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

RFWD3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs368570567	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621376	CTAGAAGTGAAAGAG[A/C]CAAAAGGCACTAGGA	55159
rs368599533	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667129	ATGGGAGGTTTTTTT[G/T]TTTTTTTTTTGTTTG	55159
rs368615205	snp	A/C/G	0.000148976	0.00862957	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630942	ATAAGTCTGGACCAC[A/C/G]GTATTTGTCTCCAGG	55159
rs368623168	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74658925	GGTGTGTGCCACCAC[A/G]CCCGGCTAATTTTTT	55159
rs368624933	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621603	AGGAATATGGTGGGG[C/T]AGAGACTGGTGGAGC	55159
rs368627580	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74630358	CCGCCTCGTCTTCCC[A/C]AAGTGCTGGGATTAC	55159
rs368629693	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74649273	CAGGTATGAGAAGCT[A/G]GCAGGAGAGAGCCTG	55159
rs368634908	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74636437	GCAGTTTCCTGCCTG[A/G]GATACTGTGAAGGTC	55159
rs368688486	snp	A/T	2.0087e-05	0.00316908	intron-variant	RFWD3	GRCh38.p7	16:74624107	GAAGGGTCAGGAGTC[A/T]GTCAGTACACGAAGG	55159
rs368841030	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623759	CATAACAGATACACA[A/G]TCTGTAGTGTCTCAG	55159
rs368851610	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662326	TTGTGAAGTAAGGCA[C/T]GTGCTTTTATTTTCA	55159
rs368895192	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650222	TAGAAAGATGTTCCA[C/T]TTGTAGACTGTTCTA	55159
rs368956444	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646388	CTCAAAAAAGTTCAG[C/T]GTAGCATGATTTATA	55159
rs369018874	snp	C/T	0.000187191	0.00967267	intron-variant	RFWD3	GRCh38.p7	16:74630985	AAAAGACTTTTACAA[C/T]TGCATTAAGAAAATC	55159
rs369034533	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74643627	GTGTGTATGTTCTTT[-/T]AATATTTTTGAAGCA	55159
rs369038170	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647883	AGGCATGGGCCACCG[C/T]GCCCAGCCCATTATT	55159
rs369048069	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659139	TTGTAAGTTGGCATC[C/T]GGTTTATAAGTGTCA	55159
rs369100110	snp	A/C/G	0.00013257	0.00814056	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623918	TGCCTTCAAGGTTTC[A/C/G]AGACCACAGTCACTC	55159
rs369109128	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662126	TTGAAAACTACCACC[C/T]AGTTTTTAAACTAAA	55159
rs369195135	snp	C/G	3.35475e-05	0.00409544	missense, intron-variant	RFWD3	GRCh38.p7	16:74630791	CCTACCTGGCTTTCT[C/G]AGCTACTAACTCCTG	55159
rs369203376	snp	A/G	9.88403e-05	0.00702925	intron-variant	RFWD3	GRCh38.p7	16:74644498	TGGTTCTAGGAATCT[A/G]CCTGACTTAACATGT	55159
rs369236335	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74634690	CACTGTGCCCACTTG[A/G]GTTAAATTCTTTAAA	55159
rs369345096	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663179	AAAGTGCTCGGATTA[C/T]AGGCATGAGCCACCG	55159
rs369457640	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637661	ATAAAATTCAGACTA[C/T]AGTAGACCTCATCAT	55159
rs369484750	snp	C/G	8.79918e-05	0.00663236	intron-variant	RFWD3	GRCh38.p7	16:74660909	ACAGCAATGATCACA[C/G]ACTTATCCATATATT	55159
rs369486590	snp	C/T	3.31603e-05	0.00407174	intron-variant	RFWD3	GRCh38.p7	16:74632482	CCATGCTACTCAACA[C/T]CAAAGAGCCCAGTCT	55159
rs369671650	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629527	AGTCAGGTGTGGTGG[C/T]ACACGCGTATAGTCC	55159
rs369694217	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74628223	GGCTAATTCACTTCC[A/G]GGAGTACCTGGCAGA	55159
rs369698726	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74637837	CAAAAGTTCTTTGGA[C/T]TAGAAAGGACAAACG	55159
rs369798440	in-del	-/CTTT			intron-variant	RFWD3	GRCh38.p7	16:74655628	GTCTGTGCTCTCTCT[-/CTTT]TTTTTTGAGATGGAG	55159
rs369856889	snp	C/G	1.64749e-05	0.00287005	missense	RFWD3	GRCh38.p7	16:74651994	GAGCTGTCACTGTCA[C/G]AATCAGAACTACTAG	55159
rs369886677	snp	A/C/G	9.89551e-05	0.0070334	synonymous-codon	RFWD3	GRCh38.p7	16:74632525	CCAAATCACTCACCT[A/C/G]GTCAGTTTAATAGTG	55159
rs369898970	in-del	-/CT	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74651443	GGCAACATGGAAAAA[-/CT]CTGTCTCTACAAAAA	55159
rs369912157	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658834	TTACAGTGACAAGAT[A/C]TTGGCTCACTGCAAG	55159
rs369913815	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653136	TTGTGCCTAGGAGTT[C/T]GAGACCAGCCTGATT	55159
rs369920737	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622565	TCTAGTGCAACAACC[C/G]CTTGCCGGAGAGAAA	55159
rs369932039	snp	C/G/T	7.52405e-05	0.00613315	intron-variant	RFWD3	GRCh38.p7	16:74637992	GGGGAAAGCCAGCAA[C/G/T]AAGTGGGGATTAGGA	55159
rs369954619	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74645987	TCTCCTGACCTCGCG[A/C]TCCGTCCGCCTTGGC	55159
rs370165644	snp	A/G	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74652111	AAGTAAGCATCCAAT[A/G]GTGCTCTCAACCTAT	55159
rs370165832	snp	C/T			synonymous-codon	RFWD3	GRCh38.p7	16:74661159	ATGTTGTTCTGAAGT[C/T]CTTGGATTGATGTTC	55159
rs370213248	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74657574	TCCACCTCCCGGGTT[C/G]AAGCGATTCTCCTGC	55159
rs370216573	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74626820	AAGAGAAAAACAATT[C/G]TGTGAGTTGTCTGTT	55159
rs370237434	snp	A/C/T	0.00101283	0.0224824	intron-variant	RFWD3	GRCh38.p7	16:74649094	CTAAAAATAAATAAA[A/C/T]AAATAAATAGATTTT	55159
rs370346769	snp	A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74643837	TCCGCCACTATGCCC[A/G]GCTAATTTTTTTGTA	55159
rs370456974	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647793	GATGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT	55159
rs370479162	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74626722	ATATCACAGCATCAA[C/T]GAAATTTAGAACCGT	55159
rs370481587	in-del	-/CA			intron-variant	RFWD3	GRCh38.p7	16:74627079	AGTCACAACAAATCA[-/CA]GTCTTGGAGACAGCC	55159
rs370553790	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74635824	GCATTTGAAAAGACT[A/T]GGTTTTCAACATTTA	55159
rs370644134	snp	C/T	0.000174554	0.00934057	intron-variant	RFWD3	GRCh38.p7	16:74652156	AACGGAATTATAGTA[C/T]AATGAACTATCATCA	55159
rs370695654	snp	A/G	3.30857e-05	0.00406716	synonymous-codon	RFWD3	GRCh38.p7	16:74661327	GCTGCTGACCACATC[A/G]GCAGGAACAGGCTGG	55159
rs370831188	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663889	GGCAATATTGAAAGA[C/T]GGCGCTAAAAGAGAA	55159
rs370931038	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653879	CTACTCAGTGTCCAA[C/T]TCAATAGACAGAAGA	55159
rs370953400	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74639263	GGCTGGTCTCAAACT[A/C]CTGGCCTCAAGTGAT	55159
rs370956327	snp	G/T	1.6546e-05	0.00287624	intron-variant	RFWD3	GRCh38.p7	16:74649122	TTTTTTAAAATGATG[G/T]TCATATTACCTGTTT	55159
rs370961000	snp	C/G	6.58892e-05	0.00573936	missense	RFWD3	GRCh38.p7	16:74636432	ATCCGGCAGTTTCCT[C/G]CCTGAGATACTGTGA	55159
rs371120350	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632491	TCAACACCAAAGAGC[C/T]CAGTCTCCACCTACT	55159
rs371136829	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74660339	GCGCCTGTAATGCCA[C/G]GTACTGGGGAAGCTG	55159
rs371157362	snp	A/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668488	TTGAGGATGGAGGAG[A/T]CGTTTTCATCTACAT	55159
rs371174466	snp	C/T	3.34292e-05	0.00408821	intron-variant	RFWD3	GRCh38.p7	16:74628702	CTGTATCTCACACTC[C/T]AAAACTCGGACGGCT	55159
rs371193592	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74625199	AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAG	55159
rs371243988	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74640184	GTCTTGCTCTGTTGC[C/T]CAGGTTGGAGTGCAG	55159
rs371326072	snp	A/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622472	TTCTACAAAAAAATT[A/T]AAAAAAGGAAAAAAT	55159
rs371338423	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641473	TGGCCTAAACAGATT[A/G]ATTTTGACTAGAGAA	55159
rs371348648	in-del	-/CTATA			intron-variant	RFWD3	GRCh38.p7	16:74639944	CACTCACATAACTTA[-/CTATA]GTATACTGGTATAAT	55159
rs371364192	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657900	ATAAGAAGATTTAAT[A/C]AAATACATACTAGAG	55159
rs371369585	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74654665	CTTAGTGAGGAAGGC[A/G]TGTCAAAAGCTGGGA	55159
rs371396855	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629258	CCAAAGTTGCCAAAG[C/T]GTCTACTTTGCCTGT	55159
rs371399366	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647737	GCTGGGATTATATGC[A/G]CCTGCCAACATACCC	55159
rs371419710	snp	A/C/T	3.30755e-05	0.00406655	missense	RFWD3	GRCh38.p7	16:74644686	GTGTCCCCTTCTTCC[A/C/T]CATCCATAGAAGCAG	55159
rs371423726	snp	A/G	0.000153988	0.00877328	intron-variant	RFWD3	GRCh38.p7	16:74636583	TTTGCAAGTCCTAAA[A/G]TGAAAAAGATTTTAT	55159
rs371437388	snp	C/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667944	AACCGCTAAACAGGG[C/G]AGTAAAGACTCCAGT	55159
rs371477101	snp	A/G	8.32674e-05	0.00645188	intron-variant	RFWD3	GRCh38.p7	16:74651871	CCTTCCGAAATTTAA[A/G]CTTCATGGATGTTAG	55159
rs371640440	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659026	TGGCCGCTCAAAGTT[C/T]TGAGATTACAGGCGT	55159
rs371759143	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658376	CTCAGCTAAGCCTGT[C/T]GGGAAGAATAAGCTC	55159
rs371867484	snp	A/G/T	8.52368e-05	0.00652779	intron-variant	RFWD3	GRCh38.p7	16:74630987	AAGACTTTTACAACT[A/G/T]CATTAAGAAAATCAA	55159
rs371871237	snp	C/T	1.66996e-05	0.00288956	missense	RFWD3	GRCh38.p7	16:74661398	GAGCTGGCTGTTGTT[C/T]GGCATGATTTAACTG	55159
rs371926567	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621399	CACTAGGAGCCATTA[C/T]ACATAGCAAATTCTT	55159
rs371942194	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74651339	ATAAAGAATCTAGGC[C/T]GGGTGCAGTGGCTCA	55159
rs372058733	snp	A/G	5.57377e-05	0.0052788	intron-variant	RFWD3	GRCh38.p7	16:74637852	TTAGAAAGGACAAAC[A/G]TACCTGAACACGCCT	55159
rs372082890	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74651757	GATCAAATCCTCTCT[A/G]CATAATTATGGCCAG	55159
rs372178471	snp	A/T	4.52858e-05	0.00475824	intron-variant	RFWD3	GRCh38.p7	16:74637824	TCCATTCCTATTCCA[A/T]AAGTTCTTTGGATTA	55159
rs372197948	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652393	TGGCATCTGGCCATA[C/T]TGTCAGTATCTTTAA	55159
rs372258078	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74626187	CATGGAAACCAAGCA[A/G]TCTCACATACACACA	55159
rs372266012	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639612	TCTCAAGTTACCCTA[C/T]AATAATTTTTAATGC	55159
rs372273896	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654273	ACCAACTTTTTGATT[C/T]GTTCATTTTCTCTCA	55159
rs372335611	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629813	AAATTATCTGTTAAG[A/G]TACTTCAGATTTTGG	55159
rs372342753	snp	A/G	3.36939e-05	0.00410436	intron-variant	RFWD3	GRCh38.p7	16:74630971	GGCTGTGGAGTTACA[A/G]AAGACTTTTACAACT	55159
rs372366918	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630156	ACTGGAGTGCAACGG[C/T]GCAATCTCGGCTCAC	55159
rs372462979	snp	A/G/T	3.66611e-05	0.00428129	intron-variant	RFWD3	GRCh38.p7	16:74661476	CAGTATTTGTAAAAA[A/G/T]TATTAATAAAATAGA	55159
rs372492932	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74648006	CCATGGAGTGCAGTG[C/G]TGCAATCATGGCTCA	55159
rs372511584	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662374	TGGGGGTTCAACTAA[C/T]AGTTATTAAGCACCT	55159
rs372511878	snp	C/T	0.000116315	0.00762521	intron-variant	RFWD3	GRCh38.p7	16:74628688	GGAAAGTAAGGAAAC[C/T]GTATCTCACACTCCA	55159
rs372580730	snp	C/T	0.000153988	0.00877328	intron-variant	RFWD3	GRCh38.p7	16:74624109	AGGGTCAGGAGTCAG[C/T]CAGTACACGAAGGGA	55159
rs372631663	snp	C/T	1.71773e-05	0.00293059	intron-variant	RFWD3	GRCh38.p7	16:74652143	TACACAGAAAGACAA[C/T]GGAATTATAGTACAA	55159
rs372652567	snp	A/G	0.000201928	0.0100461	synonymous-codon	RFWD3	GRCh38.p7	16:74661423	TAACTGCACCTGAAC[A/G]TCATATTCCATTGCT	55159
rs372677015	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74634427	CCTCACTCTGTCACC[C/G]ATGCTAAGGTGCAGT	55159
rs372736909	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657149	CATATAAAGATAATT[A/C]TCTGGGAATGAGGCT	55159
rs372736984	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74638821	ATGTGGGCATGTTCT[C/G]AGAAACATGTTGTTA	55159
rs372749867	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648644	GGGCGGGGTGGCGTG[A/T]GCCTGTAGTCCCAGC	55159
rs372867524	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74644515	CTGACTTAACATGTT[A/C]ATGTGTCCTTACCTA	55159
rs372926679	snp	G/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621699	GGTTTTTTTTTGTTT[G/T]TTTGTTTTTTTTGAG	55159
rs372948163	snp	A/G	1.64743e-05	0.00287	intron-variant	RFWD3	GRCh38.p7	16:74644510	TCTGCCTGACTTAAC[A/G]TGTTAATGTGTCCTT	55159
rs373021544	snp	A/G	0.000153988	0.00877328	intron-variant	RFWD3	GRCh38.p7	16:74632487	CTACTCAACACCAAA[A/G]AGCCCAGTCTCCACC	55159
rs373065914	snp	C/G	4.94368e-05	0.00497152	missense	RFWD3	GRCh38.p7	16:74661260	GGGGTGGTGTCGCTT[C/G]GCTGCTGATCACCTC	55159
rs373068828	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74626674	TAAATGCATTAAACC[-/A]TCAAGAACAGTTACA	55159
rs373095908	snp	C/T	1.75953e-05	0.00296603	intron-variant	RFWD3	GRCh38.p7	16:74632707	TATGAAATAGATCAC[C/T]GAAAGTGAACCTAGG	55159
rs373128047	in-del	-/AGAT			intron-variant	RFWD3	GRCh38.p7	16:74666166	AAGAAAGACATAGAT[-/AGAT]TAGATAGACAGATTA	55159
rs373129903	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663290	AAGACTAAAGTCAGA[C/G]ACACTACTGTTAAAA	55159
rs373235113	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634731	ATCCTAGATTCAAGA[C/T]AGCTTCAGCTTCTCC	55159
rs373241885	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667092	AATCTACGTCCGTCA[C/T]CTTGCACCCGCCCCG	55159
rs373243733	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74628014	AGAGATGTTCAGCTG[C/G]CTGGGCACACACAGC	55159
rs373320915	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74645459	TAAATAAACCTAGAC[G/T]GTGTAAACTATTACA	55159
rs373422932	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635471	GACTCCATCTCAAAA[A/G]AAAAAAAAAAAATCA	55159
rs373499414	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627255	CCTGACTGTTACAAA[C/T]GTGTTTAATACAGTT	55159
rs373621395	snp	A/G	6.88338e-05	0.00586619	intron-variant	RFWD3	GRCh38.p7	16:74626561	GATTTTTATCTATGG[A/G]ACAGAGAAATCAGTG	55159
rs373621514	snp	C/G	1.64893e-05	0.0028713	missense	RFWD3	GRCh38.p7	16:74651923	TAAAATACTGACCTT[C/G]TAAAATGACAGCTCC	55159
rs373633204	snp	C/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74642922	TTTCTAATGAGGCTG[C/G]AGAGTATACTAATTC	55159
rs373638393	in-del	-/AAGACTCGGTAGTTA			utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666849	TAGTTACCTCGGCCG[-/AAGACTCGGTAGTTA]CACTCCGAATGCACC	55159
rs373690975	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74627954	AAAGAACCTGTGAAT[G/T]AAGCACAGTCTGCTG	55159
rs373703489	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74647127	GTACTGATAACAGAA[A/G]GCTCTCCAAGATGTA	55159
rs373781940	in-del	-/A	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74665325	GGCGCGGTGGCTCAC[-/A]CCTGTAATCCCAGCA	55159
rs373797136	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74630297	TAGAGACGGGGTTTT[A/G]CCACGTTGGTCAGGC	55159
rs373886910	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650873	CAGAGTGTAACCCTG[C/T]CTCAAAAAAAACAAA	55159
rs373895945	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74637146	AAAAAAAAAAAAAAA[A/C]AACTTAAAAGGAGAC	55159
rs373920982	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626917	GGTTTTTCCCTTCCC[C/T]CAGTGAGAACCTCAT	55159
rs373953511	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74649255	ATACAAAATAAGATA[C/T]GTCAGGTATGAGAAG	55159
rs374114527	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622437	CAAGACCAGCCTGGA[C/T]AACGTAGTGAAACAT	55159
rs374187275	snp	A/G/T	0.00176759	0.0296765	intron-variant	RFWD3	GRCh38.p7	16:74660920	CACAGACTTATCCAT[A/G/T]TATTTATTTACCTGG	55159
rs374207252	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637758	TTTCCTAAACAACTT[A/G]GCAAATCCTATTTGT	55159
rs374263739	snp	A/C/G	3.29458e-05	0.00405857	synonymous-codon	RFWD3	GRCh38.p7	16:74636419	ACAGTATGCCATGAT[A/C/G]CGGCAGTTTCCTGCC	55159
rs374297438	snp	A/G	0.000180901	0.00950884	intron-variant	RFWD3	GRCh38.p7	16:74624118	AGTCAGTCAGTACAC[A/G]AAGGGACTTCCATTC	55159
rs374299152	snp	A/C/G	3.30289e-05	0.00406366	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74624006	CACCTCAAATGGGCA[A/C/G]ATGTCCAACACAGGC	55159
rs374307348	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74633635	GATTATCAAAGGCCA[C/T]AGGGAAACTTTTGCG	55159
rs374312005	snp	C/T	0.000161115	0.00897393	intron-variant	RFWD3	GRCh38.p7	16:74624106	GGAAGGGTCAGGAGT[C/T]AGTCAGTACACGAAG	55159
rs374331584	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74653433	CCACAGAGAGTGAGC[A/G]AGCTATGGTTGTGCT	55159
rs374346913	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652597	TCTCTCATTTTAGGA[C/T]AGTATTTTTCTTTTA	55159
rs374347205	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74666522	CGCAGCAGCGAACTC[C/G]GCTCCTTCAGTGATC	55159
rs374374752	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658856	CACTGCAAGCTCCGC[C/T]TCCTAGGTTCAAGGA	55159
rs374472215	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639634	TTTTAATGCAATTTC[A/C/T]ATCAAGATCCCAAAG	55159
rs374473702	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74655364	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	55159
rs374480360	snp	A/G	1.64806e-05	0.00287054	missense	RFWD3	GRCh38.p7	16:74636531	GCTTGGGAGCCCCTG[A/G]GTTGCTGTAAATTCT	55159
rs374492324	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646517	AATTCGCTGGGCGCA[A/G]TGGCTCACACCTGTA	55159
rs374545270	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74625576	TCCAACCTTTTTTCT[C/T]CTGCCATTGACTTGT	55159
rs374574922	snp	A/G	0.000153988	0.00877328	synonymous-codon	RFWD3	GRCh38.p7	16:74651999	GTCACTGTCAGAATC[A/G]GAACTACTAGACACC	55159
rs374598389	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74630056	ATCACTTTTGATTAG[A/G]TTACCCTTAACTGAT	55159
rs374603917	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74642949	ATTCCTTATTGTAAT[C/T]AGTGAATTGTTTTTA	55159
rs374606493	snp	C/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74632650	TCTTCATGTTGGCAG[C/T]ACTCAACATCTTAAC	55159
rs374620621	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657570	AACATCCACCTCCCG[C/G]GTTCAAGCGATTCTC	55159
rs374624024	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74635831	AAAAGACTTGGTTTT[A/C]AACATTTAGAAAACC	55159
rs374625997	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74626821	AGAGAAAAACAATTC[A/T]GTGAGTTGTCTGTTT	55159
rs374645243	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662990	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	55159
rs374727394	in-del	-/CCAAAGAAACC			intron-variant	RFWD3	GRCh38.p7	16:74641955	AAAAAAAAAAAAAAA[-/CCAAAGAAACC]AAAAACCAAAACAAA	55159
rs374752623	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74626817	CTTAAGAGAAAAACA[A/T]TTCTGTGAGTTGTCT	55159
rs374762013	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74651799	TACTATAAAACAGGA[A/C]TCCACAACATTTAGG	55159
rs374771123	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664881	CTTTTCTCGTCGCAC[A/G]AAGTTCTATGGAACG	55159
rs374773782	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74651002	TTATTTACTRKTTTT[-/T]TGGAGTAATTAGTTG	55159
rs374830099	snp	C/T	3.36899e-05	0.00410412	intron-variant	RFWD3	GRCh38.p7	16:74628713	ACTCCAAAACTCGGA[C/T]GGCTCCAGACCCCAC	55159
rs374835291	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74629422	CCAGCACTTCGGGAA[C/G]CCGAGGTGGGAGAAT	55159
rs374838893	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627775	CCTGTGAAAGGCAAA[C/T]TATGAACACCCACAA	55159
rs374872724	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663948	AGCTTGACTCCTACT[C/T]AAACACCAGCCAGCT	55159
rs374875164	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74650393	GTGGGGGGCTGGTGT[C/G]TGTGTGTATACAGTA	55159
rs374982151	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625470	AGTGAGCCGAGATTG[C/T]GCCTCTGCACTCCAG	55159
rs375045262	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648256	ACACAAATAATGAGT[A/G]ACTGGGATAGGATCC	55159
rs375197409	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74650628	TGGGGGTCACAAAAT[A/G]ATGACTTTTCTATCG	55159
rs375210473	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621977	TTCCAAAACATCCAA[A/G]TTTAATGTACTAATG	55159
rs375271451	snp	A/G	1.64825e-05	0.00287071	missense	RFWD3	GRCh38.p7	16:74636354	TCTTTACCTGGAAGA[A/G]AAGAGGCCTGAGGAG	55159
rs375414530	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646889	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	55159
rs375443304	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74649986	ATATTTCTATCAGCC[C/T]ACAAAGATCCTTTAT	55159
rs375446216	in-del	-/GCA			cds-indel	RFWD3	GRCh38.p7	16:74623329	TGTTATTGCCACAAA[-/GCA]CACCCAGGTGTGCTA	55159
rs375452342	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74630595	ACTCTCCATCATATG[A/T]AATAGCATGAATACA	55159
rs375543700	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621537	AAGACATTTTGAGTT[C/T]GTTTAACTCCAAATC	55159
rs375575511	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74661678	TTTGCCCTTAGAAAA[C/G]ATGAAGTCCTGTGAT	55159
rs375645134	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627437	AAGGGAGCAGGCCTG[C/T]CCTGGATGGCTCCCC	55159
rs375652685	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74651348	CTAGGCCGGGTGCAG[C/T]GGCTCATGTCTGTAA	55159
rs375666291	snp	C/T	1.64738e-05	0.00286995	missense	RFWD3	GRCh38.p7	16:74651977	CCCCTCCATACTCTG[C/T]AGAGCTGTCACTGTC	55159
rs375788482	snp	A/C	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74647822	GTCTTGAACTCCTGA[A/C]CTCAGGTGATCCGCC	55159
rs375812818	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74657498	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGC	55159
rs375885726	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645520	ACTGTACCAAATACT[A/G]TAGGCAACTGTAGCA	55159
rs375910589	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662098	TTCCTATCTTTAATT[C/T]CATTGTATCAGTTTG	55159
rs375919519	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663078	CCTGGCTAATTTTTT[A/G]TATTTTTAGTACAGC	55159
rs375943061	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74659949	CCAGTTAATCATCAA[C/G]AGGCTGAGGTAGGAA	55159
rs375957099	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656559	ATGATATTGGCTCAT[C/T]GGAACCTTTCACCCC	55159
rs375986240	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74629673	CCACCAACAAAAAAA[-/A]AAAACCTTGCCATAT	55159
rs376013346	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645402	ACATTCTGAGAAATG[C/T]GTCTTTAGGCGATTT	55159
rs376027907	snp	C/T	8.24368e-05	0.00641963	missense	RFWD3	GRCh38.p7	16:74623986	GCCAAGTAGCTGTTA[C/T]GGTTCACCTCAAATG	55159
rs376032009	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638997	CTATAATGGTATTTA[C/T]GTATCTAAACATAGA	55159
rs376034269	in-del	-/AAAAG			intron-variant	RFWD3	GRCh38.p7	16:74628995	GTTTAGCCACATAAG[-/AAAAG]TCAGAAAAGAAACAA	55159
rs376045953	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74637833	ATTCCAAAAGTTCTT[G/T]GGATTAGAAAGGACA	55159
rs376054494	snp	G/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621700	GTTTTTTTTTGTTTG[G/T]TTGTTTTTTTTGAGA	55159
rs376060878	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74665556	GCACTCCAGCAGGGG[A/C]AACAAAGCGAGACTC	55159
rs376133334	snp	A/G	3.63036e-05	0.00426034	intron-variant	RFWD3	GRCh38.p7	16:74630738	ACAATAATAAGCCAA[A/G]AGAAAGCTGCTACCA	55159
rs376158512	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668744	AACTTGGTCTTGTAT[G/T]TTTAGTAACTGTGTT	55159
rs376262888	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74658685	CCCTTTGTGGAGACA[-/A]GATTATGGCTGCCAA	55159
rs376263170	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642626	TCTCCTGAGTAGCTG[A/G]GACTACAGGTGTGTA	55159
rs376347902	snp	C/T	6.68304e-05	0.0057802	intron-variant	RFWD3	GRCh38.p7	16:74636296	AGGCAAGGAAATAAA[C/T]ATATGGAGTCTAATA	55159
rs376483833	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74654051	TTAGCATAACCACAA[C/G]GTTATGTAATCATAA	55159
rs376486040	snp	A/G/T			intron-variant	RFWD3	GRCh38.p7	16:74653871	AATAAACACTACTCA[A/G/T]TGTCCAACTCAATAG	55159
rs376521680	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74647622	TTTGAGATGAAGTCG[A/T]GCTCCGTCTCCCAAG	55159
rs376562898	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74628208	TAGGGGCTCCTAAGT[A/G]GCTAATTCACTTCCA	55159
rs376585995	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622782	CAAGGCAAAGAAATA[C/T]AAACTGAGCCCTAGA	55159
rs376610962	in-del	-/GTTTGG			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667140	TTTTGTTTTTTTTTT[-/GTTTGG]TTTTTTTTTTTTTTT	55159
rs376643768	snp	G/T	1.73042e-05	0.00294139	synonymous-codon	RFWD3	GRCh38.p7	16:74637867	GTACCTGAACACGCC[G/T]TTGAAGCCTAGTGCA	55159
rs376662428	in-del	-/AAAAC			intron-variant	RFWD3	GRCh38.p7	16:74632394	AGACTCCATCTCAAA[-/AAAAC]AAAACAAAACAAAAC	55159
rs376675648	snp	C/G			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74661989	CTGAGCAAACTTTAT[C/G]CTATCCCTTTCATTA	55159
rs376703465	snp	C/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74644663	ACTGTTCCAGACATA[C/T]TGTACAAGTGTCCCC	55159
rs376761731	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74640733	TCACGAGGTCAGGAG[A/T]TCAAGACCATCCTGG	55159
rs376763470	in-del	-/TAACTGGA			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622870	AAGGCTTTAACTGGA[-/TAACTGGA]ATGTATAAAGAACAC	55159
rs376766703	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629501	CCATCTCTACTAAAA[A/G]TACAAAAGTTAGTCA	55159
rs376769438	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74641740	CCAGCCTGGCCAACA[A/C]GGTGAAACCCTGTCT	55159
rs376800358	snp	C/T	0.000182447	0.00954936	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623917	ATGCCTTCAAGGTTT[C/T]GAGACCACAGTCACT	55159
rs376863355	snp	A/C/T	1.8448e-05	0.00303705	intron-variant	RFWD3	GRCh38.p7	16:74626581	AGAAATCAGTGCTGC[A/C/T]CCATGGGGACGCTAC	55159
rs376866995	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656580	CTTTCACCCCAACCT[C/T]CTAAGTAGCTGGGAC	55159
rs376882650	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74626819	TAAGAGAAAAACAAT[A/T]CTGTGAGTTGTCTGT	55159
rs376883754	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74656953	TTAGAAGATGTGACT[C/G]AATTGATCTCATTCC	55159
rs376995214	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74633714	CAGCACTTTGGGAGG[C/T]TGAGGTGGGTGGCTC	55159
rs377017032	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623371	TGTGTGGAGATGAGA[C/G]AAGTTACTAAAAGAT	55159
rs377102043	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655350	GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCCG	55159
rs377106282	snp	A/G/T			intron-variant	RFWD3	GRCh38.p7	16:74640550	CCTGTACTCCCAGCT[A/G/T]CTCAGGATGCTGAGG	55159
rs377155984	snp	C/G	9.92802e-05	0.00704487	intron-variant	RFWD3	GRCh38.p7	16:74632498	CAAAGAGCCCAGTCT[C/G]CACCTACTTCCCCAA	55159
rs377164399	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639109	AGTGGCGTGATCCAG[A/G]CTCACGGCTACCTCC	55159
rs377170837	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667047	GACGAGGCGGGACCG[C/T]GCTTGAGGAAGCCTC	55159
rs377173129	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74661143	CATCAGATCCCTGCC[C/T]ATGTTGTTCTGAAGT	55159
rs377197480	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646487	ACCATGCTTTACATG[A/G]TAAGAAAAAGAATTA	55159
rs377204072	in-del	-/CT			intron-variant	RFWD3	GRCh38.p7	16:74665748	GACTTTTCTTTCTTT[-/CT]TTCTTTCTTTTTTTG	55159
rs377256969	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632334	AAGGTGGAGCTTGCA[A/G]TGAGCCGAGATCCCA	55159
rs377304819	snp	C/T	1.65244e-05	0.00287436	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630819	CTGCACATGACTGCT[C/T]GTGTTTCGCACGTCA	55159
rs377336147	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664004	TCTCCCCCTATGCAC[A/G]AGAAAACTGGAGGTT	55159
rs377365468	snp	C/T	1.66073e-05	0.00288156	missense	RFWD3	GRCh38.p7	16:74632659	TGGCAGTACTCAACA[C/T]CTTAACACCAAAGCC	55159
rs377434688	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667880	TGATTCTGACAGATA[C/T]GGTGAAAATGAAGAA	55159
rs377488038	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663701	AAACAGGGTATGATA[C/T]GCAAACCAGTTTTTT	55159
rs377611366	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74653319	TCCAGCCTGGGTATC[A/T]GAGTGAGACTTGTCT	55159
rs377673527	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622478	AAAAAAATTTAAAAA[A/G]GGAAAAAATTATGTC	55159
rs377720830	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649468	TCAATTTAAAAAATA[A/G]TCAATATTTTGCCAA	55159
rs377742879	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643888	TTCACCGTGTTAGCC[A/G]GGATGGTCTTGATCT	55159
rs386364851	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74658767	GAGCAGATTCTATAA[-/TT]TTTTTTTTTTTTTTT	55159
rs386385073	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74650999	CCTTTATTTACTAGT[-/T]TTTTGGAGTAATTAG	55159
rs386385075	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74657492	CTTTTTTTTTTTTTT[-/TT]TGAGACGGAGTCTCG	55159
rs386792117	multinucleotide-polymorphism	GCC/TCG			cds-indel	RFWD3	GRCh38.p7	16:74666843	GACTCGGTAGTTACC[GCC/TCG]GCCGCACTCCGAATG	55159
rs397696290	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74625213	CAAAAAAAAAAAAAA[-/A]GTAGAGAGGGACAGA	55159
rs397732816	in-del	-/A	0	0	intron-variant	RFWD3	GRCh38.p7	16:74625527	AGAAAAAAAAAAAAA[-/A]GGACAGACCAGGCGC	55159
rs397757816	in-del	-/A	0	0	intron-variant	RFWD3	GRCh38.p7	16:74633293	GAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAAG	55159
rs397795043	in-del	-/A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74659611	AAAACAAAAAAAAAA[-/A/G]CCCAGAGTAATATGC	55159
rs398058371	in-del	-/CAT			intron-variant, cds-indel	RFWD3	GRCh38.p7	16:74662031	CATCTCTAATTCCAT[-/CAT]GTTAGCGTATTCAAC	55159
rs398078751	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74635482	AAAAGAAAAAAAAAA[-/A]ATCAACAAGGTAACA	55159
rs398078752	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74644830	CAGAAGTGCAAAAAA[-/A]ATGATACAATCAAAA	55159
rs527261330	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666299	GTTTCCTAAACTCGG[C/T]TCAACTTGTTCTCCT	55159
rs527312027	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628380	CACCCAAAGGGTAGG[A/C]TCAAACCCTCCTTCC	55159
rs527342780	snp	C/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668489	TGAGGATGGAGGAGT[C/G]GTTTTCATCTACATA	55159
rs527390477	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639222	TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC	55159
rs527419182	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634221	CAGTCAAGATATGTC[A/C]CATCTGTCTGAAATG	55159
rs527420201	snp	A/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74666000	ACCGCTTTTCTCTTT[A/T]TAACACCTTTTTCTC	55159
rs527422641	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74627723	TCTGGTCATGGGTCA[A/G]GCAGGCATTAGGCCA	55159
rs527485063	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74638812	AGCTTAATGATGTGG[C/G]CATGTTCTGAGAAAC	55159
rs527505597	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74648539	GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC	55159
rs527565000	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648836	CATGACTACAATCTC[A/G]ATGGTTTGGGAGGCC	55159
rs527574332	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663559	ATTCTAATAAACATA[A/G]TGGACGAAGTACATA	55159
rs527656202	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74654917	TTCTGTGAAAGCTGA[C/G]AAGTGAGGAAGCTGC	55159
rs527717574	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655278	AGAGTCTCACTTTGT[C/T]GCCCAGGTTAGAGTG	55159
rs527835445	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621001	AAAAAAAAAAAAGGC[C/T]GGGTGCGGTAGCTCA	55159
rs527903276	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625972	CGGCAGATCACTTGA[A/G]GTCAGGAGTTCCAGA	55159
rs527908200	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633042	AGCACTTTGGGAGGC[A/C]GAGACAGGTGGATTA	55159
rs527932432	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665170	ATCTTTGCTCTGGCC[A/G]GTGCAGAGGGTCACG	55159
rs527935516	snp	C/G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659695	TACAGACACTGGAGC[C/G/T]ACAGTCATGGCAAGC	55159
rs527943180	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668843	AGTATTCCATTGGAA[A/T]GCAAACAAAAGATAT	55159
rs527948420	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74648436	CTGGGATTACAGGTG[G/T]AAGCCACCGTGCCCA	55159
rs527986783	snp	A/G	8.47063e-05	0.00650738	synonymous-codon	RFWD3	GRCh38.p7	16:74637907	GAGGACCTGCAGTTG[A/G]AGTCGGCACTGTGCT	55159
rs528125794	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652355	GAGCTTGATCCTTCC[A/G]TTAAAAGCTAATTCT	55159
rs528149183	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655721	GTGGAGACGGGGTTT[C/T]ACCGTGTTAGCCAGG	55159
rs528184434	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657693	TGGCCAGGCTGGTCT[C/G]GAACTCGTGACCTCA	55159
rs528199741	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654214	TCTCTATTTCTTGGT[C/T]GGTCTAGCTAAAAGT	55159
rs528302589	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623731	AGTACCCATCAATTA[C/T]TCTTTTAGTGGACAT	55159
rs528335202	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657295	GCCATAGAGCTCAAT[C/G]AGATTCGGCTGTTTT	55159
rs528373794	in-del	-/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666982	TCTTCTTCAATGGGT[-/C]CCCCCGATAGCTGAA	55159
rs528453472	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639996	TATTATTGTTAATCT[C/T]TTACTGTTCCTAATT	55159
rs528481928	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640461	AAACTTAATTAAGGA[C/T]AGAAGTAGCAATGAA	55159
rs528499794	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635017	CGGGCGCGGTGGCTC[A/G]CGCCTGTAATCCCAG	55159
rs528565911	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645279	CTGGAGCACCATTTG[C/G]CATTATCCATGAAAA	55159
rs528634336	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656624	ACCATGCCCAGCTAA[A/T]TTTTGTATTTTTTTG	55159
rs528694610	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74650041	TGCATCTGCAGCCCT[A/G]GGCAACCACTAATAT	55159
rs528744336	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622441	ACCAGCCTGGACAAC[A/G]TAGTGAAACATCTAT	55159
rs528798863	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74625098	CCAGCTACTTGGGAG[A/G]CTGAAGCACAAGAAT	55159
rs528863377	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657186	GTGCTCCAATCCCTC[C/T]GGTGCCTGCCAGGCT	55159
rs528901984	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74627927	AATTTAGATTCATGC[C/T]GCTTAGCCTAGAAAG	55159
rs528913866	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650980	AATATTAATATATTC[C/T]TGACCCTTTATTTAC	55159
rs528943740	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74630166	AACGGCGCAATCTCG[A/G]CTCACCGCAACCTCC	55159
rs529003825	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656771	GGGATCCACCATCCT[C/T]GATGCCCCTAAGAAC	55159
rs529023673	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623667	AATTTCCAACATACA[A/G]TAATGGTTAATGAAG	55159
rs529062287	snp	A/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622131	GGCCCAAAGACAAAG[A/C]CAGCCAGGACCTGAC	55159
rs529109971	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74629463	CACCGGTTTGAGACC[A/G]GCCTGGCCAATATGG	55159
rs529118863	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667276	TATCCCTAACGCTTT[A/C]GTGAAGGAGTTATCT	55159
rs529142700	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661740	ATAAACCAAGGAGAT[G/T]AAACTACTGGGTCTA	55159
rs529200768	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639913	TCGAGATATGTTGAG[A/C]GAGAGATGGAGACCA	55159
rs529240135	in-del	-/TA/TATA	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74630097	TGCTAGACATGTGGC[-/TA/TATA]TATTTTTTTTTTTCT	55159
rs529259359	snp	C/T	6.59554e-05	0.00574224	missense	RFWD3	GRCh38.p7	16:74644645	GGTCCCCAGCATTGG[C/T]CCACTGTTCCAGACA	55159
rs529312861	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639322	GGATTACAGGTGTGA[C/G]CTACTACACCCAGTG	55159
rs529380483	snp	C/T	1.65102e-05	0.00287312	intron-variant	RFWD3	GRCh38.p7	16:74649253	AAATACAAAATAAGA[C/T]ATGTCAGGTATGAGA	55159
rs529405838	in-del	-/AA	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658740	ATTTAAATTCTGTAT[-/AA]CTCATTCCCTGAGCA	55159
rs529414913	snp	C/G	4.94181e-05	0.00497057	missense	RFWD3	GRCh38.p7	16:74661163	TGTTCTGAAGTTCTT[C/G]GATTGATGTTCTCCA	55159
rs529415671	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74644001	GTTTTGTGCTTCCGA[A/C]ATCCTGGTAATTTTT	55159
rs529475421	snp	C/G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74656037	TAATATAACATATTC[C/G/T]GCAGCCCAACTTTCA	55159
rs529502426	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664674	GAACCCCTTGAACCC[A/G]GAGAGTGGAGGTTAC	55159
rs529508882	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648862	AGGCCGAGGCAGGAC[G/T]ATACCTTGAGCCCAG	55159
rs529512648	snp	C/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663254	AAACCACCTGAGGAA[C/G]AGAATGACAGAAGAG	55159
rs529520314	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643937	CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC	55159
rs529546597	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74660641	TGGGTGAGTAGAGAC[C/T]TGCAAGTGAAGAAAG	55159
rs529549317	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74627668	GACAAGAGCCACAAG[A/G]GTACCTGCCAGTACA	55159
rs529698689	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74642672	AATTTTTTTCATTTT[C/T]ATTAGAAACAAGGTC	55159
rs529806431	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658928	GTGTGCCACCACGCC[C/T]GGCTAATTTTTTGTA	55159
rs529808507	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652757	TTAAAATAACCACTA[C/T]TGTACCTCAGTTTCT	55159
rs529909100	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624635	CTCCTGACCTCAGGT[A/G]ATCCACCCACCTTGG	55159
rs530005288	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664074	AGTACTGAAAATAAG[C/T]GGGAAAGAAAGTCTG	55159
rs530026119	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668297	ATACCCAGAAGAACA[C/T]CAAAGAAACCATTGA	55159
rs530048805	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625126	AATCACTTGAACCCA[A/G]GAGGTGGAGGTTGTA	55159
rs530059812	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74631305	CCTGGCCAACATGGC[A/G]AAACTAAAATACAAA	55159
rs530085582	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663498	CAGTTTCCCTGAAGT[A/G]GTGGGGTCAGAGGCC	55159
rs530129434	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641755	CGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA	55159
rs530130435	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74624240	TCAGCACACCTGACA[C/T]AGTTCAGGTACAGCC	55159
rs530200927	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640644	CAAGACCCTGTCTTT[A/T]AAAAAAATTTTTTGG	55159
rs530204438	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646405	TAGCATGATTTATAT[A/C]AAGAAAAAAAATATT	55159
rs530232508	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667858	ATACAAGGCAGAATG[C/G]AAGTAATGATTCTGA	55159
