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

ANKRD13A

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs548987327	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026118	AAGCACCCACCACCA[C/T]GCCCGGCTAATTTTT	88455
rs549003313	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110024773	CACTTGTCATAGTGC[C/T]GAGTGTGTTTTCTGC	88455
rs549003477	snp	A/G	0.000256513	0.0113221	intron-variant	ANKRD13A	GRCh38.p7	12:110033749	TTGCAAAAAGTTGGA[A/G]TGGAAATGTAATGAA	88455
rs549145909	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110001409	CCCTCACCGAAGTCC[A/G]AAATTACCCTCTTTT	88455
rs549152701	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010434	AGTTCATAAGTTCAT[C/T]GTCTTGTTACTTTTA	88455
rs549172528	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035613	CACCACCAGACCCAG[A/C]TAGTTTTTGTGTTTT	88455
rs549235803	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110026922	TTCCTTAGTCTGACT[C/T]ATTCTTGGAGGTGTT	88455
rs549263134	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025574	TGCATTTTTCAGTTG[A/T]TAGTTTATATACTTT	88455
rs549555271	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035951	TGGTCACTTGAACTT[C/T]GCCCAAGGTCAGCTG	88455
rs549646488	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015727	AATTTTTGTATTTAT[A/G]GTGGAGATGGGGTTT	88455
rs549648854	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110022292	ATATCTACTAAAAAT[A/G]TAAAAAATTAGCCAG	88455
rs549796848	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016639	CCGGTCTTCCCCGCC[A/G]TGCATAGGACTTTTC	88455
rs549811295	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027160	ACATCCCAGCCCCAT[C/T]CCAGCCCCACCAGTT	88455
rs549832374	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001974	GTTTTTAGGAATCTA[A/C]TTCTTTTGGTGCCCA	88455
rs549997034	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033221	CCACGCCCGGCTAAT[-/T]TTTTTTTTTTTTTTG	88455
rs550028830	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110019978	GCCTTTGAGTAGAGG[C/T]TGTCAAAGCTGTTCG	88455
rs550067175	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110009498	TCTATCTAACTAAAT[A/G]TTCGTCAATGTTGTT	88455
rs550121282	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037652	GGGCCTGCACCTTGC[A/G]TGCATGCAGCAGGCA	88455
rs550130607	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001461	TTTTTTCTTTTTGAG[A/G]TGGAGTCTCGCTCTG	88455
rs550186276	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110005973	AGGTGTGCACCACCA[C/T]GCCTGGCTAATTTTT	88455
rs550330553	snp	A/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110007612	CTCGAACTCCCGACC[A/T]CAGGTGATCCGCCCA	88455
rs550511716	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006985	GAATTATTTTGGCAC[A/C]CTTGTTGAAAATCAA	88455
rs550586148	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999493	CGGGGTGGGCGCGGC[A/C]GACCTGGTCCCTGAG	88455
rs550691267	snp	A/T	0.00676609	0.0577691	intron-variant	ANKRD13A	GRCh38.p7	12:110024411	TTCCCTTAATTATTT[A/T]AAAAAAAAAAAGGAA	88455
rs550693561	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014543	CTGTAAATGACCTGC[A/G]TACTTAGTGGCTCCA	88455
rs550707917	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110016243	ATGAGCCACCTCACC[C/T]GGCTAGGGGCTTACA	88455
rs550779429	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005955	CCTAGTAGCTGGGAT[C/T]ACAGGTGTGCACCAC	88455
rs550792743	snp	A/G	0.00597247	0.0543191	intron-variant	ANKRD13A	GRCh38.p7	12:110033211	GGTGCCCGCCACCAC[A/G]CCCGGCTAATTTTTT	88455
rs550867049	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032079	TACTGGACTGGCTAG[A/G]ACATCTAGTACAATG	88455
rs550901164	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000074	GCTACGTGCCTTGTG[C/T]GAGGCCGCCCCGCTG	88455
rs550997673	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039069	TCACAATCTGTTTTG[G/T]TTTTTTTTTTTGTCA	88455
rs551009249	snp	A/G			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998777	ACGATTTTTCTCCCC[A/G]AGACGACATTTGGCA	88455
rs551118663	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035436	ATAGTGAGATCCTAT[A/G]TCTACCAAATTTTTT	88455
rs551166522	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022426	TGCACTCCAGCCTGG[C/G]TGACAGTGTAAGAGT	88455
rs551216042	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029796	TGTGGTTTGATTTAA[A/G]GAAGTGTTATGATTA	88455
rs551309164	snp	A/C	0.00119737	0.0244387	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999557	GCACCCGACCGGCTC[A/C]GCCGGCCGGCAGCGT	88455
rs551346844	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008637	TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA	88455
rs551489679	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007716	AAACAATGTTTTATG[G/T]TTTAAGAGTATGTAA	88455
rs551577101	snp	A/G	1.64779e-05	0.00287031	missense, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033884	ATGGCAGAAATGTGC[A/G]TTTGCAAGATGAAGA	88455
rs551642765	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034676	AGTCCAAGGCTTGAG[A/G]TCCTCCTCCCCTAAC	88455
rs551645577	in-del	-/G	0.00240384	0.0345853	intron-variant	ANKRD13A	GRCh38.p7	12:110023958	CACTAACTTAAGCTG[-/G]GGGGGGAAAAAAACT	88455
rs551791653	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032824	AAGCATAATGTTGAA[C/T]GAAGAAAATCCAATT	88455
rs551915629	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022317	AGCCAGACGTGGTGG[C/G]GGGCGCCTGTAGTCC	88455
rs551937855	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110009239	GGCATGTGCCACCAC[A/G]CGCGGCTAATTTTGT	88455
rs551968096	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110006862	TGGCCTCCCAAAGTG[C/T]TGGGATTATAGGGAT	88455
rs551979518	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023424	GAATTAACAGCTGGG[C/T]TAAAAAAATCTGTTT	88455
rs552029456	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015514	AGGTTTGACTTTTAT[C/T]CCCCTCCAATCCTCT	88455
rs552107990	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110009270	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	88455
rs552255806	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030090	AGTATTAATTTTGGA[C/T]AGTTGTATGTTCATG	88455
rs552361037	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997365	GCCTGGGGGACAGAG[C/T]GAGACTGTCTCAAAA	88455
rs552509628	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005673	AATTCCTTTTTATCA[C/T]TGAATATATTCCATT	88455
rs552563827	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110004168	ATCTCAAAAAAAAAA[A/T]AAATTTTTTTTAAGG	88455
rs552586772	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110002808	TCCTGTTCCAGGAAC[A/G]GCAACACAAGAAAGA	88455
rs552647010	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004629	AGAGGGAGACTCTGT[C/G]TCAAAAGAAAAAGTG	88455
rs552695052	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020417	TAAGTATCCTTTTCT[C/T]CTAATTTAGATTGAG	88455
rs552783068	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037789	AGGCTAAGGGGAGGA[C/G]AGCATCATCACTTTC	88455
rs552788550	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012917	GGTCGGGAGAGGTGG[A/C]CGGGGTTTGATCAAG	88455
rs552830538	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997555	ATTTTTAAAGGGTTG[C/T]GAGATGAAAATGAAG	88455
rs552844382	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038477	TTTCCACGTAGACAC[C/T]TAGGAAGAGCCCGCA	88455
rs552869740	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038744	TTTCTCAGGCCTTTT[G/T]TGGATACCTTTAGTA	88455
rs553233383	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024848	CTTTGTTAACTGTTA[C/T]GTTTGATTTTCTAGA	88455
rs553326223	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110022085	GTTACCAAGGGCCAC[A/T]GAGTTATTAGGAAAT	88455
rs553387536	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036907	AACGTACTGAGTCAG[C/T]TTTTTCTGATTGGTT	88455
rs553453027	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028559	CCCCACAGCCATCAC[A/G]CCTGATGAGTACTTC	88455
rs553461574	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110017964	GCATACTTTAGACAT[C/T]TGATACTCTGAATGG	88455
rs553462321	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110036083	GTGGCATGTTACTAC[C/G]TCCCACTTAGGTGTT	88455
rs553564214	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012358	GCAATAGAGCAAGAA[A/C]TTTTCTCAAAAAAAA	88455
rs553679304	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004082	AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG	88455
rs553715358	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029097	TGAAAGCTAACAGTA[A/G]ATTGTCCATGTTATT	88455
rs553716623	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008874	TGGGCGACAGAGCGA[A/G]ACTCAGTCTGGAAAA	88455
rs553975089	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011373	GGATGGAAGTGACGC[A/G]TGTGCACTTGCCTAT	88455
rs554038479	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003473	ACTGGCCTCAAGATT[C/G]CTGTTTCCACTGACT	88455
rs554240733	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110010876	CTGCAGGGGTAGTTA[A/G]TACCTGAATAACAGC	88455
rs554251339	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028272	TTTTCTTTGTTATAA[C/T]CAGGAGATAAAAATG	88455
rs554587006	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011414	GTAGATCCGCATACG[C/T]GCCCGGCAGATCATG	88455
rs554642074	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001095	CCCAACAATTCTGGG[A/G]GGTATTGGTGCCCTC	88455
rs554848714	snp	C/G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003606	GGAGTCCCCCTAAAG[C/G/T]TGACAGTGAGTTTAT	88455
rs554901798	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009684	TTCAGATGAGAGAGA[C/T]GCAGGAAGGTCTGAA	88455
rs554983784	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110035247	GTTGACCATAAGTTT[C/T]AACAAGGGAAGTAGC	88455
rs555041522	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009632	AAAATCACACTGTCA[C/T]CATAATACAATTACA	88455
rs555126031	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036167	TGGTCATGGAAAGAC[C/T]TTTAATTTGGTTCTT	88455
rs555240024	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016783	TTTATTTTTATTTTT[A/G]TTTTTTTGAGACAGA	88455
rs555317303	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110023868	AACTGTGGGAGGAGG[G/T]TGGAGGGTGCATAAG	88455
rs555365502	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025005	TAGAGAACCTTGTGT[C/T]CATACCTTTCTCTTC	88455
rs555386011	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033375	CAGTTATTGATAGTG[G/T]TCTGTGTCTTAGGCT	88455
rs555447164	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110025173	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	88455
rs555447499	snp	C/T	5.30209e-05	0.00514856	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033981	ATCAGAATACTCTAA[C/T]GGCAGGGCGTGGGAG	88455
rs555452346	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032395	TAAATTAAGACTTCA[A/G]ATAAAAACAATTGAA	88455
rs555510868	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110015056	GCTGGGATTACAGGC[A/G]TGAGCCAGTGCGCCC	88455
rs555707718	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026040	GACCTTGGCTCACTG[A/C]AACCTCTGCCTCCTG	88455
rs555814676	in-del	-/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110005950	GCCTCCCTAGTAGCT[-/G]GGATTACAGGTGTGC	88455
rs555956973	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998748	GTTCAAATAGAAGCG[C/G]TTCTCAACTGAGGAC	88455
rs556002491	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034119	TGGTCTTCTTACAAA[A/C]GCTTGTTATGTAAGA	88455
rs556014672	snp	A/C	0.00478085	0.0486577	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999631	GGCGGGCGCGGGAGA[A/C]CCCGCCGGGGCCGAG	88455
rs556103503	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015798	CTCATCCACCCGCCT[C/T]GGCCTCCCAAAATGC	88455
rs556110822	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001686	CTACCTCCCAAAGTG[C/T]TGGGATTACAGGCAT	88455
rs556167321	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026489	GGCTGAGGCAGGAGA[A/C]TCACTTGAACCTGGC	88455
rs556231309	snp	C/T	0.000404394	0.0142139	intron-variant	ANKRD13A	GRCh38.p7	12:110021137	TCAAGCTAACTCTTT[C/T]GCAACTGACAGTGTG	88455
rs556241913	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017343	TATTGGAATAGCTTA[-/T]TTTTTTTTTAACAAA	88455
rs556309466	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110008029	AGAATCTCTAGTACA[A/G]TGTTGACTAGATATG	88455
rs556361467	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018712	CAGTTACCCTTGTGA[C/T]GTGTCTGCTTCACTT	88455
rs556499195	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003507	CGTGGGGGCCACACA[A/G]GACCAGGATGGTCTG	88455
rs556501295	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997651	CAAAGTTAAACATTC[A/G]TTTTGGCTAAGGACA	88455
rs556635486	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035924	TGTCTCTAAAAAAAC[A/G]AAAACCTGCTTTGGT	88455
rs556720607	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036361	CTCTGGAATAAACCA[C/G]GGTGAACACAGGCCT	88455
rs556777823	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006342	GTTGTTTTGTTTGTA[C/T]GCATCCTAGTGGGTG	88455
rs557061329	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038647	GGATAAATCTATTTT[C/T]TAACAATCTTTTTAT	88455
rs557174365	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039375	AGTGTTTTTCATATA[C/T]GTGTTCACTCTAAAA	88455
rs557241626	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110031529	CTGATTTTTGTATTT[C/T]TATTAGAGACTGGGT	88455
rs557432508	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021093	AAGGCACATTTTGTA[C/T]TTTTGTGCCCACAGG	88455
rs557436579	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030387	GGTTAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	88455
rs557446047	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038018	TGTTCACCAAAGAAA[C/T]GGGTAATCTGTGCTG	88455
rs557623933	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013783	TGACAGAGCAAGACC[G/T]AAAATAATAATAAAT	88455
rs557709056	snp	C/T	0.00438332	0.0466095	intron-variant	ANKRD13A	GRCh38.p7	12:110015957	GTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTCCAT	88455
rs558093140	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012228	AAATTAGCCAGGTGC[G/T]GTGGTGCATGTCTGT	88455
rs558098812	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033353	AGGCGTGAGCCACCG[C/T]GCCCGGCAGTTATTG	88455
rs558247480	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030434	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGTGTA	88455
rs558351763	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006475	AGAAATGTCATCTCA[A/C]ATCCTTTGCCCATTT	88455
rs558351778	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014845	CTGGAGTGCAGTGGC[A/G]CGATCTTGGTTCACT	88455
rs558420525	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007082	CTTATGCCAGTACCA[C/T]GTTGTCTTGATTGCT	88455
rs558494002	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013817	ATAATATAATAATAA[A/G]TGATAATAAAGTAAA	88455
rs558560382	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005509	CCAACCCCTCCAGCC[C/T]AGGCAACCTGCTAAC	88455
rs558676021	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110006937	ATGCAGTTGTTCAAG[C/T]GGCACTTGTTGAAAG	88455
rs558697071	snp	A/T	0.0103295	0.0711199	intron-variant	ANKRD13A	GRCh38.p7	12:110026421	TGTGCTAAAAAAAAA[A/T]ACAAAATTAGCTGGG	88455
rs558741683	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034944	GAGAACAGTGCTCAC[A/G]CTCCAGCGTCCTCAC	88455
rs558885799	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038346	GGCAGCTAATCCTGT[C/T]CCTGAAGGAGCAGCT	88455
rs558999305	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002455	AACCCCGTCTCTACT[A/T]AAAATACAAAAATAG	88455
rs559083903	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028439	CACGTCCACCTCAGA[C/T]ACTGAGTGCCACAGG	88455
rs559102605	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029307	GCCAGATTTTAGGGT[G/T]ATGTGAATTCCTTGT	88455
rs559105279	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030489	CACAACTCTCAATCT[C/G]AGTTTTCCCGTCTGT	88455
rs559217310	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036769	AAAAAAAAGACTAAA[G/T]TGTTGGCTCTCTTGC	88455
rs559226409	snp	C/T			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997992	GTTAGCCAGGTACTA[C/T]TTTGGTTTTAGATAC	88455
rs559242747	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029698	TGTGGGTGGCAGCAT[G/T]TGGGTGGCAGGATGC	88455
rs559435860	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015954	TTGTTTTTTCTTTCT[-/T]TTTTTTTTTTTTTTC	88455
rs559453755	in-del	-/CT	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110015904	CAAGGTAAAATAACA[-/CT]CTAATATTTAATAAA	88455
rs559490263	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003066	GTGTTCTGCTTATGT[C/T]GTTGGCCGCTTAGCT	88455
rs559611891	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026804	GGAGAATCGCTTGAA[C/G]CCCAGAGGTGGAGGT	88455
rs559633749	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110002632	AAAAACAAAAAAAAC[C/T]CAAAAAATTCTTATC	88455
rs559740004	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029032	TGAGCCACTGCGCCC[A/G]GCCTCCTCTGCCCCT	88455
rs559807874	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020246	CCAGCTCTCTGCAAG[C/T]CTAAGTAGCTTACCC	88455
rs560091455	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023232	CCTGTGAGAGGGAGC[A/G]TTTCCCAGGGCAAGC	88455
rs560204521	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110017002	TGGTCTCAAACTCCT[A/G]ACCTCAGGTGATCCA	88455
rs560224302	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010118	GTGATCCACCCACCT[C/T]GGCCTCCCGAAGTGC	88455
rs560301628	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034208	TTTTCCTCATATTCA[C/T]GCACATAGCTTGTAA	88455
rs560435288	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033691	AGTAAGCCTTGATTG[C/T]TATAATTTTGAGCCT	88455
rs560464580	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001724	TGTTGCCGGCCTTTT[A/T]TCATTTAAAAAGAAT	88455
rs560571048	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016331	CTGTTAACCCCTGCT[A/T]ATGTTGTGTTGATAG	88455
rs560714865	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036945	CTATGAATGATGTAT[A/G]ATCACAGGGCCTAGA	88455
rs560757332	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110002721	GTCAGTTTCCTCATT[C/T]CGTCTATCACCTGAT	88455
rs560785686	snp	C/T	0.00755907	0.0610114	intron-variant	ANKRD13A	GRCh38.p7	12:110026134	GCCCGGCTAATTTTT[C/T]GTATTTTCAGTAGAG	88455
rs560886927	in-del	-/T	0.00372298	0.042984	intron-variant	ANKRD13A	GRCh38.p7	12:110036342	GGTGATTGACTGACG[-/T]TGACTCTGGAATAAA	88455
rs560912244	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001898	TTTTCTATTACTAGA[C/T]ATGGTACAGAGGTAA	88455
