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

ANKRD13D

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1574103	snp	A/G	0.00844059	0.0644131	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290128	GTTTCCCAGAGACAC[A/G]GCCAGCTCCAGTGGG	338692
rs2004225	snp	A/T	0.209693	0.246729	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291228	CTGGGACCACAGGTG[A/T]GTGCCACCACTCCCA	338692
rs2051458	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291116	taatcccagcgcttt[C/T]tgaggccaaagtggg	338692
rs2298815	snp	A/G	0.108213	0.205904	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301388	GGTACCTGATGCGGC[A/G]ACAGCAGAGCTGGGG	338692
rs3802744	snp	A/G	0.0209421	0.100162	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299401	GGTTCAGACCCTGCC[A/G]CCTCCTCCATTTTGG	338692
rs3802745	snp	G/T	0.177182	0.23916	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299407	GACCCTGCCACCTCC[G/T]CCATTTTGGGGAGCA	338692
rs4244821	snp	C/T	0.188631	0.242351	intron-variant	ANKRD13D	GRCh38.p7	11:67297666	GAGTAGCTGGGACTA[C/T]AGGCGCCTGCCACCA	338692
rs4930192	snp	C/T	0.32885	0.23724	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302546	CCGCCATCCACAGTG[C/T]CTCTCCACAGCGCCC	338692
rs5792410	in-del	-/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290066	TGCTGGGGGAGACGG[-/G]ACACTCACAAAGGGC	338692
rs7104898	snp	A/G	0	0	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287707	GAAAAGAGGCCAGAC[A/G]GGAAGAACGTGGTCC	338692
rs10896166	snp	C/T	0.180064	0.240019	intron-variant	ANKRD13D	GRCh38.p7	11:67292980	ATCCAAGTTGTAGCA[C/T]GTAACTATTTCTTTC	338692
rs10896167	snp	C/T	0.454182	0.144256	intron-variant	ANKRD13D	GRCh38.p7	11:67298418	AGTGTTCCGTGTGCG[C/T]GTGAGAAGCGTGTGT	338692
rs11227758	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67289633	GGAGCCCCCCCCCCC[C/G]CCCCGCCCGCTCAGC	338692
rs11227759	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291809	TGCGGCTTGGGAGGA[C/T]GGTGCTGCCTTTTCT	338692
rs11227760	snp	A/G	0.01739	0.091611	intron-variant	ANKRD13D	GRCh38.p7	11:67298387	TTTCTTAATGGCCTA[A/G]TGTATGGCCTTGAAG	338692
rs11227761	snp	A/T	0.0569829	0.158885	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302952	TTTGCGCAAGTCACT[A/T]CCGCCTGCGTAGCTG	338692
rs11601700	snp	A/C	0.454182	0.144256	intron-variant	ANKRD13D	GRCh38.p7	11:67297031	ttaattttctctatt[A/C]tttttctattctcta	338692
rs11826864	snp	A/G	0.444444	0.157135	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302667	ACCCTCCGCCCCTCA[A/G]GGCTGAAAGGAGCTG	338692
rs12285051	snp	C/T	0.139564	0.224285	intron-variant	ANKRD13D	GRCh38.p7	11:67295213	acgaggtcaggagat[C/T]gagaccatcctggct	338692
rs12285097	snp	C/T	0.243061	0.249904	intron-variant	ANKRD13D	GRCh38.p7	11:67295289	aggcttggtggcggg[C/T]gcctgtaatcccagc	338692
rs12291831	snp	C/T	0.084364	0.187256	intron-variant	ANKRD13D	GRCh38.p7	11:67294908	taaaattacaattga[C/T]ttctgtatgttgacc	338692
rs34404014	snp	A/G	0.000486168	0.0155836	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299604	TCAGGACAAGTCGAG[A/G]AGCAAAGGTAAACCC	338692
rs34979469	in-del	-/T	0	0	intron-variant	ANKRD13D	GRCh38.p7	11:67297527	TCATAAGTTTTTTGG[-/T]TTTTTTTTTTTTTTC	338692
rs35159418	in-del	-/AC			intron-variant	ANKRD13D	GRCh38.p7	11:67298807	AAGGATGTTTTTAAA[-/AC]CCCAGCCCCGACACT	338692
rs35285998	in-del	-/C			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287327	GCAATGGCCTTTGAG[-/C]CCAGGCCTCCAGCAT	338692
rs35600142	in-del	-/G			frameshift-variant, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290421	GCTGGCGGGCATTCC[-/G]GGAACTGCTCAACAA	338692
rs35676170	in-del	-/C			intron-variant	ANKRD13D	GRCh38.p7	11:67295734	AGCAAGACTCCATCT[-/C]AAAACAGTAAATAAA	338692
rs35848734	in-del	-/GT/GTGT	0.433236	0.170072	intron-variant	ANKRD13D	GRCh38.p7	11:67296338	GCCATTTGGGCCTGA[-/GT/GTGT]GTGTGTGTGTGTGTG	338692
rs35965170	snp	G/T	0.0515216	0.152008	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292028	AGTGGACCATGACCG[G/T]CAGGTGGTGCATGTG	338692
rs35992096	in-del	-/C			frameshift-variant, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290373	GGTGCAGCTGGTGCT[-/C]CCAGTATCGGGACTA	338692
rs55733135	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293830	TCCCTTCACCCATTT[A/T]AAAAATTGGGTCATC	338692
rs56309751	in-del	-/GT/GTGT	0.5	0	intron-variant	ANKRD13D	GRCh38.p7	11:67296366	TGTGTGTGTGTGTGT[-/GT/GTGT]ATGTGTGTATAGTTT	338692
rs57589444	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67294636	ACCTCCACCTCCTGG[G/T]TTCAAGCAGTTCTCC	338692
rs58530946	snp	C/T	0.148661	0.22854	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288011	GAGCTGTGTTCAAGA[C/T]GGCAGAAATCAGGAG	338692
rs60229295	snp	C/T	0.177182	0.23916	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300885	GCAGGGCACTCCAGG[C/T]CAGGCAGAAGGTGGG	338692
rs61180657	snp	C/T	0.0733688	0.176922	intron-variant	ANKRD13D	GRCh38.p7	11:67298222	GTCCACCACCGTGCC[C/T]GGCTAATTTTTTGTA	338692
rs61300057	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67294381	TAGTACCATGTTAAC[A/T]ATGTTAAGTCTTCTA	338692
rs61740832	snp	C/T	0.0100107	0.0700367	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301059	GGTGACCCCCATCAT[C/T]GACCTAATGGCCATC	338692
rs61763974	snp	A/G	0.00356505	0.0420692	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287597	GTGAGAGCTGGCTCT[A/G]AAGTGATTGCCTGGT	338692
rs61763975	snp	C/G	0.00716837	0.0594373	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287904	CAATGGGAACGGACA[C/G]TCTCTCTCCCAGGGA	338692
rs61763977	snp	C/T	0.0228947	0.104514	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288215	CATAGCGTGGGGTGG[C/T]AAAGTGACCCCAGAT	338692
rs61763978	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288254	CGCCATGTGACTACA[A/G]GGAGAAGGCAGGGTA	338692
rs61763979	snp	C/T	0.0123036	0.0774623	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288413	GCCTTGGCCACCTAG[C/T]AAAACCAGGGCCCCA	338692
rs61763980	snp	A/G	0.00353981	0.0419211	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288554	CCTCTCCTGACGCTG[A/G]CAGCCAACCGCAGCC	338692
rs61763981	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288636	GTCCTCCGCCGGGAC[A/G]GCTCTGCCGCTGCCT	338692
rs61891565	snp	A/G	0.0379877	0.132479	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290643	ACGTGGGAGAGACTG[A/G]ACCCTTTGGAAGAGA	338692
rs61891566	snp	A/T	0.177182	0.23916	intron-variant	ANKRD13D	GRCh38.p7	11:67295209	GATCACGAGGTCAGG[A/T]GATCGAGACCATCCT	338692
rs71457771	snp	G/T	0.5	0	intron-variant	ANKRD13D	GRCh38.p7	11:67298489	GTCCAGCTGTAGTGT[G/T]GTTCTTATCTTCTGG	338692
rs71462369	snp	C/G	0	0	intron-variant	ANKRD13D	GRCh38.p7	11:67289632	TGGAGCCCCCCCCCC[C/G]CCCCGCCCGCTCAGC	338692
rs72930762	snp	G/T	0.0182019	0.0936463	intron-variant	ANKRD13D	GRCh38.p7	11:67292622	GTCAGTGGAAACACT[G/T]AAAAAAAAAAACAAA	338692
rs74475892	snp	C/T	0.00914312	0.0669923	intron-variant	ANKRD13D	GRCh38.p7	11:67298731	GTTTCCTAGAGTGTG[C/T]CAAAGCTCATCCCAG	338692
rs74736063	snp	A/C/G	0.00954224	0.0684493	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302694	GCTGGCGAGAGTCAC[A/C/G]TGTCCTTACCAAGCA	338692
rs74885508	snp	C/G	0.045891	0.144359	intron-variant	ANKRD13D	GRCh38.p7	11:67299933	GGCGGGGGGCCGAGC[C/G]TGGGCGGGAGGGCAC	338692
rs75299026	snp	G/T	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301961	TATCTGCCACCAAAG[G/T]TGGTGTGAGGGGTGG	338692
rs76001762	snp	C/T	0.5	0	intron-variant, synonymous-codon	ANKRD13D	GRCh38.p7	11:67300836	GGCCAGGACACCAGC[C/T]CCCGGGGGAGGCGGG	338692
rs76335959	snp	A/G	0.0115144	0.0749975	intron-variant	ANKRD13D	GRCh38.p7	11:67292931	TGCCTTTTGTGTCTG[A/G]CTTCTTTCACTTAGT	338692
rs76353068	snp	A/G	0.0479149	0.147179	intron-variant	ANKRD13D	GRCh38.p7	11:67294110	TCTGTCTTTATGCCA[A/G]TATTATACTGTCTTA	338692
rs76744563	snp	A/G/T	0.0418186	0.138422	intron-variant	ANKRD13D	GRCh38.p7	11:67296470	TAGTTTTGGTAGTTT[A/G/T]TGTCTCACTAGGAAT	338692
rs76764674	snp	A/T	0.0275645	0.114116	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291027	CCCTCTCCAGGGCAG[A/T]GTGGTTGGGCGTAGC	338692
rs76948867	snp	C/T	0.00703159	0.0588757	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301101	CTTTGCCAAGCTGCG[C/T]GACTTCATCACTCTG	338692
rs77616840	snp	C/T	0.0174175	0.0916809	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300375	TTCTATTGAATTTCA[C/T]GAGTACCTGCTGGGG	338692
rs77908999	snp	A/T	0.0372196	0.131242	intron-variant	ANKRD13D	GRCh38.p7	11:67298859	GCTAATTCCTCAGTG[A/T]CTTCTAGTCCCAAGT	338692
rs77913150	snp	A/G	0.00755907	0.0610114	intron-variant, synonymous-codon	ANKRD13D	GRCh38.p7	11:67300869	GCGGCATCTGAGCAG[A/G]GCAGGGCACTCCAGG	338692
rs77994298	snp	A/C	0.5	0	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300835	TGGCCAGGACACCAG[A/C]TCCCGGGGGAGGCGG	338692
rs78472376	snp	A/C	0.00914312	0.0669923	intron-variant	ANKRD13D	GRCh38.p7	11:67296086	ACTTGGTTGTGGTGT[A/C]TAATTCTTTTCATAT	338692
rs78657670	snp	A/G	0.0170251	0.090679	intron-variant	ANKRD13D	GRCh38.p7	11:67298903	TCCCCCCCTGTCCAG[A/G]CACCCTCTTCAGGGG	338692
rs78743307	snp	A/G	0.123452	0.215605	intron-variant	ANKRD13D	GRCh38.p7	11:67293229	ATTGTTTAATTGACT[A/G]TTTACCAAACGAGCT	338692
rs78822964	snp	C/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292172	CACTCGTAATGTGGC[C/G]TTTGAGAGGTCGGTC	338692
rs78926654	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296367	TGTGTGTGTGTGTGT[A/G]TGTGTGTATAGTTTT	338692
rs78983123	snp	A/C/G	1.65217e-05	0.00287412	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300081	TCAGCCTGGAGTCAC[A/C/G]GAACATTGGCCGCCC	338692
rs79176628	snp	A/T	0.5	0	intron-variant	ANKRD13D	GRCh38.p7	11:67295995	GATATGATCATGTGA[A/T]TTTTTAAAAAATTCT	338692
rs79226049	snp	A/G	0.0134861	0.0810011	intron-variant	ANKRD13D	GRCh38.p7	11:67292351	CTCACTCAGACTGCC[A/G]GGGTGGTTGGGCTCC	338692
rs79852510	snp	G/T	0.0418186	0.138422	intron-variant	ANKRD13D	GRCh38.p7	11:67297916	GAGACGTTGGCTATT[G/T]AGGAGTGTGTTGTTT	338692
rs80130094	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296993	TTTTGTTGATGTTTT[C/T]GAAGAGCCAGTTTTT	338692
rs111239786	snp	C/T	0.00392295	0.0441144	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299998	ACCCACGCAGGCCCC[C/T]GTGCAGCAGGCAGCC	338692
rs111345048	snp	C/G/T	0.00221253	0.0331869	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290064	GCCCTTTGTGAGTGT[C/G/T]CCGTCTCCCCCAGCA	338692
rs111349378	snp	G/T	0.176861	0.239062	intron-variant	ANKRD13D	GRCh38.p7	11:67295374	GTGAGCCAAAATCAC[G/T]CCACTTCACTCCAGC	338692
rs111687572	snp	A/G	0.5	0	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292034	CCATGACCGGCAGGT[A/G]GTGCATGTGGAGACA	338692
rs111935356	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67289638	CCCCCCCCCCCCCCC[C/G]CCCGCTCAGCTCCGC	338692
rs112095274	snp	C/T	0.00143431	0.0267413	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299061	GGTCTGTTTCAGGAA[C/T]AAATGTGGTATCTGG	338692
rs112286896	snp	C/G	0.5	0	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300129	AAGTACAGAGGTGAG[C/G]TCTGAGAGCTGGCTG	338692
rs112580474	snp	A/G	0.5	0	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288041	GAGGCTGGAACCAAG[A/G]AAGTCCTGTCGGGGT	338692
rs112865164	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302475	TGGAAATAAAGAGAC[C/T]GTCGCAGCAGGGCTG	338692
rs112895629	snp	A/C	0.140919	0.224948	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289169	AGACCCAAGGCCGGG[A/C]ATCTCCTCGGGCGCT	338692
rs112906755	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291593	CCAGTGACCCCTGTG[C/T]ACCCTGCAGTGCCCC	338692
rs113207481	snp	A/G	0.5	0	intron-variant	ANKRD13D	GRCh38.p7	11:67298223	TCCACCACCGTGCCC[A/G]GCTAATTTTTTGTAT	338692
rs113875221	snp	A/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290285	GCCAGGCCTGGGGTC[A/T]TCTGGAGGGCTCCCC	338692
rs114522764	snp	C/T	0.00597247	0.0543191	intron-variant	ANKRD13D	GRCh38.p7	11:67289791	CCGCATCCTTGCTGA[C/T]CCAAGCTGAGAACAA	338692
rs115593094	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288898	CCTGGGGTAGGAAGA[C/T]CGGGGCGAGCAAGGG	338692
rs115905247	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290518	ACTGTGCCAGGCCTG[A/G]CCTTGGAAAGGCACC	338692
rs117453503	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300472	AACAGAACAGTTACG[C/T]TCTTGCCTCGTGAGG	338692
rs138195189	snp	A/G	1.68783e-05	0.00290498	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301610	CTCCTGCAGTTCGCC[A/G]TCCAGCAGAGCCTGC	338692
rs138406797	snp	A/C	0.0111196	0.0737302	intron-variant	ANKRD13D	GRCh38.p7	11:67297286	GTGATAGCTCACTGC[A/C]ACCTCCGCCTCCCAG	338692
rs138461637	snp	C/T	0.000698556	0.0186759	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292025	GGAAGTGGACCATGA[C/T]CGGCAGGTGGTGCAT	338692
rs138486470	snp	A/T	0.00517822	0.0506191	intron-variant	ANKRD13D	GRCh38.p7	11:67293564	TGGAGTGCAGTGACA[A/T]GATCATGGCTCATTG	338692
rs138656438	snp	A/G	0.000682611	0.0184618	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301359	GAGCCCCTGAGCTCC[A/G]TGTGGGTGCCGGCCC	338692
rs138792309	snp	G/T	0.0372196	0.131242	intron-variant	ANKRD13D	GRCh38.p7	11:67294702	CCCACCACCACTCCT[G/T]GCTAATTTTTGCATT	338692
rs138807212	snp	C/T	0.00215163	0.032729	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301519	CGAGGTGGACCCCAC[C/T]GTGTTTGAAGTGCCC	338692
rs138888533	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292104	GCCATGCGGCCCAGC[A/G]AGGAGCATGTGGCCA	338692
rs138983611	in-del	-/GT			intron-variant	ANKRD13D	GRCh38.p7	11:67296339	GCCATTTGGGCCTGA[-/GT]GTGTGTGTGTGTGTG	338692
rs139186990	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302704	GTCACGTGTCCTTAC[C/T]AAGCAGGCGTCCTGT	338692
rs139229154	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298458	ATTGGGTAGAGTGTT[C/G]TAGCCTGCTTATGAA	338692
rs139513938	snp	C/T	0.00676609	0.0577691	intron-variant	ANKRD13D	GRCh38.p7	11:67295854	CCATTAAGTATGATA[C/T]TAGTTGTGAGTTTTT	338692
rs139609922	snp	C/T	1.6566e-05	0.00287797	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300041	CCCACAGCCATCTCC[C/T]CTGAGGAGTACTTCG	338692
rs140448867	snp	C/G	0.131381	0.220067	intron-variant	ANKRD13D	GRCh38.p7	11:67297258	TCCATCGCCCAGGCT[C/G]GAGTGCAGTGGTGTG	338692
rs140459437	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67295008	TTTTTTAACATATAA[A/G]ATTATGTTATCTGTA	338692
rs140521273	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291190	TGGTGAAAGCCGTCT[C/T]TACAAAAAGTACAAA	338692
rs140574351	snp	C/T	0.000146784	0.00856564	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299885	GCATTCCTCCCACAC[C/T]GGGGTGAGCCGGGGC	338692
rs140644794	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296148	GAGGATTTTGTGTCC[A/G]TATTCATAAGTGATA	338692
rs140647228	snp	A/C/G	0.000512456	0.0159991	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291695	AGTCTCCTGGGCTTC[A/C/G]AGCACATGACCTGGC	338692
rs140665288	snp	C/T	0.0178098	0.0926698	intron-variant	ANKRD13D	GRCh38.p7	11:67293130	AAGTTTTTGTGTAGA[C/T]GTATGTTTTAATTTC	338692
rs141025783	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287468	ATGCCAGGCTTAACC[C/T]ATCCCGGAGCCAGGT	338692
rs141097126	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67298813	TGTTTTTAAACCCAG[C/T]CCCGACACTATCATA	338692
rs141392969	snp	A/G	0.000200882	0.01002	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301563	TGCTGGGCATGGAGC[A/G]CAACGAGCCCCTCCG	338692
rs141465375	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13D	GRCh38.p7	11:67297046	ATTTTTCTATTCTCT[A/G]TTTCATTAACCTTTA	338692
rs141725111	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290690	GGCCTCCTGAAGAAT[A/G]CAGATTACCTGGAGC	338692
rs141739795	snp	A/C/G	8.45107e-05	0.00649993	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301171	CTGGGCACAGGCAGC[A/C/G]GGAGGACCTCAGGCA	338692
rs142068305	snp	G/T	0.0727599	0.17684	intron-variant	ANKRD13D	GRCh38.p7	11:67298284	TGCCAGGATGGTCTC[G/T]ATCTCCTGACCTCAT	338692
rs142136280	in-del	-/TTTTG			intron-variant	ANKRD13D	GRCh38.p7	11:67296607	TGAGTAATTTGAAGT[-/TTTTG]TTTTGTTTTGTTTTG	338692
rs142470779	snp	A/T	0.00398564	0.0444627	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300354	TGGTGCCACCCATGT[A/T]TGGTTTTCTATTGAA	338692
rs142499976	snp	A/G	0.0162398	0.0886349	intron-variant	ANKRD13D	GRCh38.p7	11:67295290	GGCTTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	338692
rs142732558	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293914	TTTGAGCCATTTTAA[A/G]TTAATTTTTGTGTAT	338692
rs142790480	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297319	TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCTGAG	338692
rs143234444	snp	A/G	0.00358779	0.0422022	intron-variant	ANKRD13D	GRCh38.p7	11:67297069	AACCTTTACTGTAAT[A/G]TTTATTATTTCTTTC	338692
rs143336561	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292736	TTCAGAGATTTGTAC[A/C]TCACCACAGTCAATT	338692
rs143357768	snp	A/T	1.65119e-05	0.00287327	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291616	AGTGCCCCTTGTGTC[A/T]AAGATGTGCCCAAGC	338692
