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

KLHL12

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs540695210	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902073	ATTACCCATAGTTCC[A/G]CAATACAAAGACACA	59349
rs540702981	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202920502	CTGGCTCAGCCTCCC[A/G]AGTAGTTTGGACTAC	59349
rs540940131	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914633	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	59349
rs541046152	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202909691	TGGCCTATATGAACT[G/T]TGTCAATAGGGCTTC	59349
rs541191609	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896379	ACTTTTTTGTAGAGA[A/C]AGAGTCTCACCATAT	59349
rs541232203	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904081	TGGAGTGCAATGGCA[C/T]GATCTTGGTTCACCA	59349
rs541234397	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202926500	GTGATTCATCAAAGC[A/G]TATGTTTTTCAAAAA	59349
rs541375027	in-del	-/CTTG	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202926194	ATCGATGGACTTACA[-/CTTG]CTTAAGATATTGAAG	59349
rs541418190	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917278	AGAGTGCAGTGGTGC[A/G]ATCATGGCTCACTGC	59349
rs541454944	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202923957	CATACATGTAAGTGT[A/C]AATTATATAATAAAC	59349
rs541455236	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202916383	TTAAGGCCAGGAGCC[A/G]TGGCTCACACTTATA	59349
rs541588353	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202892796	GACCAGCCTGGGCAA[C/T]ATGGTGAGACCCTGT	59349
rs541690152	snp	A/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927914	TAGAACCTGGGAGGC[A/G]GAGGTTGCTGAGCCG	59349
rs541784303	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202906663	ATATATTTTATTTAA[A/T]TAATTTATTTATTTT	59349
rs541862985	snp	C/G	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202905865	GCTGGAGTGCAGTGG[C/G]GTGATCTCAGCTTAC	59349
rs541972072	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900622	TAATCACAGCACTTT[A/G]GGAGGCCGAGGCGGG	59349
rs542030316	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902419	TGGGTAACAGAGCGA[A/G]ACTCCGTCCAAAAAA	59349
rs542051701	in-del	-/TATG	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202903996	ATCTATCTATGTATC[-/TATG]TATCTATCTATCTAT	59349
rs542070288	in-del	-/A			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929509	CTCTATTATTGGTGT[-/A]AAAAGGTGGAAGATA	59349
rs542186358	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202897266	TGGAGACAGAGTTTC[A/G]CTCTTGTTGACCAGG	59349
rs542187499	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907083	TCCTTCAATCTATCT[G/T]GTGTTGATATGTATC	59349
rs542207416	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897926	CAACTATATGATCAC[A/G]TTCCCTGCCAATTCA	59349
rs542351483	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905278	TACCTCCAAAGAATC[G/T]TCTGGGTTTACTGAT	59349
rs542352882	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202909398	TCTATCGCAGCGCTT[A/C]CATTTAACTATTTTT	59349
rs542396777	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901609	ACCAGCCACTCAGGG[A/G]TTTTATGGCTCTAAA	59349
rs542486417	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202904764	GTTAGAGAAATAAGG[C/T]AGATGCAGGACTGCT	59349
rs542578200	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202895402	CTGTCTCAAATAATA[A/G]TAACATTTGACCTTA	59349
rs542581731	snp	C/T	0.00755907	0.0610114	intron-variant	KLHL12	GRCh38.p7	1:202896204	TACAAACTTTTTTTT[C/T]CTGAGTTGGGATCTC	59349
rs542617244	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905768	AAGTTTTAGATCTTG[A/G]AGCATTTTGAATTTC	59349
rs542644663	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202921942	GTCACTAGCACATTA[C/T]TTTGAAAAAACATAT	59349
rs542770974	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914268	GCCAAGAGCTAGAAG[A/G]GGTTAGATGCTGCTC	59349
rs542788645	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908907	AAGAAAAGGTCTGAA[A/G]CGAGGTGTCTGTACT	59349
rs542790596	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202915990	TTATATGTAGTGAAC[A/G]TCAAATCTGTAGTGC	59349
rs542795457	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924063	TGGGATCTTGAAAAA[C/T]AAAGATTTGCAATGT	59349
rs542827774	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202915264	CAAGACTAAATCCCA[C/G]TTGGACTCTAAAACC	59349
rs542864239	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202914564	AGGTTTTTTAGTTTG[C/T]GTTTTTAAGACTAAT	59349
rs543018315	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929825	AGAGCACGCCTCAAA[A/C]TATATTTATATGTTC	59349
rs543132622	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893495	TATAGAAATAAACTA[C/T]GGTCACTAATGACTA	59349
rs543185396	snp	G/T	0.0138799	0.0821421	intron-variant	KLHL12	GRCh38.p7	1:202905949	AGCTTGAACTACAGG[G/T]GCCCGCCACCACACC	59349
rs543187282	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202920219	CTCAGGAGGCTGAGG[C/G]AGGAGAATTGCTTCA	59349
rs543223976	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912393	GCTTCATCCAGCCAA[A/C]GAAGTCGAAGTGGTT	59349
rs543400927	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919551	GCTCTCTTTTATAGA[A/G]CCAAATACTCATATC	59349
rs543428980	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925922	GCAGCCTGGCCAACA[A/T]GGTGAAACCTAGTCT	59349
rs543465728	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202899685	ACAAAAATTAGCCGG[A/G]TGCAGTGATGCGCAC	59349
rs543466200	snp	C/T	1.6636e-05	0.00288405	intron-variant	KLHL12	GRCh38.p7	1:202918164	TAACATCAAGACAAA[C/T]CCGTACCTGAATTTC	59349
rs543502795	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924840	AGTGGTAGATCTTAT[C/T]CAGAATCTGCCAAAA	59349
rs543572478	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202911996	GCTTTGGGTTTGTCA[C/T]ATATGCCATTGTGGA	59349
rs543985182	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202921114	TCCCAGGTTCAAGTG[-/T]TTTCTCGTGCCTCAG	59349
rs543986883	in-del	-/C	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202900223	TAACTCCCTGCCCCA[-/C]CCCCCAACCCCCCAA	59349
rs543999383	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897142	TTTTCCTTGAGGCTG[C/T]AGCTCTCGAGTCTCT	59349
rs544047500	in-del	-/C	0.00318978	0.0398085	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891987	CTCTCTCTCCCTTGT[-/C]CCCAAAGTTTTGTGG	59349
rs544107965	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202893485	GAATCTGAATTATAG[A/T]AATAAACTACGGTCA	59349
rs544121166	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202923502	TGAGCATTGGCTCAT[A/C]GTATTTTTAACTATA	59349
rs544135222	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202926306	CTTTCTGAAATGATC[C/T]GGGGGGAAGGAAATC	59349
rs544175638	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893554	GGAATGGGCCCACAC[A/G]GGCCTAGAATAATCT	59349
rs544203284	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202899475	TTATGTACTTGCCAA[A/T]TAAAGTGGACCCTCT	59349
rs544205579	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914295	GCTCTGGTACATTAG[A/G]CAAAAGGTGACGGTG	59349
rs544238342	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907184	GCCCTATCTAAAAGT[C/T]CTCTTTTTAAAAAAA	59349
rs544246790	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891910	ATTCAGTTTAATTCA[C/T]TTAATTCTAACTTCA	59349
rs544426433	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928215	GGGAGGCGGAGGTTG[C/T]AGTGAGCTGAGATCG	59349
rs544463297	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927356	GTACCCTAGCGCGGG[G/T]CTTCTGTACGCTGCT	59349
rs544515856	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901364	TCGACCTCCCAGGCT[C/T]AAGCAATCCTCCTAC	59349
rs544550803	snp	G/T	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202900681	CCAGCCTGGCCAACA[G/T]GGTGAAACCCCATCT	59349
rs544566755	snp	C/G			missense	KLHL12	GRCh38.p7	1:202911099	GGGGGTTAGTAGGGG[C/G]ATCCGCACATACTGT	59349
rs544726140	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202898884	AAATTACACAAACAC[A/G]TGAGAATAAGGAATT	59349
rs544739430	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202903151	GGAGCCAGAGTGAGA[A/C]CTTGTCTCAAAAAAA	59349
rs544861657	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202924372	TTCACATATTGTTAG[A/G]AGGAGTGGGATGTGG	59349
rs544918073	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892472	CTGGAAAGGATTTTT[G/T]ATTCTCCCACTAACT	59349
rs545057489	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915446	TTCTTTCCAGAAAAA[A/G]AGCAAAGGGCAGTCT	59349
rs545172436	snp	C/T	6.59348e-05	0.00574135	missense	KLHL12	GRCh38.p7	1:202918182	GTACCTGAATTTCGT[C/T]GCACTTGATTAGCTT	59349
rs545259753	in-del	-/TTTTAATATTTTTAA	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202891131	GCATTTGAGACCGTT[-/TTTTAATATTTTTAA]GATTTTTAATATTTT	59349
rs545329656	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914070	AGTGAATGAGGGTGA[C/T]AGAGGAGTAAAATAT	59349
rs545451365	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202897577	CATAATCCTTGAGGT[C/T]TTAAGTGCAGGTGAG	59349
rs545560228	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929918	GAGAGGCCGAGGCGG[G/T]CGGATCACCTGAGGT	59349
rs545566263	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202899584	TAATCCTAGCACTTT[C/G]GGAGGCCAAAGCAGG	59349
rs545595520	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202909529	GTGACAGGAAGAATC[A/G]TATTTTGTCTGAAAT	59349
rs545796021	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202916257	GCTGGAAAATAATTC[C/T]TCTACAGTTGGAACC	59349
rs545833991	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202919684	ATGTTCATGATTAAG[C/T]TTACACTATTAATTT	59349
rs545870756	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202926828	CTAAATTCTAGAGAA[A/G]GAAACGAAGTCCTTC	59349
rs545950367	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907011	CTTCCATCCAGAAGG[C/T]ATACAAATATTTTCC	59349
rs545957383	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907093	TATCTTGTGTTGATA[C/T]GTATCTGTGTATAAA	59349
rs546037935	snp	A/C	0.0023933	0.0345097	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890967	AGTGTAAAGTGGCTA[A/C]CTCTTACCTGTGTCT	59349
rs546091449	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929836	CAAAATATATTTATA[C/T]GTTCAATTTTTTAAA	59349
rs546188537	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905157	ACCTCAAGACTATGA[A/T]GATATATAGATTTAT	59349
rs546271999	in-del	-/AACT	0.00835141	0.0640778	intron-variant	KLHL12	GRCh38.p7	1:202923853	ACACTAAGATGATAG[-/AACT]AACTAAAAAAAAAAC	59349
rs546322357	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911569	CTTCTGGTCTTCTCT[A/G]TAACTTTAAGGAAGG	59349
rs546377255	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924535	GAGGCCAAGGCAGGA[A/G]GATTGCTTGAGCCCA	59349
rs546503694	snp	C/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927353	TCTGTACCCTAGCGC[C/G]GGGCTTCTGTACGCT	59349
rs546556512	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897825	TTCTCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG	59349
rs546619950	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893019	GTCTGGCACAGTGGC[A/G]TGCACCTGTGGTCCC	59349
rs546655967	snp	A/C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927159	GAGTGCGGCGCGGGG[A/C/T]TAGCAGGCGGCTCGG	59349
rs546809295	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202922516	TTTTGAGACAGAGTC[C/T]CGCTCTGTCACCCAG	59349
rs546845877	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922074	CATGTATTCCAGAAA[C/T]TTCTCATTCAATAAA	59349
rs546894369	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202906765	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	59349
rs546978431	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202917878	TGTGAAATGAGTGAA[C/T]GGGTAATAGAGAAGT	59349
rs547090313	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202899797	CACTGCACTCCAGAC[C/T]AGGCAACAGAGTAAG	59349
rs547432940	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202923457	TGGAATGACCTGTCA[C/G]GTTCCTGTTTTCCCT	59349
rs547529621	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908350	TATTTGCTAAGATAA[A/T]AGCTAATACACATAG	59349
rs547582342	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202903758	CTCCCCAATAGCTGG[C/G]ATTACAGGCATGCGT	59349
rs547587877	snp	C/T	1.68966e-05	0.00290655	missense, intron-variant	KLHL12	GRCh38.p7	1:202895714	GTCTCTTACGAGTGA[C/T]GCTCTATGGATTTGG	59349
rs547722160	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202895101	TGAAAGCAAAAAGGA[G/T]TATTTGTCGGCTGGG	59349
rs547749265	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202901963	TCCCTGTTGAAAAGA[A/C]TTGAAAAGTATTTTC	59349
rs547857347	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899138	GCCAACAAGGCAAAA[A/C]CCCGTCTCTACTAAA	59349
rs547864700	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915528	ATTTAAGCTTCTAAA[C/T]AAGGTTAGTTATTTG	59349
rs547891912	snp	A/C	0.0138799	0.0821421	intron-variant	KLHL12	GRCh38.p7	1:202905962	GGTGCCCGCCACCAC[A/C]CCTGGCTTTTTTTTT	59349
rs547996937	in-del	-/A	0.477175	0.104362	intron-variant	KLHL12	GRCh38.p7	1:202914865	AGCGAAACTCCGTCT[-/A]AAAAAAAAAAAAAAA	59349
rs548201594	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202919487	TATGTAAGAAAACAC[A/G]TAATTTCTCCTTCCT	59349
rs548564972	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202926092	CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA	59349
rs548659688	in-del	-/ACC	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202926852	GTCCTTCCTCCTAAT[-/ACC]ACCAGGCATATGGCC	59349
rs548790925	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912165	TAAAGAAGACACTGA[A/T]GAACATCACCTAAGA	59349
rs548825762	snp	A/G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919283	AAAAACCTGGGAATT[A/G/T]TAAGGGAAAACAAAC	59349
rs548897081	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202896663	AGGGCCACTGACATT[G/T]CTAAGGCATAATCTT	59349
rs548954653	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914090	GAGTAAAATATGAAG[A/C]TGGAGAGTTAAGCAA	59349
rs548989151	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913698	CAAGGAAGGCCTCCC[A/G]GAAGAAGCAACAAAT	59349
rs549102745	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893926	GATATTTATTAAGCA[G/T]GTACTACACAGGCAA	59349
rs549171437	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920703	TTTTAATAAAGCAAA[C/T]ATGGCACATTATCTG	59349
rs549181264	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202908071	TATAGAGTAATTCAT[A/G]ACTTATAAAATGTTT	59349
rs549218255	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202907425	TGGTCAACATGGAGA[A/G]ACCCTGTCTCTACCA	59349
rs549223713	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202915653	AACTGAAAACATGAC[A/G]AGCTCATAGTTGAGT	59349
rs549290359	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893158	TACCCAAGTCTTGTC[C/T]CTGTCCAAAAATGAG	59349
rs549384766	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202921175	ACCACTACAACCAGC[C/T]AATTTTTTTTTTTTT	59349
rs549391170	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911266	TCACCATCTCAAAAC[A/G]TAACCACGTTCACTT	59349
rs549533061	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202918438	AGTTGGACAGGTGTG[A/T]TCTAGGATATATTCT	59349
rs549575549	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905412	CTGAACATTAACTCT[A/G]TTGATATAAAGAACT	59349
rs549680298	snp	A/G	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202898132	TGGTCTCAAACTCCC[A/G]GCCTCAAGCGATACT	59349
rs549712381	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904582	TCTGCCAATGATGGA[C/G]TACTTGTTAAGTGAG	59349
rs549807870	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917961	GAATAGTGATTCTTA[A/C]CCACTGGGATCATAT	59349
rs549956946	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897331	ACCTCTGCCTCCTGG[A/G]CTCAAGTGATTCTCC	59349
rs549958064	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917588	AGTTATGATTTGGCT[C/T]CTGCTTCTGTAGATC	59349
rs550206287	snp	C/G			downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890651	ATGCACAATCCATCT[C/G]CCAAAGTTGGTAGGC	59349
rs550208116	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902732	TGGTGGCTCACACCT[C/G]TAACCCTAGCACTTT	59349
rs550247475	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896510	CTTCTGAGCTCAACT[A/G]AACACTGGGTTCAAT	59349
rs550347294	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924455	TTAAAAATTTTTAAA[A/C]TTTAGAAGGAAAAAA	59349
rs550498253	snp	C/T	0.00914312	0.0669923	intron-variant	KLHL12	GRCh38.p7	1:202921216	GTCTTGCTCTGTTGC[C/T]CAGGCTGGAGTGCAG	59349
rs550557194	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927144	CAGCCTGTGGGGATG[A/G]AGTGCGGCGCGGGGC	59349
rs550602828	snp	G/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202899760	GAACTGAGGAAGAGG[G/T]TGCAGTGAGCCGAGA	59349
rs550745807	snp	C/T	0.00398564	0.0444627	intron-variant	KLHL12	GRCh38.p7	1:202906754	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC	59349
rs550883171	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202892836	ATTTAAAGAAAGAAA[A/G]AAAGAAATTAGCCTT	59349
rs551092523	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930231	TACTTTAATGATATT[A/G]CCTAATTCCTGACTG	59349
rs551168110	snp	A/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202902731	ATGGTGGCTCACACC[A/T]GTAACCCTAGCACTT	59349
rs551269636	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202910917	CTTGGGGACTACCCA[C/G]CACCACTCTCACTGG	59349
rs551568606	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202908948	TATTATTTTCAACTA[C/T]GTTGTCACCTGCAAG	59349
rs551574535	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202909938	TTCTTTATTAAAAAA[A/T]ACTCTTCTAAAATTG	59349
rs551608686	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202916584	AGAAGGTGAAGGTTA[C/G]AGTGAGCTGAGATCA	59349
rs551651531	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912496	TGGCAGTGAGGATGG[C/T]GATAATGGATTTGGT	59349
rs551663229	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915377	ACTGGGAGTCAGACA[C/T]CTGGTTCCTATTTCT	59349
rs551694751	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202894075	GAGACAAGGAGGAGA[A/G]CAGAATCTCATTTTT	59349
rs551702055	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901065	AAAATAAAGAAAAAA[A/C]CCCTCTCTTTCTTGA	59349
rs551774449	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202914634	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	59349
rs551875969	in-del	-/T	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202917916	AGATACCTACTTTAC[-/T]TCCAATTTCTGCTTA	59349
rs551905759	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912095	CTGTTTCAAGGGAAG[A/G]TTCTCAAAGACCAGG	59349
rs551920505	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202894926	AAAAAGAATGGGGTA[A/G]AACAAAATCCTTAAA	59349
rs551925047	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891267	CACTCCTAATACCCA[C/T]AAAACAAGAATTTCA	59349
rs551963778	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898972	TCTTTTAGAGACACA[C/T]GTGGAAGTATGACAC	59349
rs551963884	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890696	ATAACTTCCTCATGT[A/G]GCTCCTCCTTCCTTT	59349
rs552249255	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902671	AGAAATGGGAAGAAT[A/G]CTGAGTAATGAACCT	59349
