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

ANKRD13B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs753244876	snp	A/T	1.65644e-05	0.00287783	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608973	CAGCGAGGGAACCGC[A/T]GCTTTGTCTTCAGGG	124930
rs753304981	in-del	-/CAT	1.77963e-05	0.00298292	intron-variant	ANKRD13B	GRCh38.p7	17:29607924	CCGGGGCCTCCCCAG[-/CAT]CATAGACCTATGGTT	124930
rs753338763	snp	C/G/T	3.33385e-05	0.00408269	intron-variant	ANKRD13B	GRCh38.p7	17:29612020	AAGTGAGGCCCCTGC[C/G/T]GGTGCTGGGAAGGTG	124930
rs753427592	snp	A/C	1.66203e-05	0.00288268	intron-variant	ANKRD13B	GRCh38.p7	17:29609017	AGGCAGGAAGTGGGG[A/C]AGGGTGGGGACGATG	124930
rs753574234	snp	G/T	1.67156e-05	0.00289093	intron-variant	ANKRD13B	GRCh38.p7	17:29609077	CCTGTGCTGTTCCGT[G/T]TCTGGCAGACACAAG	124930
rs753610009	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29601283	CTGGAGTGCAGTGGT[A/G]CGATCTCTGTTCACT	124930
rs753657977	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604401	TTTTGTAGACATGGG[A/G]TTTTGGTATGTTGCC	124930
rs753764117	snp	A/C	1.75579e-05	0.00296288	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607772	CTGGATCCCCGCGGC[A/C]GGACTCCCCTGCACC	124930
rs753915573	snp	C/G	3.34314e-05	0.00408835	intron-variant	ANKRD13B	GRCh38.p7	17:29608273	GGTCGCTTCTGGGCT[C/G]TCCCACTTTAGGTCC	124930
rs753981831	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595311	GCCAGCCTCTGCTGG[C/G]TCTTCTCTGCTTTCC	124930
rs754009715	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609902	CCTTTATCCCTAAAA[A/G]TGACTGCCTGGCTGG	124930
rs754029689	snp	C/G	1.87542e-05	0.00306214	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612632	CCCGGCCGTGCCTGA[C/G]CCAGCCCCCGCGCCC	124930
rs754047222	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29597289	TGTTCCTGTGCAAAT[-/A]ACGCACACACACGTT	124930
rs754059646	snp	C/T	0.000434391	0.0147312	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612512	AGCGAGACGCCTTCC[C/T]CAGGCAGCGACTCCT	124930
rs754077939	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29594898	TCGGACTGAGCAGGC[G/T]GGGGGTCAGGATGTG	124930
rs754079725	snp	A/G	1.68618e-05	0.00290356	splice-donor-variant	ANKRD13B	GRCh38.p7	17:29609276	TATCTCCTTTGAGAG[A/G]TGGGTGGACATGGCC	124930
rs754297614	snp	A/T	1.65449e-05	0.00287614	intron-variant	ANKRD13B	GRCh38.p7	17:29611555	GGAGTTGCGGTGTCC[A/T]CTGAGATGCCACATT	124930
rs754344267	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601224	CCCAGCCTGACATTC[-/T]TTTTTTTTTTTTTTT	124930
rs754523455	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602046	ATTTCTTGGTTCTTG[A/G]CTTTATCTTGGTATT	124930
rs754540447	snp	A/G	1.67385e-05	0.00289292	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609086	TTCCGTGTCTGGCAG[A/G]CACAAGCGCCGTGGT	124930
rs754555763	snp	A/G	1.66186e-05	0.00288254	intron-variant	ANKRD13B	GRCh38.p7	17:29609018	GGCAGGAAGTGGGGC[A/G]GGGTGGGGACGATGG	124930
rs754838274	snp	A/T	1.75486e-05	0.0029621	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607775	GATCCCCGCGGCCGG[A/T]CTCCCCTGCACCTGG	124930
rs754894713	snp	C/T	1.7719e-05	0.00297644	intron-variant	ANKRD13B	GRCh38.p7	17:29611858	GGGAGCTCCTGGGCC[C/T]CTCCCCATGTGGTAC	124930
rs755061035	snp	A/G	1.68616e-05	0.00290353	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612522	CTTCCCCAGGCAGCG[A/G]CTCCTCCAGCGTCAG	124930
rs755188538	snp	C/T	1.86967e-05	0.00305745	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612633	CCGGCCGTGCCTGAC[C/T]CAGCCCCCGCGCCCC	124930
rs755285692	snp	A/G	1.67315e-05	0.00289231	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610757	GAACAGCACAAGGGC[A/G]AGGTCAAAGGTAATG	124930
rs755304230	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29596477	TCCTGGTTCTGGAGT[C/G]GTGAGTTCCTGGTGT	124930
rs755340913	snp	A/G	1.69499e-05	0.00291112	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608070	AGCGGGTGGTGAAGC[A/G]GCTGGCGGGCATCCC	124930
rs755375303	snp	C/T	1.65384e-05	0.00287557	intron-variant	ANKRD13B	GRCh38.p7	17:29611562	CGGTGTCCTCTGAGA[C/T]GCCACATTTCTTGTA	124930
rs755680004	snp	C/G	1.65916e-05	0.00288019	missense, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611991	GCCCCATGGAACTGA[C/G]CACCAAGACACAGAA	124930
rs755686225	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29608299	GTCCTGCGCTTGCTC[-/A]CCCTGCCTGGAATGT	124930
rs755694171	snp	A/C/T	0.000195348	0.00988131	intron-variant	ANKRD13B	GRCh38.p7	17:29611856	AGGGGAGCTCCTGGG[A/C/T]CCCTCCCCATGTGGT	124930
rs755748963	snp	C/T	3.34633e-05	0.0040903	intron-variant	ANKRD13B	GRCh38.p7	17:29608835	CAAAGCCACCTCCAA[C/T]CTCCGCTTCCACCAG	124930
rs755885987	snp	A/C	1.68633e-05	0.00290368	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609170	CTGGGCAGGACCGGG[A/C]GCTGCTGCTGGCTGC	124930
rs755888127	snp	C/T	5.26219e-05	0.00512915	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612499	AGGCAGCCCCAGCAG[C/T]GAGACGCCTTCCCCA	124930
rs755943053	snp	C/G	1.68153e-05	0.00289955	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609250	GTCACCACTCAGCTT[C/G]ACACCAAGAATATCT	124930
rs756228670	in-del	-/AC			intron-variant	ANKRD13B	GRCh38.p7	17:29605417	TATACACACACAAAC[-/AC]ACACACACACACACA	124930
rs756237354	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591894	GGCGGGAGAAAGGGG[C/T]GAGGCAGCCCGCTCC	124930
rs756260079	snp	A/G	3.71678e-05	0.00431075	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612369	AGGTGTGAGGGGCTG[A/G]GTGGTGGCGCCTAAA	124930
rs756326128	snp	C/T	1.689e-05	0.00290598	intron-variant	ANKRD13B	GRCh38.p7	17:29608131	GCCCAGCCTCTCAGC[C/T]TCCACGGGAGCCCTT	124930
rs756427362	snp	A/G	1.96219e-05	0.00313218	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612845	GCGCGCGGGGCCACG[A/G]GACTCCGCGCCGCCA	124930
rs756484273	snp	G/T	1.82881e-05	0.00302385	intron-variant	ANKRD13B	GRCh38.p7	17:29610659	GACCAGAACTGCTTA[G/T]GAGCCCTTTCTTCAT	124930
rs756549314	snp	A/G	2.75775e-05	0.00371322	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612974	GACAGGTCAGTGCCC[A/G]CTGGGCCGGAGAGAA	124930
rs756604431	snp	A/G	6.66223e-05	0.00577119	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610743	CAGAACATCTTTCAG[A/G]ACAGCACAAGGGCAA	124930
rs756625885	in-del	-/C	4.99405e-05	0.00499677	intron-variant	ANKRD13B	GRCh38.p7	17:29612013	GACACAGAAGTGAGG[-/C]CCCTGCCGGTGCTGG	124930
rs756698235	snp	A/G	1.66966e-05	0.00288929	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608040	TGCAGCTGGTGCTTC[A/G]GTACCGGGACTACCA	124930
rs756846804	snp	A/G	3.06396e-05	0.00391393	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613515	AGCAGGAGGAGAGGC[A/G]GCGGCGCGCGCGCCA	124930
rs756866813	snp	A/G	3.3042e-05	0.00406447	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611584	TTTCTTGTAGGCTGT[A/G]AGACACCTTTGCAGT	124930
rs756892352	snp	C/T	0.000146316	0.00855201	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593773	GCGGGGACCCCGCGG[C/T]CGGGCACGCCCGTCC	124930
rs756917681	snp	C/G	1.65814e-05	0.00287931	intron-variant	ANKRD13B	GRCh38.p7	17:29608175	GTGCAGACTTAGCCT[C/G]TCTCCCCTTCGTCCT	124930
rs756920015	snp	A/G	1.78099e-05	0.00298406	intron-variant	ANKRD13B	GRCh38.p7	17:29611843	GCATTAGGAACTGAG[A/G]GGAGCTCCTGGGCCC	124930
rs756950260	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615205	GTGTAGCCACTGGGT[C/T]CGGCTCTGCAGCAAA	124930
rs756950321	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29596952	GCGGTCCCCACAGCC[C/T]GTGGCCTCCTACGCA	124930