rs143578575	in-del	-/TGTG			intron-variant	ANKRD13D	GRCh38.p7	11:67296346	GGCCTGAGTGTGTGT[-/TGTG]GTGTGTGTGTGTGTG	338692
rs143743620	snp	C/T	1.66796e-05	0.00288782	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301318	TCAATGCCCGCATCA[C/T]CTTCAGCAACCTGTG	338692
rs143781397	in-del	-/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292516	ATTGGTGCGGCTGTG[-/T]TTGGGGGCAGAATCC	338692
rs144038054	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294763	CCAGGCTGGTCTCCA[A/G]CTCCTGACCTTGCTG	338692
rs144144755	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67297905	ATTTATTATTTGAGA[C/T]GTTGGCTATTTAGGA	338692
rs144238691	snp	A/G	5.50232e-05	0.00524486	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299886	CATTCCTCCCACACC[A/G]GGGTGAGCCGGGGCT	338692
rs144267578	snp	C/G	0.0140233	0.0825529	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290254	CCTGAGGCTGGCAGG[C/G]GGGGGGCAGTGAGCA	338692
rs144383283	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67298490	TCCAGCTGTAGTGTT[A/G]TTCTTATCTTCTGGT	338692
rs144422673	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67296391	TAGTTTTTTGTTGTT[A/G]TATTTACCAATCAGT	338692
rs144568493	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290895	CTGAGACCCAGTGGA[A/G]ACAAAGGCTCCCCCA	338692
rs144569146	snp	A/G	0.000350769	0.0132386	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292140	CTCACCTCTCCTATC[A/G]TCTCCACCCACCTGG	338692
rs144969259	snp	C/T	0.000149909	0.00865632	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292088	CGAAACACTGCTGGC[C/T]GCCATGCGGCCCAGC	338692
rs145025950	snp	C/T	0.000150267	0.00866665	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301516	GTGCGAGGTGGACCC[C/T]ACCGTGTTTGAAGTG	338692
rs145045712	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292318	GCTCAGGGGCAGGTG[G/T]GTTGCTGCAGCCCGT	338692
rs145635841	snp	G/T	0.0271762	0.113356	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288925	AGGGGATCCGCGGGG[G/T]AAACGCAGGCATCAC	338692
rs145855005	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293286	CATGTGAGGGTTCCA[A/G]TTTCTCCACATCCTC	338692
rs145871942	snp	C/T	0.00438332	0.0466095	intron-variant	ANKRD13D	GRCh38.p7	11:67299724	AGGCCTCCCCATTCC[C/T]GTCTGACCCCTCTTC	338692
rs145898443	in-del	-/C			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302651	AGGAGACCACCCCCC[-/C]ACCCTCCGCCCCTCA	338692
rs146192337	snp	A/G	0.000669959	0.0182902	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301645	AGCGGGCACTGAGGC[A/G]GAGCAGGTGGGACTT	338692
rs146203431	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298306	TGACCTCATGATCCA[A/C]CCCCCTTGGCTTCCC	338692
rs146628705	snp	G/T	0.0792508	0.182605	intron-variant	ANKRD13D	GRCh38.p7	11:67296660	TTTGAGACAGAGTCT[G/T]ACTCTGTCACCCAGG	338692
rs146945143	snp	A/T	0.00279162	0.0372561	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287300	TACTCAGGGCTGAAT[A/T]CAAGAGTCAGGGGCA	338692
rs146982557	snp	C/G	0.000798403	0.0199641	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300886	CAGGGCACTCCAGGC[C/G]AGGCAGAAGGTGGGT	338692
rs147412452	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67297414	TGCACAGGCTGGTCT[C/T]GAACTCCTGTGCTCA	338692
rs147851366	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290905	GTGGAAACAAAGGCT[C/T]CCCCAGGGCTCTGCA	338692
rs148039822	in-del	-/TGTG			intron-variant	ANKRD13D	GRCh38.p7	11:67296356	TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTATGTG	338692
rs148311601	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297072	CTTTACTGTAATATT[C/T]ATTATTTCTTTCTGT	338692
rs148457831	snp	C/T	1.67913e-05	0.00289748	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292149	CCTATCGTCTCCACC[C/T]ACCTGGACACTCGTA	338692
rs148607495	in-del	-/TTTGTC	0.0410537	0.137264	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300320	ACAGAAAACCGGTAG[-/TTTGTC]TTTGATGAATGGATG	338692
rs148920209	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67299751	CTTCCCCCAGACAGT[A/G]GGCTCCAGGGGTGGA	338692
rs148986056	snp	C/T	0.000115935	0.00761277	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301080	AATGGCCATCAGCAA[C/T]GCTCACTTTGCCAAG	338692
rs149068274	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67292661	ATTGAGATATAATCT[C/T]ATATACCATATAAGA	338692
rs149238471	snp	A/C/T	0.00015204	0.00871771	upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301606	TGACCTCCTGCAGTT[A/C/T]GCCATCCAGCAGAGC	338692
rs149376071	snp	A/G	0.000664871	0.0182207	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292109	GCGGCCCAGCGAGGA[A/G]CATGTGGCCAGTCGC	338692
rs149388826	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294744	AGGATTTCACCATGT[C/T]GGACCAGGCTGGTCT	338692
rs149514380	snp	C/G	6.78196e-05	0.00582282	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301624	CATCCAGCAGAGCCT[C/G]CTTGAAGCGGGCACT	338692
rs149548732	snp	A/G	0.0134861	0.0810011	intron-variant	ANKRD13D	GRCh38.p7	11:67297777	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	338692
rs149680069	snp	A/T	0.0170251	0.090679	intron-variant	ANKRD13D	GRCh38.p7	11:67296001	ATCATGTGATTTTTT[A/T]AAAAATTCTATTGAT	338692
rs149839997	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67298957	GGGGCCCTGAGAGTT[A/G]GGCACCCCGGGCAGG	338692
rs150199846	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67294222	GTATTTTGGGACCCT[C/T]GCATTTTATATGAAT	338692
rs150418624	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13D	GRCh38.p7	11:67297266	CCAGGCTGGAGTGCA[A/G]TGGTGTGATAGCTCA	338692
rs150429952	snp	A/G	3.34891e-05	0.00409187	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301566	TGGGCATGGAGCGCA[A/G]CGAGCCCCTCCGGGA	338692
rs150486121	snp	A/G	1.65712e-05	0.00287843	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291720	CCTGGCAGCGGGGCC[A/G]GAGGAGCTTCATCTT	338692
rs150572357	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290780	GCACCCTTCTGGAAG[C/G]ACACGGAGGGGCCTG	338692
rs150594878	snp	A/G	7.31088e-05	0.00604558	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299872	GGATGGCGCAGCAGC[A/G]TTCCTCCCACACCGG	338692
rs150960363	snp	G/T	0.00318978	0.0398085	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287347	GCCTCCAGCATTGGT[G/T]TGGGAAGGAGGGAGG	338692
rs151299952	snp	A/G	0.000231134	0.0107477	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291637	GTGCCCAAGCGATGT[A/G]TACCGCGTGTGGAAG	338692
rs151312045	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67293110	CACTCTAAGTATTCA[C/T]GTGCAAGTTTTTGTG	338692
rs180690336	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13D	GRCh38.p7	11:67293485	ATTCAGATCCTTTAC[C/T]CATTTTTTATTTAAC	338692
rs181174249	snp	A/G	0.000329942	0.0128399	intron-variant	ANKRD13D	GRCh38.p7	11:67299780	GAGGTGGGCAGGGGC[A/G]ATGCGAGCATTGTGA	338692
rs181631867	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13D	GRCh38.p7	11:67298979	CCGGGCAGGCTGGCT[A/G]GAGGGGGCTTTGGAA	338692
rs181866480	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294026	TCTTGTCACCCTTGT[C/T]GAAAATCAGTTGACC	338692
rs181926332	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287898	GGGTGACAATGGGAA[C/T]GGACAGTCTCTCTCC	338692
rs182258235	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67297585	GGCTGGAGTGCAGTG[A/G]CACGATCTCGGCTTA	338692
rs182451583	snp	A/G	0.00438332	0.0466095	intron-variant	ANKRD13D	GRCh38.p7	11:67295427	ATCTCAAAAAAAAAG[A/G]GGGGTGGTTAGAGCA	338692
rs182751905	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67289797	CCTTGCTGACCCAAG[C/G]TGAGAACAAGAACTC	338692
rs183089787	snp	G/T	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67294545	TTTTGTTTTGTTTTT[G/T]TGTTTTTTTTTTTGA	338692
rs183188841	snp	A/G	0.000461095	0.0151768	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290103	AACAGGAGGACCCCC[A/G]CGGGCGGACCCCACT	338692
rs183378354	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291016	CACTTGGCCCACCCT[C/T]TCCAGGGCAGAGTGG	338692
rs183794538	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297484	ACAGGCGTGAGCCAC[C/T]GGGCCTGGCCTGGCC	338692
rs183831436	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67300548	CAAGCCTAGCGCTCT[C/G]CCCACCATCTCAGGA	338692
rs183935393	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302970	GCCTGCGTAGCTGGA[A/C]GCCCTGCCCTGCTCG	338692
rs183978405	snp	A/G	9.99617e-05	0.00706901	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300157	CTGGGGACTTGCCTC[A/G]GGACAAGGGCTCTTG	338692
rs183985561	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295905	TTAAGGTAATTCCTT[C/T]CCATTCCTCATTGTT	338692
rs184751377	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67292562	GGAACCTGACCCTTC[C/T]AGCAAGAGTTTCTCT	338692
rs184791435	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297232	TTTCTTTTTTTGACA[C/T]GGGGTCTCACTCCAT	338692
rs185439482	snp	A/G	0.000366555	0.013533	intron-variant	ANKRD13D	GRCh38.p7	11:67299785	GGGCAGGGGCGATGC[A/G]AGCATTGTGACCCCT	338692
rs185567432	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67297815	CAGGCGTGAGCCACC[A/G]TGCCCGGCCATAAGT	338692
rs186055488	snp	A/G/T	8.3106e-05	0.00644569	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299148	GGCTAGGGGTGGGGG[A/G/T]CTGGGGGTAGGAGAT	338692
rs186306958	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13D	GRCh38.p7	11:67294681	AAGTAGCTGGGATTA[C/T]AGGTGCCCACCACCA	338692
rs186308820	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293829	ATCCCTTCACCCATT[C/T]AAAAAATTGGGTCAT	338692
rs186770605	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67295516	GATCACTTGAGGTCA[A/G]GAGTTTGAGACTAAG	338692
rs186868833	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67297293	CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCAAG	338692
rs186894581	snp	A/G	0.00438332	0.0466095	intron-variant	ANKRD13D	GRCh38.p7	11:67294142	TCACTGTTGCTTTGC[A/G]ATAAGTTTTGAAATT	338692
rs186933117	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13D	GRCh38.p7	11:67290004	CACAGCGATTCCCAA[C/T]CCTGCTCGCCCTGGC	338692
rs187357192	snp	C/T	0.000100771	0.00709756	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301403	TGCCGCATCAGGTAC[C/T]CCAACGGGAGGAAGA	338692
rs187644391	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290662	CTTTGGAAGAGAAGC[C/T]TTGCCAGCTTTGGGC	338692
rs187722568	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291288	CCTGAGCCCAGGGAG[G/T]CAGAGGTTGCAGTGA	338692
rs188070724	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67297485	CAGGCGTGAGCCACC[A/G]GGCCTGGCCTGGCCT	338692
rs188248371	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293140	GTAGACGTATGTTTT[A/C]ATTTCTCTTTCATAT	338692
rs188430010	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67296385	TGTGTATAGTTTTTT[A/G]TTGTTATATTTACCA	338692
rs188878334	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300240	TCTCTCTGGACTCCA[C/T]TCCTGGAGGGCAGGA	338692
rs189387249	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287533	GACATGGAGTCCAGA[A/C]CTGCCATGCTCAGGG	338692
rs189483945	snp	G/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67293987	CCCCTTTGTTGAAAA[G/T]ACTATGTTTTTCCCA	338692
rs189707125	snp	A/T	3.31642e-05	0.00407198	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300130	AGTACAGAGGTGAGG[A/T]CTGAGAGCTGGCTGG	338692
rs189882985	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67295342	GAATGGTGTGAACCC[A/G]GGAGGCAGAGCTTGC	338692
rs189995219	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297891	TGATTTCTCTTTTGA[G/T]TTATTATTTGAGACG	338692
rs190419253	snp	C/G	0.00153509	0.027662	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299494	TGTGGGGAGCAGGCT[C/G]TGAGCCCCCAGCTCC	338692
rs190522530	snp	C/G	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67289713	GTCACCGGCCCCTCG[C/G]GCCTGAGCCTCTGGC	338692
rs191312842	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290768	ACTTGCTACTACGCA[C/T]CCTTCTGGAAGCACA	338692
rs191628952	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300470	GGAACAGAACAGTTA[C/T]GCTCTTGCCTCGTGA	338692
rs191652461	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67297351	AGCTGGGAACACAGG[C/T]GCCAGCTAATTTTTT	338692
rs191781573	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67294407	TTCTAATCCGTGAAC[A/G]TGGGATGTTTTTCCA	338692
rs191800510	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301879	GCCCTGGCTTGGCGG[A/G]GAGGGGGATAGCAGG	338692
rs192481208	snp	C/T	8.25689e-05	0.00642477	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291643	AAGCGATGTGTACCG[C/T]GTGTGGAAGCGGGGT	338692
rs192597182	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295785	AGTGGTTAGAGCAGA[A/C]ATCCTTGTATTCTTG	338692
rs192769717	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67292433	ACTTCTGACCTCATA[C/T]GTTTTCCCATTAAGA	338692
rs193057073	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297205	ATTACATTTATACTT[C/T]TAGGCATGTCTTTTC	338692
rs199554847	snp	A/G	0.000264489	0.0114967	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291569	GGGGTGGGGCCTTTG[A/G]AAAGACCCCCAGTGA	338692
rs199759076	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293239	TGACTGTTTACCAAA[C/T]GAGCTGTACTGGTTT	338692
rs200066974	in-del	-/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297961	TGTGAATTTCCAAAG[-/T]TTTTTTTTTCTGCTA	338692
rs200338165	snp	A/G	3.35003e-05	0.00409256	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301389	CCCAGCTCTGCTGTT[A/G]CCGCATCAGGTACCC	338692
rs200908072	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298365	CCGCGCCCGGACTTA[C/T]TGAGGTTTTCTTAAT	338692
rs200939455	in-del	-/TTTTTTTTTTTTTTT			intron-variant	ANKRD13D	GRCh38.p7	11:67298057	TTTATTGAGGTTTTC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTGAGAC	338692
rs200947046	snp	A/G	0.00199793	0.0315432	intron-variant	ANKRD13D	GRCh38.p7	11:67299896	ACACCGGGGTGAGCC[A/G]GGGCTGGGCCGAGAC	338692
rs201238208	snp	C/T	0.000552019	0.0166044	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301263	CCGCCAGGGCTCAGG[C/T]GTGGCTGTCTTCTCA	338692
rs201240270	snp	C/T	1.68525e-05	0.00290275	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301428	GGAAGAGGGAGCCTG[C/T]ACAGCTTTCTGGTCA	338692
rs201571514	snp	A/G	3.3e-05	0.00406189	intron-variant	ANKRD13D	GRCh38.p7	11:67299042	GTCTCACCAGCTCCT[A/G]TTTGGTCTGTTTCAG	338692
rs201756469	snp	A/G	3.31708e-05	0.00407238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291448	AGCAGCAGGCAGGGC[A/G]CTGACAAGCAGCTCT	338692
rs201807860	snp	C/T	1.69481e-05	0.00291098	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301294	CAGAGATTCCCCTTT[C/T]CCACGTGCTCAATGC	338692
rs201999693	snp	A/G	0.000155326	0.0088113	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292031	GGACCATGACCGGCA[A/G]GTGGTGCATGTGGAG	338692
rs267603134	snp	C/T			upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301499	CTAGGGAACCCTTTC[C/T]CGTGCGAGGTGGACC	338692
rs367623089	snp	A/G	3.36683e-05	0.00410281	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301301	TCCCCTTTTCCACGT[A/G]CTCAATGCCCGCATC	338692
rs367859818	in-del	-/TTAAG			intron-variant	ANKRD13D	GRCh38.p7	11:67293910	GGTCTTTGAGCCATT[-/TTAAG]TTAATTTTTGTGTAT	338692
rs367884623	snp	G/T	1.66618e-05	0.00288628	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292086	CCCGAAACACTGCTG[G/T]CCGCCATGCGGCCCA	338692
rs367905510	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13D	GRCh38.p7	11:67293227	TCATTGTTTAATTGA[C/T]TGTTTACCAAACGAG	338692
rs367926614	snp	C/T	0.000100756	0.00709702	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301582	CGAGCCCCTCCGGGA[C/T]GAGGACGATGACCTC	338692
rs368102605	snp	C/T	6.99962e-05	0.0059155	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291796	CCCTTGGGTTTCCTG[C/T]GGCTTGGGAGGACGG	338692
rs368498130	in-del	-/C			intron-variant	ANKRD13D	GRCh38.p7	11:67289622	GCCTCCGTCCTGGAG[-/C]CCCCCCCCCCCCCCC	338692
rs368501026	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298351	ACAGGCATGAGCCAC[C/T]GCGCCCGGACTTATT	338692
rs368504536	snp	C/T	1.68616e-05	0.00290353	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301449	TTTCTGGTCACCAAG[C/T]CCCGCGGGTTGAGCG	338692
rs368543003	snp	C/T	0.000111663	0.00747122	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290497	TGGCAGGGCACCACC[C/T]TGGTTACTGTGCCAG	338692
rs368733850	snp	A/G	0.000347537	0.0131775	intron-variant	ANKRD13D	GRCh38.p7	11:67300956	GAAGGGCCACCAGCC[A/G]TGCCTCACCCATGTC	338692
rs368781516	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67293769	GCGACCTGCCTACCT[G/T]GGCCTCCCACAGTGC	338692
rs369002025	snp	C/G			intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300787	CTCAGGAGCCCCAGC[C/G]TGGGCCCAGGGAGGA	338692
rs369072835	in-del	-/A			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291351	GACAGAGCAAGTCTC[-/A]AAAAAAAAAAAAAAA	338692
rs369106639	snp	A/G	0.000153988	0.00877327	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301615	GCAGTTCGCCATCCA[A/G]CAGAGCCTGCTTGAA	338692
