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

RLIM

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs770833560	in-del	-/TGAATAC			intron-variant	RLIM	GRCh38.p7	X:74600231	ATAATACTTGAAACT[-/TGAATAC]TTGACACTAGAAATC	51132
rs770853723	in-del	-/TTGT			utr-variant-3-prime	RLIM	GRCh38.p7	X:74589668	ATTCCTAAAGCAGAC[-/TTGT]TTATTTTGTAGAGTA	51132
rs770889641	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74599664	TATGAGGAATTGGGC[C/T]CTCAACATATATCAA	51132
rs770926248	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74610354	CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA	51132
rs770973421	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74584924	AAACTATCCTGAGAA[A/G]CCGAGTTATGATGCC	51132
rs770998427	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74610701	TCGAGACCAGCCTGG[C/T]CAATATGGTGAAACC	51132
rs771072717	snp	G/T	0.00021014	0.0102482	missense	RLIM	GRCh38.p7	X:74593023	TAAGCCAGTCTATTA[G/T]AGAGTCACCATTAGA	51132
rs771162253	snp	A/G	2.28071e-05	0.00337684	synonymous-codon	RLIM	GRCh38.p7	X:74592805	TTGCCTTTGGCTGTT[A/G]TTTTCCACATTTTCT	51132
rs771232607	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74610485	AAAAAAAAAAACCCT[C/T]GTGTTGGAACATTAA	51132
rs771274398	snp	A/G	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74594997	GAGACTCAGGCGGAA[A/G]AATCCCTTGAGTCCA	51132
rs771293791	in-del	-/A	0.0068637	0.0581785	upstream-variant-2KB	RLIM	GRCh38.p7	X:74614768	CGGGCGGCGGTTTGG[-/A]AAAAGGAAAGCTGTT	51132
rs771322184	snp	C/T	2.33011e-05	0.00341321	synonymous-codon	RLIM	GRCh38.p7	X:74591800	TCGCCTGGCACCTGA[C/T]GAGCCTGATGATGAG	51132
rs771443710	snp	G/T	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74614849	TGGCGAGAAATTTGC[G/T]TTCTGAGAATTGTGG	51132
rs771591020	snp	A/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74589894	TAAGAAACCAACATA[A/T]AGTGCATGTCCATAG	51132
rs771628103	snp	A/G	0.00158814	0.0281345	intron-variant	RLIM	GRCh38.p7	X:74613976	AGCATCTCACTTGGG[A/G]CAGCCTGATTTTTTA	51132
rs771648855	snp	C/T	2.28079e-05	0.00337689	synonymous-codon	RLIM	GRCh38.p7	X:74592223	ACGTGAAAATGTACG[C/T]CTAAAACCTCCTCGT	51132
rs771668702	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74589286	AAGAAAATTGATTTG[C/T]TTTTAGCCAATCAAG	51132
rs771723868	snp	G/T	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74600116	GAAATGTGGTGGTGG[G/T]GGGGAGATCATAATA	51132
rs771804953	snp	C/T	0.00158814	0.0281345	intron-variant	RLIM	GRCh38.p7	X:74610191	GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC	51132
rs771806629	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74601845	TTCTGATTCAGTAGA[C/T]TGGGGTAGGGCCTGA	51132
rs771823704	snp	G/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583819	GTGGGAGGCCGAGAC[G/T]GGCAGATCATGGGAT	51132
rs771859958	in-del	-/T	0.0026455	0.0362733	intron-variant	RLIM	GRCh38.p7	X:74609128	GTAACTAAGGCACTA[-/T]TTTTAAGGACCTAAG	51132
rs771903889	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74603175	GTCTTCTATTCTGGG[A/C]TTAGGGTCATAGTAA	51132
rs772018102	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583316	CAGCCATTCACCCAA[C/T]ATTTGCTTTTGCTCT	51132
rs772056392	snp	A/G			downstream-variant-500B	RLIM	GRCh38.p7	X:74582598	ATTGTCATAATTGGG[A/G]CCAAGAGCACACGTA	51132
rs772104639	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74594557	GAGTAGGTAGGTCCT[A/G]GGAAAAATTCACTTC	51132
rs772114185	in-del	-/G			intron-variant	RLIM	GRCh38.p7	X:74608446	AAAAAAAAAAAAAAA[-/G]AACAGGCAGGGTTAA	51132
rs772231550	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74594959	CGCACAGTGGTACCA[C/T]ATCTGTAGTGCCAGC	51132
rs772284725	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74596867	AAACTGAGTATACAC[C/T]CATCATCTCAAACAA	51132
rs772284810	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74611867	CATTCTCATGAGGCT[C/T]TGTTGTGAGAATTAT	51132
rs772309563	snp	A/C	0.00105904	0.0229869	utr-variant-3-prime	RLIM	GRCh38.p7	X:74586006	CTTCAGAAAGCTTTC[A/C]AAGATTGCTGCCCTG	51132