rs552393654	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202922402	GAAACCCCGTCTCCA[C/T]TAAAAATACAAAAAA	59349
rs552424872	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202921125	AAGTGTTTCTCGTGC[C/T]TCAGCCTCCCAAGTA	59349
rs552563608	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917929	ACTTCCAATTTCTGC[C/T]TATTCTATACTCTGT	59349
rs552745782	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202922766	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	59349
rs552770055	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927273	ATGACGCAATGCAGC[C/T]GGAGCACCGCCCTCC	59349
rs552777463	snp	A/G			missense, intron-variant	KLHL12	GRCh38.p7	1:202896876	AAGCTCCACTCCTGA[A/G]TCTTGGGGTCATATT	59349
rs552834244	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925340	GTTGAGGGCACTCCT[A/T]TGCCTGGCATCACCA	59349
rs552917222	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907061	CTCATAGTTTTTCAC[C/T]ATTCAGTCCTTCAAT	59349
rs553055521	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202918886	TCACACTGTTTAAAT[C/T]ATGTATTAAAAACTA	59349
rs553086687	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202905823	AACCCGATTTTTTTT[A/T]AGACAGAGTCTCACT	59349
rs553120717	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907814	TTGGGAGGCTGAGGT[A/G]GGAAGACTGCTTGAG	59349
rs553121931	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912292	ACCATGACTCTGTGA[A/G]TAAGACTGCCATTCA	59349
rs553144568	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892418	ATCACTGCACTGGTG[C/G]CTGTAATCACCCGGT	59349
rs553230504	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914167	CAACTTGAAATCATC[C/T]GAAGGTTTCAAGCAG	59349
rs553267400	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202913826	CCAATACACTACCCA[C/T]GCGTGGCTATTTACA	59349
rs553269230	snp	G/T	0.0023933	0.0345097	intron-variant	KLHL12	GRCh38.p7	1:202921367	TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC	59349
rs553381270	snp	C/T			intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927163	GCGGCGCGGGGCTAG[C/T]AGGCGGCTCGGGAGG	59349
rs553452152	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915155	GGCGTTCTTATTTTA[C/T]GCTCAGAACAGTCCT	59349
rs553476035	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202910093	AAATAGTAGTAAACA[C/T]TTATGTACAAAGACT	59349
rs553579615	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891734	TACTGAACTCCCACA[C/T]TGATGTCATCTTCTC	59349
rs553618309	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202899416	TTAATAAAACATATA[A/C]ACTCACACATAAACC	59349
rs553654149	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898688	GAAATTCTACAGGTC[A/G]AACAGCTTGGCTTCT	59349
rs553717247	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202902340	GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACTTG	59349
rs553724866	snp	A/C	0.000399281	0.0141238	missense	KLHL12	GRCh38.p7	1:202894268	AATTTAAGATATTCA[A/C]GCCGTCATATCCTCC	59349
rs553763426	snp	A/G	1.64833e-05	0.00287078	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202893313	GGTCATACTGGTGAC[A/G]GTTGTCCAGGAATCA	59349
rs553895398	in-del	-/AGCCACTGTACC			intron-variant	KLHL12	GRCh38.p7	1:202901585	GGGATTACAGACATG[-/AGCCACTGTACC]AGCCACTCAGGGGTT	59349
rs553897387	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202901145	AGGAAATAGATTATA[C/T]TAAAAACACAGATAA	59349
rs553984285	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922291	AGATAAAGGGGGGCC[A/G]GGCACATGGCTCAAG	59349
rs554028126	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896101	ATTTATTATAAGAAC[C/G]TTAAAAGGTAGGAGG	59349
rs554064319	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202895288	GTCCCAGCTACTCAG[A/G]AAGCTGAGGTGGGAG	59349
rs554124828	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890837	CCTGAAATTCAAGCG[C/T]GTGCTAAGTGAATTC	59349
rs554339641	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912332	TCCTACGAATGGCCA[C/T]AACTGTGAAGTTAGG	59349
rs554529231	snp	A/C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920040	AATTACAGGCCAGGC[A/C/G]TGGTGGCTCATGCCT	59349
rs554541275	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202926597	TGAAGACAGCCCGGG[A/G]GGTCTTTTATCGTTT	59349
rs554566761	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898508	TTGAGTGCTTCCTAA[C/T]GGTGATGAATAGGAA	59349
rs554748547	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202920184	TTGGGCATGGTGGCA[C/G]ATGCCTGTAGTCCCA	59349
rs554785502	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927203	GCCGCCCAGACCCGG[A/C]GGCTCTGGAGGCTCT	59349
rs554853621	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904976	TCCTTCTGCTGTATG[C/G]AGAAGAGTCATTATC	59349
rs554964809	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926857	TCCTCCTAATACCAC[C/T]AGGCATATGGCCGCC	59349
rs554980678	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892110	AAGACTTGGATTTTA[C/T]CAAGTTTACTTAAAC	59349
rs555022922	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202923982	ATAAACAGTGATGCA[A/C]CCACAACTGAGCTTT	59349
rs555143477	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920938	AGAAATTTCATGTTC[C/G]TAGAGGAGCCTGTGG	59349
rs555172853	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904165	ATGTGCCACCAAGCC[C/T]GGCTAATTTTGTATT	59349
rs555180355	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928119	CTCCACTAAAAATAC[A/C]AAAAAATTGGCTGGG	59349
rs555228770	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911773	GCCTGTGGACGCCGC[C/T]GAAGAAGCATCTTTA	59349
rs555292403	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900634	TTTGGGAGGCCGAGG[C/T]GGGTGGATCACTTGA	59349
rs555331769	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202906865	TGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	59349
rs555460017	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899438	ACATAAACCACGGAG[C/T]TTTTCTAAGAGGGCA	59349
rs555523941	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901225	ACTATATGTCTACAG[C/T]GGAACTTCGTAAGAG	59349
rs555622641	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908524	TTAATAAATCTAGTA[C/T]GAGGTAAACTGGTAC	59349
rs555661469	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907907	AGTGAGACCTCATTT[A/C]TATTAAAAAAAATAA	59349
rs555764698	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202903124	AAGATCATGCCACTG[C/T]ACTCTAGCCTAGGAG	59349
rs555792200	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202910297	CAGAGTCTGTGCTCC[C/T]AAACACAATGTAAAG	59349
rs555831696	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891873	AATACTTCAGTGCTG[A/T]TCTAGGTTCACTCAC	59349
rs556064563	in-del	-/AGAG	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202922865	TTCAGGAAAAAAAAA[-/AGAG]AGAGAGAGAGAGACA	59349
rs556130756	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900997	GTTGCAGTGAGCCGA[A/G]ATCATGCCGCTACAC	59349
rs556229646	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896890	AGTCTTGGGGTCATA[C/T]TTCTCTACCACATCA	59349
rs556271132	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914085	TAGAGGAGTAAAATA[C/T]GAAGCTGGAGAGTTA	59349
rs556334182	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202909446	TTCCAGGGATTATGC[A/C]AACACAAGTACATAA	59349
rs556478188	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202916875	GCTACACAGGAGGAT[C/G]AGGTGGGAGAGCTGC	59349
rs556514735	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202923756	TATGCACAACAATTA[C/G]TAGCACAGTACCTGG	59349
rs556787308	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922788	ACCACGCCCAGCTGA[A/C]GATCCAAGACTTAAC	59349
rs556887587	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930598	AGTTATTTTAAAATG[C/T]ACAATTCAATTATTA	59349
rs556910589	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913063	CTGAATAAATGTCTT[A/T]AAAAAAAAACAAGAA	59349
rs556975601	snp	C/T			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927457	GCAGGCCGAGGCGAG[C/T]GAATTACCTGAGCTC	59349
rs557038614	snp	G/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202926738	CTATTTTCTAGAACT[G/T]TCGTTAACATCTGAA	59349
rs557155137	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202918868	TGCACTAATGCAAAA[A/G]CTTCACACTGTTTAA	59349
rs557300053	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927225	GGAGGCTCTGGAGCC[A/G]TCCGGGTCTGGCCCC	59349
rs557386205	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911831	CTAAGTCAGAGTCTC[C/T]TAAAGAGCCCAAACA	59349
rs557388684	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909847	AGGCTTAGGGGTTGT[C/T]AATAGCTTATGTCCT	59349
rs557425008	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929615	GAACTGTTTGGTTGT[A/G]AGACAGGGTGGGAAG	59349
rs557436898	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202921707	GTTTAGCTAAGAGAA[C/G]AAATCTTCAATTTTA	59349
rs557463978	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915861	AGTGGACAGGGATTT[G/T]TGTTTTGTTCATAAT	59349
rs557501619	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202898362	TAACCTGGACTTGAA[A/G]GAGCAAATGTAGTAC	59349
rs557576981	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898610	CTAGTTTACAGGCAA[C/T]ACATGGGAGAAGAAC	59349
rs557590643	snp	A/C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912196	GATAATTTGAACAGT[A/C/T]TGGAAAAACGGAAGT	59349
rs557590880	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202906755	CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT	59349
rs557607639	snp	C/T	0.00478085	0.0486577	intron-variant	KLHL12	GRCh38.p7	1:202905684	AACTATTTGCGCATC[C/T]CTAATTCAGAAACCC	59349
rs557727117	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202908598	ACTGGGCTCCTTTTC[C/T]TCCTCTCTTCATTCC	59349
rs557749409	snp	A/G	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202907499	CCCAGCTACTCGGGA[A/G]TCTGAGGCACAAGAA	59349
rs557753328	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899866	AAATAAAAAAATCAA[A/G]GCATAAGAATGAAGG	59349
rs557764307	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915100	ATAGATTTTCTCCAC[A/T]ATACATTTTCACAAA	59349
rs557818049	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930588	GTATACTTTTAGTTA[C/T]TTTAAAATGTACAAT	59349
rs557829064	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202911410	TAGTCAATTTGGGTT[-/A]AAAAAAAAAATATAT	59349
rs557843302	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202907265	CTTCTCTGTATTTCT[A/G]CAAGTTCTACATTGA	59349
rs557888228	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928871	CTCTTGCTCTGTCGC[C/G]GAGGCTCGAGTGCAC	59349
rs557960444	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202910053	CAAGAAGTTCTTAGT[C/T]GAACTGGAAAGGAAA	59349
rs558037510	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901392	TACCTCCCAGGCTCA[A/G]GCAATCCTCCTACCT	59349
rs558107582	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897420	TGTATTTTTAGTAGA[C/G]ATGGGGTTGGTCAGG	59349
rs558343647	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202901673	TTCTTTGCTGTGAAG[C/G]ACTCTCTTCATTATT	59349
rs558360725	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202922501	AAGACTTTTTTTTTT[C/T]TTTGAGACAGAGTCT	59349
rs558371009	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925800	TCCAAACATATCTGG[A/C]TTTCTTCTTAAAATG	59349
rs558538889	snp	A/C	0.00517822	0.0506191	intron-variant	KLHL12	GRCh38.p7	1:202904770	GAAATAAGGCAGATG[A/C]AGGACTGCTAAAATA	59349
rs558562529	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892302	AATGTGGTCTCTCAC[A/G]TCCATTCAATGTGCA	59349
rs558631959	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202914285	GTTAGATGCTGCTCT[G/T]GTACATTAGGCAAAA	59349
rs558817679	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202896403	ACCATATTGCCCAGG[A/C]TGGTCTTGAACTCCT	59349
rs558875196	snp	A/T	0.00398564	0.0444627	intron-variant	KLHL12	GRCh38.p7	1:202911417	ATTTGGGTTAAAAAA[A/T]AAATATATATATATA	59349
rs558909667	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202918445	CAGGTGTGATCTAGG[A/C]TATATTCTTGTATCT	59349
rs558915601	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202917977	CCACTGGGATCATAT[A/G]TCTAATTGAAGAAAG	59349
rs559054871	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202916274	CTACAGTTGGAACCA[A/G]TGTGACCAATGTGCT	59349
rs559115326	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892059	CCCTAGCTACCTGTA[G/T]ATGAGAAAATGTAGT	59349
rs559125491	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912442	TCGTGGAGGTGGTTT[C/T]GGTTGGCATGACAGC	59349
rs559137185	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202910454	TTGTAGTTAACTAAG[A/G]GATCTAGGGCTGGGC	59349
rs559151960	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899604	GCCAAAGCAGGTAAA[C/T]TGTCTGAGGTCAGGA	59349
rs559170364	snp	C/G	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202917228	TATTCCTTCTTCCCC[C/G]GCAAGAGACAGGGTC	59349
rs559261851	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924668	AGAAATAGTAAAATC[C/T]AATAGCTGACATGTG	59349
rs559312215	snp	C/T			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927806	CCAACATGGTGAAAC[C/T]CTATCTCTACTGAAA	59349
rs559347686	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202920521	AGTTTGGACTACAGG[A/C]GCCCGCCACCACGCC	59349
rs559390540	snp	A/C	0.0138799	0.0821421	intron-variant	KLHL12	GRCh38.p7	1:202905957	CTACAGGTGCCCGCC[A/C]CCACACCTGGCTTTT	59349
rs559430202	snp	G/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202920354	AAAAAATAAAATTAT[G/T]CTCTATTTTGTTGGA	59349
rs559466552	snp	A/T	0	0	intron-variant	KLHL12	GRCh38.p7	1:202919687	TTCATGATTAAGTTT[A/T]CACTATTAATTTTCA	59349
rs559597037	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924575	GACCAGCGTGGGCAA[C/T]ATAGTGAGACCCTGT	59349
rs559599559	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202913137	ACGCACTATGCTATT[A/T]GAGAAGATATATTTA	59349
rs559743261	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928031	ACGCCTGTAATCCCA[G/T]CACTTTGGGAGGCCG	59349
rs559765383	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911925	CTATTTTGAGCAATG[C/G]GGAATGCTCACGGAC	59349
rs559770871	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202897830	CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	59349
rs559865382	snp	C/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929880	CTGGGCACAGTGGCT[C/G]ACGCCTGTAATCCTA	59349
rs559883940	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202926534	TTAAGTCAACTTAGT[G/T]GCAACTCTAGGGGTG	59349
rs559919651	snp	A/G	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202901554	CGATGCTTCTGCTTC[A/G]GCCTCCCAAAGTGCT	59349
rs560001637	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890977	GGCTACCTCTTACCT[A/G]TGTCTAACATAGAAA	59349
rs560036577	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202899142	ACAAGGCAAAACCCC[A/G]TCTCTACTAAAAATA	59349
rs560048666	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902302	AGACATGGTAGCACA[C/T]GCCTGTAATCTCAGC	59349
rs560196474	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908029	TCAGATAAAAGGAAA[A/C]AATAAAACAAAATAC	59349
rs560220069	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893873	TGAAGGTAAGTAGCT[A/T]CTCTTTTGTCCTTAT	59349
rs560353335	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914470	AAATAGTTTTAAGCA[C/G]ATACATGATAGACTC	59349
rs560429352	in-del	-/G			intron-variant	KLHL12	GRCh38.p7	1:202911771	CTGCCTGTGGACGCC[-/G]CCGAAGAAGCATCTT	59349
rs560583757	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928350	GGGTCCGGCAGGGAG[C/G]CTGGGAATGTATCTA	59349
rs560645082	in-del	-/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202901938	CCATCCCCACTCACG[-/T]TATTACCCCTCCCTG	59349
rs560769620	snp	C/T	7.89578e-05	0.00628273	intron-variant	KLHL12	GRCh38.p7	1:202925231	GGGAAAAAAAAACAA[C/T]GAGCATATTCAAAGA	59349
rs560785370	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911963	TAATGAGAGACCCAA[A/C]CACCAAGTGCTCCAG	59349
rs560821155	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202918986	CCAGGAACGGTGGCT[C/T]GTGCCTATAATTCCA	59349
rs560859667	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	KLHL12	GRCh38.p7	1:202918303	CAGGTCAACACAATT[A/G]TGGGTTTCAGCAAAA	59349
rs560886645	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202911778	TGGACGCCGCCGAAG[A/G]AGCATCTTTAAAGTC	59349
rs561180743	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917964	TAGTGATTCTTACCC[A/T]CTGGGATCATATATC	59349
rs561245809	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202925875	CTTTAGGAGGCTGAG[A/G]TGGGTGATCAGTTGA	59349
rs561301168	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202909701	GAACTGTGTCAATAG[C/G]GCTTCCTATGCCTTC	59349
rs561343850	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896457	CAGCCTCCCAAAGGG[C/G]TGGGATTATAGGTGT	59349
rs561699118	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202906707	CACTCTGTCGCCCAG[A/G]CTGGAGTACAATGGT	59349
rs561939116	snp	A/C	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202892806	GGCAACATGGTGAGA[A/C]CCTGTCTCAATAAAA	59349
rs561975151	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900119	ATGTATGAATAAAAA[C/T]TCCCACACCAACCAA	59349
rs561989791	in-del	-/A	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202907911	GACCTCATTTCTATT[-/A]AAAAAAAATAAAATA	59349
rs562101014	snp	C/T	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202906040	TAGCCTGGATGGTCT[C/T]GATCTCCTGACCTCG	59349
rs562133886	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898858	ACAAACAACAAAAAA[C/T]TATGGAAAAAAAATT	59349
rs562172214	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905883	GATCTCAGCTTACTG[C/T]AGGCTCCATCTCCTG	59349
rs562201097	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902417	CCTGGGTAACAGAGC[A/G]AGACTCCGTCCAAAA	59349
rs562228567	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202927016	GGAGACCAAGGATGG[A/G]GGGTAGGGCCATAAC	59349
rs562354279	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927327	GTGAGGAGGTGGTGT[C/T]ACGTGACCTGTCTGT	59349
rs562369125	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202895427	ACCTTAATTTTTTCT[C/T]CGTATTTCATGCTCC	59349
rs562566041	snp	A/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202894863	GCAAAAACAAAGTAT[A/T]TTTAAATGAGATAAG	59349
rs562656502	snp	A/G	8.24083e-05	0.00641852	synonymous-codon	KLHL12	GRCh38.p7	1:202911153	CCGCTCTTTCTTGGC[A/G]TGCTTCACCCAGTTG	59349
rs562737659	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202901637	AAATGGCTGGGATCC[C/T]TCGATCACTGATTCC	59349
rs562757079	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202908363	AATAGCTAATACACA[C/T]AGTTATTATGTGCCA	59349
rs562773357	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908908	AGAAAAGGTCTGAAA[C/T]GAGGTGTCTGTACTT	59349
rs562783253	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202923165	GTTTTTAAAGAAAGA[A/C]ATCATCACTGATGAG	59349
rs563048767	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922371	AGGATATCGAGACCA[C/T]CCTGGCTAACATGGT	59349
rs563139853	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898906	TAAGGAATTGTGTGA[C/T]TTTAAACAGTGATAA	59349
rs563176698	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905950	GCTTGAACTACAGGT[A/G]CCCGCCACCACACCT	59349
rs563353806	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925939	GTGAAACCTAGTCTC[C/T]ACTAAAAATACAAAA	59349
rs563383771	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202926895	GGTGGAGGTATCGGA[A/G]AGGGGCAGTTCAGGG	59349