rs530241443	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74641189	TTTTTGAAGACAGAG[C/T]TTCGCCATTGTTGCC	55159
rs530244784	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74630707	CTGTGGAACACCCAC[C/T]GAAGAGACGATTAAC	55159
rs530316783	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642200	CAATCTCAGCTTACA[A/G]TAACCTCCGCCTCCC	55159
rs530402561	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645884	CAGCCTCCTGAGTAG[C/G]TGGGACTACAGGCGC	55159
rs530408494	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74631582	GCACACTCACATCTG[G/T]TTCACAGTACTCACA	55159
rs530445787	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74630158	TGGAGTGCAACGGCG[A/C]AATCTCGGCTCACCG	55159
rs530492137	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646858	CGGGCGGATCACCAG[A/G]TCAGGAGATCAAGAC	55159
rs530531070	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74647474	TGTATTTTTAGTAGA[C/G]ATGGGGTTTCACCCT	55159
rs530549125	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74635989	TTAAATTTTGTTTCA[C/T]CTTGAATTAACCCTT	55159
rs530582438	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663386	TGTCTTGGAAAAACA[A/G]TGTTTCAAGGAAGGA	55159
rs530619533	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74637648	AAAAAAATAAAAAAT[A/T]AAATTCAGACTATAG	55159
rs530635820	snp	C/G/T			intron-variant	RFWD3	GRCh38.p7	16:74655821	GTGAGCCACCACACC[C/G/T]GGCCTATGTCTGTGC	55159
rs530643743	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658239	CTGTGTTATTCACCA[A/G]TATATCTAGGGCAAA	55159
rs530697394	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74657758	CGATTACAGGTGTGA[A/G]CCACTGCGCCTAGCC	55159
rs530704690	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630607	ATGAAATAGCATGAA[C/T]ACAAACTCTTATTAA	55159
rs530715297	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662986	CTCGGCTCACTGCAA[G/T]CTCCGCCTCCCGGGT	55159
rs530778474	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74641095	CATTGCTAGACCTCT[C/G]TGCAGCATGGCTAAT	55159
rs530787263	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74654620	AGTCAGGCATCTCTC[A/G]CTTTAAATCACTAAG	55159
rs530828360	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74640424	GCTGGGATTACAGGC[A/G]TGAGCCAATGCGCCC	55159
rs530828830	snp	C/G	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662575	GTACTCTTTTAAAGA[C/G]TGAAAATTGGGCTGA	55159
rs530856707	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624146	TTCTTCATCATCTAA[A/C]AAGTCTGAAAGGCTG	55159
rs530899788	snp	A/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74635389	GGAGAATCTCTTGAA[A/T]CCAGGAGGCAGAGGT	55159
rs530957305	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74650911	AAAAACAACAAAAAA[A/C]CCCACTTCATCAACT	55159
rs531186169	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665370	GGGCAGACCACTTGA[G/T]GTCGGAGTCCCAGAA	55159
rs531340123	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638679	AGCAACGCTGCTGGA[C/T]TCAAGACCAAAAAAA	55159
rs531359748	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633741	GCTCGCTTGAGATCA[G/T]GAGTTCGAGACCAGC	55159
rs531375596	snp	A/G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642913	TCTTCACTTTTTCTA[A/G/T]TGAGGCTGGAGAGTA	55159
rs531412304	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643698	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	55159
rs531632412	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74657913	ATCAAATACATACTA[C/G]AGTTAGGGTGTTGAC	55159
rs531636138	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654146	CAGTCATTTCCCCTC[C/T]TATTTGGTAGTCATG	55159
rs531663373	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641858	TTGAACCTGGGAGGC[A/G]GGAAGTTGTAGTGAG	55159
rs531702929	snp	A/C	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74659561	TACTGCGCCACTGCA[A/C]TCCAGCCTGAGTGAC	55159
rs531742401	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647973	ATTTTTTTATTGAGA[C/T]AGGGTCTCACTCTGC	55159
rs531843619	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664743	GAGAGAGTAAGACTC[C/T]GTCTAAAAAAAGAAA	55159
rs531847522	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658980	CACCATGTTGGCCTC[A/G]AACTCCTGGCCTAAA	55159
rs532002475	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74666174	CATAGATAGATTAGA[C/T]AGACAGATTAGATAG	55159
rs532029323	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636839	CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACATG	55159
rs532036565	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74651579	AGCTGAGATTGTTGT[C/T]GCTGCACTCCAGTTG	55159
rs532127682	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647612	ATTACTATTCTTTGA[A/G]ATGAAGTCGTGCTCC	55159
rs532386553	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664153	GATGGGGTTTCCCAC[A/G]TTGCCTAGGCTGGTC	55159
rs532451218	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658965	GTAGAGATGGGGTTT[C/T]ACCATGTTGGCCTCG	55159
rs532463853	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631431	TGAGCTAAGATCATG[C/T]CACTGTACTCCAGCC	55159
rs532564551	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641799	GGCATGGTGAAAGGC[G/T]CCTGTAATCCCGGCT	55159
rs532601671	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636707	ATGAATCCTAGAGAA[C/T]TGCAGAGTTTTTGTT	55159
rs532632263	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74637141	AAAAAAAAAAAAAAA[A/C]AAAACAACTTAAAAG	55159
rs532676662	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668655	TATGGAAACCAACCA[C/T]GTAAATCCCTTCTCT	55159
rs532726005	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633528	TAACACTATATAATT[C/T]CATTTATGTAAAATT	55159
rs532784268	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623060	ACTCAAGTAAAAGCT[C/T]TGACCTATCACTCAT	55159
rs532818479	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641220	CAAGCAGGAGTGCAA[C/T]GGTGCGACCTCGGCT	55159
rs532873924	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74634900	TAATCCCAGTACTTT[C/T]GGAGGCTGAGATGGG	55159
rs532922136	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661691	AACATGAAGTCCTGT[A/G]ATCATAGTAGTATCT	55159
rs532935692	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74665026	TTTATGTGTGCTGTG[A/G]GCGGTGCTTAAAATG	55159
rs533054419	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74638923	AAGCTATATACTGTT[A/G]CTCCCAGGCTACAAA	55159
rs533062651	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666857	CTCGGCCGCACTCCG[A/G]ATGCACCTACGCCAA	55159
rs533062966	snp	A/C/G/T	4.98306e-05	0.00499133	missense	RFWD3	GRCh38.p7	16:74661355	TGGAGGAGGGCTGGT[A/C/G/T]CCCCTTGGCTGCTGG	55159
rs533102164	snp	C/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74647018	TGTGAACCTGGGAGG[C/T]GGAGCCTGCAGTGAG	55159
rs533133318	snp	C/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664025	ACTGGAGGTTTGAAC[C/G]ACACAGGCTTACACT	55159
rs533179701	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643757	TTCGGCTCACTGCAA[A/G]CTCTGCCTCACGGGT	55159
rs533194844	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622953	GAACTCTCAAAATGG[A/G]AGACAAGTTCTTCTC	55159
rs533221079	snp	C/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74658190	CTCTCTGTAGTCCTA[C/G]ACTCCGTATGCTCCA	55159
rs533277378	snp	A/T	0.0023933	0.0345097	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666957	CCTACGCTGTGGCCA[A/T]TACCCACTCTTCTTC	55159
rs533375910	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621122	TCTCTACTAAAAATA[A/C]AAAAATTAGCCGAGC	55159
rs533403261	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644049	GCAAAGCTTCACTTA[C/T]GAGTTTTCTGTATGG	55159
rs533447416	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665298	ACCAAAAAAGAAAAA[C/T]AGAACAGGTCAGGCG	55159
rs533539801	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660708	CAATCTCTACAGAGA[C/T]TGCCAACAAACTACC	55159
rs533569899	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648665	TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGTAGG	55159
rs533579021	snp	C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74627385	AGGTTTGAAATATAG[C/T]CCACTTGTCCCTCCC	55159
rs533623956	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660487	CAAAAAACGGACAGG[G/T]TATAGGCAATTGTTA	55159
rs533655945	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633191	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	55159
rs533705807	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632848	TTATTTTTGAGAGTT[A/G]GCCAGGCTGGAATGC	55159
rs533743317	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633356	GAAGAAGAAAAAAAA[A/G]AAGAAAAAGTATAAC	55159
rs533747293	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74664967	GAACGAGAGACCATG[A/G]GCTGGGCACCCCAAA	55159
rs533815079	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638041	CATCCAGGTGGCAGA[C/G]TTAAGTTCATGCTAT	55159
rs533847084	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74665421	CGTCTCCACTAAAAA[C/T]ACAAAAACTACCCGG	55159
rs533894364	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642502	GACCTGGTCAACAGA[C/T]TTATCTTTATTTTTT	55159
rs533927687	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663596	TCTTTCTCTCTCCAC[C/T]CCAGTCATTCCTAAA	55159
rs534050266	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647667	CGCTATTTGGGCTCA[A/C]TGCAACTTCTGCCTC	55159
rs534117982	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74635003	TAACTAGGCATAGCC[A/G]GGCGCGGTGGCTCAC	55159
rs534151709	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74647950	TGCCTGATTTTTTTT[A/T]AATTTTAATTTTTTT	55159
rs534242148	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642941	GTATACTAATTCCTT[A/T]TTGTAATCAGTGAAT	55159
rs534278069	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74642477	ATTTTCTTTCCTTTT[C/T]TTCCTTCTTGACCTG	55159
rs534359432	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74633289	CTCAGAAAAAAAAAA[-/G]AAAAGAAAAGAAAAA	55159
rs534438760	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632243	CAAAAATAGAAAATA[C/T]TAGCCAGGCATGGTT	55159
rs534439663	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653443	TGAGCGAGCTATGGT[A/T]GTGCTACTGCACTCC	55159
rs534455800	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628065	TGCCAGCCGGGCTAC[C/T]ACATGGCTGCCCTAA	55159
rs534492740	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632175	GCGGGCGGATCATGA[A/G]GTCAGGAGATTGAGC	55159
rs534503848	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656895	CAAGACTTCAGTTAA[C/G]AAAGTAACTGCAGAT	55159
rs534521820	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74630547	TTTGCCATGTTAGAT[C/G]ATTACTATGAACCTG	55159
rs534527121	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664426	TAGGGGGCCGCACTG[C/T]CTACTCCCATATGGT	55159
rs534543002	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625377	AATACACAAATTAGC[C/T]GGGTATGGTTGGTGT	55159
rs534558667	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74649825	TCACCCATTTTTTTC[C/T]CCTCTGTTTGTCATT	55159
rs534562782	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640303	GGTGTGTGCCACCAC[A/G]CCCAGCTAATTTTTG	55159
rs534636282	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661914	AAGGACATTTTTTAC[A/T]CTTGCAAAATTAACT	55159
rs534717194	snp	A/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74651061	ATGAGGTTTTGGAAA[A/T]TTATATAAATATGAA	55159
rs534730650	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74645573	GGCCGGGCTGGTCCC[A/G]AACTCCTGACCTCAA	55159
rs534787391	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639396	ATTTTCAGCTCCATT[A/G]TAATCTTATGGGGCC	55159
rs534862691	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74650398	GGGCTGGTGTGTGTG[C/T]GTATACAGTACTTCC	55159
rs534872856	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74631917	GAGCCACCACGCCTG[C/G]TCTCCACCAACTTTA	55159
rs534878388	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661550	GATTTTATGTTTAAT[A/G]TCATTCTTAGCAAGA	55159
rs534905668	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622852	CATCAGCTTCACATG[A/G]GGAAGGCTTTAACTG	55159
rs534908899	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629529	TCAGGTGTGGTGGCA[C/T]ACGCGTATAGTCCCA	55159
rs534940539	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656444	TTCCTCTAATGGATC[C/T]GGACAAAGTAAATTG	55159
rs534946963	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644785	AAATGTAAAATCAAT[C/T]TTGAAGAAGATGTGC	55159
rs535000855	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648915	TATAGTGAGACTCTG[C/T]CTACAAAAAATAAAA	55159
rs535021585	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643878	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	55159
rs535071191	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74634832	GGGGGGAAGGGGGGC[A/G]CAGGTATAGGCTTTA	55159
rs535111324	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668637	GTGTTTGGTCTATCA[A/G]GCTATGGAAACCAAC	55159
rs535124636	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639497	AGGCAGGATCTTTAT[A/G]AAGCAAAATACACTT	55159
rs535148416	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645492	CTTAGACAACAAACC[C/T]GTATAGGATGTTACT	55159
rs535174057	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644246	AATGATCCCCAGAGA[C/T]CCCAAGTCACAGGTC	55159
rs535254738	snp	C/T	8.23608e-05	0.00641667	missense	RFWD3	GRCh38.p7	16:74644420	TTCGGGCATAAAGGA[C/T]GACAATGTCACTGTG	55159
rs535263423	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639095	CTAGGCTGCAGAGCA[A/G]TGGCGTGATCCAGGC	55159
rs535386745	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645038	AATATTTAACTCATG[G/T]GTACCAGAGGGCAAA	55159
rs535406259	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74666487	GCCGGGCGACCTCCC[A/C]CCCCGGCCAGGGCAG	55159
rs535450907	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633511	GTCAGACCAAAAAAT[A/G]GTAACACTATATAAT	55159
rs535542288	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649497	AATCTTGTTCCACCT[A/G]AGCCCCCATTCCATT	55159
rs535581496	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623376	GGAGATGAGACAAGT[C/T]ACTAAAAGATTGTCA	55159
rs535627727	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655777	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	55159
rs535638623	snp	A/C/T	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74661733	AAGATCTATAAACCA[A/C/T]GGAGATTAAACTACT	55159
rs535668567	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621291	CAAAAAACAAACAAA[C/T]GAACAAACCCGAGAA	55159
rs535699108	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666197	TTAGATAGATAGATA[A/G]ATAGATAGATAGATA	55159
rs535739542	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627982	CTGTTATGCGTTCCA[C/T]CTCTGATTCCAGAGG	55159
rs535792356	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648146	AGCACATTTATGTCT[A/G]TTTTTTCAACTGATA	55159
rs535860664	snp	C/T	0.00835141	0.0640778	intron-variant	RFWD3	GRCh38.p7	16:74636677	ATTTTTTATCCATTA[C/T]ATGAAAGTGTTAACA	55159
rs535864386	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668389	GAAATGTTCCCCTAT[A/G]AAGCAACTACACCAA	55159
rs535923837	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646813	CATGGTGGCTCACGC[C/T]TGTAATCCCAGCACT	55159
rs535937208	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644154	GTGTTTAATGCTCTA[C/G]ATAAGGCAAACGATG	55159
rs535937233	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638479	GTATCATAAAAGGAC[A/G]CATTCACCAAGAATA	55159
rs536002684	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648640	AGCTGGGCGGGGTGG[C/T]GTGTGCCTGTAGTCC	55159
rs536006166	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74666660	CCTCAGGCCGCCGGG[A/T]TCCAAGCCCGCGTGC	55159
rs536015354	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646584	TGAAGTCAGGAGATC[A/G]AGACCATCCTGGCTG	55159
rs536100188	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74641316	TACAGGTGCGTGCCA[A/C]CATGCCCGGCTAATT	55159
rs536113077	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621245	TGGCGCCACTGCACT[A/C]CAGCTAGGGCTACAG	55159
rs536151078	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655078	CAATTGATGAAAGTA[C/T]CTACACTAAAAAGAT	55159
rs536262353	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74631742	TAAACAGTACCAACC[C/T]GGTATGGCGACTCTG	55159
rs536291264	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657791	GTTTTCTTTTTAGAC[A/G]GTGCTAAGCAAGTTT	55159
rs536306724	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667546	GAAAGGGGCCCCCGG[A/C]ATTCTCCAGCTACGT	55159
rs536331945	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636274	TTTGAGTCTTGAATT[G/T]TCCAAAAGGCAAGGA	55159
rs536343069	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630292	TTCAGTAGAGACGGG[A/G]TTTTACCACGTTGGT	55159
rs536384212	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668022	CTGGAATAACTGGGA[C/T]TGAATGGACAAGTGG	55159
rs536387744	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645419	TCTTTAGGCGATTTC[A/G]TCATTGAATGATCCC	55159
rs536456975	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635562	CAGCACACTATCAAG[C/T]GGACTGGAATGGACA	55159
rs536531324	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640203	GTTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC	55159
rs536565336	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646162	GGAGGATTCCTTGAG[A/C]TCAGGAGTTTGAAAC	55159
rs536633603	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74650232	TTCCATTTGTAGACT[A/G]TTCTACATTTTTAAT	55159
rs536695571	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651222	GGGGTCTCTGCCTAC[A/G]ACTATTAAATAAAGT	55159
rs536714739	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668562	TACAAAAAAAAGGGA[C/T]GCTCCATTCCTGTAT	55159
rs536749558	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623386	CAAGTTACTAAAAGA[G/T]TGTCAGCCTTCAAGG	55159
rs536847596	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667044	CCTGACGAGGCGGGA[C/T]CGCGCTTGAGGAAGC	55159
rs536861817	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74629832	TTCAGATTTTGGCCA[A/G]GTCACAGACCCTACT	55159
rs537016378	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74641288	CTGCCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC	55159
rs537023396	snp	A/G	0	0	intron-variant	RFWD3	GRCh38.p7	16:74635747	GTCTTGCAGTTGGCA[A/G]AAATCTTATGCTAAA	55159
rs537085655	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662491	ACAAATACATGAAAA[A/C]AATTATAGATTATGA	55159
rs537102367	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74666719	CCCAATCCAGGAATC[A/G]GGCGTGGGGAGGTTT	55159
rs537128611	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646535	GCTCACACCTGTAAT[C/G]CTAGCACTTTGGGAG	55159
rs537147721	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635083	CAGGAGATTGAGACC[A/G]TCCTGGCTAACACGG	55159
rs537185292	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74642778	GATTACAGGCATGAG[C/G]CACTACACCCAGCCT	55159
rs537259127	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74640077	TCAGGCATTCACTGG[A/G]GGCTCTTGAAATGTA	55159
rs537335639	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644935	TATGAAAACTATACT[A/C]CTCTTAAATCTTATA	55159
rs537428481	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659776	ACAGAAGGCACAATT[C/G]CAATTCCAGCCTTAT	55159
rs537464033	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623354	GTGTGCTATCACACA[C/G]TTGTGTGGAGATGAG	55159
rs537490857	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660111	GGGATTTCGTCGAAG[C/T]TTCCTCCATCTGCCT	55159
rs537494408	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656989	TTTCCTTTCCTTCTT[A/T]TTGGTTAGTTTATTG	55159
rs537506836	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664559	GGAGACCAGCCTGGG[C/G]AACACGGCAAAACCC	55159
rs537578187	in-del	-/T	0.00679313	0.0578828	intron-variant	RFWD3	GRCh38.p7	16:74643853	CTAATTTTTTTGTAT[-/T]TTTTTAGTAGAGACG	55159
rs537706157	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655571	GCTCTTTTACTGTTC[C/T]GAAAATCCTAGGGTG	55159
rs537777608	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74653968	GTTGCTTTTCTTTTT[A/T]GGAAATTGAGATATA	55159
rs537815278	in-del	-/A	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74634440	CCCATGCTAAGGTGC[-/A]GTGGCACCATCATGG	55159
rs537976869	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74626197	AAGCAATCTCACATA[A/C]ACACATATGCGGATA	55159
rs538070057	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624749	ACCTGTAATTCCAAC[A/C]CTTTGGGAGTCTGAG	55159
rs538074822	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625552	AGGCGCAATGGCTCA[C/T]GCCTATAATCCAACC	55159
rs538110824	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667956	GGGGAGTAAAGACTC[C/T]AGTAACCCTCAAGCA	55159
rs538179621	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624411	CACCCTTTTTTTTCT[G/T]TGAGACGGAGTCTCA	55159
rs538204781	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653402	AGGAGGATCACTTGA[C/G]CCCGAGAGTTTGAGG	55159
rs538284753	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647628	ATGAAGTCGTGCTCC[A/G]TCTCCCAAGCTAGAG	55159
rs538294361	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659196	TGTGCTTGACCAAGA[G/T]GAATCCACTCTGCGT	55159
rs538432928	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74647122	TTTATGTACTGATAA[A/C]AGAAAGCTCTCCAAG	55159
rs538497039	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74636964	GTGATCCACCCGCCT[C/T]GGCCGCCCAAAGTGC	55159
rs538520800	snp	C/T	0.00318978	0.0398085	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666841	AAGACTCGGTAGTTA[C/T]CTCGGCCGCACTCCG	55159
rs538547929	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668360	AAAGAAGAGTAGAAA[C/G]GGATATTCTTAAGGA	55159
rs538554948	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663148	TGACCTGGTGATCTG[C/T]CAGCCTCAGCCTCCC	55159
rs538559683	snp	C/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74647053	GATCATGCCACTGCA[C/T]TCCAGCCTGGGTGAC	55159
rs538566289	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631551	ATTTTTAAAACAATA[C/G]TTATAAAGGCACGGA	55159
rs538574386	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642519	TATCTTTATTTTTTT[A/G]AGACAGGTTCTTACT	55159
rs538602055	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74632261	GCCAGGCATGGTTGC[A/G]GGCGCCTGTAGTCCT	55159
rs538635670	snp	C/G/T	0.00065887	0.0181384	missense	RFWD3	GRCh38.p7	16:74652015	GAACTACTAGACACC[C/G/T]GCAACTCTTCAGATA	55159
rs538643030	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625441	ATTGCTTGAACCTGG[A/G]AGGTGGAGGTGGCAG	55159
rs538696475	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652819	TTTGAGCTGAGGAGT[C/T]TGAGGCCACTTTTGT	55159
rs538713604	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631871	GCTGATTGCCTGCCT[C/T]GGCCTCACAAAGCGC	55159
rs538718306	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663095	ATTTTTAGTACAGCC[A/G]GGGTTTCACTGTGTT	55159
rs538735504	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74624372	TCAATAAGATAAAGT[A/C]CCTGTCTTTGCCCTC	55159
rs538771500	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74628773	GCAGAGGAGGTTAAA[C/T]GCCTTTAGTCACTAT	55159
rs538795958	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653550	GAGTTTGGTGGCTTA[C/T]GCCTATAATCCCAGC	55159
rs538866691	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642359	AAACTCCTGAGCTCA[A/G]GCGATCTGCCTGCCT	55159
rs538929512	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648737	CTGAGATCGCACCAC[C/T]GCACTCCACCCTGGG	55159
rs539007451	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649076	GAGAGTGAGACCTAG[C/T]CTCTAAAAATAAATA	55159
rs539007994	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74633125	CTACTAAAACACAAA[A/G]AATTAGCCAGGCGTG	55159
rs539010070	snp	C/T	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74658471	CCCAGGCTTTCAACA[C/T]CTGGCCCAGGGACAG	55159
rs539036836	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74665098	AATGGCCACAACAGG[A/C]AGGACGAAAGCCCCT	55159
rs539200497	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662697	TCACTGATGAACAGG[A/C]CACCATTATTAAAGG	55159
rs539222612	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633882	TTGAGCCCAGGAGGC[A/G]GAGGTTGTAATGAGC	55159
rs539233394	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660224	TCTCTGAGCGGAGAT[C/T]GCACCACTGCGCTCC	55159
rs539356763	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667585	CGCGAGCCCACAGCC[A/G]TCTCGGCTCCGAGCC	55159
rs539405976	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74626611	CACAAAAAATTAACC[A/C]AGTACCCAAACCTCA	55159
rs539491797	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74630271	TGGCTAACATTTTTT[C/T]GTATTTTCAGTAGAG	55159
rs539569703	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74658148	CCTTCCCTGCACTTA[A/C]CAACTTTGAATTTTG	55159
rs539595379	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74640612	GGCGCCACTGCACTC[C/T]GGCCTTTGTGATAGA	55159
rs539620425	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74666034	ATAACAGGAAAAAGG[A/G]AGGAAGAGAGAGGGA	55159
rs539758016	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665481	TACTTGGGAGGCTGA[A/G]GCAGGAGAATCGCTT	55159
rs539902709	snp	G/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74654031	CAATTCAGTGTTGTT[G/T]TTTTTTAGCATAACC	55159
rs539952974	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648600	GTATGGTGAAACCCC[A/G]TCTCTAACTTAAAAG	55159
rs540088126	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648024	CAATCATGGCTCACT[A/G]AAGCCTTGACCTCCC	55159
rs540131218	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625147	GGAGGTTGTAGTAAG[C/G]CAAGATTGCACCTCT	55159
rs540172108	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74658938	ACGCCCGGCTAATTT[G/T]TTGTATTTTTAGTAG	55159
rs540189984	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74637104	AAGTCCTTAATGGTG[A/G]TTTCGTTTAAAGTCC	55159
rs540250680	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643384	TCATGCATACACCAC[C/T]GTTCATTCAACTAAG	55159
rs540277915	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668582	CATTCCTGTATGGAT[A/G]AAAATTTTGCTGTTT	55159
rs540331349	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74665868	TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA	55159
rs540343029	snp	C/T	3.13023e-05	0.00395603	intron-variant	RFWD3	GRCh38.p7	16:74636610	TTATAAATACAAAGC[C/T]TTTTAATTTGATATT	55159
rs540369990	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74650047	TGCAGCCCTGGGCAA[A/C]CACTAATATTATCTC	55159
rs540387458	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74625591	TCTGCCATTGACTTG[C/T]TGTGGAAGCCAGATC	55159
rs540396818	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643752	GCAATTTCGGCTCAC[C/T]GCAAGCTCTGCCTCA	55159
rs540406183	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640053	TATAAGAAAAAACAT[A/G]CTACGGTTTCAGGCA	55159
rs540421895	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74659464	GCCAAGCCTGCTGGT[A/G]CACGCCTGCAATCCC	55159
rs540435537	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660318	ATTAGTTAGGTGTGG[C/T]GGCACGCGCCTGTAA	55159
rs540496628	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641769	CTCTACTAAAAATAC[A/C]AAAAAAATTAGCTGG	55159
rs540577144	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634884	TGGTGGCTCATGCCT[A/G]TAATCCCAGTACTTT	55159
rs540663854	snp	A/T	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74635169	CCTGTAGTCCCAGCT[A/T]CTCAGGAGGCTGAGG	55159
rs540737189	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642247	CGTGCCTCAGCCTCC[C/T]GAGTTGCTGGCATTA	55159
rs540740409	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634239	TCTGTCTGAAATGAA[A/C]TGAAACAGATGACAT	55159
rs540758662	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635492	AAAAAAATCAACAAG[A/G]TAACAGAAATACACA	55159
rs540849624	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74647349	CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACC	55159
rs540889879	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658079	AAAACCAACAGGAAG[C/T]AGTGCTAGGGTTTCT	55159
rs540894926	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645099	AGAAAACACAATGGT[A/C]AATAAGTGTTTGCTT	55159
rs541016438	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666844	ACTCGGTAGTTACCT[C/G]GGCCGCACTCCGAAT	55159
rs541209222	snp	C/T	8.23689e-05	0.00641698	synonymous-codon	RFWD3	GRCh38.p7	16:74644559	GGGACATTTTCGTAC[C/T]TGTCCTTTAAGCCAC	55159
rs541217875	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638573	CACTCCAGTAAGATA[C/T]GCAAGAAAAAGATGA	55159
rs541247322	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639227	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	55159
rs541256222	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665232	CGGATGGATCACTTA[C/T]GCTCTGGTGTTCCAG	55159
rs541288554	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655865	CTACAAAGCCTGGAT[A/G]ACAGCTTATCTGTTT	55159
rs541379816	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639150	TTCAAGAGATTTCTT[C/G]CCTCAGCCTCCCAAG	55159
rs541384474	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621691	GGCATCAGGGTTTTT[G/T]TTTGTTTGTTTGTTT	55159
rs541395125	snp	A/G	0.00914312	0.0669923	intron-variant	RFWD3	GRCh38.p7	16:74624689	GGCGTGAGCCACCGC[A/G]TCTGGCCTCTAAAAA	55159
rs541529438	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660445	ACGACAGAGTGAGAC[A/G]CTGTCTCAAAAACAA	55159
rs541564675	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655762	CCATCTCCTGACCTC[C/G]TGATCTGCCCACCTC	55159
rs541589948	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74633097	GCCTGGCCAACACAG[C/T]GAAACCCTGTCTCTA	55159
rs541593076	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653270	CTTGAGCCTGGGAGA[C/T]TGAGGCTGCAGTGAG	55159
rs541616661	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74631087	CCCAAACTATCTGGA[G/T]TCCCTATTTTTTCTA	55159
rs541639178	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663367	AGGAAACATGGGAAT[A/G]TGGTGTCTTGGAAAA	55159
rs541830764	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620917	CGGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGATT	55159
rs541854578	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665611	GAAAAATAAAACAAT[A/G]AGCCGGGCGTGGTGG	55159
rs541869038	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627212	CAGAAGTGTGAGCAT[C/T]TAATGACTAACTCTG	55159
rs541915387	in-del	-/CTT			intron-variant	RFWD3	GRCh38.p7	16:74642446	TGAATCTATAATTAA[-/CTT]CTTCTTCTTTAAAAT	55159
rs542000689	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648800	AAAAAAAAGGGGATA[C/T]TCAGGTTGGGCATGG	55159
rs542039405	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643966	ACAGGCGTGAGCCAC[C/T]ATGCCCGGCCCTAGC	55159
rs542157274	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639485	AAGTAAAAGGCTAGG[C/T]AGGATCTTTATGAAG	55159
rs542240157	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659997	GAGGTCGAGGCTGCA[G/T]TGAGCTGTGATTGCA	55159
rs542331589	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667735	TGAATTGTGGTCCTA[C/T]TGTGGGAACAACCAG	55159
rs542337447	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630554	TGTTAGATGATTACT[A/G]TGAACCTGGCTATAC	55159
rs542341076	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665122	AGCCCCTCAATTAAA[C/G]GTTGAGAAGAGGTGG	55159
rs542394747	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662932	TTTTTTGAGATGGAG[C/T]CTCGCTCTGTTGCCC	55159
rs542399573	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637804	AACTAACATTAGCTT[A/C]CTCTTCCATTCCTAT	55159
rs542437502	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643372	ATTGTATTCTGTTCA[C/T]GCATACACCACCGTT	55159
rs542523458	in-del	-/C			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663850	TTCCCACTAAAGGGA[-/C]TGTAAAAACCAGGTA	55159
rs542560136	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642646	ACAGGTGTGTACCAC[C/T]ACACACGGATAATTT	55159
rs542594532	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629239	TGCTATGAAGTCGTT[C/T]GTGCCAAAGTTGCCA	55159
rs542685487	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645720	GAACTATTATGCAGC[C/G]CATGATCATAGTCAC	55159
rs542735356	snp	G/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74657090	ATTGCTCAGAGTCAA[G/T]AGTAGTCTTGCAAAT	55159
rs542800327	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635300	AAAAATAAAAAAAAT[A/T]AAAAATAAAAAAAAA	55159
rs542800416	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74640886	GGAGGTTGTAGTGAG[C/G]TGAGATCACGCCACT	55159
rs542817855	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667354	ATTTTGAATTTCGGA[A/G]CCTGTAAAGAGGCGT	55159
rs542850406	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630230	CCTTCTGAGTAGCTG[G/T]GATTACAGGCGTGTG	55159
rs542863137	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622979	TTCTCATGTTTTCAA[C/T]AGCAGTCTGAATAGC	55159
rs542875037	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641752	ACACGGTGAAACCCT[A/G]TCTCTACTAAAAATA	55159
rs542897118	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634806	TAAGACAGCCAGAGA[G/T]GAAAAAAAAAGGGGG	55159
rs542983745	snp	G/T	0.00199481	0.0315187	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666825	GCTCGCGAGCCCGCC[G/T]AAGACTCGGTAGTTA	55159
rs543026648	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630122	TTTTCTTGAGATGGC[A/G]TCTCACTCTGTTGCC	55159
rs543138390	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74635202	GAATGGCATGAACCC[A/G]AGAGGTGGAGCTTGC	55159
rs543170641	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622339	AAAGACGTCTTCAAA[C/T]AGGGGCCGGGTGCAG	55159
rs543281184	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666269	TCTTTTACTACATGG[G/T]GAAACTTTGGGCGGG	55159
rs543417027	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630441	TGACCAGATTTTACA[C/G]ATTAAGCTCACAGTG	55159
rs543431387	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656481	TTGAAATGATCCACC[A/G]TTCTTTTTTTTTCTT	55159
rs543494198	snp	G/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74649884	TGTCCTACACATCCT[G/T]GATTTGGCTGACTGC	55159
rs543527777	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661563	ATATCATTCTTAGCA[A/C]GACTGAGAAGCTTCA	55159
rs543570763	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667155	GTTTGGTTTTTTTTT[C/T]TTTTTTTAGCGCGTT	55159
rs543601185	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639906	ACAAATATCGAGATA[C/T]GTTGAGAGAGAGATG	55159
rs543646845	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74634911	CTTTCGGAGGCTGAG[A/C]TGGGTGAATCACCTG	55159
rs543690535	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74640344	AGAGACACGGTTTCA[C/T]CATGTTGGTCAGGCT	55159
rs543730019	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74633350	TGAAGAGAAGAAGAA[A/G]AAAAAAAAGAAAAAG	55159
rs543735065	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665772	TTTTTTTGAGATGGA[A/G]TTTCACTCTTGTTGC	55159
rs543760847	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645172	TCAGACTGGTATAAA[C/T]TGATGTCTGATGACA	55159
rs543913350	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656025	TTTCATGTCTGTTAA[C/T]ATAACATATTCTGCA	55159
rs543919802	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659229	CCCAACAAGAATGAG[G/T]GCATGGATAAGCAAG	55159
rs543930319	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622105	AGAAAGTCAAATCCT[A/C]AGCCTGCCCAGGCCC	55159
rs543941706	in-del	-/AC	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74632011	AGAAACAGGAAACAT[-/AC]AGTTTTGTAACCTTC	55159
rs543967352	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622926	TCTGAGGAATTGGCT[C/T]TATTTAGATAGGAAC	55159
rs543991251	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653088	TCATGTCTGTAATCC[C/T]AGCACTTTGGGAGGC	55159
rs544063970	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655477	TGGTCTCGATCTCCT[A/G]ACCTCGTGATTCGCC	55159
rs544084144	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637064	GTGAAATAAGGAGAG[C/G]ACAGAATCATAATAT	55159
rs544133753	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663387	GTCTTGGAAAAACAA[C/T]GTTTCAAGGAAGGAA	55159
rs544149107	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668263	ATTTCCTATTCTGCC[A/T]GTCACTGAATTCTCA	55159
rs544161943	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632317	GAATGGCCTGAACCC[A/G]GAAGGTGGAGCTTGC	55159
rs544197453	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645216	TGGGTAAATGAGATA[C/T]GGACATGCTTATATA	55159
rs544283280	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647232	GATGTTTTGACATTG[A/G]AAGAATTCACAGCAG	55159
rs544292997	in-del	-/GTTCCGCCTCCTGG	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74645834	CTCGGCTCACTGCAA[-/GTTCCGCCTCCTGG]GTTCACACCATTCTC	55159
rs544302312	in-del	-/A	0.249603	0.25	intron-variant	RFWD3	GRCh38.p7	16:74629666	ACCACTACCACCAAC[-/A]AAAAAAAAAAACCTT	55159
rs544321502	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646636	ACTAAAATACAAAAA[A/G]TTAGCCAGGCATGAC	55159
rs544324816	snp	G/T	4.94303e-05	0.00497119	missense	RFWD3	GRCh38.p7	16:74636519	CTCAGGACCCATGCT[G/T]GGGAGCCCCTGGGTT	55159
rs544394338	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624568	GCCCGGCTAATTTTC[C/T]TGTATTTTTGGTAGA	55159
rs544557842	in-del	-/AAG	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74653500	ATCTTCAAAAAAAAA[-/AAG]AAGAAGAAAAAATAA	55159
rs544568145	snp	A/C	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662980	CGCGATCTCGGCTCA[A/C]TGCAAGCTCCGCCTC	55159
rs544596771	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657581	CCCGGGTTCAAGCGA[C/T]TCTCCTGCCTCAGTC	55159
rs544716794	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663892	AATATTGAAAGATGG[C/T]GCTAAAAGAGAAGGG	55159
rs544730022	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74645290	TTTGGCATTATCCAT[G/T]AAAATTAAAACACAT	55159
rs544791210	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658195	TGTAGTCCTAGACTC[C/T]GTATGCTCCAGGAAA	55159
rs544833562	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652220	TATCACTTCAACCCA[C/T]CTCCAGGCCATTAAA	55159
rs544845958	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657155	AAGATAATTCTCTGG[A/G]AATGAGGCTTTGAAG	55159
rs544861544	snp	G/T			missense	RFWD3	GRCh38.p7	16:74626384	CAGTACACACCAGGA[G/T]GTTGCCATCATTCTC	55159
rs544928568	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667780	AATAGCTTTTGAAAC[G/T]GAGGGAGCAAGGAAC	55159
rs544967192	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658817	TTGTCACCCAGGCTG[G/T]ATTACAGTGACAAGA	55159
rs544994565	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665939	CTGGCCTCAGGTGAT[C/G]CGACTGCCTCGGCCT	55159
rs544998594	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74652371	TTAAAAGCTAATTCT[A/G]TTTTACTGGCATCTG	55159
rs545027989	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74653057	CACACAGACACATTA[C/G]GCTAGCTGCGATGAC	55159
rs545099394	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651389	TTGGGAGGCTGAGGT[A/G]GGTGGATCTCTTGAG	55159
rs545103869	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624552	AGACATCCACCACCA[A/C/T]GCCCGGCTAATTTTC	55159
rs545122217	snp	C/T	0.476052	0.106772	intron-variant	RFWD3	GRCh38.p7	16:74645745	AGTCACAAATATTTT[C/T]TTTTTTTTTTTTTTT	55159
rs545140006	snp	C/G/T	0.000576407	0.016967	missense	RFWD3	GRCh38.p7	16:74636393	GATATCACCAGGCAG[C/G/T]TCAGAGCATCACAGT	55159
rs545177574	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630597	TCTCCATCATATGAA[A/G]TAGCATGAATACAAA	55159
rs545273143	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74630026	TGGTTTAGCTTTGGA[A/T]TAGGGAAGTTTTAAA	55159
