CACCATTGCTTTTGC[C/T]GCTTTTCTGGCTTTC	55764
rs377154840	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129494110	TGTTGACATGCACCT[C/G]CTGAGTGCCATAGAT	55764
rs377158883	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129512181	GCGCTCAGCACACAG[C/T]AGGAGTAGGTGCTCA	55764
rs377161382	snp	A/G	0.000347939	0.0131852	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504267	AAGTACAGTGTTTTC[A/G]TGGGGGCTGCAGGGG	55764
rs377161530	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129455321	GGGACTACAGGCACG[C/T]GCCACCATGCCTAGC	55764
rs377196719	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129460348	AGTTATTTCATTTCA[C/T]GTAATGTCCTCAAGG	55764
rs377200143	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129480963	GAGGCTGAGATAGGA[A/G]GATCACTTTGAGCCC	55764
rs377206266	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129510353	AAGAAGGACTCCTGA[C/T]AGGCTCTGTGCATGC	55764
rs377219797	snp	A/T	0.000153988	0.00877328	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476326	TCAGATTGGAAAGGA[A/T]CGGGCACTGAACTTT	55764
rs377247601	snp	G/T	1.65195e-05	0.00287393	intron-variant	IFT122	GRCh38.p7	3:129499880	CTGATCCAGAGTGTT[G/T]TTGTTTGTTGTGCTT	55764
rs377257739	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129515875	CAGAAAGAGAGTCCG[A/T]TGGCTTTGCATTCAG	55764
rs377268180	snp	C/T	1.65921e-05	0.00288024	missense	IFT122	GRCh38.p7	3:129495458	CAGGAGAGGAAGAAG[C/T]GGGGAGAGACCAACA	55764
rs377330861	snp	C/T	0.277067	0.24853	intron-variant	IFT122	GRCh38.p7	3:129488912	CACGTACCTTCATGG[C/T]GGGATTCATGGACTT	55764
rs377421786	snp	C/T	4.94678e-05	0.00497307	missense	IFT122	GRCh38.p7	3:129502835	CTGAAGATGGGTGAC[C/T]TCAAGTCCCTGGTGC	55764
rs377430415	snp	G/T	1.64749e-05	0.00287005	missense	IFT122	GRCh38.p7	3:129479909	GCCTCTTAGTGGGGC[G/T]GAAGAATGGACAGGT	55764
rs377487867	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503351	CCAGTTTTTTCCCTC[C/T]CTTCTCTGCCCCCAC	55764
rs377519355	snp	A/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503656	GACTGTTGTCTGCTC[A/T]CTGAACAGCTCCATT	55764
rs377519895	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129449255	ATAGGTCATTGATTA[A/T]AAAATACCATTGTTT	55764
rs377526400	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485725	GTGGCCGGCCAAGAG[A/G]AGCCAGAGGGGCAGC	55764
rs377531477	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449810	AAGTTTACTTTCCTG[A/G]CCATTAGCAGACTTC	55764
rs377532425	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469704	CAGCTAGTAAATGGT[A/G]GAGCCTAGGAGTTAA	55764
rs377534422	snp	A/G	0.00755907	0.0610114	intron-variant	IFT122	GRCh38.p7	3:129506261	GTTATTTAGAGAAGC[A/G]CCATCCCAGCAACGA	55764
rs377535652	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129486714	AGAAAATACAGTGAA[C/G]GTAATGATCATGCCT	55764
rs377588530	snp	A/G	1.70936e-05	0.00292344	intron-variant	IFT122	GRCh38.p7	3:129478247	TGTTGAAGGAGTTGG[A/G]CTGAATTCCATTTGT	55764
rs377593908	snp	A/G	0.000429312	0.0146449	intron-variant	IFT122	GRCh38.p7	3:129452032	TTTCCATTCTCTATA[A/G]TAGCCTCATCATTGT	55764
rs377607412	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129488128	GCAGGGTGCTGATTG[A/G]CGGCTGCAGGGCTGC	55764
rs377662681	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129514911	CTAGAAACCTCTGCC[C/G]TTTCTGGAACCAGGC	55764
rs377666553	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491338	CATTTTGAATGGGGC[A/G]ATAAATGGTGACAGC	55764
rs377683900	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453643	TGTATACAGATAAAT[A/G]ATTATGTACATTAAC	55764
rs377685213	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472409	GGCTCAAATGATTCT[C/T]CTGCCTTGGCTTCCC	55764
rs377690924	snp	C/T	9.88321e-05	0.00702896	missense	IFT122	GRCh38.p7	3:129506478	CAAACAATGCCGTGG[C/T]GGAGAGCAGGTTTAA	55764
rs377696382	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439965	TTGCGAAAGCGCCCC[A/C]GACGCCGCCGCTGCT	55764
rs386665770	multinucleotide-polymorphism	AC/GT			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457797	CTGGAGTGCAGTGGC[AC/GT]GATCTCGGCTCACTG	55764
rs386665771	multinucleotide-polymorphism	ATA/GTG			intron-variant	IFT122	GRCh38.p7	3:129462035	GCCTAATCCCTCTCA[ATA/GTG]TTCCAGTTCCCTTAT	55764
rs386665772	multinucleotide-polymorphism	CCT/GCC			intron-variant	IFT122	GRCh38.p7	3:129495355	AGGAAGGCCCAGGGG[CCT/GCC]CACTTGAAATAGCCA	55764
rs386665773	multinucleotide-polymorphism	GC/TT			intron-variant	IFT122	GRCh38.p7	3:129518135	CTTCATTCTTTGGCA[GC/TT]CCCGTGGTGCCCCCA	55764
rs397515567	in-del	-/G			frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476453	CTTGGGACTGTTGGG[-/G]AGCAGAACTCCTGGG	55764
rs397515568	snp	A/G			missense	IFT122	GRCh38.p7	3:129479917	GTGGGGCTGAAGAAT[A/G]GACAGGTGAGTGCTC	55764
rs397719625	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129508809	CAGGTGAATATTGCG[-/G]ATGAGGCAAAATTTT	55764
rs397731993	in-del	-/AG	0.375	0.216506	intron-variant	IFT122	GRCh38.p7	3:129470605	TCCAGCCTAGGCGAC[-/AG]AGTGAGACTCTGTCT	55764
rs397935692	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129442591	AACAAAAAAAAAAAA[-/A]GACAGTAGAACTAAA	55764
rs397951689	in-del	-/TTTTTTGTA			intron-variant	IFT122	GRCh38.p7	3:129446400	GGCTAATTTTTTGTA[-/TTTTTTGTA]GAGACGGGGTTTCAC	55764
rs397970427	in-del	-/G/GTGG/GTGTGT			intron-variant	IFT122	GRCh38.p7	3:129494709	TGTGTGTGTGTGTGT[-/G/GTGG/GTGTGT]TGTTGGGGACATCAC	55764
rs397972472	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129487759	CACCACTGCCCACGG[-/G]CTGTGCACGGCTTTG	55764
rs397991078	in-del	-/C	0	0	intron-variant	IFT122	GRCh38.p7	3:129487941	CCCCTCCCCACTCTG[-/C]CTCTGGAAAATACCT	55764
rs527241352	in-del	-/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129459666	TTCTTCCTTCCTTCC[-/T]TCCCTCCCTCCCTCC	55764
rs527274130	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456382	GGTGGCTCATGCTTG[C/T]GATCTCAGCACTTTG	55764
rs527300039	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449487	TCTGTTCATATCTGT[C/T]GGTGCCTGGCACCTA	55764
rs527321794	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501454	ACCTTGATGGATGTC[C/T]TACCACCCCATCTTT	55764
rs527336578	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450080	ACTTTTTAATAGGGA[G/T]GGAAATGGGCTATTT	55764
rs527387636	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489940	AGCAGGGAGGGAGAC[C/G]ACAAATCCCTAGAAT	55764
rs527439210	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502252	TCCACTTTTCCGTGA[C/G]AATTCCTGCACCCGT	55764
rs527470540	in-del	-/TTTTTTTTTTTTT			intron-variant	IFT122	GRCh38.p7	3:129466507	ATTCTTTTTTTTTTT[-/TTTTTTTTTTTTT]GAGACGGGGTCTCAC	55764
rs527498932	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129449173	TGCGTCTTCCTCCTT[C/T]GAATCCTGTTTTCAT	55764
rs527512184	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129477133	TGGTTGACCTGCATG[C/G]GTCTTCGTGGACCTT	55764
rs527540867	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520106	CTTGAGAGGCAGTGC[A/G]TCCTGGCCCCAGGCG	55764
rs527565152	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484894	GTGTGCATAGCTCTA[A/G]AGTGATCTTCCCACC	55764
rs527627787	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129499279	TAACTGGGGCAAAGA[A/C]AATGTGATGATTCTC	55764
rs527637907	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470867	GAGCTGCCACCACGC[C/T]TGGCTGGAGATGTGA	55764
rs527659647	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488744	CTGACTAGTAGCCTG[C/G]CACATCACAGGCACT	55764
rs527677674	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440789	TTCACATTTTACAAG[A/G]AAACTTTATTACTCC	55764
rs527716984	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441133	GCCTAAATCTATAAC[A/G]TAGCAGTCTGTTTTG	55764
rs527741750	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129454216	TCACTTTAGTCCTGC[A/T]TAAAGACATAAACAA	55764
rs527859682	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129506284	AGCAACGAAGCACTG[C/T]AGATGCTCCAATGAG	55764
rs527864738	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129518774	CTCCATCACAAGTGC[C/T]CGCAGACCCCCAGCA	55764
rs527901175	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462589	AGCTTGGGGCTCCAG[A/G]CAGGCTTAGTGGAAC	55764
rs527905698	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469585	CTTTATCCTATTTTA[G/T]TCTTATAAAACCCAA	55764
rs527928616	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513552	TGGGGGCTGAGCACC[G/T]GTACTCATCCTTTCC	55764
rs527934495	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506331	CAGCCCTGTGCAAGC[C/G]CCACAGAGCTCCATC	55764
rs528022692	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463219	GTGTATATTATATAG[A/T]TCTGTTGTTTTATCG	55764
rs528055811	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517206	CCCTACACACACACA[C/T]AGACTGCCCCTGCAC	55764
rs528096798	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468034	GCCTCCCCAAGAGGG[C/T]TCACTGGTGGGCTGG	55764
rs528115066	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511614	TTTGTAGACCCTCAC[A/C]CAGAAAATTCCTTAT	55764
rs528142799	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129512168	CAGTGGCTATATGGC[A/G]CTCAGCACACAGTAG	55764
rs528152524	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129514027	CTGGCAGGGTGAGAG[C/T]AGAGTGCCCTTTGTG	55764
rs528203441	snp	G/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129461167	TATTAAAATCTTCAG[G/T]TGTAGCCACTGAAAT	55764
rs528211764	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504987	CTCAAGAATTCTGTT[A/G]GTAAAATGGGCTGCA	55764
rs528216115	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499026	GAGGTATGCTGAGGC[C/T]GAAGGAACACAGGCC	55764
rs528277385	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455093	TTTTCCTCTTAGACC[G/T]GAAGATTGAGATACA	55764
rs528329340	snp	G/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129499523	GAACAGTCCTGTATT[G/T]ACCAAACTATGTGAG	55764
rs528330195	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447800	ACAGGCATGAGCACC[A/G]CACCCAGCCTAAAAT	55764
rs528383242	snp	C/T	3.29511e-05	0.00405887	missense	IFT122	GRCh38.p7	3:129488341	GTCACAGACACTGAT[C/T]GGCGTGAACTGGCCA	55764
rs528394547	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494890	GAGGGTCACTGAGAG[G/T]AATAAAGGGGCCATG	55764
rs528487457	snp	C/G	0.000228964	0.0106972	intron-variant	IFT122	GRCh38.p7	3:129459288	CTGCATCTATTTTTT[C/G]TTTTGTTTTGTTTTG	55764
rs528494472	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503841	CCATGGCTCATGTCC[A/G]GTTCTCCTGGCCTGA	55764
rs528541444	in-del	-/AG	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129503395	CTTCTCTCTGGTGTC[-/AG]GGGCTGTAAAGAATT	55764
rs528543172	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129445276	GGTTGCTGTGAGCCA[A/G]GATCCTGCTACTGCA	55764
rs528575102	snp	G/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129498490	TCCAAGCCCCTTCCC[G/T]TTGTCAGCTCCAGGG	55764
rs528585314	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129492170	ACAAGACCTCCGATA[C/T]TTAGAGCTCATCAGC	55764
rs528587111	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492620	GCTGAGCTCCATTCC[A/C]CAGAAATGGACCTGG	55764
rs528671501	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487327	ATGTGGCAGGAAGGG[A/G]CACAGAACCTGGAGT	55764
rs528673849	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446277	TCGCCCAGGCTGGAG[C/T]GTAGTGGCGCGATCT	55764
rs528701679	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129464213	GAGTATATCCCTTCC[A/G]TTCAGCATCTGTTGA	55764
rs528752418	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440102	TCTGGTTGCGCTGGC[C/G]CCTTAGGGGCTCCAG	55764
rs528781756	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129481327	TCTGCAGCCTCTGAT[A/G]AACCTCGCTTCTGGC	55764
rs528813480	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457979	TCCTGACCTCGTGAT[C/T]CACCCGCCTCAGCCC	55764
rs528836754	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129489195	GAGGGACGTGATGCC[C/T]GCCTTGGGTTAGATC	55764
rs528843087	snp	C/G	1.65299e-05	0.00287483	missense	IFT122	GRCh38.p7	3:129481675	TGTATGACATCGACA[C/G]CAAGGAGCTGCTTTT	55764
rs528915155	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505054	CAAGTATAGAACTTT[C/G]GCTGATGTTATTAAT	55764
rs528975353	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129444664	GTAGGTGGGACTACA[G/T]GTGTGCACCACCACG	55764
rs528987894	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499622	AAGTGTTGTTTAGCC[A/G]ATGAACAAATGCCCA	55764
rs529002061	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129494237	TTTTTGCAGAGATAG[A/G]GTCTGGCTATATTGA	55764
rs529021851	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462307	GGATTAAAAAAAATA[A/T]AATATTAAGTACTAG	55764
rs529030382	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447962	GAAGTCCATTCAGAC[G/T]GTTGGGGGGGCTTAC	55764
rs529048056	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503637	TCACTGAGAGGAGCC[A/G]TCTGACTGTTGTCTG	55764
rs529090638	in-del	-/C	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129461550	CAAAGGAAATGGTAA[-/C]AAGATTGGGAGGGCA	55764
rs529102293	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441199	CTTTGAAAATCATTC[A/G]GCATTGTTGTGAAGC	55764
rs529157209	snp	A/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129488784	GCGGCTTTTATTATC[A/G]GTGTAGTCACTGGCC	55764
rs529215206	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482953	TTGTGTCTGAGCCTA[C/G]AATCATACAAGTGTG	55764
rs529217787	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498930	TGTATTTTGGGTAAC[C/T]ACTCTGAAAAGAGGT	55764
rs529249169	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129447723	TCACCATGTTGGTCA[G/T]GCTGGCCTCAAACTC	55764
rs529255487	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492731	TGACCTTGTCATCCA[A/G]ACCCAATAGGCCTGC	55764
rs529302653	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453119	AAAGTTGATGATGTC[A/G]GAGAGGGGAGAGAAC	55764
rs529331781	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129509221	ATATTTTCATTTTCT[A/G]TCAGCTCATGAGGCA	55764
rs529341694	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439609	CTAGTAACTAAACCC[A/C/G]TGGGCTTCGAGGTTT	55764
rs529362901	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129499511	ATTGCTGTTTAGGAA[C/T]AGTCCTGTATTGACC	55764
rs529409750	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129487791	TGTGGGAACAGGCCT[C/G]TAACTGCGGCACAAC	55764
rs529454660	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440187	GGAGCAAGGCGCCCT[A/C/T]GCACTCAGCTTACCG	55764
rs529527122	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475016	TTTAATTAGCTGAGT[A/G]TGGTGGTATATGCCT	55764
rs529551394	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511655	AGCTTCTGGCAGCCT[C/G]TAGGTACGAAGACCA	55764
rs529576195	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482367	CGCCATTCTTTCTCT[C/G]TTTAGGTCTTTGTAG	55764
rs529615032	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129479665	GTCTACATTGGGTTA[C/G]ATAGATGGATACTGA	55764
rs529641334	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487810	CTGCGGCACAACCTG[C/T]GATCTGGACAAAGGG	55764
rs529648393	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445044	ATTGCCTGGGTTTGA[A/G]GCCGGATGCAGTGGC	55764
rs529772338	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515770	ACAAGGAGTCACTGT[C/T]GGTGTTCCCAGAGAT	55764
rs529787730	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129473247	CAAGGCTGCAGTGAA[C/T]TCTTACCACTGCACT	55764
rs529800338	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129473960	TGGTCCGATGGGAAC[C/T]AGTGAGCCATTTCCA	55764
rs529817221	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509991	GTGACCCTAGGTGGC[A/C]GCTATCCTTACTGCT	55764
rs529859878	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466388	CAGAGGACTTGGTGG[C/G]TCTAGGCTACCATTT	55764
rs529941091	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503902	GTCAGTGGGTCCATA[C/T]AGCACGAAGCCCACA	55764
rs529942363	in-del	-/CCTT			intron-variant	IFT122	GRCh38.p7	3:129459772	CTTCCTTCCTTCCTT[-/CCTT]TCTTTTCAGTCTTGC	55764
rs529944062	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498569	CAGGGTATACAATGC[A/G]CTTTCCTCCCCTTCT	55764
rs529978989	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129460026	AAGTACTGGGATTAC[A/G]GATACGAGCCACTGC	55764
rs530094100	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509138	CTTTTTGTCACACCT[C/T]ACATCTGATTGAGAA	55764
rs530138684	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508035	ATGACTCAGGGAAAC[A/T]CTGCATTAACCAGCA	55764
rs530168997	snp	A/C/G	0.000185787	0.00963634	intron-variant, splice-acceptor-variant	IFT122	GRCh38.p7	3:129456113	CCATTTTTCAAATAA[A/C/G]GAAATGAAAGCTCTT	55764
rs530212290	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502152	GGGAAGACTTCCTGC[A/C]GGCCTTTGTCCAGAG	55764
rs530227553	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458452	AAATATTCTGACTCC[A/G]AGGTCCTGCCTCCCA	55764
rs530293190	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509793	CTCCTTTTAGAGAAA[A/G]CAGGCTAGTATGTTG	55764
rs530373799	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444377	TCATCCTTGTTCCAG[C/G]TTCTTTATCAGCCAG	55764
rs530376966	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481175	TGTTCATAGTAGCTT[C/T]TTCCTGTGTTAGTTC	55764
rs530432109	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485892	GTCGCCTCTGCCTCC[A/G]GCCATCCTGTGGTTT	55764
rs530442339	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129474002	CCTTCCATGTCGTGA[A/T]TCATAAGAATTTTTA	55764
rs530473974	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506999	GAAGGAGTAGTGGAA[A/G]TGGAAGAGACAAGGA	55764
rs530478134	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129517870	TAAAAGGCACTGGCT[A/G]TGCCTCTGTCTGTGC	55764
rs530496565	snp	A/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129515843	CCTGGCGCAGGGCTT[A/T]ACATAACCAAATGCC	55764
rs530545556	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129491933	TGGGATGTCTTTGCT[A/G]TTCTTTACATGGTCC	55764
rs530560473	snp	A/G	0.0399052	0.1355	intron-variant	IFT122	GRCh38.p7	3:129516698	AGATTGCTCCTGCAC[A/G]CACACACACACACAC	55764
rs530572589	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510479	CCCCTCAGGGTCCCT[C/T]ATCTTTATCAGGTGC	55764
rs530589515	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519922	CTTCACTGGCCCCTG[C/T]GCTGTCCACATCCTC	55764
rs530608819	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467983	AAATCACTGATCCAT[C/T]TCACAGGGACTGAGC	55764
rs530620979	snp	A/G	2.41211e-05	0.00347275	intron-variant	IFT122	GRCh38.p7	3:129461017	CAAAAGTGAGTCCCC[A/G]TCTCTACAAATAAGA	55764
rs530654242	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504519	CTTCCCATCTGTAGA[C/T]CCCAAGATAGATGAC	55764
rs530655085	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474721	AGAGAATGACCTTGG[G/T]GGCTGAGCTCGGGAG	55764
rs530681243	snp	G/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129453865	AAGAAATGGGCTTTG[G/T]AATGAGACAGTTGTG	55764
rs530715397	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493508	CCTATTCCATGCAGG[A/G]GGAAATTAAGGCTCA	55764
rs530722672	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129460143	AATACATTTACATTG[C/T]TGTGCAACCAATCTC	55764
rs530774287	in-del	-/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129492312	AGCTCACTGGCGTCT[-/G]GGCATCTGGGCCACA	55764
rs530872444	snp	A/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129459137	ACTCAAATGTCAGTT[A/T]CTTTGTAAGGACTTT	55764
rs530907002	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129503055	CTGAGCCACAGAATC[A/G]TGGAGGGCCTTTCCA	55764
rs530910587	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497947	GTGACATGTTTATAT[A/G]GTGATAAAGGGAATT	55764
rs530917892	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465540	CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC	55764
rs530936539	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458514	CTTACTAGGTACCTT[A/G]AAGAACTAGTTTTCT	55764
rs531006707	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444553	TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCAGGC	55764
rs531010382	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452326	ACAGTAAACATAGTA[A/C]AAAGGTAAATTAAGT	55764
rs531015578	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129497568	CCCTGCTCTGAGGCC[C/T]CTCCTTACACTGTGG	55764
rs531030089	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491720	GCTGTCCCCTGCATT[C/T]TACCCATGTTGCCAA	55764
rs531047409	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445178	CAAAAATACAAAAAT[G/T]ACCTGGGTGTGGTGG	55764
rs531082290	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438604	AATACTTCTCCCCCA[C/T]ACTGTTATTGAAAAA	55764
rs531091599	snp	C/T	0.00271446	0.0367405	intron-variant	IFT122	GRCh38.p7	3:129492133	TATTCTTTATTTCTT[C/T]GCCACAGGCCTTCAT	55764
rs531110206	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441261	TCTTTGGTTCTGTCC[C/G]TTCTGAGATCTTTCT	55764
rs531175551	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496899	TTTAACTCAGGATGA[A/C]CCCTTAAGGGATCAA	55764
rs531211047	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486693	GATGGTGAGGAGCTG[A/G]TGCTGAGAAAATACA	55764
rs531281244	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484346	CAGAGACGTGCATAG[C/G]GAGAAACTGTAGCCT	55764
rs531286206	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490685	AGCGAGGACTCAGAC[C/G]TCGAATGCTCCTTTC	55764
rs531333075	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450212	AAAACAATCACAATG[C/G]CTTTGAAACTGGACT	55764
rs531342316	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129447417	TGGGATCAACAGAAA[C/G]GAATGTCTGGGTTAA	55764
rs531345983	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129450808	TTACTGCAAGCTCCA[C/T]CTCCCGGGTTCACAC	55764
rs531361187	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485607	ACCAGGAACTCATCT[C/G]CCTCAATTGCCCCAA	55764
rs531387948	snp	A/G	1.86204e-05	0.00305121	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520176	GCTGTCTTCCCTTAG[A/G]TGTTCCATTCTGAGG	55764
rs531450827	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129514777	ACAGCCCCCGGCCCC[A/G]GCCTCAGCCCTCAGC	55764
rs531454251	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	IFT122	GRCh38.p7	3:129520780	TGGGGGAGCAGGGGG[G/T]TTTTTTGTTTATTTA	55764
rs531462780	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129515209	GCTAATGGTGGCAGC[A/G]GCCACTGTCATTCCT	55764
rs531468624	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508118	ATTAACCAAAGGCTC[A/G]AGATCCCTCCCTGGC	55764
rs531477292	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484941	ATCTCCCACCACAGT[C/T]ATGGCACTGAACACT	55764
rs531485186	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478808	GATATACTTTAATGA[C/T]TTAAAACATAAATTG	55764
rs531493309	snp	A/G	0.00557542	0.0525036	intron-variant	IFT122	GRCh38.p7	3:129497648	CACTCCATTTGCTCC[A/G]TCTCTCTATGAAGGT	55764
rs531547637	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129494891	AGGGTCACTGAGAGG[A/G]ATAAAGGGGCCATGT	55764
rs531582623	snp	A/C	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129462843	CAAGCCTTAGGTGAC[A/C]AGTGTGCCATGGGAG	55764
rs531588183	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441901	GAACATTTGGCTTCA[A/G]TGTCAGAGTAATAGA	55764
rs531612042	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477348	TCCACTTAAGTTGCT[C/G]TGCTGGTTAAATAGA	55764
rs531621998	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129480160	AGCTATAACCTTTGG[C/T]TACATGTAGAGTGTA	55764
rs531664036	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129472300	CTGGGACTACAGGCA[C/T]ATGCCACCACATCCT	55764
rs531664463	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129464856	CTTCCTGAGGTCTCC[C/G]TACATTCAAAGGCTT	55764
rs531783850	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477646	TTACATGTCTTCCCC[A/G]TTTGTCAAGGAGGTG	55764
rs531799197	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513687	TGAGGAGTCATGCTG[C/G]AGACACAGAAGGAAA	55764
rs531884692	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496454	GTCAAAAGTGGCTCT[C/T]AGTATGTTATGAAGT	55764
rs531995493	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457078	TAAAGTCTAAAAGTC[C/G]TTAAGATGTACAGAA	55764
rs532022508	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501530	GTTCCCCACATTATT[A/C]TTTAAATGAAGGGGT	55764
rs532109191	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129510438	CTCATCTTCCCTTAC[A/G]GTCTTTGGCTTTCCT	55764
rs532134140	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480345	GCTGGGTCCTCAAGA[C/T]ACTGATAGATGTCAT	55764
rs532193037	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473982	CCATTTCCAGAAGCT[A/G]CTAGCCTTCCATGTC	55764
rs532216598	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509290	AAATGCCAAACAACC[A/G]TAGAATGGTTGACAT	55764
rs532228804	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509900	TCTCTATAAAATAGG[A/G]ATAACAGCACTATGT	55764
rs532280901	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479620	GGGAAGCCTTGCATG[A/G]AGTCTTGGATTAACG	55764
rs532291502	snp	A/T	0.00676609	0.0577691	intron-variant	IFT122	GRCh38.p7	3:129472334	AATTAAAAAAAAAAA[A/T]TTTTTTTTTTTGGTA	55764
rs532482212	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466247	TACTTGATTTAGAAG[A/G]TTGTTTGGAAGGTTA	55764
rs532491363	snp	C/T	0.000181433	0.00952279	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478095	ACTGCCAGAGAAAAT[C/T]CTCATCTATGAGTTG	55764
rs532499939	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464221	CCCTTCCGTTCAGCA[C/T]CTGTTGAGCACCTTC	55764
rs532514926	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129519383	GACCATGGCCAAGGG[C/T]GCAGGTCTGTGGACA	55764
rs532526957	snp	A/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129471160	GAAGCCTTTAATTGC[A/G]TAGCATCCTTATTCC	55764
rs532555588	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470732	TGTGCCACCATGTCC[A/G]GCTAATTTTGTATTT	55764
rs532559203	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457137	GTCTCTCACCAGAGT[A/G]GGTGAAGACCCCGTT	55764
rs532573188	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457656	TCAGACAAAAGGAGT[A/G]CATTTTTGAGATCTA	55764
rs532583426	snp	C/T	1.64893e-05	0.0028713	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458677	GCATTCTGAAGTACA[C/T]GTAAGTAACTTAGGT	55764
rs532603108	snp	A/G	0.000149233	0.00863679	intron-variant	IFT122	GRCh38.p7	3:129514566	TGAGGTGAGGATGCA[A/G]CACCCTTGGGCAGGT	55764
rs532707536	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129497390	TTCCCTTCTCAGATG[C/G]TAATAGCGACAGCTC	55764
rs532755439	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129488684	CAGGAGCAGCATGTC[A/G]GATTCTGGCTGTCAC	55764
rs532790656	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506266	TTAGAGAAGCGCCAT[A/C]CCAGCAACGAAGCAC	55764
rs532793692	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129455483	GCCCAAGTTTAATAA[A/G]TATTTAATGAGCAAC	55764
rs532838860	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129496982	GCAGCTGTGCTGCAG[C/T]AGAAAATGCCTGACC	55764
rs532848074	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129448731	GAGTCTTCCTCCGTC[A/G]CCCAGACTGGAGTGC	55764
rs532885836	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129495193	ACACAGGAAAGCAAC[A/C]CTGAGGAATTTCCAT	55764
rs532910154	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503894	GAGAAGCAGTCAGTG[A/G]GTCCATACAGCACGA	55764
rs532927169	in-del	-/CTC			intron-variant	IFT122	GRCh38.p7	3:129492031	GCTTGCTCCCTTCCT[-/CTC]CTCTGTGGCTCACTG	55764
rs532948066	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462488	AGTGGAGGAACCAGG[G/T]CTTGGACTTTAGACC	55764
rs532957628	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468455	TTCTAAGCGATTCTT[A/G]TGCCTCAGCCTCTGG	55764
rs532959630	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509017	GCAGACCACCAAACA[A/G]TGATCATGACCTTTT	55764
rs532962259	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129462972	CTCTGGTTGCAGTGT[C/T]AAAGTTATAAACAAT	55764
rs532993714	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441969	GGGCAGCTGCTGCTC[A/T]GCTCCTGCCAATTAC	55764
rs533030782	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129442585	AAAACTAAACAAAAA[A/C]AAAAAAGACAGTAGA	55764
rs533042342	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518881	TGCTTCCCACTGGCC[A/C]TGGGAGCTATGGTGT	55764
rs533059616	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129495782	CCACTGGTTGAAACT[C/T]ACCTAAAACTGACCT	55764
rs533088112	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464550	CATCAGACTTTTATT[G/T]CAAACCAAGGCATCA	55764
rs533115634	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129454135	CCACTTTCTAGAAAG[A/T]TGCAAATTCTTCATG	55764
rs533121497	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487851	TGAGACTCTTTCCCC[G/T]GGGGTGGGGGCTTGA	55764
rs533133032	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489392	AGTCATGAGGCTTAA[A/C]TGAGATGTTGTAAAG	55764
rs533147219	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449342	ATAAGACACAACCTT[A/C]GAGGTGAGAAAATGT	55764
rs533170603	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447040	GCTCTAGCCCATTTT[C/T]CTAGCCTCATTTCTC	55764
rs533239137	in-del	-/TTG	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129473922	TTGGTCCAGAGTTTA[-/TTG]TTGTTACTTTGTGGG	55764
rs533241352	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489895	TCTCTATGGAGGGAG[C/G]TTCCCTCTCCTGCCC	55764
rs533241476	snp	A/G	4.00136e-05	0.00447272	missense	IFT122	GRCh38.p7	3:129483617	CAGGGCTTTGTGGTC[A/G]GCTACAATGGCTCCA	55764
rs533304167	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482430	CCCCCAAAGCTGGAG[A/C]CCCTCCTGACTGGTT	55764
rs533305600	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129484092	GGAGAGAGAGAATGA[C/G]TGGGTGGGGGGTGTG	55764
rs533318557	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475758	GTTGAAGGCTGCAGT[A/G]AGCCGTAATTGCACC	55764
rs533339040	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517867	CCCTAAAAGGCACTG[A/G]CTGTGCCTCTGTCTG	55764
rs533400682	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440407	CGAAGAGCAGGAGGT[C/T]GAGTCCTCGCGGGGA	55764
rs533437816	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440690	CTGCTCAAGCTTCAC[A/G]GTTCTTGCCACATCC	55764
rs533531450	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440973	CGTTTCTCTAAAACT[C/G]GAGATGGGCAGGTAT	55764
rs533585523	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468549	GGGTTTCCCCATGTT[C/G]GCCAGGCTGGTCTAG	55764
rs533591222	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476565	GCACTGAGCAGCCGC[C/T]GTGTCTCGAGTCACA	55764
rs533697759	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468896	TTAATTTTCTTTCTT[C/T]AGGAAGAGCAAGCAA	55764
rs533719732	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129518915	TGGCCTGCGAGGGGA[A/G]TGGGTGAGGGCAGCA	55764
rs533721153	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469253	AACCTGAGGCCAGGA[C/T]TTCCTTGTTCCTGTT	55764
rs533730915	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513295	CCTGTTCTTTTCTAA[A/G]TCTCACTGTACTCTC	55764
rs533756705	in-del	-/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129454662	GCTGTTGAGGAATGT[-/G]GGGTCAGTCCAGGGC	55764
rs533800174	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441375	TTTTGTGTTCGGCAC[G/T]AGTGGTAGCTGACAC	55764
rs533817664	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488929	GGATTCATGGACTTG[A/C]TTCGTTGTGTCCTTT	55764
rs533868914	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483257	TCAAAAGTAATACTT[C/G]CTTACTCAAAAATTC	55764
rs533882069	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483748	AGGGAAGCTGGGCCC[G/T]TTGCTGGTGCTTTGG	55764
rs533885295	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471638	CCCAAAGTTTCTGCA[C/T]GATGAGCAACCTTAA	55764
rs533948736	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477624	AGAGCCTGGTGTGTA[C/T]CAGAAATTACATGTC	55764
rs533987570	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504809	AAAGAGGTGAAGAAA[C/T]TTGCCTGAAGTTTCA	55764
rs534022519	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468202	CTTGGCTGGGTTTTA[A/C]AAACAAGGCTTTACC	55764
rs534076018	in-del	-/TT	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129452553	GGGGGAAGAGAGCTC[-/TT]TGCAGAGGAAGAGCC	55764
rs534079230	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470136	AGGCAGGAAGGAATG[A/G]AAATATATGACAGTT	55764
rs534154342	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475459	GAGTTTGAGACTAGC[C/T]GGGACAACAAGGAGA	55764
rs534189142	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129502892	GATGAGGTGAGGGGA[A/G]AGCAGGCCTCATGGG	55764
rs534217887	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494598	GGCTCAGGGTTTGGG[C/T]GCTACTGAGTGTTTA	55764
rs534229449	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488596	TTGCTTCTCTATAGA[C/T]GTAGGATGATGACAG	55764
rs534244228	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517921	ATGGGACATGATGTC[A/G]TGATGTCGGTGTTGG	55764
rs534278044	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459459	CATGCCAGGCTAATT[C/T]TTTGTATTTTTAGTA	55764
rs534322065	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452816	AGGTGAGGGTTAGGA[C/T]ATCTGTGTGAGGAAG	55764
rs534324933	in-del	-/CCCTGTTGGAGCC	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129505380	GCAGAACAAATGTCT[-/CCCTGTTGGAGCC]CCTCAACCGAAAGCC	55764
rs534337287	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461322	ACGTTCTGATTCCTG[A/G]TGTCCTGTCCTGGAA	55764
rs534341675	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456720	AGGAGTTTGAGACCA[G/T]CCTGCCCAACATGGA	55764
rs534349736	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461976	CTATCAGTCTGTGTT[C/T]GTTGCTAGTGGATAC	55764
rs534396077	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129517686	CAGTCCCAGGGGATC[A/G]CGGGCCATGCTGAGC	55764
rs534475147	snp	A/C			downstream-variant-500B	IFT122	GRCh38.p7	3:129520668	TATTGTCTGCAACTT[A/C]ATTTCCGTATGCAAA	55764
rs534478560	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510858	GACACGGTGGTGAAC[A/G]AAACGTTGTCCCTGC	55764
rs534497752	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446544	AGATAAGCTCAACCA[A/G]TTGTCAGAAAAATTT	55764
rs534527151	snp	C/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129495349	TCCAGTAGGAAGGCC[C/G]AGGGGCCTCACTTGA	55764
rs534533583	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439890	GCCCAGGGTGTGGGG[C/G]GGAGTAAGATGTGAA	55764
rs534567294	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467257	AGTGATCCTGTGAGA[A/C]ACTATAGGAAATACT	55764
rs534581151	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129503455	CTCAGGCTGGCAGAA[A/G]CAGCTGATGCTGCCC	55764
rs534597672	snp	A/G	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129487874	GGGCTTGAGGGGCTT[A/G]GGAGGACTCTGCAGA	55764
rs534611185	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481974	TCTTAAGCGTTTACC[A/G]TGAACAAGAAATGGG	55764
rs534648345	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129504070	ATTCTGTGCCGCTTC[C/T]GTGGTCCAGAAACAG	55764
rs534658202	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498335	GATGCCTGTTTTCCT[C/G]CAGCTGCCACCCTCA	55764
rs534726239	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129444647	CTGCCTCAGCCTCCC[G/T]AGTAGGTGGGACTAC	55764
rs534740206	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129491794	CCTGCTGTGATGCTG[C/T]GTGACCCCCCAGAGG	55764
rs534755342	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129510847	TGAGACCTGGTGACA[C/T]GGTGGTGAACAAAAC	55764
rs534759841	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129482166	AAGGGGATGGGCAAG[C/G]CTGGCCTTCTACTTA	55764
rs534835449	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447100	AGATGTTTCAGTCAA[A/G]TTAAATTATTTTGAT	55764
rs534874339	snp	C/G	0.33875	0.233717	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440426	TCCTCGCGGGGAGTG[C/G]GCGAGCCGCTGCAGC	55764
rs534899658	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129466063	ATCCACCCACCTCAG[A/C]CTCCCAAAGTGCTGA	55764
rs534910551	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515894	CTTTGCATTCAGACC[A/G]GGAGGCTGAGATAGG	55764
rs534989271	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473592	CTCTGTGCAGTTCTT[C/T]AGCTGTAGCTAGGCT	55764
rs534999453	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444144	TCTATCCTTGTTTTG[C/T]AGGTGAGAATGAAAG	55764
rs535052561	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466752	GAGCGATTCACTTGC[C/G]TCGGCCTCCTGAAGT	55764
rs535082623	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129454262	GGCTCATGCCTATAA[C/T]CCTACTGAAATCCTA	55764
rs535106683	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446602	CTGCTTCAAGTTGTT[C/T]CATCTTTCTGGACCA	55764
rs535133689	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486813	CAGGACATCTAAACA[A/G]AAGTTAATGGATTTA	55764
rs535203017	snp	C/T	3.59318e-05	0.00423847	intron-variant	IFT122	GRCh38.p7	3:129515455	GGACACGTGCCTGCC[C/T]CGGCCCCTCGGGAGT	55764
rs535263775	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482064	TCCTTTGCAGAAGTC[A/T]GTGTCTCACCTGCTG	55764
rs535270845	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440450	CTGCAGCGTGTTTGA[A/G]GGGGGCAGCGGGCTT	55764
rs535311841	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440475	GGGCTTGCTGCCTGG[A/G]CCGAGGGCACTGAAC	55764
rs535340469	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475419	CACTTTGGGAGGCCA[A/C]GGTGGGTGGATCATC	55764
rs535405151	snp	A/C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490470	TGAGCTCATTCAGGG[A/C/G]CCTTGTGACTCTGAC	55764
rs535411469	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129494531	GATTCAATGTCTTAT[C/T]GTCCTCCAATATGCT	55764
rs535449504	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486891	TAGGTCACCTGCTCC[A/G]TAGCCTATGCCTGCT	55764
rs535497644	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438865	CTTAAGTCCGGCAGG[G/T]CAAGGCTTCAGGGAG	55764
rs535532682	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493631	CATACCCTCCCTACC[C/T]GCGTGTTGTAAGGGG	55764
rs535569966	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442061	TCTGGGTTTTTATGT[A/G]AAATGGCCTAATTTT	55764
rs535606113	snp	A/G	9.89854e-05	0.00703441	synonymous-codon	IFT122	GRCh38.p7	3:129488397	TGAAACAGCAAAGAA[A/G]GTAAGCATCTAGCCA	55764
rs535652251	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440865	CAGCGTCGCTTGCTC[C/T]AAGTGTAAAAGTAAA	55764
rs535657700	snp	A/G	3.29527e-05	0.00405898	missense	IFT122	GRCh38.p7	3:129517510	CTGGAGGAAGGGATC[A/G]CTGATGAAGAAGCCA	55764
rs535660313	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129465703	TGCGGACTGCAGTGG[C/T]GCAATCTCGGCTCAC	55764
rs535685597	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467378	TCTTTTCGTGTGTTC[A/G]TATAATTAACTAAGT	55764
rs535719121	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517961	CTTCCACTCAAGTCA[C/T]TTTCGCATGCAAGTG	55764
rs535734488	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504165	CTGATTTGTTTTTGC[A/T]TTTCTGTGGGTAGTT	55764
rs535830785	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129503378	CCACCCCACAACCAC[A/T]ACTTCTCTCTGGTGT	55764
rs535838151	snp	G/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129470618	CTCTGTCGCCTAGGC[G/T]GGAGTGTAATGGCTC	55764
rs535897421	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502435	TGGGTACCTGGTAGG[A/G]GATTAGGAGATAATT	55764
rs535928565	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472498	GAAAGATAAGAATTA[C/T]ATTTAAAGTGTATAT	55764
rs535962927	snp	A/G	4.94474e-05	0.00497205	synonymous-codon	IFT122	GRCh38.p7	3:129502789	CTACCTCAAGAAGCT[A/G]GACAGCCCTGGCTAT	55764
rs535995066	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481404	GAGTCCTTTTCCCTG[C/T]ACAGAGCTTCTGGTG	55764
rs536001322	snp	C/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129470294	TTCGAGATGGAGTCT[C/T]ACTCTGTGGCCCAGG	55764
rs536031888	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510254	TTGACCTCTCAAATG[C/T]CCTGCCTTCCACCTT	55764
rs536070913	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497732	GTTGGTTCCTTTTCA[A/G]TCCCCCCTGCCCCCA	55764
rs536133756	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129498096	TTGCCATGGCCCCAG[A/G]TAATGTGTAACTTAG	55764
rs536157886	snp	A/C	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129448587	AAATTAAAGGGAGGA[A/C]AGAACCTCCATGTTG	55764
rs536172097	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498784	ACAAAGTACTCTCCA[C/T]AGGGTACATTATTCC	55764
rs536206280	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456828	GGCTGAGGCAGGATA[A/G]TCGCTTGAACCCGGG	55764
rs536213125	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464255	AAAGCAAGCACTGTT[C/G]TAGGGGTTGGAAGAC	55764
rs536292111	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508621	AACCATTATGATCAA[C/T]ACATTTTTGCCAATG	55764
rs536332543	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129465187	GATGCAGCAGGACCA[C/T]TTCCTTATGAATCAA	55764
rs536396489	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458003	TCAGCCCTCCAAAGT[A/G]CTGGGATTACAGGTG	55764
rs536451700	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129451740	GGGTCCTCTACTTCT[A/T]GGTTACCCAACTTTA	55764
rs536460612	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129443785	AGATTGGGGCAAATC[A/G]GACATATATGATATA	55764
rs536523380	in-del	-/AG	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129488030	GAGGGGAGGATGGGC[-/AG]AGAGTTTGTGCTGTG	55764
rs536525570	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478404	CTCTATCAGCAAGTC[A/G]TGAGCCATAAACTGG	55764
rs536587757	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129444718	GTAGAGATACAGTTT[C/T]ACCATGTTGGCCAGG	55764
rs536589600	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452551	CGGGGGGAAGAGAGC[C/T]CTTTGCAGAGGAAGA	55764
rs536602047	snp	C/T	0.220246	0.248223	intron-variant	IFT122	GRCh38.p7	3:129465803	GCCCGCCACCGCGCC[C/T]GGCTAATTTTTTGTA	55764
rs536676038	snp	C/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129496011	CCGATCATGCAGGAC[C/G]ACATGGTGCCTGCCA	55764
rs536698951	snp	A/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129503372	CTGCCCCCACCCCAC[A/T]ACCACTACTTCTCTC	55764
rs536737182	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496561	CCCACTTTTTTCTGC[C/T]TTTCTATTCCTGAAG	55764
rs536754083	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490365	GAGATGGACAGCCAT[C/T]CCCACTAGATGGCAG	55764
rs536772001	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498204	GTCACAGCTCCCTGA[A/G]TGACCAGCTGGCCTA	55764
rs536774431	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459414	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	55764
rs536848093	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519916	AGTGGACTTCACTGG[C/T]CCCTGCGCTGTCCAC	55764
rs536919008	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129511819	AGAGGCATGTGGGTT[C/T]ATGCTGGAGAGGGCT	55764
rs536919948	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520386	AAGTTTGTGTTTTGT[C/G]GGGGGGGCCTTGTGT	55764
rs536936823	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492822	TTTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTCTG	55764
rs537066272	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129458947	GACTTTATCCCACCC[C/G]CAACCTGTCATCTTC	55764
rs537108298	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443919	GTGATAATTCAACCC[A/G]AAATGACCCTTATGA	55764
rs537111041	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497777	TTTGAGAAATATGTA[C/G]CTACACATTATGTGG	55764
rs537144081	in-del	-/CCT	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129505108	CTCTCTGTGTCAGGC[-/CCT]GGCTGAGCACTTAAC	55764
rs537151729	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518761	TCGCCCCTGTCTGCT[C/T]CATCACAAGTGCCCG	55764
rs537211314	snp	C/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129485923	TGGCCCAGAGAGGAG[C/G]GAGAAAGCATCAGAC	55764
rs537235340	snp	A/G	3.3117e-05	0.00406908	missense	IFT122	GRCh38.p7	3:129514546	GCCAAGCCCTTCCAC[A/G]ACAGTGAGGTGAGGA	55764
rs537253672	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453191	CTAGGGCATAGACGG[A/G]GTATTTGCTTTAGAT	55764
rs537302972	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129446419	ACGGGGTTTCACCGT[C/G]TTAGCCAGGATGGTC	55764
rs537324988	snp	C/T	0.000148418	0.00861319	intron-variant	IFT122	GRCh38.p7	3:129479745	GTCTGGGGGCACTTA[C/T]TCTGTTGAATTTCCA	55764
rs537327547	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471918	CTCTTTACAAGGATT[A/C]ACTCTTTTAATCCTT	55764
rs537391221	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472721	CACTTACATTAGACC[C/T]TTTGTTACTGTTCTC	55764
rs537430793	snp	C/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129492979	TGTGCCACCCCGCCT[C/G]ATTAATTTTTTGTAT	55764
rs537453627	in-del	-/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129476606	TTGTGTCTGACAAAT[-/G]GGGGAATGCAGACTT	55764
rs537468030	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497151	GCTGGTGCCTGTAGT[C/G]CCAGCTACTGGGAGG	55764
rs537470029	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490468	GCTGAGCTCATTCAG[A/G]GGCCTTGTGACTCTG	55764
rs537610918	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129443059	TTCATGCCAGCTAGT[A/G]TTTACTGAGTACTTG	55764
rs537705450	snp	G/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129515435	GCCAGAGTCCAGGGG[G/T]AGGAGGACACGTGCC	55764
rs537786234	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465864	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT	55764
rs537798440	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129468628	GAATTACAAGCGTGA[G/T]CCATCACGGGCTGCC	55764
rs537838642	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512597	GGCCCAGGGGCCCAG[A/G]CCAAGAGAAGATGAG	55764
rs537899725	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499819	AGCCATGTGGAGCCC[A/G]CCCTTGCTGCTAGAA	55764
rs537927492	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129477695	GTGAGGTCAGTTACT[C/T]AGGCAGGCTTCTGAT	55764
rs537981794	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455298	CTGCCTCAGCCTCCT[G/T]AGTAGCTGGGACTAC	55764
rs537982183	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470286	TAATTTTTTTCGAGA[C/T]GGAGTCTCACTCTGT	55764
rs537990496	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471016	TTCCATGGAGGGTGG[A/G]TTAAAATATAGAGAG	55764
rs538009563	in-del	-/T	0.00557765	0.0525139	intron-variant	IFT122	GRCh38.p7	3:129451100	CATATTACAGCTGGG[-/T]TTTATTTTATTTCTT	55764
rs538053204	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129464399	TACAGAGGGCTGGGG[A/G]AGCTCAGAAAAAGGC	55764
rs538076417	snp	C/T	3.47808e-05	0.00417003	intron-variant	IFT122	GRCh38.p7	3:129495395	CCTTTGTAAAGGCTG[C/T]TTCCTGCCCATGGCT	55764
rs538093595	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507336	CCTTTGTCCCAGCAG[C/G]CTCTTCCGACACATC	55764
rs538140101	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129495956	CAATCCTTGTCAGGA[A/G]CCGCCAAGAATCGGT	55764
rs538145570	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489060	CTAGAACCTCAGATG[A/G]AGGAAGGAATGGCTT	55764
rs538150414	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489605	AGCACTTTGGGAGGC[C/T]GAGGTGTGCGGATCA	55764
rs538151438	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129496662	CAGGACCTATTGTTC[A/G]TCAGGACTTGGACGA	55764
rs538157554	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129483282	AAATTCCAACAACAC[A/G]CAGGTGCATGGAGGG	55764
rs538167926	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457345	TCCCATTGCTTTAGG[A/G]TAAAGAGCAAGGCCT	55764
rs538179022	snp	A/G	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129512746	GGCTTGGAACCTTGG[A/G]CACTTCTCCAGACTG	55764
rs538193364	snp	A/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439019	AAAATTAAAAAAAAA[A/T]TTTCAGTAAAGTGTA	55764
rs538233533	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481883	ACACAGGCACAAGCC[A/G]CAGGGCCTGGACCGG	55764
rs538261750	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520362	CAGAATGTGTTTCTT[A/G]CCCAGATGAAGTTTG	55764
rs538291650	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513162	TGTAGCCATCGAGGG[C/G]CACAGTGGTACCATA	55764
rs538293401	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450303	TCCATGAAAAGTCAG[A/G]TAGCCTGACCCCAAC	55764
rs538299047	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506026	TCCAAGTGCAGTAAA[A/G]TGGCAGGTCCTGTTT	55764
rs538314439	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507455	GGCCTTATGCCCTGT[C/T]CACCTAAGAATTCAC	55764
rs538321164	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514819	TGCTCCTTGCCCTCC[C/G]CTAGGCAAGCCCCAC	55764
rs538339242	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478955	TTCTCAAGATTCTTA[A/G]AGAGTGTCTAAGTCA	55764
rs538364398	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129462645	ATGTTTGGAGGAAGC[A/G]TTCTGGACCAGGGGA	55764
rs538465182	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448879	AATTTTTGTATTTTT[G/T]GTAGAGACAAGGTTT	55764
rs538466268	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129480838	TGTCAAAAACAGATA[C/T]CATCAGGGTTGGGAG	55764
rs538491759	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129502394	AAGATTCTGATTTCA[C/T]GCATGGGAAAGCTCA	55764
rs538503357	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441487	TCCTCTATTTTATGT[A/G]TGAGGAAACTGAAGC	55764
rs538605599	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462697	GATGTTGCACTTGGC[C/G]ATGTATTTGTGCACT	55764
rs538619105	snp	A/G	9.909e-05	0.00703812	missense	IFT122	GRCh38.p7	3:129519706	CTGCCTGACGCCTCC[A/G]TTACCATGTGCCCCT	55764
rs538635135	snp	C/G/T	0.000297513	0.0121931	missense, synonymous-codon	IFT122	GRCh38.p7	3:129514452	CAGGCTGGCCCGGCA[C/G/T]GCCTATGACAAGCTG	55764
rs538665210	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129463437	TTGAGATTATGTTTT[C/T]TCATTCAGCATAAAA	55764
rs538676584	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129455922	GGAGGAGGAGGAGGA[A/G]GAGGAAGAGGGATTG	55764
rs538703555	snp	A/C	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129500498	GCTTTAGCCTCTGAT[A/C]TGCTGGATGTCGATG	55764
rs538778824	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456690	AGCACTTTGGAAGGC[A/G]GATCACCTGAGGTCA	55764
rs538942650	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491268	GTCAGGATTGCTCTG[C/T]GTGTTCAGTTCAAAG	55764
rs538946119	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490166	CCACACCCAGCCAGA[C/T]TTACTATAGTTGAAA	55764
rs538946237	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483939	AGGGATGGGAGGGGT[A/G]TGCAGTGTTGTCAGC	55764
rs539011145	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129513808	GCCTGGGGGCAGCCA[A/G]CATCGGAGGTGACCT	55764
rs539013157	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506091	AATGAGCAGGGGGCA[A/G]AACCTCACTGAAGAT	55764
rs539014101	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129460535	AAACTGCTGGGATTA[-/C]AGGTGTGAGCCACTG	55764
rs539045246	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447525	TAAAATGTTTCTTCT[C/T]ACCCTGCAAAACAGA	55764
rs539083260	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501094	GAGGAGGGGGTTGGG[G/T]TGGGGCAGCACTGAG	55764
rs539099713	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129512127	AATGCATACCACAAG[G/T]TTATTATGTTAAAGA	55764
rs539105138	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440922	AACAAGCTGTAGCTA[C/G]CTATTGTTGCTAGGG	55764
rs539204554	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449617	CAGTTGACCCTTTGA[A/C]TAATTTCTTGTGTCT	55764
rs539228134	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476154	GATGCAGAGGCAGAG[A/G]GGCCTGTGTTCACCA	55764
rs539246060	in-del	-/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129496551	GAAAATCTTCCCCAC[-/T]TTTTTCTGCTTTTCT	55764
rs539352529	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129514895	AGAGCTGACTCTTAC[C/T]CTAGAAACCTCTGCC	55764
rs539454968	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441770	TCTTGAAACACAGCC[A/G]TATCAGTGAATCTTT	55764
rs539528474	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474378	ATGTTAATCACAAAT[A/C]GTCTTTTTATTCACA	55764
rs539536928	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488496	AGGCCATAGACTGCA[A/G]CAGTCTCTGGAGTTA	55764
rs539549798	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488893	CAGCAATGTGGGCAC[C/T]TCCCACGTACCTTCA	55764
rs539562123	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129462545	GCTAAGCACTGCTGA[A/G]GGAGGCCCAGGAGGA	55764
rs539568950	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129469073	GAGGTTTATCTTCTT[C/T]AGCTGCAGCAGTGTC	55764
rs539598996	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445492	AGGTTAACATGAGTT[A/G]ATACATGTAAAGCAT	55764
rs539625157	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518610	CCACTCCAACTTGGT[A/G]CCAGCAGTCCCCATG	55764
rs539684530	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504738	CCTCGCAACAGCCCT[A/G]TGGTATAGCTACCAT	55764
rs539695764	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505079	ATTAATCATATTTTT[A/T]AAAGTTGACTTCCCT	55764
rs539705079	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499206	ACAGGATCCCTAACC[A/G]TTCAGCTGAGAAGCA	55764
rs539711427	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513256	AGATTTTTAAGGTCT[C/T]GGATGTCAGGAGACA	55764
rs539775738	snp	A/G	0.117537	0.212022	intron-variant	IFT122	GRCh38.p7	3:129454509	TGTACCATGGTAGTC[A/G]TATTTGTGTGTGTGT	55764
rs539802021	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469782	CTTTCCTCTATTCGC[C/T]TTCTTTCATTCAACC	55764
rs539825456	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129498555	TTGGGTCCCAGCATC[A/C]GGGTATACAATGCGC	55764
rs539846883	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129517710	GCTGAGCCTGGCCCT[C/G]TGTTCCCAGAGAGAT	55764
rs539851635	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445762	TCCTCATCTACAAAA[C/T]AGAGTAATAATTCCT	55764
rs539884465	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517337	CATACAGAGACTGCC[C/T]CTGCTGCCTCTTCTT	55764
rs539899842	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129481933	CTTGCCAATGGAAAC[C/T]GAAGGCTCTGAGCCA	55764
rs539927668	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129468494	GGATTACAGACACGC[A/G]ACACCACGCCGAACT	55764
rs539955704	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487670	GAGGCCATTCCAGAC[C/T]GCTTCCTCCCACGAA	55764
rs539964451	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475164	ACATTTCTCTGTGGC[C/G]AATAAGCACATGAAA	55764
rs539993382	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129468150	TCTTTGTCTCTTTTC[C/T]CTTAGTTTTGGGTTA	55764
rs540001181	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504254	AATGGATTCAGCCAA[A/G]TACAGTGTTTTCATG	55764