rs561020469	in-del	-/TGTTTGTTTGTT	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110019770	TACTATATAGTTAAA[-/TGTTTGTTTGTT]TGTTTGTTTGTTTGT	88455
rs561047872	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110010138	TCCCGAAGTGCTGGG[A/T]TTACAGGCATGAGCC	88455
rs561262526	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026182	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACATCA	88455
rs561301910	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017130	GGCCAGGCTGGTCTC[A/G]AACTCCTGTCCTCAG	88455
rs561589495	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038988	TCCAGGTAACGTCTG[A/T]ATCATACAGTTAGTG	88455
rs561650928	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110024201	TTTTTTCATGCATCT[A/G]TGCCATGGAGATGCT	88455
rs561772230	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021951	TTGTGTAGCAACCAC[C/T]AAGACACAGTGCCTG	88455
rs561895237	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110008449	ATAAGAGATATTAGT[A/G]TGTGGTTTTCTTTTC	88455
rs561909803	snp	A/G	0.00557542	0.0525036	intron-variant	ANKRD13A	GRCh38.p7	12:110014269	TACAAAAAATTAGCC[A/G]GGTGTGGTGGCGGGC	88455
rs562037426	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005920	CTCCTGGGTTTAAGC[A/G]ATTCTCCTGTCTCAG	88455
rs562097298	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006682	GCTTACCACAACCTC[C/T]GCCTCCCAGGTTCAA	88455
rs562439462	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018651	CTCCATCCCTGTCTT[C/T]GTTCTTGTCTGGCTA	88455
rs562443254	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110016227	TGCTGGGATTACTGG[C/T]ATGAGCCACCTCACC	88455
rs562555691	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033606	TGTTTCCACTAAAAT[A/C]AAGGAAAAAGAAAAA	88455
rs562581445	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015846	GTGAGCCACTGTGCC[C/T]GGCCATCTGTTCACT	88455
rs562642123	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000098	CCCGCTGATAAATGC[C/T]AAGTCGGGATTTTAA	88455
rs562770604	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009146	GAGTGCAATGGCACA[A/G]TCTCGGCTCACCACA	88455
rs562842765	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110006816	GATCAGGCTGATCTC[A/G]AACTCCCTACCTCAG	88455
rs562936213	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110005734	CGAAAATGTTTCTCC[C/G]TTTGTCAGTTGATGG	88455
rs563073683	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008121	ATTAACTATGATGTT[A/C]GTTGTGGGTTTTTTA	88455
rs563119254	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013356	AAGAGTTTTCTGATT[C/T]GTGAATATGAAATAC	88455
rs563182614	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014232	CCTGACTAACACGGT[A/G]AAACCCCATCTCTAC	88455
rs563243240	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110025993	TTGAGGCAAAGTCTC[C/G]CCCTGTCACCCAGGC	88455
rs563259297	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110022261	GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC	88455
rs563287972	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029868	TCATTTCTATTTGCA[A/G]ATGGTGCTGACAGAT	88455
rs563315114	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110031927	GTTTATCTTGTAACA[A/T]GGCTGAATTTACTTG	88455
rs563383443	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022502	TAGAGGCAGGATTGC[C/T]GAAGGAGCAGAGGTA	88455
rs563391382	snp	C/T	6.72857e-05	0.00579986	intron-variant	ANKRD13A	GRCh38.p7	12:110030627	TTTACTTATAAAAGT[C/T]TTTATTTTGTTTGTT	88455
rs563534710	snp	A/G			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997366	CCTGGGGGACAGAGC[A/G]AGACTGTCTCAAAAA	88455
rs563559036	in-del	-/TG	0.0193772	0.0965046	intron-variant	ANKRD13A	GRCh38.p7	12:110034443	GTAAGCAGTAGGCTT[-/TG]TGTGTGTGTGTGTGT	88455
rs563621605	in-del	-/T	0.0476504	0.146815	intron-variant	ANKRD13A	GRCh38.p7	12:110016282	TTCTTATTTTCTCTT[-/T]TTTTTTTTTTTTAAC	88455
rs563652059	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020359	CTTTTCTTTCTAGTA[A/T]AAAATTGGTTAATAA	88455
rs563740912	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110011664	TGTTCAGTGTTGTCC[A/G]GTGATTGCATTTCAT	88455
rs563789146	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028777	GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAGTGC	88455
rs563789432	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110019751	GGTCAGTCAGATTCA[C/T]ACTTACTATATAGTT	88455
rs563911427	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110031664	GACAAATGTATGCAT[C/T]TGTGTAACCACCACC	88455
rs563972820	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023054	TGCTAATAACCGCAT[A/G]TGTTCTTTGTAACGT	88455
rs564049195	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014299	CGCCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA	88455
rs564230060	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030799	TTAGTTTTGTTATTT[A/T]AAAAAAAATTTATGG	88455
rs564338881	snp	C/G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025093	GGGTGCAGTGGCTCA[C/G/T]GCCTGTAATCCCAGC	88455
rs564377050	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029408	TGTTGTCTAGCCTAC[C/T]GCATAGCAATAATCT	88455
rs564453024	snp	A/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110012590	AAACTTCTTCCACCA[A/T]ACACGAATGTGGAGG	88455
rs564585595	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110037139	TCCAAGTTCAATTCC[C/T]AGCCCTATCACTTAC	88455
rs564588317	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110011697	AAGCTCCTGGCCTTA[A/T]TTAGACTTAATTTGA	88455
rs564678253	in-del	-/AC	0.00119737	0.0244387	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038994	TAACGTCTGTATCAT[-/AC]AGTTAGTGTTGCCAG	88455
rs564727362	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038121	ATTCCTTCCACACCC[A/G]GCTAAAGTTAGAGGA	88455
rs564775207	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005868	GTTGCCCAGGCTGGA[A/G]TGCAGTGGCATGATC	88455
rs564798797	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036531	GAGGCAGGCGGATCA[C/T]GAGGTCAGAAGATTG	88455
rs565037528	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010171	CGCGCCTGGCTGAGT[G/T]TGAGTGTTAATCCTT	88455
rs565080490	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110028824	CTCACTGCAACCTCT[A/G]CCTCCCAGGTTCAAG	88455
rs565117811	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010357	AGTTTATGTAATAGA[A/C]GTGTAGGAAGATAAT	88455
rs565125136	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026265	CCACCGTGCCTGGCC[C/T]CTAACTTCTTTTTTA	88455
rs565182579	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011001	TCCCAGCTACTAGGG[A/T]GGCTGATATGGGAGG	88455
rs565247205	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029305	TTGCCAGATTTTAGG[A/G]TGATGTGAATTCCTT	88455
rs565252794	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033388	TGTTCTGTGTCTTAG[G/T]CTAGGTGAAGGGCAC	88455
rs565261357	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034530	CACCCTCAAACTCCT[G/T]GGTTCAAGAGATCCT	88455
rs565333465	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028113	TTGATGCTCACAGTA[A/T]CTATATGAACTTGGT	88455
rs565452496	snp	C/T	0.000132238	0.00813028	intron-variant	ANKRD13A	GRCh38.p7	12:110027778	AGGGGTAAGTTGAAG[C/T]AATGAGCTTTCATTG	88455
rs565596933	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028883	GCTGGGACTACAGGC[A/G]CGTGCCACCACGCCC	88455
rs565723093	snp	A/G	1.6554e-05	0.00287693	intron-variant	ANKRD13A	GRCh38.p7	12:110011975	AATGTAATACATCCA[A/G]TTATGTAAATGCCAG	88455
rs565723639	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009537	CCAAGAACCAACTTT[C/T]GGTTTTGTTGATTTT	88455
rs565784925	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001575	CTCCTCAGTAGCTGG[A/G]ATTACAGGCTAATTT	88455
rs565856257	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020670	CCGCATACCCTTCTG[C/T]AGACAGGGAGGCCCC	88455
rs565924374	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020075	ATGTCACATCCAGCT[C/T]TCTGCAAGCCAAAGT	88455
rs565988614	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011380	AGTGACGCATGTGCA[C/T]TTGCCTATTTCTTTG	88455
rs566043443	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002338	AAAAATTCTTAAGTC[C/T]GGGCACGGTGGCTCA	88455
rs566121592	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110026348	GGAGGCCAATGTGGG[C/T]GAGTCACCTGAGGTC	88455
rs566180952	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023344	ACTGAGATTTTGGGC[A/G]TATTACCAATGCTGC	88455
rs566578863	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008672	GGCAGATCACATGAG[A/G]TTAGGAGTTCAAGAC	88455
rs566580874	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999614	CGGCCTCAGGGCAGG[C/T]AGGCGGGCGCGGGAG	88455
rs566597629	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039130	GGCCAGTATAGGCAA[C/T]GTCACATTTGTTTGT	88455
rs566641479	snp	A/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038101	TCCTCCATCTATCTG[A/T]TTCCATTCCTTCCAC	88455
rs566668509	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034682	AGGCTTGAGGTCCTC[A/C]TCCCCTAACATCAAC	88455
rs566760207	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025592	GTTTATATACTTTCT[C/T]TGAAGGATCCTAATG	88455
rs566902501	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006006	ATTTTTAGTAGAGAT[C/G]GGGTTTCACCATGTT	88455
rs566978003	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036007	CTTCCACGTGGGTTA[C/G]CTGTATTTAAGAGAC	88455
rs567035920	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110015523	TTTTATCCCCCTCCA[A/G]TCCTCTTATTCTCTT	88455
rs567040715	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037725	CCTGGGCCCATCCAG[A/G]CTGCTCCCTGGGGTG	88455
rs567040753	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003851	AATATAGTAAGACTC[C/T]GTCTCCTTAAAAAAA	88455
rs567061203	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035082	ACCCATTCAGTTTTC[C/T]GAGCCAGACCCCAAA	88455
rs567115421	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007767	TATTTATTCCTAAAT[A/G]TTTTATTTTTTGATG	88455
rs567178334	snp	C/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110024663	ACAGGGATTGATGGC[C/T]TTTGGTGTTGGAGCC	88455
rs567379729	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110001446	TGTTTCTTTTTTTTT[C/T]TTTTTCTTTTTGAGA	88455
rs567390387	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032499	AGCTAAGGAACACTC[A/G]TGCACTCTTGGCTGG	88455
rs567461510	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017825	TAATCCCAGCTACTC[A/G]GGAAGCTAAGGCAGG	88455
rs567477336	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110035647	TAGAGACGGGGTTTT[A/C]CCATGTTGTCCAGGC	88455
rs567574917	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025590	TAGTTTATATACTTT[C/G]TCTGAAGGATCCTAA	88455
rs567595897	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026405	ATGGAGAAACCCCAT[C/G]TGTGCTAAAAAAAAA	88455
rs567635714	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003203	ACCTGGGTTGTGTGA[A/G]GTGGAGGGTGGCAAA	88455
rs567642636	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019708	AGGTTAGAATTGACC[C/T]AGTACTGAGTTCAGT	88455
rs567765051	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997595	AGGGAAATAAAGAAA[A/G]AGAGGAAGAAGAATA	88455
rs567879066	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007910	ATTTAATAGTTCTAA[C/T]AGTTTTTTGGTGGAT	88455
rs567896455	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999525	CGGCCGGCGACCCCG[G/T]ACCTCCCGCGCGCCC	88455
rs567949204	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110006221	TGTTTTAACTTTTTG[C/T]GGAACTGCCAGCAAT	88455
rs567964826	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016625	TGGGTGTTTTTCATC[C/T]GGTCTTCCCCGCCAT	88455
rs567990605	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033299	GATCTCCTGACCTTG[G/T]GATCTGCCTGCCTCA	88455
rs568025727	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998303	TGGTTTAACAACTCA[C/T]AAATCTTCTGGGCTC	88455
rs568033567	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014373	GCCGAGATTGCACCA[C/T]TGCACTCCAGCCTGG	88455
rs568085288	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013724	TGCAGTGAGCCACCC[C/T]TGAGTGAGGGTGCAG	88455
rs568627535	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038553	GGGAGCTGAAAACCA[C/T]GGAGCTCCATGGCTC	88455
rs568737917	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998530	TAGCTGTAAGTTGAT[G/T]TGGTTCTTCATTGAG	88455
rs568877117	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999503	GCGGCCGACCTGGTC[C/T]CTGAGCCGGCCGGCG	88455
rs568928015	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014657	TGTCTTTGCTCATCA[C/T]TGGAATGCTGGCAGA	88455
rs568956439	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033258	TAGTAGAGACGGGGT[G/T]TCACCATGTTAGCCA	88455
rs568997229	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012686	TAAATTGTGGCTAAA[A/G]GTAGCCTCTTCCTGG	88455
rs569158737	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039070	CACAATCTGTTTTGT[G/T]TTTTTTTTTTGTCAT	88455
rs569223355	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998954	AGTAGAAATATCCCC[C/T]TTTATGCAAATACTG	88455
rs569337164	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997303	AGAATCGCTTGAGCC[C/T]GGGAGGTGGACGTTG	88455
rs569373387	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038666	CAATCTTTTTATTAT[C/T]TGTAAAAGATATAAA	88455
rs569415403	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110030963	AGCCGGGTGTGGTGG[C/T]GCATGCCTGTAATCC	88455
rs569462036	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110023496	GTGACTCAGCTATTT[G/T]GCAGACCTAATGGCA	88455
rs569569886	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021526	CGCCTACCGGGTTCA[A/G]GCAATTCTCCCACTT	88455
rs569627464	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110012808	CTGCCTGCCAGGTCT[A/G]CATATAACCACAGTT	88455
rs569677371	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028928	TTTTTAGTAGAGATA[A/G]GGTTTCACCATATTG	88455
rs569727560	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005415	AGATTACAGGTGTTA[G/T]CCACTGCACCCACCC	88455
rs569747923	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110024534	GCACAGCCCATTTGC[A/C]TGACATCAGTGCATT	88455
rs569828151	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017381	TATTTCTCTAAAGTA[C/T]TACGTAGGCAGTTGA	88455
rs569927137	snp	C/G/T	0.00239393	0.0345281	intron-variant	ANKRD13A	GRCh38.p7	12:110011274	TGCAGGTGCCAAAAG[C/G/T]GGGGCGAGAGTGGCA	88455
rs569950465	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004406	GGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAA	88455
rs569991507	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003248	AGAGCCAGGCTCCCT[A/G]TTTAGGAAGCCAGCA	88455
rs570006157	in-del	-/A	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110036585	AACCCTGTCTCTCCT[-/A]AAAAAAAATACAAAA	88455
rs570234015	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036706	AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG	88455
rs570414825	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030127	GAACCCTGGCTTGAT[C/T]ACTTACTCACTGTGA	88455
rs570509441	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110011969	TATTTTAATGTAATA[C/T]ATCCAATTATGTAAA	88455
rs570539608	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032704	ACGACCCAAATGTCC[C/T]GAGATGGTAGAATGC	88455
rs570604415	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025270	CTGAGGCACGAGAAT[C/T]GCTTGAACCCAGGAG	88455
rs570659051	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998244	CCCACGCATTCCATG[A/G]TTAGAGTCTCCGGGT	88455
rs570731819	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019608	ATGTGCCCTTTCTAG[C/T]GGATTTTACTTGAAT	88455
rs570838914	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004171	TCAAAAAAAAAATAA[A/T]TTTTTTTTAAGGCTT	88455
rs570861565	in-del	-/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110023566	CCTGCTCTTTTGTAA[-/G]GAGCAGGATGGTCTG	88455
rs570894514	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035641	TTTTAGTAGAGACGG[C/G]GTTTTACCATGTTGT	88455
rs570932200	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003404	TGAAGAGCCTAGAGC[C/T]TGCTCTCCTCATGTG	88455
rs570997739	in-del	-/G	0.00970784	0.0689904	intron-variant	ANKRD13A	GRCh38.p7	12:110023958	TCACTAACTTAAGCT[-/G]GGGGGGAAAAAAACT	88455
rs571024020	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028997	CGCCTGGGCCTCCCA[A/G]ACTGCTGGGATTACA	88455
rs571197795	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037818	TCCATTAGCTGTATT[A/G]GCTTGCAGGTCACAT	88455
rs571221681	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035988	TGCTTTTCGTTGTGT[A/G]TATCTTCCACGTGGG	88455
rs571244481	in-del	-/C	0.00279162	0.0372561	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997713	CCTGCTGGATAGTAA[-/C]CCCCTCAGTAAATAG	88455
rs571268798	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110003379	TGAGCCATGGGCTAG[A/G]CATCCAAGATGAAGA	88455
rs571289641	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035104	GACCCCAAAGCAAGC[A/G]TGTTCCCTTTGGGAG	88455
rs571298281	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016643	TCTTCCCCGCCATGC[A/G]TAGGACTTTTCCTCC	88455
rs571451413	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110020022	TGGAGACCACTGATC[C/T]GAGGGAGTCCTAAGA	88455
rs571474576	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028063	GATTCAGGACTTTAT[A/C]TTGCAACAGAGCACC	88455
rs571478504	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110027263	TTCCTTAGAGTTATT[A/G]AGAGGATTAGATGAG	88455
rs571512738	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110011314	CGAAGAGGTAAGAGC[C/T]AGGTGTGCATGTCTA	88455
rs571560261	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017656	TGGCATACTTAGGCC[A/G]GATGCGGTGGCTCAT	88455
rs571589074	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018729	TGTCTGCTTCACTTT[A/C]CTGAGCCTTTGAGCA	88455
rs571792078	snp	A/G	0.0111196	0.0737302	intron-variant	ANKRD13A	GRCh38.p7	12:110011144	ACTTTCCAAAAGTCC[A/G]TGGCAGTTTGTTGTA	88455
rs571842684	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027293	GTTACGACGTGGAAG[C/G]CTTTAGAATGGCGCC	88455
rs571929832	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028050	GGAACTTAAAAAGGA[C/T]TCAGGACTTTATATT	88455
rs571942531	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018844	ATTTCTGTGAATTCT[A/G]TAATAATATATTTTA	88455
rs572003058	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110022059	CATCTTCGGATGCTT[C/T]TGCATGCAAAGTTAC	88455
rs572095897	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000800	TTCGCTCTTGTTGCC[C/T]GGGCTGGAGTGCAAT	88455
rs572125153	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110025065	TAGTATTACAAGACT[A/G]CCAGCGGAGGCTGGG	88455