rs545301100	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643473	GGTACACAGCCTTCA[A/G]TGTTTCTTTAGAATG	55159
rs545392025	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662279	CACCTAGTTTTTAAA[A/G]TACATCAGTATAACT	55159
rs545527905	in-del	-/C	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74650683	TTTCTATTAAAAAAA[-/C]CTTCAAGCCTGGACA	55159
rs545615724	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668826	TTTGCCTCAATAAAC[A/G]TAGTATTCCATTGGA	55159
rs545627495	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648401	TTCAGGTGATCCACC[A/C]GCCTTGGCCTCCCAA	55159
rs545634278	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661662	ATAACCAGTTTTCCG[C/G]TTTGCCCTTAGAAAA	55159
rs545662991	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623050	ACTAGGGGAGACTCA[A/T]GTAAAAGCTTTGACC	55159
rs545697693	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656660	ACAAGGTTTCAACAT[A/G]TTGGCCAGGTTGGTC	55159
rs545720682	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74655203	ACAGGCTGACTCTCT[C/T]GTTAGGGGATAATGC	55159
rs545789121	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74628972	TGATGTGAAGCTTCT[A/G]GAAATGGGTTTAGCC	55159
rs545832843	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638615	GATAAAGCTGCCCTT[A/T]TTAATTTTTATGGCA	55159
rs545881278	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74638266	TGTAAAAGATTAAAC[G/T]GACATGTTAAAAGGC	55159
rs545888293	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632934	AGCCTCCCAAAGTGC[A/T]GGGATTACAGGCATG	55159
rs545977164	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74659358	GGTCCCCAAATTACA[-/C]CATAAGGTGCCTTCA	55159
rs546043610	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642270	TGGCATTACAGGCAC[A/G]CACCACCACATCCGG	55159
rs546074727	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665013	ACAAACGCTGTTTTT[C/T]ATGTGTGCTGTGAGC	55159
rs546095862	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659968	CTGAGGTAGGAAGAT[C/T]GCCTAAGCCTGGGGA	55159
rs546128074	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637143	AAAAAAAAAAAAAAA[A/C]AACAACTTAAAAGGA	55159
rs546152933	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632461	ATCATAACACCGATA[C/T]GAATTCCATGCTACT	55159
rs546189051	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668844	GTATTCCATTGGAAA[A/G]CAAACAAAAGATATA	55159
rs546212734	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664691	AGAGTGGAGGTTACA[G/T]TGAGCCGAGATCACG	55159
rs546342289	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74642018	TAATTTACAAATACA[C/T]ATATAGCTAATCAAA	55159
rs546390028	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653137	TGTGCCTAGGAGTTC[C/G]AGACCAGCCTGATTA	55159
rs546454441	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647019	GTGAACCTGGGAGGC[A/G]GAGCCTGCAGTGAGC	55159
rs546463770	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658403	GCTCACTACTTAGCT[C/T]TCCATAGCTTTGGCT	55159
rs546468692	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642588	TCACTGCAGCCACAA[A/C/T]CTCCTGGGCTCAAGA	55159
rs546539679	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631346	GTGTGGTGGCATGCA[A/C]CTGTAATCCCAGCTA	55159
rs546542225	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647386	TCCGCCTCTCAGATT[A/C]AAGTGACTCTCCTGC	55159
rs546566295	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74625130	ACTTGAACCCAGGAG[C/G]TGGAGGTTGTAGTAA	55159
rs546609407	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74637423	CCTGAAGTCAGGTGT[C/T]CAAGACTAGCCTGGC	55159
rs546634363	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624366	GAAGGGTCAATAAGA[G/T]AAAGTCCCTGTCTTT	55159
rs546646067	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632226	AAACCCCGTCTCTAC[C/T]ACAAAAATAGAAAAT	55159
rs546646350	snp	A/C/G	0.00114667	0.0239172	synonymous-codon	RFWD3	GRCh38.p7	16:74637934	TGCTGATTCTAACTC[A/C/G]GCCTGTTTCCTTAGC	55159
rs546656091	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74643761	GCTCACTGCAAGCTC[A/T]GCCTCACGGGTTCAC	55159
rs546675732	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642307	TTTTGTATTTTTAGT[A/G]AAGATGGGGTTTTGC	55159
rs546778218	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635568	ACTATCAAGCGGACT[A/G]GAATGGACACGTTAA	55159
rs546782022	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640666	ATTTTTTGGCCAGGC[A/G]CAGTGGCTCATGCCT	55159
rs546816907	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636063	TAAGTTGAGGACATA[C/T]AAGTCCTTCTTGGAC	55159
rs546871459	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663186	TCGGATTATAGGCAT[A/G]AGCCACCGCGCCCGG	55159
rs546872234	snp	C/G	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74627323	ATTTGAAACCCAGAT[C/G]TACCCTGTCAACTTT	55159
rs546917773	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636260	GTGATTTGGTAACCT[C/T]TGAGTCTTGAATTTT	55159
rs546943012	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645898	GCTGGGACTACAGGC[A/G]CCTGCCACCAAGCCC	55159
rs546962893	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663519	GTCAGAGGCCAGACT[A/G]GTGCAGGCTGAATAA	55159
rs546980238	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74655553	TGCCCAGCTGAAGCC[A/G]ATGCTCTTTTACTGT	55159
rs546981819	snp	C/T	0.00517822	0.0506191	intron-variant	RFWD3	GRCh38.p7	16:74640665	AATTTTTTGGCCAGG[C/T]GCAGTGGCTCATGCC	55159
rs547009689	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624663	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT	55159
rs547099065	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668309	ACACCAAAGAAACCA[C/T]TGACAAGAGCTGAAG	55159
rs547118801	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622479	AAAAAATTTAAAAAA[C/G]GAAAAAATTATGTCC	55159
rs547202689	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660916	TGATCACAGACTTAT[C/T]CATATATTTATTTAC	55159
rs547317078	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642209	CTTACAGTAACCTCC[A/G]CCTCCCAGGTTCAAG	55159
rs547376029	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643991	CCTAGCAACTGTTTT[C/G]TGCTTCCGAAATCCT	55159
rs547408453	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646774	ATGCCACGTAGCTAT[C/T]AATAAGAACAAGATG	55159
rs547432685	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666002	CGCTTTTCTCTTTAT[A/G]ACACCTTTTTCTCTT	55159
rs547541219	snp	A/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74666330	GTAAAACAGGGATAA[A/T]ACAAGTCTTTACTCC	55159
rs547738261	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74633762	CGAGACCAGCCTGGG[A/C]AATATGGTGAAACCC	55159
rs547791109	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625378	ATACACAAATTAGCC[A/G]GGTATGGTTGGTGTG	55159
rs547792364	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660120	TCGAAGCTTCCTCCA[C/T]CTGCCTATGTAGAAA	55159
rs547807594	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643776	TGCCTCACGGGTTCA[C/T]GCCATTCTCCTGTCT	55159
rs547885649	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74634130	CTGTTGAGAGACAGA[A/G]TATTTCACCAGAACC	55159
rs547889906	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665947	AGGTGATCCGACTGC[C/T]TCGGCCTCCCAAAGT	55159
rs547923976	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74654925	AAGCTGAGAAGTGAG[A/G]AAGCTGCAGGAAGTT	55159
rs547925373	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626003	CCAGCCTGGCCAACA[A/C]GGTGAAACCCTGTCT	55159
rs548013520	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638375	ATCTGAAGTTAAAAA[C/G]AGCAAAAGTAGACAT	55159
rs548097839	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664821	ACTGCTAGAAACACA[C/T]ATAGGGCGGGTGACT	55159
rs548121341	snp	C/G	0	0	intron-variant	RFWD3	GRCh38.p7	16:74626768	AAATTTAGAACCATA[C/G]GCTAGGAATCAAGTT	55159
rs548123185	snp	A/C/T	6.59326e-05	0.00574125	missense	RFWD3	GRCh38.p7	16:74632617	TCTGTTTGCCATGCA[A/C/T]CGGAATGTACTGACT	55159
rs548191767	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648527	CCTATAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	55159
rs548284378	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633225	GAGGTTGTAGTGAGA[A/C]AAGATTGCACCACTA	55159
rs548378112	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74625821	TTGGCACTAAGCACA[C/T]TTTAAGTGCTCATGT	55159
rs548587489	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668379	TATTCTTAAGGAAAT[A/G]TTCCCCTATGAAGCA	55159
rs548596973	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658844	AAGATCTTGGCTCAC[C/T]GCAAGCTCCGCCTCC	55159
rs548672741	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664766	AAAAGAAAAAAGAAA[G/T]AAATAAAATAAGTTC	55159
rs548675005	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74659015	TCCGCCTGCCTTGGC[C/T]GCTCAAAGTTCTGAG	55159
rs548717412	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632157	GCACTTCAGGAGGCC[A/G]AGGCGGGCGGATCAT	55159
rs548733330	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659670	GGCATCTGTCATCCT[C/T]GATGGGCACTACAGA	55159
rs548873645	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650865	CTGGGGGACAGAGTG[C/T]AACCCTGTCTCAAAA	55159
rs548914821	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661772	AAGTAATCTCTCAGA[C/G]ACTTTGCAGTTCTCT	55159
rs549034755	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662401	ACCTGTTATGCAGAC[A/T]AGACACCCTAGAGGC	55159
rs549036000	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627303	TTTTAGGGCTAGCAT[A/G]AATTATTTGAAACCC	55159
rs549038761	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623704	AACCCAAGAAATGGA[A/T]AATGTAGATAAAGTA	55159
rs549055026	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666980	TCTTCTTCTTCAATG[A/G]GTCCCCCGATAGCTG	55159
rs549074549	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656774	ATCCACCATCCTTGA[C/T]GCCCCTAAGAACATT	55159
rs549135947	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650380	TTTGGCAATGGGGGT[A/G]GGGGGCTGGTGTGTG	55159
rs549136047	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657215	CTGTTGGTTTTTACT[A/G]TGATTACAGGCAGAT	55159
rs549163160	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74656044	ACATATTCTGCAGCC[C/T]AACTTTCAAGACTTA	55159
rs549212476	snp	C/T	0.000314354	0.0125331	missense	RFWD3	GRCh38.p7	16:74644693	CTTCTTCCTCATCCA[C/T]AGAAGCAGAAGGTAG	55159
rs549238548	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660663	TGAAGAAAGAATTTT[C/T]GGTGTACAAGACACA	55159
rs549245583	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666550	ATCGCCCCGAGCTCT[C/T]GCCTGCCCAGCCCCC	55159
rs549302073	snp	A/G	0.00517822	0.0506191	intron-variant	RFWD3	GRCh38.p7	16:74655494	CCTCGTGATTCGCCC[A/G]CCTCGGCCTCCCAAA	55159
rs549452742	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622571	GCAACAACCCCTTGC[C/T]GGAGAGAAAGATCCT	55159
rs549508602	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630301	GACGGGGTTTTACCA[C/T]GTTGGTCAGGCTGGT	55159
rs549532003	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648881	CCTTGAGCCCAGGAG[C/T]TCGAAACCAACTGGG	55159
rs549587114	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74642435	GGCCCTTCTACTGAA[G/T]CTATAATTAACTTCT	55159
rs549667750	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634412	TATTTTGAGACAAGG[C/T]CTCACTCTGTCACCC	55159
rs549676524	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621757	GGAGTGCAGTGGCGC[A/G]ATCTCGACTCACTGC	55159
rs549739064	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631064	CTTACTGAGAACACA[C/G]TCATACTCCCAAACT	55159
rs549758408	snp	A/G	4.97739e-05	0.00498844	intron-variant	RFWD3	GRCh38.p7	16:74628673	AGTGGGCATCTGAAA[A/G]GAAAGTAAGGAAACT	55159
rs549873711	snp	A/C/T	3.32847e-05	0.00407939	missense	RFWD3	GRCh38.p7	16:74661361	AGGGCTGGTCCCCCT[A/C/T]GGCTGCTGGCCATGC	55159
rs549873767	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666888	CTGCCACTTCCGGAG[C/G]CGCTCAAGCTCCCGC	55159
rs549935120	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74661701	CCTGTGATCATAGTA[A/G]TATCTTCCAAAATAG	55159
rs550008414	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666453	CTGAGGAGCCCGAGG[A/C]TAGGCTCTCGGGGGA	55159
rs550028910	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665336	TCACACCTGTAATCC[C/G]AGCACTTTGGGAAGC	55159
rs550070443	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633884	GAGCCCAGGAGGCGG[A/G]GGTTGTAATGAGCTG	55159
rs550118138	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639305	AGCCTCCCAAAGTGC[C/T]GGGATTACAGGTGTG	55159
rs550193544	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74644079	GAGAACTGCTGTGGC[A/G]GGGGGTGGTCAGGGA	55159
rs550267461	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648616	TCTCTAACTTAAAAG[A/G]CAAAAATTAGCTGGG	55159
rs550271961	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74628171	AGAGCTGGCCCCCTT[C/G]TTCCACTACTGTTCT	55159
rs550343288	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655069	TAGCTAAGACAATTG[A/C]TGAAAGTATCTACAC	55159
rs550356082	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658249	CACCAATATATCTAG[A/G]GCAAAGTTTAGTCTC	55159
rs550371455	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646544	TGTAATCCTAGCACT[C/T]TGGGAGGCCAAGGCA	55159
rs550457773	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74631630	AACGCTGTGACTAAG[A/G]GTATAAAAGAAGTCA	55159
rs550530132	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652592	CTTCATCTCTCATTT[C/T]AGGATAGTATTTTTC	55159
rs550588651	snp	A/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74641870	GGCGGGAAGTTGTAG[A/T]GAGCCAAGATTGCAC	55159
rs550607672	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652709	GACCTGGGGCCAAAT[A/C]TAACACTCCAAATAT	55159
rs550623933	snp	A/C	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74636864	TACATGCACCCACTA[A/C]CATGCCCGGCTAATT	55159
rs550625973	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642290	ACCACATCCGGATAA[A/T]TTTTTGTATTTTTAG	55159
rs550816183	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635470	AGACTCCATCTCAAA[A/G]GAAAAAAAAAAAATC	55159
rs550838775	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667504	CAAATCACTTGTTAG[G/T]GCCGCCGCTCGCCGC	55159
rs550867779	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645370	TATATAGTCATGCAT[C/T]GCTTGACAATGGGAA	55159
rs550911478	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636012	TAACCCTTAGGGCTG[C/T]GTTTTGTCAAACATT	55159
rs550952554	snp	A/C			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621030	CACGCCTGTAATCCC[A/C]GCACTTTGGGAGGCT	55159
rs550999288	snp	A/C	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74630610	AAATAGCATGAATAC[A/C]AACTCTTATTAATAA	55159
rs551041872	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623774	ATCTGTAGTGTCTCA[A/G]TGACCTAGGGTCCTA	55159
rs551230150	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667479	AGGGATCTGAGCTAC[C/T]GAACAGTCTCAAATC	55159
rs551274636	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650926	ACCCACTTCATCAAC[C/T]ATCTGATTGTCCAAA	55159
rs551366770	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667014	CAGCGGTGCTCTCAT[G/T]GGCTGGTAGTTCGTC	55159
rs551398500	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622538	CAACTAGAACTTGGA[A/G]CTCTGGGGAAATCTA	55159
rs551409098	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657710	AACTCGTGACCTCAG[A/G]TGATTCGCCTGCCTC	55159
rs551432585	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646839	GCACTTTGGGAGCCC[A/G]AAGCGGGCGGATCAC	55159
rs551449213	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651115	TATATTTCAATTCAT[A/C]ATCCAAGAATATTCT	55159
rs551487447	snp	C/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74647579	AGGTGTGAGCCACTG[C/T]GCCCGGCCAACATTA	55159
rs551516247	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74651866	TCTAGCCTTCCGAAA[G/T]TTAAGCTTCATGGAT	55159
rs551563365	in-del	-/AT	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74633420	ACCTACTGTATAAAC[-/AT]GTGATGGAATACCAC	55159
rs551636288	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623302	CCCAGCACTTCACAC[C/G]TGGAACACAAGTGTT	55159
rs551642954	snp	A/G	5.72142e-05	0.00534826	intron-variant	RFWD3	GRCh38.p7	16:74624095	CACAAGCAGAGGGAA[A/G]GGTCAGGAGTCAGTC	55159
rs551647181	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74633439	GATGGAATACCACCC[A/G]TTAAAAAGGAATTAA	55159
rs551658420	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627720	ACATCTGGTCATGGG[C/T]CAGGCAGGCATTAGG	55159
rs551671571	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649382	TTTATTTTTAAAAAT[G/T]TAGTTTGAATATTCT	55159
rs551685515	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630246	GATTACAGGCGTGTG[C/T]CACCACGCATGGCTA	55159
rs551713526	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640480	AGTAGCAATGAAAAT[C/T]TGTACAGAAAAATAT	55159
rs551740487	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656099	CAGTGGCTCACACCT[A/G]TAATCTCAGTACTTT	55159
rs551763949	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664896	AAAGTTCTATGGAAC[A/G]GTGCAGTTCTGGAGC	55159
rs551847297	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74629531	AGGTGTGGTGGCACA[C/T]GCGTATAGTCCCAGC	55159
rs551855980	snp	A/C/G			intron-variant	RFWD3	GRCh38.p7	16:74651580	GCTGAGATTGTTGTC[A/C/G]CTGCACTCCAGTTGT	55159
rs551869359	in-del	-/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74630264	CACGCATGGCTAACA[-/T]TTTTTTTGTATTTTC	55159
rs551888730	in-del	-/AC	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74638657	ACCCCCAAAACAATT[-/AC]AGTTTAGCAACGCTG	55159
rs551935926	snp	A/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74633209	TTGAACCCAGGAGGC[A/G]GAGGTTGTAGTGAGA	55159
rs551941320	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74649469	CAATTTAAAAAATAA[C/T]CAATATTTTGCCAAT	55159
rs551948554	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632065	ATATTTTAAATGGAT[C/T]TCAGAAGACACAGTC	55159
rs551949491	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647870	GTGCTGGGATTATAG[C/G]CATGGGCCACCGCGC	55159
rs552016142	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74625650	GACTTGTGTATATGC[A/T]TTCTGTGCTATCATT	55159
rs552061885	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647615	ACTATTCTTTGAGAT[A/G]AAGTCGTGCTCCGTC	55159
rs552105321	snp	C/T			missense	RFWD3	GRCh38.p7	16:74644558	GGGGACATTTTCGTA[C/T]TTGTCCTTTAAGCCA	55159
rs552105458	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74666212	GATAGATAGATAGAT[A/T]GATAGATAGATTGAT	55159
rs552108764	snp	C/G/T	8.65185e-05	0.00657668	intron-variant	RFWD3	GRCh38.p7	16:74632689	CTGAAAAAGGCAAAA[C/G/T]AGTATGAAATAGATC	55159
rs552239006	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74632111	CAGAGCTAAGGTCGG[A/C]TGGGCGCAGTGGCTC	55159
rs552401883	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74653283	GATTGAGGCTGCAGT[A/G]AGCCATGATGGTGCC	55159
rs552402774	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631483	CTCTCTCTCTCAAAA[A/G]TAAATAAATAATAAC	55159
rs552688056	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668392	ATGTTCCCCTATGAA[C/G]CAACTACACCAACAA	55159
rs552735719	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664184	TTCAACTCCTCGGCT[A/C]AAGCAACCCTTCTGC	55159
rs552944581	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667952	AACAGGGGAGTAAAG[A/T]CTCCAGTAACCCTCA	55159
rs552961318	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624898	TCAAGAGGCTGAAGG[A/C]GGATTGCTTAAGCTG	55159
rs552993633	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74631753	AACCTGGTATGGCGA[C/T]TCTGATGTCAGGCAC	55159
rs553076122	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657514	GGAGTCTCGCTCTGC[A/G]GCCCAGGCTGGAGTG	55159
rs553105949	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636943	GTCTTGAACTCCTGA[A/C]CTCAGGTGATCCACC	55159
rs553176512	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74630319	TGGTCAGGCTGGTCT[C/T]GAATTCCTGACCTCC	55159
rs553182267	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639100	CTGCAGAGCAGTGGC[A/G]TGATCCAGGCTCACG	55159
rs553194359	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74643135	TGACTACCTATAGAG[A/C]TTTTTTTCTTTCTTT	55159
rs553214984	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640209	GTGCAGTGGCGTGAT[A/C]TTGGCTCACTGCAAC	55159
rs553215256	snp	C/G	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74634818	AGAGGAAAAAAAAAG[C/G]GGGGAAGGGGGGCGC	55159
rs553228394	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646486	AACCATGCTTTACAT[A/G]ATAAGAAAAAGAATT	55159
rs553254108	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635148	AGCTGGGTGTGGTGG[A/C]GGGCGCCTGTAGTCC	55159
rs553268226	in-del	-/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74659345	TTTACTTTGGGAGGG[-/T]CCCCAAATTACACCA	55159
rs553270139	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637520	TAATCCCAGCACCTC[A/G]AGATGCTGAGGCTGA	55159
rs553291272	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662157	AAAAAAAATTTTTTT[G/T]TGTTATATAGATGAA	55159
rs553319993	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623394	TAAAAGATTGTCAGC[C/T]TTCAAGGTCAGAAAT	55159
rs553335953	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648707	AACACGGGAGGCAGA[C/G]GTTATTGTGGTGAGC	55159
rs553428673	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667106	ACCTTGCACCCGCCC[C/G]GGAAAAAATGGGAGG	55159
rs553449862	snp	G/T	1.66593e-05	0.00288607	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623897	AACAACATCTAACCA[G/T]CAGCATGCCTTCAAG	55159
rs553509447	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626213	ACACATATGCGGATA[C/T]GTGGGATTACAGAGC	55159
rs553533644	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667557	CCGGAATTCTCCAGC[G/T]ACGTACGAGGAGCGC	55159
rs553644575	snp	A/C			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663656	ACATTTTTTTAAGAA[A/C]GGATAAATTAACCAG	55159
rs553689584	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665433	AAATACAAAAACTAC[A/C]CGGGTGTGGTGGCGC	55159
rs553786054	snp	A/C	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74632426	AAACAACAACAACAA[A/C]AAAAAACAGAGCTAA	55159
rs553793125	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662582	TTTAAAGAGTGAAAA[C/T]TGGGCTGAGGCATGA	55159
rs553879559	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74642942	TATACTAATTCCTTA[C/T]TGTAATCAGTGAATT	55159
rs553913267	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638104	TAGTGAATAAAATAT[A/G]AAAAGAGAAAAATCT	55159
rs553925839	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643019	CTTTTCAACAAAATT[C/T]CTCTCTGTACACATC	55159
rs554078516	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74664982	GGCTGGGCACCCCAA[A/T]CCTTGAGGATGTCAC	55159
rs554137313	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637707	TTTTGAACAGATGCC[A/C]TAATCAGAAATAAAA	55159
rs554195848	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659060	CCACTATGCCCAGCC[A/T]CATCAAGCAATTTTC	55159
rs554201629	in-del	-/T	0.0166325	0.0896639	intron-variant	RFWD3	GRCh38.p7	16:74666194	GATTAGATAGATAGA[-/T]TAGATAGATAGATAG	55159
rs554230936	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659268	CTTGCAAGAGGCCTC[C/G]TGACAGTCAGCCAGC	55159
rs554294211	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659778	AGAAGGCACAATTCC[A/C]ATTCCAGCCTTATCA	55159
rs554337501	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632379	CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA	55159
rs554353160	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74664937	TAACCACTGTAGGCC[A/G]GTCGGAGGTGCCTAG	55159
rs554374369	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74630771	AGGAAAAGAGTGAGT[A/G]GCTCCCTACCTGGCT	55159
rs554391626	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74647354	GTGCAATGGCACAAT[C/G]TCGGCTCACCACAAC	55159
rs554397453	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653604	GATTGCTTGAGGCCA[C/G]AAGTTTGAGACCAGA	55159
rs554410756	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642414	CAGGTGTGAGCCACT[A/G]TGCCTGGCCCTTCTA	55159
rs554447826	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74637592	GAGCCGAGATCACAT[C/G]ACTGCACTCCAGCCT	55159
rs554498203	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632795	CCTTGGGAACCAGCT[A/G]GTCAAACAAAAATTC	55159
rs554519415	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642233	GTTCAAGCGATTCTC[A/G]TGCCTCAGCCTCCCG	55159
rs554532722	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653008	CCTTATACTAAAAAC[C/G]AGGAGTTCCTGAGGA	55159
rs554742567	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632366	CAGTGCACTCCAGCC[G/T]GGGTGACAGAGCGAG	55159
rs554771429	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664564	CCAGCCTGGGCAACA[C/T]GGCAAAACCCCGTCT	55159
rs554818494	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624752	TGTAATTCCAACACT[C/T]TGGGAGTCTGAGATG	55159
rs554858414	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74624466	AGTGGCACGATCTTG[A/G]CTTACTGCAACATCT	55159
rs554874121	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652233	CATCTCCAGGCCATT[A/G]AATGCTGCCTTTGAA	55159
rs554919694	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639555	AATGGAAGGATATTA[C/T]ATAATGTTCATGACT	55159
rs555085125	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74647192	AACACAAAGAGCACA[C/T]AGAAATATGCAAAAA	55159
rs555122319	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634876	GCCAGGCATGGTGGC[C/T]CATGCCTGTAATCCC	55159
rs555209134	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645050	ATGTGTACCAGAGGG[C/T]AAAAAAAGAAAACAA	55159
rs555289669	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663281	AGAGGGCTGAAGACT[A/G]AAGTCAGAGACACTA	55159
rs555303666	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639868	TTTCCATGGTTTCTG[A/G]TATCTGTGATCAACC	55159
rs555319784	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645501	CAAACCTGTATAGGA[G/T]GTTACTGTACCAAAT	55159
rs555349299	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657931	TTAGGGTGTTGACAC[A/G]TATATCAATAGAATT	55159
rs555389605	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659499	ACTTAGGAGGCTGAG[A/G]CACAAGAATCGCTTG	55159
rs555489257	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622627	CAGAAGTGTTTTATA[A/G]TAAAAACGATAACAA	55159
rs555508978	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628004	TTCCAGAGGCAGAGA[C/T]GTTCAGCTGGCTGGG	55159
rs555525865	snp	A/T	0.000358781	0.0133889	intron-variant	RFWD3	GRCh38.p7	16:74649113	TAAATAGATTTTTTT[A/T]AAATGATGTTCATAT	55159
rs555537348	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623409	CTTCAAGGTCAGAAA[C/T]AAACCGGACACAAGG	55159
rs555569910	in-del	-/CTT	0.0271762	0.113356	intron-variant, cds-indel	RFWD3	GRCh38.p7	16:74662904	TTCAGAATGGTCATG[-/CTT]CTTTTTTTTTTTTTT	55159
rs555612908	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655086	GAAAGTATCTACACT[A/G]AAAAGATTCTCAGTG	55159
rs555625788	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631886	CGGCCTCACAAAGCG[C/T]TAGGATTACAGGCGT	55159
rs555631909	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661557	TGTTTAATATCATTC[C/T]TAGCAAGACTGAGAA	55159
rs555658508	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643850	CCGGCTAATTTTTTT[C/G]TATTTTTTAGTAGAG	55159
rs555665345	snp	C/T	0.000399281	0.0141238	splice-donor-variant	RFWD3	GRCh38.p7	16:74660931	CCATATATTTATTTA[C/T]CTGGCACTGTCTGTC	55159
rs555679626	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636080	AGTCCTTCTTGGACT[A/G]TATCAGTAACCTACA	55159
rs555898146	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639062	TTTTTTTTTTTAGCC[C/T]GAGTCTCACTCCATT	55159
rs555901449	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627963	GTGAATGAAGCACAG[G/T]CTGCTGTTATGCGTT	55159
rs555955681	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655725	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	55159
rs555978470	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648161	ATTTTTTCAACTGAT[A/C]CTTAACCTTGTTGGC	55159
rs555989390	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74665482	ACTTGGGAGGCTGAG[A/G]CAGGAGAATCGCTTG	55159
rs556047664	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645561	TTTCACCATGTTGGC[C/T]GGGCTGGTCCCGAAC	55159
rs556062270	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627173	ACAAAACTTAAAAAC[A/T]TGAGTAGACCCACCC	55159
rs556063108	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643319	ATGCAATCATACTAA[C/T]AACATGCTTCCACAG	55159
rs556154766	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74665140	TGAGAAGAGGTGGGC[A/G]GGGGAAGTGTTCAAA	55159
rs556158961	snp	C/G	3.29935e-05	0.00406149	synonymous-codon	RFWD3	GRCh38.p7	16:74628588	TGAAGCATCCTCCAA[C/G]GTTCCAGCCAGCACC	55159
rs556191013	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623603	TCCTAGATGATGAGA[C/G]GACACTCTCTAAGGT	55159
rs556249264	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74646962	GTGTGGTGGCAGGCG[C/G]CTGTAGTCCCAGCTA	55159
rs556331379	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655223	GGGGATAATGCTGCT[A/G]GTGACTTCAGTTGAA	55159
rs556399677	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660849	TTGCCAAAAGTCACA[C/T]TGTCAGTCCTTGAAT	55159
rs556408927	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663995	CAAAGCCCTTCTCCC[C/G/T]CTATGCACGAGAAAA	55159
rs556517315	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74632945	GTGCTGGGATTACAG[A/G]CATGAGCCACCACAC	55159
rs556542707	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74666047	GGGAGGAAGAGAGAG[A/G]GAGAGGGAGAGGCGG	55159
rs556544631	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74660235	AGATCGCACCACTGC[A/G]CTCCAGCCTGGGCGA	55159
rs556610745	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74654326	TATTTATATGCTAAC[C/T]TTTATTATTTCTTTC	55159
rs556627447	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74638197	AATGGGGACTAAAAA[C/T]GCCACAGGCAAAACG	55159
rs556679396	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668763	AGTAACTGTGTTGAA[A/G]AACATTCGTGTACGC	55159
rs556701985	snp	A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74643821	GCTGGGATTACAGGC[A/G]TCCGCCACTATGCCC	55159
rs556786158	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74635768	TTATGCTAAAGACAG[C/G]AGAAAGAAACATCTG	55159
rs556809093	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657430	GGAGATAATTCTCTG[C/T]GGTCCTTACTCTGCC	55159
rs556946424	snp	C/T	1.65765e-05	0.00287888	missense, intron-variant	RFWD3	GRCh38.p7	16:74630947	TCTGGACCACGGTAT[C/T]TGTCTCCAGGCTGTG	55159
rs556947581	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650745	AGCCAGGTGTGGAGG[C/T]ATGCACATGTAGTCC	55159
rs556987312	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636217	GCACCCTGGGGTACT[C/T]GCATTAACAAGGAAC	55159
rs557021698	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661581	CTGAGAAGCTTCAAG[A/T]GAAGATTTTAACTAC	55159
rs557035215	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74637835	TCCAAAAGTTCTTTG[C/G]ATTAGAAAGGACAAA	55159
rs557059192	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640831	GTAGTCTCAGCTACT[C/G]GTAAGGCTGAGGCAG	55159
rs557078652	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662063	CAAATATTTATTAAG[A/C]ACCTATGTTCTTTTC	55159
rs557098025	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641295	AGTCTCCCGAGTAGC[G/T]GGGACTACAGGTGCG	55159
rs557098688	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646081	AGATAATTATATAAG[A/T]TTGTTCCAAGCAGGC	55159
rs557197572	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639129	CGGCTACCTCCGCCC[A/C]CCGGGTTCAAGAGAT	55159
rs557201350	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644977	TACTTTTTCCTTCAC[G/T]CAAAGGAAGAAAAGC	55159
rs557238069	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74639441	AATCTGTCATTGACC[C/T]AAAGGTCATTATGCA	55159
rs557256170	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74651205	GCAGGACATCTACTT[C/T]AGGGGTCTCTGCCTA	55159
rs557264066	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74634662	CCAAAGTGCTGGGAT[G/T]ACAGTCATGAGCCAC	55159
rs557300599	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74629021	AAGAAACAAAGCTTA[C/T]ATACATAACAAAATA	55159
rs557333045	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645644	AAGTGTGAGCCACTG[C/T]GCCCAGCCTGGTATT	55159
rs557346477	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642632	GAGTAGCTGAGACTA[A/C/T]AGGTGTGTACCACTA	55159
rs557353076	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623360	TATCACACACTTGTG[G/T]GGAGATGAGACAAGT	55159
rs557363097	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630120	TTTTTTCTTGAGATG[A/G]CGTCTCACTCTGTTG	55159
rs557374465	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657026	CCACTGAATATCCAT[C/T]ACCTCAGGCAGGCCC	55159
rs557519777	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74637163	ACTTAAAAGGAGACA[G/T]GGTCTCACTCTGTCA	55159
rs557560432	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635107	AACACGGTGAAACTC[C/T]GTCTCTTCTAAAAAT	55159
rs557725054	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621755	CTGGAGTGCAGTGGC[A/G]CGATCTCGACTCACT	55159
rs557762214	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74641259	CCTCTGCCCCCTGGG[G/T]TCAAGCTATCCTCCT	55159
rs557766337	snp	A/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74635679	GATAAATCTTTTTAT[A/T]AAAAACTTAGATGGG	55159
rs557808543	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74666229	ATAGATAGATTGATT[A/G]GATACATAGATATTA	55159
rs557814156	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663565	ATAAACATAGTGGAC[C/G]AAGTACATATATGTA	55159
rs557849674	snp	C/G	0.0107246	0.0724382	intron-variant	RFWD3	GRCh38.p7	16:74658207	CTCCGTATGCTCCAG[C/G]AAAACAATATTGTGA	55159
rs557857123	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645615	GCCTTGGTCTCCCAA[A/C]GTGCTGGGATTATAA	55159
rs557872030	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666677	CCAAGCCCGCGTGCA[A/G]CCCACCTCGTGGGGT	55159
rs557967581	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645144	GCAAATTAAAGAGAC[C/T]ATTTTTCATCTATCA	55159
rs558001405	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648943	AAAAATGTAGCCGAG[G/T]GTGGTGGCATTACCT	55159
rs558067327	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74639114	CGTGATCCAGGCTCA[C/T]GGCTACCTCCGCCCC	55159
rs558088299	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622082	TCAATCAGCATCAGG[C/T]ACTTCAAAGAAAGTC	55159
rs558113243	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649811	ATTACAATTCCCCCT[C/T]ACCCATTTTTTTCCC	55159
rs558128279	in-del	-/TC	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74665747	AGACTTTTCTTTCTT[-/TC]TTTCTTTCTTTTTTT	55159
rs558141705	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628846	CAAAAGGACATACAT[A/G]TAATATTCTGCAACT	55159
rs558155607	in-del	-/AG	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74655263	CTTTTTTTTTGAGAC[-/AG]AGTCTCACTTTGTCG	55159
rs558213935	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663906	GCGCTAAAAGAGAAG[G/T]GCTGGTTAAAAGCCA	55159
rs558272217	snp	A/C/G	3.29469e-05	0.00405864	missense	RFWD3	GRCh38.p7	16:74661003	CCTCCTTCTTGTTCT[A/C/G]ATTGGCCCTACACTG	55159
rs558303118	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628125	GGCAGGCAGAAGATA[C/T]GAAAGTGATCTCAAG	55159
rs558307513	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74634626	ACTCCTGGGCCCAAA[C/T]GATCCTCCCGCCTTG	55159
rs558356837	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74647295	TAGGTGTTATTTTTA[-/T]TTTTTTTTTTGACAT	55159
rs558389456	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74632265	GGCATGGTTGCAGGC[A/G]CCTGTAGTCCTAGCT	55159
rs558400454	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647068	CTCCAGCCTGGGTGA[A/C]AGAGCGACACTCGTC	55159
rs558435574	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74642160	CAGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT	55159
rs558461282	snp	C/T	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74628779	GAGGTTAAACGCCTT[C/T]AGTCACTATCCTCTG	55159
rs558541446	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641631	CATTTGCATACAGTA[A/T]AAAAACTTTCTGGCC	55159
rs558549871	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74625478	GAGATTGCGCCTCTG[C/T]ACTCCAGCCTGGGTA	55159
rs558672808	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652823	AGCTGAGGAGTTTGA[C/G]GCCACTTTTGTCACA	55159
rs558687934	snp	A/G	4.95528e-05	0.00497734	missense, intron-variant	RFWD3	GRCh38.p7	16:74630820	TGCACATGACTGCTC[A/G]TGTTTCGCACGTCAT	55159
rs558840651	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74648780	ACTCCGTCTCAAAAA[A/C]AAAGAAAAAAAAGGG	55159
rs558890731	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657569	CAACATCCACCTCCC[A/G]GGTTCAAGCGATTCT	55159
rs558980167	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647108	AAAAAAGATTCAATT[C/T]TATGTACTGATAACA	55159
rs559020970	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74633187	GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCA	55159
rs559028712	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662775	TAGGGGTGCAAGAGC[A/G]TAAGCTAGGTGACCA	55159
rs559200307	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663119	CTGTGTTAGCCAGGA[C/T]GGTCTCGATCCCCTG	55159
rs559278170	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667617	GCCGCCGGCAGGAAA[A/G]CCACAAAGAAAACTG	55159
rs559302819	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662433	AAAACAGATAAGACC[C/T]CATGTATCAGAGTTT	55159
rs559317114	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623707	CCAAGAAATGGATAA[C/T]GTAGATAAAGTACCC	55159
rs559379362	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662941	ATGGAGTCTCGCTCT[A/G]TTGCCCAGGCTGGAG	55159
rs559386440	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650039	TTTGCATCTGCAGCC[C/G]TGGGCAACCACTAAT	55159
rs559395066	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651852	GCACAAATCTAGTTT[A/C]TAGCCTTCCGAAATT	55159
rs559472528	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639982	TCTATTTTATTATTT[A/T]TTATTGTTAATCTCT	55159
rs559518199	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667754	GGGAACAACCAGGAA[A/G]CTGTATGAGAAATAG	55159
rs559523218	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656558	CATGATATTGGCTCA[C/T]TGGAACCTTTCACCC	55159
rs559532183	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657675	GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	55159
rs559585164	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635856	AAAACCTAAAATTAA[A/G]CTTAAAAACACAAAA	55159
rs559585402	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630232	TTCTGAGTAGCTGGG[A/T]TTACAGGCGTGTGCC	55159
rs559622157	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630557	TAGATGATTACTATG[A/C]ACCTGGCTATACTTG	55159
rs559639432	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645248	TGTTGCCTTAAATGT[A/G]AAGTGGCACACATTT	55159
rs559659094	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656060	AACTTTCAAGACTTA[G/T]TATTTAAGAAATAAG	55159
rs559731172	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74637570	CCCAGGAGACAGAGG[C/T]TGCAGTGAGCCGAGA	55159
rs559761667	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74628356	TTAGCCTGTGAGCGG[C/T]ACCACAGCCACCCAA	55159
rs559774357	snp	C/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74647838	CTCAGGTGATCCGCC[C/G]GCCTTGGCCTCCAAC	55159
rs559799873	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622400	GAGGCTGAGGTGGGA[A/G]GATTGCTTGAGGCCA	55159