rs540109127	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494947	TAGTGGATGTTCAGC[A/C]TGCGGGATTTCTTAC	55764
rs540143354	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462825	ATCTGGGACAGGGGG[A/G]AGCAAGCCTTAGGTG	55764
rs540150745	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499698	TGTCCCAGGATCCCC[C/T]AGGAACACCTGCAGG	55764
rs540158680	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493882	CTCTCCTCGTATGCT[A/G]TGAGCTGGGAAGTGC	55764
rs540184341	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456039	TCAACTGTATGTACA[C/T]ATGTACATACACTCA	55764
rs540200599	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475661	TTTTTCAAAAAAAAA[A/T]TTTTTTGCCAGGCAT	55764
rs540289492	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457016	GAAGGCATTGAGGCT[C/T]AGAGAACAGTGACTT	55764
rs540334278	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468730	TGGTCCTACAGTCCC[A/G]GCCCCACAGCACTGA	55764
rs540474261	snp	C/T	4.94189e-05	0.00497062	synonymous-codon	IFT122	GRCh38.p7	3:129499994	GGAGCCCAAAGCCGC[C/T]GTGGAGATGTACATC	55764
rs540498688	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487708	ATTGTGTCAGCAAAC[A/G]TAGACTGGGGTTCTG	55764
rs540514895	in-del	-/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129498328	CTCCTAAGATGCCTG[-/T]TTTCCTCCAGCTGCC	55764
rs540589538	snp	C/G	0.000399281	0.0141238	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451957	TTCAGCCCCTCAAGG[C/G]ACACAAAGACACTGT	55764
rs540596931	snp	C/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129467818	TTTCCTTGGAAGAAT[C/G]CCACCCTGAGGTCAT	55764
rs540606799	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129460005	TGGGCTCAAGCAGTC[C/T]TCTCAAAGTACTGGG	55764
rs540675120	snp	C/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129444934	AATTCTTCATGTAAT[C/G]CCTTAAGTAGGTAAT	55764
rs540684336	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486344	TTTCACTCTTTGGGG[C/T]CTCATTTCTTTTCTG	55764
rs540715971	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491979	GCCATGCCTCGCTGG[A/G]TGGTATAACCTCCTG	55764
rs540779256	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129453551	GCATAGTTGTAGAGG[C/T]AGAAGAGGTGAATTT	55764
rs540860789	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481069	ACCTTATCTCTAAAA[A/T]AAATTTTTTTTAAAC	55764
rs540912957	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488105	ACAGGGTGGGCTGGG[C/T]AGGCTGGGCAGGGTG	55764
rs540932602	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482353	TTCTGCTGGGCTCGC[A/G]CCATTCTTTCTCTCT	55764
rs540964835	in-del	-/GGCTG	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129488107	AGGGTGGGCTGGGCA[-/GGCTG]GGCAGGGTGCTGATT	55764
rs540976900	snp	A/G	1.64732e-05	0.0028699	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466980	AATCCCTTCCACTCT[A/G]AAGTCAGCAGTGTAC	55764
rs541009827	snp	C/G/T			intron-variant	IFT122	GRCh38.p7	3:129488125	TGGGCAGGGTGCTGA[C/G/T]TGGCGGCTGCAGGGC	55764
rs541052355	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457471	AGGCTTTTCCTGCTT[C/G]AGGGCCTTTGCACAT	55764
rs541074818	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520562	GCCGATCTGTCAGAC[C/T]GTTAGCATGTACATT	55764
rs541122603	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501868	AGTGTAGACTGACAG[A/G]CCTCCGTGCCTTGCC	55764
rs541177232	snp	C/T	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129472037	AGGCACACATTTAGT[C/T]TGTGGTCCACCCTGC	55764
rs541225539	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509494	GGCCAAATGCGTTGT[C/T]GATGTTACGAGTTGT	55764
rs541238527	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465453	ACTTTGAGAGTAAAC[G/T]AATTATATGCTCTTT	55764
rs541289352	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129516892	CACAGACCGCTCCTG[C/T]ACACAGACACACAGA	55764
rs541289600	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477140	CCTGCATGGGTCTTC[A/G]TGGACCTTTATCCTT	55764
rs541301762	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503959	GGTGATGATGATAAT[A/G]TCAATTCTGTTTCCT	55764
rs541412481	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445870	TCGAAGTACTGTCAT[C/T]GAGAGTGTACTTCCA	55764
rs541412910	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520086	CCACTGCCAAGCCCC[C/T]TCCCCTTGAGAGGCA	55764
rs541451860	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478635	TTTTAGTAGAGACGC[A/G]AGGCTGTACTTTGGG	55764
rs541469487	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485353	CTAAGTTGATGATAC[C/T]CTCGAAACTCATGAC	55764
rs541487000	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487165	TTCTCTTCCCTGCCC[A/G]GGAAGCCAGGAGAGA	55764
rs541536810	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479391	CAGTGAGCTATGATA[A/G]CGCCACTACACTCCA	55764
rs541548656	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481099	CCAGGGATATCAGTA[A/T]ATGATAGCTATCATG	55764
rs541650885	in-del	-/TTTTTTTTTTTTT	0.285519	0.247464	intron-variant	IFT122	GRCh38.p7	3:129466496	TTTTTATTTTTATTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTGAGA	55764
rs541664769	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497398	TCAGATGGTAATAGC[A/G]ACAGCTCAGTTTAGT	55764
rs541688623	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502535	TAAAGGCCACCTCTC[C/T]CAGATCCTGGTGATG	55764
rs541690546	snp	G/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129509638	AAAAAAACATAAAGC[G/T]AGAAATGCCCGTTGA	55764
rs541701677	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129467945	AAAGAATCCTACTGC[C/T]CCAGGAGGTAAAAGG	55764
rs541779917	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129449250	ATCTAATAGGTCATT[A/G]ATTATAAAATACCAT	55764
rs541844030	snp	C/G			missense	IFT122	GRCh38.p7	3:129519582	GCAAGGTGGCTCAGA[C/G]TTCGTGCCAGTGGTG	55764
rs541871805	snp	C/G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440017	CAGCCGCCATTTCCA[C/G/T]GCTCCACCAATCAAA	55764
rs541898408	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487594	GAGAGCTGTTTCCAG[A/G]GGCTTCCAGGGTAAC	55764
rs541918093	snp	A/G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445800	AGAATTATTGTGGAG[A/G/T]TGAAATAAAATAATG	55764
rs541997876	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129466006	TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC	55764
rs542009978	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129459102	TACTAGTTGGTCCCT[A/G]TTTACCCTGCAGATC	55764
rs542028948	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129452229	TTCAGAGAAAAAAAC[A/G]GTGGTCCCTCCCCTT	55764
rs542044635	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502980	TTCAGATGGAGAGAA[A/G]CTGCCCTCGTGATGG	55764
rs542132686	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129464370	CACAAGCTAAGGGCT[A/G]TCATAGAGGTATGTA	55764
rs542142914	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452872	GGCTCAGACCTCTGT[C/G]GGGGCAGAGGAGGTG	55764
rs542152186	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129460437	ATTTACTTCCTTTTT[C/T]TTCTTTATTATTATT	55764
rs542152886	in-del	-/GTCT	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129510733	AGGAGCTAAGGGGCC[-/GTCT]TCAGACCAGCTGGGG	55764
rs542207975	snp	G/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129480005	AATGACTCTGAGCTG[G/T]GTTCTCAGGGCAGGA	55764
rs542210609	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129464498	ACTTTATGTCAGGAC[A/C]GGCAATAATGAAACC	55764
rs542214447	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493676	GGGGTTTACCTACCC[A/G]CGTGGTAAAGGGCTT	55764
rs542220313	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509177	TTGTTGTTGCATAGA[A/G]TAAGAAAAGACAACA	55764
rs542267023	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129496847	CATACTGAGATCACC[A/G]GAGTCAGTGCATCTC	55764
rs542317833	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472905	AGTTATTATTGCATT[A/T]TTCCTTTTCTAGAAT	55764
rs542426192	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468028	TATGTGGCCTCCCCA[A/G]GAGGGCTCACTGGTG	55764
rs542481033	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129497884	GGTTTTCAGAAAATT[G/T]TAAAATTACATTCCC	55764
rs542491524	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129492054	TGGCTCACTGTCTAG[A/G]TAGAGCTTGACTTCC	55764
rs542493464	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498406	GCATAGAGAATCCGC[A/G]CCATAGCAGCTGCCA	55764
rs542515775	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493611	AGCTCATGCTCTCTC[A/G]GCCACATACCCTCCC	55764
rs542550016	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129491662	CTCTGTGGTACCAGG[G/T]GCTCTGGGTCCCCTG	55764
rs542550743	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485564	CGTCATCCTTGTCTG[C/T]CCCATTACAAACCCA	55764
rs542556027	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492502	AGGATTCAGTAGGTT[C/G]TCAGGAACTGGTTTG	55764
rs542594894	snp	G/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129448547	AGCGCCATGTTGCCC[G/T]TTTCTTTACTGTACA	55764
rs542644767	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505044	GGAGTTAAAGCAAGT[A/G]TAGAACTTTCGCTGA	55764
rs542713353	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477284	GAAGATCAGAGTTCC[C/T]GGCCTCGCATAGTCA	55764
rs542746653	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489733	AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA	55764
rs542776591	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477936	CCAGTAGCGCTAAGT[A/C]AATGATGGCTTTTAA	55764
rs542794190	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129450790	CAGTGACGCGATCTC[A/G]GCTTACTGCAAGCTC	55764
rs542832406	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484906	CTAGAGTGATCTTCC[C/T]ACCCATGTTGGCATG	55764
rs542845338	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444216	ACTTTTTATTCCGCC[A/T]TGCTGCTTCTCAAAA	55764
rs542924678	snp	A/G	0	0	synonymous-codon	IFT122	GRCh38.p7	3:129514497	CCCTGCCAGATTCCA[A/G]AAGTCCATTGAGCTG	55764
rs542954128	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129471110	TACAGATTTCACACC[A/G]CAGCCAAGCAAGTGA	55764
rs542999540	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496910	ATGAACCCTTAAGGG[A/G]TCAAGACCCTAGAGG	55764
rs543006399	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458120	CTTAATCATTCTTCA[A/G]TGTGTATGTATATAA	55764
rs543008159	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441803	TTTGTACTTTTAATA[C/G]AGATTTGAGTTTTAA	55764
rs543037020	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502485	TAGCTCAGTGACTTC[C/T]GAGAAAGACACACAA	55764
rs543038694	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489241	GAAGAGAGGAGACTG[A/G]ACCAGACCAGGACTA	55764
rs543243020	snp	C/G	0.000925069	0.0214867	intron-variant	IFT122	GRCh38.p7	3:129519218	GGGTGACCTGCAGGA[C/G]GGCAGCCTCCATCCC	55764
rs543279238	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506907	CTTTACAGTAACACA[C/T]TCCAGATTCTTACTC	55764
rs543306770	in-del	-/TTTA	0.00287838	0.0378273	intron-variant	IFT122	GRCh38.p7	3:129470242	GGGTATGATTTTTTA[-/TTTA]TTTATTTATTTATTT	55764
rs543361979	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473015	TTTTAAAATTCTCAT[C/G]TGCAGCTGGGCATGG	55764
rs543395338	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129442583	AAAAAACTAAACAAA[A/C]AAAAAAAAGACAGTA	55764
rs543543256	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484775	AATGGTAAATGTTCT[C/T]ATTCTGCATGGCAAA	55764
rs543555791	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478568	CAAGCGGTCTTCCTC[C/T]TGAGTAGCTGGCACC	55764
rs543578379	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520009	AAGAAACCCCACAGC[C/T]CCCTCCCATCTCCCC	55764
rs543599464	in-del	-/AC			intron-variant	IFT122	GRCh38.p7	3:129487070	CTGGAAATTTCAAAG[-/AC]AGACAAAAGCCCCAA	55764
rs543634652	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129479580	GGGTTTGCATTGAAG[A/G]TCTGAGGCTGAATTG	55764
rs543680137	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513734	TGAAGTGGACGGGGC[C/T]GCACTGCAGACGGCG	55764
rs543705916	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482493	GGGCAGATTCAGTCC[C/T]CTTACCAGGCTCCTC	55764
rs543749503	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465339	CTTGTCAGAAAGTCA[A/C]AATTAAGTCTACAGA	55764
rs543795381	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518705	GCGGTTTCCAGGGAC[C/T]TCCAGGTGAGTCTGA	55764
rs543795502	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513076	GAGGGTGAGGGGACC[C/G]TGGGTGGGAGGGGCC	55764
rs543834622	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129484032	CCGGCAGGGTGTGTG[C/T]GTGAGTACGTGTGTG	55764
rs543855331	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129519311	CCAGATGTGGTGGCA[C/T]GAAGGAGGGGCAGGA	55764
rs543866510	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505518	TCCATCTGTCTGTGT[C/T]TGCCCTTCCAAGAAT	55764
rs543953656	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129462410	GACAGCCCCTGAGGT[A/G]TCAGGTATTATTCTC	55764
rs543984148	snp	C/T	3.33122e-05	0.00408105	intron-variant	IFT122	GRCh38.p7	3:129515464	CCTGCCCCGGCCCCT[C/T]GGGAGTCCGTGGCTG	55764
rs543991002	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519950	CTCCCCAAATCCTGG[A/G]GGCCCAGCAAGCGTG	55764
rs544128002	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501211	GCATGTGCACACACA[C/T]GTGCACATGCTGCTG	55764
rs544139676	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440700	TTCACAGTTCTTGCC[A/G]CATCCACATAGTACC	55764
rs544187052	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498931	GTATTTTGGGTAACT[A/T]CTCTGAAAAGAGGTG	55764
rs544194618	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477028	AATCCTCTCTGAAAA[A/C]TGTACCAACTCAGAA	55764
rs544237308	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129499348	GGGCATGGAGGGCAC[A/G]GAGGGCCGGCAAACA	55764
rs544249781	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494036	GCAGATCCTTAGTGG[A/G]TGCCTTTTGGATAGG	55764
rs544259444	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129506232	CACTGTACTTTTTCC[A/G]GGATGTAGCCTTGGT	55764
rs544280398	in-del	-/TT			intron-variant	IFT122	GRCh38.p7	3:129465487	TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCGC	55764
rs544349201	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129456221	TATGCTTTTCATCAC[C/T]ATCACCTGCTACCTA	55764
rs544468778	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129495764	CAAAGGACCCATCTA[C/T]AGCCACTGGTTGAAA	55764
rs544479389	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496137	ATGCCTCACGCCTGC[C/T]GGCTGCAGAGTGGCT	55764
rs544506777	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129482385	TAGGTCTTTGTAGGT[A/G]GTCAGGACTGGTTTT	55764
rs544540649	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489771	GTGAACCTGGGAGGC[A/G]GAGCGTGCAGTGAGC	55764
rs544583856	snp	C/G/T			intron-variant	IFT122	GRCh38.p7	3:129453020	GTTGGAGTTGCCCCC[C/G/T]CCACTGAGATGGAAA	55764
rs544598126	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506290	GAAGCACTGCAGATG[C/T]TCCAATGAGTGTCCT	55764
rs544609410	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129454903	CAGCAAGGGGACTCT[C/T]ATCTCCGCTCAAAGA	55764
rs544684709	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129500819	GCCTCCGATGCCAAA[C/T]GGAGGTGCTTAGATT	55764
rs544764156	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129447661	GGGATTACAGGCGCC[C/T]GCCACCACACCTGGC	55764
rs544780748	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129472081	TACTGGTGCCAGAAT[C/G]CATATTAGAATGTCT	55764
rs544787435	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129501873	AGACTGACAGGCCTC[C/T]GTGCCTTGCCTGTCT	55764
rs544805997	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440650	CTGCCTTGGATTCAT[C/T]TCACACCCACGAGAC	55764
rs544819225	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488631	CATCCTCACAAAGCT[A/G]TGAGGATCAAATGGG	55764
rs544842381	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440997	CAGGTATGATCAGAA[A/G]GGTGCTCAAAATGAG	55764
rs544919592	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496746	TGAGACCCAGGGTGT[A/T]CAGGCTCCCTCTACT	55764
rs544933969	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129490564	GCAAATCCTAGACAC[C/T]AGCACAGCTGAGCTA	55764
rs544990884	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463150	CCCCAGTGGATCCAT[C/T]TTATGTAACTATTAT	55764
rs545015832	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443403	AGGCAGGTGGAGAGA[C/G]AACCATCCTACAGTA	55764
rs545065827	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483134	AAAACAGCTATATTG[A/G]TTTTTTCTCATTATA	55764
rs545076215	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129517181	GCCTCTGCACACACA[A/C]AGAGACTGCCCCTAC	55764
rs545100578	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129509087	TTTCTCAGTCCAGCC[A/G]TGGAGCTGGTCATCA	55764
rs545117792	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482830	TACACTAGATACTAC[A/G]GTGCCTAGCTCAGTG	55764
rs545117994	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129489154	TTTTGTCCATATTCC[C/T]GGGCTGACATTGAAG	55764
rs545131069	snp	A/C/T	8.23695e-05	0.00641707	synonymous-codon	IFT122	GRCh38.p7	3:129495580	GCTTGAAATGTACAC[A/C/T]GACCTCTGCATGTTT	55764
rs545154429	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449871	TTGTCTTCTGTTCAG[C/T]ATAAATGACATCGCA	55764
rs545169623	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456917	TGAGACTTAGTCTCA[A/G]AAAAAAGGTACTTTA	55764
rs545181937	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457418	CCTCACCCTTCCCTC[C/T]GTTCCATGATGACTC	55764
rs545268036	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518320	CCAGGGCAGGCCACA[C/T]TTGCAGGCTGGACAT	55764
rs545309231	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476572	GCAGCCGCCGTGTCT[C/T]GAGTCACATCACTGG	55764
rs545324651	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129513537	TCAGGGCTATGCCTG[G/T]GGGGGCTGAGCACCT	55764
rs545369439	snp	C/G	1.64846e-05	0.0028709	intron-variant	IFT122	GRCh38.p7	3:129499899	TTTGTTGTGCTTCCT[C/G]AGGATTTCCTTGGAT	55764
rs545376043	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440087	ACCAATCGCTCGCGC[A/T]CTGGTTGCGCTGGCG	55764
rs545383841	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477861	CCAGGGTTCAGCAGA[A/G]TTGATTGTATGTATT	55764
rs545406299	snp	A/G	4.94295e-05	0.00497115	synonymous-codon	IFT122	GRCh38.p7	3:129519162	CGGAGATGAGGACCC[A/G]TTCACAGCTAAGCTG	55764
rs545413857	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440471	CAGCGGGCTTGCTGC[C/T]TGGGCCGAGGGCACT	55764
rs545498013	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129517156	CTGCCCCTGCACACA[C/G]ACGGAGACTGCCTCT	55764
rs545500708	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468017	GCCCAGAGCCATATG[C/T]GGCCTCCCCAAGAGG	55764
rs545562231	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441128	TTATCGCCTAAATCT[A/G]TAACATAGCAGTCTG	55764
rs545597439	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441582	GTCTTCCTCACTCCA[A/C]CGTCAACGCTCTCAG	55764
rs545676469	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468674	TAGATTCCCAGGTAG[C/T]TTGCTCTCCAGCCTC	55764
rs545683521	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477164	TATCCTTTCTGGTCA[C/G]AGTCACTCTGGGGTG	55764
rs545691640	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469499	TACTATTAATTATAC[A/G]TTATCATTGTTAGTT	55764
rs545749684	snp	G/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129499466	AAGATGACAGGTCTC[G/T]ATATGTGGAATTGTG	55764
rs545784885	snp	A/G	0.00874735	0.0655527	intron-variant	IFT122	GRCh38.p7	3:129516244	ACAGACTGCCCCTGC[A/G]TGCACACACAGACTG	55764
rs545881897	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482308	CAGAGAAGACAGCCC[A/G]GCAGCTCTGTGCCCC	55764
rs545912407	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129517654	GGGTCTGGGGACAGG[C/T]GGGAAGTAGGAGGGC	55764
rs545946113	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511512	TGGCCTGCTGTAATC[C/T]TCACCATCTAAAGCT	55764
rs546025883	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504955	TTCTGGCTCAGATAA[A/G]CGGGTGACTTCTGCT	55764
rs546062386	snp	A/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129461536	AGGAAGGGCCCCAGC[A/C]AAGGAAATGGTAACA	55764
rs546086796	snp	C/G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129505326	ATAGCATCTGATTTA[C/G/T]GCTTCTATATGGTAA	55764
rs546125588	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129455603	AATTCTATTCCAGGC[C/G]CAGTTCTAAGCAACA	55764
rs546161996	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452719	ATGGAACTACTGAAA[A/G]GTCCTCAGCAGAGGA	55764
rs546339211	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129455104	GACCTGAAGATTGAG[A/G]TACACTGAATTCCAG	55764
rs546361299	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491247	GCTGAGCAGAGGCTG[A/C]AAGTGGTCAGGATTG	55764
rs546395930	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453530	TTTCTCCAGCGATTT[G/T]GAGCTGCATAGTTGT	55764
rs546416018	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461691	TGTATTGACCCACAT[C/T]TATGTTTATGTGAAA	55764
rs546420958	in-del	-/G	0.00755907	0.0610114	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520385	AAGTTTGTGTTTTGT[-/G]GGGGGGGGCCTTGTG	55764
rs546424396	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129498855	GTAAGTGCTCCCAGT[C/T]TCCCTTTTTGAAAAG	55764
rs546491150	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129519250	TCTCCTGTGCACATG[C/G]GGACCCTCAGCTAGC	55764
rs546527925	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129516428	CCCCTGCACACACAC[-/A]ACAGACTGCCCCTGC	55764
rs546540924	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129468045	AGGGCTCACTGGTGG[A/G]CTGGGCTCCTGGATT	55764
rs546543875	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129487671	AGGCCATTCCAGACC[C/G]CTTCCTCCCACGAAC	55764
rs546571881	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511628	CACAGAAAATTCCTT[A/G]TTTGTCTGCTGAGCT	55764
rs546595605	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129488762	CATCACAGGCACTCC[A/G]TAAATGGCGGCTTTT	55764
rs546625729	in-del	-/TTCCTTCCTTCC			intron-variant	IFT122	GRCh38.p7	3:129459718	TCCTTCCTTCCTTCC[-/TTCCTTCCTTCC]CTCCCTCCCTCCCTT	55764
rs546629740	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129504683	CCTCTGTGGTTACTG[A/C]GCAAAGTGCTGTGCA	55764
rs546631473	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498540	GGGGCCTGTCTTCTA[C/T]TGGGTCCCAGCATCA	55764
rs546649566	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461173	AATCTTCAGTTGTAG[A/C]CACTGAAATCTTTGT	55764
rs546656803	snp	A/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129498008	CTTATCAAAATCACC[A/G]AGCATGAGAACACTG	55764
rs546683078	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499040	CCGAAGGAACACAGG[C/T]CCTAGGCCTGATCTC	55764
rs546689426	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441984	AGCTCCTGCCAATTA[C/G]CACCATGCAGGAATT	55764
rs546806197	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438767	AAAAAAAAAACCCAA[A/G]AAAACAAAAAAAAAC	55764
rs546966723	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129452407	ATGAGGGGGATTGAG[A/G]GTGCTGGGCAGGGCA	55764
rs546977982	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467281	AAATACTGAAAAGAC[G/T]AAAGGAGAAAGTTCA	55764
rs547025838	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129492648	TGGGGAGCAAGGCCC[A/G]CAGTCTGAACTGAGC	55764
rs547066668	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469090	GCTGCAGCAGTGTCC[C/T]CAGCACCATAAGGTC	55764
rs547070884	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486815	GGACATCTAAACAGA[A/G]GTTAATGGATTTACC	55764
rs547088981	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487369	TGGCTATTGCCAGCT[A/G]TTTGCTGGGACAGGT	55764
rs547097135	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129446317	GCAAGCTCCACCTTC[C/T]GGGTTCACGCCATTC	55764
rs547101760	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129453057	CAGGTAGAGAAAAGT[C/T]ATGGTTGAAGATCAG	55764
rs547102487	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520942	TCCATCCACCTTCCC[C/T]AGCCCCACAGAGCAG	55764
rs547154672	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502427	GCGTCATCTGGGTAC[C/T]TGGTAGGGGATTAGG	55764
rs547178198	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472439	CAAACTGCTGGGAAT[A/G]CAGGTGTGAGCCACC	55764
rs547211625	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515351	TGGAGCTCCTGGGCC[C/T]GGCGCCCCTTCCCTG	55764
rs547244887	snp	A/C	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129481368	TAAGCCATTGCCCCC[A/C]ACCCCCCTCTTTCTT	55764
rs547261304	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129503142	GTGGTGACAGGCACC[A/G]GGGATGTTAGTGTGA	55764
rs547305629	snp	A/C/G	0.000297897	0.012201	intron-variant	IFT122	GRCh38.p7	3:129481712	GAAGTCCCTGAGGGG[A/C/G]CCCAGGGACATCATC	55764
rs547308084	snp	C/G	0.00914312	0.0669923	intron-variant	IFT122	GRCh38.p7	3:129517243	ACACACAGAAACTGC[C/G]CCTGCACACACACAC	55764
rs547319310	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474879	TAAAGACAGGGCTGG[A/G]CATGGTGGTTCACAC	55764
rs547332856	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520368	GTGTTTCTTGCCCAG[A/C]TGAAGTTTGTGTTTT	55764
rs547347074	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129449259	GTCATTGATTATAAA[A/T]TACCATTGTTTTGTG	55764
rs547386741	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474633	GGAATGGTGTGGAGT[A/G]TAGCACCTGTGAGGA	55764
rs547424038	snp	A/G	1.67829e-05	0.00289675	intron-variant	IFT122	GRCh38.p7	3:129463507	TTGTTCCTTTTTATT[A/G]CTGGGTAGTATTCCA	55764
rs547446076	in-del	-/GAG	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129462008	ATGAAGTCACTAGAT[-/GAG]GAGTCAGAGGCCTAA	55764
rs547485100	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464229	TTCAGCATCTGTTGA[A/G]CACCTTCTACAAAGC	55764
rs547497192	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457146	CAGAGTAGGTGAAGA[C/G]CCCGTTATTTGCTGC	55764
rs547552996	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451537	TAGTGCAGAGCTGGC[A/G]TTAAAATTTAATCAT	55764
rs547558007	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457657	CAGACAAAAGGAGTA[A/C]ATTTTTGAGATCTAT	55764
rs547564658	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515748	CTCTGACGCCCACCT[A/G]CCTGACACAAGGAGT	55764
rs547587009	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454354	AACATAGTGAGACTC[C/T]CTAAAATCTGGCCTG	55764
rs547629384	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129479279	AAAAAAAAAAAAAAA[-/A]TTATTTAATTAGCTG	55764
rs547668490	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129466366	CCTGCTGTTTGATTT[A/G]TGGCTGCAGAGGACT	55764
rs547691100	snp	C/T	0.000165199	0.00908693	intron-variant	IFT122	GRCh38.p7	3:129458699	AACTTAGGTGTACAG[C/T]ATTATGAGTTTGATG	55764
rs547701924	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129485164	CTTTCTAGCTAGGTC[C/T]TTGCACCTGTCCCAA	55764
rs547705779	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129503102	GTCATTGAGAAAATC[A/G]TTACTGACAGCCAGC	55764
rs547820247	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507225	GCCTAGGTGTAAGGT[C/T]GCATTTTTCTGTTTG	55764
rs547841459	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129455836	AATATATTTACTCTT[C/T]ATTAAATGGAAGTGG	55764
rs547878798	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501663	GGTACTTGAGTAATT[C/G]AAGAAACACATTAAG	55764
rs547902125	in-del	-/A	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442097	TTAGCATCCACTCTG[-/A]AAAAAAAAACAAAAC	55764
rs547921336	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450333	CTTTTAGGCATTGGC[C/G]TATCTAAACAGTTCC	55764
rs547949366	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496513	CTACTAATGGTAGTT[A/C]TCCAGCTCACAAGTT	55764
rs547983935	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129466432	AGCAGGAGGCCCTGT[A/G]TACCTGGTGGCTGTC	55764
rs547989923	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502101	TGGGTCCCTGCAGCT[C/T]CTCCCTCTTTGGTCA	55764
rs547993293	snp	C/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129498129	TCAGGAAAGCAAAAA[C/G]CCTTTGAATTTCCAG	55764
rs548006375	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510085	TTCTCTTTTTTCAGA[A/G]ATGAGGTCTCTGTCG	55764
rs548013252	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490268	AGGCTGGATGTTACT[A/G]TTTCATCTAAATCCC	55764
rs548047124	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459390	CACCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT	55764
rs548054207	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129498577	ACAATGCGCTTTCCT[C/T]CCCTTCTTAAAATGT	55764
rs548070001	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129503285	GTAGCATTTTGGCAG[A/G]AAGCACCATCTGTGC	55764
rs548085945	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491601	CCCCTCCACCTTCTT[C/T]CAGAATCTGTCTTTA	55764
rs548156390	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438288	CAATAGCTAAGCTCT[C/T]AAGCACCAGAAAATG	55764
rs548159485	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515412	CAGCCAGGCCCCAGG[A/G]GCCTGAAGCCAGAGT	55764
rs548207177	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489280	GGCTGAGAACGAGCT[A/G]TGTCACATAAGGGGC	55764
rs548219912	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515819	AAGCTGAAGCACCCA[C/G]TCTGGGAACCTGGCG	55764
rs548311401	snp	C/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129450971	GTAATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	55764
rs548320550	snp	C/G/T			intron-variant	IFT122	GRCh38.p7	3:129514203	CTTTGGAAAAATTCC[C/G/T]GGGCCTTGCCATCCG	55764
rs548347853	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129443793	GCAAATCAGACATAT[A/G]TGATATATTTTAGGA	55764
rs548371992	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457741	GGAATAGTTTTTTTT[G/T]TTTTTTTTTTTTGAG	55764
rs548442998	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129460041	AGATACGAGCCACTG[C/T]ACCTGGCCTCTTTTC	55764
rs548498311	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452555	GGGAAGAGAGCTCTT[A/T]GCAGAGGAAGAGCCA	55764
rs548544687	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129453145	AGAACTGCTGGAACA[C/G]AGTTGTTGAGTAGGC	55764
rs548548537	in-del	-/CA	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129516003	ACACAGACACACACG[-/CA]CACACAGACTGCCCC	55764
rs548608749	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496379	AGAGGCTTCGGTACA[C/T]TGGGCAATGAGGGTC	55764
rs548615542	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502200	ACTCACCTCTTCCTT[C/T]AGAGGGCAGTCATTG	55764
rs548654116	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475117	TGAGTTATGATCATA[C/T]GACTGCATTCCAGCC	55764
rs548664989	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497140	GCAAAAAATTAGCTG[A/G]TGCCTGTAGTCCCAG	55764
rs548702791	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458474	TGCCTCCCAGTACTG[A/G]TAAGAACTAGGAAAG	55764
rs548720665	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129519489	TCACCACTGCCAAAG[A/G]TTCCAGGATCATAAT	55764
rs548736819	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469229	CAGTAAAGCTGTACA[A/G]CATTTGGCAACCTGA	55764
rs548739929	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490891	AACACTTGTTTGCCA[A/G]GTTCTGACTCTGATG	55764
rs548754891	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469226	CTTCAGTAAAGCTGT[A/G]CAACATTTGGCAACC	55764
rs548767284	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129447235	CAGAACATGTGCCCA[C/T]GGTGGTTGGGGTGCA	55764
rs548818627	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484241	GAACCACAGACAGGC[A/G]CCTGAGATTGACCTC	55764
rs548837435	snp	A/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439371	AAAAAGAAGGTGATG[A/C]CTCTTTCAAAGTAGT	55764
rs548876185	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459086	TCTTCCCCTGTTCCT[C/T]TACTAGTTGGTCCCT	55764
rs548877563	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486407	TTTCGTCAAGCCAAA[G/T]TTCTATTATTATTTC	55764
rs548880407	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492754	AGGCCTGCAGTGTGC[C/T]AAGGAAGCTGGTTGT	55764
rs548886674	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129517965	CACTCAAGTCACTTT[C/T]GCATGCAAGTGACAG	55764
rs548972369	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129449518	AGAGGGACTCAGTAA[A/G]TATCTGTGGATTTAC	55764
rs548973310	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442070	TTATGTGAAATGGCC[C/T]AATTTTTAAATGTTA	55764
rs548997168	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482871	AATGGGGCCTGAAAT[A/G]TTACTTCCCTTCTCC	55764
rs549011125	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450087	AATAGGGATGGAAAT[A/G]GGCTATTTAAAACGG	55764
rs549014260	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483762	CTTTGCTGGTGCTTT[G/T]GGGAGAGAGTAGCAA	55764
rs549033373	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514740	CCTCCTGTTCTCCCC[A/G]CAGTCCACCTGGCGC	55764
rs549062045	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444673	ACTACAGGTGTGCAC[C/T]ACCACGCCCAGCTAA	55764
rs549071527	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441137	AAATCTATAACATAG[C/T]AGTCTGTTTTGTCAT	55764
rs549174269	snp	C/T	0.00126502	0.0251179	intron-variant	IFT122	GRCh38.p7	3:129514302	CAGCACAAGCTGTGT[C/T]CCAGCCTGGGGCTCA	55764
rs549229771	snp	C/T	2.77342e-05	0.00372376	intron-variant	IFT122	GRCh38.p7	3:129478266	AATTCCATTTGTGCT[C/T]CCCCCCCAGTGATAG	55764
rs549264102	snp	A/C	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129464272	AGGGGTTGGAAGACA[A/C]CAAGTCTGTTCTTAA	55764
rs549280356	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129465571	CACCTCTCGGGTTCA[C/T]GCAGTTCTCCTGTCT	55764
rs549284542	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507273	TCTGATAGGAGCAGC[A/G]GAGGGAAGAGGCATA	55764
rs549291228	snp	G/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129470870	CTGCCACCACGCCTG[G/T]CTGGAGATGTGATTA	55764
rs549291442	snp	C/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129478673	GGCGGGAGGAATGCT[C/T]GAACCCAGGAGTTTG	55764
rs549310817	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513558	CTGAGCACCTGTACT[C/G]ATCCTTTCCAGCAAG	55764
rs549349814	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129449686	TACTGAGTGGATCAT[A/G]ATTGAATGGGCTGCT	55764
rs549352823	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490110	TCAAGCAGTCTTCTT[A/G]CCTCAGCCTCCCAAA	55764
rs549383539	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129511185	CCAGAGGAAAGGACT[A/C]CCCTGCTACCTATTC	55764
rs549385859	in-del	-/TTGGGGCAAAGCCCC			intron-variant	IFT122	GRCh38.p7	3:129477531	TTCTGGCTGTGGTGG[-/TTGGGGCAAAGCCCC]TTGGGCAGCTTCACA	55764
rs549424541	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475218	CAGGAAAATGCAAAT[C/T]GAAACCACAATGAGA	55764
rs549458200	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469137	TGAAACAGCAGATCC[C/G]AGGAAGGCTGAACCT	55764
rs549511127	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129499545	CTATGTGAGAGAGAG[A/G]CAGCCTGATCATGAA	55764
rs549554322	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505819	AGATCCTTCAAAGTG[A/G]TCATTGAAAAGCAGT	55764
rs549571881	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484993	GTGTTGTGCTTTTTA[C/T]AGCCAGCACCCCTCC	55764
rs549583365	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508152	GTCAGTGATTTGTGT[A/G]TTCTTCAGCAATTCA	55764
rs549583635	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515210	CTAATGGTGGCAGCG[G/T]CCACTGTCATTCCTG	55764
rs549737293	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129456406	CACTTTGGGAAGCCA[A/G]GGCGGGTGGATCATG	55764
rs549797581	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484388	TCCTCAGGACAGAAT[C/T]ACTCTTAAACATGTT	55764
rs549826483	snp	C/T	3.30202e-05	0.00406313	missense	IFT122	GRCh38.p7	3:129519628	CTGCGCTCCATGAGC[C/T]GCCGGGATGTCCTCA	55764
rs549929554	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464185	GTAGCTATTCTTGCT[A/G]TTCAGCTTCTAGGAG	55764
rs549941991	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477362	TGTGCTGGTTAAATA[C/G]ACTCAATCCACTTAC	55764
rs549951926	snp	C/T			intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129456179	GATCTCTAGGAATTC[C/T]GACCCAGAGACTCTG	55764
rs550058110	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457805	CAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCCC	55764
rs550080969	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502266	AGAATTCCTGCACCC[A/G]TGGTGGAAAGAGTGC	55764
rs550095622	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472304	GACTACAGGCACATG[A/C]CACCACATCCTGCTA	55764
rs550095669	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464939	TTTTTTTAATAGTCC[C/T]GCTACCTGAGAATGT	55764
rs550097949	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507074	AACACTGGCATGGAA[G/T]CTGCAGGTGACTTGT	55764
rs550105763	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465563	GCAACCTCCACCTCT[C/T]GGGTTCACGCAGTTC	55764
rs550116607	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501578	AGGCAGATTTAGGGT[A/G]CTCTGTTCTCTCTTC	55764
rs550184932	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129487618	GGGTAACTTGGAGCA[A/C]ATCACTTACCTTTCT	55764
rs550215986	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129513749	TGCACTGCAGACGGC[A/G]GGAGCAGGAACACTG	55764
rs550236478	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444545	TTTTTTTTTTTGAGA[C/T]AGAGTCTCGCTCTGT	55764
rs550239047	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129450255	CATTTTGTCCCCCAG[A/G]AAAATTCAAGCAACA	55764
rs550277025	snp	A/G	3.29451e-05	0.00405851	missense	IFT122	GRCh38.p7	3:129506486	GCCGTGGCGGAGAGC[A/G]GGTTTAATGATGCTG	55764
rs550293030	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448012	ACTTGTTATTTCTCA[C/T]TTTCATGTCTTTGCT	55764
rs550331388	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440914	CAAAACTGAACAAGC[C/T]GTAGCTAGCTATTGT	55764
rs550345526	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501020	GTGGTGAGTGTCAGG[C/T]TGGCTTTGCTCTGTG	55764
rs550377591	snp	A/G	6.58913e-05	0.00573945	synonymous-codon	IFT122	GRCh38.p7	3:129500030	AGGAGAGCACGTCAA[A/G]GCCATCGAGATCTGT	55764
rs550445254	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455447	AAGTGCTGGGATTAC[A/C]GGCGTGAACCACCAT	55764
rs550468554	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129510100	GATGAGGTCTCTGTC[A/G]CCCAAGGTGGAGTGC	55764
rs550540119	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505055	AAGTATAGAACTTTC[A/G]CTGATGTTATTAATC	55764
rs550548607	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492740	CATCCAAACCCAATA[C/G]GCCTGCAGTGTGCTA	55764
rs550560690	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499641	AACAAATGCCCATTT[A/G]TGAGACGGGAAGGAA	55764
rs550610061	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493416	TAACGTAATCTGCTC[C/T]GTGCCACATGCGTGA	55764
rs550668744	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494352	TGTCCAGCCAAAATC[A/T]ATCTTTTATCTCACG	55764
rs550707635	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439667	AGGCCCACACACTGT[C/T]CACTCTCCCGATACC	55764
rs550712574	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129517309	ACACACACAGAGACT[A/G]CTCCTGCACACACAT	55764
rs550756939	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481407	TCCTTTTCCCTGCAC[A/G]GAGCTTCTGGTGAAG	55764
rs550775733	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517827	ACCTTGGTCTTCCCG[C/T]GTGGGTCTCCCACCC	55764
rs550782719	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495064	GCTCTGTCATCCCCA[C/T]GAGCCACAACTCTGC	55764
rs550812799	snp	C/G	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129483035	GGGAGGTGATTCTCA[C/G]CCCTGCCAGGAGACA	55764
rs550841607	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488815	ATGATGCTGCACACA[A/G]TGCTGCTTTTCTTAG	55764
rs550889941	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129512212	ATAATCAGAGCCGCT[C/T]TTGTTGATGTCACTC	55764
rs550905681	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129494941	AGAACCTAGTGGATG[G/T]TCAGCATGCGGGATT	55764
rs550966225	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129446406	ATTTTTTGTAGAGAC[A/G]GGGTTTCACCGTGTT	55764
rs551003112	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129446986	ACCTGAACCAATGAA[A/G]TCCTCTGCCTGGGGC	55764
rs551013801	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487799	CAGGCCTGTAACTGC[A/G]GCACAACCTGCGATC	55764
rs551018528	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504726	TTCCCGTTTAATCCT[C/T]GCAACAGCCCTATGG	55764
rs551097372	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443918	TGTGATAATTCAACC[C/T]AAAATGACCCTTATG	55764
rs551140180	snp	A/C	0.00195046	0.0311677	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440309	GCGGGTAGGAGGAGC[A/C]CGAGCCGTAAGGGAA	55764
rs551267898	snp	C/T	0.0209421	0.100162	intron-variant	IFT122	GRCh38.p7	3:129465683	CTCTGTCGCCCAGGC[C/T]GGACTGCGGACTGCA	55764
rs551279253	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469653	ATGAGTAAACCAGAA[C/T]TCAGAGCAGTGAAAT	55764
rs551287498	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475703	CCTATGGTCCCAGCT[A/G]CTTAGGAGGCTGAGG	55764
rs551300033	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468546	ATAGGGTTTCCCCAT[C/G]TTGGCCAGGCTGGTC	55764
rs551346377	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487860	TTCCCCTGGGGTGGG[A/G]GCTTGAGGGGCTTGG	55764
rs551404508	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129497510	CACACGTGACCACAG[A/C]GTGGATTTTCATACC	55764
rs551420020	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482439	CTGGAGCCCCTCCTG[A/C]CTGGTTTCCTCGGCC	55764
rs551446184	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129448740	TCCGTCGCCCAGACT[A/G]GAGTGCAGTGGCATG	55764
rs551485551	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456337	AATATCTACTATTTC[A/C]GCTACTGTAAAAGGT	55764
rs551502987	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517373	TGGTGAAGCTGCCAG[G/T]GGGTTGAGAAGCAAC	55764
rs551529570	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129481944	AAACCGAAGGCTCTG[A/C]GCCAGCAGAGCCTTT	55764
rs551545039	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475225	ATGCAAATTGAAACC[A/G]CAATGAGATAATTCG	55764
rs551553920	snp	A/G/T	0.000164814	0.00907643	intron-variant	IFT122	GRCh38.p7	3:129512438	TCTTATCCCTCCTCC[A/G/T]TCCCACCACCGTTCT	55764
rs551565764	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129513088	ACCCTGGGTGGGAGG[A/G]GCCGGAGAGGCAGCA	55764
rs551574160	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518907	GGTGTGTGTGGCCTG[C/T]GAGGGGAATGGGTGA	55764
rs551627036	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129505660	CATATGGCAAGTGTC[A/G]TGGCTACAAGTGCTT	55764
rs551677934	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129470054	TATCTTTGAGCAGGC[C/T]ATCTTTGAGTTAGGC	55764
rs551678740	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129502508	ACACACAAGGTGGCT[A/G]ACAGGATCCTGTAAA	55764
rs551688179	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513831	GGTGACCTGAGAGGA[C/G]AGCACAAAGGCTCGT	55764
rs551754822	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499736	GAGATCACTCTTCCC[A/G]AGACCTGGGACTCCC	55764
rs551765633	snp	A/G	0.33875	0.233717	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440422	CGAGTCCTCGCGGGG[A/G]GTGCGCGAGCCGCTG	55764
rs551782653	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129480255	GAGGGAGGCAGAGAT[C/T]GTTACCTAGGTCAGC	55764
rs551785598	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469025	TGCAGCCTTGCCTAT[C/G]TTAGTGTTGCTCCCC	55764
rs551792429	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466723	GGCCAGGCTGGTCTT[A/G]AACTCCTGATCTCGA	55764
rs551797724	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455235	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCATGG	55764
rs551806128	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440708	TCTTGCCACATCCAC[A/G]TAGTACCCATACTCT	55764
rs551851622	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467194	ACTGTGGGTGAAAGC[A/G]CCTTCAAAAAAAGGA	55764
rs551875344	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475762	AAGGCTGCAGTGAGC[C/T]GTAATTGCACCACTG	55764
rs551925009	snp	A/T	2.55431e-05	0.00357364	intron-variant	IFT122	GRCh38.p7	3:129461027	TCCCCATCTCTACAA[A/T]TAAGAAAACAGTGGG	55764
rs551959920	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492823	TTTTTTTTCTTTTTT[C/T]TTTTTTTTTTTCTGA	55764
rs552081163	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129498651	CTGAAAGCAAATGAG[A/G]GAAAAAAGCGAGCTA	55764
rs552106649	snp	C/G	0.00953873	0.0683987	intron-variant	IFT122	GRCh38.p7	3:129516723	ACACACACACACACA[C/G]ACAGAGAGACTGCCC	55764
rs552113622	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462493	AGGAACCAGGGCTTG[A/G]ACTTTAGACCAGGTG	55764
rs552179340	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129446510	ATGAGCCACCGCGCC[C/T]GGCCGACCCTAGGTC	55764
rs552219857	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510514	CTGGAGAGAAACCAC[A/C]ACAAAAGGAGCCCAG	55764
rs552234287	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129510530	ACAAAAGGAGCCCAG[-/A]CTCAACTTAGGCTGG	55764
rs552297962	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497575	CTGAGGCCCCTCCTT[A/T]CACTGTGGTGGACTT	55764
rs552320830	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129445234	AGGAGGCTAAGGCAG[A/G]AGAATCGATTGAAAC	55764
rs552393097	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504553	ATCCTGGGGATGTGA[C/T]TGTTTGGTGGTGAAA	55764
rs552430033	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129453902	AACCCCAACCCAACA[C/G]CAGAGTTCTGTGAGT	55764
rs552515457	snp	C/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129460440	TACTTCCTTTTTTTT[C/T]TTTATTATTATTTTT	55764
rs552610913	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497989	AACTCTTATGTAGTA[C/T]GTTCTTATCAAAATC	55764
rs552692799	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483860	CACTCCTTGCAACCT[C/G]TGTGACTGGGGGCAA	55764
rs552694544	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129492420	GAGGCACATGGGTTC[C/T]GGATCTCTCCAGGGT	55764
rs552758002	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487000	TGTTTTGCTCTGAGA[A/G]TAGACAGACTCAAAA	55764
rs552786941	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486085	ATCCAACAGCAAGAT[A/G]AAGTATAGCTCAGAG	55764
rs552787529	snp	C/T	1.84616e-05	0.00303817	missense	IFT122	GRCh38.p7	3:129481554	ATCTTCGTGGACAAT[C/T]TCTTTGCTATCGTCC	55764
rs552848485	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486698	TGAGGAGCTGGTGCT[A/G]AGAAAATACAGTGAA	55764
rs552859463	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129481191	TTCCTGTGTTAGTTC[A/G]TGACTCAGATCTCTG	55764
rs552890578	in-del	-/A	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129462819	CAGGGCATCTGGGAC[-/A]GGGGGGAGCAAGCCT	55764
rs552903070	snp	C/G	0.33875	0.233717	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440428	CTCGCGGGGAGTGCG[C/G]GAGCCGCTGCAGCGT	55764
rs552914702	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520569	TGTCAGACCGTTAGC[A/C]TGTACATTTTGCCAA	55764
rs553105435	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446263	AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	55764
rs553106604	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439947	GCAACCGAGGTCTGA[A/C]TGTTGCGAAAGCGCC	55764
rs553108276	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129487519	GGAACTATTCATGGG[C/T]ACTCACAGCAAGGCA	55764
rs553167767	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129460228	ACCCTTCTCTCCTAC[C/G]CCCAGCCCCTGAAAA	55764
rs553205359	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472831	TCAGTATTAAATTTC[A/G]TTGACTCTTCTGCAA	55764
rs553240103	snp	A/C/G	0.000287247	0.0119811	intron-variant	IFT122	GRCh38.p7	3:129515457	ACACGTGCCTGCCCC[A/C/G]GCCCCTCGGGAGTCC	55764
rs553252573	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509657	AATGCCCGTTGAAAT[C/G]ATGTATAACATAACC	55764
rs553257503	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129488056	GCTGTGGAGCACAGT[A/G]GCCCAGTCATGAGAG	55764
rs553271958	snp	G/T	8.3053e-05	0.00644357	intron-variant	IFT122	GRCh38.p7	3:129517426	GGCGGCAAGTCCTTT[G/T]CAAGGCCTCCAGCCC	55764
rs553283982	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444650	CCTCAGCCTCCCGAG[C/T]AGGTGGGACTACAGG	55764
rs553374604	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507486	CATCCTGGAGTGGCC[C/T]TACTCCTAAGCAGAG	55764
rs553379041	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129485356	AGTTGATGATACCCT[C/T]GAAACTCATGACTGC	55764
rs553392788	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129498633	TCTGAAAGCACATTT[A/G]CCCTGAAAGCAAATG	55764
rs553411593	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490204	GTATGTGGTATATAT[C/T]TATTGTGTACAACAT	55764
rs553446736	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479429	TGACAGAGTGAGACT[C/T]TGTCTCAAAAACAAA	55764
rs553449191	snp	A/G	8.26262e-05	0.006427	missense	IFT122	GRCh38.p7	3:129514457	TGGCCCGGCACGCCT[A/G]TGACAAGCTGCGTGG	55764
rs553477072	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501902	CTCCAGACAGGGATT[C/T]GTTACAGCTGCTTCT	55764
rs553499544	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129519447	GCCACTGTTAGGGTC[A/G]CCTGGGTTTAGGAAG	55764
rs553522208	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480816	AATACCACATATTTC[A/T]TAGGGCTGTCAAAAA	55764
rs553526454	snp	C/T	6.59163e-05	0.00574054	synonymous-codon	IFT122	GRCh38.p7	3:129495562	TGGGCACGAGAACCT[C/T]GCGCTTGAAATGTAC	55764
rs553556061	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510206	ACTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	55764
rs553557958	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473595	TGTGCAGTTCTTTAG[C/T]TGTAGCTAGGCTGCT	55764
rs553627683	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502940	CCCTGGGACACAGGC[A/G]GGTGGGTACAGGGGC	55764
rs553687103	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129519292	GGAGGATTGGCCAGA[A/G]CTTCCAGATGTGGTG	55764
rs553687235	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497249	TTCCAGCCTGGGTGA[C/G]AGAGCAAGACCCATG	55764
rs553739878	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129503465	CAGAAGCAGCTGATG[C/G]TGCCCCTTCTATGGC	55764
rs553755716	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129452658	AGGATAAAGTGGTAA[C/T]AGACATGGGGTGGTC	55764
rs553816733	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489175	GACATTGAAGGAGTG[A/G]CAAAGAGGGACGTGA	55764
rs553831618	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129465100	GCACACATGTGTACG[G/T]GTACATGTATATGAG	55764
rs553892496	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450763	TCTGGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	55764
rs553895872	in-del	-/A	0.00438332	0.0466095	intron-variant	IFT122	GRCh38.p7	3:129453033	CCCCCACTGAGATGG[-/A]AAAGACTGCAGGTAG	55764
rs553922914	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496816	CAAAGACACCTAGAA[A/G]ATTTCATAACACATT	55764
rs553941972	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129496002	CCGGTCCTGCCGATC[A/G]TGCAGGACGACATGG	55764
rs553972789	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457983	GACCTCGTGATCCAC[C/T]CGCCTCAGCCCTCCA	55764
rs553988184	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483943	ATGGGAGGGGTATGC[A/C]GTGTTGTCAGCAGCG	55764
rs554000035	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484434	AGCGCTTTTCTACGT[A/G]TATATATAATATATG	55764
rs554023704	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129442299	AAAGGCAATGGCTAT[A/G]TCTTACTCGTTTCCA	55764
rs554054054	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489696	TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC	55764
rs554057538	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478288	CAGTGATAGGGTGCC[C/T]ACCTCATGGTTTTAA	55764
rs554141486	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495664	CACTGGTATTCTCAC[A/G]TGCGGTGTCCAAGTT	55764
rs554215095	snp	A/C	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129449065	AGAAAAAAATAATTT[A/C]TTGGGCTGCTTTTTA	55764
rs554218069	snp	C/G	0.000148651	0.00861994	missense	IFT122	GRCh38.p7	3:129519710	CTGACGCCTCCATTA[C/G]CATGTGCCCCTCCTG	55764
rs554220473	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508689	ATACTTTGGGATTTG[A/G]CGAACTCTTGGAAAG	55764
rs554254219	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441589	TCACTCCAACGTCAA[C/T]GCTCTCAGCCACTAC	55764
rs554298190	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465202	TTTCCTTATGAATCA[A/G]TAGTGGAGCTCTTTG	55764
rs554361432	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458053	AGGAATAGATTTTAA[A/G]TGTTCTCACTATAAA	55764
rs554380614	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129478222	ATCCTGTGCCAGGTG[A/G]GCAGCAGCATGTTGA	55764
rs554396928	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477889	ATTAGATACTCTAAA[A/G]ATTTTTCAATGAGAG	55764
rs554418963	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492310	AGAGCTCACTGGCGT[C/T]TGGGCATCTGGGCCA	55764
rs554439910	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129444831	GGCCAAGTTTACACT[C/T]TTTAACAATTCTTAA	55764
rs554460537	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129470403	TGAGTAGCTGGGACT[A/G]CAGGCGCCCACCACC	55764
rs554492795	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490613	AGAGGGTGTCAGTAG[C/T]AGGCCCCTTTCCACA	55764
rs554564820	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129509427	AGCCTCTCATCTCCT[A/T]TGCAAAACTTCTTGA	55764
rs554576762	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456744	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	55764
rs554642445	snp	C/T	0.215144	0.247558	intron-variant	IFT122	GRCh38.p7	3:129465791	GGGACTACAGGCGCC[C/T]GCCACCGCGCCCGGC	55764
rs554654606	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129458873	TGGCCACTTACTGGC[A/G]TGGCCAGCACTGGGC	55764
rs554676547	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443093	TAGGCCACATGTCCA[C/G]ATGTCTTTATAGGTG	55764
rs554677020	snp	A/G	8.24165e-05	0.00641883	missense	IFT122	GRCh38.p7	3:129502803	TGGACAGCCCTGGCT[A/G]TGCTGCTGAGACCTA	55764
rs554719261	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129484546	ACTTTTATGTGTATA[C/T]GTATTGCTACCTATA	55764
rs554725025	snp	A/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129451280	ATTTTTATTTTTTTT[A/T]ATTTTTATTTATTTT	55764
rs554762108	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129451780	GTTTTTGGTTTTGCA[A/G]TGCAGTTTTTATTGG	55764
rs554801284	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471134	CAAGTGAGAAATGCA[A/G]CCTGTGCAGTGAAGC	55764