rs572232492	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:109999868	TGAGCCCATTTCCAG[A/C]CCTCTGTCCCCGGGA	88455
rs572310741	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035203	AGCTTAGCTCCCCCC[A/G]CCAGCTCCCAAGTAG	88455
rs572426721	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014546	TAAATGACCTGCGTA[C/T]TTAGTGGCTCCAGAA	88455
rs572934381	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003940	AAGGCAGGTGGATCA[C/T]GAGGTCAGGAGTTCA	88455
rs572955917	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039535	AGAATGCCTCACTTC[A/G]CTCAGTTCATCACTG	88455
rs572993224	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110015967	TCTTTTTTTTTTTTT[C/T]TCCATACAGTATCTC	88455
rs573054909	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032851	AATTTGAAGAATAAA[C/T]TCCGCATGATTCCAT	88455
rs573089954	snp	A/C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015162	AAATAATCCTAAACA[A/C/G]GGCTGCTGTGGTAGT	88455
rs573125564	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025072	ACAAGACTACCAGCG[A/G]AGGCTGGGTGCAGTG	88455
rs573184967	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022575	CGCCGTCTTCCCAGC[A/G]TGCATGAAGGGTGAG	88455
rs573273487	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013177	GGTGTACACAGTTCT[C/T]CAACATCGAGACTAC	88455
rs573288377	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022210	ATTCCAGCACTTTGG[G/T]AGGCTGAGGCGGGTG	88455
rs573354434	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110001249	TGGCTCAAAATTGGT[-/G]CTATAATTGTCAAGA	88455
rs573492258	snp	G/T			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997416	AAAAATAACAAAAAA[G/T]AATATATTAGATGAT	88455
rs573523664	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998675	AGCTTAAAAATGACA[C/T]TCATACATGGACTAA	88455
rs573540066	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110013899	TGTTTTCTTGAAAGT[A/G]GCCTCCTGAGCATCT	88455
rs573540248	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110005882	AGTGCAGTGGCATGA[A/T]CTCAGCTCTCTGCAA	88455
rs573558185	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034036	GTGTTTGGCTAATCT[G/T]AAAGATTTATTCTAA	88455
rs573626214	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028978	CCTGACCTTGTGATC[C/T]GCCCGCCTGGGCCTC	88455
rs573680787	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110025184	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	88455
rs573772351	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110009103	TTTTATTTTTTGAGA[C/T]GAAGTTTTACTCTTG	88455
rs573826456	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110023940	ATGATTTCCAAGTGT[C/T]CTTCACTAACTTAAG	88455
rs573940329	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006743	CTGGGATTACAGGCA[C/T]GCGCCACCATGCCTG	88455
rs574008482	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016875	TCTCCCAGATTCAAG[A/C]GATTCTCATGCCTCA	88455
rs574076206	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110014215	CAGGAGACCGAGACC[A/G]TCCTGACTAACACGG	88455
rs574147727	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004686	TGTTCTCTGAACTCA[C/T]ATTATTAGTTGAAGA	88455
rs574190431	in-del	-/T	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110030239	TGGCATGATCTTGGC[-/T]CACTGCAACCTCTGC	88455
rs574225078	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110007306	TGTCATTTTAACAAT[A/G]TTGTCTTTTAAACCA	88455
rs574260781	snp	A/G	0.00606163	0.0547181	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999657	CCGAGACTTGGGGCG[A/G]GCGACGAGGACCAGG	88455
rs574297556	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110031455	CTCCCAGGCTCAAGC[A/G]ATTTTCTTGCCTAGT	88455
rs574401734	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998889	AGGACCGGACAACCC[C/T]CACACAAAAACTGCC	88455
rs574425988	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012962	CTATGTTTTTTACTC[A/G]GTGAAGAGCTAGCAA	88455
rs574430827	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030498	CAATCTCAGTTTTCC[C/T]GTCTGTGTATTGGGA	88455
rs574622807	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038771	AGTAGTTAACTCTCT[C/T]TTGTCAAACCCTCTT	88455
rs574718949	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039226	TGGCTGCAGTGAGGC[C/T]GTGTCATTGGCTCAC	88455
rs574869337	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007538	GACATGTGCCACCAC[A/G]CCCGGCTAATTTTGT	88455
rs574891790	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037980	TAAAGTGTGATCTAT[A/G]AGAATTGGAGACACT	88455
rs574924916	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012436	ATACTTTTCCTTGGA[A/G]TCATCTTTATCTTAA	88455
rs575045389	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020248	AGCTCTCTGCAAGCC[A/T]AAGTAGCTTACCCTG	88455
rs575059632	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021032	GGCTGTTACCCCACT[A/G]AGTATAAATGGGAAA	88455
rs575144040	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039430	GAGGGTGCTCATACA[A/G]AATTCCAGTCTTTGA	88455
rs575189822	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023025	GAAGAAAAGCAAACT[A/G]TTTGGAAACAAAATG	88455
rs575253185	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110006346	TTTTGTTTGTACGCA[C/T]CCTAGTGGGTGTGAA	88455
rs575316855	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997756	TTATGGATATTGCTA[G/T]TATTTTCTAATTACT	88455
rs575393512	snp	A/G/T	0.00010301	0.00717605	intron-variant	ANKRD13A	GRCh38.p7	12:110023967	TAAGCTGGGGGGGAA[A/G/T]AAAACTATAAAGGCT	88455
rs575446510	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004214	AGTGGATGAGCTGAA[A/G]TGAGCAAATAGGAAG	88455
rs575597345	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030406	TCCTGACCTCAGGTG[A/G]TCAGCTCGCCTTGGC	88455
rs575695821	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110019073	ATACATTTTAACATA[C/T]GAAGCTTCCTTGTTT	88455
rs575739739	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005809	CTGTGTGTATTTGTG[C/T]ATATGTTTTTGTGGG	88455
rs575757595	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020113	CCTGAGAAAATGGAC[A/G]CTATCATCCTGATAG	88455
rs575940058	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110011419	TCCGCATACGTGCCC[A/G]GCAGATCATGCTTGC	88455
rs576101215	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110021234	TTGTCGTGCATTGAG[C/G]AAGAATTGAGCCACT	88455
rs576117266	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010941	AGATGTATTATGGCA[G/T]TTAAAAAGTTTTTAC	88455
rs576149151	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110021001	TGCGATTTGTGAAGA[C/G]AGGGTGACAATTCCT	88455
rs576231724	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027596	TCAGCCAGTCTGTAA[C/T]TGCATTTCCTAATGA	88455
rs576369895	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026743	AAAAATTAACCAGGC[A/G]TGGTGGCGCACTCCT	88455
rs576412434	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004445	ACACAGAGAAACCCC[A/G]TCTCTACTAAAAATA	88455
rs576437895	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110001097	CAACAATTCTGGGAG[A/G]TATTGGTGCCCTCAA	88455
rs576474204	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110001659	CCCTGGCCTCAAGCA[A/G]TCCGCCCACCTCTAC	88455
rs576550824	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012256	TGTAGTACCAGCTAC[C/T]CAGGAGGCTGAGGGG	88455
rs576636362	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038699	CAACTCCCATCAGTA[A/G]CAATACAAGGTTATA	88455
rs576650321	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035363	TAATCCCAGCACTTT[G/T]GGAAGCCAAGATGGG	88455
rs576771584	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038134	CCAGCTAAAGTTAGA[A/G]GAGATACATATAGAA	88455
rs576977206	snp	C/T	1.64863e-05	0.00287104	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029625	CCCACCTGGATTTCC[C/T]GTCAAAATAGGTACT	88455
rs577053359	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019621	AGTGGATTTTACTTG[A/T]ATCCTATTTTTGTCT	88455
rs577156529	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110013422	TTGTGGAAATGTGAG[C/T]TCTTTTACAAATTAC	88455
rs577498777	snp	C/T	6.59217e-05	0.00574078	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019200	CACCACCGAACGCTT[C/T]GACCTTTCCCAAGAA	88455
rs577552071	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000932	CCGGCTAATTTTGTA[G/T]TTTTAGTAGAGATGG	88455
rs577566144	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110026510	TGAACCTGGCAGGCG[A/G]AGGTTTTGGTGAGCT	88455
rs577605920	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008106	ATCCAGTCTTTCACC[A/G]TTAACTATGATGTTA	88455
rs577665267	snp	A/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110031119	CTCAAAAAAAAAAAA[A/T]TATAATTCAGTCATC	88455
rs577673838	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015112	AACTTTTAGATTTCT[A/G]AATCTTTAGGAACTT	88455
rs577704526	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026097	CTCCTGAGTAGCTGG[A/G]ATTACAAGCACCCAC	88455
rs577736950	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015808	CGCCTCGGCCTCCCA[A/G]AATGCTGGGATTACA	88455
rs577752453	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110025929	ATGTGATTGGGTTGT[A/G]TTAAGCCTAACCCTA	88455
rs577806972	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002463	CTCTACTAAAAATAC[A/G]AAAATAGCTGGATGT	88455
rs577969804	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110017926	GACAGGGTGAGACTC[C/T]GTCTCAAAAAAAAAA	88455
rs578048706	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007430	TTGTTGCCCAGGCTG[A/G]AGTTCAATGGCACAA	88455
rs578068162	in-del	-/TG	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110033582	GTATTTTTTTATGAC[-/TG]TGTTCGTTGTTTCCA	88455
rs578078424	in-del	-/TT	0.0168382	0.0901973	intron-variant	ANKRD13A	GRCh38.p7	12:110016281	TCTTCTTATTTTCTC[-/TT]TTTTTTTTTTTTAAC	88455
rs578162949	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:109999792	AGGGCCAGGTGAGGG[A/G]CGGGGCGGGGGTCCG	88455
rs578213459	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110020964	TCAACAGTAGAGTTG[A/C]CAGAGTCATTGTTTG	88455
rs745327920	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010241	GTAAGTAGTTTCCCC[C/T]TTCCCATGATAAACA	88455
rs745337377	snp	A/G	4.94841e-05	0.00497389	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019268	GCAGGGAAGTTGAGC[A/G]GCGGCTCACAAGCCC	88455
rs745385591	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009279	AGAGACGGGGTTTCT[C/T]CATGTTGGTCAGGCT	88455
rs745388390	in-del	-/TGTGGGTGGCAGCA	3.32621e-05	0.00407798	intron-variant	ANKRD13A	GRCh38.p7	12:110029683	GGTTCTGCCCATGTT[-/TGTGGGTGGCAGCA]TGTGGGTGGCAGGAT	88455
rs745482035	snp	C/T	1.82583e-05	0.0030214	intron-variant	ANKRD13A	GRCh38.p7	12:110019357	CTCTAAATTTTAATG[C/T]CTAATCCCCATGCTG	88455
rs745485664	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029828	TGGTTCATTTTGTGT[A/G]TCAAAGTCAAGAGAT	88455
rs745518438	snp	C/G/T	4.95465e-05	0.00497707	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037412	TGTGCCCCAGCGCCC[C/G/T]GAGCGAGACAAGCCG	88455
rs745593819	snp	C/T	1.64768e-05	0.00287021	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013181	TACACAGTTCTCCAA[C/T]ATCGAGACTACCACA	88455
rs745611149	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014397	AGCCTGGGTGACAGA[G/T]CGAGACTCCATCTCA	88455
rs745782030	snp	A/G	1.64757e-05	0.00287012	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029599	CTGAGAGATTTCATC[A/G]AATTGGAATTCCCAC	88455
rs745806879	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002905	CTGTCTCACTAATAG[C/T]AGGCAGTTGTGTAAC	88455
rs745825593	snp	A/C	1.64874e-05	0.00287113	intron-variant	ANKRD13A	GRCh38.p7	12:110030622	TAAAGTTTACTTATA[A/C]AAGTTTTTATTTTGT	88455
rs745887423	snp	C/G	1.65051e-05	0.00287267	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018485	TTTATATTTAAGGGA[C/G]AAGGTGAGTGACTTC	88455
rs745908378	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039263	GACTCATAGGTAATT[C/T]CTGTGTTTGCATTCC	88455
rs746017735	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110006447	TTATTGGCAATTTGT[G/T]TATCTTCCTTGGAGA	88455
rs746075981	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010638	AAGGTATTTTAGCAC[C/T]GGGGGAACACTGAGG	88455
rs746086710	snp	C/G/T	3.29686e-05	0.00405998	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033846	TGTGTTTGAAATTCC[C/G/T]GAATCTTACTATGTT	88455
rs746097284	snp	C/G	1.82587e-05	0.00302142	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033996	TGGCAGGGCGTGGGA[C/G]GTCTTACCCTCTGGG	88455
rs746152474	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110011643	ATGTGCTTGAGAAAT[A/C]CCCCATGTTCAGTGT	88455
rs746171689	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038804	ATATAACCATCGCAC[A/G]ACATACAGAACCCTG	88455
rs746190703	in-del	-/CAGT			intron-variant	ANKRD13A	GRCh38.p7	12:110014126	TTATTATAAATAAGA[-/CAGT]CAGCTGGGTGTGGTG	88455
rs746192784	snp	C/T	6.61616e-05	0.00575121	intron-variant	ANKRD13A	GRCh38.p7	12:110027791	AGCAATGAGCTTTCA[C/T]TGCAGTTAGATGAAA	88455
rs746205538	snp	C/G	1.65438e-05	0.00287605	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037497	ATGGGAGCTCCGGCT[C/G]CAGGAGGAAGAGGCT	88455
rs746331456	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035295	AGTATTGAATTGTGT[C/T]TTCTAATCTTGCCCT	88455
rs746346994	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018245	GATGGTCACCATCTT[G/T]CCACTCCCCTCCTTT	88455
rs746358295	snp	C/T	3.29489e-05	0.00405874	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028549	CTGCAAACAACCCCA[C/T]AGCCATCACGCCTGA	88455
rs746448236	snp	C/T	3.29489e-05	0.00405874	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018410	AGTGGTGCCAAACTG[C/T]GCGTCGATATCACAT	88455
rs746469389	snp	G/T	1.65603e-05	0.00287747	intron-variant	ANKRD13A	GRCh38.p7	12:110011971	TTTTAATGTAATACA[G/T]CCAATTATGTAAATG	88455
rs746476099	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019468	TGGGTTTTAAGATTG[A/T]TCTCTAACCAGTAGA	88455
rs746479037	snp	A/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038994	TAACGTCTGTATCAT[A/T]CAGTTAGTGTTGCCA	88455
rs746536646	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110006861	TTGGCCTCCCAAAGT[G/T]CTGGGATTATAGGGA	88455
rs746611484	snp	C/G	3.33572e-05	0.00408381	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012101	TTACTCCGACATAAA[C/G]CAGATGTGACAAAAG	88455
rs746632017	snp	A/G	1.65523e-05	0.00287678	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037501	GAGCTCCGGCTCCAG[A/G]AGGAAGAGGCTGAGC	88455
rs746646331	snp	C/T	3.29478e-05	0.00405867	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028558	ACCCCACAGCCATCA[C/T]GCCTGATGAGTACTT	88455
rs746653894	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007666	ATTACAGGTGTGAGC[C/T]ACCACACCAGGCCAG	88455
rs746740001	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028776	GGAGTCTCGCTCTGT[C/T]GCCTAGGCTGGAGTG	88455
rs746761196	snp	A/T	8.99139e-05	0.00670439	splice-acceptor-variant, intron-variant	ANKRD13A	GRCh38.p7	12:110030643	TTTATTTTGTTTGTT[A/T]GAAATTCCCTTGTTT	88455
rs746783240	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009724	TTATCCAAGAAATGT[A/G]TGCTGCTCTGTGGCT	88455
rs746791158	snp	A/G	1.67621e-05	0.00289495	intron-variant	ANKRD13A	GRCh38.p7	12:110013085	GTTTTGGAATTTGTC[A/G]GAAAGTATGAGAATT	88455
rs746901473	snp	A/G	0.000132046	0.00812438	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019280	AGCGGCGGCTCACAA[A/G]CCCTGTCATTAACAC	88455
rs746922617	snp	A/G	2.1918e-05	0.00331037	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030758	ACCCAGGCTGATTCA[A/G]GTAAAAAAATAAATA	88455
rs746978240	in-del	-/AT			intron-variant	ANKRD13A	GRCh38.p7	12:110012776	GTTGACTGAGCAGGG[-/AT]ACTGTAGGCCAAGCC	88455
rs747035934	snp	A/G	0.000141054	0.00839684	intron-variant	ANKRD13A	GRCh38.p7	12:110021074	TCCATTTGTACCGAG[A/G]ACTAAGGCACATTTT	88455
rs747051941	snp	C/G	0.000131684	0.00811324	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034005	GTGGGAGGTCTTACC[C/G]TCTGGGTTAGCCTCA	88455
rs747114251	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037858	CAGCTTTAGACAAAA[C/T]CCCAATCCCCGCAGG	88455
rs747118055	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000294	CTGGCCGACGTTAAC[G/T]TAGCTGTAGAATGAG	88455
rs747125668	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002706	TGGTGAGTTTCTGCT[A/G]TCAGTTTCCTCATTC	88455
rs747213513	snp	A/C/G	3.31698e-05	0.00407235	intron-variant	ANKRD13A	GRCh38.p7	12:110025711	GTTTTGATTCCCTGT[A/C/G]TCACTGTTTTCTTTC	88455
rs747299244	snp	A/G	3.29794e-05	0.00406061	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025813	CGAGGAGGAAAAAAA[A/G]AGATATAAAGGTAAT	88455
rs747326053	snp	C/T	1.67321e-05	0.00289236	intron-variant	ANKRD13A	GRCh38.p7	12:110013093	ATTTGTCAGAAAGTA[C/T]GAGAATTAAATTTCA	88455
rs747331296	snp	C/T	1.64743e-05	0.00287	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018415	TGCCAAACTGCGCGT[C/T]GATATCACATTGCTG	88455
rs747350769	snp	A/G	1.64961e-05	0.00287189	intron-variant	ANKRD13A	GRCh38.p7	12:110028663	AGAGGTTCAGCTGCC[A/G]TTTTCAACCTATGTA	88455
rs747357087	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021610	TTTGTATTTTTGTAG[A/T]GGCGGGGTTTCACCA	88455
rs747378598	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010539	TTTGGAATTCTCCAT[C/T]TCTTTGGTGCGATGG	88455
rs747386978	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018072	CTTATATAGTGGGGA[C/T]AGACCCCACTATAAA	88455
rs747487940	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032342	CTCCCCTGTAGTCTA[C/T]CAGTAGGAGGAATTA	88455
rs747557809	in-del	-/TTGT			intron-variant	ANKRD13A	GRCh38.p7	12:110020973	GAGTTGCCAGAGTCA[-/TTGT]TTGTTGAAGTGCGAT	88455
rs747601121	snp	C/T	2.64834e-05	0.00363882	intron-variant	ANKRD13A	GRCh38.p7	12:110012181	TCCGTCTGAGCACCA[C/T]GGTGAAACCCTGTCT	88455
rs747622655	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034570	GCCTCCCAAGTAGCT[-/G]GGACTAAAGTCATGC	88455
rs747748362	in-del	-/CT			intron-variant	ANKRD13A	GRCh38.p7	12:110013603	ACAAACAAAGCAAGA[-/CT]CTGTCTCTAAAAAAA	88455
rs747749163	snp	A/G/T	8.65994e-05	0.00657975	intron-variant	ANKRD13A	GRCh38.p7	12:110019117	ACTTTGCACTTAGTT[A/G/T]TGCCTTTGTTTCCAT	88455
rs747779310	in-del	-/TG			intron-variant	ANKRD13A	GRCh38.p7	12:110017807	ATGATGGTGGGTGCC[-/TG]TGTAATCCCAGCTAC	88455
rs747783874	snp	A/G	1.65198e-05	0.00287395	intron-variant	ANKRD13A	GRCh38.p7	12:110028678	ATTTTCAACCTATGT[A/G]TGTTTCAGAAATTGT	88455
rs747800671	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006242	TGCCAGCAATTTTTC[A/G]AAGTGGCTGCACTAT	88455
rs747802155	snp	A/C	4.94246e-05	0.0049709	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029562	TGACCTAATGGCTCG[A/C]ACGAGTGCTCATTTT	88455