rs563390506	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925315	CTTCCTCAGACCCAA[A/G]CATACACAAGTTGAG	59349
rs563439812	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912016	GCCATTGTGGAGGAG[A/G]TGGATGCAGCCATGA	59349
rs563565559	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912397	CATCCAGCCAAAGAA[A/G]TCGAAGTGGTTCTGG	59349
rs563604446	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919665	TCCATAGTTTGTCTC[C/T]AAAATGTTCATGATT	59349
rs563637684	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917578	CTCACAAGACAGTTA[C/T]GATTTGGCTCCTGCT	59349
rs563668342	snp	A/C	0.00478085	0.0486577	intron-variant	KLHL12	GRCh38.p7	1:202904192	TATTTTTAGTAGAGA[A/C]AGGATTTCTCCATGT	59349
rs563699675	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896515	GAGCTCAACTGAACA[C/T]TGGGTTCAATTCAAC	59349
rs563706928	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202903533	GGTGCAATTATGGTT[C/T]ACTGCAGCCTCAGCC	59349
rs563707044	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911506	TACCTAATAAATCAC[C/T]AGTCACGTATTGGCC	59349
rs563743878	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202910883	ACTTGCCAAGAAATT[C/T]GCTTTTCTTAGAAAT	59349
rs563775912	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904895	CTTTGAGACAGTAAT[A/G]GGTAAGGTTAATAAC	59349
rs563790221	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897150	GAGGCTGTAGCTCTC[G/T]AGTCTCTGAAACTTA	59349
rs563915705	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202892849	AAGAAAGAAATTAGC[A/C]TTCTATTCCTTTCCA	59349
rs563991411	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914349	GTGGTGAGCCACTGG[A/G]GAAATACTTGGGAAG	59349
rs563993670	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202923899	AAAAACTTGTGCTTA[A/G]AAAGACTTTTAAAAC	59349
rs564061945	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202900777	GGTGAGGCACGAGAA[A/T]CGCTTGAACCTGGGA	59349
rs564097105	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900166	TATGCAAATTTTAAA[C/G]TTTTCTATTGATTTT	59349
rs564116928	snp	C/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929078	TCGTGATCCGCCCGC[C/G]TTGGCCTCCTAAAGT	59349
rs564178392	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902909	AGGCTGAGGTGGGAG[A/G]ATCACTTGAGTCCAG	59349
rs564211502	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913937	GCTAGCGGGAGCAAA[C/T]CAGACACTATAGATA	59349
rs564385188	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	KLHL12, RABIF	GRCh38.p7	1:202891115	TTAGCCACAAACTCT[C/T]GGCATTTGAGACCGT	59349
rs564418938	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928254	TACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC	59349
rs564528006	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891927	TAATTCTAACTTCAA[C/T]TCTGATATACAAATC	59349
rs564593442	snp	A/G			synonymous-codon	KLHL12	GRCh38.p7	1:202918300	CATCAGGTCAACACA[A/G]TTGTGGGTTTCAGCA	59349
rs564602986	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202920525	TGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC	59349
rs564643062	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202900374	CATGGTGAGACTCCC[A/G]TATCTAGAAAAAAAT	59349
rs564750439	in-del	-/TTTAACCC	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202903959	TTACACACAAATGGT[-/TTTAACCC]TTTAACCCTTTATCT	59349
rs564815058	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	KLHL12	GRCh38.p7	1:202925085	GGTATTGCTCTTCCT[A/G]AGGGAGTTCATTGAA	59349
rs564851439	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924398	TGTGGTTTGAATCCT[A/T]CTCCTCTCTCCTTCC	59349
rs565126116	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202895469	AGGAGAGGTTAAAAA[C/G]CCTGGTCCAGCCACA	59349
rs565363072	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929973	AACGTGGCAAAACCC[C/T]GTCACTACTAAAAAT	59349
rs565408561	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202909570	AGGTTCACAGTCCTG[C/T]TGTAATTACCATTGT	59349
rs565442620	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202916124	ATGCCTGCCACTTCA[A/G]CACAAGGATACAATG	59349
rs565534035	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893546	AGGGATATGGAATGG[A/G]CCCACACGGGCCTAG	59349
rs565567974	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891328	GCTCAGAAATGTTGA[C/T]AGCTGAGGTACTGAA	59349
rs565595849	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202897732	GTGATGGATTTAAAA[A/T]CTCTTTTTCTTTTTC	59349
rs565604851	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890755	TTTTGCAGGCCTTCC[A/G]CATAGCTGTTTATAT	59349
rs565605152	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898973	CTTTTAGAGACACAC[A/G]TGGAAGTATGACACA	59349
rs565617534	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904873	AAAGTAATTTCCATT[A/G]TATCTTCTTTGAGAC	59349
rs565641219	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898408	AAACACAGATAAACC[C/T]CTAATGAAGTAATGG	59349
rs565649670	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911770	TCTGCCTGTGGACGC[C/T]GCCGAAGAAGCATCT	59349
rs565745803	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912158	GCAGCATTAAAGAAG[A/G]CACTGAAGAACATCA	59349
rs565929019	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202919690	ATGATTAAGTTTACA[A/C]TATTAATTTTCAACC	59349
rs565930511	in-del	-/AA			intron-variant	KLHL12	GRCh38.p7	1:202907612	TAAAAAAAAAAAAAA[-/AA]GGAAAAAAATTATAT	59349
rs566027420	in-del	-/TATC			intron-variant	KLHL12	GRCh38.p7	1:202903992	ATCTATCTATCTATG[-/TATC]TATCTATCTATCTAT	59349
rs566183122	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202896031	CTGGGCTAAGAGACT[A/G]ATATCCTTCCATAAA	59349
rs566258702	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202894578	TCCCATTCCTGCATC[C/T]CAGACTCAATACCTA	59349
rs566401401	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202924670	AAATAGTAAAATCCA[A/C]TAGCTGACATGTGTG	59349
rs566532147	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893022	TGGCACAGTGGCGTG[A/C]ACCTGTGGTCCCAGC	59349
rs566577155	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920577	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	59349
rs566614020	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920109	ACCTGAGGTCAGGAA[C/T]TCAAGACCAGCCTGG	59349
rs566756893	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202922087	AATTTCTCATTCAAT[A/G]AACTACATTTCCATC	59349
rs566795540	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202921375	AGATGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG	59349
rs566797048	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915511	TTCTCAAGCTGTTTT[C/T]CATTTAAGCTTCTAA	59349
rs566949246	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202900341	TTGCGCCCAGGGGTT[C/T]GAGGCCACTTTGGGT	59349
rs566972127	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202917879	GTGAAATGAGTGAAC[A/G]GGTAATAGAGAAGTG	59349
rs566987862	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907292	TTGAACATGCAGTAC[G/T]TATGCCATTAAAAAA	59349
rs567005990	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202916838	TTAAAAAATTAGCCC[A/G]GTGTGGTGATGTGCA	59349
rs567065072	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892419	TCACTGCACTGGTGC[C/T]TGTAATCACCCGGTG	59349
rs567125273	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202906792	TCAGCCTCCAGAGTA[G/T]CTGGGATTACAGGTG	59349
rs567158391	in-del	-/CT			intron-variant	KLHL12	GRCh38.p7	1:202909773	CTCTCAAGGCAGTGA[-/CT]CTACACGATTCTCTT	59349
rs567249928	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906688	TATTTTTGAGATGGA[A/G]TCTCACTCTGTCGCC	59349
rs567324030	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202912260	GAAAAGGGGCTTTGC[C/T]TTTGTAACCTTTGAT	59349
rs567450404	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897305	CAATTCCATGATCTC[A/G]GCTCACCACAACCTC	59349
rs567589931	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202901996	TGTGATTATAAAACA[C/T]ATAATATACATTTTT	59349
rs567628169	snp	A/G	1.64982e-05	0.00287208	missense	KLHL12	GRCh38.p7	1:202909115	ATTGTAAACTACAGC[A/G]GATGAAAGGCTGAAA	59349
rs567723778	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901187	TCCTGTTGGCTGAAA[C/T]TTTCCCAATAAACAC	59349
rs567762139	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202908448	TACAGGCAGGTGCTA[C/T]GATGATTCCATTTAC	59349
rs567769716	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915578	TTTTATTCCAAAGCC[G/T]GTATAGTTCCAAAAG	59349
rs567857025	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202918978	ACTGGGGACCAGGAA[C/T]GGTGGCTCGTGCCTA	59349
rs568036296	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202898593	AGCCTCTAATCCAAC[C/T]ACTAGTTTACAGGCA	59349
rs568047261	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891519	TGGGGCAGTAATCAG[A/G]TAGCTGAACTACTAG	59349
rs568168182	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905673	TTTCTTTGCACAACT[A/C]TTTGCGCATCCCTAA	59349
rs568204330	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927773	TTACTTGAGGTCAGG[A/G]GTTCGAGACCAGCCT	59349
rs568222149	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892173	GCCCATATCTAGTAG[C/G]CTATACTCACCTTAG	59349
rs568234375	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903074	GCTGAGGTGGGAGGA[C/T]TGCTTGAGCCCAGAA	59349
rs568240120	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927361	CTAGCGCGGGGCTTC[C/T]GTACGCTGCTAGGAA	59349
rs568257240	snp	C/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927208	CCAGACCCGGAGGCT[C/G]TGGAGGCTCTGGAGC	59349
rs568392113	in-del	-/T	0.291493	0.246533	intron-variant	KLHL12	GRCh38.p7	1:202921178	ACTACAACCAGCTAA[-/T]TTTTTTTTTTTTTTT	59349
rs568557391	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930205	TTCCTTGTTTTCAGG[A/T]TGTAAAATAGTACTT	59349
rs568789703	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922129	ATATGGAAACAATTT[C/T]ACTATGTAAGAACTT	59349
rs568992510	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913719	AGCAACAAATTGAAA[C/T]CTGATGGATGAGTAG	59349
rs569015098	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202903992	TATCTATCTATCTAT[C/G]TATCTATCTATCTAT	59349
rs569038071	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915662	CATGACGAGCTCATA[A/G]TTGAGTGATTAAGAG	59349
rs569114956	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202909289	GCTCTCGGTTTCCAG[A/G]AATGATTTTTAAAAT	59349
rs569216953	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907466	AATTAGCCAGGGATG[A/G]TGGCAGTCGCCTGTT	59349
rs569234809	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202921199	TTTTTTTTTTTGACA[A/C]AGTCTTGCTCTGTTG	59349
rs569350216	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893931	TTATTAAGCATGTAC[C/T]ACACAGGCAAAATTG	59349
rs569353267	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202920736	GCTTTCCAAATGAAG[C/T]AGGTAGTTATCTATA	59349
rs569353755	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202903851	TGGTCTCGAATTCCT[A/G]GGCTCCATCGCCTGC	59349
rs569386455	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202901005	GAGCCGAGATCATGC[C/T]GCTACACTCCAGCCT	59349
rs569392896	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911387	GCTAACAGACCAGGA[A/G]AAGAATTATAGTCAA	59349
rs569506877	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202900378	GTGAGACTCCCATAT[C/T]TAGAAAAAAATAATA	59349
rs569578089	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897338	CCTCCTGGGCTCAAG[G/T]GATTCTCCTGCCTCA	59349
rs569581488	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202904951	TTTTAACTTGGCTGT[C/T]AATTTAATTTCCTTC	59349
rs569619188	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904745	GTGTGTGCTGTGACA[C/T]GTTGTTAGAGAAATA	59349
rs569642674	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202907420	CAGCCTGGTCAACAT[C/G]GAGAAACCCTGTCTC	59349
rs569674182	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911689	CTCAAACTGTTCACC[C/T]AAGCCTCTGAAGCAG	59349
rs569789933	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202920655	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC	59349
rs569822536	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890639	GGTTTAATTAGCATG[C/T]ACAATCCATCTGCCA	59349
rs570065414	snp	C/G	5.00204e-05	0.00500077	intron-variant	KLHL12	GRCh38.p7	1:202919939	GTATAAAAGAATGAT[C/G]GTTATAATTCCACAA	59349
rs570067656	in-del	-/CA	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202919084	GAGAGAACTCATCTC[-/CA]CACAAAAAAATTTTG	59349
rs570136869	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902773	AGCAGGCAGATCACA[C/T]GAACCCAGGAGATCA	59349
rs570166241	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902152	AAACACAAATGGGGG[A/C]CGGGCACAGTGGCTA	59349
rs570315783	snp	A/C/T			missense	KLHL12	GRCh38.p7	1:202925153	CTTTGGGGGCCATAA[A/C/T]GCCTCCCATAAAGCA	59349
rs570319563	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202923762	CAACAATTACTAGCA[C/G]AGTACCTGGCCCATA	59349
rs570380120	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202896429	CTCCTGGCCTCAAGA[C/G]ATCCTCCCATCTCAG	59349
rs570526325	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899768	GAAGAGGTTGCAGTG[A/G]GCCGAGATTGCACCA	59349
rs570602915	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202926283	AGAATCGATATTGGA[A/T]TCCAAAACTTTCTGA	59349
rs570708802	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919386	AATACTACCACTTAA[C/T]GGCCAGATAGATAAA	59349
rs570713829	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202925815	ATTTCTTCTTAAAAT[A/G]AAACTTCAGGCCGGG	59349
rs570747235	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920822	TAACTTTAAAAATCT[A/G]TTTCATATTAAAATA	59349
rs570947079	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202922648	CCCGCCACCACGCAC[A/G]GCTAATTTTTTGTAT	59349
rs570998262	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202922647	GCCCGCCACCACGCA[C/T]GGCTAATTTTTTGTA	59349
rs571071312	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912206	ACAGTTTGGAAAAAC[A/G]GAAGTGATTGAAATC	59349
rs571105734	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912597	ATTTTGGACCCATGA[A/C]GGGAGGAAACTTTGG	59349
rs571141478	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919999	TTAGAGATGTTAATA[A/G]TATTAATTGAACATT	59349
rs571205784	in-del	-/A	0.00318978	0.0398085	intron-variant	KLHL12	GRCh38.p7	1:202893107	TAAAAAAAATCTAAT[-/A]AAAAAAATCAAGTTG	59349
rs571220335	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202916661	TATATTACACAAATA[A/T]CCTAGTTTTAACAAA	59349
rs571429584	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202910017	CAGCTCTAATTAAAT[C/G]GCACCTCTATTAACC	59349
rs571532475	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202894942	AACAAAATCCTTAAA[A/C]GCATTCAAAGACCAC	59349
rs571545319	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929650	TTTTTGCTCTTTGTA[A/T]TTTATTTTGCCTTTT	59349
rs571576432	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202894107	CATTAATCTACGGTT[C/T]GTCCCATGCACCACC	59349
rs571627505	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202914638	TTTGGGAGGCCGAGG[C/T]GGGTGGATCACGAGG	59349
rs571727491	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202914158	CTCTCAGAGCAACTT[A/G]AAATCATCCGAAGGT	59349
rs571749639	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897444	GGTCAGGCTGGTCCC[A/G]AACTCCCAACCTCAA	59349
rs571845482	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202921235	GCTGGAGTGCAGTGG[C/T]GTAATCTTGGCTCAC	59349
rs571853745	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890934	TCAGGTAAATATTTT[A/G]CTGATGAGAATCTCC	59349
rs572043272	snp	A/C/G	3.29464e-05	0.00405861	missense	KLHL12	GRCh38.p7	1:202925089	TTGCTCTTCCTGAGG[A/C/G]AGTTCATTGAATTGA	59349
rs572336944	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202917740	ACATTTTTTTTGTCT[A/G]TATCTCTGTCTCTAC	59349
rs572532606	in-del	-/A	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202904519	CAATCTGACTCGTGT[-/A]AAAAAAAAGCTAGTG	59349
rs572569999	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202923020	CCCAGTGAAGTTAGA[C/T]GGTTCCCAGGGTTTA	59349
rs572598172	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202903351	TTATAACTAATAAGA[A/C]CCTATTATTAATTAG	59349
rs572635664	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202910458	AGTTAACTAAGAGAT[C/G]TAGGGCTGGGCCAGC	59349
rs572705950	in-del	-/A	0.00755907	0.0610114	intron-variant	KLHL12	GRCh38.p7	1:202896196	AGACAGATACAAACT[-/A]TTTTTTTTCTGAGTT	59349
rs572762673	snp	C/T	0.0170251	0.090679	intron-variant	KLHL12	GRCh38.p7	1:202918001	AAGAAAGTGGCAAAC[C/T]CCCTCTCCATAAAAA	59349
rs572887077	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904166	TGTGCCACCAAGCCC[A/G]GCTAATTTTGTATTT	59349
rs572890227	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202923103	CTTTGAACAATTACT[C/T]TCAAAAATAAAGACA	59349
rs572972283	snp	A/G/T	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202920368	TGCTCTATTTTGTTG[A/G/T]ATTTTTTTTTTTTTT	59349
rs572988621	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202912327	TACCATCCTACGAAT[A/G]GCCATAACTGTGAAG	59349
rs573031944	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907286	TCTACATTGAACATG[C/T]AGTACTTATGCCATT	59349
rs573238090	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905851	ACTCTGTCGCCCAGG[C/T]TGGAGTGCAGTGGCG	59349
rs573280263	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202911937	ATGGGGAATGCTCAC[A/G]GACTGTGTGGTAATG	59349
rs573423334	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915982	ATTAGCTATTATATG[C/T]AGTGAACGTCAAATC	59349
rs573465418	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892387	GACGGGGAGTATGTG[C/T]CAAATAAGTACAATC	59349
rs573510592	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891792	TGCTGTCTCCAGTGC[A/G]AAAGACCTCGGGGAA	59349
rs573600040	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902344	CTGAGGCAGGAGAAT[C/T]GCTTGAACTTGGGAA	59349
rs573767086	snp	C/T	1.65201e-05	0.00287398	missense, intron-variant	KLHL12	GRCh38.p7	1:202893380	GCTGTACCATCAAAT[C/T]CCCCCACCACATAAA	59349
rs573852937	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202915228	TGAAAATTAGTGGTT[A/G]GGTAACACATGCCAC	59349
rs573864172	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202895308	TGAGGTGGGAGGATC[A/G]CTTGAGCTTGGGGAG	59349
rs573885376	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202903093	TTGAGCCCAGAAAGT[A/G]AAGTTTCAGTGAACC	59349
rs574015398	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902169	GGGCACAGTGGCTAG[C/T]GCCTGTAATCCCAGC	59349
rs574046179	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913476	ACCCCACTCTTAACT[G/T]CCAGGCACTGTCCTG	59349
rs574136835	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922765	TGCTGGGATTACAGG[A/C]GTGAGCCACCACGCC	59349
rs574218697	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929819	GTAGCAAGAGCACGC[A/C]TCAAAATATATTTAT	59349
rs574245939	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202922322	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	59349
rs574308981	in-del	-/A	0.00755907	0.0610114	intron-variant	KLHL12	GRCh38.p7	1:202925433	TCACGGAGTGTCCCT[-/A]CCACTTGACATTTAA	59349
rs574318526	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202925884	GCTGAGGTGGGTGAT[C/G]AGTTGAGGTCAGGAG	59349