rs554843798	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129507954	CTGCCATGCATCAAG[A/C]AGTGGGCTCCTGAAT	55764
rs554858796	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471869	TTAATAATAATAATA[A/G]CTAACATTTATTGAA	55764
rs554860543	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129494212	TTTTTTGTTTGTTTG[-/T]TTTGTTTTTTTTTTG	55764
rs555001895	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129496100	GTCAGGCAGAGCCTC[C/T]GCCCTCCCATGTTAG	55764
rs555014066	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496612	CCTGTTCGACCCTGG[A/G]GCTGAAGGTGTGTTT	55764
rs555019632	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518691	ACTGTGGGAGAGGGG[C/T]GGTTTCCAGGGACCT	55764
rs555041014	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488973	ATGAAAGCTAGAGAG[A/G]TGGCTGAAAACATCT	55764
rs555082088	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518934	GTGAGGGCAGCAGGG[C/T]CAGCAGAGTCCCTTC	55764
rs555221460	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513861	TCAGCCTCTGGCTGA[A/G]GAGCTTCAAGGGGGC	55764
rs555247199	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456830	CTGAGGCAGGATAAT[C/T]GCTTGAACCCGGGAG	55764
rs555257593	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129463447	GTTTTTTCATTCAGC[A/G]TAAAATCCTGGAGAT	55764
rs555277675	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520447	TGCCTTGTAAATAGC[A/C]CCAGGAGATGAGGAA	55764
rs555281580	snp	A/C/T	9.92481e-05	0.00704381	missense	IFT122	GRCh38.p7	3:129514528	GGTACCCTGACCATC[A/C/T]GCGCCAAGCCCTTCC	55764
rs555286600	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506689	GCCTGCCTTGCAGTG[G/T]CGTAATCTGGTGTAT	55764
rs555341083	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514970	CTCCCAACCCACATT[C/G]CTTCAACCCAGCCAG	55764
rs555352694	snp	C/T			synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460890	ATTGCACCTCCATCT[C/T]CCATTTCTGGGCCTC	55764
rs555354353	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504850	GTGGCAGGGAGGTAA[C/T]GTGAGCCAGGGTACC	55764
rs555441218	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483258	CAAAAGTAATACTTG[C/T]TTACTCAAAAATTCC	55764
rs555455625	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476932	GTTAGCCACTGGGTC[C/T]GTGTCTTGTTTTCTT	55764
rs555478908	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129513325	CAGCTCCTTCCCAGC[C/T]GCAGCCCCACCTTCC	55764
rs555491121	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506187	TTTTCAAAGTCAGTC[A/G]CCTTTTCCCAGCCAA	55764
rs555501079	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512570	TGTTTGGCTATAGAG[G/T]CTCAGCAGGGAGGCC	55764
rs555515051	in-del	-/TGTGTGTG			intron-variant	IFT122	GRCh38.p7	3:129465148	GTGTGTGTGTGTGTG[-/TGTGTGTG]GTGTGTGAGTGATGC	55764
rs555518874	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477652	GTCTTCCCCGTTTGT[C/G]AAGGAGGTGGGCAGG	55764
rs555562948	snp	A/C			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440476	GGCTTGCTGCCTGGG[A/C]CGAGGGCACTGAACC	55764
rs555565010	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457682	ATCTATTGCACAGCA[C/T]GGTGACCATAGTTAA	55764
rs555582459	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461977	TATCAGTCTGTGTTC[A/G]TTGCTAGTGGATACA	55764
rs555602838	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129495372	TCACTTGAAATAGCC[A/G]CATCTAACCTTTGTA	55764
rs555617428	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505179	CGAAGAGGCTAAATG[C/T]GCCATGCCAAGTCAC	55764
rs555630826	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470142	GAAGGAATGAAAATA[A/T]ATGACAGTTCAGAGA	55764
rs555685724	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511896	CCTAAGCTGCATAGA[A/C]GGTCTTCTCTTTTAG	55764
rs555760522	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513946	GTGCAGACAGAGTGG[A/G]GTACACCCAGGGGCC	55764
rs555845930	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129446000	GCTCTTTTAAAATTT[A/T]ACCTGAGAGACTGTT	55764
rs555867862	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483834	GGGCCTGGAACCTGC[C/T]GCCCTGTCTCCACTC	55764
rs555872675	snp	A/G	0.000399281	0.0141238	intron-variant, missense	IFT122	GRCh38.p7	3:129506766	GGGTTATGGTTGGCA[A/G]GTCCAGCCCTGCATT	55764
rs555883105	snp	A/G	0.000399281	0.0141238	missense	IFT122	GRCh38.p7	3:129514391	CTGTTCACGGCAGGA[A/G]AATACTCTTCACCTT	55764
rs555897183	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507366	CTTGGGTCTTGCTGC[A/G]GCTGTCGCTCCCCCA	55764
rs555947193	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129498052	ATCACTCAGCACAGC[C/T]TCTTTCTGTCCACTT	55764
rs555951185	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129470417	TACAGGCGCCCACCA[C/G]CACGCCTGGCTAATA	55764
rs555963191	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455286	CAAGTGATTCTCCTG[C/T]CTCAGCCTCCTGAGT	55764
rs555990954	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488601	TCTCTATAGACGTAG[C/G]ATGATGACAGGCCCC	55764
rs556053346	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129448697	TTTATTTATTTATTT[A/T]TTTTTTTTTTTTGAG	55764
rs556070984	in-del	-/T	0.0205511	0.0992634	intron-variant	IFT122	GRCh38.p7	3:129465974	ACCACACCTGGCTAA[-/T]TTTTTTGTATTTTTA	55764
rs556110198	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477106	GATGATTTATGACAG[C/G]TTGGAGCCAGGTGGT	55764
rs556141264	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474860	TGGAATATATAAAGA[A/G]CTATAAAGACAGGGC	55764
rs556180686	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457354	TTTAGGATAAAGAGC[A/G]AGGCCTCTGCTGTGT	55764
rs556200824	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129450548	ATCTCCATTCTTTGT[A/G]TGGTTAACTACATAA	55764
rs556217320	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129496722	TTAGTGATTTCTTCA[C/T]TCCGTACCTGAGACC	55764
rs556299164	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129506032	TGCAGTAAAGTGGCA[A/G]GTCCTGTTTCTATCA	55764
rs556316611	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463776	CTTTCTTCGTCTCCT[C/T]GATGGGAAAGACTTG	55764
rs556317075	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129501228	TGCACATGCTGCTGC[A/G]GTAGGCAAAGGACAC	55764
rs556344810	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489086	GGCTTCCAACCTCCA[C/G]TCCCCTACCCCTTCC	55764
rs556357888	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456882	GATCGTGCCACTGCA[C/T]TATAGCCTGGGCAAC	55764
rs556410412	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489614	GGAGGCCGAGGTGTG[C/T]GGATCACAAGGTCAG	55764
rs556415692	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500381	TTTTCCACCTATGCC[A/C]TCAGGGCTGGTGTCT	55764
rs556426424	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129464413	GGAGCTCAGAAAAAG[A/G]CACCAAATGGTGCCT	55764
rs556485305	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518715	GGGACCTCCAGGTGA[G/T]TCTGACCCGCCCTGG	55764
rs556495210	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446656	TTTGATTGAAGTCTC[A/G]TGTTTCACTAAAATG	55764
rs556615115	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129455300	GCCTCAGCCTCCTGA[A/G]TAGCTGGGACTACAG	55764
rs556631003	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440019	GCCGCCATTTCCACG[C/T]TCCACCAATCAAATC	55764
rs556670159	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440452	GCAGCGTGTTTGAGG[C/G]GGGCAGCGGGCTTGC	55764
rs556711820	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448457	TAGGGCTAGGTGTGT[C/T]ATTTGCATTGGGTGC	55764
rs556750566	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129448952	CTTCCTCCTGCCTTG[C/G]CCTCCCAGAGTGCTG	55764
rs556889655	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441528	TGGATAATTTGCCAG[C/T]GTCACACAGTGAGGG	55764
rs556926471	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442124	AAACACCGTGTGGGC[C/T]AAATAAAACATTTGC	55764
rs556970717	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129462297	GGAGAAGGTGGGATT[-/A]AAAAAAATATAATAT	55764
rs556991567	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493039	CCCAGGCTGGTTTCA[A/G]ATTCGTGGGCTCAAG	55764
rs557015676	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129516119	ACACACACAGACTGC[C/T]CCTGCACACACAGAG	55764
rs557074997	snp	C/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129516848	CTGCCCCTGCACACA[C/T]ACACACACAGAGGCT	55764
rs557159295	snp	A/G/T	3.29462e-05	0.00405857	missense	IFT122	GRCh38.p7	3:129517546	CTCATCGACCTGGAG[A/G/T]TGCTGAGACCCAAGC	55764
rs557200841	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129512078	AAATCATCTATCTAG[G/T]TGTCGGTTTCCTCAT	55764
rs557214887	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129510268	GCCCTGCCTTCCACC[C/T]TGGGCATTTCTTTCC	55764
rs557227242	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503636	TTCACTGAGAGGAGC[C/T]GTCTGACTGTTGTCT	55764
rs557234686	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484766	GTGTCAGTAAATGGT[A/G]AATGTTCTTATTCTG	55764
rs557271652	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518071	AGCGCTCAGTCTGGT[C/T]GGTCACAGGCTGGCT	55764
rs557273469	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512118	GAGGATAAAAATGCA[C/T]ACCACAAGGTTATTA	55764
rs557285069	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440496	GGCACTGAACCCCGG[C/T]CTGGGAGACTGCAGG	55764
rs557302808	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459561	CTTGTGTCCCTGATA[A/C]AATGCCTAGCCCATA	55764
rs557308771	snp	C/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129486910	CCTATGCCTGCTGCC[C/T]CGCTAAAGGGAGCAT	55764
rs557450247	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490917	TGATGCCTCCCTTAA[C/T]GCTGCCTCCCACCCC	55764
rs557484899	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510917	ATCCCTCAGGGGAAA[C/T]GTTTAGAGGCCTGTG	55764
rs557488968	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129518772	TGCTCCATCACAAGT[G/T]CCCGCAGACCCCCAG	55764
rs557512128	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466805	ACTGCACCTGGCCCC[C/T]AGGGGCTCCTTGCCA	55764
rs557512180	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474335	TCCCTAAAGTTATTT[A/C]TTTTATAAATTGAAT	55764
rs557629252	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518613	CTCCAACTTGGTACC[A/G]GCAGTCCCCATGTCC	55764
rs557655027	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462781	ATGTTGTCTAGACAT[A/G]CACTTGCTATGAGGC	55764
rs557690666	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513259	TTTTTAAGGTCTTGG[A/G]TGTCAGGAGACATAA	55764
rs557696452	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129476864	TGGAAAGGGCTGGTG[A/T]CAGGGCACTTGAAAT	55764
rs557720239	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498788	AGTACTCTCCACAGG[C/G]TACATTATTCCTGAG	55764
rs557751155	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511099	GCATCCAGGGCCCAG[C/G]AGAGCAGCACTGATT	55764
rs557765165	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129488042	GGCAGAGAGTTTGTG[C/T]TGTGGAGCACAGTAG	55764
rs557828344	snp	C/T	0.0263992	0.111815	intron-variant	IFT122	GRCh38.p7	3:129488524	TTAGGCTGACCTGGG[C/T]TTGTATCTTAGCCAC	55764
rs557840832	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482600	TGGCCACCTCTAGCC[C/T]AGAGGTAACTCCATG	55764
rs557849930	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476193	CACAGGAGAAAAGGC[C/T]GGCCAGCTCTCCCTG	55764
rs557852403	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473851	TTCTTCTAAATGTGC[A/C]TGTGTCTTCAGTTTC	55764
rs557882787	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518119	ACTGTCCTCTGGGCA[A/G]CTTCATTCTTTGGCA	55764
rs557926018	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504742	GCAACAGCCCTATGG[C/T]ATAGCTACCATCATT	55764
rs557945079	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512845	CACCAGGTGGCAAAG[C/T]TGCCATCAAAGAGGG	55764
rs557958999	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468692	GCTCTCCAGCCTCAG[A/G]CAAGGGAGTTTCTCC	55764
rs558060952	snp	C/G/T	0.0047834	0.0487097	intron-variant	IFT122	GRCh38.p7	3:129498859	GTGCTCCCAGTTTCC[C/G/T]TTTTTGAAAAGCTCC	55764
rs558083491	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482814	AGAATTGCTACAGGA[A/G]TACACTAGATACTAC	55764
rs558090091	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129516875	GGCTGCCCCTGCACA[C/G]ACACAGACCGCTCCT	55764
rs558099852	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472715	TAATTACACTTACAT[C/T]AGACCTTTTGTTACT	55764
rs558117421	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129506106	GAACCTCACTGAAGA[C/T]GAGCAAGTTTCACTC	55764
rs558125845	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129455069	GTCTTTTAGTCCTCA[A/G]AATTGGTTTTTTCCT	55764
rs558166657	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129459034	CTTGGGGTCAGTGTG[C/G]TCCAGGCCTCCTCTT	55764
rs558179879	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474424	GCAGCAAAAAACTCC[A/G]GTGGTAATAAGGAAC	55764
rs558187547	snp	A/C	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129498303	AGTCCCTTTGAAGGA[A/C]ATTTCTAGTCTCCTA	55764
rs558263203	snp	A/G	1.66682e-05	0.00288684	intron-variant	IFT122	GRCh38.p7	3:129502890	GGGATGAGGTGAGGG[A/G]AAAGCAGGCCTCATG	55764
rs558310013	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129492362	GTGGCCACACTGGGG[A/G]AGACAACAGCAGGTA	55764
rs558383101	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513191	TAAGCAGAGCAGGTG[C/T]CTGAAGGGCCTGTGC	55764
rs558389458	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129479119	AAATACTATTAAAAT[C/T]TCTCAAAAGCCTAGA	55764
rs558441680	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447528	AATGTTTCTTCTCAC[A/C]CTGCAAAACAGAGTC	55764
rs558477183	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443240	GGGGCTGGGTCAGAT[G/T]ATGCAGGAATTGGAG	55764
rs558530542	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129503424	ATTAGCCAGGTCAGC[A/G]AGAAAGGTGGCCAGC	55764
rs558543614	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481028	CTGTGAATAGCCACT[A/G]CGATCAGCCTGGGCA	55764
rs558576589	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513163	GTAGCCATCGAGGGC[C/T]ACAGTGGTACCATAA	55764
rs558618358	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444081	TCCACAAGTGTCAGG[C/T]GCTTTGGATAGACTG	55764
rs558623841	snp	C/G	0.00953873	0.0683987	intron-variant	IFT122	GRCh38.p7	3:129516307	ACACACACACACACA[C/G]AGAGACTGCCCCTGC	55764
rs558635274	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452635	AGAATCGGGAATTGT[A/C]GAGGATGAGGATAAA	55764
rs558671918	snp	C/G	0	0	intron-variant	IFT122	GRCh38.p7	3:129445724	ACATCAGGCAAACTA[C/G]TTGACCTCTCTGAGC	55764
rs558704073	snp	C/T			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507343	CCCAGCAGGCTCTTC[C/T]GACACATCTTGGGTC	55764
rs558829529	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520531	CCGAGTTGTTCGTGG[C/T]AGCCTGCTGGAGTCC	55764
rs558845714	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465893	ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	55764
rs558866035	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450980	CCACCTCGGCCTCCC[A/T]AAGTGCTGGGATTAC	55764
rs558921825	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485815	AGGCCATCCTGCTGA[C/T]GCAGCGGGTCAGGAC	55764
rs558989772	snp	C/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129480394	GGCCAGTTAGATGTG[C/G]GATATCCAGGTTACA	55764
rs559098879	snp	A/T	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129481072	TTATCTCTAAAAAAA[A/T]TTTTTTTTAAACCAG	55764
rs559154036	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515084	TCTCCTAGCTCTGTC[C/T]CCATCTTTCTGCACC	55764
rs559154908	snp	A/G	0.000131852	0.00811842	intron-variant	IFT122	GRCh38.p7	3:129479762	CTGTTGAATTTCCAT[A/G]CAGAGCTGGGTTTGC	55764
rs559164626	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129473928	CAGAGTTTATTGTTG[C/T]TACTTTGTGGGAAGA	55764
rs559166900	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472749	CTCCAAGTCATCGAG[G/T]CCCTGTTATTATTTT	55764
rs559183873	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515759	ACCTACCTGACACAA[A/G]GAGTCACTGTCGGTG	55764
rs559216783	snp	A/G	0.000139421	0.00834813	intron-variant	IFT122	GRCh38.p7	3:129515440	AGTCCAGGGGGAGGA[A/G]GACACGTGCCTGCCC	55764
rs559220027	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439142	AACTAGAATTAGAAT[C/G]AAGGTTTTCTGATGT	55764
rs559261478	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503889	TAGGTGAGAAGCAGT[C/G]AGTGGGTCCATACAG	55764
rs559262392	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444978	GACATATGCCAACAA[A/T]GATAATGGCAGCCAC	55764
rs559303154	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486347	CACTCTTTGGGGCCT[C/T]ATTTCTTTTCTGTGA	55764
rs559327738	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466379	TTGTGGCTGCAGAGG[A/C]CTTGGTGGCTCTAGG	55764
rs559372462	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129459059	CCTCTTACTATTGGG[G/T]ATCTGCCGTGTTCTT	55764
rs559410973	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457245	TTATATGTTGCCTCT[C/G/T]TCCAGTCTGTTCCTT	55764
rs559437280	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457671	ACATTTTTGAGATCT[A/G]TTGCACAGCATGGTG	55764
rs559462969	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129516538	ACACACAGAGACTGC[C/T]CCTGCACACACACAG	55764
rs559531676	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471220	TTTAGATGTGTGTAG[C/T]CCAGCTTTTGGGCCA	55764
rs559549573	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458381	GACAGCTACATGTAG[C/T]AGGCTCCCAATACAT	55764
rs559670499	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500857	AGTGAGTGACCACCT[A/G]CAGTCAGACACCCCC	55764
rs559680830	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506856	GCACTGGGTTTTAAA[A/T]TTTTTTAATTAAATG	55764
rs559739409	snp	C/G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457959	TGGCCAGGATGGTCT[C/G/T]GATCTCCTGACCTCG	55764
rs559753087	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472083	CTGGTGCCAGAATCC[A/G]TATTAGAATGTCTAT	55764
rs559762890	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129478647	CGCGAGGCTGTACTT[C/T]GGGAGGCTAAGGCGG	55764
rs559775366	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515148	GCTAAATGAGCCAGT[A/G]TAGTCCACGTGCTCC	55764
rs559813946	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129465497	TTTTTTTGAGATGGA[A/G]TCTCGCTCGGTTGCC	55764
rs559836090	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509097	CAGCCGTGGAGCTGG[A/T]CATCACGGTTGTCAT	55764
rs559862199	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129507937	TTTGATTGACTGTTT[C/G]TCTGCCATGCATCAA	55764
rs559973706	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129489176	ACATTGAAGGAGTGG[C/G]AAAGAGGGACGTGAT	55764
rs560013262	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449994	CCTCCCTCTTGTGAG[C/T]ACTCTGAAATTTGAC	55764
rs560016406	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496304	CTTCTGTGGGAAGGA[G/T]TTGCACTAAGGAGCC	55764
rs560049476	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129442623	AAATCCTAGATGTCA[A/G]AGATTAGTCCTCCAC	55764
rs560115247	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129488743	CCTGACTAGTAGCCT[A/G]GCACATCACAGGCAC	55764
rs560128880	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129442681	TGCTCCTTTGCTTCT[A/G]TTTTAACCTTCACAT	55764
rs560176500	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129482839	TACTACAGTGCCTAG[C/T]TCAGTGTTGAGCACA	55764
rs560179270	in-del	-/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129446860	ATGGGTTGGGTTTTG[-/T]TTTTTTTGTTGTTGT	55764
rs560190032	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520104	CCCTTGAGAGGCAGT[A/G]CGTCCTGGCCCCAGG	55764
rs560218010	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129463951	AGCTTTCCCTCCCAC[A/T]CTTTGATGCTAGACC	55764
rs560218054	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456349	TTCAGCTACTGTAAA[A/C]GGTACTTGGCCGGGT	55764
rs560277091	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129494881	ACCTACCCTGAGGGT[C/T]ACTGAGAGGAATAAA	55764
rs560278472	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456959	TTAGTTGACTCCCAT[A/T]AAAAGACTCTGAGGA	55764
rs560293728	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483423	GTATTGGGCTGAAAT[G/T]TGTGAGCGCTGACCA	55764
rs560390826	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129484165	CAAGCTCTCTGAACC[A/G]GGAGGTGGCCAGAAC	55764
rs560415998	in-del	-/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129516910	ACAGACACACAGAGA[-/C]CGCTCCTGCACACAC	55764
rs560452077	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484872	CTAGTTTCCCCCAAC[A/G]GTAACAGTGTGCATA	55764
rs560454315	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518748	TCAGCAGGGACTCTC[A/G]CCCCTGTCTGCTCCA	55764
rs560481171	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501796	ATGCCACCTTTCCCT[A/G]AAAACGTGTCCTTTT	55764
rs560575789	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469543	CATTTGCTGTGGTAC[C/G]AGATACTGTGCTCAC	55764
rs560637122	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518384	TGGCCTGAGGCCTCG[C/G]TCCCTTGCACTGACT	55764
rs560700319	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129513097	GGGAGGGGCCGGAGA[A/G]GCAGCAGGACCCAAG	55764
rs560748218	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491420	GGGCAGAATCTGAAA[A/G]CAGCAAAACTAGCTT	55764
rs560782455	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463203	GAGACTGGCACAAAG[G/T]GTGTATATTATATAG	55764
rs560853255	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129448511	AATCTTTTATTATGC[A/C]GTTGGGTTATTTACG	55764
rs560856018	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490629	AGGCCCCTTTCCACA[A/G]AGAAGATGGTTGGAG	55764
rs560907993	snp	A/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129450101	TGGGCTATTTAAAAC[A/G]GGCAAGTAAACTATC	55764
rs560964567	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129451690	TGGTTCTCAAGGATT[C/G]GTAGTATATTCCTGG	55764
rs560971417	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457569	TCTCCACTGAAGGAT[C/G]TCATCCTTAGAGAAA	55764
rs560985444	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443488	GCTAGATGGCCATCT[A/G]TAAGGAATTCTTGCC	55764
rs561022468	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444217	CTTTTTATTCCGCCA[C/T]GCTGCTTCTCAAAAT	55764
rs561027663	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485613	AACTCATCTCCCTCA[A/G]TTGCCCCAAACTAGC	55764
rs561069322	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478687	TTGAACCCAGGAGTT[A/T]GAGACCTGTCCAGCT	55764
rs561083404	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441855	TTATTATAAACGTAC[C/T]TATAGCACAAGCTGA	55764
rs561129160	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477943	CGCTAAGTAAATGAT[A/G]GCTTTTAATTTCTCT	55764
rs561136209	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479555	CCTCTGGCCTAGGCT[G/T]CCTGGGTGGGGGTTT	55764
rs561151491	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509679	AACATAACCACATTT[A/G]AGAATGTATTCTACT	55764
rs561204396	snp	G/T	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129456013	TAGTTAAAACTCATG[G/T]TGTTCAGGGGTCAAC	55764
rs561311201	snp	A/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129518167	TAACACAGAGATGTC[A/T]GGAGCAGTGCCAGCC	55764
rs561360722	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129518776	CCATCACAAGTGCCC[A/G]CAGACCCCCAGCAGC	55764
rs561380306	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464065	TCCTCATCTGACAGA[C/T]AGGGATAAAAATACT	55764
rs561403287	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506911	ACAGTAACACACTCC[A/G]GATTCTTACTCATCC	55764
rs561436843	snp	A/G	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129513639	GTGCCATCCCCTGGG[A/G]ACCTGGAAATGGCTC	55764
rs561441986	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457067	TGCCCTGTGAATAAA[G/T]TCTAAAAGTCCTTAA	55764
rs561582437	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468752	CAGCACTGATCCCCA[C/T]AGGTTCTCAGTTTCA	55764
rs561631741	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448632	CCAGGTAGCCTTTTT[C/G]TATTGGCACAGCTGC	55764
rs561640261	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129456071	TTAATCTTCACACCA[A/G]CCATGAGGTAAATAC	55764
rs561645828	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464499	CTTTATGTCAGGACC[A/G]GCAATAATGAAACCA	55764
rs561667562	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449121	TCTTTTACCTTCACT[A/G]TCTGGCTAAATAATT	55764
rs561698295	snp	A/G	4.94205e-05	0.0049707	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504401	TAGCAGAGAACGATC[A/G]CTTTGAGGAAGCCCA	55764
rs561706696	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498544	CCTGTCTTCTATTGG[G/T]TCCCAGCATCAGGGT	55764
rs561707472	snp	A/G	0.000165117	0.00908468	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476328	AGATTGGAAAGGATC[A/G]GGCACTGAACTTTGA	55764
rs561769174	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468501	AGACACGCGACACCA[C/T]GCCGAACTAATTTTG	55764
rs561777668	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461745	TCTTGTGCAATTTGT[C/T]GTCATTACTGGTTTA	55764
rs561812855	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499620	GAAAGTGTTGTTTAG[C/T]CGATGAACAAATGCC	55764
rs561825107	snp	A/G	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129499995	GAGCCCAAAGCCGCC[A/G]TGGAGATGTACATCT	55764
rs561887793	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129494983	CTTTAGAAGTAGGGA[C/T]ATCGTAAGACTTGTC	55764
rs561887851	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129500735	GGTTGGAATAAAAGA[C/T]GTGTGGGAATGGGAG	55764
rs561965141	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492720	GCTGAGAATATTGAC[C/T]TTGTCATCCAAACCC	55764
rs561968596	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129460795	CGGGTTGAGACGCCT[G/T]GCATGGTACATGATT	55764
rs561998553	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495712	TGCGGACAAAAACTA[A/G]CAATGGTCTCAGAAA	55764
rs562024511	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446370	GCTGGGACTATAGGT[A/G]CCCGCCATCATGCTT	55764
rs562037136	snp	C/G	0.0178098	0.0926698	intron-variant	IFT122	GRCh38.p7	3:129517301	ACACACACACACACA[C/G]AGAGACTGCTCCTGC	55764
rs562052408	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488770	GCACTCCGTAAATGG[C/T]GGCTTTTATTATCGG	55764
rs562100319	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129451272	TCCACCTAATTTTTA[-/T]TTTTTTTTATTTTTA	55764
rs562128555	in-del	-/A	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457696	ATGGTGACCATAGTT[-/A]ATAATAGCGTATATT	55764
rs562153242	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488130	AGGGTGCTGATTGGC[A/G]GCTGCAGGGCTGCTC	55764
rs562166070	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129451310	TTATTTTTTGTAGAG[A/C]TGGGGTTTCACTTAG	55764
rs562183480	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446930	AGTAACCTTAACAAT[A/G]GTCTGTTTTGACAGG	55764
rs562276866	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481882	CACACAGGCACAAGC[C/T]GCAGGGCCTGGACCG	55764
rs562341429	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474944	GAGATCACTTGAGAA[C/G]AGGAGTTCAGGACCA	55764
rs562341523	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482363	CTCGCGCCATTCTTT[C/T]TCTCTTTAGGTCTTT	55764
rs562348439	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441208	TCATTCAGCATTGTT[A/G]TGAAGCCTCTGTTCT	55764
rs562419432	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441953	ATGCTCGGCCTAAAA[A/G]GGGCAGCTGCTGCTC	55764
rs562435603	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461454	AGGCTGACAGTTATT[C/T]TTTAAATTGTGTGGA	55764
rs562455593	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468895	GTTAATTTTCTTTCT[G/T]CAGGAAGAGCAAGCA	55764
rs562459994	snp	A/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129442584	AAAAACTAAACAAAA[A/C]AAAAAAAGACAGTAG	55764
rs562463599	in-del	-/CA/CACA	0.102726	0.202016	intron-variant	IFT122	GRCh38.p7	3:129516321	CAGAGACTGCCCCTG[-/CA/CACA]CACACACACAGAGAC	55764
rs562467634	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456272	TGGAAATAGTAAGAG[C/T]AGTTTCTTTGTTTAT	55764
rs562474345	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129497430	ATGAGATTTGCACAG[A/C]ATAATGTATAGGAAA	55764
rs562564072	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129455451	GCTGGGATTACAGGC[A/G]TGAACCACCATGCCT	55764
rs562669542	snp	A/G	0.00199481	0.0315187	intron-variant	IFT122	GRCh38.p7	3:129498844	AGACCTGGGCTGTAA[A/G]TGCTCCCAGTTTCCC	55764
rs562676487	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488244	CTTTTTTTCCCTTGA[C/T]GAAATCCTGCAGTCC	55764
rs562677161	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489369	GGGGTGGTGAGAATG[C/T]CCGCTGCAGTCATGA	55764
rs562691898	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496195	GAGATTCCCTTTTGC[A/T]TTGGGACGGCCCCCA	55764
rs562767571	snp	C/T	1.73399e-05	0.00294443	synonymous-codon	IFT122	GRCh38.p7	3:129483599	GTGCACCGGCAGAAG[C/T]TGCAGGGCTTTGTGG	55764
rs562776056	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129454905	GCAAGGGGACTCTTA[A/T]CTCCGCTCAAAGATG	55764
rs562804895	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489775	ACCTGGGAGGCGGAG[C/T]GTGCAGTGAGCCGAG	55764
rs562825310	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518248	GCTGTGGCAGTGAAA[A/G]CCCCGGGGCACAGCT	55764
rs562887889	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513077	AGGGTGAGGGGACCC[C/T]GGGTGGGAGGGGCCG	55764
rs562951063	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447695	TTTTTGTATTTTTAG[C/T]TGAGACAGGGTTTCA	55764
rs563014749	snp	A/G	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129476518	TGTGGTAAGAAGAGA[A/G]AGTTTGTTCTGTGGG	55764
rs563093728	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482418	AGAGTGAAGTTCCCC[C/G]CAAAGCTGGAGCCCC	55764
rs563125331	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474718	CTGAGAGAATGACCT[G/T]GGGGGCTGAGCTCGG	55764
rs563188760	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467958	GCCCCAGGAGGTAAA[A/G]GGGGGTTGAAAATCA	55764
rs563205920	snp	A/G	0.000399281	0.0141238	missense	IFT122	GRCh38.p7	3:129481590	AAGCAGGCCACAGCT[A/G]TGCGCTGCTTGGACA	55764
rs563325732	snp	C/T	0.00302205	0.0387543	intron-variant	IFT122	GRCh38.p7	3:129459366	ACGATCTCGGCTCAC[C/T]GCAAGCTCCACCTCC	55764
rs563355936	snp	C/T	0.0209421	0.100162	intron-variant	IFT122	GRCh38.p7	3:129516616	CACAGAGACTGCCCC[C/T]GCACACACACACACA	55764
rs563418416	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510459	TGGCTTTCCTGAAAC[A/G]AGACCCCCTCAGGGT	55764
rs563461166	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129461144	AAAGTCAGAGGCTGT[A/G]GGCTCATTATTAAAA	55764
rs563478528	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504931	TGAGAATAGAAACTC[A/G]GCTTCTATTTCTGGC	55764
rs563499183	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458506	AGCTAACACTTACTA[A/G]GTACCTTAAAGAACT	55764
rs563507667	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129455407	CAAACTCCTGACCTC[C/G]TGATCCGCCCACCTC	55764
rs563579853	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504483	CTGCCAAGACATACA[C/T]TTCAGGAAGGCTACC	55764
rs563600850	in-del	-/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129501487	CTTGTCCGATAGTAA[-/T]TTTTTTAAAGACAGA	55764
rs563620269	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445177	CCAAAAATACAAAAA[A/T]GACCTGGGTGTGGTG	55764
rs563621387	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129453824	TAAAATAAATCCATG[G/T]TGTCCCACAGCATAG	55764
rs563654119	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129472160	CATATGTCTGATTTT[A/G]TTTACTTTTTGAGAA	55764
rs563658329	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129446125	TACAAACTCTCCTCT[C/G]TAAAGCCTAGTACCT	55764
rs563717272	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472960	TTATTCATTACAAGC[A/G]TATTTTTCTTTATAG	55764
rs563731670	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466021	ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTTCT	55764
rs563774157	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129516072	CACACACAGACTGTC[C/T]CTGAACACACACACA	55764
rs563783688	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509695	AGAATGTATTCTACT[A/G]TCAAACAGCAAATTC	55764
rs563810995	in-del	-/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129490844	CCCATGTGATGCCCG[-/C]CATTGCCCTTTTCTA	55764
rs563822123	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452958	TGACAGATTGGATAT[A/G]GGCTATGAAGAAAAA	55764
rs563847138	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502999	CCCTCGTGATGGAAG[C/G]AACATTGGGCTGGCA	55764
rs563858836	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486673	CAAGACTGGAGAGCC[C/T]GGGAGATGGTGAGGA	55764
rs563892555	snp	G/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129498433	GCCAGAAGGAAAGGT[G/T]TGTCTGTAAAGGCCC	55764
rs563894428	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492089	CCTAGCCAATCACCC[A/G]CTTTTGAAGCCAAGA	55764
rs563909337	in-del	-/A	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129470099	TGGTGTTTCAGGCAG[-/A]AAAAAAAAATAGCAT	55764
rs563965454	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461597	TTGCTGCCTTTGGGA[A/G]GCCTTCCCTTGGTGT	55764
rs564027164	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129455036	GCCTCTTCATGACAC[A/C]TGTATAATGATTAAG	55764
rs564041015	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455364	TTTCAGTAGAGACAG[C/G]GTTTCACCATGTTGG	55764
rs564081614	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517170	ACACGGAGACTGCCT[C/T]TGCACACACACAGAG	55764
rs564098386	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510327	TTTTTTGCCTCTTGG[A/G]AAAGTCTGGCAAGAA	55764
rs564146700	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474818	GAGAAGTTTTACAAC[C/T]CATATATCTGATAAA	55764
rs564156412	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511569	ATATACAGTGTGCCA[A/G]ATGCCTTCAAAATAA	55764
rs564158826	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468026	CATATGTGGCCTCCC[C/T]AAGAGGGCTCACTGG	55764
rs564234578	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454592	AGAATAATGTTTTAG[A/G]GAGACCTGTGAGGAG	55764
rs564281304	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520021	AGCCCCCTCCCATCT[C/T]CCCTTCCAGCCCTCA	55764
rs564320223	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499477	TCTCGATATGTGGAA[G/T]TGTGCACCAGGTTGT	55764
rs564331960	in-del	-/G	0.00517822	0.0506191	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440310	GGGTAGGAGGAGCCC[-/G]GAGCCGTAAGGGAAG	55764
rs564339008	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129497995	TATGTAGTATGTTCT[C/T]ATCAAAATCACCAAG	55764
rs564343956	in-del	-/T	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129460432	TCAGAATTTACTTCC[-/T]TTTTTTTCTTTATTA	55764
rs564416762	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439304	AGCTCTACCAGCTGT[A/G]AGTTTAGCAGCAAGT	55764
rs564452282	snp	C/T	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440101	CTCTGGTTGCGCTGG[C/T]GCCTTAGGGGCTCCA	55764
rs564533351	snp	A/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129459925	CACCAGGCCAATTTT[A/T]AAATTTTTTTTTTTC	55764
rs564599516	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441659	TGTCTGCAGGAGACA[A/G]GCAGGTAACATAAAT	55764
rs564600380	snp	G/T	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129446868	GGGTTTTGTTTTTTT[G/T]TTGTTGTTGTTTGTT	55764
rs564604595	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129485618	ATCTCCCTCAATTGC[C/T]CCAAACTAGCTCTGC	55764
rs564698686	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449118	GACTCTTTTACCTTC[A/G]CTATCTGGCTAAATA	55764
rs564703269	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129446475	CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	55764
rs564713079	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515241	CCAGGGGAAAAGTGC[C/T]GTTGAGCGCTGCCTG	55764
rs564812792	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473725	TCCCACTTCACTTTC[C/T]GGGTGCTGTGGTCCT	55764
rs564908375	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479601	GGCTGAATTGGGCTC[C/T]GTGGGGAAGCCTTGC	55764
rs564911557	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443535	ACTGCATGACAAGGT[C/T]TAGAGTCCTTTCCAA	55764
rs564932802	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129502012	CCAGAGAGAACAAGC[A/G]CATTCTATCCAGGCC	55764
rs564952157	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444265	TCAGAGGAAGAAAGC[A/G]TAAGAAACAAGGAAG	55764
rs564982524	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129474128	GTATTAAACTTATAA[C/T]TGCAGTTTAAATTGG	55764
rs565019473	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129499235	CAACTAACCAGAGAG[A/G]TGTTTGCTTGTTATC	55764
rs565104576	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129519328	AAGGAGGGGCAGGAC[A/C]CCTTCCTGTGGGGTG	55764
rs565122563	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471159	TGAAGCCTTTAATTG[C/T]GTAGCATCCTTATTC	55764
rs565131217	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484040	GTGTGTGTGTGAGTA[C/T]GTGTGTGATGGTGGT	55764
rs565137710	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129501432	TGTGTGGGCCCCTCA[C/T]AAAGGGACCTTGATG	55764
rs565145381	snp	A/G	0.000399281	0.0141238	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478028	CAGTTCGGATTAAAT[A/G]CAAAGAGCTTGTCAA	55764
rs565172203	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515680	TCTCTGGCCTCAGGA[C/T]GTTGGGCAAGGGCCA	55764
rs565191638	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466195	ACGAAAGGTCCTACT[G/T]GTTTACCAGCTCAAT	55764
rs565219340	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129480305	TGGATTAAGGCAGTG[C/T]GTTCCAGCATGTGTC	55764
rs565259969	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458242	CTCTTTCATAGGATC[C/T]GTGTCTTACCATGTT	55764
rs565327949	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129483184	TATAAAAGATTTAGT[C/G]ATTATAAAAGATCCT	55764
rs565339774	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479653	GCCAATCGTGGGGTC[C/T]ACATTGGGTTAGATA	55764
rs565352604	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129478597	CCACAGGCACATGCC[A/G]CCACACCCAACTAAT	55764
rs565360805	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520010	AGAAACCCCACAGCC[C/T]CCTCCCATCTCCCCT	55764
rs565361250	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514221	GCCTTGCCATCCGAG[A/T]AGTACACTCACCTCT	55764
rs565400476	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457645	GGTAGTTTCAGTCAG[A/G]CAAAAGGAGTACATT	55764
rs565437247	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129507819	TGAGCTAGGGGTCCC[A/G]GGCATATCTAAAGAG	55764
rs565464032	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129464227	CGTTCAGCATCTGTT[C/G]AGCACCTTCTACAAA	55764
rs565468787	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496964	TGAGGCCTCCTCAAG[A/G]AGGCAGCTGTGCTGC	55764
rs565504126	snp	A/G	0.000395563	0.0140579	missense	IFT122	GRCh38.p7	3:129502772	CTGCTGCTGTGCGCT[A/G]CCTACCTCAAGAAGC	55764
rs565609331	snp	A/T	0.0170251	0.090679	intron-variant	IFT122	GRCh38.p7	3:129465136	GTGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGTG	55764
rs565615362	snp	C/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129503176	CGACAGCTCCAGTGC[C/G]TGCTGTTGGGCTGAG	55764
rs565623381	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497656	TTGCTCCGTCTCTCT[A/G]TGAAGGTAAATACTC	55764
rs565633890	snp	A/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456710	ACCTGAGGTCAGGAG[A/T]TTGAGACCAGCCTGC	55764
rs565672906	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484352	CGTGCATAGCGAGAA[A/G]CTGTAGCCTTCAGCA	55764
rs565754661	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129460593	GAATATTATTCCATT[A/G]TATATATAGACCACA	55764
rs565755863	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515378	CCTGCCTGCCCACCC[A/G]GGTGGCCTTTCCTCT	55764
rs565769093	in-del	-/T	0.00597247	0.0543191	intron-variant	IFT122	GRCh38.p7	3:129510681	GAGGGCTCCTGTCTC[-/T]TAACAGCTGAGCTCT	55764
rs565769894	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509335	ACTTCTCCTGTAGTT[A/G]TGAGAGGATCAGCTT	55764
rs565778639	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456811	GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAT	55764
rs565790799	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457150	GTAGGTGAAGACCCC[A/G]TTATTTGCTGCCATG	55764
rs565844045	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450386	CATATTTTCAAATAA[C/T]ATAAGCTCCCTCTGG	55764
rs565916911	snp	A/T	1.65693e-05	0.00287826	intron-variant	IFT122	GRCh38.p7	3:129463532	ATTCCAACCAATCCA[A/T]CTTCTTTTATATTAT	55764
rs565931610	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485048	TGTATTTACAGCTGC[A/G]TTTTATTGTGTCTTG	55764
rs565949719	snp	A/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129451711	ATATTCCTGGTCACA[A/T]AGTACATAGACCTGG	55764
rs565987945	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452423	GTGCTGGGCAGGGCA[A/G]GGGGTTGGGTACAGT	55764
rs566042437	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507226	CCTAGGTGTAAGGTC[A/G]CATTTTTCTGTTTGG	55764
rs566164903	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501667	CTTGAGTAATTCAAG[A/G]AACACATTAAGCATG	55764
rs566225729	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129497109	AATATGGTGAAACCC[C/T]CTCTCTACCAAAAAT	55764
rs566285596	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490776	CAGATCTAGAGGGTG[A/G]TGTGTAAGACCTACA	55764
rs566296139	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495321	AGACAACAGCCAGGA[A/G]CCAAGCCCAGGTTCC	55764
rs566340770	in-del	-/GG	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519948	TCCTCCCCAAATCCT[-/GG]GGGCCCAGCAAGCGT	55764
rs566346759	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443719	TGTAAAGAAGACTGT[A/G]TAAGTCAGAGCTAAA	55764
rs566358347	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488921	TCATGGCGGGATTCA[C/T]GGACTTGATTCGTTG	55764
rs566392739	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448754	TGGAGTGCAGTGGCA[A/T]GATCTTGGCTCACTG	55764
rs566393441	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520369	TGTTTCTTGCCCAGA[G/T]GAAGTTTGTGTTTTG	55764
rs566417104	snp	A/G			utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520490	ATATTTTCTAAGGAA[A/G]AAAATCTGTTACTTT	55764
rs566421503	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441985	GCTCCTGCCAATTAC[C/T]ACCATGCAGGAATTT	55764
rs566455545	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518271	GCACAGCTCAGCCTG[C/T]CCCTTGGCCAGGAGG	55764
rs566514306	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465690	GCCCAGGCCGGACTG[C/T]GGACTGCAGTGGCGC	55764
rs566517446	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129481966	AGAGCCTTTCTTAAG[C/T]GTTTACCATGAACAA	55764
rs566529239	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482501	TCAGTCCCCTTACCA[G/T]GCTCCTCCTTGTTCT	55764
rs566584599	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442014	TTGGCCTAGTGTGCT[C/T]AGCTCTTCCTGTTTT	55764
rs566614366	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129511777	GTTTGGTGGCACATC[A/G]GTCAAGCTGCTGTTG	55764
rs566636487	in-del	-/TTTTTATTTTTATTTA	0.0287284	0.116357	intron-variant	IFT122	GRCh38.p7	3:129451276	CCTAATTTTTATTTT[-/TTTTTATTTTTATTTA]TTTTTATTTTTTGTA	55764
rs566637469	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438290	ATAGCTAAGCTCTTA[A/G]GCACCAGAAAATGCT	55764
rs566661917	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129463097	TAGTAAGTTACAAAG[A/T]TGGTACCAAGAAGTC	55764
rs566676607	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477563	GGGCAGCTTCACAGT[A/G]TCCCCCTTAGGGACA	55764
rs566687266	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129505128	CTGAGCACTTAACCT[A/G]TGTAACCTTGAATCT	55764
rs566761808	snp	A/C/T	9.88093e-05	0.00702815	intron-variant	IFT122	GRCh38.p7	3:129514261	ACAGAGCCTTCCTCA[A/C/T]GGTCTTTCCTCTGCC	55764
rs566774874	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129506650	TAAAGCCCTGGGCTT[A/G]TTTATTGGGTGTATT	55764
rs566811334	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499742	ACTCTTCCCGAGACC[C/T]GGGACTCCCCCAACT	55764
rs566819251	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475763	AGGCTGCAGTGAGCC[A/G]TAATTGCACCACTGC	55764
rs566853210	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512492	CTTCCAGAGCACTTT[C/T]CTGGCAGAACCTTCC	55764
rs566864008	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475242	AATGAGATAATTCGC[A/G]CTCACTAAAATGGAG	55764
rs566879352	snp	A/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129469144	GCAGATCCCAGGAAG[A/G]CTGAACCTCAACTCT	55764
rs566886399	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517376	TGAAGCTGCCAGTGG[A/G]TTGAGAAGCAACTCT	55764
rs566924994	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468187	ATGACATTTGCCACT[C/G]TTGGCTGGGTTTTAC	55764
rs567018522	snp	C/G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129519029	CTGCCCTTGAGTCTT[C/G/T]TCACAGGGGTGTAGG	55764
rs567030576	snp	C/T	9.91408e-05	0.00703993	missense	IFT122	GRCh38.p7	3:129519604	CCAGTGGTGGTGAGC[C/T]GGCTGGTGCTGCGCT	55764
rs567107794	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129489576	AGGCGCGGTGGCTCA[C/T]GCCTGTAAATCCTAG	55764
rs567111493	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129461965	TGTTTTCAGCTCTAT[C/T]AGTCTGTGTTCGTTG	55764
rs567123601	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129455236	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCATGGC	55764
rs567123795	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462549	AGCACTGCTGAAGGA[G/T]GCCCAGGAGGAAGGA	55764
rs567186131	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455554	GAAAAACAATATAAT[A/G]TGAAGAAATAATAGA	55764
rs567261453	snp	C/T	3.30153e-05	0.00406283	missense	IFT122	GRCh38.p7	3:129519631	CGCTCCATGAGCCGC[C/T]GGGATGTCCTCATCA	55764
rs567316167	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476042	GGCGGAGGAGCCCTG[A/G]CACACTCCTGCACTC	55764
rs567387031	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484334	ATTGCCATAAAACAG[A/T]GACGTGCATAGCGAG	55764
rs567413216	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129465965	TTTTGTTGCCACCAC[A/T]CCTGGCTAATTTTTT	55764
rs567421594	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464382	GCTGTCATAGAGGTA[G/T]GTACAGAGGGCTGGG	55764
rs567468176	snp	C/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129478271	CATTTGTGCTCCCCC[C/G]CCAGTGATAGGGTGC	55764
rs567480409	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129470999	TCAGAAGAATAACTT[G/T]TTTCCATGGAGGGTG	55764
rs567530119	in-del	-/AGTA			intron-variant	IFT122	GRCh38.p7	3:129449513	ACCTAAGAGGGACTC[-/AGTA]AGTATCTGTGGATTT	55764
rs567537425	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471435	ATCATTCAACAGATA[A/C]TTATTGGCACACCTA	55764
rs567557062	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129508093	CTCCTTCAGTAGGGC[A/G]AAGGCCCAGATTAAC	55764
rs567658836	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506021	TTACCTCCAAGTGCA[C/G]TAAAGTGGCAGGTCC	55764
rs567658968	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468624	GCTGGAATTACAAGC[A/G]TGAGCCATCACGGGC	55764
rs567719816	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461983	TCTGTGTTCGTTGCT[A/G]GTGGATACAATGAAG	55764
rs567741939	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505187	CTAAATGTGCCATGC[C/G]AAGTCACAAATCTAG	55764
rs567769798	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452737	CCTCAGCAGAGGAGG[A/G]ATCTGATTTGATTTG	55764
rs567813993	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454455	GCAGCAGATTGGCCC[A/G]AAGACAAAACTAATT	55764
rs567821556	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447372	TTAAACATTTTCTGG[A/C]TGACAATTGGCTGAG	55764
rs567833817	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455162	GATTTCTCCTTTAAG[G/T]TCATTAAGTTTTTTT	55764
rs567893501	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463295	ATGCAGTTACCACTT[A/G]GTGTCATATCTACTC	55764
rs567930757	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129504699	GCAAAGTGCTGTGCA[C/G]TGCAGTGTATCTTCC	55764
rs567965259	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449521	GGGACTCAGTAAGTA[A/T]CTGTGGATTTACTGG	55764
rs568008750	snp	G/T	1.65241e-05	0.00287433	intron-variant	IFT122	GRCh38.p7	3:129461190	ACTGAAATCTTTGTG[G/T]TTTGCTGCATAGTAA	55764
rs568030127	snp	A/T	0.0437281	0.141251	intron-variant	IFT122	GRCh38.p7	3:129460447	TTTTTTTTCTTTATT[A/T]TTATTTTTTTTTATG	55764
rs568032582	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129498774	TGAGGCTGACACAAA[G/T]TACTCTCCACAGGGT	55764
rs568068237	snp	C/T	0.000161747	0.00899151	intron-variant	IFT122	GRCh38.p7	3:129459434	AGCTGGGACTATAGG[C/T]GCTCACCACCATGCC	55764
rs568085726	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129492944	CCACCTAGCCTCCCA[A/C]GTAGCTGGGACCACA	55764
rs568110992	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452347	TAAATTAAGTAGTAT[A/G]CTGGAAGGTGATAAC	55764
rs568185693	snp	A/G	9.88484e-05	0.00702954	missense	IFT122	GRCh38.p7	3:129488371	ATGGAAGCGCTAGAA[A/G]GTTTAGATTTTGAAA	55764
rs568204500	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129487937	AAATAGGTATTTTCC[A/G]GAGGCAGAGTGGGGA	55764
rs568232748	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129484617	GTAAACAAGACTTCT[C/T]ATCCCTTCCTTTATG	55764
rs568254468	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129511538	AAGCTTTATTAGAAA[C/T]GGGCAATCTCAGTTT	55764
rs568287377	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440440	GCGCGAGCCGCTGCA[C/G]CGTGTTTGAGGGGGG	55764
rs568301822	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482515	AGGCTCCTCCTTGTT[C/G]TCAGCAGCAGAATCG	55764
rs568344360	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129487633	AATCACTTACCTTTC[G/T]TGGACTCAGTCCCTG	55764
rs568379714	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517942	TCGGTGTTGGCCCCC[A/G]GCTCTTCCACTCAAG	55764
rs568466059	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129486890	CTAGGTCACCTGCTC[C/T]GTAGCCTATGCCTGC	55764
rs568477663	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129516048	ATACAGAAACTGCCC[C/T]TGCACACACACACAC	55764
rs568483709	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439454	ACGTAGTCTAATGAC[G/T]TCCTAGGATCCTCCA	55764
rs568575935	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129448163	ATGCTGTTGAAGCGG[C/T]GTCATTGTCTGGGGT	55764
rs568611610	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440915	AAAACTGAACAAGCT[A/G]TAGCTAGCTATTGTT	55764
rs568664298	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511641	TTATTTGTCTGCTGA[A/G]CTTCTGGCAGCCTCT	55764
rs568664908	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129473599	CAGTTCTTTAGCTGT[A/G]GCTAGGCTGCTTGGC	55764
rs568668865	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129481375	TTGCCCCCCACCCCC[C/G]TCTTTCTTTTGATGA	55764
rs568678988	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129474236	GCCTTAAACAGTCAA[A/G]GTCAATTGGCTGTTC	55764
rs568713469	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129499647	TGCCCATTTGTGAGA[C/T]GGGAAGGAAGCACTG	55764
rs568714891	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441769	TTCTTGAAACACAGC[C/T]GTATCAGTGAATCTT	55764
rs568792687	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465768	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	55764
rs568857816	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461850	TTACAGCACTGGTGT[A/G]GTACTGGCACAAAAG	55764
rs568871804	in-del	-/A	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440457	GTGTTTGAGGGGGGC[-/A]GCGGGCTTGCTGCCT	55764
rs568916580	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129444772	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAATGCT	55764
rs568935551	snp	A/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129448705	TTTATTTATTTTTTT[A/T]TTTTGAGACGGAGTC	55764
rs569004008	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488492	GGAGAGGCCATAGAC[C/T]GCAGCAGTCTCTGGA	55764
rs569004148	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129495186	TTGGAATACACAGGA[A/G]AGCAACCCTGAGGAA	55764
rs569016913	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129517322	CTGCTCCTGCACACA[C/T]ATACAGAGACTGCCC	55764
rs569025683	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129482569	GAGCAGCCTCAGTCA[A/G]TTAGAAGGAGTTACC	55764
rs569057224	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518575	ATATGTGCTATGGTG[C/T]TGGCAGGTGGGTGCT	55764
rs569064034	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488880	TCTCTGATTCTGACA[C/G]CAATGTGGGCACTTC	55764
rs569144244	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518863	GCTCACAGGGCCCGC[A/T]TGTGCTTCCCACTGG	55764
rs569182953	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129513234	GATCATTACCAGGCA[A/G]TGATCCAGATTTTTA	55764
rs569199625	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129512208	CTCAATAATCAGAGC[C/T]GCTCTTGTTGATGTC	55764
rs569232059	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452176	GTATTTATTGAGGTC[A/G]TCTATGTTCCAGGCA	55764
rs569319585	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450283	ACAGGACTGACGGTG[C/T]TGTGTCCATGAAAAG	55764
rs569322159	snp	A/G	0.220246	0.248223	intron-variant	IFT122	GRCh38.p7	3:129465798	CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT	55764
rs569352757	snp	C/T	9.55064e-05	0.00690971	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440326	GAGCCGTAAGGGAAG[C/T]CGTGATGAGGGCCGT	55764
rs569354859	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475569	AGGTAGGAGGATCAC[A/G]TGAAGCTGGGAAGTG	55764
rs569358127	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129498111	ATAATGTGTAACTTA[A/G]CTTCAGGAAAGCAAA	55764
rs569384690	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466588	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	55764
rs569403951	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129499557	GAGACAGCCTGATCA[C/T]GAACCCCCGACCCTG	55764
rs569494846	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505072	TGATGTTATTAATCA[C/T]ATTTTTTAAAGTTGA	55764
rs569507011	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461246	CAATGATGCTATACA[A/G]TGTGTCTCCTACAAT	55764
rs569532956	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492334	TGGGCCACAGCCTTG[C/T]TCCGGGGGCAGAGTG	55764
rs569546047	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129480436	GTGTGTGTATACATG[C/T]GTACACGTGTGTTCT	55764
rs569574516	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499155	TGCTGTCCCACTGTC[G/T]GATCAGGTTCTCACC	55764
rs569641025	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129515834	CTCTGGGAACCTGGC[A/G]CAGGGCTTTACATAA	55764