rs747900770	snp	A/C			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038695	AAAACAACTCCCATC[A/C]GTAGCAATACAAGGT	88455
rs747948040	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027097	CTATTGTGATGAAAG[A/G]TTTAGACAGAACTTG	88455
rs748093013	snp	A/G	1.66344e-05	0.0028839	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037533	CCAGCAAGTCTTACA[A/G]CTGTCACTCACTGAC	88455
rs748172741	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012906	GTAAGAATAGGGGTC[A/G]GGAGAGGTGGACGGG	88455
rs748184822	snp	C/G	3.30978e-05	0.0040679	intron-variant	ANKRD13A	GRCh38.p7	12:110025835	AAAGGTAATCACCAC[C/G]ACCCTCCCACCTCCT	88455
rs748227905	snp	A/G			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109999117	AGCTGGAATGGTTTG[A/G]TCCGGGGCTCAGTTG	88455
rs748271339	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025964	TTCTCTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT	88455
rs748348102	snp	A/G	4.94271e-05	0.00497102	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013199	CGAGACTACCACAAC[A/G]CATCCATGGCCCTTG	88455
rs748355677	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036606	AAATACAAAAAATTA[G/T]CCGGGCATGGTGCCA	88455
rs748378392	snp	C/G	1.65236e-05	0.00287429	intron-variant	ANKRD13A	GRCh38.p7	12:110027771	GTGCACAAGGGGTAA[C/G]TTGAAGCAATGAGCT	88455
rs748435968	snp	C/T	1.648e-05	0.0028705	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016392	CTGCCCTTCAGGCTC[C/T]GGATTTCTATGTGCA	88455
rs748473229	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110014725	TTCTTTGGTAAAAAT[C/G]ATGGCAAAGCCTTGC	88455
rs748494840	snp	A/G	1.65636e-05	0.00287776	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019166	AGTTAATGGAAGTCA[A/G]CCATGATGACAAAGT	88455
rs748558495	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008444	ATATCATAAGAGATA[C/T]TAGTGTGTGGTTTTC	88455
rs748596382	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009361	GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCC	88455
rs748643633	in-del	-/AACCA			upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999180	CCCAGTTGTGGACCG[-/AACCA]CATGGGGCTACTGGA	88455
rs748678829	snp	C/T	3.29473e-05	0.00405864	intron-variant	ANKRD13A	GRCh38.p7	12:110036228	CAATTTCTCCTAAGA[C/T]GTATTCATGTCTATC	88455
rs748752939	snp	G/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029571	GGCTCGAACGAGTGC[G/T]CATTTTGCAAGACTG	88455
rs748885125	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110032275	TTACCATTTTTAAGT[A/G]TTGATTTTTGTGAGA	88455
rs748914527	snp	A/C/T	3.29768e-05	0.00406048	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019190	ACAAAGTGGTCACCA[A/C/T]CGAACGCTTCGACCT	88455
rs748914557	snp	A/G	0.000118687	0.00770257	intron-variant	ANKRD13A	GRCh38.p7	12:110030610	TGTTATTCTCAGTAA[A/G]GTTTACTTATAAAAG	88455
rs748914586	in-del	-/A	6.68472e-05	0.00578093	intron-variant	ANKRD13A	GRCh38.p7	12:110012161	CTTTTACAATAATTT[-/A]AAAGTCCGTCTGAGC	88455
rs749004301	snp	A/G	1.64876e-05	0.00287116	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019258	AAGCCAAAAAGCAGG[A/G]AAGTTGAGCGGCGGC	88455
rs749004666	in-del	-/C	3.30622e-05	0.00406571	intron-variant	ANKRD13A	GRCh38.p7	12:110029430	CAATAATCTCCTTTT[-/C]CCATCTGGTGGAGAT	88455
rs749042244	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017663	CTTAGGCCGGATGCG[G/T]TGGCTCATGCCTGTA	88455
rs749042310	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003127	TTACTGATGGTGAGA[C/T]ATGAACACTTAAGGG	88455
rs749046410	snp	A/G	5.24242e-05	0.00511951	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012123	TGACAAAAGAAAATC[A/G]CCAGGGATGGACAGG	88455
rs749193512	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024444	GGAAGGATTAGACTT[C/T]ACATGTGTTCAAATG	88455
rs749276610	snp	A/T	1.64787e-05	0.00287038	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016421	CAGATGAAATGGGAA[A/T]TCACCAGCTGGGGTG	88455
rs749320147	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026901	AAAAGAAAAAGGAAA[A/G]AAAATTTCCTTAGTC	88455
rs749343626	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110024332	AGCTATGCTAAAGAG[-/A]AACAATATGGTAGAG	88455
rs749491845	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018386	AATGATGTCTGTCGC[A/G]TCTGGAAAAGTGGTG	88455
rs749627556	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035509	GGCTGCAGTGCAGGG[A/G]CACAATATTGGCTCA	88455
rs749630116	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036507	ATAATCCCAGCATTT[C/T]GGGAGGCCGAGGCAG	88455
rs749677135	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019973	GGGGGGCCTTTGAGT[A/G]GAGGCTGTCAAAGCT	88455
rs749760165	snp	A/C/T	4.96063e-05	0.00498007	intron-variant	ANKRD13A	GRCh38.p7	12:110027785	AGTTGAAGCAATGAG[A/C/T]TTTCATTGCAGTTAG	88455
rs749787531	snp	C/T	1.65762e-05	0.00287886	intron-variant	ANKRD13A	GRCh38.p7	12:110025842	ATCACCACCACCCTC[C/T]CACCTCCTGTTTTGT	88455
rs749843836	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008096	GAGGGGAAACATCCA[A/G]TCTTTCACCATTAAC	88455
rs749855973	snp	C/G	0.000186525	0.00965546	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030745	AAATGTGGAAGGGAC[C/G]CAGGCTGATTCAGGT	88455
rs749897281	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022120	ATTTAAAACAGGGTA[G/T]GAACATTGGGTTGAA	88455
rs749904455	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023634	GCTACTTGTGGAGAT[C/G]CCACCATTGACATGC	88455
rs750060989	snp	C/G	1.67052e-05	0.00289004	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033801	TTTTGTTTCAGCTTC[C/G]CACATCACAAACTTT	88455
rs750114809	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110011311	GAACGAAGAGGTAAG[A/C]GCCAGGTGTGCATGT	88455
rs750151595	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011923	TGTTTTCTATTTTTT[-/G]TACTTGAAATATCTG	88455
rs750162015	snp	C/T	3.30196e-05	0.00406309	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027748	GGGAACTGTGGAACA[C/T]CAATTTGGTGCACAA	88455
rs750163831	snp	A/G/T	0.000115663	0.00760395	synonymous-codon, missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037419	CAGCGCCCTGAGCGA[A/G/T]ACAAGCCGTTTTGAT	88455
rs750188868	in-del	-/TTTTAAGAT			intron-variant	ANKRD13A	GRCh38.p7	12:110019456	ATAAACACTAGTGGG[-/TTTTAAGAT]TTTTAAGATTGATCT	88455
rs750252041	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032960	AGTGTAAACAACTAT[C/T]CTGAATTATGTATTT	88455
rs750264980	snp	G/T	1.64866e-05	0.00287106	intron-variant	ANKRD13A	GRCh38.p7	12:110016375	CTGTTTTAAACCTTT[G/T]TCTGCCCTTCAGGCT	88455
rs750268687	in-del	-/TG			intron-variant	ANKRD13A	GRCh38.p7	12:110034445	AAGCAGTAGGCTTTG[-/TG]TGTGTGTGTGTGTGA	88455
rs750307343	snp	A/G	3.29755e-05	0.00406038	intron-variant	ANKRD13A	GRCh38.p7	12:110016452	AGTGGCTGTGGGCTC[A/G]TTATTTATTTCTCTT	88455
rs750374721	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017608	TTTTTTCTAATGCAC[A/G]TAGTCACTCTTATTT	88455
rs750378957	snp	A/G			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034333	TGAAGGTAGTGAAGT[A/G]GATTTGAATCCCACT	88455
rs750385959	snp	C/T	1.6489e-05	0.00287128	intron-variant	ANKRD13A	GRCh38.p7	12:110018339	TAGTACACTTCTCTC[C/T]TCCAGTGCCCTTGGT	88455
rs750398094	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018481	TAGTTTTATATTTAA[A/G]GGAGAAGGTGAGTGA	88455
rs750432364	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018714	GTTACCCTTGTGATG[A/T]GTCTGCTTCACTTTC	88455
rs750473015	snp	C/T	8.23635e-05	0.00641677	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029520	AGAGTTTCCCCTCTC[C/T]CTGGTGGAGCAGGTC	88455
rs750533830	in-del	-/TAAAA	3.37898e-05	0.0041102	intron-variant	ANKRD13A	GRCh38.p7	12:110024128	GTAAAAGGAAACTCT[-/TAAAA]TAAGATTTAATATAG	88455
rs750551347	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007115	AGCTTTGTGTAGTAC[A/G]TTTTAAAATTGGCAA	88455
rs750575602	in-del	-/TT	1.6473e-05	0.00286988	intron-variant	ANKRD13A	GRCh38.p7	12:110036247	TTCATGTCTATCACA[-/TT]TGTCTTTGCCAGGAA	88455
rs750689035	snp	C/T	3.37479e-05	0.00410765	intron-variant	ANKRD13A	GRCh38.p7	12:110024125	AAGGTAAAAGGAAAC[C/T]CTTAAAATAAGATTT	88455
rs750707743	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026974	GTAATTAAAGCTATT[C/T]GTGAGGGCTTGTTTA	88455
rs750885131	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013363	TTCTGATTCGTGAAT[A/G]TGAAATACTCAATAC	88455
rs750902538	snp	A/G			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998821	CATGTTTTGGGGAGT[A/G]CTACTGGCATTGAGT	88455
rs750983664	snp	A/G	1.67374e-05	0.00289282	intron-variant	ANKRD13A	GRCh38.p7	12:110023999	CAGATATAAATCTGA[A/G]TGGCATATTGTACAT	88455
rs751039345	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037203	TCTCACCCGTATACA[A/G]CACCTACACCGCCAG	88455
rs751147796	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023606	GTTCTAAGAATTCCT[C/T]GAGTGAGATGTGGCT	88455
rs751199829	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022070	GCTTTTGCATGCAAA[C/G]TTACCAAGGGCCACA	88455
rs751225788	snp	A/C	1.70499e-05	0.0029197	intron-variant	ANKRD13A	GRCh38.p7	12:110024141	CTTAAAATAAGATTT[A/C]ATATAGCTATTTAGC	88455
rs751254825	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023299	TGGTTCCTAAATACA[A/T]TTTTTTTCAGGAGTA	88455
rs751254939	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009238	AGGCATGTGCCACCA[C/T]GCGCGGCTAATTTTG	88455
rs751282029	snp	A/G	2.55073e-05	0.00357113	intron-variant	ANKRD13A	GRCh38.p7	12:110012175	TTAAAGTCCGTCTGA[A/G]CACCATGGTGAAACC	88455
rs751295658	snp	A/G	1.64773e-05	0.00287026	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018359	GTGCCCTTGGTTTCT[A/G]GAATATGCCCAAATG	88455
rs751306654	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028606	TGAAAGACAGGGACA[C/T]TGGAAGGCCGAAAGA	88455
rs751308864	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110025195	ACCCCGTCTCTACTA[A/C]AAATACGAAAATTAA	88455
rs751313743	snp	C/T	1.65192e-05	0.00287391	intron-variant	ANKRD13A	GRCh38.p7	12:110025734	TTTCTTTCGCATACA[C/T]CTCTCAGGTTTACAC	88455
rs751350192	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012835	AGTTACATGTTGTGT[A/G]ATCGTATAGTTAAAG	88455
rs751385441	snp	C/T	1.64849e-05	0.00287092	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018466	GATAAGAGGGAGGCG[C/T]AGTTTTATATTTAAG	88455
rs751401942	in-del	-/GAGTA			intron-variant	ANKRD13A	GRCh38.p7	12:110019969	CATGGGGGGGCCTTT[-/GAGTA]GAGGCTGTCAAAGCT	88455
rs751505145	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015766	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTA	88455
rs751544802	snp	C/G	1.65187e-05	0.00287386	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033826	AACTTTGAGGTTGAT[C/G]AATCTGTGTTTGAAA	88455
rs751631195	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019231	ATGGAGCGCCTCACT[C/T]TGGACTTGATGAAGC	88455
rs751762400	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110036314	GACAAACACCTATGA[C/T]GCCCAGTATGAGAGG	88455
rs751802235	snp	C/G	1.64814e-05	0.00287061	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013157	AGCACTGGCGATCCT[C/G]AGATGGTGTACACAG	88455
rs751848363	snp	G/T	3.31252e-05	0.00406958	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037360	GTTTTCCAACCCAGG[G/T]CCATCCAGGAGAGCC	88455
rs751880062	snp	A/G	0.000178492	0.00944532	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999658	CGAGACTTGGGGCGG[A/G]CGACGAGGACCAGGT	88455
rs752009775	in-del	-/C	0.000132028	0.00812384	intron-variant	ANKRD13A	GRCh38.p7	12:110027689	ATTAGACTTTAAACT[-/C]CCTACCCCTCTGTAG	88455
rs752097973	in-del	-/GC	1.6513e-05	0.00287336	frameshift-variant, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037450	AATGACTTGCAGCTA[-/GC]CATGGAGCTCTCTGC	88455
rs752102841	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011540	TGGGAATCCAGCTAG[A/G]GAATGTAATTTTATT	88455
rs752153154	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023117	CATGACATCCCAACC[A/G]CTCAGTGGTCAGAGC	88455
rs752155809	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012592	ACTTCTTCCACCATA[C/T]ACGAATGTGGAGGCC	88455
rs752174444	snp	A/C			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998485	CAGCTGAGCTGAAGC[A/C]GCAGCAGAAAGTTCA	88455
rs752194559	snp	C/T	1.64874e-05	0.00287113	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025756	GGTTTACACAGTAAA[C/T]AATGTGAATGTGATC	88455
rs752451904	snp	C/T	1.65154e-05	0.00287358	intron-variant	ANKRD13A	GRCh38.p7	12:110013296	TGAGCTAAATGCTGA[C/T]ACAATTACTGGAGAC	88455
rs752473801	snp	C/T	1.74221e-05	0.00295139	intron-variant	ANKRD13A	GRCh38.p7	12:110019108	ATCTTCCCTACTTTG[C/T]ACTTAGTTATGCCTT	88455
rs752642688	snp	C/G	1.64732e-05	0.0028699	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036274	AGGAACTTTCAGGAC[C/G]AGCTTCGAATGGAGG	88455
rs752769050	snp	A/G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021272	ATTGATACCAGCTAC[A/G/T]AAAAGAATATAGCTG	88455
rs752778343	snp	A/C	1.65198e-05	0.00287395	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037389	CCTCCTCACCAGCAC[A/C]GAAGGCCTGTGCCCC	88455
rs752836978	snp	A/G	1.65091e-05	0.00287303	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037427	TGAGCGAGACAAGCC[A/G]TTTTGATAATGACTT	88455
rs752899380	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015378	TTGAATGGATGGAAT[C/T]GACATTCCCTGCCCT	88455
rs752945177	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110005346	GAAAATGTGTCCCTA[C/T]GTTGCCCAGACTGGG	88455
rs752960466	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017032	ACCCACCCTAGCCCC[C/G]CAAAGTGCTGGGATT	88455
rs753007415	snp	C/T	1.66333e-05	0.00288381	intron-variant	ANKRD13A	GRCh38.p7	12:110029679	TGGAGGTTCTGCCCA[C/T]GTTTGTGGGTGGCAG	88455
rs753069809	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036704	GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC	88455
rs753085509	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003886	TTTTTTGGCTGGGCA[C/T]GGTGGCTCACGCCTG	88455
rs753168827	snp	C/T	1.71475e-05	0.00292805	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030701	GGAAATGTTAATGGC[C/T]GTAGCACTGCCGAAG	88455
rs753223119	snp	G/T	3.30235e-05	0.00406333	intron-variant	ANKRD13A	GRCh38.p7	12:110016341	CTGCTTATGTTGTGT[G/T]GATAGTGCCAAGGGT	88455
rs753247338	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023741	ATCTTCAGTCACTTC[C/T]TTGGGACTGCTGTCC	88455
rs753302534	snp	C/T			synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025798	CACAGAACATCTGAC[C/T]GAGGAGGAAAAAAAG	88455
rs753303334	snp	A/G	3.37638e-05	0.00410862	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019318	GATACTAAAAATATT[A/G]CTTTTGAAAGGTACA	88455
rs753487282	in-del	-/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039068	TCACAATCTGTTTTG[-/T]TTTTTTTTTTTTGTC	88455
rs753582820	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, stop-gained	ANKRD13A	GRCh38.p7	12:110036293	TTCGAATGGAGGGAT[C/T]AGCCAGACAAACACC	88455
rs753617095	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110034556	ATCCTCCCACCTCAG[C/T]CTCCCAAGTAGCTGG	88455
rs753745233	snp	C/G	1.68088e-05	0.00289899	intron-variant	ANKRD13A	GRCh38.p7	12:110037331	ATGATAGTAGTGACT[C/G]TCCCTTTTTATCTGT	88455
rs753865327	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007327	TTTTAAACCATGAGC[A/G]TAAGGATGTTTTTCA	88455
rs753874717	snp	C/G	4.94303e-05	0.00497119	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013175	ATGGTGTACACAGTT[C/G]TCCAACATCGAGACT	88455
rs753903377	snp	A/G	3.29554e-05	0.00405914	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028533	ACCACGGAATGTGCT[A/G]CTGCAAACAACCCCA	88455
rs753925358	snp	A/C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028141	GGTACAGTGGATGTC[A/C/T]CTGCGGGTCAGAAAA	88455
rs754000428	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007059	TTCCATTGACCTGTA[-/T]GTCTGTCCTTATGCC	88455
rs754051110	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029015	TGCTGGGATTACAGG[C/G]ATGAGCCACTGCGCC	88455
rs754056190	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013566	TTTGCTGAAGCCCAG[A/G]AGTTTGAGACCAGCC	88455
rs754147288	snp	A/G	5.28881e-05	0.00514211	intron-variant	ANKRD13A	GRCh38.p7	12:110019340	AAAGGTACAAATTTA[A/G]ACTCTAAATTTTAAT	88455
rs754154755	in-del	-/A	1.64988e-05	0.00287213	intron-variant	ANKRD13A	GRCh38.p7	12:110024040	TGGTGTTCACTTTTT[-/A]ATCAGAACTAAATCC	88455
rs754182669	snp	A/G	0.000141854	0.00842062	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999768	ACCGGCAGCTCGAGA[A/G]GGAGCTGCAGGGCCA	88455
rs754184771	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000876	GATTCTTCTGCCTCA[G/T]CCCCCCAAGTAACTG	88455
rs754195736	snp	C/T			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998826	TTTGGGGAGTGCTAC[C/T]GGCATTGAGTGGGGA	88455
rs754368413	snp	C/T	3.30278e-05	0.0040636	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037454	ACTTGCAGCTAGCCA[C/T]GGAGCTCTCTGCCAA	88455
rs754388473	snp	A/G	1.64803e-05	0.00287052	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012037	CCCACGAGGTCGAAC[A/G]TTATTGCATCTTGCT	88455
rs754561857	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110033455	TCAGATATTTTATAT[A/G]TACTTTTATATATTT	88455
rs754566253	snp	C/T	1.66991e-05	0.00288951	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012102	TACTCCGACATAAAG[C/T]AGATGTGACAAAAGA	88455
rs754581293	snp	C/T	2.54891e-05	0.00356986	intron-variant	ANKRD13A	GRCh38.p7	12:110012176	TAAAGTCCGTCTGAG[C/T]ACCATGGTGAAACCC	88455
rs754618114	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034599	GCACCACTGTGCCCA[C/G]TAGAACAGTTGCCTT	88455
rs754667334	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019024	CACTGTAGGTTTTAC[C/T]AGATAGCACCTGGGA	88455
rs754853546	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110020904	AATCTCCAAAGTCTG[-/T]GACTCTTAAGATGTC	88455
rs754866530	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110020493	TGTCCAGGGCTGCTG[C/T]TAGGGCAGGAGGGTG	88455
rs754884382	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006105	TACAGGCATGAGCCA[C/G]TGCACCCAGCCCCAT	88455
rs754940501	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007358	ATTTATTTAGGTCTT[C/G]TTTAATTTTTTGAGG	88455
rs755033810	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110028380	TTTTCTTGTTCCATG[C/G]AAAAAAGTTAGTGAA	88455
rs755086657	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029036	CCACTGCGCCCAGCC[G/T]CCTCTGCCCCTTTTT	88455
rs755127508	snp	A/G	1.65127e-05	0.00287334	intron-variant	ANKRD13A	GRCh38.p7	12:110025826	AAGAGATATAAAGGT[A/G]ATCACCACCACCCTC	88455
rs755163956	snp	A/G	1.65359e-05	0.00287536	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037369	CCCAGGGCCATCCAG[A/G]AGAGCCTCCTCACCA	88455