rs369237025	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67294799	ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCACTAA	338692
rs369244938	snp	C/T	1.80536e-05	0.00300441	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301695	GCCTCTGCAGCCACA[C/T]GGCAGAAGTGACAGC	338692
rs369287312	snp	A/G	0.000114694	0.00757192	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291943	CTCTGCACTGCTGGC[A/G]CCCAGCACTGATTTG	338692
rs369386211	snp	C/T	0.00303336	0.0388263	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302343	ACTGAGCCATAGCCC[C/T]GGGAGGGCTGGCCAG	338692
rs369386492	snp	A/G	0.000157987	0.00888644	intron-variant	ANKRD13D	GRCh38.p7	11:67299655	CGGTCACACCGTGTG[A/G]TGGGGTCACCCTGGC	338692
rs369390716	snp	A/G			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288470	AAGGGCCGGAACTGA[A/G]CTGACGGAGGCCTGC	338692
rs369430278	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67299725	GGCCTCCCCATTCCC[A/G]TCTGACCCCTCTTCC	338692
rs369530442	snp	A/G	0.000588939	0.01715	intron-variant	ANKRD13D	GRCh38.p7	11:67299907	AGCCGGGGCTGGGCC[A/G]AGACAGGGCTGGCGG	338692
rs369588660	snp	C/G/T	8.27238e-05	0.00643085	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291478	TGGTTTCTCTTAGGC[C/G/T]CCCGATTTCTACGTT	338692
rs369646145	snp	C/T	9.77565e-05	0.00699061	intron-variant	ANKRD13D	GRCh38.p7	11:67299632	CCCAGGTGCGCCTGC[C/T]TGCTGCCCGGTCACA	338692
rs369648359	snp	A/C			intron-variant	ANKRD13D	GRCh38.p7	11:67295367	GCTTGCAGTGAGCCA[A/C]AATCACGCCACTTCA	338692
rs369774613	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300216	AGGGACCCACTCCCT[C/T]GGCTGGCTTCTCTCT	338692
rs369999370	snp	C/G/T	3.48938e-05	0.00417683	intron-variant	ANKRD13D	GRCh38.p7	11:67299976	TGATGGCTGAGTCCG[C/G/T]CCTGGGACCCACGCA	338692
rs370003122	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290738	TCGGTGGATTATGGC[C/T]TGAAACCCTGGAATA	338692
rs370090490	snp	A/G	0.000155988	0.00883004	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302299	GGAGGAGGACTTACA[A/G]CGGATCCTGCAGCTG	338692
rs370268991	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297635	GGTTCACGCCATTCT[C/T]CTGGCTCAGCCTCCC	338692
rs370340276	snp	C/T	0.000307953	0.0124049	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300156	GCTGGGGACTTGCCT[C/T]GGGACAAGGGCTCTT	338692
rs370346229	snp	C/T	0.00379898	0.0434173	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301249	GCACAGGTGGCTCTC[C/T]GCCAGGGCTCAGGCG	338692
rs370375085	snp	C/T	0.000247711	0.0111263	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291653	TACCGCGTGTGGAAG[C/T]GGGGTGAGAGCCTGC	338692
rs370552873	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290019	CCCTGCTCGCCCTGG[C/T]AGCCTCCCTGCCTTG	338692
rs370777430	snp	A/G	3.30409e-05	0.0040644	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291660	TGTGGAAGCGGGGTG[A/G]GAGCCTGCGAGTAGA	338692
rs370874560	snp	A/G	1.6517e-05	0.00287372	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291654	ACCGCGTGTGGAAGC[A/G]GGGTGAGAGCCTGCG	338692
rs370919136	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67300648	CATAAAAGTTTGGCA[A/G]CACGTGAGCTGGTGA	338692
rs370944826	snp	C/T	6.61485e-05	0.00575064	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300055	CCCTGAGGAGTACTT[C/T]GACCCCAACTTCAGC	338692
rs370950657	snp	A/G	8.8136e-05	0.00663779	intron-variant	ANKRD13D	GRCh38.p7	11:67292203	GGGTCCTGGCACACC[A/G]TGGGTGGGATGGGGA	338692
rs371023473	snp	C/T			upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302052	AAGCCGGTCCCCAGC[C/T]CCTCGGCTTCTGCCC	338692
rs371069737	snp	A/G	0.00143812	0.0267767	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290413	CACGCAGAGGCTGGC[A/G]GGCATTCCGGAACTG	338692
rs371167553	snp	C/T	3.31334e-05	0.00407009	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301071	CATCGACCTAATGGC[C/T]ATCAGCAACGCTCAC	338692
rs371176368	snp	C/T	1.65012e-05	0.00287234	intron-variant	ANKRD13D	GRCh38.p7	11:67299029	TGTGAGGGTGCAGGT[C/T]TCACCAGCTCCTGTT	338692
rs371187597	snp	C/G			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287697	AGGAAGAGATGAAAA[C/G]AGGCCAGACGGGAAG	338692
rs371190314	snp	A/G	6.67646e-05	0.00577736	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301314	GTGCTCAATGCCCGC[A/G]TCACCTTCAGCAACC	338692
rs371219970	snp	A/G	0.000199352	0.0099818	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299146	GAGGCTAGGGGTGGG[A/G]GGCTGGGGGTAGGAG	338692
rs371391783	snp	A/G	0.000153988	0.00877328	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301589	CTCCGGGACGAGGAC[A/G]ATGACCTCCTGCAGT	338692
rs371435656	snp	A/G	4.96339e-05	0.00498142	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299116	ACTGTTAGCGGCTAC[A/G]AGGCCAAGGCAGGAG	338692
rs371618840	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293938	TGTGTATAGTGGAAG[A/G]TTCTTTTGCATGTGA	338692
rs371734896	snp	C/T	0.000297929	0.0122015	intron-variant	ANKRD13D	GRCh38.p7	11:67299920	CCGAGACAGGGCTGG[C/T]GGGGGGCCGAGCCTG	338692
rs371782833	snp	A/G	5.05625e-05	0.00502779	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301453	TGGTCACCAAGCCCC[A/G]CGGGTTGAGCGTGGC	338692
rs371802130	snp	A/G	1.73966e-05	0.00294924	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292027	AAGTGGACCATGACC[A/G]GCAGGTGGTGCATGT	338692
rs372128375	snp	C/T			missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301084	GCCATCAGCAACGCT[C/T]ACTTTGCCAAGCTGC	338692
rs372310587	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298003	TTTCATTCCATTGTG[A/G]TTGGAAAACATACAT	338692
rs372376286	snp	C/G/T	0.000547411	0.0165366	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299495	GTGGGGAGCAGGCTC[C/G/T]GAGCCCCCAGCTCCC	338692
rs372393966	in-del	-/CA	0.00438332	0.0466095	intron-variant	ANKRD13D	GRCh38.p7	11:67292741	AGATTTGTACATCAC[-/CA]CAGTCAATTTTAGAA	338692
rs372406841	snp	A/G	1.85813e-05	0.003048	intron-variant	ANKRD13D	GRCh38.p7	11:67299926	CAGGGCTGGCGGGGG[A/G]CCGAGCCTGGGCGGG	338692
rs372860650	snp	C/T	0.00557542	0.0525036	intron-variant	ANKRD13D	GRCh38.p7	11:67298416	AGAGTGTTCCGTGTG[C/T]GCGTGAGAAGCGTGT	338692
rs373106878	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289022	CTCCGGCCCCGCCTT[C/T]CTCTTCCGGACCCGG	338692
rs373112645	in-del	-/TCTTTG			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300324	AAAACCGGTAGTTTG[-/TCTTTG]ATGAATGGATGGTGC	338692
rs373153272	snp	A/G	9.79096e-05	0.00699609	intron-variant	ANKRD13D	GRCh38.p7	11:67299641	GCCTGCCTGCTGCCC[A/G]GTCACACCGTGTGGT	338692
rs373342020	snp	A/G			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300425	AGGGCCCCCAGCGAC[A/G]TGGCCTGGGAGTGGA	338692
rs373358064	snp	C/G	1.70214e-05	0.00291726	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299994	TGGGACCCACGCAGG[C/G]CCCCGTGCAGCAGGC	338692
rs373465801	snp	G/T	1.84235e-05	0.00303503	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291982	CTGTCCACCCCTACC[G/T]GCCGGCAGAGGCAGG	338692
rs373466663	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293865	GATTATTGAGTCATA[C/G]GAGTTTTATAATTTT	338692
rs373530432	snp	A/C/G	3.31919e-05	0.0040737	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291436	CCTGCTGGAGCCAGC[A/C/G]GCAGGCAGGGCGCTG	338692
rs373537720	snp	A/C/T	0.000596209	0.0172565	upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302300	GAGGAGGACTTACAG[A/C/T]GGATCCTGCAGCTGT	338692
rs373538821	snp	C/T	1.90232e-05	0.00308403	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301720	GACAGCTGTGGGCTC[C/T]GGTGGCTGCAGGTGA	338692
rs373575344	snp	A/G/T	7.32633e-05	0.00605203	intron-variant	ANKRD13D	GRCh38.p7	11:67299792	GGCGATGCGAGCATT[A/G/T]TGACCCCTTACCAGC	338692
rs373582844	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301230	AGAGCTGCAGGGGCC[A/G]GAGGCACAGGTGGCT	338692
rs373727800	snp	C/T	5.17808e-05	0.005088	intron-variant	ANKRD13D	GRCh38.p7	11:67299984	GAGTCCGCCCTGGGA[C/T]CCACGCAGGCCCCCG	338692
rs373828270	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295396	CACTCCAGCCTGGGC[A/G]ACAGACCAAGACTCC	338692
rs373867818	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290943	ATGGCCAGGTTGAGG[C/T]TGGCCCTCCACCTCC	338692
rs373975192	snp	C/T	1.65299e-05	0.00287483	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300061	GGAGTACTTCGACCC[C/T]AACTTCAGCCTGGAG	338692
rs373993670	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299161	GGGCTGGGGGTAGGA[A/G]ATGAGGTCCAGGAAC	338692
rs373999660	snp	C/T	4.96331e-05	0.00498138	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291479	GGTTTCTCTTAGGCC[C/T]CCGATTTCTACGTTG	338692
rs374122779	snp	C/G			missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301302	CCCCTTTTCCACGTG[C/G]TCAATGCCCGCATCA	338692
rs374186296	snp	C/T	3.37701e-05	0.004109	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291768	TCTGGACAAACTCAT[C/T]GCAGCTCCTCGGCCC	338692
rs374201117	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292144	CCTCTCCTATCGTCT[C/G]CACCCACCTGGACAC	338692
rs374211144	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292356	TCAGACTGCCGGGGT[A/G]GTTGGGCTCCTGTGG	338692
rs374492688	snp	C/T	0.000234283	0.0108207	intron-variant	ANKRD13D	GRCh38.p7	11:67292219	TGGGTGGGATGGGGA[C/T]GGATAGCAAGAGCCA	338692
rs374540583	snp	A/G	1.78391e-05	0.00298651	intron-variant	ANKRD13D	GRCh38.p7	11:67292212	CACACCGTGGGTGGG[A/G]TGGGGACGGATAGCA	338692
rs374735254	snp	C/G/T	5.18151e-05	0.00508973	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301257	GGCTCTCCGCCAGGG[C/G/T]TCAGGCGTGGCTGTC	338692
rs374938874	snp	A/G	0.000148666	0.00862037	intron-variant	ANKRD13D	GRCh38.p7	11:67299921	CGAGACAGGGCTGGC[A/G]GGGGGCCGAGCCTGG	338692
rs374965500	snp	A/G	0.000286222	0.0119595	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301464	CCCCGCGGGTTGAGC[A/G]TGGCCCCTCTGCCAC	338692
rs374992605	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67296561	TAATGCTTTTTATTT[C/T]TGTTGCTCCCCTCTT	338692
rs375037564	snp	C/T	5.06658e-05	0.00503293	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301612	CCTGCAGTTCGCCAT[C/T]CAGCAGAGCCTGCTT	338692
rs375040408	snp	C/T	7.30807e-05	0.00604442	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301774	ACCCGGCCCGGTGCC[C/T]GCCCTCCTCCCCAGG	338692
rs375239214	snp	C/T			synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300100	CATTGGCCGCCCCAT[C/T]GAGATGTCCAGCAAA	338692
rs375491790	snp	G/T	5.0446e-05	0.005022	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301410	TCAGGTACCCCAACG[G/T]GAGGAAGAGGGAGCC	338692
rs375585353	snp	C/T	0.00118102	0.0242717	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301131	GCGCCTTCCACCTGG[C/T]TTCCCCGTCAAAATT	338692
rs375761844	snp	A/C/T	0.000788051	0.0198347	intron-variant	ANKRD13D	GRCh38.p7	11:67299784	TGGGCAGGGGCGATG[A/C/T]GAGCATTGTGACCCC	338692
rs375940543	snp	A/C/T	5.90162e-05	0.00543182	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290441	CTGCTCAACAAACTT[A/C/T]GCCAGGTACAGCAGG	338692
rs376036145	snp	A/G	0.000196406	0.00990779	intron-variant	ANKRD13D	GRCh38.p7	11:67299650	CTGCCCGGTCACACC[A/G]TGTGGTGGGGTCACC	338692
rs376291095	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291646	CGATGTGTACCGCGT[A/G]TGGAAGCGGGGTGAG	338692
rs376305629	snp	A/G	1.65018e-05	0.00287239	intron-variant	ANKRD13D	GRCh38.p7	11:67299010	AGGAAGGCTTTGGCC[A/G]GCGTGTGAGGGTGCA	338692
rs376389455	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293717	AGTTATTTGTAGAGA[C/T]AGAGTCTACAGACTG	338692
rs376430808	snp	A/C	0.00597247	0.0543191	intron-variant	ANKRD13D	GRCh38.p7	11:67295570	TCTCTACTAAAAATA[A/C]AAAAACAAAAAAAAA	338692
rs376454786	snp	C/G	0.000121795	0.00780274	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302324	CAGCTGTCACTCACT[C/G]AGCACTGAGCCATAG	338692
rs376467743	snp	A/G	1.73604e-05	0.00294616	intron-variant	ANKRD13D	GRCh38.p7	11:67292188	TTTGAGAGGTCGGTC[A/G]GGTCCTGGCACACCG	338692
rs376543024	snp	A/G/T	0.000128622	0.00801848	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291986	CCACCCCTACCGGCC[A/G/T]GCAGAGGCAGGAGCC	338692
rs376674607	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67294053	GACCATAGATAAATT[A/G]GTTACTTTCTGACTC	338692
rs376716929	snp	C/T	1.65737e-05	0.00287864	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291453	CAGGCAGGGCGCTGA[C/T]AAGCAGCTCTGGTTT	338692
rs376761629	snp	C/T	3.56163e-05	0.00421982	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301684	GGTGGGCTCTGGCCT[C/T]TGCAGCCACACGGCA	338692
rs376993735	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67300652	AAAGTTTGGCAACAC[A/G]TGAGCTGGTGACCAG	338692
rs377091252	snp	A/C	0.000437904	0.0147905	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290181	TTCGACACAATGCCA[A/C]CGTGGGCAAAGAGAA	338692
rs377166589	snp	A/G	8.28672e-05	0.00643636	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301060	GTGACCCCCATCATC[A/G]ACCTAATGGCCATCA	338692
rs377173016	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293461	TATATCTTCTTTGCA[A/G]AAATGTCTATTCAGA	338692
rs377389297	snp	A/G	0.000115855	0.00761012	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300046	AGCCATCTCCCCTGA[A/G]GAGTACTTCGACCCC	338692
rs377421834	snp	C/T	0.000310726	0.0124606	intron-variant	ANKRD13D	GRCh38.p7	11:67299819	CAGCTCCCACCCCTT[C/T]TCCGTAGCGGGGAAG	338692
rs377483619	snp	C/G	1.72967e-05	0.00294076	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301246	GAGGCACAGGTGGCT[C/G]TCCGCCAGGGCTCAG	338692
rs377512668	in-del	-/GAG			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302639	CAGTTGTAAAATGAG[-/GAG]ACCACCCCCCACCCT	338692
rs377577130	snp	C/T	4.95364e-05	0.00497652	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291641	CCAAGCGATGTGTAC[C/T]GCGTGTGGAAGCGGG	338692
rs386352277	snp	G/T			missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290346	AGGCAGTCAGCACTG[G/T]AGACCCCGAGATGGT	338692
rs527512028	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67292702	AAAGCATACAGTTCA[A/G]TGACTTTTAGTATAT	338692
rs527573062	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299312	CATGGGCCCCTACCC[A/G]GGGTACCGAGATCAA	338692
rs527585646	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298725	AAAAATGTTTCCTAG[A/G]GTGTGTCAAAGCTCA	338692
rs528100268	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298163	GCCTCCGATGTTCAC[A/G]CCATTCTCCTGCCTC	338692
rs528161874	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297564	GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	338692
rs528174103	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302842	GCCTGGGTCCCCAGG[A/C]ACCATTCACCTCCAG	338692
rs528599898	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288802	AGTGGCGTCTGCTCG[C/T]TGCTCGTCTCCAGGC	338692
rs528613340	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67296886	CTTGGCCTCCCAAAG[C/T]ACTGACATTACAGGT	338692
rs529116803	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287593	AGTGGTGAGAGCTGG[C/T]TCTAAAGTGATTGCC	338692
rs529202314	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67294400	TTAAGTCTTCTAATC[C/T]GTGAACATGGGATGT	338692
rs529278115	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300314	CTTGGCACAGAAAAC[C/T]GGTAGTTTGTCTTTG	338692
rs529282345	snp	C/T	5.48652e-05	0.00523733	intron-variant	ANKRD13D	GRCh38.p7	11:67299814	CTTACCAGCTCCCAC[C/T]CCTTCTCCGTAGCGG	338692
rs529296943	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67293634	GGACTACAGGTGCAT[A/G]CTGCCATGCCCAGCT	338692
rs529339315	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67299906	GAGCCGGGGCTGGGC[C/T]GAGACAGGGCTGGCG	338692
rs529766998	snp	C/T	9.49677e-05	0.0068902	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291959	CCCAGCACTGATTTG[C/T]GCCCCCTCTGTCCAC	338692
rs529823501	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299225	CCTGGGCTCTGGAAA[C/T]CCTGAGCATTTGTGG	338692
rs529847237	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67300739	CCTGGCACCTGGCCT[C/T]CTTGTCCAGACCAGA	338692
rs529943722	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298570	GGAGTCTCCAACTGA[A/C]ATACTTTTCTTTTAG	338692
rs530326974	snp	A/G			synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292082	GGAGCCCGAAACACT[A/G]CTGGCCGCCATGCGG	338692
rs530355434	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290952	TTGAGGCTGGCCCTC[A/C]ACCTCCAGGTGCTTA	338692
rs530432253	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67289992	GTCCTTATTTCCCAC[A/G]GCGATTCCCAACCCT	338692
rs530505341	snp	C/G	0.000534581	0.0163403	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302137	CCTCCAGGAAAGCCT[C/G]CAGCTGTCCACAGAG	338692
rs530673733	in-del	-/GCCCCGCCCGCTCCGCCGCCC	0.00953873	0.0683987	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289277	CCCCGGCCCGGCGCA[-/GCCCCGCCCGCTCCGCCGCCC]GCCCCGCCCTCCCTG	338692
rs530849361	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288542	GAAACTCGCCTTCCT[C/G]TCCTGACGCTGGCAG	338692