rs569644029	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129492820	GCTTTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTC	55764
rs569645337	snp	G/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507206	ACAGTTTGAAAATTG[G/T]CAAGCCTAGGTGTAA	55764
rs569714390	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129510099	AGATGAGGTCTCTGT[C/T]GCCCAAGGTGGAGTG	55764
rs569780776	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450972	TAATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	55764
rs569817482	snp	C/G			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504104	GTGTTGTTACTGAAT[C/G]CAGTCGCTTGCATAT	55764
rs569818635	snp	A/G	0.00114876	0.0239387	intron-variant	IFT122	GRCh38.p7	3:129459391	ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	55764
rs569819977	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129451489	GACTTTCAAATTCTT[A/G]GTAGCAAATATGAAA	55764
rs569931518	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445632	AGCAGAAGGCAGCAT[A/C]GCGCGTTAATTACAA	55764
rs569945407	in-del	-/CT	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476206	GCTGGCCAGCTCTCC[-/CT]GTCTTCCCAACTCCC	55764
rs569956437	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129444526	TAATGTAAGTTTACA[C/T]TCTTTTTTTTTTTTG	55764
rs570090189	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466735	CTTGAACTCCTGATC[G/T]CGAGCGATTCACTTG	55764
rs570109093	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485196	TTGGCGCCTTGGCAT[A/G]AATTCCTAGAAATGA	55764
rs570152122	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467248	TGGGTATAAAGTGAT[C/T]CTGTGAGAAACTATA	55764
rs570163676	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129460206	TATATCCTTCAAATA[C/G]CTACTCACCCTTCTC	55764
rs570209046	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129490972	GTGTTCTCCAGGCAT[C/G]TGGTTCGTAGTTGGA	55764
rs570252241	snp	A/C	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129485914	CTGTGGTTTTGGCCC[A/C]GAGAGGAGGGAGAAA	55764
rs570327741	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487466	GACTGTGGGGACAGC[C/T]AAAAGCCTTTTATAA	55764
rs570328438	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129474055	CATCAGATAAGTGCT[A/G]GGGAAAGTTTTCGTT	55764
rs570362884	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479720	GGGACAGAAAGATCT[C/T]CTTGGGGAGGTCTGG	55764
rs570422634	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441702	TTTGCATCTTCAACA[C/G]TAGGAATTGTATGTT	55764
rs570436275	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510576	TCAGCCTCACTTTGC[C/T]CAAGCCACTCCAGAG	55764
rs570439368	snp	C/T	0.00835141	0.0640778	intron-variant	IFT122	GRCh38.p7	3:129487873	GGGGCTTGAGGGGCT[C/T]GGGAGGACTCTGCAG	55764
rs570510180	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465311	ATAGCTTTTTCATGA[A/G]CCTTTTTTTGCCCTT	55764
rs570510188	snp	A/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439050	TCCTAATCACTAAAC[A/C]ACAGATTGTAAAAGG	55764
rs570529787	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129489732	TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG	55764
rs570541754	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129453323	AGGAAGCAACAGCAA[C/T]TGAGAGTGGCAATGG	55764
rs570546829	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129462186	TTTAACATATTTTAT[A/G]GCATTTTCTTCATGT	55764
rs570548878	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129504064	TTTCCGATTCTGTGC[C/T]GCTTCTGTGGTCCAG	55764
rs570564922	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129517712	TGAGCCTGGCCCTGT[C/G]TTCCCAGAGAGATTG	55764
rs570566134	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498660	AATGAGGGAAAAAAG[C/T]GAGCTAATTGTTCAA	55764
rs570566794	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493564	GTCCATAGCCAAAAA[C/T]TTGGTGGAATTCAAG	55764
rs570642088	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129447065	TTTCTCCATGTTCTA[A/G]CAACATCTTGCACAT	55764
rs570723932	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129514712	TGCCAGCTCCCCTGT[G/T]CTTCCCTGTCCACCT	55764
rs570731270	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129469661	ACCAGAACTCAGAGC[-/A]GTGAAATTATATGCC	55764
rs570744897	snp	A/G	0.000144742	0.00850589	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439881	CGCCGCAACGCCCAG[A/G]GTGTGGGGCGGAGTA	55764
rs570768113	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129494982	TCTTTAGAAGTAGGG[A/T]TATCGTAAGACTTGT	55764
rs570784128	snp	G/T	0.33875	0.233717	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440424	AGTCCTCGCGGGGAG[G/T]GCGCGAGCCGCTGCA	55764
rs570857738	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445553	ATGTGTTCAATAAAT[C/G]TTAGTCACTGTTATT	55764
rs570871473	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491761	CAGTCTCTCATCAGT[C/T]CATGCATCTCATCCT	55764
rs570873048	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129451687	CTTTGGTTCTCAAGG[A/G]TTGGTAGTATATTCC	55764
rs570904364	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484405	CTCTTAAACATGTTG[A/G]AATACATCTGCTTAG	55764
rs570916534	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485036	CCCCACCTGCCTTGT[A/G]TTTACAGCTGCATTT	55764
rs570960896	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466587	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	55764
rs571045170	snp	C/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129486778	ACATCTCTCCTTTGC[C/T]CATGGTAGCCTGAGC	55764
rs571068976	snp	C/G	0.0379877	0.132479	intron-variant	IFT122	GRCh38.p7	3:129516725	ACACACACACACACA[C/G]AGAGAGACTGCCCCT	55764
rs571116822	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469948	GGTGTGGTATGTGAC[A/G]CAATAGAAAGCTGTA	55764
rs571121909	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129515873	CCCAGAAAGAGAGTC[C/T]GATGGCTTTGCATTC	55764
rs571156327	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478275	TGTGCTCCCCCCCCA[G/T]TGATAGGGTGCCCAC	55764
rs571194249	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444981	ATATGCCAACAATGA[C/T]AATGGCAGCCACATA	55764
rs571217403	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471066	ATTAGTAGGCAGGAA[A/G]TGCCAAGGATTAGAG	55764
rs571359564	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463392	CATTCAAGAATGTTA[C/T]ATAAATGGAATCGTA	55764
rs571395283	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471510	CAAATAACCACACTG[C/T]AGTGGGAGGGAATGG	55764
rs571427820	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129502378	ACCTCTTAGGGTGGT[A/G]AAGATTCTGATTTCA	55764
rs571508311	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465053	ACAGGCCAAAGTGTG[A/T]GTGTGGCGTGTGTGT	55764
rs571509958	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129502636	CAACACTGGGGACCA[C/T]AGAATGAATGGACAT	55764
rs571594517	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129477428	GTGCACTGCTAGGTG[C/T]CTTTGCAAGGGATCC	55764
rs571664093	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129456569	TTGAACCTGGGAGGC[A/G]GAGATTGCAGTGAGC	55764
rs571700840	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129495981	ATCGGTGTCTTCAGG[A/C]AGGAGCCGGTCCTGC	55764
rs571758870	snp	C/G	9.88338e-05	0.00702902	missense	IFT122	GRCh38.p7	3:129517586	GACAGCTAGAGATTG[C/G]AAACAACAGTATCCA	55764
rs571804753	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129501907	GACAGGGATTCGTTA[C/T]AGCTGCTTCTCCTTC	55764
rs571872530	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129450279	AGCAACAGGACTGAC[C/G]GTGCTGTGTCCATGA	55764
rs572014110	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129464487	TTGATCCTCTGACTT[C/T]ATGTCAGGACCGGCA	55764
rs572034396	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482101	TGCCTGTGTCTATGC[A/G]CACCTACAGCGTGGG	55764
rs572036055	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507592	AGTACTGTTGCCTGG[C/T]CCCTCCTCCTGGGGC	55764
rs572095841	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453028	TGCCCCCCCCACTGA[A/G]ATGGAAAAGACTGCA	55764
rs572126179	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129514922	TGCCCTTTCTGGAAC[C/T]AGGCTGTAGTTCTCC	55764
rs572148936	in-del	-/A	0.319856	0.240042	intron-variant	IFT122	GRCh38.p7	3:129442579	AACAAAAAACTAAAC[-/A]AAAAAAAAAAAAGAC	55764
rs572163106	snp	A/C/G			intron-variant	IFT122	GRCh38.p7	3:129513188	CCATAAGCAGAGCAG[A/C/G]TGCCTGAAGGGCCTG	55764
rs572176942	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129443456	TGAGCTCCCAGCCCT[A/G]GAGTGTTCAAGCAGG	55764
rs572251844	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457996	ACCCGCCTCAGCCCT[C/T]CAAAGTGCTGGGATT	55764
rs572255539	snp	C/T	0.000131917	0.00812043	intron-variant	IFT122	GRCh38.p7	3:129483442	GAGCGCTGACCAAGC[C/T]CAGGGTGGTTCTCAC	55764
rs572267700	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483969	CAGCGTGTGTTTTGC[A/G]GAGAGCCCAGCGTGG	55764
rs572282768	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503800	GAATGACTCAGACCT[C/T]GCTGTGCATCAGGCA	55764
rs572325626	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129477928	TTTAATTGCCAGTAG[C/T]GCTAAGTAAATGATG	55764
rs572349624	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129485484	GCAAGAGGAAGAAGG[A/G]AATGAGGTGGGTGGA	55764
rs572380246	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449100	AAGGGAAGTTCTGCC[A/G]AAGACTCTTTTACCT	55764
rs572419476	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441745	AGTCTTGTATTCTGT[A/C]CCCCATTTTTCTTGA	55764
rs572422360	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485280	GGTTTCCCTTCCGCT[A/G]GGCTCTGTCAGTCTG	55764
rs572422805	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506897	CGAGAGATGGCTTTA[C/T]AGTAACACACTCCAG	55764
rs572438935	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478321	CTGGTCACTAGAAAA[C/T]AAGTCTGTTCCATCA	55764
rs572487374	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496010	GCCGATCATGCAGGA[C/T]GACATGGTGCCTGCC	55764
rs572551211	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129489707	AGCCGGGCATGGTGG[C/T]AGGCGCCTGTAGTCC	55764
rs572562760	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129445005	CCACATAGCATAATG[G/T]TTAAAACATGGGCTT	55764
rs572607922	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513988	TTGAGGGTGGCTCCC[C/T]AGGGAGTCTGGACCA	55764
rs572709117	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462213	ATGTGAAGCACTGGT[C/T]TGTGTGCTTACACTG	55764
rs572816712	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475638	GCCTGGGCAACAGAG[A/T]CAGACCCTTTTTCAA	55764
rs572830625	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129488068	AGTAGCCCAGTCATG[A/G]GAGAGGTGCAGGATG	55764
rs572836270	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482350	GCTTTCTGCTGGGCT[C/T]GCGCCATTCTTTCTC	55764
rs572837999	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488529	CTGACCTGGGCTTGT[A/G]TCTTAGCCACTTCCT	55764
rs572841305	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440959	TAAACCTGAGATCTC[A/G]TTTCTCTAAAACTGG	55764
rs572884858	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476200	GAAAAGGCTGGCCAG[C/G]TCTCCCTGTCTTCCC	55764
rs572897559	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129482604	CACCTCTAGCCCAGA[C/G]GTAACTCCATGTCAG	55764
rs572928712	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129511158	GTCCTTCCTGGATAC[A/T]TGGCATCTTTCCCAG	55764
rs572948331	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129468706	GGCAAGGGAGTTTCT[C/G]CTGTGTGCTGGTCCT	55764
rs572957866	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439914	ATGTGAAACCTCTTC[A/G]GCTCACGGCACCGGG	55764
rs572999423	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469241	ACAACATTTGGCAAC[C/T]TGAGGCCAGGACTTC	55764
rs573002991	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504783	TTTTGCAGATGAGAA[A/C]ACTGAAGGGTAAAGA	55764
rs573046956	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129460286	GTTTGACTGCTTTAC[A/G]TACCTCATATAAGTA	55764
rs573102863	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129505375	ACATTGCAGAACAAA[C/T]GTCTCCCTGTTGGAG	55764
rs573119755	snp	A/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457428	CCCTCCGTTCCATGA[A/T]GACTCCGCTCATTCC	55764
rs573147299	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474431	AAAACTCCAGTGGTA[A/G]TAAGGAACTTGGGCT	55764
rs573165220	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129506133	ACTCTTAGACTTTGC[C/G]CTGGAATTTGGCCCC	55764
rs573185395	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500587	AGAATTCTTATGGGA[A/G]GAACCATGGATATCT	55764
rs573243054	snp	A/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129447617	TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	55764
rs573249927	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129443021	TGTATTCCAATCAGG[C/T]TAGCATCTGCTGTAA	55764
rs573317469	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129500841	GCTTAGATTTGCCAA[C/T]AGTGAGTGACCACCT	55764
rs573333751	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129518704	GGCGGTTTCCAGGGA[C/T]CTCCAGGTGAGTCTG	55764
rs573343465	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129460733	GAAGGAATGAATGAA[C/T]GAGTGAAGTTGTAAG	55764
rs573344156	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490578	CTAGCACAGCTGAGC[C/T]ACAGCTAGAAAGACC	55764
rs573382215	snp	C/G/T	5.35872e-05	0.00517598	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520215	TTGCTGGTGCTTCAG[C/G/T]ATGGCTGCTGCCCCT	55764
rs573416154	snp	A/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129446903	GTGTGTTTTGTTTTG[A/G]GTAACTTCAGTAGTA	55764
rs573492752	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129493530	TAAGGCTCAGCAAGA[C/T]GATGCCACATCCCCA	55764
rs573538818	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483266	ATACTTGCTTACTCA[A/G]AAATTCCAACAACAC	55764
rs573551653	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449131	TCACTATCTGGCTAA[A/G]TAATTTCTTTCTAGC	55764
rs573614979	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513060	AGCAAGGCATGTGGG[A/G]GAGGGTGAGGGGACC	55764
rs573650737	snp	C/T	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129513384	GAAGACCCAGAGCTC[C/T]TTGTTGTAAGAATTG	55764
rs573703099	snp	A/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129477001	CTCCTTGAGGATCTC[A/G]TGAAAGCAATAAATC	55764
rs573782501	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129462083	TACTCACTGTGTCTC[A/G]CTGATACGGTTCTGG	55764
rs573790388	snp	C/G	3.38352e-05	0.00411296	intron-variant	IFT122	GRCh38.p7	3:129463674	CCTTCATCTTCCACA[C/G]AGACTCTCAAAATCC	55764
rs573791382	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129499331	TGCTGGTGACTCAGA[A/G]AGGGCATGGAGGGCA	55764
rs573802090	snp	C/G	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129499791	CCCTGCCTACCTCCT[C/G]GTTGCCTGCTTCAGC	55764
rs573847501	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129500787	GTTGGGGGAAGTGGG[C/T]TGGCCACACTGGAAG	55764
rs573852615	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456857	GGAGTCGGAGGTTGC[A/G]GTGAGCCGAGATCGT	55764
rs573920497	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504852	GGCAGGGAGGTAATG[G/T]GAGCCAGGGTACCAT	55764
rs573960492	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461368	GCTAAAAATGCTAAA[A/G]TGCATTCAGAATATG	55764
rs574026636	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496127	TTAGCGCAGCATGCC[C/T]CACGCCTGCCGGCTG	55764
rs574113189	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453441	GTGTAGTGAGATCCC[C/T]GGTGACATGAAGGGC	55764
rs574125081	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445856	TCTGGAATAAGAGTT[C/G]GAAGTACTGTCATTG	55764
rs574149127	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129488141	TGGCGGCTGCAGGGC[C/T]GCTCCCCAGGCATGG	55764
rs574162184	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129446590	GCTAGAAGCCCCCTG[C/G]TTCAAGTTGTTCCAT	55764
rs574206622	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440649	GCTGCCTTGGATTCA[G/T]CTCACACCCACGAGA	55764
rs574213455	in-del	-/TTTTG	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129459283	GATACTGCATCTATT[-/TTTTG]TTTTGTTTTGTTTTG	55764
rs574233892	snp	A/G	0.00636936	0.0560724	intron-variant	IFT122	GRCh38.p7	3:129488602	CTCTATAGACGTAGG[A/G]TGATGACAGGCCCCA	55764
rs574238625	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129481094	TTAAACCAGGGATAT[C/T]AGTAAATGATAGCTA	55764
rs574267845	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129451112	GGGTTTTATTTTATT[C/T]CTTAGAGACAGGGTT	55764
rs574268503	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129455291	GATTCTCCTGCCTCA[G/T]CCTCCTGAGTAGCTG	55764
rs574276430	snp	C/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129447657	AGCTGGGATTACAGG[C/T]GCCCGCCACCACACC	55764
rs574278239	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441461	CACTCTCTAAGGTAG[A/G]TACTATAATTTCCTC	55764
rs574313179	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129448338	ACCTCTGTGGTGAAA[C/T]GCAGGTTTTATAGAT	55764
rs574315871	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474639	GTGTGGAGTGTAGCA[A/C]CTGTGAGGATGTGGA	55764
rs574343635	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129492450	TTGGGTTTCTAGTCT[A/G]TGAAAAGGGATTGGA	55764
rs574351765	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449184	CCTTCGAATCCTGTT[C/T]TCATGTGTCTCTTAA	55764
rs574428818	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475343	CTAAAAAAGGTTCAA[C/T]GTAGAGTTTAAAAAT	55764
rs574431438	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456808	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	55764
rs574440035	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439161	GTTTTCTGATGTAAT[C/T]TGGGGTAAAATAATT	55764
rs574448772	in-del	-/TGTCAGACCGT	0.00199481	0.0315187	downstream-variant-500B	IFT122	GRCh38.p7	3:129520554	TGGAGTCCGCCGATC[-/TGTCAGACCGT]TAGCATGTACATTTT	55764
rs574456392	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129487004	TTGCTCTGAGAGTAG[A/G]CAGACTCAAAATAAA	55764
rs574586658	snp	A/G	0.000875769	0.0209074	intron-variant	IFT122	GRCh38.p7	3:129488163	CAGGCATGGGTAATC[A/G]TCCCACGCATCTGGA	55764
rs574651202	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129511946	GAGTAGTTCAGAGAA[A/G]TGGAATAATTACCAA	55764
rs574693511	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129482269	TGGAGTCATCCAGCC[C/G]TGTGGCCTGAGGAAG	55764
rs574718623	snp	A/G	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129516912	AGACACACAGAGACC[A/G]CTCCTGCACACACAC	55764
rs574745616	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452141	TGCTAAGACTTCAGT[G/T]TGGTCATTCAATCTA	55764
rs574780336	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129508087	GGCCCTCTCCTTCAG[C/T]AGGGCGAAGGCCCAG	55764
rs574781623	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129515157	GCCAGTATAGTCCAC[A/G]TGCTCCGCACGGTGC	55764
rs574830091	snp	C/T	5.93431e-05	0.00544684	synonymous-codon	IFT122	GRCh38.p7	3:129515535	CAACAACCCGCTGCT[C/T]AACAACCTGGGCAAC	55764
rs574851376	in-del	-/AT	0.00517822	0.0506191	intron-variant	IFT122	GRCh38.p7	3:129442372	GTAATAAAATACTAG[-/AT]ATATATATAAAACGA	55764
rs574919568	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129440072	CCCCCACACGCCCCG[A/G]CCAATCGCTCGCGCT	55764
rs574941223	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129466755	CGATTCACTTGCCTC[A/G]GCCTCCTGAAGTGCT	55764
rs574956876	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440455	GCGTGTTTGAGGGGG[A/G]CAGCGGGCTTGCTGC	55764
rs574964006	snp	C/T	0.00398564	0.0444627	intron-variant	IFT122	GRCh38.p7	3:129510217	AGGCATGAGCCACCA[C/T]GCCCAGCCTTCCCGC	55764
rs575004134	snp	A/G	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129459529	CTCCTGACTACATCT[A/G]TTTTTTTTTTCTCAC	55764
rs575117014	snp	A/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129502974	TTGGGGTTCAGATGG[A/G]GAGAAGCTGCCCTCG	55764
rs575161540	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129468667	CTTGAACTAGATTCC[C/T]AGGTAGCTTGCTCTC	55764
rs575161593	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129461525	TCAGAGACTACAGGA[A/G]GGGCCCCAGCAAAGG	55764
rs575204772	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497858	GAAAATTGCTTCCCA[A/G]GATTCAATCTGGTTT	55764
rs575214156	snp	C/T	0.000159009	0.00891512	missense	IFT122	GRCh38.p7	3:129481593	CAGGCCACAGCTGTG[C/T]GCTGCTTGGACATGA	55764
rs575266427	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129487663	GGAAGAAGAGGCCAT[C/T]CCAGACCGCTTCCTC	55764
rs575269961	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472231	GATCATGGTTCACTG[C/T]AGCCTTGATCCCCCT	55764
rs575271648	snp	C/G	0.0123036	0.0774623	intron-variant	IFT122	GRCh38.p7	3:129516157	CTGCACACACACACA[C/G]AGACCGCCCCTGCAC	55764
rs575334954	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475496	GTCTCTGCAAAAAAT[A/G]CAAAAATTAGCCAGG	55764
rs575344646	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129511072	TGGAGGTGAGTGGTA[A/G]TTTGTGGTTCAGCAT	55764
rs575492979	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129504935	AATAGAAACTCAGCT[C/T]CTATTTCTGGCTCAG	55764
rs575512764	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129464920	TCCCATTTGTATGGA[-/T]TTTTTTTTTTAATAG	55764
rs575543198	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129463454	CATTCAGCATAAAAT[C/T]CTGGAGATCCATCTA	55764
rs575546988	snp	A/G	0.00119737	0.0244387	intron-variant	IFT122	GRCh38.p7	3:129518072	GCGCTCAGTCTGGTC[A/G]GTCACAGGCTGGCTC	55764
rs575547054	snp	A/T	0.00159617	0.0282053	intron-variant	IFT122	GRCh38.p7	3:129512136	CACAAGGTTATTATG[A/T]TAAAGACCAGATGAG	55764
rs575631795	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465277	AGTTTGGGCAGAATA[C/T]GTGCCCACCTGTTAA	55764
rs575703219	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503692	GGTGATGAGGTCAGT[A/C]ATGAGAAAAGGTGGG	55764
rs575710036	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497292	AATAAAATGCCTGGC[C/G]TTGGTGCCCCAGAGC	55764
rs575732818	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476253	AAAAAGCCCTTAATT[A/G]TATTGCAATGGTTAT	55764
rs575759125	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129498457	AAGGCCCAAACTAGG[C/T]GGGGACAGCGGCTGC	55764
rs575773715	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129497757	CCCCCACCTGGTAGT[C/G]TGAATTTGAGAAATA	55764
rs575822569	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129453510	AGTTGGTGTGATTGT[A/G]TCTTTTTCTCCAGCG	55764
rs575833013	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129452959	GACAGATTGGATATG[G/T]GCTATGAAGAAAAAG	55764
rs575883839	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493875	TGTAGTCCTCTCCTC[A/G]TATGCTATGAGCTGG	55764
rs575884458	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129467443	TGTGAACCCTTTCCA[A/G]TAACATTACAAATCC	55764
rs575949203	snp	C/G	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129449453	TAGTAATTTCCCTGA[C/G]GGGAGGGAGGGATTA	55764
rs575955834	snp	A/G	5.28695e-05	0.0051412	intron-variant	IFT122	GRCh38.p7	3:129515645	GGACAGCCTGTGGAC[A/G]GCCAGGCTCACTCCA	55764
rs575984915	snp	A/G	0.00358779	0.0422022	intron-variant	IFT122	GRCh38.p7	3:129479467	TAAATAATCAAAGTT[A/G]GAACTCCAAGCGGTT	55764
rs576039379	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129451287	TTTTTTTTTATTTTT[A/T]TTTATTTTTATTTTT	55764
rs576050088	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129493043	GGCTGGTTTCAAATT[C/T]GTGGGCTCAAGCTAT	55764
rs576055227	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503492	TGGCTCAACCCCCAC[C/T]CTCCAGCTCACTGGC	55764
rs576146692	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129451799	AGTTTTTATTGGCTA[C/T]AGATTTAGAATATTG	55764
rs576189260	in-del	-/AGAAG	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129443935	AAATGACCCTTATGA[-/AGAAG]AGGTCACACAGGAAT	55764
rs576252158	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129471156	CAGTGAAGCCTTTAA[C/T]TGCGTAGCATCCTTA	55764
rs576292855	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129444224	TTCCGCCATGCTGCT[A/T]CTCAAAATGTGAAAT	55764
rs576309283	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453263	ATGTGGTAGTAGGAA[C/T]CTAATGGAAATTCTC	55764
rs576312489	snp	C/T	0	0	intron-variant	IFT122	GRCh38.p7	3:129480121	CCCTCACACTCCTAG[C/T]AGGCCCACGTTTTGG	55764
rs576332329	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444795	AAAATGCTAAGATTA[C/T]AGGCGTGAGCCACCA	55764
rs576374850	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484027	GGAGTCCGGCAGGGT[A/G]TGTGTGTGAGTACGT	55764
rs576408529	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129459052	CAGGCCTCCTCTTAC[A/T]ATTGGGGATCTGCCG	55764
rs576461433	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496651	GTGATGTTGCCCAGG[A/G]CCTATTGTTCATCAG	55764
rs576509644	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484699	TATGAAGTGCTGGCT[A/G]TACACTAGTCATCTG	55764
rs576522383	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129490425	TGAGCAGAGCTGCAG[G/T]TTCCTCCCTATTCCC	55764
rs576540254	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129478523	GCAGTGGCACAATTA[C/T]GGCTCACTGCAGCTT	55764
rs576577674	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486325	CTGTAACTAGAGCAA[C/T]TCATTTCACTCTTTG	55764
rs576581772	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129486956	GGAGAGATGGCATGG[C/T]GGAAAAGATAAGCAC	55764
rs576584569	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129479196	GGAGGCCAAGGCAGG[A/G]TGATTGCTTGAGGCT	55764
rs576667525	snp	C/G	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129501979	GGAGAGTTAGTTTGA[C/G]TCCAAATTCCAGCCT	55764
rs576682689	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129508741	TGTGGAAGCATTTTC[C/T]CTGCAAAAAGTTGTT	55764
rs576700258	snp	A/C	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129464521	ATGAAACCATATCCC[A/C]GCTGTTGCTGCCTCA	55764
rs576740776	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129510406	TTCCCACAGCAGGGT[C/T]AGTGGTCTCAAGGGA	55764
rs576743578	snp	A/C/G	3.30859e-05	0.00406719	missense	IFT122	GRCh38.p7	3:129514529	GTACCCTGACCATCC[A/C/G]CGCCAAGCCCTTCCA	55764
rs576753615	snp	A/G	0.000112496	0.00749904	intron-variant	IFT122	GRCh38.p7	3:129481514	ACTGACACTGTTTTC[A/G]CTGAAATTTTGCCAG	55764
rs576805711	snp	C/G/T	6.58907e-05	0.00573948	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451942	CTGATGGCACCTTAC[C/G/T]TCAGCCCCTCAAGGG	55764
rs576839699	snp	C/T	0.00318978	0.0398085	intron-variant	IFT122	GRCh38.p7	3:129498312	GAAGGACATTTCTAG[C/T]CTCCTAAGATGCCTG	55764
rs576842011	snp	G/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129444886	TTATTAAAGGAAGCG[G/T]CAGGTCAACAGAGCC	55764
rs576858156	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129491973	GATAAAGCCATGCCT[C/T]GCTGGGTGGTATAAC	55764
rs576875617	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129445788	TTCCTACCTCACAGA[A/G]TTATTGTGGAGATGA	55764
rs576896156	in-del	-/CA	0.0418186	0.138422	intron-variant	IFT122	GRCh38.p7	3:129517218	CACAGACTGCCCCTG[-/CA]CACACACACACACAC	55764
rs576904051	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129492395	GTGAGCTGTTGTGTG[A/G]TAGCTGGGTGAGGCA	55764
rs577018645	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129516341	CACACAGAGACTGCC[C/G]CTGCACACACACACA	55764
rs577027085	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129465376	TAAAGCCTAGAGATA[C/T]ACAAACAATTGGCAC	55764
rs577076331	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129516885	GCACACACACAGACC[A/G]CTCCTGCACACAGAC	55764
rs577097182	snp	C/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129473881	CTGCCTGCTTTTGGT[C/T]GCCCTGAAATGGTTG	55764
rs577123479	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457017	AAGGCATTGAGGCTC[A/G]GAGAACAGTGACTTG	55764
rs577206061	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520071	TGTGTCCAGCCCTGA[C/G]CACTGCCAAGCCCCC	55764
rs577218215	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129444109	CTGGCTTGTGCACCC[C/T]GTGAGTAGGAGGCTA	55764
rs577219103	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	IFT122	GRCh38.p7	3:129520554	TGGAGTCCGCCGATC[C/T]GTCAGACCGTTAGCA	55764
rs577254266	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129513947	TGCAGACAGAGTGGG[G/T]TACACCCAGGGGCCT	55764
rs577255585	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129463989	GAATCCAGAATCTCT[C/G]ATTGACAGGCCATGT	55764
rs577261551	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129484829	ATAAATTGTAGGAAA[C/T]AATACAGAGATCCCT	55764
rs577292702	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129491120	CTCAGTCTCTTGACA[C/G]GAAGCCTGGTCCTGT	55764
rs577318057	snp	C/T	0.000399281	0.0141238	intron-variant, missense	IFT122	GRCh38.p7	3:129506774	GTTGGCAGGTCCAGC[C/T]CTGCATTGCTAATTC	55764
rs577362345	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472001	AAATTGAAGCACAGA[C/G]AGGCTCAATAATTTG	55764
rs577371133	snp	A/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129472767	CTGTTATTATTTTTT[A/T]AAATCCCTTCTTTTC	55764
rs577376107	in-del	-/CA	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129501203	AGGCTCAAGCATGTG[-/CA]CACACACGTGCACAT	55764
rs577418383	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129516111	CTGCACACACACACA[C/G]AGACTGCCCCTGCAC	55764
rs577528463	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518791	GCAGACCCCCAGCAG[C/T]CACTGAATGTTTCTC	55764
rs577539049	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509031	AGTGATCATGACCTT[G/T]TTTTGGTGCAAGTTT	55764
rs577575087	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129501993	ACTCCAAATTCCAGC[C/G]TGACCAGAGAGAACA	55764
rs577578618	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129496138	TGCCTCACGCCTGCC[A/G]GCTGCAGAGTGGCTA	55764
rs577601144	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129509551	ACTCAAATAAGAAAA[C/T]TGCTTGAATTTGTTT	55764
rs577611342	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129502534	GTAAAGGCCACCTCT[A/C]CCAGATCCTGGTGAT	55764
rs577648631	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454621	AGGGAGCCTGGAGAG[C/T]TGAACTGTTTCTGTC	55764
rs577694615	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129494778	CTGGAGTCAGACAGA[A/G]CTGCGTCCAAATTCC	55764
rs577705338	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129469488	TGAGATTCTGTTACT[A/G]TTAATTATACATTAT	55764
rs577740740	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456888	GCCACTGCACTATAG[C/T]CTGGGCAACAGAGTG	55764
rs577747243	snp	A/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129462808	AGGCACTGAGCCAGG[A/G]CATCTGGGACAGGGG	55764
rs577753735	snp	A/T	0.000798403	0.0199641	intron-variant	IFT122	GRCh38.p7	3:129488724	CTGTTCTCTGTGGGA[A/T]GCACCTGACTAGTAG	55764
rs577766324	snp	C/G	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129489114	TCCCTCTTTATCTCC[C/G]CACAGTCAATTAATG	55764
rs577776131	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129463795	GGGAAAGACTTGTGC[C/T]TTTGATCATGAAGCA	55764
rs577797227	snp	A/C	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129449819	TTCCTGGCCATTAGC[A/C]GACTTCATCATTTTG	55764
rs577841017	snp	G/T	0.0182019	0.0936463	intron-variant	IFT122	GRCh38.p7	3:129450715	TGTGTGTGTGTGTGT[G/T]TTTTTTTTTTTTTTT	55764
rs577844756	snp	C/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129496725	GTGATTTCTTCACTC[C/T]GTACCTGAGACCCAG	55764
rs577890215	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129464455	TGTTTATTACAGAAC[G/T]AAATAGCATTTTAAG	55764
rs577923581	snp	A/G	1.6501e-05	0.00287232	intron-variant	IFT122	GRCh38.p7	3:129499887	AGAGTGTTTTTGTTT[A/G]TTGTGCTTCCTCAGG	55764
rs578028417	snp	C/T	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129490474	CTCATTCAGGGGCCT[C/T]GTGACTCTGACCAGG	55764
rs578057938	snp	A/G	0.00279162	0.0372561	intron-variant	IFT122	GRCh38.p7	3:129449010	GGCCTCAGCTTGCCT[A/G]TCTATGTTTGCAGCT	55764
rs578102788	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487317	GCGTGCATACATGTG[A/G]CAGGAAGGGGCACAG	55764
rs578119180	snp	G/T	0.000399281	0.0141238	intron-variant	IFT122	GRCh38.p7	3:129483349	TCTTTGTGGTCCCCT[G/T]TCATCCTTTTCCCTC	55764
rs578148039	snp	C/T	0.0023933	0.0345097	intron-variant	IFT122	GRCh38.p7	3:129518734	GACCCGCCCTGGGGT[C/T]AGCAGGGACTCTCGC	55764
rs578217789	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448369	AAGCTTGAGGAGGTG[A/G]TGTCTGATTTACATA	55764
rs578233160	in-del	-/A	0.00478085	0.0486577	intron-variant	IFT122	GRCh38.p7	3:129487738	CTGAGGGAGGCCGAT[-/A]ACAACCCACCACTGC	55764
rs745308803	snp	A/G	3.33973e-05	0.00408626	missense	IFT122	GRCh38.p7	3:129483668	TTCTCCATTTCTGCC[A/G]TGGAGGTGCCGCAGG	55764
rs745315648	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517220	CAGACTGCCCCTGCA[-/CA]CACACACACACACAG	55764
rs745364806	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438782	AAAAACAAAAAAAAA[C/T]AAGCAACCGGGCGTG	55764
rs745406757	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485715	CTCTCTGACTGTGGC[C/T]GGCCAAGAGGAGCCA	55764
rs745407950	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129471745	AGGAAGATTTAGAAT[G/T]CAATATAGGATGATG	55764
rs745440924	in-del	-/TT	1.64738e-05	0.00286995	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476415	ACAAGCAAGTATCTC[-/TT]TTCACCAAGGATGGA	55764
rs745481731	in-del	-/T	3.29649e-05	0.00405973	intron-variant	IFT122	GRCh38.p7	3:129488229	CTGAAAACAGTCTTC[-/T]TTTTTTTCCCTTGAT	55764
rs745484070	snp	G/T	4.94572e-05	0.00497254	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478174	ATCAAGAAGTTTGAG[G/T]GCAACCTCCTGGTGG	55764
rs745493118	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472959	TTTATTCATTACAAG[C/T]GTATTTTTCTTTATA	55764
rs745512203	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129496948	TAGGGTTGGGAACCC[C/G]TGAGGCCTCCTCAAG	55764
rs745537565	snp	A/G	1.70519e-05	0.00291987	intron-variant	IFT122	GRCh38.p7	3:129488177	CATCCCACGCATCTG[A/G]AGGCAGGCTCTGTAT	55764
rs745564592	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129510873	AAAACGTTGTCCCTG[A/C]AGTCAGTCCCAGTCT	55764
rs745565781	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516247	GACTGCCCCTGCGTG[-/CA]CACACAGACTGCCCC	55764
rs745578992	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473946	CTTTGTGGGAAGATT[A/G]GTCCGATGGGAACTA	55764
rs745581144	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457121	TTACCTCTTAATCCT[C/T]GTCTCTCACCAGAGT	55764
rs745626141	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506452	AGCGGTCCAGGTGCT[A/G]GAGCAGCTCACAAAC	55764
rs745626246	snp	C/T	1.64901e-05	0.00287137	synonymous-codon	IFT122	GRCh38.p7	3:129495493	CCTGTTTCTGGCAGA[C/T]GTGTTTTCCTACCAG	55764
rs745679313	snp	A/C	4.95054e-05	0.00497496	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504463	AGAAGGAGCAGGAGA[A/C]GTTACTGCCAAGACA	55764
rs745679505	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129478290	GTGATAGGGTGCCCA[C/T]CTCATGGTTTTAAAA	55764
rs745692614	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129462866	CATGGGAGAGGCACA[A/G]CTCAGATAGAGTCAT	55764
rs745732271	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129446730	CAGGACCACCTGAGG[A/G]CTGTGTCATGGGCTG	55764
rs745753303	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129464073	TGACAGATAGGGATA[A/T]AAATACTGACTTGAC	55764
rs745762753	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449923	CTGATTTTGGCTGCC[A/G]GAAGCAGATTACTGG	55764
rs745790183	snp	A/G	1.65373e-05	0.00287548	missense	IFT122	GRCh38.p7	3:129481672	TGGTGTATGACATCG[A/G]CACCAAGGAGCTGCT	55764
rs745820316	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129508327	GTGATGGGTTGTCAA[A/C]AGCCTCTTCATCCAC	55764
rs745838437	in-del	-/GTGTGT			intron-variant	IFT122	GRCh38.p7	3:129465115	TGTACATGTATATGA[-/GTGTGT]GTGTGTGTGTGTGTG	55764
rs745849984	snp	C/G	1.64988e-05	0.00287213	intron-variant	IFT122	GRCh38.p7	3:129452020	GGCTGCTCTGGGTTT[C/G]CATTCTCTATAATAG	55764
rs745856685	snp	C/G	3.29533e-05	0.00405901	intron-variant	IFT122	GRCh38.p7	3:129519077	TCTCCATCTCTGCTT[C/G]TGATTCCATCCTTGA	55764
rs745857213	snp	A/G	1.64738e-05	0.00286995	missense	IFT122	GRCh38.p7	3:129495572	AACCTCGCGCTTGAA[A/G]TGTACACCGACCTCT	55764
rs745897332	snp	G/T	6.70084e-05	0.00578789	intron-variant	IFT122	GRCh38.p7	3:129514309	AGCTGTGTTCCAGCC[G/T]GGGGCTCACTCCAAG	55764
rs745973196	in-del	-/CTC			intron-variant	IFT122	GRCh38.p7	3:129495044	GAAACCCTAAACATT[-/CTC]CTGCTCTGTCATCCC	55764
rs746041263	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453365	TTCAGAGAGTTGAAG[A/G]GAAAGGGAAAAAGTG	55764
rs746069565	snp	C/G	5.05489e-05	0.00502711	intron-variant	IFT122	GRCh38.p7	3:129502906	AAAGCAGGCCTCATG[C/G]GCTGGGGCCCCACCT	55764
rs746075285	snp	C/T	1.65351e-05	0.00287528	intron-variant	IFT122	GRCh38.p7	3:129463539	CCAATCCATCTTCTT[C/T]TATATTATTGTGCAT	55764
rs746090651	snp	A/C	1.6473e-05	0.00286988	missense	IFT122	GRCh38.p7	3:129488300	GGAAACTGTTCAAGG[A/C]AGCCTACCAGATTGC	55764
rs746117912	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469461	AGTCATGCCTGTTAT[A/G]TTTTCATTTTCTGAG	55764
rs746128672	in-del	-/GTA			intron-variant	IFT122	GRCh38.p7	3:129493861	TACTGGGGTCAAAAT[-/GTA]GTCCTCTCCTCGTAT	55764
rs746129224	snp	C/T	1.65449e-05	0.00287614	stop-gained	IFT122	GRCh38.p7	3:129514414	TTCACCTTGGCCAAG[C/T]AGAGCAAGGCCCTCG	55764
rs746132091	snp	C/T	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129476660	AGTTCTCTCACCCCG[C/T]AGGTGGTCGGCTGCC	55764
rs746134493	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441668	GAGACAGGCAGGTAA[C/G]ATAAATGGGAGATGT	55764
rs746135479	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508562	AGACTGAATTTTAAA[C/T]CATTATAACTAGGCT	55764
rs746155973	snp	A/C	1.65919e-05	0.00288022	intron-variant	IFT122	GRCh38.p7	3:129488415	AAGCATCTAGCCAGC[A/C]GGAGCTGGAGTTTGG	55764
rs746196323	snp	C/T	3.80923e-05	0.00436403	synonymous-codon	IFT122	GRCh38.p7	3:129515577	CTGCCGCCAGCCCTT[C/T]ATCTTCTCCGCCTCT	55764
rs746228498	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129478391	GGATGAACCAGACTC[-/T]TATCAGCAAGTCATG	55764
rs746236976	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458413	TTTGTTTACTCAGTG[C/T]CAGACAAAGCAGGTT	55764
rs746274228	in-del	-/AAAT			intron-variant	IFT122	GRCh38.p7	3:129509540	ACCCATTTTGAACTC[-/AAAT]AAGAAAACTGCTTGA	55764
rs746276677	snp	C/G	0.0149472	0.0851479	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440310	CGGGTAGGAGGAGCC[C/G]GAGCCGTAAGGGAAG	55764
rs746343325	snp	A/T	1.81995e-05	0.00301653	intron-variant	IFT122	GRCh38.p7	3:129467102	GGGAACCCTTCTGGT[A/T]AGGGCCCAGGCCCCA	55764
rs746380030	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129484240	AGAACCACAGACAGG[C/T]GCCTGAGATTGACCT	55764
rs746401252	snp	A/C	3.29451e-05	0.00405851	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449876	TTCTGTTCAGTATAA[A/C]TGACATCGCATTTAA	55764
rs746444429	snp	C/T	1.64781e-05	0.00287033	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507618	GGGGCCAGTTGGCAG[C/T]CACAGACACTGTTTG	55764
rs746446315	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482084	CTCACCTGCTGCAGG[C/T]CTGCCTGTGTCTATG	55764
rs746452983	snp	C/G	8.31096e-05	0.00644577	intron-variant	IFT122	GRCh38.p7	3:129517422	GCCTGGCGGCAAGTC[C/G]TTTGCAAGGCCTCCA	55764
rs746457079	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129467279	GGAAATACTGAAAAG[A/G]CTAAAGGAGAAAGTT	55764
rs746478905	snp	A/G	6.58903e-05	0.00573941	missense	IFT122	GRCh38.p7	3:129500001	AAAGCCGCCGTGGAG[A/G]TGTACATCTCAGCAG	55764
rs746495773	in-del	-/TCACAGAC	6.58913e-05	0.00573945	frameshift-variant	IFT122	GRCh38.p7	3:129488327	TTGCTTGCTTGGGTG[-/TCACAGAC]ACTGATTGGCGTGAA	55764
rs746544840	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129474025	AATTTTTAGTTTTCT[C/T]GTTAGGTTTTCTAGC	55764
rs746556063	in-del	-/AGA	1.64754e-05	0.00287009	cds-indel, downstream-variant-500B	IFT122	GRCh38.p7	3:129507677	CAGCAGATCCTGCCC[-/AGA]AGGACACAATGCTTG	55764
rs746580177	snp	C/G	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469363	ACGTAATGACATCCT[C/G]GCTGTGGCTGACTGG	55764
rs746661728	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493964	AGTGTGCTCTATATC[A/G]ACTGCCTGCAGACTT	55764
rs746672790	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460899	CCATCTTCCATTTCT[A/G]GGCCTCCACAAAACA	55764
rs746693194	snp	A/G	1.65337e-05	0.00287517	missense	IFT122	GRCh38.p7	3:129483572	CTCAACATCAAAGCC[A/G]GCACCTTCCCTGTGC	55764
rs746712172	snp	A/T	3.29473e-05	0.00405864	missense	IFT122	GRCh38.p7	3:129500065	ACCATGGCTGGGTTG[A/T]CATGTAGGTTTTGGT	55764
rs746761833	snp	A/C	3.30562e-05	0.00406534	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478042	TGCAAAGAGCTTGTC[A/C]AGAAGATTGCCATCT	55764
rs746788932	in-del	-/ACACACAG			intron-variant	IFT122	GRCh38.p7	3:129517296	CACACACACACACAC[-/ACACACAG]AGACTGCTCCTGCAC	55764
rs746817333	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509648	AAAGCGAGAAATGCC[C/T]GTTGAAATGATGTAT	55764
rs746863945	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129451139	GGTTGTGCTCTGTTG[C/G]CCAAGCTGGTGTGCA	55764
rs746890917	snp	A/G	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129517562	TGCTGAGACCCAAGC[A/G]GGATGACAGACAGCT	55764
rs746907219	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508690	TACTTTGGGATTTGA[C/T]GAACTCTTGGAAAGC	55764
rs746907640	snp	C/G	1.64757e-05	0.00287012	intron-variant	IFT122	GRCh38.p7	3:129466876	AATTTTGAACAACTA[C/G]TTACTGTCTACAGCC	55764
rs746908011	snp	C/T	1.65353e-05	0.00287531	missense	IFT122	GRCh38.p7	3:129495468	AGAAGCGGGGAGAGA[C/T]CAACAATGACCTGTT	55764
rs746924794	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485862	ACACATTCTCAAGAC[A/G]AAGGCTGTTCATCTG	55764
rs746925366	snp	A/C			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438955	AAACCCACTAAACTA[A/C]AACTTCATTAAAGTT	55764
rs746935814	snp	A/G	1.64749e-05	0.00287005	intron-variant	IFT122	GRCh38.p7	3:129451894	TCACATAGATAATCT[A/G]TATTTGTCTCTTTTG	55764
rs746968735	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464744	CGGCCGGGGGGCTCC[C/T]TCTCGCCAATATGGT	55764
rs746980150	snp	C/T			downstream-variant-500B	IFT122	GRCh38.p7	3:129520517	CTTTCAGAACGGCTC[C/T]GAGTTGTTCGTGGCA	55764
rs746987326	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473104	CCAGGAGTTCAAGAC[C/T]AGCCTGGGCTACATA	55764
rs747022888	snp	C/T	3.60985e-05	0.00424829	synonymous-codon	IFT122	GRCh38.p7	3:129481572	TTTGCTATCGTCCTG[C/T]TGAAGCAGGCCACAG	55764
rs747032492	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129450713	GTGTGTGTGTGTGTG[-/T]TTTTTTTTTTTTTTT	55764
rs747048238	snp	A/G	4.94205e-05	0.0049707	synonymous-codon	IFT122	GRCh38.p7	3:129495565	GCACGAGAACCTCGC[A/G]CTTGAAATGTACACC	55764
rs747061523	in-del	-/TG	0.000158743	0.00890765	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440417	AGGTCGAGTCCTCGC[-/TG]GGGGAGTGCGCGAGC	55764
rs747062791	snp	C/T	1.64768e-05	0.00287021	intron-variant	IFT122	GRCh38.p7	3:129519062	GGAGGCTAGGGTCTG[C/T]CTCCATCTCTGCTTC	55764
rs747129730	snp	G/T	1.64879e-05	0.00287118	intron-variant	IFT122	GRCh38.p7	3:129452011	ATGGTAAAAGGCTGC[G/T]CTGGGTTTCCATTCT	55764
rs747149221	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129442798	TTCCATGTCAAGTCG[C/T]GCATTTTGCTAGAGG	55764
rs747211414	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490289	TCTAAATCCCGAGTA[C/T]CCCACCTCTTTACTC	55764
rs747238423	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129446390	CCATCATGCTTGGCT[-/A]ATTTTTTGTAGAGAC	55764
rs747257777	snp	A/C	1.65466e-05	0.00287628	missense	IFT122	GRCh38.p7	3:129481667	TTGCCTGGTGTATGA[A/C]ATCGACACCAAGGAG	55764
rs747259787	snp	A/G	3.2993e-05	0.00406145	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476336	AAGGATCGGGCACTG[A/G]ACTTTGACCCCTGCT	55764
rs747273489	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129494506	CTTTCACCAGCTTGT[C/G]TAAGAGTTTGATTCA	55764
rs747295684	snp	C/T	3.29478e-05	0.00405867	missense	IFT122	GRCh38.p7	3:129512397	CCAAGGACACCCCCT[C/T]GGGCATCTCTAAAGT	55764
rs747305545	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129454515	TGGTAGTCATATTTG[-/TG]TGTGTGTGTGTGTGT	55764
rs747336013	snp	A/C/T	4.94534e-05	0.00497239	missense	IFT122	GRCh38.p7	3:129502815	GCTATGCTGCTGAGA[A/C/T]CTACCTGAAGATGGG	55764
rs747336156	snp	C/T	0.000198636	0.00996386	intron-variant	IFT122	GRCh38.p7	3:129488206	ATGCATCTGGTTCTT[C/T]CCATGGCTCTGAAAA	55764
rs747349090	snp	C/G	0.000335683	0.012951	intron-variant	IFT122	GRCh38.p7	3:129514290	CCTTCCCGGCACCAG[C/G]ACAAGCTGTGTTCCA	55764
rs747378741	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448274	TAACAGGCGAAAGAA[A/G]GAGAAGAGCTCACTG	55764
rs747402680	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486682	AGAGCCTGGGAGATG[A/G]TGAGGAGCTGGTGCT	55764
rs747428443	snp	C/T			missense	IFT122	GRCh38.p7	3:129506541	TGCAGTGCCTCGATA[C/T]AGCTCAAGGTGTGTA	55764
rs747461940	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517040	CACAGATTGCTCCTG[-/CA]CACACACACACACAC	55764
rs747486996	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129468503	ACACGCGACACCACG[C/G]CGAACTAATTTTGCA	55764
rs747491185	snp	G/T	0.000796813	0.0199442	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440299	AGACGCTGAGGCGGG[G/T]AGGAGGAGCCCGAGC	55764
rs747500385	in-del	-/CTC			intron-variant	IFT122	GRCh38.p7	3:129485532	GGGCACGAACAGCTT[-/CTC]CTGGACTGTGTCCTC	55764
rs747502364	snp	G/T	2.24792e-05	0.00335248	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439818	GACTCAGACTCTCCA[G/T]CCCAGTCGTGCCCAT	55764
rs747522117	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129483049	AGCCCTGCCAGGAGA[C/G]ATCAGCATTCCCAGC	55764
rs747527267	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129518350	TGGGAGGGGCTTCTG[G/T]CAGGGAACAGCACAC	55764
rs747550814	snp	A/G	3.29489e-05	0.00405874	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479796	CTAGGAGAAACGGCT[A/G]CAGTGCCTGTCCTTC	55764
rs747557748	snp	A/G	4.94214e-05	0.00497074	missense	IFT122	GRCh38.p7	3:129479872	TACATCAAGGTGATC[A/G]GTGGCCCTCCTGGAA	55764
rs747567404	snp	C/G	1.64732e-05	0.0028699	missense	IFT122	GRCh38.p7	3:129488264	TCCTGCAGTCCGCTC[C/G]CATGTACCAGTACCT	55764
rs747578684	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469494	TCTGTTACTATTAAT[C/T]ATACATTATCATTGT	55764
rs747581544	snp	A/G	1.6607e-05	0.00288153	intron-variant	IFT122	GRCh38.p7	3:129463527	GTAGTATTCCAACCA[A/G]TCCATCTTCTTTTAT	55764
rs747587003	snp	C/T	3.42097e-05	0.00413566	intron-variant	IFT122	GRCh38.p7	3:129515472	GGCCCCTCGGGAGTC[C/T]GTGGCTGTTTTGTAG	55764
rs747626363	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440893	AAAACTTAAAGTAGG[A/G]AGAAACAAAACTGAA	55764
rs747642457	snp	A/C/G	4.94249e-05	0.00497096	intron-variant, missense	IFT122	GRCh38.p7	3:129467005	GTGTACAGTAGTCAG[A/C/G]GTAGTGAGGCAGAGG	55764
rs747703549	snp	A/C			synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460950	TAAAGCACCTAAAGG[A/C]CAAGGTGGGAGGATT	55764
rs747843863	snp	A/C	1.64751e-05	0.00287007	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507674	ACACAGCAGATCCTG[A/C]CCAGAAGGACACAAT	55764
rs747849239	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129454514	CATGGTAGTCATATT[-/TG]TGTGTGTGTGTGTGT	55764
rs747889950	snp	C/T	1.65004e-05	0.00287227	missense	IFT122	GRCh38.p7	3:129519662	AGCGATGGCCCCCAC[C/T]CCTGAGGTGGCAATA	55764
rs747895686	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129502629	ATAGTATCAACACTG[A/G]GGACCACAGAATGAA	55764
rs747907389	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452702	TTTGATTCTCAGTCA[A/G]AATGGAACTACTGAA	55764
rs747929259	snp	A/G	1.65299e-05	0.00287483	missense	IFT122	GRCh38.p7	3:129514429	CAGAGCAAGGCCCTC[A/G]GTGCCTACAGGCTGG	55764
rs747962421	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129490716	CCTCTTGGCCACTGT[A/G]CTGGGCTTTGCAGGG	55764
rs747981988	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440623	CTCTTCCCTCACGGT[C/T]TGGCCCTGTCGCTGC	55764
rs747985469	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486931	AAGGGAGCATTTAAT[A/G]TGCCAATGAGGAGAG	55764
rs747990836	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129491928	GCAACTGGGATGTCT[C/T]TGCTGTTCTTTACAT	55764
rs748019891	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504366	TAAGGATGACATCTA[C/T]ATGCCGTATGCTCAG	55764
rs748033586	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441473	TAGGTACTATAATTT[C/T]CTCTATTTTATGTAT	55764
rs748041680	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129510700	CAGCTGAGCTCTGCT[C/G]CAGGACCTACATGGG	55764
rs748049791	snp	A/G	3.32127e-05	0.00407495	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478019	TTTCTTTGACAGTTC[A/G]GATTAAATGCAAAGA	55764
rs748063045	in-del	-/C	1.64727e-05	0.00286986	frameshift-variant	IFT122	GRCh38.p7	3:129512317	TCACTGCAGGAAGAT[-/C]CCGTTCAGTGTCCAT	55764
rs748070252	snp	C/G/T	3.29453e-05	0.00405854	missense, synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464657	AATGATGGTCAGTAC[C/G/T]TGGCGCTGGGGATGT	55764
rs748073267	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129474152	AAATTGGTGTAAGGG[A/C]ATTAATTTAACTAAG	55764
rs748086687	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129493798	GAGCATAATTTTCCT[C/T]TCTACAAAAGTAACT	55764
rs748099324	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129459002	CCTTATATCCACCCA[G/T]TGTCAAATGTCAGAA	55764
rs748109314	snp	A/G	4.95921e-05	0.00497932	intron-variant	IFT122	GRCh38.p7	3:129476819	AAGAGGCAGGTCCAG[A/G]CCTTGGGAAGAGGGA	55764
rs748137931	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129509763	AGCCTGTGTTCCTAG[C/G]CTTTCCCTCCCTGTC	55764
rs748155669	snp	A/G	0.000104727	0.00723549	intron-variant	IFT122	GRCh38.p7	3:129502934	CCTGAGCCCTGGGAC[A/G]CAGGCGGGTGGGTAC	55764
rs748159186	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475992	GCAGAGGGAGGGGGG[C/T]CTTTGGGAACAAAAC	55764
rs748171353	snp	A/G	1.64727e-05	0.00286986	intron-variant	IFT122	GRCh38.p7	3:129492207	GAGGTAAAAGATGAA[A/G]CATTTTTCCTTCTCA	55764
rs748196480	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490431	GAGCTGCAGGTTCCT[C/T]CCTATTCCCAGGCTT	55764
rs748203508	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129491618	AGAATCTGTCTTTAT[A/G]CCCTCTCAGCTTTCC	55764
rs748223896	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449905	AAGCCTGATGGAACT[C/G]AACTGATTTTGGCTG	55764
rs748256943	in-del	-/TGTGTGTGTGTGTGTGTGT			intron-variant	IFT122	GRCh38.p7	3:129465140	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGT]GTGGTGTGTGAGTGA	55764
rs748269922	in-del	-/A/AA			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438751	TCTTTGCAAAAAATG[-/A/AA]AAAAAAAAAACCCAA	55764
rs748269932	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505376	CATTGCAGAACAAAT[A/G]TCTCCCTGTTGGAGC	55764
rs748272790	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464734	AAAGATCGAGCGGCC[A/G]GGGGGCTCCCTCTCG	55764
rs748334887	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129444799	TGCTAAGATTATAGG[C/T]GTGAGCCACCATGTC	55764
rs748347164	snp	C/T	3.65157e-05	0.00427276	synonymous-codon	IFT122	GRCh38.p7	3:129481565	CAATCTCTTTGCTAT[C/T]GTCCTGCTGAAGCAG	55764
rs748368024	snp	A/G	1.64746e-05	0.00287002	intron-variant	IFT122	GRCh38.p7	3:129469420	GAGTGGAAAACAGGT[A/G]TGTAGCCCTGTACAA	55764
rs748382222	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487150	GAGGTCCTGGCTGAT[C/T]TCTCTTCCCTGCCCA	55764
rs748402230	snp	A/G	3.29723e-05	0.00406018	intron-variant	IFT122	GRCh38.p7	3:129479974	TCTGCATGCACACGT[A/G]GGTGACCCGTCTAGC	55764
rs748413611	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129508723	TTTCTGCATCCTGCT[C/G]GTTGTGGAAGCATTT	55764
rs748418131	snp	G/T	3.29511e-05	0.00405887	intron-variant	IFT122	GRCh38.p7	3:129500100	GCCCCGAGAAGCATT[G/T]GGCAGCATGTCATCA	55764
rs748426747	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129517687	AGTCCCAGGGGATCG[C/T]GGGCCATGCTGAGCC	55764
rs748434200	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129464230	TCAGCATCTGTTGAG[C/T]ACCTTCTACAAAGCA	55764
rs748463285	in-del	-/TTA			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441840	ATTTTACTTTTAACT[-/TTA]TTATAAACGTACCTA	55764
rs748465216	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512197	AGGAGTAGGTGCTCA[A/G]TAATCAGAGCCGCTC	55764
rs748470858	snp	A/G	3.29468e-05	0.00405861	synonymous-codon	IFT122	GRCh38.p7	3:129512386	GCACAGCCTGCCCAA[A/G]GACACCCCCTCGGGC	55764
rs748472398	snp	A/T	1.64746e-05	0.00287002	missense	IFT122	GRCh38.p7	3:129517520	GGATCACTGATGAAG[A/T]AGCCATCTCCCTCAT	55764
rs748475770	snp	A/G	1.64773e-05	0.00287026	intron-variant	IFT122	GRCh38.p7	3:129519056	TAGGGTGGAGGCTAG[A/G]GTCTGTCTCCATCTC	55764
rs748491102	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459443	TATAGGCGCTCACCA[C/T]CATGCCAGGCTAATT	55764
rs748498126	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129462159	AATACATGGAGAAAG[A/G]CCTGTCATTTGTTTA	55764
rs748523897	snp	A/G	8.23635e-05	0.00641677	intron-variant	IFT122	GRCh38.p7	3:129512279	AGCAGCTCTTGAAGA[A/G]CTCAATCCCTGTTTG	55764
rs748564385	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129484022	AGCCGGGAGTCCGGC[A/C]GGGTGTGTGTGTGAG	55764
rs748577739	in-del	-/GTGT			intron-variant	IFT122	GRCh38.p7	3:129465117	TACATGTATATGAGT[-/GTGT]GTGTGTGTGTGTGTG	55764
rs748600997	in-del	-/G	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129449845	TTTTGGTTCCTAATT[-/G]TCTTTTTCCCTTGTC	55764
rs748604230	snp	C/T	2.74729e-05	0.00370617	intron-variant	IFT122	GRCh38.p7	3:129461036	CTACAAATAAGAAAA[C/T]AGTGGGTGAGGAGAA	55764
rs748629073	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129500763	GAGGGTGAAGGACAT[A/G]GGCTGTGGGTTGGGG	55764
rs748633632	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129455175	AGTTCATTAAGTTTT[A/T]TTTGTTTTTTTTTTT	55764
rs748665769	snp	G/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506891	GATGAACGAGAGATG[G/T]CTTTACAGTAACACA	55764
rs748685976	snp	G/T	1.64732e-05	0.0028699	intron-variant	IFT122	GRCh38.p7	3:129488253	CCTTGATGAAATCCT[G/T]CAGTCCGCTCCCATG	55764
rs748702276	snp	C/T	1.66674e-05	0.00288676	intron-variant	IFT122	GRCh38.p7	3:129515462	TGCCTGCCCCGGCCC[C/T]TCGGGAGTCCGTGGC	55764
rs748721420	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129456036	GGGTCAACTGTATGT[A/G]CACATGTACATACAC	55764
rs748723964	snp	A/C	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476445	GAGTGCGGCTTGGGA[A/C]TGTTGGGGAGCAGAA	55764
rs748725479	snp	A/G	0.000131067	0.00809423	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520136	GTAGGGCTGATGAGC[A/G]CTAGGGCTTCAGCCT	55764
rs748730829	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469936	GAGCCCCTGTGTGGT[A/G]TGGTATGTGACACAA	55764