rs755204008	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110009687	AGATGAGAGAGATGC[A/C]GGAAGGTCTGAAGAG	88455
rs755213799	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110013631	AAAAAATTAGCAGGG[C/T]ATGGTAGTGCATACC	88455
rs755301090	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000916	GGATGCACCACCACG[C/G]CCGGCTAATTTTGTA	88455
rs755373408	snp	C/T	1.65688e-05	0.00287821	intron-variant	ANKRD13A	GRCh38.p7	12:110029663	AAACTTCAGCAACAC[C/T]TGGAGGTTCTGCCCA	88455
rs755382995	in-del	-/A	1.64904e-05	0.00287139	frameshift-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028513	TTCTGGCTCAGCAGG[-/A]CCTCACCACGGAATG	88455
rs755427453	snp	A/C/G	0.000515979	0.0160539	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029561	TTGACCTAATGGCTC[A/C/G]AACGAGTGCTCATTT	88455
rs755439564	snp	A/G			synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037503	GCTCCGGCTCCAGGA[A/G]GAAGAGGCTGAGCTC	88455
rs755461267	snp	G/T	1.64806e-05	0.00287054	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019232	TGGAGCGCCTCACTC[G/T]GGACTTGATGAAGCC	88455
rs755470568	in-del	-/GAGCTCCGGCTCCAGGAGGAAGAGGCT	1.65326e-05	0.00287507	cds-indel	ANKRD13A	GRCh38.p7	12:110037486	GAGCTGGAGGAATGG[-/GAGCTCCGGCTCCAGGAGGAAGAGGCT]GAGCTCCAGCAAGTC	88455
rs755521150	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009286	GGGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTCG	88455
rs755602391	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027917	ATACTCTTTTGGAAG[A/G]GAATTAGATGAGTGA	88455
rs755675608	in-del	-/GA			intron-variant	ANKRD13A	GRCh38.p7	12:110022020	AGGTGAAAATGGCAC[-/GA]GAGAGGGAAGCCAGG	88455
rs755705630	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029565	CCTAATGGCTCGAAC[A/G]AGTGCTCATTTTGCA	88455
rs755714855	snp	A/C			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998316	CACAAATCTTCTGGG[A/C]TCCACATCTGTGGAG	88455
rs755791451	snp	G/T	1.66355e-05	0.002884	intron-variant	ANKRD13A	GRCh38.p7	12:110029680	GGAGGTTCTGCCCAT[G/T]TTTGTGGGTGGCAGC	88455
rs755865090	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110031889	TTTTTTTCTTACACA[A/G]TTGCATGGCCAGGAT	88455
rs755886602	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019845	AAGAATCTGGAGGGG[A/T]TTCAGTTCTGTTCCA	88455
rs755903359	snp	G/T	3.29908e-05	0.00406132	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033834	GGTTGATCAATCTGT[G/T]TTTGAAATTCCCGAA	88455
rs755919632	snp	C/T	1.7988e-05	0.00299895	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033989	ACTCTAATGGCAGGG[C/T]GTGGGAGGTCTTACC	88455
rs755936025	snp	G/T	1.71885e-05	0.00293154	intron-variant	ANKRD13A	GRCh38.p7	12:110024149	AAGATTTAATATAGC[G/T]ATTTAGCTTCTATGC	88455
rs756011134	snp	C/T	4.94189e-05	0.00497062	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036280	TTTCAGGACCAGCTT[C/T]GAATGGAGGGATCAG	88455
rs756012185	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017613	TCTAATGCACATAGT[C/G]ACTCTTATTTCAGGT	88455
rs756099541	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004254	AGTTAAAGGAGGATG[A/G]GTATTTTTATTTGGG	88455
rs756112503	snp	A/G	1.65195e-05	0.00287393	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037393	CTCACCAGCACAGAA[A/G]GCCTGTGCCCCAGCG	88455
rs756141937	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018818	TGCTCACCCAATGTT[G/T]TGCATACATAATTTC	88455
rs756174893	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110013970	AGGGATTTTCAGATT[A/C]TGTTAAGGCTCAGAG	88455
rs756192115	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026775	TAGTCTCAGCTACTG[A/G]GGAGGCTGAGGCAGG	88455
rs756206384	snp	C/T	1.65241e-05	0.00287433	intron-variant	ANKRD13A	GRCh38.p7	12:110027772	TGCACAAGGGGTAAG[C/T]TGAAGCAATGAGCTT	88455
rs756259138	in-del	-/TTCT			intron-variant	ANKRD13A	GRCh38.p7	12:110007685	ACACCAGGCCAGTTC[-/TTCT]TTAATTTTTTTTAAA	88455
rs756264438	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006520	TTGACTTGTTGAGTT[A/G]TAAAGGTTCTTTGCA	88455
rs756271430	snp	C/T	3.30169e-05	0.00406293	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037431	CGAGACAAGCCGTTT[C/T]GATAATGACTTGCAG	88455
rs756289642	snp	C/T	4.94515e-05	0.00497225	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028522	AGCAGGACCTCACCA[C/T]GGAATGTGCTACTGC	88455
rs756383898	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110028020	ATTATAAACGAGGGG[A/C]CTCTTTATAGAAATG	88455
rs756549114	snp	C/G	3.29614e-05	0.00405951	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019239	CCTCACTCTGGACTT[C/G]ATGAAGCCAAAAAGC	88455
rs756557873	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110016281	TCTTCTTATTTTCTC[-/T]TTTTTTTTTTTTTAA	88455
rs756596856	snp	C/T	0.000129107	0.00803349	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999719	GACGCGGGCGACCAC[C/T]ACCCCCTGCACCTCC	88455
rs756605446	snp	C/T	1.73417e-05	0.00294458	intron-variant	ANKRD13A	GRCh38.p7	12:110019332	TGCTTTTGAAAGGTA[C/T]AAATTTAGACTCTAA	88455
rs756605833	snp	C/T			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998831	GGAGTGCTACTGGCA[C/T]TGAGTGGGGAGAAAG	88455
rs756615077	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036457	ACTGGCAGGAAAGAC[C/T]AGAAAAAGTAGGCCA	88455
rs756667243	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000608	GTTGTTGAAAGTGGG[C/G]AGTGGGTGCTTCTGG	88455
rs756738305	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037281	GTGCCCTTGGTAAGC[A/G]GTTAAGAAATGTAGT	88455
rs756796674	snp	A/G	1.72743e-05	0.00293885	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030713	GGCTGTAGCACTGCC[A/G]AAGAATCTGTATCTC	88455
rs756828075	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022079	TGCAAAGTTACCAAG[A/G]GCCACAGAGTTATTA	88455
rs756840160	snp	A/G	1.64923e-05	0.00287156	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019265	AAAGCAGGGAAGTTG[A/G]GCGGCGGCTCACAAG	88455
rs756852738	snp	C/G/T	7.74361e-05	0.00622199	intron-variant	ANKRD13A	GRCh38.p7	12:110030616	TCTCAGTAAAGTTTA[C/G/T]TTATAAAAGTTTTTA	88455
rs756881091	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009243	TGTGCCACCACGCGC[A/G]GCTAATTTTGTATTT	88455
rs756930000	snp	A/G	1.793e-05	0.00299411	intron-variant	ANKRD13A	GRCh38.p7	12:110019348	AAATTTAGACTCTAA[A/G]TTTTAATGTCTAATC	88455
rs757049266	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110025355	AGGGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA	88455
rs757054501	snp	C/T	3.29609e-05	0.00405948	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025797	GCACAGAACATCTGA[C/T]CGAGGAGGAAAAAAA	88455
rs757215170	snp	A/G	3.30033e-05	0.00406209	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027722	GACAGGAACCCGCTG[A/G]AATCTTTGCTGGGAA	88455
rs757233645	snp	G/T	1.65007e-05	0.00287229	intron-variant	ANKRD13A	GRCh38.p7	12:110016355	TTGATAGTGCCAAGG[G/T]TAATCTGTTTTAAAC	88455
rs757331269	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039059	TAATTCCATTTCACA[A/G]TCTGTTTTGTTTTTT	88455
rs757465378	snp	C/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028623	GGAAGGCCGAAAGAG[C/G]TGACGATTAGAACAC	88455
rs757551844	in-del	-/GTT	1.65108e-05	0.00287317	cds-indel, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024089	ACAGATAAAGCAGAA[-/GTT]GTTAATGGTTACGAA	88455
rs757655686	snp	A/C	0.00060241	0.0173448	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999782	AAGGAGCTGCAGGGC[A/C]AGGTGAGGGGCGGGG	88455
rs757745654	snp	A/C	1.64885e-05	0.00287123	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012064	TGCTGTTTCCTTGGG[A/C]CATTTGGAATCTGCT	88455
rs757817681	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110012642	TGGTTACCTCCATTG[A/C]ATCCATCAAAATAGG	88455
rs757933843	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023186	CTGGGATGTGATGTC[C/T]TAGACAAAGGGTAGG	88455
rs757941658	snp	C/G			missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019246	CTGGACTTGATGAAG[C/G]CAAAAAGCAGGGAAG	88455
rs757944253	snp	A/G			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998602	TATTCGCAGACTGTG[A/G]TCAAATATGTATATT	88455
rs757945864	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036365	GGAATAAACCAGGGT[A/G]AACACAGGCCTGGAC	88455
rs757977960	snp	A/G	1.87869e-05	0.00306482	intron-variant	ANKRD13A	GRCh38.p7	12:110019367	TAATGTCTAATCCCC[A/G]TGCTGCCATCTTGAG	88455
rs757983558	snp	A/G	5.1492e-05	0.00507379	intron-variant	ANKRD13A	GRCh38.p7	12:110023969	AGCTGGGGGGGAAAA[A/G]AACTATAAAGGCTAC	88455
rs758058505	snp	C/T	3.31257e-05	0.00406962	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012089	TCTGCTCGAGTCTTA[C/T]TCCGACATAAAGCAG	88455
rs758148271	in-del	-/TTT			intron-variant	ANKRD13A	GRCh38.p7	12:110019788	TTGTTTGTTTGTTTG[-/TTT]GTTTGTTTAACCCAC	88455
rs758326203	snp	A/C	1.64849e-05	0.00287092	intron-variant	ANKRD13A	GRCh38.p7	12:110018341	GTACACTTCTCTCCT[A/C]CAGTGCCCTTGGTTT	88455
rs758347434	in-del	-/CT	1.65968e-05	0.00288065	intron-variant	ANKRD13A	GRCh38.p7	12:110025707	TGGAGTTTTGATTCC[-/CT]GTGTCACTGTTTTCT	88455
rs758371790	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019011	TCGATAATCAGTACA[C/T]TGTAGGTTTTACCAG	88455
rs758389697	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029214	TGAAACTGTTCCACC[C/T]GCTATCATTTCTTCA	88455
rs758412479	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110013744	TGAGGGTGCAGTGAT[C/T]GCACCCCTGCACTCC	88455
rs758536908	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001237	CTGGTTTTTGAATGG[C/T]TCAAAATTGGTGCTA	88455
rs758540766	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110026578	GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	88455
rs758559728	snp	A/G	1.86572e-05	0.00305422	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034002	GGCGTGGGAGGTCTT[A/G]CCCTCTGGGTTAGCC	88455
rs758593632	snp	A/G	3.43365e-05	0.00414332	intron-variant	ANKRD13A	GRCh38.p7	12:110019125	CTTAGTTATGCCTTT[A/G]TTTCCATTAATAGAC	88455
rs758601544	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002638	AAAAAAAACCCAAAA[A/G]ATTCTTATCACCCCA	88455
rs758650747	snp	C/T	1.64738e-05	0.00286995	stop-gained, missense	ANKRD13A	GRCh38.p7	12:110036297	AATGGAGGGATCAGC[C/T]AGACAAACACCTATG	88455
rs758660209	snp	A/C/G	0.000148965	0.00862912	synonymous-codon, missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037500	GGAGCTCCGGCTCCA[A/C/G]GAGGAAGAGGCTGAG	88455
rs758739186	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015794	TTAACTCATCCACCC[A/G]CCTCGGCCTCCCAAA	88455
rs758822760	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038942	TTCTATTGTGCTTCT[C/T]TGGGGATAGGAAGAG	88455
rs758837531	snp	A/G/T	9.62287e-05	0.00693588	intron-variant	ANKRD13A	GRCh38.p7	12:110012169	AATAATTTAAAGTCC[A/G/T]TCTGAGCACCATGGT	88455
rs758913072	snp	A/G	1.64827e-05	0.00287073	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028642	CGATTAGAACACAGA[A/G]GTAAGAGAGGTTCAG	88455
rs758997511	snp	C/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029530	CTCTCTCTGGTGGAG[C/G]AGGTCATTCCCATCA	88455
rs758997709	snp	A/G	1.65048e-05	0.00287265	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018486	TTATATTTAAGGGAG[A/G]AGGTGAGTGACTTCT	88455
rs759029622	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012322	AGTGAACTGTGATTG[C/T]GTCACTGCACTCCAC	88455
rs759158522	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036609	TACAAAAAATTAGCC[A/G]GGCATGGTGCCAGGC	88455
rs759254043	snp	C/T	1.64939e-05	0.0028717	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025747	CACCTCTCAGGTTTA[C/T]ACAGTAAACAATGTG	88455
rs759272699	snp	C/T	1.6669e-05	0.00288691	intron-variant	ANKRD13A	GRCh38.p7	12:110025857	CCACCTCCTGTTTTG[C/T]TGTTATTTTTTAAGC	88455
rs759330023	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000255	TAACTCGCCCTGTGA[C/T]CTTGGGCAAGGCATT	88455
rs759367374	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110021771	ACTTTTTTCTAATCC[A/G]TTACTCAGAGCTTAT	88455
rs759376975	in-del	-/TAA			intron-variant	ANKRD13A	GRCh38.p7	12:110030932	AAACCCTGTCTCTAC[-/TAA]TAATACAAAAATTAG	88455
rs759400191	snp	A/G	4.94564e-05	0.0049725	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019192	AAAGTGGTCACCACC[A/G]AACGCTTCGACCTTT	88455
rs759413867	snp	C/G	1.64928e-05	0.00287161	intron-variant	ANKRD13A	GRCh38.p7	12:110029463	CCTCAGTCTTTTCTT[C/G]GTTGAATTCTGCAGG	88455
rs759449264	in-del	-/C	3.70865e-05	0.00430603	intron-variant	ANKRD13A	GRCh38.p7	12:110019363	ATTTTAATGTCTAAT[-/C]CCCATGCTGCCATCT	88455
rs759452049	snp	A/T	1.74327e-05	0.00295229	intron-variant	ANKRD13A	GRCh38.p7	12:110019104	TTGCATCTTCCCTAC[A/T]TTGCACTTAGTTATG	88455
rs759571730	snp	A/T	0.000252557	0.0112345	intron-variant	ANKRD13A	GRCh38.p7	12:110030802	GTTTTGTTATTTAAA[A/T]AAAAATTTATGGCCG	88455
rs759624318	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022833	AGTGTCAGTTGGAGA[C/T]AGCATTTGGTATAAT	88455
rs759661851	snp	G/T	1.74491e-05	0.00295368	intron-variant	ANKRD13A	GRCh38.p7	12:110023959	CACTAACTTAAGCTG[G/T]GGGGGAAAAAAACTA	88455
rs759700216	snp	A/T	1.66493e-05	0.0028852	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019305	TAACACCAGCCTCGA[A/T]ACTAAAAATATTGCT	88455
rs759706025	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009953	CACTGCAACCTCCGC[C/T]TCCCAGGTTCAAGCG	88455
rs759775857	snp	C/T	8.2494e-05	0.00642185	intron-variant	ANKRD13A	GRCh38.p7	12:110013273	GAAAATGTGGCCAGG[C/T]CATAATCTGAGCTAA	88455
rs759821273	snp	C/G	0.000139597	0.00835337	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999687	GTTACGGCCTCCTCG[C/G]CATGTCCTCGGCCTG	88455
rs759845338	snp	C/G	3.29652e-05	0.00405974	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012023	GTGGAGGCTGTGGAC[C/G]CACGAGGTCGAACAT	88455
rs759969367	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110034393	CTCTCTCTGGGTCTC[C/T]AGTGAAACAGAAAAT	88455
rs760058536	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110005029	AAAAGATTTTTATTG[A/C]GATATAGTTCACTTA	88455
rs760164877	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025218	AAAATTAACCAGTCA[C/T]AGTAGCACATGCCTG	88455
rs760366129	snp	C/G	6.62614e-05	0.00575554	intron-variant	ANKRD13A	GRCh38.p7	12:110027808	GCAGTTAGATGAAAG[C/G]AAACAACTTGTCTGT	88455
rs760473665	snp	A/T			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997841	TTACAAAATGGTGTG[A/T]GATAAACACAATGAA	88455
rs760474352	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012196	TGGTGAAACCCTGTC[C/T]CTACAAAAAAATATG	88455
rs760548890	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035996	GTTGTGTATATCTTC[C/G]ACGTGGGTTAGCTGT	88455
rs760553161	snp	G/T	1.68448e-05	0.00290209	intron-variant	ANKRD13A	GRCh38.p7	12:110037326	TGATGATGATAGTAG[G/T]GACTCTCCCTTTTTA	88455
rs760556091	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110034363	TTCCTCCACAAAGGG[C/T]ACCATCTCCCTAAAC	88455
rs760596699	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:109999956	CGAGTGCTTACCGTG[A/C]GACGGGCTTTTTAAA	88455
rs760659033	in-del	-/A	0.000308103	0.0124079	intron-variant	ANKRD13A	GRCh38.p7	12:110030799	TTAGTTTTGTTATTT[-/A]AAAAAAAATTTATGG	88455
rs760710748	snp	A/G	1.65075e-05	0.00287289	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024085	GAGGACAGATAAAGC[A/G]GAAGTTGTTAATGGT	88455
rs760741860	snp	G/T	1.80364e-05	0.00300298	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037599	GCAGAGGCTGTGGGC[G/T]GTCACAGATGCTGTG	88455
rs760763747	snp	C/G	1.64806e-05	0.00287054	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012032	GTGGACCCACGAGGT[C/G]GAACATTATTGCATC	88455
rs760782937	snp	C/T	2.02059e-05	0.00317845	intron-variant	ANKRD13A	GRCh38.p7	12:110012147	GGACAGGTAAGTATA[C/T]TTTTACAATAATTTA	88455
rs760825839	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028613	CAGGGACATTGGAAG[A/G]CCGAAAGAGCTGACG	88455
rs760893955	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007191	CTAGGTTTCTTGCAT[C/T]TCCACATGAATTCTA	88455
rs760968623	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028955	ATTGGTCAGGCTGGT[C/T]TCGAACTCCTGACCT	88455
rs761074615	snp	A/G	1.71546e-05	0.00292865	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030702	GAAATGTTAATGGCT[A/G]TAGCACTGCCGAAGA	88455
rs761091080	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030314	TGGGATTATAGGCAT[A/G]CATCACCACGCCCAG	88455
rs761168712	snp	C/T	1.7031e-05	0.00291808	intron-variant	ANKRD13A	GRCh38.p7	12:110033771	TGTAATGAACTCAGA[C/T]ACTGGACGGTTGCCT	88455
rs761187272	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023964	ACTTAAGCTGGGGGG[A/G]AAAAAAACTATAAAG	88455
rs761190108	snp	A/G	1.64996e-05	0.0028722	intron-variant	ANKRD13A	GRCh38.p7	12:110018330	TTTTCTCAGTAGTAC[A/G]CTTCTCTCCTCCAGT	88455
rs761243894	in-del	-/TA			intron-variant	ANKRD13A	GRCh38.p7	12:110016951	TAATCTTTGTATTTT[-/TA]TAGTAGAGAGTGGGG	88455
rs761298796	snp	G/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038662	TTAACAATCTTTTTA[G/T]TATTTGTAAAAGATA	88455
rs761323209	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036407	GACGCGTGGCACTGT[G/T]CATTTGGTCCTCAGG	88455
rs761398140	in-del	-/TTTTTTTTTTTTT			intron-variant	ANKRD13A	GRCh38.p7	12:110014789	CTAGCATTTCTCTTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGAG	88455
rs761504636	snp	A/G	9.885e-05	0.0070296	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018443	CTGGGATTTGAAAAC[A/G]TGAGCTGGATAAGAG	88455
rs761557149	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110010187	TGAGTGTTAATCCTT[A/C]CTCTGCGCTTTTAGT	88455
rs761600613	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110024814	GTTGGGGCTCCTCAC[A/G]TGGCATATAGAGAGA	88455
rs761646363	in-del	-/T	1.69306e-05	0.00290947	intron-variant	ANKRD13A	GRCh38.p7	12:110033780	TCAGACACTGGACGG[-/T]TTGCCTTTTGTTTCA	88455
rs761649207	snp	A/T	1.68021e-05	0.0028984	intron-variant	ANKRD13A	GRCh38.p7	12:110037332	TGATAGTAGTGACTC[A/T]CCCTTTTTATCTGTT	88455
rs761660891	snp	A/G	0.000555607	0.0166582	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999651	CCGGGGCCGAGACTT[A/G]GGGCGGGCGACGAGG	88455
rs761738913	snp	A/G	1.65165e-05	0.00287367	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037417	CCCAGCGCCCTGAGC[A/G]AGACAAGCCGTTTTG	88455
rs761750219	in-del	-/TCTT			intron-variant	ANKRD13A	GRCh38.p7	12:110025963	TCTTCTCTCTCTCTC[-/TCTT]TTTTTTTTTTTTTGA	88455
rs761917687	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110020194	CCTGAGAAAATGGAC[A/G]CTATTATCCTTATAG	88455
rs761920372	snp	A/G			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034216	ATATTCACGCACATA[A/G]CTTGTAATTCTGTAC	88455
rs761930067	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025088	AGGCTGGGTGCAGTG[G/T]CTCACGCCTGTAATC	88455