rs530854895	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298353	AGGCATGAGCCACCG[C/T]GCCCGGACTTATTGA	338692
rs530908937	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67295814	TGTCTTGTTCTTCAT[C/T]TTAGGGGAAAAACAT	338692
rs531094175	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300441	TGGCCTGGGAGTGGA[G/T]CGTCTGCCTTGGTGG	338692
rs531212358	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292317	TGCTCAGGGGCAGGT[A/G]GGTTGCTGCAGCCCG	338692
rs531345373	in-del	-/TTTTTTTTTTTTTTT			intron-variant	ANKRD13D	GRCh38.p7	11:67298067	TTTTCTTTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGACGGAGTCTCGC	338692
rs531628505	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67293499	CTCATTTTTTATTTA[A/G]CTTAATTAACTTATT	338692
rs532012832	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291904	CCACTTGGCAGCAGG[C/T]GGCTGAGGGTACATG	338692
rs532119183	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298207	GGTGGGACTACAGGC[A/G]TCCACCACCGTGCCC	338692
rs532235919	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296949	TCTTTTTTTGCCCAC[C/T]GTGGTCAACCTAGCT	338692
rs532423485	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302905	CAAGCCCAGGCCCTG[G/T]CCCTGACTGCGGCTT	338692
rs532597446	snp	A/C			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287735	TCCAGCAGAAACAGG[A/C]TGGACTTGGGGCTGA	338692
rs532670227	snp	C/G	6.24395e-05	0.00558712	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290444	CTCAACAAACTTCGC[C/G]AGGTACAGCAGGGCA	338692
rs532866676	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296047	TGGATATTGAACCAA[C/T]CTTGCATTCCTGTGA	338692
rs533073530	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287780	TGGGGAAGAGGGTAG[C/G]TGTGGTTGGGTTGGC	338692
rs533242799	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294526	TGTTTTATTCTGTTT[G/T]TTGTTTTGTTTTGTT	338692
rs533258681	snp	A/T	0.000798403	0.0199641	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300825	TTGGGCCACGTGGCC[A/T]GGACACCAGCTCCCG	338692
rs533333283	snp	C/T	0.000716279	0.018911	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301322	TGCCCGCATCACCTT[C/T]AGCAACCTGTGTGGC	338692
rs534148409	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298303	TCCTGACCTCATGAT[C/T]CACCCCCCTTGGCTT	338692
rs534474099	snp	A/C/G/T	0.00511176	0.0503242	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302273	GAGCGGGAGCGGCGC[A/C/G/T]GGCAGCAGGAGGAGG	338692
rs534583439	snp	A/G	1.70475e-05	0.0029195	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301635	GCCTGCTTGAAGCGG[A/G]CACTGAGGCGGAGCA	338692
rs534720385	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289240	ATGGTTGCGGGGGGA[C/T]GGGGGCGCGCGCGAA	338692
rs534756917	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298377	TTATTGAGGTTTTCT[C/T]AATGGCCTAGTGTAT	338692
rs534932957	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287996	TTAAGTGCCAGTGGG[A/G]AGCTGTGTTCAAGAT	338692
rs535559156	snp	C/T	0.000110564	0.00743438	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299479	ACTGGTGAGGCTGAG[C/T]GTGGGGAGCAGGCTC	338692
rs535578950	snp	C/T	0.000208297	0.0102032	intron-variant	ANKRD13D	GRCh38.p7	11:67292187	CTTTGAGAGGTCGGT[C/T]GGGTCCTGGCACACC	338692
rs535933469	snp	A/C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292935	TTTTGTGTCTGGCTT[A/C/T]TTTCACTTAGTATAA	338692
rs536159771	snp	C/T	0.00716266	0.059414	intron-variant	ANKRD13D	GRCh38.p7	11:67297642	GCCATTCTCCTGGCT[C/T]AGCCTCCCGAGTAGC	338692
rs536470268	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297132	TTGTCTTAACATGGA[A/G]GGTTAGGTTAAGGTT	338692
rs536509278	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293111	ACTCTAAGTATTCAT[A/G]TGCAAGTTTTTGTGT	338692
rs536595611	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290725	ACTTCAGGTTGACTC[A/G]GTGGATTATGGCCTG	338692
rs536615067	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289105	CTGTAACCGGGCACC[A/G]CCCTCCAGGCCGCCC	338692
rs536724848	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302481	TAAAGAGACTGTCGC[A/G]GCAGGGCTGCTCTGC	338692
rs536738523	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296146	TTGAGGATTTTGTGT[A/C]CATATTCATAAGTGA	338692
rs536752911	snp	C/T	3.37154e-05	0.00410568	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301597	CGAGGACGATGACCT[C/T]CTGCAGTTCGCCATC	338692
rs537139931	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288193	CCAGGACCTCACAGA[C/T]TGACACCATAGCGTG	338692
rs537221449	snp	A/C	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67294604	GGAGTGCAGTGGCAC[A/C]ATCTAGGCTCACTGC	338692
rs537402292	snp	C/T	0.000100903	0.00710221	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299547	GTACAGTGCCACCAA[C/T]GTGGAGCTGGTGACA	338692
rs537794893	snp	C/T	7.11668e-05	0.00596476	intron-variant	ANKRD13D	GRCh38.p7	11:67299949	TGGGCGGGAGGGCAC[C/T]CTCTGTCACCTTGAT	338692
rs537999687	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298328	TGGCTTCCCAAACTG[C/T]TGGGATTACAGGCAT	338692
rs538215995	snp	C/T	0.00010007	0.00707284	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292134	AGTCGCCTCACCTCT[C/T]CTATCGTCTCCACCC	338692
rs538319551	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298840	CATACCTCACAAGAT[G/T]CATGCTAATTCCTCA	338692
rs538328463	snp	A/G	0.000165599	0.0090979	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291714	ACATGACCTGGCAGC[A/G]GGGCCGGAGGAGCTT	338692
rs538353311	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290724	GACTTCAGGTTGACT[C/T]GGTGGATTATGGCCT	338692
rs538420825	snp	C/T	0.00399747	0.0445281	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290179	CCTTCGACACAATGC[C/T]AACGTGGGCAAAGAG	338692
rs538538251	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297248	GGGGTCTCACTCCAT[C/T]GCCCAGGCTGGAGTG	338692
rs538601004	snp	A/G	0.000677851	0.0183974	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302344	CTGAGCCATAGCCCC[A/G]GGAGGGCTGGCCAGG	338692
rs538802226	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67297611	GCTTACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	338692
rs538979431	snp	C/T	1.93302e-05	0.00310882	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301727	GTGGGCTCTGGTGGC[C/T]GCAGGTGACCGTCTG	338692
rs539346907	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288130	GGCTGCAGTAGTGGT[A/G]AGCAGGTGAGCTCTG	338692
rs539410597	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295322	CTCAGGAGGCTGAGG[C/G]AGGAGAATGGTGTGA	338692
rs539555529	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293767	AAGCGACCTGCCTAC[C/T]TGGGCCTCCCACAGT	338692
rs539570431	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67300528	CAGCAGGCACAGTGC[A/C]TGCACAAGCCTAGCG	338692
rs540112430	snp	C/T	0.000218126	0.0104411	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299511	GAGCCCCCAGCTCCC[C/T]GTGTCCCCTGCTCCC	338692
rs540716396	snp	A/G/T	0.000104687	0.00723414	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290401	CTACCAGAGGGCCAC[A/G/T]CAGAGGCTGGCGGGC	338692
rs540780239	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302565	TGTGGATGGCGGCCT[C/G]AGACCTGGGCTTGAA	338692
rs540789941	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296892	CTCCCAAAGCACTGA[C/T]ATTACAGGTGTGAAC	338692
rs540835703	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288269	GGGAGAAGGCAGGGT[A/G]AAAATGGCAATCAGG	338692
rs540967135	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301229	GAGAGCTGCAGGGGC[C/T]GGAGGCACAGGTGGC	338692
rs540987405	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	ANKRD13D	GRCh38.p7	11:67300785	TCCTCAGGAGCCCCA[A/G]CCTGGGCCCAGGGAG	338692
rs541078531	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291111	TCCTGTAATCCCAGC[A/G]CTTTCTGAGGCCAAA	338692
rs541177457	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67295183	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	338692
rs541298032	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287741	AGAAACAGGCTGGAC[G/T]TGGGGCTGAGTGAGG	338692
rs541601823	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292636	TTAAAAAAAAAAACA[A/G]AAAACCTTTATTGAG	338692
rs541986741	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67299704	GTTTCCCAGGATGAG[C/G]TGGGAGGCCTCCCCA	338692
rs541999135	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299254	GGGAACTCAGCGGGC[C/T]TGAGTGCCCAGCCCC	338692
rs542075222	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298952	GAGAAGGGGCCCTGA[A/G]AGTTGGGCACCCCGG	338692
rs542092419	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298361	GCCACCGCGCCCGGA[A/C]TTATTGAGGTTTTCT	338692
rs542139134	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290968	ACCTCCAGGTGCTTA[C/G]AGCCTCATTGTCTGA	338692
rs542155158	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298141	CTGTCTGCTCACTGC[A/G]AGCTCTGCCTCCGAT	338692
rs542618241	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67289696	CACGATCCCAAGCCC[A/G]GGTCACCGGCCCCTC	338692
rs542736442	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296808	TTCTTTTTTTGTAGA[A/G]ATGTGGTCTCACTAT	338692
rs542909677	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290218	GGGCTGGGCAGGTAC[C/T]GCAGAGGACAAGGGG	338692
rs543151060	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13D	GRCh38.p7	11:67295821	TTCTTCATCTTAGGG[A/G]AAAAACATTCAGTCT	338692
rs543185904	snp	C/G/T	0.00184052	0.0302804	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301772	ACACCCGGCCCGGTG[C/G/T]CCGCCCTCCTCCCCA	338692
rs543216982	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67295011	TTTAACATATAAGAT[A/T]ATGTTATCTGTAAAT	338692
rs543291312	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67300589	AGCCACCCAACAGTC[A/G]CTGGGATTCGAACCC	338692
rs543679239	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294281	GTAGGCAGAATATAT[C/G]AATTCTAGATTCAGC	338692
rs543741979	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300234	CTGGCTTCTCTCTGG[A/G]CTCCACTCCTGGAGG	338692
rs543835410	snp	A/G	0.0178098	0.0926698	intron-variant	ANKRD13D	GRCh38.p7	11:67298419	GTGTTCCGTGTGCGC[A/G]TGAGAAGCGTGTGTG	338692
rs543848729	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291317	GAGCCGAGATTGCAC[C/G]ACTACACTCCAGCCT	338692
rs544273679	snp	A/G	0.000149662	0.0086492	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299151	TAGGGGTGGGGGGCT[A/G]GGGGTAGGAGATGAG	338692
rs544500708	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297415	GCACAGGCTGGTCTC[A/G]AACTCCTGTGCTCAA	338692
rs544612782	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302684	GCTGAAAGGAGCTGG[C/T]GAGAGTCACGTGTCC	338692
rs544764472	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290929	CTCTGCACAGGCTCA[C/T]GGCCAGGTTGAGGCT	338692
rs544890068	snp	C/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289336	GCTGCCGCCGCCGCC[C/G]CCGCCGCCGCTACTG	338692
rs544951373	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288429	AAAACCAGGGCCCCA[C/G]ACCCCAGGCTGGGCC	338692
rs545035700	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13D	GRCh38.p7	11:67295622	GCACCTGTAGTCCCA[A/G]CTGCTTGGGAGACTG	338692
rs545058578	in-del	-/C	0.0236746	0.106192	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289239	ATGGTTGCGGGGGGA[-/C]CGGGGGCGCGCGCGA	338692
rs545092792	snp	C/G/T	0.000414808	0.0143959	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301250	CACAGGTGGCTCTCC[C/G/T]CCAGGGCTCAGGCGT	338692
rs545242835	snp	C/G	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67294295	TGAATTCTAGATTCA[C/G]CTTGTCAATTTCTAC	338692
rs545517854	snp	A/G	0.000399281	0.0141238	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300840	AGGACACCAGCTCCC[A/G]GGGGAGGCGGGCAGC	338692
rs545785150	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287439	TAGGAAGGAGCCATG[C/T]CTGGAGGCACTGAAT	338692
rs545982952	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293470	TTTGCAGAAATGTCT[A/G]TTCAGATCCTTTACT	338692
rs546070128	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292344	CCCGTGTCTCACTCA[G/T]ACTGCCGGGGTGGTT	338692
rs546133728	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291858	GAAGCTGAGGTTGGG[A/G]ATGGAGGGGCATCCA	338692
rs546145886	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291110	CTCCTGTAATCCCAG[C/T]GCTTTCTGAGGCCAA	338692
rs546213864	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290675	GCCTTGCCAGCTTTG[G/T]GCCTCCTGAAGAATG	338692
rs546213977	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298175	CACGCCATTCTCCTG[C/T]CTCAGCCTCCCAAGT	338692
rs546320784	snp	C/T	0.00478085	0.0486577	intron-variant	ANKRD13D	GRCh38.p7	11:67297566	AGTCTTGCTCTGTCG[C/T]CCAGGCTGGAGTGCA	338692
rs546485098	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302278	GGAGCGGCGCGGGCA[C/G]CAGGAGGAGGAGGAC	338692
rs546516305	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299261	CAGCGGGCCTGAGTG[C/T]CCAGCCCCTGCGGAG	338692
rs546768910	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302863	TCACCTCCAGCTGGG[A/G]AGAGCCCCGACGCCG	338692
rs546835024	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288858	ACTTCACCCGCACAC[C/G]CCAGCAGAGTCGGTG	338692
rs547117441	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67289743	CCTCCTCTCCCCTGC[G/T]CTGGGCCTTGCCCTG	338692
rs547354188	snp	C/T	6.73832e-05	0.00580405	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301451	TCTGGTCACCAAGCC[C/T]CGCGGGTTGAGCGTG	338692
rs547407735	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293639	ACAGGTGCATGCTGC[C/T]ATGCCCAGCTAATTT	338692
rs547416692	snp	C/T	0.0001058	0.00727245	intron-variant	ANKRD13D	GRCh38.p7	11:67300965	CCAGCCGTGCCTCAC[C/T]CATGTCCTGTGGTCG	338692
rs547524138	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296953	TTTTTGCCCACCGTG[A/G]TCAACCTAGCTAAAG	338692
rs547655499	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287798	TGGTTGGGTTGGCTT[C/T]GGACATACTGATGGG	338692
rs547839566	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300364	CATGTATGGTTTTCT[A/G]TTGAATTTCATGAGT	338692
rs548420069	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298686	TTGCCAATCTTACTG[A/T]ATCTATCCTTCCTTA	338692
rs548697717	snp	C/T	0.000601383	0.01733	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302161	CACAGAGCCCAGGGG[C/T]CCAGGATCCCCTCCC	338692
rs548906174	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290646	TGGGAGAGACTGGAC[C/G]CTTTGGAAGAGAAGC	338692
rs549149064	in-del	-/GCCGCCGCCGCC	0.00438332	0.0466095	cds-indel, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289324	CCTGCCGCCCGCGCT[-/GCCGCCGCCGCC]GCCGCCGCCGCTACT	338692
rs549253243	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287954	GAGGAGGCCGTGGAA[A/G]AGGGTTGAGAAGGCA	338692
rs549265867	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295233	CCATCCTGGCTAACA[G/T]GGTGAAACCCCATCT	338692
rs549981712	snp	A/G			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287883	CTGGGGGTGGCATCA[A/G]GGTGACAATGGGAAC	338692
rs550099152	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292917	ATTTTATAATATGTT[A/G]CCTTTTGTGTCTGGC	338692
rs550381557	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291925	AGGGTACATGATCGC[C/T]CTCTCTGCACTGCTG	338692
rs550520492	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67297618	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	338692
rs550631309	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302913	GGCCCTGGCCCTGAC[C/T]GCGGCTTGTTCTCTG	338692
rs550690116	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291249	GTGGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG	338692
rs550998629	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296492	ACTAGGAATTTGTCC[A/G]TTTCATCTAAATTAT	338692
rs551106252	snp	C/T	8.37851e-05	0.0064719	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301574	GAGCGCAACGAGCCC[C/T]TCCGGGACGAGGACG	338692
rs551311172	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302017	TCTGCTTGCCACCCT[A/G]TCTTTGCCTTTGTCC	338692
rs551334823	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288976	CCGCCGCGCACGCGC[C/G]TGCACTACCGAGGGG	338692
rs551385138	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295200	AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA	338692
rs551586785	snp	A/G	0.000150917	0.00868537	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301392	AGCTCTGCTGTTGCC[A/G]CATCAGGTACCCCAA	338692
rs551678736	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300396	CCTGCTGGGGCCAGC[A/G]TGGCACAGTGGGAAG	338692
rs552222098	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299352	GTGTTCCTCTTGACC[C/T]TGGGGCTGCATCTCC	338692
rs552457042	snp	C/T	8.35848e-05	0.00646416	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301311	CACGTGCTCAATGCC[C/T]GCATCACCTTCAGCA	338692
rs552535003	snp	C/T	0.00020029	0.0100053	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292073	CACTCTGCAGGAGCC[C/T]GAAACACTGCTGGCC	338692