rs559861735	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648306	ACAAAGCCTGCAAGC[C/T]TCCCATTTTAACCTG	55159
rs559887949	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623015	TAAATTCTCTTATGT[A/C]TTTTCTCCTGATCTC	55159
rs559920828	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654080	AATCATAACCATTAT[C/T]TGGTTCCAAAACATT	55159
rs559997317	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629257	GCCAAAGTTGCCAAA[C/G]TGTCTACTTTGCCTG	55159
rs560033390	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661647	CTATAACAAGCATTT[A/T]TAACCAGTTTTCCGG	55159
rs560036153	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625607	TGTGGAAGCCAGATC[A/C]GCTGTCTTATAGAAC	55159
rs560074796	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627155	GGATGTTTCTCAGCT[C/T]AAACAAAACTTAAAA	55159
rs560113274	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632082	CAGAAGACACAGTCT[A/C]AGACCAAAAAAAACA	55159
rs560158152	snp	A/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74646128	ACCTACAGTCCCAGC[A/T]TATTGGGAGGCCAAG	55159
rs560160004	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74625157	GTAAGCCAAGATTGC[A/G]CCTCTGCACTCCAGC	55159
rs560169198	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664671	GGAGAACCCCTTGAA[C/T]CCGGAGAGTGGAGGT	55159
rs560225098	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637139	AAAAAAAAAAAAAAA[A/C]AAAAAACAACTTAAA	55159
rs560225232	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631424	GTTGCAGTGAGCTAA[A/G]ATCATGCCACTGTAC	55159
rs560306953	snp	A/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74666475	CTCGGGGGAAGGGCC[A/G]GGCGACCTCCCACCC	55159
rs560356347	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642248	GTGCCTCAGCCTCCC[A/G]AGTTGCTGGCATTAC	55159
rs560375571	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658939	CGCCCGGCTAATTTT[C/T]TGTATTTTTAGTAGA	55159
rs560559292	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668331	GAGCTGAAGTGGGAG[A/G]AAAAAAACACAGGAA	55159
rs560568255	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625153	TGTAGTAAGCCAAGA[C/T]TGCACCTCTGCACTC	55159
rs560722774	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641787	AAAAATTAGCTGGGC[A/G]TGGTGAAAGGCGCCT	55159
rs560733396	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652348	CACAAAGGAGCTTGA[C/T]CCTTCCGTTAAAAGC	55159
rs560734227	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647820	TGGTCTTGAACTCCT[A/G]ACCTCAGGTGATCCG	55159
rs560827078	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663406	TCAAGGAAGGAACAA[C/T]TGAGTGTCAAGTGCT	55159
rs560881226	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642294	CATCCGGATAATTTT[C/T]TGTATTTTTAGTAAA	55159
rs560886543	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74658301	ATATTTGATGAATGA[C/G]TGATGACCCCCACTG	55159
rs560888352	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664046	GGCTTACACTCAGGA[C/T]GGAGAGTGGCACAGT	55159
rs560919433	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625110	GAGGCTGAAGCACAA[A/G]AATCACTTGAACCCA	55159
rs560997340	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641135	TGGAGACAACCTAAA[A/T]GTCTACCAATGTAAA	55159
rs561002074	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653090	ATGTCTGTAATCCTA[A/G]CACTTTGGGAGGCCA	55159
rs561200881	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631294	TTTGAGACCAGCCTG[A/G]CCAACATGGCGAAAC	55159
rs561241424	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624617	GGCCAGGCTGGTCTA[C/G]AACTCCTGACCTCAG	55159
rs561345086	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634217	TTGTCAGTCAAGATA[A/T]GTCACATCTGTCTGA	55159
rs561368160	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74653388	TGGGAGGCTGAGGCA[G/T]GAGGATCACTTGAGC	55159
rs561418858	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638758	TAAAAAATTCATTCA[A/C]AACAATTTTAACAGC	55159
rs561425611	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74633276	GAGCAAAACTCCGTC[G/T]CAGAAAAAAAAAAAA	55159
rs561456198	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633797	GCTACAAAAAATATG[A/C]GAATTAGCTGGGCGT	55159
rs561543394	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666276	CTACATGGGGAAACT[C/T]TGGGCGGGTTTCCTA	55159
rs561555617	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74627702	AAGTTTCCTGTGAGA[A/G]GGACATCTGGTCATG	55159
rs561576010	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637593	AGCCGAGATCACATC[A/G]CTGCACTCCAGCCTA	55159
rs561590351	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632902	CAACTTCTGCCTCCC[A/G]GTGATCTGCTCGCCT	55159
rs561614663	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74657834	TCTTGAGATTCTAAG[G/T]GAACAGCAGCTATAG	55159
rs561673476	snp	C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74651606	GTTGTCACTGGGGGA[C/T]AGAGCCAGACCTTGC	55159
rs561796027	snp	A/C/G	8.23676e-05	0.00641693	intron-variant	RFWD3	GRCh38.p7	16:74644480	AATAGGACATAATTA[A/C/G]AGTGGTTCTAGGAAT	55159
rs561809974	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635942	TTCTCTTATTTGGAA[A/G]TTGTTAACTTGAACA	55159
rs561851715	in-del	-/C	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74659600	CTCTTGTCTTAAAAA[-/C]CAAAAAAAAAACCCA	55159
rs561882489	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648816	TCAGGTTGGGCATGG[G/T]GGCTCATGACTACAA	55159
rs561883735	in-del	-/C/CCGCCGAAGACTCGGTAGTTACCG	0.00716266	0.059414	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666843	ACTCGGTAGTTACCT[-/C/CCGCCGAAGACTCGGTAGTTACCG]CGGCCGCACTCCGAA	55159
rs561893175	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655805	TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC	55159
rs561907513	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662247	GACAACAGGACTGAG[C/T]CACTGTGCCTCCCTA	55159
rs561928617	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74655264	TTTTTTTTTGAGACA[A/G]AGTCTCACTTTGTCG	55159
rs561979192	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648532	AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGT	55159
rs562064986	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660407	GCAGTGAGCAAAGAT[G/T]GTGCCACGGGAATCC	55159
rs562065058	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654885	CTAATCCAGAGGAAG[G/T]CCCCAACTCTCTTTA	55159
rs562128219	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633020	GGTGTCTCACCTCTG[A/T]AATCCCAGCACTTTG	55159
rs562151730	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74660177	AGTGCTAACTCCTCT[A/T]TTCTATAGTTATGAG	55159
rs562199017	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74643629	TGTGTATGTTCTTTA[A/G]TATTTTTGAAGCATA	55159
rs562203853	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659998	AGGTCGAGGCTGCAG[C/T]GAGCTGTGATTGCAC	55159
rs562283470	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643960	GGGATTACAGGCGTG[A/C]GCCACCATGCCCGGC	55159
rs562319782	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664789	ATAAGTTCCTTTGTC[A/G]TGCAGGTCACATTTC	55159
rs562340625	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645349	CTGCTAGAGATACCT[C/T]ATGGATATATAGTCA	55159
rs562419933	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643924	CCTTGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA	55159
rs562533741	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625722	AGTTAGCGCTAGCTT[C/T]TAGAGTGGCACTATA	55159
rs562539721	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665004	GGATGTCACACAAAC[C/G]CTGTTTTTTATGTGT	55159
rs562557413	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648402	TCAGGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	55159
rs562557874	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74648729	GTGGTGAGCTGAGAT[C/T]GCACCACCGCACTCC	55159
rs562687034	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654791	TGAATGATAAGACAG[C/G]CTTATTGCTGATATG	55159
rs562697104	in-del	-/AGCC	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74627830	AGGGCTAGAGTTTAT[-/AGCC]AGCCACTCTCCTGAC	55159
rs562749685	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643388	GCATACACCACCGTT[C/T]ATTCAACTAAGCAAT	55159
rs562754606	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659987	TAAGCCTGGGGAGGT[C/T]GAGGCTGCAGTGAGC	55159
rs562833532	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664706	TTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGA	55159
rs562855007	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627521	AAGTAAGCTGATTCC[A/G]TTATTTCCTGTGTTT	55159
rs562892995	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646286	GAGGCTGAGGTAGAA[A/G]CATCACCTGAGCCCG	55159
rs562967201	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632116	CTAAGGTCGGCTGGG[A/C]GCAGTGGCTCACGCC	55159
rs562969807	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664264	CTAACTAAAAGCTTT[C/T]AATGTTTCTAGGGTA	55159
rs562970351	snp	A/C/T	4.9626e-05	0.00498106	synonymous-codon, missense	RFWD3	GRCh38.p7	16:74624012	AAATGGGCAGATGTC[A/C/T]AACACAGGCTGATCG	55159
rs563025676	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667435	AAAATACTTTGCCTA[A/C]ATAATCTCTTCAATC	55159
rs563076175	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637155	AAAAAACAACTTAAA[A/T]GGAGACAGGGTCTCA	55159
rs563128339	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74641821	ATCCCGGCTACTTGG[G/T]AGACTGAGGCAGGAG	55159
rs563130259	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647400	TCAAGTGACTCTCCT[C/G]CCTCAGCTTCCCGAG	55159
rs563294706	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662904	TTCAGAATGGTCATG[C/T]TTCTTTTTTTTTTTT	55159
rs563296665	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657181	TGAAGGTGCTCCAAT[C/G]CCTCTGGTGCCTGCC	55159
rs563363691	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635204	ATGGCATGAACCCGA[A/G]AGGTGGAGCTTGCAG	55159
rs563394186	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667262	TGACTCCTGCTGCTT[A/C]TCCCTAACGCTTTAG	55159
rs563402590	snp	A/G	0	0	intron-variant	RFWD3	GRCh38.p7	16:74630144	TCTGTTGCCCAGACT[A/G]GAGTGCAACGGCGCA	55159
rs563485825	in-del	-/GTTA			intron-variant	RFWD3	GRCh38.p7	16:74650323	CTATGCAAACTGGTT[-/GTTA]GAAAACAGTCTTGAG	55159
rs563501333	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666262	TCCCTGTTCTTTTAC[G/T]ACATGGGGAAACTTT	55159
rs563636659	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665832	GCTCACTGCAACCTC[A/G]GCCTCCCGGGTTCAA	55159
rs563679821	snp	A/G	1.64817e-05	0.00287064	intron-variant	RFWD3	GRCh38.p7	16:74649229	TTTCCAGAAATGACA[A/G]GAGAGGTAAAATACA	55159
rs563710308	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649904	TGGCTGACTGCTTCT[G/T]CATGAAATTAACTTT	55159
rs563755655	snp	A/G	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74635049	ACTTTGGGAGGCCGA[A/G]GCGGGCGGATCATGA	55159
rs563828339	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627575	CACCTGACCAACACA[A/C]CTGAACCTAACTTGT	55159
rs563849958	snp	A/G	1.65132e-05	0.00287339	synonymous-codon	RFWD3	GRCh38.p7	16:74628471	CCTGTAGGTCACAAG[A/G]CAGTGCCGGGAGCTG	55159
rs563896191	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74628222	TGGCTAATTCACTTC[A/C]AGGAGTACCTGGCAG	55159
rs563930964	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655396	AGGCACCCGCCACCA[A/C]GCCTGGCTAATTTTT	55159
rs563948019	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661685	TTAGAAAACATGAAG[A/C/T]CCTGTGATCATAGTA	55159
rs563997128	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634306	ACCAACAAAAACCAA[C/T]AACCTTTTAAAACTT	55159
rs564012368	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634181	AGGAATAGTGAACAA[C/T]AGAGAATGAAAATAA	55159
rs564021246	in-del	-/AA	0.0154538	0.0865337	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621099	CTGACCAACATGCTG[-/AA]AAACCCGTCTCTACT	55159
rs564110304	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74639244	GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTCAA	55159
rs564180571	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74639649	AATCAAGATCCCAAA[G/T]GTGTTTTTCATGGAA	55159
rs564215461	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634891	TCATGCCTGTAATCC[C/T]AGTACTTTCGGAGGC	55159
rs564225120	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659851	AACATGGGTAATAGA[C/T]GACCTAGCTACCACT	55159
rs564265567	in-del	-/TTT			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663236	AATCATCAAAGCAGA[-/TTT]TTAAACCACCTGAGG	55159
rs564295416	snp	G/T	0.0107246	0.0724382	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623147	TGAGATCCTAAGCTG[G/T]CTAGAAAAAACAAAA	55159
rs564298799	in-del	-/TTT	0.454423	0.143914	intron-variant	RFWD3	GRCh38.p7	16:74639037	GCATTGAGCTAAGAC[-/TTT]TTTTTTTTTTTTTTT	55159
rs564299095	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74665251	CTGGTGTTCCAGACC[A/G]GCTTGGGCAACACAG	55159
rs564315306	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74657981	AAGTGATAGACGATT[-/A]AAAAAAAATCACTCT	55159
rs564331267	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644031	TTACATTGCACTGCA[C/T]GTGCAAAGCTTCACT	55159
rs564341481	snp	C/G/T	4.94257e-05	0.004971	synonymous-codon	RFWD3	GRCh38.p7	16:74649180	TGTAACTTCTTGCTC[C/G/T]GCTGAGACACCTGCT	55159
rs564372298	snp	A/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74638411	AAATATTAACAAAGG[A/T]AAGACCAATTAGAAT	55159
rs564466014	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74655299	GGTTAGAGTGCAGTG[C/G]CGTGATCTCGGCTCA	55159
rs564512263	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655881	ACAGCTTATCTGTTT[A/G]GAGTATGTCTTACAA	55159
rs564594113	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638286	TGTTAAAAGGCCAAG[A/G]TTACTGGATTAAAAA	55159
rs564668844	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633597	TGACTGCTGGGGATG[A/G]GAGAGGAGGGAGGGG	55159
rs564695005	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668168	GTAATTTCAGCGAGT[A/G]CTCCCATAGCTGAAA	55159
rs564695011	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662984	ATCTCGGCTCACTGC[A/C]AGCTCCGCCTCCCGG	55159
rs564722879	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660028	CCACTGCACTCCAGC[C/G]TGGGGAGCACAGTGA	55159
rs564735490	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653073	GCTAGCTGCGATGAC[C/T]CATGTCTGTAATCCT	55159
rs564738667	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621082	CAGAAGTTTGAGACC[A/T]GCCTGACCAACATGC	55159
rs564776869	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633182	TTCAGGAGGCTGAGG[A/C]AGGAGAATCGCTTGA	55159
rs564831856	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667801	AGCAAGGAACAGAAT[A/C]AAGATCGTCTCCTTC	55159
rs564953740	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74657717	GACCTCAGGTGATTC[A/G]CCTGCCTCAGCCTCC	55159
rs564993427	snp	C/T	0.0185938	0.0946107	intron-variant	RFWD3	GRCh38.p7	16:74645750	CAAATATTTTCTTTT[C/T]TTTTTTTTTTTTTTT	55159
rs565070292	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631165	GGCCACAGGTTTTCC[C/T]CTTGAGTTCTAAGGA	55159
rs565081320	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646290	CTGAGGTAGAAGCAT[A/C]ACCTGAGCCCGGGAT	55159
rs565111408	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74624555	CATCCACCACCACGC[C/T]CGGCTAATTTTCTTG	55159
rs565118247	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74626590	TGCTGCACCATGGGG[A/G]CGCTACACAAAAAAT	55159
rs565144408	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74650904	TGAAAAAAAAAACAA[A/C]AAAAAAACCCACTTC	55159
rs565187340	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74630598	CTCCATCATATGAAA[C/T]AGCATGAATACAAAC	55159
rs565278049	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74640483	AGCAATGAAAATTTG[G/T]ACAGAAAAATATACT	55159
rs565396122	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74631028	AAGATGTAAAGATTA[C/T]CATTTAAATGATCAT	55159
rs565418001	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632129	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	55159
rs565432958	snp	A/C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650783	TCAGGTGGCTGAGGC[A/C/G]GGAGGATCGCTTGAG	55159
rs565510245	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630387	ACAGGCGTAAGCCAC[C/T]GCACCCAGCGACATG	55159
rs565545415	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74649633	TTATTATACCTAACA[A/G]TATTAACAATAATCC	55159
rs565555552	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662298	ATCAGTATAACTTAT[C/T]CCCTTAATTACTTTG	55159
rs565616710	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657138	CACCAACAGGTCATA[C/T]AAAGATAATTCTCTG	55159
rs565669773	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645554	TGGTGGGTTTCACCA[C/T]GTTGGCCGGGCTGGT	55159
rs565760723	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650395	GGGGGGCTGGTGTGT[G/T]TGTGTATACAGTACT	55159
rs565844835	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622745	TTCTGTTGTGGAAGT[A/G]GGTTGGCAAAGTAGT	55159
rs565861595	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623174	AAAATCTTCCCCACC[A/G]CTCAAACAACTGGCC	55159
rs565936536	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649300	CCTGACTCACTACAG[C/T]TTCCCATTTCTAACT	55159
rs565954150	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74635005	ACTAGGCATAGCCGG[A/G]CGCGGTGGCTCACGC	55159
rs565959512	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668387	AGGAAATGTTCCCCT[A/G]TGAAGCAACTACACC	55159
rs565968705	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666589	CAACCCAGATACGCG[A/C]GGGGGTTCGGGCTCC	55159
rs566050457	snp	C/T	1.64974e-05	0.00287201	missense	RFWD3	GRCh38.p7	16:74636552	TGTAAATTCTGACTT[C/T]GATGTGACGTAAGTT	55159
rs566125472	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644775	AAATTAGAGAAAATG[A/T]AAAATCAATCTTGAA	55159
rs566187681	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667664	TGATAAAGACGATCT[A/G]GATGTAACAGAACTC	55159
rs566595666	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630728	GACGATTAACACAAT[A/T]ATAAGCCAAGAGAAA	55159
rs566662822	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74633847	CCCAGTTACTCAAGA[A/G]GCTGAGGTGGAAGGA	55159
rs566697553	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74642272	GCATTACAGGCACGC[A/G]CCACCACATCCGGAT	55159
rs566701477	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74647665	GACGCTATTTGGGCT[C/G]ACTGCAACTTCTGCC	55159
rs566706419	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636066	GTTGAGGACATATAA[A/G]TCCTTCTTGGACTAT	55159
rs566746851	snp	C/G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624686	ACAGGCGTGAGCCAC[C/G/T]GCGTCTGGCCTCTAA	55159
rs566769659	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658446	GTGAGTCAAAAGCTG[C/T]TCACCTTGGCCCAGG	55159
rs566788674	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645914	CCTGCCACCAAGCCC[A/G]ATTTTGTGTATTTTT	55159
rs566816262	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657874	GACTAAACACATAAG[A/G]AAAGCATTTCATAAG	55159
rs566951107	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663066	CCTGCCACCACGCCT[A/G]GCTAATTTTTTGTAT	55159
rs566969037	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624370	GGTCAATAAGATAAA[A/G]TCCCTGTCTTTGCCC	55159
rs567040526	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667579	GAGGAGCGCGAGCCC[A/G]CAGCCGTCTCGGCTC	55159
rs567052832	snp	C/G	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74661120	AGATGCTGGGATGGT[C/G]TGATTACCATCAGAT	55159
rs567066251	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663227	TGTTTCTTAAAATCA[C/T]CAAAGCAGATTAAAC	55159
rs567213292	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646995	GGGAGGCTGAGGCAG[A/G]AGAATGGTGTGAACC	55159
rs567245252	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628230	TCACTTCCAGGAGTA[C/T]CTGGCAGAATATGCT	55159
rs567257297	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636866	CATGCACCCACTACC[A/C]TGCCCGGCTAATTTT	55159
rs567262438	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646338	CTATGATTGTGCCAC[C/T]GCACTCCAGCATGAG	55159
rs567328147	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648108	TGCCACCACACCTGG[C/T]GAATGTGCTTAATAA	55159
rs567332358	snp	A/G	0.00517822	0.0506191	intron-variant	RFWD3	GRCh38.p7	16:74641306	TAGCTGGGACTACAG[A/G]TGCGTGCCACCATGC	55159
rs567337420	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663016	TTCACGCCATTCTCC[C/T]GCCTCAGCCTCCCGA	55159
rs567375851	snp	A/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74635481	CAAAAGAAAAAAAAA[A/T]AATCAACAAGGTAAC	55159
rs567415563	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624237	AAGTCAGCACACCTG[A/G]CATAGTTCAGGTACA	55159
rs567418365	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641996	ACTTTCTATATCATA[C/G]TATGTATAATTTACA	55159
rs567501576	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667843	CTTCTTCAGCAGAAA[A/G]TACAAGGCAGAATGG	55159
rs567529673	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630694	GATTTCTGACTAACT[C/G]TGGAACACCCACTGA	55159
rs567532946	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640624	CTCTGGCCTTTGTGA[C/T]AGAGCAAGACCCTGT	55159
rs567563272	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653425	GTTTGAGGCCACAGA[A/G]AGTGAGCGAGCTATG	55159
rs567630608	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623874	CTTGGGGCTGCTAGG[C/T]GCTAGCAAACAACAT	55159
rs567687277	in-del	-/AGC	0.00438332	0.0466095	cds-indel	RFWD3	GRCh38.p7	16:74623328	GTGTTATTGCCACAA[-/AGC]ACACCCAGGTGTGCT	55159
rs567743853	in-del	-/TGCCAAAGT	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74629241	CTATGAAGTCGTTCG[-/TGCCAAAGT]TGCCAAAGTGTCTAC	55159
rs567788004	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667035	GTAGTTCGTCCTGAC[A/G]AGGCGGGACCGCGCT	55159
rs567898829	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638384	TAAAAAGAGCAAAAG[C/T]AGACATCAAGCAAAT	55159
rs567900848	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632821	AATTCTCTAGTGTTA[C/G]AATTTATTCATTTAT	55159
rs567925373	in-del	-/AAC			intron-variant	RFWD3	GRCh38.p7	16:74632411	AACAAAACAAAACAA[-/AAC]AACAACAACAACAAC	55159
rs567959773	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621262	AGCTAGGGCTACAGA[A/G]CAAGATTCCGTCTCA	55159
rs568003626	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74665950	TGATCCGACTGCCTC[A/G]GCCTCCCAAAGTGCT	55159
rs568056620	snp	C/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74665405	CAATATGGTGAAACC[C/G]CGTCTCCACTAAAAA	55159
rs568071116	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626801	CTACAATAGCTTTTT[A/G]CTTAAGAGAAAAACA	55159
rs568080331	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621821	TGCCTCAGCCTCCCA[A/T]GTAGCTGGGACTACA	55159
rs568341527	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74652177	ACTATCATCACAAAA[A/G]CAATCTATAGTGATT	55159
rs568355375	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74658241	GTGTTATTCACCAAT[A/T]TATCTAGGGCAAAGT	55159
rs568392027	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643715	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	55159
rs568400636	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74638328	GCTGTTGGTTGTTCA[A/T]GAGATACTCAAATAA	55159
rs568486403	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664927	TGAAGCTTCCTAACC[A/G]CTGTAGGCCAGTCGG	55159
rs568544253	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659680	ATCCTTGATGGGCAC[C/T]ACAGACACTGGAGCC	55159
rs568544323	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74653429	GAGGCCACAGAGAGT[A/G]AGCGAGCTATGGTTG	55159
rs568699213	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632161	TTCAGGAGGCCGAGG[A/C/T]GGGCGGATCATGAGG	55159
rs568725304	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642893	CTGTATCGGCATTTT[A/G]AAACTCTTCACTTTT	55159
rs568730458	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663738	ATAAAGGAGAAACTG[A/G]TGATTGATGACTGCT	55159
rs568814502	snp	A/G	5.22098e-05	0.00510903	intron-variant	RFWD3	GRCh38.p7	16:74637997	AAGCCAGCAACAAGT[A/G]GGGATTAGGAAGGCT	55159
rs568835203	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663379	AATGTGGTGTCTTGG[A/T]AAAACAATGTTTCAA	55159
rs568836357	snp	A/C	1.83185e-05	0.00302637	intron-variant	RFWD3	GRCh38.p7	16:74661475	ACAGTATTTGTAAAA[A/C]GTATTAATAAAATAG	55159
rs568913156	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74647074	CCTGGGTGACAGAGC[A/G]ACACTCGTCTCAAAA	55159
rs568941961	snp	A/C/G	1.6534e-05	0.00287519	missense	RFWD3	GRCh38.p7	16:74628637	GCTGAGGCAGCTCTG[A/C/G]GCATGTATGACAGGG	55159
rs569137250	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74639037	GCATTGAGCTAAGAC[-/TT]TTTTTTTTTTTTTTT	55159
rs569140262	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657806	AGTGCTAAGCAAGTT[C/T]ACCAACTCCATTTCT	55159
rs569192219	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652829	GGAGTTTGAGGCCAC[C/T]TTTGTCACAGAATTA	55159
rs569326282	in-del	-/TTCT	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662905	TCAGAATGGTCATGC[-/TTCT]TTTTTTTTTTTTTTG	55159
rs569331252	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658529	CACACTGAGAAATTC[A/C]TCTCAAGAAATTCAG	55159
rs569332596	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631518	CCAACACTCTGGTAT[A/G]TAACATTTTTCTACC	55159
rs569427618	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642438	CCTTCTACTGAATCT[A/G]TAATTAACTTCTTCT	55159
rs569471829	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74644214	GAATTATAAATAACA[C/G]TGTAAGACAGACTGC	55159
rs569475233	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668264	TTTCCTATTCTGCCA[C/G]TCACTGAATTCTCAG	55159
rs569491368	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636144	TTATCAGTATTTCTA[C/T]CCTCTTGGTTAATAA	55159
rs569495124	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621986	ATCCAAATTTAATGT[A/C]CTAATGCAAGGACTG	55159
rs569509872	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663621	CCTAAAACCCACGAA[C/T]ATGACCCCCACAACC	55159
rs569546958	snp	G/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664770	GAAAAAAGAAAGAAA[G/T]AAAATAAGTTCCTTT	55159
rs569581697	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667953	ACAGGGGAGTAAAGA[C/G]TCCAGTAACCCTCAA	55159
rs569627775	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656272	GATCACACCACTGTA[C/T]TCCAGCCTGGGCAAC	55159
rs569687996	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649494	GCCAATCTTGTTCCA[C/T]CTAAGCCCCCATTCC	55159
rs569783556	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627253	TGCCTGACTGTTACA[A/G]ATGTGTTTAATACAG	55159
rs569880879	snp	C/T	6.65923e-05	0.0057699	missense	RFWD3	GRCh38.p7	16:74661364	GCTGGTCCCCCTTGG[C/T]TGCTGGCCATGCCAG	55159
rs569917078	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639313	AAAGTGCTGGGATTA[C/T]AGGTGTGAGCTACTA	55159
rs570014180	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660104	AAACAAAGGGATTTC[A/G]TCGAAGCTTCCTCCA	55159
rs570050535	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74626541	CACACTTCGTATGGT[A/G]GTGTGATTTTTATCT	55159
rs570111055	snp	A/C	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74655073	TAAGACAATTGATGA[A/C]AGTATCTACACTAAA	55159
rs570117492	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649044	TTATGACTGCACCAC[C/T]GCACTCTAGCCTGGG	55159
rs570124676	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648859	GGGAGGCCGAGGCAG[A/G]ACGATACCTTGAGCC	55159
rs570142060	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661641	TCCTCTCTATAACAA[A/G]CATTTATAACCAGTT	55159
rs570152660	snp	C/T	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74643822	CTGGGATTACAGGCG[C/T]CCGCCACTATGCCCG	55159
rs570190699	snp	A/G	0.0236746	0.106192	intron-variant	RFWD3	GRCh38.p7	16:74644094	GGGGGGTGGTCAGGG[A/G]TATGAGAAGCAAAAA	55159
rs570297015	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627031	GCAAACAAAAGCAAG[A/G]TAACAAAATAGGACC	55159
rs570310257	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655707	TTGTTGTATTTTTAG[C/T]GGAGACGGGGTTTCA	55159
rs570328718	in-del	-/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74646417	TATAAAGAAAAAAAA[-/T]ATTATTACCCTCCCA	55159
rs570328890	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654343	TTATTATTTCTTTCT[C/G]TCTGCCTGTGTTGGG	55159
rs570448296	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74656106	TCACACCTGTAATCT[C/G]AGTACTTTAATGAAA	55159
rs570459798	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633451	CCCGTTAAAAAGGAA[G/T]TAACTACTAATATAT	55159
rs570463734	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621883	TGTATTTTTAGTAGA[C/G]ATGGGGTTTCACCAT	55159
rs570610426	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638426	AAAGACCAATTAGAA[C/T]TAAGGAAAAAGCATA	55159
rs570630221	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665434	AATACAAAAACTACC[A/C]GGGTGTGGTGGCGCA	55159
rs570690593	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74666032	TTATAACAGGAAAAA[A/G]GGAGGAAGAGAGAGG	55159
rs570771058	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638907	AGCCTACTACACACC[C/T]AAGCTATATACTGTT	55159
rs570774393	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643785	GGTTCACGCCATTCT[C/G]CTGTCTCAGCCTCCT	55159
rs570798921	in-del	-/CACAC			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621147	CCGAGCATGATGGCG[-/CACAC]CTGTAATCTCAGCTA	55159
rs570913355	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659704	TGGAGCCACAGTCAT[A/G]GCAAGCCCCAACATT	55159
rs571117797	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659171	CCTTAAGTTGGTTAA[C/T]ACAAGTCACTGTGCT	55159
rs571133679	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625379	TACACAAATTAGCCG[C/G]GTATGGTTGGTGTGC	55159
rs571172425	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626004	CAGCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC	55159
rs571233549	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644764	AGAATATATTCAAAT[C/T]AGAGAAAATGTAAAA	55159
rs571239039	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651868	TAGCCTTCCGAAATT[A/T]AAGCTTCATGGATGT	55159
rs571282210	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667019	GTGCTCTCATTGGCT[A/G]GTAGTTCGTCCTGAC	55159
rs571343565	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74661995	AAACTTTATCCTATC[C/G]CTTTCATTATTTTTG	55159
rs571360821	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663574	GTGGACGAAGTACAT[A/G]TATGTATCTTTCTCT	55159
rs571394515	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646497	ACATGATAAGAAAAA[G/T]AATTAATTCGCTGGG	55159
rs571396395	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74640810	CAGGCGTGGTGGCGG[A/G]TGCCTGTAGTCTCAG	55159
rs571450081	snp	C/T	0.00914312	0.0669923	intron-variant	RFWD3	GRCh38.p7	16:74656956	GAAGATGTGACTGAA[C/T]TGATCTCATTCCTAG	55159
rs571524329	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645361	CCTCATGGATATATA[A/G]TCATGCATTGCTTGA	55159
rs571532932	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630253	GGCGTGTGCCACCAC[A/G]CATGGCTAACATTTT	55159
rs571568630	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623766	GATACACAATCTGTA[A/G]TGTCTCAGTGACCTA	55159
rs571577799	in-del	-/CTGAC	0.00358779	0.0422022	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622703	CCCATGAACAGGACA[-/CTGAC]CTGACCTGCCCACAT	55159
rs571590941	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649427	AGTACACAGAACAGT[A/G]TAGTTAAGCCACAAG	55159
rs571636746	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644872	CACTTGTAACACCTA[C/T]GAATCACTTGTCATT	55159
rs571647470	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629559	AGCTACTCGGGAGGT[A/G]GAGGATGCAGTGATC	55159
rs571949114	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646429	AAATATTATTACCCT[A/C]CCAAGTAGTTGAGAC	55159
rs571964890	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74640249	CTCCCGAGTTCAAGC[A/G]ATTCTTCTGACTCAG	55159
rs571991364	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666842	AGACTCGGTAGTTAC[A/C]TCGGCCGCACTCCGA	55159
rs572022052	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74635443	CTGCACTCCAGCCTG[C/T]GCAAAAGAGTGAGAC	55159
rs572225133	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74656327	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG	55159
rs572246420	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627036	CAAAAGCAAGATAAC[A/G]AAATAGGACCCCCAG	55159
rs572281314	snp	A/G			utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666856	CCTCGGCCGCACTCC[A/G]AATGCACCTACGCCA	55159
rs572288626	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649685	GGCATCCAGTTCATA[C/T]TCAAAATTTCCCAAT	55159
rs572335787	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621663	GTGATGTCCTACAAC[A/G]GGGACTGGGAATGGC	55159
rs572363062	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74655822	TGAGCCACCACACCC[A/G]GCCTATGTCTGTGCT	55159
rs572392128	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628022	TCAGCTGGCTGGGCA[C/T]ACACAGCCACTGTTG	55159
rs572456694	snp	G/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74665636	TGGTGGCGCGCACCT[G/T]TGGTCCCAGCTATTG	55159
rs572497108	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627282	AGTTGTTACCTCAGC[A/G]TCTGTTTTTAGGGCT	55159
rs572528961	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633547	TTATGTAAAATTCTA[A/G]AAAATGCAAACTCAT	55159
rs572611673	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668428	AGTGCTAGTTGCCGC[A/C]GAACAATCAAAGGAG	55159
rs572645640	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643348	AGGACAACATATGCA[C/T]ATTTCAACATTGTAT	55159
rs572677922	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624557	TCCACCACCACGCCC[A/G]GCTAATTTTCTTGTA	55159
rs572694645	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74648645	GGCGGGGTGGCGTGT[C/G]CCTGTAGTCCCAGCT	55159
rs572733229	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74643867	ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	55159
rs572754208	snp	A/G			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662376	GGGGTTCAACTAATA[A/G]TTATTAAGCACCTGT	55159
rs572771781	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657544	GTAGTGGCGCAATCT[C/T]GGCTCACTGCAACAT	55159
rs572856517	in-del	-/AG	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74629609	TCCAGCCTGGGTGAC[-/AG]AGTGAGACACCATCT	55159
rs572858896	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651278	TACTAGGACTTGAAA[C/G]TGTCAGCCTAGACAG	55159
rs572862498	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74624899	CAAGAGGCTGAAGGA[C/G]GATTGCTTAAGCTGA	55159
rs572933913	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631129	GGTAACTCCTTTAAA[C/T]TCCATAACATTTGTT	55159
rs572941309	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624549	TACAGACATCCACCA[C/T]CACGCCCGGCTAATT	55159
rs572965308	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659467	AAGCCTGCTGGTGCA[A/C/T]GCCTGCAATCCCAGC	55159
rs572996784	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74650856	CACTCCAACCTGGGG[G/T]ACAGAGTGTAACCCT	55159
rs573020931	snp	A/C	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631850	GGTCTCAAACCCCTG[A/C]CCTCAGCTGATTGCC	55159
rs573076692	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642929	TGAGGCTGGAGAGTA[C/T]ACTAATTCCTTATTG	55159
rs573085438	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74641011	AACAAGAAAAGTTTA[A/C]GTTAGAAAAGTAATT	55159
rs573087856	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641351	TATTTTTAGTAGAAA[A/T]GGGGTTTCACCATGT	55159
rs573094807	snp	C/T	1.65968e-05	0.00288065	intron-variant	RFWD3	GRCh38.p7	16:74636319	GTCTAATAAAGAACA[C/T]GAAAGCTGAGGTTCT	55159
rs573132788	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657115	GCAAATGGGGTTTTC[C/T]AGAGAACCACCAACA	55159
rs573158048	snp	A/C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635152	GGGTGTGGTGGCGGG[A/C/T]GCCTGTAGTCCCAGC	55159
rs573159911	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629297	CCCTGTCACAATAAA[A/G]GTAATCAAAGTAAAC	55159
rs573191834	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643972	GTGAGCCACCATGCC[C/T]GGCCCTAGCAACTGT	55159
rs573197106	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74646180	AGGAGTTTGAAACCA[A/G]ACTGGACAACATAGC	55159
rs573237407	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74637536	AGATGCTGAGGCTGA[C/G]GCAGGAGAACCGCTT	55159
rs573356936	snp	A/T	0	0	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662162	AAATTTTTTTTTGTT[A/T]TATAGATGAAGGCTT	55159
rs573371329	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623464	ACTGAATAATACTCT[C/T]TTACATCTACGTTGC	55159
rs573477294	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74630099	CTAGACATGTGGCTA[-/T]TTTTTTTTTTTCTTG	55159
rs573489237	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667116	CGCCCCGGAAAAAAT[G/T]GGAGGTTTTTTTGTT	55159
rs573518199	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659468	AGCCTGCTGGTGCAC[A/G]CCTGCAATCCCAGCT	55159
rs573586360	snp	A/C	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663282	GAGGGCTGAAGACTA[A/C]AGTCAGAGACACTAC	55159
rs573648030	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662908	GAATGGTCATGCTTC[C/T]TTTTTTTTTTTTTTG	55159
rs573650891	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656991	TCCTTTCCTTCTTAT[C/T]GGTTAGTTTATTGCT	55159
rs573691157	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74626232	GGATTACAGAGCAGA[A/G]CTTACACTTTTTTGC	55159
rs573739766	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635794	ATCTGCAAGATTTAG[A/G]AATGATTTAATTGAG	55159
rs573785334	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662103	ATCTTTAATTCCATT[G/T]TATCAGTTTGAAAAC	55159
rs573787616	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74656534	GTCACCCAGGCTGGA[A/G]TGCAGTGGCATGATA	55159
rs573840009	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74640558	CCCAGCTACTCAGGA[C/T]GCTGAGGTTGGAGGA	55159
rs573876885	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645663	CAGCCTGGTATTATC[A/G]TCTAATGGGACAACC	55159
rs573879618	in-del	-/AGGAAATAAAT	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74636286	ATTTTCCAAAAGGCA[-/AGGAAATAAAT]ATATGGAGTCTAATA	55159
rs573882019	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74641715	TGATCACGAGGTCAG[C/G]AGTTCCAGACCAGCC	55159
rs573903103	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640881	GAGGTGGAGGTTGTA[A/G]TGAGCTGAGATCACG	55159
rs573904270	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649940	ATAATAAATTGAGCA[C/T]TGTGCAACCACCACC	55159
rs573916365	in-del	-/CTT			intron-variant	RFWD3	GRCh38.p7	16:74649899	GGATTTGGCTGACTG[-/CTT]CTTCATGAAATTAAC	55159
rs573926828	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661618	CAGAAGTGTTTGGTA[A/G]TGGACTTTCCTCTCT	55159
rs573993147	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650778	GCTACTCAGGTGGCT[G/T]AGGCGGGAGGATCGC	55159
rs574018615	snp	A/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74640415	TCCCAAAGTGCTGGG[A/T]TTACAGGCGTGAGCC	55159
rs574076360	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74666062	GGAGAGGGAGAGGCG[A/G]AGGGGGAAGAGGAGG	55159
rs574152588	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622970	GACAAGTTCTTCTCA[C/T]GTTTTCAATAGCAGT	55159
rs574187323	snp	A/G/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74654028	GTTCAATTCAGTGTT[A/G/T]TTTTTTTTTAGCATA	55159
rs574188650	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659791	CCAATTCCAGCCTTA[C/T]CACAACCAAATCACA	55159