rs761958095	in-del	-/GTC			cds-indel, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018381	GCCCAAATGATGTCT[-/GTC]GCATCTGGAAAAGTG	88455
rs762042694	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006968	GACAGTTCTTTCCCA[A/G]TGAATTATTTTGGCA	88455
rs762045190	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035871	AGTGAGCTACGATCA[C/T]ATCACTACCCTTGAG	88455
rs762064762	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110005743	TTCTCCGTTTGTCAG[C/T]TGATGGACATTTGGG	88455
rs762126665	snp	A/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029488	TGCAGGTTTAAAGCA[A/T]TGTTGTGGATGTGTG	88455
rs762137783	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022274	CTAACACGGTGAAAC[C/G]CCATATCTACTAAAA	88455
rs762151064	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110027894	ATACCCCCAAGCTGG[A/C]ATTTGAGATACTCTT	88455
rs762182883	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110010777	TTCGCAAAACAGGGA[A/G]GTTTGATAGCTATTG	88455
rs762295453	snp	A/G	1.66015e-05	0.00288105	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024104	GTTGTTAATGGTTAC[A/G]AAGCAAAGGTAAAAG	88455
rs762310081	snp	C/G	2.31078e-05	0.00339902	intron-variant	ANKRD13A	GRCh38.p7	12:110012165	TTACAATAATTTAAA[C/G]TCCGTCTGAGCACCA	88455
rs762314023	snp	A/C	1.65682e-05	0.00287817	intron-variant	ANKRD13A	GRCh38.p7	12:110025722	CTGTGTCACTGTTTT[A/C]TTTCGCATACACCTC	88455
rs762332886	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029999	CCAAGATCCTTTGAT[A/T]TGTAAATATGATCTA	88455
rs762362697	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028894	AGGCGCGTGCCACCA[C/T]GCCCAGCTAATTTTT	88455
rs762513104	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110013305	TGCTGATACAATTAC[G/T]GGAGACACAGTTTGA	88455
rs762568204	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015072	TGAGCCAGTGCGCCC[A/G]GCCGCATTTCTCTTC	88455
rs762617262	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110037195	GTGGGGTTTCTCACC[C/T]GTATACAACACCTAC	88455
rs762672750	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022051	TGTTCTATCATCTTC[A/G]GATGCTTTTGCATGC	88455
rs762687653	snp	C/T	3.37661e-05	0.00410876	intron-variant	ANKRD13A	GRCh38.p7	12:110024126	AGGTAAAAGGAAACT[C/T]TTAAAATAAGATTTA	88455
rs762714909	snp	C/G	1.6473e-05	0.00286988	intron-variant	ANKRD13A	GRCh38.p7	12:110036252	GTCTATCACATTTGT[C/G]TTTGCCAGGAACTTT	88455
rs762752533	snp	A/G			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997550	TTTACATTTTTAAAG[A/G]GTTGCGAGATGAAAA	88455
rs762769885	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110010018	AATATAGGCACTCAC[A/C]ACCTCGCCTGGCTAA	88455
rs762783172	snp	C/T	1.6525e-05	0.00287441	intron-variant	ANKRD13A	GRCh38.p7	12:110028491	TGGCATTTCTGACTC[C/T]CCTGAGTTCTGGCTC	88455
rs762851599	snp	A/G	1.72838e-05	0.00293966	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037569	GACCTTTCAGCCTGT[A/G]AGCCTCTGCACAAAG	88455
rs762873412	snp	A/G	3.29468e-05	0.00405861	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028596	GAGTTTGATCTGAAA[A/G]ACAGGGACATTGGAA	88455
rs762887689	snp	A/C/T	6.60506e-05	0.00574644	intron-variant	ANKRD13A	GRCh38.p7	12:110029448	ATCTGGTGGAGATGA[A/C/T]CTCAGTCTTTTCTTG	88455
rs763064975	snp	A/C			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034114	GCATCTGGTCTTCTT[A/C]CAAAAGCTTGTTATG	88455
rs763112436	in-del	-/CAGA	3.29462e-05	0.00405857	frameshift-variant	ANKRD13A	GRCh38.p7	12:110036297	AATGGAGGGATCAGC[-/CAGA]CAAACACCTATGACG	88455
rs763135045	snp	A/G	1.65132e-05	0.00287339	intron-variant	ANKRD13A	GRCh38.p7	12:110029641	GTCAAAATAGGTACT[A/G]CTAAATAAACTTCAG	88455
rs763161655	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032731	ATGCGCTATTGTGCT[C/T]TATTAATACAACAGA	88455
rs763217473	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017165	TCCAACTGCCCCAGC[C/T]CCCCAAATTGCTGGG	88455
rs763255679	snp	C/T	3.29582e-05	0.00405931	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019222	TCCCAAGAAATGGAG[C/T]GCCTCACTCTGGACT	88455
rs763280451	snp	C/T	1.6549e-05	0.0028765	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019293	AAGCCCTGTCATTAA[C/T]ACCAGCCTCGATACT	88455
rs763324097	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110005582	TAAATAGAATCATAT[C/G]TGGCCTTTTGTTTCT	88455
rs763355622	snp	C/T	1.64849e-05	0.00287092	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013150	GGCTGTGAGCACTGG[C/T]GATCCTGAGATGGTG	88455
rs763448404	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110006918	TGTTCTTTTGCATGT[A/T]GATATGCAGTTGTTC	88455
rs763581798	snp	A/C	1.65693e-05	0.00287826	intron-variant	ANKRD13A	GRCh38.p7	12:110027813	TAGATGAAAGGAAAC[A/C]ACTTGTCTGTGTCTG	88455
rs763641706	snp	C/T	3.30006e-05	0.00406192	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027717	TAGCAGACAGGAACC[C/T]GCTGGAATCTTTGCT	88455
rs763697229	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037198	GGGTTTCTCACCCGT[A/G]TACAACACCTACACC	88455
rs763767103	snp	C/T	1.65119e-05	0.00287327	intron-variant	ANKRD13A	GRCh38.p7	12:110016340	CCTGCTTATGTTGTG[C/T]TGATAGTGCCAAGGG	88455
rs763783592	snp	C/T	3.30376e-05	0.0040642	intron-variant	ANKRD13A	GRCh38.p7	12:110018317	TTGGCCCTTGAGTTT[C/T]TCTCAGTAGTACACT	88455
rs763784739	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019790	TTTGTTTGTTTGTTT[-/T]GTTTGTTTAACCCAC	88455
rs763794180	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009166	GGCTCACCACAACCT[C/T]CGCCTTCCGGGTTCA	88455
rs763873002	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023151	AGTCAGGCTGTTGCC[A/G]TAGCCAGGGCCAAGA	88455
rs763901109	snp	C/T	4.9436e-05	0.00497148	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025781	GTGATCACCAAAATA[C/T]GCACAGAACATCTGA	88455
rs763951887	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019206	CGAACGCTTCGACCT[C/T]TCCCAAGAAATGGAG	88455
rs763961724	in-del	-/A	0.000327445	0.0127912	intron-variant	ANKRD13A	GRCh38.p7	12:110023964	CTTAAGCTGGGGGGG[-/A]AAAAAAACTATAAAG	88455
rs764000390	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110010020	TATAGGCACTCACCA[A/C]CTCGCCTGGCTAATT	88455
rs764177604	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017333	GATGAGGTGAATATT[A/G]GAATAGCTTATTTTT	88455
rs764264544	snp	A/G	1.65097e-05	0.00287308	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037439	GCCGTTTTGATAATG[A/G]CTTGCAGCTAGCCAT	88455
rs764280908	snp	C/G	1.81793e-05	0.00301485	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037606	CTGTGGGCTGTCACA[C/G]ATGCTGTGTCAACCA	88455
rs764306965	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003918	ACTCCCAGCTCTTTG[C/G]GAGGCCAAGGCAGGT	88455
rs764334581	snp	C/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028615	GGGACATTGGAAGGC[C/T]GAAAGAGCTGACGAT	88455
rs764383276	snp	A/G	0.000675214	0.0183617	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018413	GGTGCCAAACTGCGC[A/G]TCGATATCACATTGC	88455
rs764431423	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110005592	CATATGTGGCCTTTT[A/G]TTTCTTCTTTTACTT	88455
rs764443717	snp	A/G	5.27329e-05	0.00513456	intron-variant	ANKRD13A	GRCh38.p7	12:110019339	GAAAGGTACAAATTT[A/G]GACTCTAAATTTTAA	88455
rs764449891	snp	C/T	1.70026e-05	0.00291565	intron-variant	ANKRD13A	GRCh38.p7	12:110033773	TAATGAACTCAGACA[C/T]TGGACGGTTGCCTTT	88455
rs764465672	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110005763	GGACATTTGGGTTGT[C/T]GCCACTTTTTGGCTA	88455
rs764658863	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026113	ATTACAAGCACCCAC[C/G]ACCACGCCCGGCTAA	88455
rs764720723	snp	A/G	1.64757e-05	0.00287012	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018445	GGGATTTGAAAACAT[A/G]AGCTGGATAAGAGGG	88455
rs764757402	snp	A/T	1.67396e-05	0.00289301	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033798	GCCTTTTGTTTCAGC[A/T]TCCCACATCACAAAC	88455
rs764773046	snp	C/T	4.94654e-05	0.00497295	intron-variant	ANKRD13A	GRCh38.p7	12:110018338	GTAGTACACTTCTCT[C/T]CTCCAGTGCCCTTGG	88455
rs764840577	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012333	ATTGCGTCACTGCAC[A/T]CCACCCTGGGCAATA	88455
rs764892120	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013244	CTGCTCCAAAAAATT[C/T]TCGAGGTATCCATGA	88455
rs764906967	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110020515	AGGAGGGTGGCATCC[C/T]TGGAGGCAGGGTCAG	88455
rs764986602	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037089	TGTCTATGAGAGCCT[A/G]TTGATGAAGAACCTG	88455
rs765006939	snp	C/T	0.000116437	0.00762921	intron-variant	ANKRD13A	GRCh38.p7	12:110037351	TTTTTATCTGTTTTC[C/T]AACCCAGGGCCATCC	88455
rs765021175	snp	G/T	1.65034e-05	0.00287253	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027727	GAACCCGCTGGAATC[G/T]TTGCTGGGAACTGTG	88455
rs765023435	snp	A/G	1.65149e-05	0.00287353	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037418	CCAGCGCCCTGAGCG[A/G]GACAAGCCGTTTTGA	88455
rs765113049	snp	C/T	1.65748e-05	0.00287874	intron-variant	ANKRD13A	GRCh38.p7	12:110028461	TGCCACAGGCCTTCA[C/T]TTGTGAACATCATTT	88455
rs765175422	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021804	GTGCAAATTAATACC[C/T]TGCCCTGATGAATTT	88455
rs765221833	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009957	GCAACCTCCGCCTCC[C/G]AGGTTCAAGCGATTC	88455
rs765293685	in-del	-/CT	3.36706e-05	0.00410295	intron-variant	ANKRD13A	GRCh38.p7	12:110024124	AAAGGTAAAAGGAAA[-/CT]CTTAAAATAAGATTT	88455
rs765336302	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110030921	CCAACATGGAGAAAC[A/C]CTGTCTCTACTAATA	88455
rs765416553	snp	C/T	3.29468e-05	0.00405861	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029513	TGTGTGAAGAGTTTC[C/T]CCTCTCTCTGGTGGA	88455
rs765457198	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015706	CGTGTGCCACCATGC[C/T]GAGCTAATTTTTGTA	88455
rs765504642	in-del	-/T	8.26453e-05	0.00642774	frameshift-variant, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033823	CAAACTTTGAGGTTG[-/T]ATCAATCTGTGTTTG	88455
rs765507638	snp	C/G	1.64895e-05	0.00287132	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029626	CCACCTGGATTTCCT[C/G]TCAAAATAGGTACTG	88455
rs765560107	in-del	-/GA			intron-variant	ANKRD13A	GRCh38.p7	12:110034458	TGTGTGTGTGTGTGT[-/GA]GACTCTATGTTGCCC	88455
rs765562002	in-del	-/TTC			intron-variant	ANKRD13A	GRCh38.p7	12:110007682	ACCACACCAGGCCAG[-/TTC]TTCTTTAATTTTTTT	88455
rs765577910	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002570	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	88455
rs765579561	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017027	GATCCACCCACCCTA[A/G]CCCCCCAAAGTGCTG	88455
rs765615697	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033885	TGGCAGAAATGTGCA[C/T]TTGCAAGATGAAGAT	88455
rs765655300	snp	C/T	1.65149e-05	0.00287353	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012074	TTGGGACATTTGGAA[C/T]CTGCTCGAGTCTTAC	88455
rs765701571	snp	A/T	1.66927e-05	0.00288895	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024111	ATGGTTACGAAGCAA[A/T]GGTAAAAGGAAACTC	88455
rs765722224	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023685	CCAGATAAATGCTCT[A/G]ACCTGGTTACCACCT	88455
rs765768433	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038782	CTCTTTTGTCAAACC[C/T]TCTTGTATATAACCA	88455
rs765906228	snp	A/G	1.69617e-05	0.00291214	intron-variant	ANKRD13A	GRCh38.p7	12:110024132	AAGGAAACTCTTAAA[A/G]TAAGATTTAATATAG	88455
rs765998597	snp	A/G	1.64871e-05	0.00287111	missense, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033907	GATGAAGATTACGAG[A/G]TAATGCAGTTTGCCA	88455
rs766004570	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011395	CTTGCCTATTTCTTT[C/G]TGAGTAGATCCGCAT	88455
rs766061606	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034503	TGGCTGTTCCCCGGC[A/G]TGATCATATTGCACC	88455
rs766069921	snp	A/C	1.73839e-05	0.00294816	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037573	TTTCAGCCTGTGAGC[A/C]TCTGCACAAAGCAGA	88455
rs766079381	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027203	GAAATTACTTCTGCT[C/G]TGTGCCTTAGTTCCT	88455
rs766085780	snp	G/T	1.6473e-05	0.00286988	intron-variant	ANKRD13A	GRCh38.p7	12:110036253	TCTATCACATTTGTC[G/T]TTGCCAGGAACTTTC	88455
rs766134618	snp	C/T			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034152	CCATCTACATAATCC[C/T]AGTCAGCACCATTCA	88455
rs766144581	snp	A/T			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997893	GAGAAAGGAGATGTG[A/T]CCCTAATACCAATGA	88455
rs766148522	snp	C/G	1.65067e-05	0.00287282	intron-variant	ANKRD13A	GRCh38.p7	12:110028500	TGACTCTCCTGAGTT[C/G]TGGCTCAGCAGGACC	88455
rs766165024	snp	C/T	3.29636e-05	0.00405964	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018345	ACTTCTCTCCTCCAG[C/T]GCCCTTGGTTTCTAG	88455
rs766166768	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028600	TTGATCTGAAAGACA[A/G]GGACATTGGAAGGCC	88455
rs766253422	snp	A/G	6.59304e-05	0.00574116	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018465	GGATAAGAGGGAGGC[A/G]TAGTTTTATATTTAA	88455
rs766303708	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019863	CAGTTCTGTTCCAGA[C/G]TCATAAAGAATTCTC	88455
rs766349615	snp	A/G	1.65222e-05	0.00287417	intron-variant	ANKRD13A	GRCh38.p7	12:110029644	AAAATAGGTACTGCT[A/G]AATAAACTTCAGCAA	88455
rs766559827	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007264	GATAGGAGTTGAATT[A/G]AATCTATACCTCAGT	88455
rs766570220	snp	A/T	1.648e-05	0.0028705	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019228	GAAATGGAGCGCCTC[A/T]CTCTGGACTTGATGA	88455
rs766643944	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029704	TGGCAGCATGTGGGT[-/G]GCAGGATGCTTCAGG	88455
rs766659939	snp	C/T	3.32392e-05	0.00407658	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019302	CATTAACACCAGCCT[C/T]GATACTAAAAATATT	88455
rs766732990	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013471	TTACCCTTTTAAGTA[C/G]TATTTAAAAATTATA	88455
rs766743314	snp	C/T	4.95806e-05	0.00497874	intron-variant	ANKRD13A	GRCh38.p7	12:110025732	GTTTTCTTTCGCATA[C/T]ACCTCTCAGGTTTAC	88455
rs766746709	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015173	AACAGGGCTGCTGTG[A/G]TAGTTTAAAACTTCA	88455
rs766798135	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002339	AAAATTCTTAAGTCC[A/G]GGCACGGTGGCTCAT	88455
rs766832970	snp	A/G	6.59304e-05	0.00574116	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013152	CTGTGAGCACTGGCG[A/G]TCCTGAGATGGTGTA	88455
rs766838714	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029885	TGGTGCTGACAGATA[C/T]AAAAAGGCATAAAAA	88455
rs766870223	snp	G/T	3.29451e-05	0.00405851	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029533	TCTCTGGTGGAGCAG[G/T]TCATTCCCATCATTG	88455
rs766888748	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015954	CTTGTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTC	88455
rs766911299	snp	C/T			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998025	TGGTAAGCAAAACGA[C/T]GTGGTTCCTGTCATT	88455
rs767027625	snp	A/C			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038723	GGTTATACATTTTAA[A/C]CAGATTTTCTCAGGC	88455
rs767035666	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033699	TTGATTGTTATAATT[G/T]TGAGCCTTTCTTTTT	88455
rs767037810	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003683	ATTCACCTGAGGCTA[C/G]TGGGCAAGCTGGAAG	88455
rs767039693	snp	A/G	1.64732e-05	0.0028699	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036271	GCCAGGAACTTTCAG[A/G]ACCAGCTTCGAATGG	88455
rs767040418	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029215	GAAACTGTTCCACCC[A/G]CTATCATTTCTTCAT	88455
rs767135350	snp	A/T	1.6492e-05	0.00287154	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025748	ACCTCTCAGGTTTAC[A/T]CAGTAAACAATGTGA	88455
rs767156220	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110023616	TTCCTCGAGTGAGAT[G/T]TGGCTACTTGTGGAG	88455
rs767169448	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010231	GTGAATTGTAGTAAG[C/T]AGTTTCCCCTTTCCC	88455
rs767197481	snp	C/T	1.64852e-05	0.00287094	intron-variant	ANKRD13A	GRCh38.p7	12:110029475	CTTGGTTGAATTCTG[C/T]AGGTTTAAAGCAATG	88455
rs767227091	snp	A/T	1.64784e-05	0.00287035	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013167	ATCCTGAGATGGTGT[A/T]CACAGTTCTCCAACA	88455
rs767227188	snp	C/G	1.66921e-05	0.00288891	intron-variant	ANKRD13A	GRCh38.p7	12:110025859	ACCTCCTGTTTTGTT[C/G]TTATTTTTTAAGCCT	88455
rs767285571	snp	A/T	1.74251e-05	0.00295165	intron-variant	ANKRD13A	GRCh38.p7	12:110019106	GCATCTTCCCTACTT[A/T]GCACTTAGTTATGCC	88455
rs767312073	in-del	-/CTTT			intron-variant	ANKRD13A	GRCh38.p7	12:110033705	GTTATAATTTTGAGC[-/CTTT]CTTTTTTTTCTAATG	88455
rs767317833	snp	A/T	1.64876e-05	0.00287116	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018471	GAGGGAGGCGTAGTT[A/T]TATATTTAAGGGAGA	88455
rs767503409	in-del	-/G	0.00970784	0.0689904	intron-variant	ANKRD13A	GRCh38.p7	12:110023957	TCACTAACTTAAGCT[-/G]GGGGGGGAAAAAAAC	88455
rs767543125	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110005749	GTTTGTCAGTTGATG[C/G]ACATTTGGGTTGTCG	88455
rs767698077	snp	A/G/T	5.16181e-05	0.00508004	intron-variant	ANKRD13A	GRCh38.p7	12:110023963	AACTTAAGCTGGGGG[A/G/T]GAAAAAAACTATAAA	88455
rs767783859	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007019	ACCATAAATGTGTGG[G/T]TTTATTTCTGGACTC	88455
rs767866352	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110028895	GGCGCGTGCCACCAC[A/G]CCCAGCTAATTTTTG	88455
rs767896607	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110028014	TTATCCATTATAAAC[A/G]AGGGGCCTCTTTATA	88455
rs767937571	snp	A/T	1.65855e-05	0.00287967	intron-variant	ANKRD13A	GRCh38.p7	12:110029670	AGCAACACTTGGAGG[A/T]TCTGCCCATGTTTGT	88455
rs767967381	snp	G/T	1.71369e-05	0.00292714	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030699	TTGGAAATGTTAATG[G/T]CTGTAGCACTGCCGA	88455
rs768088439	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110012645	TTACCTCCATTGAAT[A/C]CATCAAAATAGGCAA	88455
rs768224905	snp	C/T	3.31499e-05	0.0040711	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037512	CCAGGAGGAAGAGGC[C/T]GAGCTCCAGCAAGTC	88455
rs768225979	snp	A/G	1.65138e-05	0.00287343	intron-variant	ANKRD13A	GRCh38.p7	12:110028674	TGCCATTTTCAACCT[A/G]TGTATGTTTCAGAAA	88455
rs768264922	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110010448	CGTCTTGTTACTTTT[-/A]AAAAAAATATTTAAT	88455
rs768387377	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018424	GCGCGTCGATATCAC[A/G]TTGCTGGGATTTGAA	88455
rs768453972	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003169	AGGTGAGTCAGTGTA[C/T]CTTAGACAGGGTTGG	88455