rs552744411	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297209	CATTTATACTTCTAG[A/G]CATGTCTTTTCTTTT	338692
rs552748613	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289241	TGGTTGCGGGGGGAC[C/G]GGGGCGCGCGCGAAG	338692
rs553354864	snp	G/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67293412	TGATGACTAATGATG[G/T]TGAGCATCTTTTCAT	338692
rs553426701	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287424	CTGGCCGGAGGACTA[C/T]AGGAAGGAGCCATGC	338692
rs553569575	in-del	-/C	0.0054377	0.0518583	utr-variant-5-prime, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67289436	GAAGCCGAGGCGGGG[-/C]CGGGATGCGGCGCTG	338692
rs553803240	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67294736	AGAGAGACAGGATTT[C/G]ACCATGTCGGACCAG	338692
rs553809631	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67300508	TGAGCAGGTATAGGC[A/G]GTAACAGCAGGCACA	338692
rs553957683	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298936	CTCCATGTTTCATAG[C/G]GAGAAGGGGCCCTGA	338692
rs554018600	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298391	TTAATGGCCTAGTGT[A/G]TGGCCTTGAAGAGTG	338692
rs554042565	snp	C/T	1.66012e-05	0.00288103	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290381	CTGGTGCTCCAGTAT[C/T]GGGACTACCAGAGGG	338692
rs554337891	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292282	CCTGGTTCAGGCCTC[C/T]GGGCTCACTCACAAG	338692
rs554661490	snp	A/T	0.00011363	0.00753671	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290221	CTGGGCAGGTACTGC[A/T]GAGGACAAGGGGCTC	338692
rs554881484	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290827	ATCTCATACCCCCTA[A/C]CCCAGGAGCAGGCTC	338692
rs554988344	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288844	AGCCGGGGCGCCCCA[C/T]TTCACCCGCACACCC	338692
rs554993436	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291213	AGTACAAAAATTAGC[C/T]GGGAGTGGTGGCACA	338692
rs554999838	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297654	GCTCAGCCTCCCGAG[C/T]AGCTGGGACTATAGG	338692
rs555012107	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302961	GTCACTTCCGCCTGC[C/G]TAGCTGGAAGCCCTG	338692
rs555153298	snp	C/T	3.38364e-05	0.00411303	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301170	GCTGGGCACAGGCAG[C/T]GGGAGGACCTCAGGC	338692
rs555214985	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67300676	TGACCAGCTCTGGGC[C/T]GAGGAGGAAAACGGG	338692
rs555466691	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296160	TCCATATTCATAAGT[A/G]ATATTGGTCTGTAGT	338692
rs555996331	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289130	CCGCCCCAGCGGACC[C/T]GGGCCCGACCGAGGT	338692
rs556184269	snp	C/T	0.000271753	0.0116534	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299995	GGGACCCACGCAGGC[C/T]CCCGTGCAGCAGGCA	338692
rs556647998	snp	A/G	1.65765e-05	0.00287888	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291726	AGCGGGGCCGGAGGA[A/G]CTTCATCTTCAAGGG	338692
rs556751575	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290182	TCGACACAATGCCAA[C/T]GTGGGCAAAGAGAAC	338692
rs557079696	snp	C/G/T	0.000119485	0.00772857	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301737	GTGGCTGCAGGTGAC[C/G/T]GTCTGGGAAGCCCTG	338692
rs557261876	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302693	AGCTGGCGAGAGTCA[C/T]GTGTCCTTACCAAGC	338692
rs557316920	snp	C/G	0.000259302	0.0113835	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302374	GCCACTCCCTGCCCG[C/G]TTTTGTAATTTATTT	338692
rs557568359	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298965	GAGAGTTGGGCACCC[C/T]GGGCAGGCTGGCTGG	338692
rs557660112	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67300543	CTGCACAAGCCTAGC[A/G]CTCTCCCCACCATCT	338692
rs557738650	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288136	AGTAGTGGTGAGCAG[G/T]TGAGCTCTGGGCATT	338692
rs558195851	snp	C/T	0.000104882	0.00724087	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299527	GTGTCCCCTGCTCCC[C/T]AGGTGTACAGTGCCA	338692
rs558888965	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302580	CAGACCTGGGCTTGA[A/G]TCCTGGTCATGGTCC	338692
rs558990461	snp	A/G	1.65214e-05	0.0028741	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291667	GCGGGGTGAGAGCCT[A/G]CGAGTAGACACCAGT	338692
rs559065379	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297837	GCCATAAGTTTTGAT[A/G]TGTTGTGTCTTTATT	338692
rs559090291	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302976	GTAGCTGGAAGCCCT[A/G]CCCTGCTCGCCTCCG	338692
rs559132135	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288387	GTAGGGAAAGGGAGA[A/G]TAGAGGGTCAGCCTT	338692
rs559187848	snp	C/T	0	0	intron-variant	ANKRD13D	GRCh38.p7	11:67292905	CATATGAATGGAATT[C/T]TATAATATGTTGCCT	338692
rs559306055	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295176	TAATCCCAGCACTTT[G/T]GGAGGCCGAGGTGGG	338692
rs559324438	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294419	AACATGGGATGTTTT[C/T]CCATTTATTTGGATC	338692
rs559360235	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287777	GTCTGGGGAAGAGGG[C/T]AGGTGTGGTTGGGTT	338692
rs559367982	snp	G/T	0.000798403	0.0199641	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300805	GGCCCAGGGAGGAGG[G/T]CAGCTTGGGCCACGT	338692
rs559503621	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67300507	TTGAGCAGGTATAGG[C/T]GGTAACAGCAGGCAC	338692
rs560263760	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67293310	CATCCTCATCAACAC[A/G]TCATTATTCACTCAT	338692
rs560433714	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299267	GCCTGAGTGCCCAGC[C/T]CCTGCGGAGTACACA	338692
rs560527099	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291818	GGAGGACGGTGCTGC[C/T]TTTTCTCTCCACTTT	338692
rs560529148	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298150	CACTGCGAGCTCTGC[C/T]TCCGATGTTCACGCC	338692
rs560595338	snp	G/T	0.145305	0.227022	intron-variant	ANKRD13D	GRCh38.p7	11:67297526	CTCATAAGTTTTTTG[G/T]TTTTTTTTTTTTTTT	338692
rs560605905	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302734	TGAAAGTCAGATCCC[C/T]TGTGCCCTGTCCCAC	338692
rs560900255	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292299	GGCTCACTCACAAGG[A/G]GCTGCTCAGGGGCAG	338692
rs561195857	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288659	CGCTGCCTGGGCCTG[A/C]GCCCCTCTCTCCCCG	338692
rs561342169	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296877	TCCTCCTGCCTTGGC[C/G]TCCCAAAGCACTGAC	338692
rs561342525	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67289708	CCCAGGTCACCGGCC[C/T]CTCGCGCCTGAGCCT	338692
rs561453787	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301857	TGGCTGGGTCCCTGT[C/T]CCCCCAGCCCTGGCT	338692
rs561732882	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300289	ATGGTCCTCAGCCCT[C/T]AGCAAGGGGCTTGGC	338692
rs561915185	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287550	TGCCATGCTCAGGGA[C/G]CCCTTGAAGGTGCGG	338692
rs561929044	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295047	TAGTTGTATTTCTTC[C/T]TTTCCAATTTAGGTG	338692
rs562153780	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298642	ATAATGTACTTACTC[A/G]TCACCCAGCTTCAAC	338692
rs562416176	snp	A/G	8.31428e-05	0.00644705	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299152	AGGGGTGGGGGGCTG[A/G]GGGTAGGAGATGAGG	338692
rs562688615	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298534	TCTAGTTGTTCTATC[C/T]CTTATTGAAAGTGGG	338692
rs562942195	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298086	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	338692
rs563101972	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290572	CCACCAGCAAGGAGG[C/T]CTGTCTATCTTGACC	338692
rs563161431	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297483	TACAGGCGTGAGCCA[C/G]CGGGCCTGGCCTGGC	338692
rs563176227	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302051	AAAGCCGGTCCCCAG[C/T]CCCTCGGCTTCTGCC	338692
rs563273856	snp	A/G	0.00349853	0.0416776	utr-variant-5-prime, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67289433	CCCGAAGCCGAGGCG[A/G]GGCCGGGATGCGGCG	338692
rs563290860	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297948	CTTTCTACATATTTG[C/T]GAATTTCCAAAGTTT	338692
rs563336098	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288466	AATCAAGGGCCGGAA[A/C]TGAGCTGACGGAGGC	338692
rs563430838	in-del	-/TTT	0.00398564	0.0444627	intron-variant	ANKRD13D	GRCh38.p7	11:67297361	ACAGGCGCCAGCTAA[-/TTT]TTTCTGTTTTTAGTA	338692
rs563561110	snp	A/G	0.00716266	0.059414	intron-variant	ANKRD13D	GRCh38.p7	11:67295169	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG	338692
rs564312056	snp	A/G	6.67635e-05	0.00577731	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300166	TGCCTCGGGACAAGG[A/G]CTCTTGCAGACCCCT	338692
rs564481580	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299369	GGGGCTGCATCTCCT[C/T]GTTGGTGACTTCCTG	338692
rs564526871	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291894	CAAGACTGACCCACT[C/T]GGCAGCAGGTGGCTG	338692
rs564685454	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299406	AGACCCTGCCACCTC[C/T]TCCATTTTGGGGAGC	338692
rs564707226	in-del	-/AG	0.00557542	0.0525036	intron-variant	ANKRD13D	GRCh38.p7	11:67296653	TTTTGTTTTTGAGAC[-/AG]AGTCTTACTCTGTCA	338692
rs564941424	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296899	AGCACTGACATTACA[A/G]GTGTGAACCACCGCC	338692
rs564961209	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298195	GCCTCCCAAGTAGGT[A/G]GGACTACAGGCGTCC	338692
rs565406135	snp	C/T	5.41287e-05	0.00520206	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290421	GGCTGGCGGGCATTC[C/T]GGAACTGCTCAACAA	338692
rs565467958	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67289761	GGGCCTTGCCCTGCT[C/G]GCCCGAACTCGCTTC	338692
rs565469979	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297395	AGATGGGGTTTCACC[A/G]TGTTGCACAGGCTGG	338692
rs565482850	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296904	TGACATTACAGGTGT[C/G]AACCACCGCCCCCAG	338692
rs565539104	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301943	ACCCTCTGTCAGCAG[C/T]GCTATCTGCCACCAA	338692
rs565595075	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67300526	AACAGCAGGCACAGT[A/G]CCTGCACAAGCCTAG	338692
rs565655150	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295305	GCCTGTAATCCCAGC[A/T]ACTCAGGAGGCTGAG	338692
rs565711671	snp	C/T	0.000309177	0.0124295	intron-variant	ANKRD13D	GRCh38.p7	11:67300979	CCCATGTCCTGTGGT[C/T]GGCTGGGCAGGTTCA	338692
rs565801082	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293745	CTGGTCTTAAACTCT[C/T]AGGCTGAAGCGACCT	338692
rs565975198	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299508	TCTGAGCCCCCAGCT[A/C]CCCGTGTCCCCTGCT	338692
rs566055236	snp	A/G	0.00398564	0.0444627	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300412	TGGCACAGTGGGAAG[A/G]GCCCCCAGCGACGTG	338692
rs566719888	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67292002	GCAGAGGCAGGAGCC[C/G]TGGTGATGGAAGTGG	338692
rs566732034	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298712	CCTTACCTTTTTTAA[A/G]AATGTTTCCTAGAGT	338692
rs566850616	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67298289	GGATGGTCTCGATCT[C/T]CTGACCTCATGATCC	338692
rs566925828	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302963	CACTTCCGCCTGCGT[A/G]GCTGGAAGCCCTGCC	338692
rs566980176	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67297188	TATAGGCATTCACAC[A/G]TATTACATTTATACT	338692
rs567042911	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67296280	AGTTTGCAAATAATT[G/T]GTATTAATTTGTCTT	338692
rs567042996	snp	C/T	0.00154981	0.0277939	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302190	CCAGGACACCCCCAG[C/T]CCCCGGTCCACCCAG	338692
rs567138270	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290661	CCTTTGGAAGAGAAG[A/C]CTTGCCAGCTTTGGG	338692
rs567156787	snp	A/T	0.000475035	0.0154043	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301627	CCAGCAGAGCCTGCT[A/T]GAAGCGGGCACTGAG	338692
rs567812598	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287330	AATGGCCTTTGAGCC[A/G]GGCCTCCAGCATTGG	338692
rs567824719	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294688	TGGGATTACAGGTGC[C/T]CACCACCACTCCTTG	338692
rs567834425	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287957	GAGGCCGTGGAAGAG[A/G]GTTGAGAAGGCACTG	338692
rs567897978	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295286	GCCAGGCTTGGTGGC[A/G]GGCGCCTGTAATCCC	338692
rs567914768	snp	A/G	0.000399281	0.0141238	intron-variant, missense	ANKRD13D	GRCh38.p7	11:67300895	CCAGGCCAGGCAGAA[A/G]GTGGGTAAAGGCAGC	338692
rs568425028	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293582	TCATGGCTCATTGCA[C/T]CCTCCACCTCCCAGG	338692
rs568559913	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298894	GCTCAAGTGTCCCCC[C/T]CTGTCCAGGCACCCT	338692
rs568889812	in-del	-/GAG	0.00438332	0.0466095	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302636	CTTCAGTTGTAAAAT[-/GAG]GAGACCACCCCCCAC	338692
rs568940931	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291283	AATCACCTGAGCCCA[A/G]GGAGGCAGAGGTTGC	338692
rs569005545	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298253	TTTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT	338692
rs569095021	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67297619	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	338692
rs569198880	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302917	CTGGCCCTGACTGCG[G/T]CTTGTTCTCTGCGGG	338692
rs569538493	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13D	GRCh38.p7	11:67289805	ACCCAAGCTGAGAAC[A/G]AGAACTCTGGTCCTG	338692
rs569673626	snp	A/G	0.000132512	0.00813869	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301102	TTTGCCAAGCTGCGC[A/G]ACTTCATCACTCTGC	338692
rs569680290	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296106	TCTTTTCATATGTTG[C/G]TAGATTTGGTTGGTT	338692
rs569720123	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287868	AGCTGAAATGTGGAC[C/T]TGGGGGTGGCATCAG	338692
rs569833837	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297626	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGGCT	338692
rs570008177	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302594	AATCCTGGTCATGGT[C/T]CCCTTAGCCTATCTG	338692
rs570195647	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293796	GTGCTGGGATTACAG[A/G]CATGAGCCACCACAC	338692
rs570206113	snp	C/T	9.23967e-05	0.00679631	intron-variant	ANKRD13D	GRCh38.p7	11:67299938	GGGGCCGAGCCTGGG[C/T]GGGAGGGCACCCTCT	338692
rs570211384	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294560	TTGTTTTTTTTTTTG[A/C]GATGGAGTCTCACTC	338692
rs570555358	in-del	-/C	0.00199481	0.0315187	intron-variant	ANKRD13D	GRCh38.p7	11:67298305	TGACCTCATGATCCA[-/C]CCCCCCTTGGCTTCC	338692
rs570728458	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67292823	CCAAACTTCTTATCC[C/T]CTCTCCCAGTCCTAA	338692
rs570876737	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67298312	CATGATCCACCCCCC[C/T]TGGCTTCCCAAACTG	338692
rs571090503	snp	A/G	0.000114371	0.00756123	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290149	TCTGGGAAACCTGGA[A/G]TCTGTGAGAGTGCTC	338692
rs571395356	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302894	ACCCCTGCAGCCAAG[C/T]CCAGGCCCTGGCCCT	338692
rs571475926	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67292633	CACTTAAAAAAAAAA[A/C]CAAAAAACCTTTATT	338692
rs571586801	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296571	TATTTCTGTTGCTCC[C/T]CTCTTTCATTTCTGA	338692
rs571932644	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288080	GAGAGGGCTCAGGGA[A/T]GGGACCGCCTCTGAG	338692
rs571934489	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296023	TCTATTGATACATCA[A/G]TTGACCTATGGATAT	338692
rs572047090	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287434	GACTATAGGAAGGAG[C/T]CATGCCTGGAGGCAC	338692
rs572126977	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294120	TGCCAATATTATACT[C/G]TCTTAATCACTGTTG	338692
rs572353421	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291827	TGCTGCCTTTTCTCT[C/G]CACTTTCCAGATGTG	338692
rs572422847	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67298410	CCTTGAAGAGTGTTC[C/T]GTGTGCGCGTGAGAA	338692
rs572769544	in-del	-/C	0.00358779	0.0422022	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302868	TCCAGCTGGGAAGAG[-/C]CCCGACGCCGACCCC	338692
rs573133515	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290831	CATACCCCCTACCCC[A/G]GGAGCAGGCTCGGAG	338692
rs573390966	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302547	GGCGCTGTGGAGAGG[C/G]ACTGTGGATGGCGGC	338692
rs573508349	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301866	CCCTGTCCCCCCAGC[A/C]CTGGCTTGGCGGGGA	338692
rs573535044	snp	C/G	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67295402	AGCCTGGGCGACAGA[C/G]CAAGACTCCATCTCA	338692