rs574212465	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634187	AGTGAACAATAGAGA[A/G]TGAAAATAAATAATT	55159
rs574222048	in-del	-/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74666267	GTTCTTTTACTACAT[-/G]GGGAAACTTTGGGCG	55159
rs574298255	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74628340	GCTACAACACACCTC[A/G]TTAGCCTGTGAGCGG	55159
rs574321219	snp	A/C			intron-variant, splice-donor-variant	RFWD3	GRCh38.p7	16:74661955	CAAAATGGAAACTTA[A/C]CTAATGTTTCCAAAA	55159
rs574357352	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648184	TTGTTGGCTAGACAG[C/G]ACAGGTTATCCTCAA	55159
rs574444181	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626205	TCACATACACACATA[A/T]GCGGATATGTGGGAT	55159
rs574512725	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664565	CAGCCTGGGCAACAC[C/G]GCAAAACCCCGTCTC	55159
rs574517062	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637099	GTTGAAAGTCCTTAA[C/T]GGTGGTTTCGTTTAA	55159
rs574603596	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74664955	CGGAGGTGCCTAGAA[C/T]GAGAGACCATGGGCT	55159
rs574609533	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74640147	ACATGGAAACTTAAT[-/T]TTTTTTTTTTTTTTT	55159
rs574638632	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632054	CTAAAAGCAATATAT[C/T]TTAAATGGATCTCAG	55159
rs574800222	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642469	TCTTTAAAATTTTCT[C/T]TCCTTTTTTTCCTTC	55159
rs574849626	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74647449	CGCACCACCATATCC[A/G]GCTAATTTTTGTATT	55159
rs574869741	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642240	CGATTCTCGTGCCTC[A/G]GCCTCCCGAGTTGCT	55159
rs574978695	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74633341	TCATGACAATGAAGA[C/G]AAGAAGAAAAAAAAA	55159
rs574986645	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74646681	GTTCCAGCTACTCGG[A/G]AGACTGAGGCAGGGG	55159
rs575002442	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624490	AACATCTGCCTCCTG[A/G]GTTCCAGCGATTCTC	55159
rs575102288	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652927	CTCAAATGATCCACC[A/C]ACCTTGGCCTCCCAA	55159
rs575128438	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74653077	GCTGCGATGACTCAT[A/G]TCTGTAATCCTAGCA	55159
rs575178504	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74642183	GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTTAC	55159
rs575181258	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668208	CTTCAAACAACGAAT[A/C]CTTAATTGTCAATAG	55159
rs575234964	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641655	TCTGGCCGGGTGCAG[C/T]GCCTCACGCCTGTAA	55159
rs575309887	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646310	GAGCCCGGGATATTG[A/C]GGCTGCAGTGAGCTA	55159
rs575310459	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668480	TCAGTGATTTGAGGA[C/T]GGAGGAGTCGTTTTC	55159
rs575365541	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624922	TAAGCTGAGGAGTTT[A/G]AGGCTACAGTGAACC	55159
rs575453949	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625538	AAAAAGGACAGACCA[A/G]GCGCAATGGCTCACG	55159
rs575474720	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74637008	GTGAGCCACCGCGCC[C/T]GGCCAGAACTGCTGA	55159
rs575485124	snp	C/G/T	9.88381e-05	0.00702929	missense	RFWD3	GRCh38.p7	16:74636468	TTTTGGAAGTGGTAC[C/G/T]TGTGCTTGTGCTGGC	55159
rs575488680	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630397	GCCACCGCACCCAGC[A/G]ACATGTGGCTATTAA	55159
rs575512378	in-del	-/CA	0.000215137	0.0103693	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623923	TCAAGGTTTCGAGAC[-/CA]CAGTCACTCCCACTT	55159
rs575521897	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631176	TTCCTCTTGAGTTCT[A/G]AGGAAATAAAATAAT	55159
rs575649399	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74652192	ACAATCTATAGTGAT[C/T]TGAAGTAAATCCTAT	55159
rs575654375	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639132	CTACCTCCGCCCCCC[A/G]GGTTCAAGAGATTTC	55159
rs575699023	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74638245	TAGTGTTCAGCTACG[A/G]CAAATTGTAAAAGAT	55159
rs575786073	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657905	AAGATTTAATCAAAT[A/G]CATACTAGAGTTAGG	55159
rs575887194	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620901	GGGAATCGCTTGAAC[A/C]CGGGAGGCAGAGGTT	55159
rs575959954	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664003	TTCTCCCCCTATGCA[C/T]GAGAAAACTGGAGGT	55159
rs576003467	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632459	TCATCATAACACCGA[C/T]ACGAATTCCATGCTA	55159
rs576135292	snp	A/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623665	AGAATTTCCAACATA[A/C]AATAATGGTTAATGA	55159
rs576169134	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648738	TGAGATCGCACCACC[A/G]CACTCCACCCTGGGC	55159
rs576192148	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74645637	GGATTATAAGTGTGA[A/G]CCACTGCGCCCAGCC	55159
rs576325804	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632756	TCAAGTAGCTCCTTC[A/G]TCCACCTTTCTTGGC	55159
rs576488568	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632950	GGGATTACAGGCATG[A/T]GCCACCACACCTGGC	55159
rs576508539	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648315	GCAAGCTTCCCATTT[G/T]AACCTGCAGCCCCAC	55159
rs576602366	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74650486	CCTATTTTTTTAAGA[A/T]GCTAAGATTGACCAA	55159
rs576663581	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647738	CTGGGATTATATGCG[C/T]CTGCCAACATACCCA	55159
rs576679522	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632876	TGCAGTGGCGTAACC[C/T]CAGCTCACTACAACT	55159
rs576731457	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667443	TTGCCTACATAATCT[A/C]TTCAATCTCAAACCG	55159
rs576733433	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637772	TGGCAAATCCTATTT[C/G]TTTCTGAGATGAACA	55159
rs576844030	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621300	AACAAACGAACAAAC[C/T]CGAGAAATCTACCAG	55159
rs576868372	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655179	ATGCCTGGCTTCAAG[G/T]CTCAAAGGACAGGCT	55159
rs576936085	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74659920	CATCGGCATGGTTGC[A/G]TATGCCTGTAGTCCC	55159
rs577000384	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660218	AAGCCCTCTCTGAGC[A/G]GAGATCGCACCACTG	55159
rs577231652	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630121	TTTTTCTTGAGATGG[C/T]GTCTCACTCTGTTGC	55159
rs577259816	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642557	CCAGGCTAGAGTGCA[A/G]TGGCATGACCATAGC	55159
rs577372746	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642269	CTGGCATTACAGGCA[C/T]GCACCACCACATCCG	55159
rs577518437	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647690	TCTGCCTCCCAGGTT[C/T]AAGCGATTCTCCTAT	55159
rs577582852	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635701	TTAGATGGGATAAAG[A/G]AACATTATATAACCA	55159
rs577607393	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74653048	GGACACACACACACA[A/G]ACACATTAGGCTAGC	55159
rs577634840	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665849	CCTCCCGGGTTCAAG[C/G]GATTCTCCTGCCTCA	55159
rs577657616	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640337	TCTTAGTAGAGACAC[C/G]GTTTCATCATGTTGG	55159
rs577676843	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667151	TTTTGTTTGGTTTTT[G/T]TTTTTTTTTTTAGCG	55159
rs577693984	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635201	AGAATGGCATGAACC[C/T]GAGAGGTGGAGCTTG	55159
rs577760859	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667622	CGGCAGGAAAGCCAC[A/G]AAGAAAACTGATAAA	55159
rs577864740	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666236	GATTGATTAGATACA[C/T]AGATATTAAATCCCT	55159
rs577872028	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650535	CCCTGGTCCCTGTAT[G/T]AAAAGGAATCCCATC	55159
rs577876204	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645154	GAGACCATTTTTCAT[C/T]TATCAGACTGGTATA	55159
rs577908121	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74644287	TCACTACGAGTGACT[C/G]ATAACTTCTTTTTCA	55159
rs577914992	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645627	CAAAGTGCTGGGATT[A/G]TAAGTGTGAGCCACT	55159
rs577944522	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74661559	TTTAATATCATTCTT[A/C]GCAAGACTGAGAAGC	55159
rs578041008	snp	G/T	3.29451e-05	0.00405851	synonymous-codon	RFWD3	GRCh38.p7	16:74661038	TTGAAGATGAAGGTC[G/T]CAGGAATTCCAGCAT	55159
rs578171875	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74628955	TTACTATGAAGCTTG[A/G]CTGATGTGAAGCTTC	55159
rs578181923	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638597	AAGATGAAAATTGGA[A/G]AAGATAAAGCTGCCC	55159
rs578219739	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639125	CTCACGGCTACCTCC[A/G]CCCCCCGGGTTCAAG	55159
rs578244755	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74632299	CGGGAGGCTGAGGCA[C/G]GAGAATGGCCTGAAC	55159
rs745338388	snp	C/G	1.68687e-05	0.00290414	intron-variant	RFWD3	GRCh38.p7	16:74630974	TGTGGAGTTACAAAA[C/G]ACTTTTACAACTGCA	55159
rs745341659	snp	C/G	1.64727e-05	0.00286986	synonymous-codon	RFWD3	GRCh38.p7	16:74644409	AGCTCTCAGGGTTCG[C/G]GCATAAAGGACGACA	55159
rs745382903	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74629339	TGAACATTACATACA[A/T]ATATTCTTTCCTTGC	55159
rs745477537	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662930	TTTTTTTTGAGATGG[A/T]GTCTCGCTCTGTTGC	55159
rs745480819	snp	A/G	3.68636e-05	0.00429307	intron-variant	RFWD3	GRCh38.p7	16:74661478	GTATTTGTAAAAAGT[A/G]TTAATAAAATAGATA	55159
rs745482501	snp	A/G	3.29777e-05	0.00406051	intron-variant	RFWD3	GRCh38.p7	16:74649247	GAGGTAAAATACAAA[A/G]TAAGATATGTCAGGT	55159
rs745508914	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74650568	CCCTGCAACCTAATG[A/G]TTTTAGGATCCACTG	55159
rs745511636	snp	C/G	1.85166e-05	0.00304269	intron-variant	RFWD3	GRCh38.p7	16:74624085	AGCTAAAGAACACAA[C/G]CAGAGGGAAGGGTCA	55159
rs745588513	snp	A/C	1.6708e-05	0.00289028	missense	RFWD3	GRCh38.p7	16:74661401	CTGGCTGTTGTTCGG[A/C]ATGATTTAACTGCAC	55159
rs745588549	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74665353	GCACTTTGGGAAGCC[A/G]AGGGCAGACCACTTG	55159
rs745673822	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74633278	CAAAACTCCGTCTCA[-/G]GAAAAAAAAAAAAAA	55159
rs745712842	snp	A/G	7.03309e-05	0.00592963	intron-variant	RFWD3	GRCh38.p7	16:74626568	ATCTATGGGACAGAG[A/G]AATCAGTGCTGCACC	55159
rs745769790	snp	A/G	1.64735e-05	0.00286993	intron-variant	RFWD3	GRCh38.p7	16:74644332	GAACCAAAAGGGAAC[A/G]TTCCAGCCAGGCATA	55159
rs745874781	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650650	TTTCTATCGTTCCTG[C/T]TGCAATTAGCTGAAA	55159
rs745960311	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74655266	TTTTTTTGAGACAGA[-/G]TCTCACTTTGTCGCC	55159
rs745963475	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74643380	CTGTTCATGCATACA[C/G]CACCGTTCATTCAAC	55159
rs745970908	snp	C/G	1.67452e-05	0.0028935	missense, intron-variant	RFWD3	GRCh38.p7	16:74630793	TACCTGGCTTTCTGA[C/G]CTACTAACTCCTGCA	55159
rs746048092	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74627053	AATAGGACCCCCAGG[A/C]TTTGTACACCAGTCA	55159
rs746134638	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627890	AAACCTAGAACACTG[A/G]CCATCAGTACAGTTT	55159
rs746141566	snp	A/G	1.64741e-05	0.00286998	missense	RFWD3	GRCh38.p7	16:74644575	TGTCCTTTAAGCCAC[A/G]TGGAAATGCACCTAT	55159
rs746152970	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RFWD3	GRCh38.p7	16:74661228	GTCAACAGACAGTTG[C/T]GGAGCAGGCTGGAGC	55159
rs746182799	snp	A/G	1.64757e-05	0.00287012	missense	RFWD3	GRCh38.p7	16:74651949	GCTCCAGATTCCTCT[A/G]CCTGGTCAACAACCC	55159
rs746186531	snp	C/T	1.64741e-05	0.00286998	missense	RFWD3	GRCh38.p7	16:74636486	TGCTTGTGCTGGCCC[C/T]GGCTGGAGGGTGAGC	55159
rs746220972	snp	C/G	2.34563e-05	0.00342456	intron-variant	RFWD3	GRCh38.p7	16:74624123	GTCAGTACACGAAGG[C/G]ACTTCCATTCTTCAT	55159
rs746259338	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660367	CTGAGGCAGGAGAAT[C/T]GCTTGAATCTGGGAG	55159
rs746369353	snp	C/T	1.66344e-05	0.0028839	intron-variant	RFWD3	GRCh38.p7	16:74628693	GTAAGGAAACTGTAT[C/T]TCACACTCCAAAACT	55159
rs746377038	snp	A/G	2.12177e-05	0.00325705	intron-variant	RFWD3	GRCh38.p7	16:74636588	AAGTCCTAAAATGAA[A/G]AAGATTTTATAAATA	55159
rs746436198	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74628370	TACCACAGCCACCCA[-/C]AAGGGTAGGATCAAA	55159
rs746442923	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623442	CTACAGTGCCCTCTT[C/G]TGTTCAACTGAATAA	55159
rs746444144	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74645842	ACTGCAAGTTCCGCC[G/T]CCTGGGTTCACACCA	55159
rs746470985	in-del	-/CAAC	3.31549e-05	0.0040714	intron-variant	RFWD3	GRCh38.p7	16:74632476	GAATTCCATGCTACT[-/CAAC]CAACACCAAAGAGCC	55159
rs746505214	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74665751	TTTCTTTCTTTCTTT[-/C]CTTTCTTTTTTTGAG	55159
rs746525574	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74647709	CGATTCTCCTATCTC[A/T]GCCTCCTGAGTAGCT	55159
rs746526115	snp	C/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621271	TACAGAGCAAGATTC[C/T]GTCTCAAAAAACAAA	55159
rs746529602	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657973	CCAGTAAAAAAGTGA[C/T]AGACGATTAAAAAAA	55159
rs746617393	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74666135	ATTAAATCCCTGTTC[C/T]TTTACTACATGGGGA	55159
rs746627849	snp	A/G	1.66815e-05	0.00288799	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630957	GGTATTTGTCTCCAG[A/G]CTGTGGAGTTACAAA	55159
rs746638994	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74640726	GAGTGGATCACGAGG[C/T]CAGGAGTTCAAGACC	55159
rs746665967	snp	A/G	1.64741e-05	0.00286998	intron-variant	RFWD3	GRCh38.p7	16:74644312	TTTTCAGATGTGCCT[A/G]CAATGAACCAAAAGG	55159
rs746677609	snp	A/C/G	3.29469e-05	0.00405864	missense, intron-variant	RFWD3	GRCh38.p7	16:74630894	AGCCTCATCAAGACA[A/C/G]CAGCAACAGCTCCAG	55159
rs746815538	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637009	TGAGCCACCGCGCCC[A/G]GCCAGAACTGCTGAG	55159
rs746915233	snp	A/C	1.68513e-05	0.00290265	intron-variant	RFWD3	GRCh38.p7	16:74652130	CTCTCAACCTATGTA[A/C]ACAGAAAGACAACGG	55159
rs746929131	snp	A/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662818	TTGTGGGAGTCCAGA[A/C]CAGAGGTCAGAGAGA	55159
rs746935093	snp	A/G	1.65897e-05	0.00288003	stop-gained	RFWD3	GRCh38.p7	16:74626534	CCATCAGCACACTTC[A/G]TATGGTGGTGTGATT	55159
rs746955316	snp	A/C/T	3.29469e-05	0.00405864	missense	RFWD3	GRCh38.p7	16:74626461	CCTCCAAAAAATGTA[A/C/T]GTACAGGCTGGCAGG	55159
rs747018311	snp	A/G	1.68464e-05	0.00290222	missense	RFWD3	GRCh38.p7	16:74636561	TGACTTTGATGTGAC[A/G]TAAGTTTTTGCAAGT	55159
rs747034080	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74647606	ATTATTATTACTATT[C/G]TTTGAGATGAAGTCG	55159
rs747052087	snp	A/G	6.59304e-05	0.00574116	missense	RFWD3	GRCh38.p7	16:74628547	ACATGAGGCCAATGA[A/G]AAAAGTCCATTTTCT	55159
rs747144308	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622734	CTTGAAGCATATTCT[A/G]TTGTGGAAGTGGGTT	55159
rs747145923	in-del	-/ATAG	2.17578e-05	0.00329825	intron-variant	RFWD3	GRCh38.p7	16:74649101	TAAATAAATAAATAA[-/ATAG]ATTTTTTTAAAATGA	55159
rs747206941	snp	G/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644446	CTGTGCCTGGCTTTC[G/T]TGTTGCACTAAAGAA	55159
rs747210793	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74643512	ATTACTAGATCAAAG[C/G]CTTTAGAGACACATT	55159
rs747245848	snp	A/G	1.66051e-05	0.00288137	intron-variant	RFWD3	GRCh38.p7	16:74628683	TGAAAGGAAAGTAAG[A/G]AAACTGTATCTCACA	55159
rs747255492	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RFWD3	GRCh38.p7	16:74661006	CCTTCTTGTTCTCAT[C/T]GGCCCTACACTGTGG	55159
rs747299187	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640169	TTTTTTTTTGAAACA[A/G]TCTTGCTCTGTTGCC	55159
rs747307227	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74650804	ATCGCTTGAGCCTGG[A/G]AGGTCAAGGCTGCGG	55159
rs747353198	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639373	TACAACATCACTTAC[A/G]CAACAGAATTTTCAG	55159
rs747371853	snp	A/T	3.30453e-05	0.00406467	missense	RFWD3	GRCh38.p7	16:74624008	CCTCAAATGGGCAGA[A/T]GTCCAACACAGGCTG	55159
rs747376784	in-del	-/TA			intron-variant	RFWD3	GRCh38.p7	16:74634381	TTACTAAGTACTTTA[-/TA]TATATATATATATAT	55159
rs747378714	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658916	GGGACCACAGGTGTG[C/T]GCCACCACGCCCGGC	55159
rs747395160	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74651861	TAGTTTCTAGCCTTC[C/T]GAAATTTAAGCTTCA	55159
rs747413031	snp	C/G	3.31296e-05	0.00406985	missense	RFWD3	GRCh38.p7	16:74661339	ATCAGCAGGAACAGG[C/G]TGGAGGAGGGCTGGT	55159
rs747499976	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660506	AGGCAATTGTTATTC[C/T]TCATAATAACCCTGT	55159
rs747515646	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74624345	TGCCAGCCTCTTCTA[C/G]GGACAGAAGGGTCAA	55159
rs747523004	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624811	GACCAGCTGGGGCAA[C/T]ACAGCAAGAATCCAA	55159
rs747530329	snp	C/G	1.64738e-05	0.00286995	missense	RFWD3	GRCh38.p7	16:74636470	TTGGAAGTGGTACTT[C/G]TGCTTGTGCTGGCCC	55159
rs747571282	snp	A/G	1.77209e-05	0.0029766	synonymous-codon	RFWD3	GRCh38.p7	16:74624071	TGGCAGCATCCCACA[A/G]CTAAAGAACACAAGC	55159
rs747582055	snp	A/G			missense	RFWD3	GRCh38.p7	16:74661443	ATTCCATTGCTTCAT[A/G]AGCCATCACTAGAGA	55159
rs747608873	snp	A/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623156	AAGCTGGCTAGAAAA[A/C]ACAAAATCTTCCCCA	55159
rs747631399	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74630655	CTGAAGTGAGATCAA[C/G]TGGATCTTCAAAAAA	55159
rs747635398	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74647669	CTATTTGGGCTCACT[C/G]CAACTTCTGCCTCCC	55159
rs747674672	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668216	AACGAATCCTTAATT[G/T]TCAATAGGGTGACTG	55159
rs747676226	in-del	-/TAG			intron-variant	RFWD3	GRCh38.p7	16:74666195	GATTAGATAGATAGA[-/TAG]ATAGATAGATAGATA	55159
rs747737249	snp	C/G	1.92866e-05	0.00310531	missense	RFWD3	GRCh38.p7	16:74637954	GTTTCCTTAGCATCT[C/G]TTCCTTCAGTAGGGA	55159
rs747788655	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74658130	AACCCAAGAAATTCT[A/C]CTCCTTCCCTGCACT	55159
rs747865334	snp	C/T	1.66335e-05	0.00288383	synonymous-codon	RFWD3	GRCh38.p7	16:74652116	AGCATCCAATGGTGC[C/T]CTCAACCTATGTACA	55159
rs747901662	snp	A/C/T	1.69364e-05	0.00290997	missense	RFWD3	GRCh38.p7	16:74637888	GCCTAGTGCACTTAT[A/C/T]AGTGAGGACCTGCAG	55159
rs747905365	snp	C/G	3.29473e-05	0.00405864	missense	RFWD3	GRCh38.p7	16:74644561	GACATTTTCGTACTT[C/G]TCCTTTAAGCCACGT	55159
rs747943641	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628069	AGCCGGGCTACTACA[C/T]GGCTGCCCTAATCTG	55159
rs748004464	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74654430	GTGCAAGAATCACAC[A/C]CATATAAGATGGTGA	55159
rs748024154	in-del	-/CTTCC	1.65703e-05	0.00287834	intron-variant	RFWD3	GRCh38.p7	16:74632481	CCATGCTACTCAACA[-/CTTCC]CCAAAGAGCCCAGTC	55159
rs748040145	in-del	-/A	3.35892e-05	0.00409798	intron-variant	RFWD3	GRCh38.p7	16:74644743	GAGATGGCTAGATGG[-/A]AAAGCAGAATATATT	55159
rs748083506	snp	A/G	1.70983e-05	0.00292384	intron-variant	RFWD3	GRCh38.p7	16:74632683	CAAAGCCTGAAAAAG[A/G]CAAAATAGTATGAAA	55159
rs748102081	snp	A/T	3.29647e-05	0.00405971	missense	RFWD3	GRCh38.p7	16:74632613	CGGATCTGTTTGCCA[A/T]GCATCGGAATGTACT	55159
rs748118061	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74660643	GGTGAGTAGAGACTT[G/T]CAAGTGAAGAAAGAA	55159
rs748145728	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627225	ATTTAATGACTAACT[C/T]TGACTATACATCTGC	55159
rs748157441	in-del	-/TATA			intron-variant	RFWD3	GRCh38.p7	16:74634379	TTTTACTAAGTACTT[-/TATA]TATATATATATATAT	55159
rs748180724	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RFWD3	GRCh38.p7	16:74636397	TCACCAGGCAGCTCA[A/G]AGCATCACAGTATGC	55159
rs748241016	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74652398	TCTGGCCATATTGTC[A/G]GTATCTTTAAAGGAC	55159
rs748358449	snp	A/C	1.64825e-05	0.00287071	synonymous-codon	RFWD3	GRCh38.p7	16:74628528	CCCTGGCTCCAAGGG[A/C]AGCACATGAGGCCAA	55159
rs748374779	snp	A/G	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74636460	TGAAGGTCTTTTGGA[A/G]GTGGTACTTGTGCTT	55159
rs748377043	snp	A/G	1.88039e-05	0.0030662	intron-variant	RFWD3	GRCh38.p7	16:74626586	TCAGTGCTGCACCAT[A/G]GGGACGCTACACAAA	55159
rs748422189	snp	A/G	3.29468e-05	0.00405861	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630876	TCCAGCATAGATGTA[A/G]TTAGCCTCATCAAGA	55159
rs748526156	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74642045	CAAATACATAATAAC[A/T]CTTGGGAATGCTGAA	55159
rs748617245	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625583	TTTTTTCTTCTGCCA[C/T]TGACTTGTTGTGGAA	55159
rs748632380	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74652132	CTCAACCTATGTACA[C/G]AGAAAGACAACGGAA	55159
rs748644319	in-del	-/TTTT			intron-variant	RFWD3	GRCh38.p7	16:74657473	ATCACCCAGGTTTTC[-/TTTT]TCTTTTTTTTTTTTT	55159
rs748658412	snp	C/T	1.65787e-05	0.00287907	intron-variant	RFWD3	GRCh38.p7	16:74649120	ATTTTTTTAAAATGA[C/T]GTTCATATTACCTGT	55159
rs748660247	snp	C/G	1.64966e-05	0.00287194	missense	RFWD3	GRCh38.p7	16:74623994	GCTGTTACGGTTCAC[C/G]TCAAATGGGCAGATG	55159
rs748667768	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74659008	AAAGGGATCCGCCTG[-/C]CTTGGCCGCTCAAAG	55159
rs748680308	snp	G/T	3.32718e-05	0.00407858	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623903	ATCTAACCAGCAGCA[G/T]GCCTTCAAGGTTTCG	55159
rs748724357	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74640940	CGAGACTCTGTCTCA[A/C]AATAAATAAAATTCA	55159
rs748748644	snp	C/G	1.65345e-05	0.00287524	missense	RFWD3	GRCh38.p7	16:74661323	CCTGGCTGCTGACCA[C/G]ATCAGCAGGAACAGG	55159
rs748774970	snp	C/T	1.89593e-05	0.00307885	intron-variant	RFWD3	GRCh38.p7	16:74661501	AATAGATAAAACATG[C/T]TATGTAGGTGACAGA	55159
rs748795600	snp	A/G	3.29565e-05	0.00405921	missense	RFWD3	GRCh38.p7	16:74632599	TAAACGCCAGTCCAC[A/G]GATCTGTTTGCCATG	55159
rs748861914	snp	C/G	1.64784e-05	0.00287035	missense	RFWD3	GRCh38.p7	16:74652017	ACTACTAGACACCTG[C/G]AACTCTTCAGATACA	55159
rs748899994	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623250	TTAGCAAAGGGAATC[A/G]TTCACTAGCTGCTTC	55159
rs748916677	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632949	TGGGATTACAGGCAT[A/G]AGCCACCACACCTGG	55159
rs748923851	snp	C/T	2.46278e-05	0.00350903	intron-variant	RFWD3	GRCh38.p7	16:74636598	ATGAAAAAGATTTTA[C/T]AAATACAAAGCTTTT	55159
rs748950889	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659622	AAAAACCCAGAGTAA[C/T]ATGCATTTGCAACTC	55159
rs748953046	in-del	-/TAGA			intron-variant	RFWD3	GRCh38.p7	16:74666182	ATTAGATAGACAGAT[-/TAGA]TAGATAGATAGATAG	55159
rs748985693	snp	C/G	3.30006e-05	0.00406192	intron-variant	RFWD3	GRCh38.p7	16:74626322	ACTTTTTATATGAAA[C/G]TAAAAAAGTAACAGG	55159
rs748988162	snp	A/C	1.64825e-05	0.00287071	missense	RFWD3	GRCh38.p7	16:74623972	TCTCTGTTAAGGTAG[A/C]CAAGTAGCTGTTACG	55159
rs749019766	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648813	TATTCAGGTTGGGCA[C/T]GGTGGCTCATGACTA	55159
rs749041723	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74637118	GGTTTCGTTTAAAGT[A/C]CTTTAAAAAAAAAAA	55159
rs749055241	snp	A/G	1.64732e-05	0.0028699	intron-variant	RFWD3	GRCh38.p7	16:74644342	GGAACATTCCAGCCA[A/G]GCATACTCTTACCAC	55159
rs749086452	in-del	-/AAAT	0.000534045	0.0163321	intron-variant	RFWD3	GRCh38.p7	16:74649082	AGACCTAGTCTCTAA[-/AAAT]AAATAAATAAATAAA	55159
rs749093180	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74650168	CTGATTTGAGATATT[A/C]CCTTCACAATATGTT	55159
rs749093344	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74665259	CCAGACCAGCTTGGG[A/C]AACACAGTGAAATTC	55159
rs749101844	in-del	-/AG	1.64743e-05	0.00287	frameshift-variant	RFWD3	GRCh38.p7	16:74661219	TTCTGTCAGGTCAAC[-/AG]ACAGTTGCGGAGCAG	55159
rs749105843	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656620	GCACACCATGCCCAG[C/T]TAATTTTTGTATTTT	55159
rs749127097	snp	C/T	0.000267939	0.0115714	missense	RFWD3	GRCh38.p7	16:74660939	TTATTTACCTGGCAC[C/T]GTCTGTCCTCTGAGA	55159
rs749131662	snp	A/G	0.000197655	0.00993922	synonymous-codon	RFWD3	GRCh38.p7	16:74644421	TCGGGCATAAAGGAC[A/G]ACAATGTCACTGTGC	55159
rs749142702	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628364	TGAGCGGTACCACAG[C/T]CACCCAAAGGGTAGG	55159
rs749199989	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74638887	TACAGAAACCTACAC[A/G]GTATAGCCTACTACA	55159
rs749289346	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74665935	ACTCCTGGCCTCAGG[A/T]GATCCGACTGCCTCG	55159
rs749290544	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74666408	AAGTGATGAAGTAAT[-/C]GGCGCTCAGAGCGGG	55159
rs749298525	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629245	GAAGTCGTTCGTGCC[A/G]AAGTTGCCAAAGTGT	55159
rs749315983	snp	C/T	1.65833e-05	0.00287948	missense	RFWD3	GRCh38.p7	16:74644717	AAGGTAGCAGAGGCT[C/T]AGACTTCTGGGGAGA	55159
rs749389485	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74626673	ATAAATGCATTAAAC[A/C]ATCAAGAACAGTTAC	55159
rs749412303	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653156	CCAGCCTGATTAACA[C/T]GGTGAAACCCCATCT	55159
rs749426850	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654582	ACTCTACAATGGCCT[C/T]TAAGTGTTCAAATTA	55159
rs749453678	snp	C/G	1.64746e-05	0.00287002	missense	RFWD3	GRCh38.p7	16:74626469	AAATGTATGTACAGG[C/G]TGGCAGGAGCAGATT	55159
rs749510295	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	RFWD3	GRCh38.p7	16:74636389	CTGTGATATCACCAG[A/G]CAGCTCAGAGCATCA	55159
rs749547685	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625486	GCCTCTGCACTCCAG[C/T]CTGGGTAACAGAGCG	55159
rs749665162	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632264	AGGCATGGTTGCAGG[C/T]GCCTGTAGTCCTAGC	55159
rs749682877	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74624303	TAAGTGGACCTGAAA[A/T]AAAGCCCAGCTTCCA	55159
rs749763107	snp	A/G/T	6.58962e-05	0.00573974	missense	RFWD3	GRCh38.p7	16:74661242	GCGGAGCAGGCTGGA[A/G/T]CAGGGGTGGTGTCGC	55159
rs749774971	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642226	CTCCCAGGTTCAAGC[A/G]ATTCTCGTGCCTCAG	55159
rs749804490	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant	RFWD3	GRCh38.p7	16:74630865	CCATTGGCCAGTCCA[A/G]CATAGATGTAGTTAG	55159
rs749815578	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668283	CTGAATTCTCAGACA[C/T]ACCCAGAAGAACACC	55159
rs749859557	snp	G/T	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661087	TCCGCTGATGAAGTT[G/T]GTCATTGAATGCAAC	55159
rs749871029	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662235	CTCATGCATCAGGAC[A/T]ACAGGACTGAGCCAC	55159
rs749880043	in-del	-/TTCTT			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662071	TATTAAGCACCTATG[-/TTCTT]TTCATGTTTCCTATC	55159
rs749951263	snp	C/T	1.68849e-05	0.00290554	intron-variant	RFWD3	GRCh38.p7	16:74628716	CCAAAACTCGGACGG[C/T]TCCAGACCCCACTAC	55159
rs749972718	in-del	-/AAAA			intron-variant	RFWD3	GRCh38.p7	16:74638370	AAAGAATCTGAAGTT[-/AAAA]AGAGCAAAAGTAGAC	55159
rs749992129	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74635505	AGGTAACAGAAATAC[A/T]CACCGAGTTAATCAT	55159
rs750040144	snp	A/C/T			intron-variant	RFWD3	GRCh38.p7	16:74624748	CACCTGTAATTCCAA[A/C/T]ACTTTGGGAGTCTGA	55159
rs750049616	snp	C/T	1.64738e-05	0.00286995	intron-variant	RFWD3	GRCh38.p7	16:74644538	CTTACCTATGGTCCT[C/T]ACCTGGGGACATTTT	55159
rs750061578	in-del	-/AT	1.64901e-05	0.00287137	frameshift-variant, intron-variant	RFWD3	GRCh38.p7	16:74630834	CGTGTTTCGCACGTC[-/AT]ATACCAGAATTGAAC	55159
rs750065808	snp	C/G	1.64765e-05	0.00287019	missense	RFWD3	GRCh38.p7	16:74632580	AAGCCTCTGAGGTAA[C/G]TGCTAAACGCCAGTC	55159
rs750083029	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74657439	TCTCTGTGGTCCTTA[A/C]TCTGCCATTTTCACT	55159
rs750106194	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74651601	CTCCAGTTGTCACTG[G/T]GGGACAGAGCCAGAC	55159
rs750147212	snp	C/G/T	8.23613e-05	0.00641675	synonymous-codon, missense	RFWD3	GRCh38.p7	16:74636452	AGATACTGTGAAGGT[C/G/T]TTTTGGAAGTGGTAC	55159
rs750180032	snp	C/G	1.66158e-05	0.0028823	intron-variant	RFWD3	GRCh38.p7	16:74651891	ATGGATGTTAGCCTT[C/G]TGAGTCCAAACCTGG	55159
rs750220423	in-del	-/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623038	TGATCTCTGACACTA[-/G]GGGGAGACTCAAGTA	55159
rs750237509	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74658514	GTAAATGTCAAACAC[C/G]ACACTGAGAAATTCA	55159
rs750396562	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667951	AAACAGGGGAGTAAA[A/G]ACTCCAGTAACCCTC	55159
rs750404391	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74641046	AATATTTAGGTAAAG[A/C]TGAAATTAAATGTGC	55159
rs750430318	snp	C/G	3.3151e-05	0.00407117	missense, intron-variant	RFWD3	GRCh38.p7	16:74630809	CTACTAACTCCTGCA[C/G]ATGACTGCTCGTGTT	55159
rs750500794	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628977	TGAAGCTTCTGGAAA[C/T]GGGTTTAGCCACATA	55159
rs750533449	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659691	GCACTACAGACACTG[A/G]AGCCACAGTCATGGC	55159
rs750557933	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668407	GCAACTACACCAACA[A/G]GAATTAGTGCTAGTT	55159
rs750587176	snp	A/C	1.67013e-05	0.0028897	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623884	CTAGGCGCTAGCAAA[A/C]AACATCTAACCAGCA	55159
rs750590044	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74665572	AACAAAGCGAGACTC[C/T]ATCTCAAAAAAAGAA	55159
rs750608635	snp	A/C	3.30262e-05	0.0040635	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630930	ACGTCCAGCATTATA[A/C]GTCTGGACCACGGTA	55159
rs750619812	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74649875	CTAATGAAATGTCCT[A/G]CACATCCTGGATTTG	55159
rs750673352	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74631972	ATATACTTAAGACAT[-/A]TTTTGTAATATACAT	55159
rs750696196	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74638576	TCCAGTAAGATATGC[A/G]AGAAAAAGATGAAAA	55159
rs750725702	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74664997	ACCTTGAGGATGTCA[C/T]ACAAACGCTGTTTTT	55159
rs750762455	in-del	-/ATC	5.08699e-05	0.00504305	cds-indel	RFWD3	GRCh38.p7	16:74637886	AAGCCTAGTGCACTT[-/ATC]AGTGAGGACCTGCAG	55159
rs750801330	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74634732	TCCTAGATTCAAGAT[A/T]GCTTCAGCTTCTCCA	55159
rs750820411	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645991	CTGACCTCGCGATCC[A/G]TCCGCCTTGGCCTCC	55159
rs750829372	snp	C/T	1.65395e-05	0.00287567	missense	RFWD3	GRCh38.p7	16:74632647	TGCTCTTCATGTTGG[C/T]AGTACTCAACATCTT	55159
rs750831194	snp	C/T	1.65285e-05	0.00287471	intron-variant	RFWD3	GRCh38.p7	16:74626315	CAAAACTACTTTTTA[C/T]ATGAAAGTAAAAAAG	55159
rs750874215	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74629610	CCAGCCTGGGTGACA[C/G]AGTGAGACACCATCT	55159
rs750912573	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74656201	TACTCTGTAGGCTGA[G/T]GCAGGAGGATCGAGG	55159
rs750926967	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656393	GCTTTTTTTATTTTA[C/T]TTTTTTTAATTTCTT	55159
rs750944744	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74647489	GATGGGGTTTCACCC[G/T]GTTGGCCAGGCTGGT	55159
rs750952709	snp	C/T	1.65228e-05	0.00287422	synonymous-codon	RFWD3	GRCh38.p7	16:74652089	AGGCTGGGTCCTGCT[C/T]ACCTGAAAGTAAGCA	55159
rs750953750	snp	G/T	1.64727e-05	0.00286986	missense	RFWD3	GRCh38.p7	16:74626425	AAAATGGCATTTTTG[G/T]TCAATAGTTTGCAAG	55159
rs750996648	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74665756	TTTCTTTCTTTCTTT[-/C]TTTTTTTGAGATGGA	55159
rs751019069	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74649675	TAAATATCCAGGCAT[C/G]CAGTTCATATTCAAA	55159
rs751110014	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667656	AGACAAGATGATAAA[G/T]ACGATCTAGATGTAA	55159
rs751116617	snp	G/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621891	TAGTAGAGATGGGGT[G/T]TCACCATGTTGGTCA	55159
rs751156403	in-del	-/A	1.64754e-05	0.00287009	intron-variant	RFWD3	GRCh38.p7	16:74644322	TGCCTACAATGAACC[-/A]AAAGGGAACATTCCA	55159
rs751183276	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74653013	TACTAAAAACCAGGA[A/G]TTCCTGAGGAAGGAT	55159
rs751195667	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644396	CACTAGTGTCCAAAG[C/T]TCTCAGGGTTCGGGC	55159
rs751201026	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74626283	AAGTTCATGTTTTCC[C/T]TTACCAATATTTTAA	55159
rs751208479	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661071	CATGAAGTCTCTGCA[A/G]TCCGCTGATGAAGTT	55159
rs751238014	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74644010	TTCCGAAATCCTGGT[-/A]ATTTTTTACATTGCA	55159
rs751239938	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74640799	AAAAAATTAGCCAGG[C/T]GTGGTGGCGGGTGCC	55159
rs751244217	in-del	-/G	4.94809e-05	0.00497373	frameshift-variant	RFWD3	GRCh38.p7	16:74652059	CTCTGAATCATAAGT[-/G]GTAGCTGGCAAGTCA	55159
rs751271171	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74653636	TAGCCAACAAAGTAA[C/G]ACACCATCTCTATTA	55159
rs751314153	snp	C/T	1.66291e-05	0.00288345	missense	RFWD3	GRCh38.p7	16:74661359	GGAGGGCTGGTCCCC[C/T]TTGGCTGCTGGCCAT	55159
rs751320642	snp	C/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668122	AAGCAAAAGGGTGCA[C/G]GCTTCAGAATATTTT	55159
rs751323470	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648708	ACACGGGAGGCAGAG[A/G]TTATTGTGGTGAGCT	55159
rs751389192	snp	A/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623691	AATGAAGGCTTTAAA[A/C]CCAAGAAATGGATAA	55159
rs751423797	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668479	CTCAGTGATTTGAGG[A/G]TGGAGGAGTCGTTTT	55159
rs751460444	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636340	CTGAGGTTCTAGACT[C/T]TTTACCTGGAAGAAA	55159
rs751467896	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74631986	TATTTTGTAATATAC[A/T]TAGTTTCAAAGAAAC	55159
rs751490655	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74658556	TCAGAAGTTATAAGC[A/G]ATTAGTCCTGGGAAA	55159
rs751495160	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632887	AACCTCAGCTCACTA[C/T]AACTTCTGCCTCCCG	55159
rs751506927	snp	A/C/T	3.29453e-05	0.00405854	synonymous-codon, missense	RFWD3	GRCh38.p7	16:74636434	CCGGCAGTTTCCTGC[A/C/T]TGAGATACTGTGAAG	55159
rs751507735	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655662	TCTCGCTCTGTCACC[C/T]AGGCTGCAGTGCAGT	55159
rs751517534	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74659415	ACCCTGCCTTTATAA[A/C]GTGAGTAATGACATC	55159
rs751527081	snp	C/T	1.6476e-05	0.00287014	missense	RFWD3	GRCh38.p7	16:74649161	TCTTGCCTCCATCGA[C/T]ACATGTAACTTCTTG	55159
rs751540083	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623875	TTGGGGCTGCTAGGC[A/G]CTAGCAAACAACATC	55159
rs751576176	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74624345	TGCCAGCCTCTTCTA[-/G]GGACAGAAGGGTCAA	55159
rs751595216	in-del	-/TAGATAG			intron-variant	RFWD3	GRCh38.p7	16:74666195	GATTAGATAGATAGA[-/TAGATAG]ATAGATAGATAGATA	55159
rs751609817	in-del	-/A			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664082	AAATAAGTGGGAAAG[-/A]AAGTCTGCAAACTGA	55159
rs751615664	snp	C/T	9.88549e-05	0.00702977	missense	RFWD3	GRCh38.p7	16:74652007	CAGAATCAGAACTAC[C/T]AGACACCTGCAACTC	55159
rs751685397	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629110	ATTTTAATTCAGAAA[C/T]AGGACTGTTTTAGGT	55159
rs751713966	snp	G/T	1.64727e-05	0.00286986	synonymous-codon	RFWD3	GRCh38.p7	16:74626388	ACACACCAGGATGTT[G/T]CCATCATTCTCTGGG	55159
rs751726445	snp	C/T	1.70365e-05	0.00291855	missense	RFWD3	GRCh38.p7	16:74637917	AGTTGGAGTCGGCAC[C/T]GTGCTGATTCTAACT	55159
rs751746070	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74661865	GCAATATTAATCTTT[C/T]ACAGCATCAACAGTT	55159
rs751776382	snp	C/T	1.72124e-05	0.00293359	intron-variant	RFWD3	GRCh38.p7	16:74630773	GAAAAGAGTGAGTGG[C/T]TCCCTACCTGGCTTT	55159
rs751816148	snp	A/C	1.77593e-05	0.00297982	synonymous-codon	RFWD3	GRCh38.p7	16:74637859	GGACAAACGTACCTG[A/C]ACACGCCTTTGAAGC	55159
rs751877082	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74656474	GAAAACCTTGAAATG[A/T]TCCACCATTCTTTTT	55159
rs751941595	snp	A/G	1.65496e-05	0.00287655	intron-variant	RFWD3	GRCh38.p7	16:74626299	TTACCAATATTTTAA[A/G]CAAAACTACTTTTTA	55159
rs751950900	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625406	GTGCACCCAGCTACT[C/T]GGGAAGCTGAGGCAC	55159
rs751960464	snp	C/G	1.65825e-05	0.00287941	intron-variant	RFWD3	GRCh38.p7	16:74632483	CATGCTACTCAACAC[C/G]AAAGAGCCCAGTCTC	55159
rs751984728	snp	A/T	1.65143e-05	0.00287348	intron-variant	RFWD3	GRCh38.p7	16:74651912	CCAAACCTGGGTAAA[A/T]TACTGACCTTCTAAA	55159
rs751995562	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621643	TAAAGCCTGGATTTA[C/T]AAATGTGATGTCCTA	55159
rs752013356	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74632257	ATTAGCCAGGCATGG[G/T]TGCAGGCGCCTGTAG	55159
rs752038940	snp	A/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662263	CACTGTGCCTCCCTA[A/C]CACCTAGTTTTTAAA	55159
rs752073753	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74646159	GCAGGAGGATTCCTT[C/G]AGCTCAGGAGTTTGA	55159
rs752079432	snp	C/T	1.64817e-05	0.00287064	missense	RFWD3	GRCh38.p7	16:74632542	TCAGTTTAATAGTGT[C/T]GTCTAGGGAAGCAGA	55159
rs752147094	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74653362	AACAAAAAAATGACA[C/G]CCAAAAAACTTGGGA	55159
rs752165875	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635579	GACTGGAATGGACAC[A/G]TTAAGAAAAAAAGAA	55159
rs752181138	snp	C/T			synonymous-codon	RFWD3	GRCh38.p7	16:74632528	AATCACTCACCTGGT[C/T]AGTTTAATAGTGTTG	55159
rs752201775	in-del	-/GAA	4.94173e-05	0.00497053	cds-indel	RFWD3	GRCh38.p7	16:74661031	CTGTGGTTTGAAGAT[-/GAA]GGTCTCAGGAATTCC	55159
rs752202050	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74633094	CAAGCCTGGCCAACA[C/G]AGTGAAACCCTGTCT	55159
rs752310642	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74642904	TTTTGAAACTCTTCA[C/G]TTTTTCTAATGAGGC	55159
rs752326359	snp	C/T	3.3222e-05	0.00407553	intron-variant	RFWD3	GRCh38.p7	16:74628439	AGCTATGGGAGACCC[C/T]AGCACTACTTACCAG	55159
rs752328930	snp	A/C/G	0.000124149	0.00787783	intron-variant	RFWD3	GRCh38.p7	16:74660897	ATAATTTCTAGTACA[A/C/G]CAATGATCACAGACT	55159
rs752389383	snp	A/C	1.64738e-05	0.00286995	missense	RFWD3	GRCh38.p7	16:74661215	CCACTTCTGTCAGGT[A/C]AACAGACAGTTGCGG	55159
rs752398601	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643968	AGGCGTGAGCCACCA[C/T]GCCCGGCCCTAGCAA	55159
rs752444280	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638815	TTAATGATGTGGGCA[C/T]GTTCTGAGAAACATG	55159
rs752470600	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74651445	AACATGGAAAAACTC[-/T]TGTCTCTACAAAAAA	55159
rs752480625	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74628370	GTACCACAGCCACCC[A/C]AAGGGTAGGATCAAA	55159
rs752481084	snp	C/T	1.6489e-05	0.00287128	missense, intron-variant	RFWD3	GRCh38.p7	16:74630835	GTGTTTCGCACGTCA[C/T]ATACCAGAATTGAAC	55159
rs752482587	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622185	TCTGCTGAAGCCAGA[C/T]GAGTTCTGCTTTTTA	55159
rs752568814	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640867	TCACTTAAACCCGGG[A/G]GGTGGAGGTTGTAGT	55159