rs748781211	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482112	ATGCGCACCTACAGC[A/G]TGGGAAGGAAACAGG	55764
rs748815145	snp	C/T	3.61579e-05	0.00425178	synonymous-codon, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520226	TCAGCATGGCTGCTG[C/T]CCCTACTGCCGCAGG	55764
rs748815491	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129449711	GCTGCTGTGGTGTGG[C/T]GGTTGAATGGAATTT	55764
rs748826692	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129483426	TTGGGCTGAAATGTG[G/T]GAGCGCTGACCAAGC	55764
rs748840145	snp	C/T	0.000348262	0.0131913	intron-variant	IFT122	GRCh38.p7	3:129514570	GTGAGGATGCAGCAC[C/T]CTTGGGCAGGTGGCT	55764
rs748855701	in-del	-/CTTA	1.64727e-05	0.00286986	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451937	CACCTCTGATGGCAC[-/CTTA]CTTCAGCCCCTCAAG	55764
rs748903301	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129450998	GTGCTGGGATTACAG[A/G]GGTGAGCCACCGCGC	55764
rs748916663	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484338	CCATAAAACAGAGAC[A/G]TGCATAGCGAGAAAC	55764
rs748920979	snp	G/T	4.94246e-05	0.0049709	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479787	GTTTGCTTCCTAGGA[G/T]AAACGGCTGCAGTGC	55764
rs748922587	snp	C/T	1.64743e-05	0.00287	missense	IFT122	GRCh38.p7	3:129495579	CGCTTGAAATGTACA[C/T]CGACCTCTGCATGTT	55764
rs748931179	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506476	CACAAACAATGCCGT[A/G]GCGGAGAGCAGGTTT	55764
rs748954774	snp	A/G	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129506540	ATGCAGTGCCTCGAT[A/G]TAGCTCAAGGTGTGT	55764
rs748956276	snp	G/T	1.64732e-05	0.0028699	intron-variant, missense	IFT122	GRCh38.p7	3:129466908	ATGGGAGAGTTTCTG[G/T]ATGAACAGAGAGAAT	55764
rs749004248	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471517	CCACACTGCAGTGGG[A/G]GGGAATGGGGTCTTG	55764
rs749012483	snp	A/T	1.65405e-05	0.00287576	intron-variant	IFT122	GRCh38.p7	3:129499855	TGATGTAACGCTGGC[A/T]CAGGAAGTTCTGATC	55764
rs749016460	snp	G/T	3.30398e-05	0.00406434	stop-gained	IFT122	GRCh38.p7	3:129481680	GACATCGACACCAAG[G/T]AGCTGCTTTTTCAGG	55764
rs749062786	in-del	-/C	1.6599e-05	0.00288084	frameshift-variant	IFT122	GRCh38.p7	3:129514403	GGAAAATACTCTTCA[-/C]CTTGGCCAAGCAGAG	55764
rs749092561	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129518645	GGGCCTCCCTGCAGG[A/T]CCCCTGCTGGCCTCT	55764
rs749132588	in-del	-/A			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457626	CAGGAGATGTTGACC[-/A]AAGGGTAGTTTCAGT	55764
rs749137520	snp	A/G/T	3.29594e-05	0.00405941	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458610	TTAGGCAAGCGCTTT[A/G/T]CTTCTGGATCAGCTG	55764
rs749146926	snp	A/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476669	ACCCCGCAGGTGGTC[A/G]GCTGCCAGGACGGCA	55764
rs749151257	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477407	TATCTGGATGTGCTG[A/G]CCTTAGTGCACTGCT	55764
rs749189354	snp	C/G	1.64781e-05	0.00287033	synonymous-codon	IFT122	GRCh38.p7	3:129483535	GTGTGAGGACATGCT[C/G]TGCTTCTCGGGAGGA	55764
rs749236291	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472712	CTCTAATTACACTTA[C/T]ATTAGACCTTTTGTT	55764
rs749242480	snp	A/T	8.24314e-05	0.00641942	intron-variant	IFT122	GRCh38.p7	3:129483458	CAGGGTGGTTCTCAC[A/T]GGATCCCCACTGTCC	55764
rs749298476	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129462615	GGAACACAGATAACA[A/T]GTGCACACGTCAAAA	55764
rs749300450	snp	C/T	3.14926e-05	0.00396804	intron-variant	IFT122	GRCh38.p7	3:129514341	ACAGGCAGTGCCAGC[C/T]CCTGGGCCTGGTGTT	55764
rs749312572	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129493455	AATGCTGTTCTAGAT[C/T]CTCACATTAACTGAA	55764
rs749337024	snp	A/C	1.69896e-05	0.00291454	intron-variant	IFT122	GRCh38.p7	3:129502916	TCATGGGCTGGGGCC[A/C]CACCTGAGCCCTGGG	55764
rs749379985	snp	C/G	6.595e-05	0.00574201	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129463571	GAAGGGTTGTGGTCT[C/G]CTGAACAGAAGTCTG	55764
rs749394736	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508429	GTATCAAGTCATTTC[C/T]TCCTTTCAACCACAC	55764
rs749396783	snp	A/C	6.61233e-05	0.00574955	missense	IFT122	GRCh38.p7	3:129514426	AAGCAGAGCAAGGCC[A/C]TCGGTGCCTACAGGC	55764
rs749425816	snp	C/T	1.64906e-05	0.00287142	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476783	GTCATTGTGCAGCAC[C/T]TGATCACTGAGCAGA	55764
rs749445788	snp	C/T			synonymous-codon	IFT122	GRCh38.p7	3:129488340	TGTCACAGACACTGA[C/T]TGGCGTGAACTGGCC	55764
rs749466359	snp	A/G	3.29457e-05	0.00405854	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449884	AGTATAAATGACATC[A/G]CATTTAAGCCTGATG	55764
rs749533612	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129463255	GTAGATTGCCATCAG[C/T]GTGACACAGAACTAA	55764
rs749557658	snp	A/T	1.64808e-05	0.00287057	intron-variant	IFT122	GRCh38.p7	3:129479970	ATAATCTGCATGCAC[A/T]CGTGGGTGACCCGTC	55764
rs749566983	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129452356	TAGTATGCTGGAAGG[A/T]GATAACTGTTATGGA	55764
rs749571432	snp	C/G	9.98452e-05	0.00706489	intron-variant	IFT122	GRCh38.p7	3:129488429	CAGGAGCTGGAGTTT[C/G]GTCCTTGTGGGGTCC	55764
rs749579713	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129468110	AAAGGTCATCTGCAG[C/G]CTCCCTCATTAACAT	55764
rs749601918	snp	G/T	3.29522e-05	0.00405894	synonymous-codon	IFT122	GRCh38.p7	3:129517512	GGAGGAAGGGATCAC[G/T]GATGAAGAAGCCATC	55764
rs749621414	snp	C/T			missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439800	CAGCTCCGCGGTCCC[C/T]CAGACTCAGACTCTC	55764
rs749623757	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129456386	GCTCATGCTTGTGAT[A/C]TCAGCACTTTGGGAA	55764
rs749643935	in-del	-/A	1.65007e-05	0.00287229	intron-variant	IFT122	GRCh38.p7	3:129469458	GCAGTCATGCCTGTT[-/A]ATATTTTCATTTTCT	55764
rs749653110	snp	A/C/G	6.64059e-05	0.00576187	intron-variant	IFT122	GRCh38.p7	3:129517431	CAAGTCCTTTGCAAG[A/C/G]CCTCCAGCCCCCTCA	55764
rs749656155	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441057	GTCTGAAAAAGAACT[A/G]AAGGGGAATGACTTT	55764
rs749657416	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129497820	TCTAGTCCTGATTAA[-/C]CGTGGCATATTTTTG	55764
rs749663249	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129472842	TTTCATTGACTCTTC[G/T]GCAACTTCCAATATT	55764
rs749670705	snp	C/T	8.50506e-05	0.00652059	intron-variant	IFT122	GRCh38.p7	3:129514383	CCTTAACCCTGTTCA[C/T]GGCAGGAAAATACTC	55764
rs749684678	snp	A/G	1.6477e-05	0.00287024	intron-variant	IFT122	GRCh38.p7	3:129451872	CAGGAATTCTGACTA[A/G]TAGATATCACATAGA	55764
rs749718959	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129452843	AAGCATCATCCAGAC[-/AG]AGGGGGTGATGGTGG	55764
rs749783712	snp	A/C	0.000181553	0.00952593	missense, intron-variant	IFT122	GRCh38.p7	3:129460924	AAAACAGTAAGAGTA[A/C]CAGCCACAGATAAAG	55764
rs749785449	snp	C/T	0.000559984	0.0167236	intron-variant	IFT122	GRCh38.p7	3:129500081	CATGTAGGTTTTGGT[C/T]CCTGCCCCGAGAAGC	55764
rs749802105	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505893	GACCTTGGGTGTGAC[A/G]CTTTACCTCCATTTT	55764
rs749823738	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469392	GGGGACAGAAAGTTT[C/T]CTTCTACCAGCTGAG	55764
rs749838163	snp	A/G	3.31757e-05	0.00407269	intron-variant	IFT122	GRCh38.p7	3:129507810	ACCATCTCCTGAGCT[A/G]GGGGTCCCGGGCATA	55764
rs749851233	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129514680	TAGGCTCTGTGCCCC[C/G]TGCTCAAGCCTGGCC	55764
rs749889272	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129486419	AAATTTCTATTATTA[A/T]TTCTCCTTATTACTG	55764
rs749904369	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129467740	TGGGGTAGCCAGGAT[A/G]TCTCAGTTTGGCAGT	55764
rs749994328	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452917	GACTCTGGATATAAT[A/G]GGAGGGTGGAGCCAA	55764
rs750010740	snp	C/T	6.62021e-05	0.00575297	missense	IFT122	GRCh38.p7	3:129502871	CACGTGGAGACCCAG[C/T]GCTGGGATGAGGTGA	55764
rs750014466	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129486541	TTTAAGAAAAGCTTT[C/T]AGGAGTTTGAGAAAG	55764
rs750028193	snp	G/T	0.000245228	0.0110704	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439753	ATTCGGCGGGTCTGG[G/T]ACTAGGCGCTCACTA	55764
rs750099570	snp	A/G	1.64743e-05	0.00287	intron-variant	IFT122	GRCh38.p7	3:129476531	GAAAGTTTGTTCTGT[A/G]GGGCCATGGCTTGAA	55764
rs750109572	snp	A/G	1.64827e-05	0.00287073	missense	IFT122	GRCh38.p7	3:129502790	TACCTCAAGAAGCTG[A/G]ACAGCCCTGGCTATG	55764
rs750150605	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487500	TAAGAAAGAGAAGTC[A/G]TTAGGAACTATTCAT	55764
rs750154715	snp	A/G	0.000339634	0.013027	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520216	TGCTGGTGCTTCAGC[A/G]TGGCTGCTGCCCCTA	55764
rs750155487	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129464150	GGACAGTACCTGGTG[C/T]ACAGTAGACACTCTA	55764
rs750202030	snp	A/G	1.65086e-05	0.00287298	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520308	TCTGCCCGCCTTGGG[A/G]TCTGCTGGGCTGTGA	55764
rs750235567	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492985	ACCCCGCCTGATTAA[C/T]TTTTTGTATATTTTT	55764
rs750237844	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457863	ACCTCAGCCTCCAGA[A/G]TAGCTGGGACTACAG	55764
rs750270933	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503391	ACTACTTCTCTCTGG[C/T]GTCAGGGGCTGTAAA	55764
rs750282577	snp	G/T	2.31062e-05	0.0033989	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439870	AACGAGCCCAGCGCC[G/T]CAACGCCCAGGGTGT	55764
rs750299501	snp	G/T	1.64795e-05	0.00287045	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479770	TTTCCATGCAGAGCT[G/T]GGTTTGCTTCCTAGG	55764
rs750301228	snp	A/G	6.58913e-05	0.00573945	missense	IFT122	GRCh38.p7	3:129488345	CAGACACTGATTGGC[A/G]TGAACTGGCCATGGA	55764
rs750309487	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501881	AGGCCTCCGTGCCTT[A/G]CCTGTCTCCAGACAG	55764
rs750318303	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129445951	AAATTCAGAGGCCCC[C/G]CAACCATCTGAATGG	55764
rs750323471	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129479617	GTGGGGAAGCCTTGC[A/G]TGGAGTCTTGGATTA	55764
rs750343242	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129478557	CCTCCCAAGCTCAAG[C/T]GGTCTTCCTCCTGAG	55764
rs750353936	snp	C/T	1.64803e-05	0.00287052	intron-variant	IFT122	GRCh38.p7	3:129495637	CCCAGGCCCAAGCTC[C/T]AGCTTGGAGCCCACT	55764
rs750405146	snp	C/T	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129506523	ATTACTGGATGCTGT[C/T]CATGCAGTGCCTCGA	55764
rs750415370	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129481369	AAGCCATTGCCCCCC[A/T]CCCCCCTCTTTCTTT	55764
rs750428434	snp	A/G	5.55314e-05	0.00526902	intron-variant	IFT122	GRCh38.p7	3:129515604	CTCTTCCTACGGTGA[A/G]TCCCTGCATCCTGAG	55764
rs750443931	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516101	CAGACTGCTCCTGCA[-/CA]CACACACACAGACTG	55764
rs750451568	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	IFT122	GRCh38.p7	3:129460858	CATGTTTCCAGATCT[C/T]GGTCTGTGATGTCTT	55764
rs750452403	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129514218	TGGGCCTTGCCATCC[A/G]AGAAGTACACTCACC	55764
rs750477155	snp	A/G	6.6235e-05	0.0057544	synonymous-codon	IFT122	GRCh38.p7	3:129519570	GCCCACCCTGCAGCA[A/G]GGTGGCTCAGAGTTC	55764
rs750489759	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129510175	AAGTGATCCTCCTGC[C/T]TGAGCCTCCCAGAGC	55764
rs750506005	snp	A/C	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129469337	TTTTATCTTCTGTTG[A/C]TTAGAGAGGAACGTA	55764
rs750543224	in-del	-/CAG	7.22569e-05	0.00601026	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439719	AGGCCCAAAAGGGGA[-/CAG]TAACTTACCGGAGGT	55764
rs750623588	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129469257	TGAGGCCAGGACTTC[A/C]TTGTTCCTGTTGTTT	55764
rs750632049	snp	A/G	0.000124612	0.00789242	synonymous-codon	IFT122	GRCh38.p7	3:129483604	CCGGCAGAAGCTGCA[A/G]GGCTTTGTGGTCGGC	55764
rs750636797	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483942	GATGGGAGGGGTATG[C/T]AGTGTTGTCAGCAGC	55764
rs750660601	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471025	GGGTGGATTAAAATA[C/T]AGAGAGCATGGTAGT	55764
rs750678663	in-del	-/TCT	1.64741e-05	0.00286998	cds-indel, intron-variant	IFT122	GRCh38.p7	3:129460887	TTCATTGCACCTCCA[-/TCT]TCCATTTCTGGGCCT	55764
rs750761979	in-del	-/GTCCATGCA	1.64727e-05	0.00286986	cds-indel	IFT122	GRCh38.p7	3:129506521	TTATTACTGGATGCT[-/GTCCATGCA]GTGCCTCGATATAGC	55764
rs750800833	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129518258	TGAAAGCCCCGGGGC[A/G]CAGCTCAGCCTGCCC	55764
rs750848733	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129476811	AGAAAGGTAAGAGGC[A/T]GGTCCAGACCTTGGG	55764
rs750851904	in-del	-/AGT	1.6528e-05	0.00287467	cds-indel	IFT122	GRCh38.p7	3:129519591	CTCAGAGTTCGTGCC[-/AGT]GGTGGTGAGCCGGCT	55764
rs750859310	snp	G/T	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129464587	CTAGTTTTACCTTCT[G/T]TGGGGTGCTTCCCCT	55764
rs750861012	snp	A/C	1.72442e-05	0.00293629	intron-variant	IFT122	GRCh38.p7	3:129495412	TCCTGCCCATGGCTG[A/C]AGAGGCCATTTCCTT	55764
rs750864260	snp	A/G	3.36067e-05	0.00409905	intron-variant	IFT122	GRCh38.p7	3:129477992	CAACCTCTTGCTAGA[A/G]CTAGATATTTTTTTC	55764
rs750869627	in-del	-/GGG			intron-variant	IFT122	GRCh38.p7	3:129446035	GCCATGATGGGAAAT[-/GGG]GGTCAAACATGCCTC	55764
rs750880494	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129460349	GTTATTTCATTTCAC[G/T]TAATGTCCTCAAGGC	55764
rs750896392	snp	C/G	4.94287e-05	0.00497111	intron-variant	IFT122	GRCh38.p7	3:129449980	AAGTGCTTCCCTAAC[C/G]TCCCTCTTGTGAGTA	55764
rs750912015	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129504399	GCTAGCAGAGAACGA[C/T]CGCTTTGAGGAAGCC	55764
rs750993030	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464707	ACGGAACAAAAATGG[C/T]GAGGAGAAAGTAAAG	55764
rs750995900	snp	C/G	1.65217e-05	0.00287412	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507781	AGGTGGCTGGGTCAC[C/G]AGCACCTGAGGGTAC	55764
rs751025977	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454097	CTGATGGGCCTCTTT[A/G]ATAATCAGATGGAAG	55764
rs751039633	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129496402	TGAGGGTCTTCCTTC[C/T]ATCAAGGGGCTTTGT	55764
rs751077606	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441335	TGAACATCCTTCAAG[A/G]CTCACGTTGGAGACG	55764
rs751078896	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129453296	TTCCATTTTTTTTTT[-/C]TTCAGTGAAATAGGA	55764
rs751097764	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129515054	CAGACCTGGGTTCAC[A/G]TCCCGGCTCCACCCT	55764
rs751139167	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475729	TGAGGCAGGAAGATC[A/G]CTTGAGTCCAGGAGT	55764
rs751162653	snp	A/G	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476402	CTGGGGGGTTCAGAC[A/G]AGCAAGTATCTCTTT	55764
rs751165656	snp	C/T	2.31318e-05	0.00340079	intron-variant	IFT122	GRCh38.p7	3:129461012	CTGGCCAAAAGTGAG[C/T]CCCCATCTCTACAAA	55764
rs751207893	snp	G/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440645	TGTCGCTGCCTTGGA[G/T]TCATCTCACACCCAC	55764
rs751216192	snp	G/T	1.72901e-05	0.0029402	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476283	TGGATTCGGAAATGG[G/T]TTTTCCCTTGCTGTG	55764
rs751216208	snp	C/G	0.000156159	0.00883489	missense	IFT122	GRCh38.p7	3:129481609	GCTGCTTGGACATGA[C/G]TGCCTCCCGTAAGAA	55764
rs751262275	snp	C/G	1.83656e-05	0.00303026	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520181	CTTCCCTTAGATGTT[C/G]CATTCTGAGGACTAT	55764
rs751279928	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477010	GATCTCATGAAAGCA[A/G]TAAATCCTCTCTGAA	55764
rs751290587	snp	G/T	5.80939e-05	0.00538921	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439735	AGTAACTTACCGGAG[G/T]TCATTCGGCGGGTCT	55764
rs751297699	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129442352	TGGTTGTTGTTACTA[C/T]GGATAGTAATAAAAT	55764
rs751338226	snp	C/G	1.64841e-05	0.00287085	missense	IFT122	GRCh38.p7	3:129502778	CTGTGCGCTACCTAC[C/G]TCAAGAAGCTGGACA	55764
rs751342507	snp	A/G/T	8.57323e-05	0.00654673	intron-variant	IFT122	GRCh38.p7	3:129488170	GGGTAATCATCCCAC[A/G/T]CATCTGGAGGCAGGC	55764
rs751378587	snp	A/G	1.64827e-05	0.00287073	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461232	TTACTTCCCAGGCAC[A/G]ATGATGCTATACAAT	55764
rs751441796	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129452536	TGTGCCAGTGGGCAT[-/C]GGGGGGAAGAGAGCT	55764
rs751444342	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508330	ATGGGTTGTCAACAG[C/T]CTCTTCATCCACTGT	55764
rs751459079	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129468047	GGCTCACTGGTGGGC[G/T]GGGCTCCTGGATTGT	55764
rs751478041	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129487321	CATACATGTGGCAGG[-/A]AAGGGGCACAGAACC	55764
rs751478153	snp	G/T	2.24565e-05	0.00335078	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439858	TCCGGCTGCAGCAAC[G/T]AGCCCAGCGCCGCAA	55764
rs751483019	snp	G/T	1.64806e-05	0.00287054	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478155	CCGGGTAAAGGAGAA[G/T]ATTATCAAGAAGTTT	55764
rs751483616	snp	C/T	2.20631e-05	0.00332131	missense	IFT122	GRCh38.p7	3:129515516	TGTGCTACCGCTGCT[C/T]CACCAACAACCCGCT	55764
rs751522806	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129466064	CCACCCACCTCAGCC[-/T]TCCCAAAGTGCTGAG	55764
rs751526040	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129483431	CTGAAATGTGTGAGC[A/G]CTGACCAAGCCCAGG	55764
rs751536818	snp	C/T	7.22439e-05	0.00600972	intron-variant	IFT122	GRCh38.p7	3:129515454	AGGACACGTGCCTGC[C/T]CCGGCCCCTCGGGAG	55764
rs751543010	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468997	GTATGTAAGAGAAAA[A/G]CAGTCTCAATATTGC	55764
rs751575983	snp	C/T	1.6476e-05	0.00287014	intron-variant	IFT122	GRCh38.p7	3:129488238	AGTCTTCTTTTTTTC[C/T]CTTGATGAAATCCTG	55764
rs751608029	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129448506	CCCTAATCTTTTATT[-/A]ATGCAGTTGGGTTAT	55764
rs751713457	snp	A/G	1.65023e-05	0.00287244	intron-variant	IFT122	GRCh38.p7	3:129458690	CACGTAAGTAACTTA[A/G]GTGTACAGTATTATG	55764
rs751753419	in-del	-/G	1.64739e-05	0.00286996	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464733	AAAGATCGAGCGGCC[-/G]GGGGGGCTCCCTCTC	55764
rs751755339	snp	A/G	1.64792e-05	0.00287042	intron-variant	IFT122	GRCh38.p7	3:129495625	AACCTACCCTGTCCC[A/G]GGCCCAAGCTCCAGC	55764
rs751764467	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516288	CAGATTGCTCCTGCA[-/CA]CACACACACACACAC	55764
rs751769859	in-del	-/C	0.231589	0.249321	intron-variant	IFT122	GRCh38.p7	3:129478265	AATTCCATTTGTGCT[-/C]CCCCCCCCAGTGATA	55764
rs751777295	snp	C/G	1.64749e-05	0.00287005	missense	IFT122	GRCh38.p7	3:129499918	ATTTCCTTGGATCTG[C/G]AGACCCCAAAGAAAC	55764
rs751795805	snp	A/T	3.29522e-05	0.00405894	missense	IFT122	GRCh38.p7	3:129519140	TAGTGGAGACCAAGG[A/T]CTCCATCGGAGATGA	55764
rs751803328	snp	A/G	1.64871e-05	0.00287111	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458588	ACTTTCCATTTTACA[A/G]ACACTTTTAGGCAAG	55764
rs751861845	in-del	-/CTT			intron-variant	IFT122	GRCh38.p7	3:129505605	AGGCCAGACCTTCTC[-/CTT]CTCTGAAGGCGGAGG	55764
rs751879590	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456847	CTTGAACCCGGGAGT[C/T]GGAGGTTGCGGTGAG	55764
rs751889777	in-del	-/AA			intron-variant	IFT122	GRCh38.p7	3:129498741	CATGGGGAAAGGAGT[-/AA]GCTTTTTTTGTTCTC	55764
rs751910107	snp	A/T	1.66153e-05	0.00288225	missense	IFT122	GRCh38.p7	3:129514400	GCAGGAAAATACTCT[A/T]CACCTTGGCCAAGCA	55764
rs751960290	snp	A/G	3.35312e-05	0.00409444	intron-variant	IFT122	GRCh38.p7	3:129463510	TTCCTTTTTATTGCT[A/G]GGTAGTATTCCAACC	55764
rs751967135	snp	C/T	4.99555e-05	0.00499752	intron-variant	IFT122	GRCh38.p7	3:129519548	GAGGACACTGTGCCT[C/T]CTTCCCGCCCACCCT	55764
rs751973489	snp	C/T			intron-variant, missense	IFT122	GRCh38.p7	3:129506744	GAATGGTATGAGGAC[C/T]GTCCTGGGGTTATGG	55764
rs751979422	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129496940	GTAGAATTTAGGGTT[A/G]GGAACCCCTGAGGCC	55764
rs752012459	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129449417	TTTGTGAAAGTGTCT[C/G]TTTCACACCTTCTCA	55764
rs752059958	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129519240	CTCCATCCCTTCTCC[G/T]GTGCACATGGGGACC	55764
rs752071054	snp	C/G	1.64762e-05	0.00287016	intron-variant	IFT122	GRCh38.p7	3:129519100	ATCCTTGACCAGATC[C/G]CTCCAGGCTCCCAGA	55764
rs752080750	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129468491	CTGGGATTACAGACA[C/T]GCGACACCACGCCGA	55764
rs752149043	snp	C/T	3.29451e-05	0.00405851	intron-variant	IFT122	GRCh38.p7	3:129492138	TTTATTTCTTCGCCA[C/T]AGGCCTTCATCAGAG	55764
rs752162333	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129490736	GCTTTGCAGGGTTGC[C/G]CTCTCAAGGCGCTTT	55764
rs752171223	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129500544	ATGGTAGGAACAAAA[A/C]CAAAACAAGTTCCAA	55764
rs752186033	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443319	GAGGACAATTTGCAG[A/G]ATTCCTCTGTATCTC	55764
rs752204858	snp	C/T	3.54208e-05	0.00420822	intron-variant	IFT122	GRCh38.p7	3:129515637	TGTGGGTGGGACAGC[C/T]TGTGGACAGCCAGGC	55764
rs752213678	snp	C/G	4.94189e-05	0.00497062	intron-variant	IFT122	GRCh38.p7	3:129449854	CTAATTGTCTTTTTC[C/G]CTTGTCTTCTGTTCA	55764
rs752230588	snp	C/T	1.6473e-05	0.00286988	splice-donor-variant	IFT122	GRCh38.p7	3:129449939	GAAGCAGATTACTGG[C/T]AGGATTTTGTCTTAG	55764
rs752254170	in-del	-/GTT			intron-variant	IFT122	GRCh38.p7	3:129463471	TGGAGATCCATCTAA[-/GTT]GTTGTATGTTTCAAT	55764
rs752262810	snp	C/T			intron-variant, missense	IFT122	GRCh38.p7	3:129503579	CCTCCCCCGACTCAC[C/T]CACCCACCCATCATG	55764
rs752268115	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129477170	TTCTGGTCAGAGTCA[A/C]TCTGGGGTGCTTCTC	55764
rs752275533	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505165	CAGCTGTGCAAGGAC[A/G]AAGAGGCTAAATGTG	55764
rs752326839	snp	C/G/T	7.48817e-05	0.0061185	intron-variant	IFT122	GRCh38.p7	3:129481513	GACTGACACTGTTTT[C/G/T]GCTGAAATTTTGCCA	55764
rs752356135	snp	A/C/G/T	7.20911e-05	0.00600346	intron-variant	IFT122	GRCh38.p7	3:129478270	CCATTTGTGCTCCCC[A/C/G/T]CCCAGTGATAGGGTG	55764
rs752368761	snp	A/G	6.58913e-05	0.00573945	missense	IFT122	GRCh38.p7	3:129500053	AGATCTGTGGTGACC[A/G]TGGCTGGGTTGACAT	55764
rs752373667	snp	A/G	4.94189e-05	0.00497062	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469358	GAGGAACGTAATGAC[A/G]TCCTGGCTGTGGCTG	55764
rs752381952	snp	A/G	1.73333e-05	0.00294386	intron-variant	IFT122	GRCh38.p7	3:129495401	TAAAGGCTGCTTCCT[A/G]CCCATGGCTGCAGAG	55764
rs752384839	snp	A/G	1.64996e-05	0.0028722	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507755	ACCATGCCATCCATC[A/G]CCACACGGTAAGGTG	55764
rs752408411	in-del	-/TC			intron-variant	IFT122	GRCh38.p7	3:129508710	TCTTGGAAAGCATTT[-/TC]TGCATCCTGCTGGTT	55764
rs752426586	snp	C/T	0.000527139	0.0162263	intron-variant	IFT122	GRCh38.p7	3:129479943	TGCTCCCTCACGTCT[C/T]CTGTCAGGCTGATAA	55764
rs752437724	snp	C/G	1.64857e-05	0.00287099	synonymous-codon	IFT122	GRCh38.p7	3:129517482	AGACGTGCTACACCT[C/G]GTTGAGTTCTACCTG	55764
rs752442380	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469197	GATGGGTTGGGCCAA[A/G]TTATAACTTTTGGCT	55764
rs752504797	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511742	TGGGTCAGCAGTTGA[A/G]GAACTCCGCATGTGT	55764
rs752578714	snp	C/T	1.64738e-05	0.00286995	missense, intron-variant	IFT122	GRCh38.p7	3:129460885	TCTTCATTGCACCTC[C/T]ATCTTCCATTTCTGG	55764
rs752588840	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129454736	GGTGCCTCTGGTGTT[A/T]ATAAGCATAGCAGGG	55764
rs752602061	snp	C/T	4.18366e-05	0.00457346	synonymous-codon	IFT122	GRCh38.p7	3:129483625	TGTGGTCGGCTACAA[C/T]GGCTCCAAGATCTTC	55764
rs752614515	snp	G/T	1.64879e-05	0.00287118	intron-variant	IFT122	GRCh38.p7	3:129461221	TCTACAGTTGTTTAC[G/T]TCCCAGGCACAATGA	55764
rs752668104	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129442610	AGTAGAACTAAAAAA[A/G]TCCTAGATGTCAAAG	55764
rs752676257	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129455413	CCTGACCTCGTGATC[C/T]GCCCACCTCGGCCTC	55764
rs752677018	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457234	CAAATTACTTGTTAT[A/C]TGTTGCCTCTCTCCA	55764
rs752679437	snp	C/G	0.00017619	0.00938423	intron-variant	IFT122	GRCh38.p7	3:129515445	AGGGGGAGGAGGACA[C/G]GTGCCTGCCCCGGCC	55764
rs752703596	snp	A/G	1.86194e-05	0.00305112	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460980	TGATTGCTTGAGGCC[A/G]AGCGTTCAAAACCAA	55764
rs752704373	snp	C/T	4.97146e-05	0.00498546	intron-variant	IFT122	GRCh38.p7	3:129502689	CAGAGCCCACCCTCC[C/T]ACCTGCCCCTTCCCT	55764
rs752731495	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459642	TCCTTCCTTCCCTCC[C/T]TCCCTCCCTTCTTCC	55764
rs752745361	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129489539	GAGATGGAGGAGGCT[A/G]TAAGAATTCAGAGGA	55764
rs752763145	in-del	-/G	3.33111e-05	0.00408099	intron-variant	IFT122	GRCh38.p7	3:129502886	GCTGGGATGAGGTGA[-/G]GGGGAAAGCAGGCCT	55764
rs752782346	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501524	GATTTTGTTCCCCAC[A/G]TTATTCTTTAAATGA	55764
rs752786740	snp	A/C	3.82665e-05	0.00437399	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520169	TCTTACAGCTGTCTT[A/C]CCTTAGATGTTCCAT	55764
rs752804124	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451997	GGCATATGCGAAGGA[C/T]GGTAAAAGGCTGCTC	55764
rs752823438	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129477714	CAGGCTTCTGATCAC[C/G]GGGGGCCACTAGTGC	55764
rs752826173	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456890	CACTGCACTATAGCC[C/T]GGGCAACAGAGTGAG	55764
rs752834481	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129519246	CCCTTCTCCTGTGCA[C/T]ATGGGGACCCTCAGC	55764
rs752835806	snp	A/G	1.64814e-05	0.00287061	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478132	GAGGACTTATCAGAC[A/G]TGCATTACCGGGTAA	55764
rs752858175	snp	C/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466947	CGAGGATGTCATTGT[C/G]AACAGATATATTCAG	55764
rs752885341	snp	A/G	6.8099e-05	0.0058348	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439723	CCAAAAGGGGACAGT[A/G]ACTTACCGGAGGTCA	55764
rs752905188	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129450662	CTTTTCCAATACTCT[A/T]ACCATTTCAGAAAGT	55764
rs752911061	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457991	GATCCACCCGCCTCA[C/G]CCCTCCAAAGTGCTG	55764
rs752937638	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493164	CAGTGCTGTCTGGCT[A/G]TCTGTTAAAAGGCAT	55764
rs752946165	snp	A/G	1.64879e-05	0.00287118	intron-variant	IFT122	GRCh38.p7	3:129464822	AGAACAAACACCATC[A/G]TGAAGAAGGGCTTTT	55764
rs752961918	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506494	GGAGAGCAGGTTTAA[C/T]GATGCTGCCTATTAT	55764
rs752975420	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129515005	CTTCTTTCACACATC[C/T]TCCCTCAAGCTCAGA	55764
rs752995189	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452157	TGGTCATTCAATCTA[A/G]CAAGTATTTATTGAG	55764
rs753023444	in-del	-/TCTACTTCCTCTTC			intron-variant	IFT122	GRCh38.p7	3:129450489	CTCTTTCTGTCTAAG[-/TCTACTTCCTCTTC]TCTGTTGTCTCTAGA	55764
rs753028853	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509104	GGAGCTGGTCATCAC[A/G]GTTGTCATGTAAAGT	55764
rs753033587	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129512661	GGTCTCTGGCCAACA[C/T]ACTGTCCCAATCCCT	55764
rs753054926	snp	C/T	1.64789e-05	0.0028704	intron-variant	IFT122	GRCh38.p7	3:129495614	TATGCCAAGGTAACC[C/T]ACCCTGTCCCAGGCC	55764
rs753055277	snp	C/T	1.66214e-05	0.00288278	synonymous-codon	IFT122	GRCh38.p7	3:129481649	GGTAGATGAAAATGA[C/T]ACTTGCCTGGTGTAT	55764
rs753066226	snp	A/G	0.000148754	0.00862293	missense	IFT122	GRCh38.p7	3:129519127	CAGATTCTGCGGCTA[A/G]TGGAGACCAAGGACT	55764
rs753081097	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129500645	GGGACCTTAAAGAAT[C/T]CCAAGAGGTAAATAG	55764
rs753082442	in-del	-/GGACGACAGTCCCAG	1.65089e-05	0.00287301	intron-variant, cds-indel	IFT122	GRCh38.p7	3:129467040	AGAACCAGAGGAAGA[-/GGACGACAGTCCCAG]GGACGACAACTTGTG	55764
rs753092247	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451719	GGTCACATAGTACAT[A/G]GACCTGGGTCCTCTA	55764
rs753097027	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129450851	TCAGCCTCCTGAGTA[C/G]CTGGGACTACAGGCG	55764
rs753112858	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129485349	TCTTCTAAGTTGATG[A/T]TACCCTCGAAACTCA	55764
rs753125279	snp	A/G	1.64749e-05	0.00287005	intron-variant	IFT122	GRCh38.p7	3:129476618	AATGGGGGAATGCAG[A/G]CTTTCTCCAGAGAGC	55764
rs753153417	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490400	GAGCTGCTGAGCTCC[C/T]GCCAGACCCTGAGCA	55764
rs753153479	snp	G/T			downstream-variant-500B	IFT122	GRCh38.p7	3:129520920	CCAGGCTCTGGAGCC[G/T]CCCTCTTCCATCCAC	55764
rs753172135	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439629	CTTCGAGGTTTCTGC[C/T]GACCCTCTGTCAAAG	55764
rs753193342	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438176	GGAAATCTCTGCACA[A/G]CAAAAAAGTCAAGCT	55764
rs753194674	snp	A/G/T	3.33301e-05	0.00408218	intron-variant	IFT122	GRCh38.p7	3:129519543	TGAGTGAGGACACTG[A/G/T]GCCTCCTTCCCGCCC	55764
rs753198521	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472654	TTTTGGCCATGATTT[C/T]TTGAAATATTTCTTC	55764
rs753208637	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129515066	CACATCCCGGCTCCA[-/C]CCTCTCCTAGCTCTG	55764
rs753219859	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129508251	AAGTAGTTCTTTTTA[A/G]TCACTCCCTGATTCC	55764
rs753232109	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129466606	TCCCAGGTTCAAGCA[A/T]TCCTCTCACCTCAGC	55764
rs753243209	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129492736	TTGTCATCCAAACCC[A/C]ATAGGCCTGCAGTGT	55764
rs753272793	in-del	-/ATCTTCGTGGACA	3.75192e-05	0.00433107	frameshift-variant	IFT122	GRCh38.p7	3:129481539	TGCCAGATCCTGAAG[-/ATCTTCGTGGACA]ATCTCTTTGCTATCG	55764
rs753285748	snp	A/G	1.66023e-05	0.00288113	synonymous-codon	IFT122	GRCh38.p7	3:129502882	CCAGCGCTGGGATGA[A/G]GTGAGGGGAAAGCAG	55764
rs753292236	snp	G/T	1.6596e-05	0.00288058	intron-variant	IFT122	GRCh38.p7	3:129481729	CCAGGGACATCATCC[G/T]TTGATTAGAGACTCT	55764
rs753297718	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509320	TTGAGTTCTTCGGCA[A/G]CTTCTCCTGTAGTTG	55764
rs753325449	snp	A/T	3.36022e-05	0.00409877	intron-variant	IFT122	GRCh38.p7	3:129463504	TATTTGTTCCTTTTT[A/T]TTGCTGGGTAGTATT	55764
rs753329365	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484007	TGGAGTGAGCAGCAA[A/G]GCCGGGAGTCCGGCA	55764
rs753332539	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445295	CCTGCTACTGCACTC[C/T]AGCCTGGGTGACAGA	55764
rs753366243	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129454396	TAGACTCTGTCTCTT[-/A]AAAAAAAAAAAAAAA	55764
rs753409384	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129500709	CAGCAGAAACACAGC[A/G]AGTTGGCTCTGGTTG	55764
rs753496135	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129464940	TTTTTTAATAGTCCC[A/G]CTACCTGAGAATGTA	55764
rs753501616	snp	A/G	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129479855	TGGAGTCTCTCATTC[A/G]TTACATCAAGGTGAT	55764
rs753522721	in-del	-/TC			intron-variant	IFT122	GRCh38.p7	3:129505733	GGTACTCAGAAAATA[-/TC]TGTTAAACAGTATAG	55764
rs753530616	snp	A/T	1.80641e-05	0.00300528	intron-variant	IFT122	GRCh38.p7	3:129515621	CCCTGCATCCTGAGC[A/T]TGTGGGTGGGACAGC	55764
rs753542568	in-del	-/CT			intron-variant	IFT122	GRCh38.p7	3:129485700	AAATGCAGTTTGCTG[-/CT]CTCTGACTGTGGCCG	55764
rs753548791	snp	C/T	1.66768e-05	0.00288758	intron-variant	IFT122	GRCh38.p7	3:129463651	GCTCTGACGATAAGA[C/T]TTATGTTCCTTCATC	55764
rs753552899	snp	A/G	4.94197e-05	0.00497066	synonymous-codon	IFT122	GRCh38.p7	3:129488364	ACTGGCCATGGAAGC[A/G]CTAGAAGGTTTAGAT	55764
rs753553299	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129519005	TGGAAAACTCTTCCA[C/T]TGGTCTGGCTGCCCT	55764
rs753553484	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485581	CCATTACAAACCCAC[A/G]CACCACATCCACCAG	55764
rs753571457	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129455531	TAAGACATAGTTTTT[G/T]TGTTCAAGAAAAACA	55764
rs753594527	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129501728	AGGTGTCTTTCCTCC[A/C]GGGACGTTGGGTGTG	55764
rs753620781	snp	A/T	1.64966e-05	0.00287194	missense	IFT122	GRCh38.p7	3:129517469	CTCTATGCCCTCCAG[A/T]CGTGCTACACCTGGT	55764
rs753626217	snp	A/C/T	8.24061e-05	0.0064185	intron-variant	IFT122	GRCh38.p7	3:129461308	CCAGTGACTTTGGTA[A/C/T]GTTCTGATTCCTGAT	55764
rs753663017	in-del	-/ATG			intron-variant	IFT122	GRCh38.p7	3:129464117	AATGCACACAAACTC[-/ATG]AGTGTAAAGCGTGCA	55764
rs753688569	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512789	TGTTTGTTCAGCCCA[A/G]GTATACATAGCACCT	55764
rs753716636	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129443412	GAGAGAGAACCATCC[C/T]ACAGTAGAATAGACT	55764
rs753730397	snp	A/T	3.40611e-05	0.00412667	intron-variant	IFT122	GRCh38.p7	3:129467072	ACGACAACTTGTGAG[A/T]GTGTCCCAGTGAGTG	55764
rs753751181	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456740	CCCAACATGGAGAAA[C/T]CCCATCTCTACTAAA	55764
rs753777774	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129490936	GCCTCCCACCCCTGC[A/T]CATGCTCAGACCATT	55764
rs753778793	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129492374	GGGGAGACAACAGCA[C/G]GTAGTGTGAGCTGTT	55764
rs753822017	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129450873	CTACAGGCGCCTGCC[A/G]CTACGCTCAGCTAAT	55764
rs753825998	snp	A/G	1.65364e-05	0.0028754	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129519735	CTCCTGCTTCCAGGT[A/G]GGTGGCCACCCTGGT	55764
rs753835808	snp	C/T	3.29843e-05	0.00406092	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507742	CTGTACCATGGTTAC[C/T]ATGCCATCCATCGCC	55764
rs753917533	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481088	TTTTTTTTAAACCAG[A/G]GATATCAGTAAATGA	55764
rs753932809	snp	A/G	8.26344e-05	0.00642731	missense	IFT122	GRCh38.p7	3:129514469	CCTATGACAAGCTGC[A/G]TGGCCTGTACATCCC	55764
rs753952779	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129459927	CCAGGCCAATTTTTA[A/C]ATTTTTTTTTTTCTT	55764
rs753953371	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464721	GCGAGGAGAAAGTAA[A/G]GATCGAGCGGCCGGG	55764
rs753993269	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129494335	ACAGGTGTAAGCCAC[C/T]ATGTCCAGCCAAAAT	55764
rs754006580	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520051	AAACAAAGGTGCTGC[A/G]GGTCTGTGTCCAGCC	55764
rs754034427	snp	A/G	0.000355261	0.0133231	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460962	AGGCCAAGGTGGGAG[A/G]ATTGATTGCTTGAGG	55764
rs754037158	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129447940	TAAAAGAGCCCTGGT[C/T]GAGGAGGAAGTCCAT	55764
rs754061139	snp	A/C	1.67128e-05	0.00289069	intron-variant	IFT122	GRCh38.p7	3:129478007	ACTAGATATTTTTTT[A/C]TTTGACAGTTCGGAT	55764
rs754081292	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129496025	CGACATGGTGCCTGC[C/T]AGCCAAGTTTCCCAT	55764
rs754093796	snp	C/G	3.56056e-05	0.00421918	intron-variant	IFT122	GRCh38.p7	3:129483731	GCAAGGCTGACAAGA[C/G]CAGGGAAGCTGGGCC	55764
rs754107579	snp	C/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504403	GCAGAGAACGATCGC[C/T]TTGAGGAAGCCCAGA	55764
rs754172386	snp	G/T	3.33306e-05	0.00408218	missense	IFT122	GRCh38.p7	3:129495448	CTAATTTTTCCAGGA[G/T]AGGAAGAAGCGGGGA	55764
rs754215295	snp	C/G/T	6.7368e-05	0.0058034	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439857	GTCCGGCTGCAGCAA[C/G/T]GAGCCCAGCGCCGCA	55764
rs754216600	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486477	CACAACTAAATTGCA[A/G]CAGGCTGTACTTACT	55764
rs754223819	in-del	-/GT	1.89586e-05	0.00307879	frameshift-variant	IFT122	GRCh38.p7	3:129483614	CTGCAGGGCTTTGTG[-/GT]CGGCTACAATGGCTC	55764
rs754227793	snp	G/T	0.000185787	0.00963634	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129456114	CATTTTTCAAATAAG[G/T]AAATGAAAGCTCTTC	55764
rs754242854	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129452771	TTTAAAAGGATCCCT[C/G]TAGTTGCTGAGTTGG	55764
rs754266082	snp	G/T	1.6483e-05	0.00287076	intron-variant	IFT122	GRCh38.p7	3:129464800	CTCTTAAAGTTGTCC[G/T]CCTTCTAGAACAAAC	55764
rs754275024	snp	A/G	3.44021e-05	0.00414727	missense	IFT122	GRCh38.p7	3:129481618	ACATGAGTGCCTCCC[A/G]TAAGAAGCTGGCCGT	55764
rs754283229	snp	C/G	0.000115305	0.00759205	missense	IFT122	GRCh38.p7	3:129512356	AACTCTTTTCAACAT[C/G]TCCAGGTTCCTGCTG	55764
rs754297631	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469061	GCTCTGAAATGAGAG[A/G]TTTATCTTCTTCAGC	55764
rs754306467	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473744	TGCTGTGGTCCTCCC[A/G]AATTCTATACTCACC	55764
rs754315013	in-del	-/C	3.29669e-05	0.00405984	intron-variant	IFT122	GRCh38.p7	3:129506365	CCTCCTGTGTGACTT[-/C]CTAAATAGCATGTGC	55764
rs754333037	snp	A/G	1.64762e-05	0.00287016	missense	IFT122	GRCh38.p7	3:129519115	CCTCCAGGCTCCCAG[A/G]TTCTGCGGCTAGTGG	55764
rs754356431	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458408	ACATCTTTGTTTACT[C/T]AGTGTCAGACAAAGC	55764
rs754375621	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510083	ATTTCTCTTTTTTCA[A/G]AGATGAGGTCTCTGT	55764
rs754388967	snp	C/T	4.94238e-05	0.00497086	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451990	ACTGTGTGGCATATG[C/T]GAAGGATGGTAAAAG	55764
rs754396913	snp	C/G	5.58998e-05	0.00528647	synonymous-codon	IFT122	GRCh38.p7	3:129481547	CCTGAAGATCTTCGT[C/G]GACAATCTCTTTGCT	55764
rs754414788	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454172	CAGAATTTCATGCAT[A/G]TAATTTTAGTCTGAT	55764
rs754419382	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517219	CACAGACTGCCCCTG[-/CA]CACACACACACACAG	55764
rs754443733	snp	G/T	4.801e-05	0.00489925	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439882	GCCGCAACGCCCAGG[G/T]TGTGGGGCGGAGTAA	55764
rs754449933	in-del	-/A	6.63097e-05	0.00575764	intron-variant	IFT122	GRCh38.p7	3:129507810	ACCATCTCCTGAGCT[-/A]GGGGTCCCGGGCATA	55764
rs754451883	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438795	AACAAGCAACCGGGC[A/G]TGGTGGAGCATACCT	55764
rs754465256	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129509192	ATAAGAAAAGACAAC[A/C]CTTCAAAACGACTAT	55764
rs754476745	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129466296	AATTTTTTTTGGCCC[A/G]TGCTGTACCATGCAT	55764
rs754494004	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487718	CAAACGTAGACTGGG[A/G]TTCTGCTGAGGGAGG	55764
rs754526534	snp	C/G	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129506544	AGTGCCTCGATATAG[C/G]TCAAGGTGTGTAAAC	55764
rs754532829	snp	C/T	5.87941e-05	0.00542159	synonymous-codon	IFT122	GRCh38.p7	3:129515541	CCCGCTGCTCAACAA[C/T]CTGGGCAACGTCTGC	55764
rs754541880	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129442208	TTCATTTCTCTCTTG[C/T]GGTACTTCCAGAGTC	55764
rs754599835	snp	C/T	1.64738e-05	0.00286995	intron-variant	IFT122	GRCh38.p7	3:129449847	TTGGTTCCTAATTGT[C/T]TTTTTCCCTTGTCTT	55764
rs754620710	snp	G/T	1.79515e-05	0.00299591	intron-variant	IFT122	GRCh38.p7	3:129515627	ATCCTGAGCATGTGG[G/T]TGGGACAGCCTGTGG	55764
rs754652142	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129460453	TTCTTTATTATTATT[A/T]TTTTTTATGAAGACG	55764
rs754719725	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466729	GCTGGTCTTGAACTC[C/T]TGATCTCGAGCGATT	55764
rs754782458	snp	A/G	1.64732e-05	0.0028699	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469353	TTAGAGAGGAACGTA[A/G]TGACATCCTGGCTGT	55764
rs754808589	snp	A/G	1.65007e-05	0.00287229	missense	IFT122	GRCh38.p7	3:129519650	ATGTCCTCATCAAGC[A/G]ATGGCCCCCACCCCT	55764
rs754839364	snp	A/G	5.13694e-05	0.00506775	intron-variant	IFT122	GRCh38.p7	3:129467075	ACAACTTGTGAGTGT[A/G]TCCCAGTGAGTGGGA	55764
rs755005244	snp	C/G	3.32685e-05	0.00407837	splice-acceptor-variant	IFT122	GRCh38.p7	3:129478015	TTTTTTTCTTTGACA[C/G]TTCGGATTAAATGCA	55764
rs755020519	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	IFT122	GRCh38.p7	3:129460879	GTGATGTCTTCATTG[C/T]ACCTCCATCTTCCAT	55764
rs755043939	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129472492	TAAGTGGAAAGATAA[G/T]AATTATATTTAAAGT	55764
rs755057372	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471221	TTAGATGTGTGTAGC[C/T]CAGCTTTTGGGCCAT	55764
rs755058078	snp	A/G	2.02231e-05	0.0031798	missense	IFT122	GRCh38.p7	3:129483621	GCTTTGTGGTCGGCT[A/G]CAATGGCTCCAAGAT	55764
rs755060067	snp	A/G	0.000329832	0.0128377	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476793	AGCACCTGATCACTG[A/G]GCAGAAAGGTAAGAG	55764
rs755075432	snp	A/G	1.64732e-05	0.0028699	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504353	AGCATCCTGAGTTTA[A/G]GGATGACATCTACAT	55764
rs755091938	in-del	-/G	1.64739e-05	0.00286996	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464734	AAAGATCGAGCGGCC[-/G]GGGGGCTCCCTCTCG	55764
rs755130310	snp	A/G	3.29685e-05	0.00405995	intron-variant	IFT122	GRCh38.p7	3:129464810	TGTCCTCCTTCTAGA[A/G]CAAACACCATCATGA	55764
rs755142655	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443639	AATATGTAGAACATG[A/G]CCATTGCTTTCAAAT	55764
rs755199514	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129491612	TCTTCCAGAATCTGT[C/G]TTTATACCCTCTCAG	55764
rs755244741	snp	A/G	1.84855e-05	0.00304013	missense	IFT122	GRCh38.p7	3:129481552	AGATCTTCGTGGACA[A/G]TCTCTTTGCTATCGT	55764
rs755254772	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451991	CTGTGTGGCATATGC[A/G]AAGGATGGTAAAAGG	55764
rs755261269	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129497084	TCAGGAGGTCGAGAC[C/T]AGCCTGGGCAATATG	55764
rs755271129	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129514714	CCAGCTCCCCTGTGC[-/T]TCCCTGTCCACCTCC	55764
rs755288076	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129513392	AGAGCTCCTTGTTGT[A/T]AGAATTGGCCTCGCT	55764
rs755291768	in-del	-/TTCC			intron-variant	IFT122	GRCh38.p7	3:129459613	TCCTTCCTTCTTTCC[-/TTCC]TTCCTTCCTTCCTTC	55764
rs755306761	snp	A/G	3.29495e-05	0.00405877	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504409	AACGATCGCTTTGAG[A/G]AAGCCCAGAAAGGTA	55764
rs755343458	snp	A/G	3.29478e-05	0.00405867	missense	IFT122	GRCh38.p7	3:129495554	AAGAGGAGTGGGCAC[A/G]AGAACCTCGCGCTTG	55764
rs755362111	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129507995	AGCTGGAATGGGCCT[C/T]GCTAGTTCCTCAGTG	55764
rs755379713	snp	A/G			intron-variant, missense	IFT122	GRCh38.p7	3:129506745	AATGGTATGAGGACC[A/G]TCCTGGGGTTATGGT	55764
rs755389166	snp	A/G/T	3.29491e-05	0.00405877	missense, stop-gained	IFT122	GRCh38.p7	3:129517519	GGGATCACTGATGAA[A/G/T]AAGCCATCTCCCTCA	55764
rs755417739	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	IFT122	GRCh38.p7	3:129512359	TCTTTTCAACATCTC[C/T]AGGTTCCTGCTGCAC	55764
rs755423766	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129497982	TGCTCTTAACTCTTA[C/T]GTAGTATGTTCTTAT	55764
rs755493101	snp	C/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476435	ACCAAGGATGGAGTG[C/T]GGCTTGGGACTGTTG	55764
rs755510563	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484011	GTGAGCAGCAAAGCC[A/G]GGAGTCCGGCAGGGT	55764
rs755545448	snp	C/T	5.07997e-05	0.00503957	synonymous-codon	IFT122	GRCh38.p7	3:129481631	CCGTAAGAAGCTGGC[C/T]GTGGTAGATGAAAAT	55764
rs755556032	snp	A/G	6.59294e-05	0.00574111	missense	IFT122	GRCh38.p7	3:129502793	CTCAAGAAGCTGGAC[A/G]GCCCTGGCTATGCTG	55764
rs755562343	snp	G/T	3.5766e-05	0.00422868	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520218	CTGGTGCTTCAGCAT[G/T]GCTGCTGCCCCTACT	55764
rs755579475	in-del	-/GCGAGTGA	9.88973e-05	0.00703128	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440418	GGTCGAGTCCTCGCG[-/GCGAGTGA]GGGAGTGCGCGAGCC	55764
rs755585099	snp	A/G	1.64779e-05	0.00287031	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461265	GTCTCCTACAATCCT[A/G]TTACTCATCAACTGG	55764
rs755626715	snp	C/T	1.70017e-05	0.00291558	intron-variant	IFT122	GRCh38.p7	3:129488181	CCACGCATCTGGAGG[C/T]AGGCTCTGTATGCAT	55764
rs755650510	snp	G/T	3.2969e-05	0.00405998	intron-variant	IFT122	GRCh38.p7	3:129512451	CCGTCCCACCACCGT[G/T]CTTGTCTAATGGCCC	55764
rs755677495	snp	A/G	3.30229e-05	0.0040633	missense	IFT122	GRCh38.p7	3:129502728	TGATCGACATCGCCC[A/G]CAAACTGGACAAGGC	55764
rs755723373	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129462198	TATAGCATTTTCTTC[A/C]TGTGAAGCACTGGTC	55764
rs755729983	snp	C/T	9.25883e-05	0.00680335	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439874	AGCCCAGCGCCGCAA[C/T]GCCCAGGGTGTGGGG	55764
rs755773879	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129449596	TAGAAGAGTTAATAC[C/G]CTCAACAGTTGACCC	55764
rs755779356	snp	C/G	0.000112034	0.00748362	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439758	GCGGGTCTGGGACTA[C/G]GCGCTCACTAGAGGT	55764
rs755784546	snp	A/C/G	3.29469e-05	0.00405864	intron-variant	IFT122	GRCh38.p7	3:129488251	TCCCTTGATGAAATC[A/C/G]TGCAGTCCGCTCCCA	55764
rs755817744	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129463746	GGTTTAGGCCCCTGT[A/G]TTTCCTTTTTTCTTC	55764
rs755817998	snp	G/T	1.65375e-05	0.0028755	intron-variant	IFT122	GRCh38.p7	3:129461353	TAACTGAAAATCTGG[G/T]CTAAAAATGCTAAAA	55764
rs755824660	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503613	CATTTTAGAGTGAAA[A/G]CAAAGCCTTCACTGA	55764
rs755849779	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512671	CAACACACTGTCCCA[A/G]TCCCTCCTAGAACCC	55764
rs755903501	snp	C/T	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129506535	TGTCCATGCAGTGCC[C/T]CGATATAGCTCAAGG	55764
rs755928571	snp	G/T	0.000131785	0.00811635	missense	IFT122	GRCh38.p7	3:129479840	AGCGGGAGTGGCAGA[G/T]GGAGTCTCTCATTCG	55764
rs755976988	snp	G/T	3.31219e-05	0.00406938	intron-variant	IFT122	GRCh38.p7	3:129458719	TGAGTTTGATGCTTA[G/T]TGAATAATTGCAGCA	55764
rs755983613	snp	C/G	1.64779e-05	0.00287031	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479776	TGCAGAGCTGGGTTT[C/G]CTTCCTAGGAGAAAC	55764
rs756028799	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457435	TTCCATGATGACTCC[A/G]CTCATTCCCTCAGAC	55764
rs756062644	snp	C/T	1.64768e-05	0.00287021	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507649	ACACGTTTCCCCTCC[C/T]ACCCGCTGCACACAG	55764
rs756098804	snp	A/G	1.64808e-05	0.00287057	intron-variant	IFT122	GRCh38.p7	3:129495638	CCAGGCCCAAGCTCC[A/G]GCTTGGAGCCCACTG	55764
rs756108609	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443366	AGTGTGTCTTCTGAC[A/G]GTGTATCTCTTTTAT	55764
rs756137575	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	IFT122	GRCh38.p7	3:129483529	CACCCAGTGTGAGGA[C/T]ATGCTCTGCTTCTCG	55764
rs756151510	snp	C/G	1.64898e-05	0.00287135	intron-variant	IFT122	GRCh38.p7	3:129483449	GACCAAGCCCAGGGT[C/G]GTTCTCACAGGATCC	55764
rs756158894	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456896	ACTATAGCCTGGGCA[A/G]CAGAGTGAGACTTAG	55764
rs756175324	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	IFT122	GRCh38.p7	3:129460862	TTTCCAGATCTTGGT[C/T]TGTGATGTCTTCATT	55764
rs756175676	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458115	ATTAGCTTAATCATT[C/T]TTCAATGTGTATGTA	55764
rs756186737	snp	C/G	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129499955	GCTAATCACCAAACA[C/G]GCTGACTGGGCCAGA	55764
rs756189796	in-del	-/CA			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475520	AGCCAGGCGTGTTCT[-/CA]CACATCTGTAGTCCC	55764
rs756204222	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129493348	CCGAGCTCAGTGGGC[A/C]CAGAGCTGAGGAGGA	55764
rs756254550	snp	A/C	1.65414e-05	0.00287583	missense	IFT122	GRCh38.p7	3:129514415	TCACCTTGGCCAAGC[A/C]GAGCAAGGCCCTCGG	55764
rs756292063	snp	C/T	0.000131811	0.00811715	intron-variant	IFT122	GRCh38.p7	3:129479947	CCCTCACGTCTCCTG[C/T]CAGGCTGATAATCTG	55764
rs756306025	snp	C/T	1.68786e-05	0.002905	intron-variant	IFT122	GRCh38.p7	3:129502909	GCAGGCCTCATGGGC[C/T]GGGGCCCCACCTGAG	55764
rs756309435	snp	A/G	1.65586e-05	0.00287733	missense	IFT122	GRCh38.p7	3:129519571	CCCACCCTGCAGCAA[A/G]GTGGCTCAGAGTTCG	55764
rs756338919	snp	A/G	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129464591	TTTTACCTTCTGTGG[A/G]GTGCTTCCCCTATCC	55764
rs756361469	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129494317	TCCCAAAGTGTAGGG[A/G]TCACAGGTGTAAGCC	55764
rs756366747	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129515072	CCGGCTCCACCCTCT[C/T]CTAGCTCTGTCTCCA	55764
rs756397972	snp	A/G	1.64808e-05	0.00287057	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476768	GATAGCATGACTGAC[A/G]TCATTGTGCAGCACC	55764
rs756427556	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129484023	GCCGGGAGTCCGGCA[C/G]GGTGTGTGTGTGAGT	55764
rs756462117	snp	A/G	1.64732e-05	0.0028699	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504331	CAGGCCTTTGCTTTG[A/G]GTGAGAAGCATCCTG	55764
rs756511809	snp	A/G	6.58892e-05	0.00573936	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449881	TTCAGTATAAATGAC[A/G]TCGCATTTAAGCCTG	55764
rs756533568	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129517041	CAGATTGCTCCTGCA[-/CA]CACACACACACACAC	55764
rs756536945	in-del	-/GAC	3.32928e-05	0.00407987	intron-variant, cds-indel	IFT122	GRCh38.p7	3:129467056	GACGACAGTCCCAGG[-/GAC]GACAACTTGTGAGTG	55764
rs756609110	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440976	TTCTCTAAAACTGGA[A/G]ATGGGCAGGTATGAT	55764
rs756614204	in-del	-/AT			intron-variant	IFT122	GRCh38.p7	3:129517134	CTCCTGCACACACAC[-/AT]GGAGACTGCCCCTGC	55764
rs756631438	in-del	-/TT	1.8431e-05	0.00303565	frameshift-variant	IFT122	GRCh38.p7	3:129481557	TTCGTGGACAATCTC[-/TT]TGCTATCGTCCTGCT	55764
rs756635389	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472679	TTCTTCTTCTCCATT[C/T]TTTCCTTTCCTCTGG	55764
rs756665506	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129492834	TTTTTTTTTTTTTTT[-/C]CTGAAACAAGGTCTC	55764
rs756667874	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129464051	CTGGAGCTTTACGTT[C/T]CTCATCTGACAGATA	55764
rs756679136	snp	C/T	8.2392e-05	0.00641788	intron-variant	IFT122	GRCh38.p7	3:129479960	TGTCAGGCTGATAAT[C/T]TGCATGCACACGTGG	55764
rs756694669	snp	A/G	1.6473e-05	0.00286988	missense	IFT122	GRCh38.p7	3:129512352	CTGAAACTCTTTTCA[A/G]CATCTCCAGGTTCCT	55764
rs756706273	snp	A/C/G	3.29741e-05	0.00406031	intron-variant	IFT122	GRCh38.p7	3:129449989	CCTAACCTCCCTCTT[A/C/G]TGAGTACTCTGAAAT	55764
rs756707339	snp	A/G	1.71879e-05	0.00293149	intron-variant	IFT122	GRCh38.p7	3:129495416	GCCCATGGCTGCAGA[A/G]GCCATTTCCTTTGCT	55764
rs756714116	snp	C/T	1.71528e-05	0.0029285	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476287	TTCGGAAATGGTTTT[C/T]CCCTTGCTGTGTGTT	55764
rs756718708	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468644	CCATCACGGGCTGCC[A/G]CTTTTCTCTTGAACT	55764
rs756735598	snp	A/C/G	3.29464e-05	0.00405861	intron-variant	IFT122	GRCh38.p7	3:129517632	CCTGTGTGTGCGGCT[A/C/G]TGTGAGGGGTCTGGG	55764
rs756738317	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129479478	AGTTAGAACTCCAAG[C/T]GGTTTAGGGTTGCTA	55764
rs756768924	in-del	-/CACACACACACAGACTGCCCCTG			intron-variant	IFT122	GRCh38.p7	3:129517050	TCCTGCACACACACA[-/CACACACACACAGACTGCCCCTG]CACACACACACAGAG	55764
rs756772676	snp	A/G/T	7.46344e-05	0.00610839	missense	IFT122	GRCh38.p7	3:129481545	ATCCTGAAGATCTTC[A/G/T]TGGACAATCTCTTTG	55764
rs756798452	snp	A/G	3.29478e-05	0.00405867	intron-variant	IFT122	GRCh38.p7	3:129500071	GCTGGGTTGACATGT[A/G]GGTTTTGGTCCCTGC	55764
rs756817910	snp	A/G	0.000132223	0.00812981	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507785	GGCTGGGTCACCAGC[A/G]CCTGAGGGTACCATC	55764
rs756819112	snp	C/T	0.000281641	0.0118634	intron-variant, missense	IFT122	GRCh38.p7	3:129519776	TGCTTCTCTTGGCCA[C/T]TTTTCCCTTGCCCAA	55764
rs756824204	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129465005	TTAGGAATGAATCCT[A/G]GACATTTTAGCAAAG	55764
rs756837907	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129486095	AAGATAAAGTATAGC[C/T]CAGAGAGTATTTGTT	55764
rs756861465	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129451214	AGGGATCTTCCCACC[C/T]CAGCCTCCCGAGTAG	55764
rs756909453	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129485593	CACGCACCACATCCA[C/G]CAGGAACTCATCTCC	55764
rs756919471	snp	C/T	2.3738e-05	0.00344506	intron-variant	IFT122	GRCh38.p7	3:129461016	CCAAAAGTGAGTCCC[C/T]ATCTCTACAAATAAG	55764
rs757012267	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129455546	TTGTTCAAGAAAAAC[A/T]ATATAATATGAAGAA	55764
rs757032687	snp	C/G	5.31759e-05	0.00515608	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439742	TACCGGAGGTCATTC[C/G]GCGGGTCTGGGACTA	55764
rs757035295	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439916	GTGAAACCTCTTCAG[C/T]TCACGGCACCGGGCT	55764
rs757095438	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129491096	CCGAGACATGTTTCT[C/T]CCTGGGTCCTCAGTC	55764
rs757096743	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129443414	GAGAGAACCATCCTA[C/T]AGTAGAATAGACTGC	55764
rs757111399	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129444426	ACAACTTGCCTCTCT[C/G]TACTTTAGTTTCCTC	55764
rs757121153	snp	G/T	1.7903e-05	0.00299185	stop-gained, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520197	CATTCTGAGGACTAT[G/T]AGTTGCTGGTGCTTC	55764
rs757121422	snp	A/T	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466957	ATTGTCAACAGATAT[A/T]TTCAGGAAATCCCTT	55764
rs757124316	snp	C/G	4.27487e-05	0.00462304	synonymous-codon	IFT122	GRCh38.p7	3:129515520	CTACCGCTGCTCCAC[C/G]AACAACCCGCTGCTC	55764
rs757125452	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129477445	TTTGCAAGGGATCCA[C/G]GTTGGGGGTTGTCTT	55764
rs757181186	snp	C/T	1.64825e-05	0.00287071	intron-variant	IFT122	GRCh38.p7	3:129479763	TGTTGAATTTCCATG[C/T]AGAGCTGGGTTTGCT	55764
rs757191048	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129501580	GCAGATTTAGGGTGC[C/T]CTGTTCTCTCTTCTG	55764
rs757251769	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129512817	CCTTCTGTGCCCCAA[G/T]CCCTGGGCCAGGCAC	55764
rs757286584	snp	A/T	1.64743e-05	0.00287	intron-variant	IFT122	GRCh38.p7	3:129466883	AACAACTACTTACTG[A/T]CTACAGCCGATGGGA	55764
rs757291049	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129446546	ATAAGCTCAACCAAT[A/T]GTCAGAAAAATTTTA	55764
rs757308965	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129447970	TTCAGACGGTTGGGG[A/G]GGCTTACAATTTTAT	55764
rs757315066	snp	A/C	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129495566	CACGAGAACCTCGCG[A/C]TTGAAATGTACACCG	55764
rs757341742	snp	C/T	4.94376e-05	0.00497156	intron-variant	IFT122	GRCh38.p7	3:129495630	ACCCTGTCCCAGGCC[C/T]AAGCTCCAGCTTGGA	55764