rs573595201	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301214	TCAGCGCAGTCCCTG[G/T]AGAGCTGCAGGGGCC	338692
rs573613934	snp	A/G	0.00438332	0.0466095	intron-variant	ANKRD13D	GRCh38.p7	11:67300713	GGCCAGGCCCAGAGA[A/G]AAGCCCACAGCCTGG	338692
rs573642559	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290912	CAAAGGCTCCCCCAG[C/G]GCTCTGCACAGGCTC	338692
rs573805683	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295059	TTCCTTTCCAATTTA[A/G]GTGCCTTTTGTTTCT	338692
rs574298713	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13D	GRCh38.p7	11:67293997	GAAAAGACTATGTTT[C/T]TCCCACTGAATGGTC	338692
rs574384079	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293240	GACTGTTTACCAAAC[A/G]AGCTGTACTGGTTTA	338692
rs574580988	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67299646	CCTGCTGCCCGGTCA[C/T]ACCGTGTGGTGGGGT	338692
rs574664522	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298449	GTGGTTGTTATTGGG[C/T]AGAGTGTTCTAGCCT	338692
rs574701421	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295285	AGCCAGGCTTGGTGG[C/T]GGGCGCCTGTAATCC	338692
rs575072341	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13D	GRCh38.p7	11:67298103	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	338692
rs575405443	snp	C/T	0.00119737	0.0244387	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290197	CGTGGGCAAAGAGAA[C/T]CGCCAGGGCTGGGCA	338692
rs575513371	snp	C/T	0.0217697	0.102034	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67289532	TCGCGAACTGGAGGC[C/T]GCACTGCACAGCCAC	338692
rs575632197	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67296795	AGCCCAGCTAATTTT[A/C]TTTTTTTGTAGAGAT	338692
rs575807581	snp	C/G/T	0.000490242	0.0156489	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301767	GACCAACACCCGGCC[C/G/T]GGTGCCCGCCCTCCT	338692
rs576013395	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67295348	TGTGAACCCGGGAGG[C/T]AGAGCTTGCAGTGAG	338692
rs576152682	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288154	AGCTCTGGGCATTCA[C/G]AAGCCTTCGGGCTGC	338692
rs576164859	snp	A/C	0.00438332	0.0466095	upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287532	CGACATGGAGTCCAG[A/C]CCTGCCATGCTCAGG	338692
rs576189805	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67294270	CACAACCCAGTGTAG[G/T]CAGAATATATGAATT	338692
rs576256619	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300184	CTTGCAGACCCCTCT[C/T]TGGGCCTGTCATAGT	338692
rs576288727	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13D	GRCh38.p7	11:67293147	TATGTTTTAATTTCT[C/G]TTTCATATGTTTTCA	338692
rs576355200	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293494	CTTTACTCATTTTTT[A/T]TTTAACTTAATTAAC	338692
rs576697006	snp	A/G	0.000101425	0.00712055	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299542	CAGGTGTACAGTGCC[A/G]CCAACGTGGAGCTGG	338692
rs577247293	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67294732	TTTTAGAGAGACAGG[A/G]TTTCACCATGTCGGA	338692
rs577351881	snp	A/G	1.65326e-05	0.00287507	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291690	ACACCAGTCTCCTGG[A/G]CTTCGAGCACATGAC	338692
rs577457623	snp	C/T	0.0236746	0.106192	utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67289308	CGCCCGCCCCGCCCT[C/T]CCTGCCGCCCGCGCT	338692
rs577464141	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302643	TGTAAAATGAGGAGA[A/C]CACCCCCCACCCTCC	338692
rs577741941	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293939	GTGTATAGTGGAAGG[G/T]TCTTTTGCATGTGAC	338692
rs577872544	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301690	CTCTGGCCTCTGCAG[C/T]CACACGGCAGAAGTG	338692
rs745371010	snp	G/T	1.65787e-05	0.00287907	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291450	CAGCAGGCAGGGCGC[G/T]GACAAGCAGCTCTGG	338692
rs745475139	snp	C/T	5.63618e-05	0.00530827	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302148	GCCTGCAGCTGTCCA[C/T]AGAGCCCAGGGGCCC	338692
rs745478896	snp	C/T	1.73525e-05	0.0029455	intron-variant	ANKRD13D	GRCh38.p7	11:67300972	TGCCTCACCCATGTC[C/T]TGTGGTCGGCTGGGC	338692
rs745528580	snp	C/G			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299374	TGCATCTCCTCGTTG[C/G]TGACTTCCTGGGGTT	338692
rs745586530	snp	A/G	1.66999e-05	0.00288958	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292070	GCTCACTCTGCAGGA[A/G]CCCGAAACACTGCTG	338692
rs745761823	snp	C/T	1.68038e-05	0.00289855	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301484	CCCTCTGCCACCTGC[C/T]TAGGGAACCCTTTCC	338692
rs745876616	snp	C/G	1.67539e-05	0.00289425	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301572	TGGAGCGCAACGAGC[C/G]CCTCCGGGACGAGGA	338692
rs745917951	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67294423	TGGGATGTTTTTCCA[A/T]TTATTTGGATCTTCT	338692
rs745933553	snp	A/G	0.00011565	0.00760339	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300082	CAGCCTGGAGTCACG[A/G]AACATTGGCCGCCCC	338692
rs745957703	snp	A/G	1.65743e-05	0.00287869	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291724	GCAGCGGGGCCGGAG[A/G]AGCTTCATCTTCAAG	338692
rs746016813	snp	A/C/G	5.6761e-05	0.00532708	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291960	CCAGCACTGATTTGC[A/C/G]CCCCCTCTGTCCACC	338692
rs746025352	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293023	ATTGTATGAATATAC[C/T]ATATCTTGTTTATTC	338692
rs746109879	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296528	TTGTTGGTGTACAGC[C/T]ATCATTGTATCCTTT	338692
rs746135795	snp	C/T	5.0053e-05	0.0050024	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301316	GCTCAATGCCCGCAT[C/T]ACCTTCAGCAACCTG	338692
rs746236702	snp	A/G	3.33072e-05	0.00408075	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299157	TGGGGGGCTGGGGGT[A/G]GGAGATGAGGTCCAG	338692
rs746254978	snp	C/T			missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291612	CTGCAGTGCCCCTTG[C/T]GTCTAAGATGTGCCC	338692
rs746309255	snp	A/G			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287921	CTCTCTCCCAGGGAT[A/G]TGGGGGTCAGGGAGA	338692
rs746328789	snp	C/T	9.73378e-05	0.00697563	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299600	CTGATCAGGACAAGT[C/T]GAGGAGCAAAGGTAA	338692
rs746414702	snp	A/C	5.7852e-05	0.00537798	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290438	GAACTGCTCAACAAA[A/C]TTCGCCAGGTACAGC	338692
rs746499236	snp	C/T	0.000105302	0.00725534	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290284	AGCCAGGCCTGGGGT[C/T]ATCTGGAGGGCTCCC	338692
rs746524696	snp	C/T	6.36011e-05	0.00563884	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299563	GTGGAGCTGGTGACA[C/T]GCACACGCACGGAGC	338692
rs746574933	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290581	AGGAGGTCTGTCTAT[C/T]TTGACCCCAGCCCAG	338692
rs746613610	in-del	-/GGGGGG			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299142	GGAGAGGCTAGGGGT[-/GGGGGG]GGGGGGCTGGGGGTA	338692
rs746618627	snp	A/G	0.000216556	0.0104034	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290422	GCTGGCGGGCATTCC[A/G]GAACTGCTCAACAAA	338692
rs746689096	snp	A/G	1.66059e-05	0.00288144	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301819	GAACAGCTTCAGCTG[A/G]AGCGGTGAGCCCCTC	338692
rs746722680	snp	A/G	3.31554e-05	0.00407144	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300128	AAAGTACAGAGGTGA[A/G]GTCTGAGAGCTGGCT	338692
rs746737297	in-del	-/AGG	0.000247698	0.011126	upstream-variant-2KB, cds-indel, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302280	AGCGGCGCGGGCAGC[-/AGG]AGGAGGAGGACTTAC	338692
rs746799045	snp	C/G/T	5.55945e-05	0.00527207	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291977	CCCCTCTGTCCACCC[C/G/T]TACCGGCCGGCAGAG	338692
rs746872366	snp	A/G	0.000428965	0.0146389	intron-variant	ANKRD13D	GRCh38.p7	11:67299026	GCGTGTGAGGGTGCA[A/G]GTCTCACCAGCTCCT	338692
rs746888903	snp	A/G	1.70624e-05	0.00292077	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292039	ACCGGCAGGTGGTGC[A/G]TGTGGAGACACTGGG	338692
rs746919741	in-del	-/TTTTGTTTTG			intron-variant	ANKRD13D	GRCh38.p7	11:67296613	AATTTGAAGTTTTTG[-/TTTTGTTTTG]TTTTGTTTTGTTTTG	338692
rs747222822	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290629	AGACGGCCAGGCTCA[C/T]GTGGGAGAGACTGGA	338692
rs747278525	snp	C/T	1.65674e-05	0.00287809	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291718	GACCTGGCAGCGGGG[C/T]CGGAGGAGCTTCATC	338692
rs747290839	snp	C/G	7.56058e-05	0.00614794	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302270	GAGGAGCGGGAGCGG[C/G]GCGGGCAGCAGGAGG	338692
rs747378704	snp	A/G	1.72695e-05	0.00293845	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301231	GAGCTGCAGGGGCCG[A/G]AGGCACAGGTGGCTC	338692
rs747606956	snp	A/G	1.83088e-05	0.00302557	intron-variant	ANKRD13D	GRCh38.p7	11:67292231	GGACGGATAGCAAGA[A/G]CCACCATTAATGAGG	338692
rs747640120	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287706	TGAAAAGAGGCCAGA[C/T]GGGAAGAACGTGGTC	338692
rs747853002	snp	C/T	1.70627e-05	0.00292079	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301638	TGCTTGAAGCGGGCA[C/T]TGAGGCGGAGCAGGT	338692
rs747896765	snp	G/T	1.8369e-05	0.00303054	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301703	AGCCACACGGCAGAA[G/T]TGACAGCTGTGGGCT	338692
rs747951763	in-del	-/CA	7.06839e-05	0.00594449	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290458	CCAGGTACAGCAGGG[-/CA]CAGTTATGGAGGTGG	338692
rs748039908	in-del	-/G	1.75462e-05	0.00296189	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301672	ACTTGCCCAGGGGGT[-/G]GGCTCTGGCCTCTGC	338692
rs748058712	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296814	TTTTGTAGAGATGTG[G/T]TCTCACTATGTCATC	338692
rs748151356	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67300588	TAGCCACCCAACAGT[C/T]GCTGGGATTCGAACC	338692
rs748157475	snp	C/T	0.000150566	0.00867526	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291964	CACTGATTTGCGCCC[C/T]CTCTGTCCACCCCTA	338692
rs748241226	snp	C/T	1.68343e-05	0.00290118	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301469	CGGGTTGAGCGTGGC[C/T]CCTCTGCCACCTGCC	338692
rs748354816	snp	C/T	4.96323e-05	0.00498133	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291481	TTTCTCTTAGGCCCC[C/T]GATTTCTACGTTGAG	338692
rs748410932	in-del	-/TTTTTTTTTTTTTT			intron-variant	ANKRD13D	GRCh38.p7	11:67298059	TATTGAGGTTTTCTT[-/TTTTTTTTTTTTTT]TTTTTTTTTGAGACG	338692
rs748418860	snp	A/G	1.8391e-05	0.00303235	intron-variant	ANKRD13D	GRCh38.p7	11:67299902	GGGTGAGCCGGGGCT[A/G]GGCCGAGACAGGGCT	338692
rs748459789	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67289749	CTCCCCTGCGCTGGG[C/T]CTTGCCCTGCTCGCC	338692
rs748528423	snp	A/G	9.76086e-05	0.00698533	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302167	GCCCAGGGGCCCAGG[A/G]TCCCCTCCCAGGACA	338692
rs748529661	snp	A/G	1.65111e-05	0.0028732	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291635	ATGTGCCCAAGCGAT[A/G]TGTACCGCGTGTGGA	338692
rs748581543	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291922	CTGAGGGTACATGAT[C/T]GCCCTCTCTGCACTG	338692
rs748616231	snp	C/G	6.66067e-05	0.00577052	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302248	GGAGTTGTCTTCACG[C/G]GAGCAGGAGGAGCGG	338692
rs748646221	snp	C/T	1.65647e-05	0.00287786	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301099	CACTTTGCCAAGCTG[C/T]GCGACTTCATCACTC	338692
rs748649183	snp	C/T	3.41122e-05	0.00412976	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301192	ACCTCAGGCATGGCA[C/T]CCTCCCTCAGCGCAG	338692
rs748792420	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67300575	AGGAGGATTCTCTTA[G/T]CCACCCAACAGTCGC	338692
rs748815373	snp	C/T	1.65641e-05	0.00287781	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301082	TGGCCATCAGCAACG[C/T]TCACTTTGCCAAGCT	338692
rs748897038	snp	A/G	3.38771e-05	0.00411551	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301176	CACAGGCAGCGGGAG[A/G]ACCTCAGGCATGGCA	338692
rs748985192	snp	A/C/G	3.61084e-05	0.0042489	intron-variant	ANKRD13D	GRCh38.p7	11:67292220	GGGTGGGATGGGGAC[A/C/G]GATAGCAAGAGCCAC	338692
rs748995946	snp	A/G	5.42138e-05	0.00520614	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301696	CCTCTGCAGCCACAC[A/G]GCAGAAGTGACAGCT	338692
rs749097377	snp	A/G	1.67728e-05	0.00289588	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301578	GCAACGAGCCCCTCC[A/G]GGACGAGGACGATGA	338692
rs749167372	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67294740	AGACAGGATTTCACC[A/G]TGTCGGACCAGGCTG	338692
rs749187440	snp	C/T	1.70107e-05	0.00291634	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301632	AGAGCCTGCTTGAAG[C/T]GGGCACTGAGGCGGA	338692
rs749273051	in-del	-/G	9.20231e-05	0.00678256	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290251	CCCCTGAGGCTGGCA[-/G]GGCGGGGGGCAGTGA	338692
rs749427074	snp	C/G	1.67947e-05	0.00289777	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301404	GCCGCATCAGGTACC[C/G]CAACGGGAGGAAGAG	338692
rs749569602	snp	A/G	3.36927e-05	0.00410429	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301455	GTCACCAAGCCCCGC[A/G]GGTTGAGCGTGGCCC	338692
rs749637693	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290620	AGGAAAGAGAGACGG[C/G]CAGGCTCACGTGGGA	338692
rs749646994	snp	G/T	0.000181373	0.00952122	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290442	TGCTCAACAAACTTC[G/T]CCAGGTACAGCAGGG	338692
rs749656378	snp	C/T	1.83102e-05	0.00302568	intron-variant	ANKRD13D	GRCh38.p7	11:67299799	CGAGCATTGTGACCC[C/T]TTACCAGCTCCCACC	338692
rs749678530	snp	A/C			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288025	ATGGCAGAAATCAGG[A/C]GAGGCTGGAACCAAG	338692
rs749774954	snp	C/G	1.67818e-05	0.00289665	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301840	TGAGCCCCTCATGGG[C/G]CTGGCTGGGTCCCTG	338692
rs749790438	snp	A/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288451	GGCTGGGCCTCCAGT[A/T]ATCAAGGGCCGGAAC	338692
rs750009823	snp	C/T	3.30611e-05	0.00406565	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291578	CCTTTGGAAAGACCC[C/T]CAGTGACCCCTGTGC	338692
rs750011657	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292668	TATAATCTCATATAC[C/T]ATATAAGATCACCCA	338692
rs750146058	snp	C/T	5.12256e-05	0.00506065	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302203	AGCCCCCGGTCCACC[C/T]AGCTTTGAAGAGCAG	338692
rs750239211	snp	C/T	1.67497e-05	0.00289389	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301567	GGGCATGGAGCGCAA[C/T]GAGCCCCTCCGGGAC	338692
rs750320304	snp	A/G	5.37062e-05	0.00518172	intron-variant	ANKRD13D	GRCh38.p7	11:67292216	CCGTGGGTGGGATGG[A/G]GACGGATAGCAAGAG	338692
rs750361664	snp	A/G	3.30671e-05	0.00406602	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299110	ATGGAAACTGTTAGC[A/G]GCTACGAGGCCAAGG	338692
rs750597441	snp	C/T	2.00294e-05	0.00316454	intron-variant	ANKRD13D	GRCh38.p7	11:67300936	CCAGAGGGCAGTCCT[C/T]AATGGAAGGGCCACC	338692
rs750628584	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296089	TGGTTGTGGTGTATA[A/G]TTCTTTTCATATGTT	338692
rs750688587	snp	C/T	1.74372e-05	0.00295268	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292026	GAAGTGGACCATGAC[C/T]GGCAGGTGGTGCATG	338692
rs750696794	in-del	-/CAGCCAGCCCCACCAACCCCA	3.36033e-05	0.00409884	cds-indel, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300009	CCCCCGTGCAGCAGG[-/CAGCCAGCCCCACCAACCCCA]CAGCCATCTCCCCTG	338692
rs750731875	snp	G/T	1.66446e-05	0.00288479	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292096	TGCTGGCCGCCATGC[G/T]GCCCAGCGAGGAGCA	338692
rs750853791	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302617	CCTATCTGAGCCTCA[A/G]TTTCTTCAGTTGTAA	338692
rs750860874	snp	A/G	3.33078e-05	0.00408078	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292089	GAAACACTGCTGGCC[A/G]CCATGCGGCCCAGCG	338692
rs750976132	snp	C/T	5.0104e-05	0.00500494	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301537	GTTTGAAGTGCCCAA[C/T]GGGTACAGCGTGCTG	338692
rs751046958	snp	A/C			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291292	AGCCCAGGGAGGCAG[A/C]GGTTGCAGTGAGCCG	338692
rs751066668	snp	A/G/T	8.42373e-05	0.00648941	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301448	CTTTCTGGTCACCAA[A/G/T]CCCCGCGGGTTGAGC	338692
rs751119070	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292563	GAACCTGACCCTTCC[A/G]GCAAGAGTTTCTCTG	338692
rs751194090	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291757	CCAGGGTGAGCTCTG[A/G]ACAAACTCATTGCAG	338692
rs751202804	snp	C/G	1.6591e-05	0.00288015	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291447	CAGCAGCAGGCAGGG[C/G]GCTGACAAGCAGCTC	338692
rs751248657	snp	A/G	1.82643e-05	0.00302189	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299864	CTTCCTGGGGATGGC[A/G]CAGCAGCATTCCTCC	338692
rs751332786	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300214	TTAGGGACCCACTCC[C/T]TCGGCTGGCTTCTCT	338692
rs751347363	snp	C/G	1.65332e-05	0.00287512	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291556	CTCCCAGGGATTTGG[C/G]GTGGGGCCTTTGGAA	338692