rs757046151	snp	A/G	1.80932e-05	0.0030077	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612360	CTGAGGCTGAGGTGT[A/G]AGGGGCTGAGTGGTG	124930
rs757078276	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604416	GTTTTGGTATGTTGC[C/T]CAGGCTGGTCTTGAA	124930
rs757079363	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605390	ATATTTTCTATATAG[A/G]GAAATATATATATAT	124930
rs757091231	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605981	GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	124930
rs757320704	snp	A/C	0.000768991	0.0195935	intron-variant	ANKRD13B	GRCh38.p7	17:29607905	GCTCACCCCAGCCCC[A/C]CAGCCGGGGCCTCCC	124930
rs757397266	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595371	ATGTGGGAAGAACTT[C/T]CCAGGGGTCCAAGGA	124930
rs757424469	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29594917	GGTCAGGATGTGTCT[C/G]TGAAGTCCCACGCTG	124930
rs757504519	snp	A/G	1.67323e-05	0.00289239	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608026	GGACCTGGAGCTGGT[A/G]CAGCTGGTGCTTCGG	124930
rs757768430	snp	C/T	1.96891e-05	0.00313754	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612840	CGCGGGCGCGCGGGG[C/T]CACGGGACTCCGCGC	124930
rs757887091	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29609281	CCTTTGAGAGGTGGG[C/T]GGACATGGCCTTGGT	124930
rs757978866	snp	C/T	3.91474e-05	0.00442404	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612995	CCGGAGAGAATCCTC[C/T]GGAGAGGATCCTGTC	124930
rs758029701	in-del	-/GT	4.97055e-05	0.00498501	intron-variant	ANKRD13B	GRCh38.p7	17:29611531	TGATGAGGTGCCCAG[-/GT]GTGTGTGTGGAGTTG	124930
rs758052836	snp	C/T	1.67354e-05	0.00289265	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609135	CCGCCGGGTGGTGTA[C/T]ACAGAGACTCTGGCA	124930
rs758060233	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606190	TGCTGGGATTACAGG[C/T]GTGAGCTACCGCGCC	124930
rs758170371	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29608291	CCACTTTAGGTCCTG[C/T]GCTTGCTCCCCTGCC	124930
rs758229252	snp	A/C	1.64849e-05	0.00287092	missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612208	TGGCCGTCAGCAATG[A/C]GCTTTTTGCCAAGCT	124930
rs758262349	snp	C/G/T	0.000166982	0.00913593	intron-variant	ANKRD13B	GRCh38.p7	17:29612035	CGGTGCTGGGAAGGT[C/G/T]GGGGGCCGGGGCTCC	124930
rs758373365	snp	A/G	1.66432e-05	0.00288467	intron-variant	ANKRD13B	GRCh38.p7	17:29609029	GGGCAGGGTGGGGAC[A/G]ATGGGAGGCAGCCCC	124930
rs758423328	snp	A/G	1.67624e-05	0.00289498	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609094	CTGGCAGACACAAGC[A/G]CCGTGGTCATGGAGA	124930
rs758452197	snp	C/G	1.7009e-05	0.0029162	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609409	GGAGATGGTGAATGG[C/G]TATGAAGCTAAGGTG	124930
rs758469179	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29606591	AAACAAACAAAACTT[-/A]ACGTTTAACAAACAT	124930
rs758501197	snp	C/T	1.7521e-05	0.00295976	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607786	CCGGACTCCCCTGCA[C/T]CTGGCCACCACGCTG	124930
rs758505113	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598831	GCTGGGATTACAGAC[C/G]TGAGCCCCCCGGCAT	124930
rs758541697	snp	C/T	1.75708e-05	0.00296397	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612653	CCCCGCGCCCCCAGC[C/T]TCCTGCCGCGGCTGC	124930
rs758653403	snp	A/G	0.000145919	0.00854038	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607874	AATCGCAGCGGCTGG[A/G]CAGGTGGGCAGCCCT	124930
rs758721594	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610346	GAAGGCCTCTGTGCT[A/T]CCCCCACCAGTGCAT	124930
rs758782712	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601632	GAACTCCCTTTAACA[-/T]TTCCTGCACATCTGG	124930
rs758909363	snp	A/C	7.54802e-05	0.00614284	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612528	CAGGCAGCGACTCCT[A/C]CAGCGTCAGCAGCTC	124930
rs758994654	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29611377	CTTTTAGTGTTTTAA[A/G]CTGTGCTCACAGAGG	124930
rs759020556	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595663	TCAGAAACAAGGTCC[C/T]AGATTCACCCCTACC	124930
rs759024250	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595036	GGTCTGGGTGGCCAC[C/T]TCCTGTTACCTGTGC	124930
rs759158852	snp	C/T	4.94499e-05	0.00497217	synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612164	TCCCCTGTCCCTGTG[C/T]GAGCAGGTGGCCCCC	124930
rs759214286	in-del	-/TTC			cds-indel, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615167	AAAGAAGGAAGAGAG[-/TTC]TCTACCACAGACCGC	124930
rs759217031	snp	G/T	1.67172e-05	0.00289108	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612310	TCCTGAGCCCGTGGC[G/T]GGCCGACCGGGGTTT	124930
rs759217528	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29603710	CTTACTATCTTTAGA[C/T]GGTCCACTGGGTTCT	124930
rs759232329	snp	C/G	1.6743e-05	0.0028933	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609126	TGACCACGACCGCCG[C/G]GTGGTGTACACAGAG	124930
rs759444785	snp	A/C	5.72088e-05	0.005348	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612881	AACGCCCACGCCTCC[A/C]CGCAGGTCACCATCT	124930
rs759500555	snp	A/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599172	GAGAAAGCTTTGGGG[A/C]TCTCTGGAGGATCCT	124930
rs759580279	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607263	TGTATTACTGTAACC[A/G]TTTGTTAAACCTCAC	124930
rs759647543	in-del	-/G	0.000657678	0.018122	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593901	AAAGGGTGATCCCCT[-/G]CCGGCCGGGACGGGC	124930
rs759692406	snp	C/G	5.75291e-05	0.00536295	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612777	CTGCAATTCGCCATC[C/G]AGCAGAGCCTGCTTG	124930
rs759716622	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601175	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGCTT	124930
rs759722370	snp	C/T	8.28246e-05	0.00643471	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608970	TGGCAGCGAGGGAAC[C/T]GCAGCTTTGTCTTCA	124930
rs759903357	snp	A/C			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615024	TCTTGTTTTTCTGAG[A/C]GAGGCAACGGCAGAG	124930
rs759966152	snp	C/T	1.67525e-05	0.00289413	intron-variant	ANKRD13B	GRCh38.p7	17:29608277	GCTTCTGGGCTCTCC[C/T]ACTTTAGGTCCTGCG	124930
rs759989180	snp	A/G	1.6525e-05	0.00287441	intron-variant	ANKRD13B	GRCh38.p7	17:29611684	AGTGGAGGGATGTGG[A/G]TGTGGCTCAGGAGGA	124930
rs760035170	snp	A/G	1.78004e-05	0.00298327	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607745	CTCCTCCTCCAGGTG[A/G]ACATCGAGCAGCTGG	124930
rs760042793	snp	C/T	1.65583e-05	0.00287731	synonymous-codon, missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611962	CTTTGAGCTGGGCAA[C/T]CGTGATATGGGCCGC	124930
rs760158552	snp	C/T	7.01582e-05	0.00592235	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607840	GCTCCTGGCGCACGG[C/T]GCAGACGTGGGCAGG	124930
rs760272637	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605465	ATATATACACACACA[C/T]GCATATGTATATATA	124930
rs760354824	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611123	TTGCCACAGATTCTG[C/T]ATGCCCATTGATGCC	124930
rs760386544	snp	A/G	1.64879e-05	0.00287118	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612145	TGTGGCTGTGTGAGG[A/G]GCATCCCCTGTCCCT	124930
rs760491217	in-del	-/GAC	0.000358012	0.0133745	cds-indel, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612744	GAGGCGGCGACCCGG[-/GAC]GACGACGACGACCTG	124930
rs760502252	snp	G/T	0.000684931	0.0184931	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612620	GGGAGGGGCGCGCCC[G/T]GCCGTGCCTGACCCA	124930