rs757362896	snp	A/C	1.64727e-05	0.00286986	stop-gained	IFT122	GRCh38.p7	3:129506512	TGCTGCCTATTATTA[A/C]TGGATGCTGTCCATG	55764
rs757371697	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129494366	CAATCTTTTATCTCA[C/T]GGCAAGATTTCAATT	55764
rs757380365	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129491090	CAGGGGCCGAGACAT[C/G]TTTCTCCCTGGGTCC	55764
rs757396319	snp	A/G	1.64762e-05	0.00287016	missense	IFT122	GRCh38.p7	3:129519145	GAGACCAAGGACTCC[A/G]TCGGAGATGAGGACC	55764
rs757399965	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509241	CTCATGAGGCACCCA[C/T]TTATCAAGCTTTTTC	55764
rs757443479	snp	A/G			downstream-variant-500B	IFT122	GRCh38.p7	3:129520563	CCGATCTGTCAGACC[A/G]TTAGCATGTACATTT	55764
rs757485649	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129477648	CATGTCTTCCCCGTT[-/TG]TGTCAAGGAGGTGGG	55764
rs757487801	snp	C/T	3.32651e-05	0.00407817	intron-variant	IFT122	GRCh38.p7	3:129519554	ACTGTGCCTCCTTCC[C/T]GCCCACCCTGCAGCA	55764
rs757499045	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129482700	AGCTGACCTGGGCTT[G/T]GGTCCTGCCTGCATC	55764
rs757534122	snp	C/T	3.35835e-05	0.00409764	intron-variant	IFT122	GRCh38.p7	3:129502900	GAGGGGAAAGCAGGC[C/T]TCATGGGCTGGGGCC	55764
rs757569111	snp	C/T	1.64901e-05	0.00287137	intron-variant	IFT122	GRCh38.p7	3:129483443	AGCGCTGACCAAGCC[C/T]AGGGTGGTTCTCACA	55764
rs757571622	snp	A/C/G			intron-variant	IFT122	GRCh38.p7	3:129486496	GCTGTACTTACTGAC[A/C/G]GACTTTAGAAAGGAA	55764
rs757571749	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129472951	TTTTCCTTTTTATTC[A/G]TTACAAGCGTATTTT	55764
rs757574680	snp	A/G	4.94287e-05	0.00497111	missense	IFT122	GRCh38.p7	3:129483494	CCCCAGGAACCAAAC[A/G]CCAACAGTGTAGCTT	55764
rs757583043	snp	C/T	1.6582e-05	0.00287936	synonymous-codon	IFT122	GRCh38.p7	3:129514404	GAAAATACTCTTCAC[C/T]TTGGCCAAGCAGAGC	55764
rs757604807	in-del	-/C	1.69324e-05	0.00290962	intron-variant	IFT122	GRCh38.p7	3:129488185	GCATCTGGAGGCAGG[-/C]TCTGTATGCATCTGG	55764
rs757623089	in-del	-/T	4.94429e-05	0.00497182	intron-variant	IFT122	GRCh38.p7	3:129506380	CTAAATAGCATGTGC[-/T]TTTTTTCCTCCCTCC	55764
rs757661905	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473754	CTCCCAAATTCTATA[C/T]TCACCCAGCATGATG	55764
rs757709314	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441028	CACCAAACACAAGCT[C/T]TCCTAATTGGGAAGT	55764
rs757709353	snp	C/G	1.64746e-05	0.00287002	intron-variant	IFT122	GRCh38.p7	3:129476658	ACAGTTCTCTCACCC[C/G]GCAGGTGGTCGGCTG	55764
rs757753414	snp	A/G	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129449865	TTTCCCTTGTCTTCT[A/G]TTCAGTATAAATGAC	55764
rs757771646	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458409	CATCTTTGTTTACTC[A/C]GTGTCAGACAAAGCA	55764
rs757783150	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471518	CACACTGCAGTGGGA[A/G]GGAATGGGGTCTTGT	55764
rs757797750	snp	C/T	1.64732e-05	0.0028699	intron-variant	IFT122	GRCh38.p7	3:129449949	ACTGGTAGGATTTTG[C/T]CTTAGTTTCCTCTTA	55764
rs757823317	snp	A/G	0.00354699	0.0419633	intron-variant	IFT122	GRCh38.p7	3:129488404	GCAAAGAAGGTAAGC[A/G]TCTAGCCAGCAGGAG	55764
rs757840525	snp	G/T	1.64852e-05	0.00287094	missense	IFT122	GRCh38.p7	3:129517483	GACGTGCTACACCTG[G/T]TTGAGTTCTACCTGG	55764
rs757855780	snp	C/T	4.94328e-05	0.00497131	intron-variant	IFT122	GRCh38.p7	3:129479944	GCTCCCTCACGTCTC[C/T]TGTCAGGCTGATAAT	55764
rs757909151	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	IFT122	GRCh38.p7	3:129479874	CATCAAGGTGATCGG[C/T]GGCCCTCCTGGAAGA	55764
rs757911332	snp	A/C/T	3.29453e-05	0.00405854	missense, stop-gained, intron-variant	IFT122	GRCh38.p7	3:129492156	GCCTTCATCAGAGTA[A/C/T]AAGACCTCCGATATT	55764
rs757964833	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129514243	CTCACCTCTCACAAG[C/T]GCACAGAGCCTTCCT	55764
rs757965239	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460893	GCACCTCCATCTTCC[A/G]TTTCTGGGCCTCCAC	55764
rs757979000	snp	C/T	6.58979e-05	0.00573974	synonymous-codon, downstream-variant-500B	IFT122	GRCh38.p7	3:129507675	CACAGCAGATCCTGC[C/T]CAGAAGGACACAATG	55764
rs757979995	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129486561	GTTTGAGAAAGCTTC[C/T]AGGAGATGGTGAAAC	55764
rs758020295	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438560	TTGCAGAACAGACAC[A/G]AGAACCCAAGTCTAC	55764
rs758028553	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469360	GGAACGTAATGACAT[C/T]CTGGCTGTGGCTGAC	55764
rs758055867	snp	A/G	3.48943e-05	0.00417683	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476275	AATGGTTATGGATTC[A/G]GAAATGGTTTTTCCC	55764
rs758065976	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473997	GCTAGCCTTCCATGT[C/T]GTGATTCATAAGAAT	55764
rs758067204	snp	C/T	1.65031e-05	0.00287251	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507761	CCATCCATCGCCACA[C/T]GGTAAGGTGGCTGGG	55764
rs758084884	in-del	-/TGTT	0.000164758	0.0090748	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507628	GGCAGCCACAGACAC[-/TGTT]TGACACGTTTCCCCT	55764
rs758118681	in-del	-/ACACACACACACAGAGACTGCCCCC			intron-variant	IFT122	GRCh38.p7	3:129516343	ACAGAGACTGCCCCT[-/ACACACACACACAGAGACTGCCCCC]GCACACACACACAGA	55764
rs758143988	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129478452	TATTTTATTATTTTT[A/T]AAAAAATATTTTTCT	55764
rs758172067	snp	C/T	5.67972e-05	0.00532873	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460983	TTGCTTGAGGCCAAG[C/T]GTTCAAAACCAACCT	55764
rs758174828	snp	A/G/T	6.62168e-05	0.00575366	intron-variant, missense	IFT122	GRCh38.p7	3:129519760	CCTGGTAGCTCACAT[A/G/T]TGCTTCTCTTGGCCA	55764
rs758194778	snp	A/G	0.000147485	0.00858607	missense	IFT122	GRCh38.p7	3:129483626	GTGGTCGGCTACAAT[A/G]GCTCCAAGATCTTCT	55764
rs758202449	snp	C/T	0.000248252	0.0111384	missense	IFT122	GRCh38.p7	3:129514540	ATCCGCGCCAAGCCC[C/T]TCCACGACAGTGAGG	55764
rs758249040	snp	C/T	1.65474e-05	0.00287636	intron-variant	IFT122	GRCh38.p7	3:129502704	TACCTGCCCCTTCCC[C/T]CTCCAGGTTGATCGA	55764
rs758257397	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129466306	GGCCCATGCTGTACC[A/G]TGCATGTCTAATGCT	55764
rs758292604	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481121	GCTATCATGATCACT[A/G]TCATCATTATTATAA	55764
rs758292661	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129478634	TTTTTAGTAGAGACG[C/T]GAGGCTGTACTTTGG	55764
rs758300126	snp	A/G	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129500055	ATCTGTGGTGACCAT[A/G]GCTGGGTTGACATGT	55764
rs758330933	in-del	-/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475336	GCAGTTCCTAAAAAA[-/G]GTTCAACGTAGAGTT	55764
rs758335206	snp	C/T	1.71731e-05	0.00293023	intron-variant	IFT122	GRCh38.p7	3:129488167	CATGGGTAATCATCC[C/T]ACGCATCTGGAGGCA	55764
rs758387321	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450881	GCCTGCCGCTACGCT[C/T]AGCTAATTTTTTGTA	55764
rs758391173	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493678	GGTTTACCTACCCGC[A/G]TGGTAAAGGGCTTGT	55764
rs758404362	snp	A/C/G	6.59419e-05	0.00574172	intron-variant	IFT122	GRCh38.p7	3:129466857	GTGTAGTTCTAGGCA[A/C/G]TGTAATTTTGAACAA	55764
rs758423458	snp	G/T	1.64817e-05	0.00287064	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478134	GGACTTATCAGACAT[G/T]CATTACCGGGTAAAG	55764
rs758425282	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129501023	GTGAGTGTCAGGCTG[G/T]CTTTGCTCTGTGGCT	55764
rs758431632	snp	A/G	1.64757e-05	0.00287012	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504416	GCTTTGAGGAAGCCC[A/G]GAAAGGTAGGCAACA	55764
rs758432144	snp	A/G	1.65504e-05	0.00287662	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478031	TTCGGATTAAATGCA[A/G]AGAGCTTGTCAAGAA	55764
rs758447639	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129502346	TTCTCATCTGAGAGA[C/T]GGAAATAATCATGCC	55764
rs758473452	snp	A/C/G	3.29453e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129506433	AGGCTGGGCGACAGA[A/C/G]AGAAGCGGTCCAGGT	55764
rs758504782	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482976	CAAGTGTGGAAGGGC[A/G]TCTGTGCTGCCCCAT	55764
rs758536388	in-del	-/A	2.3523e-05	0.00342943	frameshift-variant, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439802	GCTCCGCGGTCCCCC[-/A]GACTCAGACTCTCCA	55764
rs758537947	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454697	TATAAGGCCCAGTAG[A/G]TACAGAAGAGCTATT	55764
rs758578382	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129509342	CTGTAGTTGTGAGAG[C/G]ATCAGCTTCGATGAT	55764
rs758581995	snp	C/T	4.94303e-05	0.00497119	intron-variant	IFT122	GRCh38.p7	3:129519058	GGGTGGAGGCTAGGG[C/T]CTGTCTCCATCTCTG	55764
rs758585414	snp	A/G	1.6522e-05	0.00287414	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458549	AATTCTCTCTGGGAA[A/G]TGCTGGTTTAAGATA	55764
rs758586391	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129510233	GCCCAGCCTTCCCGC[C/T]GTTCTTTGACCTCTC	55764
rs758591719	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129469292	CCTTAGAGCTATACT[C/T]ATCAGCAGGCTGTGG	55764
rs758594993	in-del	-/AGA	1.67136e-05	0.00289076	intron-variant	IFT122	GRCh38.p7	3:129461048	AAACAGTGGGTGAGG[-/AGA]AGGAGAATTAATTCT	55764
rs758595682	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129483989	GCCCAGCGTGGGGCC[A/G]AATGGAGTGAGCAGC	55764
rs758635681	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475686	AGGCATGGTGGCACT[C/T]ACCTATGGTCCCAGC	55764
rs758644002	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476446	AGTGCGGCTTGGGAC[C/T]GTTGGGGAGCAGAAC	55764
rs758677168	snp	A/C	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466953	TGTCATTGTCAACAG[A/C]TATATTCAGGAAATC	55764
rs758677272	snp	A/T	1.64814e-05	0.00287061	intron-variant	IFT122	GRCh38.p7	3:129452004	GCGAAGGATGGTAAA[A/T]GGCTGCTCTGGGTTT	55764
rs758681565	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129471031	ATTAAAATATAGAGA[A/G]CATGGTAGTAGGATG	55764
rs758705902	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458538	GTTTTCTAAAGAATT[C/G]TCTCTGGGAAATGCT	55764
rs758713222	snp	A/T	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129519128	AGATTCTGCGGCTAG[A/T]GGAGACCAAGGACTC	55764
rs758730483	snp	C/T	9.69885e-05	0.00696311	intron-variant	IFT122	GRCh38.p7	3:129514269	TTCCTCACGGTCTTT[C/T]CTCTGCCTTCCCGGC	55764
rs758746484	in-del	-/TA	1.79829e-05	0.00299852	frameshift-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520194	TTCCATTCTGAGGAC[-/TA]TGAGTTGCTGGTGCT	55764
rs758776284	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129519083	TCTCTGCTTCTGATT[C/G]CATCCTTGACCAGAT	55764
rs758788927	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129512720	GAAATGGAAGAAGCA[A/C]CAGGCCTTCAGGCTT	55764
rs758790223	snp	A/C/T	3.33824e-05	0.00408538	intron-variant	IFT122	GRCh38.p7	3:129481742	CCTTTGATTAGAGAC[A/C/T]CTCCTCTAGCTTCCC	55764
rs758795660	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129460370	TCCTCAAGGCTCATC[C/T]GTGTTGTAGCATGTG	55764
rs758841413	snp	C/G	1.65693e-05	0.00287826	missense	IFT122	GRCh38.p7	3:129481659	AATGACACTTGCCTG[C/G]TGTATGACATCGACA	55764
rs758844697	snp	A/T	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129514394	TTCACGGCAGGAAAA[A/T]ACTCTTCACCTTGGC	55764
rs758928058	snp	A/G	1.67469e-05	0.00289364	intron-variant	IFT122	GRCh38.p7	3:129463664	GATTTATGTTCCTTC[A/G]TCTTCCACACAGACT	55764
rs758939857	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129492338	CCACAGCCTTGCTCC[G/T]GGGGCAGAGTGGCCA	55764
rs758955252	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129486491	AACAGGCTGTACTTA[A/C]TGACGGACTTTAGAA	55764
rs758955600	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129506260	GGTTATTTAGAGAAG[C/T]GCCATCCCAGCAACG	55764
rs758998922	snp	A/G	1.65367e-05	0.00287543	missense	IFT122	GRCh38.p7	3:129514448	CCTACAGGCTGGCCC[A/G]GCACGCCTATGACAA	55764
rs759016671	in-del	-/CTT	3.29962e-05	0.00406165	intron-variant	IFT122	GRCh38.p7	3:129458686	AGTACACGTAAGTAA[-/CTT]AGGTGTACAGTATTA	55764
rs759026747	snp	A/G	1.64928e-05	0.00287161	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504294	GGGGCAGCTTTATTA[A/G]GACTTCATTTGCTCC	55764
rs759050762	snp	C/T	1.66175e-05	0.00288244	intron-variant	IFT122	GRCh38.p7	3:129476849	ACAGGTGGAAGCAGG[C/T]GGAAAGGGCTGGTGA	55764
rs759062038	snp	C/T	1.65274e-05	0.00287462	missense	IFT122	GRCh38.p7	3:129514505	GATTCCAAAAGTCCA[C/T]TGAGCTGGGTACCCT	55764
rs759076466	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518120	CTGTCCTCTGGGCAA[C/T]TTCATTCTTTGGCAG	55764
rs759107218	snp	A/G	0.000247062	0.0111117	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464753	GGCTCCCTCTCGCCA[A/G]TATGGTCCATCTGCT	55764
rs759143853	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129494214	TTTTTGTTTGTTTGT[G/T]TGTTTTTTTTTTGCA	55764
rs759161612	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129456465	AACACAGTGAAACCT[C/T]GTCTGTACTAAATAT	55764
rs759238858	in-del	-/TTAT			intron-variant	IFT122	GRCh38.p7	3:129511626	CACACAGAAAATTCC[-/TTAT]TTGTCTGCTGAGCTT	55764
rs759240224	snp	A/G	6.58892e-05	0.00573936	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464694	GGATCATCAGCATAC[A/G]GAACAAAAATGGCGA	55764
rs759255347	snp	C/T	1.64735e-05	0.00286993	stop-gained, downstream-variant-500B	IFT122	GRCh38.p7	3:129504379	TACATGCCGTATGCT[C/T]AGTGGCTAGCAGAGA	55764
rs759256225	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129490660	CCCAGAAGCAGAGAA[A/G]TAGGCTCAGAGCGAG	55764
rs759289724	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129482597	ACCTGGCCACCTCTA[G/T]CCCAGAGGTAACTCC	55764
rs759300038	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451918	TCTTTTGCCAGGTTT[A/G]TGACACCTCTGATGG	55764
rs759301393	snp	C/T	0.000148245	0.00860815	intron-variant	IFT122	GRCh38.p7	3:129492135	TTCTTTATTTCTTCG[C/T]CACAGGCCTTCATCA	55764
rs759336961	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511311	TTCTTGGGTTCTTGG[A/G]GCTAACAAAAGGTAT	55764
rs759344980	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129506297	TGCAGATGCTCCAAT[A/G]AGTGTCCTACTTCCA	55764
rs759374444	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	IFT122	GRCh38.p7	3:129517563	GCTGAGACCCAAGCG[A/G]GATGACAGACAGCTA	55764
rs759421550	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129448616	TGAACATACTTGGCC[C/T]CCAGGTAGCCTTTTT	55764
rs759436069	snp	C/T	1.64955e-05	0.00287184	synonymous-codon	IFT122	GRCh38.p7	3:129517470	TCTATGCCCTCCAGA[C/T]GTGCTACACCTGGTT	55764
rs759486076	snp	C/T	1.64868e-05	0.00287109	missense	IFT122	GRCh38.p7	3:129502764	GCGAGCCCCTGCTGC[C/T]GTGCGCTACCTACCT	55764
rs759504657	snp	A/G	4.0184e-05	0.00448223	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520160	TCAGCCTGGTCTTAC[A/G]GCTGTCTTCCCTTAG	55764
rs759514160	snp	C/T	4.94328e-05	0.00497131	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476367	GCATCAGCTACTTTA[C/T]TAAAGGCGAGTACAT	55764
rs759560332	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501309	ATTCTTCTGGAAACA[A/G]CGTTGTGGTCTACAG	55764
rs759561262	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129504875	GGTACCATGAGGACA[A/G]TAAGGGAGGATTGCC	55764
rs759566379	snp	A/T	3.43489e-05	0.00414407	intron-variant	IFT122	GRCh38.p7	3:129488160	CCCCAGGCATGGGTA[A/T]TCATCCCACGCATCT	55764
rs759638911	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129463786	CTCCTCGATGGGAAA[A/G]ACTTGTGCCTTTGAT	55764
rs759640182	snp	C/T	1.64972e-05	0.00287199	intron-variant	IFT122	GRCh38.p7	3:129461210	CTGCATAGTAATCTA[C/T]AGTTGTTTACTTCCC	55764
rs759695434	snp	C/T	1.6476e-05	0.00287014	intron-variant	IFT122	GRCh38.p7	3:129512417	ATCTCTAAAGTGTAT[C/T]CTTTCTCTTATCCCT	55764
rs759740478	in-del	-/TTTA			intron-variant	IFT122	GRCh38.p7	3:129448681	CTTCCAGCTTGCCTT[-/TTTA]TTTATTTATTTATTT	55764
rs759786610	in-del	-/C	1.64749e-05	0.00287005	intron-variant	IFT122	GRCh38.p7	3:129500086	AGGTTTTGGTCCCTG[-/C]CCCGAGAAGCATTTG	55764
rs759786852	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503753	AGAGAAATTTATTAG[A/G]TTTCCCAAGCAGCAT	55764
rs759791482	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473439	TATTGTGAGTAATAT[A/G]TCATAAAGACTCATA	55764
rs759800512	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129503352	CAGTTTTTTCCCTCC[-/C]TTCTCTGCCCCCACC	55764
rs759821230	snp	A/G	6.67564e-05	0.005777	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439835	CCAGTCGTGCCCATC[A/G]AGCAGGGTCCGGCTG	55764
rs759831675	in-del	-/AGC			intron-variant	IFT122	GRCh38.p7	3:129499420	TCAGCCTCACTCTGA[-/AGC]AGCATGTGGTATCAC	55764
rs759841262	snp	G/T	7.27352e-05	0.00603012	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439717	TGAGGCCCAAAAGGG[G/T]ACAGTAACTTACCGG	55764
rs759861376	snp	A/G	1.90387e-05	0.00308529	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520257	TGCAAGGATGACCCT[A/G]GCCCATGACCAGCAT	55764
rs759968201	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453190	TCTAGGGCATAGACG[A/G]GGTATTTGCTTTAGA	55764
rs759975764	snp	A/G	3.27102e-05	0.00404401	intron-variant	IFT122	GRCh38.p7	3:129515479	CGGGAGTCCGTGGCT[A/G]TTTTGTAGGAGTTGG	55764
rs759981362	snp	C/T	6.59033e-05	0.00573997	missense	IFT122	GRCh38.p7	3:129519121	GGCTCCCAGATTCTG[C/T]GGCTAGTGGAGACCA	55764
rs759984088	snp	C/T	1.64732e-05	0.0028699	missense	IFT122	GRCh38.p7	3:129506412	CCACTCCTACAGCGT[C/T]CCACAAGGCTGGGCG	55764
rs760008828	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129478979	TAAGTCAATGCCAAG[A/C]GAAGTTTGGAAAGAC	55764
rs760036661	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129500605	ACCATGGATATCTTC[C/T]CTTAGGAGACACTCT	55764
rs760048530	snp	A/G	1.64768e-05	0.00287021	intron-variant, missense	IFT122	GRCh38.p7	3:129467009	ACAGTAGTCAGGGTA[A/G]TGAGGCAGAGGAGGA	55764
rs760057782	snp	G/T	3.29533e-05	0.00405901	intron-variant	IFT122	GRCh38.p7	3:129519082	ATCTCTGCTTCTGAT[G/T]CCATCCTTGACCAGA	55764
rs760098297	snp	C/T	0.000131952	0.0081215	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129456150	CTTGTTTGGGTCATG[C/T]AGCTGGTCAGTGAGA	55764
rs760119480	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457507	CCATCCATGTGGATG[C/G]GTCTGTCTCCTCTCT	55764
rs760119717	snp	C/T	1.65545e-05	0.00287697	intron-variant	IFT122	GRCh38.p7	3:129481713	AAGTCCCTGAGGGGG[C/T]CCAGGGACATCATCC	55764
rs760143667	in-del	-/AA			downstream-variant-500B	IFT122	GRCh38.p7	3:129520824	GGGATCCATCTTGAC[-/AA]GAGAAAATACGTGGG	55764
rs760157093	snp	A/G	1.69135e-05	0.002908	intron-variant	IFT122	GRCh38.p7	3:129514385	TTAACCCTGTTCACG[A/G]CAGGAAAATACTCTT	55764
rs760157152	snp	A/G	6.6084e-05	0.00574784	missense	IFT122	GRCh38.p7	3:129519605	CAGTGGTGGTGAGCC[A/G]GCTGGTGCTGCGCTC	55764
rs760173190	snp	C/T	3.31466e-05	0.0040709	intron-variant, missense	IFT122	GRCh38.p7	3:129519778	CTTCTCTTGGCCACT[C/T]TTCCCTTGCCCAAAT	55764
rs760182208	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129490840	CTTGGCCCATGTGAT[G/T]CCCGCATTGCCCTTT	55764
rs760196301	snp	C/T	1.64795e-05	0.00287045	intron-variant	IFT122	GRCh38.p7	3:129483479	CCCACTGTCCCTGTT[C/T]CCCAGGAACCAAACG	55764
rs760210062	snp	C/T	3.31225e-05	0.00406941	intron-variant	IFT122	GRCh38.p7	3:129519231	GAGGGCAGCCTCCAT[C/T]CCTTCTCCTGTGCAC	55764
rs760228928	snp	A/G			missense	IFT122	GRCh38.p7	3:129506465	CTGGAGCAGCTCACA[A/G]ACAATGCCGTGGCGG	55764
rs760229757	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129497368	TCTTCGGTTTGCCAA[A/G]CCTCCCTTCCCTTCT	55764
rs760263484	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129518953	CAGAGTCCCTTCCTT[C/G]TGATTCCTTGGCCTG	55764
rs760279668	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445688	GTTGAAATCCTGGCC[C/T]TTGCACTTGCTAGTT	55764
rs760317873	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487384	ATTTGCTGGGACAGG[C/T]CATTTGTCCTCTCTG	55764
rs760380233	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129446988	CTGAACCAATGAAAT[C/G]CTCTGCCTGGGGCAT	55764
rs760391278	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129479388	CAGCAGTGAGCTATG[A/G]TAGCGCCACTACACT	55764
rs760398626	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129511656	GCTTCTGGCAGCCTC[G/T]AGGTACGAAGACCAA	55764
rs760399736	snp	A/G	0.000314291	0.0125318	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504273	AGTGTTTTCATGGGG[A/G]CTGCAGGGGCAGCTT	55764
rs760410345	snp	A/G	3.29484e-05	0.00405871	intron-variant	IFT122	GRCh38.p7	3:129449834	AGACTTCATCATTTT[A/G]GTTCCTAATTGTCTT	55764
rs760412321	snp	A/C	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464675	GCGCTGGGGATGTTC[A/C]ATGGGATCATCAGCA	55764
rs760427333	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476731	AGTCCATGGGCTTTA[C/T]AAGGACCGCTATGCC	55764
rs760438660	in-del	-/TTTTTTTTTTTTT			intron-variant	IFT122	GRCh38.p7	3:129492817	ATGCTTTTTTTTTCT[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT	55764
rs760451564	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129447538	CTCACCCTGCAAAAC[-/AG]AGTCTTGCTGTCACC	55764
rs760457508	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129514145	GCAGGCCCAGAGATG[-/C]TAAGCAAGGTTAAAG	55764
rs760471441	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129487491	TTATAAACCTAAGAA[-/AG]AGAAGTCGTTAGGAA	55764
rs760472881	in-del	-/GTGT			intron-variant	IFT122	GRCh38.p7	3:129494687	CTAGCTGTGCTAAGT[-/GTGT]GTGTGTGTGTGTGTG	55764
rs760479392	in-del	-/G	1.65012e-05	0.00287234	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476801	ATCACTGAGCAGAAA[-/G]GTAAGAGGCAGGTCC	55764
rs760486634	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485370	TCGAAACTCATGACT[A/G]CAAGACTTACTGGGG	55764
rs760491048	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129499672	GCACTGGGGGCCAGC[A/G]TCCCTGATGCTGTCC	55764
rs760610536	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449917	ACTCAACTGATTTTG[C/G]CTGCCGGAAGCAGAT	55764
rs760626904	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129513812	GGGGGCAGCCAACAT[-/C]GGAGGTGACCTGAGA	55764
rs760684054	in-del	-/C	1.65534e-05	0.00287688	intron-variant	IFT122	GRCh38.p7	3:129517448	CTCCAGCCCCCTCAG[-/C]CCTTTCTCTATGCCC	55764
rs760690119	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487406	TCCTCTCTGAGTCTC[A/G]GTCTCCTGGGCTGTA	55764
rs760724709	snp	C/G	3.30617e-05	0.00406568	intron-variant	IFT122	GRCh38.p7	3:129517456	CCCTCAGCCCTTTCT[C/G]TATGCCCTCCAGACG	55764
rs760733132	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456660	CCAGTCGTGGTGACT[C/T]ATGCCTGTAATCACA	55764
rs760740538	snp	C/T	1.64765e-05	0.00287019	intron-variant	IFT122	GRCh38.p7	3:129479931	TGGACAGGTGAGTGC[C/T]CCCTCACGTCTCCTG	55764
rs760747898	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129503127	GCCAGCTCTGCCAGG[C/G]TGGTGACAGGCACCG	55764
rs760754175	snp	G/T	1.65288e-05	0.00287474	missense	IFT122	GRCh38.p7	3:129519724	ACCATGTGCCCCTCC[G/T]GCTTCCAGGTAGGTG	55764
rs760802486	in-del	-/AAAAG			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503993	GTGTCGCCCGCAATT[-/AAAAG]AAATCTGTTTGCAGC	55764
rs760806571	in-del	-/C	1.64754e-05	0.00287009	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504312	CTTCATTTGCTCCTT[-/C]CCCCAGGCCTTTGCT	55764
rs760810819	snp	A/G	6.59196e-05	0.00574068	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507716	TCTACCACTTCCAGC[A/G]TTTGGCAGAGCTGTA	55764
rs760815869	snp	A/G	3.35728e-05	0.00409698	synonymous-codon, intron-variant	IFT122	GRCh38.p7	3:129460959	TAAAGGCCAAGGTGG[A/G]AGGATTGATTGCTTG	55764
rs760841455	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474916	TCCCAGTGCTTTGGG[A/G]GGCAGAGACAGGGAG	55764
rs760870485	snp	A/G	1.66715e-05	0.00288712	intron-variant	IFT122	GRCh38.p7	3:129483695	CAGGTAACTGGGGGT[A/G]CCTGTCCACTCTTAG	55764
rs760917623	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129452158	GGTCATTCAATCTAG[C/T]AAGTATTTATTGAGG	55764
rs761009312	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453281	AATGGAAATTCTCAA[C/T]TCCATTTTTTTTTTC	55764
rs761051369	snp	A/G	4.94181e-05	0.00497057	intron-variant, missense	IFT122	GRCh38.p7	3:129466928	ACAGAGAGAATGAGG[A/G]TGCCGAGGATGTCAT	55764
rs761057537	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129452700	ATTTTGATTCTCAGT[C/G]AAAATGGAACTACTG	55764
rs761076643	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501564	TATAGAAGAGAGCCA[A/G]GCAGATTTAGGGTGC	55764
rs761100826	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	IFT122	GRCh38.p7	3:129520496	CTAAGGAAAAAAATC[-/T]TGTTACTTTCAGAAC	55764
rs761119166	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510024	TCCAGGCAAGGCTTC[A/G]CGCCAGCTTTCCCTG	55764
rs761128170	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129451731	CATAGACCTGGGTCC[C/T]CTACTTCTTGGTTAC	55764
rs761136514	snp	C/T	6.44988e-05	0.00567849	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520146	TGAGCACTAGGGCTT[C/T]AGCCTGGTCTTACAG	55764
rs761139009	snp	C/T	1.85321e-05	0.00304396	intron-variant	IFT122	GRCh38.p7	3:129478262	GCTGAATTCCATTTG[C/T]GCTCCCCCCCCAGTG	55764
rs761141151	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440965	TGAGATCTCGTTTCT[C/G]TAAAACTGGAGATGG	55764
rs761146738	snp	C/G	8.0525e-05	0.00634476	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439706	GGTGGTGAAACTGAG[C/G]CCCAAAAGGGGACAG	55764
rs761164676	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129486326	TGTAACTAGAGCAAC[A/T]CATTTCACTCTTTGG	55764
rs761184330	snp	C/T	1.73078e-05	0.0029417	missense	IFT122	GRCh38.p7	3:129481612	GCTTGGACATGAGTG[C/T]CTCCCGTAAGAAGCT	55764
rs761209129	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509121	TTGTCATGTAAAGTC[C/T]ACTTTTTGTCACACC	55764
rs761243632	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129447016	CATTTGAAAAATCTT[C/T]GTAATATGGCTCTAG	55764
rs761258622	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129494056	TTTTGGATAGGGGAG[A/T]TGTTCTTGTCCTGCT	55764
rs761262414	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451976	CAAAGACACTGTGTA[C/T]TGTGTGGCATATGCG	55764
rs761282246	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503075	GGGCCTTTCCACTTG[C/T]CCCTTCATTCAGTCA	55764
rs761314098	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129508909	CAGCTGCAGGTGTTG[C/G]AGTTTTCGGTGCATC	55764
rs761345225	snp	A/G	1.64743e-05	0.00287	missense	IFT122	GRCh38.p7	3:129495581	CTTGAAATGTACACC[A/G]ACCTCTGCATGTTTG	55764
rs761387212	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129447410	AAAGACCTGGGATCA[A/G]CAGAAAGGAATGTCT	55764
rs761387325	snp	C/T	1.65258e-05	0.00287448	missense	IFT122	GRCh38.p7	3:129514468	GCCTATGACAAGCTG[C/T]GTGGCCTGTACATCC	55764
rs761403319	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129507832	CCGGGCATATCTAAA[A/G]AGCAGCAGACTGGAT	55764
rs761420085	snp	A/G	3.29451e-05	0.00405851	missense	IFT122	GRCh38.p7	3:129506481	ACAATGCCGTGGCGG[A/G]GAGCAGGTTTAATGA	55764
rs761464058	snp	A/G/T	3.30345e-05	0.00406403	missense	IFT122	GRCh38.p7	3:129502859	CTGGTGCAGCTGCAC[A/G/T]TGGAGACCCAGCGCT	55764
rs761475453	snp	C/T			downstream-variant-500B	IFT122	GRCh38.p7	3:129520946	TCCACCTTCCCCAGC[C/T]CCACAGAGCAGCCCC	55764
rs761505271	snp	C/T	4.56798e-05	0.00477889	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520299	CCTGCACCCTCTGCC[C/T]GCCTTGGGGTCTGCT	55764
rs761508374	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482272	AGTCATCCAGCCCTG[C/T]GGCCTGAGGAAGTGT	55764
rs761534617	snp	A/G	9.8837e-05	0.00702914	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476681	GTCGGCTGCCAGGAC[A/G]GCACCATTTCCTTCT	55764
rs761535856	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456842	AATCGCTTGAACCCG[A/G]GAGTCGGAGGTTGCG	55764
rs761551080	snp	C/T	1.64914e-05	0.00287149	intron-variant	IFT122	GRCh38.p7	3:129461333	CCTGATGTCCTGTCC[C/T]GGAATAACTGAAAAT	55764
rs761571922	snp	A/G	1.65455e-05	0.00287619	intron-variant	IFT122	GRCh38.p7	3:129481708	AGGTGAAGTCCCTGA[A/G]GGGGCCCAGGGACAT	55764
rs761594636	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129468635	AAGCGTGAGCCATCA[C/T]GGGCTGCCGCTTTTC	55764
rs761625437	in-del	-/TTGT			intron-variant	IFT122	GRCh38.p7	3:129494695	GCTAAGTGTGTGTGT[-/TTGT]GTGTGTGTGTGTGTT	55764
rs761636238	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129472279	CCACTTTGGCCTTCC[A/G]AGTAGCTGGGACTAC	55764
rs761639294	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129461446	CTGAGGGGAGGCTGA[C/T]AGTTATTCTTTAAAT	55764
rs761640354	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129486050	GGGCTTCTCAAGGCG[C/G]TGGTGACTTCATGTT	55764
rs761695604	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129514776	CACAGCCCCCGGCCC[C/T]GGCCTCAGCCCTCAG	55764
rs761701925	snp	A/G	1.64833e-05	0.00287078	missense	IFT122	GRCh38.p7	3:129502782	GCGCTACCTACCTCA[A/G]GAAGCTGGACAGCCC	55764
rs761710155	in-del	-/G	1.64798e-05	0.00287047	frameshift-variant	IFT122	GRCh38.p7	3:129495508	TGTGTTTTCCTACCA[-/G]GGGAAGTTCCATGAG	55764
rs761730797	in-del	-/ACACAG			intron-variant	IFT122	GRCh38.p7	3:129517297	CACACACACACACAC[-/ACACAG]ACACAGAGACTGCTC	55764
rs761794933	snp	C/T	3.29462e-05	0.00405857	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479836	AAGGAGCGGGAGTGG[C/T]AGATGGAGTCTCTCA	55764
rs761799026	snp	A/G	9.6103e-05	0.00693125	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440401	GGTTCGCGAAGAGCA[A/G]GAGGTCGAGTCCTCG	55764
rs761828582	snp	A/G	1.64749e-05	0.00287005	intron-variant	IFT122	GRCh38.p7	3:129492097	ATCACCCACTTTTGA[A/G]GCCAAGAAGACAGCT	55764
rs761855436	snp	C/T	1.6477e-05	0.00287024	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507646	TTGACACGTTTCCCC[C/T]CCCACCCGCTGCACA	55764
rs761863738	snp	C/T	1.65877e-05	0.00287986	intron-variant	IFT122	GRCh38.p7	3:129517435	TCCTTTGCAAGGCCT[C/T]CAGCCCCCTCAGCCC	55764
rs761878321	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445869	TTCGAAGTACTGTCA[C/T]TGAGAGTGTACTTCC	55764
rs761881670	snp	C/G/T	6.58907e-05	0.00573948	missense	IFT122	GRCh38.p7	3:129488344	ACAGACACTGATTGG[C/G/T]GTGAACTGGCCATGG	55764
rs761897725	snp	A/G			missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504394	CAGTGGCTAGCAGAG[A/G]ACGATCGCTTTGAGG	55764
rs761904566	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129461503	TGACCTTTACTCTGG[C/T]AAGACATCAGAGACT	55764
rs761914288	snp	G/T	1.64757e-05	0.00287012	splice-donor-variant	IFT122	GRCh38.p7	3:129479924	TGAAGAATGGACAGG[G/T]GAGTGCTCCCTCACG	55764
rs761915189	snp	A/G	3.30726e-05	0.00406635	intron-variant, missense	IFT122	GRCh38.p7	3:129467044	CCAGAGGAAGAGGAC[A/G]ACAGTCCCAGGGACG	55764
rs761960888	snp	A/G	1.64754e-05	0.00287009	intron-variant	IFT122	GRCh38.p7	3:129469314	AGGCTGTGGCCCTTC[A/G]TAACCTCTTTTATCT	55764
rs761994381	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129463077	CTGAAAGAATGATAG[A/T]TTCATAGTAAGTTAC	55764
rs761999628	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129450123	TAAACTATCAGATAA[A/G]AACCTGTGAACAATA	55764
rs762005616	snp	A/T	3.29495e-05	0.00405877	synonymous-codon	IFT122	GRCh38.p7	3:129499919	TTTCCTTGGATCTGG[A/T]GACCCCAAAGAAACA	55764
rs762021104	snp	A/T	0.000197684	0.00993996	intron-variant	IFT122	GRCh38.p7	3:129460828	CTCAGCTTTCATTGT[A/T]GTCTAAGGATTTGTC	55764
rs762038858	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485102	CCAGTCCTACTGGAC[A/G]TGTTTGCTGCTTATA	55764
rs762080381	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129490874	ACGAATTCCTCTTCA[-/C]AAACACTTGTTTGCC	55764
rs762086844	snp	A/T	1.64781e-05	0.00287033	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507710	GCAAGTTCTACCACT[A/T]CCAGCGTTTGGCAGA	55764
rs762123045	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129497772	CTGAATTTGAGAAAT[A/G]TGTACCTACACATTA	55764
rs762203286	snp	A/G	3.30557e-05	0.00406531	missense	IFT122	GRCh38.p7	3:129514453	AGGCTGGCCCGGCAC[A/G]CCTATGACAAGCTGC	55764
rs762235183	snp	C/G	1.65179e-05	0.00287379	synonymous-codon	IFT122	GRCh38.p7	3:129519711	TGACGCCTCCATTAC[C/G]ATGTGCCCCTCCTGC	55764
rs762275585	snp	A/G	1.6554e-05	0.00287693	missense	IFT122	GRCh38.p7	3:129483681	CCGTGGAGGTGCCGC[A/G]GGTAACTGGGGGTGC	55764
rs762280545	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487425	TCCTGGGCTGTAGCC[A/G]GGGAGAAATAATACC	55764
rs762286453	snp	C/T	1.65143e-05	0.00287348	missense	IFT122	GRCh38.p7	3:129519623	TGGTGCTGCGCTCCA[C/T]GAGCCGCCGGGATGT	55764
rs762291040	snp	C/T	8.26166e-05	0.00642662	missense, intron-variant	IFT122	GRCh38.p7	3:129460942	GCCACAGATAAAGCA[C/T]CTAAAGGCCAAGGTG	55764
rs762295389	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475275	ATTGGAATCCTCATA[C/G]ACTGCTAATGCAAAT	55764
rs762330027	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129511161	CTTCCTGGATACATG[G/T]CATCTTTCCCAGAGG	55764
rs762356612	in-del	-/GGGTGCCTCTCTGGGTGACCTGCAGGAG	9.89087e-05	0.00703168	intron-variant	IFT122	GRCh38.p7	3:129519191	TGAGCTTTGAGGTGA[-/GGGTGCCTCTCTGGGTGACCTGCAGGAG]GGCAGCCTCCATCCC	55764
rs762380359	snp	C/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464698	CATCAGCATACGGAA[C/G]AAAAATGGCGAGGAG	55764
rs762387549	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129482395	TAGGTGGTCAGGACT[C/G]GTTTTCCAGAGTGAA	55764
rs762403788	snp	G/T	3.45477e-05	0.00415604	intron-variant	IFT122	GRCh38.p7	3:129495407	CTGCTTCCTGCCCAT[G/T]GCTGCAGAGGCCATT	55764
rs762404658	snp	G/T	1.65002e-05	0.00287225	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478082	GATTGGCTATCCAAC[G/T]GCCAGAGAAAATCCT	55764
rs762445636	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129474118	AAATTTGAATGTATT[A/G]AACTTATAATTGCAG	55764
rs762457870	snp	A/G	8.43519e-05	0.00649375	intron-variant	IFT122	GRCh38.p7	3:129477973	TGCCTTGCACCTTAC[A/G]TAACAACCTCTTGCT	55764
rs762468367	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129442931	CTCCCTTATTCTATG[A/C]ACTCCCTAGTTTTCT	55764
rs762472886	snp	G/T	1.64803e-05	0.00287052	intron-variant	IFT122	GRCh38.p7	3:129506377	CTTCCTAAATAGCAT[G/T]TGCTTTTTTCCTCCC	55764
rs762490121	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453992	GATAACATTCTGTAG[C/T]CACTGCCAAGAAGTC	55764
rs762505185	snp	A/C	1.64741e-05	0.00286998	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464767	AATATGGTCCATCTG[A/C]TGGAACCCTTCAAGG	55764
rs762557451	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509055	CAAGTTTGGCTTTGG[A/G]AACTGCTTTGGAGCT	55764
rs762567312	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470299	GATGGAGTCTCACTC[C/T]GTGGCCCAGGCTGGA	55764
rs762587761	snp	A/G	3.29522e-05	0.00405894	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476389	CGAGTACATTTTGCT[A/G]GGGGGTTCAGACAAG	55764
rs762587792	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474772	CTGAGGAAGCACCAT[C/T]AAGAAAGAGAAAAGA	55764
rs762605709	snp	C/G/T	4.94192e-05	0.00497067	intron-variant	IFT122	GRCh38.p7	3:129517627	CAGAGCCTGTGTGTG[C/G/T]GGCTGTGTGAGGGGT	55764
rs762611716	snp	A/G/T			downstream-variant-500B	IFT122	GRCh38.p7	3:129520735	TTGTGTGCTCTTAAC[A/G/T]TTTAATCAAAATGGC	55764
rs762675174	snp	C/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451947	GGCACCTTACTTCAG[C/G]CCCTCAAGGGACACA	55764
rs762730432	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129455233	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAT	55764
rs762766266	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457928	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	55764
rs762811336	snp	C/T	1.64852e-05	0.00287094	intron-variant	IFT122	GRCh38.p7	3:129461224	ACAGTTGTTTACTTC[C/T]CAGGCACAATGATGC	55764
rs762822514	snp	C/T	3.29587e-05	0.00405934	intron-variant	IFT122	GRCh38.p7	3:129512428	GTATCCTTTCTCTTA[C/T]CCCTCCTCCGTCCCA	55764
rs762871363	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481391	TCTTTCTTTTGATGA[A/G]TCCTTTTCCCTGCAC	55764
rs762874935	snp	A/G/T	6.58896e-05	0.00573943	missense	IFT122	GRCh38.p7	3:129512334	CGTTCAGTGTCCATC[A/G/T]TCCTGAAACTCTTTT	55764
rs762887663	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129444105	AGACTGGCTTGTGCA[-/C]CCCCGTGAGTAGGAG	55764
rs762895115	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129497838	TGGCATATTTTTGTT[G/T]ACTTGAAAATTGCTT	55764
rs762903311	snp	C/T			synonymous-codon	IFT122	GRCh38.p7	3:129488319	CTACCAGATTGCTTG[C/T]TTGGGTGTCACAGAC	55764
rs762914062	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129504884	AGGACAATAAGGGAG[A/G]ATTGCCACACAGTGT	55764
rs762945545	snp	C/G/T	6.59569e-05	0.00574236	intron-variant	IFT122	GRCh38.p7	3:129461327	CTGATTCCTGATGTC[C/G/T]TGTCCTGGAATAACT	55764
rs762948237	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129459744	CTCCCTCCCTCCCTT[-/C]CTTCCTTCCTTCCTT	55764
rs762952329	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129516579	CACACACACACACAC[-/AG]AGAGACTGCCCCTGC	55764
rs762956633	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129447139	TTGGCAAGAAGAGTC[A/C]AACTGCAAAATATTT	55764
rs762968249	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476499	CGAAACCGGATTCCA[A/G]CTATGTGGTAAGAAG	55764
rs762980889	snp	C/T	6.7193e-05	0.00579586	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439725	AAAAGGGGACAGTAA[C/T]TTACCGGAGGTCATT	55764
rs763003039	snp	G/T			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507483	CACCATCCTGGAGTG[G/T]CCCTACTCCTAAGCA	55764
rs763043080	snp	A/T	0.000103592	0.00719618	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520280	ACCAGCATCCTGGGG[A/T]CGGCCTGCACCCTCT	55764
rs763043544	in-del	-/CTC			intron-variant	IFT122	GRCh38.p7	3:129509323	GTTCTTCGGCAACTT[-/CTC]CTCCTGTAGTTGTGA	55764
rs763049635	snp	C/G	6.59881e-05	0.00574367	intron-variant	IFT122	GRCh38.p7	3:129479735	CCTTGGGGAGGTCTG[C/G]GGGCACTTATTCTGT	55764
rs763054120	snp	A/C/G	3.29697e-05	0.00406005	missense	IFT122	GRCh38.p7	3:129502776	TGCTGTGCGCTACCT[A/C/G]CCTCAAGAAGCTGGA	55764
rs763108634	snp	C/T	3.29652e-05	0.00405974	intron-variant	IFT122	GRCh38.p7	3:129488230	CTGAAAACAGTCTTC[C/T]TTTTTTCCCTTGATG	55764
rs763131383	snp	A/C	1.64917e-05	0.00287151	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129467031	AGAGGAGGAAGAACC[A/C]GAGGAAGAGGACGAC	55764
rs763142182	snp	C/G	1.64977e-05	0.00287203	missense	IFT122	GRCh38.p7	3:129502847	GACCTCAAGTCCCTG[C/G]TGCAGCTGCACGTGG	55764
rs763144734	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439186	ATAATTTTGAGGAGC[C/T]GGATGGATCTTATGA	55764
rs763174903	snp	C/T	2.22998e-05	0.00333907	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439849	CGAGCAGGGTCCGGC[C/T]GCAGCAACGAGCCCA	55764
rs763191434	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129460075	TGTGGTAAAATATAC[A/G]TGACATAAAATTTAT	55764
rs763216213	snp	A/G	3.7924e-05	0.00435437	missense	IFT122	GRCh38.p7	3:129515587	CCCTTCATCTTCTCC[A/G]CCTCTTCCTACGGTG	55764
rs763232147	snp	C/T	1.64792e-05	0.00287042	intron-variant	IFT122	GRCh38.p7	3:129495621	AGGTAACCTACCCTG[C/T]CCCAGGCCCAAGCTC	55764
rs763244926	snp	C/T	3.8529e-05	0.00438896	intron-variant	IFT122	GRCh38.p7	3:129467118	AGGGCCCAGGCCCCA[C/T]ACAGACTTGCCAGGA	55764
rs763257702	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485079	TGGATGTTCCACAGC[C/T]TTCTTTACCAGTCCT	55764
rs763275725	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129501135	TTCAGCCTTGGGACT[A/C]AGCACACCGGACCTT	55764
rs763319564	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129505592	GAGAACGGAACAAAG[G/T]CCAGACCTTCTCCTT	55764
rs763332787	snp	C/T	3.29571e-05	0.00405924	missense	IFT122	GRCh38.p7	3:129499908	CTTCCTCAGGATTTC[C/T]TTGGATCTGGAGACC	55764
rs763353659	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477906	TTTTTCAATGAGAGT[A/G]TCTCACTTTAATTGC	55764
rs763367383	in-del	-/CCCAGCCCAGA			intron-variant	IFT122	GRCh38.p7	3:129467998	CTCACAGGGACTGAG[-/CCCAGCCCAGA]GCCATATGTGGCCTC	55764
rs763426405	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129443074	ATTTACTGAGTACTT[C/G]CTATAGGCCACATGT	55764
rs763430912	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129477309	TAGTCATTCTAAGCC[C/T]TAAGACTGCAGTCTC	55764
rs763456289	snp	A/T	0.000148318	0.00861028	intron-variant	IFT122	GRCh38.p7	3:129460814	TGGTACATGATTTGC[A/T]CAGCTTTCATTGTTG	55764
rs763504971	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	IFT122	GRCh38.p7	3:129495520	CCAGGGGAAGTTCCA[C/T]GAGGCCGCCAAACTG	55764
rs763542696	snp	C/T	3.35835e-05	0.00409764	missense	IFT122	GRCh38.p7	3:129483587	AGCACCTTCCCTGTG[C/T]ACCGGCAGAAGCTGC	55764
rs763542859	snp	A/G/T	8.23708e-05	0.00641712	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476739	GGCTTTACAAGGACC[A/G/T]CTATGCCTACAGGGA	55764
rs763562701	snp	A/G	8.23744e-05	0.0064172	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507654	TTTCCCCTCCCACCC[A/G]CTGCACACAGCAGAT	55764
rs763595600	snp	A/G	1.6477e-05	0.00287024	synonymous-codon	IFT122	GRCh38.p7	3:129483490	TGTTCCCCAGGAACC[A/G]AACGCCAACAGTGTA	55764
rs763595907	snp	G/T	1.73177e-05	0.00294254	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476281	TATGGATTCGGAAAT[G/T]GTTTTTCCCTTGCTG	55764
rs763644525	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451963	CCCTCAAGGGACACA[A/G]AGACACTGTGTACTG	55764
rs763674354	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445048	CCTGGGTTTGAGGCC[A/G]GATGCAGTGGCTCAC	55764
rs763678728	snp	A/G	1.7443e-05	0.00295317	missense	IFT122	GRCh38.p7	3:129481603	CTGTGCGCTGCTTGG[A/G]CATGAGTGCCTCCCG	55764
rs763706867	snp	C/G	3.45501e-05	0.00415618	intron-variant	IFT122	GRCh38.p7	3:129495409	GCTTCCTGCCCATGG[C/G]TGCAGAGGCCATTTC	55764
rs763715524	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511762	TCCGCATGTGTGCTC[A/G]TTTGGTGGCACATCA	55764
rs763716993	snp	A/G	1.64773e-05	0.00287026	missense	IFT122	GRCh38.p7	3:129517504	TTCTACCTGGAGGAA[A/G]GGATCACTGATGAAG	55764
rs763720740	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129485480	GAAAGCAAGAGGAAG[A/T]AGGGAATGAGGTGGG	55764
rs763727434	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129479462	ATAAATAAATAATCA[A/G]AGTTAGAACTCCAAG	55764
rs763728571	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129449953	GTAGGATTTTGTCTT[A/C]GTTTCCTCTTAAAGT	55764
rs763730562	snp	A/G	1.64762e-05	0.00287016	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464781	GCTGGAACCCTTCAA[A/G]GTACTCTTAAAGTTG	55764
rs763739913	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129518958	TCCCTTCCTTCTGAT[A/T]CCTTGGCCTGAGCCC	55764
rs763749806	snp	A/G	1.64762e-05	0.00287016	intron-variant	IFT122	GRCh38.p7	3:129519095	ATTCCATCCTTGACC[A/G]GATCCCTCCAGGCTC	55764
rs763755540	in-del	-/T			frameshift-variant, intron-variant	IFT122	GRCh38.p7	3:129460886	TTCATTGCACCTCCA[-/T]TCTTCCATTTCTGGG	55764
rs763774981	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129500700	CAGGAAGTACAGCAG[A/G]AACACAGCGAGTTGG	55764
rs763802551	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457789	TGCCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC	55764
rs763854055	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129472171	TTTTATTTACTTTTT[A/G]AGAAAAGGCCTCACC	55764
rs763857485	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129464868	TCCCTACATTCAAAG[C/G]CTTCTCACCTCACTT	55764
rs763872640	snp	C/T	1.6477e-05	0.00287024	intron-variant	IFT122	GRCh38.p7	3:129488236	ACAGTCTTCTTTTTT[C/T]CCCTTGATGAAATCC	55764
rs763905862	snp	A/G	1.64746e-05	0.00287002	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476393	TACATTTTGCTGGGG[A/G]GTTCAGACAAGCAAG	55764
rs763938738	snp	C/T	1.64846e-05	0.0028709	intron-variant	IFT122	GRCh38.p7	3:129461225	CAGTTGTTTACTTCC[C/T]AGGCACAATGATGCT	55764
rs763953848	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129484876	TTTCCCCCAACGGTA[A/C]CAGTGTGCATAGCTC	55764
rs763955211	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487589	ATCAGGAGAGCTGTT[C/T]CCAGAGGCTTCCAGG	55764
rs763970596	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129490844	GCCCATGTGATGCCC[A/G]CATTGCCCTTTTCTA	55764
rs763993447	snp	C/T	0.000124831	0.00789936	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520281	CCAGCATCCTGGGGA[C/T]GGCCTGCACCCTCTG	55764
rs764010474	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129455427	CCGCCCACCTCGGCC[G/T]CCCAAAGTGCTGGGA	55764
rs764022025	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129443368	TGTGTCTTCTGACAG[C/T]GTATCTCTTTTATAA	55764
rs764025106	snp	C/T	9.88761e-05	0.00703052	intron-variant	IFT122	GRCh38.p7	3:129512433	CTTTCTCTTATCCCT[C/T]CTCCGTCCCACCACC	55764
rs764129132	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475048	TAGTCCCAGCTACTG[G/T]GGGTGGTGAGGGGCT	55764
rs764133917	snp	C/T	6.41787e-05	0.00566438	splice-donor-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439729	GGGGACAGTAACTTA[C/T]CGGAGGTCATTCGGC	55764
rs764155396	snp	A/C/T	8.23627e-05	0.0064168	intron-variant, synonymous-codon, stop-gained	IFT122	GRCh38.p7	3:129466956	CATTGTCAACAGATA[A/C/T]ATTCAGGAAATCCCT	55764
rs764163322	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129494321	AAAGTGTAGGGATCA[C/T]AGGTGTAAGCCACCA	55764
rs764168701	in-del	-/TG	3.29468e-05	0.00405861	intron-variant	IFT122	GRCh38.p7	3:129517630	GCCTGTGTGTGCGGC[-/TG]TGTGTGAGGGGTCTG	55764
rs764185924	snp	A/G	1.64762e-05	0.00287016	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507638	GACACTGTTTGACAC[A/G]TTTCCCCTCCCACCC	55764
rs764201815	snp	C/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479830	GGAGTGAAGGAGCGG[C/G]AGTGGCAGATGGAGT	55764
rs764222986	snp	C/T	2.24495e-05	0.00335026	synonymous-codon	IFT122	GRCh38.p7	3:129515514	CTTGTGCTACCGCTG[C/T]TCCACCAACAACCCG	55764
rs764301487	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129503181	GCTCCAGTGCCTGCT[A/G]TTGGGCTGAGCTGCC	55764
rs764349771	snp	A/G	1.65083e-05	0.00287296	intron-variant, missense	IFT122	GRCh38.p7	3:129467038	GAAGAACCAGAGGAA[A/G]AGGACGACAGTCCCA	55764
rs764386518	snp	C/G	8.23879e-05	0.00641772	intron-variant	IFT122	GRCh38.p7	3:129460815	GGTACATGATTTGCT[C/G]AGCTTTCATTGTTGT	55764
rs764393609	snp	A/G	4.94173e-05	0.00497053	missense	IFT122	GRCh38.p7	3:129506505	TTAATGATGCTGCCT[A/G]TTATTACTGGATGCT	55764
rs764405590	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129451353	GTCTTGAACTCCTGG[-/T]TTCAAGCAATCCTCC	55764
rs764418590	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	IFT122	GRCh38.p7	3:129499916	GGATTTCCTTGGATC[C/T]GGAGACCCCAAAGAA	55764
rs764422719	snp	C/G	1.66557e-05	0.00288575	intron-variant	IFT122	GRCh38.p7	3:129519546	GTGAGGACACTGTGC[C/G]TCCTTCCCGCCCACC	55764
rs764512677	snp	C/T	3.3284e-05	0.00407932	missense	IFT122	GRCh38.p7	3:129514397	ACGGCAGGAAAATAC[C/T]CTTCACCTTGGCCAA	55764
rs764513943	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129467469	AATCCTTCGAAGAAC[A/G]TGATTTTTAATGTCT	55764
rs764550583	snp	A/C/T	3.29534e-05	0.00405904	missense, synonymous-codon	IFT122	GRCh38.p7	3:129483493	TCCCCAGGAACCAAA[A/C/T]GCCAACAGTGTAGCT	55764
rs764568165	in-del	-/CTT	1.64841e-05	0.00287085	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504443	AACACAGACTGTCAC[-/CTT]CTAGAAGGAGCAGGA	55764
rs764607453	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129487408	CTCTCTGAGTCTCGG[A/T]CTCCTGGGCTGTAGC	55764
rs764611837	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510030	CAAGGCTTCACGCCA[A/G]CTTTCCCTGACCTGC	55764
rs764639679	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464695	GATCATCAGCATACG[A/G]AACAAAAATGGCGAG	55764
rs764657220	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440971	CTCGTTTCTCTAAAA[C/G]TGGAGATGGGCAGGT	55764
rs764665773	snp	C/T	4.95511e-05	0.00497726	missense	IFT122	GRCh38.p7	3:129519619	CGGCTGGTGCTGCGC[C/T]CCATGAGCCGCCGGG	55764
rs764668446	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129512481	CCAAGAAATTCCTTC[C/T]AGAGCACTTTCCTGG	55764
rs764675179	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129494846	CTCAGCGTCCTTCAC[G/T]CTAACACTTGGGTAG	55764
rs764681135	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473733	CACTTTCCGGGTGCT[A/G]TGGTCCTCCCAAATT	55764
rs764703885	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129509172	TTTTGTTGTTGTTGC[A/C]TAGAATAAGAAAAGA	55764
rs764713297	snp	A/C	1.64727e-05	0.00286986	intron-variant	IFT122	GRCh38.p7	3:129492137	CTTTATTTCTTCGCC[A/C]CAGGCCTTCATCAGA	55764
rs764716919	snp	A/G	1.64735e-05	0.00286993	stop-gained, downstream-variant-500B	IFT122	GRCh38.p7	3:129504383	TGCCGTATGCTCAGT[A/G]GCTAGCAGAGAACGA	55764
rs764733095	snp	G/T	1.6477e-05	0.00287024	intron-variant	IFT122	GRCh38.p7	3:129479940	GAGTGCTCCCTCACG[G/T]CTCCTGTCAGGCTGA	55764
rs764768307	snp	A/T	1.64846e-05	0.0028709	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504299	AGCTTTATTAAGACT[A/T]CATTTGCTCCTTCCC	55764
rs764775080	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481334	CCTCTGATGAACCTC[A/G]CTTCTGGCCTCCTAA	55764
rs764788910	snp	C/T	1.64732e-05	0.0028699	intron-variant	IFT122	GRCh38.p7	3:129449853	CCTAATTGTCTTTTT[C/T]CCTTGTCTTCTGTTC	55764
rs764807161	snp	A/C	1.69229e-05	0.00290881	intron-variant	IFT122	GRCh38.p7	3:129463672	TTCCTTCATCTTCCA[A/C]ACAGACTCTCAAAAT	55764
rs764850419	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129487841	CAGAGGAAGCTGAGA[C/G]TCTTTCCCCTGGGGT	55764
rs764862072	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129467682	TTCTCTTCAGTTGAG[A/T]TTGCCTGTAGGGAAA	55764
rs764871292	snp	C/G	6.75619e-05	0.00581174	intron-variant	IFT122	GRCh38.p7	3:129477967	TTTCTCTGCCTTGCA[C/G]CTTACATAACAACCT	55764
rs764879296	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129507838	ATATCTAAAGAGCAG[C/G]AGACTGGATGGAATG	55764
rs764906962	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129503382	CCCACAACCACTACT[A/T]CTCTCTGGTGTCAGG	55764
rs764955719	in-del	-/A			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438177	AAATCTCTGCACAAC[-/A]AAAAAAGTCAAGCTA	55764
rs764986031	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129452908	AAATTATCAGACTCT[A/G]GATATAATGGGAGGG	55764
rs765046140	snp	A/G	4.98161e-05	0.00499055	intron-variant	IFT122	GRCh38.p7	3:129502666	TACGGCTTGCCGTTG[A/G]CAAGACCCAGAGCCC	55764
rs765048979	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456846	GCTTGAACCCGGGAG[G/T]CGGAGGTTGCGGTGA	55764
rs765051032	snp	A/T	1.74857e-05	0.00295678	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476267	TGTATTGCAATGGTT[A/T]TGGATTCGGAAATGG	55764
rs765091430	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445920	ATTTTTAGATTACTG[A/G]TATAAACCAAAAATA	55764
rs765092253	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129473340	TTCTAACATTTGGGT[C/T]GTCATGGTTCAGTCT	55764
rs765092803	in-del	A/CAGGCTGGGCAGGGTGCTGATTGG			intron-variant	IFT122	GRCh38.p7	3:129488105	ACAGGGTGGGCTGGG[A/CAGGCTGGGCAGGGTGCTGATTGG]CGGCTGCAGGGCTGC	55764
rs765094818	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492687	GTTCTGGAGCAACCC[C/T]TAGCCCTACTGTTTC	55764
rs765103886	snp	G/T	1.86897e-05	0.00305687	intron-variant	IFT122	GRCh38.p7	3:129481511	GTGACTGACACTGTT[G/T]TCGCTGAAATTTTGC	55764
rs765137728	snp	C/T	1.65425e-05	0.00287593	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129519741	CTTCCAGGTAGGTGG[C/T]CACCCTGGTAGCTCA	55764
rs765190529	snp	C/T	1.64982e-05	0.00287208	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507754	TACCATGCCATCCAT[C/T]GCCACACGGTAAGGT	55764
rs765280340	snp	C/T	3.29451e-05	0.00405851	synonymous-codon	IFT122	GRCh38.p7	3:129512332	TCCGTTCAGTGTCCA[C/T]CGTCCTGAAACTCTT	55764
rs765285596	snp	C/T	0.000103212	0.00718298	intron-variant	IFT122	GRCh38.p7	3:129488162	CCAGGCATGGGTAAT[C/T]ATCCCACGCATCTGG	55764
rs765299204	snp	A/C	3.29636e-05	0.00405964	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478128	TTCAGAGGACTTATC[A/C]GACATGCATTACCGG	55764
rs765312898	snp	G/T	1.72826e-05	0.00293956	missense, intron-variant	IFT122	GRCh38.p7	3:129460969	GGTGGGAGGATTGAT[G/T]GCTTGAGGCCAAGCG	55764
rs765320503	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510138	TGATCATAGCTCATG[A/G]CAGCCTCAAACTGCT	55764
rs765326495	snp	A/C	2.76882e-05	0.00372066	synonymous-codon	IFT122	GRCh38.p7	3:129515499	GTAGGAGTTGGTGCC[A/C]TTGTGCTACCGCTGC	55764
rs765347849	snp	C/G	0.000142786	0.00844822	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439719	AGGCCCAAAAGGGGA[C/G]AGTAACTTACCGGAG	55764
rs765355315	snp	C/T	3.2966e-05	0.00405979	intron-variant	IFT122	GRCh38.p7	3:129488228	CTCTGAAAACAGTCT[C/T]CTTTTTTTCCCTTGA	55764
rs765368836	snp	C/T	1.94195e-05	0.00311599	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520166	TGGTCTTACAGCTGT[C/T]TTCCCTTAGATGTTC	55764
rs765392985	snp	A/G	1.6486e-05	0.00287102	intron-variant	IFT122	GRCh38.p7	3:129464816	CCTTCTAGAACAAAC[A/G]CCATCATGAAGAAGG	55764
rs765437372	snp	C/T	1.64925e-05	0.00287158	intron-variant	IFT122	GRCh38.p7	3:129461217	GTAATCTACAGTTGT[C/T]TACTTCCCAGGCACA	55764
rs765459017	snp	A/G	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129506417	CCTACAGCGTTCCAC[A/G]AGGCTGGGCGACAGA	55764
rs765500647	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450194	ACACCCATGAAAGAG[C/T]TGAAAACAATCACAA	55764
rs765510558	in-del	-/A	7.91045e-05	0.00628856	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439709	GTGAAACTGAGGCCC[-/A]AAAAGGGGACAGTAA	55764
rs765510649	snp	A/G	0.000244939	0.0110639	intron-variant	IFT122	GRCh38.p7	3:129515444	CAGGGGGAGGAGGAC[A/G]CGTGCCTGCCCCGGC	55764
rs765521336	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129497806	GGGGGGTGGGGGAGA[G/T]CTAGTCCTGATTAAC	55764
rs765536866	in-del	-/AGAG	8.23608e-05	0.00641667	frameshift-variant	IFT122	GRCh38.p7	3:129506430	ACAAGGCTGGGCGAC[-/AGAG]AGAAGCGGTCCAGGT	55764
rs765538881	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518202	ATCCCCTCAGCCTTA[C/T]AGCCCCCAGAAACAG	55764
rs765551410	snp	A/C	0.000214212	0.010347	intron-variant	IFT122	GRCh38.p7	3:129495624	TAACCTACCCTGTCC[A/C]AGGCCCAAGCTCCAG	55764
rs765560540	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506488	CGTGGCGGAGAGCAG[A/G]TTTAATGATGCTGCC	55764
rs765579421	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129483921	TCCTTGTCCCCTTTC[G/T]GTAGGGATGGGAGGG	55764
rs765588150	snp	C/T	3.29451e-05	0.00405851	intron-variant, missense	IFT122	GRCh38.p7	3:129466946	CCGAGGATGTCATTG[C/T]CAACAGATATATTCA	55764
rs765616156	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474467	GGGGCAGACCTGATT[A/G]ACCCTGTGTCTACAG	55764
rs765647658	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441077	GGAATGACTTTGTCA[C/T]CTTTTGATTCAGTTA	55764
rs765657764	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453737	TGGTGTTGAAGGATT[A/G]TTACAGTTGGGGTAC	55764
rs765661439	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475522	CCAGGCGTGTTCTCA[A/C]ACATCTGTAGTCCCA	55764
rs765685996	snp	C/T	1.66796e-05	0.00288782	intron-variant	IFT122	GRCh38.p7	3:129519540	GGCTGAGTGAGGACA[C/T]TGTGCCTCCTTCCCG	55764