rs574410679	in-del	-/A			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928312	AAAAAAAGAAAAAAC[-/A]AAAAAAAAGGCTGGA	59349
rs574481959	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202925968	AAAATAGCCAGGCGT[A/G]GTGATGCGCGCCTAT	59349
rs574502509	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202920187	GGCATGGTGGCACAT[A/G]CCTGTAGTCCCAGCT	59349
rs574597540	in-del	-/A	0.00358779	0.0422022	intron-variant	KLHL12	GRCh38.p7	1:202901059	AAAAATAAAATAAAG[-/A]AAAAACCCCTCTCTT	59349
rs574669876	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919537	GAAAAGGTGCAAATG[C/T]TCTCTTTTATAGAGC	59349
rs574706807	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202926600	AGACAGCCCGGGGGG[A/T]CTTTTATCGTTTCCG	59349
rs574842739	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202918132	AGTTTTGTAATTGCC[C/G]AATCTTGAAGAAACC	59349
rs574867610	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924044	CTGCTCTTAAAATGA[A/G]ACTTGGGATCTTGAA	59349
rs574964832	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928699	CTAATTGATTCAGGA[A/C]ATTCTAATTTATTTT	59349
rs575022942	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202904988	ATGCAGAAGAGTCAT[C/T]ATCCTGGTAGCTGGT	59349
rs575065410	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904433	CTATTTTGTGCCTAG[A/G]AAGTCCTTCTTCCCC	59349
rs575170217	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893496	ATAGAAATAAACTAC[A/G]GTCACTAATGACTAG	59349
rs575196862	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202897575	GACATAATCCTTGAG[A/G]TCTTAAGTGCAGGTG	59349
rs575240393	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202921524	TGCAGGTCATCCTAA[A/G]GGACTTTCTTATGTA	59349
rs575290556	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913925	CAGCAACACGGGGCT[A/G]GCGGGAGCAAACCAG	59349
rs575301485	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202926038	TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAGCC	59349
rs575313738	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202906316	AAAAATTAGCCAGGC[A/G]TGGTGGCACACACCT	59349
rs575317411	snp	A/C	0.00716266	0.059414	intron-variant, upstream-variant-2KB, missense	KLHL12	GRCh38.p7	1:202927505	CTGGGGATCACGGCA[A/C]AACCCCGTTTCTACA	59349
rs575325373	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202920968	GGTTATAACTCCAGT[C/T]TCTCCAGGACTACCT	59349
rs575350095	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202905947	GTAGCTTGAACTACA[A/G]GTGCCCGCCACCACA	59349
rs575436413	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202893531	GTTCTACAGTAGATG[A/G]GGGATATGGAATGGG	59349
rs575551138	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202901267	ATGTATAAAGGAGTT[C/T]GTTTTGTTCTGTTTA	59349
rs575587961	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202908538	ACGAGGTAAACTGGT[A/C]CCTGCACCAACAGTA	59349
rs575712218	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202903126	GATCATGCCACTGCA[C/T]TCTAGCCTAGGAGCC	59349
rs575749382	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202910302	TCTGTGCTCCTAAAC[A/T]CAATGTAAAGAACTA	59349
rs575751252	snp	A/C	0.0146672	0.084371	intron-variant	KLHL12	GRCh38.p7	1:202902440	GTCCAAAAAAAAAAA[A/C]ACCAAAAACAAACAA	59349
rs575765891	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202899075	CCCAACACTTTGGGA[A/G]GCCAAGGCTGGCAGA	59349
rs575796868	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202924866	CAAAACATCACACTG[C/T]AAAAATTCAAAATTA	59349
rs575857304	snp	A/T	0.0298908	0.118541	intron-variant	KLHL12	GRCh38.p7	1:202899850	AAAAAATAATAATAA[A/T]AAATAAAAAAATCAA	59349
rs575896487	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891879	TCAGTGCTGTTCTAG[A/G]TTCACTCACAATCAA	59349
rs575993100	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202896326	AAGTAGCTAGGACTA[C/T]AGGCATGCACCACCA	59349
rs576150809	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202917975	ACCCACTGGGATCAT[A/G]TATCTAATTGAAGAA	59349
rs576184688	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL12	GRCh38.p7	1:202909461	AAACACAAGTACATA[A/G]TAACTAATAAGAATT	59349
rs576190340	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202920100	AGGCAAATCACCTGA[C/G]GTCAGGAATTCAAGA	59349
rs576502580	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929911	ACACTTCGAGAGGCC[A/G]AGGCGGGCGGATCAC	59349
rs576534286	snp	C/T	0.00557542	0.0525036	intron-variant	KLHL12	GRCh38.p7	1:202917007	AAAGAATTGGACCAC[C/T]GGAGATCAATACTAT	59349
rs576565346	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202920431	TCCCAGGCTGGAGTG[C/T]AGTGGTGCCATCTCG	59349
rs576581677	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202906490	AAAAAGTTCCTACCC[C/T]GGGAGGAAAGGCAAA	59349
rs576624765	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202922644	GGCGCCCGCCACCAC[A/G]CACGGCTAATTTTTT	59349
rs576669143	in-del	-/GTTCAAGT	0.00557542	0.0525036	intron-variant	KLHL12	GRCh38.p7	1:202921106	ACCTCTGCCTCCCAG[-/GTTCAAGT]GTTTCTCGTGCCTCA	59349
rs576726932	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202919677	CTCCAAAATGTTCAT[A/G]ATTAAGTTTACACTA	59349
rs576755214	in-del	-/T	0.00279162	0.0372561	intron-variant	KLHL12	GRCh38.p7	1:202899997	TTCCCTACCTATTCC[-/T]TTTTCTTACTCCACC	59349
rs576907703	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202926784	TCGGGAGATTCGGGG[C/T]AGGGAATGGGTAGTA	59349
rs576914558	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913766	GTAAGAGAGTACTCC[A/G]AGGCAGACAGAAGAG	59349
rs576951592	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202925697	GTAAGAAAAAGTGTG[A/T]ATTCAACTTCAACTT	59349
rs577057378	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202913085	AAACAAGAAAGAAAA[A/G]CATTATCAATTAGCC	59349
rs577120654	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL12	GRCh38.p7	1:202911901	AACCAATGAAGAAAG[C/G]CTGAGGAGCTATTTT	59349
rs577294545	snp	A/G	6.59413e-05	0.00574163	synonymous-codon	KLHL12	GRCh38.p7	1:202918180	CCGTACCTGAATTTC[A/G]TCGCACTTGATTAGC	59349
rs577519655	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202908684	TTACCTGCCATTATG[C/T]GGCACTAAAATTATC	59349
rs577536834	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926474	GCAAGACCCATTTTA[C/T]AGAAAAGCGGGTGAT	59349
rs577593563	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202897823	GATTCTCCTGCCTCA[A/G]CCTCCCAAAGTGCTG	59349
rs577651821	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202907996	ACTAACACCTTAGCA[C/T]GCATCATGAGTCCTC	59349
rs577652971	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202915102	AGATTTTCTCCACAA[C/T]ACATTTTCACAAAGA	59349
rs577696550	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899935	ATTACTTCAAGTTGG[C/G]AGAAGCTAGGACCAC	59349
rs577731591	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202899572	GGCTCATGCCTGTAA[C/T]CCTAGCACTTTGGGA	59349
rs577778366	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL12	GRCh38.p7	1:202921778	ATCTTAATCTTAGTT[C/T]AGAAATTCATTTTAC	59349
rs577916674	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928896	GTGCACTGGCGCGAT[C/T]TCAGCTCACTGCAAC	59349
rs577981515	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202902285	AAATACAAAAATCAG[C/G]CAGACATGGTAGCAC	59349
rs578043946	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL12	GRCh38.p7	1:202906988	TTTTACAAAAAAGAA[A/G]AAAAAGACTTCCATC	59349
rs578046875	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202902057	GTATTATGAAAAAAA[A/T]ATTACCCATAGTTCC	59349
rs578063185	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202913762	GGGAGTAAGAGAGTA[C/T]TCCGAGGCAGACAGA	59349
rs745315081	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906718	CCAGGCTGGAGTACA[A/G]TGGTGCAATCTTGGC	59349
rs745315223	in-del	-/CAG			intron-variant	KLHL12	GRCh38.p7	1:202919148	GTGGTCCCAGCTACT[-/CAG]GAGGCTGAGGTGTGA	59349
rs745316448	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202921121	GTTCAAGTGTTTCTC[A/G]TGCCTCAGCCTCCCA	59349
rs745336661	snp	C/T	1.64795e-05	0.00287045	missense	KLHL12	GRCh38.p7	1:202911142	AAGGATTCTTCCCGC[C/T]CTTTCTTGGCATGCT	59349
rs745520626	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202919953	TGGTTATAATTCCAC[A/G]AGATAAAGGCAGAAT	59349
rs745656039	snp	A/G	1.70464e-05	0.0029194	intron-variant	KLHL12	GRCh38.p7	1:202895507	GGAAATAATTGCCCT[A/G]CACATCCAGCCTACC	59349
rs745682143	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915420	GAACAGAAAAATATA[C/T]GTCACTTGCTTTCTT	59349
rs745720689	snp	C/T	1.65094e-05	0.00287305	missense	KLHL12	GRCh38.p7	1:202894702	CATAGCGCTCCATAC[C/T]GGTGTGACGCCTGCT	59349
rs745747601	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	KLHL12	GRCh38.p7	1:202919843	GTACACAAAGTCCAA[C/T]AAAATTTCCATGGTA	59349
rs745796879	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893080	ACAGAGCAATACTCT[A/G]TCTCTAAAAAATAAA	59349
rs745808815	snp	A/G	1.66882e-05	0.00288857	intron-variant	KLHL12	GRCh38.p7	1:202919714	TTCAACCTTTCCAGG[A/G]CTATTTTGACATAAA	59349
rs746023146	snp	A/G	1.64768e-05	0.00287021	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896935	GCTTCCAAAGCCCCC[A/G]ACCACCAAAAGCACT	59349
rs746098017	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	KLHL12	GRCh38.p7	1:202925058	CTCTACTCTCAATGT[C/T]ACATCACAGAGGGTA	59349
rs746163175	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202898750	ACAGGATGGAAACTT[C/T]TGGATTAAAACGAGA	59349
rs746176907	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202913598	AGAAAAATGAACAAT[C/T]TCACTATTATTGCAT	59349
rs746191035	snp	A/T	1.68168e-05	0.00289967	intron-variant	KLHL12	GRCh38.p7	1:202924936	CTAGAGTTCCACGGG[A/T]TTCATTTGTGTGGGG	59349
rs746285996	snp	A/G	1.64806e-05	0.00287054	missense, intron-variant	KLHL12	GRCh38.p7	1:202893350	ATGTTGTATGCTTCA[A/G]CGGAAGAAAGGTGGG	59349
rs746373912	snp	G/T	1.79252e-05	0.0029937	intron-variant	KLHL12	GRCh38.p7	1:202893210	GCTCTGGCTACATAT[G/T]GAGTCTGGATTCGTT	59349
rs746542042	in-del	-/AAAC	1.6679e-05	0.00288777	intron-variant	KLHL12	GRCh38.p7	1:202894761	ATATCTGCTCAGAAT[-/AAAC]AAATTACAGACTATT	59349
rs746570202	snp	A/G	6.53616e-05	0.00571634	intron-variant	KLHL12	GRCh38.p7	1:202925219	GCAACTACAAGAGGG[A/G]AAAAAAAACAATGAG	59349
rs746633445	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202898475	TTATTTCAAAAGCCA[A/G]TATATTACTATGAGA	59349
rs746754892	snp	C/T	8.87863e-05	0.00666223	intron-variant	KLHL12	GRCh38.p7	1:202894291	TATCCTCCTGGAAGA[C/T]AGAGACCATTCCAGA	59349
rs746767687	snp	C/T	1.67497e-05	0.00289389	intron-variant	KLHL12	GRCh38.p7	1:202918436	ATAGTTGGACAGGTG[C/T]GATCTAGGATATATT	59349
rs746978187	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891791	ATGCTGTCTCCAGTG[C/T]GAAAGACCTCGGGGA	59349
rs746985573	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202907857	AGGCTGCAGTGAACC[A/G]AGATCACGCCACTGC	59349
rs747151305	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909703	ACTGTGTCAATAGGG[C/T]TTCCTATGCCTTCTA	59349
rs747152767	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202923353	AAATGCTTCTGATGA[C/T]CTTGGGTATATCTCA	59349
rs747177473	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902337	CGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC	59349
rs747234339	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202916581	CCCAGAAGGTGAAGG[C/T]TACAGTGAGCTGAGA	59349
rs747307536	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202910896	TTCGCTTTTCTTAGA[A/G]ATATGCTTGGGGACT	59349
rs747396523	snp	A/G	1.64776e-05	0.00287028	missense	KLHL12	GRCh38.p7	1:202911130	AGCAGGTTAGGCAAG[A/G]ATTCTTCCCGCTCTT	59349
rs747477655	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202922435	AGCCAGGCGTCAAGG[-/A]AAAAAAAAAAAAGAG	59349
rs747481576	snp	C/G			synonymous-codon	KLHL12	GRCh38.p7	1:202925088	ATTGCTCTTCCTGAG[C/G]GAGTTCATTGAATTG	59349
rs747535018	snp	C/T			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927342	CACGTGACCTGTCTG[C/T]ACCCTAGCGCGGGGC	59349
rs747562954	snp	A/G	1.66045e-05	0.00288132	intron-variant	KLHL12	GRCh38.p7	1:202909160	GAGTTAGGCACTGGG[A/G]ATACCTGTAATACTA	59349
rs747670995	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	KLHL12	GRCh38.p7	1:202894628	GGCCACTACGAGTCC[A/G]GCACCTTCCCGGGCT	59349
rs747680787	snp	A/G	8.86407e-05	0.00665676	synonymous-codon	KLHL12	GRCh38.p7	1:202894239	TCCTGTATGAGGGTC[A/G]TATTTCTCAACTGAA	59349
rs747781506	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202910822	TGTAAAACAGACAGC[A/C]AAACACAAAATTGAA	59349
rs747781700	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202909233	AGAAAACCAGTTTGC[-/A]AAAGCCCTGTGATTC	59349
rs747817946	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202895428	CCTTAATTTTTTCTC[C/T]GTATTTCATGCTCCT	59349
rs747825057	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202896417	GCTGGTCTTGAACTC[C/T]TGGCCTCAAGAGATC	59349
rs747867521	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905127	GCATTTCCCTTCTAG[A/G]ACTTCTGAAAAATAA	59349
rs748080354	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896869	TGGCAAAAAGCTCCA[C/T]TCCTGAGTCTTGGGG	59349
rs748100635	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202918530	AGATTAGAAATTCTA[C/T]GCTTAAGGAACTTAA	59349
rs748175504	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202900793	CGCTTGAACCTGGGA[C/G]ATGCAGGTTGCAGTG	59349
rs748178773	snp	A/G	1.64798e-05	0.00287047	synonymous-codon	KLHL12	GRCh38.p7	1:202919861	AATTTCCATGGTAGA[A/G]GCAGTCAAACCTTGG	59349
rs748263548	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902154	ACACAAATGGGGGCC[A/G]GGCACAGTGGCTAGC	59349
rs748268515	snp	G/T	6.63295e-05	0.0057585	intron-variant	KLHL12	GRCh38.p7	1:202919735	TTGACATAAACAATA[G/T]CAAGTTTTAATGTCT	59349
rs748307905	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202914012	TTCTACAGCAAAAAA[G/T]AACTGGCAGCTTGAG	59349
rs748386137	snp	C/T	3.29538e-05	0.00405904	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892587	CTGGGTTCCCATGGA[C/T]GTCACGACTTCCCAG	59349
rs748412044	snp	A/G	1.65594e-05	0.0028774	intron-variant	KLHL12	GRCh38.p7	1:202909144	AATATAGCAGACAGC[A/G]GAGTTAGGCACTGGG	59349
rs748500586	snp	C/T	1.65803e-05	0.00287922	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892483	TTTTGATTCTCCCAC[C/T]AACTGTCCACTGGAC	59349
rs748544482	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924209	CACTACCTGTATTCT[C/T]TCAAGCCAACCTTTT	59349
rs748613622	snp	A/G/T	4.94306e-05	0.00497124	missense	KLHL12	GRCh38.p7	1:202909024	CCTAGGCGAGCCCTT[A/G/T]TCCTGGGTCCCTGCA	59349
rs748739319	in-del	-/AT			intron-variant	KLHL12	GRCh38.p7	1:202919653	CAAACATGAACATCC[-/AT]AGTTTGTCTCCAAAA	59349
rs748779851	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202916874	AGCTACACAGGAGGA[-/T]GAGGTGGGAGAGCTG	59349
rs748796274	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929711	GTTCAGAGCCTGGTG[C/T]GGTGGTGTACACCTA	59349
rs748842460	in-del	-/A			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927674	AGAATGAGACCCTGT[-/A]AAAAAAAAAAAAAAA	59349
rs748878281	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202923049	TATACAGAATTGCTA[A/C]GAGAACTAAGCCTAG	59349
rs749024855	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202917118	CTCTGCTACTGGTAC[G/T]CTGATTTAGAATTAG	59349
rs749111676	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202903772	GGATTACAGGCATGC[A/G]TCACCATGCCTGGCT	59349
rs749228480	snp	C/T	1.65999e-05	0.00288091	missense, intron-variant	KLHL12	GRCh38.p7	1:202895537	CTCCCAGGGTGGTGG[C/T]TCCAGCAAGACCTCG	59349
rs749295165	snp	A/G	3.29544e-05	0.00405908	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892571	CACCAGCATCACAGC[A/G]CTGGGTTCCCATGGA	59349
rs749408890	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202913743	TGAGTAGCAGTTAGC[C/T]AGGGGGAGTAAGAGA	59349
rs749527658	snp	A/G	6.59446e-05	0.00574177	intron-variant	KLHL12	GRCh38.p7	1:202908995	TCCCCTCATTCTGCC[A/G]AGATACCAGCTTACC	59349
rs749595877	in-del	-/A	3.67627e-05	0.00428719	intron-variant	KLHL12	GRCh38.p7	1:202894330	TAAATCCTCATGCCC[-/A]TTCCTGGTCGGTTTT	59349
rs749703275	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202921302	GCCTCAGCCGCCTGA[A/G]TAGCTGGGACTACAG	59349
rs749714699	snp	G/T	1.64732e-05	0.0028699	missense	KLHL12	GRCh38.p7	1:202925078	CACAGAGGGTATTGC[G/T]CTTCCTGAGGGAGTT	59349
rs749733481	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202900602	GGCGTGGTGGCTCAC[A/G]CCTGTAATCACAGCA	59349
rs749832286	snp	A/G	9.08967e-05	0.00674093	missense	KLHL12	GRCh38.p7	1:202894207	TTGGTGGCCATTGGT[A/G]TAACATTAGTCCAAT	59349
rs749871310	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202908305	CTTGCCCAACCAGTC[A/G]TTGCTGGGGCTTGGA	59349
rs749876703	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202901787	TTTTGATAACTATGA[C/G]AGCAACAGTGTTTCA	59349
rs749976867	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202922826	TTAGCTAGTAAGAGA[C/G]AGATATCATTCTTAT	59349
rs750058530	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915991	TATATGTAGTGAACG[C/T]CAAATCTGTAGTGCT	59349
rs750065681	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202910685	TTCATGCTGGCTTTA[A/C]CAGAAGTCAAAAATG	59349
rs750075682	snp	A/C	1.64876e-05	0.00287116	missense, intron-variant	KLHL12	GRCh38.p7	1:202895654	GGCCATCATAGCCAC[A/C]AATGACGTAGATCCG	59349
rs750122033	snp	C/T	8.24029e-05	0.00641831	missense	KLHL12	GRCh38.p7	1:202924999	GCACAGAAGTAATCA[C/T]TACAGGCAGCCAGCA	59349
rs750254391	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202896151	TCAGAAATTACTATT[A/G]TTCATTCAGCACTGA	59349
rs750328114	snp	A/G	1.67595e-05	0.00289473	missense, intron-variant	KLHL12	GRCh38.p7	1:202893264	CATAGAGTCTCCCCC[A/G]AAGCACTGTGGCCCC	59349
rs750359660	in-del	-/C			intron-variant	KLHL12	GRCh38.p7	1:202899651	TCTAACATGGCAAAA[-/C]CCCGTCTCTACTAAA	59349
rs750362890	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909153	GACAGCAGAGTTAGG[C/T]ACTGGGGATACCTGT	59349
rs750368622	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924011	TTGAAAAAATAAATC[A/G]AGATAATTTATTTAA	59349
rs750397673	snp	A/T	1.66557e-05	0.00288575	intron-variant	KLHL12	GRCh38.p7	1:202892684	AAAGAAGCAAAAGAA[A/T]GAAATGAGTCAGCTG	59349
rs750485982	snp	C/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891409	AAAATCTACACTAAA[C/G]GACAGGTAAGGAAAA	59349
rs750512668	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907026	TATACAAATATTTTC[C/T]TATAATTTCTTCTAA	59349
rs750638252	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917509	GCCACTGCACCTGGC[C/T]TACTATTCCTTTAAC	59349
rs750663868	snp	C/T	3.29636e-05	0.00405964	intron-variant	KLHL12	GRCh38.p7	1:202894572	GTTCCCTCCCATTCC[C/T]GCATCCCAGACTCAA	59349
rs750693407	snp	C/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891480	TACAAACCACTCCTT[C/G]GCAGACATGTGCTTC	59349
rs750753403	snp	C/G	9.65391e-05	0.00694696	intron-variant	KLHL12	GRCh38.p7	1:202894144	TATGTAAAGGTCTGA[C/G]AGCATCGCCTATTGT	59349
rs750771168	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914733	TAGCCAGGTGTGGTG[C/T]GCACGCCTGTGGTCC	59349
rs750847706	snp	A/G	1.64738e-05	0.00286995	stop-gained	KLHL12	GRCh38.p7	1:202918263	CAGGAAAATGCTTCT[A/G]GCTAAAAACCTCAGC	59349
rs750948732	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926696	CAAGTCTCAGCATAT[C/T]CTTCATCCTCACCCT	59349
rs751081191	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202901121	AAGGGTGGGAGAAAA[C/G]AAGTAGAAAGGAAAT	59349