rs760765253	in-del	-/A	1.80127e-05	0.003001	intron-variant	ANKRD13B	GRCh38.p7	17:29607894	TGGGCAGCCCTGCTC[-/A]CCCCAGCCCCACAGC	124930
rs760876081	snp	C/T	3.30442e-05	0.0040646	intron-variant	ANKRD13B	GRCh38.p7	17:29611665	GTGTGCAGGGGTACC[C/T]GTAAGTGGAGGGATG	124930
rs760959256	snp	A/G	3.336e-05	0.00408398	intron-variant	ANKRD13B	GRCh38.p7	17:29608262	GGGCTGCAGCAGGTC[A/G]CTTCTGGGCTCTCCC	124930
rs761010732	snp	C/G	1.65551e-05	0.00287702	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608937	GACACCACACTCCTG[C/G]GCTTTGACCACATGA	124930
rs761046981	snp	C/T	2.47118e-05	0.00351501	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613472	TACGACGAGCAGCTG[C/T]GGCTGGCGATGGAAC	124930
rs761098279	snp	A/G	9.9346e-05	0.00704721	intron-variant	ANKRD13B	GRCh38.p7	17:29611548	TGTGTGTGGAGTTGC[A/G]GTGTCCTCTGAGATG	124930
rs761130140	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601404	TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA	124930
rs761243477	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29608521	AGTCCTGTCTTTTTC[A/G]CTGTTGTATTCCCAG	124930
rs761340883	in-del	-/C	1.70335e-05	0.00291829	intron-variant	ANKRD13B	GRCh38.p7	17:29608122	CAAGGTGAGGCCCAG[-/C]CTCTCAGCCTCCACG	124930
rs761534372	snp	C/G	1.76971e-05	0.0029746	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607754	CAGGTGGACATCGAG[C/G]AGCTGGATCCCCGCG	124930
rs761553685	snp	A/G	1.75203e-05	0.00295971	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607831	TGCCCGTGTGCTCCT[A/G]GCGCACGGCGCAGAC	124930
rs761631702	in-del	-/GTCA	2.3087e-05	0.00339749	splice-donor-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612963	TCGCCGACAGGACAG[-/GTCA]GTCAGTGCCCGCTGG	124930
rs761749280	snp	A/G	0.0364458	0.129979	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612608	CCCGGGGTGGGTGGG[A/G]GGGGCGCGCCCGGCC	124930
rs761757012	snp	C/G	1.65573e-05	0.00287721	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608213	CAGGACTTCTACGTG[C/G]AGATGAAATGGGAGT	124930
rs761766289	snp	A/G/T	5.10608e-05	0.0050525	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612495	TGCGAGGCAGCCCCA[A/G/T]CAGCGAGACGCCTTC	124930
rs761782852	snp	G/T	2.14218e-05	0.00327268	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612954	CCTACGAGGGTCGCC[G/T]ACAGGACAGGTCAGT	124930
rs761821310	snp	C/G	1.68035e-05	0.00289853	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609240	CGCGCCCGTCGTCAC[C/G]ACTCAGCTTGACACC	124930
rs762020530	snp	C/T	3.32773e-05	0.00407892	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610724	CTCATCACCCGCACA[C/T]GGACAGAACATCTTT	124930
rs762077672	snp	C/T	1.65701e-05	0.00287833	intron-variant	ANKRD13B	GRCh38.p7	17:29611529	CTCTGATGAGGTGCC[C/T]AGGTGTGTGTGGAGT	124930
rs762126840	snp	A/T	1.70394e-05	0.0029188	intron-variant	ANKRD13B	GRCh38.p7	17:29608120	CGCAAGGTGAGGCCC[A/T]GCCTCTCAGCCTCCA	124930
rs762128942	snp	A/G	1.65141e-05	0.00287346	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611643	GGGCCCCCAAAATGG[A/G]GTGAGTGTGTGCAGG	124930
rs762150989	snp	C/T	1.65644e-05	0.00287783	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612291	GAGACCGCACGGCCA[C/T]TTCTCCTGAGCCCGT	124930
rs762200480	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600330	ATCAGGTGGCAGGCT[A/G]GCCTGTTCATTGTAG	124930
rs762254067	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29603332	CTGCAGCCTCGAACT[A/C]CTGGGCTCAAGGGAT	124930
rs762305016	snp	C/T	3.34348e-05	0.00408855	intron-variant	ANKRD13B	GRCh38.p7	17:29609074	CCCCCTGTGCTGTTC[C/T]GTGTCTGGCAGACAC	124930
rs762432887	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592811	CCGGATCCTTCTTCA[C/T]GGCCCCTGGGACCCA	124930
rs762441170	snp	G/T	0.000106245	0.00728776	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612472	CTGCGACGAACCGGT[G/T]CCATCGGTGCGAGGC	124930
rs762495118	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591657	CCCCGTGGAGATGTC[A/G]CCACCCCAGGAAGCA	124930
rs762573093	snp	A/C			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594393	GCTGAGGGGCCCTGG[A/C]TGCTGGAAGGACTTG	124930
rs762597237	in-del	-/GGTG	0.00012078	0.00777017	intron-variant	ANKRD13B	GRCh38.p7	17:29613304	GTCCCGGCCCCGGCC[-/GGTG]GGTGGGTGGGTGCGC	124930
rs762676086	snp	A/G	1.68168e-05	0.00289967	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609232	CGGCTTACCGCGCCC[A/G]TCGTCACCACTCAGC	124930
rs762716597	snp	A/G	6.87191e-05	0.0058613	intron-variant	ANKRD13B	GRCh38.p7	17:29607974	CTGTGACCTTGCCTC[A/G]CCCTCCCCCAGTGCT	124930
rs762727498	snp	A/G	5.35776e-05	0.00517551	synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593711	CCGCCACCGCGAGCT[A/G]GAGAAGGAGGTCCGC	124930
rs762829997	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29608627	AAATGATGGACACTA[C/G]GGACTTAGTGGTGAC	124930
rs762869944	snp	G/T	1.7219e-05	0.00293414	intron-variant	ANKRD13B	GRCh38.p7	17:29610789	GGCAGAGCTGGATGG[G/T]GAGAGGTGTTGCAGG	124930
rs762923291	snp	C/T	1.72133e-05	0.00293366	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608091	CGGGCATCCCCGTGC[C/T]CCTGGAGAAGCTGCG	124930
rs762940025	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614759	AAGAGGCTTCATACC[A/G]GAGGCTTTTGCTACC	124930
rs762964059	snp	A/G	1.67371e-05	0.0028928	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612319	CGTGGCGGGCCGACC[A/G]GGGTTTAGATGAGGT	124930
rs763086734	snp	C/G	0.000330191	0.0128447	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611628	CGCTGAGCAGCACGG[C/G]GGCCCCCAAAATGGG	124930
rs763142304	snp	G/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597790	TGCATGGGGTGTATG[G/T]GGTGCTGAGCCATCC	124930
rs763222866	snp	C/T	3.69693e-05	0.00429922	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612913	GGAGGCGCTAACCAA[C/T]AGCAAGCCAGGCACC	124930
rs763229298	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598873	TTCTGCAATGATTTC[C/T]TGGTTAATTACCTTC	124930
rs763257890	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29604288	ATCTCAGCTCATTGC[A/C]GCCTCAACCTCCTGG	124930
rs763344660	snp	A/G	3.31384e-05	0.00407039	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611976	ACCGTGATATGGGCC[A/G]CCCCATGGAACTGAC	124930
rs763397835	snp	A/G	1.65392e-05	0.00287564	intron-variant, missense, utr-variant-3-prime	ANKRD13B	GRCh38.p7	17:29612100	TCCCTTACCCCTTGG[A/G]ATCTGGTGGGGGCAG	124930
rs763399687	snp	C/T	1.65699e-05	0.00287831	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608981	GAACCGCAGCTTTGT[C/T]TTCAGGGGCCAAGGT	124930
rs763443627	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605474	CACACACGCATATGT[A/G]TATATATATTTGAGA	124930
rs763633319	snp	A/G	7.9466e-05	0.00630291	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612481	ACCGGTGCCATCGGT[A/G]CGAGGCAGCCCCAGC	124930
rs763670922	snp	C/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609160	CTGGCACTGGCTGGG[C/G]AGGACCGGGAGCTGC	124930
rs763775140	snp	A/G	0.000166099	0.00911164	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593721	GAGCTGGAGAAGGAG[A/G]TCCGCGCGGGCCAGG	124930
rs763817114	snp	C/T	8.61438e-05	0.00656235	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608092	GGGCATCCCCGTGCT[C/T]CTGGAGAAGCTGCGC	124930
rs763889908	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595819	CTCCTTCCCTCAGGC[A/G]TGCCAAAAAGAGGAA	124930
rs763999078	snp	A/G	0.0001789	0.00945612	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612355	TGGGGCTGAGGCTGA[A/G]GTGTGAGGGGCTGAG	124930