rs765700460	in-del	-/C	6.64905e-05	0.00576548	intron-variant	IFT122	GRCh38.p7	3:129519556	TGTGCCTCCTTCCCG[-/C]CCACCCTGCAGCAAG	55764
rs765747632	snp	G/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129442042	TTTTACCAGAAGCTA[G/T]GAATCTGGGTTTTTA	55764
rs765774680	snp	C/T	1.65718e-05	0.00287848	intron-variant	IFT122	GRCh38.p7	3:129481721	GAGGGGGCCCAGGGA[C/T]ATCATCCTTTGATTA	55764
rs765777740	snp	C/G/T	0.000148264	0.00860893	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476738	GGGCTTTACAAGGAC[C/G/T]GCTATGCCTACAGGG	55764
rs765812976	in-del	-/ATT			intron-variant	IFT122	GRCh38.p7	3:129452895	AGGAGGTGATGAGAA[-/ATT]ATCAGACTCTGGATA	55764
rs765843525	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468951	TTTGTGCTGCAAGAG[A/G]TGTTTCTCTGCCATC	55764
rs765879580	snp	C/T	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129488363	AACTGGCCATGGAAG[C/T]GCTAGAAGGTTTAGA	55764
rs765902102	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129492308	ACAGAGCTCACTGGC[A/G]TCTGGGCATCTGGGC	55764
rs765905838	snp	C/T	1.68258e-05	0.00290045	intron-variant	IFT122	GRCh38.p7	3:129463496	GTTTCAATTATTTGT[C/T]CCTTTTTATTGCTGG	55764
rs765915323	snp	A/G	0.000607605	0.0174193	missense	IFT122	GRCh38.p7	3:129514390	CCTGTTCACGGCAGG[A/G]AAATACTCTTCACCT	55764
rs765940823	snp	A/C	6.58968e-05	0.00573969	intron-variant	IFT122	GRCh38.p7	3:129476615	ACAAATGGGGGAATG[A/C]AGACTTTCTCCAGAG	55764
rs765958794	in-del	-/G	2.03242e-05	0.00318774	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520275	CATGACCAGCATCCT[-/G]GGGGACGGCCTGCAC	55764
rs765969505	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454003	GTAGCCACTGCCAAG[A/G]AGTCACAAAATTGTA	55764
rs765976877	snp	C/T	8.26863e-05	0.00642933	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504277	TTTTCATGGGGGCTG[C/T]AGGGGCAGCTTTATT	55764
rs765993684	snp	C/T	1.66527e-05	0.00288549	intron-variant	IFT122	GRCh38.p7	3:129463646	GTGCAGCTCTGACGA[C/T]AAGATTTATGTTCCT	55764
rs766013948	snp	C/T	1.64789e-05	0.0028704	intron-variant	IFT122	GRCh38.p7	3:129483480	CCACTGTCCCTGTTC[C/T]CCAGGAACCAAACGC	55764
rs766056742	in-del	-/CTTTT			intron-variant	IFT122	GRCh38.p7	3:129468344	CAAGGGCTAGGAATG[-/CTTTT]CTTTTTTTTTTTTGT	55764
rs766058575	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440581	AAAGGGAGGTGCCGC[A/G]CCTGAGGTGGTGGCG	55764
rs766066989	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129487593	GGAGAGCTGTTTCCA[C/G]AGGCTTCCAGGGTAA	55764
rs766105375	snp	G/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449920	CAACTGATTTTGGCT[G/T]CCGGAAGCAGATTAC	55764
rs766152097	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129496634	GTGTGTTTGGTGGCC[-/T]TGTGATGTTGCCCAG	55764
rs766159836	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129495623	GTAACCTACCCTGTC[C/G]CAGGCCCAAGCTCCA	55764
rs766186054	snp	C/G	4.94515e-05	0.00497225	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507727	CAGCGTTTGGCAGAG[C/G]TGTACCATGGTTACC	55764
rs766189629	snp	C/T	1.64738e-05	0.00286995	intron-variant	IFT122	GRCh38.p7	3:129449839	TCATCATTTTGGTTC[C/T]TAATTGTCTTTTTCC	55764
rs766239919	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129446084	ATTAACATCAACACA[C/G]ACTTTAAGTATGATA	55764
rs766243361	snp	C/T	1.65091e-05	0.00287303	intron-variant	IFT122	GRCh38.p7	3:129517463	CCCTTTCTCTATGCC[C/T]TCCAGACGTGCTACA	55764
rs766265056	snp	C/T	1.83839e-05	0.00303176	intron-variant	IFT122	GRCh38.p7	3:129515608	TCCTACGGTGAGTCC[C/T]TGCATCCTGAGCATG	55764
rs766274915	snp	C/T	3.29533e-05	0.00405901	intron-variant	IFT122	GRCh38.p7	3:129479932	GGACAGGTGAGTGCT[C/T]CCTCACGTCTCCTGT	55764
rs766295275	snp	A/C	3.29468e-05	0.00405861	missense	IFT122	GRCh38.p7	3:129479854	ATGGAGTCTCTCATT[A/C]GTTACATCAAGGTGA	55764
rs766305132	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129504891	TAAGGGAGGATTGCC[A/G]CACAGTGTGAGGCAT	55764
rs766326617	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129467837	CCCTGAGGTCATGGG[G/T]GCTGGGAAGTGGGGA	55764
rs766330462	in-del	-/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475344	TAAAAAAGGTTCAAC[-/G]TAGAGTTTAAAAATA	55764
rs766338260	snp	C/G			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504488	AAGACATACATTTCA[C/G]GAAGGCTACCAAGCC	55764
rs766351058	snp	C/T	4.94287e-05	0.00497111	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507653	GTTTCCCCTCCCACC[C/T]GCTGCACACAGCAGA	55764
rs766370204	snp	C/T	1.64732e-05	0.0028699	missense, intron-variant	IFT122	GRCh38.p7	3:129460868	GATCTTGGTCTGTGA[C/T]GTCTTCATTGCACCT	55764
rs766401241	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481213	AGATCTCTGCTAGGT[A/G]GCATCTCCTAAAGCT	55764
rs766404479	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450352	CTAAACAGTTCCATA[C/T]GGATGTTGTCCTATT	55764
rs766412502	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512462	CCGTTCTTGTCTAAT[A/G]GCCCCAAGAAATTCC	55764
rs766428200	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129503487	TTCTATGGCTCAACC[C/G]CCACCCTCCAGCTCA	55764
rs766429633	snp	A/C/G	3.3016e-05	0.00406289	missense	IFT122	GRCh38.p7	3:129519632	GCTCCATGAGCCGCC[A/C/G]GGATGTCCTCATCAA	55764
rs766439305	snp	C/T	1.9374e-05	0.00311234	missense	IFT122	GRCh38.p7	3:129483615	TGCAGGGCTTTGTGG[C/T]CGGCTACAATGGCTC	55764
rs766511106	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516222	GAGACTGCCTCTGCA[-/CA]CACACACAGACTGCC	55764
rs766527872	snp	C/T	5.31816e-05	0.00515635	intron-variant	IFT122	GRCh38.p7	3:129483698	GTAACTGGGGGTGCC[C/T]GTCCACTCTTAGCAC	55764
rs766561355	snp	A/G	6.70747e-05	0.00579076	intron-variant	IFT122	GRCh38.p7	3:129477999	TTGCTAGAACTAGAT[A/G]TTTTTTTCTTTGACA	55764
rs766600664	snp	G/T	1.64827e-05	0.00287073	intron-variant	IFT122	GRCh38.p7	3:129469444	TGTACAAATCCAATT[G/T]CAGTCATGCCTGTTA	55764
rs766628113	snp	A/G	6.65701e-05	0.00576894	intron-variant	IFT122	GRCh38.p7	3:129476840	GGAAGAGGGACAGGT[A/G]GAAGCAGGTGGAAAG	55764
rs766632887	snp	C/T	1.65329e-05	0.0028751	synonymous-codon	IFT122	GRCh38.p7	3:129519729	GTGCCCCTCCTGCTT[C/T]CAGGTAGGTGGCCAC	55764
rs766636275	snp	A/G	1.66891e-05	0.00288864	missense	IFT122	GRCh38.p7	3:129495446	TTCTAATTTTTCCAG[A/G]AGAGGAAGAAGCGGG	55764
rs766644614	snp	G/T	3.29641e-05	0.00405968	intron-variant	IFT122	GRCh38.p7	3:129464794	AAGGTACTCTTAAAG[G/T]TGTCCTCCTTCTAGA	55764
rs766663236	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129477496	TTTGGTCCCCCTGGG[G/T]GACCCTATCTTTTTG	55764
rs766674446	in-del	-/AGGAGAATTAATTCTTTAGGAGT	1.67351e-05	0.00289263	intron-variant	IFT122	GRCh38.p7	3:129461051	CAGTGGGTGAGGAGA[-/AGGAGAATTAATTCTTTAGGAGT]AGGAGAATTAATTTC	55764
rs766675538	snp	A/G	7.75885e-05	0.00622802	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439711	TGAAACTGAGGCCCA[A/G]AAGGGGACAGTAACT	55764
rs766681434	snp	A/G	1.64838e-05	0.00287083	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478118	ATGAGTTGTATTCAG[A/G]GGACTTATCAGACAT	55764
rs766687299	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129506660	GGCTTGTTTATTGGG[C/T]GTATTGTCCATAAGC	55764
rs766701909	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129519096	TTCCATCCTTGACCA[C/G]ATCCCTCCAGGCTCC	55764
rs766718374	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129462008	ATGAAGTCACTAGAT[G/T]AGGAGTCAGAGGCCT	55764
rs766752748	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129450404	AAGCTCCCTCTGGAA[-/C]CTATCCAGGTATATA	55764
rs766762179	in-del	-/T	3.3425e-05	0.00408795	intron-variant	IFT122	GRCh38.p7	3:129478007	CTAGATATTTTTTTC[-/T]TTTGACAGTTCGGAT	55764
rs766830993	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477934	TGCCAGTAGCGCTAA[A/G]TAAATGATGGCTTTT	55764
rs766835006	snp	C/T	1.64743e-05	0.00287	missense	IFT122	GRCh38.p7	3:129506409	CCACCACTCCTACAG[C/T]GTTCCACAAGGCTGG	55764
rs766843185	snp	A/G	4.9423e-05	0.00497082	synonymous-codon	IFT122	GRCh38.p7	3:129495535	TGAGGCCGCCAAACT[A/G]TACAAGAGGAGTGGG	55764
rs766892145	snp	C/G	4.98625e-05	0.00499287	intron-variant	IFT122	GRCh38.p7	3:129514592	CAGGTGGCTTCTCCT[C/G]TCCCTTGAGGCCATC	55764
rs766923060	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129463466	AATCCTGGAGATCCA[C/T]CTAAGTTGTTGTATG	55764
rs766956525	snp	C/T	1.64749e-05	0.00287005	missense	IFT122	GRCh38.p7	3:129495585	AAATGTACACCGACC[C/T]CTGCATGTTTGAGTA	55764
rs766979492	snp	A/G	3.29457e-05	0.00405854	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476420	CAAGTATCTCTTTTC[A/G]CCAAGGATGGAGTGC	55764
rs766988999	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129518124	CCTCTGGGCAACTTC[A/T]TTCTTTGGCAGCCCC	55764
rs767085658	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	IFT122	GRCh38.p7	3:129519108	CCAGATCCCTCCAGG[C/T]TCCCAGATTCTGCGG	55764
rs767099041	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129443315	GTCAGAGGACAATTT[G/T]CAGGATTCCTCTGTA	55764
rs767208488	snp	C/T	0.000131826	0.00811762	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461254	CTATACAATGTGTCT[C/T]CTACAATCCTATTAC	55764
rs767210734	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129490719	CTTGGCCACTGTGCT[C/G]GGCTTTGCAGGGTTG	55764
rs767212265	snp	G/T	1.64746e-05	0.00287002	intron-variant	IFT122	GRCh38.p7	3:129476529	GAGAAAGTTTGTTCT[G/T]TGGGGCCATGGCTTG	55764
rs767255243	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511572	TACAGTGTGCCAGAT[A/G]CCTTCAAAATAAGGT	55764
rs767283750	snp	A/T	1.66145e-05	0.00288218	intron-variant	IFT122	GRCh38.p7	3:129463640	AGGTAAGTGCAGCTC[A/T]GACGATAAGATTTAT	55764
rs767287108	snp	A/C	4.57226e-05	0.00478113	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439869	CAACGAGCCCAGCGC[A/C]GCAACGCCCAGGGTG	55764
rs767300559	snp	C/G			missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478193	ACCTCCTGGTGGTGT[C/G]TGCCAATCACATCAT	55764
rs767312059	snp	A/G	5.58321e-05	0.00528327	splice-donor-variant	IFT122	GRCh38.p7	3:129515600	CCGCCTCTTCCTACG[A/G]TGAGTCCCTGCATCC	55764
rs767319690	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482660	GAGTAGAATGGTTTC[A/G]GGGAAAGAGAGGGCA	55764
rs767335030	snp	G/T	1.64936e-05	0.00287168	intron-variant	IFT122	GRCh38.p7	3:129461342	CTGTCCTGGAATAAC[G/T]GAAAATCTGGGCTAA	55764
rs767352808	in-del	-/TG			frameshift-variant	IFT122	GRCh38.p7	3:129502734	ACATCGCCCGCAAAC[-/TG]GACAAGGCTGAGCGC	55764
rs767393544	snp	C/G	1.64743e-05	0.00287	intron-variant	IFT122	GRCh38.p7	3:129449828	ATTAGCAGACTTCAT[C/G]ATTTTGGTTCCTAAT	55764
rs767401383	snp	A/G	1.64933e-05	0.00287165	utr-variant-3-prime	IFT122	GRCh38.p7	3:129520300	CTGCACCCTCTGCCC[A/G]CCTTGGGGTCTGCTG	55764
rs767453364	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129454244	CAATTGGCCAGGCAC[A/G]GTGGCTCATGCCTAT	55764
rs767457816	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470601	TTTGAGACAGAGTCT[C/T]ACTCTGTCGCCTAGG	55764
rs767468377	snp	A/G	3.29478e-05	0.00405867	intron-variant	IFT122	GRCh38.p7	3:129488246	TTTTTTCCCTTGATG[A/G]AATCCTGCAGTCCGC	55764
rs767491295	snp	A/G	0.000124203	0.00787947	missense	IFT122	GRCh38.p7	3:129515525	GCTGCTCCACCAACA[A/G]CCCGCTGCTCAACAA	55764
rs767500079	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129501455	CCTTGATGGATGTCC[G/T]ACCACCCCATCTTTT	55764
rs767501130	snp	A/G/T	0.00185869	0.0304288	missense	IFT122	GRCh38.p7	3:129479839	GAGCGGGAGTGGCAG[A/G/T]TGGAGTCTCTCATTC	55764
rs767501984	snp	C/G/T	3.30919e-05	0.00406756	intron-variant, missense, synonymous-codon	IFT122	GRCh38.p7	3:129467046	AGAGGAAGAGGACGA[C/G/T]AGTCCCAGGGACGAC	55764
rs767505501	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129506306	TCCAATGAGTGTCCT[A/G]CTTCCAAAGCAGCCC	55764
rs767510838	in-del	-/TA	1.65233e-05	0.00287426	intron-variant	IFT122	GRCh38.p7	3:129458702	TTAGGTGTACAGTAT[-/TA]TGAGTTTGATGCTTA	55764
rs767539606	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439464	ATGACTTCCTAGGAT[C/T]CTCCAACCCCAAGGG	55764
rs767555500	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473543	GGGCTCAAAATCAAA[A/G]CTCCATGTTTTCAGT	55764
rs767568046	snp	C/G	1.648e-05	0.0028705	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507714	GTTCTACCACTTCCA[C/G]CGTTTGGCAGAGCTG	55764
rs767568235	snp	A/G	1.64741e-05	0.00286998	missense	IFT122	GRCh38.p7	3:129499927	GATCTGGAGACCCCA[A/G]AGAAACAAAGATGCT	55764
rs767609724	snp	C/T	3.29478e-05	0.00405867	intron-variant	IFT122	GRCh38.p7	3:129469332	ACCTCTTTTATCTTC[C/T]GTTGATTAGAGAGGA	55764
rs767621103	snp	A/C/T	6.5906e-05	0.00574016	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507647	TGACACGTTTCCCCT[A/C/T]CCACCCGCTGCACAC	55764
rs767655853	snp	A/C	3.29462e-05	0.00405857	synonymous-codon	IFT122	GRCh38.p7	3:129500027	AGCAGGAGAGCACGT[A/C]AAGGCCATCGAGATC	55764
rs767668654	in-del	-/T	1.64779e-05	0.00287031	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479773	CCATGCAGAGCTGGG[-/T]TTGCTTCCTAGGAGA	55764
rs767710310	snp	A/G	1.64765e-05	0.00287019	missense	IFT122	GRCh38.p7	3:129483503	CCAAACGCCAACAGT[A/G]TAGCTTGGAACACCC	55764
rs767732246	snp	A/G	1.64757e-05	0.00287012	intron-variant	IFT122	GRCh38.p7	3:129479927	AGAATGGACAGGTGA[A/G]TGCTCCCTCACGTCT	55764
rs767733663	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129512645	GCTGAACCCAGCAGT[G/T]GGTCTCTGGCCAACA	55764
rs767739383	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129463663	AGATTTATGTTCCTT[A/C]ATCTTCCACACAGAC	55764
rs767741220	snp	A/G	3.37422e-05	0.0041073	intron-variant	IFT122	GRCh38.p7	3:129477975	CCTTGCACCTTACAT[A/G]ACAACCTCTTGCTAG	55764
rs767761037	in-del	-/G	1.65419e-05	0.00287588	frameshift-variant	IFT122	GRCh38.p7	3:129502870	GCACGTGGAGACCCA[-/G]CGCTGGGATGAGGTG	55764
rs767764384	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129450622	AAACAATCCAAACTC[-/T]TATTAGTTTTTCTAC	55764
rs767794799	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129480152	CAGAGTTGAGCTATA[A/G]CCTTTGGCTACATGT	55764
rs767825110	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508244	GAAACCCAAGTAGTT[C/T]TTTTTAGTCACTCCC	55764
rs767833675	snp	A/C/G	9.91583e-05	0.00704066	missense	IFT122	GRCh38.p7	3:129514454	GGCTGGCCCGGCACG[A/C/G]CTATGACAAGCTGCG	55764
rs767863298	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457974	CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC	55764
rs767883700	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129450030	TTTTTTTTTTTTGAG[A/G]TTAAAAAGGCAAGGG	55764
rs767927606	snp	C/G/T	6.58972e-05	0.00573976	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504320	GCTCCTTCCCCCAGG[C/G/T]CTTTGCTTTGGGTGA	55764
rs767945902	snp	A/G	1.64795e-05	0.00287045	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476766	GGGATAGCATGACTG[A/G]CGTCATTGTGCAGCA	55764
rs767950983	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129500617	TTCTCTTAGGAGACA[C/G]TCTTTCCATGAAGGG	55764
rs768040920	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129501414	CCATATATTAATAAT[G/T]GGTGTGTGGGCCCCT	55764
rs768050674	snp	A/T	1.72403e-05	0.00293596	intron-variant	IFT122	GRCh38.p7	3:129478251	GAAGGAGTTGGGCTG[A/T]ATTCCATTTGTGCTC	55764
rs768057751	snp	A/G	0.000115619	0.00760239	missense	IFT122	GRCh38.p7	3:129519712	GACGCCTCCATTACC[A/G]TGTGCCCCTCCTGCT	55764
rs768080950	in-del	-/GCTG			intron-variant	IFT122	GRCh38.p7	3:129487372	TATTGCCAGCTATTT[-/GCTG]GCTGGGACAGGTCAT	55764
rs768096913	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485230	TGCTGGGTCAAAGCA[C/T]GTGTACCTTTGAAAG	55764
rs768097223	snp	C/T	1.64815e-05	0.00287063	intron-variant	IFT122	GRCh38.p7	3:129506380	CCTAAATAGCATGTG[C/T]TTTTTTCCTCCCTCC	55764
rs768122676	snp	A/G			downstream-variant-500B	IFT122	GRCh38.p7	3:129520825	GGATCCATCTTGACA[A/G]GAGAAAATACGTGGG	55764
rs768137168	snp	A/T			missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520246	ACTGCCGCAGGTGCA[A/T]GGATGACCCTGGCCC	55764
rs768160274	snp	A/G	1.64754e-05	0.00287009	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479790	TGCTTCCTAGGAGAA[A/G]CGGCTGCAGTGCCTG	55764
rs768160371	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129485685	CCTGACCTCAAAAAT[-/A]AATGCAGTTTGCTGC	55764
rs768190245	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464704	CATACGGAACAAAAA[C/T]GGCGAGGAGAAAGTA	55764
rs768298529	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473951	TGGGAAGATTGGTCC[A/G]ATGGGAACTAGTGAG	55764
rs768326564	snp	C/T	3.07981e-05	0.00392404	intron-variant	IFT122	GRCh38.p7	3:129514342	CAGGCAGTGCCAGCT[C/T]CTGGGCCTGGTGTTG	55764
rs768367074	snp	C/T	1.65356e-05	0.00287533	intron-variant	IFT122	GRCh38.p7	3:129499863	CGCTGGCACAGGAAG[C/T]TCTGATCCAGAGTGT	55764
rs768377246	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439094	AGAGATCATTTAACC[C/T]AAGTTCTTTTCTACA	55764
rs768379480	snp	A/G	3.29685e-05	0.00405995	synonymous-codon	IFT122	GRCh38.p7	3:129519186	TAAGCTGAGCTTTGA[A/G]GTGAGGGTGCCTCTC	55764
rs768395548	in-del	-/ACAG			intron-variant	IFT122	GRCh38.p7	3:129517303	CACACACACACACAG[-/ACAG]AGACTGCTCCTGCAC	55764
rs768416650	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476504	CCGGATTCCAACTAT[A/G]TGGTAAGAAGAGAAA	55764
rs768426996	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516124	CACAGACTGCCCCTG[-/CA]CACACAGAGACTGCC	55764
rs768443169	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129517966	ACTCAAGTCACTTTC[A/G]CATGCAAGTGACAGA	55764
rs768470050	snp	C/G	4.95471e-05	0.00497705	missense	IFT122	GRCh38.p7	3:129481683	ATCGACACCAAGGAG[C/G]TGCTTTTTCAGGTGA	55764
rs768487219	snp	C/G/T	0.000198398	0.00995826	missense, synonymous-codon	IFT122	GRCh38.p7	3:129519585	AGGTGGCTCAGAGTT[C/G/T]GTGCCAGTGGTGGTG	55764
rs768492829	snp	A/G	4.95675e-05	0.00497808	intron-variant	IFT122	GRCh38.p7	3:129452035	CCATTCTCTATAATA[A/G]CCTCATCATTGTTCA	55764
rs768511401	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509701	TATTCTACTATCAAA[C/T]AGCAAATTCCAGAGC	55764
rs768540910	in-del	-/T	1.64754e-05	0.00287009	intron-variant	IFT122	GRCh38.p7	3:129492246	TACTTGGGGTTCCTG[-/T]TTTAGGGGCAGCCCT	55764
rs768555543	snp	A/G	1.64727e-05	0.00286986	intron-variant	IFT122	GRCh38.p7	3:129464625	TGCCTTTTGTTGGTT[A/G]TGTACACAGCTGGAC	55764
rs768569974	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451154	CCCAAGCTGGTGTGC[A/G]GTAGTGCAGTCATAG	55764
rs768575196	snp	C/T	1.65304e-05	0.00287488	missense	IFT122	GRCh38.p7	3:129514427	AGCAGAGCAAGGCCC[C/T]CGGTGCCTACAGGCT	55764
rs768601369	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508756	CCTGCAAAAAGTTGT[C/T]GAGATGGTTGAAGAA	55764
rs768614110	in-del	-/T	1.65034e-05	0.00287253	splice-donor-variant	IFT122	GRCh38.p7	3:129476801	TCACTGAGCAGAAAG[-/T]GTAAGAGGCAGGTCC	55764
rs768644199	snp	A/G	8.23635e-05	0.00641677	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476678	GTGGTCGGCTGCCAG[A/G]ACGGCACCATTTCCT	55764
rs768644722	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129473106	AGGAGTTCAAGACTA[C/G]CCTGGGCTACATAGA	55764
rs768693229	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487992	GTGACATCCTATGGC[A/G]AGGCAGGCCTGTAGG	55764
rs768718379	snp	A/G	9.56892e-05	0.00691632	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440377	CCGAGCACTGGTGAG[A/G]AGCGGGGCGGTTCGC	55764
rs768725283	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486898	CCTGCTCCGTAGCCT[A/G]TGCCTGCTGCCCCGC	55764
rs768782991	snp	C/T	0.00021418	0.0103462	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476374	CTACTTTACTAAAGG[C/T]GAGTACATTTTGCTG	55764
rs768783466	snp	G/T			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507324	GGTGTCTGCCTGCCT[G/T]TGTCCCAGCAGGCTC	55764
rs768799179	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454823	GTAGTGGCATTTGCA[C/T]AGCACTTTGCAGAGT	55764
rs768801468	in-del	-/TCT			intron-variant	IFT122	GRCh38.p7	3:129488225	TGGCTCTGAAAACAG[-/TCT]TCTTTTTTTCCCTTG	55764
rs768804531	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484823	ACTCACATAAATTGT[A/G]GGAAATAATACAGAG	55764
rs768806088	snp	A/G	1.64901e-05	0.00287137	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129463599	CTGTCTCCAAACACA[A/G]ATCAAGCAGCAAGAT	55764
rs768812229	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129442873	TATACTTTTAGGTTG[A/C]GCTGAAAACTCTATT	55764
rs768818809	snp	G/T	1.64746e-05	0.00287002	missense	IFT122	GRCh38.p7	3:129479903	GAGAAGGCCTCTTAG[G/T]GGGGCTGAAGAATGG	55764
rs768821251	snp	A/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449897	TCGCATTTAAGCCTG[A/T]TGGAACTCAACTGAT	55764
rs768821659	snp	C/T	3.33195e-05	0.0040815	intron-variant	IFT122	GRCh38.p7	3:129488433	AGCTGGAGTTTGGTC[C/T]TTGTGGGGTCCCTTA	55764
rs768876843	snp	C/G	1.7029e-05	0.00291791	intron-variant	IFT122	GRCh38.p7	3:129502920	GGGCTGGGGCCCCAC[C/G]TGAGCCCTGGGACAC	55764
rs768877140	snp	C/T	1.8902e-05	0.00307419	synonymous-codon	IFT122	GRCh38.p7	3:129515589	CTTCATCTTCTCCGC[C/T]TCTTCCTACGGTGAG	55764
rs768903491	in-del	-/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458425	GTGTCAGACAAAGCA[-/G]GTTTGGAACCCAAAT	55764
rs768950676	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448382	TGGTGTCTGATTTAC[A/G]TAGGGCACAAAAGAT	55764
rs769000021	snp	A/G	3.32154e-05	0.00407512	intron-variant	IFT122	GRCh38.p7	3:129507812	CATCTCCTGAGCTAG[A/G]GGTCCCGGGCATATC	55764
rs769014449	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469399	GAAAGTTTCCTTCTA[C/T]CAGCTGAGTGGAAAA	55764
rs769028989	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482225	GAATGCGAAGTGCTT[A/G]GATCTTTGGGGTTGT	55764
rs769054292	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	IFT122	GRCh38.p7	3:129492186	TTAGAGCTCATCAGC[A/G]GCATTGAGGTAAAAG	55764
rs769134531	snp	A/G	0.000103667	0.00719881	intron-variant	IFT122	GRCh38.p7	3:129461030	CCATCTCTACAAATA[A/G]GAAAACAGTGGGTGA	55764
rs769137276	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129459433	TAGCTGGGACTATAG[A/G]CGCTCACCACCATGC	55764
rs769193424	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468511	CACCACGCCGAACTA[A/G]TTTTGCATTTTCAGT	55764
rs769220816	snp	C/T	1.64798e-05	0.00287047	missense, intron-variant	IFT122	GRCh38.p7	3:129460925	AAACAGTAAGAGTAA[C/T]AGCCACAGATAAAGC	55764
rs769225562	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129448525	CAGTTGGGTTATTTA[C/T]GTGGCCAGCGCCATG	55764
rs769225639	snp	G/T	1.65318e-05	0.002875	synonymous-codon	IFT122	GRCh38.p7	3:129514515	GTCCATTGAGCTGGG[G/T]ACCCTGACCATCCGC	55764
rs769267673	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129495037	TTGGGCAGAAACCCT[A/C]AACATTCTCCTGCTC	55764
rs769283518	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129453517	GTGATTGTGTCTTTT[C/T]CTCCAGCGATTTTGA	55764
rs769283635	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469645	TTTTAGAAATGAGTA[A/G]ACCAGAACTCAGAGC	55764
rs769329698	snp	A/C/T	4.97594e-05	0.00498775	intron-variant	IFT122	GRCh38.p7	3:129514569	GGTGAGGATGCAGCA[A/C/T]CCTTGGGCAGGTGGC	55764
rs769355730	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129508972	AATCATTTCACCAGG[A/T]TCAGACAACTGTAGT	55764
rs769357574	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482286	GTGGCCTGAGGAAGT[A/G]TGTCACCAGAGAAGA	55764
rs769374026	snp	A/G	1.65236e-05	0.00287429	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504473	GGAGAAGTTACTGCC[A/G]AGACATACATTTCAG	55764
rs769375656	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129461093	GAATTAATTTCTGTG[C/T]TTTTTGTTGGTCACT	55764
rs769409756	snp	C/G	1.65132e-05	0.00287339	intron-variant	IFT122	GRCh38.p7	3:129452027	CTGGGTTTCCATTCT[C/G]TATAATAGCCTCATC	55764
rs769442256	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487001	GTTTTGCTCTGAGAG[C/T]AGACAGACTCAAAAT	55764
rs769445554	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483271	TGCTTACTCAAAAAT[C/T]CCAACAACACGCAGG	55764
rs769525127	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440627	TCCCTCACGGTCTGG[C/G]CCTGTCGCTGCCTTG	55764
rs769527595	snp	G/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464754	GCTCCCTCTCGCCAA[G/T]ATGGTCCATCTGCTG	55764
rs769554099	snp	A/G			downstream-variant-500B	IFT122	GRCh38.p7	3:129520675	TGCAACTTAATTTCC[A/G]TATGCAAAAGTGCAC	55764
rs769588653	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129452768	TATTTTAAAAGGATC[C/T]CTCTAGTTGCTGAGT	55764
rs769595673	snp	A/C	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506461	GGTGCTGGAGCAGCT[A/C]ACAAACAATGCCGTG	55764
rs769601983	snp	C/T	3.29658e-05	0.00405978	missense	IFT122	GRCh38.p7	3:129495503	GCAGATGTGTTTTCC[C/T]ACCAGGGGAAGTTCC	55764
rs769612029	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441485	TTTCCTCTATTTTAT[A/G]TATGAGGAAACTGAA	55764
rs769641859	in-del	-/AT	1.64738e-05	0.00286995	frameshift-variant	IFT122	GRCh38.p7	3:129500067	CATGGCTGGGTTGAC[-/AT]GTAGGTTTTGGTCCC	55764
rs769645369	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129510716	CAGGACCTACATGGG[A/T]CTAGGAGCTAAGGGG	55764
rs769712676	snp	C/G	1.64735e-05	0.00286993	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476663	TCTCTCACCCCGCAG[C/G]TGGTCGGCTGCCAGG	55764
rs769736492	snp	A/G	1.64741e-05	0.00286998	intron-variant, missense	IFT122	GRCh38.p7	3:129466892	TTACTGTCTACAGCC[A/G]ATGGGAGAGTTTCTG	55764
rs769736894	in-del	-/CCCACCA	1.64819e-05	0.00287066	intron-variant	IFT122	GRCh38.p7	3:129512439	TTATCCCTCCTCCGT[-/CCCACCA]CCCACCACCGTTCTT	55764
rs769765382	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474505	GAGAAGTGCAATGGG[A/C]TAGGCGAGCACAAGT	55764
rs769768700	in-del	-/AGAC			intron-variant	IFT122	GRCh38.p7	3:129469969	GAAAGCTGTACAGAT[-/AGAC]AGCTTTTTGGGACAC	55764
rs769816487	snp	C/T	1.64781e-05	0.00287033	intron-variant	IFT122	GRCh38.p7	3:129512424	AAGTGTATCCTTTCT[C/T]TTATCCCTCCTCCGT	55764
rs769827508	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129468197	CCACTCTTGGCTGGG[-/T]TTTACAAACAAGGCT	55764
rs769827974	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477776	AGTGATGGTAACAGT[A/G]AGTAGTTTATTTCCA	55764
rs769836048	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129505470	ACCCAGTTGCTGAAG[C/T]ATCTGCATGTTTGGG	55764
rs769859137	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476090	GACTAGGGGAGGTGC[C/T]ACTGACTCCAGGAGC	55764
rs769921357	snp	C/T	4.94173e-05	0.00497053	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476490	CGTGTCAAGCGAAAC[C/T]GGATTCCAACTATGT	55764
rs769954941	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129459511	AGCTAGGATGGTCTC[G/T]ATCTCCTGACTACAT	55764
rs769999922	in-del	-/GT	4.94185e-05	0.00497059	intron-variant	IFT122	GRCh38.p7	3:129449954	TAGGATTTTGTCTTA[-/GT]TTCCTCTTAAAGTGC	55764
rs770004383	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129485178	CCTTGCACCTGTCCC[-/A]ACTTGGCGCCTTGGC	55764
rs770005620	snp	C/T	1.93842e-05	0.00311315	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520261	AGGATGACCCTGGCC[C/T]ATGACCAGCATCCTG	55764
rs770005650	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129464320	AGGGGATTGAGATGG[A/G]GAGTGGGAAGTGGTG	55764
rs770074417	snp	A/G	4.94214e-05	0.00497074	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504397	TGGCTAGCAGAGAAC[A/G]ATCGCTTTGAGGAAG	55764
rs770099276	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129487200	GGCCACTGAAGCACA[C/T]TGGCTGGCCTAAAAC	55764
rs770119900	snp	C/T	9.56069e-05	0.00691334	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440314	TAGGAGGAGCCCGAG[C/T]CGTAAGGGAAGCCGT	55764
rs770122719	snp	A/G	1.64749e-05	0.00287005	missense	IFT122	GRCh38.p7	3:129479887	GGTGGCCCTCCTGGA[A/G]GAGAAGGCCTCTTAG	55764
rs770135337	snp	A/C	1.64765e-05	0.00287019	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507697	GACACAATGCTTGGC[A/C]AGTTCTACCACTTCC	55764
rs770159056	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129518517	TGCTGAAGGAAAGAC[A/G]GACCCATCTCTGCCA	55764
rs770182811	snp	C/T	1.64787e-05	0.00287038	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507619	GGGCCAGTTGGCAGC[C/T]ACAGACACTGTTTGA	55764
rs770194578	snp	A/T			intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129456225	CTTTTCATCACCATC[A/T]CCTGCTACCTACCAG	55764
rs770209993	snp	A/G	1.65091e-05	0.00287303	intron-variant	IFT122	GRCh38.p7	3:129463546	ATCTTCTTTTATATT[A/G]TTGTGCATTGAAGGG	55764
rs770219282	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490438	AGGTTCCTCCCTATT[C/T]CCAGGCTTCCCTCTG	55764
rs770227964	snp	C/G	0.000498058	0.0157728	intron-variant	IFT122	GRCh38.p7	3:129488419	ATCTAGCCAGCAGGA[C/G]CTGGAGTTTGGTCCT	55764
rs770247484	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129503280	GCTGGGTAGCATTTT[A/G]GCAGAAAGCACCATC	55764
rs770258262	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129512235	TGTCACTCAGAATTA[C/T]TGGTGTCTGCCTTTT	55764
rs770353342	snp	A/G	1.83815e-05	0.00303157	intron-variant	IFT122	GRCh38.p7	3:129467105	AACCCTTCTGGTAAG[A/G]GCCCAGGCCCCACAC	55764
rs770359205	snp	A/C	1.6483e-05	0.00287076	splice-acceptor-variant	IFT122	GRCh38.p7	3:129499900	TTGTTGTGCTTCCTC[A/C]GGATTTCCTTGGATC	55764
rs770368547	snp	A/G	1.65263e-05	0.00287452	intron-variant	IFT122	GRCh38.p7	3:129460805	CGCCTTGCATGGTAC[A/G]TGATTTGCTCAGCTT	55764
rs770396563	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483455	GCCCAGGGTGGTTCT[C/T]ACAGGATCCCCACTG	55764
rs770407778	snp	C/G	1.64746e-05	0.00287002	missense, intron-variant	IFT122	GRCh38.p7	3:129460903	CTTCCATTTCTGGGC[C/G]TCCACAAAACAGTAA	55764
rs770413308	snp	G/T	0.00186666	0.0304934	missense	IFT122	GRCh38.p7	3:129519611	TGGTGAGCCGGCTGG[G/T]GCTGCGCTCCATGAG	55764
rs770420689	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129442947	ACTCCCTAGTTTTCT[A/C]CTTTAAATGCACAGC	55764
rs770441242	snp	G/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469364	CGTAATGACATCCTG[G/T]CTGTGGCTGACTGGG	55764
rs770453499	in-del	-/AA	1.6473e-05	0.00286988	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451962	CCCCTCAAGGGACAC[-/AA]AGACACTGTGTACTG	55764
rs770507091	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129509965	AATATTGGAAGAGTA[C/T]CTAGCACAGAGTGAC	55764
rs770529495	snp	G/T	1.65263e-05	0.00287452	missense	IFT122	GRCh38.p7	3:129514501	GCCAGATTCCAAAAG[G/T]CCATTGAGCTGGGTA	55764
rs770542599	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510816	ATAAATGCCTACTAC[A/G]TGACAGACCCTGTGA	55764
rs770562647	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129442787	TCCCAATTACTTTCC[A/G]TGTCAAGTCGTGCAT	55764
rs770572165	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471587	GGGCCACAGGAAATA[C/T]CTTGCATGTATGCAG	55764
rs770572794	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464748	CGGGGGGCTCCCTCT[C/T]GCCAATATGGTCCAT	55764
rs770584231	snp	C/G	0.000284426	0.0119219	missense	IFT122	GRCh38.p7	3:129514445	GTGCCTACAGGCTGG[C/G]CCGGCACGCCTATGA	55764
rs770590297	snp	A/C	1.6473e-05	0.00286988	stop-gained	IFT122	GRCh38.p7	3:129500006	CGCCGTGGAGATGTA[A/C]ATCTCAGCAGGAGAG	55764
rs770612893	in-del	-/TACTT	1.64803e-05	0.00287052	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476360	CCCTGCTGCATCAGC[-/TACTT]TACTAAAGGCGAGTA	55764
rs770628119	snp	A/G	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129492228	TTCCTTCTCAAGAAG[A/G]CATACTTGGGGTTCC	55764
rs770693352	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129518684	CCCCACCACTGTGGG[A/C]GAGGGGCGGTTTCCA	55764
rs770709240	snp	A/C	1.64882e-05	0.00287121	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504448	AGACTGTCACCTTCT[A/C]GAAGGAGCAGGAGAA	55764
rs770720022	snp	A/G	3.7092e-05	0.00430635	intron-variant	IFT122	GRCh38.p7	3:129481505	GCCATGGTGACTGAC[A/G]CTGTTTTCGCTGAAA	55764
rs770732553	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129519486	CTCTCACCACTGCCA[A/T]AGATTCCAGGATCAT	55764
rs770760201	snp	A/G	1.65592e-05	0.00287738	missense	IFT122	GRCh38.p7	3:129514547	CCAAGCCCTTCCACG[A/G]CAGTGAGGTGAGGAT	55764
rs770762310	snp	A/T	1.64732e-05	0.0028699	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504374	ACATCTACATGCCGT[A/T]TGCTCAGTGGCTAGC	55764
rs770787030	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129444160	AGGTGAGAATGAAAG[C/G]TCAGATAGGAGATCA	55764
rs770821151	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129506198	AGTCGCCTTTTCCCA[G/T]CCAAAAAGGAATTTA	55764
rs770833995	snp	C/G	1.64898e-05	0.00287135	intron-variant	IFT122	GRCh38.p7	3:129452012	TGGTAAAAGGCTGCT[C/G]TGGGTTTCCATTCTC	55764
rs770844874	snp	A/G	1.65034e-05	0.00287253	synonymous-codon	IFT122	GRCh38.p7	3:129495481	GACCAACAATGACCT[A/G]TTTCTGGCAGATGTG	55764
rs770854698	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129460447	TTTTTTTTCTTTATT[-/A]TTATTTTTTTTTATG	55764
rs770863285	snp	C/T	3.29457e-05	0.00405854	missense	IFT122	GRCh38.p7	3:129517561	GTGCTGAGACCCAAG[C/T]GGGATGACAGACAGC	55764
rs770992589	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129448580	TGGTGACAAATTAAA[A/G]GGAGGACAGAACCTC	55764
rs771002411	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129480112	GTGCTGTGGCCCTCA[C/T]ACTCCTAGCAGGCCC	55764
rs771046242	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451492	TTTCAAATTCTTGGT[A/G]GCAAATATGAAACAT	55764
rs771062353	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129510779	CAGCTGAATCTTATT[A/C]ATTGGGCCATTCCTT	55764
rs771090115	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129467099	AGTGGGAACCCTTCT[C/G]GTAAGGGCCCAGGCC	55764
rs771092154	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129512320	ACTGCAGGAAGATCC[A/G]TTCAGTGTCCATCGT	55764
rs771115196	snp	C/T	0.000247286	0.0111167	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476347	ACTGAACTTTGACCC[C/T]TGCTGCATCAGCTAC	55764
rs771134246	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129452368	AGGTGATAACTGTTA[C/T]GGAAGAAGAAAAAGT	55764
rs771174610	snp	C/T	1.64762e-05	0.00287016	intron-variant	IFT122	GRCh38.p7	3:129519066	GCTAGGGTCTGTCTC[C/T]ATCTCTGCTTCTGAT	55764
rs771209610	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129463408	ATAAATGGAATCGTA[C/T]AGTATATGACCTTTT	55764
rs771246783	in-del	-/TTA			intron-variant	IFT122	GRCh38.p7	3:129469582	ATACTTTATCCTATT[-/TTA]TTCTTATAAAACCCA	55764
rs771274268	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129456409	TTTGGGAAGCCAAGG[C/T]GGGTGGATCATGAGG	55764
rs771303473	snp	G/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129507023	ACAAGGAGATGTTCT[G/T]CTCCACTGGACAAGG	55764
rs771310196	snp	A/G	1.65119e-05	0.00287327	intron-variant	IFT122	GRCh38.p7	3:129488212	CTGGTTCTTTCCATG[A/G]CTCTGAAAACAGTCT	55764
rs771324957	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129445322	CAGAGCAAGACTCCA[A/C]CTCAAAAAAAACAAA	55764
rs771328041	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129467145	AGGACAGATGTTAAA[C/T]TCTTTGGCCAAGGGA	55764
rs771330076	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439956	GTCTGAATGTTGCGA[A/G]AGCGCCCCAGACGCC	55764
rs771348236	snp	A/G	1.6473e-05	0.00286988	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476466	GGGAGCAGAACTCCT[A/G]GGTGTGGACGTGTCA	55764
rs771368193	snp	A/G	3.73518e-05	0.0043214	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520248	TGCCGCAGGTGCAAG[A/G]ATGACCCTGGCCCAT	55764
rs771372241	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129444011	CACATACCAAGGATG[A/G]CTTTAGATGAGAGGT	55764
rs771398280	snp	A/G	9.73094e-05	0.00697461	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440300	GACGCTGAGGCGGGT[A/G]GGAGGAGCCCGAGCC	55764
rs771398986	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516695	CACAGATTGCTCCTG[-/CA]CACACACACACACAC	55764
rs771409671	snp	A/G	1.65743e-05	0.00287869	intron-variant	IFT122	GRCh38.p7	3:129515473	GCCCCTCGGGAGTCC[A/G]TGGCTGTTTTGTAGG	55764
rs771419749	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441080	ATGACTTTGTCACCT[C/T]TTGATTCAGTTATTT	55764
rs771422778	snp	C/T	3.29571e-05	0.00405924	synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458624	TGCTTCTGGATCAGC[C/T]GACAAAAGCGTTATT	55764
rs771427655	snp	A/G	4.94222e-05	0.00497078	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479828	GCGGAGTGAAGGAGC[A/G]GGAGTGGCAGATGGA	55764
rs771443571	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485797	GTCTTGCTGACTGCA[C/T]CAAGGCCATCCTGCT	55764
rs771445125	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129513466	TCAAATCAAGGGGTG[C/G]CTTCCTGGAGTCAGA	55764
rs771487495	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129491982	ATGCCTCGCTGGGTG[A/G]TATAACCTCCTGCAC	55764
rs771488065	snp	G/T	4.9423e-05	0.00497082	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479799	GGAGAAACGGCTGCA[G/T]TGCCTGTCCTTCAGC	55764
rs771497680	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506482	CAATGCCGTGGCGGA[A/G]AGCAGGTTTAATGAT	55764
rs771499492	snp	C/T	5.76585e-05	0.00536898	missense	IFT122	GRCh38.p7	3:129515566	GTCTGCATCAACTGC[C/T]GCCAGCCCTTCATCT	55764
rs771512628	in-del	-/GCACTGA	1.64773e-05	0.00287026	intron-variant	IFT122	GRCh38.p7	3:129476550	CCATGGCTTGAAGAG[-/GCACTGA]GCAGCCGCCGTGTCT	55764
rs771535468	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129473074	TGGAGGCCAAGGAGG[G/T]ACGATTGCTTGAGGC	55764
rs771564366	snp	A/C	1.77685e-05	0.00298059	intron-variant	IFT122	GRCh38.p7	3:129467092	CCCAGTGAGTGGGAA[A/C]CCTTCTGGTAAGGGC	55764
rs771577138	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493588	ATTCAAGCCCAGTCT[A/G]TTTCCTAAGCTCATG	55764
rs771592180	in-del	-/CTT	6.58903e-05	0.00573941	cds-indel	IFT122	GRCh38.p7	3:129488315	AAGCCTACCAGATTG[-/CTT]GCTTGGGTGTCACAG	55764
rs771622626	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456631	GACAGAGCTAGACTC[C/T]GTCTCAAAAAGGGCC	55764
rs771640929	snp	G/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438832	CCAGCTACTAAGGAG[G/T]CCGGGGTAGGAGGAC	55764
rs771699714	snp	A/T	1.64803e-05	0.00287052	intron-variant	IFT122	GRCh38.p7	3:129483477	TCCCCACTGTCCCTG[A/T]TCCCCAGGAACCAAA	55764
rs771715498	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129462980	GCAGTGTCAAAGTTA[C/T]AAACAATGAAACTGT	55764
rs771730429	snp	G/T	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129506579	GCCAGACCACTGTTT[G/T]CCCAAGCCCCACTCT	55764
rs771758121	snp	A/G	3.30929e-05	0.0040676	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504271	ACAGTGTTTTCATGG[A/G]GGCTGCAGGGGCAGC	55764
rs771797653	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473537	TTTGCTGGGCTCAAA[A/G]TCAAAACTCCATGTT	55764
rs771805158	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129449983	TGCTTCCCTAACCTC[C/T]CTCTTGTGAGTACTC	55764
rs771871899	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492055	GGCTCACTGTCTAGA[C/T]AGAGCTTGACTTCCC	55764
rs771877526	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129508566	TGAATTTTAAATCAT[C/T]ATAACTAGGCTCAAA	55764
rs771889364	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129446793	TTCAGATATTTTACA[C/G]AGTTTGATTTTTTGT	55764
rs771890344	snp	A/G	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476724	TCAGCACAGTCCATG[A/G]GCTTTACAAGGACCG	55764
rs771897587	snp	C/T	3.30453e-05	0.00406467	missense	IFT122	GRCh38.p7	3:129514483	CGTGGCCTGTACATC[C/T]CTGCCAGATTCCAAA	55764
rs771936312	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129481934	TTGCCAATGGAAACC[-/G]AAGGCTCTGAGCCAG	55764
rs771999581	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129452557	GAAGAGAGCTCTTTG[C/T]AGAGGAAGAGCCATT	55764
rs772034346	snp	C/G	1.64746e-05	0.00287002	missense	IFT122	GRCh38.p7	3:129517523	TCACTGATGAAGAAG[C/G]CATCTCCCTCATCGA	55764
rs772034466	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451297	TTTTTATTTATTTTT[A/G]TTTTTTGTAGAGATG	55764
rs772061493	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129484802	CAAAATTTAGGGTAA[C/T]TGTAGACTCACATAA	55764
rs772070215	snp	A/G	1.64765e-05	0.00287019	intron-variant	IFT122	GRCh38.p7	3:129451876	AATTCTGACTAATAG[A/G]TATCACATAGATAAT	55764
rs772087845	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129515934	CCCAGCTCCTTTGAT[A/G]TTGACAGAGGATCAG	55764
rs772158524	snp	C/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464739	TCGAGCGGCCGGGGG[C/G]CTCCCTCTCGCCAAT	55764
rs772212316	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449909	CTGATGGAACTCAAC[C/T]GATTTTGGCTGCCGG	55764
rs772213560	snp	C/T	3.29451e-05	0.00405851	intron-variant	IFT122	GRCh38.p7	3:129512307	TTGCTTTTCTCTCAC[C/T]GCAGGAAGATCCGTT	55764
rs772233400	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468407	GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC	55764
rs772236956	snp	C/T	9.93131e-05	0.00704604	intron-variant	IFT122	GRCh38.p7	3:129517448	CTCCAGCCCCCTCAG[C/T]CCTTTCTCTATGCCC	55764
rs772246533	snp	G/T	1.6476e-05	0.00287014	intron-variant	IFT122	GRCh38.p7	3:129469431	AGGTATGTAGCCCTG[G/T]ACAAATCCAATTGCA	55764
rs772251048	in-del	-/C	1.6588e-05	0.00287988	intron-variant	IFT122	GRCh38.p7	3:129514569	GGTGAGGATGCAGCA[-/C]CCTTGGGCAGGTGGC	55764
rs772253814	snp	C/G	1.83967e-05	0.00303282	intron-variant	IFT122	GRCh38.p7	3:129481490	GGCCAGGATCTTGTT[C/G]CCATGGTGACTGACA	55764
rs772322867	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441860	ATAAACGTACCTATA[A/G]CACAAGCTGATGATA	55764
rs772348994	snp	A/G	1.65457e-05	0.00287621	missense, intron-variant	IFT122	GRCh38.p7	3:129460945	ACAGATAAAGCACCT[A/G]AAGGCCAAGGTGGGA	55764
rs772351452	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474864	ATATATAAAGAGCTA[G/T]AAAGACAGGGCTGGG	55764
rs772362721	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129445641	CAGCATAGCGCGTTA[A/G]TTACAAGCACAGACT	55764
rs772371247	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129480284	CTCCTGATTAGGGCA[-/G]GCGAGTGGATTAAGG	55764
rs772440008	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482432	CCCAAAGCTGGAGCC[C/T]CTCCTGACTGGTTTC	55764
rs772447875	snp	C/G/T	4.94216e-05	0.00497079	synonymous-codon	IFT122	GRCh38.p7	3:129512395	GCCCAAGGACACCCC[C/G/T]TCGGGCATCTCTAAA	55764
rs772449112	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129443561	TCCAATTCTGAGTTT[C/G]TGGTGATTTCATAAT	55764
rs772456145	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129446784	ATAAATCTCTTCAGA[G/T]ATTTTACAGAGTTTG	55764
rs772464740	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129467286	CTGAAAAGACTAAAG[A/G]AGAAAGTTCAACTTT	55764
rs772500842	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503840	ACCATGGCTCATGTC[C/T]GGTTCTCCTGGCCTG	55764
rs772509546	snp	A/T	1.66327e-05	0.00288376	intron-variant	IFT122	GRCh38.p7	3:129488198	GGCTCTGTATGCATC[A/T]GGTTCTTTCCATGGC	55764
rs772535030	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129467085	AGTGTGTCCCAGTGA[A/G]TGGGAACCCTTCTGG	55764
rs772574118	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129469786	CCTCTATTCGCTTTC[-/T]TTCATTCAACCAGTA	55764
rs772633848	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509826	TTAGTGGGTAAACTC[A/G]AGAGTCCTCACACAC	55764
rs772643717	snp	A/C	4.96586e-05	0.00498265	intron-variant	IFT122	GRCh38.p7	3:129519229	AGGAGGGCAGCCTCC[A/C]TCCCTTCTCCTGTGC	55764
rs772671195	snp	A/C	4.97616e-05	0.00498782	intron-variant	IFT122	GRCh38.p7	3:129514571	TGAGGATGCAGCACC[A/C]TTGGGCAGGTGGCTT	55764
rs772671401	snp	A/G	1.82364e-05	0.00301958	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520234	GCTGCTGCCCCTACT[A/G]CCGCAGGTGCAAGGA	55764
rs772695284	snp	C/T	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476729	ACAGTCCATGGGCTT[C/T]ACAAGGACCGCTATG	55764
rs772711174	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129482323	GGCAGCTCTGTGCCC[C/T]GGGCCTGGTTGGCTT	55764
rs772718756	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129479694	GAATGTGTAGGTATT[G/T]TCTCCCCTTAGGGAC	55764
rs772722363	snp	C/T	2.18539e-05	0.00330552	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520137	TAGGGCTGATGAGCA[C/T]TAGGGCTTCAGCCTG	55764
rs772730019	in-del	-/A			downstream-variant-500B	IFT122	GRCh38.p7	3:129520715	TTTGAAAGGAACATT[-/A]ACATTTGTGTGCTCT	55764
rs772799159	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483281	AAAATTCCAACAACA[C/T]GCAGGTGCATGGAGG	55764
rs772835552	snp	C/T			synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458633	ATCAGCTGACAAAAG[C/T]GTTATTATCTGGACA	55764
rs772842069	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129489419	AAAGGGGAATTTAAA[G/T]CAGGGATGGTTGTGC	55764
rs772870247	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129468687	AGCTTGCTCTCCAGC[C/T]TCAGGCAAGGGAGTT	55764
rs772903693	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129508990	AGACAACTGTAGTGG[A/G]TCAGACCAGCAGCAG	55764
rs772926277	in-del	-/TG	0.00014832	0.00861035	intron-variant	IFT122	GRCh38.p7	3:129449988	CCCTAACCTCCCTCT[-/TG]TGAGTACTCTGAAAT	55764
rs772965904	snp	G/T	1.64741e-05	0.00286998	intron-variant	IFT122	GRCh38.p7	3:129449833	CAGACTTCATCATTT[G/T]GGTTCCTAATTGTCT	55764
rs772967589	snp	G/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464662	TGGTCAGTACCTGGC[G/T]CTGGGGATGTTCAAT	55764
rs773010467	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129468323	AGGTGGATTAAGACC[C/T]AGCCTCAAGGGCTAG	55764
rs773053690	snp	C/T	0.000133065	0.00815566	intron-variant	IFT122	GRCh38.p7	3:129463643	TAAGTGCAGCTCTGA[C/T]GATAAGATTTATGTT	55764
rs773056789	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129447080	GCAACATCTTGCACA[C/T]AGCCAGATGTTTCAG	55764
rs773060380	in-del	-/G			intron-variant	IFT122	GRCh38.p7	3:129486647	AACAAAGGGAAAGGT[-/G]GGGGTAGGAACAAGA	55764
rs773078491	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129518557	CCTCAGGTGCCACAG[A/T]TGATATGTGCTATGG	55764
rs773080594	snp	C/T	0.000131783	0.00811628	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504400	CTAGCAGAGAACGAT[C/T]GCTTTGAGGAAGCCC	55764
rs773090330	snp	G/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449915	GAACTCAACTGATTT[G/T]GGCTGCCGGAAGCAG	55764
rs773099831	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129513748	CTGCACTGCAGACGG[C/T]GGGAGCAGGAACACT	55764
rs773100565	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129470093	TTGGGAATGGTGTTT[C/G]AGGCAGAAAAAAAAA	55764
rs773102091	snp	A/G	3.30994e-05	0.004068	intron-variant	IFT122	GRCh38.p7	3:129476826	AGGTCCAGACCTTGG[A/G]AAGAGGGACAGGTGG	55764
rs773116649	snp	A/G	1.65416e-05	0.00287586	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504272	CAGTGTTTTCATGGG[A/G]GCTGCAGGGGCAGCT	55764
rs773157004	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129478631	TTATTTTTAGTAGAG[A/C]CGCGAGGCTGTACTT	55764
rs773170442	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129517825	GCACCTTGGTCTTCC[C/T]GTGTGGGTCTCCCAC	55764
rs773193155	in-del	-/G	1.64876e-05	0.00287116	intron-variant	IFT122	GRCh38.p7	3:129512461	CCGTTCTTGTCTAAT[-/G]GGCCCCAAGAAATTC	55764
rs773204392	snp	C/T	1.64746e-05	0.00287002	intron-variant	IFT122	GRCh38.p7	3:129492108	TTGAAGCCAAGAAGA[C/T]AGCTTATTTTATTCT	55764
rs773215307	snp	C/T	4.94393e-05	0.00497164	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507715	TTCTACCACTTCCAG[C/T]GTTTGGCAGAGCTGT	55764
rs773223574	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129459245	ATCAGTATTGCTCAT[C/G]GGCCTGTAAGTTCCA	55764
rs773232116	snp	A/G	1.64762e-05	0.00287016	intron-variant	IFT122	GRCh38.p7	3:129479929	AATGGACAGGTGAGT[A/G]CTCCCTCACGTCTCC	55764
rs773269692	snp	A/G	1.6473e-05	0.00286988	missense	IFT122	GRCh38.p7	3:129500034	GAGCACGTCAAGGCC[A/G]TCGAGATCTGTGGTG	55764
rs773272972	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511237	TCCCTACCTAGTGCA[A/G]TAGAACCACAGGCAG	55764
rs773274390	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129463301	TTACCACTTAGTGTC[A/T]TATCTACTCACCTTA	55764
rs773287083	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	IFT122	GRCh38.p7	3:129517539	CATCTCCCTCATCGA[C/T]CTGGAGGTGCTGAGA	55764
rs773311961	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129461142	CTAAAGTCAGAGGCT[A/G]TGGGCTCATTATTAA	55764
rs773356978	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129485180	TTGCACCTGTCCCAA[C/T]TTGGCGCCTTGGCAT	55764
rs773364715	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129450278	AAGCAACAGGACTGA[C/T]GGTGCTGTGTCCATG	55764
rs773364811	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129464372	CAAGCTAAGGGCTGT[C/T]ATAGAGGTATGTACA	55764
rs773378008	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129467988	ACTGATCCATCTCAC[-/AG]GGACTGAGCCCAGCC	55764
rs773399824	snp	A/G/T	3.29561e-05	0.00405921	intron-variant	IFT122	GRCh38.p7	3:129500108	AAGCATTTGGCAGCA[A/G/T]GTCATCACATGTCAC	55764
rs773413328	snp	C/G	1.66015e-05	0.00288105	missense, intron-variant	IFT122	GRCh38.p7	3:129460948	GATAAAGCACCTAAA[C/G]GCCAAGGTGGGAGGA	55764
rs773414862	snp	A/G	1.69856e-05	0.00291419	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439704	CAGGTGGTGAAACTG[A/G]GGCCCAAAAGGGGAC	55764
rs773433523	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129455215	TCTCGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	55764
rs773452716	snp	C/T	1.64727e-05	0.00286986	intron-variant	IFT122	GRCh38.p7	3:129512309	GCTTTTCTCTCACTG[C/T]AGGAAGATCCGTTCA	55764
rs773457779	snp	A/C/T	1.66729e-05	0.00288724	intron-variant	IFT122	GRCh38.p7	3:129488195	GCAGGCTCTGTATGC[A/C/T]TCTGGTTCTTTCCAT	55764
rs773496085	snp	G/T	3.70158e-05	0.00430192	intron-variant	IFT122	GRCh38.p7	3:129481498	TCTTGTTGCCATGGT[G/T]ACTGACACTGTTTTC	55764
rs773504820	snp	C/T	1.65206e-05	0.00287403	intron-variant	IFT122	GRCh38.p7	3:129461195	AATCTTTGTGGTTTG[C/T]TGCATAGTAATCTAC	55764
rs773512823	snp	G/T	9.66464e-05	0.00695082	intron-variant	IFT122	GRCh38.p7	3:129483693	CGCAGGTAACTGGGG[G/T]TGCCTGTCCACTCTT	55764
rs773531126	snp	A/G	1.6507e-05	0.00287284	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476330	ATTGGAAAGGATCGG[A/G]CACTGAACTTTGACC	55764
rs773557692	snp	C/T	1.65255e-05	0.00287445	missense	IFT122	GRCh38.p7	3:129519719	CCATTACCATGTGCC[C/T]CTCCTGCTTCCAGGT	55764
rs773559408	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505544	AGAATCCATCACCAT[A/G]GTAACTTGGTACTCA	55764
rs773603056	snp	A/G	1.64901e-05	0.00287137	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478103	AGAAAATCCTCATCT[A/G]TGAGTTGTATTCAGA	55764
rs773620629	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129485040	ACCTGCCTTGTATTT[A/G]CAGCTGCATTTTATT	55764
rs773635955	in-del	-/CTTT			intron-variant	IFT122	GRCh38.p7	3:129459773	TTCCTTCCTTCCTTC[-/CTTT]CTTTTCAGTCTTGCT	55764
rs773649300	snp	C/T	2.16331e-05	0.00328878	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520143	TGATGAGCACTAGGG[C/T]TTCAGCCTGGTCTTA	55764
rs773718674	snp	A/G	4.98211e-05	0.0049908	intron-variant	IFT122	GRCh38.p7	3:129488200	CTCTGTATGCATCTG[A/G]TTCTTTCCATGGCTC	55764
rs773724271	snp	C/T	1.78163e-05	0.0029846	intron-variant	IFT122	GRCh38.p7	3:129478256	AGTTGGGCTGAATTC[C/T]ATTTGTGCTCCCCCC	55764
rs773725932	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129490538	GAACTCGGAAACAGA[C/T]TTATTAATGGGCAAA	55764
rs773736175	snp	A/C/G	3.29501e-05	0.00405884	intron-variant	IFT122	GRCh38.p7	3:129506405	CCCTCCACCACTCCT[A/C/G]CAGCGTTCCACAAGG	55764
rs773792276	snp	C/T	1.64784e-05	0.00287035	intron-variant	IFT122	GRCh38.p7	3:129464786	AACCCTTCAAGGTAC[C/T]CTTAAAGTTGTCCTC	55764
rs773815926	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129477884	TATGTATTAGATACT[C/T]TAAAGATTTTTCAAT	55764
rs773825436	snp	C/G	3.56627e-05	0.00422257	intron-variant	IFT122	GRCh38.p7	3:129515465	CTGCCCCGGCCCCTC[C/G]GGAGTCCGTGGCTGT	55764
rs773854995	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129453120	AAGTTGATGATGTCG[C/G]AGAGGGGAGAGAACT	55764
rs773880661	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129443694	CAAGGCAAGATAATA[C/T]CTAACACAATGTAAA	55764
rs773902277	in-del	-/GTTATTATCT	1.64795e-05	0.00287045	frameshift-variant, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458634	TCAGCTGACAAAAGC[-/GTTATTATCT]GGACATCAAAACTGG	55764
rs773906116	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484482	AGCATGTGGTTTTAT[A/G]AGAACATTTTTAAAC	55764
rs773941074	snp	A/G	1.65119e-05	0.00287327	missense	IFT122	GRCh38.p7	3:129481693	AGGAGCTGCTTTTTC[A/G]GGTGAAGTCCCTGAG	55764
rs773962301	in-del	-/TTTA			downstream-variant-500B	IFT122	GRCh38.p7	3:129520788	CAGGGGGTTTTTTTG[-/TTTA]TTTATTTTGATTTAA	55764
rs773965472	snp	G/T	1.64754e-05	0.00287009	missense	IFT122	GRCh38.p7	3:129495523	GGGGAAGTTCCATGA[G/T]GCCGCCAAACTGTAC	55764
rs773998141	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129511110	CCAGCAGAGCAGCAC[C/T]GATTCAGGGCAAGAC	55764
rs774032010	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129499745	TTCCCGAGACCTGGG[-/A]ACTCCCCCAACTCAG	55764
rs774066146	snp	G/T	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466911	GGAGAGTTTCTGGAT[G/T]AACAGAGAGAATGAG	55764
rs774104621	snp	C/T	1.64795e-05	0.00287045	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458613	GGCAAGCGCTTTGCT[C/T]CTGGATCAGCTGACA	55764
rs774115789	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129497566	GCCCCTGCTCTGAGG[A/C]CCCTCCTTACACTGT	55764
rs774120123	snp	A/G	4.97715e-05	0.00498831	intron-variant	IFT122	GRCh38.p7	3:129463635	GCTGCAGGTAAGTGC[A/G]GCTCTGACGATAAGA	55764
rs774141974	snp	C/T	1.89536e-05	0.00307838	intron-variant	IFT122	GRCh38.p7	3:129514365	TGGTGTTGCCCCTGC[C/T]GTCCTTAACCCTGTT	55764
rs774161565	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129444240	CTCAAAATGTGAAAT[A/G]TGCCAAGGCTCAGAG	55764
rs774176849	snp	C/T	1.64914e-05	0.00287149	intron-variant	IFT122	GRCh38.p7	3:129461332	TCCTGATGTCCTGTC[C/T]TGGAATAACTGAAAA	55764
rs774202017	snp	A/C/G	3.29697e-05	0.00406005	intron-variant	IFT122	GRCh38.p7	3:129483465	GTTCTCACAGGATCC[A/C/G]CACTGTCCCTGTTCC	55764
rs774202691	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129490655	TGGAGCCCAGAAGCA[C/G]AGAAGTAGGCTCAGA	55764
rs774223299	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129518117	GCACTGTCCTCTGGG[C/T]AACTTCATTCTTTGG	55764
rs774228594	snp	C/T	1.67469e-05	0.00289364	intron-variant	IFT122	GRCh38.p7	3:129488445	GTCCTTGTGGGGTCC[C/T]TTAAGAAGGCAGATG	55764
rs774279326	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129467193	AACTGTGGGTGAAAG[C/T]GCCTTCAAAAAAAGG	55764
rs774305891	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129501275	GAGGGTGGCTCAGGC[A/T]GGGTCCTAAAGGCTG	55764
rs774321752	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129506241	TTTTCCAGGATGTAG[C/T]CTTGGTTATTTAGAG	55764
rs774334400	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129465637	ACCACGCCTGGCTAA[-/T]TTTTTTTTTTTTTTT	55764
rs774343448	snp	A/G	1.88294e-05	0.00306828	missense	IFT122	GRCh38.p7	3:129515597	TCTCCGCCTCTTCCT[A/G]CGGTGAGTCCCTGCA	55764
rs774359244	snp	A/T	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479833	GTGAAGGAGCGGGAG[A/T]GGCAGATGGAGTCTC	55764
rs774391989	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129486096	AGATAAAGTATAGCT[C/T]AGAGAGTATTTGTTC	55764