rs772324845	snp	C/T	2.2798e-05	0.00337616	missense	RLIM	GRCh38.p7	X:74592783	ATTCAGATCGTGGGT[C/T]TTCCACTTGCCTTTG	51132
rs772360939	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74585131	TTTTGTATATATACA[A/G]GGCAAGCAAGGGAGT	51132
rs772364567	snp	A/T	2.28611e-05	0.00338083	missense	RLIM	GRCh38.p7	X:74591512	GGTAGAATTCTCAGA[A/T]AACCAGCGATCGATG	51132
rs772434405	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74606112	ATGAAAAATTCCAAA[A/G]TGACAAAACACCTTT	51132
rs772437962	snp	C/G			intron-variant	RLIM	GRCh38.p7	X:74608757	AAACGCTCTAAAACA[C/G]TTAAAACTGAAAGAG	51132
rs772456425	snp	A/G	2.34203e-05	0.00342193	synonymous-codon	RLIM	GRCh38.p7	X:74595882	ATTTACAAATTGATA[A/G]AAAGCTTCTTCTCGA	51132
rs772483537	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74599355	TCTAAAATACAGGGA[A/G]ACTACAAACAAAAAT	51132
rs772523678	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74588258	GCACATCACTTGAGG[C/T]CAGGAGTTCAAGACC	51132
rs772553546	snp	A/C	0.00528398	0.051128	intron-variant	RLIM	GRCh38.p7	X:74607052	TGTGGCTGAGGTGGG[A/C]GGATCACTTGAGTTT	51132
rs772631689	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74610348	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	51132
rs772794897	snp	C/T	4.95681e-05	0.00497811	intron-variant	RLIM	GRCh38.p7	X:74594268	AAGTTCCTATCATCC[C/T]ATCGTCTATCCACCT	51132
rs772883773	snp	A/C	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74597969	AATTAGTGTTTCCTG[A/C]AGACTTGATAATGTT	51132
rs772945830	snp	C/T	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74608124	GAAATCCAGTCTTGG[C/T]TGTAACTTGGTTATG	51132
rs772945878	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74597240	AGAAGCTGAAGAAAT[A/G]TGTCCAGAGAAAATA	51132
rs772950727	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74601856	TAGATTGGGGTAGGG[A/C]CTGAGATTCTGCATT	51132
rs773064089	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74590607	CTTACAAAAGCAGCT[C/T]TGTACTTTGTTTGGT	51132
rs773223009	in-del	-/AACA			utr-variant-3-prime	RLIM	GRCh38.p7	X:74587571	AAAAGAAAAAATATT[-/AACA]ACCATAAGGTGCCAC	51132
rs773234133	snp	C/T	0.000160567	0.00895867	missense	RLIM	GRCh38.p7	X:74591958	TGGAACCAGAACTAC[C/T]ACCACCACCAGAACC	51132
rs773314309	snp	G/T			intron-variant	RLIM	GRCh38.p7	X:74612904	CAGACCAGTAATTAT[G/T]TTCAGATTCTGATAG	51132
rs773319150	snp	A/G	0.0026455	0.0362733	intron-variant	RLIM	GRCh38.p7	X:74609405	AAGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	51132
rs773324210	snp	C/G	1.64741e-05	0.00286998	stop-gained	RLIM	GRCh38.p7	X:74591858	TCTGAGCTAGTTTCT[C/G]AACTTTCACCACCGG	51132
rs773335683	snp	A/T	4.56178e-05	0.00477565	synonymous-codon	RLIM	GRCh38.p7	X:74592682	TGGGCTCCTGCTTCT[A/T]GCCCTCCTCTGACCT	51132
rs773367937	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74594038	GAATAAATTTCAATG[A/G]AGGTGAAAAACAAAC	51132
rs773371272	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74597005	ATACTAAATACAATA[C/T]ATACTGACACTATTA	51132
rs773419484	snp	A/G	0.00317376	0.039709	intron-variant	RLIM	GRCh38.p7	X:74594927	AAAAAAAAAGGCAAA[A/G]GCAATTCTAAGCTGG	51132
rs773420844	in-del	-/TA	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74603505	TATATTTTTGAAGTG[-/TA]TATGTGTCTTCTCTT	51132
rs773502143	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583464	CCCGCAGCATATTTA[C/T]ACTGTGGAACGGTGC	51132
rs773544351	in-del	-/AG	0.017851	0.0927731	intron-variant	RLIM	GRCh38.p7	X:74604448	ATTTCTTTGTAAGAT[-/AG]AGAAATCCCAAATAG	51132
rs773567405	snp	C/T	4.56376e-05	0.00477669	synonymous-codon	RLIM	GRCh38.p7	X:74591542	GCAGTGGACATGGTA[C/T]TCATGGGAACAAGGT	51132
rs773584660	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74588407	ACCCAGGAGGCAGAG[A/G]TTGCAGTGAGCCGAG	51132
rs773617357	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74590048	TGAGATGTTAGGACT[A/G]TGTTAGAGATAGTAA	51132