rs764060127	in-del	-/C	1.80302e-05	0.00300246	intron-variant	ANKRD13B	GRCh38.p7	17:29607895	GGGCAGCCCTGCTCA[-/C]CCCAGCCCCACAGCC	124930
rs764113953	snp	A/G	1.88592e-05	0.00307071	intron-variant	ANKRD13B	GRCh38.p7	17:29610643	GTAAGACACAGGGTA[A/G]GACCAGAACTGCTTA	124930
rs764182681	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604201	TACTTGCAAATCAGT[C/T]TGACCTTTTTGAGGC	124930
rs764270322	snp	C/T	1.8745e-05	0.0030614	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612929	AGCAAGCCAGGCACC[C/T]ACCCCATGTCCTACG	124930
rs764376141	snp	A/G/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599340	GTAACACTTCACAGG[A/G/T]TGACTTTAGCTGCCA	124930
rs764387130	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29609887	GACCCTAGAGCCAGG[C/T]CTTTATCCCTAAAAA	124930
rs764464930	snp	C/T	1.66441e-05	0.00288474	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610718	GTGGAGCTCATCACC[C/T]GCACACGGACAGAAC	124930
rs764470406	snp	C/T	1.65809e-05	0.00287926	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608990	CTTTGTCTTCAGGGG[C/T]CAAGGTCAGGCAGGC	124930
rs764619213	in-del	-/CCCCAGGCCA	1.66674e-05	0.00288676	intron-variant	ANKRD13B	GRCh38.p7	17:29609041	GACGATGGGAGGCAG[-/CCCCAGGCCA]CCCCTGATCCCCCTG	124930
rs764818306	snp	A/G	1.64833e-05	0.00287078	missense, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612171	TCCCTGTGTGAGCAG[A/G]TGGCCCCCATCATTG	124930
rs764873442	snp	C/T	1.67242e-05	0.00289168	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612313	TGAGCCCGTGGCGGG[C/T]CGACCGGGGTTTAGA	124930
rs764926539	snp	A/G	1.67379e-05	0.00289287	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609129	CCACGACCGCCGGGT[A/G]GTGTACACAGAGACT	124930
rs765050919	snp	A/G	1.90054e-05	0.00308259	intron-variant	ANKRD13B	GRCh38.p7	17:29610637	TTAGGGGTAAGACAC[A/G]GGGTAAGACCAGAAC	124930
rs765146394	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607401	CCACCCCACTTCAGT[C/T]CCAGGCTTATTCTTG	124930
rs765198237	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605999	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	124930
rs765206512	snp	C/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614319	ACTCCCTCATGGTGC[C/G]TCGGAGAGTGGGGAG	124930
rs765230316	snp	A/G	4.96964e-05	0.00498455	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608971	GGCAGCGAGGGAACC[A/G]CAGCTTTGTCTTCAG	124930
rs765238346	snp	C/T	0.000254745	0.0112831	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612634	CGGCCGTGCCTGACC[C/T]AGCCCCCGCGCCCCC	124930
rs765368401	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611282	CCCCACAGTGCCTGC[C/T]GGGGCAGGCGTTTTA	124930
rs765454264	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29603484	TGGGCTGGTCTTAAA[C/T]TCCTGAACTCAAGCC	124930
rs765497284	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598691	GGAGCTAGGACTACA[A/G]GTGGTGCCACCATGC	124930
rs765506823	snp	A/T			missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593680	AGTATCCGCTGCACT[A/T]CCTCGTGTGGCACAA	124930
rs765517093	in-del	-/AAACAAAC			intron-variant	ANKRD13B	GRCh38.p7	17:29606561	AGACTCTGTCTCAAA[-/AAACAAAC]AAACAAACAAACAAA	124930
rs765536287	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29596212	CTGAGGAGGGGGCCA[A/G]CATGGCCACCTTCAG	124930
rs765555619	snp	A/G	1.91122e-05	0.00309124	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612797	GAGCCTGCTTGAGGC[A/G]GGCAGTGAGTATGAC	124930
rs765581016	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600358	TAGGGTCACCAGATG[C/T]CTGTATTCTGAGGTC	124930
rs765622978	snp	A/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597617	TTCCAGCAATTAAAT[A/T]GCTAGAGGCCTCTGC	124930
rs765679822	snp	A/G	1.65575e-05	0.00287724	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611964	TTGAGCTGGGCAACC[A/G]TGATATGGGCCGCCC	124930
rs765690807	snp	A/C/T	3.55021e-05	0.00421308	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607750	CCTCCAGGTGGACAT[A/C/T]GAGCAGCTGGATCCC	124930
rs765779506	in-del	-/C			intron-variant	ANKRD13B	GRCh38.p7	17:29594641	TCATGGCAGAGATGA[-/C]CCCCCCGCCTCCAGG	124930
rs765872387	snp	A/G	1.75634e-05	0.00296334	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607843	CCTGGCGCACGGCGC[A/G]GACGTGGGCAGGGAG	124930
rs765916532	snp	A/G	1.66596e-05	0.00288609	intron-variant	ANKRD13B	GRCh38.p7	17:29612018	AGAAGTGAGGCCCCT[A/G]CCGGTGCTGGGAAGG	124930
rs765958314	in-del	-/CCC	3.87845e-05	0.00440349	cds-indel, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613388	CAGCGCCAGCCTGCG[-/CCC]CCGGCGTCAGTGCCC	124930
rs766005708	snp	C/G	1.64833e-05	0.00287078	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612159	GAGCATCCCCTGTCC[C/G]TGTGTGAGCAGGTGG	124930
rs766140264	snp	C/G	1.9783e-05	0.00314501	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612623	AGGGGCGCGCCCGGC[C/G]GTGCCTGACCCAGCC	124930
rs766193676	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29611173	CCAGATACCGTGTCC[A/G]AGGTGAAAAAGCATA	124930
rs766392813	snp	C/G	0.000100215	0.00707797	intron-variant	ANKRD13B	GRCh38.p7	17:29608269	AGCAGGTCGCTTCTG[C/G]GCTCTCCCACTTTAG	124930
rs766394847	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598891	GTTAATTACCTTCCC[C/T]TCCTTGTGCCCCCTC	124930
rs766420136	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597848	TGTGGGGATGGGGAG[A/G]AGCACCCTGCTTGCA	124930
rs766563769	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29600637	GGGGACCAGGGGATC[A/C]TGAATTGTAACCAGC	124930
rs766652555	snp	C/T	0.000499708	0.0157989	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612504	GCCCCAGCAGCGAGA[C/T]GCCTTCCCCAGGCAG	124930
rs766734204	snp	A/G	2.48988e-05	0.00352829	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613473	ACGACGAGCAGCTGC[A/G]GCTGGCGATGGAACT	124930
rs766767416	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611401	ACAGAGGCCCTGGCC[C/T]CTGGTCCTTGAAGCA	124930
rs766816883	snp	C/T	0.000314169	0.0125294	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593697	CTCGTGTGGCACAAC[C/T]GCCACCGCGAGCTGG	124930
rs766905448	snp	C/T	3.70398e-05	0.00430331	intron-variant	ANKRD13B	GRCh38.p7	17:29607695	GCTCCGGAGGGCTGC[C/T]TCCGACGTGACTGGG	124930
rs766968377	snp	C/G	1.65542e-05	0.00287695	intron-variant	ANKRD13B	GRCh38.p7	17:29611549	GTGTGTGGAGTTGCG[C/G]TGTCCTCTGAGATGC	124930
rs767072406	snp	A/G	1.76216e-05	0.00296825	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607761	ACATCGAGCAGCTGG[A/G]TCCCCGCGGCCGGAC	124930
rs767230669	snp	A/C			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591808	GCTGCAGCCACGACA[A/C]TCTGCTGACCCCTGG	124930
rs767262258	snp	C/T	1.7782e-05	0.00298173	intron-variant	ANKRD13B	GRCh38.p7	17:29611850	GAACTGAGGGGAGCT[C/T]CTGGGCCCCTCCCCA	124930
rs767302083	snp	C/G	5.1336e-05	0.0050661	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612496	GCGAGGCAGCCCCAG[C/G]AGCGAGACGCCTTCC	124930
rs767341781	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605401	ATAGAGAAATATATA[C/T]ATATACACACACAAA	124930
rs767408184	snp	G/T	1.68086e-05	0.00289896	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609246	CGTCGTCACCACTCA[G/T]CTTGACACCAAGAAT	124930
rs767471409	snp	C/G	0.000183807	0.00958486	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613407	CGGCGTCAGTGCCCA[C/G]CCCTCGGCCCAGCTC	124930
rs767498463	snp	C/T	0.000692281	0.018592	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612618	GTGGGAGGGGCGCGC[C/T]CGGCCGTGCCTGACC	124930
rs767679107	snp	A/C	1.66358e-05	0.00288402	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610728	TCACCCGCACACGGA[A/C]AGAACATCTTTCAGA	124930