rs774392002	snp	A/G	1.64841e-05	0.00287085	intron-variant	IFT122	GRCh38.p7	3:129479972	AATCTGCATGCACAC[A/G]TGGGTGACCCGTCTA	55764
rs774398524	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129451566	ATGTTGTAGCTGGCT[C/G]TTTTTATGGGCTAGT	55764
rs774399900	in-del	-/CACA			intron-variant	IFT122	GRCh38.p7	3:129516564	CACAGATTGCTCCTG[-/CACA]CACACACACACAGAG	55764
rs774441368	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129512514	GAACCTTCCTCTCTC[A/G]GCAACCCTCAGGGAA	55764
rs774456161	snp	A/G	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449899	GCATTTAAGCCTGAT[A/G]GAACTCAACTGATTT	55764
rs774481659	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129465465	ACTAATTATATGCTC[-/T]TTTTTTTTTTTTTTT	55764
rs774497543	in-del	-/TATAAT			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458163	TACTTCATAAGTAGA[-/TATAAT]TATTATTTGTCAAAA	55764
rs774507004	in-del	-/ACAG			intron-variant	IFT122	GRCh38.p7	3:129517300	CACACACACACACAC[-/ACAG]AGACTGCTCCTGCAC	55764
rs774520824	snp	C/T	3.29565e-05	0.00405921	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507709	GGCAAGTTCTACCAC[C/T]TCCAGCGTTTGGCAG	55764
rs774552629	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129444067	ATCCACCATAGCAAT[A/C]CACAAGTGTCAGGCG	55764
rs774582025	snp	A/C			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440660	TTCATCTCACACCCA[A/C]GAGACAGCACGAAGC	55764
rs774582089	snp	C/T	1.65985e-05	0.00288079	intron-variant	IFT122	GRCh38.p7	3:129517432	AAGTCCTTTGCAAGG[C/T]CTCCAGCCCCCTCAG	55764
rs774582237	snp	C/T	4.94287e-05	0.00497111	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507644	GTTTGACACGTTTCC[C/T]CTCCCACCCGCTGCA	55764
rs774590709	snp	A/G	3.29527e-05	0.00405898	intron-variant	IFT122	GRCh38.p7	3:129469307	CATCAGCAGGCTGTG[A/G]CCCTTCATAACCTCT	55764
rs774633968	snp	C/T	9.88354e-05	0.00702908	synonymous-codon	IFT122	GRCh38.p7	3:129500024	CTCAGCAGGAGAGCA[C/T]GTCAAGGCCATCGAG	55764
rs774669835	snp	A/G	1.65064e-05	0.00287279	missense, intron-variant	IFT122	GRCh38.p7	3:129460936	GTAACAGCCACAGAT[A/G]AAGCACCTAAAGGCC	55764
rs774682579	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487045	TCAATTCTAAAGCTA[A/G]AAAATGGGACTGGAA	55764
rs774686011	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439964	GTTGCGAAAGCGCCC[C/T]AGACGCCGCCGCTGC	55764
rs774687371	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129451761	CCCAACTTTAAGTCA[C/T]GTTGTTTTTGGTTTT	55764
rs774723842	snp	C/T	6.75813e-05	0.00581258	missense	IFT122	GRCh38.p7	3:129483590	ACCTTCCCTGTGCAC[C/T]GGCAGAAGCTGCAGG	55764
rs774749353	in-del	-/GCCCCGAGAA	1.64741e-05	0.00286998	intron-variant	IFT122	GRCh38.p7	3:129500085	TAGGTTTTGGTCCCT[-/GCCCCGAGAA]GCATTTGGCAGCATG	55764
rs774797598	snp	A/G			splice-acceptor-variant	IFT122	GRCh38.p7	3:129506408	TCCACCACTCCTACA[A/G]CGTTCCACAAGGCTG	55764
rs774808780	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482177	CAAGCCTGGCCTTCT[A/G]CTTAATTCACAAGAA	55764
rs774821607	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129502676	CGTTGACAAGACCCA[A/G]AGCCCACCCTCCTAC	55764
rs774859282	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129492012	CGCACGATGATTAAT[C/T]TGTGCTTGCTCCCTT	55764
rs774872663	snp	A/G	7.91546e-05	0.00629055	synonymous-codon	IFT122	GRCh38.p7	3:129483679	TGCCGTGGAGGTGCC[A/G]CAGGTAACTGGGGGT	55764
rs774913842	snp	C/T	6.61583e-05	0.00575107	synonymous-codon	IFT122	GRCh38.p7	3:129514524	GCTGGGTACCCTGAC[C/T]ATCCGCGCCAAGCCC	55764
rs774915380	snp	C/T			synonymous-codon	IFT122	GRCh38.p7	3:129519705	GCTGCCTGACGCCTC[C/T]ATTACCATGTGCCCC	55764
rs774922049	snp	C/T	1.64754e-05	0.00287009	intron-variant	IFT122	GRCh38.p7	3:129500099	TGCCCCGAGAAGCAT[C/T]TGGCAGCATGTCATC	55764
rs774949584	snp	A/G	3.37667e-05	0.00410879	intron-variant	IFT122	GRCh38.p7	3:129477971	TCTGCCTTGCACCTT[A/G]CATAACAACCTCTTG	55764
rs774970471	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456638	CTAGACTCCGTCTCA[A/G]AAAGGGCCAGTCGTG	55764
rs774992130	snp	C/G	1.65767e-05	0.00287891	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129519783	CTTGGCCACTTTTCC[C/G]TTGCCCAAATGTCCC	55764
rs775040762	snp	A/G	3.29669e-05	0.00405984	intron-variant	IFT122	GRCh38.p7	3:129506370	TGTGTGACTTCCTAA[A/G]TAGCATGTGCTTTTT	55764
rs775052603	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129473089	GACGATTGCTTGAGG[A/C]CAGGAGTTCAAGACT	55764
rs775054195	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129444350	TTTGCCCAGCTGGAA[A/G]GAGTGTGATAATCAT	55764
rs775055121	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129493942	GAAAAAAAGTAAAGT[A/G]CCTTTGAGTGTGCTC	55764
rs775058309	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457144	ACCAGAGTAGGTGAA[G/T]ACCCCGTTATTTGCT	55764
rs775090147	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129446955	GACAGGTTTTTGACA[A/C]ATTCTTACTATAGTC	55764
rs775100550	in-del	-/TG			intron-variant	IFT122	GRCh38.p7	3:129494764	GATACAAGGAATATC[-/TG]GAGTCAGACAGAACT	55764
rs775105041	snp	C/T	1.64808e-05	0.00287057	stop-gained	IFT122	GRCh38.p7	3:129495506	GATGTGTTTTCCTAC[C/T]AGGGGAAGTTCCATG	55764
rs775110253	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511343	GAAATTTACGTGTGA[A/G]CTAAATAGAAAATGC	55764
rs775116041	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470801	TCTCAAGCTCCTGAC[C/T]TCAGGTGATCCACCT	55764
rs775119084	snp	C/T	1.64738e-05	0.00286995	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464765	CCAATATGGTCCATC[C/T]GCTGGAACCCTTCAA	55764
rs775178365	snp	A/G	1.65007e-05	0.00287229	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478080	TCGATTGGCTATCCA[A/G]CTGCCAGAGAAAATC	55764
rs775216505	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129451313	TTTTTTGTAGAGATG[G/T]GGTTTCACTTAGTTG	55764
rs775243045	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129484862	AACCCTTTGCCTAGT[C/T]TCCCCCAACGGTAAC	55764
rs775245806	snp	A/G	1.64741e-05	0.00286998	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466893	TACTGTCTACAGCCG[A/G]TGGGAGAGTTTCTGG	55764
rs775251218	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476491	GTGTCAAGCGAAACC[A/G]GATTCCAACTATGTG	55764
rs775266843	snp	A/G	1.6473e-05	0.00286988	missense	IFT122	GRCh38.p7	3:129517594	GAGATTGCAAACAAC[A/G]GTATCCATGCCCTTG	55764
rs775275550	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516287	CACAGATTGCTCCTG[-/CA]CACACACACACACAC	55764
rs775328391	snp	A/G	1.64741e-05	0.00286998	missense	IFT122	GRCh38.p7	3:129495578	GCGCTTGAAATGTAC[A/G]CCGACCTCTGCATGT	55764
rs775333744	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471961	TGAGGTAAATACTGT[C/T]ATCATCACCATTTTA	55764
rs775361917	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483822	GGGAGGCAGTCTGGG[C/T]CTGGAACCTGCCGCC	55764
rs775365592	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129511823	CATGTGGGTTCATGC[-/T]TGGAGAGGGCTAAAT	55764
rs775372209	snp	A/G	1.65105e-05	0.00287315	intron-variant	IFT122	GRCh38.p7	3:129452029	GGGTTTCCATTCTCT[A/G]TAATAGCCTCATCAT	55764
rs775404805	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129513944	GTGTGCAGACAGAGT[G/T]GGGTACACCCAGGGG	55764
rs775418373	snp	A/C	1.65241e-05	0.00287433	missense	IFT122	GRCh38.p7	3:129481678	ATGACATCGACACCA[A/C]GGAGCTGCTTTTTCA	55764
rs775472680	snp	A/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503953	AGAAGTGGTGATGAT[A/G]ATAATGTCAATTCTG	55764
rs775490325	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129503004	GTGATGGAAGGAACA[C/T]TGGGCTGGCAGTCAG	55764
rs775491043	snp	C/G	9.89266e-05	0.00703232	intron-variant	IFT122	GRCh38.p7	3:129461326	TCTGATTCCTGATGT[C/G]CTGTCCTGGAATAAC	55764
rs775491091	snp	C/G	4.94466e-05	0.00497201	intron-variant	IFT122	GRCh38.p7	3:129488229	TCTGAAAACAGTCTT[C/G]TTTTTTTCCCTTGAT	55764
rs775497377	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441943	TGCAGAGCTCATGCT[C/T]GGCCTAAAAGGGGCA	55764
rs775510906	snp	A/G	1.64773e-05	0.00287026	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476375	TACTTTACTAAAGGC[A/G]AGTACATTTTGCTGG	55764
rs775523921	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129474880	AAAGACAGGGCTGGG[C/T]ATGGTGGTTCACACG	55764
rs775527601	in-del	-/C	1.64931e-05	0.00287163	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476790	TGCAGCACCTGATCA[-/C]TGAGCAGAAAGGTAA	55764
rs775540708	snp	C/T	4.27963e-05	0.00462562	intron-variant	IFT122	GRCh38.p7	3:129514331	CACTCCAAGGACAGG[C/T]AGTGCCAGCTCCTGG	55764
rs775554474	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129513813	GGGGCAGCCAACATC[A/G]GAGGTGACCTGAGAG	55764
rs775568842	snp	C/T	3.79492e-05	0.00435582	synonymous-codon	IFT122	GRCh38.p7	3:129515586	GCCCTTCATCTTCTC[C/T]GCCTCTTCCTACGGT	55764
rs775581477	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438930	CAGAGCGAGACCTCA[C/T]CTCAAAAAAAAACCC	55764
rs775609341	snp	A/G	1.64887e-05	0.00287125	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129463567	CATTGAAGGGTTGTG[A/G]TCTCCTGAACAGAAG	55764
rs775615278	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440954	GCCTTTAAACCTGAG[A/G]TCTCGTTTCTCTAAA	55764
rs775660853	snp	A/T	1.64784e-05	0.00287035	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507630	CAGCCACAGACACTG[A/T]TTGACACGTTTCCCC	55764
rs775676305	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129480321	GTTCCAGCATGTGTC[C/G]TAAAGAATGCTGGGT	55764
rs775681633	snp	C/T	4.46349e-05	0.00472392	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439844	CCCATCGAGCAGGGT[C/T]CGGCTGCAGCAACGA	55764
rs775693589	snp	C/T	1.64808e-05	0.00287057	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458656	TCTGGACATCAAAAC[C/T]GGAAGGCATTCTGAA	55764
rs775733657	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451717	CTGGTCACATAGTAC[A/G]TAGACCTGGGTCCTC	55764
rs775756736	snp	A/G	1.64749e-05	0.00287005	missense	IFT122	GRCh38.p7	3:129479894	CTCCTGGAAGAGAAG[A/G]CCTCTTAGTGGGGCT	55764
rs775768722	in-del	-/CTC	1.66087e-05	0.00288168	intron-variant	IFT122	GRCh38.p7	3:129514587	TTGGGCAGGTGGCTT[-/CTC]CTCTCCCTTGAGGCC	55764
rs775787009	snp	C/T	3.29468e-05	0.00405861	synonymous-codon	IFT122	GRCh38.p7	3:129488316	AGCCTACCAGATTGC[C/T]TGCTTGGGTGTCACA	55764
rs775819020	snp	C/G	1.86886e-05	0.00305679	intron-variant	IFT122	GRCh38.p7	3:129467109	CTTCTGGTAAGGGCC[C/G]AGGCCCCACACAGAC	55764
rs775823678	snp	A/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476216	TCTCCCTGTCTTCCC[A/G]ACTCCCTCTAAAGTT	55764
rs775856007	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453238	CTGCAGAGGCCAGCA[A/G]ATGGGGACAATGTGG	55764
rs775858659	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129510011	TCCTTACTGCTGCTC[C/T]AGGCAAGGCTTCACG	55764
rs775935913	snp	C/T	1.73884e-05	0.00294854	intron-variant	IFT122	GRCh38.p7	3:129460810	TGCATGGTACATGAT[C/T]TGCTCAGCTTTCATT	55764
rs775936679	snp	G/T	0.00013207	0.00812512	synonymous-codon	IFT122	GRCh38.p7	3:129519690	ATACTTCCGCTCACT[G/T]CTGCCTGACGCCTCC	55764
rs775943809	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129501422	TAATAATTGGTGTGT[A/G]GGCCCCTCACAAAGG	55764
rs775991800	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129445843	TCAGCAGGTGCTGTC[C/T]GGAATAAGAGTTCGA	55764
rs775994438	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129480442	GTATACATGTGTACA[C/T]GTGTGTTCTTTGCTC	55764
rs776052135	snp	C/T	4.95929e-05	0.00497936	missense	IFT122	GRCh38.p7	3:129514447	GCCTACAGGCTGGCC[C/T]GGCACGCCTATGACA	55764
rs776058322	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129508899	GAACCAGTGCCAGCT[A/G]CAGGTGTTGCAGTTT	55764
rs776099605	snp	A/C/G/T	4.94315e-05	0.00497131	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507704	TGCTTGGCAAGTTCT[A/C/G/T]CCACTTCCAGCGTTT	55764
rs776119045	snp	C/T	3.29549e-05	0.00405911	missense	IFT122	GRCh38.p7	3:129483488	CCTGTTCCCCAGGAA[C/T]CAAACGCCAACAGTG	55764
rs776136508	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129500615	TCTTCTCTTAGGAGA[C/T]ACTCTTTCCATGAAG	55764
rs776148104	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129507802	CTGAGGGTACCATCT[C/T]CTGAGCTAGGGGTCC	55764
rs776176217	snp	C/T	1.64798e-05	0.00287047	synonymous-codon	IFT122	GRCh38.p7	3:129499907	GCTTCCTCAGGATTT[C/T]CTTGGATCTGGAGAC	55764
rs776188759	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482258	GCGTTGTTCAGTGGA[A/G]TCATCCAGCCCTGTG	55764
rs776191615	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129458766	GATGTAGGAGAAAAC[C/T]TTTTTCTCTTAAATT	55764
rs776220829	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129494783	GTCAGACAGAACTGC[A/G]TCCAAATTCCAGCTC	55764
rs776243443	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129519975	AGCGTGATGTGCCCT[C/T]GACCTTCACTCAGAA	55764
rs776288214	snp	C/G	3.30218e-05	0.00406323	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504286	GGGCTGCAGGGGCAG[C/G]TTTATTAAGACTTCA	55764
rs776301939	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129480995	GGAGTTTGAGGCTGC[A/G]GTGTGATATGATTAT	55764
rs776305866	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129447236	AGAACATGTGCCCAC[A/G]GTGGTTGGGGTGCAG	55764
rs776307587	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129476834	ACCTTGGGAAGAGGG[A/G]CAGGTGGAAGCAGGT	55764
rs776308050	snp	C/T	3.30278e-05	0.0040636	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478059	GAAGATTGCCATCTA[C/T]AGAAATCGATTGGCT	55764
rs776327835	in-del	-/CAGGTC	3.30273e-05	0.00406356	intron-variant	IFT122	GRCh38.p7	3:129476810	CAGAAAGGTAAGAGG[-/CAGGTC]CAGACCTTGGGAAGA	55764
rs776359392	snp	C/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440518	GACTGCAGGGTCGCC[C/G]TCCCGCCCCTTGGCG	55764
rs776368675	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129518160	GCCCCCATAACACAG[A/G]GATGTCAGGAGCAGT	55764
rs776394716	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129449233	GTTCTGTATTTCATC[C/T]AATCTAATAGGTCAT	55764
rs776428756	snp	G/T	1.64727e-05	0.00286986	missense	IFT122	GRCh38.p7	3:129512326	GGAAGATCCGTTCAG[G/T]GTCCATCGTCCTGAA	55764
rs776441282	snp	A/C	1.64958e-05	0.00287187	missense	IFT122	GRCh38.p7	3:129495489	ATGACCTGTTTCTGG[A/C]AGATGTGTTTTCCTA	55764
rs776461059	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129489274	AAGCCTGGCTGAGAA[C/T]GAGCTGTGTCACATA	55764
rs776463861	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129467579	ACTATCCCTTACCTT[A/C]CCTTGCATTTTCTAG	55764
rs776466629	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439132	AAACTGCAAGAACTA[A/G]AATTAGAATCAAGGT	55764
rs776466910	snp	C/T	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129449921	AACTGATTTTGGCTG[C/T]CGGAAGCAGATTACT	55764
rs776521898	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129447644	AGCCTCCCTAGTAGC[-/T]TGGGATTACAGGCGC	55764
rs776547382	snp	C/T	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129492234	CTCAAGAAGGCATAC[C/T]TGGGGTTCCTGTTTT	55764
rs776564295	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472200	CCCTGTTACCCAGGC[C/T]GGAGTGCAGTGGTAT	55764
rs776566286	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129485979	TTCGAAATTTACATT[C/G]TCTTGTGCAAGAACT	55764
rs776614849	in-del	-/C	1.65378e-05	0.00287552	frameshift-variant	IFT122	GRCh38.p7	3:129495467	AGAAGCGGGGAGAGA[-/C]CCAACAATGACCTGT	55764
rs776639270	snp	A/C/G	3.72095e-05	0.00431319	intron-variant	IFT122	GRCh38.p7	3:129481508	ATGGTGACTGACACT[A/C/G]TTTTCGCTGAAATTT	55764
rs776661081	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129461413	AGAGAGTTAATACTA[C/T]TTCTCTACCTTCAAT	55764
rs776691220	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129490342	CAGCTTGGATATAGT[A/G]GTTCCTAGAGATGGA	55764
rs776704844	snp	C/T	0.000461255	0.0151794	intron-variant	IFT122	GRCh38.p7	3:129519076	GTCTCCATCTCTGCT[C/T]CTGATTCCATCCTTG	55764
rs776715650	snp	C/T	1.64757e-05	0.00287012	missense	IFT122	GRCh38.p7	3:129512412	CGGGCATCTCTAAAG[C/T]GTATCCTTTCTCTTA	55764
rs776716339	snp	C/T	1.89669e-05	0.00307946	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520255	GGTGCAAGGATGACC[C/T]TGGCCCATGACCAGC	55764
rs776809208	snp	C/T			intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507442	CCTCAAACTCCCTGG[C/T]CTTATGCCCTGTCCA	55764
rs776815902	snp	C/T	6.60142e-05	0.0057448	intron-variant	IFT122	GRCh38.p7	3:129488214	GGTTCTTTCCATGGC[C/T]CTGAAAACAGTCTTC	55764
rs776829183	snp	C/T	1.65029e-05	0.00287248	intron-variant	IFT122	GRCh38.p7	3:129461206	TTTGCTGCATAGTAA[C/T]CTACAGTTGTTTACT	55764
rs776831197	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129442909	ACCCGAAGATCCTTC[C/T]CAAATGCTCCCTTAT	55764
rs776871553	snp	A/G	1.67666e-05	0.00289534	intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439714	AACTGAGGCCCAAAA[A/G]GGGACAGTAACTTAC	55764
rs776893048	snp	C/T	4.94352e-05	0.00497143	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476365	CTGCATCAGCTACTT[C/T]ACTAAAGGCGAGTAC	55764
rs776909936	snp	A/C	1.66283e-05	0.00288338	intron-variant	IFT122	GRCh38.p7	3:129514594	GGTGGCTTCTCCTCT[A/C]CCTTGAGGCCATCTC	55764
rs776912060	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129484859	TTAAACCCTTTGCCT[A/C]GTTTCCCCCAACGGT	55764
rs776943027	snp	C/T	1.64882e-05	0.00287121	synonymous-codon	IFT122	GRCh38.p7	3:129502760	GAGCGCGAGCCCCTG[C/T]TGCTGTGCGCTACCT	55764
rs776943039	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129462996	AAACAATGAAACTGT[C/T]ATTTCTTTGAGAGTC	55764
rs776961242	snp	A/T	2.07505e-05	0.003221	intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520154	AGGGCTTCAGCCTGG[A/T]CTTACAGCTGTCTTC	55764
rs776988688	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129497592	ACTGTGGTGGACTTC[A/G]TGTGCCCACAGCCTC	55764
rs777023612	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense	IFT122	GRCh38.p7	3:129466942	GATGCCGAGGATGTC[A/G]TTGTCAACAGATATA	55764
rs777049610	snp	C/T	3.59363e-05	0.00423873	intron-variant	IFT122	GRCh38.p7	3:129478269	TCCATTTGTGCTCCC[C/T]CCCCAGTGATAGGGT	55764
rs777051654	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	IFT122	GRCh38.p7	3:129488289	GTACCTGGATAGGAA[A/G]CTGTTCAAGGAAGCC	55764
rs777108020	in-del	-/CA/CACA			intron-variant	IFT122	GRCh38.p7	3:129517268	CACACATTGCTCCTG[-/CA/CACA]CACACACACACACAC	55764
rs777126874	snp	A/G	1.64768e-05	0.00287021	intron-variant, missense	IFT122	GRCh38.p7	3:129467008	TACAGTAGTCAGGGT[A/G]GTGAGGCAGAGGAGG	55764
rs777145517	in-del	-/C	1.64762e-05	0.00287016	frameshift-variant	IFT122	GRCh38.p7	3:129519142	TGGAGACCAAGGACT[-/C]CCATCGGAGATGAGG	55764
rs777167077	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129511119	CAGCACTGATTCAGG[G/T]CAAGACTGGAAAGGG	55764
rs777172396	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129488026	GAAGGAGGGGAGGAT[A/G]GGCAGAGAGTTTGTG	55764
rs777199171	snp	G/T	1.80883e-05	0.00300729	intron-variant	IFT122	GRCh38.p7	3:129467100	GTGGGAACCCTTCTG[G/T]TAAGGGCCCAGGCCC	55764
rs777208935	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505655	GCTCTCATATGGCAA[A/G]TGTCATGGCTACAAG	55764
rs777211509	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129449648	GGCTTCTGGACAAGA[A/G]GAAATCAGGACAAAG	55764
rs777212040	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453587	GAGGTGGTTTTGCAA[A/G]CACATTTGAAGATGA	55764
rs777246844	snp	C/T	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129506581	CAGACCACTGTTTTC[C/T]CAAGCCCCACTCTGA	55764
rs777253192	snp	A/C	1.64784e-05	0.00287035	intron-variant	IFT122	GRCh38.p7	3:129495611	GAGTATGCCAAGGTA[A/C]CCTACCCTGTCCCAG	55764
rs777282151	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129510719	GACCTACATGGGACT[A/T]GGAGCTAAGGGGCCT	55764
rs777296857	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129509105	GAGCTGGTCATCACG[G/T]TTGTCATGTAAAGTC	55764
rs777308171	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506485	TGCCGTGGCGGAGAG[C/T]AGGTTTAATGATGCT	55764
rs777333238	snp	A/C	1.6473e-05	0.00286988	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469361	GAACGTAATGACATC[A/C]TGGCTGTGGCTGACT	55764
rs777340808	in-del	-/TGT			intron-variant	IFT122	GRCh38.p7	3:129494693	TGTGCTAAGTGTGTG[-/TGT]GTGTGTGTGTGTGTT	55764
rs777353653	in-del	-/CACA			intron-variant	IFT122	GRCh38.p7	3:129516099	CACAGACTGCTCCTG[-/CACA]CACACACACAGACTG	55764
rs777373216	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129463789	CTCGATGGGAAAGAC[-/T]TGTGCCTTTGATCAT	55764
rs777374649	snp	A/G	3.30071e-05	0.00406232	synonymous-codon	IFT122	GRCh38.p7	3:129519675	ACCCCTGAGGTGGCA[A/G]TACTTCCGCTCACTG	55764
rs777392475	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129462397	ATTTGAGCTTTATGA[C/T]AGCCCCTGAGGTGTC	55764
rs777402142	snp	A/C/T			intron-variant	IFT122	GRCh38.p7	3:129454662	GGCTGTTGAGGAATG[A/C/T]GGGTCAGTCCAGGGC	55764
rs777407774	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129505233	GAATTGGACCAGTAC[C/T]TCTCTGACTGGGGAA	55764
rs777418707	snp	C/G	1.65312e-05	0.00287495	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478039	AAATGCAAAGAGCTT[C/G]TCAAGAAGATTGCCA	55764
rs777424590	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487880	GAGGGGCTTGGGAGG[A/G]CTCTGCAGAAGAGGT	55764
rs777435121	snp	A/G	1.64939e-05	0.0028717	missense, intron-variant	IFT122	GRCh38.p7	3:129461003	AAAACCAACCTGGCC[A/G]AAAGTGAGTCCCCAT	55764
rs777437054	snp	A/G	1.64958e-05	0.00287187	missense	IFT122	GRCh38.p7	3:129483561	GAGGAGGCTACCTCA[A/G]CATCAAAGCCAGCAC	55764
rs777441657	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129484268	CCTCCCGAATGCAGG[A/G]TGGTCTCCCCTCCAC	55764
rs777451153	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129509250	CACCCACTTATCAAG[-/C]TTTTTCACCTTCCCA	55764
rs777459038	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129483945	GGGAGGGGTATGCAG[A/T]GTTGTCAGCAGCGTG	55764
rs777470496	snp	C/T	2.6e-05	0.00360546	missense	IFT122	GRCh38.p7	3:129483647	AAGATCTTCTGCCTC[C/T]ATGTCTTCTCCATTT	55764
rs777485821	snp	A/C	0.000131796	0.00811668	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507683	ATCCTGCCCAGAAGG[A/C]CACAATGCTTGGCAA	55764
rs777522703	snp	A/G	1.64738e-05	0.00286995	stop-gained	IFT122	GRCh38.p7	3:129500060	TGGTGACCATGGCTG[A/G]GTTGACATGTAGGTT	55764
rs777568782	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511754	TGAGGAACTCCGCAT[A/G]TGTGCTCGTTTGGTG	55764
rs777572081	snp	A/G	0.000115305	0.00759205	missense	IFT122	GRCh38.p7	3:129499999	CCAAAGCCGCCGTGG[A/G]GATGTACATCTCAGC	55764
rs777602970	snp	A/C	1.65222e-05	0.00287417	synonymous-codon	IFT122	GRCh38.p7	3:129514488	CCTGTACATCCCTGC[A/C]AGATTCCAAAAGTCC	55764
rs777612170	snp	C/T	1.71593e-05	0.00292905	intron-variant	IFT122	GRCh38.p7	3:129488169	TGGGTAATCATCCCA[C/T]GCATCTGGAGGCAGG	55764
rs777645844	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464742	AGCGGCCGGGGGGCT[C/T]CCTCTCGCCAATATG	55764
rs777708111	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129489606	GCACTTTGGGAGGCC[A/G]AGGTGTGCGGATCAC	55764
rs777717739	snp	C/T	4.96742e-05	0.00498344	synonymous-codon	IFT122	GRCh38.p7	3:129514545	CGCCAAGCCCTTCCA[C/T]GACAGTGAGGTGAGG	55764
rs777744869	snp	A/G	9.88696e-05	0.00703029	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504433	AAAGGTAGGCAACAC[A/G]GACTGTCACCTTCTA	55764
rs777748806	in-del	-/AGTC			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475636	CAGCCTGGGCAACAG[-/AGTC]AGACCCTTTTTCAAA	55764
rs777796111	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129477320	AGCCCTAAGACTGCA[A/G]TCTCTCCCTCTGTCC	55764
rs777823931	snp	C/G	3.29647e-05	0.00405971	intron-variant	IFT122	GRCh38.p7	3:129452005	CGAAGGATGGTAAAA[C/G]GCTGCTCTGGGTTTC	55764
rs777842411	snp	A/T	1.64757e-05	0.00287012	intron-variant	IFT122	GRCh38.p7	3:129451879	TCTGACTAATAGATA[A/T]CACATAGATAATCTG	55764
rs777881964	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458185	ATTATTTGTCAAAAA[C/T]AAAAATTTAAGTAAA	55764
rs777888629	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129481767	CTTCCCAGTCCCTGC[A/G]GGAGGCTCTCCTGCT	55764
rs777888768	snp	A/G	1.6477e-05	0.00287024	intron-variant	IFT122	GRCh38.p7	3:129519061	TGGAGGCTAGGGTCT[A/G]TCTCCATCTCTGCTT	55764
rs777953704	in-del	-/TA	4.94931e-05	0.00497434	intron-variant	IFT122	GRCh38.p7	3:129469457	TGCAGTCATGCCTGT[-/TA]TATATTTTCATTTTC	55764
rs777977210	snp	A/G	1.65386e-05	0.00287559	synonymous-codon	IFT122	GRCh38.p7	3:129495466	GAAGAAGCGGGGAGA[A/G]ACCAACAATGACCTG	55764
rs778024080	snp	A/G	1.6477e-05	0.00287024	synonymous-codon	IFT122	GRCh38.p7	3:129519132	TCTGCGGCTAGTGGA[A/G]ACCAAGGACTCCATC	55764
rs778036488	in-del	-/CT			intron-variant	IFT122	GRCh38.p7	3:129469117	GGTCATAGCAGGGGA[-/CT]CAGTGAAACAGCAGA	55764
rs778043113	snp	G/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129506996	ACTGAAGGAGTAGTG[G/T]AAGTGGAAGAGACAA	55764
rs778053201	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129446506	AGGCATGAGCCACCG[C/T]GCCCGGCCGACCCTA	55764
rs778072425	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129472825	TGTTGTTCAGTATTA[A/G]ATTTCATTGACTCTT	55764
rs778094852	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129485407	CCATCATCCATGCCT[C/G]ACACAGATCAGCTAT	55764
rs778155003	snp	A/G			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438528	TATTGATAAAATTGA[A/G]TGACAGGTTAAATTA	55764
rs778160791	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129456950	GATACTATCTTAGTT[C/G]ACTCCCATAAAAAGA	55764
rs778165345	snp	A/G	1.64781e-05	0.00287033	synonymous-codon, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461282	TACTCATCAACTGGC[A/G]TCTTGTTCCTCCAGT	55764
rs778203224	snp	G/T	3.34292e-05	0.00408821	intron-variant	IFT122	GRCh38.p7	3:129502894	TGAGGTGAGGGGAAA[G/T]CAGGCCTCATGGGCT	55764
rs778206901	snp	A/G	3.29462e-05	0.00405857	missense	IFT122	GRCh38.p7	3:129488260	GAAATCCTGCAGTCC[A/G]CTCCCATGTACCAGT	55764
rs778250538	in-del	-/TGTGT			intron-variant	IFT122	GRCh38.p7	3:129465140	GTGTGTGTGTGTGTG[-/TGTGT]GTGTGTGTGTGTGTG	55764
rs778258261	snp	C/T	1.64836e-05	0.0028708	synonymous-codon	IFT122	GRCh38.p7	3:129502804	GGACAGCCCTGGCTA[C/T]GCTGCTGAGACCTAC	55764
rs778259085	snp	C/T	1.71331e-05	0.00292682	intron-variant	IFT122	GRCh38.p7	3:129514281	TTTCCTCTGCCTTCC[C/T]GGCACCAGCACAAGC	55764
rs778273588	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129456303	TTAGTATTTGCAGCA[A/C]TATCATATGGCTCAC	55764
rs778279982	snp	A/G	1.64754e-05	0.00287009	intron-variant	IFT122	GRCh38.p7	3:129476632	GACTTTCTCCAGAGA[A/G]CTGGGAATTGACAGT	55764
rs778283139	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129500917	TAACTGGCTAGTGCA[A/G]TAGAGCAGGAGGGAA	55764
rs778286258	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466834	CAGGATTTTAAATTA[C/T]AGTTTTAGTGTAGTT	55764
rs778289560	snp	C/T	9.70167e-05	0.00696412	upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129440287	GGTTGCTGAGACAGA[C/T]GCTGAGGCGGGTAGG	55764
rs778289843	snp	A/C	2.23536e-05	0.0033431	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439817	AGACTCAGACTCTCC[A/C]GCCCAGTCGTGCCCA	55764
rs778314263	in-del	-/C	1.6486e-05	0.00287102	intron-variant	IFT122	GRCh38.p7	3:129483462	TGGTTCTCACAGGAT[-/C]CCCCACTGTCCCTGT	55764
rs778330356	snp	C/T	3.29506e-05	0.00405884	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479791	GCTTCCTAGGAGAAA[C/T]GGCTGCAGTGCCTGT	55764
rs778333423	snp	C/T	1.64727e-05	0.00286986	stop-gained, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476456	GGGACTGTTGGGGAG[C/T]AGAACTCCTGGGTGT	55764
rs778449955	snp	C/T	3.65197e-05	0.004273	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520236	TGCTGCCCCTACTGC[C/T]GCAGGTGCAAGGATG	55764
rs778517139	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129513092	TGGGTGGGAGGGGCC[A/G]GAGAGGCAGCAGGAC	55764
rs778532487	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129443426	CTACAGTAGAATAGA[C/G]TGCCTGCAAATGAGT	55764
rs778534085	in-del	-/G	1.64762e-05	0.00287016	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476389	CGAGTACATTTTGCT[-/G]GGGGGTTCAGACAAG	55764
rs778550405	in-del	-/C	4.94482e-05	0.00497209	intron-variant	IFT122	GRCh38.p7	3:129488228	TCTGAAAACAGTCTT[-/C]CTTTTTTTCCCTTGA	55764
rs778570933	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129472952	TTTCCTTTTTATTCA[C/T]TACAAGCGTATTTTT	55764
rs778578197	snp	C/T	1.65334e-05	0.00287514	intron-variant	IFT122	GRCh38.p7	3:129499870	ACAGGAAGTTCTGAT[C/T]CAGAGTGTTTTTGTT	55764
rs778584430	snp	A/C	3.44762e-05	0.00415174	intron-variant	IFT122	GRCh38.p7	3:129467080	TTGTGAGTGTGTCCC[A/C]GTGAGTGGGAACCCT	55764
rs778597825	snp	C/T	6.58913e-05	0.00573945	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129469357	AGAGGAACGTAATGA[C/T]ATCCTGGCTGTGGCT	55764
rs778605933	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129519555	CTGTGCCTCCTTCCC[A/G]CCCACCCTGCAGCAA	55764
rs778606658	snp	C/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458411	TCTTTGTTTACTCAG[C/T]GTCAGACAAAGCAGG	55764
rs778607240	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129511870	AGGCTTATATGAATC[A/G]GTGGTTATGTCCTAA	55764
rs778625545	snp	A/G	3.29506e-05	0.00405884	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129451994	TGTGGCATATGCGAA[A/G]GATGGTAAAAGGCTG	55764
rs778631074	snp	A/C	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129506566	TGTGTAAACATCAGC[A/C]AGACCACTGTTTTCC	55764
rs778653148	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129462788	CTAGACATACACTTG[C/T]TATGAGGCACTGAGC	55764
rs778660165	snp	A/T	1.64751e-05	0.00287007	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129507669	GCTGCACACAGCAGA[A/T]CCTGCCCAGAAGGAC	55764
rs778712952	snp	C/T					GRCh38.p7	3:129496607	CACCACCTGTTCGAC[C/T]CTGGGGCTGAAGGTG	55764
rs778713165	snp	A/G					GRCh38.p7	3:129520597	CAACAGATTGCCTCA[A/G]TAATGACAAAAGGGC	55764
rs778713531	snp	G/T	1.78752e-05	0.00298953			GRCh38.p7	3:129515630	CTGAGCATGTGGGTG[G/T]GACAGCCTGTGGACA	55764
rs778752583	snp	G/T	1.65045e-05	0.00287263			GRCh38.p7	3:129476802	TCACTGAGCAGAAAG[G/T]TAAGAGGCAGGTCCA	55764
rs778846137	snp	C/T	4.94197e-05	0.00497066	missense, intron-variant	IFT122	GRCh38.p7	3:129460882	ATGTCTTCATTGCAC[C/T]TCCATCTTCCATTTC	55764
rs778888913	snp	C/G/T	0.000214805	0.0103614	missense, synonymous-codon	IFT122	GRCh38.p7	3:129514474	GACAAGCTGCGTGGC[C/G/T]TGTACATCCCTGCCA	55764
rs778908579	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129509256	CTTATCAAGCTTTTT[A/C]ACCTTCCCAATTTGC	55764
rs778928747	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464730	AAGTAAAGATCGAGC[A/G]GCCGGGGGGCTCCCT	55764
rs778941928	snp	C/T	3.30011e-05	0.00406195	missense	IFT122	GRCh38.p7	3:129519658	ATCAAGCGATGGCCC[C/T]CACCCCTGAGGTGGC	55764
rs778969921	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129493410	GCCTCATAACGTAAT[C/G]TGCTCTGTGCCACAT	55764
rs778970962	in-del	-/TGTC			intron-variant	IFT122	GRCh38.p7	3:129465066	TGTGTGTGGCGTGTG[-/TGTC]TGCGCACATGTGCAT	55764
rs779084080	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129490221	ATTGTGTACAACATG[-/C]TGTTTTGAAAAAGCC	55764
rs779098976	snp	C/G			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503657	ACTGTTGTCTGCTCT[C/G]TGAACAGCTCCATTG	55764
rs779103391	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464646	ACAGCTGGACAAATG[A/G]TGGTCAGTACCTGGC	55764
rs779124266	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482001	TGGGGCAATGACTCT[A/G]AGAGGGGTGTGACGT	55764
rs779127674	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468154	TGTCTCTTTTCCCTT[A/G]GTTTTGGGTTAGTGC	55764
rs779199906	snp	A/G	3.29462e-05	0.00405857	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504361	GAGTTTAAGGATGAC[A/G]TCTACATGCCGTATG	55764
rs779231460	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129473767	TACTCACCCAGCATG[A/G]TGGTGAAGAGGGCTG	55764
rs779231590	snp	G/T			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457095	TAAGATGTACAGAAT[G/T]TGGCACATACTTACC	55764
rs779236068	snp	C/T	1.65034e-05	0.00287253	synonymous-codon	IFT122	GRCh38.p7	3:129502738	CGCCCGCAAACTGGA[C/T]AAGGCTGAGCGCGAG	55764
rs779236550	snp	G/T	6.64507e-05	0.00576376	missense	IFT122	GRCh38.p7	3:129495454	TTTCCAGGAGAGGAA[G/T]AAGCGGGGAGAGACC	55764
rs779290112	snp	A/T	1.64751e-05	0.00287007	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504410	ACGATCGCTTTGAGG[A/T]AGCCCAGAAAGGTAG	55764
rs779291672	snp	G/T	1.64727e-05	0.00286986	splice-donor-variant, intron-variant	IFT122	GRCh38.p7	3:129492195	ATCAGCAGCATTGAG[G/T]TAAAAGATGAAGCAT	55764
rs779305111	snp	C/T	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129512263	TTTGGCCTGGCCCAG[C/T]AGCAGCTCTTGAAGA	55764
rs779311236	snp	G/T	1.64735e-05	0.00286993	intron-variant	IFT122	GRCh38.p7	3:129517638	TGTGCGGCTGTGTGA[G/T]GGGTCTGGGGACAGG	55764
rs779347932	snp	A/T	2.65396e-05	0.00364268	intron-variant	IFT122	GRCh38.p7	3:129461033	TCTCTACAAATAAGA[A/T]AACAGTGGGTGAGGA	55764
rs779382861	snp	A/G	3.30464e-05	0.00406474	missense	IFT122	GRCh38.p7	3:129514489	CTGTACATCCCTGCC[A/G]GATTCCAAAAGTCCA	55764
rs779388799	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129509352	GAGAGGATCAGCTTC[A/G]ATGATTGCTCTCGGT	55764
rs779395113	snp	A/G	1.64735e-05	0.00286993	missense	IFT122	GRCh38.p7	3:129512384	CTGCACAGCCTGCCC[A/G]AGGACACCCCCTCGG	55764
rs779410469	snp	A/G	3.37878e-05	0.00411008	missense	IFT122	GRCh38.p7	3:129481632	CGTAAGAAGCTGGCC[A/G]TGGTAGATGAAAATG	55764
rs779420817	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486780	ATCTCTCCTTTGCCC[A/G]TGGTAGCCTGAGCTG	55764
rs779429658	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129443384	GTATCTCTTTTATAA[A/G]AAGAGGCAGGTGGAG	55764
rs779465770	snp	C/T	1.66963e-05	0.00288927	intron-variant	IFT122	GRCh38.p7	3:129488194	GGCAGGCTCTGTATG[C/T]ATCTGGTTCTTTCCA	55764
rs779477942	in-del	-/TTGG	6.5893e-05	0.00573952	frameshift-variant	IFT122	GRCh38.p7	3:129488320	TACCAGATTGCTTGC[-/TTGG]GTGTCACAGACACTG	55764
rs779490228	snp	C/T			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441235	TTCTGGCCACTGGAG[C/T]AGGTTACTTGTCTTT	55764
rs779533417	snp	C/G	9.83889e-05	0.00701318	missense, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439794	TGGGGGCAGCTCCGC[C/G]GTCCCCCAGACTCAG	55764
rs779549926	snp	A/G	3.29554e-05	0.00405914	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129461268	TCCTACAATCCTATT[A/G]CTCATCAACTGGCAT	55764
rs779635761	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438687	GAAGTGGGAAGATCA[C/T]CTGATCCCAAGAGTT	55764
rs779655499	snp	C/T	1.6483e-05	0.00287076	missense	IFT122	GRCh38.p7	3:129502797	AGAAGCTGGACAGCC[C/T]TGGCTATGCTGCTGA	55764
rs779657090	snp	C/G	3.67782e-05	0.0042881	missense, utr-variant-3-prime	IFT122	GRCh38.p7	3:129520223	GCTTCAGCATGGCTG[C/G]TGCCCCTACTGCCGC	55764
rs779667589	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129502361	TGGAAATAATCATGC[C/T]CACCTCTTAGGGTGG	55764
rs779692994	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129464217	ATATCCCTTCCGTTC[A/G]GCATCTGTTGAGCAC	55764
rs779694237	snp	A/T	1.65943e-05	0.00288043	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478213	AATCACATCATCCTG[A/T]GCCAGGTGGGCAGCA	55764
rs779703788	snp	A/G	3.30251e-05	0.00406343	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458565	TGCTGGTTTAAGATA[A/G]ATGTAAGACTTTCCA	55764
rs779711516	snp	C/G	1.64792e-05	0.00287042	missense, utr-variant-5-prime, intron-variant	IFT122	GRCh38.p7	3:129458605	CACTTTTAGGCAAGC[C/G]CTTTGCTTCTGGATC	55764
rs779726490	snp	G/T	2.3603e-05	0.00343525	utr-variant-5-prime, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439880	GCGCCGCAACGCCCA[G/T]GGTGTGGGGCGGAGT	55764
rs779749855	in-del	-/A	1.64757e-05	0.00287012	splice-acceptor-variant, intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507663	CCACCCGCTGCACAC[-/A]GCAGATCCTGCCCAG	55764
rs779769935	in-del	-/AACA			intron-variant	IFT122	GRCh38.p7	3:129517300	ACACACACACACACA[-/AACA]CAGAGACTGCTCCTG	55764
rs779776838	snp	C/T	3.29451e-05	0.00405851	synonymous-codon	IFT122	GRCh38.p7	3:129506536	GTCCATGCAGTGCCT[C/T]GATATAGCTCAAGGT	55764
rs779780638	snp	C/G			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129475689	CATGGTGGCACTCAC[C/G]TATGGTCCCAGCTAC	55764
rs779783961	snp	A/G	1.64751e-05	0.00287007	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479785	GGGTTTGCTTCCTAG[A/G]AGAAACGGCTGCAGT	55764
rs779792513	snp	A/G	3.57891e-05	0.00423004	intron-variant	IFT122	GRCh38.p7	3:129515458	CACGTGCCTGCCCCG[A/G]CCCCTCGGGAGTCCG	55764
rs779837916	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129451046	TTTTAAACTCTCCAC[A/G]TAGTGATAGATGTCA	55764
rs779845322	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129513284	ACATAATTGTCCCTG[G/T]TCTTTTCTAAATCTC	55764
rs779847148	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129499896	TTGTTTGTTGTGCTT[-/C]CTCAGGATTTCCTTG	55764
rs779862475	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516051	CAGAAACTGCCCCTG[-/CA]CACACACACACAGAC	55764
rs779898200	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129466616	AAGCAATCCTCTCAC[C/T]TCAGCCTCCCAAGTA	55764
rs779926427	snp	C/G	1.64732e-05	0.0028699	synonymous-codon	IFT122	GRCh38.p7	3:129499985	AAATATCAAGGAGCC[C/G]AAAGCCGCCGTGGAG	55764
rs779977478	snp	A/G	8.2411e-05	0.00641862	intron-variant	IFT122	GRCh38.p7	3:129495644	CCAAGCTCCAGCTTG[A/G]AGCCCACTGGTATTC	55764
rs779994717	snp	A/G	1.67354e-05	0.00289265	intron-variant, missense	IFT122	GRCh38.p7	3:129467059	GACAGTCCCAGGGAC[A/G]ACAACTTGTGAGTGT	55764
rs780007247	snp	A/G	1.65553e-05	0.00287705	missense	IFT122	GRCh38.p7	3:129519572	CCACCCTGCAGCAAG[A/G]TGGCTCAGAGTTCGT	55764
rs780011126	snp	G/T	1.6473e-05	0.00286988	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129466977	GGAAATCCCTTCCAC[G/T]CTGAAGTCAGCAGTG	55764
rs780029099	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129478707	CCTGTCCAGCTTCCT[A/G]AAGTACTGGGATTAT	55764
rs780062386	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129452219	CTTGAGTTACTTCAG[A/C]GAAAAAAACGGTGGT	55764
rs780083815	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129485816	GGCCATCCTGCTGAC[G/T]CAGCGGGTCAGGACT	55764
rs780088435	snp	A/G	1.66194e-05	0.00288261	intron-variant	IFT122	GRCh38.p7	3:129488425	CCAGCAGGAGCTGGA[A/G]TTTGGTCCTTGTGGG	55764
rs780092044	snp	C/T	0.000207663	0.0101877	intron-variant	IFT122	GRCh38.p7	3:129459279	GAACAGATACTGCAT[C/T]TATTTTTTGTTTTGT	55764
rs780092665	snp	C/G	1.64727e-05	0.00286986	intron-variant	IFT122	GRCh38.p7	3:129464601	TGTGGGGTGCTTCCC[C/G]TATCCCCATGCCTTT	55764
rs780093208	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129501068	CCATTCGTCAAGGTG[C/G]ACAACAGGGAGAGGA	55764
rs780141465	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129510307	TGTGCTGACTTCTCA[A/G]CACATTTTTTGCCTC	55764
rs780152864	snp	C/T	1.64779e-05	0.00287031	missense	IFT122	GRCh38.p7	3:129483533	CAGTGTGAGGACATG[C/T]TCTGCTTCTCGGGAG	55764
rs780214139	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129509811	GGCTAGTATGTTGGT[A/T]TAGTGGGTAAACTCG	55764
rs780228738	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476668	CACCCCGCAGGTGGT[C/T]GGCTGCCAGGACGGC	55764
rs780230790	in-del	-/C	0.000100155	0.00707585	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440414	AGGAGGTCGAGTCCT[-/C]CGCGGGGAGTGCGCG	55764
rs780297062	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129490218	TCTATTGTGTACAAC[A/G]TGCTGTTTTGAAAAA	55764
rs780334455	snp	C/T	1.65329e-05	0.0028751	missense	IFT122	GRCh38.p7	3:129514424	CCAAGCAGAGCAAGG[C/T]CCTCGGTGCCTACAG	55764
rs780336050	snp	A/G	1.6609e-05	0.0028817	intron-variant	IFT122	GRCh38.p7	3:129517429	GGCAAGTCCTTTGCA[A/G]GGCCTCCAGCCCCCT	55764
rs780355403	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129506301	GATGCTCCAATGAGT[A/G]TCCTACTTCCAAAGC	55764
rs780364592	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129446928	GTAGTAACCTTAACA[A/G]TAGTCTGTTTTGACA	55764
rs780366618	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129460376	AGGCTCATCTGTGTT[A/G]TAGCATGTGTCAGAA	55764
rs780369719	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129496822	CACCTAGAAGATTTC[A/G]TAACACATTCATACT	55764
rs780370898	snp	A/C	4.94189e-05	0.00497062	missense, downstream-variant-500B	IFT122	GRCh38.p7	3:129504340	GCTTTGGGTGAGAAG[A/C]ATCCTGAGTTTAAGG	55764
rs780383178	in-del	-/A			intron-variant	IFT122	GRCh38.p7	3:129479256	GACCCCATCTCCACC[-/A]AAAAAAAAAAAAAAA	55764
rs780406640	snp	C/T	1.65304e-05	0.00287488	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129507787	CTGGGTCACCAGCAC[C/T]TGAGGGTACCATCTC	55764
rs780453712	snp	A/T	4.94376e-05	0.00497156	intron-variant	IFT122	GRCh38.p7	3:129479964	AGGCTGATAATCTGC[A/T]TGCACACGTGGGTGA	55764
rs780464202	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129494500	TTAAAACTTTCACCA[C/G]CTTGTCTAAGAGTTT	55764
rs780476179	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464716	AAATGGCGAGGAGAA[A/G]GTAAAGATCGAGCGG	55764
rs780486776	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129513018	CAAGTGGATGTTCCA[A/G]GGGAGGACCCAGCAT	55764
rs780582816	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129486529	CTCATTGTGTGCTTT[A/C]AGAAAAGCTTTCAGG	55764
rs780586191	snp	C/G/T	4.95506e-05	0.00497727	missense, synonymous-codon	IFT122	GRCh38.p7	3:129502858	CCTGGTGCAGCTGCA[C/G/T]GTGGAGACCCAGCGC	55764
rs780597767	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459027	TCAGAAACTTGGGGT[C/T]AGTGTGCTCCAGGCC	55764
rs780605044	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129518274	CAGCTCAGCCTGCCC[A/C]TTGGCCAGGAGGATG	55764
rs780608076	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129470336	TGGCTCAGTCTTGGC[C/T]CACTGCAAGCTCCGC	55764
rs780637283	snp	A/G	1.64741e-05	0.00286998	intron-variant	IFT122	GRCh38.p7	3:129500072	CTGGGTTGACATGTA[A/G]GTTTTGGTCCCTGCC	55764
rs780651091	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129482165	GAAGGGGATGGGCAA[A/G]CCTGGCCTTCTACTT	55764
rs780651863	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129479987	GTGGGTGACCCGTCT[A/G]GCAATGACTCTGAGC	55764
rs780701511	snp	A/C	3.41734e-05	0.00413347	intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129476289	CGGAAATGGTTTTTC[A/C]CTTGCTGTGTGTTCT	55764
rs780708661	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129502510	ACACAAGGTGGCTGA[C/G]AGGATCCTGTAAAGG	55764
rs780741348	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129483043	ATTCTCAGCCCTGCC[A/G]GGAGACATCAGCATT	55764
rs780789530	snp	A/G	1.65679e-05	0.00287814	synonymous-codon	IFT122	GRCh38.p7	3:129514554	CTTCCACGACAGTGA[A/G]GTGAGGATGCAGCAC	55764
rs780807337	snp	A/G			intron-variant, missense	IFT122	GRCh38.p7	3:129503542	AATCCATCCCCGAGA[A/G]GATTAGGAGCTGTGC	55764
rs780812247	in-del	-/CATT			intron-variant	IFT122	GRCh38.p7	3:129453982	ATAACATTGAGATAA[-/CATT]CTGTAGCCACTGCCA	55764
rs780817724	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	IFT122	GRCh38.p7	3:129512353	TGAAACTCTTTTCAA[C/T]ATCTCCAGGTTCCTG	55764
rs780884643	snp	C/T	0.000172436	0.00928377	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	MBD4, IFT122	GRCh38.p7	3:129439750	GTCATTCGGCGGGTC[C/T]GGGACTAGGCGCTCA	55764
rs780916009	snp	C/T	3.31433e-05	0.0040707	intron-variant, synonymous-codon	IFT122	GRCh38.p7	3:129519777	GCTTCTCTTGGCCAC[C/T]TTTCCCTTGCCCAAA	55764
rs780939018	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129468093	ATCAGTGCCAGTCAC[A/G]CAAAGGTCATCTGCA	55764
rs780944047	snp	G/T	4.94752e-05	0.00497344	intron-variant	IFT122	GRCh38.p7	3:129452015	TAAAAGGCTGCTCTG[G/T]GTTTCCATTCTCTAT	55764
rs780949756	snp	A/G	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129488172	GTAATCATCCCACGC[A/G]TCTGGAGGCAGGCTC	55764
rs780991214	in-del	-/T	1.6473e-05	0.00286988	intron-variant	IFT122	GRCh38.p7	3:129512296	TCAATCCCTGTTTGC[-/T]TTTCTCTCACTGCAG	55764
rs781006994	snp	C/T	0.000398406	0.0141083	synonymous-codon	IFT122	GRCh38.p7	3:129483667	CTTCTCCATTTCTGC[C/T]GTGGAGGTGCCGCAG	55764
rs781010380	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129510467	CTGAAACGAGACCCC[C/G]TCAGGGTCCCTCATC	55764
rs781014344	in-del	-/GC			intron-variant	IFT122	GRCh38.p7	3:129516168	ACAGAGACCGCCCCT[-/GC]GCACACACACACACA	55764
rs781020535	snp	C/T	0.000180986	0.00951105	intron-variant	IFT122	GRCh38.p7	3:129515456	GACACGTGCCTGCCC[C/T]GGCCCCTCGGGAGTC	55764
rs781026677	snp	A/G	3.29946e-05	0.00406155	intron-variant, downstream-variant-500B	IFT122	GRCh38.p7	3:129504460	TCTAGAAGGAGCAGG[A/G]GAAGTTACTGCCAAG	55764
rs781028876	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129453183	GATGGGATCTAGGGC[A/G]TAGACGGGGTATTTG	55764
rs781045697	snp	C/T			missense	IFT122	GRCh38.p7	3:129481669	GCCTGGTGTATGACA[C/T]CGACACCAAGGAGCT	55764
rs781080869	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129505362	GCCCTCTCTGGACAC[A/G]TTGCAGAACAAATGT	55764
rs781098526	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129509704	TCTACTATCAAACAG[C/G]AAATTCCAGAGCCAA	55764
rs781116538	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	IFT122	GRCh38.p7	3:129506449	AGAAGCGGTCCAGGT[A/G]CTGGAGCAGCTCACA	55764
rs781127638	snp	C/T	1.64798e-05	0.00287047	intron-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129479768	AATTTCCATGCAGAG[C/T]TGGGTTTGCTTCCTA	55764
rs781136638	snp	C/T	1.6473e-05	0.00286988	intron-variant, missense	IFT122	GRCh38.p7	3:129466958	TTGTCAACAGATATA[C/T]TCAGGAAATCCCTTC	55764
rs781138540	snp	A/G	1.64738e-05	0.00286995	missense	IFT122	GRCh38.p7	3:129495569	GAGAACCTCGCGCTT[A/G]AAATGTACACCGACC	55764
rs781181264	snp	A/G	0.000115368	0.00759412	missense, utr-variant-5-prime	IFT122	GRCh38.p7	3:129478162	AAGGAGAAGATTATC[A/G]AGAAGTTTGAGTGCA	55764
rs781204826	snp	A/G			upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129441466	TCTAAGGTAGGTACT[A/G]TAATTTCCTCTATTT	55764
rs781249205	snp	A/G	1.64866e-05	0.00287106	missense	IFT122	GRCh38.p7	3:129502829	ACCTACCTGAAGATG[A/G]GTGACCTCAAGTCCC	55764
rs781338240	snp	A/G	1.648e-05	0.0028705	synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129458603	AACACTTTTAGGCAA[A/G]CGCTTTGCTTCTGGA	55764
rs781362276	snp	C/T	1.64762e-05	0.00287016	missense	IFT122	GRCh38.p7	3:129519146	AGACCAAGGACTCCA[C/T]CGGAGATGAGGACCC	55764
rs781375120	snp	A/G	3.30808e-05	0.00406686	missense	IFT122	GRCh38.p7	3:129481671	CTGGTGTATGACATC[A/G]ACACCAAGGAGCTGC	55764
rs781376398	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516566	CAGATTGCTCCTGCA[-/CA]CACACACACACAGAG	55764
rs781409395	snp	A/G	9.88321e-05	0.00702896	synonymous-codon, utr-variant-5-prime	IFT122	GRCh38.p7	3:129476476	CTCCTGGGTGTGGAC[A/G]TGTCAAGCGAAACCG	55764
rs781426818	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129478543	CACTGCAGCTTTGAC[C/T]TCCCAAGCTCAAGCG	55764
rs781451037	snp	C/G	1.65567e-05	0.00287716	synonymous-codon	IFT122	GRCh38.p7	3:129514410	ACTCTTCACCTTGGC[C/G]AAGCAGAGCAAGGCC	55764
rs781483806	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129459638	TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTTC	55764
rs781529023	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129498033	ACACTGTTTAGTCTC[A/G]TTCATCACTCAGCAC	55764
rs781578865	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129471237	CAGCTTTTGGGCCAT[C/T]TCTTCTACCCCTGCC	55764
rs781581045	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129444732	TCACCATGTTGGCCA[A/G]GATGGTCTCCATCTC	55764
rs781585961	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129449459	TTTCCCTGAGGGGAG[G/T]GAGGGATTATGATCT	55764
rs781593272	snp	A/T	1.65833e-05	0.00287948	intron-variant	IFT122	GRCh38.p7	3:129519563	CCTTCCCGCCCACCC[A/T]GCAGCAAGGTGGCTC	55764
rs781606792	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129519539	TGGCTGAGTGAGGAC[A/G]CTGTGCCTCCTTCCC	55764
rs781612599	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129483155	TCTCATTATAAAAAA[C/T]AATCCATGCTGATTA	55764
rs781635627	snp	C/G/T	3.29491e-05	0.00405877	missense	IFT122	GRCh38.p7	3:129479881	GTGATCGGTGGCCCT[C/G/T]CTGGAAGAGAAGGCC	55764
rs781644020	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129514998	CAGCTTCCTTCTTTC[A/G]CACATCCTCCCTCAA	55764
rs781661959	in-del	-/CTTT			intron-variant	IFT122	GRCh38.p7	3:129459776	TTCCTTCCTTCCTTT[-/CTTT]CTTTTCAGTCTTGCT	55764
rs781675973	snp	C/T	3.31686e-05	0.00407225	intron-variant	IFT122	GRCh38.p7	3:129488414	TAAGCATCTAGCCAG[C/T]AGGAGCTGGAGTTTG	55764
rs781681195	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129469780	TACTTTCCTCTATTC[A/G]CTTTCTTTCATTCAA	55764
rs781700869	snp	C/T	1.65608e-05	0.00287752	intron-variant	IFT122	GRCh38.p7	3:129463533	TTCCAACCAATCCAT[C/T]TTCTTTTATATTATT	55764
rs781713912	snp	C/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129438858	AGGACTGCTTAAGTC[C/T]GGCAGGTCAAGGCTT	55764
rs781733102	snp	C/T	5.75545e-05	0.00536413	synonymous-codon	IFT122	GRCh38.p7	3:129515568	CTGCATCAACTGCCG[C/T]CAGCCCTTCATCTTC	55764
rs781759897	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129506094	GAGCAGGGGGCAGAA[-/C]CTCACTGAAGATGAG	55764
rs781762618	in-del	-/AGT	0.000102192	0.00714742	upstream-variant-2KB, intron-variant	MBD4, IFT122	GRCh38.p7	3:129440422	CGAGTCCTCGCGGGG[-/AGT]GCGCGAGCCGCTGCA	55764
rs781766922	in-del	-/G	1.64743e-05	0.00287	frameshift-variant, utr-variant-5-prime	IFT122	GRCh38.p7	3:129464769	TATGGTCCATCTGCT[-/G]GAACCCTTCAAGGTA	55764
rs786205566	snp	G/T			missense	IFT122	GRCh38.p7	3:129483546	TGCTCTGCTTCTCGG[G/T]AGGAGGCTACCTCAA	55764
rs786205567	snp	C/T			splice-donor-variant	IFT122	GRCh38.p7	3:129500070	GGCTGGGTTGACATG[C/T]AGGTTTTGGTCCCTG	55764
rs794727330	snp	A/T			missense	IFT122	GRCh38.p7	3:129499938	CCCAAAGAAACAAAG[A/T]TGCTAATCACCAAAC	55764
rs794727536	snp	C/T			synonymous-codon	IFT122	GRCh38.p7	3:129519642	CCGCCGGGATGTCCT[C/T]ATCAAGCGATGGCCC	55764
rs794727737	snp	A/T			missense, intron-variant	IFT122	GRCh38.p7	3:129460920	CCACAAAACAGTAAG[A/T]GTAACAGCCACAGAT	55764
rs796081569	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129492355	GGGCAGAGTGGCCAC[A/G]CTGGGGGAGACAACA	55764
rs796084675	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129508691	ACTTTGGGATTTGAC[A/G]AACTCTTGGAAAGCA	55764
rs796124284	snp	G/T			intron-variant, upstream-variant-2KB	MBD4, IFT122	GRCh38.p7	3:129439348	AAAGTCTCGGTAAAA[G/T]ACTCTGTAAAAAGAA	55764
rs796141073	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129491373	CCACCTGAAAGCAGC[C/T]TGACCTGGTGGCTTG	55764
rs796257627	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129493912	CGTTAAAGTAAACTC[C/G]TAAGATTGTCTCTTG	55764
rs796259060	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129465787	AGCTGGGACTACAGG[C/T]GCCCGCCACCGCGCC	55764
rs796289558	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129480248	ATTTCTAGAGGGAGG[C/G]AGAGATCGTTACCTA	55764
rs796357199	snp	G/T			intron-variant	IFT122	GRCh38.p7	3:129465644	CCTGGCTAATTTTTT[G/T]TTTTTTTTTGAGACG	55764
rs796369490	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129512632	CAGGGCTCTCTGAGC[C/T]GAACCCAGCAGTGGG	55764
rs796377772	snp	C/T			intron-variant, utr-variant-3-prime	IFT122	GRCh38.p7	3:129503647	GAGCCGTCTGACTGT[C/T]GTCTGCTCTCTGAAC	55764
rs796387422	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129468349	CTAGGAATGCTTTTC[-/T]TTTTTTTTTTTTGTG	55764
rs796388316	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129486546	GAAAAGCTTTCAGGA[A/G]TTTGAGAAAGCTTCC	55764
rs796395244	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129472727	CATTAGACCTTTTGT[-/T]ACTGTTCTCCAAGTC	55764
rs796412296	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129514211	AAATTCCTGGGCCTT[C/G]CCATCCGAGAAGTAC	55764
rs796455382	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129465780	CCCGAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA	55764
rs796456720	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129514186	AACTACGCTGTTTTT[A/C]TCTTTGGAAAAATTC	55764
rs796493840	snp	C/G			intron-variant	IFT122	GRCh38.p7	3:129492796	TTGCTGGGTGGTGGT[C/G]AACACTATGCTTTTT	55764
rs796553443	in-del	-/GCCCCTGCACACACACATGGAGACT			intron-variant	IFT122	GRCh38.p7	3:129516461	ACACACACAGAGACC[-/GCCCCTGCACACACACATGGAGACT]GCCCCTGCACACACA	55764
rs796559880	in-del	-/C			intron-variant	IFT122	GRCh38.p7	3:129478273	TTTGTGCTCCCCCCC[-/C]AGTGATAGGGTGCCC	55764
rs796608147	in-del	-/CACA			intron-variant	IFT122	GRCh38.p7	3:129516287	CACAGATTGCTCCTG[-/CACA]CACACACACACACAC	55764
rs796626001	snp	A/C			intron-variant, upstream-variant-2KB	IFT122	GRCh38.p7	3:129457816	TCTCGGCTCACTGCA[A/C]GCCCCACCTCCTGGG	55764
rs796626574	snp	A/T			intron-variant	IFT122	GRCh38.p7	3:129470289	TTTTTTTCGAGATGG[A/T]GTCTCACTCTGTGGC	55764
rs796641446	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129497237	CACGCCACTGCATTC[C/T]AGCCTGGGTGACAGA	55764
rs796699593	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129467302	AGAAAGTTCAACTTT[-/T]CTGATAAAACCCCAT	55764
rs796701061	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129454803	TGTCAGAGTGTGACC[C/T]ATCAGTAGTGGCATT	55764
rs796751357	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129505134	ACTTAACCTATGTAA[A/C]CTTGAATCTTGCCAA	55764
rs796756041	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129496412	CCTTCCATCAAGGGG[C/T]TTTGTTAACCTGCCT	55764
rs796798398	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516170	CAGAGACCGCCCCTG[-/CA]CACACACACACAGAA	55764
rs796818384	multinucleotide-polymorphism	AC/GT			intron-variant	IFT122	GRCh38.p7	3:129487971	CAAAGGCATTCCAGG[AC/GT]AGGGTGACATCCTAT	55764
rs796863626	in-del	-/AG			intron-variant	IFT122	GRCh38.p7	3:129517302	CACACACACACACAC[-/AG]AGACTGCTCCTGCAC	55764
rs796866200	snp	A/G			intron-variant	IFT122	GRCh38.p7	3:129487979	ATTCCAGGTGAGGGT[A/G]ACATCCTATGGCGAG	55764
rs796878919	snp	C/T			intron-variant	IFT122	GRCh38.p7	3:129516251	GCCCCTGCGTGCACA[C/T]ACAGACTGCCCCTAC	55764
rs796913300	in-del	AA/T			intron-variant	IFT122	GRCh38.p7	3:129496395	GGCAATGAGGGTCTT[AA/T]CTTCCATCAAGGGGC	55764
rs796926120	in-del	-/TTCC			intron-variant	IFT122	GRCh38.p7	3:129459634	TCCTTCCTTCCTTCC[-/TTCC]CTCCCTCCCTCCCTT	55764
rs796929682	in-del	ACGCCTGGCTAATTTTTTGTTGCCACCACACCT/GCGCCC			intron-variant	IFT122	GRCh38.p7	3:129465798	AGGCGCCCGCCACCG[lengthTooLong]GCTAATTTTTTGTAT	55764
rs796932600	in-del	-/CA			intron-variant	IFT122	GRCh38.p7	3:129516754	CTGCACACACACACA[-/CA]GACTGCCCCTGCACA	55764
rs796965730	snp	A/C			intron-variant	IFT122	GRCh38.p7	3:129478534	ATTATGGCTCACTGC[A/C]GCTTTGACCTCCCAA	55764
rs796999830	in-del	-/T			intron-variant	IFT122	GRCh38.p7	3:129450012	TCTGAAATTTGACCC[-/T]TTTTTTTTTTTTTTG	55764
rs797013749	in-del	-/CACACACA			intron-variant	IFT122	GRCh38.p7	3:129516695	CACAGATTGCTCCTG[-/CACACACA]CACACACACACACAC	55764

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