rs751373885	snp	G/T	1.68505e-05	0.00290258	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302105	GTTCTTCCCTCCCCT[G/T]CCCTGCCTGGAAGGG	338692
rs751402979	snp	A/C	0.000100654	0.00709345	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302192	AGGACACCCCCAGCC[A/C]CCGGTCCACCCAGCT	338692
rs751493163	snp	A/G	1.66827e-05	0.00288809	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301138	CCACCTGGCTTCCCC[A/G]TCAAAATTGGTGAGA	338692
rs751541067	snp	C/G/T	3.33002e-05	0.00408034	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292129	TGGCCAGTCGCCTCA[C/G/T]CTCTCCTATCGTCTC	338692
rs751571003	snp	A/G	0.000114896	0.00757859	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290109	AGGACCCCCGCGGGC[A/G]GACCCCACTGGAGCT	338692
rs751726088	snp	C/T	6.44808e-05	0.0056777	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290374	GGTGCAGCTGGTGCT[C/T]CAGTATCGGGACTAC	338692
rs751758780	snp	C/T	1.77707e-05	0.00298077	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301682	GGGGTGGGCTCTGGC[C/T]TCTGCAGCCACACGG	338692
rs751837119	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67295467	TAGTGGTTCACGCCT[C/G]TAATCCCAGAACTTT	338692
rs751859751	snp	C/T	4.15101e-05	0.00455558	intron-variant	ANKRD13D	GRCh38.p7	11:67300917	AAAGGCAGCTGCCCA[C/T]GAACCAGAGGGCAGT	338692
rs751935481	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67296096	GGTGTATAATTCTTT[C/T]CATATGTTGCTAGAT	338692
rs751959550	snp	C/T	1.91378e-05	0.00309331	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291942	TCTCTGCACTGCTGG[C/T]GCCCAGCACTGATTT	338692
rs752019597	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67294092	GTTCCATTGGTCTAC[A/G]TGTCTGTCTTTATGC	338692
rs752047469	snp	A/G	1.81694e-05	0.00301403	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291993	TACCGGCCGGCAGAG[A/G]CAGGAGCCCTGGTGA	338692
rs752232115	snp	C/T	1.66685e-05	0.00288686	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301372	CCGTGTGGGTGCCGG[C/T]CCCCAGCTCTGCTGT	338692
rs752246500	snp	A/G	1.68681e-05	0.00290409	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301299	ATTCCCCTTTTCCAC[A/G]TGCTCAATGCCCGCA	338692
rs752321830	snp	A/G	0.000102286	0.0071507	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299537	CTCCCCAGGTGTACA[A/G]TGCCACCAACGTGGA	338692
rs752356283	snp	C/T			missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290184	GACACAATGCCAACG[C/T]GGGCAAAGAGAACCG	338692
rs752612828	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298839	TCATACCTCACAAGA[C/T]TCATGCTAATTCCTC	338692
rs752616085	snp	A/G	0.000151023	0.00868843	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302090	GGCGCTCACTGGCCT[A/G]TTCTTCCCTCCCCTG	338692
rs752629115	snp	C/T	8.53983e-05	0.0065339	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301793	CTCCTCCCCAGGCCA[C/T]GGTTTATGAGGAACA	338692
rs752670481	snp	C/T	1.93478e-05	0.00311023	intron-variant	ANKRD13D	GRCh38.p7	11:67300947	TCCTCAATGGAAGGG[C/T]CACCAGCCGTGCCTC	338692
rs752760501	snp	A/C/G	3.54241e-05	0.00420845	intron-variant	ANKRD13D	GRCh38.p7	11:67292205	GTCCTGGCACACCGT[A/C/G]GGTGGGATGGGGACG	338692
rs752779576	snp	A/C/T	0.000105142	0.00724991	intron-variant	ANKRD13D	GRCh38.p7	11:67299974	CTTGATGGCTGAGTC[A/C/T]GCCCTGGGACCCACG	338692
rs752790224	snp	C/G			missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301063	ACCCCCATCATCGAC[C/G]TAATGGCCATCAGCA	338692
rs752854291	snp	A/C	1.6498e-05	0.00287206	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299063	TCTGTTTCAGGAACA[A/C]ATGTGGTATCTGGGG	338692
rs753008031	snp	A/C/G	0.00120819	0.024549	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301607	GACCTCCTGCAGTTC[A/C/G]CCATCCAGCAGAGCC	338692
rs753040064	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292881	GTAGAATTCCCTGCT[C/T]TGAGTTCTCATATGA	338692
rs753090373	snp	C/T	3.31153e-05	0.00406898	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291713	CACATGACCTGGCAG[C/T]GGGGCCGGAGGAGCT	338692
rs753108287	snp	G/T	1.75265e-05	0.00296023	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301670	GGACTTGCCCAGGGG[G/T]TGGGCTCTGGCCTCT	338692
rs753162888	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293729	AGATAGAGTCTACAG[A/G]CTGGTCTTAAACTCT	338692
rs753200046	snp	A/G	1.65359e-05	0.00287536	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300056	CCTGAGGAGTACTTC[A/G]ACCCCAACTTCAGCC	338692
rs753220857	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295638	CTGCTTGGGAGACTG[A/T]GGCACAAGAATTGCT	338692
rs753276055	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292588	TCTCTGACAACACAT[A/G]CCCCCTCTTGCCTTA	338692
rs753281171	snp	G/T	1.72507e-05	0.00293685	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291791	CTCGGCCCTTGGGTT[G/T]CCTGCGGCTTGGGAG	338692
rs753352237	snp	C/T	0.000119262	0.00772118	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291778	CTCATTGCAGCTCCT[C/T]GGCCCTTGGGTTTCC	338692
rs753397430	snp	A/G	0.000117103	0.007651	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302223	TTGAAGAGCAGCTGC[A/G]CCTGGCCCTGGAGTT	338692
rs753582189	snp	A/G	1.72204e-05	0.00293427	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301266	CCAGGGCTCAGGCGT[A/G]GCTGTCTTCTCACAG	338692
rs753636735	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287563	GAGCCCTTGAAGGTG[C/T]GGAACAGGGCTGAGA	338692
rs753668849	snp	A/G	0.000133107	0.00815695	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299137	AAGGCAGGAGAGGCT[A/G]GGGGTGGGGGGCTGG	338692
rs753742731	snp	C/T	0.000114371	0.00756123	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290145	TGTCTCTGGGAAACC[C/T]GGAGTCTGTGAGAGT	338692
rs753827080	snp	C/G	1.7959e-05	0.00299652	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301691	TCTGGCCTCTGCAGC[C/G]ACACGGCAGAAGTGA	338692
rs753898914	snp	A/C/T	9.94806e-05	0.00705211	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301050	GGGTGACCAGGTGAC[A/C/T]CCCATCATCGACCTA	338692
rs753919339	in-del	-/C	1.67433e-05	0.00289333	upstream-variant-2KB, frameshift-variant, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301563	GCTGGGCATGGAGCG[-/C]CAACGAGCCCCTCCG	338692
rs753990181	snp	C/G	1.66286e-05	0.0028834	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292120	AGGAGCATGTGGCCA[C/G]TCGCCTCACCTCTCC	338692
rs754074883	snp	A/C			intron-variant	ANKRD13D	GRCh38.p7	11:67299739	CGTCTGACCCCTCTT[A/C]CCCCAGACAGTAGGC	338692
rs754079696	snp	C/T	3.51883e-05	0.00419439	intron-variant	ANKRD13D	GRCh38.p7	11:67292201	TCGGGTCCTGGCACA[C/T]CGTGGGTGGGATGGG	338692
rs754237889	snp	C/G	1.82951e-05	0.00302443	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299878	CGCAGCAGCATTCCT[C/G]CCACACCGGGGTGAG	338692
rs754248697	snp	A/G	1.67332e-05	0.00289246	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301561	CGTGCTGGGCATGGA[A/G]CGCAACGAGCCCCTC	338692
rs754473239	snp	A/G	1.69974e-05	0.0029152	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301184	GCGGGAGGACCTCAG[A/G]CATGGCACCCTCCCT	338692
rs754549964	snp	C/T	1.81099e-05	0.00300909	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302329	GTCACTCACTGAGCA[C/T]TGAGCCATAGCCCCG	338692
rs754633759	snp	C/T	3.43413e-05	0.0041436	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301273	TCAGGCGTGGCTGTC[C/T]TCTCACAGAGATTCC	338692
rs754656252	snp	G/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287619	TTGCCTGGTTACTGA[G/T]TACAGGATGTGGGGA	338692
rs754684560	in-del	-/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298896	TCAAGTGTCCCCCCC[-/T]GTCCAGGCACCCTCT	338692
rs754739525	snp	C/G/T	9.96943e-05	0.00705955	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299143	GGAGAGGCTAGGGGT[C/G/T]GGGGGCTGGGGGTAG	338692
rs754994734	in-del	-/T	1.67643e-05	0.00289515	upstream-variant-2KB, frameshift-variant, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301576	CGCAACGAGCCCCTC[-/T]CGGGACGAGGACGAT	338692
rs755041159	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298739	GAGTGTGTCAAAGCT[C/T]ATCCCAGATGTCCTA	338692
rs755060538	snp	C/T	1.66313e-05	0.00288364	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292122	GAGCATGTGGCCAGT[C/T]GCCTCACCTCTCCTA	338692
rs755235157	snp	C/T	5.05651e-05	0.00502792	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301463	GCCCCGCGGGTTGAG[C/T]GTGGCCCCTCTGCCA	338692
rs755325079	snp	C/T	1.67371e-05	0.0028928	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301562	GTGCTGGGCATGGAG[C/T]GCAACGAGCCCCTCC	338692
rs755474889	snp	A/G	1.65121e-05	0.00287329	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291620	CCCCTTGTGTCTAAG[A/G]TGTGCCCAAGCGATG	338692
rs755474983	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292785	CTCAGGAAGAAACCC[C/T]CCACCCTTTAGCTAA	338692
rs755492271	snp	C/T	1.65408e-05	0.00287578	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291700	CCTGGGCTTCGAGCA[C/T]ATGACCTGGCAGCGG	338692
rs755493558	snp	A/G			missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291681	TGCGAGTAGACACCA[A/G]TCTCCTGGGCTTCGA	338692
rs755558769	in-del	-/GGC			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302557	AGAGGCACTGTGGAT[-/GGC]GGCCTCAGACCTGGG	338692
rs755633901	snp	C/T	1.65214e-05	0.0028741	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291595	AGTGACCCCTGTGCA[C/T]CCTGCAGTGCCCCTT	338692
rs755692997	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292346	CGTGTCTCACTCAGA[C/G]TGCCGGGGTGGTTGG	338692
rs755723333	snp	A/C	0.000107021	0.00731429	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302154	AGCTGTCCACAGAGC[A/C]CAGGGGCCCAGGATC	338692
rs755811448	snp	G/T	0.000208409	0.0102059	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302205	CCCCCGGTCCACCCA[G/T]CTTTGAAGAGCAGCT	338692
rs755817642	snp	C/T	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301077	CCTAATGGCCATCAG[C/T]AACGCTCACTTTGCC	338692
rs755886668	snp	A/G	1.79371e-05	0.0029947	intron-variant	ANKRD13D	GRCh38.p7	11:67292217	CGTGGGTGGGATGGG[A/G]ACGGATAGCAAGAGC	338692
rs755991871	snp	A/G	5.16774e-05	0.00508291	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301264	CGCCAGGGCTCAGGC[A/G]TGGCTGTCTTCTCAC	338692
rs756053706	snp	A/C			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287338	TTGAGCCAGGCCTCC[A/C]GCATTGGTGTGGGAA	338692
rs756117054	snp	C/T	1.6522e-05	0.00287414	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300088	GGAGTCACGGAACAT[C/T]GGCCGCCCCATCGAG	338692
rs756204776	snp	A/G	1.95349e-05	0.00312523	intron-variant	ANKRD13D	GRCh38.p7	11:67300944	CAGTCCTCAATGGAA[A/G]GGCCACCAGCCGTGC	338692
rs756267653	in-del	-/TG	6.68919e-05	0.00578286	frameshift-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301004	GGTTCAAGGCAACAC[-/TG]TGGCTGAGTGAAGAG	338692
rs756403726	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298606	TATTTTGGAAAATTT[C/T]AAACATATATGAAAG	338692
rs756412452	snp	C/T	4.99122e-05	0.00499536	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292103	CGCCATGCGGCCCAG[C/T]GAGGAGCATGTGGCC	338692
rs756537010	snp	C/G	1.6851e-05	0.00290263	upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301452	CTGGTCACCAAGCCC[C/G]GCGGGTTGAGCGTGG	338692
rs756553746	snp	A/G	1.67008e-05	0.00288965	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301538	TTTGAAGTGCCCAAC[A/G]GGTACAGCGTGCTGG	338692
rs756637146	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290584	AGGTCTGTCTATCTT[A/G]ACCCCAGCCCAGGGT	338692
rs756643487	snp	C/T	1.82877e-05	0.00302383	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299875	TGGCGCAGCAGCATT[C/T]CTCCCACACCGGGGT	338692
rs756762047	snp	A/G	1.65883e-05	0.00287991	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291446	CCAGCAGCAGGCAGG[A/G]CGCTGACAAGCAGCT	338692
rs756786939	snp	A/G	1.83199e-05	0.00302648	intron-variant	ANKRD13D	GRCh38.p7	11:67299787	GCAGGGGCGATGCGA[A/G]CATTGTGACCCCTTA	338692
rs756919492	snp	A/C	1.65348e-05	0.00287526	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291563	GGATTTGGGGTGGGG[A/C]CTTTGGAAAGACCCC	338692
rs756965841	snp	A/G	4.16536e-05	0.00456345	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301821	ACAGCTTCAGCTGGA[A/G]CGGTGAGCCCCTCAT	338692
rs756997320	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300282	CTTATCCATGGTCCT[C/T]AGCCCTTAGCAAGGG	338692
rs757059372	snp	A/C	0.00012062	0.00776501	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302106	TTCTTCCCTCCCCTG[A/C]CCTGCCTGGAAGGGC	338692
rs757198572	snp	A/T	1.67449e-05	0.00289347	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301153	GTCAAAATTGGTGAG[A/T]GGCTGGGCACAGGCA	338692
rs757393042	snp	C/T	3.43342e-05	0.00414318	intron-variant	ANKRD13D	GRCh38.p7	11:67299988	CCGCCCTGGGACCCA[C/T]GCAGGCCCCCGTGCA	338692
rs757402786	snp	A/C	1.65236e-05	0.00287429	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300071	GACCCCAACTTCAGC[A/C]TGGAGTCACGGAACA	338692
rs757513077	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298734	TCCTAGAGTGTGTCA[A/G]AGCTCATCCCAGATG	338692
rs757644851	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67296196	TGTGATATATGTCTG[A/G]TTTTGGTATCTGGGT	338692
rs757685863	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295597	AAAAATTAGCCAGGC[A/T]TGGTGGTGGGCACCT	338692
rs757711478	snp	A/G	1.80361e-05	0.00300295	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291999	CCGGCAGAGGCAGGA[A/G]CCCTGGTGATGGAAG	338692
rs757957778	snp	C/T	1.66721e-05	0.00288717	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301384	CGGCCCCCAGCTCTG[C/T]TGTTGCCGCATCAGG	338692
rs758038056	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67287394	GAAGAGCCAGGGACT[C/T]ATGAGTGGCCCAGGC	338692
rs758157475	snp	A/G	0.000115751	0.00760671	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301794	TCCTCCCCAGGCCAC[A/G]GTTTATGAGGAACAG	338692
rs758256260	in-del	-/G	5.87769e-05	0.00542079	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302227	AGAGCAGCTGCGCCT[-/G]GCCCTGGAGTTGTCT	338692
rs758309691	snp	C/T	1.89217e-05	0.00307579	intron-variant	ANKRD13D	GRCh38.p7	11:67300950	TCAATGGAAGGGCCA[C/T]CAGCCGTGCCTCACC	338692
rs758333703	snp	C/G	1.69278e-05	0.00290923	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302100	GGCCTGTTCTTCCCT[C/G]CCCTGCCCTGCCTGG	338692
rs758350230	snp	A/G			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300159	GGGGACTTGCCTCGG[A/G]ACAAGGGCTCTTGCA	338692
rs758393993	snp	G/T	0.000210815	0.0102646	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292033	ACCATGACCGGCAGG[G/T]GGTGCATGTGGAGAC	338692
rs758747467	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292608	CTCTTGCCTTAACAG[G/T]CAGTGGAAACACTTA	338692
rs758874764	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295872	GTTGTGAGTTTTTGG[A/T]AGATACCCTTCATCA	338692
rs759078568	in-del	-/CCCCCGGGTCCCC			intron-variant	ANKRD13D	GRCh38.p7	11:67289580	GGGCACCCGGCCCTT[-/CCCCCGGGTCCCC]CACCCAAGGCTGTGG	338692
rs759086172	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298216	ACAGGCGTCCACCAC[C/T]GTGCCCGGCTAATTT	338692
rs759088435	snp	A/C/G	3.40926e-05	0.0041286	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291779	TCATTGCAGCTCCTC[A/C/G]GCCCTTGGGTTTCCT	338692
rs759176852	snp	C/T	1.66651e-05	0.00288657	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301369	GCTCCGTGTGGGTGC[C/T]GGCCCCCAGCTCTGC	338692
rs759389256	snp	C/G	1.68182e-05	0.00289979	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301419	CCAACGGGAGGAAGA[C/G]GGAGCCTGCACAGCT	338692
rs759455940	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291121	CCAGCGCTTTCTGAG[A/G]CCAAAGTGGGCGGAT	338692
rs759505483	snp	A/T	1.80501e-05	0.00300411	intron-variant	ANKRD13D	GRCh38.p7	11:67299663	CCGTGTGGTGGGGTC[A/T]CCCTGGCCTGGGATT	338692
rs759550712	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291127	CTTTCTGAGGCCAAA[A/G]TGGGCGGATCACTTG	338692
rs759607456	snp	C/T	1.82757e-05	0.00302283	intron-variant	ANKRD13D	GRCh38.p7	11:67299824	CCCACCCCTTCTCCG[C/T]AGCGGGGAAGACTCC	338692
rs759793497	snp	A/G	9.97241e-05	0.0070606	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301026	GAGTGAAGAGCACCC[A/G]CTCTCCCTGGGTGAC	338692
rs759813543	snp	A/G	1.64982e-05	0.00287208	splice-acceptor-variant	ANKRD13D	GRCh38.p7	11:67299056	TGTTTGGTCTGTTTC[A/G]GGAACAAATGTGGTA	338692
rs759828211	snp	C/T	0.00013709	0.00827804	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290044	GCCTTGCCCTCTTCT[C/T]TCCTGCCCTTTGTGA	338692
rs759987568	snp	C/T	9.81595e-05	0.00700501	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290324	CTGGTGCCCGCAGTC[C/T]TGCAGGAGGCAGTCA	338692
rs760088672	snp	A/G/T	3.50442e-05	0.00418582	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301669	GGGACTTGCCCAGGG[A/G/T]GTGGGCTCTGGCCTC	338692
rs760115441	snp	C/G	1.72009e-05	0.0029326	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301649	GGCACTGAGGCGGAG[C/G]AGGTGGGACTTGCCC	338692