rs773622408	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74608819	AGACCATGCCAAATG[C/T]GGTTGATCTACAGGA	51132
rs773657198	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74613187	TAATGGGGTGATAAG[C/T]AGTTACTCTGTCTAT	51132
rs773678363	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74588228	TAATCCCAGCATTTT[C/T]GGAGGCCGAGGCAGG	51132
rs773722439	in-del	-/A			intron-variant	RLIM	GRCh38.p7	X:74613983	ACTTGGGGCAGCCTG[-/A]ATTTTTTACTTCCCT	51132
rs773731548	snp	C/G	2.33743e-05	0.00341857	missense	RLIM	GRCh38.p7	X:74591828	GAGCTTCCTTCATTA[C/G]TGCCTTCAAATAAAT	51132
rs773740166	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74588331	TAAAAACTAGCCAGG[C/T]GTGGTGGCATGCGCC	51132
rs773807386	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74598711	ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC	51132
rs773824862	snp	G/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74613261	TATTTCTTCCCCCTT[G/T]CAATCAGTCCAAAAC	51132
rs773922290	snp	G/T			synonymous-codon	RLIM	GRCh38.p7	X:74591926	ACTGGAACTCGAACT[G/T]GAACTGGAACTCGAA	51132
rs773935959	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74609105	AACTGACAATGTTGG[A/T]GTTCATCAGTAACTA	51132
rs774073423	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74599888	AACACCTGAAGTGCC[A/G]GAATGTTCACAATTC	51132
rs774080177	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74587677	ATTTTGGGAACTGAC[C/T]GAAAGTCATGGCTGA	51132
rs774103461	snp	A/C/G	0.000321196	0.0126689	missense	RLIM	GRCh38.p7	X:74591939	CTGGAACTGGAACTC[A/C/G]AACTGGAACCAGAAC	51132
rs774107211	snp	C/T	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74598109	CTGTTTTATATACTT[C/T]ATGTCCTGACAAAGT	51132
rs774162251	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74608332	TAACTAGGACATAAG[C/T]TTATAAGCTCTGCTT	51132
rs774203715	snp	A/C	0.000136919	0.0082729	missense	RLIM	GRCh38.p7	X:74592562	TACCAAAGGATGTTC[A/C]AAAGTCTGAGATGAG	51132
rs774205613	in-del	-/GAA	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583216	GAGACTTGAGCATAT[-/GAA]GAAGTTCTGAATTAT	51132
rs774267584	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74601757	TGCACAGGATCTGAG[A/G]TTTTTCTTCCTATTA	51132
rs774280088	snp	G/T	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74616162	TGTTTACTTCACCCT[G/T]TCTGAGCAGTAAACC	51132
rs774339849	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74593668	AGTCTGAACCTTGCA[A/T]AGCACATATAATGGC	51132
rs774462500	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74600726	CTTTAACAATAGTAT[C/T]GGGGGCTGGGTGCAG	51132
rs774464973	snp	A/G	2.34588e-05	0.00342474	synonymous-codon	RLIM	GRCh38.p7	X:74595954	ATCACCACTTCCTTT[A/G]TCATTGGAATCTGAG	51132
rs774484293	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74584027	TCCAGCCTGGGCGAC[A/G]GGGCGAGAATCCATC	51132
rs774602262	snp	A/G	0.000165442	0.00909359	missense	RLIM	GRCh38.p7	X:74595961	CTTCCTTTGTCATTG[A/G]AATCTGAGTTTTCCA	51132
rs774630397	snp	A/G			upstream-variant-2KB	RLIM	GRCh38.p7	X:74614648	GGAAGTGATGATGCC[A/G]CGTCCCGGCACCGCA	51132
rs774696272	snp	C/T	2.36298e-05	0.0034372	intron-variant	RLIM	GRCh38.p7	X:74594417	ACCACAGGGCAAAGA[C/T]GACATTAGGGGTATG	51132
rs774710317	in-del	-/AT			utr-variant-3-prime	RLIM	GRCh38.p7	X:74590149	CCTATTAACACACAC[-/AT]GTGTACCAACTGCAA	51132
rs774727031	snp	G/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74595000	ACTCAGGCGGAAGAA[G/T]CCCTTGAGTCCAGCC	51132
rs774830154	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74604995	AAGCCTCCATCCTTT[C/T]TGCCTTAACTTAGCA	51132
rs774855074	snp	A/C	2.31107e-05	0.00339924	missense	RLIM	GRCh38.p7	X:74595922	TCCATCTGACTTCTG[A/C]GCTGTGCTGCAGACT	51132
rs774958959	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74614023	CCCAAGCCCGCCATG[A/G]AAAACGCGGGGAGGT	51132
rs774991596	in-del	-/AA			upstream-variant-2KB	RLIM	GRCh38.p7	X:74615820	TCTTTTCCTTTTCCC[-/AA]TTTTTCTGTTTTCCA	51132
rs774993535	snp	C/T	0.00158814	0.0281345	intron-variant	RLIM	GRCh38.p7	X:74613970	GTTGCCAGCATCTCA[C/T]TTGGGGCAGCCTGAT	51132