rs751086647	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202895616	TGTGTAGTCTAGACA[C/T]TCCACTGAACTAAGG	59349
rs751141092	snp	A/C	1.66125e-05	0.00288201	intron-variant	KLHL12	GRCh38.p7	1:202919920	AGAGCTGAAAATTCA[A/C]AAGGTATAAAAGAAT	59349
rs751151515	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905866	CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTTACT	59349
rs751176821	snp	C/T	1.7336e-05	0.00294409	intron-variant	KLHL12	GRCh38.p7	1:202895472	AGAGGTTAAAAACCC[C/T]GGTCCAGCCACAGTA	59349
rs751279335	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914447	CTTAAAACTTTTATA[C/T]GATTGGAAAATAGTT	59349
rs751279414	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202900221	TATAACTCCCTGCCC[C/T]ACCCCCCAACCCCCC	59349
rs751306766	snp	C/T	1.65042e-05	0.0028726	missense, synonymous-codon	KLHL12	GRCh38.p7	1:202892649	TACTTAGCAGGGAAT[C/T]ACCATCATATCTGAG	59349
rs751453489	snp	A/G	4.94735e-05	0.00497336	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892542	CAATGGTCACTTCTC[A/G]CGGAGAACACAAACA	59349
rs751476466	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202921618	ATTGTTAGCAGTATA[-/T]TTAGTCTAAATTGTT	59349
rs751488344	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202912673	CCAAACCACGAAACC[-/A]AGGTGGCTATGGTGG	59349
rs751490390	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202919659	TGAACATCCATAGTT[G/T]GTCTCCAAAATGTTC	59349
rs751525786	snp	C/T			synonymous-codon	KLHL12	GRCh38.p7	1:202918228	ACTCAGAAGAATGAA[C/T]TCTTCATGCTGTACC	59349
rs751549631	snp	A/T	1.64754e-05	0.00287009	missense	KLHL12	GRCh38.p7	1:202909081	TGAAACTTCTTTGCT[A/T]CATCAACCAGATCCC	59349
rs751612295	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202904731	GGGAAGGGGAGTGTG[C/T]GTGTGCTGTGACACG	59349
rs751660242	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202919134	GGTGGCATGCACCTG[A/T]GGTCCCAGCTACTCA	59349
rs751671183	snp	C/T	3.49125e-05	0.00417792	intron-variant	KLHL12	GRCh38.p7	1:202893461	AGCAAATGTATGGTA[C/T]TAAGCCTAGAATCTG	59349
rs751780981	in-del	-/A	1.6599e-05	0.00288084	intron-variant	KLHL12	GRCh38.p7	1:202919919	GAGAGCTGAAAATTC[-/A]AAAGGTATAAAAGAA	59349
rs751815195	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	KLHL12	GRCh38.p7	1:202918246	TTCATGCTGTACCAC[C/T]TCAGGAAAATGCTTC	59349
rs751842625	snp	C/T	1.64798e-05	0.00287047	missense, intron-variant	KLHL12	GRCh38.p7	1:202893338	GAATCAGTGCGAATG[C/T]TGTATGCTTCAACGG	59349
rs751878042	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892263	AAATGACAGGAAAGT[A/G]CTCCCCAAAGCAGTG	59349
rs751895202	snp	C/T	4.98965e-05	0.00499457	intron-variant	KLHL12	GRCh38.p7	1:202911247	TCCTACTTTTCCAAT[C/T]AGCTCACCATCTCAA	59349
rs751898555	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926607	CCGGGGGGTCTTTTA[C/T]CGTTTCCGTGTCAAA	59349
rs752216707	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202913157	AGATATATTTAATTA[A/T]TCATCTGGGGAACTT	59349
rs752229257	snp	C/T	1.64803e-05	0.00287052	missense	KLHL12	GRCh38.p7	1:202919790	GCTGCAGGAAGCAGT[C/T]CTTGTACATTCTCCA	59349
rs752324875	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202925436	CGGAGTGTCCCTACC[A/G]CTTGACATTTAATAT	59349
rs752332039	in-del	-/AA			intron-variant	KLHL12	GRCh38.p7	1:202899832	CATCTCAAAAAAAAA[-/AA]AAAAAAATAATAATA	59349
rs752399607	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	KLHL12	GRCh38.p7	1:202909062	CCGAAGTTCAGGCCT[C/T]AGATGAAACTTCTTT	59349
rs752416960	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926550	GCAACTCTAGGGGTG[C/T]AAAAAGGTCTAGAAC	59349
rs752416977	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202911970	AGACCCAAACACCAA[A/G]TGCTCCAGGGGCTTT	59349
rs752509085	in-del	-/GTAA			intron-variant	KLHL12	GRCh38.p7	1:202918093	TATGAAGCCCTGATG[-/GTAA]GTAACTGCATCCTAT	59349
rs752543644	snp	A/C	1.65157e-05	0.0028736	intron-variant	KLHL12	GRCh38.p7	1:202908964	GTTGTCACCTGCAAG[A/C]AGTAGTTGAAAAGCA	59349
rs752563420	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202920844	ATTAAAATACAGATG[A/T]ATTTACAGAATAGAA	59349
rs752680158	snp	A/C	1.64817e-05	0.00287064	stop-gained	KLHL12	GRCh38.p7	1:202925159	GGGCCATAATGCCTC[A/C]CATAAAGCAGTGCGG	59349
rs752706995	in-del	-/A	0.00147468	0.0271139	intron-variant	KLHL12	GRCh38.p7	1:202925219	GCAACTACAAGAGGG[-/A]AAAAAAAACAATGAG	59349
rs752742787	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202916445	ATGTCAGGAGTTCCA[C/G]AGCAGCCTGGCCACA	59349
rs752775817	snp	C/T	1.65941e-05	0.00288041	intron-variant	KLHL12	GRCh38.p7	1:202911226	TGTATAATTACACAC[C/T]GTGGATCCTACTTTT	59349
rs752883632	snp	C/T	1.70679e-05	0.00292124	intron-variant	KLHL12	GRCh38.p7	1:202892710	AGCTGCGTGCAGTGG[C/T]ACGTGCCTGTAATCC	59349
rs752905625	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202899124	TTGAGACCAGCCTAG[A/C]CAACAAGGCAAAACC	59349
rs752920483	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202895899	ACTGAACGAAATGCC[C/T]GTTGTGGTGCTCTTA	59349
rs752925123	snp	G/T			missense	KLHL12	GRCh38.p7	1:202894208	TGGTGGCCATTGGTG[G/T]AACATTAGTCCAATG	59349
rs753043000	in-del	-/TC			intron-variant	KLHL12	GRCh38.p7	1:202911456	ATATATATATATGTA[-/TC]TCTCTCTCTCTCTCT	59349
rs753124636	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905531	ATGTCTTATCTCCTA[A/G]TGCCAGGTTCTTTCC	59349
rs753172357	snp	C/T	3.3465e-05	0.0040904	intron-variant	KLHL12	GRCh38.p7	1:202894768	CTCAGAATAAACAAA[C/T]TACAGACTATTAGAG	59349
rs753219420	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917966	GTGATTCTTACCCAC[C/T]GGGATCATATATCTA	59349
rs753226802	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903078	AGGTGGGAGGATTGC[C/T]TGAGCCCAGAAAGTG	59349
rs753233771	in-del	-/GTGGCAC	3.38424e-05	0.0041134	intron-variant	KLHL12	GRCh38.p7	1:202892706	AGTCAGCTGCGTGCA[-/GTGGCAC]GTGCCTGTAATCCCA	59349
rs753313109	snp	C/T	3.30147e-05	0.00406279	synonymous-codon, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202925172	TCCCATAAAGCAGTG[C/T]GGAGAAAGAACAAAA	59349
rs753314178	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904301	AAGGCACCCTGCCAG[A/G]CCAACCCTTTAACCC	59349
rs753407736	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202910748	TTGGAACAATTTATG[C/T]TTAATGGAGAAGGGG	59349
rs753493316	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904088	CAATGGCACGATCTT[A/G]GTTCACCACAATCTC	59349
rs753607460	snp	C/G	1.64743e-05	0.00287	intron-variant	KLHL12	GRCh38.p7	1:202896843	CAACGAATGGTTTCA[C/G]CATTATTTACTGGCA	59349
rs753607650	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	KLHL12	GRCh38.p7	1:202925136	AGTATTTGTCATTAT[A/G]TCTTTGGGGGCCATA	59349
rs753632801	in-del	-/CTG			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892335	TTTTTCCTGGAATAT[-/CTG]CTGTTACCCACCCTT	59349
rs753698311	snp	G/T	1.64757e-05	0.00287012	missense	KLHL12	GRCh38.p7	1:202925018	AGGCAGCCAGCACAA[G/T]CCGATGGGCAGGGAA	59349
rs753812432	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902378	GAGACTGCAGTGAGC[C/T]GAGATCACACCATTG	59349
rs753921250	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202893913	ACTTTATTTAACAGA[C/T]ATTTATTAAGCATGT	59349
rs753939127	snp	G/T	9.90606e-05	0.00703708	intron-variant	KLHL12	GRCh38.p7	1:202911040	TTGGATCCTGAGAGT[G/T]TTGCACTACTTACCT	59349
rs754003681	snp	A/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928978	TGGGAGTACAGGTGC[A/T]CACCACCACGCCCGA	59349
rs754030830	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202907479	TGGTGGCAGTCGCCT[A/G]TTGTCCCAGCTACTC	59349
rs754074018	snp	G/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891650	GCAAACATTGCCATG[G/T]CTAGATGAGCCCTGG	59349
rs754095943	in-del	-/AAG			intron-variant	KLHL12	GRCh38.p7	1:202894065	AGAGAAAACAGAGAC[-/AAG]GAGGAGAGCAGAATC	59349
rs754118094	snp	C/T	0.000118043	0.00768163	missense, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928510	GGAACTTTTTGACAT[C/T]GAGAAAACCCACAGA	59349
rs754213512	snp	A/G	1.64749e-05	0.00287005	missense	KLHL12	GRCh38.p7	1:202894602	ATACCTAGACAGTAG[A/G]TCACTCCACTGGCCA	59349
rs754274931	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202908909	GAAAAGGTCTGAAAC[A/G]AGGTGTCTGTACTTC	59349
rs754305311	snp	C/G	0.000314801	0.012542	intron-variant	KLHL12	GRCh38.p7	1:202918408	GACAGACACAGGCAG[C/G]AAACACTTTAGAATA	59349
rs754379195	snp	A/G	1.73718e-05	0.00294714	synonymous-codon	KLHL12	GRCh38.p7	1:202894212	GGCCATTGGTGTAAC[A/G]TTAGTCCAATGTCCT	59349
rs754396941	in-del	-/TCTCTC			intron-variant	KLHL12	GRCh38.p7	1:202911457	ATATATATATATGTA[-/TCTCTC]TCTCTCTCTCTCTCT	59349
rs754469300	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	KLHL12	GRCh38.p7	1:202918282	AAAAACCTCAGCTGC[C/T]TGCATCAGGTCAACA	59349
rs754499732	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202896367	ATTTTTTTGTTTACT[G/T]TTTTGTAGAGACAGA	59349
rs754598827	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924773	TAACCATGTGTTACA[C/T]ATTACTATTATCCCT	59349
rs754637326	in-del	-/AAAAAAAA			intron-variant	KLHL12	GRCh38.p7	1:202899826	AGACTCCATCTCAAA[-/AAAAAAAA]AAAAAAATAATAATA	59349
rs754640403	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924146	TACTATACATTTCAA[A/G]TATTTTGTCAGGCAA	59349
rs754734043	snp	A/C	1.65825e-05	0.00287941	intron-variant	KLHL12	GRCh38.p7	1:202918412	GACACAGGCAGCAAA[A/C]ACTTTAGAATAGTTG	59349
rs754787664	snp	A/C	1.64727e-05	0.00286986	missense, intron-variant	KLHL12	GRCh38.p7	1:202896859	CATTATTTACTGGCA[A/C]AAAGCTCCACTCCTG	59349
rs754822367	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202919295	ATTGTAAGGGAAAAC[A/C]AACCACCTGTAATCC	59349
rs754878334	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202899841	AAAAAAAAAAAAAAA[-/T]AATAATAATAAATAA	59349
rs754879170	snp	A/G	1.64735e-05	0.00286993	missense	KLHL12	GRCh38.p7	1:202925030	CAATCCGATGGGCAG[A/G]GAAGTCTTTCTGCTC	59349
rs754879214	snp	A/G	1.65255e-05	0.00287445	missense, intron-variant	KLHL12	GRCh38.p7	1:202895680	ATCCGGTCATGAAGG[A/G]ACACTGAGGCCACAT	59349
rs754941428	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202897680	ACTCTCCTAACCTTG[C/T]CACAAAAAAAGCTAC	59349
rs754994863	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893965	TAGATATTCTAAAAC[A/G]TAGGGAGAGAACAAA	59349
rs755045797	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202919552	CTCTCTTTTATAGAG[A/C]CAAATACTCATATCT	59349
rs755057512	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928987	AGGTGCACACCACCA[C/T]GCCCGACTAATTTTT	59349
rs755095286	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891726	CCCAGTTATACTGAA[C/T]TCCCACATTGATGTC	59349
rs755130710	snp	C/T	4.95282e-05	0.00497611	intron-variant	KLHL12	GRCh38.p7	1:202911041	TGGATCCTGAGAGTG[C/T]TGCACTACTTACCTC	59349
rs755150140	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202894070	AAACAGAGACAAGGA[A/G]GAGAGCAGAATCTCA	59349
rs755157303	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892572	ACCAGCATCACAGCG[C/T]TGGGTTCCCATGGAT	59349
rs755169723	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914967	TTGTAAACACCACTG[C/T]CCTCAGACTAGCCAT	59349
rs755186933	snp	A/G			synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892545	TGGTCACTTCTCGCG[A/G]AGAACACAAACACCA	59349
rs755201509	in-del	-/TTCTT			intron-variant	KLHL12	GRCh38.p7	1:202893651	ATAAAAATGGTTCTC[-/TTCTT]TACTTTCATTAACTC	59349
rs755240900	snp	G/T	0.00011828	0.00768935	missense, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928537	CAGAGGCCTCAAATT[G/T]ATTCACGTCCATTGT	59349
rs755247295	snp	A/C	1.65053e-05	0.0028727	missense	KLHL12	GRCh38.p7	1:202909121	AACTACAGCGGATGA[A/C]AGGCTGAAATATAGC	59349
rs755401202	snp	A/C	1.6863e-05	0.00290365	missense, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202925199	AAAATGGGTCCTTGG[A/C]TTCTGCAACTACAAG	59349
rs755504307	snp	C/T	1.64735e-05	0.00286993	missense	KLHL12	GRCh38.p7	1:202894621	CTCCACTGGCCACTA[C/T]GAGTCCGGCACCTTC	59349
rs755550707	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202916327	AGTCACTAGAGAAAG[A/G]TGTAAAGAAACACTT	59349
rs755566576	snp	C/G	3.32557e-05	0.00407759	intron-variant	KLHL12	GRCh38.p7	1:202918165	AACATCAAGACAAAT[C/G]CGTACCTGAATTTCG	59349
rs755713061	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202902878	CACCTGTAGTCCCAA[C/G]TCCCAGCTACCTGGG	59349
rs755742112	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202909214	AATAATTAACTTCTG[A/G]CTACAGAAAACCAGT	59349
rs755872768	snp	A/C/T	3.29811e-05	0.00406075	missense, intron-variant	KLHL12	GRCh38.p7	1:202895660	CATAGCCACCAATGA[A/C/T]GTAGATCCGGTCATG	59349
rs755922107	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202896173	CAGCACTGAGAGACA[C/T]GCTGAGGGAGACAGA	59349
rs755925130	snp	C/T	8.33674e-05	0.00645575	intron-variant	KLHL12	GRCh38.p7	1:202919941	ATAAAAGAATGATGG[C/T]TATAATTCCACAAGA	59349
rs756016242	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924078	CAAAGATTTGCAATG[C/T]TATTTTCTGTTCAGC	59349
rs756018685	snp	A/C/T	3.29578e-05	0.00405931	missense	KLHL12	GRCh38.p7	1:202919854	CCAATAAAATTTCCA[A/C/T]GGTAGAGGCAGTCAA	59349
rs756141639	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907095	TCTTGTGTTGATATG[C/T]ATCTGTGTATAAAGC	59349
rs756175045	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891505	TGCTTCTAAAAGAAT[A/G]GGGCAGTAATCAGGT	59349
rs756289171	snp	C/T	0.000118772	0.00770531	missense, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928482	CAAGTATGTTTTACC[C/T]TCCAGGTACTGAGGA	59349
rs756328245	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926844	GAAACGAAGTCCTTC[C/T]TCCTAATACCACCAG	59349
rs756361481	in-del	-/AT			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891487	CACTCCTTGGCAGAC[-/AT]GTGCTTCTAAAAGAA	59349
rs756517742	snp	C/T	0.000186619	0.00965789	missense	KLHL12	GRCh38.p7	1:202894189	CTGGTCTTACCAGAA[C/T]GCTTGGTGGCCATTG	59349
rs756536034	in-del	-/G	0.000193592	0.00983659	intron-variant	KLHL12	GRCh38.p7	1:202894136	CATTATATATGTAAA[-/G]GGTCTGACAGCATCG	59349
rs756547151	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202901694	CTTCATTATTTTTCC[C/T]GACAGATCCTGTGTT	59349
rs756588739	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202913651	GCTATGAGACAGAAC[A/C]ACATGAGATTTCCTA	59349
rs756627787	in-del	-/A	0.00147468	0.0271139	intron-variant	KLHL12	GRCh38.p7	1:202925218	GCAACTACAAGAGGG[-/A]AAAAAAAAACAATGA	59349
rs756641797	snp	A/T	1.64738e-05	0.00286995	missense	KLHL12	GRCh38.p7	1:202918271	TGCTTCTGGCTAAAA[A/T]CCTCAGCTGCTTGCA	59349
rs756700248	snp	G/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928959	CTCAGCCTCTCCGAG[G/T]AGCTGGGAGTACAGG	59349
rs756860054	snp	A/C	1.66161e-05	0.00288232	intron-variant	KLHL12	GRCh38.p7	1:202919922	AGCTGAAAATTCAAA[A/C]GGTATAAAAGAATGA	59349
rs756879807	snp	A/G	1.64846e-05	0.0028709	missense, intron-variant	KLHL12	GRCh38.p7	1:202895639	AACTAAGGCGGGAAC[A/G]GCCATCATAGCCACC	59349
rs756887882	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202920998	TAGTTCCTATCATCT[C/G]TCCTTAGACTACTTT	59349
rs756969803	snp	A/C	1.72716e-05	0.00293862	intron-variant	KLHL12	GRCh38.p7	1:202895484	CCCTGGTCCAGCCAC[A/C]GTAAGATGGAAATAA	59349
rs757022484	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	KLHL12	GRCh38.p7	1:202919831	TACTGTTTCTGTGTA[C/T]ACAAAGTCCAATAAA	59349
rs757050363	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202894339	ATGCCCATTCCTGGT[C/T]GGTTTTTTTCTGAGT	59349
rs757070593	snp	A/C			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929326	AAAATTTTCCTTCAC[A/C]TATACTCGTGCACAT	59349
rs757077478	snp	C/T	3.30524e-05	0.00406511	intron-variant	KLHL12	GRCh38.p7	1:202909133	TGAAAGGCTGAAATA[C/T]AGCAGACAGCAGAGT	59349
rs757132164	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891979	AGATGAGTCTCTCTC[C/T]CCCTTGTCCCCAAAG	59349
rs757223517	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907869	ACCGAGATCACGCCA[C/T]TGCACTCCACCCTGG	59349
rs757223907	snp	A/C	0.000164821	0.00907652	missense	KLHL12	GRCh38.p7	1:202925160	GGCCATAATGCCTCC[A/C]ATAAAGCAGTGCGGA	59349
rs757301002	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896884	CTCCTGAGTCTTGGG[A/G]TCATATTTCTCTACC	59349
rs757317497	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202904846	CAAAAAAGGAGACAG[C/T]CACAAATTAGAAAAG	59349
rs757363997	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914201	AGTGATATGATCATA[C/T]TGATGTTTTGTAAAG	59349
rs757384843	snp	C/T	6.58903e-05	0.00573941	missense	KLHL12	GRCh38.p7	1:202925041	GCAGGGAAGTCTTTC[C/T]GCTCTACTCTCAATG	59349
rs757483499	snp	C/G			missense	KLHL12	GRCh38.p7	1:202918250	TGCTGTACCACTTCA[C/G]GAAAATGCTTCTGGC	59349
rs757484908	snp	A/C	1.74964e-05	0.00295769	intron-variant	KLHL12	GRCh38.p7	1:202893464	AAATGTATGGTACTA[A/C]GCCTAGAATCTGAAT	59349
rs757492661	snp	C/T	1.648e-05	0.0028705	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202893343	AGTGCGAATGTTGTA[C/T]GCTTCAACGGAAGAA	59349
rs757529857	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202912282	ACCTTTGATGACCAT[C/G]ACTCTGTGAATAAGA	59349
rs757608012	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202926675	GGGATTCCTGCCTCA[A/T]CACTCCAAGTCTCAG	59349
rs757637307	snp	G/T	1.66405e-05	0.00288443	intron-variant	KLHL12	GRCh38.p7	1:202911249	CTACTTTTCCAATTA[G/T]CTCACCATCTCAAAA	59349
rs757703466	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	KLHL12, RABIF	GRCh38.p7	1:202891096	CTACTAAAGGCAATG[C/T]TGGTTAGCCACAAAC	59349
rs757726980	snp	G/T	1.64781e-05	0.00287033	missense	KLHL12	GRCh38.p7	1:202911133	AGGTTAGGCAAGGAT[G/T]CTTCCCGCTCTTTCT	59349
rs757911716	snp	C/T	5.01953e-05	0.00500951	intron-variant	KLHL12	GRCh38.p7	1:202894769	TCAGAATAAACAAAT[C/T]ACAGACTATTAGAGA	59349
rs757999772	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	KLHL12	GRCh38.p7	1:202919807	TTGTACATTCTCCAC[C/T]GTCACATGTACTGTT	59349
rs758020285	in-del	-/TAGG			intron-variant	KLHL12	GRCh38.p7	1:202926542	ACTTAGTTGCAACTC[-/TAGG]GGTGTAAAAAGGTCT	59349
rs758052074	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202912133	TTAACTGTGAAAAAG[A/G]TATTTGTTGGCAGCA	59349
rs758092268	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202920957	AGGAGCCTGTGGGTT[A/G]TAACTCCAGTCTCTC	59349
rs758259893	snp	A/G	4.95511e-05	0.00497726	intron-variant	KLHL12	GRCh38.p7	1:202908968	TCACCTGCAAGAAGT[A/G]GTTGAAAAGCATCCC	59349
rs758465114	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202916478	AGTGAAACTCCGTCT[C/T]TGCTAAAAATACAAA	59349
rs758557076	snp	C/G	1.64795e-05	0.00287045	missense, intron-variant	KLHL12	GRCh38.p7	1:202893329	GTTGTCCAGGAATCA[C/G]TGCGAATGTTGTATG	59349
rs758600116	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202903311	TCTCTGACACTCTGG[A/T]AGGCAAAAAATTATG	59349
rs758641282	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202896116	CTTAAAAGGTAGGAG[G/T]GTTGGATTTCCATGT	59349
rs758691818	snp	C/T	1.79703e-05	0.00299747	intron-variant	KLHL12	GRCh38.p7	1:202893194	GATCACATAGACTCT[C/T]GCTCTGGCTACATAT	59349
rs758732222	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924295	TCAACGCCTGTACAG[C/T]TATTCATTAAAAACT	59349
rs758813870	in-del	-/G			intron-variant	KLHL12	GRCh38.p7	1:202893628	CTTGAAATGATAAAA[-/G]ATAAATAATAAAAAT	59349
rs758824454	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202925510	GTAAATCTTGACAAG[A/G]TTCTTGTCTCAAATG	59349