rs767736220	snp	A/G	8.28288e-05	0.00643487	intron-variant	ANKRD13B	GRCh38.p7	17:29611532	TGATGAGGTGCCCAG[A/G]TGTGTGTGGAGTTGC	124930
rs767736334	snp	C/T	1.66983e-05	0.00288944	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608038	GGTGCAGCTGGTGCT[C/T]CGGTACCGGGACTAC	124930
rs767787140	snp	A/C	1.70252e-05	0.00291759	intron-variant	ANKRD13B	GRCh38.p7	17:29608122	CAAGGTGAGGCCCAG[A/C]CTCTCAGCCTCCACG	124930
rs767945543	snp	A/G	5.02542e-05	0.00501244	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609122	AGATTGACCACGACC[A/G]CCGGGTGGTGTACAC	124930
rs768077242	snp	G/T	0.00033162	0.0128725	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612603	CTCTCCCCGGGGTGG[G/T]TGGGAGGGGCGCGCC	124930
rs768133799	snp	A/G	2.21134e-05	0.00332509	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612958	CGAGGGTCGCCGACA[A/G]GACAGGTCAGTGCCC	124930
rs768232540	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29608364	CTTAGCTCAGCTCAG[C/G]GCCACCGCCTCAGCT	124930
rs768233725	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607262	GTGTATTACTGTAAC[C/T]GTTTGTTAAACCTCA	124930
rs768293314	snp	C/G	3.88176e-05	0.00440537	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612683	CGAGATCTCCCCAGC[C/G]TTGTTCGAGGCCCCG	124930
rs768367015	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29597362	TGCATGTGCTTGTAC[A/G]CTTAAGGGCACACGT	124930
rs768512998	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613973	CACTAACCCCACTCC[A/G]GGACACTGCCCCTGA	124930
rs768537542	snp	C/T	0.000272067	0.0116602	intron-variant	ANKRD13B	GRCh38.p7	17:29610809	GGTGTTGCAGGACTG[C/T]GGGAACCAGCTCCCA	124930
rs768567187	snp	C/T	3.31109e-05	0.00406871	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608209	GGCCCAGGACTTCTA[C/T]GTGGAGATGAAATGG	124930
rs768590713	snp	A/G	1.65132e-05	0.00287339	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611626	ATCGCTGAGCAGCAC[A/G]GGGGCCCCCAAAATG	124930
rs768637612	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592725	AGACCCCTGGCTGCT[C/T]CAATGACCCTTGGTA	124930
rs768666787	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604824	CTGGGATTACAGGCA[G/T]GAGCCACTGCACCCG	124930
rs768681319	snp	G/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598609	GCTGGAGTGCAGTAG[G/T]GTGATCACAGCTCAG	124930
rs768717872	snp	C/T	5.03859e-05	0.005019	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609117	CATGGAGATTGACCA[C/T]GACCGCCGGGTGGTG	124930
rs768739778	in-del	-/GAC	0.000358012	0.0133745	cds-indel, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612743	GAGGCGGCGACCCGG[-/GAC]GACGACGACGACGAC	124930
rs768771017	snp	G/T	1.68502e-05	0.00290255	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609179	ACCGGGAGCTGCTGC[G/T]GGCTGCTGCTCAGCC	124930
rs768775763	snp	C/T	2.0058e-05	0.00316679	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612396	TAAAGGTTTCCTCAT[C/T]CTCAGAAATCCCGAT	124930
rs768822966	in-del	-/AAAC			intron-variant	ANKRD13B	GRCh38.p7	17:29606565	TCTGTCTCAAAAAAC[-/AAAC]AAACAAACAAACAAA	124930
rs768824029	snp	C/G	0.000479271	0.0154728	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593658	GCCAGGAAGGGGCCC[C/G]AGGGCAAGTATCCGC	124930
rs768984716	snp	C/G/T	8.27704e-05	0.00643266	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612285	ATTGGTGAGACCGCA[C/G/T]GGCCATTTCTCCTGA	124930
rs769054503	snp	A/G	9.2285e-05	0.0067922	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613377	CGCCCACGCCGCAGC[A/G]CCAGCCTGCGCCCCC	124930
rs769055486	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595177	GTGGGTCACAGTGCC[C/T]CCAGGAAACAGATGA	124930
rs769094235	snp	G/T	1.65244e-05	0.00287436	intron-variant, missense, utr-variant-3-prime	ANKRD13B	GRCh38.p7	17:29612108	CCCTTGGGATCTGGT[G/T]GGGGCAGGTTCAAGG	124930
rs769122853	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600322	GTAAGGTGATCAGGT[A/G]GCAGGCTGGCCTGTT	124930
rs769178879	snp	C/T	8.25552e-05	0.00642424	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611613	GTCCTTCCTGGGAAT[C/T]GCTGAGCAGCACGGG	124930
rs769341184	snp	C/T	1.65663e-05	0.002878	intron-variant	ANKRD13B	GRCh38.p7	17:29608185	AGCCTCTCTCCCCTT[C/T]GTCCTCCAGGCCCAG	124930
rs769372897	snp	C/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592543	AGCTGCCACCTGCTG[C/G]TTTTTCTGTCCAACC	124930
rs769448371	snp	A/C	3.69747e-05	0.00429953	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612909	TCTGGGAGGCGCTAA[A/C]CAACAGCAAGCCAGG	124930
rs769516438	snp	A/G	6.26056e-05	0.00559454	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612464	CTCAACGGCTGCGAC[A/G]AACCGGTGCCATCGG	124930
rs769519351	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29594087	CCCGAGTGAGGGTGC[C/G]GAGGTGGGAAAGGCT	124930
rs769586524	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602489	CTTCCAAAGGCTCTA[-/G]GGGAAGAGTCCTGCC	124930
rs769656587	snp	C/G	0.000124727	0.00789608	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613044	AGCCGGAGAACCCGC[C/G]GGGCCCTCGGCAGGG	124930
rs769707849	snp	A/G	1.71437e-05	0.00292772	intron-variant	ANKRD13B	GRCh38.p7	17:29610784	AATGAGGCAGAGCTG[A/G]ATGGGGAGAGGTGTT	124930
rs769752561	snp	C/G			synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610756	AGAACAGCACAAGGG[C/G]AAGGTCAAAGGTAAT	124930
rs769863180	snp	C/G	1.66749e-05	0.00288741	intron-variant	ANKRD13B	GRCh38.p7	17:29612049	TGGGGGGCCGGGGCT[C/G]CAGGAGATGCTGGGA	124930
rs769933936	snp	C/G	1.67638e-05	0.0028951	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609100	GACACAAGCGCCGTG[C/G]TCATGGAGATTGACC	124930
rs770252850	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29603326	AGCTCACTGCAGCCT[C/T]GAACTCCTGGGCTCA	124930
rs770330525	snp	C/T	3.50036e-05	0.00418337	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607820	CACCTTGAGTGTGCC[C/T]GTGTGCTCCTGGCGC	124930
rs770340905	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606980	GCTTGAACCTGGGAG[A/G]CGGAGGTTACAGCGA	124930
rs770423173	snp	C/G	1.71625e-05	0.00292933	intron-variant	ANKRD13B	GRCh38.p7	17:29610679	CCTTTCTTCATCTGT[C/G]CCCAGGTGTATGGGG	124930
rs770455865	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595624	GCTGCTCATGTGTTT[C/G]TCTCTCCCACCCCTC	124930
rs770478222	snp	A/G	1.68584e-05	0.00290326	intron-variant	ANKRD13B	GRCh38.p7	17:29610769	GGCAAGGTCAAAGGT[A/G]ATGAGGCAGAGCTGG	124930
rs770535423	snp	A/G	1.71728e-05	0.00293021	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608079	TGAAGCGGCTGGCGG[A/G]CATCCCCGTGCTCCT	124930
rs770623621	snp	A/G	3.33495e-05	0.00408333	intron-variant	ANKRD13B	GRCh38.p7	17:29609046	TGGGAGGCAGCCCCA[A/G]GCCACCCCTGATCCC	124930
rs770662738	snp	C/G	2.22314e-05	0.00333394	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612733	GCGGCCAGCGGGAGG[C/G]GGCGACCCGGGACGA	124930
rs770717814	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614953	CTCGTTCCCCTCACT[C/T]CCACCCATGCAGGAG	124930
rs770845057	snp	A/C/T	3.81703e-05	0.00436852	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612880	TAACGCCCACGCCTC[A/C/T]CCGCAGGTCACCATC	124930
rs770925792	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29609505	TGACCTCCCTTCCCC[A/C]GCCCTGGAGGTACAG	124930
rs770944356	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29610191	AGCGAGACTCCATCT[-/A]AAAAAAAAAAAAAAA	124930
rs770995646	snp	C/T	6.67791e-05	0.00577798	intron-variant	ANKRD13B	GRCh38.p7	17:29612041	TGGGAAGGTGGGGGG[C/T]CGGGGCTCCAGGAGA	124930