rs775020802	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74586824	TAAGGCTGGGCGCAG[C/T]GGCTCACGCCTATAA	51132
rs775051047	snp	A/G	4.58001e-05	0.00478518	synonymous-codon	RLIM	GRCh38.p7	X:74591623	GGTTTTTAATGCATC[A/G]TTTTCACCAAAACTT	51132
rs775063509	snp	A/G	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74600153	GAGTTTCTTAATCTC[A/G]TAACTGAGATTGCTT	51132
rs775086129	snp	C/G			intron-variant	RLIM	GRCh38.p7	X:74605871	ACAAACAGAAGCACA[C/G]AGAAAGAAAGTGATT	51132
rs775163098	snp	C/G	2.33171e-05	0.00341438	missense	RLIM	GRCh38.p7	X:74591805	TGGCACCTGATGAGC[C/G]TGATGATGAGCTTCC	51132
rs775255125	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74588803	GGATGTGGGTGGGGG[A/G]AAAACGATTTTTGTT	51132
rs775255635	snp	A/T			intron-variant	RLIM	GRCh38.p7	X:74597171	GGCTCATTTATTGGC[A/T]AAACGAGGAAAGCTG	51132
rs775262415	snp	C/G	2.28543e-05	0.00338033	missense	RLIM	GRCh38.p7	X:74592467	GCTGCAAAAAGACCT[C/G]TACTTAGCAACTCAG	51132
rs775342071	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583383	TCCTGACCTTGTACA[C/T]GAATAGCAGGCTGTT	51132
rs775435635	snp	A/C	2.39811e-05	0.00346265	intron-variant	RLIM	GRCh38.p7	X:74594438	TAGGGGTATGACAAT[A/C]AAATACTTTATCAGT	51132
rs775470432	in-del	-/CT			utr-variant-3-prime	RLIM	GRCh38.p7	X:74591077	TAATTTCCTTTGCTC[-/CT]CTCTTATGGTGTGGG	51132
rs775471649	in-del	-/AAC	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74608583	TGCTCATGCTACCAT[-/AAC]AATAAGAGATTATAA	51132
rs775517020	snp	C/G			intron-variant	RLIM	GRCh38.p7	X:74599740	GAAAGATATGTTTTT[C/G]TTGTTTATAAGCCAC	51132
rs775519993	in-del	-/GAACTGGAACTGGAACTC	0.000910747	0.02132	cds-indel	RLIM	GRCh38.p7	X:74591903	CTGGAACTGGAACTT[-/GAACTGGAACTGGAACTC]GAACTGGAACTGGAA	51132
rs775546104	snp	C/T			intron-variant, utr-variant-5-prime	RLIM	GRCh38.p7	X:74612635	GATTTTAGTTTTCTT[C/T]ACTCTGCTCTAGAAA	51132
rs775567458	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583840	ATCATGGGATCAGGG[A/G]TTCAAGACCAGCCTG	51132
rs775635210	snp	C/T	4.56699e-05	0.00477838	synonymous-codon	RLIM	GRCh38.p7	X:74592283	TGTCTGAGACCTAGA[C/T]CGAGTTCTGCTGGCT	51132
rs775700963	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74610882	GCGACAGAGTGAGAC[C/T]CCGTCTCAAAAAAAT	51132
rs775727162	snp	C/G	0	0	utr-variant-3-prime	RLIM	GRCh38.p7	X:74586071	AAGCAGCTCTTCCTG[C/G]GAGAAGATAAAACAG	51132
rs775741001	snp	A/G	0.00581083	0.0535878	intron-variant	RLIM	GRCh38.p7	X:74602604	TATCTGGGCGTGGTG[A/G]CGCATGCCTGTAGTC	51132
rs775748062	snp	G/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74590682	CTAAGCATGGTACTT[G/T]ACAATTTTTAATGCA	51132
rs775794183	snp	A/C	0.0026455	0.0362733	intron-variant	RLIM	GRCh38.p7	X:74601518	CTTAAAAAAATACAA[A/C]CCCCCCCCCAAAAAG	51132
rs775800023	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74611870	TCTCATGAGGCTCTG[C/T]TGTGAGAATTATAAA	51132
rs775853886	snp	C/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74596859	ATTAAAAAAAACTGA[C/G]TATACACTCATCATC	51132
rs775856503	snp	C/T	4.74254e-05	0.00486934	intron-variant	RLIM	GRCh38.p7	X:74594423	GGGCAAAGATGACAT[C/T]AGGGGTATGACAATC	51132
rs775907099	snp	A/G	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74596181	GTCAAGGGTTGGCAA[A/G]CTACAGCCCTTGAAC	51132
rs775913456	snp	A/G	2.28094e-05	0.00337701	synonymous-codon	RLIM	GRCh38.p7	X:74592814	GCTGTTGTTTTCCAC[A/G]TTTTCTCCACTAGAA	51132
rs776065494	snp	G/T			intron-variant	RLIM	GRCh38.p7	X:74602031	GCCCTGTAAACTTTA[G/T]CATTTTTAAATGAAC	51132
rs776122113	snp	C/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74606151	GCACAAACCTAGATG[C/G]ACTTATTTTTAAATA	51132
rs776176106	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74604447	TATTTCTTTGTAAGA[C/T]AGAGAAATCCCAAAT	51132
rs776212774	snp	G/T	2.32585e-05	0.00341009	synonymous-codon	RLIM	GRCh38.p7	X:74595894	ATAGAAAGCTTCTTC[G/T]CGATCCAATCGGTCC	51132
rs776219235	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74585741	GAGTCTGCTGGATAG[A/G]TATCGGAGAAGGGTG	51132