rs752636751	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658046	AGTCAGGCAAGAACA[C/T]AGGAAAGGGGAACTG	55159
rs752666614	snp	C/T	3.44917e-05	0.00415267	intron-variant	RFWD3	GRCh38.p7	16:74644773	TCAAATTAGAGAAAA[C/T]GTAAAATCAATCTTG	55159
rs752680285	snp	A/G	1.64996e-05	0.0028722	synonymous-codon	RFWD3	GRCh38.p7	16:74661294	AGGAGCTGGCTGGAG[A/G]ATGGATGGTACCCCC	55159
rs752726742	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647356	GCAATGGCACAATCT[C/T]GGCTCACCACAACCT	55159
rs752731902	in-del	-/T	3.32419e-05	0.00407675	intron-variant	RFWD3	GRCh38.p7	16:74628689	AAAGTAAGGAAACTG[-/T]TATCTCACACTCCAA	55159
rs752748829	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646459	CAACACAGGCGTGTG[C/T]CACCATACACCAACC	55159
rs752748854	in-del	-/GTCCGCCTC			intron-variant	RFWD3	GRCh38.p7	16:74630341	CTGACCTCCTGATCT[-/GTCCGCCTC]GTCTTCCCAAAGTGC	55159
rs752776205	snp	C/T	1.78717e-05	0.00298923	intron-variant	RFWD3	GRCh38.p7	16:74661464	TCACTAGAGAAACAG[C/T]ATTTGTAAAAAGTAT	55159
rs752803087	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74625227	AAGTAGAGAGGGACA[C/G]AAAAAAAAAGGTAGA	55159
rs752834631	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74665091	TTCAATCAATGGCCA[C/T]AACAGGCAGGACGAA	55159
rs752851682	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74657476	CCCAGGTTTTCTTTT[-/TT]TCTTTTTTTTTTTTT	55159
rs752853275	snp	C/G	1.64743e-05	0.00287	missense	RFWD3	GRCh38.p7	16:74651981	TCCATACTCTGCAGA[C/G]CTGTCACTGTCAGAA	55159
rs752856160	in-del	-/TG			intron-variant	RFWD3	GRCh38.p7	16:74666215	GATAGATAGATAGAT[-/TG]AGATAGATTGATTAG	55159
rs752888882	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657701	CTGGTCTCGAACTCG[C/T]GACCTCAGGTGATTC	55159
rs752937810	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645556	GTGGGTTTCACCATG[C/T]TGGCCGGGCTGGTCC	55159
rs752972452	snp	A/C	1.65693e-05	0.00287826	intron-variant	RFWD3	GRCh38.p7	16:74651902	CCTTGTGAGTCCAAA[A/C]CTGGGTAAAATACTG	55159
rs752978998	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658398	AATAAGCTCACTACT[C/T]AGCTTTCCATAGCTT	55159
rs753087972	snp	A/G	0.000181188	0.00951636	synonymous-codon	RFWD3	GRCh38.p7	16:74644370	CACCTACCTTTTCAT[A/G]CGCTCCTGTTCACTA	55159
rs753106420	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74627776	CTGTGAAAGGCAAAC[G/T]ATGAACACCCACAAC	55159
rs753139338	snp	C/T	4.97529e-05	0.00498738	intron-variant	RFWD3	GRCh38.p7	16:74632480	TTCCATGCTACTCAA[C/T]ACCAAAGAGCCCAGT	55159
rs753155721	snp	A/G	6.58903e-05	0.00573941	missense	RFWD3	GRCh38.p7	16:74644372	CCTACCTTTTCATGC[A/G]CTCCTGTTCACTAGT	55159
rs753277175	in-del	-/TCTCTCTCTA/TCTCTCTT			intron-variant	RFWD3	GRCh38.p7	16:74631470	GAGTGAGACTCTCTC[-/TCTCTCTCTA/TCTCTCTT]TCTCTCTCAAAAATA	55159
rs753361381	snp	C/G	1.64928e-05	0.00287161	missense	RFWD3	GRCh38.p7	16:74644649	CCCAGCATTGGTCCA[C/G]TGTTCCAGACATATT	55159
rs753376265	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634708	TAAATTCTTTAAAAA[C/T]ACGTCAAATCCTAGA	55159
rs753388835	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644898	TCATTCTTTCTAGAA[C/T]GCAATGTCACAAAAT	55159
rs753405875	snp	C/T			synonymous-codon	RFWD3	GRCh38.p7	16:74661102	GGTCATTGAATGCAA[C/T]GAAGATGCTGGGATG	55159
rs753446117	snp	A/G	1.6996e-05	0.00291508	intron-variant	RFWD3	GRCh38.p7	16:74632677	TAACACCAAAGCCTG[A/G]AAAAGGCAAAATAGT	55159
rs753447458	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74633166	CCTGTAATCCCAGCT[A/C]TTCAGGAGGCTGAGG	55159
rs753505232	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660178	GTGCTAACTCCTCTA[C/T]TCTATAGTTATGAGA	55159
rs753579357	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74629933	CCATCCTCAGAACTT[C/G]GGCTCACTTTATAAA	55159
rs753673810	snp	A/C	1.65655e-05	0.00287793	missense	RFWD3	GRCh38.p7	16:74628664	AGGGAGACCAGTGGG[A/C]ATCTGAAAGGAAAGT	55159
rs753675969	snp	C/T	1.84181e-05	0.00303458	intron-variant	RFWD3	GRCh38.p7	16:74637853	TAGAAAGGACAAACG[C/T]ACCTGAACACGCCTT	55159
rs753687194	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74641509	ATATTATCAAGAAAT[A/T]GAAATGAAAAAAACT	55159
rs753708335	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623696	AGGCTTTAAACCCAA[C/G]AAATGGATAATGTAG	55159
rs753796653	snp	A/G	1.76117e-05	0.00296741	intron-variant	RFWD3	GRCh38.p7	16:74630758	AGCTGCTACCACCAG[A/G]AAAAGAGTGAGTGGC	55159
rs753806134	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	RFWD3	GRCh38.p7	16:74644556	CTGGGGACATTTTCG[C/T]ACTTGTCCTTTAAGC	55159
rs753806479	snp	C/T	1.64732e-05	0.0028699	missense	RFWD3	GRCh38.p7	16:74661184	ATGTTCTCCACAGTG[C/T]CTTCTCCCAAGACCT	55159
rs753896173	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661105	CATTGAATGCAACGA[A/G]GATGCTGGGATGGTG	55159
rs753986351	snp	C/G	1.73721e-05	0.00294716	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74661450	TGCTTCATGAGCCAT[C/G]ACTAGAGAAACAGTA	55159
rs754024501	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647448	ACGCACCACCATATC[C/T]GGCTAATTTTTGTAT	55159
rs754052432	snp	G/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623012	TTGTAAATTCTCTTA[G/T]GTCTTTTCTCCTGAT	55159
rs754057698	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74659260	ACTGAGGACTTGCAA[C/G]AGGCCTCCTGACAGT	55159
rs754138211	snp	C/T	6.59348e-05	0.00574135	missense	RFWD3	GRCh38.p7	16:74623977	GTTAAGGTAGCCAAG[C/T]AGCTGTTACGGTTCA	55159
rs754184350	snp	A/G	4.96167e-05	0.00498055	synonymous-codon	RFWD3	GRCh38.p7	16:74652098	CCTGCTCACCTGAAA[A/G]TAAGCATCCAATGGT	55159
rs754238912	in-del	-/AA	1.79005e-05	0.00299164	intron-variant	RFWD3	GRCh38.p7	16:74630749	CAAGAGAAAGCTGCT[-/AA]ACCACCAGGAAAAGA	55159
rs754248066	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627825	CAGGACAGGGCTAGA[A/G]TTTATAGCCACTCTC	55159
rs754277636	in-del	-/AGATAGATAGA			intron-variant	RFWD3	GRCh38.p7	16:74666212	GATAGATAGATAGAT[-/AGATAGATAGA]TTGATTAGATACATA	55159
rs754278440	snp	G/T	1.64817e-05	0.00287064	synonymous-codon	RFWD3	GRCh38.p7	16:74626511	GTCATCCAGTCGGTA[G/T]GACATTTCCATCAGC	55159
rs754307516	snp	C/G	1.77805e-05	0.0029816	intron-variant	RFWD3	GRCh38.p7	16:74660892	GTTTCATAATTTCTA[C/G]TACAGCAATGATCAC	55159
rs754326769	in-del	-/AA	1.64849e-05	0.00287092	frameshift-variant	RFWD3	GRCh38.p7	16:74636353	CTCTTTACCTGGAAG[-/AA]AAGAGGCCTGAGGAG	55159
rs754402130	snp	A/G	1.85393e-05	0.00304455	synonymous-codon	RFWD3	GRCh38.p7	16:74637948	CGGCCTGTTTCCTTA[A/G]CATCTGTTCCTTCAG	55159
rs754422070	in-del	-/AGA			intron-variant	RFWD3	GRCh38.p7	16:74666216	GATAGATAGATAGAT[-/AGA]TAGATTGATTAGATA	55159
rs754427373	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74642811	TTATTTTCAAAAAGG[A/C]TCAAAGCAATATGGC	55159
rs754446035	snp	A/G	1.69887e-05	0.00291446	intron-variant	RFWD3	GRCh38.p7	16:74632679	ACACCAAAGCCTGAA[A/G]AAGGCAAAATAGTAT	55159
rs754446371	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74649743	TTGCAATCAGAATCC[-/A]AAAAAAAGTCTCCAT	55159
rs754469109	snp	A/G	3.2956e-05	0.00405918	synonymous-codon	RFWD3	GRCh38.p7	16:74632600	AAACGCCAGTCCACG[A/G]ATCTGTTTGCCATGC	55159
rs754481494	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74632005	TTTCAAAGAAACAGG[A/C]AACATACAGTTTTGT	55159
rs754532759	in-del	-/ACC	0.000329419	0.0128297	intron-variant	RFWD3	GRCh38.p7	16:74644352	GCCAGGCATACTCTT[-/ACC]ACCACCTACCTTTTC	55159
rs754556807	snp	C/T	1.65051e-05	0.00287267	synonymous-codon	RFWD3	GRCh38.p7	16:74626523	GTAGGACATTTCCAT[C/T]AGCACACTTCGTATG	55159
rs754620664	in-del	-/TGTCTTTATAG	1.74152e-05	0.00295082	intron-variant	RFWD3	GRCh38.p7	16:74652154	CAACGGAATTATAGT[-/TGTCTTTATAG]ACAATGAACTATCAT	55159
rs754620852	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668505	GTTTTCATCTACATA[G/T]GTTCCTAAGTATGTT	55159
rs754709507	snp	A/G	1.74136e-05	0.00295067	intron-variant	RFWD3	GRCh38.p7	16:74630765	ACCACCAGGAAAAGA[A/G]TGAGTGGCTCCCTAC	55159
rs754717577	snp	A/T	1.64732e-05	0.0028699	synonymous-codon	RFWD3	GRCh38.p7	16:74626442	CAATAGTTTGCAAGT[A/T]GGTCCTCCAAAAAAT	55159
rs754721218	in-del	-/CA			intron-variant	RFWD3	GRCh38.p7	16:74644240	ACTGCCAATGATCCC[-/CA]GAGATCCCAAGTCAC	55159
rs754755994	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648709	CACGGGAGGCAGAGG[C/T]TATTGTGGTGAGCTG	55159
rs754795685	snp	C/T	1.81089e-05	0.00300901	synonymous-codon	RFWD3	GRCh38.p7	16:74637856	AAAGGACAAACGTAC[C/T]TGAACACGCCTTTGA	55159
rs754851405	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623071	AGCTTTGACCTATCA[C/T]TCATCTTTTCCTGGC	55159
rs754873841	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74647650	AAGCTAGAGCGCAGT[A/G]ACGCTATTTGGGCTC	55159
rs754899066	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657908	ATTTAATCAAATACA[C/T]ACTAGAGTTAGGGTG	55159
rs754964715	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645362	CTCATGGATATATAG[C/T]CATGCATTGCTTGAC	55159
rs755008299	snp	A/C	1.64732e-05	0.0028699	missense	RFWD3	GRCh38.p7	16:74661192	CACAGTGTCTTCTCC[A/C]AAGACCTCCACTTCT	55159
rs755010961	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623836	CCAATGTTCTAGACT[A/G]CAGACAATAAACAGG	55159
rs755058477	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645403	CATTCTGAGAAATGC[A/G]TCTTTAGGCGATTTC	55159
rs755090342	snp	C/T	1.65345e-05	0.00287524	missense	RFWD3	GRCh38.p7	16:74661320	CCCCCTGGCTGCTGA[C/T]CACATCAGCAGGAAC	55159
rs755134235	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74629861	CTCCCTTTTTGATAA[C/G]TTTATACCTACAGGG	55159
rs755146376	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74643448	AATGAAGTTTCATTA[A/C]GTAAATCTTGGTACA	55159
rs755153249	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634839	AGGGGGGCGCAGGTA[C/T]AGGCTTTAAATCAAC	55159
rs755161198	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74656496	ATTCTTTTTTTTTCT[A/T]TTTGGAGACAGGGTC	55159
rs755204824	in-del	-/AAAT			intron-variant	RFWD3	GRCh38.p7	16:74649086	CTAGTCTCTAAAAAT[-/AAAT]AAATAAATAAATAAA	55159
rs755233927	snp	A/G	1.6476e-05	0.00287014	missense	RFWD3	GRCh38.p7	16:74649184	ACTTCTTGCTCTGCT[A/G]AGACACCTGCTAGTT	55159
rs755293919	snp	C/G	3.72578e-05	0.00431596	missense	RFWD3	GRCh38.p7	16:74637949	GGCCTGTTTCCTTAG[C/G]ATCTGTTCCTTCAGT	55159
rs755312430	snp	C/T	3.31203e-05	0.00406928	missense	RFWD3	GRCh38.p7	16:74652105	ACCTGAAAGTAAGCA[C/T]CCAATGGTGCTCTCA	55159
rs755356392	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74661529	AGAATCATATTTAAT[C/G]TTTCTGATTTTATGT	55159
rs755362516	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74659920	ATCGGCATGGTTGCG[-/T]TATGCCTGTAGTCCC	55159
rs755368575	snp	A/T	1.77773e-05	0.00298133	intron-variant	RFWD3	GRCh38.p7	16:74660893	TTTCATAATTTCTAG[A/T]ACAGCAATGATCACA	55159
rs755477729	snp	A/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662373	ATGGGGGTTCAACTA[A/C]TAGTTATTAAGCACC	55159
rs755532391	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74635590	ACACGTTAAGAAAAA[A/C]AGAACAGAACACATT	55159
rs755545140	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74651517	CCAGTTAGTGGGGAG[A/G]CTGAGGTGGGAGGAT	55159
rs755556482	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74633107	CACAGTGAAACCCTG[A/T]CTCTACTAAAACACA	55159
rs755561731	snp	G/T	2.98147e-05	0.00386089	intron-variant	RFWD3	GRCh38.p7	16:74638006	ACAAGTGGGGATTAG[G/T]AAGGCTACAGAAGAC	55159
rs755594453	snp	A/T	1.64735e-05	0.00286993	missense, intron-variant	RFWD3	GRCh38.p7	16:74630868	TTGGCCAGTCCAGCA[A/T]AGATGTAGTTAGCCT	55159
rs755600679	snp	C/G	1.64727e-05	0.00286986	synonymous-codon	RFWD3	GRCh38.p7	16:74644418	GGTTCGGGCATAAAG[C/G]ACGACAATGTCACTG	55159
rs755647088	snp	A/G	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74644549	TCCTTACCTGGGGAC[A/G]TTTTCGTACTTGTCC	55159
rs755700844	snp	A/C/T	0.000115306	0.00759216	missense	RFWD3	GRCh38.p7	16:74661092	TGATGAAGTTGGTCA[A/C/T]TGAATGCAACGAAGA	55159
rs755735708	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648770	ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAGA	55159
rs755752682	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74632107	AAAACAGAGCTAAGG[A/T]CGGCTGGGCGCAGTG	55159
rs755753338	snp	G/T	5.53879e-05	0.00526221	intron-variant	RFWD3	GRCh38.p7	16:74661480	ATTTGTAAAAAGTAT[G/T]AATAAAATAGATAAA	55159
rs755848003	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	RFWD3	GRCh38.p7	16:74632582	GCCTCTGAGGTAACT[A/G]CTAAACGCCAGTCCA	55159
rs755874703	snp	A/G	1.65018e-05	0.00287239	missense	RFWD3	GRCh38.p7	16:74628479	TCACAAGACAGTGCC[A/G]GGAGCTGTTCTCTGT	55159
rs755880978	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74638828	CATGTTCTGAGAAAC[A/G]TGTTGTTAGGTGATT	55159
rs755894602	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74640267	TCTTCTGACTCAGCA[A/T]CCTGAGTAGCTGGGA	55159
rs755931358	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74651826	TAGGGGAGAAAAGGG[-/A]AAGTGTCAAAGCACA	55159
rs755970373	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629150	TTCCTTCTGCAAGCA[C/T]ATGACCAGGACTATG	55159
rs755975641	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622282	AGGAGTATCTCCTCT[A/G]AGAAAAGAGCTTTTC	55159
rs755986458	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665646	CACCTGTGGTCCCAG[C/G]TATTGCGGGAAGCCG	55159
rs756037906	in-del	-/T	3.53485e-05	0.00420393	intron-variant	RFWD3	GRCh38.p7	16:74644786	AATGTAAAATCAATC[-/T]TGAAGAAGATGTGCA	55159
rs756054495	in-del	-/TGT	1.64731e-05	0.00286989	cds-indel	RFWD3	GRCh38.p7	16:74661145	TCAGATCCCTGCCTA[-/TGT]TGTTCTGAAGTTCTT	55159
rs756056745	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659579	CAGCCTGAGTGACAG[A/G]GCAAGACTCTTGTCT	55159
rs756065089	snp	A/C	1.65367e-05	0.00287543	missense	RFWD3	GRCh38.p7	16:74628639	TGAGGCAGCTCTGGG[A/C]ATGTATGACAGGGAG	55159
rs756076219	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74665201	CCTGTGATCCCTGGA[C/T]ACTGAAATGCCCAGG	55159
rs756084322	snp	C/T	3.29478e-05	0.00405867	missense, intron-variant	RFWD3	GRCh38.p7	16:74630853	ACCAGAATTGAACCA[C/T]TGGCCAGTCCAGCAT	55159
rs756091925	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74635791	AACATCTGCAAGATT[C/T]AGAAATGATTTAATT	55159
rs756115980	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74639472	CACGTGACTGTAAAG[-/T]TAAAAGGCTAGGCAG	55159
rs756119781	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650195	TGTTAAATTTCCATA[C/T]ATATTTAGGTCTAGA	55159
rs756160301	snp	C/T	8.23649e-05	0.00641683	missense	RFWD3	GRCh38.p7	16:74660999	ATACCCTCCTTCTTG[C/T]TCTCATTGGCCCTAC	55159
rs756167114	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74647412	CCTGCCTCAGCTTCC[C/G]GAGTAGCTGGGACTA	55159
rs756255228	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636855	AGCTGGGATTACATG[C/T]ACCCACTACCATGCC	55159
rs756287086	snp	C/T	7.09786e-05	0.00595687	missense	RFWD3	GRCh38.p7	16:74637936	CTGATTCTAACTCGG[C/T]CTGTTTCCTTAGCAT	55159
rs756288230	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646355	CACTCCAGCATGAGG[A/G]ACAGAATGAGACCCT	55159
rs756329608	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658408	CTACTTAGCTTTCCA[C/T]AGCTTTGGCTTCTTG	55159
rs756332506	snp	G/T	3.29658e-05	0.00405978	synonymous-codon	RFWD3	GRCh38.p7	16:74623967	CATCTTCTCTGTTAA[G/T]GTAGCCAAGTAGCTG	55159
rs756365758	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627790	CTATGAACACCCACA[A/G]CGAACTCCCTAGTGT	55159
rs756366559	snp	C/G	3.30284e-05	0.00406363	missense	RFWD3	GRCh38.p7	16:74661308	GGATGGATGGTACCC[C/G]CTGGCTGCTGACCAC	55159
rs756415611	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	RFWD3	GRCh38.p7	16:74626430	GGCATTTTTGGTCAA[C/T]AGTTTGCAAGTAGGT	55159
rs756427264	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663580	GAAGTACATATATGT[A/G]TCTTTCTCTCTCCAC	55159
rs756465058	snp	C/G	1.65132e-05	0.00287339	missense, intron-variant	RFWD3	GRCh38.p7	16:74630931	CGTCCAGCATTATAA[C/G]TCTGGACCACGGTAT	55159
rs756470042	snp	A/T	1.66007e-05	0.00288098	missense	RFWD3	GRCh38.p7	16:74632658	TTGGCAGTACTCAAC[A/T]TCTTAACACCAAAGC	55159
rs756483811	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74643852	GCTAATTTTTTTGTA[-/T]TTTTTTAGTAGAGAC	55159
rs756505489	snp	C/T	1.65217e-05	0.00287412	intron-variant	RFWD3	GRCh38.p7	16:74626317	AAACTACTTTTTATA[C/T]GAAAGTAAAAAAGTA	55159
rs756542649	snp	C/G	6.59065e-05	0.00574012	missense	RFWD3	GRCh38.p7	16:74652014	AGAACTACTAGACAC[C/G]TGCAACTCTTCAGAT	55159
rs756652158	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653141	CCTAGGAGTTCGAGA[C/T]CAGCCTGATTAACAT	55159
rs756675450	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74626610	ACACAAAAAATTAAC[C/G]AAGTACCCAAACCTC	55159
rs756678157	snp	A/C			missense	RFWD3	GRCh38.p7	16:74661127	GGGATGGTGTGATTA[A/C]CATCAGATCCCTGCC	55159
rs756685003	snp	C/G	1.65266e-05	0.00287455	missense	RFWD3	GRCh38.p7	16:74652092	CTGGGTCCTGCTCAC[C/G]TGAAAGTAAGCATCC	55159
rs756687213	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74624625	TGGTCTAGAACTCCT[C/G]ACCTCAGGTGATCCA	55159
rs756729143	snp	C/T	6.94613e-05	0.00589286	intron-variant	RFWD3	GRCh38.p7	16:74660919	TCACAGACTTATCCA[C/T]ATATTTATTTACCTG	55159
rs756732813	snp	G/T	1.72639e-05	0.00293796	missense	RFWD3	GRCh38.p7	16:74637868	TACCTGAACACGCCT[G/T]TGAAGCCTAGTGCAC	55159
rs756744796	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74650460	ATTAGAGGCACATAT[A/G]GTCTTGCTGTCCTAT	55159
rs756752055	snp	A/G	1.64738e-05	0.00286995	intron-variant	RFWD3	GRCh38.p7	16:74644327	ACAATGAACCAAAAG[A/G]GAACATTCCAGCCAG	55159
rs756785516	snp	C/T	6.59174e-05	0.00574059	missense	RFWD3	GRCh38.p7	16:74660981	TTGCCCTCCGTGAAG[C/T]AGATACCCTCCTTCT	55159
rs756869700	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74638949	ACAAACTTGTATAGT[A/C]TGTTACCATAATGAA	55159
rs756889031	snp	C/G	1.73667e-05	0.0029467	missense	RFWD3	GRCh38.p7	16:74624061	AACGAGCCACTGGCA[C/G]CATCCCACAGCTAAA	55159
rs756933752	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	RFWD3	GRCh38.p7	16:74649168	TCCATCGATACATGT[A/G]ACTTCTTGCTCTGCT	55159
rs756942881	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74660266	CAGAGTGAGACTCCA[A/T]CTCAAAACAAAACAA	55159
rs756952497	snp	C/G	1.64727e-05	0.00286986	missense	RFWD3	GRCh38.p7	16:74644398	CTAGTGTCCAAAGCT[C/G]TCAGGGTTCGGGCAT	55159
rs757029951	in-del	-/GGA	0.000198791	0.00996774	cds-indel	RFWD3	GRCh38.p7	16:74661341	CAGCAGGAACAGGCT[-/GGA]GGAGGGCTGGTCCCC	55159
rs757030286	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74665959	TGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTACA	55159
rs757061135	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629961	AAACTTCTCAATCTC[A/G]TAACTGGATTAAATG	55159
rs757103371	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623722	TGTAGATAAAGTACC[C/T]ATCAATTACTCTTTT	55159
rs757108659	snp	C/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74620902	GGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG	55159
rs757213550	snp	C/T	1.75176e-05	0.00295947	missense	RFWD3	GRCh38.p7	16:74637863	AAACGTACCTGAACA[C/T]GCCTTTGAAGCCTAG	55159
rs757226708	snp	A/T	1.65274e-05	0.00287462	missense	RFWD3	GRCh38.p7	16:74628464	TACCAGGCCTGTAGG[A/T]CACAAGACAGTGCCG	55159
rs757318624	snp	C/T	3.37769e-05	0.00410942	missense	RFWD3	GRCh38.p7	16:74626552	TGGTGGTGTGATTTT[C/T]ATCTATGGGACAGAG	55159
rs757378855	snp	A/C	1.85129e-05	0.00304238	missense	RFWD3	GRCh38.p7	16:74636577	TAAGTTTTTGCAAGT[A/C]CTAAAATGAAAAAGA	55159
rs757432710	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	RFWD3	GRCh38.p7	16:74652011	ATCAGAACTACTAGA[C/T]ACCTGCAACTCTTCA	55159
rs757462514	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629827	GATACTTCAGATTTT[A/G]GCCAGGTCACAGACC	55159
rs757465140	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74648642	CTGGGCGGGGTGGCG[G/T]GTGCCTGTAGTCCCA	55159
rs757466462	snp	C/G	3.29685e-05	0.00405995	missense, intron-variant	RFWD3	GRCh38.p7	16:74630839	TTCGCACGTCATATA[C/G]CAGAATTGAACCATT	55159
rs757478195	snp	C/T	3.40698e-05	0.0041272	intron-variant	RFWD3	GRCh38.p7	16:74630778	GAGTGAGTGGCTCCC[C/T]ACCTGGCTTTCTGAG	55159
rs757500103	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664877	AACACTTTTCTCGTC[A/G]CACAAAGTTCTATGG	55159
rs757511140	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644116	AAGCAAAAATGGCAA[C/T]AGAAGTAATGTGCCA	55159
rs757554497	in-del	-/GAGT	3.49724e-05	0.0041815	intron-variant	RFWD3	GRCh38.p7	16:74630763	CTACCACCAGGAAAA[-/GAGT]GAGTGGCTCCCTACC	55159
rs757557494	snp	C/G	1.64781e-05	0.00287033	missense	RFWD3	GRCh38.p7	16:74632548	TAATAGTGTTGTCTA[C/G]GGAAGCAGAGAGTAG	55159
rs757588743	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663669	AAAGGATAAATTAAC[C/T]AGGACGACACAAATG	55159
rs757647684	snp	A/G	4.94222e-05	0.00497078	intron-variant	RFWD3	GRCh38.p7	16:74644502	TCTAGGAATCTGCCT[A/G]ACTTAACATGTTAAT	55159
rs757734124	snp	A/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668712	ACCCAACTGAATGGT[A/T]TCTCTTTGGCACATT	55159
rs757780989	in-del	-/TAGATAG			intron-variant	RFWD3	GRCh38.p7	16:74666215	AGATAGATAGATAGA[-/TAGATAG]ATTGATTAGATACAT	55159
rs757784111	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643055	TTATTTAAAAACGCT[A/G]CAAGTGAGCATTGGT	55159
rs757795659	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74652813	CTCCAGTTTGAGCTG[A/C]GGAGTTTGAGGCCAC	55159
rs757838675	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630703	CTAACTGTGGAACAC[C/T]CACTGAAGAGACGAT	55159
rs757845409	snp	A/C	1.65455e-05	0.00287619	intron-variant	RFWD3	GRCh38.p7	16:74626302	CCAATATTTTAAGCA[A/C]AACTACTTTTTATAT	55159
rs757871918	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640606	TCTGATGGCGCCACT[A/G]CACTCTGGCCTTTGT	55159
rs757885568	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74641645	ATAAAAACTTTCTGG[C/T]CGGGTGCAGTGCCTC	55159
rs757894888	snp	C/G	1.66363e-05	0.00288407	missense	RFWD3	GRCh38.p7	16:74652117	GCATCCAATGGTGCT[C/G]TCAACCTATGTACAC	55159
rs758006482	in-del	-/TT	1.69097e-05	0.00290768	intron-variant	RFWD3	GRCh38.p7	16:74630977	GGAGTTACAAAAGAC[-/TT]TTACAACTGCATTAA	55159
rs758012188	in-del	-/A	1.72068e-05	0.00293311	frameshift-variant	RFWD3	GRCh38.p7	16:74637923	GTCGGCACTGTGCTG[-/A]ATTCTAACTCGGCCT	55159
rs758019843	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74630179	CGGCTCACCGCAACC[G/T]CCGCCTCCGAGGCTC	55159
rs758049842	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74625299	GCTGAGGTGAGAAGA[C/G]TGCTTGAGCCCAGGA	55159
rs758102530	in-del	-/T			frameshift-variant	RFWD3	GRCh38.p7	16:74632603	GCCAGTCCACGGATC[-/T]TGTTTGCCATGCATC	55159
rs758120765	snp	A/G/T	6.6055e-05	0.00574663	missense	RFWD3	GRCh38.p7	16:74661301	GGCTGGAGGATGGAT[A/G/T]GTACCCCCTGGCTGC	55159
rs758121403	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74637057	CAAGCAAGTGAAATA[A/T]GGAGAGCACAGAATC	55159
rs758124847	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635047	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAT	55159
rs758187731	snp	A/G	1.65888e-05	0.00287996	intron-variant	RFWD3	GRCh38.p7	16:74628443	ATGGGAGACCCCAGC[A/G]CTACTTACCAGGCCT	55159
rs758235914	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74647576	TACAGGTGTGAGCCA[A/C]TGCGCCCGGCCAACA	55159
rs758278041	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74657933	AGGGTGTTGACACGT[A/G]TATCAATAGAATTCT	55159
rs758285366	in-del	-/TGTC			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623387	AAGTTACTAAAAGAT[-/TGTC]AGCCTTCAAGGTCAG	55159
rs758295708	snp	A/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623014	GTAAATTCTCTTATG[A/T]CTTTTCTCCTGATCT	55159
rs758358176	snp	G/T			missense	RFWD3	GRCh38.p7	16:74628517	TCTATGCAGCCCCCT[G/T]GCTCCAAGGGCAGCA	55159
rs758391825	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74625035	GAAAAATATTTTGAA[-/G]TATTAAAAAGTAGAG	55159
rs758425563	snp	C/T	3.60451e-05	0.00424515	intron-variant	RFWD3	GRCh38.p7	16:74661467	CTAGAGAAACAGTAT[C/T]TGTAAAAAGTATTAA	55159
rs758457947	snp	A/G	3.46075e-05	0.00415963	intron-variant	RFWD3	GRCh38.p7	16:74632688	CCTGAAAAAGGCAAA[A/G]TAGTATGAAATAGAT	55159
rs758500052	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74641164	AAACACAAACAGATA[A/T]TTTTTTTTTTTTTTG	55159
rs758599981	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74656420	TCTTAAGATGATAGC[G/T]GCCAGTGATTCCTCT	55159
rs758609766	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627922	CCAGGAATTTAGATT[C/T]ATGCCGCTTAGCCTA	55159
rs758642267	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74658738	ACATTTAAATTCTGT[A/G]TAACTCATTCCCTGA	55159
rs758670822	snp	C/T	1.64991e-05	0.00287215	missense	RFWD3	GRCh38.p7	16:74636555	AAATTCTGACTTTGA[C/T]GTGACGTAAGTTTTT	55159
rs758691698	snp	C/G	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644383	ATGCGCTCCTGTTCA[C/G]TAGTGTCCAAAGCTC	55159
rs758728283	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660431	GGAATCCAGCCTGGA[C/T]GACAGAGTGAGACGC	55159
rs758787506	snp	A/G	6.32391e-05	0.00562277	intron-variant	RFWD3	GRCh38.p7	16:74638017	TTAGGAAGGCTACAG[A/G]AGACTTCCCATCCAG	55159
rs758818276	snp	C/T	0.000181239	0.00951769	synonymous-codon	RFWD3	GRCh38.p7	16:74661252	CTGGAGCAGGGGTGG[C/T]GTCGCTTGGCTGCTG	55159
rs758901430	snp	A/T	1.66983e-05	0.00288944	missense	RFWD3	GRCh38.p7	16:74661396	AGGAGCTGGCTGTTG[A/T]TCGGCATGATTTAAC	55159
rs758907378	snp	A/C	1.73691e-05	0.00294691	missense	RFWD3	GRCh38.p7	16:74624062	ACGAGCCACTGGCAG[A/C]ATCCCACAGCTAAAG	55159
rs758926227	in-del	-/AAC			intron-variant	RFWD3	GRCh38.p7	16:74632414	AAAACAAAACAAAAC[-/AAC]AACAACAACAACAAA	55159
rs758991929	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74654880	AATCCCTAATCCAGA[C/G]GAAGGCCCCAACTCT	55159
rs759000533	snp	A/G	1.65703e-05	0.00287834	intron-variant	RFWD3	GRCh38.p7	16:74632481	TCCATGCTACTCAAC[A/G]CCAAAGAGCCCAGTC	55159
rs759032154	snp	A/G	1.65105e-05	0.00287315	missense	RFWD3	GRCh38.p7	16:74624005	TCACCTCAAATGGGC[A/G]GATGTCCAACACAGG	55159
rs759052833	snp	A/G	0.000152293	0.00872487	intron-variant	RFWD3	GRCh38.p7	16:74644750	GCTAGATGGAAAGCA[A/G]AATATATTCAAATTA	55159
rs759098882	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623341	AAAGCACACCCAGGT[A/G]TGCTATCACACACTT	55159
rs759144486	snp	A/C	1.64893e-05	0.0028713	synonymous-codon	RFWD3	GRCh38.p7	16:74661282	GATCACCTCAGCAGG[A/C]GCTGGCTGGAGGATG	55159
rs759170848	snp	A/G	1.66222e-05	0.00288285	intron-variant	RFWD3	GRCh38.p7	16:74636315	TGGAGTCTAATAAAG[A/G]ACATGAAAGCTGAGG	55159
rs759194011	snp	C/T	4.94181e-05	0.00497057	missense	RFWD3	GRCh38.p7	16:74636420	CAGTATGCCATGATC[C/T]GGCAGTTTCCTGCCT	55159
rs759277374	snp	C/T	1.65007e-05	0.00287229	synonymous-codon	RFWD3	GRCh38.p7	16:74652065	ATCATAAGTGGTAGC[C/T]GGCAAGTCAGGCTGG	55159
rs759291910	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74649938	ATATAATAAATTGAG[C/T]ATTGTGCAACCACCA	55159
rs759304953	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74660618	GGAATGCCAGTGAAT[-/A]ATGAATTTGGGTGAG	55159
rs759317365	snp	A/G	1.64811e-05	0.00287059	synonymous-codon	RFWD3	GRCh38.p7	16:74649144	TACCTGTTTGGGGAG[A/G]GTCTTGCCTCCATCG	55159
rs759327850	snp	A/G	1.6591e-05	0.00288015	intron-variant	RFWD3	GRCh38.p7	16:74628674	GTGGGCATCTGAAAG[A/G]AAAGTAAGGAAACTG	55159
rs759445891	snp	A/C/G	3.29485e-05	0.00405874	missense, intron-variant	RFWD3	GRCh38.p7	16:74630911	AGCAACAGCTCCAGA[A/C/G]AGGACGTCCAGCATT	55159
rs759451651	snp	A/G	4.9423e-05	0.00497082	missense	RFWD3	GRCh38.p7	16:74644591	TGGAAATGCACCTAT[A/G]CCCAAAGAGATGCCC	55159
rs759459724	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74634065	AAAAGTCATCAAATT[A/G]TATACTTTAAATATG	55159
rs759495974	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632901	ACAACTTCTGCCTCC[C/T]GGTGATCTGCTCGCC	55159
rs759537437	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630831	GCTCGTGTTTCGCAC[A/G]TCATATACCAGAATT	55159
rs759555438	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631603	AGTACTCACAGAGCA[C/T]GTGACAGATAAAACG	55159
rs759556308	in-del	-/AA/AAA			intron-variant	RFWD3	GRCh38.p7	16:74637122	CGTTTAAAGTCCTTT[-/AA/AAA]AAAAAAAAAAAAAAA	55159
rs759578083	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658262	AGGGCAAAGTTTAGT[C/T]TCTCACACAGAGGAG	55159
rs759592059	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74630643	ATGTTATTGATTCTG[A/C]AGTGAGATCAAGTGG	55159
rs759606092	snp	A/G	1.64735e-05	0.00286993	intron-variant	RFWD3	GRCh38.p7	16:74644473	AGAACCCAATAGGAC[A/G]TAATTAGAGTGGTTC	55159
rs759607030	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74666705	GGTGTCTCCTGAATC[C/G]CAATCCAGGAATCAG	55159
rs759634055	snp	C/T	0.000199058	0.00997443	intron-variant	RFWD3	GRCh38.p7	16:74632475	ACGAATTCCATGCTA[C/T]TCAACACCAAAGAGC	55159
rs759635591	snp	A/C			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621661	ATGTGATGTCCTACA[A/C]CGGGGACTGGGAATG	55159
rs759696171	snp	C/G	1.64732e-05	0.0028699	synonymous-codon	RFWD3	GRCh38.p7	16:74661009	TCTTGTTCTCATTGG[C/G]CCTACACTGTGGTTT	55159
rs759707009	in-del	-/CACG	1.64787e-05	0.00287038	frameshift-variant	RFWD3	GRCh38.p7	16:74632595	TGCTAAACGCCAGTC[-/CACG]CACGGATCTGTTTGC	55159
rs759746609	in-del	-/T	3.29663e-05	0.00405981	frameshift-variant	RFWD3	GRCh38.p7	16:74628516	GTCTATGCAGCCCCC[-/T]GGCTCCAAGGGCAGC	55159
rs759799483	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667498	CAGTCTCAAATCACT[G/T]GTTAGGGCCGCCGCT	55159
rs759809190	snp	A/C	2.21648e-05	0.00332895	intron-variant	RFWD3	GRCh38.p7	16:74624115	AGGAGTCAGTCAGTA[A/C]ACGAAGGGACTTCCA	55159
rs759811432	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74643300	TTTTTTCTAGTTCAC[-/A]AAAATGCAATCATAC	55159
rs759844725	snp	C/G	3.50533e-05	0.00418634	intron-variant, splice-acceptor-variant	RFWD3	GRCh38.p7	16:74661455	CATGAGCCATCACTA[C/G]AGAAACAGTATTTGT	55159
rs759895834	snp	C/T	1.66241e-05	0.00288302	intron-variant	RFWD3	GRCh38.p7	16:74628437	TAAGCTATGGGAGAC[C/T]CCAGCACTACTTACC	55159
rs759902600	snp	C/T	1.64969e-05	0.00287196	missense	RFWD3	GRCh38.p7	16:74632523	CCCCAAATCACTCAC[C/T]TGGTCAGTTTAATAG	55159
rs759914662	snp	A/G	4.94181e-05	0.00497057	missense	RFWD3	GRCh38.p7	16:74636421	AGTATGCCATGATCC[A/G]GCAGTTTCCTGCCTG	55159
rs759951933	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647245	TGGAAGAATTCACAG[C/T]AGATGTAAATTACTC	55159
rs759961288	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654983	GTTTAAGAAAAGATA[C/T]TGTCTCCATAAAGTG	55159
rs759964125	snp	A/G	1.64933e-05	0.00287165	missense	RFWD3	GRCh38.p7	16:74628577	TGTTCCCAGAATGAA[A/G]CATCCTCCAAGGTTC	55159
rs760002725	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74637581	GAGGTTGCAGTGAGC[C/G]GAGATCACATCACTG	55159
rs760003856	snp	A/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622653	AACAACTCTTCAATA[A/C]TCATTTGAGAAAATC	55159
rs760013649	snp	A/G	1.65644e-05	0.00287783	stop-gained	RFWD3	GRCh38.p7	16:74660951	CACTGTCTGTCCTCT[A/G]AGACCCTCCGGCTCT	55159
rs760038840	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663525	GGCCAGACTGGTGCA[A/G]GCTGAATAAATGGAA	55159
rs760056385	snp	A/G	1.65015e-05	0.00287237	stop-gained, intron-variant	RFWD3	GRCh38.p7	16:74630827	GACTGCTCGTGTTTC[A/G]CACGTCATATACCAG	55159
rs760077932	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659109	TGTTTGGCTCTCTAG[C/T]GGTTCTGTTTTTCTT	55159
rs760118115	snp	A/G	1.66427e-05	0.00288462	missense	RFWD3	GRCh38.p7	16:74644729	GCTCAGACTTCTGGG[A/G]AGATGGCTAGATGGA	55159
rs760258385	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661177	TGGATTGATGTTCTC[C/T]ACAGTGTCTTCTCCC	55159
rs760259781	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645827	GCAGAATCTCGGCTC[A/G]CTGCAAGTTCCGCCT	55159
rs760295484	in-del	-/TC			intron-variant	RFWD3	GRCh38.p7	16:74658261	TAGGGCAAAGTTTAG[-/TC]TCTCACACAGAGGAG	55159
rs760303768	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74644270	ACAGGTCAAGTAAAA[A/C]CTCACTACGAGTGAC	55159
rs760335502	in-del	-/AAA			intron-variant, cds-indel	RFWD3	GRCh38.p7	16:74662139	CCTAGTTTTTAAACT[-/AAA]AAAAAAAATTTTTTT	55159
rs760398245	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	RFWD3	GRCh38.p7	16:74651975	AACCCCTCCATACTC[C/T]GCAGAGCTGTCACTG	55159
rs760399666	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663094	TATTTTTAGTACAGC[C/T]GGGGTTTCACTGTGT	55159
rs760486131	snp	C/G	1.65908e-05	0.00288012	intron-variant	RFWD3	GRCh38.p7	16:74651898	TTAGCCTTGTGAGTC[C/G]AAACCTGGGTAAAAT	55159
rs760491130	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74651551	TTGAGCCCAAGAAGC[A/G]GAAGTTGCAGTAAGC	55159
rs760505640	snp	C/T	3.29457e-05	0.00405854	missense	RFWD3	GRCh38.p7	16:74626372	CTGCTTCATCCCCAG[C/T]ACACACCAGGATGTT	55159
rs760581202	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652600	CTCATTTTAGGATAG[C/T]ATTTTTCTTTTAAAA	55159
rs760629789	snp	C/T	1.68986e-05	0.00290672	intron-variant	RFWD3	GRCh38.p7	16:74628718	AAAACTCGGACGGCT[C/T]CAGACCCCACTACCA	55159
rs760667804	snp	C/G	2.05324e-05	0.00320403	intron-variant	RFWD3	GRCh38.p7	16:74637840	AAGTTCTTTGGATTA[C/G]AAAGGACAAACGTAC	55159
rs760667935	snp	C/T	1.64836e-05	0.0028708	missense	RFWD3	GRCh38.p7	16:74652040	CAGATACAGGATTCC[C/T]AGTCTCTGAATCATA	55159
rs760671888	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74625059	AGTAGAGCTAGCCGG[A/G]CATGGTGGCACACAC	55159
rs760679957	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623531	AGGATACTTAAGTGA[C/G]AGGACAACTCAGATG	55159
rs760693244	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74659201	TTGACCAAGAGGAAT[A/C]CACTCTGCGTCCCCC	55159
rs760711148	in-del	-/CTAG	1.65334e-05	0.00287514	intron-variant	RFWD3	GRCh38.p7	16:74636332	ATGAAAGCTGAGGTT[-/CTAG]CTAGACTCTTTACCT	55159
rs760743044	snp	C/G	1.66515e-05	0.00288539	missense	RFWD3	GRCh38.p7	16:74660944	TACCTGGCACTGTCT[C/G]TCCTCTGAGACCCTC	55159
rs760782276	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648248	CAGCAGTCACACAAA[C/T]AATGAGTAACTGGGA	55159
rs760808552	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668405	AAGCAACTACACCAA[C/T]AAGAATTAGTGCTAG	55159
rs760900416	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74646472	TGCCACCATACACCA[A/C]CCATGCTTTACATGA	55159
rs760941016	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74666593	CCAGATACGCGCGGG[C/G]GTTCGGGCTCCTTAG	55159
rs760951318	snp	A/G	1.76207e-05	0.00296817	intron-variant	RFWD3	GRCh38.p7	16:74631007	AAGAAAATCAAATAC[A/G]TGACAAAGATGTAAA	55159
rs760953231	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631699	TCTGTTACACAGAAT[C/T]ATCCAGGTAACAGAC	55159
rs761042662	snp	A/T	1.66515e-05	0.00288539	intron-variant	RFWD3	GRCh38.p7	16:74636310	ATATATGGAGTCTAA[A/T]AAAGAACATGAAAGC	55159
rs761073501	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637621	CTAGGTGACAGAGTG[A/G]GACTCTGCCTCAAAA	55159
rs761121983	in-del	-/TGTTTTTTTTTTT			intron-variant	RFWD3	GRCh38.p7	16:74643668	GGTGTTACTAGCAAC[-/TGTTTTTTTTTTT]TTTTTTTTTTTTTGA	55159
rs761136585	snp	A/G	1.6676e-05	0.00288751	missense	RFWD3	GRCh38.p7	16:74644734	GACTTCTGGGGAGAT[A/G]GCTAGATGGAAAGCA	55159
rs761144873	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74654940	GAAGCTGCAGGAAGT[A/T]GGAAGAAAGCAGAGG	55159
rs761148399	snp	A/T	1.67044e-05	0.00288997	intron-variant	RFWD3	GRCh38.p7	16:74628420	ACCACTGTGCTCCCA[A/T]ATAAGCTATGGGAGA	55159
rs761171705	snp	C/T	2.33141e-05	0.00341416	intron-variant	RFWD3	GRCh38.p7	16:74637805	ACTAACATTAGCTTC[C/T]TCTTCCATTCCTATT	55159
rs761191167	in-del	-/GCTGCT	1.80709e-05	0.00300585	intron-variant	RFWD3	GRCh38.p7	16:74630744	ATAAGCCAAGAGAAA[-/GCTGCT]ACCACCAGGAAAAGA	55159
rs761219849	in-del	-/AG			intron-variant	RFWD3	GRCh38.p7	16:74638038	TCCCATCCAGGTGGC[-/AG]AGTTAAGTTCATGCT	55159
rs761318670	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646719	TGAACTCAGGAGGTG[A/G]AAAGAAAAGAATTAA	55159
rs761329144	snp	A/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621308	AACAAACCCGAGAAA[A/T]CTACCAGGTTGGGAT	55159
rs761346553	snp	A/C	1.64743e-05	0.00287	stop-gained	RFWD3	GRCh38.p7	16:74651969	GTCAACAACCCCTCC[A/C]TACTCTGCAGAGCTG	55159
rs761352484	snp	A/G	1.65108e-05	0.00287317	missense	RFWD3	GRCh38.p7	16:74628613	AGCACCCCACCATAT[A/G]GAAATGCAGCTGAGG	55159
rs761406347	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636096	TATCAGTAACCTACA[C/T]TTCCAAGGACCTCAC	55159
rs761443691	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74626799	ATCTACAATAGCTTT[C/T]TGCTTAAGAGAAAAA	55159
rs761470028	snp	C/G	1.70507e-05	0.00291977	missense	RFWD3	GRCh38.p7	16:74624044	TCTGTAGGTCCTGGA[C/G]CAACGAGCCACTGGC	55159
rs761488176	in-del	-/TTAGG			intron-variant	RFWD3	GRCh38.p7	16:74629120	AGAAACAGGACTGTT[-/TTAGG]TTTTCTAAATTTCCT	55159
rs761507177	in-del	-/AATT			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662148	TAAACTAAAAAAAAA[-/AATT]TTTTTTTGTTATATA	55159
rs761591977	snp	C/T	1.69553e-05	0.00291159	missense	RFWD3	GRCh38.p7	16:74661434	GAACATCATATTCCA[C/T]TGCTTCATGAGCCAT	55159
rs761638582	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641525	GAAATGAAAAAAACT[A/G]GAGTCCCATGTATCA	55159
rs761652477	snp	C/G/T	3.30438e-05	0.0040646	intron-variant	RFWD3	GRCh38.p7	16:74632509	GTCTCCACCTACTTC[C/G/T]CCAAATCACTCACCT	55159
rs761677193	in-del	-/T	1.64735e-05	0.00286993	frameshift-variant	RFWD3	GRCh38.p7	16:74626458	GTCCTCCAAAAAATG[-/T]TATGTACAGGCTGGC	55159
rs761704287	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74626047	AAAAATCAGTCGGGC[A/T]TGGTGGTGGGGTGCC	55159
rs761710688	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640375	GGTCTCGAACTTCCG[A/G]CCTTGTGATCCGCCC	55159
rs761772447	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645143	TGCAAATTAAAGAGA[C/T]CATTTTTCATCTATC	55159
rs761790005	snp	A/G	1.66308e-05	0.00288359	intron-variant	RFWD3	GRCh38.p7	16:74651885	AGCTTCATGGATGTT[A/G]GCCTTGTGAGTCCAA	55159
rs761802969	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74652688	AATAACTTAGAATGA[G/T]GAGAAGACCTGGGGC	55159
rs761813439	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631851	GTCTCAAACCCCTGA[C/T]CTCAGCTGATTGCCT	55159
rs761907365	snp	C/T	4.94287e-05	0.00497111	missense	RFWD3	GRCh38.p7	16:74626491	GAGCAGATTGGATTT[C/T]CAGTGTCATCCAGTC	55159
rs761907882	snp	A/G	1.64781e-05	0.00287033	intron-variant	RFWD3	GRCh38.p7	16:74637983	GAACTAGAGGGGGAA[A/G]GCCAGCAACAAGTGG	55159
rs761910531	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638487	AAAGGACACATTCAC[C/T]AAGAATAACAAATAT	55159
rs762088780	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659969	TGAGGTAGGAAGATC[A/G]CCTAAGCCTGGGGAG	55159
rs762105678	snp	C/T	1.64765e-05	0.00287019	missense	RFWD3	GRCh38.p7	16:74644608	CCAAAGAGATGCCCA[C/T]AGCGTAATGCTGAGA	55159
rs762199789	snp	C/T	6.58892e-05	0.00573936	missense	RFWD3	GRCh38.p7	16:74626395	AGGATGTTGCCATCA[C/T]TCTCTGGGCTTTGGA	55159
rs762200019	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74628907	AGAAAAGGAAAAAAA[A/G]AACTAGGAAATTTAA	55159
rs762261419	in-del	-/T	7.68315e-05	0.00619757	intron-variant	RFWD3	GRCh38.p7	16:74649105	AAATAAATAAATAGA[-/T]TTTTTTTAAAATGAT	55159
rs762266092	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74665439	AAAAACTACCCGGGT[A/G]TGGTGGCGCATGCCT	55159
rs762268678	snp	A/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74661169	GAAGTTCTTGGATTG[A/T]TGTTCTCCACAGTGT	55159
rs762287541	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639458	AAGGTCATTATGCAG[C/T]ACGTGACTGTAAAGT	55159
rs762306758	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657310	GAGATTCGGCTGTTT[C/T]TCTTTAATAATCACT	55159
rs762367017	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74638190	ACTAGAAAATGGGGA[A/C]TAAAAATGCCACAGG	55159