rs768490395	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024505	TTAAATCAGCTTAAT[C/T]GTAATCAGCAGGCGC	88455
rs768495727	snp	A/G			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039631	ATGGCAACTAAAAGC[A/G]AGCCAGTGTTGGGCT	88455
rs768541474	snp	C/T	2.07933e-05	0.00322431	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030648	TTTGTTTGTTAGAAA[C/T]TCCCTTGTTTCATGT	88455
rs768611709	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010920	CAAAATAAAGCACAT[A/T]TTCTAAGATGTATTA	88455
rs768631281	snp	C/T	3.30207e-05	0.00406316	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019282	CGGCGGCTCACAAGC[C/T]CTGTCATTAACACCA	88455
rs768631663	snp	A/G	2.22235e-05	0.00333335	splice-donor-variant, intron-variant	ANKRD13A	GRCh38.p7	12:110030759	CCCAGGCTGATTCAG[A/G]TAAAAAAATAAATAA	88455
rs768641494	in-del	-/A	0.000308103	0.0124079	intron-variant	ANKRD13A	GRCh38.p7	12:110030798	TTAGTTTTGTTATTT[-/A]AAAAAAAAATTTATG	88455
rs768655939	snp	A/G	0.000139266	0.00834348	intron-variant	ANKRD13A	GRCh38.p7	12:110021085	CGAGGACTAAGGCAC[A/G]TTTTGTATTTTTGTG	88455
rs768695357	snp	A/C/T	4.94208e-05	0.00497075	intron-variant	ANKRD13A	GRCh38.p7	12:110036221	ATGGCACCAATTTCT[A/C/T]CTAAGACGTATTCAT	88455
rs768707616	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110011939	TACTTGAAATATCTG[C/T]CAAGCACATTTCCCT	88455
rs768782038	snp	C/G			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998943	AGAAATCATGAAGTA[C/G]AAATATCCCCTTTTA	88455
rs768890612	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019992	GCTGTCAAAGCTGTT[C/T]GCTTGTTTCTACAGT	88455
rs768945364	snp	C/T	1.64762e-05	0.00287016	stop-gained, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013184	ACAGTTCTCCAACAT[C/T]GAGACTACCACAACA	88455
rs768951858	snp	A/C	1.65542e-05	0.00287695	intron-variant	ANKRD13A	GRCh38.p7	12:110018515	CTCTTGTAGTAATCA[A/C]TGCTCAAGCAAAATT	88455
rs768954622	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022230	TGAGGCGGGTGGATC[A/G]CGAGGTCGGGAGATC	88455
rs768978489	in-del	-/CAA			intron-variant	ANKRD13A	GRCh38.p7	12:110025355	AGGGAGACTCTGTCT[-/CAA]AAAAAAAAAAAAAAA	88455
rs769106644	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110020971	TAGAGTTGCCAGAGT[C/G]ATTGTTTGTTGAAGT	88455
rs769269891	snp	C/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028584	TACTTCAATGAAGAG[C/T]TTGATCTGAAAGACA	88455
rs769359726	snp	C/T	1.65285e-05	0.00287471	intron-variant	ANKRD13A	GRCh38.p7	12:110028681	TTCAACCTATGTATG[C/T]TTCAGAAATTGTGCT	88455
rs769427800	snp	A/G	3.3151e-05	0.00407117	intron-variant	ANKRD13A	GRCh38.p7	12:110018526	ATCACTGCTCAAGCA[A/G]AATTACAGGGTGATT	88455
rs769481789	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029851	CAAGAGATCTCCAAC[C/G]ATCATTTCTATTTGC	88455
rs769602623	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110014406	GACAGAGCGAGACTC[A/C]ATCTCAAAAAATAAA	88455
rs769626849	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022864	ACTTTTAGGATTCCT[C/G]TGTTTCCATCCACGG	88455
rs769656229	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110016180	TCTCAAACTCCTGAG[C/T]GCAAGTGATCACCCG	88455
rs769677196	snp	C/T	1.6679e-05	0.00288777	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037540	GTCTTACAGCTGTCA[C/T]TCACTGACAAATAGA	88455
rs769767202	snp	C/T	0.000182226	0.00954358	intron-variant	ANKRD13A	GRCh38.p7	12:110024016	GGCATATTGTACATG[C/T]AGAAATTTGTGGTGT	88455
rs769771483	snp	A/G	1.65135e-05	0.00287341	intron-variant	ANKRD13A	GRCh38.p7	12:110011990	ATTATGTAAATGCCA[A/G]TGTTTCCTTCACAGA	88455
rs769790065	snp	A/C/T	0.000121323	0.0077877	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012122	GTGACAAAAGAAAAT[A/C/T]GCCAGGGATGGACAG	88455
rs769884391	snp	C/T	1.65488e-05	0.00287647	intron-variant	ANKRD13A	GRCh38.p7	12:110025837	AGGTAATCACCACCA[C/T]CCTCCCACCTCCTGT	88455
rs769908812	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024220	CATGGAGATGCTCTG[G/T]GGAATGAGAACTGTC	88455
rs769945860	in-del	-/GAG			intron-variant	ANKRD13A	GRCh38.p7	12:110028014	TTATCCATTATAAAC[-/GAG]GGGCCTCTTTATAGA	88455
rs769958078	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110010848	AGTGGCACTTTCTGC[A/G]TATCTTCAGAGACTG	88455
rs770081408	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027864	GAACAGCCCACTCTA[-/G]TGTAAAGGCCAAAGA	88455
rs770195983	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018285	AGAATCCTGATTTCC[C/T]GGCCTAGGTATTCTT	88455
rs770243907	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035312	TCTAATCTTGCCCTA[C/G]AAGAATTACTGGCTG	88455
rs770284838	snp	A/G	1.64738e-05	0.00286995	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110036328	ACGCCCAGTATGAGA[A/G]GTGATTGACTGACGT	88455
rs770313128	snp	C/T	3.29451e-05	0.00405851	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029572	GCTCGAACGAGTGCT[C/T]ATTTTGCAAGACTGA	88455
rs770316828	snp	A/C	1.65045e-05	0.00287263	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013131	GTTTTCTAGTTTTAC[A/C]TGAGGCTGTGAGCAC	88455
rs770320688	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019656	GTTTATGGATCCACA[A/T]TACTCAGTCCCAGAC	88455
rs770363320	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110024137	AACTCTTAAAATAAG[A/G]TTTAATATAGCTATT	88455
rs770394460	snp	A/C	1.7483e-05	0.00295655	intron-variant	ANKRD13A	GRCh38.p7	12:110019098	TTGTTTTTGCATCTT[A/C]CCTACTTTGCACTTA	88455
rs770465848	in-del	-/C	1.64754e-05	0.00287009	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013195	ACATCGAGACTACCA[-/C]AACACATCCATGGCC	88455
rs770541143	in-del	-/TC			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039060	AATTCCATTTCACAA[-/TC]TGTTTTGTTTTTTTT	88455
rs770555876	in-del	-/GAGAT	1.65206e-05	0.00287403	intron-variant	ANKRD13A	GRCh38.p7	12:110029441	TTTTCCCATCTGGTG[-/GAGAT]GACCTCAGTCTTTTC	88455
rs770674748	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110013936	TTAGGAAAGTTGTGA[C/T]AGGTATCACTTACTA	88455
rs770757756	in-del	-/CAG			intron-variant	ANKRD13A	GRCh38.p7	12:110024511	CAGCTTAATTGTAAT[-/CAG]CAGGCGCACAGCCCA	88455
rs770804116	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000106	TAAATGCCAAGTCGG[C/G]ATTTTAACTCGGGCC	88455
rs770812329	snp	C/G	1.67674e-05	0.00289541	intron-variant	ANKRD13A	GRCh38.p7	12:110013086	TTTTGGAATTTGTCA[C/G]AAAGTATGAGAATTA	88455
rs770837475	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029720	GCAGGATGCTTCAGG[A/G]AATTGGAGTGCTTTA	88455
rs770933395	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009736	TGTGTGCTGCTCTGT[G/T]GCTTATCCATAGGTG	88455
rs771003801	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000352	ACTTGACTCTATTGA[C/T]AGGTCTGGGGTGAGG	88455
rs771010011	snp	C/T	3.61422e-05	0.00425086	intron-variant	ANKRD13A	GRCh38.p7	12:110030784	AAATAAATACAAAGT[C/T]TAGTTTTGTTATTTA	88455
rs771037244	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037894	AGATAAATTTTTATC[A/G]AGGAGTGATAACAAG	88455
rs771127417	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021590	TCCATCATGCCCAGC[C/T]AATTTTTGTATTTTT	88455
rs771263612	snp	G/T	1.66324e-05	0.00288374	intron-variant	ANKRD13A	GRCh38.p7	12:110025850	CACCCTCCCACCTCC[G/T]GTTTTGTTGTTATTT	88455
rs771282112	snp	A/G	3.29853e-05	0.00406098	intron-variant	ANKRD13A	GRCh38.p7	12:110013267	ATCCATGAAAATGTG[A/G]CCAGGCCATAATCTG	88455
rs771368763	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110010583	TTGGGAAGAGTCAGG[A/G]AATCATGGGAGGTGT	88455
rs771430777	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110033628	AAAGAAAAAAGCTGT[A/G]TTCTGTCACTTTTTT	88455
rs771435129	in-del	-/TGTGGGTGGCAGCA	3.32621e-05	0.00407798	intron-variant	ANKRD13A	GRCh38.p7	12:110029682	GGTTCTGCCCATGTT[-/TGTGGGTGGCAGCA]TGTGGGTGGCAGCAT	88455
rs771467743	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018126	AATACTCTTGGGAAA[C/T]TTATTTAGACTTTTT	88455
rs771484562	snp	C/G	1.68729e-05	0.00290451	intron-variant	ANKRD13A	GRCh38.p7	12:110037315	TGCTGCCACCATGAT[C/G]ATGATAGTAGTGACT	88455
rs771489251	snp	C/G	1.65151e-05	0.00287355	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037406	AAGGCCTGTGCCCCA[C/G]CGCCCTGAGCGAGAC	88455
rs771497155	snp	C/T	3.29576e-05	0.00405928	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016425	TGAAATGGGAATTCA[C/T]CAGCTGGGGTGAGTG	88455
rs771706653	snp	A/G	1.65754e-05	0.00287879	intron-variant	ANKRD13A	GRCh38.p7	12:110011955	CAAGCACATTTCCCT[A/G]TTTTAATGTAATACA	88455
rs771811225	snp	A/C			missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028542	TGTGCTACTGCAAAC[A/C]ACCCCACAGCCATCA	88455
rs771850367	snp	A/C	3.53226e-05	0.00420239	intron-variant	ANKRD13A	GRCh38.p7	12:110030623	AAAGTTTACTTATAA[A/C]AGTTTTTATTTTGTT	88455
rs771891766	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110027130	GTCCAAGCAAAAACA[C/T]TGCATGTGGTTGCCA	88455
rs771938067	snp	C/T	1.64955e-05	0.00287184	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019270	AGGGAAGTTGAGCGG[C/T]GGCTCACAAGCCCTG	88455
rs771973057	snp	C/T			splice-donor-variant	ANKRD13A	GRCh38.p7	12:110036330	GCCCAGTATGAGAGG[C/T]GATTGACTGACGTGA	88455
rs771973183	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029600	TGAGAGATTTCATCA[A/G]ATTGGAATTCCCACC	88455
rs771991859	snp	A/G	1.64819e-05	0.00287066	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019196	TGGTCACCACCGAAC[A/G]CTTCGACCTTTCCCA	88455
rs772023665	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012981	AAGAGCTAGCAATCA[A/G]AAGTCATGATCATCC	88455
rs772113550	snp	A/T	1.76256e-05	0.00296859	intron-variant	ANKRD13A	GRCh38.p7	12:110030804	TTTGTTATTTAAAAA[A/T]AAATTTATGGCCGGA	88455
rs772124154	snp	C/T	9.89593e-05	0.00703348	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024055	TATCAGAACTAAATC[C/T]GGATTCTGGGGCTGG	88455
rs772128277	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028214	CTAGAACTTCAACTC[C/T]AAGTCTTCCAAGTCT	88455
rs772210093	snp	A/G	3.57865e-05	0.00422989	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012128	AAAGAAAATCGCCAG[A/G]GATGGACAGGTAAGT	88455
rs772243835	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035903	CTGGACAACAGAGTG[C/T]GACCCTGTCTCTAAA	88455
rs772308323	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008481	TGTGACGCATTTGTC[A/G]TCAGGATAATAGTGG	88455
rs772368186	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036611	CAAAAAATTAGCCGG[G/T]CATGGTGCCAGGCAC	88455
rs772373765	snp	G/T	1.6601e-05	0.00288101	intron-variant	ANKRD13A	GRCh38.p7	12:110025692	TGCTGTGCTTACTTT[G/T]GGAGTTTTGATTCCC	88455
rs772426699	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110021224	AAATGTGTGCTTGTC[A/G]TGCATTGAGCAAGAA	88455
rs772536621	snp	A/G	1.65457e-05	0.00287621	intron-variant	ANKRD13A	GRCh38.p7	12:110027793	CAATGAGCTTTCATT[A/G]CAGTTAGATGAAAGG	88455
rs772546917	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022311	AAAATTAGCCAGACG[C/T]GGTGGCGGGCGCCTG	88455
rs772626602	snp	A/C	3.29484e-05	0.00405871	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028552	CAAACAACCCCACAG[A/C]CATCACGCCTGATGA	88455
rs772626620	snp	C/T	1.65002e-05	0.00287225	intron-variant	ANKRD13A	GRCh38.p7	12:110016469	TATTTATTTCTCTTT[C/T]TAAATTTACTTAGCC	88455
rs772641038	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110030086	GAAGAGTATTAATTT[G/T]GGATAGTTGTATGTT	88455
rs772641974	snp	C/T	3.30617e-05	0.00406568	intron-variant	ANKRD13A	GRCh38.p7	12:110029428	AGCAATAATCTCCTT[C/T]TCCCATCTGGTGGAG	88455
rs772710854	snp	A/G	1.64776e-05	0.00287028	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018454	AAACATGAGCTGGAT[A/G]AGAGGGAGGCGTAGT	88455
rs772729715	snp	C/T	3.50134e-05	0.00418395	intron-variant	ANKRD13A	GRCh38.p7	12:110019092	GCTTCCTTGTTTTTG[C/T]ATCTTCCCTACTTTG	88455
rs772779344	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027139	AAAACATTGCATGTG[A/G]TTGCCACATCCCAGC	88455
rs772801496	snp	A/C	1.64803e-05	0.00287052	missense, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033897	GCATTTGCAAGATGA[A/C]GATTACGAGATAATG	88455
rs772901756	snp	A/C	2.09729e-05	0.00323821	intron-variant	ANKRD13A	GRCh38.p7	12:110012153	GTAAGTATACTTTTA[A/C]AATAATTTAAAGTCC	88455
rs772989142	snp	A/C	1.69117e-05	0.00290785	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037556	TCACTGACAAATAGA[A/C]CTTTCAGCCTGTGAG	88455
rs773132810	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012996	GAAGTCATGATCATC[C/G]TGGTAAGGTTGGACT	88455
rs773139784	snp	C/T	1.6492e-05	0.00287154	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012009	TTCCTTCACAGAATG[C/T]GGAGGCTGTGGACCC	88455
rs773188407	snp	A/C			upstream-variant-2KB, intron-variant	ANKRD13A	GRCh38.p7	12:109999327	AGCTGGAGGTGGGTG[A/C]AATGGCGCGGACCCC	88455
rs773190365	snp	C/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028590	AATGAAGAGTTTGAT[C/G]TGAAAGACAGGGACA	88455
rs773224964	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004413	CTGAGGTCGGGAGTT[C/G]GAGACCAACCTGACC	88455
rs773264065	in-del	-/CATA			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038991	AGGTAACGTCTGTAT[-/CATA]CAGTTAGTGTTGCCA	88455
rs773274467	snp	C/G	1.64789e-05	0.0028704	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013246	GCTCCAAAAAATTCT[C/G]GAGGTATCCATGAAA	88455
rs773457423	snp	G/T	3.30153e-05	0.00406283	splice-donor-variant	ANKRD13A	GRCh38.p7	12:110029637	TCCTGTCAAAATAGG[G/T]ACTGCTAAATAAACT	88455
rs773548364	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008487	GCATTTGTCATCAGG[A/G]TAATAGTGGGTTCAT	88455
rs773564873	snp	C/T	1.6473e-05	0.00286988	intron-variant	ANKRD13A	GRCh38.p7	12:110036245	TATTCATGTCTATCA[C/T]ATTTGTCTTTGCCAG	88455
rs773576268	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030237	AGTGGCATGATCTTG[A/G]CTCACTGCAACCTCT	88455
rs773616285	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110014918	CCTCCCGAGTAGCTG[A/G]GACTACAGGCGCCCA	88455
rs773618931	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030661	AATTCCCTTGTTTCA[C/T]GTCTTAAATGCACGG	88455
rs773639994	snp	C/T	1.65679e-05	0.00287814	intron-variant	ANKRD13A	GRCh38.p7	12:110025839	GTAATCACCACCACC[C/T]TCCCACCTCCTGTTT	88455
rs773757209	snp	C/G	3.29766e-05	0.00406045	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013144	ACATGAGGCTGTGAG[C/G]ACTGGCGATCCTGAG	88455
rs773805828	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032318	AACTATCATGATGGT[C/T]CTATGTTTCTCCCCT	88455
rs773899515	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014574	GAAGCTGTCATTGAT[G/T]TCTTGTCTTTCAACA	88455
rs773905891	in-del	-/T	3.30426e-05	0.0040645	intron-variant	ANKRD13A	GRCh38.p7	12:110018314	TTCTTGGCCCTTGAG[-/T]TTTTCTCAGTAGTAC	88455
rs773917972	snp	A/G			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039734	AAGCTCTGCATCAAT[A/G]CTATCCCTTGAAGCC	88455
rs773934551	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110016635	TCATCCGGTCTTCCC[C/T]GCCATGCATAGGACT	88455
rs774007456	snp	C/T	1.6743e-05	0.0028933	intron-variant	ANKRD13A	GRCh38.p7	12:110013091	GAATTTGTCAGAAAG[C/T]ATGAGAATTAAATTT	88455
rs774020765	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002027	TCAAGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	88455
rs774041946	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038652	AATCTATTTTTTAAC[A/G]ATCTTTTTATTATTT	88455
rs774042457	snp	C/T	1.64977e-05	0.00287203	intron-variant	ANKRD13A	GRCh38.p7	12:110029458	GATGACCTCAGTCTT[C/T]TCTTGGTTGAATTCT	88455
rs774080017	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003286	AGTATAGCACCTAGG[A/T]AAGAGGAGGACATTC	88455
rs774112727	snp	C/T	4.94189e-05	0.00497062	missense	ANKRD13A	GRCh38.p7	12:110036264	TGTCTTTGCCAGGAA[C/T]TTTCAGGACCAGCTT	88455
rs774130935	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004081	GAGAATCGCTTGAAC[C/G]TGGGAGGCGGAGGTT	88455
rs774212742	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026993	AGGGCTTGTTTATGT[C/G]TTATCAAGAACAATT	88455
rs774214820	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010987	GCTCATGCCTTTAAT[C/T]CCAGCTACTAGGGAG	88455
rs774236686	snp	A/G	1.74503e-05	0.00295379	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030682	AAATGCACGGATTAC[A/G]TTTGGAAATGTTAAT	88455
rs774316993	snp	C/T	1.7457e-05	0.00295435	intron-variant	ANKRD13A	GRCh38.p7	12:110019103	TTTGCATCTTCCCTA[C/T]TTTGCACTTAGTTAT	88455
rs774324350	snp	A/G	6.65137e-05	0.00576649	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019303	ATTAACACCAGCCTC[A/G]ATACTAAAAATATTG	88455
rs774337243	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110011954	TCAAGCACATTTCCC[A/T]ATTTTAATGTAATAC	88455
rs774380645	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033449	AAGTGTTCAGATATT[C/T]TATATATACTTTTAT	88455
rs774392967	snp	A/G	0.000131776	0.00811608	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029586	TCATTTTGCAAGACT[A/G]AGAGATTTCATCAAA	88455
rs774516968	snp	G/T	1.70778e-05	0.00292209	intron-variant	ANKRD13A	GRCh38.p7	12:110030790	ATACAAAGTTTAGTT[G/T]TGTTATTTAAAAAAA	88455
rs774562473	in-del	-/AAGA			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997571	GAGATGAAAATGAAG[-/AAGA]GAGAGAGGGAAATAA	88455
rs774652767	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008154	GATGCTTTTTGAGGA[A/T]GTTTCCTTTTATTCC	88455
rs774659324	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035866	GCTGCAGTGAGCTAC[A/G]ATCACATCACTACCC	88455
rs774677108	snp	A/G			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039600	AGGTTAACAAGCCCC[A/G]TGCTGCTTGTTTCAA	88455
rs774680548	snp	G/T	1.75016e-05	0.00295813	intron-variant	ANKRD13A	GRCh38.p7	12:110023958	TCACTAACTTAAGCT[G/T]GGGGGGAAAAAAACT	88455
rs774747248	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022241	GATCACGAGGTCGGG[A/T]GATCGAGACCATCCT	88455
rs774756849	snp	C/T	1.64863e-05	0.00287104	intron-variant	ANKRD13A	GRCh38.p7	12:110016451	GAGTGGCTGTGGGCT[C/T]GTTATTTATTTCTCT	88455
rs774785959	snp	A/G	1.66707e-05	0.00288705	intron-variant	ANKRD13A	GRCh38.p7	12:110025856	CCCACCTCCTGTTTT[A/G]TTGTTATTTTTTAAG	88455
rs774875943	snp	A/G	1.65403e-05	0.00287574	intron-variant	ANKRD13A	GRCh38.p7	12:110027790	AAGCAATGAGCTTTC[A/G]TTGCAGTTAGATGAA	88455
rs774895845	snp	A/G	1.65143e-05	0.00287348	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037414	TGCCCCAGCGCCCTG[A/G]GCGAGACAAGCCGTT	88455
rs774911262	in-del	-/TGTT			intron-variant	ANKRD13A	GRCh38.p7	12:110019773	ATATAGTTAAATGTT[-/TGTT]TGTTTGTTTGTTTGT	88455
rs775009530	snp	C/T	1.6859e-05	0.00290331	intron-variant	ANKRD13A	GRCh38.p7	12:110037320	CCACCATGATGATGA[C/T]AGTAGTGACTCTCCC	88455