rs776252280	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74607363	CACAAAAATGTGTCA[C/T]ACTGACAAGAGAAGG	51132
rs776284681	snp	C/T	4.58658e-05	0.00478861	missense	RLIM	GRCh38.p7	X:74591987	CCTCCTCTTCCACTC[C/T]GTGACTCTGCCCTTT	51132
rs776318692	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74590421	ACTTTAAATTCTTCA[A/G]TTTTCTTTACTCCTC	51132
rs776372104	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74615745	ATTGAGGGAACTCGC[C/T]ACACAGCATGCCACT	51132
rs776408104	snp	A/C			upstream-variant-2KB	RLIM	GRCh38.p7	X:74614878	GGGAACCTTCGCTTT[A/C]CCATTTTGAAAACTG	51132
rs776494746	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74600275	AAACACGCACAAAAA[A/T]CAGGCACTAAAAAAA	51132
rs776676399	snp	C/T	9.12763e-05	0.00675498	missense	RLIM	GRCh38.p7	X:74592260	TCATAGGTGACAGTG[C/T]TGTTTGGTGTCTGAG	51132
rs776736303	in-del	-/G			intron-variant	RLIM	GRCh38.p7	X:74613543	GGAAAAAGGGACCGA[-/G]TATTCAGGAAGCAGA	51132
rs776745228	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74610591	CCCAATTGAGGTATA[C/T]TTAAAAAATACCTCA	51132
rs776837507	in-del	-/C	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74612020	GGAATTATTAATGTT[-/C]CCTTTTGTTCTTAAA	51132
rs776855075	snp	A/C	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74603374	CCCTTAAAGATCCAA[A/C]GAGATCTTCCCTCCT	51132
rs776855421	in-del	-/GAACTC	2.65045e-05	0.00364026	cds-indel	RLIM	GRCh38.p7	X:74591915	CTTGAACTGGAACTG[-/GAACTC]GAACTGGAACTGGAA	51132
rs776858201	in-del	-/GAG			utr-variant-3-prime	RLIM	GRCh38.p7	X:74583332	TTTGCTTTTGCTCTT[-/GAG]GAGGGGCAGATGCCA	51132
rs776882531	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74587154	CGGATCTTTTACTTT[C/T]TTCCAAATGAAGTAT	51132
rs776926973	snp	G/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74590415	AGGAAAACTTTAAAT[G/T]CTTCAGTTTTCTTTA	51132
rs776938065	snp	A/G	0.00150354	0.0273771	missense	RLIM	GRCh38.p7	X:74592716	GTAGGTGGGACCTCT[A/G]TTAACGCTTCAGTTG	51132
rs777113217	in-del	-/AT			intron-variant	RLIM	GRCh38.p7	X:74603714	GATACAATTTGAACC[-/AT]ATATGTAATTTTTCA	51132
rs777266242	snp	A/C	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74583637	TTACAAGGTACACTT[A/C]AACTGCTAAAATGAT	51132
rs777281271	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74593707	GAACCAAATTATTAT[C/T]GTAGCCTCTCAGGTT	51132
rs777314427	snp	A/G	2.28014e-05	0.00337641	synonymous-codon	RLIM	GRCh38.p7	X:74592703	CCTCTGACCTCTGGT[A/G]GGTGGGACCTCTGTT	51132
rs777371179	snp	C/G			intron-variant	RLIM	GRCh38.p7	X:74603306	GCTTTACCACCGTCA[C/G]AATGTACTGCTATTC	51132
rs777399262	in-del	-/AAAAAAAAAAA			intron-variant	RLIM	GRCh38.p7	X:74609488	GCGAGACTCCGTTTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA	51132
rs777427090	snp	C/T	2.28144e-05	0.00337738	missense	RLIM	GRCh38.p7	X:74592236	CGCCTAAAACCTCCT[C/T]GTTCACTTTCATAGG	51132
rs777440051	snp	C/T	0.000115655	0.00760356	synonymous-codon	RLIM	GRCh38.p7	X:74594328	TTCATCTGAGTTTTG[C/T]GGTGGTGGGCCTTCT	51132
rs777505594	in-del	-/TAAGA			intron-variant	RLIM	GRCh38.p7	X:74600084	CCTATCTTGTTTAAT[-/TAAGA]TGAGTATGTCAAGAA	51132
rs777617647	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74608197	TCCATCAATATTAGA[A/G]TATTGGATTAAACCA	51132
rs777625104	snp	C/T	2.28762e-05	0.00338195	synonymous-codon	RLIM	GRCh38.p7	X:74592427	TGAAGAACCTGCTCC[C/T]TGAGAAGCATTTCTT	51132
rs777739893	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74585145	AGGGCAAGCAAGGGA[A/G]TGGTCAGAGCAATGG	51132
rs777759324	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74605356	TGCAAACAAACATTT[C/T]AAAGTTTAGGCATGC	51132
rs777788614	in-del	-/T	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74612524	ATAGAACAATAAATA[-/T]TTGTAAACATGCATT	51132
rs777909931	snp	A/G	0.00105904	0.0229869	upstream-variant-2KB	RLIM	GRCh38.p7	X:74615384	GGGTGACAGAGCAAG[A/G]CTGTGTCTCAAAAAA	51132