rs758828609	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202911473	CTCTCTCTCTCTCTC[G/T]CTCTCTAAGATAGAT	59349
rs758876070	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202914002	AACAGCTCTGTTCTA[C/T]AGCAAAAAAGAACTG	59349
rs758970747	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202904302	AGGCACCCTGCCAGG[A/C]CAACCCTTTAACCCT	59349
rs759002174	snp	A/G	3.29554e-05	0.00405914	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892608	GACTTCCCAGCTGTC[A/G]ATGATAGGGTCATAA	59349
rs759018927	snp	A/G			downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890892	CAAGTAACTCCAAGC[A/G]TCAGAGGGGCTAATG	59349
rs759025544	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202915324	CTTCCCATTGTTTTA[A/G]GTACTATTATTTTAT	59349
rs759096127	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202926438	TCTATAAGCACTATA[A/G]ATAATTCCTCCAACA	59349
rs759208003	in-del	-/CTTCTGACTTT			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930389	AGGAACTAGTTCAGA[-/CTTCTGACTTT]CTTCTGACTTTTTTC	59349
rs759250314	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202905322	CATTAGCTTTTAGTT[C/G]AATTTAATAAGCAAA	59349
rs759257866	snp	C/T	3.30617e-05	0.00406568	intron-variant	KLHL12	GRCh38.p7	1:202897012	GCATCCCTGGATGGG[C/T]AACTAGTCACAGGGA	59349
rs759347713	snp	C/T	1.64751e-05	0.00287007	missense	KLHL12	GRCh38.p7	1:202925141	TTGTCATTATGTCTT[C/T]GGGGGCCATAATGCC	59349
rs759407862	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202900939	TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG	59349
rs759503243	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202905115	GAAACTGCTTCAGCA[C/T]TTCCCTTCTAGAACT	59349
rs759526552	snp	A/C	3.67762e-05	0.00428798	intron-variant	KLHL12	GRCh38.p7	1:202894320	GAAAGAGTGGTAAAT[A/C]CTCATGCCCATTCCT	59349
rs759558651	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906701	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC	59349
rs759590208	in-del	-/AGGT	1.66101e-05	0.0028818	intron-variant	KLHL12	GRCh38.p7	1:202919922	AGCTGAAAATTCAAA[-/AGGT]ATAAAAGAATGATGG	59349
rs759622136	snp	A/T	1.65567e-05	0.00287716	intron-variant	KLHL12	GRCh38.p7	1:202911207	TTCAGAATCCACCTG[A/T]AAATGTATAATTACA	59349
rs759643929	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202895846	TCATGAACCCTCCTT[A/C]AGTGGTTCATCCTCA	59349
rs759713417	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202923249	TGACAAAAAACAGGA[C/T]GCACAACATATAATT	59349
rs759799894	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202908812	ATTTCCAAATAATTA[C/T]GTGAAGTAGATAGAG	59349
rs759902237	snp	A/T	1.64841e-05	0.00287085	missense, intron-variant	KLHL12	GRCh38.p7	1:202895579	TAGGGGCCACAGAAT[A/T]CCAGACCCCATCCTC	59349
rs759956130	snp	C/G	1.64906e-05	0.00287142	missense	KLHL12	GRCh38.p7	1:202919762	GTCTGTACCTTTCAA[C/G]TGAAGCAGACAGGCT	59349
rs759990156	snp	C/T	3.3012e-05	0.00406262	synonymous-codon	KLHL12	GRCh38.p7	1:202919894	GTCAACATAAGGTTT[C/T]CCCTTCTCTGAGAGC	59349
rs760062306	snp	G/T	3.29484e-05	0.00405871	missense	KLHL12	GRCh38.p7	1:202909042	CTGGGTCCCTGCATC[G/T]GACTCCGAAGTTCAG	59349
rs760136279	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905198	CTTAAGGTCAGGGCA[A/G]TAAGCAAGTTCTCTA	59349
rs760178156	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904080	CTGGAGTGCAATGGC[A/G]CGATCTTGGTTCACC	59349
rs760272199	in-del	-/G			intron-variant	KLHL12	GRCh38.p7	1:202897971	CAACAAAAGACTAGA[-/G]TTTTAAAGGAAAAGT	59349
rs760281955	snp	A/C	3.30311e-05	0.0040638	intron-variant	KLHL12	GRCh38.p7	1:202897001	GGGTTAGTTCAGCAT[A/C]CCTGGATGGGTAACT	59349
rs760314501	snp	C/T	1.64741e-05	0.00286998	missense	KLHL12	GRCh38.p7	1:202925130	AGCATGAGTATTTGT[C/T]ATTATGTCTTTGGGG	59349
rs760396388	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	KLHL12	GRCh38.p7	1:202925004	GAAGTAATCACTACA[A/G]GCAGCCAGCACAATC	59349
rs760403190	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917674	TTCTTCTTTCTTCTA[C/T]GTAATGTCCTTACTT	59349
rs760472119	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202926273	TTACTGTTAAAGAAT[A/C]GATATTGGAATCCAA	59349
rs760589125	snp	A/G	1.7013e-05	0.00291654	intron-variant	KLHL12	GRCh38.p7	1:202893429	CTACTCCTGCACCTG[A/G]GGAAAATGAATGCAT	59349
rs760658101	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202922800	GAAGATCCAAGACTT[-/A]AACCAGTCACTTAGC	59349
rs760675167	snp	A/G	1.64784e-05	0.00287035	synonymous-codon	KLHL12	GRCh38.p7	1:202918189	AATTTCGTCGCACTT[A/G]ATTAGCTTTTCCACC	59349
rs760677247	snp	C/T	3.30327e-05	0.0040639	missense, intron-variant	KLHL12	GRCh38.p7	1:202893290	GCCCCTACATAGCAT[C/T]GTGGAGTGGTCATAC	59349
rs760784295	snp	C/T	1.64928e-05	0.00287161	missense, intron-variant	KLHL12	GRCh38.p7	1:202895564	CTCGTCGGACATTCA[C/T]AGGGGCCACAGAATA	59349
rs760835503	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202919405	CAGATAGATAAAGAG[C/T]ATCCATGTAGGCTAT	59349
rs760900918	snp	C/T	1.6588e-05	0.00287988	missense	KLHL12	GRCh38.p7	1:202894740	AAGCCTCCAGAGACA[C/T]AGATCATATCTGCTC	59349
rs760985752	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202911421	GGGTTAAAAAAAAAA[-/T]ATATATATATACACA	59349
rs760991951	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202916011	TCTGTAGTGCTCATT[C/G]TATTCATTGTATTTT	59349
rs760996202	snp	C/T	1.65455e-05	0.00287619	intron-variant	KLHL12	GRCh38.p7	1:202918401	CACCTAGGACAGACA[C/T]AGGCAGCAAACACTT	59349
rs761002302	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893845	AGCCTGCTCCACTTC[A/G]AAAAGCTCTTGGTGA	59349
rs761061209	snp	C/T	1.65269e-05	0.00287457	intron-variant	KLHL12	GRCh38.p7	1:202919746	AATAGCAAGTTTTAA[C/T]GTCTGTACCTTTCAA	59349
rs761100558	snp	C/G	1.65707e-05	0.00287838	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892495	CACTAACTGTCCACT[C/G]GACTGGTCACTAGCT	59349
rs761160553	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893732	GGTGGCAATAAAGGT[A/G]GATGGAGGGAAAGGA	59349
rs761210087	in-del	-/AA			intron-variant	KLHL12	GRCh38.p7	1:202898222	CTTTTTTCAAAGAGC[-/AA]AGTCTCTTTGAGAAA	59349
rs761292901	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891369	GGATTTTGGTTGTCC[C/T]TGATTATTCTGTCCT	59349
rs761350454	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902603	AAACAATCACATAAA[C/T]AACCCTGTGATAAAT	59349
rs761368712	snp	A/G	1.64817e-05	0.00287064	intron-variant	KLHL12	GRCh38.p7	1:202896809	GGAGGCAGAGACTGA[A/G]GACATTTAACATCCC	59349
rs761439071	snp	A/G	1.64972e-05	0.00287199	missense	KLHL12	GRCh38.p7	1:202924981	ACCTCACTAGTGAAC[A/G]TGGCACAGAAGTAAT	59349
rs761466023	snp	A/G	1.73803e-05	0.00294785	missense, intron-variant	KLHL12	GRCh38.p7	1:202893242	CTAAATCCTCACCCT[A/G]CAATTGCATAGAGTC	59349
rs761706946	snp	C/G	1.6549e-05	0.0028765	intron-variant	KLHL12	GRCh38.p7	1:202892662	ATTACCATCATATCT[C/G]AGTGGGAAAGAAGCA	59349
rs761722463	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903930	GCCCTGTCTCATGCA[C/T]TCTTATGAGCTCTTT	59349
rs761740671	snp	C/T	1.65012e-05	0.00287234	synonymous-codon	KLHL12	GRCh38.p7	1:202911177	CCAGTTGATGACAGC[C/T]TCAAAGACTGGCTCT	59349
rs761748821	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202910090	AATAAATAGTAGTAA[A/C]CACTTATGTACAAAG	59349
rs761830667	snp	C/T	1.65266e-05	0.00287455	intron-variant	KLHL12	GRCh38.p7	1:202911032	TCAAGGTTTTGGATC[C/T]TGAGAGTGTTGCACT	59349
rs761836218	snp	C/T	1.64879e-05	0.00287118	intron-variant	KLHL12	GRCh38.p7	1:202894561	TTACCCATTGAGTTC[C/T]CTCCCATTCCTGCAT	59349
rs761840775	in-del	-/TAAC	1.64762e-05	0.00287016	frameshift-variant	KLHL12	GRCh38.p7	1:202911091	TATACCTGGGGGTTA[-/TAAC]GTAGGGGCATCCGCA	59349
rs761895301	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202906456	GCAACGCTTCGTCTC[-/A]AAAAAAAAAAAAAAA	59349
rs762103315	snp	A/T	1.64735e-05	0.00286993	synonymous-codon	KLHL12	GRCh38.p7	1:202918249	ATGCTGTACCACTTC[A/T]GGAAAATGCTTCTGG	59349
rs762116855	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202899281	AGCGCCACTACACTC[C/T]AGCCTGGGCAATAAG	59349
rs762136459	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202919303	GGAAAACAAACCACC[C/T]GTAATCCTGTGAAAA	59349
rs762301676	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202921497	TGCATTTAGTAATGA[C/T]GAAAAAGAACATGCA	59349
rs762357759	in-del	-/TTCCT			intron-variant	KLHL12	GRCh38.p7	1:202924315	CATTAAAAACTCTTC[-/TTCCT]TTCATTTGAAGTTAT	59349
rs762374851	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906942	GCTGGGATTACAGGT[A/G]TGAGACACCGTGCCC	59349
rs762413525	in-del	-/G			intron-variant	KLHL12	GRCh38.p7	1:202926124	AAAAAAAAAAAAAAA[-/G]AAACTTCAATTGAGG	59349
rs762421379	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202892872	CCTTTCCACACAAGT[C/T]CTTCATTAAGGCTGC	59349
rs762482656	snp	A/C	1.65589e-05	0.00287736	splice-acceptor-variant	KLHL12	GRCh38.p7	1:202919909	CCCCTTCTCTGAGAG[A/C]TGAAAATTCAAAAGG	59349
rs762514226	snp	A/G	1.77972e-05	0.002983	intron-variant	KLHL12	GRCh38.p7	1:202893223	ATTGAGTCTGGATTC[A/G]TTTCTAAATCCTCAC	59349
rs762601246	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202926557	TAGGGGTGTAAAAAG[G/T]TCTAGAACAAATGTC	59349
rs762605028	snp	A/G	1.64933e-05	0.00287165	synonymous-codon	KLHL12	GRCh38.p7	1:202892643	CAATGCTACTTAGCA[A/G]GGAATTACCATCATA	59349
rs762614670	snp	C/G			downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890896	TAACTCCAAGCGTCA[C/G]AGGGGCTAATGAATA	59349
rs762759632	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909944	ATTAAAAAAAACTCT[C/T]CTAAAATTGTCCTGT	59349
rs762792577	in-del	-/G	1.6946e-05	0.00291079	intron-variant	KLHL12	GRCh38.p7	1:202918123	CTATTTGCAAGTTTT[-/G]TAATTGCCCAATCTT	59349
rs762794430	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202901006	AGCCGAGATCATGCC[A/G]CTACACTCCAGCCTG	59349
rs762859511	snp	C/T	1.64743e-05	0.00287	synonymous-codon	KLHL12	GRCh38.p7	1:202909071	AGGCCTCAGATGAAA[C/T]TTCTTTGCTTCATCA	59349
rs762871580	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915697	GACTCTGGAGCCAGA[C/T]TACTCGAATTTGAAA	59349
rs762880874	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202897113	AATCATAAGGCTGTC[G/T]AATGGGGAGTTATTT	59349
rs762905234	snp	C/T	1.73057e-05	0.00294152	intron-variant	KLHL12	GRCh38.p7	1:202893452	GAATGCATTAGCAAA[C/T]GTATGGTACTAAGCC	59349
rs762987538	snp	A/G	1.64743e-05	0.00287	missense	KLHL12	GRCh38.p7	1:202918221	CTCCTTGACTCAGAA[A/G]AATGAACTCTTCATG	59349
rs762995740	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202899247	AACCCAGGAAGTGGA[A/G]GTTGTAGTGAGCTGA	59349
rs763045629	snp	C/T	1.64749e-05	0.00287005	missense	KLHL12	GRCh38.p7	1:202918329	CAAAATCCCTAATAC[C/T]CAGGCAATTAGAAGG	59349
rs763121009	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202898834	TTTGAACAACATAAG[C/T]ACTCAAAAACAAACA	59349
rs763156839	in-del	-/TCTC			intron-variant	KLHL12	GRCh38.p7	1:202911459	ATATATATATGTATC[-/TCTC]TCTCTCTCTCTCTCT	59349
rs763268602	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924881	TAAAAATTCAAAATT[A/G]TATCAAACTTCCACT	59349
rs763448455	in-del	-/AAAC			intron-variant	KLHL12	GRCh38.p7	1:202898841	AACATAAGTACTCAA[-/AAAC]AAACAACAAAAAATT	59349
rs763454909	snp	A/T	1.86816e-05	0.00305622	intron-variant	KLHL12	GRCh38.p7	1:202895764	TTTCAGTTAGGCAAG[A/T]TTTGGGCCTTACCTT	59349
rs763518863	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202919035	TGGGAGGATCACTCG[A/G]GCCCACGAGCTTGAG	59349
rs763536806	snp	A/G	1.64798e-05	0.00287047	missense, intron-variant	KLHL12	GRCh38.p7	1:202895599	ACCCCATCCTCATCT[A/G]CTGTGTAGTCTAGAC	59349
rs763544689	snp	C/T	1.66871e-05	0.00288847	intron-variant	KLHL12	GRCh38.p7	1:202924952	TTCATTTGTGTGGGG[C/T]TAATTTACCACTTAC	59349
rs763559351	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202918757	TCTACATGAAAACTT[A/C]CTAAAAGACTAGAGT	59349
rs763714046	snp	G/T	1.65935e-05	0.00288036	intron-variant	KLHL12	GRCh38.p7	1:202919917	CTGAGAGCTGAAAAT[G/T]CAAAAGGTATAAAAG	59349
rs763747560	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202926591	TTACTATGAAGACAG[C/G]CCGGGGGGTCTTTTA	59349
rs763797716	snp	C/T	1.64789e-05	0.0028704	missense	KLHL12	GRCh38.p7	1:202919814	TTCTCCACTGTCACA[C/T]GTACTGTTTCTGTGT	59349
rs763863176	snp	A/G	1.64944e-05	0.00287175	missense	KLHL12	GRCh38.p7	1:202892645	ATGCTACTTAGCAGG[A/G]AATTACCATCATATC	59349
rs763877169	snp	A/G	1.65217e-05	0.00287412	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892525	TCTGGATGGTGCTCC[A/G]ACAATGGTCACTTCT	59349
rs763893056	snp	C/T	1.64751e-05	0.00287007	missense	KLHL12	GRCh38.p7	1:202909076	TCAGATGAAACTTCT[C/T]TGCTTCATCAACCAG	59349
rs763950903	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202901105	ATTCAGGCACCTTTT[A/G]AAGGGTGGGAGAAAA	59349
rs763957361	snp	A/G	1.65474e-05	0.00287636	intron-variant	KLHL12	GRCh38.p7	1:202911019	AGGTAAGAGTCCGTC[A/G]AGGTTTTGGATCCTG	59349
rs764021448	in-del	-/CATTCTTGTTTTTTTTTTCTTTTTTGAGACAAGGTCTTGCTCTGC			intron-variant	KLHL12	GRCh38.p7	1:202903453	ATTGTTTCTCTCATG[lengthTooLong]TGCCCAGGCTAGAGT	59349
rs764103704	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902198	GCACTTTGGGAGGCT[A/G]AGATGAGTGGATCAC	59349
rs764153272	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202896133	TTGGATTTCCATGTT[A/T]TCTCAGAAATTACTA	59349
rs764170373	snp	A/G	0.000120489	0.0077608	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928455	CTTAATATGCCAAGC[A/G]TCTGATTGCAGCAAG	59349
rs764242619	snp	A/G	0.00010433	0.00722177	intron-variant	KLHL12	GRCh38.p7	1:202893458	ATTAGCAAATGTATG[A/G]TACTAAGCCTAGAAT	59349
rs764261228	snp	C/T	3.32209e-05	0.00407546	intron-variant	KLHL12	GRCh38.p7	1:202911234	TACACACCGTGGATC[C/T]TACTTTTCCAATTAG	59349
rs764324337	snp	A/C	1.64741e-05	0.00286998	missense	KLHL12	GRCh38.p7	1:202918234	AAGAATGAACTCTTC[A/C]TGCTGTACCACTTCA	59349
rs764442253	in-del	-/ATTTT			intron-variant	KLHL12	GRCh38.p7	1:202904370	ATAATTTTGTATATG[-/ATTTT]TTTATTTATTCAAAT	59349
rs764495932	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906854	TTTAGTAGACATGGG[A/G]TTTCACCATGTTGGC	59349
rs764515708	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202914096	AATATGAAGCTGGAG[A/T]GTTAAGCAAGGGCCA	59349
rs764626301	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891433	AGGAAAACTTATAGC[A/G]GAAAAAAGACTAGAT	59349
rs764643744	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202911958	TGTGGTAATGAGAGA[A/C]CCAAACACCAAGTGC	59349
rs764679282	snp	C/G	1.64819e-05	0.00287066	intron-variant	KLHL12	GRCh38.p7	1:202896803	TGATCTGGAGGCAGA[C/G]ACTGAGGACATTTAA	59349
rs764766586	in-del	-/A			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929758	TTTGGAGACTGAAGC[-/A]AGGAAGATTGCTTGA	59349
rs764850717	snp	A/G/T	4.96055e-05	0.00498003	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892518	CACTAGCTCTGGATG[A/G/T]TGCTCCAACAATGGT	59349
rs764908987	snp	A/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929218	ATGTCATACCTTCCT[A/G]ATCTAAAACTGTCCC	59349
rs764910797	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202900978	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	59349
rs764932289	snp	C/T	1.64738e-05	0.00286995	missense	KLHL12	GRCh38.p7	1:202909060	CTCCGAAGTTCAGGC[C/T]TCAGATGAAACTTCT	59349
rs764995481	snp	C/T			intron-variant, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202927160	AGTGCGGCGCGGGGC[C/T]AGCAGGCGGCTCGGG	59349
rs765042033	snp	C/G	1.64795e-05	0.00287045	synonymous-codon	KLHL12	GRCh38.p7	1:202925154	TTTGGGGGCCATAAT[C/G]CCTCCCATAAAGCAG	59349
rs765094063	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902424	AACAGAGCGAGACTC[C/T]GTCCAAAAAAAAAAA	59349
rs765142138	snp	C/T	1.84497e-05	0.00303719	intron-variant	KLHL12	GRCh38.p7	1:202894325	AGTGGTAAATCCTCA[C/T]GCCCATTCCTGGTCG	59349
rs765155347	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202913138	CGCACTATGCTATTT[C/G]AGAAGATATATTTAA	59349
rs765244944	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202899922	ATGTCTGCCTAAAAT[G/T]ACTTCAAGTTGGGAG	59349
rs765321433	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202894098	TCATTTTTACATTAA[C/T]CTACGGTTTGTCCCA	59349
rs765371523	snp	G/T	9.93888e-05	0.00704872	intron-variant	KLHL12	GRCh38.p7	1:202911212	AATCCACCTGTAAAT[G/T]TATAATTACACACCG	59349
rs765401722	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202894151	AGGTCTGACAGCATC[A/G]CCTATTGTCCCCTCC	59349
rs765483737	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202905995	TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGATACG	59349
rs765526918	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202909942	TTATTAAAAAAAACT[A/C]TTCTAAAATTGTCCT	59349
rs765676318	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202904242	CTCCCGATCTCAGGT[G/T]ATCCACCTGCCTCAG	59349
rs765723956	snp	A/G	1.66874e-05	0.0028885	intron-variant	KLHL12	GRCh38.p7	1:202894762	TATCTGCTCAGAATA[A/G]ACAAATTACAGACTA	59349
rs765728680	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202913847	GCTATTTACATTCAC[C/T]GTAATTAAAACTAAA	59349
rs765764310	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202905512	AAAAATCAAAGTAAG[A/C]AAAATGTCTTATCTC	59349
rs765771585	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202911330	ATTTCCCATCTTCCA[G/T]AAATAGCTAGGCTCT	59349
rs765786597	snp	A/G	3.30797e-05	0.00406679	missense	KLHL12	GRCh38.p7	1:202919904	GGTTTCCCCTTCTCT[A/G]AGAGCTGAAAATTCA	59349
rs765884319	snp	A/G	8.24192e-05	0.00641894	synonymous-codon	KLHL12	GRCh38.p7	1:202919774	CAACTGAAGCAGACA[A/G]GCTGCAGGAAGCAGT	59349
rs765898152	snp	A/G	1.65228e-05	0.00287422	intron-variant	KLHL12	GRCh38.p7	1:202897006	AGTTCAGCATCCCTG[A/G]ATGGGTAACTAGTCA	59349
rs765973031	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202904085	GTGCAATGGCACGAT[C/T]TTGGTTCACCACAAT	59349
rs766058465	snp	G/T	3.29484e-05	0.00405871	missense	KLHL12	GRCh38.p7	1:202925135	GAGTATTTGTCATTA[G/T]GTCTTTGGGGGCCAT	59349
rs766067781	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202912765	CTGGAGAGGAGAGCC[A/G]GAGAAGTGACAGGGA	59349
rs766094982	snp	A/G	8.23784e-05	0.00641735	intron-variant	KLHL12	GRCh38.p7	1:202896837	CCCTCCCAACGAATG[A/G]TTTCACCATTATTTA	59349
rs766148239	snp	A/C	3.29516e-05	0.00405891	missense	KLHL12	GRCh38.p7	1:202925011	TCACTACAGGCAGCC[A/C]GCACAATCCGATGGG	59349
rs766250259	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202897501	AGTGCTGGGATTACA[G/T]GTGTGAGTCACTGTG	59349
rs766348045	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202899424	ACATATACACTCACA[C/T]ATAAACCACGGAGTT	59349
rs766399420	snp	A/G	1.71437e-05	0.00292772	intron-variant	KLHL12	GRCh38.p7	1:202893441	CTGGGGAAAATGAAT[A/G]CATTAGCAAATGTAT	59349
rs766428782	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202908648	AGGGGAAGTGAAGAG[A/G]TGGGTGGAAGCATAT	59349
rs766457945	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202920842	ATATTAAAATACAGA[C/T]GTATTTACAGAATAG	59349
rs766492426	snp	A/G	1.65097e-05	0.00287308	stop-gained, intron-variant	KLHL12	GRCh38.p7	1:202893291	CCCCTACATAGCATC[A/G]TGGAGTGGTCATACT	59349
rs766515278	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202893762	AGTTGTGATTATGGT[C/T]CTGAAGCAATTTTTA	59349
rs766546425	in-del	-/T	1.67351e-05	0.00289263	intron-variant	KLHL12	GRCh38.p7	1:202919706	TATTAATTTTCAACC[-/T]TTCCAGGGCTATTTT	59349