rs771066018	snp	A/G	9.93147e-05	0.0070461	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611946	AATACTTCAACCCCA[A/G]CTTTGAGCTGGGCAA	124930
rs771079478	in-del	-/CCCCTCCGGCC			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593897	CCGGGAAAGGGTGAT[-/CCCCTCCGGCC]GGGACGGGCGGGACC	124930
rs771084263	in-del	-/CGCCC	1.65514e-05	0.0028767	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612282	AGATTGGTGAGACCG[-/CGCCC]CACGGCCATTTCTCC	124930
rs771118809	snp	A/G	1.65567e-05	0.00287716	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608951	GGGCTTTGACCACAT[A/G]ACCTGGCAGCGAGGG	124930
rs771360885	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606977	ATCGCTTGAACCTGG[A/G]AGACGGAGGTTACAG	124930
rs771475263	snp	A/G	1.69689e-05	0.00291275	intron-variant	ANKRD13B	GRCh38.p7	17:29609304	GCCTTGGTCACCCTT[A/G]AGCCAGCCCGGTGGG	124930
rs771504698	snp	C/T	1.81447e-05	0.00301198	intron-variant	ANKRD13B	GRCh38.p7	17:29609465	CAGCTGCACTCTTGC[C/T]TACAGCAAGCTGTAC	124930
rs771538905	snp	C/T	2.93958e-05	0.00383367	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612699	TTGTTCGAGGCCCCG[C/T]GCGGCTACAGCATGA	124930
rs771592128	snp	C/T	1.95234e-05	0.00312431	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612856	CACGGGACTCCGCGC[C/T]GCCACGGCTAACGCC	124930
rs771616495	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600118	CCTGACCTCGTGATC[C/T]GCCCACCTCGGCCTC	124930
rs771687136	snp	C/T	1.76717e-05	0.00297247	intron-variant	ANKRD13B	GRCh38.p7	17:29610669	GCTTATGAGCCCTTT[C/T]TTCATCTGTCCCCAG	124930
rs771782795	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29610867	TGGCATCCTAGCAAG[A/G]GGCTGGATGCTTTAT	124930
rs771986393	snp	A/G	1.66693e-05	0.00288693	intron-variant	ANKRD13B	GRCh38.p7	17:29608258	AAGCGGGCTGCAGCA[A/G]GTCGCTTCTGGGCTC	124930
rs771990046	snp	A/C	1.65806e-05	0.00287924	missense, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611922	ACCCCACTGCCATCA[A/C]TGCAGAAGAATACTT	124930
rs772034182	snp	C/T	0.000315607	0.012558	synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593669	GCCCGAGGGCAAGTA[C/T]CCGCTGCACTACCTC	124930
rs772043200	in-del	-/CTC	0.000422495	0.0145282	intron-variant	ANKRD13B	GRCh38.p7	17:29607724	GGGCTTTATCTTCCA[-/CTC]CTCCTCCTCCTCCAG	124930
rs772080651	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29601361	CTAGTAGCTGGGATT[A/G]CAGGAATCCCCCACC	124930
rs772085682	snp	A/G	3.36005e-05	0.00409867	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612692	CCCAGCGTTGTTCGA[A/G]GCCCCGCGCGGCTAC	124930
rs772097666	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610112	CAGGAGAATTGCTTG[A/T]ACCTGGGAGGCGGAG	124930
rs772238918	snp	A/G	1.83927e-05	0.00303249	intron-variant	ANKRD13B	GRCh38.p7	17:29607710	CTCCGACGTGACTGG[A/G]GCTTTATCTTCCACT	124930
rs772341401	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613945	CTCCTTCTGGCCGGT[C/T]CGCATTTCTGTTCAC	124930
rs772362264	snp	G/T	1.65201e-05	0.00287398	intron-variant	ANKRD13B	GRCh38.p7	17:29611660	TGAGTGTGTGCAGGG[G/T]TACCCGTAAGTGGAG	124930
rs772422619	in-del	-/CGA	1.65179e-05	0.00287379	cds-indel, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612459	GAACCTCAACGGCTG[-/CGA]CGACGAACCGGTGCC	124930
rs772449873	snp	A/G	1.66796e-05	0.00288782	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612305	ATTTCTCCTGAGCCC[A/G]TGGCGGGCCGACCGG	124930
rs772648264	snp	C/T			upstream-variant-2KB, intron-variant	GIT1, ANKRD13B	GRCh38.p7	17:29591578	GTCCAAACTTTGTTT[C/T]CCCCAGCCCCGTCAC	124930
rs772809740	snp	A/G	1.73222e-05	0.00294292	intron-variant	ANKRD13B	GRCh38.p7	17:29607949	CTATGGTTGGCTGAA[A/G]GGTCCTGCCCTGTGA	124930
rs773094846	snp	G/T	1.65556e-05	0.00287707	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608936	AGACACCACACTCCT[G/T]GGCTTTGACCACATG	124930
rs773127231	snp	C/G	0.000167161	0.00914071	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612619	TGGGAGGGGCGCGCC[C/G]GGCCGTGCCTGACCC	124930
rs773144437	snp	A/G	1.83913e-05	0.00303238	intron-variant	ANKRD13B	GRCh38.p7	17:29607711	TCCGACGTGACTGGG[A/G]CTTTATCTTCCACTC	124930
rs773182372	snp	C/G	2.87608e-05	0.00379204	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612700	TGTTCGAGGCCCCGC[C/G]CGGCTACAGCATGAT	124930
rs773226141	snp	A/C/G	0.000358643	0.0133865	intron-variant	ANKRD13B	GRCh38.p7	17:29610681	TTTCTTCATCTGTCC[A/C/G]CAGGTGTATGGGGCA	124930
rs773292289	snp	C/T	1.65179e-05	0.00287379	intron-variant	ANKRD13B	GRCh38.p7	17:29611661	GAGTGTGTGCAGGGG[C/T]ACCCGTAAGTGGAGG	124930
rs773382960	snp	C/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614715	TCCCTGATGCCAGGG[C/G]CACCAGACTGATTCT	124930
rs773499538	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600736	CCTTTCAGGGGGGCT[-/G]GGGGTCACCTGGCTT	124930
rs773523793	snp	C/T	4.96833e-05	0.00498389	synonymous-codon, missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611935	CACTGCAGAAGAATA[C/T]TTCAACCCCAACTTT	124930
rs773577688	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598830	TGCTGGGATTACAGA[C/T]GTGAGCCCCCCGGCA	124930
rs773640250	snp	A/G/T	3.3643e-05	0.00410129	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609228	GAGCCGGCTTACCGC[A/G/T]CCCGTCGTCACCACT	124930
rs773673917	snp	C/T	2.24929e-05	0.0033535	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612427	CTTCCACATCCTCAA[C/T]GCCCGCATCACCTTC	124930
rs773768962	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606919	GCCAGACGTGTTGGC[A/G]AATGTCTGTAATCCC	124930
rs773789637	snp	A/C	0.000152964	0.00874405	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613462	GTTCCGGAGCTACGA[A/C]GAGCAGCTGCGGCTG	124930
rs773800016	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595635	GTTTCTCTCTCCCAC[C/T]CCTCTGGCTGCCTCA	124930
rs773840728	snp	G/T	0.00427348	0.0460269	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612604	TCTCCCCGGGGTGGG[G/T]GGGAGGGGCGCGCCC	124930
rs773867681	in-del	-/C			intron-variant	ANKRD13B	GRCh38.p7	17:29597028	AGACCTGCCCCTGCA[-/C]CCCACGCTGGGCAGG	124930
rs773911634	snp	C/T	3.56424e-05	0.00422136	intron-variant	ANKRD13B	GRCh38.p7	17:29609456	CTGCCAGCCCAGCTG[C/T]ACTCTTGCCTACAGC	124930
rs773918842	in-del	-/TG			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614683	AGAACAAAGAGAAAC[-/TG]TTCCTCCCACCCCCT	124930
rs774030034	snp	A/G	3.31126e-05	0.00406881	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608210	GCCCAGGACTTCTAC[A/G]TGGAGATGAAATGGG	124930
rs774036741	snp	A/G	1.69605e-05	0.00291204	intron-variant	ANKRD13B	GRCh38.p7	17:29609315	CCTTGAGCCAGCCCG[A/G]TGGGGTGCCTGCCTC	124930
rs774173424	snp	C/G	4.08305e-05	0.00451814	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612482	CCGGTGCCATCGGTG[C/G]GAGGCAGCCCCAGCA	124930
rs774279914	snp	C/T			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594224	TTTTAGCTCTCAAAC[C/T]GGGCAGATCCTTGGA	124930
rs774302092	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604507	AGCCACCGTGCCTGG[C/G]CTTTGATGCTAATTT	124930
rs774415170	snp	C/G	0.000158818	0.00890977	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593660	CAGGAAGGGGCCCGA[C/G]GGCAAGTATCCGCTG	124930
rs774509592	snp	G/T	1.65086e-05	0.00287298	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612138	GCCAAGCTGTGGCTG[G/T]GTGAGGAGCATCCCC	124930
rs774586732	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607152	TTCACAAAATTATAG[A/G]ATTTGTACAAATTTT	124930