rs777919352	in-del	-/C	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74611743	AACCCAGAAGTATAA[-/C]GTCAGACAGGCCTGG	51132
rs777927809	snp	A/G	0.0068637	0.0581785	intron-variant	RLIM	GRCh38.p7	X:74606871	CCGAGTGTGGTGGCC[A/G]ACATCTGTAATCCTA	51132
rs777933655	snp	A/G	0.00317376	0.039709	intron-variant	RLIM	GRCh38.p7	X:74612186	CACACACAAAGTAAC[A/G]TAAAATTATACTCTC	51132
rs778007999	snp	C/T	2.2905e-05	0.00338408	missense	RLIM	GRCh38.p7	X:74592990	TTCTTGTTGTATTTC[C/T]AGTTTGTCTGACAGA	51132
rs778076289	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74613635	AGCAGAGACCCCCCT[A/G]GGCTTTTTTTTTTTT	51132
rs778101815	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74601019	ACAAGAATGAAACTC[C/T]GTCTCAAAGGAAAAA	51132
rs778141103	snp	G/T			intron-variant	RLIM	GRCh38.p7	X:74599536	TTAGGAGGTAGGGCC[G/T]TTGGTCATAAGGGTG	51132
rs778209925	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74589167	TGGGAGATTAGGAAG[A/G]TACCTGTTGTCAATA	51132
rs778243260	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74590060	ACTGTGTTAGAGATA[A/G]TAATGAAATATGATC	51132
rs778270630	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74612178	TCAACCACCACACAC[A/C]AAGTAACGTAAAATT	51132
rs778307369	snp	C/T	2.32945e-05	0.00341273	synonymous-codon	RLIM	GRCh38.p7	X:74591782	GGCCCTATGTCGACC[C/T]TCTCGCCTGGCACCT	51132
rs778309571	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74610535	CAAAAATACCAACTA[C/T]ATATGTCAGGAGAAA	51132
rs778391559	snp	A/G	2.28035e-05	0.00337657	missense	RLIM	GRCh38.p7	X:74592206	ACACCTGCCCGCTCA[A/G]AACGTGAAAATGTAC	51132
rs778417221	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74599587	AACGCTTTTATAAAA[C/T]AGTCCCCAGAGAGTT	51132
rs778479669	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74591193	GATAAATTATCAGTA[A/G]CAGTGATGCTACCAA	51132
rs778506286	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74600082	ATCCTATCTTGTTTA[A/T]TTAAGATGAGTATGT	51132
rs778596143	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74594493	TGATTAGAAAAAAAA[A/T]CATATTTTTAAAAGA	51132
rs778771793	snp	C/T	0.000250664	0.0111924	synonymous-codon	RLIM	GRCh38.p7	X:74592925	GAAATCACCACTGTT[C/T]GGATTAGTCCGACTC	51132
rs778844566	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74603061	TCAAGCAGAAGCTGG[A/C]TATTAAAAAGAGGAT	51132
rs778867902	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74585959	AGCCTTTGTTACTGT[C/T]CCCCCTCCAAACCCC	51132
rs778870022	snp	C/G/T	9.50017e-05	0.00689143	missense	RLIM	GRCh38.p7	X:74591771	AATGTGACTGGGGCC[C/G/T]TATGTCGACCCTCTC	51132
rs778899408	in-del	-/ACAAA			intron-variant	RLIM	GRCh38.p7	X:74600291	AGGCACTAAAAAAAT[-/ACAAA]ACAAAACAAAACAAA	51132
rs778928501	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74587506	TAATTTTTTTTGTTC[A/G]CAAAAGAACAAAGGA	51132
rs779021988	in-del	-/T			intron-variant	RLIM	GRCh38.p7	X:74610897	TCCGTCTCAAAAAAA[-/T]AAAAAAATAAAAAAT	51132
rs779042764	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74613568	AGCAGAAGCCCAACC[A/G]GTTAATACTAGTTAC	51132
rs779102310	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74596773	CATTGCTTTGGACTG[C/T]TGCTCTGTGCACTCT	51132
rs779153874	snp	C/T	0	0	intron-variant	RLIM	GRCh38.p7	X:74607003	AGCTGGGCATGGTAA[C/T]GCGCATCTGTGGTCC	51132
rs779232269	snp	A/G	0.00738971	0.0603345	upstream-variant-2KB	RLIM	GRCh38.p7	X:74614775	GCGGTTTGGAAAAGG[A/G]AAGCTGTTATGACGC	51132
rs779244784	snp	A/T			upstream-variant-2KB	RLIM	GRCh38.p7	X:74615932	CTGGAATATTTTACT[A/T]TCATATCTTTGCTTT	51132
rs779301932	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74596586	TTGCAACCTAAGAAT[A/G]GTTTTTAGAGACTAT	51132
rs779328088	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74601204	TCAACTTCCATTTTG[C/T]TTCTATTTTATTCAA	51132
rs779352147	snp	C/T	2.53897e-05	0.0035629	utr-variant-5-prime	RLIM	GRCh38.p7	X:74596000	AACAAGTGGAAAATA[C/T]CTGAAAAGAGAAAAG	51132
rs779355492	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74599118	TTTTGTGTGACAATA[C/T]GCTCAATTTTGCTTT	51132