rs766654277	in-del	-/TAAG			intron-variant	KLHL12	GRCh38.p7	1:202920761	TCTATACGCCAGGAA[-/TAAG]TAATAGGTAACACCT	59349
rs766654299	snp	A/G	1.66197e-05	0.00288263	missense	KLHL12	GRCh38.p7	1:202894746	CCAGAGACATAGATC[A/G]TATCTGCTCAGAATA	59349
rs766665146	snp	C/G	1.65176e-05	0.00287376	intron-variant	KLHL12	GRCh38.p7	1:202919749	AGCAAGTTTTAATGT[C/G]TGTACCTTTCAACTG	59349
rs766734100	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	KLHL12	GRCh38.p7	1:202894598	CTCAATACCTAGACA[A/G]TAGATCACTCCACTG	59349
rs766739292	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202893886	CTACTCTTTTGTCCT[G/T]ATGCATTAGAGACTT	59349
rs766861946	snp	A/G	1.65658e-05	0.00287795	intron-variant	KLHL12	GRCh38.p7	1:202918407	GGACAGACACAGGCA[A/G]CAAACACTTTAGAAT	59349
rs766887247	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202895460	CCAGACAACAGGAGA[C/G]GTTAAAAACCCTGGT	59349
rs766970061	snp	A/T	1.65693e-05	0.00287826	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892497	CTAACTGTCCACTGG[A/T]CTGGTCACTAGCTCT	59349
rs767019738	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930101	AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG	59349
rs767029819	snp	C/T	1.64958e-05	0.00287187	missense	KLHL12	GRCh38.p7	1:202924982	CCTCACTAGTGAACA[C/T]GGCACAGAAGTAATC	59349
rs767135855	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202914669	TCAGGAGTTTGAGAC[A/G]AGCCTGGCCAAGATG	59349
rs767243939	snp	G/T	1.6617e-05	0.00288239	intron-variant	KLHL12	GRCh38.p7	1:202919924	CTGAAAATTCAAAAG[G/T]TATAAAAGAATGATG	59349
rs767290300	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202922428	AAAAATTAGCCAGGC[A/G]TCAAGGAAAAAAAAA	59349
rs767334505	snp	A/G	6.64132e-05	0.00576213	intron-variant	KLHL12	GRCh38.p7	1:202892672	TATCTGAGTGGGAAA[A/G]AAGCAAAAGAAAGAA	59349
rs767407064	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202924841	GTGGTAGATCTTATC[C/T]AGAATCTGCCAAAAC	59349
rs767472065	in-del	-/CCTAGTT			intron-variant	KLHL12	GRCh38.p7	1:202920981	GTCTCTCCAGGACTA[-/CCTAGTT]CCTATCATCTGTCCT	59349
rs767541754	snp	C/G	1.65143e-05	0.00287348	missense	KLHL12	GRCh38.p7	1:202911185	TGACAGCCTCAAAGA[C/G]TGGCTCTTCAGAATC	59349
rs767599252	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202923850	TCTACACTAAGATGA[C/T]AGAACTAACTAAAAA	59349
rs767628380	in-del	-/A	1.64732e-05	0.0028699	frameshift-variant	KLHL12	GRCh38.p7	1:202925098	TGAGGGAGTTCATTG[-/A]AATTGAGGATGGATT	59349
rs767629892	snp	A/G	1.65179e-05	0.00287379	intron-variant	KLHL12	GRCh38.p7	1:202911036	GGTTTTGGATCCTGA[A/G]AGTGTTGCACTACTT	59349
rs767702820	snp	A/C	4.94515e-05	0.00497225	intron-variant	KLHL12	GRCh38.p7	1:202894566	CATTGAGTTCCCTCC[A/C]ATTCCTGCATCCCAG	59349
rs767797106	snp	A/G	1.6519e-05	0.00287388	intron-variant	KLHL12	GRCh38.p7	1:202918393	TTGTTTCACACCTAG[A/G]ACAGACACAGGCAGC	59349
rs767843978	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202893074	TGGGTGACAGAGCAA[C/T]ACTCTGTCTCTAAAA	59349
rs767885142	snp	C/T	0.000164726	0.0090739	missense	KLHL12	GRCh38.p7	1:202918256	ACCACTTCAGGAAAA[C/T]GCTTCTGGCTAAAAA	59349
rs767896636	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202893600	ATTCCATCTATAAAC[C/G]CTTTGGCTTGGACTT	59349
rs767915255	snp	A/C			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928357	GCAGGGAGCCTGGGA[A/C]TGTATCTACAGCTCG	59349
rs768160708	snp	C/T	1.77855e-05	0.00298202	intron-variant	KLHL12	GRCh38.p7	1:202893224	TTGAGTCTGGATTCG[C/T]TTCTAAATCCTCACC	59349
rs768192806	in-del	-/G	1.6489e-05	0.00287128	intron-variant	KLHL12	GRCh38.p7	1:202896972	GCTCCTGAAGACAAA[-/G]GCAGAAAAAAGATGG	59349
rs768195107	snp	C/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929778	AGATTGCTTGAGCCC[C/T]GAAGTTCGTGACCAG	59349
rs768197068	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202923975	TTATATAATAAACAG[C/T]GATGCACCCACAACT	59349
rs768233955	snp	C/T	1.65217e-05	0.00287412	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202893382	TGTACCATCAAATCC[C/T]CCCACCACATAAATA	59349
rs768252677	snp	A/G	1.6489e-05	0.00287128	missense	KLHL12	GRCh38.p7	1:202911164	TGGCATGCTTCACCC[A/G]GTTGATGACAGCCTC	59349
rs768261962	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202920425	ACTGTTTCCCAGGCT[A/G]GAGTGCAGTGGTGCC	59349
rs768266282	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202918076	CAAAATGCACACTTA[A/G]TTATGAAGCCCTGAT	59349
rs768282709	in-del	-/TAATAAT			intron-variant	KLHL12	GRCh38.p7	1:202899841	AAAAAAAAAAAAAAA[-/TAATAAT]AATAAATAAAAAAAT	59349
rs768323824	snp	C/T	1.64912e-05	0.00287147	missense	KLHL12	GRCh38.p7	1:202918176	AAATCCGTACCTGAA[C/T]TTCGTCGCACTTGAT	59349
rs768366493	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909388	GTATTTCCCATCTAT[C/T]GCAGCGCTTACATTT	59349
rs768414361	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202912467	GACAGCCGTGGTGGT[A/G]GTGGTGGATATGGTG	59349
rs768494700	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904994	AAGAGTCATTATCCT[A/G]GTAGCTGGTTTAGCA	59349
rs768513281	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915951	TAAGTGAACCAACAG[C/T]AAATGCTGAATAAGT	59349
rs768583903	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202898912	ATTGTGTGATTTTAA[A/T]CAGTGATAATGGCAT	59349
rs768599246	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202917226	ATTATTCCTTCTTCC[C/G]CCGCAAGAGACAGGG	59349
rs768701651	in-del	-/GTTCAAGT			intron-variant	KLHL12	GRCh38.p7	1:202921105	ACCTCTGCCTCCCAG[-/GTTCAAGT]GTTCAAGTGTTTCTC	59349
rs768780357	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202926941	TGACCGAGGCCAGAT[A/G]CCCCACCCCACTGCC	59349
rs768857530	in-del	-/TATC			intron-variant	KLHL12	GRCh38.p7	1:202903976	AACCCTTTAACCCTT[-/TATC]TATCTATCTATCTAT	59349
rs769085231	snp	G/T	4.94368e-05	0.00497152	synonymous-codon	KLHL12	GRCh38.p7	1:202909014	TACCAGCTTACCTAG[G/T]CGAGCCCTTGTCCTG	59349
rs769130565	in-del	-/AT			intron-variant	KLHL12	GRCh38.p7	1:202924679	AATCCAATAGCTGAC[-/AT]GTGTGTTTTACTACA	59349
rs769175837	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202922491	AAGAAGATCCAAGAC[-/T]TTTTTTTTTTTTTGA	59349
rs769177103	snp	A/C	6.59435e-05	0.00574172	intron-variant	KLHL12	GRCh38.p7	1:202896964	CTTCATTGGCTCCTG[A/C]AGACAAAGGCAGAAA	59349
rs769262365	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202919972	TAAAGGCAGAATCTC[A/C]TATCTAAGAGCTTAG	59349
rs769267863	in-del	-/CT			intron-variant	KLHL12	GRCh38.p7	1:202903918	CCACTGCTCTTGGCC[-/CT]GTCTCATGCATTCTT	59349
rs769320889	snp	A/C	4.94442e-05	0.00497188	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892625	TGATAGGGTCATAAC[A/C]TTCAATGCTACTTAG	59349
rs769329110	snp	C/T	3.29609e-05	0.00405948	missense	KLHL12	GRCh38.p7	1:202911146	ATTCTTCCCGCTCTT[C/T]CTTGGCATGCTTCAC	59349
rs769356851	snp	A/T	1.66175e-05	0.00288244	intron-variant	KLHL12	GRCh38.p7	1:202924959	GTGTGGGGCTAATTT[A/T]CCACTTACCTCACTA	59349
rs769395775	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202908115	ACCTAGGCTTTTGGA[C/T]AGTGAAGCAAAGAGA	59349
rs769397973	snp	G/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891836	TCAAATAATATACCC[G/T]TCTCAGTCTTCCAGG	59349
rs769453171	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202918596	GCAAGACCTTTACAC[A/C]TGTCTCTGCTTAATC	59349
rs769487910	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202893119	AATAAAAAAAATCAA[A/G]TTGCCACTGGAGATG	59349
rs769501532	snp	A/G	0.000116728	0.00763874	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202895528	CCAGCCTACCTCCCA[A/G]GGTGGTGGCTCCAGC	59349
rs769548541	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202915592	CTGTATAGTTCCAAA[A/T]GAAATGACTTCTATG	59349
rs769641380	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202914252	TAGAACAGTTTAAAG[A/G]GCCAAGAGCTAGAAG	59349
rs769642679	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202916733	TTAGAGGCTTTCTTT[A/G]AATGGTATTGCCTGA	59349
rs769737790	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202911211	GAATCCACCTGTAAA[C/T]GTATAATTACACACC	59349
rs769743265	snp	A/G	1.65119e-05	0.00287327	missense	KLHL12	GRCh38.p7	1:202894704	TAGCGCTCCATACTG[A/G]TGTGACGCCTGCTTC	59349
rs769748536	snp	A/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929409	ATCAACAACAACATT[A/G]AATGTCCATTAATAG	59349
rs769791759	in-del	-/TTC	1.64776e-05	0.00287028	cds-indel	KLHL12	GRCh38.p7	1:202911131	CAGGTTAGGCAAGGA[-/TTC]TTCTTCCCGCTCTTT	59349
rs769829965	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202897086	TGAGGGATGCAATCC[A/G]AAATGGGAGATAATC	59349
rs769833084	snp	A/C	1.66283e-05	0.00288338	intron-variant	KLHL12	GRCh38.p7	1:202919727	GGGCTATTTTGACAT[A/C]AACAATAGCAAGTTT	59349
rs769880715	snp	A/C	1.64779e-05	0.00287031	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896944	GCCCCCAACCACCAA[A/C]AGCACTTCATTGGCT	59349
rs769969524	snp	A/C/T			intron-variant	KLHL12	GRCh38.p7	1:202925975	CCAGGCGTGGTGATG[A/C/T]GCGCCTATAATCCTA	59349
rs770009564	in-del	-/TT			intron-variant	KLHL12	GRCh38.p7	1:202921177	ACTACAACCAGCTAA[-/TT]TTTTTTTTTTTTTTT	59349
rs770168346	in-del	-/TT			intron-variant	KLHL12	GRCh38.p7	1:202919542	GGTGCAAATGCTCTC[-/TT]TTATAGAGCCAAATA	59349
rs770201887	snp	A/T	1.64732e-05	0.0028699	missense	KLHL12	GRCh38.p7	1:202925061	TACTCTCAATGTCAC[A/T]TCACAGAGGGTATTG	59349
rs770278043	snp	C/T	3.29614e-05	0.00405951	missense, intron-variant	KLHL12	GRCh38.p7	1:202893351	TGTTGTATGCTTCAA[C/T]GGAAGAAAGGTGGGC	59349
rs770285405	snp	C/G	6.71987e-05	0.0057961	intron-variant	KLHL12	GRCh38.p7	1:202924939	GAGTTCCACGGGTTT[C/G]ATTTGTGTGGGGCTA	59349
rs770344551	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202898788	GAGACATGAAATCAC[A/G]AGCAACGTGTGGACT	59349
rs770407297	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202906607	TTAACATGAGTCAAC[C/T]GTACATGTAAAAATG	59349
rs770431123	snp	C/T	1.64743e-05	0.00287	missense	KLHL12	GRCh38.p7	1:202909048	CCCTGCATCTGACTC[C/T]GAAGTTCAGGCCTCA	59349
rs770444708	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202905227	TAACCAAGCAGGAGC[C/T]CCTTCTGCTGCCTGT	59349
rs770521328	snp	A/G	1.87954e-05	0.00306551	intron-variant	KLHL12	GRCh38.p7	1:202925221	AACTACAAGAGGGAA[A/G]AAAAAACAATGAGCA	59349
rs770560309	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202904369	ATAATTTTGTATATG[-/A]ATTTTTTTATTTATT	59349
rs770710185	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202892972	GCTTGAGCCCAGGAG[C/T]TGGAGACCAGCCTAG	59349
rs770733365	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202918902	ATGTATTAAAAACTA[A/C]AAGTGTGTCAATTAT	59349
rs770744955	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202918069	TTTGAGCCAAAATGC[A/G]CACTTAATTATGAAG	59349
rs770788218	snp	C/T	1.64866e-05	0.00287106	stop-gained	KLHL12	GRCh38.p7	1:202894668	TCTCCCAGCATGCTC[C/T]ACTGGTCAATGTTTG	59349
rs770805929	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202926323	GGGGGAAGGAAATCA[A/C]ACTGTGGTCTCCAAA	59349
rs770830744	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202914111	AGTTAAGCAAGGGCC[A/C]GGTACAGAGAGCATT	59349
rs770877593	snp	C/G	1.64743e-05	0.00287	missense	KLHL12	GRCh38.p7	1:202918314	AATTGTGGGTTTCAG[C/G]AAAATCCCTAATACC	59349
rs770884383	snp	A/G	0.000177794	0.00942683	intron-variant	KLHL12	GRCh38.p7	1:202894293	TCCTCCTGGAAGACA[A/G]AGACCATTCCAGAAA	59349
rs770944885	snp	A/T	1.72868e-05	0.00293992	intron-variant	KLHL12	GRCh38.p7	1:202895732	TCTATGGATTTGGAG[A/T]GAAGAGGTACAGAGC	59349
rs771036525	snp	A/C/G	0.00011783	0.00767483	intron-variant	KLHL12	GRCh38.p7	1:202924933	CAACTAGAGTTCCAC[A/C/G]GGTTTCATTTGTGTG	59349
rs771066732	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202909763	GTCAAGGTTTCTCTC[A/G]AGGCAGTGACTCTAC	59349
rs771071486	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903729	CTGGGCTAAAATGAT[C/T]CTCCTGCCTCAACCT	59349
rs771074229	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202911749	TTTCAAAAGCATTAT[C/T]GCCTTTCTGCCTGTG	59349
rs771118191	snp	C/G	3.29794e-05	0.00406061	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202895568	TCGGACATTCATAGG[C/G]GCCACAGAATACCAG	59349
rs771228717	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202898390	TACCTTGAAGCTGAC[A/C]GGAAACACAGATAAA	59349
rs771251724	snp	A/T	1.64866e-05	0.00287106	stop-gained	KLHL12	GRCh38.p7	1:202919885	ACCTTGGATGTCAAC[A/T]TAAGGTTTCCCCTTC	59349
rs771314667	snp	A/G	1.6477e-05	0.00287024	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892594	CCCATGGATGTCACG[A/G]CTTCCCAGCTGTCGA	59349
rs771352133	snp	C/T	1.79348e-05	0.00299451	intron-variant	KLHL12	GRCh38.p7	1:202893207	CTTGCTCTGGCTACA[C/T]ATTGAGTCTGGATTC	59349
rs771481964	snp	A/T	1.66286e-05	0.0028834	intron-variant	KLHL12	GRCh38.p7	1:202909161	AGTTAGGCACTGGGG[A/T]TACCTGTAATACTAT	59349
rs771586916	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917290	TGCGATCATGGCTCA[C/T]TGCAGCCTCAAACTC	59349
rs771597257	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202897544	GCACCATTTCAACCT[A/T]TTGAGATGACTGGCT	59349
rs771676740	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202903935	GTCTCATGCATTCTT[A/C]TGAGCTCTTTACACA	59349
rs771680562	snp	A/C	1.65438e-05	0.00287605	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202893388	ATCAAATCCCCCCAC[A/C]ACATAAATATGGTCA	59349
rs771726087	snp	A/G	3.47959e-05	0.00417094	synonymous-codon	KLHL12	GRCh38.p7	1:202894254	GTATTTCTCAACTGA[A/G]TTTAAGATATTCAAG	59349
rs771735163	in-del	-/CCCATTA	1.65051e-05	0.00287267	intron-variant	KLHL12	GRCh38.p7	1:202894542	AATCCTTACCCACAG[-/CCCATTA]CCCATTGAGTTCCCT	59349
rs771829319	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202913253	TCACTGGAAGGACTT[A/C]GGTATATAATAACAC	59349
rs771900812	snp	C/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891547	TAGGCTACTGTCACT[C/G]CCAGCCCATCCCCAA	59349
rs771906559	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	KLHL12	GRCh38.p7	1:202918290	CAGCTGCTTGCATCA[A/G]GTCAACACAATTGTG	59349
rs772082575	snp	A/G	1.65389e-05	0.00287562	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202895547	GGTGGCTCCAGCAAG[A/G]CCTCGTCGGACATTC	59349
rs772172467	snp	A/G	1.65693e-05	0.00287826	missense	KLHL12	GRCh38.p7	1:202894734	CCATCAAAGCCTCCA[A/G]AGACATAGATCATAT	59349
rs772197632	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915124	TCACAAAGAATTCTC[C/T]TGAGTATTAGGTACT	59349
rs772239694	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202902247	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT	59349
rs772260431	snp	A/T	1.65575e-05	0.00287724	intron-variant	KLHL12	GRCh38.p7	1:202919738	ACATAAACAATAGCA[A/T]GTTTTAATGTCTGTA	59349
rs772305070	in-del	-/GGA			intron-variant	KLHL12	GRCh38.p7	1:202906491	AAAGTTCCTACCCTG[-/GGA]GGAGGAAAGGCAAAA	59349
rs772381045	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202895429	CTTAATTTTTTCTCC[A/G]TATTTCATGCTCCTG	59349
rs772389361	in-del	-/TTTTTTTTTTTTT			intron-variant	KLHL12	GRCh38.p7	1:202903616	AGCTGGGACCACTAA[-/TTTTTTTTTTTTT]TTTTTTTCTTTTCTT	59349
rs772397033	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202909628	TCTTTCATTTGCCTC[C/T]CAACTCACTCTGTAC	59349
rs772486643	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202910842	ACAAAATTGAACCAC[A/G]GATTTTCATTTGTGT	59349
rs772507937	snp	C/T	1.6477e-05	0.00287024	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892592	TTCCCATGGATGTCA[C/T]GACTTCCCAGCTGTC	59349
rs772518399	snp	A/G	1.65649e-05	0.00287788	intron-variant	KLHL12	GRCh38.p7	1:202909147	ATAGCAGACAGCAGA[A/G]TTAGGCACTGGGGAT	59349
rs772519697	snp	A/G	1.73375e-05	0.00294422	synonymous-codon, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202925207	TCCTTGGATTCTGCA[A/G]CTACAAGAGGGAAAA	59349
rs772597619	snp	A/T	1.65809e-05	0.00287926	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892485	TTGATTCTCCCACTA[A/T]CTGTCCACTGGACTG	59349
rs772786410	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202918656	ATCCAGAGACCTGGC[A/C]CAATTCAACAAAAAT	59349
rs772795134	snp	A/C	1.64735e-05	0.00286993	missense	KLHL12	GRCh38.p7	1:202925118	GAGGATGGATTTAGC[A/C]TGAGTATTTGTCATT	59349
rs772799894	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202917621	CACTTCCAAACTTTT[C/G]TCTCTTCATTTCTGA	59349
rs772893807	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202926227	GCTCTTCAACAAGAG[A/G]GTATTCCTACTCTAC	59349
rs772899805	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202914866	GCGAAACTCCGTCTA[-/A]AAAAAAAAAAAAAAA	59349
rs772978994	in-del	-/AT			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892434	TGTAATCACCCGGTG[-/AT]CACATAGTGAGAAAC	59349
rs773067521	in-del	-/C			downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890885	CTTTTTCAAGTAACT[-/C]CCAAGCGTCAGAGGG	59349
rs773157193	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202905179	TAGATTTATAGTTTA[A/G]TCCCTTAAGGTCAGG	59349
rs773158440	in-del	-/C	3.3168e-05	0.00407221	intron-variant	KLHL12	GRCh38.p7	1:202911223	AAATGTATAATTACA[-/C]ACCGTGGATCCTACT	59349
rs773312387	snp	G/T	1.6517e-05	0.00287372	synonymous-codon	KLHL12	GRCh38.p7	1:202911186	GACAGCCTCAAAGAC[G/T]GGCTCTTCAGAATCC	59349
rs773316341	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202926156	CCATTACCTACACTG[-/A]AATAATGGAAACCAC	59349
rs773437329	snp	A/G/T	3.29545e-05	0.00405911	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892593	TCCCATGGATGTCAC[A/G/T]ACTTCCCAGCTGTCG	59349
rs773446760	snp	A/G	1.65523e-05	0.00287678	intron-variant	KLHL12	GRCh38.p7	1:202919739	CATAAACAATAGCAA[A/G]TTTTAATGTCTGTAC	59349
rs773637552	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202897776	GGTCTCGCTATATTG[C/T]CCAGGCTGATCTCAA	59349
rs773644046	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202893637	ATAAAAGATAAATAA[C/T]AAAAATGGTTCTCTT	59349
rs773671503	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202908449	ACAGGCAGGTGCTAC[A/G]ATGATTCCATTTACA	59349
rs773701757	snp	A/G	1.65798e-05	0.00287917	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892488	ATTCTCCCACTAACT[A/G]TCCACTGGACTGGTC	59349
rs773746245	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202915964	AGTAAATGCTGAATA[A/C]GTATTAGCTATTATA	59349
rs773919798	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202895343	AGGCTGCAGTGAGCC[A/G]TGATCACACCACTGC	59349
rs773938287	snp	A/C			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929915	TTCGAGAGGCCGAGG[A/C]GGGCGGATCACCTGA	59349
rs774009398	snp	A/T			missense, intron-variant	KLHL12	GRCh38.p7	1:202893252	ACCCTGCAATTGCAT[A/T]GAGTCTCCCCCGAAG	59349
rs774099680	snp	C/G	1.65449e-05	0.00287614	intron-variant	KLHL12	GRCh38.p7	1:202911022	TAAGAGTCCGTCAAG[C/G]TTTTGGATCCTGAGA	59349
rs774101004	snp	A/C	1.76714e-05	0.00297244	intron-variant	KLHL12	GRCh38.p7	1:202893233	GATTCGTTTCTAAAT[A/C]CTCACCCTGCAATTG	59349
rs774193240	snp	C/T	1.64893e-05	0.0028713	missense	KLHL12	GRCh38.p7	1:202911166	GCATGCTTCACCCAG[C/T]TGATGACAGCCTCAA	59349
rs774227881	in-del	-/GTC			intron-variant	KLHL12	GRCh38.p7	1:202904219	ATGTTGGTCAGGCTG[-/GTC]TCAAACTCCCGATCT	59349
rs774230857	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902581	AGGGTTTATAATTTT[A/G]GGTTATAAACAATCA	59349
rs774291134	in-del	-/TTCAGT			intron-variant	KLHL12	GRCh38.p7	1:202896547	CAATTTAACATTCAG[-/TTCAGT]TTAACACAGCACGAC	59349
rs774301036	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202917229	ATTCCTTCTTCCCCC[A/G]CAAGAGACAGGGTCT	59349