rs762400176	snp	A/C	1.67618e-05	0.00289493	missense	RFWD3	GRCh38.p7	16:74661415	GCATGATTTAACTGC[A/C]CCTGAACATCATATT	55159
rs762446827	snp	C/G			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662237	CATGCATCAGGACAA[C/G]AGGACTGAGCCACTG	55159
rs762490667	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RFWD3	GRCh38.p7	16:74636425	TGCCATGATCCGGCA[A/G]TTTCCTGCCTGAGAT	55159
rs762540126	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74627591	CTGAACCTAACTTGT[A/T]TCCTAGTCAGGGCTC	55159
rs762552515	snp	A/C/G	0.000197709	0.00994081	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74649159	GGTCTTGCCTCCATC[A/C/G]ATACATGTAACTTCT	55159
rs762564615	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74653565	CGCCTATAATCCCAG[C/G]ACTCTGGAAAGCCAA	55159
rs762604190	snp	A/G	4.94564e-05	0.0049725	missense, intron-variant	RFWD3	GRCh38.p7	16:74630917	AGCTCCAGACAGGAC[A/G]TCCAGCATTATAAGT	55159
rs762704120	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659271	GCAAGAGGCCTCCTG[A/G]CAGTCAGCCAGCTCC	55159
rs762746123	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74629663	AAAACCACTACCACC[-/A]ACAAAAAAAAAAAAC	55159
rs762757836	snp	A/C	1.64757e-05	0.00287012	missense	RFWD3	GRCh38.p7	16:74636514	AGCAGCTCAGGACCC[A/C]TGCTTGGGAGCCCCT	55159
rs762766299	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631750	ACCAACCTGGTATGG[C/T]GACTCTGATGTCAGG	55159
rs762839868	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668448	AATCAAAGGAGCTGC[A/C]GGCCGGCCATTAGAA	55159
rs762877712	snp	C/G	3.29886e-05	0.00406118	missense	RFWD3	GRCh38.p7	16:74623943	TCACTCCCACTTATA[C/G]ATGTGGACCATCTTC	55159
rs762890817	snp	A/G	2.30439e-05	0.00339432	intron-variant	RFWD3	GRCh38.p7	16:74624121	CAGTCAGTACACGAA[A/G]GGACTTCCATTCTTC	55159
rs762898746	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668866	AAAGATATATGAATG[G/T]ACTTTATTAAAATGT	55159
rs762914601	in-del	-/CT			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663830	TTATTGAGAAGCAAG[-/CT]CTGATTCCCACTAAA	55159
rs762933075	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74642623	CTCTCTCCTGAGTAG[C/G]TGAGACTACAGGTGT	55159
rs763035630	snp	C/G	3.29832e-05	0.00406085	missense	RFWD3	GRCh38.p7	16:74632627	ATGCATCGGAATGTA[C/G]TGACTGCTCTTCATG	55159
rs763042539	in-del	-/TTAG			intron-variant	RFWD3	GRCh38.p7	16:74635685	CTTTTTATTAAAAAC[-/TTAG]TTAGATGGGATAAAG	55159
rs763045391	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629688	AAAAACCTTGCCATA[C/T]TTTACTGTCTACTCT	55159
rs763223728	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74651295	GTCAGCCTAGACAGG[G/T]TGCTGAATTTACAAA	55159
rs763234685	snp	G/T	4.94173e-05	0.00497053	synonymous-codon	RFWD3	GRCh38.p7	16:74661054	CAGGAATTCCAGCAT[G/T]CCATGAAGTCTCTGC	55159
rs763237873	snp	C/T	3.29451e-05	0.00405851	missense	RFWD3	GRCh38.p7	16:74626386	GTACACACCAGGATG[C/T]TGCCATCATTCTCTG	55159
rs763312081	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622440	GACCAGCCTGGACAA[C/T]GTAGTGAAACATCTA	55159
rs763320466	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74658221	GGAAAACAATATTGT[C/G]ATCTGTGTTATTCAC	55159
rs763326198	snp	A/C	1.6486e-05	0.00287102	synonymous-codon	RFWD3	GRCh38.p7	16:74660973	TCCGGCTCTTGCCCT[A/C]CGTGAAGCAGATACC	55159
rs763347252	in-del	-/CTCCATCGATACATGTAA	1.64785e-05	0.00287037	cds-indel	RFWD3	GRCh38.p7	16:74649152	TGGGGAGGGTCTTGC[-/CTCCATCGATACATGTAA]CTTCTTGCTCTGCTG	55159
rs763354295	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646025	AGTGCAGGGATTACA[A/G]ACGTGAGCCACCATG	55159
rs763417863	snp	C/T	1.6476e-05	0.00287014	missense	RFWD3	GRCh38.p7	16:74644602	CTATACCCAAAGAGA[C/T]GCCCACAGCGTAATG	55159
rs763421582	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630517	GCTGGGTTCTGAATA[C/T]AGATCTGACTCTATT	55159
rs763505418	snp	C/T	3.29484e-05	0.00405871	intron-variant	RFWD3	GRCh38.p7	16:74644486	ACATAATTAGAGTGG[C/T]TCTAGGAATCTGCCT	55159
rs763507692	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621618	CAGAGACTGGTGGAG[C/T]CCAGAAGACTAAAGC	55159
rs763583923	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74644041	CTGCATGTGCAAAGC[A/T]TCACTTATGAGTTTT	55159
rs763643624	snp	C/G/T	4.9429e-05	0.00497116	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74636518	GCTCAGGACCCATGC[C/G/T]TGGGAGCCCCTGGGT	55159
rs763650233	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624556	ATCCACCACCACGCC[C/T]GGCTAATTTTCTTGT	55159
rs763650442	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74635264	GTCCGGCCTAGGCGA[A/T]AGAGCGAGACTCCAT	55159
rs763663755	snp	A/G	1.66346e-05	0.00288393	intron-variant	RFWD3	GRCh38.p7	16:74651880	ATTTAAGCTTCATGG[A/G]TGTTAGCCTTGTGAG	55159
rs763676630	snp	C/G/T	1.64844e-05	0.00287087	missense	RFWD3	GRCh38.p7	16:74660974	CCGGCTCTTGCCCTC[C/G/T]GTGAAGCAGATACCC	55159
rs763681358	snp	G/T	1.65482e-05	0.00287643	synonymous-codon	RFWD3	GRCh38.p7	16:74628458	ACTACTTACCAGGCC[G/T]GTAGGTCACAAGACA	55159
rs763731556	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74656067	AAGACTTATTATTTA[A/G]GAAATAAGGCCAGAC	55159
rs763826550	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644815	CAACTAAGAAATTAA[C/T]AGAAGTGCAAAAAAA	55159
rs763874688	snp	A/G	3.29462e-05	0.00405857	missense	RFWD3	GRCh38.p7	16:74661007	CTTCTTGTTCTCATT[A/G]GCCCTACACTGTGGT	55159
rs763875920	snp	A/C/G	6.59918e-05	0.00574388	missense	RFWD3	GRCh38.p7	16:74628589	GAAGCATCCTCCAAG[A/C/G]TTCCAGCCAGCACCC	55159
rs763914616	snp	A/T	2.63265e-05	0.00362803	intron-variant	RFWD3	GRCh38.p7	16:74649092	CTCTAAAAATAAATA[A/T]ATAAATAAATAGATT	55159
rs763922576	snp	A/G			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662040	TTCCATCATGTTAGC[A/G]TATTCAACAAATATT	55159
rs763928776	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74644820	AAGAAATTAACAGAA[G/T]TGCAAAAAAAATGAT	55159
rs763982760	snp	C/G	1.6703e-05	0.00288985	missense	RFWD3	GRCh38.p7	16:74624030	CACAGGCTGATCGGT[C/G]TGTAGGTCCTGGAGC	55159
rs764008429	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629901	ACATTCTAAGACAGA[A/G]TGGTGCTGGTGGCCA	55159
rs764022075	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625078	GGTGGCACACACCCA[C/T]AGTTCCAGCTACTTG	55159
rs764045467	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74641508	AATATTATCAAGAAA[C/T]TGAAATGAAAAAAAC	55159
rs764046041	snp	A/T	3.295e-05	0.00405881	missense	RFWD3	GRCh38.p7	16:74651996	GCTGTCACTGTCAGA[A/T]TCAGAACTACTAGAC	55159
rs764074597	snp	G/T	4.94173e-05	0.00497053	missense	RFWD3	GRCh38.p7	16:74626387	TACACACCAGGATGT[G/T]GCCATCATTCTCTGG	55159
rs764091102	snp	A/G	1.64966e-05	0.00287194	synonymous-codon	RFWD3	GRCh38.p7	16:74632633	CGGAATGTACTGACT[A/G]CTCTTCATGTTGGCA	55159
rs764132999	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648528	CTATAATCCCAGCAC[C/T]TTGGGAGGCCGAGGT	55159
rs764140674	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668408	CAACTACACCAACAA[A/G]AATTAGTGCTAGTTG	55159
rs764171193	snp	C/T	1.79974e-05	0.00299973	missense	RFWD3	GRCh38.p7	16:74637857	AAGGACAAACGTACC[C/T]GAACACGCCTTTGAA	55159
rs764181044	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623534	ATACTTAAGTGACAG[C/G]ACAACTCAGATGGGA	55159
rs764209847	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74629582	CAGTGATCCAAGACT[-/G]TGCCACTGCACTCCA	55159
rs764224311	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622985	TGTTTTCAATAGCAG[C/T]CTGAATAGCTTTTGT	55159
rs764224907	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74649580	AAAAACTTCTGCAAC[A/T]CTGATAAGAATTCTT	55159
rs764239435	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74658513	AGTAAATGTCAAACA[A/C]CACACTGAGAAATTC	55159
rs764301479	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74648760	ACCCTGGGCAACAGA[G/T]TGAGACTCCGTCTCA	55159
rs764314777	in-del	-/GTT/TC			intron-variant	RFWD3	GRCh38.p7	16:74657477	CCAGGTTTTCTTTTT[-/GTT/TC]CTTTTTTTTTTTTTT	55159
rs764322759	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74628781	GGTTAAACGCCTTTA[A/G]TCACTATCCTCTGAT	55159
rs764326136	snp	A/T	1.65127e-05	0.00287334	missense	RFWD3	GRCh38.p7	16:74652078	GCTGGCAAGTCAGGC[A/T]GGGTCCTGCTCACCT	55159
rs764329207	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647434	CTGGGACTATAGGCA[C/T]GCACCACCATATCCG	55159
rs764415796	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74666671	CGGGTTCCAAGCCCG[C/G]GTGCAGCCCACCTCG	55159
rs764419342	snp	G/T	8.23662e-05	0.00641688	intron-variant	RFWD3	GRCh38.p7	16:74644492	TTAGAGTGGTTCTAG[G/T]AATCTGCCTGACTTA	55159
rs764425652	in-del	-/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668832	TCAATAAACGTAGTA[-/T]TCCATTGGAAAGCAA	55159
rs764505318	snp	A/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644387	GCTCCTGTTCACTAG[A/T]GTCCAAAGCTCTCAG	55159
rs764506999	snp	G/T	4.94181e-05	0.00497057	synonymous-codon	RFWD3	GRCh38.p7	16:74661065	GCATGCCATGAAGTC[G/T]CTGCAGTCCGCTGAT	55159
rs764518765	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638420	CAAAGGAAAGACCAA[C/T]TAGAATTAAGGAAAA	55159
rs764560251	in-del	-/CTAC	1.79832e-05	0.00299854	intron-variant	RFWD3	GRCh38.p7	16:74630747	GCCAAGAGAAAGCTG[-/CTAC]CTACCACCAGGAAAA	55159
rs764607071	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636736	TTTTTTTTTTTAAGA[C/T]GGAGTCTCACTCTGT	55159
rs764618501	snp	C/T	1.6483e-05	0.00287076	missense	RFWD3	GRCh38.p7	16:74632539	TGGTCAGTTTAATAG[C/T]GTTGTCTAGGGAAGC	55159
rs764633585	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74638192	TAGAAAATGGGGACT[-/A]AAAATGCCACAGGCA	55159
rs764648343	in-del	-/TT	4.9509e-05	0.00497514	intron-variant	RFWD3	GRCh38.p7	16:74636341	TGAGGTTCTAGACTC[-/TT]TACCTGGAAGAAAAG	55159
rs764674548	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627793	TGAACACCCACAACG[A/G]ACTCCCTAGTGTTTG	55159
rs764706461	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74626055	GTCGGGCATGGTGGT[A/G]GGGTGCCTGTAATCC	55159
rs764714348	snp	C/G/T			intron-variant	RFWD3	GRCh38.p7	16:74665396	CAGAATGGCCAATAT[C/G/T]GTGAAACCCCGTCTC	55159
rs764812877	snp	A/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662216	GAATGCCTGGCCTTA[A/C]CTCCTCATGCATCAG	55159
rs764816178	snp	C/G/T	4.98263e-05	0.0049911	intron-variant	RFWD3	GRCh38.p7	16:74636317	GAGTCTAATAAAGAA[C/G/T]ATGAAAGCTGAGGTT	55159
rs764870539	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74636969	CCACCCGCCTCGGCC[A/G]CCCAAAGTGCTGGGA	55159
rs764903046	snp	A/C/G/T	4.95311e-05	0.00497631	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74626525	AGGACATTTCCATCA[A/C/G/T]CACACTTCGTATGGT	55159
rs764904256	snp	C/T	1.7031e-05	0.00291808	intron-variant	RFWD3	GRCh38.p7	16:74644757	GGAAAGCAGAATATA[C/T]TCAAATTAGAGAAAA	55159
rs764954139	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74635354	CACCCGTAGTCTCAA[A/C]TACTTGGGAGGCTGA	55159
rs765002819	snp	A/G	1.64898e-05	0.00287135	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630834	CGTGTTTCGCACGTC[A/G]TATACCAGAATTGAA	55159
rs765013727	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74652756	TTTAAAATAACCACT[A/G]CTGTACCTCAGTTTC	55159
rs765021943	snp	C/G	4.94776e-05	0.00497357	missense	RFWD3	GRCh38.p7	16:74661287	CCTCAGCAGGAGCTG[C/G]CTGGAGGATGGATGG	55159
rs765072445	in-del	-/AAGT			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662316	CTTAATTACTTTGTG[-/AAGT]AAGGCACGTGCTTTT	55159
rs765081460	snp	A/G	1.69763e-05	0.0029134	stop-gained	RFWD3	GRCh38.p7	16:74637912	CCTGCAGTTGGAGTC[A/G]GCACTGTGCTGATTC	55159
rs765096630	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74646279	TAGTCAGGAGGCTGA[-/G]GTAGAAGCATCACCT	55159
rs765177927	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74631726	AGACCAGGACCAGGA[A/G]TAAACAGTACCAACC	55159
rs765216000	snp	C/T	1.64944e-05	0.00287175	missense	RFWD3	GRCh38.p7	16:74632524	CCCAAATCACTCACC[C/T]GGTCAGTTTAATAGT	55159
rs765234319	snp	C/T	1.64741e-05	0.00286998	intron-variant	RFWD3	GRCh38.p7	16:74644478	CCAATAGGACATAAT[C/T]AGAGTGGTTCTAGGA	55159
rs765255045	snp	C/T	4.94197e-05	0.00497066	synonymous-codon	RFWD3	GRCh38.p7	16:74661207	CAAGACCTCCACTTC[C/T]GTCAGGTCAACAGAC	55159
rs765268288	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74638526	ATGTACCTAAAAACA[C/G]TCTCAAAATATGAAA	55159
rs765312541	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74659589	GACAGAGCAAGACTC[-/TT]GTCTTAAAAACAAAA	55159
rs765354613	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74628960	ATGAAGCTTGACTGA[C/T]GTGAAGCTTCTGGAA	55159
rs765365526	snp	A/G	1.65707e-05	0.00287838	intron-variant	RFWD3	GRCh38.p7	16:74632479	ATTCCATGCTACTCA[A/G]CACCAAAGAGCCCAG	55159
rs765389214	snp	A/C	9.9453e-05	0.007051	intron-variant	RFWD3	GRCh38.p7	16:74651900	AGCCTTGTGAGTCCA[A/C]ACCTGGGTAAAATAC	55159
rs765394837	snp	C/G	3.43784e-05	0.00414585	missense	RFWD3	GRCh38.p7	16:74624058	AGCAACGAGCCACTG[C/G]CAGCATCCCACAGCT	55159
rs765411085	snp	A/G	3.56958e-05	0.00422453	intron-variant	RFWD3	GRCh38.p7	16:74661463	ATCACTAGAGAAACA[A/G]TATTTGTAAAAAGTA	55159
rs765432321	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648697	GAATTGCTTAAACAC[A/G]GGAGGCAGAGGTTAT	55159
rs765483127	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74630528	ATATAGATCTGACTC[-/T]TATTTTGCCATGTTA	55159
rs765496716	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74644982	TTTCCTTCACTCAAA[C/G]GAAGAAAAGCAGCTA	55159
rs765500298	in-del	-/TAG			intron-variant	RFWD3	GRCh38.p7	16:74666215	AGATAGATAGATAGA[-/TAG]ATAGATTGATTAGAT	55159
rs765527820	in-del	-/T	1.68464e-05	0.00290222	frameshift-variant	RFWD3	GRCh38.p7	16:74636561	GACTTTGATGTGACG[-/T]TAAGTTTTTGCAAGT	55159
rs765531645	snp	C/G	1.66153e-05	0.00288225	intron-variant	RFWD3	GRCh38.p7	16:74628438	AAGCTATGGGAGACC[C/G]CAGCACTACTTACCA	55159
rs765559118	snp	G/T	0.000313834	0.0125227	synonymous-codon	RFWD3	GRCh38.p7	16:74660958	TGTCCTCTGAGACCC[G/T]CCGGCTCTTGCCCTC	55159
rs765564931	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666983	TCTTCTTCAATGGGT[A/C]CCCCGATAGCTGAAG	55159
rs765595626	snp	C/T	4.47157e-05	0.0047282	intron-variant	RFWD3	GRCh38.p7	16:74624117	GAGTCAGTCAGTACA[C/T]GAAGGGACTTCCATT	55159
rs765674281	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74657338	ACTCCCTGGATTGCT[A/G]TAAGCATTTGGTCAG	55159
rs765729793	in-del	-/A	1.7293e-05	0.00294044	intron-variant	RFWD3	GRCh38.p7	16:74649112	TAAATAGATTTTTTT[-/A]AAAATGATGTTCATA	55159
rs765741447	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629551	ATAGTCCCAGCTACT[C/T]GGGAGGTGGAGGATG	55159
rs765756252	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665524	CAGAGGTTGCAGTGA[C/G]CCGAGATCGCACCAC	55159
rs765759290	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627596	CCTAACTTGTTTCCT[A/G]GTCAGGGCTCTTCTA	55159
rs765762248	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74645989	TCCTGACCTCGCGAT[A/C]CGTCCGCCTTGGCCT	55159
rs765781494	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621881	TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC	55159
rs765843634	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663441	GGGGGAAGAACGGCC[A/G]CTAGATTTGGCAACA	55159
rs765853617	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74653632	AGACTAGCCAACAAA[C/G]TAAGACACCATCTCT	55159
rs765886734	snp	A/C/G/T	8.24836e-05	0.00642151	missense, intron-variant	RFWD3	GRCh38.p7	16:74630830	TGCTCGTGTTTCGCA[A/C/G/T]GTCATATACCAGAAT	55159
rs765904014	snp	A/C/G	3.3719e-05	0.00410592	intron-variant	RFWD3	GRCh38.p7	16:74644746	GATGGCTAGATGGAA[A/C/G]GCAGAATATATTCAA	55159
rs765959834	snp	C/G	1.64833e-05	0.00287078	missense	RFWD3	GRCh38.p7	16:74661267	TGTCGCTTGGCTGCT[C/G]ATCACCTCAGCAGGA	55159
rs766162298	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632838	ATTTATTCATTTATT[C/T]TTGAGAGTTGGCCAG	55159
rs766181349	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659381	TGCCTTCACCTATAA[C/T]ACAAATGTATGAAAT	55159
rs766193206	in-del	-/CAA			intron-variant	RFWD3	GRCh38.p7	16:74646913	CCGTCTCAACAACAA[-/CAA]CAACAACAACAACAA	55159
rs766203008	in-del	-/CTG	3.29511e-05	0.00405887	cds-indel	RFWD3	GRCh38.p7	16:74649179	ATGTAACTTCTTGCT[-/CTG]CTGAGACACCTGCTA	55159
rs766228902	snp	C/T	3.29783e-05	0.00406055	missense	RFWD3	GRCh38.p7	16:74636549	TGCTGTAAATTCTGA[C/T]TTTGATGTGACGTAA	55159
rs766250216	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657598	CTCCTGCCTCAGTCT[C/T]CTGAGCAGCTGGGAT	55159
rs766322583	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74627178	ACTTAAAAACATGAG[G/T]AGACCCACCCACAAC	55159
rs766329508	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74665593	AAAAAAAGAAAGAAA[A/T]AAGAAAAATAAAACA	55159
rs766329644	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623661	AATAAGAATTTCCAA[C/T]ATACAATAATGGTTA	55159
rs766354757	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643830	ACAGGCGTCCGCCAC[C/T]ATGCCCGGCTAATTT	55159
rs766471769	in-del	-/TT/TTT			intron-variant	RFWD3	GRCh38.p7	16:74657478	CAGGTTTTCTTTTTC[-/TT/TTT]TTTTTTTTTTTTTTT	55159
rs766511277	in-del	-/TC			frameshift-variant	RFWD3	GRCh38.p7	16:74661205	CCCAAGACCTCCACT[-/TC]TGTCAGGTCAACAGA	55159
rs766549433	snp	A/G	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644368	ACCACCTACCTTTTC[A/G]TGCGCTCCTGTTCAC	55159
rs766549483	snp	C/T	1.65411e-05	0.00287581	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630939	ATTATAAGTCTGGAC[C/T]ACGGTATTTGTCTCC	55159
rs766622407	in-del	-/TAGATAGATAGA			intron-variant	RFWD3	GRCh38.p7	16:74666183	ATTAGATAGACAGAT[-/TAGATAGATAGA]TAGATAGATAGATAG	55159
rs766633525	snp	A/G	2.58241e-05	0.00359324	intron-variant	RFWD3	GRCh38.p7	16:74637994	GGAAAGCCAGCAACA[A/G]GTGGGGATTAGGAAG	55159
rs766637101	snp	A/C/T			intron-variant	RFWD3	GRCh38.p7	16:74666473	CTCTCGGGGGAAGGG[A/C/T]CGGGCGACCTCCCAC	55159
rs766658885	snp	A/C/G	3.32968e-05	0.00408014	intron-variant	RFWD3	GRCh38.p7	16:74636311	TATATGGAGTCTAAT[A/C/G]AAGAACATGAAAGCT	55159
rs766670096	snp	C/T	1.76145e-05	0.00296765	intron-variant	RFWD3	GRCh38.p7	16:74631008	AGAAAATCAAATACA[C/T]GACAAAGATGTAAAG	55159
rs766717916	snp	A/G	1.64806e-05	0.00287054	synonymous-codon	RFWD3	GRCh38.p7	16:74626508	AGTGTCATCCAGTCG[A/G]TAGGACATTTCCATC	55159
rs766822467	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635563	AGCACACTATCAAGC[A/G]GACTGGAATGGACAC	55159
rs766827430	snp	A/G	1.65348e-05	0.00287526	missense	RFWD3	GRCh38.p7	16:74652097	TCCTGCTCACCTGAA[A/G]GTAAGCATCCAATGG	55159
rs766830717	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632165	GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTCAG	55159
rs766837271	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74651274	ATTATACTAGGACTT[G/T]AAAGTGTCAGCCTAG	55159
rs766853659	snp	A/G	1.779e-05	0.00298239	intron-variant	RFWD3	GRCh38.p7	16:74660882	CAGAGCCTCAGTTTC[A/G]TAATTTCTAGTACAG	55159
rs766866747	snp	A/C			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621627	GTGGAGCCCAGAAGA[A/C]TAAAGCCTGGATTTA	55159
rs766893200	in-del	-/TACAAAATGCCAC			intron-variant	RFWD3	GRCh38.p7	16:74651679	AGAAGTGAAAGAGAA[-/TACAAAATGCCAC]TACAAAGTGACTAAC	55159
rs766912077	snp	A/T	1.66957e-05	0.00288922	intron-variant	RFWD3	GRCh38.p7	16:74628422	CACTGTGCTCCCAAA[A/T]AAGCTATGGGAGACC	55159
rs766943919	snp	C/T	1.65272e-05	0.0028746	missense	RFWD3	GRCh38.p7	16:74628629	GAAATGCAGCTGAGG[C/T]AGCTCTGGGCATGTA	55159
rs767019872	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74661170	AAGTTCTTGGATTGA[C/T]GTTCTCCACAGTGTC	55159
rs767043799	snp	A/G	1.68527e-05	0.00290277	intron-variant	RFWD3	GRCh38.p7	16:74628714	CTCCAAAACTCGGAC[A/G]GCTCCAGACCCCACT	55159
rs767059852	snp	C/T	2.30508e-05	0.00339483	intron-variant	RFWD3	GRCh38.p7	16:74637813	TAGCTTCCTCTTCCA[C/T]TCCTATTCCAAAAGT	55159
rs767091678	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74653820	GCTGCAATTTATTGA[G/T]GAATTAGGGCTTTGA	55159
rs767119407	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664629	TGGTGTGCACCTGTG[A/G]TCCTAGCTACTTGGG	55159
rs767166123	in-del	-/CATAT	1.74615e-05	0.00295473	intron-variant	RFWD3	GRCh38.p7	16:74660917	GATCACAGACTTATC[-/CATAT]ATTTATTTACCTGGC	55159
rs767181706	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654904	CAACTCTCTTTAATT[C/T]TGTGAAAGCTGAGAA	55159
rs767211022	snp	G/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623452	CTCTTGTGTTCAACT[G/T]AATAATACTCTTTTA	55159
rs767271502	snp	C/G	1.66308e-05	0.00288359	intron-variant	RFWD3	GRCh38.p7	16:74651886	GCTTCATGGATGTTA[C/G]CCTTGTGAGTCCAAA	55159
rs767282404	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668516	CATATGTTCCTAAGT[A/G]TGTTCCCTTGGCAGA	55159
rs767285351	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659519	AGAATCGCTTGAACC[C/T]GGGAGCCAGAGGTCC	55159
rs767285513	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74651340	TAAAGAATCTAGGCC[A/G]GGTGCAGTGGCTCAT	55159
rs767294942	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74624526	TCAGCCTCCCAAGTA[C/G]CTGGGATTACAGACA	55159
rs767312037	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	RFWD3	GRCh38.p7	16:74636521	CAGGACCCATGCTTG[A/G]GAGCCCCTGGGTTGC	55159
rs767323644	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660677	TTGGTGTACAAGACA[C/T]AATCTGAACAACAGC	55159
rs767359427	snp	C/T	1.70174e-05	0.00291692	missense	RFWD3	GRCh38.p7	16:74661437	CATCATATTCCATTG[C/T]TTCATGAGCCATCAC	55159
rs767360542	snp	A/C	1.7122e-05	0.00292587	missense	RFWD3	GRCh38.p7	16:74624045	CTGTAGGTCCTGGAG[A/C]AACGAGCCACTGGCA	55159
rs767361315	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623849	CTGCAGACAATAAAC[A/G]GGGATCTTGCTTGGG	55159
rs767417582	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74638709	ATTAGATCAACAGCA[C/G]TCCTCATCAGATAAC	55159
rs767495570	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634225	CAAGATATGTCACAT[C/T]TGTCTGAAATGAAAT	55159
rs767500040	in-del	-/AGT	3.31851e-05	0.00407326	intron-variant	RFWD3	GRCh38.p7	16:74628677	GGCATCTGAAAGGAA[-/AGT]AAGGAAACTGTATCT	55159
rs767595175	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74660048	GAGCACAGTGAGACC[C/G]TGTCTCAAAAATAAC	55159
rs767600574	snp	A/G	1.6477e-05	0.00287024	synonymous-codon	RFWD3	GRCh38.p7	16:74626496	GATTGGATTTCCAGT[A/G]TCATCCAGTCGGTAG	55159
rs767651180	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663929	AAAAGCCAGTAAAGC[A/G]GTTAGCTTGACTCCT	55159
rs767667441	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657564	CACTGCAACATCCAC[C/T]TCCCGGGTTCAAGCG	55159
rs767682906	snp	C/G	3.51093e-05	0.00418968	intron-variant	RFWD3	GRCh38.p7	16:74652160	GAATTATAGTACAAT[C/G]AACTATCATCACAAA	55159
rs767683465	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622765	GGCAAAGTAGTCTGA[A/G]GCAAGGCAAAGAAAT	55159
rs767696334	in-del	-/ATTA			intron-variant	RFWD3	GRCh38.p7	16:74641469	GCCTGGCCTAAACAG[-/ATTA]ATTAATTTTGACTAG	55159
rs767697718	in-del	-/AGATAGA			intron-variant	RFWD3	GRCh38.p7	16:74666208	GATAGATAGATAGAT[-/AGATAGA]TAGATAGATTGATTA	55159
rs767770844	snp	C/T	1.65217e-05	0.00287412	missense	RFWD3	GRCh38.p7	16:74652088	CAGGCTGGGTCCTGC[C/T]CACCTGAAAGTAAGC	55159
rs767805716	snp	A/G	2.49741e-05	0.00353361	intron-variant	RFWD3	GRCh38.p7	16:74637991	GGGGGAAAGCCAGCA[A/G]CAAGTGGGGATTAGG	55159
rs767869165	snp	G/T	3.29549e-05	0.00405911	synonymous-codon	RFWD3	GRCh38.p7	16:74632549	AATAGTGTTGTCTAG[G/T]GAAGCAGAGAGTAGC	55159
rs767921587	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663536	TGCAGGCTGAATAAA[C/T]GGAAGGAATTCTAAT	55159
rs767975416	snp	C/T	3.33634e-05	0.00408418	intron-variant	RFWD3	GRCh38.p7	16:74636298	GCAAGGAAATAAATA[C/T]ATGGAGTCTAATAAA	55159
rs767977113	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74626414	CTGGGCTTTGGAAAA[C/T]GGCATTTTTGGTCAA	55159
rs767986935	snp	C/G	3.29506e-05	0.00405884	intron-variant	RFWD3	GRCh38.p7	16:74626334	AAAGTAAAAAAGTAA[C/G]AGGCTCACCAGGGCA	55159
rs768015762	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645948	AGAGACGGGGTTTCA[C/T]CGTGTTAGTTAGGAT	55159
rs768051478	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74627763	ACAGAGGAGTATCCT[C/G]TGAAAGGCAAACTAT	55159
rs768103820	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74639039	ATTGAGCTAAGACTT[-/TT]TTTTTTTTTTTTTTT	55159
rs768237871	snp	C/T	1.98352e-05	0.00314916	intron-variant	RFWD3	GRCh38.p7	16:74624105	GGGAAGGGTCAGGAG[C/T]CAGTCAGTACACGAA	55159
rs768270631	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646700	CTGAGGCAGGGGAAT[C/T]GCTTGAACTCAGGAG	55159
rs768278697	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74665753	TTCTTTCTTTCTTTC[-/T]TTCTTTTTTTGAGAT	55159
rs768315407	snp	C/G	1.64795e-05	0.00287045	missense	RFWD3	GRCh38.p7	16:74652025	ACACCTGCAACTCTT[C/G]AGATACAGGATTCCT	55159
rs768388347	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74626019	GGTGAAACCCTGTCT[C/G]TACTAAAAATACAAA	55159
rs768389154	in-del	-/TAGA			intron-variant	RFWD3	GRCh38.p7	16:74666191	GACAGATTAGATAGA[-/TAGA]TAGATAGATAGATAG	55159
rs768475904	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74627072	GTACACCAGTCACAA[C/G]AAATCACAGTCTTGG	55159
rs768531617	snp	A/C	1.67649e-05	0.0028952	missense	RFWD3	GRCh38.p7	16:74661416	CATGATTTAACTGCA[A/C]CTGAACATCATATTC	55159
rs768574968	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664095	AGAAAGTCTGCAAAC[C/T]GAACAATGTGAGATA	55159
rs768578105	snp	A/C/T	3.29464e-05	0.00405861	missense	RFWD3	GRCh38.p7	16:74644362	ACTCTTACCACCTAC[A/C/T]TTTTCATGCGCTCCT	55159
rs768578268	snp	A/T	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74661004	CTCCTTCTTGTTCTC[A/T]TTGGCCCTACACTGT	55159
rs768637413	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74653406	GGATCACTTGAGCCC[A/G]AGAGTTTGAGGCCAC	55159
rs768649988	in-del	-/AC			intron-variant	RFWD3	GRCh38.p7	16:74633656	AACTTTTGCGGTAAT[-/AC]ATATGTTCATGGCCA	55159
rs768672277	in-del	-/G	3.29674e-05	0.00405988	intron-variant	RFWD3	GRCh38.p7	16:74626330	TATGAAAGTAAAAAA[-/G]TAACAGGCTCACCAG	55159
rs768683544	snp	C/T	3.30819e-05	0.00406692	intron-variant	RFWD3	GRCh38.p7	16:74632501	AGAGCCCAGTCTCCA[C/T]CTACTTCCCCAAATC	55159
rs768715806	snp	A/C	1.77168e-05	0.00297626	intron-variant	RFWD3	GRCh38.p7	16:74632710	GAAATAGATCACTGA[A/C]AGTGAACCTAGGGCA	55159
rs768734363	snp	C/T	1.66073e-05	0.00288156	missense	RFWD3	GRCh38.p7	16:74644725	AGAGGCTCAGACTTC[C/T]GGGGAGATGGCTAGA	55159
rs768751163	snp	A/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668846	ATTCCATTGGAAAGC[A/T]AACAAAAGATATATG	55159
rs768764466	in-del	-/GTCTCC	1.65712e-05	0.00287843	intron-variant	RFWD3	GRCh38.p7	16:74632478	ATTCCATGCTACTCA[-/GTCTCC]ACACCAAAGAGCCCA	55159
rs768789432	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74660531	CCCTGTCAAGACTTG[A/T]CAGCTAAGCCCTTCA	55159
rs768821908	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622945	TTAGATAGGAACTCT[C/T]AAAATGGGAGACAAG	55159
rs768901115	snp	A/G/T			intron-variant	RFWD3	GRCh38.p7	16:74624356	TCTAGGGACAGAAGG[A/G/T]TCAATAAGATAAAGT	55159
rs768929061	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74644393	GTTCACTAGTGTCCA[A/G]AGCTCTCAGGGTTCG	55159
rs768967844	snp	C/T	3.29489e-05	0.00405874	missense	RFWD3	GRCh38.p7	16:74626483	GCTGGCAGGAGCAGA[C/T]TGGATTTCCAGTGTC	55159
rs768970320	in-del	-/T	0.000613062	0.0174973	intron-variant	RFWD3	GRCh38.p7	16:74649101	AAATAAATAAATAAA[-/T]TAGATTTTTTTAAAA	55159
rs768985450	snp	C/T	4.94181e-05	0.00497057	missense	RFWD3	GRCh38.p7	16:74661166	TCTGAAGTTCTTGGA[C/T]TGATGTTCTCCACAG	55159
rs769001463	snp	C/G/T	3.29669e-05	0.00405984	synonymous-codon	RFWD3	GRCh38.p7	16:74632618	CTGTTTGCCATGCAT[C/G/T]GGAATGTACTGACTG	55159
rs769021043	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74639381	CACTTACGCAACAGA[A/C]TTTTCAGCTCCATTA	55159
rs769080008	snp	A/G	1.69789e-05	0.00291362	missense	RFWD3	GRCh38.p7	16:74637882	TTTGAAGCCTAGTGC[A/G]CTTATCAGTGAGGAC	55159
rs769108859	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74629413	CCTGTAATCCCAGCA[C/T]TTCGGGAAGCCGAGG	55159
rs769112045	snp	A/C/T	4.94273e-05	0.00497108	synonymous-codon	RFWD3	GRCh38.p7	16:74644604	ATACCCAAAGAGATG[A/C/T]CCACAGCGTAATGCT	55159
rs769140398	snp	A/G	1.65663e-05	0.002878	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630810	TACTAACTCCTGCAC[A/G]TGACTGCTCGTGTTT	55159
rs769149873	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74636101	GTAACCTACACTTCC[A/G]AGGACCTCACCATCT	55159
rs769162333	snp	C/T	1.67172e-05	0.00289108	missense	RFWD3	GRCh38.p7	16:74661403	GGCTGTTGTTCGGCA[C/T]GATTTAACTGCACCT	55159
rs769224541	snp	A/G	1.66349e-05	0.00288395	synonymous-codon	RFWD3	GRCh38.p7	16:74624024	GTCCAACACAGGCTG[A/G]TCGGTCTGTAGGTCC	55159
rs769224672	snp	C/T	1.6566e-05	0.00287797	intron-variant	RFWD3	GRCh38.p7	16:74632490	CTCAACACCAAAGAG[C/T]CCAGTCTCCACCTAC	55159
rs769319764	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622363	GGTGCAGTGGCTCAC[A/G]CCTATAATTTTGGCA	55159
rs769389931	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74647681	ACTGCAACTTCTGCC[G/T]CCCAGGTTCAAGCGA	55159
rs769409271	snp	G/T	1.66076e-05	0.00288158	missense	RFWD3	GRCh38.p7	16:74661352	GGCTGGAGGAGGGCT[G/T]GTCCCCCTTGGCTGC	55159
rs769420079	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74628101	GCCTTTCTCTCAGGG[G/T]AAGTAAGAGGCAGGC	55159
rs769455550	in-del	-/T/TAGC			intron-variant	RFWD3	GRCh38.p7	16:74666218	AGATAGATAGATAGA[-/T/TAGC]TAGATTGATTAGATA	55159
rs769462918	in-del	-/C	1.6525e-05	0.00287441	intron-variant	RFWD3	GRCh38.p7	16:74632507	AGTCTCCACCTACTT[-/C]CCCCAAATCACTCAC	55159
rs769463980	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650050	AGCCCTGGGCAACCA[C/T]TAATATTATCTCTGT	55159
rs769479301	snp	A/G	6.94444e-05	0.00589215	intron-variant	RFWD3	GRCh38.p7	16:74652153	GACAACGGAATTATA[A/G]TACAATGAACTATCA	55159
rs769526949	snp	C/T	1.64914e-05	0.00287149	intron-variant	RFWD3	GRCh38.p7	16:74649248	AGGTAAAATACAAAA[C/T]AAGATATGTCAGGTA	55159
rs769550698	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74648015	GCAGTGGTGCAATCA[C/T]GGCTCACTGAAGCCT	55159
rs769615810	snp	A/G	1.71971e-05	0.00293227	intron-variant	RFWD3	GRCh38.p7	16:74660926	CTTATCCATATATTT[A/G]TTTACCTGGCACTGT	55159
rs769631256	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667948	GCTAAACAGGGGAGT[A/G]AAGACTCCAGTAACC	55159
rs769689219	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74655681	CTGCAGTGCAGTGGC[A/G]CCTGGCTAATTTGTT	55159
rs769750380	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74664956	GGAGGTGCCTAGAAC[A/G]AGAGACCATGGGCTG	55159
rs769808788	snp	C/T	1.64738e-05	0.00286995	intron-variant	RFWD3	GRCh38.p7	16:74644336	CAAAAGGGAACATTC[C/T]AGCCAGGCATACTCT	55159
rs769823837	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74652155	CAACGGAATTATAGT[A/T]CAATGAACTATCATC	55159
rs769865768	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74661144	ATCAGATCCCTGCCT[A/G]TGTTGTTCTGAAGTT	55159
rs769888434	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74651159	TATACTGAAAGAGCG[C/T]CCTCTGGGGATCAGA	55159
rs769900608	snp	G/T	1.64741e-05	0.00286998	missense	RFWD3	GRCh38.p7	16:74644578	CCTTTAAGCCACGTG[G/T]AAATGCACCTATACC	55159
rs769938710	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74661689	AAAACATGAAGTCCT[A/G]TGATCATAGTAGTAT	55159
rs769938932	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74624836	ATCCAATCTCTACAA[G/T]AAAAAATTAGCCAGG	55159
rs769948841	snp	C/G	4.9717e-05	0.00498558	synonymous-codon	RFWD3	GRCh38.p7	16:74644709	AGAAGCAGAAGGTAG[C/G]AGAGGCTCAGACTTC	55159
rs769984267	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74633677	GTTCATGGCCAAGCA[C/T]GGTAGCTCGCGCCTG	55159
rs769986218	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74654404	TGTTATGTAATTTTT[A/G]CAAGTTTGGTGTGCA	55159
rs770024280	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74666285	GAAACTTTGGGCGGG[C/T]TTCCTAAACTCGGCT	55159
rs770094777	snp	C/G/T	9.89126e-05	0.0070319	missense	RFWD3	GRCh38.p7	16:74632623	TGCCATGCATCGGAA[C/G/T]GTACTGACTGCTCTT	55159
rs770142776	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623039	TGATCTCTGACACTA[C/G]GGGAGACTCAAGTAA	55159
rs770231910	snp	C/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621335	GGATTATATCCCTCT[C/T]CCAAGAGGCAGACAT	55159
rs770249929	snp	C/T	1.66369e-05	0.00288412	intron-variant	RFWD3	GRCh38.p7	16:74628695	AAGGAAACTGTATCT[C/T]ACACTCCAAAACTCG	55159
rs770275165	snp	A/G	2.22289e-05	0.00333376	intron-variant	RFWD3	GRCh38.p7	16:74636590	GTCCTAAAATGAAAA[A/G]GATTTTATAAATACA	55159
rs770295734	snp	C/G	6.59e-05	0.00573983	missense	RFWD3	GRCh38.p7	16:74651950	CTCCAGATTCCTCTG[C/G]CTGGTCAACAACCCC	55159
rs770295813	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	RFWD3	GRCh38.p7	16:74636497	GCCCTGGCTGGAGGG[C/T]GAGCAGCTCAGGACC	55159
rs770348930	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74658162	ACCAACTTTGAATTT[G/T]GCTCCTTCCCTACTC	55159
rs770356663	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667357	TTGAATTTCGGAGCC[C/T]GTAAAGAGGCGTAGG	55159
rs770361364	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74661811	ATATGGACATTCACC[-/A]AAATCAAATGCATAT	55159
rs770450492	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74641817	TGTAATCCCGGCTAC[C/T]TGGGAGACTGAGGCA	55159
rs770451045	in-del	-/TTC			intron-variant	RFWD3	GRCh38.p7	16:74657476	ACCCAGGTTTTCTTT[-/TTC]TTTTTTTTTTTTTTT	55159
rs770502538	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74665321	GTCAGGCGCGGTGGC[C/T]CACACCTGTAATCCC	55159
rs770536983	in-del	-/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662103	TCTTTAATTCCATTG[-/T]TATCAGTTTGAAAAC	55159
rs770613608	snp	A/C	8.24436e-05	0.00641989	missense	RFWD3	GRCh38.p7	16:74652049	GATTCCTAGTCTCTG[A/C]ATCATAAGTGGTAGC	55159
rs770618997	snp	C/T	1.67008e-05	0.00288965	splice-acceptor-variant, intron-variant	RFWD3	GRCh38.p7	16:74630958	GTATTTGTCTCCAGG[C/T]TGTGGAGTTACAAAA	55159
rs770626727	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660181	CTAACTCCTCTATTC[C/T]ATAGTTATGAGACCC	55159
rs770650354	snp	C/T	1.74376e-05	0.00295271	intron-variant	RFWD3	GRCh38.p7	16:74632699	CAAAATAGTATGAAA[C/T]AGATCACTGAAAGTG	55159
rs770661821	snp	A/C/G	3.31638e-05	0.00407198	missense	RFWD3	GRCh38.p7	16:74661347	GAACAGGCTGGAGGA[A/C/G]GGCTGGTCCCCCTTG	55159
rs770712586	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74637519	GTAATCCCAGCACCT[C/T]GAGATGCTGAGGCTG	55159
rs770812326	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645436	CATTGAATGATCCCA[A/G]AGGTACTTAAATAAA	55159
rs770817600	snp	C/T	3.38078e-05	0.00411129	missense	RFWD3	GRCh38.p7	16:74637899	TTATCAGTGAGGACC[C/T]GCAGTTGGAGTCGGC	55159
rs770828966	in-del	-/AGA			intron-variant	RFWD3	GRCh38.p7	16:74666220	GATAGATAGATAGAT[-/AGA]TTGATTAGATACATA	55159
rs770870074	snp	G/T	0.000181185	0.00951628	synonymous-codon	RFWD3	GRCh38.p7	16:74626382	CCCAGTACACACCAG[G/T]ATGTTGCCATCATTC	55159
rs770870505	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74655743	TTAGCCAGGATGGTC[A/T]CACCCATCTCCTGAC	55159
rs770936794	snp	C/G	3.29734e-05	0.00406025	missense	RFWD3	GRCh38.p7	16:74628566	AGTCCATTTTCTGTT[C/G]CCAGAATGAAGCATC	55159
rs770985780	snp	C/T	1.6633e-05	0.00288378	synonymous-codon	RFWD3	GRCh38.p7	16:74660946	CCTGGCACTGTCTGT[C/T]CTCTGAGACCCTCCG	55159
rs771003934	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655954	CCTTTAAATATATTA[C/T]TGCTCATTGACAATG	55159
rs771022616	snp	C/T	1.64732e-05	0.0028699	missense	RFWD3	GRCh38.p7	16:74661130	ATGGTGTGATTACCA[C/T]CAGATCCCTGCCTAT	55159
rs771028907	in-del	-/AAA			intron-variant	RFWD3	GRCh38.p7	16:74646935	AACAACAACAACAAC[-/AAA]ATTAGCCAGGTGTGG	55159
rs771098978	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74653245	TTGGGAGGCCAAGGT[A/G]GGAGGATGGCTTGAG	55159
rs771117436	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662735	GGCCTTGGTAAGGAG[C/T]TTCTTCTATGTTAGG	55159
rs771117691	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74637787	GTTTCTGAGATGAAC[A/G]TAACTAACATTAGCT	55159
rs771207276	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74635377	GAGGCTGAGGCAGGA[C/G]AATCTCTTGAATCCA	55159
rs771219278	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74654600	AGTGTTCAAATTAAG[A/G]GAAGAGTCAGGCATC	55159
rs771223395	in-del	-/GT	1.6643e-05	0.00288465	frameshift-variant	RFWD3	GRCh38.p7	16:74626542	ACACTTCGTATGGTG[-/GT]GTGATTTTTATCTAT	55159
rs771261618	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659669	AGGCATCTGTCATCC[C/T]TGATGGGCACTACAG	55159
rs771324434	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623285	ACTGGGCCTGCCAAT[A/G]TCCCAGCACTTCACA	55159
rs771380114	snp	C/T	0.000115311	0.00759224	missense	RFWD3	GRCh38.p7	16:74636475	AGTGGTACTTGTGCT[C/T]GTGCTGGCCCTGGCT	55159
rs771405692	snp	A/C/G	6.59243e-05	0.00574094	intron-variant	RFWD3	GRCh38.p7	16:74649230	TTCCAGAAATGACAG[A/C/G]AGAGGTAAAATACAA	55159
rs771422126	snp	A/G	5.01098e-05	0.00500524	synonymous-codon	RFWD3	GRCh38.p7	16:74661399	AGCTGGCTGTTGTTC[A/G]GCATGATTTAACTGC	55159
rs771424665	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74631262	TCTGAGGCAGACAGA[C/T]CACTTGAGGTCAGGA	55159
rs771430026	snp	C/G	1.64898e-05	0.00287135	missense	RFWD3	GRCh38.p7	16:74649134	ATGTTCATATTACCT[C/G]TTTGGGGAGGGTCTT	55159
rs771455866	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74655942	GAAAAAAGGATTCCT[A/T]TAAATATATTACTGC	55159
rs771457614	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74665369	AGGGCAGACCACTTG[A/T]GGTCGGAGTCCCAGA	55159
rs771474037	snp	G/T	1.69112e-05	0.0029078	missense	RFWD3	GRCh38.p7	16:74637891	TAGTGCACTTATCAG[G/T]GAGGACCTGCAGTTG	55159
rs771593849	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643922	GACCTTGTGATCTGC[C/T]CACCTTGGCCTCCCA	55159
rs771662376	snp	A/G	6.60437e-05	0.00574608	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630822	CACATGACTGCTCGT[A/G]TTTCGCACGTCATAT	55159
rs771693864	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624652	TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTGGG	55159
rs771700177	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74655407	ACCACGCCTGGCTAA[-/T]TTTTTTTTTTTTTGT	55159
rs771738848	snp	C/T	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74626450	TGCAAGTAGGTCCTC[C/T]AAAAAATGTATGTAC	55159
rs771760258	snp	A/C/G	8.56556e-05	0.00654381	intron-variant	RFWD3	GRCh38.p7	16:74624112	GTCAGGAGTCAGTCA[A/C/G]TACACGAAGGGACTT	55159
rs771780584	snp	A/C	1.64741e-05	0.00286998	missense	RFWD3	GRCh38.p7	16:74644569	CGTACTTGTCCTTTA[A/C]GCCACGTGGAAATGC	55159
rs771783157	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74666108	GGGGAAGGGAGAGAG[C/G]GAAAGAAGGAAATTA	55159
rs771784627	in-del	CCCACAAAA/TGGGCAACAAGAGCAAAACTCCGTCTCC			intron-variant	RFWD3	GRCh38.p7	16:74641901	CATTGCAATCCAGCC[lengthTooLong]AAAAAAAAAAAAAAA	55159
rs771799855	snp	C/G	1.96342e-05	0.00313316	missense	RFWD3	GRCh38.p7	16:74637958	CCTTAGCATCTGTTC[C/G]TTCAGTAGGGAACTA	55159
rs771811036	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74646469	GTGTGCCACCATACA[C/G]CAACCATGCTTTACA	55159
rs771811419	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624968	CACTCCAGCCTGGAC[C/T]GAGTAAGATACTGTC	55159
rs771935954	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74631240	TGTAATCCCAGCACT[A/T]TGGGATTCTGAGGCA	55159
rs771949895	snp	A/G	0.000214145	0.0103454	missense	RFWD3	GRCh38.p7	16:74651971	CAACAACCCCTCCAT[A/G]CTCTGCAGAGCTGTC	55159
rs771989831	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74633328	ACCCATGCTTGCTTC[A/C]TGACAATGAAGAGAA	55159
rs772025978	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74666413	ATGAAGTAATCGGCG[A/C]TCAGAGCGGGCGCAG	55159