rs779367907	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74615523	AGTGATAAATGCCAA[A/G]GAGAAAAATCAAGGA	51132
rs779436315	snp	C/T	2.29917e-05	0.00339047	missense	RLIM	GRCh38.p7	X:74591490	CTGCTCTGCGACAAA[C/T]AGGACAGGTAGAATT	51132
rs779443798	snp	C/T	2.38149e-05	0.00345064	synonymous-codon	RLIM	GRCh38.p7	X:74595855	AAGCCTATAATCTTC[C/T]TCACTCAGGTTATTT	51132
rs779548303	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74590150	CTATTAACACACACA[C/T]GTGTACCAACTGCAA	51132
rs779564088	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74601796	TATAGACCAGTGTAA[C/T]AGGAATTATCTGGAA	51132
rs779613371	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74610971	GCTGGATTATCTGGG[A/G]AACTTTCATGTTTGA	51132
rs779617386	in-del	-/ATCT	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74601308	TAATTTCTAATGACA[-/ATCT]ATCTTTTGAGATGTC	51132
rs779619275	in-del	-/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74583365	ATGGAAACAGTCAAA[-/G]GTTCCTGACCTTGTA	51132
rs779639087	in-del	-/T	0.0126344	0.0784702	utr-variant-3-prime	RLIM	GRCh38.p7	X:74590204	AGTCTCTTTCCTCCA[-/T]TTTTTTCATTTTTGA	51132
rs779699116	in-del	-/A			intron-variant	RLIM	GRCh38.p7	X:74609488	GCGAGACTCCGTTTC[-/A]AAAAAAAAAAAAAAA	51132
rs779738459	snp	A/G	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74610618	CTCAATTGGCCAGTC[A/G]CGGTGGCTCACGTCT	51132
rs779851204	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74608360	CTTTTCTCACTACCA[C/T]TTCACTCAATGTACT	51132
rs779902507	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74609886	GAAGGGACCTTTTGT[C/T]ATTCCAGAAAAAAAT	51132
rs779955852	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74585595	CTATTAATAATCAAA[C/T]CAGCTTTAATATGAT	51132
rs780003677	snp	A/G	3.29484e-05	0.00405871	intron-variant	RLIM	GRCh38.p7	X:74595805	TAAATATATGTAAGC[A/G]TACCTGGGGTGCCTA	51132
rs780040980	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74604962	TCCCCATGATACTCC[C/T]GCAACACACTTATTT	51132
rs780071027	in-del	-/GG			intron-variant	RLIM	GRCh38.p7	X:74611608	CGTAACAGACGAAAA[-/GG]GGGGATTGCTGGATA	51132
rs780090338	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74605582	CAACATCATCGTAAA[A/G]GAGAAGGTCATAAAT	51132
rs780124512	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74588119	TCTATAGTGTTGATA[C/T]AAAGTCAGCAAACTT	51132
rs780135582	snp	A/C	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74598485	ATTAAATTAAATTAA[A/C]AGATAAAAAATTGCC	51132
rs780191156	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74594565	AGGTCCTGGGAAAAA[C/T]TCACTTCTTTGGAAA	51132
rs780218156	snp	A/G			upstream-variant-2KB	RLIM	GRCh38.p7	X:74615627	AACTCTAAAGTATTC[A/G]AAAAAGGGCGGTGAT	51132
rs780243906	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74584938	AACCGAGTTATGATG[C/T]CAATGACAGATAGCT	51132
rs780305319	snp	A/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74597789	GGTTTAAGCTCAAGT[A/T]CCATGAATTTTTGTC	51132
rs780313711	snp	A/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74612954	TGGCACATTACACTA[A/G]CCTAAGGTAGGAACT	51132
rs780347592	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74614107	TGACGCCTGAGGCCA[A/C]AACTCAAAAACTGCC	51132
rs780359137	snp	G/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74607127	AGTCTGGGTGACAGA[G/T]ACTCCATATCAAAAT	51132
rs780393532	snp	A/T	2.33465e-05	0.00341653	missense	RLIM	GRCh38.p7	X:74591749	GGGCAAAGAGCCACT[A/T]TCATCAAATGTGACT	51132
rs780412306	snp	A/G			intron-variant	RLIM	GRCh38.p7	X:74596529	TGGGATTACAGGCAT[A/G]AGCCACCGCACCCAG	51132
rs780484186	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74615700	AGGGCAGTTAAAGAA[A/G]GCCTTTCTTAGGTAG	51132
rs780526980	snp	A/G	0.000529661	0.016265	downstream-variant-500B	RLIM	GRCh38.p7	X:74582965	ACCTGGCATTTGCTC[A/G]GTACATACGGTTCAG	51132
rs780552003	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RLIM	GRCh38.p7	X:74616596	ATAAAATCATAAAAG[A/G]AGTGGAAGAAAATAC	51132