rs774594803	in-del	-/GGG	0.0020555	0.0319925	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593897	CGGGAAAGGGTGATC[-/GGG]CCCTCCGGCCGGGAC	124930
rs774708102	snp	C/T	0.000214339	0.0103501	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613391	CGCCAGCCTGCGCCC[C/T]CGGCGTCAGTGCCCA	124930
rs774748460	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601807	AAGTTTTTGTTTTTG[-/T]TTTTTTCCCCCAGCA	124930
rs774825448	snp	C/T	1.67083e-05	0.00289031	intron-variant	ANKRD13B	GRCh38.p7	17:29609071	GATCCCCCTGTGCTG[C/T]TCCGTGTCTGGCAGA	124930
rs775048975	snp	C/T	0.000142969	0.00845366	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612574	GGCCCCCCGCGAGAA[C/T]GCCTGCCCCTCGGCT	124930
rs775165390	snp	A/T	1.71452e-05	0.00292785	intron-variant	ANKRD13B	GRCh38.p7	17:29610785	ATGAGGCAGAGCTGG[A/T]TGGGGAGAGGTGTTG	124930
rs775197708	snp	A/G	3.5264e-05	0.0041989	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612470	GGCTGCGACGAACCG[A/G]TGCCATCGGTGCGAG	124930
rs775264532	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605429	AAACACACACACACA[C/G]ACACATACACACACA	124930
rs775327582	snp	C/T	1.7221e-05	0.00293432	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608088	TGGCGGGCATCCCCG[C/T]GCTCCTGGAGAAGCT	124930
rs775389455	snp	C/T	1.83169e-05	0.00302623	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613048	GGAGAACCCGCGGGG[C/T]CCTCGGCAGGGACCC	124930
rs775412007	in-del	-/CTC	0.000422495	0.0145282	intron-variant	ANKRD13B	GRCh38.p7	17:29607723	GGGCTTTATCTTCCA[-/CTC]CTCCTCCTCCTCCTC	124930
rs775434350	in-del	-/C	0.000116381	0.00762737	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612560	GCTCCACGAGTGAGG[-/C]CCCCCCGCGAGAACG	124930
rs775603462	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609697	ATTCCCATTTTACGC[A/G]TGTTTATTGAGTCCT	124930
rs775906755	snp	C/G	1.84903e-05	0.00304053	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612910	CTGGGAGGCGCTAAC[C/G]AACAGCAAGCCAGGC	124930
rs775947551	snp	A/G	1.74986e-05	0.00295787	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607821	ACCTTGAGTGTGCCC[A/G]TGTGCTCCTGGCGCA	124930
rs775966497	snp	C/T	1.65641e-05	0.00287781	missense, synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611975	AACCGTGATATGGGC[C/T]GCCCCATGGAACTGA	124930
rs775978778	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29601379	GGAATCCCCCACCAC[A/G]CCCAGCTAATTTTTG	124930
rs776021756	snp	G/T	3.31587e-05	0.00407164	intron-variant	ANKRD13B	GRCh38.p7	17:29612072	TGCTGGGAGGCCATG[G/T]CTTCCTGCAGTGTCC	124930
rs776053332	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607286	AACCTCACTCAGTGA[A/T]AATGTCAGTGATCTA	124930
rs776074565	snp	C/G/T	3.4499e-05	0.00415313	intron-variant	ANKRD13B	GRCh38.p7	17:29607966	GTCCTGCCCTGTGAC[C/G/T]TTGCCTCGCCCTCCC	124930
rs776123798	snp	C/G	1.74634e-05	0.0029549	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608080	GAAGCGGCTGGCGGG[C/G]ATCCCCGTGCTCCTG	124930
rs776199636	snp	A/G			synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612209	GGCCGTCAGCAATGC[A/G]CTTTTTGCCAAGCTC	124930
rs776342689	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29608479	ACCTGCCGCTCCTTG[A/T]TAGAAGGTAAGCTCT	124930
rs776421577	snp	A/G	2.10351e-05	0.00324301	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612742	GGGAGGCGGCGACCC[A/G]GGACGACGACGACGA	124930
rs776472363	snp	A/G	1.66646e-05	0.00288652	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612308	TCTCCTGAGCCCGTG[A/G]CGGGCCGACCGGGGT	124930
rs776536640	snp	G/T	1.65537e-05	0.0028769	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611953	CAACCCCAACTTTGA[G/T]CTGGGCAACCGTGAT	124930
rs776539325	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597530	GACTCCAGCTGAGGC[C/T]TGCTGGGATAAGGAA	124930
rs776591242	snp	C/T	3.42454e-05	0.00413782	intron-variant	ANKRD13B	GRCh38.p7	17:29610680	CTTTCTTCATCTGTC[C/T]CCAGGTGTATGGGGC	124930
rs776591754	snp	A/G	1.65605e-05	0.0028775	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608962	ACATGACCTGGCAGC[A/G]AGGGAACCGCAGCTT	124930
rs776667871	in-del	-/T	1.89317e-05	0.0030766	frameshift-variant, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612888	ACGCCTCCCCGCAGG[-/T]CACCATCTGGGAGGC	124930
rs776812471	snp	A/G	0.00111085	0.0235412	synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593708	CAACCGCCACCGCGA[A/G]CTGGAGAAGGAGGTC	124930
rs776870496	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600324	AAGGTGATCAGGTGG[C/G]AGGCTGGCCTGTTCA	124930
rs776979273	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29611166	CTGGGTACCAGATAC[C/G]GTGTCCGAGGTGAAA	124930
rs777025921	snp	A/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614358	GCTGGGGTAAGCACT[A/G]GACCCAAGTAGACTG	124930
rs777142500	snp	C/T	3.59202e-05	0.00423778	intron-variant	ANKRD13B	GRCh38.p7	17:29607734	TTCCACTCCTCCTCC[C/T]CCTCCAGGTGGACAT	124930
rs777200614	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604831	TACAGGCATGAGCCA[C/T]TGCACCCGGCCTGAG	124930
rs777225369	snp	A/G	3.866e-05	0.00439642	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612875	ACGGCTAACGCCCAC[A/G]CCTCCCCGCAGGTCA	124930
rs777278754	snp	G/T	1.68343e-05	0.00290118	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613002	GAATCCTCCGGAGAG[G/T]ATCCTGTCTCCCCTA	124930
rs777470420	snp	A/G	1.67304e-05	0.00289222	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610758	AACAGCACAAGGGCA[A/G]GGTCAAAGGTAATGA	124930
rs777630893	snp	C/T	1.6495e-05	0.0028718	synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612236	GCTCCGGGACTTCAT[C/T]ACCCTGCGTCTGCCT	124930
rs777665761	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600617	CAGCTTAATGAGGCT[A/G]GGAAGGGGACCAGGG	124930
rs777801979	snp	G/T	9.15457e-05	0.00676495	splice-donor-variant	ANKRD13B	GRCh38.p7	17:29607879	CAGCGGCTGGACAGG[G/T]GGGCAGCCCTGCTCA	124930
rs777819034	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602519	CTTGTCTCTTTCAGA[G/T]TCTGGTGACTGGGCC	124930
rs777891112	snp	A/G	1.73773e-05	0.0029476	intron-variant	ANKRD13B	GRCh38.p7	17:29609430	AGCTAAGGTGAGGCT[A/G]CAGCTCCCAGCTGCC	124930
rs777940371	snp	C/T	1.7513e-05	0.00295908	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607797	TGCACCTGGCCACCA[C/T]GCTGGGGCACCTTGA	124930
rs778030167	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591895	GCGGGAGAAAGGGGC[A/G]AGGCAGCCCGCTCCT	124930
rs778086530	snp	A/G	1.69335e-05	0.00290972	intron-variant	ANKRD13B	GRCh38.p7	17:29608800	CCTGAGCTGGTCCAG[A/G]CCGTGTAGGCCAGAC	124930
rs778201161	in-del	-/G	3.3413e-05	0.00408722	intron-variant	ANKRD13B	GRCh38.p7	17:29612034	CGGTGCTGGGAAGGT[-/G]GGGGGGCCGGGGCTC	124930
rs778211551	snp	C/T	1.68912e-05	0.00290608	intron-variant	ANKRD13B	GRCh38.p7	17:29609287	AGAGGTGGGTGGACA[C/T]GGCCTTGGTCACCCT	124930
rs778298359	snp	A/G	0.000103622	0.00719723	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612553	CAGCTCCAGCTCCAC[A/G]AGTGAGGCCCCCCGC	124930
rs778397406	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615248	GTGTCTGCAGAACTG[A/G]GGTGACGCCCATCTG	124930
rs778414162	snp	C/G	3.46434e-05	0.00416179	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612690	TCCCCAGCGTTGTTC[C/G]AGGCCCCGCGCGGCT	124930
rs778434852	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29612069	AGATGCTGGGAGGCC[A/G]TGGCTTCCTGCAGTG	124930
rs778494511	snp	C/T	0.0008992	0.0211847	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612659	GCCCCCAGCCTCCTG[C/T]CGCGGCTGCGAGATC	124930