rs772053959	in-del	C/TTTTTTTTTTTTTT			intron-variant	RFWD3	GRCh38.p7	16:74643670	TGTTACTAGCAACTG[C/TTTTTTTTTTTTTT]TTTTTTTTTTGAGAC	55159
rs772065673	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74661870	ATTAATCTTTCACAG[A/C]ATCAACAGTTACAAG	55159
rs772079486	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652311	TATTATTTTTTACCA[C/T]TCAACCACTGCTACA	55159
rs772089430	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74632465	TAACACCGATACGAA[C/T]TCCATGCTACTCAAC	55159
rs772096137	snp	A/T	1.64732e-05	0.0028699	missense	RFWD3	GRCh38.p7	16:74626362	GCAGAATTTGCTGCT[A/T]CATCCCCAGTACACA	55159
rs772156515	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74636398	CACCAGGCAGCTCAG[A/G]GCATCACAGTATGCC	55159
rs772211314	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74659157	TTTATAAGTGTCACC[C/G]TTAAGTTGGTTAATA	55159
rs772286324	in-del	-/CAGTACTCAA	1.65296e-05	0.00287481	frameshift-variant	RFWD3	GRCh38.p7	16:74632647	TGCTCTTCATGTTGG[-/CAGTACTCAA]CATCTTAACACCAAA	55159
rs772332010	snp	C/T	1.64825e-05	0.00287071	synonymous-codon	RFWD3	GRCh38.p7	16:74628531	TGGCTCCAAGGGCAG[C/T]ACATGAGGCCAATGA	55159
rs772372251	snp	C/T	3.3418e-05	0.00408753	missense	RFWD3	GRCh38.p7	16:74660941	ATTTACCTGGCACTG[C/T]CTGTCCTCTGAGACC	55159
rs772403065	in-del	-/CTGTTTTTTTTTT			intron-variant	RFWD3	GRCh38.p7	16:74643667	TGGTGTTACTAGCAA[-/CTGTTTTTTTTTT]TTTTTTTTTTTTTTG	55159
rs772432821	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74642357	TCAAACTCCTGAGCT[C/G]AGGCGATCTGCCTGC	55159
rs772432980	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74654256	GTTGATCTTTTAGAA[C/G]AACCAACTTTTTGAT	55159
rs772450785	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623498	AAATCAGTACCAAGA[C/T]GATGGTTAGTCCCTT	55159
rs772460092	snp	A/C/T	3.33474e-05	0.00408323	synonymous-codon	RFWD3	GRCh38.p7	16:74644733	AGACTTCTGGGGAGA[A/C/T]GGCTAGATGGAAAGC	55159
rs772499588	snp	A/G	1.66366e-05	0.0028841	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623904	TCTAACCAGCAGCAT[A/G]CCTTCAAGGTTTCGA	55159
rs772544946	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74638319	AAACAGTAAGCTGTT[C/G]GTTGTTCATGAGATA	55159
rs772624729	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74633580	GTAGTGACAAAAAGC[A/G]GTGACTGCTGGGGAT	55159
rs772644101	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74659086	TTTTCTCACTAGAGT[G/T]TGGCTTCTGTTTGGC	55159
rs772683260	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant	RFWD3	GRCh38.p7	16:74630890	AGTTAGCCTCATCAA[A/G]ACACCAGCAACAGCT	55159
rs772747154	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74625974	GCAGATCACTTGAGG[C/T]CAGGAGTTCCAGACC	55159
rs772762155	snp	A/G	1.69043e-05	0.00290721	synonymous-codon	RFWD3	GRCh38.p7	16:74637892	AGTGCACTTATCAGT[A/G]AGGACCTGCAGTTGG	55159
rs772917763	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74627000	GGGAAACATGTATCT[C/G]AAATTCTGCTGGGAG	55159
rs772922451	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RFWD3	GRCh38.p7	16:74661171	AGTTCTTGGATTGAT[A/G]TTCTCCACAGTGTCT	55159
rs772951020	snp	C/T	4.95152e-05	0.00497545	missense, intron-variant	RFWD3	GRCh38.p7	16:74630826	TGACTGCTCGTGTTT[C/T]GCACGTCATATACCA	55159
rs772961110	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74636137	ATCATGGTTATCAGT[A/G]TTTCTACCCTCTTGG	55159
rs772992025	in-del	-/AG	1.64768e-05	0.00287021	frameshift-variant	RFWD3	GRCh38.p7	16:74632555	GTTGTCTAGGGAAGC[-/AG]AGAGTAGCAAGCCTC	55159
rs773019021	in-del	-/AGAC			intron-variant	RFWD3	GRCh38.p7	16:74666175	ATAGATAGATTAGAT[-/AGAC]AGATTAGATAGATAG	55159
rs773023748	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74666400	CAACTTTAAAGTGAT[A/G]AAGTAATCGGCGCTC	55159
rs773031230	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664396	GGGGAGAAATGGACT[A/G]AAAAGAGCAGAATCT	55159
rs773039703	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74647732	GAGTAGCTGGGATTA[C/T]ATGCGCCTGCCAACA	55159
rs773057276	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643777	GCCTCACGGGTTCAC[A/G]CCATTCTCCTGTCTC	55159
rs773131455	snp	G/T	3.29652e-05	0.00405974	missense	RFWD3	GRCh38.p7	16:74652037	CTTCAGATACAGGAT[G/T]CCTAGTCTCTGAATC	55159
rs773181922	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668446	ACAATCAAAGGAGCT[G/T]CAGGCCGGCCATTAG	55159
rs773249458	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74654576	TTAGTAACTCTACAA[C/T]GGCCTCTAAGTGTTC	55159
rs773252083	in-del	-/CT			intron-variant	RFWD3	GRCh38.p7	16:74655197	CAAAGGACAGGCTGA[-/CT]CTCTTGTTAGGGGAT	55159
rs773296420	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74631383	AGGCTGAGGCAGGAG[-/A]ATCACTTGAACCCTG	55159
rs773329209	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74624874	GTGCATGCCCGCAGT[C/G]CCAGCTACTCAAGAG	55159
rs773340289	snp	A/G	2.05878e-05	0.00320834	intron-variant	RFWD3	GRCh38.p7	16:74626604	GACGCTACACAAAAA[A/G]TTAACCAAGTACCCA	55159
rs773350818	in-del	-/AGA			intron-variant	RFWD3	GRCh38.p7	16:74666208	GATAGATAGATAGAT[-/AGA]TAGATAGATAGATTG	55159
rs773387617	snp	C/T	1.80413e-05	0.00300338	intron-variant	RFWD3	GRCh38.p7	16:74652169	TACAATGAACTATCA[C/T]CACAAAAACAATCTA	55159
rs773425069	snp	A/G			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621383	TGAAAGAGACAAAAG[A/G]CACTAGGAGCCATTA	55159
rs773500795	in-del	-/C	1.64787e-05	0.00287038	frameshift-variant	RFWD3	GRCh38.p7	16:74649150	TTGGGGAGGGTCTTG[-/C]CCTCCATCGATACAT	55159
rs773502401	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624462	GTGCAGTGGCACGAT[C/T]TTGGCTTACTGCAAC	55159
rs773516896	snp	C/T	1.66355e-05	0.002884	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623905	CTAACCAGCAGCATG[C/T]CTTCAAGGTTTCGAG	55159
rs773544480	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74631138	TTTAAATTCCATAAC[A/G]TTTGTTTTGGGGGCC	55159
rs773583961	snp	C/T	1.66918e-05	0.00288888	missense	RFWD3	GRCh38.p7	16:74660942	TTTACCTGGCACTGT[C/T]TGTCCTCTGAGACCC	55159
rs773644975	snp	A/C	1.64795e-05	0.00287045	synonymous-codon	RFWD3	GRCh38.p7	16:74626502	ATTTCCAGTGTCATC[A/C]AGTCGGTAGGACATT	55159
rs773680864	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623290	GCCTGCCAATGTCCC[A/G]GCACTTCACACCTGG	55159
rs773695232	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622384	AATTTTGGCACTTTA[A/G]GAGGCTGAGGTGGGA	55159
rs773701779	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74636405	CAGCTCAGAGCATCA[C/T]AGTATGCCATGATCC	55159
rs773740906	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630396	AGCCACCGCACCCAG[C/T]GACATGTGGCTATTA	55159
rs773795460	snp	C/T	1.64961e-05	0.00287189	splice-donor-variant	RFWD3	GRCh38.p7	16:74649131	ATGATGTTCATATTA[C/T]CTGTTTGGGGAGGGT	55159
rs773952889	snp	A/C	1.64743e-05	0.00287	missense	RFWD3	GRCh38.p7	16:74651967	TGGTCAACAACCCCT[A/C]CATACTCTGCAGAGC	55159
rs773976659	snp	C/T			splice-acceptor-variant	RFWD3	GRCh38.p7	16:74628668	AGACCAGTGGGCATC[C/T]GAAAGGAAAGTAAGG	55159
rs774041421	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74641850	AGAATTGCTTGAACC[C/T]GGGAGGCGGGAAGTT	55159
rs774078573	snp	C/T	3.6806e-05	0.00428971	intron-variant	RFWD3	GRCh38.p7	16:74636618	ACAAAGCTTTTTAAT[C/T]TGATATTCCCCTCAA	55159
rs774084387	snp	A/G	6.7202e-05	0.00579625	intron-variant	RFWD3	GRCh38.p7	16:74628710	CACACTCCAAAACTC[A/G]GACGGCTCCAGACCC	55159
rs774107769	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643832	AGGCGTCCGCCACTA[C/T]GCCCGGCTAATTTTT	55159
rs774144805	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74666275	ACTACATGGGGAAAC[-/TT]TGGGCGGGTTTCCTA	55159
rs774150579	snp	A/G	1.66346e-05	0.00288393	intron-variant	RFWD3	GRCh38.p7	16:74651882	TTAAGCTTCATGGAT[A/G]TTAGCCTTGTGAGTC	55159
rs774150583	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74650521	TTCAGGTGGTATCAC[C/G]CTGGTCCCTGTATTA	55159
rs774178387	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74627614	CAGGGCTCTTCTAGA[C/G]AGTCACTATCTCAAG	55159
rs774180264	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74638237	AGCTAATCTAGTGTT[C/G]AGCTACGGCAAATTG	55159
rs774204237	in-del	-/GAGATCACACCCCTCCCTGCATTCCAGCCCGG			intron-variant	RFWD3	GRCh38.p7	16:74633899	AGGTTGTAATGAGCT[lengthTooLong]GAGATCACACCCCTC	55159
rs774255816	snp	A/C	1.75004e-05	0.00295802	intron-variant	RFWD3	GRCh38.p7	16:74631006	TAAGAAAATCAAATA[A/C]ATGACAAAGATGTAA	55159
rs774281771	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630634	TTAATAAGAATGTTA[C/T]TGATTCTGAAGTGAG	55159
rs774316866	snp	C/G			missense	RFWD3	GRCh38.p7	16:74644570	GTACTTGTCCTTTAA[C/G]CCACGTGGAAATGCA	55159
rs774369310	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74625932	GGCTCACGCCTCTAA[G/T]CCCAGCACTTTGGGA	55159
rs774380663	snp	A/T	1.69925e-05	0.00291478	missense	RFWD3	GRCh38.p7	16:74624043	GTCTGTAGGTCCTGG[A/T]GCAACGAGCCACTGG	55159
rs774419356	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74664990	ACCCCAAACCTTGAG[G/T]ATGTCACACAAACGC	55159
rs774430995	in-del	-/C	6.67267e-05	0.00577572	intron-variant	RFWD3	GRCh38.p7	16:74628426	GTGCTCCCAAATAAG[-/C]TATGGGAGACCCCAG	55159
rs774465649	snp	C/T	1.78036e-05	0.00298353	intron-variant	RFWD3	GRCh38.p7	16:74632713	ATAGATCACTGAAAG[C/T]GAACCTAGGGCAATT	55159
rs774480180	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74641323	GCGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT	55159
rs774519634	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74635700	CTTAGATGGGATAAA[-/G]GAACATTATATAACC	55159
rs774578244	snp	A/G	1.85948e-05	0.00304911	intron-variant	RFWD3	GRCh38.p7	16:74626584	AATCAGTGCTGCACC[A/G]TGGGGACGCTACACA	55159
rs774617901	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661168	TGAAGTTCTTGGATT[A/G]ATGTTCTCCACAGTG	55159
rs774649273	snp	C/T			missense	RFWD3	GRCh38.p7	16:74626530	ATTTCCATCAGCACA[C/T]TTCGTATGGTGGTGT	55159
rs774674240	snp	C/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623428	CCGGACACAAGGTTC[C/T]ACAGTGCCCTCTTGT	55159
rs774708392	snp	C/T	1.74152e-05	0.00295082	intron-variant	RFWD3	GRCh38.p7	16:74652154	ACAACGGAATTATAG[C/T]ACAATGAACTATCAT	55159
rs774724655	snp	A/G	1.65146e-05	0.0028735	synonymous-codon	RFWD3	GRCh38.p7	16:74652080	TGGCAAGTCAGGCTG[A/G]GTCCTGCTCACCTGA	55159
rs774759415	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653372	TGACACCCAAAAAAC[C/T]TGGGAGGCTGAGGCA	55159
rs774770054	snp	C/T	3.2994e-05	0.00406152	missense	RFWD3	GRCh38.p7	16:74632634	GGAATGTACTGACTG[C/T]TCTTCATGTTGGCAG	55159
rs774805259	in-del	-/AC			intron-variant	RFWD3	GRCh38.p7	16:74653034	AGGAAGGATCTAGGG[-/AC]ACACACACACACAGA	55159
rs774808048	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74666187	GATAGACAGATTAGA[C/T]AGATAGATAGATAGA	55159
rs774837280	snp	C/G	1.66161e-05	0.00288232	synonymous-codon	RFWD3	GRCh38.p7	16:74644727	AGGCTCAGACTTCTG[C/G]GGAGATGGCTAGATG	55159
rs774862468	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74631567	TTATAAAGGCACGGA[A/G]CACACTCACATCTGG	55159
rs774863029	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74656875	TGGATGACTTTTGCC[A/G]GGCTCAAGACTTCAG	55159
rs774884855	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658240	TGTGTTATTCACCAA[C/T]ATATCTAGGGCAAAG	55159
rs774944352	snp	A/G	1.64754e-05	0.00287009	missense	RFWD3	GRCh38.p7	16:74661247	GCAGGCTGGAGCAGG[A/G]GTGGTGTCGCTTGGC	55159
rs774953889	snp	C/G	1.89708e-05	0.00307978	intron-variant	RFWD3	GRCh38.p7	16:74624091	AGAACACAAGCAGAG[C/G]GAAGGGTCAGGAGTC	55159
rs774978765	snp	C/G	1.64991e-05	0.00287215	missense	RFWD3	GRCh38.p7	16:74644657	TGGTCCACTGTTCCA[C/G]ACATATTGTACAAGT	55159
rs775003580	in-del	-/AAC	3.3379e-05	0.00408514	cds-indel	RFWD3	GRCh38.p7	16:74623882	TGCTAGGCGCTAGCA[-/AAC]AACATCTAACCAGCA	55159
rs775043994	snp	C/T	1.66571e-05	0.00288587	missense	RFWD3	GRCh38.p7	16:74624026	CCAACACAGGCTGAT[C/T]GGTCTGTAGGTCCTG	55159
rs775059394	in-del	-/TTT			intron-variant	RFWD3	GRCh38.p7	16:74639038	CATTGAGCTAAGACT[-/TTT]TTTTTTTTTTTTTTT	55159
rs775101752	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74665371	GGCAGACCACTTGAG[G/T]TCGGAGTCCCAGAAT	55159
rs775102603	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74626261	GCTATATGAGCTTCT[A/G]TAAAAAAAGTTCATG	55159
rs775103807	snp	A/G	5.01467e-05	0.00500708	missense	RFWD3	GRCh38.p7	16:74661404	GCTGTTGTTCGGCAT[A/G]ATTTAACTGCACCTG	55159
rs775146609	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639360	CCATTTCAATGATTA[C/T]AACATCACTTACGCA	55159
rs775176306	snp	C/T	1.6477e-05	0.00287024	missense	RFWD3	GRCh38.p7	16:74649158	GGGTCTTGCCTCCAT[C/T]GATACATGTAACTTC	55159
rs775211294	snp	C/G	1.6476e-05	0.00287014	missense	RFWD3	GRCh38.p7	16:74636512	TGAGCAGCTCAGGAC[C/G]CATGCTTGGGAGCCC	55159
rs775265788	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74655996	CCAAGAGCTCTGAAG[A/G]TGATTAATGTTATTT	55159
rs775319334	snp	A/C	1.64732e-05	0.0028699	intron-variant	RFWD3	GRCh38.p7	16:74644340	AGGGAACATTCCAGC[A/C]AGGCATACTCTTACC	55159
rs775345045	snp	C/T	1.64953e-05	0.00287182	missense	RFWD3	GRCh38.p7	16:74623941	AGTCACTCCCACTTA[C/T]AGATGTGGACCATCT	55159
rs775355407	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634395	ATATATATATATATA[C/T]ATATTTTGAGACAAG	55159
rs775402876	snp	A/G	2.27446e-05	0.00337221	intron-variant	RFWD3	GRCh38.p7	16:74637979	TAGGGAACTAGAGGG[A/G]GAAAGCCAGCAACAA	55159
rs775417423	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622865	TGGGGAAGGCTTTAA[C/G]TGGATAACTGGAATG	55159
rs775444971	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74635213	ACCCGAGAGGTGGAG[A/C]TTGCAGTGAGCCGAG	55159
rs775475067	snp	C/G	1.69123e-05	0.0029079	synonymous-codon	RFWD3	GRCh38.p7	16:74660934	TATATTTATTTACCT[C/G]GCACTGTCTGTCCTC	55159
rs775555707	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659178	TTGGTTAATACAAGT[C/T]ACTGTGCTTGACCAA	55159
rs775594158	in-del	-/A	1.6949e-05	0.00291105	intron-variant	RFWD3	GRCh38.p7	16:74632677	TAACACCAAAGCCTG[-/A]AAAAGGCAAAATAGT	55159
rs775613829	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74631636	GTGACTAAGGGTATA[A/G]AAGAAGTCATCATGG	55159
rs775662420	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74666466	GGCTAGGCTCTCGGG[A/G]GAAGGGCCGGGCGAC	55159
rs775682125	in-del	-/AATAAATAAATAGATT	2.67641e-05	0.00365805	intron-variant	RFWD3	GRCh38.p7	16:74649092	CTCTAAAAATAAATA[-/AATAAATAAATAGATT]TTTTTAAAATGATGT	55159
rs775719646	snp	C/T	3.51673e-05	0.00419314	intron-variant	RFWD3	GRCh38.p7	16:74632706	GTATGAAATAGATCA[C/T]TGAAAGTGAACCTAG	55159
rs775745004	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74666626	CGACCACTGGCGCCG[-/C]CCCCGAGGGCCCGAA	55159
rs775775978	in-del	-/AAAT	0.000534045	0.0163321	intron-variant	RFWD3	GRCh38.p7	16:74649083	AGACCTAGTCTCTAA[-/AAAT]AAATAAATAAATAAA	55159
rs775796008	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	RFWD3	GRCh38.p7	16:74626385	AGTACACACCAGGAT[A/G]TTGCCATCATTCTCT	55159
rs775879641	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74624283	ATCAGCAATTAGTCT[A/G]CCTGTAAGTGGACCT	55159
rs775933474	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74659725	CCCCAACATTAAAAT[C/G]AGCAGGATCCATGAA	55159
rs775958516	in-del	-/TTATT			intron-variant	RFWD3	GRCh38.p7	16:74647287	AATGATGTATAGGTG[-/TTATT]TTTATTTTTTTTTTG	55159
rs775961760	snp	A/G	1.66568e-05	0.00288585	intron-variant	RFWD3	GRCh38.p7	16:74628698	GAAACTGTATCTCAC[A/G]CTCCAAAACTCGGAC	55159
rs775970172	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	RFWD3	GRCh38.p7	16:74661153	CTGCCTATGTTGTTC[C/T]GAAGTTCTTGGATTG	55159
rs775986566	snp	C/T	0.000197655	0.00993922	missense	RFWD3	GRCh38.p7	16:74661053	TCAGGAATTCCAGCA[C/T]GCCATGAAGTCTCTG	55159
rs775998162	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646701	TGAGGCAGGGGAATC[A/G]CTTGAACTCAGGAGG	55159
rs776022046	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648234	TTAAATCTAAGAGAC[A/G]GCAGTCACACAAATA	55159
rs776051785	snp	G/T	2.2269e-05	0.00333676	intron-variant	RFWD3	GRCh38.p7	16:74636591	TCCTAAAATGAAAAA[G/T]ATTTTATAAATACAA	55159
rs776051837	snp	C/T	4.94858e-05	0.00497398	synonymous-codon	RFWD3	GRCh38.p7	16:74628582	CCAGAATGAAGCATC[C/T]TCCAAGGTTCCAGCC	55159
rs776176666	snp	C/G	1.64741e-05	0.00286998	missense, intron-variant	RFWD3	GRCh38.p7	16:74630906	ACACCAGCAACAGCT[C/G]CAGACAGGACGTCCA	55159
rs776197652	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74635281	GAGCGAGACTCCATC[G/T]CAAAAAAATAAAAAA	55159
rs776244471	snp	C/T	4.94515e-05	0.00497225	synonymous-codon	RFWD3	GRCh38.p7	16:74661270	CGCTTGGCTGCTGAT[C/T]ACCTCAGCAGGAGCT	55159
rs776325529	snp	A/G			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662064	AAATATTTATTAAGC[A/G]CCTATGTTCTTTTCA	55159
rs776382100	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657056	CCAGGGAAAATGATT[C/T]AGGCTTTTCACACTC	55159
rs776394816	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74645950	AGACGGGGTTTCACC[G/T]TGTTAGTTAGGATGG	55159
rs776440143	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74646187	TGAAACCAGACTGGA[C/T]AACATAGCAAGACCT	55159
rs776453305	snp	A/G	0.000154832	0.00879727	intron-variant	RFWD3	GRCh38.p7	16:74652144	ACACAGAAAGACAAC[A/G]GAATTATAGTACAAT	55159
rs776480532	snp	C/G	2.20291e-05	0.00331874	intron-variant	RFWD3	GRCh38.p7	16:74637974	TTCAGTAGGGAACTA[C/G]AGGGGGAAAGCCAGC	55159
rs776507784	in-del	-/AGA			intron-variant	RFWD3	GRCh38.p7	16:74666212	GATAGATAGATAGAT[-/AGA]TAGATAGATTGATTA	55159
rs776526678	snp	A/G	0.000280318	0.0118355	synonymous-codon	RFWD3	GRCh38.p7	16:74652053	CCTAGTCTCTGAATC[A/G]TAAGTGGTAGCTGGC	55159
rs776553550	snp	C/T	1.64743e-05	0.00287	missense	RFWD3	GRCh38.p7	16:74626465	CAAAAAATGTATGTA[C/T]AGGCTGGCAGGAGCA	55159
rs776568931	snp	C/T	1.69246e-05	0.00290896	synonymous-codon	RFWD3	GRCh38.p7	16:74637904	AGTGAGGACCTGCAG[C/T]TGGAGTCGGCACTGT	55159
rs776577009	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74626031	TCTCTACTAAAAATA[C/T]AAAAATCAGTCGGGC	55159
rs776588557	in-del	-/AGACCAGCCTGGGAAACATGGCAAAACCCTGTCTCTACTAAAAATACACA	1.6473e-05	0.00286988	frameshift-variant	RFWD3	GRCh38.p7	16:74626427	ATGGCATTTTTGGTC[lengthTooLong]AATAGTTTGCAAGTA	55159
rs776607901	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668850	CATTGGAAAGCAAAC[A/C]AAAGATATATGAATG	55159
rs776618448	snp	A/G	1.64732e-05	0.0028699	missense	RFWD3	GRCh38.p7	16:74661008	TTCTTGTTCTCATTG[A/G]CCCTACACTGTGGTT	55159
rs776630008	in-del	-/A	9.98821e-05	0.00706619	intron-variant	RFWD3	GRCh38.p7	16:74649105	TAAATAAATAAATAG[-/A]TTTTTTTAAAATGAT	55159
rs776661298	snp	A/G			missense	RFWD3	GRCh38.p7	16:74644404	TCCAAAGCTCTCAGG[A/G]TTCGGGCATAAAGGA	55159
rs776695648	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74649602	AGAATTCTTTTTTTA[A/T]ATAAACACTGTGTAA	55159
rs776708781	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74633920	ACACCCCTCCCTGCA[-/T]TCCAGCCCGGGAGAT	55159
rs776744870	snp	A/G	3.29473e-05	0.00405864	intron-variant	RFWD3	GRCh38.p7	16:74644469	CTAAAGAACCCAATA[A/G]GACATAATTAGAGTG	55159
rs776763776	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74652679	ATCAAACAAAATAAC[C/T]TAGAATGATGAGAAG	55159
rs776773920	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659856	GGGTAATAGATGACC[C/T]AGCTACCACTTTTTA	55159
rs776833419	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74624371	GTCAATAAGATAAAG[C/T]CCCTGTCTTTGCCCT	55159
rs776841919	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629419	ATCCCAGCACTTCGG[A/G]AAGCCGAGGTGGGAG	55159
rs776928078	snp	A/T	1.65012e-05	0.00287234	intron-variant	RFWD3	GRCh38.p7	16:74632519	ACTTCCCCAAATCAC[A/T]CACCTGGTCAGTTTA	55159
rs776938376	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74632721	CTGAAAGTGAACCTA[G/T]GGCAATTCAAACTAG	55159
rs776941268	snp	G/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621632	GCCCAGAAGACTAAA[G/T]CCTGGATTTATAAAT	55159
rs777027970	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74633921	CACCCCTCCCTGCAT[G/T]CCAGCCCGGGAGATC	55159
rs777034036	snp	C/T	0.000233244	0.0107966	intron-variant	RFWD3	GRCh38.p7	16:74628429	CTCCCAAATAAGCTA[C/T]GGGAGACCCCAGCAC	55159
rs777121038	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638176	GGAATTTGACTATTA[C/T]TAGAAAATGGGGACT	55159
rs777137273	snp	C/T	1.64923e-05	0.00287156	synonymous-codon	RFWD3	GRCh38.p7	16:74628573	TTTCTGTTCCCAGAA[C/T]GAAGCATCCTCCAAG	55159
rs777160067	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74639455	CCAAAGGTCATTATG[A/C]AGCACGTGACTGTAA	55159
rs777180107	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658970	GATGGGGTTTCACCA[C/T]GTTGGCCTCGAACTC	55159
rs777184221	snp	C/T	1.65913e-05	0.00288017	synonymous-codon	RFWD3	GRCh38.p7	16:74660949	GGCACTGTCTGTCCT[C/T]TGAGACCCTCCGGCT	55159
rs777224972	snp	C/T	9.88386e-05	0.00702919	missense	RFWD3	GRCh38.p7	16:74636484	TGTGCTTGTGCTGGC[C/T]CTGGCTGGAGGGTGA	55159
rs777317420	snp	A/C	8.3266e-05	0.00645183	missense	RFWD3	GRCh38.p7	16:74652119	ATCCAATGGTGCTCT[A/C]AACCTATGTACACAG	55159
rs777400019	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74629196	CAGAAATATCATCCT[A/T]CCGACTGTGTTCCTA	55159
rs777416233	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623206	CTTTCCTTACCTTTC[A/G]CAAAGCAATGAACTT	55159
rs777426738	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655702	CTAATTTGTTGTATT[C/T]TTAGTGGAGACGGGG	55159
rs777430520	snp	A/C	1.7699e-05	0.00297475	intron-variant	RFWD3	GRCh38.p7	16:74660899	AATTTCTAGTACAGC[A/C]ATGATCACAGACTTA	55159
rs777436206	snp	A/G	2.02468e-05	0.00318167	synonymous-codon	RFWD3	GRCh38.p7	16:74637963	GCATCTGTTCCTTCA[A/G]TAGGGAACTAGAGGG	55159
rs777450273	in-del	-/GAA	0.000106651	0.00730167	intron-variant	RFWD3	GRCh38.p7	16:74644788	TGTAAAATCAATCTT[-/GAA]GAAGATGTGCAACTA	55159
rs777484856	snp	C/T	1.65386e-05	0.00287559	missense	RFWD3	GRCh38.p7	16:74644687	TGTCCCCTTCTTCCT[C/T]ATCCATAGAAGCAGA	55159
rs777492633	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74650102	TTTATGTAAGTGGAA[A/T]CATAAACTATGTTGG	55159
rs777494682	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74665252	TGGTGTTCCAGACCA[C/G]CTTGGGCAACACAGT	55159
rs777520660	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74658956	GTATTTTTAGTAGAG[A/C]TGGGGTTTCACCATG	55159
rs777610851	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659573	GCACTCCAGCCTGAG[C/T]GACAGAGCAAGACTC	55159
rs777691381	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636917	GGGGTTTTACCACGT[C/T]GGCCGGGCTGGTCTT	55159
rs777732895	in-del	-/T	1.64735e-05	0.00286993	frameshift-variant	RFWD3	GRCh38.p7	16:74661204	TCCCAAGACCTCCAC[-/T]TCTGTCAGGTCAACA	55159
rs777776105	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622347	CTTCAAATAGGGGCC[C/G]GGTGCAGTGGCTCAC	55159
rs777778054	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641045	CAATATTTAGGTAAA[A/G]CTGAAATTAAATGTG	55159
rs777781500	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74626629	TACCCAAACCTCACA[C/T]GCTTACAACCTAGTT	55159
rs777790669	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74650318	ACAAACTATGCAAAC[C/T]GGTTGTTAGAAAACA	55159
rs777799464	snp	A/G	9.88924e-05	0.0070311	synonymous-codon	RFWD3	GRCh38.p7	16:74628543	CAGCACATGAGGCCA[A/G]TGAGAAAAGTCCATT	55159
rs777802762	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	RFWD3	GRCh38.p7	16:74626454	AGTAGGTCCTCCAAA[A/G]AATGTATGTACAGGC	55159
rs777804678	snp	A/C	6.61091e-05	0.00574893	intron-variant	RFWD3	GRCh38.p7	16:74636333	ATGAAAGCTGAGGTT[A/C]TAGACTCTTTACCTG	55159
rs777876447	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74638831	GTTCTGAGAAACATG[C/T]TGTTAGGTGATTTCG	55159
rs777955720	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74624290	ATTAGTCTACCTGTA[A/G]GTGGACCTGAAATAA	55159
rs777964337	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74655722	TGGAGACGGGGTTTC[A/T]CCGTGTTAGCCAGGA	55159
rs778044131	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643877	AGAGACGGGGTTTCA[C/T]CGTGTTAGCCAGGAT	55159
rs778085578	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74635878	AACACAAAACATGTT[G/T]AGAGAAAATTAACCT	55159
rs778101171	snp	A/C	1.76241e-05	0.00296846	synonymous-codon	RFWD3	GRCh38.p7	16:74624069	ACTGGCAGCATCCCA[A/C]AGCTAAAGAACACAA	55159
rs778143194	snp	A/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662570	GGGAAGTACTCTTTT[A/C]AAGAGTGAAAATTGG	55159
rs778157049	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645696	CATACATGTGGTCTG[C/T]CATAGACTGAACTAT	55159
rs778178523	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632109	AACAGAGCTAAGGTC[A/G]GCTGGGCGCAGTGGC	55159
rs778265025	snp	A/C/G	6.58917e-05	0.00573952	missense	RFWD3	GRCh38.p7	16:74626443	AATAGTTTGCAAGTA[A/C/G]GTCCTCCAAAAAATG	55159
rs778265382	snp	A/G	1.66679e-05	0.00288681	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630956	CGGTATTTGTCTCCA[A/G]GCTGTGGAGTTACAA	55159
rs778325122	snp	C/G	1.65652e-05	0.0028779	missense	RFWD3	GRCh38.p7	16:74661337	ACATCAGCAGGAACA[C/G]GCTGGAGGAGGGCTG	55159
rs778335558	snp	G/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663650	CCTGAGACATTTTTT[G/T]AAGAAAGGATAAATT	55159
rs778336988	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668265	TTCCTATTCTGCCAG[C/T]CACTGAATTCTCAGA	55159
rs778363097	snp	A/G	1.69533e-05	0.00291142	synonymous-codon	RFWD3	GRCh38.p7	16:74637886	AAGCCTAGTGCACTT[A/G]TCAGTGAGGACCTGC	55159
rs778454801	snp	C/G	1.64811e-05	0.00287059	missense	RFWD3	GRCh38.p7	16:74652031	GCAACTCTTCAGATA[C/G]AGGATTCCTAGTCTC	55159
rs778467224	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74650559	TCCCATCAACCCTGC[A/T]ACCTAATGGTTTTAG	55159
rs778542820	snp	C/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621036	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAAGCA	55159
rs778543307	in-del	-/AAC			intron-variant	RFWD3	GRCh38.p7	16:74632412	AACAAAACAAAACAA[-/AAC]AACAACAACAACAAA	55159
rs778553579	snp	C/G/T	3.29458e-05	0.00405857	missense	RFWD3	GRCh38.p7	16:74626354	TCACCAGGGCAGAAT[C/G/T]TGCTGCTTCATCCCC	55159
rs778563910	snp	A/G	1.65932e-05	0.00288034	missense	RFWD3	GRCh38.p7	16:74652112	AGTAAGCATCCAATG[A/G]TGCTCTCAACCTATG	55159
rs778617759	in-del	-/GCTGGCCATGCCAGCAGGA	1.66718e-05	0.00288715	frameshift-variant	RFWD3	GRCh38.p7	16:74661366	TGGTCCCCCTTGGCT[-/GCTGGCCATGCCAGCAGGA]GCTGGCTGTTGTTCG	55159
rs778635619	snp	A/G	0.00032424	0.0127285	intron-variant	RFWD3	GRCh38.p7	16:74632681	ACCAAAGCCTGAAAA[A/G]GGCAAAATAGTATGA	55159
rs778670817	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657886	AAGAAAAGCATTTCA[C/T]AAGAAGATTTAATCA	55159
rs778680421	in-del	-/C	1.64969e-05	0.00287196	frameshift-variant, intron-variant	RFWD3	GRCh38.p7	16:74630830	TGCTCGTGTTTCGCA[-/C]GTCATATACCAGAAT	55159
rs778681493	snp	A/G	1.73066e-05	0.0029416	intron-variant	RFWD3	GRCh38.p7	16:74630769	CCAGGAAAAGAGTGA[A/G]TGGCTCCCTACCTGG	55159
rs778816763	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639622	CCCTATAATAATTTT[C/T]AATGCAATTTCAATC	55159
rs778823044	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74627842	TTATAGCCACTCTCC[C/T]GACAGAGACCTCAAG	55159
rs778926157	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640527	TAAGTCAGGTGTGGT[A/G]GCATGCGCCTGTACT	55159
rs778938061	snp	A/G	1.64825e-05	0.00287071	synonymous-codon	RFWD3	GRCh38.p7	16:74632612	ACGGATCTGTTTGCC[A/G]TGCATCGGAATGTAC	55159
rs778938448	snp	C/T	1.6537e-05	0.00287545	synonymous-codon	RFWD3	GRCh38.p7	16:74644685	AGTGTCCCCTTCTTC[C/T]TCATCCATAGAAGCA	55159
rs779016269	snp	A/C	1.67239e-05	0.00289166	intron-variant	RFWD3	GRCh38.p7	16:74649116	ATAGATTTTTTTAAA[A/C]TGATGTTCATATTAC	55159
rs779030049	snp	C/T	3.29478e-05	0.00405867	missense	RFWD3	GRCh38.p7	16:74644560	GGACATTTTCGTACT[C/T]GTCCTTTAAGCCACG	55159
rs779036300	in-del	-/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663990	AGAACAAAGCCCTTC[-/T]TCCCCCTATGCACGA	55159
rs779050347	in-del	-/CA			intron-variant	RFWD3	GRCh38.p7	16:74630480	AAATACAACTAAGGT[-/CA]CACAACTTCTAAGTA	55159
rs779053297	snp	C/T	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74636456	ACTGTGAAGGTCTTT[C/T]GGAAGTGGTACTTGT	55159
rs779119344	snp	A/G	2.98458e-05	0.0038629	intron-variant	RFWD3	GRCh38.p7	16:74638010	GTGGGGATTAGGAAG[A/G]CTACAGAAGACTTCC	55159
rs779126903	snp	C/T			missense	RFWD3	GRCh38.p7	16:74637885	GAAGCCTAGTGCACT[C/T]ATCAGTGAGGACCTG	55159
rs779137738	snp	C/T	1.64757e-05	0.00287012	synonymous-codon	RFWD3	GRCh38.p7	16:74649195	TGCTGAGACACCTGC[C/T]AGTTGCTCTGCCAAG	55159
rs779179246	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662744	AAGGAGTTTCTTCTA[A/T]GTTAGGAATGCACTG	55159
rs779201465	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74625609	TGGAAGCCAGATCAG[C/G]TGTCTTATAGAACGC	55159
rs779285037	snp	A/C	1.65348e-05	0.00287526	synonymous-codon	RFWD3	GRCh38.p7	16:74661321	CCCCTGGCTGCTGAC[A/C]ACATCAGCAGGAACA	55159
rs779319807	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74632437	ACAACAAAAAACAGA[A/G]CTAAGGTCATCATAA	55159
rs779390145	snp	C/T	3.29468e-05	0.00405861	missense, intron-variant	RFWD3	GRCh38.p7	16:74630874	AGTCCAGCATAGATG[C/T]AGTTAGCCTCATCAA	55159
rs779404005	snp	C/G	3.29568e-05	0.00405923	missense	RFWD3	GRCh38.p7	16:74632595	CTGCTAAACGCCAGT[C/G]CACGGATCTGTTTGC	55159
rs779488270	snp	C/T	1.64743e-05	0.00287	missense	RFWD3	GRCh38.p7	16:74644554	ACCTGGGGACATTTT[C/T]GTACTTGTCCTTTAA	55159
rs779501435	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74655242	ACTTCAGTTGAAGCC[A/G]ATGCTCTTTTTTTTT	55159
rs779501903	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74644155	TGTTTAATGCTCTAC[A/C]TAAGGCAAACGATGC	55159
rs779504338	snp	G/T	1.64741e-05	0.00286998	missense	RFWD3	GRCh38.p7	16:74651954	AGATTCCTCTGCCTG[G/T]TCAACAACCCCTCCA	55159
rs779515611	snp	A/G	0.000166359	0.00911876	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623902	CATCTAACCAGCAGC[A/G]TGCCTTCAAGGTTTC	55159
rs779596485	snp	A/T	3.70233e-05	0.00430236	intron-variant	RFWD3	GRCh38.p7	16:74661481	TTTGTAAAAAGTATT[A/T]ATAAAATAGATAAAA	55159
rs779635998	snp	A/C	1.65094e-05	0.00287305	intron-variant	RFWD3	GRCh38.p7	16:74626320	CTACTTTTTATATGA[A/C]AGTAAAAAAGTAACA	55159
rs779676190	snp	C/T	1.65583e-05	0.00287731	intron-variant	RFWD3	GRCh38.p7	16:74632492	CAACACCAAAGAGCC[C/T]AGTCTCCACCTACTT	55159
rs779684950	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74637358	TAAGGCCAGGTGCAG[C/T]GCTCACGCCTGTAAT	55159
rs779686080	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74630191	ACCTCCGCCTCCGAG[G/T]CTCAATAGATTCTTC	55159
rs779745168	in-del	-/TAC	1.69269e-05	0.00290915	intron-variant	RFWD3	GRCh38.p7	16:74630980	GTTACAAAAGACTTT[-/TAC]AACTGCATTAAGAAA	55159
rs779763918	in-del	-/TTTT			intron-variant	RFWD3	GRCh38.p7	16:74639037	GCATTGAGCTAAGAC[-/TTTT]TTTTTTTTTTTTTTT	55159
rs779764440	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668060	AAAGGCGGACCTCTG[A/C]AGGCATTATTAACTA	55159
rs779783050	snp	A/C	4.94466e-05	0.00497201	missense	RFWD3	GRCh38.p7	16:74628524	AGCCCCCTGGCTCCA[A/C]GGGCAGCACATGAGG	55159
rs779833015	in-del	-/G	2.20885e-05	0.00332321	intron-variant	RFWD3	GRCh38.p7	16:74637975	CAGTAGGGAACTAGA[-/G]GGGGGAAAGCCAGCA	55159
rs779878514	snp	C/T	1.65425e-05	0.00287593	synonymous-codon	RFWD3	GRCh38.p7	16:74628645	AGCTCTGGGCATGTA[C/T]GACAGGGAGACCAGT	55159
rs780002331	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646507	AAAAAGAATTAATTC[A/G]CTGGGCGCAGTGGCT	55159
rs780150170	snp	G/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622037	AACGTCCCTCATAGT[G/T]AAGTCTCTTGCTTCC	55159
rs780152197	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74654298	CTCTCATTTTTCTAT[A/T]CTCTATTTCATTTAT	55159
rs780154986	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	RFWD3	GRCh38.p7	16:74661237	CAGTTGCGGAGCAGG[C/T]TGGAGCAGGGGTGGT	55159
rs780239953	snp	A/C			missense	RFWD3	GRCh38.p7	16:74652095	GGTCCTGCTCACCTG[A/C]AAGTAAGCATCCAAT	55159
rs780266882	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74644339	AAGGGAACATTCCAG[A/C]CAGGCATACTCTTAC	55159
rs780284858	snp	A/G	1.65181e-05	0.00287381	synonymous-codon	RFWD3	GRCh38.p7	16:74661312	GGATGGTACCCCCTG[A/G]CTGCTGACCACATCA	55159
rs780286619	snp	A/G	3.3157e-05	0.00407154	missense	RFWD3	GRCh38.p7	16:74644714	CAGAAGGTAGCAGAG[A/G]CTCAGACTTCTGGGG	55159
rs780338584	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74654269	AAGAACCAACTTTTT[G/T]ATTCGTTCATTTTCT	55159
rs780343181	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74625312	GACTGCTTGAGCCCA[A/G]GAGTTTGAGACCAGC	55159
rs780350746	snp	C/T	1.64738e-05	0.00286995	missense, intron-variant	RFWD3	GRCh38.p7	16:74630862	GAACCATTGGCCAGT[C/T]CAGCATAGATGTAGT	55159
rs780439660	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74624763	CACTTTGGGAGTCTG[A/C]GATGGGAGGACAGCT	55159
rs780441302	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74649274	AGGTATGAGAAGCTA[C/G]CAGGAGAGAGCCTGA	55159
rs780532742	snp	A/T	1.72359e-05	0.00293558	missense	RFWD3	GRCh38.p7	16:74637869	ACCTGAACACGCCTT[A/T]GAAGCCTAGTGCACT	55159
rs780585237	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660449	CAGAGTGAGACGCTG[C/T]CTCAAAAACAAAAAC	55159
rs780623055	snp	A/G	1.64787e-05	0.00287038	synonymous-codon	RFWD3	GRCh38.p7	16:74660982	TGCCCTCCGTGAAGC[A/G]GATACCCTCCTTCTT	55159
rs780636645	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630277	ACATTTTTTTGTATT[C/T]TCAGTAGAGACGGGG	55159
rs780638853	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74633685	CCAAGCATGGTAGCT[C/T]GCGCCTGTAATCCCA	55159
rs780642947	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74645264	AAGTGGCACACATTT[C/G]TGGAGCACCATTTGG	55159
rs780735281	snp	C/T	1.74133e-05	0.00295065	intron-variant	RFWD3	GRCh38.p7	16:74631004	ATTAAGAAAATCAAA[C/T]ACATGACAAAGATGT	55159
rs780738427	snp	C/T	4.94205e-05	0.0049707	intron-variant	RFWD3	GRCh38.p7	16:74644331	TGAACCAAAAGGGAA[C/T]ATTCCAGCCAGGCAT	55159
rs780757047	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74642029	TACATATATAGCTAA[C/T]CAAATACATAATAAC	55159
rs780771060	snp	A/G	3.31192e-05	0.00406921	intron-variant	RFWD3	GRCh38.p7	16:74632488	TACTCAACACCAAAG[A/G]GCCCAGTCTCCACCT	55159
rs780800619	snp	A/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668186	CCCATAGCTGAAACT[A/G]TAATTGCTTCAAACA	55159
rs780813920	snp	C/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623095	TCCTGGCAAGAGATA[C/G]TGTTCTTCAAAGCAC	55159
rs780845024	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642817	TCAAAAAGGCTCAAA[A/G]CAATATGGCAAAACA	55159
rs780913159	snp	C/T	3.29571e-05	0.00405924	missense	RFWD3	GRCh38.p7	16:74636361	CTGGAAGAAAAGAGG[C/T]CTGAGGAGAAGGCTG	55159
rs780920628	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74666288	ACTTTGGGCGGGTTT[C/T]CTAAACTCGGCTCAA	55159
rs780984179	snp	A/G	1.67041e-05	0.00288994	missense	RFWD3	GRCh38.p7	16:74661400	GCTGGCTGTTGTTCG[A/G]CATGATTTAACTGCA	55159
rs780988998	snp	C/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664335	CCCAAGCTACTTCTA[C/G]ATGTACTCAAGAGAC	55159
rs781011921	snp	C/T	6.58892e-05	0.00573936	missense	RFWD3	GRCh38.p7	16:74636445	CTGCCTGAGATACTG[C/T]GAAGGTCTTTTGGAA	55159
rs781036910	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74628026	CTGGCTGGGCACACA[C/G]AGCCACTGTTGTCCA	55159
rs781194022	snp	C/T	1.66266e-05	0.00288323	intron-variant	RFWD3	GRCh38.p7	16:74628692	AGTAAGGAAACTGTA[C/T]CTCACACTCCAAAAC	55159
rs781201791	snp	C/T	4.94246e-05	0.0049709	synonymous-codon	RFWD3	GRCh38.p7	16:74661225	CAGGTCAACAGACAG[C/T]TGCGGAGCAGGCTGG	55159
rs781217983	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74659503	AGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC	55159
rs781246262	in-del	-/CT	1.65848e-05	0.00287961	intron-variant	RFWD3	GRCh38.p7	16:74632480	TCCATGCTACTCAAC[-/CT]ACCAAAGAGCCCAGT	55159
rs781279588	in-del	-/GA			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664725	TGCACTCCAGACCGG[-/GA]GAGAGAGAGTAAGAC	55159
rs781337779	in-del	-/GTCCTTACCTATG	1.64741e-05	0.00286998	intron-variant	RFWD3	GRCh38.p7	16:74644520	TTAACATGTTAATGT[-/GTCCTTACCTATG]GTCCTTACCTGGGGA	55159
rs781399677	snp	A/G	1.74616e-05	0.00295474	missense	RFWD3	GRCh38.p7	16:74637864	AACGTACCTGAACAC[A/G]CCTTTGAAGCCTAGT	55159
rs781403227	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74634843	GGGCGCAGGTATAGG[C/G]TTTAAATCAACAAGG	55159
rs781418355	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656498	TCTTTTTTTTTCTTT[C/T]TGGAGACAGGGTCTG	55159
rs781458186	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74661558	GTTTAATATCATTCT[C/T]AGCAAGACTGAGAAG	55159
rs781489396	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74635636	ATTAGGAAATAGCTA[C/T]TTTTCCAATTTGTTG	55159
rs781492975	snp	A/G	1.93078e-05	0.00310701	intron-variant	RFWD3	GRCh38.p7	16:74636580	GTTTTTGCAAGTCCT[A/G]AAATGAAAAAGATTT	55159
rs781495740	snp	C/G	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74661131	TGGTGTGATTACCAT[C/G]AGATCCCTGCCTATG	55159
rs781508156	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645407	CTGAGAAATGCGTCT[C/T]TAGGCGATTTCGTCA	55159
rs781518976	snp	A/G	1.65323e-05	0.00287505	intron-variant	RFWD3	GRCh38.p7	16:74626314	GCAAAACTACTTTTT[A/G]TATGAAAGTAAAAAA	55159
rs781525154	snp	A/C/G			intron-variant	RFWD3	GRCh38.p7	16:74653101	CCTAGCACTTTGGGA[A/C/G]GCCAAGGTGGGTAAA	55159
rs781526832	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74640916	TGCACTCCAGCCTGG[A/G]CGACAGAGCGAGACT	55159
rs781579573	snp	A/G/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662390	AGTTATTAAGCACCT[A/G/T]TTATGCAGACAAGAC	55159
rs781602128	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74665753	TCTTTCTTTCTTTCT[-/T]TTCTTTTTTTGAGAT	55159
rs781708043	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74650354	GAGTAGATTCAGGGC[-/T]TTTTTTTTTTTTTGG	55159
rs781740786	snp	A/C/T	4.94298e-05	0.0049712	missense	RFWD3	GRCh38.p7	16:74652013	CAGAACTACTAGACA[A/C/T]CTGCAACTCTTCAGA	55159
rs781771453	snp	C/T	1.64863e-05	0.00287104	synonymous-codon	RFWD3	GRCh38.p7	16:74651924	AAAATACTGACCTTC[C/T]AAAATGACAGCTCCA	55159
rs796149696	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74633348	AATGAAGAGAAGAAG[-/A]AAAAAAAAAAGAAAA	55159
rs796224631	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74657934	GGGTGTTGACACGTA[C/T]ATCAATAGAATTCTA	55159
rs796390296	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658232	TTGTGATCTGTGTTA[C/T]TCACCAATATATCTA	55159
rs796537486	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74635483	AAAGAAAAAAAAAAA[-/A]TCAACAAGGTAACAG	55159
rs796569665	in-del	-/TC			intron-variant	RFWD3	GRCh38.p7	16:74657477	CCCAGGTTTTCTTTT[-/TC]TTTTTTTTTTTTTTT	55159
rs796638705	in-del	-/AAAAAA			intron-variant	RFWD3	GRCh38.p7	16:74633280	AAAACTCCGTCTCAG[-/AAAAAA]AAAAAAAAGAAAAGA	55159
rs796790831	in-del	-/A			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622469	TATTTCTACAAAAAA[-/A]TTTAAAAAAGGAAAA	55159
rs796849805	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74655555	CCCAGCTGAAGCCGA[C/T]GCTCTTTTACTGTTC	55159
rs796872698	in-del	-/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662907	GAATGGTCATGCTTC[-/T]TTTTTTTTTTTTTTT	55159
rs796922216	in-del	AA/G			downstream-variant-500B	RFWD3	GRCh38.p7	16:74620990	TAAAAAAAAAAAAAA[AA/G]AAAAAGGCCGGGTGC	55159
rs796927204	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635183	TACTCAGGAGGCTGA[A/G]GCAGAATGGCATGAA	55159
rs796962327	in-del	-/AGA			intron-variant	RFWD3	GRCh38.p7	16:74666196	ATTAGATAGATAGAT[-/AGA]TAGATAGATAGATAG	55159
rs797014837	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74640162	TTTTTTTTTTTTTTT[-/T]GAAACAGTCTTGCTC	55159

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