rs780562192	snp	A/G	0.000115939	0.0076129	synonymous-codon	RLIM	GRCh38.p7	X:74594379	CAGCAACTCTTCCTC[A/G]GTACTTTCACCTGAA	51132
rs780577646	snp	A/G	2.28896e-05	0.00338294	synonymous-codon	RLIM	GRCh38.p7	X:74592400	TGTAGATTCACCACT[A/G]GCAGCTGTGTCTGAA	51132
rs780619016	in-del	-/A			utr-variant-3-prime	RLIM	GRCh38.p7	X:74585953	AAGGCAGCCTTTGTT[-/A]ACTGTTCCCCCTCCA	51132
rs780660442	snp	C/T			intron-variant	RLIM	GRCh38.p7	X:74598845	CTAAAATCATACACT[C/T]GTGGATTGCTTAAGA	51132
rs780691503	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74593236	AAGAAAATTCTAATT[C/T]CATTTGAAAAGAGCA	51132
rs780820346	snp	G/T	0.000345359	0.0131362	synonymous-codon	RLIM	GRCh38.p7	X:74591908	ACTGGAACTTGAACT[G/T]GAACTGGAACTCGAA	51132
rs780876723	in-del	-/ATATA	0.00105904	0.0229869	intron-variant	RLIM	GRCh38.p7	X:74611311	GAAAAATTAATGTAC[-/ATATA]ATATAATTCCATAAA	51132
rs780930315	in-del	-/A			intron-variant	RLIM	GRCh38.p7	X:74597899	GGCAAAGATGGATTT[-/A]TTTTCTGTGAGAACC	51132
rs780933109	in-del	-/C	2.36155e-05	0.00343616	intron-variant	RLIM	GRCh38.p7	X:74594416	ACCACAGGGCAAAGA[-/C]TGACATTAGGGGTAT	51132
rs781027955	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74589077	TTATGAATAGCTTCA[A/G]TATCTACATTCATAG	51132
rs781070393	snp	A/T			intron-variant	RLIM	GRCh38.p7	X:74608255	ATCTGTAACTGTAAA[A/T]AAGATATAACCTACA	51132
rs781124103	snp	C/G	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74610666	GGAGGCCAAGGTGGG[C/G]AGATCACAAGGTCAG	51132
rs781137879	snp	C/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74586603	TTATACAGCTCAATT[C/G]TATGCTGCAGCCTTT	51132
rs781151753	snp	C/T	4.90316e-05	0.0049511	synonymous-codon	RLIM	GRCh38.p7	X:74591443	TTCAGATCTTAATTA[C/T]ACAACACTTTCTCTG	51132
rs781171855	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74587638	AGAGGAATTTTGCAA[C/T]CTTTACCTCCCTATC	51132
rs781259470	snp	A/G	0.0026455	0.0362733	utr-variant-3-prime	RLIM	GRCh38.p7	X:74589068	TTCCAGTGTTTATGA[A/G]TAGCTTCAATATCTA	51132
rs781260802	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74585746	TGCTGGATAGGTATC[A/G]GAGAAGGGTGTTATG	51132
rs781313029	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74599309	CTCATCAATGAACTG[C/T]ACACTAATAAAAAAC	51132
rs781317448	snp	C/G	0.000529661	0.016265	utr-variant-3-prime	RLIM	GRCh38.p7	X:74584714	CCCAAGTAGCTGGGA[C/G]CACAGCTGTGTACCA	51132
rs781417152	snp	C/T	2.29532e-05	0.00338763	missense	RLIM	GRCh38.p7	X:74591937	AACTGGAACTGGAAC[C/T]CGAACTGGAACCAGA	51132
rs781423745	snp	C/G	2.55575e-05	0.00357464	intron-variant	RLIM	GRCh38.p7	X:74593080	TTCAAAACAAAGGAG[C/G]GGGAGAGGGAGAAAA	51132
rs781518341	snp	C/T	0.00105904	0.0229869	utr-variant-3-prime	RLIM	GRCh38.p7	X:74588235	AGCATTTTCGGAGGC[C/T]GAGGCAGGCACATCA	51132
rs781548197	snp	A/C			intron-variant	RLIM	GRCh38.p7	X:74613797	ATCCTTCCAGTGATA[A/C]CTGGCAAAGGATATG	51132
rs781617856	snp	G/T	2.30476e-05	0.00339459	missense	RLIM	GRCh38.p7	X:74594351	GGCCTTCTTTAATTT[G/T]CTGTAGTCGTCTCAG	51132
rs781638544	snp	C/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74598553	GGAGGCTGAGGTGGG[C/T]GGATCACGAGGTCAG	51132
rs781735437	snp	A/G	0.0026455	0.0362733	intron-variant	RLIM	GRCh38.p7	X:74608766	AAAACAGTTAAAACT[A/G]AAAGAGTGTTAAGAA	51132
rs781779759	snp	G/T	0.000529661	0.016265	intron-variant	RLIM	GRCh38.p7	X:74607829	GTCAATGAAGAAAAT[G/T]TTAAATACCATCACC	51132
rs786205133	snp	A/G			missense	RLIM	GRCh38.p7	X:74592248	ACAACACTGTCACCT[A/G]TGAAAGTGAACGAGG	51132
rs796174054	snp	A/C			utr-variant-3-prime	RLIM	GRCh38.p7	X:74586521	TCCTTCAGATCTGAT[A/C]AAGACATGAGAATTA	51132
rs796592019	snp	A/G			utr-variant-3-prime	RLIM	GRCh38.p7	X:74583209	GACTCTGGAGACTTG[A/G]GCATATGAAGAAGTT	51132
rs796755702	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74583162	GGTGGGCTTGTAGTA[C/T]AGCTACAGCTTCATC	51132
rs796963298	snp	C/T			utr-variant-3-prime	RLIM	GRCh38.p7	X:74591017	CTGGGAATGATATAG[C/T]TTTAATCACTTATGA	51132

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