rs775091528	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029916	CATGACACAGTCATT[G/T]TTTTAATGTCAAACC	88455
rs775174372	snp	C/T	6.74787e-05	0.00580816	intron-variant	ANKRD13A	GRCh38.p7	12:110025872	TTGTTATTTTTTAAG[C/T]CTAGAGGGAACTCTT	88455
rs775295917	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038350	GCTAATCCTGTCCCT[A/G]AAGGAGCAGCTAGGG	88455
rs775342267	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110001766	TAAACTTTTGTGAGA[C/G]TCATCGTTCTTAATT	88455
rs775362594	snp	A/G	1.64811e-05	0.00287059	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029617	TTGGAATTCCCACCT[A/G]GATTTCCTGTCAAAA	88455
rs775395329	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003038	AAGTTGGTTGCTGAA[C/G]TTGAAACTGTTTGTG	88455
rs775411501	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010861	GCGTATCTTCAGAGA[C/T]TGCAGGGGTAGTTAG	88455
rs775458531	snp	G/T	1.64808e-05	0.00287057	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012030	CTGTGGACCCACGAG[G/T]TCGAACATTATTGCA	88455
rs775484007	snp	A/G	6.59304e-05	0.00574116	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033847	GTGTTTGAAATTCCC[A/G]AATCTTACTATGTTC	88455
rs775539484	snp	A/G	0.000131961	0.00812176	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019271	GGGAAGTTGAGCGGC[A/G]GCTCACAAGCCCTGT	88455
rs775568103	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009986	TCTCCTGCCTCAGCT[A/T]CCCGAGTAGCTGGGA	88455
rs775666144	snp	C/T	1.64993e-05	0.00287218	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024075	TCTGGGGCTGGAGGA[C/T]AGATAAAGCAGAAGT	88455
rs775817676	snp	A/G	1.89507e-05	0.00307815	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012136	TCGCCAGGGATGGAC[A/G]GGTAAGTATACTTTT	88455
rs775821904	snp	A/T			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034045	TAATCTGAAAGATTT[A/T]TTCTAAATATCAAGT	88455
rs775848255	snp	C/G	5.39418e-05	0.00519307	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037596	AAAGCAGAGGCTGTG[C/G]GCTGTCACAGATGCT	88455
rs775912952	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110005342	TAGAGAAAATGTGTC[A/C]CTATGTTGCCCAGAC	88455
rs776028800	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028572	ACGCCTGATGAGTAC[C/T]TCAATGAAGAGTTTG	88455
rs776039583	in-del	-/TTC			intron-variant	ANKRD13A	GRCh38.p7	12:110015652	CCCAGGTTCAAGCAA[-/TTC]TTCTGCCTCAGCCTC	88455
rs776140711	snp	A/C	1.65767e-05	0.00287891	intron-variant	ANKRD13A	GRCh38.p7	12:110027815	GATGAAAGGAAACAA[A/C]TTGTCTGTGTCTGGG	88455
rs776166153	in-del	-/GA			intron-variant	ANKRD13A	GRCh38.p7	12:110001762	ACGATAAACTTTTGT[-/GA]GAGTCATCGTTCTTA	88455
rs776188398	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018425	CGCGTCGATATCACA[C/T]TGCTGGGATTTGAAA	88455
rs776223267	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025962	TTCTTCTCTCTCTCT[C/T]TCTTTTTTTTTTTTT	88455
rs776228536	snp	C/T	1.65012e-05	0.00287234	intron-variant	ANKRD13A	GRCh38.p7	12:110018329	TTTTTCTCAGTAGTA[C/T]ACTTCTCTCCTCCAG	88455
rs776285783	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110012307	GGAGGTTGACACTGC[A/C]GTGAACTGTGATTGC	88455
rs776309776	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027241	GAAATGCAGGTGATA[C/G]CCAACCTTCCTTAGA	88455
rs776336442	in-del	-/TTTG			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039065	CATTTCACAATCTGT[-/TTTG]TTTTTTTTTTTTGTC	88455
rs776338439	in-del	-/TGA			intron-variant	ANKRD13A	GRCh38.p7	12:110005004	TAAACATATACAGAT[-/TGA]TTTTTTCAAAAGATT	88455
rs776366103	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028795	TAGGCTGGAGTGCAG[C/T]GGCACGAACTCGGCT	88455
rs776556231	in-del	-/A	3.41111e-05	0.00412969	intron-variant	ANKRD13A	GRCh38.p7	12:110033767	AAATGTAATGAACTC[-/A]AGACACTGGACGGTT	88455
rs776564226	snp	G/T	1.65138e-05	0.00287343	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019284	GCGGCTCACAAGCCC[G/T]GTCATTAACACCAGC	88455
rs776569548	in-del	-/GAGG			intron-variant	ANKRD13A	GRCh38.p7	12:110018035	GTTGCATATGTGAGT[-/GAGG]AAGGCCAGATGTACA	88455
rs776590546	snp	C/T	0.000137448	0.00828884	intron-variant	ANKRD13A	GRCh38.p7	12:110021101	TTTTGTATTTTTGTG[C/T]CCACAGGGTTTTCAG	88455
rs776598093	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022806	CCCCTGTGACTGTTA[C/T]CTTGTTTCTGAAGTG	88455
rs776615008	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037039	ATTACGGGAAAAACC[A/G]CGAGGATTCATTTTA	88455
rs776687587	snp	C/T	1.65798e-05	0.00287917	intron-variant	ANKRD13A	GRCh38.p7	12:110025715	TGATTCCCTGTGTCA[C/T]TGTTTTCTTTCGCAT	88455
rs776707541	snp	G/T	1.65754e-05	0.00287879	intron-variant	ANKRD13A	GRCh38.p7	12:110013115	TAAATTTCACCCTTT[G/T]GTTTTCTAGTTTTAC	88455
rs776887986	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030527	GAAGGGTTGTTATGA[A/G]GCTTAAATAAAATTA	88455
rs776930246	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009936	ATGGCACAATCTCAG[C/T]TCACTGCAACCTCCG	88455
rs776973378	snp	C/T	3.29598e-05	0.00405941	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029481	TGAATTCTGCAGGTT[C/T]AAAGCAATGTTGTGG	88455
rs777010777	snp	C/T			intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032498	CAGCTAAGGAACACT[C/T]GTGCACTCTTGGCTG	88455
rs777062139	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033654	TTTTTCTGTCATGCT[G/T]CCTCAGAATCTCTCA	88455
rs777068402	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003700	GGGCAAGCTGGAAGG[A/G]GTGTCCAGTTGTCTG	88455
rs777085804	snp	C/T	1.6477e-05	0.00287024	missense, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033881	ACAATGGCAGAAATG[C/T]GCATTTGCAAGATGA	88455
rs777174427	snp	C/T	3.31807e-05	0.00407299	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024103	AGTTGTTAATGGTTA[C/T]GAAGCAAAGGTAAAA	88455
rs777243670	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036397	CAGGCGAGCAGACGC[A/G]TGGCACTGTGCATTT	88455
rs777402784	in-del	-/TG			intron-variant	ANKRD13A	GRCh38.p7	12:110034444	GTAAGCAGTAGGCTT[-/TG]TGTGTGTGTGTGTGA	88455
rs777424454	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021554	CTTTAGCCTCCCGAG[G/T]AGCTGGGATTATAGG	88455
rs777424498	snp	C/T	3.3065e-05	0.00406588	intron-variant	ANKRD13A	GRCh38.p7	12:110024023	TGTACATGTAGAAAT[C/T]TGTGGTGTTCACTTT	88455
rs777439493	snp	A/G	1.65274e-05	0.00287462	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019174	GAAGTCAACCATGAT[A/G]ACAAAGTGGTCACCA	88455
rs777439576	snp	A/G	8.07168e-05	0.00635231	intron-variant	ANKRD13A	GRCh38.p7	12:110030605	ATTATTGTTATTCTC[A/G]GTAAAGTTTACTTAT	88455
rs777497643	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007564	TTTGTATTTTTAGTA[C/G]AGGTGGGGTTTCTCC	88455
rs777618329	snp	A/G	8.99871e-05	0.00670712	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033990	CTCTAATGGCAGGGC[A/G]TGGGAGGTCTTACCC	88455
rs777634727	snp	A/G	1.72549e-05	0.0029372	intron-variant	ANKRD13A	GRCh38.p7	12:110024154	TTAATATAGCTATTT[A/G]GCTTCTATGCAAATG	88455
rs777644910	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028716	TATGGTGTTATGTTG[G/T]ATCATTCCACTGCCC	88455
rs777815887	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018374	AGAATATGCCCAAAT[A/G]ATGTCTGTCGCATCT	88455
rs777880155	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015615	GGAATAGTGCTATCT[C/T]GGCTCATGGCAACCT	88455
rs777903529	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034947	AACAGTGCTCACACT[C/G]CAGCGTCCTCACTGG	88455
rs777926579	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002659	TATCACCCCAGCAAT[A/G]AAGTGGCTGTTTCCC	88455
rs778027549	snp	C/T	1.64746e-05	0.00287002	intron-variant	ANKRD13A	GRCh38.p7	12:110036333	CAGTATGAGAGGTGA[C/T]TGACTGACGTGACTC	88455
rs778204392	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022366	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	88455
rs778307850	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110033530	GTGCGTATATGTTTA[A/G]GGGGAGAAATCTGCG	88455
rs778358926	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017863	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	88455
rs778371129	in-del	-/T	1.65018e-05	0.00287239	intron-variant	ANKRD13A	GRCh38.p7	12:110029455	GAGATGACCTCAGTC[-/T]TTTTCTTGGTTGAAT	88455
rs778380328	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010490	ACTAAGGTAAGAGAA[C/T]CTAGAAGATATTAAT	88455
rs778468318	snp	A/G	3.3036e-05	0.0040641	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037400	GCACAGAAGGCCTGT[A/G]CCCCAGCGCCCTGAG	88455
rs778502476	snp	A/G	1.73003e-05	0.00294106	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030716	TGTAGCACTGCCGAA[A/G]AATCTGTATCTCAAA	88455
rs778667606	snp	A/T	4.94866e-05	0.00497402	intron-variant	ANKRD13A	GRCh38.p7	12:110016366	AAGGGTAATCTGTTT[A/T]AAACCTTTGTCTGCC	88455
rs778669144	snp	A/G	3.2962e-05	0.00405954	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025799	ACAGAACATCTGACC[A/G]AGGAGGAAAAAAAGA	88455
rs778682050	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019069	GATGATACATTTTAA[C/T]ATACGAAGCTTCCTT	88455
rs778713322	in-del	-/A					GRCh38.p7	12:110035611	CGCACCACCAGACCC[-/A]GCTAGTTTTTGTGTT	88455
rs778764380	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110004523	GGGAGGCTGAGGCAG[G/T]AGAATTGCTTGAACC	88455
rs778941002	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029129	GCTCCTTTCCAAATA[C/G]AATCTAGATTGGATG	88455
rs779013105	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001065	CCTGGCTGAGAAACT[C/T]TGCTTTTAAAGTCTC	88455
rs779041870	snp	C/T	6.58957e-05	0.00573964	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018407	AAAAGTGGTGCCAAA[C/T]TGCGCGTCGATATCA	88455
rs779049689	snp	C/T	1.64863e-05	0.00287104	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033844	TCTGTGTTTGAAATT[C/T]CCGAATCTTACTATG	88455
rs779063482	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013632	AAAAATTAGCAGGGC[A/G]TGGTAGTGCATACCT	88455
rs779126124	snp	A/G	6.59152e-05	0.00574049	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028628	GCCGAAAGAGCTGAC[A/G]ATTAGAACACAGAAG	88455
rs779153669	snp	G/T			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998968	CTTTTATGCAAATAC[G/T]GTATTTGAAGCCACT	88455
rs779314629	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036566	CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	88455
rs779353067	snp	C/G	1.6516e-05	0.00287362	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037407	AGGCCTGTGCCCCAG[C/G]GCCCTGAGCGAGACA	88455
rs779433142	snp	A/C	1.656e-05	0.00287745	intron-variant	ANKRD13A	GRCh38.p7	12:110011970	ATTTTAATGTAATAC[A/C]TCCAATTATGTAAAT	88455
rs779444239	snp	C/T	4.96142e-05	0.00498043	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037492	GAGGAATGGGAGCTC[C/T]GGCTCCAGGAGGAAG	88455
rs779508531	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032132	GCTGTCCTTGTCTTG[G/T]TCCTGGTTCTAGGGG	88455
rs779530411	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009333	TGATCCACCCGCCTC[A/G]GCCTCTCAAAGTGTT	88455
rs779607468	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028539	GAATGTGCTACTGCA[A/G]ACAACCCCACAGCCA	88455
rs779608082	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014080	ATTTATAGAGAAAAA[-/T]TTAATAGCTCTATCG	88455
rs779622295	snp	A/C	0.000102923	0.00717293	intron-variant	ANKRD13A	GRCh38.p7	12:110023972	TGGGGGGGAAAAAAA[A/C]TATAAAGGCTACAGA	88455
rs779700058	snp	A/G	6.64121e-05	0.00576209	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033811	GCTTCCCACATCACA[A/G]ACTTTGAGGTTGATC	88455
rs779708726	snp	C/T	3.31917e-05	0.00407367	stop-gained, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012092	GCTCGAGTCTTACTC[C/T]GACATAAAGCAGATG	88455
rs779811874	snp	A/C	1.64803e-05	0.00287052	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016389	TGTCTGCCCTTCAGG[A/C]TCCGGATTTCTATGT	88455
rs779916353	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110012770	TTTGTGTTGACTGAG[-/C]CAGGGATACTGTAGG	88455
rs780099189	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004268	GGGTATTTTTATTTG[A/G]GTATAGCTCATGGCT	88455
rs780130640	snp	C/G	1.87061e-05	0.00305822	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034004	CGTGGGAGGTCTTAC[C/G]CTCTGGGTTAGCCTC	88455
rs780152225	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110005903	CTCTCTGCAACCTCT[A/G]CCTCCTGGGTTTAAG	88455
rs780181224	snp	C/T	2.07803e-05	0.00322331	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030754	AGGGACCCAGGCTGA[C/T]TCAGGTAAAAAAATA	88455
rs780181458	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028067	CAGGACTTTATATTG[C/T]AACAGAGCACCTTAA	88455
rs780184483	snp	C/T	1.65847e-05	0.0028796	intron-variant	ANKRD13A	GRCh38.p7	12:110025710	AGTTTTGATTCCCTG[C/T]GTCACTGTTTTCTTT	88455
rs780197864	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012869	ACTGTCTAAACACAT[A/T]ATCAGGATTTCGCAA	88455
rs780250903	snp	C/T			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998878	AGCATCCTACAAGGA[C/T]CGGACAACCCCCACA	88455
rs780258923	snp	A/G	3.36768e-05	0.00410333	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019142	TTCCATTAATAGACA[A/G]CTGGGCGGAGTTAAT	88455
rs780270497	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006721	CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGATTA	88455
rs780284031	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011752	GTTGGATGATCTGGA[A/G]CCTGTTGCCAACATT	88455
rs780295952	snp	A/G	1.64852e-05	0.00287094	intron-variant	ANKRD13A	GRCh38.p7	12:110028650	ACACAGAAGTAAGAG[A/G]GGTTCAGCTGCCATT	88455
rs780306030	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035334	TACTGGCTGGGTGCA[C/G]TGGCTCATGCCTATA	88455
rs780466148	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028554	AACAACCCCACAGCC[A/G]TCACGCCTGATGAGT	88455
rs780543192	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013539	CCACTTTGGGAGGCT[-/G]AGGCAGGAGGATTTG	88455
rs780547986	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036500	CACGCCTATAATCCC[A/G]GCATTTTGGGAGGCC	88455
rs780555673	snp	A/C	0.000101087	0.00710867	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012111	ATAAAGCAGATGTGA[A/C]AAAAGAAAATCGCCA	88455
rs780638068	in-del	-/TAT	6.61868e-05	0.00575231	intron-variant	ANKRD13A	GRCh38.p7	12:110025728	ACTGTTTTCTTTCGC[-/TAT]ATACACCTCTCAGGT	88455
rs780668787	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110020885	TGAGTGAATCTGGAG[A/G]TGAAATCTCCAAAGT	88455
rs780732904	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024273	TTTGATTTTGTCTTA[C/T]TTGACTTTCAGAAAA	88455
rs780832981	snp	A/G	3.42027e-05	0.00413523	intron-variant	ANKRD13A	GRCh38.p7	12:110024144	AAAATAAGATTTAAT[A/G]TAGCTATTTAGCTTC	88455
rs780851488	snp	A/G	3.30262e-05	0.0040635	intron-variant	ANKRD13A	GRCh38.p7	12:110012180	GTCCGTCTGAGCACC[A/G]TGGTGAAACCCTGTC	88455
rs780940221	snp	C/T	1.65162e-05	0.00287365	intron-variant	ANKRD13A	GRCh38.p7	12:110028675	GCCATTTTCAACCTA[C/T]GTATGTTTCAGAAAT	88455
rs781065986	snp	A/C	2.44705e-05	0.00349781	intron-variant	ANKRD13A	GRCh38.p7	12:110030763	GGCTGATTCAGGTAA[A/C]AAAATAAATAAATAC	88455
rs781116951	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110031752	ATCAATACAATTCAT[G/T]ATTTTAGATGCAATT	88455
rs781150657	snp	C/G	1.65211e-05	0.00287407	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037385	AGAGCCTCCTCACCA[C/G]CACAGAAGGCCTGTG	88455
rs781264394	snp	G/T	6.60666e-05	0.00574708	intron-variant	ANKRD13A	GRCh38.p7	12:110025828	GAGATATAAAGGTAA[G/T]CACCACCACCCTCCC	88455
rs781286699	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110003841	CAGCCTGGCCAATAT[A/T]GTAAGACTCCGTCTC	88455
rs781293187	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017570	AAAAGAATAGAACTT[C/T]AGATTGTTTTGAGAA	88455
rs781298998	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010169	CCGCGCCTGGCTGAG[-/T]TTTGAGTGTTAATCC	88455
rs781317410	snp	A/G/T	3.31462e-05	0.0040709	intron-variant	ANKRD13A	GRCh38.p7	12:110024015	TGGCATATTGTACAT[A/G/T]TAGAAATTTGTGGTG	88455
rs781330413	snp	A/G	3.29473e-05	0.00405864	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110036319	ACACCTATGACGCCC[A/G]GTATGAGAGGTGATT	88455
rs781331324	snp	A/G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026454	TGGTGGCCCATGGCT[A/G/T]TAATCCCAGCTACTC	88455
rs781353037	snp	A/G	1.64762e-05	0.00287016	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013185	CAGTTCTCCAACATC[A/G]AGACTACCACAACAC	88455
rs781356844	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039191	TTTGCATTTACCGTG[A/G]GCAAAGATACTTCTT	88455
rs781412100	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110024150	AGATTTAATATAGCT[A/G]TTTAGCTTCTATGCA	88455
rs781429761	snp	A/G			missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019158	CTGGGCGGAGTTAAT[A/G]GAAGTCAACCATGAT	88455
rs781431177	snp	G/T	1.6519e-05	0.00287388	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027764	CAATTTGGTGCACAA[G/T]GGGTAAGTTGAAGCA	88455
rs781511186	in-del	-/CTT			cds-indel	ANKRD13A	GRCh38.p7	12:110038039	ATCTGTGCTGATCTC[-/CTT]ATTTTTACCTTTTTA	88455
rs781592478	in-del	-/A	1.66181e-05	0.00288249	frameshift-variant, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037529	GCTCCAGCAAGTCTT[-/A]ACAGCTGTCACTCAC	88455
rs781616233	snp	C/T	3.31296e-05	0.00406985	intron-variant	ANKRD13A	GRCh38.p7	12:110018520	GTAGTAATCACTGCT[C/T]AAGCAAAATTACAGG	88455
rs781655121	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110021988	GGCCTTTGGTGTGGT[C/G]TCAGTGGAGACAGGC	88455
rs781668695	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110011571	CTGACCCAAATTATC[C/T]GTGCTTTCAGTTTTG	88455
rs781694896	snp	C/G/T	0.00024718	0.0111146	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019238	GCCTCACTCTGGACT[C/G/T]GATGAAGCCAAAAAG	88455
rs796095508	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007623	GACCTCAGGTGATCC[A/G]CCCACCTCAGCCTCC	88455
rs796267870	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110011122	AGAAAAAAAAAAAAA[-/A]GGTTGTACTTTCCAA	88455
rs796343052	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002052	CCCAAAGTGCTGGGA[A/T]TACAGGCATGAGCCA	88455
rs796391638	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110031880	TTTATCTTTTTTTTT[-/T]CTTACACAATTGCAT	88455
rs796522876	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022075	TGCATGCAAAGTTAC[C/T]AAGGGCCACAGAGTT	88455
rs796913578	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033220	ACCACGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT	88455
rs796993293	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015898	TTATATCAAGGTAAA[A/G]TAACACTCTAATATT	88455

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