rs760203702	snp	A/G	3.33739e-05	0.00408483	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300020	CAGGCAGCCAGCCCC[A/G]CCAACCCCACAGCCA	338692
rs760228565	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67293600	TCCACCTCCCAGGCT[C/G]AAGTGATCTAAGTAG	338692
rs760243109	snp	C/G	3.2963e-05	0.00405961	intron-variant	ANKRD13D	GRCh38.p7	11:67299965	CTCTGTCACCTTGAT[C/G]GCTGAGTCCGCCCTG	338692
rs760281463	snp	C/T	4.96044e-05	0.00497993	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291694	CAGTCTCCTGGGCTT[C/T]GAGCACATGACCTGG	338692
rs760353360	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295327	GAGGCTGAGGCAGGA[G/T]AATGGTGTGAACCCG	338692
rs760440276	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67298252	ATTTTTTAGTAGAGA[C/T]GGGGTTTCATCATGT	338692
rs760484836	snp	C/T	3.51111e-05	0.00418979	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302315	CGGATCCTGCAGCTG[C/T]CACTCACTGAGCACT	338692
rs760650362	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288685	CCCCGAACTCCTATC[C/T]CTGACTTCAGGGCCC	338692
rs760654629	snp	A/G	6.66189e-05	0.00577105	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301344	CTGTGTGGCTGTGAT[A/G]AGCCCCTGAGCTCCG	338692
rs760709545	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290846	AGGAGCAGGCTCGGA[C/G]GGAGCCACTGTGCCC	338692
rs760764075	snp	G/T	0.000166959	0.00913518	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302075	TTCTGCCCCAGCCTT[G/T]GCGCTCACTGGCCTG	338692
rs760844819	snp	C/T	6.61507e-05	0.00575074	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291490	GGCCCCCGATTTCTA[C/T]GTTGAGATGAAGTGG	338692
rs760852080	snp	G/T	1.66018e-05	0.00288108	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301034	AGCACCCGCTCTCCC[G/T]GGGTGACCAGGTGAC	338692
rs760857878	snp	C/T	4.98144e-05	0.00499047	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302184	CCCCTCCCAGGACAC[C/T]CCCAGCCCCCGGTCC	338692
rs761308283	snp	A/G	1.68255e-05	0.00290043	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301590	TCCGGGACGAGGACG[A/G]TGACCTCCTGCAGTT	338692
rs761338558	snp	A/G	1.66991e-05	0.00288951	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301520	GAGGTGGACCCCACC[A/G]TGTTTGAAGTGCCCA	338692
rs761426012	snp	A/G	1.8271e-05	0.00302244	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299869	TGGGGATGGCGCAGC[A/G]GCATTCCTCCCACAC	338692
rs761427954	snp	C/G	1.68088e-05	0.00289899	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301586	CCCCTCCGGGACGAG[C/G]ACGATGACCTCCTGC	338692
rs761460148	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67297502	GCCTGGCCTGGCCTT[C/T]ACCTGTGTCTCATAA	338692
rs761514301	snp	A/G	9.21583e-05	0.00678754	intron-variant	ANKRD13D	GRCh38.p7	11:67299939	GGGCCGAGCCTGGGC[A/G]GGAGGGCACCCTCTG	338692
rs761553794	snp	C/G			intron-variant	ANKRD13D	GRCh38.p7	11:67292570	ACCCTTCCAGCAAGA[C/G]TTTCTCTGACAACAC	338692
rs761605150	snp	A/G	1.65888e-05	0.00287996	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291731	GGCCGGAGGAGCTTC[A/G]TCTTCAAGGGCCAGG	338692
rs761671934	snp	A/G	1.65214e-05	0.0028741	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291669	GGGGTGAGAGCCTGC[A/G]AGTAGACACCAGTCT	338692
rs761722832	snp	C/T			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302835	AGGAAAAGCCTGGGT[C/T]CCCAGGCACCATTCA	338692
rs761730175	snp	C/T	0.000151252	0.00869499	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302194	GACACCCCCAGCCCC[C/T]GGTCCACCCAGCTTT	338692
rs761816425	snp	A/T	1.70603e-05	0.0029206	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302280	AGCGGCGCGGGCAGC[A/T]GGAGGAGGAGGACTT	338692
rs762003780	snp	G/T	7.36784e-05	0.00606908	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301849	CATGGGGCTGGCTGG[G/T]TCCCTGTCCCCCCAG	338692
rs762045994	snp	A/G	7.31609e-05	0.00604774	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290461	GGTACAGCAGGGCAC[A/G]GTTATGGAGGTGGGG	338692
rs762095591	snp	A/G	1.67281e-05	0.00289202	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301002	CAGGTTCAAGGCAAC[A/G]CTGTGGCTGAGTGAA	338692
rs762164354	snp	A/G/T	8.26173e-05	0.00642665	intron-variant	ANKRD13D	GRCh38.p7	11:67300918	AAGGCAGCTGCCCAC[A/G/T]AACCAGAGGGCAGTC	338692
rs762253329	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298300	ATCTCCTGACCTCAT[A/G]ATCCACCCCCCTTGG	338692
rs762258196	in-del	-/CCCA	1.82961e-05	0.00302452	intron-variant	ANKRD13D	GRCh38.p7	11:67299809	GACCCCTTACCAGCT[-/CCCA]CCCCTTCTCCGTAGC	338692
rs762319798	snp	A/G			intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299473	TTCTGCACTGGTGAG[A/G]CTGAGTGTGGGGAGC	338692
rs762434017	snp	A/G			upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302239	CCTGGCCCTGGAGTT[A/G]TCTTCACGGGAGCAG	338692
rs762455831	snp	C/T	1.69533e-05	0.00291142	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292161	ACCCACCTGGACACT[C/T]GTAATGTGGCCTTTG	338692
rs762558173	snp	C/G	1.66663e-05	0.00288667	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67292083	GAGCCCGAAACACTG[C/G]TGGCCGCCATGCGGC	338692
rs762572514	snp	A/C	3.36791e-05	0.00410346	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301429	GAAGAGGGAGCCTGC[A/C]CAGCTTTCTGGTCAC	338692
rs762662570	snp	A/G	1.67189e-05	0.00289122	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301505	AACCCTTTCCCGTGC[A/G]AGGTGGACCCCACCG	338692
rs762820762	snp	G/T	1.82627e-05	0.00302175	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299846	GAAGACTCCATTCCA[G/T]TCCTTCCTGGGGATG	338692
rs762848094	snp	A/G	3.30382e-05	0.00406423	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291659	GTGTGGAAGCGGGGT[A/G]AGAGCCTGCGAGTAG	338692
rs762877306	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67292520	GGTGCGGCTGTGTTG[G/T]GGGCAGAATCCTTTG	338692
rs762910949	snp	C/T	1.65291e-05	0.00287476	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291534	GGGGTGAGTGGGGAC[C/T]TCTGGGCTCCCAGGG	338692
rs762960172	snp	C/T	1.65261e-05	0.0028745	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299106	GAAGATGGAAACTGT[C/T]AGCGGCTACGAGGCC	338692
rs763003043	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293218	ACTGATAACTCATTG[G/T]TTAATTGACTGTTTA	338692
rs763067713	snp	G/T			intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301204	GCACCCTCCCTCAGC[G/T]CAGTCCCTGGAGAGC	338692
rs763121486	snp	C/T	0.00011552	0.00759913	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290102	GAACAGGAGGACCCC[C/T]GCGGGCGGACCCCAC	338692
rs763192835	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302585	CTGGGCTTGAATCCT[A/G]GTCATGGTCCCCTTA	338692
rs763213094	snp	A/G	7.78847e-05	0.00623989	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290359	TGGAGACCCCGAGAT[A/G]GTGCAGCTGGTGCTC	338692
rs763252423	snp	A/G	6.81779e-05	0.00583818	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301763	CCCTGACCAACACCC[A/G]GCCCGGTGCCCGCCC	338692
rs763312380	snp	C/T	7.08416e-05	0.00595112	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301675	TGCCCAGGGGGTGGG[C/T]TCTGGCCTCTGCAGC	338692
rs763526520	snp	C/G	1.66801e-05	0.00288787	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300164	CTTGCCTCGGGACAA[C/G]GGCTCTTGCAGACCC	338692
rs763617809	snp	C/G/T	3.41864e-05	0.00413428	intron-variant	ANKRD13D	GRCh38.p7	11:67300981	CATGTCCTGTGGTCG[C/G/T]CTGGGCAGGTTCAAG	338692
rs763617829	in-del	-/A	0.000110369	0.00742781	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299504	AGGCTCTGAGCCCCC[-/A]GCTCCCCGTGTCCCC	338692
rs763654189	snp	C/G	3.36882e-05	0.00410402	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301437	AGCCTGCACAGCTTT[C/G]TGGTCACCAAGCCCC	338692
rs763751492	snp	A/G	1.82633e-05	0.00302181	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299861	GTCCTTCCTGGGGAT[A/G]GCGCAGCAGCATTCC	338692
rs763835861	snp	C/T	1.65296e-05	0.00287481	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291541	GTGGGGACCTCTGGG[C/T]TCCCAGGGATTTGGG	338692
rs763853872	snp	C/T	0.000124758	0.00789706	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302104	TGTTCTTCCCTCCCC[C/T]GCCCTGCCTGGAAGG	338692
rs763902810	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291271	CTGAGGTGGAAGAAT[C/T]ACCTGAGCCCAGGGA	338692
rs764089865	snp	C/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67302711	GTCCTTACCAAGCAG[C/G]CGTCCTGTGAAAGTC	338692
rs764104705	snp	A/C	0.000101404	0.00711983	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302191	CAGGACACCCCCAGC[A/C]CCCGGTCCACCCAGC	338692
rs764189057	snp	C/T	1.65315e-05	0.00287498	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299109	GATGGAAACTGTTAG[C/T]GGCTACGAGGCCAAG	338692
rs764208135	snp	C/G	1.66421e-05	0.00288458	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290369	GAGATGGTGCAGCTG[C/G]TGCTCCAGTATCGGG	338692
rs764238756	snp	C/T	1.77628e-05	0.00298011	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301677	CCCAGGGGGTGGGCT[C/T]TGGCCTCTGCAGCCA	338692
rs764481783	snp	A/G	2.31179e-05	0.00339977	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301764	CCTGACCAACACCCG[A/G]CCCGGTGCCCGCCCT	338692
rs764513964	snp	A/C/G	4.95834e-05	0.00497892	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300063	AGTACTTCGACCCCA[A/C/G]CTTCAGCCTGGAGTC	338692
rs764693875	snp	G/T	1.81724e-05	0.00301428	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291992	CTACCGGCCGGCAGA[G/T]GCAGGAGCCCTGGTG	338692
rs764699545	in-del	-/CC	1.83122e-05	0.00302585	intron-variant	ANKRD13D	GRCh38.p7	11:67299796	ATGCGAGCATTGTGA[-/CC]CCTTACCAGCTCCCA	338692
rs764701952	in-del	-/CAAT			intron-variant	ANKRD13D	GRCh38.p7	11:67296399	TGTTGTTATATTTAC[-/CAAT]CAGTCTCTTGACTTG	338692
rs764729695	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295395	TCACTCCAGCCTGGG[C/T]GACAGACCAAGACTC	338692
rs764845999	snp	C/T	9.17238e-05	0.00677152	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291985	TCCACCCCTACCGGC[C/T]GGCAGAGGCAGGAGC	338692
rs764892198	snp	A/G	1.68241e-05	0.00290031	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301420	CAACGGGAGGAAGAG[A/G]GAGCCTGCACAGCTT	338692
rs764945916	snp	A/G	3.33211e-05	0.0040816	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301370	CTCCGTGTGGGTGCC[A/G]GCCCCCAGCTCTGCT	338692
rs764978869	snp	C/T	1.83397e-05	0.00302812	intron-variant	ANKRD13D	GRCh38.p7	11:67299779	GGAGGTGGGCAGGGG[C/T]GATGCGAGCATTGTG	338692
rs765073960	snp	A/G	0.000102886	0.00717164	missense, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299534	CTGCTCCCCAGGTGT[A/G]CAGTGCCACCAACGT	338692
rs765170445	snp	A/G	4.91461e-05	0.00495688	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301775	CCCGGCCCGGTGCCC[A/G]CCCTCCTCCCCAGGC	338692
rs765225368	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291183	GGCAACATGGTGAAA[C/G]CCGTCTCTACAAAAA	338692
rs765249711	snp	C/G	3.32088e-05	0.00407471	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291428	CTCCCAGGCCTGCTG[C/G]AGCCAGCAGCAGGCA	338692
rs765320673	snp	C/T	1.66704e-05	0.00288703	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301137	TCCACCTGGCTTCCC[C/T]GTCAAAATTGGTGAG	338692
rs765674940	in-del	-/TTTTTTTTTTTTTTTT			intron-variant	ANKRD13D	GRCh38.p7	11:67298057	TTTATTGAGGTTTTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTGAGACG	338692
rs765745556	snp	A/G/T	8.74033e-05	0.00661021	intron-variant	ANKRD13D	GRCh38.p7	11:67299975	TTGATGGCTGAGTCC[A/G/T]CCCTGGGACCCACGC	338692
rs765757097	snp	G/T	1.759e-05	0.00296558	intron-variant	ANKRD13D	GRCh38.p7	11:67299969	GTCACCTTGATGGCT[G/T]AGTCCGCCCTGGGAC	338692
rs765898896	snp	C/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293622	TCTAAGTAGCTGGGA[C/T]TACAGGTGCATGCTG	338692
rs765953329	snp	C/T	0.000132586	0.00814098	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67300039	ACCCCACAGCCATCT[C/T]CCCTGAGGAGTACTT	338692
rs765999208	snp	C/G	3.38713e-05	0.00411516	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291770	TGGACAAACTCATTG[C/G]AGCTCCTCGGCCCTT	338692
rs766016023	snp	A/T			intron-variant	ANKRD13D	GRCh38.p7	11:67295612	ATGGTGGTGGGCACC[A/T]GTAGTCCCAGCTGCT	338692
rs766072374	snp	C/T	3.51648e-05	0.00419299	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302316	GGATCCTGCAGCTGT[C/T]ACTCACTGAGCACTG	338692
rs766231995	snp	C/T	1.72249e-05	0.00293465	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301265	GCCAGGGCTCAGGCG[C/T]GGCTGTCTTCTCACA	338692
rs766320106	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290944	TGGCCAGGTTGAGGC[C/T]GGCCCTCCACCTCCA	338692
rs766323529	snp	C/G	1.65523e-05	0.00287678	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	ANKRD13D	GRCh38.p7	11:67299121	TAGCGGCTACGAGGC[C/G]AAGGCAGGAGAGGCT	338692
rs766323738	snp	C/T	1.66571e-05	0.00288587	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301348	GTGGCTGTGATGAGC[C/T]CCTGAGCTCCGTGTG	338692
rs766404513	snp	C/T	0.000167827	0.00915891	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302077	CTGCCCCAGCCTTGG[C/T]GCTCACTGGCCTGTT	338692
rs766411442	snp	A/C	0.000111713	0.00747289	intron-variant, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299499	GGAGCAGGCTCTGAG[A/C]CCCCAGCTCCCCGTG	338692
rs766494766	snp	C/T	1.65811e-05	0.00287929	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301049	TGGGTGACCAGGTGA[C/T]CCCCATCATCGACCT	338692
rs766503232	in-del	-/T	1.67621e-05	0.00289495	upstream-variant-2KB, frameshift-variant, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301495	CTGCCTAGGGAACCC[-/T]TTCCCGTGCGAGGTG	338692
rs766510966	snp	A/C	1.65277e-05	0.00287464	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291507	TTGAGATGAAGTGGG[A/C]GTTCACCAGCTGGGG	338692
rs766582929	snp	A/G	1.65908e-05	0.00288012	synonymous-codon, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67301116	CGACTTCATCACTCT[A/G]CGCCTTCCACCTGGC	338692
rs766706645	snp	C/G	5.21046e-05	0.00510388	intron-variant	ANKRD13D	GRCh38.p7	11:67292189	TTGAGAGGTCGGTCG[C/G]GTCCTGGCACACCGT	338692
rs766750071	snp	A/G			intron-variant	ANKRD13D	GRCh38.p7	11:67298710	TTCCTTACCTTTTTT[A/G]AAAATGTTTCCTAGA	338692
rs766798037	snp	C/T	1.68284e-05	0.00290067	upstream-variant-2KB, synonymous-codon, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301591	CCGGGACGAGGACGA[C/T]GACCTCCTGCAGTTC	338692
rs766822754	snp	A/G	5.01375e-05	0.00500662	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301547	CCCAACGGGTACAGC[A/G]TGCTGGGCATGGAGC	338692
rs766875775	snp	C/T	1.91108e-05	0.00309112	intron-variant	ANKRD13D	GRCh38.p7	11:67299649	GCTGCCCGGTCACAC[C/T]GTGTGGTGGGGTCAC	338692
rs766901320	snp	A/G	1.66946e-05	0.00288912	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301529	CCCACCGTGTTTGAA[A/G]TGCCCAACGGGTACA	338692
rs767040226	in-del	-/TTA			upstream-variant-2KB, cds-indel, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302384	GCCCGCTTTTGTAAT[-/TTA]TTTATTTATAAACTC	338692
rs767067045	snp	C/G	1.82774e-05	0.00302297	missense, nc-transcript-variant	ANKRD13D	GRCh38.p7	11:67299871	GGGATGGCGCAGCAG[C/G]ATTCCTCCCACACCG	338692
rs767099014	snp	A/G	1.68111e-05	0.00289918	upstream-variant-2KB, missense, nc-transcript-variant, downstream-variant-500B	SSH3, ANKRD13D	GRCh38.p7	11:67301587	CCCTCCGGGACGAGG[A/G]CGATGACCTCCTGCA	338692
rs767241002	snp	C/T	3.30508e-05	0.00406501	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67291679	CCTGCGAGTAGACAC[C/T]AGTCTCCTGGGCTTC	338692
rs767268826	snp	G/T			intron-variant	ANKRD13D	GRCh38.p7	11:67293491	ATCCTTTACTCATTT[G/T]TTATTTAACTTAATT	338692
rs767277128	snp	C/T	3.35576e-05	0.00409606	intron-variant, downstream-variant-500B	ANKRD13D	GRCh38.p7	11:67301156	AAAATTGGTGAGAGG[C/T]TGGGCACAGGCAGCG	338692
rs767386730	snp	C/G	5.07318e-05	0.0050362	upstream-variant-2KB, missense, nc-transcript-variant	SSH3, ANKRD13D	GRCh38.p7	11:67302195	ACACCCCCAGCCCCC[C/G]GTCCACCCAGCTTTG	338692
rs767522384	snp	C/T	7.50103e-05	0.00612369	intron-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290463	TACAGCAGGGCACAG[C/T]TATGGAGGTGGGGTA	338692
rs767522831	snp	C/T			upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67288388	TAGGGAAAGGGAGAA[C/T]AGAGGGTCAGCCTTG	338692
rs767575142	snp	C/T	1.65842e-05	0.00287955	missense, nc-transcript-variant, upstream-variant-2KB	ANKRD13D	GRCh38.p7	11:67290400	ACTACCAGAGGGCCA[C/T]GCAGAGGCTGGCGGG	338692
rs767634941	snp	C/T	4.02868e-05	0.00448796	intron-variant	ANKRD13D	GRCh38.p7	11:67300933	GAACCAGAGGGCAGT[C/T]CTCAATGGAAGGGCC	338692
rs767648033	snp	A/G	1.87862e-05	0.00306476	intron-variant	ANKRD13D	GRCh38.p7	11:67299652	GCCCGGTCACACCGT[A/G]TGGTGGGGTCACCCT	338692
rs767727494	snp	C/T	8.44987e-05	0.0064994	upstream-variant-2KB, intron-variant	SSH3, ANKRD13D	GRCh38.p7	11:67301858	GGCTGGGTCCCTGTC[C/T]CCCCAGCCCTGGCTT	338692
rs767731264	in-del	-/AG	1.84578e-05	0.00303786	intron-variant	ANKRD13D	GRCh38.p7	11:67299912	GGGCTGGGCCGAGAC[-/AG]GGCTGGCGGGGGGCC	338692

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