rs778495030	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600007	TCAGCCTCCCGAGTA[G/T]CTGTGACTACAGGCG	124930
rs778501520	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29596975	CCTACGCAGCTTGAG[A/G]ATGCATCCTGCCTCC	124930
rs778581252	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602171	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	124930
rs778593525	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598265	AGAAATTCCAGGACA[A/G]GGCTATAAAAATTAT	124930
rs778665903	snp	C/T	1.9613e-05	0.00313147	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612848	CGCGGGGCCACGGGA[C/T]TCCGCGCCGCCACGG	124930
rs778837097	in-del	-/AACTGACCA	1.64732e-05	0.0028699	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612287	GGTGAGACCGCACGG[-/AACTGACCA]CCATTTCTCCTGAGC	124930
rs778864657	snp	A/C	1.73884e-05	0.00294854	missense, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611877	CCCATGTGGTACAGA[A/C]CCTGATCACTCAGAC	124930
rs779002980	snp	G/T	1.69493e-05	0.00291108	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612524	TCCCCAGGCAGCGAC[G/T]CCTCCAGCGTCAGCA	124930
rs779067211	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29594970	GCATCCAGCTCTGCA[C/T]GGCAGTCCCTGTAAA	124930
rs779130013	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595580	TGGGGTGGGGGGCAC[C/G]GGAGCCGCTGCAGGT	124930
rs779180945	snp	C/T	1.66818e-05	0.00288802	intron-variant	ANKRD13B	GRCh38.p7	17:29608150	ACGGGAGCCCTTGAG[C/T]CCTTCTCCAGTGCAG	124930
rs779530201	snp	C/T	1.70327e-05	0.00291823	intron-variant	ANKRD13B	GRCh38.p7	17:29609307	TTGGTCACCCTTGAG[C/T]CAGCCCGGTGGGGTG	124930
rs779543330	snp	A/G			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29599432	CCAGTGAGAGATGGG[A/G]GGGCAACAGCTGCAA	124930
rs779575404	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598574	TTTTTCATGAGACAG[C/T]GTCTCACTCTGTCAC	124930
rs779619884	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592005	AGAGTTTGCAAGCTT[C/T]TGCTGGCACCTCCCA	124930
rs779688720	snp	G/T	4.89189e-05	0.00494541	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593643	CCCGCCAACGCCTCC[G/T]CCAGGAAGGGGCCCG	124930
rs779813336	snp	A/G	1.66181e-05	0.00288249	intron-variant	ANKRD13B	GRCh38.p7	17:29609013	AGGCAGGCAGGAAGT[A/G]GGGCAGGGTGGGGAC	124930
rs779850469	snp	A/G			missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613358	CCCACCCCCAGGAGC[A/G]CCCCGCCCACGCCGC	124930
rs779925784	snp	C/T	1.85005e-05	0.00304137	intron-variant	ANKRD13B	GRCh38.p7	17:29607701	GAGGGCTGCCTCCGA[C/T]GTGACTGGGGCTTTA	124930
rs780118283	snp	G/T	9.54991e-05	0.00690945	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612378	GGGCTGAGTGGTGGC[G/T]CCTAAAGGTTTCCTC	124930
rs780121647	snp	A/G	6.78564e-05	0.0058244	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613551	AGGAGGAGCTGGAGC[A/G]CATCCTGAGGCTCTC	124930
rs780231350	snp	A/G	2.92796e-05	0.00382609	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612979	GTCAGTGCCCGCTGG[A/G]CCGGAGAGAATCCTC	124930
rs780285555	snp	C/G	8.34425e-05	0.00645866	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610750	TCTTTCAGAACAGCA[C/G]AAGGGCAAGGTCAAA	124930
rs780321432	snp	A/G	1.69083e-05	0.00290755	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609171	TGGGCAGGACCGGGA[A/G]CTGCTGCTGGCTGCT	124930
rs780411568	snp	A/G			missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609187	CTGCTGCTGGCTGCT[A/G]CTCAGCCCACTGAGG	124930
rs780417079	snp	A/G	5.46991e-05	0.00522939	intron-variant	ANKRD13B	GRCh38.p7	17:29610660	ACCAGAACTGCTTAT[A/G]AGCCCTTTCTTCATC	124930
rs780418973	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610406	GTCTCCTTATAGAGA[C/T]TGTAAGTCTCAGGAG	124930
rs780488046	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29596367	CGGTGCCCTGCTTGC[C/T]GCTATGCATGTTCTC	124930
rs780506648	snp	A/C	3.07026e-05	0.00391796	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613522	GGAGAGGCGGCGGCG[A/C]GCGCGCCAGGAGGAG	124930
rs780520124	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592328	CTGACATCACAGTCC[C/T]CTCCCTCCAGGGACT	124930
rs780567196	snp	A/G	3.55259e-05	0.00421446	intron-variant	ANKRD13B	GRCh38.p7	17:29607925	CGGGGCCTCCCCAGC[A/G]TCATAGACCTATGGT	124930
rs780580404	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595080	CTCCGAGTTTCTCCT[C/G]AGACTGAACTCCTCA	124930
rs780636255	snp	C/T	0.00010125	0.00711442	intron-variant	ANKRD13B	GRCh38.p7	17:29610771	CAAGGTCAAAGGTAA[C/T]GAGGCAGAGCTGGAT	124930
rs780687451	snp	C/G	1.65198e-05	0.00287395	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611588	TTGTAGGCTGTAAGA[C/G]ACCTTTGCAGTCCTT	124930
rs780761537	snp	G/T	1.67545e-05	0.0028943	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608060	CGGGACTACCAGCGG[G/T]TGGTGAAGCGGCTGG	124930
rs780812444	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602071	GGTATTAGTTTCCAC[A/G]ACAAATTACTACAAA	124930
rs780829716	snp	A/C/G	3.35262e-05	0.00409417	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609099	AGACACAAGCGCCGT[A/C/G]GTCATGGAGATTGAC	124930
rs780837053	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29608766	CTGTTCCTGGCCACA[C/T]GGATCCCAAACCCCA	124930
rs780881722	snp	C/T	1.65767e-05	0.00287891	intron-variant	ANKRD13B	GRCh38.p7	17:29608177	GCAGACTTAGCCTCT[C/T]TCCCCTTCGTCCTCC	124930
rs780912450	snp	A/G	1.82347e-05	0.00301944	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612362	GAGGCTGAGGTGTGA[A/G]GGGCTGAGTGGTGGC	124930
rs781086963	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606260	CTCTCGAAATATATT[C/T]AAATACTTATGCTTA	124930
rs781233089	snp	C/T	7.57146e-05	0.00615236	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613028	CCCTAAGCCAGGACA[C/T]AGCCGGAGAACCCGC	124930
rs781238187	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595818	TCTCCTTCCCTCAGG[C/T]GTGCCAAAAAGAGGA	124930
rs781293009	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29599499	GAGGCAGAGCCTACA[A/G]GTTTTTCTGATGGGT	124930
rs781399101	snp	C/T	1.79603e-05	0.00299663	intron-variant	ANKRD13B	GRCh38.p7	17:29607906	CTCACCCCAGCCCCA[C/T]AGCCGGGGCCTCCCC	124930
rs781448930	snp	C/T	1.77341e-05	0.00297771	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607862	GTGGGCAGGGAGAAT[C/T]GCAGCGGCTGGACAG	124930
rs781463622	snp	A/G	1.65034e-05	0.00287253	synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612248	CATCACCCTGCGTCT[A/G]CCTCCTGGCTTCCCA	124930
rs781518441	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604866	ATTTTTAATCTGTTA[-/G]GGTGGGTCTAGGTGA	124930
rs781575748	snp	A/C	1.7221e-05	0.00293432	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612665	AGCCTCCTGCCGCGG[A/C]TGCGAGATCTCCCCA	124930
rs781592718	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606388	ACATATCAAAACCCC[A/G]TCTCTACTAAAATAC	124930
rs781600399	in-del	-/GA	1.65436e-05	0.00287602	intron-variant	ANKRD13B	GRCh38.p7	17:29611558	GTTGCGGTGTCCTCT[-/GA]GATGCCACATTTCTT	124930
rs781644030	in-del	-/TAATG			intron-variant	ANKRD13B	GRCh38.p7	17:29607286	AACCTCACTCAGTGA[-/TAATG]TCAGTGATCTAAATT	124930
rs781697868	snp	C/T	1.76309e-05	0.00296903	intron-variant	ANKRD13B	GRCh38.p7	17:29609445	GCAGCTCCCAGCTGC[C/T]AGCCCAGCTGCACTC	124930
rs796128391	snp	A/C			missense, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611885	GTACAGACCCTGATC[A/C]CTCAGACTCTGAGCC	124930
rs796494537	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29603868	CTGATTATAGGTTAT[A/G]TTTTCTTTCTTTTTT	124930

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