rs774318971	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202903873	ATCGCCTGCCTCAGC[C/G]TCTCAAAGTGCTGGG	59349
rs774413122	snp	A/T	1.66015e-05	0.00288105	intron-variant	KLHL12	GRCh38.p7	1:202919731	TATTTTGACATAAAC[A/T]ATAGCAAGTTTTAAT	59349
rs774482678	snp	C/T	1.64942e-05	0.00287173	intron-variant	KLHL12	GRCh38.p7	1:202894551	CCACAGCCCATTACC[C/T]ATTGAGTTCCCTCCC	59349
rs774502549	snp	C/T	1.64768e-05	0.00287021	missense	KLHL12	GRCh38.p7	1:202918346	AGGCAATTAGAAGGG[C/T]CCAACTGACTTTCTA	59349
rs774660269	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202920193	GTGGCACATGCCTGT[A/G]GTCCCAGCTACTCAG	59349
rs774767279	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202913785	CAGACAGAAGAGCAC[A/G]CTAAAAAGCACTAGA	59349
rs774894949	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202921466	AGGCGTGAGCCACCA[C/T]GCCCGGCCCTTAGAC	59349
rs774940977	snp	C/T	1.64822e-05	0.00287068	missense	KLHL12	GRCh38.p7	1:202911152	CCCGCTCTTTCTTGG[C/T]ATGCTTCACCCAGTT	59349
rs774946172	snp	A/T	1.64732e-05	0.0028699	missense	KLHL12	GRCh38.p7	1:202925086	GTATTGCTCTTCCTG[A/T]GGGAGTTCATTGAAT	59349
rs774964356	snp	C/T	0.00010699	0.00731325	intron-variant	KLHL12	GRCh38.p7	1:202893222	TATTGAGTCTGGATT[C/T]GTTTCTAAATCCTCA	59349
rs774997173	snp	C/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927396	AATTACAAAAAGGTC[C/G]GGTGGGCAGGGAATG	59349
rs775023096	snp	A/G	1.64811e-05	0.00287059	intron-variant	KLHL12	GRCh38.p7	1:202896808	TGGAGGCAGAGACTG[A/G]GGACATTTAACATCC	59349
rs775054022	snp	C/T	1.64811e-05	0.00287059	synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892626	GATAGGGTCATAACA[C/T]TCAATGCTACTTAGC	59349
rs775151372	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202902413	CCAGCCTGGGTAACA[A/G]AGCGAGACTCCGTCC	59349
rs775177088	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202903299	TAGTTTTTAAATCTC[-/T]TGACACTCTGGTAGG	59349
rs775204421	snp	A/G	0.000120985	0.00777675	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928443	AGAATTCCAACGCTT[A/G]ATATGCCAAGCATCT	59349
rs775208036	snp	A/C			downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890844	TTCAAGCGCGTGCTA[A/C]GTGAATTCAAGATCT	59349
rs775243684	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202906747	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	59349
rs775278518	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202907511	GGAGTCTGAGGCACA[A/G]GAATTGCTTGAACCT	59349
rs775330084	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202908261	CTCTCATCTTAGTGG[C/T]AGACATACAGGCTCA	59349
rs775332302	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892036	CCTCTAGAATGGAAC[C/T]GTGTTGCCCCTAGCT	59349
rs775369295	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202914257	CAGTTTAAAGGGCCA[A/C]GAGCTAGAAGAGGTT	59349
rs775371725	snp	G/T			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929662	GTAATTTATTTTGCC[G/T]TTTGAATTTTGCTTC	59349
rs775461630	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202915604	AAAAGAAATGACTTC[C/T]ATGATTATTTCCTGA	59349
rs775562645	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202925957	TAAAAATACAAAAAA[A/T]AGCCAGGCGTGGTGA	59349
rs775574151	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202923716	TAAAATGAGATGGTA[A/C]TACCTACCCCTAGGG	59349
rs775605295	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	KLHL12	GRCh38.p7	1:202918219	CTCTCCTTGACTCAG[A/G]AGAATGAACTCTTCA	59349
rs775642018	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202897111	ATAATCATAAGGCTG[C/T]CGAATGGGGAGTTAT	59349
rs775784323	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202903741	GATTCTCCTGCCTCA[A/G]CCTCCCCAATAGCTG	59349
rs775809741	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202898828	TTCTGATTTGAACAA[A/C]ATAAGTACTCAAAAA	59349
rs775820490	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924681	TCCAATAGCTGACAT[A/G]TGTGTTTTACTACAT	59349
rs775908332	snp	C/G/T	3.29594e-05	0.00405941	missense, intron-variant	KLHL12	GRCh38.p7	1:202896949	CAACCACCAAAAGCA[C/G/T]TTCATTGGCTCCTGA	59349
rs775920531	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202919022	CTGGGAGGCAAGGTG[G/T]GAGGATCACTCGAGC	59349
rs775935952	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202920061	GCTCATGCCTGTAAT[A/C]CCAGCACTTTGAGAG	59349
rs775945047	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202913749	GCAGTTAGCCAGGGG[A/G]AGTAAGAGAGTACTC	59349
rs776002316	snp	C/T	1.65658e-05	0.00287795	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892502	TGTCCACTGGACTGG[C/T]CACTAGCTCTGGATG	59349
rs776170141	snp	A/G	3.30896e-05	0.00406739	synonymous-codon	KLHL12	GRCh38.p7	1:202919906	TTTCCCCTTCTCTGA[A/G]AGCTGAAAATTCAAA	59349
rs776206294	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	KLHL12	GRCh38.p7	1:202909053	CATCTGACTCCGAAG[C/T]TCAGGCCTCAGATGA	59349
rs776292447	snp	A/C	1.92158e-05	0.0030996	intron-variant	KLHL12	GRCh38.p7	1:202925226	CAAGAGGGAAAAAAA[A/C]ACAATGAGCATATTC	59349
rs776342696	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202915161	CTTATTTTATGCTCA[G/T]AACAGTCCTGTGTAC	59349
rs776384124	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202918972	AGAAAAACTGGGGAC[C/G]AGGAACGGTGGCTCG	59349
rs776451336	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	KLHL12	GRCh38.p7	1:202918321	GGTTTCAGCAAAATC[C/T]CTAATACCCAGGCAA	59349
rs776474146	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202905232	AAGCAGGAGCCCCTT[C/G]TGCTGCCTGTTCAGA	59349
rs776493002	in-del	-/GA	1.65239e-05	0.00287431	intron-variant	KLHL12	GRCh38.p7	1:202911034	AAGGTTTTGGATCCT[-/GA]GAGTGTTGCACTACT	59349
rs776573740	snp	C/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891729	AGTTATACTGAACTC[C/G]CACATTGATGTCATC	59349
rs776692558	snp	A/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929037	TGTTTCGCCATCTTG[A/G]CCGGGCTGGTCTCGA	59349
rs776692885	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202912964	GGAAAGCGTAAAGCA[C/T]TCCAACAAAGGGTTT	59349
rs776735315	snp	A/G	0.000328342	0.0128087	intron-variant	KLHL12	GRCh38.p7	1:202893451	TGAATGCATTAGCAA[A/G]TGTATGGTACTAAGC	59349
rs776738981	snp	C/T	1.64866e-05	0.00287106	missense, intron-variant	KLHL12	GRCh38.p7	1:202895573	CATTCATAGGGGCCA[C/T]AGAATACCAGACCCC	59349
rs776749632	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202904798	ATAACAGGGTTCAGA[C/G]ACTCACATTTCCATT	59349
rs776876100	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202923208	CATTTCCAAATAACA[A/G]AAGAGTAAAGACACT	59349
rs776924763	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202925590	AATGTCCTTAAGTAG[A/G]TAAGTATTTAGAGCA	59349
rs776929159	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202898493	TATTACTATGAGACA[C/T]TGAGTGCTTCCTAAT	59349
rs776973483	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202923464	ACCTGTCAGGTTCCT[A/G]TTTTCCCTACTAGCC	59349
rs777074398	snp	C/T			missense, intron-variant	KLHL12	GRCh38.p7	1:202895641	CTAAGGCGGGAACGG[C/T]CATCATAGCCACCAA	59349
rs777110286	snp	A/G	1.64923e-05	0.00287156	synonymous-codon	KLHL12	GRCh38.p7	1:202919761	TGTCTGTACCTTTCA[A/G]CTGAAGCAGACAGGC	59349
rs777152960	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917739	AACATTTTTTTTGTC[C/T]ATATCTCTGTCTCTA	59349
rs777162279	snp	A/C	1.65089e-05	0.00287301	intron-variant	KLHL12	GRCh38.p7	1:202896996	AAGATGGGTTAGTTC[A/C]GCATCCCTGGATGGG	59349
rs777234309	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202896484	GTGTGAGCTACCACG[C/T]CCAGCCCAAACTTCT	59349
rs777247548	snp	C/G	1.64765e-05	0.00287019	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892602	TGTCACGACTTCCCA[C/G]CTGTCGATGATAGGG	59349
rs777294317	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202900651	GGTGGATCACTTGAG[A/G]TCAGGAGTTCAAGGC	59349
rs777434651	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202898075	GATAAAATATTTCCT[A/G]CCTTGGCTTTTGGAG	59349
rs777524779	snp	A/C	1.64795e-05	0.00287045	missense	KLHL12	GRCh38.p7	1:202894649	TTCCCGGGCTGTCTG[A/C]ATATCTCCCAGCATG	59349
rs777612953	snp	C/G	1.67142e-05	0.00289081	intron-variant	KLHL12	GRCh38.p7	1:202918433	AGAATAGTTGGACAG[C/G]TGTGATCTAGGATAT	59349
rs777709619	snp	C/T	1.68709e-05	0.00290434	intron-variant	KLHL12	GRCh38.p7	1:202924922	GTGAAATTAGACAAC[C/T]AGAGTTCCACGGGTT	59349
rs777802372	snp	A/G	1.6516e-05	0.00287362	intron-variant	KLHL12	GRCh38.p7	1:202908974	GCAAGAAGTAGTTGA[A/G]AAGCATCCCCTCATT	59349
rs777806542	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202920964	TGTGGGTTATAACTC[C/T]AGTCTCTCCAGGACT	59349
rs777812307	snp	A/G	1.64792e-05	0.00287042	missense, intron-variant	KLHL12	GRCh38.p7	1:202893333	TCCAGGAATCAGTGC[A/G]AATGTTGTATGCTTC	59349
rs777998795	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202925552	ATATAAAATTTCTTA[A/C]AGGTGTTATATTATT	59349
rs778003702	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202915246	TAACACATGCCACCC[A/G]GCCAAGACTAAATCC	59349
rs778072680	snp	C/T	1.65655e-05	0.00287793	intron-variant	KLHL12	GRCh38.p7	1:202909149	AGCAGACAGCAGAGT[C/T]AGGCACTGGGGATAC	59349
rs778107107	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202910884	CTTGCCAAGAAATTC[A/G]CTTTTCTTAGAAATA	59349
rs778115101	in-del	-/A	8.87863e-05	0.00666223	intron-variant	KLHL12	GRCh38.p7	1:202894291	ATCCTCCTGGAAGAC[-/A]AGAGACCATTCCAGA	59349
rs778192190	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202911607	GGGAATCTGTTGCCT[C/T]ATTCGAAGTCAGCTC	59349
rs778204864	in-del	-/C	1.93183e-05	0.00310785	intron-variant	KLHL12	GRCh38.p7	1:202925228	AGAGGGAAAAAAAAA[-/C]AATGAGCATATTCAA	59349
rs778314462	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202920753	GGTAGTTATCTATAC[A/G]CCAGGAATAAGTAAT	59349
rs778392292	snp	C/T			synonymous-codon	KLHL12	GRCh38.p7	1:202925043	AGGGAAGTCTTTCTG[C/T]TCTACTCTCAATGTC	59349
rs778398014	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202924380	TTGTTAGGAGGAGTG[C/G]GATGTGGTTTGAATC	59349
rs778473697	snp	C/T	8.87823e-05	0.00666208	missense	KLHL12	GRCh38.p7	1:202894229	TAGTCCAATGTCCTG[C/T]ATGAGGGTCGTATTT	59349
rs778475908	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202896387	GTAGAGACAGAGTCT[C/T]ACCATATTGCCCAGG	59349
rs778489326	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202924171	AGGCAATTACTAAGT[A/G]GTGTTTCTTAATACT	59349
rs778553825	snp	C/T	6.639e-05	0.00576113	intron-variant	KLHL12	GRCh38.p7	1:202918417	AGGCAGCAAACACTT[C/T]AGAATAGTTGGACAG	59349
rs778559836	snp	A/T	1.64738e-05	0.00286995	missense	KLHL12	GRCh38.p7	1:202918287	CCTCAGCTGCTTGCA[A/T]CAGGTCAACACAATT	59349
rs778670064	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202910801	TATATAAAACACTCA[C/G]AGGCATGTAAAACAG	59349
rs778671020	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202904997	AGTCATTATCCTGGT[A/G]GCTGGTTTAGCAGCC	59349
rs778779595	snp	C/T	1.64727e-05	0.00286986	stop-gained, intron-variant	KLHL12	GRCh38.p7	1:202896867	ACTGGCAAAAAGCTC[C/T]ACTCCTGAGTCTTGG	59349
rs778869552	snp	G/T	3.37405e-05	0.0041072	missense, intron-variant	KLHL12	GRCh38.p7	1:202895711	AACGTCTCTTACGAG[G/T]GATGCTCTATGGATT	59349
rs778930553	snp	C/T			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891743	CCCACATTGATGTCA[C/T]CTTCTCTCATCCCAA	59349
rs778944471	in-del	-/AAAAAAAAAAA			intron-variant	KLHL12	GRCh38.p7	1:202899823	GTAAGACTCCATCTC[-/AAAAAAAAAAA]AAAAAAATAATAATA	59349
rs778958066	snp	G/T	8.23649e-05	0.00641683	missense	KLHL12	GRCh38.p7	1:202925031	AATCCGATGGGCAGG[G/T]AAGTCTTTCTGCTCT	59349
rs779038985	snp	C/T			missense	KLHL12	GRCh38.p7	1:202892651	CTTAGCAGGGAATTA[C/T]CATCATATCTGAGTG	59349
rs779102949	snp	C/T	0.00016503	0.00908228	intron-variant	KLHL12	GRCh38.p7	1:202908980	AGTAGTTGAAAAGCA[C/T]CCCCTCATTCTGCCG	59349
rs779133215	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202915075	CATTAATGCCTCACT[A/T]CAGAGAAAAATAGAT	59349
rs779157649	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926950	CCAGATGCCCCACCC[C/T]ACTGCCAGCCTTCCT	59349
rs779252034	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202923098	CTCTCCTTTGAACAA[G/T]TACTCTCAAAAATAA	59349
rs779349411	in-del	-/TC			intron-variant	KLHL12	GRCh38.p7	1:202911457	ATATATATATATGTA[-/TC]TCTCTCTCTCTCTCT	59349
rs779604147	snp	C/T	6.64717e-05	0.00576467	intron-variant	KLHL12	GRCh38.p7	1:202918166	ACATCAAGACAAATC[C/T]GTACCTGAATTTCGT	59349
rs779717291	in-del	-/AGT	1.64772e-05	0.00287025	cds-indel	KLHL12	GRCh38.p7	1:202894597	ACTCAATACCTAGAC[-/AGT]AGATCACTCCACTGG	59349
rs779795387	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202910560	CACAGGTGGTATATA[C/T]GGTAAAAATTATGAA	59349
rs779928725	snp	A/C/T	5.01948e-05	0.00500952	intron-variant	KLHL12	GRCh38.p7	1:202919952	ATGGTTATAATTCCA[A/C/T]AAGATAAAGGCAGAA	59349
rs779986934	in-del	-/TA			frameshift-variant	KLHL12	GRCh38.p7	1:202909109	CCCTGCATTGTAAAC[-/TA]CAGCGGATGAAAGGC	59349
rs780003210	snp	A/G	1.6666e-05	0.00288664	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202895529	CAGCCTACCTCCCAG[A/G]GTGGTGGCTCCAGCA	59349
rs780065495	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202917862	ATTCTCAATAAATGT[C/T]TGTGAAATGAGTGAA	59349
rs780081659	snp	C/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892449	GCACATAGTGAGAAA[C/G]AGACATTCTGGAAAG	59349
rs780168678	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202896268	CACAGTTCACTGCAA[C/T]CTCGAACTCCTGGGC	59349
rs780265307	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202901755	GTAATTAACTTCCCC[A/G]CAACTGCCAACAGAG	59349
rs780282596	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891513	AAAGAATGGGGCAGT[A/G]ATCAGGTAGCTGAAC	59349
rs780295621	snp	C/T	1.64925e-05	0.00287158	missense	KLHL12	GRCh38.p7	1:202909111	CTGCATTGTAAACTA[C/T]AGCGGATGAAAGGCT	59349
rs780385504	snp	C/T	6.59554e-05	0.00574224	intron-variant	KLHL12	GRCh38.p7	1:202908994	ATCCCCTCATTCTGC[C/T]GAGATACCAGCTTAC	59349
rs780477366	snp	C/G	8.25962e-05	0.00642583	missense, utr-variant-5-prime	KLHL12	GRCh38.p7	1:202925176	ATAAAGCAGTGCGGA[C/G]AAAGAACAAAATGGG	59349
rs780477477	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202926003	CTAGCTACCAAGAAG[C/G]CTGAGGCCCGAGAAT	59349
rs780489091	snp	C/T	9.13784e-05	0.00675876	missense	KLHL12	GRCh38.p7	1:202894202	AACGCTTGGTGGCCA[C/T]TGGTGTAACATTAGT	59349
rs780563439	snp	A/G	1.64732e-05	0.0028699	missense	KLHL12	GRCh38.p7	1:202925069	ATGTCACATCACAGA[A/G]GGTATTGCTCTTCCT	59349
rs780577037	snp	C/G	1.64808e-05	0.00287057	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202893352	GTTGTATGCTTCAAC[C/G]GAAGAAAGGTGGGCT	59349
rs780751635	snp	C/T	1.71187e-05	0.00292559	intron-variant	KLHL12	GRCh38.p7	1:202895504	GATGGAAATAATTGC[C/T]CTGCACATCCAGCCT	59349
rs780850589	snp	A/C	3.2969e-05	0.00405998	missense, intron-variant	KLHL12	GRCh38.p7	1:202895645	GGCGGGAACGGCCAT[A/C]ATAGCCACCAATGAC	59349
rs780957461	in-del	-/AA			intron-variant	KLHL12	GRCh38.p7	1:202914865	AGCGAAACTCCGTCT[-/AA]AAAAAAAAAAAAAAA	59349
rs780973829	snp	C/G			upstream-variant-2KB	KLHL12	GRCh38.p7	1:202929339	ACATATACTCGTGCA[C/G]ATGTAAAACGATGTA	59349
rs781026393	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202894410	TTCCAATAACTCTAA[C/G]AGAAATCTGACATTA	59349
rs781041653	snp	C/G	1.67365e-05	0.00289275	intron-variant	KLHL12	GRCh38.p7	1:202919704	ACTATTAATTTTCAA[C/G]CTTTCCAGGGCTATT	59349
rs781048770	snp	A/C			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892043	AATGGAACTGTGTTG[A/C]CCCTAGCTACCTGTA	59349
rs781115585	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	KLHL12	GRCh38.p7	1:202896905	TTTCTCTACCACATC[A/G]ATGGGAGACTGCTGG	59349
rs781125368	snp	C/T	1.64988e-05	0.00287213	missense	KLHL12	GRCh38.p7	1:202894689	TCAATGTTTGGATCA[C/T]AGCGCTCCATACTGG	59349
rs781202014	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	KLHL12	GRCh38.p7	1:202925055	CTGCTCTACTCTCAA[C/T]GTCACATCACAGAGG	59349
rs781206995	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202911411	AGTCAATTTGGGTTA[-/A]AAAAAAAAATATATA	59349
rs781223963	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202922778	GGCGTGAGCCACCAC[A/G]CCCAGCTGAAGATCC	59349
rs781225987	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202907930	AAAAATAAAATATAG[C/T]GGATAAATCACCATT	59349
rs781255625	snp	A/G	1.6489e-05	0.00287128	missense, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892544	ATGGTCACTTCTCGC[A/G]GAGAACACAAACACC	59349
rs781308655	snp	G/T			intron-variant	KLHL12	GRCh38.p7	1:202904946	GGCTATTTTAACTTG[G/T]CTGTCAATTTAATTT	59349
rs781317380	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202909141	TGAAATATAGCAGAC[A/G]GCAGAGTTAGGCACT	59349
rs781405149	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202913552	TCAGATATGATCCTT[A/G]CTCTTAAATGGGGAG	59349
rs781424433	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202903736	AAAATGATTCTCCTG[A/C]CTCAACCTCCCCAAT	59349
rs781512383	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202898977	TAGAGACACACGTGG[-/A]AGTATGACACATAGG	59349
rs781515333	snp	C/T	3.58539e-05	0.00423387	intron-variant	KLHL12	GRCh38.p7	1:202893209	TGCTCTGGCTACATA[C/T]TGAGTCTGGATTCGT	59349
rs781595002	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202926680	TCCTGCCTCAACACT[C/T]CAAGTCTCAGCATAT	59349
rs781610552	in-del	-/TA			intron-variant	KLHL12	GRCh38.p7	1:202907623	AAAAAGGAAAAAAAT[-/TA]TATATATATATATAT	59349
rs781627618	snp	A/C	1.64803e-05	0.00287052	missense, intron-variant	KLHL12	GRCh38.p7	1:202893345	TGCGAATGTTGTATG[A/C]TTCAACGGAAGAAAG	59349
rs781637499	snp	A/T	1.68046e-05	0.00289862	intron-variant	KLHL12	GRCh38.p7	1:202918149	ATCTTGAAGAAACCA[A/T]AACATCAAGACAAAT	59349
rs781663525	snp	C/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927397	ATTACAAAAAGGTCG[C/G]GTGGGCAGGGAATGG	59349
rs781698548	snp	C/T	3.29571e-05	0.00405924	missense	KLHL12	GRCh38.p7	1:202911139	GGCAAGGATTCTTCC[C/T]GCTCTTTCTTGGCAT	59349
rs781703249	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903416	TTACTTGCCCTTCTG[C/T]GAACTGTACACTCAA	59349
rs781775545	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202921708	TTTAGCTAAGAGAAG[-/A]AATCTTCAATTTTAC	59349
rs796080255	in-del	-/T			intron-variant	KLHL12	GRCh38.p7	1:202912988	GGGTTTTAATGCAGA[-/T]TTTTTTTTTTTTTGG	59349
rs796191275	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202899837	CAAAAAAAAAAAAAA[-/A]AAATAATAATAATAA	59349
rs796211024	in-del	-/CTCT			intron-variant	KLHL12	GRCh38.p7	1:202911476	TCTCTCTCTCTCTCT[-/CTCT]AAGATAGATAGTACC	59349
rs796372930	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202911046	CCTGAGAGTGTTGCA[C/T]TACTTACCTCAGCAT	59349
rs796522776	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202913228	ACACTCTAAAAAAAC[C/T]TACACTACATCACTG	59349
rs796569809	in-del	-/A			intron-variant	KLHL12	GRCh38.p7	1:202899840	AAAAAAAAAAAAAAA[-/A]TAATAATAATAAATA	59349
rs796588127	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202917184	ATGCCTGCCTGGCAC[A/G]GGTAGTATCCCCCTG	59349
rs796591734	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202899844	AAAAAAAAAAAATAA[A/T]AATAATAAATAAAAA	59349
rs796713342	in-del	-/AAA			intron-variant	KLHL12	GRCh38.p7	1:202923872	AACTAAAAAAAAAAC[-/AAA]AAACAAACAAAAAAC	59349

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